US3068094A - Alloy of iron, aluminum, and chromium - Google Patents
Alloy of iron, aluminum, and chromium Download PDFInfo
- Publication number
- US3068094A US3068094A US789240A US78924059A US3068094A US 3068094 A US3068094 A US 3068094A US 789240 A US789240 A US 789240A US 78924059 A US78924059 A US 78924059A US 3068094 A US3068094 A US 3068094A
- Authority
- US
- United States
- Prior art keywords
- aluminum
- alloy
- chromium
- percent
- iron
- 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
- 229910052782 aluminium Inorganic materials 0.000 title claims description 37
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 title claims description 37
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 title claims description 25
- 239000011651 chromium Substances 0.000 title claims description 25
- 229910052804 chromium Inorganic materials 0.000 title claims description 21
- 229910000640 Fe alloy Inorganic materials 0.000 title claims description 7
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 27
- 229910045601 alloy Inorganic materials 0.000 claims description 26
- 239000000956 alloy Substances 0.000 claims description 26
- 229910052742 iron Inorganic materials 0.000 claims description 12
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 11
- 239000001301 oxygen Substances 0.000 claims description 11
- 229910052760 oxygen Inorganic materials 0.000 claims description 11
- 238000002844 melting Methods 0.000 claims description 10
- 230000008018 melting Effects 0.000 claims description 10
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims description 9
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 9
- 229910052791 calcium Inorganic materials 0.000 claims description 9
- 239000011575 calcium Substances 0.000 claims description 9
- 230000003647 oxidation Effects 0.000 claims description 9
- 238000007254 oxidation reaction Methods 0.000 claims description 9
- 229910052799 carbon Inorganic materials 0.000 claims description 8
- 229910000599 Cr alloy Inorganic materials 0.000 claims description 5
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 3
- 239000005864 Sulphur Substances 0.000 claims description 3
- 238000011109 contamination Methods 0.000 claims description 3
- 229910052751 metal Inorganic materials 0.000 description 9
- 239000002184 metal Substances 0.000 description 9
- UPHIPHFJVNKLMR-UHFFFAOYSA-N chromium iron Chemical compound [Cr].[Fe] UPHIPHFJVNKLMR-UHFFFAOYSA-N 0.000 description 6
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 5
- 239000000155 melt Substances 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- 239000003921 oil Substances 0.000 description 5
- 229910052710 silicon Inorganic materials 0.000 description 5
- 239000010703 silicon Substances 0.000 description 5
- 239000002893 slag Substances 0.000 description 5
- 238000007792 addition Methods 0.000 description 4
- 150000002739 metals Chemical class 0.000 description 4
- 229910000604 Ferrochrome Inorganic materials 0.000 description 3
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 239000000460 chlorine Substances 0.000 description 3
- 239000010436 fluorite Substances 0.000 description 3
- 229910052719 titanium Inorganic materials 0.000 description 3
- 239000010936 titanium Substances 0.000 description 3
- 229910001018 Cast iron Inorganic materials 0.000 description 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 2
- CPLXHLVBOLITMK-UHFFFAOYSA-N Magnesium oxide Chemical compound [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 2
- 229910052801 chlorine Inorganic materials 0.000 description 2
- 238000005260 corrosion Methods 0.000 description 2
- 230000007797 corrosion Effects 0.000 description 2
- 230000006378 damage Effects 0.000 description 2
- 239000012535 impurity Substances 0.000 description 2
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- IRPGOXJVTQTAAN-UHFFFAOYSA-N 2,2,3,3,3-pentafluoropropanal Chemical compound FC(F)(F)C(F)(F)C=O IRPGOXJVTQTAAN-UHFFFAOYSA-N 0.000 description 1
- -1 ALTJMINUM Inorganic materials 0.000 description 1
- 229910000838 Al alloy Inorganic materials 0.000 description 1
- KLZUFWVZNOTSEM-UHFFFAOYSA-K Aluminum fluoride Inorganic materials F[Al](F)F KLZUFWVZNOTSEM-UHFFFAOYSA-K 0.000 description 1
- 229910000882 Ca alloy Inorganic materials 0.000 description 1
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 1
