JPS61257270A - Treatment of zinc film surface - Google Patents

Treatment of zinc film surface

Info

Publication number
JPS61257270A
JPS61257270A JP9830085A JP9830085A JPS61257270A JP S61257270 A JPS61257270 A JP S61257270A JP 9830085 A JP9830085 A JP 9830085A JP 9830085 A JP9830085 A JP 9830085A JP S61257270 A JPS61257270 A JP S61257270A
Authority
JP
Japan
Prior art keywords
zinc
resin
film surface
treatment
paint
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
JP9830085A
Other languages
Japanese (ja)
Other versions
JPH0366949B2 (en
Inventor
Tadahito Nishimura
西村 田人
Minoru Fukushima
稔 福島
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
Original Assignee
Nippon Paint 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 Nippon Paint Co Ltd filed Critical Nippon Paint Co Ltd
Priority to JP9830085A priority Critical patent/JPS61257270A/en
Publication of JPS61257270A publication Critical patent/JPS61257270A/en
Publication of JPH0366949B2 publication Critical patent/JPH0366949B2/ja
Granted legal-status Critical Current

Links

Abstract

PURPOSE:To obtain the superior sticking property and anti-corrosiveness against a zinc surface by coating the zinc-plated film surface with the paint composition containing a thermoplastic resin and an anti-corrosive pigment. CONSTITUTION:In the treatment of the zinc film surface, an ordinary temperature drying-type paint containing a thermoplastic polyamide and an anti-corrosive pigmentm, further compounding a hard resin as desired is coated on the zinc-plated film surface. In such a manner, the water-proof property and adhesive property of the film are remarkably improved by combining the polyamide resin with the anti-corrosive pigment, and more improvement is made by compounding the hard resin. Accordingly, the superior sticking property and anti-corrosiveness against the zinc surface can be obtained.

Description

【発明の詳細な説明】 技術分野 本発明は亜鉛メッキ被膜表面の処理方法に係り、さらに
詳しくは熱可塑性ポリアミド樹脂と防錆顔料を含み、所
望によりハードレジンを配してなる塗料組成物を亜鉛メ
ッキ被膜表面に適用し亜鉛面゛に対しての優れた付着性
と防食性を得ることを目的とした亜鉛被膜表面の処理方
法に関するものである。
DETAILED DESCRIPTION OF THE INVENTION Technical Field The present invention relates to a method for treating the surface of a galvanized coating. The present invention relates to a method for treating the surface of a zinc coating, which is applied to the surface of a plating coating and is intended to obtain excellent adhesion and anticorrosion properties to the zinc surface.

従来技術 鉄鋼材あるいは鉄鋼製品の長期防食方法として亜鉛メッ
キやジンクリッチ塗料による塗装が侭行なわれ、また送
電鉄塔を中心とした大型構造物には溶融亜鉛メッキ被覆
がなされている。こういった亜鉛面は水や大気により消
耗されるのでそれを防ぐため、通常油性系塗料や合成樹
脂塗料が適用されている。
BACKGROUND OF THE INVENTION As a long-term corrosion protection method for steel materials or steel products, galvanizing or painting with zinc-rich paints has been used, and large structures such as power transmission towers are coated with hot-dip galvanizing. These zinc surfaces are consumed by water and the atmosphere, so to prevent this, oil-based paints or synthetic resin paints are usually applied.

しかしながら油性系塗料は亜鉛と反応して金属石ケンを
生成し、塗膜の早期剥離を招く欠点がある。ブチラール
樹脂を主成分とするウォッシュプライマー塗料での処理
は、湿度、乾燥時間、膜厚など塗装時の条件により付着
力が異なり安定な処理となり得ない。
However, oil-based paints have the disadvantage that they react with zinc to form metal soaps, leading to early peeling of the paint film. Treatment with a wash primer paint whose main component is butyral resin cannot be a stable treatment as the adhesion strength varies depending on conditions during painting such as humidity, drying time, and film thickness.

塩化ゴム塗料の塗装は比較的優れた効、果を与え。Painting with chlorinated rubber paint gives relatively good effects.

