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JPS607004B2 - Directly patented wire manufacturing method - Google Patents
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JPS607004B2 - Directly patented wire manufacturing method - Google Patents

Directly patented wire manufacturing method

Info

Publication number
JPS607004B2
JPS607004B2 JP2171079A JP2171079A JPS607004B2 JP S607004 B2 JPS607004 B2 JP S607004B2 JP 2171079 A JP2171079 A JP 2171079A JP 2171079 A JP2171079 A JP 2171079A JP S607004 B2 JPS607004 B2 JP S607004B2
Authority
JP
Japan
Prior art keywords
temperature
rolling
wire
ductility
billet
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
JP2171079A
Other languages
Japanese (ja)
Other versions
JPS55113839A (en
Inventor
凱朗 山田
忠正 横山
章二 秋田
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Kobe Steel Ltd
Original Assignee
Kobe Steel Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Kobe Steel Ltd filed Critical Kobe Steel Ltd
Priority to JP2171079A priority Critical patent/JPS607004B2/en
Publication of JPS55113839A publication Critical patent/JPS55113839A/en
Publication of JPS607004B2 publication Critical patent/JPS607004B2/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C21METALLURGY OF IRON
    • C21DMODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
    • C21D9/00Heat treatment, e.g. annealing, hardening, quenching or tempering, adapted for particular articles; Furnaces therefor
    • C21D9/52Heat treatment, e.g. annealing, hardening, quenching or tempering, adapted for particular articles; Furnaces therefor for wires; for strips ; for rods of unlimited length
    • C21D9/525Heat treatment, e.g. annealing, hardening, quenching or tempering, adapted for particular articles; Furnaces therefor for wires; for strips ; for rods of unlimited length for wire, for rods

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Physics & Mathematics (AREA)
  • Thermal Sciences (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • Mechanical Engineering (AREA)
  • Materials Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
  • Heat Treatment Of Steel (AREA)
  • Heat Treatment Of Strip Materials And Filament Materials (AREA)

Description

【発明の詳細な説明】 本発明‘ま・直彦パテンテイング線材の製造法1こ関し
、特に鋼材の化学成分組成および熱延条件を特定するこ
とにより、均一微細パーラィト組織を有する伸線加工性
にすぐれた直接パテンティング高炭素鋼線材を得ること
を可能にしたものである。
DETAILED DESCRIPTION OF THE INVENTION Regarding the manufacturing method 1 of the Naohiko patented wire rod of the present invention, in particular, by specifying the chemical composition and hot rolling conditions of the steel material, the wire rod has excellent wire drawability with a uniform fine pearlite structure. This made it possible to obtain directly patented high carbon steel wire rods.

冷間引抜きして使用される高炭素鋼線は、従来熱間圧延
材を、常温まで冷却したのち再加熱して鉛パテンテイン
グまたは空気パテンティングを施す「再熱処理」を経て
、冷間伸線加工々程に付されていたが、近年省エネルギ
やコスト低減の要請、更に公害問題(特に、鉛パテンテ
ィング処理後の線材付着鉛の除去に伴なう有害廃棄物の
発生)等の観点から、熱延材の保有する熱の有効利用と
、鉛パテンティング処理の省略等を狙った「直接パテン
ティング線材」が開発され、いまや鋼線材の主流を占め
るに到っている。
High carbon steel wire used by cold drawing is conventionally hot rolled material, which is cooled to room temperature, then reheated and subjected to lead patenting or air patenting, followed by cold drawing processing. However, in recent years, due to the demand for energy conservation and cost reduction, as well as pollution problems (particularly the generation of hazardous waste due to the removal of lead attached to wires after lead patenting treatment), "Directly patented wire rods" have been developed with the aim of effectively utilizing the heat contained in hot-rolled materials and omitting the lead patenting process, and have now become the mainstream of steel wire rods.

