JPS63218281A - Crack painting process - Google Patents
Crack painting processInfo
- Publication number
- JPS63218281A JPS63218281A JP5241487A JP5241487A JPS63218281A JP S63218281 A JPS63218281 A JP S63218281A JP 5241487 A JP5241487 A JP 5241487A JP 5241487 A JP5241487 A JP 5241487A JP S63218281 A JPS63218281 A JP S63218281A
- Authority
- JP
- Japan
- Prior art keywords
- paint
- cracking
- photosetting
- coated
- undercoat
- 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
- 238000007591 painting process Methods 0.000 title 1
- 239000003973 paint Substances 0.000 claims abstract description 71
- 238000005336 cracking Methods 0.000 claims abstract description 32
- 238000000576 coating method Methods 0.000 claims abstract description 25
- 239000011248 coating agent Substances 0.000 claims abstract description 21
- 238000010438 heat treatment Methods 0.000 claims abstract description 9
- 230000001678 irradiating effect Effects 0.000 claims abstract 3
- 238000001035 drying Methods 0.000 claims description 4
- 230000037303 wrinkles Effects 0.000 abstract description 7
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 abstract description 4
- 239000000020 Nitrocellulose Substances 0.000 abstract description 2
- 238000004519 manufacturing process Methods 0.000 abstract description 2
- 229920001220 nitrocellulos Polymers 0.000 abstract description 2
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 abstract description 2
- 239000000178 monomer Substances 0.000 description 13
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 11
- 238000010422 painting Methods 0.000 description 5
- 229920005989 resin Polymers 0.000 description 4
- 239000011347 resin Substances 0.000 description 4
- 239000004925 Acrylic resin Substances 0.000 description 3
- 229920000178 Acrylic resin Polymers 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 238000007796 conventional method Methods 0.000 description 3
- 239000002537 cosmetic Substances 0.000 description 3
- 238000004132 cross linking Methods 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 description 2
- KWOLFJPFCHCOCG-UHFFFAOYSA-N Acetophenone Chemical compound CC(=O)C1=CC=CC=C1 KWOLFJPFCHCOCG-UHFFFAOYSA-N 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 2
- GUUVPOWQJOLRAS-UHFFFAOYSA-N Diphenyl disulfide Chemical compound C=1C=CC=CC=1SSC1=CC=CC=C1 GUUVPOWQJOLRAS-UHFFFAOYSA-N 0.000 description 2
- ISAOCJYIOMOJEB-UHFFFAOYSA-N benzoin Chemical compound C=1C=CC=CC=1C(O)C(=O)C1=CC=CC=C1 ISAOCJYIOMOJEB-UHFFFAOYSA-N 0.000 description 2
- RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 description 2
- 239000012965 benzophenone Substances 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- CJZGTCYPCWQAJB-UHFFFAOYSA-L calcium stearate Chemical class [Ca+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CJZGTCYPCWQAJB-UHFFFAOYSA-L 0.000 description 2
- 125000004386 diacrylate group Chemical group 0.000 description 2
- GVPWHKZIJBODOX-UHFFFAOYSA-N dibenzyl disulfide Chemical compound C=1C=CC=CC=1CSSCC1=CC=CC=C1 GVPWHKZIJBODOX-UHFFFAOYSA-N 0.000 description 2
- 239000003085 diluting agent Substances 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 2
- 229910052753 mercury Inorganic materials 0.000 description 2
- 229920000728 polyester Polymers 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 238000007592 spray painting technique Methods 0.000 description 2
