JPS62230868A - Coating composition for chipping resistance - Google Patents
Coating composition for chipping resistanceInfo
- Publication number
- JPS62230868A JPS62230868A JP7344086A JP7344086A JPS62230868A JP S62230868 A JPS62230868 A JP S62230868A JP 7344086 A JP7344086 A JP 7344086A JP 7344086 A JP7344086 A JP 7344086A JP S62230868 A JPS62230868 A JP S62230868A
- Authority
- JP
- Japan
- Prior art keywords
- parts
- chipping
- coating composition
- filler
- weight
- 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
- 239000008199 coating composition Substances 0.000 title claims description 28
- 239000000945 filler Substances 0.000 claims abstract description 24
- 239000012765 fibrous filler Substances 0.000 claims abstract description 13
- 239000004925 Acrylic resin Substances 0.000 claims abstract description 12
- 229920000178 Acrylic resin Polymers 0.000 claims abstract description 12
- 239000007787 solid Substances 0.000 claims abstract description 8
- 239000000843 powder Substances 0.000 claims description 10
- 229910052751 metal Inorganic materials 0.000 claims description 9
- 239000002184 metal Substances 0.000 claims description 9
- 239000000835 fiber Substances 0.000 claims description 4
- 239000011248 coating agent Substances 0.000 abstract description 15
- 238000000576 coating method Methods 0.000 abstract description 15
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 abstract description 14
- 229910000019 calcium carbonate Inorganic materials 0.000 abstract description 7
- 239000000203 mixture Substances 0.000 abstract description 5
- 239000000454 talc Substances 0.000 abstract description 3
- 229910052623 talc Inorganic materials 0.000 abstract description 3
- 229920000049 Carbon (fiber) Polymers 0.000 abstract description 2
- 239000004917 carbon fiber Substances 0.000 abstract description 2
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 abstract description 2
- 239000002245 particle Substances 0.000 abstract description 2
- 238000002156 mixing Methods 0.000 abstract 1
- 239000010408 film Substances 0.000 description 23
- 230000008961 swelling Effects 0.000 description 17
- 230000000052 comparative effect Effects 0.000 description 9
- 238000001035 drying Methods 0.000 description 8
- 150000002681 magnesium compounds Chemical class 0.000 description 8
- 239000000047 product Substances 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 4
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 4
- 239000000178 monomer Substances 0.000 description 4
- 239000011347 resin Substances 0.000 description 4
- 229920005989 resin Polymers 0.000 description 4
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- -1 alkylstyrene Chemical compound 0.000 description 3
- 230000007423 decrease Effects 0.000 description 3
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 3
- 229920000126 latex Polymers 0.000 description 3
- 239000004816 latex Substances 0.000 description 3
- LQBJWKCYZGMFEV-UHFFFAOYSA-N lead tin Chemical compound [Sn].[Pb] LQBJWKCYZGMFEV-UHFFFAOYSA-N 0.000 description 3
- 239000010409 thin film Substances 0.000 description 3
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- 229910001128 Sn alloy Inorganic materials 0.000 description 2
- 229910000831 Steel Inorganic materials 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- 239000006229 carbon black Substances 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 239000002270 dispersing agent Substances 0.000 description 2
- 229920001971 elastomer Polymers 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 2
- 239000010931 gold Substances 0.000 description 2
- 229910052737 gold Inorganic materials 0.000 description 2
- 229920001519 homopolymer Polymers 0.000 description 2
- 238000010422 painting Methods 0.000 description 2
- 239000000049 pigment Substances 0.000 description 2
- 238000007747 plating Methods 0.000 description 2
- 230000003449 preventive effect Effects 0.000 description 2
- 239000010959 steel Substances 0.000 description 2
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- POAOYUHQDCAZBD-UHFFFAOYSA-N 2-butoxyethanol Chemical compound CCCCOCCO POAOYUHQDCAZBD-UHFFFAOYSA-N 0.000 description 1
- CFVWNXQPGQOHRJ-UHFFFAOYSA-N 2-methylpropyl prop-2-enoate Chemical compound CC(C)COC(=O)C=C CFVWNXQPGQOHRJ-UHFFFAOYSA-N 0.000 description 1
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 1
- 239000005909 Kieselgur Substances 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- GYCMBHHDWRMZGG-UHFFFAOYSA-N Methylacrylonitrile Chemical compound CC(=C)C#N GYCMBHHDWRMZGG-UHFFFAOYSA-N 0.000 description 1
