JP7179966B2 - Ferritic stainless steel sheets for automobile brake disc rotors, automobile brake disc rotors and hot stamped products for automobile brake disc rotors - Google Patents
Ferritic stainless steel sheets for automobile brake disc rotors, automobile brake disc rotors and hot stamped products for automobile brake disc rotors Download PDFInfo
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- JP7179966B2 JP7179966B2 JP2021509036A JP2021509036A JP7179966B2 JP 7179966 B2 JP7179966 B2 JP 7179966B2 JP 2021509036 A JP2021509036 A JP 2021509036A JP 2021509036 A JP2021509036 A JP 2021509036A JP 7179966 B2 JP7179966 B2 JP 7179966B2
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- C21D9/00—Heat treatment, e.g. annealing, hardening, quenching or tempering, adapted for particular articles; Furnaces therefor
- C21D9/46—Heat treatment, e.g. annealing, hardening, quenching or tempering, adapted for particular articles; Furnaces therefor for sheet metals
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- C22C38/004—Very low carbon steels, i.e. having a carbon content of less than 0,01%
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- B21—MECHANICAL METAL-WORKING WITHOUT ESSENTIALLY REMOVING MATERIAL; PUNCHING METAL
- B21D—WORKING OR PROCESSING OF SHEET METAL OR METAL TUBES, RODS OR PROFILES WITHOUT ESSENTIALLY REMOVING MATERIAL; PUNCHING METAL
- B21D22/00—Shaping without cutting, by stamping, spinning, or deep-drawing
- B21D22/02—Stamping using rigid devices or tools
- B21D22/022—Stamping using rigid devices or tools by heating the blank or stamping associated with heat treatment
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Description
本発明は、耐熱性と成形性に優れた、自動車ブレーキディスクローター用フェライト系ステンレス鋼板、自動車ブレーキディスクローター及び自動車ブレーキディスクローター用ホットスタンプ加工品に関するものであり、特に高温強度が必要な自動車ブレーキディスクローターなどの使用に好適なフェライト系ステンレス鋼板に関するものである。 TECHNICAL FIELD The present invention relates to a ferritic stainless steel sheet for automobile brake disc rotors, automobile brake disc rotors, and hot-stamped products for automobile brake disc rotors, which are excellent in heat resistance and formability, and particularly to automobile brakes that require high-temperature strength. The present invention relates to a ferritic stainless steel sheet suitable for use in disk rotors and the like.
自動車のブレーキシステムの一つとしてディスクブレーキが広く用いられている。これはタイヤと結合されたディスクローターと呼ばれる円盤状の構造物をブレーキパッドで押しはさむことで、摩擦によって運動エネルギーを熱エネルギーに変換し、自動車の速度を低下させるものである。このディスクローターの材質には熱伝導率やコスト等から片状黒鉛鋳鉄(以下、鋳鉄と呼ぶ)が用いられている。 Disc brakes are widely used as one of the braking systems of automobiles. By pressing a disc-shaped structure called a disc rotor, which is connected to the tire, between the brake pads, friction converts kinetic energy into thermal energy, slowing down the car. Flaky graphite cast iron (hereinafter referred to as cast iron) is used as the material of the disk rotor due to its thermal conductivity, cost, and the like.
鋳鉄は耐食性を向上させる元素が添加されていないため耐食性に劣り、放置するとすぐに赤さびが発生する。従来この赤さびはディスクの位置が視線より低いこととホイールの形状からあまり目立たなかった。しかし、近年の燃費向上の要請によりホイール材質がアルミニウム化され、またスポークが細くなることで、ディスクのさびが無視できないようになり、その耐食性の改善が望まれてきている。 Since cast iron does not contain any elements that improve corrosion resistance, it is inferior in corrosion resistance, and if left unattended, it quickly develops red rust. Conventionally, this red rust was not very noticeable due to the position of the disc below the line of sight and the shape of the wheel. However, due to the recent demand for improved fuel efficiency, wheels are being made of aluminum and spokes are getting thinner, so rust on discs can no longer be ignored, and improvements in corrosion resistance have been desired.
耐食性に優れる材料としてステンレス鋼があり、バイクなどの二輪車にはマルテンサイト系のSUS410系の材料が広く用いられている。これは二輪車のディスクローターがむき出しで人目につきやすく耐食性が重視されるためである。一方でステンレス鋼は熱伝導性が鋳鉄よりも劣るという課題がある。二輪車においてはブレーキシステムがむき出しで、冷却性に優れているためステンレス鋼でも問題なく使用されている。自動車の場合はタイヤを含むブレーキシステムがタイヤハウス内に収められているため、ディスクローターが冷却されにくく、熱伝導性が低いことが課題の一つになり、ステンレス鋼は適用されてこなかった。 Stainless steel is a material with excellent corrosion resistance, and martensitic SUS410 series materials are widely used for motorcycles and other two-wheeled vehicles. This is because the disc rotor of a two-wheeled vehicle is exposed and easily visible, and corrosion resistance is emphasized. On the other hand, stainless steel has a problem that its thermal conductivity is inferior to that of cast iron. In motorcycles, the brake system is exposed, and stainless steel is used without problems because of its excellent cooling performance. In the case of automobiles, the brake system, including the tires, is housed in the tire house, so the disc rotor is difficult to cool, and one of the issues is low thermal conductivity, which is why stainless steel has not been applied.
ところが近年のEV、FCV、HV車などでは、走行時の運動エネルギーを電気エネルギーに変換し回収する「回生ブレーキ」の採用が急激に伸びている。この適用により、ディスクローターとパッドの摩擦で生じていた摩擦熱が低減するため、鋳鉄よりも熱伝導率が劣るステンレス鋼にも適用の可能性が広がっている。 However, in recent years, EVs, FCVs, HVs, etc. have rapidly adopted "regenerative braking" that converts and recovers kinetic energy during running into electrical energy. Since this application reduces the frictional heat generated by the friction between the disc rotor and the pad, the possibility of application to stainless steel, which is inferior to cast iron in thermal conductivity, is expanding.
自動車のディスクブレーキへのステンレス鋼の適用を妨げていたもう一つの課題は成形性である。二輪車のディスクローターはリング状の円盤形で、板状のステンレス鋼から打ち抜き加工して製造されるため大きな加工はない。一方、現状の自動車のディスクローターは、ハット形状と呼ばれる、円盤の中央を絞ったような形状であり、鋳造によって製造されている。このような形状のものを、ステンレス鋼を加工して成形するには深絞り加工が必要となる。ただし二輪車で用いられてきたステンレス鋼はマルテンサイト系ステンレス鋼であり、非常に硬度が高くその加工が困難であった。これを解決する一つの方法として、高温でプレス加工するホットスタンプが近年広まっている。これによりステンレス鋼も精度よくハット形状を成形できるようになった。 Another issue that has hampered the application of stainless steels in automotive disc brakes is formability. A disc rotor for a motorcycle is a ring-shaped disc, and is manufactured by punching from a plate-shaped stainless steel, so there is no need for large processing. On the other hand, the disk rotors of current automobiles have a shape called a hat shape, which looks like a disk whose center is squeezed, and are manufactured by casting. Deep drawing is required to process stainless steel into such a shape. However, the stainless steel that has been used for motorcycles is martensitic stainless steel, which is extremely hard and difficult to process. As one method for solving this problem, hot stamping, which is a method of pressing at a high temperature, has been widely used in recent years. This made it possible to mold stainless steel into a hat shape with high accuracy.
こうした背景のなか、近年の燃費向上の要請に対応するためには、ディスクローターの薄肉軽量化が必要となる。しかし鋳鉄は強度が低く、また鋳造で作製されるために薄肉化に限界がある。加えて自動車のブレーキ時の到達温度は最大で700℃近傍に達すると言われており、耐熱温度が500℃近傍であるマルテンサイト系ステンレス鋼では適用が難しい場合がある。また山道などのブレーキを多用する走行条件における到達温度は300℃になる場合がある。 Against this background, it is necessary to reduce the thickness and weight of disc rotors in order to meet the recent demand for improved fuel efficiency. However, cast iron has low strength and is manufactured by casting, so there is a limit to how thin it can be made. In addition, it is said that the maximum temperature reached during braking of an automobile reaches around 700°C, and it may be difficult to apply it to martensitic stainless steel, which has a heat resistance temperature of around 500°C. In some cases, the temperature reaches 300° C. under driving conditions such as mountain roads where brakes are frequently used.
自動車のステンレス鋼製ディスクローターに関して特許文献1があるが、主として成形性に着目しており、高温強度には着目していない。また、特許文献2では高飽和の固溶C、Nを活用したマルテンサイト相で強度を向上させているが、700℃近傍の強度に関しては言及されていない。また、いずれの特許文献もマルテンサイト組織を活用したものであり、700℃近傍における耐熱性を確保できるものは見当たらない。 There is Patent Document 1 regarding stainless steel disk rotors for automobiles, but it focuses mainly on formability, not on high-temperature strength. Further, in Patent Document 2, strength is improved by a martensite phase utilizing highly saturated solute C and N, but strength around 700° C. is not mentioned. Moreover, all of the patent documents utilize the martensite structure, and none of them can ensure heat resistance in the vicinity of 700°C.
本発明は、耐熱性と成形性に優れた自動車ブレーキディスクローター用フェライト系ステンレス鋼板に関するものである。本発明の解決しようとする課題の対象となる部品は、自動車の制動系部品、特にディスクローターである。
自動車のディスクローターはハット形状であるため、成形性が要求される。また到達温度は一般的な市街地走行では100℃程度、山道の走行では300℃程度、最大では700℃近傍に達するため、薄肉化のためには中温域~高温域における強度が要求される。鋳鉄は鋳造によって成型されるため、ディスクローターを薄肉化すると湯流れが悪くなり、成型できない場合がある。また、強度が低いため薄肉化を行うとディスクローターとして十分な強度を確保できない問題があった。フェライト系ステンレス鋼はホットスタンプを行うことで精度よくハット形状を成形できる。ただし、強度が低いステンレス鋼では薄肉化を行うことができない。一方、強度が高いステンレス鋼ではホットスタンプ時に過大な荷重が必要となり、精度よくハット形状に成形を行うことができない、もしくは割れが生じる可能性がある。また、マルテンサイト系ステンレス鋼はホットスタンプによる成形性に優れるが、耐熱温度は500℃程度であり、成形性と耐熱性を両立できない。TECHNICAL FIELD The present invention relates to a ferritic stainless steel sheet for automobile brake disc rotors, which is excellent in heat resistance and formability. The parts to be solved by the present invention are braking system parts of automobiles, particularly disc rotors.