- HJUGFYREWKUQJT-UHFFFAOYSA-N tetrabromomethane Chemical compound BrC(Br)(Br)Br HJUGFYREWKUQJT-UHFFFAOYSA-N 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- -1 α-haloketone Chemical compound 0.000 description 2
- CWGBFIRHYJNILV-UHFFFAOYSA-N (1,4-diphenyl-1,2,4-triazol-4-ium-3-yl)-phenylazanide Chemical compound C=1C=CC=CC=1[N-]C1=NN(C=2C=CC=CC=2)C=[N+]1C1=CC=CC=C1 CWGBFIRHYJNILV-UHFFFAOYSA-N 0.000 description 1
- MSAHTMIQULFMRG-UHFFFAOYSA-N 1,2-diphenyl-2-propan-2-yloxyethanone Chemical compound C=1C=CC=CC=1C(OC(C)C)C(=O)C1=CC=CC=C1 MSAHTMIQULFMRG-UHFFFAOYSA-N 0.000 description 1
- DKEGCUDAFWNSSO-UHFFFAOYSA-N 1,8-dibromooctane Chemical compound BrCCCCCCCCBr DKEGCUDAFWNSSO-UHFFFAOYSA-N 0.000 description 1
- DLKQHBOKULLWDQ-UHFFFAOYSA-N 1-bromonaphthalene Chemical compound C1=CC=C2C(Br)=CC=CC2=C1 DLKQHBOKULLWDQ-UHFFFAOYSA-N 0.000 description 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- GOXQRTZXKQZDDN-UHFFFAOYSA-N 2-Ethylhexyl acrylate Chemical compound CCCCC(CC)COC(=O)C=C GOXQRTZXKQZDDN-UHFFFAOYSA-N 0.000 description 1
- PTJDGKYFJYEAOK-UHFFFAOYSA-N 2-butoxyethyl prop-2-enoate Chemical compound CCCCOCCOC(=O)C=C PTJDGKYFJYEAOK-UHFFFAOYSA-N 0.000 description 1
- FPKCTSIVDAWGFA-UHFFFAOYSA-N 2-chloroanthracene-9,10-dione Chemical compound C1=CC=C2C(=O)C3=CC(Cl)=CC=C3C(=O)C2=C1 FPKCTSIVDAWGFA-UHFFFAOYSA-N 0.000 description 1
- ZCDADJXRUCOCJE-UHFFFAOYSA-N 2-chlorothioxanthen-9-one Chemical compound C1=CC=C2C(=O)C3=CC(Cl)=CC=C3SC2=C1 ZCDADJXRUCOCJE-UHFFFAOYSA-N 0.000 description 1
- KMNCBSZOIQAUFX-UHFFFAOYSA-N 2-ethoxy-1,2-diphenylethanone Chemical compound C=1C=CC=CC=1C(OCC)C(=O)C1=CC=CC=C1 KMNCBSZOIQAUFX-UHFFFAOYSA-N 0.000 description 1
- WROUWQQRXUBECT-UHFFFAOYSA-N 2-ethylacrylic acid Chemical compound CCC(=C)C(O)=O WROUWQQRXUBECT-UHFFFAOYSA-N 0.000 description 1
- BQZJOQXSCSZQPS-UHFFFAOYSA-N 2-methoxy-1,2-diphenylethanone Chemical compound C=1C=CC=CC=1C(OC)C(=O)C1=CC=CC=C1 BQZJOQXSCSZQPS-UHFFFAOYSA-N 0.000 description 1
- FIHBHSQYSYVZQE-UHFFFAOYSA-N 6-prop-2-enoyloxyhexyl prop-2-enoate Chemical compound C=CC(=O)OCCCCCCOC(=O)C=C FIHBHSQYSYVZQE-UHFFFAOYSA-N 0.000 description 1
- 239000004342 Benzoyl peroxide Substances 0.000 description 1
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 1
- QSJXEFYPDANLFS-UHFFFAOYSA-N Diacetyl Chemical group CC(=O)C(C)=O QSJXEFYPDANLFS-UHFFFAOYSA-N 0.000 description 1
- BWGNESOTFCXPMA-UHFFFAOYSA-N Dihydrogen disulfide Chemical compound SS BWGNESOTFCXPMA-UHFFFAOYSA-N 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- 229920000297 Rayon Polymers 0.000 description 1
- 244000028419 Styrax benzoin Species 0.000 description 1
- 235000000126 Styrax benzoin Nutrition 0.000 description 1
- 235000008411 Sumatra benzointree Nutrition 0.000 description 1
- DAKWPKUUDNSNPN-UHFFFAOYSA-N Trimethylolpropane triacrylate Chemical compound C=CC(=O)OCC(CC)(COC(=O)C=C)COC(=O)C=C DAKWPKUUDNSNPN-UHFFFAOYSA-N 0.000 description 1
- HVVWZTWDBSEWIH-UHFFFAOYSA-N [2-(hydroxymethyl)-3-prop-2-enoyloxy-2-(prop-2-enoyloxymethyl)propyl] prop-2-enoate Chemical compound C=CC(=O)OCC(CO)(COC(=O)C=C)COC(=O)C=C HVVWZTWDBSEWIH-UHFFFAOYSA-N 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 229920000122 acrylonitrile butadiene styrene Polymers 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 229920000180 alkyd Polymers 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229960002130 benzoin Drugs 0.000 description 1
- 235000019400 benzoyl peroxide Nutrition 0.000 description 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
