JPH08188900A - Dipping electrolytic deburring method regarding iron - Google Patents

Dipping electrolytic deburring method regarding iron

Info

Publication number
JPH08188900A
JPH08188900A JP98495A JP98495A JPH08188900A JP H08188900 A JPH08188900 A JP H08188900A JP 98495 A JP98495 A JP 98495A JP 98495 A JP98495 A JP 98495A JP H08188900 A JPH08188900 A JP H08188900A
Authority
JP
Japan
Prior art keywords
work
iron
electrolytic
sodium
deburring
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.)
Pending
Application number
JP98495A
Other languages
Japanese (ja)
Inventor
Susumu Kariya
進 苅谷
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Chuo Seisakusho KK
Original Assignee
Chuo Seisakusho KK
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 by Chuo Seisakusho KK filed Critical Chuo Seisakusho KK
Priority to JP98495A priority Critical patent/JPH08188900A/en
Publication of JPH08188900A publication Critical patent/JPH08188900A/en
Pending legal-status Critical Current

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  • Electrical Discharge Machining, Electrochemical Machining, And Combined Machining (AREA)

Abstract

PURPOSE: To deburr a work without especially considering the interval between it and a cathode by anodizing the iron work in an electrolyte contg. halogen compd., ethylene glycol and urea while oscillating the work. CONSTITUTION: An iron work 3 having a burr due to shearing and a cathode 4 are dipped in an electrolyte 2 contg. at least one kind of halogen compd. among KCl, NaCl, KBr, NaBr, KI, NaI, KF and NaF, ethylene glycol or glycerin and urea or EDTA. Anodization is then conducted by impressing a voltage by a DC power source 5 while oscillating the work 3. Consequently, only the sharp angular burr is removed from an ionized boundary layer, and the part is selectively anodized to effectively remove the burr.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明は、陽極となるワークと陰
極との間隔を殊更考慮することなく陽極電解によるバリ
取りを行うことができる鉄を対象とした浸漬電解バリ取
り方法に関するものである。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to an immersion electrolytic deburring method for iron which is capable of deburring by anodic electrolysis without particularly considering the distance between a cathode work and a cathode. .

【0002】[0002]

【従来の技術】従来の電解バリ取り方法は、陽極となる
ワークと陰極とを至近距離に固定し、その間隙に硝酸ナ
トリウム溶液等の電解液を流しながら直流を通電し、陽
極電解によってワーク表面のバリを除去するものであ
る。ところがこの方法ではワークの形状に対応させた陰
極を必要とするうえ、ワークのセッティングが容易では
ないという問題があった。
2. Description of the Related Art In the conventional electrolytic deburring method, a work as an anode and a cathode are fixed at a close distance, a direct current is supplied while an electrolytic solution such as a sodium nitrate solution is flown in the gap, and the work surface is subjected to anodic electrolysis. To remove the burr. However, this method requires a cathode corresponding to the shape of the work, and there is a problem that setting of the work is not easy.

【0003】そこで、陽極となるワークと陰極との間隔
を殊更考慮することなく陽極電解によるバリ取りを行う
ことができる浸漬電解バリ取り方法が提案されている。
この方法は米国特許第4411751 号明細書に示されている
ように、硝酸アンモニウムと、塩化アンモニウムと、ス
ルファミン酸アンモニウムと、エチレングリコールとを
含む電解液中にワークを陰極とともに浸漬し、通電する
方法である。
Therefore, there has been proposed an immersion electrolytic deburring method capable of performing deburring by anodic electrolysis without particularly considering the distance between the work as an anode and the cathode.
As disclosed in U.S. Pat.No. 4411751, this method is a method in which a workpiece is immersed in an electrolyte solution containing ammonium nitrate, ammonium chloride, ammonium sulfamate, and ethylene glycol, and a current is applied. is there.

【0004】この方法は、陽極電解によってワークの表
面に形成されるイオン化界面層を利用したものである。
すなわち、イオン化界面層は陽極電解によるワークの溶
解を制御する役目を果たすものであるが、ワークを揺動
させることによりこのイオン化界面層は溶解し始める。
その溶解の度合いは先鋭な角ほど大きく、そのために電
界が先鋭な角に集中し、ワークのバリを選択的に除去で
きるという原理に基づくものである。
This method utilizes an ionized interface layer formed on the surface of the work by anodic electrolysis.
That is, the ionized interface layer plays a role of controlling the dissolution of the work by anodic electrolysis, but the rocking of the work causes the ionized interface layer to start to dissolve.
The degree of melting is larger at a sharper corner, and therefore the electric field is concentrated on the sharper corner, and the burr of the work can be selectively removed based on the principle.

