US2207282A - Method of treating alloys - Google Patents
Method of treating alloys Download PDFInfo
- Publication number
- US2207282A US2207282A US252070A US25207039A US2207282A US 2207282 A US2207282 A US 2207282A US 252070 A US252070 A US 252070A US 25207039 A US25207039 A US 25207039A US 2207282 A US2207282 A US 2207282A
- Authority
- US
- United States
- Prior art keywords
- silicon
- slag
- carbon
- alloys
- alloy
- 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
- 229910045601 alloy Inorganic materials 0.000 title description 16
- 239000000956 alloy Substances 0.000 title description 16
- 238000000034 method Methods 0.000 title description 8
- 239000002893 slag Substances 0.000 description 15
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 14
- 229910052799 carbon Inorganic materials 0.000 description 14
- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 description 8
- 229910010271 silicon carbide Inorganic materials 0.000 description 8
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 7
- 229910021332 silicide Inorganic materials 0.000 description 7
- 229910052710 silicon Inorganic materials 0.000 description 7
- 239000010703 silicon Substances 0.000 description 7
- 229910000676 Si alloy Inorganic materials 0.000 description 5
- FVBUAEGBCNSCDD-UHFFFAOYSA-N silicide(4-) Chemical compound [Si-4] FVBUAEGBCNSCDD-UHFFFAOYSA-N 0.000 description 5
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 229910000519 Ferrosilicon Inorganic materials 0.000 description 1
- 229910000720 Silicomanganese Inorganic materials 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 239000011651 chromium Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 229910052742 iron Inorganic materials 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
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- SNICXCGAKADSCV-UHFFFAOYSA-N nicotine Chemical compound CN1CCCC1C1=CC=CN=C1 SNICXCGAKADSCV-UHFFFAOYSA-N 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 229910052814 silicon oxide Inorganic materials 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 229910052720 vanadium Inorganic materials 0.000 description 1
- GPPXJZIENCGNKB-UHFFFAOYSA-N vanadium Chemical compound [V]#[V] GPPXJZIENCGNKB-UHFFFAOYSA-N 0.000 description 1
- 229910052726 zirconium Inorganic materials 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C28/00—Alloys based on a metal not provided for in groups C22C5/00 - C22C27/00
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22B—PRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
- C22B9/00—General processes of refining or remelting of metals; Apparatus for electroslag or arc remelting of metals
- C22B9/10—General processes of refining or remelting of metals; Apparatus for electroslag or arc remelting of metals with refining or fluxing agents; Use of materials therefor, e.g. slagging or scorifying agents
Definitions
- master alloys containing no more than the commercially practicable min imum of carbon.
- Such master alloys include those containing one or more of the elements manganese, vanadium, titanium, chromium, and zirconium, usually with some iron or, less frequently, with nickel or copper.
- One method of producing master alloys of this kind involves the reaction of an ore or an oxydic compound with a low-carbon silicide or high silicon alloy, for instance ferro-silicon or silicomanganese, whereby the silicon is eliminated without introducing any substantial further amount of carbon.
- a low-carbon silicide or high silicon alloy for instance ferro-silicon or silicomanganese
- the carbon content of the product is determined almost entirely by the carbon content of the silicide or high-silicon alloy. Accordingly, it is important that silicides and high-silicon alloys containing the lowest possible percentages of carbon be made available at a reasonable cost, and such is the principal object of this invention.
- the usual commercial methods of making silicides and high-silicon alloys yield products containing small but substantial amounts of carbon, from say 0.1% to 1% or more.
- One well known method comprises the simultaneous reduction of ore and silica with carbon in an electric furnace, the silicon thereby introduced into the product being relied upon to minimize the contamination of the product by carbon derived from that in the original furnace charge.
- the ingredients of the charge are so proportioned that the product contains about 40% to 551% silicon, al- 35 though on occasion the proportion of this element may be as low as 15% or 20% or as high as 60% v. silicon products contain substantial amounts of carbon.
- the invention has many advantages including the ability consistently to produce material of extremely low carbon content from material containing even large amounts of silicon carbide.
- a bath of the molten silicide or high-silicon alloy is maintained molten in the presence of a molten slag having a property of dissolving or trapping silicon carbide.
- Molten slag may be added to molten alloy as the latter comes from the furnace, or the alloy and slag may suitably be heated in, an electric furnace, preferably as a shallow pool to permit ready and rapid exposure of all portions of the pool to the slag.
- the treatment may be continued until 5 substantially all of the silicon carbide enters the slag, and the slag may then be separated from the silicide or alloy.
- the proportion of slag to metal is not critical.
- a satisfactory ratio that is suggested as 'an ex- 25 ample is one part of slag to ten parts of metal, by weight. Such a proportion of slag is adequate without unduly burdening the furnace with an excess volume of slag.
- the op- 30 timum time will depend upon the design of the furnace, the compositions of the various materials involved, and upon various other factors. It has been found that about 45 to 60 minutes is adequate for the treatment of 5000 pounds of molten metal with 500 pounds of slag in an open are electric furnace of the tilting type widely used for making steel.
