JPH01147054A - Metallic vapor deposited transcribing film and its production - Google Patents
Metallic vapor deposited transcribing film and its productionInfo
- Publication number
- JPH01147054A JPH01147054A JP19706287A JP19706287A JPH01147054A JP H01147054 A JPH01147054 A JP H01147054A JP 19706287 A JP19706287 A JP 19706287A JP 19706287 A JP19706287 A JP 19706287A JP H01147054 A JPH01147054 A JP H01147054A
- Authority
- JP
- Japan
- Prior art keywords
- resin
- film
- layer
- metal vapor
- vapor deposited
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 4
- 229920005989 resin Polymers 0.000 claims abstract description 53
- 239000011347 resin Substances 0.000 claims abstract description 53
- 229910052751 metal Inorganic materials 0.000 claims abstract description 32
- 239000002184 metal Substances 0.000 claims abstract description 32
- 238000012546 transfer Methods 0.000 claims abstract description 26
- 238000007740 vapor deposition Methods 0.000 claims abstract description 22
- 239000007787 solid Substances 0.000 claims abstract description 13
- 239000002966 varnish Substances 0.000 claims abstract description 10
- 239000011248 coating agent Substances 0.000 claims description 9
- 230000008018 melting Effects 0.000 claims 2
- 238000002844 melting Methods 0.000 claims 2
- 230000001070 adhesive effect Effects 0.000 abstract description 8
- 239000000853 adhesive Substances 0.000 abstract description 7
- 239000003795 chemical substances by application Substances 0.000 abstract description 7
- 239000000463 material Substances 0.000 abstract description 6
- 238000000151 deposition Methods 0.000 abstract description 4
- 239000005038 ethylene vinyl acetate Substances 0.000 abstract description 4
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 abstract description 4
- 239000000020 Nitrocellulose Substances 0.000 abstract description 3
- 229920001220 nitrocellulos Polymers 0.000 abstract description 3
- 239000010408 film Substances 0.000 description 41
- 239000010410 layer Substances 0.000 description 18
- 238000000034 method Methods 0.000 description 11
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 9
- -1 etc.) Substances 0.000 description 7
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 6
- 229910052782 aluminium Inorganic materials 0.000 description 6
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 6
- 238000005260 corrosion Methods 0.000 description 6
- 230000007797 corrosion Effects 0.000 description 6
- 239000000123 paper Substances 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- 238000000576 coating method Methods 0.000 description 4
- 238000012545 processing Methods 0.000 description 4
- 229920000178 Acrylic resin Polymers 0.000 description 3
- 239000004925 Acrylic resin Substances 0.000 description 3
- 229920000298 Cellophane Polymers 0.000 description 3
- 239000004698 Polyethylene Substances 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 230000008021 deposition Effects 0.000 description 3
- 238000007645 offset printing Methods 0.000 description 3
- 229920000573 polyethylene Polymers 0.000 description 3
- 238000007639 printing Methods 0.000 description 3
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- 239000004743 Polypropylene Substances 0.000 description 2
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 2
- 239000012790 adhesive layer Substances 0.000 description 2
- 238000005452 bending Methods 0.000 description 2
- 229920006378 biaxially oriented polypropylene Polymers 0.000 description 2
- 239000011127 biaxially oriented polypropylene Substances 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 229920006226 ethylene-acrylic acid Polymers 0.000 description 2
- 239000004744 fabric Substances 0.000 description 2
- 238000012812 general test Methods 0.000 description 2
- 239000002655 kraft paper Substances 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 238000000465 moulding Methods 0.000 description 2
- 239000003973 paint Substances 0.000 description 2
- 239000005011 phenolic resin Substances 0.000 description 2
- 229920006267 polyester film Polymers 0.000 description 2
- 229920001155 polypropylene Polymers 0.000 description 2
