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WO2019176279A1 - Piercer plug - Google Patents

Piercer plug Download PDF

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Publication number
WO2019176279A1
WO2019176279A1 PCT/JP2019/001486 JP2019001486W WO2019176279A1 WO 2019176279 A1 WO2019176279 A1 WO 2019176279A1 JP 2019001486 W JP2019001486 W JP 2019001486W WO 2019176279 A1 WO2019176279 A1 WO 2019176279A1
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WO
WIPO (PCT)
Prior art keywords
plug
thermal spray
spray coating
oxide
concentration
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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.)
Ceased
Application number
PCT/JP2019/001486
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French (fr)
Japanese (ja)
Inventor
日高 康善
東田 泰斗
尚也 白沢
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Nippon Steel Corp
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Nippon Steel Corp
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Filing date
Publication date
Application filed by Nippon Steel Corp filed Critical Nippon Steel Corp
Priority to BR112020014527-0A priority Critical patent/BR112020014527B1/en
Priority to JP2020505625A priority patent/JP6954447B2/en
Priority to CN201980018646.3A priority patent/CN111836911A/en
Priority to MX2020007617A priority patent/MX2020007617A/en
Priority to EP19767149.8A priority patent/EP3767002B1/en
Priority to US16/971,149 priority patent/US20210101194A1/en
Publication of WO2019176279A1 publication Critical patent/WO2019176279A1/en
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

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    • BPERFORMING OPERATIONS; TRANSPORTING
    • B21MECHANICAL METAL-WORKING WITHOUT ESSENTIALLY REMOVING MATERIAL; PUNCHING METAL
    • B21BROLLING OF METAL
    • B21B25/00Mandrels 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
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/02Ferrous alloys, e.g. steel alloys containing silicon
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/04Ferrous alloys, e.g. steel alloys containing manganese
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/08Ferrous alloys, e.g. steel alloys containing nickel
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/12Ferrous alloys, e.g. steel alloys containing tungsten, tantalum, molybdenum, vanadium, or niobium
    • CCHEMISTRY; METALLURGY
    • C23COATING 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
    • C23CCOATING 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
    • C23C30/00Coating with metallic material characterised only by the composition of the metallic material, i.e. not characterised by the coating process
    • CCHEMISTRY; METALLURGY
    • C23COATING 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
    • C23CCOATING 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
    • C23C4/00Coating by spraying the coating material in the molten state, e.g. by flame, plasma or electric discharge
    • C23C4/04Coating by spraying the coating material in the molten state, e.g. by flame, plasma or electric discharge characterised by the coating material
    • C23C4/06Metallic material
    • CCHEMISTRY; METALLURGY
    • C23COATING 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
    • C23CCOATING 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
    • C23C4/00Coating by spraying the coating material in the molten state, e.g. by flame, plasma or electric discharge
    • C23C4/04Coating by spraying the coating material in the molten state, e.g. by flame, plasma or electric discharge characterised by the coating material
    • C23C4/10Oxides, borides, carbides, nitrides or silicides; Mixtures thereof
    • C23C4/11Oxides
    • CCHEMISTRY; METALLURGY
    • C23COATING 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
    • C23CCOATING 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
    • C23C4/00Coating by spraying the coating material in the molten state, e.g. by flame, plasma or electric discharge
    • C23C4/12Coating by spraying the coating material in the molten state, e.g. by flame, plasma or electric discharge characterised by the method of spraying
    • C23C4/123Spraying molten metal
    • CCHEMISTRY; METALLURGY
    • C23COATING 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
    • C23CCOATING 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
    • C23C4/00Coating by spraying the coating material in the molten state, e.g. by flame, plasma or electric discharge
    • C23C4/12Coating by spraying the coating material in the molten state, e.g. by flame, plasma or electric discharge characterised by the method of spraying
    • C23C4/129Flame spraying
    • CCHEMISTRY; METALLURGY
    • C23COATING 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
    • C23CCOATING 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
    • C23C4/00Coating by spraying the coating material in the molten state, e.g. by flame, plasma or electric discharge
    • C23C4/12Coating by spraying the coating material in the molten state, e.g. by flame, plasma or electric discharge characterised by the method of spraying
    • C23C4/131Wire arc spraying
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B21MECHANICAL METAL-WORKING WITHOUT ESSENTIALLY REMOVING MATERIAL; PUNCHING METAL
    • B21BROLLING OF METAL
    • B21B19/00Tube-rolling by rollers arranged outside the work and having their axes not perpendicular to the axis of the work
    • B21B19/02Tube-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
    • B21B19/04Rolling basic material of solid, i.e. non-hollow, structure; Piercing, e.g. rotary piercing mills

