JPH0341527B2 - - Google Patents

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Publication number
JPH0341527B2
JPH0341527B2 JP4895582A JP4895582A JPH0341527B2 JP H0341527 B2 JPH0341527 B2 JP H0341527B2 JP 4895582 A JP4895582 A JP 4895582A JP 4895582 A JP4895582 A JP 4895582A JP H0341527 B2 JPH0341527 B2 JP H0341527B2
Authority
JP
Japan
Prior art keywords
scale
parts
alkaline earth
coating
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
JP4895582A
Other languages
Japanese (ja)
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JPS58167720A (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
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Priority to JP4895582A priority Critical patent/JPS58167720A/en
Publication of JPS58167720A publication Critical patent/JPS58167720A/en
Publication of JPH0341527B2 publication Critical patent/JPH0341527B2/ja
Granted legal-status Critical Current

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Classifications

    • CCHEMISTRY; METALLURGY
    • C21METALLURGY OF IRON
    • C21DMODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
    • C21D1/00General methods or devices for heat treatment, e.g. annealing, hardening, quenching or tempering
    • C21D1/68Temporary coatings or embedding materials applied before or during heat treatment

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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)
  • Preventing Corrosion Or Incrustation Of Metals (AREA)
  • Adhesives Or Adhesive Processes (AREA)

