CERMET POWDER, PROTECTIVE-COATING-COATED MEMBER AND METHOD OF PRODUCING SAME, AND ELECTROPLATING-BATH-IMMERSED ROLL AND METHOD OF PRODUCING SAME

Abstract

Disclosed is a cermet powder that enables preparation of a cermet coating having both high wear resistance and high corrosion resistance against a strong acid having a pH of less than 1. The disclosed cermet powder contains tungsten carbide particles in an amount of 40 mass % or more; molybdenum carbide particles in an amount of 10 mass % to 40 mass %; and Ni or a Ni alloy as a matrix metal, wherein the cermet powder further contains chromium, either as a carbide or a metal or alloy element contained in the matrix metal, in an amount of 8 mass % or more.

Claims

1. A cermet powder containing: tungsten carbide particles in an amount of 40 mass % or more; molybdenum carbide particles in an amount of 10 mass % to 40 mass %; and Ni or a Ni alloy as a matrix metal, wherein the cermet powder further contains chromium, either as a carbide or a metal or alloy element contained in the matrix metal, in an amount of 8 mass % or more.

2. The cermet powder according to claim 1, wherein the tungsten carbide particles have a content of 70 mass % or less.

3. The cermet powder according to claim 1, wherein the tungsten carbide particles have a particle size distribution within a range of 0.1 m to 6 m.

4. The cermet powder according to claim 1, wherein the molybdenum carbide particles have a particle size distribution within a range of 0.1 m to 6 m.

5. A protective-coating-coated member comprising: a stainless steel base member; and a cermet coating formed on the stainless steel base member, wherein the cermet coating comprises a matrix made of Ni or a Ni alloy, in which tungsten carbide particles and molybdenum carbide particles are dispersed, and the cermet coating contains the tungsten carbide particles in an amount of 40 mass % or more, the molybdenum carbide particles in an amount of 10 mass % to 40 mass %, and chromium, either as a carbide or a metal or alloy element contained in the matrix, in an amount of 8 mass % or more.

6. The protective-coating-coated member according to claim 5, wherein the tungsten carbide particles have a content of 70 mass % or less.

7. The protective-coating-coated member according to claim 5, wherein the tungsten carbide particles in the cermet coating have a particle size distribution within a range of 0.1 m to 6 m.

8. The protective-coating-coated member according to claim 5, wherein the molybdenum carbide particles in the cermet coating have a particle size distribution within a range of 0.1 m to 6 m.

9. The protective-coating-coated member according to claim 5, wherein the cermet coating has a surface roughness Ra of 0.5 m to 10 m.

10. A method of producing a protective-coating-coated member, comprising thermal spraying the cermet powder as recited in claim 1 onto a stainless steel base member.

11. The method of producing a protective-coating-coated member according to claim 10, wherein the thermal spraying is HVOF thermal spraying.

12. An electroplating-bath-immersed roll comprising the protective-coating-coated member as recited in claim 5.

13. An electroplating-bath-immersed roll comprising a roll shaft portion and a roll body portion, both made of stainless steel, wherein only the roll body portion comprises the protective-coating-coated member as recited in claim 5.

14. A method of producing an electroplating-bath-immersed roll, the method comprising: preparing a roll member comprising a roll shaft portion and a roll body portion, both made of stainless steel; and forming a cermet coating only onto the roll body portion by thermal spraying the cermet powder as recited in claim 1.

15. The method of producing an electroplating-bath-immersed roll according to claim 14, wherein the thermal spraying is HVOF thermal spraying.

Description

BRIEF DESCRIPTION OF THE DRAWING

[0036] In the accompanying drawings:

[0037] FIG. 1 is a schematic cross-sectional view of a protective-coating-coated member 100 according to one of the embodiments of the present disclosure; and

[0038] FIG. 2A is a schematic cross-sectional view of a conventional electroplating-bath-immersed roll 200, while FIG. 2B is a schematic cross-sectional view of an electroplating-bath-immersed roll 300 according to one of the embodiments of the present disclosure.

DETAILED DESCRIPTION

[0039] (Cermet Powder)

[0040] A cermet powder according to one of the embodiments of the present disclosure contains: tungsten carbide particles in an amount of 40 mass % or more; molybdenum carbide particles in an amount of 10 mass % to 40 mass %; Ni or a Ni alloy as a matrix metal; and chromium either as a carbide or a metal or alloy element in the matrix, in an amount of 8 mass % or more. With this cermet powder, it is possible to produce a cermet coating that offers both high wear resistance and high corrosion resistance against a strong acid having a pH of less than 1. Each component of the cermet powder of the present disclosure will be described below.

