JP3459722B2 - Release film - Google Patents
Release filmInfo
- Publication number
- JP3459722B2 JP3459722B2 JP07445296A JP7445296A JP3459722B2 JP 3459722 B2 JP3459722 B2 JP 3459722B2 JP 07445296 A JP07445296 A JP 07445296A JP 7445296 A JP7445296 A JP 7445296A JP 3459722 B2 JP3459722 B2 JP 3459722B2
- Authority
- JP
- Japan
- Prior art keywords
- resin
- weight
- parts
- film
- coating
- 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.)
- Expired - Fee Related
Links
- 229920005989 resin Polymers 0.000 claims description 38
- 239000011347 resin Substances 0.000 claims description 38
- 229920000180 alkyd Polymers 0.000 claims description 34
- 229920000877 Melamine resin Polymers 0.000 claims description 23
- 239000004640 Melamine resin Substances 0.000 claims description 22
- 239000004925 Acrylic resin Substances 0.000 claims description 21
- 229920000178 Acrylic resin Polymers 0.000 claims description 21
- 229920002050 silicone resin Polymers 0.000 claims description 19
- 238000002156 mixing Methods 0.000 claims description 11
- 239000002985 plastic film Substances 0.000 claims description 10
- 229920006255 plastic film Polymers 0.000 claims description 10
- 239000011342 resin composition Substances 0.000 claims description 10
- 125000000217 alkyl group Chemical group 0.000 claims description 2
- 102000006835 Lamins Human genes 0.000 claims 1
- 108010047294 Lamins Proteins 0.000 claims 1
- 210000005053 lamin Anatomy 0.000 claims 1
- 238000000576 coating method Methods 0.000 description 44
- 239000011248 coating agent Substances 0.000 description 35
- 239000010410 layer Substances 0.000 description 27
- 239000000243 solution Substances 0.000 description 19
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 18
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 18
- 239000000919 ceramic Substances 0.000 description 16
- -1 polyethylene Polymers 0.000 description 16
- 239000007788 liquid Substances 0.000 description 13
- 238000010438 heat treatment Methods 0.000 description 12
- 239000000853 adhesive Substances 0.000 description 10
- 230000001070 adhesive effect Effects 0.000 description 10
- 239000002002 slurry Substances 0.000 description 10
- 239000002904 solvent Substances 0.000 description 10
- 238000000034 method Methods 0.000 description 9
- 229920006267 polyester film Polymers 0.000 description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 9
- 238000006243 chemical reaction Methods 0.000 description 7
- 150000007974 melamines Chemical class 0.000 description 7
- 229920000139 polyethylene terephthalate Polymers 0.000 description 7
- 239000005020 polyethylene terephthalate Substances 0.000 description 7
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 6
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 6
- 239000003377 acid catalyst Substances 0.000 description 6
- 239000012046 mixed solvent Substances 0.000 description 6
- 239000007787 solid Substances 0.000 description 6
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 5
- 239000004820 Pressure-sensitive adhesive Substances 0.000 description 5
- 239000012790 adhesive layer Substances 0.000 description 5
- 239000003973 paint Substances 0.000 description 5
- 229920000728 polyester Polymers 0.000 description 5
- 239000000843 powder Substances 0.000 description 5
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 5
- 229920002125 Sokalan® Polymers 0.000 description 4
- 239000002390 adhesive tape Substances 0.000 description 4
- 239000003960 organic solvent Substances 0.000 description 4
- 239000004584 polyacrylic acid Substances 0.000 description 4
- 229920001296 polysiloxane Polymers 0.000 description 4
- 230000001681 protective effect Effects 0.000 description 4
- 230000001846 repelling effect Effects 0.000 description 4
- 239000007864 aqueous solution Substances 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- 235000004443 Ricinus communis Nutrition 0.000 description 2
- 239000006087 Silane Coupling Agent Substances 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 235000010290 biphenyl Nutrition 0.000 description 2
- 239000004305 biphenyl Substances 0.000 description 2
- 125000006267 biphenyl group Chemical group 0.000 description 2
- 239000004359 castor oil Substances 0.000 description 2
- 235000019438 castor oil Nutrition 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 239000003240 coconut oil Substances 0.000 description 2
- 235000019864 coconut oil Nutrition 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 238000004132 cross linking Methods 0.000 description 2
- 239000004205 dimethyl polysiloxane Substances 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 125000000524 functional group Chemical group 0.000 description 2
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 238000000465 moulding Methods 0.000 description 2
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 2
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 2
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 description 2
- 229910001220 stainless steel Inorganic materials 0.000 description 2
- 239000010935 stainless steel Substances 0.000 description 2
- 239000004094 surface-active agent Substances 0.000 description 2
- JZLWSRCQCPAUDP-UHFFFAOYSA-N 1,3,5-triazine-2,4,6-triamine;urea Chemical class NC(N)=O.NC1=NC(N)=NC(N)=N1 JZLWSRCQCPAUDP-UHFFFAOYSA-N 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- 244000068988 Glycine max Species 0.000 description 1
- 235000010469 Glycine max Nutrition 0.000 description 1
- 240000006240 Linum usitatissimum Species 0.000 description 1
- 235000004431 Linum usitatissimum Nutrition 0.000 description 1
- LGRFSURHDFAFJT-UHFFFAOYSA-N Phthalic anhydride Natural products C1=CC=C2C(=O)OC(=O)C2=C1 LGRFSURHDFAFJT-UHFFFAOYSA-N 0.000 description 1
- 229920002845 Poly(methacrylic acid) Polymers 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 101150000971 SUS3 gene Proteins 0.000 description 1
- 229910004298 SiO 2 Inorganic materials 0.000 description 1
- 229910010413 TiO 2 Inorganic materials 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 238000007259 addition reaction Methods 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 125000003545 alkoxy group Chemical group 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 239000002216 antistatic agent Substances 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 238000007611 bar coating method Methods 0.000 description 1
- JRPBQTZRNDNNOP-UHFFFAOYSA-N barium titanate Chemical compound [Ba+2].[Ba+2].[O-][Ti]([O-])([O-])[O-] JRPBQTZRNDNNOP-UHFFFAOYSA-N 0.000 description 1
- 229910002113 barium titanate Inorganic materials 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- JHIWVOJDXOSYLW-UHFFFAOYSA-N butyl 2,2-difluorocyclopropane-1-carboxylate Chemical compound CCCCOC(=O)C1CC1(F)F JHIWVOJDXOSYLW-UHFFFAOYSA-N 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 238000005266 casting Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 230000002950 deficient Effects 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 150000002009 diols Chemical class 0.000 description 1
- KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical class [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000003912 environmental pollution Methods 0.000 description 1
- 125000003700 epoxy group Chemical group 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
- 239000010419 fine particle Substances 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 235000004426 flaxseed Nutrition 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 239000001023 inorganic pigment Substances 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 1
- 125000005641 methacryl group Chemical group 0.000 description 1
- 238000013508 migration Methods 0.000 description 1
- 230000005012 migration Effects 0.000 description 1
- 239000011259 mixed solution Substances 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 235000019198 oils Nutrition 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 229920001483 poly(ethyl methacrylate) polymer Polymers 0.000 description 1
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
- 229920001515 polyalkylene glycol Polymers 0.000 description 1
- 229920001707 polybutylene terephthalate Polymers 0.000 description 1
- 229920005646 polycarboxylate Polymers 0.000 description 1
- 229920000120 polyethyl acrylate Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 239000004926 polymethyl methacrylate Substances 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 150000007519 polyprotic acids Polymers 0.000 description 1
- 229920005749 polyurethane resin Polymers 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- KVCGISUBCHHTDD-UHFFFAOYSA-M sodium;4-methylbenzenesulfonate Chemical compound [Na+].CC1=CC=C(S([O-])(=O)=O)C=C1 KVCGISUBCHHTDD-UHFFFAOYSA-M 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 125000003396 thiol group Chemical group [H]S* 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
- 238000009736 wetting Methods 0.000 description 1
Landscapes
- Laminated Bodies (AREA)
Description
【0001】[0001]
【発明の属する技術分野】本発明は離型フイルムに関
し、更に詳しくは水系塗料を用いて塗設される粘着剤被
膜の保護フイルムに有用な、或いは水系溶液や水系スラ
リーを用いて成形される樹脂シート、樹脂被膜、セラミ
ックシート等の成形用キャリヤフイルムに有用な、離型
フイルムに関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a release film, and more specifically, a resin useful as a protective film for a pressure-sensitive adhesive coating applied by using an aqueous paint, or a resin formed by using an aqueous solution or an aqueous slurry. The present invention relates to a release film useful as a carrier film for molding sheets, resin coatings, ceramic sheets and the like.
【0002】[0002]
【従来の技術】離型フイルムは、各種粘着剤被膜の保護
フイルムとして広範に使用されている。かかる粘着剤被
膜は、通常ベースフイルムの表面に粘着剤と溶剤とを含
む塗液を塗工した後、加熱して溶媒を除去する方法で塗
設される。そして離型フイルムは、この粘着剤被膜の表
面に積層され保護フイルムとして用いられている。2. Description of the Related Art Release films are widely used as protective films for various adhesive coatings. Such a pressure-sensitive adhesive film is usually applied by a method of applying a coating liquid containing a pressure-sensitive adhesive and a solvent on the surface of the base film and then heating to remove the solvent. The release film is laminated on the surface of the pressure-sensitive adhesive film and used as a protective film.
【0003】また、離型フイルムは、樹脂シート、樹脂
被膜、或はセラミックシート等を成形する際のキャリヤ
フイルムとしても用いられる。例えば、樹脂シートは、
塩化ビニル樹脂等の樹脂溶媒からなる樹脂溶液を離型フ
イルム(キャリヤフイルム)上に塗工(流延)した後、
溶媒を加熱除去することによりマーキングシート用の塩
化ビニルシート等として成形され、キャリヤフイルムか
ら剥離分離されて各種の用途に供される。また樹脂被膜
は、キャリヤフイルムの表面に粘着剤等の樹脂と溶媒か
らなる塗液を塗布した後、加熱して溶媒を除去すること
により被膜成形される。また、セラミックシートは、例
えばセラミック粉体とバインダー剤等とを溶媒に分散さ
せたスラリーをキャリヤフイルム上に塗工した後、溶媒
を加熱除去することによりセラミック生シート(セラミ
ックグリーンシート)として成形される。The release film is also used as a carrier film when molding a resin sheet, a resin film, a ceramic sheet or the like. For example, the resin sheet is
After coating (casting) a resin solution consisting of a resin solvent such as vinyl chloride resin on a release film (carrier film),
The solvent is removed by heating to form a vinyl chloride sheet or the like for a marking sheet, which is peeled off from the carrier film and used for various purposes. The resin film is formed by applying a coating liquid containing a resin such as an adhesive and a solvent on the surface of the carrier film and then heating to remove the solvent. The ceramic sheet is formed as a ceramic green sheet (ceramic green sheet) by, for example, applying a slurry prepared by dispersing ceramic powder and a binder agent in a solvent onto a carrier film and then removing the solvent by heating. It
【0004】上記の溶媒には、従来は有機溶剤が用いら
れていた。しかし最近は有機溶剤に替わって水が用いら
れることが多くなっている。即ち、粘着剤を含む塗液に
はエマルジョン等のような粘着剤の水溶液が用いられ、
スラリーの塗工には水分散スラリーが用いられるように
なった。この理由として、水は有機溶剤のような火災や
環境汚染の危険が無いため、溶液やスラリーの濃度調整
工程、塗工や加熱除去工程等において薬液の取扱いが極
めて容易となることが挙げられる。Organic solvents have hitherto been used as the above-mentioned solvents. However, recently, water is often used instead of the organic solvent. That is, an aqueous solution of an adhesive such as an emulsion is used for the coating liquid containing the adhesive,
A water-dispersed slurry has come to be used for coating the slurry. The reason for this is that water does not pose a risk of fire or environmental pollution like an organic solvent, and therefore it becomes extremely easy to handle the chemical solution in the step of adjusting the concentration of the solution or slurry, the step of coating or the step of removing by heating.
【0005】しかしながら、有機溶剤に比べて水は表面
張力が大きく(水の表面張力γL は73dyne/cm 程
度)、表面エネルギーの小さな離型層(例えばシリコー
ン系離型層の表面張力(γS)は19〜21dyne/cm 程
度)上に粘着剤の水溶液や水分散スラリー等の水性塗液
を塗工した際に、塗液が離型層面に均一に塗れず液滴状
に散在する(いわゆるハジキ)状態となることが大きな
問題となる。この問題を改良するため、塗液(樹脂溶液
やスラリー)を高粘度とする方法や、塗液の表面張力を
低減するために界面活性剤等を配合する方法が考えられ
る。しかしながら、高粘度にする方法では、塗工の際の
レベリングが難しく塗膜厚みが均一になりにくい、また
樹脂シート、樹脂被膜やセラミックシート等の薄層化が
困難という欠点がある。また、界面活性剤を配合する
と、その種類や量によってはシート後のシート強度が低
下し安定したものが得られないことがある等の問題があ
る。However, the surface tension of water is larger than that of organic solvents (the surface tension γL of water is about 73 dyne / cm), and the release layer having a small surface energy (for example, the surface tension (γS) of the silicone release layer is (19 to 21 dyne / cm) When an aqueous coating solution such as an aqueous solution of an adhesive or a water-dispersed slurry is applied onto the surface of the release layer, the coating solution is not uniformly applied and is dispersed in droplets (so-called cissing). It becomes a big problem to be in a state. In order to improve this problem, a method of increasing the viscosity of the coating liquid (resin solution or slurry) or a method of adding a surfactant or the like to reduce the surface tension of the coating liquid can be considered. However, the method of increasing the viscosity has the drawbacks that leveling during coating is difficult and the thickness of the coating film is not uniform, and that it is difficult to thin the resin sheet, the resin coating, the ceramic sheet, or the like. Further, when a surfactant is blended, there is a problem that the sheet strength after the sheet is reduced and a stable product may not be obtained depending on the type and amount thereof.
