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JPH0430464B2 - - Google Patents
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JPH0430464B2 - - Google Patents

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Publication number
JPH0430464B2
JPH0430464B2 JP11754086A JP11754086A JPH0430464B2 JP H0430464 B2 JPH0430464 B2 JP H0430464B2 JP 11754086 A JP11754086 A JP 11754086A JP 11754086 A JP11754086 A JP 11754086A JP H0430464 B2 JPH0430464 B2 JP H0430464B2
Authority
JP
Japan
Prior art keywords
concrete
less
salt
reinforcing bars
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
Application number
JP11754086A
Other languages
Japanese (ja)
Other versions
JPS62274050A (en
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed filed Critical
Priority to JP11754086A priority Critical patent/JPS62274050A/en
Priority to CA000529832A priority patent/CA1292135C/en
Priority to AU68865/87A priority patent/AU568260B2/en
Priority to GB8704153A priority patent/GB2186886B/en
Publication of JPS62274050A publication Critical patent/JPS62274050A/en
Priority to US07/148,138 priority patent/US4836981A/en
Publication of JPH0430464B2 publication Critical patent/JPH0430464B2/ja
Granted legal-status Critical Current

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Description

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

(産業上の利用分野) 本発明は、海浜地帯に設置されるコンクリート
建造物、海洋に設置されるコンクリート構造物
等、および海塩粒子、海水の飛沫に曝らされる鉄
筋コンクリート構造物、コンクリート橋などに使
用され、その劣化防止作用が飛躍的に優れた耐海
水鉄筋に関するものである。 (従来の技術) 最近、海砂を使用した鉄筋コンクリート建築物
や海浜地帯に設置されたコンクリート建造物、コ
ンクリート橋のヒビ割れ劣化が各方面で問題にな
つており、種々の防止法が提案されたり、実施に
移されている。 このコンクリート劣化の最大の原因は海砂中に
含まれている塩分や、海浜地帯、海洋でコンクリ
ート壁を浸透してくる海塩粒子に基づく塩分によ
つてコンクリート中に埋設された鉄筋が腐食し、
その体積が約2.2倍になるため、その膨脹力に耐
え切れなくなつて埋設鉄筋に沿つたコンクリート
に亀裂が発生する。その亀裂が0.2mm以上になる
と外部の腐食因子たる酸素や、塩分、空気中の炭
酸ガスがこの亀裂を通してより容易に内部の埋設
鉄筋付近に浸透し、さらに一層鉄筋の腐食を助長
したり、コンクリートの中性化を促進してコンク
リートの劣化を早めることになる。 本発明者らはこのようなコンクリートの劣化を
防止するために鉄筋自体の化学組成を制御し、鉄
筋自体の耐塩性を向上する研究を実施し、その成
果として耐塩性を著しく向上したコンクリート用
鉄筋(特開昭57−48054号公報、特開昭59−44457
号公報)を開発し、これらの内容はすでに他の各
方面でも公表されている。 (“OFFSHORE GOTEBORG‘81“PaperNo.
42Goteborg SWEDEN 1981年、“セメントコン
クリート”No.434(1983)P.23/31、“コロージヨ
ン オブ ラインフオースメント インコンクリ
ート コンストラクシヨン(Corrosion of
Reinforcement in Concrete Construction)”
P.419 1983年、“建築の技術施工”1985年No.229号
1月号P155/164、彰国社)。 又、鉄筋自体の耐塩性向上に寄与する鉄筋の鋼
成分の初期の段階での耐塩機構についても、これ
らの公表論文の中に詳細に記載されている。 (発明が解決しようとする課題) 本発明は従来の耐塩性コンクリート鉄筋の開発
を軸にして最近、とくに問題となつてきたコンク
リート壁を浸透してくる海塩粒子や海水飛沫等の
フリーなCl-の状態で存在する塩分による鉄筋の
腐食とそれにともなうコンクリートの亀裂発生お
よび劣化を防止することを目的とするものであ
る。 現在各方面で問題となつている10年以上経過し
たコンクリート構造物の埋設鉄筋近傍のフリー塩
分は厳しい海洋環境ではNaCl換算で1.0%にも達
して鉄筋の著しい腐食とそれに伴うコンクリート
の亀裂発生、成長を惹き起こしている。したがつ
てこのような高濃度の塩分でも埋設鉄筋棒鋼の腐
食が完全に停止し、コンクリートの亀裂発生を停
止することが望ましい。 (課題を解決するための手段) 本発明の前記の目的は下記のとおりの構成の鉄
筋棒鋼を提供することによつて達成される。 (1) C;1.0%以下、Si;0.25%以下、Mn;2.0%
以下、Al;7.0〜20.0%、P;0.015%以下、
S;0.005%以下、Cr;0.5超〜5.5%を含有し、
残部鉄および不可避的不純物からなる耐海水鉄
筋棒鋼。 (2) C;1.0%以下、Si;0.25%以下、Mn;2.0%
以下、Al;7.0〜20.0%、P;0.015%以下、
S;0.005%以下、Cr;0.5超〜5.5%、さらに
Ti、Nbを単独あるいは併用して0.01〜0.5%含
有し、残部鉄および不可避的不純物からなる耐
海水鉄筋棒鋼。 本発明の最大の特徴は鋼中にAlを7.0〜20.0%
と多量に含有させ、高濃度の塩分に曝らされるコ
ンクリート中の埋設鉄筋に強力な不働態被膜を生
成させ、発錆を殆んど皆無にし、コンクリートの
劣化を完全に防止させることにある。すなわち従
来の発明の如く、錆の成長を抑制するという思想
ではなく、上記のような高濃度の塩分でも錆の発
生を皆無とするかないし抑制するようにしたもの
である。この原因については現在、検討中であり
明瞭なことは判明しないが、本発明による合金か
ら溶け出したAl3+がCl-と反応して生成した
AlCl3が水中のOH-と反応して直ちに極めて安定
なAl(OH)3に変化し、これが成長し、腐食因子
を遮断することにあると推定される。このことは
3.6%NaCl含有のPH12のCa(OH)2水溶液中での鉄
筋の表面電位が日数の経過につれて急速に貴の方
