EP0549286A1 - High temperature resistant Ni-Cr alloy - Google Patents

High temperature resistant Ni-Cr alloy Download PDF

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Publication number
EP0549286A1
EP0549286A1 EP92311611A EP92311611A EP0549286A1 EP 0549286 A1 EP0549286 A1 EP 0549286A1 EP 92311611 A EP92311611 A EP 92311611A EP 92311611 A EP92311611 A EP 92311611A EP 0549286 A1 EP0549286 A1 EP 0549286A1
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alloy
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cerium
magnesium
yttrium
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EP0549286B1 (en
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Ian Christopher Elliott
Wai-Yan Chan
Norman Charles Farr
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Inco Alloys Ltd
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Inco Alloys Ltd
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    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C19/00Alloys based on nickel or cobalt
    • C22C19/03Alloys based on nickel or cobalt based on nickel
    • C22C19/05Alloys based on nickel or cobalt based on nickel with chromium
    • C22C19/058Alloys based on nickel or cobalt based on nickel with chromium without Mo and W

Definitions

  • This invention is related to the field of Ni-Cr-Fe alloys and particularly to alloys used in high temperature (1200°C) applications.
  • Ni-Cr-Fe alloys such as INCONEL® alloy 601 have historically been used for general-purpose engineering applications requiring heat and corrosion resistance. (INCONEL is a registered trademark of the Inco family of companies.) In addition, INCONEL alloy 601 has excellent resistance to thermal cycle fatigue in combination with high temperature oxidation resistance. Commercial uses of INCONEL alloy 601 include thermal processing equipment, chemical processing applications, petrochemical applications, pollution control applications and turbine engine components.
  • INCONEL alloy 601 has been widely used as a roller alloy for applications within high temperature kilns used in firing of ceramic tiles.
  • rollers are typically exposed to oxidizing conditions at temperatures as high as 1000°C or 1165°C. At such high temperatures, roller alloys have a tendency to slowly fail due to gradual oxidation. At increased temperatures of about 1200°C, oxidation rate and spalling rate increase unacceptably.
  • the invention provides a heat and corrosion resistant alloy having, by weight percent, 55-65% nickel, 19-25% chromium, 1-4.5% aluminum, 0.045-0.3% yttrium, 0.15-1% titanium, 0.005-0.5% carbon, 0.1-1.5% silicon, 0-1% manganese, at least 0.005% total magnesium, calcium and/or cerium, less than 0.5% total magnesium and/or calcium, less than 1% cerium, 0.0001-0.1% boron, 0-0.5% zirconium, 0.0001-0.1% nitrogen, 0-10% cobalt and balance iron and incidental impurities.
  • Figure 1 is a plot of mass change versus time for various alloys in an air atmosphere at 1165°C.
  • Figure 2 is a plot of mass charge versus time for various alloys in an air atmosphere at 1200°C.
  • the invention provides a Ni-Cr-Fe-Al alloy with improved high temperature cyclic oxidation resistance.
  • a nickel-base alloy containing a combination of chromium, yttrium, silicon and aluminum has been found to dramatically improve oxidation resistance at 1200°C.
  • the 1200°C temperature is particularly useful for kilns used for firing lead-free frits.
  • test heats of Ni-Cr-Fe alloys were cast into 10 kg ingots.
  • Ingot 7 originated from a commercial heat.
  • Chemical compositions of the test heats expressed in weight percent are given below in Table 1. (All compositions in this specification are expressed in weight percent unless specifically indicated.)
  • Ingot numbers 1-6 represent experimental heats; and Ingot number 7 represents an alloy within the commercial range of INCONEL alloy 601.
  • the ingots were machined, dressed and forged at 1140°C into 50.8 mm round bars. The round bars were annealed at 1175°C for 30 minutes.
  • Test coupons were machined from forged bar into plates having approximate dimensions of 15 mm x 20 mm x 3 mm. Plates were pierced with a 3 mm diameter hole for poaching the coupon to a jig. All oxidation test specimens were polished with silicon carbide paper to a 240 grade finish. Following recordation of sample size, all test samples were degreased and dried in hot air. The test specimens were given a cyclic oxidation test of 168 hours in a 1200°C air atmosphere furnace followed by a 20 minutes cooling cycle. Results from the cyclic oxidation test are given below in Table 2.
