US3134668A - Liquid iron-based metal and method of producing same - Google Patents
Liquid iron-based metal and method of producing same Download PDFInfo
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- US3134668A US3134668A US93364A US9336461A US3134668A US 3134668 A US3134668 A US 3134668A US 93364 A US93364 A US 93364A US 9336461 A US9336461 A US 9336461A US 3134668 A US3134668 A US 3134668A
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- nitrogen
- converter
- steel
- metal
- selenium
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- 229910052751 metal Inorganic materials 0.000 title claims description 34
- 239000002184 metal Substances 0.000 title claims description 34
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 title description 30
- 238000000034 method Methods 0.000 title description 27
- 229910052742 iron Inorganic materials 0.000 title description 15
- 239000007788 liquid Substances 0.000 title description 12
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 98
- 229910052757 nitrogen Inorganic materials 0.000 claims description 49
- BUGBHKTXTAQXES-UHFFFAOYSA-N Selenium Chemical compound [Se] BUGBHKTXTAQXES-UHFFFAOYSA-N 0.000 claims description 18
- 229910052711 selenium Inorganic materials 0.000 claims description 18
- 239000011669 selenium Substances 0.000 claims description 18
- 238000007664 blowing Methods 0.000 claims description 12
- 238000010521 absorption reaction Methods 0.000 claims description 11
- 229910052714 tellurium Inorganic materials 0.000 claims description 9
- PORWMNRCUJJQNO-UHFFFAOYSA-N tellurium atom Chemical compound [Te] PORWMNRCUJJQNO-UHFFFAOYSA-N 0.000 claims description 9
- 239000000155 melt Substances 0.000 claims description 6
- 238000004519 manufacturing process Methods 0.000 claims description 4
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims 1
- 229910052700 potassium Inorganic materials 0.000 claims 1
- 239000011591 potassium Substances 0.000 claims 1
- 229910000831 Steel Inorganic materials 0.000 description 37
- 239000010959 steel Substances 0.000 description 37
- 230000000087 stabilizing effect Effects 0.000 description 12
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 9
- 229910052799 carbon Inorganic materials 0.000 description 9
- 239000007789 gas Substances 0.000 description 8
- 239000000463 material Substances 0.000 description 8
- 229910052699 polonium Inorganic materials 0.000 description 7
- HZEBHPIOVYHPMT-UHFFFAOYSA-N polonium atom Chemical compound [Po] HZEBHPIOVYHPMT-UHFFFAOYSA-N 0.000 description 7
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 4
- 229910001338 liquidmetal Inorganic materials 0.000 description 4
- 150000002739 metals Chemical class 0.000 description 4
- 229910052710 silicon Inorganic materials 0.000 description 4
- 239000010703 silicon Substances 0.000 description 4
- 238000005275 alloying Methods 0.000 description 3
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 238000002844 melting Methods 0.000 description 3
- 230000008018 melting Effects 0.000 description 3
- 229910052760 oxygen Inorganic materials 0.000 description 3
- 239000001301 oxygen Substances 0.000 description 3
- 238000009628 steelmaking Methods 0.000 description 3
- 229910001339 C alloy Inorganic materials 0.000 description 2
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 2
- 229910045601 alloy Inorganic materials 0.000 description 2
- 239000000956 alloy Substances 0.000 description 2
- 238000004458 analytical method Methods 0.000 description 2
- 150000001875 compounds Chemical group 0.000 description 2
- 239000012535 impurity Substances 0.000 description 2
- 229910052748 manganese Inorganic materials 0.000 description 2
- 239000011572 manganese Substances 0.000 description 2
- QMQXDJATSGGYDR-UHFFFAOYSA-N methylidyneiron Chemical compound [C].[Fe] QMQXDJATSGGYDR-UHFFFAOYSA-N 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 230000000737 periodic effect Effects 0.000 description 2
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 1
- 229910000640 Fe alloy Inorganic materials 0.000 description 1
- 229910001021 Ferroalloy Inorganic materials 0.000 description 1
- 229910000914 Mn alloy Inorganic materials 0.000 description 1
- 229910001370 Se alloy Inorganic materials 0.000 description 1
- OHKMFOAYJDGMHW-UHFFFAOYSA-N [Si].[Se] Chemical compound [Si].[Se] OHKMFOAYJDGMHW-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000032683 aging Effects 0.000 description 1
