JP2011106024A - Method for surface treatment of magnesium or magnesium alloy by anodization - Google Patents

Method for surface treatment of magnesium or magnesium alloy by anodization Download PDF

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JP2011106024A
JP2011106024A JP2010112660A JP2010112660A JP2011106024A JP 2011106024 A JP2011106024 A JP 2011106024A JP 2010112660 A JP2010112660 A JP 2010112660A JP 2010112660 A JP2010112660 A JP 2010112660A JP 2011106024 A JP2011106024 A JP 2011106024A
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magnesium
magnesium alloy
surface treatment
anodizing
treatment method
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JP5075940B2 (en
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Hong Gyeun Kim
キム,ホンギュン
Kyu Hwan Seo
ソ,ギュハン
Jae Eun Lee
イ,チェウン
Tae Seung Song
ソン,タスン
Seong Ho Han
ハン,ソンホ
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Korea Institute of Industrial Technology KITECH
KC CHEMICAL CO Ltd
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KC CHEMICAL CO Ltd
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    • CCHEMISTRY; METALLURGY
    • C25ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25DPROCESSES FOR THE ELECTROLYTIC OR ELECTROPHORETIC PRODUCTION OF COATINGS; ELECTROFORMING; APPARATUS THEREFOR
    • C25D11/00Electrolytic coating by surface reaction, i.e. forming conversion layers
    • C25D11/02Anodisation
    • C25D11/30Anodisation of magnesium or alloys based thereon
    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C28/00Coating for obtaining at least two superposed coatings either by methods not provided for in a single one of groups C23C2/00 - C23C26/00 or by combinations of methods provided for in subclasses C23C and C25C or C25D
    • CCHEMISTRY; METALLURGY
    • C25ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25DPROCESSES FOR THE ELECTROLYTIC OR ELECTROPHORETIC PRODUCTION OF COATINGS; ELECTROFORMING; APPARATUS THEREFOR
    • C25D11/00Electrolytic coating by surface reaction, i.e. forming conversion layers
    • C25D11/02Anodisation
    • C25D11/026Anodisation with spark discharge

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  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Materials Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
  • Electrochemistry (AREA)
  • Mechanical Engineering (AREA)
  • Cleaning And De-Greasing Of Metallic Materials By Chemical Methods (AREA)
  • Chemical Treatment Of Metals (AREA)
  • Other Surface Treatments For Metallic Materials (AREA)

Abstract

<P>PROBLEM TO BE SOLVED: To provide a method for the surface treatment of magnesium or a magnesium alloy by anodization to form an anodized oxide coating on the magnesium or magnesium alloy. <P>SOLUTION: The method of surface treatment by anodizing comprises: a pretreatment step of removing impurities and an oxide layer present on the surface of magnesium or a magnesium alloy using a strongly alkaline aqueous solution; and a micro-arc plasma anodization step of immersing the pre-treated magnesium or magnesium alloy in an alkaline electrolyte and applying a direct current having a current density of 3 A/dm<SP>2</SP>or less to the electrolyte to form a magnesium oxide coating. <P>COPYRIGHT: (C)2011,JPO&INPIT

Description

本発明は、マグネシウム又はマグネシウム合金の耐食性向上のための表面処理方法に関するものであり、より詳しくは、クロム及びマンガン成分等のような環境汚染物質が含まれない環境に優しい電解液を使用して劇毒廃水の発生を源泉的に止揚し、塗装の下地用として耐食性及び塗装密着性を向上させたマグネシウム又はマグネシウム合金の環境に優しい表面処理方法に関するものである。   The present invention relates to a surface treatment method for improving the corrosion resistance of magnesium or a magnesium alloy. More specifically, the present invention uses an environmentally friendly electrolyte containing no environmental pollutants such as chromium and manganese components. The present invention relates to an environmentally friendly surface treatment method for magnesium or a magnesium alloy, which is a source of fulminant wastewater and has improved corrosion resistance and paint adhesion as a base for painting.

一般的に、マグネシウムは、地球上で6番目に豊富な金属として知られており、比重がアルミニウムの約2/3程度で、常用される金属中最も軽く、優れた比強度(強度/比重)、耐力、優れた電磁波遮蔽性、及び優れた振動吸着力等のような長所を有している。このような長所のため、マグネシウム合金は、ハウジング、オイルファン、シートフレーム等のような自動車用部品、携帯用ノート型パソコン、携帯電話ケース類、レジャー及びスポーツ用品、先端宇宙航空素材等に幅広く適用されたり、又はそのような適用が試みられている。   In general, magnesium is known as the sixth most abundant metal on earth, and its specific gravity is about 2/3 that of aluminum. It is the lightest of all commonly used metals and has excellent specific strength (strength / specific gravity). It has advantages such as proof stress, excellent electromagnetic shielding properties, and excellent vibration adsorption power. Because of these advantages, magnesium alloys are widely applied to automotive parts such as housings, oil fans, seat frames, portable notebook computers, mobile phone cases, leisure and sports equipment, advanced aerospace materials, etc. Or such applications have been attempted.