この直接パテンティング線材は、熱延終了後の線材を、
適当な冷却媒体にて調整冷却することにより、そのま・
袷間伸線加工に耐え得る加工性を備えしめたものである
。なお、ここにパテンテイング処理とは、一般にオース
テナィト化温度城にある鋼線を、適当な冷媒にて連続冷
却変態的もしくは恒温変態的に均一な微細パーラィト組
織の鋼となす熱処理をいう。この圧延熱利用の直接パテ
ンティング線材の開発によって、熱延後の2次加工々程
で必要とされていた複数回のパテンティング処理のうち
、第1回目の処理を省略することが可能となったが、更
には再加熱パテンティング工程の全面的徹廃を狙って、
直接熱処理線村を目的の最終線径にまで伸線して、いっ
きに製品とする「直接製品引き」も実用化されつつある
。ところで、上記技術と併行して伸線加工技術自体にも
不断の進歩がみられ、伸線加工能率の一そうの改善をめ
ざして、伸線速度の高速化、あるいは、1パス当りの減
面率を大きくし出来るだけ少ないパス回数で所定減面率
まで伸線しようとする試みが鋭意なされている。
This direct patented wire rod is a wire rod after hot rolling.
By adjusting cooling with an appropriate cooling medium, it can be used as is.
It has workability that can withstand wire drawing processing. Note that the patenting treatment herein refers to a heat treatment in which a steel wire, which is generally in the austenitizing temperature range, is transformed into a steel having a uniform fine pearlite structure through continuous cooling transformation or isothermal transformation using an appropriate coolant. With the development of this direct patenting wire rod that utilizes rolling heat, it has become possible to omit the first of the multiple patenting treatments that were required in the secondary processing steps after hot rolling. However, with the aim of completely eliminating the reheating patenting process,
``Direct product drawing,'' in which directly heat-treated wire is drawn to the desired final wire diameter and then turned into a product, is also being put into practical use. By the way, in parallel with the above-mentioned technology, constant progress is being made in the wire drawing technology itself, with the aim of further improving the wire drawing efficiency, such as increasing the drawing speed or reducing the area per pass. Efforts are being made to increase the wire drawing ratio and reach a predetermined area reduction ratio with as few passes as possible.

この場合、線村の延性が不足すると、伸線加工中に断線
トラブルを生ずるので、これに対処するには延性のすぐ
れた線材を安定して製造供給できること、就中直接パテ
ンティング処理にて製造し得ることが望まれる。しかし
、前記直接パテンティング材の開発は、主に強度レベル
・強度バラツキの改善に主眼をおいて鉛パテンテイング
の再熱処理材並みのものを得ることが目標とされ、1パ
ス当りの減面率の向上・伸線高速化に応え得るものでは
なかった。本発明者等は、上記問題点を解決するために
、窒化物形成元素を徴量添加した高炭素鋼線材を対象と
し、その延性を支配すると考えられる冶金学的諸因子の
挙動について、単に圧延終了時の調整冷却段階のみなら
ず、成分設計、圧延過程およびビレット加熱段階を含め
た直接パテンテイング材製造過程の各段階におけるオー
ステブィト粒度(y粒度)及び窒化物析出挙動等を詳細
に検討した結果、窒化物形成元素としてNを徴量添加し
た糠材においては、ビレット加熱の設定温度がL直接パ
テンティング線材の延性向上の重要な因子であって、そ
の加熱温度を通常採用される範囲(約110000以上
)よりも低温域に設定することが極めて有効であること
を見出した。本発明は上記知見に基づいて完成されたも
のである。.すなわち、本発明は、C、Si、Mnおよ
び必要に応じてCrをそれぞれ一定量含み、かつ窒化物
形成元素としてAIを約0.02〜0.1%含有する高
炭素鋼ビレットを約800〜1050q○の温度に加熱
したのち、熱間圧延を行なうことにより、窒化アルミニ
ウム(AIN)約3伽皿以上析出した鋼線材を得「なお
最終熱間仕上圧延ののち巻取り1こ到るまでの間に、該
鋼線材を調整冷却して均一微細パーライト組織を与える
ようにした直接パテンティング線材の製造法を提供する
ものであり、これにより、再加熱処理を施すことなく、
冷間伸線加工を行なうことを可能とし、かつ冷間伸線に
おける高速伸線加工、1パス当りの滅面率の増大に耐え
得る十分な延性を保証したものである。
In this case, if the ductility of the wire strip is insufficient, wire breakage will occur during the wire drawing process, so in order to deal with this problem, it is necessary to stably manufacture and supply wire rods with excellent ductility. It is hoped that this will be possible. However, the development of the directly patented material was aimed at improving the strength level and strength variation, and aimed at obtaining a material comparable to reheated lead patented material, with the aim of reducing the area reduction rate per pass. It was not possible to meet the demands for improvement and faster wire drawing. In order to solve the above problems, the present inventors focused on high carbon steel wire rods containing nitride-forming elements, and investigated the behavior of metallurgical factors that are thought to control the ductility of the wire rods by simply rolling. As a result of a detailed study of the austevite grain size (y grain size) and nitride precipitation behavior, etc. at each stage of the direct patenting material manufacturing process, including not only the adjustment cooling stage at the end, but also the component design, rolling process, and billet heating stage, we found that: In bran material to which N is added as a nitride-forming element, the set temperature for billet heating is an important factor in improving the ductility of L directly patented wire rods, and the heating temperature is within the range usually adopted (approximately 110,000 We have found that it is extremely effective to set the temperature at a lower temperature than the above). The present invention was completed based on the above findings. .. That is, the present invention provides a high carbon steel billet containing C, Si, Mn and, if necessary, Cr in certain amounts, and about 0.02 to 0.1% of AI as a nitride-forming element. After heating to a temperature of 1050q○, hot rolling was performed to obtain a steel wire rod in which approximately three or more plates of aluminum nitride (AIN) were precipitated. In the meantime, the present invention provides a method for directly producing a patented wire rod in which the steel wire rod is controlled and cooled to give a uniform fine pearlite structure.
This makes it possible to perform cold wire drawing, and ensures sufficient ductility to withstand high-speed wire drawing in cold wire drawing and an increase in surface loss per pass.

