JPH0137470B2 - - Google Patents
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- Publication number
- JPH0137470B2 JPH0137470B2 JP59028715A JP2871584A JPH0137470B2 JP H0137470 B2 JPH0137470 B2 JP H0137470B2 JP 59028715 A JP59028715 A JP 59028715A JP 2871584 A JP2871584 A JP 2871584A JP H0137470 B2 JPH0137470 B2 JP H0137470B2
- Authority
- JP
- Japan
- Prior art keywords
- tensile strength
- strength
- steel
- gcs
- dip galvanizing
- 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
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Description
技術分野
溶接構造物として加工組立てをした上で溶融亜
鉛めつき浴中に浸漬して亜鉛めつきを施し供用さ
れる溶接構造用、高張力鋼における溶接部とくに
溶接熱影響部(HAZと略す)に生じ勝ちな、溶
融亜鉛めつきに基く割れ感受性(GCS性という)
の低減に関してこの明細書で述べる技術内容は、
とくに引張強さが60Kgf/mm2以上の高張力鋼につ
いて、生産性阻害を伴うことのない耐GCS性の
著大な改善を目指した開発成果の新規な提案に係
わる。
背景技術
鉄鋼構造物の防錆性又はさらに美観とくに塗装
性の観点において溶融亜鉛めつき処理は有用であ
り、従来広く用いられている。近年に至り、鉄鋼
構造物の大型化ないしは軽量化の強い要請の下
に、上記めつき処理を施すべき溶接構造物用鋼材
の高強度化の気運が昂まりつつあるが、高張力鋼
にあつては、それもとくに60Kgf/mm2を超えるレ
ベルの鋼材は、溶接粗立てを経て、溶融亜鉛浴中
への浸漬による亜鉛めつき処理が施される際に、
HAZでのいわゆるめつき割れないしは、液体金
属ぜい化と呼ばれる、粒界割れの多発傾向が、殊
のほか著しい。
それと云うのは、溶接構造物の大型化、複雑化
の下に溶接施工に伴う残留応力が、引張り強さの
高い材料程、より著大となつて、上記割れを助長
する一因ともなるからである。
従つて耐GCS性の低減のため、溶接の際にお
ける残留応力や、溶融亜鉛めつき浴への浸漬時の
熱応力を軽減するように、溶接施工条件や浸漬条
件について考慮が加えられ、また応力除去焼鈍処
理も行われているが、経済性ないしは、母材特性
を損うなど、根本的解決策とは云えず、鋼材その
ものの改善が必要とされる所以である。
従来技術とその問題点
耐GCS性を必要とする溶接構造用鋼の成分組
成上の配慮については、特開昭57−104656号およ
び同58−84959号両公報において、0.005〜0.05wt
%(以下単に%で示す)のTi単独又は0.005〜
0.03%Tiと、0.02〜0.09%のVとの複合含有によ
る、耐GCS性の向上が開示されているが、この
ような含Ti鋼は、よく知られているように連続
鋳造法の活用に際し鋳肌表面にいわゆるスター割
れと呼ばれる表面欠陥が多発し、熱間圧延に先立
つ表面手入を必要とする工程上の不利があるのみ
ならず、該手入による歩留り低下も不可避なとこ
ろに問題を残している。
発明の目的
Ti添加に随伴する上掲した不利のない成分組
成において、とくに60Kgf/mm2以上の引張強さを
もつ高張力溶接構造用鋼における耐GCS性を、
有利に改善することがこの発明の目的である。
発明の構成
上記目的は、次の事項を骨子とする成分調整の
下で、有利に充足される。
すなわち、C:0.08〜0.15wt%、Si:0.10〜
0.50%、Mn:1.00〜2.00%、Zr:0.012〜0.030%、
sol Al:0.005〜0.100%、Nb:0.01〜0.10%及び
V:0.01〜0.10%を、次式
265−293C−21Si−96Mn−370V
−410Nb−35Al+534Zr≧40 …(1)
の関係において含有し、残部はFeおよび不純物
元素の組成である。
この発明の実際的な展開においては、0.05〜
1.00%の範囲内にて、Ni、Cu、CrおよびMoを鋼
質の強じん化成分として、また0.0005〜0.0040%
のBを焼入性の増強による強化成分、さらには
0.0005〜0.0050%のCeおよびCaを、粒成長の抑制
ないしは介在物形態制御によるじん性改善成分と
して、上記各群のうちより、選択して鋼中成分に
加えることがよりのぞましく、この場合において
各成分も含めた耐GCS性に及ぼす影響は次式で
あらわされる。
265−293C−21Si−96Mn−370V−410Nb
−35Al−18Ni−128Cu−94Cr−90Mo−2454B
+534Zr+1429Ce≧40 …(2)
なおCuについては上記範囲のうち比較的多量
の含有とするとき、Niと複合することがよりの
ぞましい。
この発明のポイントは、60Kgf/mm2をこえる引
張強さのレベルを確保することができる成分粗成
においてとくに0.012〜0.030%の範囲のZrを耐
GCS性の改善成分として含有することが、所期
の目的に適合するとの知見に由来している。
ちなみにZrについては上掲先行技術の前者に
て、介在物の形態制御元素として、0.15%まで、
