JPH0442434B2 - - Google Patents
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- Publication number
- JPH0442434B2 JPH0442434B2 JP3992483A JP3992483A JPH0442434B2 JP H0442434 B2 JPH0442434 B2 JP H0442434B2 JP 3992483 A JP3992483 A JP 3992483A JP 3992483 A JP3992483 A JP 3992483A JP H0442434 B2 JPH0442434 B2 JP H0442434B2
- Authority
- JP
- Japan
- Prior art keywords
- corrosion
- hydrotalcite
- paint
- resin
- coating composition
- 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
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- Paints Or Removers (AREA)
- Preventing Corrosion Or Incrustation Of Metals (AREA)
Description
【発明の詳細な説明】
本発明は鉄、アルミニウム,マグネシウムの塗
装品を相対湿度約60〜95%下で使用した場合によ
く発生する糸状腐食を抑制する塗料組成物に関す
るものである。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a coating composition that inhibits filiform corrosion that often occurs when coated iron, aluminum, and magnesium articles are used at relative humidity of about 60 to 95%.
糸状腐食は容器,家具,電気製品,自動車など
の塗装品における腐食形態の代表的なものの一つ
であり、この腐食を抑制するための努力が続けら
れている。現在実用されている方法には、鋼板表
面にリン酸鉄やリン酸亜鉛を結晶せしめる、いわ
ゆる化成処理を行ない、この上に塗装を行なう方
法、および鋼板表面を糸状腐食を生じない金属、
即ち亜鉛、ニツケルクロムなどでメツキし、この
上に塗装する方法がある。しかしながら、前者は
乾燥した室内のようなおだやかな使用においては
効果があるが高湿度下での使用では糸状腐食を十
分抑制することはできない。また後者は十分厚い
メツキをすれば糸状腐食を防止することが可能で
はあるが、省資源、製造コストの面で問題であ
り、塗装下地として一般的に用いられるまでには
至つていない。 Filiform corrosion is one of the typical forms of corrosion in painted products such as containers, furniture, electrical appliances, and automobiles, and efforts are being made to suppress this corrosion. Methods currently in use include a method in which a so-called chemical conversion treatment is performed to crystallize iron phosphate or zinc phosphate on the surface of a steel sheet, and then painting is applied, and a method in which the surface of the steel sheet is coated with a metal that does not cause filiform corrosion.
That is, there is a method of plating with zinc, nickel chrome, etc., and then painting on top of this. However, although the former is effective when used in a mild environment such as in a dry room, it cannot sufficiently suppress filiform corrosion when used under high humidity. Although the latter can prevent filiform corrosion by plating sufficiently thickly, it poses problems in terms of resource conservation and manufacturing costs, and has not yet been commonly used as a paint base.
本発明は、この様な実情にかんがみ、塗料に安
価な添加剤を加えることによつて糸状腐食を抑制
することができれば省資源、低コストで塗装製品
の商品価値を向上させ得るきわめて有効な手段に
なると考え種々検討した結果生まれたものであ
る。 In view of these circumstances, the present invention proposes that if filiform corrosion can be suppressed by adding inexpensive additives to paints, it will be an extremely effective means to save resources and improve the commercial value of coated products at low cost. This was the result of various considerations.
即ち、本発明は、糸状腐食を抑制することがで
きる塗料促制物を提供しようとするものである。 That is, the present invention aims to provide a paint promoter that can suppress filiform corrosion.
本発明の塗料組成物は、樹脂を含む塗膜形成成
分と、該塗膜形成成分00重量部に対し、0.5〜20
重量部のハイドロタルサイトを含むことを特徴と
するものである。 The coating composition of the present invention contains a coating film-forming component containing a resin, and 0.5 to 20 parts by weight of the coating film-forming component, based on 0.00 parts by weight of the coating film-forming component.
It is characterized by containing part by weight of hydrotalcite.
本発明によれば、糸状腐食を抑制することがで
きる優れた塗料組成物を提供することができる。
また、この塗料組成物は、後述する塩水噴霧試験
に対しても優れた効果を有し、更に塗膜表面の滑
らかさを損うおそれがない。 According to the present invention, it is possible to provide an excellent coating composition that can suppress filiform corrosion.
Furthermore, this coating composition has excellent effects in the salt spray test described below, and there is no risk of impairing the smoothness of the coating film surface.
