JP2565038B2 - Method for producing high-strength galvannealed steel sheet with excellent strength-ductility balance and film properties - Google Patents
Method for producing high-strength galvannealed steel sheet with excellent strength-ductility balance and film propertiesInfo
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- JP2565038B2 JP2565038B2 JP3295186A JP29518691A JP2565038B2 JP 2565038 B2 JP2565038 B2 JP 2565038B2 JP 3295186 A JP3295186 A JP 3295186A JP 29518691 A JP29518691 A JP 29518691A JP 2565038 B2 JP2565038 B2 JP 2565038B2
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Description
【0001】[0001]
【産業上の利用分野】本発明は、主に自動車用素材とし
て用いられる高強度溶融亜鉛めっき鋼板の製造方法に係
り、特に引張強度が50〜70kg/mm2で強度−延
性バランスに優れ、しかも優れた皮膜特性を兼ね備えた
合金化溶融亜鉛めっき鋼板の製造方法に関するものであ
る。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a method for producing a high-strength hot-dip galvanized steel sheet which is mainly used as a material for automobiles, and particularly has a tensile strength of 50 to 70 kg / mm 2 and an excellent strength-ductility balance. The present invention relates to a method for producing an alloyed hot-dip galvanized steel sheet having excellent film properties.
【0002】[0002]
【従来の技術】近年、地球温暖化防止等の観点から自動
車の燃費向上が叫ばれ、車体軽量化と安全性確保の観点
から素材の高強度・薄物化が強く求められている。一
方、車体寿命延長の観点から、合金化溶融亜鉛めっき鋼
板が車体用素材として使用され始めて久しい。したがっ
て、これら両特性を満足させるために高強度合金化溶融
亜鉛めっき鋼板の開発が行われている。2. Description of the Related Art In recent years, improvement in fuel efficiency of automobiles has been called for from the viewpoint of prevention of global warming and the like, and high strength and thin materials are strongly demanded from the viewpoint of weight reduction of a vehicle body and ensuring safety. On the other hand, alloyed hot-dip galvanized steel sheets have long been used as body materials from the viewpoint of extending the life of the vehicle body. Therefore, development of high-strength hot-dip galvanized steel sheets has been carried out in order to satisfy both of these characteristics.
【0003】一般的に、鋼板の強度上昇にはSi,M
n,P等の固溶強化型元素の添加、Nb,Ti,V等の
析出型元素の添加、あるいはそれら両者の複合添加等が
行われている。ところが、引張強度を50kg/mm2
以上とするためには、前者のみでは各強化元素の添加量
を多くする必要があり、特にこれらの強化元素は連続溶
融亜鉛めっきライン(以下、CGLという)での焼鈍時
に鋼板表面に濃化し、皮膜特性を低下(不めっき、合金
化不良、耐パウダリング性不良等)させるという難点が
ある。一方、後者では、鋼中に多量の析出物が存在する
ため、再結晶温度が上昇し、さらに強度−延性バランス
や穴拡げ性が劣る等、材質上の難点がある。Generally, Si and M are used to increase the strength of steel sheets.
The addition of solid solution strengthening elements such as n and P, the addition of precipitation elements such as Nb, Ti and V, or the combined addition of both of these is performed. However, the tensile strength was 50 kg / mm 2
To achieve the above, it is necessary to increase the amount of addition of each strengthening element only with the former, and these strengthening elements are concentrated on the steel plate surface during annealing in a continuous hot-dip galvanizing line (hereinafter referred to as CGL), There is a problem that the film characteristics are deteriorated (non-plating, poor alloying, poor powdering resistance, etc.). On the other hand, in the latter case, since a large amount of precipitates are present in the steel, the recrystallization temperature rises, and further, the strength-ductility balance and the hole expandability are inferior, which is a material problem.
【0004】上記強化機構とは別に、マルテンサイト等
の硬質第2相を軟質フェライト中に分散させる複合組織
化によって鋼を強化することが知られている。この方法
では、強度−延性バランスに優れ、その上、降伏比が低
下するために形状凍結性が改善される等、プレス成形性
も向上する。Apart from the above strengthening mechanism, it is known to strengthen steel by a composite structure in which a hard second phase such as martensite is dispersed in soft ferrite. According to this method, the balance between strength and ductility is excellent, and in addition, since the yield ratio is lowered, the shape fixability is improved, and the press formability is also improved.
【0005】[0005]
【発明が解決しようとする課題】一般に、このような複
合組織化は鋼板をAc1変態点以上、Ac3変態点以下の温
度領域に加熱後冷却し、オーステナイトをマルテンサイ
ト等の硬質低温変態相に変態させることによって達成さ
れる。このような低温変態相の形成には、冷却途中で如
何にオーステナイト相を安定化させるか、換言すればオ
ーステナイトからパーライトへの変態を抑制するかが重
要である。すなわち、CGLのように焼鈍後の冷却速度
が比較的遅く、しかも冷却途中に450℃〜500℃で
のめっき工程および450〜550℃での合金化処理工
程が存在する場合には、オーステナイト相を安定化させ
るためにMn,Si,Cr等を多量に添加する必要があ
り、上述した固溶強化型と同様の問題を生じる。Generally, in such a composite structure, a steel sheet is heated to a temperature range of Ac 1 transformation point or more and Ac 3 transformation point or less and then cooled, and austenite is transformed into a hard low temperature transformation phase such as martensite. It is achieved by transforming into. To form such a low temperature transformation phase, it is important how to stabilize the austenite phase during cooling, in other words, to suppress transformation from austenite to pearlite. That is, when the cooling rate after annealing is relatively slow like CGL, and the plating step at 450 ° C. to 500 ° C. and the alloying treatment step at 450 ° C. to 550 ° C. are present during cooling, an austenite phase is formed. In order to stabilize it, it is necessary to add a large amount of Mn, Si, Cr or the like, which causes the same problem as the solid solution strengthening type described above.