【0005】この米国特許第4411751 号明細書に示され
た方法によれば、ワークと陰極との間隔を殊更考慮する
ことなく陽極電解によるバリ取りを行うことができる。
しかしこの方法は、ワークがステンレスやアルミニウム
である場合には一応の効果が認められるものの、ワーク
が鉄である場合にはイオン化界面層がごく僅かしか形成
されないため、十分なバリ取り効果を得ることは困難で
あった。
According to the method disclosed in this US Pat. No. 4411751, deburring by anodic electrolysis can be performed without particularly considering the distance between the work and the cathode.
However, this method has some effect when the work is stainless steel or aluminum, but when the work is iron, only a small amount of the ionized interface layer is formed, so a sufficient deburring effect can be obtained. Was difficult.

【0006】[0006]

【発明が解決しようとする課題】本発明は上記した従来
の問題点を解決して、ワークと陰極との間隔を殊更考慮
することなく浸漬電解によってバリ取りすることができ
る鉄を対象とした浸漬電解バリ取り方法を提供するため
になされたものである。
DISCLOSURE OF THE INVENTION The present invention solves the above-mentioned problems of the related art and makes it possible to deburr iron by immersion electrolysis without special consideration of the distance between the work and the cathode. This is done to provide an electrolytic deburring method.

【0007】[0007]

【課題を解決するための手段】上記の課題を解決するた
めになされた本発明は、塩化カリウム、塩化ナトリウ
ム、臭化カリウム、臭化ナトリウム、ヨウ化カリウム、
ヨウ化ナトリウム、フッ化カリウム、フッ化ナトリウム
からなるグループから選択された1種以上のハロゲン化
合物と、エチレングリコールまたはグリセリンと、尿素
またはエチレンジアミン四酢酸とをそれぞれ含有する電
解液中に、陰極と鉄製のワークとを浸漬し、ワークを揺
動しつつ陽極電解を行わせることを特徴とするものであ
る。
The present invention made to solve the above-mentioned problems includes potassium chloride, sodium chloride, potassium bromide, sodium bromide, potassium iodide,
A cathode and an iron-containing material in an electrolytic solution containing one or more halogen compounds selected from the group consisting of sodium iodide, potassium fluoride, and sodium fluoride, ethylene glycol or glycerin, and urea or ethylenediaminetetraacetic acid, respectively. The work is immersed in the work, and the work is rocked to carry out anodic electrolysis.

【0008】[0008]

【作用】本発明によれば、電解液成分として塩化カリウ
ム、塩化ナトリウム、臭化カリウム、臭化ナトリウム、
ヨウ化カリウム、ヨウ化ナトリウム、フッ化カリウム、
フッ化ナトリウムからなるグループから選択された1種
以上のハロゲン化合物を使用したため、鉄製のワーク表
面に不働態化するような不溶解性生成物を生ずることが
ないうえ、電解反応生成物が陰極に付着することもな
い。また、電解液中に尿素またはエチレンジアミン四酢
酸を含有させたので、電解反応生成物がワーク表面に粘
性のある鉄の錯イオン(イオン化界面層)を形成し、さ
らにエチレングリコールまたはグリセリンがこの電解反
応生成物の散逸を防止する。
According to the present invention, potassium chloride, sodium chloride, potassium bromide, sodium bromide, and
Potassium iodide, sodium iodide, potassium fluoride,
Since at least one halogen compound selected from the group consisting of sodium fluoride is used, insoluble products that passivate on the surface of the iron work are not generated, and the electrolytic reaction product acts as the cathode. It does not adhere. Further, since urea or ethylenediaminetetraacetic acid is contained in the electrolytic solution, the electrolytic reaction product forms a viscous iron complex ion (ionized interface layer) on the surface of the work, and further ethylene glycol or glycerin causes this electrolytic reaction. Prevent dissipation of the product.

