JPS6119687B2 - - Google Patents
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- Publication number
- JPS6119687B2 JPS6119687B2 JP55181336A JP18133680A JPS6119687B2 JP S6119687 B2 JPS6119687 B2 JP S6119687B2 JP 55181336 A JP55181336 A JP 55181336A JP 18133680 A JP18133680 A JP 18133680A JP S6119687 B2 JPS6119687 B2 JP S6119687B2
- Authority
- JP
- Japan
- Prior art keywords
- strength
- rolling
- stainless steel
- workability
- steel
- Prior art date
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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
- C21D8/00—Modifying the physical properties of ferrous metals or ferrous alloys by deformation combined with, or followed by, heat treatment
- C21D8/02—Modifying the physical properties of ferrous metals or ferrous alloys by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips
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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 Sheet Steel (AREA)
Description
本発明は高強度ステンレス鋼板の製造方法に関
するものである。
近年、省エネルギーの観点から、自動車、電車
等の輸送機関の軽量化が進められてきている。特
に、車輛においては、冷房設備、相互乗入れによ
る器材の増加等により車重増加の傾向にあり、車
体の重量軽減は重要な問題になつている。
材料の高強度化、高耐食性化による板厚減少は
輸送機関の軽量化の有力な手段である。これらの
材料は車体製造時に複雑な加工や溶接が施される
ため、高強度、高耐食性と同時に加工性、溶接性
(溶接部の強度、腐食特性等を含む。)も要求され
ることになる。特に、材料を高強度化した場合、
加工性の劣化が顕著になるが、このような現象は
一般に避けられない問題である。このため、その
用途別に、強度を重視した材料と加工性を重視し
た材料とを使いわける事が必要である。常温で加
工した際に加工誘起マルテンサイトを生じ、高強
度化する不安定オーステナイト系ステンレス鋼
は、その加工率を変える事により生成するマルテ
ンサイトの量を変化させ、強度水準を容易に変え
る事ができる。さらに、ステンレス鋼の本来所有
する高耐食性を考慮した場合、上記の要求に最も
適した材料といえる。
従来工業的にオーステナイト系ステンレス鋼を
用いて高強度ステンレス鋼板を製造する際には、
固溶化熱処理後、調質圧延を行なつていた。すな
わち、調質圧延時の圧下率を変化させる事により
任意の高強度を有する材料の製造が可能である。
しかし、単に調質圧延の圧下率の最適条件を選定
しただけでは、望ましい強度は得られても加工性
や耐食性が劣る等の問題があつた。特に、高強度
でかつ加工性が要求される場合には降伏比(σ0.
2/σB)が低く破断伸び(El)の高い材料が要求
され、従来の製造法ではこのような材料を安定し
て製造することができなかつた。
本発明は調質圧延後の強度、延性のバランス、
さらに粒界腐食等を考慮し、オーステナイト系ス
テンレス鋼の成分範囲として、C;0.04〜0.07
%、N;0.05〜0.15%、Si;1.0%以下、Mn;0.3
〜2.0%、Ni;6.0〜8.0%、Cr;16.0〜20.0%を含
有し、残部はFeおよび製鋼上不可避の元素から
なるステンレス鋼を用い、固溶化熱処理し、900
〜500℃の間を10℃/sec以上100℃/sec以下の平均
冷却速度で冷却した後、ロールギヤツプにおける
材料温度を30〜50℃に保持し調質圧延時の圧下率
を下記表に示すような値に選定する事により、
0.2%耐力が50Kg/mm2級、60Kg/mm2級、80Kg/mm2
級の加工性に優れた高強度ステンレス鋼板の製造
を可能にしたものである。
The present invention relates to a method for manufacturing a high strength stainless steel plate. In recent years, from the perspective of energy conservation, efforts have been made to reduce the weight of transportation vehicles such as automobiles and trains. Particularly, in vehicles, there is a tendency for the weight of vehicles to increase due to the increase in air conditioning equipment, equipment due to mutual access, etc., and reducing the weight of the vehicle body has become an important issue. Reducing plate thickness by increasing the strength and corrosion resistance of materials is an effective means of reducing the weight of transportation vehicles. These materials are subjected to complex processing and welding during car body manufacturing, so they are required to have high strength and high corrosion resistance, as well as workability and weldability (including strength of welded parts, corrosion characteristics, etc.). . In particular, when the material is made with high strength,
Although the deterioration of workability becomes noticeable, such a phenomenon is generally an unavoidable problem. For this reason, it is necessary to use materials that place emphasis on strength and materials that place emphasis on workability depending on the application. Unstable austenitic stainless steel produces deformation-induced martensite when processed at room temperature, increasing its strength. By changing the processing rate, the amount of martensite produced can be changed, and the strength level can be easily changed. can. Furthermore, when considering the high corrosion resistance inherent in stainless steel, it can be said that it is the most suitable material to meet the above requirements. Conventionally, when manufacturing high-strength stainless steel sheets using austenitic stainless steel,
After solution heat treatment, temper rolling was performed. That is, by changing the reduction ratio during skin pass rolling, it is possible to manufacture a material having arbitrary high strength.
