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JPS6213387B2 - - Google Patents
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JPS6213387B2 - - Google Patents

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Publication number
JPS6213387B2
JPS6213387B2 JP8826978A JP8826978A JPS6213387B2 JP S6213387 B2 JPS6213387 B2 JP S6213387B2 JP 8826978 A JP8826978 A JP 8826978A JP 8826978 A JP8826978 A JP 8826978A JP S6213387 B2 JPS6213387 B2 JP S6213387B2
Authority
JP
Japan
Prior art keywords
condensed
zinc
coating
paint
aluminum
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
Application number
JP8826978A
Other languages
Japanese (ja)
Other versions
JPS5516020A (en
Inventor
Jiro Nakano
Takeshi Noguchi
Masao Nakita
Masanori Kinugasa
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.)
Tayca Corp
Original Assignee
Teikoku Kako 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 Teikoku Kako Co Ltd filed Critical Teikoku Kako Co Ltd
Priority to JP8826978A priority Critical patent/JPS5516020A/en
Publication of JPS5516020A publication Critical patent/JPS5516020A/en
Publication of JPS6213387B2 publication Critical patent/JPS6213387B2/ja
Granted legal-status Critical Current

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  • Paints Or Removers (AREA)

Description

【発明の詳細な説明】[Detailed description of the invention]

