JPH11293500A - Surface flaw removal method for hot rolled steel strip - Google Patents
Surface flaw removal method for hot rolled steel stripInfo
- Publication number
- JPH11293500A JPH11293500A JP10095972A JP9597298A JPH11293500A JP H11293500 A JPH11293500 A JP H11293500A JP 10095972 A JP10095972 A JP 10095972A JP 9597298 A JP9597298 A JP 9597298A JP H11293500 A JPH11293500 A JP H11293500A
- Authority
- JP
- Japan
- Prior art keywords
- steel strip
- electrolysis
- rolled steel
- hot
- chloride
- 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.)
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Landscapes
- Cleaning And De-Greasing Of Metallic Materials By Chemical Methods (AREA)
Abstract
(57)【要約】
【課題】熱延鋼帯の表面疵を酸類を使用しないで除去
し、歩留まりを改善すると共に、製品の商品価値を高め
る。
【解決手段】熱延鋼帯を脱スケールした後、溶媒が水で
溶質の主成分が塩化物である電解液中で陽極電解する熱
延鋼帯の表面疵除去方法。
(57) [Summary] [PROBLEMS] To remove the surface flaw of a hot-rolled steel strip without using acids, improve the yield, and increase the commercial value of the product. A method for removing surface flaws of a hot-rolled steel strip, in which after the hot-rolled steel strip is descaled, anodic electrolysis is performed in an electrolyte in which the solvent is water and the solute is mainly a chloride.
Description
【0001】[0001]
【発明の属する技術分野】本発明は熱延鋼帯の表面疵を
陽極電解により除去する方法に関する。The present invention relates to a method for removing surface defects of a hot-rolled steel strip by anodic electrolysis.
【0002】[0002]
【従来の技術】炭素鋼などの熱延鋼帯は、スラブを熱間
圧延することによって製造されるが、熱間圧延時に鋼帯
表面に生成した酸化スケールが圧延ロールによって地金
に押し込まれて、表面疵になることがある。表面疵は、
熱間圧延後の鋼帯を酸洗して酸化スケールを除去するこ
とによって顕在化するので、酸化スケールが付着した状
態では疵の有無は判別できない。2. Description of the Related Art Hot-rolled steel strips such as carbon steel are produced by hot-rolling slabs. Oxidized scale formed on the steel strip surface during hot rolling is pressed into the base metal by rolling rolls. , May cause surface flaws. Surface flaws
Since the steel strip after hot rolling is exposed by pickling the steel strip to remove oxide scale, the presence or absence of a flaw cannot be determined in a state where the oxide scale is attached.
【0003】酸洗は、鋼帯表面の酸化スケールを除去す
る(脱スケールする)目的で行われるので、通常は酸洗
液にスケールのみが溶解し地金が溶解しないように、イ
ンヒビターを添加した酸洗液が用いられる。そのため、
熱間圧延で表面疵が発生した鋼帯は酸洗後も疵のある表
面となり、製品の商品価値を著しく低下させる。また、
特に表面疵の多い鋼帯は実際には商品として販売するこ
とができないのでスクラップとして処理せざるを得な
い。その結果、製造コストを高騰させることになる。Since pickling is performed for the purpose of removing (descaling) oxide scale on the surface of a steel strip, an inhibitor is usually added to the pickling solution so that only the scale is dissolved and the metal is not dissolved. An acid pickling solution is used. for that reason,
A steel strip having surface flaws generated by hot rolling has a flawed surface even after pickling, which significantly reduces the commercial value of the product. Also,
In particular, a steel strip having many surface flaws cannot be sold as a commercial product, and must be treated as scrap. As a result, manufacturing costs will increase.
【0004】鋼帯の一般的な脱スケール方法としては、
10%程度の塩酸に浸漬する方法があるが、最近は電解
処理による脱スケール方法も検討されている。[0004] As a general method of descaling a steel strip,
There is a method of immersion in about 10% hydrochloric acid, but recently, a descaling method by electrolytic treatment is also being studied.
【0005】例えば、日本鉄鋼協会が編集した鉄と鋼、
第67巻(1981年発行)のS393およびS394
ページには、塩化ナトリウムあるいは硫酸ナトリウム水
溶液中で電解する鋼線の脱スケール方法が開示されてい
る。For example, iron and steel edited by the Iron and Steel Institute of Japan,
S393 and S394 in Volume 67 (issued in 1981)
The page discloses a method for descaling steel wires electrolyzed in aqueous sodium chloride or sodium sulfate solutions.
【0006】また、同じく日本鉄鋼協会が編集した材料
とプロセス、第7巻(1994年発行)の1428ペー
ジには、希塩酸水溶液中で電解する熱間圧延鋼鈑の脱ス
ケール方法が開示されている。[0006] Materials and Processes, also edited by the Iron and Steel Institute of Japan, Vol. 7 (published in 1994), page 1428, discloses a method for descaling hot rolled steel sheets electrolyzed in dilute hydrochloric acid aqueous solution. .