【0006】例えば、特公昭58−30933号は複合
組織型合金化溶融亜鉛めっき鋼板の製造方法に関するも
のであるが、オーステナイトを安定化させるためにMn
+Si≧2.3とし、さらに、めっき浴と合金化炉との
間に保持帯という特殊な帯域を設けなければならない。For example, Japanese Examined Patent Publication No. 58-30933 relates to a method for producing a composite structure type alloyed hot-dip galvanized steel sheet, and in order to stabilize austenite, Mn is used.
+ Si ≧ 2.3, and a special zone called a retention zone must be provided between the plating bath and the alloying furnace.
【0007】一方、通常の溶融亜鉛めっき鋼板(非合金
化材)についても、特公昭62−13415号や特開昭
54−148125号等の技術が開示されている。これ
らの技術では、成分系としてSi:tr.材を使用する
が、Mn:1.5wt%以下、Cr:0.5wt%以下
であり、このような鋼種を合金化処理すると、Mn,C
rの表面濃化に起因する合金化ムラ(合金化異常)が発
生し、皮膜品質が劣化してしまう。さらに、CGLでの
冷却途中に加熱工程(合金化加熱処理)が加わるため
に、強度低下も避けられない。On the other hand, with respect to ordinary hot-dip galvanized steel sheets (non-alloyed materials), techniques such as Japanese Patent Publication No. 62-13415 and Japanese Unexamined Patent Publication No. 54-148125 are disclosed. In these techniques, Si: tr. The material is Mn: 1.5 wt% or less and Cr: 0.5 wt% or less. When alloying such a steel type, Mn, C
The alloying unevenness (alloying abnormality) occurs due to the surface concentration of r, and the film quality deteriorates. Furthermore, since a heating step (alloying heat treatment) is added during the cooling in CGL, strength reduction cannot be avoided.
【0008】このように従来では、強度−延性バランス
の優れた引張強度50kg/mm2以上の高強度合金化
溶融亜鉛めっき鋼板を製造するためには、皮膜特性(め
っき性、合金化処理性)に有害な成分元素を多量に添加
したり、さらには特殊な製造設備を使用せざるを得ない
という問題があった。As described above, conventionally, in order to produce a high-strength galvannealed steel sheet having a tensile strength of 50 kg / mm 2 or more, which has an excellent strength-ductility balance, coating characteristics (plating property, alloying processability) are required. However, there is a problem in that a large amount of harmful component elements are added and that a special manufacturing facility must be used.
【0009】[0009]
【課題を解決するための手段】本発明はこのような従来
法の問題に鑑み、合金化溶融亜鉛めっき鋼板に要求され
る種々の特性を考慮しつつ、強度−延性バランスの優れ
た引張強度レベル50〜70kg/mm2を現出させる
強化機構を見直し、さらに、合金化処理時の加熱を誘導
加熱方式で行うことにより、原板表層の局所加熱を利用
してCGL焼鈍後冷却途中でのオーステナイトのパーラ
イトへの変態を極力抑えるとともに、耐パウダリング
性、合金相の均質性にも優れた皮膜が得られるようにし
たものである。In view of the problems of the conventional method, the present invention considers various properties required for the galvannealed steel sheet, and has a tensile strength level excellent in strength-ductility balance. By reviewing the strengthening mechanism that makes 50 to 70 kg / mm 2 appear, and by performing heating during alloying by an induction heating method, local heating of the original plate surface layer is used to utilize austenite during cooling after CGL annealing. In addition to suppressing the transformation into pearlite as much as possible, a film having excellent powdering resistance and alloy phase homogeneity can be obtained.
【0010】すなわち本発明は、C:0.08〜0.1
4wt%、Si:0.15〜0.35wt%、Mn:
1.50〜2.00wt%、P:0.05wt%以下、
S:0.02wt%以下、Sol.Al:0.03〜
0.06wt%、N:0.0070wt%以下、Cr:
0.15〜0.25wt%、V:0.050〜0.10
0wt%を含有し、残部Feおよび不可避的不純物から
なる組成を有する鋼を、熱延スラブ加熱温度:1170
℃以下、熱延巻取温度:600℃以下の条件で熱間圧延
し、必要に応じて冷間圧延した後、連続溶融亜鉛めっき
ラインにおいて、Ac1変態点以上、Ac3変態点以下の温
度で焼鈍した後めっきし、次いで、誘導加熱方式の合金
化炉において炉出側板温が450〜550℃となるよう
合金化加熱処理を行い、表層の溶融亜鉛層が消滅後、3
00℃以下の温度までを10℃/sec以上の冷却速度
で冷却することを特徴とする強度−延性バランスおよび
皮膜特性に優れた高強度合金化溶融亜鉛めっき鋼板の製
造方法である。That is, in the present invention, C: 0.08 to 0.1
4 wt%, Si: 0.15 to 0.35 wt%, Mn:
1.50 to 2.00 wt%, P: 0.05 wt% or less,
S: 0.02 wt% or less, Sol. Al: 0.03 ~
0.06 wt%, N: 0.0070 wt% or less, Cr:
0.15-0.25 wt%, V: 0.050-0.10.
A steel containing 0 wt% and having a composition of balance Fe and unavoidable impurities was formed into a hot rolled slab at a heating temperature of 1170.
℃ or less, hot rolling winding temperature: after hot rolling under the conditions of 600 ℃ or less, and cold rolling if necessary, in the continuous hot dip galvanizing line, a temperature of Ac 1 transformation point or more and Ac 3 transformation point or less After annealing, the alloy is subjected to alloying heat treatment in an induction heating type alloying furnace so that the furnace exit side plate temperature is 450 to 550 ° C., and after the molten zinc layer on the surface layer disappears, 3
A method for producing a high-strength galvannealed steel sheet having excellent strength-ductility balance and coating properties, which is characterized by cooling to a temperature of 00 ° C or lower at a cooling rate of 10 ° C / sec or higher.
