JP3295858B2 - Transfer film with improved transfer layer - Google Patents

Transfer film with improved transfer layer

Info

Publication number
JP3295858B2
JP3295858B2 JP35290192A JP35290192A JP3295858B2 JP 3295858 B2 JP3295858 B2 JP 3295858B2 JP 35290192 A JP35290192 A JP 35290192A JP 35290192 A JP35290192 A JP 35290192A JP 3295858 B2 JP3295858 B2 JP 3295858B2
Authority
JP
Japan
Prior art keywords
resin
film
transfer
layer
matte
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
Application number
JP35290192A
Other languages
Japanese (ja)
Other versions
JPH06179283A (en
Inventor
智子 岩佐
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Dai Nippon Printing Co Ltd
Original Assignee
Dai Nippon Printing Co Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Dai Nippon Printing Co Ltd filed Critical Dai Nippon Printing Co Ltd
Priority to JP35290192A priority Critical patent/JP3295858B2/en
Publication of JPH06179283A publication Critical patent/JPH06179283A/en
Application granted granted Critical
Publication of JP3295858B2 publication Critical patent/JP3295858B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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  • Printing Methods (AREA)
  • Decoration By Transfer Pictures (AREA)
  • Laminated Bodies (AREA)
  • Paints Or Removers (AREA)

Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【産業上の利用分野】本発明は、転写時に膜切れ性が良
く、転写作業が能率良くできる艶消し転写フイルムに関
するものである。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a matte transfer film which has a good film-cutting property at the time of transfer and enables efficient transfer operation.

【0002】[0002]

【従来の技術】従来、転写方式による艶消しのスウェー
ド調を出す方法として、粗粒(粒度分布の最頻出粒径が
10〜40μm程度)の樹脂ビーズ顔料を添加した樹脂
を使用して、基材フイルムにコーティングして艶消し転
写フイルムを作製していたが、バインダー単体の時より
塗膜は脆くなり、耐擦傷性が低下した。艶消し樹脂の耐
擦傷性を向上させるために、弾力性があり、造膜力の強
い樹脂(ウレタンエラストマー等のポリウレタン樹脂
等)を使用したが、塗膜の強度が強くなり、転写時に基
材フイルムを剥離したとき、転写層が被転写体の周縁の
ところで完全に切断されずに、図1(a)に示すような
バリが生じ、このバリを除去する後工程が必要になっ
た。
2. Description of the Related Art Conventionally, as a method for producing a matte suede tone by a transfer method, a resin to which a resin bead pigment of coarse particles (the most frequent particle size of particle size distribution is about 10 to 40 μm) is used is used. A matte transfer film was produced by coating the material film, but the coating film became brittle and the abrasion resistance was reduced as compared with the case of using only the binder. In order to improve the scratch resistance of the matting resin, a resin with elasticity and strong film forming power (polyurethane resin such as urethane elastomer) was used. When the film was peeled off, the transfer layer was not completely cut at the peripheral edge of the object to be transferred, and burrs were formed as shown in FIG. 1A, and a post-process for removing the burrs became necessary.

【0003】[0003]

【発明が解決しようとする課題】賦型性フイルム(基材
フイルム表面に艶消し用の微細な凹凸模様を設けたフイ
ルム)に樹脂ビーズ顔料を含む艶消し樹脂層を形成した
転写フイルムにおいて、艶消し樹脂層の耐擦傷性を向上
させるために造膜力の強い樹脂を使用しているため、塗
膜の強度が強くなり、転写時に賦型フイルムを剥離した
とき、転写層が被転写体の周縁のところで完全に切断さ
れずに、図1(a)に示すようなバリが生じる。そのた
め、そのバリの除去工程が必要となり、作業効率が低下
する。以上の背景から、艶消し樹脂層の耐擦傷性が良
く、しかも被転写体へ転写した時、膜切れ性の良い転写
フイルムが要望されるようになった。本発明はこの要望
に応え、膜切れ性を改良した転写フイルムを提供するこ
とを目的とする。
SUMMARY OF THE INVENTION In a transfer film in which a matting resin layer containing a resin bead pigment is formed on a formable film (a film having a fine uneven pattern for matting on the surface of a base film), Since the resin with strong film forming power is used to improve the abrasion resistance of the eraser resin layer, the strength of the coating film becomes strong, and when the shaping film is peeled off at the time of transfer, the transfer layer becomes Burrs as shown in FIG. 1A occur without being completely cut at the periphery. Therefore, a step of removing the burrs is required, and the working efficiency is reduced. From the above background, there has been a demand for a transfer film having good scratch resistance of the matte resin layer and good cut-off property of the film when transferred to an object to be transferred. An object of the present invention is to provide a transfer film which meets this demand and has improved film-cutting properties.

