JPS5896876A - Formation of wear and corrosion resistant film on metallic material - Google Patents

Formation of wear and corrosion resistant film on metallic material

Info

Publication number
JPS5896876A
JPS5896876A JP19412481A JP19412481A JPS5896876A JP S5896876 A JPS5896876 A JP S5896876A JP 19412481 A JP19412481 A JP 19412481A JP 19412481 A JP19412481 A JP 19412481A JP S5896876 A JPS5896876 A JP S5896876A
Authority
JP
Japan
Prior art keywords
alkali metal
film
aqueous solution
silicate
coating
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.)
Granted
Application number
JP19412481A
Other languages
Japanese (ja)
Other versions
JPS6214029B2 (en
Inventor
Hidekimi Kadokura
秀公 門倉
Yoshinori Furuumi
古海 好則
Tetsuo Fujita
藤田 哲夫
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.)
Sumitomo Chemical Co Ltd
Original Assignee
Sumitomo Chemical Co Ltd
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 Sumitomo Chemical Co Ltd filed Critical Sumitomo Chemical Co Ltd
Priority to JP19412481A priority Critical patent/JPS5896876A/en
Publication of JPS5896876A publication Critical patent/JPS5896876A/en
Publication of JPS6214029B2 publication Critical patent/JPS6214029B2/ja
Granted legal-status Critical Current

Links

Abstract

PURPOSE:To form a film with superior resistance to water, moisture, wear and corrosion by applying an aqueous soln. of an alkali metallic silicate having a specified composition contg. optionally boric acid or multivalent metallic ions to the surface of a metallic material and by baking the applied soln. CONSTITUTION:An aqueous soln. of an alkali metallic silicate represented by the formaul (where R is Na or K, 0.1<=3 and 4<=n<10) is used as a practical film forming agent. Boric acid and/or multivalent metallic ions may be dissolved in the soln. The film forming agent is applied to a part or the whole of the surface of a metallic material, dried and baked at >= about 150 deg.C. Thus, a transparent hard film with superior water resistance, corrosion resistance and airtightness can be formed.

Description

【発明の詳細な説明】 本斃明は金属材料への耐磨耗性、耐蝕性被膜の形成方法
に関するものである。更に詳細には特定組成のアルカリ
金鷹ケイ酸#1を金属材料に塗布、焼付けすることによ
る金属材料への耐磨耗性、耐蝕性被膜の形成方法に関す
るものである。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for forming a wear-resistant and corrosion-resistant coating on metal materials. More specifically, the present invention relates to a method of forming an abrasion-resistant and corrosion-resistant coating on a metal material by applying and baking alkali gold silicic acid #1 having a specific composition onto the metal material.

金属材料面にアルカリ金属ケイ酸塩を塗布し乾燥するこ
とにより、硬膏の高い透明な被膜が形成できるととけ公
知である。
It is known that a highly transparent coating of plaster can be formed by applying an alkali metal silicate to a metal surface and drying it.

しかしながら、ケイ酸カリウムやケイ酸ナトリウムから
形成される被膜の場合には、耐湿性が悪く、空気中の炭
酸ガスや亜′5It酸ガスと反応し5表面が白華すると
いう問題があり、且つ、耐水性が劣る為、水の作用する
場所での使用ができ危いという問題点を有している。
However, in the case of coatings formed from potassium silicate or sodium silicate, there are problems such as poor moisture resistance, reaction with carbon dioxide gas and '5Itite acid gas in the air, and efflorescence of the surface. However, since it has poor water resistance, it is dangerous to use it in places exposed to water.