Description

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

本発明は熱延鋼帯や型、条、線材等の鋼材に関
し、その熱間圧延において用いられるスケール防
止剤に係るものである。 周知の通り、鋼材の熱間圧延工程において鋼材
表面にスケールが発生し、鋼材歩留りを低下せし
めるほか、該二次スケールは酸洗性が悪いため生
産性を低下せしめる欠点があり、前記課題を解決
するため、たとえば仕上圧延を出たのち、捲取機
前迄にスケール防止剤を塗布し、二次スケールの
発生を抑止しようとする試みが開示されている。 前記周知のスケール防止剤としては、アルカリ
金属、アルカリ土類金属、ホウ素、アルミニウ
ム、マンガン等の化合物の1種以上からなるもの
や、アルカリ土類金属(たとえばカルシウム、マ
グネシウム等)の酸化物、炭酸塩、水酸化物から
なるものが提案されている。それらスケール防止
剤は水に混合され、スプレイ塗布されるかロール
塗布される手段が採用されており、均一塗布の目
的のため分散剤が添加される場合もあつた。 ところで周知のスケール防止剤は、一応の効果
は認められるものの、鋼材に対する付着性に問題
があるほか、コストや後処理問題で経済性が低い
などの未解決の技術的課題が残され、広く使用さ
れるに至つていないのが現状である。 そこで本発明者等は、接着性が良くかつスケー
ル防止効果が高く、後処理の容易なスケール防止
剤の開発を行ない本発明を完成した。 本発明の要旨はNa2O・3SiO2からなる接着剤
を、アルカリ土類金属化合物100部に対し1〜30
部配合し、水を加えてスラリー状とした鋼材の熱
間圧延スケール防止剤であつて、以下本発明につ
いてさらに詳細に説明する。 本発明の特徴は低融点物質即ちNa2O・3SiO2
(融点600℃)を接着剤として用いる点にある。そ
の理由は高温度を保持したまま、高速で移送され
ている鋼材表面に、周知のスケール防止剤をスプ
レーするかあるいはラミナーフローさせても瞬間
的に蒸気膜が生じ、水滴となつて表面にころがり
付着し難いと云う技術的課題を解決する点にあ
り、即ち本発明にかかる前記接着剤を適量用いる
と、スケール防止剤の濃度が向上し、付着力が著
しく高まり、塗布効率が改善される。 次に本発明においてアルカリ土類金属化合物と
しては、Ca,Mg等の酸化物、水酸化物、炭酸
塩、リン酸塩の1種又は2種以上を用いるが、ア
ルミニウム粉末(融点約660℃)、ガラス粉末例え
ば軟化点が約500〜700℃の硅酸ソーダガラスのい
ずれかまたは双方を1〜10%添加もしくは酸化ホ
ウ素(B2O3、融点約450℃以上)を5%以下の割
合で添加してもよい。 この理由はアルミニウム粉末、ガラス粉末、酸
化ホウ素等は、アルカリ土類金属化合物例えば炭
酸カルシウム(CaCO3、分解温度898℃)が分解
するまでの間に鋼材の表面で溶融し、アルカリ土
類金属化合物の付着性を高め鋼材の酸化を抑制、
または改質を向上するための添加剤としての作用
を有するためで、アルミニウム粉末、ガラス粉末
の添加量が1%未満では効果がなく、また10%超
ではアルカリ土類金属化合物の効果を減少させる
と共に、塗布性を低下させ、一方、酸化ホウ素も
同様に添加量が1%未満では効果がなく、5%超
では効果が減少し、塗布性を低下させるため前述
の添加量の範囲が望ましい。さらにアルカリ土類
金属化合物100部に対し、前記接着剤を1〜30部
配合するが、その配合比率の限定理由は次の通り
である。 前記接着剤は、高温度の鋼材に接触すると400
〜1100℃で溶融、展着しアルカリ土類金属化合物
の粉状体を鋼材に付着させるもので、低融点の無
機系物質が接着剤として最適である。 前記接着剤はアルカリ土類金属化合物100部に
対し、1部未満ではアルカリ土類金属化合物を展
着するのに不充分で最底で1部以上は必要であ
る。 一方前記接着剤が30部超になると、鋼材とアル
カリ土類金属化合物との接触が少なくなり、二次
スケールの防止が不充分になる。ここで二次スケ
ールの防止とはスケール厚みを薄くすることであ
るが、硫酸酸洗性及び剥離性に悪いFe3O4を少く
し、それらに良好なFeOを多くすることも含むも
のである。 また、塗布前のスケール防止剤が水溶液中で沈
降しにくい様にするため、少量の分散剤を添加し
ても良い。 次に前記アルカリ土類金属化合物と接着剤の混
合物に水を加えてスラリー状とするが、その比は
水100部に対し混合物1〜100部とする。その理由
は次の通りである。 水100部に対し、混合物が1部未満ではスケー
ル防止効果及び塗布鋼材の酸洗時間の短縮に効果
がなく、酸性ピロリン酸カルシウムでは1部超で
効果を現わす。一方100部超では前記スラリー状
物体の粘度が高くなり、スプレイ塗布がしにくく
なると、スプレイ圧力を高くせねばならなくなる
ため、鋼材に前記スラリー状物体を吹付けた際、
はねかえりが多くなつて塗布効率が低下するの
で、混合物の配合割合は水100部に対し、1〜100
部が適当である。スプレイ法の場合、ノズルは径
が20mm以上のものがノズル詰りが少なくて良い
し、かつ長距離まで塗布可能なノズルが塗布効率
の面でも望ましい。 本発明のスケール防止剤の塗布は次の如く実施
する。 (1) 加熱炉直後に設置された高圧水デスケーリン
グのあと、又は粗圧延後仕上圧延出側までの途
中で鋼材表面にスプレー法により塗布する。塗
布量は仕上圧延後の塗布に比べ3〜20倍位多目
が良い。これは塗布後の熱延による延伸と、鋼
材温度が高いため熱対流の影響を小さくするた
めである。吐出圧は1〜10Kg/cm2(気水噴霧ノ
ズルの場合は空気圧を1〜6Kg/cm2)が良い。
吐出圧が大き過ぎるとスケール防止剤が鋼材に
ぶつかつた後はね返るので良くない。 (2) 仕上圧延中のロールスタンドにおいて、ロー
ルを用いて鋼材表面にロールコーテイングする
かもしくはスプレイする。 つまりスケール防止剤をバツクアツプロール
に展着するか、鋼材とワークロール間又はワー
クロールにスプレイ塗布して鋼材表面に付着さ
せる。スプレイ塗布の場合は、1〜6Kg/cm2
吐出圧(流体の場合空気圧は1〜5Kg/cm2)が
良い。吐出量(又は付着量)は仕上圧延後塗布
の1〜10倍必要である。 (3) 仕上圧延出側で最終スタンドを出た直後の鋼
材表面にスプレー法により塗布する。吐出圧は
1〜6Kg/cm2が良く、低すぎるとスケール防止
剤が鋼材に到達せず、高過ぎると反撥してしま
う。1個当りの吐出量が1〜10Kg/mmのノズル
を巾方向及び長手方向に数10個並べてスケール
防止剤の鋼板上への付着量が適正な値になる様
にする。 第1図に示す様に炭酸カルシウム塗布した場
合、酸化カルシウム量で30mg/m2(片面)付着
していると硫酸酸洗時間が半減する。さらに塗
布距離は50〜150cmが良い。近過ぎると鋼材が
仕上圧延機を出た後ジヤンプしたり、曲つたり
してノズルにぶつかる可能性があり、遠すぎる
とスケール防止剤が鋼材まで到達せず熱対流で
飛散して鋼材に付着しないことがある。 (4) 仕上圧延され、捲取機にて捲取られる直前及
び捲取後の鋼材表面にスプレー法によつて塗布
する。塗布条件は前記(3)の条件と同じで良い
が、捲取後の場合捲取つた鋼帯の側面から塗布
し、鋼帯両端部のみ塗布できれば良い。一般に
熱延鋼帯の両端部は、巾中央部に比べ酸洗時間
が長いので、両端部のみ塗布できる巾方向に移
動調整可能なスプレイ装置を熱延ラインに設置
し、塗布せしめるのも効果的である。 本発明のスケール防止剤を塗布して、前述の(1)
〜(4)迄の処理を施した場合、圧延や環境に何等の
問題も生ずることなく、二次スケールの改質又は
発生量は減少し、酸洗時間が半減する。この理由
は酸洗ラインのロール等による曲げ加工により、
二次スケールに多数の亀裂が発生し、塩酸もしく
は硫酸酸洗が効果的に機能するため、大巾に時間
が短縮されるものと認められる。 さらに酸洗終了後、製品化された鋼材に発生す
る二次スケールの剥離性も極めて良好である。 次に本発明を実施例に従つて説明する。 実施例 1 連続鋳造された12トンの低炭素鋼スラブを加熱
炉で1250℃に加熱し、抽出、高圧水デスケーリン
グ後粗圧延、仕上圧延直後で、スケール防止剤を
吐出圧2〜4Kg/cm2、空気圧2〜3Kg/cm2、塗布
距離45〜100cmでスプレイ塗布し、その後ホツト
ランテーブルで注水又は無注水後、2mm厚の鋼帯
をコイル状に捲取つた。捲戻し後、コイル頭部中
