US2744009A - Ni-cr hard facing alloys - Google Patents

Ni-cr hard facing alloys Download PDF

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US2744009A
US2744009A US239388A US23938851A US2744009A US 2744009 A US2744009 A US 2744009A US 239388 A US239388 A US 239388A US 23938851 A US23938851 A US 23938851A US 2744009 A US2744009 A US 2744009A
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balance
alloy
boron
carbon
chromium
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US239388A
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Jr Lloyd F Bowne
Payson Peter
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Crucible Steel Company of America
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Crucible Steel Company of America
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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
    • C22C19/051Alloys based on nickel or cobalt based on nickel with chromium and Mo or W
    • C22C19/053Alloys based on nickel or cobalt based on nickel with chromium and Mo or W with the maximum Cr content being at least 30% but less than 40%
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B23MACHINE TOOLS; METAL-WORKING NOT OTHERWISE PROVIDED FOR
    • B23KSOLDERING OR UNSOLDERING; WELDING; CLADDING OR PLATING BY SOLDERING OR WELDING; CUTTING BY APPLYING HEAT LOCALLY, e.g. FLAME CUTTING; WORKING BY LASER BEAM
    • B23K35/00Rods, electrodes, materials, or media, for use in soldering, welding, or cutting
    • B23K35/22Rods, electrodes, materials, or media, for use in soldering, welding, or cutting characterised by the composition or nature of the material
    • B23K35/24Selection of soldering or welding materials proper
    • B23K35/30Selection of soldering or welding materials proper with the principal constituent melting at less than 1550 degrees C
    • B23K35/3033Ni as the principal constituent
    • B23K35/304Ni as the principal constituent with Cr as the next major constituent