アルカリ金属ケイ酸塩より擾る被膜の耐湿性、耐水性を
肉止させる方法として、アルカリ4禍ケイFJJ!iの
被膜を亜硫駿ガス、炭酸ガス、および二酸化チッ素から
なる群から選ばれた少ガくとも7つのガスを含む湿気に
富んだ雰囲気中に放置した後、水洗する方法が提案され
ている(特開昭13−413144!号公報)6#方法
によれば、il+水性の向上は期待できるものの、工穆
が豪艙となるとか被覆されていない部分の金属材料が、
酸性ガスおよび水により腐食されるとか、11性ガスに
よるアルカリ分の中和が不充分な場合は、水洗時に被膜
が失透し、且つ、酸性ガスによ如ガラス質皮膜中のアル
カリを必要量中和する仁とは困難であ勢、長時間を要す
る郷の問題点を有している。
As a method to improve the moisture resistance and water resistance of a film that has deteriorated from alkali metal silicate, Alkali 4-Magkei FJJ! A method has been proposed in which the film of i is left in a humid atmosphere containing at least seven gases selected from the group consisting of sulfurous gas, carbon dioxide, and nitrogen dioxide, and then washed with water. According to the 6# method (Japanese Unexamined Patent Publication No. 13-413144!), an improvement in IL+aqueous property can be expected;
If the film is corroded by acid gas and water, or if the alkali content is insufficiently neutralized by the 11-group gas, the film will devitrify when washed with water, and the acid gas will remove the necessary amount of alkali from the vitreous film. Neutralizing the enemy is difficult and difficult, and has problems that require a long time.

また、アルカリ金属ケイ酸塩に耐水性、耐湿性を付与す
る方法として、リチウムを含む溶合アルカリ金属のケイ
酸塩も提案されている(%公昭J ?−/Jj、24号
公報、%開昭30− AIJJ1号公@)、シかし、皺
方汁のいずれの場合にも被覆組放物の過用は常温硬化用
であり、金属材性、耐酸化性に劣るという欠点を有して
いる。
In addition, as a method of imparting water resistance and moisture resistance to alkali metal silicates, fused alkali metal silicates containing lithium have been proposed (%Kosho J?-/Jj, No. 24, 1963 - AIJJ No. 1 @), overuse of coating assemblies is used for curing at room temperature, and has the disadvantage of poor metal properties and oxidation resistance in both cases of staining and wrinkling. ing.

かかる観点に立脚して、本発明者らは、全項材料に耐摩
耗性、1鶴性等を付与すゐ方法を開発すぺ〈鋭意研究を
行かった結果、金属材料に特性、耐蝕性輯を付与できる
ことを見い出し、本発明を完成するに至った。
Based on this viewpoint, the present inventors have developed a method for imparting wear resistance, corrosion resistance, etc. to all materials. The present invention was completed based on the discovery that it is possible to impart a degree of flexibility.

すなわち、本発明は金属材料の−it六は全部の面に一
般式 %式%) で表わされるアルカリ金属ケイ1m?塩の水溶液または
該アルカリ金属ケイ酸塩の水溶澄参キ椿棲−1(*つ酸
および /lたけ多価金属イオンを溶解してびる水溶沿蝕性被膜
の形成方法を提供するにある。
That is, in the present invention, -it6 of the metal material is expressed by the general formula %) on all surfaces of the alkali metal silicon 1m? An object of the present invention is to provide a method for forming a water-soluble corrosive coating by dissolving an aqueous solution of a salt or an aqueous solution of the alkali metal silicate.

本発明方法の実施に肖り、被膜形成剤としては一般式 %式% (式中、累、mおよびnは前記と同じ、)で表わされる
アルカリ金属ケイ酸塩の水溶液または訪アルカリ金属ケ
イ酸塩の水溶液に水つ酸および/まtけ多価金属イオン
を溶解して成る水溶液が用いられる。
In carrying out the method of the present invention, the film forming agent may be an aqueous solution of an alkali metal silicate or an alkali metal silicate represented by the general formula % (wherein, cumulative, m and n are the same as above). An aqueous solution prepared by dissolving hydroxide and/or polyvalent metal ions in an aqueous salt solution is used.

本発明方法において、リチウムを含むアルカリ金属ケイ
酸塩を用いる理由は前述の一般式%式% (式中、R,rnおよびnは前言己と同じ。)で表わさ
れるアルカリ金属ケイ酸塩において、nを大吉<シ、そ
の効果によりアルカリ金属ケイ酸塩の耐水性を向上させ
ようとするにある。
In the method of the present invention, the reason for using an alkali metal silicate containing lithium is that in the alkali metal silicate represented by the general formula % (wherein R, rn, and n are the same as above), The purpose of this study is to improve the water resistance of alkali metal silicates by utilizing the effect of n.

