JPH03287679A - Primer composition for phenolic resin - Google Patents
Primer composition for phenolic resinInfo
- Publication number
- JPH03287679A JPH03287679A JP9074090A JP9074090A JPH03287679A JP H03287679 A JPH03287679 A JP H03287679A JP 9074090 A JP9074090 A JP 9074090A JP 9074090 A JP9074090 A JP 9074090A JP H03287679 A JPH03287679 A JP H03287679A
- Authority
- JP
- Japan
- Prior art keywords
- phenolic resin
- primer
- urethane polyol
- polyisocyanate prepolymer
- component
- 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
- 239000000203 mixture Substances 0.000 title claims abstract description 16
- 239000005011 phenolic resin Substances 0.000 title claims abstract description 16
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 title claims abstract description 15
- 229920001568 phenolic resin Polymers 0.000 title claims abstract description 15
- 229920005862 polyol Polymers 0.000 claims abstract description 23
- -1 urethane polyol Chemical class 0.000 claims abstract description 18
- 239000005056 polyisocyanate Substances 0.000 claims abstract description 14
- 229920001228 polyisocyanate Polymers 0.000 claims abstract description 14
- 239000000049 pigment Substances 0.000 claims abstract description 11
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 8
- 239000007787 solid Substances 0.000 claims abstract description 7
- 238000000465 moulding Methods 0.000 abstract 2
- 239000005002 finish coating Substances 0.000 abstract 1
- 239000003973 paint Substances 0.000 description 21
- 239000002987 primer (paints) Substances 0.000 description 18
- 238000012360 testing method Methods 0.000 description 10
- 238000000576 coating method Methods 0.000 description 9
- 239000011248 coating agent Substances 0.000 description 7
- 150000003077 polyols Chemical class 0.000 description 6
- 239000000654 additive Substances 0.000 description 4
- 229920000180 alkyd Polymers 0.000 description 4
- 238000013461 design Methods 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 239000004606 Fillers/Extenders Substances 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 238000011161 development Methods 0.000 description 3
- 238000011156 evaluation Methods 0.000 description 3
- 239000012948 isocyanate Substances 0.000 description 3
- 150000002513 isocyanates Chemical class 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 238000010422 painting Methods 0.000 description 3
- 238000004383 yellowing Methods 0.000 description 3
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- 239000004593 Epoxy Substances 0.000 description 2
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 2
- 239000005058 Isophorone diisocyanate Substances 0.000 description 2
- 229920000877 Melamine resin Polymers 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 2
- 238000000889 atomisation Methods 0.000 description 2
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 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 2
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 2
- 229920001515 polyalkylene glycol Polymers 0.000 description 2
- 229920005906 polyester polyol Polymers 0.000 description 2
- 239000004814 polyurethane Substances 0.000 description 2
- 229920002635 polyurethane Polymers 0.000 description 2
- 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 2
- FKTHNVSLHLHISI-UHFFFAOYSA-N 1,2-bis(isocyanatomethyl)benzene Chemical compound O=C=NCC1=CC=CC=C1CN=C=O FKTHNVSLHLHISI-UHFFFAOYSA-N 0.000 description 1
- 229920000298 Cellophane Polymers 0.000 description 1
