JPS6241627B2 - - Google Patents

Info

Publication number
JPS6241627B2
JPS6241627B2 JP57068667A JP6866782A JPS6241627B2 JP S6241627 B2 JPS6241627 B2 JP S6241627B2 JP 57068667 A JP57068667 A JP 57068667A JP 6866782 A JP6866782 A JP 6866782A JP S6241627 B2 JPS6241627 B2 JP S6241627B2
Authority
JP
Japan
Prior art keywords
weight
pigment
primary
welding
deacidifying
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
JP57068667A
Other languages
Japanese (ja)
Other versions
JPS58185660A (en
Inventor
Shiro Shimatani
Ryoji Oda
Hajime Okamoto
Osamu Kawada
Masatoshi Tanaka
Koichi Saneto
Kenichi Hirabayashi
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.)
Nippon Paint Co Ltd
Mitsui Zosen KK
Original Assignee
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 Nippon Paint Co Ltd, Mitsui Zosen KK filed Critical Nippon Paint Co Ltd
Priority to JP6866782A priority Critical patent/JPS58185660A/en
Publication of JPS58185660A publication Critical patent/JPS58185660A/en
Publication of JPS6241627B2 publication Critical patent/JPS6241627B2/ja
Granted legal-status Critical Current

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  • Chemical Treatment Of Metals (AREA)