- CNCOEDDPFOAUMB-UHFFFAOYSA-N N-Methylolacrylamide Chemical compound OCNC(=O)C=C CNCOEDDPFOAUMB-UHFFFAOYSA-N 0.000 description 1
- 229920000459 Nitrile rubber Polymers 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 125000002723 alicyclic group Chemical group 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 239000010425 asbestos Substances 0.000 description 1
- 229960000892 attapulgite Drugs 0.000 description 1
- QBLDFAIABQKINO-UHFFFAOYSA-N barium borate Chemical compound [Ba+2].[O-]B=O.[O-]B=O QBLDFAIABQKINO-UHFFFAOYSA-N 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 229920005549 butyl rubber Polymers 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- ZCDOYSPFYFSLEW-UHFFFAOYSA-N chromate(2-) Chemical class [O-][Cr]([O-])(=O)=O ZCDOYSPFYFSLEW-UHFFFAOYSA-N 0.000 description 1
- 229920006026 co-polymeric resin Polymers 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 230000001010 compromised effect Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 239000012043 crude product Substances 0.000 description 1
- NJLLQSBAHIKGKF-UHFFFAOYSA-N dipotassium dioxido(oxo)titanium Chemical compound [K+].[K+].[O-][Ti]([O-])=O NJLLQSBAHIKGKF-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000007720 emulsion polymerization reaction Methods 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 229910002804 graphite Inorganic materials 0.000 description 1
- 239000010439 graphite Substances 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 1
- 235000019341 magnesium sulphate Nutrition 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 229910001463 metal phosphate Inorganic materials 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 239000010445 mica Substances 0.000 description 1
- 229910052618 mica group Inorganic materials 0.000 description 1
- 239000011490 mineral wool Substances 0.000 description 1
- 239000012860 organic pigment Substances 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 229910052625 palygorskite Inorganic materials 0.000 description 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- LYBIZMNPXTXVMV-UHFFFAOYSA-N propan-2-yl prop-2-enoate Chemical compound CC(C)OC(=O)C=C LYBIZMNPXTXVMV-UHFFFAOYSA-N 0.000 description 1
- 239000011241 protective layer Substances 0.000 description 1
- 229910052895 riebeckite Inorganic materials 0.000 description 1
- 230000000630 rising effect Effects 0.000 description 1
- 239000005060 rubber Substances 0.000 description 1
- 238000007665 sagging Methods 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
Landscapes
- Paints Or Removers (AREA)
Abstract
Description
【発明の詳細な説明】
[産業上の利用分野]
本発明は金属製品表面に被覆され、その金属製品をチッ
ピングから保護するための耐チッピング用被覆組成物に
関する。本発明の耐チッピング用被′11組成物は例え
ば自動車のガソリンタンク表面被覆用などに利用される
。DETAILED DESCRIPTION OF THE INVENTION [Industrial Application Field] The present invention relates to a chipping-resistant coating composition that is coated on the surface of a metal product to protect the metal product from chipping. The chipping-resistant coating '11 composition of the present invention is used, for example, to coat the surface of an automobile gasoline tank.
[従来の技術l
鉛−錫合金メッキが施された鋼材は、ターンシートと呼
ばれ伸展性に富んでいる。従って板金加工性を儂ねるこ
とがないので、従来自動車のガソリンタンクなどに多用
されている。この鉛−錫合金メッキは極めて優れた防錆
力を有している。しかしながら傷などによりメッキ面に
損傷が生じlζ場合にはその部位から腐蝕が進行する。[Prior Art I] A steel material plated with a lead-tin alloy is called a turn sheet and is highly extensible. Therefore, since sheet metal workability is not compromised, it has been widely used for automobile gasoline tanks and the like. This lead-tin alloy plating has extremely excellent anti-rust properties. However, if the plated surface is damaged due to scratches or the like, corrosion will progress from that area.
従つ゛にのにうなメッキ面の傷付きを防止するために、
従来メッキ面を保護する保Ale Uとして耐チッピン
グ用被覆組成物で被覆されている。To prevent scratches on the plating surface,
Conventionally, the plated surface is coated with a chipping-resistant coating composition as a protective layer.
この従来の耐チッピング用被覆組成物は、特開昭58−
187469号公報にも見られるように、一般に水分散
性アクリル樹脂をバインダーとして用い、タルク、炭酸
カルシウムなどの粉質充填剤が配合された塗料が用いら
れている。そしてエアレス塗装などにより300μ〜8
00μという厚膜に塗装され、乾燥して被覆されている
。This conventional chipping-resistant coating composition is
As seen in Japanese Patent Application No. 187469, paints are generally used in which a water-dispersible acrylic resin is used as a binder and powdered fillers such as talc and calcium carbonate are mixed therein. And 300μ~8 by airless painting etc.