るが非メツキ部の鉄鋼材に接する部分で塩化ゴムの脱塩
酸による鉄鋼腐食が問題となる。アミン硬化のエポキシ
塗料ではかかる問題はないが、しかし2液型塗料である
点と低温時の乾燥不良で取り扱い上の不満を有する。こ
のように亜鉛メッキ被膜の処理方法として提案されてき
た技術はいづれも問題があり容易且つ確実な処理方法が
求められている。
However, steel corrosion due to dehydrochlorination of chlorinated rubber becomes a problem in the non-plated parts that come into contact with steel materials. Amine-cured epoxy paints do not have such problems, but they are dissatisfied with handling because they are two-component paints and dry poorly at low temperatures. As described above, all of the techniques that have been proposed as methods for treating galvanized coatings have problems, and there is a need for an easy and reliable treatment method.

発明が解決しようとする問題点 従って、亜鉛メッキ被膜に対し優れた付着力を有し、亜
鉛と反応することがなく、しかも非メツキ部の鉄面に対
しても優れた防食性を示す塗料で、乾燥性、可撓性も良
好なものを用い亜鉛メッキ面の防食目的での簡単な処理
方法を得ることが本発明目的である。
Problems to be Solved by the Invention Therefore, we have created a paint that has excellent adhesion to galvanized coatings, does not react with zinc, and also exhibits excellent anti-corrosion properties even on unplated iron surfaces. It is an object of the present invention to provide a simple treatment method for preventing corrosion of galvanized surfaces by using a material that has good drying properties and flexibility.

問題点を解決するための手段 本発明に従えば上記目的が亜鉛メッキ被膜表面に熱可塑
性ポリアミドと防錆顔料を含み、所望によりハードレジ
ンを配合してなる常温乾燥型塗料を塗装することを特徴
とする亜鉛メッキ被膜表面の処理方法により達成せられ
る。
Means for Solving the Problems According to the present invention, the above object is characterized in that the surface of the galvanized film is coated with a room-temperature-drying paint containing thermoplastic polyamide and anti-corrosion pigments, and optionally containing hard resin. This can be achieved by a method for treating the surface of a galvanized coating.

本発明で用いられる熱可塑性ポリアミド樹脂はポリカル
ボン酸とポリアミンの縮合物で分子量が4000〜12
000と比較的低く、軟化点80〜150℃、酸価10
以下、アミン価8以下の熱可塑性ポリアミドとして知ら
れる常温で固体の樹脂であり、例えばパーサミド930
.94o(ヘンケル白水):パーサロン111フ、11
29.1128、DPXJ50.DPX802.830
(ヘンケル白水);サンマイド550’−D、553、
HT140E(三相化学)等各種の市販品があり、それ
らがいづれも好適に使用せられる。
The thermoplastic polyamide resin used in the present invention is a condensate of polycarboxylic acid and polyamine, and has a molecular weight of 4,000 to 12
000, relatively low, softening point 80-150℃, acid value 10
The following refers to a resin that is solid at room temperature and is known as a thermoplastic polyamide with an amine value of 8 or less, such as Persamide 930.
.. 94o (Henkel Hakusui): Parsalon 111f, 11
29.1128, DPXJ50. DPX802.830
(Henkel Hakusui); Sanmide 550'-D, 553,
There are various commercially available products such as HT140E (Sanso Kagaku), and any of them can be suitably used.

本発明者らは上記ポリアミド樹脂が防錆顔料と組み合さ
れた場合、極めて予想外にも耐水性、付着性の改善され
た被膜を与え、特にハードレジンを配合した場合、耐水
性、付着性のより一層の改善が得られ1.メッキ部、非
メツキ部共に優れた耐食性を与えうろことを見出した。
The present inventors have found that when the above polyamide resin is combined with anti-corrosion pigments, it very unexpectedly provides a film with improved water resistance and adhesion, and especially when hard resin is blended, the water resistance and adhesion are improved. A further improvement in 1. We have discovered scales that provide excellent corrosion resistance in both plated and non-plated areas.

