JPS62225341A - Coated steel plate for bonding - Google Patents
Coated steel plate for bondingInfo
- Publication number
- JPS62225341A JPS62225341A JP6985286A JP6985286A JPS62225341A JP S62225341 A JPS62225341 A JP S62225341A JP 6985286 A JP6985286 A JP 6985286A JP 6985286 A JP6985286 A JP 6985286A JP S62225341 A JPS62225341 A JP S62225341A
- Authority
- JP
- Japan
- Prior art keywords
- paint
- adhesive
- plating
- epoxy
- steel plate
- 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
Links
- 229910000831 Steel Inorganic materials 0.000 title claims description 26
- 239000010959 steel Substances 0.000 title claims description 26
- 239000003973 paint Substances 0.000 claims description 52
- 230000001070 adhesive effect Effects 0.000 claims description 28
- 239000000853 adhesive Substances 0.000 claims description 27
- 238000007747 plating Methods 0.000 claims description 23
- 239000004593 Epoxy Substances 0.000 claims description 13
- 239000003822 epoxy resin Substances 0.000 claims description 12
- 229920000647 polyepoxide Polymers 0.000 claims description 12
- 229920000728 polyester Polymers 0.000 claims description 10
- 229920005989 resin Polymers 0.000 claims description 9
- 239000011347 resin Substances 0.000 claims description 9
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 claims description 8
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 7
- LRXTYHSAJDENHV-UHFFFAOYSA-H zinc phosphate Chemical compound [Zn+2].[Zn+2].[Zn+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O LRXTYHSAJDENHV-UHFFFAOYSA-H 0.000 claims description 7
- 229910000165 zinc phosphate Inorganic materials 0.000 claims description 7
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 claims description 6
- ZCDOYSPFYFSLEW-UHFFFAOYSA-N chromate(2-) Chemical compound [O-][Cr]([O-])(=O)=O ZCDOYSPFYFSLEW-UHFFFAOYSA-N 0.000 claims description 6
- 229910052804 chromium Inorganic materials 0.000 claims description 6
- 239000011651 chromium Substances 0.000 claims description 6
- 239000000463 material Substances 0.000 description 12
- 239000011248 coating agent Substances 0.000 description 9
- 238000000576 coating method Methods 0.000 description 9
- 238000010438 heat treatment Methods 0.000 description 5
- 239000010410 layer Substances 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- 239000000049 pigment Substances 0.000 description 5
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 4
- 239000011324 bead Substances 0.000 description 4
- 239000011521 glass Substances 0.000 description 4
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- SVONRAPFKPVNKG-UHFFFAOYSA-N 2-ethoxyethyl acetate Chemical compound CCOCCOC(C)=O SVONRAPFKPVNKG-UHFFFAOYSA-N 0.000 description 3
- 239000012298 atmosphere Substances 0.000 description 3
- 230000007423 decrease Effects 0.000 description 3
- 230000008021 deposition Effects 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 229910001335 Galvanized steel Inorganic materials 0.000 description 2
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 2
- 229910000611 Zinc aluminium Inorganic materials 0.000 description 2
- HXFVOUUOTHJFPX-UHFFFAOYSA-N alumane;zinc Chemical compound [AlH3].[Zn] HXFVOUUOTHJFPX-UHFFFAOYSA-N 0.000 description 2
- 238000005452 bending Methods 0.000 description 2
- 230000007797 corrosion Effects 0.000 description 2
- 238000005260 corrosion Methods 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 239000008397 galvanized steel Substances 0.000 description 2
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 239000012046 mixed solvent Substances 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 238000010422 painting Methods 0.000 description 2
- 239000013034 phenoxy resin Substances 0.000 description 2
- 229920006287 phenoxy resin Polymers 0.000 description 2
- 239000011701 zinc Substances 0.000 description 2
- 229910052725 zinc Inorganic materials 0.000 description 2