【0004】[0004]

【課題を解決するための手段】基材フイルムの表面に転
写層として少なくとも、樹脂ビーズ顔料を含む艶消し樹
脂層及び接着剤層を積層してなる転写フイルムであっ
て、艶消し樹脂に粒径0.1μm以下のシリカ又は沈降
性硫酸バリウムを0.25〜0.5重量%添加して、転
写層の膜切れ性を改良する方法とした。また、基材フイ
ルムの表面に転写層として少なくとも、樹脂ビーズ顔料
を含む艶消し樹脂層、絵柄層及び接着剤層を積層してな
る転写フイルムであって、接着剤層に粒径0.1μm以
下のシリカ又は沈降性硫酸バリウムを1〜2重量%添加
して、転写層の膜切れ性を改良する方法とした。艶消し
樹脂又は接着剤層に添加するシリカ又は沈降性硫酸バリ
ウムは、上記添加量以上では表面光沢度(艶消し程度)
が変わったり、耐擦傷性が劣化する。上記添加量以下で
は、膜切れの改良効果がでない。
A transfer film comprising at least a matting resin layer containing a resin bead pigment and an adhesive layer as a transfer layer on the surface of a substrate film, wherein the matting resin has a particle size. Silica or sedimentable barium sulfate of 0.1 μm or less was added in an amount of 0.25 to 0.5% by weight to improve the cut-off property of the transfer layer. Further, at least as a transfer layer on the surface of the base film, a matte resin layer containing a resin bead pigment, a pattern layer and an adhesive layer laminated on the transfer film, the adhesive layer having a particle size of 0.1 μm or less Of silica or precipitated barium sulfate was added in an amount of 1 to 2% by weight to improve the film breakability of the transfer layer. When the amount of silica or precipitated barium sulfate added to the matting resin or the adhesive layer is more than the above amount, the surface glossiness (degree of matting)
Or the scratch resistance deteriorates. If the amount is less than the above-mentioned amount, the effect of improving film breakage is not obtained.

【0005】以下に上記転写フイルムを製造する場合の
基材フイルム、バインダー樹脂、ビーズ顔料、接着剤、
微粒子等について記す。基材フイルムは艶消し樹脂層と
剥離性を有するフイルムであればよく、基材フイルムの
材質は、例えば、ポリエチレンテレフタレート、ポリブ
チレンテレフタレート等のポリエステル、ポリエチレ
ン、ポリプロピレン等のポリオレフィン、アクリル、ポ
リカーボネート、ポリアリレート、ポリアミド、ポリ塩
化ビニル、ポリスチレン、ポリフッ化ビニル、ポリテト
ラクロロエチレン、テフロン、ポリフッ化ビニリデン、
ポリビニルアルコール、ポリエーテルエーテルケトン、
ポリイミド、セロハン等からなるフイルムを単体で、或
いはそれらのフイルム同志を貼り合わせたり、その樹脂
を直接塗布して積層フイルムとしたもの、又はアルミ箔
と複合させたもの等が挙げられ、中でも二軸延伸ポリエ
チレンテレフタレートフイルム(以下PETフイルムと
する)が最も好ましい。
A base film, a binder resin, a bead pigment, an adhesive,
The fine particles and the like will be described. The base film may be a film having a matte resin layer and a peeling property, and the material of the base film is, for example, polyethylene terephthalate, polyester such as polybutylene terephthalate, polyethylene, polyolefin such as polypropylene, acrylic, polycarbonate, or poly. Arylate, polyamide, polyvinyl chloride, polystyrene, polyvinyl fluoride, polytetrachloroethylene, teflon, polyvinylidene fluoride,
Polyvinyl alcohol, polyether ether ketone,
Polyimide, cellophane film or the like alone, or those films are bonded together, or the resin is directly applied to form a laminated film, or composite with aluminum foil. Stretched polyethylene terephthalate film (hereinafter referred to as PET film) is most preferred.

