JPH04210275A - Formation of coating film - Google Patents
Formation of coating filmInfo
- Publication number
- JPH04210275A JPH04210275A JP34095490A JP34095490A JPH04210275A JP H04210275 A JPH04210275 A JP H04210275A JP 34095490 A JP34095490 A JP 34095490A JP 34095490 A JP34095490 A JP 34095490A JP H04210275 A JPH04210275 A JP H04210275A
- Authority
- JP
- Japan
- Prior art keywords
- resin
- paint
- coating film
- chrome
- surface tension
- 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
Links
- 238000000576 coating method Methods 0.000 title claims abstract description 23
- 239000011248 coating agent Substances 0.000 title claims abstract description 22
- 230000015572 biosynthetic process Effects 0.000 title description 4
- 229920005989 resin Polymers 0.000 claims abstract description 46
- 239000011347 resin Substances 0.000 claims abstract description 46
- 239000003973 paint Substances 0.000 claims abstract description 39
- 125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 claims abstract description 16
- 238000000034 method Methods 0.000 claims abstract description 9
- 229920005749 polyurethane resin Polymers 0.000 claims abstract description 8
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 claims description 25
- 239000007788 liquid Substances 0.000 claims 1
- 239000000356 contaminant Substances 0.000 abstract description 5
- 229920000728 polyester Polymers 0.000 abstract description 5
- 239000003822 epoxy resin Substances 0.000 abstract description 4
- 229920000647 polyepoxide Polymers 0.000 abstract description 4
- 229920000098 polyolefin Polymers 0.000 abstract description 4
- 229920006311 Urethane elastomer Polymers 0.000 abstract description 3
- 239000004844 aliphatic epoxy resin Substances 0.000 abstract description 3
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 abstract description 3
- 229920000915 polyvinyl chloride Polymers 0.000 abstract 1
- 238000007747 plating Methods 0.000 description 22
- 239000000463 material Substances 0.000 description 8
- 230000007423 decrease Effects 0.000 description 7
- 238000012360 testing method Methods 0.000 description 6
- 238000001035 drying Methods 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- 239000000049 pigment Substances 0.000 description 4
- 229920002635 polyurethane Polymers 0.000 description 4
- 239000004814 polyurethane Substances 0.000 description 4
- 229920002554 vinyl polymer Polymers 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- 239000004925 Acrylic resin Substances 0.000 description 3
- 229920000178 Acrylic resin Polymers 0.000 description 3
- 238000010422 painting Methods 0.000 description 3
- 229920001225 polyester resin Polymers 0.000 description 3
- 239000004645 polyester resin Substances 0.000 description 3
- 239000004606 Fillers/Extenders Substances 0.000 description 2
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical class OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 2
- 239000004721 Polyphenylene oxide Substances 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 238000004040 coloring Methods 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 238000007654 immersion Methods 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 238000011056 performance test Methods 0.000 description 2
- 229920003023 plastic Polymers 0.000 description 2
- 239000004033 plastic Substances 0.000 description 2
- 229920000570 polyether Polymers 0.000 description 2
- 239000005056 polyisocyanate Substances 0.000 description 2
- 229920001228 polyisocyanate Polymers 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 229920005862 polyol Polymers 0.000 description 2
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 2
- MTZUIIAIAKMWLI-UHFFFAOYSA-N 1,2-diisocyanatobenzene Chemical compound O=C=NC1=CC=CC=C1N=C=O MTZUIIAIAKMWLI-UHFFFAOYSA-N 0.000 description 1
- UPMLOUAZCHDJJD-UHFFFAOYSA-N 4,4'-Diphenylmethane Diisocyanate Chemical compound C1=CC(N=C=O)=CC=C1CC1=CC=C(N=C=O)C=C1 UPMLOUAZCHDJJD-UHFFFAOYSA-N 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- 239000005057 Hexamethylene diisocyanate Substances 0.000 description 1