マグネシウム合金は、多くの優れた長所を有している反面、活性化の傾向が大きい金属のため、アルカリと酸に脆弱だという短所を有する。よって、マグネシウム又はマグネシウム合金が腐食環境に露出されると深刻なガルバニック腐食が進行するため、マグネシウム又はマグネシウム合金表面は耐食性に優れた有機又は無機コーティングが必ず要求される。   Magnesium alloys have many excellent advantages, but are disadvantageous in that they are vulnerable to alkalis and acids because they are metals that have a high tendency to be activated. Therefore, when magnesium or a magnesium alloy is exposed to a corrosive environment, serious galvanic corrosion proceeds. Therefore, an organic or inorganic coating excellent in corrosion resistance is always required on the surface of magnesium or magnesium alloy.

マグネシウム合金の表面処理方法には、乾式コーティング方法と湿式コーティング方法がある。乾式コーティング方法は、高い蒸気圧のため真空中での蒸着メッキが困難で、作業空間の限界及び高い製造原価等によって多くの制約を受けている。   As the surface treatment method of the magnesium alloy, there are a dry coating method and a wet coating method. In the dry coating method, vapor deposition plating in a vacuum is difficult due to a high vapor pressure, and there are many restrictions due to limitations of working space and high manufacturing costs.

湿式コーティング方法の場合、マグネシウム合金は活性化の傾向が大きいため、電解メッキ又は無電解メッキによる表面コーティング過程中にマグネシウムイオンと電解液内のイオンがマグネシウム合金表面に相互置換反応を起こし、これは電解液の老化度を深刻化させ、メッキされた表面の耐食性もガルバニック腐食によって大きく落ちるため、付加価値が低いという短所がある。   In the case of the wet coating method, since the magnesium alloy has a large activation tendency, magnesium ions and ions in the electrolytic solution cause a mutual substitution reaction on the surface of the magnesium alloy during the surface coating process by electrolytic plating or electroless plating. Since the aging degree of the electrolytic solution is made serious and the corrosion resistance of the plated surface is greatly reduced by galvanic corrosion, the added value is low.

上のような問題点を解決するためのマグネシウム合金の表面処理方法の代案として化成皮膜処理方法があり、代表的な化成皮膜処理方法としてはクロム酸系と非クロム酸系化成処理方法がある。これらの方法は、皮膜の耐食性と耐磨耗性がさほど良くなく、塗装の前処理用に制限的に使用されている実情であり、また、皮膜形成のために公害問題として規制が予想されるクロム(Cr)又はマンガン(Mn)を使用しているため、今後の生産過程に規制が伴う可能性が大きいという決定的な短所がある。   As an alternative to the surface treatment method of magnesium alloy for solving the above problems, there is a chemical conversion film treatment method, and representative chemical conversion film treatment methods include chromic acid-based and non-chromic acid-based chemical conversion treatment methods. In these methods, the corrosion resistance and abrasion resistance of the film are not so good, and they are used in a limited way for pretreatment of coating, and regulation is expected as a pollution problem for film formation. Since chromium (Cr) or manganese (Mn) is used, there is a decisive disadvantage that there is a high possibility that the production process will be regulated in the future.

また、陽極酸化法によるマグネシウム合金のコーティング技術があるが、これはガルバニックアノダイジング(Galvanic anodizing)、HAEアノダイジング、Dow 17アノダイジング等の方法で多くの研究がなされた。   Also, there is a magnesium alloy coating technique by an anodic oxidation method, and many studies have been made by methods such as galvanic anodizing, HAE anodizing, and Dow 17 anodizing.

