JPS647130B2 - - Google Patents

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Publication number
JPS647130B2
JPS647130B2 JP17418684A JP17418684A JPS647130B2 JP S647130 B2 JPS647130 B2 JP S647130B2 JP 17418684 A JP17418684 A JP 17418684A JP 17418684 A JP17418684 A JP 17418684A JP S647130 B2 JPS647130 B2 JP S647130B2
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JP
Japan
Prior art keywords
rolling
ferrite
steel
temperature
cooling
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
JP17418684A
Other languages
Japanese (ja)
Other versions
JPS6156233A (en
Inventor
Giichi Matsumura
Takehide Senuma
Hiroshi Yada
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.)
Nippon Steel Corp
Original Assignee
Nippon Steel Corp
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 Nippon Steel Corp filed Critical Nippon Steel Corp
Priority to JP17418684A priority Critical patent/JPS6156233A/en
Publication of JPS6156233A publication Critical patent/JPS6156233A/en
Publication of JPS647130B2 publication Critical patent/JPS647130B2/ja
Granted legal-status Critical Current

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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
    • C21D8/00Modifying the physical properties of ferrous metals or ferrous alloys by deformation combined with, or followed by, heat treatment

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  • 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)

Description

【発明の詳細な説明】[Detailed description of the invention]

(産業上の利用分野) 本発明は自動車の強度部材やホイール,溶接鋼
管用素材あるいは構造部材等に用いられる高張力
鋼材の製造方法に関するものである。 (従来の技術) 鋼の種々の強化方法のうちで結晶粒の微細化は
強度と共に靭性をも高くする唯一の方法として知
られており、特に熱延ままで使用される鉄鋼材料
の材質向上を計る際には殆んどの場合に先ず考慮
されねばならない重要な技術である。従来の細粒
化技術で工業的に達成されているのは小さくて4
〜6μ程度である。これは通常制御圧延法と呼ば
れる方法で行われており、Nb等の合金元素を含
む鋼を比較的低温域で強い圧延を行う技術であ
る。この場合Nbが圧延ままで固溶している必要
があるので、圧延前に例えば1200℃以上という高
温で加熱を行なつてNbを固溶させ、しかるのち
に仕上圧延は800℃以下という低温域で行うので、
鋼板の温度低下を待つため生産効率が著しく低下
し、また圧延時の変形抵抗が著しく高くなるた
め、圧延機に対する負荷が大であるなど工業的に
欠点がある。この他に低温域で加熱して圧延を行
う方法、あるいは圧延後強制冷却を行う方法など
種々提案されているが、いずれも上記粒径範囲内
に留つている。 最近特殊元素を含まない炭素鋼により粒径3〜
4μ以下の超微細粒を得る方法(特開昭58―
123823)が示されたが、この方法は圧延時に大き
な圧下率を要し、設備的な制約を受ける。 (発明が解決しようとする問題点) 本発明は粒径3〜4μ以下の超微細フエライト
組織からなる高材質高張力鋼材を通常の熱延設備
により生産性を低下させる事なく安価に製造する
事を目的とする。なお超微細フエライト組織とは
個々の結晶粒径が3〜4μ以下(粒度番号13以上)
のフエライトが体積率で60%以上を占める組織を
意味する。 (問題点を解決するための手段) 本発明の要旨は下記の通りである。すなわち 重量で、 C:0.05〜0.2% Si:0.01〜1.0% Mn:0.3〜2.0% を含み、さらに、 Ti,Nb,Taの1種または2種以上をそれぞれ
0.01〜0.1%含有する鋼を、Ac3点以上1100℃以下
の温度に加熱した後、冷却過程において熱間圧延
を行ない、その際、圧延最終段で15秒間以内に合
計50%以上の圧下を加えるとともに仕上温度を
Ar3点〜Ar3+100℃とし、熱間圧延終了後5秒間
以内に10℃/s以上の冷却速度で冷却することを
特徴とする超細粒低合金熱延高張力鋼の製造方
法。 以下に本発明の内容を詳細に説明する。 本発明の骨子は熱間圧延開始時に鋼中に微細な
析出物を適当量存在させておき、圧延によつてそ
れらの析出物を変態核とするフエライト変態を誘
起させる事である。従来、鋼が高温のオーステナ
イトより冷却によつてフエライト変態する際に析
出物等が存在すると、結晶粒界以外にそれらの析
出物等を変態核になる事は知られていた。一方本
発明者らは以前に炭素鋼がオーステナイトからフ
エライトに変態する直前に大圧下を加えると、フ
エライト変態が誘起され微細なフエライト粒が生
成する事を示したが、この際に微細な析出物が適
当量存在すると、加工誘起変態が容易に起り、1
パスの圧下率が比較的小さくとも超微細フエライ
ト組織が生成する事を見出した。第2図は0.15C
―1.5Mn鋼に種々のNb量を添加したものにつき、
加熱温度と圧延圧下率を変えて圧延した後のフエ
ライト粒度を示すが、これにより低温加熱で圧延
前にNbが析出したものは低圧下率でも組織が微
細化することがわかる。 以下に本発明の構成を説明するが、先ず、鋼成
分について説明する。 Cは炭素鋼の組織,材質を左右する主成分であ
るが、0.05%未満では高強度が得られず、0.2%
を超えると加工による変態が不十分となり、また
溶接性や加工性も低下する。そこで0.05%≦C≦
0.2%に限定した。 Mnは強度―靭性バランスを向上させ組織微細
化にも効果もあるので、添加は望ましいが、その
効果は0.3%未満では現れず、また2%を超える
と変態点が低下しすぎでフエライト変態が不十分
となる。そこで0.3%≦Mn≦2.0%に限定した。 Siは0.01%以上を添加すると鋼板の強度―延性
バランスを向上させるので添加が望ましいが、1
%を超えると溶接性を損なうことがあるので、
0.01%≦Si≦1.0%に限定した。 Ti,NbおよびTaは炭化物(および炭窒化物)
を形成し変態核となるので、本発明では必須の元
素である。これらのうち1種または2種以上の合
計添加量が0.01%未満では析出物の量が少なく効
果が小さい。また0.1%を超えると析出物のサイ
ズが不適当となり効果が減ずる。そこでTi,Nb