【0006】[0006]
【発明が解決しようとする課題】本発明の目的は、かか
る従来技術の欠点を解消し、塗工用に水系の塗液を用い
てもハジキが生じない(濡れ性が良い)離型層表面を有
し、各種粘着剤被膜、樹脂シート、セラミックシート等
に対し適度の力で剥離が可能(離型性が良い)である離
型フイルムを提供することにある。The object of the present invention is to solve the above-mentioned drawbacks of the prior art and to prevent cissing even if an aqueous coating solution is used for coating (good wettability). It is intended to provide a release film having the above-mentioned properties and capable of being peeled off from various pressure-sensitive adhesive films, resin sheets, ceramic sheets and the like with an appropriate force (good releasability).
【0007】[0007]
【課題を解決するための手段】本発明の目的は、本発明
によれば、プラスチックフィルムの少なくとも片面に、
アルキッド樹脂、アクリル樹脂及びメラミン樹脂からな
る有機樹脂(ただし、該有機樹脂において、アルキッド
樹脂及びアクリル樹脂の合計100重量部に対しメラミ
ン樹脂は10〜200重量部であり、アルキッド樹脂1
00重量部に対しアクリル樹脂は50〜300重量部で
ある)100重量部に対し、シリコーン樹脂1〜30重
量部を配合して得られる樹脂組成物を主成分とする離型
層を設けた離型フイルムにより達成される。以下、本発
明を詳細に説明する。The object of the invention is, according to the invention, on at least one side of a plastic film,
Organic resin consisting of alkyd resin, acrylic resin and melamine resin (however, in the organic resin, alkyd resin
Melamine for 100 parts by weight of resin and acrylic resin in total
Resin is 10 to 200 parts by weight, and alkyd resin 1
Acrylic resin is 50 to 300 parts by weight with respect to 00 parts by weight.
It is achieved by a release film provided with a release layer whose main component is a resin composition obtained by mixing 1 to 30 parts by weight of a silicone resin with respect to 100 parts by weight. Hereinafter, the present invention will be described in detail.
【0008】[プラスチックフイルム]本発明において
フイルム基材として用いるプラスチックフイルムは、特
に制限はないが、好ましい例としてポリエステルフイル
ム、ポリエチレンやポリプロピレン等のポリオレフィン
フイルム、ポリ塩化ビニルフイルム等を挙げることがで
きる。これらのプラスチックフイルムのうち、フイルム
の耐熱寸法安定性に優れるポリエステルフイルムが特に
好ましい。[Plastic Film] The plastic film used as the film substrate in the present invention is not particularly limited, but preferred examples include polyester film, polyolefin film such as polyethylene and polypropylene, polyvinyl chloride film and the like. Among these plastic films, the polyester film, which is excellent in heat resistance and dimensional stability of the film, is particularly preferable.
【0009】上記のポリエステルフイルムとしては、透
明性が要求される用途には透明性の良好なポリエステル
フイルムを用いることが好ましく、二軸延伸ポリエステ
ルフイルムが特に好ましい。また、遮光性が要求される
用途には無機顔料を配合したポリエステルフイルムを用
いることが好ましく、TiO2 、SiO2 等の如き顔料
を配合した二軸延伸ポリエステルフイルムが特に好まし
い。As the above-mentioned polyester film, a polyester film having good transparency is preferably used for applications requiring transparency, and a biaxially stretched polyester film is particularly preferable. For applications requiring light-shielding properties, a polyester film containing an inorganic pigment is preferably used, and a biaxially stretched polyester film containing a pigment such as TiO 2 or SiO 2 is particularly preferable.
【0010】かかるポリエステルフイルムを構成するポ
リエステルは、芳香族二塩基酸成分とジオール成分とか
らなる結晶性の線状飽和ポリエステルであることが好ま
しく、例えばポリエチレンテレフタレート、ポリプロピ
レンテレフタレート、ポリブチレンテレフタレート、ポ
リエチレン―2,6―ナフタレンジカルボキシレート等
を挙げることができる。また、これらの一部が他成分に
置換された共重合体や、ポリアルキレングリコール或は
他の樹脂との混合物であっても良い。The polyester constituting the polyester film is preferably a crystalline linear saturated polyester composed of an aromatic dibasic acid component and a diol component. For example, polyethylene terephthalate, polypropylene terephthalate, polybutylene terephthalate, polyethylene- 2,6-naphthalene dicarboxylate and the like can be mentioned. Further, it may be a copolymer in which a part of these is substituted with another component, or a mixture with a polyalkylene glycol or another resin.
【0011】上記のポリエステルフイルムは二軸延伸フ
イルムが好ましいが、この二軸延伸フイルムは公知の方
法で製造することができる。例えば、上記ポリエステル
を乾燥後溶融し、ダイ(例えばT−ダイ、I−ダイ等)
から冷却ドラム上に押出し、急冷して未延伸フイルムを
得、続いて該未延伸フイルムを縦方向に2〜5倍の範囲
で延伸し、次いで横方向に2〜5倍の範囲で延伸を行な
い、更に160〜260℃で熱固定することで製造する
ことができる。フイルム厚みには特に制限はないが、5
〜200μmが望ましい。The above polyester film is preferably a biaxially stretched film, but this biaxially stretched film can be manufactured by a known method. For example, the polyester is dried and then melted, and then a die (for example, T-die, I-die, etc.)
From the above to a cooling drum and rapidly cooled to obtain an unstretched film, which is then stretched in the longitudinal direction in the range of 2 to 5 times and then in the transverse direction in the range of 2 to 5 times. Further, it can be produced by further heat fixing at 160 to 260 ° C. The film thickness is not particularly limited, but 5
˜200 μm is desirable.
