JP2005120457A - Coating alloy having corrosion resistance and abrasion resistance - Google Patents

Abstract

<P>PROBLEM TO BE SOLVED: To solve the problem that frictional parts such as a liner ring of an impeller in a pump and bearings are abraded and eroded by slurry, and further cause pitting corrosion and crevice corrosion after having been used for a long period of time, because the contacting liquid is corrosive like sea water and occasionally contains a solid such as the earth and sand in itself; to provide the frictional parts having both abrasion resistance/erosion resistance and pitting corrosion resistance/crevice corrosion resistance; and to provide an optimum means for adding a desired material on a base material of the component to which the properties are demanded, by a local coating treatment. <P>SOLUTION: An alloy suitable for a padding material with corrosion resistance and abrasion resistance for coating includes Ni, and by wt.% with respect to the total weight, 23-50% Cr, 7-20% V, 1.6% or more but (0.236V%+2)% or less C, Mo in an amount of at most 40% but not less than either (11-0.1xCr %)% or (125-4xCr %)% whichever is greater, and further 90% or less Cr, V and Mo in total. <P>COPYRIGHT: (C)2005,JPO&NCIPI

Description

  The present invention relates to an alloy suitable for a cladding metal material having corrosion resistance and wear resistance, and more specifically, for example, a member such as a device or an apparatus used in a corrosive environment such as seawater or a chemical substance is corroded. The present invention relates to an alloy for preventing damage due to wear and erosion, and a method for treating a surface of a member using the alloy.

For pumps, water wheels, and other fluid machinery used in corrosive environments such as seawater and chemicals, or in environments where slurry erosion occurs due to sediment or scale, the main structural parts such as casings and impellers that come into contact with liquids As a material, stainless steel having excellent corrosion resistance and cost is often used.
However, sliding parts such as impeller liner rings and bearings are damaged by wear, and if solids such as earth and sand are mixed in the handling liquid, they are further damaged by slurry erosion. become.
In addition, the sliding surface portion of the sliding component, the attachment portion to the main body, and the like are portions that inevitably have gap portions due to the structure, and in these gap portions, the corrosive liquid that has entered the gap portions is formed. Since it is difficult to replace the liquid outside the gap, pitting corrosion is likely to occur, and crevice corrosion occurs due to battery action that occurs between the inside of the gap and the surface of the member outside the gap. Even in austenitic stainless steel that exhibits excellent corrosion resistance in flowing seawater, the occurrence of crevice corrosion is a major problem. In particular, when the pump is in a shutdown state, the phenomenon that it is difficult for the liquid in the gap to be replaced with the liquid outside the gap becomes prominent, so the sliding parts of the pump exposed to repeated shutdowns will be pitting and crevice corrosion. Due to the damage caused by it, it has to be replaced in a short period of use.

In general, for the purpose of locally imparting erosion resistance (abrasion resistance / erosion resistance), a coating process of a hard material is performed and has a lot of results. Typical materials include cobalt (Co) -based alloy stellite and nickel (Ni) -based alloy colmonoy.
However, these hard coating materials do not have crevice corrosion resistance and are used in an environment such as seawater, and when applied to a member that forms a gap, corrosion proceeds rapidly.
On the other hand, Ni-base alloys such as Inconel 625 and Hastelloy C are materials with excellent pitting corrosion resistance and crevice corrosion resistance. If these are locally covered by welding overlay, damage due to pitting corrosion or crevice corrosion will occur. Although it can be prevented, it cannot withstand abrasion and erosion because of its lower hardness than the above-mentioned hard coating material.
In order to exhibit wear resistance, erosion resistance and crevice corrosion resistance simultaneously, for example, there is a method of producing a sintered body of carbide powder and Ni-based alloy powder such as Inconel 625. Production is technically and costly difficult, and sintered bodies have not been put into practical use because of structural problems.

