EP3767002A1 - Piercer plug - Google Patents
Piercer plug Download PDFInfo
- Publication number
- EP3767002A1 EP3767002A1 EP19767149.8A EP19767149A EP3767002A1 EP 3767002 A1 EP3767002 A1 EP 3767002A1 EP 19767149 A EP19767149 A EP 19767149A EP 3767002 A1 EP3767002 A1 EP 3767002A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- sprayed coating
- plug
- concentration
- oxides
- iron
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
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Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B21—MECHANICAL METAL-WORKING WITHOUT ESSENTIALLY REMOVING MATERIAL; PUNCHING METAL
- B21B—ROLLING OF METAL
- B21B25/00—Mandrels for metal tube rolling mills, e.g. mandrels of the types used in the methods covered by group B21B17/00; Accessories or auxiliary means therefor ; Construction of, or alloys for, mandrels or plugs
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/02—Ferrous alloys, e.g. steel alloys containing silicon
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/04—Ferrous alloys, e.g. steel alloys containing manganese
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/08—Ferrous alloys, e.g. steel alloys containing nickel
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/12—Ferrous alloys, e.g. steel alloys containing tungsten, tantalum, molybdenum, vanadium, or niobium
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C30/00—Coating with metallic material characterised only by the composition of the metallic material, i.e. not characterised by the coating process
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C4/00—Coating by spraying the coating material in the molten state, e.g. by flame, plasma or electric discharge
- C23C4/04—Coating by spraying the coating material in the molten state, e.g. by flame, plasma or electric discharge characterised by the coating material
- C23C4/06—Metallic material
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C4/00—Coating by spraying the coating material in the molten state, e.g. by flame, plasma or electric discharge
- C23C4/04—Coating by spraying the coating material in the molten state, e.g. by flame, plasma or electric discharge characterised by the coating material
- C23C4/10—Oxides, borides, carbides, nitrides or silicides; Mixtures thereof
- C23C4/11—Oxides
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C4/00—Coating by spraying the coating material in the molten state, e.g. by flame, plasma or electric discharge
- C23C4/12—Coating by spraying the coating material in the molten state, e.g. by flame, plasma or electric discharge characterised by the method of spraying
- C23C4/123—Spraying molten metal
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C4/00—Coating by spraying the coating material in the molten state, e.g. by flame, plasma or electric discharge
- C23C4/12—Coating by spraying the coating material in the molten state, e.g. by flame, plasma or electric discharge characterised by the method of spraying
- C23C4/129—Flame spraying
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C4/00—Coating by spraying the coating material in the molten state, e.g. by flame, plasma or electric discharge
- C23C4/12—Coating by spraying the coating material in the molten state, e.g. by flame, plasma or electric discharge characterised by the method of spraying
- C23C4/131—Wire arc spraying
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B21—MECHANICAL METAL-WORKING WITHOUT ESSENTIALLY REMOVING MATERIAL; PUNCHING METAL
- B21B—ROLLING OF METAL
- B21B19/00—Tube-rolling by rollers arranged outside the work and having their axes not perpendicular to the axis of the work
- B21B19/02—Tube-rolling by rollers arranged outside the work and having their axes not perpendicular to the axis of the work the axes of the rollers being arranged essentially diagonally to the axis of the work, e.g. "cross" tube-rolling ; Diescher mills, Stiefel disc piercers or Stiefel rotary piercers
- B21B19/04—Rolling basic material of solid, i.e. non-hollow, structure; Piercing, e.g. rotary piercing mills
Definitions
- the present invention relates to a piercer plug.
- a piercer plug for piercing and rolling to produce a seamless steel pipe is provided with a scale coating on its surface before use to ensure the thermal insulation, lubrication and seizure resistance of the surface.
- a scale coating gradually wears down during each round of piercing/rolling.
- base material i.e., plug body
- the base material may be eroded and/or seize upon the material to be processed.
- a scale coating significantly wears down during piercing of a material that is difficult to process, such as stainless steel; the coating may wear out just after several passes. Each time this occurs, heat treatment is necessary to form a scale coating once again, which requires several hours to several dozens of hours, meaning poor efficiency.
- WO 2009/057471 proposes forming a sprayed coating made from iron and oxides on the surface of the base material of the piercer plug.