- 239000004566 building material Substances 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 235000013539 calcium stearate Nutrition 0.000 description 1
- 239000008116 calcium stearate Substances 0.000 description 1
- 150000001728 carbonyl compounds Chemical class 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 239000003431 cross linking reagent Substances 0.000 description 1
- KBLWLMPSVYBVDK-UHFFFAOYSA-N cyclohexyl prop-2-enoate Chemical compound C=CC(=O)OC1CCCCC1 KBLWLMPSVYBVDK-UHFFFAOYSA-N 0.000 description 1
- UQLDLKMNUJERMK-UHFFFAOYSA-L di(octadecanoyloxy)lead Chemical compound [Pb+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O UQLDLKMNUJERMK-UHFFFAOYSA-L 0.000 description 1
- BXCOOPLIKAAONJ-UHFFFAOYSA-N di(propan-2-yl)diazene Chemical compound CC(C)N=NC(C)C BXCOOPLIKAAONJ-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 230000003203 everyday effect Effects 0.000 description 1
- 235000019382 gum benzoic Nutrition 0.000 description 1
- 150000004820 halides Chemical class 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
- 238000009434 installation Methods 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- YDKNBNOOCSNPNS-UHFFFAOYSA-N methyl 1,3-benzoxazole-2-carboxylate Chemical compound C1=CC=C2OC(C(=O)OC)=NC2=C1 YDKNBNOOCSNPNS-UHFFFAOYSA-N 0.000 description 1
- 150000001451 organic peroxides Chemical class 0.000 description 1
- 239000003504 photosensitizing agent Substances 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 150000003464 sulfur compounds Chemical class 0.000 description 1
- YRHRIQCWCFGUEQ-UHFFFAOYSA-N thioxanthen-9-one Chemical compound C1=CC=C2C(=O)C3=CC=CC=C3SC2=C1 YRHRIQCWCFGUEQ-UHFFFAOYSA-N 0.000 description 1
- KUAZQDVKQLNFPE-UHFFFAOYSA-N thiram Chemical compound CN(C)C(=S)SSC(=S)N(C)C KUAZQDVKQLNFPE-UHFFFAOYSA-N 0.000 description 1
- 229960002447 thiram Drugs 0.000 description 1
- 239000006097 ultraviolet radiation absorber Substances 0.000 description 1
- 229920006337 unsaturated polyester resin Polymers 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
- 239000002023 wood Substances 0.000 description 1
- XOOUIPVCVHRTMJ-UHFFFAOYSA-L zinc stearate Chemical compound [Zn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O XOOUIPVCVHRTMJ-UHFFFAOYSA-L 0.000 description 1
Abstract
Description
【発明の詳細な説明】
〔従来技術〕
従来、建材等に用いられているクラッキング塗装は、素
材11に熱乾燥型の下塗り塗料を塗装し、この塗膜12
を硬化させた後、クラッキング塗料を塗装し、加熱する
ことによりクラッキング塗料よりなる塗膜13にクラッ
クを形成していた。しかしながら、この方法では、硬化
した下塗り塗膜の上に、これに親和性をもつクラッキン
グ塗料を塗り、塗膜を形成し、この塗膜に無理にクラッ
クを形成させているため、下塗塗膜に比較的軟かい膜で
あることが要求され、その結果クラックの溝14内に多
くのシワ15が残ってしまい、近くでみると外観が余り
よいとは言えず、このような塗装では、たとえば化粧品
容器等の身近かな物品にほどこすことはできなかった。[Detailed Description of the Invention] [Prior Art] Cracking coating, which has been conventionally used for building materials, etc., involves coating a material 11 with a heat-drying undercoating paint, and applying this coating film 12.
After curing, a cracking paint was applied and heated to form cracks in the coating film 13 made of the cracking paint. However, in this method, a cracking paint that has an affinity for the cured undercoat film is applied to form a paint film, and cracks are forcibly formed in this paint film. A relatively soft film is required, and as a result, many wrinkles 15 remain within the crack grooves 14, and when viewed up close, the appearance is not very good. It was not possible to apply it to everyday items such as containers.