However, simply selecting the optimum conditions for the rolling reduction of skin pass rolling has problems such as poor workability and corrosion resistance even though desired strength can be obtained. In particular, when high strength and workability are required, the yield ratio (σ 0 .
2 /σ B ) and high elongation at break (El) are required, and conventional manufacturing methods have not been able to stably produce such materials. The present invention provides a balance between strength and ductility after temper rolling,
Furthermore, considering intergranular corrosion, etc., the composition range of austenitic stainless steel is C; 0.04 to 0.07.
%, N; 0.05-0.15%, Si; 1.0% or less, Mn; 0.3
~2.0%, Ni: 6.0~8.0%, Cr: 16.0~20.0%, with the balance consisting of Fe and other elements unavoidable in steelmaking.
~500℃ at an average cooling rate of 10℃/sec to 100℃/sec, maintain the material temperature in the roll gap at 30 to 50℃, and reduce the reduction rate during skin pass rolling as shown in the table below. By selecting a value that is
0.2% proof stress is 50Kg/mm 2nd grade, 60Kg/mm 2nd grade, 80Kg/mm 2
This makes it possible to manufacture high-strength stainless steel sheets with superior workability.
【表】
初めに機械的性質に対する一般的な成分の影響
を示し、それから各成分の限定理由を説明する。
第1図は強度に対する成分の影響を示したもので
45Kg鋼塊から公知の冷延、焼鈍により1.1〜0.8mm
厚の鋼板とした後、0.8mm厚まで調質圧延機にて
調質圧延した材料について測定したものである。
同図のように、Cは0.2%耐力を増加させ、低強
度側で引張強さを減少させる。しかし、高強度側
ではCが低いほど引張強さは減少し、Cが0.04%
未満では特に顕著である。NはCと同様、0.2%
耐力を増加させ、引張強さを減少させる。その効
果はCより大きい。Niは0.2%耐力に影響を示さ
ないが、引張強さを顕著に減少させる。
Cr、MnはNiと同様の傾向を示すが、その効果
はNiの半分である。第2図は破断伸びに対する
成分の影響を総合的にまとめたもので製造工程は
第1図の場合と同様で、C0.02〜0.15%、Mn1〜
2%、Ni6〜9%、Cr15〜18%、N0.02〜0.2%の
ものについて測定を行なつた。図に示すように1/
2Mn+Ni−1/12(20−Cr)2+15(C+N)(%)
が大きくなるにしたがい伸びは増加する。以上の
ように、各成分とも伸びを増大させ、C、N以外
の合金元素は引張強さを顕著に減少させる。その
結果降伏比の増大をまねく。強度、延性のバラン
スを最良にするにはC、Nおよびその他の合金元
素の割合を十分コントロールする事が肝要であ
る。
以上の事実をもとに各種成分の限定理由を説明
する。
Cはオーステナイト相を安定化し、加工誘起マ
ルテンサイト相の生成を抑制する一方、オーステ
ナイト相及び生成したマルテンサイト相を固溶強
化する働きがあり、強度的には多い方が有利であ
る。Cが0.04%未満になると、マルテンサイト相
を過剰に生成させないと高強度が得られなくなり
延性の劣化をきたす。一方、C量の上限は粒界腐