しかし、マグネシウム又はマグネシウム合金の陽極酸化法は、Al及びAl合金の非晶質陽極酸化処理と比較すると、酸化皮膜が形成される電解液のpH、電解液の種類と反応原理が異なり、マグネシウムの酸化時に発生する酸化皮膜の膨張率がむしろ縮小する形態で皮膜が形成されるため、陽極酸化皮膜は内部加工が多く生じ皮膜の緻密度が低くなり、これと関連して耐食性も低くなるという問題点があった。そして、陽極酸化法もやはり、皮膜処理方法と同様に処理液の組成に公害問題を発生させ得るクロムとマンガンを使用しているという問題点があった。図1は、従来の陽極酸化方法を表す図面であり、これを参照すると、マグネシウム又はマグネシウム合金表面の脱脂、水洗い、酸化層除去、水洗い、陽極酸化、水洗い、乾燥の段階を順に経てマグネシウム又はマグネシウム合金表面に皮膜層を形成する。   However, the anodizing method of magnesium or magnesium alloy differs from the amorphous anodic oxidation treatment of Al and Al alloy in the pH of the electrolyte solution on which the oxide film is formed, the type of electrolyte solution and the reaction principle, Since the film is formed in such a form that the expansion rate of the oxide film generated during oxidation is rather reduced, the anodized film has a large amount of internal processing, and the density of the film is lowered, and in this connection, the corrosion resistance is also lowered. There was a point. The anodic oxidation method also has a problem in that it uses chromium and manganese, which can cause pollution problems in the composition of the treatment liquid, as in the film treatment method. FIG. 1 is a diagram showing a conventional anodizing method. Referring to FIG. 1, magnesium or magnesium is sequentially subjected to steps of degreasing, washing with water, removing an oxide layer, washing with water, anodizing, washing with water, and drying. A coating layer is formed on the alloy surface.

このような問題点を解決するために、プラズマ陽極酸化又は微細アーク陽極酸化等の名前に変形された技術が開発されている。このような技術は、共通してSi4+イオンが含有された電解液を使用して、高電圧(150V〜500V)上で表面のアーク形成強度を高め皮膜の内部加工にSi4+イオンをマグネシウムシリケートの形態で満たして緻密な組織を作る方法だった。しかし、上のような高電圧陽極酸化方法は、マグネシウム部品の量産化のために整流器容量が非常に大きくなってしまい、酸化皮膜は堅固ではあるが軟性のないセラミックのため多くのクラックを発生させ、耐食性向上のための後処理塗装の密着性が悪いという短所がある。代案として、直流/交流重畳方法やパルス電源方法で高電圧を低くさせようとする様々な努力があったが、常用化の結果は整流器が高価であるのに対し、それに準ずる効果は大きくなかった。 In order to solve such a problem, a technique modified to a name such as plasma anodization or fine arc anodization has been developed. Such a technique uses a common electrolyte containing Si 4+ ions to increase the surface arc formation strength on a high voltage (150V to 500V), and to convert Si 4+ ions into magnesium silicate for internal processing of the coating. It was a method of filling in the form of and making a dense organization. However, the high voltage anodic oxidation method as described above has a very large rectifier capacity due to the mass production of magnesium parts, and the oxide film is a firm but non-soft ceramic that generates many cracks. In addition, there is a disadvantage that the adhesion of the post-treatment coating for improving the corrosion resistance is poor. As an alternative, there were various efforts to lower the high voltage by the DC / AC superposition method or the pulse power supply method, but the result of normalization was that the rectifier was expensive, but the effect equivalent to it was not great .

また、陽極酸化前の前処理工程でサンドブラストを使用する場合があるが、この場合、マグネシウム表面の油等の異物質除去が十分にされないため、陽極酸化皮膜の不良を誘導し得、有機溶剤であるTCE(トリクロロエチレン)又はアセトン等を使用する場合があるが、この場合は深刻な公害を誘発し得るため注意を要する。   In addition, sand blasting may be used in the pretreatment step before anodization. In this case, since foreign substances such as oil on the surface of magnesium are not sufficiently removed, defects in the anodized film can be induced. Some TCE (trichloroethylene) or acetone may be used, but care must be taken in this case because it may induce serious pollution.

よって、本発明は、前記のような表面処理の問題点を解決するために案出されたものであり、前処理工程の改善、そして環境に害のない電解液での低電圧直流電流を加える微細アークプラズマ陽極酸化処理方法を利用して、マグネシウム又はマグネシウム合金母材の表面に特性の良い陽極酸化皮膜を形成する技術を提供することを目的とする。   Therefore, the present invention has been devised to solve the problems of the surface treatment as described above, and improves the pretreatment process and applies a low voltage direct current in an electrolyte solution that is not harmful to the environment. An object of the present invention is to provide a technique for forming an anodic oxide film having good characteristics on the surface of a magnesium or magnesium alloy base material by using a fine arc plasma anodizing method.