清浄度を害しない限度でTiに併用することに言
及されてはいるけれども、ここに上記耐GCS性
に関するZrの直接の影響、寄与に何ら触れられ
てはいない。
この発明において、耐GCS性高張力鋼の成分
組成を限定した技術的根拠は、次の通りである。
C:0.08〜0.15%
Cは最も簡便に鋼の強さを上昇させるのに役立
つ成分であり、0.08%未満でその効果が期待され
ない一方、0.15%をこえると溶接性が低下し、目
的に適合しないことから0.08〜0.15%の範囲とす
る。
Si:0.10〜0.50%
Siは、脱酸作用の利用と、強度への寄与を目指
して0.10%以上を必要とするが、0.5%をこえる
と、耐GCS性に亜影響を及ぼし、また低温じん
性を劣化させるきらいがあるため、0.10〜0.50%
とする。
Mn:1.00〜2.00%
Mnも強さの確保のため、最低1.00%を必要と
し、一方2.00%をこえると耐GCS性を損う上、溶
接性や加工性など基本性能を害するので1.00〜
2.00%の範囲に制限する。
Zr:0.012〜0.030%
Zrは、この発明に従い、60Kgf/mm2以上の引
張強さの下での耐GCS性を、従来技術の説明で
触れたような不利を伴うことなく確保するのに役
立つ重要成分で、0.012%以上の含有量としたと
きHAZ組織の微細化の下で耐GCS性改善に新規
著効を奏するが0.030%をこえると、鋼の清浄度
に支障を伴い機械的性質、とくにじん性を劣化さ
せる不利を生じるので、0.012〜0.030%の範囲に
限定するを要する。
sol Al:0.005〜0.100%
Alは、脱酸作用と焼入れ性向上のため、0.005
%以上が必要であるが0.100%をこえると耐GCS
性溶接性の低下を来すので0.005〜0.100%とす
る。
NbおよびV:0.01〜0.10%
NbおよびVによる強さの増強には、0.01%を
必要する一方、0.10%をこえると、耐GCS性、溶
接性の低下を伴うので、それぞれ0.01〜0.10%と
する。
この発明の耐GCS性改善の前提としての高張
力化を耐GCS性の劣化を伴うことなくより有利
に実現するための、強じん化成分として有用な、
Ni、Cu、CrおよびMoは、何れも少くとも1種
にて0.05%以上を必要とするがNi、CuおよびCr
は1.00%をこえると、溶接性、熱間加工性が低下
し、また経済性の面でも不利であり、さらにMo
は、圧延時のオーステナイト粒を整粒化するとと
もに強じん化に役立つ効果の増進が、1.00%をこ
える過量添加で飽和に達し、経済的に不利なの
で、何れも1.00%に止めるべきである。
次にBは0.0005%程度以上の微量にて焼入性増
加に寄与するが0.0040%をこえると効果が飽和す
るほか、HAZの硬化が甚しくなるので、0.0005
〜0.004%の範囲が有用である。
Ceは、オキシサルフアイドと粒成長の抑制又
は硫化物の形態制御の各効果をもたらす0.0005%
以上の含有が必要であるが0.0005%をこえると清
浄度の亜化で機械的特性を損うおそれがあるので
0.0005〜0.0050%の範囲に限定される。
次に鋼中不純物としてのS、Pについてはそれ
ぞれ0.020%、0.030%以内が許容されるが、とく
にNは、0.012%をこえるとじん性劣化が著しい
ので、0.012%以下において低い程のぞましい。
上記の成分組成範囲において(1)又は(2)式に従う
成分調整を施した溶鋼を、通常の製鋼手段で得た
のち、造塊法又は連鋳法によるスラブ、ブルーム
又はビレツトについて、必要な圧延加工を常法に
従い施してこの発明の高張力鋼は製造され得る。
この構造用鋼は、溶接組立てののち溶融亜鉛め
つきが施れるところ、その際HAZに生じ勝ちな
割れの回避について以下のべる。
さて溶融亜鉛メツキ割れ性を次のようにして評
価した。
試験片は第1表に示す種々の化学成分の鋼板か
ら10mmφの丸棒を切り出し高周波加熱により
15KJ/cmの溶接入熱量相当の熱サイクルを付与
した後、円周切欠き加工を施したものである。
Technical field Welded parts, especially weld heat affected zones (HAZ) in high-strength steel, for welded structures that are processed and assembled as welded structures and then immersed in a hot-dip galvanizing bath to galvanize them. Cracking susceptibility due to hot-dip galvanizing (also known as GCS)
The technical content described in this specification regarding the reduction of
