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JPS6354315B2 - - Google Patents

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Publication number
JPS6354315B2
JPS6354315B2 JP58173325A JP17332583A JPS6354315B2 JP S6354315 B2 JPS6354315 B2 JP S6354315B2 JP 58173325 A JP58173325 A JP 58173325A JP 17332583 A JP17332583 A JP 17332583A JP S6354315 B2 JPS6354315 B2 JP S6354315B2
Authority
JP
Japan
Prior art keywords
parts
lead
lead alloy
pigment
same
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
JP58173325A
Other languages
Japanese (ja)
Other versions
JPS6065075A (en
Inventor
Toshio Shinohara
Toshimiki Tsuji
Tooru Taki
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.)
Dai Nippon Toryo KK
Original Assignee
Dai Nippon Toryo 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 Dai Nippon Toryo KK filed Critical Dai Nippon Toryo KK
Priority to JP17332583A priority Critical patent/JPS6065075A/en
Publication of JPS6065075A publication Critical patent/JPS6065075A/en
Publication of JPS6354315B2 publication Critical patent/JPS6354315B2/ja
Granted legal-status Critical Current

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Description

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

本発明は防錆塗料組成物、詳しくは鱗片状鉛合
金顔料を含有する防錆塗料組成物に関する。 従来、鋼材等に対する防錆塗料組成物として
は、乾性油、アルキド樹脂、塩化ゴム、エポキシ
樹脂あるいはウレタン樹脂等の展色剤に、鉛系あ
るいはクロム酸塩系等の防錆顔料を混合してなる
防錆塗料が一般的に使用されていた。 前記防錆顔料としては、鉛粉、亜酸化鉛粉、鉛
丹、シアナミド鉛、鉛酸カルシウム等の鉛系ある
いは、ジンククロメート、ストロンチウムクロメ
ート、塩基性クロム酸鉛等のクロム酸塩系顔料が
広く使用されている。ところでこのような顔料は
防錆性が優れてはいるが、一般に粒状物であるた
め、塗膜中にこのような顔料が存在していても、
塗膜外部から侵入する水分や其の他腐食性物質の
遮断性はあまり期待出来なかつた。 一方、水分や腐食性物質の遮断性の優れた顔料
としては、鱗片状酸化鉄、アルミニウム粉末、マ
イカ、ガラスフレーク等が知られているが、これ
ら顔料は錆止め性が殆ど期待出来ない。 従つて、塗膜に遮断性と錆止め性を同時に付与
するためには夫々の機能を有する顔料を併用する
ことが考えられる。ところが、このように鱗片状
顔料と防錆顔料とを組合せて遮断性と錆止め性を
十分発揮させようとするのには、塗料中に両者を
かなり多量に混合する必要がある。この場合、顔
料容積濃度(PVC)が50%を越えるようになる
ため、塗膜の諸物性が低下するとともに、防錆性
も期待される程度には良い結果が得られない。 最近、遮断性と錆止め性を兼ね備えた顔料とし
て鱗片状鉛顔料が開発されているが、該顔料は柔
らかいため、塗料製造時における展色剤への顔料
分散工程において鱗片状顔料粒子の変形、折れ等
が生じ易いという欠点があつた。 近年、塗装工事費の高騰、大気中の腐食性物質
の増加等に伴つて、より長期間にわたつて優れた
防錆性を発揮する防錆塗料が要望されて来てい
る。 本発明は上記の如き実情に鑑みなされたもの
で、従来技術の各種問題点を解消し、腐食性物質
の遮断性と錆止め性に優れた塗膜を形成し得る防
錆塗料組成物を提供しようとするものである。 即ち、本発明は、 (1) 乾性油、アルキド樹脂、フエノール樹脂、塩
化ゴム樹脂及びビニル系樹脂から選ばれた少く
とも1種の展色剤100重量部に対して、 (2) 鱗片状鉛合金顔料10〜900重量部の割合から
なり、前記鱗片状鉛合金顔料が、Cu,Ni又は
Sbのいずれかの元素を0.05〜5重量%含有して
なる鉛合金からなる防錆塗料組成物に関する。 本発明に使用される展色剤としては、乾性油、
アルキド樹脂(フエノール変性、アクリル変性等
の変性アルキド樹脂を含む)、フエノール樹脂
(アルキド変性、乾性油変性等の変性フエノール
樹脂を含む)、塩化ゴム樹脂、ビニル系樹脂(ア
クリル樹脂を含む)から選ばれた少くとも1種の
乾性油又は合成樹脂である。これらの乾性油又は
合成樹脂は通常塗料用として市販されているもの
が全て支障なく使用可能である。 一方、本発明に使用される鱗片状鉛合金顔料
は、鉛にCu,Ni,Sb等のいずれかの元素を添加
して合金化した粒子をステアリン酸、ミネラルス
ピリツト等とともにボールミル等で鱗片状に加工
したもので、好ましくは粒子径10〜100μ、厚さ
0.5〜3μ程度のものである。 該鱗片状鉛合金顔料は、塗膜内で素材に対して
平行に幾層にも積層され、塗膜の強度を上げると
同時に、外部からの蒸気、水分、その他の腐食性
物質の透過、貫通を阻止するという効果と鉛顔料
のもつ優れた防錆性とを発揮するとともに、塗膜
に可撓性を付与出来る。 又、本発明の如く鉛合金化することにより、鉛
粒子に強度を付与出来、その結果塗料製造時にお
ける展色剤への顔料分散工程において、鱗片状顔
料粒子の変形、折れ等を防止できるのである。つ
まり、該顔料はほぼ完全な鱗片状の形態を保ちつ
つ塗料中に分散されるため、塗膜中で積層効果が
一段と向上し、その結果塗膜の防錆性も向上する
のである。 このような観点から、合金化成分の添加割合は
0.05重量%以上が好ましく、又鉛本来のもつ防錆
性を損わないためには5重量%以下程度が好まし
い。 本発明の組成物において、鱗片状鉛合金顔料は
展色剤100重量部に対して10〜900重量部の割合で
使用される。 前記範囲において、鱗片状鉛合金顔料が10重量
部に満たない場合は、水分等の腐食性物質の透過
阻視効果が低下し、従つて所期の防錆性が得られ
ず、逆に鱗片状鉛合金が900重量部を越えると、
塗膜の可撓性が低下し、もろくなるためいずれも
好ましくない。 本発明の組成物には必要に応じて、通常使用さ
れる着色顔料、体質顔料、その他防錆顔料、沈殿
防止剤、分散剤、希釈剤、可塑剤、ドライヤー、