Since the disk rotor of an automobile is shaped like a hat, formability is required. In addition, the temperature reached is about 100°C in general urban driving, about 300°C in mountain road driving, and reaches about 700°C at maximum, so strength in the medium to high temperature range is required for thinning. Since cast iron is formed by casting, if the disk rotor is made thin, the flow of molten metal will be poor and it may not be possible to form it. In addition, since the strength is low, if the thickness is reduced, there is a problem that sufficient strength cannot be secured as a disc rotor. Ferritic stainless steel can be formed into a hat shape with high accuracy by hot stamping. However, stainless steel, which has low strength, cannot be thinned. On the other hand, stainless steel, which has high strength, requires an excessive load during hot stamping, and it may not be possible to form it into a hat shape with high accuracy, or cracks may occur. Also, martensitic stainless steel is excellent in formability by hot stamping, but its heat resistance temperature is about 500° C., and both formability and heat resistance cannot be achieved.
本発明は高温強度に優れ、優れた成形性を有する、自動車ブレーキディスクローター用フェライト系ステンレス鋼板、自動車ブレーキディスクローター及び自動車ブレーキディスクローター用ホットスタンプ加工品を提供するものである。 The present invention provides a ferritic stainless steel sheet for automobile brake disc rotors, an automobile brake disc rotor, and a hot-stamped product for automobile brake disc rotors, which have excellent high-temperature strength and excellent formability.
上記課題を解決するために、本発明者らはフェライト系ステンレス鋼板の析出物に着目して詳細に調査した。前記本発明が対象とする部品がホットスタンプにて成形される温度域では、鋼中に析出物が析出する場合がある。析出物は微細に分散させれば、材料の強度を向上させることができる。しかし、成形前に析出物が存在すると強度が高くなりすぎ、鋼の伸びが低下することで成形時に割れが発生する可能性がある。そこで、ホットスタンプ時に析出物が微細に析出することで、成形性と成形後の強度を確保できると考えた。そして、かかる目的を達成すべく種々の検討を重ねた結果、以下の知見を得た。 In order to solve the above problems, the present inventors paid attention to the precipitates on the ferritic stainless steel sheet and investigated them in detail. In the temperature range in which the parts targeted by the present invention are formed by hot stamping, precipitates may occur in the steel. Finely dispersed precipitates can improve the strength of the material. However, the presence of precipitates prior to forming can lead to excessive strength and reduced elongation of the steel, which can lead to cracking during forming. Therefore, it was thought that the formability and the strength after forming could be ensured by forming fine precipitates during hot stamping. As a result of various investigations aimed at achieving this object, the following findings were obtained.
Si添加量を適切に制御し、かつ熱延後の仕上げ温度を900~1100℃にし、巻き取り温度を650℃以下にすることで、ホットスタンプ時の加熱の際に結晶粒径を大きくし、ホットスタンプ中に析出物を析出させる。さらに仕上げ温度を950℃超にすることで結晶粒径を効果的に大きくし、中温域の強度も向上させる。析出物は鋼の結晶粒内に微細析出するため、ディスクローターとして使用中に優れた高温強度を得ることができる。結晶粒界に析出する析出物は成長・粗大化しやすい。これに対し、ホットスタンプ時の加熱の際に、結晶粒径を適切に制御することによって析出物が主として結晶粒内に析出することを知見した。結晶粒内の析出物は結晶粒界の析出物よりも成長しにくく使用中の粗大化が生じにくい。析出物がホットスタンプ中に粒内に微細に析出することによって析出強化が効果的に発現する。これにより、ディスクローターに適用可能な耐熱フェライト系ステンレス鋼板を提供することに成功した。 The amount of Si added is appropriately controlled, the finishing temperature after hot rolling is 900 to 1100 ° C., and the winding temperature is 650 ° C. or less, so that the crystal grain size is increased during heating during hot stamping, Precipitates are deposited during hot stamping. Furthermore, by setting the finishing temperature to over 950° C., the crystal grain size is effectively increased, and the strength in the intermediate temperature range is also improved. Since the precipitates are finely precipitated within the crystal grains of the steel, excellent high-temperature strength can be obtained during use as a disc rotor. Precipitates that precipitate at grain boundaries tend to grow and coarsen. On the other hand, it has been found that the precipitates are mainly precipitated in the crystal grains by appropriately controlling the crystal grain size during heating during hot stamping. Precipitates within grains are less likely to grow and coarsen during use than precipitates at grain boundaries. Precipitation strengthening is effectively achieved by the fine precipitation of precipitates within grains during hot stamping. As a result, we have succeeded in providing a heat-resistant ferritic stainless steel sheet that can be applied to disk rotors.
上記課題を解決する本発明の要旨は以下のとおりである。
[1]質量%にて、C:0.001~0.05%、N:0.001~0.05%、Si:0.3~4.0%、Mn:0.01~2.0%、P:0.01~0.05%、S:0.0001~0.02%、Cr:10~20%、を含有し、さらにTi:0.001~0.5%、Nb:0.01~0.8%を1種または2種含有し、残部がFeおよび不純物であり、
1000℃まで加熱し、その後890~700℃で1分以上10分以下滞留する冷却をする熱処理(以下「ホットスタンプ疑似熱処理」という。)を行ったとき、結晶粒径が100~200μmとなり、粒径500nm以下の析出物が0.01~20個/μm2の密度となる、ホットスタンプ加工用であることを特徴とする自動車ブレーキディスクローター用フェライト系ステンレス鋼板。The gist of the present invention for solving the above problems is as follows.
[1] In mass%, C: 0.001 to 0.05%, N: 0.001 to 0.05%, Si: 0.3 to 4.0%, Mn: 0.01 to 2.0 %, P: 0.01 to 0.05%, S: 0.0001 to 0.02%, Cr: 10 to 20%, Ti: 0.001 to 0.5%, Nb: 0 .01 to 0.8% containing one or two types, the balance being Fe and impurities,
Heating to 1000 ° C., and then heat treatment (hereinafter referred to as “hot stamping pseudo heat treatment”) in which cooling is performed by staying at 890 to 700 ° C. for 1 minute or more and 10 minutes or less. A ferritic stainless steel sheet for automobile brake disc rotors, characterized by having a density of 0.01 to 20/μm 2 of precipitates with a diameter of 500 nm or less, which is for hot stamping.
[2]質量%にて、C:0.001~0.05%、N:0.001~0.05%、Si:0.3~4.0%、Mn:0.01~2.0%、P:0.01~0.05%、S:0.0001~0.02%、Cr:10~20%、を含有し、さらにTi:0.001~0.5%、Nb:0.01~0.8%を1種または2種含有し、残部がFeおよび不純物であり、
結晶粒径が100~200μmであり、粒径500nm以下の析出物が0.01~20個/μm2の密度で存在する、ホットスタンプ加工品を構成する自動車ブレーキディスクローター用フェライト系ステンレス鋼板。[2] In mass%, C: 0.001 to 0.05%, N: 0.001 to 0.05%, Si: 0.3 to 4.0%, Mn: 0.01 to 2.0 %, P: 0.01 to 0.05%, S: 0.0001 to 0.02%, Cr: 10 to 20%, Ti: 0.001 to 0.5%, Nb: 0 .01 to 0.8% containing one or two types, the balance being Fe and impurities,
A ferritic stainless steel sheet for automobile brake disc rotors constituting a hot-stamped product having a grain size of 100 to 200 μm and precipitates having a grain size of 500 nm or less at a density of 0.01 to 20/μm 2 .
[3]質量%にて、C:0.001~0.05%、N:0.001~0.05%、Si:0.3~4.0%、Mn:0.01~2.0%、P:0.01~0.05%、S:0.0001~0.02%、Cr:10~20%を含有し、さらにTi:0.001~0.5%、Nb:0.01~0.8%を1種または2種を含有し、残部がFeおよび不純物である自動車ブレーキディスクローター用フェライト系ステンレス鋼板。 [3] In mass%, C: 0.001 to 0.05%, N: 0.001 to 0.05%, Si: 0.3 to 4.0%, Mn: 0.01 to 2.0 %, P: 0.01-0.05%, S: 0.0001-0.02%, Cr: 10-20%, Ti: 0.001-0.5%, Nb: 0.001-0.5%. A ferritic stainless steel sheet for automobile brake disc rotors containing 01 to 0.8% of 1 or 2 and the balance being Fe and impurities.
[4]ホットスタンプ加工用であることを特徴とする本発明の自動車ブレーキディスクローター用フェライト系ステンレス鋼板。
[5]1000℃における破断伸びが50%以上であり、前記ホットスタンプ疑似熱処理後において、700℃における0.2%耐力が80MPa以上であることを特徴とする本発明の自動車ブレーキディスクローター用フェライト系ステンレス鋼板。
[6]700℃における0.2%耐力が80MPa以上であることを特徴とする本発明の自動車ブレーキディスクローター用フェライト系ステンレス鋼板。
[7]前記結晶粒径が130~200μmである本発明の自動車ブレーキディスクローター用フェライト系ステンレス鋼板。
[8]1000℃における破断伸びが50%以上であることを特徴とする本発明の自動車ブレーキディスクローター用フェライト系ステンレス鋼板。
[9]300℃における0.2%耐力が170MPa以上であることを特徴とする本発明の自動車ブレーキディスクローター用フェライト系ステンレス鋼板。[4] A ferritic stainless steel sheet for automobile brake disc rotors according to the present invention, which is for hot stamping.
[5] The ferrite for automobile brake disc rotors of the present invention, which has an elongation at break of 50% or more at 1000°C and a 0.2% proof stress at 700°C of 80 MPa or more after the hot stamping pseudo heat treatment. system stainless steel plate.
[6] A ferritic stainless steel sheet for automobile brake disc rotors according to the present invention, which has a 0.2% proof stress of 80 MPa or more at 700°C.
[7] The ferritic stainless steel sheet for automobile brake disc rotors according to the present invention, wherein the crystal grain size is 130 to 200 μm.
[8] A ferritic stainless steel sheet for automobile brake disc rotors according to the present invention, which has an elongation at break of 50% or more at 1000°C.
[9] A ferritic stainless steel sheet for automobile brake disc rotors according to the present invention, which has a 0.2% proof stress of 170 MPa or more at 300°C.
[10]前記Feの一部に替えて、質量%にてさらに、B:0.0001~0.0030%、Al:0.001~4.0%、Cu:0.01~3.0%、Mo:0.01~3.0%、W:0.001~2.0%、V:0.001~1.0%、Sn:0.01~0.5%、Ni:0.01~1.0%、Mg:0.0001~0.01%、Sb:0.005~0.5%、Zr:0.001~0.3%、Ta:0.001~0.3%、Hf:0.001~0.3%、Co:0.001~0.3%、Ca:0.0001~0.01%、REM:0.001~0.2%、Ga:0.0002~0.3%の1種以上を含有することを特徴とする本発明の自動車ブレーキディスクローター用フェライト系ステンレス鋼板。 [10] In place of part of the Fe, B: 0.0001 to 0.0030%, Al: 0.001 to 4.0%, Cu: 0.01 to 3.0% in mass% , Mo: 0.01 to 3.0%, W: 0.001 to 2.0%, V: 0.001 to 1.0%, Sn: 0.01 to 0.5%, Ni: 0.01 ~1.0%, Mg: 0.0001-0.01%, Sb: 0.005-0.5%, Zr: 0.001-0.3%, Ta: 0.001-0.3%, Hf: 0.001-0.3%, Co: 0.001-0.3%, Ca: 0.0001-0.01%, REM: 0.001-0.2%, Ga: 0.0002- 0.3% of one or more ferritic stainless steel sheets for automobile brake disc rotors according to the present invention.