In particular, it is concerned with new proposals based on development results aimed at significantly improving GCS resistance without hindering productivity, especially for high-strength steels with a tensile strength of 60 Kgf/mm 2 or higher. BACKGROUND ART Hot-dip galvanizing is useful from the viewpoint of rust prevention or aesthetics, particularly paintability, of steel structures, and has been widely used in the past. In recent years, due to the strong demand for larger and lighter steel structures, there has been a growing trend to increase the strength of steel materials for welded structures that should be subjected to the above-mentioned plating treatment. In particular, when steel materials with a strength exceeding 60Kgf/ mm2 are subjected to galvanizing treatment by immersion in a molten zinc bath after rough welding,
The tendency of frequent intergranular cracking, called plating cracking or liquid metal embrittlement, in HAZs is especially remarkable. This is because as welded structures become larger and more complex, the residual stress that accompanies welding becomes more significant for materials with higher tensile strength, which is one of the factors that promotes the above-mentioned cracking. It is. Therefore, in order to reduce GCS resistance, consideration must be given to welding conditions and immersion conditions to reduce residual stress during welding and thermal stress during immersion in a hot-dip galvanizing bath. Although removal annealing treatment has been carried out, it cannot be said to be a fundamental solution because it is not economical or impairs the properties of the base material, which is why the steel material itself needs to be improved. Prior art and its problems Regarding considerations regarding the composition of welded structural steel that requires GCS resistance, 0.005 to 0.05wt is discussed in both Japanese Patent Application Laid-Open No. 57-104656 and No. 58-84959.
% (hereinafter simply expressed as %) of Ti alone or 0.005~
It has been disclosed that the GCS resistance is improved due to the composite content of 0.03% Ti and 0.02 to 0.09% V, but as is well known, such Ti-containing steel is difficult to use when using the continuous casting method. Surface defects called so-called star cracks frequently occur on the surface of the cast surface, which not only poses a disadvantage in the process of requiring surface care prior to hot rolling, but also causes problems in that the yield inevitably decreases due to such care. I'm leaving it behind. Purpose of the Invention In a composition that does not have the above-mentioned disadvantages associated with Ti addition, it is possible to improve the GCS resistance of high-tensile welded structural steel, especially with a tensile strength of 60 Kgf/mm 2 or more.