【0012】かかるプラスチックフイルムには、フイル
ムの滑り性、加工性を良好なものとするため、滑剤、例
えば炭酸カルシウム、カオリン、シリカ、酸化チタン等
のような無機微粒子等を含有させることができ、また他
の添加剤、例えば安定剤、紫外線吸収剤、難燃剤、帯電
防止剤等を含有させることもできる。The plastic film may contain a lubricant, for example, inorganic fine particles such as calcium carbonate, kaolin, silica, titanium oxide, etc. in order to improve the slipperiness and processability of the film. Further, other additives such as stabilizers, ultraviolet absorbers, flame retardants, antistatic agents and the like may be contained.
【0013】[離形層]本発明においては、プラスチッ
クフィルムの少なくとも片面に、有機樹脂とシリコーン
樹脂を配合して得られる樹脂組成物を主成分とする離型
層を設ける。[Release Layer] In the present invention, a release layer containing a resin composition obtained by blending an organic resin and a silicone resin as a main component is provided on at least one surface of the plastic film.
【0014】この有機樹脂とは、アルキッド樹脂、アク
リル樹脂及びメラミン樹脂からなるものであり、その配
合割合はアルキッド樹脂及びアクリル樹脂100重量部
に対しメラミン樹脂10〜200重量部であることが好
ましい。The organic resin is composed of an alkyd resin, an acrylic resin and a melamine resin, and the mixing ratio thereof is preferably 10 to 200 parts by weight with respect to 100 parts by weight of the alkyd resin and the acrylic resin.
【0015】本発明における樹脂組成物のうちアルキッ
ド樹脂およびアクリル樹脂はシリコーン樹脂との配合に
よりその少なくとも1部がシリコーン樹脂との共重合体
を形成し、メラミン樹脂は主としてアルキッド樹脂と架
橋反応して離型層を硬化させるよう作用する。Of the resin composition of the present invention, the alkyd resin and the acrylic resin form a copolymer with at least a part of the silicone resin by blending with the silicone resin, and the melamine resin mainly undergoes a crosslinking reaction with the alkyd resin. It acts to cure the release layer.
【0016】上記のアルキッド樹脂とは、酸成分として
無水フタル酸等の多塩基酸と、グリコール成分としてグ
リセリンやエチレングリコール等の多価アルコールとの
縮合物を骨格とし、これを乾性油等の脂肪酸で変性した
樹脂である。例えば、ヒマシ油変性アルキッド樹脂や大
豆油変性アルキッド樹脂やアマニ油変性アルキッド樹脂
等が用いられるが、任意の組合わせにより、各種脂肪酸
変性のアルキッド樹脂を用いることができる。本発明に
おける樹脂組成物では、例えばアルキッド樹脂の製造中
又は製造後にシリコーン樹脂を配合し、アルキッド樹脂
にシリコーン樹脂をグラフト共重合させることができ
る。このときのアルキッド樹脂とシリコーン樹脂の配合
割合は、アルキッド樹脂100重量部に対しシリコーン
樹脂が1〜30重量部であることが好ましく、特に5〜
10重量部であることが好ましい。The above-mentioned alkyd resin has a skeleton of a condensate of polybasic acid such as phthalic anhydride as an acid component and polyhydric alcohol such as glycerin or ethylene glycol as a glycol component, which is a fatty acid such as a drying oil. It is a resin modified by. For example, castor oil-modified alkyd resin, soybean oil-modified alkyd resin, linseed oil-modified alkyd resin and the like are used, but various fatty acid-modified alkyd resins can be used in any combination. In the resin composition of the present invention, for example, a silicone resin can be blended during or after the production of the alkyd resin, and the silicone resin can be graft-copolymerized with the alkyd resin. At this time, the blending ratio of the alkyd resin and the silicone resin is preferably 1 to 30 parts by weight of the silicone resin, particularly 5 to 100 parts by weight of the alkyd resin.
It is preferably 10 parts by weight.
【0017】アクリル樹脂は、離型層の靭性を強靱なも
のとするため、また離型層表面の濡れ性を良好なものと
するため配合される。このアクリル樹脂としては、例え
ばポリアクリル酸、ポリメタクリル酸、ポリメタクリル
酸メチル等を用いることができる。アルキッド樹脂とア
クリル樹脂の混合比率は、その混合比率によりさまざま
な物性が得られるため目的に応じて変えることができる
が、アルキッド樹脂100重量部に対しアクリル樹脂を
50〜300重量部の比率で用いることが好ましい。The acrylic resin is blended in order to make the release layer tough, and to improve the wettability of the release layer surface. As the acrylic resin, for example, polyacrylic acid, polymethacrylic acid, polymethylmethacrylate, or the like can be used. The mixing ratio of the alkyd resin and the acrylic resin can be changed according to the purpose because various physical properties can be obtained depending on the mixing ratio, but the acrylic resin is used in a ratio of 50 to 300 parts by weight with respect to 100 parts by weight of the alkyd resin. It is preferable.
【0018】メラミン樹脂としては、例えばメチル化メ
ラミン樹脂、ブチル化メラミン樹脂、メチル化尿素メラ
ミン樹脂等を用いることができる。アルキッド樹脂及び
アクリル樹脂に対するメラミン樹脂の混合比率は、アル
キッド樹脂及びアクリル樹脂100重量部に対しメラミ
ン樹脂を10〜200重量部の比率で用いることが好ま
しい。また、この架橋反応の硬化触媒として、例えばパ
ラトルエンスルホン酸ソーダ等の酸性触媒を使用でき
る。As the melamine resin, for example, methylated melamine resin, butylated melamine resin, methylated urea melamine resin and the like can be used. The mixing ratio of the melamine resin to the alkyd resin and the acrylic resin is preferably 10 to 200 parts by weight of the melamine resin with respect to 100 parts by weight of the alkyd resin and the acrylic resin. An acid catalyst such as sodium p-toluenesulfonate can be used as a curing catalyst for this crosslinking reaction.
【0019】シリコーン樹脂は、基本骨格がポリジメチ
ルシロキサンからなるポリマーであるが、アルキッド樹
脂等との相溶性を向上させるため末端や側鎖にフェニル
基やアルキル基等を有することが好ましい。The silicone resin is a polymer having a basic skeleton made of polydimethylsiloxane, but preferably has a phenyl group, an alkyl group or the like at the terminal or side chain in order to improve the compatibility with the alkyd resin and the like.