【0006】基材フイルムは艶消し樹脂層との離型性を
高める目的で、必要に応じ、アクリル、メラミン、ウレ
タン、エポキシ等の樹脂、ポリエステルアクリレート、
ウレタンアクリレート、2- ヒドロキシエチルアクリレ
ート、ネオペンチルグリコールジアクリレート等からな
る熱硬化性又は電離放射線硬化性樹脂等の離型性樹脂に
ワックス、シリコーン等の離型性の物質を添加した離型
剤を用いて、公知の離型処理を施すことができる。
For the purpose of enhancing the releasability of the matte resin layer from the matte resin layer, a resin such as acrylic, melamine, urethane, epoxy, polyester acrylate,
A release agent obtained by adding a release material such as a wax or silicone to a release resin such as a thermosetting or ionizing radiation-curable resin composed of urethane acrylate, 2-hydroxyethyl acrylate, neopentyl glycol diacrylate, or the like. A known release treatment can be performed by using this.

【0007】本発明において、艶消し樹脂層の艶消し効
果を更に高めるために、図2に示すように、基材フイル
ムの表面に艶消し用の微細凹凸模様を設けたフイルム
(即ち、賦型フイルム)を用いてもよい。微細凹凸模様
は上記の基材フイルムの表面にサンドブラスト加工やケ
ミカルエッチングを施す方法、基材フイルム中に艶消し
剤を練り込む方法、又、離型剤の中に艶消し剤を添加し
た微細凹凸塗膜層を形成する方法で設けることもでき
る。尚、基材フイルムは表面に凹凸模様を形成せずに平
滑にしてもよい。
In the present invention, in order to further enhance the matting effect of the matting resin layer, as shown in FIG. 2, a film having a fine uneven pattern for matting on the surface of a base film (that is, a mold). Film). The method of sandblasting or chemical etching on the surface of the above base film, the method of kneading a matting agent in the base film, or the fine unevenness with the addition of a matting agent in the release agent It can also be provided by a method of forming a coating layer. The base film may be smooth without forming an uneven pattern on the surface.

【0008】バインダー樹脂は、熱硬化性樹脂、熱可塑
性樹脂、電離放射線硬化性樹脂等が用いられる。このよ
うな樹脂として例えば、アクリル、キレート硬化型アク
リル、ポリエステルウレタン等やエポキシ硬化型アクリ
ル、アクリルウレタン、ウレタンエラストマー等の樹
脂、ポリエステル、アクリレート、ウレタンアクリレー
ト、2- ヒドロキシエチルアクリレート、ネオペンチル
グリコールジアクリレート等が挙げられる。また、バイ
ンダー樹脂としては上記の樹脂以外に、アクリル樹脂、
塩化ビニル・酢酸ビニル共重合体、ゴム系樹脂、硝酸セ
ルロース等の単体又はそれらを混合してなる樹脂(接着
剤に使用した樹脂)を添加してもよい。即ち、接着剤層
に使用した樹脂と同じ樹脂をバインダー樹脂に添加する
ことで、艶消し樹脂と接着剤層間の密着性を向上させる
ことができる。
[0008] As the binder resin, a thermosetting resin, a thermoplastic resin, an ionizing radiation curable resin, or the like is used. Examples of such a resin include resins such as acrylic, chelate-curable acrylic, and polyester urethane, epoxy-curable acrylic, acrylic urethane, urethane elastomer, polyester, acrylate, urethane acrylate, 2-hydroxyethyl acrylate, and neopentyl glycol diacrylate. And the like. As the binder resin, in addition to the above resins, acrylic resin,
A single substance such as a vinyl chloride / vinyl acetate copolymer, a rubber-based resin, cellulose nitrate, or a mixture thereof (a resin used for the adhesive) may be added. That is, by adding the same resin as the resin used for the adhesive layer to the binder resin, the adhesion between the matting resin and the adhesive layer can be improved.

