GB2039950A - Hard alloys - Google Patents
Hard alloys Download PDFInfo
- Publication number
- GB2039950A GB2039950A GB8000239A GB8000239A GB2039950A GB 2039950 A GB2039950 A GB 2039950A GB 8000239 A GB8000239 A GB 8000239A GB 8000239 A GB8000239 A GB 8000239A GB 2039950 A GB2039950 A GB 2039950A
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- United Kingdom
- Prior art keywords
- alloy
- weight
- alloys
- carbon
- chromium
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Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B23—MACHINE TOOLS; METAL-WORKING NOT OTHERWISE PROVIDED FOR
- B23K—SOLDERING OR UNSOLDERING; WELDING; CLADDING OR PLATING BY SOLDERING OR WELDING; CUTTING BY APPLYING HEAT LOCALLY, e.g. FLAME CUTTING; WORKING BY LASER BEAM
- B23K35/00—Rods, electrodes, materials, or media, for use in soldering, welding, or cutting
- B23K35/22—Rods, electrodes, materials, or media, for use in soldering, welding, or cutting characterised by the composition or nature of the material
- B23K35/24—Selection of soldering or welding materials proper
- B23K35/30—Selection of soldering or welding materials proper with the principal constituent melting at less than 1550 degrees C
- B23K35/3033—Ni as the principal constituent
- B23K35/304—Ni as the principal constituent with Cr as the next major constituent
-
- 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
- C22C19/052—Alloys based on nickel or cobalt based on nickel with chromium and Mo or W with the maximum Cr content being at least 40%
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Materials Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Manufacture And Refinement Of Metals (AREA)
Abstract
A hard, wear resistant nickel based alloy including a carbide-former, preferably niobium, and essentially cobalt free but which has similar properties to cobalt, chromium, tungsten, carbon alloys is disclosed. The alloys of the invention are suitable for surface or welding consumables, and as articles for making hardfacing depositions, and have a compositional range:- wt% Cr 26-40 one or W both Mo 6-15 C 0.55 - 2.5 one or Nb more Ti of V 1 - 7.5 Ta Hf Zr Ni Balance (at least 35%) Optionally one or both Si and Mn may be present up to 5%, Cu may be present up to 5%, aluminium and/or one of the rare earths up to 2%, B up to 1% and iron up to 25%.
Description
SPECIFICATION
Alloys
This invention relates to hard alloys and surfacing and welding consumables. In particular, it relates to nickel-based hard alloys which are resistant to wear and corrosion.
Nickel-based alloys are widely available commercially. Some of the most common of nickel-based alloys are the so-called "super alloys" which are normally strengthened by the intermetallic, gamma-prime phase.
These alloys are not resistant to wear to the same degree as for example, alloys sold under the Registered
Trade Mark Stellite.
Another well known group of nickel-based alloys are those which contain silicon and boron and sometimes chromium. These are hardened by precipitates containing boron. However, they are brittle and thus of limited use under cyclic loading conditions.
It has been proposed to formulate nickel-based alloys containing chromium, carbon and molybdenum or tungsten in an attempt to produce a general purpose, wear-resistant alloy. Such attempts have centred around producing an alloy which contains relatively high levels of carbon. As a consequence of high carbon level, these attempts have lead to an alloy whose toughness and tensile strength are limited.
Hard metal alloys, based on cobalt, are well known. Typically, they contain tungsten;chromium and carbon in addition to the cobalt. A range of such alloys is commercially available under the registered Trade
Mark 'Stellite'. In this range of alloys, the proportions of chromium and tungsten increase with increasing carbon.
There is also a need for hard, wear-resistant alloys which are cobalt free. Such alloys are especially useful in nuclear engineering where the presence of cobalt is undesirable because of its particular radioactive half-life. By hard it is meant that the alloy has a hardness greater than approximately 300 VPN.
Accordingly, the present invention provides a nickel-based hard alloy having essentially the following composition (excluding impurities) or a surfacing or welding consumable whose formulation is such that on being melted it is capable of producing an alloy which (ignoring the effect of any dilution thereof by substrate material) has essentially the following composition (excluding impurities)::
% by weight
of composition (a) Chromium 26 to 40 (b) or both of molybdenum
and tungsten 6to 15 (c) carbon 0.55 to 2.5 (d) one or more of niobium,
titanium, vanadium
tantalum, hafnium and
zirconium 1 to 7.5 (e) or both of silicon
and manganese 0two5 (f) copper O to 5 (g) aluminium 0two2 (h) one or more rare earths 0 to 2 (i) boron Oto 1 (j) iron O to 25 (k) nickel balance wherein
(1) there is at least 35% by weight of nickel in the composition.