なお、従来にも、微細パーラィト鋼の延性改善策として
、窒化物形成元素(AI、Ti、Nb等)を徴量添加す
るとともに、ビレツト圧延温度を規定することにより、
鋼中窒素を窒化物として固定し「かつその窒化物をオー
ステナィト粒の微細化にも役立たせるようにした鋼線の
製造法が提案されているが(特開昭49一123923
号、特公昭47一51684号等)、これらはいずれも
再加熱パテンティング材を対象としたものであって、本
発明のように直接パテンティング材の延性改善を企図し
たものではない。
In addition, conventional measures to improve the ductility of fine pearlitic steel include adding nitride-forming elements (AI, Ti, Nb, etc.) and regulating the billet rolling temperature.
A method for manufacturing steel wire has been proposed in which nitrogen in steel is fixed as nitride and the nitride is also used to refine the austenite grains (Japanese Patent Laid-Open No. 49-123923).
(Japanese Patent Publication No. 47-51684, etc.), these are all aimed at reheated patented materials, and are not intended to directly improve the ductility of patented materials as in the present invention.

また、従来法では、ビレット加熱時の未溶解窒化物量を
減少させ、あるいはその完全固熔を狙うのが一般であり
、かつそのために加熱温度を約1100q0以上の高温
に設定していた。
Furthermore, in conventional methods, the aim is generally to reduce the amount of undissolved nitrides during billet heating, or to completely solidify them, and for this purpose, the heating temperature is set at a high temperature of about 1100 q0 or more.