Definitions

  • FIG. 1 is a longitudinal 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 thermal spray coating 12.
  • the iron-based alloy in the thermal spray coating 12 is mainly composed of iron (Fe) and contains carbon (C), silicon (Si), manganese (Mn), chromium (Cr), and the like.
  • the iron-based alloy in the thermal spray coating 12 may contain only a part of C, Si, Mn, and Cr, or may contain elements other than C, Si, Mn, and Cr.
  • the chemical composition of the iron-based alloy in the thermal spray coating 12 may not be microscopically uniform. For example, microscopically, a portion that hardly contains Cr and a portion that has a high Cr content may be mixed.
  • the oxide in the thermal spray coating 12 is an oxide formed by oxidizing the iron-based alloy.
  • Specific examples of the oxide in the thermal spray coating 12 include iron oxide and a composite oxide of iron and chromium.
  • the iron oxide include FeO and Fe 3 O 4 .
  • the composite oxide of iron and chromium is, for example, (Fe, Cr) 3 O 4 .
  • the oxide in the sprayed coating 12 may contain a metal oxide other than the above.
  • the ratio of the oxide in the thermal spray coating 12 is not limited to this, but is preferably 25 to 80% by volume, more preferably 35 to 65% by volume. Moreover, it is preferable that the ratio of a metal component is high in the vicinity of the plug main body 11, and the ratio of an oxide becomes high as it goes to the surface. According to this configuration, the adhesiveness with the plug body 11 can be further increased.
  • the volume ratio of the oxide can be calculated from cross-sectional observation of the sprayed coating 12.
  • thermal spray distance The longer the distance from the tip of the thermal spray gun 21 to the surface of the plug body 11 (hereinafter referred to as “thermal spray distance”), the higher the ratio of oxide in the thermal spray coating 12. This is because the oxidation of the metal sprayed from the tip of the spray gun 21 proceeds according to the spray distance.
  • the spraying distance is not limited to this, but is, for example, 100 to 1400 mm. Further, by spraying while gradually increasing the spraying distance, the ratio of the metal component in the vicinity of the plug body 11 can be increased, and the ratio of the oxide can be increased toward the surface.
  • the thickness of the sprayed coating 12 is not limited to this, but is, for example, 200 to 3000 ⁇ m.
  • the piercer plug 10 according to the embodiment of the present invention has been described above.
  • the XRF-Cr concentration of the thermal spray coating 12 is 3 to 20% by mass. Thereby, the wear resistance of the piercer plug 10 can be further improved.
  • the thermal spray coating 12 can be formed by, for example, plasma spraying, flame spraying, high-speed flame spraying, or the like.

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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

Provided is a piercer plug having further improved wear resistance. The piercer plug (10) is equipped with a plug body (11) and a sprayed coating film (12) formed on the surface of the plug body (11). The sprayed coating film (12) includes an iron-based alloy and an oxide thereof. The chromium concentration obtained by analyzing the sprayed coating film (12) by fluorescent x-ray analysis is 3-20% by mass.

Description

ピアサープラグPiercer plug

 本発明は、ピアサープラグに関する。 The present invention relates to a piercer plug.

 従来、継目無鋼管の穿孔圧延に用いられるピアサープラグは、表面の遮熱性、潤滑性、及び耐焼付き性を確保するため、表面にスケール皮膜を形成して使用される。 Conventionally, piercer plugs used for piercing and rolling of seamless steel pipes are used by forming a scale film on the surface in order to ensure surface thermal insulation, lubricity, and seizure resistance.

 スケール皮膜は、穿孔圧延ごとに次第に摩耗する。スケール皮膜が完全に摩耗して母材(プラグ本体)が露出すると、母材の溶損や相手材との焼付きが生じる。ステンレス等の難加工材の穿孔ではスケール皮膜の摩耗が顕著であり、数パスで摩耗する場合がある。その度にスケール皮膜を再形成するための熱処理が必要になるが、この熱処理には数時間から数十時間を要するため、能率が悪いという問題がある。 The scale film gradually wears with each piercing and rolling. When the scale film is completely worn and the base material (plug body) is exposed, the base material is melted and seized with the counterpart material. In the drilling of difficult-to-process materials such as stainless steel, the wear of the scale film is noticeable and may be worn in several passes. Each time, heat treatment for re-forming the scale film is required, but this heat treatment requires several hours to several tens of hours, and thus there is a problem that efficiency is poor.