【0009】バインダー樹脂としては、艶消し樹脂層の
耐擦傷性、可撓性の点から上記の中でもアクリルウレタ
ン、ウレタンエラストマー等が好ましく、具体的には分
子中に活性水素を有する直鎖状のポリオールと分子中に
イソシアネート基を有する化合物とを反応させて得られ
る熱可塑性ポリウレタン樹脂がある。熱可塑性ポリウレ
タン樹脂の直鎖状のポリオール化合物として、芳香族又
はスピロ環骨格を有するジオール化合物とラクトン化合
物又はその誘導体又はエポキシ化合物との付加反応生成
物、フタル酸等の二塩基酸とエチレングリコール等のポ
リオールとの縮合生成物、及び環状エステル化合物から
誘導される開環ポリエステル化合物等のポリエステルポ
リオール、ポリテトラメチレンエーテルグリコール、ポ
リエチレングリコール、ポリプロピレングリコールなど
のポリエーテルポリオール及びポリカーボネートポリオ
ール、ポリエステルアミドポリオール等が挙げられる。
As the binder resin, acrylic urethane, urethane elastomer and the like are preferable among the above in view of the scratch resistance and flexibility of the matting resin layer. Specifically, a linear resin having active hydrogen in the molecule is preferred. There is a thermoplastic polyurethane resin obtained by reacting a polyol with a compound having an isocyanate group in the molecule. As a linear polyol compound of a thermoplastic polyurethane resin, an addition reaction product of a diol compound having an aromatic or spiro ring skeleton and a lactone compound or a derivative thereof or an epoxy compound, a dibasic acid such as phthalic acid, and ethylene glycol Condensation products with polyols, and polyester polyols such as ring-opening polyester compounds derived from cyclic ester compounds, polytetramethylene ether glycol, polyethylene glycol, polyether polyols such as polypropylene glycol and polycarbonate polyols, polyester amide polyols and the like. No.

【0010】熱可塑性ポリウレタン樹脂のイソシアネー
ト基を有する化合物としては、トルエンジイソシアネー
ト、ジフェニルメタンジイソシアネート、パラフェニレ
ンジイソシアネート、ジメチルジフェニルジイソシアネ
ート、ジアニシジンジイソシアネート、ナフタレンジイ
ソシアネート、ジシクロヘキシルメタンジイソシアネー
ト、ヘキサメチレンジイソシアネート、トリメチルヘキ
サメチレンジイソシアネート、テトラメチルキシリレン
ジイソシアネート、イソホロンジイソシアネート等のジ
イソシアネート類、又はこれらのイソシアネート単量体
をジオール、トリオールなどのポリオールでウレタン変
成した変成イソシアネート等が挙げられる。特に、イソ
シアネート類は直鎖状で主鎖が長いものが、柔軟で耐擦
傷性に優れた艶消し樹脂層を形成することができるため
に、より好ましく、熱可塑性ウレタン樹脂としては、分
子量が20000〜40000で且つTgが−40℃〜
−30℃のものが好ましい。
Examples of the compound having an isocyanate group of the thermoplastic polyurethane resin include toluene diisocyanate, diphenylmethane diisocyanate, paraphenylene diisocyanate, dimethyldiphenyl diisocyanate, dianisidine diisocyanate, naphthalene diisocyanate, dicyclohexylmethane diisocyanate, hexamethylene diisocyanate, trimethylhexamethylene diisocyanate. Examples thereof include diisocyanates such as tetramethylxylylene diisocyanate and isophorone diisocyanate, and modified isocyanates obtained by subjecting these isocyanate monomers to urethane modification with polyols such as diols and triols. In particular, isocyanates having a straight chain and a long main chain are more preferable because they can form a matte resin layer which is flexible and excellent in scratch resistance. The thermoplastic urethane resin has a molecular weight of 20,000. ~ 40,000 and Tg -40 ° C ~
Those at -30 ° C are preferred.

【0011】接着剤は、被転写体の材質に応じて適宜選
定した接着剤を用いればよく、一般にアクリル樹脂、ビ
ニル系樹脂、ゴム系樹脂、熱可塑性ウレタン樹脂等の単
体又は混合してなるものが使用できる。特に、艶消し樹
脂にウレタンエラストマーと塩化ビニル・酢酸ビニル共
重合体の混合物を使用した場合、塩化ビニル・酢酸ビニ
ル共重合体を上記樹脂に10〜25%程度添加した樹脂
を用いると密着性が向上してより好ましい。また、接着
剤層は艶消し樹脂に接着性を有する材質を使用した場合
には特に形成しなくてもよい。
The adhesive may be an adhesive selected as appropriate according to the material of the object to be transferred, and is generally an acrylic resin, a vinyl resin, a rubber resin, a thermoplastic urethane resin, or a mixture thereof. Can be used. In particular, when a mixture of a urethane elastomer and a vinyl chloride / vinyl acetate copolymer is used as the matting resin, the adhesion is improved when a resin obtained by adding the vinyl chloride / vinyl acetate copolymer to the above resin in an amount of about 10 to 25% is used. Improved and more preferred. Further, the adhesive layer need not be formed particularly when a material having adhesiveness to the matting resin is used.