およびTaのうち1種または2種以上の合計添加
量を0.01%〜0.1%に限定した。 上記以外の特殊元素(V等)は仕上圧延開始時
に適当量が析出するものは有効であるが、Ti,
Nb,Taほどの効果は示さないので特に限定はし
ない。しかしながら補助的に添加する事は差支え
ない。析出物の形成温度が低く、熱履歴に拘らず
仕上圧延開始時に固溶している様な元素(Mo
等)は効果がない。 次に、本発明の製造方法について説明する。本
発明では圧延素材であるスラブの加熱温度は低温
である必要がある。従来の制御圧延においては、
Nb等の特殊元素が圧延開始時に鋼中に固溶して
いる必要がある為にスラブは高温(〜1250℃)に
加熱される。しかし、本発明では仕上圧延開始時
に鋼中に析出物が存在している必要がある。特殊
元素が一旦スラブに固溶してしまうと、粗圧延で
その一部が析出するものの、本発明の効果が発揮
される程ではなく、逆に固溶元素が変態を抑制す
る為に最終的なフエライト粒径は超微細なものに
はならない。添加特殊元素(Ti,NbおよびTa)
が仕上圧延開始時に十分析出しているにはスラブ
加熱温度が1100℃を超えてはならない。そこでス
ラブ加熱温度を1100℃以下に限定した。また本発
明の趣旨から加熱温度がAc3(加熱変態点)以上
である事は当然である。 このように加熱されたスラブを熱間圧延する
が、この圧延温度がAr3(冷却変態点)以下にな
ると加工を加えなくともフエライトが生成する
が、この様なフエライト粒径は大きいために、
かゝる組織が加工を受けると回復が遅く延性及び
靭性を著しく損なう。一方加工により誘起したフ
エライトは超微細であり生成後に更に加工を受け
ても容易に回復・再結晶する。 圧延温度が高いと加工により誘起するフエライ
トの量が少く、十分な量を得るには実現不可能な
圧下率を必要とする。現実的な圧延設備に於て十
分な量の微細フエライトを得るには仕上温度が
Ar3+100℃以下になる様な圧延温度が望ましい。
第1図は0.047%Nbを含有した鋼のスラブ加熱温
度と加工温度のフエライト組織に及ぼす効果を示
したもので、1050℃の加熱温度で加工温度が約
730℃(Ar3点)より約850℃の温度範囲がフエラ
イト粒度No.が大きく、フエライト変態量が多いこ
とがわかる。以上の理由により圧延仕上温度を
Ar3〜Ar3+100℃に限定した。 なお、特殊元素のAr3変態点におよぼす効果が
必ずしも明らかでないときは、特殊元素の項を含
まない次式の計算値を便宜的にAr3とすればよ
い。 Ar3=901―325C+33Si―92Mn(℃)
(成分量はwt%) 次に、上記のような温度範囲における圧延条件
について説明する。 本発明者らが以前に開示した特殊元素を含まな
い炭素鋼を用い超微細なフエライト組織を得る方
法は基本的には大圧下率による圧延であり、1パ
ス大圧下を多パスで代替する時は、前パス加工の
影響が消失しないうちに次パス加工を行なう様に
短いパス間時間を要求した。本発明によれば特殊
元素添加のためにこれらの要求が大巾に緩和さ
れ、第3図に示す如く最終パスより遡つて15秒以
内に累計圧下率50%以上の圧延を行なえば粒度番
号13.5番以上(粒径3μ以下)の超微細組織を得る
事ができる。第3図はC:0.14%,Mn:1.5%,
Nb:0.047%含有した鋼を加熱温度1000℃,圧延
温度仕上780℃で圧延し、20℃/sで400℃以下ま
で水冷した鋼の15秒以内の累計圧下率とフエライ
ト粒径の関係を示したものである。パス間時間が
長く、2〜3パスの圧延に15秒以上かかる場合
は、1パスの圧下率を大きくしなければならず実
用性に乏しくなる。そこで圧延条件を圧延最終段
で15秒以内に合計50%以上の圧下を加える様に限
定した。パス間時間が短くなれば、また圧下率が
大きくなれば粒径はより小さくなる。 次に冷却条件について説明する。 本発明鋼は加工直後の状態で超微細フエライト
組織となつているが、場合によつては加工後緩冷
により粒成長を起す場合がある。また加工直後に
オーステナイトがある比率残存する場合にはフエ
ライトが冷却中に成長する。このような場合には
急冷を行うことにより粗大化を防止することがで
きる。このとき圧延後5秒以上高温域で放置する
とその後急冷しても、上記の粗大化防止の効果は
ないので、圧延後水冷開始までの時間を5秒以内
に限定した。 第4図はC:0.14%,Mn:1.5%,Nb:0.047
%含有した鋼を加熱温度1000℃,圧延仕上温度を
780℃とし、合計圧下率85%で圧延したあとの経
過時間とフエライト粒度No.の関係を示したもの
で、同図からも上述の如く5秒以内に水冷を開始
する必要があることがわかる。 また冷却速度は10℃/s以上でなければ、粗大
化防止の効果はないので、冷却速度は10℃/s以
上とした。上記の急冷は当然のことながらフエラ
イトを強化し、さらに加工直後残存しているオー
ステナイトをベイナイト,マルテンサイト等の強
化組織とすることにより強度上昇に効果がある
が、この目的のためには上記10℃/s以上で冷却
速度が大きいほど効果があるのは勿論である。 (実施例) 表1に示す成分の5種類の鋼を用い、表2に示
す仕上圧延のパススケジユールに従い表3の条件
で連続熱延を行なつた。鋼Aは比較材、鋼B〜E
は本発明範囲内の成分を有する。仕上圧延スケジ
ユールfは各パスとも通常の圧下率とした通常圧
延で、スケジユールgは後段パスの圧下率を大き
くとり、第1パスを空パスとした5パス圧延であ
る。 表3の試番,は特殊元素を含まないので、
圧延終了時のフエライト生成量が不十分であり、
冷却後の組織はベイナイト主体となつてしまう。
試番,は加熱温度が高温であるためにNb,
Tiが固溶し、フエライト変態を抑制するために
やはりベイナイト主体の組織である。試番は仕
上温度が高いためにフエライト生成量が十分でな
く、またフエライトの粒径もそれ程は小さくなら
ない。試番は仕上温度がAr3以下となつたため
に、フエライト粒径は微細であるものの加工フエ
ライトとなつてしまい伸びが劣化している。は
比較材の通常工程によるもので従来の組織・材質
を示す。その他の試番(※印)は本発明範囲内で
あり粒度番号は14.5〜15.5と非常に微細であり、
優秀な強度―延性バランスを示す。第5図には表
3に記してある強度(TS)と伸び(E)の積
を粒度番号に対しプロツトしたが(表中の数字は
表3の試番に対応する)、本発明による超微細鋼
の優位性が明らかである。なお、圧延圧下率は大
圧下の方がやや良い材質を示すが、通常の圧下率
でもフエライト粒は超微細であり材質も最良のも
のに対し遜色がない。 (発明の効果) 本発明により材質の優れた抗張力60Kg/mm2以上
の高張力薄鋼板を、通常の圧延設備で生産性を低
下させずに安価に製造提供する事が可能となつ
た。
(Field of Industrial Application) The present invention relates to a method for manufacturing high-tensile steel materials used for automobile strength members, wheels, welded steel pipe materials, structural members, etc. (Prior art) Among the various methods for strengthening steel, grain refinement is known as the only method to increase toughness as well as strength, and is particularly effective in improving the material quality of steel materials used as hot-rolled. It is an important technique that must be considered first in most cases when measuring. What has been achieved industrially with conventional grain refining technology is as small as 4
