JPS60133072A - Primary rust preventing coating material composition having good weldability - Google Patents

Primary rust preventing coating material composition having good weldability

Info

Publication number
JPS60133072A
JPS60133072A JP24088683A JP24088683A JPS60133072A JP S60133072 A JPS60133072 A JP S60133072A JP 24088683 A JP24088683 A JP 24088683A JP 24088683 A JP24088683 A JP 24088683A JP S60133072 A JPS60133072 A JP S60133072A
Authority
JP
Japan
Prior art keywords
welding
zinc
weight
zinc flakes
good weldability
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.)
Pending
Application number
JP24088683A
Other languages
Japanese (ja)
Inventor
Koichi Saneto
実藤 公一
Kenichi Hirabayashi
健一 平林
Shiro Shimatani
嶋谷 四郎
Shunji Isoda
磯田 俊司
Hajime Okamoto
一 岡本
Osamu Kawada
修 川田
Shinichi Ishihara
石原 慎一
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.)
Mitsui Mining and Smelting Co Ltd
Mitsui Engineering and Shipbuilding Co Ltd
Nippon Paint Co Ltd
Mitsui Zosen KK
Original Assignee
Mitsui Mining and Smelting Co Ltd
Mitsui Engineering and Shipbuilding Co Ltd
Nippon Paint Co Ltd
Mitsui Zosen 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 Mitsui Mining and Smelting Co Ltd, Mitsui Engineering and Shipbuilding Co Ltd, Nippon Paint Co Ltd, Mitsui Zosen KK filed Critical Mitsui Mining and Smelting Co Ltd
Priority to JP24088683A priority Critical patent/JPS60133072A/en
Publication of JPS60133072A publication Critical patent/JPS60133072A/en
Pending legal-status Critical Current

Links

Abstract

PURPOSE:The titled composition, containing a vehicle and zinc flakes in a specific proportion, capable of giving improved weldability to a steel plate by applying to the steel plate before the working and welding, particularly gas shielding welding, and useful for large-sized steel structures, e.g. ships and plants. CONSTITUTION:A composition obtained by incorporating (A) 5-10wt%, based on the dry weight, vehicle, e.g. a partial hydrolyzate condensate to an alkyl silicate of the formula Si(OR)4 (R is ethyl, butyl or cellosolve, etc.) with (B) 15-60wt% zinc flakes, preferably containing 3wt% organic pulverizing agent, and having <=100mu maximum length, 1.5-30mu average major axis, <=5mu average thickness and >=3 aspect ratio.

Description

【発明の詳細な説明】 本発明は塗料組成物に関し、さらに詳しくは、加工前の
鋼板に塗装して、溶接時、特にガスシールド溶接時に良
好な溶接性を与える一次防錆塗料組成物に関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a coating composition, and more particularly to a primary anticorrosive coating composition that is applied to a steel plate before processing and provides good weldability during welding, particularly gas shield welding.

従来、船舶、橋梁、タンク、プラント等の大型鉄鋼構造
物を建造する場合、建造中の発錆を防止し、防錆塗装を
完全なものとするため、また経済的および能率的に建造
するため、加工前の原材料をプラスチングまたは酸洗い
してミルスケールや錆を除去したのち、−次防錆塗料を
塗装することが一般的に行がわれでいる。
Conventionally, when constructing large steel structures such as ships, bridges, tanks, and plants, it has been necessary to prevent rust during construction, to ensure complete anti-rust coating, and to construct economically and efficiently. It is common practice to remove mill scale and rust by plasting or pickling raw materials before processing, and then apply a second anti-corrosion paint.