- 229920005749 polyurethane resin Polymers 0.000 description 2
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 2
- 238000011179 visual inspection Methods 0.000 description 2
- 241000239290 Araneae Species 0.000 description 1
- 235000017166 Bambusa arundinacea Nutrition 0.000 description 1
- 235000017491 Bambusa tulda Nutrition 0.000 description 1
- 241001330002 Bambuseae Species 0.000 description 1
- 235000015334 Phyllostachys viridis Nutrition 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- 241000519995 Stachys sylvatica Species 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 229920006271 aliphatic hydrocarbon resin Polymers 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 229920006272 aromatic hydrocarbon resin Polymers 0.000 description 1
- 239000011425 bamboo Substances 0.000 description 1
- DQXBYHZEEUGOBF-UHFFFAOYSA-N but-3-enoic acid;ethene Chemical compound C=C.OC(=O)CC=C DQXBYHZEEUGOBF-UHFFFAOYSA-N 0.000 description 1
- 229920002301 cellulose acetate Polymers 0.000 description 1
- 229920006217 cellulose acetate butyrate Polymers 0.000 description 1
- 229920006026 co-polymeric resin Polymers 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 239000012792 core layer Substances 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000007765 extrusion coating Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 239000002932 luster Substances 0.000 description 1
- 239000011104 metalized film Substances 0.000 description 1
- 238000001465 metallisation Methods 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 239000002952 polymeric resin Substances 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 229920002379 silicone rubber Polymers 0.000 description 1
- 239000004945 silicone rubber Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 230000002087 whitening effect Effects 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
Landscapes
- Physical Vapour Deposition (AREA)
Abstract
Description
【発明の詳細な説明】 (産業上の利用分野) 本発明は、金属蒸着転写フィルムに関するものである。[Detailed description of the invention] (Industrial application field) The present invention relates to metallized transfer films.
更に詳しくは、光沢、スクラッチ性、折シ曲げ性、印刷
適性等に優れた金属蒸着転写フィルムに関するものであ
シ、ステッカ−、インモールド及び一般のラベル等の分
野に使用できるものである。More specifically, the present invention relates to a metallized transfer film that has excellent gloss, scratch resistance, bendability, printability, etc., and can be used in fields such as paper, stickers, in-molds, and general labels.
(従来技術)
従来上述のような用途に使用される金属蒸着フィルムは
、基材フィルムK14J離ニスを塗布し、その上に印刷
するか或いはそのまま金属蒸着アンカーコート剤を塗布
し、更にその上に金属蒸着を施し、最後の工程で感熱接
着剤を塗布する方法が取られている。その感熱接着剤は
有機溶剤溶液型接着剤(アクリル系樹脂、アルキル−フ
ェノール系樹脂等)、水系接着剤(エチレン−酢酸ビニ
ール系樹脂、塩酢ビ系樹脂等)であシ、ロールコータ−
、グラビアコーター及びナイフコーター等で塗布されて
いる。また、上記金属蒸着転写フィルムを作製時或いは
、被転写体と貼合後印刷する事も可能である。(Prior art) Metal vapor deposited films conventionally used for the above-mentioned purposes are coated with a base film K14J release varnish, printed on it, or directly coated with a metal vapor deposition anchor coating agent, and then coated with a metal vapor deposition anchor coating agent. The method used is to perform metal vapor deposition and apply heat-sensitive adhesive in the final step. The heat-sensitive adhesives are organic solvent solution adhesives (acrylic resins, alkyl-phenol resins, etc.), water-based adhesives (ethylene-vinyl acetate resins, salt-vinyl acetate resins, etc.), and roll coater adhesives.
, gravure coater, knife coater, etc. Further, it is also possible to print the metal vapor-deposited transfer film at the time of production or after bonding it to the object to be transferred.
(発明が解決しようとする問題点)
上記従来技術は、感熱接着剤層が一般的に非常に薄いた
め(1〜5μ)′、被転写体に貼合した場合、スクラッ
チ性、折シ曲げ性、光沢、印刷適性(特に、オフセット
印刷)等が劣る。また、水系接着剤の場合は金属蒸着の
腐蝕も問題となる。(Problems to be Solved by the Invention) In the above-mentioned conventional technology, since the heat-sensitive adhesive layer is generally very thin (1 to 5 μm), it has poor scratch resistance and bending resistance when bonded to a transfer object. , gloss, printability (especially offset printing), etc. are poor. Furthermore, in the case of water-based adhesives, corrosion of metal vapor deposition also becomes a problem.
