US3282679A - Production of alloy steel - Google Patents
Production of alloy steel Download PDFInfo
- Publication number
- US3282679A US3282679A US304683A US30468363A US3282679A US 3282679 A US3282679 A US 3282679A US 304683 A US304683 A US 304683A US 30468363 A US30468363 A US 30468363A US 3282679 A US3282679 A US 3282679A
- Authority
- US
- United States
- Prior art keywords
- blowing
- slag
- alloy
- iron
- phase
- 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.)
- Expired - Lifetime
Links
- 238000004519 manufacturing process Methods 0.000 title claims description 7
- 229910000851 Alloy steel Inorganic materials 0.000 title description 3
- 239000002893 slag Substances 0.000 claims description 48
- 238000007664 blowing Methods 0.000 claims description 44
- 229910045601 alloy Inorganic materials 0.000 claims description 31
- 239000000956 alloy Substances 0.000 claims description 31
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 28
- 238000000034 method Methods 0.000 claims description 25
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 20
- 229910052799 carbon Inorganic materials 0.000 claims description 20
- 229910052710 silicon Inorganic materials 0.000 claims description 15
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims description 14
- 239000000969 carrier Substances 0.000 claims description 14
- 229910052742 iron Inorganic materials 0.000 claims description 14
- 239000010703 silicon Substances 0.000 claims description 14
- 239000003638 chemical reducing agent Substances 0.000 claims description 13
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 claims description 12
- 229910052804 chromium Inorganic materials 0.000 claims description 12
- 239000011651 chromium Substances 0.000 claims description 12
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 11
- 229910052760 oxygen Inorganic materials 0.000 claims description 11
- 239000001301 oxygen Substances 0.000 claims description 11
- 239000007787 solid Substances 0.000 claims description 11
- 239000007788 liquid Substances 0.000 claims description 8
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 claims description 6
- 229910052750 molybdenum Inorganic materials 0.000 claims description 6
- 239000011733 molybdenum Substances 0.000 claims description 6
- 239000013067 intermediate product Substances 0.000 claims description 5
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N iron oxide Inorganic materials [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 claims description 5
- 229910001220 stainless steel Inorganic materials 0.000 claims description 5
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims description 4
- 239000000470 constituent Substances 0.000 claims description 4
- 229910052698 phosphorus Inorganic materials 0.000 claims description 4
- 239000011574 phosphorus Substances 0.000 claims description 4
- 239000010935 stainless steel Substances 0.000 claims description 4
- 229910000805 Pig iron Inorganic materials 0.000 claims description 3
- LIKBJVNGSGBSGK-UHFFFAOYSA-N iron(3+);oxygen(2-) Chemical compound [O-2].[O-2].[O-2].[Fe+3].[Fe+3] LIKBJVNGSGBSGK-UHFFFAOYSA-N 0.000 claims 1
- 229910000831 Steel Inorganic materials 0.000 description 16
- 239000010959 steel Substances 0.000 description 16
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 10
- 239000000155 melt Substances 0.000 description 10
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 6
- 238000007792 addition Methods 0.000 description 6
- 229910052748 manganese Inorganic materials 0.000 description 6
- 239000011572 manganese Substances 0.000 description 6
- 229910000604 Ferrochrome Inorganic materials 0.000 description 4
- 229910052759 nickel Inorganic materials 0.000 description 4
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 3
- 229910000599 Cr alloy Inorganic materials 0.000 description 3
- 235000011941 Tilia x europaea Nutrition 0.000 description 3
- 229910052782 aluminium Inorganic materials 0.000 description 3
- 239000000788 chromium alloy Substances 0.000 description 3
- 239000004571 lime Substances 0.000 description 3
- 229910000519 Ferrosilicon Inorganic materials 0.000 description 2
- 238000005275 alloying Methods 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- 208000001848 dysentery Diseases 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- NDLPOXTZKUMGOV-UHFFFAOYSA-N oxo(oxoferriooxy)iron hydrate Chemical compound O.O=[Fe]O[Fe]=O NDLPOXTZKUMGOV-UHFFFAOYSA-N 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 229910004709 CaSi Inorganic materials 0.000 description 1
- 229910005347 FeSi Inorganic materials 0.000 description 1
- 229910001182 Mo alloy Inorganic materials 0.000 description 1
- 229910000990 Ni alloy Inorganic materials 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 239000005864 Sulphur Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 239000001996 bearing alloy Substances 0.000 description 1
- OSMSIOKMMFKNIL-UHFFFAOYSA-N calcium;silicon Chemical compound [Ca]=[Si] OSMSIOKMMFKNIL-UHFFFAOYSA-N 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 238000000151 deposition Methods 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 229910000514 dolomite Inorganic materials 0.000 description 1
- 239000010459 dolomite Substances 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 238000011946 reduction process Methods 0.000 description 1
- 238000010079 rubber tapping Methods 0.000 description 1
- 238000005070 sampling Methods 0.000 description 1
- 238000003756 stirring 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
- C21C5/00—Manufacture of carbon-steel, e.g. plain mild steel, medium carbon steel or cast steel or stainless steel
- C21C5/005—Manufacture of stainless steel
Definitions
- This invention is concerned with a further development of this process, and aims at improving the economy of the process by the use of cheap charge materialfor example, of the steelworks own return scrap. Further aims of the invention are to improve the reliability of the analytical composition of steels produced and to produce high alloy steels, that is steels having a content of more than 5% of alloy elements, for example stainless steels, more economically than hitherto.