防錆顔料としては通常重防食用に使用せられる任意の防
錆顔料が用いられ、例えば鉛丹、シアナミド鉛、シアナ
ミド亜鉛、シンクロメート、ストロンチウムクロメート
、リン酸亜鉛、トリポリリン酸アルミニウム、三塩基性
硫酸鉛、亜酸化鉛、シアナミドカルシウム亜鉛、モリブ
デン酸アルミニウム、塩基性クロム酸鉛等の金属化合物
が有利に用いられる。
As the rust preventive pigment, any rust preventive pigment that is normally used for heavy duty corrosion protection is used, such as red lead, cyanamide lead, cyanamide zinc, synchromate, strontium chromate, zinc phosphate, aluminum tripolyphosphate, and tribasic sulfuric acid. Metal compounds such as lead, zinc oxide, calcium zinc cyanamide, aluminum molybdate, basic lead chromate are advantageously used.

本発明の好ましい態様として、上記成分と共に用いられ
るハードレジンは業界で知られた軟化点100″c′h
i後の常温で固形のハードレジン、例えばアルキルフェ
ノール、クマロンインデン樹脂、ロジンエステル、重合
ロジン、テルペン樹脂、エステルガム、フェノール樹脂
等である。
In a preferred embodiment of the present invention, the hard resin used with the above components has a softening point of 10"c'h as known in the industry.
Examples of hard resins that are solid at room temperature after i.

本発明で用いられるポリアミド樹脂、防錆顔料および所
望により加えられるハードレジンからなる塗料組成物に
は尚塗料用溶剤、顔料(着色顔料、体質顔料)等が添加
され、亜鉛メッキ被膜表面に対し常法、例えばエアレス
塗装法で適用され、常温乾燥により防錆塗装せられる。
A paint solvent, pigments (coloring pigments, extender pigments), etc. are added to the coating composition used in the present invention, which consists of a polyamide resin, a rust-preventing pigment, and a hard resin added as desired. It is applied by a method such as an airless coating method, and the anti-rust coating is applied by drying at room temperature.

前記組成物の樹脂ビヒクルはポリアミド樹脂のみから構
成せしめることができ、またハードレジンを配合する場
合、ポリアミド樹脂を樹脂成分の50%以上とすること
が好ましい。しかしながら後者においてはポリアミド樹
脂を全樹脂量の30%以上用いることにより本発明目的
を達成することができる。
The resin vehicle of the composition can be composed only of polyamide resin, and when hard resin is blended, it is preferable that the polyamide resin accounts for 50% or more of the resin component. However, in the latter case, the object of the present invention can be achieved by using polyamide resin in an amount of 30% or more of the total resin amount.

本発明の処理方法に於てはこのようにポリアミド樹脂を
主ビヒクルとした塗料が用いられ、該樹脂はエステル結
合を含まぬため亜鉛石ケンを生成することがないし、ま
た脱塩酸等の分解もなく、安定な樹脂であるため非メツ
キ部の鉄面にも適用が可能である。またポリアミド樹脂
は鉄面、亜鉛メッキ面に対し特に優れた付着性を示し、
Tgが低く可撓性に富むため被塗物変形への付着追随が
容易である特徴をもち、防錆顔料の併用により優れた耐
食性を示す。
In this way, in the treatment method of the present invention, a paint containing polyamide resin as the main vehicle is used, and since the resin does not contain ester bonds, it does not generate zinc soap, and it is also resistant to decomposition such as dehydrochlorination. Since it is a stable resin, it can also be applied to unplated steel surfaces. In addition, polyamide resin exhibits particularly excellent adhesion to iron and galvanized surfaces.
Because it has a low Tg and is highly flexible, it can easily adhere to the deformation of the object to be coated, and when used in combination with a rust-preventing pigment, it exhibits excellent corrosion resistance.

従って本発明は亜鉛、亜鉛メッキ面、ジンクリッチペイ
ント塗面に対し、優れた保護ならびに防食効果を発揮し
、技術水準を一段と進歩せしめるものであって産業上極
めて有用な発明を構成する。
Therefore, the present invention exhibits excellent protection and anticorrosion effects on zinc, galvanized surfaces, and zinc-rich paint coated surfaces, further advances the state of the art, and constitutes an extremely useful invention industrially.