【0012】膜切れ性改良のため添加する微粒子として
は、シリカ、沈降性硫酸バリウムが特に良好であるが、
この他に、炭酸バリウム、酸化亜鉛、アルミナ、カオリ
ナイトなども使用できる。粒径を0.1μm以下、添加
量を艶消し樹脂層に対しては0.25〜0.5重量%、
接着剤層に対しては1〜2重量%添加すると艶(光沢
度)、耐擦傷性に影響を与えることなく転写層を適度に
脆くし、膜切れ性のみを向上させることができる。微粒
子の粒径としては、最頻出粒径0.02μm、最大粒径
0.04μmのものがよい。また、これら微粒子は接着
剤層と艶消し樹脂層との両方に添加することもできる。
As fine particles to be added for improving film breakability, silica and precipitated barium sulfate are particularly good.
In addition, barium carbonate, zinc oxide, alumina, kaolinite and the like can also be used. The particle size is 0.1 μm or less, the addition amount is 0.25 to 0.5% by weight based on the matte resin layer,
Addition of 1 to 2% by weight of the adhesive layer makes the transfer layer appropriately brittle without affecting gloss (glossiness) and abrasion resistance, and can improve only film breakability. As the particle size of the fine particles, those having a most frequent particle size of 0.02 μm and a maximum particle size of 0.04 μm are preferable. Further, these fine particles can be added to both the adhesive layer and the matting resin layer.

【0013】樹脂ビーズ顔料は、顔料の微粉末を合成樹
脂中に分散したものを粒状に成形したもので、艶消し効
果が高く、どの方向から見ても艶消しになり、特にソフ
トな質感のスウェード調表面を形成することができる。
ビーズ顔料の材質として、例えば、Fe23 、TiO
2 、CaCO3 、キナクリドン等の通常の顔料の微粉末
を用い、該微粉末表面をポリウレタン、アクリル、エポ
キシ、ポリエステル、ナイロン、フッ素樹脂、塩化ビニ
ル樹脂等の弾力性のある樹脂、又はこれに、必要に応じ
て可塑剤、安定剤、界面活性剤等を加えたもので覆った
もの、或いは該顔料微粉末を該弾力性樹脂中に分散させ
たものが挙げられる。
[0013] Resin bead pigment is obtained by dispersing a fine powder of pigment in a synthetic resin into a granular form, and has a high matting effect. The matte can be seen from any direction. A suede-like surface can be formed.
Examples of the material of the bead pigment include Fe 2 O 3 and TiO.
2 , CaCO 3 , using a fine powder of ordinary pigment such as quinacridone, the surface of the fine powder, polyurethane, acrylic, epoxy, polyester, nylon, fluororesin, elastic resin such as vinyl chloride resin, or, If necessary, the resin may be covered with a material to which a plasticizer, a stabilizer, a surfactant or the like is added, or the pigment fine powder may be dispersed in the elastic resin.

【0014】ビーズ顔料の粒径は、形成しようとする艶
消し樹脂層の厚さによってもことなるが、粒度分布が5
〜80μmであって、且つ粒度分布の最頻出粒径10〜
35μmの範囲にあるものを用いると、特に艶消し樹脂
層がスウェード調の風合いを損なう虞れがなく、装飾層
や接着剤層の塗工性や密着性が向上するため、より好ま
しい。最も好ましいビーズ顔料としては、粒径13〜4
0μmのポリウレタン樹脂ビーズ顔料又はアクリル樹脂
ビーズ顔料等が挙げられる。また、ビーズ顔料の色は、
所望に応じて任意に選択すればよく、例えば、無色透明
なビーズ顔料を用いて、深みのある艶消し樹脂層を形成
したり、二色以上のビーズ顔料を組み合わせて、多色の
変化に富んだ艶消し樹脂層を形成することができる。
The particle size of the bead pigment varies depending on the thickness of the matting resin layer to be formed.
8080 μm and the most frequent particle size of the particle size distribution
It is more preferable to use a layer having a thickness in the range of 35 μm because the matte resin layer does not particularly impair the suede-like texture, and the coatability and adhesion of the decorative layer and the adhesive layer are improved. The most preferred bead pigments have a particle size of 13-4.
Examples include a 0 μm polyurethane resin bead pigment or an acrylic resin bead pigment. The color of the bead pigment is
It may be arbitrarily selected as desired, for example, using a colorless and transparent bead pigment, forming a deep matte resin layer, or combining two or more bead pigments, rich in multicolor variation A matte resin layer can be formed.