- WO 2014/034376 discloses a piercer plug including a sprayed coating containing iron and iron oxides and, in addition, in mass %, 0.015 to 0.6 % C, 0.05 to 0.5 % Si, 0.1 to 1.0 % Mn, and 0 to 0.3 % Cu.
- Sprayed coatings have better adhesion with respect to base material and better wear resistance than scale coatings, and can be formed in several minutes to several dozens of minutes. As such, sprayed coatings have longer lives than scale coatings, and, even when a sprayed coating has worn out, it can be restored in a short period of time. Meanwhile, it is desirable to further increase the life of piercer plugs to increase the manufacture efficiency of seamless steel pipes. It is thus desirable to further increase the wear resistance of coatings.
- An object of the present invention is to provide a piercer plug with further increased wear resistance.
- Apiercer plug includes: a plug body; and a sprayed coating formed on a surface of the plug body.
- the sprayed coating contains an iron-based alloy and an oxide of the iron-based alloy.
- a chromium concentration determined by analyzing the sprayed coating with X-ray fluorescence analysis is 3 to 20 mass %.
- the present invention provides a piercer plug with further increased wear resistance.
- FIG. 1 is a longitudinal cross-sectional view of a piercer plug 10 according to an embodiment of the present invention.
- the piercer plug 10 includes a plug body 11 and a sprayed coating 12.
- the plug body 11 is projectile-shaped. Specifically, the plug body 11 has a circular transverse section and is shaped such that its outer diameter increases as it goes from the tip of the plug body 11 toward the rear body's end.
- the plug body 11 is formed from an iron-based alloy, for example.
- the sprayed coating 12 is provided on the surface of the plug body 11.
- the sprayed coating 12 covers the entire surface of the plug body 11 except for the rear end face of the plug body 11.
- the thickness of the sprayed coating 12 may not be constant.
- the sprayed coating 12 is preferably formed such that its portions overlying the tip 11a of the plug body 11 are thicker than those overlying the body's trunk portion 11b.
- the sprayed coating 12 contains at least an iron-based alloy and oxides thereof.
- the sprayed coating 12 may contain other compounds.
- the iron-based alloy in the sprayed coating 12 is mainly composed of iron (Fe), and also contains carbon (C), silicon (Si), manganese (Mn) and chromium (Cr), for example.
- the iron-based alloy in the sprayed coating 12 may contain only one or some of C, Si, Mn and Cr, and may contain elements other than C, Si, Mn and Cr.
- the chemical composition of the iron-based alloy in the sprayed coating 12 may not be uniform. For example, when viewed microscopically, portions containing almost no Cr and portions with high Cr contents may be present in a mixed manner.
- the oxides in the sprayed coating 12 are the oxides resulting from the iron-based alloy being oxidized.
- the oxides in the sprayed coating 12 are iron oxides and complex oxides of iron and chromium, for example.
- the iron oxides may be FeO or Fe 3 O 4 , for example.
- the complex oxides of iron and chromium may be (Fe,Cr) 3 O 4 , for example.
- the oxides in the sprayed coating 12 may contain oxides of other metals.
- the proportion of metal i.e., iron-based alloy
- the proportion of oxides in the sprayed coating 12 is preferably 25 to 80 vol%, and more preferably 35 to 65 vol%.
- portions of the coating near the plug body 11 have high proportions of metal and portions located toward the surface have higher proportions of oxides. Such a construction will further increase the adhesion with respect to the plug body 11.
- the volume ratio of oxides can be determined by observing a cross section of the sprayed coating 12 and doing calculations.
- the chromium concentration determined by analyzing the sprayed coating 12 with X-ray fluorescence analysis (hereinafter referred to as "XRF-Cr concentration") is 3 to 20 mass %.
- An XRF-Cr concentration of 3 mass % or higher provides a better wear resistance than a concentration below 3 mass %. This is presumably because the complex oxides of iron and chromium increase the hardness of the sprayed coating 12. On the other hand, an XRF-Cr concentration exceeding 20 mass % results in insufficient lubrication of the sprayed coating 12, which reduces piercing efficiency.
- the lower limit for XRF-Cr concentration is preferably 5 mass %, and more preferably 8 mass %.
- the upper limit for XRF-Cr concentration is preferably 18 mass %, and more preferably 16 mass %.
- XRF-Cr concentration can be measured in the following manner: an X-ray is directed into the sprayed coating 12 through its surface, and the resulting X-ray fluorescence is detected with a detector.
