JPH0242080B2 - - Google Patents
Info
- Publication number
- JPH0242080B2 JPH0242080B2 JP9606583A JP9606583A JPH0242080B2 JP H0242080 B2 JPH0242080 B2 JP H0242080B2 JP 9606583 A JP9606583 A JP 9606583A JP 9606583 A JP9606583 A JP 9606583A JP H0242080 B2 JPH0242080 B2 JP H0242080B2
- Authority
- JP
- Japan
- Prior art keywords
- transfer material
- molding
- base sheet
- resin
- layer
- 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
Links
- 238000012546 transfer Methods 0.000 claims description 60
- 239000000463 material Substances 0.000 claims description 54
- 238000000465 moulding Methods 0.000 claims description 40
- 229920005989 resin Polymers 0.000 claims description 35
- 239000011347 resin Substances 0.000 claims description 35
- 238000001746 injection moulding Methods 0.000 claims description 21
- 238000010422 painting Methods 0.000 claims description 19
- 239000002985 plastic film Substances 0.000 claims description 11
- 229920006255 plastic film Polymers 0.000 claims description 11
- 230000004927 fusion Effects 0.000 claims description 6
- 238000004519 manufacturing process Methods 0.000 claims description 6
- 238000002347 injection Methods 0.000 claims description 5
- 239000007924 injection Substances 0.000 claims description 5
- 230000002265 prevention Effects 0.000 claims description 5
- 239000010410 layer Substances 0.000 description 43
- 238000000034 method Methods 0.000 description 26
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 21
- 238000013461 design Methods 0.000 description 16
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 15
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 12
- 239000000203 mixture Substances 0.000 description 12
- 239000012790 adhesive layer Substances 0.000 description 11
- 229920000178 Acrylic resin Polymers 0.000 description 8
- 239000004925 Acrylic resin Substances 0.000 description 8
- 229920006267 polyester film Polymers 0.000 description 7
- 239000011241 protective layer Substances 0.000 description 7
- 238000010023 transfer printing Methods 0.000 description 7
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 6
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 6
- -1 and Bengara Chemical compound 0.000 description 6
- 238000007639 printing Methods 0.000 description 6
- 229920001169 thermoplastic Polymers 0.000 description 6
- 229920002803 thermoplastic polyurethane Polymers 0.000 description 6
- 239000004416 thermosoftening plastic Substances 0.000 description 6
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 5
- 230000003141 anti-fusion Effects 0.000 description 5
- 238000000576 coating method Methods 0.000 description 5
- 239000000049 pigment Substances 0.000 description 5
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- 229920006026 co-polymeric resin Polymers 0.000 description 4
- 238000001816 cooling Methods 0.000 description 4
- 238000001035 drying Methods 0.000 description 4
- 229920001971 elastomer Polymers 0.000 description 4
- 239000003822 epoxy resin Substances 0.000 description 4
- 229920003023 plastic Polymers 0.000 description 4
- 239000004033 plastic Substances 0.000 description 4
- 229920000647 polyepoxide Polymers 0.000 description 4
- 239000005060 rubber Substances 0.000 description 4
- 229920005992 thermoplastic resin Polymers 0.000 description 4
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 239000004743 Polypropylene Substances 0.000 description 3
- 229920000122 acrylonitrile butadiene styrene Polymers 0.000 description 3
- 239000012461 cellulose resin Substances 0.000 description 3
- 239000011248 coating agent Substances 0.000 description 3
- 239000003086 colorant Substances 0.000 description 3
- 238000003851 corona treatment Methods 0.000 description 3
- 238000005516 engineering process Methods 0.000 description 3
- 238000007756 gravure coating Methods 0.000 description 3
- 229920006284 nylon film Polymers 0.000 description 3
- 239000003208 petroleum Substances 0.000 description 3
- 239000004014 plasticizer Substances 0.000 description 3
- 229920001155 polypropylene Polymers 0.000 description 3
- 238000011160 research Methods 0.000 description 3
- 230000000630 rising effect Effects 0.000 description 3
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- 229920000877 Melamine resin Polymers 0.000 description 2
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 2
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 2
- 229920001807 Urea-formaldehyde Polymers 0.000 description 2
- 239000012752 auxiliary agent Substances 0.000 description 2
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 2
- 229920006217 cellulose acetate butyrate Polymers 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 238000010017 direct printing Methods 0.000 description 2
- 239000002270 dispersing agent Substances 0.000 description 2
- 239000000975 dye Substances 0.000 description 2
- 238000010894 electron beam technology Methods 0.000 description 2
- 230000001747 exhibiting effect Effects 0.000 description 2
- 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 2
- 239000000025 natural resin Substances 0.000 description 2
- 229920006122 polyamide resin Polymers 0.000 description 2
- 229920001225 polyester resin Polymers 0.000 description 2
- 239000004645 polyester resin Substances 0.000 description 2
- 229920000098 polyolefin Polymers 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 229920006230 thermoplastic polyester resin Polymers 0.000 description 2
- 229920001187 thermosetting polymer Polymers 0.000 description 2
- GZVHEAJQGPRDLQ-UHFFFAOYSA-N 6-phenyl-1,3,5-triazine-2,4-diamine Chemical compound NC1=NC(N)=NC(C=2C=CC=CC=2)=N1 GZVHEAJQGPRDLQ-UHFFFAOYSA-N 0.000 description 1
- 239000004640 Melamine resin Substances 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- NRCMAYZCPIVABH-UHFFFAOYSA-N Quinacridone Chemical compound N1C2=CC=CC=C2C(=O)C2=C1C=C1C(=O)C3=CC=CC=C3NC1=C2 NRCMAYZCPIVABH-UHFFFAOYSA-N 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- 239000003377 acid catalyst Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 229920000180 alkyd Polymers 0.000 description 1