  • sample numbers correspond to the ingot numbers of Table 1. From the above high temperature experiment it was determined that the composition of ingot 4 at 1200°C provided the best oxidation resistance. Scale integrity was found to increase with decreased amounts of titanium. Segregation of yttrium rich phases at the alloy/scale interface was found to increase scale adhesion and may have an effect in modifying alloy oxidation mechanism leading to improved oxidation resistance. The tightly adherent scale layer of high yttrium sample number 4 was found to provide an effective barrier for preventing internal oxidation. In addition, the increased aluminum content of sample number 4 was believed to also contribute high temperature stability of the oxide scale.
  • Alloy A provided a Ni-Cr-Fe-Al alloy with improved high temperature (1200°C) oxidation resistance.
  • a combination of chromium, yttrium, silicon and aluminum was found to dramatically improve oxidation resistance.
  • the improved Ni-Cr -Fe-Al alloy had only a slight decrease in hot ductility in comparison to commercial INCONEL alloy 601.
  • the first series of tests containing the compositions listed below in Table 4 was prepared.
  • the series of 12.5 kg cast ingot were machined, dressed and then forged at about 1150°C to 15 mm thick slabs. Each slab was then hot rolled at about 1150°C in stages to produce 4 mm thick hot band. Each sample was final annealed for 30 minutes at 1177°C and air cooled to room temperature. Prior to oxidation testing, the specimens were ground on silicon carbide paper to a 240 grade finish as previously provided for the samples of Table 1.
  • Table 5 on average were slightly poorer than alloy 601 at 1100°C. However, alloys of the invention provided some improvement in cyclic oxidation at 1200°C. It is believed that result of Table 5 would be improved if the stable oxide were formed by an initial oxidation treatment at a temperature of at least 1100°C prior to testing.
  • Oxidation penetration was also tested for alloys of the invention and alloy 601. Oxidation penetration test result data are given below in Table 7.
  • Nickel in an amount of 55-65% provides workability, fabricability and general oxidation resistance to the alloy. Chromium in an amount of 19-25% provides oxidation resistance. Oxidation resistance is insufficient at less than 19% chromium. At chromium levels above 25 %, deleterious chromium phases may form. Initial testing has indicated that chromium levels above 20% have a neutral effect and do not contribute additional oxidation resistance. Aluminum is beneficial to oxidation properties and increased aluminum is believed to contribute to adherence of the oxide scale. Aluminum in an amount of at least 1 % or most advantageously at least 2.7% provides high temperature oxidation resistance. Aluminum is limited to 4.5% (preferably 3.5%) to limit adverse hot workability effects.
  • Yttrium in an amount of at least 0.045% and preferably at least 0.05% contributes to stabilizing the oxide.
  • Yttria was not readily visible with optical microscopy in the samples tested. Excess yttrium (above 0.3%) is believed to adversely affect hot workability and welding properties. Most advantageously yttrium is limited to 0.07%.
  • Titanium is added as a reactive element to combine with nitrogen and carbon. At least 0.15 % titanium is added for tying up nitrogen. Excess titanium above 1 % adversely affects oxidation resistance and workability. Iron acts as an inexpensive substitute for nickel. Most advantageously at least 10% iron is present to lower the cost of the alloy. Furthermore, iron is most advantageously limited to 20 or 18% to limit reduction of nickel's beneficial properties. Carbon in an amount of 0.005% or preferably 0.01 % provides adequate grain size control. An upper limit of 0.5 % carbon or preferably 0.29 carbon is maintained to limit excessive carbide formation that ties up useful element and to limit grain boundary embrittlement. At least 0.1% silicon and advantageously 0.5% silicon is added for oxidation resistance. Silicon is limited to 1.5% or preferably 1% to limit weldability and workability problems.
  • Manganese is an impurity that adversely impacts oxidation resistance.
  • manganese is limited to 1% and most advantageously manganese is limited to 0.5%.
  • at least 0.005% total magnesium, calcium and/or cerium are added for improved malleability and deoxidation.
  • Total magnesium and/or calcium is advantageously limited to 0.5% and most advantageously 0.2% to minimize adverse effects upon weldability and workability.
  • Boron in an amount of 0.0001% or preferably 0.001 % provides improved malleability. Boron is limited to 0.1% to minimize adverse effect upon malleability and weldability.
  • boron is limited to 0.05% and most advantageously boron is limited to 0.01% or 0.006%.
  • Zirconium may optionally be added for malleability and grain size control. Zirconium reacts with nitrogen to form nitrides that inhibit grain growth at elevated temperature. Zirconium is limited to 0.5% and most advantageously 0.2% to limit adverse effects upon weldability and workability. Similarly, nitrogen is added to provide an effective amount of grain growth resistance. Nitrogen, typically is provided in sufficient quantity as an impurity of raw materials. A quantity of at least 0.0001% nitrogen or 0.001 % nitrogen provides resistance against grain growth. Most advantageous grain growth control may be obtained by maintaining a level of at least 0.03 % nitrogen. Alternatively, grain growth may be controlled by limiting stored energy in the alloy by additional annealing steps between deformation processes. Nitrogen is limited to 0.2 % to avoid excess internal oxidation of beneficial elements. Nitrogen is advantageously limited and most advantageously to 0.1 % and 0.05% respectively.