央部及び尾部から試験材を採取し、90℃の15%硫
酸液で酸洗した。本発明の防止剤は付着効率がき
わめて高く、酸洗時間も大巾に短縮できる。又曲
げによりスケール剥離性も良好である。 第1表にスケール防止剤の組成、塗布条件、塗
布および酸洗結果を示す。
The present invention relates to steel materials such as hot-rolled steel strips, molds, strips, and wire rods, and relates to a scale inhibitor used in hot rolling thereof. As is well known, scale is generated on the surface of the steel material during the hot rolling process of steel material, which reduces the yield of steel material.In addition, secondary scale has the drawback of reducing productivity due to poor pickling properties.This problem has been solved. In order to prevent this, for example, an attempt has been made in which an anti-scaling agent is applied after the finish rolling to the front of the winding machine to suppress the generation of secondary scale. The well-known scale inhibitors include those consisting of one or more compounds of alkali metals, alkaline earth metals, boron, aluminum, manganese, etc., oxides of alkaline earth metals (for example, calcium, magnesium, etc.), and carbonic acid. Those consisting of salts and hydroxides have been proposed. These scale inhibitors are mixed with water and spray coated or roll coated, and sometimes a dispersant is added for the purpose of uniform coating. By the way, although well-known scale inhibitors are somewhat effective, they still have unresolved technical issues such as problems with adhesion to steel materials and low economic efficiency due to cost and post-treatment issues, so they are not widely used. The current situation is that this has not yet been achieved. Therefore, the present inventors developed a scale inhibitor that has good adhesive properties, a high scale prevention effect, and is easy to post-process, and completed the present invention. The gist of the present invention is to use an adhesive consisting of Na 2 O.3SiO 2 in an amount of 1 to 30 parts per 100 parts of an alkaline earth metal compound.
The present invention is a hot rolling scale inhibitor for steel materials which is prepared into a slurry by adding water to the hot rolling scale inhibitor. The feature of the present invention is that low melting point substances, namely Na 2 O・3SiO 2
(melting point 600℃) is used as an adhesive. The reason for this is that even if a well-known anti-scaling agent is sprayed or laminar flow is applied to the surface of a steel material that is being transported at high speed while maintaining a high temperature, a vapor film is instantaneously formed and water droplets roll onto the surface. The purpose is to solve the technical problem of difficulty in adhesion, that is, when the adhesive according to the present invention is used in an appropriate amount, the concentration of the scale inhibitor is increased, the adhesion force is significantly increased, and the coating efficiency is improved. Next, in the present invention, as the alkaline earth metal compound, one or more of oxides, hydroxides, carbonates, and phosphates of Ca, Mg, etc. are used, and aluminum powder (melting point: about 660°C) , glass powder, such as sodium silicate glass with a softening point of about 500 to 700°C, or both, at a rate of 1 to 10%, or boron oxide (B 2 O 3 , melting point of about 450°C or higher) at a rate of 5% or less. May be added. The reason for this is that aluminum powder, glass powder, boron oxide, etc. melt on the surface of the steel material until alkaline earth metal compounds such as calcium carbonate (CaCO 3 , decomposition temperature 898°C) decompose, and the alkaline earth metal compounds improves adhesion and suppresses oxidation of steel materials,