It is coated with a thick film of 00μ, dried and coated.
[発明が解決しようとする問題点]
上記した従来の耐チッピング用被覆組成物においては、
塗布膜厚を300μ〜800μと厚くしないと良好な耐
チッピング性が得られないという不具合がある。そのた
めに作業性が悪く、被覆組成物の昂も多く必要であり、
コストの上昇を沼いていた。[Problems to be Solved by the Invention] In the conventional chipping-resistant coating composition described above,
There is a problem that good chipping resistance cannot be obtained unless the coating film thickness is increased to 300 μm to 800 μm. As a result, workability is poor and a large amount of coating composition is required.
They were worried about rising costs.
耐デツピング性を向上させるには粉質充填剤の配合量を
減らす方法が考えられる。即ち、水分散性アクリル樹脂
の配合量を相対的に多くし、強度をもたせればよい。し
かしながら従来耐チッピング用被覆組成物はガソリンタ
ンクなどに塗布された後80℃〜120℃の高温で乾燥
されている。One possible method for improving the depping resistance is to reduce the amount of powder filler blended. That is, the amount of water-dispersible acrylic resin blended may be relatively increased to provide strength. However, conventional anti-chipping coating compositions have been applied to gasoline tanks and the like and then dried at high temperatures of 80°C to 120°C.
従って上記のように樹脂成分のが多い場合には造膜が早
期に行われるため表面乾燥が早く、乾燥時の熱により蒸
発した水蒸気がその樹脂膜を押圧することにより塗膜に
脹れが生じるような不具合があった。Therefore, when there is a large amount of resin component as mentioned above, film formation occurs early and the surface dries quickly, and the water vapor evaporated by the heat during drying presses the resin film, causing swelling in the coating film. There was a problem like this.
即ち、粉質充填剤が少ない場合には耐チッピング性は向
上するが脹れが生じる。一方粉質充填剤が多い場合には
、蒸気となった水は容易に塗膜中から外部へ扱けて脹れ
は生じないが、膜厚を厚くしないと耐チッピング性に劣
るという不具合がある。That is, when the amount of powdery filler is small, chipping resistance is improved, but swelling occurs. On the other hand, if there is a large amount of powder filler, water that becomes steam can be easily handled from the inside of the coating film to the outside and no swelling will occur, but if the film thickness is not thick, the chipping resistance will be poor. .
本発明は上記問題点に鑑みてなされたものであり、乾燥
時の脹れの発生を抑制し、かつ薄膜でも耐デツピング性
に優れた耐チッピング用被覆組成物を提供することを目
的とする。The present invention has been made in view of the above problems, and an object of the present invention is to provide a chipping-resistant coating composition that suppresses the occurrence of swelling during drying and has excellent depping resistance even in a thin film.
[問題点を解決jるための手段]
本発明の耐チッピング用被覆組成物は、水分散性アクリ
ル樹脂が固形分で100重量部と、粉質充填剤10〜6
0重量部と、m雄状充填剤10〜60重量部00重市な
り、金属製品表面に被覆されて該金属製品をチッピング
から保護することを特徴とする。[Means for solving the problems] The chipping-resistant coating composition of the present invention contains 100 parts by weight of a water-dispersible acrylic resin as a solid content, and 10 to 6 parts by weight of a powdery filler.
0 parts by weight of the male filler and 10 to 60 parts by weight of the male filler, which is coated on the surface of a metal product to protect the metal product from chipping.
本発明に用いられる水分散性アクリル樹脂は、各種ビニ
ルモノマーを乳化重合法にて重合したものをいい、その
七ツマ−の種類としては例えばスチレン、アルキルスチ
レン、アクリル酸もしくはメタアクリル酸アルキル、ア
クリロニトリル、アクリルアマイド、N−メチロールア
クリルアマイド、メタアクリルニトリル、アクリル酸ま
たはメタアクリル酸の脂環もしくは芳香環を有する炭化
水素エステル類などが用いられ、その単独重合体あるい
は共重合体樹脂を用いることができる。The water-dispersible acrylic resin used in the present invention is one obtained by polymerizing various vinyl monomers by emulsion polymerization, and examples of the seven monomers include styrene, alkylstyrene, alkyl acrylic acid or methacrylate, and acrylonitrile. , acrylamide, N-methylol acrylamide, methacrylonitrile, hydrocarbon esters having an alicyclic or aromatic ring of acrylic acid or methacrylic acid, etc., and their homopolymers or copolymer resins can be used. can.