ガラスフレーク等その他の鱗片状顔料、溶剤等を
添加、混合することが可能である。 かくして得られた本発明の塗料組成物は、ハ
ケ、ローラー、スプレー等通常の方法により被塗
物上に20μから200μになるよう塗布された後、常
温もしくは加熱により乾燥される。乾燥後得られ
た塗膜は、強度や耐食性、耐候性等に優れた性能
を有する。 また本発明の塗料組成物から得られた塗膜は特
に防錆性、塗膜物性に優れた性能を示すため、乾
燥後の塗膜上に塩化ゴム系塗料、アルキド樹脂系
塗料、エポキシ樹脂系塗料、ウレタン樹脂系塗
料、アクリル樹脂系塗料等の中塗り塗料や上塗り
塗料を塗布した塗装系は極めて優れた耐久性を示
す。加えて、本発明組成物から得られる塗膜はこ
れらの上塗り塗料に対しても優れた密着性を示
す。 以下、本発明の詳細を実施例及び比較例により
説明する。尚、「部」および「%」は「重量部」
および「重量%」をもつて示す。 実施例 1 アマニ油 45部 鱗片状鉛合金顔料A 25 酸化鉄 10 炭酸カルシウム 10 亜鉛華 4 沈降防止剤 1 乾燥剤 2 ミネラルターペン 100 前記鱗片状鉛合金Aは、Cuを0.1%含有する鉛
合金をアトマイズ法により微粒子化し、ステアリ
ン酸2%及びミネラルスピリツトを添加し、ポー
ルミルによつて鱗片状に加工した不揮発分88.7%
のペーストで、粒子径は10〜50μのものである。 実施例 2 大豆油変性中油型アルキド樹脂(油長50%、酸
価5) 30部 鱗片状鉛合金顔料B 20 酸化鉄 10 タルク 5 乾燥剤 3 皮張り防止剤 1 沈降防止剤 1 ミネラルスピリツト 30 100 前記鱗片状鉛合金顔料Bは、Niを0.1%含有す
る鉛合金を実施例1と同様の方法で加工した不揮
発分90.6%のペーストで、粒子径は10〜50μのも
のである。 実施例 3 大豆油変性中油型アルキド樹脂(実施例2と同
一) 15.0部 塩化ゴム(旭電化工業(株)製) 15.0 塩素化パラフイン40% 7.0 鱗片状鉛合金顔料C 20.0 酸化鉄 4.5 乾燥剤 2.0 皮張り防止剤 0.5 沈降防止剤 1.0 キシロール 35.0 100.0 前記鱗片状鉛合金顔料Cは、Sbを1%含有す
る鉛合金を実施例1と同様の方法で加工した、不
揮発分91.6%のペーストで、粒子径は10〜50μの
ものである。 実施例 4 塩化ゴム(実施例3と同一) 25部 塩素化パラフイン40% 10 鱗片状鉛合金顔料A 30 酸化鉄 4 沈降防止剤 1 キシロール 30 100 実施例 5 アクリル樹脂(大日本インキ化学工業(株)製、商
品名アクリデイツクA―169、不揮発分50%)
30部 鱗片状鉛合金顔料B 30 酸化鉄 4 沈降防止剤 1 キシロール 35 100 実施例 6 塩化ビニル樹脂(ユニオンカーバイド社製 商
品名:VYHH) 20部 ジブチルフタレート(DBP) 9 鱗片状鉛合金顔料C 10 酸化鉄 5 沈降防止剤 1 メチルイソブチルケトン 25 キシロール 20 酢酸ブチル 10 100 実施例 7 フエノール樹脂(日立化成工業(株)製商品名:ヒ
タノール1131) 20部 大豆油変性中油型アルキド樹脂(実施例2と同
一) 15 トルオール 16 酢酸エチル 15 鱗片状鉛合金顔料A 30 酸化鉄 100 比較例 1 アマニ油 45部 鉛粉(粒子径10〜50μの球状) 25 酸化鉄 10 炭酸カルシウム 10 沈降防止剤 1 亜鉛華 4 乾燥剤 2 ミネラルターペン 100 比較例 2 大豆油変性中油型アルキド樹脂(実施例2と同
一) 30部 鉛粉(比較例1と同一) 20 酸化鉄 5 マイカ 10 乾燥剤 5 皮張り防止剤 1 沈降防止剤 1 ミネラルスピリツト 28 100 比較例 3 大豆油変性中油型アルキド樹脂(実施例2と同
一) 25部 鉛粉(比較例1と同一) 30 酸化鉄 5 天然MIO(鱗片状酸化鉄) 10 乾燥剤 5 皮張り防止剤 1 沈降防止剤 1 ミネラルスピリツト 23 100 比較例 4 大豆油変性中油型アルキド樹脂(実施例2と同
一) 15.0部 塩化ゴム(実施例3と同一) 15.0 塩素化パラフイン40% 7.0 鉛粉(比較例1と同一) 15.0 酸化鉄 4.5 アルミ粉 10.0 乾燥剤 2.0 皮張り防止剤 0.5 沈降防止剤 1.0 キシロール 30.0 100.0 前記アルミ粉として、東洋アルミニウム(株)製商
品名アルペースト1100N(ペースト状:固型分64
%、ミネラルターペン分散)を使用した。 比較例 5 大豆油変性中油型アルキド樹脂(実施例2と同
一) 15.0部 塩化ゴム(実施例3と同一) 15.0 塩素化パラフイン40% 7.0 鉛粉(比較例1と同一) 20.0 酸化鉄 5.0 天然MIO 10.0 乾燥剤 2.0 皮張り防止剤 0.5 沈降防止剤 1.0 キシロール 24.5 100.0 比較例 6 塩化ゴム(実施例3と同一) 25部 塩素化パラフイン40% 10 鉛粉(比較例1と同一) 15 酸化鉄 5 マイカ 15 沈降防止剤 1 キシロール 29 100 比較例 7 塩化ゴム(実施例3と同一) 25部 塩素化パラフイン40% 10 鉛粉(比較例1と同一) 25 酸化鉄 5 アルミ粉(較例4と同一) 10 キシロール 25 100 比較例 8 アクリル樹脂(実施例5と同一) 30部 鉛粉(比較例1と同一) 15 酸化鉄 5 ガラスフレーク 10 沈降防止剤 1 キシロール 39 100 前記ガラスフレークとして、日本ガラス繊維(株)
製商品名CF―150(粒子径0.03〜6mm)を使用し
た。 比較例 9 アクリル樹脂(実施例5と同一) 30部 天然MIO 10 鉛粉(比較例1と同一) 20 酸化鉄 5 沈降防止剤 1 キシロール 34 100 比較例 10 塩化ビニル樹脂(実施例6と同一) 20部 ジブチルフタレート(DBP) 9 鉛粉(比較例1と同一) 10 酸化鉄 5 マイカ 10 沈降防止剤 1 メチルイソブチルケトン 20 キシロール 15 酢酸ブチル 10 100 比較例 11 塩化ビニル樹脂(実施例6と同一) 20部 DBP 9 天然MIO 10 鉛粉(比較例1と同一) 20 酸化鉄 5 沈降防止剤 1 メチルイソブチルケトン 15 キシロール 10 酢酸ブチル 10 100 前記各実施例および比較例で示した塗料組成物
は、沈降防止剤、体質顔料および着色顔料を予め
展色剤に常法により分散せしめ、ついで鱗片状鉛
合金顔料又は鉛粉を加えデイスパーにて撹拌し製
造した。 得られた各塗料組成物は、サンドペーパーで研
磨後トリクレンで脱脂した磨軟鋼板上に乾燥膜厚
70μ(35μ×2回)になるよう塗装し、乾燥後比較
試験に供した。試験結果を表―1および表―2に
示す。