 国際公開第2009/057471号には、鉄及び酸化物からなる溶射皮膜をピアサープラグの母材の表面に形成する技術が提案されている。国際公開第2014/034376号には、鉄及び鉄酸化物の他に、質量%で、C:0.015~0.6%、Si:0.05~0.5%、Mn:0.1~1.0%、Cu:0~0.3%を含有する溶射皮膜を備えたピアサープラグが開示されている。 International Publication No. 2009/057471 proposes a technique for forming a sprayed coating made of iron and oxide on the surface of a base material of a piercer plug. In WO2014 / 034376, in addition to iron and iron oxide, in mass%, C: 0.015 to 0.6%, Si: 0.05 to 0.5%, Mn: 0.1 A piercer plug with a thermal spray coating containing ˜1.0% and Cu: 0˜0.3% is disclosed.

 溶射皮膜は、スケール皮膜よりも母材との密着性や耐摩耗性に優れ、かつ、数分から数十分で形成することができる。そのため溶射皮膜は、スケール皮膜よりも寿命が長く、かつ、摩耗しても短時間で再生することができる。一方、継目無鋼管の製造能率を高めるためには、ピアサープラグの寿命をさらに長くすることが好ましい。そのためには、皮膜の耐摩耗性をさらに高くすることが好ましい。 The thermal spray coating has better adhesion to the base material and wear resistance than the scale coating, and can be formed in several minutes to several tens of minutes. Therefore, the thermal spray coating has a longer life than the scale coating and can be regenerated in a short time even when worn. On the other hand, in order to increase the production efficiency of the seamless steel pipe, it is preferable to further increase the life of the piercer plug. For this purpose, it is preferable to further increase the wear resistance of the coating.

 本発明の目的は、耐摩耗性をさらに高めたピアサープラグを提供することである。 An object of the present invention is to provide a piercer plug with further improved wear resistance.

 本発明の一実施形態によるピアサープラグは、プラグ本体と、前記プラグ本体の表面に形成された溶射皮膜とを備える。前記溶射皮膜は、鉄基合金及び前記鉄基合金の酸化物を含む。前記溶射皮膜を蛍光X線分析で分析して得られるクロム濃度が、3~20質量%である。 A piercer plug according to an embodiment of the present invention includes a plug body and a thermal spray coating formed on the surface of the plug body. The thermal spray coating includes an iron-based alloy and an oxide of the iron-based alloy. The chromium concentration obtained by analyzing the sprayed coating by fluorescent X-ray analysis is 3 to 20% by mass.

 本発明によれば、耐摩耗性をさらに高めたピアサープラグが得られる。 According to the present invention, a piercer plug with further improved wear resistance can be obtained.

図1は、本発明の一実施形態によるピアサープラグの縦断面図である。FIG. 1 is a longitudinal sectional view of a piercer plug according to an embodiment of the present invention. 図2は、溶射皮膜の形成に用いる装置の一例を示す図である。FIG. 2 is a diagram illustrating an example of an apparatus used for forming a thermal spray coating. 図3は、コアードワイヤの断面図である。FIG. 3 is a cross-sectional view of a cored wire. 図4は、本発明の他の実施形態によるピアサープラグの縦断面図である。FIG. 4 is a longitudinal sectional view of a piercer plug according to another embodiment of the present invention. 図5は、本発明のさらに他の実施形態によるピアサープラグの縦断面図である。FIG. 5 is a longitudinal sectional view of a piercer plug according to still another embodiment of the present invention. 図6は、Crを含まない溶射皮膜の断面顕微鏡写真である。FIG. 6 is a cross-sectional photomicrograph of a thermal spray coating not containing Cr. 図7は、Crを含む溶射皮膜の断面顕微鏡写真である。FIG. 7 is a cross-sectional micrograph of a sprayed coating containing Cr.

 以下、図面を参照し、本発明の実施の形態を詳しく説明する。図中同一又は相当部分には同一符号を付してその説明は繰り返さない。各図に示された構成部材間の寸法比は、必ずしも実際の寸法比を示すものではない。 Hereinafter, embodiments of the present invention will be described in detail with reference to the drawings. In the drawings, the same or corresponding parts are denoted by the same reference numerals and description thereof will not be repeated. The dimensional ratio between the constituent members shown in each drawing does not necessarily indicate the actual dimensional ratio.

 [ピアサープラグの構造]
 図1は、本発明の一実施形態によるピアサープラグ10の縦断面図である。ピアサープラグ10は、プラグ本体11と、溶射皮膜12とを備えている。
[Piercer plug structure]
FIG. 1 is a longitudinal 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 thermal spray coating 12.