- 239000005058 Isophorone diisocyanate Substances 0.000 description 1
- QORUGOXNWQUALA-UHFFFAOYSA-N N=C=O.N=C=O.N=C=O.C1=CC=C(C(C2=CC=CC=C2)C2=CC=CC=C2)C=C1 Chemical compound N=C=O.N=C=O.N=C=O.C1=CC=C(C(C2=CC=CC=C2)C2=CC=CC=C2)C=C1 QORUGOXNWQUALA-UHFFFAOYSA-N 0.000 description 1
- 235000010582 Pisum sativum Nutrition 0.000 description 1
- 240000004713 Pisum sativum Species 0.000 description 1
- 230000005856 abnormality Effects 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- -1 acrylic polyols Chemical class 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- KIQKWYUGPPFMBV-UHFFFAOYSA-N diisocyanatomethane Chemical compound O=C=NCN=C=O KIQKWYUGPPFMBV-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000007772 electroless plating Methods 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 230000009477 glass transition Effects 0.000 description 1
- 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 1
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 1
- 239000011229 interlayer Substances 0.000 description 1
- NIMLQBUJDJZYEJ-UHFFFAOYSA-N isophorone diisocyanate Chemical compound CC1(C)CC(N=C=O)CC(C)(CN=C=O)C1 NIMLQBUJDJZYEJ-UHFFFAOYSA-N 0.000 description 1
- 239000004922 lacquer Substances 0.000 description 1
- 239000010410 layer Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000002923 metal particle Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- AYLRODJJLADBOB-QMMMGPOBSA-N methyl (2s)-2,6-diisocyanatohexanoate Chemical compound COC(=O)[C@@H](N=C=O)CCCCN=C=O AYLRODJJLADBOB-QMMMGPOBSA-N 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 229920005906 polyester polyol Polymers 0.000 description 1
- 229920006124 polyolefin elastomer Polymers 0.000 description 1
- 229920005672 polyolefin resin Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000002987 primer (paints) Substances 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 229920005992 thermoplastic resin Polymers 0.000 description 1
- DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Abstract
Description
【発明の詳細な説明】
[産業上の利用分野]
本発明は金属、プラスチック等の種々の基材上に形成さ
れたクロムメツキ面に付着性及び耐候性のすぐれた塗膜
を形成する方法に関する。DETAILED DESCRIPTION OF THE INVENTION [Industrial Application Field] The present invention relates to a method for forming a coating film with excellent adhesion and weather resistance on a chrome plated surface formed on various base materials such as metals and plastics.
種々の基材上にクロムメツキが行われていることは周知
である。又かかるクロムメツキ面を塗料で塗装すること
も知られている。It is well known that chrome plating is performed on a variety of substrates. It is also known to paint such chrome-plated surfaces with paint.
しかしながら一般にクロムメツキしたとき、その面は汚
れが残り易く、或いはメツキの経時変化による活性度の
劣化により、クロムメツキ面に塗料塗膜を形成したとき
、かかるクロムメツキ面に対する付着性のすぐれた塗膜
を形成することが難しく、付着性にばらつきが生じ易い
。However, when chrome plating is applied, dirt tends to remain on the surface, or the activity of the plating deteriorates over time, so when a paint film is formed on the chrome plating surface, it forms a paint film with excellent adhesion to the chrome plating surface. It is difficult to do so and tends to cause variations in adhesion.
クロムメツキされた材料は自動車等で外部に直接曝され
る部分に多用され、その上に更に塗料塗膜を塗布するこ
とにより一層耐久性を向上させるようになって来ている
。Chrome-plated materials are often used in parts of automobiles and the like that are directly exposed to the outside, and their durability is further improved by coating them with a coating of paint.
従来基材例えばプラスチック基村上にクロムメツキをし
、このクロムメツキ面を塗装するに当っては、クロムメ
ツキをした後短時間の内に、通常のラッカーを塗装する
か或いは2液型ポリウレタン樹脂塗料を塗装する方法が
一般に行われている。その理由はクロムメツキをした後
、形成されたクロムメツキ面の経時変化が少ない内に塗
装すれば比較的安定した状態の塗膜が形成できるからで
ある。Conventionally, when chrome plating is applied to a base material such as plastic, and the chrome plating surface is painted, a normal lacquer or two-component polyurethane resin paint is applied within a short period of time after chrome plating. The method is commonly used. The reason for this is that after chrome plating, if the coating is applied while the chrome plating surface has little change over time, a relatively stable coating film can be formed.