- the incident X-ray is generated by a 3 mm ⁇ spot collimator with a target of Rh and an output of 40 kV ⁇ 100 pA.
- the detector is a Si drift detector.
- the concentration of Cr is determined as a mass percentage, where the denominator is the total amount of all the elements detected.
- the numerator for XRF-Cr concentration includes both the Cr amount in the iron-based alloy and the Cr amount in the oxides.
- the iron concentration determined by analyzing the sprayed coating 12 with X-ray fluorescence analysis is 50 mass % or higher.
- the determination of iron concentration by analyzing the coating with X-ray fluorescence analysis involves the same measurement method as for XRF-Cr concentration.
- the plug body 11 is prepared.
- the plug body 11 may be any plug body known to a person skilled in the art.
- a sprayed coating 12 is formed on the plug body 11.
- the sprayed coating 12 may be formed using an arc sprayer 20, shown in FIG. 2 .
- the arc sprayer 20 includes a spraying gun 21 and a rotating base 24.
- the spraying gun 21 generates an arc at the tips of a positive-electrode wire 22 and a negative-electrode wire 23 to melt metal, which is then ejected by means of compressed air.
- the chemical composition of, and the XRF-Cr concentration in, the sprayed coating 12 may be regulated by adjusting the chemical compositions of the positive- and negative-electrode wires 22 and 23.
- the positive- and negative electrode wires 22 and 23 may have the same chemical composition or may have different chemical compositions. If wires of different chemical compositions are used, metal from the positive-electrode wire 22 and metal from the negative-electrode wire 23 mix together to form a pseudo-alloy.
- the positive- and negative-electrode wires 22 and 23 may be made of carbon steel or stainless steel, for example.
- the positive- and negative-electrode wires 22 and 23 may be made of cored wire 30, shown in FIG. 3 .
- the cored wire 30 includes an outer sheath 31 made from carbon steel and a filler 32 filling the outer sheath 31.
- the chemical composition of the metal ejected from the spraying gun 21 may be changed at will by changing the type of the filler 32.
- spraying distance The longer the distance between the tip of the spraying gun 21 and the surface of the plug body 11 (hereinafter referred to as "spraying distance"), the higher the proportion of oxides in the sprayed coating 12. This is because the oxidation of metal ejected from the tip of the spraying gun 21 progresses along the spraying distance.
- the spraying distance may be 100 to 1400 mm, for example. Further, spraying at gradually increasing spraying distances results in higher proportions of metal in portions near the plug body 11 and higher proportions of oxides in portions located toward the surface.
- the numerator for XRF-Cr concentration includes both the Cr amount in the iron-based alloy and the Cr amount in the oxides. As such, the XRF-Cr concentration does not significantly change even if the proportion of oxides in the sprayed coating 12 changes. Thus, the XRF-Cr concentration does not significantly change even when the spraying distance is changed.
- Spraying is performed while the rotating base 24 rotates the plug body 11 about its axis until the thickness of the sprayed coating 12 reaches a predetermined level.
- the thickness of the sprayed coating 12 may be 200 to 3000 ⁇ m, for example.
- the formation of the sprayed coating 12 is followed by heat treatment for diffusion purposes.
- the plug is preferably held at 600 to 1250 °C for 10 minutes or longer, for example.
- the heat-treatment temperature is more preferably 600 to 1100 °C.
- the piercer plug 10 according to an embodiment of the present invention has been described.
- the XRF-Cr concentration in the sprayed coating 12 is 3 to 20 mass %. This will increase the wear resistance of the piercer plug 10.
- the plug body 11 is projectile-shaped.
- the plug body 11 may have any shape.
- the piercer plug may be a plug body 13 with a protruding tip, as shown in FIG. 4 , with a sprayed coating 12 formed thereon, or may be a plug body 14 of a divided construction, as shown in FIG. 5 , with a sprayed coating 12 formed thereon.
- the above-described embodiments illustrate implementations where the sprayed coating 12 is formed by arc spraying.
- a method for forming the sprayed coating 12 is not limited thereto.
- the sprayed coating 12 may be formed by, for example, plasma spraying, flame spraying, highspeed flame spraying, etc.
- a model plug mainly composed of 0.15 C, 0.5 Si, 1.0 Ni, 0.5 Mn, 1.5 Mo, 3.0 W, and balance Fe was prepared and a sprayed coating was formed thereon.