(2) the combined weight of boron (if present) and carbon is 2.5% or less.
(3) one or more ofvandium, tantalum, hafnium and zirconium are present only when the carbon content exceeds 1.0%.
Alloys made in accordance with the present invention have properties approaching those of conventional cobalt-based alloys (Co-Cr-W-C) sold under the registered Trade Mark Stellite. The selection of any particular alloy in accordance with the composition may be made so as to meet specific requirements (such as a specified hardness).
Chromium, molybdenum and tungsten act as carbide formers and also help to strengthen the solid solution in an alloy according to the invention. Chromium and one or both of molybdenum and tungsten are
present in relatively high proportions compared with conventional nickel based hard facing alloys. The
presence of chromium and one or both of tungsten and molybdenum in such relatively high proportions is
one characteristic feature of alloys according to the invention.
Another characteristic feature of alloys according to the present invention is that they contain niobium
and/or one or more of vanadium, tantalum, titanium, hafnium and zirconium. These metals are highly active carbide formers which modify the type and morphology of the carbides and release more molybdenum (and/or tungsten) and chromium to the solid solution. The highly active carbide makes possible the formation of a hard alloy based on nickel with cobalt being absent (apart from its presence as an adventitious impurity) and without carbon being present in such high proportions that the allov is rendered unduly brittle.
When the carboncontent is 1% or less the chosen carbide former is niobium or, less preferably, titanium.
The presence of niobium or titanium allows age hardening of low carbon (1% or less) alloys through the formation of Ni3Nb and Ni3Ti.
One or both of silicon and manganese may be present. These constituents increase the fluidity of the alloys when molten.
If desired, alloys according to the invention may contain up to 5% by weight of copper which enhances their resistance to certain corrosive media. They may also include up to 2% by weight of aluminium which allows formation of the gamma prime phase in the solid solution particularly if titanium is also present.
Alloys according to the invention may also contain up to 2% by weight of one or more rare earths. The inclusion of rare earths such as lanthanum or preferably Yttrium may be desirable if an alloy according to the invention is required to have enhanced resistance to oxidation at very high temperatures. For a general purpose alloy, it is generally desirable not to employ more than 7.5% by weight of constitutents (e) to (i) inclusive.
An alloy according to the invention preferably contains from 42 to 52% by weight of nickel.
An alloy according to the invention preferably contains from 30 to 37% by weight of chromium.
Preferably, the alloys according to the invention contain no boron. If boron is present, it does not constitute more than 1% to the total weight of the alloy. Preferably the minimum carbon level is 0.9% by weight and the maximum carbon level 1.5% by weight.
An alloy according to the invention preferably contains from 1 to 4% by weight of the highly active carbide former such as niobium which is particularly preferred since it can not only form carbides but also the intermetallic compound Ni3Nb.
Iron may be present at a level up to 25% but preferably at a level not in excess of 5% by weight.
A preferred alloy according to the present invention may conform to the following composition (excluding impurities):
% by weight
Ni 42 - 52
Cr 30 - 37
One or both of Mo and W 8-12
C 0.9 - 2
Fe 0-5
One or more preferential carbide formers 1-4
Si 0-2.
Up to 2% by weight of manganese may be added to this composition if desired, in place of some or all of the silicon.
An example of an alloy according to the invention is as follows (impurities excluded).
% by weight
Cr 34
C 1.2
Mo 10
Fe 3
Si 1
Nb . 3
Ni balance
This alloy has an as cast hardness of 380 VPN, (Vickers PYRAMID No.) an ultimate tensile strength of 38 tons force per square inch, (59 H Bar), and a percentage elongation of 1%. Such an alloy may be used as a general purpose wear-resistant alloy.
In alloy of the present invention, analogously to the Stellite alloys, the more carbon that is employed, the greater is the proportion of chromium that should preferably be present. In addition, the greater the proportion of carbon, preferably, the greater is the proportion of highly active carbide former and/or the greater is the proportion of molybdenum and/or tungsten. Preferably also unless there is 1% by weight or less of carbon there is at least 32% by weight of chromium. Even if there is 1% by weight, or less of carbon there may still with advantage be 32% or more by weight of chromium.