【0020】[離型層の塗設方法]本発明においては、
プラスチックフイルムの少なくとも片面に上記の離形層
を設けるが、この離形層は例えば前記離形層を構成する
成分を含む塗液をフイルムに塗布し、加熱乾燥及び硬化
させて塗膜を形成させることにより塗設することができ
る。この塗液の塗工方法としては、公知の任意の塗工法
が適用でき、例えばロールコート法、ブレードコート
法、バーコート法等を挙げることができるが、これらの
方法に限定されるものではない。また、塗工乾燥後の離
型層の厚みは0.02〜50μmであることが好まし
く、特に0.1〜1μmであることが好ましい。[Method for coating release layer] In the present invention,
The release layer is provided on at least one surface of the plastic film. For the release layer, for example, a coating liquid containing the components constituting the release layer is applied to the film, dried by heating and cured to form a coating film. It can be applied by coating. As a coating method of this coating liquid, any known coating method can be applied, and examples thereof include a roll coating method, a blade coating method and a bar coating method, but are not limited to these methods. . Further, the thickness of the release layer after coating and drying is preferably 0.02 to 50 μm, and particularly preferably 0.1 to 1 μm.
【0021】[接着層]本発明においては、プラスチッ
クフイルムと離形層との密着性を高めるために、プラス
チックフイルムの少なくとも片面に接着層を設け、該接
着層の上に更に離形層を積層することができる。この接
着層には例えばシランカップリング剤を用いることがで
きる。このシランカップリング剤としては、一般式Y−
Si−X3 で示されるものを挙げることができる。ここ
で、Yは、例えばアミノ基、エポキシ基、ビニル基、メ
タクリル基、メルカプト基等で代表される官能基、Xは
アルコキシ基で代表される加水分解性の官能基を示す。
上記の接着層の好ましい厚みは0.01〜5μm程度で
あり、特に0.02〜2μm程度である。[Adhesive Layer] In the present invention, an adhesive layer is provided on at least one side of the plastic film in order to enhance the adhesion between the plastic film and the release layer, and a release layer is further laminated on the adhesive layer. can do. For this adhesive layer, for example, a silane coupling agent can be used. The silane coupling agent is represented by the general formula Y-
Examples thereof include those represented by Si-X3. Here, Y represents a functional group represented by, for example, an amino group, an epoxy group, a vinyl group, a methacryl group, a mercapto group, and X represents a hydrolyzable functional group represented by an alkoxy group.
The preferable thickness of the adhesive layer is about 0.01 to 5 μm, and particularly about 0.02 to 2 μm.
【0022】[0022]
【実施例】以下、実施例をあげて本発明を更に説明す
る。尚、フイルムの各特性値は下記の方法で測定した。EXAMPLES The present invention will be further described below with reference to examples. The characteristic values of the film were measured by the following methods.
【0023】1.水性塗料の濡れ性
下記組成のセラミック粉体分散スラリーを調整する。
(a)セラミック粉体(チタン酸バリウム):100重
量部
(b)水溶性アクリルエマルジョン:9〜13重量部
(c)水溶性ポリウレタン樹脂:1重量部
(d)ポリカルボン酸アンモニウム:1重量部
(e)水:10〜20重量部
(f)アンモニア:1重量部
セラミック粉体分散スラリーの調整はボールミルにて、
へッグマングラインドゲージで7以上の分散状態となる
ようにして行なう。次いで、このセラミック粉体分散ス
ラリーを1milの間隙を有するストレートエッジアプ
リケーターを用い、離形フィルムの離形層面に塗工し、
110℃にて2分間乾燥後、塗工エッジのハジキの程度
を観察し下記の基準にて溶剤系塗料の耐ハジキ性を評価
した。1. Wettability of water-based paint A ceramic powder dispersion slurry having the following composition is prepared. (A) Ceramic powder (barium titanate): 100 parts by weight (b) Water-soluble acrylic emulsion: 9 to 13 parts by weight (c) Water-soluble polyurethane resin: 1 part by weight (d) Ammonium polycarboxylate: 1 part by weight (E) Water: 10 to 20 parts by weight (f) Ammonia: 1 part by weight A ceramic powder dispersion slurry is prepared with a ball mill.
The Hegman grind gauge is used so that the dispersed state is 7 or more. Next, this ceramic powder dispersed slurry is applied to the release layer surface of the release film using a straight edge applicator having a gap of 1 mil,
After drying at 110 ° C. for 2 minutes, the degree of cissing on the coated edge was observed and the cissing resistance of the solvent-based paint was evaluated according to the following criteria.
【0024】 A:ハジキが観察されない ……濡れ性良好 B:ハジキが若干観察される……濡れ性やや良好 C:ハジキが観察される ……濡れ性不良[0024] A: Repelling is not observed ... Good wettability B: Some repelling is observed ... Slightly good wettability C: Repelling is observed ... Poor wettability
【0025】2.セラミックシートの剥離性
上記の項(1.水系塗料の濡れ性)に記載した方法で形
成されたセラミックシートを離形フイルムより剥離した
際の剥離状態を観察し下記の基準にて剥離性を評価し
た。2. Peelability of ceramic sheet The peeling state when the ceramic sheet formed by the method described in the above section (1. Wetting property of water-based paint) is peeled from the release film is observed and the peelability is evaluated according to the following criteria. did.
【0026】
A:容易に剥離できる ……剥離性良好
B:剥離強度が大きく、す速く引張るとシートが破断す
る……剥離性やや良好
C:シートが破断する ……剥離性不良
D:ハジキのためシート化不可 ……極めて不良A: Easy peeling: Good peeling property B: Peeling strength is large and the sheet breaks when pulled quickly. Peeling property is slightly good. C: Sheet breaks .. Poor peeling property D: Repelling. Cannot be made into a sheet because it is ... extremely defective
【0027】3.残留接着率
ポリエステル粘着テープ(ニットー31B)をJIS・
G4305に規定する冷間圧延ステンレス板(SUS3
04)に貼り付けた後の剥離力を測定し、基礎接着力
(f0 )とする。また、前記ポリエステル粘着テープを
フイルムサンプルの離型層塗設面に2kgの圧着ローラ
ーで圧着し、30秒間放置した後粘着テープを剥がす。
そして剥がした粘着テープを上記のステンレス板に貼
り、該貼り合わせ部の剥離力を測定し、残留接着力
(f)とする。得られた基礎接着力(f0)と残留接着
力(f)より下記式を用いて残留接着率を求める。3. Residual adhesion rate polyester adhesive tape (Knit-31B)
Cold rolled stainless steel plate (SUS3 specified in G4305
The peeling force after being adhered to 04) is measured, and is taken as the basic adhesive force (f 0 ). Further, the polyester adhesive tape is pressure-bonded to the release layer coated surface of the film sample with a 2 kg pressure roller, left for 30 seconds, and then the adhesive tape is peeled off.
