JP2721292B2 - Aluminum-zinc alloy coated steel sheet treated with organic surface treatment agent - Google Patents

Aluminum-zinc alloy coated steel sheet treated with organic surface treatment agent

Info

Publication number
JP2721292B2
JP2721292B2 JP4300107A JP30010792A JP2721292B2 JP 2721292 B2 JP2721292 B2 JP 2721292B2 JP 4300107 A JP4300107 A JP 4300107A JP 30010792 A JP30010792 A JP 30010792A JP 2721292 B2 JP2721292 B2 JP 2721292B2
Authority
JP
Japan
Prior art keywords
resin
aluminum
zinc alloy
steel sheet
plated steel
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 - Fee Related
Application number
JP4300107A
Other languages
Japanese (ja)
Other versions
JPH06146001A (en
Inventor
俊一 丸
敏夫 木屋
芳彦 保母
博 福留
尚孝 植田
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 Steel Corp
Asahi Kagaku Kogyo Co Ltd
Original Assignee
Sumitomo Metal Industries Ltd
Asahi Kagaku Kogyo 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 Sumitomo Metal Industries Ltd, Asahi Kagaku Kogyo Co Ltd filed Critical Sumitomo Metal Industries Ltd
Priority to JP4300107A priority Critical patent/JP2721292B2/en
Publication of JPH06146001A publication Critical patent/JPH06146001A/en
Application granted granted Critical
Publication of JP2721292B2 publication Critical patent/JP2721292B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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  • Laminated Bodies (AREA)
  • Paints Or Removers (AREA)
  • Chemical Treatment Of Metals (AREA)

Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【産業上の利用分野】本発明は、有機表面処理剤によっ
て処理されたアルミニウム−亜鉛合金めっき鋼板に関す
る。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to an aluminum-zinc alloy plated steel sheet treated with an organic surface treating agent.

【0002】[0002]

【従来の技術】アルミニウム−亜鉛合金めっき鋼板は、
アルミニウムが4〜75重量%残りの大半が亜鉛、さら
にSi,Mg,Ce−La(ミッシュメタル)など第3
成分が微量添加された合金によってめっきされた鋼板で
ある。
2. Description of the Related Art Aluminum-zinc alloy-plated steel sheets are:
Aluminum is 4 to 75% by weight. Most of the remaining is zinc, and third is Si, Mg, Ce-La (Misch metal).
It is a steel plate plated with an alloy to which components are added in trace amounts.

【0003】現在、製品化されている物は、アルミニウ
ムが4〜10重量%、Mg,Ce−Laを約0.1重量
%、残部が亜鉛から成る合金をめっきした低アルミニウ
ム−亜鉛合金めっき鋼板と、アルミニウムを55重量
%、亜鉛を43.4重量%、Siを1.6重量%配合し
た合金をめっきした高アルミニウム−亜鉛合金めっき鋼
板との2種類がある。そして、耐食性に関しては、従来
の溶融亜鉛めっき鋼板と同一めっき厚みで比較して、低
アルミニウム−亜鉛合金めっき鋼板で1.5〜2倍、高
アルミニウム−亜鉛合金めっき鋼板では3〜6倍の耐食
性に優れた性質を有する。この優れた耐食性から、屋根
材、壁材などの建材製品、ガードレール、防音壁、排水
溝などの土木製品の材料、自転車、家電製品、産業機器
などの材料、さらには塗装鋼板の基板などとして幅広く
使用されている。しかしながら、アルミニウム−亜鉛合
金めっき鋼板においては、そのめっき層にはアルミニウ
ムが配合されているため、特に、高アルミニウム−亜鉛
合金めっき鋼板では、従来の亜鉛めっき鋼板と比較し
て、以下のような問題が存在する。
At present, low-aluminum-zinc alloy-plated steel sheets plated with an alloy comprising 4 to 10% by weight of aluminum, about 0.1% by weight of Mg and Ce-La, and the balance being zinc are commercially available. And a high aluminum-zinc alloy plated steel sheet plated with an alloy containing 55% by weight of aluminum, 43.4% by weight of zinc, and 1.6% by weight of Si. As for the corrosion resistance, when compared with the conventional hot-dip galvanized steel sheet with the same plating thickness, the corrosion resistance of the low aluminum-zinc alloy coated steel sheet is 1.5 to 2 times, and that of the high aluminum-zinc alloy coated steel sheet is 3 to 6 times. It has excellent properties. Due to this excellent corrosion resistance, it is widely used as a building material product such as roofing material and wall material, a material for civil engineering products such as guardrails, soundproof walls, drainage ditches, a material for bicycles, home appliances, industrial equipment, etc., and a substrate of painted steel plate. It is used. However, in aluminum-zinc alloy-plated steel sheets, since the plating layer contains aluminum, the following problems, especially in high aluminum-zinc alloy-plated steel sheets, compared to conventional galvanized steel sheets. Exists.

【0004】(1)めっきしたままの状態で湿潤環境下
におかれると、亜鉛めっき鋼板よりは少ないが発錆す
る。錆が亜鉛めっき鋼板では白色であるが、アルミニウ
ム−亜鉛合金めっき鋼板では灰色から黒色であり、めっ
き表面が黒変し、著しく商品価値が低下する。これを解
決するために従来は、アルミニウム−亜鉛合金めっき層
の上にクロメート処理を行っている。
(1) When placed in a humid environment while being plated, rust is generated although the amount is smaller than that of a galvanized steel sheet. The rust is white in the galvanized steel sheet, but is gray to black in the aluminum-zinc alloy plated steel sheet, the plating surface is blackened, and the commercial value is significantly reduced. In order to solve this, conventionally, a chromate treatment is performed on the aluminum-zinc alloy plating layer.