[0041] The tungsten carbide particles serve to impart high wear resistance and relatively high corrosion resistance to the cermet coating. The tungsten carbide particles include for example WC particles. The content of the tungsten carbide particles needs to be 40 mass % or more. The reason is that if it is less than 40 mass %, the cermet coating cannot provide sufficient wear resistance. Also, the content of the tungsten carbide particles is preferably 70 mass % or less. The reason is that if it exceeds 70 mass %, the content of the other components becomes so small that the cermet coating cannot provide high corrosion resistance against a strong acid having a pH of less than 1. From the viewpoint of reliably achieving the effect of the present disclosure, the tungsten carbide particles preferably have a particle size distribution within a range of 0.1 m to 6 m.

[0042] The molybdenum carbide particles are important components in the present disclosure, which plays a role of imparting to the cermet coating not only high wear resistance but also high corrosion resistance to a strong acid having a pH of less than 1. The molybdenum carbide particles include for example Mo.sub.2C particles. The content of the molybdenum carbide particles needs to be 10 mass % to 40 mass %. The reason is that if the content is less than 10 mass %, the cermet coating cannot provide high corrosion resistance against a strong acid having a pH of less than 1, and if it exceeds 40 mass %, the content of the other components, in particular, tungsten carbide particles, must be reduced, resulting in insufficient wear resistance of the cermet coating. From the viewpoint of reliably achieving the effect of the present disclosure, the molybdenum carbide particles preferably have a particle size distribution within a range of 0.1 m to 6 m.

[0043] The cermet powder of the present disclosure contains Ni or a Ni alloy as a matrix metal. Examples of the Ni alloy include a NiCr-based alloy, a NiCrMo-based alloy, and a NiCoCrAlY-based alloy, containing Ni as a main component. Ni as a matrix metal plays a role of imparting to the cermet coating high corrosion resistance to a strong acid having a pH of less than 1. From this viewpoint, the Ni content in the cermet powder is preferably 5 mass % or more. Further, in view of the preferable content of the other components, the Ni content in the cermet powder is preferably 20 mass % or less.

[0044] The cermet powder of the present disclosure contains chromium, either as a carbide or a metal or alloy element contained in the matrix metal, in an amount of 8 mass % or more. This chromium plays a role of imparting to the cermet coating high corrosion resistance to a strong acid having a pH of less than 1, and from that viewpoint its content needs to be 8 mass % or more. In view of the preferable content of the other components, the content of chromium in the cermet powder is preferably 20 mass % or less. In the case where the cermet powder of the present disclosure contains chromium carbide particles (Cr.sub.3C.sub.2 particles), from the viewpoint of ensuring the effect of the present disclosure, the particle size distribution thereof is preferably within a range of 0.1 m to 6 m.

[0045] The cermet powder of the present disclosure preferably consists of the above components and inevitable impurities.

[0046] In the cermet powder of the present disclosure, the molybdenum content is preferably not less than the chromium content from the viewpoint of imparting to the cermet coating high corrosion resistance to a strong acid having a pH of less than 1.

[0047] Regarding the cermet powder of the present disclosure, its production method is not particularly limited, and it can be produced by a known or arbitrary method such as a melt pulverization method, a sintering pulverization method, or a granulation sintering method.

[0048] (Protective-Coating-Coated Member and Method of Producing the Same, and Electroplating-Bath-Immersed Roll and Method of Producing the Same)

[0049] Referring to FIG. 1, a protective-coating-coated member 100 according to one of the embodiments of the present disclosure comprises: a stainless steel base member 10; and a cermet coating 20 formed on the stainless steel base member. The cermet coating 20 is formed by thermal spraying the cermet powder of the present disclosure as the thermal spray material onto the stainless steel base member 10. Consequently, in the cermet coating 20, carbide particles 24 containing tungsten carbide particles and molybdenum carbide particles, and optionally chromium carbide, are dispersed in a matrix 22 made of Ni or a Ni alloy. The content and particle size distribution of the tungsten carbide particles, the content and particle size distribution of the molybdenum carbide particles, the Ni content, the chromium content, and the particle size distribution of the chromium carbide particles in the cermet coating 20 are the same as those described above in conjunction with the cermet powder 20. In addition, an electroplating-bath-immersed roll according to an embodiment of the present disclosure comprises the protective-coating-coated member 100. The protective-coating-coated member and the electroplating-bath-immersed roll thus formed according to the present disclosure can achieve both high wear resistance and high corrosion resistance against a strong acid having a pH of less than 1.