  • Cerium in an amount up to 1% may optionally be added as a magnesium substitute or for additional oxidation resistance.
  • cerium is not necessary for oxidation resistance.
  • Cobalt is an impurity acceptable in quantities up to 10% that acts as a substitute for nickel.
  • cobalt is limited to 5% and most advantageously cobalt is maintained below 1 %. Due to the relatively high cost of cobalt, cobalt is preferably not deliberately added. Copper, molybdenum, niobium, vanadium and tungsten are advantageously held to the limits of Table 8 to improve appearance of the alloy.
  • copper, molybdenum, niobium, vanadium and tungsten are held as low as commercially practical.
  • Lead, tin, antimony, bismuth, phosphorous, sulfur and oxygen are all incidental impurities maintained at levels as low as commercially practical.
  • the total lead, tin, antimony, bismuth, phosphorous, sulfur plus oxygen level is maintained below 0.1 %.
  • alloy of the invention was tested to provide acceptable mechanical properties. Initial welding tests indicated a tendency for solidification cracking linked to increased yttrium content. However, the tests were not performed on alloys of the invention. Alloys of the invention are readily fabricated in seamless tubes by conventional extrusion or extrusion and cold working techniques. The tubes are then cut into short length rollers especially useful for kilns having operating temperatures around 1200°C.
  • the oxide formed at high temperature is extremely adherent and less prone to discoloration of ceramics than conventional alloy 601.
  • the adherent scale is especially useful for white ceramics.

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Abstract

The invention provides a heat and corrosion resistant alloy having, by weight percent, 55-65% nickel, 19-25% chromium, 1-4.5% aluminum, 0.045-0.3% yttrium, 0.15-1% titanium, 0.005-0.5% carbon, 0.1-1.5% silicon, 0-1% manganese, at least 0.005% total magnesium, calcium and/or cerium, less than 0.5% total magnesium and/or calcium, less than 1% cerium, 0.0001-0.1% boron, 0-0.5% zirconium, 0.0001-0.1% nitrogen, 0-10% cobalt and balance, iron and incidental impurities.

Description

    FIELD OF INVENTION
  • This invention is related to the field of Ni-Cr-Fe alloys and particularly to alloys used in high temperature (1200°C) applications.
  • BACKGROUND OF THE INVENTION
  • Ni-Cr-Fe alloys such as INCONEL® alloy 601 have historically been used for general-purpose engineering applications requiring heat and corrosion resistance. (INCONEL is a registered trademark of the Inco family of companies.) In addition, INCONEL alloy 601 has excellent resistance to thermal cycle fatigue in combination with high temperature oxidation resistance. Commercial uses of INCONEL alloy 601 include thermal processing equipment, chemical processing applications, petrochemical applications, pollution control applications and turbine engine components.
  • INCONEL alloy 601 has been widely used as a roller alloy for applications within high temperature kilns used in firing of ceramic tiles. In high temperature kilns used for firing ceramics, rollers are typically exposed to oxidizing conditions at temperatures as high as 1000°C or 1165°C. At such high temperatures, roller alloys have a tendency to slowly fail due to gradual oxidation. At increased temperatures of about 1200°C, oxidation rate and spalling rate increase unacceptably.
  • It is the object of this invention to provide a Ni-Cr-Fe alloy with improved resistance to oxidation at 1200°C.
  • SUMMARY OF THE INVENTION
  • The invention provides a heat and corrosion resistant alloy having, by weight percent, 55-65% nickel, 19-25% chromium, 1-4.5% aluminum, 0.045-0.3% yttrium, 0.15-1% titanium, 0.005-0.5% carbon, 0.1-1.5% silicon, 0-1% manganese, at least 0.005% total magnesium, calcium and/or cerium, less than 0.5% total magnesium and/or calcium, less than 1% cerium, 0.0001-0.1% boron, 0-0.5% zirconium, 0.0001-0.1% nitrogen, 0-10% cobalt and balance iron and incidental impurities.
  • DESCRIPTION OF THE DRAWINGS
  • Figure 1 is a plot of mass change versus time for various alloys in an air atmosphere at 1165°C.