[発明が解決しようとする課題]
従来クロムメツキ面は、その形成条件により例えば洗浄
水、酸その他の汚染物による汚れ量が多くなることがあ
り、或いはメツキ層の厚さが異なるメツキ面又はメツキ
形成後5日以上経過したメツキ面等では、塗料との付着
性が低下し、メツキ面と塗膜の界面にて塗膜が剥離する
問題がしばしば生じている。[Problems to be Solved by the Invention] Conventionally, a chrome-plated surface may have a large amount of dirt due to cleaning water, acid, or other contaminants depending on the formation conditions, or a plating surface with a different thickness of the plating layer or a plating formation On a plated surface that has been used for more than 5 days, the adhesion with the paint decreases, and the problem often arises that the coating film peels off at the interface between the plated surface and the coating film.
本来クロムメツキ面は表面張力が小さく、又メツキ表面
の状態も充分に解明されておらず、このため塗膜は付着
し難い傾向を有している。従来の塗料による塗膜形成法
の中、2液型ポリウレタン樹脂塗料では、ポリオール成
分の構造を変えることにより、クロムメツキ形成後比較
的初期の段階では、塗料塗膜の付着性は改良されて、剥
離は少なくなっている。しかしながらクロムメツキ面の
経時変化の如き変化が大きい場合、又はポリウレタン樹
脂が劣化し易い条件下では、この塗料による塗膜にも剥
離が生ずるため、屋外用途等の厳しい条件での使用には
不充分であった。The surface tension of a chrome plated surface is originally low, and the condition of the plated surface is not fully understood, so that paint films tend to be difficult to adhere to. Among the conventional coating film forming methods using paints, two-component polyurethane resin paints improve the adhesion of the paint film at a relatively early stage after chrome plating by changing the structure of the polyol component, making it easier to peel off. is decreasing. However, if the chrome plating surface undergoes large changes over time, or under conditions where the polyurethane resin easily deteriorates, the paint film will peel, making it insufficient for use in harsh conditions such as outdoor applications. there were.
[課題を解決するための手段]
本発明者等はクロムメツキ面への塗料塗膜の付着性につ
いて鋭意研究を重ねた結果、後述するような特定の表面
張力、特定の伸び率及び特定の組成を有する樹脂又は樹
脂混合物を含有する塗料を下ff1ffi料として用い
、クロムメツキ面を塗装することにより、前記従来の問
題点を解決できることを見出した。[Means for Solving the Problem] As a result of extensive research into the adhesion of paint films to chrome plating surfaces, the present inventors have determined that a specific surface tension, a specific elongation rate, and a specific composition as described below. It has been found that the above-mentioned conventional problems can be solved by using a paint containing a resin or a resin mixture as a lower ff1ffi material and painting a chrome-plated surface.
本発明はクロムメツキ面に、(1)表面張力が20〜3
2 dyne/ cm、 Tgが一10℃〜10℃、塗
膜伸び率が80%以上でかつグリシジル基を有する樹脂
(A)を含有する下塗塗料、又は(2)表面張力が20
〜32 dyne/ cm、 Tgが一10℃〜10℃
、塗膜伸び率が80%以上の樹脂(B)及びグリシジル
基を有する樹脂(C)を含有する下塗塗料を塗装し、次
いで上塗として2液型ポリウレタン樹脂塗料を塗装する
塗膜の形成方法にある。In the present invention, the chrome plated surface has (1) a surface tension of 20 to 3;
2 dyne/cm, a Tg of 110°C to 10°C, a coating elongation rate of 80% or more, and an undercoat containing a resin (A) having a glycidyl group, or (2) a surface tension of 20°C.
~32 dyne/cm, Tg -10℃~10℃
, a method of forming a coating film by applying an undercoat containing a resin (B) with a coating elongation rate of 80% or more and a resin (C) having a glycidyl group, and then applying a two-component polyurethane resin coating as a topcoat. be.