Description

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

本発明は一次防錆塗料組成物に関し、さらに詳
しくは、加工前の鋼板に塗装して、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。 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
をブ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、一次防錆塗料を塗装すること
が一般的に行なわれている。 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―リン酸系のウオツシ
ユプライマー、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ツチペイント、無機バ
インダー―高濃度亜鉛末系の無機ジンクリツチペ
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
ンクリツ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ジドアーク
溶接法に比べて溶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つた。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。 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、一
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(特開昭47―8122
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つた。 本発明の目的は、従来の一次防錆塗料組成物の
有する欠点をなくし、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。 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
せるためには、脱酸性顔料を用いてブローホール
の発生を積極的に抑制すると同時に、高温分解ガ
スの発生を抑制することが不可欠であることを見
出して本発明に到達した。 本発明は、ガスシールド溶接法を用いる鋼板に
塗装され、乾量基準で脱酸性顔料10〜80重量%、
金属塩類防錆顔料10〜30重量%、および灼熱減量
(不活性ガス中、800℃、1時間)が35〜60重量%
である展色剤5〜20重量%を含むことを特徴とす
る。 本発明において、必須成分としての脱酸性顔
料、金属塩類防錆顔料および展色剤以外に、所望
により体質顔料、着色顔料、各種添加剤等を添加
してもよい。これらの塗料組成物は、乾燥塗膜と
したときの灼熱減量(不活性ガス中、800℃、1
時間)が40重量%以下のものであることが好まし
い。 本発明に用いられる脱酸性顔料とは、高温時に
酸素と反応して重量の増加するもので、溶接時に
その脱酸効果によりビード部を清浄にし、ブロー
ホールの発生を減少させるものである。脱酸性顔
料としては、例えばフエロマンガン、フエロシリ
コン、フエロチタン、フエロクロム、フエロジン
ク、フエロアルミ、リン鉄、マンガン粉、亜鉛
末、アルミニウム粉、フエライト合金粉等が用い
られる。脱酸性顔料を多く用いる程、溶接時のブ
ローホールの発生は抑制されるが、乾燥塗膜中80
重量%を越えると実質的に塗膜の形成が難しい。
また10重量%より少なくなると溶接時のブローホ
ールの発生が効果的に抑制されなくなる。脱酸性
顔料としての亜鉛末は、防錆性が良好であるが、
無酸素条件では500〜900℃においてガス化してブ
ローホールの原因となる。その含有量が乾燥塗膜
中50重量%を越えるとその傾向が顕著になる。 本発明に用いる脱酸性顔料(金属粉)は電導性
もあり、亜鉛末の量が少なくても防錆性は良好で
あるが、さらに防食性を向上させるため、また亜
鉛末以外の脱酸性顔料のみでは防錆性が期待でき
ないため、本発明の組成物では金属塩類の防錆顔
料を含有させている。これらの防錆顔料として
は、例えばリン酸亜鉛、リン酸アルミニウム、ジ
ンククロメート等の公知のものが用いられる。一
般的に防錆顔料は水親和性が高く、結晶水または
吸着水を含むため、その添加量は10〜30重量%が
適当であり30重量%を越えると溶接時にブローホ
ールが多く発生し、また10重量%より少ない場合
には防錆性が不充分となる。 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必要があり、かつその
使用量も少ない程良好なガスシールド溶接性を示
す。展色剤としては、例えばアルキルシリケート
Si(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を、
所望によりさらにアルコール可溶性有機樹脂(例
えばポリビニルブチラール、ボリビニルアルコー
ル、ポリアクリル酸エステル等)を、SiO2/有
機樹脂固形分が重量比で100/0〜60/40の範囲
となるようにブレンドして用いる。本発明の組成
物中の展色剤(樹脂成分)の使用量は乾燥塗膜中
5〜20重量%の範囲であり、20重量%を越える
と、炭酸ガス溶接時のブローホール発生が多くな
り、また5重量%以下では塗膜結合性が弱く、実
質的に塗膜形成が難しくなる。 本発明の組成物は、これらの必須成分以外に公
知の顔料、添加剤等を含有していてもよいが、乾
燥塗膜の、不活性ガス中の灼熱減量が大きくなる
ものが多いので使用に際しては注意を要する。灼
熱減量の少ないものとしては、例えば体質顔料と
してクレー、マイカ、硫酸バリウム等があり、着
色顔料として弁柄、チタン白、亜鉛華等がある。 本発明の組成物は、乾燥塗膜の、不活性ガス
中、800℃、1時間の灼熱減量が40重量%以下、
特に30重量%以下であることが好ましい。不活性
ガス中の灼熱減量の原因は前述のように種々ある
が、本発明の組成物において、灼熱減量が40重量
%を越えると、炭酸ガス溶接時にブローホールの
発生が多くなる。 本発明の塗装組成物は、ブ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、長時間にわたり鋼板の発錆を防
止することができる。また従来の一次防錆塗料組
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。 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%は重
量部および重量%を意味する。 製造例1 (展色剤の製造) エチルシリケート(日本コルコート化学(株)製、
商品名「エチルシリケート40」)38部およびイソ
プロピルアルコール57部を撹拌機付容器に入れ、
充分混合し、40℃に保温しながら撹拌し、これに
0.1N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時間撹拌を
続けて、SiO2分約15%のエチルシリケート部分
加水分解縮合液を得た。 製造例2 (展色剤の製造) 撹拌機付容器にイソプロピルアルコール85部を
入れ、撹拌しながらこれにポリビニルブチラール
((株)積水化学製、商品名「エスレツクBL―1」)
15部を少量ずつ加え、均一になるまで撹拌して、
有機樹脂溶液を得た。 実施例1〜9および比較例1〜3 製造例1で得られたエチルシリケート縮合液お
よび製造例2で得られた有機樹脂溶液を展色剤と
して用い、第1表に示す脱酸性顔料、防錆顔料、
着色顔料および体質顔料をそれぞれ第1表に示す
配合割合で使用直前に混合して塗料組成物を得
た。
The present invention relates to a primary rust-preventing paint composition, and more particularly to a primary rust-preventing paint composition that is applied to a steel plate before processing and provides good weldability during gas shield welding. 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 blast or pickle raw materials before processing to remove mill scale and rust, and then apply a primary anti-corrosion paint. Conventionally, the primary anti-corrosion paints used are:
Polyvinyl butyral resin - phosphoric acid based wash primer, organic resin such as epoxy resin - organic zinc-rich paint based on high concentration zinc dust, inorganic binder - high concentration zinc dust based inorganic zinc-rich paint, etc. 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 gas welding, the cooling rate of the molten metal is faster than in shielded arc welding and submerged arc welding.
Steel plates coated with conventional primary anti-corrosion paints have the disadvantage of producing a large number of blowholes. 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. 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 primary anticorrosion paints (Japanese Patent Laid-Open No. 47-8122
Even if this method was applied to carbon dioxide gas welding, good weldability was not necessarily obtained. An object of the present invention is to provide a primary rust preventive paint composition that eliminates the drawbacks of conventional primary rust preventive paint compositions and provides good weldability, particularly during gas shield welding. As a result of intensive research to achieve this objective, the present inventors found that in order to reduce the occurrence of blowholes during carbon dioxide gas welding, it is necessary to actively suppress the occurrence of blowholes by using deacidifying pigments, and at the same time, to reduce the occurrence of blowholes during high-temperature decomposition. The present invention was achieved by discovering that it is essential to suppress the generation of gas. The present invention is coated on a steel plate using a gas shield welding method, and contains 10 to 80% by weight of deoxidizing pigment on a dry weight basis.
Metal salt anti-corrosion pigment 10-30% by weight and loss on ignition (in inert gas, 800°C, 1 hour) 35-60% by weight