本発明の他の目的は、前処理工程の改善を通じて脱脂不良の問題及び有機廃水の発生を大きく減少させ、クロム及びマンガン成分を含有しないため環境に優しく、Si4+イオンが含まれない電解液で低電圧直流電流を加える微細アークプラズマ陽極酸化処理方法を利用して特性の良い陽極酸化皮膜を形成する技術を提供することである。 Another object of the present invention is to reduce the problem of degreasing failure and the generation of organic wastewater through the improvement of the pretreatment process, and is environmentally friendly because it does not contain chromium and manganese components, and it is an electrolyte solution that does not contain Si 4+ ions. It is an object of the present invention to provide a technique for forming an anodic oxide film having good characteristics by utilizing a fine arc plasma anodizing method for applying a low-voltage direct current.

本発明の一実施例によるマグネシウム又はマグネシウム合金に酸化膜を形成させるためのマグネシウム又はマグネシウム合金の陽極酸化表面処理方法は、強アルカリの水溶液を利用してマグネシウム又はマグネシウム合金表面の異物質と酸化層を除去する前処理工程と、該前処理工程を経たマグネシウム又はマグネシウム合金をアルカリ電解液中に浸した後、電流密度が3A/dm以下の直流電流を加えてマグネシウム酸化物の皮膜コーティング層を形成する微細アークプラズマ陽極酸化工程を含む。このとき、前記アルカリ電解液中にはSi4+イオンが含まれない。 According to an embodiment of the present invention, an anodized surface treatment method of magnesium or a magnesium alloy for forming an oxide film on the magnesium or the magnesium alloy is performed by using a strong alkaline aqueous solution and a foreign substance and an oxide layer on the surface of the magnesium or the magnesium alloy. And a magnesium oxide film coating layer by applying a direct current with a current density of 3 A / dm 2 or less after immersing the magnesium or magnesium alloy that has undergone the pretreatment step in an alkaline electrolyte. Including a fine arc plasma anodizing step to form. At this time, Si 4+ ions are not included in the alkaline electrolyte.

本発明の一実施例による陽極酸化表面処理方法は、前記微細アークプラズマ陽極酸化工程後に前記皮膜コーティング層が形成されたマグネシウム又はマグネシウム合金を蒸留水で洗浄した後、熱風で乾燥する後処理工程をさらに含む。   An anodic oxidation surface treatment method according to an embodiment of the present invention includes a post-treatment step of washing magnesium or a magnesium alloy on which the coating layer is formed after the fine arc plasma anodization step with distilled water and then drying with hot air. In addition.

好ましくは、該前処理工程の強アルカリ水溶液は、KOH 30g/L〜60g/L、NaOH 150g/L〜200g/L、アミンオキシド20g/L〜30g/L、α−アルコキシイソブチル酸アルキルエステル5g/L〜10g/L、浸潤剤(Wetting agent)を含む。   Preferably, the strong alkaline aqueous solution in the pretreatment step is KOH 30 g / L to 60 g / L, NaOH 150 g / L to 200 g / L, amine oxide 20 g / L to 30 g / L, α-alkoxyisobutyric acid alkyl ester 5 g / L. L to 10 g / L, including a wetting agent.

好ましくは、前記微細アークプラズマ陽極酸化工程の前記アルカリ電解液は、水酸化カリウム(KOH) 20〜150g/L、炭酸ナトリウム(Na2CO3)20〜150g/L、クエン酸三ナトリウム(Trisodium citrate)5〜40g/L、フッ化カリウム(KF)3〜40g/L、酸性フッ化アンモニウム(NH4HF2)3〜40g/Lを含む。各成分別の含量が上の組成比より低かったり高い範囲では、母材表面に陽極酸化皮膜が形成される速度が過度に遅くなったり、膜表面が焦げる現象が起こり不均一な皮膜が形成される恐れがある[表2参照]。 Preferably, the alkaline electrolyte in the fine arc plasma anodizing step includes potassium hydroxide (KOH) 20 to 150 g / L, sodium carbonate (Na 2 CO 3 ) 20 to 150 g / L, trisodium citrate (Trisodium citrate). ) 5-40 g / L, potassium fluoride (KF) 3-40 g / L, acidic ammonium fluoride (NH 4 HF 2 ) 3-40 g / L. In the range where the content of each component is lower or higher than the above composition ratio, the rate at which the anodic oxide film is formed on the surface of the base material becomes excessively slow, or the film surface burns and a non-uniform film is formed. [See Table 2].