従来、用いられている一次防錆塗料としては、ポリビニ
ルブチラール樹脂−リン酸系のウォッシープライマ−、
エポキシ樹脂等の有機樹脂−高濃度亜鉛末系の有機ジン
クリッチ被インド、無機バインダー−高濃度亜鉛末系の
無機ジンクリッチペイント等がある。しかしながら、ポ
リビニルブチラール樹脂、エポキシ樹脂等の有機樹脂は
高温分解または燃焼を起こし、また高濃度亜鉛末系のジ
ンクリッチペイントでは亜鉛末の沸点が低いために気化
し、そのため溶接時に気体を発生してブローホールを発
生しやすいという欠点がある。特に炭酸ガス溶接法のよ
うなガスシールド溶接法においては、被覆アーク溶接法
やサブマーソrアーク溶接法に比べて浴融金属の冷却速
度が速いため、従来の一次防錆塗料を塗装した鋼板では
ブローホールが多量に発生するという欠点があった。近
年、造船工業界では炭酸ガス溶接法の使用が多くなる傾
向にあり、炭酸ガス溶接等のガスシールド溶接時に良好
な溶接性を与える一次防錆塗料組成物の開発が望まれて
いた。
Conventionally used primary rust-preventing paints include polyvinyl butyral resin-phosphoric acid-based washy primer,
There are organic zinc rich paints based on organic resin such as epoxy resin and high concentration zinc dust, and inorganic zinc rich paints based on inorganic binder and high concentration zinc dust. However, organic resins such as polyvinyl butyral resin and epoxy resin decompose or burn at high temperatures, and zinc-rich paints based on high-concentration zinc dust vaporize due to the low boiling point of zinc dust, which generates gas during welding. It has the disadvantage of being prone to blowholes. In particular, in gas shield welding methods such as carbon dioxide welding, the cooling rate of the bath molten metal is faster than in coated arc welding or submersor arc welding. The drawback was that a large number of holes were generated. In recent years, the use of carbon dioxide gas welding has been increasing in the shipbuilding industry, and there has been a desire to develop a primary rust-preventing paint composition that provides good weldability during gas shield welding such as carbon dioxide gas welding.

一方、溶融金属を固化すると、金属内部に多数の気孔が
発生するが、脱酸剤を添加すると気孔が減少することは
よく知られている。このため、−次防錆塗料に脱酸性顔
料を添加して被覆アーク溶接法やサブマージドアーク溶
接法の溶接性を改良する試みがなされているが(特8昭
47−22923号)、これを炭酸ガス溶接法に適用し
ても必ずしも良好な溶接性が得られなかった〇 本発明の目的は、従来の一次防錆塗料組成物の有する欠
点をなくシ、特にガスシールド溶接時に良好な溶接性を
与える一次防錆塗料組成物を提供することにある。
On the other hand, when molten metal is solidified, a large number of pores are generated inside the metal, and it is well known that adding a deoxidizing agent reduces the number of pores. For this reason, attempts have been made to improve the weldability of coated arc welding and submerged arc welding by adding deoxidizing pigments to secondary anti-corrosion paints (Special Patent No. 8, 1972-22923); Even when applied to carbon dioxide gas welding, good weldability was not necessarily obtained.The purpose of the present invention is to eliminate the drawbacks of conventional primary rust preventive paint compositions, and to improve weldability, especially during gas shield welding. The object of the present invention is to provide a primary anticorrosive paint composition that provides the following properties.

本発明者らはこの目的達成のため鋭意研究の結果、炭酸
ガス溶接時のブローホール発生を減少させるには、−次
防錆塗料組成物に用いる亜鉛の使用量を低減させ、かつ
用いる亜鉛棟としてはフレーク状亜鉛を用いることが不
可欠であることを見い出して本発明に到達した。
As a result of intensive research to achieve this objective, the present inventors have found that, in order to reduce the occurrence of blowholes during carbon dioxide gas welding, - The present invention was achieved by discovering that it is essential to use flaky zinc.

本発明は、乾量基準で展色剤5〜20重菫饅、亜鉛フレ
ーク15〜60重Ji%含むことを特徴とする。
The present invention is characterized in that it contains 5 to 20 weight percent of a color vehicle and 15 to 60 weight percent of zinc flakes on a dry basis.

本発明に用いられる展色剤としては、高温灼熱減量の少
ないものを用いることが望ましく、かつその使用量も少
ない程良好な溶接性を示す。
As the color vehicle used in the present invention, it is desirable to use one that exhibits less loss on high-temperature ignition, and the smaller the amount used, the better the weldability will be.

このような展色剤としては、例えばアルギルシリケ−)
 5l(OR)4(式中Rはエチル基、ブチル基、セロ
ソルブ等を意味する)の部分加水分解縮合物及び所望に
よりさらにアルコール可溶性有機樹脂(例工id’ y
Je +Jビニルブチラール、?リビニルアルコール、
ポリアクリル酸エステル等)を、5io2/有機樹脂固
形分が重量比で10010〜60/40の範囲となるよ
うにブレンドして用いる。
As such a color vehicle, for example, argyl silica)
5l(OR)4 (in the formula, R means an ethyl group, a butyl group, a cellosolve, etc.) and, if desired, an alcohol-soluble organic resin (eg
Je +J vinyl butyral,? libinyl alcohol,
Polyacrylic acid ester, etc.) are blended and used so that the weight ratio of 5io2/organic resin solids is in the range of 10010 to 60/40.