- 229910001021 Ferroalloy Inorganic materials 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 description 1
- 235000011941 Tilia x europaea Nutrition 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- KCZFLPPCFOHPNI-UHFFFAOYSA-N alumane;iron Chemical compound [AlH3].[Fe] KCZFLPPCFOHPNI-UHFFFAOYSA-N 0.000 description 1
- QQHSIRTYSFLSRM-UHFFFAOYSA-N alumanylidynechromium Chemical compound [Al].[Cr] QQHSIRTYSFLSRM-UHFFFAOYSA-N 0.000 description 1
- RGKMZNDDOBAZGW-UHFFFAOYSA-N aluminum calcium Chemical compound [Al].[Ca] RGKMZNDDOBAZGW-UHFFFAOYSA-N 0.000 description 1
- 238000005660 chlorination reaction Methods 0.000 description 1
- 239000000788 chromium alloy Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 239000010439 graphite Substances 0.000 description 1
- 229910002804 graphite Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 230000006698 induction Effects 0.000 description 1
- 239000004571 lime Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 239000000395 magnesium oxide Substances 0.000 description 1
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 238000010907 mechanical stirring Methods 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 229910052750 molybdenum Inorganic materials 0.000 description 1
- 239000011733 molybdenum Substances 0.000 description 1
- 229910052758 niobium Inorganic materials 0.000 description 1
- 239000010955 niobium Substances 0.000 description 1
- GUCVJGMIXFAOAE-UHFFFAOYSA-N niobium atom Chemical compound [Nb] GUCVJGMIXFAOAE-UHFFFAOYSA-N 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical class O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000010926 purge Methods 0.000 description 1
- 238000007711 solidification Methods 0.000 description 1
- 230000008023 solidification Effects 0.000 description 1
- 238000009628 steelmaking Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 238000004227 thermal cracking Methods 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 229910052720 vanadium Inorganic materials 0.000 description 1
- LEONUFNNVUYDNQ-UHFFFAOYSA-N vanadium atom Chemical compound [V] LEONUFNNVUYDNQ-UHFFFAOYSA-N 0.000 description 1
- 239000010455 vermiculite Substances 0.000 description 1
- 229910052902 vermiculite Inorganic materials 0.000 description 1
- 235000019354 vermiculite Nutrition 0.000 description 1
- 229910000859 α-Fe 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
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/18—Ferrous alloys, e.g. steel alloys containing chromium
Definitions
- Alloys of iron, chromium and aluminum containing 6.5 to 8.0-percent aluminum and 7.0 to 8.0 percent chromium have been found to possess remarkable resistance to carburization, sulphurization, corrosion and very high temperature oxidation combined wtih reasonable ductility provided they are prepared in a manner which assures a rigidly deoxidized and degasified product. Vacuum melting procedures may be employed to this end, but commercial considerations require that such an alloy be pre pared by an air melting technique. The exact procedure by which this rigid deoxidation is finally consummated is immaterial provided there is eventually produced a molten iron, aluminum chromium alloy containing a very low percentage of oxygen and this molten alloy is poured in a manner to retain this low oxygen content.
- electrolytic iron and ferro chromium are melted in a rammed magnesia crucible without the benefit of any slag covering. While not so limited, it is preferred that this melting be accomplished by use of high frequency currents. While the electrolytic iron and ferro chromium are being melted, a bath of molten aluminum is prepared in an ordinary teapot graphite crucible. This aluminum is held at a temperature of about 1800 F.
- a preliminary deoxidation is effected by the addition of 0.1% aluminum and 0.5% manganese, both being added as pure metals or as ferroalloys.
- a more drastic deoxidation of the molten iron chromium bath is now required. This is accomplished by exposing the melt to metallic calcium. This may best be done by wiring small cubes of metallic calcium to an iron rod and thrusting the iron rod into the melt. Calcium is preferred but for this purpose it may be replaced by an aluminum calcium alloy or by magnesium or any suitable combination of these elements. The violent ebullition of gas from the deoxidizing metal serves to purge and violently agitate the bath.