(問題点を解決するための手段)
本発明者らは上記問題点を解決するため鋭意検討した結
果、上述蒸着転写フィルムに於いて、接着剤層を固型分
100ヂの樹脂で、その樹脂の塗膜が8μ以上の厚みを
有し、加工温度が250℃以下でラミネーシロン可能な
樹脂を使用する事によシ、上記問題点を解決できること
を見出し、本発明に致った。(Means for Solving the Problems) As a result of intensive studies by the present inventors to solve the above-mentioned problems, in the above-mentioned vapor-deposited transfer film, the adhesive layer is made of a resin with a solid content of 100°, and the resin The inventors have discovered that the above problems can be solved by using a resin that has a coating thickness of 8 microns or more and can be laminated at a processing temperature of 250° C. or lower, resulting in the present invention.
以下本発明を図面を用いて更に詳しく説明する。The present invention will be explained in more detail below using the drawings.
第1図のように耐熱性、寸法安定性に優れた基材フィル
ム(1)の片面に該基材フィルム(1)と剥離容易で、
且つ金属蒸着層との密着性に優れた樹脂層(2)を塗布
し、その上に金属蒸着M(3)を施し金属蒸着積層体を
作製する。次に、金属蒸着層(3)と被転写体との双方
に接着性を有する固型分100チの樹脂で、上記積層体
の金属蒸着層(3)に8μ以上の樹脂厚み〔樹脂層(4
)〕で、かつ225℃以下の加工温度でコーティングし
た金属蒸着転写フィルムである。As shown in Fig. 1, one side of the base film (1) has excellent heat resistance and dimensional stability, and the base film (1) is easily peeled.
A resin layer (2) having excellent adhesion to the metal vapor deposited layer is applied, and metal vapor deposition M (3) is applied thereon to produce a metal vapor deposited laminate. Next, a resin having a solid content of 100 cm that has adhesive properties to both the metal vapor deposited layer (3) and the transferred object is applied to the metal vapor deposited layer (3) of the laminate to a resin thickness of 8 μ or more [resin layer ( 4
)] and is a metallized transfer film coated at a processing temperature of 225°C or less.
また、第2図のように基材フィルム(1)に剥離ニス(
6)を塗布し、その上に金属蒸着アンカー剤(7)を施
しても良い。In addition, as shown in Figure 2, the base film (1) is coated with a release varnish (
6) may be applied, and then a metal vapor deposition anchor agent (7) may be applied thereon.
基材フィルム(1)としては、キャリアフィルムとして
使用するため耐熱性、寸法安定性に優れた未処理二軸延
伸プリプロピレンフィルム、未処理ポリエステルフィル
ム等が優れておシ、その他複合フィルム、共押出フィル
ム、紙等も使用する事ができる。As the base film (1), untreated biaxially oriented polypropylene film, untreated polyester film, etc., which have excellent heat resistance and dimensional stability, are suitable for use as a carrier film, as well as other composite films and coextruded films. Film, paper, etc. can also be used.
次に、樹脂層(2)としては金属蒸着転写フィルムを作
製する時は剥がれず、また被転写体に貼合後は基材フィ
ルム(1)が容易に剥がれる必要がある。なお、その樹
脂層(2)は透明でも着色していても良い。そのため樹
脂としてはニトロセルロース樹脂、アクリル樹脂、?リ
ワレタン樹脂、セルロースアセテートグロビオネート樹
脂、セルロースアセテートブチレート樹脂等が使用でき
、これらを二種類以上混合して、剥離性と接着性を改善
する事も可能である。また、基材フィルム(1)の上に
アクリル系樹脂等の剥離ニスを塗布し、その上に前記樹
脂を蒸着アンカー剤として施しても良い。Next, the resin layer (2) must not be peeled off when producing the metallized transfer film, and the base film (1) must be easily peeled off after being bonded to the object to be transferred. Note that the resin layer (2) may be transparent or colored. Therefore, the resins are nitrocellulose resin, acrylic resin, etc. Riwarethane resin, cellulose acetate globionate resin, cellulose acetate butyrate resin, etc. can be used, and it is also possible to improve the releasability and adhesion by mixing two or more of these. Alternatively, a release varnish such as an acrylic resin may be applied onto the base film (1), and the resin may be applied thereon as a vapor deposition anchor agent.