【0007】特開昭57−161097号公報には、酸
性の塩化物水溶液中で電解する鋼線の脱スケール方法が
開示されている。JP-A-57-161097 discloses a method of descaling a steel wire which is electrolyzed in an acidic chloride aqueous solution.
【0008】しかし、これらの方法はいずれも鋼材表面
のスケールを効率よく除去することを目的とするもので
あり、脱スケール後の鋼帯の表面疵の除去には役立たな
い。However, all of these methods aim at efficiently removing the scale on the surface of the steel material, and are not useful for removing the surface defects of the steel strip after the descaling.
【0009】[0009]
【発明が解決しようとする課題】本発明の課題は、人体
や環境に有害で、危険性の高い酸類を使用しないで、熱
延鋼帯の表面疵を除去することにより歩留まり(直行
率)を高め、製造コストを低減すると共に、製品の商品
価値を高めることができる表面疵の除去方法を提供する
ことにある。SUMMARY OF THE INVENTION An object of the present invention is to remove the surface flaws of a hot-rolled steel strip without using acids which are harmful to the human body and the environment and have high danger, thereby improving the yield (orthogonality rate). It is an object of the present invention to provide a method for removing surface flaws, which can increase the production cost while increasing the commercial value of a product.
【0010】[0010]
【課題を解決するための手段】熱延鋼帯の表面疵を除去
する方法に係わる本発明の要旨は、以下の通りである。The gist of the present invention relating to a method for removing surface flaws of a hot-rolled steel strip is as follows.
【0011】(1)熱延鋼帯を脱スケールした後、溶媒
が水で溶質の主成分が塩化物である電解液中で陽極電解
することを特徴とする熱延鋼帯の表面疵除去方法。(1) A method for removing surface flaws on a hot-rolled steel strip, which comprises descaling the hot-rolled steel strip, followed by anodic electrolysis in an electrolytic solution in which the solvent is water and the solute is mainly a chloride. .
【0012】(2)負極として金属ニッケルからなる電
極、正極として酸化物を被覆した金属チタンからなる電
極を用いて間接通電法により陽極電解することを特徴と
する請求項1記載の熱延鋼帯の表面疵除去方法。(2) The hot-rolled steel strip according to claim 1, wherein anodic electrolysis is performed by an indirect energization method using an electrode made of nickel metal as a negative electrode and an electrode made of metal titanium coated with an oxide as a positive electrode. Surface flaw removal method.
【0013】本発明者らは、酸洗後の熱延鋼帯の表面疵
を除去する方法について種々検討した結果、塩化物を主
成分とする水溶液中で陽極電解すると熱延鋼帯の地金が
溶解するとの知見を得て本発明を完成させた。The present inventors have conducted various studies on a method of removing surface defects of a hot-rolled steel strip after pickling. As a result, when anodic electrolysis is performed in an aqueous solution containing chloride as a main component, the metal of the hot-rolled steel strip is ingot. The present invention was completed based on the finding that is dissolved.
【0014】[0014]
【発明の実施の形態】以下、本発明の表面疵除去方法に
ついて詳細に説明する。BEST MODE FOR CARRYING OUT THE INVENTION The surface flaw removing method of the present invention will be described below in detail.
【0015】本発明の方法が対象とする熱延鋼帯は、炭
素鋼帯が好適であり、他にクロム等の合金元素を約1質
量%以下を含む低合金鋼(構造用合金鋼等)などの鋼帯
にも適用できる。The hot-rolled steel strip to which the method of the present invention is applied is preferably a carbon steel strip, and a low-alloy steel (including structural alloy steel) containing about 1% by mass or less of an alloying element such as chromium. It can also be applied to such steel strips.
【0016】熱延鋼帯に陽極電解を施すのは、鋼帯表面
を溶解して表面疵を小さくしたり、消失させるためであ
る。陰極電解法では、鋼帯表面を溶解することができな
く、表面疵を除去するのには適していない。The anodic electrolysis is applied to the hot-rolled steel strip in order to melt the surface of the steel strip to reduce or eliminate surface flaws. In the cathodic electrolysis, the steel strip surface cannot be melted, and is not suitable for removing surface flaws.
【0017】また、陽極電解の前に熱延鋼帯に脱スケー
ルを施すのは、スケールが付着した熱延鋼帯に陽極電解
を施しても鋼帯の地金を溶解することができないからで
ある。The descaling of the hot-rolled steel strip before the anodic electrolysis is performed because the ingot of the steel strip cannot be melted even if the anodic electrolysis is applied to the hot-rolled steel strip to which the scale is adhered. is there.
【0018】次に陽極電解について説明する。Next, anodic electrolysis will be described.
【0019】電解液は、溶質としては塩化物を主成分と
する水溶液を用いる。塩化物としては塩化ナトリウムが
推奨されるが、特にこれに限定されるものではなく、塩
化カリウム、塩化マグネシウム、塩化カルシウムなどで
もよい。As the electrolyte, an aqueous solution containing chloride as a main component is used as a solute. As the chloride, sodium chloride is recommended, but is not particularly limited thereto, and may be potassium chloride, magnesium chloride, calcium chloride, or the like.