The present invention relates to a rust-preventing paint composition, and more particularly to a rust-preventing paint composition containing a scaly lead alloy pigment. Conventionally, rust-preventing paint compositions for steel materials have been prepared by mixing a color vehicle such as drying oil, alkyd resin, chlorinated rubber, epoxy resin, or urethane resin with a lead-based or chromate-based rust preventive pigment. Anti-rust paints were commonly used. The anti-corrosion pigments include lead-based pigments such as lead powder, zinc oxide powder, red lead, lead cyanamide, and calcium leadate, and chromate-based pigments such as zinc chromate, strontium chromate, and basic lead chromate. It is used. By the way, although such pigments have excellent rust prevention properties, they are generally granular, so even if such pigments are present in the paint film,
The ability to block moisture and other corrosive substances from entering from outside the coating film was not very promising. On the other hand, scaly iron oxide, aluminum powder, mica, glass flakes, and the like are known as pigments that have excellent barrier properties against moisture and corrosive substances, but these pigments are hardly expected to have antirust properties. Therefore, in order to impart barrier properties and rust-preventing properties to the coating film at the same time, it is conceivable to use pigments having the respective functions in combination. However, in order to achieve sufficient barrier and rust preventive properties by combining a scale pigment and a rust preventive pigment in this way, it is necessary to mix a fairly large amount of both in the paint. In this case, since the pigment volume concentration (PVC) exceeds 50%, the various physical properties of the coating film deteriorate, and the desired rust prevention properties are not obtained. Recently, scaly lead pigments have been developed as pigments that have both barrier properties and rust-inhibiting properties.However, because these pigments are soft, the scaly pigment particles may be deformed or broken during the pigment dispersion process in the vehicle during paint manufacturing. The disadvantage was that it was easy for problems such as the following to occur. In recent years, with the rise in painting costs and the increase in corrosive substances in the atmosphere, there has been a demand for rust-preventing paints that exhibit excellent rust-prevention properties over a longer period of time. The present invention has been made in view of the above-mentioned circumstances, and it is an object of the present invention to provide a rust-preventing paint composition capable of solving the various problems of the prior art and forming a coating film with excellent barrier properties against corrosive substances and rust-preventing properties. That is. That is, the present invention provides: (1) 100 parts by weight of at least one color vehicle selected from drying oils, alkyd resins, phenolic resins, chlorinated rubber resins, and vinyl resins, (2) lead flakes; It consists of an alloy pigment in a proportion of 10 to 900 parts by weight, and the flaky lead alloy pigment
The present invention relates to a rust-preventing paint composition made of a lead alloy containing 0.05 to 5% by weight of any one of the elements Sb. Color vehicles used in the present invention include drying oils,
