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TWI294351B - Laminate containing 4-methyl-1-pentene based polymer and release film comprising the same - Google Patents

Laminate containing 4-methyl-1-pentene based polymer and release film comprising the same Download PDF

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Publication number
TWI294351B
TWI294351B TW095116834A TW95116834A TWI294351B TW I294351 B TWI294351 B TW I294351B TW 095116834 A TW095116834 A TW 095116834A TW 95116834 A TW95116834 A TW 95116834A TW I294351 B TWI294351 B TW I294351B
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Taiwan
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layer
surface layer
mass
copolymer
resin
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TW095116834A
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Chinese (zh)
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TW200706364A (en
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Yusuke Mishiro
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Mitsui Chemicals Inc
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    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B27/00Layered products comprising a layer of synthetic resin
    • B32B27/32Layered products comprising a layer of synthetic resin comprising polyolefins
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B27/00Layered products comprising a layer of synthetic resin
    • B32B27/06Layered products comprising a layer of synthetic resin as the main or only constituent of a layer, which is next to another layer of the same or of a different material
    • B32B27/08Layered products comprising a layer of synthetic resin as the main or only constituent of a layer, which is next to another layer of the same or of a different material of synthetic resin
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B27/00Layered products comprising a layer of synthetic resin
    • B32B27/34Layered products comprising a layer of synthetic resin comprising polyamides
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B27/00Layered products comprising a layer of synthetic resin
    • B32B27/42Layered products comprising a layer of synthetic resin comprising condensation resins of aldehydes, e.g. with phenols, ureas or melamines
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B7/00Layered products characterised by the relation between layers; Layered products characterised by the relative orientation of features between layers, or by the relative values of a measurable parameter between layers, i.e. products comprising layers having different physical, chemical or physicochemical properties; Layered products characterised by the interconnection of layers
    • B32B7/04Interconnection of layers
    • B32B7/06Interconnection of layers permitting easy separation
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B7/00Layered products characterised by the relation between layers; Layered products characterised by the relative orientation of features between layers, or by the relative values of a measurable parameter between layers, i.e. products comprising layers having different physical, chemical or physicochemical properties; Layered products characterised by the interconnection of layers
    • B32B7/04Interconnection of layers
    • B32B7/12Interconnection of layers using interposed adhesives or interposed materials with bonding properties
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L23/00Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
    • C08L23/02Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
    • C08L23/18Homopolymers or copolymers of hydrocarbons having four or more carbon atoms
    • C08L23/20Homopolymers or copolymers of hydrocarbons having four or more carbon atoms having four to nine carbon atoms
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J123/00Adhesives based on homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Adhesives based on derivatives of such polymers
    • C09J123/02Adhesives based on homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Adhesives based on derivatives of such polymers not modified by chemical after-treatment
    • C09J123/04Homopolymers or copolymers of ethene
    • C09J123/08Copolymers of ethene
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J123/00Adhesives based on homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Adhesives based on derivatives of such polymers
    • C09J123/02Adhesives based on homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Adhesives based on derivatives of such polymers not modified by chemical after-treatment
    • C09J123/18Homopolymers or copolymers of hydrocarbons having four or more carbon atoms
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J123/00Adhesives based on homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Adhesives based on derivatives of such polymers
    • C09J123/02Adhesives based on homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Adhesives based on derivatives of such polymers not modified by chemical after-treatment
    • C09J123/18Homopolymers or copolymers of hydrocarbons having four or more carbon atoms
    • C09J123/20Homopolymers or copolymers of hydrocarbons having four or more carbon atoms having four to nine carbon atoms
    • HELECTRICITY
    • H05ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
    • H05KPRINTED CIRCUITS; CASINGS OR CONSTRUCTIONAL DETAILS OF ELECTRIC APPARATUS; MANUFACTURE OF ASSEMBLAGES OF ELECTRICAL COMPONENTS
    • H05K3/00Apparatus or processes for manufacturing printed circuits