【0011】このような本発明の特徴は、材質的にはS
i−Mn−Cr系による複合組織化とV添加による組織
の細粒化との組み合わせにより、低成分系でありながら
優れた強度−延性バランスを付与したこと、合金化加熱
処理に誘導加熱方式を用いることにより、CGL加熱後
の合金化処理工程を含めた冷却過程における鋼板の再加
熱を極力抑え、低成分系でありながらオーステナイトか
らパーライトへの変態を抑制したこと、さらには、皮膜
特性の観点から、熱延条件を適正化することにより、ス
ラブ加熱工程を含む熱延工程において形成されるめっき
原板表面の不均一性(これらの不均一性は、CGLにお
ける合金化処理時に局部的な合金化ムラを引き起こす)
を抑制し、さらに、CGLの加熱工程で生じるSi,M
n,Cr等、易酸化性元素の選択酸化物による合金化異
常を誘導加熱方式の合金化処理により無害化する(めっ
き原板の表層が優先的に加熱されるため、合金化阻害物
の影響を受けにくい)ことにある。そして、このような
本発明によれば、設備の改造等を行うことなく、強度−
延性バランスおよびめっき性、特に表面外観、耐パウダ
リング性の優れた50〜70kg/mm2級高強度合金
化溶融亜鉛めっき鋼板を製造することが可能である。Such a feature of the present invention is S in terms of material.
The combination of i-Mn-Cr-based composite structure and V-added structure for fine-grained structure imparted an excellent strength-ductility balance in spite of being a low component system, and the induction heating method was used for the alloying heat treatment. By using it, the reheating of the steel sheet in the cooling process including the alloying treatment step after CGL heating was suppressed as much as possible, and the transformation from austenite to pearlite was suppressed even though it was a low component system. Therefore, by optimizing the hot rolling conditions, the non-uniformity of the surface of the plating base plate formed in the hot rolling process including the slab heating process (these non-uniformities are caused by local alloying during the alloying process in CGL). Cause unevenness)
Is suppressed, and Si and M generated in the heating process of CGL are suppressed.
Anomalous alloying caused by selective oxides of easily oxidizable elements such as n, Cr, etc. is rendered harmless by induction heating alloying treatment (because the surface layer of the plating original plate is preferentially heated, the influence of alloying inhibitors is Hard to receive). Further, according to the present invention as described above, the strength-
It is possible to produce a 50-70 kg / mm 2 grade high strength alloyed galvanized steel sheet having excellent ductility balance and plating properties, particularly surface appearance and powdering resistance.
【0012】[0012]
【作用】まず、本発明法におけるめっき原板の成分組成
の限定理由について説明する。 C:複合組織鋼板においては、C量は焼鈍温度とともに
第2相体積率を決定する重要な要素である。Cが0.0
8wt%未満では第2相体積率が不十分であり、引張強
度50kg/mm2以上を得るためには固溶強化或いは
析出強化元素を多量に添加する必要があり、強度−延性
バランスおよびめっき性の低下をもたらす。一方、Cが
0.14wt%を超えると第2相体積率が増加し、延性
が低下するとともに、スポット溶接性も低下する。この
ためCは0.08〜0.14wt%と規定する。First, the reasons for limiting the component composition of the original plating plate in the method of the present invention will be described. C: In a steel sheet having a composite structure, the amount of C is an important factor that determines the second phase volume ratio together with the annealing temperature. C is 0.0
If it is less than 8 wt%, the volume fraction of the second phase is insufficient, and in order to obtain a tensile strength of 50 kg / mm 2 or more, it is necessary to add a large amount of solid solution strengthening or precipitation strengthening elements. Bring about a decline. On the other hand, when C exceeds 0.14 wt%, the second phase volume ratio increases, the ductility decreases, and the spot weldability also decreases. Therefore, C is defined as 0.08 to 0.14 wt%.
【0013】Si:Siはフェライト中の固溶Cを減少
させ、オーステナイトを安定化させるとともに、延性を
劣化させずにフェライトを強化する元素であるが、めっ
き性および合金化処理性に対して悪影響を及ぼすことが
知られている。しかしながら、後述するような製造条件
の最適化(熱延スラブ加熱温度、熱延巻取温度および誘
導加熱方式合金化炉の採用等)により、少量ならば添加
できることが判明した。Si添加は強度−延性バランス
改善という本発明の特徴の1つである。Siが0.15
wt%未満では、上述したような延性改善効果が得られ
ない。一方、0.35wt%を超えると、上記製造条件
の最適化を行っても合金化処理性への影響が現れ、表面
外観が劣化するようになる。このためSiは0.15〜
0.35wt%と規定する。Si: Si is an element that reduces the solid solution C in the ferrite, stabilizes austenite, and strengthens the ferrite without deteriorating the ductility, but has an adverse effect on the plating property and alloying processability. Is known to affect. However, by optimizing the production conditions as described later (hot rolling slab heating temperature, hot rolling coiling temperature, induction heating type alloying furnace, etc.), it was found that a small amount can be added. The addition of Si is one of the features of the present invention that the strength-ductility balance is improved. Si is 0.15
If it is less than wt%, the above-mentioned effect of improving ductility cannot be obtained. On the other hand, if it exceeds 0.35 wt%, the alloying processability is affected even if the above manufacturing conditions are optimized, and the surface appearance is deteriorated. Therefore, Si is 0.15
It is specified as 0.35 wt%.
【0014】Mn:Mnはオーステナイトを安定化さ
せ、CGL冷却過程でのパーライトへの変態を抑制する
とともに、フェライト中に固溶し鋼を強化する。Mnが
1.50wt%未満ではこのような効果が十分得られ
ず、一方、2.00wt%を超えるとSiとともにCG
L加熱時に鋼板表面に濃化し、合金化処理性への影響が
現れる。このためMnは1.50〜2.00wt%と規
定する。Mn: Mn stabilizes austenite, suppresses transformation to pearlite in the CGL cooling process, and strengthens steel by forming a solid solution in ferrite. If Mn is less than 1.50 wt%, such an effect cannot be sufficiently obtained, while if Mn exceeds 2.00 wt%, CG is added together with Si.
When L is heated, it concentrates on the surface of the steel sheet and the alloying processability is affected. Therefore, Mn is defined as 1.50 to 2.00 wt%.