【0020】水溶液中の塩化物の濃度は特に厳密に管理
する必要はないが、1質量%未満では鋼帯の溶解速度が
小さくなると同時に電気抵抗が大きくなって、電解に伴
う電力ロスが大きくなるので1%以上が望ましい。濃度
が大きいほど鋼帯の溶解速度は大きくなり、電気抵抗は
小さくなるが、飽和濃度以上では過飽和の塩化物が析出
して、鋼帯表面の溶解が不均一になりやすいので、上限
は30質量%程度にするのがよい。なお、塩化物30質
量%とは、塩化物30質量%、水70質量%を意味し、
電解液の濃度は以下同様とする。また、電解液の溶媒、
溶質は全て質量%とする。It is not necessary to strictly control the chloride concentration in the aqueous solution, but if it is less than 1% by mass, the dissolution rate of the steel strip decreases, and at the same time, the electric resistance increases and the power loss accompanying electrolysis increases. Therefore, 1% or more is desirable. The higher the concentration, the higher the dissolution rate of the steel strip and the lower the electrical resistance. However, if the concentration is higher than the saturation concentration, supersaturated chlorides precipitate and the dissolution of the steel strip surface tends to be uneven, so the upper limit is 30 mass%. %. In addition, 30 mass% of chloride means 30 mass% of chloride and 70 mass% of water,
The same applies to the concentration of the electrolyte. Also, the solvent of the electrolytic solution,
All solutes are% by mass.
【0021】塩化物以外に硫酸塩、硝酸塩などの塩類を
1%未満の量で共存させてもよいが、塩化物濃度を高め
るためには、塩化物単味を含む水溶液が望ましい。In addition to chlorides, salts such as sulfates and nitrates may coexist in an amount of less than 1%, but in order to increase the chloride concentration, an aqueous solution containing only chloride is desirable.
【0022】塩化物水溶液のpHは、1未満および10
以上では電極の溶損や劣化が起こりやすいので1〜10
の範囲とするのがよい。なお、pH3以上では電解によ
って溶解した鉄が水酸化物として沈殿し、鋼帯表面に付
着することがあるので、電解後に希塩酸や希硫酸などで
沈殿物を溶解した後、水洗することが望ましい。The pH of the aqueous chloride solution is less than 1 and 10
Above, the electrode is liable to be melted or deteriorated.
It is good to be in the range of. If the pH is 3 or more, iron dissolved by electrolysis may precipitate as hydroxide and adhere to the surface of the steel strip. Therefore, it is desirable to dissolve the precipitate with dilute hydrochloric acid or dilute sulfuric acid after electrolysis and then wash with water.
【0023】塩化物水溶液の温度は、10℃未満では溶
解速度が遅く、塩化物の析出が起こり易い。また、温度
が高いほど溶解速度が速いが、90℃を超えると電解槽
のライニングが劣化しやすくなるので10〜90℃の範
囲とするのが好ましい。When the temperature of the aqueous chloride solution is lower than 10 ° C., the dissolution rate is low, and the precipitation of chloride is likely to occur. The dissolution rate is higher as the temperature is higher, but if it exceeds 90 ° C., the lining of the electrolytic cell is liable to deteriorate.
【0024】図1は、直接通電による陽極電解方法を模
式的に示す図である。直流電源1から通電ロール2を介
して正の電気を鋼帯4に給電しつつ、電解槽5の中の塩
化物水溶液6中の対極(負極)3との間で陽極電解する
方法が推奨される。FIG. 1 is a diagram schematically showing an anodic electrolysis method by direct current supply. A method is recommended in which anodic electrolysis is performed between the counter electrode (negative electrode) 3 in the aqueous chloride solution 6 in the electrolytic cell 5 while supplying positive electricity to the steel strip 4 from the DC power supply 1 via the energizing roll 2. You.
【0025】図2は、間接通電による陽極電解方法を模
式的に示す図である。陽極電解は、通電ロールを使用せ
ず、電解槽5の中の塩化物水溶液6中で間接通電法によ
って電解する方法でもよい。ただし、この場合には鋼帯
が負極3近傍を通過する時のみに陽極電解がおこなわれ
て鋼帯表面が溶解するが、正極7近傍や正極と負極の間
を通過する鋼帯表面は溶解しないので、その分だけ電解
槽を長くする必要がある。FIG. 2 is a diagram schematically showing an anodic electrolysis method by indirect current supply. The anodic electrolysis may be a method in which electrolysis is performed by an indirect energization method in an aqueous chloride solution 6 in an electrolysis tank 5 without using an energizing roll. However, in this case, the anodic electrolysis is performed only when the steel strip passes near the negative electrode 3 to dissolve the steel strip surface, but the steel strip surface passing near the positive electrode 7 or between the positive electrode and the negative electrode does not dissolve. Therefore, it is necessary to lengthen the electrolytic cell accordingly.