    • H05K3/02Apparatus or processes for manufacturing printed circuits in which the conductive material is applied to the surface of the insulating support and is thereafter removed from such areas of the surface which are not intended for current conducting or shielding
    • H05K3/022Processes for manufacturing precursors of printed circuits, i.e. copper-clad substrates
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2250/00Layers arrangement
    • B32B2250/24All layers being polymeric
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2307/00Properties of the layers or laminate
    • B32B2307/30Properties of the layers or laminate having particular thermal properties
    • B32B2307/306Resistant to heat
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2307/00Properties of the layers or laminate
    • B32B2307/40Properties of the layers or laminate having particular optical properties
    • B32B2307/402Coloured
    • B32B2307/4023Coloured on the layer surface, e.g. ink
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2307/00Properties of the layers or laminate
    • B32B2307/50Properties of the layers or laminate having particular mechanical properties
    • B32B2307/538Roughness
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2307/00Properties of the layers or laminate
    • B32B2307/50Properties of the layers or laminate having particular mechanical properties
    • B32B2307/546Flexural strength; Flexion stiffness
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2307/00Properties of the layers or laminate
    • B32B2307/50Properties of the layers or laminate having particular mechanical properties
    • B32B2307/56Damping, energy absorption
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2307/00Properties of the layers or laminate
    • B32B2307/70Other properties
    • B32B2307/748Releasability
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2451/00Decorative or ornamental articles
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2457/00Electrical equipment
    • B32B2457/08PCBs, i.e. printed circuit boards
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L23/00Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
    • C08L23/02Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
    • HELECTRICITY
    • H05ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
    • H05KPRINTED CIRCUITS; CASINGS OR CONSTRUCTIONAL DETAILS OF ELECTRIC APPARATUS; MANUFACTURE OF ASSEMBLAGES OF ELECTRICAL COMPONENTS
    • H05K1/00Printed circuits
    • H05K1/02Details
    • H05K1/03Use of materials for the substrate
    • H05K1/0393Flexible materials

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Manufacturing & Machinery (AREA)
  • Microelectronics & Electronic Packaging (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Laminated Bodies (AREA)
  • Non-Metallic Protective Coatings For Printed Circuits (AREA)
  • Adhesives Or Adhesive Processes (AREA)

Description

1294351 九、發明說明: 【發明所屬之技術領域】 •本發=係關於含有4-甲基一丨—戊烯系聚合體之積層體及 、其所传之離型膜。更詳言之,係關於將膜或片狀之積層 物加ί及加壓成形時所使用之離型膜用積層體,特別係關 於在製造可撓性印刷電路基板時,被使用作為將屬於保護 二:(銅’自)面之保濩層的覆蓋層(cover〗ay)膜,藉由接 癱著劑進行加熱及加壓而接著時所使用的離型膜,並兼具適 鲁度緩衝性與優越離型性之積層體及由此積層體所得之可 撓性印刷電路基板製造用離型膜。 【先前技術】 於製造可撓性印刷電路基板(以下稱為rFpc」)的情況 :,一般己知係於形成有電路之基板上設置覆蓋層。此覆 盍層在印刷電路僅形成於基板單面上之單面型的情況 下,僅於單面上使用熱硬化型接著劑進行加熱及加壓而將 鲁復盘層接著’而在於基板兩面或多層上相互設置印刷電路 的情況下,於兩面上使用熱硬化型接著劑進行加熱及加壓 •而將覆蓋層接著。 、 形成有電路之基板與覆蓋層的接著,係使用熱硬化型接 -著劑’將形成有電路之基板與覆蓋層夾在金覆板中加熱及 〜加壓而進行,但為了避免在加熱及加壓時覆蓋層與金屬板 發生接著的事態,於其中間係使用聚四氟乙烯、四氟乙烯 一六氟丙烯共聚合體、及聚氟乙烯等之氟系膜或聚曱基戊 烯膜等之離型膜。 312XP/發發明說明書(補件)/95-09/95116834 5 ⑧ 1294351 八另外’ FPC中,用於與其他零件進行電性連接的端子部 $上並未進行覆蓋層的被覆,連接部分的電路呈露出狀 匕而在將露出部分以外以覆蓋層被覆的情況下,塗佈於 覆蓋層的接著劑,將因為在形成有電路之基板上接^覆苗 層時的加熱及加壓而熔融,而屢屢流出至此露出部分= 路表面上,使電路表面被接著劑的層所覆蓋,其 電性連接不良的現象。 、曰 /為了解決此種問題,對於製造FPC時所使用的離型膜, 係訴求良好離型性,以及藉由跟隨覆蓋層或Fpc表面的凹 凸,以防止接著劑由覆蓋層之端面流出至電路上, 的緩衝性。 汁0月 專利文獻1中,揭示有將軟質聚烯烴層作為中間層,於 其内外兩面上形成結晶性聚甲基戊烯層之離型臈。a 、 另外,專利文獻2中,揭示有表面層屬於聚4 -曱基一 1一 戊烯,經由接著層乙烯•丙烯橡膠,使聚乙烯、聚^烯、 乙烯•丙烯酸酯共聚合體、乙烯•曱基丙烯酸酯共聚合體 響或乙烯-醋酸乙烯酯共聚合體等之樹脂進行積層之=層 •膜。然而,此等離型膜及多層膜,因為屬於軟質聚烯烴層 、的聚乙烯和聚丙烯的熔點較低,在製造FPC時作為離型^ •而重疊於覆蓋層上進行加熱及加壓時,屬於軟質聚烯烴層 、的聚乙烯和聚丙烯將從離型膜及多層膜的端部超出而^ 著於形成有電路之基板面和使用於加熱及加壓的金屬 板,而有FPC製造產率降低和作業效率降低的問題。另 外’專利文獻1的離型膜因為不具有接著層,故更容易發 312XP/發發明說明書(補件)/95-09/95116834 6 1294351 生軟質聚嫦經層的超出’專利文獻2中使用於接著層的乙 埽•丙浠橡膠,因為溶融黏度較表面層之聚4 一甲基—1 一戍 烯來得高,故有多層膜之厚薄精度差劣、生產性降低之問 題。 另外,專利文獻3中揭示有一種離型膜,係以由表面侧 依序積層聚4-曱基-1-戊烯樹脂層、接著性樹脂層、耐熱 性樹脂層之3層膜,或以耐熱性樹脂層為中心,於其兩側 積層有接著性樹脂層及聚4-甲基-卜戊烯樹脂層之5層 膜。然而,此離型膜中,因為使用於耐熱性樹脂層之樹脂 屬於在4.6(kg/cm2)荷重下所測定之熱變形溫度為13〇t: 以上,且溫度140°C下之降伏點應力為1〇〇(kg/cm2)以上 之極不易熱變形的高硬度樹脂,故於製造Fpc時,依形成 有電路之基板、覆蓋層膜、離型膜的順序重疊並加熱及加 壓時,離型膜將無法追隨形成有電路之基板的凹凸,而有 形成有電路之基板與覆蓋層膜之間的接著劑流出至Fpc 電路面上的問題。1294351 IX. Description of the Invention: [Technical Field of the Invention] The present invention relates to a laminate comprising a 4-methyl fluorene-pentene polymer and a release film thereof. More specifically, the laminated body for a release film which is used for the film or sheet laminate and the pressure molding, in particular, when used in the manufacture of a flexible printed circuit board, is used as Protection 2: The cover layer (cover ay) film of the (copper 'self') surface, which is heated and pressurized by an adhesive, and then the release film used, and has a suitable degree A release film having a cushioning property and a superior release property, and a release film for producing a flexible printed circuit board obtained by the laminate. [Prior Art] In the case of manufacturing a flexible printed circuit board (hereinafter referred to as "rFpc"), it is generally known to provide a cover layer on a substrate on which a circuit is formed. In the case where the printed circuit is formed on only one side of the substrate, the heat-curing type adhesive is used for heating