- 238000009844 basic oxygen steelmaking Methods 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 238000010622 cold drawing Methods 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 150000002505 iron Chemical class 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
- 230000001590 oxidative effect Effects 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- JPJALAQPGMAKDF-UHFFFAOYSA-N selenium dioxide Chemical compound O=[Se]=O JPJALAQPGMAKDF-UHFFFAOYSA-N 0.000 description 1
- 238000004088 simulation Methods 0.000 description 1
- 239000002893 slag Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- XSOKHXFFCGXDJZ-UHFFFAOYSA-N telluride(2-) Chemical compound [Te-2] XSOKHXFFCGXDJZ-UHFFFAOYSA-N 0.000 description 1
- 238000009617 vacuum fusion Methods 0.000 description 1
- 238000009834 vaporization Methods 0.000 description 1
- 230000008016 vaporization Effects 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
- C21C5/28—Manufacture of steel in the converter
- C21C5/30—Regulating or controlling the blowing
- C21C5/34—Blowing through the bath
Definitions
- This invention relates to the stabilization against an increase in N content of hot liquid iron-based metal in the presence of nitrogen and is particularly concerned with a liquid metal of this type containing a stabilizing element of the group VI-A metals of the periodic system with an atomic number between 32 and 85 in an amount sufiicient to retard the nitrogen absorption rate of the liquid metal.
- the present invention is particularly useful in connection with a solution of iron-based metal in processing in a converter process employed in steelmaking operations.
- air is generally blown through a solution of iron-based hot metal to reduce the amount of impurities present, for instance, carbon, silicon and manganese.
- Nitrogen generally present in air, is consequently brought into contact with the hot metal.
- the nitrogen content of the metal out of the blast furnace is generally low due to the relatively high. amounts e.g. 4 percent of carbon present, however, as the carbon content is reduced during the air blowing operation, the nitrogen content tends to increase as a result of existing temperatures and equilibrium favoring such an increase during the operation.
- steel produced by-a converter process possesses different properties from those of steels produced by other methods, e.g. the open hearth process or the oxygen converter process.
- Tests of the physical properties of converter steel with steel produced by the other processes show a difference in properties that varies with nitrogen content. A strong absorption of nitrogen takes place during the converter process when air is blown through the liquid hot metal.
- typical nitrogen analyses in steel manufactured by the open hearth process range from 0.003 to 0.007 Weight percent nitrogen, but converter steels, steels manufactured by the converter process, show nitrogen contents ranging from 0.010 to 0.030 weight percent.
- the high nitrogen content gives the converter steel greater strength, higher yield limit, greater aging liability, and greater hardness and brittleness as compared with open hearth steels, for instance.
- high nitrogen steel is of some advantage.
- the high nitrogen content is undesirable since it detrimentally affects the properties of the resultant steel, primarily by reducing the ductility of the steel, but also since it can alloy with other elements in the steel.
- a relatively high nitrogen content is of considerable disadvantage.
- a converter steel with a lower nitrogen content than normal exhibiting properties comparable with a high quality open hearth steel can be produced by reducing the nitrogen absorbing properties of a solution of the liquid iron-based metal charge. This is accomplished by adding a group VI-A metal with an atomic weight between 32 and to the charge which reduces the reaction rate between nitrogen and the liquid metal charge.
- a periodic table such as is shown on page 449, Handbook of Chemistry and Physics, fortieth edition, published by Chemical Rubber Publish ing Co., Cleveland, Ohio, may be used for this purpose. Any of the elements, selenium, tellurium, or polonium or any combination thereof can be added to the charge of liquid iron-based metal prior to or early, i.e.
- stabilizing metal i.e. selenium, tellurium, or polonium
- stabilizing metal can be added to the metal charge individually or in mixtures, in pure form as elemental materials, in compotmd form e.g. selenium oxide, selenium telluride and tellurium oxide, or as part of an alloying addition, e.g.