[11]本発明のステンレス鋼板を用いてなる自動車ブレーキディスクローター。
[12]本発明のステンレス鋼板を用いてなる自動車ブレーキディスクローター用ホットスタンプ加工品。[11] An automobile brake disc rotor using the stainless steel sheet of the present invention.
[12] A hot-stamped article for automobile brake disc rotors, which uses the stainless steel sheet of the present invention.
本発明によればフェライト系ステンレス鋼板の耐熱性と成形性を向上させ、自動車ブレーキディスクローターに適した材料を提供し、軽量化や美観の改善などに大きな効果が得られる。 According to the present invention, it is possible to improve the heat resistance and formability of ferritic stainless steel sheets, provide materials suitable for automobile brake disc rotors, and achieve significant effects such as weight reduction and aesthetic improvement.
フェライト系ステンレス鋼板を用い、ホットスタンプ加工によって自動車ブレーキディスクローターを製造するに際し、鋼板を1000℃前後に加熱してホットスタンプ加工を行う。ホットスタンプ加工前の鋼板は、1000℃前後で行うホットスタンプ加工で十分な延性を有していることが要求される。一方、ホットスタンプ後の自動車ブレーキディスクローターについては、十分な高温強度を実現することが必要である。 When manufacturing an automobile brake disc rotor by hot stamping using a ferritic stainless steel sheet, the steel sheet is heated to around 1000° C. and hot stamped. A steel sheet before hot stamping is required to have sufficient ductility in hot stamping performed at around 1000°C. On the other hand, for automobile brake disc rotors after hot stamping, it is necessary to achieve sufficient high-temperature strength.
前述のように、ホットスタンプにて成形される温度域では、析出物が析出する場合がある。鋼中に析出物を微細に分散させれば、材料の強度を向上させることができる。しかし、成形前に析出物が存在すると強度が高くなりすぎ、伸びが低下することでホットスタンプ成形時に割れが発生する可能性がある。そこで本発明は、ホットスタンプ時に析出物が微細に析出することで、ホットスタンプ成形性と、成形後の強度を確保する。 As described above, precipitates may form in the hot stamping temperature range. Finely dispersed precipitates in steel can improve the strength of the material. However, the presence of precipitates prior to forming may result in excessive strength and reduced elongation, which may lead to cracking during hot stamping. Therefore, the present invention secures hot stamping moldability and strength after molding by finely depositing precipitates during hot stamping.
ホットスタンプ中における鋼の結晶粒径に着目する。結晶粒径が小さい場合、鋼中に結晶粒界の占める比率が高いため、ホットスタンプ中において結晶粒界への析出が多くなる。結晶粒界に析出する析出物は成長・粗大化しやすく、微細析出物が得にくくなる。本発明は、ホットスタンプ時の加熱の際に、結晶粒径を成長させて適切に制御することによって、析出物が主として粒内に析出することを知見した。粒内の析出物は粒界の析出物よりも成長しにくく使用中の粗大化が生じにくい。析出物がホットスタンプ中に粒内に微細に析出することによって、ホットスタンプ後に析出強化が効果的に発現し、成形後の強度を確保する。 We focus on the grain size of steel during hot stamping. When the crystal grain size is small, the ratio of crystal grain boundaries in the steel is high, so precipitation at the crystal grain boundaries increases during hot stamping. Precipitates that precipitate at grain boundaries tend to grow and coarsen, making it difficult to obtain fine precipitates. In the present invention, it has been found that the precipitates are mainly precipitated in the grains by growing the crystal grain size and appropriately controlling it during heating during hot stamping. Intragranular precipitates grow more slowly than grain boundary precipitates and are less likely to coarsen during use. Precipitation strengthening occurs effectively after hot stamping and secures strength after forming by fine precipitation of precipitates in grains during hot stamping.
以上のように、本発明ではホットスタンプ後において高温強度の観点から粒内に析出物が微細に析出することが重要であり、そのためにはホットスタンプ時の加熱の際における結晶粒径をある程度成長させる必要があることを知見した。具体的には、ホットスタンプ後における結晶粒径を100~200μmとすることにより、析出物の微細化を実現できることが判明した。なお、ホットスタンプ時における結晶粒径はホットスタンプ後の結晶粒径と同じであることがわかっている。このような結晶粒径範囲であれば、析出する析出物は粒内に微細析出し、かつ、成長しにくく、これらは対応関係があると推定される。
そこで本発明においては、ホットスタンプ後における結晶粒径で金属組織を規定することとした。ホットスタンプ後における結晶粒径を100~200μmに制御することによって、ホットスタンプ中に析出物は微細析出し、かつ、成長しにくく、析出強化が効果的に発現する。ホットスタンプ後の結晶粒径が100μm以上であれば、析出物が微細析出し、700℃近傍までの十分な耐力を得られた。さらに、ホットスタンプ後の結晶粒径が130μm以上であれば、300℃近傍の中温域においても十分な耐力を得られた。As described above, in the present invention, it is important from the viewpoint of high-temperature strength after hot stamping that the precipitates are finely precipitated in the grains. I found that I needed to. Specifically, it has been found that by setting the crystal grain size to 100 to 200 μm after hot stamping, the refinement of precipitates can be realized. It is known that the crystal grain size during hot stamping is the same as the crystal grain size after hot stamping. In such a crystal grain size range, the deposited precipitates are finely precipitated in the grains and are difficult to grow, and it is presumed that there is a corresponding relationship between them.
Therefore, in the present invention, the metal structure is defined by the crystal grain size after hot stamping. By controlling the crystal grain size after hot stamping to 100 to 200 μm, precipitates are finely precipitated during hot stamping and are difficult to grow, so that precipitation strengthening is effectively exhibited. When the crystal grain size after hot stamping was 100 μm or more, fine precipitates were formed, and sufficient yield strength up to around 700° C. was obtained. Furthermore, when the crystal grain size after hot stamping is 130 μm or more, a sufficient yield strength was obtained even in a medium temperature range around 300°C.
鋼中の結晶粒は、ホットスタンプでの加熱によって成長し、結晶粒径が増大する。ホットスタンプ前の結晶粒径が大きいほど、ホットスタンプ中及びホットスタンプ後の結晶粒径も大きくなる傾向にある。ホットスタンプ後の結晶粒径が200μmを超える場合は、ホットスタンプ前の鋼板の結晶粒径も大きくなっている場合であり、その結果として鋼板の靭性が著しく低下することになる。そのため、ホットスタンプ後における結晶粒径の上限は200μmとした。 Crystal grains in steel grow by heating with a hot stamp, increasing the grain size. There is a tendency that the larger the crystal grain size before hot stamping, the larger the crystal grain size during and after hot stamping. If the crystal grain size after hot stamping exceeds 200 μm, the crystal grain size of the steel sheet before hot stamping is also large, and as a result, the toughness of the steel sheet is remarkably lowered. Therefore, the upper limit of the crystal grain size after hot stamping was set to 200 μm.
また、ホットスタンプ後において析出強化を効果的に発現させるため、ホットスタンプ後の鋼中に、粒径500nm以下の析出物が0.01~20個/μm2の密度で存在することと規定する。粒径500nm以下の析出物が0.01~20個/μm2の密度で存在することによって、700℃近傍まで十分な耐力を得られる。粒径が500nmを超えると析出強化が作用しにくくなる。また析出物密度が0.01個/μm2未満であると析出量が少ないために析出強化が作用しにくい。20個/μm2超であると強度が過度に上昇し、割れが生じやすくなる。上記より粒内の析出物は、粒径500nm以下の析出物が0.01~20個/μm2の密度で存在することが望ましい。In addition, in order to effectively develop precipitation strengthening after hot stamping, it is specified that precipitates with a grain size of 500 nm or less exist in the steel after hot stamping at a density of 0.01 to 20 / μm 2 . . Precipitates having a grain size of 500 nm or less are present at a density of 0.01 to 20/μm 2 , so that a sufficient yield strength can be obtained up to around 700°C. If the grain size exceeds 500 nm, precipitation strengthening becomes difficult to act. If the density of precipitates is less than 0.01/μm 2 , the amount of precipitates is so small that precipitation strengthening is difficult to act. If it exceeds 20 pieces/μm 2 , the strength increases excessively and cracks are likely to occur. From the above, it is desirable that precipitates having a particle size of 500 nm or less exist in the grains at a density of 0.01 to 20/μm 2 .
評価対象品がホットスタンプ加工品、あるいは最終製品である自動車ブレーキディスクローターであれば、鋼中の結晶粒径及び析出物密度の評価を行うことができる。一方、評価対象品がホットスタンプ加工前の鋼板である場合、当該鋼板にホットスタンプ疑似熱処理を施し、その上で鋼中の結晶粒径及び析出物密度の評価を行うこととすればよい。ホットスタンプ疑似熱処理としては、1000℃まで加熱し、その後890~700℃で1分以上10分以下、例えば2分間滞留する冷却を行う熱処理とすればよい。 If the product to be evaluated is a hot-stamped product or an automobile brake disc rotor, which is the final product, the crystal grain size and precipitate density in steel can be evaluated. On the other hand, when the product to be evaluated is a steel plate before hot stamping, the steel plate is subjected to hot stamping pseudo heat treatment, and then the grain size and precipitate density in the steel are evaluated. As the hot stamping pseudo heat treatment, heat treatment may be performed by heating to 1000° C. and then cooling at 890 to 700° C. for 1 minute or more and 10 minutes or less, for example, 2 minutes.
以下、鋼中の成分含有量を規定した根拠について説明する。
Cは、成形性と耐食性を劣化させ、鋼板の高温伸び及び高温強度の低下をもたらすとともに、ホットスタンプ後にCr炭窒化物、Nb炭窒化物の析出によって析出物密度が過剰となるため、その含有量は少ないほど良い。そのため、0.05%以下とした。0.020%以下が望ましい。さらに望ましくは0.0015%以下とする。但し、過度の低減は精錬コストの増加に繋がるため、0.001%以上とすると好ましい。The grounds for specifying the content of ingredients in steel will be described below.
C degrades formability and corrosion resistance, lowers the high-temperature elongation and high-temperature strength of the steel sheet, and causes excessive precipitate density due to the precipitation of Cr carbonitrides and Nb carbonitrides after hot stamping. The less the amount, the better. Therefore, it is set to 0.05% or less. 0.020% or less is desirable. More desirably, the content is 0.0015% or less. However, excessive reduction leads to an increase in refining cost, so it is preferable to make it 0.001% or more.