すなわち、ナトリウムやカリウムのケイシ塩は一般式%
式%”081%で示されるものであや、nが大きい程耐
水性は向上するが、nが9以上と麿ると水溶液の状態を
維持で1畳庁り、被験形成剤としての用をなさない亀の
となるが、Li2Q成分を含ませることにより、nを任
意に変化させても水溶液の状態を維持できるものとがる
ことを利用したものである。一般式中のn1tjtも重
要な構成要件とがるものであり、q≦n(/θ好fL<
は!≦n≦tとされる。nが9未満となると、形成した
被膜の耐水性が低下するように痩り、空気中に放置して
おくと白亜化し、沸騰水棒に浸漬すると失透する尋の不
側合を生じるようになるし、一方/p以上になるとll
Es性が低下し被膜にクラックが人!ll、l < &
Zという不都合を生じるようになり好オしくない。
In other words, siliceous salts of sodium and potassium have the general formula %
It is expressed by the formula %"081%, and the larger n is, the better the water resistance is, but if n is 9 or more, it will remain in an aqueous solution state and become useless as a test forming agent. Although it is not a turtle, it takes advantage of the fact that by including the Li2Q component, the state of an aqueous solution can be maintained even if n is arbitrarily changed. n1tjt in the general formula is also an important component. The requirements are sharp, and q≦n(/θfL<
teeth! ≦n≦t. If n is less than 9, the water resistance of the formed film will decrease, and if left in the air it will become chalky, and if immersed in a boiling water stick, it will devitrify and cause side agglutination. On the other hand, when it becomes /p or more, ll
The Es property decreases and cracks appear in the coating! ll, l <&
This is not desirable as it causes the inconvenience of Z.

ナた、mは通常θ、/≦III<J、好オしくけ0、−
≦m≦−0(/とされ為0mが□、/未満となると、n
が大きい時の水llI液の安宏性が悪くたったり、被膜
にクラックが入り易くカり好ましくきいし、一方1が3
以上に麿ると耐水性が劣るように庁るので#0fff<
麿い。
Nata, m is usually θ, /≦III<J, preferably 0, -
≦m≦-0 (/, so if 0m becomes less than □, /, then n
When the water is large, the stability of the water lllI solution is poor, and the film tends to crack and is undesirable.
If it is longer than that, the water resistance will be inferior, so #0fff<
Fast.

本発明方法のアルカリ金属ケイ酸塩の一般式において、
Rはカリ9ムまたはナトリウムを示すものであ勢、これ
らけ賑独tたは混合物としても使用することがで1名。
In the general formula of the alkali metal silicate of the method of the present invention,
R stands for potassium or sodium, and it can also be used as a combination or as a mixture.

このようなアルカリ金属ケイ#塩水溶液の製造方法は公
知の方法を適用することかで1!−1例えば水酸化リチ
ウム、水酸化ナトリウム、水酸化カリウム、二酸化ケイ
素の混合物を加熱して製造することもできるし、ケイ酸
リチウムに水酸化す)Lllラム水酸化カリウムをil
!解させて製造することもできるが、通常は市販のケイ
酸リチウム水溶液とケイ酸ナトリウム水g沿または/お
よびケイ酸カリウム水m液を混合することで製造できゐ
、得られたアルカリ金属ケイ酸塩の水溶液は被膜欠陥の
原因とまる固体分を除く為、−過した後使用するのが好
ましい。
Such an alkali metal silica #salt aqueous solution can be produced by applying a known method! -1 For example, it can be produced by heating a mixture of lithium hydroxide, sodium hydroxide, potassium hydroxide, and silicon dioxide, or it can be hydrated to lithium silicate).
! Although it can be produced by mixing a commercially available lithium silicate aqueous solution with a sodium silicate solution and/or a potassium silicate solution, the resulting alkali metal silicate It is preferable to use the aqueous salt solution after it has been filtered in order to remove solids that may cause coating defects.

本発明方法で使用されるアルカリ金属ケイ酸塩は焼付に
より耐水性を有する透明被膜を形成するものであるが、
上述せゐアルカリ金属ケイ酸塩水溶液に水つ酸および/
lたけ多価金属イオンを含ませるととによね、更に耐水
性を向上させることができる。多価余興イオンと1.、
ては亜鉛、アルミニウム郷のイオンを磁げることができ
、このようなホウ酸および/′fたは多価金属イオンを
含着せることで、nが小さい場合の耐水性を向上するこ
とが可能となる。
The alkali metal silicate used in the method of the present invention forms a transparent film with water resistance by baking.
Hydroxic acid and/or
The water resistance can be further improved by including 1 more polyvalent metal ions. Multivalent entertainment ion and 1. ,
It is possible to magnetize zinc and aluminum ions, and by impregnating such boric acid and /'f or polyvalent metal ions, it is possible to improve water resistance when n is small. becomes.

