CA3093022C - Corrosion resistant alloy - Google Patents
Corrosion resistant alloy Download PDFInfo
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- CA3093022C CA3093022C CA3093022A CA3093022A CA3093022C CA 3093022 C CA3093022 C CA 3093022C CA 3093022 A CA3093022 A CA 3093022A CA 3093022 A CA3093022 A CA 3093022A CA 3093022 C CA3093022 C CA 3093022C
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- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C19/00—Alloys based on nickel or cobalt
- C22C19/03—Alloys based on nickel or cobalt based on nickel
- C22C19/05—Alloys based on nickel or cobalt based on nickel with chromium
- C22C19/051—Alloys based on nickel or cobalt based on nickel with chromium and Mo or W
- C22C19/055—Alloys based on nickel or cobalt based on nickel with chromium and Mo or W with the maximum Cr content being at least 20% but less than 30%
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22F—CHANGING THE PHYSICAL STRUCTURE OF NON-FERROUS METALS AND NON-FERROUS ALLOYS
- C22F1/00—Changing the physical structure of non-ferrous metals or alloys by heat treatment or by hot or cold working
- C22F1/10—Changing the physical structure of non-ferrous metals or alloys by heat treatment or by hot or cold working of nickel or cobalt or alloys based thereon
Abstract
The invention relates to metallurgy and more particularly to nickel-based alloys intended for use in aggressive oxidising environments. The present nickel-based corrosion-resistant alloy contains: = 0.006 wt.% carbon, = 0.1 wt.% silicon, = 1.0 wt.% manganese, 22.8-24.0 wt.% chromium, = 0.75 wt.% iron, 12.0-14.0 wt.% molybdenum, 0.01-0.03 wt.% niobium, 0.01-0.06 wt.% titanium, 0.1-0.2 wt.% aluminium, 0.005-0.01 wt.% magnesium, = 0.015 wt.% phosphorus and < 0.012 wt.% sulphur, with the remainder being nickel and unavoidable impurities.
Description
Corrosion resistant alloy The invention relates to metallurgic engineering, to nickel-based alloys intended for use in aggressive oxidizing environments.
A corrosion-resistant alloy Nicrofer 6616 hMo alloy C-4 (No. 2.4610), containing wt.%: 14.5-17.5 Cr, 14.0-17.0 Mo, <3.0 Fe, <0.009 C, <1.0 Mn, <0.05 Si, <2.0 Co, <0.7 Ti, <0.020 P, <0.010 S, nickel and other unavoidable impurities is known from the prior art (Catalogue "Corrosion-resistant, heat-resistant and high-strength steels and alloys", M., Prometey-Splav, 2008, pp. 304 ¨ 306).
The alloy is used for the manufacture of equipment operated in a wide range of chemical en-vironments, at room and elevated temperatures. In particular, for adsorbers in flue gas desulphuring;
etching baths and acid recovery plants; acetic acid and agrochemicals plants.
The nearest analogue of the given invention is an alloy XH65MBY(311760) containing, wt.%:
<0.02 C, <0.1 Si, <1.0 Mn, 14.5-16.5 Cr, 15.0-17.0 Mo, 3.0 ________________________ 1.5 W, <0.5 Fe , <0.012 S, <0.015 P, nickel and other unavoidable impurities (GOST 5632-2014 - prototype).
The alloy is used for the manufacture of welded structures (columns, heat exchangers, reactors) operating under elevated temperatures in aggressive redox environments, in the chemical, petrochem-ical industry (production of acetic acid, epoxy resins, vinyl acetate, melamine, complex organic com-pounds) and other industries in the temperature range -70 to 500 C.
The XH65MBY alloy and its welded joints can be used in KC1¨ A1C13 ¨ ZrC14 media only up to 500 C, because at a temperature above this value, the alloy, in addition to intergranular corro-sion and corrosion cracking, sharply decreases the percentage elongation from 48% to 7.3-13% at 550 C and up to 2.5% at 625 C and the embrittlement of the metal appears when deformation is applied.
The objective of the invention is to create an alloy having a high level of corrosion properties at temperatures up to T = 650 C in the working media of chloride plants (KCl AlC13 ¨ ZrC14).