食感受性から規制した。即ち第3図はC量の異な
る材料について900℃から500℃の間の冷却速度を
変化させ、10%蓚酸電解エツチテストを行つた結
果である。同図に示すようにCが0.07%を越える
と粒界腐食感受性が敏感になることがわかる。こ
のためCの範囲を0.04〜0.07%とした。
NはCと同様の働きがあり、強度的には多い方
が有利であるが、0.15%を越えるとブローホール
の発生原因となり、0.05%未満ではオーステナイ
ト相が不安定になりすぎる。このためNの範囲を
0.05〜0.15%とした。
Siは脱酸剤として製鋼上必要であるが、1.0%
を越えるとフエライト形成能が強くなり、熱間加
工性を劣化させるため1.0%を上限とした。
Mnはオーステナイト相を安定にする元素であ
り、0.3%に未満にするとオーステナイト安定度
を著しく不安定にする。また、2.0%を越えると
スケール性から鋼板表面性状に悪影響を与える。
このためMnの範囲を0.3〜2.0%とした。
Niはオーステナイト相を安定化する元素であ
り、その効果はMnの2倍である。8.0%を越える
とオーステナイト相が安定になり過ぎ、降伏比を
大きくし、加工性を劣化させる。6.0%未満では
オーステナイト相が不安定になり過ぎ、延性が劣
化する。従つてNiの範囲を6.0〜8.0%とした。
Crは耐食性およびフエライト形成には大きな
効果を有する。16.0%未満では耐食性が劣化し、
20%を越えるとフエライト量が増加し熱間加工性
が劣化する。このためCrの範囲を16.0〜20.0%に
限定した。なお、Crは加工誘起マルテンサイト
の生成を抑制する元素であるといわれているが20
%以下ではその影響が小さい。
このような成分のオーステナイト系ステンレス
鋼を固溶化熱処理し、900℃〜500℃の間を10℃/s
ec以上100℃/sec以下の平均冷却速度で冷却す
る。固溶化熱処理温度から冷却する際、900℃〜
500℃の間の平均冷却速度が10℃/secより遅いと
製品の粒界腐食感受性が敏感となる。また、この
間を100℃/secを越える平均冷却速度で冷却する
ことは実用上有益ではない。
次いで、調質圧延時の圧下率の限定理由につい
て述べる。第4図は0.06C−0.6Si−1.3Mn−7.3Ni
−17.3Cr−0.08N鋼について、試験圧延機により
調質圧延を行い、0.2%耐力と圧下率の関係を調
べたものである。第4図に示すように圧下率を増
すと0.2%耐力は増加し、圧下率が約5、10、20
%の時に0.2%耐力が50、60、80Kg/Hzになる。本
発明の成分範囲ではSi、Mn、Ni、Crを変化させ
ても目標の強度を得る圧下率はほとんど変化しな
い。しかし、C、Nが増すと同一圧下率での0.2
%耐力は増加し、目標の強度を得る圧下率は減少
する。この傾向は高強度側で顕著になる。このた
め調質圧延時の圧下率の範囲を50Kg/mm2級では3
〜7%、60Kg/mm2級では7〜13%、80Kg/mm2級で
は18〜26%とした。また、ロールギヤツプでの温
度を30〜50℃に限定したのは、30℃未満の低温に
なると圧下率の変動に対する0.2%耐力の変動が
大きくなり、調質圧延後の材質のバラツキを大き
くするからである。又、50℃を越えると加工誘起
マルテンサイトの生成が少くなり高強度が得にく
くなる。
以下に実施例をあげて本発明を説明する。表1
は実機設備にて製造試験を行つた結果である。本
発明成分に比較しNi、Crが高い鋼は伸びが低
く、降伏比が高い。このため加工性が劣る。また
Cを高め、Nを低めた材料は本発明鋼(本発明に
より製造した鋼)とほぼ同等の伸び、降伏比を有
するが、固溶化熱処理後の冷却速度が15℃/secで
は混合組織となつており本発明成分に比べ耐食性
が劣る。又、冷却速度が遅くなる厚手材において
は溶接部の粒界腐食は避けられず、溶接部の耐食
性、強度特性が劣化する。
以上実施例に見られるように、本発明鋼は加工
性および耐食性に優れ、特に、60Kg/mm2級以下の
クラスは加工性に優れており、複雑な形状に加工
する事が可能である。また80Kg/mm2級の鋼でも単
純な加工については問題ない。このような高強
度、高加工性、高耐食性を有する材料を用いれ
ば、車輛等の輸送機関の軽量化を容易に行う事が
でき、省エネルギー時代の到来を考えた場合その
利点は多大である。[Table] First, the influence of general components on mechanical properties is shown, and then the reasons for limiting each component are explained.