- 239000004925 Acrylic resin Substances 0.000 description 1
- 229920000178 Acrylic resin Polymers 0.000 description 1
- 229910018137 Al-Zn Inorganic materials 0.000 description 1
- 229910018573 Al—Zn Inorganic materials 0.000 description 1
- 241000447394 Desmos Species 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical group C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- YNPNZTXNASCQKK-UHFFFAOYSA-N Phenanthrene Natural products C1=CC=C2C3=CC=CC=C3C=CC2=C1 YNPNZTXNASCQKK-UHFFFAOYSA-N 0.000 description 1
- DGEZNRSVGBDHLK-UHFFFAOYSA-N [1,10]phenanthroline Chemical compound C1=CN=C2C3=NC=CC=C3C=CC2=C1 DGEZNRSVGBDHLK-UHFFFAOYSA-N 0.000 description 1
- 238000004026 adhesive bonding Methods 0.000 description 1
- 239000012790 adhesive layer Substances 0.000 description 1
- 239000004844 aliphatic epoxy resin Substances 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- UTDPRMMIFFJALK-UHFFFAOYSA-N bis(oxiran-2-ylmethyl) cyclohexane-1,1-dicarboxylate Chemical compound C1CCCCC1(C(=O)OCC1OC1)C(=O)OCC1CO1 UTDPRMMIFFJALK-UHFFFAOYSA-N 0.000 description 1
- 239000004841 bisphenol A epoxy resin Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 239000003431 cross linking reagent Substances 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 1
- 238000005498 polishing Methods 0.000 description 1
- 229920001225 polyester resin Polymers 0.000 description 1
- 239000004645 polyester resin Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- -1 surface treatment Substances 0.000 description 1
- 238000004381 surface treatment Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 238000003466 welding Methods 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Landscapes
- Laminated Bodies (AREA)
- Chemical Treatment Of Metals (AREA)
Abstract
(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.
Description
【発明の詳細な説明】
(産業上の利用分野)
本発明は、組立時に接着剤を使用する場合にその接着耐
久性に優れた塗装鋼板に関するものである。DETAILED DESCRIPTION OF THE INVENTION (Field of Industrial Application) The present invention relates to a coated steel plate that has excellent adhesive durability when an adhesive is used during assembly.
(従来の技術)
塗装鋼板を組立てるに際して溶接やかしめ等に用いた場
合には当該溶接部やかしめ部において塗装被膜が破壊さ
れて、塗装鋼板を使用するメリットが半減する為、近年
では塗装鋼板の組立てに際して金属接着剤が使用される
ようになってきた。(Prior art) When painted steel sheets are used for welding or caulking during assembly, the paint film is destroyed at the welded or caulked parts, reducing the benefit of using painted steel sheets by half. Metal adhesives have come to be used during assembly.
ところで、前記したような接着接合では塗装鋼板の各々
の層や面での接着強度が維持されなければならないこと
は勿論である。しかして、かかる場合の各層や面を具体
的に挙げると以下の如くである。By the way, in the above-mentioned adhesive bonding, it goes without saying that the adhesive strength of each layer or surface of the painted steel plate must be maintained. Specifically, the layers and surfaces in such a case are as follows.
■ 接着剤層
■ 接着剤/塗膜界面
■ 塗膜層
■ 塗膜/メッキ界面
■ メッキ層
■ メンキ/母材界面
(発明が解決しようとする問題点)
しかして、本発明者等が研究、実験を行なった結果によ
れば接着接合した場合には前記した各層や面のうち、■
、■、■に掲げた夫々の界面に問題が生じ易いことが判
明した。■ Adhesive layer ■ Adhesive/paint interface ■ Paint layer ■ Paint film/plating interface ■ Plating layer ■ Coating/base material interface (problem to be solved by the invention) Therefore, the present inventors conducted research, According to the results of experiments, when adhesively bonded, among the layers and surfaces described above,
It has been found that problems are likely to occur at each of the interfaces listed in , ■, and ■.
以下夫々について分脱する。We will discuss each of them below.
(A)接着剤/塗膜界面について
接着剤を塗布して貼合わせた後の加熱条件によっては再
塗装鋼板は十分に接着せず、接着剤/塗膜界面において
剥離が生じ易い。この傾向は特にポリエステル系やアク
リル系の塗料において著しい。(A) Adhesive/paint interface Depending on the heating conditions after applying the adhesive and bonding, the repainted steel plate may not adhere sufficiently, and peeling may easily occur at the adhesive/paint interface. This tendency is particularly remarkable in polyester-based and acrylic-based paints.