- a positive-electrode wire and a negative-electrode wire were prepared by combining wires of a low-carbon steel, SUS 410 and SUS 430, and cored wires with different Cr concentrations to adjust the compound of the sprayed coating to be formed.
- the XRF-Cr concentration in the sprayed coating was analyzed by the method described in connection with the embodiment.
- the X-ray fluorescence analyzer used was DP-2000 Delta Premium from JEOL Ltd., and the analysis was performed using ALLOY PLUS alloy analysis software from JEOL Ltd.
- the Vickers hardness of the sprayed coating of each plug was measured.
- the Vickers hardness of each plug was obtained by conducting three-point measurement and determining the average of the measurements.
- Table 1 shows the relationship between XRF-Cr concentration and average hardness.
- "-" in the column for XRF-Cr concentration indicates that the XRF-Cr concentration was below the lower limit for analysis.
- [Table 1] TABLE 1 Mark XRF-Cr concentration (mass %) Vickers hardness (Hv) A - 320 B 1.04 345 C 3.03 380 D 7.85 400 E 11.52 450 F 15.53 500 G 18.11 520 H 22.30 550
- FIG. 6 shows a cross-sectional microphotograph of the sprayed coating labeled Mark A in Table 1.
- FIG. 7 shows a cross-sectional microphotograph of the sprayed coating labeled Mark C in Table 1.
- a sprayed coating containing Cr was composed of metal and oxides, similar to the sprayed coating containing no Cr ( FIG. 6 ).
- relatively bright portions represent portions made from metal
- dark-gray portions represent portions made from oxides.
- the ratio between metal and oxides was substantially the same for each of the sprayed coatings prepared for the present application, where the proportion of oxides was about 44 to 55 vol%.
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Materials Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Physics & Mathematics (AREA)
- Plasma & Fusion (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Coating By Spraying Or Casting (AREA)
- Mounting, Exchange, And Manufacturing Of Dies (AREA)
- Analysing Materials By The Use Of Radiation (AREA)
Abstract
Description
- The present invention relates to a piercer plug.
- Conventionally, a piercer plug for piercing and rolling to produce a seamless steel pipe is provided with a scale coating on its surface before use to ensure the thermal insulation, lubrication and seizure resistance of the surface.
- A scale coating gradually wears down during each round of piercing/rolling. When the scale coating wears out and base material (i.e., plug body) is exposed, the base material may be eroded and/or seize upon the material to be processed. A scale coating significantly wears down during piercing of a material that is difficult to process, such as stainless steel; the coating may wear out just after several passes. Each time this occurs, heat treatment is necessary to form a scale coating once again, which requires several hours to several dozens of hours, meaning poor efficiency.
-
WO 2009/057471 proposes forming a sprayed coating made from iron and oxides on the surface of the base material of the piercer plug.WO 2014/034376 discloses a piercer plug including a sprayed coating containing iron and iron oxides and, in addition, in mass %, 0.015 to 0.6 % C, 0.05 to 0.5 % Si, 0.1 to 1.0 % Mn, and 0 to 0.3 % Cu. - Sprayed coatings have better adhesion with respect to base material and better wear resistance than scale coatings, and can be formed in several minutes to several dozens of minutes. As such, sprayed coatings have longer lives than scale coatings, and, even when a sprayed coating has worn out, it can be restored in a short period of time. Meanwhile, it is desirable to further increase the life of piercer plugs to increase the manufacture efficiency of seamless steel pipes. It is thus desirable to further increase the wear resistance of coatings.
- An object of the present invention is to provide a piercer plug with further increased wear resistance.
- Apiercer plug according to an embodiment of the present invention includes: a plug body; and a sprayed coating formed on a surface of the plug body. The sprayed coating contains an iron-based alloy and an oxide of the iron-based alloy. A chromium concentration determined by analyzing the sprayed coating with X-ray fluorescence analysis is 3 to 20 mass %.
- The present invention provides a piercer plug with further increased wear resistance.