【0026】電解時の電流密度は鋼帯表面の溶解速度に
大きな影響を及ぼし、電流密度が大きいほど溶解速度が
大きくなる。その値が20A/m2未満では溶解速度が
小さいため、疵除去に比較的長時間を要し、10000
A/m2を超えると塩素ガスの発生が著しくなるので、
電流密度としては20〜10000A/m2程度が推奨
されるが、必ずしもこれに限定されるものではない。The current density during electrolysis has a great influence on the dissolution rate on the steel strip surface, and the higher the current density, the higher the dissolution rate. When the value is less than 20 A / m 2 , the dissolution rate is low, so that it takes a relatively long time to remove flaws, and
If it exceeds A / m 2 , the generation of chlorine gas becomes remarkable.
A current density of about 20 to 10000 A / m 2 is recommended, but is not necessarily limited to this.
【0027】塩化物水溶液中で使用する負電極としては
金属ニッケル製電極が推奨される。金属ニッケルは、塩
化物水溶液中での陰極電解による溶製損がほとんどな
く、電解しない時でも腐食し難いからである。As the negative electrode used in the aqueous chloride solution, an electrode made of metallic nickel is recommended. This is because metallic nickel has almost no melting loss due to cathodic electrolysis in a chloride aqueous solution and is hardly corroded even when electrolysis is not performed.
【0028】ステンレス鋼や金属チタンも使用できる
が、前者の場合には非電解時に孔食が発生することがあ
るので、数A/m2程度の負電流を流して孔食の発生を
防止するのが望ましい。また、金属チタンを使用する場
合には、塩化物水溶液のpHが3以下であるとチタンの
水素化物が生成して脆化し、電極が破損する恐れがある
ので、pH3以上で使用することが望ましい。Although stainless steel and titanium metal can be used, in the former case, pitting may occur during non-electrolysis, so that a negative current of about several A / m 2 is passed to prevent the occurrence of pitting. It is desirable. In addition, when metal titanium is used, if the pH of the aqueous chloride solution is 3 or less, hydride of titanium is generated and becomes brittle, and the electrode may be damaged. .
【0029】一方、正電極としてはイリジウム等の酸化
物を被覆した金属チタンからなる電極が推奨される。被
覆する酸化物としてはイリジウム以外に白金やオスミウ
ム等の貴金属の酸化物やチタンの酸化物を混合したもの
も使用できる。酸化物は、チタン表面の陽極酸化による
電気抵抗の増大を防止する効果がある。On the other hand, as the positive electrode, an electrode made of metallic titanium coated with an oxide such as iridium is recommended. As the oxide to be coated, a mixture of an oxide of a noble metal such as platinum or osmium or an oxide of titanium other than iridium can be used. The oxide has an effect of preventing an increase in electric resistance due to anodic oxidation of the titanium surface.
【0030】酸洗後に鋼帯の表面疵の程度を検査する方
法としては、鋼帯の通板速度が比較的遅い場合には目視
による判定が適用できるが、通板速度が速い場合や省力
化のためにはCCDカメラや画像処理装置等を応用した
疵検査装置を使用するのが望ましい。電解処理コストを
削減するためには、酸洗後に鋼帯の表面疵の程度を検査
し、その程度に応じて電解条件を制御するのがよい。制
御可能な電解条件は、電解液の濃度、温度および浸漬時
間等であり、これらにより溶解速度を容易に調整するこ
とができる。As a method of inspecting the degree of surface flaws of the steel strip after pickling, visual judgment can be applied when the steel strip passing speed is relatively low. For this purpose, it is desirable to use a flaw inspection device to which a CCD camera or an image processing device is applied. In order to reduce the electrolytic treatment cost, it is preferable to inspect the degree of surface flaws of the steel strip after pickling, and to control the electrolysis conditions according to the degree. The controllable electrolysis conditions include the concentration, temperature, and immersion time of the electrolytic solution, and the dissolution rate can be easily adjusted by these.
【0031】鋼帯表面を溶解する方法として、例えば塩
酸水溶液に浸漬する方法が考えられる。しかし、本発明
の方法による塩化物水溶液中での陽極電解法の方が疵を
除去する効果が大きい。この理由は定かではないが、電
解の場合には電流が鋼帯表面の凹凸の凸部に多く流れて
溶解が進み、表面の平滑化が速やかに起きるためと推測
される。また、溶解速度自体も塩酸水溶液への浸漬処理
に比べてかなり速いので、処理時間を短縮したり処理槽
の長さを短くすることができるという利点もある。本発
明の方法で使用する塩化物は中性塩であるため、塩酸等
の酸類に比べて人体や環境に対する有害性や危険性が低
いだけでなく、廃液処理に要するアルカリ量が少なく、
スラジ発生量も少なくいという長所がある。As a method of dissolving the surface of the steel strip, for example, a method of immersing the steel strip in an aqueous hydrochloric acid solution can be considered. However, anodic electrolysis in an aqueous chloride solution according to the method of the present invention has a greater effect of removing flaws. The reason for this is not clear, but it is presumed that in the case of electrolysis, a large amount of current flows through the convex portions of the irregularities on the surface of the steel strip, so that the dissolution proceeds and the surface is smoothened promptly. Further, since the dissolution rate itself is considerably faster than the immersion treatment in the hydrochloric acid aqueous solution, there is an advantage that the treatment time can be shortened and the length of the treatment tank can be shortened. Since the chloride used in the method of the present invention is a neutral salt, not only is it less harmful or dangerous to the human body or the environment than acids such as hydrochloric acid, the amount of alkali required for waste liquid treatment is small,
There is an advantage that the amount of generated sludge is small.