しかし、本発明者等の詳細な観察によれば、直接パテン
ティング材の製造過程における窒化物の析出挙動に関し
、一旦オーステナィト地に園溶した窒化物は、圧延過程
及びその後巻取りに到る調整冷却過程において殆んど再
析出しないことが明らかにされている。かかる事実をも
とに従釆法をふりかえってみると、圧延後約950qo
前後に再加熱パテンティングを施していた従来法では、
再加熱時に多量の窒化物が析出するため、従来法のビレ
ット加熱温度条件では、直接パテンティング材の延性改
善には窒化物形成元素の十分な添加効果を期待すること
はできなかったことが分る。すなわち、従来法の加熱条
件では、AI、V等の窒化物は殆んど残留せず、直接パ
テンティング材の延性改善に対し、これら添加元素の効
果は何ら生かされていないのである。このように、本発
明方法における高炭素鋼線材の延性改善のメカニズムは
前記従来法と本質的に異なるものと言うことができる。
本発明に用いられる鋼は次の如き成分元素を含有する。
Cは、鋼線の高強度化のため約0.6%以上を必要とす
る。
However, according to detailed observations by the present inventors, with regard to the precipitation behavior of nitrides during the manufacturing process of direct patenting materials, nitrides once dissolved in the austenitic material are difficult to control during the rolling process and subsequent winding process. It has been shown that almost no redeposition occurs during the cooling process. When we look back at the Jikou method based on these facts, we find that approximately 950 qo after rolling.
In the conventional method, which applied reheating patenting before and after,
Because a large amount of nitride precipitates during reheating, it was found that under the billet heating temperature conditions of the conventional method, it was not possible to expect a sufficient addition effect of nitride-forming elements to improve the ductility of directly patented materials. Ru. That is, under the heating conditions of the conventional method, almost no nitrides such as AI and V remain, and the effects of these additive elements are not utilized in any way to improve the ductility of the direct patenting material. As described above, it can be said that the mechanism of improving the ductility of high carbon steel wire in the method of the present invention is essentially different from that in the conventional method.
The steel used in the present invention contains the following constituent elements.
C is required to be about 0.6% or more in order to increase the strength of the steel wire.

但し、多?ぎると健性‘こ有害な初析セメンタィトがy
粒界に析出するので、約1.0%を上限とするのが望ま
しい。Siは、鋼線の強度向上に有用であるが、過度に
加えると、フェライト自体の延性低下を招くので、約2
.0%以下の範囲で加えられる。
However, many? Too much pro-eutectoid cementite is harmful to health.
Since it precipitates at grain boundaries, it is desirable that the upper limit be about 1.0%. Si is useful for improving the strength of steel wires, but if added in excess, it will reduce the ductility of the ferrite itself, so approximately 2
.. It is added in a range of 0% or less.

Mnは、鋼の焼入性改善に効果を有するほか、パーラィ
トラメラー間隔の繊密化による高強度化を図るのに必須
の成分元素であり、このために約0.3%以上添加され
る。
Mn is effective in improving the hardenability of steel, and is also an essential component element for increasing strength by making the pearlite lamellar spacing more dense, and for this purpose it is added in an amount of about 0.3% or more. .

特に、大経線材の高強度化には、添加量を増すことが望
ましい。しかし、多すぎると、パーラィト変態の著しい
遅滞を招き、圧延・パテンティング工程の時間内で変態
を完了させることができず、延性に最も有害な過冷組織
(マルテンサィト)が綱紀織内に部分的に出現する弊害
を伴なうので、約1.4%を上限とすることが望ましい
。AIは、オーステナィト粒(ッ粒度)の微細化と鋼中
Nの固定のために加えられる。
In particular, it is desirable to increase the amount added to increase the strength of large meridian wire rods. However, if the amount is too large, it will cause a significant delay in pearlite transformation, making it impossible to complete the transformation within the time required for rolling and patenting processes. Therefore, it is desirable to set the upper limit to about 1.4%. AI is added to refine the austenite grains (grain size) and fix N in the steel.

y粒を微細化するには、後述のように、ビレット加熱時
に約3伽皿以上析出させておくことが必要であり、特に
約5の側以上が好ましい。このため、約0.02%以上
のAIの添加が必要である。窒素固定の観点からは「A
I添加量が多い程有利であるが、多すぎると、オーステ
ナィト粒界上に過度にAINが析出するほか、AI20
3の生成量も増加し、延性を害することとなるので、好
ましくは上限を約0.1%とする。Nは、上記山と結合
し、AINを形成するための必須元素であるが、その量
は、高炭素鋼線材に通常含まれる量(数十柳程度)で十
分である。
In order to refine the Y grains, as will be described later, it is necessary to precipitate approximately 3 or more grains during billet heating, and it is particularly preferable to precipitate approximately 5 grains or more. For this reason, it is necessary to add approximately 0.02% or more of AI. From the perspective of nitrogen fixation, “A
The larger the amount of I added, the more advantageous it is, but if it is too large, AIN will precipitate excessively on the austenite grain boundaries, and AI20
Since the amount of 3 produced also increases and impairs ductility, the upper limit is preferably set to about 0.1%. N is an essential element for combining with the above-mentioned peaks to form AIN, but the amount normally contained in high carbon steel wire rods (about several tens of willows) is sufficient.