次に、本発明にかかる塗料組成物が、この様な
糸状腐食進行を阻止する理由は次のように考えら
れる。即ち、本発明の塗料組成物に含まれるハイ
ドロタルサイトは、糸状腐食の直接原因と考えら
れている糸状腐食の先端に存在する酸と反応し、
糸状腐食先端の酸性を継続的に中和する。しかし
て、ハイドロタルサイトのもつ陰イオン交換能に
より、糸状腐食の進行に触媒的役割を果たしてい
ると考えられている1価の無機陰イオンを捕促
し、糸状腐食先端を移動する1価の無機イオンを
固定化する。 Next, the reason why the coating composition according to the present invention inhibits the progress of such filiform corrosion is considered as follows. That is, the hydrotalcite contained in the coating composition of the present invention reacts with the acid present at the tip of filamentous corrosion, which is considered to be the direct cause of filamentous corrosion.
Continuously neutralizes the acidity of filamentous corrosion tips. Therefore, the anion exchange ability of hydrotalcite traps monovalent inorganic anions, which are thought to play a catalytic role in the progression of filamentous corrosion. Immobilize ions.
本発明において、ハイドロタルサイトの配合割
合は、塗膜形成成分100重量部に対すし0.5〜2重
量部である。0.5重量部に満たない場合には耐糸
状腐食防止の効果が薄く、また20重量部をこえて
配合しても以上の効果が期待できない。より好ま
しい範囲は、塗膜形成成分100重量部に対し1〜
10重量部である。 In the present invention, the blending ratio of hydrotalcite is 0.5 to 2 parts by weight per 100 parts by weight of the coating film forming components. If the amount is less than 0.5 parts by weight, the effect of preventing filamentous corrosion will be weak, and if it exceeds 20 parts by weight, no further effect can be expected. A more preferable range is 1 to 100 parts by weight of the coating film forming component.
It is 10 parts by weight.
また、本発明に用いるハイドロタルサイトは、
Mg,Alの複塩であり、化学式で
Mg4Al2(OH)12CO3・3H2O,Mg6Al2
(OH)16CO3・5H2O又はMg6Al4(CH)16CO3・
4H2Oで表わされるものであり、合成物あるいは
天然物のどちらでも良い。なお、ハイドロタルサ
イトの粒度は均一に分散し、かつ塗装品の表面の
平滑性を得るために、1μm以下であることが好ま
しい。 Furthermore, the hydrotalcite used in the present invention is
It is a double salt of Mg and Al, and its chemical formula is Mg 4 Al 2 (OH) 12 CO 3・3H 2 O, Mg 6 Al 2
(OH) 16 CO 3・5H 2 O or Mg 6 Al 4 (CH) 16 CO 3・
It is represented by 4H 2 O and can be either a synthetic or natural product. The particle size of the hydrotalcite is preferably 1 μm or less in order to be uniformly dispersed and to obtain a smooth surface of the coated product.
塗膜形成成分は、従来の塗膜形成成分をそのま
ま利用できる。例えば、塗料用樹脂,顔料,染
料,充填剤,種々の添加剤が塗膜形成成分とな
る。塗料用樹脂としては、アミノアルキツド樹
脂,焼付け型アクリル樹脂,常乾型アクリル樹
脂,ボイル油,フエノール樹脂,油変性ブタジエ
ン樹脂,エポキシ樹脂等が挙げられる。また、塗
料形態としては粉体,油性,水溶性,電着のいず
れでもよい。なお、本発明の塗料組成物は、金属
製品表面に直接塗布されて効果を発揮するもので
ある。従つて、塗り、中塗り、上塗りと多層に塗
膜が形成される場合には、下塗り塗料用として用
いる。 As the coating film forming component, conventional coating film forming components can be used as they are. For example, paint film-forming components include paint resins, pigments, dyes, fillers, and various additives. Examples of resins for coatings include amino alkyd resins, baking-type acrylic resins, air-drying acrylic resins, boiled oil, phenolic resins, oil-modified butadiene resins, and epoxy resins. The form of the coating may be powder, oil-based, water-soluble, or electrodeposited. The coating composition of the present invention is effective when applied directly to the surface of a metal product. Therefore, when a multilayer coating including coating, intermediate coating, and top coating is formed, it is used as an undercoat paint.