- stainless steel is made from liquid crude iron and solid alloy carriers and the liquid part of the charge which forms between 20% and 75% by weight of the total charge is first charged into the blowing crucible and is blown in a first blowing phase beneath a highly basic slag, which is rich in ferric oxide to yield an intermediate product having a phosphorus content of less than 0.025%.
- the slag is then removed and a main part of the solid alloy carriers, which are relatively non-oxidising (e.g.
- nickel or molybdenum alloys when compared to the alloy of another part of the carriers are added to the crucible together with chemical heat carriers such as ferro-silicon if required, after which the blowing is continued in the second phase until the solids are liquified and preferably until the required carbon content is reached and then the other part of the solid alloy carriers which are relatively oxidising (e.g. chromium alloys, preferably ferro-chromium) and contain silicon and carbon, are added and blowing is continued in a third blowing phase beneath a new basic slag having a CaO/Si0 ratio of at least 2.5 or a (CaO-i-MgO)/Si0 ratio of at least 1.5,.
- chemical heat carriers such as ferro-silicon if required
- the slag is treated with reducing agents to reduce the slagged alloy constituents and finally, after removal of the reduced slag, the remainder of the alloy carriers of high quality are added to the crucible.
- blowing is performed to start with at a normal blowing energy corresponding to a lance interval of approximately 90 to 140' cm. and a blast pressure of 6 to atm. g.
- the blowing is subsequently continued during the second half of this phase with application of low blowing energy corresponding to a lance interval from 200 to 350 cm. and a blast pressure from 3 to 8 atm.
- the basicity of the slag in the first phase (CaO/SiO should be more than 3.
- the relatively non-oxidising alloys such as nickel and molybdenum, preferably in the form of high alloy scrap, are added to the melt up to 30% by weight of the total quantity of alloy carriers.
- the liquid charge pig-iron or hot air cupola furnace iron
- chemical heat carriers may also be added to the melt. The latter are however necessary only in exceptional cases.
- the manganese content of the melt is also preferably increased before the start of the second blowing phase by the introduction of relatively non-oxidising manganese carriers.
- fresh slag formers may be added to the charge before starting the second blowing phase.
- the metallurgical functions of the second slag are slight, so that the quantity of slag may be kept small.
- the quantity of these slag formers should be approximately 1 to 4%, and the basicity of the slag should not fall below 2.
- the second blowing phase is performed with a normal lance interval and oxygen pressurefor example, with a lance interval of to cm. and a pressure of 6 to 10 atm. g. It continues at least until the metallic charge is thoroughly liquefied, and preferably until the carbon content desired in the finished steel is attained.
- the readily oxidising alloy carriers are added to the melt.
- any type of chromium alloy may be used.
- Ferrochromium alloys containing at least 5% silicon and 5% carbon are preferred.
- the chromium contained in such a material is far cheaper than in normal ferro-chrornium, and the necessary heat carriers in the form of silicon and carbon are also inserted into the melt at no cost. The latter elements are effective during the entire third blowing phase which follows.
- the chromium content of the melt at the end of the second blowing phase is adjusted to be in accordance with the chromium and carbon contents desired in the finished steel and so that the chromium content is higher by 1 to 3% (absolute) than the chromium content in the finished steel. It is advantageous simultaneously to adjust the manganese content of the charge to the upper limit of the finished steel.
- new basic slag formers are added to the charge thus prepared. Their quantity depends upon the SiO produced during the third blowing phase. The basicity (CaO/SiO of the slag produced should not fall below the value 2.5. For steels which must be blown to extremely low carbon contents, it is appropriate, in preparing the crucible to replace a portion of the lime by dolomite; in this case, the slag ratio (CaO+MgO)/Si0 may be lowered to the value 1.5.
- the lance interval which is below normal or else to use a lance which generates a more compact oxygen jet than is otherwise customary.