本発明は、陽極酸化処理前の前処理工程として、TCE(トリクロロエチレン)、アセトンのような有機溶剤又は脱脂効果が低いサンドブラストを利用する既存の前処理工程の代わりに、環境に優しい強アルカリ水溶液を利用した脱脂工程を含む前処理工程を行うことにより、該前処理工程がより単純になるだけでなく、前処理工程を通じて陽極酸化皮膜が形成される加工表面がそのまま維持され、製品不良率を最小化するという効果がある。また、従来の前処理工程で排出される有機廃水の発生や、サンドブラストで生成されるマグネシウム粉塵の発生を源泉的に抑制するという効果がある。   In the present invention, instead of an existing pretreatment step using an organic solvent such as TCE (trichloroethylene) or acetone or sandblasting with low degreasing effect as a pretreatment step before anodizing treatment, an environmentally friendly strong alkaline aqueous solution is used. By performing the pretreatment process including the used degreasing process, not only the pretreatment process becomes simpler, but also the processed surface on which the anodized film is formed through the pretreatment process is maintained as it is, and the product defect rate is minimized. There is an effect of becoming. In addition, there is an effect that the generation of organic waste water discharged in the conventional pretreatment process and the generation of magnesium dust generated by sandblasting are suppressed in a source manner.

本発明は、微細アークプラズマ陽極酸化工程において、クロム及び/又はマンガン成分のような環境汚染物質ではない、環境に優しく入手が容易な電解質溶液を使用することにより、廃水の発生を源泉的に抑制するという効果がある。   The present invention suppresses the generation of wastewater by using an electrolyte solution that is not an environmental pollutant such as chromium and / or manganese components and is easily available in the micro arc plasma anodizing process. There is an effect of doing.

また、本発明は、炭酸ナトリウム(Na2CO3)が添加された電解質溶液を利用した微細アークプラズマ陽極酸化工程により、従来に比べ緻密なマグネシウム酸化物の陽極酸化皮膜層を形成でき、陽極酸化皮膜層表面に微細且つ均一な突起状のマグネシウム化合物を形成することにより、後工程である塗装の密着性を極大化させ、耐食性、耐摩耗性及び塗装性を向上させる効果がある。 Further, according to the present invention, a fine arc plasma anodic oxidation process using an electrolyte solution to which sodium carbonate (Na 2 CO 3 ) is added can form a dense magnesium oxide anodic oxide film layer as compared with the prior art. By forming a fine and uniform protruding magnesium compound on the surface of the coating layer, there is an effect of maximizing the adhesion of the coating, which is a subsequent process, and improving the corrosion resistance, wear resistance, and paintability.

従来のマグネシウム又はマグネシウム合金の表面に陽極酸化皮膜を形成する表面処理方法を図示した順序図Flow chart illustrating a conventional surface treatment method for forming an anodized film on the surface of magnesium or magnesium alloy 本発明の一実施例にかかるマグネシウム又はマグネシウム合金の表面に陽極酸化皮膜を形成する表面処理方法を図示した順序図1 is a flow chart illustrating a surface treatment method for forming an anodized film on the surface of magnesium or a magnesium alloy according to an embodiment of the present invention. 図2に図示した表面処理方法で表面処理されたマグネシウム合金板材表面の組織拡大写真Structure enlarged photograph of the surface of the magnesium alloy sheet surface-treated by the surface treatment method shown in FIG.

以下、添付する図面を参照して本発明の実施例を詳しく説明する。本実施例は、当業者に本考案の思想が十分に伝わるようにするために例で以って提供する。よって、本考案は、以下で説明する実施例に限定されず、他の形態で具体化することもできる。   Hereinafter, embodiments of the present invention will be described in detail with reference to the accompanying drawings. This embodiment is provided by way of example so that those skilled in the art can fully understand the idea of the present invention. Therefore, the present invention is not limited to the embodiments described below, and can be embodied in other forms.

図2は、本発明にかかる陽極酸化表面処理方法を概略的に表した順序図である。これを参照すると、本発明にかかる表面処理方法は、アルカリ脱脂工程(S10)、微細アークプラズマ陽極酸化工程(S20)及び乾燥工程(S30)を含む。アルカリ脱脂工程(S10)と微細アークプラズマ陽極酸化工程(S20)の間、そして微細アークプラズマ陽極酸化工程(S20)と乾燥工程(S30)の間には、水洗い工程(S12、S22)が行われる。   FIG. 2 is a flow chart schematically showing the anodizing surface treatment method according to the present invention. Referring to this, the surface treatment method according to the present invention includes an alkali degreasing step (S10), a fine arc plasma anodizing step (S20), and a drying step (S30). A water washing step (S12, S22) is performed between the alkaline degreasing step (S10) and the fine arc plasma anodizing step (S20) and between the fine arc plasma anodizing step (S20) and the drying step (S30). .