Or, it acts as an additive to improve modification, and if the amount of aluminum powder or glass powder added is less than 1%, it will not be effective, and if it exceeds 10%, it will reduce the effect of the alkaline earth metal compound. On the other hand, boron oxide has no effect if the amount added is less than 1%, and if it exceeds 5%, the effect decreases and reduces the coating property, so the above-mentioned range of addition amount is desirable. Furthermore, 1 to 30 parts of the adhesive is added to 100 parts of the alkaline earth metal compound, and the reasons for limiting the mixing ratio are as follows. 400°C when the adhesive comes in contact with high temperature steel.
It melts and spreads at ~1100°C to attach powdered alkaline earth metal compounds to steel materials, and inorganic materials with low melting points are ideal as adhesives. If the amount of the adhesive is less than 1 part per 100 parts of the alkaline earth metal compound, it will be insufficient to spread the alkaline earth metal compound, and at least 1 part is required at the bottom. On the other hand, if the amount of the adhesive exceeds 30 parts, the contact between the steel material and the alkaline earth metal compound will be reduced, and the prevention of secondary scale will be insufficient. Here, prevention of secondary scale means reducing the thickness of the scale, but it also includes reducing Fe 3 O 4 , which is bad for sulfuric acid pickling properties and peelability, and increasing FeO, which is good for them. Further, a small amount of a dispersant may be added to prevent the scale preventive agent from settling in the aqueous solution before coating. Next, water is added to the mixture of the alkaline earth metal compound and adhesive to form a slurry, and the ratio is 1 to 100 parts of the mixture to 100 parts of water. The reason is as follows. If the mixture is less than 1 part per 100 parts of water, it will not be effective in preventing scale or shortening the pickling time of coated steel materials, but with acidic calcium pyrophosphate, if it is more than 1 part, it will be effective. On the other hand, if the amount exceeds 100 parts, the viscosity of the slurry-like substance becomes high and spray application becomes difficult, and the spray pressure must be increased.
Since splashing increases and coating efficiency decreases, the proportion of the mixture should be 1 to 100 parts per 100 parts of water.
section is appropriate. In the case of the spray method, a nozzle with a diameter of 20 mm or more is preferable because it reduces nozzle clogging, and a nozzle that can coat over long distances is desirable in terms of coating efficiency. Application of the scale inhibitor of the present invention is carried out as follows. (1) Apply by spraying to the steel surface after high-pressure water descaling installed immediately after the heating furnace, or after rough rolling and on the way to the finish rolling exit side. The amount of coating should be about 3 to 20 times higher than the coating after finish rolling. This is to reduce the effects of hot rolling after coating and thermal convection due to the high temperature of the steel material. The discharge pressure is preferably 1 to 10 kg/cm 2 (in the case of an air/water spray nozzle, the air pressure is 1 to 6 kg/cm 2 ).