- the choice of the quantity of oxygen to be blown per unit of time is dependent upon the lump size and composition of the ferro-chromium added. The latter dissolves continuously. By an appropriate control of the oxygen supply, it should be ensured that the active oxygen is only equal in quantity to that required for the combustion of the carbon and silicon liberated.
- the blowing is performed to a carbon content which is below the carbon content prescribed for the finished steel.
- the crucible After completing the blowing, the crucible is tilted. In this position, reducing agents in the form of for example Al, Si or CaSi, are applied to the slag present on the charge in order to reduce oxidised chromium and manganese.
- the proportion of reducing agents depends upon the level of the preceding addition of chromium, and upon the carbon content of the bath. It may be determined empirically for each individual case.
- the addition of the reducing agent may also be performed through a chute or the like with the vessel upright or obliquely positioned.
- oxygen is preferably blown onto the bath for approximately 1 minute with a reduced lance interval and a reduced oxygen supply, in order to accelerate the progress of the slag reduction by mechanical turbulence.
- the reduction process is usually complete after 5 to minutes.
- the crucible is tilted back into the horizontal position, a sample is taken, and a portion of the slag is removed by vigorous letting off. Not later than 5 minutes after the sampling, the crucible is positioned obliquely and 10 to 40% according to the temperature of return scrap, of the same or of a similar quality to the steel to be manufactured is added. Owing to the poor thermal conductivity of the high alloy steels, the heat losses in the stationary bath are low, as the thermal content of the melt is fully sufficient to dissolve the added scrap. Neither the iron content nor the alloy content of the scrap sufiers losses during its dissolution.
- the crucible After adding the scrap, the crucible is restored into the horizontal position and the residue of the slag is removed.
- the further treatment is governed by the quality of steel desired.
- slag formers e.g., in the form of lime and ingot iron, which can be heated with gas burners or oil burners.
- a preferred example of the invention consists in the treatment of the fining slag with reducing agents.
- a white disintegrating slag is produced which causes a difiusion deoxidation and a vigorous disulphurisation.
- the steel may also be deoxidised with aluminum or silicon in a conventional manner.
- the sulphur content of the steel is also reduced to approximately 0.004%.
- a process for the production of stainless steel from crude iron and solid alloy carrier consisting at least in part of chromium, nickel and molybdenum by oxygen top blowing said process including the steps of charging liquid crude iron, which forms between 20% and 75% by weight of the total charge, into a blowing crucible, said crude iron being selected from the group consisting of pig iron and hot air cupola furnace iron, blowing said liquid crude iron in a first blowing phase beneath a highly basic slag, which is rich in ferric oxide, to yield an intermediate product having a phosphorus content of less than 0.025%, removing said slag, adding a main portion of solid alloy carrier bearing nickel and molybdenum together with a heat carrier to said crucible, continuing blowing said charge in a second phase until said main portion of solid alloy carriers is liquefied, and a predetermined carbon content is reached adding another portion of alloy carrier bearing chromium, silicon and carbon, continuing blowing in a third blowing phase beneath a new basic slag having a CaO
Landscapes
- Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Manufacturing & Machinery (AREA)
- Materials Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Treatment Of Steel In Its Molten State (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| AT742062A AT237000B (de) | 1962-09-18 | 1962-09-18 | Verfahren zur Herstellung von legiertem Stahl |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US3282679A true US3282679A (en) | 1966-11-01 |
Family
ID=3595869
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US304683A Expired - Lifetime US3282679A (en) | 1962-09-18 | 1963-08-26 | Production of alloy steel |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US3282679A (de) |
| AT (1) | AT237000B (de) |
| DE (1) | DE1433535A1 (de) |
| GB (1) | GB1025230A (de) |
| LU (1) | LU44082A1 (de) |
| SE (1) | SE305661B (de) |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3751242A (en) * | 1969-04-02 | 1973-08-07 | Eisenwerk Gmbh Sulzbach Rosenb | Process for making chrimium alloys |