The alloys according to the present invention may be prepared by mixing their respective ingredients and melting the resultant mixture, for example in a furnace, at a temperature in the order of 1550 C. The melting may take place in a protective atmosphere of inert gas such as argon or nitrogen or under vacuum. The molten alloy may be formed into a powder by being atomised or by other means, may be made as a casting, by, for example being poured into an appropriately shaped mould or may be formed into a wire or rod. The powder wire or rod may be formed into a cored wire or rod. The powder, wire or rod may be used as hard facing or welding consumables which may be coated with a suitable flux. It may also be possible to make forgings from alloys according to the invention, if their carbon content is less than 1% by weight.
Engineering or other components may be made as a casting or forging from an alloy of the invention, or they may be formed by compacting and or sintering a corresponding powder.
Alloys of the invention may be employed in substantially all applications for which conventional cobalt-based wear-resistant alloys are currently used.
They may, for example, be employed in the hard facing of engine valves, steam control valves and flow control valves for use in the chemicals industry. They are of particular use in the nuclear industry as they contain no cobalt (apart from that present as an impurity).
A surfacing consumable according to the invention may be used to deposit a wear resistant coating on a substrate. A welding consumable according to the invention may be used to deposit wear resistant weld metal.
An alloy according to the invention may be shaped so as to provide the surfacing or welding consumable.
Materials which in use of the consumable are not intended to become an integral part of the metallic deposit may be added, for example flux and arc stabilisers. Thus a rod of alloy according to the invention may be coated with flux and/or arc stabilisers to form a welding or surfacing consumable according to the invention.
It is possible to produce what is in effect a chemical equivalent to a welding consumable or surfacing consumable according to the invention. In such an equivalent consumable the alloy is in effect formed in situ as a metallic deposit from the consumable. This metallic deposit may be diluted almost instantaneously by the base or substrate material diffusing into or intermixing with the deposit, or vice versa. For example, some but not all constituents of the metallic deposit may be present in one discrete part of the consumable and others in another part. Thus, for example, iron may be present in an alloy forming a hollow tube, and say, nickel, molybdenum, chromium, silicon, and carbon as a powder within the tube. The tube may also typically contain a flux and arc stabilising material.
The kind of consumable in which some but not all constitutents are present in one discrete part of the consumable and others in another part may take the form of a cored wire. In such a consumable there will be near to 100% recovery of all the constitutents of the consumable in the deposit excluding arc stabilisers, flux and the like, and also with the exception that not all the silicon and/or manganese will in general be recovered, particularly if the consumable contains a flux, in which instance, in use, a part of the silicon and/or manganese tends to enter the slag which forms on the surface of the metallic deposit. Such consumables may therefore contain 1 to 2% by weight more silicon and/or manganese that it is intended to recover in the deposit.
The term "impurities" as used herein encompasses both adventitious impurities and any element or substrate deliberately added which does not significantly influence the properties of an alloy according to the invention.
Desirably, relatively pure constitutents are employed in making an alloy according to the invention.
Examples of alloys according to the invention are set out in Table 1 and their properties in Table 2.
TABLE 1
Alloy
Ref.
No. C Ni Fe Cr W Mo Si Mn Nb V Ti Ta Zr B Cu Y Al 1 1.2 Bal 3.9 33.6 8.7 1.2 3.0 2 1.29 Bal 3.0 34.0 8.9 0.9 3.0 3 1.11 Bal 3.5 33.7 9.1 1.0 3* 4 1.03 Bal 3.5 34.2 11.8 1.1 3* 5 1.09 Bal 4.5 34.5 8.2 1.9 3* 6 1.05 Bal 4.0 33.4 9.0 1.0 2.6 3* 7 1.11 Bal 3.6 26.6 9.0 1.3 3.1 1* 8 1.03 Bal 4.2 33.8 10.3 1.3 1* 1Q 9 1.67 Bal 4.5 34.7 9.0 0.8 3.0 10 2.04 Bal 6.8 35.4 11.3 1.5 5* 11 2.22 Bal 4.4 35.6 15.0 0.8 1.9 12 0.82 Bal 2.6 33.4 11.6 0.4 2.7 13 1.06 Bal 8.6 33.0 11.7 0.5 2.8 14 1.02 Bal 2.9 33.4 11.4 2* 2.6 15 0.58 Bal 2.7 33.1 11.9 1.2 1.88 0.5 * Nominal content
TABLE 2
Alloy Hardness ref. UTS2 UTS % Corrosion Oxidation
No.VPN1 Tonf/in2 H Bar Elongation (%wt.loss) (%wt gain) 1 381 38 59 1.0 1.6 0.031 2 370 0.052 3 350 35 54 0.5 0.3 0.038 4 340 43 66 1.5 0.2 0.016 5 316 31 48 0.5 4.7 0.019 6 362 47 73 1.0 0.4 7 333 44 68 1.0 5.8 0.036 8 343 41 63 0.5 0.1 0.017 9 409 21 32 0.5 4.7 0.031 10 475 23 36 0.5 2.8 0.023 11 471 20 31 0.5 12 307 42 65 2.0 0.0 0.025 13 360 43 66 1.0 2.1 0.022 14 332 45 69 1.0 0.5 0.020 15 338 43 66 1.0 1.9 0.014 1. Vickers Pyramid Number 2. Ultimate Tensile strength
The methods used in the determination of the physical properties were as follows.
