US2336237A - Alloy process - Google Patents
Alloy process Download PDFInfo
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- US2336237A US2336237A US396913A US39691341A US2336237A US 2336237 A US2336237 A US 2336237A US 396913 A US396913 A US 396913A US 39691341 A US39691341 A US 39691341A US 2336237 A US2336237 A US 2336237A
- Authority
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- United States
- Prior art keywords
- columbium
- bath
- metal
- ore
- chromium
- 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
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- 238000000034 method Methods 0.000 title description 20
- 230000008569 process Effects 0.000 title description 15
- 229910045601 alloy Inorganic materials 0.000 title description 5
- 239000000956 alloy Substances 0.000 title description 5
- 239000010955 niobium Substances 0.000 description 36
- GUCVJGMIXFAOAE-UHFFFAOYSA-N niobium atom Chemical compound [Nb] GUCVJGMIXFAOAE-UHFFFAOYSA-N 0.000 description 36
- 229910052751 metal Inorganic materials 0.000 description 28
- 239000002184 metal Substances 0.000 description 28
- 229910001220 stainless steel Inorganic materials 0.000 description 21
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 18
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 15
- 229910000831 Steel Inorganic materials 0.000 description 15
- 239000010959 steel Substances 0.000 description 15
- 229910052799 carbon Inorganic materials 0.000 description 14
- 229910052804 chromium Inorganic materials 0.000 description 14
- 239000011651 chromium Substances 0.000 description 14
- 238000005260 corrosion Methods 0.000 description 13
- 230000007797 corrosion Effects 0.000 description 13
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 12
- 229910052710 silicon Inorganic materials 0.000 description 12
- 239000010703 silicon Substances 0.000 description 12
- 239000002893 slag Substances 0.000 description 12
- 239000010935 stainless steel Substances 0.000 description 12
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 10
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 10
- 238000004519 manufacturing process Methods 0.000 description 10
- 229910052759 nickel Inorganic materials 0.000 description 9
- 239000003638 chemical reducing agent Substances 0.000 description 8
- 239000000203 mixture Substances 0.000 description 7
- 229910052742 iron Inorganic materials 0.000 description 6
- 239000000047 product Substances 0.000 description 5
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 4
- 235000011941 Tilia x europaea Nutrition 0.000 description 4
- 238000007792 addition Methods 0.000 description 4
- 229910052782 aluminium Inorganic materials 0.000 description 4
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 4
- 239000004571 lime Substances 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 230000009467 reduction Effects 0.000 description 4
- 238000006722 reduction reaction Methods 0.000 description 4
- CWYNVVGOOAEACU-UHFFFAOYSA-N Fe2+ Chemical compound [Fe+2] CWYNVVGOOAEACU-UHFFFAOYSA-N 0.000 description 3
- 229910000519 Ferrosilicon Inorganic materials 0.000 description 3
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 3
- 238000005275 alloying Methods 0.000 description 3
- 238000002844 melting Methods 0.000 description 3
- 230000008018 melting Effects 0.000 description 3
- 150000002739 metals Chemical class 0.000 description 3
- 239000002245 particle Substances 0.000 description 3
- 229910001256 stainless steel alloy Inorganic materials 0.000 description 3
- 230000000153 supplemental effect Effects 0.000 description 3
- 239000010936 titanium Substances 0.000 description 3
- 229910052719 titanium Inorganic materials 0.000 description 3
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 2
- 229910000604 Ferrochrome Inorganic materials 0.000 description 2
- 229910000592 Ferroniobium Inorganic materials 0.000 description 2
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 description 2
- BUGBHKTXTAQXES-UHFFFAOYSA-N Selenium Chemical compound [Se] BUGBHKTXTAQXES-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 2
- 239000005864 Sulphur Substances 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 229910052791 calcium Inorganic materials 0.000 description 2
- 239000011575 calcium Substances 0.000 description 2
- OSMSIOKMMFKNIL-UHFFFAOYSA-N calcium;silicon Chemical compound [Ca]=[Si] OSMSIOKMMFKNIL-UHFFFAOYSA-N 0.000 description 2
- 230000008859 change Effects 0.000 description 2
- UFGZSIPAQKLCGR-UHFFFAOYSA-N chromium carbide Chemical compound [Cr]#C[Cr]C#[Cr] UFGZSIPAQKLCGR-UHFFFAOYSA-N 0.000 description 2
- 229910052802 copper Inorganic materials 0.000 description 2
- 239000010949 copper Substances 0.000 description 2
- BHEPBYXIRTUNPN-UHFFFAOYSA-N hydridophosphorus(.) (triplet) Chemical compound [PH] BHEPBYXIRTUNPN-UHFFFAOYSA-N 0.000 description 2
- 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 2
- 229910052750 molybdenum Inorganic materials 0.000 description 2