It is an object of the invention to advantageously improve this. Structure of the Invention The above object is advantageously satisfied under the composition adjustment based on the following matters. That is, C: 0.08~0.15wt%, Si: 0.10~
0.50%, Mn: 1.00~2.00%, Zr: 0.012~0.030%,
sol Al: 0.005 to 0.100%, Nb: 0.01 to 0.10% and V: 0.01 to 0.10% in the relationship of the following formula 265−293C−21Si−96Mn−370V −410Nb−35Al+534Zr≧40…(1), The remainder is the composition of Fe and impurity elements. In practical development of this invention, 0.05~
Ni, Cu, Cr and Mo as steel toughening components within the range of 1.00%, and 0.0005 to 0.0040%
B is a reinforcing component that enhances hardenability, and
It is more desirable to select 0.0005 to 0.0050% of Ce and Ca from among the above groups and add them to the steel ingredients as toughness improving ingredients by suppressing grain growth or controlling inclusion morphology. In this case, the influence of each component on GCS resistance is expressed by the following equation. 265−293C−21Si−96Mn−370V−410Nb −35Al−18Ni−128Cu−94Cr−90Mo−2454B +534Zr+1429Ce≧40…(2) When Cu is contained in a relatively large amount within the above range, it is combined with Ni. It is more desirable to do so. The key point of this invention is that it can withstand Zr in the range of 0.012 to 0.030%, especially in the composition of ingredients that can ensure a tensile strength level exceeding 60Kgf/ mm2 .
This comes from the knowledge that its inclusion as a component to improve GCS properties is compatible with the intended purpose. By the way, regarding Zr, in the former of the above-mentioned prior art, it is used as an element to control the form of inclusions up to 0.15%.
Although it is mentioned that Zr can be used in combination with Ti to the extent that it does not impair cleanliness, there is no mention of the direct influence or contribution of Zr on the above-mentioned GCS resistance. In this invention, the technical basis for limiting the composition of the GCS-resistant high-strength steel is as follows. C: 0.08-0.15% C is a component that most easily helps increase the strength of steel, and if it is less than 0.08%, the effect is not expected, while if it exceeds 0.15%, weldability decreases and it is not suitable for the purpose. The range is set at 0.08 to 0.15%. Si: 0.10-0.50% Si is required to be 0.10% or more to utilize deoxidizing effect and contribute to strength, but if it exceeds 0.5%, it will have a sub-effect on GCS resistance and will also cause low-temperature dust. 0.10 to 0.50% as it tends to deteriorate
shall be. Mn: 1.00 to 2.00% Mn also requires a minimum content of 1.00% to ensure strength. On the other hand, if it exceeds 2.00%, it will not only impair GCS resistance but also impair basic performance such as weldability and workability, so it should be 1.00 to 2.00%.
Limit to 2.00% range. Zr: 0.012-0.030% Zr helps to ensure GCS resistance under tensile strength of 60 Kgf/mm 2 or more according to the present invention without the disadvantages mentioned in the description of the prior art It is an important component, and when the content is 0.012% or more, it has a new remarkable effect on improving the GCS resistance under the refinement of the HAZ structure, but when it exceeds 0.030%, it affects the cleanliness of the steel and deteriorates the mechanical properties. In particular, since it has the disadvantage of deteriorating toughness, it is necessary to limit it to a range of 0.012 to 0.030%. sol Al: 0.005 to 0.100% Al is 0.005 for deoxidizing effect and improving hardenability.
% or more is required, but if it exceeds 0.100%, GCS resistance
Since it causes a decrease in weldability, it is set at 0.005 to 0.100%. Nb and V: 0.01 to 0.10% Nb and V require 0.01% to increase strength, but exceeding 0.10% is accompanied by a decrease in GCS resistance and weldability, so 0.01 to 0.10%, respectively. do. Useful as a toughening component to more advantageously achieve high tensile strength as a premise for improving GCS resistance of this invention without deteriorating GCS resistance.