 プラグ本体11は、砲弾形状を有する。プラグ本体11は、具体的には、横断面の形状が円形であり、その外径がプラグ本体11の先端から後端に向かって大きくなる形状を有している。プラグ本体11は、例えば、鉄基合金で構成されている。 The plug body 11 has a shell shape. Specifically, the plug main body 11 has a circular cross-sectional shape and an outer diameter that increases from the front end of the plug main body 11 toward the rear end. The plug body 11 is made of, for example, an iron-based alloy.

 溶射皮膜12は、プラグ本体11の表面に形成されている。溶射皮膜12は、プラグ本体11の後端面を除き、プラグ本体11の表面の全体を覆っている。溶射皮膜12の厚さは、一定でなくてもよい。溶射皮膜12は、プラグ本体11の胴部11b上よりも先端部11a上に厚く形成されていることが好ましい。 The thermal spray coating 12 is formed on the surface of the plug body 11. The thermal spray 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 thermal spray coating 12 is preferably formed thicker on the distal end portion 11 a than on the body portion 11 b of the plug body 11.

 溶射皮膜12は、少なくとも鉄基合金及びその酸化物を含んでいる。溶射皮膜12は、これら以外の化合物を含んでいてもよい。 The sprayed coating 12 contains at least an iron-based alloy and its oxide. The sprayed coating 12 may contain a compound other than these.

 溶射皮膜12中の鉄基合金は、鉄(Fe)を主成分とし、炭素(C)、シリコン(Si)、マンガン(Mn)、及びクロム(Cr)等を含んでいる。溶射皮膜12中の鉄基合金は、C、Si、Mn、及びCrのうちの一部のみを含んでいてもよいし、C、Si、Mn、及びCr以外の元素を含んでいてもよい。溶射皮膜12中の鉄基合金の化学組成は微視的には一様でなくてもよい。例えば、微視的にはCrを殆ど含まない部分とCr含有量の高い部分とが混在していてもよい。 The iron-based alloy in the thermal spray coating 12 is mainly composed of iron (Fe) and contains carbon (C), silicon (Si), manganese (Mn), chromium (Cr), and the like. The iron-based alloy in the thermal spray coating 12 may contain only a part of C, Si, Mn, and Cr, or may contain elements other than C, Si, Mn, and Cr. The chemical composition of the iron-based alloy in the thermal spray coating 12 may not be microscopically uniform. For example, microscopically, a portion that hardly contains Cr and a portion that has a high Cr content may be mixed.

 溶射皮膜12中の酸化物は、上記の鉄基合金が酸化されて形成される酸化物である。溶射皮膜12中の酸化物は、具体的には、鉄酸化物、及び鉄とクロムとの複合酸化物等である。鉄酸化物は、例えばFeO、Fe等である。鉄とクロムとの複合酸化物は例えば、(Fe,Cr)等である。溶射皮膜12中の酸化物は、上記以外の金属の酸化物を含んでいてもよい。 The oxide in the thermal spray coating 12 is an oxide formed by oxidizing the iron-based alloy. Specific examples of the oxide in the thermal spray coating 12 include iron oxide and a composite oxide of iron and chromium. Examples of the iron oxide include FeO and Fe 3 O 4 . The composite oxide of iron and chromium is, for example, (Fe, Cr) 3 O 4 . The oxide in the sprayed coating 12 may contain a metal oxide other than the above.

 溶射皮膜12中、金属成分(鉄基合金)の比率が高いほど、プラグ本体11との密着性が向上する。一方、酸化物の比率が高いほど、遮熱性が向上する。溶射皮膜12中の酸化物の比率は、これに限定されないが、好ましくは25~80体積%であり、さらに好ましくは35~65体積%である。また、プラグ本体11の近傍は金属成分の比率が高く、表面に向かうにつれて酸化物の比率が高くなることが好ましい。この構成によれば、プラグ本体11との密着性をより高くすることができる。なお、酸化物の体積率は、溶射皮膜12の断面観察から算出することができる。 The higher the ratio of the metal component (iron-based alloy) in the sprayed coating 12, the better the adhesion with the plug body 11. On the other hand, the higher the oxide ratio, the better the heat shielding properties. The ratio of the oxide in the thermal spray coating 12 is not limited to this, but is preferably 25 to 80% by volume, more preferably 35 to 65% by volume. Moreover, it is preferable that the ratio of a metal component is high in the vicinity of the plug main body 11, and the ratio of an oxide becomes high as it goes to the surface. According to this configuration, the adhesiveness with the plug body 11 can be further increased. The volume ratio of the oxide can be calculated from cross-sectional observation of the sprayed coating 12.