The technical result of the invention is to obtain an alloy with a high level of plastic properties for the operation in the temperature range 550 C to 625 C and increased corrosion cracking resistance in chlorides KC1, AlC13 + (ZrC14 HfC14) molten metal, at temperatures up to 650 C.
The specified technical result is achieved in that the alloy containing carbon, silicon, manga-nese, chromium, molybdenum, phosphorus, sulphur, iron, nickel and unavoidable impurities, Date Recue/Date Received 2022-08-12 according to the invention additionally contains titanium, aluminium, niobium, magnesium with the following components ratio, wt.% :
Carbon <0.006 Silicon <0.1 Manganese <1.0 Chromium 22.8-24.0 Iron <0.75 Molybdenum 12.0-14.0 Niobium 0.01-0.03 Titanium 0.01-0.06 Aluminium 0.1-0.2 Magnesium 0.005-0.01 Phosphorus <0.015 Sulphur <0.012 Nickel and unavoidable impurities balance To obtain a stable structure and plastic properties, it is preferable that the content of chro-[Cr]+[Mo]
mium, molybdenum and iron is related by the ratio: > 46,4 (1) (the ratio of the total [Fe] ¨
weight percentage of chromium and molybdenum to the percentage of iron is not less than 46.4) To obtain a stable structure and high corrosion properties, it is preferable that the content of niobium and carbon is related by the ratio:
[Nb]
[C]66
A corrosion-resistant alloy Nicrofer 6616 hMo alloy C-4 (No. 2.4610), containing wt.%: 14.5-17.5 Cr, 14.0-17.0 Mo, <3.0 Fe, <0.009 C, <1.0 Mn, <0.05 Si, <2.0 Co, <0.7 Ti, <0.020 P, <0.010 S, nickel and other unavoidable impurities is known from the prior art (Catalogue "Corrosion-resistant, heat-resistant and high-strength steels and alloys", M., Prometey-Splav, 2008, pp. 304 ¨ 306).
The alloy is used for the manufacture of equipment operated in a wide range of chemical en-vironments, at room and elevated temperatures. In particular, for adsorbers in flue gas desulphuring;
etching baths and acid recovery plants; acetic acid and agrochemicals plants.
The nearest analogue of the given invention is an alloy XH65MBY(311760) containing, wt.%:
<0.02 C, <0.1 Si, <1.0 Mn, 14.5-16.5 Cr, 15.0-17.0 Mo, 3.0 ________________________ 1.5 W, <0.5 Fe , <0.012 S, <0.015 P, nickel and other unavoidable impurities (GOST 5632-2014 - prototype).
The alloy is used for the manufacture of welded structures (columns, heat exchangers, reactors) operating under elevated temperatures in aggressive redox environments, in the chemical, petrochem-ical industry (production of acetic acid, epoxy resins, vinyl acetate, melamine, complex organic com-pounds) and other industries in the temperature range -70 to 500 C.
The XH65MBY alloy and its welded joints can be used in KC1¨ A1C13 ¨ ZrC14 media only up to 500 C, because at a temperature above this value, the alloy, in addition to intergranular corro-sion and corrosion cracking, sharply decreases the percentage elongation from 48% to 7.3-13% at 550 C and up to 2.5% at 625 C and the embrittlement of the metal appears when deformation is applied.
The objective of the invention is to create an alloy having a high level of corrosion properties at temperatures up to T = 650 C in the working media of chloride plants (KCl AlC13 ¨ ZrC14).
The technical result of the invention is to obtain an alloy with a high level of plastic properties for the operation in the temperature range 550 C to 625 C and increased corrosion cracking resistance in chlorides KC1, AlC13 + (ZrC14 HfC14) molten metal, at temperatures up to 650 C.
The specified technical result is achieved in that the alloy containing carbon, silicon, manga-nese, chromium, molybdenum, phosphorus, sulphur, iron, nickel and unavoidable impurities, Date Recue/Date Received 2022-08-12 according to the invention additionally contains titanium, aluminium, niobium, magnesium with the following components ratio, wt.% :
Carbon <0.006 Silicon <0.1 Manganese <1.0 Chromium 22.8-24.0 Iron <0.75 Molybdenum 12.0-14.0 Niobium 0.01-0.03 Titanium 0.01-0.06 Aluminium 0.1-0.2 Magnesium 0.005-0.01 Phosphorus <0.015 Sulphur <0.012 Nickel and unavoidable impurities balance To obtain a stable structure and plastic properties, it is preferable that the content of chro-[Cr]+[Mo]
mium, molybdenum and iron is related by the ratio: > 46,4 (1) (the ratio of the total [Fe] ¨
weight percentage of chromium and molybdenum to the percentage of iron is not less than 46.4) To obtain a stable structure and high corrosion properties, it is preferable that the content of niobium and carbon is related by the ratio:
[Nb]
[C]66
(2) (the ratio of the weight percentage of niobium to the weight percentage of carbon is not less than 1.66).