- manganese alloy containing 5 percent selenium, a silicon-selenium alloy, a ferro-alloy containing one or more of the stabilizing elements can take place in the converter unit itself or outside of it in the transfer ladles used to supply material to the converting unit.
- the particular form in which the materials are added to the converter charge is also of relatively little consequence. Loss of stabilizing metal in the charge by vaporization of the stabilizing elements, which are volatile elements having relatively low boiling points, can be minimized by employing the stabilizing element or metal in compound or alloy form.
- the high temperatures involved in converting processes are sufficient to cause decomposition of compounds or solution of alloying stabilizing metals in the solution of hot iron-based charge for' processing to steel, and consequently would not decrease the effectiveness of the stabilizing metal. It is expected that the addition of these materials in any form would permit them to dissolve into the steel bath and exhibit their influence on the nitrogen absorption properties of the liquid metal by markedly decreasing the rate of nitrogen absorption during processing.
- the stabilizing metals of the present invention are incorporated into a solution of iron-based hot metal in stabilizing amounts to retard the nitrogen absorption rate of the iron-based metal for instance, to maintain the nitrogen content in the resulting steel product generally to less than about 0.009, preferably to less than about 0.006, and these amounts will generally range from about 0.01 to 10, preferably 0.05 to 1, Weight percent of selenium, tellurium, and/or polonium.
- the temperatures at which this process will prove feasible are generally overlapping to the range of temperatures used in standard converter practice.
- the rate of absorption of nitrogen into the hot liquid iron-based metal is temperature dependent and increases with increasing temperature. Accordingly, converters operating at lower temperature ranges during the practice of this invention will tend to yield products e.g. steel, with a lower nitrogen content.
- the temperature ranges over which the process is applicable include temperatures generally from the melting point of carbon-saturated iron and iron alloys, about 2000 F., up to and beyond 3200
- the standard operating temperatures employed in converter practices generally range from about 2400 F. to 3000 F. and these temperatures would be quite suitable for practicing the present invention.
- the present invention is applicable in both acid and basic (referring to the lining material and slag used) converter steelmaking processes and may be used in connection with any pneumatic process involving iron-base materials in the liquid state which are contacted with gas phases containing nitrogen for instance, cupola type melting operations and gas-fired furnaces for melting or re fining steel which would include open hearth and electric furnace processes.
- Example I A typical converter heat in which the stabilizing elements of the present invention are used to delay reaction with nitrogen is carried out in the following manner.
- Scrap materials are first charged to a Bessemer converter unit, hot metal is added to the scrap materials in the unit to form a charge, and solid selenium in an amount of approximately of 1 percent is added to the charge.
- the Bessemer converter is returned to a blowing position and the process is started by blowing air through the metal charge out which contains about 0.003 percent nitrogen at this point, for about 15 to 20 minutes to reduee impurities including about 4 percent carbon, 1.5 percent silicon and 0.75 percent manganese.
- the elements manganese, silicon, and carbon are oxidized and reduced in the melt to a suitable end point c.g. less than about 0.5 percent, the metal is poured into a transfer ladle and treated in the same manner as standard converter heats to produce a steel containing less than about 0.006 percent nitrogen.
- Example II The procedure of Example I is followed except 9 percent telluriurn is used instead of the selenium.
- Example Ill The procedure of Example I is followed except 5 percent polonium is used instead of the selenium.
- the reaction rate coefficient which is a measure of the rate at which nitrogen is absorbed by liquid iron is approximately 0.01 cubic centimeter per square centimeter-second.
- the rate coefficient for liquid iron to which 0.5 weight percent selenium had been added measured under precisely the same conditions was 0.0015 cubic centimeter per square centimeter-second.
- a method for producing steel in a converter by contacting a metal melt with air comprising incorporating into the metal molt an element selected from the group consisting of selenium, tellurium and polonium in an amount sufiicient to reduce the rate of nitrogen absorption during the air blowing of the melt in the converter.
- a method of producing steel by blowing air through a metal melt comprising incorporating into the metal melt an element selected from the group consisting of selenium, tellurium and polonium in an amount sufiicient to reduce the rate of nitrogen absorption during the air blowing of the melt.
- step 3 comprising incorporating into the metal melt an element selected from the group consisting of selenium, tellurium and polonium in an amount sufiicient to reduce the rate of nitrogen absorption during the gas blowing of the melt.