If the liquid to be handled is corrosive, such as seawater or chemicals, and solids such as earth and sand are mixed in the liquid, the sliding parts such as pump impeller liner rings and bearings may be worn or slurried. You will be damaged by erosion.
In addition, the sliding surface part of these sliding parts, the attachment part to the main body, and the like are parts that inevitably have a gap part due to the structure, and pitting corrosion and crevice corrosion progress when used for a long period of time.
Therefore, sliding members suitable for pumps that handle corrosive fluids such as seawater and chemicals, and that contain solids such as earth and sand, are resistant to wear and erosion, as well as pitting and crevice corrosion. It is necessary to have both sex. In addition, since these properties are required only for a part of the part, it is an optimal means to add a desired material to the base material of the part by local coating treatment.

In view of the above, the present inventors have conducted research focusing on the metal forming material in order to reliably prevent wear and erosion of the sliding member, pitting corrosion, and crevice corrosion at low cost. As a result, the following findings (a) to (f) were obtained. That is,
(a) As a material for preventing corrosion by depositing on the gap surface, it is preferable that the melting point is low (equivalent to or lower than the melting point of stainless steel) in consideration of the workability of the depositing In addition, it is necessary that the metal plating does not contain voids or impurities such as oxides. From the economical aspect, a metal having a sufficient anticorrosive effect even if the metal plating layer is thin is preferable. . Ni-based alloys are the most suitable metal materials that have these properties.
(b) With Ni alone, the pitting corrosion resistance and crevice corrosion resistance in seawater are insufficient, so by adding appropriate amounts of Cr and Mo to this, excellent pitting corrosion resistance and crevice corrosion resistance can be obtained. What you can do.
(c) As a material that is less likely to be damaged by sliding and erosion due to slurry, it needs to have a high hardness, and a cermet material in which metal and carbide are combined is desirable for coating, but it has good fluidity. In order to achieve good build-up performance and to reduce the formation of voids in the coating layer, it is not necessary to build up a mixed material of carbide and metal material, but add it to the build-up metal during build-up construction. It is optimal to deposit carbides by reaction of the constituent elements.
(d) By adding appropriate amounts of vanadium (V) and carbon (C), which have low free energy for carbide formation, to the metal cladding, the above-mentioned precipitated carbide can be stably formed during the overlaying operation, and the Cr Since some Mo precipitates as carbides, it should be possible to obtain excellent wear resistance and erosion resistance.
(e) Silicon acts as a deoxidizer and can improve the hot water flowability.
(f) Furthermore, even if a portion of Ni in the metal plating material is replaced with Fe, it does not adversely affect the pitting corrosion resistance and crevice corrosion resistance, so the addition of an appropriate amount of Fe can reduce the price of the metal plating material itself and processability Can be improved.

The present invention has been made on the basis of the above findings, and an object of the present invention is to provide an alloy suitable for a cladding metallizing material excellent in corrosion resistance and wear resistance.
Another object of the present invention is excellent in corrosion resistance, wear resistance, and slurry erosion resistance, which can be used in corrosive environments such as seawater and chemical substances, or in environments where slurry erosion occurs due to sediment and scale. It is to provide an alloy suitable for a cladding material for coating.
Another object of the present invention is to provide corrosion resistance, wear resistance and slurry erosion that can be used in corrosive environments such as seawater and chemicals, earth erosion, slurry erosion due to scale, or cavitation. An object of the present invention is to provide an alloy suitable for a cladding material having excellent cavitation properties.
Still another object of the present invention is to melt the above alloy and solidify it on the surface of another member to precipitate carbide of one or more elements selected from Cr, Mo and V in the alloy. It is providing the processing method of the member surface to make.