好ましいモノマーの組合わせとしては、例えばアクリル
酸エチル、アクリル酸イソプロピル、アクリルflJ−
n−プロピル、アクリル酸イソブチル、アクリル酸−n
−ブチル、アクリルl!!−2−エチルヘキシルなどの
モノマーの単独m合体もしくは共重合体などを例示する
ことができる。Preferred monomer combinations include, for example, ethyl acrylate, isopropyl acrylate, and acrylic flJ-
n-propyl, isobutyl acrylate, n-acrylate
-Butyl, acrylic! ! Examples include homopolymers or copolymers of monomers such as -2-ethylhexyl.
本発明の耐チッピング用被覆組成物には所望に応じて他
の水分散性樹脂、例えばスチレン−ブタジェンゴムラテ
ックス、ニトリル−ブタジェンゴムラテックス、ブチル
ゴムラテックス、酢酸ビニルエマルジョン、酢酸ビニル
共重合エマルジョン、ポリウレタン水分数体などの樹脂
を上記水分散性アクリル樹脂に混合して用いることもで
きる。The chipping-resistant coating composition of the present invention may optionally contain other water-dispersible resins, such as styrene-butadiene rubber latex, nitrile-butadiene rubber latex, butyl rubber latex, vinyl acetate emulsion, vinyl acetate copolymer emulsion, It is also possible to use a resin such as a polyurethane water compound mixed with the water-dispersible acrylic resin.
本発明にいう粉質充填剤は、従来用いられているものと
同様のものを用いることができ、例えば、タルク、炭酸
カルシウム、珪藻土、マイカ、力Aリン、硫酸バリウム
、グラファイト、アルミナ、酸化鉄、酸化チタン、シリ
カ、ゴム粉末、ガラスフレークなどを1種もしくは2梗
以上混合して用いることができる。The powder filler referred to in the present invention can be the same as those conventionally used, such as talc, calcium carbonate, diatomaceous earth, mica, phosphoric acid, barium sulfate, graphite, alumina, iron oxide. , titanium oxide, silica, rubber powder, glass flakes, etc., may be used alone or in combination of two or more.
この粉質充填剤の形状は特に制限されないが、粒径が大
きくなり過ぎると、塗装時につまりが生じたり、被覆後
の表面に凹凸が生じる場合があるので、1〜50μの粒
子径を有するものが好ましい。The shape of this powder filler is not particularly limited, but if the particle size becomes too large, clogging may occur during coating or unevenness may occur on the surface after coating. is preferred.
上記粉質充填剤は水’t>散性アクリル樹脂固形分10
0重量部に対して10〜60重吊部の割合で用いる。配
合化が10手開部以下の場合には乾燥時に脹れが生じ、
60重は部より多くなると耐チッピング性が低下する。The above powder filler is water't>dispersible acrylic resin solid content 10
It is used at a ratio of 10 to 60 parts by weight to 0 parts by weight. If the formulation is less than 10 times, swelling will occur during drying,
When the weight exceeds 60 parts, the chipping resistance decreases.
本発明にいう繊維状充填剤は、m維形状をなしていれば
特に制限されず、例えばカーボンファイバー、ロックウ
ール、繊維状チタン酸カリウム、繊維状硫酸マグネシウ
ム、アタパルジャイト、つAラストナイト、Ill状状
硫酸バリウムアスベストなどを用いることができる。The fibrous filler referred to in the present invention is not particularly limited as long as it has an m-fiber shape, and examples thereof include carbon fiber, rock wool, fibrous potassium titanate, fibrous magnesium sulfate, attapulgite, A-lastonite, and Ill-like filler. Barium sulfate asbestos or the like can be used.
このmN状充填剤は、前記水分散性アクリル樹脂固形分
100重量部に対して10〜100重最部とな重量うに
配合覆る。この繊維状充填剤が10重酊部より少ないと
乾燥時に脹れが生じる場合があり、100ffiff1
部より多く配合すると耐チッピング性が低下し塗膜外観
形状も悪くなる。The mN filler is mixed in an amount of 10 to 100 parts by weight based on 100 parts by weight of the solid content of the water-dispersible acrylic resin. If the amount of this fibrous filler is less than 10 parts, swelling may occur during drying.
If more than 10% is added, the chipping resistance will decrease and the appearance of the coating will also deteriorate.
この繊維状充填剤の単繊維の形状は特に制限はされない
が、長さが10〜200μmおよび断面の最大径が0.
1〜3μmであることが望ましい。The shape of the single fibers of this fibrous filler is not particularly limited, but the length is 10 to 200 μm and the maximum diameter of the cross section is 0.5 μm.
The thickness is preferably 1 to 3 μm.