If the discharge pressure is too high, the anti-scaling agent will rebound after hitting the steel material, which is not good. (2) Roll coating or spraying is applied to the surface of the steel using rolls on a roll stand during finish rolling. That is, the anti-scaling agent is spread on the back-up roll, or it is spray-coated between the steel material and the work roll or onto the work roll so that it adheres to the surface of the steel material. In the case of spray coating, a discharge pressure of 1 to 6 kg/cm 2 (in the case of fluid, the air pressure is 1 to 5 kg/cm 2 ) is preferable. The discharge amount (or coating amount) is required to be 1 to 10 times the amount applied after finishing rolling. (3) Apply by spraying to the surface of the steel material immediately after leaving the final stand on the finish rolling exit side. The discharge pressure is preferably 1 to 6 kg/ cm2 ; if it is too low, the scale inhibitor will not reach the steel material, and if it is too high, it will be repelled. Several tens of nozzles with a discharge rate of 1 to 10 kg/mm per nozzle are arranged in the width and length directions so that the amount of scale preventive agent deposited on the steel plate becomes an appropriate value. When calcium carbonate is applied as shown in Figure 1, if the calcium oxide amount is 30 mg/m 2 (one side), the sulfuric acid pickling time is halved. Furthermore, the coating distance is preferably 50 to 150 cm. If it is too close, the steel material may jump or bend after leaving the finishing mill and hit the nozzle; if it is too far away, the scale preventive agent will not reach the steel material and will be scattered by thermal convection and adhere to the steel material. There are things I don't do. (4) Apply by spraying to the surface of the finished steel material just before and after being rolled up in a winding machine. The coating conditions may be the same as those in (3) above, but after winding, it is sufficient to apply from the side of the rolled steel strip and apply only to both ends of the steel strip. In general, pickling time is longer at both ends of a hot-rolled steel strip than at the center of the width, so it is also effective to install a spray device on the hot-rolling line that can be adjusted to move in the width direction so that only both ends can be coated. It is. Applying the scale inhibitor of the present invention, the above-mentioned (1)
When the treatments from (4) to (4) are performed, no problems occur in rolling or the environment, the amount of secondary scale modification or generation is reduced, and the pickling time is halved. The reason for this is that due to the bending process using rolls in the pickling line,
It is recognized that many cracks occur in the secondary scale and that the hydrochloric acid or sulfuric acid pickling works effectively, resulting in a significant reduction in time. Furthermore, after pickling, the peelability of secondary scale that occurs on the manufactured steel material is also extremely good. Next, the present invention will be explained according to examples. Example 1 A continuously cast 12 ton low carbon steel slab was heated to 1250°C in a heating furnace, extracted, and immediately after high-pressure water descaling, rough rolling, and finishing rolling, a scale inhibitor was applied at a discharge pressure of 2 to 4 kg/cm. 2. Spray coating was carried out at an air pressure of 2 to 3 kg/cm 2 and a coating distance of 45 to 100 cm, and then a 2 mm thick steel strip was wound into a coil after water was poured on a hot run table or after water was not poured. After unwinding, test materials were taken from the center and tail of the coil head and pickled with a 15% sulfuric acid solution at 90°C. The inhibitor of the present invention has extremely high adhesion efficiency and can greatly shorten pickling time. Furthermore, the scale removability is also good upon bending. Table 1 shows the composition of the scale inhibitor, coating conditions, coating and pickling results.