Ni, Cu, Cr and Mo all require at least 0.05% or more of one kind, but Ni, Cu and Cr
Mo
In addition, the enhancement of the effect of sizing the austenite grains during rolling and strengthening them reaches saturation when added in excess of 1.00%, which is economically disadvantageous, so both should be limited to 1.00%. Next, B contributes to increasing hardenability in small amounts of about 0.0005% or more, but if it exceeds 0.0040%, the effect is saturated and the hardening of the HAZ becomes severe.
A range of ~0.004% is useful. Ce is 0.0005%, which has the effect of suppressing oxysulfide and grain growth or controlling the morphology of sulfides.
It is necessary to contain more than 0.0005%, but if it exceeds 0.0005%, the cleanliness may deteriorate and the mechanical properties may be impaired.
Limited to the range of 0.0005-0.0050%. Next, S and P as impurities in steel are allowed to be within 0.020% and 0.030%, respectively, but N in particular is preferably as low as 0.012% or less, as toughness deteriorates significantly when it exceeds 0.012%. Molten steel whose composition has been adjusted according to formula (1) or (2) within the above composition range is obtained by ordinary steelmaking means, and then rolled into slabs, blooms, or billets by the ingot-forming method or continuous casting method. The high tensile strength steel of the present invention can be manufactured by processing according to conventional methods. This structural steel can be hot-dip galvanized after welding assembly, and the following describes how to avoid the cracking that tends to occur in HAZ. Now, the cracking properties of hot-dip galvanizing were evaluated as follows. The test pieces were made by cutting 10mmφ round bars from steel plates with various chemical compositions shown in Table 1 and heating them with high frequency.
After applying a heat cycle equivalent to a welding heat input of 15 KJ/cm, a circumferential notch was processed.
【表】【table】
【表】
* ○:割れなし ×:割れあり
各試験片の切欠き部のみに亜鉛めつきを施し、
その亜鉛が溶融状態となる470℃で種々の静的負
荷応力をかけ、その応力で破断する時間を測定し
た。このときの負荷応力とメツキを施さない試験
片の470℃での引張り強さの比(パーセント表示)
R〓と、その時の破断時間の関係を第1図に示し
た。ここにR〓は、470℃でめつきなし試験片の引
張り強さに対して幾%の応力状態に保持して破断
するに至つたかを示すパラメーターで、このR〓
が少くとも40%で高ければ高い程、残留応力や熱
応力が大きいときでも割れ難いことを示す。
実操業でのメツキ浴浸漬時間を考慮し、400秒
でのR〓の値を求め化学成分と重回帰して、(1)、
(2)式の左辺各項の係数が求められた。
一方実溶接後のめつき処理での割れ状況との対
応をとるため、第2図に示す拘束継手を製作し、
溶融亜鉛めつき浴に浸漬後、熱影響部の割れを調
べた。
図中の1−1,1−2は試験ビード、また2−
1,2−2は拘束ビードであり3は試験板であ
る。試験板3は、片側が研削された板を十字に組
み、研削面同士の隅肉ビード1−1、黒皮同士の
隅肉ビード1−2となるように組み立てた。
試験板寸法は、板厚が15mmで、試験ビードの長
さ寸法L=50mm、また十字の各張出し長さl1=l2
=l3=l4=50mm、そして試験板3の全長W=150mm
である。拘束ビード2−1,2−2の各ビード数
はそれぞれ20である。
この拘束継手は溶融亜鉛メツキ浴に浸漬して試
験ビード1−1,1−2における割れ発生の有無
を確認し、その結果は第1表に併記したとおりで
ある。これから特許請求の範囲内の成分組成で、
かつ、(1)、(2)式の左辺の計算値につき
R〓≧40
が満たされれば拘束継手に割れが生じていないこ
とがわかる。
実施例
第2表に化学成分を示した比較材、発明材を真
空溶解によりそれぞれ100Kg鋼塊に溶製し、第2
表中、S13、S14及びS16は圧延ののち空冷し、
S11及びS12は圧延後加速冷却し、S15及びS17は
焼入れ焼戻し処理を施した。[Table] * ○: No cracks ×: Cracks Only the notch part of each test piece was galvanized.