断面の径および良さがこの範囲にあれば、乾燥時の脹れ
の防止、耐チッピング性および塗膜の表面外観を特に良
好に維持することができる。また特にはアスペクト比が
50〜200のものを用いることが好ましい。アスベク
!・比がこの範囲にあれば上記性能を特に高く維持する
ことができる。If the cross-sectional diameter and quality are within this range, prevention of swelling during drying, chipping resistance, and surface appearance of the coating film can be maintained particularly well. In particular, it is preferable to use one having an aspect ratio of 50 to 200. Asbek! - If the ratio is within this range, the above performance can be maintained particularly high.
粉質充填剤と繊維状充填剤の総量は、水分散性アクリル
樹脂の固形分100重量部に対し50〜160重聞部と
16のが望ましい。この総量が70重量部より少ないと
脹れが生じやすく、160fflffi部より多いと薄
膜時に耐チッピング性が低下するようになる。The total amount of the powder filler and the fibrous filler is desirably 50 to 160 parts by weight, or 16 parts by weight, based on 100 parts by weight of the solid content of the water-dispersible acrylic resin. If the total amount is less than 70 parts by weight, swelling tends to occur, and if it is more than 160 parts by weight, the chipping resistance will decrease when forming a thin film.
本発明の耐チッピング用被覆組成物には、上記配合物以
外にカーボンブラック、有機顔料などの着色顔料、クロ
ム酸金属塩、リン酸金属塩、メタホウ酸金属塩などの防
錆顔料、分散剤、増粘剤などの添加剤およびエチレング
リコール、ブチルセロソルブなどの有機溶剤などを混合
することもできる。In addition to the above ingredients, the chipping-resistant coating composition of the present invention includes carbon black, color pigments such as organic pigments, rust preventive pigments such as metal chromates, metal phosphates, and metal metaborates, dispersants, Additives such as thickeners and organic solvents such as ethylene glycol and butyl cellosolve can also be mixed.
本発明の耐チッピング用被覆組成物を金DM品表面に被
覆するには、エアレス塗装、エアスプレー塗装などを用
いて金m製品表面に塗布する。その後例えば80℃〜1
20℃の温度で10分〜30分乾燥し硬化させることに
より被膜を1!する。なお本発明の耐チッピング用被覆
組成物を用いれば従来はど厚膜にする必要なく、70μ
〜200μ程度の薄膜でも十分な耐チッピング性を有す
る。In order to coat the surface of the gold DM product with the chipping-resistant coating composition of the present invention, it is applied to the surface of the gold DM product using airless coating, air spray coating, or the like. After that, for example, 80℃~1
The film is cured by drying for 10 to 30 minutes at a temperature of 20°C. do. In addition, if the chipping-resistant coating composition of the present invention is used, there is no need to make a film as thick as 70 μm.
Even a thin film of ~200μ has sufficient chipping resistance.
又従来と同様に300部以上の厚膜とすることもできる
。Further, as in the conventional case, the film can be made thicker than 300 parts.
[作用]
本発明の耐チッピング用被覆組成物は、充填剤として粉
質充填剤および1111状充填剤が配合されている。こ
こで繊維状充填剤は塗膜中に層状に近く配向し、粉質充
填剤とともに略最密充填状態となる。従って充填剤の配
合合計量を従来より多くしても従来と同様の耐チッピン
グ性を得ることができる。また充填剤が多くなることに
より脹れの発生が防止される。故に配合合計量を従来と
略同等量としても、同等の耐チッピング性を有しつつ膜
厚を薄(することができ、かつ脹れは同等以上に防止さ
れる。従って被覆組成物の使用(3)および塗装回数を
低減することができ、コストの低減を図ることができる
。ざらに繊維状充填剤は粉質充填剤の間で層状に近く配
向した状態となるため、小石などの衝撃力を分散させ耐
チッピング性が一層向上する。[Function] The chipping-resistant coating composition of the present invention contains a powdery filler and a 1111-type filler as fillers. Here, the fibrous filler is oriented in a nearly layered manner in the coating film, and together with the powder filler, it is in a nearly close-packed state. Therefore, even if the total amount of fillers blended is larger than the conventional one, the same chipping resistance as the conventional one can be obtained. In addition, the increase in the amount of filler prevents the occurrence of swelling. Therefore, even if the total amount of the coating composition is approximately the same as the conventional one, the film thickness can be made thinner while maintaining the same chipping resistance, and the swelling can be prevented to the same or greater extent. 3) It is possible to reduce the number of times of painting, and it is possible to reduce costs.Since the rough fibrous filler is oriented in a layered manner between the powder fillers, it is possible to reduce the impact force of pebbles etc. is dispersed, further improving chipping resistance.