and pressurization on only one side, and the ruthenium layer is followed by 'on both sides of the substrate. In the case where a printed circuit is provided on each other in a plurality of layers, heat and pressure are applied to both surfaces using a heat-curable adhesive, and the cover layer is subsequently attached. The substrate and the cover layer on which the circuit is formed are subsequently heated and pressed by sandwiching the circuit-formed substrate and the cover layer with a thermosetting type bonding agent, but in order to avoid heating And a state in which the coating layer and the metal sheet are followed by the pressurization, and a fluorine-based film or a polydecylpentene film of polytetrafluoroethylene, tetrafluoroethylene-hexafluoropropylene copolymer, and polyvinyl fluoride is used in the middle thereof. Wait for the release film. 312XP/Inventive Manual (Supplement)/95-09/95116834 5 8 1294351 八In the other 'FPC, the terminal part $ for electrical connection with other parts is not covered with a cover layer, and the circuit of the connection part When the exposed layer is covered with a coating layer other than the exposed portion, the adhesive applied to the coating layer is melted by heating and pressurization when the seed layer is formed on the substrate on which the circuit is formed. However, it is often discharged to the exposed portion = the surface of the road, so that the surface of the circuit is covered by the layer of the adhesive, and the electrical connection is poor.曰/ In order to solve this problem, the release film used in the manufacture of FPC is intended to have good release properties, and to prevent the adhesive from flowing out from the end face of the cover layer by following the irregularities of the cover layer or the surface of the Fpc. On the circuit, the cushioning. Juice 0. Patent Document 1 discloses a release enthalpy in which a soft polyolefin layer is used as an intermediate layer to form a crystalline polymethylpentene layer on both inner and outer surfaces thereof. a, in addition, in Patent Document 2, it is disclosed that the surface layer belongs to poly-4-indolyl-1-pentene, and polyethylene, poly(ethylene oxide), ethylene acrylate copolymer, ethylene, and the like are provided via an adhesive layer of ethylene/propylene rubber. A layered film is formed by a resin such as a mercapto acrylate copolymer or an ethylene-vinyl acetate copolymer. However, such a release film and a multilayer film have a low melting point of polyethylene and polypropylene which are soft polyolefin layers, and are used as a release type in the production of FPC, and are superposed on the cover layer for heating and pressurization. Polyethylene and polypropylene, which are soft polyolefin layers, will extend from the ends of the release film and the multilayer film to the surface of the substrate on which the circuit is formed and the metal plate used for heating and pressurization, and are manufactured by FPC. The problem of reduced yield and reduced work efficiency. In addition, the release film of the patent document 1 is more likely to be used in the patent document 2 because it does not have an adhesive layer, so it is easier to send the 312XP/inventive specification (supplement)/95-09/95116834 6 1294351. In the adhesive layer of the acetamidine-propene rubber, since the melt viscosity is higher than that of the surface layer of polymethyl 4-methyl-1-decene, there is a problem that the thickness and thickness of the multilayer film are inferior and the productivity is lowered. Further, Patent Document 3 discloses a release film in which a 3-layer film of a polyfluorenyl 4-pentene resin layer, an adhesive resin layer, and a heat resistant resin layer is sequentially laminated from the surface side, or The heat resistant resin layer is centered, and a five-layer film of an adhesive resin layer and a poly-4-methyl-p-pentene resin layer is laminated on both sides. However, in this release film, since the resin used for the heat resistant resin layer belongs to a heat distortion temperature measured at a load of 4.6 (kg/cm 2 ) of 13 〇 t: or more, and a stress at a temperature of 140 ° C It is a high-hardness resin which is extremely hard to be thermally deformed at a temperature of 1 〇〇 (kg/cm 2 ) or more. Therefore, when FPC is manufactured, when a circuit-formed substrate, a cover film, and a release film are stacked in this order, and heated and pressurized, The release film will not follow the irregularities of the substrate on which the circuit is formed, and there is a problem that the adhesive between the substrate on which the circuit is formed and the cover film flow out onto the Fpc circuit surface.

甲基1戊烯糸聚合體樹脂予以被覆者 另外:專利文獻4中揭示有—種印刷電路基板製造用離 ,膜係外層為4H卜戊烯系聚合體樹脂,内層為特 =之聚烯㈣樹脂,且於該内層上下具有該外層的多層樹 脂=為了不使内層超出’將内層之周圍以屬於外層之 〇 —— =度係依FPC種類而異,因此,藉由裁切積層體而使用 二二Γΐ度的離型膜'然而,現實方面難以配合各式各 私的見度而以外層被覆内層,其步驟將變得複雜而使The methyl 1 pentene fluorene polymer resin is coated. In addition, Patent Document 4 discloses a method for producing a printed circuit board, wherein the outer layer of the film is a 4H pentene polymer resin, and the inner layer is a poly olefin (4). Resin, and the multilayer resin having the outer layer above and below the inner layer = in order not to make the inner layer beyond 'the inner layer is surrounded by the outer layer - the degree varies depending on the type of FPC, and therefore, by cutting the laminated body Two-two-degree release film' However, in reality, it is difficult to match various private views and the outer layer is covered with the inner layer, and the steps will become complicated.