【0005】(2)従来の溶融亜鉛めっき鋼板と比較し
て、めっき被膜が硬く、ロール成形やプレス成形を行っ
て加工する際に、潤滑性が悪く、めっき層が破壊された
り、摩擦熱によってめっき層が成形ロールやプレス金型
に融着する現象を生じたりする。この結果、アルミニウ
ム−亜鉛合金めっき鋼板から出る金属粉末が成形ロール
やプレス金型に付着することになり、成形品のコーナ部
分にこの金属粉末がたまって焼付き現象を生じたり、傷
やアブレージョンなどの欠陥を生じたりして外観変化が
発生する。これを解決するために従来は、アルミニウム
−亜鉛合金めっき鋼板の表面に油やワックスなどの潤滑
剤を塗布している。しかし、アルミニウム−亜鉛合金め
っき鋼板を屋根材として使用するときは、施工時に足を
滑らせる危険性があり、またこの上に塗装を施す場合を
考えて出荷時に潤滑剤を完全に除去しなければならな
い。このような潤滑剤の塗布と除去の手間を省略するた
めに、アクリル系樹脂でアルミニウム−亜鉛合金めっき
鋼板の表面を被覆する方法が提案されている。そしてこ
の方法では、同時にアクリル系樹脂にクロム酸を添加す
ることによって(1)に述べたクロメート処理に代える
こともできる(特公平1ー53353、特公平4ー26
72)。
(2) Compared with the conventional hot-dip galvanized steel sheet, the coating film is harder and has poor lubricity when processed by roll forming or press forming. A phenomenon that the plating layer is fused to a forming roll or a press die may occur. As a result, the metal powder from the aluminum-zinc alloy-plated steel sheet adheres to the forming rolls and press dies, and the metal powder accumulates at the corners of the formed product, causing seizure, scratches, abrasion, etc. Or a change in appearance. Conventionally, a lubricant such as oil or wax is applied to the surface of an aluminum-zinc alloy-plated steel sheet to solve this problem. However, when using aluminum-zinc alloy-plated steel sheets as roofing materials, there is a danger of slipping during construction, and in consideration of applying paint on this, the lubricant must be completely removed before shipping. No. In order to eliminate the trouble of applying and removing such a lubricant, a method of coating the surface of an aluminum-zinc alloy-plated steel sheet with an acrylic resin has been proposed. In this method, the chromate treatment described in (1) can be replaced by simultaneously adding chromic acid to the acrylic resin (Japanese Patent Publication No. 1-53353, Japanese Patent Publication No. 4-26).
72).

【0006】[0006]

【発明が解決しようとする課題】しかしながら、アルミ
ニウム−亜鉛合金めっき鋼板の用途が拡がり、屋根材、
壁材などの建材製品、ガードレール、防音壁、排水溝な
どの土木製品に使用された場合、スレート、コンクリー
トなどのアルカリ金属またはアルカリ土金属を含む材料
と接触することが多くなり、これらからアルカリ成分が
溶出し、アルミニウム−亜鉛合金めっき鋼板の表面がア
ルカリ成分の影響を受け著しく黒変し、外観が劣化し、
激しい場合は使用不能になる。
However, the use of aluminum-zinc alloy-plated steel sheets has expanded, and
When used in construction products such as wall materials, civil engineering products such as guardrails, soundproof walls, drains, etc., they often come into contact with materials containing alkali metals or alkaline earth metals such as slate and concrete, and from these, alkali components Elutes, the surface of the aluminum-zinc alloy-plated steel sheet is significantly blackened by the influence of the alkali component, and the appearance is deteriorated,
If it is severe, it will be unusable.

【0007】本発明の目的は、耐アルカリ性を有し、そ
の上湿潤環境下での耐黒錆性(耐食性)と、潤滑性とを
有するアルミニウム−亜鉛合金めっき鋼板を提供するも
のである。
An object of the present invention is to provide an aluminum-zinc alloy-plated steel sheet having alkali resistance, black rust resistance (corrosion resistance) in a humid environment, and lubricity.

【0008】[0008]

【課題を解決するための手段】本発明は、水分散性もし
くは水溶性ポリエステル樹脂または水分散性もしくは水
溶性ポリウレタン樹脂の1種または2種以上の混合物を
含む樹脂分と、前期樹脂分に対し、6価クロムを30%
以上含むクロム化合物を、酸化クロム換算で0.1〜5
%とを配合した樹脂組成物を、アルミニウム−亜鉛合金
めっき鋼板の表面に0.3〜4g/m2 の乾燥重量の厚
さで塗布したことを特徴とする有機表面処理剤で処理さ
れたアルミニウム−亜鉛合金めっき鋼板である。
SUMMARY OF THE INVENTION The present invention relates to a resin containing one or a mixture of two or more of a water-dispersible or water-soluble polyester resin or a water-dispersible or water-soluble polyurethane resin; 30% hexavalent chromium
The chromium compound containing above is 0.1 to 5 in terms of chromium oxide.
% Of the aluminum-zinc alloy-coated steel sheet is applied to the surface of the aluminum-zinc alloy-plated steel sheet at a dry weight of 0.3 to 4 g / m 2. -Zinc alloy plated steel sheet.

【0009】[0009]

【0010】[0010]

【0011】[0011]

【0012】また本発明は、前記樹脂組成物が、ガラス
転移温度40℃以上の樹脂とガラス転移温度40℃未満
の樹脂とを、そのクロム酸化合物を除いた乾燥重量比で
95:5〜50:50の割合で含む混合物であることを
特徴とする。
Further, the present invention provides a resin composition comprising a resin having a glass transition temperature of 40 ° C. or more and a resin having a glass transition temperature of less than 40 ° C. in a dry weight ratio excluding a chromic acid compound of 95: 5 to 50. : 50 is a mixture containing at a ratio of 50.

【0013】さらにまた本発明は、前記樹脂組成物が、
さらにオレフィン系ワックスを乾燥重量で0.1〜20
%含むことを特徴とする。
Further, the present invention provides the above-mentioned resin composition,
In addition, 0.1 to 20 parts by weight of olefin wax
%.

【0014】[0014]

【作用】本発明者らは鋭意研究し、耐アルカリ性に優
れ、湿潤環境下での耐食性と潤滑性にも優れた合成樹脂
被膜を有するアルミニウム−亜鉛合金めっき鋼板を得る
ことができた。合成樹脂被膜の性状は、樹脂の骨格、官
能基の種類、膜厚などに関係する。
The present inventors have conducted intensive studies and have obtained an aluminum-zinc alloy-plated steel sheet having a synthetic resin film having excellent alkali resistance and excellent corrosion resistance and lubricity in a humid environment. The properties of the synthetic resin film are related to the skeleton of the resin, the type of the functional group, the film thickness, and the like.

【0015】本発明に従えば、合成樹脂被膜を形成する
樹脂分としてポリエステル樹脂またはポリウレタン樹脂
が耐アルカリ性が良好であり、近年のVOC規制などの
観点から水分散性または水溶性であることが好ましい。
また樹脂の膜厚は、耐アルカリ性を考えれば厚い程よい
が、膜厚が厚い程乾燥、焼付きに時間がかかり、乾燥、
焼付きが不充分な場合は造膜が不充分になり、かえって
耐アルカリ性が劣り、高コストとなる。したがって、本
発明に用いる樹脂被膜量が0.3g/m2 (乾燥重量以
下同じ)で、従来例のアクリル系樹脂の1g/m2 と同
等またはそれ以上の耐食効果がある。まためっきや塗装
を従来と同一製造ラインで処理する場合、4g/m2
上とする必要はない。
According to the present invention, the polyester resin or the polyurethane resin as the resin component forming the synthetic resin film has good alkali resistance, and is preferably water-dispersible or water-soluble from the viewpoint of recent VOC regulations and the like. .
The thickness of the resin is preferably thicker in consideration of alkali resistance, but the thicker the film, the longer it takes to dry and seize.
Insufficient seizure results in insufficient film formation, rather poor alkali resistance and high cost. Therefore, the amount of the resin film used in the present invention is 0.3 g / m 2 (the same applies to the dry weight or less), and has a corrosion resistance effect equal to or more than 1 g / m 2 of the conventional acrylic resin. Further, when plating and painting are processed on the same production line as the conventional one, it is not necessary to make the amount more than 4 g / m 2 .

