JP5184166B2 - Film for insert molding - Google Patents
Film for insert moldingInfo
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- JP5184166B2 JP5184166B2 JP2008075546A JP2008075546A JP5184166B2 JP 5184166 B2 JP5184166 B2 JP 5184166B2 JP 2008075546 A JP2008075546 A JP 2008075546A JP 2008075546 A JP2008075546 A JP 2008075546A JP 5184166 B2 JP5184166 B2 JP 5184166B2
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Description
本発明はインサート成型用フィルムに関する。 The present invention relates to a film for insert molding .
近年、プラスチックフィルムはその加工性、透明性等に加えて、軽量、安価といったことから、ガラスに変わり自動車業界、家電業界を始めとして種々の産業で使用されており、最近ではプラズマディスプレイ、液晶ディスプレイなどのフラットパネルディスプレイやタッチパネル、パーソナルコンピュータなどのディスプレイ用としても広く用いられている。プラスチックフィルムはガラスと比較して柔らかく、表面に傷が付き易い等の欠点を有している。この欠点を解消するために紫外線硬化型樹脂組成物をプラスチックフィルムに塗工したハードコートフィルムが用いられている。その中でもインサート成型用フィルムでは屈曲性に優れた紫外線硬化型樹脂組成物をＰＥＴフィルムに塗布、硬化し、裏面に装飾用印刷および／あるいは金属蒸着処理を施し意匠性を付与し、携帯電話等に使用されている。
従来のインサート成型用フィルムではＰＥＴフィルムの裏面の易接着層に樹脂組成物を塗布、硬化し、金属蒸着処理を施すため、蒸着処理時にかかる輻射熱によって易接着層が白化してしまう。しかしながら、表面に易接着処理を施していないＰＥＴフィルムに樹脂組成物を塗布、硬化して密着させることは困難であった。また同様に、表面に易接着処理を施していないＰＥＴフィルム上に装飾用インキや金属蒸着膜を形成させ、密着させることは困難であった。そのためＰＥＴフィルムと装飾用インキあるいは金属蒸着膜との間のプライマーとなる樹脂組成物が要求されていた。 In the conventional insert molding film, the resin composition is applied and cured on the easy-adhesion layer on the back surface of the PET film, and metal deposition is performed. Therefore, the easy-adhesion layer is whitened by the radiant heat applied during the deposition process. However, it has been difficult to apply and cure the resin composition on a PET film whose surface has not been subjected to an easy adhesion treatment. Similarly, it has been difficult to form a decorative ink or a metal vapor-deposited film on a PET film that has not been subjected to an easy adhesion treatment on the surface. Therefore, there has been a demand for a resin composition that serves as a primer between the PET film and the decorative ink or metal deposition film.
請求項１の発明は、ポリオールとポリイソシアネートを含有する熱硬化型樹脂組成物であって、前記ポリオールのガラス転移温度が７５〜９５℃かつ水酸基価が２０〜３５ｍｇＫＯＨ／ｇである熱硬化型樹脂組成物を、表面に易接着処理が施されていないＰＥＴフィルム上に塗布、硬化させて硬化被膜を形成してなることを特徴とするインサート成型用フィルム、請求項２記載の発明は、ポリオールとポリイソシアネートを含有する熱硬化型樹脂組成物であって、前記ポリオールのガラス転移温度が７５〜９５℃かつ水酸基価が２０〜３５ｍｇＫＯＨ／ｇである熱硬化型樹脂組成物を、表面に易接着処理が施されていないＰＥＴフィルム上に塗布、硬化させた硬化被膜上に装飾用印刷および／あるいは金属蒸着処理を施してなることを特徴とするインサート成型用フィルムである。 The invention of claim 1 is a thermosetting resin composition comprising a polyol and a polyisocyanate, wherein the polyol has a glass transition temperature of 75 to 95 ° C. and a hydroxyl value of 20 to 35 mgKOH / g. the composition, applied onto a PET film easy adhesion treatment is not subjected to the surface, the film for insert molding, characterized in that by forming a cured coating is cured, a second aspect of the present invention, a polyol A thermosetting resin composition containing a polyisocyanate, wherein the polyol has a glass transition temperature of 75 to 95 ° C. and a hydroxyl value of 20 to 35 mgKOH / g, and is subjected to an easy adhesion treatment on the surface. and characterized by being subjected to the coating on a PET film which have not been subjected decorative on the cured film obtained by curing the printing and / or metal deposition process That is the film for insert molding.