又、クラック形成の結果、溝14の部分に下塗り塗料の
塗膜12が表面に現られれるが、従来の下塗り塗料は前
述のように塗膜がやわらかいため、比較的簡単にキズが
つくので、通常、クラック形成後厚くクリア塗装を施し
、耐擦傷性と外観の向上をはかっていた。Furthermore, as a result of the crack formation, a coating film 12 of the undercoat appears on the surface of the groove 14, but as mentioned above, conventional undercoat paints have a soft coating and are relatively easily scratched. Usually, a thick clear coat is applied after crack formation to improve scratch resistance and appearance.
本発明は前述のような従来技術の欠点を解消し、第1図
に示すようにシワの全く無い極めて意匠性の高い塗装表
面を形成することを目的とするものである。The object of the present invention is to eliminate the drawbacks of the prior art as described above, and to form a painted surface that is completely free of wrinkles and has an extremely high design quality, as shown in FIG.
本発明は、クラッキング塗料の下塗り塗料として、熱反
応を殆ど起こさない光硬化型塗料たとえばメチルメタク
リレートを主成分とする紫外線硬化型塗料を被塗物1に
塗装して塗膜2を形成し、これが未硬化状態のうちに、
下塗り塗料とは対照的に熱速乾型であり、かつ塗膜収縮
率が非常に大きく加熱によりその塗膜自体がクラックを
おこす性質を偉えたクラッキング塗料を塗装し、たとえ
ば、約40〜60℃に約5〜10分加熱してクラッキン
グ塗料よりなる塗膜3にクラック4を形成させることに
より、あたかも水の上で膜にヒビ割れが生じるかのごと
く極めて意匠性の高いヒビ割れ模様を形成し、必要に応
じてさらにこの上に光硬化型塗料を塗装した後。In the present invention, as an undercoat for a cracking paint, a photo-curable paint that causes almost no thermal reaction, such as an ultraviolet-curable paint containing methyl methacrylate as a main component, is applied to an object to be coated 1 to form a coating film 2. While uncured,
In contrast to undercoat paints, we apply cracking paints that dry quickly under heat and have a very high shrinkage rate, causing the paint film itself to crack when heated. By heating for about 5 to 10 minutes to form cracks 4 in the coating film 3 made of cracking paint, a highly decorative crack pattern is formed, as if the film were cracked on water. , and then apply further light-curing paint on top of this if necessary.
最後に光エネルギーを照射して光硬化型塗膜を硬化させ
る。Finally, the photocurable coating film is cured by irradiation with light energy.
なお、二工程になるが光エネルギーの照射はクラッキン
グ塗膜形成後に行い、あらためて、光硬化型塗料を上掛
けし、もう一度光エネルギーを照射して上掛は塗料の硬
化を行ってもさしつかえない。Although it is a two-step process, the irradiation with light energy is performed after the cracking coating film is formed, and then the photocurable paint is applied again, and the overlay is irradiated with light energy to harden the paint.
一般に下塗り塗膜の厚みは約5〜40μとくに10〜2
0μが好ましく、クラッキング塗膜の厚みは約5〜30
μで、薄いと細かいヒビ割れが、厚いと大きなヒビ割れ
ができる。Generally, the thickness of the undercoat film is about 5 to 40μ, especially 10 to 2
0 μ is preferable, and the thickness of the cracking coating is about 5 to 30 μm.
When μ is thin, fine cracks occur, and when it is thick, large cracks occur.
本発明の下塗り塗料は、熱による硬化が実質的におこら
ず、いくら加熱しても塗膜はかなり自由に動きうる状態
を保つことができる光硬化型塗料であって、光エネルギ
ーとして紫外線や電子線等が用いられる。The undercoat paint of the present invention is a light-curable paint that does not substantially cure due to heat and can maintain a state in which the paint film can move freely no matter how much it is heated. Lines etc. are used.