【0016】ポリエステル樹脂やポリウレタン樹脂は、
アクリル系樹脂と同等またはそれ以上の塗膜の潤滑性を
有し、アルミニウム−亜鉛合金めっき鋼板の表面を被覆
し、かつ完全に造膜するという意味で0.3〜4g/m
2 の範囲で良く、好ましくは性能とコストの面から0.
8〜1.5g/m2 でよい。さらに、特別な深絞り用途
に対しては、その加工性を容易にするために上記ポリエ
ステル樹脂またはポリウレタン樹脂被膜中に乾燥重量で
0.1〜20%のポリオレフィン系ワックスを添加する
ことが好ましい。ポリオレフィン系ワックスの添加量
は、0.1%以下では効果が小さく、また多いほど加工
性は向上するが20%を超えると耐食性、耐アルカリ性
が低下する。
The polyester resin and the polyurethane resin are
0.3 to 4 g / m in the sense of having a lubricity equivalent to or higher than that of an acrylic resin, covering the surface of an aluminum-zinc alloy-plated steel sheet, and completely forming a film.
2 is preferable, and is preferably 0. 0 in view of performance and cost.
It may be 8 to 1.5 g / m 2 . Further, for special deep drawing applications, it is preferable to add 0.1 to 20% by dry weight of a polyolefin-based wax to the polyester resin or polyurethane resin coating in order to facilitate the processability. When the amount of the polyolefin-based wax is 0.1% or less, the effect is small, and when the amount is large, the processability is improved, but when it exceeds 20%, the corrosion resistance and the alkali resistance are reduced.

【0017】合成樹脂被膜に耐食性を付与するために、
クロム酸化合物を配合することが必要である。アルミニ
ウム−亜鉛めっき鋼板上にクロメート処理をした後、ポ
リエステル系樹脂やポリウレタン系樹脂の被膜を施す方
法もあるが、実ラインを想定した場合、前記アルミニウ
ム−亜鉛合金めっき鋼板上にクロメート処理した後、樹
脂被膜を施す方法ではクロメート処理後の乾燥により鋼
帯の温度が上昇するため、樹脂の塗布管理が非常に難し
くなる。したがって、本発明ではアルミニウム−亜鉛め
っき鋼板に、クロメート処理をしないで、6価クロムを
配合した前記構成の樹脂分を塗布する。樹脂中の6価ク
ロムは焼付きけ時に1部3価クロムに還元される。本発
明の樹脂における6価クロムの全クロムに占める割合
は、30%以上である。本発明において、特に6価クロ
ムの溶出を防止する必要があるときはグリコールなどの
還元剤を使用し、樹脂被膜中の6価クロムの割合を30
%まで下げることも可能である。樹脂に添加するクロム
化合物の割合は、樹脂の固形分に対してCrO3 換算で
0.1〜5%が良い。CrO3 が0.1%より低いと充
分な耐食性が発現されない。また、5%より多いと耐ア
ルカリ性が低下するとともに、樹脂組成物の安定性が悪
くなる。本発明に使用するクロム化合物としては、Cr
3,K2CrO4 ,K2Cr27など6価クロム化合物
であれば特に限定されない。
In order to impart corrosion resistance to the synthetic resin film,
It is necessary to incorporate a chromic acid compound. After performing chromate treatment on an aluminum-zinc-plated steel sheet, there is also a method of applying a coating of a polyester-based resin or a polyurethane-based resin, but assuming a real line, after performing a chromate treatment on the aluminum-zinc alloy-plated steel sheet, In the method of applying a resin film, the temperature of the steel strip rises due to drying after the chromate treatment, so that it becomes very difficult to control the application of the resin. Therefore, according to the present invention, the aluminum-zinc plated steel sheet is not subjected to the chromate treatment, but is coated with the resin component having the above-described composition containing hexavalent chromium. The hexavalent chromium in the resin is reduced to one part trivalent chromium during burning. The proportion of hexavalent chromium in the total chromium in the resin of the present invention is 30% or more. In the present invention, particularly when it is necessary to prevent the elution of hexavalent chromium, a reducing agent such as glycol is used, and the proportion of hexavalent chromium in the resin film is reduced to 30%.
%. The ratio of the chromium compound to be added to the resin is preferably 0.1 to 5% in terms of CrO 3 with respect to the solid content of the resin. If CrO 3 is less than 0.1%, sufficient corrosion resistance is not exhibited. On the other hand, if it is more than 5%, the alkali resistance decreases and the stability of the resin composition deteriorates. The chromium compound used in the present invention is Cr
It is not particularly limited as long as it is a hexavalent chromium compound such as O 3 , K 2 CrO 4 , K 2 Cr 2 O 7 .

【0018】[0018]

【0019】本発明において使用するポリエステル樹脂
およびポリウレタン系樹脂は、その種類により樹脂被膜
硬度が異なる。被膜硬度が高いほど、平面での潤滑性能
は向上するが、加工すると加工部に微細なクラックが生
じるため、加工部での耐アルカリ性および耐食性が低下
する。したがって、本発明ではガラス転移温度(Tg)
が80〜40℃と高く、被膜硬度が高い樹脂とTgが、
40未満〜−10℃と低く被膜硬度の低い樹脂とを乾燥
重量比95:5〜50:50の範囲で混合して用いるこ
とが好ましい。一般に、Tgが低い樹脂は、平面での耐
アルカリ性、耐食性、潤滑性は劣るが、これによって平
面部、加工部の耐アルカリ性、耐食性、潤滑性に優れた
樹脂被膜となる。
The polyester resin and the polyurethane resin used in the present invention have different resin film hardness depending on the type. The higher the coating hardness, the better the lubricating performance on a flat surface, but when processed, fine cracks are generated in the processed part, so that the alkali resistance and corrosion resistance in the processed part are reduced. Therefore, in the present invention, the glass transition temperature (Tg)
Is as high as 80 to 40 ° C, and the resin and Tg with high coating hardness are
It is preferable that a resin having a low coating hardness of as low as less than 40 to -10 ° C is used in a dry weight ratio of 95: 5 to 50:50. In general, a resin having a low Tg is inferior in alkali resistance, corrosion resistance, and lubricity on a flat surface, but this results in a resin film excellent in alkali resistance, corrosion resistance, and lubricity of a flat portion and a processed portion.

【0020】[0020]

【実施例】以下、実施例でもって本発明をより具体的に
説明するが、本発明はこれに限定されるものではない。
EXAMPLES The present invention will be described in more detail with reference to the following Examples, but it should not be construed that the present invention is limited thereto.