にずれていくことでも立証される。 以下に本発明における各成分の限定理由を説明
する。 C量を1.0%以下に限定した理由はC量が1.0%
を超えると脆化を惹き起こすためである。C量は
低い方がよく、好ましくは0.1%以下である。 Mn量を2.0%以下に限定した理由は2.0%を超
えると脆化を惹き起こすためで、好ましい範囲は
0.8%以下である。より好ましくは、0.3%以下で
ある。 Si量を0.25%以下とした理由はSi量が0.25%を
超えると鋼中のセメンタイトのグラフアイト化を
著るしく促進し加工性が劣化するためである。一
般にSi量を下げれば下げるほど錆発生を低減させ
るのでSi量の低い方が望ましい。最も望ましい範
囲はSi量0.05%未満である。 Alは本発明のカギを握る重要な元素で、とく
に極めて高濃度の塩分でも錆発生を抑制する効果
がある。この効果はAl量7.0%未満では期待でき
ず、20.0%超では経済的に不利になるのみならず
金属間化合物を生成して脆化する場合がある。最
も好ましい範囲はAl量8.0%以上18%以下の範囲
である。 Pを0.015%以下とした理由は、P0.015%超で
はコンクリートのようなアルカリ性雰囲気で錆生
成を抑制する効果がなく、むしろ助長する傾向が
あるためである。 Cr量を0.5%超とした理由は、Al量が7.0%以上
の場合、熱間圧延性能が向上するためであるが、
5.5%を超えると逆に脆化する場合が認められた
のでCr量を0.5超〜5.5%とした。最も好ましい範
囲は0.7〜2.0%の範囲である。 S量を0.005%以下と限定した理由は、錆の発
生起源であるMnS量を減らすことにあり、この
S量低下のために脱硫剤として使用されるCa化
合物、希土類元素によりMnSが(Mn、Ca)S等
に変化することによる耐食性向上効果も期待でき
る。また鋼中のS量を低下するために上記のよう
な操業を行なうことは常識となつているので、若
干のCa、Ce等が混入してくることがあるが、こ
れらの元素は耐食性などに悪影響を及ぼすもので
はないので、脱硫のために添加される量程度の混
入は差し支えがない。 本発明においては、上記の基本的な成分に加え
て、さらにTi、Nbを単独あるいは併用して0.01
〜0.5%の範囲で含有させることによつて、鉄筋
の強度等の特性を向上させることができる。 特に本発明のようにAlを多量に含有させた場
合に、固溶度の低下するCを炭化物とすることに
有利に作用する。 また、本発明の鋼の塩分に対する耐腐食性とコ
ンクリートの亀裂発生および劣化防止の性能は、
前記の基本的な成分系によつて良好に保たれるた
め、微量成分として添加されるV、W、Co、Mo
は、悪影響を及ぼすものではないので、0.5%以
下の存在は差し支えがない。 本発明に従い前記の化学成分で構成された鋼
は、転炉、電気炉等で溶製され、次いで造塊、分
塊の工程を経るか、あるいは連続鋳造後、圧延さ
れた後に必要に応じてパテンテイング等の熱処理
が施され、線引きされた鉄筋として使用に供され
る。又、必要に応じて亜鉛メツキ、有機被覆を施
すこともできる。 (実施例) 実施例 1 表1に記載した成分の鋼を真空溶解炉で溶製
し、造塊、分塊後線引きした鉄筋と従来鋼からな
る鉄筋との成分および腐食試験結果を示した。 準備した鉄筋の中央部より幅25mm×長さ60mm×
厚さ2mmの試片を採取し、機械研削して表面を研
磨した。 他方、コンクリートの主成分であるCaOを3.6
%NaCl水溶液中に溶解させてPH12のCa(OH)2
NaCl水溶液を準備した。 しかる後、前記のように表面研削し、側面と裏
面をシリコンレジンで被覆した試片を脱脂後、乾
燥し、直ちに上記のCa(OH)2+NaCl水溶液中に
浸漬した。なお試験中は液の表面を流動パラフイ
ンでシールし、3日毎に液を置換して20日間連続
浸漬し、錆の発生状況を観察した。 表中(A)は錆の発生面積(%)、表中(B)は局部腐
食の深さmmを示す。 実施例 2 NaClを1.0%含んだ砂、ポルトランドセメン
ト、水、砂利からなるコンクリートモルタルに表
1の成分からなる熱延鉄筋(9mmφ)を埋め込
み、28日間常温養生した後、海浜地帯に1年間曝
露した。 なお、コンクリートの水セメント比は0.60、カ
ブリ厚さは2cmとした。 1年間曝露後コンクリートを破砕して鉄筋の発
錆状況を調べた。その結果を表1中の(C)に示し
た。 表1の(A),(B),(C)から本発明の鉄筋はコンクリ
ート中の塩分が砂中NaCl換算で1.0%の高濃度、
水中で3.6%NaClの高濃度でも錆発生が皆無であ
ることが明瞭に認められ、錆発生、錆成長に伴な
うコンクリートの劣化を完全に停止できることが
判つた。従つて、極めて厳しい海洋環境において
もコンクリートの劣化を完全に抑止することが推
定される。 実施例 3 表2に示す成分の熱延鋼板から引張試験片を準
備し、JIS Z 2241に規定する方法で引試験を行
つた。その結果を表2に示した。
(Industrial Application Field) The present invention is applicable to concrete structures installed in coastal areas, concrete structures installed in the ocean, reinforced concrete structures exposed to sea salt particles and seawater spray, and concrete bridges. This article relates to seawater-resistant reinforcing bars that are used in such applications and have dramatically superior anti-deterioration properties. (Prior art) Recently, cracking and deterioration of reinforced concrete buildings using sea sand, concrete buildings installed in coastal areas, and concrete bridges has become a problem in various fields, and various prevention methods have been proposed. , has been put into practice. The biggest cause of this concrete deterioration is that the reinforcing bars embedded in the concrete corrode due to salt contained in sea sand and sea salt particles that permeate concrete walls in seashore areas and the ocean. ,