 本実施形態によるピアサープラグ10は、溶射皮膜12を蛍光X線分析で分析して得られるクロム濃度(以下「XRF-Cr濃度」という。)が、3~20質量%である。 The piercer plug 10 according to the present embodiment has a chromium concentration (hereinafter referred to as “XRF-Cr concentration”) obtained by analyzing the sprayed coating 12 by fluorescent X-ray analysis of 3 to 20 mass%.

 XRF-Cr濃度が3質量%以上であれば、3質量%未満の場合と比較して、優れた耐摩耗性が得られる。これは、鉄とクロムとの複合酸化物によって溶射皮膜12の硬度が高くなるためと考えられる。一方、XRF-Cr濃度が20質量%を超えると、溶射皮膜12の潤滑性が低下し、穿孔効率が低下する。XRF-Cr濃度の下限は、好ましくは5質量%であり、さらに好ましくは8質量%である。XRF-Cr濃度の上限は、好ましくは18質量%であり、さらに好ましくは16質量%である。 When the XRF-Cr concentration is 3% by mass or more, excellent wear resistance is obtained as compared with the case of less than 3% by mass. This is presumably because the hardness of the thermal spray coating 12 is increased by the composite oxide of iron and chromium. On the other hand, if the XRF-Cr concentration exceeds 20% by mass, the lubricity of the thermal spray coating 12 decreases and the perforation efficiency decreases. The lower limit of the XRF-Cr concentration is preferably 5% by mass, more preferably 8% by mass. The upper limit of the XRF-Cr concentration is preferably 18% by mass, and more preferably 16% by mass.

 XRF-Cr濃度は、下記のように測定する。溶射皮膜12の表面からX線を入射し、検出器で蛍光X線を検出する。入射X線は、ターゲット:Rh、出力:40kV×100μA、3mmΦスポットコリメーターを適用する。検出器は、Si drift detectorとする。検出されたすべての元素を分母として、Crの濃度を質量%で求める。XRF-Cr濃度の分子には、鉄基合金中のCrと酸化物中のCrとの両方が含まれる。 XRF-Cr concentration is measured as follows. X-rays are incident from the surface of the thermal spray coating 12, and the fluorescent X-rays are detected by a detector. For incident X-rays, target: Rh, output: 40 kV × 100 μA, 3 mmΦ spot collimator is applied. The detector is a Si drift detector. Using all the detected elements as the denominator, the Cr concentration is determined by mass%. The XRF-Cr concentration molecules include both Cr in the iron-base alloy and Cr in the oxide.

 本実施形態によるピアサープラグ10は、好ましくは、溶射皮膜12を蛍光X線分析で分析して得られる鉄濃度が、50質量%以上である。蛍光X線分析で分析して得られる鉄濃度は、XRF-Cr濃度と同様に測定する。 The piercer plug 10 according to the present embodiment preferably has an iron concentration obtained by analyzing the sprayed coating 12 by fluorescent X-ray analysis of 50% by mass or more. The iron concentration obtained by analysis by fluorescent X-ray analysis is measured in the same manner as the XRF-Cr concentration.

 [ピアサープラグの製造方法]
 以下、ピアサープラグ10の製造方法の一例を説明する。以下で説明する方法はあくまで例示であり、ピアサープラグ10の製造方法はこれに限定されない。
[Piercer plug manufacturing method]
Hereinafter, an example of the manufacturing method of the piercer plug 10 will be described. The method described below is merely an example, and the manufacturing method of the piercer plug 10 is not limited to this.

 プラグ本体11を準備する。プラグ本体11は、公知のものを用いることができる。 Prepare the plug body 11. A known plug body 11 can be used.

 プラグ本体11に、溶射皮膜12を形成する。溶射皮膜12は、図2に示すアーク溶射装置20を用いて形成することができる。 The thermal spray coating 12 is formed on the plug body 11. The sprayed coating 12 can be formed using the arc spraying apparatus 20 shown in FIG.

 アーク溶射装置20は、溶射ガン21と、回転台24とを備えている。溶射ガン21は、連続的に供給される陽極線材22及び陰極線材23の先端でアークを発生させ、溶融した金属を圧縮空気によって噴射する。 The arc spray device 20 includes a spray gun 21 and a turntable 24. The spray gun 21 generates an arc at the tips of the anode wire 22 and the cathode wire 23 that are continuously supplied, and injects molten metal with compressed air.