この剥離を防止するためには前記加熱条件を十分に採る
必要があるが、この加熱条件を十分に採る方法として、
■加熱時間を長くする、■加熱温度を上昇させる、とい
う方法がある。In order to prevent this peeling, it is necessary to sufficiently set the above-mentioned heating conditions, but as a method to sufficiently set these heating conditions,
There are two methods: ■ lengthen the heating time, and ■ raise the heating temperature.
しかし、■の方法は生産上、設備上の制約があり実用的
ではない。また■の方法は設備上の制約の他に塗料の樹
脂が劣化するという問題がある。However, method (2) is not practical due to production and equipment constraints. In addition, the method (2) has the problem of deterioration of the resin in the paint, in addition to equipment limitations.
すなわち、これらの方法はいずれも問題があり実際的で
はない。That is, all of these methods have problems and are not practical.
一方、エポキシ系やウレタン系の塗料は前記ポリエステ
ル系やアクリル系塗料のような問題は少なく、接着安定
性に優れているのであるが、塗装鋼板が曲げ加工等を施
されて使用される場合や耐候性を要求される場合等には
適さず使用可能な対象が限定される。On the other hand, epoxy-based and urethane-based paints do not have the same problems as the polyester-based and acrylic-based paints and have excellent adhesion stability. It is not suitable for cases where weather resistance is required, and the objects for which it can be used are limited.
(B)2膜/メッキ界面について
二枚の塗装鋼板を接着剤によって貼合せ、その後湿潤状
態に保持すると、経時と共にT型剥離強度が低下する。(B) Regarding the two-film/plating interface, when two coated steel plates are bonded together with an adhesive and then kept in a wet state, the T-peel strength decreases over time.
しかして、この剥離状況を観察すると、接着サンプルの
端部では塗膜/メッキ界面において剥離を生じており、
中央部では接着剤の凝集破壊を生じていた。そして、前
記端部での界面剥離は時間の経過と共に幅が広くなって
きた。However, when observing this peeling situation, it was found that peeling occurred at the coating/plating interface at the edge of the adhesive sample.
Cohesive failure of the adhesive occurred in the center. Then, the width of the interfacial peeling at the end portion became wider with the passage of time.
(C)メッキ/母材界面について
前記CB)において、塗膜/メッキ界面における剥離に
ついて説明したが、湿潤雰囲気下の保持時間が更に長く
なると、メッキ/母材界面において剥離が生じる場合が
ある。かかる場合におけるT型剥離強度は非常に小さい
ものとなる。(C) Regarding the plating/base material interface In CB) above, peeling at the coating film/plating interface was explained, but if the holding time in a humid atmosphere becomes longer, peeling may occur at the plating/base material interface. In such a case, the T-peel strength will be very small.
例えば、電気亜鉛メッキ鋼板を母材とすると、前記した
ようなメッキ/母材界面における剥離は生じ難いが、反
面、経済的な目付量である20〜40g/rrf(夫々
片面につき)では、溶融メッキ系の目付ff160 g
lrd以上の場合と比較して耐食性が劣る。For example, when an electrogalvanized steel sheet is used as the base material, peeling at the plating/base material interface as described above is unlikely to occur. Plated basis weight FF160 g
Corrosion resistance is inferior to that of lrd or higher.
従って、耐食性に優れた亜鉛系溶融メッキ鋼板を母材と
して使用する場合にはメッキ/母材界面における剥離を
抑制する必要がある。Therefore, when a zinc-based hot-dip plated steel sheet with excellent corrosion resistance is used as a base material, it is necessary to suppress peeling at the plating/base material interface.
本発明は上記した(A)〜(C)の3点を満足する、す
なわち接着耐久性に優れた塗装鋼板を提供せんとするも
のである。The present invention aims to provide a coated steel plate that satisfies the above three points (A) to (C), that is, has excellent adhesive durability.