Room Temperature hardness
Room temperature hardness of each alloy was determined using a standard Vickers hardness tester (obtainable from Vickers Limited). Indentations were formed in a parallel sided specimen (precision cast and polished on one face by successive use of silicon carbide paper and diamond polishing wheels) under a load of 30kg. The result quoted is an average of five readings.
Ultimate Tensile strength (UTSJ and elongation
Tensile testing of the alloys was carried out using a Hounsfield Tensometer (available from Monsanto
Limited) and test pieces precision cast to the dimensions specified in British Standard 18, described in
Methods for Tensile testing of metals published by the British Standards Institute. For each alloy test pieces were first X-ray inspected, and three tests were performed the average ultimate tensile strength and percentage elongation being quoted.
Corrosion in Room Temperature Aqua Regia
To determine the resistance of each alloy to room temperature aqua regia, a precision cast test piece of known weight and approximate surface area 30cm2 was totally immersed in 100cm3 of aqua regia for 100 hours. After immersion, the samples were washed, brushed lightly to remove any scale, and reweighed. The weight loss, as a percentage of the original weight was used as a measure of resistance.
Oxidation in Still Air
To determine the resitance of each alloy to oxidation in still air a precision cast test piece of known weight and approximate surface area 30cm2 was placed in a muffle furnace at 9000C for 25 hours. Temperature control in the muffle furnace was to within plus or minus 2 C.
To enable spalled oxide scale to be collected and counted in the final weight gain measurement, each sample was held in a high-sided platinum dish during oxidation. The total weight gain as a percentage of the original weight was used as a measure of oxidation resistance.
As shown by Tables 1 and 2 the alloys made in accordance with the present invention have acceptable hardness and tensile properties excellent resistance to corrosion (as a result of the presence of a high level of chromium in the solid solution) and adequate oxidation resistance.
If a suitable carbide former is not present (as in alloy No. 16) to modify the carbide second phase and to release more chromium and molybdenum/tungsten to the solid solution, the tensile properties and corrosion resistance are much reduced.
A comparison of the properties of an alloy according to the present invention (No. 1) a similar carbide-former free alloy (No.16) and a Co-Cr-W-C stellite alloy (No.17) is given in Table 4. The composition of the alloys is shown in Table 3.
TABLE 3
composition by weight
Alloy
Ref
No. C Ni Co Fe Cr Mo W Si Nb 1 1.2 Bal 3.9 33.6 8.7 1.2 3.0 16 1.88 Bal 3.5 33.3 10.6 0.8 17 1.22 1.0 Bal 2.9 25.7 0.3 5.1 1.0
TABLE 4
corros- oxida
Alloy Ref Hardness UTS UTS Elong- ion% tion %
No. (VPN) Tonf/in2 H Bar ation % wt loss wt gain 1 381 38 59 1.0 1.6 0.031 16 380 23 36 0.5 9.3 0.010 17 420 54 83 1.2 6.5 0.019
Elevated temperature properties of alloys similar to No. 1 (No. 18) and comparative alloy No. 17 (No. 19) are compared in Table 6. The composition of the alloys is given in Table 5.