It is preferably that the content of chromium, molybdenum, iron, niobium and carbon is related by the ratios:
[Cr]+[Mo]
> 46,4 (1) [Fe] ¨
[Nb]
________________ >1,66 At [c] (2).
Comparative analysis with the prototype allows making a conclusion that the claimed alloy differs from the known one with a lower carbon content (<0.006% instead of <0.02), molybdenum Date Regue/Date Received 2022-08-12 (12.0-14.0% instead of 15.0-17.0%), increased chromium content (23.0-24.0%
instead of 14.5-16.5%), iron (<0.75% instead of <0.5%) does not contain tungsten, as well as with the additional introduction of elements such as niobium in an amount of 0.01-0.03%, titanium in an amount of 0.01-0.06%, aluminium in an amount of 0.1-0.2% and magnesium in an amount of 0.005-0.01%.
Moreover, in particular cases of the invention, the claimed ratios of elements are observed:
[cr]+[mo]
> 46,4;
[Fe]
or [Nb] >1,66 [C]
[Nb]
1, 66 Or [Cr] +[Mo] [C]
> 46,4 at [Fe]
The limits of the content of alloying elements in the invention alloy are specified as a result of a study of alloys properties with different composition options.
Exceeding the carbon content of more than 0.006% leads to a decrease in corrosion resistance in solutions of zirconium and hafnium salts due to an increase in the carbide formation process at high temperatures (the appearance of undesirable carbide phases).
The chromium content was found to be 22.8 - 24.0% to ensure the required heat resistance in hafnium and zirconium oxides. When chromium is introduced into the alloy in the amount of less than 22.8%, the required heat resistance is not ensured, and exceeding the content above 24.0% impairs the heat resistance of the alloy.
The introduction of molybdenum into nickel alloys increases the recrystallization temperature of solid solutions, inhibits their softening, increases heat resistance, and leads to an ductility increase during short and long tests.
The range of molybdenum content of 12.0-14.0% is selected to provide the required mechan-ical properties for both short-term and long-term loads and high temperatures.
With the introduction of less than 12.0% of molybdenum, the mechanical properties are not met. When the content is above 14.0%, there is a decrease in ductility and, accordingly, a decrease in the processability of the alloy during metallurgical processing.
Niobium in an amount of 0.01-0.03%, binds residual carbon and nitrogen to carbides, nitrides and carbonitrides, prevents the formation of chromium carbides and carbonitrides along the grain boundaries. The addition of niobium in an amount 6 to 10 times higher than the carbon content in
It is preferably that the content of chromium, molybdenum, iron, niobium and carbon is related by the ratios:
[Cr]+[Mo]
> 46,4 (1) [Fe] ¨
[Nb]
________________ >1,66 At [c] (2).
Comparative analysis with the prototype allows making a conclusion that the claimed alloy differs from the known one with a lower carbon content (<0.006% instead of <0.02), molybdenum Date Regue/Date Received 2022-08-12 (12.0-14.0% instead of 15.0-17.0%), increased chromium content (23.0-24.0%
instead of 14.5-16.5%), iron (<0.75% instead of <0.5%) does not contain tungsten, as well as with the additional introduction of elements such as niobium in an amount of 0.01-0.03%, titanium in an amount of 0.01-0.06%, aluminium in an amount of 0.1-0.2% and magnesium in an amount of 0.005-0.01%.
Moreover, in particular cases of the invention, the claimed ratios of elements are observed:
[cr]+[mo]
> 46,4;
[Fe]
or [Nb] >1,66 [C]
[Nb]
1, 66 Or [Cr] +[Mo] [C]
> 46,4 at [Fe]
The limits of the content of alloying elements in the invention alloy are specified as a result of a study of alloys properties with different composition options.