It is about ~6μ. This is usually carried out using a method called controlled rolling, which is a technique for strongly rolling steel containing alloying elements such as Nb at relatively low temperatures. In this case, Nb needs to be in solid solution as rolled, so heating is performed at a high temperature of 1200°C or higher before rolling to dissolve Nb, and then finish rolling is performed at a low temperature of 800°C or lower. Because it is done with
This method has industrial disadvantages, such as waiting for the temperature of the steel plate to drop, resulting in a significant drop in production efficiency, and a significant increase in deformation resistance during rolling, resulting in a heavy load on the rolling mill. In addition, various methods have been proposed, such as heating and rolling in a low temperature range or forced cooling after rolling, but in all cases the particle size remains within the above-mentioned range. Recently, carbon steel that does not contain special elements has a grain size of 3~
Method for obtaining ultrafine grains of 4μ or less
123823), but this method requires a large reduction rate during rolling and is subject to equipment limitations. (Problems to be Solved by the Invention) The present invention is capable of producing high-quality, high-strength steel material consisting of an ultrafine ferrite structure with a grain size of 3 to 4 μm or less at a low cost without reducing productivity using ordinary hot rolling equipment. With the goal. Furthermore, an ultra-fine ferrite structure is one in which the individual crystal grain size is 3 to 4 μ or less (grain size number 13 or more).
refers to a structure in which ferrite accounts for 60% or more by volume. (Means for solving the problems) The gist of the present invention is as follows. That is, by weight, it contains C: 0.05-0.2% Si: 0.01-1.0% Mn: 0.3-2.0%, and further contains one or more of Ti, Nb, and Ta, respectively.
After heating steel containing 0.01 to 0.1% Ac to a temperature of 3 points or more and 1100℃ or less, hot rolling is performed in the cooling process, and at that time, a total reduction of 50% or more is applied within 15 seconds in the final stage of rolling. Add and adjust the finishing temperature.
A method for producing ultrafine-grained, low-alloy hot-rolled high-strength steel, characterized by cooling at Ar 3 points to Ar 3 +100°C at a cooling rate of 10°C/s or more within 5 seconds after the end of hot rolling. The content of the present invention will be explained in detail below. The gist of the present invention is to cause a suitable amount of fine precipitates to be present in the steel at the start of hot rolling, and to induce ferrite transformation using these precipitates as transformation nuclei during rolling. Conventionally, it has been known that if precipitates are present when steel transforms from high-temperature austenite to ferrite by cooling, these precipitates become transformation nuclei in areas other than grain boundaries. On the other hand, the present inventors have previously shown that when a large reduction is applied to carbon steel just before the transformation from austenite to ferrite, ferrite transformation is induced and fine ferrite grains are formed. When there is an appropriate amount of , deformation-induced transformation easily occurs,