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- Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Manufacturing & Machinery (AREA)
- Materials Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Carbon Steel Or Casting Steel Manufacturing (AREA)
Description
United States Patent 3,134,668 LIQUID IRON-BASED METAL AND METHOD OF PRODUCING SAME Robert D. Pehlhe, 1730 lvywood Drive, Ann Arbor,
Web, and Martin Weinstein, 62 Egmont St, Brookline, Mass.
No Drawing. Filed Mar. 6, 1961, Ser. No. 93,364 3 Claims. (Cl. 75-60) This invention relates to the stabilization against an increase in N content of hot liquid iron-based metal in the presence of nitrogen and is particularly concerned with a liquid metal of this type containing a stabilizing element of the group VI-A metals of the periodic system with an atomic number between 32 and 85 in an amount sufiicient to retard the nitrogen absorption rate of the liquid metal.
The present invention is particularly useful in connection with a solution of iron-based metal in processing in a converter process employed in steelmaking operations. In the converter process, air is generally blown through a solution of iron-based hot metal to reduce the amount of impurities present, for instance, carbon, silicon and manganese. Nitrogen, however, generally present in air, is consequently brought into contact with the hot metal. The nitrogen content of the metal out of the blast furnace is generally low due to the relatively high. amounts e.g. 4 percent of carbon present, however, as the carbon content is reduced during the air blowing operation, the nitrogen content tends to increase as a result of existing temperatures and equilibrium favoring such an increase during the operation. Accordingly, steel produced by-a converter process possesses different properties from those of steels produced by other methods, e.g. the open hearth process or the oxygen converter process. Tests of the physical properties of converter steel with steel produced by the other processes show a difference in properties that varies with nitrogen content. A strong absorption of nitrogen takes place during the converter process when air is blown through the liquid hot metal. For instance, typical nitrogen analyses in steel manufactured by the open hearth process range from 0.003 to 0.007 Weight percent nitrogen, but converter steels, steels manufactured by the converter process, show nitrogen contents ranging from 0.010 to 0.030 weight percent.
The high nitrogen content gives the converter steel greater strength, higher yield limit, greater aging liability, and greater hardness and brittleness as compared with open hearth steels, for instance. In certain applications, high nitrogen steel is of some advantage. However, in general the high nitrogen content is undesirable since it detrimentally affects the properties of the resultant steel, primarily by reducing the ductility of the steel, but also since it can alloy with other elements in the steel. In steels prepared for cold drawing or pressing, a relatively high nitrogen content is of considerable disadvantage.
The relatively high nitrogen content in converter steels has presented a problem which is presently unsolved. In one process, a duplex process, air blown converter steel is conveyed to another steel production furnace, generally an open hearth or electric steel furnace, and subjected to further refiningwhich lowers the nitrogen content. Clearly, it would be of great economic advantage if such a duplex process could be avoided, and a steel with low nitrogen content could be produced directly in a converter using air.
Another suggestion has been to enrich the air with oxygen to produce an oxidizing gas with a low nitrogen content. However, this procedure is not particularly successful in reducing the nitrogen content of converter steel. The nitrogen content of a steel which is in equilibrium with a gas phase is directly proportional to the square ice root of the partial pressure of nitrogen in the gas mix ture. In order to prevent the absorption of nitrogen into the steel by lowering the nitrogen content of the gas phase, it is necessary to go to an almost nitrogen free gas, such as is practiced in oxygen steelmaking where pure oxygen is blown on the liquid iron bath.