The alloy according to one invention of the present application, in addition to Ni, as a weight percentage with respect to the whole,
23-50% Cr,
V to 7-20%,
C includes 1.6% or more and (0.236V% + 2)% or less,
Mo up to 40% or less, containing (11-0.1xCr%)% or (125-4xCr%)%, whichever is greater,
Furthermore, it is characterized in that the total of Cr, V and Mo is 90% or less.
An alloy according to another invention of the present application, in addition to Ni, as a percentage by weight with respect to the whole,
23-50% Cr,
V to 7-20%,
Si 0.5-4.5%
C includes 1.6% or more and (0.236V% + 2)% or less,
Mo up to 40% or less, containing (11-0.1xCr%)% or (125-4xCr%)%, whichever is greater,
Furthermore, it is characterized in that the total of Cr, V and Mo is 90% or less.
An alloy according to another invention of the present application, in addition to Ni, as a percentage by weight with respect to the whole,
Fe 2.5-25%
23-50% Cr,
V to 7-20%,
Si 0.5-4.5%
C includes 1.6% or more and (0.236V% + 2)% or less,
Mo up to 40% or less, containing (11-0.1xCr%)% or (125-4xCr%)%, whichever is greater,
Furthermore, it is characterized in that the total of Fe, Cr, V, and Mo is 90% or less.
In the alloy having the above composition, carbide of one or more elements selected from Cr, Mo and V may be precipitated in the alloy by melt solidification.

  A method for treating a surface of a member according to another invention of the present application is to melt an alloy having the above composition and solidify it on the surface of another member so that carbide of one or more elements selected from Cr, Mo and V is contained in the alloy. It is characterized in that it is precipitated.

As described above, the alloy suitable for the cladding material according to the present invention includes chromium (Cr), molybdenum (Mo), vanadium (V), carbon (C), silicon (Si), and iron (Fe) as component compositions. ) And the component ratio is in the above range, the reason why the component ratio is limited to the range will be described below.
(a) Cr
The Cr component is an element imparting passivating properties, and can be strengthened by addition to Ni, and the melting point can be lowered. Further, the Cr component is a carbide forming element, and the coating layer is cured by carbide precipitation. The covering layer made of the metal brazing material according to the present invention comprises two phases of a matrix metal phase and a precipitated carbide phase, and it is the composition of the metal phase that determines the corrosion resistance. Although Cr is included in both of the above two types of phases, it is difficult to control the amount of Cr carbide produced during coating construction, so the passive state strengthening takes into account the amount consumed for carbide production. In addition, it is necessary to determine the amount of Cr necessary to contribute to lowering the melting point.
Therefore, here, the effect of improving the hardness by precipitation of carbide is assumed to be secondary, and as a result of examination from the effect of passive state strengthening and melting point lowering, the desired effect cannot be obtained if the content of Cr component is less than 23%. On the other hand, even if the content exceeds 50%, there is no significant improvement in strengthening the passive state, so the content was limited to 23 to 50%.

(b) Mo
The Mo component works extremely effectively to prevent crevice corrosion in seawater. Similarly to the Cr component, the Mo component is a carbide-forming element, and the coating layer is hardened by carbide precipitation. Therefore, in the case of this Mo component as well, the effect of improving the hardness due to carbide precipitation is secondary, and as a result of examining the effect of preventing crevice corrosion, the lower limit of the Mo component content is related to the Cr component content. When the value is less than 11-0.1 × Cr% and less than 125-4 × Cr%, the desired crevice corrosion prevention effect cannot be obtained. On the other hand, there is no significant improvement in crevice corrosion improvement even if contained over 40%, so the content is limited to 11-0.1 × Cr% or more, 125-4 × Cr% or more, 40% or less did.

(c) V
Since V is an element whose free energy for carbide formation is lower than that of Cr and Mo, the V component in the metal plating material works most effectively on hardening of the coating layer due to precipitation of carbide. However, if the content is less than 7%, a desired effect cannot be obtained in the above action. On the other hand, if the content exceeds 20%, the corrosion resistance is impaired. Limited to 7-20%.
(d) C
The C component is combined with the V component, the Cr component, and the Mo component, precipitates carbides and acts on the hardening of the coating layer, and is mainly consumed for precipitation of vanadium carbides. However, if it is 1.6% or less, a desired effect cannot be obtained in the above-mentioned coating layer curing action. On the other hand, the C content necessary for all V to form carbides is V% × 12.011 (carbon atomic weight) /50.942 (vanadium atomic weight) = 0.236 × V%. However, since C forms carbides with Cr and Mo in addition to V, a C content of 0.236 XV% is insufficient for all V to form carbides. Therefore, the C content is limited to 1.6% or more and 0.236XV + 2% or less.