本発明の塗料組成物を塗装する金属製品は、糸
状腐食の発生する。鉄、アルミニウム,マグネシ
ウムの金属製品である。これらの中でも実用上重
要なのは鉄鋼製品である。これらの金属製品は通
常使用される洗浄処理された表面に本発明の塗料
組成物を被覆することができる。なお、塗装前処
理として従来から用いられている。リン酸鉄やリ
ン酸亜鉛を金属表面に結晶させた、いわゆる化成
処理を行なつた金属製品に本発明の塗料組成物を
被覆する場合には糸状腐食防止効果が一層顕著に
なる。 Metal products coated with the coating composition of the present invention undergo filiform corrosion. It is a metal product made of iron, aluminum, and magnesium. Among these, iron and steel products are of practical importance. These metal products can be coated with the coating composition of the present invention on surfaces that have been normally cleaned. Note that it has been conventionally used as a pre-painting treatment. When the coating composition of the present invention is coated on a metal product that has been subjected to a so-called chemical conversion treatment in which iron phosphate or zinc phosphate is crystallized on the metal surface, the effect of preventing filiform corrosion becomes even more remarkable.
以下実施例を記述するが、その前に糸状腐食の
試験法について述べる。 Examples will be described below, but first a test method for filamentous corrosion will be described.
糸状腐食は塗装品の屋外使用においても認めら
れる場合があるが、典型的な形態が見られるのは
屋内使用においてである。このため耐糸状腐食性
の評価は塗装品を屋内に放置して評価するのが最
も実際的である。しかしながら、この試験では結
果が出るまでに時間がかかるために、糸状腐食評
価法としてASTMD−2803がある。この試験法
は塩水噴霧試験(JISZ−2371)を4〜24時間行
なつた後、温度25℃、相対湿度85%の環境で暴露
する方法である。本発明に用いた評価法はこの
ASTMの方法に準拠するもので、塗装板の塗膜
に金属板に達する切傷を付け、この傷部に5%塩
化ナトリウム水溶液を間欠で接触させた後40℃、
相対湿度85%の環境で暴露し、傷部から発生する
糸状腐食の最大長さ5本を選び、その平均値から
評価するものである。 Although filiform corrosion may be observed when painted products are used outdoors, its typical form is observed when used indoors. For this reason, it is most practical to evaluate the filamentous corrosion resistance by leaving the painted product indoors. However, since this test takes time to produce results, ASTMD-2803 is available as a filamentous corrosion evaluation method. This test method involves conducting a salt spray test (JISZ-2371) for 4 to 24 hours, and then exposing the product to an environment at a temperature of 25°C and a relative humidity of 85%. The evaluation method used in the present invention is this
This method complies with the ASTM method, where a cut is made in the paint film of a painted board that reaches the metal plate, and after intermittently contacting the cut with a 5% aqueous sodium chloride solution, the coating is heated at 40°C.
Five maximum lengths of thread-like corrosion generated from scratches are selected after exposure in an environment with relative humidity of 85%, and the evaluation is based on the average value.
実施例 1
アミノアルキツド塗料にハイドロタルサイトを
添加して塗料組成物を調整し、次いで、リン酸亜
鉛処理を施した鋼板にこの塗料組成物を塗装し、
得られた塗装板の表面の糸状腐食状態を観察し
た。Example 1 A paint composition was prepared by adding hydrotalcite to an aminoalkyd paint, and then this paint composition was applied to a steel plate treated with zinc phosphate,
The state of filamentous corrosion on the surface of the obtained coated plate was observed.
すなわち、粒径約0.5μmのハイドロタルサイト
を20倍量のキシレンを主成分とする塗料用シンナ
ーに超音波を用いて均一に分散させ、これを市販
のアミノアルキツド塗料に塗膜形成成分に対しハ
イドロタルサイトの添加量が3重量%になるよう
に添加した。次いでシンナーによりスプレー塗装
に適した粘度に調整し、あらかじめリン酸亜鉛処
理をした厚み0.8mmの鋼板(付着量1.5g/m2)に
乾燥膜厚で約30μmになるようにスプレー塗装し、
140℃で30分間焼付けを行なつた。得られた塗装
板を前述の糸状腐食試験に供した。なお、比較の
ため、ハイドロタルサイトは含まない前記と同様
の塗料を調製し、同様に塗装し焼付けかつ糸状腐
食試験もした。 That is, hydrotalcite with a particle size of approximately 0.5 μm is uniformly dispersed in 20 times the amount of paint thinner whose main component is xylene using ultrasonic waves, and this is added to a commercially available amino alkyd paint by applying hydrogel to the film-forming components. Talcite was added in an amount of 3% by weight. Next, the viscosity was adjusted with thinner to a level suitable for spray painting, and spray painting was applied to a 0.8 mm thick steel plate (coating amount: 1.5 g/m 2 ) that had been previously treated with zinc phosphate to a dry film thickness of approximately 30 μm.