本発明はクロムメツキ面を塗装するに当り、クロムメツ
キ面の表面張力が小さい点に着目し、その表面張力に近
似した表面張力即ち20〜32dyne/cmの表面張
力を有する樹脂を用い、しかも塗膜の硬化応力歪を緩和
させるため、樹脂の伸び率を通常の硬質素材に要求され
る下塗塗料塗膜の伸び率より大きくした即ち80%以上
の伸び率を有する樹脂を含む下塗塗料を用いることによ
って、クロムメツキ面、特にその面の経時変化があって
もそれに対する付着性の低下を生じさせぬようにしたの
である。When painting a chrome-plated surface, the present invention focuses on the fact that the surface tension of the chrome-plated surface is small, and uses a resin that has a surface tension close to that surface tension, that is, a surface tension of 20 to 32 dyne/cm. In order to alleviate the curing stress strain, the elongation rate of the resin is made larger than the elongation rate of the undercoat paint film required for ordinary hard materials, that is, by using an undercoat paint containing a resin with an elongation rate of 80% or more. This was done so that the adhesion to the chrome plated surface, especially that surface, would not deteriorate even if the surface changed over time.
又前述した如く、クロムメツキ面には種々の汚染物、例
えば水分、他の金属異物、更にはメツキ面形成時に使用
される酸性成分などが存在することがあり、これらが下
塗塗料のクロムメツキ面への付着性を低下させる要因と
なっている。これに対し本発明では下mW料に用いる樹
脂にグリシジル基を有する樹脂(A)、又は樹脂混合物
[樹脂(C)を含む〕を用いることによって上記汚染物
が存在してもクロムメツキ面への結合力を低下させず、
安定した付着力を発揮させるようにしたのである。Furthermore, as mentioned above, there may be various contaminants on the chrome-plated surface, such as moisture, other foreign metal particles, and even acidic components used in forming the chrome-plated surface. This is a factor that reduces adhesion. In contrast, in the present invention, by using a resin (A) having a glycidyl group or a resin mixture [containing resin (C)] as the resin used for the lower mW material, even if the above contaminants are present, the bonding to the chrome plating surface is prevented. without reducing power,
This was done to ensure stable adhesion.
本発明によれば、前述した特定の下塗塗料を塗装した後
、上塗として2液型ポリウレタン樹脂塗料を塗装するこ
とによって、形成された塗膜に耐候性をもたせるのであ
る。According to the present invention, after applying the above-mentioned specific undercoat paint, a two-component polyurethane resin paint is applied as a top coat, thereby imparting weather resistance to the formed paint film.
本発明で対象とするクロムメツキ面は、通常の金属基材
はもちろんのこと、メツキ用品種の樹脂基村上に、当業
者に知られている通常の方法、例えば無電解メツキ法等
で形成された任意のクロムメツキ面である。The chrome plating surface that is the object of the present invention can be formed not only on a regular metal base material but also on a resin base plate for plating products by a conventional method known to those skilled in the art, such as an electroless plating method. Any chrome plated surface.
本発明の下塗塗料で用いる前記樹脂(A)は、前述した
表面張力、伸び率、Tgを有し、かつグリシジル基を有
する樹脂であれば任意の樹脂を使用でき、例えばポリビ
ニル、ポリオレフィン、ポリエステル系のグリシジル基
を有する樹脂を挙げることができる。The resin (A) used in the undercoat of the present invention can be any resin as long as it has the surface tension, elongation, and Tg described above and has a glycidyl group, such as polyvinyl, polyolefin, and polyester. Examples include resins having glycidyl groups.
又本発明の下塗塗料で用いる前記樹脂(B)は前述した
表面張力、伸び率及びTgを有する樹脂であれば任意の
樹脂を使用でき、例えばポリビニル、ポリエステル、ポ
リエーテル、ポリオレフィン、ウレタンエラストマー系
の樹脂を使用できる。Further, as the resin (B) used in the undercoat of the present invention, any resin can be used as long as it has the above-mentioned surface tension, elongation rate, and Tg, such as polyvinyl, polyester, polyether, polyolefin, and urethane elastomer. Resin can be used.