Select from alkyd resins (including modified alkyd resins such as phenol modified and acrylic modified), phenolic resins (including modified phenolic resins such as alkyd modified and drying oil modified), chlorinated rubber resins, and vinyl resins (including acrylic resins). at least one drying oil or synthetic resin. As these drying oils or synthetic resins, all those commercially available for use in paints can be used without any problem. On the other hand, the flaky lead alloy pigment used in the present invention is made by adding alloyed particles of lead with one of the elements such as Cu, Ni, Sb, etc. together with stearic acid, mineral spirits, etc. in a ball mill etc. to form flaky lead alloy pigments. Preferably, the particle size is 10 to 100μ and the thickness is
It is about 0.5 to 3μ. The scaly lead alloy pigment is layered in parallel to the material within the paint film, increasing the strength of the paint film and at the same time preventing the permeation and penetration of external steam, moisture, and other corrosive substances. It has the effect of inhibiting corrosion and exhibits the excellent rust prevention properties of lead pigments, and can also impart flexibility to the coating film. Furthermore, by alloying lead as in the present invention, it is possible to impart strength to the lead particles, and as a result, it is possible to prevent deformation, breakage, etc. of the scale-like pigment particles during the pigment dispersion process in the color vehicle during paint production. be. In other words, since the pigment is dispersed in the paint while maintaining an almost perfect scale-like form, the lamination effect in the paint film is further improved, and as a result, the rust prevention properties of the paint film are also improved. From this point of view, the addition ratio of alloying components is
It is preferably 0.05% by weight or more, and preferably about 5% by weight or less in order not to impair the rust prevention properties inherent to lead. In the composition of the present invention, the flaky lead alloy pigment is used in an amount of 10 to 900 parts by weight per 100 parts by weight of the vehicle. In the above range, if the amount of the scaly lead alloy pigment is less than 10 parts by weight, the effect of blocking the penetration of corrosive substances such as moisture will be reduced, and the desired rust prevention property will not be obtained, and on the contrary, the scaly lead alloy pigment will be less than 10 parts by weight. If the lead alloy exceeds 900 parts by weight,
Both are unfavorable because the coating film becomes less flexible and brittle. The composition of the present invention may contain commonly used coloring pigments, extender pigments, other rust preventive pigments, suspending agents, dispersants, diluents, plasticizers, dryers,
It is possible to add and mix other scaly pigments such as glass flakes, solvents, etc. The thus obtained coating composition of the present invention is applied onto an object to be coated to a thickness of 20 to 200 μ by a conventional method such as brushing, roller, or spraying, and then dried at room temperature or by heating. The coating film obtained after drying has excellent properties such as strength, corrosion resistance, and weather resistance. In addition, since the coating film obtained from the coating composition of the