(問題点を解決するための手段)
本発明は、1.5g/%以下の燐酸亜鉛処理あるいはク
ロム付着量が20〜150■/イのクロメート処理の少
なくともどちらか一方を下地処理して成るメッキ中のp
b含有量0.05重量%以下の亜鉛メッキ鋼板あるいは
亜鉛−アルミニウム系メッキ鋼板の接着剤の塗布される
面に、エポキシ系塗料、ウレタン系塗料、あるいはエポ
キシ樹脂を塗料中の樹脂に対して5〜20重量%を含む
ポリエステル系塗料又はアクリル系塗料のいずれか一つ
を塗布して成ることを要旨とする接着用塗装鋼板である
。(Means for Solving the Problems) The present invention provides plating that is formed by performing at least one of a zinc phosphate treatment with a coating weight of 1.5 g/% or less or a chromate treatment with a chromium adhesion amount of 20 to 150 cm/a as a base treatment. middle p
Apply epoxy paint, urethane paint, or epoxy resin to the adhesive-applied surface of a galvanized steel sheet or zinc-aluminum plated steel sheet with a b content of 0.05% by weight or less, based on the resin in the paint. This is a coated steel plate for adhesion, which is coated with either a polyester paint or an acrylic paint containing ~20% by weight.
本発明において、母材や下地処理、および塗料に前記し
たものを使用するのは前述した各界面における問題点を
解決するためであり、以下にその理由を説明する。In the present invention, the above-described materials are used for the base material, surface treatment, and paint in order to solve the problems at each interface described above, and the reason for this will be explained below.
(A)接着剤/塗膜界面について
塗膜に折曲げ性や耐候性等が要求されない場合には、エ
ポキシ系又はウレタン系の塗料を使用する。(A) Adhesive/paint interface If the paint film is not required to have bendability or weather resistance, an epoxy or urethane paint is used.
そして、折曲げ性や耐候性等が要求される場合には、ポ
リエステル系又はアクリル系塗料の樹脂に対して5〜2
0ft1%のエポキシ樹脂を添加した塗料を使用する。If bending properties, weather resistance, etc. are required, 5 to 2
Use a paint containing 0ft1% epoxy resin.
この場合、エポキシ樹脂の添加量が5重世%未満では下
記第1表に示すように接着の安定性確保が不足し、また
、20重量%を超えた場合には同じく下記第1表に示す
ようにエポキシの剛直性が現われ塗膜の加工性を損うか
ら、エポキシ樹脂の添加量は5〜20重景%とするので
ある。In this case, if the amount of epoxy resin added is less than 5% by weight, the stability of adhesion is insufficient as shown in Table 1 below, and if it exceeds 20% by weight, it is also shown in Table 1 below. Since the rigidity of epoxy appears and impairs the workability of the coating film, the amount of epoxy resin added is set at 5 to 20%.
なお、エポキシ樹脂に関しては塗料と相溶するものであ
れば特に種類は問わない。しかし、塗膜に耐候性が要求
される場合には芳香族を含むエポキシ樹脂、例えばビス
フェノールA型エポキシ樹脂より、脂肪族系のエポキシ
樹脂、例えばジグリシジルシクロヘキサンジカルボキシ
レート系エポキシ樹脂等を使用することが好ましい。The type of epoxy resin is not particularly limited as long as it is compatible with the paint. However, when weather resistance is required for the coating film, aliphatic epoxy resins such as diglycidyl cyclohexanedicarboxylate epoxy resins are used rather than aromatic epoxy resins such as bisphenol A epoxy resins. It is preferable.
(B)塗膜/メッキ界面について 塗装の下地処理としてクロメート処理を行なう。(B) About the coating film/plating interface Chromate treatment is performed as a base treatment for painting.
この場合、クロム付着量としては20〜150■/dの
範囲であることが必要であ。すなわち、20n+g/r
rf未満では侵入する水に対して抵抗力が弱く、従って
メッキに腐食が生じて接着力が減少するからである。他
方、150■/dを超えると下記第2表に示すように塗
装鋼板の折曲げ性劣化やT型剥離強度の低下が生じるか
らである。In this case, the amount of chromium deposited must be in the range of 20 to 150 .mu./d. That is, 20n+g/r
This is because if it is less than RF, the resistance against invading water is weak, and therefore the plating will corrode and the adhesive strength will decrease. On the other hand, if it exceeds 150 .mu./d, the bendability of the coated steel sheet deteriorates and the T-peel strength decreases, as shown in Table 2 below.