NはCと同様、成形性と耐食性を劣化させ、鋼板の高温伸び及び高温強度の低下をもたらすとともに、ホットスタンプ後にCr炭窒化物、Nb炭窒化物の析出によって析出物密度が過剰となるため、その含有量は少ないほど良い。そのため、0.05%以下とした。0.020%以下が望ましい。さらに望ましくは0.015%以下とする。但し、過度の低減は精錬コストの増加に繋がるため、0.001%以上とすると好ましい。 Like C, N degrades formability and corrosion resistance, lowers the high-temperature elongation and high-temperature strength of the steel sheet, and precipitates Cr carbonitrides and Nb carbonitrides after hot stamping, resulting in an excessive precipitate density. , the lower the content, the better. Therefore, it is set to 0.05% or less. 0.020% or less is desirable. More desirably, the content is 0.015% or less. However, excessive reduction leads to an increase in refining cost, so it is preferable to make it 0.001% or more.
Siは、脱酸剤としても有用な元素であるとともに、高温強度、耐酸化性および耐高温塩害性を改善する元素である。高温強度、耐酸化性および耐高温塩害性は、Si量の増加とともに向上する。高温強度の向上には析出の制御が重要であり、析出物を微細かつ多量に析出させることで、その効果を得られる。Siには時効中の析出物を微細に析出させる作用があり、その効果は、0.3%から安定して発現する。しかしながら、Siの過度な添加は鋼板での常温及び高温での延性を低下させ、熱延板が硬質化して靱性が低下するとともに、結晶粒径が微細化しかつホットスタンプ中の析出物生成が過剰となるため、その上限を4.0%とする。また、酸洗性や靭性を考慮すると0.3%以上が望ましく、3.5%以下が望ましい。さらに製造性を考慮すると3.0%以下が望ましい。 Si is an element that is also useful as a deoxidizing agent, and is an element that improves high-temperature strength, oxidation resistance, and high-temperature salt damage resistance. High-temperature strength, oxidation resistance, and high-temperature salt damage resistance improve as the amount of Si increases. Precipitation control is important for improving high-temperature strength, and the effect can be obtained by precipitating a large amount of fine precipitates. Si has the effect of finely precipitating precipitates during aging, and the effect is stably exhibited from 0.3%. However, excessive addition of Si reduces the ductility of the steel sheet at room temperature and high temperature, hardens the hot-rolled sheet and reduces toughness, refines the grain size, and excessively generates precipitates during hot stamping. Therefore, the upper limit is set to 4.0%. Also, considering the pickling property and toughness, it is preferably 0.3% or more, and preferably 3.5% or less. Furthermore, considering manufacturability, 3.0% or less is desirable.
Mnは、脱酸剤として添加される元素であるとともに、中温域での高温強度上昇に寄与するが、2.0%超の添加により、強化に寄与しないMnSが多量に析出して疑似熱処理後の高温強度が低下するとともに、高温でMn系酸化物を表層に形成し、スケール密着性不良や異常酸化が生じ易くなる。特に、MoやWと共に複合添加した場合は、Mn量に対して異常酸化が生じやすくなる傾向にある。そのため、上限を2.0%とした。更に、鋼板製造における酸洗性や常温延性を考慮すると、0.01%以上が望ましく、1.5%以下が望ましい。さらに望ましくは1.0%以下とする。 Mn is an element added as a deoxidizing agent and contributes to an increase in high-temperature strength in the medium temperature range. At the same time, Mn-based oxides are formed on the surface layer at high temperatures, resulting in poor scale adhesion and abnormal oxidation. In particular, when Mo and W are added together, abnormal oxidation tends to occur more easily with respect to the amount of Mn. Therefore, the upper limit was made 2.0%. Furthermore, considering the pickling property and room temperature ductility in steel plate production, the content is preferably 0.01% or more and 1.5% or less. More desirably, the content is 1.0% or less.
Pは、製鋼精錬時に主として原料から混入してくる不純物であり、含有量が高くなると、鋼板の靭性や溶接性が低下する。このため、極力低減することが望ましいが、0.01%未満にするためには、低P原料の使用によるコストアップが生じるため、本発明では0.01%以上とする。さらに望ましくは0.02%以上とする。一方、0.05%超の含有により著しく硬質化する他、耐食性、靭性および酸洗性が劣化するため、0.05%を上限とする。さらに望ましくは0.04%以下とする。 P is an impurity mainly mixed from raw materials during steelmaking refining, and when the content is high, the toughness and weldability of the steel sheet are lowered. For this reason, it is desirable to reduce the P content as much as possible. However, in order to reduce the P content to less than 0.01%, the cost increases due to the use of low-P raw materials. More desirably, it should be 0.02% or more. On the other hand, if the content exceeds 0.05%, the hardness is significantly increased, and the corrosion resistance, toughness, and pickling properties are deteriorated. More desirably, the content is 0.04% or less.
Sは、耐食性や耐酸化性を劣化させる元素であるが、TiやCと結合して加工性を向上させる効果が0.0001%から発現するため、下限を0.0001%とした。更に、精錬コストを考慮すると0.0010%以上が望ましい。一方、過度な添加によりTiやCと結合して固溶Ti量を低減させるとともに析出物の粗大化をもたらし、鋼板の靱性や高温強度が低下するため、上限を0.02%とした。更に、高温酸化特性を考慮すると0.0090%以下が望ましい。 S is an element that deteriorates corrosion resistance and oxidation resistance, but the effect of improving workability by combining with Ti and C appears from 0.0001%, so the lower limit was made 0.0001%. Furthermore, considering refining cost, 0.0010% or more is desirable. On the other hand, excessive addition combines with Ti and C to reduce the amount of solid solution Ti and cause precipitates to coarsen, which lowers the toughness and high-temperature strength of the steel sheet, so the upper limit was made 0.02%. Furthermore, considering high-temperature oxidation characteristics, 0.0090% or less is desirable.
Crは、本発明において、耐酸化性や耐食性確保のために必須な元素である。10%未満では、特に耐酸化性が確保できず、さらにホットスタンプ後の700℃耐力が低下するとともに、結晶粒径の増大をもたらす。一方、20%超では加工性の低下や靭性の劣化をもたらすとともに、ホットスタンプ後の析出物数が過大となるため、10~20%とした。更に、製造性やスケール剥離性を考慮すると12%以上が望ましく、18%以下が望ましい。さらに望ましくは15%以下とする。 Cr is an essential element for securing oxidation resistance and corrosion resistance in the present invention. If it is less than 10%, the oxidation resistance cannot be ensured, the 700° C. proof stress after hot stamping is lowered, and the crystal grain size is increased. On the other hand, if it exceeds 20%, workability and toughness are deteriorated, and the number of precipitates after hot stamping becomes excessive. Furthermore, considering manufacturability and scale removability, the content is preferably 12% or more, and preferably 18% or less. More desirably, it is 15% or less.
Ti:0.001~0.5%、Nb:0.01~0.8%を1種または2種含有する。
Tiは、C,N,Sと結合して耐食性、耐粒界腐食性、常温延性や深絞り性を向上させる元素である。また、必要に応じて添加する。また、Nb、Moとの複合添加において、適量添加することにより、熱延焼鈍時のNb、Moの固溶量増加、高温強度の向上をもたらし、熱疲労特性を向上させる。その効果は0.001%以上から発現するため、下限を0.001%とした。一方、0.5%超の添加により、固溶Ti量が増加して鋼板での常温及び高温の延性が低下する他、ホットスタンプ後の析出物数が過剰となり、さらに粗大なTi系析出物を形成し、穴拡げ加工時の割れの起点になり、プレス加工性を劣化させる。また、耐酸化性も劣化するため、Ti添加量は0.5%以下とした。更に、表面疵の発生や靭性を考慮すると0.05%以上が望ましく、0.2%以下が望ましい。One or two of Ti: 0.001 to 0.5% and Nb: 0.01 to 0.8% are contained.
Ti is an element that combines with C, N and S to improve corrosion resistance, intergranular corrosion resistance, room temperature ductility and deep drawability. Moreover, it adds as needed. Further, in the combined addition of Nb and Mo, by adding an appropriate amount, the solid solution amount of Nb and Mo during hot rolling annealing is increased, the high-temperature strength is improved, and the thermal fatigue characteristics are improved. Since the effect is exhibited from 0.001% or more, the lower limit was made 0.001%. On the other hand, if the addition exceeds 0.5%, the amount of solid solution Ti increases and the ductility of the steel sheet at room temperature and high temperature decreases, and the number of precipitates after hot stamping becomes excessive, and further coarse Ti-based precipitates. It becomes the starting point of cracks during hole expansion and deteriorates press workability. In addition, the amount of Ti added is set to 0.5% or less because the oxidation resistance is also deteriorated. Furthermore, considering the occurrence of surface flaws and toughness, the content is preferably 0.05% or more, and is preferably 0.2% or less.
Nbは、固溶強化および微細析出物の析出強化による高温強度向上に有効な元素である。また、CやNを炭窒化物として固定し、製品板の耐食性やr値に影響する再結晶集合組織の発達に寄与する役割もある。これらの効果は0.01%から発現するため、下限を0.01%とした。一方、0.8%超の添加は、鋼板での高温延性が低下するとともに、ホットスタンプ後の析出物数が過剰となり、さらに著しく硬質化する他、製造性も劣化させるため、上限を0.8%とした。また、原料コストや靭性を考慮すると、0.3%以上が望ましく、0.6%以下が望ましい。 Nb is an element effective in improving high-temperature strength through solid-solution strengthening and precipitation strengthening of fine precipitates. It also has the role of fixing C and N as carbonitrides and contributing to the development of the recrystallized texture that affects the corrosion resistance and r-value of the product sheet. Since these effects appear from 0.01%, the lower limit was made 0.01%. On the other hand, addition of more than 0.8% lowers the high-temperature ductility of the steel sheet, and the number of precipitates after hot stamping becomes excessive, resulting in significant hardening and deterioration of manufacturability. 8%. Moreover, considering raw material cost and toughness, 0.3% or more is desirable, and 0.6% or less is desirable.
鋼中の成分として、上記組成の他、残部がFeおよび不純物である。本発明は、さらに必要に応じて、前記Feの一部に替えて、以下の成分を含有することとしても良い。 As components in the steel, the balance is Fe and impurities in addition to the above composition. The present invention may further contain the following components instead of part of the Fe, if necessary.