  • Figure 2 is a plot of mass charge versus time for various alloys in an air atmosphere at 1200°C.
  • DESCRIPTION OF PREFERRED EMBODIMENT
  • The invention provides a Ni-Cr-Fe-Al alloy with improved high temperature cyclic oxidation resistance. A nickel-base alloy containing a combination of chromium, yttrium, silicon and aluminum has been found to dramatically improve oxidation resistance at 1200°C. The 1200°C temperature is particularly useful for kilns used for firing lead-free frits.
  • INITIAL TEST
  • A total of six test heats of Ni-Cr-Fe alloys were cast into 10 kg ingots. Ingot 7 originated from a commercial heat. Chemical compositions of the test heats expressed in weight percent are given below in Table 1. (All compositions in this specification are expressed in weight percent unless specifically indicated.)
  • TABLE 1
  • Ingot numbers 1-6 represent experimental heats; and Ingot number 7 represents an alloy within the commercial range of INCONEL alloy 601. The ingots were machined, dressed and forged at 1140°C into 50.8 mm round bars. The round bars were annealed at 1175°C for 30 minutes. Test coupons were machined from forged bar into plates having approximate dimensions of 15 mm x 20 mm x 3 mm. Plates were pierced with a 3 mm diameter hole for poaching the coupon to a jig. All oxidation test specimens were polished with silicon carbide paper to a 240 grade finish. Following recordation of sample size, all test samples were degreased and dried in hot air. The test specimens were given a cyclic oxidation test of 168 hours in a 1200°C air atmosphere furnace followed by a 20 minutes cooling cycle. Results from the cyclic oxidation test are given below in Table 2.
    Figure imgb0001
    Figure imgb0002
  • The above sample numbers correspond to the ingot numbers of Table 1. From the above high temperature experiment it was determined that the composition of ingot 4 at 1200°C provided the best oxidation resistance. Scale integrity was found to increase with decreased amounts of titanium. Segregation of yttrium rich phases at the alloy/scale interface was found to increase scale adhesion and may have an effect in modifying alloy oxidation mechanism leading to improved oxidation resistance. The tightly adherent scale layer of high yttrium sample number 4 was found to provide an effective barrier for preventing internal oxidation. In addition, the increased aluminum content of sample number 4 was believed to also contribute high temperature stability of the oxide scale.
  • From the above results, a commercial heat of Ni-Cr-Fe-Al alloy (Alloy A) having the ranges of Table 3 was prepared. TABLE 3
    ELEMENT MAXIMUM AIM MINIMUM ACTUAL
    C 0.050 0.040 - 0.032
    Si 0.79 0.70 0.50 0.78
    Mn 1.00 0.25 0.10 0.31
    P .015 - - 0.010
    S .015 - - 0.001
    Al 3.00 2.70 2.50 2.63
    Co 1.00 - - 0.02
    Cr 23.00 21.00 20.00 20.59
    Cu 0.50 - - <0.01
    Fe 18.0 BAL - 14.9
    Mg 0.019 0.017 0.01 0.015
    Mo 0.50 - - <0.01
    Nb 0.30 - - <0.01
    Ni 63.00 60.0 58.0 60.25
    Ti 0.25 0.23 0.21 0.26
    B (ppm) 60 34 30 40
    Y 0.15 0.13 0.10 0.08
    V 0.10 - - 0.03
    W 0.10 - - <0.05
    N 0.1 - - 0.033
  • The invention of Alloy A provided a Ni-Cr-Fe-Al alloy with improved high temperature (1200°C) oxidation resistance. A combination of chromium, yttrium, silicon and aluminum was found to dramatically improve oxidation resistance. The improved Ni-Cr -Fe-Al alloy had only a slight decrease in hot ductility in comparison to commercial INCONEL alloy 601.
  • To verify and optimize the compositional ranges for Alloy A, a series of test heats was prepared and analyzed.
  • EXAMPLE
  • The first series of tests containing the compositions listed below in Table 4 was prepared. The series of 12.5 kg cast ingot were machined, dressed and then forged at about 1150°C to 15 mm thick slabs. Each slab was then hot rolled at about 1150°C in stages to produce 4 mm thick hot band. Each sample was final annealed for 30 minutes at 1177°C and air cooled to room temperature. Prior to oxidation testing, the specimens were ground on silicon carbide paper to a 240 grade finish as previously provided for the samples of Table 1.
  • TABLE 4
  • In the initial series of cyclic oxidation tests, the alloys of Table 4 were exposed to a repetitive thermal cycle of 20 minutes heating followed by 10 minutes cooling in an atmosphere with the resulting weight changes provided in Table 5.