- PYKYMHQGRFAEBM-UHFFFAOYSA-N anthraquinone Natural products CCC(=O)c1c(O)c2C(=O)C3C(C=CC=C3O)C(=O)c2cc1CC(=O)OC PYKYMHQGRFAEBM-UHFFFAOYSA-N 0.000 description 1
- 150000004056 anthraquinones Chemical class 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
- 125000000751 azo group Chemical group [*]N=N[*] 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- QHIWVLPBUQWDMQ-UHFFFAOYSA-N butyl prop-2-enoate;methyl 2-methylprop-2-enoate;prop-2-enoic acid Chemical compound OC(=O)C=C.COC(=O)C(C)=C.CCCCOC(=O)C=C QHIWVLPBUQWDMQ-UHFFFAOYSA-N 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 229910052570 clay Inorganic materials 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 230000008602 contraction Effects 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- PPSZHCXTGRHULJ-UHFFFAOYSA-N dioxazine Chemical compound O1ON=CC=C1 PPSZHCXTGRHULJ-UHFFFAOYSA-N 0.000 description 1
- 208000028659 discharge Diseases 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000011888 foil Substances 0.000 description 1
- 239000011256 inorganic filler Substances 0.000 description 1
- 229910003475 inorganic filler Inorganic materials 0.000 description 1
- 239000001023 inorganic pigment Substances 0.000 description 1
- 239000005001 laminate film Substances 0.000 description 1
- 239000002075 main ingredient Substances 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- IEQIEDJGQAUEQZ-UHFFFAOYSA-N phthalocyanine Chemical compound N1C(N=C2C3=CC=CC=C3C(N=C3C4=CC=CC=C4C(=N4)N3)=N2)=C(C=CC=C2)C2=C1N=C1C2=CC=CC=C2C4=N1 IEQIEDJGQAUEQZ-UHFFFAOYSA-N 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 239000002952 polymeric resin Substances 0.000 description 1
- 229920005672 polyolefin resin Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 238000007650 screen-printing Methods 0.000 description 1
- 238000005728 strengthening Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- AAAQKTZKLRYKHR-UHFFFAOYSA-N triphenylmethane Chemical compound C1=CC=CC=C1C(C=1C=CC=CC=1)C1=CC=CC=C1 AAAQKTZKLRYKHR-UHFFFAOYSA-N 0.000 description 1
- 239000006097 ultraviolet radiation absorber Substances 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 230000037303 wrinkles Effects 0.000 description 1
Landscapes
- Printing Methods (AREA)
- Decoration By Transfer Pictures (AREA)
Description
【発明の詳細な説明】
本発明は成形同時絵付用転写材に関するもので
あり、更に詳しくは成形同時絵付法、即ちプラス
チツクス成形品の成形と同時に該成形品表面に図
柄を転写絵付する方法において使用することを可
能とした成形同時絵付用転写材に関するものであ
る。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a transfer material for painting at the same time as molding, and more specifically, a method for painting at the same time as molding, that is, a method for transferring and painting a design onto the surface of a plastic molded product at the same time as the molding. The present invention relates to a transfer material for painting at the same time as molding that can be used.
そして本発明の目的とするところは、プラスチ
ツクス成形品の所定の位置へ正確に図柄を転写絵
付することを可能とした成形同時絵付用転写材を
提供せもんとすることにある。 It is an object of the present invention to provide a transfer material for painting at the same time as molding, which makes it possible to accurately transfer and paint a design onto a predetermined position of a plastic molded product.
従来、プラスチツクス成形品表面に図柄を設け
る手段としては、予め成形された成形品の表面
に、スクリーン印刷法等によつて図柄を設ける所
謂成形後直接印刷方法、予め成形された成形品
の表面に、ホツトスタンピング箔を使用して、熱
と圧力により図柄を設ける所謂成形後転写印刷方
法、あるいは所望の図柄を印刷したシートを、
静電気力等により成形用金型内に仮着した後、成
形用樹脂を金型内に射出してプラスチツクス成形
品の成形と同時に該シートを融着一体化する所謂
インサート成形方法等がある。 Conventionally, methods for providing designs on the surface of plastic molded products include the so-called post-molding direct printing method, in which designs are printed on the surface of a pre-formed molded product by screen printing, etc.; The so-called post-forming transfer printing method uses hot stamping foil to create a design using heat and pressure, or a sheet with a desired design printed on it.
There is a so-called insert molding method in which the sheet is temporarily attached in a molding die by electrostatic force or the like, and then a molding resin is injected into the mold to fuse and integrate the sheet simultaneously with the molding of a plastic molded product.
しかしながら前記した方法は、何れも次のよう
な欠点を有するものである。即ち、の成形後直
接印刷方法の場合には、乾燥速度の遅い溶剤を含
むインキを用いねばならないため、印刷後直ちに
成形品を積み重ねる等の取扱が出来ないばかりで
なく、印刷後にインキを乾燥させる工程が必要で
あり、また成形用樹脂の種類によつてはインキ中
の溶剤の為に成形品表面にひび割れ等を起こし易
く、またの成形後転写印刷方法の場合には、成
形工程と転写印刷工程との2工程を必要とするも
のであり、またのインサート成形方法の場合に
は、金型内の所定の位置に正確にシートを仮着す
るのが極めて困難であり、得られた成形品表面の
図柄に位置ズレを生じ易いばかりでなく、シート
を成形品に融着せしめるものであるから、開孔部
を有する成形品に対しては適用不可能なものであ
る等、各々大きな欠点を有するものである。更に
前記した方法は何れも単純な平面や二次曲面を呈
する成形品にしか図柄を施すことが出来ず、微細
な凹凸部や曲面部を有する立体形状の成形品に対
しては適用不可能なものである。 However, all of the above methods have the following drawbacks. That is, in the case of the direct printing method after molding, it is necessary to use ink containing a solvent that has a slow drying rate, so not only is it impossible to stack the molded products immediately after printing, but also the ink must be dried after printing. Depending on the type of molding resin, the solvent in the ink can easily cause cracks on the surface of the molded product, and in the case of the post-molding transfer printing method, the molding process and transfer printing In addition, in the case of the insert molding method, it is extremely difficult to temporarily attach the sheet to the predetermined position in the mold, and the resulting molded product Each method has major drawbacks, such as not only the pattern on the surface being easily misaligned, but also the fact that the sheet is fused to the molded product, so it cannot be applied to molded products with holes. It is something that you have. Furthermore, all of the methods described above can only apply designs to molded products that have a simple plane or quadratic curved surface, and cannot be applied to three-dimensional molded products that have minute irregularities or curved surfaces. It is something.