It was found that an ultrafine ferrite structure can be formed even if the pass rolling reduction is relatively small. Figure 2 is 0.15C
-1.5Mn steel with various amounts of Nb added,
The ferrite grain size after rolling with varying heating temperatures and rolling reduction ratios is shown, and it can be seen that the microstructure becomes fine even at low rolling reductions when Nb is precipitated by low-temperature heating before rolling. The structure of the present invention will be explained below, but first, the steel components will be explained. C is the main component that affects the structure and material quality of carbon steel, but if it is less than 0.05%, high strength cannot be obtained;
If it exceeds this value, transformation due to processing will be insufficient, and weldability and workability will also decrease. Therefore, 0.05%≦C≦
Limited to 0.2%. Addition of Mn is desirable as it improves the strength-toughness balance and also has the effect of refining the structure, but its effect will not appear if it is less than 0.3%, and if it exceeds 2%, the transformation point will drop too much and ferrite transformation will occur. It becomes insufficient. Therefore, it was limited to 0.3%≦Mn≦2.0%. Adding Si in an amount of 0.01% or more improves the strength-ductility balance of the steel sheet, so it is desirable to add Si.
If it exceeds %, weldability may be impaired.
It was limited to 0.01%≦Si≦1.0%. Ti, Nb and Ta are carbides (and carbonitrides)
Since it forms a transformation nucleus, it is an essential element in the present invention. If the total amount of one or more of these added is less than 0.01%, the amount of precipitates will be small and the effect will be small. Moreover, if it exceeds 0.1%, the size of the precipitates becomes inappropriate and the effect is reduced. Therefore, Ti, Nb
The total addition amount of one or more of Ta and Ta was limited to 0.01% to 0.1%. Special elements other than those listed above (such as V) are effective if they precipitate in appropriate amounts at the start of finish rolling, but Ti,
Since it does not show the same effect as Nb and Ta, it is not particularly limited. However, it may be added as a supplement. The formation temperature of precipitates is low, and elements (Mo
etc.) have no effect. Next, the manufacturing method of the present invention will be explained. In the present invention, the heating temperature of the slab, which is the rolled material, needs to be low. In conventional controlled rolling,
Because special elements such as Nb must be dissolved in the steel at the start of rolling, the slab is heated to a high temperature (~1250°C). However, in the present invention, precipitates must be present in the steel at the start of finish rolling. Once the special elements are solid-solved in the slab, some of them will precipitate during rough rolling, but this will not be enough to achieve the effects of the present invention, and on the contrary, the solid-solute elements will suppress the transformation. The ferrite grain size is not ultra-fine. Added special elements (Ti, Nb and Ta)
The slab heating temperature must not exceed 1100°C in order for the slab to be sufficiently analyzed at the start of finish rolling. Therefore, the slab heating temperature was limited to 1100℃ or less. Further, from the spirit of the present invention, it is a matter of course that the heating temperature is equal to or higher than Ac 3 (heating transformation point). The heated slab is hot-rolled, but when the rolling temperature drops below Ar 3 (cooling transformation point), ferrite is generated without further processing, but since the grain size of such ferrite is large,