    Figure imgb0003
    Figure imgb0004
  • The examples of Table 5 on average were slightly poorer than alloy 601 at 1100°C. However, alloys of the invention provided some improvement in cyclic oxidation at 1200°C. It is believed that result of Table 5 would be improved if the stable oxide were formed by an initial oxidation treatment at a temperature of at least 1100°C prior to testing.
  • The alloys of Table 4 were then exposed to an air atmosphere for one week periods followed by a 20 minute room temperature air cooling. Result of the one week cycle tests are provided in Table 6.
    Figure imgb0005
  • At temperatures of 1050°C alloys of the invention provided a mixed effect upon the longer cycle duration tests. However, at 1165 °C and 1200°C, oxidation resistance was dramatically improved. Figures 1 and 2 illustrate this improvement. The alloys of the invention initially oxidize at a greater rate than alloy 601. An advantage to the alloys is the steady state low oxidation rate achieved after/during the first week of exposure. For optimum results, the alloy should be held at a temperature of at least 1100°C for sufficient time to enable the stable adherent oxide to form prior to service.
  • Oxidation penetration was also tested for alloys of the invention and alloy 601. Oxidation penetration test result data are given below in Table 7.
    Figure imgb0006
  • Data of Table 7 indicate good resitance to oxide penetration for alloys of the invention.
  • From he above test the ranges below in Table 8 were determined to define ranges of the alloy of the invention.
    Figure imgb0007
  • Nickel in an amount of 55-65% provides workability, fabricability and general oxidation resistance to the alloy. Chromium in an amount of 19-25% provides oxidation resistance. Oxidation resistance is insufficient at less than 19% chromium. At chromium levels above 25 %, deleterious chromium phases may form. Initial testing has indicated that chromium levels above 20% have a neutral effect and do not contribute additional oxidation resistance. Aluminum is beneficial to oxidation properties and increased aluminum is believed to contribute to adherence of the oxide scale. Aluminum in an amount of at least 1 % or most advantageously at least 2.7% provides high temperature oxidation resistance. Aluminum is limited to 4.5% (preferably 3.5%) to limit adverse hot workability effects. Yttrium in an amount of at least 0.045% and preferably at least 0.05% contributes to stabilizing the oxide. Yttria was not readily visible with optical microscopy in the samples tested. Excess yttrium (above 0.3%) is believed to adversely affect hot workability and welding properties. Most advantageously yttrium is limited to 0.07%.
  • Titanium is added as a reactive element to combine with nitrogen and carbon. At least 0.15 % titanium is added for tying up nitrogen. Excess titanium above 1 % adversely affects oxidation resistance and workability. Iron acts as an inexpensive substitute for nickel. Most advantageously at least 10% iron is present to lower the cost of the alloy. Furthermore, iron is most advantageously limited to 20 or 18% to limit reduction of nickel's beneficial properties. Carbon in an amount of 0.005% or preferably 0.01 % provides adequate grain size control. An upper limit of 0.5 % carbon or preferably 0.29 carbon is maintained to limit excessive carbide formation that ties up useful element and to limit grain boundary embrittlement. At least 0.1% silicon and advantageously 0.5% silicon is added for oxidation resistance. Silicon is limited to 1.5% or preferably 1% to limit weldability and workability problems.
  • Manganese is an impurity that adversely impacts oxidation resistance. Advantageously, manganese is limited to 1% and most advantageously manganese is limited to 0.5%. Most advantageously, at least 0.005% total magnesium, calcium and/or cerium are added for improved malleability and deoxidation. Total magnesium and/or calcium is advantageously limited to 0.5% and most advantageously 0.2% to minimize adverse effects upon weldability and workability. Boron in an amount of 0.0001% or preferably 0.001 % provides improved malleability. Boron is limited to 0.1% to minimize adverse effect upon malleability and weldability. Advantageously, boron is limited to 0.05% and most advantageously boron is limited to 0.01% or 0.006%. Zirconium may optionally be added for malleability and grain size control. Zirconium reacts with nitrogen to form nitrides that inhibit grain growth at elevated temperature. Zirconium is limited to 0.5% and most advantageously 0.2% to limit adverse effects upon weldability and workability. Similarly, nitrogen is added to provide an effective amount of grain growth resistance. Nitrogen, typically is provided in sufficient quantity as an impurity of raw materials. A quantity of at least 0.0001% nitrogen or 0.001 % nitrogen provides resistance against grain growth. Most advantageous grain growth control may be obtained by maintaining a level of at least 0.03 % nitrogen. Alternatively, grain growth may be controlled by limiting stored energy in the alloy by additional annealing steps between deformation processes. Nitrogen is limited to 0.2 % to avoid excess internal oxidation of beneficial elements. Nitrogen is advantageously limited and most advantageously to 0.1 % and 0.05% respectively.