Bは、製品のプレス加工時の2次加工性や高温強度、熱疲労特性を向上させる元素である。BはLaves相などの微細析出をもたらし、これらの析出強化の長期安定性を発現させ、強度低下の抑制や熱疲労寿命の向上に寄与する。この効果は0.0001%以上で発現する。一方、過度な添加は硬質化をもたらし、粒界腐食性と耐酸化性を劣化させる他、溶接割れが生じるため、0.0030%以下とした。更に、耐食性や製造コストを考慮すると、0.0010%以下が望ましい。さらに望ましくは0.0005%以下とする。 B is an element that improves secondary workability, high-temperature strength, and thermal fatigue properties during press working of the product. B brings about fine precipitations such as Laves phases, develops long-term stability of these precipitation strengthening, and contributes to suppression of strength reduction and improvement of thermal fatigue life. This effect is expressed at 0.0001% or more. On the other hand, excessive addition causes hardening, degrades intergranular corrosion resistance and oxidation resistance, and causes weld cracking. Furthermore, considering corrosion resistance and manufacturing cost, 0.0010% or less is desirable. More desirably, the content is 0.0005% or less.
Alは、脱酸元素として添加される他、耐酸化性を向上させる元素である。また、固溶強化元素として高温強度向上に有用である。その作用は0.001%から安定して発現する。一方、過度の添加は鋼を硬質化して均一伸びを著しく低下させる他、靭性が著しく低下するため、上限を4.0%とした。更に、表面疵の発生や溶接性、製造性を考慮すると、0.01%以上が望ましく、2.2%以下が望ましい。 Al is an element that is added as a deoxidizing element and also improves oxidation resistance. In addition, it is useful as a solid-solution strengthening element for improving high-temperature strength. Its action is stably expressed from 0.001%. On the other hand, excessive addition hardens the steel and significantly lowers the uniform elongation and toughness, so the upper limit was made 4.0%. Furthermore, considering the occurrence of surface flaws, weldability, and manufacturability, the content is desirably 0.01% or more, and desirably 2.2% or less.
Cuは耐食性向上に有効な元素である。その作用は0.01%から安定して発現する。また、ε-Cu析出による析出強化によって高温強度を向上させるが、過度な添加は熱間加工性を低下させるため上限は3.0%とした。更に、熱疲労特性、製造性および溶接性を考慮すると1.6%以下が望ましい。 Cu is an element effective in improving corrosion resistance. Its action is stably expressed from 0.01%. In addition, high-temperature strength is improved by precipitation strengthening due to precipitation of ε-Cu, but excessive addition lowers hot workability, so the upper limit was made 3.0%. Furthermore, considering thermal fatigue properties, manufacturability and weldability, 1.6% or less is desirable.
Moは、高温における固溶強化に有効な元素であるとともに、耐食性および耐高温塩害性を向上させるため、必要に応じて0.01%以上添加する。3.0%以上の添加で常温延性と耐酸化性が著しく劣化するため、3.0%以下とした。更に、熱疲労特性や製造性を考慮すると、0.3%以上が望ましく、0.9%以下が望ましい。 Mo is an element effective for solid-solution strengthening at high temperatures, and is added in an amount of 0.01% or more as necessary in order to improve corrosion resistance and high-temperature salt damage resistance. Addition of 3.0% or more significantly deteriorates room-temperature ductility and oxidation resistance, so the content was made 3.0% or less. Furthermore, in consideration of thermal fatigue characteristics and manufacturability, it is desirable to be 0.3% or more and 0.9% or less.
WもMo同様、高温における固溶強化に有効な元素であるとともに、Laves相(Fe2W)を生成して析出強化の作用をもたらす。特に、NbやMoと複合添加した場合、Fe2(Nb,Mo,W)のLaves相が析出するが、Wを添加するとこのLaves相の粗大化が抑制されて析出強化能が向上する。これは0.001%以上の添加で作用する。一方、2.0%超の添加ではコスト高になるとともに、常温延性が低下するため、上限を2.0%とした。更に、製造性、低温靭性および耐酸化性を考慮すると、W添加量は1.5%以下が望ましい。Like Mo, W is an element effective for solid-solution strengthening at high temperatures, and produces a Laves phase (Fe 2 W) to bring about precipitation strengthening. In particular, when W is added in combination with Nb or Mo, the Laves phase of Fe 2 (Nb, Mo, W) precipitates, but the addition of W suppresses the coarsening of the Laves phase and improves the precipitation strengthening ability. It works with additions above 0.001%. On the other hand, addition of more than 2.0% increases the cost and reduces room-temperature ductility, so the upper limit was made 2.0%. Furthermore, considering manufacturability, low-temperature toughness and oxidation resistance, the W addition amount is preferably 1.5% or less.
Vは、耐食性を向上させる元素であり、必要に応じて添加される。この効果は0.001%以上の添加で安定して発現する。一方、1%超添加すると析出物が粗大化して高温強度が低下する他、耐酸化性が劣化するため、上限を1%とした。更に、製造コストや製造性を考慮すると、0.08%以上が望ましく、0.5%以下が望ましい。 V is an element that improves corrosion resistance and is added as necessary. This effect is stably exhibited at addition of 0.001% or more. On the other hand, if it is added in excess of 1%, the precipitates become coarse and the high-temperature strength is lowered, and the oxidation resistance is deteriorated, so the upper limit was made 1%. Furthermore, considering the production cost and manufacturability, it is preferably 0.08% or more and 0.5% or less.
Snは、耐食性を向上させる元素であり、中温域の高温強度を向上させるため、必要に応じて添加する。これらの効果は0.01%以上で発現する。一方、0.5%超添加すると製造性および靭性が著しく低下するため、0.5%以下とした。更に、耐酸化性や製造コストを考慮すると、0.1%以上が望ましい。 Sn is an element that improves corrosion resistance, and is added as necessary in order to improve high-temperature strength in the intermediate temperature range. These effects are expressed at 0.01% or more. On the other hand, if added in excess of 0.5%, the manufacturability and toughness are remarkably lowered, so the content was made 0.5% or less. Furthermore, in consideration of oxidation resistance and manufacturing cost, 0.1% or more is desirable.
Niは耐酸性や靭性、高温強度を向上させる元素であり、必要に応じて添加する。これらの効果は0.01%以上で発現する。一方、1.0%超添加するとコスト高になるため、1.0%以下とした。更に、製造性を考慮すると、0.08%以上が望ましく、0.5%以下が望ましい。 Ni is an element that improves acid resistance, toughness, and high-temperature strength, and is added as necessary. These effects are expressed at 0.01% or more. On the other hand, if it is added in excess of 1.0%, the cost increases, so the content was made 1.0% or less. Furthermore, considering manufacturability, 0.08% or more is desirable, and 0.5% or less is desirable.
Mgは、脱酸元素として添加させる場合がある他、スラブの組織を微細化させ、成形性向上に寄与する元素である。また、Mg酸化物はTi(C,N)やNb(C,N)等の炭窒化物の析出サイトになり、これらを微細分散析出させる効果がある。この作用は0.0001%以上で発現し、靭性向上に寄与する。但し、過度な添加は、溶接性、耐食性および表面品質の劣化につながるため、上限を0.01%とした。精錬コストを考慮すると、0.0003%以上が望ましく、0.0010%以下が望ましい。 Mg is sometimes added as a deoxidizing element, and is an element that refines the structure of the slab and contributes to the improvement of formability. Moreover, Mg oxide serves as precipitation sites for carbonitrides such as Ti(C,N) and Nb(C,N), and has the effect of finely dispersing and precipitating them. This action appears at 0.0001% or more and contributes to the improvement of toughness. However, excessive addition leads to deterioration of weldability, corrosion resistance and surface quality, so the upper limit was made 0.01%. Considering refining cost, 0.0003% or more is desirable, and 0.0010% or less is desirable.
Sbは、耐食性と高温強度の向上に寄与するため、必要に応じて0.005%以上添加する。0.5%超の添加により鋼板製造時のスラブ割れや延性低下が過度に生じる場合があるため上限を0.5%とする。更に、精錬コストや製造性を考慮すると、0.01%以上が望ましく、0.3%以下が望ましい。 Sb contributes to the improvement of corrosion resistance and high-temperature strength, so 0.005% or more is added as necessary. Addition of more than 0.5% may excessively cause slab cracking and ductility deterioration during steel sheet production, so the upper limit is made 0.5%. Furthermore, considering the refining cost and manufacturability, it is desirable to be 0.01% or more and 0.3% or less.
Zrは、TiやNb同様に炭窒化物形成元素であり、耐食性、深絞り性を向上させる元素であり、必要に応じて添加する。これらの効果は0.001%以上で発現する。一方、0.3%超の添加により製造性の劣化が著しいため、0.3%以下とした。更に、コストや表面品位を考慮すると、0.1%以上が望ましく、0.2%以下が望ましい。 Zr is a carbonitride-forming element like Ti and Nb, and is an element that improves corrosion resistance and deep drawability, and is added as necessary. These effects are expressed at 0.001% or more. On the other hand, addition of more than 0.3% significantly deteriorates the manufacturability, so the content was made 0.3% or less. Furthermore, considering cost and surface quality, 0.1% or more is desirable, and 0.2% or less is desirable.
Zr、TaおよびHfは、CやNと結合して靭性の向上に寄与するため必要に応じて0.001%以上添加する。但し、0.3%超の添加によりコスト増になる他、製造性を著しく劣化させるため、上限を0.3%とする。更に、精錬コストや製造性を考慮すると、0.01%以上が望ましく、0.08%以下が望ましい。 Zr, Ta and Hf combine with C and N to contribute to the improvement of toughness, so 0.001% or more is added as necessary. However, addition of more than 0.3% increases the cost and significantly deteriorates manufacturability, so the upper limit is made 0.3%. Furthermore, considering refining cost and manufacturability, 0.01% or more is desirable, and 0.08% or less is desirable.
Coは、高温強度の向上に寄与するため、必要に応じて0.001%以上添加する。0.3%超の添加により靭性劣化につながるため、上限を0.3%とする。更に、精錬コストや製造性を考慮すると、0.01%以上が望ましく、0.1%以下が望ましい。 Co contributes to improvement of high-temperature strength, so 0.001% or more is added as necessary. Addition of more than 0.3% leads to deterioration of toughness, so the upper limit is made 0.3%. Furthermore, in consideration of refining cost and manufacturability, 0.01% or more is desirable, and 0.1% or less is desirable.
Caは、脱硫のために添加される場合があり、この効果は0.0001%以上で発現する。しかしながら、0.01%超の添加により粗大なCaSが生成し、靭性や耐食性を劣化させるため、上限を0.01%とした。更に、精錬コストや製造性を考慮すると、0.0003%以上が望ましく、0.0020%以下が望ましい。 Ca is sometimes added for desulfurization, and this effect is exhibited at 0.0001% or more. However, addition of more than 0.01% generates coarse CaS, degrading toughness and corrosion resistance, so the upper limit was made 0.01%. Furthermore, considering the refining cost and manufacturability, it is desirable to be 0.0003% or more and 0.0020% or less.