一方、成形品に図柄を設ける他の手段として例
えば特開昭48−43760号公報、特開昭49−105856
号公報、特開昭56−151596号公報、特開昭57−
195683号公報等に示す方法が公知である。これら
は成形と同時に転写印刷を行う方法を示したので
あり、前記した3つの方法と異なり凹凸部や曲面
部を呈する立体形状の成型品に対しても適用可能
なものである。 On the other hand, as other means for providing designs on molded products, for example, JP-A-48-43760, JP-A-49-105856
Publication No. 151596, Japanese Patent Application Publication No. 151596, Japanese Patent Application Publication No. 1987-
A method disclosed in Japanese Patent No. 195683 is known. These methods show a method of performing transfer printing at the same time as molding, and unlike the three methods described above, these methods can also be applied to three-dimensional molded products exhibiting uneven portions and curved surfaces.
しかしながらこれらの公報に示される技術は何
れも凹凸部や曲面部を呈する立体形状の成型品表
面に如何に図柄を形成するかという技術的課題を
解決せんとして発明されたに過ぎないものであ
る。この点について更に詳しく述べれば、例えば
特開昭48−43760号公報や特開昭49−105856号公
報は単に成型と同時に金型内で転写印刷を行うた
めの方法を示したものであり、従つて転写材の基
体シートの選択並びに層構成に対する知見に乏し
いものである。また、特開昭56−151596号公報や
特開昭57−195683号公報にはより段差の大きい複
雑な曲面を呈する立体成形品に対して転写印刷を
可能とする方法が示されており、即ち、転写材の
基体シートとして伸び率の大なるプラスチツクス
フイルムを使用し、場合によつては射出成形前に
転写材を加熱し射出成形時に金型内で転写材全体
が伸び易い状態にして成形を行う等の方法が述べ
られている。つまり、より凹凸段差の大きい複雑
な曲面を呈する立体形状の成形品に対する対応と
しての考え方を示したものである。 However, the techniques disclosed in these publications were merely invented to solve the technical problem of how to form a pattern on the surface of a three-dimensional molded product exhibiting uneven parts and curved parts. To explain this point in more detail, for example, JP-A-48-43760 and JP-A-49-105856 simply show a method for performing transfer printing within a mold at the same time as molding. Therefore, there is a lack of knowledge regarding the selection of the base sheet of the transfer material and the layer structure. In addition, Japanese Patent Application Laid-Open Nos. 56-151596 and 1987-195683 disclose methods that enable transfer printing on three-dimensional molded products that have complex curved surfaces with larger steps. , a plastic film with a high elongation rate is used as the base sheet of the transfer material, and in some cases, the transfer material is heated before injection molding so that the entire transfer material is easily stretched in the mold during injection molding. It describes how to do this. In other words, this is a concept that can be applied to three-dimensional molded products that exhibit complex curved surfaces with larger unevenness and steps.
而るに従来の成形と同時に転写印刷を行う方法
に関する技術は何れもより凹凸段差の大きい立体
形状の成形品に対する絵付技術に関する研究であ
り立体形状の成形品の所定の位置に対し如何に正
確に位置決めされた図柄を形成するかという技術
的課題を解決せんとして発明されたものではな
く、従つて精度の高い図柄位置合わせを目的とし
た成形同時転写絵付技術の研究は現在に至る迄全
く成されていないのが実情である。 However, the technology related to the method of performing transfer printing at the same time as conventional molding is a research on painting techniques for three-dimensional molded products with large unevenness, and it is difficult to accurately place a predetermined position on a three-dimensional molded product. It was not invented to solve the technical problem of how to form a positioned pattern; therefore, no research has been conducted to date on molding and simultaneous transfer painting technology for the purpose of highly accurate pattern alignment. The reality is that it is not.
そこで本発明者は前記した種々の問題点を解消
すべく、更にはこれまで全く注目されていなかつ
た見地より成形同時転写絵付技術について鋭意研
究、実験の結果、遂に本発明を完成するに至つた
ものである。即ち、本発明は、基体シート上に転
写層を形成してなる成形同時絵付用転写材におい
て、基体シートが、転写材製造工程における熱と
張力に対しては伸縮性を示さず射出成形工程にお
ける溶融樹脂の熱量と射出圧力に対しては可塑性
を示すプラスチツクスフイルムであることを特徴
とする成形同時絵付用転写材である。 Therefore, in order to solve the various problems mentioned above, the inventor of the present invention has finally completed the present invention as a result of intensive research and experiments on molding simultaneous transfer painting technology from a viewpoint that has not received any attention up to now. It is something. That is, the present invention provides a transfer material for simultaneous molding and painting in which a transfer layer is formed on a base sheet, in which the base sheet does not exhibit elasticity with respect to heat and tension in the transfer material manufacturing process and does not exhibit elasticity in the injection molding process. This is a transfer material for painting at the same time as molding, which is characterized by being a plastic film that exhibits plasticity with respect to the heat quantity and injection pressure of the molten resin.
以下、本発明に係る成形同時絵付用転写材につ
いて図面を用いて更に詳しく説明する。 Hereinafter, the transfer material for decorating while molding according to the present invention will be explained in more detail with reference to the drawings.
本発明に係る転写材1は、基体シート2上に図
柄層3、接着剤層4等の転写層5を形成してなる
ものである(第1図参照)。 The transfer material 1 according to the present invention is formed by forming a transfer layer 5 such as a pattern layer 3 and an adhesive layer 4 on a base sheet 2 (see FIG. 1).