  • Cerium in an amount up to 1% may optionally be added as a magnesium substitute or for additional oxidation resistance. However, with the chromium, aluminum, silicon and yttrium ranges of the invention cerium is not necessary for oxidation resistance. Cobalt is an impurity acceptable in quantities up to 10% that acts as a substitute for nickel. Advantageously, cobalt is limited to 5% and most advantageously cobalt is maintained below 1 %. Due to the relatively high cost of cobalt, cobalt is preferably not deliberately added. Copper, molybdenum, niobium, vanadium and tungsten are advantageously held to the limits of Table 8 to improve appearance of the alloy. Most advantageously, copper, molybdenum, niobium, vanadium and tungsten are held as low as commercially practical. Lead, tin, antimony, bismuth, phosphorous, sulfur and oxygen are all incidental impurities maintained at levels as low as commercially practical. Most advantageously, the total lead, tin, antimony, bismuth, phosphorous, sulfur plus oxygen level is maintained below 0.1 %.
  • The alloy of the invention was tested to provide acceptable mechanical properties. Initial welding tests indicated a tendency for solidification cracking linked to increased yttrium content. However, the tests were not performed on alloys of the invention. Alloys of the invention are readily fabricated in seamless tubes by conventional extrusion or extrusion and cold working techniques. The tubes are then cut into short length rollers especially useful for kilns having operating temperatures around 1200°C.
  • The oxide formed at high temperature is extremely adherent and less prone to discoloration of ceramics than conventional alloy 601. The adherent scale is especially useful for white ceramics.
  • While in accordance with the provisions of the statute, there is illustrated and described herein specific embodiments of the invention. Those skilled in the art will understand that changes may be made in die form of the invention covered by the claims and the certain features of the invention may sometimes be used to advantage without a corresponding use of the other features.

Claims (12)

1. A heat and corrosion resistant alloy consisting essentially of, in weight percent, about 55-65% nickel, about 19-25% chromium, about 1-4.5% aluminum, 0.045-0,3% yttrium, about 0.15-1% titanium, about 0.005-0.5% carbon, about 0.1-1.5% silicon, about 0-1% manganese, at least about 0.005% total of at least one element selected from the group consisting of magnesium, calcium and cerium, less than about 0.5% total magnesium plus calcium, less than about 1 % cerium, about 0.0001-0.1 % boron, about 0-0.5 % zirconium, about 0.0001-0.2% nitrogen, about 0-10% cobalt and balance iron and incidental impurities.
2. The alloy of claim 1 wherein said chromium is about 19-22 %, said aluminum is about 2.5-4.0 %, said yttrium is about 0.05-0.15 %, said titanium is about 0.15-0.75% and said silicon is about 0.5-1 %.
3. The alloy of claim 1 wherein said carbon is about 0.01-0.3%, said magnesium is about 0.005-0.2%, said boron is about 0.001-0.05% and said nitrogen is about 0.01-0.1 %.
4 A heat and corrosion resistant alloy consisting essentially of, in weight percent, about 57.5-62.5% nickel, about 19-22% chromium, about 2.5-4% aluminum, about 0.05-0.15% yttrium, about 0.15-0.75% titanium, about 0.01-0.3% carbon, about 0.5-1% silicon, about 0-1% manganese, at least about 0.005% total at least one element selected from the group consisting of magnesium, calcium and cerium, less than about 0.2% total magnesium plus calcium, less than about 1 % cerium, about 0.001-0.05% boron, about 0-0.4% zirconium, about 0-5% cobalt and balance iron and incidental impurities.
5 The alloy of claim 4 wherein said chromium is about 19.5-21%, said aluminum is about 2.7-3.5 %, said yttrium is about 0.05-0.07% and said titanium is about 0.3-0.75%.
6. The alloy of claim 4 wherein said carbon is about 0.05-0.15%, said magnesium is about 0.005-0.2 %, said boron is about 0.01-0.01 % and said nitrogen is about 0,001-0.05%.
7 The alloy of any one of claims 1 to 6 wherein said iron is less than about 20%, e.g. 10-18%.
8 The alloy of claim 4 wherein said alloy includes about 0-0.5 % copper, about 0-0.5% molybdenum, about 0-0.3% niobium, about 0-0.1% vanadium and about 0-0.1% tungsten.