【0015】本発明において、意匠性を賦与するため
に、必要に応じて、絵柄層、金属蒸着層等の装飾層を設
けけることもできる。これらの層は艶消し樹脂層の表面
又は艶消し樹脂層と接着剤層との間の1層又は両層に設
ける。但し、表面に設ける場合は艶消し表面を隠蔽する
ために余白部を設ける。
In the present invention, a decorative layer such as a picture layer and a metal vapor-deposited layer can be provided, if necessary, in order to impart design properties. These layers are provided on the surface of the matte resin layer or on one or both layers between the matte resin layer and the adhesive layer. However, when it is provided on the surface, a blank portion is provided to cover the matte surface.

【0016】[0016]

【作用】本発明により、表面光沢度を変えずに耐擦傷性
も実用上殆ど劣化させず、しかも賦型フイルムを剥離す
る際に、転写層が被転写体周縁部で確実に切断されバリ
が生じない転写フイルムを供給することが可能となる。
According to the present invention, the abrasion resistance hardly deteriorates practically without changing the surface glossiness. In addition, when the imprint film is peeled off, the transfer layer is reliably cut at the peripheral edge of the transfer-receiving member to remove burrs. It is possible to supply a transfer film that does not occur.

【0017】[0017]

【実施例】以下に、実施例に基づいて、図面等を参照に
して本発明を詳細に説明する。図2は第1の実施例を示
した図である。艶消し樹脂層用の塗工液はバインダー樹
脂(熱可塑性ウレタンエラストマー)100重量部に対
してビーズ顔料(大日精化工業製:最頻出粒径23μm
のウレタン弾性ビーズ)を250重量部加えて作製した
スウェードインキに最頻出粒径0.02μm、最大粒径
0.04μmのシリカを0.25重量%添加して作製し
た。上記塗工液を厚さ25μmのコーティングマットP
ETフイルム(株式会社きもと製:離型性マット101
7−6)の表面に、ダイコートにて塗布量が乾燥時で2
5g/m2 になるように塗工して艶消し樹脂層を形成し
た。次に、この艶消し樹脂層表面に印刷インキを使用し
て絵柄をグラビア印刷し、更に接着剤(アクリルと塩化
ビニル・酢酸ビニル共重合体を重量比にして1:1で混
合した物)をダイコートにて塗布量が乾燥時で25g/
2 になるように塗工して接着層を設けて艶消し転写フ
イルムを作製した。この転写フイルムをポリスチレン
(以下PSとする)成形品にロール転写したところ、図
1(b)に示すように、膜切れ性に優れ、バリの発生が
なくなり、バリの除去工程が不要になった。従って、加
工性が良く且つ表面物性及び意匠性に優れたスウェード
調のPS成形品が得られるようになった。
DESCRIPTION OF THE PREFERRED EMBODIMENTS Hereinafter, the present invention will be described in detail based on embodiments with reference to the drawings and the like. FIG. 2 is a diagram showing the first embodiment. The coating liquid for the matte resin layer is a bead pigment (manufactured by Dainichi Seika Kogyo Co., Ltd .: most frequently used particle size: 23 μm) per 100 parts by weight of the binder resin (thermoplastic urethane elastomer).
(Urethane elastic beads) of 250 parts by weight was added to 0.25% by weight of silica having a most frequent particle size of 0.02 μm and a maximum particle size of 0.04 μm. Apply the above coating solution to a coating mat P having a thickness of 25 μm.
ET film (Kimoto Co., Ltd .: Releasable mat 101
On the surface of 7-6), the coating amount is 2
Coating was performed so as to be 5 g / m 2 to form a matte resin layer. Next, a pattern is gravure-printed on the surface of the matting resin layer using a printing ink, and an adhesive (a mixture of acrylic and vinyl chloride / vinyl acetate copolymer at a weight ratio of 1: 1) is further applied. 25 g / 25 g
m 2 and an adhesive layer was provided to prepare a matte transfer film. When this transfer film was roll-transferred to a polystyrene (hereinafter referred to as PS) molded product, as shown in FIG. 1 (b), the film was excellent in cut-off property, no burr was generated, and the burr removal step became unnecessary. . Accordingly, a swedish PS molded product having good workability and excellent surface properties and design properties can be obtained.