*つPおよび7寸たは多価全綱イオンを含有させ為方法
としては、ホウ*、、*つ砂、*つ醗カリウムのような
アルカリ余興*つWI塩や亜鉛。
Methods for containing *P and 7 or polyvalent ion include borium*, *tsusa, *tsutsuzumi*tsuWI salt such as potassium, and zinc.

アル鳳ニウム等の多価全域の際化物、水酸化物、ケイ酸
塩、ケイフッ化物等を予めアルカリ金属ケイ酸塩の単独
の水溶液に溶解させてシ〈か、!!たは本発明のアルカ
リ金属ケイ酸塩に直接溶解させゐ方法を採ることもでき
る。承つ酸および/lたけ多偵金属イオンの量は酸化物
として乾燥被膜中に約/〜j重量%、好ましくは/〜3
重量係存在するように添加される。多価金属化合物等の
溶解残漬け、通常−過により除去さ触性被膜の形成方法
において、被膜の膜厚は約ρ、7〜−μm、好ましくは
θ、、!〜八コよとへれる。
A wide range of polyvalent compounds such as aluminum, hydroxides, silicates, fluorosilicides, etc. are dissolved in advance in a single aqueous solution of alkali metal silicate, and... ! Alternatively, a method of directly dissolving it in the alkali metal silicate of the present invention can be adopted. The amount of acid and metal ions present in the dry film as oxides is about /~J% by weight, preferably /~3% by weight.
Added in proportion to weight. In the method of forming a tactile film that is removed by dipping a polyvalent metal compound, etc., or removing it by filtration, the film thickness of the film is about ρ, 7 to - μm, preferably θ, ! ~Hachikoyoto Hereru.

膜厚がθ、/顯未満と々ると、実質的に保■効果が期待
しに〈〈々るし、一方、−μmを超えると焼付は時に被
膜にふくれを生じたり、クラックを生じたり、更には密
着性が低下するようにな委好ましくtい、このs斤膜厚
にaWする為に、本発明のアルカリ金属ケイ酸塩は水に
より通常固型分濃度を約1〜36重量−となるように製
置調整して用いるのが好オしい。
If the film thickness is less than θ,/μm, the protective effect will not be expected, but if it exceeds -μm, the film may swell or crack. In order to reduce the film thickness, the alkali metal silicate of the present invention is usually reduced in solid content to about 1 to 36% by weight with water. It is preferable to adjust the manufacturing location so that

本発明方法のアルカリ金属ケイ酸塩の水溶液にエチレン
グリコール、グリセリン郷の乾燥遅延剤を添加混合し、
作業性の改善をはかることができる。これらの乾燥遅延
剤の添加置け、焼成後の残留炭素による着色を考慮して
、一般にアルカリ金属ケイ酸塩の水溶液に対して一5重
量憾以下量添加される。
Adding and mixing ethylene glycol and a drying retardant of glycerin to the aqueous solution of the alkali metal silicate of the method of the present invention,
Workability can be improved. In consideration of the addition of these drying retarders and the coloration caused by residual carbon after firing, they are generally added in an amount of 15% or less by weight to the aqueous solution of the alkali metal silicate.

本発明方法の実施に当り、金属材料は前述のアルカリ金
属ケイ酸塩が塗布され、次いで乾燥、焼付が行々われる
。金属材料へのアルカリ金^ケイ酸塩の塗布に際し金F
7!4材料は予め脱脂しておくことが好ましく、脱脂が
不充分子:場合は均一な被膜が得られず、被膜の欠陥の
原因とがる。
In carrying out the method of the present invention, the metal material is coated with the alkali metal silicate described above, then dried and baked. Gold F when applying alkali gold silicates to metal materials
7!4 It is preferable to degrease the material in advance; if degreasing is insufficient, a uniform coating may not be obtained and this may cause defects in the coating.