9 A heat and corrosion resistant alloy consisting essentially of about 57.5-62.5% nickel, about 19.5-21% chromium, about 2.7-3.5 aluminum, about 0.05-0.07% yttrium, about 0.3-0.75% titanium, about 10-18% iron, about 0.5-1% silicon, about 0-0.5% manganese, at least about 0.005% total at least one element selected from the group consisting of magnesium, calcium and cerium, less than about 0.2% total magnesium plus calcium, less than about 1% cerium, about 0.001-0.01 % boron, about 0-0.2% zirconium, about 0.001-0.05% nitrogen, about 0-1% cobalt and incidental impurities.
10 The alloy of claim 9 wherein said alloy includes about 0-0.5% copper, about 0-0.5 % molybdenum, about 0-0.3 % niobium, about 0-0.1 % vanadium and about 0.01% tungsten.
11 The alloy of claim 9 wherein said alloy contains less than about 0.1% total lead, tin, antimony, bismuth, phosphorous, sulfur and oxygen.
12 The alloy of claim 9 wherein said nitrogen is at least 0.03%.
EP92311611A 1991-12-20 1992-12-18 High temperature resistant Ni-Cr alloy Revoked EP0549286B1 (en)

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US81258491A 1991-12-20 1991-12-20
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Cited By (24)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0752481A1 (en) * 1995-07-04 1997-01-08 Krupp VDM GmbH Malleable nickel alloy
US5997809A (en) * 1998-12-08 1999-12-07 Inco Alloys International, Inc. Alloys for high temperature service in aggressive environments
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EP2072627A1 (en) 2007-12-12 2009-06-24 Haynes International, Inc. Weldable oxidation resistant nickel-iron-chromium-aluminum alloy
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DE102012002514A1 (en) 2011-02-23 2012-08-23 Thyssenkrupp Vdm Gmbh Nickel-chromium-iron-aluminum alloy with good processability
DE102012011162A1 (en) 2012-06-05 2013-12-05 Outokumpu Vdm Gmbh Nickel-chromium alloy with good processability, creep resistance and corrosion resistance
WO2014023274A1 (en) 2012-08-10 2014-02-13 Outokumpu Vdm Gmbh Usage of a nickel-chromium-iron-aluminium alloy with good workability
CN104827206A (en) * 2015-05-09 2015-08-12 芜湖鼎恒材料技术有限公司 Ni-Cr-Al nanometer welding layer and preparation method
US9551051B2 (en) 2007-12-12 2017-01-24 Haynes International, Inc. Weldable oxidation resistant nickel-iron-chromium aluminum alloy
US9657373B2 (en) 2012-06-05 2017-05-23 Vdm Metals International Gmbh Nickel-chromium-aluminum alloy having good processability, creep resistance and corrosion resistance
DE102018107248A1 (en) 2018-03-27 2019-10-02 Vdm Metals International Gmbh USE OF NICKEL CHROME IRON ALUMINUM ALLOY
WO2021110217A1 (en) 2019-12-06 2021-06-10 Vdm Metals International Gmbh Nickel-chromium-iron-aluminum alloy having good processability, creep resistance and corrosion resistance, and use thereof
CN114231795A (en) * 2021-12-23 2022-03-25 佛山市天禄智能装备科技有限公司 Preparation method of high-temperature-resistant alloy for rotary kiln and rotary kiln body
CN115717205A (en) * 2021-08-24 2023-02-28 深圳市卓亮迪科技有限公司 A kind of high-temperature high-resistance nickel-based alloy and its preparation method
CN118006968A (en) * 2024-04-08 2024-05-10 无锡市雪浪合金科技有限公司 Nickel-based superalloy and preparation method thereof
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EP0752481A1 (en) * 1995-07-04 1997-01-08 Krupp VDM GmbH Malleable nickel alloy
US5755897A (en) * 1995-07-04 1998-05-26 Krupp Vdm Gmbh Forgeable nickel alloy
US5997809A (en) * 1998-12-08 1999-12-07 Inco Alloys International, Inc. Alloys for high temperature service in aggressive environments
WO2000034541A1 (en) * 1998-12-09 2000-06-15 Inco Alloys International, Inc. High strength alloy tailored for high temperature mixed-oxidant environments
US6287398B1 (en) 1998-12-09 2001-09-11 Inco Alloys International, Inc. High strength alloy tailored for high temperature mixed-oxidant environments