When such a structure is subjected to processing, recovery is slow and ductility and toughness are significantly impaired. On the other hand, ferrite induced by processing is ultrafine and easily recovers and recrystallizes even if it is further processed after its formation. When the rolling temperature is high, the amount of ferrite induced by processing is small, and obtaining a sufficient amount requires an unrealizable reduction rate. In order to obtain a sufficient amount of fine ferrite in practical rolling equipment, the finishing temperature is
It is desirable that the rolling temperature be below Ar 3 +100°C.
Figure 1 shows the effects of slab heating temperature and processing temperature on the ferrite structure of steel containing 0.047% Nb.
It can be seen that in the temperature range from 730°C (Ar 3 points) to about 850°C, the ferrite particle size number is large and the amount of ferrite transformation is large. For the above reasons, the finishing temperature of rolling
The temperature was limited to Ar 3 to Ar 3 +100°C. Note that when the effect of the special element on the Ar 3 transformation point is not necessarily clear, the calculated value of the following formula that does not include the term of the special element may be used as Ar 3 for convenience. Ar 3 =901-325C+33Si-92Mn (℃)
(The amount of components is wt%) Next, the rolling conditions in the above temperature range will be explained. The method of obtaining an ultra-fine ferrite structure using carbon steel that does not contain special elements, which the present inventors previously disclosed, is basically rolling with a large reduction ratio, and when one pass large reduction is replaced by multiple passes. required a short interpass time so that the next pass could be performed before the effects of the previous pass disappeared. According to the present invention, these requirements are greatly relaxed due to the addition of special elements, and as shown in Figure 3, if rolling is performed at a cumulative reduction rate of 50% or more within 15 seconds from the final pass, the grain size number will be 13.5. It is possible to obtain an ultra-fine structure of grain size or larger (grain size of 3μ or less). Figure 3 shows C: 0.14%, Mn: 1.5%,
The relationship between the cumulative reduction rate within 15 seconds and the ferrite grain size of steel containing 0.047% Nb was rolled at a heating temperature of 1000°C and a finishing temperature of 780°C, and water-cooled at 20°C/s to 400°C or less. It is something that If the inter-pass time is long and it takes 15 seconds or more for two or three passes of rolling, the rolling reduction ratio for one pass must be increased, making it impractical. Therefore, the rolling conditions were limited to applying a total reduction of 50% or more within 15 seconds at the final rolling stage. The shorter the inter-pass time and the larger the rolling reduction, the smaller the grain size. Next, cooling conditions will be explained. The steel of the present invention has an ultrafine ferrite structure immediately after processing, but in some cases, grain growth may occur due to slow cooling after processing. Further, if a certain proportion of austenite remains immediately after processing, ferrite grows during cooling. In such cases, coarsening can be prevented by performing rapid cooling. At this time, if the product was left in a high temperature range for 5 seconds or more after rolling, even if it was rapidly cooled afterwards, there would be no effect of preventing the above-mentioned coarsening, so the time after rolling until the start of water cooling was limited to 5 seconds or less. Figure 4 shows C: 0.14%, Mn: 1.5%, Nb: 0.047
