JPH0534403B2 - - Google Patents
Info
- Publication number
- JPH0534403B2 JPH0534403B2 JP6482984A JP6482984A JPH0534403B2 JP H0534403 B2 JPH0534403 B2 JP H0534403B2 JP 6482984 A JP6482984 A JP 6482984A JP 6482984 A JP6482984 A JP 6482984A JP H0534403 B2 JPH0534403 B2 JP H0534403B2
- Authority
- JP
- Japan
- Prior art keywords
- forging
- quenching
- temperature
- less
- steel
- 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 - Lifetime
Links
- 229910000831 Steel Inorganic materials 0.000 claims description 33
- 238000005242 forging Methods 0.000 claims description 33
- 239000010959 steel Substances 0.000 claims description 33
- 238000010791 quenching Methods 0.000 claims description 31
- 230000000171 quenching effect Effects 0.000 claims description 29
- 239000000463 material Substances 0.000 claims description 19
- 238000010438 heat treatment Methods 0.000 claims description 11
- 229910052782 aluminium Inorganic materials 0.000 claims description 6
- 229910052804 chromium Inorganic materials 0.000 claims description 6
- 238000004519 manufacturing process Methods 0.000 claims description 6
- 230000001105 regulatory effect Effects 0.000 claims description 4
- 229910052757 nitrogen Inorganic materials 0.000 claims description 3
- 229910052799 carbon Inorganic materials 0.000 claims 1
- 229910052698 phosphorus Inorganic materials 0.000 claims 1
- 229910001566 austenite Inorganic materials 0.000 description 11
- 238000009826 distribution Methods 0.000 description 7
- 238000000034 method Methods 0.000 description 7
- 238000005275 alloying Methods 0.000 description 6
- 238000005336 cracking Methods 0.000 description 6
- 239000000203 mixture Substances 0.000 description 6
- 229910052750 molybdenum Inorganic materials 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- 238000005496 tempering Methods 0.000 description 5
- 239000003795 chemical substances by application Substances 0.000 description 2
- 238000007796 conventional method Methods 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 229910045601 alloy Inorganic materials 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 229910052745 lead Inorganic materials 0.000 description 1
- 229910052758 niobium Inorganic materials 0.000 description 1
- 238000004881 precipitation hardening Methods 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 238000003303 reheating Methods 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 238000007711 solidification Methods 0.000 description 1
- 230000008023 solidification Effects 0.000 description 1
- 238000009864 tensile test Methods 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 229910052720 vanadium Inorganic materials 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21D—MODIFYING 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
- C21D1/00—General methods or devices for heat treatment, e.g. annealing, hardening, quenching or tempering
- C21D1/02—Hardening articles or materials formed by forging or rolling, with no further heating beyond that required for the formation
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)
Description
本発明は直接焼入れ熱間鍛造品の製造方法に関
する。
従来、高強度を要求される自動車や建設機械に
用いられる機械構造用部品は、鋼材を熱間鍛造し
た後、再加熱し、焼入れ焼戻し等の調質処理を施
して、目的、用途に応じた強度特性を付与して製
造され、使用に供されている。このように、鍛造
後に上記熱処理を行なう方法においては、用いる