金属材料の脱脂方法としては、9!轡、アルカリ脱脂、
酸洗、熱水洗浄、界面活性剤洗浄等公知の方法が利用で
き、金属の特性により任童に選ぶことがで舞る。
9! How to degrease metal materials! Sod, alkaline degreasing,
Known methods such as acid washing, hot water washing, and surfactant washing can be used, and the method can be selected depending on the characteristics of the metal.

更に、本発明方法のアルカリ金属ケイ酸1に界面活性剤
を溶解し1、金属材料との濡れ性を完全なものとするこ
とができる。金属材料への被膜形成側の塗布は、スプレ
ー、ディッピング。
Furthermore, by dissolving a surfactant in the alkali metal silicic acid 1 of the method of the present invention, it is possible to perfect the wettability with the metal material. The film forming side is applied to metal materials by spraying or dipping.

ローラー轡公知の方法から選べば良いが、通常ディッピ
ングによゐ方法が好ましく用いられる。
Although any known method may be selected, a dipping method is usually preferred.

この時均−被膜を祷る為、全綱材料を加熱してシ〈とか
、塗布液を暖めておく等の方法本採用することができる
。塗布された金属材料は乾燥され、次いで焼付けされる
。焼付は温度は高温程緻密で耐水性の被膜が得られるが
、耐水性からは約/jθ℃以上が好ましい、上限は特に
限定されるものではないが、コス)、金属の材質等から
通常jj0°Ctでの温度が用いられる。
In order to achieve this uniform coating, methods such as heating the entire steel material or warming the coating solution can be employed. The applied metal material is dried and then baked. The higher the baking temperature, the more dense and water-resistant the coating will be obtained, but from the viewpoint of water resistance, it is preferable to bake at a temperature of about /jθ°C or higher.The upper limit is not particularly limited, but it is usually jj0 Temperatures in °Ct are used.

〈ない、公知の方法の場合は耐水性は付与プれるとして
も、公知の組成物を金属材料に塗布し、焼付は硬化した
場合は亀裂、剥離を生じ、実質的に金属材料を保−する
ことができない。
(No, in the case of known methods, water resistance may be imparted, but if a known composition is applied to a metal material and baked, cracks and peeling occur when hardened, and the metal material is substantially preserved.) I can't.

このようにして得られる本発明方法による誉膜は透明で
あり、且つ耐水性、耐食性、気密性に優れ、更にはシラ
力質の高い硬変を有している為、金属の防食、酸化防止
、傷つき防止等に優れた効果を発揮するものでああ、被
覆される金属材料としては、アルカリ金属ケイ酸塩によ
り被膜形成可能なものなら何でも良く、例えばアルミニ
ウム、鋼、鉄、貴金属轡およびこれら肝性、よごれ防止
性、傷つき防止性等を付与することがで11鋼および銅
合金等酸化され易い金属に酸化防止性を付与することが
できる。また、電気絶縁性を付与することも可能である
The film thus obtained by the method of the present invention is transparent, has excellent water resistance, corrosion resistance, and airtightness, and has high hardness, so it can be used to prevent metal corrosion and oxidation. The metal material to be coated may be any material that can form a film with alkali metal silicate, such as aluminum, steel, iron, precious metals, and other metal materials. By imparting anti-oxidation properties, anti-fouling properties, anti-scratch properties, etc., it is possible to impart anti-oxidation properties to metals that are easily oxidized, such as No. 11 steel and copper alloys. It is also possible to provide electrical insulation.

勿論このような被膜は金概単体に限らず、メッキ面や蒸
着面に対しても膚効であり、熱交換器用金寓材料、熱反
射e光反射用金属材料、装飾材料、更にはメッキ、蒸着
材料の補−等多くの用途に使用できる。
Of course, such a coating is effective not only on metal itself, but also on plated and vapor-deposited surfaces, and is useful for metal materials for heat exchangers, metal materials for heat and light reflection, decorative materials, and even plating, It can be used for many purposes such as supplementing vapor deposition materials.

以下に実施例により本発明を更に群細に説明するが、本
発明はこれらによって制限されるものでけがい。
The present invention will be explained in more detail with reference to examples below, but the present invention is not limited by these examples.

々お、実施例中の部および嗟は重量基準を示す。In the examples, parts and numbers are based on weight.

実施例中の物性測定は以下の方法に依った。The physical properties in the examples were measured by the following method.

/)外  1! :目視により透明性、発泡、クラッタ
を観察した。
/) Outside 1! : Visually observed transparency, foaming, and clutter.