-
- [
FIG. 1] FIG. 1 is a longitudinal cross-sectional view of a piercer plug according to an embodiment of the present invention. - [
FIG. 2] FIG. 2 illustrates exemplary equipment used to form a sprayed coating. - [
FIG. 3] FIG. 3 is a cross-sectional view of a cored wire. - [
FIG. 4] FIG. 4 is a longitudinal cross-sectional view of a piercer plug according to another embodiment of the present invention. - [
FIG. 5] FIG. 5 is a longitudinal cross-sectional view of a piercer plug according to yet another embodiment of the present invention. - [
FIG. 6] FIG. 6 is a cross-sectional microphotograph of a sprayed coating containing no Cr. - [
FIG. 7] FIG. 7 is a cross-sectional microphotograph of a sprayed coating containing Cr. - Embodiments of the present invention will now be described in detail with reference to the drawings. The same or corresponding parts in drawings are labeled with the same characters and their description will not be repeated. The size ratios between components shown in drawings do not necessarily indicate the actual size ratios.
-
FIG. 1 is a longitudinal cross-sectional view of apiercer plug 10 according to an embodiment of the present invention. Thepiercer plug 10 includes aplug body 11 and a sprayedcoating 12. - The
plug body 11 is projectile-shaped. Specifically, theplug body 11 has a circular transverse section and is shaped such that its outer diameter increases as it goes from the tip of theplug body 11 toward the rear body's end. Theplug body 11 is formed from an iron-based alloy, for example. - The sprayed
coating 12 is provided on the surface of theplug body 11. The sprayedcoating 12 covers the entire surface of theplug body 11 except for the rear end face of theplug body 11. The thickness of the sprayedcoating 12 may not be constant. The sprayedcoating 12 is preferably formed such that its portions overlying thetip 11a of theplug body 11 are thicker than those overlying the body'strunk portion 11b. - The sprayed
coating 12 contains at least an iron-based alloy and oxides thereof. The sprayedcoating 12 may contain other compounds. - The iron-based alloy in the sprayed
coating 12 is mainly composed of iron (Fe), and also contains carbon (C), silicon (Si), manganese (Mn) and chromium (Cr), for example. The iron-based alloy in the sprayedcoating 12 may contain only one or some of C, Si, Mn and Cr, and may contain elements other than C, Si, Mn and Cr. When viewed microscopically, the chemical composition of the iron-based alloy in the sprayedcoating 12 may not be uniform. For example, when viewed microscopically, portions containing almost no Cr and portions with high Cr contents may be present in a mixed manner. - The oxides in the sprayed
coating 12 are the oxides resulting from the iron-based alloy being oxidized. Specifically, the oxides in the sprayedcoating 12 are iron oxides and complex oxides of iron and chromium, for example. The iron oxides may be FeO or Fe3O4, for example. The complex oxides of iron and chromium may be (Fe,Cr)3O4, for example. The oxides in the sprayedcoating 12 may contain oxides of other metals. - The higher the proportion of metal (i.e., iron-based alloy) that is an ingredient in the sprayed
coating 12, the better the adhesion with respect to theplug body 11. On the other hand, the higher the proportion of oxides, the better the heat insulation. Although not limiting, the proportion of oxides in the sprayedcoating 12 is preferably 25 to 80 vol%, and more preferably 35 to 65 vol%. Further, it is preferable that portions of the coating near theplug body 11 have high proportions of metal and portions located toward the surface have higher proportions of oxides. Such a construction will further increase the adhesion with respect to theplug body 11. The volume ratio of oxides can be determined by observing a cross section of the sprayedcoating 12 and doing calculations. - In the
piercer plug 10 according to the present embodiment, the chromium concentration determined by analyzing the sprayedcoating 12 with X-ray fluorescence analysis (hereinafter referred to as "XRF-Cr concentration") is 3 to 20 mass %. - An XRF-Cr concentration of 3 mass % or higher provides a better wear resistance than a concentration below 3 mass %. This is presumably because the complex oxides of iron and chromium increase the hardness of the sprayed
coating 12. On the other hand, an XRF-Cr concentration exceeding 20 mass % results in insufficient lubrication of the sprayedcoating 12, which reduces piercing efficiency. The lower limit for XRF-Cr concentration is preferably 5 mass %, and more preferably 8 mass %. The upper limit for XRF-Cr concentration is preferably 18 mass %, and more preferably 16 mass %. - XRF-Cr concentration can be measured in the following manner: an X-ray is directed into the sprayed