【0021】実施例1〜10 クロメート処理をしないアルミニウム−亜鉛合金めっき
鋼板として、板厚が0.6mm、めっき層の組成がAl
=55%、Zn=43.4%、Si=1.6%(いずれ
も重量%)でめっき付着量が片面75g/m2 のものを
使用した。試験片の大きさは、ビード付ハット成形試験
用は、250mm×50mm、その他の試験用は、15
0mm×75mmを用いた。
Examples 1 to 10 As an aluminum-zinc alloy-plated steel sheet not subjected to a chromate treatment, the thickness is 0.6 mm, and the composition of the plating layer is Al.
= 55%, Zn = 43.4%, Si = 1.6% (all in weight%) and a plating adhesion amount of 75 g / m 2 on one side. The size of the test piece was 250 mm x 50 mm for the hat-shaped bead-forming test, and 15 mm for the other tests.
0 mm × 75 mm was used.

【0022】一方、樹脂組成物は、表1に示すガラス転
移温度を有するポリエステル系樹脂またはポリウレタン
系樹脂250gと6価クロムを全クロムに対し50%含
む酸化クロム2.5gとに水を加えて1kgとし、これ
を日本パーカーライジング社製パルクリーナで30秒浸
漬し、樹脂水溶液または樹脂水分散液を作成した。この
樹脂水溶液または樹脂水分散液を脱脂処理した上記アル
ミニウム−亜鉛合金めっき鋼板の表面にバーコータNo
5〜No20を使用して、乾燥被膜量が2g/m2 とな
るように塗布した。この後、直ちに500℃の熱風乾燥
炉に5秒間入れて、乾燥造膜させた。このときの板温は
70℃であった。これを冷却することによって試験板と
した。なお、膜厚は試験片の塗装前後の重量を測定して
2g/m2 であることを確認した。
On the other hand, the resin composition was prepared by adding water to 250 g of a polyester resin or polyurethane resin having a glass transition temperature shown in Table 1 and 2.5 g of chromium oxide containing 50% of hexavalent chromium with respect to all chromium. 1 kg, and immersed in a Parker Rising Co., Ltd. Pal cleaner for 30 seconds to prepare a resin aqueous solution or a resin aqueous dispersion. A bar coater No. is applied to the surface of the aluminum-zinc alloy-plated steel sheet obtained by degreasing the resin aqueous solution or the resin aqueous dispersion.
Using No. 5 to No. 20, coating was performed so that the dry coating amount was 2 g / m 2 . Thereafter, the film was immediately placed in a hot-air drying oven at 500 ° C. for 5 seconds to form a dry film. The plate temperature at this time was 70 ° C. This was cooled to obtain a test plate. In addition, it was confirmed that the film thickness was 2 g / m 2 by measuring the weight of the test piece before and after coating.

【0023】[0023]

【表1】 [Table 1]

【0024】得られた試験片について、加工性、耐食
性、耐アルカリ性、加工部の耐食性および耐アルカリ性
ならびに被膜の色調を試験した。その結果を、表2に示
す。
The test pieces obtained were tested for workability, corrosion resistance, alkali resistance, corrosion resistance and alkali resistance of the processed part, and color tone of the coating. Table 2 shows the results.

【0025】比較例1〜3 樹脂組成物として、表1に示すアクリル系樹脂(1)
(中央理化工業(株)製、商品名 ES−20)、アク
リルースチレン系樹脂(旭化成(株)製、商品名ポリト
ロンF−2000)およびアクリル系樹脂(2)(東洋
紡(株)製、商品名 タフチックFC−490)を用い
た。これらの樹脂のガラス転移温度を測定した結果は、
表1のとおりであった。これらの樹脂を用い、実施例1
〜10と同じ方法で同じ大きさの試験片を得て、同じ試
験をした。その結果を表2に示す。
Comparative Examples 1 to 3 As resin compositions, acrylic resins (1) shown in Table 1 were used.
(Manufactured by Chuo Rika Kogyo Co., Ltd., trade name ES-20), acryl-styrene resin (manufactured by Asahi Kasei Corporation, trade name: Polytron F-2000) and acrylic resin (2) (manufactured by Toyobo Co., Ltd., product Name Tuftic FC-490) was used. The results of measuring the glass transition temperature of these resins are:
As shown in Table 1. Example 1 using these resins
Specimens of the same size were obtained in the same manner as in Test Nos. 1 to 10 and subjected to the same test. Table 2 shows the results.

【0026】[0026]

【表2】 [Table 2]

【0027】次に、試験方法を説明する。この試験方法
は、以下の実施例、比較例でも同じく用いた。
Next, the test method will be described. This test method was similarly used in the following Examples and Comparative Examples.

【0028】(1)加工性 図1に示すビード付ハット成形試験機1を用いて、25
0mm×50mmの試験片11を、図1のように台3と
押え4の間に入れ、押え4を下降して試験片11を押え
た状態で、ポンチ2を70mm/secの速さで43m
m上昇させて試験片11に凸部を形成するとともに、台
3のビード部5によって試験片11を摺動させた。な
お、図2は加工後の試験機1および試験片11の断面図
を示し、図3は成形加工後の試験片11の斜視図であ
る。試験片の評価は、試験片の表面を目視観察して、次
の5点法で行う。
(1) Workability Using a hat-forming tester 1 with a bead shown in FIG.
A test piece 11 of 0 mm × 50 mm is inserted between the table 3 and the presser 4 as shown in FIG. 1 and the punch 2 is moved 43 m at a speed of 70 mm / sec with the presser 4 lowered and the test piece 11 pressed.
m, a convex portion was formed on the test piece 11, and the test piece 11 was slid by the bead portion 5 of the table 3. FIG. 2 is a sectional view of the test machine 1 and the test piece 11 after processing, and FIG. 3 is a perspective view of the test piece 11 after forming processing. Evaluation of the test piece is performed by the following five-point method by visually observing the surface of the test piece.