(e) Si
Since the Si component has a strong affinity for oxygen, it binds to oxygen in the deposit layer and works effectively to remove oxides, and improves the hot water flowability. However, if the content is less than 0.5%, the desired effect cannot be obtained in the above action. On the other hand, even if the content exceeds 4.5%, no further significant improvement effect is seen in the action. Therefore, the content was limited to 0.5 to 4.5%.

(f) Fe
Since the Fe component has an effect of improving workability in addition to an effect of reducing the cost of the metal forming material, it is contained as required when these properties are required. In addition, when adding V to the metal forming material, V alone has a high melting point and is expensive. Therefore, V is added as ferrovanadium (FeV) in order to increase the yield of material production and practically reduce the cost. Preferably, the Fe component is also contained for this reason. However, if the content is less than 2.5%, a desired effect cannot be obtained in the above action, whereas if the content exceeds 25%, the corrosion resistance deteriorates. %.

In the process of coating these alloys, it is necessary to coat the coating by a method in which there are no fine pores that cause crevice corrosion at the boundary with the base material and inside the coating. Such coating can be performed by, for example, powder overlay welding of the powder of the material by plasma transfer arc, thermal spray coating of the powder of the material, TIG welding using the welding rod of the material, or coating arc welding. A method of overlay welding, or a self-fluxing alloy coating method in which powder of the material is sprayed or a mixture of the alloy powder and an organic binder is applied, and then the material is heated and melted. Achieved by:
The member coated with the alloy of the present invention is corrosive, such as seawater and chemicals, and has a remarkable effect as a sliding member of a pump or a water turbine that handles a single-phase or two-phase or more fluid. There are no restrictions on the location. In general, erosion is rain erosion for liquid single-phase flow, sand erosion for expected and solid two-phase flow, slurry erosion for solid and liquid two-phase flow, and for gas and liquid two-phase flow. Although classified as cavitation erosion, the alloy of the present invention exhibits excellent erosion resistance in any of these. For example, cavitation erosion can be prevented by coating the cavitation generating part in the impeller of a pump that handles a corrosive liquid, taking advantage of excellent corrosion resistance, wear resistance, and erosion.
Moreover, the member covered with the alloy of the present invention can be applied not only to a pump but also to a member that requires corrosion resistance, wear resistance, and erosion resistance simultaneously in other devices and apparatuses. For example, it is very effective when used for a member that is exposed to a high-temperature gas environment containing chlorine and sulfur components and that causes erosion due to collision of flying slag and combustion residue. In addition, it is very effective when used for a member requiring particularly corrosion resistance in a flow path such as a pump for cooling water and piping used in a thermal power plant and a nuclear power plant.
Also, in chemical plants, etc., for members that require corrosion resistance and wear resistance such as the inside of fluidized bed reactors that use highly corrosive reagents and solid catalysts, or the stirrer blades and bearings of chemical reaction layers. If used, it is very effective.

(Example 1)
The method of the present invention will be described with reference to comparative examples by way of examples.
Table 1 shows the component compositions of the present invention metal plating and the comparative metal plating, the crevice corrosion test results, and the hardness test results.
First, in preparation of a sample, after forming a powdered metal material having each component composition shown in Table 1 by an atomizing method, the powder was classified and adjusted to a particle size range of 10 to 50 μm. For each of the powders, an overlay coating sample was prepared by the following procedure.
Two layers of a 3 mm thick coating were applied to one side of a SUS304 plate 60 mm wide x 100 mm long x 10 mm thick by plasma transfer arc welding. Next, the surface layer having a thickness of 1 mm was removed by machining. As a result, the coating layer deposited on the second layer is exposed on the surface. The EPMA analysis of the surface and cross section of the coating layer that was conducted separately confirmed that there was no contamination of the base material component due to dilution in the second coating layer. It can be said that the alloy has almost the same composition.