[実施例]
以下実施例により具体的に説明する。なお以下にいう部
はすべて重量部を意味する。[Example] The following is a concrete explanation using Examples. In addition, all parts mentioned below mean parts by weight.
ゴム社製、固形分55%)180部、分散剤として、ボ
イズ530(花王社製)5部、防錆剤としてメタホウ酸
バリウム10部、および水70部を加えディスパーにて
撹拌しながらI−)tMカルシウム60部、カーボンブ
ラック1部、および繊維状充填剤としての繊維状マグネ
シウム化合物(MOS、宇部興産社製、直径1μm1長
さ10〜100μm)10部を徐々に加え、十分に1党
拌して実施例1の耐チッピング用被覆組成物を得た。180 parts (manufactured by Rubber Co., Ltd., solid content 55%), 5 parts of Boyz 530 (manufactured by Kao Corporation) as a dispersant, 10 parts of barium metaborate as a rust preventive agent, and 70 parts of water were added, and while stirring with a disper, I- ) 60 parts of tM calcium, 1 part of carbon black, and 10 parts of a fibrous magnesium compound (MOS, manufactured by Ube Industries, Ltd., diameter 1 μm, length 10 to 100 μm) as a fibrous filler were gradually added, and the mixture was thoroughly stirred. Thus, the chipping-resistant coating composition of Example 1 was obtained.
(2)塗板作成条件
鋼板に鉛−錫メッキが施されたターンシード板を用意し
、上記で得られた被覆組成物をエアレス塗装し、室温で
10分間セツティングをおいた後so’cxio分+1
20℃X20分の条件テ焼付乾燥した。なお膜厚として
は100μおよび200μの2秤類を作成した。また膜
厚を厚く塗装した場合の乾燥時の脹れの生じ具合を調べ
たが、本実施例の被覆組成物では500μ塗装した場合
にしほとんど脹れは生じなかった。(2) Conditions for making coated plates Prepare a turn-seed plate made of lead-tin plated steel plate, apply the coating composition obtained above in an airless manner, let it set for 10 minutes at room temperature, and then apply so'cxio. +1
It was baked and dried under the conditions of 20° C. for 20 minutes. Two scales were prepared with film thicknesses of 100μ and 200μ. The extent to which swelling occurred during drying when the film was coated with a large thickness was also investigated, and with the coating composition of this example, almost no swelling occurred when the coating was coated with a thickness of 500 μm.
(3)耐チッピング性試験
」二記により得られた100μおよび200μの膜厚を
有する2種類の塗板につき、耐チッピング試験を施して
耐チッピング性能を測定した。なお試験方法としては、
塗板の塗膜表面に対して60度の角度でナツト(M−6
)を2mの高さから連続して落下させ、素地が露出した
ときの落下したナツトのaSωで評価した。結果は表に
示す。(3) Chipping resistance test" Two types of coated plates having film thicknesses of 100μ and 200μ obtained in Section 2 were subjected to a chipping resistance test to measure chipping resistance performance. The test method is as follows:
At an angle of 60 degrees to the coating surface of the coating plate (M-6
) was continuously dropped from a height of 2 m, and the aSω of the fallen nut when the substrate was exposed was evaluated. The results are shown in the table.
(実施例2)
繊維状マグネシウム化合物を100部配合したこと以外
は実施例1と同様にして耐チッピング用被覆組成物を調
整し、同様に塗板を作成し耐チッピング性試験を行った
。結果を表に示す。なお本実施例の場合には800μ以
上の17膜に塗装した場合にも焼付時に脹れは全く生じ
なかった。(Example 2) A chipping-resistant coating composition was prepared in the same manner as in Example 1 except that 100 parts of a fibrous magnesium compound was blended, and a coated plate was similarly prepared and a chipping resistance test was conducted. The results are shown in the table. In the case of this example, no swelling occurred during baking even when 17 films of 800 μm or more were coated.
(実施例3)
炭酸カルシウムを10部および繊維状マグネシウム化合
物を100部としたこと以外は実施例1と同様にして被
覆組成物を調整し、同様に塗板を作成し耐チッピング性
試験を行った。結果を表に示す。なお本実施例の場合も
実施例2と同様に800μ以上の厚膜に塗装した場合に
も脹れは全く生じなかった。(Example 3) A coating composition was prepared in the same manner as in Example 1 except that calcium carbonate was changed to 10 parts and the fibrous magnesium compound was changed to 100 parts, and a coated plate was similarly prepared and a chipping resistance test was conducted. . The results are shown in the table. In this example, as in Example 2, no swelling occurred even when a thick film of 800 μm or more was coated.