本発明において使用する基体シート2は、転写
材製造工程における熱と張力、及び射出成形工程
における転写材1をセツトする際の張力に対して
は伸縮性を示さず且つ射出成形工程における溶融
樹脂の熱量と射出圧力に対しては可塑性を示すプ
ラスチツクスフイルムである。即ち、転写材の製
造工程において転写材の各層を印刷する際と乾燥
する際、及び射出成形工程において該転写材をセ
ツトする際には寸法安定性に極めて優れ、高精度
な位置合わせが可能なものであり、成形用樹脂が
キヤビテイー部に射出された時、凹凸の立ち上が
り部やR部(面と面との境界線)のように転写材
の伸びが強要される部分においては伸びが発生す
るようなプラスチツクスフイルムである。このよ
うなプラスチツクスフイルムとしては二軸延伸ポ
リエステルフイルム及び二軸延伸ナイロンフイル
ム、或いは二軸延伸ポリエステルフイルムと二軸
延伸ナイロンフイルムとのラミネートフイルム等
がある。本発明において前記したような基体シー
ト2を用いるのは次のような理由によるものであ
る。即ち、通常、成形同時絵付用転写材の基体シ
ートは、立体形状の成形品表面の凹凸部や曲面部
に出来るだけ沿うようにするために伸縮性に優れ
たプラスチツクスフイルム、例えば無延伸ポリエ
ステルフイルム、無延伸ナイロンフイルムあるい
はポリ塩化ビニルフイルム等が用いられるもので
あるが、このようなプラスチツクスフイルムは、
引張力に対する機械的強度が弱いため容易に変形
を起こし、また耐熱性も低いため寸法安定性に劣
り、印刷工程において精密な見当図柄を印刷する
ことが難しいだけでなく射出成形時においても成
形用樹脂の流れに沿つて基体シート自体が全体に
変形を起こし易く図柄の変形が生ずるものであ
り、特にウエルドラインの発生する箇所では基体
シートの変形が集中しシワの発生という問題を有
し、前記した伸び易い性質が逆に欠点となつて現
れることが明らかとなつたからである。 The base sheet 2 used in the present invention does not show elasticity against the heat and tension in the transfer material manufacturing process and the tension when setting the transfer material 1 in the injection molding process, and does not show elasticity against the heat and tension in the transfer material manufacturing process and the tension when setting the transfer material 1 in the injection molding process. It is a plastic film that shows plasticity with respect to heat and injection pressure. In other words, when printing and drying each layer of the transfer material in the transfer material manufacturing process, and when setting the transfer material in the injection molding process, it has excellent dimensional stability and enables highly accurate positioning. When molding resin is injected into the cavity, elongation occurs in areas where the transfer material is forced to elongate, such as the rising edges of irregularities and the R portion (boundary line between surfaces). It's like a plastic film. Examples of such plastic films include biaxially oriented polyester films, biaxially oriented nylon films, and laminate films of biaxially oriented polyester films and biaxially oriented nylon films. The reason why the base sheet 2 as described above is used in the present invention is as follows. That is, the base sheet of the transfer material for painting at the same time as molding is usually a plastic film with excellent elasticity, such as an unstretched polyester film, in order to conform as much as possible to the irregularities and curved surfaces of the surface of the three-dimensional molded product. , unstretched nylon film or polyvinyl chloride film, etc.;
It easily deforms due to its weak mechanical strength against tensile force, and has poor dimensional stability due to its low heat resistance, making it difficult not only to print precise register patterns in the printing process but also to prevent molding during injection molding. The base sheet itself is easily deformed as a whole along the resin flow, resulting in deformation of the design, and the deformation of the base sheet is particularly concentrated in areas where weld lines occur, causing the problem of wrinkles. This is because it has become clear that the easy-to-stretch property actually appears as a drawback.
なお、本発明の転写材1に使用する基体シート
2の厚さについては成形品の形状によつて選択さ
れるべきであるが使用範囲としては20〜100μm程
度であり好ましくは25〜75μmの範囲が好適であ
る。 The thickness of the base sheet 2 used in the transfer material 1 of the present invention should be selected depending on the shape of the molded product, but the usable range is about 20 to 100 μm, preferably 25 to 75 μm. is suitable.
本発明に係る成形同時絵付用転写材1において
重要な点は、前記した基体シート2を使用するこ
とであるが、本発明の目的をより大きく達成する
ために、前記基体シート2上に、次に述べる融着
防止層6を設けることができる。この融着防止層
6は、前記基体シート2が射出成形時に可塑性を
示し、引き延ばされる部分において該基体シート
2と転写層5とが融着するのを防止するための層
である。即ち、この融着防止層6は、これを設け
ない場合、射出成形時、凹凸の立ち上がり部やR
部のように転写材1の伸びが強要される部分にお
いて基体シート2及び基体シート上に印刷された
層は著しく伸びが生じせしめられ、新しく活性化
された表面が現出することにより基体シート2と
転写層5とが融着することがあり(第2−a図及
び第2−b図参照)、このようなことを防止する
ために、本発明においては融着防子層6を形成す
るものである。 An important point in the transfer material 1 for simultaneous molding and painting according to the present invention is the use of the base sheet 2 described above. The anti-fusing layer 6 described in 2 can be provided. This anti-fusing layer 6 is a layer for preventing the base sheet 2 and the transfer layer 5 from being fused together in the portion where the base sheet 2 exhibits plasticity during injection molding and is stretched. That is, if this anti-fusing layer 6 is not provided, the uneven rising portions and R
In the areas where the transfer material 1 is forced to elongate, the base sheet 2 and the layer printed on the base sheet are significantly stretched, and a newly activated surface appears, causing the base sheet 2 to elongate. The transfer layer 5 and the transfer layer 5 may be fused together (see Figures 2-a and 2-b), and in order to prevent this, in the present invention, a fusion protection layer 6 is formed. It is something.