なお、燐酸亜鉛処理あるいは燐酸亜鉛処理後、前記した
クロメート処理を施しても同様の結果が得られる。この
場合の燐酸亜鉛処理は1.5g/rrr以下であること
が必要であることを本発明者等は実験によって確認して
いる。Note that similar results can be obtained even if the zinc phosphate treatment or the above-mentioned chromate treatment is performed after the zinc phosphate treatment. The present inventors have confirmed through experiments that the zinc phosphate treatment in this case needs to be 1.5 g/rrr or less.
第2表 クロメート付着量の影響
(C)メッキ/母材界面について
5%八へ−Zn−ミツシュメタルのメッキ鋼ヰ反である
ガルファン(商標名)、55%Al−Znのメッキ鋼板
であるガルバリウム(商標名)を用いると湿潤雰囲気下
でのメッキ剥離は生じない。Table 2 Effect of chromate deposition amount (C) Plating/base material interface 5% to 8-Zn-Mitshu metal plated steel Galfan (trade name), 55% Al-Zn plated steel plate Galvalume (trade name) (trade name), the plating will not peel off in a humid atmosphere.
また、一般の溶融亜鉛メッキ鋼板ではメッキ中のpb含
有量を0.05重貴簡以下にすることによってメッキ剥
離を防止できる。このことは下記第3表より明らかであ
る。Further, in the case of a general hot-dip galvanized steel sheet, peeling of the plating can be prevented by controlling the PB content in the plating to 0.05 or less. This is clear from Table 3 below.
第3表 湿潤雰囲気下でのメッキ颯聴性、接着強度変化
(作 用)
本発明に係る接着用塗装鋼板は、1.5g/d以下の燐
酸亜鉛処理あるいはクロム付着量が20〜150■/d
のクロメート処理の少なくともどちらか一方を下地処理
して成るメッキ中のpb含有to、os重量%以下の亜
鉛メッキ鋼板あるいは亜鉛−アルミニウム系メッキ鋼板
の接着剤の塗布される面に、エポキシ系塗料、ウレタン
系塗料、あるいはエポキシ樹脂を塗料中の樹脂に対して
5〜20重量%を含むポリエステル系塗料又はアクリル
系塗料のいずれか一つを塗布して成る構成である為、メ
ッキ/母材界面、塗膜/メッキ界面及び接着剤/塗膜界
面での剥離を防止できる。Table 3: Plating audibility and adhesive strength change in a humid atmosphere (effects) The coated steel sheet for adhesion according to the present invention is treated with zinc phosphate of 1.5 g/d or less or has a chromium deposit of 20 to 150 μ/d.
Epoxy paint, Since it is constructed by applying either a urethane paint or a polyester paint or an acrylic paint containing 5 to 20% by weight of epoxy resin based on the resin in the paint, the plating/base material interface, Peeling at the paint film/plating interface and adhesive/paint film interface can be prevented.
(実 施 例)
厚さ0.5鶴の亜鉛系溶融メッキ14板をスコッチブラ
イト(住友3M製、商品名)により研磨して表面を清浄
にした後、ボンデライト1415A(日本バーカーライ
ジング製、商品名)を塗布し乾燥した。その後、下記に
示す各塗料を乾燥膜厚10μとなるよう塗布し、鋼板温
度が210〜220℃になるよう焼付けた。各塗料の調
整は以下に示す如くである。(Example) After cleaning the surface by polishing 14 zinc-based hot-dip plated plates with a thickness of 0.5 mm using Scotch Brite (manufactured by Sumitomo 3M, trade name), Bonderite 1415A (manufactured by Nippon Barker Rising, trade name) was polished. ) was applied and dried. Thereafter, each of the paints shown below was coated to a dry film thickness of 10 μm, and the steel plate was baked to a temperature of 210 to 220°C. The adjustment of each paint is as shown below.