鋼材には、焼入れ性を確保するためにCrやMoの
ような合金元素が添加されており、更に、オース
テナイト結晶粒を微細化して、焼入れ焼戻し後の
靭性を確保するために、Al、Nb、Ti、V等の析
出硬化型合金元素が添加されている。
しかし、熱間鍛造後の上記熱処理は、必然的に
処理工程の増加と仕掛り品の増大を伴うと共に、
多大のエネルギー費用を要し、更に、用いる鋼材
には上記のように種々の合金元素を添加する必要
があるために、製造費用が高くならざるを得な
い。
このために、近年、製造費用を低減すると共
に、工程を簡略化するために、高価な合金元素の
添加量を極力減らした鋼材を熱間鍛造後に直接焼
入れして鍛造品を得る方法が要望されるに至つて
いる。しかし、上記したような鋼材を熱間鍛造後
に直接焼入れするとき、鍛造前の加熱温度や鍛造
条件によつて、鍛造品は焼入れ後の硬さにばらつ
きを生じる。即ち、上記したような合金元素を含
有する鋼材を、例えば1250℃のように高温に加熱
して鍛造すれば、鋼材は高温加熱によつてオース
テナイト粒が粗大化し、次いで、熱間鍛造によつ
て細粒化するものの、その後に直ちに成長して再
び粗大化するので、鍛造後に直性焼入れしても焼
入れ性は良好である。しかし、鍛造温度が1050℃
以下に低下した場合や、鍛造を繰り返した場合
は、オーステナイト粒は均一な粗粒に成長せず、
細粒の混入した混粒になり、従つて、鍛造後に直
接焼入れすると、鍛造品は焼入れ性の不均一が生
じ、硬さが十分に高くならない位置が生じて、硬
さむらを生じる。
このような硬さむらの発生を避けるために、従
来は、鋼材を鍛造前に1200℃以上の高温に加熱す
ると共に、鍛造後の焼入れもできる限り高い温度
から開始されている。しかし、高温鍛造によれば
ダイス寿命が短くなり、また、焼入れ前に酸化物
層が形成され、表面部に焼きむらを発生する問題
もある。
本発明者らは上記した問題を解決するために鋭
意研究した結果、鋼材における化学組成につい
て、特にAlとNの量を規制すると共に、鍛造前
の加熱温度と焼入れ温度を所定の範囲とすること
により、熱間鍛造後に直接焼入れして、焼入れ性
が良好で且つ均一な鍛造品を得ることができるこ
とを見出して、本発明に至つたものである。
本発明による直接焼入れ鍛造品の製造方法は、
重量%で
C 0.26〜0.50%、
Si 0.50%以下及び
Mn 0.30〜1.8%を含有し、
P 0.020%以下、
S 0.01〜0.2%、
Al 0.006%以下及び
N 0.005%以下に規制した鋼材を900〜1200℃
の温度に加熱した後に鍛造し、次いで、850℃以
上の温度で焼入れすることを特徴とする。
先ず、本発明の方法において素材鋼として用い
る鋼材の組成の限定理由を説明する。
Cは、熱間鍛造後の直接焼入れ焼戻し処理によ
つて鍛造品の強度を確保するために必要不可欠の
元素として添加されるが、その含有量が0.26%未
満ではかかる強度効果に乏しく、一方、0.50%を
越えるときは、鍛造後の直接焼入れ時の焼き割れ
や置割れを生じる。従つて、Cの添加量範囲は
0.26〜0.50%とする。
Siは脱酸のために添加されるが、過多に添加す
るときは延性を劣化させる。従つて、Siの添加量
範囲は0.5%以下とする。
Mnは凝固時の表面割れを防止のために少なく
とも0.3%を添加することが必要であり、更に、
焼入れ性を改善し、また、強度を高めるのに効果
がある。しかし、1.8%を越えて多量に含有させ
ると、焼き割れの原因にもなるので、その上限は
1.8%とする。
Pは鋼材の延性を劣化させ、焼き割れを助長
し、焼戻し時の靱性を劣化させるために、含有量
は0.020%以下とする。
Sは鍛造品の被削性を改善するために有効であ
るが、反面、延性を低下させる。従つて、延性が
重要であるときは、上限は0.03%が好ましく、被
削性が重要であるときは、その上限を0.20%とす
る。
Alは強力な脱酸剤として添加されるが、0.006
%を越えて添加するときは、鍛造後の焼入れ時に
オーステナイト粒の混粒を生じて、焼きむらを発
生させることがあるので、上限を上記のように
0.006%とする。
NはAlと結合力が強いために、鋼中に多量に
含有されるとは、脱酸剤としてのAlと結合し、
やはり鍛造後の焼入れ時にオーステナイト混粒を
生じる結果、焼きむらを生じさせる。このため、
本発明においては、N量は0.006%以下とする。
更に、本発明において用いる素材鋼は、例え
ば、鍛造品の表面硬化を行なう場合の焼入れ性を
増す等、機械的性質の種々の改善のために、必要
に応じてCr及びMoから選ばれる少なくとも1種
を添加することができる。これら元素の添加量の
上限は、Cr及びMoについてそれぞれ1.2%及び
0.3%とする。これらの添加量がそれぞれ上記上
限を越えるときは、焼き割れを生じるからであ
る。また、鍛造品の被削性を改善するために、前
記したSと共に、又はSに代えてPbを0.05〜0.30
%の範囲で添加してもよい。
本発明によれば、特に鋼におけるAlとNの量
を微量に抑えることにより、鋼を熱間鍛造後焼入
れ時にオーステナイト粒の混粒が生じて焼きむら
を生じるのを未然に防止することができたので、
900〜1200℃の温度に加熱した後に鍛造し、次い
で、850℃以上の温度で焼入れし、常法に従つて
450〜650℃程度で焼戻しすれば、焼入れ性が良好
均一で、且つ、靭性にすぐれた鍛造品を得ること
ができる。焼入れ温度が850℃よりも低いときは
焼入れ性が低下し、焼むらを生じることがあるの
で好ましくない。
従来の鋼材を用いる場合には、1100〜1000℃の
温度範囲で鍛造し、直接焼入れすれば、オーステ
ナイト粒が混粒化し、焼きむらが生じて、焼入れ
が均一に入らず、一方、1000℃以下の低温で鍛造
した後に直性焼入れすれば、オーステナイト粒が
細粒化して、焼入れ性が劣化するのに対して、本
発明によれば、1100〜900℃のような低温にて鍛
造をすることができて、しかも、焼入れ性が良好
且つ均一である鍛造品を得ることができる。更
に、本発明の方法によれば、使用する素材鋼には
高価な合金元素の添加を要せず、又は特に焼入れ
性を高めるために極く少量の合金元素を添加すれ
ば足りるので、素材費用も低減される。
以下に実施例を挙げて本発明を説明する。
実施例 1
第1表A〜Fに示す化学組成を有する30mm径棒
鋼を900℃、1000℃、1100℃又は1200℃に加熱し
た後、20mm径に型鍛造し、次いで、それぞれ860
℃、920℃、950℃及び1030の温度から水冷して、
得られた鍛造品について横断面の硬さ分布を測定
した。結果を第1図に示す。本発明鋼によれば、
鍛造後、直ちにオーステナイト結晶粒が粗大化す
るために、鍛造前の加熱温度が低くとも、鍛造後
の焼入れ性が良好であつて、中心部までよく焼入
れされている。しかし、Al量が本発明で規定す
る量よりも多い従来鋼によれば、鍛造前の加熱温
度がそれぞれ900℃、1000℃及び1100℃であると
きは焼入れ時にオーステナイト粒が細粒に、ま
た、1200℃であるときは混粒になり、一方、N量
が本発明で規定する量よりも多い比較鋼は900℃
に加熱したときは細粒に、また、それ以上の高い
温度に加熱したときは混粒になるため、これらの
場合には鍛造後の焼入れ性が著しく不均一であ
る。
次に第1表A〜Dに示す化学組成を有する40mm
径の棒鋼を1000℃に加熱し、25mm径に型鍛造した
後、900℃の温度から水冷し、引張強さが同じに