この融着防止層6に使用することができる材料
は、架橋することにより硬化する樹脂、即ち熱に
対して極めて安定で不活性表面を形成するような
樹脂であり、このようなものとしては硬化性樹
脂、例えばメラミン系樹脂、尿素系樹脂、ベンゾ
グアナミン系樹脂、エポキシ系樹脂、熱硬化アク
リル系樹脂、ウレタン系樹脂、ポリエステル系樹
脂、アルキツド系樹脂などの熱硬化性樹脂、ある
いは二液硬化性樹脂、その他に紫外線や電子線の
照射により架橋硬化するように設計されたアクリ
ル系樹脂、ウレタン樹脂、アクリルウレタン系樹
脂、エポキシ系樹脂をベースとする紫外線硬化型
樹脂、電子線硬化型樹脂などがある。融着防止層
6として前記したような樹脂を用いるのは、該融
着防止層6は射出成形時金型内において凹凸の立
ち上がり部やR部等の転写材の伸びが強要される
部分において基体シートの伸びに追随出来ずクラ
ツクを発生するにもかかわらず、そのクラツクは
非常に細かなものであり且つその表面は不活性な
表面であるから融着防止効果を維持するというこ
とが本発明者による多数の実験例から見い出され
たからである(第3−a図及び第3−b図参照)、
これら硬化性樹脂の実際の使用に際しては硬化性
樹脂の単独あるいは2種以上の混合物にコーテイ
ング適性を配慮して適宜融着防止機能を損なわな
い範囲内で熱可塑性樹脂を配合して用いるとよ
い。また微粉末シリカ、タルク、クレー、炭酸カ
ルシウム、沈降性硫酸バリウム等の無機質充填剤
を配合することによつて成形品表面を艶消し状態
に仕上げることもできる。融着防止層6を設ける
手段としてはグラビアコーテイング、バーコーテ
イング等の塗布方法があり、通常は図柄層3の印
刷に先立つて別工程にて行われる。 The material that can be used for this anti-fusing layer 6 is a resin that hardens by crosslinking, that is, a resin that is extremely stable against heat and forms an inert surface. thermosetting resins such as melamine resins, urea resins, benzoguanamine resins, epoxy resins, thermosetting acrylic resins, urethane resins, polyester resins, alkyd resins, or two-component curable resins. In addition, there are acrylic resins, urethane resins, acrylic urethane resins, ultraviolet curable resins based on epoxy resins, and electron beam curable resins designed to be cross-linked and cured by irradiation with ultraviolet rays or electron beams. . The reason why the above-mentioned resin is used as the anti-fusion layer 6 is that the anti-fusion layer 6 is applied to the substrate in areas where the elongation of the transfer material is forced, such as the raised areas of unevenness and R areas in the mold during injection molding. The inventor of the present invention found that although cracks occur due to the inability to follow the elongation of the sheet, the cracks are very small and the surface is inert, so the anti-fusing effect is maintained. This is because it was discovered from numerous experimental examples by (see Figures 3-a and 3-b),
When these curable resins are actually used, it is preferable to mix thermoplastic resins with the curable resins alone or in a mixture of two or more of them, taking into account suitability for coating, within a range that does not impair the anti-fusion function. Furthermore, the surface of the molded product can be finished in a matte state by blending an inorganic filler such as finely powdered silica, talc, clay, calcium carbonate, or precipitated barium sulfate. There are coating methods such as gravure coating and bar coating as means for providing the anti-fusion layer 6, and this is usually carried out in a separate process prior to printing the pattern layer 3.
本発明に係る成形同時絵付用転写材1は前記し
た基体シート2及び融着防止層6が形成された基
体シート2上に、適宜離型保護層7、図柄層3、
接着剤層4等が設けられるものである。 The transfer material 1 for painting at the same time as molding according to the present invention is provided on the base sheet 2 on which the above-described base sheet 2 and anti-fusing layer 6 are formed, a mold release protective layer 7, a pattern layer 3,
An adhesive layer 4 and the like are provided.
以下、順次離型保護層7、図柄層3、接着剤層
4について説明する。 The release protective layer 7, the pattern layer 3, and the adhesive layer 4 will be explained in this order below.
先ず離型保護層7は射出成形工程後、基体シー
ト2と転写層5とを容易に剥離させるためのもの
である。この離型保護層7に使用することができ
る材料としては熱可塑アクリル樹脂、繊維素系樹
脂、塩化ビニル・酢酸ビニル共重合樹脂、熱可塑
性ポリエステル樹脂、熱可塑ウレタン樹脂、塩化
ゴム、塩素化ポリオレフイン系樹脂などの熱可塑
性樹脂を主成分とし更に着色剤、可塑剤、皮膜強
化剤、紫外線吸収剤等の配合剤を加えた組成物を
使用することができる。 First, the mold release protective layer 7 is for easily separating the base sheet 2 and the transfer layer 5 after the injection molding process. Materials that can be used for the mold release protective layer 7 include thermoplastic acrylic resin, cellulose resin, vinyl chloride/vinyl acetate copolymer resin, thermoplastic polyester resin, thermoplastic urethane resin, chlorinated rubber, and chlorinated polyolefin. A composition containing a thermoplastic resin such as a thermoplastic resin as a main component and further additives such as a coloring agent, a plasticizer, a film strengthening agent, and an ultraviolet absorber can be used.
なお、前記離型保護層7は射出成形工程後、成
形物の表面となるものであるから、耐摩耗性、耐
キズ性、耐薬品性等の諸特性が要求されるもので
ある。 Since the mold release protective layer 7 becomes the surface of the molded product after the injection molding process, it is required to have various properties such as wear resistance, scratch resistance, and chemical resistance.
次に図柄層3は前記離型保護層7上に、離型保
護層7を設けない場合は前記融着防止層6上に設
けられる。この図柄層3に使用する材料としては
熱可塑性アクリル樹脂、繊維素系樹脂、塩化ビニ
ル・酢酸ビニル共重合樹脂、熱可塑ウレタン樹
脂、塩化ゴム、塩素化ポリオレフイン系樹脂、熱
可塑性ポリエステル樹脂、ポリアミド系樹脂、石
油樹脂、天然樹脂等の熱可塑性樹脂の1種または
2種以上からなるバインダーと酸化チタン、カー
ボンブラツク、弁柄等の無機顔料及びフタロシア
ニン系、アゾ系、アントラキノン系、トリフエニ
ルメタン系染顔料、キナクリドン系樹脂、ジオキ
サジン系顔料等の有機系色素と適宜これらに分散
剤、消泡剤、可塑剤等の助剤を配合してなる組成
物を使用することができる。 Next, the pattern layer 3 is provided on the release protection layer 7, or on the fusion prevention layer 6 if the release protection layer 7 is not provided. Materials used for this pattern layer 3 include thermoplastic acrylic resin, cellulose resin, vinyl chloride/vinyl acetate copolymer resin, thermoplastic urethane resin, chlorinated rubber, chlorinated polyolefin resin, thermoplastic polyester resin, and polyamide resin. A binder made of one or more thermoplastic resins such as resins, petroleum resins, and natural resins, inorganic pigments such as titanium oxide, carbon black, and Bengara, and phthalocyanine, azo, anthraquinone, and triphenylmethane dyes. It is possible to use a composition comprising organic dyes such as pigments, quinacridone resins, and dioxazine pigments, and auxiliary agents such as dispersants, antifoaming agents, and plasticizers.