- 239000011733 molybdenum Substances 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- 230000001590 oxidative effect Effects 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- 239000011669 selenium Substances 0.000 description 2
- 229910052711 selenium Inorganic materials 0.000 description 2
- 229910052714 tellurium Inorganic materials 0.000 description 2
- PORWMNRCUJJQNO-UHFFFAOYSA-N tellurium atom Chemical compound [Te] PORWMNRCUJJQNO-UHFFFAOYSA-N 0.000 description 2
- 229910003470 tongbaite Inorganic materials 0.000 description 2
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 description 2
- 229910052721 tungsten Inorganic materials 0.000 description 2
- 239000010937 tungsten Substances 0.000 description 2
- 229910052720 vanadium Inorganic materials 0.000 description 2
- LEONUFNNVUYDNQ-UHFFFAOYSA-N vanadium atom Chemical compound [V] LEONUFNNVUYDNQ-UHFFFAOYSA-N 0.000 description 2
- 229910001209 Low-carbon steel Inorganic materials 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 229910002065 alloy metal Inorganic materials 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- VNNRSPGTAMTISX-UHFFFAOYSA-N chromium nickel Chemical compound [Cr].[Ni] VNNRSPGTAMTISX-UHFFFAOYSA-N 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 150000001247 metal acetylides Chemical class 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000006104 solid solution Substances 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 238000003466 welding Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/18—Ferrous alloys, e.g. steel alloys containing chromium
- C22C38/40—Ferrous alloys, e.g. steel alloys containing chromium with nickel
- C22C38/48—Ferrous alloys, e.g. steel alloys containing chromium with nickel with niobium or tantalum
Definitions
- This invention relates to stainless steels and more particularly to an art of producing the same.
- the invention accordingly consists in the combination of elements, composition of ingredients, and in the several steps and the relation of each of the same to one or more of the others as described herein, the scope .of the application of which is indicated in the following claims.
- stainless steel is defined as a low-carbon steel comprising to 35% chromium, with or without nickel and supplemental additions of such elements as manganese, silicon, copper, tungsten, vanadium, molybdenum, titanium, columbium, sulphur, phosphorous, selenium, tellurium, and the like for special purposes, and the balance substantially all iron.
- austenitic steels are defined as steel comprising 7% to nickel, 10 %to chromium, with or without the supplemental additions noted for special purposes, and the balance substantially all iron.
- the austenitic stainles steels are not found to be especially adapted for duty under strongly oxidizing or corrosive conditions, or conditions involving appreciable working stresses following a heating within a certain critical temperature range of some 500-900 C., largely'because of the susceptibility of thesesteels t'o intergranular corrosion. Moreover, while these steels are welded throughout the alloy with theresults that little quite readily, much difflculty is encountered in that intergranular corrosion develops adjacent to the welded sections of the metal.
- an object of my invention is to provide a practical process for introducing columbium into stainless steels by the direct use of columbium-containing ore, which process is adapted for practice during th finishing stages undergone by the metal bath, which enables a high percentage of columbium in the ore to ex-' change from the ore to the metal bath, which is practiced without encountering excessive amounts of slag, and which permits the production of a finished alloy having high corrosion resistance; particularly with respect to intergranular co" rosion.
- columbium ore preferably is crushed, and then it is mixed with a certain quantity of metallic reducing material such as calcium, calcium-silicon, silicon, aluminum, ferrosilicon, or ferroaluminum. The mixture of crushed ore and reducing material is changed into a bath of stainless steel.
- the bath of stainless steel of desired analysis is first prepared and any slag is removed. Then a finishing slag of lime and fiuorspar is prepared on the surface of the metal.
- the resultant ingots are converted through known methods into plate, sheet, strip, bars, rod, wire, tube and the like which subsequently are fabricated, as by welding, into a host of articles of ultimate use.
- the metal is tapped from the furnace into a ladle for teeming into ingot molds and where it tenitic steels in which the columbium-to-carbon ratio is approximately 10 to 1 possess high resistance to intergranular corrosion together with good workability.
- the amount of reducing agent which I mix with columbium ore is governed by the quantity thereof needed to effect reduction of the ore, Excess amounts of the reducing agent are generally used.
- the ratio of columbite ore to aluminum or silicon should be approximately 3 to 1.