Exceeding the carbon content of more than 0.006% leads to a decrease in corrosion resistance in solutions of zirconium and hafnium salts due to an increase in the carbide formation process at high temperatures (the appearance of undesirable carbide phases).
The chromium content was found to be 22.8 - 24.0% to ensure the required heat resistance in hafnium and zirconium oxides. When chromium is introduced into the alloy in the amount of less than 22.8%, the required heat resistance is not ensured, and exceeding the content above 24.0% impairs the heat resistance of the alloy.
The introduction of molybdenum into nickel alloys increases the recrystallization temperature of solid solutions, inhibits their softening, increases heat resistance, and leads to an ductility increase during short and long tests.
The range of molybdenum content of 12.0-14.0% is selected to provide the required mechan-ical properties for both short-term and long-term loads and high temperatures.
With the introduction of less than 12.0% of molybdenum, the mechanical properties are not met. When the content is above 14.0%, there is a decrease in ductility and, accordingly, a decrease in the processability of the alloy during metallurgical processing.
Niobium in an amount of 0.01-0.03%, binds residual carbon and nitrogen to carbides, nitrides and carbonitrides, prevents the formation of chromium carbides and carbonitrides along the grain boundaries. The addition of niobium in an amount 6 to 10 times higher than the carbon content in
3 Date Recue/Date Received 2022-08-12 the alloy eliminates intergranular corrosion of the alloys and protects the welds from destruction.
When the niobium content is less than 0.01%, its interaction with residual carbon is ineffective, and the niobium content above 0.03% is not reasonable for carbide formation.
Exceeding the silicon content of more than 0.1% negatively affects the processability of the alloy, as well as leads to embrittlement of the alloy due to an increase of silicon silicates content in it.
Increase of manganese content over 1.0% leads to the appearance of a fusible eutectic, which leads to the destruction of the ingot during pressure processing and reduces the heat re-sistance of the alloy, as well as leads to a decrease of local corrosion resistance.
Nickel is stable in HC1 even at boiling point. However, in the presence of chlorides, ions of Fe(111) and other oxidizing agents corrosion of nickel and nickelchrome molybdenum alloys is en-hanced, the limitation of the iron content of not more than 0.75% is due to this.
The introduction of titanium in an amount of 0.01-0.06% increases the corrosion resistance in melts of zirconium and hafnium salts, binds residual carbon to carbides and leads to the formation of a sufficient amount of Ni3Ti type intermetallic compound, which, at an operating temperature of 500-700C, positively affects the heat resistance of the alloy. When the titanium content is less than 0.01%, the requirements for corrosion resistance are not met, and the excess of the titanium content above 0.06% leads to a decrease in the processability of the alloy and the formation of undesirable phases due to the reactivity of titanium.
Aluminium and magnesium in the amount of 0.1-0.2% and 0.005-0.01% are introduced into the alloy to remove residual oxygen, as well as, with regard to aluminium, to form an intermetallic compound of the Ni3A1 type, which positively affects the heat resistance of the alloy. When these elements are introduced in amounts less than specified, the necessary removal of residual oxygen is not achieved. If the content of these elements is exceeded, gross non-metallic inclusions are formed.
When the sulphur content exceeds 0.012% and phosphorus exceeds 0.015%, coarse non-me-tallic inclusions are formed that adversely affect the ductility of the alloy.
Under the condition [C7]-F[Mo] > 46,4, when the ratio decreases below 46.4, the [Fe]
alloy structure becomes less stable (sigma phase is released), which has a negative effect on plastic characteristics and corrosion resistance.
When the niobium content is less than 0.01%, its interaction with residual carbon is ineffective, and the niobium content above 0.03% is not reasonable for carbide formation.
Exceeding the silicon content of more than 0.1% negatively affects the processability of the alloy, as well as leads to embrittlement of the alloy due to an increase of silicon silicates content in it.
Increase of manganese content over 1.0% leads to the appearance of a fusible eutectic, which leads to the destruction of the ingot during pressure processing and reduces the heat re-sistance of the alloy, as well as leads to a decrease of local corrosion resistance.
Nickel is stable in HC1 even at boiling point. However, in the presence of chlorides, ions of Fe(111) and other oxidizing agents corrosion of nickel and nickelchrome molybdenum alloys is en-hanced, the limitation of the iron content of not more than 0.75% is due to this.