本発明の下塗り塗料の主要構成成分は通常、オリゴマー
、モノマーおよび増感剤よりなり、そのオリゴマーとモ
ノマーの好適な組合せ例を示すと、アクリル樹脂系オリ
ゴマーとアクリル系モノマー、アクリル化部とアクリル
系モノマー、アクリル化アルキッド樹脂とアクリル系モ
ノマー、ポリエステルアクリレートとアクリル系モノマ
ー、ポリエーテルアクリレートとアクリル系モノマー、
アクリル化エポキシ樹脂とアクリル系モノマー、アクリ
ル化ポリウレタンとアクリル系モノマー、アクリル化ス
ピラン樹脂とアクリル系モノマーなどがあり、アクリル
系モノマーとしては、アクリル酸、メタクリル酸。The main components of the undercoating paint of the present invention usually consist of oligomers, monomers, and sensitizers. Preferred combinations of oligomers and monomers include acrylic resin oligomers and acrylic monomers, acrylic resin oligomers and acrylic monomers, and acrylic resin oligomers and acrylic monomers. Monomer, acrylated alkyd resin and acrylic monomer, polyester acrylate and acrylic monomer, polyether acrylate and acrylic monomer,
There are acrylated epoxy resins and acrylic monomers, acrylated polyurethane and acrylic monomers, acrylated spirane resins and acrylic monomers, and acrylic monomers include acrylic acid and methacrylic acid.
エタクリル酸又はこれらのエステルが代表的なものであ
る。又、増感剤としては従来公知の光増感剤のうちから
後工程の加熱条件や、使用する光エネルギーの性質等に
対応して好適なものを単独に、又は組合せて選定するこ
とができるが、代表的なものを例示すればカルボニル化
合物たとえばベンゾイン、ベンゾインメチルエーテル、
ベンゾインエチルエーテル、ベンゾインイソプロピルエ
ーテル、ベンゾインイソブチルエーテル、アセトフェノ
ン、2,2−ジェトキシアセトフェノン、ベンゾフェノ
ン、Pyp′−ビスメチルアミノフェノン、チオキサン
トン、2−クロロチオキサントン、ジアセチル、ベンジ
ル、α−ハロケトン、2−クロロアントラキノン等;有
機過酸化物たとえば過酸化ベンゾイル、過酸化ジーt−
ブチル等;アゾ化合物たとえばアゾビスイソブチロニト
リル、2,2′−アゾビスプロパン、m、m’−アゾキ
シスチレン等;ハロゲン化物たとえば四臭化炭素、α−
ブロモナフタリン、1−グロロメチルナフタリン等;硫
黄化合物、ジフェニルジスルフィド、ジベンジルジスル
フィド、ジベンゾチアゾイルジスルフィド、テトラメチ
ルチウラムジスルフィド等がある。Ethacrylic acid or esters thereof are typical. Further, as the sensitizer, suitable ones can be selected singly or in combination from conventionally known photosensitizers depending on the heating conditions of the post-process, the nature of the light energy used, etc. However, typical examples include carbonyl compounds such as benzoin, benzoin methyl ether,
Benzoin ethyl ether, benzoin isopropyl ether, benzoin isobutyl ether, acetophenone, 2,2-jethoxyacetophenone, benzophenone, Pyp'-bismethylaminophenone, thioxanthone, 2-chlorothioxanthone, diacetyl, benzyl, α-haloketone, 2-chloro anthraquinone, etc.; organic peroxides such as benzoyl peroxide, di-t-peroxide;
Butyl, etc.; Azo compounds such as azobisisobutyronitrile, 2,2'-azobispropane, m,m'-azoxystyrene, etc.; Halides such as carbon tetrabromide, α-
Bromonaphthalene, 1-gloromethylnaphthalene, etc.; sulfur compounds, diphenyl disulfide, dibenzyl disulfide, dibenzothiazoyl disulfide, tetramethylthiuram disulfide, etc.
又、これらの光硬化型塗料において従来から使用されて
いるオリゴマーないし樹脂の希釈剤兼架橋剤としての反
応性希釈剤も使用することができる。その代表的なもの
を例示すると、2−エチルへキシルアクリレート、シク
ロヘキシルアクリレート、ブトキシエチルアクリレート
。In addition, reactive diluents that are conventionally used in these photocurable coatings as diluents and crosslinking agents for oligomers or resins can also be used. Representative examples thereof include 2-ethylhexyl acrylate, cyclohexyl acrylate, and butoxyethyl acrylate.