A rectangular test piece having a size of 30 mm was taken from the overlay coating sample and subjected to a crevice corrosion test.
As shown in the front view in FIG. 1 and in the longitudinal cross-sectional view in FIG. 2, a 10 mm Teflon plate 4 is attached to the center of the coating layer side of the rectangular test piece 3 with a bolt 6 and a nut through an acrylic plate 5. The test piece 3 was clamped with 7 and the surface and periphery of the test piece 3 were covered with silicon resin 2 to obtain a test specimen.
In the test, the crevice corrosion due to the solution that has entered the fine gap between the test piece 3 and the Teflon plate 4 is examined, and the specimen is immersed in a 3% NaCl aqueous solution, and the anodic polarization behavior is measured repeatedly. I took the method. FIG. 3 shows a typical example of a repetitive anodic polarization curve. Each of A, B, and C in the figure changes the potential from the natural electrode potential to the noble direction at a predetermined speed (forward path), and after the current value reaches 6 mA, reverses the potential and changes to the base direction ( It shows the state when it was made to return. In FIG. 3, A is a state in which there is almost no change in the behavior of the forward path and the backward path, and shows excellent crevice corrosion resistance. The behavior of C is completely different between the forward path and the return path, and even if the potential is changed from noble to base, the corrosion current does not decrease, and when corrosion occurs, crevice corrosion is likely to occur because corrosion does not stop. B is an intermediate state between A and C described above.

  Therefore, for each of the samples subjected to the crevice corrosion test, it was evaluated whether each cyclic anodic polarization behavior corresponds to A, B, or C in FIG. 3 above, and the result was represented by symbols A, B, and C. It is shown in Table 1. At the same time, on the test piece after repeated anodic polarization measurement, the appearance of the coating layer surface corresponding to the gap forming part was inspected, and no crack corrosion was observed at all. Table 1 is marked with x, and the occurrence of crevice corrosion is not clear, and crevice corrosion may or may not be observed in multiple measurements. Showed. That is, in Table 1, ○ indicates that crevice corrosion resistance is excellent, x indicates that crevice corrosion resistance is poor, and △ indicates that crevice corrosion resistance may be poor. Each is shown.

A test piece was appropriately collected from the surfacing coated sample residue after collecting the above-mentioned crevice corrosion test specimen, and subjected to a hardness test. In the test, a method was used in which a cross-section of the coating layer was examined and the hardness of the intermediate portion in the thickness direction of the second layer was measured with a micro Vickers hardness tester. The measurement load was 500 g. Table 1 shows the Vickers hardness (Hv) measurement results for the various samples. In addition, Hv400kgf / mm2 is defined as the evaluation standard as the hardness necessary to show wear resistance and erosion resistance for practical use, and those with higher hardness are marked with ○ in Table 1. Also shown. That is, the ◯ mark indicates that the wear resistance and erosion resistance are excellent.
From the results shown in Table 1, the overlaying samples 1 to 28 of the metal cladding according to the present invention all show wear resistance and erosion resistance in addition to excellent crevice corrosion resistance, while the composition of the components is the present invention. It is clear that the overlay coating samples 1 to 12 of the comparative metal plating material that deviated from the range are inferior in crevice corrosion resistance or wear resistance or erosion resistance.
In addition, when the appearance of the surface of the overlay metallized sample of the present invention metallizing material was observed before machining and removing the surface layer, all showed excellent metallizing properties and a smooth metallizing surface was obtained. there were.