In accordance with the present invention, a converter steel with a lower nitrogen content than normal exhibiting properties comparable with a high quality open hearth steel can be produced by reducing the nitrogen absorbing properties of a solution of the liquid iron-based metal charge. This is accomplished by adding a group VI-A metal with an atomic weight between 32 and to the charge which reduces the reaction rate between nitrogen and the liquid metal charge. A periodic table such as is shown on page 449, Handbook of Chemistry and Physics, fortieth edition, published by Chemical Rubber Publish ing Co., Cleveland, Ohio, may be used for this purpose. Any of the elements, selenium, tellurium, or polonium or any combination thereof can be added to the charge of liquid iron-based metal prior to or early, i.e. before significant amounts of nitrogen are absorbed, in the course of the blow in the converter process in order that nitrogen pickup is prevented or considerably retarded. It is necessary according to the invention that stabilizing metal, i.e. selenium, tellurium, or polonium, be added to the metal charge prior to the point that appreciable carbon reduction has taken place or, in the case of charges containing high silicon contents, prior to the time that a considerable temperature increase is observed during blowing. The stabilizing metals can be added to the metal charge individually or in mixtures, in pure form as elemental materials, in compotmd form e.g. selenium oxide, selenium telluride and tellurium oxide, or as part of an alloying addition, e.g. manganese alloy containing 5 percent selenium, a silicon-selenium alloy, a ferro-alloy containing one or more of the stabilizing elements. The actual procedure used in making the addition can take place in the converter unit itself or outside of it in the transfer ladles used to supply material to the converting unit.
The particular form in which the materials are added to the converter charge is also of relatively little consequence. Loss of stabilizing metal in the charge by vaporization of the stabilizing elements, which are volatile elements having relatively low boiling points, can be minimized by employing the stabilizing element or metal in compound or alloy form. The high temperatures involved in converting processes are sufficient to cause decomposition of compounds or solution of alloying stabilizing metals in the solution of hot iron-based charge for' processing to steel, and consequently would not decrease the effectiveness of the stabilizing metal. It is expected that the addition of these materials in any form would permit them to dissolve into the steel bath and exhibit their influence on the nitrogen absorption properties of the liquid metal by markedly decreasing the rate of nitrogen absorption during processing.
The stabilizing metals of the present invention are incorporated into a solution of iron-based hot metal in stabilizing amounts to retard the nitrogen absorption rate of the iron-based metal for instance, to maintain the nitrogen content in the resulting steel product generally to less than about 0.009, preferably to less than about 0.006, and these amounts will generally range from about 0.01 to 10, preferably 0.05 to 1, Weight percent of selenium, tellurium, and/or polonium.
The temperatures at which this process will prove feasible are generally overlapping to the range of temperatures used in standard converter practice. The rate of absorption of nitrogen into the hot liquid iron-based metal is temperature dependent and increases with increasing temperature. Accordingly, converters operating at lower temperature ranges during the practice of this invention will tend to yield products e.g. steel, with a lower nitrogen content. The temperature ranges over which the process is applicable include temperatures generally from the melting point of carbon-saturated iron and iron alloys, about 2000 F., up to and beyond 3200 The standard operating temperatures employed in converter practices generally range from about 2400 F. to 3000 F. and these temperatures would be quite suitable for practicing the present invention.
The present invention is applicable in both acid and basic (referring to the lining material and slag used) converter steelmaking processes and may be used in connection with any pneumatic process involving iron-base materials in the liquid state which are contacted with gas phases containing nitrogen for instance, cupola type melting operations and gas-fired furnaces for melting or re fining steel which would include open hearth and electric furnace processes.
The following examples will serve to illustrate the present invention, but they are not to be considered limiting.
Example I A typical converter heat in which the stabilizing elements of the present invention are used to delay reaction with nitrogen is carried out in the following manner. Scrap materials are first charged to a Bessemer converter unit, hot metal is added to the scrap materials in the unit to form a charge, and solid selenium in an amount of approximately of 1 percent is added to the charge. The Bessemer converter is returned to a blowing position and the process is started by blowing air through the metal charge out which contains about 0.003 percent nitrogen at this point, for about 15 to 20 minutes to reduee impurities including about 4 percent carbon, 1.5 percent silicon and 0.75 percent manganese.
The elements manganese, silicon, and carbon are oxidized and reduced in the melt to a suitable end point c.g. less than about 0.5 percent, the metal is poured into a transfer ladle and treated in the same manner as standard converter heats to produce a steel containing less than about 0.006 percent nitrogen.
Example II The procedure of Example I is followed except 9 percent telluriurn is used instead of the selenium.
Example Ill The procedure of Example I is followed except 5 percent polonium is used instead of the selenium.