- a total of 0.5 of calcium is added to the molten iron chromium bath in two stages.
- the second of the two stages is carried out just before the mixing of the iron chromium bath and aluminum so that a slight excess of calcium remains in the melt.
- the aluminum is now deoxidized using approximately 0.1% calcium, based upon the amount of the aluminum.
- This deoxidized aluminum is then further degassed by introducing chlorine into the melt through a refractory tube. This chlorination serves to eliminate any hydrogen which may have been generated by the reaction of the aluminum and the water vapor of the air.
- the reaction of the chlorine with the aluminum bath is exothermic and tends to raise the temperature of the bath.
- fluorspar is added to the iron chromium bath after which the aluminum is slowly poured through the fluorspar slag into the iron chromium bath. All fluorspar used in this process should be rigidly anhydrous to avoid reaction between the aluminum and Water vapor.
- Cast iron molds which have been given a wash of a chlorinated pitch or exposed to a carbon tetrachloride atmosphere are used to receive this metal. It is essential that the alloy be poured into the mold promptly to prevent harmful oxidation in the crucible. The metal is poured into these Washed cast iron molds at about 2900 F. The hot topping procedure must take into account the very deep piping encountered in this type of alloy.
- the ingots are stripped from the molds and buried in a heat-insulating medium such as vermiculite or lime. This is necessary to prevent thermal cracking because of the poor thermal conductivity and high thermal coefiicient of expansion of iron aluminum alloys.
- An alloy typifying this invention has been prepared containing 7.5 percent aluminum, 7.5 percent chromium, 0.026 percent carbon, remainder iron and incidental impurities. In the oil quenched condition this alloy exhibited a tensile strength of 77,700 pounds per square inch, a yield strength of 60,400 pounds per square inch, an elongation of 35 percent and a reduction of area of 74 percent. The corresponding figures for the furnace cooled condition are 79,800 pounds per square inch, 59,- 600 pounds per square inch, 26 percent and 58 percent.
- the strength of the ferrite matrix in this alloy may be further strengthened by the addition of small amounts of metals which are strong carbide formers.
- metals which are strong carbide formers. Examples of such metals are molybdenum, titanium, niobium, and vanadium. These carbide formers should be added with caution because of their catastrophic effect upon ductility, particularly in the furnace cooled condition.
- An alloy comprising 7.90 percent aluminum, 6.75 percent chromium, 0.57 percent titanium, 0.02 percent carbon and 0.35 percent silicon exhibited an elongation in the oil quenched condition of 27 percent and in the furnace cooled condition of only 2 percent.
- a similar alloy containing 7.5 percent aluminum, 7.90 percent chromium, 1.07 percent titanium, 0.03 percent carbon and 0.35 percent silicon exhibited an elongation in the oil quenched condition of 20 percent and in the furnace cooled condition only 1 percent.
- iron when employed in the at- 3) tached claims it is to be understood to comprehend also iron alloyed with minor amounts of silicon, the carbide forming metals and impurities of an incidental nature.
- a sulphur and carbon resistant ductile and Workable alloy of iron, chromium and aluminum consisting essentially of 6.5 to 8.0 percent aluminum, 7.0 to 8.0 percent chromium, a small but significant residue of a metal having an afiinity for oxygen at the melting point of the alloy much stronger than that of aluminum and chromium, the remainder essentially iron, said alloy being free from contamination by oxides of aluminum and chromium and having an oxygen content no higher than that which corresponds to the equilibrium between calcium and oxygen at the melting point of the alloy, the oxidation resistance of this alloy being such that it is substantially unaffected by exposure to air at 2200 F. for a period of 500 hours.