本発明は亜鉛板、亜鉛引き鉄板、あるいは亜鉛
系(被覆材を含む)の線材、棒材、管材、鋳造も
しくは鍛造品のような成型材のごとき被塗物に対
する塗膜の密着性の改良に関するものである。 塗料を亜鉛板、亜鉛引き鉄板等の被塗物に塗布
する場合、何の処理も施していない平滑な面に塗
布するとその密着性が頗る悪いので、サンドブラ
スト等をかけて凹凸を生じさせるか、あるいはリ
ン酸等で化成処理をした後に塗料を塗布すること
が通常行われている。しかしこれは余分な工程と
時間を必要とし、工費的ロスが大きい不利を有す
る。 本発明者等は塗料の組成を改良することによつ
て、塗料に化成処理と類似の作用を持たせること
ができるならば、化成処理を行つた後に塗料を塗
布するという通常行われている重複した工程が一
度の作業で行えることになり、作業工程の簡略
化、作業時間の短縮を通じ、コストの軽減が可能
になるとの構想に基づき鋭意研究を進めてきた結
果、塗料中に難溶性縮合リン酸アルミニウム塩と
即効性腐食性塩とを含有させておくと、亜鉛板、
亜鉛引き鉄板等に対する塗膜の密着性が改良され
るということを知見し本発明を完成したものであ
る。すなわち、本発明によるものは塗料中に縮合
リン酸アルミニウム塩および亜鉛に対する即効性
腐食性塩を併用することにある。 本発明によるものを更に具体的に説明すると、
本発明に用いられる縮合リン酸アルミニウム塩と
しては、ポリリン酸(トリポリリン酸等)および
メタリン酸(トリメタリン酸、テトラメタリン
酸、ヘキサメタリン酸等)のアルミニウム塩があ
る。 また、本発明に用いられる縮合リン酸アルミニ
ウム塩はJIS K―5101の方法での水溶分が0.01〜
5%の範囲に、好ましくは0.5〜2%の範囲にあ
ることが必要であり、上記の範囲より水溶分が少
ない場合には、塗膜の前記金属被塗物に対する密
着性向上は十分でないし、また上記範囲より水溶
分が多い場合には塗膜の密着性の向上は期待でき
ないし、塗膜性能も劣化する。オルトリン酸アル
ミニウム塩では上記密着性改良は十分でないの
に、上記特性を持つた縮合リン酸アルミニウム塩
が何故に塗膜の金属被塗物への密着性向上を得し
めるのかのメカニズムについては必ずしも明確な
解明をなし得ないが以下の如く考えられる。すな
わち、塗料中に存在する微量の水により縮合リン
酸イオンが一部遊離しており、この塗料を金属被
塗物に塗布すると、この一部遊離した縮合リン酸
イオンにより、上記塗布板の表面がリン酸塩処理
されることにより化成処理板と同じ効果が発現す
ることによる。更に、縮合リン酸イオンの塗布板
上でのリン酸塩処理的効果は塗布後、塗膜外から
の水分(例えば空気中の水分、雨水等)が塗膜中
に入つてくることにより、遊離してくる縮合リン
酸イオンによつても持続的に行われる。縮合リン
酸イオンはオルトリン酸イオンに比較して亜鉛に
対する反応性が大きいことが一般に認められてい
ることにより考えても、縮合リン酸アルミニウム
塩が効果的であることが首肯される。 また、水溶分が0.01〜5%の範囲であることが
要求されるのは、この程度の溶解度を持つものが
塗膜中に入れた場合、塗膜性能の低下をきたさ
ず、前記金属被塗物に対する縮合リン酸イオンの
反応性が最適であるからである。 上記のメカニズムは縮合リン酸塩(特にトリポ
リリン酸二水素アルミニウム)を無機ジンク塗料
に添加した場合、亜鉛末による白錆の発生をおさ
える効果があることよりもうなずける所である。 さらに、上記塗膜の密着性の改良には縮合リン
酸アルミニウム塩と共に亜鉛に対する即効性腐食
性塩を2%以下(塗膜中)併用すると上記の効果
がさらに改良されることがわかつた。すなわち、
この即効性腐食性塩としては、第一リン酸マンガ
ン、三塩基性硫酸鉛、シユウ酸第一錫、硫酸亜
鉛、珪弗化マグネシウム、珪弗化カルシウムを用
いることができる。 これらの即効性腐食性塩はその1種または2種
以上を混合して用いることは可能であるが、使用
量が2%をこえると塗膜性能の低下をきたし、特
に膨れが出易くなるので好ましくない。またこれ
らの腐食性塩は即効性であるので、前記金属被塗
物を短時間に侵し、縮合リン酸イオンと前記金属
イオンとの反応をしやすくし、金属被塗物上にリ
ン酸被膜の形成を容易にするというメカニズムに
より、亜鉛板、亜鉛引き鉄板等に対する塗膜の密
着性を改良する効果を促進する。これらの腐食性
塩の量または種類は縮合リン酸アルミニウム塩の
種類、ベヒクルの種類に応じて選択する必要があ
る。 実施例 塗料配合は次の第1表のようにした。
The present invention relates to improving the adhesion of a coating film to a coated object such as a zinc plate, a galvanized iron plate, or a zinc-based (including coating material) wire, bar, pipe, or molded material such as a cast or forged product. It is something. When applying paint to a surface to be coated, such as a zinc plate or galvanized iron plate, the adhesion will be extremely poor if applied to a smooth, untreated surface, so sandblasting or other methods may be used to create unevenness. Alternatively, coating is usually applied after chemical conversion treatment with phosphoric acid or the like. However, this requires extra steps and time, and has the disadvantage of a large loss in construction costs. The present inventors believe that if it is possible to give the paint a similar effect to that of chemical conversion treatment by improving the composition of the paint, then applying the paint after chemical conversion treatment is a common practice. As a result of intensive research based on the concept that this process can be performed in one operation, simplifying the work process and shortening the work time, it will be possible to reduce costs. When acid aluminum salt and fast-acting corrosive salt are contained, zinc plate,
The present invention was completed based on the finding that the adhesion of coating films to galvanized iron plates and the like is improved. That is, the present invention consists in the combined use of a condensed aluminum phosphate salt and a fast-acting corrosive salt for zinc in the paint. To explain the invention more specifically,
The condensed aluminum phosphate salts used in the present invention include aluminum salts of polyphosphoric acid (tripolyphosphoric acid, etc.) and metaphosphoric acid (trimetaphosphoric acid, tetrametaphosphoric acid, hexametaphosphoric acid, etc.). In addition, the condensed aluminum phosphate salt used in the present invention has a water soluble content of 0.01 to 0.01 by the method of JIS K-5101.
It is necessary that the water-soluble content is in the range of 5%, preferably in the range of 0.5 to 2%. If the water-soluble content is less than the above range, the adhesion of the coating film to the metal coating will not be improved sufficiently. Furthermore, if the water-soluble content is greater than the above range, no improvement in the adhesion of the coating film can be expected and the performance of the coating film will also deteriorate. The mechanism of why condensed aluminum phosphate salts with the above properties improve the adhesion of paint films to metal coatings is not clear, although aluminum orthophosphates do not sufficiently improve adhesion. Although no clear explanation can be given, it can be considered as follows. In other words, some condensed phosphate ions are liberated by the small amount of water present in the paint, and when this paint is applied to a metal object, the partially liberated condensed phosphate ions cause the surface of the coated plate to This is because the same effect as a chemically treated board is achieved by being treated with phosphate. Furthermore, the phosphate treatment effect of condensed phosphate ions on the coated plate is due to moisture from outside the coating film (e.g. moisture in the air, rainwater, etc.) entering the coating film, resulting in the release of condensed phosphate ions. It is also carried out continuously by condensed phosphate ions. Considering that it is generally accepted that condensed phosphate ions have greater reactivity toward zinc than orthophosphate ions, it is confirmed that condensed aluminum phosphate salts are effective. Furthermore, the reason why the water-soluble content is required to be in the range of 0.01 to 5% is that if a substance with this level of solubility is added to the coating film, it will not cause a decrease in coating performance, and the metal coating will not deteriorate. This is because the reactivity of condensed phosphate ions with respect to substances is optimal. The above mechanism is more understandable than the fact that when condensed phosphates (particularly aluminum dihydrogen tripolyphosphate) are added to inorganic zinc paints, they have the effect of suppressing the formation of white rust due to zinc dust. Furthermore, it has been found that the adhesion of the coating film can be further improved by using a condensed aluminum phosphate salt and a fast-acting corrosive salt against zinc in an amount of 2% or less (in the coating film). That is,
As the fast-acting corrosive salt, manganous monophosphate, tribasic lead sulfate, stannous oxalate, zinc sulfate, magnesium silicofluoride, and calcium silicofluoride can be used. It is possible to use one type or a mixture of two or more of these fast-acting corrosive salts, but if the amount used exceeds 2%, the performance of the coating will decrease, and blistering will especially occur. Undesirable. In addition, since these corrosive salts are fast-acting, they attack the metal coating in a short period of time, facilitating the reaction between condensed phosphate ions and the metal ions, and forming a phosphoric acid coating on the metal coating. The mechanism of facilitating formation promotes the effect of improving the adhesion of coating films to zinc plates, galvanized iron plates, etc. The amount or type of these corrosive salts must be selected depending on the type of condensed aluminum phosphate salt and the type of vehicle. Example The paint composition was as shown in Table 1 below.