TABLE 5
Alloy
Ref
No. C Ni Co Fe Cr Mo W Si Nb 18 1.04 Bal - 3* 34* 10* - 0.99 3* 19 1.18 2.2 Bal 2.7 27.1 0.5 5.2 1.3 * nominal content
TABLE 6
Alloy No. 18 Alloy No. 19
Temperature UTS UTS % HARDNESS UTS UTS Elongation HARDNESS C Tonf/in2 H Bar Elongation VPN Tonf/in2 H Bar % VPN
R.T 45 69 1.0 386 54 83 1.2 366 400 37 57 0.8 43 66 2.7 500 318 297 600 38 59 1.0 38 59 2.8 700 264 264 800 33 51 3.0 33 51 7.6
The properties at elevated temperature were determined as follows:
Elevated temperature tensile properties
The elevated temperature tensile properties were determined by use of a Hounsfield Tensometer and its high temperature tensile attachments. These comprise a muffle furnace (obtained from Wild Barfield
Limited) with suitable hot zone and a set of extension rods and collets manufactured from an alloy resistant to high temperature oxidation. The temperature of the furnace hot zone was controlled to plus or minus 5"C during testing. Samples were held at the test temperature for ten minutes prior to stressing (to allow complete heating). For each alloy and temperature at least two tests are performed. The results quoted are averages.
The above results demonstrate that at temperatures of the order of 7000C an alloy made in accordance with the invention and its cobalt-based counterpart have similar hardness values and ultimate tensile strengths. These properties can be related to the ability of the alloys to resist deformation.
Claims (16)
1. A nickel-based hard alloy having essentially the following composition (excluding impurities) or a surface or welding consumable whose formulation is such that on being melted it is capable of producing an alloy which (ignoring the effect of any dilution thereof by substrate material) has essentially the following composition:
% by weight
of composition (a) chromium 26to40 (b) one or both of molybdenum
and tungsten 6to15 (c) carbon 0.55to 2.5 (d) one or more of niobium,
titanium, vanadium,
tantalum, hafnium and
zirconium 1 to 7.5 (e) one or both silicon and
manganese 0 to 5 (f) copper up to 5 (g) aluminium 0 to 2 (h) one or more rare earths 0 to 2 (i) boron 0 to 1 (j) iron 0 to 25 (k) nickel balance wherein: (1) there is at least 35% by weight of nickel in the composition.
(2) the combined weight of boron (if present) and carbon is 2.5% or less.
(3) one or more of vanadium, tantalum, hafnium and zirconium are present only when the carbon content exceeds 1.0%.
2. An alloy as claimed in claim 1 in which the composition contains from 0.4% to 2.5% by weight of one or both of silicon and manganese.
3. An alloy as claimed in claim 2 containing up to 2% by weight of silicon.
4. An alloy as claimed in claim 1 or claim 2 containing from 0.9 to 1.5% by weight of carbon.
5. An alloy as claimed in any one of claims 1 to 4 containing from 30 to 37% by weight of chromium.
6. An alloy as claimed in claim Sin which the composition contains at least 32% by weight of chromium.
7. An alloy as claimed in any one of the preceding claims, containing up to 5% by weight of iron.
8. An alloy as claimed in claim 1 in which the rare earth is yttrium.
9. An alloy as claimed in any one of the preceding claims containing from 1 to 4% by weight of one or more of niobium, vanadium, hafnium, tantalum titanium and zirconium.
10. An alloy as claimed in any one of the preceding claims, containing from 42 to 52% by weight of nickel.
11. An alloy as claimed in any one of the preceding claims in which boron is present.
12. An alloy as claimed in any one of the preceding claims, in which the composition contains 7.5% by weight or less of constituents (j) to (k).