 溶射皮膜12の化学組成及びXRF-Cr濃度は、陽極線材22及び陰極線材23の化学組成よって調整することができる。陽極線材22及び陰極線材23は、同じ化学組成の線材であってもよいし、異なる化学組成の線材であってもよい。異なる化学組成の線材を用いた場合、陽極線材22の金属と陰極線材23の金属とが混ざりあって、擬似的な合金が形成される。 The chemical composition and XRF-Cr concentration of the thermal spray coating 12 can be adjusted by the chemical composition of the anode wire 22 and the cathode wire 23. The anode wire 22 and the cathode wire 23 may be wires having the same chemical composition or may be wires having different chemical compositions. When wires having different chemical compositions are used, the metal of the anode wire 22 and the metal of the cathode wire 23 are mixed to form a pseudo alloy.

 陽極線材22及び陰極線材23は、これに限定されないが、例えば炭素鋼やステンレス鋼である。また、陽極線材22及び陰極線材23として、図3に示すコアードワイヤ30を用いてもよい。コアードワイヤ30は、炭素鋼製の外殻31と、外殻31に充填された充填材32とを備えている。充填材32の種類を変えることで、溶射ガン21から噴射する金属の化学組成を任意に変えることができる。 The anode wire 22 and the cathode wire 23 are not limited to this, but are, for example, carbon steel or stainless steel. Further, the cored wire 30 shown in FIG. 3 may be used as the anode wire 22 and the cathode wire 23. The cored wire 30 includes a carbon steel outer shell 31 and a filler 32 filled in the outer shell 31. By changing the type of the filler 32, the chemical composition of the metal sprayed from the spray gun 21 can be arbitrarily changed.

 溶射ガン21の先端からプラグ本体11の表面までの距離(以下「溶射距離」という。)が長いほど、溶射皮膜12中の酸化物の比率が高くなる。これは、溶射ガン21の先端から噴射される金属の酸化が溶射距離に応じて進行するためである。溶射距離は、これに限定されないが、例えば100~1400mmである。また、溶射距離を徐々に長くしながら溶射することで、プラグ本体11の近傍の金属成分の比率を高くし、表面に向かうにしたがって酸化物の比率を高くすることができる。 The longer the distance from the tip of the thermal spray gun 21 to the surface of the plug body 11 (hereinafter referred to as “thermal spray distance”), the higher the ratio of oxide in the thermal spray coating 12. This is because the oxidation of the metal sprayed from the tip of the spray gun 21 proceeds according to the spray distance. The spraying distance is not limited to this, but is, for example, 100 to 1400 mm. Further, by spraying while gradually increasing the spraying distance, the ratio of the metal component in the vicinity of the plug body 11 can be increased, and the ratio of the oxide can be increased toward the surface.

 上述のとおり、XRF-Cr濃度の分子には、鉄基合金中のCrと酸化物中のCrとの両方が含まれる。そのため、XRF-Cr濃度は、溶射皮膜12中の酸化物の比率が変わっても大きくは変化しない。そのため、XRF-Cr濃度は、溶射距離を変えても大きくは変化しない。 As described above, the molecule having the XRF-Cr concentration includes both Cr in the iron-based alloy and Cr in the oxide. Therefore, the XRF-Cr concentration does not change greatly even if the ratio of the oxide in the thermal spray coating 12 changes. Therefore, the XRF-Cr concentration does not change greatly even if the spraying distance is changed.

 回転台24によってプラグ本体11を軸周りに回転させながら、溶射皮膜12が所定の厚さになるまで溶射する。溶射皮膜12の厚さは、これに限定されないが、例えば200~3000μmである。 While the plug body 11 is rotated around the axis by the turntable 24, spraying is performed until the sprayed coating 12 reaches a predetermined thickness. The thickness of the sprayed coating 12 is not limited to this, but is, for example, 200 to 3000 μm.

 溶射皮膜12を形成後、拡散のための熱処理を実施することが好ましい。これによって、プラグ本体11と溶射皮膜12とをより密着させることができる。拡散のための熱処理として例えば、600~1250℃で10分以上保持することが好ましい。熱処理温度はより好ましくは600~1100℃である。 After forming the thermal spray coating 12, it is preferable to perform a heat treatment for diffusion. Thereby, the plug main body 11 and the thermal spray coating 12 can be more closely attached. For example, the heat treatment for diffusion is preferably held at 600 to 1250 ° C. for 10 minutes or more. The heat treatment temperature is more preferably 600 to 1100 ° C.