【0032】[0032]
【実施例】(実施例1)表1に示す化学組成の2種類の
構造用炭素鋼と2種類の構造用低合金鋼の熱延鋼帯(板
厚3〜5mm)から縦100、横150mmの大きさの
試験片を作製した。これらを朝日化学工業(株)製のイン
ヒビター(商品名:イビット)を0.1質量%含む10
質量%塩酸(温度:80℃)に2〜5分間浸漬して完全
に脱スケールした。この段階で試験片の表面疵の程度を
目視で5段階評価した。評価は、1が最も表面疵が多い
ものであり、5が目視では表面疵が全く認められないも
ので、2〜4は1と5の間の表面疵の程度であり、数値
が大きいほど表面疵が少ないことを示す。EXAMPLES Example 1 A hot rolled steel strip (thickness 3-5 mm) of two types of structural carbon steel and two types of low-alloy structural steel having the chemical compositions shown in Table 1 is 100 mm long and 150 mm wide. A test piece having a size of These contain 10% by mass of an inhibitor (trade name: IBIT) manufactured by Asahi Chemical Industry Co., Ltd.
The sample was immersed in a mass% hydrochloric acid (temperature: 80 ° C.) for 2 to 5 minutes to completely descaling. At this stage, the degree of the surface flaw of the test piece was visually evaluated in five steps. In the evaluation, 1 is the one with the most surface flaws, 5 is that no surface flaws are visually observed, 2 to 4 are the degree of surface flaws between 1 and 5, and the larger the numerical value, the higher the surface flaw. Indicates that there are few flaws.
【0033】疵を評価した後、塩化ナトリウム等の塩化
物を含む水溶液中で金属ニッケル板を対極(負極)とし
て陽極電解した。After the flaws were evaluated, anodic electrolysis was performed in an aqueous solution containing a chloride such as sodium chloride, using the metal nickel plate as a counter electrode (negative electrode).
【0034】[0034]
【表1】 [Table 1]
【0035】図3は、用いた実験用の電解装置の模式図
である。電解液6中に直流電源1に接続した上記寸法の
試験片を浸漬し、試験片の両側面に負極として金属ニッ
ケル板8を対面させて電解した。FIG. 3 is a schematic diagram of the experimental electrolysis apparatus used. The test piece having the above dimensions connected to the DC power supply 1 was immersed in the electrolytic solution 6, and electrolysis was performed with the metal nickel plate 8 facing the negative electrode on both sides of the test piece.
【0036】電解液は、表2に示す8種類とした。ま
た、電解条件を表3に示す。Eight types of electrolytes shown in Table 2 were used. Table 3 shows the electrolysis conditions.
【0037】[0037]
【表2】 [Table 2]
【0038】[0038]
【表3】 [Table 3]
【0039】表2、表3に示すように、比較例として
塩化物を含む水溶液中で陰極電解した場合、硫酸塩お
よび硝酸塩水溶液中で電解した場合およびインヒビタ
ーを含まない80℃の10%塩酸に浸漬した場合の表面
疵の程度も調べた。As shown in Tables 2 and 3, as a comparative example, cathodic electrolysis in an aqueous solution containing chloride, electrolysis in an aqueous solution of sulfate and nitrate, and 10% hydrochloric acid at 80 ° C. containing no inhibitor. The degree of surface flaws when immersed was also examined.
【0040】電解した後、試験片を水洗、乾燥し、再び
上記と同じ評価基準で表面疵の程度を目視で5段階評価
した。After the electrolysis, the test pieces were washed with water and dried, and the degree of surface flaws was visually evaluated according to the same evaluation criteria as above in five steps.
【0041】電解による溶解減量および表面疵の程度を
まとめて表2に示した。Table 2 summarizes the dissolution loss due to electrolysis and the degree of surface flaws.
【0042】表2から明らかなように、塩化物を主成分
とする電解液中で陽極電解した本発明例(試験 No.1〜
14)では電解後の表面疵が全く認められなかった。一
方、比較例のうち塩化物の電解液中で陰極電解したもの
(試験 NO.15および16:電流密度が負の値であるこ
とは陰極電解したことを示す)はほとんど鋼帯表面が溶
解しておらず、表面疵の程度も脱スケール後と全く差が
無かった(すなわち、表面疵が全く除去されなかっ
た)。As is clear from Table 2, examples of the present invention in which anodic electrolysis was carried out in an electrolyte containing chloride as a main component (Test Nos. 1 to 4)
In No. 14), no surface flaw was observed after electrolysis. On the other hand, among the comparative examples, those subjected to cathodic electrolysis in a chloride electrolyte (Test Nos. 15 and 16: a negative current density indicates that cathodic electrolysis was performed) almost completely dissolves the steel strip surface. The degree of surface flaws was not different from that after descaling (ie, no surface flaws were removed).