【0015】P:Pは延性を害さずに鋼を強化する固溶
強化元素の1つであるが、過度の添加は合金化処理性に
影響を与え、合金化ムラを生じる原因となる。このため
Pは0.05wt%を上限として添加される。 S:Sが0.02wt%を超えると熱間圧延時に割れが
発生し易くなるとともに、冷間での延性を劣化させるた
め、0.02wt%をその上限とする。P: P is one of the solid solution strengthening elements that strengthens steel without impairing ductility, but excessive addition affects alloying processability and causes uneven alloying. Therefore, P is added with an upper limit of 0.05 wt%. S: If S exceeds 0.02 wt%, cracks are likely to occur during hot rolling and ductility in cold is deteriorated, so 0.02 wt% is the upper limit.
【0016】Sol.Al:Alは製鋼時の脱酸剤とし
て添加されるが、過度に添加すると選択酸化によってめ
っき性に悪影響を及ぼす。AlはSol.Alで0.0
3wt%未満では脱酸効果が十分でなく、一方、0.0
6wt%を超えると上述した選択酸化によってめっき性
が劣化する。このためSol.Alは0.03〜0.0
6wt%と規定する。 N:Nは多量に含まれると延性を劣化させるため、0.
0070wt%をその上限とする。Sol. Al: Al is added as a deoxidizing agent during steel making, but if added excessively, it has a bad influence on the plating property due to selective oxidation. Al is Sol. 0.0 for Al
If it is less than 3 wt%, the deoxidizing effect is insufficient, while 0.0
If it exceeds 6 wt%, the above-mentioned selective oxidation deteriorates the plating property. Therefore, Sol. Al is 0.03 to 0.0
It is specified as 6 wt%. N: N, if contained in a large amount, deteriorates ductility.
The upper limit is 0070 wt%.
【0017】Cr:Crは0.15wt%以上の添加で
オーステナイトの安定性を高めるが、過度に添加すると
選択酸化によってめっき性に悪影響を及ぼす。このため
Crは0.15〜0.25wt%と規定する。 V:Vは炭窒化物として鋼中に析出することにより、2
相域加熱時にフェライトおよびオーステナイトの結晶粒
径を効果的に微細化する。このような効果は0.050
wt%未満では得ることができず、一方、0.100w
t%を超えると析出物の量が多くなるため再結晶温度が
上昇してしまう。このためVは0.050〜0.100
wt%と規定する。Cr: Cr increases the stability of austenite when added in an amount of 0.15 wt% or more, but excessive addition adversely affects the plating property due to selective oxidation. Therefore, Cr is defined as 0.15 to 0.25 wt%. V: V is deposited as carbonitride in the steel, resulting in 2
Effectively refines the crystal grain size of ferrite and austenite during heating in the phase region. Such effect is 0.050
If it is less than wt%, it cannot be obtained, while 0.100w
If it exceeds t%, the amount of precipitates increases and the recrystallization temperature rises. Therefore, V is 0.050 to 0.100.
Defined as wt%.
【0018】以上のような成分組成の鋼スラブは、熱延
スラブ加熱温度:1170℃以下、熱延巻取温度:60
0℃以下の条件で熱間圧延される。熱延スラブ加熱温度
は熱延巻取温度とともに本発明の重要な製造条件の1つ
である。鋼中にSiを添加するとMnを多量に添加しな
くてもオーステナイトが安定化し、さらに強度−延性バ
ランスが改善される。しかしながら、Siの添加は合金
化処理性に悪影響を及ぼすことは前述した通りである。
本発明者らはこれらについて詳細な検討を行った結果、
Si鋼の合金化異常は以下に述べる2種類の現象からな
ることが明らかとなった。その1つは、図1の写真に示
すような合金化反応の不均一性であり、また他の1つは
図2の写真に示すようなフェライト結晶粒界での選択的
なFe−Zn反応による合金化異常である。これらにつ
いて熱延条件の影響を調査した結果、図3に示すよう
に、前者のタイプの合金化異常(図中、「タイプ」と
して示す)は熱延スラブ加熱温度により、また後者のタ
イプの合金化異常(図中、「タイプ」として示す)は
熱延巻取温度によって出現傾向が変化することが判明し
た。これらの理由は必ずしも明らかではないが、前者は
熱延スラブ加熱時に形成される鉄・Siの複合酸化物の
形成と、また後者は熱延巻取中に起こる表面フェライト
結晶粒界部でのSiの選択酸化現象が関与しているもの
と思われる。図3によれば、熱延スラブ加熱温度117
0℃以下、熱延巻取温度600℃以下の条件で熱延を行
えば、上述したいずれのタイプの合金化異常も生じてい
ない。以上のような結果から、本発明では熱延スラブ加
熱温度を1170℃以下、熱延巻取温度を600℃以下
と規定した。The steel slab having the above-described composition is a hot rolling slab heating temperature: 1170 ° C. or lower, a hot rolling coiling temperature: 60.
It is hot-rolled under the condition of 0 ° C or less. The hot rolling slab heating temperature is one of the important manufacturing conditions of the present invention together with the hot rolling coiling temperature. When Si is added to steel, austenite is stabilized without adding a large amount of Mn, and the strength-ductility balance is further improved. However, as described above, the addition of Si adversely affects the alloying processability.
As a result of detailed investigations by the present inventors,
It became clear that the alloying abnormality of Si steel consists of the following two types of phenomena. One is the non-uniformity of the alloying reaction as shown in the photograph of Fig. 1, and the other is the selective Fe-Zn reaction at the ferrite grain boundaries as shown in the photograph of Fig. 2. It is an abnormal alloying. As a result of investigating the influence of hot rolling conditions on these, as shown in FIG. 3, the alloying anomaly of the former type (indicated as “type” in the figure) is caused by the hot rolling slab heating temperature and the alloy of the latter type. It has been found that the abnormal appearance (shown as "type" in the figure) changes its appearance tendency depending on the hot rolling coiling temperature. Although the reasons for these are not clear, the former is the formation of a composite oxide of iron and Si formed during heating of the hot rolling slab, and the latter is the Si at the grain boundary of the surface ferrite that occurs during hot rolling. It seems that the selective oxidation phenomenon of is involved. According to FIG. 3, the hot rolling slab heating temperature 117
When hot rolling is performed under the conditions of 0 ° C. or lower and the hot rolling coiling temperature of 600 ° C. or lower, neither of the above-mentioned types of alloying abnormality occurs. From the above results, in the present invention, the hot rolling slab heating temperature is defined as 1170 ° C. or lower and the hot rolling coiling temperature is defined as 600 ° C. or lower.