13. An alloy as claimed in any one of the preceding claims, in which tungsten is absent.
14. An alloy as claimed in claim 2, having the following composition (excluding impurities):
% by weight
Ni 42 to 52 Cr 30 to 37 One or both of Mo and W 8to12 C 0.9to 2
Fe Oto 5
One or more of Nb, Hf, V, Ti,
TaandZr 1 to 4
Mn Oto 2
Si up to 2
15. An alloy as claimed in Claim 14, having the following composition (excluding impurities):
%by weight
Cr 34
C 1.2
Mo 10
Fe 3
Si I Nb 3
Ni balance
16. An alloy having (excluding impurities) any one of the compositions'set out in Table 1 herein.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB8000239A GB2039950B (en) | 1979-01-11 | 1980-01-04 | Hard alloys |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB7901144 | 1979-01-11 | ||
GB8000239A GB2039950B (en) | 1979-01-11 | 1980-01-04 | Hard alloys |
Publications (2)
Publication Number | Publication Date |
---|---|
GB2039950A true GB2039950A (en) | 1980-08-20 |
GB2039950B GB2039950B (en) | 1983-06-15 |
Family
ID=26270206
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB8000239A Expired GB2039950B (en) | 1979-01-11 | 1980-01-04 | Hard alloys |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB2039950B (en) |
Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0057242A1 (en) * | 1981-02-04 | 1982-08-11 | Eaton Automotive Spa. | High temperature alloy |
EP0068284A1 (en) * | 1981-06-15 | 1983-01-05 | Kabushiki Kaisha Toshiba | Wear-resistant alloy |
US4754950A (en) * | 1984-10-30 | 1988-07-05 | Kabushiki Kaisha Toshiba | Valve |
GB2205583A (en) * | 1987-05-19 | 1988-12-14 | Harbin Research Inst Of Weldin | Ni-base wear resistant alloy for hard surfacing |
GB2390855B (en) * | 2002-05-15 | 2005-10-26 | Haynes Internat Inc | Ni-Cr-Mo alloys resistant to wet process phosphoric acid and chloride-induced localized attack |
US8941032B2 (en) * | 2004-02-16 | 2015-01-27 | Kevin Francis Dolman | Hardfacing ferroalloy materials |
US20150093284A1 (en) * | 2013-09-30 | 2015-04-02 | Liburdi Engineering Limited | Welding material for welding of superalloys |
EP3137253A4 (en) * | 2014-04-28 | 2017-10-04 | Liburdi Engineering Limited | A ductile boron bearing nickel based welding material |
EP3898043A4 (en) * | 2018-12-19 | 2023-02-08 | Oerlikon Metco (US) Inc. | High-temperature low-friction cobalt-free coating system for gate valves, ball valves, stems, and seats |
-
1980
- 1980-01-04 GB GB8000239A patent/GB2039950B/en not_active Expired
Cited By (16)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0057242A1 (en) * | 1981-02-04 | 1982-08-11 | Eaton Automotive Spa. | High temperature alloy |
EP0068284A1 (en) * | 1981-06-15 | 1983-01-05 | Kabushiki Kaisha Toshiba | Wear-resistant alloy |
US4585620A (en) * | 1981-06-15 | 1986-04-29 | Tokyo Shibaura Denki Kabushiki Kaisha | Wear-resistant alloy for an atomic power plant |
US4754950A (en) * | 1984-10-30 | 1988-07-05 | Kabushiki Kaisha Toshiba | Valve |
GB2205583A (en) * | 1987-05-19 | 1988-12-14 | Harbin Research Inst Of Weldin | Ni-base wear resistant alloy for hard surfacing |
GB2205583B (en) * | 1987-05-19 | 1991-04-24 | Harbin Research Inst Of Weldin | Co-free ni-base wear resistant alloy for hard surfacing |
GB2390855B (en) * | 2002-05-15 | 2005-10-26 | Haynes Internat Inc | Ni-Cr-Mo alloys resistant to wet process phosphoric acid and chloride-induced localized attack |
US8941032B2 (en) * | 2004-02-16 | 2015-01-27 | Kevin Francis Dolman | Hardfacing ferroalloy materials |
US20150093284A1 (en) * | 2013-09-30 | 2015-04-02 | Liburdi Engineering Limited | Welding material for welding of superalloys |
CN104511702A (en) * | 2013-09-30 | 2015-04-15 | 利宝地工程有限公司 | Welding material for welding of superalloys |
EP2853339A3 (en) * | 2013-09-30 | 2015-08-12 | Liburdi Engineering Limited | Welding material for welding of superalloys |
US10414003B2 (en) * | 2013-09-30 | 2019-09-17 | Liburdi Engineering Limited | Welding material for welding of superalloys |
EP3137253A4 (en) * | 2014-04-28 | 2017-10-04 | Liburdi Engineering Limited | A ductile boron bearing nickel based welding material |
RU2666822C2 (en) * | 2014-04-28 | 2018-09-12 | Либурди Инжиниринг Лимитед | Ductile boron-bearing nickel based welding material |
EP3898043A4 (en) * | 2018-12-19 | 2023-02-08 | Oerlikon Metco (US) Inc. | High-temperature low-friction cobalt-free coating system for gate valves, ball valves, stems, and seats |
US11644106B2 (en) | 2018-12-19 | 2023-05-09 | Oerlikon Metco (Us) Inc. | High-temperature low-friction cobalt-free coating system for gate valves, ball valves, stems, and seats |
Also Published As
Publication number | Publication date |
---|---|
GB2039950B (en) | 1983-06-15 |
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