1)エポキシ系塗料
Union Carbide Co、製Bakelit
eフェノキシ樹脂PK[lを用いた。PKH)120部
に対し酢酸セロソルブ/キシレン=67/33 (重量
比)の混合溶媒80部を用いて溶解した。そして、この
樹脂溶液100部に対し、酸化チタン顔料(石層産業製
タイベークR−820)16部を加え、ガラスピーズに
より顔料を分散させた。1) Epoxy paint Bakerit manufactured by Union Carbide Co.
e Phenoxy resin PK[l was used. PKH) was dissolved in 80 parts of a mixed solvent of cellosolve acetate/xylene=67/33 (weight ratio). Then, 16 parts of a titanium oxide pigment (Tiebake R-820 manufactured by Ishiya Sangyo Co., Ltd.) was added to 100 parts of this resin solution, and the pigment was dispersed using glass beads.
2)ウレタン塗料
Bayer AG製Desmodur L、Desmo
phen 2001を用いた。Desmophen 2
001 100部をメチルエチルケトン150部に溶解
し、前記の酸化チタン100部を加え、ガラスピーズに
より顔料を分散させた。2) Urethane paint Desmodur L, Desmo manufactured by Bayer AG
phen 2001 was used. Desmophen 2
001 was dissolved in 150 parts of methyl ethyl ketone, 100 parts of the titanium oxide described above was added, and the pigment was dispersed using glass beads.
そして塗装の直前に、この樹脂溶液350部にDesm
odur L 25部を添加、攪拌して用いた。Immediately before painting, add 350 parts of this resin solution to Desm.
25 parts of odur L was added, stirred, and used.
3)ポリエステル塗料
東洋紡製バイロン103を用いた。バイロン10302
0部に対し、酢酸セロソルブ/キシレン−67/33(
重量比)の混合溶媒80部を用いて溶解した。そして、
架橋剤としてメチロール化メラミン(大日本インキ化学
製スーパーベフカミンJ 820)を4部加えた。また
、前記の酸化チタン顔料16部を樹脂溶液に加えてガラ
スピーズにより分散させた。3) Polyester paint Byron 103 manufactured by Toyobo was used. Byron 10302
For 0 parts, cellosolve acetate/xylene-67/33 (
The mixture was dissolved using 80 parts of a mixed solvent (weight ratio). and,
Four parts of methylolated melamine (Superbefkamine J 820, manufactured by Dainippon Ink Chemical) was added as a crosslinking agent. Further, 16 parts of the titanium oxide pigment described above was added to the resin solution and dispersed using glass beads.
添加するエポキシ樹脂は油化シェルエポキシ製エピコー
ト1004を用い、これをポリエステル樹脂溶解時に添
加した。The epoxy resin to be added was Epicoat 1004 manufactured by Yuka Shell Epoxy, and this was added when the polyester resin was dissolved.
なお、ポリエステル塗料の適用には、前述のフェノキシ
樹脂系エポキシ塗料をプライマーとして用いた。そして
、エポキシ塗料を乾燥i厚5μになるよう塗布し焼付け
た後、ポリエステル塗料を塗布した。In addition, when applying the polyester paint, the aforementioned phenoxy resin-based epoxy paint was used as a primer. Then, after applying epoxy paint to a dry thickness of 5 μm and baking, polyester paint was applied.
4)アクリル塗料
Rohn and Haas Co、製Acryloi
d AT−56を用いた。Acryloid AT
−5620部、スーパーベッカミンJ820 3部を酢
酸セロソルブ80部に溶解した。前記の酸化チタン顔料
16部を樹脂溶液に加え、ガラスピーズにて分散させた
。4) Acrylic paint Acryloi manufactured by Rohn and Haas Co.
d AT-56 was used. Acryloid AT
-5620 parts and 3 parts of Super Beckamine J820 were dissolved in 80 parts of cellosolve acetate. 16 parts of the titanium oxide pigment described above was added to the resin solution and dispersed using glass beads.
添加するエポキシ樹脂は油化シェル エポキシ製エピコ
ート1004を用い、これをアクリル樹脂溶解時に添加
した。The epoxy resin to be added was Epicoat 1004 manufactured by Yuka Shell Epoxy, and this was added when the acrylic resin was dissolved.