また有機樹脂系展色剤として、例えばエポキシ樹脂、ウ
レタン樹脂叫を使用することもできる。
Further, as the organic resin color vehicle, for example, epoxy resin or urethane resin can also be used.

本発明の組成物中の展色剤の使用蓋は乾燥塗膜中5〜2
0重量%の範囲であシ、20重量%を超えると炭酸ガス
溶接時のブローホール発生が多くなシ、また5重量多未
満では塗膜結合力が弱く、実質的に塗膜形成が難かしく
なる。
The use of the color vehicle in the composition of the present invention is 5 to 2 times in the dry coating.
If it is in the range of 0% by weight, it is fine, if it exceeds 20% by weight, blowholes will occur frequently during carbon dioxide gas welding, and if it is less than 5% by weight, the bonding strength of the coating will be weak and it will be practically difficult to form a coating. Become.

本発明に用いる亜鉛は防錆顔料として不可欠で、乾量基
準で15〜60重量%用いるが、望ましくは20〜40
重量係である。ここで用いる亜鉛は、最大長さ100μ
以下、平均長径1.5〜3(Jtt、平均厚み5μ以下
、アス被りト比(長径/厚み)3以上のフレーク状亜鉛
を用いる必要がある。これは、スプレー時のスプレーガ
ンの詰シを防ぎ、充分な表面積を得るためである。かか
る亜鉛フレークは、球状亜鉛末に較べ比表面積(粉末単
位重量当シの表面8t )が犬きく粒子間の接触が密に
保たれる。ため防錆性に優れており、亜鉛使用量の大幅
な低減が可能である。又、その形状から溶接時の入熱に
よる燃焼が球状亜鉛末に較べ短時間に行なわれるため、
塗料組成物中の亜鉛は浴接ビードの冷却以前に完全燃焼
し、亜鉛の気化蒸気は系外に散逸しブローホールが避け
られる。また亜鉛フレークの製造時に有機系粉砕剤(ス
テアリン酸、オレイン酸などの高級脂肪酸又はそれらの
金属塩)が使用されるが、亜鉛フレーク中の有機粉砕剤
の含有量が多いと防錆性を低下させ、溶接時の熱による
CO2H2等に起因するブローホールの発生が多くなる
傾向にある。従って、亜鉛フレーク中の有機物の含有量
は3重蓋チ以下である事が望ましい。亜鉛フレークの使
用量は乾量基準で15〜60重量%用いる。60重N%
を超えると亜鉛の気化によるブローホールが多くなシ、
15重!−%以下の場合は防錆性が劣るからである。
Zinc used in the present invention is essential as a rust preventive pigment, and is used in an amount of 15 to 60% by weight on a dry weight basis, preferably 20 to 40% by weight.
He is in charge of weight. The zinc used here has a maximum length of 100μ
Below, it is necessary to use zinc flakes with an average major axis of 1.5 to 3 (Jtt), an average thickness of 5 μ or less, and an asperity coverage ratio (major axis/thickness) of 3 or more. This is to prevent corrosion and obtain a sufficient surface area.Such zinc flakes have a larger specific surface area (surface area of 8 tons per unit weight of powder) than spherical zinc powder, and close contact between particles can be maintained. It has excellent properties, making it possible to significantly reduce the amount of zinc used.Also, due to its shape, combustion due to heat input during welding takes place in a shorter time than with spherical zinc powder.
The zinc in the coating composition is completely combusted before the bath bead is cooled, and the vaporized zinc is dissipated outside the system, thereby avoiding blowholes. In addition, organic grinding agents (higher fatty acids such as stearic acid and oleic acid, or their metal salts) are used during the production of zinc flakes, but if the content of organic grinding agents in zinc flakes is high, the rust prevention properties will decrease. This tends to increase the occurrence of blowholes caused by CO2H2 and the like due to heat during welding. Therefore, it is desirable that the content of organic matter in the zinc flakes be 3 times or less. The amount of zinc flakes used is 15 to 60% by weight on a dry weight basis. 60 weight N%
If the
15 layers! -% or less, the rust prevention properties are poor.