present invention exhibits particularly excellent rust prevention properties and physical properties of the coating film, it is possible to apply chlorinated rubber coatings, alkyd resin coatings, epoxy resin coatings, etc. on the coating film after drying. Paints, urethane resin paints, acrylic resin paints, and other intermediate and top coat coating systems exhibit extremely high durability. In addition, the coating film obtained from the composition of the present invention exhibits excellent adhesion to these top coats. The details of the present invention will be explained below with reference to Examples and Comparative Examples. In addition, "parts" and "%" are "parts by weight"
and "% by weight". Example 1 Linseed oil 45 parts Flaky lead alloy pigment A 25 Iron oxide 10 Calcium carbonate 10 Zinc white 4 Anti-settling agent 1 Desiccant 2 Mineral turpentine 3 100 The flaky lead alloy A is a lead alloy containing 0.1% Cu. 88.7% non-volatile content made by atomizing into fine particles, adding 2% stearic acid and mineral spirits, and processing into scales using a pole mill.
The paste has a particle size of 10 to 50μ. Example 2 Soybean oil modified medium oil type alkyd resin (oil length 50%, acid value 5) 30 parts scaly lead alloy pigment B 20 iron oxide 10 talc 5 desiccant 3 anti-skinning agent 1 anti-settling agent 1 mineral spirit 30 100 The flaky lead alloy pigment B is a paste with a non-volatile content of 90.6% produced by processing a lead alloy containing 0.1% Ni in the same manner as in Example 1, and has a particle size of 10 to 50μ. Example 3 Soybean oil-modified medium oil type alkyd resin (same as Example 2) 15.0 parts Chlorinated rubber (manufactured by Asahi Denka Kogyo Co., Ltd.) 15.0 Chlorinated paraffin 40% 7.0 Scaly lead alloy pigment C 20.0 Iron oxide 4.5 Desiccant 2.0 Anti-skinning agent 0.5 Anti-settling agent 1.0 Xylol 35.0 100.0 The flaky lead alloy pigment C is a paste with a non-volatile content of 91.6% produced by processing a lead alloy containing 1% Sb in the same manner as in Example 1. The diameter is 10-50μ. Example 4 Chlorinated rubber (same as Example 3) 25 parts Chlorinated paraffin 40% 10 Scaly lead alloy pigment A 30 Iron oxide 4 Anti-settling agent 1 Xylol 30 100 Example 5 Acrylic resin (Dainippon Ink & Chemicals Co., Ltd.) ), product name Acrydik A-169, non-volatile content 50%)
30 parts scaly lead alloy pigment B 30 iron oxide 4 anti-settling agent 1 xylol 35 100 Example 6 Vinyl chloride resin (manufactured by Union Carbide, trade name: VYHH) 20 parts dibutyl phthalate (DBP) 9 scaly lead alloy pigment C 10 Iron oxide 5 Anti-settling agent 1 Methyl isobutyl ketone 25 Xylol 20 Butyl acetate 10 100 Example 7 Phenol resin (trade name: Hytanol 1131, manufactured by Hitachi Chemical Co., Ltd.) 20 parts Soybean oil modified medium oil alkyd resin (Example 2 and Same) 15 Toluene 16 Ethyl acetate 15 Scaly lead alloy pigment A 30 Iron oxide 4 100 Comparative example 1 Linseed oil 45 parts Lead powder (spherical with particle size 10-50μ) 25 Iron oxide 10 Calcium carbonate 10 Anti-settling agent 1 Zinc white 4 Desiccant 2 Mineral turpentine 3 100 Comparative example 2 Soybean oil modified medium oil type alkyd resin (same as Example 2) 30 parts lead powder (same as Comparative example 1) 20 Iron oxide 5 Mica 10 Desiccant 5 Anti-skinning agent 1 Anti-settling agent 1 Mineral spirits 28 100 Comparative example 3 Soybean oil modified medium oil alkyd resin (same as Example 2) 25 parts lead powder (same as Comparative example 1) 30 Iron oxide 5 Natural MIO (scaly iron oxide) 10 Desiccant 5 Anti-skinning agent 1 Anti-settling agent 1 Mineral spirits 23 100 Comparative example 4 Soybean oil modified medium oil type alkyd resin (same as Example 2) 15.0 parts Chlorinated rubber (same as Example 3) 15.0 Chlorinated paraffin 40 % 7.0 Lead powder (same as Comparative Example 1) 15.0 Iron oxide 4.5 Aluminum powder 10.0 Desiccant 2.0 Anti-skinning agent 0.5 Anti-settling agent 1.0 Xylol 30.0 100.0 As the aluminum powder, Alpaste 1100N (trade name, manufactured by Toyo Aluminum Co., Ltd.) Paste: solid content 64
%, mineral turpentine dispersion) was used. Comparative Example 5 Soybean oil modified medium oil alkyd resin (same as Example 2) 15.0 parts Chlorinated rubber (same as Example 3) 15.0 Chlorinated paraffin 40% 7.0 Lead powder (same as Comparative Example 1) 20.0 Iron oxide 5.0 Natural MIO 10.0 Desiccant 2.0 Anti-skinning agent 0.5 Anti-settling agent 1.0 Xylol 24.5 100.0 Comparative example 6 Chlorinated rubber (same as Example 3) 25 parts chlorinated paraffin 40% 10 Lead powder (same as Comparative example 1) 15 Iron oxide 5 Mica 15 Anti-settling agent 1 Xylol 29 100 Comparative example 7 Chlorinated rubber (same as Example 3) 25 parts chlorinated paraffin 40% 10 Lead powder (same as Comparative example 1) 25 Iron oxide 5 Aluminum powder (same as Comparative example 4) 10 Xylol 25 100 Comparative Example 8 Acrylic resin (same as Example 5) 30 parts lead powder (same as Comparative Example 1) 15 Iron oxide 5 Glass flakes 10 Anti-settling agent 1 Xylol 39 100 As the glass flakes, Nippon Glass Fiber ( KK)
Product name CF-150 (particle size 0.03 to 6 mm) was used. Comparative Example 9 Acrylic resin (same as Example 5) 30 parts natural MIO 10 Lead powder (same as Comparative Example 1) 20 Iron oxide 5 Anti-settling agent 1 Xylol 34 100 Comparative Example 10 Vinyl chloride resin (same as Example 6) 20 parts dibutyl phthalate (DBP) 9 Lead powder (same as Comparative Example 1) 10 Iron oxide 5 Mica 10 Anti-settling agent 1 Methyl isobutyl ketone 20 Xylol 15 Butyl acetate 10 100 Comparative example 11 Vinyl chloride resin (same as Example 6) 20 parts DBP 9 Natural MIO 10 Lead powder (same as Comparative Example 1) 20 Iron oxide 5 Anti-settling agent 1 Methyl isobutyl ketone 15 Xylol 10 Butyl acetate 10 100 The coating compositions shown in the above examples and comparative examples are The inhibitor, extender pigment, and coloring pigment were previously dispersed in a color vehicle by a conventional method, and then the scaly lead alloy pigment or lead powder was added and stirred with a disper to produce the product. Each of the obtained paint compositions was coated on a polished mild steel plate that had been polished with sandpaper and degreased with trichloride to give a dry film thickness.
It was coated to a thickness of 70μ (35μ x 2 times), and after drying it was subjected to a comparative test. The test results are shown in Table-1 and Table-2.