但し、必要に応じ、約10■肌程度まで添加することを
妨げない。上記諸元素のほか、次の元素を加えることが
できる。
However, this does not prevent it from being added up to about 10 cm if necessary. In addition to the above elements, the following elements can be added.

Crは、前記Mnと同様、焼入性の改善、パーラィトラ
メラー間隔の繊密化による強度改善の効果を有する。
Like Mn, Cr has the effect of improving hardenability and improving strength by making the spacing between pearlite lamellas finer.

但し、過度の添加はMnと同じく、パーラィト変態の遅
滞化を招くので、約1.5%以下の範囲で加えられる。
その他、PおよびS等の不純物は、この種の鋼に通常許
容される範囲内で存在して構わない。
However, like Mn, excessive addition causes retardation of pearlite transformation, so it should be added in an amount of about 1.5% or less.
Other impurities such as P and S may be present within the range normally allowed for this type of steel.

次に、ビレットの加熱、圧延条件等について説明する。
高炭素鋼線材の圧延におけるビレツト加熱温度は、従来
一般に約1100qo以上とされているが、本発明にお
いては、約800〜1050qoに設定される。
Next, billet heating, rolling conditions, etc. will be explained.
The billet heating temperature during rolling of high carbon steel wire rods has conventionally been generally set at about 1100 qo or higher, but in the present invention it is set at about 800 to 1050 qo.

ビレットを約105000以下の低温度に加熱すること
により、延性に有害な窒素を未溶解の窒化物として固定
することができ、またこの禾溶解窒化物は、最終圧延後
、パーラィト変態が開始するまでの間に生じるy粒の成
長を阻止し、組織の微細化に役立たせることができる。
かかる窒素固定のためには、圧延作業の障害を生じない
範囲内で、できるだけ加熱温度を低くすることが望まし
く、本発明においては、約800午○以上に設定される
。800℃未満では、NはMNとして固定されるものの
、圧延中の変形抵抗が大きくなり、機械への圧延負荷が
増し、線村表面癖が発生する。
By heating the billet to a low temperature of about 105,000 °C or less, nitrogen, which is harmful to ductility, can be fixed as undissolved nitrides, and the dissolved nitrides remain after the final rolling until pearlite transformation begins. This can prevent the growth of y-grains that occur during the process, and can help refine the structure.
For such nitrogen fixation, it is desirable to keep the heating temperature as low as possible within a range that does not interfere with the rolling operation, and in the present invention, it is set to about 800 pm or higher. At temperatures below 800°C, although N is fixed as MN, the deformation resistance during rolling increases, the rolling load on the machine increases, and surface roughness occurs.

y粒の成長を阻止するには、ビレットの加熱時にNNを
約3■風以上残留させておくことが有効である。
In order to prevent the growth of Y-grains, it is effective to leave approximately 3 mm or more of NN remaining when heating the billet.

特に、約5の皿以上が望ましい。このためには、ビレッ
ト加熱温度は約1000q○以下とすることが望ましい
。上述のごときビレット加熱温度の調節によるビレット
加熱時のy粒の大きさは、最終圧延後のy粒径に強い影
響を与え、従来法より低温度で行なうことにより、一そ
う微細な結晶粒を得ることができる。
In particular, about 5 plates or more are desirable. For this purpose, it is desirable that the billet heating temperature be about 1000q○ or less. The size of the y grains during billet heating by adjusting the billet heating temperature as described above has a strong influence on the y grain size after final rolling. Obtainable.

これにより、従来の直接パテンティング材に比し、すぐ
れた延性が保証される。ビレットは、上記加熱ののち、
熱間圧延に付される。
This ensures superior ductility compared to conventional directly patented materials. After the billet is heated as described above,
Subjected to hot rolling.