本発明によれば、ガラス転移温度が７５〜９５℃かつ水酸基価が２０〜３５ｍｇＫＯＨ／ｇであるポリオールとポリイソシアネートを含有する熱硬化型樹脂組成物を、表面に易接着処理を施していないＰＥＴフィルムに塗布、硬化することで密着性、耐ブロッキング性に優れたインサート成型用フィルムを得ることができ、さらにその硬化被膜上に装飾用印刷および／あるいは金属蒸着処理を施すことが可能である。 According to the present invention, a thermosetting resin composition containing a polyol and a polyisocyanate having a glass transition temperature of 75 to 95 ° C. and a hydroxyl value of 20 to 35 mg KOH / g is not subjected to easy adhesion treatment on the surface. By applying and curing to the film, an insert molding film having excellent adhesion and blocking resistance can be obtained, and further, decorative printing and / or metal deposition treatment can be performed on the cured film.
以下、本発明について詳細に説明する。本発明に用いるガラス転移温度（以下Ｔｇ）が７５〜９５℃かつ水酸基価（以下ＯＨ価）が２０〜３５ｍｇＫＯＨ／ｇであるポリオールとしては、ポリエーテルポリオール、ポリエステルポリオール、アクリルポリオール、エポキシポリオール、カーボネートポリオール、カプロラクトンポリオールなどが挙げられる。 Hereinafter, the present invention will be described in detail. Examples of the polyol having a glass transition temperature (hereinafter referred to as Tg) of 75 to 95 ° C. and a hydroxyl value (hereinafter referred to as OH number) of 20 to 35 mgKOH / g used in the present invention include polyether polyol, polyester polyol, acrylic polyol, epoxy polyol, and carbonate. A polyol, a caprolactone polyol, etc. are mentioned.
市販品としてはＶＵ−１９１（大日本インキ化学工業株式会社製、Ｔｇ９４℃、ＯＨ価３３ｍｇＫＯＨ／ｇ）、Ｑ１９５−４５（三井化学株式会社製、Ｔｇ８４℃、ＯＨ価２７ｍｇＫＯＨ／ｇ）、Ｑ６１２（三井化学株式会社製、Ｔｇ７９℃、ＯＨ価２５ｍｇＫＯＨ／ｇ）等が挙げられる。 Commercially available products include VU-191 (Dainippon Ink and Chemicals, Tg 94 ° C., OH value 33 mgKOH / g), Q195-45 (Mitsui Chemicals, Tg 84 ° C., OH value 27 mgKOH / g), Q612 (Mitsui Chemical Co., Ltd., Tg 79 ° C., OH value 25 mg KOH / g) and the like.
ポリオールのガラス転移温度が７５℃よりも低い場合、硬化被膜の硬度が不十分であるため、フィルム巻き取り時に擦れ傷やブロッキングが発生する。９５℃よりも高い場合、硬化被膜が硬すぎて脆くなり、ＰＥＴフィルムとの密着性が低下する。またポリオールの水酸基価が２０ｍｇＫＯＨ／ｇよりも低い場合、ポリイソシアネートとの反応性が悪く、硬化不良により十分な硬度が得られず、前記、ガラス転移温度が７５℃よりも低い場合と同様、フィルム巻き取り時に擦れ傷やブロッキングが発生する。３５ｍｇＫＯＨ／ｇよりも高い場合、ポリイソシアネートとより密な架橋構造を形成し、硬化収縮により密着性が低下する。 When the glass transition temperature of the polyol is lower than 75 ° C., the cured film has insufficient hardness, and thus scratches and blocking occur during film winding. When it is higher than 95 ° C., the cured film is too hard and brittle, and the adhesion with the PET film is lowered. Also, when the hydroxyl value of the polyol is lower than 20 mgKOH / g, the reactivity with the polyisocyanate is poor and sufficient hardness cannot be obtained due to poor curing, as in the case where the glass transition temperature is lower than 75 ° C. Scratches and blocking occur during winding. When it is higher than 35 mgKOH / g, it forms a denser cross-linked structure with polyisocyanate, and the adhesiveness decreases due to curing shrinkage.