【0029】5 かじりや樹脂およびメタルにピックア
ップがない 4 かじりがわずかに生じ、樹脂およびメタルのピック
アップ5mg以下 3 かじりが若干生じ、樹脂およびメタルのピックアッ
プ5〜10mg 2 かじりがかなり生じ、樹脂およびメタルのピックア
ップ100mg 1 加工部が破断し、加工不能 (2)耐食性 5%食塩水による塩水噴霧試験 35℃×400時間
(JIS Z 2371) 試験片の目視による5段評価 5 白錆の発生なし 4 白錆発生率5%未満 3 白錆発生率5〜10% 2 白錆発生率10〜50% 1 白錆発生率50%以上 (3)耐アルカリ性 1%水酸化ナトリウム水溶液に浸漬試験 30℃×30
分 試験片の目視による5段階評価 5 黒錆の発生なし 4 黒錆がわずかに発生しているが、目立たない 3 黒錆が発生して、やや目立つ 2 黒錆が発生して、全体が黒くなっている 1 黒錆が発生して、非常に黒く被膜が一部脱落する (4)加工部耐食性 150mm×75mmの試験片を安田製作所製の曲げ試
験機によって、図4に示すD=10mm、R=5mmの
U字形試験片12を作り、曲げ面(図3の矢符13で示
す部分)の外側に5%食塩水を35℃で400時間噴霧
し、曲げ面を目視し、5段階評価する。
5 No galling or pick-up in resin and metal 4 Slight galling occurred, 5 mg or less of resin and metal pickup 3 Slight galling occurred, 5-10 mg of resin and metal pickup 2 Galling considerably occurred, resin and metal Pickup 100mg 1 Processed part is broken and processing is not possible (2) Corrosion resistance Salt spray test with 5% saline solution 35 ° C × 400 hours (JIS Z 2371) Five-step evaluation by visual inspection of test piece 5 No white rust 4 White Rust generation rate less than 5% 3 White rust generation rate 5-10% 2 White rust generation rate 10-50% 1 White rust generation rate 50% or more (3) Alkali resistance 1% sodium hydroxide aqueous solution immersion test 30 ° C × 30
Minute 5-stage evaluation of test specimen visually 5 No black rust 4 Slight black rust is generated but not noticeable 3 Black rust is generated and slightly noticeable 2 Black rust is generated and the whole is black 1 Black rust is generated and the coating is very black, and a part of the coating falls off. (4) Corrosion resistance of the processed part A 150 mm × 75 mm test piece was D = 10 mm shown in FIG. 4 by a bending tester manufactured by Yasuda Seisakusho. A U-shaped test piece 12 of R = 5 mm was prepared, and 5% saline solution was sprayed at 35 ° C. for 400 hours on the outside of the bent surface (portion indicated by an arrow 13 in FIG. 3). I do.

【0030】評点は、(2)の耐食性と同じ。The score is the same as the corrosion resistance of (2).

【0031】(5)加工部耐アルカリ性 (4)と同様の方法で、同様の試験片を作り、曲げ面を
0.5%水酸化ナトリウム水溶液に30℃で15分浸漬
し、曲げ面を目視で5段階評価する。
(5) Alkali Resistance in Processed Section A similar test piece was prepared in the same manner as in (4), and the bent surface was immersed in a 0.5% aqueous sodium hydroxide solution at 30 ° C. for 15 minutes, and the bent surface was visually observed. Is evaluated on a 5-point scale.

【0032】評点は、(3)の耐アルカリ性と同じ。The rating is the same as the alkali resistance of (3).

【0033】(6)被膜の色調 目視で下地の鋼板との色の差を観察し、5段階評価す
る。
(6) Color Tone of Coating The difference in color between the steel sheet and the base steel sheet is visually observed and evaluated in five levels.

【0034】5 下地の鋼板と同色 4 下地の鋼板とわずかに色が違う 3 やや黄色に見える 2 かなり黄色く見える 1 黄色く見える 実施例1〜10と比較例1〜3とから、ポリエステル系
およびポリウレタン系樹脂を用いるものが従来のアクリ
ル系樹脂を用いたものよりも非加工部および加工部の耐
アルカリ性に優れていることが判る。
5 Same color as the base steel plate 4 Slightly different color from the base steel plate 3 Appears slightly yellow 2 Appears quite yellow 1 Appears yellow From Examples 1-10 and Comparative Examples 1-3, polyester-based and polyurethane-based It can be seen that those using a resin are more excellent in alkali resistance of the non-processed portion and the processed portion than those using a conventional acrylic resin.

【0035】実施例11 樹脂組成物の樹脂分として、表1のポリエステル樹脂
(1)(ガラス転移温度が40℃以上)とポリエステル
樹脂(2)(ガラス転移温度が40℃未満)とを95:
5の割合で混合したものを用いた他は、実施例1〜10
と同じ方法で同じ大きさの試験片を得て同じ試験をし
た。その結果を、表3に示す。
Example 11 As the resin components of the resin composition, the polyester resin (1) (glass transition temperature of 40 ° C. or more) and polyester resin (2) (glass transition temperature of less than 40 ° C.) in Table 1 were 95:
Examples 1 to 10 were used except that a mixture of 5 was used.
A test piece of the same size was obtained in the same manner as in Example 1 and the same test was performed. Table 3 shows the results.

【0036】実施例12 樹脂組成物の樹脂分として、表1のポリエステル樹脂
(1)(ガラス転移温度が40℃以上)とポリエステル
樹脂(2)(ガラス転移温度が40℃未満)とを50:
50の割合で混合したものを用いた他は、実施例1〜1
0と同じ方法で同じ大きさの試験片を得て同じ試験をし
た。その結果を、表3に示す。
Example 12 As the resin component of the resin composition, the polyester resin (1) (having a glass transition temperature of 40 ° C. or more) and the polyester resin (2) (having a glass transition temperature of less than 40 ° C.) shown in Table 1 were 50:
Examples 1 to 1 were used except that a mixture of 50 and 50 was used.
A test piece of the same size was obtained in the same manner as in Example 0, and the same test was performed. Table 3 shows the results.

【0037】実施例13 樹脂組成物の樹脂分として、表1のポリエステル樹脂
(1)(ガラス転移温度が40℃以上)とポリエステル
樹脂(2)(ガラス転移温度が40℃未満)とを40:
60の割合で混合したものを用いた他は、実施例1〜1
0と同じ方法で同じ大きさの試験片を得て同じ試験をし
た。その結果を、表3に示す。
Example 13 As resin components of the resin composition, the polyester resin (1) (having a glass transition temperature of 40 ° C. or more) and the polyester resin (2) (having a glass transition temperature of less than 40 ° C.) shown in Table 1 were 40:
Examples 1 to 1 were used except that a mixture of 60 and 60 was used.
A test piece of the same size was obtained in the same manner as in Example 0, and the same test was performed. Table 3 shows the results.

【0038】実施例14 樹脂組成物の樹脂分として表1のポリエステル樹脂
(2)(ガラス転移温度40℃未満)と、ポリエステル
樹脂(3)(ガラス転移温度40℃以上)と、ポリウレ
タン樹脂(1)(ガラス転移温度40℃以上)とを3
0:40:30の割合で混合したものを用いた他は、実
施例1〜10と同じ方法で同じ大きさの試験片を得て同
じ試験をした。その結果を、表3に示す。
Example 14 As resin components of the resin composition, polyester resin (2) shown in Table 1 (glass transition temperature of less than 40 ° C.), polyester resin (3) (glass transition temperature of 40 ° C. or more), and polyurethane resin (1) ) (Glass transition temperature 40 ° C or higher) and 3
Except that a mixture of 0:40:30 was used, a test piece of the same size was obtained by the same method as in Examples 1 to 10, and the same test was performed. Table 3 shows the results.