As its volume increases by approximately 2.2 times, it becomes unable to withstand the expansion force and cracks occur in the concrete along the buried reinforcing bars. If the crack is 0.2 mm or more, external corrosion factors such as oxygen, salt, and carbon dioxide gas in the air will more easily penetrate through the crack to the area around the buried reinforcing steel, further promoting corrosion of the reinforcing steel and causing concrete damage. This will accelerate the carbonation of concrete and accelerate the deterioration of concrete. In order to prevent such deterioration of concrete, the present inventors conducted research to improve the salt resistance of the reinforcing bars themselves by controlling the chemical composition of the reinforcing bars themselves, and as a result of their research, they developed reinforcing bars for concrete with significantly improved salt resistance. (Unexamined Japanese Patent Publication No. 57-48054, Unexamined Japanese Patent Publication No. 59-44457
The contents have already been published in various other areas. (“OFFSHORE GOTEBORG'81“Paper No.
42Goteborg SWEDEN 1981, “Cement Concrete” No.434 (1983) P.23/31, “Corrosion of Reinforcement
Reinforcement in Concrete Construction)”
P.419 1983, “Architectural Technology and Construction” 1985 No.229 January issue P155/164, Shokokusha). In addition, the salt resistance mechanism of the steel components of reinforcing bars at an early stage, which contributes to improving the salt resistance of reinforcing bars themselves, is also described in detail in these published papers. (Problems to be Solved by the Invention) The present invention focuses on the development of conventional salt-resistant concrete reinforcing bars, and aims to eliminate free chlorine from sea salt particles and seawater splashes that penetrate concrete walls, which has recently become a particular problem. The purpose is to prevent the corrosion of reinforcing bars due to salt present in - conditions, and the accompanying cracking and deterioration of concrete. Free salt near the buried reinforcing bars of concrete structures that are more than 10 years old, which is currently a problem in various fields, can reach up to 1.0% in terms of NaCl in the harsh marine environment, leading to severe corrosion of the reinforcing bars and the resulting cracks in the concrete. It is causing growth. Therefore, it is desirable to completely stop the corrosion of buried reinforcing steel bars even with such high concentrations of salt, and to stop the occurrence of cracks in concrete. (Means for Solving the Problems) The above object of the present invention is achieved by providing a reinforcing steel bar having the following configuration. (1) C: 1.0% or less, Si: 0.25% or less, Mn: 2.0%
Below, Al: 7.0 to 20.0%, P: 0.015% or less,
Contains S: 0.005% or less, Cr: more than 0.5 to 5.5%,
Seawater-resistant reinforcing steel bar consisting of residual iron and unavoidable impurities. (2) C: 1.0% or less, Si: 0.25% or less, Mn: 2.0%
Below, Al: 7.0 to 20.0%, P: 0.015% or less,
S; 0.005% or less, Cr; more than 0.5 to 5.5%, and
A seawater-resistant reinforcing steel bar containing 0.01 to 0.5% of Ti and Nb, either alone or in combination, with the remainder being iron and unavoidable impurities. The biggest feature of the present invention is that the steel contains 7.0 to 20.0% Al.