熱間圧延では、前記ビレット加熱時に残留せしめた山N
が圧延中の昇温等により固溶・消失するのを防ぐため、
鋼線温度はビレット加熱温度(約1050午0)を越え
ないよう、温度調整を行なうことが望ましいづなお、y
粒の微細化・パーラィト組織の微細化をより効果的にし
、得られる鋼線材の延性を一そう高めるために、例えば
中間スタンドから仕上スタンドまで、または仕上スタン
ドでの圧延を温度約90000以下で行なう、所謂「低
温圧延」を採用することも有効である。
In hot rolling, the mountains N remaining during billet heating are removed.
In order to prevent solid solution and disappearance due to temperature rise during rolling,
It is desirable to adjust the steel wire temperature so that it does not exceed the billet heating temperature (approximately 1050:00).
In order to make the grain refinement and pearlite structure more effective and further increase the ductility of the obtained steel wire, rolling from the intermediate stand to the finishing stand or at the finishing stand is performed at a temperature of about 90,000 or less. It is also effective to employ so-called "low temperature rolling".

また、仕上圧延機列に付帯する水冷帯を出た直後(水冷
帯出口または水袷帯冷却直後)の線材温度、すなわち、
圧延仕上温度が高くなるとッ粒は粗くなり延性が低下す
る。
In addition, the wire temperature immediately after exiting the water cooling zone attached to the finishing mill row (immediately after the water cooling zone exit or water cooling zone cooling), that is,
As the rolling finishing temperature increases, the grains become coarser and the ductility decreases.

しかし、遊離のN(MNになっていないN)量は、加熱
温度に依存し、圧延終了温度(水袷帯出口温度)にはほ
とんど依存しないため低温加熱の場合、仕上温度は通常
の800〜950℃でよい。仕上温度をあまり低温に設
定すると内外部の組織差を生じ好ましくない。一方、高
温に設定しすぎた場合は、スケールが多くなり歩留りの
低下、あるいはy粒粗大化による機械的性質低下が生ず
る。圧延後の鋼線材の冷却方法に特別の制限はないが、
微細パーラィト組織が与えられるごとき適当な調整冷却
を行なうべきことは言うまでもない。
However, the amount of free N (N that has not become MN) depends on the heating temperature and is almost independent of the rolling end temperature (water belt outlet temperature). 950°C is sufficient. If the finishing temperature is set too low, a difference in structure between the inside and outside will occur, which is undesirable. On the other hand, if the temperature is set too high, scale increases and the yield decreases, or mechanical properties deteriorate due to coarse grains. There are no special restrictions on the method of cooling the steel wire rod after rolling, but
Needless to say, appropriate controlled cooling should be carried out to provide a fine pearlite structure.

第1図は、AI約0.036%を含むSWRS82B相
当材のビレツトを加熱したのち熱間圧延に付し、最終圧
延後、ループ状に巻取った鋼線材について、変態開始ま
での間のy粒度に対するビレット加熱温度の影響を示し
たグラフである。図中、曲線1は、ビレット加熱温度:
1000oo、2は同110000、3は同1200q
oの各場合である。図より、加熱温度が1100午0以
上の場合、粒成長により粗大化するのに対し、本発明方
法により1050qo以下にした場合、巻取り直後のy
粒も微細で、かつ粒成長は殆んど起こらず、好ましい細
粒組織が与えられることがわかる。次に、実施例を挙げ
て本発明方法及び得られる鋼線材特性について具体的に
説明する。
Figure 1 shows the y of a steel wire rod that is heated and hot rolled after heating a billet of a material equivalent to SWRS82B containing about 0.036% AI, and wound up into a loop after final rolling until the start of transformation. It is a graph showing the influence of billet heating temperature on particle size. In the figure, curve 1 is billet heating temperature:
1000oo, 2 is 110000, 3 is 1200q
In each case o. From the figure, when the heating temperature is 1100 qo or more, the grains become coarse due to grain growth, whereas when the heating temperature is 1050 qo or less by the method of the present invention, the y immediately after winding
It can be seen that the grains are fine and grain growth hardly occurs, giving a preferable fine grain structure. Next, the method of the present invention and the properties of the obtained steel wire will be specifically explained with reference to Examples.