【0039】[0039]

【表3】 [Table 3]

【0040】実施例1〜14の結果から、耐アルカリ性
は、ガラス転移温度が40℃未満の樹脂のみを使ったも
のおよびその割合が50%以上のもので若干劣ることが
判り、また加工部耐アルカリ性は、逆にガラス転移温度
が40℃以上の樹脂のみを使ったもので劣ることが判
る。しかし、ガラス転移温度が40℃以上の樹脂を95
〜50%と、ガラス転移温度が40℃未満の樹脂を5〜
50%混ぜることによって、非加工部および加工部の耐
アルカリ性が改善されることが判る。
From the results of Examples 1 to 14, it was found that the alkali resistance was slightly inferior to those using only a resin having a glass transition temperature of less than 40 ° C. and those having a ratio of 50% or more. On the contrary, it is understood that the alkalinity is inferior to those using only a resin having a glass transition temperature of 40 ° C. or higher. However, a resin having a glass transition temperature of 40 ° C.
5050%, and a resin having a glass transition temperature of less than 40 ° C.
It can be seen that mixing by 50% improves the alkali resistance of the non-processed portion and the processed portion.

【0041】実施例15〜17 樹脂組成物の樹脂分として、表1のポリエステル樹脂
(1)を用い、これに添加する酸化クロムを、全クロム
に対する6価クロムの割合が30%以上で表4のように
変えた他は、実施例1〜10と同じ方法で同じ大きさの
試験片を作って同じ試験をした。その結果を、実施例1
の結果とともに表4に示す。
Examples 15 to 17 The polyester resin (1) shown in Table 1 was used as the resin component of the resin composition, and the chromium oxide to be added was changed when the ratio of hexavalent chromium to all chromium was 30% or more. Except having changed as described above, test pieces of the same size were prepared in the same manner as in Examples 1 to 10, and the same test was performed. The results are shown in Example 1.
The results are shown in Table 4 together with the results.

【0042】比較例4 樹脂組成物の樹脂分として、表1のポリエステル樹脂
(1)を用い、これに添加する酸化クロムを、全クロム
に対する6価クロムの割合が30%未満(20%)にな
るようにした他は、実施例1〜10と同じ方法で同じ大
きさの試験片を作って同じ試験をした。その結果を、表
4に示す。
Comparative Example 4 The polyester resin (1) shown in Table 1 was used as the resin component of the resin composition, and the chromium oxide to be added was changed so that the ratio of hexavalent chromium to all chromium was less than 30% (20%). Other than that, test pieces of the same size were prepared in the same manner as in Examples 1 to 10, and the same test was performed. Table 4 shows the results.

【0043】[0043]

【表4】 [Table 4]

【0044】表4から、全クロムに対する6価クロムの
割合が30%未満では、非加工部および加工部の耐食性
が劣ることが判る。
From Table 4, it can be seen that when the ratio of hexavalent chromium to the total chromium is less than 30%, the corrosion resistance of the unprocessed portion and the processed portion is poor.

【0045】実施例18,19 樹脂組成物の樹脂として、表1のポリエステル樹脂
(1)を用い、これに添加する酸化クロム量を表5に示
す0.75〜12.5g(樹脂固形分比で0.3〜5
%)にした他は、実施例1〜10と同じ方法で同じ大き
さの試験片を作って同じ試験をした。その結果を、実施
例1の結果とともに表5に示す。また、酸化クロムを含
んだ樹脂組成物の安定性を調べるために、調整した樹脂
組成物を1週間放置したが、樹脂組成物には変化はなか
った。
Examples 18 and 19 The polyester resin (1) shown in Table 1 was used as the resin of the resin composition, and the amount of chromium oxide added to the resin was 0.75 to 12.5 g shown in Table 5 (resin solid content ratio). 0.3 to 5
%), The same test was performed by preparing test pieces of the same size in the same manner as in Examples 1 to 10. Table 5 shows the results together with the results of Example 1. Further, in order to examine the stability of the resin composition containing chromium oxide, the prepared resin composition was left for one week, but there was no change in the resin composition.

【0046】比較例5,6 樹脂組成物の樹脂として、表1のポリエステル樹脂
(1)を用い、これに添加する酸化クロム量を表5に示
す0.75gおよび12.5g(樹脂固形分比で0.3
%未満および5%を超える量)にした他は、実施例1〜
10と同じ方法で同じ大きさの試験片を作って同じ試験
をした。その結果を、表5に示す。また、実施例18,
19で行ったと同様に樹脂組成物の安定性を調べるため
に、調整した樹脂組成物を1週間放置した。その結果、
酸化クロムの添加量が少ない比較例5では、樹脂組成物
に変化はなかったが、酸化クロムの添加量が多い比較例
6では酸化クロムの沈澱が生じた。さらに、樹脂固形分
比で10%以上の酸化クロムを添加した樹脂組成物で
は、1週間後にゲル化し、使用不能となった。
Comparative Examples 5 and 6 The polyester resin (1) shown in Table 1 was used as the resin of the resin composition, and the amount of chromium oxide added to the resin was 0.75 g and 12.5 g shown in Table 5 (resin solid content ratio). 0.3
% And more than 5%).
Test pieces of the same size were prepared in the same manner as in Example 10 and subjected to the same test. Table 5 shows the results. In Example 18,
In order to examine the stability of the resin composition in the same manner as in Step 19, the prepared resin composition was left for one week. as a result,
In Comparative Example 5 in which the amount of chromium oxide added was small, there was no change in the resin composition, but in Comparative Example 6 in which the amount of chromium oxide was large, precipitation of chromium oxide occurred. Furthermore, the resin composition containing 10% or more of chromium oxide at a resin solid content ratio gelled after one week and became unusable.

【0047】[0047]

【表5】 [Table 5]

【0048】これから、酸化クロム添加量が0.3%未
満または5%を超える樹脂組成物は、非加工部耐食性が
劣り、また酸化クロム添加量が5%を超える過クロム樹
脂は非加工部および加工部の耐アルカリ性、加工部耐食
性が劣り、また被膜の色調も悪いことが判る。また、酸
化クロムの添加量が多いと時間経過とともに、沈澱を生
じる傾向があるが、5%以下では1週間後でも沈澱を生
ぜず、安定な樹脂組成物であることが判る。
From the above, it can be seen that the resin composition containing less than 0.3% or more than 5% of chromium oxide has inferior corrosion resistance in the non-processed portion, and the perchromic resin containing more than 5% of chromium oxide has no corrosion in the non-processed portion. It can be seen that the alkali resistance and the corrosion resistance of the processed part are inferior, and the color tone of the coating is also poor. When the amount of chromium oxide added is large, precipitation tends to occur with the passage of time, but when it is 5% or less, precipitation does not occur even after one week, indicating that the resin composition is stable.