coating 12 through its surface, and the resulting X-ray fluorescence is detected with a detector. The incident X-ray is generated by a 3 mm ø spot collimator with a target of Rh and an output of 40 kV × 100 pA. The detector is a Si drift detector. The concentration of Cr is determined as a mass percentage, where the denominator is the total amount of all the elements detected. The numerator for XRF-Cr concentration includes both the Cr amount in the iron-based alloy and the Cr amount in the oxides. - Preferably, in the
piercer plug 10 according to the present embodiment, the iron concentration determined by analyzing the sprayedcoating 12 with X-ray fluorescence analysis is 50 mass % or higher. The determination of iron concentration by analyzing the coating with X-ray fluorescence analysis involves the same measurement method as for XRF-Cr concentration. - An exemplary method for manufacturing the
piercer plug 10 will be described below. The method described below is exemplary only, and a method for manufacturing thepiercer plug 10 is not limited thereto. -
Aplug body 11 is prepared. Theplug body 11 may be any plug body known to a person skilled in the art. - A sprayed
coating 12 is formed on theplug body 11. The sprayedcoating 12 may be formed using anarc sprayer 20, shown inFIG. 2 . - The arc sprayer 20 includes a spraying
gun 21 and a rotatingbase 24. The sprayinggun 21 generates an arc at the tips of a positive-electrode wire 22 and a negative-electrode wire 23 to melt metal, which is then ejected by means of compressed air. - The chemical composition of, and the XRF-Cr concentration in, the sprayed
coating 12 may be regulated by adjusting the chemical compositions of the positive- and negative- 22 and 23. The positive- andelectrode wires 22 and 23 may have the same chemical composition or may have different chemical compositions. If wires of different chemical compositions are used, metal from the positive-negative electrode wires electrode wire 22 and metal from the negative-electrode wire 23 mix together to form a pseudo-alloy. - Although not limiting, the positive- and negative-
22 and 23 may be made of carbon steel or stainless steel, for example. Alternatively, the positive- and negative-electrode wires 22 and 23 may be made of coredelectrode wires wire 30, shown inFIG. 3 . The coredwire 30 includes anouter sheath 31 made from carbon steel and afiller 32 filling theouter sheath 31. The chemical composition of the metal ejected from the sprayinggun 21 may be changed at will by changing the type of thefiller 32. - The longer the distance between the tip of the spraying
gun 21 and the surface of the plug body 11 (hereinafter referred to as "spraying distance"), the higher the proportion of oxides in the sprayedcoating 12. This is because the oxidation of metal ejected from the tip of the sprayinggun 21 progresses along the spraying distance. Although not limiting, the spraying distance may be 100 to 1400 mm, for example. Further, spraying at gradually increasing spraying distances results in higher proportions of metal in portions near theplug body 11 and higher proportions of oxides in portions located toward the surface. - As discussed above, the numerator for XRF-Cr concentration includes both the Cr amount in the iron-based alloy and the Cr amount in the oxides. As such, the XRF-Cr concentration does not significantly change even if the proportion of oxides in the sprayed
coating 12 changes. Thus, the XRF-Cr concentration does not significantly change even when the spraying distance is changed. - Spraying is performed while the rotating
base 24 rotates theplug body 11 about its axis until the thickness of the sprayedcoating 12 reaches a predetermined level. Although not limiting, the thickness of the sprayedcoating 12 may be 200 to 3000 µm, for example. - Preferably, the formation of the sprayed
coating 12 is followed by heat treatment for diffusion purposes. This achieves higher adhesion between theplug body 11 and sprayedcoating 12. For the heat treatment for diffusion purposes, the plug is preferably held at 600 to 1250 °C for 10 minutes or longer, for example. The heat-treatment temperature is more preferably 600 to 1100 °C. - The piercer plug 10 according to an embodiment of the present invention has been described. In the present embodiment, the XRF-Cr concentration in the sprayed
coating 12 is 3 to 20 mass %. This will increase the wear resistance of thepiercer plug 10. - The above-described embodiment illustrates an implementation where the
plug body 11 is projectile-shaped. However, theplug body 11 may have any shape. For example, the piercer plug may be aplug body 13 with a protruding tip, as shown inFIG. 4 , with a sprayedcoating 12 formed thereon, or may be a plug body 14 of a divided construction, as shown inFIG. 5 , with a sprayedcoating 12 formed thereon. - The above-described embodiments illustrate implementations where the sprayed
coating 12 is formed by arc spraying. However, a method for forming the sprayedcoating 12 is not limited thereto. The sprayedcoating 12 may be formed by, for example, plasma spraying, flame spraying, highspeed flame spraying, etc. - The present invention will now be described more specifically by means of examples. The present invention is not limited to these examples.