【表】 なお、この塗料配合において具体的に用いられ
た各試料は以下のとおりである。 酸化チタン:帝国化工社製、商品名JR―602 ワニス固形分たる樹脂: 大日本インキ社製、商品名ベツコゾールJ524
(ヤシ油変性短油アルキツド樹脂、不揮発分60
%)と、大日本インキ社製、商品名スーパーベ
ツカミンJ―820(n―ブチルエーテル化メラ
ミン樹脂、不揮発分60%)とを固形分として前
者70%、後者30%の割合で混合したもの。 縮合リン酸塩: トリポリリン酸二水素アルミニウム(帝国化工
(株)製、Kボンド) 即効性腐食性塩: 即効性腐食性塩は以下の〜の試薬特級もの
を粉砕して使用した。 第一リン酸マンガン 三塩基性硫酸鉛 シユウ酸第一錫 硫酸亜鉛 珪弗化マグネシウム 珪弗化カルシウム 分散条件はペイントコンデイシヨナー(五十嵐
機械製)で30分間分散し、つぶは10μm以下
(JIS K5400A法)であつた。 然して上記のようにして得られた塗料は下記の
被塗板に対しバーコータ塗布し室温で1週間乾燥
して膜厚30〜34μmの塗層を形成した。 被塗板:亜鉛メツキ鋼板(JIS G3303) また、このようにして得られた塗装板に対し
て、下記する試験項目により試験し、その接着性
の評価をなした結果は後記する第2表の通りであ
る。 ごばん目テスト: 一次 室温1週間後 二次 40℃48時間没水、乾燥30分後
[Table] The samples specifically used in this paint formulation are as follows. Titanium oxide: manufactured by Teikoku Kako Co., Ltd., trade name JR-602 Varnish solid content resin: manufactured by Dainippon Ink Co., Ltd., trade name Betsukosol J524
(Coconut oil modified short oil alkyd resin, non-volatile content 60
%) and Dainippon Ink Co., Ltd., trade name Supervetsucomin J-820 (n-butyl etherified melamine resin, non-volatile content 60%), in a solid content of 70% of the former and 30% of the latter. Condensed phosphate: Aluminum dihydrogen tripolyphosphate (Teikoku Kako)
K-Bond Co., Ltd.) Instant-acting corrosive salt: As the instant-acting corrosive salt, the following special grade reagents were pulverized and used. Manganese monophosphate Tribasic lead sulfate Stannous oxalate Zinc sulfate Magnesium silicofluoride Calcium silicofluoride Dispersion conditions were as follows: Dispersion for 30 minutes using a paint conditioner (manufactured by Igarashi Kikai), with particles of 10 μm or less (JIS K5400A law). The paint obtained as described above was coated on the following coated plate using a bar coater and dried at room temperature for one week to form a coating layer with a thickness of 30 to 34 .mu.m. Coated plate: Galvanized steel plate (JIS G3303) The coated plate thus obtained was tested according to the test items listed below, and the results of the evaluation of adhesion are shown in Table 2 below. It is. First test: 1 week at room temperature, 2nd: 48 hours at 40°C, 30 minutes drying.