更に接着剤層4は前記図柄層3上に設けられ
る。この接着剤層4に使用する材料としては射出
成形時に使用される成形用樹脂の溶融温度よりも
軟化点が低く、成形用樹脂との相溶性もあり結果
として成形用樹脂に対して熱接着可能なものであ
ることが必要である。このようなものとしては例
えばABS樹脂、スチロール樹脂、熱可塑アクリ
ル樹脂、ポリカーボネート、繊維素系樹脂、塩化
ビニル・酢酸ビニル共重合樹脂、ポリアミド系樹
脂、ポリエステル樹脂、環化ゴム、塩素化ポリオ
レフイン、石油樹脂、天然樹脂等を主成分とし、
必要に応じて前記図柄層3に使用するインキ組成
物と同様に各種着色剤、助剤を配合してもよい。 Furthermore, an adhesive layer 4 is provided on the pattern layer 3. The material used for this adhesive layer 4 has a softening point lower than the melting temperature of the molding resin used during injection molding, and is compatible with the molding resin, so it can be thermally bonded to the molding resin. It is necessary that the Examples of such materials include ABS resin, styrene resin, thermoplastic acrylic resin, polycarbonate, cellulose resin, vinyl chloride/vinyl acetate copolymer resin, polyamide resin, polyester resin, cyclized rubber, chlorinated polyolefin, and petroleum. Main ingredients include resin, natural resin, etc.
If necessary, various coloring agents and auxiliary agents may be blended in the same manner as in the ink composition used for the pattern layer 3.
本発明に係る成形同時絵付用転写材は以上の構
成からなるものである。この転写材の使用に当た
つては例えば先ず射出成形機に取りつけられた転
写材送り装置に図柄を印刷した長尺の転写材を設
置し、次に射出成形用金型の雄型・雌型の間に該
転写材を接着剤層が金型のゲート部に向くように
送り込み、各成形サイクル毎に成形品に対応する
金型内のキヤビテイー部に対して正確に位置決め
を行つた後該金型を閉じ、その後溶融した成形用
樹脂をキヤビテイー部に射出し、冷却後該金型の
型開き動作を利用して基体シートを剥離する。こ
のようにすることによつて図柄が転写絵付された
成形品を得ることができる。 The transfer material for painting while molding according to the present invention has the above-described structure. When using this transfer material, for example, first, a long transfer material with a pattern printed on it is installed in the transfer material feeding device attached to the injection molding machine, and then the male and female molds of the injection mold are placed. During each molding cycle, the transfer material is fed so that the adhesive layer faces the gate part of the mold, and after accurately positioning it with respect to the cavity part in the mold corresponding to the molded product, the mold is The mold is closed, and then molten molding resin is injected into the cavity, and after cooling, the base sheet is peeled off using the mold opening action of the mold. By doing so, it is possible to obtain a molded article with a transferred design.
次に具体的に実施例を挙げ、説明する。但し
「部」は全て「重量部」を表す。 Next, specific examples will be given and explained. However, all "parts" represent "parts by weight."
<実施例 1>
コロナ放電処理を施した二軸延伸ポリエステル
フイルム#50上に下記の組成からなるインキを
用いグラビアコート法にて厚さ2μmの融着防止層
を形成し、180℃の雰囲気温度にて20秒間硬化処
理した後、その上に下記の組成からなるインキ
を用いてグラビア印刷法にて離型保護層を形成
し、その上に下記の組成からなるインキを用い
てグラビア印刷法にて4色見当を合わせた図柄層
を形成し、更にその上に下記の組成からなるイ
ンキを用いて同じくグラビアコート法にて接着剤
層を形成した。<Example 1> An anti-fusion layer with a thickness of 2 μm was formed by gravure coating using an ink having the composition below on biaxially stretched polyester film #50 that had been subjected to corona discharge treatment, and the film was heated at an ambient temperature of 180°C. After curing for 20 seconds in A pattern layer having four colors in register was formed thereon, and an adhesive layer was further formed thereon by the same gravure coating method using ink having the composition shown below.
メラミン樹脂 80部
エポキシ樹脂 20部
トルエン/MEK(メチルエチルケトン)=1/
1 200部
熱可塑アクリル系樹脂 70部
塩化ビニル・酢酸ビニル共重合樹脂 30部
ポリエチレンワツクス 3部
トルエン/MEK=1/1 200部
熱可塑アクリル系樹脂 30部
塩化ゴム 30部
顔料 30部
塩化パラフイン 5部
界面活性剤 0.5部
トルエン/酢酸エチル=3/7 260部
スチレン樹脂 20部
トルエン/酢酸エチル=1/1 80部
上記した構成からなる転写材を射出成形機にセ
ツトし位置決めを行つた後金型を閉じ200℃に溶
融したスチロール樹脂をキヤビテイー部に射出し
冷却後金型を開け融着防止層が固着した基体シー
トを剥離して図柄が転写された成形品を得た。こ
の成形品の形状は高さ4mm、角のR(半径)が2
mm、1辺50mm、他辺150mm、樹脂の厚み1.5mmの四
角形型のリモコンスイツチのパネルであり目盛盤
が形成されたものである。成形後この目盛盤の目
盛位置を測定してみると成形品の所定位置に対し
て±0.1mmの位置精度で転写されており、コーナ
部、側面部にも図柄が美麗に転写されたものであ
つた。 Melamine resin 80 parts Epoxy resin 20 parts Toluene/MEK (methyl ethyl ketone) = 1/
1 200 parts Thermoplastic acrylic resin 70 parts Vinyl chloride/vinyl acetate copolymer resin 30 parts Polyethylene wax 3 parts Toluene/MEK=1/1 200 parts Thermoplastic acrylic resin 30 parts Chlorinated rubber 30 parts Pigment 30 parts Chlorinated paraffin 5 parts Surfactant 0.5 parts Toluene/ethyl acetate = 3/7 260 parts Styrene resin 20 parts Toluene/ethyl acetate = 1/1 80 parts After setting the transfer material with the above structure in the injection molding machine and positioning it. The mold was closed, and styrene resin molten at 200°C was injected into the cavity. After cooling, the mold was opened and the base sheet to which the anti-fusing layer was adhered was peeled off to obtain a molded product with the pattern transferred thereon. The shape of this molded product has a height of 4 mm and a corner R (radius) of 2
It is a rectangular remote control switch panel with a diameter of 50 mm on one side, 150 mm on the other side, and a resin thickness of 1.5 mm, with a scale plate formed on it. After molding, we measured the scale position of this dial and found that it was transferred to the specified position of the molded product with a positional accuracy of ±0.1mm, and the design was also beautifully transferred to the corners and sides. It was hot.
<実施例 2>
コロナ放電処理されていない二軸延伸ポリエス
テルフイルム#25上に下記の組成からなるイン
キを用い融着防止層を形成し、その上に下記の
組成からなるインキを用い図柄層を形成し、更に
その上に下記の組成からなるインキを用い接着
剤層を形成した。<Example 2> On biaxially stretched polyester film #25 that has not been subjected to corona discharge treatment, a fusion prevention layer is formed using an ink having the following composition, and a pattern layer is formed on top of the anti-fusing layer using an ink having the following composition. An adhesive layer was formed thereon using an ink having the composition shown below.