The introduction of titanium in an amount of 0.01-0.06% increases the corrosion resistance in melts of zirconium and hafnium salts, binds residual carbon to carbides and leads to the formation of a sufficient amount of Ni3Ti type intermetallic compound, which, at an operating temperature of 500-700C, positively affects the heat resistance of the alloy. When the titanium content is less than 0.01%, the requirements for corrosion resistance are not met, and the excess of the titanium content above 0.06% leads to a decrease in the processability of the alloy and the formation of undesirable phases due to the reactivity of titanium.
Aluminium and magnesium in the amount of 0.1-0.2% and 0.005-0.01% are introduced into the alloy to remove residual oxygen, as well as, with regard to aluminium, to form an intermetallic compound of the Ni3A1 type, which positively affects the heat resistance of the alloy. When these elements are introduced in amounts less than specified, the necessary removal of residual oxygen is not achieved. If the content of these elements is exceeded, gross non-metallic inclusions are formed.
When the sulphur content exceeds 0.012% and phosphorus exceeds 0.015%, coarse non-me-tallic inclusions are formed that adversely affect the ductility of the alloy.
Under the condition [C7]-F[Mo] > 46,4, when the ratio decreases below 46.4, the [Fe]
alloy structure becomes less stable (sigma phase is released), which has a negative effect on plastic characteristics and corrosion resistance.
4 Date Recue/Date Received 2022-08-12 [NI)]
VI
1,66 In the condition 1-ci , with a ratio of less than 1.66, a decrease in the cor-rosion resistance of the alloy occurs.
The proposed ratio of the elements in the alloy were found experimentally and are optimal, since they allow obtaining the claimed comprehensive technical result. When breaking the ratios of the elements, the properties of the alloy deteriorate, their instability is observed, and the complex effect is not achieved.
Examples of the invention implementation.
Alloy ingots were smelted in vacuum induction furnaces. The change in the plastic properties of the studied alloys under the influence of temperatures of 550 C and 625 C
after long exposure in the furnace for more than 1000 hours was controlled by bending samples to an angle of 90 degrees or more according to GOST 14019-2003. Industrial corrosion cracking resistance tests of alloys were carried out in molten chlorides KC1, AlC13 + (ZrC14 HfC14) Table 1 shows the chemical composition of alloy ingots with various compositional op-tions, as well as the prototype alloy. Table 2 shows the results of determining the plastic properties of the alloys indicated in table 1 by bending at an angle of 90 degrees according to GUST 14019-2003. Table 3 presents the results of industrial corrosion cracking resistance tests of the alloys indi-cated in Table 1 in molten chlorides KC1, A1C13 + (ZrC14 HfC14), 100 hours, at T = 650 C.
As can be seen from tables 1, 2, the plastic properties of alloy at 550 and 625C with the claimed composition (alloys 1, 2) are higher than the properties of the prototype alloy, alloy 3, not satisfying the claimed composition, has lower plastic characteristics than alloys 1, 2 , which leads to the for-mation of cracks as a result of bending tests according to GUST 14019-2003.
As it can be seen from table 3, the corrosion rate of alloys (alloys 1, 2) that satisfy the claimed composition is lower than the corrosion rate of the prototype alloy, visual inspection did not reveal the cracks, unlike the prototype alloy. The corrosion rate of alloy 3, which does not satisfy the claimed composition, exceeds the corrosion rate of alloys 1, 2 (however, lower than the corrosion rate of the prototype alloy), visual inspection revealed a crack in the sample.
VI
1,66 In the condition 1-ci , with a ratio of less than 1.66, a decrease in the cor-rosion resistance of the alloy occurs.
The proposed ratio of the elements in the alloy were found experimentally and are optimal, since they allow obtaining the claimed comprehensive technical result. When breaking the ratios of the elements, the properties of the alloy deteriorate, their instability is observed, and the complex effect is not achieved.
Examples of the invention implementation.