- 239000000020 Nitrocellulose Substances 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- NRCMAYZCPIVABH-UHFFFAOYSA-N Quinacridone Chemical compound N1C2=CC=CC=C2C(=O)C2=C1C=C1C(=O)C3=CC=CC=C3NC1=C2 NRCMAYZCPIVABH-UHFFFAOYSA-N 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- UKLDJPRMSDWDSL-UHFFFAOYSA-L [dibutyl(dodecanoyloxy)stannyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCCCCCC UKLDJPRMSDWDSL-UHFFFAOYSA-L 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 239000005456 alcohol based solvent Substances 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- HIFVAOIJYDXIJG-UHFFFAOYSA-N benzylbenzene;isocyanic acid Chemical class N=C=O.N=C=O.C=1C=CC=CC=1CC1=CC=CC=C1 HIFVAOIJYDXIJG-UHFFFAOYSA-N 0.000 description 1
- 230000001588 bifunctional effect Effects 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 239000007809 chemical reaction catalyst Substances 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- XCJYREBRNVKWGJ-UHFFFAOYSA-N copper(II) phthalocyanine Chemical compound [Cu+2].C12=CC=CC=C2C(N=C2[N-]C(C3=CC=CC=C32)=N2)=NC1=NC([C]1C=CC=CC1=1)=NC=1N=C1[C]3C=CC=CC3=C2[N-]1 XCJYREBRNVKWGJ-UHFFFAOYSA-N 0.000 description 1
- 238000005034 decoration Methods 0.000 description 1
- 239000012975 dibutyltin dilaurate Substances 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 125000005442 diisocyanate group Chemical group 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- 239000004205 dimethyl polysiloxane Substances 0.000 description 1
- 235000013870 dimethyl polysiloxane Nutrition 0.000 description 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 125000004836 hexamethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[*:1] 0.000 description 1
- 150000002483 hydrogen compounds Chemical class 0.000 description 1
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 1
- ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Chemical group OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 239000004922 lacquer Substances 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- GEMHFKXPOCTAIP-UHFFFAOYSA-N n,n-dimethyl-n'-phenylcarbamimidoyl chloride Chemical compound CN(C)C(Cl)=NC1=CC=CC=C1 GEMHFKXPOCTAIP-UHFFFAOYSA-N 0.000 description 1
- 229920001220 nitrocellulos Polymers 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- IEQIEDJGQAUEQZ-UHFFFAOYSA-N phthalocyanine Chemical compound N1C(N=C2C3=CC=CC=C3C(N=C3C4=CC=CC=C4C(=N4)N3)=N2)=C(C=CC=C2)C2=C1N=C1C2=CC=CC=C2C4=N1 IEQIEDJGQAUEQZ-UHFFFAOYSA-N 0.000 description 1
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
Abstract
Description
【発明の詳細な説明】
産業上の利用分野
本発明はフェノール樹脂成形品に各種の塗装、装飾が成
される際のプライマー組成物に関する。DETAILED DESCRIPTION OF THE INVENTION Field of Industrial Application The present invention relates to a primer composition for applying various coatings and decorations to phenolic resin molded articles.
さらに詳しくは、密着性の問題から無塗装のまま使用さ
れることが多かったフェノール樹脂成形品に対し、優れ
た密着性を有するプライマー組成物に関する。More specifically, the present invention relates to a primer composition that has excellent adhesion to phenolic resin molded products, which have often been used unpainted due to adhesion problems.
従来技術
従来より、フェノール樹脂素材はその電気特性や耐熱性
に優れていることから、電気製品や自動車内装品として
の灰皿等に使用されてきた。PRIOR ART Conventionally, phenolic resin materials have been used for electrical products and ashtrays as automobile interior parts because of their excellent electrical properties and heat resistance.
塗装の分野においては、メラミンアルキッド塗料に代表
されるメラミン硬化型塗料、アクリルウレタン塗料に代
表されるイソシアネート硬化型塗料および酸化硬化型ア
ルキッド塗料が1コート上塗塗料として使用されてきた
。そのため現状はプライマーを不要としており、また無
塗装で使用されている場合も多いことから、その開発、
改良も行われてこなかった。In the field of coatings, melamine-curing paints such as melamine alkyd paints, isocyanate-curing paints such as acrylic urethane paints, and oxidation-curing alkyd paints have been used as one-coat top paints. Therefore, currently there is no need for a primer, and since it is often used without painting, its development,
No improvements have been made.
近年になって、趣味の多彩化、デザインの多様化から自
動車の内装部品においても各種のデザインの塗料が開発
され、適用されてきている。In recent years, due to the diversification of hobbies and diversification of designs, paints with various designs have been developed and applied to interior parts of automobiles.