Description

United States Patent Ni-Cr FACING ALLOYS Lloyd F, Bowne, J13, Livingston, N. ,J., and Peter Payson, New York, N. Y assigiors-to Crucible ,Steel .Company if America, New York, N. Y., a corporation of New ersey No Drawing. Application July 30, 1951, Serial No. 239,388
4 Claims. (Cl. 75-171) Ibis invention pertains to nickel base alloys, utilizable pri ipally a a ha d a ng l y or in s m. and containing, to this end, a relatively high carbon content, together with relatively high chromium and boron, as .essential constituents.
It is an object of this invention to provide a low melting point, nickel base alloy of high hardness and good corrosion resistance. It is a further object of this invention to provide a corrosion resistant, hard facing alloy which does not require either of the strategic alloying elements cobalt or tungsten, although small amounts of each may be present, as noted below.
It is desirable that the melting point of the alloy be relatively low so that the hard facing deposits of the alloy on a base metal can be applied rapidly and with minimum consumption of fuel. The use of a low melting point alloy also permits deposition on relatively thin sections of a base metal with minimum distortion of the underlying section.
We provide hardness and wear resistance in our alloy by incorporating carbon, boron, and chromium in it so that chromium carbides and boron compounds are present in the cast or deposited alloy. To contain the chromium carbides and boron compounds, we use nickel as a matrix, because nickel is less expensive and more readily available than cobalt, and nickel is much more corrosion resistant than iron.
In addition to providing hard compounds, carbon and boron lower the solidus temperature of the alloy and cause a wide spread between'the solidus and liquidus temperatures of the alloy. Boron also makes the alloy selffluxing. This combination of low melting point, wide range between the solidus and liquidus temperatures, and self-fluxing property, makes it possible for the alloy of this invention to be deposited from a cast rod thereof as a series of beads, by means of an electric are, or gas welding procedure, and then to be molded into a smooth surface of desired configuration, by heating the deposit to about l9.0,0 to 2l 0 0 F., and applying pressure by means of a die. The fluxing property of 'the alloy also makes it adaptable for making deposits by spraying with a metal pra gu The alloy of the invention has, for reasons explained below, the following broad, preferred, and optimum range of composition:
1 In each case the aggregate amount of carbon and boron is at least 2.2%
One application for the alloy of this invention is the hard facing of reciprocating-engine exhaust valves. Since in this application the alloy comes in contact with the products of combustion of gasoline containing lead compounds, it is essential that the alloy of this invention be highly resistant to corrosion by molten lead compounds. As a test for such resistance we immerse our alloy in liquid lead oxide at 1675 F. and hold it immersed for a period of 1 hour, after which we clean the sample and measure it for weight loss per unit of area. As shown in Table I, we have found that relatively large amounts of silicon and boron have deleterious effects on the corrosion resistance of the alloy.
Table 1.Efiect of boron and silicon on corrosion resistance of hard facing alloy in molten lead oxide at 1675 F.
Analysis, Percent Lolss 1n 1r. Alloy gmSJS'q C Si Cr B N1 in.
. 44 25. 3 1. 3 Balance 34-. 53 46 25.6 2. 2 Balance 55-. 63 46 25. 4 3. 4 Balance 1. 4-3. 3 1. 22 26. 6 3. 2 Balance 5. 1-6. 7 48 25. 4 1. 3 Balance 48-. 50 70 25. 4 2. 2 Balance 56-. 67 52 25. 7 3. 3 Balance 5. 6-5.8 38 25.2 1.3 Balance 30-. 33 42 24. 7 2. 0 Balance 72-1. 1 29. 2 1.0 Balance 1. 0-1. 1 .36 25. 1 2. 5 Balahce 30-. 38 1. 78 24. 8 2. 7 Balance 5. 2-5. 6 3. 05 25. 9 2. 8 Balance 5. 2-5. 3
On the basis of the above results, we limit the boron content in our alloy to 2.5% maximum and the silicon content to 0.5% maximum when our alloy is to be used in applications where excellent resistance to corrosion in lead oxide is required. However, for other applications where only general resistance to corrosion is required, We may use as much as 3.5% boron and as much as 1.5% silicon in our alloy.
In respect to corrosion in lead oxide, we have found that carbon in the alloy may be varied from about 0.2% to about 2.3% without much effect, as shown in Table 2.
Table 2.Eflect of carbon on corrosion resistance of hard facing alloy in molten lead oxide at 1675 F.
Analysis, Percent Llois in r., Alloy gins/sq C Si Cr B Ni in.
. 24 26 26. 5 2. 2 Balance 18-. 19 38 48 26. 7 2. 2 Balance 35-. 36 57 29 26. 3 2. 5 Balance 30-. 40 79 22 25. 8 2. 7 Balance 33-. 34 98 42 25. 2 2. 5 Balance 30-. 46 1. 16 68 25. 4 2. 5 Balance 60-. 63 l. 38 36 25. l 2. 5 Balance 30-. 38 2. 11 16 25. 9 2. 7 Balance 42-. 81 2. 33 16 26. 3 2. 8 Balance 60-. 78
effects of chromium, copper, and iron on the corrosion resistance of the alloy in molten lead oxide are shown in Table 3.
Table 3.Efiects of chromium, copper, and iron on carrosion resistance of hard facing alloy in molten lead oxide at I675 F.
Analysis, Percent Lolsls m Alloy gash.
C Si Cr B Cu Fe Ni in.
. 16 15. 2 2. 6 Balance. 40- 46 18 19. 8 2. 6 Balance. 31- 53 .36 25.1 2. Balance. .38 24 29. 5 2.8 Balance- 28- 71 26 34. 8 2. 5 Balance- 52-1. 1 .28 25.9 2.6 Balance. .39- .54 26 25. 9 2. 5 Balance- 55- 76 24 25.8 2. 5 Balance. 66- .80 76 25.3 2. 3 Balance. 28- 67 .30 26.6 2.4 Balance. .38- .39 22 26. 0 2. 6 Balance. 505. 9 31 25. 9 2. 7 Balance. 4 0 -5. 4