- A model plug mainly composed of 0.15 C, 0.5 Si, 1.0 Ni, 0.5 Mn, 1.5 Mo, 3.0 W, and balance Fe was prepared and a sprayed coating was formed thereon. A positive-electrode wire and a negative-electrode wire were prepared by combining wires of a low-carbon steel, SUS 410 and SUS 430, and cored wires with different Cr concentrations to adjust the compound of the sprayed coating to be formed.
- The XRF-Cr concentration in the sprayed coating was analyzed by the method described in connection with the embodiment. The X-ray fluorescence analyzer used was DP-2000 Delta Premium from JEOL Ltd., and the analysis was performed using ALLOY PLUS alloy analysis software from JEOL Ltd.
- The Vickers hardness of the sprayed coating of each plug was measured. The Vickers hardness of each plug was obtained by conducting three-point measurement and determining the average of the measurements.
- Table 1 shows the relationship between XRF-Cr concentration and average hardness. In Table 1, "-" in the column for XRF-Cr concentration indicates that the XRF-Cr concentration was below the lower limit for analysis.
[Table 1]TABLE 1 Mark XRF-Cr concentration (mass %) Vickers hardness (Hv) A - 320 B 1.04 345 C 3.03 380 D 7.85 400 E 11.52 450 F 15.53 500 G 18.11 520 H 22.30 550 - As shown in Table ,1 the higher the XRF-Cr concentration, the higher the average Vickers hardness.
-
FIG. 6 shows a cross-sectional microphotograph of the sprayed coating labeled Mark A in Table 1.FIG. 7 shows a cross-sectional microphotograph of the sprayed coating labeled Mark C in Table 1. As illustrated inFIG. 7 , a sprayed coating containing Cr was composed of metal and oxides, similar to the sprayed coating containing no Cr (FIG. 6 ). In these figures, relatively bright portions represent portions made from metal, while dark-gray portions represent portions made from oxides. The ratio between metal and oxides was substantially the same for each of the sprayed coatings prepared for the present application, where the proportion of oxides was about 44 to 55 vol%. - Subsequently, these plugs were used to conduct piercing tests, where the material to be processed was SUS 304, to measure the amount of wear of the coating. Table 2 shows the relationship between XRF-Cr concentration and amount of wear. The column labeled "Ratio of wear to conventional" in Table 2 lists the relative amounts of wear for the sprayed coatings of the plugs, where the amount of wear for the sprayed coating of the plug labeled Mark A represents the value 1.
[Table 2]TABLE 2 Mark XRF-Cr concentration (mass %) Ratio of wear to conventional Notes Remarks A - 1 (reference) - comp. ex. B 1.04 0.95 - comp. ex. C 3.03 0.70 - inv. ex. D 7.85 0.70 - inv. ex. E 11.52 0.60 - inv. ex. F 15.53 0.40 - inv. ex. G 18.11 0.50 - inv. ex. H 22.30 0.11 low piercing efficiency comp. ex. - As shown in Table 2, the higher the XRF-Cr concentration, the smaller the amount of wear. Particularly, an XRF-Cr concentration of 3 mass % or higher resulted in a reduced amount of wear of up to about 70 % of the level for Mark A. On the other hand, an XRF-Cr concentration exceeding 20 mass % resulted in a reduction in piercing efficiency, making rolling difficult.
- These results prove that an XRF-Cr concentration in the range of 3 to 20 mass % increases the wear resistance of a piercer plug.
- Although embodiments of the present invention have been described, the above-described embodiments are exemplary only, intended to allow the present invention to be carried out. Accordingly, the present invention is not limited to the above-described embodiments, and the above-described embodiments, when carried out, may be modified as appropriate without departing from the spirit of the invention.