【0019】上記熱延後の鋼板は、酸洗後必要に応じて
冷間圧延された後、CGLに通板される。このCGLに
おける焼鈍加熱温度はAc1変態点以上、Ac3変態点以下
の2相温度域とする。この2相温度域での焼鈍では、そ
の焼鈍温度に応じて2相体積率が変化し、したがって、
焼鈍温度によって強度レベルを任意に変化させることが
できる。焼鈍後の鋼板は常法に従い直ちに冷却される。
本発明ではこの際の冷却速度は特に規定しないが、通常
のCGLで達成される冷却速度により本発明の成分系は
2相組織化する。The hot-rolled steel sheet is pickled, cold-rolled if necessary, and then passed through CGL. The annealing heating temperature in this CGL is in the two-phase temperature range from the Ac 1 transformation point to the Ac 3 transformation point. In the annealing in this two-phase temperature range, the two-phase volume ratio changes according to the annealing temperature, and therefore,
The strength level can be arbitrarily changed by the annealing temperature. The annealed steel sheet is immediately cooled according to the usual method.
In the present invention, the cooling rate at this time is not particularly specified, but the component system of the present invention has a two-phase structure due to the cooling rate achieved by ordinary CGL.
【0020】次いで鋼板は溶融めっきされ、付着量調整
後、合金化加熱処理がなされる。この合金化加熱処理は
誘導加熱(高周波誘導加熱)方式の合金化炉で実施され
る。このように合金化処理を誘導加熱方式の合金化炉で
行うことが本発明の特徴の1つであり、これによってS
i:0.15〜0.35wt%、Mn:1.50〜2.
00wt%のような添加元素範囲の鋼板でも、合金化異
常が抑制され、しかも2相域加熱後の冷却過程における
鋼板内質の再加熱を極力抑え、低成分系でありながらオ
ーステナイトからパーライトへの変態を抑制することが
できる。Next, the steel sheet is hot-dipped, and after the amount of adhesion is adjusted, an alloying heat treatment is performed. This alloying heat treatment is carried out in an induction heating (high frequency induction heating) type alloying furnace. It is one of the features of the present invention that the alloying treatment is performed in the induction heating type alloying furnace as described above.
i: 0.15 to 0.35 wt%, Mn: 1.50 to 2.
Even in steel sheets with an additive element range such as 00 wt%, alloying abnormalities are suppressed, and further reheating of the steel sheet contents during the cooling process after heating in the two-phase region is suppressed to the utmost. Metamorphosis can be suppressed.
【0021】上述したように、本発明の成分系の鋼を前
述した製造条件で熱延すれば、スラブ加熱を含む熱延工
程で生じる原板表面の不均一性に起因した合金化異常を
改善することができる。しかしながら、CGLの焼鈍時
にも添加元素の量に応じて選択酸化が起るため、めっき
浴浸漬直前の鋼板表面にはSi・Mn系等の複合酸化物
が島状に存在する。このような酸化物も合金化異常や著
しい場合には不めっきを引き起こすことが知られてい
る。合金化処理に誘導加熱方式の加熱炉を使用した場合
には、通常用いられるガス加熱方式と異なり鋼板表層が
優先的に加熱され、このような加熱によって鋼板表面の
不均一性に拘らず強制的に表層の鉄と溶融亜鉛との反応
が起こり、合金化異常が抑制されるものと考えられる。
さらに、このような加熱により効率的に合金化反応が起
こるため短時間で合金化が終了し、オーステナイトから
パーライトへの変態も抑制され、特に、上記のように鋼
板表層が優先的に加熱されるため、鋼板内部でのオース
テナイトからパーライトへの変態がより効果的に抑制さ
れる。As described above, when the steel of the composition system of the present invention is hot-rolled under the above-mentioned manufacturing conditions, the alloying anomaly caused by the nonuniformity of the surface of the original plate caused in the hot-rolling process including slab heating is improved. be able to. However, since the selective oxidation occurs according to the amount of the additional element even during the annealing of CGL, the complex oxide such as Si / Mn system exists in the form of islands on the surface of the steel sheet immediately before the immersion in the plating bath. It is known that such oxides also cause alloying abnormalities and, in extreme cases, non-plating. When an induction heating furnace is used for the alloying treatment, the surface layer of the steel sheet is preferentially heated, unlike the normally used gas heating method, and such heating forces the steel sheet surface to be non-uniform regardless of its non-uniformity. It is considered that the reaction between the surface iron and molten zinc occurs and the abnormal alloying is suppressed.
Furthermore, since the alloying reaction efficiently occurs due to such heating, alloying is completed in a short time, the transformation from austenite to pearlite is also suppressed, and in particular, the steel sheet surface layer is preferentially heated as described above. Therefore, the transformation from austenite to pearlite inside the steel sheet is more effectively suppressed.
【0022】以上のような合金化処理において、鋼板の
炉出側板温は450〜550℃の範囲に規定される。炉
出側板温が450℃未満では合金化に時間を要し、一
方、550℃を超えると耐パウダリング性が劣化する。
上記合金化処理において表層の溶融亜鉛層が消滅後、3
00℃以下の温度までを10℃/sec以上の冷却速度
で冷却する。耐パウダリング性改善には、特に合金化処
理後の過合金化の防止が重要であり、このためには合金
化加熱によって表層の溶融亜鉛層が消滅した後、合金化
が進行しない温度領域(300℃以下)までを10℃/
sec以上の冷却速度で冷却し、過合金化を防止する必
要がある。In the alloying treatment as described above, the temperature of the steel plate on the furnace outlet side is regulated within the range of 450 to 550 ° C. If the temperature at the furnace outlet side is less than 450 ° C, it takes a long time for alloying, while if it exceeds 550 ° C, the powdering resistance is deteriorated.