【0009】このため、本発明によれば鉄製のワーク表
面にイオン化界面層を形成することができ、ワークを揺
動させることによってこのイオン化界面層をバリのよう
な先鋭な角の部分で溶解させ、その部分を選択的に陽極
電解してバリ取りを行うことができる。従って、本発明
によれば従来は不可能であった鉄製のワークのバリ取り
を、ワークと陰極との間隔を殊更考慮することなく行う
ことができる。
Therefore, according to the present invention, the ionized interface layer can be formed on the surface of the iron work, and the ionized interface layer is melted at a sharp corner portion such as a burr by rocking the work. That part can be selectively subjected to anodic electrolysis for deburring. Therefore, according to the present invention, deburring of a work made of iron, which has been impossible in the past, can be performed without further considering the distance between the work and the cathode.

【0010】[0010]

【実施例】以下に本発明を、実施例によって更に詳細に
説明する。図1は本発明の試験装置の概要を示す断面図
であり、1は電解槽、2は電解液、3は剪断によるバリ
を持つ鉄製のワーク(試験片)、4は陰極、5は直流電
源である。実施例のワーク3の材質はSS41(一般構造用
圧延鋼材、P:0.05%以下、S:0.05%以下、残部Fe) であ
り、その寸法は10×10mmである。ワーク3は図示しない
機械的手段によって電解液2中で細かく揺動されてい
る。また陰極4はSUS304からなり、その寸法は50×50mm
であってワーク3に対して平行に約90mmの間隔で設置さ
れている。直流電源5から供給される電解電圧は直流10
Vである。
EXAMPLES The present invention will be described in more detail below with reference to examples. FIG. 1 is a cross-sectional view showing an outline of a test apparatus of the present invention, 1 is an electrolytic cell, 2 is an electrolytic solution, 3 is an iron work (test piece) having a burr by shearing, 4 is a cathode, 5 is a DC power source. Is. The material of the work 3 in the example is SS41 (rolled steel for general structure, P: 0.05% or less, S: 0.05% or less, balance Fe), and its size is 10 × 10 mm. The work 3 is finely swung in the electrolytic solution 2 by a mechanical means (not shown). The cathode 4 is made of SUS304 and its dimensions are 50 x 50 mm.
Therefore, they are installed parallel to the work 3 at intervals of about 90 mm. The electrolysis voltage supplied from the DC power supply 5 is DC 10
V.

【0011】まず予備的な実験として、鉄の陽極電解が
可能な薬品の確認を行った。その結果、塩化カリウム、
塩化ナトリウム、臭化カリウム、臭化ナトリウム、ヨウ
化カリウム、ヨウ化ナトリウム、フッ化カリウム、フッ
化ナトリウムのうちの1種以上を電解成分とした場合に
は、ワーク3の表面が陽極電解された。なお電流密度は
35〜120 A/dm2である。これに対して、酢酸ナトリウ
ム、硝酸ナトリウム、硫酸ナトリウム、炭酸ナトリウ
ム、リン酸三ナトリウム等を電解成分とした場合には、
ワーク3の表面は電解されなかった。次に、電解液2の
組成を種々変化させて試験を行った。その結果は次の通
りである。
First, as a preliminary experiment, chemicals capable of anodic electrolysis of iron were confirmed. As a result, potassium chloride,
When at least one of sodium chloride, potassium bromide, sodium bromide, potassium iodide, sodium iodide, potassium fluoride and sodium fluoride was used as an electrolytic component, the surface of the work 3 was subjected to anodic electrolysis. . The current density is
35 to 120 A / dm 2 . On the other hand, when sodium acetate, sodium nitrate, sodium sulfate, sodium carbonate, trisodium phosphate, etc. are used as electrolytic components,
The surface of the work 3 was not electrolyzed. Next, the test was conducted by changing the composition of the electrolytic solution 2 variously. The results are as follows.

【0012】(実施例1)塩化カリウム100g/L、エチレ
ングリコール400cc/L 、尿素50g/L を含有する電解液を
前記の試験装置の電解槽1に入れ、電流密度40〜50A/dm
2 で90秒間の通電を行い、ワーク3の浸漬電解バリ取り
を行った。その結果、ワーク3の表面は濃い黄色の粘性
のある層で覆われ、滑らかになった。またワーク3の剪
断によるバリは丸みを帯び、優れたバリ取り効果が認め
られた。
(Example 1) An electrolytic solution containing 100 g / L of potassium chloride, 400 cc / L of ethylene glycol, and 50 g / L of urea was placed in the electrolytic cell 1 of the above-mentioned test apparatus, and the current density was 40 to 50 A / dm.
The work 3 was subjected to immersion electrolytic deburring by energizing at 2 for 90 seconds. As a result, the surface of the work 3 was covered with a thick yellow viscous layer and became smooth. Further, burrs due to shearing of the work 3 were rounded, and an excellent deburring effect was recognized.