(比較例1)
m雄状マグネシウム化合物を配合しないこと以外は実施
例1と同様にして被il粗成物を調整し、同様に塗板を
作成し耐デツピング性試験を行った。(Comparative Example 1) An irradiated crude product was prepared in the same manner as in Example 1 except that the m-male magnesium compound was not blended, and a coated plate was prepared in the same manner and a depping resistance test was conducted.
結果を表に示す。なおこの比較例1の場合には膜厚が1
80μを超えると脹れが発生した。The results are shown in the table. In the case of Comparative Example 1, the film thickness was 1
When it exceeded 80μ, swelling occurred.
(比較例2)
炭酸カルシウムを70部とし、繊維状マグネシウム化合
物を配合しないこと以外は実施例1と同様にして被覆組
成物を調整し、同様に塗板を作成して耐チッピング性試
験を行った。結果を表に示す。(Comparative Example 2) A coating composition was prepared in the same manner as in Example 1 except that 70 parts of calcium carbonate and no fibrous magnesium compound were added, and a coated plate was prepared in the same manner and a chipping resistance test was conducted. . The results are shown in the table.
この比較例2の被覆組成物の場合は炭酸カルシウムが1
0部だけ比較例1よりも多くなっているが、膜厚が80
0μであっても脹れはほとんど生じなかった。In the case of the coating composition of Comparative Example 2, calcium carbonate was 1
The film thickness is 80 parts, but the film thickness is 80 parts more than Comparative Example 1.
Even at 0μ, almost no swelling occurred.
(比較例3)
炭酸カルシウムを120部およびmm状マグネシウム化
合物を配合しないこと以外は実施例1と同様にして被覆
組成物を調整し、同様に塗板を作成して耐チッピング性
試験を行った。結果を表に示す。なおこの比較例3の被
覆組成物では膜厚が800μ以上となっても脹れはほと
んど生じなかった。(Comparative Example 3) A coating composition was prepared in the same manner as in Example 1, except that 120 parts of calcium carbonate and no mm-shaped magnesium compound were blended, and a coated plate was similarly prepared and a chipping resistance test was conducted. The results are shown in the table. In addition, with the coating composition of Comparative Example 3, almost no swelling occurred even when the film thickness was 800 μm or more.
(評価)
表より明らかに!1lIi状マグネシウム化合物が配合
された実施例の被覆組成物は、膜厚が厚くなっても乾燥
時に服れツメ生じず比較例に比べてはるかにすぐれてい
る。一方耐チッピング性は1IIJfが100μ、20
0μと薄くとも、2.5〜3.5に9の値を示し、比較
例に比べて同等以上の性能を有している。この効果は繊
維状マグネシウム化合物を配合したものによることが明
らかである。(Evaluation) Clearly from the table! The coating composition of the example containing the 1lIi-form magnesium compound does not cause sagging during drying even when the film thickness is increased, and is far superior to the comparative example. On the other hand, the chipping resistance is 1IIJf is 100μ, 20
Even though it is as thin as 0μ, it shows a value of 9 in the range of 2.5 to 3.5, and has performance equivalent to or higher than that of the comparative example. It is clear that this effect is due to the inclusion of a fibrous magnesium compound.
Claims (4)
、粉質充填剤10〜60重量部と、繊維状充填剤10〜
100重量部と、からなり、金属製品表面に被覆されて
該金属製品をチッピングから保護することを特徴とする
耐チッピング用被覆組成物。(1) 100 parts by weight of water-dispersible acrylic resin in solid content, 10 to 60 parts by weight of powdery filler, and 10 to 60 parts by weight of fibrous filler.
100 parts by weight, and is coated on the surface of a metal product to protect the metal product from chipping.
よび断面の最大径が0.1〜3μmである特許請求の範
囲第1項記載の耐チッピング用被覆組成物。(2) The chipping-resistant coating composition according to claim 1, wherein the single fibers of the fibrous filler have a length of 10 to 200 μm and a maximum cross-sectional diameter of 0.1 to 3 μm.
00である特許請求の範囲第1項記載の耐チッピング用
被覆組成物。(3) The single fiber of the fibrous filler has an aspect ratio of 50 to 2.