- a sulphur and carbon resistant ductile and workable alloy of iron, chromium and aluminum consisting essentially of 7.5 percent aluminum, 7.5 percent chromium, a small but significant residue of a metal having an affinity for oxygen at the melting point of the alloy much stronger than that of aluminum and chromium, the remainder essentially iron, said alloy being free from contamination by oxides of aluminum and chromium and having an oxygen content no higher than that which corresponds to the equilibrium between calcium and oxygen at the melting point of the alloy, the oxidation resistance of this alloy being such that it is substantially unafiected by exposure to air at 2200" F. for a period of 500 hours.
Landscapes
- 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)
- Manufacture And Refinement Of Metals (AREA)
- Electrolytic Production Of Metals (AREA)
Description
United States Patent OfiFice 3,068,094 Patented Dec. 11, 1%62 3 068,094 ALLOY OF IRON, ALTJMINUM, AND CHROMIUM Victor F. Zackay, Dearborn, and Richard E. Heimerdinger, Detroit, Mich., assignors to The Ford Motor Company, Dearborn, Mich., a corporation of Delaware No Drawing. Filed Jan. 27, 1959, Ser. No. 789,240 2 Claims. (Cl. 75-124) This invention is concerned with the field of siderurgy and is more particularly concerned with an alloy of iron, aluminum and chromium which exhibits remarkable resistance to carburization, sulphurization, corrosion and very high temperature oxidation and concomitantly retains a high degree of ductility and workability. The alloys described herein constitute an improvement on the alloys described and claimed in United States Letters Patent 2,804,387, granted August 27, 1957, to Morgan and Zackay.
Alloys of iron, chromium and aluminum containing 6.5 to 8.0-percent aluminum and 7.0 to 8.0 percent chromium have been found to possess remarkable resistance to carburization, sulphurization, corrosion and very high temperature oxidation combined wtih reasonable ductility provided they are prepared in a manner which assures a rigidly deoxidized and degasified product. Vacuum melting procedures may be employed to this end, but commercial considerations require that such an alloy be pre pared by an air melting technique. The exact procedure by which this rigid deoxidation is finally consummated is immaterial provided there is eventually produced a molten iron, aluminum chromium alloy containing a very low percentage of oxygen and this molten alloy is poured in a manner to retain this low oxygen content.
In the preparation of this alloy, electrolytic iron and ferro chromium are melted in a rammed magnesia crucible without the benefit of any slag covering. While not so limited, it is preferred that this melting be accomplished by use of high frequency currents. While the electrolytic iron and ferro chromium are being melted, a bath of molten aluminum is prepared in an ordinary teapot graphite crucible. This aluminum is held at a temperature of about 1800 F.
After melting of the electrolytic iron and ferro chromium is complete, a preliminary deoxidation is effected by the addition of 0.1% aluminum and 0.5% manganese, both being added as pure metals or as ferroalloys. A more drastic deoxidation of the molten iron chromium bath is now required. This is accomplished by exposing the melt to metallic calcium. This may best be done by wiring small cubes of metallic calcium to an iron rod and thrusting the iron rod into the melt. Calcium is preferred but for this purpose it may be replaced by an aluminum calcium alloy or by magnesium or any suitable combination of these elements. The violent ebullition of gas from the deoxidizing metal serves to purge and violently agitate the bath. By way of example, a total of 0.5 of calcium is added to the molten iron chromium bath in two stages. The second of the two stages is carried out just before the mixing of the iron chromium bath and aluminum so that a slight excess of calcium remains in the melt.
In a manner similar to that described for the iron chromium bath the aluminum is now deoxidized using approximately 0.1% calcium, based upon the amount of the aluminum. This deoxidized aluminum is then further degassed by introducing chlorine into the melt through a refractory tube. This chlorination serves to eliminate any hydrogen which may have been generated by the reaction of the aluminum and the water vapor of the air. The reaction of the chlorine with the aluminum bath is exothermic and tends to raise the temperature of the bath. After the aluminum is completely degassed the oxidized dross is skimmed off, fluorspar is added to the iron chromium bath after which the aluminum is slowly poured through the fluorspar slag into the iron chromium bath. All fluorspar used in this process should be rigidly anhydrous to avoid reaction between the aluminum and Water vapor.