[0050] In particular, in the present embodiment, referring to FIG. 2B, it is preferable that a roll member comprising a roll shaft portion 30 and a roll body portion 32, both made of stainless steel, is prepared, and a cermet coating 34 is formed only onto the roll body portion by thermal spraying the cermet powder disclosed herein to thereby produce a electroplating-bath-immersed roll 300.

[0051] According to the present disclosure, the protective-coating-coated member of the present disclosure and the method of producing the same, and the electroplating-bath-immersed roll and the method of producing the same were completed based on our discoveries as described below.

[0052] As mentioned above, using conventional rolls, the life of the rolls and the product yield are greatly reduced in a strong-acid plating bath such as a methanesulfonic acid solution with pH<1. In order to elucidate this phenomenon and examine countermeasures, our attention was focused on the electrochemical reaction occurring in a roll in the plating solution. First, it was considered that in a conductor roll in a plating bath, unlike ordinary corrosion reaction, a substitution reaction is in progress that is composed of two main reactions, one being a corrosion reaction (anode reaction) in which Fe (or, for example, Ni in the coated layer) becomes ions in the surface and dissolves in the solution, and the other in which Sn ions in the solution undergo electrodeposition (cathode reaction). For example, when the roll component is Fe and the plating component is Sn, these reactions can be expressed as:

cathode reaction: Sn.sup.2++2e.sup..fwdarw.Sn(1)

anode reaction: Fe.fwdarw.Fe.sup.2++2e.sup.(2).

[0053] The reactions of formulas (1) and (2) are electrochemically equivalent, and the total amount of electrons (e.sup.) generated in the anode reaction is equal to the total amount of electrons consumed in the cathode reaction. On the surface of the conductor roll under such an electrochemical reaction environment, the dissolution reaction proceeds at a portion where the potential increases locally (i.e., anode), while the electrodeposition reaction proceeds at a portion where the potential lowers locally (i.e., cathode).

[0054] In the case where the corrosion potential when the roll is immersed in the solution is relatively high, the sites where these reactions take place can be regarded as being uniformly distributed in microscopic scales, and the corrosion uniformly proceeds over the entire surface. Consequently, the surface morphology can maintain an initial good state. However, under such conditions that the plating solution is a strong acid with pH<1 or the current density of plating is set excessively high, the reaction may proceed as a result of a cathode or anode reaction taking place in a locally fixed site. In such a case, the surface morphology changes greatly as described below, which may damage the plated product.

[0055] First, with respect to the deposition of plating components such as Sn resulting from the cathode reaction, the reaction tends to concentrate at the site where deposition is initially generated, causing a metal to grow. Then, the grown metal deposit grows to a certain size, then falls off due to a load of, for example, rubbing against the steel sheet, and the site where the cathode reaction concentrates shifts to another place. By repeating such a reaction, deposition of a plating metal such as Sn progresses non-uniformly on the surface, and at the same time fragments of the plating metal that fall off may damage the surface of the steel sheet as a product.

[0056] Further, when the reaction concentrates as a result of the anode reaction being fixed at a certain site, a particular element (such as Fe in the roll) constituting the site is selectively dissolved at the grain boundary or the like, which may cause the roll surface or the coated layer to partially fall off as fragments. These fragments that have fallen off from the surface may damage the surface of the steel sheet as a product.

[0057] In other words, in a conventional roll as described above, the corrosion potential relatively decreases in a strong acid plating bath with pH<1 or when the current density is excessively high, and the microscopic uniformity of the distribution of the anode and the cathode is reduced, adhesion/detachment of the plating metal and partial damage in the roll surface become conspicuous as a result of localized immobilization, and this may be the cause of decrease in the product yield.