Figure 1 shows the influence of components on strength.
1.1~0.8mm by known cold rolling and annealing from 45Kg steel ingot
The measurements were taken on a material that was made into a thick steel plate and then temper-rolled in a temper rolling mill to a thickness of 0.8 mm.
As shown in the figure, C increases yield strength by 0.2% and decreases tensile strength on the low strength side. However, on the high strength side, the lower the C, the lower the tensile strength, and the C is 0.04%
This is particularly noticeable below. N is 0.2% like C
Increase yield strength and decrease tensile strength. The effect is greater than C. Ni shows no effect on 0.2% proof stress, but significantly reduces tensile strength. Cr and Mn show the same tendency as Ni, but their effectiveness is half that of Ni. Figure 2 comprehensively summarizes the influence of components on elongation at break. The manufacturing process is the same as in Figure 1, with C0.02~0.15%, Mn1~
2%, 6-9% Ni, 15-18% Cr, and 0.02-0.2% N. 1/ as shown in the figure
2Mn+Ni−1/12(20−Cr) 2 +15(C+N)(%)
As the value increases, the elongation increases. As described above, each component increases elongation, and alloying elements other than C and N significantly decrease tensile strength. As a result, the yield ratio increases. In order to obtain the best balance between strength and ductility, it is important to sufficiently control the proportions of C, N, and other alloying elements. The reasons for limiting the various components will be explained based on the above facts. While C stabilizes the austenite phase and suppresses the formation of a deformation-induced martensite phase, it also functions to solid-solution strengthen the austenite phase and the formed martensite phase, and the larger the amount, the more advantageous it is in terms of strength. When the C content is less than 0.04%, high strength cannot be obtained unless an excessive amount of martensitic phase is generated, resulting in deterioration of ductility. On the other hand, the upper limit of the amount of C was regulated based on susceptibility to intergranular corrosion. That is, FIG. 3 shows the results of a 10% oxalic acid electrolytic etch test performed on materials with different amounts of C while changing the cooling rate between 900°C and 500°C. As shown in the same figure, it can be seen that when C exceeds 0.07%, susceptibility to intergranular corrosion becomes sensitive. Therefore, the range of C was set to 0.04% to 0.07%. N has the same function as C, and a larger amount is advantageous in terms of strength, but if it exceeds 0.15%, it causes blowholes, and if it is less than 0.05%, the austenite phase becomes too unstable. For this reason, the range of N is
It was set at 0.05-0.15%. Si is necessary for steelmaking as a deoxidizing agent, but 1.0%
If it exceeds 1.0%, the ferrite forming ability becomes strong and hot workability deteriorates, so the upper limit was set at 1.0%. Mn is an element that stabilizes the austenite phase, and when it is less than 0.3%, the austenite stability becomes extremely unstable. Moreover, if it exceeds 2.0%, it will adversely affect the surface properties of the steel sheet due to scaling.