般而言,FPC 312ΧΡ/發翻說明書(補件)/95-09/95116834 7 1294351 生產性顯著降低。再者,雖提案有吹氣成形法作為製造方 =,但因為配合離型膜的寬度必需變更圓型模具的大小和 、恥脹比,又各層的厚度難以變得均勻,故製造FPC時進行 =熱及加壓時,離型膜表面將發生皺摺,在發生皺摺的部 刀離型膜將無法充分追隨形成有電路之基板面的凹凸, 而產生空陽:,或皺摺轉印i FPC ±,故有無法得到具有可 充分滿足之外觀的FPC之問題。 、另外,專利文獻5揭示一種積層體,係由以4一曱基一卜 戊烯系聚合體所構成之樹脂層、接著劑層、與4_曱基_丄一 戊烯系聚合體以外之熱可塑性樹脂所組成。然而,所使用 之4曱基-1-戊烯系聚合體以外之熱可塑性樹脂,係屬於 聚酯和聚醯胺等之含氧系熱可塑性樹脂及聚乙烯、聚丙 烯、聚1-丁烯等之烯烴系樹脂,於含氧系熱可塑性樹脂 的情況下,與專利文獻3同樣地,積層體將無法充分追隨 形成有電路之基板的凹凸,將有形成有電路之基板 膜之間的接著劑流出至Fpc電路面上的問題。另一方面, 於烯烴系聚合體樹脂的情況下,與專利文獻2同樣 =作為離型膜的情況下’烯㈣聚合體會從積層體端部超 出而附著至FPC或用於加壓的熱板上,而仍有Fpc 率降低和作業效率降低的問題。 、°σ產 專利文獻丨.曰本專利特開平2-175247號公報 專利文獻2.日本專利特開平4_28664〇號公報 專利文獻3 :日本專利特開2000-218752號公報 專利文獻4 :日本專利特開2000-263724號公報 312XP/發發明說明書(補件)/95-09/95116834 8 1294351 文獻5 ·日本專利特開2002 一179863號公報 【發明内容】 张 (發明所欲解決之問題) 本發明係提供經由熱硬化型接著劑,在將形忐古e 基板、覆蓋層臈及離型膜十”!在料成有電路之 FPC製造中,形成離型= 中進行加熱及加壓之 層的樹脂的赶出钰,义好,屬於離型膜中間層之緩衝 …且藉由追隨形成有電路之基板表面 膜之間的接著劑超出有電路之基板與覆蓋層 層體所構成之離型膜衝性的積層體、由該積 膜。 、撓性印刷電路基板製造用離型 (解決問題之手段) =明=等人為解決上述問題而潛心研究,結果發現, 猎由至乂 §有具4_甲基 特定接著層(B)及含特定射二 體之表面層(A)、 (C),if料樹脂及軟質樹脂之緩衝層 的=:)與緩衝層(c)之間具有特定接著層 ^的積層H,將可解決上述問題,遂完成本發明。 亦即’本發明係如下述。 少含有表面層⑴、接著層⑻及緩 =:Γ:ΓΑ)與緩衝層(c)之間具有接著層 曱A i 層⑴含有80〜100質量❶之4- "戊烯承5體,且該緩衝層(C)含有熔點i9(rc以 上之耐熱性樹腊(c])及炫 τ ”、、 ⑵如上述⑴記載之積層趙T二軟質樹脂⑽。 檟層體其,,接著層⑻係含有 312XP/發發明說明書(補件…孓㈣州脱料 9 1294351 20〜50質量%之4-1丄、,χ / 之4 ^基―1—戍烯系聚合體(bl)及50〜80質量 二t t原子數。2〜4之烯烴的聚合體⑽,且以荷重 g '皿度230 C所測定之熔融流動速率丨;)未、、茜 。.㈣。分鐘’.緩衝層(c)係含… 70游,丄ί )及5〇〜9〇質量%之溶點 H70C的軟質樹脂(c2)’且以荷重2為、溫度 C所測定之溶融流動速率⑽。為G 4〜iGg/iG分鐘。 質敝乙烯· 丁烯共聚合體α2_υ:二:(二)、::〇 丁烯系聚合體(b2-2)。 貝里/。之1〜 [4] 如上述[1H3]記載之積層體,其中, 熱性樹脂⑻係選自4_甲基+戊稀系聚 脂之至”種’軟質樹脂⑽係選自低密 狀低密度聚乙烯、高密度聚乙烯、丙烯之 部直鏈 丙烯共聚合體、乙烯•丙烯•丁烯共聚合體、π乙烯· 合體、乙烯·丁烯共聚合體、丙烯·丁烯共聚合體 之順丁烯二酸酐改質聚合體之至少一種。 版及具等 [5] 如上述[1]〜[4]記載之積層體,其中, 有4-曱基-1-戊烯之均聚合體、或4一甲基4 9 (Α)係含 基-1-戊烯以外之碳原子數2〜20之烯烴的共聚^稀與4~曱 [6] 如上述[1]〜[5]記載之積層體,其中,積層K〇體。 最外層為表面層(Α),該表面層(Α)的厚声氣二體之至少— 度的5〜50%。 -為知層體整體厚 312ΧΡ/發發明說明書(補件)/95_〇9/95116834 1〇 1294351 =]如上述[1]〜[6]記載之積層體,其中,加熱及加壓處理 前之積層體之表面層(A)與緩衝層(c)之間以JIS K6854為 基準測定所得的接著強度為^⑽/^丽。 [8] 如上述[1]〜[7]記載之積層體,其中,積層體之至少一 最外層為表面層(Α),該表面層(人)的面粗度Ry為〇 〇卜2〇 // m 〇 [9] 如上述[1]〜[8]記載之積層體,其中,各層係 出法而成形。 [10] —種離型臈及可撓性印刷電路基板製造用離型膜,係 由上述[1]〜[9]中任一項之積層體所構成。 (發明效果)In general, the FPC 312ΧΡ/Flip instructions (supplement)/95-09/95116834 7 1294351 are significantly less productive. In addition, although the blow molding method is proposed as the manufacturing method, it is necessary to change the size of the round mold and the swell ratio by the width of the release film, and it is difficult to make the thickness of each layer uniform, so when manufacturing the FPC =When heat and pressure, wrinkles will occur on the surface of the release film. In the case of wrinkles, the blade release film will not be able to fully follow the irregularities of the surface of the substrate on which the circuit is formed, resulting in empty yang: or wrinkle transfer. i FPC ±, so there is no way to get an FPC with a fully compliant appearance. Further, Patent Document 5 discloses a laminate in which a resin layer composed of a 4-mercapto-p-pentene polymer, an adhesive layer, and a 4-mercapto-p-pentene polymer are used. It consists of a thermoplastic resin. However, the thermoplastic resin other than the 4-mercapto-1-pentene polymer used is an oxygen-containing thermoplastic resin such as polyester or polyamide, and polyethylene, polypropylene, and polybutene. In the case of the olefin-based resin, in the case of the oxygen-containing thermoplastic resin, as in Patent Document 3, the laminate does not sufficiently follow the unevenness of the substrate on which the circuit is formed, and the substrate between the substrates is formed. The problem of the agent flowing out to the Fpc circuit surface. On the other hand, in the case of an olefin-based polymer resin, as in the case of Patent Document 2, in the case of a release film, the 'ene (tetra) polymer is attached to the FPC or the hot plate for pressurization from the end of the laminate. On, there is still a problem of lower Fpc rate and lower work efficiency. Japanese Patent Laid-Open Publication No. Hei. No. Hei. No. Hei. No. Hei. No. Hei. No. Hei. No. Hei. Japanese Patent Publication No. 2000-263724, No. 2000-263724/Inventor's Specification (Supplement)/95-09/95116834 8 1294351 Document 5 · Japanese Patent Laid-Open Publication No. 2002-179863 (Summary of the Invention) Zhang (Problem to be Solved by the Invention) The present invention Providing a layer which is heated and pressurized in a release type by using a thermosetting type adhesive, in a process of forming an EPC substrate, a cover layer, and a release film. The escaping of the resin, which is a buffer of the intermediate