[0058] Therefore, in order to secure the roll life and to maintain a high product yield even in a strong acid plating bath with pH<1 or even when the current density is set high for the purpose of increasing the line speed, it is necessary to find out a material that can prevent as much as possible the phenomenon in which the reaction would concentrate as a result of a cathode or anode reaction taking place in a locally-fixed site as described above, rather than focusing simply on the amount of reaction. Conversely, providing such a material can prevent the progress of local corrosion as described above, guaranteeing the life of the roll and the product yield.

[0059] In view of the above, static immersion tests were conducted on roll materials in a tin plating solution using methanesulfonic acid with pH<1, where the change of corrosion potential with time was measured and the degree of substitution reaction was evaluated. The test results revealed that when carbon steel was used as the roll material, the amount of reaction was extremely high, metallic Sn was deposited at every part of the surface, and the deposited lump of metallic Sn repeatedly grew and dropped. On the other hand, when stainless steel such as SUS 316L was used as the roll material, the amount of reaction was considerably low and metal Sn deposition was not found clearly, although a thin reaction layer was observed on the surface. In addition, the reaction layer on the surface could be easily removed by washing with water and chemical washing, and deposition of metallic Sn on the removed surface was not observed. The corrosion potentials at the time when 20 days passed after immersion were compared. As a result, it was found that stainless steel had a potential higher than that of carbon steel by 0.1 V or more, and maintained a potentially noble state.

[0060] From these results, we judged that the amount of reaction is small and immobilization of the anode and the cathode on the surface is not likely to occur even in a strong acid solution with pH<1 as long as the stainless steel has a corrosion potential of about 0.1 V higher than that of carbon steel. However, since the hardness of stainless steel is at most about HV 200, there is concern that the wear resistance to rubbing against the steel sheet is low. Accordingly, we made further investigations on the material of the coated layer for protecting stainless steel. It is necessary for the material for protecting stainless steel to have high hardness, excellent wear resistance, and good corrosion resistance in a strong acid plating bath. Although carbide cermets are promising as such a material, it is known that good properties cannot be obtained with the ones described in PTLs 1 to 4. However, we determined that these carbide cermets may be able to improve the electrochemical characteristics in a strong acid plating bath by adjusting the components, and engaged in further studies.

[0061] Specifically, samples were prepared by coating the surface of stainless steel as a base member with more than ten kinds of carbide cermet powders for thermal spraying including commercially available ones by HVOF thermal spraying, and immersion experiments were conducted using a strong acid plating solution with pH<1.0. The experimental results revealed that Ni or a NiCr-based alloy is superior for the matrix of the cermet, and when the carbide contains Mo carbide rather than WC particles alone, good corrosion resistance can be obtained. Therefore, as a result of our further investigations, we discovered that in order to obtain high corrosion resistance in a strong acid solution, it is desirable that Cr be contained as carbide or an alloy element in the matrix in an amount of 8 mass % or more and the content of Mo contained as carbide be at least equal to or more than the content of Cr. It was also found that Mo.sub.2C is preferable as the Mo carbide, and that if the content of Mo contained in the cermet is larger than the content of Cr, corrosion resistance will not be impaired, but conversely if the content of Mo is not more than half of the content of Cr, it is difficult to obtain a desired corrosion resistance.

[0062] That is, in a carbide cermet coating for protecting stainless steel from the substitution reaction as described above in a strong acid solution with pH <1 and for ensuring sufficient wear resistance against sliding operation with a steel sheet, it is desirable that carbide particles containing tungsten carbide particles and molybdenum carbide particles are dispersed in a matrix made of Ni or a Ni alloy, wherein the cermet coating contains the tungsten carbide particles in an amount of 40 mass % or more, the molybdenum carbide particles in an amount of 10 mass % to 40 mass %, and chromium either as a carbide or a metal or alloy element contained in the matrix, in an amount of 8 mass % or more. As a matrix containing Ni as a main component, good results were obtained with a NiCr-based alloy, a NiCrMo-based alloy, and a NiCoCrAlY-based alloy.

[0063] Specimens were prepared with a carbide cermet coating satisfying the above conditions being formed on stainless steel by HVOF thermal spraying to form a protective coating, and were subjected to constant-current anode/cathode polarization dissolution experiments. The experimental results demonstrated that the formation of a reaction layer was not significant and the surface morphology was still better than the stainless steel. In addition, as a result of measuring the corrosion potential, a potential higher by about 0.1 V than that of the stainless steel was obtained. The above results indicate that the uniformity of the distribution of the anode and the cathode formed on the surface of the above-described carbide cermet coating formed by HVOF thermal spraying is achieved at a finer level than that of stainless steel. It was thus found that there is almost no possibility of the steel sheet being damaged by the reaction product. In this way, we discovered that a protective layer having good corrosion resistance can be formed even in a strong acid plating bath, while having excellent wear resistance.