尿素樹脂(尿素、ホルムアルデヒド縮合物)
60部
エポキシ樹脂 20部
CAB(セルロースアセテートブチレート)
20部
酸触媒(硬化剤) 5部
メタノール/MEK=4/1 200部
塩化ビニル・酢酸ビニル・マレイン酸共重合
樹脂
30部
熱可塑アクリル樹脂 70部
顔料 50部
アジピン酸エステル系可塑剤 10部
分散剤 0.3部
MIBK(メチルイソブチルケトン)/MEK=
1/1
200部
ABS樹脂 50部
石油樹脂 10部
顔料 20部
トルエン/酢酸エチル=3/7 200部
上記した構成からなる転写材を実施例1と同様
に射出成形機にセツトした後位置決めを行い、そ
の後金型を閉じ230℃に溶融したABS樹脂をキヤ
ビテイー部に射出し冷却後金型を開け基体シート
を剥離すると図柄が転写された成形品を得た。こ
の成形品の表面は融着防止層が現れており、その
形状は、樹脂の厚み2mm、平板状、パーテイング
ラインはトツプ面より1mm下、外周のR(半径)
は0.5mm、開孔部分の角のRは0.1mm、パーテイン
グラインはトツプ面より0.5mm下であるようなパ
ネルであり、実施例1と同様に位置精度を測定し
てみると、成形品の所定位置に対して±0.1mmの
位置精度で転写されており、コーナ部、側面部、
開孔部のコーナ部、側面部にも図柄が美麗に転写
されたものであつた。 Urea resin (urea, formaldehyde condensate) 60 parts Epoxy resin 20 parts CAB (cellulose acetate butyrate) 20 parts Acid catalyst (curing agent) 5 parts Methanol/MEK=4/1 200 parts Vinyl chloride, vinyl acetate, maleic acid Polymer resin 30 parts Thermoplastic acrylic resin 70 parts Pigment 50 parts Adipate ester plasticizer 10 parts Dispersant 0.3 parts MIBK (methyl isobutyl ketone)/MEK=
1/1 200 parts ABS resin 50 parts Petroleum resin 10 parts Pigment 20 parts Toluene/ethyl acetate = 3/7 200 parts The transfer material having the above structure was set in the injection molding machine in the same manner as in Example 1, and then positioned. Then, the mold was closed, ABS resin molten at 230°C was injected into the cavity, and after cooling, the mold was opened and the base sheet was peeled off to obtain a molded product with the pattern transferred. A fusion prevention layer appears on the surface of this molded product, and its shape is a flat plate with a resin thickness of 2 mm, the parting line is 1 mm below the top surface, and the R (radius) of the outer periphery.
is 0.5mm, the radius of the corner of the opening is 0.1mm, and the parting line is 0.5mm below the top surface.When we measured the positional accuracy in the same manner as in Example 1, we found that the molded product It is transferred with a positional accuracy of ±0.1mm to the specified position of the corner, side,
The design was also beautifully transferred to the corners and sides of the opening.
<実施例 3>
コロナ放電処理された二軸延伸ポリエステルフ
イルム#75上に下記の組成からなるインキを用
いて融着防止層をリバースコート法にて成形し、
150℃の雰囲気温度で20秒間硬化促進の乾燥後、
室温(約25℃)にて5日間放置した後(乾燥後の
塗膜の厚み3μm)、その上に実施例1と同様のイ
ンキを用いて離型保護層を形成し、その上に実
施例1と同様のインキを用いて図柄層を形成
し、更にその上に下記の組成からなるインキを
用いて接着剤層を形成した。<Example 3> An anti-fusing layer was formed on corona discharge treated biaxially oriented polyester film #75 using an ink having the following composition by a reverse coating method,
After drying at an ambient temperature of 150℃ for 20 seconds to accelerate curing,
After being left at room temperature (approximately 25°C) for 5 days (the thickness of the coating after drying is 3 μm), a release protective layer was formed thereon using the same ink as in Example 1, and then Example A pattern layer was formed using the same ink as in Example 1, and an adhesive layer was further formed thereon using an ink having the composition shown below.
ウレタン樹脂 90部
微粉末シリカ 10部
トルエン/酢酸エチル/酢酸ビニル=4/3/
3 200部
塩素化ポリプロピレン 20部
トルエン 80部
上記した構成からなる転写材を実施例1と同様
に射出成形機にセツトした後位置決めを行い、そ
の後金型を閉じ溶融したポリプロピレン樹脂をキ
ヤビテイー部に射出し冷却後金型を開け基体シー
トを剥離すると図柄が転写されたポリプロピレン
製洗濯機計器盤を得た。この計器盤の形状は300
mm×100mmの長方形で立上がり5mm、樹脂の厚み
2mm、外周のR(半径)は1.5mmであり、更に円
形・長方形等の開口部が17箇所有り、開口部のR
(半径)0.2mm〜2mm、パーテイングラインはトツ
プ面より0.3mm〜2mmの範囲であつた。実施例1
と同様に位置精度を測定してみると、成形品の所
定位置に対して±0.1mmの位置精度で転写されて
おり、コーナ部、側面部、開口部側面にも図柄が
美麗に転写されたものであつた。 Urethane resin 90 parts Finely powdered silica 10 parts Toluene/ethyl acetate/vinyl acetate = 4/3/
3 200 parts Chlorinated polypropylene 20 parts Toluene 80 parts The transfer material having the above structure was set in the injection molding machine and positioned in the same manner as in Example 1, and then the mold was closed and molten polypropylene resin was injected into the cavity. After cooling, the mold was opened and the base sheet was peeled off to obtain a polypropylene washing machine instrument panel with a transferred design. The shape of this instrument panel is 300
It is a rectangle of mm x 100mm with a rising edge of 5mm, a resin thickness of 2mm, and an outer circumference R (radius) of 1.5mm. Furthermore, there are 17 circular and rectangular openings, and the opening radius is 1.5mm.
(Radius) 0.2 mm to 2 mm, and the parting line ranged from 0.3 mm to 2 mm from the top surface. Example 1
When we measured the positional accuracy in the same way as above, we found that the pattern was transferred with a positional accuracy of ±0.1mm to the specified position on the molded product, and the design was also beautifully transferred to the corners, sides, and sides of the opening. It was hot.