上記樹脂(B)と共に用いるグリシジル基を有する樹脂
(C)としてはフェノール系エポキシ樹脂、脂肪族系エ
ポキシ樹脂を使用できる。As the resin (C) having a glycidyl group used together with the resin (B), phenolic epoxy resins and aliphatic epoxy resins can be used.
前記樹脂(A)及び(B)の表面張力は20〜32 d
yne/ cmの範囲が好ましい。The surface tension of the resins (A) and (B) is 20 to 32 d.
A range of yne/cm is preferred.
又塗膜伸び率は80%以上有すること、好まし7くは1
00〜160%にする、又Tgは一10°C〜10℃を
有するようにする。Also, the coating film elongation rate should be 80% or more, preferably 7 or 1.
00-160%, and Tg should be -10°C to 10°C.
本発明によれば前記樹脂(A)、及び樹脂(B)と混用
する樹脂(C)にはグリシジル基を有するものを使用す
る。この場合樹脂(A)中のグリシジル基の含有率、及
び樹脂(B)と樹脂(C)の合計量に対する樹脂(C)
に含まれるグリシジル基の含有率は5%(mol )以
上で15%(mol)以下とするとよい。上記グリシジ
ル基の含有率が5%(mol )より小さくなると、ク
ロムメツキ面、特にメツキ面に汚染物が存在するとき、
又はメツキ後例えば5日以上たって経時変化したとき、
付着性が低下し好ましくない、又15%(mol)より
大となると乾燥性が低下し好ましくない。According to the present invention, the resin (A) and the resin (C) used in combination with the resin (B) are those having a glycidyl group. In this case, the content of glycidyl groups in the resin (A) and the resin (C) relative to the total amount of the resin (B) and the resin (C)
The content of glycidyl groups contained in is preferably 5% (mol) or more and 15% (mol) or less. When the content of the glycidyl group is less than 5% (mol), when contaminants are present on the chrome plated surface, especially on the plated surface,
Or when there is a change over time, for example 5 days or more after plating,
Adhesiveness decreases, which is undesirable, and if it exceeds 15% (mol), drying properties decrease, which is undesirable.
本発明の下塗塗料に用いる樹脂(A)及び(B)の表面
張力が20dyne/cmより小さくなればなる程、或
いは32 dyne/ cmを越えれば越える程、クロ
ムメツキ面との表面張力の差が大となり、塗膜面とクロ
ムメツキ面との親和性が低下し、結果として付着性の劣
化を伴うので好ましくない。The smaller the surface tension of resins (A) and (B) used in the primer coating of the present invention is below 20 dyne/cm, or the greater it exceeds 32 dyne/cm, the greater the difference in surface tension with the chrome-plated surface. This is not preferable because the affinity between the coated film surface and the chrome-plated surface decreases, resulting in deterioration of adhesion.
又伸び率が80%未満になると、塗膜形成時の内部応力
が高くなり、付着性の低下を生じるので好ましくない。Moreover, if the elongation rate is less than 80%, internal stress during coating film formation becomes high, resulting in a decrease in adhesion, which is not preferable.
又前記樹脂(A)及び(B)はガラス転移温度(Tg)
が−10℃〜10℃のものを使用するとよい。これらの
樹脂のTgが一10℃より低くなると、これらの下塗塗
料塗膜の上に2液型ポリウレタン塗料を塗装しても得ら
れる塗膜の硬度が小さくなって好ましくなく、又Tgが
10℃より高くなると下塗塗膜の伸び率80%以上が得
難くなると共に、メツキ面上での塗膜形成時の塗膜硬化
歪が生じ易くなり、付着力が低下するので好ましくない
本発明で使用する下塗塗料は、(1)前記特定の樹脂(
A)、又は(2)前記特定の樹脂(B)及び樹脂(C)
の外に有機溶剤を主成分として含有し、更に所望によっ
て着色顔料、体質顔料、通常使用される他の添加剤を配
合できる。Further, the resins (A) and (B) have a glass transition temperature (Tg)
It is preferable to use one with a temperature of -10°C to 10°C. If the Tg of these resins is lower than -10°C, the hardness of the resulting paint film will be undesirable even if a two-component polyurethane paint is applied on top of these undercoat paint films, and this is not preferable. If it is higher, it will be difficult to obtain an elongation rate of 80% or more for the undercoat film, and it will also be easy to cause distortion in the curing of the paint film when forming the paint film on the glazed surface, resulting in a decrease in adhesion, which is not preferable for use in the present invention. The undercoat paint contains (1) the above-mentioned specific resin (
A) or (2) the specific resin (B) and resin (C)
In addition to this, it contains an organic solvent as a main component, and if desired, coloring pigments, extender pigments, and other commonly used additives can be added.