Then, the peeled adhesive tape is attached to the above-mentioned stainless steel plate, and the peeling force of the bonded portion is measured to obtain the residual adhesive force (f). The residual adhesion ratio is calculated from the obtained basic adhesive force (f 0 ) and residual adhesive force (f) using the following formula.
【0028】[0028]
【数1】残留接着率(%)=(f/f0 )×100
尚、残留接着率の好ましい範囲は85%以上である。残
留接着率が85%未満であると、例えば離型フイルムを
ロール状に巻いて保管する際に、離型層を構成する成分
が隣接するフイルムの表面に転写(いわゆる背面転写)
し、離型層の濡れ性や剥離性等の特性が不良となること
があるため好ましくない。## EQU1 ## Residual adhesion rate (%) = (f / f 0 ) × 100 The preferred range of the residual adhesion rate is 85% or more. When the residual adhesion ratio is less than 85%, for example, when the release film is wound into a roll and stored, the components constituting the release layer are transferred to the surface of the adjacent film (so-called back surface transfer).
However, the wettability and releasability of the release layer may be deteriorated, which is not preferable.
【0029】[実施例1]アルキッド樹脂(ヤシ油変性
アルキッド樹脂)100重量部、アクリル樹脂(ポリア
クリル酸)200重量部、メラミン樹脂(ブチル化メラ
ミン樹脂)50重量部およびシリコーン樹脂(ポリフェ
ニルメチルシロキサン)35重量部(有機樹脂100重
量部に対しシリコーン樹脂10重量部の割合)を混合し
て得られた樹脂組成物をメチルエチルケトン、メチルイ
ソブチルケトン及びトルエンの混合溶剤中に溶解させ、
全体の固形分濃度が3重量%の溶液を作成した。次い
で、硬化反応の促進剤として酸触媒(パラトルエンスル
ホン酸)を上記溶液に添加して塗液を作成した。Example 1 100 parts by weight of alkyd resin (coconut oil modified alkyd resin), 200 parts by weight of acrylic resin (polyacrylic acid), 50 parts by weight of melamine resin (butylated melamine resin) and silicone resin (polyphenylmethyl). Siloxane) 35 parts by weight (ratio of 10 parts by weight of silicone resin to 100 parts by weight of organic resin) is mixed to obtain a resin composition, which is dissolved in a mixed solvent of methyl ethyl ketone, methyl isobutyl ketone and toluene,
A solution having a total solid content concentration of 3% by weight was prepared. Next, an acid catalyst (paratoluenesulfonic acid) was added to the above solution as a curing reaction accelerator to prepare a coating liquid.
【0030】この塗液を厚み50μmの二軸延伸ポリエ
チレンテレフタレートフイルム上に塗布量6g/m2
(wet)で塗布し、加熱温度140℃、時間1分で乾
燥及び硬化させて、離型層の厚さ0.3μmの離型フイ
ルムを作成した。この離型フイルムの特性を表1に示
す。A coating amount of 6 g / m 2 was applied to a biaxially stretched polyethylene terephthalate film having a thickness of 50 μm.
It was applied by (wet) and dried and cured at a heating temperature of 140 ° C. for 1 minute to prepare a release film having a release layer thickness of 0.3 μm. The characteristics of this release film are shown in Table 1.
【0031】[実施例2]アルキッド樹脂(ヒマシ油変
性アルキッド樹脂)100重量部、アクリル樹脂(ポリ
アクリル酸エチル)100重量部、メラミン樹脂(ブチ
ル化メラミン樹脂)100重量部およびシリコーン樹脂
(ヒドロキシル基置換ジフェニルポリシロキサン)75
重量部(有機樹脂100重量部に対しシリコーン樹脂2
5重量部の割合)を混合して得られた樹脂組成物をメチ
ルエチルケトン、メチルイソブチルケトン及びトルエン
の混合溶剤中に溶解させ、全体の固形分濃度が3重量%
の溶液を作成した。次いで、硬化反応の促進剤として酸
触媒(パラトルエンスルホン酸)を上記溶液に添加して
塗液を作成した。Example 2 100 parts by weight of alkyd resin (castor oil modified alkyd resin), 100 parts by weight of acrylic resin (polyethyl acrylate), 100 parts by weight of melamine resin (butylated melamine resin) and silicone resin (hydroxyl group). Substituted diphenyl polysiloxane) 75
Parts by weight (2 parts by weight of silicone resin for 100 parts by weight of organic resin)
The resin composition obtained by mixing 5 parts by weight) is dissolved in a mixed solvent of methyl ethyl ketone, methyl isobutyl ketone and toluene, and the total solid content concentration is 3% by weight.
A solution of was prepared. Next, an acid catalyst (paratoluenesulfonic acid) was added to the above solution as a curing reaction accelerator to prepare a coating liquid.
【0032】この塗液を厚み50μmの二軸延伸ポリエ
チレンテレフタレートフイルム上に塗布量6g/m2
(wet)で塗布し、加熱温度140℃、時間1分で乾
燥及び硬化させて、離型層の厚さ0.3μmの離型フイ
ルムを作成した。この離型フイルムの特性を表1に示
す。A coating amount of 6 g / m 2 was applied to a biaxially stretched polyethylene terephthalate film having a thickness of 50 μm.
It was applied by (wet) and dried and cured at a heating temperature of 140 ° C. for 1 minute to prepare a release film having a release layer thickness of 0.3 μm. The characteristics of this release film are shown in Table 1.
【0033】[実施例3]アルキッド樹脂(ヒマシ油変
性アルキッド樹脂)100重量部、アクリル樹脂(ポリ
アクリル酸100重量部およびポリメタクリル酸エチル
100重量部)200重量部、メラミン樹脂(ブチル化
メラミン樹脂)100重量部およびシリコーン樹脂(ヒ
ドロキシル基置換ジフェニルポリシロキサン)80重量
部(有機樹脂100重量部に対しシリコーン樹脂20重
量部の割合)を混合して得られた樹脂組成物をメチルエ
チルケトン、メチルイソブチルケトン及びトルエンの混
合溶剤中に溶解させ、全体の固形分濃度が3重量%の溶
液を作成した。次いで、硬化反応の促進剤として酸触媒
(パラトルエンスルホン酸)を上記溶液に添加して塗液
を作成した。Example 3 100 parts by weight of alkyd resin (castor oil-modified alkyd resin), 200 parts by weight of acrylic resin (100 parts by weight of polyacrylic acid and 100 parts by weight of polyethyl methacrylate), melamine resin (butylated melamine resin) ) 100 parts by weight and 80 parts by weight of silicone resin (hydroxyl group-substituted diphenylpolysiloxane) (ratio of 20 parts by weight of silicone resin to 100 parts by weight of organic resin) are mixed to obtain methyl ethyl ketone, methyl isobutyl ketone. And was dissolved in a mixed solvent of toluene to prepare a solution having a total solid content concentration of 3% by weight. Next, an acid catalyst (paratoluenesulfonic acid) was added to the above solution as a curing reaction accelerator to prepare a coating liquid.