しかし、これらの塗料はフェノール樹脂素材に対する密
着性が弱く、その跋までは使用できないため、密着性の
良好なプライマー開発が待たれている。従来技術のメラ
ミンアルキッド塗料等の1コート上塗塗料をプライマー
として利用することも試みられてきたが、このようなプ
ライマー塗膜の上に上塗塗料を塗装すると、やはりフェ
ノール樹脂素材面と塗膜との密着性が低下するため、現
在まで塗装が行われてこなかった。また、ウレタンラッ
カー系塗料はプライマーとして使用した時、密着性は良
好であるが耐湿性試験(50℃×98%RH,10日間
)においてフクロが発生するため、これも性能的に不十
分である。However, these paints have weak adhesion to phenolic resin materials and cannot be used to such an extent that the development of a primer with good adhesion is awaited. Attempts have been made to use conventional one-coat top coat paints such as melamine alkyd paints as primers, but when top coat paints are applied on top of such primer coats, there is still a possibility that the phenolic resin material surface and the paint film will be in contact with each other. Painting has not been done until now because it reduces adhesion. In addition, when urethane lacquer paint is used as a primer, it has good adhesion, but flakes occur during the moisture resistance test (50°C x 98% RH, 10 days), so this is also insufficient in terms of performance. .
発明の解決しようとする問題点
フェノール樹脂成形品の高級仕上げ塗装において、その
塗装仕上げを可能とする密着性に優れたプライマーを開
発し、今後の自動車内装の高級仕上げ化を可能とするプ
ライマーを開発することが本発明の目的である。Problems to be solved by the invention Developed a primer with excellent adhesion that enables high-grade finishing coating of phenolic resin molded products, and developed a primer that will enable high-grade finishing of future automobile interiors. It is an object of the present invention to do so.
問題を解決するための手段
本発明に従えは、上記目的が(A)ウレタンポリオール
に顔料を配合したものを主成分とする主剤成分と(B)
ポリイソシアネートプレポリマーを主成分とする硬化剤
成分とからなるイソシアネート硬化型の2液型フェノー
ル樹脂成形品用プライマー組成物に於いて、ウレタンポ
リオールのOH価が5〜40であり、ウレタンポリオー
ル100(固形分重量)部に対し、ポリイソシアネート
プレポリマーが2〜60(固形分重量)部の割合からな
ることを特徴とするイソシアネート硬化型の2液型フェ
ノール樹脂成形品用プライマー組成物により達成できる
。Means for Solving the Problem According to the present invention, the above-mentioned object is achieved by combining (A) a main component containing a pigment blended with a urethane polyol;
In the isocyanate-curing type two-component primer composition for phenolic resin molded products, which is composed of a curing agent component containing a polyisocyanate prepolymer as a main component, the OH value of the urethane polyol is 5 to 40, and the urethane polyol has a hardening agent component of 100 ( This can be achieved by an isocyanate-curable two-component primer composition for phenolic resin molded articles, which is characterized in that the polyisocyanate prepolymer is contained in a ratio of 2 to 60 parts (solid weight) to 2 parts (solid weight).
本発明の2液型ブライマ一組成物の(A>主剤成分に使
用するウレタンポリオールとしては、主鎖にウレタン結
合を含むポリオールであって例えばポリアルキレングリ
コールや直鎖ポリエステルポリオールとイソホロンジイ
ソシアネート、ヘキサメチレンジイソシアネート、トリ
レンジイソシアネートなどの2官能イソシアネートを反
応させたものなどが好適に使用せられる。The urethane polyol used as the main component (A) of the two-component brimer composition of the present invention is a polyol containing a urethane bond in the main chain, such as polyalkylene glycol, linear polyester polyol, isophorone diisocyanate, hexamethylene Those obtained by reacting bifunctional isocyanates such as diisocyanate and tolylene diisocyanate are preferably used.
また、必要に応じて他のポリオール、例えば主鎖がC−
C結合からなるアクリルポリオール、主鎖にポリエステ
ル結合を含むポリエステルポリオール、主鎖にエーテル
結合を含むポリエーテルポリオール、主鎖にエポキシ官
能基を有するエポキシポリオール、ニトロセルローズ系
樹脂、またはアルキド樹脂等の1種または2種以上をウ
レタンポリオールの10重量%の範囲内であれば併用す
ることも可能である。In addition, other polyols, such as those whose main chain is C-
1 such as acrylic polyol consisting of C bonds, polyester polyol containing polyester bond in the main chain, polyether polyol containing ether bond in the main chain, epoxy polyol having epoxy functional group in the main chain, nitrocellulose resin, or alkyd resin. It is also possible to use one or more types in combination within the range of 10% by weight of the urethane polyol.