なお、ポリエステル塗料の場合と同様にエポキシ塗料を
プライマーとして用いた。Note that, as in the case of polyester paint, epoxy paint was used as a primer.
前述の塗装をした鋼板を200tlX25mmに切断し
た後、電気化学■製つレタン系接着剤ハードロフクを用
いて接着した。この時、塗膜面に接着剤を厚さ100μ
になるように塗布し、2枚の鋼板を貼合せ、150℃の
乾燥器に5分間保持した。The coated steel plate described above was cut into pieces of 200 tl x 25 mm and then glued together using a urethane adhesive Hardofuku made by Denki Kagaku (I). At this time, apply adhesive to the coating surface to a thickness of 100 μm.
Two steel plates were bonded together and kept in a dryer at 150°C for 5 minutes.
なお、試験片よりはみ出した接着剤はカッターナイフに
より除去した。Note that the adhesive that protruded from the test piece was removed using a cutter knife.
そして、貼合せた試験片を温度60℃、相対湿度90%
の雰囲気に保持し、接着強度の経時変化を測定した。Then, the bonded test piece was placed at a temperature of 60°C and a relative humidity of 90%.
The adhesive strength was measured over time.
この結果は前記第1表に示す如くである。なお、接着強
度はJIS K−6854に基づき、T型剥離試験に
より測定した。また剥離強度は繰返し5回の平均をとっ
た。また折曲げ性は塗装板の180部曲げを行ない、塗
膜にき裂が入らない板のはさみ枚数で評価した。The results are shown in Table 1 above. Note that the adhesive strength was measured by a T-peel test based on JIS K-6854. Moreover, the peel strength was averaged over 5 repetitions. The bendability was evaluated by bending 180 parts of the coated plate and determining the number of plates that could be bent without causing any cracks in the coating film.
(発明の効果)
以上説明したように本発明に係る接着用塗装鋼板は、1
.5g/nf以下の燐酸亜鉛処理あるいはクロム付着量
が20〜150■/dのクロメート処理の少なくともど
ちらか一方を下地処理して成るメッキ中のpb含有量0
.05重量%以下の亜鉛メッキ鋼板あるいは亜鉛−アル
ミニウム系メッキ鋼板の接着剤の塗布される面に、エポ
キシ系塗料、ウレタン系塗料、あるいはエポキシ樹脂を
塗料中の樹脂に対して5〜20重量%を含むポリエステ
ル系塗料又はアクリル系塗料のいずれか一つを塗布して
成る構成である為、メッキ/母材界面、塗膜/メッキ界
面及び接着剤/塗膜界面での剥離を防止でき、接着耐久
性に優れた接着用塗装鋼板が得られる。(Effects of the Invention) As explained above, the coated steel plate for adhesive according to the present invention has 1
.. Pb content 0 in plating formed by base treatment of at least one of zinc phosphate treatment with a chromium deposition amount of 5 g/nf or less or chromate treatment with a chromium deposition amount of 20 to 150 μ/d.
.. Apply epoxy paint, urethane paint, or epoxy resin at a concentration of 5 to 20% by weight based on the resin in the paint on the surface of the zinc-plated steel sheet or zinc-aluminum plated steel sheet where the adhesive is applied. Since the composition is coated with either polyester paint or acrylic paint, it is possible to prevent peeling at the plating/base material interface, paint film/plating interface, and adhesive/paint film interface, and the adhesive is durable. A coated steel plate for adhesion with excellent adhesive properties can be obtained.
Claims (1)
ロム付着量が20〜150mg/m^2のクロメート処
理の少なくともどちらか一方を下地処理して成るメッキ
中のPb含有量0.05重量%以下の亜鉛メッキ鋼板あ
るいは亜鉛−アルミニウム系メッキ鋼板の接着剤の塗布
される面に、エポキシ系塗料、ウレタン系塗料、あるい
はエポキシ樹脂を塗料中の樹脂に対して5〜20重量%
を含むポリエステル系塗料又はアクリル系塗料のいずれ
か一つを塗布して成ることを特徴とする接着用塗装鋼板
。(1) Pb content of 0.05 in plating formed by base treatment of at least one of zinc phosphate treatment with a 1.5 g/m^2 or less or chromate treatment with a chromium adhesion amount of 20 to 150 mg/m^2 Apply 5 to 20% by weight of epoxy paint, urethane paint, or epoxy resin to the surface of the zinc-plated steel sheet or zinc-aluminum-plated steel sheet to which the adhesive is applied, based on the resin in the paint.