前記下塗塗料は通常使用される塗装方法で塗装できる。The undercoat paint can be applied by a commonly used coating method.
本発明によれば前記下塗塗料塗装後、湿潤状態で、又は
通常40〜100℃で20〜60分乾燥した後、形成さ
れた下塗塗膜上に2液型ポリウレタン塗料を塗装する。According to the present invention, after the undercoat is applied, a two-component polyurethane paint is applied on the formed undercoat film in a wet state or after drying for 20 to 60 minutes, usually at 40 to 100°C.
本発明に用いられる樹脂(A)としてはビニル系、ポリ
オレフィン系、ポリエステル系のグリシジル基含有ポリ
マーかが適しており樹脂CB)としてはビニル系、ポリ
エステル系、ポリエーテル系、ポリオレフィン系、ウレ
タンエラストマー系が好ましい。更に樹脂(C)として
はフェノール系エポキシ樹脂、脂肪族系エポキシ樹脂な
どが用いられる。又表面張力は20 dyne/ am
より小さいと上塗塗料を塗装する場合層間付着性を低下
させ、1間剥離を生じやすくなり又32 dyne/
cmより大きいとメツキ面の濡れ性が低下し素材との付
着性を悪くする。Suitable resins (A) used in the present invention are vinyl-based, polyolefin-based, and polyester-based glycidyl group-containing polymers, and resins CB) are vinyl-based, polyester-based, polyether-based, polyolefin-based, and urethane elastomer-based polymers. is preferred. Further, as the resin (C), phenolic epoxy resin, aliphatic epoxy resin, etc. are used. Also, the surface tension is 20 dyne/am
If it is smaller, the interlayer adhesion will be lowered when applying the top coat, and peeling will occur more easily.
If it is larger than cm, the wettability of the plating surface will decrease and the adhesion to the material will deteriorate.
本発明において用いられるクロムメツキ板は、メツキ用
グレートのABSなどの上に通常の工程で行われるクロ
ムメツキ一般を意味している。The chrome-plated plate used in the present invention refers to a general chrome-plated plate that is applied on a plating plate, such as ABS, in a normal process.
下塗塗料は、ビヒクル成分と有機溶剤を主成分とし、こ
れにさらに必要に応じて着色顔料、体質顔料、その他の
添加剤などを配合することができる。The undercoating paint has a vehicle component and an organic solvent as its main components, and may further contain coloring pigments, extender pigments, other additives, etc. as necessary.
上記ビヒクル成分は熱可塑性樹脂であっても、叶基を有
し、硬化剤としてポリイソシアネートを用いる2液ウレ
タン系であっても上記範囲内にあれば適するものである
。この時用いられるポリイソシアネートはトルエンジイ
ソシアネート、ジフェニルメタンジイソシアネート、メ
チレンジイソシアネート、キシレンジイソシアネート、
ヘキサメチレン−ジイソシアネート、イソホロンジイソ
シアネート、トリフェニルメタントリイソシアネート、
フェニレンジイソシアネート、リジンジイソシアネート
、及び上記のメチロール付加物又は3−5ji体など更
にはこれらの混合物が適している。The vehicle component is suitable even if it is a thermoplastic resin or a two-component urethane system having a leaf group and using polyisocyanate as a curing agent, as long as it is within the above range. The polyisocyanates used at this time include toluene diisocyanate, diphenylmethane diisocyanate, methylene diisocyanate, xylene diisocyanate,
Hexamethylene diisocyanate, isophorone diisocyanate, triphenylmethane triisocyanate,
Suitable are phenylene diisocyanate, lysine diisocyanate, the above-mentioned methylol adducts or 3-5ji derivatives, and mixtures thereof.