Claims (1)
- A piercer plug, comprising:a plug body; anda sprayed coating formed on a surface of the plug body,
the sprayed coating containing an iron-based alloy and an oxide of the iron-based alloy,
a chromium concentration determined by analyzing the sprayed coating with X-ray fluorescence analysis being 3 to 20 mass %.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2018047307 | 2018-03-14 | ||
| PCT/JP2019/001486 WO2019176279A1 (en) | 2018-03-14 | 2019-01-18 | Piercer plug |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| EP3767002A4 EP3767002A4 (en) | 2021-01-20 |
| EP3767002A1 true EP3767002A1 (en) | 2021-01-20 |
| EP3767002B1 EP3767002B1 (en) | 2024-08-28 |
Family
ID=67907651
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP19767149.8A Active EP3767002B1 (en) | 2018-03-14 | 2019-01-18 | Piercer plug |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US20210101194A1 (en) |
| EP (1) | EP3767002B1 (en) |
| JP (1) | JP6954447B2 (en) |
| CN (1) | CN111836911A (en) |
| MX (1) | MX2020007617A (en) |
| WO (1) | WO2019176279A1 (en) |
Family Cites Families (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5913924B2 (en) * | 1979-12-25 | 1984-04-02 | 日本鋼管株式会社 | Core metal for piercing rolling mill |
| JPH01154808A (en) * | 1987-12-11 | 1989-06-16 | Nippon Steel Corp | Tool for drawing steel tube |
| JPH03204106A (en) * | 1989-12-28 | 1991-09-05 | Sumitomo Metal Ind Ltd | Plug for manufacturing hot seamless tube |
| JP4346780B2 (en) * | 2000-03-06 | 2009-10-21 | 新日鉄マテリアルズ株式会社 | Heat-resistant and wear-resistant composite structural member and manufacturing method thereof |
| EP2198984B1 (en) | 2007-11-01 | 2016-12-14 | Nippon Steel & Sumitomo Metal Corporation | Piercing plug, method for regenerating piercing plug, and regeneration facility line for piercing plug |
| UA97027C2 (en) * | 2007-11-01 | 2011-12-26 | Сумитомо Мэтал Индастриз, Лтд. | Piercing and rolling plug, method of regenerating piercing and rolling plug and regeneration facility for piercing and rolling plug |
| EP2837434B1 (en) * | 2012-04-11 | 2018-01-17 | Nippon Steel & Sumitomo Metal Corporation | Plug used in piercing machine and plug regeneration method |
| JP5365724B2 (en) * | 2012-04-24 | 2013-12-11 | 新日鐵住金株式会社 | Equipment for manufacturing piercing and rolling plugs |
| JP5365723B2 (en) * | 2012-04-24 | 2013-12-11 | 新日鐵住金株式会社 | Manufacturing method of piercing and rolling plug |
| JP6136625B2 (en) * | 2012-06-25 | 2017-05-31 | 新日鐵住金株式会社 | Lubricant for hot working, lubricating coating and hot working method |
| BR112014030092A2 (en) * | 2012-07-20 | 2017-06-27 | Nippon Steel & Sumitomo Metal Corp | plug for piercing |
| JP5445724B1 (en) | 2012-08-28 | 2014-03-19 | 新日鐵住金株式会社 | Perforated plug and method for manufacturing perforated plug |
| JP6540441B2 (en) * | 2015-10-06 | 2019-07-10 | 日本製鉄株式会社 | Plug manufacturing method |
| WO2019087510A1 (en) * | 2017-11-02 | 2019-05-09 | 日本製鉄株式会社 | Piercing plug and manufacturing method therefor |
-
2019
- 2019-01-18 MX MX2020007617A patent/MX2020007617A/en unknown
- 2019-01-18 EP EP19767149.8A patent/EP3767002B1/en active Active
- 2019-01-18 JP JP2020505625A patent/JP6954447B2/en active Active
- 2019-01-18 US US16/971,149 patent/US20210101194A1/en not_active Abandoned
- 2019-01-18 CN CN201980018646.3A patent/CN111836911A/en active Pending
- 2019-01-18 WO PCT/JP2019/001486 patent/WO2019176279A1/en not_active Ceased
Also Published As
| Publication number | Publication date |
|---|---|
| JPWO2019176279A1 (en) | 2021-01-07 |
| WO2019176279A1 (en) | 2019-09-19 |
| BR112020014527A2 (en) | 2020-12-08 |
| JP6954447B2 (en) | 2021-10-27 |
| US20210101194A1 (en) | 2021-04-08 |
| EP3767002A4 (en) | 2021-01-20 |
| MX2020007617A (en) | 2020-09-14 |
| CN111836911A (en) | 2020-10-27 |
| EP3767002B1 (en) | 2024-08-28 |
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