【0043】また、比較例のうち、電解液に塩化物が含
まれていない場合(試験 NO.17〜20)も、表面がほ
とんど溶解しておらず、表面疵は全く除去されなかっ
た。さらに、脱スケール後にインヒビターを含まない8
0℃、10%塩酸に60秒間浸漬した場合(試験 NO.2
1〜24)には、ある程度表面が溶解して表面疵が減少
したが、本発明例には及ばなかった。In the comparative examples, when the electrolyte solution did not contain chloride (Test Nos. 17 to 20), the surface was hardly dissolved, and the surface flaw was not removed at all. In addition, after descaling, no inhibitor
When immersed in 0% and 10% hydrochloric acid for 60 seconds (Test No. 2
In Nos. 1 to 24), the surface was melted to some extent and the surface flaws were reduced, but were not as good as those of the present invention.
【0044】(実施例2)表1に示したAおよびDの鋼
帯より、幅300mmの鋼帯を切り出し、試験用連続酸
洗−電解装置を用いて、脱スケール処理および電解を連
続的におこなった。(Example 2) A steel strip having a width of 300 mm was cut out from the steel strips A and D shown in Table 1, and the descaling treatment and electrolysis were continuously performed using a continuous pickling-electrolysis apparatus for testing. I did it.
【0045】図4は、使用した4種の装置を模式的に示
した側面図である。FIG. 4 is a side view schematically showing the four types of apparatuses used.
【0046】図4(a)は、脱スケール用の塩酸浸漬槽
12の後に塩化物水溶液の電解液を入れた図1のタイプ
の電解槽13(通電ロールと電解液中金属ニッケルから
なる負極を有する)を配置した装置である。FIG. 4 (a) shows an electrolytic cell 13 of the type shown in FIG. 1 in which an aqueous solution of a chloride aqueous solution is placed after a hydrochloric acid immersion cell 12 for descaling (a negative electrode made of a current-carrying roll and metallic nickel in the electrolytic solution). ) Is disposed.
【0047】図4(b)は、脱スケール用の塩酸浸漬槽
12の後に塩化物水溶液の電解液を入れた図2のタイプ
の電解槽14(電解液中に酸化イリジウム被覆金属チタ
ンからなる正極と金属ニッケル製負極を有する)を配置
した装置である。FIG. 4 (b) shows an electrolytic cell 14 of the type shown in FIG. 2 in which an electrolytic solution of a chloride aqueous solution is placed after a hydrochloric acid immersion tank 12 for descaling (a positive electrode made of iridium oxide-coated metal titanium in the electrolytic solution). And a metal nickel negative electrode).
【0048】図4(c)は、脱スケール用の塩酸浸漬槽
12の後に表面疵除去のための塩酸浸漬槽15を配置し
た装置である。FIG. 4C shows an apparatus in which a hydrochloric acid immersion tank 15 for removing surface flaws is arranged after a hydrochloric acid immersion tank 12 for descaling.
【0049】図4(d)は、脱スケール用の塩酸浸漬槽
12の後に表面疵除去のための処理槽を配置しない装置
である。FIG. 4D shows an apparatus in which a treatment tank for removing surface flaws is not disposed after the hydrochloric acid immersion tank 12 for descaling.
【0050】図4(a)〜図4(c)に示した装置は、
脱スケールの後および電解の後に水洗用のスプレー16
が設けられている。各装置とも、コイル18が巻戻さ
れ、鋼帯11が各処理槽内を連続的に通過し、巻取られ
てコイル19となる。The device shown in FIGS. 4 (a) to 4 (c)
Spray 16 for washing after descaling and after electrolysis
Is provided. In each device, the coil 18 is unwound, and the steel strip 11 continuously passes through each processing tank, and is wound up to form the coil 19.
【0051】脱スケール条件、脱スケール後の電解条件
および処理後の表面疵の程度を表4にまとめて示す。な
お、表面疵の評価基準は表2の場合と同じである。Table 4 summarizes the descaling conditions, the electrolysis conditions after descaling, and the degree of surface flaws after the treatment. The evaluation criteria for surface flaws are the same as those in Table 2.
【0052】[0052]
【表4】 [Table 4]
【0053】試験 NO.1および2は、図4(a)のタイ
プの装置を用いた場合であり、疵除去用電解槽の長さが
約3m、電解がおこなわれる正味長さは1.5mであ
る。従って、通板速度が4.5m/minの場合は20
秒間、1.5m/minの場合は60秒間の陽極電解が
おこなわれる。また、電解の総電流が900A、電解面
積が0.45m2なので、電流密度は2000A/m2と
なる。Tests Nos. 1 and 2 were conducted using an apparatus of the type shown in FIG. 4 (a). The length of the electrolytic cell for flaw removal was about 3 m, and the net length at which electrolysis was performed was 1.5 m. It is. Therefore, when the passing speed is 4.5 m / min, 20
In the case of 1.5 m / min, anodic electrolysis is performed for 60 seconds. Since the total current of the electrolysis is 900 A and the electrolysis area is 0.45 m 2 , the current density is 2000 A / m 2 .