% steel was heated at a temperature of 1000°C and the rolling finishing temperature was
This figure shows the relationship between the elapsed time after rolling at 780°C and a total reduction rate of 85% and the ferrite particle size number, and it can be seen from the figure that water cooling must be started within 5 seconds as mentioned above. . Further, since there is no effect of preventing coarsening unless the cooling rate is 10°C/s or more, the cooling rate was set to be 10°C/s or more. The above quenching naturally strengthens the ferrite, and is also effective in increasing the strength by converting the austenite remaining after processing into a reinforcing structure such as bainite and martensite. It goes without saying that the higher the cooling rate is at C/s or higher, the more effective it is. (Example) Using five types of steels having the components shown in Table 1, continuous hot rolling was performed under the conditions shown in Table 3 according to the finish rolling pass schedule shown in Table 2. Steel A is comparative material, steel B to E
has components within the scope of this invention. The finishing rolling schedule f is normal rolling with a normal rolling reduction in each pass, and the schedule g is 5-pass rolling with a large rolling reduction in the later passes and the first pass being an empty pass. The sample number in Table 3 does not contain any special elements, so
The amount of ferrite produced at the end of rolling was insufficient,
The structure after cooling becomes mainly bainite.
The trial number is Nb because the heating temperature is high.
The structure is still mainly bainite because Ti is dissolved in solid solution and suppresses ferrite transformation. In the trial sample, the finishing temperature was high, so the amount of ferrite produced was not sufficient, and the particle size of ferrite was not reduced to that extent. Since the finishing temperature of the trial sample was below Ar 3 , the ferrite grain size was fine, but it became processed ferrite and its elongation deteriorated. indicates the conventional structure and material due to the normal process of comparative materials. Other sample numbers (marked with *) are within the scope of the present invention and have very fine particle size numbers of 14.5 to 15.5.
Exhibits excellent strength-ductility balance. In Figure 5, the product of strength (TS) and elongation (E) listed in Table 3 is plotted against the particle size number (the numbers in the table correspond to the trial numbers in Table 3). The superiority of fine steel is clear. In addition, the material quality is slightly better when the rolling reduction ratio is large, but even at a normal rolling reduction ratio, the ferrite grains are ultra-fine and the material quality is comparable to the best one. (Effects of the Invention) According to the present invention, it has become possible to manufacture and provide high-strength thin steel sheets of excellent material with a tensile strength of 60 kg/mm 2 or more at low cost without reducing productivity using ordinary rolling equipment.