次に、金属蒸着層(3)は通常の真空蒸着機によシ全面
に蒸着して形成する。金属としては、アルミニウム、錫
、鎖、ニッケル等を使用し、真空度10”” 〜10−
’ Pa 、 100〜1000Xの膜厚で蒸着を行
ない金属光沢を有する膜を作る。Next, a metal vapor deposition layer (3) is formed by vapor deposition on the entire surface using a normal vacuum vapor deposition machine. Aluminum, tin, chain, nickel, etc. are used as the metal, and the degree of vacuum is 10" to 10-
'Pa, vapor deposition is performed to a film thickness of 100 to 1000X to produce a film with metallic luster.
次に、上記核層(1〜3)よりなる金属蒸着積層体の金
属蒸着層(3)に塗工する樹脂層(4)を形成する固型
分100チの樹脂としてはエチレン−アクリル酸共重合
体樹脂、エチレン−酢酸ビニル共重合体樹脂及びその酸
変性物、エチレン−アクリル酸エステル共重合体樹脂及
びその酸変性物等の1種又は2種以上を組み合わせても
良い。Next, as a resin having a solid content of 100 g to form a resin layer (4) to be coated on the metal vapor deposited layer (3) of the metal vapor deposited laminate consisting of the core layers (1 to 3), ethylene-acrylic acid is used. One type or a combination of two or more of polymer resins, ethylene-vinyl acetate copolymer resins and acid-modified products thereof, ethylene-acrylic acid ester copolymer resins and acid-modified products thereof, etc. may be used.
また、粘着付与剤(ロジン、ロジン変性樹脂、チル(ン
樹脂、チル(ン変性樹脂、脂肪族炭化水素樹脂、芳香族
炭化水素樹脂、ケトン樹脂、環化デム等)、ワックス(
)母ラフインワックス、低分子ポリエチレン、合成ワッ
クス等)、ポリエチレン及びその変性物等を適宜加える
事ができる。また助剤として酸化防止剤、スリラグ剤、
ゾロッキング防止剤等を加える事も差しつかえない。In addition, tackifiers (rosin, rosin modified resin, chill resin, chill modified resin, aliphatic hydrocarbon resin, aromatic hydrocarbon resin, ketone resin, cyclized dem, etc.), wax (
) mother rough-in wax, low-molecular polyethylene, synthetic wax, etc.), polyethylene and modified products thereof, etc. can be added as appropriate. In addition, antioxidants, slylag agents,
There is no harm in adding anti-zolocking agents, etc.
上記樹脂層(4)は8μ未満の厚みでは、紙、布等のポ
ー2スな被転写体と加熱、加圧して転写した場合下地を
充分かくす事ができないため、超光沢が得られない。ま
九、スクラッチ性、折多曲げ適性、印刷適性が劣る。最
適膜厚は10〜50μである。また加工温度250℃以
上になると金属蒸着層(3)の上に塗布した樹脂層(2
)、−1!たけ剥離ニス(6)、蒸着アンカー剤(7)
の耐熱性がないため金属蒸着に白シやクラックが発生し
、充分な光沢が得られない。If the thickness of the resin layer (4) is less than 8 μm, when it is transferred to a porous object such as paper or cloth by heating and pressurizing, it will not be able to sufficiently hide the base, so that super gloss will not be obtained. Poor scratch resistance, bendability, and printability. The optimum film thickness is 10-50μ. In addition, when the processing temperature exceeds 250°C, the resin layer (2) coated on the metal vapor deposited layer (3)
), -1! Bamboo release varnish (6), vapor deposition anchor agent (7)
Because of the lack of heat resistance, white spots and cracks occur in metal vapor deposition, making it impossible to obtain sufficient gloss.
次忙、本発明の金属蒸着フィルムの被転写体としては、
紙、布、木材等のポーラスな基材、或いはフィルム、シ
ート、成型品等のノンポーラスな基材でも良く、またこ
れらを組み合わせても良い。The object to be transferred with the metallized film of the present invention is as follows:
It may be a porous base material such as paper, cloth, or wood, or a non-porous base material such as a film, sheet, or molded product, or a combination of these may be used.