(Example 2)
A cylindrical member having an outer diameter of φ62 mm, an inner diameter of φ51 mm, and a length of 65 mm was produced using SUS304 of austenitic stainless steel as a raw material.
This outer peripheral surface contains 29% Cr (% by weight, the same applies below), 11% Mo, 1% Si, 16% V, 5% C, and the rest is Ni-Cr-Mo-VC consisting of Ni and inevitable impurities. The alloy powder was coated to a thickness of 1.5 mm by plasma transfer arc welding. Next, the surface layer was removed by machining to produce a cylindrical member having an outer diameter of 64.4 mm, an inner diameter of 53 mm, and a length of 63 mm.
In the above embodiment, SUS304 of austenitic stainless steel is used as the base material of the base material, but any material that can be used in seawater may be used, and the present invention does not limit the type of the base material.
In the above embodiment, the plasma transfer arc welding method is used as a coating method for the coating. However, any method that does not generate pores that cause crevice corrosion at the boundary between the coating and the base material and inside the coating is used. The method is not limited. A self-fluxing alloy coating method in which the material powder is sprayed or a mixture of the material powder and an organic binder is applied and then the material is heated and melted is also applicable. However, from the viewpoint of long-term reliability of the coating, plasma transfer arc welding and TIG welding are preferable.

  The alloy suitable for the cladding material made as described above is thermally sprayed on the surface of the base material by an arbitrary thermal spraying method to form a corrosion-resistant and wear-resistant film on the base material. Examples of the substrate on which such a film is formed include members of a rotating machine, for example, equipment that requires corrosion resistance, wear resistance, sand erosion resistance, or slurry erosion resistance. By forming an abrasion-resistant film on such a substrate, it is possible to improve the abrasion resistance of such a substrate and extend the life of a machine using such equipment.

[The invention's effect]
As described above, according to the present invention, it is possible to reliably prevent wear due to sliding, erosion against dirt and scale contamination, pitting corrosion, and crevice corrosion by simply depositing a thin plate on an arbitrary surface of the sliding component. Can be used for a long period of time, preventing damage to equipment and equipment used in corrosive environments such as seawater and chemicals. Useful effects such as becoming a box office are brought about. Furthermore, it is possible to extend the life of a fluid machine using a machine part coated with the alloy of the present invention.

It is a front view of a test body. It is a longitudinal cross-sectional view of a test body. It is a schematic diagram which shows the typical example of a repetition anodic polarization curve.

Explanation of symbols

1: Lead rod, 2: Silicon resin, 3: Test piece, 4: PTFE plate, 5: Acrylic plate, 6: Bolt, 7: Nut

Claims (5)

As a percentage by weight of Ni as a whole,
23-50% Cr,
V to 7-20%,
C includes 1.6% or more and (0.236V% + 2)% or less,
Mo up to 40% or less, containing (11-0.1xCr%)% or (125-4xCr%)%, whichever is greater,
Furthermore, a Ni—Cr—Mo—VC based alloy characterized in that the total of Cr, V and Mo is 90% or less. As a percentage by weight of Ni as a whole,
23-50% Cr,
V to 7-20%,
Si 0.5-4.5%
C includes 1.6% or more and (0.236V% + 2)% or less,
Mo up to 40% or less, containing (11-0.1xCr%)% or (125-4xCr%)%, whichever is greater,
Furthermore, a Ni—Cr—Mo—VC based alloy characterized in that the total of Cr, V and Mo is 90% or less. As a percentage by weight of Ni as a whole,
Fe 2.5-25%
23-50% Cr,
V to 7-20%,
Si 0.5-4.5%
C includes 1.6% or more and (0.236V% + 2)% or less,
Mo up to 40% or less, containing (11-0.1xCr%)% or (125-4xCr%)%, whichever is greater,
Furthermore, a Ni—Cr—Mo—VC alloy characterized in that the total of Fe, Cr, V, and Mo is 90% or less. An alloy having the composition according to any one of claims 1 to 3, wherein carbide of one or more elements selected from Cr, Mo and V is precipitated in the alloy by melt solidification. Ni-Cr-Mo-VC alloy. The alloy having the composition according to any one of claims 1 to 3 is melted and solidified on the surface of another member to precipitate carbide of one or more elements selected from Cr, Mo, and V in the alloy. A method for treating the surface of a member.

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