Various static load stresses were applied at 470°C, when the zinc is in a molten state, and the time required for the zinc to break under the stress was measured. Ratio of the applied stress at this time to the tensile strength at 470℃ of the unplated test piece (expressed as a percentage)
The relationship between R〓 and the rupture time is shown in Figure 1. Here, R〓 is a parameter that indicates what percentage of the tensile strength of an unplated test piece was maintained at 470°C until it broke.
is at least 40%, and the higher the value, the more difficult it is to crack even when residual stress or thermal stress is large. Considering the immersion time in the plating bath in actual operation, find the value of R〓 at 400 seconds and perform multiple regression with the chemical components, (1),
The coefficients of each term on the left side of equation (2) were determined. On the other hand, in order to deal with cracking during the plating process after actual welding, a restraint joint as shown in Figure 2 was manufactured.
After immersion in a hot-dip galvanizing bath, cracks in the heat-affected zone were examined. 1-1 and 1-2 in the figure are test beads, and 2-
1 and 2-2 are restraining beads, and 3 is a test plate. The test plate 3 was assembled by assembling plates with one side ground in a cross pattern so that the fillet bead 1-1 was between the ground surfaces and the fillet bead 1-2 was between the black skins. The dimensions of the test plate are 15 mm thick, the length of the test bead L = 50 mm, and the length of each cross overhang l 1 = l 2
= l 3 = l 4 = 50 mm, and total length W of test plate 3 = 150 mm
It is. The number of each of the restraining beads 2-1 and 2-2 is 20. This constrained joint was immersed in a hot-dip galvanizing bath to check for cracks in the test beads 1-1 and 1-2, and the results are shown in Table 1. From now on, with the component composition within the scope of the claims,
Moreover, if R〓≧40 is satisfied for the calculated values on the left side of equations (1) and (2), it can be seen that no cracks have occurred in the restrained joint. Example The comparison material and the invention material whose chemical compositions are shown in Table 2 were each melted into a 100 kg steel ingot by vacuum melting.
In the table, S13, S14 and S16 are air cooled after rolling.
S11 and S12 were subjected to accelerated cooling after rolling, and S15 and S17 were subjected to quenching and tempering treatment.
【表】【table】
【表】
* ○:割れなし、×:割れあり
** 加速冷却材
*** 焼入れ焼もどし材 他は空冷材
第2表には鋼材の引張り強さ、じん性と、この
発明に従う回帰式によるR〓値および上述した拘
束継手試験での割れの検査結果を併記した。
拘束継手の製作は第2図につきすでに述べたよ
うに行い脱脂、酸洗、フラツクス処理後455℃の
溶融亜鉛浴中に6分浸漬して得られためつきを除
去した後熱影響部での割れ検査を行つた。
この表から明らかなようにこの発明の成分で回
帰式によるR〓値が40を超える発明鋼はすべて引
張強さ60Kgf/mm2以上であり、しかも拘束継手の
熱影響部にも割れは生じていない。
発明の効果
60Kgf/mm2以上の引張強さをもつ溶接構造用鋼
につき、その溶接施工を経たのちに施される溶融
亜鉛めつき処理に伴うHAZ部の割れに対する感
受性が、連続鋳造の適用における表面欠陥を随伴
するうれいなく、有利に軽減される。[Table] * ○: No cracking, ×: Cracking ** Accelerated cooling material *** Quenched and tempered material Others are air-cooled materials Table 2 shows the tensile strength and toughness of steel materials and the regression equation according to the present invention. The R value and the crack inspection results from the above-mentioned restrained joint test are also listed. The restraint joint was manufactured as already described in Figure 2, and after degreasing, pickling, and flux treatment, it was immersed in a 455°C molten zinc bath for 6 minutes to remove the resulting buildup, and then cracks in the heat-affected zone were removed. I conducted an inspection. As is clear from this table, all the invented steels with components of this invention whose R value exceeds 40 based on the regression equation have a tensile strength of 60 Kgf/mm2 or more , and furthermore, no cracks have occurred in the heat affected zone of the restrained joint. do not have. Effects of the invention For welded structural steel with a tensile strength of 60Kgf/mm2 or more , the susceptibility to cracking of the HAZ part due to the hot-dip galvanizing treatment applied after welding has been improved in the application of continuous casting. Concomitant surface defects are advantageously reduced.