以上のような構成からなる本発明の金属蒸着転写フィル
ムを被転写体に転写するにゆ当該金属蒸着転写フィルム
を被転写体に重ねて、加熱、加圧し、冷却後被転写体か
ら基材フィルム(1)を剥がす方法、或いはプラスチッ
ク成型容器の金型内に当該金属蒸着転写フィルムを供給
し、容器と一体成型後基材フィルムを剥がす方法等があ
る。In order to transfer the metallized transfer film of the present invention having the above-described structure onto a transfer object, the metallization transfer film is placed on the transfer object, heated and pressurized, and after cooling, the base film is removed from the transfer object. There is a method in which (1) is peeled off, or a method in which the metal vapor-deposited transfer film is supplied into a mold of a plastic molded container and the base film is peeled off after integrally molding with the container.
(実施例)
〈実施例1〉
厚さ20μの未処理二軸延伸ポリプロピレンフィルム(
東京セロファン紙(株)製)の片側に下記の組成の剥離
ニス:
ニトロセルロース系樹脂 14部ポリウレタン
樹脂 6N酢酸エチル
80#を、版深度30μのグラビア版で全面均
一に塗布した。次に下記組成のアルミ蒸着用アンカー剤
ニアクリル系樹脂 20部メチルエチ
ルケトン 4ON酢酸エチル
40〃を、版深度30μのグラビア版で剥1
1 ニスの上に塗布した。次に、上記アルミ蒸着用アン
カーコート剤の上に、真空蒸着機を使用し、10””
Paの真空度で400又のアルミ蒸着層を形成した。次
に、上記積層体のアルミ蒸着層に下記の固型分100チ
樹脂:
エチレンー酢酸ビニル共重合体 40部低分子量?
リエチレンワックス 10〃で、押出コーティ
ング法を使用し、加工温度220℃、樹脂膜厚30μで
コーティングを行ない金属蒸着転写フィルムを作製した
。(Example) <Example 1> Untreated biaxially oriented polypropylene film with a thickness of 20μ (
Release varnish with the following composition on one side of Tokyo Cellophane Paper Co., Ltd.: Nitrocellulose resin 14 parts Polyurethane resin 6N ethyl acetate
80# was applied uniformly over the entire surface using a gravure plate with a plate depth of 30 μm. Next, Niacrylic resin as an anchor for aluminum deposition with the following composition: 20 parts methyl ethyl ketone 4ON ethyl acetate
40〃 with a gravure plate with a plate depth of 30μ1
1 Applied over varnish. Next, a vacuum evaporator was used to coat the anchor coating agent for aluminum evaporation, and 10"
A 400-layer aluminum vapor deposition layer was formed at a vacuum degree of Pa. Next, the following solid content: 100 parts resin: Ethylene-vinyl acetate copolymer 40 parts Low molecular weight?
A metallized transfer film was prepared by coating with 10% polyethylene wax using an extrusion coating method at a processing temperature of 220° C. and a resin film thickness of 30 μm.
次に上記金属蒸着転写フィルギを85ノ/m2のサラン
クラフト紙に密着させ、表面温度150℃ノシリコンラ
パーロールニテ、圧力2に9/cIrL!、スピード5
Vmlnの条件で転写を行ない、その後、基材フィル
ムを剥離して剥離ニス上面にオフセット印刷を行なった
。Next, the metal vapor-deposited transfer film was placed in close contact with Saran Kraft paper at 85 cm/m2, with a surface temperature of 150°C, a silicon wrapper roll, and a pressure of 2 to 9/cIrL! , speed 5
Transfer was performed under conditions of Vmln, and then the base film was peeled off and offset printing was performed on the top surface of the release varnish.
その結果は表−1で示す通シ、全て良好であった。The results shown in Table 1 were all good.
〈実施例2〉
実施例1の剥離ニスとアルミ蒸着用アンカーコート剤の
代シに、下記の剥離機能及びアルば蒸着アンカー機能を
兼ね備えた樹脂:
ポリウレタン樹脂 10部酢酸エチル
4ONメチルエチルケトン
4ONを、版深度30μのグラビア版で全面
均一に塗布した以外は同様に行なった。<Example 2> In place of the release varnish and anchor coating agent for aluminum deposition in Example 1, a resin having the following release function and aluminum deposition anchor function was used: Polyurethane resin 10 parts Ethyl acetate 4ON methyl ethyl ketone
The same procedure was carried out except that 4ON was applied uniformly over the entire surface using a gravure plate with a plate depth of 30 μm.
