This application is a national stage application (under 35 U.S.C. §371) of PCT/EP2007/060058, filed Sep. 21, 2007, which claims benefit of German application 10 2006 045481.2, filed Sep. 22, 2006.
The invention relates to novel powder mixtures, in particular cermet powders, for the surface coating of metal substrates by thermal spraying processes such as plasma spraying or high-velocity flame spraying (HVOF), flame spraying, electric arc spraying, laser spraying or application welding, for example the PTA process.
Such powders comprise at least one finely divided hard material powder such as WC, Cr3C2, TiC, B4C, TiCN, Mo2C, etc., and a finely divided metal or alloy matrix powder. Hard material powder and matrix powder are intensively mixed, usually in the presence of a solution of an organic binder, if appropriate with comilling, atomized, dried, sieved and subsequently heated under a hydrogen-containing atmosphere to remove the organic binder and produce a sintered bond so that relatively large agglomerates having a particle size of from 10 to 100 μm are formed.
DE-B2-1446207 discloses a flame spraying powder which contains metal carbides as hard material and from 10 to 45% of aluminum and nickel as metal.
As matrix metal powders, cobalt- and nickel-containing powders, in particular, have become established in the industry.
It is a first object of the invention to reduce the use of cobalt further since cobalt has become a raw material for which demand exceeds supply because of its widespread use.
A further object of the invention is to provide low-cobalt cermet coatings which compared to customary Co—Cr matrix alloys have comparable or increased abrasion resistance and cavitation resistance.
Another object of the invention is to increase the corrosion resistance of cermet coatings, in particular to reduce the solubility of matrix metals from the coatings.
The invention provides cermet powders containing 75-90% by weight of at least one hard material powder and from 10 to 25% by weight of one or more matrix metal powders and also up to 3% by weight of modifiers,
wherein the matrix metal powder or powders contain
The invention provides for a cermet powder comprising
wherein the matrix metal powder or powders contain
Advantageous cermet powders are powders which contain 75-90% by weight of at least one hard material powder and from 10 to 25% by weight of one or more matrix metal powders and also up to 3% by weight of modifiers, wherein the matrix metal powder or powders contain up to 38% by weight of cobalt, up to 38% by weight of nickel, up to 20% by weight of aluminum, up to 90% by weight, advantageously up to 75% by weight, of iron and from 20 to 35% by weight of chromium and the sum of the contents of iron and chromium is in the range from 25 to 95% by weight and the sum of the contents of cobalt, nickel and iron is in the range from 65 to 95% by weight, advantageously from 65 to 75% by weight.
Particularly advantageous cermet powders are powders as claimed in claim 1 containing 75-90% by weight of at least one hard material powder and from 10 to 25% by weight of one or more matrix metal powders and also up to 3% by weight of modifiers, wherein the matrix metal powder or powders contain
the sum of the contents of iron and chromium is in the range from 25 to 95% by weight and the sum of the contents of cobalt, nickel and iron is in the range from 65 to 75% by weight.
A further embodiment of the invention provides cermet powders containing 75-90% by weight of at least one hard material powder and from 10 to 25% by weight of one or more matrix metal powders and also up to 3% by weight of modifiers,
wherein the matrix metal powder or powders contain
the sum of the contents of iron and chromium is in the range from 10 to 95% by weight, advantageously from 60 to 95% by weight, and the sum of the contents of cobalt, nickel and iron is in the range from 65 to 95% by weight.
In preferred cermet powders according to the invention, the matrix metals nickel and cobalt are present in a weight ratio of at least 2:3, more preferably in a weight ratio of 1:1, particularly preferably in a weight ratio of 3:2.
Particularly preferred cermet powders according to the invention are cobalt-free. Further preferred cermet powders are cobalt- and nickel-free.
More preferred, in particular low-cobalt or cobalt-free, cermet powders according to the invention have a content of iron in the matrix metal of at least 30% by weight, with the sum of the contents of iron and chromium in the matrix powder or powders being at least 60% by weight. In such cermet powders, the matrix metal powder or powders contain
In cermet powders of the invention, in particular cobalt-free cermet powders of the invention, the ratio of the sum of the contents of chromium and aluminum to the sum of the contents of iron, nickel and chromium in parts by weight is preferably from 1:2.2 to 1:3.7, particularly preferably from 1:2.7 to 1:3.6.
A preferred composition can have from 20 to 26% by weight of chromium, from 64 to 72% by weight of iron and from 5 to 16% by weight of aluminum.