The purpose is to contain a large amount of salt to form a strong passive film on the buried reinforcing bars in concrete that are exposed to high concentrations of salt, almost eliminating rusting and completely preventing concrete deterioration. . That is, unlike conventional inventions, the idea is not to suppress the growth of rust, but rather to eliminate or suppress the generation of rust even in the presence of high concentrations of salt as described above. The cause of this is currently under investigation and is not clear, but it is believed that Al 3+ dissolved from the alloy of the present invention reacts with Cl - and is generated.
It is presumed that AlCl 3 reacts with OH - in water and immediately changes to extremely stable Al(OH) 3 , which grows and blocks corrosion factors. This thing is
This is also evidenced by the fact that the surface potential of reinforcing steel in an aqueous solution of Ca(OH) 2 at PH12 containing 3.6% NaCl rapidly shifts toward you as days pass. The reasons for limiting each component in the present invention will be explained below. The reason for limiting the C content to 1.0% or less is that the C content is 1.0%.
This is because exceeding this value causes embrittlement. The lower the C content, the better, and preferably 0.1% or less. The reason why the Mn content is limited to 2.0% or less is that exceeding 2.0% causes embrittlement, so the preferred range is
It is 0.8% or less. More preferably, it is 0.3% or less. The reason why the amount of Si is set to 0.25% or less is that if the amount of Si exceeds 0.25%, graphitization of cementite in the steel is significantly promoted and workability is deteriorated. In general, the lower the amount of Si, the less rust will occur, so a lower amount of Si is desirable. The most desirable range is a Si content of less than 0.05%. Al is an important element that holds the key to the present invention, and is particularly effective in suppressing rust formation even at extremely high concentrations of salt. This effect cannot be expected when the Al content is less than 7.0%, and when it exceeds 20.0%, it is not only economically disadvantageous but also may generate intermetallic compounds and become brittle. The most preferable range is an Al content of 8.0% or more and 18% or less. The reason why P is set to be 0.015% or less is that P exceeding 0.015% has no effect of suppressing rust formation in an alkaline atmosphere such as concrete, but rather tends to accelerate it. The reason why the Cr content is set to exceed 0.5% is that hot rolling performance improves when the Al content is 7.0% or more.
If it exceeded 5.5%, embrittlement was observed in some cases, so the Cr content was set at more than 0.5% to 5.5%. The most preferred range is 0.7-2.0%. The reason for limiting the amount of S to 0.005% or less is to reduce the amount of MnS, which is the source of rust. The effect of improving corrosion resistance by changing to Ca)S, etc. can also be expected. In addition, it is common knowledge to carry out the operations described above to reduce the amount of S in steel, so a small amount of Ca, Ce, etc. may be mixed in, but these elements have no effect on corrosion resistance. Since it does not have any adverse effects, there is no problem in mixing it in the same amount as added for desulfurization. In the present invention, in addition to the above basic components, Ti and Nb are used alone or in combination to