−)耐水 性:沸騰水中で所定時間煮沸した後の被膜を
観察した。
-) Water resistance: The film was observed after being boiled in boiling water for a predetermined period of time.

J)1醗化性:所定温暖で所定時間φ成した後、表面観
察を行1に−)た。
J) 1-oxidation property: After φ was incubated at a predetermined temperature for a predetermined time, the surface was observed in line 1-).

q)膜  厚:表面粗さ針によね、段差測定を観察した
q) Film thickness: Surface roughness was measured using a needle.

実施例/〜ム、比較例7〜ム ケイ醗ソーダ、ケイ酸カリウム、ケイ酸リチウムの水溶
液を所定割合で混合し第1IIに示す組l比Ouチウム
を會むアルカリ金属ケイ酸塩水溶液を得た。この液を一
過し、水によaljI型分/j言量嗟と擾るように希釈
した。
Examples / Comparative Example 7 - Aqueous solutions of sodium chloride, potassium silicate, and lithium silicate were mixed in a predetermined ratio to obtain an alkali metal silicate aqueous solution having a composition ratio of lithium as shown in Part 1II. . This solution was filtered and diluted with water to a volume of 1/2.

この塗布液中に鋼板およびアルミニウム板を70分乾燥
させた稜、更に−jO″Cで7θ分間焼付けた。この被
覆金属材料の物性を第7表に示す。
The edges of the steel plate and aluminum plate were dried in this coating solution for 70 minutes, and then baked at -jO''C for 7θ minutes.Table 7 shows the physical properties of the coated metal materials.

がお被膜厚みは発泡等の異常物を除いていずれも約θ、
j/a!lであった・ 訳・ 1濫1 性、耐蝕性、耐酸化性(銅の場合)が悪く、たとえ被覆
したとしてもnが9未満の場合(比較例3)は耐水性に
劣り、nが10以上(比較例q)となると密着性が劣る
様になり、mが3以上(比較例孟)にがると耐水性が劣
るようになるが、本発明方法に示される範囲を示すこと
が明らかである。
The thickness of the coating is approximately θ, excluding abnormalities such as foaming.
j/a! Copper properties, corrosion resistance, and oxidation resistance (in the case of copper) are poor, and even if coated, if n is less than 9 (Comparative Example 3), water resistance is poor and n is If m is 10 or more (Comparative Example q), the adhesion will be poor, and if m is 3 or more (Comparative Example Meng), the water resistance will be poor. it is obvious.

実施例7 ケイ酸ナトリウム、ケイ酸リチウムを混合し、Naff
1o・θ7Li20 ’ !;、θB 1o、の組故の
固型分:10重量係の被覆液を調合し、この水溶液に一
憾の*つ砂を溶解させた。*つ砂溶解前e後の水溶液を
鋼板に塗布し、−00°Cで70分間の焼付けを行なっ
た。この被覆銅板の物性モル比はNad ”0J7Li
lO’41.4810g ”0./llB2O5であっ
た。
Example 7 Mixing sodium silicate and lithium silicate, Naff
1o・θ7Li20'! A coating solution having a solid content of 10% by weight due to the composition of ;, θB 1o, was prepared, and a small amount of sand was dissolved in this aqueous solution. *The aqueous solution before and after sand dissolution was applied to a steel plate, and baked at -00°C for 70 minutes. The physical property molar ratio of this coated copper plate is Nad “0J7Li
1O'41.4810g"0./11B2O5.

第   λ   表 第1表より*つ醗化合物の添加により耐水性が向上する
ことが明らかである。
It is clear from Table 1 that the water resistance is improved by the addition of the *Tsuzu compound.