【0018】第2の実施例は図3に示すように、第1の
実施例で使用したPETフイルムにアクリル樹脂の剥離
層を形成した後に、第1の実施例と同様のスウェードイ
ンキを塗工して艶消し樹脂層を形成した。次に、絵柄の
印刷を行い、更に最頻出粒径0.02μm、最大粒径
0.04μmのシリカを1重量%添加した接着剤を使用
して、乾燥時の塗布量が20g/m2 になるように塗工
して艶消し転写フイルムを作製して、PS成形体に転写
を行った。その結果、第1の実施例に比較して更に膜切
れ性に優れ、且つ第1の実施例と同様に表面物性及び意
匠性に優れたスウェード調の成形品が得られた。
In the second embodiment, as shown in FIG. 3, after a release layer of an acrylic resin is formed on the PET film used in the first embodiment, the same suede ink as in the first embodiment is applied. Thus, a mat resin layer was formed. Next, a pattern is printed, and the coating amount at the time of drying is reduced to 20 g / m 2 using an adhesive containing 1% by weight of silica having a most frequent particle size of 0.02 μm and a maximum particle size of 0.04 μm. A matte transfer film was prepared by coating as described above and transferred to a PS molded body. As a result, a suede-like molded product having more excellent film-cutting properties as compared with the first example and excellent surface properties and design properties as in the first example was obtained.

【0019】[0019]

【発明の効果】本発明により、表面光沢度を変えずに耐
擦傷性も実用上殆ど劣化させず、しかも賦型フイルムを
剥離する際に、転写層が被転写体周縁部で確実に切断さ
れバリが生じない転写フイルムを供給することが可能と
なる。また、転写製品のバリの除去工程が不要となり、
作業効率の向上が図れる。
According to the present invention, the scratch resistance is practically hardly degraded without changing the surface glossiness, and the transfer layer is reliably cut at the peripheral edge of the transfer object when the imprint film is peeled off. It is possible to supply a transfer film free from burrs. Also, the step of removing burrs on the transfer product is not required,
Work efficiency can be improved.

【図面の簡単な説明】[Brief description of the drawings]

【図1】転写フイルムを転写した時バリの発生状態を示
した図
FIG. 1 is a view showing a state in which burrs are generated when a transfer film is transferred.

【図2】第1の実施例で製造した転写フイルムの構成図FIG. 2 is a configuration diagram of a transfer film manufactured in the first embodiment.

【図3】第2の実施例で製造した転写フイルムの構成図FIG. 3 is a configuration diagram of a transfer film manufactured in a second embodiment.

【符号の説明】[Explanation of symbols]

1 基材フイルム 2 転写層 3 被転写体 4 転写層のバリ 21 バインダー樹脂 22 ビーズ顔料 23 粒径0.1μm以下のシリカ 24 艶消し樹脂層 25 絵柄の印刷 26 接着剤層 31 剥離層 DESCRIPTION OF SYMBOLS 1 Base film 2 Transfer layer 3 Transfer object 4 Burr of transfer layer 21 Binder resin 22 Bead pigment 23 Silica having a particle size of 0.1 μm or less 24 Matte resin layer 25 Printing of pattern 26 Adhesive layer 31 Release layer

───────────────────────────────────────────────────── フロントページの続き (58)調査した分野(Int.Cl.7,DB名) B44C 1/165 - 1/17 ──────────────────────────────────────────────────続 き Continued on the front page (58) Field surveyed (Int.Cl. 7 , DB name) B44C 1/165-1/17