REMは、種々の析出物の微細化による靭性向上や耐酸化性の向上の観点から必要に応じて添加される場合があり、この効果は0.001%以上で発現する。しかしながら、0.2%超の添加により鋳造性が著しく悪くなる他、延性の低下をもたらすことから上限を0.2%とした。更に、精錬コストや製造性を考慮すると、0.05%以下が望ましい。REM(希土類元素)は、一般的な定義に従い、スカンジウム(Sc)、イットリウム(Y)の2元素と、ランタン(La)からルテチウム(Lu)までの15元素(ランタノイド)の総称を指す。単独で添加してもよいし、混合物であってもよい。 REM may be added as necessary from the viewpoint of improving toughness and oxidation resistance by refining various precipitates, and this effect is exhibited at 0.001% or more. However, addition of more than 0.2% significantly deteriorates castability and lowers ductility, so the upper limit was made 0.2%. Furthermore, considering refining cost and manufacturability, 0.05% or less is desirable. REM (rare earth element) is a generic term for two elements, scandium (Sc) and yttrium (Y), and fifteen elements (lanthanoids) from lanthanum (La) to lutetium (Lu), according to a general definition. They may be added singly or as a mixture.
Gaは、耐食性向上や水素脆化抑制のため、0.3%以下で添加してもよい。硫化物や水素化物形成の観点から下限は0.0002%とすると好ましい。さらに、製造性やコストの観点ならびに、延性や靭性の観点から0.0020%以下が好ましい。 Ga may be added at 0.3% or less in order to improve corrosion resistance and suppress hydrogen embrittlement. From the viewpoint of formation of sulfides and hydrides, the lower limit is preferably 0.0002%. Furthermore, 0.0020% or less is preferable from the viewpoints of manufacturability and cost as well as ductility and toughness.
その他の成分について本発明では特に規定するものではないが、本発明においては、Bi等を必要に応じて、0.001~0.1%添加してもよい。なお、As、Pb等の一般的な有害な元素や不純物元素はできるだけ低減することが好ましい。 Other components are not particularly defined in the present invention, but in the present invention, Bi or the like may be added in an amount of 0.001 to 0.1%, if necessary. In addition, it is preferable to reduce general harmful elements such as As and Pb and impurity elements as much as possible.
次に製造方法について説明する。
本発明の鋼板の製造方法は、製鋼-熱間圧延-焼鈍-酸洗の各工程よりなる。製鋼においては、前記必須成分および必要に応じて添加される成分を含有する鋼を、転炉溶製し続いて2次精錬を行う方法が好適である。溶製した溶鋼は、公知の鋳造方法(連続鋳造)に従ってスラブとする。スラブは、所定の温度に加熱され、所定の板厚に連続圧延で熱間圧延される。熱間圧延は複数スタンドから成る熱間圧延機で圧延された後に巻き取られる。
熱延工程の後の焼鈍は省略しても良い。Next, a manufacturing method will be described.
The steel sheet manufacturing method of the present invention comprises the steps of steelmaking-hot rolling-annealing-pickling. In steelmaking, a method of smelting steel containing the above-mentioned essential components and optionally added components in a converter and then secondary refining is suitable. The melted molten steel is made into a slab according to a known casting method (continuous casting). The slab is heated to a predetermined temperature and hot-rolled to a predetermined plate thickness by continuous rolling. Hot rolling is performed by a hot rolling mill consisting of multiple stands and then coiled.
Annealing after the hot rolling process may be omitted.
ホットスタンプ中における結晶粒径を100~200μmにするため、好ましくは熱延後の仕上げ温度を900~1100℃にする。仕上げ温度900℃未満であると、鋼板の結晶粒径が十分に成長せず、結果としてホットスタンプ後の結晶粒径が100μm以上に成長しない。一方、仕上げ温度が1100℃超であると、鋼板の結晶粒径が成長しすぎ、ホットスタンプ後の結晶粒径が200μm超となる。さらに好ましくは熱延後の仕上げ温度を950℃超にする。仕上げ温度を950℃超にすることで結晶粒径は130μm以上に成長し、中温域の強度も向上させる効果が発現する。
また巻き取り温度が650℃超であると熱延板靭性が低下するため、巻き取り温度を650℃以下にすると好ましい。In order to obtain a crystal grain size of 100 to 200 μm during hot stamping, the finishing temperature after hot rolling is preferably 900 to 1100°C. If the finishing temperature is less than 900° C., the crystal grain size of the steel sheet does not grow sufficiently, and as a result, the crystal grain size after hot stamping does not grow to 100 μm or more. On the other hand, if the finishing temperature exceeds 1100° C., the crystal grain size of the steel sheet will grow excessively, and the crystal grain size after hot stamping will exceed 200 μm. More preferably, the finishing temperature after hot rolling is over 950°C. By setting the finishing temperature to over 950° C., the crystal grain size grows to 130 μm or more, and the effect of improving the strength in the intermediate temperature range is exhibited.
Further, if the coiling temperature exceeds 650°C, the toughness of the hot-rolled sheet is lowered, so it is preferable to set the coiling temperature to 650°C or lower.
次に成形方法について説明する。本発明の鋼板の成形は、鋼板を所定の温度に加熱し高温においてハット形状に成形後冷却するホットスタンプである。加熱温度は900~1000℃とし、成形後、冷却を行う。析出物を微細かつ多量に析出させるため、890~700℃において1分以上10分以下滞留されるように冷却を行う。滞留時間が1分未満であると析出が十分に生じず、析出強化量が小さくなるため下限を1分とする。本時間が過度に長くなると微細に析出した析出物が成長・粗大化し析出強化量が低下する。また、著しく生産性が落ちるため、上限は10分とする。更に、析出物の安定性を考慮すると、1.5分~5分が望ましい。 Next, the molding method will be explained. Forming of the steel sheet of the present invention is a hot stamping method in which the steel sheet is heated to a predetermined temperature, formed into a hat shape at a high temperature, and then cooled. The heating temperature is 900 to 1000° C., and cooling is performed after molding. In order to precipitate a large amount of fine precipitates, cooling is performed at 890 to 700° C. so that the mixture is retained for 1 minute or more and 10 minutes or less. If the residence time is less than 1 minute, precipitation will not occur sufficiently and the amount of precipitation strengthening will be small, so the lower limit is made 1 minute. If this time is excessively long, finely precipitated precipitates grow and coarsen, and the amount of precipitation strengthening decreases. Moreover, the upper limit is set to 10 minutes because the productivity drops significantly. Furthermore, considering the stability of precipitates, 1.5 to 5 minutes is desirable.
本発明において、「ホットスタンプ加工品を構成する自動車ブレーキディスクローター用フェライト系ステンレス鋼板」とは、ホットスタンプ加工を行った後の鋼板を意味する。即ち、ステンレス鋼板を用いてなる自動車ブレーキディスクローター用ホットスタンプ加工品を意味する。
また、ステンレス鋼板を用いてなる自動車ブレーキディスクローター用ホットスタンプ加工品とは、ステンレス鋼板を用いてホットスタンプ加工を行い、自動車ブレーキディスクローター用ホットスタンプ加工品としたものを意味する。
また、ステンレス鋼板を用いてなる自動車ブレーキディスクローターとは、ステンレス鋼板を用いてホットスタンプ加工を行い、さらに加工して自動車ブレーキディスクローターとしたものを意味する。In the present invention, the "ferritic stainless steel sheet for automobile brake disc rotors constituting a hot-stamped product" means a steel sheet after hot-stamping. That is, it means a hot-stamped product for automobile brake disc rotors using a stainless steel plate.
A hot-stamped product for an automobile brake disc rotor using a stainless steel plate means a hot-stamped product for an automobile brake disc rotor obtained by subjecting a stainless steel plate to hot stamping.
An automobile brake disc rotor made of stainless steel plate means an automobile brake disc rotor obtained by subjecting a stainless steel plate to hot stamping and further processing.
表1、表2に示す成分組成の鋼を溶製してスラブに鋳造し、表3、表4に示す熱延条件でスラブを熱間圧延して6mm厚の熱延コイルとし、酸洗を施した。表1のNo.A1~A34は本発明鋼、表2のNo.B1~B14は比較鋼、No.B15は未熱処理鋼である。本発明から外れる数値に下線を付している。 The steels having the compositions shown in Tables 1 and 2 are melted and cast into slabs, the slabs are hot-rolled under the hot-rolling conditions shown in Tables 3 and 4 to form hot-rolled coils with a thickness of 6 mm, and pickled. provided. No. in Table 1. A1 to A34 are steels of the present invention; B1 to B14 are comparative steels; B15 is an unheat treated steel. Numerical values outside the scope of the present invention are underlined.
このようにして得られた熱延板(B15を除く)を、1000℃まで加熱後に890~700℃において2分滞留し、その後水冷するホットスタンプ模擬熱処理(以下単に「疑似熱処理」という。)を施した。疑似熱処理後の鋼板に割れが生じた場合、表4の「疑似熱処理後品質/備考」欄に「割れ」と記載した。 A hot stamping simulated heat treatment (hereinafter simply referred to as “pseudo heat treatment”) is performed by heating the hot-rolled sheet (excluding B15) thus obtained to 1000° C., holding it at 890 to 700° C. for 2 minutes, and then cooling it with water. provided. When cracks occurred in the steel plate after the simulated heat treatment, "crack" was described in the column of "quality after simulated heat treatment/remarks" in Table 4.
ホットスタンプ模擬熱処理材について、t/4部の結晶粒径を測定した(JIS G 0551に準拠、数値は小数点以下を四捨五入)。撮影倍率は50倍、撮影視野数は5視野とし、5視野の平均結晶粒径を算出した。また、同模擬熱処理材について日本電子製200kV電界放出型透過電子顕微鏡(EM-2100F)を用いて、撮影倍率12500倍の明視野観察にて5視野観察し、析出物評価を行った。析出物粒径は、上記明視野観察像に含まれる析出物の円相当径を測定した。粒径500nm以下の析出物について5視野の平均析出物密度を算出した。 The crystal grain size of t/4 part of the hot stamp simulated heat treated material was measured (according to JIS G 0551, the numerical value is rounded off to the nearest whole number). The photographing magnification was 50 times, the number of photographing fields was 5, and the average grain size of the 5 fields was calculated. In addition, using a 200 kV field emission transmission electron microscope (EM-2100F) manufactured by JEOL Ltd., the simulated heat-treated material was observed in 5 fields of bright field observation at a magnification of 12,500 times to evaluate precipitates. For the grain size of precipitates, the circle-equivalent diameter of the precipitates contained in the bright-field observation image was measured. The average precipitate density in 5 fields of view was calculated for precipitates having a grain size of 500 nm or less.