Claims (1)

【特許請求の範囲】 /)金属材料の一部または全部の面に一般式%式%) であられされゐアルカリ金属ケイ−塩の水溶液またけ骸
アルカリ金輿ケイ酸塩の水溶液に*つ酸および/lたは
多価金属イ寸ンを溶解して成る水溶液から実質的にeゐ
被膜形成剤−)アルカリ金属ケイ酸塩の一般式において
、mおよびnが、θ8.2≦m≦−0θ、j≦n≦にO
形成方法。 J)ホウ酸がホウ酸またはアルカリ金属ホウ酸塩として
添加され* ”l1QBとして乾燥被膜中に純性、耐蝕
性被膜の形成方法。 41)アルカリ金属ケイ酸塩水溶液の固型分層1がj〜
3θ14伊チであり、該水溶液により得られ石被膜の膜
厚がθ、/〜λμlであゐことをの形成方法。
[Scope of Claims] /) An aqueous solution of an alkali metal silicate coated with the general formula % on a part or all of the surface of the metal material, and an aqueous solution of an alkali metal silicate coated with oxalic acid. and/l or a polyvalent metal component dissolved in an aqueous solution to form a film-forming agent-) In the general formula of an alkali metal silicate, m and n are 0θ, O for j≦n≦
Formation method. J) A method for forming a pure, corrosion-resistant coating in a dry coating in which boric acid is added as boric acid or an alkali metal borate* as a dry coating. 41) A solid fraction layer 1 of an aqueous alkali metal silicate solution is ~
3θ14 times, and the thickness of the stone coating obtained from the aqueous solution is θ,/~λμl.
JP19412481A 1981-12-02 1981-12-02 Formation of wear and corrosion resistant film on metallic material Granted JPS5896876A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP19412481A JPS5896876A (en) 1981-12-02 1981-12-02 Formation of wear and corrosion resistant film on metallic material

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP19412481A JPS5896876A (en) 1981-12-02 1981-12-02 Formation of wear and corrosion resistant film on metallic material

Publications (2)

Publication Number Publication Date
JPS5896876A true JPS5896876A (en) 1983-06-09
JPS6214029B2 JPS6214029B2 (en) 1987-03-31

Family

ID=16319303

Family Applications (1)

Application Number Title Priority Date Filing Date
JP19412481A Granted JPS5896876A (en) 1981-12-02 1981-12-02 Formation of wear and corrosion resistant film on metallic material

Country Status (1)

Country Link
JP (1) JPS5896876A (en)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS61106777A (en) * 1984-10-31 1986-05-24 Susumu Murao Corrosion resistant cast product
JPH03100184A (en) * 1989-09-13 1991-04-25 Nippon Sheet Glass Co Ltd Colored metal body
JPH0559572A (en) * 1991-09-02 1993-03-09 Kawasaki Steel Corp Aluminum alloy sheet excellent in press formability and corrosion resistance
JP2010215973A (en) * 2009-03-17 2010-09-30 Sumitomo Metal Ind Ltd Surface-treated galvanized metal material and surface treatment solution
JP2013084894A (en) * 2011-09-28 2013-05-09 Fujifilm Corp Substrate with insulating layer, semiconductor device using the same, photoelectric conversion element, light-emitting element, and electronic circuit
JP2015214131A (en) * 2014-05-09 2015-12-03 ホンタンサワット ワラポン Inorganic micro-film substrate and production method thereof

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS55167156A (en) * 1979-06-08 1980-12-26 Matsushita Electric Works Ltd Manufacture of product having siliceous film
JPS5625969A (en) * 1979-08-04 1981-03-12 Matsushita Electric Works Ltd Manufacture of product having glassy film

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS55167156A (en) * 1979-06-08 1980-12-26 Matsushita Electric Works Ltd Manufacture of product having siliceous film
JPS5625969A (en) * 1979-08-04 1981-03-12 Matsushita Electric Works Ltd Manufacture of product having glassy film

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS61106777A (en) * 1984-10-31 1986-05-24 Susumu Murao Corrosion resistant cast product
JPH03100184A (en) * 1989-09-13 1991-04-25 Nippon Sheet Glass Co Ltd Colored metal body
JPH0559572A (en) * 1991-09-02 1993-03-09 Kawasaki Steel Corp Aluminum alloy sheet excellent in press formability and corrosion resistance
JP2010215973A (en) * 2009-03-17 2010-09-30 Sumitomo Metal Ind Ltd Surface-treated galvanized metal material and surface treatment solution
JP2013084894A (en) * 2011-09-28 2013-05-09 Fujifilm Corp Substrate with insulating layer, semiconductor device using the same, photoelectric conversion element, light-emitting element, and electronic circuit
JP2015214131A (en) * 2014-05-09 2015-12-03 ホンタンサワット ワラポン Inorganic micro-film substrate and production method thereof

Also Published As

Publication number Publication date
JPS6214029B2 (en) 1987-03-31

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