Therefore, the Mn content was set in the range of 0.3 to 2.0%. Ni is an element that stabilizes the austenite phase, and its effect is twice that of Mn. If it exceeds 8.0%, the austenite phase becomes too stable, increasing the yield ratio and deteriorating workability. If it is less than 6.0%, the austenite phase becomes too unstable and ductility deteriorates. Therefore, the range of Ni was set to 6.0 to 8.0%. Cr has a great effect on corrosion resistance and ferrite formation. If it is less than 16.0%, corrosion resistance will deteriorate;
If it exceeds 20%, the amount of ferrite increases and hot workability deteriorates. For this reason, the range of Cr was limited to 16.0% to 20.0%. Note that Cr is said to be an element that suppresses the formation of deformation-induced martensite20.
% or less, the effect is small. Austenitic stainless steel with these components is solution heat treated and heated at 10℃/s between 900℃ and 500℃.
Cool at an average cooling rate of ec or more and 100°C/sec or less. When cooling from the solution heat treatment temperature, 900℃~
If the average cooling rate during 500℃ is slower than 10℃/sec, the product becomes sensitive to intergranular corrosion. Moreover, cooling at an average cooling rate exceeding 100° C./sec during this period is not practically useful. Next, the reason for limiting the rolling reduction during temper rolling will be described. Figure 4 shows 0.06C−0.6Si−1.3Mn−7.3Ni
-17.3Cr-0.08N steel was subjected to temper rolling using a test rolling mill, and the relationship between 0.2% proof stress and rolling reduction was investigated. As shown in Figure 4, as the rolling reduction rate increases, the 0.2% yield strength increases, and as the rolling reduction rate increases to approximately 5, 10, and 20
%, the 0.2% yield strength becomes 50, 60, 80Kg/Hz. In the composition range of the present invention, even if Si, Mn, Ni, and Cr are changed, the rolling reduction ratio to obtain the target strength hardly changes. However, when C and N increase, 0.2
The % yield strength increases and the reduction rate to obtain the target strength decreases. This tendency becomes more noticeable on the high strength side. For this reason, the range of rolling reduction during temper rolling is 50Kg/mm and 3 for grade 2 .
-7%, 7-13% for 60Kg/mm 2nd grade, and 18-26% for 80Kg/mm 2nd grade. In addition, the temperature at the roll gap was limited to 30 to 50°C because if the temperature is lower than 30°C, the fluctuation of the 0.2% yield strength in response to changes in rolling reduction will increase, which will increase the variation in material quality after temper rolling. It is. Moreover, when the temperature exceeds 50°C, the formation of deformation-induced martensite decreases, making it difficult to obtain high strength. The present invention will be explained below with reference to Examples. Table 1
These are the results of manufacturing tests conducted using actual equipment. Steels with higher Ni and Cr content than those of the present invention have lower elongation and higher yield ratio. For this reason, workability is poor. In addition, materials with high C and low N have elongation and yield ratio that are almost the same as the steel of the present invention (steel produced according to the present invention), but when the cooling rate after solution heat treatment is 15°C/sec, the material has a mixed structure. The corrosion resistance is inferior to the components of the present invention. In addition, in thick materials where the cooling rate is slow, intergranular corrosion of the weld is unavoidable, resulting in deterioration of the corrosion resistance and strength characteristics of the weld. As can be seen in the examples above, the steel of the present invention has excellent workability and corrosion resistance, and in particular, steel of the 60 kg/mm 2 class or lower class has excellent workability and can be processed into complex shapes. Also, there is no problem with simple processing even with 80Kg/mm 2nd class steel. By using materials with such high strength, high workability, and high corrosion resistance, it is possible to easily reduce the weight of transportation systems such as vehicles, and this has many advantages when considering the arrival of an energy-saving era.