【表】【table】

【表】【table】

【表】【table】

【表】【table】

【表】 前記比較試験結果表―1及び表―2より明らか
に本発明の塗料組成物から得られた塗膜は、従来
公知の塗料組成物あるいは比較例塗料組成物から
得られた塗膜に比して耐食性が一段と向上すると
ともに塗膜物性も優れたものであつた。
[Table] From the comparative test results Table 1 and Table 2, it is clear that the coating film obtained from the coating composition of the present invention is superior to the coating film obtained from the conventionally known coating composition or the comparative coating composition. In comparison, the corrosion resistance was further improved and the physical properties of the coating film were also excellent.

Claims (1)

【特許請求の範囲】 1 乾性油、アルキド樹脂、フエノール樹脂、塩
化ゴム樹脂及びビニル系樹脂から選ばれた少くと
も1種の展色剤100重量部に対して、 2 鱗片状鉛合金顔料10〜900重量部の割合から
なり、前記鱗片状鉛合金顔料が、Cu,Ni又はSb
のいずれかの元素を0.05〜5重量%含有してなる
鉛合金からなる防錆塗料組成物。
[Scope of Claims] 1. For 100 parts by weight of at least one color vehicle selected from drying oil, alkyd resin, phenolic resin, chlorinated rubber resin, and vinyl resin, 2. 10 to 10 parts of scaly lead alloy pigment. 900 parts by weight, and the flaky lead alloy pigment contains Cu, Ni or Sb.
An anticorrosive paint composition made of a lead alloy containing 0.05 to 5% by weight of any of the following elements.
JP17332583A 1983-09-20 1983-09-20 Rust-inhibiting paint composition Granted JPS6065075A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP17332583A JPS6065075A (en) 1983-09-20 1983-09-20 Rust-inhibiting paint composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP17332583A JPS6065075A (en) 1983-09-20 1983-09-20 Rust-inhibiting paint composition

Publications (2)

Publication Number Publication Date
JPS6065075A JPS6065075A (en) 1985-04-13
JPS6354315B2 true JPS6354315B2 (en) 1988-10-27

Family

ID=15958336

Family Applications (1)

Application Number Title Priority Date Filing Date
JP17332583A Granted JPS6065075A (en) 1983-09-20 1983-09-20 Rust-inhibiting paint composition

Country Status (1)

Country Link
JP (1) JPS6065075A (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5326394A (en) * 1989-06-15 1994-07-05 Cobb James C Oil based paint
TW200617120A (en) * 2004-05-31 2006-06-01 Nippon Steel Corp Paint for steel material having corrosion resistance and rust resistance

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5193934A (en) * 1975-02-15 1976-08-18 BOSEITORY OSOSEI BUTSU

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5193934A (en) * 1975-02-15 1976-08-18 BOSEITORY OSOSEI BUTSU

Also Published As

Publication number Publication date
JPS6065075A (en) 1985-04-13

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