Alloy ingots were smelted in vacuum induction furnaces. The change in the plastic properties of the studied alloys under the influence of temperatures of 550 C and 625 C
after long exposure in the furnace for more than 1000 hours was controlled by bending samples to an angle of 90 degrees or more according to GOST 14019-2003. Industrial corrosion cracking resistance tests of alloys were carried out in molten chlorides KC1, AlC13 + (ZrC14 HfC14) Table 1 shows the chemical composition of alloy ingots with various compositional op-tions, as well as the prototype alloy. Table 2 shows the results of determining the plastic properties of the alloys indicated in table 1 by bending at an angle of 90 degrees according to GUST 14019-2003. Table 3 presents the results of industrial corrosion cracking resistance tests of the alloys indi-cated in Table 1 in molten chlorides KC1, A1C13 + (ZrC14 HfC14), 100 hours, at T = 650 C.
As can be seen from tables 1, 2, the plastic properties of alloy at 550 and 625C with the claimed composition (alloys 1, 2) are higher than the properties of the prototype alloy, alloy 3, not satisfying the claimed composition, has lower plastic characteristics than alloys 1, 2 , which leads to the for-mation of cracks as a result of bending tests according to GUST 14019-2003.
As it can be seen from table 3, the corrosion rate of alloys (alloys 1, 2) that satisfy the claimed composition is lower than the corrosion rate of the prototype alloy, visual inspection did not reveal the cracks, unlike the prototype alloy. The corrosion rate of alloy 3, which does not satisfy the claimed composition, exceeds the corrosion rate of alloys 1, 2 (however, lower than the corrosion rate of the prototype alloy), visual inspection revealed a crack in the sample.
5 Date Recue/Date Received 2022-08-12 Table 1 - Chemical composition of the investigated alloys Ni and una-Alloy C Mn Si Mo Cr Nb S P Fe Ti Al W
voidable Ratio (1) Ratio (2) impurities Alloy 1 0.00110.55 00.7 13.0 213 0.03 0.0028 0,01 0.54 <0.01 0.1 - balance 67.2 27.27 Alloy 2 0.031 0,10 13.1 22.9 0.02 0.005 0.0050.75 0.05 0.1 - balance 48.0 3.45 Alloy 3 0.009 0.65 0.10 12.5 23.6 0.01 0.008 0.009 0.84 0.04 0.1 - balance 42.98 1.11 Alloy acc.t 0.017 0.63 0.0816.2 15.6 - 0.006 0.0090.45 - - 3.7 balance prototype
voidable Ratio (1) Ratio (2) impurities Alloy 1 0.00110.55 00.7 13.0 213 0.03 0.0028 0,01 0.54 <0.01 0.1 - balance 67.2 27.27 Alloy 2 0.031 0,10 13.1 22.9 0.02 0.005 0.0050.75 0.05 0.1 - balance 48.0 3.45 Alloy 3 0.009 0.65 0.10 12.5 23.6 0.01 0.008 0.009 0.84 0.04 0.1 - balance 42.98 1.11 Alloy acc.t 0.017 0.63 0.0816.2 15.6 - 0.006 0.0090.45 - - 3.7 balance prototype
6 Table 2 - Results of determining plastic properties by bending at an angle of 90 degrees accord-ing to GOST 14019-2003 Exposure temperature, C
Alloy 550 C 625 C
Samples bending Exposure Exposure time, h . Sample bending result result Time, h Alloy acc.to pro- 720 Sample broken 720 Sample broken totype 1000 No cracks 1000 Crack 2065 Crack 2065 Crack 720 No cracks 720 No cracks Alloy 1 1000 No cracks 1000 No cracks 2065 No cracks 2065 No cracks 720 No cracks 720 No cracks Alloy 2 1000 No cracks 1000 No cracks 2065 No cracks 2065 No cracks 720 No cracks 720 No cracks Alloy 3 1000 No cracks 1000 Crack 2065 Crack 2065 Crack Table 3 - Results of industrial corrosion cracking resistance tests of alloys in chloride melts KCI, A1C13 + (ZrC14 HfC14), 100 h, at T = 650 C