【0054】試験 NO.3および4は、図4(b)のタイ
プの装置を用いた場合であり、疵除去用電解槽の長さが
約5m、陽極電解が行われる正味長さは1.5mなの
で、試験NO.1および2の場合と同じく通板速度が4.
5m/minの場合は20秒間、1.5m/minの場
合は60秒間の陽極電解 (電流密度:2000A/
m2)がおこなわれる。Tests Nos. 3 and 4 were conducted using an apparatus of the type shown in FIG. 4B. The length of the electrolytic cell for flaw removal was about 5 m, and the net length for anodic electrolysis was 1. 5 m, so that the passing speed is 4. as in Test Nos. 1 and 2.
Anode electrolysis for 20 seconds at 5 m / min and 60 seconds at 1.5 m / min (current density: 2000 A /
m 2 ) is performed.
【0055】試験NO.5および6は、図4(c)のタイプ
の装置を用いた場合であり、疵除去用浸漬槽の長さが約
5m、正味浸漬長さが4.5mなので、通板速度が4.
5m/minの場合は60秒間、1.5m/minの場
合は180秒間の浸漬処理がおこなわれる。Tests Nos. 5 and 6 were conducted using an apparatus of the type shown in FIG. 4C. The length of the immersion tank for removing flaws was about 5 m and the net immersion length was 4.5 m. Plate speed is 4.
The immersion treatment is performed for 60 seconds at 5 m / min and 180 seconds at 1.5 m / min.
【0056】試験 NO.7および8は、図4(d)のタイ
プの装置を用いた場合であり、疵除去用処理はおこなわ
なかった。また、脱スケール用浸漬槽の長さは図4
(a)〜(d)の試験装置共10mであり、正味浸漬長
さは9mなので、通板速度が4.5m/minの場合は
120秒間、1.5m/minの場合は360秒間の浸
漬処理が行われる。表4の実験結果から明らかなよう
に、試験 NO.5〜8の比較例では表面疵の程度が1〜3
であるのに対して、試験 NO.1〜4の本発明例では表面
疵の程度が全て5であり、全く表面疵を無くすることが
できた。Tests No. 7 and No. 8 used the apparatus of the type shown in FIG. 4D, and did not carry out the processing for removing flaws. The length of the immersion tank for descaling is shown in FIG.
(A) to (d) are 10 m and the net immersion length is 9 m. Therefore, when the passing speed is 4.5 m / min, the immersion time is 120 seconds, and when the passing speed is 1.5 m / min, the immersion time is 360 seconds. Processing is performed. As is clear from the experimental results in Table 4, in Comparative Examples of Test Nos. 5 to 8, the degree of surface flaw was 1 to 3
On the other hand, in the examples of the present invention in Test Nos. 1 to 4, the degree of surface flaws was all 5, and the surface flaws could be completely eliminated.
【0057】[0057]
【発明の効果】本発明の方法によれば、人体や環境に有
害で危険性の高い酸類を使用することなく、熱間圧延で
発生した鋼帯の表面疵を容易に除去することができ、製
品の商品価値を高めることができるのみならず、鋼帯製
造の歩留まり(直行率)を高め、製造コストを低減する
ことができるなど産業上大きな利益がある。According to the method of the present invention, it is possible to easily remove the surface flaw of the steel strip generated by hot rolling without using acids which are harmful to the human body and the environment and which are highly dangerous. Not only can the commercial value of the product be increased, but there is also a great industrial benefit, such as the yield of steel strip production (direct rate) can be increased and the production cost can be reduced.
【図1】通電ロールおよび電解液中負極を用いた鋼帯の
陽極電解装置の模式図であるFIG. 1 is a schematic diagram of a steel strip anodic electrolysis apparatus using a current-carrying roll and a negative electrode in an electrolyte solution.
【図2】電解液中の間接通電用負極と正極を用いた鋼帯
の電解装置の模式図である。FIG. 2 is a schematic diagram of a steel strip electrolysis apparatus using a negative electrode and a positive electrode for indirect energization in an electrolytic solution.
【図3】切り板試験片の直接通電による電解実験装置の
模式図である。FIG. 3 is a schematic view of an electrolysis experiment apparatus in which a cut plate test piece is directly energized.
【図4】連続脱スケール−表面疵除去実験装置の構成を
示す模式図である。FIG. 4 is a schematic diagram showing a configuration of a continuous descaling-surface flaw removal experiment apparatus.