- the recovery is approximately 80 percent.
- Austenitic stainless steels finished in accordance with my invention usually comprise 7% to 15% nickel, 10% to 35% chromium, 0.03% to 0.12% carbon, 0.3% to 1.2% columbium, less than 1% silicon or aluminum with or without supplemental amounts of one or more of such elements as manganese, copper, tungsten, molybdenum, titanium, vanadium, sulphur, phosphorous, selenium, tellurium, and the like, for special purposes, and the balance substantially all iron.
- a finishing slag preferably is prepared on the sur face of the reduced bath by scattering lime and fiuorspar over the bath surface.
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Treatment Of Steel In Its Molten State (AREA)
Description
Patented Dec. 7, 1943 ALLOY PROCESS Alexander L. Feild, Towson, Md., assignor to Rustless Iron and Steel Corporation, a corporation of Delaware No Drawing. Application June 6, 1941, Serial No. 396,913
Claims.
This invention relates to stainless steels and more particularly to an art of producing the same.
Among the objects of my invention is the provision of'a process having great utility in the production of stainless steels containing columbium, which permits the introduction of colum bium into stainless steel in a simple, direct and economical manner, giving a lustrous, workable, corrosion-resistant product, which enables the production of stainless steel possessing high resistance to intergranular corrosion and embrittlement. 1
Other objects in part will be obvious and, in part, will be pointed out hereinafter.
The invention accordingly consists in the combination of elements, composition of ingredients, and in the several steps and the relation of each of the same to one or more of the others as described herein, the scope .of the application of which is indicated in the following claims.
As conducive to a. clearer understanding of certain aspects of my invention, it may be noted at this point that stainless steel is defined as a low-carbon steel comprising to 35% chromium, with or without nickel and supplemental additions of such elements as manganese, silicon, copper, tungsten, vanadium, molybdenum, titanium, columbium, sulphur, phosphorous, selenium, tellurium, and the like for special purposes, and the balance substantially all iron.
Among the stainless steels to' which my invention most particularly relates, are the austenitic steels. These steels are defined as steel comprising 7% to nickel, 10 %to chromium, with or without the supplemental additions noted for special purposes, and the balance substantially all iron.
The austenitic stainles steels are not found to be especially adapted for duty under strongly oxidizing or corrosive conditions, or conditions involving appreciable working stresses following a heating within a certain critical temperature range of some 500-900 C., largely'because of the susceptibility of thesesteels t'o intergranular corrosion. Moreover, while these steels are welded throughout the alloy with theresults that little quite readily, much difflculty is encountered in that intergranular corrosion develops adjacent to the welded sections of the metal.
The phenomenon of intergranular corrosion of metals has been explained by the formation and precipitation of carbides at the grain boundaries leaving the metal susceptible'to attack at these boundaries. When austenitic stainless teels are heated, carbon comes out of solid solution. Car-,-
bide particles accumulate at the metal .grain boundaries, apparently obtaining most of the chromium from the surface of the grains. Decreased amounts of chromium near the surface of the metal grain make these metal grains less resistant to corrosion. As long as carbide particles ar dispersed throughout the grains, the possibility of intergranular corrosion is negligible, but when strong chromium carbide particles precipitate to the grain boundaries, corrosion will take place and the metal often is no longer suitable for service. Moreover, intergranular corrosion causes the metal to become embrittled and weak and the utility of the metal accordingly is P impaired still further.
The problem of preventing intergranular chromium carbide formation in austenitic stainless.
steels has been dealt with by introducing certain alloying elements into the steel. For example, such metals as titanium and columbium have been used for. this purpose with good results. These metals are very strong carbide formers and they, therefore, prevent the precipitated carbon from becoming available to combine with chromium as mentioned hereinbefore. Chromium dispersion remain substantially the same or no corrosive action takes place.
Methods heretofore employed in introducing columbium into stainless steel are expensive, in-' direct or otherwise unsatisfactory. For example, a prealloy of ferro-columbium has been much used in the manufacture of columbium-containing steel, but this prealloy has certainproperties making it undesirable for use as a material to be introduced intosteel baths. Because of the high melting point of ferro-columbium, it is diflicult dissolve the prealloy in a teel bath rapidly a d without considerable oxidation of the columbium. Moreover, prealloys' of low-carbon content are costly to prepare or to procure. Introducing an alloying element into a metal bath through the medium of a prealloy is a more indirect operation than if the elements were reduced directly from its ore. v A
The need for a more simple, direct and economical process for producing columbium-containing stainless steels has been recognized for quite some time. The direct use, in the furnace, of ores comprising substantial amounts of columbium, heretofore has been given consideration. Because of poorly directed experiments, such practicewas deemed to be impractical; Columbium'yield from the. ore proved to be much too low for commercial purposes.