【表】【table】

【表】 実施例 2 上記実施例1と同様の方法で、捲取直前でスケ
ール防止剤として酸性ピロリン酸カルシユウム20
%、ケイ酸ソーダ2%、水78%水溶液を塗布し、
試験材を採取後2次スケール性状を調査した。 第2表に示す通り、本発明のスケール防止材を
用いた場合、スケール厚みが従来材(無塗布)に
比べ約1/3、塩酸々洗時間は約1/2に短縮した。ま
た本発明の防止剤は酸性ピロリン酸カルシウムの
単独水溶液に比べて、塗布効率5〜10倍向上し
た。
[Table] Example 2 In the same manner as in Example 1 above, acidic calcium pyrophosphate 20 was added as a scale inhibitor just before winding.
%, sodium silicate 2%, water 78% aqueous solution,
After collecting the test material, the secondary scale properties were investigated. As shown in Table 2, when the scale preventive material of the present invention was used, the scale thickness was reduced to about 1/3 compared to the conventional material (uncoated), and the hydrochloric acid cleaning time was reduced to about 1/2. Furthermore, the coating efficiency of the inhibitor of the present invention was 5 to 10 times higher than that of a single aqueous solution of calcium acid pyrophosphate.

【表】【table】 【図面の簡単な説明】[Brief explanation of drawings]

第1図はCaO付着量と硫酸々洗時間との関係を
示すグラフである。
FIG. 1 is a graph showing the relationship between the amount of CaO deposited and the washing time with sulfuric acid.

Claims (1)

【特許請求の範囲】 1 Na2O・3SiO2からなる接着剤を、アルカリ
土類金属化合物100部に対し、1〜30部配合し、
水を加えてスラリー状とした鋼材の熱間圧延スケ
ール防止剤。 2 Na2O・3SiO2からなる接着剤に、1〜10%
のAl粉末又はガラス粉末のいずれか、もしくは
1〜5%のB2O3を添加してなる接着剤を、アル
カリ土類金属化合物100部に対し、1〜30部配合
し、水を加えてスラリー状とした鋼材の熱間圧延
スケール防止剤。
[Claims] 1. 1 to 30 parts of an adhesive consisting of Na 2 O.3SiO 2 is blended to 100 parts of an alkaline earth metal compound,
A hot rolling scale inhibitor for steel materials made into a slurry by adding water. 2 1 to 10% to the adhesive consisting of Na 2 O and 3SiO 2
Mix 1 to 30 parts of an adhesive made of either Al powder or glass powder, or 1 to 5% B 2 O 3 to 100 parts of an alkaline earth metal compound, and add water. A hot rolling scale inhibitor for steel materials in slurry form.
JP4895582A 1982-03-29 1982-03-29 Descaling agent for steel material to be hot-rolled Granted JPS58167720A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP4895582A JPS58167720A (en) 1982-03-29 1982-03-29 Descaling agent for steel material to be hot-rolled

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP4895582A JPS58167720A (en) 1982-03-29 1982-03-29 Descaling agent for steel material to be hot-rolled

Publications (2)

Publication Number Publication Date
JPS58167720A JPS58167720A (en) 1983-10-04
JPH0341527B2 true JPH0341527B2 (en) 1991-06-24

Family

ID=12817694

Family Applications (1)

Application Number Title Priority Date Filing Date
JP4895582A Granted JPS58167720A (en) 1982-03-29 1982-03-29 Descaling agent for steel material to be hot-rolled

Country Status (1)

Country Link
JP (1) JPS58167720A (en)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH03162516A (en) * 1989-11-20 1991-07-12 Kawasaki Steel Corp Continuous annealing method for stainless steel strip
JPH0753916B2 (en) * 1990-03-19 1995-06-07 住友金属工業株式会社 Oily scale inhibitor for hot rolling and hot rolling method
CN1229298C (en) * 1999-01-27 2005-11-30 金伟华 Inorganic binder employing waste glass

Also Published As

Publication number Publication date
JPS58167720A (en) 1983-10-04

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