【0034】この塗液を厚み50μmの二軸延伸ポリエ
チレンテレフタレートフイルム上に塗布量6g/m2
(wet)で塗布し、加熱温度140℃、時間1分で乾
燥及び硬化させて、離型層の厚さ0.3μmの離型フイ
ルムを作成した。この離型フイルムの特性を表1に示
す。A coating amount of 6 g / m 2 was applied to a biaxially stretched polyethylene terephthalate film having a thickness of 50 μm.
It was applied by (wet) and dried and cured at a heating temperature of 140 ° C. for 1 minute to prepare a release film having a release layer thickness of 0.3 μm. The characteristics of this release film are shown in Table 1.
【0035】[比較例1]ポリジメチルシロキサンとジ
メチルハイドロジェンシランの混合溶液に白金触媒を加
えて付加反応させるタイプの硬化型シリコーン(信越化
学工業(株)製・KS847(H))をメチルエチルケ
トン、メチルイソブチルケトン及びトルエンの混合溶剤
中に溶解させ、固形分濃度が2%の溶液を作成した。[Comparative Example 1] A curable silicone (KS847 (H) manufactured by Shin-Etsu Chemical Co., Ltd.) of a type in which a platinum catalyst is added to a mixed solution of polydimethylsiloxane and dimethylhydrogensilane to carry out an addition reaction with methyl ethyl ketone, It was dissolved in a mixed solvent of methyl isobutyl ketone and toluene to prepare a solution having a solid content concentration of 2%.
【0036】この溶液を前記二軸延伸ポリエチレンテレ
フタートフイルム上に塗布量6g/m2 (wet)で塗
布し、加熱温度140℃、時間1分で乾燥及び硬化させ
て、離型層の厚さ0.15μmの離型フイルムを作成し
た。このフイルムの特性を表1に示す。This solution was coated on the biaxially stretched polyethylene terephthalate film at a coating amount of 6 g / m 2 (wet) and dried and cured at a heating temperature of 140 ° C. for 1 minute to give a release layer of 0 thickness. A release film of 0.15 μm was prepared. The characteristics of this film are shown in Table 1.
【0037】[比較例2]アルキッド樹脂(ヤシ油変性
アルキッド樹脂)100重量部およびメラミン樹脂(ブ
チル化メラミン樹脂)40重量部を混合して得られた樹
脂組成物をメチルエチルケトン、メチルイソブチルケト
ン及びトルエンの混合溶剤中に溶解させ、全体の固形分
濃度が3重量%の溶液を作成した。次いで、硬化反応の
促進剤として酸触媒(パラトルエンスルホン酸)を上記
溶液に添加して塗液を作成した。[Comparative Example 2] A resin composition obtained by mixing 100 parts by weight of an alkyd resin (coconut oil modified alkyd resin) and 40 parts by weight of a melamine resin (butylated melamine resin) with methyl ethyl ketone, methyl isobutyl ketone and toluene. Was dissolved in the mixed solvent of to prepare a solution having a total solid content concentration of 3% by weight. Next, an acid catalyst (paratoluenesulfonic acid) was added to the above solution as a curing reaction accelerator to prepare a coating liquid.
【0038】この塗液を厚み50μmの二軸延伸ポリエ
チレンテレフタレートフイルム上に塗布量6g/m2
(wet)で塗布し、加熱温度140℃、時間1分で乾
燥及び硬化させて、離型層の厚さ0.3μmの離型フイ
ルムを作成した。この離型フイルムの特性を表1に示
す。A coating amount of 6 g / m 2 was applied to a biaxially stretched polyethylene terephthalate film having a thickness of 50 μm.
It was applied by (wet) and dried and cured at a heating temperature of 140 ° C. for 1 minute to prepare a release film having a release layer thickness of 0.3 μm. The characteristics of this release film are shown in Table 1.
【0039】[比較例3]アルキッド樹脂(ヒマシ油変
性アルキッド樹脂)100重量部、アクリル樹脂(ポリ
アクリル酸)100重量部、メラミン樹脂(ブチル化メ
ラミン樹脂)100重量部およびシリコーン樹脂(ヒド
ロキシル基置換ジフェニルポリシロキサン)150重量
部(有機樹脂100重量部に対しシリコーン樹脂50重
量部の割合)を混合して得られた樹脂組成物をメチルエ
チルケトン、メチルイソブチルケトン及びトルエンの混
合溶剤中に溶解させ、全体の固形分濃度が3重量%の溶
液を作成した。次いで、硬化反応の促進剤として酸触媒
(パラトルエンスルホン酸)を上記溶液に添加して塗液
を作成した。Comparative Example 3 100 parts by weight of alkyd resin (castor oil modified alkyd resin), 100 parts by weight of acrylic resin (polyacrylic acid), 100 parts by weight of melamine resin (butylated melamine resin) and silicone resin (hydroxyl group substitution) Diphenyl polysiloxane) 150 parts by weight (50 parts by weight of silicone resin to 100 parts by weight of organic resin) are mixed to obtain a resin composition, which is dissolved in a mixed solvent of methyl ethyl ketone, methyl isobutyl ketone and toluene, A solution having a solid content concentration of 3% by weight was prepared. Next, an acid catalyst (paratoluenesulfonic acid) was added to the above solution as a curing reaction accelerator to prepare a coating liquid.
【0040】この塗液を厚み50μmの二軸延伸ポリエ
チレンテレフタレートフイルム上に塗布量6g/m2
(wet)で塗布し、加熱温度140℃、時間1分で乾
燥及び硬化させて、離型層の厚さ0.3μmの離型フイ
ルムを作成した。この離型フイルムの特性を表1に示
す。A coating amount of 6 g / m 2 was applied to a biaxially stretched polyethylene terephthalate film having a thickness of 50 μm.
It was applied by (wet) and dried and cured at a heating temperature of 140 ° C. for 1 minute to prepare a release film having a release layer thickness of 0.3 μm. The characteristics of this release film are shown in Table 1.
【0041】[0041]
【表1】 [Table 1]
【0042】表1より明らかなように、実施例に示した
本発明の離型フイルムは表面の濡れ性、即ち水系塗料に
対する耐ハジキ性、樹脂シートの剥離性、塗膜の非移行
性に優れるものであった。As is clear from Table 1, the release films of the present invention shown in the examples are excellent in surface wettability, that is, cissing resistance to water-based paint, releasability of resin sheet, and non-migration property of coating film. It was a thing.