なるように、本発明鋼は500℃で、従来鋼と比較
鋼は420℃で2時間焼戻しした。このようにして
得た各鍛造品より引張試験片とシヤルピー試験片
を丸棒中央より採取し、試験した。結果を第2表
に示す。強度が同等の場合、本発明鋼は靭性がす
ぐれている。
実施例 2
第1表E及びFに示す化学組成を有する75mm角
材を1050℃に加熱し、50mm径棒鋼に熱間鍛造した
後、950℃の温度から油焼入れ後、横断面の硬さ
分布を測定した。結果を第2図に示す。
Cr及びMoを添加して焼入れ性を改善した鋼
The present invention relates to a method for producing a directly quenched hot forged product. Conventionally, mechanical structural parts used in automobiles and construction machinery that require high strength have been produced by hot forging steel materials, then reheating, and then undergoing heat treatment such as quenching and tempering to meet the needs of the purpose and use. It is manufactured and put into use with added strength properties. In this way, in the method of performing the above-mentioned heat treatment after forging, alloying elements such as Cr and Mo are added to the steel material used to ensure hardenability, and the austenite crystal grains are further refined. In order to ensure toughness after quenching and tempering, precipitation hardening alloy elements such as Al, Nb, Ti, and V are added. However, the above heat treatment after hot forging inevitably involves an increase in processing steps and an increase in work in progress, and
This requires a large amount of energy, and furthermore, it is necessary to add various alloying elements to the steel material used, as described above, which inevitably increases manufacturing costs. For this reason, in recent years, in order to reduce manufacturing costs and simplify the process, there has been a demand for a method to obtain forged products by directly quenching steel materials with as little added amount of expensive alloying elements as possible after hot forging. It has reached the point where However, when directly quenching the above-mentioned steel material after hot forging, the hardness of the forged product after quenching varies depending on the heating temperature and forging conditions before forging. In other words, if a steel material containing the above alloying elements is heated to a high temperature such as 1250°C and forged, the austenite grains of the steel material become coarse due to the high temperature heating, and then the austenite grains of the steel material become coarse due to the hot forging. Although the grains become fine, they immediately grow and become coarse again, so the hardenability is good even if straight hardening is performed after forging. However, the forging temperature is 1050℃
If the drop is below or if forging is repeated, the austenite grains will not grow into uniform coarse grains,
If the forged product is quenched directly after forging, the hardenability of the forged product will be non-uniform, resulting in areas where the hardness is not sufficiently high, resulting in uneven hardness. In order to avoid such uneven hardness, conventionally, steel materials are heated to a high temperature of 1200°C or higher before forging, and quenching after forging is also started at the highest possible temperature. However, high-temperature forging shortens the life of the die, and there is also the problem that an oxide layer is formed before quenching, resulting in uneven quenching on the surface. As a result of intensive