1 直流電源 12 脱スケール用塩酸
槽 2 通電ロール 13、14 電解槽 3 負極 15 塩酸槽 4、11 鋼帯 16 スプレー水洗槽 5 電解槽 6 電解液 7 正極 9 試験片DESCRIPTION OF SYMBOLS 1 DC power supply 12 Hydrochloric acid tank for descaling 2 Electricity roll 13, 14 Electrolytic tank 3 Negative electrode 15 Hydrochloric acid tank 4, 11 Steel strip 16 Spray washing tank 5 Electrolytic tank 6 Electrolytic solution 7 Positive electrode 9 Test piece
Claims (2)
溶質の主成分が塩化物である電解液中で陽極電解するこ
とを特徴とする熱延鋼帯の表面疵除去方法。1. A method for removing surface flaws in a hot-rolled steel strip, comprising the step of descaling the hot-rolled steel strip, followed by anodic electrolysis in an electrolytic solution in which the solvent is water and the main component of the solute is chloride.
極として酸化物を被覆した金属チタンからなる電極を用
いて間接通電法により陽極電解することを特徴とする請
求項1記載の熱延鋼帯の表面疵除去方法。2. The hot-rolled steel strip according to claim 1, wherein the anode is made of nickel metal as the negative electrode and the anode is made of metal oxide-coated titanium as the positive electrode by anodic electrolysis by an indirect current applying method. Surface flaw removal method.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP10095972A JPH11293500A (en) | 1998-04-08 | 1998-04-08 | Surface flaw removal method for hot rolled steel strip |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP10095972A JPH11293500A (en) | 1998-04-08 | 1998-04-08 | Surface flaw removal method for hot rolled steel strip |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH11293500A true JPH11293500A (en) | 1999-10-26 |
Family
ID=14152103
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP10095972A Pending JPH11293500A (en) | 1998-04-08 | 1998-04-08 | Surface flaw removal method for hot rolled steel strip |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH11293500A (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2006348336A (en) * | 2005-06-15 | 2006-12-28 | Saitama Prefecture | Electrolytic polishing liquid, and method for producing metal product |
| CN114808094A (en) * | 2022-04-19 | 2022-07-29 | 中国刑事警察学院 | Method and electrolyte for displaying damaged steel frame number |
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|---|---|---|---|---|
| JPS53116231A (en) * | 1977-03-22 | 1978-10-11 | Sumitomo Metal Ind Ltd | Direct electrolytic descaling method for steel wire |
| JPH01208484A (en) * | 1988-02-15 | 1989-08-22 | Nippon Stainless Steel Co Ltd | Polished stainless steel having superior corrosion resistance and production thereof |
| JPH05295599A (en) * | 1992-04-21 | 1993-11-09 | Nippon Steel Corp | High speed pickling method for steel metal |
| JPH07331495A (en) * | 1994-06-13 | 1995-12-19 | Daiso Co Ltd | Insoluble electrode plate fixing part |
| JPH0860400A (en) * | 1994-08-03 | 1996-03-05 | Internatl Business Mach Corp <Ibm> | Method for etching and electric etching apparatus for laminar metal foil |
| JPH08226000A (en) * | 1995-02-14 | 1996-09-03 | Sumitomo Electric Ind Ltd | Electrolytic polishing method for steel wire |
| JPH09241897A (en) * | 1996-03-08 | 1997-09-16 | Dipsol Chem Co Ltd | Pretreatment for surface of magnesium or alloy thereof |
| WO1997038152A1 (en) * | 1996-04-10 | 1997-10-16 | Dynamotive Corporation | A method for removal of films from metal surfaces using electrolysis and cavitation action |
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1998
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Patent Citations (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS53116231A (en) * | 1977-03-22 | 1978-10-11 | Sumitomo Metal Ind Ltd | Direct electrolytic descaling method for steel wire |
| JPH01208484A (en) * | 1988-02-15 | 1989-08-22 | Nippon Stainless Steel Co Ltd | Polished stainless steel having superior corrosion resistance and production thereof |
| JPH05295599A (en) * | 1992-04-21 | 1993-11-09 | Nippon Steel Corp | High speed pickling method for steel metal |
| JPH07331495A (en) * | 1994-06-13 | 1995-12-19 | Daiso Co Ltd | Insoluble electrode plate fixing part |
| JPH0860400A (en) * | 1994-08-03 | 1996-03-05 | Internatl Business Mach Corp <Ibm> | Method for etching and electric etching apparatus for laminar metal foil |
| JPH08226000A (en) * | 1995-02-14 | 1996-09-03 | Sumitomo Electric Ind Ltd | Electrolytic polishing method for steel wire |
| JPH09241897A (en) * | 1996-03-08 | 1997-09-16 | Dipsol Chem Co Ltd | Pretreatment for surface of magnesium or alloy thereof |
| WO1997038152A1 (en) * | 1996-04-10 | 1997-10-16 | Dynamotive Corporation | A method for removal of films from metal surfaces using electrolysis and cavitation action |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2006348336A (en) * | 2005-06-15 | 2006-12-28 | Saitama Prefecture | Electrolytic polishing liquid, and method for producing metal product |
| CN114808094A (en) * | 2022-04-19 | 2022-07-29 | 中国刑事警察学院 | Method and electrolyte for displaying damaged steel frame number |
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