また、ホットスタンプ模擬熱処理材から圧延方向が引張方向となるように高温引張試験片を採取し、300℃および700℃で引張試験を実施し、0.2%耐力を測定した(JIS G 0567に準拠、数値は小数点以下を四捨五入)。ここで、300℃における0.2%耐力が150MPa以上、700℃における0.2%耐力が80MPa以上であれば、一般的なディスクローターへの適用および薄肉化が可能なため、300℃における0.2%耐力を150MPa以上、700℃における0.2%耐力を80MPa以上有するものを合格とし、表3、表4中でA印を記載した。さらに、300℃における0.2%耐力を170MPa以上、700℃における0.2%耐力を100MPa以上有するものは特に優れるものとしてS印を記載した。上記以外は不合格としてX印を記載した。 In addition, a high-temperature tensile test piece was taken from the hot stamping simulated heat treatment material so that the rolling direction was the tensile direction, and a tensile test was performed at 300 ° C. and 700 ° C. to measure the 0.2% proof stress (JIS G 0567 compliant, numbers are rounded to the nearest whole number). Here, if the 0.2% proof stress at 300 ° C. is 150 MPa or more and the 0.2% proof stress at 700 ° C. is 80 MPa or more, it can be applied to a general disc rotor and thinned. A sample having a 2% yield strength of 150 MPa or more and a 0.2% yield strength of 80 MPa or more at 700° C. was regarded as acceptable, and marked A in Tables 3 and 4. Furthermore, those having a 0.2% yield strength of 170 MPa or more at 300° C. and a 0.2% yield strength of 100 MPa or more at 700° C. are marked as particularly excellent. Other than the above, X mark was described as failure.
また、ホットスタンプ前の熱延板について、高温におけるプレス成形性を評価するため、熱延板から圧延方向が引張方向となるように高温引張試験片を採取し、1000℃で引張試験を実施し、破断伸びを測定した(JIS G 0567に準拠、数値は小数点以下を四捨五入)。ここで、1000℃における破断伸びが50%以上であればハット形状に加工可能なため、1000℃における破断伸びを50%以上有するものを合格とし、表3、表4中でA印を記載した。さらに、1000℃における破断伸びを65%以上有するものは特に優れるものとしてS印を記載した。上記以外は不合格としてX印を記載した。 In addition, in order to evaluate the press formability at high temperature of the hot-rolled sheet before hot stamping, a high-temperature tensile test piece was taken from the hot-rolled sheet so that the rolling direction was the tensile direction, and a tensile test was performed at 1000 ° C. , and breaking elongation were measured (according to JIS G 0567, numerical values are rounded off to the nearest whole number). Here, if the breaking elongation at 1000 ° C. is 50% or more, it can be processed into a hat shape, so those having a breaking elongation at 1000 ° C. of 50% or more are accepted. . Furthermore, those having an elongation at break of 65% or more at 1000°C are marked as particularly excellent. Other than the above, X mark was described as failure.
また熱延板靭性を評価するため熱延板からシャルピー試験片(C方向ノッチ)を作製し常温にてシャルピー衝撃試験を行った。3回の試験の平均衝撃値が10J/cm2以下であったときは、鋼板品質の「備考」欄に「靱性不良」と表示した。In addition, in order to evaluate the toughness of the hot-rolled sheet, a Charpy test piece (C-direction notch) was produced from the hot-rolled sheet and subjected to a Charpy impact test at room temperature. When the average impact value of the three tests was 10 J/cm 2 or less, it was displayed as "poor toughness" in the "remarks" column of the steel plate quality.
表1~表4から明らかなように、ホットスタンプ模擬熱処理後の700℃における0.2%耐力は、本発明例が比較例に比べて優れている。また、熱延板の仕上げ温度を950℃超である本発明例は、結晶粒径が130μm以上であり、300℃耐力はすべて「S」であって特に優れることが分かる。上記疑似熱処理後の300℃および700℃における0.2%耐力、熱延板の1000℃における破断伸びのいずれか一方でも不合格である場合、及び熱延板靱性が不良の場合は、ディスクローターとしての適用が不適と判断した。これより、本発明で規定される鋼は、耐熱性と成形性に優れていることがわかる。 As is clear from Tables 1 to 4, the 0.2% proof stress at 700° C. after the simulated hot stamping heat treatment is superior to the comparative examples in the inventive examples. In addition, it can be seen that the invention examples in which the finishing temperature of the hot-rolled sheet is over 950° C. have a crystal grain size of 130 μm or more, and the 300° C. yield strength is all “S”, which is particularly excellent. If either one of the 0.2% yield strength at 300 ° C. and 700 ° C. after the above simulated heat treatment and the breaking elongation at 1000 ° C. of the hot-rolled sheet fails, and if the toughness of the hot-rolled sheet is poor, the disc rotor It was determined that the application as From this, it can be seen that the steel specified in the present invention is excellent in heat resistance and formability.
比較例B1、B2は、それぞれC、N濃度が上限を外れ、鋼板の1000℃破断伸びが不良であった。
比較例B3はSi濃度が下限を外れ、疑似熱処理後の析出物数が不足して300℃および700℃耐力が低かった。比較例B4はSi濃度が上限を外れ、鋼板での1000℃伸びが不良であるとともに、疑似熱処理後の結晶粒径が過小かつ析出物数が過剰であり、割れが生じた。
比較例B5はMn濃度が上限を外れ、300℃および700℃耐力が不足した。
比較例B6、B7は、それぞれP、S濃度が上限を外れ、いずれも鋼板の靱性不良が生じた。
比較例B8はCr濃度が下限を外れ、高温強度が低下して疑似熱処理後の300℃および700℃耐力が不良であった。また、疑似熱処理後の結晶粒径が過大であることから明らかなように鋼板での結晶粒径も過大となり、鋼板の靱性不良が生じた。
比較例B9、B10、B11は、それぞれCr濃度、Ti濃度、Nb濃度が上限を外れ、鋼板での1000℃破断伸びが不良であるとともに、疑似熱処理での析出物数が過剰となり、割れが生じた。In Comparative Examples B1 and B2, the concentrations of C and N deviated from the upper limits, respectively, and the 1000° C. breaking elongation of the steel sheets was poor.
In Comparative Example B3, the Si concentration was below the lower limit, the number of precipitates after the simulated heat treatment was insufficient, and the yield strength at 300°C and 700°C was low. In Comparative Example B4, the Si concentration exceeded the upper limit, the 1000° C. elongation of the steel sheet was poor, the crystal grain size after the simulated heat treatment was too small, the number of precipitates was excessive, and cracks occurred.
In Comparative Example B5, the Mn concentration exceeded the upper limit, and the yield strength at 300°C and 700°C was insufficient.
In Comparative Examples B6 and B7, the concentrations of P and S deviated from the upper limits, respectively, resulting in poor toughness of the steel sheets.
In Comparative Example B8, the Cr concentration was below the lower limit, the high-temperature strength decreased, and the 300° C. and 700° C. yield strengths after the simulated heat treatment were poor. Moreover, as is clear from the fact that the crystal grain size after the simulated heat treatment was excessively large, the crystal grain size in the steel sheet was also excessively large, resulting in poor toughness of the steel sheet.
In Comparative Examples B9, B10, and B11, the Cr concentration, Ti concentration, and Nb concentration deviated from the upper limits, respectively, and the 1000 ° C. breaking elongation of the steel sheet was poor, and the number of precipitates in the pseudo heat treatment became excessive, resulting in cracking. rice field.
比較例B12は熱延の仕上げ温度が上限を外れ、疑似熱処理後の結晶粒径が過大であることから明らかなように鋼板での結晶粒径も過大となり、鋼板の靱性不良が生じた。
比較例B13は熱延の仕上げ温度が下限を外れ、疑似熱処理後の結晶粒径が過小であり、析出物数が過少となった結果、300℃および700℃耐力が不良であった。
比較例B14は熱延の巻取温度が上限を外れ、鋼板の靱性不良となった。In Comparative Example B12, the finishing temperature of hot rolling was above the upper limit, and the grain size of the steel plate after the quasi-heat treatment was too large.
In Comparative Example B13, the finishing temperature of hot rolling was below the lower limit, the crystal grain size after quasi-heat treatment was too small, and the number of precipitates was too small.
In Comparative Example B14, the coiling temperature for hot rolling was above the upper limit, and the toughness of the steel sheet was poor.
B15は、表2の左端に「未」とあり、即ち、ホットスタンプ疑似熱処理を行わずに結晶粒径、析出物数、300℃および700℃耐力の評価を行ったものである。析出が進行せず、析出物数が過少となった結果、300℃および700℃耐力が不良であった。 For B15, the left end of Table 2 indicates "Not", that is, the crystal grain size, the number of precipitates, and the yield strength at 300°C and 700°C were evaluated without hot stamping pseudo heat treatment. Precipitation did not proceed and the number of precipitates was too small, resulting in poor yield strength at 300°C and 700°C.
Claims (9)
C:0.001~0.05%、
N:0.001~0.05%、
Si:0.3~4.0%、
Mn:0.01~2.0%、
P:0.01~0.05%、
S:0.0001~0.02%、
Cr:10~20%、を含有し、さらに
Ti:0.001~0.5%、Nb:0.01~0.8%
を1種または2種含有し、残部がFeおよび不純物であり、
1000℃まで加熱し、その後890~700℃で1分以上10分以下滞留する冷却をする熱処理(以下「ホットスタンプ疑似熱処理」という。)を行ったとき、
結晶粒径が100~200μmとなり、
粒径500nm以下の析出物が0.01~20個/μm2の密度となる、
ホットスタンプ加工用であることを特徴とする自動車ブレーキディスクローター用フェライト系ステンレス鋼板。 in % by mass,
C: 0.001 to 0.05%,
N: 0.001 to 0.05%,
Si: 0.3 to 4.0%,
Mn: 0.01 to 2.0%,
P: 0.01 to 0.05%,
S: 0.0001 to 0.02%,
Cr: 10 to 20%, Ti: 0.001 to 0.5%, Nb: 0.01 to 0.8%
contains one or two types, the balance being Fe and impurities,
When heat treatment (hereinafter referred to as "hot stamp pseudo heat treatment") is performed by heating to 1000 ° C. and then cooling at 890 to 700 ° C. for 1 minute or more and 10 minutes or less,
The crystal grain size is 100 to 200 μm,
Precipitates with a particle size of 500 nm or less have a density of 0.01 to 20 / μm 2 ,
A ferritic stainless steel sheet for automobile brake disc rotors, characterized by being for hot stamping.
C:0.001~0.05%、
N:0.001~0.05%、
Si:0.3~4.0%、
Mn:0.01~2.0%、
P:0.01~0.05%、
S:0.0001~0.02%、
Cr:10~20%、を含有し、さらに
Ti:0.001~0.5%、Nb:0.01~0.8%
を1種または2種含有し、残部がFeおよび不純物であり、
結晶粒径が100~200μmであり、粒径500nm以下の析出物が0.01~20個/μm2の密度で存在する、ホットスタンプ加工品を構成する自動車ブレーキディスクローター用フェライト系ステンレス鋼板。 in % by mass,
C: 0.001 to 0.05%,
N: 0.001 to 0.05%,
Si: 0.3 to 4.0%,
Mn: 0.01 to 2.0%,
P: 0.01 to 0.05%,
S: 0.0001 to 0.02%,
Cr: 10 to 20%, Ti: 0.001 to 0.5%, Nb: 0.01 to 0.8%
contains one or two types, the balance being Fe and impurities,
A ferritic stainless steel sheet for automobile brake disc rotors constituting a hot-stamped product having a grain size of 100 to 200 μm and precipitates having a grain size of 500 nm or less at a density of 0.01 to 20/μm 2 .