Some oxidation of the aluminum during the pouring operation is inevitable. However, this aluminum oxide reacts with the fiuorspar slag again exothermically and tends to heat the bath. Precautions should be taken to avoid any toxic effects from the aluminum fluoride which is generated at this point. It is important during and after the addition of the molten aluminum that the bath be vigorously agitated. Induction stirring per se has not been found adequate for this purpose and resort has been had to vigorous mechanical stirring.
One minute prior to pouring the agitation is stopped and the power shut off. This permits the molten slag to stratify so that the bulk of the slag can be removed. Cast iron molds which have been given a wash of a chlorinated pitch or exposed to a carbon tetrachloride atmosphere are used to receive this metal. It is essential that the alloy be poured into the mold promptly to prevent harmful oxidation in the crucible. The metal is poured into these Washed cast iron molds at about 2900 F. The hot topping procedure must take into account the very deep piping encountered in this type of alloy.
Promptly upon solidification the ingots are stripped from the molds and buried in a heat-insulating medium such as vermiculite or lime. This is necessary to prevent thermal cracking because of the poor thermal conductivity and high thermal coefiicient of expansion of iron aluminum alloys.
An alloy typifying this invention has been prepared containing 7.5 percent aluminum, 7.5 percent chromium, 0.026 percent carbon, remainder iron and incidental impurities. In the oil quenched condition this alloy exhibited a tensile strength of 77,700 pounds per square inch, a yield strength of 60,400 pounds per square inch, an elongation of 35 percent and a reduction of area of 74 percent. The corresponding figures for the furnace cooled condition are 79,800 pounds per square inch, 59,- 600 pounds per square inch, 26 percent and 58 percent.
In commercial practice it is diflicult to exclude silicon from the melts. Furthermore, this element tends to enhance the resistance of the alloy to oxidation and carburization. This additional resistance to oxidation and carburization is obtained only at a heavy sacrifice of ductility as expressed in the elongation value. An alloy containing 7.71 percent aluminum, 7.54 percent chromium, 0.05 percent carbon, 0.34 percent silicon, remainder substantially all iron exhibited an elongation of 17 percent in the oil quenched condition and 12 percent in the furnace cooled condition.
The strength of the ferrite matrix in this alloy may be further strengthened by the addition of small amounts of metals which are strong carbide formers. Examples of such metals are molybdenum, titanium, niobium, and vanadium. These carbide formers should be added with caution because of their catastrophic effect upon ductility, particularly in the furnace cooled condition. An alloy comprising 7.90 percent aluminum, 6.75 percent chromium, 0.57 percent titanium, 0.02 percent carbon and 0.35 percent silicon exhibited an elongation in the oil quenched condition of 27 percent and in the furnace cooled condition of only 2 percent. A similar alloy containing 7.5 percent aluminum, 7.90 percent chromium, 1.07 percent titanium, 0.03 percent carbon and 0.35 percent silicon exhibited an elongation in the oil quenched condition of 20 percent and in the furnace cooled condition only 1 percent.
Accordingly, when the term iron is employed in the at- 3) tached claims it is to be understood to comprehend also iron alloyed with minor amounts of silicon, the carbide forming metals and impurities of an incidental nature.
The critical nature of the aluminum additions is shown from the fact that an alloy comprising 8.28 percent aluminurn, 6.93 percent chromium, 0.03 percent carbon and balance substantially all iron exhibited in the oil quenched condition an elongation and reduction of area of 15 percent and in the furnace cooled condition of 21 and 27 percent, respectively. To resist even one hundred hours exposure to air at 2000 F. a minimum aluminum content of 6 percent is necessary. No numerical data is available to support this statement, but it may be clearly demonstrated in colored photographs which are not included because of the difiiculties in reproducing colored photographs. Similarly it can be demonstrated by means of colored photographs that alloys containing 8.0 percent aluminum and up to 4.75 percent chromium, balance substantially all iron are heavily damaged by exposure to air at 2200 F. for 500 hours. The same test does no substantial harm to a specimen containing 7.25 percent chromium, and heavily damages one containing 9.50 percent chromium.