00. The chipping-resistant coating composition according to claim 1, which is 00.
脂の固形分100重量部に対し合計で50〜160重量
部配合される特許請求の範囲第1項記載の耐チッピング
用被覆組成物。(4) The chipping-resistant coating composition according to claim 1, wherein the powder filler and the fibrous filler are blended in a total of 50 to 160 parts by weight based on 100 parts by weight of the solid content of the water-dispersible acrylic resin. thing.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP61073440A JPH064784B2 (en) | 1986-03-31 | 1986-03-31 | Coating composition for chipping resistance |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP61073440A JPH064784B2 (en) | 1986-03-31 | 1986-03-31 | Coating composition for chipping resistance |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS62230868A true JPS62230868A (en) | 1987-10-09 |
JPH064784B2 JPH064784B2 (en) | 1994-01-19 |
Family
ID=13518302
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP61073440A Expired - Lifetime JPH064784B2 (en) | 1986-03-31 | 1986-03-31 | Coating composition for chipping resistance |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH064784B2 (en) |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH02219846A (en) * | 1989-02-22 | 1990-09-03 | Honda Motor Co Ltd | Plastisol coating composition for automobile |
GB2241501A (en) * | 1990-03-02 | 1991-09-04 | Cashew Co Ltd | An aqueous coating composition and a metal structure coated thereby |
JPH06207134A (en) * | 1992-11-06 | 1994-07-26 | Nippon Carbide Ind Co Inc | Water-based coating composition |
US5424355A (en) * | 1991-05-17 | 1995-06-13 | Nippon Carbide Kogyo Kabushiki Kaisha | Aqueous coating composition |
JP2003327916A (en) * | 2002-05-16 | 2003-11-19 | Kansai Paint Co Ltd | Water-based coating material composition |
DE4038390B4 (en) * | 1990-12-01 | 2005-03-17 | Henkel Kgaa | Light coloured electrically conductive coatings, seals or bonds - are prepd. from compsn. contg. aq. dispersion of polymer, light coloured conductive metal cpds., and carbon@ fibres |
US7163978B2 (en) | 2002-03-22 | 2007-01-16 | Nippon Carbide Kogyo Kabushiki Kaisha | Waterborne anti-chipping coating composition for automobiles |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5318643A (en) * | 1976-08-04 | 1978-02-21 | Shikoku Kaken Kogyo Kk | Paint for dualllayer patterns |
JPS5538852A (en) * | 1978-09-13 | 1980-03-18 | Dainippon Toryo Co Ltd | Aqueous soundproof paint |
JPS5811566A (en) * | 1981-07-15 | 1983-01-22 | Aisin Chem Co Ltd | Thick intercoating paint for vehicle |
JPS5871968A (en) * | 1981-10-23 | 1983-04-28 | Nippon Paint Co Ltd | Chipping resistant coating material composition |
JPS58117270A (en) * | 1981-12-30 | 1983-07-12 | Nippon Steel Corp | Paint for coating open-air stockpile |
-
1986
- 1986-03-31 JP JP61073440A patent/JPH064784B2/en not_active Expired - Lifetime
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5318643A (en) * | 1976-08-04 | 1978-02-21 | Shikoku Kaken Kogyo Kk | Paint for dualllayer patterns |
JPS5538852A (en) * | 1978-09-13 | 1980-03-18 | Dainippon Toryo Co Ltd | Aqueous soundproof paint |
JPS5811566A (en) * | 1981-07-15 | 1983-01-22 | Aisin Chem Co Ltd | Thick intercoating paint for vehicle |
JPS5871968A (en) * | 1981-10-23 | 1983-04-28 | Nippon Paint Co Ltd | Chipping resistant coating material composition |
JPS58117270A (en) * | 1981-12-30 | 1983-07-12 | Nippon Steel Corp | Paint for coating open-air stockpile |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH02219846A (en) * | 1989-02-22 | 1990-09-03 | Honda Motor Co Ltd | Plastisol coating composition for automobile |
GB2241501A (en) * | 1990-03-02 | 1991-09-04 | Cashew Co Ltd | An aqueous coating composition and a metal structure coated thereby |
DE4038390B4 (en) * | 1990-12-01 | 2005-03-17 | Henkel Kgaa | Light coloured electrically conductive coatings, seals or bonds - are prepd. from compsn. contg. aq. dispersion of polymer, light coloured conductive metal cpds., and carbon@ fibres |
US5424355A (en) * | 1991-05-17 | 1995-06-13 | Nippon Carbide Kogyo Kabushiki Kaisha | Aqueous coating composition |
JPH06207134A (en) * | 1992-11-06 | 1994-07-26 | Nippon Carbide Ind Co Inc | Water-based coating composition |
US7163978B2 (en) | 2002-03-22 | 2007-01-16 | Nippon Carbide Kogyo Kabushiki Kaisha | Waterborne anti-chipping coating composition for automobiles |
JP2003327916A (en) * | 2002-05-16 | 2003-11-19 | Kansai Paint Co Ltd | Water-based coating material composition |
Also Published As
Publication number | Publication date |
---|---|
JPH064784B2 (en) | 1994-01-19 |
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