By containing it in the range of ~0.5%, properties such as strength of reinforcing bars can be improved. In particular, when a large amount of Al is contained as in the present invention, it is advantageous to convert C, whose solid solubility decreases, into carbide. In addition, the corrosion resistance of the steel of the present invention against salt and the performance of preventing cracking and deterioration of concrete are as follows:
Since V, W, Co, and Mo added as trace components are well maintained by the basic component system mentioned above,
does not have any negative effects, so its presence at 0.5% or less is acceptable. According to the present invention, the steel composed of the above chemical components is melted in a converter, electric furnace, etc., and then undergoes the steps of ingot making and blooming, or after continuous casting and rolling, if necessary. It is subjected to heat treatment such as patenting and used as drawn reinforcing steel. Further, galvanizing and organic coating can be applied as necessary. (Examples) Example 1 Steel with the components listed in Table 1 was melted in a vacuum melting furnace, and the components and corrosion test results of reinforcing bars made of ingots, bloomed and drawn, and reinforcing bars made of conventional steel are shown. Width 25mm x length 60mm x from the center of the prepared reinforcing bar
A specimen with a thickness of 2 mm was taken, and the surface was polished by mechanical grinding. On the other hand, CaO, the main component of concrete, is 3.6
% Ca(OH) 2 + dissolved in NaCl aqueous solution with pH 12
A NaCl aqueous solution was prepared. Thereafter, the surface of the sample was ground as described above, and the side and back surfaces were coated with silicone resin. The sample was degreased, dried, and immediately immersed in the above Ca(OH) 2 +NaCl aqueous solution. During the test, the surface of the liquid was sealed with liquid paraffin, the liquid was replaced every 3 days, and the samples were immersed continuously for 20 days to observe the occurrence of rust. (A) in the table shows the area where rust occurs (%), and (B) in the table shows the depth of local corrosion in mm. Example 2 Hot-rolled reinforcing bars (9 mmφ) made of the ingredients shown in Table 1 were embedded in a concrete mortar made of sand containing 1.0% NaCl, Portland cement, water, and gravel, and after curing at room temperature for 28 days, they were exposed to a seashore area for 1 year. did. The water-cement ratio of the concrete was 0.60, and the fog thickness was 2 cm. After one year of exposure, the concrete was crushed and the rusting status of the reinforcing bars was investigated. The results are shown in (C) in Table 1. From (A), (B), and (C) in Table 1, the reinforcing bars of the present invention have a high concentration of salt in the concrete of 1.0% in terms of NaCl in sand.
It was clearly observed that no rust occurred even in water at a high concentration of 3.6% NaCl, and it was found that the deterioration of concrete caused by rust occurrence and rust growth could be completely stopped. Therefore, it is presumed that deterioration of concrete is completely suppressed even in extremely harsh marine environments. Example 3 Tensile test pieces were prepared from hot-rolled steel sheets having the components shown in Table 2, and a tensile test was conducted according to the method specified in JIS Z 2241. The results are shown in Table 2.