ポリイソシアネートとしては、特に限定されることなく、本発明に用いるポリイソシアネート化合物としては、具体的には、例えばジフェニルメタンジイソシアネート（ＭＤＩ）、トリレンジイソシアネート（ＴＤＩ）、ナフタレンジイソシアネート等の芳香族ポリイソシアネート類のほか、ヘキサメチレンジイソシアネート（ＨＤＩ）、リジンメチルエステルジイソシアネート等の脂肪族ポリイソシアネート類、水添ジフェニルメタンジイソシアネート、イソホロンジイソシアネート、ノルボルナンジイソシアネート、水添トリレンジイソシアネート等の脂環式ポリイソシアネート類が挙げられる。 The polyisocyanate is not particularly limited, and specific examples of the polyisocyanate compound used in the present invention include aromatic polyisocyanates such as diphenylmethane diisocyanate (MDI), tolylene diisocyanate (TDI), and naphthalene diisocyanate. In addition, aliphatic polyisocyanates such as hexamethylene diisocyanate (HDI) and lysine methyl ester diisocyanate, and alicyclic polyisocyanates such as hydrogenated diphenylmethane diisocyanate, isophorone diisocyanate, norbornane diisocyanate, and hydrogenated tolylene diisocyanate can be mentioned.
市販品としてはＤＮ−９８１（大日本インキ化学株式会社製）Ｄ−１２０Ｎ、Ｄー１７０Ｎ、Ｄ−１７７Ｎ（三井武田ケミカル株式会社製）、コロネートＨＸ（日本ポリウレタン工業株式会社製）等が挙げられる。 Examples of commercially available products include DN-981 (Dainippon Ink Chemical Co., Ltd.) D-120N, D-170N, D-177N (Mitsui Takeda Chemical Co., Ltd.), Coronate HX (Nihon Polyurethane Industry Co., Ltd.), and the like. .
この他に有機溶剤を添加することもできる。有機溶剤としては、例えば、ヘキサン、ヘプタン、シクロヘキサンなどの脂肪族炭化水素系、トルエン、キシレンなどの芳香族炭化水素系、塩化メチレン、塩化エチレンなどのハロゲン化炭化水素系、メタノール、エタノール、プロパノール、ブタノールなどのアルコール系、アセトン、メチルエチルケトン、メチルイソブチルケトン、２−ペンタノン、イソホロンなどのケトン系、酢酸エチル、酢酸ブチルなどのエステル系、エチルセロソルブなどのセロソルブ系溶剤などが挙げられる。 In addition, an organic solvent can be added. Examples of the organic solvent include aliphatic hydrocarbons such as hexane, heptane and cyclohexane, aromatic hydrocarbons such as toluene and xylene, halogenated hydrocarbons such as methylene chloride and ethylene chloride, methanol, ethanol, propanol, Examples include alcohols such as butanol, ketones such as acetone, methyl ethyl ketone, methyl isobutyl ketone, 2-pentanone and isophorone, esters such as ethyl acetate and butyl acetate, and cellosolve solvents such as ethyl cellosolve.
その他、各種添加剤、例えば、反応促進剤、酸化防止剤、レベリング剤、消泡剤、無機充填剤、カップリング剤、防腐剤、可塑剤、流動調整剤、増粘剤、ｐＨ調整剤等などを配合材料としてもよい。 Other additives such as reaction accelerators, antioxidants, leveling agents, antifoaming agents, inorganic fillers, coupling agents, preservatives, plasticizers, flow regulators, thickeners, pH adjusters, etc. May be used as a blending material.
本発明の熱硬化型樹脂組成物のＰＥＴフィルムへの塗布方法については特に制限はなく、公知の方法、例えばグラビアコート法、バーコート法、ナイフコート法、ロールコート法、ブレードコート法、ダイコート法、スプレーコート法、ディッピング法などを用いることができ、乾燥後塗膜の厚みを２００ｎｍ〜１μｍとすることが好ましい。硬化被膜層の厚みが２００ｎｍ未満であると、十分な硬度が発現せず、フィルム巻き取り時に擦れ傷やブロッキングが発生し、１μｍを超えると密着性の劣化や成型時にクラックが発生するため好ましくない。 The method for applying the thermosetting resin composition of the present invention to the PET film is not particularly limited, and known methods such as a gravure coating method, a bar coating method, a knife coating method, a roll coating method, a blade coating method, and a die coating method. A spray coating method, a dipping method, or the like can be used, and the thickness of the coating film after drying is preferably 200 nm to 1 μm. If the thickness of the cured coating layer is less than 200 nm, sufficient hardness will not be exhibited, and scratches and blocking will occur when the film is wound, and if it exceeds 1 μm, adhesion will deteriorate and cracks will occur during molding. .