Accordingly. an object of my invention is to provide a practical process for introducing columbium into stainless steels by the direct use of columbium-containing ore, which process is adapted for practice during th finishing stages undergone by the metal bath, which enables a high percentage of columbium in the ore to ex-' change from the ore to the metal bath, which is practiced without encountering excessive amounts of slag, and which permits the production of a finished alloy having high corrosion resistance; particularly with respect to intergranular co" rosion.
Referring now, more particularly to the practice of my invention, I introduce columbium ore together with a suitable reducing agent into a bath of stainless steel as a part of th steel finishing operation. I find that columbite. which contains substantial amounts of columbium oxide,
is a satisfactory source of columbium. The columbium ore preferably is crushed, and then it is mixed with a certain quantity of metallic reducing material such as calcium, calcium-silicon, silicon, aluminum, ferrosilicon, or ferroaluminum. The mixture of crushed ore and reducing material is changed into a bath of stainless steel.
Ordinarily the bath of stainless steel of desired analysis is first prepared and any slag is removed. Then a finishing slag of lime and fiuorspar is prepared on the surface of the metal.
. The columbite and reducing agent are added to the finishing slag overlying the alloy metal bath. Columbium reduced from the ore goes into the bath quite readily. The gangue from the ore and the silicon or alumina resulting from the reduc tion remain in the slag. The bath of metal, now
.containing a desired amount of columbium, is
tapped into a ladle and from the ladle is teemed into a mold to solidify and cool. The resultant ingots are converted through known methods into plate, sheet, strip, bars, rod, wire, tube and the like which subsequently are fabricated, as by welding, into a host of articles of ultimate use.
As illustrative of the practice of my invention,
"I p oduce a 13-ton heat of austenitic grade of chromium-nickel stainless steel in a suitable f urnace; for example, by melting stainless steel scrap and high-carbon ferrochrome under strongly oxidizing conditions as, wherein carbon is eliminated and chromium is oxidized and the oxide migrates to the slag, and then reducing the chromic oxides in the slag as described in Patent No. 1,925,182 to Feild, issued September 5, 1933. The heat of metal also may be produced in accordanc with the method disclosed in the Arnes Patent No. 1,954,400, issued April 10, 1934, wherein similar oxidation and reduction periods are used and wherein rustless iron scrap and chromium ore are employed as principal sources of chromium;
or inaccordance with the similar method described and claimed in the'Arness Patent No. 2,056,162, issued October 6, 1936, wherein rustless iron scrap, chrome ore and high-carbon ferrochrome are used. The nickel addition is made of austenitic steel. For a 13-min heat having a carbon content of .10% and available columbite analyzing 60% CbzOs, 775 pounds of columbiteand 155 pounds of contained silicon are employed to give a columbium to carbon ratio of 10 to 1; Columbite in the bath is reduced to columbium by the silicon, the metallic columbium going into the steel and the formed silica remaining in the slag. The metal is tapped from the furnace into a ladle for teeming into ingot molds and where it tenitic steels in which the columbium-to-carbon ratio is approximately 10 to 1 possess high resistance to intergranular corrosion together with good workability.
The amount of reducing agent which I mix with columbium ore is governed by the quantity thereof needed to effect reduction of the ore, Excess amounts of the reducing agent are generally used.
I find that the ratio of columbite ore to aluminum or silicon, for example, should be approximately 3 to 1. The recovery is approximately 80 percent.
Austenitic stainless steels finished in accordance with my invention usually comprise 7% to 15% nickel, 10% to 35% chromium, 0.03% to 0.12% carbon, 0.3% to 1.2% columbium, less than 1% silicon or aluminum with or without supplemental amounts of one or more of such elements as manganese, copper, tungsten, molybdenum, titanium, vanadium, sulphur, phosphorous, selenium, tellurium, and the like, for special purposes, and the balance substantially all iron.
The materials employed in my. process are cheap and readily available. My process is adapted to form a part of conventional metal finishing operations and requires little or no altering or shifting of metallurgical equipment usually employed in the production of stainless steel. The process is direct, since raw materials are introduced directly as a part of the metal finishing procedure. I find that the stainless steels readily take up the columbium content of the columbite ore. Only small waste of raw materials, therefore, is involved in the practice of during the melting period conveniently as electrolytic nickel.