これらのウレタンポリオールのOH価は5〜40の範囲
にあることが必要とされる。06価5未満では耐湿性試
験においてフクロが発生し、01価40を超えても同様
にフクロが発生するため好ましくない。The OH value of these urethane polyols is required to be in the range of 5 to 40. If the 06 value is less than 5, flakes will occur in the moisture resistance test, and if the 01 valence exceeds 40, the same flakes will occur, which is not preferable.
本発明の2液型ブライマ一組成物の(B)硬化剤成分の
ポリイソシアネートプレポリマーとしては、通常のイソ
シアネート基を有する化合物あるいはそのプレポリマー
が好都合に使用せられる。As the polyisocyanate prepolymer of the curing agent component (B) in the two-component brimer composition of the present invention, conventional compounds having isocyanate groups or prepolymers thereof are conveniently used.
例えば、無黄変型または難黄変型として知られている脂
肪族もしくは脂環族ジイソシアネート化合物(イソホロ
ンジイソシアネート、水素化ジフェニルメタンジイソシ
アネートなど)、黄変型として知られている芳香族ジイ
ソシアネーI・化合物(ジフェニルメタン−4,4゛−
ジイソシアネートなど)、トリイソシアネート化合物あ
るいはウレア結合、アロファネート結合、ビイウレット
結合、イソシアヌレート環構造を含むポリイソシアネー
ト類、さらに活性水素化合物と反応せしめて得られるイ
ソシアネート基末端プレポリマー(トリレンジイソシア
ネート□トリメチロールプロパン系プレポリマーキシリ
レンジイソシアネート□トリメチロールプロパン系プレ
ポリマーなど)が挙げられ、これらポリイソシアネート
は単独で使用しても2種以上混合して使用してもよい。For example, aliphatic or alicyclic diisocyanate compounds known as non-yellowing type or non-yellowing type (isophorone diisocyanate, hydrogenated diphenylmethane diisocyanate, etc.), aromatic diisocyanate I compounds known as yellowing type (diphenylmethane-4 ,4゛-
diisocyanate, etc.), triisocyanate compounds or polyisocyanates containing urea bonds, allophanate bonds, biuret bonds, isocyanurate ring structures, and isocyanate group-terminated prepolymers obtained by reacting with active hydrogen compounds (tolylene diisocyanate □ trimethylolpropane). xylylene diisocyanate, trimethylolpropane prepolymer, etc.), and these polyisocyanates may be used alone or in combination of two or more.
上記ポリウレタンポリオールとポリイソシアネートプレ
ポリマーの固形分重量比はボリウレタンボリオール10
0部に対し、ポリイソシアネートプレボリマー2〜60
部の範囲内にあることが必要とされる。ポリイソシアネ
ートプレポリマーが2部未満では耐湿試験でフクレが発
生し、60部を超えると塗膜に粘着性がでるほか耐湿試
験で密着性が不十分となるため好ましくない
ウレタンポリオールに配合される顔料としては通常塗料
に使用されている着色顔料および体質顔料か殆どすべて
使用できる。The solid content weight ratio of the above polyurethane polyol and polyisocyanate prepolymer is polyurethane polyol 10
0 parts to 2 to 60 parts of polyisocyanate prebolimer
must be within the range of If the amount of polyisocyanate prepolymer is less than 2 parts, blistering will occur in the moisture resistance test, and if it exceeds 60 parts, the coating will become sticky and the adhesion will be insufficient in the moisture resistance test, which is undesirable. Pigment blended with urethane polyol Almost all color pigments and extender pigments commonly used in paints can be used.