| US3773496A (en) * | 1970-02-18 | 1973-11-20 | Maximilianshuette Eisenwerk | Process for producing chrome steels and a converter for carrying out the process |
| DE2428465A1 (de) * | 1973-06-18 | 1975-01-09 | Allegheny Ludlum Ind Inc | Verfahren zum herstellen von rostfreiem stahl |
| US3867133A (en) * | 1973-03-23 | 1975-02-18 | Kawaguchi Seiko Kabushiki Kais | Refining process for removing Mo from high-Ni and/or high-Co, Mo-containing alloy steels |
| US4643766A (en) * | 1985-03-20 | 1987-02-17 | 501 Societe Lorraine de Laminage & Continu -Sollac- | Process for refining phosphoric pig iron |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH07100807B2 (ja) * | 1988-02-24 | 1995-11-01 | 川崎製鉄株式会社 | 低s含クロム溶鉄の製造方法 |
| DE10215828B4 (de) * | 2002-04-10 | 2007-08-02 | Sms Demag Ag | Verfahren und Einrichtung zum Erzeugen von nichtrostendem Stahl, insbesondere von chrom- oder chromnickelhaltigem Edelstahl |
| DE10215839A1 (de) * | 2002-04-10 | 2003-11-06 | Sms Demag Ag | Verfahren und Einrichtung zum Erzeugen von C-Stählen oder nichtrostenden Stählen durch Frischen von phosphorreichem Roheisen im Elektrolichtbogen-Ofen oder im Konverter-Gefäß |
Citations (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US1809436A (en) * | 1927-02-26 | 1931-06-09 | Stainless Steel Corp | Process of purifying metals |
| US1809437A (en) * | 1927-09-15 | 1931-06-09 | Stainless Steel Corp | Stainless chromium alloy and method of producing same |
| US2303064A (en) * | 1939-06-23 | 1942-11-24 | Electro Chimie Metal | Process for simultaneously dephosphorizing and deoxidizing steel |
| US2557458A (en) * | 1950-03-31 | 1951-06-19 | United States Steel Corp | Method of fusing alloy additions to a steel bath |
| US2853377A (en) * | 1954-11-25 | 1958-09-23 | Stora Kopparbergs Bergslags Ab | Two step refining process in a tiltable rotary furnace |
| US2893861A (en) * | 1957-05-10 | 1959-07-07 | Bot Brassert Oxygen Technik A | Method of refining crude iron |
| GB858377A (en) * | 1958-02-12 | 1961-01-11 | Arbed | Improvements relating to the manufacture of steel |
| US3004847A (en) * | 1957-12-23 | 1961-10-17 | Bot Brassert Oxygen Technik Ag | Refining of crude iron |
-
1962
- 1962-09-18 AT AT742062A patent/AT237000B/de active
- 1962-11-16 DE DE19621433535 patent/DE1433535A1/de active Pending
-
1963
- 1963-07-17 LU LU44082D patent/LU44082A1/xx unknown
- 1963-08-14 GB GB32154/63A patent/GB1025230A/en not_active Expired
- 1963-08-21 SE SE9141/63A patent/SE305661B/xx unknown
- 1963-08-26 US US304683A patent/US3282679A/en not_active Expired - Lifetime
Patent Citations (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US1809436A (en) * | 1927-02-26 | 1931-06-09 | Stainless Steel Corp | Process of purifying metals |
| US1809437A (en) * | 1927-09-15 | 1931-06-09 | Stainless Steel Corp | Stainless chromium alloy and method of producing same |
| US2303064A (en) * | 1939-06-23 | 1942-11-24 | Electro Chimie Metal | Process for simultaneously dephosphorizing and deoxidizing steel |
| US2557458A (en) * | 1950-03-31 | 1951-06-19 | United States Steel Corp | Method of fusing alloy additions to a steel bath |
| US2853377A (en) * | 1954-11-25 | 1958-09-23 | Stora Kopparbergs Bergslags Ab | Two step refining process in a tiltable rotary furnace |
| US2893861A (en) * | 1957-05-10 | 1959-07-07 | Bot Brassert Oxygen Technik A | Method of refining crude iron |
| US3004847A (en) * | 1957-12-23 | 1961-10-17 | Bot Brassert Oxygen Technik Ag | Refining of crude iron |
| GB858377A (en) * | 1958-02-12 | 1961-01-11 | Arbed | Improvements relating to the manufacture of steel |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3751242A (en) * | 1969-04-02 | 1973-08-07 | Eisenwerk Gmbh Sulzbach Rosenb | Process for making chrimium alloys |
| US3773496A (en) * | 1970-02-18 | 1973-11-20 | Maximilianshuette Eisenwerk | Process for producing chrome steels and a converter for carrying out the process |
| US3867133A (en) * | 1973-03-23 | 1975-02-18 | Kawaguchi Seiko Kabushiki Kais | Refining process for removing Mo from high-Ni and/or high-Co, Mo-containing alloy steels |
| DE2428465A1 (de) * | 1973-06-18 | 1975-01-09 | Allegheny Ludlum Ind Inc | Verfahren zum herstellen von rostfreiem stahl |
| US4643766A (en) * | 1985-03-20 | 1987-02-17 | 501 Societe Lorraine de Laminage & Continu -Sollac- | Process for refining phosphoric pig iron |
Also Published As
| Publication number | Publication date |
|---|---|
| SE305661B (de) | 1968-11-04 |
| LU44082A1 (de) | 1963-09-17 |
| GB1025230A (en) | 1966-04-06 |
| DE1433535A1 (de) | 1969-03-27 |
| AT237000B (de) | 1964-11-25 |
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