On the basis of the above results, we may have from 15 .to 35% chromium in our alloy, but generally We prefer to hold the chromium content to about 27% because the higher chromium alloys are more expensive and also more difficult to weld. These results also show that we may have up to 10% copper in our alloy. Since copper is less expensive than nickel, it is a desirable addition in our alloy. However, when the amount of copper in the alloy exceeds about 10%, the alloy is diflicult to deposit satisfactorily by conventional hard-surfacing techniques.
Iron is a desirable addition to our alloy from the viewpoint of cost, first, because iron is much less expensive than nickel; and sewnd, because when the alloy contains iron, ferro-chromium may be used as the means for providing chromium to the alloy rather than the much more expensive chromium metal. However, the results in Table 3 show that the corrosion resistance of the alloy is deleteriously affected when the iron content is as high as 10%. We, therefore, limit the iron content of our alloy to about 8% when the alloy is required to withstand corrosion in lead oxide. However, for applications where only general resistance to corrosion is required we may use up to 20% iron in our alloy.
The melting point of our alloy is appreciably lowered as both the carbon and boron content increase as shown in Table 4.
Table 4.Efiect of carbon and boron on the melting point of hard facing alloy Analysis, Percent Approximate Alloy Melting o si Cr B Ni 2 1. 91 55 25. 3 0. 5 Balance. 2, 325 1. 53 87 25. 0 1. 0 Balance. 2, 250 1. 80 90 29. 2 1. 0 Balance. 2, 150 .69 .44 25. 3 1. 3 Balance. 2, 200 1. O1 .48 25. 4 1. 3 Balance. 2, 125 1. 43 44 25. 5 1. 3 Balance. 2, 125 1. 86 38 25. 2 1. 3 Balance. 2,050 24 26 26. 5 2. 2 Balance. 2, 100 38 48 26. 7 2. 2 Balance. 2, 100 61 46 25. 6 2. 2 Balance. 2, 050 1. 02 70 25. 4 2. 2 Balance. 2, 050 1. 26 42 24. 3 2. 2 Balance. 2, 000 1. 85 42 24. 7 2.0 Balance. 2, 000 57 29 26. 3 2. 5 Balance. 2, 050 98 42 25. 2 2. 5 Balance. 1, 975 1. 38 36 25. 1 2. 5 Balance. 1, 975 52 46 25. 4 3. 4 Balance. 1, 975 1. 05 52 25. 7 3. 3 Balance- 1, 975 2.33 16 26. 3 2. 8 Balance. 1, 975
On the basis of these results, we use a minimum of 0.5% carbon and a minimum of 1.3% boron in our hard facing alloy so that its melting point will be under 2150 F. Obviously, when the carbon is as low as 0.70%, the boron in the alloy would have to be about 1.5% in order to have a melting point under 2150 F. We, therefore, set a minimum of 2.2% for the sum of carbon plus boron.
Our hard facing alloy as deposited has a room temperature hardness which may be as low as Rockwell C32 or as high as C62, depending on the carbon and boron contents; the higher the sum of carbon plus boron, the higher the hardness of the alloy as deposited. This room temperature hardness is practically unaffected by heating the alloy to temperatures as high as 1600 F. The hardness of the alloy at elevated temperatures decreases with increasing temperature, but reflects the hardness at room temperature; the higher the room temperature hardness, the higher the hardness at any particular elevated temperature.
Although our alloy is used mainly in the form of cast rods for applying hard surfaces by conventional welding techniques, it may also be used in powder form and applied to the surface to be covered by spraying. Our alloy may also be used in the form of castings made by usual foundry techniques. Such castings would have high hardness, corrosion, and abrasion resistance, although they would be relatively brittle.
What we claim is:
l. A nickel base alloy containing about: 0.8 to 1.8% carbon, 1.3 to 2.5% boron, the sum of carbon and boron aggregating at least 2.2%, 20 to 27% chromium, up to 0.5% silicon, up to 5% each of copper and iron, up to 2% cobalt, up to 2% of metal of the group molybdenum and tungsten, and the balance substantially nickel, characterized in having a melting point under 2150 F., a room temperature hardness within the range of about Rockwell C 32 to 62, combined with high corrosion resistance and high hardness at elevated temperatures.
2. An alloy consisting essentially of about: 0.5 to 2.2% carbon, 1.3 to 3.5% boron, the sum of carbon and boron aggregating at least 2.2%; 15 to 35 chromium, up to 1.5 silicon, up to 10% copper, up to 20% iron, up to 2% cobalt, up to 2% of metal of the group tungsten and molybdenum, balance nickel.
3. An alloy consisting of about: 0.8 to 1.8% carbon, 1.3 to 3% boron, the sum of carbon and boron aggregating at least 2.2%, 20 to 27% chromium, up to 1% silicon, up to 10% copper, up to 8% iron, up to 2% cobalt, up to 2% of metal of the group tungsten and molybdenum, balance nickel.
4. An alloy consisting of about: 0.8 to 1.8% carbon, 1.3 to 2.5 boron, the sum of carbon and boron aggregating at least 2.2%, 20 to 27% chromium, up to 0.5% silicon, up to 5% each of copper and iron, up to 2% cobalt, up to 2% of metal of the group tungsten and molybdenum, balance nickel.
References Cited in the file of this patent UNITED STATES PATENTS 1,203,555 Brix Oct. 31, 1916 1,493,191 De Golyer May 6, 1921 2,030,342 Wissler Feb. 11, 1936 2,289,641 Fetz July 14, 1942 2,292,694 Jerabek Aug. 11, 1942 2,322,507 Cole June 22, 1943 2,458,502 Cape July 11, 1949 FOREIGN PATENTS 273,209 Canada Aug. 16, 1927 886,222 France Oct. 8, 1943 OTHER REFERENCES Woldman et al.: Engineering Alloys, 2nd edition (Revised 1945), pub. by Amer. Soc. for Metals, page 448.
Woldman et 21].: Engineering Alloys, 3d edition (Revised 1954), published by Amer. Soc. for Metals, page 489.