Following the reduction of the heat of metal. I remove the slag formed on the surface of the metal bath. A carbon analysis is quickly made.
A finishing slag preferably is prepared on the sur face of the reduced bath by scattering lime and fiuorspar over the bath surface.
I then introduce a mixture comprising pulverizedwolumbite and ferrosilicon into the bath my process. Fnished alloy products are obtained in a simple, inexpensive manner; these products being clean, strong, and durable."
Although the application of my process to the production of austenitic grade stainless steels has been stressed hereinbefore, it is to be understood quite clearly that the process is suitable for other applications. employed in alloying columbium with stainless steels of the ferritic grade, the only change in the steps hereinbeforenoted being that columbite ore is introduced into a bath of stainless steel of ferritic quality rather than of the austenitic grade.
I find that when ore containing an oxide of columbium is introduced in pulverized form into a bath of stainless steel, the ore yields a good amount of columbium to the bath. Metallic reducing agents such as calcium, calcium-silicon, silicon, aluminum, ferrosilicon or ferroaluminum, or combinations thereof, are added to the For example, my process may be bath-either'in admixture with thecolumbium ore or separately from the columbium ore;
Thus it will be seen that in the present inven- -tion,- a new process for introducing columbium into stainless'steels is provided, by the use of which the various objects hereinbefore noted,
, along with many thoroughly practical advantages, are successfully achieved, It will be seen that the products made in accordance with-this process are clean, strong, workable and highly resistant to corrosion, particularly to intergranular corrosion, and that these characteristics are achieved at great savings in manufacture heretofore unrealized; and that the field of application of these products has been. broadened from the standpoint of economy without sacrificing quality. v
As many possible embodiments may be made of to be understood that all matter described herein is to be interpreted as illustrative and not in a includes preparing in a suitable furnace a bath of austenitic grade fertous' lnetal comprising my invention and as many changes'may be made 'in theembodiment hereinbefore set forth, it is substantial amounts of chromium and nickel, and
introducing into the bath in the presence of a limy finishing slag a quantity of columbium oxide and a term-silicon reducing agent as a metal finishing step.
3. In the production of stainless steel alloys of appreciable columbium contents, the art which includes preparing in a suitable furnace a lowcarbon bath of ,ferrous metal containing chromium and nickel in substantially the amounts desired in the finished steel, introducing columbium into the'bath as a finishing step by addition to the bath of lime and a mixture comprising substantially three parts columbite and one part silicon-containing reducing agent, the ratio between the columbium introduced and the carbon in said bath being substantially, 10 to 1.
4. In the production of stainless steel alloys of appreciable columbium contents, the art which includes preparing in a suitable furnace a bath of austenitic grade ferrous metal comprising 10% to 35% chromium, 7% to 15% nickel, and 0.03% to 0.12% carbon, and introducing into the bath as a metal finishing step' lime and a mixture comprising substantially three parts columbite and one part silicon reducing agent.
5. In the production of stainless steel alloys of appreciable columbium contents, the art which includes preparing in a suitable furnace a bath of austenitic grade ferrous metal comprising 10% to 35% chromium, 7% to 15% nickel, and 0.03% to 0.12% carbon, preparing a limy finishing slag on the ,bath and introducing into the bath as a metal finishing step a mixture comprisingcolumbite and crushed term-silicon.
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Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US396913A US2336237A (en) | 1941-06-06 | 1941-06-06 | Alloy process |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US396913A US2336237A (en) | 1941-06-06 | 1941-06-06 | Alloy process |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2336237A true US2336237A (en) | 1943-12-07 |
Family
ID=23569099
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US396913A Expired - Lifetime US2336237A (en) | 1941-06-06 | 1941-06-06 | Alloy process |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2336237A (en) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2430671A (en) * | 1943-12-02 | 1947-11-11 | American Rolling Mill Co | Alloy process |
| US2482948A (en) * | 1946-11-11 | 1949-09-27 | Doris Wright | Method for the production of columbium containing steel |
| US2564474A (en) * | 1948-01-21 | 1951-08-14 | Armco Steel Corp | Weld rod and coating therefor |
-
1941
- 1941-06-06 US US396913A patent/US2336237A/en not_active Expired - Lifetime
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2430671A (en) * | 1943-12-02 | 1947-11-11 | American Rolling Mill Co | Alloy process |
| US2482948A (en) * | 1946-11-11 | 1949-09-27 | Doris Wright | Method for the production of columbium containing steel |
| US2564474A (en) * | 1948-01-21 | 1951-08-14 | Armco Steel Corp | Weld rod and coating therefor |
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