After the molten zinc layer on the surface layer disappeared in the above alloying treatment, 3
It is cooled to a temperature of 00 ° C. or lower at a cooling rate of 10 ° C./sec or higher. In order to improve the powdering resistance, prevention of overalloying after the alloying treatment is particularly important, and for this purpose, the temperature region where alloying does not proceed after the molten zinc layer on the surface layer disappears by alloying heating ( Up to 300 ° C) up to 10 ° C /
It is necessary to cool at a cooling rate of sec or more to prevent overalloying.
【0023】[0023]
〔実施例1〕表1に示す成分組成の鋼を転炉で溶製し、
スラブ加熱温度:1150℃、熱延巻取温度:580℃
の条件で3.6mmまで熱間圧延した。この熱延板を通
常の方法で酸洗後、1.8mmまで冷間圧延し、次い
で、直火加熱炉タイプのCGLにおいて800℃で焼鈍
した後、片面60g/m2の付着量のめっきを施し、引
き続き合金化処理を施した。この合金化処理は、誘導加
熱方式の合金化炉において、炉出側の鋼板板温が500
℃となるようにして実施した。また、合金化が完了し溶
融亜鉛層が消滅した時点で、直ちに平均冷却速度25℃
/secで250℃まで冷却し、その後水冷した。この
ようにして得られた合金化溶融亜鉛めっき鋼板の表面外
観および各種特性を表2に示す。表2によれば、強度−
延性バランスおよび皮膜特性(表面外観)の観点から、
本発明成分鋼であるa〜d鋼が優れた特性を示すことが
判る。[Example 1] Steel having the composition shown in Table 1 was melted in a converter,
Slab heating temperature: 1150 ° C, hot rolling coiling temperature: 580 ° C
It hot-rolled to 3.6 mm on condition of. This hot-rolled sheet was pickled by a usual method, cold-rolled to 1.8 mm, then annealed at 800 ° C. in a direct-fired furnace type CGL, and then plated with an adhesion amount of 60 g / m 2 on one side. Then, alloying treatment was performed subsequently. In this alloying treatment, in the induction heating type alloying furnace, the steel plate temperature on the exit side of the furnace is 500
It carried out so that it might become (degreeC). In addition, when alloying is completed and the molten zinc layer disappears, the average cooling rate is 25 ° C immediately.
/ Sec to 250 ° C., and then water cooling. Table 2 shows the surface appearance and various characteristics of the galvannealed steel sheet thus obtained. According to Table 2, strength-
From the viewpoint of ductility balance and film characteristics (surface appearance),
It can be seen that the steels a to d, which are the component steels of the present invention, exhibit excellent properties.
【0024】[0024]
【表1】 [Table 1]
【0025】[0025]
【表2】 [Table 2]
【0026】〔実施例2〕表1のa〜d鋼を用い、合金
化ムラ発生に及ぼす熱延条件の影響を調べた。上記各鋼
をスラブ加熱温度および熱延巻取温度を種々変化させて
1.8mmまで熱間圧延した後、直火加熱炉タイプのC
GLにおいて850℃で焼鈍し、次いで、片面45g/
m2のめっきを施した後、誘導加熱方式の合金化処理炉
において合金化処理を施した。この合金化処理では炉出
側板温が500℃となるようにし、合金化が完了し溶融
亜鉛層が消滅した時点で直ちに平均冷却速度25℃/s
ecで250℃まで冷却し、その後水冷した。図4はこ
のようにして得られためっき鋼板について、その合金化
不均一性をスラブ加熱温度と巻取温度で整理して示した
ものである。図4によれば、本発明が規定する条件で熱
間圧延を行うことにより、熱延工程で生じる原板表面の
不均一性に起因した合金化異常が効果的に抑えられるこ
とが判る。なお、図4に記載したタイプ、タイプの
合金化異常の区別は図3に関して述べたものと同様であ
る。Example 2 Using the steels a to d in Table 1, the effect of hot rolling conditions on the occurrence of alloying unevenness was investigated. Each of the above steels was hot-rolled to 1.8 mm by variously changing the slab heating temperature and the hot rolling coiling temperature, and then a direct-fired furnace type C was used.
Annealed at 850 ° C in GL, then 45 g / side
After the plating of m 2 was performed, the alloying treatment was performed in the induction heating type alloying treatment furnace. In this alloying process, the furnace outlet plate temperature was set to 500 ° C., and when the alloying was completed and the molten zinc layer disappeared, the average cooling rate was 25 ° C./s immediately.
It was cooled to 250 ° C. by ec and then water-cooled. FIG. 4 shows the alloying nonuniformity of the plated steel sheet thus obtained, arranged by the slab heating temperature and the winding temperature. From FIG. 4, it can be seen that by performing hot rolling under the conditions specified by the present invention, alloying abnormalities caused by nonuniformity of the surface of the original plate in the hot rolling process can be effectively suppressed. The types shown in FIG. 4 and the types of alloying abnormalities are distinguished from each other in the same manner as described with reference to FIG.
【0027】〔実施例3〕表1のa〜d鋼を用い、鋼板
の強度に及ぼすCGL焼鈍温度の影響を調べた。上記各
鋼をスラブ加熱温度:1150℃、熱延巻取温度:58
0℃の条件で3.6mmまで熱間圧延した。この熱延板
を通常の方法で酸洗した後、1.2mmまで冷間圧延
し、次いで、直火加熱炉タイプのCGLにおいて780
〜900℃の範囲で焼鈍し、引き続き片面45g/m2
の付着量のめっきを施した後、誘導加熱方式の合金化炉
において合金化処理を行った。この合金化処理では、炉
出側板温が500℃となるようにし、合金化が完了し溶
融亜鉛層が消滅した時点で直ちに平均冷却速度25℃/
secで250℃まで冷却し、その後水冷した。図5
は、このようにして得られた合金化溶融亜鉛めっき鋼板
の引張強度を焼鈍温度で整理して示したものであり、2
相温度域での焼鈍温度を変えることにより強度レベルを
任意に変化させ得ることが判る。Example 3 Using the steels a to d in Table 1, the effect of the CGL annealing temperature on the strength of the steel sheet was examined. Slab heating temperature of each of the above steels: 1150 ° C., hot rolling coiling temperature: 58
It hot-rolled to 3.6 mm on condition of 0 degreeC. This hot-rolled sheet was pickled by a usual method, then cold-rolled to 1.2 mm, and then 780 in a direct-fired furnace type CGL.