 以上、本発明の一実施形態によるピアサープラグ10を説明した。本実施形態では、溶射皮膜12のXRF-Cr濃度を3~20質量%にする。これによって、ピアサープラグ10の耐摩耗性をさらに高めることができる。 The piercer plug 10 according to the embodiment of the present invention has been described above. In this embodiment, the XRF-Cr concentration of the thermal spray coating 12 is 3 to 20% by mass. Thereby, the wear resistance of the piercer plug 10 can be further improved.

 上記の実施形態では、プラグ本体11が砲弾形状である場合を説明した。しかし、プラグ本体11の形状は任意である。ピアサープラグは例えば、図3に示す先端突出形状のプラグ本体13に溶射皮膜12が形成されたものであってもよいし、図4に示す分割形状のプラグ本体14に溶射皮膜12が形成されたものであってもよい。 In the above embodiment, the case where the plug body 11 has a bullet shape has been described. However, the shape of the plug body 11 is arbitrary. For example, the piercer plug may be one in which the spray coating 12 is formed on the plug body 13 having a protruding tip shape shown in FIG. 3, or the spray coating 12 is formed on the plug body 14 having a split shape shown in FIG. It may be a thing.

 上記の実施形態では、溶射皮膜12をアーク溶射によって形成する場合を説明した。しかし、溶射皮膜12を形成する方法はこれに限定されない。溶射皮膜12は例えば、プラズマ溶射、フレーム溶射、高速フレーム溶射等によって形成することもできる。 In the above embodiment, the case where the sprayed coating 12 is formed by arc spraying has been described. However, the method of forming the sprayed coating 12 is not limited to this. The thermal spray coating 12 can be formed by, for example, plasma spraying, flame spraying, high-speed flame spraying, or the like.

 以下、実施例によって本発明をより具体的に説明する。本発明はこれらの実施例に限定されない。 Hereinafter, the present invention will be described more specifically with reference to examples. The present invention is not limited to these examples.

 主要成分が0.15C-0.5Si-1.0Ni-0.5Mn-1.5Mo-3.0W-Bal.Feのモデルプラグの上に溶射皮膜を形成した。陽極線材及び陰極線材として、低炭素鋼、SUS410、及びSUS430の線材、並びにCr濃度を変化させたコアードワイヤを組み合わせて、溶射皮膜の成分を調整した。 The main component is 0.15C-0.5Si-1.0Ni-0.5Mn-1.5Mo-3.0W-Bal. A thermal spray coating was formed on the Fe model plug. As the anode wire and the cathode wire, low carbon steel, SUS410 and SUS430 wires, and a cored wire with a changed Cr concentration were combined to adjust the components of the thermal spray coating.

 実施形態で説明した方法によって、溶射皮膜のXRF-Cr濃度を分析した。蛍光X線分析装置はJEOL社製DP2000 DELTA Premiumを使用し、JEOL社製ALLOY PLUS 合金分析ソフトウエアを用いて解析した。 The XRF-Cr concentration of the thermal spray coating was analyzed by the method described in the embodiment. The fluorescent X-ray analyzer was analyzed using JEOL's DP2000 DELTA Premium, using JEOL's ALLOY PLUS alloy analysis software.

 各プラグの溶射皮膜のビッカース硬度を測定した。ビッカース硬度は、各プラグについて3点測定し、その平均を求めた。 The Vickers hardness of the sprayed coating of each plug was measured. The Vickers hardness was measured at three points for each plug, and the average was obtained.

 表1に、XRF-Cr濃度と平均硬度との関係を示す。表1において、XRF-Cr濃度の欄の「-」は、XRF-Cr濃度が分析下限未満であったことを示す。 Table 1 shows the relationship between the XRF-Cr concentration and the average hardness. In Table 1, “-” in the column of XRF-Cr concentration indicates that the XRF-Cr concentration was less than the lower limit of analysis.

Figure JPOXMLDOC01-appb-T000001
Figure JPOXMLDOC01-appb-T000001

 表1に示すように、XRF-Cr濃度が高いほど、平均ビッカース硬度が高くなった。 As shown in Table 1, the higher the XRF-Cr concentration, the higher the average Vickers hardness.