<比較例>
コロナ放電処理を施した無延伸ポリエステルフ
イルム#50上に実施例1と同様の組成からなる図
柄層及び接着剤層を形成してなる転写材を用い、
他は実施例1と同様に行つた。<Comparative Example> Using a transfer material in which a pattern layer and an adhesive layer having the same composition as in Example 1 were formed on unstretched polyester film #50 that had been subjected to corona discharge treatment,
The rest was carried out in the same manner as in Example 1.
多色印刷工程において各色毎の見当が合いにく
かつ転写材の図柄寸法を測定すると原稿寸法100
mmに対して±0.5mm以上の伸縮があつた。更に成
形後、目盛盤の目盛位置を測定してみると成形品
の所定の位置に対して±0.5mm以上の位置ズレが
みられた。 In the multicolor printing process, the registration of each color is difficult to match, and when measuring the design size of the transfer material, the original size is 100.
There was expansion and contraction of ±0.5 mm or more with respect to mm. Furthermore, when the scale position of the scale plate was measured after molding, it was found that there was a positional deviation of ±0.5 mm or more from the predetermined position of the molded product.
第1図は本発明に係る転写材の一実施例を示す
断面模式図、第2−a図は従来の転写材を用いて
射出成形を行つた場合のR部寸近の断面模式図、
第2−b図は従来の転写材を用いて射出成形を行
つた場合の剥離後の基体シートの断面模式図、第
3−a図は本発明に係る転写材を用いて射出成形
を行つた場合のR部付近の断面模式図、第3−b
図は本発明に係る転写材を用いて射出成形を行つ
た場合の剥離後の基体シートの断面模式図を各々
示す。
図中、1……転写材、2……基体シート、3…
…図柄層、4……接着剤層、5……転写層、6…
…融着防止層、7……離型保護層、8……成形
品。
FIG. 1 is a schematic cross-sectional view showing an embodiment of the transfer material according to the present invention, FIG.
Figure 2-b is a schematic cross-sectional view of the base sheet after peeling when injection molding is performed using a conventional transfer material, and Figure 3-a is a schematic cross-sectional view of the base sheet when injection molding is performed using the transfer material according to the present invention. Schematic cross-sectional diagram near the R part in case 3-b
The figures each show a schematic cross-sectional view of the base sheet after peeling when injection molding is performed using the transfer material according to the present invention. In the figure, 1... transfer material, 2... base sheet, 3...
...Design layer, 4...Adhesive layer, 5...Transfer layer, 6...
...Fusion prevention layer, 7... Mold release protective layer, 8... Molded article.
Claims (1)
時絵付用転写材において、基体シートが、転写材
製造工程における熱と張力に対しては伸縮性を示
さず射出成形工程における溶融樹脂の熱量と射出
圧力に対しては可塑性を示すプラスチツクスフイ
ルムであることを特徴とする成形同時絵付用転写
材。 2 基体シートが、二軸延伸プラスチツクスフイ
ルムであることを特徴とする特許請求の範囲第1
項記載の成形同時絵付用転写材。 3 基体シートが、転写材製造工程における熱と
張力に対しては伸縮性を示さず射出成形工程にお
ける溶融樹脂の熱量と射出圧力に対しては可塑性
を示すプラスチツクスフイルム上に、融着防止層
を形成したものであることを特徴とする特許請求
の範囲第1項記載の成形同時絵付用転写材。 4 基体シートが、二軸延伸プラスチツクスフイ
ルム上に融着防止層を形成したものであることを
特徴とする特許請求の範囲第3項記載の成形同時
絵付用転写材。[Scope of Claims] 1. In a transfer material for simultaneous molding and painting in which a transfer layer is formed on a base sheet, the base sheet does not exhibit elasticity against heat and tension during the transfer material manufacturing process, and does not exhibit elasticity during the injection molding process. A transfer material for painting at the same time as molding, characterized in that it is a plastic film that exhibits plasticity with respect to the heat quantity and injection pressure of the molten resin. 2. Claim 1, wherein the base sheet is a biaxially stretched plastic film.
Transfer material for painting at the same time as molding as described in section. 3 The base sheet is a plastic film that does not show elasticity against the heat and tension in the transfer material manufacturing process, but shows plasticity against the heat amount and injection pressure of the molten resin in the injection molding process, and an anti-fusing layer is formed on the plastic film. A transfer material for painting at the same time as claimed in claim 1, characterized in that the transfer material is formed by: 4. The transfer material for painting while molding as set forth in claim 3, wherein the base sheet is a biaxially stretched plastic film on which a fusion prevention layer is formed.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP9606583A JPS59220400A (en) | 1983-05-31 | 1983-05-31 | Transfer material for molding and painting at same time |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP9606583A JPS59220400A (en) | 1983-05-31 | 1983-05-31 | Transfer material for molding and painting at same time |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS59220400A JPS59220400A (en) | 1984-12-11 |
| JPH0242080B2 true JPH0242080B2 (en) | 1990-09-20 |
Family
ID=14155020
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP9606583A Granted JPS59220400A (en) | 1983-05-31 | 1983-05-31 | Transfer material for molding and painting at same time |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS59220400A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0776750A1 (en) | 1995-11-29 | 1997-06-04 | Dai Nippon Printing Co., Ltd. | Foil decorating injection molding machine |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0698874B2 (en) * | 1985-06-26 | 1994-12-07 | 日本写真印刷株式会社 | Transfer material |
| JPH0521437Y2 (en) * | 1985-07-19 | 1993-06-01 | ||
| JPS62175996U (en) * | 1986-04-28 | 1987-11-09 | ||
| JP2524254Y2 (en) * | 1994-05-30 | 1997-01-29 | 大日本印刷株式会社 | Thermal transfer sheet |
| JPH09123694A (en) * | 1995-10-31 | 1997-05-13 | Nissha Printing Co Ltd | Manufacture of stereoscopic pattern-transferred article and transfer material to be used for its manufacture |
-
1983
- 1983-05-31 JP JP9606583A patent/JPS59220400A/en active Granted
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0776750A1 (en) | 1995-11-29 | 1997-06-04 | Dai Nippon Printing Co., Ltd. | Foil decorating injection molding machine |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS59220400A (en) | 1984-12-11 |
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