その結果は表−1で示す通シ、全て良好であった。The results shown in Table 1 were all good.
〈実施例3〉
実施例2の未処理二軸延伸、91Jプロピレンフイルム
の代シに25μの未処理ポリエステルフィルムを使用し
、被転写体のサランクラフト紙の代シに200μの一す
プロピレンシートを使用し、表面温度200℃のシリコ
ンラバーロールで行なう以外は同様に行なった。<Example 3> A 25μ untreated polyester film was used as a substitute for the untreated biaxially stretched 91J propylene film of Example 2, and a 200μ monopropylene sheet was used as a substitute for Saran Kraft paper as the transfer target. The same procedure was carried out except that a silicone rubber roll having a surface temperature of 200° C. was used.
その結果は表−1で示す通シ全て良好であった。The results shown in Table 1 were all good.
〈実施例4〉
実施例3の金属蒸着転写フィルムをポリプロピレン成型
容器の金型内に供給し、ポリプロピレン樹脂を220℃
で注入、圧カフ 00 kl/CrrL”、インジェク
シ冒ンタイム5秒、トータルサイクルタイム40秒の条
件で金属蒸着転写フィルムと一体成型した。その後基材
フィルムを剥離した。<Example 4> The metallized transfer film of Example 3 was supplied into the mold of a polypropylene molding container, and the polypropylene resin was heated at 220°C.
The sample was injected with a pressure cuff of 00 kl/CrrL'', the injection time was 5 seconds, and the total cycle time was 40 seconds.The base film was then peeled off.
その結果は表−1で示す通シ全て良好でありた。The results shown in Table 1 were all good.
〈比較例1〉
実施例2の固型分100%の樹脂の代シに、アルキル−
フェノール樹脂を塗肌4μにする以外は同様に行なった
。<Comparative Example 1> In place of the resin with a solid content of 100% in Example 2, alkyl-
The same procedure was carried out except that the phenol resin was applied to the skin to a thickness of 4 μm.
その結果は表−1に示す通シ光沢、スクラッチ性、折シ
曲げ性、印刷適性が劣シ、特に印刷(オフセット)適性
が一番劣っていた。The results are shown in Table 1, with poor through-gloss, scratch resistance, bendability, and printability, with printing (offset) suitability being the worst.
〈比較例2〉
実施例2の固型分100%の樹脂の代シK、エチレン−
酢酸ビニール共重合体エマルジ嘗ンを塗膜4μにする以
外は同様に行なった。<Comparative Example 2> Instead of the resin with a solid content of 100% in Example 2, K, ethylene-
The same procedure was carried out except that the coating film thickness of the vinyl acetate copolymer emulsion was 4 μm.
その結果は表−1に示す通シ、光沢、スクラッチ性、折
シ曲げ性、腐蝕、印刷適性、耐水性が劣シ、特ニスクラ
ッチ性、腐蝕、印刷(オフセット)適性が劣っていた。The results are shown in Table 1: poor throughput, gloss, scratch resistance, bendability, corrosion, printability, and water resistance, and poor scratch resistance, corrosion, and printing (offset) suitability.
〈比較例3〉
実施例3の固型分100%の樹脂の代シにアクリルエマ
ルジ冒ンを塗膜4μにする以外は同様に行なった。<Comparative Example 3> The same procedure was carried out as in Example 3, except that instead of the resin having a solid content of 100%, an acrylic emulsion was used to form a coating film of 4 μm.
その結果は表−1に示す通シ、スクラッチ性、折シ曲げ
性、腐蝕、印刷(オフセット)適性が劣っていた。The results shown in Table 1 were poor in perforation, scratch resistance, bendability, corrosion, and printing (offset) suitability.