Visual inspection Alloy Cracks after Corrosion rate, mm/year testing Crack in sample Pit corrosion in a sam-Alloy acc.to prototype 0.50 pie up to 0.1-0.2 mm deep No cracks Pit corrosion Alloy 1 in metal sample up to 0.16 0.1-0.2 mm deep No cracks Pit corrosion Alloy 2 in a sample up to 0.1- 0.21 0.2 mm deep Crack in sample Pit corrosion in a sam-Alloy 3 0.45 pie up to 0.1-0.2 mm deep
Alloy 550 C 625 C
Samples bending Exposure Exposure time, h . Sample bending result result Time, h Alloy acc.to pro- 720 Sample broken 720 Sample broken totype 1000 No cracks 1000 Crack 2065 Crack 2065 Crack 720 No cracks 720 No cracks Alloy 1 1000 No cracks 1000 No cracks 2065 No cracks 2065 No cracks 720 No cracks 720 No cracks Alloy 2 1000 No cracks 1000 No cracks 2065 No cracks 2065 No cracks 720 No cracks 720 No cracks Alloy 3 1000 No cracks 1000 Crack 2065 Crack 2065 Crack Table 3 - Results of industrial corrosion cracking resistance tests of alloys in chloride melts KCI, A1C13 + (ZrC14 HfC14), 100 h, at T = 650 C
Visual inspection Alloy Cracks after Corrosion rate, mm/year testing Crack in sample Pit corrosion in a sam-Alloy acc.to prototype 0.50 pie up to 0.1-0.2 mm deep No cracks Pit corrosion Alloy 1 in metal sample up to 0.16 0.1-0.2 mm deep No cracks Pit corrosion Alloy 2 in a sample up to 0.1- 0.21 0.2 mm deep Crack in sample Pit corrosion in a sam-Alloy 3 0.45 pie up to 0.1-0.2 mm deep
7
Claims (4)
1. A corrosion-resistant nickel-based alloy containing carbon, silicon, manganese, chromium, molybdenum, phosphorus, sulphur, iron, nickel and unavoidable impurities, wherein it additionally contains titanium, aluminium, niobium, magnesium with the following components ratio, wt.% :
Carbon <0.006 Silicon <0.1 Manganese <1.0 Chromium 22.8-24.0 Iron <0.75 Molybdenum 12.0-14.0 Niobium 0.01-0.03 Titanium 0.01-0.06 Aluminium 0.1-0.2 Magnesium 0.005-0.01 Phosphorus <0.015 Sulphur <0.012 Nickel and unavoidable impurities balance.
Carbon <0.006 Silicon <0.1 Manganese <1.0 Chromium 22.8-24.0 Iron <0.75 Molybdenum 12.0-14.0 Niobium 0.01-0.03 Titanium 0.01-0.06 Aluminium 0.1-0.2 Magnesium 0.005-0.01 Phosphorus <0.015 Sulphur <0.012 Nickel and unavoidable impurities balance.
2. The alloy according to claim 1, wherein the content of chromium, molybdenum and iron is related by the ratio:
[Cr] + [Mo]
> 46,4.
[Fe]
[Cr] + [Mo]
> 46,4.
[Fe]
3. The alloy according to claim 1, wherein the content of niobium and carbon is related by the ratio:
[Nb] 1, 66 [C]
[Nb] 1, 66 [C]
4. The alloy according to claim 1, wherein the content of chromium, molybdenum and iron is related by the ratio:
[Cr] + [Mo]
> 46,4 [Fe]
and the content of niobium and carbon is related by the ratio:
[NI)] > 1, 66 [C]
Date Reçue/Date Received 2022-08-12
[Cr] + [Mo]
> 46,4 [Fe]
and the content of niobium and carbon is related by the ratio:
[NI)] > 1, 66 [C]
Date Reçue/Date Received 2022-08-12
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
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RU2017127607A RU2672647C1 (en) | 2017-08-01 | 2017-08-01 | Corrosive-resistant alloy |
RU2017127607 | 2017-08-01 | ||
PCT/RU2017/001014 WO2019027347A1 (en) | 2017-08-01 | 2017-12-29 | Corrosion-resistant alloy |
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CA3093022A1 CA3093022A1 (en) | 2019-02-07 |
CA3093022C true CA3093022C (en) | 2023-08-08 |
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CA3093022A Active CA3093022C (en) | 2017-08-01 | 2017-12-29 | Corrosion resistant alloy |
Country Status (11)
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US (1) | US20210164075A1 (en) |