【0049】実施例20,21 樹脂組成物の樹脂として、表1のポリエステル樹脂
(1)を用い、試験片に塗布する樹脂の膜厚を表6に示
す0.3〜4g/m2の厚さにした他は、実施例1〜1
0と同じ方法で同じ大きさの試験片を作って同じ試験を
した。その結果を、実施例1の結果とともに表6に示
す。
Examples 20 and 21 The polyester resin (1) shown in Table 1 was used as the resin of the resin composition, and the thickness of the resin applied to the test piece was 0.3 to 4 g / m 2 shown in Table 6. Other than the above, Examples 1-1
Specimens of the same size were prepared in the same manner as in Test No. 0 and subjected to the same test. Table 6 shows the results together with the results of Example 1.

【0050】比較例7,8 樹脂組成物の樹脂として、表1のポリエステル樹脂
(1)を用い、試験片に塗布する樹脂の膜厚を表6に示
す0.3g/m2未満(0.1g/m2)または4g/m
2を超える厚さ(5g/m2)にした他は、実施例1〜1
0と同じ方法で同じ大きさの試験片を作って同じ試験を
した。その結果を、表6に示す。
Comparative Examples 7 and 8 The polyester resin (1) shown in Table 1 was used as the resin of the resin composition, and the thickness of the resin applied to the test piece was less than 0.3 g / m 2 shown in Table 6 (0. 1 g / m 2 ) or 4 g / m
Examples 1 to 1 except that the thickness was more than 2 (5 g / m 2 )
Specimens of the same size were prepared in the same manner as in Test No. 0 and subjected to the same test. Table 6 shows the results.

【0051】[0051]

【表6】 [Table 6]

【0052】これから、膜厚が0.3g/m2未満のと
きは、非加工部および加工部耐食性ならびに非加工部お
よび加工部耐アルカリ性が劣り、膜厚が4g/m2を超
える厚さのときは、非加工部および加工部耐アルカリ性
が劣り、被膜色調が若干悪いことが判る。
From this, when the film thickness is less than 0.3 g / m 2 , the corrosion resistance of the non-processed portion and the processed portion and the alkali resistance of the non-processed portion and the processed portion are inferior, and when the film thickness exceeds 4 g / m 2. In some cases, it was found that the alkali resistance of the unprocessed portion and the processed portion was poor, and the color tone of the film was slightly poor.

【0053】実施例22,23 樹脂組成物の樹脂として、表1のポリエステル樹脂
(1)を用い、これにオレフィン系ワックス(三洋化成
工業(株)製、商品名 パーマリンRN)を表7で示す
樹脂固形分比で、0.1〜20%添加した他は、実施例
1〜10と同じ方法で同じ大きさの試験片を作って同じ
試験をした。その結果を、表7に示す。
Examples 22 and 23 The polyester resin (1) shown in Table 1 was used as the resin of the resin composition, and the olefin wax (trade name: Permarine RN, manufactured by Sanyo Chemical Industries, Ltd.) is shown in Table 7. Except that 0.1 to 20% was added at a resin solid content ratio, test pieces of the same size were prepared in the same manner as in Examples 1 to 10, and the same test was performed. Table 7 shows the results.

【0054】比較例9 樹脂組成物の樹脂として、表1のポリエステル樹脂
(1)を用い、これにオレフィン系ワックス(三洋化成
工業(株)製、商品名 パーマリンRN)を表7で示す
樹脂固形分比で、20%を超える量(25%)添加した
他は、実施例1〜10と同じ方法で、同じ大きさの試験
片を作って同じ試験をした。その結果を、オレフィンワ
ックスを加えない実施例1の結果とともに表7に示す。
Comparative Example 9 As a resin of the resin composition, a polyester resin (1) shown in Table 1 was used, and an olefin-based wax (trade name: Permarin RN, manufactured by Sanyo Chemical Industries, Ltd.) was used. A test piece of the same size was prepared and subjected to the same test in the same manner as in Examples 1 to 10, except that an amount of more than 20% (25%) was added in a fractional ratio. The results are shown in Table 7 together with the results of Example 1 in which no olefin wax was added.

【0055】[0055]

【表7】 [Table 7]

【0056】これから、ワックスの添加によって加工性
が若干向上するが、添加量が20%を超えると非加工部
および加工部耐アルカリ性が低下することが判る。
From this, it can be seen that the workability is slightly improved by the addition of the wax, but when the added amount exceeds 20%, the alkali resistance of the non-processed portion and the processed portion decreases.

【0057】実施例24〜26 試験片に表8に示す60mg/m2未満の厚さにクロメ
ート処理をしたアルミニウム−亜鉛合金めっき鋼板(ア
ルミニウム−亜鉛合金めっきの条件は、実施例1〜10
と同じ)に、樹脂組成物の樹脂として、表1のポリエス
テル樹脂(1)を用いて、実施例1〜10と同じ方法で
同じ大きさの試験片を作って同じ試験をした。その結果
を、クロメート処理をしない実施例1の結果とともに表
8に示す。
Examples 24-26 Aluminum-zinc alloy-coated steel sheets obtained by subjecting test pieces to a thickness of less than 60 mg / m 2 as shown in Table 8 (the conditions for aluminum-zinc alloy plating were as described in Examples 1-10).
The same test as in Examples 1 to 10 was performed using the polyester resin (1) shown in Table 1 as the resin of the resin composition. The results are shown in Table 8 together with the results of Example 1 without chromate treatment.

【0058】比較例10 試験片に表8に示す60mg/m2の厚さにクロメート
処理をしたアルミニウム−亜鉛合金めっき鋼板(アルミ
ニウム−亜鉛合金めっきの条件は、実施例1〜10と同
じ)に、樹脂組成物の樹脂として、表1のポリエステル
樹脂(1)を用いて、実施例1〜10と同じ方法で同じ
大きさの試験片を作って同じ試験をした。その結果を、
クロメート処理をしない実施例1の結果とともに表8に
示す。
Comparative Example 10 An aluminum-zinc alloy-plated steel sheet (the conditions for aluminum-zinc alloy plating were the same as in Examples 1 to 10) in which a test piece was chromate-treated to a thickness of 60 mg / m 2 shown in Table 8 was used. Using the polyester resin (1) shown in Table 1 as the resin of the resin composition, test pieces of the same size were prepared in the same manner as in Examples 1 to 10, and the same test was performed. The result is
Table 8 shows the results of Example 1 without chromate treatment.

【0059】[0059]

【表8】 [Table 8]

【0060】これから、クロメート処理の厚さが少ない
か、またはないと加工部の耐食性または耐アルカリ性が
若干悪くなることが判る。反対に、クロメート処理の厚
さが60mg/m2以上になると被膜の色調が悪くなる
ことが判る。
From this, it is understood that the corrosion resistance or alkali resistance of the processed portion is slightly deteriorated if the thickness of the chromate treatment is small or not. Conversely, when the thickness of the chromate treatment is 60 mg / m 2 or more, the color tone of the coating becomes poor.