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Manufacturing & Machinery (AREA)
- Carbon And Carbon Compounds (AREA)
Description
Patented July 9, 1940 UNITED STATES METHOD OF TREATING ALLOYS Joseph H. Brennan, Niagara Falls, N. Y., assignor to Electro Metallurgical Company, a corporation of West Virginia No Drawing. Application January 21, 1939, Serial No. 252,070
2 Claims.
For the production of various useful alloys there is a demand for master alloys containing no more than the commercially practicable min imum of carbon. Such master alloys include those containing one or more of the elements manganese, vanadium, titanium, chromium, and zirconium, usually with some iron or, less frequently, with nickel or copper.
One method of producing master alloys of this kind involves the reaction of an ore or an oxydic compound with a low-carbon silicide or high silicon alloy, for instance ferro-silicon or silicomanganese, whereby the silicon is eliminated without introducing any substantial further amount of carbon. In such methods, the carbon content of the product is determined almost entirely by the carbon content of the silicide or high-silicon alloy. Accordingly, it is important that silicides and high-silicon alloys containing the lowest possible percentages of carbon be made available at a reasonable cost, and such is the principal object of this invention.
The usual commercial methods of making silicides and high-silicon alloys yield products containing small but substantial amounts of carbon, from say 0.1% to 1% or more. One well known method comprises the simultaneous reduction of ore and silica with carbon in an electric furnace, the silicon thereby introduced into the product being relied upon to minimize the contamination of the product by carbon derived from that in the original furnace charge. Usually, the ingredients of the charge are so proportioned that the product contains about 40% to 551% silicon, al- 35 though on occasion the proportion of this element may be as low as 15% or 20% or as high as 60% v. silicon products contain substantial amounts of carbon.
I have observed that a very substantial part of the carbon in alloys of this description exists as silicon carbide, and I have discovered that all but the slightest traces of this silicon carbide can be removed by a relatively simple treatment.
The invention has many advantages including the ability consistently to produce material of extremely low carbon content from material containing even large amounts of silicon carbide.
According to the invention, a bath of the molten silicide or high-silicon alloy is maintained molten in the presence of a molten slag having a property of dissolving or trapping silicon carbide. Molten slag may be added to molten alloy as the latter comes from the furnace, or the alloy and slag may suitably be heated in, an electric furnace, preferably as a shallow pool to permit ready and rapid exposure of all portions of the pool to the slag. The treatment may be continued until 5 substantially all of the silicon carbide enters the slag, and the slag may then be separated from the silicide or alloy.
Almost any slag may be used which is fairly fluid at temperatures in the neighborhood of the -10 melting point of the alloys, which is not too heavily charged with silicon carbide, which does not severely attack the furnace lining, and which does not too rapidly oxidize the valuable constituents of the alloy. Slags of the following re- 15 spective approximate analyses have been used successfully and are disclosed as typical examples:
(1) 49.4% S102, 18.2% A1203, 21.6% CaO, 9.6% MgO, with an acid-to-base ratio of 1.6;
(2) 33.4% SiOz, 27.0% A1203, 23.8% CaO, 15.6%
MgO, with an acid-to-base ratio of 1.0.
The proportion of slag to metal is not critical.
A satisfactory ratio that is suggested as 'an ex- 25 ample is one part of slag to ten parts of metal, by weight. Such a proportion of slag is adequate without unduly burdening the furnace with an excess volume of slag.
Nor is the time of treatment critical. The op- 30 timum time will depend upon the design of the furnace, the compositions of the various materials involved, and upon various other factors. It has been found that about 45 to 60 minutes is adequate for the treatment of 5000 pounds of molten metal with 500 pounds of slag in an open are electric furnace of the tilting type widely used for making steel.
In extensive tests of the method of the invention, numerous batches of alloy containing 40 about to silicon and 0.17% to 2% carbon were treated as just described. In each case the carbon content of the product was no greater than 0.03%, in most instances it was substantially less than 0.03%, and in a few instances it was less 5 than 0.01%.
Although the treatment of alloy containing about 45% to 50% silicon has been emphasized herein, this is only an illustrative and preferred molten mass of said alloy or silicide in contact with a slag until practically all of said silicon carbide has entered said slag.
2. Method of treating metallic silicide, or alloy comprising a. large proportion of silicon, contain- 7 ing a small but substantial proportion of carbon as silicon carbide which comprises heating a shal- JOSEPH H. BRENNAN.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US252070A US2207282A (en) | 1939-01-21 | 1939-01-21 | Method of treating alloys |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US252070A US2207282A (en) | 1939-01-21 | 1939-01-21 | Method of treating alloys |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2207282A true US2207282A (en) | 1940-07-09 |
Family
ID=22954467
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US252070A Expired - Lifetime US2207282A (en) | 1939-01-21 | 1939-01-21 | Method of treating alloys |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2207282A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NO20180441A1 (en) * | 2018-04-03 | 2019-07-22 | Elkem Materials | Silicon based alloy, method for the production thereof and use of such alloy |
-
1939
- 1939-01-21 US US252070A patent/US2207282A/en not_active Expired - Lifetime
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NO20180441A1 (en) * | 2018-04-03 | 2019-07-22 | Elkem Materials | Silicon based alloy, method for the production thereof and use of such alloy |
| NO343946B1 (en) * | 2018-04-03 | 2019-07-22 | Elkem Materials | Silicon based alloy, method for the production thereof and use of such alloy |
| US12291764B2 (en) | 2018-04-03 | 2025-05-06 | Elkem Asa | Silicon based alloy, method for the production thereof and use of such alloy |
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