It is characterized by containing 5 to 20% by weight of a color vehicle. In the present invention, in addition to the essential components of a deacidifying pigment, a metal salt anticorrosion pigment, and a color vehicle, extender pigments, coloring pigments, various additives, and the like may be added as desired. These coating compositions have a ignition loss (in inert gas, 800°C, 1
time) is preferably 40% by weight or less. The deacidifying pigment used in the present invention is one that reacts with oxygen at high temperatures and increases in weight, and its deoxidizing effect cleans the bead during welding and reduces the occurrence of blowholes. As the deacidifying pigment, for example, ferromanganese, ferrosilicone, ferrotitanium, ferrochrome, ferrozinc, ferroaluminum, iron phosphorus, manganese powder, zinc powder, aluminum powder, ferrite alloy powder, etc. are used. The more deacidifying pigments are used, the more the blowholes are suppressed during welding.
If the amount exceeds % by weight, it is substantially difficult to form a coating film.
Moreover, if it is less than 10% by weight, the generation of blowholes during welding will not be effectively suppressed. Zinc dust as a deacidifying pigment has good rust prevention properties, but
Under anoxic conditions, it gasifies at 500 to 900°C and causes blowholes. This tendency becomes noticeable when the content exceeds 50% by weight in the dry coating film. The deacidifying pigment (metal powder) used in the present invention has electrical conductivity and has good rust prevention even with a small amount of zinc dust. Since rust preventive properties cannot be expected with just the metal salt, the composition of the present invention contains a metal salt rust preventive pigment. As these antirust pigments, known ones such as zinc phosphate, aluminum phosphate, zinc chromate, etc. can be used. In general, anti-rust pigments have a high affinity for water and contain crystal water or adsorbed water, so the appropriate amount to add is 10 to 30% by weight; if it exceeds 30% by weight, many blowholes will occur during welding. Moreover, if it is less than 10% by weight, the rust prevention properties will be insufficient. As the color vehicle used in the present invention, it is necessary to use one that has a small loss on high-temperature ignition, and the smaller the amount used, the better the gas shield weldability will be. As a color vehicle, for example, alkyl silicate
A partially hydrolyzed condensate of Si(OR) 4 (in the formula, R means an ethyl group, a butyl group, a cellosolve, etc.),
If desired, an alcohol-soluble organic resin (for example, polyvinyl butyral, polyvinyl alcohol, polyacrylic ester, etc.) is further blended so that the weight ratio of SiO 2 /organic resin solids is in the range of 100/0 to 60/40. used. The amount of the color vehicle (resin component) used in the composition of the present invention is in the range of 5 to 20% by weight in the dry coating film, and if it exceeds 20% by weight, blowholes will occur more often during carbon dioxide gas welding. If the amount is less than 5% by weight, the coating film bonding property will be weak and coating film formation will become substantially difficult. The composition of the present invention may contain known pigments, additives, etc. in addition to these essential components, but since many of them increase the loss of the dried coating film on ignition in an inert gas, requires caution. Examples of those having a small loss on burning include extender pigments such as clay, mica, and barium sulfate, and coloring pigments such as Bengara, titanium white, and zinc white. The composition of the present invention has a ignition loss of 40% by weight or less in a dry coating film at 800°C for 1 hour in an inert gas,
In particular, it is preferably 30% by weight or less. As mentioned above, there are various causes of loss on ignition in an inert gas, but if the loss on ignition exceeds 40% by weight in the composition of the present invention, blowholes will occur more frequently during carbon dioxide gas welding. When the coating composition of the present invention is applied to areas from which mill scale and rust have been removed by blasting, pickling, etc., it is possible to prevent rust from forming on a steel plate for a long period of time. In addition, welding work can be performed with high efficiency without causing many blowholes during carbon dioxide gas welding unlike conventional primary rust-preventing paint compositions. Hereinafter, production examples, examples, and comparative examples of the composition of the present invention will be described. In addition, parts and % in the following examples mean parts by weight and weight %. Production Example 1 (Production of color vehicle) Ethyl silicate (manufactured by Nippon Colcoat Chemical Co., Ltd.)
Put 38 parts of the product name "Ethyl silicate 40" and 57 parts of isopropyl alcohol into a container equipped with a stirrer,
Mix thoroughly, stir while keeping warm at 40℃, and add
A mixture of 0.5 parts of 0.1N hydrochloric acid and 4.5 parts of water was added dropwise over 1 hour. After the dropwise addition was completed, stirring was continued at 40° C. for 5 hours to obtain an ethyl silicate partial hydrolysis condensate solution containing about 15% SiO 2 minutes. Production Example 2 (Production of color vehicle) Put 85 parts of isopropyl alcohol into a container equipped with a stirrer, and add polyvinyl butyral (manufactured by Sekisui Chemical Co., Ltd., trade name "Eslec BL-1") to it while stirring.
Add 15 parts little by little and stir until homogeneous.
An organic resin solution was obtained. Examples 1 to 9 and Comparative Examples 1 to 3 Using the ethyl silicate condensation liquid obtained in Production Example 1 and the organic resin solution obtained in Production Example 2 as color vehicles, the deacidifying pigments and anti-oxidants shown in Table 1 were used. rust pigment,
Coloring pigments and extender pigments were mixed in the proportions shown in Table 1 immediately before use to obtain coating compositions.