[0064] Here, it was determined that it is important to adjust the particle size of the tungsten carbide particles and the molybdenum carbide particles, which are the main components of the cermet, for achieving both wear resistance and corrosion resistance in a trade-off relationship. Specifically, it was found that when carbides, which are the main component of the cermet, having particle sizes of less than 0.1 m are used, the wear resistance is remarkably deteriorated, and when particles having a particle size of 6 m or more are used, the uniformity of the distribution of the anode and the cathode in the solution cannot be maintained sufficiently in microscopic scales. It was determined that when the particle size of the tungsten carbide particles and the molybdenum carbide particles is in the range of 0.1 m to 6 m, both wear resistance and corrosion resistance can be compatible.

[0065] As a method of forming a protective layer, a high-velocity flame spraying method such as HVOF or HVAF was found to be desirable. For example, when comparing the cermet coating obtained by a high-velocity flame spraying method such as HVOF or HVAF with the cermet coating by plasma spraying or other thermal spraying method, the porosity greatly differs, and in the case of a layer obtained by a thermal spraying method other than the high-velocity flame spraying method such as HVOF or HVAF, it was difficult to maintain a satisfactory surface condition; for example, the solution infiltrated into the layer. Also, when heat treatment is performed on the resulting layer at a high temperature for the purpose of lowering the porosity, the carbide is decarburized into lower carbide or a reaction phase forms with the matrix components, causing a remarkable degradation in wear resistance and corrosion resistance. Such a tendency was also seen in the layers formed by weld overlaying and cladding method. That is, a high-velocity flame spraying method such as HVOF or HVAF is preferable as the method of forming a carbide cermet coating.

[0066] It was found that even with a protective layer formed by a high-velocity flame spraying method such as HVOF or HVAF, the probability of scratching the steel sheet with protrusions of carbide increases when the surface roughness Ra exceeds 10 m, and when Ra is less than 0.5 m, the frictional force is not sufficient and the roll idly rotates on the steel sheet, resulting in impairment of the surface condition of the steel sheet. Therefore, the surface roughness Ra of the carbide cermet coating is preferably 0.5 m to 10 m.

EXAMPLES

Example 1

[0067] Samples were prepared in conformity with conventional roll specifications and roll specifications according to the present disclosure, and subjected to immersion tests for 20 days in a strong-acid plating solution (methanesulfonic acid 50 g/L, tin ion concentration 25 g/L) adjusted to pH<1. Five samples listed in Table 1 were prepared. Specifically, in Sample No. 1, the base member was a conventional carbon steel and the protective layer was also a conventional sample. On the other hand, in Sample Nos. 2 to 5, the base member was made of stainless steel. Regarding the protective layers, Sample No. 2 adopted a conventional layer as in Sample No. 1, and Sample Nos. 3 to 5 used HVOF layers of various carbide cermets using Ni or a Ni base alloy as the matrix; among these, Sample No. 5 corresponds to the cermet specification of our example of the present disclosure. In the layer of Sample No. 5, the Mo content was 9.4 mass %, the Cr content was 8.7 mass %, the WC particle size was 0.1 m minimum and 6 m maximum, the particle size of Mo.sub.2C particles was 0.1 m minimum and 6 m maximum, and the surface roughness Ra was 3.0 m. Each sample was prepared such that the exposed portion of the base member and the protective layer portion had substantially the same surface area and devised such that the properties of the boundary portion between the layer and the base member could be evaluated.