本発明において、必須成分としての展色剤、亜鉛フレー
ク以外に必要に応じて通常用いられている溶剤、体質顔
料、着色顔料、一般防錆顔料、各種添加剤等を添加する
ことができる。
In the present invention, in addition to the color vehicle and zinc flakes as essential components, commonly used solvents, extender pigments, coloring pigments, general antirust pigments, various additives, etc. can be added as necessary.

本発明の塗料組成物は、プラスチングまたは酸洗い等に
よりミルスケールおよび錆を除去した部分に塗布すると
、長時間にわたシ鋼板の発錆を防止することができる。
When the coating composition of the present invention is applied to areas from which mill scale and rust have been removed by plasting, pickling, etc., it is possible to prevent rust from forming on steel plates for a long period of time.

′!l:た従来の一次防錆塗装組成物のように炭酸ガス
溶接においてブローホールを多発することなく、高能率
で溶接作業を行なうことができる。
′! 1: Unlike conventional primary anti-rust coating compositions, welding work can be performed with high efficiency without causing many blowholes during carbon dioxide gas welding.

以下、本発明組成物の製造例、実施例および比較例を述
べる。なお、下記例中の部および俤は重量部および重蓋
チを意味する。
Hereinafter, production examples, examples, and comparative examples of the composition of the present invention will be described. In addition, parts and 忤 in the following examples mean parts by weight and weight.

製造例1(展色剤の製造) エテルシリケート(日本コルコート化学(株)製、商品
名[エテルシリケート40J)38部およびイソプロピ
ルアルコール57部を攪拌機付容器に入れ、充分混合し
、40℃に保温しながら攪拌し、これにQ、IN塩酸0
.5部および水4.5部の混合物を1時間かけて滴下し
た。滴下終了後、40℃で5時間攪拌を続け、5lO2
分約15チのエチルシリケート部分加水分解縮合液を得
た。
Production Example 1 (Production of a color vehicle) 38 parts of ethersilicate (manufactured by Nippon Colcoat Chemical Co., Ltd., trade name [Ethersilicate 40J) and 57 parts of isopropyl alcohol were placed in a container equipped with a stirrer, mixed thoroughly, and kept at 40°C. While stirring, add Q, IN hydrochloric acid 0
.. A mixture of 5 parts and 4.5 parts of water was added dropwise over 1 hour. After dropping, continue stirring at 40°C for 5 hours, and add 5lO2
An ethyl silicate partial hydrolysis condensation solution of about 15 cm was obtained.

製造例2(展色剤の製造) 攪拌機付容器にイソプロピルアルコール85部を入れ、
攪拌しながらこれにポリビニルブチラール((株)棟木
化学製、商品名[エスレックBL−1J )15部を少
量ずつ加え、均一になるまで攪拌して、有機樹脂溶液を
得た。
Production Example 2 (Production of color vehicle) Put 85 parts of isopropyl alcohol into a container equipped with a stirrer,
While stirring, 15 parts of polyvinyl butyral (manufactured by Muneki Kagaku Co., Ltd., trade name [S-LEC BL-1J) was added little by little, and the mixture was stirred until homogeneous to obtain an organic resin solution.

製造例1で得られたエチルシリケート縮合液、製造例2
で得られた有機樹脂溶液および?リアマイト樹脂硬化型
エポキシ樹脂(エポキシ樹脂ニジエル化学(株)エピコ
ート1004、ポリアマイド樹脂:富士化成(株)トー
マイド215X−70を80:20で用いた。)を展色
剤に用い第1表に示すとお9実施例1〜11および比較
例1〜9の乾量塗膜成分になるように塗料を作成し、屋
外曝露にて防錆性を炭酸ガス溶接及び重力式浴接にて溶
接性をテストした。結果を第1表に示す。それぞれのテ
スト方法は、以下の要領に従った。なお塗料成分の数値
はすべて乾量基準で示す。
Ethylsilicate condensation liquid obtained in Production Example 1, Production Example 2
The organic resin solution obtained in and? Reamite resin curable epoxy resin (Epoxy resin Nigel Kagaku Co., Ltd. Epicoat 1004, polyamide resin: Fuji Kasei Co., Ltd. Tomide 215X-70 was used in a ratio of 80:20) was used as a color vehicle, and as shown in Table 1. 9 Paints were prepared to have the dry weight coating components of Examples 1 to 11 and Comparative Examples 1 to 9, and the rust prevention properties were tested by outdoor exposure, and the weldability was tested by carbon dioxide gas welding and gravity bath welding. . The results are shown in Table 1. Each test method followed the guidelines below. All values for paint components are shown on a dry weight basis.