Annealed in the range of up to 900 ° C, then one side 45g / m 2
After plating with the amount of deposit of, the alloying treatment was performed in the induction heating type alloying furnace. In this alloying treatment, the temperature on the outlet side of the furnace was set to 500 ° C., and when the alloying was completed and the molten zinc layer disappeared, the average cooling rate was 25 ° C. /
It was cooled to 250 ° C. in sec and then cooled with water. Figure 5
Shows the tensile strength of the alloyed hot-dip galvanized steel sheet thus obtained, arranged by annealing temperature.
It is understood that the strength level can be arbitrarily changed by changing the annealing temperature in the phase temperature range.
【0028】〔実施例4〕表1のb鋼を用い、耐パウダ
リング性に及ぼす合金化条件の影響を調べた。上記b鋼
をスラブ加熱温度:1150℃、熱延巻取温度:580
℃の条件で3.2mmまで熱間圧延した。この熱延板を
通常の方法で酸洗した後、0.8mmまで冷間圧延し、
次いで、直火加熱炉タイプのCGLで850℃で焼鈍
し、引き続き片面当り60g/m2の付着量のめっきを
施した後、誘導加熱方式の合金化炉において合金化処理
を行った。この合金化処理では炉出側板温と平均冷却速
度を種々変化させ、これらが耐パウダリング性に及ぼす
影響を調べた。表3に、得られた合金化溶融亜鉛めっき
鋼板の耐パウダリング性および表面外観を合金化条件と
ともに示す。これによれば、炉出側板温と合金化完了の
後の冷却速度が本発明条件を満足する場合にのみ、優れ
た耐パウダリング性と良好な表面外観が得られることが
判る。Example 4 Using the steel b in Table 1, the effect of alloying conditions on the powdering resistance was examined. Slab heating temperature of the above b steel: 1150 ° C., hot rolling coiling temperature: 580
It was hot-rolled to 3.2 mm under the condition of ° C. After pickling this hot-rolled sheet by a usual method, cold-rolling to 0.8 mm,
Then, it was annealed at 850 ° C. in a direct-fired furnace type CGL, followed by plating with an adhesion amount of 60 g / m 2 per side, and then an alloying treatment was performed in an induction heating type alloying furnace. In this alloying process, the temperature at the outlet side of the furnace and the average cooling rate were variously changed, and the effects of these on the powdering resistance were investigated. Table 3 shows the powdering resistance and surface appearance of the obtained galvannealed steel sheet together with alloying conditions. According to this, it is understood that excellent powdering resistance and a good surface appearance can be obtained only when the temperature at the exit side of the furnace and the cooling rate after completion of alloying satisfy the conditions of the present invention.
【0029】[0029]
【表3】 [Table 3]
【0030】〔実施例5〕表1のc鋼を用い、合金化加
熱方式の違いによる鋼板厚み方向の加熱状態の違いを鋼
板厚み方向硬度分布により調べた。上記c鋼をスラブ加
熱温度:1150℃、熱延巻取温度:580℃の条件で
1.6mmまで熱間圧延し、これを直火加熱炉タイプの
CGLで870℃で焼鈍した後、片面60g/m2の付
着量のめっきを施し、引き続き合金化処理を施した。こ
の合金化処理では誘導加熱方式とガス加熱方式を用い、
それぞれ出側板温が505℃となるよう加熱処理を行っ
た。各合金化処理において、合金化が完了し溶融亜鉛層
が消滅した時点で直ちに平均冷却速度25℃/secで
250℃まで冷却し、その後水冷した。図6は、得られ
た合金化溶融亜鉛めっき鋼板の板厚方向硬度分布を示し
たものであり、これによれば、ガス加熱方式では板厚方
向全体が加熱されるのに対し、誘導加熱方式では鋼板表
層部のみが優先的に加熱され、鋼板内部の加熱が抑えら
れていることが判る。Example 5 Using the steel c in Table 1, the difference in the heating state in the steel sheet thickness direction due to the difference in the alloying heating method was examined by the steel sheet thickness direction hardness distribution. The above c steel was hot-rolled to 1.6 mm under the conditions of slab heating temperature: 1150 ° C. and hot rolling coiling temperature: 580 ° C., and this was annealed at 870 ° C. in a direct-fired furnace type CGL, and then 60 g on one side. / M 2 of the deposited amount was applied, and then the alloying treatment was applied. In this alloying process, induction heating method and gas heating method are used.
Heat treatment was performed so that the outlet plate temperature was 505 ° C., respectively. In each alloying treatment, immediately after the alloying was completed and the molten zinc layer disappeared, the alloy was immediately cooled to 250 ° C. at an average cooling rate of 25 ° C./sec, and then water-cooled. FIG. 6 shows the hardness distribution in the thickness direction of the obtained galvannealed steel sheet. According to this, the gas heating method heats the entire thickness direction, whereas the induction heating method. It can be seen that, only the surface layer of the steel sheet is heated preferentially and the heating inside the steel sheet is suppressed.
【図1】図3に示すタイプの合金化異常が生じた合金
化めっき層断面の金属組織を示す顕微鏡拡大写真FIG. 1 is an enlarged photomicrograph showing a metal structure of a cross section of an alloyed plating layer in which an alloying abnormality of the type shown in FIG. 3 has occurred.
【図2】図3に示すタイプの合金化異常が生じた合金
化めっき層断面の金属組織を示す顕微鏡拡大写真FIG. 2 is an enlarged micrograph showing a metal structure of a cross section of an alloyed plating layer in which an alloying abnormality of the type shown in FIG. 3 has occurred.