【表】【table】

【表】 試験例 1 縦300mm、横100mm、厚さ12mmの鋼板をシヨツト
ブラストし、これに実施例1〜9および比較例1
〜3の塗料組成物を15〜20ミクロンになるように
塗装し、屋外で曝露させて錆の発生状態を目視で
観察した。得られた結果を第2表に示す。 試験例 2 縦150mm、横500mm、厚さ16mmの鋼板をシヨトブ
ラストし、これに実施例1〜9および比較例1〜
3の塗料組成物を15〜25ミクロンになるように塗
装し、7日間乾燥したのち、炭酸ガス溶接法で水
平隅肉溶接を行なつた。 JISZ3104に示されるX線溶接検査による判定
を行なつた。得られた結果を第2表に示す。
[Table] Test Example 1 A steel plate with a length of 300 mm, a width of 100 mm, and a thickness of 12 mm was shot blasted, and Examples 1 to 9 and Comparative Example 1 were applied to it.
The paint compositions of No. 3 to 3 were applied to a thickness of 15 to 20 microns, exposed outdoors, and the state of rust generation was visually observed. The results obtained are shown in Table 2. Test Example 2 A steel plate with a length of 150 mm, a width of 500 mm, and a thickness of 16 mm was shot blasted, and Examples 1 to 9 and Comparative Examples 1 to
The coating composition No. 3 was applied to a thickness of 15 to 25 microns, and after drying for 7 days, horizontal fillet welding was performed using carbon dioxide gas welding. Judgment was made by X-ray welding inspection as specified in JISZ3104. The results obtained are shown in Table 2.

【表】【table】

【表】 この表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、長時間にわたり鋼板の発錆
を防止することができ、また炭酸ガス溶接も行な
つても、ブローホールの発生を低減させることが
できる。
[Table] As is clear from the results in this table, if the coating composition of the present invention is used, it is possible to prevent rust on steel plates for a long time, and even when carbon dioxide gas welding is performed, blowholes do not occur. occurrence can be reduced.