ネオペンチルグリコールジアクリレート、1,6−ヘキ
サンジオールジアクリレート、ポリエチレングリコール
ジアクリレート、トリメチロールプロパントリアクリレ
ート、ペンタエリトリットトリアクリレート、シアツー
ル2,2−ジアクリレート、ポリエステルジアクリレー
ト、不飽和ポリエステル樹脂、ビニルエステル樹脂など
がある。Neopentyl glycol diacrylate, 1,6-hexanediol diacrylate, polyethylene glycol diacrylate, trimethylolpropane triacrylate, pentaerythritol triacrylate, sheatool 2,2-diacrylate, polyester diacrylate, unsaturated polyester resin, vinyl There are ester resins, etc.
なお、本発明における光硬化型塗料には従来から必要に
応じて添加されている各種添加剤、たとえば安定剤、紫
外線吸収剤、溶剤、レベリング剤等が使用できるのは当
然である。It goes without saying that the photocurable coating material of the present invention may contain various conventional additives, such as stabilizers, ultraviolet absorbers, solvents, leveling agents, etc., as needed.
本発明のクラッキング塗料は、前述の光硬化型下塗り塗
料を塗装し、まだウェットの状態にある間に塗装ができ
る性質のものであって、かつ、比較的低温加熱によりす
みやかに塗膜が収縮硬化してクラックを形成する性質を
もつ塗料である。The cracking paint of the present invention has the property that it can be coated with the above-mentioned photocurable undercoat paint while it is still wet, and that the paint film shrinks and hardens quickly by heating at a relatively low temperature. This is a paint that has the property of forming cracks.
代表的なものとしては、樹脂分としてニトロセルロース
を主成分に、クラック形成功剤として、ステアリン酸塩
等を含有する塗料が挙げられる。ステアリン酸塩の具体
例としては、ステアリン酸カルシウム、ステアリン酸鉛
、ステアリン酸亜鉛等がある。A typical example is a paint containing nitrocellulose as the main component as a resin component and stearate as a crack forming agent. Specific examples of stearates include calcium stearate, lead stearate, zinc stearate, and the like.
本発明の被塗物は全く任意であり、何等限定されるもの
ではなく、たとえばプラスチックス、金属、セラミック
ス、木材等をあげることができるが、とくに本発明のク
ラッキング塗装は仕上りが極めてきれいであるため、化
粧品用具、化粧品容器等が好適な被塗物となる。The object to be coated according to the present invention is completely arbitrary and is not limited in any way, and examples include plastics, metals, ceramics, wood, etc., but in particular, the cracking coating according to the present invention has an extremely beautiful finish. Therefore, cosmetic tools, cosmetic containers, etc. are suitable objects to be coated.
本発明の塗装ラインの一例を第4図に示す。 An example of the painting line of the present invention is shown in FIG.
製品取付は装置21において、7〜10m/分で移動す
るコンベアベルトに被塗物を取りつけ。The product is attached in the device 21 by attaching the object to be coated on a conveyor belt that moves at a speed of 7 to 10 m/min.
塗装ブース22におくる。塗装ブースの前段部分23に
おいて、光硬化型塗料によるスプレー塗装を、後段部分
24においてクラッキング塗料によるスプレー塗装を行
い、ひきつづいて、セツティングゾーン25に移動し、
ここに設けられた遠赤外線ランプにより約40〜60℃
にて5〜10分間加熱する。ここでクラック模様が形成
される。Deliver to painting booth 22. In the front part 23 of the painting booth, spray painting is performed with a light-curing paint, and in the rear part 24, spray painting is performed with a cracking paint, and then the booth is moved to the setting zone 25,
Approximately 40 to 60℃ due to the far infrared lamp installed here
Heat for 5 to 10 minutes. A crack pattern is formed here.
つぎに80W/(!lの高圧水銀灯4基を設けた照射ゾ
ーン26を通り、光硬化型塗料の硬化を完了し、冷却ゾ
ーン27で室温に冷却される。Next, it passes through an irradiation zone 26 equipped with four high-pressure mercury lamps of 80 W/(!l) to complete curing of the photocurable paint, and is cooled to room temperature in a cooling zone 27.