research to solve the above-mentioned problems, the inventors of the present invention found that the chemical composition of the steel material should be regulated, especially the amounts of Al and N, and the heating temperature and quenching temperature before forging should be within a predetermined range. The inventors have discovered that a forged product with good hardenability and uniformity can be obtained by directly quenching after hot forging, leading to the present invention. The method for manufacturing a direct quenched forged product according to the present invention includes:
Steel materials containing C 0.26 to 0.50%, Si 0.50% or less, and Mn 0.30 to 1.8% in weight percent, regulated to P 0.020% or less, S 0.01 to 0.2%, Al 0.006% or less, and N 0.005% or less 1200℃
It is characterized by being forged after being heated to a temperature of 850°C or higher, and then quenched at a temperature of 850°C or higher. First, the reasons for limiting the composition of the steel material used as the steel material in the method of the present invention will be explained. C is added as an essential element to ensure the strength of forged products through direct quenching and tempering treatment after hot forging, but if its content is less than 0.26%, this strength effect is poor; When it exceeds 0.50%, quench cracking or placement cracking occurs during direct quenching after forging. Therefore, the range of addition amount of C is
Set to 0.26-0.50%. Si is added for deoxidation, but when added in excess, it deteriorates ductility. Therefore, the amount of Si added should be 0.5% or less. It is necessary to add at least 0.3% of Mn to prevent surface cracking during solidification, and
It is effective in improving hardenability and increasing strength. However, if the content exceeds 1.8%, it may cause cracking, so the upper limit is
The rate shall be 1.8%. Since P deteriorates the ductility of the steel material, promotes quench cracking, and deteriorates the toughness during tempering, the content is set to 0.020% or less. S is effective for improving the machinability of forged products, but on the other hand, it reduces ductility. Therefore, when ductility is important, the upper limit is preferably 0.03%, and when machinability is important, the upper limit is 0.20%. Al is added as a strong deoxidizing agent, but 0.006
If it is added in excess of %, austenite grains may be mixed during quenching after forging, resulting in uneven quenching, so the upper limit should be set as above.
It shall be 0.006%. N has a strong bonding force with Al, so if it is contained in large amounts in steel, it will bond with Al as a deoxidizing agent.
After all, mixed austenite grains are produced during quenching after forging, resulting in uneven quenching. For this reason,
In the present invention, the amount of N is 0.006% or less. Furthermore, the material steel used in the present invention may optionally contain at least one member selected from Cr and Mo in order to improve various mechanical properties, such as increasing hardenability when surface hardening a forged product. Seeds can be added. The upper limit of the addition amount of these elements is 1.2% and 1.2% for Cr and Mo, respectively.