【0013】(実施例2)塩化カリウム100g/L、エチレ
ングリコール400cc/L 、エチレンジアミン四酢酸50g/L
を含有する電解液を前記の試験装置の電解槽1に入れ、
電流密度40〜50A/dm2 で90秒間の通電を行い、ワーク3
の浸漬電解バリ取りを行った。その結果、ワーク3の表
面は橙色の粘性の少ない層で覆われ、滑らかになった。
またワーク3のバリは丸みを帯び、優れたバリ取り効果
が認められた。
(Example 2) 100 g / L potassium chloride, 400 cc / L ethylene glycol, 50 g / L ethylenediaminetetraacetic acid
An electrolytic solution containing is placed in the electrolytic cell 1 of the above-mentioned test device,
Energize for 90 seconds at a current density of 40 to 50 A / dm 2 and work 3
Immersion electrolytic deburring was performed. As a result, the surface of the work 3 was covered with an orange layer having a low viscosity and became smooth.
Further, the burrs of the work 3 were rounded, and an excellent deburring effect was recognized.

【0014】(実施例3)塩化カリウム100g/L、グリセ
リン400cc/L 、尿素50g/L を含有する電解液を前記の試
験装置の電解槽1に入れ、電流密度27〜38A/dm2 で90秒
間の通電を行い、ワーク3の浸漬電解バリ取りを行っ
た。その結果、ワーク3の表面は黄色の粘性のある層で
覆われ、滑らかになった。またワーク3の剪断によるバ
リは丸みを帯び、優れたバリ取り効果が認められた。
(Example 3) An electrolytic solution containing 100 g / L of potassium chloride, 400 cc / L of glycerin, and 50 g / L of urea was put in the electrolytic cell 1 of the above-mentioned test apparatus, and the current density was 90 at 27 to 38 A / dm 2 . The workpiece 3 was energized for immersion electrolytic deburring of the work 3. As a result, the surface of the work 3 was covered with the yellow viscous layer and became smooth. Further, burrs due to shearing of the work 3 were rounded, and an excellent deburring effect was recognized.

【0015】(実施例4)塩化カリウム100g/L、グリセ
リン400cc/L 、エチレンジアミン四酢酸50g/L を含有す
る電解液を前記の試験装置の電解槽1に入れ、電流密度
27〜38A/dm2 で90秒間の通電を行い、ワーク3の浸漬電
解バリ取りを行った。その結果、ワーク3の表面は橙色
の粘性のある層で覆われ、滑らかになった。またワーク
3のバリは丸みを帯び、優れたバリ取り効果が認められ
た。
(Example 4) An electrolytic solution containing 100 g / L of potassium chloride, 400 cc / L of glycerin, and 50 g / L of ethylenediaminetetraacetic acid was placed in the electrolytic cell 1 of the above-mentioned test apparatus to obtain a current density.
The work 3 was subjected to immersion electrolytic deburring by applying electricity for 90 seconds at 27 to 38 A / dm 2 . As a result, the surface of the work 3 was covered with the orange viscous layer and became smooth. Further, the burrs of the work 3 were rounded, and an excellent deburring effect was recognized.

【0016】(実施例5)臭化カリウム100g/L、エチレ
ングリコール400cc/L 、尿素50g/L を含有する電解液を
前記の試験装置の電解槽1に入れ、電流密度35〜37A/dm
2 で90秒間の通電を行い、ワーク3の浸漬電解バリ取り
を行った。その結果、ワーク3の表面の周辺が橙色の粘
性の少ない層で覆われた。またワーク3の剪断によるバ
リは丸みを帯び、優れたバリ取り効果が認められた。
(Embodiment 5) An electrolytic solution containing 100 g / L of potassium bromide, 400 cc / L of ethylene glycol and 50 g / L of urea was placed in the electrolytic cell 1 of the above-mentioned test apparatus and the current density was 35 to 37 A / dm.
The work 3 was subjected to immersion electrolytic deburring by energizing at 2 for 90 seconds. As a result, the periphery of the surface of the work 3 was covered with an orange layer having a low viscosity. Further, burrs due to shearing of the work 3 were rounded, and an excellent deburring effect was recognized.