アルカリ脱脂工程(S10)では、マグネシウム又はマグネシウム合金母材を強アルカリ水溶液に浸して表面に強く付着している有機物を表面で化学反応によって溶解して溶かす脱脂処理をすると同時に表面に残存する異物質を除去する。脱脂処理された母材は、水洗い工程(S12)を経た後、脱脂処理と水洗いを経た母材表面に炭酸マグネシウムを含むマグネシウム酸化層皮膜が形成される微細アークプラズマ陽極酸化工程(S20)が行われる。次に、陽極酸化皮膜層を水洗いする工程(S22)と陽極酸化皮膜層を乾燥する工程(S30)が順に行われる。   In the alkaline degreasing step (S10), a foreign substance remaining on the surface at the same time as the degreasing treatment in which magnesium or a magnesium alloy base material is immersed in a strong alkaline aqueous solution to dissolve and dissolve the organic matter strongly adhered to the surface by a chemical reaction. Remove. The degreased base material is subjected to a water washing step (S12), followed by a fine arc plasma anodizing step (S20) in which a magnesium oxide layer film containing magnesium carbonate is formed on the surface of the base material subjected to the degreasing treatment and water washing. Is called. Next, the step of washing the anodized film layer (S22) and the step of drying the anodized film layer (S30) are sequentially performed.

先ず、アルカリ脱脂工程(S10)では、アミンオキシドとアルカリ成分によって表面に付いている加工油と離型剤等を油化させ、油化された油をα−アルコキシイソブチル酸アルキルエステルで分散させて水溶液に溶解させて表面をきれいにする。より具体的には、前記アルカリ脱脂工程は、KOH 30g/L〜60g/L、NaOH 150g/L〜200g/L、アミンオキシド20g/L〜30g/L、α−アルコキシイソブチル酸アルキルエステル5g/L〜10g/L、浸潤剤で組成された約35〜50℃の強アルカリ水溶液内にマグネシウム合金を浸漬する方式で行われる。各成分別含量が上の各組成比より低かったり高い範囲では表面の油成分が除去される速度が非常に遅かったり、又は母材表面の変色が起こり得る。よって、上記組成比のアルカリ水溶液内で脱脂工程が行われることが好ましい。   First, in the alkaline degreasing step (S10), the processing oil attached to the surface by the amine oxide and the alkali component, the release agent and the like are oiled, and the oiled oil is dispersed with an α-alkoxyisobutyric acid alkyl ester. Dissolve in aqueous solution to clean the surface. More specifically, the alkali degreasing step includes KOH 30 g / L to 60 g / L, NaOH 150 g / L to 200 g / L, amine oxide 20 g / L to 30 g / L, α-alkoxyisobutyric acid alkyl ester 5 g / L. It is performed by immersing the magnesium alloy in a strong alkaline aqueous solution of about 35 to 50 ° C. composed of 10 to 10 g / L and a wetting agent. When the content of each component is lower or higher than the above composition ratios, the speed at which the oil component on the surface is removed may be very slow, or discoloration of the base material surface may occur. Therefore, it is preferable that the degreasing step is performed in an alkaline aqueous solution having the above composition ratio.

次に、微細アークプラズマ陽極酸化工程(S20)では水酸化カリウムと炭酸ナトリウムが主成分の環境に優しい電解液中にマグネシウム製品を浸した後、電流密度が3A/dm以下の範囲内で直流電流を加える。
前記の環境に優しい電解液は、pH9〜14のアルカリ電解液が使われ、その組成及び濃度は下記の[表1]の通りである。ここで、陽極酸化と同時にカラーリングをしたり、マグネシウム製品の成分変化が深刻な場合は、状況に応じて若干の添加剤を別途に添加できる。
Next, in the fine arc plasma anodizing step (S20), the magnesium product is immersed in an environmentally friendly electrolyte mainly composed of potassium hydroxide and sodium carbonate, and then the direct current is within a range where the current density is 3 A / dm 2 or less. Apply current.
As the environmentally friendly electrolyte, an alkaline electrolyte having a pH of 9 to 14 is used, and its composition and concentration are as shown in [Table 1] below. Here, when coloring is performed simultaneously with anodic oxidation, or when the component change of the magnesium product is serious, some additives can be added separately depending on the situation.