本発明の熱硬化型樹脂組成物を表面に塗布、硬化させたインサート成型用フィルムに金属蒸着処理により被膜形成可能な金属薄膜としてはアルミニウム、錫、亜鉛、金、銀、白金、ニッケルなどが挙げられる。 Examples of the metal thin film capable of forming a film by metal vapor deposition on the film for insert molding applied and cured on the surface of the thermosetting resin composition of the present invention include aluminum, tin, zinc, gold, silver, platinum, nickel and the like. It is done.
本発明の熱硬化型樹脂組成物を表面に塗布、硬化させたインサート成型用フィルムに印刷処理により被膜形成可能なインキとしては特に限定されることなく、例えば市販品としてはＩＰＸ−９７１、ＩＰＸ−１０２、ＩＰＸ−０００（帝国インキ製造株式会社製）、ＪＴ−２５（株式会社セイコーアドバンス製）などが挙げられる。印刷の方法としては特に限定されることなく、スクリーン印刷、インクジェット印刷、オフセット印刷、グラビア印刷、ホットスタンプ印刷などが挙げられる。 There are no particular limitations on the ink that can be formed into a film by printing on an insert molding film that has been coated and cured with the thermosetting resin composition of the present invention. For example, IPX-971, IPX- 102, IPX-000 (made by Teikoku Ink Manufacturing Co., Ltd.), JT-25 (made by Seiko Advance Co., Ltd.), and the like. The printing method is not particularly limited, and includes screen printing, ink jet printing, offset printing, gravure printing, hot stamp printing, and the like.
以下、本発明について実施例、比較例を挙げてより詳細に説明するが、具体例を示すものであって特にこれらに限定するものではない。 EXAMPLES Hereinafter, although an Example and a comparative example are given and demonstrated in detail about this invention, a specific example is shown and it does not specifically limit to these.
アクリルポリオール（ＶＵ−１９１、大日本インキ化学工業株式会社製、固形分５５％、Ｔｇ９４℃、ＯＨ価３３ｍｇＫＯＨ／ｇ）１００重量部、脂肪族系イソシアネート化合物（ＤＮ−９８１、大日本インキ化学株式会社製、固形分７５％）１８重量部、溶媒としてＭＥＫを用い固形分５％の熱硬化型樹脂組成物を得た。 Acrylic polyol (VU-191, manufactured by Dainippon Ink & Chemicals, Inc., solid content 55%, Tg 94 ° C., OH value 33 mgKOH / g) 100 parts by weight, aliphatic isocyanate compound (DN-981, Dainippon Ink & Chemicals, Inc.) Manufactured, 75% solid content) 18 parts by weight, using MEK as a solvent, a 5% solid content thermosetting resin composition was obtained.
アクリルポリオール（Ｑ１９５−４５、三井化学株式会社製、固形分４５％、Ｔｇ８４℃、ＯＨ価２７ｍｇＫＯＨ／ｇ）１００重量部、ＤＮ−９８１（大日本インキ化学株式会社製、固形分７５％）１５重量部、溶媒としてＭＥＫを用い固形分５％の熱硬化型樹脂組成物を得た。 Acrylic polyol (Q195-45, Mitsui Chemicals, solid content 45%, Tg 84 ° C., OH value 27 mg KOH / g) 100 parts by weight, DN-981 (Dainippon Ink Chemical Co., Ltd., solid content 75%) 15 weight A thermosetting resin composition having a solid content of 5% was obtained using MEK as a part and a solvent.
アクリルポリオール（Ｑ６１２、三井化学株式会社製、固形分５０％、Ｔｇ７９℃、ＯＨ価２５ｍｇＫＯＨ／ｇ）１００重量部、ＤＮ−９８１（大日本インキ化学株式会社製、固形分７５％）１４重量部、溶媒としてＭＥＫを用い固形分５％の熱硬化型樹脂組成物を得た。 Acrylic polyol (Q612, manufactured by Mitsui Chemicals, solid content 50%, Tg 79 ° C., OH value 25 mgKOH / g) 100 parts by weight, DN-981 (Dainippon Ink Chemical Co., Ltd., solid content 75%) 14 parts by weight, A thermosetting resin composition having a solid content of 5% was obtained using MEK as a solvent.