【表】【table】

【表】【table】

【表】【table】

【表】【table】 【図面の簡単な説明】[Brief explanation of the drawing]

第1図は0.15C―1.5Mn鋼にNbを種々変えて添
加したものにつき、加熱温度を1250℃と1000℃、
最終パスを含んで15秒以内の圧下率を50〜85%に
変化させて圧延・冷却した時のフエライト粒度を
示す。第2図は0.14C―1.5Mn―0.047Nb鋼の加熱
温度と圧延温度が圧延後のフエライト組織におよ
ぼす効果を示す。第3図は0.14C―1.5Mn―
0.047Nb鋼を加熱温度1000℃、仕上温度780℃で
圧延し、その後20℃/sの冷速で400℃以下まで
水冷したものにつき、最終パスを含んだ15秒以内
の累計圧下率とフエライト粒度の関係を示す。第
4図は0.14C―1.5Mn―0.047Nb鋼を加熱温度1000
℃、仕上温度780℃、2パスの合計圧下率85%、
パス間時間2秒で加工し、加工後所定の時間で水
中に焼入れたものにつき、加工後の経過時間とフ
エライト粒度の関係を示す。第5図は実施例のう
ちフエライト主体の組織である鋼につき、フエラ
イト粒度と材質(強度×伸び)の関係を示す。
Figure 1 shows 0.15C-1.5Mn steel with various Nb additions at heating temperatures of 1250°C and 1000°C.
The ferrite particle size is shown when rolling and cooling is performed by changing the rolling reduction rate from 50 to 85% within 15 seconds including the final pass. Figure 2 shows the effects of heating temperature and rolling temperature on the ferrite structure after rolling of 0.14C-1.5Mn-0.047Nb steel. Figure 3 is 0.14C―1.5Mn―
Cumulative rolling reduction and ferrite grain size within 15 seconds including the final pass for 0.047Nb steel rolled at a heating temperature of 1000°C and a finishing temperature of 780°C, then water-cooled at a cooling rate of 20°C/s to below 400°C. shows the relationship between Figure 4 shows 0.14C-1.5Mn-0.047Nb steel heated to a temperature of 1000.
℃, finishing temperature 780℃, total reduction rate of 2 passes 85%,
The relationship between the elapsed time after processing and the ferrite particle size is shown for those processed with an interpass time of 2 seconds and quenched in water for a predetermined time after processing. FIG. 5 shows the relationship between ferrite grain size and material quality (strength x elongation) for steel with a ferrite-based structure among Examples.

Claims (1)

【特許請求の範囲】 1 重量で、 C:0.05〜0.2% Si:0.01〜1.0% Mn:0.3〜2.0% を含み、さらに、 Ti,Nb,Taの1種または2種以上をそれぞれ
0.01〜0.1%含有する鋼を、Ac3点以上1100℃以下
の温度に加熱した後、冷却過程において熱間圧延
を行ない、その際、圧延最終段で15秒間以内に合
計50%以上の圧下を加えるとともに仕上温度を
Ar3点〜Ar3+100℃とし、熱間圧延終了後5秒間
以内に10℃/s以上の冷却速度で冷却することを
特徴とする超細粒低合金熱延高張力鋼の製造方
法。
[Claims] 1. Contains, by weight, C: 0.05-0.2% Si: 0.01-1.0% Mn: 0.3-2.0%, and further contains one or more of Ti, Nb, and Ta, respectively.
After heating steel containing 0.01 to 0.1% Ac to a temperature of 3 points or more and 1100℃ or less, hot rolling is performed in the cooling process, and at that time, a total reduction of 50% or more is applied within 15 seconds in the final stage of rolling. Add and adjust the finishing temperature.
A method for producing ultrafine-grained, low-alloy hot-rolled high-strength steel, characterized by cooling at Ar 3 points to Ar 3 +100°C at a cooling rate of 10°C/s or more within 5 seconds after the end of hot rolling.
JP17418684A 1984-08-23 1984-08-23 Manufacture of ultrafine grain low alloyed hot rolled high tensile steel Granted JPS6156233A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP17418684A JPS6156233A (en) 1984-08-23 1984-08-23 Manufacture of ultrafine grain low alloyed hot rolled high tensile steel

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP17418684A JPS6156233A (en) 1984-08-23 1984-08-23 Manufacture of ultrafine grain low alloyed hot rolled high tensile steel

Publications (2)

Publication Number Publication Date
JPS6156233A JPS6156233A (en) 1986-03-20
JPS647130B2 true JPS647130B2 (en) 1989-02-07

Family

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Family Applications (1)

Application Number Title Priority Date Filing Date
JP17418684A Granted JPS6156233A (en) 1984-08-23 1984-08-23 Manufacture of ultrafine grain low alloyed hot rolled high tensile steel

Country Status (1)

Country Link
JP (1) JPS6156233A (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA2004548C (en) * 1988-12-05 1996-12-31 Kenji Aihara Metallic material having ultra-fine grain structure and method for its manufacture
CZ299495B6 (en) * 2005-12-06 2008-08-13 Comtes Fht, S. R. O. A method of producing high strength low alloy steel pipes

Also Published As

Publication number Publication date
JPS6156233A (en) 1986-03-20

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