【0061】[0061]

【発明の効果】以上のように、本発明によれば、クロム
酸化合物を配合したポリエステル系樹脂またはポリウレ
タン系樹脂で表面処理する1層処理で、加工性、耐アル
カリ性および耐食性に優れ、その色調も従来品と同等ま
たはそれ以上の表面処理アルミニウム−亜鉛合金めっき
鋼板が得られる。
As described above, according to the present invention, a one-layer treatment in which the surface is treated with a polyester resin or a polyurethane resin containing a chromic acid compound is excellent in workability, alkali resistance and corrosion resistance, and its color tone Also, a surface-treated aluminum-zinc alloy-plated steel sheet equal to or more than the conventional product can be obtained.

【図面の簡単な説明】[Brief description of the drawings]

【図1】試験片11の加工性を試験するためのビード付
ハット試験機1の断面図である。
FIG. 1 is a sectional view of a hat-equipped hat tester 1 for testing the workability of a test piece 11;

【図2】ビード付ハット試験機1で試験片11を加工し
た状態を示す断面図である。
FIG. 2 is a cross-sectional view showing a state where a test piece 11 has been processed by a hat tester 1 with a bead.

【図3】ビード付ハット試験機1で加工成形された試験
片11の斜視図である。
FIG. 3 is a perspective view of a test piece 11 processed and formed by the hat-equipped hat tester 1;

【図4】加工部耐食性および加工部耐アルカリ性を試験
する試験片12の断面図である。
FIG. 4 is a cross-sectional view of a test piece 12 for testing the corrosion resistance of the processed portion and the alkali resistance of the processed portion.

【符号の説明】[Explanation of symbols]

1 ビード付ハット試験機 11 加工性用試験片 12 加工部耐食性および加工部耐アルカリ性用試験片 DESCRIPTION OF SYMBOLS 1 Hat test machine with a bead 11 Test piece for workability 12 Test piece for corrosion resistance and alkali resistance in a processed part

───────────────────────────────────────────────────── フロントページの続き (72)発明者 保母 芳彦 和歌山県和歌山市湊1850番地 住友金属 工業株式会社 和歌山製鉄所内 (72)発明者 福留 博 和歌山県和歌山市湊1850番地 住友金属 工業株式会社 和歌山製鉄所内 (72)発明者 植田 尚孝 和歌山県和歌山市湊1850番地 住友金属 工業株式会社 和歌山製鉄所内 (56)参考文献 特開 平4−28878(JP,A) 特開 平5−65667(JP,A) ──────────────────────────────────────────────────の Continued on the front page (72) Inventor Yoshihiko Hobo 1850 Minato, Wakayama, Wakayama Sumitomo Metal Industries, Ltd.Wakayama Works (72) Inventor Hiroshi Fukudome, 1850 Minato, Wakayama, Wakayama Sumitomo Metal Industries In-house (72) Inventor Naotaka Ueda 1850 Minato, Wakayama-shi, Wakayama Prefecture Sumitomo Metal Industries, Ltd. Wakayama Works (56) References JP-A-4-28878 (JP, A) JP-A-5-65667 (JP, A)

Claims (3)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】水分散性もしくは水溶性ポリエステル樹脂
または水分散性もしくは水溶性ポリウレタン樹脂の1種
または2種以上の混合物を含む樹脂分と、 前期樹脂分に対し、6価クロムを30%以上含むクロム
化合物を、酸化クロム換算で0.1〜5%とを配合した
樹脂組成物を、 アルミニウム−亜鉛合金めっき鋼板の表面に0.3〜4
g/m2 の乾燥重量の厚さで塗布したことを特徴とする
有機表面処理剤で処理されたアルミニウム−亜鉛合金め
っき鋼板。
1. A resin component containing one or more of a water-dispersible or water-soluble polyester resin or a water-dispersible or water-soluble polyurethane resin, and 30% or more of hexavalent chromium based on the resin component. A chromium compound containing 0.1 to 5% in terms of chromium oxide is coated on the surface of an aluminum-zinc alloy-plated steel sheet with 0.3 to 4%.
An aluminum-zinc alloy-plated steel sheet treated with an organic surface treating agent, wherein the aluminum-zinc alloy sheet is applied at a dry weight of g / m 2 .
【請求項2】 前記樹脂組成物が、ガラス転移温度40
℃以上の樹脂とガラス転移温度40℃未満の樹脂とを、
そのクロム酸化合物を除いた乾燥重量比で95:5〜5
0:50の割合で含む混合物であることを特徴とする請
求項1に記載の有機表面処理剤で処理されたアルミニウ
ム−亜鉛合金めっき鋼板。
2. The method according to claim 1, wherein the resin composition has a glass transition temperature of 40.
C. or more and a resin having a glass transition temperature of less than 40 ° C.
95: 5-5 by dry weight ratio excluding the chromic acid compound
The aluminum-zinc alloy-plated steel sheet treated with the organic surface treating agent according to claim 1, wherein the mixture is a mixture containing 0:50.
【請求項3】 前記樹脂組成物が、さらにオレフィン系
ワックスを乾燥重量で0.1〜20%含むことを特徴と
する請求項1または請求項2に記載の有機表面処理剤で
処理されたアルミニウム−亜鉛合金めっき鋼板。
3. The aluminum treated with an organic surface treating agent according to claim 1, wherein the resin composition further contains 0.1 to 20% by dry weight of an olefin-based wax. -Zinc alloy plated steel sheets.
JP4300107A 1992-11-10 1992-11-10 Aluminum-zinc alloy coated steel sheet treated with organic surface treatment agent Expired - Fee Related JP2721292B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP4300107A JP2721292B2 (en) 1992-11-10 1992-11-10 Aluminum-zinc alloy coated steel sheet treated with organic surface treatment agent

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP4300107A JP2721292B2 (en) 1992-11-10 1992-11-10 Aluminum-zinc alloy coated steel sheet treated with organic surface treatment agent

Publications (2)

Publication Number Publication Date
JPH06146001A JPH06146001A (en) 1994-05-27
JP2721292B2 true JP2721292B2 (en) 1998-03-04

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Country Link
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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU2004259971A1 (en) 2003-07-29 2005-02-03 Jfe Steel Corporation Surface-treated steel sheet and method for producing same
JP5433950B2 (en) 2008-01-24 2014-03-05 日本軽金属株式会社 Metal paint
JP5544782B2 (en) * 2009-08-07 2014-07-09 新日鐵住金株式会社 Paint composition for painted metal

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0428878A (en) * 1990-05-25 1992-01-31 Nisshin Steel Co Ltd Production of surface treated steel sheet excellent in corrosion resistance and chromium elution resistance
JP2617838B2 (en) * 1991-09-09 1997-06-04 新日本製鐵株式会社 Manufacturing method of high performance lubricated steel sheet

Also Published As

Publication number Publication date
JPH06146001A (en) 1994-05-27

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