【0017】(実施例6)臭化カリウム100g/L、エチレ
ングリコール400cc/L 、エチレンジアミン四酢酸50g/L
を含有する電解液を前記の試験装置の電解槽1に入れ、
電流密度35〜37A/dm2 で90秒間の通電を行い、ワーク3
の浸漬電解バリ取りを行った。その結果、ワーク3の表
面は周辺ほど橙色の粘性のある厚い層で覆われた。また
ワーク3のバリは丸みを帯び、優れたバリ取り効果が認
められた。
Example 6 Potassium bromide 100 g / L, ethylene glycol 400 cc / L, ethylenediaminetetraacetic acid 50 g / L
An electrolytic solution containing is placed in the electrolytic cell 1 of the above-mentioned test device,
Energize for 90 seconds at a current density of 35 to 37 A / dm 2 and work 3
Immersion electrolytic deburring was performed. As a result, the surface of the work 3 was covered with a thick viscous layer having an orange color toward the periphery. Further, the burrs of the work 3 were rounded, and an excellent deburring effect was recognized.

【0018】(実施例7)臭化カリウム100g/L、グリセ
リン400cc/L 、尿素50g/L を含有する電解液を前記の試
験装置の電解槽1に入れ、電流密度23〜26A/dm2 で90秒
間の通電を行い、ワーク3の浸漬電解バリ取りを行っ
た。その結果、ワーク3の表面は周辺が橙色の粘性の少
ない層で覆われた。またワーク3のバリは丸みを帯び、
優れたバリ取り効果が認められた。
(Example 7) An electrolytic solution containing 100 g / L of potassium bromide, 400 cc / L of glycerin and 50 g / L of urea was placed in the electrolytic cell 1 of the above-mentioned test apparatus and the current density was 23 to 26 A / dm 2 . Power was applied for 90 seconds, and the workpiece 3 was subjected to immersion electrolytic deburring. As a result, the periphery of the surface of the work 3 was covered with an orange layer having low viscosity. Also, the burr of the work 3 is rounded,
An excellent deburring effect was recognized.

【0019】(実施例8)臭化カリウム100g/L、グリセ
リン400cc/L 、エチレンジアミン四酢酸50g/L を含有す
る電解液を前記の試験装置の電解槽1に入れ、電流密度
23〜26A/dm2 で90秒間の通電を行い、ワーク3の浸漬電
解バリ取りを行った。その結果、ワーク3の表面は周辺
ほど橙色の粘性のある厚い層で覆われた。またワーク3
のバリは丸みを帯び、優れたバリ取り効果が認められ
た。
(Example 8) An electrolytic solution containing 100 g / L of potassium bromide, 400 cc / L of glycerin, and 50 g / L of ethylenediaminetetraacetic acid was placed in the electrolytic cell 1 of the above-mentioned test apparatus, and the current density was changed.
The workpiece 3 was subjected to immersion electrolytic deburring by energizing at 23 to 26 A / dm 2 for 90 seconds. As a result, the surface of the work 3 was covered with a thick viscous layer having an orange color toward the periphery. Work 3 again
The burr was rounded and an excellent deburring effect was recognized.

【0020】(比較例1)実施例1の塩化カリウムを硝
酸ナトリウムに置き換えた電解液を使用し、他の条件は
実施例1と同一として試験を行ったところ、ワーク3の
表面はほとんど電解されず、バリ取り効果は全く認めら
れなかった。
(Comparative Example 1) A test was conducted using an electrolytic solution in which potassium chloride in Example 1 was replaced with sodium nitrate, and the other conditions were the same as those in Example 1, and the surface of the work 3 was almost electrolyzed. No deburring effect was observed.

【0021】(比較例2)実施例1の尿素をリン酸三ナ
トリウムに置き換えた電解液を使用し、他の条件は実施
例1と同一として試験を行ったところ、ワーク3の表面
は青緑色の層で覆われた。しかしバリは僅かに丸みを帯
びた程度であってバリ取り効果は不十分であった。
(Comparative Example 2) A test was conducted using an electrolytic solution in which urea of Example 1 was replaced with trisodium phosphate and other conditions were the same as those of Example 1, and the surface of the work 3 was bluish green. Covered with layers. However, the burr was slightly rounded and the deburring effect was insufficient.

【0022】(比較例3)実施例1の尿素をトリポリリ
ン酸ナトリウムに置き換えた電解液を使用し、他の条件
は実施例1と同一として試験を行ったところ、ワーク3
の表面は粘性のある黄色の層と白色の層で覆われた。し
かしバリ取り効果は全く認められなかった。
(Comparative Example 3) A test was conducted using an electrolytic solution in which the urea of Example 1 was replaced with sodium tripolyphosphate and the other conditions were the same as those of Example 1.
The surface of was covered with a viscous yellow layer and a white layer. However, no deburring effect was observed.