Claims (1)

【特許請求の範囲】 1 ガスシールド溶接法を用いる鋼板に塗装され
る塗料組成物であつて、乾量基準で脱酸性顔料10
〜80重量%、金属塩類防錆顔料10〜30重量%、お
よび灼熱減量(不活性ガス中、800℃、1時間)
が35〜60重量%である展色剤5〜20重量%を含む
ことを特徴とする一次防錆塗料組成物。 2 特許請求の範囲第1項において、展色剤は、
アルキルシリケート部分加水分解縮合物(C−
1)とアルコール可溶性有機樹脂(C−2)から
なり、(C−1)の灼熱残査/(C−2)の固形
分が100/0〜60/40(重量比)の範囲であるこ
とを特徴とする一次防錆塗料組成物。 3 特許請求の範囲第1項において、脱酸性顔料
は亜鉛末を0〜50重量%含むことを特徴とする一
次防錆顔料組成物。 4 特許請求の範囲第1項において、前記塗料組
成物の乾膜の灼熱減量が40重量%以下であること
を特徴とする一次防錆塗料組成物。
[Scope of Claims] 1. A coating composition to be applied to a steel plate using a gas shield welding method, which comprises a deacidifying pigment of 10% on a dry basis.
~80% by weight, metal salt anticorrosion pigment 10-30% by weight, and loss on ignition (800°C, 1 hour in inert gas)
1. A primary anticorrosive paint composition comprising 5 to 20% by weight of a color vehicle and 35 to 60% by weight. 2 In claim 1, the color vehicle is:
Alkyl silicate partially hydrolyzed condensate (C-
1) and an alcohol-soluble organic resin (C-2), and the solid content of (C-1) burning residue/(C-2) is in the range of 100/0 to 60/40 (weight ratio). A primary anticorrosive paint composition characterized by: 3. The primary antirust pigment composition according to claim 1, wherein the deacidifying pigment contains 0 to 50% by weight of zinc dust. 4. The primary anticorrosive coating composition according to claim 1, wherein the dry film loss on ignition of the coating composition is 40% by weight or less.
JP6866782A 1982-04-26 1982-04-26 Primary rust-resisting paint composition Granted JPS58185660A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP6866782A JPS58185660A (en) 1982-04-26 1982-04-26 Primary rust-resisting paint composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP6866782A JPS58185660A (en) 1982-04-26 1982-04-26 Primary rust-resisting paint composition

Publications (2)

Publication Number Publication Date
JPS58185660A JPS58185660A (en) 1983-10-29
JPS6241627B2 true JPS6241627B2 (en) 1987-09-03

Family

ID=13380288

Family Applications (1)

Application Number Title Priority Date Filing Date
JP6866782A Granted JPS58185660A (en) 1982-04-26 1982-04-26 Primary rust-resisting paint composition

Country Status (1)

Country Link
JP (1) JPS58185660A (en)

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH03188171A (en) * 1989-12-15 1991-08-16 Furukawa Electric Co Ltd:The Resin composition for anticorrosive material
US5260120A (en) * 1991-12-06 1993-11-09 Morton International, Inc. Two coat weldable primer for steel
KR100381719B1 (en) * 1995-12-29 2003-08-14 고려화학 주식회사 Water-soluble anticorrosive paint composition
JPH11116856A (en) * 1997-10-14 1999-04-27 Kobe Paint Kk Rustproofing coating composition
JP5372305B2 (en) * 2000-08-04 2013-12-18 新日鐵住金株式会社 Painted steel with excellent anti-corrosion paint and corrosion resistance
JP2002114944A (en) * 2000-10-04 2002-04-16 Shinto Paint Co Ltd Primary anticorrosive paint composition
EP1506982B1 (en) * 2003-08-15 2006-10-04 Hoden Seimitsu Kako Kenkyusho Co., Ltd. Chromium-free metal surface treatment agent

Also Published As

Publication number Publication date
JPS58185660A (en) 1983-10-29

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