〔防錆性試験〕[Rust prevention test]

縦300肺、横10100r厚さ12111111の鋼
板をショツトブラストしこれに実施例1〜11、比較例
1〜9の塗料組成物を15〜25μになるように塗装し
、屋外で4ケ月曝露させて錆の発生状態をASTM −
D610/5SPC−VIs217)錆発生標準板ト比
較し評価した。評価の基準は、ASTMの9点′以上を
◎、7〜8点を○、5〜6点をΔ、3〜4点を×、2点
以下を××で示した。
A steel plate with a length of 300mm and a width of 10100mm and a thickness of 12111111 was shot blasted, coated with the coating compositions of Examples 1 to 11 and Comparative Examples 1 to 9 to a thickness of 15 to 25μ, and exposed outdoors for 4 months. ASTM-
D610/5SPC-VIs217) Rust occurrence standard plate was compared and evaluated. The evaluation criteria were as follows: ASTM scores of 9' or higher are ◎, 7 to 8 points are ○, 5 to 6 points are Δ, 3 to 4 points are ×, and 2 or less points are XX.

〔溶接試験〕[Welding test]

縦5001111+!、横j5Qm、厚さ161111
1の鋼板、をショツトブラストし、これに実施例1〜1
1.比較例1〜9の塗料組成物を15〜25μになるよ
うに塗装し、7日間乾燥させたのち、下記試験例1.2
で溶接試験を行った。JIS Z 3104に示される
X線溶接検査による判定を行った。
Vertical 5001111+! , width j5Qm, thickness 161111
The steel plate of No. 1 was shot blasted, and Examples 1 to 1 were applied to it.
1. The coating compositions of Comparative Examples 1 to 9 were applied to a thickness of 15 to 25μ, dried for 7 days, and then tested in Test Example 1.2 below.
A welding test was conducted. Judgment was made by X-ray welding inspection as specified in JIS Z 3104.

(lン試験例り。(An example of a test.

溶接棒MG50D((株)神戸製鋼新製)を使用し、炭
酸ガスシールドアーク溶接法で水平隅肉溶接試験を行っ
た。
A horizontal fillet welding test was conducted using a welding rod MG50D (manufactured by Kobe Steel, Ltd.) using a carbon dioxide shielded arc welding method.

(2)試験例2゜ 溶接棒ゼロード27((株)神戸製鋼新製)を使用して
、重力式溶接法で水平隅肉溶接試験を行ったO 表1の結果から明らかなように、本発明の塗料組成物を
用いれば、炭酸ガス溶接及び重力式溶接を行った時のブ
ローホール発生が極めて少なく、しかも長期間にわたり
鋼板の発錆を防止することができる。
(2) Test Example 2 A horizontal fillet welding test was conducted using the gravity welding method using the welding rod Zerode 27 (manufactured by Kobe Steel, Ltd.). As is clear from the results in Table 1, this By using the coating composition of the invention, blowholes are extremely less likely to occur during carbon dioxide gas welding and gravity welding, and rusting of steel sheets can be prevented for a long period of time.

Claims (3)

【特許請求の範囲】[Claims] (1) 乾量基準で展色剤5〜20重量%及び亜鉛フレ
ーク15〜60重量%を含むことを特徴とする溶接性良
好な一次防錆塗料組成物。
(1) A primary anticorrosive paint composition with good weldability, characterized by containing 5 to 20% by weight of a color vehicle and 15 to 60% by weight of zinc flakes on a dry weight basis.
(2) 上記亜鉛フレークが最大長さ100 ’tr以
下、平均長径1.5〜30μ、平均厚み5μ以下、アス
ペクト比(長径/厚み)3以上である特許請求の範囲第
1項記載の一次防錆塗料組成物。
(2) The primary defense according to claim 1, wherein the zinc flakes have a maximum length of 100'tr or less, an average major axis of 1.5 to 30μ, an average thickness of 5μ or less, and an aspect ratio (major axis/thickness) of 3 or more. Rust paint composition.
(3) 上記亜鉛フレークが亜鉛フレーク製造時に用い
る有機系粉砕剤を亜鉛フレーク中に3重量%以下の量で
含む特許請求の範囲第1項及び第2項記載の一次防錆塗
料組成物。
(3) The primary anticorrosive coating composition according to claims 1 and 2, wherein the zinc flakes contain an organic pulverizing agent used in the production of zinc flakes in an amount of 3% by weight or less.
JP24088683A 1983-12-22 1983-12-22 Primary rust preventing coating material composition having good weldability Pending JPS60133072A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP24088683A JPS60133072A (en) 1983-12-22 1983-12-22 Primary rust preventing coating material composition having good weldability