A coated steel plate for adhesive use, characterized in that it is coated with either a polyester paint or an acrylic paint containing.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP6985286A JPS62225341A (en) | 1986-03-27 | 1986-03-27 | Coated steel plate for bonding |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP6985286A JPS62225341A (en) | 1986-03-27 | 1986-03-27 | Coated steel plate for bonding |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS62225341A true JPS62225341A (en) | 1987-10-03 |
Family
ID=13414753
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP6985286A Pending JPS62225341A (en) | 1986-03-27 | 1986-03-27 | Coated steel plate for bonding |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS62225341A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4959277A (en) * | 1988-12-07 | 1990-09-25 | Nihon Parkerizing Co., Ltd. | Process for treating plated steel sheet |
US5968662A (en) * | 1995-03-08 | 1999-10-19 | Nisshin Steel Co., Ltd. | Coated metal sheet bondable with adhesive |
JP2005271519A (en) * | 2004-03-26 | 2005-10-06 | Matsushita Electric Ind Co Ltd | Surface-treated steel plate and cooking device using it |
Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5342150A (en) * | 1976-09-30 | 1978-04-17 | Kawatetsu Galvanizing | Zinced steel sheet applied with primer coating which is spottweldable |
JPS5461277A (en) * | 1977-10-25 | 1979-05-17 | Kawatetsu Kohan Kk | Anticorrosive coated steel plate with good pressing processability |
JPS54112731A (en) * | 1978-02-24 | 1979-09-03 | Toyo Kohan Co Ltd | Composite covered steel plate |
JPS598354A (en) * | 1982-07-06 | 1984-01-17 | Matsushita Electronics Corp | Formation of metal film wiring |
JPS59171645A (en) * | 1983-03-19 | 1984-09-28 | 日新製鋼株式会社 | Weldable coated steel plate having excellent corrosion protection |
JPS6050181A (en) * | 1983-08-31 | 1985-03-19 | Nippon Kokan Kk <Nkk> | Surface treated steel sheet having high resistance to corrosion |
-
1986
- 1986-03-27 JP JP6985286A patent/JPS62225341A/en active Pending
Patent Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5342150A (en) * | 1976-09-30 | 1978-04-17 | Kawatetsu Galvanizing | Zinced steel sheet applied with primer coating which is spottweldable |
JPS5461277A (en) * | 1977-10-25 | 1979-05-17 | Kawatetsu Kohan Kk | Anticorrosive coated steel plate with good pressing processability |
JPS54112731A (en) * | 1978-02-24 | 1979-09-03 | Toyo Kohan Co Ltd | Composite covered steel plate |
JPS598354A (en) * | 1982-07-06 | 1984-01-17 | Matsushita Electronics Corp | Formation of metal film wiring |
JPS59171645A (en) * | 1983-03-19 | 1984-09-28 | 日新製鋼株式会社 | Weldable coated steel plate having excellent corrosion protection |
JPS6050181A (en) * | 1983-08-31 | 1985-03-19 | Nippon Kokan Kk <Nkk> | Surface treated steel sheet having high resistance to corrosion |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4959277A (en) * | 1988-12-07 | 1990-09-25 | Nihon Parkerizing Co., Ltd. | Process for treating plated steel sheet |
US5968662A (en) * | 1995-03-08 | 1999-10-19 | Nisshin Steel Co., Ltd. | Coated metal sheet bondable with adhesive |
JP2005271519A (en) * | 2004-03-26 | 2005-10-06 | Matsushita Electric Ind Co Ltd | Surface-treated steel plate and cooking device using it |
JP4670248B2 (en) * | 2004-03-26 | 2011-04-13 | パナソニック株式会社 | Cooker using surface-treated steel sheet |
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