(評価試験方法)
1)光沢
日本電色(株)製反射光沢計(VG−ID型)を用いて
入射角60度、反射角60度にて反射光沢を測定した(
JISK−540Or塗料一般試験方法」6−7項に
依る)。(Evaluation test method) 1) Gloss Reflection gloss was measured at an incident angle of 60 degrees and a reflection angle of 60 degrees using a reflection gloss meter (VG-ID type) manufactured by Nippon Denshoku Co., Ltd. (
(according to section 6-7 of "JISK-540 Or Paint General Test Methods").
2)クラック 目視による。2) crack By visual inspection.
3)クモリ 目視による。3) Spider By visual inspection.
4)スクラッチ
JISK−540Or塗料一般試験方法J6−14項に
基づき、三菱UNI鉛筆Hを用いて試験した。4) Scratch JISK-540Or Paint General Test Methods Tested using Mitsubishi UNI Pencil H based on J6-14.
但し荷重は10.P−1=0.005Pとした。However, the load is 10. P-1=0.005P.
5)折シ曲げ
15αX15cr!Lの試料を蒸着面を上にして相対す
る角部を合せて折シ曲げ、折目が180度になるよう指
で強く押した後元に戻して、該折シ目にセロファンテー
プを貼り合せ、ゆっくシと90度方向に引き剥がした(
谷折シ)。又15crILX15cIILの試料を蒸着
面を下にして同様な試験をした(山折シ)。そして、セ
ロファンテープによシ剥がれた蒸着面を目視によシ判定
した。5) Bending 15αX15cr! Fold the sample L with the vapor-deposited side facing up, aligning the opposing corners, press firmly with your fingers so that the fold is 180 degrees, then put it back together and attach cellophane tape to the fold. , and slowly peeled it off in a 90 degree direction (
Taniorishi). A similar test was also conducted using a sample of 15crILX15cIIL with the vapor deposition side facing down (mountain folding). Then, the vapor-deposited surface that was peeled off by the cellophane tape was visually judged.
6)腐蝕
試料の蒸着面を上にして温度40℃±1℃、湿度80チ
±1チに保持した恒温恒湿槽に入れ、96時間後に取シ
出し、温度40℃で30分間乾燥し、蒸着金属の腐蝕に
よる欠落を目視によシ判定した。6) Place the corrosion sample with the vapor deposition side facing up in a constant temperature and humidity chamber maintained at a temperature of 40°C ± 1°C and a humidity of 80°C ± 1°C, take it out after 96 hours, and dry it for 30 minutes at a temperature of 40°C. Missing parts due to corrosion of the deposited metal were visually determined.
7)印刷適性
(失明製作所製R1テスター2型オフセット印刷機を用
いて、ニエーダイキュア2〔大日本インキ化学工業(鉛
製紫外線硬化型インキ〕によ〕印刷し、アイガラフィッ
クス@) jJJ UB−06型紫外線照射装置にて、
80 Wkn、20m/minの条件で硬化乾燥させ、
インキの転移性、密着性、紙ムケ性を判定した。7) Printability (Printed with Niedai Cure 2 [Dainippon Ink and Chemicals (lead-based ultraviolet curable ink)] using a R1 Tester 2 type offset printing machine made by Shimeme Seisakusho, and Aigara Fix @) jJJ UB -06 type ultraviolet irradiation equipment,
Cured and dried under the conditions of 80 Wkn and 20 m/min,
Ink transferability, adhesion, and paper smearing properties were evaluated.
8)耐水性
25℃に保った蒸留水中に2時間浸漬した後室温にて2
時間乾燥し、蒸着面にフクレ、ハガレ、白化、クラック
の有無を目視によシ判定した。8) Water resistance After immersing in distilled water kept at 25℃ for 2 hours,
After drying for a period of time, the presence or absence of blisters, peeling, whitening, and cracks on the deposited surface was visually determined.
(発明の効果)
本発明の金属蒸着転写フィルムは従来の金属蒸着紙に比
べ、スクラッチ性、折シ曲げ性、印刷適性等が優れてお
り、更に被転写材としての選択が自由、紙の調湿が不要
等の特徴が得られる。(Effects of the Invention) The metallized transfer film of the present invention has superior scratch resistance, bendability, printability, etc. compared to conventional metallized paper, and is also flexible in its selection as a material to be transferred. Features such as no need for moisture can be obtained.