【表】 すなわち、第2表の結果によれば、本発明によ
る適量の腐食性塩添加によつて好ましい密着性向
上が得られることが明らかである。 以上説明したような本発明によるときは塗料中
に縮合リン酸アルミニウム塩および即効性腐食性
塩を含有させることにより亜鉛系金属被塗物に対
する塗膜の密着性を向上せしめ、特別な粗面化処
理を必要としないで時間的、工費的にロスの少な
い安定した塗膜を形成し得るものであり、しかも
ふくれやさびに対しても有効な防止を図ることが
できる等の作用効果を有しており、工業的にその
効果の大きい発明である。
[Table] That is, according to the results in Table 2, it is clear that a preferable improvement in adhesion can be obtained by adding an appropriate amount of corrosive salt according to the present invention. According to the present invention as explained above, by incorporating a condensed aluminum phosphate salt and a fast-acting corrosive salt into the paint, the adhesion of the paint film to the zinc-based metal coating is improved, and special surface roughening is achieved. It can form a stable coating film with little loss in terms of time and construction costs without requiring any treatment, and it also has the effect of effectively preventing blistering and rust. This invention has great industrial effects.

Claims (1)

【特許請求の範囲】 1 亜鉛系の金属被塗物に使用される塗料中に、
縮合リン酸アルミニウム塩と、塗膜ベースで2%
以下の第一リン酸マンガン、三塩基性硫酸鉛、シ
ユウ酸第一錫、硫酸亜鉛、ケイ弗化マグネシウ
ム、ケイ弗化カルシウムのいずれか1種または2
種以上を含有させてなる塗料組成物。 2 縮合リン酸塩としてトリポリリン酸二水素ア
ルミニウムまたはメタリン酸アルミニウムを用い
た特許請求の範囲第1項に記載の塗料組成物。
[Claims] 1. In the paint used for zinc-based metal coatings,
Condensed aluminum phosphate salt and 2% on coating base
Any one or two of the following manganese monophosphate, tribasic lead sulfate, stannous oxalate, zinc sulfate, magnesium silicofluoride, and calcium silicofluoride.
A coating composition containing at least one species. 2. The coating composition according to claim 1, which uses aluminum dihydrogen tripolyphosphate or aluminum metaphosphate as the condensed phosphate.
JP8826978A 1978-07-21 1978-07-21 Coating composition Granted JPS5516020A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP8826978A JPS5516020A (en) 1978-07-21 1978-07-21 Coating composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP8826978A JPS5516020A (en) 1978-07-21 1978-07-21 Coating composition

Publications (2)

Publication Number Publication Date
JPS5516020A JPS5516020A (en) 1980-02-04
JPS6213387B2 true JPS6213387B2 (en) 1987-03-26

Family

ID=13938165

Family Applications (1)

Application Number Title Priority Date Filing Date
JP8826978A Granted JPS5516020A (en) 1978-07-21 1978-07-21 Coating composition

Country Status (1)

Country Link
JP (1) JPS5516020A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS63121282U (en) * 1987-01-28 1988-08-05

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS55116768A (en) * 1979-03-02 1980-09-08 Teikoku Kako Kk Coating composition for protection of zinc from white rust
JPH0641570B2 (en) * 1984-10-08 1994-06-01 日本ペイント株式会社 Cationic electrodeposition coating composition
JP2590270B2 (en) * 1989-09-07 1997-03-12 アイシン化工 株式会社 Rust prevention paint composition

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS63121282U (en) * 1987-01-28 1988-08-05

Also Published As

Publication number Publication date
JPS5516020A (en) 1980-02-04

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