【表】【table】
第1図は強度に対する成分の影響を示す図、第
2図は破断伸びに対する成分の影響を示した図、
第3図は17Cr−7Ni系を基本組成としてCを変化
させた材料について、固溶化処理後900℃から500
℃の間の冷却速度を変化させて冷却した後、10%
蓚酸電解エツチテストを行つた結果を示す図(図
中の○は段状組織、●は混合組織又はみぞ状組織
を意味する。)、第4図は0.06C−0.6Si−1.3Mn−
7.3Ni−17.3Cr−0.08N鋼について、実験室的に調
質圧延を行い、0.2%耐力と調質圧延時の圧下率
との関係を示す図である。
Figure 1 is a diagram showing the influence of components on strength, Figure 2 is a diagram showing the influence of components on elongation at break,
Figure 3 shows materials with a basic composition of 17Cr-7Ni and varying C.
After cooling by varying the cooling rate between ℃10%
A figure showing the results of an oxalic acid electrolytic etch test (○ in the figure means a step-like structure, ● means a mixed structure or a groove-like structure), Figure 4 is 0.06C−0.6Si−1.3Mn−
7.3Ni-17.3Cr-0.08N steel is subjected to temper rolling in a laboratory and is a diagram showing the relationship between 0.2% yield strength and rolling reduction during temper rolling.
Claims (1)
0.15%、Si;1.0以下、Mn;0.3〜2.0%、Ni;6.0
〜8.0%、Cr;16.0〜20.0%を含有し、残部はFe
および製鋼上不可避の元素からなるオーステナイ
ト系ステンレス鋼を固溶化熱処理し、900〜500℃
の間を10℃/sec以上100℃/sec以下の平均冷却速
度で冷却し、次いでロールギヤツプにおける材料
温度を30〜50℃に保持し、製品に要求される強度
に応じて下記条件による冷間調質圧延を行うこと
を特徴とする高強度ステンレス鋼板の製造方法。 【表】[Claims] 1. C: 0.04-0.07%, N: 0.05-0.05% by weight
0.15%, Si; 1.0 or less, Mn; 0.3-2.0%, Ni; 6.0
~8.0%, Cr; Contains 16.0~20.0%, the balance is Fe
and austenitic stainless steel, which consists of elements unavoidable in steel manufacturing, are solution heat treated at 900 to 500℃.
The material temperature in the roll gap is maintained at 30 to 50°C, and cold conditioning is performed under the following conditions depending on the strength required for the product. A method for manufacturing a high-strength stainless steel sheet, characterized by performing quality rolling. 【table】
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP55181336A JPS57104628A (en) | 1980-12-23 | 1980-12-23 | Production of high-strength stainless steel plate |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP55181336A JPS57104628A (en) | 1980-12-23 | 1980-12-23 | Production of high-strength stainless steel plate |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS57104628A JPS57104628A (en) | 1982-06-29 |
| JPS6119687B2 true JPS6119687B2 (en) | 1986-05-19 |
Family
ID=16098908
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP55181336A Granted JPS57104628A (en) | 1980-12-23 | 1980-12-23 | Production of high-strength stainless steel plate |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS57104628A (en) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6026619A (en) * | 1983-07-22 | 1985-02-09 | Nippon Kokan Kk <Nkk> | Manufacture of austenitic stainless steel plate |
| FR2777811B1 (en) * | 1998-04-23 | 2000-05-19 | Usinor | AUSTENITIC STAINLESS STEEL SHEET USED IN THE FIELD OF THE CELLAR AND IN PARTICULAR IN THE FIELD OF THE WINE CELLAR |
| DE19940795A1 (en) * | 1999-08-27 | 2001-03-01 | Lohmann Therapie Syst Lts | Rapidly disintegrating pellets based on chitosan |
| CN102601282B (en) * | 2012-03-08 | 2013-12-25 | 无锡市法兰锻造有限公司 | Z2CND18-12N control nitrogen stainless steel forging technology |
| CN103266286A (en) * | 2013-06-14 | 2013-08-28 | 兰州理工大学 | High-alumina 316L stainless steel and preparation method thereof |
-
1980
- 1980-12-23 JP JP55181336A patent/JPS57104628A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS57104628A (en) | 1982-06-29 |
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