Claims (2)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】 基材フイルムの表面に転写層として少な
くとも、樹脂ビーズ顔料を含む艶消し樹脂層及び接着剤
層を積層してなる転写フイルムであって、艶消し樹脂に
粒径0.1μm以下のシリカ又は沈降性硫酸バリウムを
0.25〜0.5重量%添加して、転写層の膜切れ性を
改良したことを特徴とする艶消し転写フイルム。
1. A transfer film comprising at least a matting resin layer containing a resin bead pigment and an adhesive layer laminated on a surface of a base film as a transfer layer, wherein the matting resin has a particle size of 0.1 μm or less. A matte transfer film, characterized by adding 0.25 to 0.5% by weight of silica or precipitated barium sulfate to improve the cut-off property of the transfer layer.
【請求項2】 基材フイルムの表面に転写層として少な
くとも、樹脂ビーズ顔料を含む艶消し樹脂層及び接着剤
層を積層してなる転写フイルムであって、接着剤層に粒
径0.1μm以下のシリカ又は沈降性硫酸バリウムを1
〜2重量%添加して、転写層の膜切れ性を改良したこと
を特徴とする艶消し転写フイルム。
2. A transfer film comprising a matte resin layer containing a resin bead pigment and an adhesive layer laminated on a surface of a base film as a transfer layer, wherein the adhesive layer has a particle size of 0.1 μm or less. Of silica or precipitated barium sulfate
A matte transfer film characterized in that the addition of 〜2% by weight has improved the film breakability of the transfer layer.
JP35290192A 1992-12-14 1992-12-14 Transfer film with improved transfer layer Expired - Fee Related JP3295858B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP35290192A JP3295858B2 (en) 1992-12-14 1992-12-14 Transfer film with improved transfer layer

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP35290192A JP3295858B2 (en) 1992-12-14 1992-12-14 Transfer film with improved transfer layer

Publications (2)

Publication Number Publication Date
JPH06179283A JPH06179283A (en) 1994-06-28
JP3295858B2 true JP3295858B2 (en) 2002-06-24

Family

ID=18427229

Family Applications (1)

Application Number Title Priority Date Filing Date
JP35290192A Expired - Fee Related JP3295858B2 (en) 1992-12-14 1992-12-14 Transfer film with improved transfer layer

Country Status (1)

Country Link
JP (1) JP3295858B2 (en)

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6410469B1 (en) 1996-07-09 2002-06-25 Baker Refractories, Inc. Slagline sleeve for submerged entry nozzle and composition therefor

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JP2001089689A (en) * 1999-02-15 2001-04-03 Tosoh Corp Matting agent for printing ink, printing ink composition comprising the same and its use
JP5157218B2 (en) * 2007-03-29 2013-03-06 大日本印刷株式会社 Composite filter for display
JP5155645B2 (en) * 2007-12-10 2013-03-06 日本写真印刷株式会社 Transfer material manufacturing method and transfer material excellent in foil burr resistance
JP5685087B2 (en) * 2011-01-05 2015-03-18 株式会社きもと Blindfold film
JP2020163706A (en) * 2019-03-29 2020-10-08 大日本印刷株式会社 Transfer sheet
JP7343291B2 (en) * 2019-04-16 2023-09-12 スリーエム イノベイティブ プロパティズ カンパニー Overlaminate films and graphic laminates
CN115595056B (en) * 2022-12-15 2023-03-10 佛山市金镭科技有限公司 Alumite water-based color layer coating for realizing high-speed coating and preparation method thereof

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JPS6322697A (en) * 1986-07-16 1988-01-30 凸版印刷株式会社 Manufacture of metal evaporating transfer foil
JPH0739231B2 (en) * 1987-04-03 1995-05-01 大日本印刷株式会社 Transfer sheet
JPH0489300A (en) * 1990-07-31 1992-03-23 Dainippon Printing Co Ltd Suede pattern transfer foil
JP3023193B2 (en) * 1991-03-07 2000-03-21 大日本印刷株式会社 Matte transfer foil
JP3225411B2 (en) * 1992-09-18 2001-11-05 大日本印刷株式会社 Matte transfer foil

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6410469B1 (en) 1996-07-09 2002-06-25 Baker Refractories, Inc. Slagline sleeve for submerged entry nozzle and composition therefor
US6586355B2 (en) 1996-07-09 2003-07-01 Baker Refractories Slagline sleeve for submerged entry nozzle composition therefore

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