B:0.0001~0.0030%、
Al:0.001~4.0%、
Cu:0.01~3.0%、
Mo:0.01~3.0%、
W:0.001~2.0%、
V:0.001~1.0%、
Sn:0.01~0.5%、
Ni:0.01~1.0%、
Mg:0.0001~0.01%、
Sb:0.005~0.5%、
Zr:0.001~0.3%、
Ta:0.001~0.3%、
Hf:0.001~0.3%、
Co:0.001~0.3%、
Ca:0.0001~0.01%、
REM:0.001~0.2%、
Ga:0.0002~0.3%
の1種以上を含有することを特徴とする請求項1~請求項6のいずれか1項に記載の自動車ブレーキディスクローター用フェライト系ステンレス鋼板。 In place of part of the Fe, in mass% further,
B: 0.0001 to 0.0030%,
Al: 0.001 to 4.0%,
Cu: 0.01 to 3.0%,
Mo: 0.01 to 3.0%,
W: 0.001 to 2.0%,
V: 0.001 to 1.0%,
Sn: 0.01 to 0.5%,
Ni: 0.01 to 1.0%,
Mg: 0.0001-0.01%,
Sb: 0.005 to 0.5%,
Zr: 0.001 to 0.3%,
Ta: 0.001 to 0.3%,
Hf: 0.001 to 0.3%,
Co: 0.001 to 0.3%,
Ca: 0.0001 to 0.01%,
REM: 0.001 to 0.2%,
Ga: 0.0002-0.3%
The ferritic stainless steel sheet for automobile brake disc rotors according to any one of claims 1 to 6, characterized in that it contains one or more of:
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| CN116103572B (en) * | 2023-04-11 | 2023-07-07 | 山西建龙实业有限公司 | Steel for bimetallic brake drum and method for preparing hot-rolled steel strip |
Citations (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2004346425A (en) | 2003-04-28 | 2004-12-09 | Jfe Steel Kk | Martensitic stainless steel for disc brakes |
| JP2005126735A (en) | 2003-10-21 | 2005-05-19 | Jfe Steel Kk | Brake disc excellent in tempering softening resistance and manufacturing method thereof |
| JP2005146298A (en) | 2003-11-11 | 2005-06-09 | Jfe Steel Kk | Stainless steel plate for disc brakes with excellent temper softening resistance |
| JP2005307346A (en) | 2004-03-22 | 2005-11-04 | Jfe Steel Kk | Stainless steel plate for disc brakes with excellent heat resistance and corrosion resistance |
| JP2006169582A (en) | 2004-12-15 | 2006-06-29 | Jfe Steel Kk | Stainless steel plate for disc brakes with excellent heat stress cracking resistance |
| JP2006291240A (en) | 2005-04-06 | 2006-10-26 | Jfe Steel Kk | Brake disc with excellent temper softening resistance and toughness |
| JP2006322071A (en) | 2005-04-21 | 2006-11-30 | Jfe Steel Kk | Brake disk having high temper softening resistance |
| WO2008044299A1 (en) | 2006-10-05 | 2008-04-17 | Jfe Steel Corporation | Brake discs excellent in resistance to temper softening and toughness |
| JP2011225948A (en) | 2010-04-21 | 2011-11-10 | Jfe Steel Corp | Cr-containing hot rolled steel sheet for brake disk, and the brake disk |
| WO2014148015A1 (en) | 2013-03-19 | 2014-09-25 | Jfeスチール株式会社 | Stainless steel sheet |
| CN104294160A (en) | 2014-09-09 | 2015-01-21 | 宝钢不锈钢有限公司 | High-hardness high-toughness low-carbon martensite stainless steel and manufacturing method thereof |
| JP2016117925A (en) | 2014-12-19 | 2016-06-30 | 日新製鋼株式会社 | Four wheel stainless steel disk brake rotor and method for manufacturing the same |
| JP2017172038A (en) | 2016-03-17 | 2017-09-28 | 新日鐵住金ステンレス株式会社 | Martensitic stainless steel for brake disc and brake disc |
| JP2019173086A (en) | 2018-03-28 | 2019-10-10 | 日鉄ステンレス株式会社 | Disc brake rotor for automobile |
Family Cites Families (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS51134756A (en) | 1975-05-16 | 1976-11-22 | Furukawa Electric Co Ltd | Method of producing improved polyoxadiazole resin film |
| JPS639819Y2 (en) | 1980-02-01 | 1988-03-23 | ||
| JP3411767B2 (en) * | 1996-01-30 | 2003-06-03 | Jfeスチール株式会社 | High-strength, high-ductility ferrite single-phase Cr-containing steel sheet and method for producing the same |
| US6568512B1 (en) * | 2002-05-16 | 2003-05-27 | International Truck Intellectual Property Company, Llc | Corrosion resistant cast-in insert exciter ring |
| CN100535168C (en) * | 2007-02-16 | 2009-09-02 | 宝山钢铁股份有限公司 | Method for producing hot-rolled ferritic stainless steel strip steel |
| JP5737952B2 (en) * | 2011-01-05 | 2015-06-17 | 日新製鋼株式会社 | Nb-containing ferritic stainless steel hot rolled coil and manufacturing method |
| JP6166540B2 (en) * | 2013-01-28 | 2017-07-19 | 新日鐵住金ステンレス株式会社 | Ferritic stainless steel sheet and ferritic stainless steel molded part manufacturing method for automobile exhaust system members suitable for high temperature press forming |
| WO2014157576A1 (en) * | 2013-03-27 | 2014-10-02 | 新日鐵住金ステンレス株式会社 | Hot-rolled ferritic stainless-steel plate, process for producing same, and steel strip |
| JP5908936B2 (en) * | 2014-03-26 | 2016-04-26 | 新日鐵住金ステンレス株式会社 | Ferritic stainless steel sheet for flange, manufacturing method thereof and flange part |
| JP6550325B2 (en) * | 2015-11-27 | 2019-07-24 | 日鉄ステンレス株式会社 | Ferritic stainless steel hot rolled steel sheet for flange and method of manufacturing the same |
| KR20170075857A (en) * | 2015-12-23 | 2017-07-04 | 주식회사 포스코 | Low hardness martensitic stainless steel and method for manufacturing the same |
| EP3486347B1 (en) * | 2016-10-17 | 2020-10-21 | JFE Steel Corporation | Hot-rolled and annealed ferritic stainless steel sheet and method for producing same |
| MX2019008874A (en) * | 2017-01-26 | 2019-09-18 | Jfe Steel Corp | HOT ROLLED FERRITIC STAINLESS STEEL SHEET AND METHOD FOR THE MANUFACTURE OF THE SAME. |
| JP6537659B1 (en) * | 2018-03-28 | 2019-07-03 | 日鉄ステンレス株式会社 | Martensitic stainless hot rolled steel sheet, method of manufacturing disc brake rotor using the same |
| JP6615256B2 (en) * | 2018-03-30 | 2019-12-04 | 日鉄ステンレス株式会社 | Stainless steel plate and brake system parts |
-
2020
- 2020-03-12 EP EP20778917.3A patent/EP3950969A4/en active Pending
- 2020-03-12 CA CA3133206A patent/CA3133206C/en active Active
- 2020-03-12 JP JP2021509036A patent/JP7179966B2/en active Active
- 2020-03-12 WO PCT/JP2020/010947 patent/WO2020195915A1/en not_active Ceased
- 2020-03-12 KR KR1020217029951A patent/KR102569352B1/en active Active
- 2020-03-12 CN CN202080025398.8A patent/CN113661261B/en active Active
- 2020-03-12 US US17/598,613 patent/US20220177993A1/en active Pending
- 2020-03-12 MX MX2021011538A patent/MX2021011538A/en unknown
Patent Citations (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2004346425A (en) | 2003-04-28 | 2004-12-09 | Jfe Steel Kk | Martensitic stainless steel for disc brakes |
| JP2005126735A (en) | 2003-10-21 | 2005-05-19 | Jfe Steel Kk | Brake disc excellent in tempering softening resistance and manufacturing method thereof |
| JP2005146298A (en) | 2003-11-11 | 2005-06-09 | Jfe Steel Kk | Stainless steel plate for disc brakes with excellent temper softening resistance |
| JP2005307346A (en) | 2004-03-22 | 2005-11-04 | Jfe Steel Kk | Stainless steel plate for disc brakes with excellent heat resistance and corrosion resistance |
| JP2006169582A (en) | 2004-12-15 | 2006-06-29 | Jfe Steel Kk | Stainless steel plate for disc brakes with excellent heat stress cracking resistance |
| JP2006291240A (en) | 2005-04-06 | 2006-10-26 | Jfe Steel Kk | Brake disc with excellent temper softening resistance and toughness |
| JP2006322071A (en) | 2005-04-21 | 2006-11-30 | Jfe Steel Kk | Brake disk having high temper softening resistance |
| WO2008044299A1 (en) | 2006-10-05 | 2008-04-17 | Jfe Steel Corporation | Brake discs excellent in resistance to temper softening and toughness |
| JP2011225948A (en) | 2010-04-21 | 2011-11-10 | Jfe Steel Corp | Cr-containing hot rolled steel sheet for brake disk, and the brake disk |
| WO2014148015A1 (en) | 2013-03-19 | 2014-09-25 | Jfeスチール株式会社 | Stainless steel sheet |
| CN104294160A (en) | 2014-09-09 | 2015-01-21 | 宝钢不锈钢有限公司 | High-hardness high-toughness low-carbon martensite stainless steel and manufacturing method thereof |
| JP2016117925A (en) | 2014-12-19 | 2016-06-30 | 日新製鋼株式会社 | Four wheel stainless steel disk brake rotor and method for manufacturing the same |
| JP2017172038A (en) | 2016-03-17 | 2017-09-28 | 新日鐵住金ステンレス株式会社 | Martensitic stainless steel for brake disc and brake disc |
| JP2019173086A (en) | 2018-03-28 | 2019-10-10 | 日鉄ステンレス株式会社 | Disc brake rotor for automobile |
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| EP3950969A1 (en) | 2022-02-09 |
| CA3133206C (en) | 2023-01-24 |
| US20220177993A1 (en) | 2022-06-09 |
| CN113661261B (en) | 2023-09-19 |
| KR20210129140A (en) | 2021-10-27 |
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