本発明は、前述のように下塗り塗料として光硬化型塗料
を選択したことにより、上塗り塗膜のクラッキングに全
く無理を生ずることがないため、あたかも水の上で膜の
ヒビ割れが生ずるように、シワの全くないすばらしい模
様を形成する。しかも下塗り塗料として塗膜が軟かいも
のを必要とせず、たとえばメチルメタクリレートやメチ
ルメタクリレートを主成分とするような塗料を使用でき
るため、その硬化膜は非常に硬い、そのため、クラック
形成により下塗り塗膜が表面にでてきても、この塗膜は
丈夫であるから、従来のように、さらに上かけ塗装を行
うことを必須要件としない利点がある。In the present invention, by selecting a photocurable paint as the undercoat as described above, there is no problem in cracking the topcoat at all, so the cracking of the topcoat is as if the film were to crack on water. Forms a wonderful pattern with no wrinkles. Furthermore, there is no need for a soft undercoat paint, and for example, methyl methacrylate or paints containing methyl methacrylate as a main component can be used, so the cured film is very hard, and cracks can form on the undercoat. Since this coating film is durable even if it comes to the surface, there is an advantage that it is not necessary to perform an additional top coat as in the past.
このように下塗り塗料として硬い塗膜を形成する光硬化
型塗料を使用しているので、全体の仕上りとしても塗膜
の強度が高まり、かつ、生産効率も向上した。Since a photocurable paint that forms a hard film is used as the undercoat, the overall strength of the film is increased, and production efficiency is also improved.
実施例
ABS樹脂にアルミニウムを真空蒸着した化粧用具(コ
ンパクト)に、三菱レイヨン(株)製部品名ダイヤビー
ムとして知られる紫外線架橋硬化型塗料(この塗料はメ
チルメタクリレートを主成分とする樹脂分に、ベンゾフ
ェノン、紫外線吸収剤、シンナー、レベリング剤等より
構成されている)をスプレー塗装し、ウェットの状態の
まま直ちにクラッキング塗装をスプレー塗装した。Example A cosmetic tool (compact) made of ABS resin vacuum-deposited with aluminum was coated with an ultraviolet cross-linking curable paint known as Diabeam manufactured by Mitsubishi Rayon Co., Ltd. (composed of benzophenone, ultraviolet absorber, thinner, leveling agent, etc.) was spray-painted, and cracking paint was immediately applied while still wet.
クラッキング塗料は、武蔵塗料(株)製部品名ニトロン
で知られるクラッキング塗料で、この塗料100部に対
し、80〜100部のシンナーでうすめ粘度14〜20
秒(IHS、NK−2/20℃)に調整したものを使用
した。The cracking paint is manufactured by Musashi Paint Co., Ltd. and is known by the part name Nitron. For 100 parts of this paint, add 80 to 100 parts of thinner to dilute it to a viscosity of 14 to 20.
(IHS, NK-2/20°C) was used.
クラッキング塗料をスプレー塗装した後、約60℃で約
5分間加熱し、紫外線架橋硬化型塗料中の溶剤の蒸発と
クラックの形成を行ない、最終に、高圧水銀灯ランプに
より照射して、紫外線架橋硬化型塗料を完全硬化させた
。これにより、シワのないヒビ割れ模様をもつきれいな
コンパクトが得られた。After spraying the cracking paint, it is heated at about 60°C for about 5 minutes to evaporate the solvent in the UV cross-linking curable paint and forming cracks, and finally, it is irradiated with a high-pressure mercury lamp to form the UV cross-linking curable paint. The paint was completely cured. This resulted in a clean compact with no wrinkles and a cracked pattern.
第1図は本発明の塗装品断面図、第2図、第3図は従来
方法による塗装品断面図。
1・・・被塗物
2・・・下塗りの光硬化型塗料の塗膜
3・・・上塗りのクラッキング塗料の塗膜4・・・クラ
ックの溝 11・・・従来法の被塗物12・・・従
来法の下塗り塗料塗膜
13・・・上塗りのクラッキング塗料の塗膜14・・・
クラックの溝
15・・・クラックの溝部分に生じたシワ16・・・ク
リヤオーバーコート層
21・・・製品取り付は装置 22・・・塗装ブース2
3・・・下塗り塗料のスプレー塗装部位24・・・上塗
り塗料のスプレー塗装部位25・・・セツティングゾー
ンFIG. 1 is a cross-sectional view of a coated product according to the present invention, and FIGS. 2 and 3 are cross-sectional views of a coated product according to a conventional method. 1... Object to be coated 2... Coating film of light curing paint as undercoat 3... Coating film of cracking paint as top coat 4... Crack groove 11... Object to be coated using conventional method 12. ... Conventional method undercoat paint film 13 ... Top coat cracking paint film 14 ...