比較例１
アクリルポリオール（Ｑ１６６、三井化学株式会社製、固形分５０％、Ｔｇ５３℃、ＯＨ価３０ｍｇＫＯＨ／ｇ）１００重量部、ＤＮ−９８１（大日本インキ化学株式会社製、固形分７５％）１７重量部、溶媒としてＭＥＫを用い固形分５％の熱硬化型樹脂組成物を得た。
Comparative Example 1
Acrylic polyol (Q166, manufactured by Mitsui Chemicals, solid content 50%, Tg 53 ° C., OH value 30 mg KOH / g) 100 parts by weight, DN-981 (Dainippon Ink Chemical Co., Ltd., solid content 75%) 17 parts by weight, A thermosetting resin composition having a solid content of 5% was obtained using MEK as a solvent.
比較例２
アクリルポリオール（Ｑ１６４、三井化学株式会社製、固形分４５％、Ｔｇ９８℃、ＯＨ価２７ｍｇＫＯＨ／ｇ）１００重量部、ＤＮ−９８１（大日本インキ化学株式会社製、固形分７５％）１５重量部、溶媒としてＭＥＫを用い固形分５％の熱硬化型樹脂組成物を得た。
Comparative Example 2
Acrylic polyol (Q164, manufactured by Mitsui Chemicals, solid content 45%, Tg 98 ° C., OH value 27 mg KOH / g) 100 parts by weight, DN-981 (Dainippon Ink Chemical Co., Ltd., solid content 75%) 15 parts by weight, A thermosetting resin composition having a solid content of 5% was obtained using MEK as a solvent.
比較例３
アクリルポリオール（ＷＸＵ−８８０、大日本インキ化学工業株式会社製、固形分５０％、Ｔｇ９０℃、ＯＨ価１０ｍｇＫＯＨ／ｇ）１００重量部、ＤＮ−９８１（大日本インキ化学株式会社製、固形分７５％）６重量部、溶媒としてＭＥＫを用い固形分５％の熱硬化型樹脂組成物を得た。
Comparative Example 3
Acrylic polyol (WXU-880, manufactured by Dainippon Ink Chemical Co., Ltd., solid content 50%, Tg 90 ° C., OH value 10 mg KOH / g) 100 parts by weight, DN-981 (Dainippon Ink Chemical Co., Ltd., solid content 75% ) 6 parts by weight, MEK was used as a solvent to obtain a thermosetting resin composition having a solid content of 5%.
比較例４
アクリルポリオール（Ｑ１７４、三井化学株式会社製、固形分５０％、Ｔｇ８５℃、ＯＨ価４５ｍｇＫＯＨ／ｇ）１００重量部、ＤＮ−９８１（大日本インキ化学株式会社製、固形分７５％）２５重量部、溶媒としてＭＥＫを用い固形分５％の熱硬化型樹脂組成物を得た。
Comparative Example 4
Acrylic polyol (Q174, manufactured by Mitsui Chemicals, solid content 50%, Tg 85 ° C., OH value 45 mg KOH / g) 100 parts by weight, DN-981 (Dainippon Ink Chemical Co., Ltd., solid content 75%) 25 parts by weight, A thermosetting resin composition having a solid content of 5% was obtained using MEK as a solvent.
実施例、比較例で作製した熱硬化型樹脂組成物を、易接着処理を施していないＰＥＴフィルムに硬化膜厚が５００ｎｍとなるようにバーコート法で塗工して熱風乾燥機で１１０℃、３分の条件で乾燥してそれぞれインサート成型用フィルムを得た。
評価結果を表１に示す。
The thermosetting resin compositions prepared in Examples and Comparative Examples were applied to a PET film not subjected to an easy adhesion treatment by a bar coating method so that the cured film thickness was 500 nm, and 110 ° C. with a hot air dryer. Each film was dried for 3 minutes to obtain an insert molding film.
The evaluation results are shown in Table 1.