【図3】熱延スラブ加熱温度および熱延巻取温度が合金
化異常に及ぼす影響を示したグラフFIG. 3 is a graph showing the effects of hot rolling slab heating temperature and hot rolling coiling temperature on alloying anomalies.
【図4】実施例2において、熱延スラブ加熱温度と熱延
巻取温度が合金化異常に及ぼす影響を示したグラフFIG. 4 is a graph showing the effects of hot rolling slab heating temperature and hot rolling coiling temperature on alloying anomalies in Example 2.
【図5】実施例3において、CGL焼鈍温度がめっき鋼
板の強度レベルに及ぼす影響を示したグラフFIG. 5 is a graph showing the effect of CGL annealing temperature on the strength level of the plated steel sheet in Example 3.
【図6】実施例5において、合金化処理の加熱方式が鋼
板の板厚方向硬度分布に及ぼす影響を示したグラフFIG. 6 is a graph showing the influence of the heating method of alloying treatment on the hardness distribution of the steel sheet in the plate thickness direction in Example 5.
───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.6 識別記号 庁内整理番号 FI 技術表示箇所 C22C 38/00 301 C22C 38/00 301T 38/24 38/24 C23C 2/40 C23C 2/40 (72)発明者 鷺山 勝 東京都千代田区丸の内一丁目1番2号 日本鋼管株式会社内 (56)参考文献 特開 昭56−51532(JP,A) 特開 昭56−163219(JP,A) 特開 昭58−58264(JP,A)─────────────────────────────────────────────────── ─── Continuation of the front page (51) Int.Cl. 6 Identification code Office reference number FI technical display location C22C 38/00 301 C22C 38/00 301T 38/24 38/24 C23C 2/40 C23C 2/40 ( 72) Inventor Masaru Sagiyama 1-2-1, Marunouchi, Chiyoda-ku, Tokyo Within Nippon Kokan Co., Ltd. (56) References JP-A-56-51532 (JP, A) JP-A-56-163219 (JP, A) Special Kaisho 58-58264 (JP, A)
Claims (1)
0.15〜0.35wt%、Mn:1.50〜2.00
wt%、P:0.05wt%以下、S:0.02wt%
以下、Sol.Al:0.03〜0.06wt%、N:
0.0070wt%以下、Cr:0.15〜0.25w
t%、V:0.050〜0.100wt%を含有し、残
部Feおよび不可避的不純物からなる組成を有する鋼
を、熱延スラブ加熱温度:1170℃以下、熱延巻取温
度:600℃以下の条件で熱間圧延し、必要に応じて冷
間圧延した後、連続溶融亜鉛めっきラインにおいて、A
c1変態点以上、Ac3変態点以下の温度で焼鈍した後めっ
きし、次いで、誘導加熱方式の合金化炉において炉出側
板温が450〜550℃となるよう合金化加熱処理を行
い、表層の溶融亜鉛層が消滅後、300℃以下の温度ま
でを10℃/sec以上の冷却速度で冷却することを特
徴とする強度−延性バランスおよび皮膜特性に優れた高
強度合金化溶融亜鉛めっき鋼板の製造方法。1. C: 0.08 to 0.14 wt%, Si:
0.15-0.35 wt%, Mn: 1.50-2.00
wt%, P: 0.05 wt% or less, S: 0.02 wt%
Below, Sol. Al: 0.03 to 0.06 wt%, N:
0.0070 wt% or less, Cr: 0.15-0.25w
steel containing t%, V: 0.050 to 0.100 wt% and having a composition consisting of balance Fe and unavoidable impurities, hot rolled slab heating temperature: 1170 ° C. or lower, hot rolled coiling temperature: 600 ° C. or lower In the continuous hot-dip galvanizing line, after hot rolling under the conditions
After annealing at a temperature of not less than c 1 transformation point and not more than Ac 3 transformation point, plating is performed, and then alloying heat treatment is performed in an induction heating type alloying furnace so that the furnace exit side plate temperature is 450 to 550 ° C. Of a high-strength galvannealed steel sheet excellent in strength-ductility balance and coating characteristics, characterized by cooling to a temperature of 300 ° C. or lower at a cooling rate of 10 ° C./sec or more after disappearance of the molten zinc layer of Production method.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP3295186A JP2565038B2 (en) | 1991-10-15 | 1991-10-15 | Method for producing high-strength galvannealed steel sheet with excellent strength-ductility balance and film properties |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP3295186A JP2565038B2 (en) | 1991-10-15 | 1991-10-15 | Method for producing high-strength galvannealed steel sheet with excellent strength-ductility balance and film properties |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH05106007A JPH05106007A (en) | 1993-04-27 |
| JP2565038B2 true JP2565038B2 (en) | 1996-12-18 |
Family
ID=17817323
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP3295186A Expired - Fee Related JP2565038B2 (en) | 1991-10-15 | 1991-10-15 | Method for producing high-strength galvannealed steel sheet with excellent strength-ductility balance and film properties |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP2565038B2 (en) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR100572179B1 (en) * | 1999-10-22 | 2006-04-18 | 제이에프이 스틸 가부시키가이샤 | High strength hot dip galvanized steel sheet with excellent workability and plating property and manufacturing method |
| JP4714404B2 (en) * | 2003-01-28 | 2011-06-29 | 新日本製鐵株式会社 | High strength thin steel sheet with excellent hydrogen embrittlement resistance and method for producing the same |
| KR100896608B1 (en) * | 2007-06-18 | 2009-05-08 | 주식회사 포스코 | High yield ratio high strength cold rolled steel sheet, hot dip galvanized steel sheet, alloyed zinc plated steel sheet and manufacturing method thereof |
| KR101153670B1 (en) * | 2008-12-26 | 2012-06-18 | 주식회사 포스코 | A Method for Alloying Cold-Rolled Steel Sheet |
| CN114351072B (en) * | 2021-12-29 | 2024-03-05 | 北华航天工业学院 | Production process of alloyed plated steel bar |
-
1991
- 1991-10-15 JP JP3295186A patent/JP2565038B2/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| JPH05106007A (en) | 1993-04-27 |
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