[0068] To evaluate the corrosion resistance of the protective layer, the change in mass (weight loss due to corrosion) before and after immersion was measured for each sample, and the results are presented in Table 1. In addition to the change in mass, Table 1 lists the results of observation of the surface conditions of the protective layer with the electron microscope after immersion for 20 days, as well as the measurements of the corrosion potential. Table 1 also lists the results of Suga wear tests (#120-SiC paper, load 3.25 kgf, 400 reciprocations) separately performed on the protective layers. The layer observation results were evaluated according to the following criteria: [0069] Excellent: almost no change [0070] Good: slightly changed [0071] Fair: changed [0072] Poor: significantly changed

TABLE-US-00001 TABLE 1 Coating Corrosion Change Amount Sample Base observation potential in mass of wear No. Member Coating components results (V vs. Ag/AgCl) (g) (mg) Category No. 1 SS400 46Ni11Cr2.5B2.5Si2.5Fe35WC Poor 0.7 >0.46 2 Comparative Example No. 2 SUS316L 46Ni11Cr2.5B2.5Si2.5Fe35WC Poor 0.6 0.35 2 Comparative Example No. 3 SUS316L WC-20Cr.sub.3C.sub.27Ni Fair 0.6 0.33 0.5 Comparative Example No. 4 SUS316L Cr.sub.3C.sub.260CoNiCrAlY Fair 0.5 0.34 1.5 Comparative Example No. 5 SUS316L WC-10Mo.sub.2C10Cr.sub.3C.sub.210Ni Excellent 0.4 0.26 0.5 Example

[0073] As is clear from the results in Table 1, in the plating solution with pH <1, the change in mass was significant in Sample Nos. 1 to 4 in accordance with the conventional specifications, particularly in Sample No. 1 using carbon steel as the base member, leading to deterioration in the surface morphology. Furthermore, in the specimens in accordance with the conventional specification using carbon steel as the base member, the boundary between the layer and the base member was markedly broken by corrosion. In contrast, it can be seen that not only the change in mass was small but also the surface morphology was difficult to deteriorate in those samples in which stainless steel was protected with a cermet coating. In particular, in Sample No. 5 which is an example of the present disclosure, the surface morphology was much better than the other samples. This also corresponds to the measurement result of the corrosion potential (the highest in the measurement sample), demonstrating that the uniformity of the distribution of the anode and the cathode on the surface of the coating was excellent. In addition, it can be seen that our examples were excellent also from the viewpoint of wear resistance.

Example 2

[0074] Focusing on the mix proportion of the protective layer of Sample No. 5 in Example 1, various cermet powders containing Ni or a Ni-20Cr alloy as a matrix, as well as WC particles, Cr.sub.3C.sub.2 particles, and Mo.sub.2C particles with the adjusted particle size distribution within a range of 0.1 m to 6 m, were prepared. Each obtained cermet powder was HVOF thermal sprayed onto a stainless steel to form a protective layer. The composition of the layer in each sample is presented in Table 2. Immersion tests were conducted in the same way as in Example 1, and Suga wear tests were carried out. The evaluation results are presented in Table 2.

TABLE-US-00002 TABLE 2 Evaluation results Immersion test Change in Wear test Sample Chemical composition of coating (mass %) Coating observation mass Amount of No. WC Cr.sub.3C.sub.2 Mo.sub.2C Ni Ni20Cr Mo content Cr content results (g) wear (mg) Category 1 73 20 0 7 0 0 17.3 Fair 0.33 0.5 Comparative Example 2 75 10 0 15 0 0 8.7 Fair 0.35 0.7 Comparative Example 3 75 10 0 0 15 0 11.7 Fair 0.34 0.7 Comparative Example 4 70 10 10 10 0 9.4 8.7 Good 0.26 0.5 Example 5 70 10 10 0 10 9.4 10.7 Good 0.26 0.5 Example 6 60 10 20 10 0 18.8 8.7 Good 0.25 0.7 Example 7 60 10 20 0 10 18.8 10.7 Good 0.25 0.7 Example 8 50 10 30 10 0 28.2 8.7 Excellent 0.24 0.9 Example 9 50 10 30 0 10 28.2 10.7 Excellent 0.24 0.9 Example 10 50 20 20 10 0 18.8 17.3 Excellent 0.25 1.0 Example 11 40 10 40 10 0 37.6 8.7 Excellent 0.24 1.0 Example 12 30 20 30 20 0 28.2 17.3 Excellent 0.24 1.2 Comparative Example 13 30 20 30 0 20 28.2 21.3 Excellent 0.24 1.2 Comparative Example 14 20 20 50 0 10 47.1 19.3 Excellent 0.23 1.3 Comparative Example 15 10 10 70 10 0 65.9 8.7 Excellent 0.23 1.3 Comparative Example

[0075] As is apparent from the results in Table 2, it is effective to incorporate more Mo.sub.2C particles if it is intended to improve the corrosion resistance to the plating solution, and it is effective to incorporate more WC particles for improving the wear resistance. It is found that Examples 4 to 11 of the present disclosure provided both high wear resistance and high corrosion resistance against a strong acid having a pH of less than 1.