代表的なものとしては、例えば着色顔料としては、二酸
化チタン、弁柄、カーボンブラック、フタロシアニンブ
ルー、キナクリドンレッド系レッド、フタロシアニング
リーン等が挙げられる。体質顔料としては、沈降性硫酸
バリウム、タルク、炭酸カルシウム等が挙げられる。溶
剤としてはアルコール系溶剤はイソシアネートと反応す
るため好ましくないが、それ以外の有機溶剤は殆ど使用
可能であり、塗装環境に応じて適宜配合して使用される
。Typical examples of color pigments include titanium dioxide, Bengara, carbon black, phthalocyanine blue, quinacridone red, phthalocyanine green, and the like. Extender pigments include precipitated barium sulfate, talc, calcium carbonate, and the like. Alcohol solvents are not preferred as they react with isocyanate, but most other organic solvents can be used, and are mixed as appropriate depending on the coating environment.
この他、必要に応じ各種の添加剤が使用できる。添加剤
としては、例えばジメチルポリシロキサンに代表される
シリコン系添加剤、脂肪酸アマイド、ポリアルキレング
リコール等が挙げられる。もちろん、反応触媒として、
ジブチル錫ジラウレートやナフテン酸コバルトに代表さ
れる2液量塗料用反応促進剤も適宜使用できる。In addition, various additives can be used as necessary. Examples of additives include silicone additives typified by dimethylpolysiloxane, fatty acid amides, polyalkylene glycols, and the like. Of course, as a reaction catalyst,
Reaction accelerators for two-component paints, such as dibutyltin dilaurate and cobalt naphthenate, can also be used as appropriate.
ウレタンポリオールに配合される上記の着色顔料、体質
顔料等は必要によりその他の成分、すなわち溶剤、添加
剤等と共にウレタンポリオール中に混合し、分散機を用
いて均一に分散され(A)主剤成分塗料液として調製さ
れる。The above-mentioned coloring pigments, extender pigments, etc. that are blended into the urethane polyol are mixed into the urethane polyol together with other components, such as solvents and additives, if necessary, and are uniformly dispersed using a dispersing machine to form (A) main component paint. Prepared as a liquid.
この様にして調製された(A)主剤成分塗料液と(B)
硬化剤成分の硬化剤とは2液型塗料であるので、塗装に
際して混合され、本発明によるプライマー塗料液として
調製され、スプレー方式等により塗装できる。(A) base component coating liquid prepared in this manner and (B)
Since the curing agent of the curing agent component is a two-component paint, it is mixed at the time of painting to prepare a primer paint liquid according to the present invention, which can be applied by a spray method or the like.
効 果
本発明によるプライマーは、従来のフェノール樹脂成形
品用塗料と異なり、各種の上塗塗料の適用が可能であり
、本発明のプライマー開発によって従来不可能であった
フェノール樹脂成形品の加飾を可能とし、塗料で可能な
新規意匠の適用を可能としたことが挙げられる。すなわ
ちデザインの自由度を大幅に拡げたことが大きな効果と
して挙げられる。Effects Unlike conventional paints for phenolic resin molded products, the primer according to the present invention can be applied with various top coats, and the development of the primer of the present invention has made it possible to decorate phenolic resin molded products, which was previously impossible. This is because it has made it possible to apply new designs that are possible with paint. In other words, a major effect is that the degree of freedom in design has been greatly expanded.
実施例
次に実施例および比較例によって本発明をさらに詳細に
説明する。各鋼中、部は重量部を示す。EXAMPLES Next, the present invention will be explained in more detail with reference to Examples and Comparative Examples. In each steel, parts indicate parts by weight.
実施例1〜5、比較例1〜4
70Il111 X 701m X 3+aの市販フェ
ノール樹脂板の表面をイソプロピルアルコール含浸布で
拭き、その汚れを除去した後、塗装粘度(7オートカツ
プNO,4゜20°Cにて13秒)に希釈シンナーで調
整したプライマーを空気霧化塗装し、次いで80’Cに
て30分間加熱乾燥した(乾燥膜要約10μ)0次いで
市販上塗塗料(日本ビーケミカル株式会社製、商品名:
R−263)を同上塗塗料専用シンナーにて、塗装粘度
(フォーFカフフN0.4.20℃にて14秒)に調整
して、前記プライマー塗膜上に空気霧化塗装した後、8
0℃にて30分間加熱乾燥したく乾燥膜厚はプライマー
、上塗塗料の合計で40μ)。Examples 1 to 5, Comparative Examples 1 to 4 After wiping the surface of a commercially available phenol resin plate measuring 70Il111 x 701m x 3+a with an isopropyl alcohol-impregnated cloth to remove the stain, the coating viscosity (7 Auto Cup NO., 4°20°C A primer prepared with diluted thinner was applied by air atomization (13 seconds at given name:
R-263) was adjusted to a coating viscosity (Four F Cuff N0.4, 14 seconds at 20°C) using the same topcoat paint thinner, and air atomization was applied on the primer coating.