なお、第1表および第3表中、圧延仕上温度とは、仕上
圧延後の水冷帯出口温度である。実施例 1 第1表に示す凶、‘B}2種の鋼を供試材とし、ステル
モァラィン(衝風冷却方式)を用い、直接パテンティン
グ材を製造し、75%伸線加工を行なった。
In addition, in Tables 1 and 3, the finishing rolling temperature is the water cooling zone outlet temperature after finishing rolling. Example 1 Using two types of steel shown in Table 1 as test materials, a patented material was directly produced using Stelmorline (blast cooling method), and 75% wire drawing was performed.

圧延条件および得られた線材の特性を第2表に示す。第
1表 供試材の化学成分組成(wt%)第2表 圧延条
件及び線材の特性 ※1:線材径:7側め、※2:線材径:11伽の。
Table 2 shows the rolling conditions and properties of the obtained wire rod. Table 1: Chemical composition of sample materials (wt%) Table 2: Rolling conditions and wire properties *1: Wire diameter: 7th side, *2: Wire diameter: 11th.

第2表に示されるように、本発明方法による低温ビレツ
ト加熱材(No.2、3、5「 6)は、ロッド(直接
パテンティング材)および伸線後(75%伸線材)のい
ずれにおいても、従来の高温加熱材のそれよりすぐれた
延性を有している。また、試験No.2とNo.3、N
o.5とNo.6のそれぞれの比較から明らかなように
、低温圧延による延性向上効果が得られることも認めら
れる。以上のように、本発明方法によれば、直接パテン
ティング線村の延性を顕著に高め、その伸線加工能率を
大きく改善することができる。
As shown in Table 2, the low-temperature billet heated materials (Nos. 2, 3, 5 and 6) produced by the method of the present invention can be used both in the rod (directly patented material) and after wire drawing (75% wire drawn material). also has better ductility than that of conventional high-temperature heating materials.Also, test No. 2 and No. 3, N
o. 5 and no. As is clear from the comparison of No. 6, it is also recognized that the effect of improving ductility can be obtained by low-temperature rolling. As described above, according to the method of the present invention, the ductility of the directly patented wire village can be significantly increased, and the wire drawing efficiency can be greatly improved.

また、ビレットの加熱温度が低いことは、ビレット加熱
時の脱炭の防止、スケール付着量の減少効果をもたらし
、得られる鋼線材の表面品質の向上にも資するものであ
る。なお、本発明方法は、AI以外の窒化物形成元素(
例えば「Nb、Ti、Zr、V等)をAIと同等程度加
えた鋼を用いた直接パテンテイング線材の製造に適用し
、その延性を高めることも可能であるが、多すぎるとN
と同機過度の窒化物が析出し、延性を損なう。実施例
2 第3表に示すに’、(D}2種のバネ用鋼を供試材とし
、実施例1と同様の方法で直綾パテンティング材を製造
した。
Furthermore, the low heating temperature of the billet has the effect of preventing decarburization and reducing the amount of scale adhesion during billet heating, and also contributes to improving the surface quality of the obtained steel wire rod. Note that the method of the present invention can be applied to nitride-forming elements other than AI (
For example, it is possible to directly manufacture patented wire rods using steel to which Nb, Ti, Zr, V, etc. are added to the same extent as AI, and increase its ductility, but if too much Nb, Ti, Zr, V, etc.
Excessive nitrides precipitate and impair ductility. Example
2 As shown in Table 3, straight twill patenting materials were manufactured in the same manner as in Example 1 using two types of spring steels as test materials.

圧延条件および得られた結果を第4表に示す。第3表
供試材の化学成分組成(wt% 第4表 圧延条件および線材の特性 ※3:線材径:8帆の、 ※4:線材律:9柳の第4表
に示されるように、本発明方法による加熱材(No.9
「 10、12)は、従来の高温加熱材(No.7、8
、11)の場合よりもすぐれた延性を有している。
The rolling conditions and the results obtained are shown in Table 4. Table 3
Chemical composition of the sample material (wt%) Table 4 Rolling conditions and wire rod characteristics *3: Wire diameter: 8 wire, *4: Wire rod rule: 9 Yanagi As shown in Table 4, the method of the present invention heating material (No. 9
"10, 12) are conventional high temperature heating materials (No. 7, 8)
, 11).