以下実施例により本発明を説明する。特にことわりなき
限り、部ならびに%は重量による。
The present invention will be explained below with reference to Examples. Parts and percentages are by weight unless otherwise specified.

実施例1 下記配合により防食塗料N o、 1を常法に従い作っ
た。
Example 1 Anticorrosive paint No. 1 was prepared according to the conventional method using the following formulation.

重量部 DPX−550’7ニス 1)     24ヒタノー
ル1002ワニス 2)24 シアナミド鉛           10タ  ル  
り                        
15り  し  −                
        15キジロール          
   9イソプロピルアルコール       3合 
 計     100 注1)DPX−550(ポリアミド樹脂、ヘンケル白水
社製、アミン価1、酸価3、軟化点100℃)の50%
溶液、溶剤、キジロール/イソプロパノ−ルー3/1 2)ヒタノール1002(アルキルフェノール樹脂、日
立化成製)の50%溶液、溶剤キシロール/イソプロパ
ノ−ルー3/1 上記塗料を溶融亜鉛メッキ鋼板(J l5−G−300
25PG2G)および(J l5−G−33025PG
3S)にエステル塗装法により60〜70μになるよう
塗装し、数日間風乾させた。
Weight part DPX-550'7 Varnish 1) 24 Hytanol 1002 Varnish 2) 24 Cyanamide Lead 10 Tal
the law of nature
15 risi -
15 pheasant roll
9 isopropyl alcohol 3 cups
Total 100 Note 1) 50% of DPX-550 (polyamide resin, manufactured by Henkel Hakusui Co., Ltd., amine value 1, acid value 3, softening point 100°C)
Solution, solvent, xylol/isopropanol 3/1 2) 50% solution of Hytanol 1002 (alkylphenol resin, manufactured by Hitachi Chemical), solvent xylol/isopropanol 3/1 -300
25PG2G) and (J l5-G-33025PG
3S) by the ester coating method to a thickness of 60 to 70μ, and air-dried for several days.

実施例2 実施例1と同様方法を下記組成の防食塗料No。Example 2 The same method as in Example 1 was applied to anticorrosive paint No. of the following composition.

2を用い実施した。2 was used.

サンマイド5500ワニス 3)24 エステルガム105ワニズ 4)24 リン酸亜鉛ZP−8B  S>     10タ  ル
  り                      
  15り  し  −              
         15キシO−ル         
    9イソプロパツール          3合
  計       100 注3)アミン価3〉、酸fiii7>、軟化点110℃
のポリアミド樹脂、三相化学社製の50%(キジロール
/イソプロパノ−ルー3/1)の溶液。
Sanmide 5500 Varnish 3) 24 Ester Gum 105 Varnish 4) 24 Zinc Phosphate ZP-8B S> 10 Talli
15 risi -
15xO-l
9 Isopropanol 3 Total 100 Note 3) Amine value 3>, acid fiii7>, softening point 110°C
polyamide resin, 50% (Kijirol/Isopropanol 3/1) solution manufactured by Sanso Kagaku Co., Ltd.

4)エステルガム、荒用工業社製の50%(キシロール
/イソプロパノ−ルー3/1)溶液。
4) Ester gum, 50% (xylol/isopropanol 3/1) solution manufactured by Arayo Kogyo Co., Ltd.

5)菊池色素社製 実施例3 実施例1と同様方法を下記組成の防食塗料No。5) Manufactured by Kikuchi Color Co., Ltd. Example 3 The same method as in Example 1 was applied to anticorrosive paint No. of the following composition.

3を用い実施した。It was carried out using 3.

DPX−550ワニス      48LFボ一セイP
M3000 6)  10タ  ル  り      
                15り  し  −
                        1
5キジロール             9イソプロパ
ツール          3合  計       
100 注6)菊池色素工業社製 比較例1〜3 実施例1と同様方法を下記塗料組成物を用い実施した。
DPX-550 Varnish 48LF Bossei P
M3000 6) 10 tal
15 risi -
1
5 Kijirol 9 Isopropanol 3 Total
100 Note 6) Manufactured by Kikuchi Color Industries, Ltd. Comparative Examples 1 to 3 The same method as in Example 1 was carried out using the following coating composition.