layer of the release film, and the release film formed by the substrate and the cover layer of the circuit layer by following the adhesive between the surface film of the substrate on which the circuit is formed The laminated body of the punctuality, the release film for the manufacture of the flexible printed circuit board (the means of solving the problem) = Ming = et al., and the research on the above problems, and found that the hunting 乂 有 § has 4 _methyl specific followed by (B) and a layer H having a specific adhesive layer between the surface layer (A), (C), the buffer layer of the specific resin and the soft resin, and the buffer layer (c), The present invention can be solved by the above problems. That is, the present invention is as follows. The surface layer (1), the subsequent layer (8), and the buffer layer (c) are provided with an adhesive layer A. The i layer (1) contains a 4- to pentene 5-body having a mass of 80 to 100 Å, and the buffer layer (C) contains a melting point i9 (heat resistant tree wax (c) above rc) and a turmeric τ", (2) The laminated layer of the T-soft resin (10) described in the above (1). The layer of the layer (8) contains the 312XP/inventive specification (supplement... 孓(4) state stripping 9 1294351 20 to 50% by mass of 4-1丄, , χ / 4 基 1 - terpene polymer (bl) and 50 to 80 mass two tt atom number. 2 to 4 olefin polymer (10), and measured by load g 'span 230 C Melt flow rate 丨;) not, 茜.. (4) minutes '. buffer layer (c) contains ... 70 swim, 丄ί ) and 5 〇 ~ 9 〇 mass % of the melting point H70C soft resin (c2) ' And with a load of 2, temperature C The melt flow rate set ⑽. For G 4~iGg/iG minutes. The ruthenium ethylene/butene copolymer α2_υ: two: (b), :: 丁烯 butene polymer (b2-2). Berry/. [1] The laminate according to the above [1H3], wherein the thermal resin (8) is selected from the group consisting of 4-methyl + pentane polyester to "species" soft resin (10) selected from low density and low density. Polyethylene, high density polyethylene, propylene partial linear propylene copolymer, ethylene propylene/butene copolymer, π ethylene · complex, ethylene · butylene copolymer, propylene / butene copolymer maleic anhydride The laminate of the above-mentioned [1] to [4], wherein the laminate has a 4-mercapto-1-pentene homopolymer or a 4-layer The copolymer of the olefin having a carbon number of 2 to 20 other than the group -1-pentene and the olefin of 2 to 20, and the layered body described in the above [1] to [5], wherein , the outer layer is the surface layer (Α), the surface layer (Α) of the thick sound of the two bodies is at least 5 to 50% - the thickness of the layer is 312 ΧΡ / hair invention instructions ( (Replacement) /95_〇9/95116834 1〇1294351 =] The laminate according to the above [1] to [6], wherein the surface layer (A) and the buffer layer of the laminate before heat and pressure treatment ( c) between JIS K68 The laminate according to the above [1] to [7], wherein at least one outermost layer of the laminate is a surface layer (Α), the surface The surface roughness Ry of the layer (human) is 2 〇 / / m 〇 [9] The laminate according to the above [1] to [8], wherein each layer is formed by a method. [10] The release film of the release type and the flexible printed circuit board is composed of the laminate of any one of the above [1] to [9].

明之積層體藉由在表面層(A)含有4一甲基— I —戊烯 系聚合體,而耐熱性與離型性優越。另外,緩衝層(C)於 製造:PC時之加熱及加壓時’因為具有優良的柔軟性,故 可追隨形成有電路之基板表面的形狀而良好變形,可防止 =有电路之基板面與覆蓋層之間之接著劑的流出。又, 2=ΐ層⑻以及具有耐熱性樹脂(cl)與軟質樹脂 ⑽之特疋組成的緩衝層(c),係加熱及加壓時的超出 :用=生因緩衝層(c)附著至形成有電路之基板面或 =及加壓之金屬板所造成之FPC製品產率降低 膜〃 +低相題,可適合使用作為FPC製造用離型 彻5116834 n 1294351 佳’工業價值極高。 【實施方式】 以下詳細說明本發明。 本發明為一種積層體,係至少含有表面層a)、 、'⑻及缓衝層⑹,而於該表面層(A)與緩衝層⑹之間且^ 接著層(B)者’其特徵為,該表面層(A)含有〜⑽質旦% ,4-甲基小戊稀系聚合體,且該緩衝層(c)含有炫點二 之耐熱性樹脂⑻及熔點17Gt:以下之軟質樹脂 亦即,本發明之積層體係基本上具有從表面侧起依序積 層由4甲基-1-戊烯系聚合體所構成的表面層(△)、接著 層(B)、緩衝層(C)並一體化之至少3層的構造。例如,從 表面側起依序積層由4_甲基―丨―戊烯系聚合體所構成的表 面層(A)、接著層(B)及緩衝層(c)、接著層(B)、由4一甲 基1-戊烯系聚合體所構成的表面層(A)並一體化之5芦 構造的積層體,可適合使用作為離型膜,尤其是Fpc制、1 籲用離型膜。 抛 ' [表面層(A)] ^ 本發明之表面層(A)只要含有80〜100質量%之4-曱基 ' ―卜戊烯系聚合體即可,除了 4-曱基-1-戊烯系聚合體二 外亦可έ有來四氟乙細等之氟系樹脂、聚苯硫、聚醋等。 本發明之表面層(Α)所使用的4-曱基-1 —戊烯系聚合 體,4-曱基-1-戊烯之均聚合體、或4一曱基一卜戊烯與^ 曱基-1-戊烯以外之碳原子數2〜20之烯烴或鏈狀二稀的 312ΧΡ/發發明說明書(補件)/95-09/95116834 12 1294351 共:合體因剛性及彈性模數良好,故較 :匕之稀煙’可舉例如乙婦、丙婦、!作為碳原:數 十八:等1烯、1~十二稀、卜十四稀、二十L:'、 佳。特別是卜癸稀因剛性及彈性模數良;故: 另外,作為此種4一甲基一 1 —、 取 有來自4-甲基-卜戊烯之構成單位’最好為以含 二=之碳原子數2,的烯經有二? 0<1.1〇 °;^ 1〜5質暑m社 貝里% 特佳為 为⑽貝里%以上之來自4 —帀 可使表面層(Α)的彈性模數增高,故較佳。之構成早位,則 、止又射此種4-甲基+戊烯系聚合體可依公知方法予以譽 :,二聚合觸媒和聚合方法並無特別限 齊格勒型觸媒(根據含有載持或非載持齒素二: ς ΐ化合物之組合者)、菲利浦型觸媒(根據載持氧化 :者)、卡明斯基(Kaminsky)型觸媒(根據載持或非載持二 茂金屬型化合物與有機銘化合物,特別是與紹四氣喃 (alUm〇Xane)之組合者)等。