RU2169783C2 (en) * 1999-06-02 2001-06-27 ОАО "Научно-производственное объединение энергетического машиностроения им. акад. В.П. Глушко" Heat resistant-weldable nickel based-alloy
GB2361933A (en) * 2000-05-06 2001-11-07 British Nuclear Fuels Plc Melting crucible made from a nickel-based alloy
FR2808537A1 (en) * 2000-05-06 2001-11-09 British Nuclear Fuels Plc FUSION CUP
WO2004067788A1 (en) * 2003-01-25 2004-08-12 Schmidt + Clemens Gmbh + Co. Kg Thermostable and corrosion-resistant cast nickel-chromium alloy
EA008522B1 (en) * 2003-01-25 2007-06-29 Шмидт+Клеменс Гмбх+Ко. Кг Themostable and corrosion-resistant cast nichel-chromium alloy
US10724121B2 (en) 2003-01-25 2020-07-28 Schmidt + Clemens Gmbh + Co. Kg Thermostable and corrosion-resistant cast nickel-chromium alloy
US10041152B2 (en) 2003-01-25 2018-08-07 Schmidt + Clemens Gmbh + Co. Kg Thermostable and corrosion-resistant cast nickel-chromium alloy
RU2256717C1 (en) * 2004-06-25 2005-07-20 Федеральное государственное унитарное предприятие "Всероссийский научно-исследовательский институт авиационных материалов" (ФГУП "ВИАМ") High-temperature nickel-based weldable alloy and article made from this alloy
EP1780295A4 (en) * 2004-08-02 2012-04-04 Sumitomo Metal Ind FIXED JOINT AND WELDING MATERIAL THEREOF
WO2007004973A1 (en) 2005-07-01 2007-01-11 Sandvik Intellectual Property Ab Ni-cr-fe alloy for high-temperature use.
EP1899489A4 (en) * 2005-07-01 2010-08-18 Sandvik Intellectual Property Ni-cr-fe alloy for high-temperature use.
KR101322091B1 (en) * 2005-07-01 2013-10-25 산드빅 인터렉츄얼 프로퍼티 에이비 Ni-Cr-Fe ALLOY FOR HIGH-TEMPERATURE USE
US8926769B2 (en) 2005-07-01 2015-01-06 Sandvik Intellectual Property Ab Ni—Cr—Fe alloy for high-temperature use
US9551051B2 (en) 2007-12-12 2017-01-24 Haynes International, Inc. Weldable oxidation resistant nickel-iron-chromium aluminum alloy
EP2072627A1 (en) 2007-12-12 2009-06-24 Haynes International, Inc. Weldable oxidation resistant nickel-iron-chromium-aluminum alloy
US8506883B2 (en) 2007-12-12 2013-08-13 Haynes International, Inc. Weldable oxidation resistant nickel-iron-chromium-aluminum alloy
AU2009318183B2 (en) * 2008-11-19 2014-04-10 Sandvik Intellectual Property Ab Aluminium oxide forming nickel based alloy
WO2010059105A1 (en) * 2008-11-19 2010-05-27 Sandvik Intellectual Property Ab Aluminium oxide forming nickel based alloy
US20110045362A1 (en) * 2009-08-24 2011-02-24 Staxera Gmbh Oxidation-resistant composite conductor and manufacturing method for the composite conductor
RU2568547C2 (en) * 2011-02-23 2015-11-20 Оутокумпу Вдм Гмбх Nickel-chromium-iron-aluminium alloy with good machinability
DE102012002514A1 (en) 2011-02-23 2012-08-23 Thyssenkrupp Vdm Gmbh Nickel-chromium-iron-aluminum alloy with good processability
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US9476110B2 (en) 2011-02-23 2016-10-25 Vdm Metals International Gmbh Nickel—chromium—iron—aluminum alloy having good processability
DE102012002514B4 (en) * 2011-02-23 2014-07-24 VDM Metals GmbH Nickel-chromium-iron-aluminum alloy with good processability
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DE102012011162A1 (en) 2012-06-05 2013-12-05 Outokumpu Vdm Gmbh Nickel-chromium alloy with good processability, creep resistance and corrosion resistance
US9650698B2 (en) 2012-06-05 2017-05-16 Vdm Metals International Gmbh Nickel-chromium alloy having good processability, creep resistance and corrosion resistance
US9657373B2 (en) 2012-06-05 2017-05-23 Vdm Metals International Gmbh Nickel-chromium-aluminum alloy having good processability, creep resistance and corrosion resistance
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DE102012015828B4 (en) * 2012-08-10 2014-09-18 VDM Metals GmbH Use of a nickel-chromium-iron-aluminum alloy with good processability
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CN104827206A (en) * 2015-05-09 2015-08-12 芜湖鼎恒材料技术有限公司 Ni-Cr-Al nanometer welding layer and preparation method
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