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP24088683A JPS60133072A (en) 1983-12-22 1983-12-22 Primary rust preventing coating material composition having good weldability

Publications (1)

Publication Number Publication Date
JPS60133072A true JPS60133072A (en) 1985-07-16

Family

ID=17066155

Family Applications (1)

Application Number Title Priority Date Filing Date
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Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7201790B1 (en) * 2005-12-02 2007-04-10 Savin Ronald R Zinc flake coating composition
US7678184B2 (en) 2001-02-14 2010-03-16 Metal Coatings International Inc. Particulate metal alloy coating for providing corrosion protection
US7740947B2 (en) 2001-02-14 2010-06-22 Metal Coatings International Inc. Particulate metal alloy coating for providing corrosion protection
WO2014014063A1 (en) 2012-07-20 2014-01-23 中国塗料株式会社 Primary rust preventive coating composition and use thereof
CN104073142A (en) * 2014-06-20 2014-10-01 合肥长城制冷科技有限公司 Antirust composition for steel tubes

Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS516828A (en) * 1974-07-10 1976-01-20 Taiho Kogyo Co Ltd Kinzokumenno boshokushoriho oyobi boshokuzai
JPS5448831A (en) * 1977-09-26 1979-04-17 Sakai Chem Ind Co Ltd Rust preventive coating compound
JPS5460329A (en) * 1977-10-20 1979-05-15 Sakai Chem Ind Co Ltd Scaly zinc powder and coating compound containing it
JPS5528333A (en) * 1978-08-16 1980-02-28 Shoji Nishimura Coating composite
JPS55122807A (en) * 1979-03-15 1980-09-20 Sakai Chem Ind Co Ltd Production of scaly zinc powder
JPS5688416A (en) * 1979-12-20 1981-07-17 Dainippon Toryo Co Ltd Corrosion-preventive lining composition
JPS57198767A (en) * 1981-05-30 1982-12-06 Nippon Oil & Fats Co Ltd Modified inorganic zinc rich paint of ultra thick film type

Patent Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS516828A (en) * 1974-07-10 1976-01-20 Taiho Kogyo Co Ltd Kinzokumenno boshokushoriho oyobi boshokuzai
JPS5448831A (en) * 1977-09-26 1979-04-17 Sakai Chem Ind Co Ltd Rust preventive coating compound
JPS5460329A (en) * 1977-10-20 1979-05-15 Sakai Chem Ind Co Ltd Scaly zinc powder and coating compound containing it
JPS5528333A (en) * 1978-08-16 1980-02-28 Shoji Nishimura Coating composite
JPS55122807A (en) * 1979-03-15 1980-09-20 Sakai Chem Ind Co Ltd Production of scaly zinc powder
JPS5688416A (en) * 1979-12-20 1981-07-17 Dainippon Toryo Co Ltd Corrosion-preventive lining composition
JPS57198767A (en) * 1981-05-30 1982-12-06 Nippon Oil & Fats Co Ltd Modified inorganic zinc rich paint of ultra thick film type

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7678184B2 (en) 2001-02-14 2010-03-16 Metal Coatings International Inc. Particulate metal alloy coating for providing corrosion protection
US7740947B2 (en) 2001-02-14 2010-06-22 Metal Coatings International Inc. Particulate metal alloy coating for providing corrosion protection
US7201790B1 (en) * 2005-12-02 2007-04-10 Savin Ronald R Zinc flake coating composition
WO2014014063A1 (en) 2012-07-20 2014-01-23 中国塗料株式会社 Primary rust preventive coating composition and use thereof
KR20150013907A (en) 2012-07-20 2015-02-05 주고꾸 도료 가부시키가이샤 Primary rust preventive coating composition and use thereof
CN104073142A (en) * 2014-06-20 2014-10-01 合肥长城制冷科技有限公司 Antirust composition for steel tubes

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