【0043】[0043]
【発明の効果】本発明の離型フイルムは、離型層にアル
キッド樹脂、アクリル樹脂、メラミン樹脂及びシリコー
ン樹脂からなる樹脂組成物を硬化させた被膜を用いるこ
とで、各種被膜やシート成形用に水系塗液を用いた際に
濡れ性に優れ、また各種樹脂シート、樹脂被膜やセラミ
ックシート等に対する剥離性に優れるため、粘着剤被膜
の保護フイルムや樹脂シート、樹脂被膜、セラミックシ
ート等の成形用キャリヤーフイルムに有用である。EFFECTS OF THE INVENTION The release film of the present invention is used for forming various types of films and sheets by using a film obtained by curing a resin composition composed of an alkyd resin, an acrylic resin, a melamine resin and a silicone resin as a release layer. Excellent in wettability when used with water-based coating liquid, and also excellent in releasability from various resin sheets, resin coatings, ceramic sheets, etc., so for forming protective films for adhesive coatings, resin sheets, resin coatings, ceramic sheets, etc. It is useful as a carrier film.
───────────────────────────────────────────────────── フロントページの続き (56)参考文献 特開 平7−137218(JP,A) 特開 平3−17146(JP,A) 特開 平7−242829(JP,A) 特開 昭51−125102(JP,A) 特開 昭54−119533(JP,A) 特開 平6−23746(JP,A) (58)調査した分野(Int.Cl.7,DB名) B32B 1/00 - 35/00 ─────────────────────────────────────────────────── --Continued from the front page (56) Reference JP-A-7-137218 (JP, A) JP-A-3-17146 (JP, A) JP-A-7-242829 (JP, A) JP-A-51- 125102 (JP, A) JP 54-119533 (JP, A) JP 6-23746 (JP, A) (58) Fields investigated (Int.Cl. 7 , DB name) B32B 1/00-35 / 00
Claims (2)
に、アルキッド樹脂、アクリル樹脂及びメラミン樹脂か
らなる有機樹脂(ただし、該有機樹脂において、アルキ
ッド樹脂及びアクリル樹脂の合計100重量部に対しメ
ラミン樹脂は10〜200重量部であり、アルキッド樹
脂100重量部に対しアクリル樹脂は50〜300重量
部である)100重量部に対し、シリコーン樹脂1〜3
0重量部を配合して得られる樹脂組成物を主成分とする
離型層を設けた離型フイルム。1. An organic resin comprising an alkyd resin, an acrylic resin and a melamine resin on at least one side of a plastic film (provided that the organic resin is an alkyl resin).
For total 100 parts by weight of resin and acrylic resin,
The lamin resin is 10 to 200 parts by weight.
50 to 300 parts by weight of acrylic resin for 100 parts by weight of fat
Parts) 100 parts by weight of silicone resin 1 to 3
A release film provided with a release layer containing a resin composition obtained by blending 0 part by weight as a main component.
樹脂100重量部に対しメラミン樹脂10〜200重量
部からなる請求項1記載の離形フィルム。2. The release film according to claim 1, wherein the organic resin comprises 10 to 200 parts by weight of a melamine resin with respect to 100 parts by weight of an alkyd resin and an acrylic resin.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP07445296A JP3459722B2 (en) | 1996-03-28 | 1996-03-28 | Release film |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP07445296A JP3459722B2 (en) | 1996-03-28 | 1996-03-28 | Release film |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH09262936A JPH09262936A (en) | 1997-10-07 |
JP3459722B2 true JP3459722B2 (en) | 2003-10-27 |
Family
ID=13547655
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP07445296A Expired - Fee Related JP3459722B2 (en) | 1996-03-28 | 1996-03-28 | Release film |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP3459722B2 (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2009083271A (en) * | 2007-09-28 | 2009-04-23 | Tdk Corp | Method for producing laminated film and laminated ceramic electronic component |
KR20170073619A (en) | 2014-10-17 | 2017-06-28 | 신에쓰 가가꾸 고교 가부시끼가이샤 | Heavy release additive for release sheet, organopolysiloxane composition for release sheet, and release sheet |
KR102057297B1 (en) | 2012-12-26 | 2019-12-18 | 도레이첨단소재 주식회사 | Release film for inmold injection molding and manufacturing method thereof |
Families Citing this family (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH11300894A (en) * | 1998-04-16 | 1999-11-02 | Shin Etsu Chem Co Ltd | Release film for process |
JP3337132B2 (en) * | 1998-06-18 | 2002-10-21 | 東洋紡績株式会社 | Polyester film for transfer |
KR20000059814A (en) * | 1999-03-09 | 2000-10-05 | 한형수 | Method for processing release film for aquaeous slurry coatings |
KR100601797B1 (en) * | 2003-12-02 | 2006-07-14 | 도레이새한 주식회사 | Silicone Release Polyester Film |
TWI548318B (en) * | 2007-09-11 | 2016-09-01 | Ajinomoto Kk | Manufacturing method of multilayer printed circuit board |
JP5423975B2 (en) * | 2010-03-29 | 2014-02-19 | Tdk株式会社 | Release film, release film roll, ceramic component sheet, and method for producing ceramic component |
JP5423976B2 (en) * | 2010-03-29 | 2014-02-19 | Tdk株式会社 | Release film manufacturing method, ceramic component sheet manufacturing method, and ceramic component manufacturing method |
WO2016158592A1 (en) | 2015-03-27 | 2016-10-06 | リンテック株式会社 | Releasing film for ceramic green sheet production step |
JPWO2022209547A1 (en) * | 2021-03-30 | 2022-10-06 |
-
1996
- 1996-03-28 JP JP07445296A patent/JP3459722B2/en not_active Expired - Fee Related
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2009083271A (en) * | 2007-09-28 | 2009-04-23 | Tdk Corp | Method for producing laminated film and laminated ceramic electronic component |
KR102057297B1 (en) | 2012-12-26 | 2019-12-18 | 도레이첨단소재 주식회사 | Release film for inmold injection molding and manufacturing method thereof |
KR20170073619A (en) | 2014-10-17 | 2017-06-28 | 신에쓰 가가꾸 고교 가부시끼가이샤 | Heavy release additive for release sheet, organopolysiloxane composition for release sheet, and release sheet |
US10570234B2 (en) | 2014-10-17 | 2020-02-25 | Shin-Etsu Chemical Co., Ltd. | Heavy release additive for release sheet, organopolysiloxane composition for release sheet, and release sheet |
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