 図6は、表1のマークAの溶射皮膜の断面顕微鏡写真である。図7は、表1のマークCの溶射皮膜の断面顕微鏡写真である。図7に示すとおり、Crを含む溶射皮膜は、Crを含まない溶射皮膜(図6)と同様、金属成分と酸化物とから構成されていた。図中、比較的明るい部分が金属成分からなる箇所であり、濃いグレーの部分が酸化物からなる箇所である。金属成分と酸化物との比は、今回作成したすべての溶射皮膜で同程度であり、酸化物の比率が約45~55体積%であった。 FIG. 6 is a cross-sectional micrograph of the thermal spray coating of mark A in Table 1. FIG. 7 is a cross-sectional photomicrograph of the thermal spray coating of mark C in Table 1. As shown in FIG. 7, the thermal spray coating containing Cr was composed of a metal component and an oxide, like the thermal spray coating not containing Cr (FIG. 6). In the figure, a relatively bright portion is a portion made of a metal component, and a dark gray portion is a portion made of an oxide. The ratio of the metal component to the oxide was almost the same in all the sprayed coatings prepared this time, and the ratio of the oxide was about 45 to 55% by volume.

 続いて、これらのプラグを用いて、SUS304を相手材とした穿孔試験を実施し、皮膜摩耗量を測定した。表2に、XRF-Cr濃度と摩耗量との関係を示す。表2の「従来比摩耗量」の欄には、マークAのプラグの溶射皮膜の摩耗量を1として各プラグの溶射皮膜の摩耗量を相対値で記載している。 Subsequently, using these plugs, a drilling test was conducted using SUS304 as a counterpart material, and the amount of film abrasion was measured. Table 2 shows the relationship between the XRF-Cr concentration and the amount of wear. In the column of “Conventional specific wear amount” in Table 2, the wear amount of the thermal spray coating of the plug of the mark A is set to 1, and the wear amount of the thermal spray coating of each plug is described as a relative value.

Figure JPOXMLDOC01-appb-T000002
Figure JPOXMLDOC01-appb-T000002

 表2に示すように、XRF-Cr濃度が高いほど、摩耗量が低減した。特に、XRF-Cr濃度を3質量%以上にすることで、摩耗量をマークAの場合の約70%にまで低減することができた。一方、XRF-Cr濃度が20質量%を超えると、穿孔効率が低下し、圧延が困難になった。 As shown in Table 2, the higher the XRF-Cr concentration, the lower the wear amount. In particular, by setting the XRF-Cr concentration to 3% by mass or more, the amount of wear could be reduced to about 70% in the case of the mark A. On the other hand, when the XRF-Cr concentration exceeded 20% by mass, the drilling efficiency was lowered and rolling became difficult.

 これらの結果から、XRF-Cr濃度を3~20質量%にすることで、ピアサープラグの耐摩耗性をさらに高められることが裏付けられた。 These results confirmed that the wear resistance of the piercer plug can be further improved by setting the XRF-Cr concentration to 3 to 20% by mass.

 以上、本発明の実施形態を説明したが、上述した実施形態は本発明を実施するための例示にすぎない。よって、本発明は上述した実施形態に限定されることなく、その趣旨を逸脱しない範囲で、上述した実施形態を適宜変形して実施することが可能である。 As mentioned above, although embodiment of this invention was described, embodiment mentioned above is only the illustration for implementing this invention. Therefore, the present invention is not limited to the above-described embodiment, and can be implemented by appropriately modifying the above-described embodiment without departing from the spirit thereof.

Claims (1)

 プラグ本体と、
 前記プラグ本体の表面に形成された溶射皮膜とを備え、
 前記溶射皮膜は、鉄基合金及び前記鉄基合金の酸化物を含み、
 前記溶射皮膜を蛍光X線分析で分析して得られるクロム濃度が、3~20質量%である、ピアサープラグ。
A plug body;
A thermal spray coating formed on the surface of the plug body,
The thermal spray coating includes an iron-based alloy and an oxide of the iron-based alloy,
A piercer plug having a chromium concentration of 3 to 20% by mass obtained by analyzing the thermal spray coating by fluorescent X-ray analysis.
PCT/JP2019/001486 2018-03-14 2019-01-18 Piercer plug Ceased WO2019176279A1 (en)

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BR112020014527-0A BR112020014527B1 (en) 2018-03-14 2019-01-18 PUNCH PIN
JP2020505625A JP6954447B2 (en) 2018-03-14 2019-01-18 Piercer plug
CN201980018646.3A CN111836911A (en) 2018-03-14 2019-01-18 piercing mill head
MX2020007617A MX2020007617A (en) 2018-03-14 2019-01-18 Piercer plug.
EP19767149.8A EP3767002B1 (en) 2018-03-14 2019-01-18 Piercer plug
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