Set at 0.3%. This is because if the amounts added exceed the above-mentioned upper limits, quench cracking will occur. In addition, in order to improve the machinability of forged products, Pb is added in an amount of 0.05 to 0.30 in addition to or in place of S.
It may be added within a range of %. According to the present invention, by suppressing the amounts of Al and N in the steel to a very small amount, it is possible to prevent uneven quenching caused by mixed grains of austenite grains during quenching of the steel after hot forging. So,
Forged after heating to a temperature of 900-1200℃, then quenched at a temperature of 850℃ or higher, and then processed according to conventional methods.
By tempering at about 450 to 650°C, a forged product with good and uniform hardenability and excellent toughness can be obtained. When the quenching temperature is lower than 850°C, the quenching property is lowered and uneven quenching may occur, which is not preferable. When using conventional steel materials, if they are forged in the temperature range of 1100 to 1000℃ and then directly quenched, the austenite grains become mixed and uneven quenching occurs, resulting in uneven quenching; If direct quenching is performed after forging at a low temperature of 1,100 to 900 degrees Celsius, the austenite grains will become finer and the hardenability will deteriorate, but according to the present invention, forging can be performed at a low temperature of 1100 to 900 degrees Celsius. Furthermore, a forged product with good and uniform hardenability can be obtained. Furthermore, according to the method of the present invention, it is not necessary to add expensive alloying elements to the raw material steel used, or it is sufficient to add a very small amount of alloying elements especially to improve hardenability, so the material cost is reduced. is also reduced. The present invention will be explained below with reference to Examples. Example 1 A 30 mm diameter steel bar having a chemical composition shown in Table 1 A to F is heated to 900°C, 1000°C, 1100°C or 1200°C, then die forged to a diameter of 20mm, and then
Water cooling from temperatures of 920℃, 950℃ and 1030℃,
The hardness distribution in the cross section of the obtained forged product was measured. The results are shown in Figure 1. According to the steel of the present invention,
Since the austenite crystal grains coarsen immediately after forging, even if the heating temperature before forging is low, the hardenability after forging is good, and the core is well hardened. However, according to conventional steels in which the amount of Al is greater than the amount specified in the present invention, when the heating temperature before forging is 900°C, 1000°C, and 1100°C, the austenite grains become fine during quenching, and When the temperature is 1200℃, the grains become mixed, while in comparison steel, where the amount of N is higher than the amount specified in the present invention, the temperature is 900℃.
When heated to a temperature higher than that, it becomes fine grains, and when heated to a higher temperature, it becomes mixed grains, so in these cases, the hardenability after forging is significantly non-uniform. Next, 40 mm having the chemical composition shown in Table 1 A to D
A steel bar with a diameter of It was tempered at 420°C for 2 hours. A tensile test piece and a Shapey test piece were taken from the center of each round bar from each of the forged products thus obtained and tested. The results are shown in Table 2. When the strength is equivalent, the steel of the present invention has excellent toughness. Example 2 A 75 mm square bar having the chemical composition shown in Table 1 E and F was heated to 1050°C, hot forged into a 50mm diameter steel bar, and then oil quenched at a temperature of 950°C to determine the hardness distribution in the cross section. It was measured. The results are shown in Figure 2. Steel with improved hardenability by adding Cr and Mo
【表】【table】
【表】
を用いる本発明の方法によれば、鍛造焼入れの際
の焼入れ性が更に改善されている。
実施例 3
第1表G及びHに示す化学組成により快削性を
与えた30mm角材を1000℃に加熱し、20mm径棒鋼に
加熱鍛造した後、900℃の温度から水冷した後、
横断面の硬さ分布を測定した。結果を第3図に示
す。According to the method of the present invention using [Table], the hardenability during forging and hardening is further improved. Example 3 A 30 mm square piece with free machinability given the chemical composition shown in Table 1 G and H was heated to 1000°C, heated and forged into a 20 mm diameter steel bar, and then cooled with water from a temperature of 900°C.