Possible hard material powders are the customary hard material constituents of cermet coatings, e.g. WC, Cr3C2, VC, TiC, B4C, TiCN, SiC, TaC, NbC, Mo2C and mixtures thereof. Preference is given to WC and Cr3C2, in particular WC.
The matrix powders can be produced in a manner known per se by atomization of metal or alloy or part alloy melts. When part alloy powders or metal powders which have not been prealloyed are used, alloying occurs during use (for example during spray application) of the cermet powders.
Preferred cobalt, nickel and/or iron part alloy matrix powders are obtained by chemical precipitation by reaction of appropriate salts with excess oxalic acid, drying and thermal treatment as described in DE 198 22 663 A1 or U.S. Pat. No. 6,554,885 B1, with chromium being mixed in as metal powder.
Possible modifiers are, in particular, steel substrate upgrading elements such as Mo, Nb, Si, W, Ta and/or V.
The matrix metal or matrix alloy powders are preferably free of further constituents apart from tolerable impurities.
The present invention also provides a cermet which has the above-described composition and also a shaped article coated with such a cermet.
To produce these cermet powders, the hard material powder or powders and the matrix powder or powders and also modifiers having, if appropriate, different average particle sizes which should, however, in each case be less than 10 μm in diameter are slurried in a manner known per se in an aqueous solution of an organic binder and homogenized by means of mix-milling in a ball mill, an attritor or a stirred vessel and the suspension is atomized in a spray dryer, with the water evaporating from the sprayed droplets. The resulting powder agglomerate is converted into a powder having an intended particle size by means of classification processes (sieving, sifting) and the organic binder of the agglomerate is released into a hydrogen-containing atmosphere by sintering at a temperature of up to about 1300° C., in particular from 1100° C. to 1300° C. The resulting sinter cake is converted back into powder having the intended particle size range by physical treatment (crushing, milling, sieving, sifting).
A cermet according to the invention can be obtained by pressing and sintering of the cermet powders described or else by thermal spraying, i.e. by means of a thermal spraying process such as high-velocity flame spraying, cold gas spraying, plasma spraying or similar processes. The present invention therefore likewise provides a process for producing a cermet or an article having the above-described composition, which comprises the steps:
The present invention therefore likewise provides a process for producing a cermet or an article having the above-described composition, which comprises the steps:
A tungsten carbide powder having a particle size of 0.9 μm determined by FSSS, a carbon content of 6.1% by weight and a content of free carbon of 0.05% by weight was used in each case.
The matrix powder 1 (table 1) of examples 1 to 5 having the composition indicated there was produced by chemical precipitation using a method analogous to example 2 of DE 198 22 663 A1. The particle size was 1.4-2.2 μm FSSS at a specific surface area determined by the BET method of 1.8-2.6 m2/g. The matrix powder 2 of examples 1 to 3 is an electrolytically produced powder having a particle size D50 of 3.1 μm (laser light scattering).
The matrix metal powder of examples 6 and 7 was obtained by atomization of an alloy melt of Fe, Cr and Al. The particle size D90 was 10.8 and 10.2 μm, respectively (laser light scattering).
About 50 kg of cermet powder composed of WC and matrix alloys of the composition shown in table 1 were introduced into an initial charge of 10 l of water containing about 1% of polyvinyl alcohol (PVA, Shin-Etsu, GP05) as binder and about 0.5% of Nalco (Deutsche Nalco GmbH) as wetting agent and homogenized by means of a ball mill, the homogenized suspension was atomized in a commercial spray dryer and the water was evaporated from the spray droplets. The agglomerated powder obtained in this way is subjected to a thermal treatment and the bond is thereby converted into a sintered bond. The sintered cake obtained in this way is converted into powder in the intended particle size range by crushing, milling, sieving and sifting. The carbon content, the average particle size determined by laser light scattering, the particle size distribution and the bulk density of the cermet powders are reported in table 1.
Coatings on building steel ST37 were produced from the powders by means of high-velocity flame spraying (HVOF system Diamond Jet Hydrid 2600).
Table 2 reports the properties of the coatings.
1)in accordance with DIN EN ISO 6507
2)in accordance with ASTM G 32
3)in accordance with ASTM G65
Number | Date | Country | Kind |
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10 2006 045 481 | Sep 2006 | DE | national |
Filing Document | Filing Date | Country | Kind | 371c Date |
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PCT/EP2007/060058 | 9/21/2007 | WO | 00 | 10/1/2009 |
Publishing Document | Publishing Date | Country | Kind |
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WO2008/034902 | 3/27/2008 | WO | A |
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Number | Date | Country | |
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20100047622 A1 | Feb 2010 | US |