聚合方法有如於此等觸媒存在 下之聚體聚合法、氣相流動床聚合法、溶液聚合法,或於 壓力20MPa以上、聚合溫度1〇吖以上之高壓整體(祕) 聚合法專公知聚合方法。 具體而言,在如日本專利特開昭61 —1136〇4號公報、特 312XP/發發明說明書(補件)/95-09/95116834 13 1294351 開2003-1 05022號公報所記載般之觸媒的存在下,藉由使 4-曱基-1-戊烯單獨、或4一甲基一丨一戊烯與其以外之碳原 子數2〜20的烯烴進行共聚合,則可得到4_曱基-丨—戊烯 系聚合體。 此種4-甲基-1-戊烯系聚合體以aSTM D1238為基準, 依荷重5.0kg、溫度26(TC的條件所測定之熔融流動速率 (MFR )之值,最好為〇· 5〜2〇〇g/1〇分鐘、較佳為 分鐘、更佳為10〜l〇〇g/1〇分鐘之範圍内。若MFR2為 〇.5g/l〇分鐘〜2〇〇g/l〇分鐘之範圍内,則可得到良好的成 形性與充足的機械強度。 尚且,MFR2之值、亦即聚合體的分子量,係可 時供給至聚合系統内之氫量或聚合溫度等之設定等公知 方法而予以控制。 另=,4-甲基-1-戊烯系聚合體中,在不損及本發明目 的之範圍内,可配合耐熱定安劑、耐候安定劑、防銹劑、 耐銅害安定劑、抗靜電劑等之配合於聚烯烴中之其本身公 知的各種添加劑。 ^ “ 又,上述4-曱基-1-戊烯系聚合體最好依表面層(a)之 80〜100質量%、較佳為9〇〜1〇〇質量%、更佳為ι〇〇質量% 之比例含有。 、 [接著層B] 本發明之接著層(B)係含有20〜50質量%之4—曱基—丨一戊 烯系聚合體(bl)、及50〜80質量%之含有碳原子數&2〜4烯 烴的聚合體(b2)的樹脂組成物,較佳為含有3〇〜5〇質量% 14 312XP/發發明說明書(補件)/95-09/95116834The laminate of the present invention is excellent in heat resistance and release property by containing a 4-methyl-I-pentene polymer in the surface layer (A). In addition, the buffer layer (C) has excellent flexibility when it is heated and pressurized in the production of PC. Therefore, it can be deformed well in accordance with the shape of the surface of the substrate on which the circuit is formed, and can prevent the substrate surface of the circuit from being replaced. The outflow of the adhesive between the cover layers. Further, the 2 = enamel layer (8) and the buffer layer (c) having the composition of the heat-resistant resin (cl) and the soft resin (10) are excessively heated and pressurized: adhered to the buffer layer (c) The yield of FPC products caused by the surface of the substrate on which the circuit is formed or = and the pressure of the metal plate is reduced. The film 〃 + low phase problem can be suitably used as the FPC for the production of the type 5116834 n 1294351. [Embodiment] Hereinafter, the present invention will be described in detail. The present invention is a laminate comprising at least a surface layer a), '(8) and a buffer layer (6), and between the surface layer (A) and the buffer layer (6) and then the layer (B) is characterized by The surface layer (A) contains ~(10) proton%, a 4-methyl pentaerythrine polymer, and the buffer layer (c) contains a heat-resistant resin (8) and a melting point of 17 Gt: the following soft resin That is, the layered system of the present invention basically has a surface layer (?), an adhesive layer (B), and a buffer layer (C) which are sequentially formed of a 4 methyl-1-pentene polymer from the surface side. At least three layers of construction. For example, the surface layer (A), the subsequent layer (B), the buffer layer (c), and the subsequent layer (B) composed of a 4-methyl-nonane-pentene polymer are sequentially laminated from the surface side. The laminate of the surface layer (A) of the monomethyl 1-pentene polymer and the integrated structure of the 5 reed structure can be suitably used as a release film, in particular, a FPC system and a release liner film. Throwing '[Surface layer (A)] ^ The surface layer (A) of the present invention may contain, as long as it contains 80 to 100% by mass of a 4-fluorenyl-p-pentene-based polymer, except for 4-mercapto-1-lan The olefinic polymer may be a fluorine-based resin such as tetrafluoroethylene or the like, polyphenylene sulfide or polyester vinegar. a 4-mercapto-1 -pentene-based polymer used in the surface layer of the present invention, a homopolymer of 4-mercapto-1-pentene, or a 4-mercapto-p-pentene and a ruthenium Illustrator of the olefin or chain dimer having 2 to 20 carbon atoms other than keto-pentene/inventive specification (supplement)/95-09/95116834 12 1294351 total: the composite has good rigidity and elastic modulus, Therefore, compared with: the thin smoke of 匕 can be cited, for example, women, women, and women! As a carbon source: number eighteen: 1 ene, 1 ~ twelve rare, fourteen thin, twenty L: ', good. In particular, the diorite has a low rigidity and a good elastic modulus; therefore: In addition, as such a 4-methyl- 1 -, a constituent unit derived from 4-methyl-p-pentene is preferred to contain two = The number of carbon atoms is 2, and the olefins have two 0<1.1 〇; ^ 1~5 质 m 社 % % % % 特 ( ( ( ( ( 10 10 10 10 10 10 10 10 10 10 10 10 10 10 10 10 10 10 10 10 10 10 10 10 10 The modulus of elasticity is increased, so it is preferred. In the early position, the 4-methyl+pentene polymer can be known by known methods: the two polymerization catalysts and the polymerization method are not particularly limited to Ziegler type catalysts (according to Carrier or unsupported dentate II: 组合 ΐ compound