【0023】[0023]

【発明の効果】以上に説明したように、本発明の浸漬電
解バリ取り方法によれば、鉄製のワークを陰極との間隔
を殊更考慮することなくバリ取りすることができる。こ
のために従来のようにワークの形状に対応させた陰極を
必要とせず、またワークのセッティングが容易となる利
点がある。しかも本発明の電解液は有毒物を含有せず、
バリ取り後のワークの錆の発生を抑える効果もある。よ
って本発明は従来の問題点を解消した鉄を対象とした浸
漬電解バリ取り方法として、業界に大きく寄与するもの
である。
As described above, according to the immersion electrolytic deburring method of the present invention, it is possible to deburr an iron workpiece without further considering the distance from the cathode. For this reason, there is an advantage that a cathode corresponding to the shape of the work is not required unlike the conventional case and the work can be easily set. Moreover, the electrolytic solution of the present invention does not contain toxic substances,
It also has the effect of suppressing the generation of rust on the work after deburring. Therefore, the present invention greatly contributes to the industry as an immersion electrolytic deburring method for iron which solves the conventional problems.

【図面の簡単な説明】[Brief description of drawings]

【図1】実施例及び比較例に用いた試験装置の概要を示
す断面図である。
FIG. 1 is a sectional view showing an outline of a test apparatus used in Examples and Comparative Examples.

【符号の説明】[Explanation of symbols]

1 電解槽 2 電解液 3 鉄製のワーク 4 陰極 5 直流電源 1 Electrolyzer 2 Electrolyte 3 Iron work 4 Cathode 5 DC power supply

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】 塩化カリウム、塩化ナトリウム、臭化カ
リウム、臭化ナトリウム、ヨウ化カリウム、ヨウ化ナト
リウム、フッ化カリウム、フッ化ナトリウムからなるグ
ループから選択された1種以上のハロゲン化合物と、エ
チレングリコールまたはグリセリンと、尿素またはエチ
レンジアミン四酢酸とをそれぞれ含有する電解液中に、
陰極と鉄製のワークとを浸漬し、ワークを揺動しつつ陽
極電解を行わせることを特徴とする鉄を対象とした浸漬
電解バリ取り方法。
1. A halogen compound selected from the group consisting of potassium chloride, sodium chloride, potassium bromide, sodium bromide, sodium bromide, potassium iodide, sodium iodide, potassium fluoride and sodium fluoride, and ethylene. In an electrolytic solution containing glycol or glycerin and urea or ethylenediaminetetraacetic acid, respectively,
An immersion electrolytic deburring method for iron, which comprises immersing a cathode and a work made of iron, and performing anodic electrolysis while rocking the work.
JP98495A 1995-01-09 1995-01-09 Dipping electrolytic deburring method regarding iron Pending JPH08188900A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP98495A JPH08188900A (en) 1995-01-09 1995-01-09 Dipping electrolytic deburring method regarding iron

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP98495A JPH08188900A (en) 1995-01-09 1995-01-09 Dipping electrolytic deburring method regarding iron

Publications (1)

Publication Number Publication Date
JPH08188900A true JPH08188900A (en) 1996-07-23

Family

ID=11488871

Family Applications (1)

Application Number Title Priority Date Filing Date
JP98495A Pending JPH08188900A (en) 1995-01-09 1995-01-09 Dipping electrolytic deburring method regarding iron

Country Status (1)

Country Link
JP (1) JPH08188900A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2001316898A (en) * 2000-05-01 2001-11-16 Chuo Seisakusho Ltd Electro-chemical liquid of aluminum and electro-chemical processing using the same
JP2006348336A (en) * 2005-06-15 2006-12-28 Saitama Prefecture Electrolytic polishing liquid, and method for producing metal product

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2001316898A (en) * 2000-05-01 2001-11-16 Chuo Seisakusho Ltd Electro-chemical liquid of aluminum and electro-chemical processing using the same
JP4497438B2 (en) * 2000-05-01 2010-07-07 株式会社中央製作所 Electrolytic machining liquid for aluminum and electrolytic machining method using the same
JP2006348336A (en) * 2005-06-15 2006-12-28 Saitama Prefecture Electrolytic polishing liquid, and method for producing metal product

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