【表】【table】

【表】【table】

【表】 (発明の効果) 本発明は今後ますます問題になる塩害、海水飛
沫に曝らされるコンクリート構造物の耐久性を維
持するのに画期的に有効なコンクリート用鉄筋と
して役立つものである。 本発明の耐海水鉄筋棒鋼を使用することによつ
て、コンクリート構造物の長寿命化、安定性の向
上を図ることが可能で、各種用途に使用すること
ができる。
[Table] (Effects of the invention) The present invention is useful as a groundbreakingly effective concrete reinforcing bar to maintain the durability of concrete structures exposed to salt damage and seawater spray, which will become increasingly problematic in the future. be. By using the seawater-resistant reinforcing steel bar of the present invention, it is possible to extend the lifespan and improve the stability of concrete structures, and it can be used for various purposes.

Claims (1)

【特許請求の範囲】 1 C;1.0%以下、Si;0.25%以下、Mn;2.0%
以下、Al;7.0〜20.0%、P;0.015%以下、S;
0.005%以下、Cr;0.5超〜5.5%を含有し、残部鉄
および不可避的不純物からなる耐海水鉄筋棒鋼。 2 C;1.0%以下、Si;0.25%以下、Mn;2.0%
以下、Al;7.0〜20.0%、P;0.015%以下、S;
0.005%以下、Cr;0.5超〜5.5%、さらにTi、Nb
を単独あるいは併用して0.01〜0.5%含有し、残
部鉄および不可避的不純物からなる耐海水鉄筋棒
鋼。
[Claims] 1 C: 1.0% or less, Si: 0.25% or less, Mn: 2.0%
Below, Al; 7.0 to 20.0%, P; 0.015% or less, S;
A seawater-resistant reinforcing steel bar containing 0.005% or less, Cr; more than 0.5 to 5.5%, and the balance consisting of iron and inevitable impurities. 2 C: 1.0% or less, Si: 0.25% or less, Mn: 2.0%
Below, Al; 7.0 to 20.0%, P; 0.015% or less, S;
0.005% or less, Cr; more than 0.5 to 5.5%, plus Ti, Nb
A seawater-resistant reinforcing steel bar containing 0.01 to 0.5% of either alone or in combination, with the balance consisting of iron and unavoidable impurities.
JP11754086A 1986-02-25 1986-05-23 Reinforcing bar having resistance to salt-water corrosion Granted JPS62274050A (en)

Priority Applications (5)

Application Number Priority Date Filing Date Title
JP11754086A JPS62274050A (en) 1986-05-23 1986-05-23 Reinforcing bar having resistance to salt-water corrosion
CA000529832A CA1292135C (en) 1986-02-25 1987-02-16 Concrete reinforcing steel bar or wire
AU68865/87A AU568260B2 (en) 1986-02-25 1987-02-17 Anti-corrosion concrete reinforcing aluminium-steel
GB8704153A GB2186886B (en) 1986-02-25 1987-02-23 Steel composition
US07/148,138 US4836981A (en) 1986-02-25 1988-01-25 Concrete reinforcing steel bar or wire

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP11754086A JPS62274050A (en) 1986-05-23 1986-05-23 Reinforcing bar having resistance to salt-water corrosion

Publications (2)

Publication Number Publication Date
JPS62274050A JPS62274050A (en) 1987-11-28
JPH0430464B2 true JPH0430464B2 (en) 1992-05-21

Family

ID=14714323

Family Applications (1)

Application Number Title Priority Date Filing Date
JP11754086A Granted JPS62274050A (en) 1986-02-25 1986-05-23 Reinforcing bar having resistance to salt-water corrosion

Country Status (1)

Country Link
JP (1) JPS62274050A (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100466497B1 (en) * 2000-12-21 2005-01-13 주식회사 포스코 Device for manufact uring the hot strip with high seaside corrosion resistance

Also Published As

Publication number Publication date
JPS62274050A (en) 1987-11-28

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