EP (1) | EP3663422A4 (en) |
JP (1) | JP6974507B2 (en) |
KR (1) | KR20200060694A (en) |
CN (1) | CN111094603B (en) |
CA (1) | CA3093022C (en) |
EA (1) | EA201992733A1 (en) |
JO (1) | JOP20190301A1 (en) |
MY (1) | MY192470A (en) |
RU (1) | RU2672647C1 (en) |
WO (1) | WO2019027347A1 (en) |
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IL82587A0 (en) * | 1986-05-27 | 1987-11-30 | Carpenter Technology Corp | Nickel-base alloy and method for preparation thereof |
DE3806799A1 (en) * | 1988-03-03 | 1989-09-14 | Vdm Nickel Tech | NICKEL CHROME MOLYBDENUM ALLOY |
JPH028337A (en) * | 1988-06-24 | 1990-01-11 | Nippon Stainless Steel Co Ltd | Electrifying roll for electroplating and its manufacture |
JPH05255784A (en) * | 1992-03-11 | 1993-10-05 | Sumitomo Metal Ind Ltd | Ni-base alloy for oil well excellent in corrosion resistance |
JPH0617173A (en) * | 1992-07-03 | 1994-01-25 | Mitsubishi Steel Mfg Co Ltd | Conductive roll for electroplating |
JP3485980B2 (en) * | 1994-10-03 | 2004-01-13 | Jfeスチール株式会社 | Method for producing welded clad steel pipe for boiler |
DE19723491C1 (en) * | 1997-06-05 | 1998-12-03 | Krupp Vdm Gmbh | Use of a nickel-chromium-molybdenum alloy |
US6860948B1 (en) * | 2003-09-05 | 2005-03-01 | Haynes International, Inc. | Age-hardenable, corrosion resistant Ni—Cr—Mo alloys |
US6544362B2 (en) * | 2001-06-28 | 2003-04-08 | Haynes International, Inc. | Two step aging treatment for Ni-Cr-Mo alloys |
KR20030003017A (en) * | 2001-06-28 | 2003-01-09 | 하이네스인터내셔널인코포레이티드 | TWO STEP AGING TREATMENT FOR Ni-Cr-Mo ALLOYS |
DE10302989B4 (en) * | 2003-01-25 | 2005-03-03 | Schmidt + Clemens Gmbh & Co. Kg | Use of a heat and corrosion resistant nickel-chromium steel alloy |
JP4519520B2 (en) * | 2003-09-24 | 2010-08-04 | 新日鐵住金ステンレス株式会社 | High Ni-base alloy welding wire |
JP4475429B2 (en) * | 2004-06-30 | 2010-06-09 | 住友金属工業株式会社 | Ni-base alloy tube and method for manufacturing the same |
RU2440876C1 (en) * | 2010-08-23 | 2012-01-27 | Евгений Григорьевич Старченко | Welding wire for welding structural parts from diverse steels |
JP6259336B2 (en) * | 2014-03-26 | 2018-01-10 | 日本冶金工業株式会社 | Ni-based alloy and method for producing the same |
JP6323188B2 (en) * | 2014-06-11 | 2018-05-16 | 新日鐵住金株式会社 | Manufacturing method of Ni-base heat-resistant alloy welded joint |
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2017
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- 2017-12-29 JP JP2019572506A patent/JP6974507B2/en active Active
- 2017-12-29 CN CN201780092598.3A patent/CN111094603B/en active Active
- 2017-12-29 EP EP17919968.2A patent/EP3663422A4/en not_active Withdrawn
- 2017-12-29 US US16/627,736 patent/US20210164075A1/en not_active Abandoned
- 2017-12-29 KR KR1020197038839A patent/KR20200060694A/en not_active Application Discontinuation
- 2017-12-29 EA EA201992733A patent/EA201992733A1/en unknown
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EP3663422A1 (en) | 2020-06-10 |
CN111094603B (en) | 2021-12-07 |
KR20200060694A (en) | 2020-06-01 |
BR112019028257A2 (en) | 2020-08-04 |
EA201992733A1 (en) | 2021-04-20 |
WO2019027347A1 (en) | 2019-02-07 |
JOP20190301A1 (en) | 2019-12-30 |
RU2672647C1 (en) | 2018-11-16 |
CN111094603A (en) | 2020-05-01 |
WO2019027347A8 (en) | 2020-09-10 |
JP2020530064A (en) | 2020-10-15 |
JP6974507B2 (en) | 2021-12-01 |
US20210164075A1 (en) | 2021-06-03 |
MY192470A (en) | 2022-08-22 |
EP3663422A4 (en) | 2021-01-20 |
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