比較例I  DPX−55048 タ  ル  り            25り  し
  −            15キジロール   
    9 イソプロパツール    3 比較例2 ウォッシュプライマー(ビニレックスアクチブプライマ
ーa/p110日本ペイ ント■) JIS−に−56272種A(FZプ5イマ一 日本ペ
イント■) 比較例3 エポキシプライマー(ハイボン20 エース 日本ペイント@) 上記処理のほどこされた各亜鉛メッキ鋼板につき下記の
ごとき試験を実施し、この結果を第1表に示した。
Comparative Example I DPX-55048 Taruri 25 Rishi - 15 Kijiroll
9 Isopropanol 3 Comparative Example 2 Wash Primer (Vinyrex Active Primer A/P110 Nippon Paint ■) JIS-Ni-56272 Type A (FZ Pu5 Imaichi Nippon Paint ■) Comparative Example 3 Epoxy Primer (Hibon 20 Ace Nippon Paint @) The following tests were carried out on each of the galvanized steel sheets subjected to the above treatment, and the results are shown in Table 1.

付着性・・・塗膜に5×51のゴバン目4個を素地に達
するように切り込みゴバン目に粘着セロファンテープを
貼りつけてからテープをはがした際の状態を調べた。
Adhesion: Four 5 x 51 squares were cut into the paint film to reach the substrate, adhesive cellophane tape was pasted on the squares, and the condition was examined when the tape was removed.

(A)塩水噴霧試験 500時間後の付着性(B)20
℃水道水浸漬 30日後の付着性(C)結露試験 出端
式発露試験機を用い30℃、50℃の温度サイクル(2
時間毎) 1000時間後の付着 (D)自然バクロ 1ケ年後の付着性 (E)屈曲性 J Is−に−5400により屈曲性を
評価、径10Illで実施 良好・・・O不良・・・× (以下余白) 手続補正書(自発) 昭和60年12月5日
(A) Adhesion after 500 hours of salt spray test (B) 20
℃ Tap water immersion Adhesion after 30 days (C) Dew condensation test Temperature cycle of 30℃ and 50℃ (2
(hourly) Adhesion after 1000 hours (D) Natural backlash Adhesion after 1 year (E) Flexibility Flexibility was evaluated by J Is-5400, good performance with diameter 10Ill...O poor... × (blank space below) Procedural amendment (voluntary) December 5, 1985

Claims (1)

【特許請求の範囲】[Claims] 亜鉛メッキ被膜表面に熱可塑性ポリアミドと防錆顔料を
含み所望によりハードレジンを配合してなる常温乾燥型
塗料を塗装することを特徴とする亜鉛メッキ被膜表面の
処理方法。
A method for treating the surface of a galvanized coating, which comprises applying a room temperature drying paint containing a thermoplastic polyamide and an anti-corrosion pigment and optionally a hard resin to the surface of the galvanized coating.
JP9830085A 1985-05-09 1985-05-09 Treatment of zinc film surface Granted JPS61257270A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP9830085A JPS61257270A (en) 1985-05-09 1985-05-09 Treatment of zinc film surface

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP9830085A JPS61257270A (en) 1985-05-09 1985-05-09 Treatment of zinc film surface

Publications (2)

Publication Number Publication Date
JPS61257270A true JPS61257270A (en) 1986-11-14
JPH0366949B2 JPH0366949B2 (en) 1991-10-21

Family

ID=14216066

Family Applications (1)

Application Number Title Priority Date Filing Date
JP9830085A Granted JPS61257270A (en) 1985-05-09 1985-05-09 Treatment of zinc film surface

Country Status (1)

Country Link
JP (1) JPS61257270A (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101772565B (en) * 2007-08-10 2015-03-18 日本能源株式会社 Surface-treating agent, surface treatment method, and mechanical component

Also Published As

Publication number Publication date
JPH0366949B2 (en) 1991-10-21

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