電解液は、マンガン及びクロムを使用しない環境に優しい電解液を使用することに特徴があり、特に前記電解液の組成中で炭酸ナトリウム(Na2CO3)を多量添加することにより、微細アークプラズマ陽極酸化反応で生成される酸化マグネシウムの緻密ではない皮膜中に炭酸マグネシウムの不溶性皮膜が緻密に満たされ、皮膜の表面に突起状の炭酸マグネシウムとクエン酸三ナトリウムの反応生成物が形成されるが、これは陽極酸化後に塗装の密着性を向上させる重要な役割をすることになる。 The electrolytic solution is characterized in that it uses an environmentally friendly electrolytic solution that does not use manganese and chromium. In particular, by adding a large amount of sodium carbonate (Na 2 CO 3 ) in the composition of the electrolytic solution, a fine arc plasma is used. The insoluble film of magnesium carbonate is densely filled in the non-dense film of magnesium oxide produced by the anodic oxidation reaction, and a reaction product of protruding magnesium carbonate and trisodium citrate is formed on the surface of the film. This will play an important role in improving the adhesion of the coating after anodization.

図3は、炭酸ナトリウムを添加した電解液を利用した微細アーク陽極酸化処理後、マグネシウム酸化層の緻密な組織構成と表面の突起を表す写真である。   FIG. 3 is a photograph showing the fine structure of the magnesium oxide layer and the protrusions on the surface after the fine arc anodizing treatment using the electrolytic solution added with sodium carbonate.

一方、前記電解液の電流効率は100%であり、これにより皮膜形成率が非常に高いため、3A/dm以下の低い電流密度でも微細アークプラズマ陽極酸化反応が可能である。また、45V〜70Vの低い微細アーク形成電圧で酸化皮膜が形成されるため、整流器の容量も大量生産時に問題にならないという長所がある。 On the other hand, the current efficiency of the electrolytic solution is 100%, and thus the film formation rate is very high, so that a fine arc plasma anodic oxidation reaction is possible even at a low current density of 3 A / dm 2 or less. Further, since the oxide film is formed at a low arc forming voltage of 45V to 70V, there is an advantage that the capacity of the rectifier is not a problem at the time of mass production.

ここで、[表2]に示したような電解液組成で本発明の微細アークプラズマ陽極酸化処理をマグネシウム合金板材(AZ31)に20分実施した後、蒸留水で水洗いを徹底的に行い、熱風乾燥を120℃で5分実施し、冷却して塩水噴霧試験を実施した結果を表した。   Here, after carrying out the fine arc plasma anodizing treatment of the present invention on the magnesium alloy plate (AZ31) for 20 minutes with the electrolytic solution composition as shown in [Table 2], it was thoroughly washed with distilled water, The results of drying for 5 minutes at 120 ° C., cooling, and a salt spray test were shown.

塗装をしない状態でも、本発明の微細アークプラズマ陽極酸化条件で生成された皮膜は48時間何ら異常がない優れた耐食性を表した。   Even without coating, the film produced under the fine arc plasma anodizing conditions of the present invention exhibited excellent corrosion resistance without any abnormality for 48 hours.

本発明によって10分間陽極酸化処理されたマグネシウム合金板材(AZ31)に塗装を実施した結果、塩水噴霧240時間にも何ら腐食の痕跡が現れないことから、10分程度の陽極酸化によって得られた皮膜は十分な密着性を有する塗装下地用として使用できるという大きな長所がある。   As a result of coating on the magnesium alloy plate (AZ31) anodized for 10 minutes according to the present invention, no traces of corrosion appear even after 240 hours of salt water spraying, so that the film obtained by anodization for about 10 minutes Has a great advantage that it can be used as a coating base having sufficient adhesion.

本発明は、マグネシウム合金の塗装下地用として適した陽極酸化処理方法である。これに対してより具体的に説明すると、電解液の混濁性と板状熱交換器の詰り現象を誘発するシリケート成分が電解液内に含まれず、水溶液中で直流電源でマグネシウム合金素材を陽極にして一定の電流密度で電解反応を起こすと、初期には一定の速度で電圧が上昇するが、45Vから70V間で水溶液に浸かっているマグネシウム合金表面に誘電破壊による微細アークプラズマが発生しながら、表面に微細アーク発生時に生じた孔が多くの灰白色のマグネシウム酸化物皮膜を形成する。この孔は後の工程で塗装をする際に密着性を大きく向上させて耐食性と耐磨耗性に優れた塗膜を得ることができるようにする。
The present invention is an anodizing method suitable for use as a base coating for a magnesium alloy. More specifically, the silicate component that induces turbidity of the electrolyte and clogging of the plate heat exchanger is not included in the electrolyte, and the magnesium alloy material is used as an anode with a DC power source in an aqueous solution. When an electrolytic reaction occurs at a constant current density, the voltage rises at a constant rate in the initial stage, while a fine arc plasma due to dielectric breakdown is generated on the surface of the magnesium alloy immersed in an aqueous solution between 45V and 70V. The holes generated when a fine arc is generated on the surface form many grayish white magnesium oxide films. This hole greatly improves the adhesion when coating in a later step so that a coating film excellent in corrosion resistance and wear resistance can be obtained.