第1図:R〓値と破断時間の関係グラフ、第2
図:拘束継手割れ試験体の正面図と側面図であ
る。
Figure 1: Relationship graph between R value and rupture time, 2nd
Figure: Front view and side view of a restrained joint crack test specimen.
Claims (1)
不可避的不純物であつて、引張り強さ60Kgf/mm2
以上であることを特徴とする耐溶融亜鉛めつき割
れ性に優れる溶接構造物用高張力圧延鋼材。 2 C:0.08〜0.15wt%、 Si:0.10〜0.50wt%、 Mn:1.00〜2.00wt%、 Zn:0.012〜0.030wt%、 sol Al:0.005〜0.100wt%、 Nb:0.01〜0.10wt%及び、 V:0.01〜0.10wt% と、さらに0.05〜1.00wt%のNi、Cu、Cr、Moの
1種または2種以上を、次式 265−293C−21Si−96Mn+534Zr−35Al− 410Nb−370V−18Ni−128Cu−94Cr −90Mo≧40 の関係において含有し残部は実質的にFeおよび
不可避的不純物であつて、引張り強さ60Kgf/mm2
以上であることを特徴とする耐溶融亜鉛めつき割
れ性に優れる溶接構造物用高張力圧延鋼材。 3 C:0.08〜0.15wt%、 Si:0.10〜0.50wt%、 Mn:1.00〜2.00wt%、 Zr:0.012〜0.030wt%、 sol Al:0.005〜0.100wt%、 Nb:0.01〜0.10wt%及び、 V:0.01〜0.10wt% とさらにB:0.0005〜0.0040wt%を、次式 265−293C−21Si−96Mn+534Zr −35Al−410Nb−370V−2454B≧40 の関係において含有し残部は実質的にFeおよび
不可避的不純物であつて、引張り強さ60Kgf/mm2
以上であることを特徴とする耐溶融亜鉛めつき割
れ性に優れる溶接構造物用高張力圧延鋼材。 4 C:0.08〜0.15wt%、 Si:0.10〜0.50wt%、 Mn:1.00〜2.00wt%、 Zr:0.012〜0.030wt%、 sol Al:0.005〜0.100wt%、 Nb:0.01〜0.10wt%及び、 V:0.01〜0.10wt% とさらに0.05〜1.00wt%のNi、Cu、Cr、Moの1
種または2種以上並びに、 0.0005〜0.0050wt%のCeを、 265−293C−21Si−96Mn+534Zr −35Al−410Nb−370V−18Ni−128Cu −94Cr−90Mo+1429Ce≧40 の関係において含有し残部は実質的にFeおよび
不可避的不純物であつて、引張り強さ60Kgf/mm2
以上であることを特徴とする耐溶融亜鉛めつき割
れ性に優れる溶接構造物用高張力圧延鋼材。[Claims] 1 C: 0.08-0.15wt%, Si: 0.10-0.50wt%, Mn: 1.00-2.00wt%, Zr: 0.012-0.030wt%, sol Al: 0.005-0.100wt%, Nb: It contains 0.01 to 0.10 wt% and V: 0.01 to 0.10 wt% in the relationship of the following formula 265-293C-21Si-96Mn+534Zr-35Al-410Nb-370V≧40, and the remainder is substantially Fe and inevitable impurities. Tensile strength 60Kgf/mm 2
A high-strength rolled steel material for welded structures having excellent hot-dip galvanizing cracking resistance, which is characterized by the above properties. 2 C: 0.08-0.15wt%, Si: 0.10-0.50wt%, Mn: 1.00-2.00wt%, Zn: 0.012-0.030wt%, sol Al: 0.005-0.100wt%, Nb: 0.01-0.10wt% and , V: 0.01 to 0.10wt% and further 0.05 to 1.00wt% of one or more of Ni, Cu, Cr, Mo, and the following formula 265−293C−21Si−96Mn+534Zr−35Al− 410Nb−370V−18Ni −128Cu−94Cr −90Mo≧40, the remainder is substantially Fe and unavoidable impurities, and has a tensile strength of 60Kgf/mm 2
A high-strength rolled steel material for welded structures having excellent hot-dip galvanizing cracking resistance, which is characterized by the above properties. 3 C: 0.08-0.15wt%, Si: 0.10-0.50wt%, Mn: 1.00-2.00wt%, Zr: 0.012-0.030wt%, sol Al: 0.005-0.100wt%, Nb: 0.01-0.10wt% and , V: 0.01 to 0.10wt% and B: 0.0005 to 0.0040wt% in the relationship of the following formula 265-293C-21Si-96Mn+534Zr-35Al-410Nb-370V-2454B≧40, and the remainder is substantially Fe and Unavoidable impurities, tensile strength 60Kgf/mm 2