更に、下塗塗料は塗装後ウェットの状態であるいは40
℃〜100℃×20〜60分の乾燥後、上塗を塗装して
も良い。Furthermore, the undercoat should be applied in a wet state after painting or
After drying for 20 to 60 minutes at 100°C to 100°C, a top coat may be applied.
一方上塗として用いられる塗料は一般の2液のポリウレ
タン塗料であれば良く、特にアクリルポリオール、ポリ
エステルポリオールが望ましく、50〜100′CX2
0〜100分の乾燥条件が適している。On the other hand, the paint used as the top coat may be any general two-component polyurethane paint, and acrylic polyols and polyester polyols are particularly preferred, and 50-100'CX2
Drying conditions of 0 to 100 minutes are suitable.
[実施例] 以下に実施例を挙げて本発明を説明する。[Example] The present invention will be explained below with reference to Examples.
実施例
■、試料の調整
(1)クロムメツキ板
(イ) ABS上のクロムメッキ板5日以上経過品(日
本テストパネル社製)
(ロ) ABS上クワクロムメツキ板ツキ液を1部濃度
にて全面スプレーした板
(2)ブライマー(いずれも重量部を示す)(a)グリ
シジル含有ポリオレフィン樹脂(旭電化製LPM 65
0−50X、 Tg: 0℃、表面張カニ 26 dy
ne/ cm、伸び率 250%)に酸化チタン20部
、キジロール60部よりなる塗料
(b)ポリエステル樹脂(東洋紡製バイロン500、T
g:4℃、表面張力 26 dyne/ cm、伸び率
・1100%)100部をメチルエチルケトン70部、
キジロール70部に溶解した溶液にエピコート828(
シェル化学製エポキシ樹脂)10部、酸化チタン20部
、キジロール50部よりなる塗料
(C)上記(b)でエピコート828を0部にした塗料
(d)上記(b)でポリエステル樹脂(バイロン500
)の代りにアクリル樹脂(I) (7g15℃、表面
張力38 dyne/ cm、伸び率30%)を用いた
塗料
(e)上記(b)でポリエステル樹脂(バイロン500
)の代りにアクリル樹脂(II) (7g8℃、表面
張力38 dyne/ cm、伸び率85%)を用いた
塗料
(3)上塗塗料
2液ポリウレタン樹脂塗料・ボリン隘1黒(神東塗料製
アクリルポリウレタン塗料)(4)アクリル樹脂(I)
、(rI)の組成(5)ブライマー塗料の製造法
それぞれの樹脂と酸化チタンと溶剤を全量20分間均一
に攪拌した後ペイントコンディショナーで30分間分散
を行い粒度10μ以下になっていることを確認した後ガ
ラスピーズを濾過し塗料とする。Example ■, Sample preparation (1) Chrome plated plate (a) Chrome plated plate on ABS that has been used for more than 5 days (manufactured by Japan Test Panel Co., Ltd.) (b) Chrome plated plate on ABS at a concentration of 1 part Fully sprayed plate (2) Brimer (all parts by weight are shown) (a) Glycidyl-containing polyolefin resin (LPM 65 manufactured by Asahi Denka Co., Ltd.)
0-50X, Tg: 0℃, surface tension crab 26 dy
(b) Polyester resin (Toyobo Vylon 500, T
g: 4°C, surface tension 26 dyne/cm, elongation rate 1100%) 100 parts, 70 parts methyl ethyl ketone,
Epicoat 828 (
(C) Paint consisting of 10 parts of Shell Chemical's epoxy resin), 20 parts of titanium oxide, and 50 parts of Kijiroll (C) Paint with 0 parts of Epicoat 828 in (b) above (d) Polyester resin (Vylon 500) in (b) above
) instead of acrylic resin (I) (7g 15℃, surface tension 38 dyne/cm, elongation rate 30%) (e) In the above (b), polyester resin (Vylon 500
) Paint using acrylic resin (II) (7g8℃, surface tension 38 dyne/cm, elongation rate 85%) Polyurethane paint) (4) Acrylic resin (I)
Composition of (rI) (5) Manufacturing method of brimer paint The total amount of each resin, titanium oxide, and solvent was stirred uniformly for 20 minutes, then dispersed for 30 minutes with a paint conditioner, and it was confirmed that the particle size was 10μ or less. The glass peas are then filtered and used as paint.