An experimental result which is of particular significance is the following: The reaction rate coefficient which is a measure of the rate at which nitrogen is absorbed by liquid iron is approximately 0.01 cubic centimeter per square centimeter-second. The rate coefficient for liquid iron to which 0.5 weight percent selenium had been added measured under precisely the same conditions was 0.0015 cubic centimeter per square centimeter-second. This result shows that a selenium content in liquid iron of less than 0.5 weight percent (some selenium was lost by volatilization) absorbs nitrogen at a rate which is lower than the rate in iron not containing selenium by a factor of 67.
In laboratory simulated heats of converter steel which were carried out by blowing a jet of air on the surface of an iron-carbon alloy containing 4.3 weight percent carbon until the carbon had been lowered to the range typical of steels also showed the marked influence of the alloying elements, selenium and tellurium. In one heat, which was typical of the series investigated, one part per thousand by weight (0.1%) of selenium was added to a 40 pound iron-carbon alloy. The carbon content was blown from 4.3 down to a range typical of steel production and the temperature of the melt was observed to go from below 2500" F. to over 2800" F. The time of blowing was approximately 15 minutes. This laboratory simulation very closely approximated the Bessemer converter practice as it is known today. The vacuum-fusion analysis for nitrogen on the heat described above was 0.0024 weight percent, far below the nitrogen content which is typical of good open hearth practice, and about one-tenth of the nitrogen content of typical commercial converter steel.
We claim:
1. In a method for producing steel in a converter by contacting a metal melt with air, the step comprising incorporating into the metal molt an element selected from the group consisting of selenium, tellurium and polonium in an amount sufiicient to reduce the rate of nitrogen absorption during the air blowing of the melt in the converter.
2. In a method of producing steel by blowing air through a metal melt, the step comprising incorporating into the metal melt an element selected from the group consisting of selenium, tellurium and polonium in an amount sufiicient to reduce the rate of nitrogen absorption during the air blowing of the melt.
3. In a method of producing steel by blowing a gas containing oxygen and nitrogen through a metal melt, the step comprising incorporating into the metal melt an element selected from the group consisting of selenium, tellurium and polonium in an amount sufiicient to reduce the rate of nitrogen absorption during the gas blowing of the melt.
References Cited in the file of this patent UNITED STATES PATENTS
Claims (1)
1. IN A METHOD FOR PRODUCING STEEL IN A CONVERTER BY CONTACTING A METAL WITH AIR, THE STEP COMPRISING INCORPORATING INTO THE METAL MELT AN ELEMENT SELECTED FROM THE GROUP CONSISTING OF SELENIUM, TELLURIUM, AND POTASSIUM IN AN AMOUNT SUFFICIENT TO REDUCE THE RATE OF NITROGEN ABSORPTION DURING THE AIR BLOWING OF THE MELT IN THE CONVERTER.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US93364A US3134668A (en) | 1961-03-06 | 1961-03-06 | Liquid iron-based metal and method of producing same |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US93364A US3134668A (en) | 1961-03-06 | 1961-03-06 | Liquid iron-based metal and method of producing same |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US3134668A true US3134668A (en) | 1964-05-26 |
Family
ID=22238511
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US93364A Expired - Lifetime US3134668A (en) | 1961-03-06 | 1961-03-06 | Liquid iron-based metal and method of producing same |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US3134668A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4081270A (en) * | 1977-04-11 | 1978-03-28 | Union Carbide Corporation | Renitrogenation of basic-oxygen steels during decarburization |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2009716A (en) * | 1932-01-14 | 1935-07-30 | Carpenter Steel Co | Free machining structural alloy |
| US2316948A (en) * | 1940-05-18 | 1943-04-20 | Int Nickel Co | Aluminum-treated cast steel |
-
1961
- 1961-03-06 US US93364A patent/US3134668A/en not_active Expired - Lifetime
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2009716A (en) * | 1932-01-14 | 1935-07-30 | Carpenter Steel Co | Free machining structural alloy |
| US2316948A (en) * | 1940-05-18 | 1943-04-20 | Int Nickel Co | Aluminum-treated cast steel |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4081270A (en) * | 1977-04-11 | 1978-03-28 | Union Carbide Corporation | Renitrogenation of basic-oxygen steels during decarburization |
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