試験・評価方法
（１）耐スチールウール性
＃００００スチールウールによる表面摩擦試験（荷重５０ｇｆ、ストローク幅３０ｍｍ、１０往復）後に傷の有無を目視観察により評価。○：傷０本、×：傷１本以上。
（２）密着性
ＪＩＳ Ｋ ５６００−５−６（１９９９年版）に基づく碁盤目試験に基づき、塗工面に１０×１０にマス目を作成し、セロハンテープを貼り、上方に引っ張り剥離状況を確認。剥がれなかったマス目を数える。
（３）耐ブロッキング性
塗膜にＰＥＴフィルムを被せ、その上に１ｋｇの重りを乗せて熱風乾燥機で８０℃、３０分の条件で放置後、ブロッキングの有無を確認。
（４）インキ密着性
塗膜上にＩＰＸ−９７１（帝国インキ製造株式会社）１００重量部と２２０硬化剤（帝国インキ製造株式会社）１５部を混合して得たインキをブレードコート法により１５μｍ塗工し、熱風乾燥機で９０℃、６０分の条件で乾燥し、（２）と同様に密着性を確認。
（５）アルミニウム蒸着密着性
塗膜上に蒸着装置によりアルミニウム薄膜を形成し、（２）と同様に密着性を確認。
Test / Evaluation Method (1) Resistance to steel wool # 0000 After surface friction test with steel wool (load 50 gf, stroke width 30 mm, 10 reciprocations), the presence or absence of scratches was evaluated by visual observation. ○: No scratch, ×: One or more scratches.
(2) Adhesion Based on a cross-cut test based on JIS K 5600-5-6 (1999 edition), 10 × 10 squares were created on the coated surface, cellophane tape was applied, and the tensile peeling condition was confirmed upward. Count squares that did not peel off.
(3) Blocking resistance A PET film was placed on the coating film, and a 1 kg weight was placed on the coating film. After standing in a hot air dryer at 80 ° C. for 30 minutes, the presence or absence of blocking was confirmed.
(4) Ink adhesion An ink obtained by mixing 100 parts by weight of IPX-971 (Imperial Ink Manufacturing Co., Ltd.) and 15 parts of 220 curing agent (Imperial Ink Manufacturing Co., Ltd.) on the coating film was applied by a blade coating method to a thickness of 15 μm. And dried in a hot air dryer at 90 ° C. for 60 minutes, confirming adhesion as in (2).
(5) Aluminum vapor deposition adhesiveness An aluminum thin film was formed on the coating film with a vapor deposition device, and the adhesion was confirmed in the same manner as in (2).
Claims (2)
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Cited By (1)
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| CN105462467A (en) * | 2014-09-30 | 2016-04-06 | 荒川化学工业株式会社 | Undercoat for plastic with aluminum film, plastic and plastic film with aluminum film, decorative film used for in-mold forming, and decorative film used for insert molding |
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| JP5641321B2 (en) * | 2009-11-30 | 2014-12-17 | 荒川化学工業株式会社 | Undercoat agent for plastic with inorganic thin film, plastic with inorganic thin film, and decorative film for in-mold or insert molding |
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| JPS6128518A (en) * | 1984-07-20 | 1986-02-08 | Asahi Chem Ind Co Ltd | Production of prepolymer for ductile polyurethane coating |
| JP2001026749A (en) * | 1999-03-03 | 2001-01-30 | Kansai Paint Co Ltd | Overcoating composition and laminated film for adhesion |
| CN101636268B (en) * | 2007-03-30 | 2014-10-29 | 木本股份有限公司 | Film for insert molding and resin molded article using the same |
| JP4790065B2 (en) * | 2007-07-11 | 2011-10-12 | 株式会社きもと | Resin molded product using insert molding film |
| JP2009083150A (en) * | 2007-09-27 | 2009-04-23 | Kimoto & Co Ltd | Flame retardant sheet |
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| CN105462467A (en) * | 2014-09-30 | 2016-04-06 | 荒川化学工业株式会社 | Undercoat for plastic with aluminum film, plastic and plastic film with aluminum film, decorative film used for in-mold forming, and decorative film used for insert molding |
| CN105462467B (en) * | 2014-09-30 | 2019-01-08 | 荒川化学工业株式会社 | Plastics priming paint with aluminium film, the plastics with aluminium film and plastic foil in-molded with decorating film and be insert molded and use decorating film |
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