combination), Phillips type catalyst (according to carrier oxidation:), Kaminsky type catalyst (based on carrier or unloaded) Holding a metallocene type compound and an organic compound, especially a combination with a sulphonic acid (alUm〇Xane) and the like. The polymerization method is a polymer polymerization method, a gas phase fluidized bed polymerization method, a solution polymerization method in the presence of such a catalyst, or a high pressure overall (secret) polymerization method having a pressure of 20 MPa or more and a polymerization temperature of 1 Torr or more. method. Specifically, the catalyst is as described in Japanese Patent Laid-Open Publication No. SHO 611-1136-4, No. 312XP/Inventive Specification (Supplement), 95-09/95116834, 13 1294351, and No. 2003-1 05022. In the presence of 4-mercapto-1-pentene alone or 4-methyl-monopentene and other olefins having 2 to 20 carbon atoms, a 4-mercapto group can be obtained. - a quinone-based polymer. The 4-methyl-1-pentene polymer is based on aSTM D1238 and has a value of a melt flow rate (MFR) of 5.0 kg and a temperature of 26 (TC conditions, preferably 〇·5~). 2 〇〇 g / 1 〇 minutes, preferably minutes, more preferably 10 ~ l 〇〇 g / 1 〇 minutes. If MFR2 is 〇. 5g / l 〇 minutes ~ 2 〇〇 g / l 〇 minutes In the range of the above, a good moldability and a sufficient mechanical strength can be obtained. The value of MFR2, that is, the molecular weight of the polymer, is a known method such as setting of the amount of hydrogen or the polymerization temperature which can be supplied to the polymerization system. Further, the 4-methyl-1-pentene polymer can be blended with a heat-resistant stabilizer, a weather-resistant stabilizer, a rust preventive, and a copper-resistant stabilizer without damaging the object of the present invention. a compound, an antistatic agent, or the like, which is blended with various additives known per se in the polyolefin. ^ " Further, the above 4-mercapto-1-pentene polymer is preferably 80 to 100 by mass of the surface layer (a). %, preferably 9〇~1〇〇% by mass, more preferably ι〇〇% by mass. [, Next layer B] The adhesive layer (B) of the present invention Resin composition having 20 to 50% by mass of a 4-mercapto-quinone pentene polymer (bl) and 50 to 80% by mass of a polymer (b2) having a carbon number & 2 to 4 olefin Preferably, it contains 3〇~5〇% by mass. 14 312XP/Inventive Manual (supplement)/95-09/95116834

1294351 之4-曱基-卜戊烯系聚合體(bl)、及5〇〜7〇質量%之含有 碳原子數2〜4烯烴系聚合體(b2)的樹脂組成物。 。另外,以ASTMD1238為基準,依荷重2l6kg、溫度23〇 C所測定之接著層(B)的熔融流動速率(MFRl)的值為未滿 0· 4g/l〇刀|里,較佳為〇· 〇1〜〇· 3g/i〇分鐘、更佳為 〇·〇5〜0.3g/10分鐘。較接近於Fpc製造時加熱及加壓 作時之溫度的溫度230°C下之MFR1的值,若為上述範圍 内,則於FPC製造時之加壓及加熱時,將可減少緩衝層(C) 的超出。 又,藉由使用此種特定的接著層^),含有與其他樹脂 之接著性一般而言較弱之4-曱基+戊稀系聚合體的表面 層(A),將可得到充分之與緩衝層(c)的接著強度。 再者,本發明之接著層(趵中,最好含有4_曱基—卜戊 烯系聚合體(bl) 20〜50質量❶/。、作為碳原子數2〜4的烯烴 系聚合體(b2)之乙烯•丁烯共聚合體(btDpw質量%^ 1-丁烯系聚合體(b2-2)30〜60質量%的樹脂組成物',更°佳 為含有4-甲基-1-戊烯系聚合體(bl)3〇〜5〇質量%、乙烯· • 丁烯共聚合體(b2_l)10〜30質量%、及卜丁烯系聚合體 、(b2-2)40〜60質量%之樹脂組成物。 〜 又,在不損及本發明特性的範圍内,亦可含有上述 、(bl)、(b2-1)及(b2-2)以外的其他熱可塑性樹脂,而於接 著層(B)中,相對於其他熱可塑性樹脂、(bl)、(b2〇及 (b2-2)的合計量,(bl)、(b2-1)及(b2-2)的合計量為 80〜100質量%、更佳為90〜1〇〇質量%。 °里…、 312XP/發發明說明書(補件)/95-09/95116834 15 1294351 銅::二:可含有耐熱定安劑、耐候安定劑、防銹劑、耐 劑、抗靜電劑等之配合於聚烯烴中之其 n添加劑’此物脂及安定劑等之添加劑的混合方 .法。α +例如乾式摻合或利用擠出機之炼融摻合等公知方 之二:層經由接著層⑻積層所得 之門^蛀〇 〇、、及加壓處理前之表面層(Α)與緩衝層(c) 二 度’可例如依下述方法進行測定:從使用3 層⑹^接^拉具裝置所得之由表面層(A)/接著層⑻/緩衝 層⑻/表面層⑴之5層所構成的積層體,切 = ^50随、寬度15mm之樣品’根據JIS_4,從樣 =度方向之一端面使單側的表面層⑴稍微剝離,將該 邻八八2丨+ u)㈣離之表面層(Α)以外的積層體剩餘 ::刀別以夾具夾著,以溫度23t、剝離角度⑽度、 剝離速度300_/分、剝離寬度15職的條件,進行τ字型 剝離試驗。 朴加熱及加塵處理前之表面層⑴與緩衝層(c)之間的接 者強度為卜20N/15mm、較佳為H0N/15随、更佳為 2〜咖_、特佳為4〜8N/15mm,積層體之表面層⑴盘緩 ,層(c)之間的接著強度若為上述範圍内’則於Fpc製造 時之加壓及加熱時,可減少緩衝層((:)的超出。 再者,依接近將本發明之積層體使用作為Fpc製造時之 離型膜時之加熱及加壓處理條件的例如溫度18〇。^、壓力 5MPa ’進行30分之加熱及加壓處理後,冷卻所得之加熱A 4-mercapto-p-pentene-based polymer (b1) of 1294351 and a resin composition containing 5 to 4% by mass of the olefin-based polymer (b2) having 5 to 7 % by mass. . Further, based on ASTM D1238, the value of the melt flow rate (MFR1) of the adhesive layer (B) measured at a load of 21.6 kg and a temperature of 23 〇C is less than 0.4 g/l of trowels, preferably 〇· 〇1~〇·3g/i〇 minutes, more preferably 〇·〇5~0.3g/10 minutes. The value of MFR1 at a temperature of 230 ° C which is closer to the temperature at the time of heating and pressurization at the time of Fpc production, if it is within the above range, the buffer layer can be reduced during pressurization and heating at the time of FPC production. Exceeded. Further, by using such a specific adhesive layer, the surface layer (A) of a 4-mercapto+pentane-based polymer which is generally