Baking was performed at 140°C for 30 minutes. The obtained coated plate was subjected to the filamentous corrosion test described above. For comparison, a paint similar to the above without containing hydrotalcite was prepared, painted and baked in the same manner, and a filiform corrosion test was also conducted.
第1図に示すごとく、糸状腐食はハイドロタル
サイトを添加しない塗料の塗装板Aにおいて、
6.2mmになつた時点で、ハイドロタルサイトを3
重量%添加した塗料の塗装板Bは2.4mm以下であ
つた。 As shown in Figure 1, filamentous corrosion occurs on plate A coated with paint that does not contain hydrotalcite.
When it reaches 6.2mm, add 3 hydrotalcites.
The coated plate B of the paint to which % by weight was added was 2.4 mm or less.
実施例 2
実施例1で調製したのと同じ塗料組成のアミノ
アルキツド塗料を用い、リン酸亜鉛処理が施こさ
れていない厚み0.8mmの鋼板に乾燥膜厚べ約30μm
になるようにスプレー塗装し、140℃で30分間焼
付けを行なつた。得られた塗装板を前述の糸状腐
食試験に供した。同様にハイドロタルサイトは含
まない塗料を用いた塗装板を作り、糸状腐食試験
をした。Example 2 Using an aminoalkyd paint with the same paint composition as that prepared in Example 1, a dry film thickness of approximately 30 μm was applied to a 0.8 mm thick steel plate that had not been subjected to zinc phosphate treatment.
It was spray painted and baked at 140℃ for 30 minutes. The obtained coated plate was subjected to the filamentous corrosion test described above. Similarly, a painted board was made using a paint that did not contain hydrotalcite, and a filiform corrosion test was conducted.
第2図に示すごとく、糸状腐食は、ハイドロタ
ルサイトを含まない塗装板Cにおいて6.0mmにな
つた時点で、上記本発明にかかる塗料組成物で調
製された塗装板Dの糸状腐食は4.1mmであつた。 As shown in FIG. 2, when the filamentous corrosion reached 6.0 mm on coated plate C which does not contain hydrotalcite, the filamentous corrosion on coated plate D prepared with the coating composition according to the present invention reached 4.1 mm. It was hot.
実施例 3
アニオン型電着塗料に前記実施例1および2で
用いたと同様のハイドロタルサイトを添加した塗
料組成物を調整し、このものをリン酸亜鉛処理を
施した鋼板に塗装し、得られた塗装板の糸状腐食
を観察した。Example 3 A coating composition was prepared by adding the same hydrotalcite as used in Examples 1 and 2 to an anionic electrodeposition coating, and this composition was applied to a steel plate treated with zinc phosphate. Filamentous corrosion was observed on the painted plate.
すなわち、市販のアニオン型電着塗料(神東塗
料株式会社製、商品名スーパーアニオン)に塗膜
形成成分に対し前記ハイドロタルサイトを3重量
%および6重量%添加した2種類の塗料組成分を
用意した。 That is, two types of paint compositions were added to a commercially available anionic electrodeposition paint (manufactured by Shinto Paint Co., Ltd., trade name: Super Anion), in which 3% and 6% by weight of the hydrotalcite were added to the film-forming components. Prepared.
次に、前記実施例1と同様のリン酸亜鉛処理を
施した鋼板に乾燥膜圧20μmになるよう電着塗装
をし、170℃で30分間焼付けを行なつた。得られ
た塗装板を前記の糸状腐食試験に供した。 Next, a steel plate treated with zinc phosphate in the same manner as in Example 1 was electrodeposited to a dry film thickness of 20 μm, and baked at 170° C. for 30 minutes. The obtained coated plate was subjected to the filamentous corrosion test described above.
また、比較のためハイドロタルサイトを含ませ
ない塗料を調整し同様に塗装し焼付けを行ない、
このものの糸状腐食試験を行なつた。 In addition, for comparison, we prepared a paint that did not contain hydrotalcite, painted it in the same way, and baked it.
A filiform corrosion test was conducted on this material.
第3図に示すごとく、ハイドロタルサイトを含
まない塗装板Eの糸状腐食が9.1mmになつた時点
で、ハイドロタルサイト3重量%含有の塗装板F
の糸状腐食は5.3mm、または6重量%含有の塗装
板Gの糸状腐食は2.2mmであつた。 As shown in Figure 3, when the filamentous corrosion of coated plate E that does not contain hydrotalcite reaches 9.1 mm, the coated plate F that contains 3% by weight of hydrotalcite
The thread-like corrosion was 5.3 mm, or the thread-like corrosion of the coated plate G containing 6% by weight was 2.2 mm.