[0076] In each sample in which the cermet powder described in Example 2 was formed into a protective layer by atmospheric plasma spraying method, the porosity was high and the adverse effect such as the deterioration of the carbide was large, and as regards the corrosion resistance and the wear resistance, it was not as good as the layer produced by HVOF thermal spraying.

Example 3

[0077] A comparison is made between a conventional product and a product according to the present disclosure when applied to a conductor roll in an electroplating line. FIGS. 2A and 2B illustrate a comparison between the structure of a conventional roll and the structure of a roll according to the present disclosure. In the conventional roll in FIG. 2A, a shaft portion was formed by shrink-fitting a carbon steel tube to a copper shaft core, and a body portion was formed by shrink-fitting a carbon steel sleeve with a protective layer formed thereon by thermal spraying to a roll body portion formed of a carbon steel tube, and these were combined to form a whole roll body. In contrast, in the present disclosure, as illustrated in FIG. 2B, it is only necessary to form a thermal sprayed coating on the roll body made of stainless steel, and it will be readily appreciated that the roll body can be extremely easily fabricated. Sample No. 6 in Example 2 was adopted as the layer specification according to the present disclosure.

[0078] Heat generation by energization of each roll was measured with a thermoviewer, and both were determined to be within the range of 0.14 C./min to 0.16 C./min, in which operability is not impaired. The composition of the plating bath was the same as in Example 1. The roll pressing pressure on the steel sheet was 0.2 MPa and the sheet passing speed was in the range of 150 m/min to 490 m/min. Each roll was used for 230 days. After completion of use, each roll was pulled up from the bath, and the surface roughness of the sheet passing portion and the amount of Sn adhesion were investigated. The results are presented in Table 3.

TABLE-US-00003 TABLE 3 Conventional product Our product Ra before use 3.0 m 3.0 m Ra after use 0.81 m 1.08 m Tin adhesion to roll surface 5.2 mass % 4.7 mass % Failure rate 2.37% 0.43%

[0079] The results in Table 3 demonstrated that the surface roughness of the sheet passing portion of each conventional roll decreased from Ra of 3.0 m before use to Ra of 0.81 m, which is nearly , whereas in each roll to which the present disclosure was applied Ra of 1.0 m or more was maintained after use, and improvement of the layer life of 30% or more was achieved compared to the conventional ones. It can also be seen that the amount of Sn adhesion was reduced by about 10% in each roll of the present disclosure as compared with the conventional ones. Both of these results indicate that the corrosion resistance to the plating solution and the wear resistance against the steel sheet can be improved in accordance with the specifications of the present disclosure. In fact, the failure rate of the product was successfully lowered to 0.43%, which is or less, in the case of using rolls of the present disclosure, while it was as high as 2.37% in the case of using conventional rolls. The reason is considered to be that due to the improvement of corrosion resistance, the damage in the layer which would be the cause of defect and the occurrence rate of coarsen fragments of the electrodeposited Sn were greatly reduced.

[0080] From the results of the same actual operation, it is also found that the use limit of rolls was up to Ra of 0.5 m in surface roughness, and that the frequency at which the product suffers scratches increased with a roll having an initial surface roughness Ra exceeding 10 m. Therefore, the surface roughness Ra of the cermet coating according to the present disclosure is preferably from 0.5 m to 10 m.

INDUSTRIAL APPLICABILITY

[0081] The cermet powder of the present disclosure can be suitably used as the material of a protective layer (cermet coating) in a protective-coating-coated member such as an electroplating-bath-immersed roll. The electroplating-bath-immersed roll of the present disclosure can be suitably used, for example, as a conductor roll or the like even in an electroplating bath of a strong acid having a pH of less than 1.

REFERENCE SIGNS LIST

[0082] 100 protective-coating-coated member [0083] 10 base member (stainless steel) [0084] 20 cermet coating [0085] 22 matrix [0086] 24 carbide particles (WC particles, Mo.sub.2C particles, and optionally Cr.sub.3C.sub.2 particles) [0087] 300 electroplating-bath-immersed roll [0088] 30 roll shaft portion [0089] 32 roll body portion [0090] 34 cermet coating (thermal sprayed coating)