第1図及び第2図は本発明の実施例を示す金属蒸着転写
フィルムの断面図を示す。
1・・・基材フィルム、2・・・剥離、蒸着アンカー兼
用樹脂層、3・・・金属蒸着層、4・・・固型分100
%樹脂による樹脂層。
代理人 弁理士 高 橋 勝 利
第1図
第2図1 and 2 show cross-sectional views of metallized transfer films showing embodiments of the present invention. DESCRIPTION OF SYMBOLS 1... Base film, 2... Peeling and vapor deposition anchor double duty resin layer, 3... Metal vapor deposition layer, 4... Solid content 100
Resin layer by % resin. Agent Patent Attorney Katsutoshi Takahashi Figure 1 Figure 2
Claims (1)
且つ金属蒸着適性を有する樹脂層(2)、金属蒸着層(
3)、樹脂層(4)が順次積層されてた金属蒸着転写フ
ィルムであって、上記樹脂層(4)が8μ以上の層厚を
有し、該樹脂層は固型分100%の樹脂によって成形さ
れ、かつ該固型分100%の樹脂の溶融温度が250℃
以下であることを特徴とする上記金属蒸着転写フィルム
。 2、樹脂層(2)が剥離ニスと金属蒸着アンカーコート
剤から成ることを特徴とする特許請求の範囲第1項に記
載の金属蒸着転写フィルム。 3、基材フィルムの片面に該フィルムと剥離容易で金属
蒸着適性を有する樹脂を塗布し、次いで該樹脂層上に金
属蒸着を行ない金属蒸着積層体を作製し、しかる後上記
金属蒸着積層体の金属蒸着層側に溶融温度250℃以下
の固型分100%樹脂を8μ以上の厚みに塗布すること
を特徴とする金属蒸着転写フィルムの製造方法。[Claims] 1. A base film (1), a resin layer (2) that is easily peelable from the base film and has metal vapor deposition suitability, a metal vapor deposited layer (
3) A metallized transfer film in which resin layers (4) are sequentially laminated, the resin layer (4) has a layer thickness of 8μ or more, and the resin layer is made of a resin with a solid content of 100%. The melting temperature of the resin that is molded and has a solid content of 100% is 250°C.
The above metallized transfer film, characterized in that: 2. The metallized transfer film according to claim 1, wherein the resin layer (2) comprises a release varnish and a metallized anchor coating agent. 3. Coat one side of the base film with a resin that is easily peelable from the film and suitable for metal vapor deposition, then perform metal vapor deposition on the resin layer to produce a metal vapor deposited laminate, and then apply the metal vapor deposited laminate to the base film. A method for producing a metal vapor-deposited transfer film, which comprises applying a 100% solid resin having a melting temperature of 250° C. or less to a thickness of 8 μm or more on the metal vapor-deposited layer side.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP62197062A JP2623590B2 (en) | 1987-08-06 | 1987-08-06 | Metallized transfer film and method for producing the same |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP62197062A JP2623590B2 (en) | 1987-08-06 | 1987-08-06 | Metallized transfer film and method for producing the same |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH01147054A true JPH01147054A (en) | 1989-06-08 |
JP2623590B2 JP2623590B2 (en) | 1997-06-25 |
Family
ID=16368080
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP62197062A Expired - Fee Related JP2623590B2 (en) | 1987-08-06 | 1987-08-06 | Metallized transfer film and method for producing the same |
Country Status (1)
Country | Link |
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JP (1) | JP2623590B2 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2006321088A (en) * | 2005-05-18 | 2006-11-30 | Oike Ind Co Ltd | High barrier film |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS61273568A (en) * | 1985-05-29 | 1986-12-03 | Toppan Printing Co Ltd | Hologram transfer foil |
-
1987
- 1987-08-06 JP JP62197062A patent/JP2623590B2/en not_active Expired - Fee Related
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS61273568A (en) * | 1985-05-29 | 1986-12-03 | Toppan Printing Co Ltd | Hologram transfer foil |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2006321088A (en) * | 2005-05-18 | 2006-11-30 | Oike Ind Co Ltd | High barrier film |
Also Published As
Publication number | Publication date |
---|---|
JP2623590B2 (en) | 1997-06-25 |
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