Dry by heating at 0°C for 30 minutes (dry film thickness is 40μ in total of primer and top coat).
第1表には使用したプライマー各成分の種類と組成およ
び希釈シンナーの配合成分の種類と組成等を示した。Table 1 shows the type and composition of each component of the primer used and the type and composition of the diluting thinner components.
得られた試験片について、耐湿試験ならびに同試験前後
の塗膜の密着試験を実施し、それらの結果を第1表に併
記した。The obtained test pieces were subjected to a moisture resistance test and a coating film adhesion test before and after the test, and the results are also listed in Table 1.
次に試験方法を示す。The test method is shown below.
耐湿性;
温度49±1℃、相対湿度98%のヒューミディテイ・
キャビネット中に試験片を入れ、240時間放置後取り
出し、フクレ発生の有無を評価した。Humidity resistance; temperature 49±1℃, relative humidity 98%
A test piece was placed in a cabinet, left for 240 hours, and then taken out to evaluate the presence or absence of blistering.
評価基準;フクレなき場合はO、フクレ発生の場合は×
とした。Evaluation criteria: O if there is no blistering, × if blistering occurs
And so.
m二
試験片の塗膜面にカッターナイフで縦横に2態動間隔で
、素材に達する11本の線を引き、できた100個のマ
ス目にセロハンテープを密着させ、−気にはがした時の
剥離の状態により評価した。11 lines reaching the material were drawn on the coated surface of the m2 test piece with a cutter knife at 2-position intervals vertically and horizontally, cellophane tape was applied to the 100 squares created, and then carefully peeled off. Evaluation was made based on the state of peeling.
評価基準:剥離なき場合は○、全面剥離の場合は×とし
た。Evaluation criteria: ○ if there was no peeling, and × if the entire surface peeled.
Claims (1)
分とする主剤成分と(B)ポリイソシアネートプレポリ
マーを主成分とする硬化剤成分とからなるイソシアネー
ト硬化型の2液型フェノール樹脂成形品用プライマー組
成物に於いて、ウレタンポリオールのOH価が5〜40
であり、ウレタンポリオール100(固形分重量)部に
対し、ポリイソシアネートプレポリマーが2〜60(固
形分重量)部の割合からなることを特徴とするイソシア
ネート硬化型の2液型フェノール樹脂成形品用プライマ
ー組成物。An isocyanate-curing type two-component primer for phenolic resin molded products, consisting of (A) a main component whose main component is a mixture of urethane polyol and a pigment, and (B) a curing agent component whose main component is a polyisocyanate prepolymer. In the composition, the OH value of the urethane polyol is 5 to 40.
For use in isocyanate-curable two-component phenolic resin molded products, characterized in that the polyisocyanate prepolymer is comprised of 2 to 60 parts (solid weight) of polyisocyanate prepolymer to 100 parts (solid weight) of urethane polyol. Primer composition.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP9074090A JPH03287679A (en) | 1990-04-04 | 1990-04-04 | Primer composition for phenolic resin |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP9074090A JPH03287679A (en) | 1990-04-04 | 1990-04-04 | Primer composition for phenolic resin |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH03287679A true JPH03287679A (en) | 1991-12-18 |
Family
ID=14006979
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP9074090A Pending JPH03287679A (en) | 1990-04-04 | 1990-04-04 | Primer composition for phenolic resin |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH03287679A (en) |
-
1990
- 1990-04-04 JP JP9074090A patent/JPH03287679A/en active Pending
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