H、実施例、比較例
上記工で調整した試料を用いて
クロムメツキ板−ブライマー(10μ)−5分インター
バル−上塗(30μ)−乾燥80℃X30分
の工程で表−1に示す組合せで塗装した。H. Examples and Comparative Examples The samples prepared in the above process were coated using the combinations shown in Table 1 in the following steps: chrome plated board - brimer (10μ) - 5 minute intervals - topcoat (30μ) - drying at 80°C for 30 minutes. .
■、性能試験結果
上記実施例、比較例において塗装した塗板を用いて性能
試験を行った結果を表−2に示す。(2) Performance test results Table 2 shows the results of a performance test using the coated plates coated in the above Examples and Comparative Examples.
(試験方法)
■付着性:1m/mゴバン目テスト
■温水性:80℃X120t(r温水浸漬テスト後の付
着性テスト
温水浸漬テスト後の付着性テスト
(評 価)
0 異常なし
×、パクリあり
\(Test method) ■Adhesiveness: 1m/m grid test ■Warm water resistance: 80°C x 120t (r Adhesion test after hot water immersion test Adhesion test after warm water immersion test (evaluation) 0 No abnormalities ×, plagiarism \
Claims (1)
yne/cm、Tgが−10℃〜10℃、塗膜伸び率が
80%以上でかつグリシジル基を有する樹脂(A)を含
有する下塗塗料、又は(2)表面張力が20〜32dy
ne/cm、Tgが−10℃〜10℃、塗膜伸び率が8
0%以上の樹脂(B)及びグリシジル基を有する樹脂(
C)を含有する下塗塗料を塗装し、次いで上塗として2
液型ポリウレタン樹脂塗料を塗装することを特徴とする
塗膜の形成方法1. The chrome plated surface has (1) a surface tension of 20 to 32 d.
yne/cm, Tg is -10°C to 10°C, a coating film elongation rate is 80% or more, and an undercoat containing a resin (A) having a glycidyl group, or (2) a surface tension of 20 to 32 dy.
ne/cm, Tg is -10°C to 10°C, coating elongation rate is 8
0% or more of resin (B) and resin having glycidyl group (
Apply a base coat containing C) and then apply 2 as a top coat.
A method for forming a coating film characterized by applying a liquid polyurethane resin paint
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP34095490A JPH0710375B2 (en) | 1990-11-30 | 1990-11-30 | Method of forming coating film |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP34095490A JPH0710375B2 (en) | 1990-11-30 | 1990-11-30 | Method of forming coating film |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH04210275A true JPH04210275A (en) | 1992-07-31 |
JPH0710375B2 JPH0710375B2 (en) | 1995-02-08 |
Family
ID=18341841
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP34095490A Expired - Lifetime JPH0710375B2 (en) | 1990-11-30 | 1990-11-30 | Method of forming coating film |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0710375B2 (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2007536405A (en) * | 2004-05-02 | 2007-12-13 | アシュランド・ライセンシング・アンド・インテレクチュアル・プロパティー・エルエルシー | Radiation curable coatings for plastic substrates from polyfunctional acrylate oligomers |
JP2016123916A (en) * | 2014-12-26 | 2016-07-11 | 株式会社ファルテック | Method for forming coating film, coating film, and coated article |
-
1990
- 1990-11-30 JP JP34095490A patent/JPH0710375B2/en not_active Expired - Lifetime
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2007536405A (en) * | 2004-05-02 | 2007-12-13 | アシュランド・ライセンシング・アンド・インテレクチュアル・プロパティー・エルエルシー | Radiation curable coatings for plastic substrates from polyfunctional acrylate oligomers |
JP2016123916A (en) * | 2014-12-26 | 2016-07-11 | 株式会社ファルテック | Method for forming coating film, coating film, and coated article |
Also Published As
Publication number | Publication date |
---|---|
JPH0710375B2 (en) | 1995-02-08 |
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