We claim as our invention:
1. A sulphur and carbon resistant ductile and Workable alloy of iron, chromium and aluminum consisting essentially of 6.5 to 8.0 percent aluminum, 7.0 to 8.0 percent chromium, a small but significant residue of a metal having an afiinity for oxygen at the melting point of the alloy much stronger than that of aluminum and chromium, the remainder essentially iron, said alloy being free from contamination by oxides of aluminum and chromium and having an oxygen content no higher than that which corresponds to the equilibrium between calcium and oxygen at the melting point of the alloy, the oxidation resistance of this alloy being such that it is substantially unaffected by exposure to air at 2200 F. for a period of 500 hours.
2. A sulphur and carbon resistant ductile and workable alloy of iron, chromium and aluminum consisting essentially of 7.5 percent aluminum, 7.5 percent chromium, a small but significant residue of a metal having an affinity for oxygen at the melting point of the alloy much stronger than that of aluminum and chromium, the remainder essentially iron, said alloy being free from contamination by oxides of aluminum and chromium and having an oxygen content no higher than that which corresponds to the equilibrium between calcium and oxygen at the melting point of the alloy, the oxidation resistance of this alloy being such that it is substantially unafiected by exposure to air at 2200" F. for a period of 500 hours.
References Cited in the file of this patent UNITED STATES PATENTS 2,703,355 Hagglund Mar. 1, 1955 2,804,387 Morgan et a1 Aug. 27, 1957 2,941,883 Ida et al June 21, 1960 2,987,394 Mueller et al. June 6, 1961 OTHER REFERENCES Basic Open Hearth Steelmaking," 1944, page 499. Published by the American Institute of Mining and Metallurgical Engineers.
Claims (1)
1. A SULPHUR AND CARBON RESISTANT DUCTILE AND WORKABLE ALLOY OF IRON, CHROMIUM AND ALUMINUM CONSISTING ESSENTIALLY OF 6.5 TO 8.0 PERCENT ALUMINUM, 7.0 TO 8.0 PERCENT CHROMIUM, A SMALL BUT SIGNIFICANT RESIDUE OF A METAL HAVING AN AFFINITY FOR OXYGEN AT THE MELTING POINT OF THE ALLOY MUCH STRONGER THAN THAT OF ALUMINUM AND CHROMIUM, THE REMAINDER ESSENTIALLY IRON, SAID ALLOY BEING FREE FROM CONTAMINATION BY OXIDES OF ALUMINUM AND CHROMIUM AND HAVING AN OXYGEN CONTENT NO HIGHER THAN THAT WHICH CORREPONDS TO THE EQUILIBRIUM BETWEEN CALCIUM AND OXYGEN AT THE MELTING POINT OF THE ALLOY, THE OXIDATION RESISTANCE OF THIS ALLOY BEING SUCH THAT IT IS SUBSTANTIALLY UNAFFECTED BY EXPOSURE TO AIR AT 2200*F. FOR A PERIOD OF 500 HOURS.