Claims (1)

1. A NICKEL BASE ALLOY CONTAINING ABOUT: 0.8 TO 1.8% CARBON, 1.3 TO 2.5% BORON, THE SUM OF CARBON AND BORON AGGREGATING AT LEAST 2.2%, 20 TO 27% CHROMIUM, UP TO 0.5% SILICON, UP TO 5% EACH OF COPPER AND IRON, UP TO 2% COBALT, UP TO 2% OF METAL OF THE GROUP, MOLYBDENUM AND TUNGSTEN, AND THE BALANCE SUBSTANTIALLY NICKEL, CHARACTERIZED IN HAVING A MELTING POINT UNDER 2150* F., A ROOM TEMPERATURE HARDNESS WITHIN THE RANGE OF ABOUT ROCKWELL "C" 32 TO 62, COMBINED WITH HIGH CORROSION RESISTANCE AND HIGH HARDNESS AT ELEVATED TEMPERATURES.
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Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2864696A (en) * 1956-01-31 1958-12-16 Duriron Co Nickel base alloys
US2868667A (en) * 1956-10-12 1959-01-13 Wall Colmonoy Corp Method and composition for forming a porous metallic coating
US2913511A (en) * 1955-06-29 1959-11-17 Gen Electric Fuel cell
US3073269A (en) * 1957-12-24 1963-01-15 Gen Electric Metallic brazing mixture
US4181523A (en) * 1978-10-10 1980-01-01 Bhansali Kirit J Nickel-base wear-resistant alloy
EP0007124A1 (en) * 1978-07-06 1980-01-23 Metallgesellschaft Ag Nickel-base alloy
US4188209A (en) * 1976-09-01 1980-02-12 Metallgesellschaft Aktiengesellschaft Nickel-base alloy
DE3800902A1 (en) * 1987-01-14 1988-07-28 Toyota Motor Co Ltd Corrosion-resistant alloy for surface-welding
US5149597A (en) * 1989-02-10 1992-09-22 Holko Kenneth H Wear resistant coating for metallic surfaces

Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1203555A (en) * 1914-10-17 1916-10-31 American Alloys Company Metal alloy.
US1493191A (en) * 1922-11-16 1924-05-06 Golyer Anthony G De Alloy
CA273209A (en) * 1927-08-16 The Haybes Stellite Company Metal cutting tool and alloy
US2030342A (en) * 1933-07-15 1936-02-11 Union Carbide & Carbon Corp Alloy
US2289641A (en) * 1939-05-13 1942-07-14 Driver Co Wilbur B Alloy
US2292694A (en) * 1939-08-07 1942-08-11 Lincoln Electric Co Material for hard facing metallic objects
US2322507A (en) * 1943-06-22 Method of bonding
FR886222A (en) * 1941-11-24 1943-10-08 Deutsche Edelstahlwerke Ag Solder
US2458502A (en) * 1944-06-30 1949-01-11 Coast Metals Inc Structural element for high temperature service use

Patent Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA273209A (en) * 1927-08-16 The Haybes Stellite Company Metal cutting tool and alloy
US2322507A (en) * 1943-06-22 Method of bonding
US1203555A (en) * 1914-10-17 1916-10-31 American Alloys Company Metal alloy.
US1493191A (en) * 1922-11-16 1924-05-06 Golyer Anthony G De Alloy
US2030342A (en) * 1933-07-15 1936-02-11 Union Carbide & Carbon Corp Alloy
US2289641A (en) * 1939-05-13 1942-07-14 Driver Co Wilbur B Alloy
US2292694A (en) * 1939-08-07 1942-08-11 Lincoln Electric Co Material for hard facing metallic objects
FR886222A (en) * 1941-11-24 1943-10-08 Deutsche Edelstahlwerke Ag Solder
US2458502A (en) * 1944-06-30 1949-01-11 Coast Metals Inc Structural element for high temperature service use

Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2913511A (en) * 1955-06-29 1959-11-17 Gen Electric Fuel cell
US2864696A (en) * 1956-01-31 1958-12-16 Duriron Co Nickel base alloys
US2868667A (en) * 1956-10-12 1959-01-13 Wall Colmonoy Corp Method and composition for forming a porous metallic coating
US3073269A (en) * 1957-12-24 1963-01-15 Gen Electric Metallic brazing mixture
US4188209A (en) * 1976-09-01 1980-02-12 Metallgesellschaft Aktiengesellschaft Nickel-base alloy
EP0007124A1 (en) * 1978-07-06 1980-01-23 Metallgesellschaft Ag Nickel-base alloy
US4231793A (en) * 1978-07-06 1980-11-04 Metallgesellschaft Aktiengesellschaft Nickel-base alloy
US4181523A (en) * 1978-10-10 1980-01-01 Bhansali Kirit J Nickel-base wear-resistant alloy
DE2937460A1 (en) * 1978-10-10 1980-04-24 Cabot Corp WEAR-RESISTANT NICKEL ALLOY
DE3800902A1 (en) * 1987-01-14 1988-07-28 Toyota Motor Co Ltd Corrosion-resistant alloy for surface-welding
US5149597A (en) * 1989-02-10 1992-09-22 Holko Kenneth H Wear resistant coating for metallic surfaces

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