Crack groove 15...Wrinkles formed in the crack groove 16...Clear overcoat layer 21...Product installation equipment 22...Painting booth 2
3...Setting area sprayed with undercoat 24...Setting area sprayed with topcoat 25...Setting zone
Claims (1)
下塗り塗装し、これが未硬化の段階において、熱速乾型
クラッキング塗料を塗装し、これを加熱して前記クラッ
キング塗料による塗膜にクラックを形成させた後、光エ
ネルギーを照射して光硬化型塗料の塗膜を硬化させるこ
とを特徴とするクラッキング塗装方法。 2、被塗物に、加熱によって硬化しない光硬化型塗料を
下塗り塗装し、これが未硬化の段階において、熱速乾型
クラッキング塗料を塗装し、これを加熱して前記クラッ
キング塗料による塗膜にクラックを形成させ、ついでこ
の上にさらに光硬化型塗料を塗装した後、光エネルギー
を照射して光硬化型塗料の塗膜を硬化させることを特徴
とするクラッキング塗装方法。 3、被塗物に、加熱によって硬化しない光硬化型塗料を
下塗り塗装し、これが未硬化の段階において、熱速乾型
クラッキング塗料を塗装し、これを加熱して前記クラッ
キング塗料による塗膜にクラックを形成させ、これに光
エネルギーを照射して下塗り塗膜を硬化させ、ついでこ
の上にさらに光硬化型塗料を塗装し、これに光エネルギ
ーを照射して光硬化型塗料の塗膜を硬化させることを特
徴とするクラッキング塗装方法。[Scope of Claims] 1. The object to be coated is coated with an undercoat of a light-curable paint that does not harden by heating, and while this is still uncured, a heat-fast-drying cracking paint is applied, and this is heated to cause the cracking. A cracking coating method characterized by forming cracks in a paint film and then irradiating light energy to harden the photocurable paint film. 2. Apply an undercoat to the object to be coated with a light-curable paint that does not harden by heating, and when this is still uncured, apply a heat-fast-drying cracking paint, and heat it to cause cracks in the cracking paint film. 1. A cracking coating method characterized by forming a photocurable paint, then coating a photocurable paint thereon, and then irradiating light energy to harden the photocurable paint film. 3. Apply an undercoat to the object to be coated with a light-curing paint that does not harden by heating, and when this is still uncured, apply a heat-fast-drying cracking paint, and heat it to cause cracks in the cracking paint film. This is then irradiated with light energy to cure the undercoat film, then a photo-curable paint is further applied on top of this, and light energy is irradiated onto this to cure the photo-curable paint film. A cracking coating method characterized by:
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP5241487A JPS63218281A (en) | 1987-03-06 | 1987-03-06 | Crack painting process |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP5241487A JPS63218281A (en) | 1987-03-06 | 1987-03-06 | Crack painting process |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS63218281A true JPS63218281A (en) | 1988-09-12 |
JPH0433504B2 JPH0433504B2 (en) | 1992-06-03 |
Family
ID=12914130
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP5241487A Granted JPS63218281A (en) | 1987-03-06 | 1987-03-06 | Crack painting process |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS63218281A (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH02198671A (en) * | 1989-01-27 | 1990-08-07 | Toagosei Chem Ind Co Ltd | Production of ornaments having luster |
KR100414676B1 (en) * | 2000-12-29 | 2004-01-07 | 김원대 | Method for preparing artificial marble having crack pattern |
KR100695273B1 (en) * | 2005-06-13 | 2007-03-19 | 송요석 | The cracking water paint, and the mixing method of the same |
JP2011088408A (en) * | 2009-10-26 | 2011-05-06 | Nec Corp | Decoration member and method for manufacturing the same |
-
1987
- 1987-03-06 JP JP5241487A patent/JPS63218281A/en active Granted
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH02198671A (en) * | 1989-01-27 | 1990-08-07 | Toagosei Chem Ind Co Ltd | Production of ornaments having luster |
KR100414676B1 (en) * | 2000-12-29 | 2004-01-07 | 김원대 | Method for preparing artificial marble having crack pattern |
KR100695273B1 (en) * | 2005-06-13 | 2007-03-19 | 송요석 | The cracking water paint, and the mixing method of the same |
JP2011088408A (en) * | 2009-10-26 | 2011-05-06 | Nec Corp | Decoration member and method for manufacturing the same |
Also Published As
Publication number | Publication date |
---|---|
JPH0433504B2 (en) | 1992-06-03 |
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