Priority Applications (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US789240A US3068094A (en) | 1959-01-27 | 1959-01-27 | Alloy of iron, aluminum, and chromium |
| GB2914/60A GB944124A (en) | 1959-01-27 | 1960-01-27 | Iron-chromium-aluminium alloy |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US789240A US3068094A (en) | 1959-01-27 | 1959-01-27 | Alloy of iron, aluminum, and chromium |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US3068094A true US3068094A (en) | 1962-12-11 |
Family
ID=25147019
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US789240A Expired - Lifetime US3068094A (en) | 1959-01-27 | 1959-01-27 | Alloy of iron, aluminum, and chromium |
Country Status (2)
| Country | Link |
|---|---|
| US (1) | US3068094A (en) |
| GB (1) | GB944124A (en) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3660173A (en) * | 1969-06-25 | 1972-05-02 | Toyo Kogyo Co | Method of preparing corrosion resistant metallic articles |
| US3859079A (en) * | 1972-08-09 | 1975-01-07 | Bethlehem Steel Corp | High temperature oxidation resistant alloy |
| US3893849A (en) * | 1970-10-30 | 1975-07-08 | United States Steel Corp | Oxidation-resistant ferritic stainless steel |
| US4316743A (en) * | 1973-10-29 | 1982-02-23 | Tokyo Shibaura Electric Co., Ltd. | High damping Fe-Cr-Al alloy |
Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2703355A (en) * | 1950-10-23 | 1955-03-01 | Kanthal Corp | Electric heater |
| US2804387A (en) * | 1955-11-14 | 1957-08-27 | Ford Motor Co | Preparation of iron aluminum alloys |
| US2941883A (en) * | 1957-10-02 | 1960-06-21 | Martin Co | Alloy especially suited to cladding nuclear fuel elements |
| US2987394A (en) * | 1959-03-25 | 1961-06-06 | John J Mueller | Iron-aluminum base alloys |
-
1959
- 1959-01-27 US US789240A patent/US3068094A/en not_active Expired - Lifetime
-
1960
- 1960-01-27 GB GB2914/60A patent/GB944124A/en not_active Expired
Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2703355A (en) * | 1950-10-23 | 1955-03-01 | Kanthal Corp | Electric heater |
| US2804387A (en) * | 1955-11-14 | 1957-08-27 | Ford Motor Co | Preparation of iron aluminum alloys |
| US2941883A (en) * | 1957-10-02 | 1960-06-21 | Martin Co | Alloy especially suited to cladding nuclear fuel elements |
| US2987394A (en) * | 1959-03-25 | 1961-06-06 | John J Mueller | Iron-aluminum base alloys |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3660173A (en) * | 1969-06-25 | 1972-05-02 | Toyo Kogyo Co | Method of preparing corrosion resistant metallic articles |
| US3893849A (en) * | 1970-10-30 | 1975-07-08 | United States Steel Corp | Oxidation-resistant ferritic stainless steel |
| US3859079A (en) * | 1972-08-09 | 1975-01-07 | Bethlehem Steel Corp | High temperature oxidation resistant alloy |
| US4316743A (en) * | 1973-10-29 | 1982-02-23 | Tokyo Shibaura Electric Co., Ltd. | High damping Fe-Cr-Al alloy |
Also Published As
| Publication number | Publication date |
|---|---|
| GB944124A (en) | 1963-12-11 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US3068094A (en) | Alloy of iron, aluminum, and chromium | |
| US3759758A (en) | High strength aluminum casting alloy | |
| JP2002161308A (en) | Method of manufacturing high strength, high fatigue resistance structural steel | |
| US3615348A (en) | Stainless steel melting practice | |
| US2683662A (en) | Manufacture of iron and steel and products obtained | |
| US3172758A (en) | Oxygen process for producing high | |
| CN110923569B (en) | Large-section stainless steel forged tube with nuclear grade high strength and high intergranular corrosion resistance and its manufacturing method | |
| US2804387A (en) | Preparation of iron aluminum alloys | |
| US2238160A (en) | Method of making nickel-chromium alloys | |
| US2693414A (en) | Methods of casting titanium stabilized steel | |
| US2990272A (en) | Desulphurizing molten iron | |
| US490961A (en) | Process of producing metallic alloys | |
| US935863A (en) | Alloy and process for its production. | |
| US1415733A (en) | Process of making and using metal scavenging alloy | |
| US501233A (en) | Alloy | |
| US1544037A (en) | Nickel-chromium alloy and process of making same | |
| US1365091A (en) | Allot | |
| US1811696A (en) | Carbon-free metal | |
| CN110629105A (en) | A kind of ceramic quenched and tempered steel and preparation method thereof | |
| US2467701A (en) | Heat-resistant low alloy steels | |
| US2064441A (en) | Process of making manganese chromium steel | |
| US1970067A (en) | Process for the production of ageresisting iron and steel | |
| US1508211A (en) | Process of making rustless iron and similar alloys | |
| SU1705395A1 (en) | Cast iron | |
| USRE19725E (en) | Carbon-free metal |