Claims (5)

マグネシウム又はマグネシウム合金に酸化膜を形成させるための陽極酸化表面処理方法において、
強アルカリの水溶液を利用してマグネシウム又はマグネシウム合金表面の異物質と酸化層を除去する前処理工程と;
該前処理工程を経たマグネシウム又はマグネシウム合金をアルカリ電解液中に浸した後、電流密度が3A/dm以下の直流電流を加えてマグネシウム酸化物の皮膜コーティング層を形成する微細アークプラズマ陽極酸化工程と
を含むことを特徴とする、マグネシウム又はマグネシウム合金の陽極酸化表面処理方法。
In the anodized surface treatment method for forming an oxide film on magnesium or a magnesium alloy,
A pretreatment step of removing foreign substances and oxide layers on the surface of magnesium or a magnesium alloy using a strong alkaline aqueous solution;
A fine arc plasma anodizing step of forming a magnesium oxide film coating layer by immersing magnesium or a magnesium alloy that has undergone the pretreatment step in an alkaline electrolyte and then applying a direct current with a current density of 3 A / dm 2 or less. And a method for anodizing surface treatment of magnesium or a magnesium alloy.
前記微細アークプラズマ陽極酸化工程後に、前記皮膜コーティング層が形成されたマグネシウム又はマグネシウム合金を蒸留水で洗浄した後、熱風で乾燥する後処理工程をさらに含むことを特徴とする、請求項1に記載のマグネシウム又はマグネシウム合金の陽極酸化表面処理方法。   2. The method according to claim 1, further comprising a post-treatment step of washing the magnesium or the magnesium alloy on which the film coating layer is formed with distilled water after the fine arc plasma anodizing step and then drying with hot air. Anodizing surface treatment method of magnesium or magnesium alloy. 前記前処理工程の強アルカリ水溶液は、KOH 30g/L〜60g/L、NaOH 150g/L〜200g/L、アミンオキシド20g/L〜30g/L、α−アルコキシイソブチル酸アルキルエステル5g/L〜10g/L、浸潤剤(Wetting agent)を含むことを特徴とする、請求項1に記載のマグネシウム又はマグネシウム合金の陽極酸化表面処理方法。   The strong alkaline aqueous solution in the pretreatment step is KOH 30 g / L to 60 g / L, NaOH 150 g / L to 200 g / L, amine oxide 20 g / L to 30 g / L, α-alkoxyisobutyric acid alkyl ester 5 g / L to 10 g. 2. The anodizing surface treatment method for magnesium or a magnesium alloy according to claim 1, comprising / L and a wetting agent. 前記微細アークプラズマ陽極酸化工程の前記アルカリ電解液は炭酸ナトリウム(Na2CO3)を含むことを特徴とする、請求項1に記載のマグネシウム又はマグネシウム合金の陽極酸化表面処理方法。 Wherein said alkaline electrolyte fine plasma anodization process is characterized in that it comprises sodium carbonate (Na 2 CO 3), anodized surface treatment method of the magnesium or magnesium alloy of claim 1. 前記微細アークプラズマ陽極酸化工程の前記アルカリ電解液は、水酸化カリウム(KOH)20〜150g/L、炭酸ナトリウム(Na2CO3)20〜150g/L、クエン酸三ナトリウム(Tri Sodium Citrate)5〜40g/L、フッ化カリウム(KF)3〜40g/L、酸性フッ化アンモニウム(NH4HF2)3〜40g/Lを含むことを特徴とする、請求項1に記載のマグネシウム又はマグネシウム合金の陽極酸化表面処理方法。
The alkaline electrolyte in the fine arc plasma anodizing step includes potassium hydroxide (KOH) 20 to 150 g / L, sodium carbonate (Na 2 CO 3 ) 20 to 150 g / L, trisodium citrate 5 to 40 g / L, characterized in that it comprises a potassium fluoride (KF) 3~40g / L, ammonium bifluoride (NH 4 HF 2) 3~40g / L, magnesium or magnesium alloy according to claim 1 Anodizing surface treatment method.
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