以上実施例より明らかなごとく、本発明に用い
たハイドロタルサイトを樹脂を含む塗膜形成成分
に添加することにより、塗装板の糸状腐食を防止
する効果は顕著である。 As is clear from the examples above, adding the hydrotalcite used in the present invention to a coating film-forming component containing a resin has a remarkable effect of preventing filiform corrosion of painted plates.
また、本発明に用いた塗料組成物は、塩水噴霧
試験に対しても優れた効果を発揮することが分
る。 Furthermore, it can be seen that the coating composition used in the present invention exhibits excellent effects in the salt spray test.
図は本発明の実施例を示し、第1図は実施例
1、第2図は実施例2、第3図は実施例3におけ
る糸状腐食試験の結果を示す図である。
The figures show examples of the present invention; FIG. 1 is a diagram showing the results of a filiform corrosion test in Example 1, FIG. 2 is Example 2, and FIG. 3 is Example 3.
Claims (1)
100重量部に対し0.5〜20重量部のハイドロタルサ
イトを含有することを特徴とする耐糸状腐食性塗
料組成物。 2 樹脂はアミノアルキツド樹脂、アクリル樹
脂、ボイル油、フエノール樹脂、油変性ブタジエ
ン樹脂、エポキシ樹脂、である特許請求の範囲第
1項に記載の塗料組成物。 3 ハイドロタルサイトは、Mg,Alの複塩であ
り、化学式でMg4Al2(OH)12CO3・3H2O,
Mg6Al2(OH)16CO3・5H2O又はMg6Al7
(OH)16CO3・4H2Oである特許請求の範囲第1項
記載の塗料組成物。[Claims] 1. A coating film-forming component containing a resin, and the coating film-forming component
A filamentous corrosion-resistant coating composition characterized by containing 0.5 to 20 parts by weight of hydrotalcite per 100 parts by weight. 2. The coating composition according to claim 1, wherein the resin is an aminoalkyd resin, an acrylic resin, a boiled oil, a phenolic resin, an oil-modified butadiene resin, or an epoxy resin. 3 Hydrotalcite is a double salt of Mg and Al, and its chemical formula is Mg 4 Al 2 (OH) 12 CO 3・3H 2 O,
Mg 6 Al 2 (OH) 16 CO 3・5H 2 O or Mg 6 Al 7
The coating composition according to claim 1, which is (OH) 16 CO 3 .4H 2 O.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP3992483A JPS59166568A (en) | 1983-03-10 | 1983-03-10 | Coating compound composition having thready corrosion resistance |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP3992483A JPS59166568A (en) | 1983-03-10 | 1983-03-10 | Coating compound composition having thready corrosion resistance |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS59166568A JPS59166568A (en) | 1984-09-19 |
| JPH0442434B2 true JPH0442434B2 (en) | 1992-07-13 |
Family
ID=12566478
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP3992483A Granted JPS59166568A (en) | 1983-03-10 | 1983-03-10 | Coating compound composition having thready corrosion resistance |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS59166568A (en) |
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH03128903A (en) * | 1989-07-13 | 1991-05-31 | Fine Kurei:Kk | Method for modifying synthetic resin and modified synthetic resin |
| JP2000191943A (en) * | 1998-10-19 | 2000-07-11 | Nts:Kk | Film-forming composition and its production |
| DE60001127T2 (en) | 1999-07-14 | 2003-07-17 | N.T.S. Corp., Suwa | Layer-forming composition and method of manufacture |
| JP2001131490A (en) * | 1999-11-04 | 2001-05-15 | Kansai Paint Co Ltd | Matte anionic electrodeposition coating |
| JP2001302944A (en) * | 2000-04-25 | 2001-10-31 | Nts:Kk | Coating-film-forming composition, its production method, and coating film |
| GB0212633D0 (en) * | 2002-05-31 | 2002-07-10 | Uws Ventures Ltd | Anti-corrosion pigments |
| US7745010B2 (en) * | 2005-08-26 | 2010-06-29 | Prc Desoto International, Inc. | Coating compositions exhibiting corrosion resistance properties, related coated substrates, and methods |
| US8231970B2 (en) * | 2005-08-26 | 2012-07-31 | Ppg Industries Ohio, Inc | Coating compositions exhibiting corrosion resistance properties and related coated substrates |
| TW202503083A (en) * | 2023-07-14 | 2025-01-16 | 日商日本製鐵股份有限公司 | Surface treated steel |
-
1983
- 1983-03-10 JP JP3992483A patent/JPS59166568A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS59166568A (en) | 1984-09-19 |
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