従来の高温加熱(1100午C)により鋼C「Dを処理
すると圧延直後、水冷を充分に行なってもベイナイトが
出現する。これに対して、本発明方法の低温加熱によれ
ばVNやAINはもちろん、VC(V4C3)も溶け残
ったまま圧延されるので、C、Nの固定による延性向上
効果だけでなく、固港Vなどの減少による焼入性低下効
果も加わり、圧延材の引張り強さが低下して延性は改善
される。また「NbはVに比べより高温まで炭窒化物が
安定であるため「圧延後のy粒の粗大化を防止し「過冷
組織防止に効果がある。
When steel C and D are treated by conventional high-temperature heating (1100 pm), bainite appears immediately after rolling, even after sufficient water cooling.On the other hand, with the low-temperature heating of the present invention, VN and AIN are Of course, since VC (V4C3) is also rolled while remaining melted, it not only improves ductility by fixing C and N, but also reduces hardenability by reducing hardness V, etc., and the tensile strength of the rolled material increases. The carbonitride of Nb is stable even at higher temperatures than V, so it is effective in preventing the coarsening of grains after rolling and preventing overcooling.

【図面の簡単な説明】[Brief explanation of drawings]

第1図は、線材ループ巻取り後のy粒度変化に対するビ
レット加熱温度の影響を示すグラフである。 第1図
FIG. 1 is a graph showing the influence of billet heating temperature on y particle size change after wire loop winding. Figure 1

Claims (1)

【特許請求の範囲】[Claims] 1 C0.6〜1.0%、Si2.0%以下、Mn0.
3〜1.4%、Al0.02〜0.1%を含む高炭素鋼
のビレツトを、温度800〜1050℃に加熱したのち
、熱間圧延し、最終熱間仕上圧延後から巻取りに至る間
に鋼線材を調整冷却して均一微細パーライト組織となす
ことを特徴とする延性のすぐれた直接パテンテイング線
材の製造法。
1 C0.6-1.0%, Si2.0% or less, Mn0.
A billet of high carbon steel containing 3 to 1.4% Al and 0.02 to 0.1% Al is heated to a temperature of 800 to 1050°C, then hot rolled, and after the final hot finish rolling, it is rolled up. A method for producing a direct patented wire rod with excellent ductility, characterized by controlling and cooling the steel wire rod to form a uniform fine pearlite structure.
JP2171079A 1979-02-23 1979-02-23 Directly patented wire manufacturing method Expired JPS607004B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2171079A JPS607004B2 (en) 1979-02-23 1979-02-23 Directly patented wire manufacturing method

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2171079A JPS607004B2 (en) 1979-02-23 1979-02-23 Directly patented wire manufacturing method

Publications (2)

Publication Number Publication Date
JPS55113839A JPS55113839A (en) 1980-09-02
JPS607004B2 true JPS607004B2 (en) 1985-02-21

Family

ID=12062608

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2171079A Expired JPS607004B2 (en) 1979-02-23 1979-02-23 Directly patented wire manufacturing method

Country Status (1)

Country Link
JP (1) JPS607004B2 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6448603U (en) * 1987-09-21 1989-03-27

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5757837A (en) * 1980-09-24 1982-04-07 Sumitomo Metal Ind Ltd Production of high carbon high tensile wire rod
JPH0717126B2 (en) * 1984-03-01 1995-03-01 株式会社ブリヂストン High durability radial tire
US5658402A (en) * 1993-05-25 1997-08-19 Nippon Steel Corporation High-carbon steel wire rod and wire excellent in drawability and methods of producing the same
WO1999011836A1 (en) 1997-08-28 1999-03-11 Sumitomo Electric Industries, Ltd. Steel wire and method of manufacturing the same
KR20000042052A (en) * 1998-12-24 2000-07-15 이구택 Method for producing high intensity wire rod for concrete steel fiber
KR100797303B1 (en) 2006-09-04 2008-01-24 주식회사 포스코 Manufacturing method of tire cord wire for mechanical peeling with excellent scale adhesion

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6448603U (en) * 1987-09-21 1989-03-27

Also Published As

Publication number Publication date
JPS55113839A (en) 1980-09-02

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