A high-strength rolled steel material for welded structures having excellent hot-dip galvanizing cracking resistance, which is characterized by the above properties. 4 C: 0.08-0.15wt%, Si: 0.10-0.50wt%, Mn: 1.00-2.00wt%, Zr: 0.012-0.030wt%, sol Al: 0.005-0.100wt%, Nb: 0.01-0.10wt% and , V: 0.01~0.10wt% and further 0.05~1.00wt% of Ni, Cu, Cr, Mo.
Contains one or more species and 0.0005 to 0.0050 wt% of Ce in the relationship 265−293C−21Si−96Mn+534Zr −35Al−410Nb−370V−18Ni−128Cu −94Cr−90Mo+1429Ce≧40, and the remainder is substantially Fe. and unavoidable impurities, with a tensile strength of 60Kgf/mm 2
A high-strength rolled steel material for welded structures having excellent hot-dip galvanizing cracking resistance, which is characterized by the above properties.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2871584A JPS60181254A (en) | 1984-02-20 | 1984-02-20 | High tension steel having superior resistance to cracking due to hot dip galvanizing |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2871584A JPS60181254A (en) | 1984-02-20 | 1984-02-20 | High tension steel having superior resistance to cracking due to hot dip galvanizing |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS60181254A JPS60181254A (en) | 1985-09-14 |
| JPH0137470B2 true JPH0137470B2 (en) | 1989-08-07 |
Family
ID=12256138
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2871584A Granted JPS60181254A (en) | 1984-02-20 | 1984-02-20 | High tension steel having superior resistance to cracking due to hot dip galvanizing |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS60181254A (en) |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS4986212A (en) * | 1972-12-23 | 1974-08-19 | ||
| US3963531A (en) * | 1975-02-28 | 1976-06-15 | Armco Steel Corporation | Cold rolled, ductile, high strength steel strip and sheet and method therefor |
| CA1067060A (en) * | 1975-08-25 | 1979-11-27 | Ford Motor Company Of Canada | Equilibrium catalyst |
| JPS5356120A (en) * | 1976-11-02 | 1978-05-22 | Nippon Steel Corp | Production of high tensile bolt for low temperature service |
| JPS6020447B2 (en) * | 1981-03-31 | 1985-05-22 | 住友金属工業株式会社 | Method for manufacturing low carbon aluminum killed steel with excellent nitrate stress corrosion cracking resistance |
-
1984
- 1984-02-20 JP JP2871584A patent/JPS60181254A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS60181254A (en) | 1985-09-14 |
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