The hardness distribution in the cross section was measured. The results are shown in Figure 3.
第1図イは本発明により得られた直接焼入れ鍛
造品の硬さ分布を示すグラフ、ロは従来の方法に
より得られた直接鍛造品についての同様のグラフ
であり、横軸は鍛造品の中心からの距離を示す。
第2図はCr及びMoを含む鋼を1050℃で鍛造後直
接焼入れした鍛造品の硬さ分布を示すグラフ、第
3図はS及びPbを含む鋼を1000℃で熱間鍛造後
直接焼入れした鍛造品の硬さ分布を示すグラフで
ある。
Figure 1 A is a graph showing the hardness distribution of a directly quenched forged product obtained by the present invention, B is a similar graph for a directly forged product obtained by a conventional method, and the horizontal axis is the center of the forged product. Indicates distance from.
Figure 2 is a graph showing the hardness distribution of a forged product made by directly quenching a steel containing Cr and Mo at 1050°C, and Fig. 3 is a graph showing the hardness distribution of a forged product made by directly quenching a steel containing S and Pb at 1000°C after hot forging. It is a graph showing the hardness distribution of a forged product.
Claims (1)
の温度に加熱した後に鍛造し、次いで、850℃以
上の温度で焼入れすることを特徴とする直接焼入
れ熱間鍛造品の製造方法。 2 C 0.26〜0.50%、 Si 0.50%以下、 Mn 0.30〜1.8%、 Cr1.2%以下及びMo0.3%以下から選ばれる少
なくとも1種を含有し、 P 0.020%以下、 S 0.01〜0.2%、 Al 0.006%以下及び N 0.005%以下に規制した鋼材を900〜1200℃
の温度に加熱した後に鍛造し、次いで、850℃以
上の温度で焼入れすることを特徴とする直接焼入
れ熱間鍛造品の製造方法。[Claims] Contains 0.26-0.50% C, 0.50% Si or less, and 0.30-1.8% Mn in 1% by weight, P 0.020% or less, S 0.01-0.2%, Al 0.006% or less, and N 0.005% or less. Steel materials regulated to 900 to 1200℃
A method for producing a directly quenched hot forged product, which is characterized by forging after heating to a temperature of 850°C or higher, and then quenching at a temperature of 850°C or higher. 2 Contains at least one selected from C 0.26 to 0.50%, Si 0.50% or less, Mn 0.30 to 1.8%, Cr 1.2% or less, and Mo 0.3% or less, P 0.020% or less, S 0.01 to 0.2%, Steel materials regulated to less than 0.006% Al and less than 0.005% N at 900 to 1200℃
A method for producing a directly quenched hot forged product, which is characterized by forging after heating to a temperature of 850°C or higher, and then quenching at a temperature of 850°C or higher.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP6482984A JPS60208414A (en) | 1984-03-31 | 1984-03-31 | Manufacture of directly-hardened hot-forged article |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP6482984A JPS60208414A (en) | 1984-03-31 | 1984-03-31 | Manufacture of directly-hardened hot-forged article |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS60208414A JPS60208414A (en) | 1985-10-21 |
| JPH0534403B2 true JPH0534403B2 (en) | 1993-05-24 |
Family
ID=13269522
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP6482984A Granted JPS60208414A (en) | 1984-03-31 | 1984-03-31 | Manufacture of directly-hardened hot-forged article |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS60208414A (en) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP3300500B2 (en) * | 1993-10-12 | 2002-07-08 | 新日本製鐵株式会社 | Method for producing hot forging steel excellent in fatigue strength, yield strength and machinability |
| JP3739958B2 (en) * | 1999-03-09 | 2006-01-25 | 新日本製鐵株式会社 | Steel with excellent machinability and its manufacturing method |
| JP3954751B2 (en) * | 1999-04-02 | 2007-08-08 | 新日本製鐵株式会社 | Steel with excellent forgeability and machinability |
| JP5268225B2 (en) * | 2005-10-07 | 2013-08-21 | トピー工業株式会社 | Method for manufacturing roller shell of lower traveling body of construction machine |
-
1984
- 1984-03-31 JP JP6482984A patent/JPS60208414A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS60208414A (en) | 1985-10-21 |
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