weak in adhesion to other resins can be sufficiently obtained. The adhesion strength of the buffer layer (c). Further, in the adhesive layer of the present invention, it is preferable that the fluorene-containing polymer (b) is a olefin-based polymer having a carbon number of 2 to 4 as a carbon atom having 2 to 4 carbon atoms. B2) ethylene/butene copolymer (btDpw mass%^ 1-butene polymer (b2-2) 30 to 60% by mass of resin composition', more preferably contains 4-methyl-1-pentyl The olefin polymer (bl) is 3 〇 to 5 〇% by mass, the ethylene·• butene copolymer (b2_1) is 10 to 30% by mass, and the butene-based polymer (b2-2) is 40 to 60% by mass. Resin composition. Further, other thermoplastic resins other than the above, (bl), (b2-1), and (b2-2) may be contained in the range of the present invention without impairing the characteristics of the present invention. In B), the total amount of (bl), (b2-1), and (b2-2) is 80 to 100 with respect to the total amount of other thermoplastic resins, (bl), (b2〇, and (b2-2). % by mass, more preferably 90~1〇〇% by mass. °里..., 312XP/Inventive Manual (supplement)/95-09/95116834 15 1294351 Copper:: 2: It can contain heat-resistant stabilizer, weathering stabilizer, Rust inhibitor, anti-agent, antistatic agent, etc. Mixing method of the additive of the n-additive 'the grease and the stabilizer, etc. in the polyolefin. α + such as dry blending or refining blending using an extruder, etc. The layer (8) obtained by laminating the layer (8) and the surface layer (Α) and the buffer layer (c) before the pressure treatment can be measured, for example, by the following method: from the use of 3 layers (6) ^ A laminate consisting of five layers of the surface layer (A) / the subsequent layer (8) / the buffer layer (8) / the surface layer (1) obtained by the pulling device, and the sample of the cut width = ^50 with a width of 15 mm 'according to JIS_4, sample = degree One end of the direction causes the surface layer (1) on one side to be slightly peeled off, and the adjacent layer of the surface layer (Α) of the neighboring 八八丨2 u) (4) is left: the knife is sandwiched by the jig at a temperature of 23t, The peeling angle (10) degree, the peeling speed of 300_/min, and the peeling width of the 15th position were subjected to the τ-type peeling test. The strength between the surface layer (1) and the buffer layer (c) before the heating and dusting treatment was 20N/15mm, preferably H0N/15, more preferably 2~coffee_, especially good 4~8N/15mm, surface layer of laminated body (1) When the bonding strength between the layers (c) is within the above range, the buffer layer ((:) is excessively reduced during pressurization and heating at the time of Fpc production. Further, the laminate of the present invention is used close to The heating and pressurization treatment conditions in the case of the release film at the time of Fpc production are, for example, a temperature of 18 〇, and a pressure of 5 MPa. After heating and pressurizing for 30 minutes, the heating is performed by cooling.

312XP/發發明說明書(補件)/95-09/95116834 16 1294351 及加壓處理後的積層體中,表面層(A)與緩衝層(c)之間根 據Jis K6854測定所得之接著強度最好為卜1〇N/i5mm、 較佳為1〜5N/15_、更佳為2~4Ν/15_。 #加熱f加壓處理後之表面層(Α)與緩衝層(C)之間的接 著舍X若為上述範圍内,則於利用加熱及加屋處理之覆芸 層之接著處理後,從覆蓋層剝離離型臈時,將可防止離^ 膜破裂等覆蓋層殘留於表面的情況。 (4 -甲基-1-戊烯系聚合體(bl)) 二發層⑻所使用之4_甲基+戍稀系 體:目)同:使用與用於表面層⑴之一戍稀系聚合 (含碳原子數2〜4之烯烴的聚合體(b2)) =發明之接著層⑻所使用之 聚合體(b2),若為人妙広7 a 双& 4 <琊烴的 亦可為該婦經之均;二體即可, 數2〜4之烯烴的聚合體(b2 ς = 聚合體(b2A及卜丁稀系聚合體⑽丁稀共 (乙烯•丁烯共聚合體(b2-l)) 本發明之接著> (㈣,最好為卜‘斤使曰用之乙烯·丁烯共聚合體 質量%之無規共聚::3二質量㈣為15, =可r.t1,'異丁…烯ί其、中:二 烯Α 丁烯為較佳。此等丁烯可罝想# ’、 2種以上使用。 早獨使用1種,或組合 312卿翻說明書(補件細/95116834 17 1294351 乙烯•丁烯共聚合體“卜〗)的上述組成 为夕卜 13c-nmr而測定。又,乙嫌•丁、p # 、、、成,力措田312XP/Inventive Manual (Supplement)/95-09/95116834 16 1294351 and the pressure-treated laminate, the surface layer (A) and the buffer layer (c) have the best adhesion strength according to Jis K6854. It is 1/N5 mm, preferably 1 to 5 N/15_, more preferably 2 to 4 Å/15_. #热热 The pressure between the surface layer (Α) and the buffer layer (C) is within the above range, after the subsequent treatment with the coating layer by heating and room cleaning, the coating is covered. When the layer is peeled off, it is possible to prevent the coating layer from being left on the surface such as cracking of the film. (4-methyl-1-pentene polymer (bl)) 4-methyl+anthracene used in the second layer (8): the same as: used and used in the surface layer (1) Polymerization (polymer (b2) containing an olefin having 2 to 4 carbon atoms) = polymer (b2) used in the subsequent layer (8) of the invention, if it is a sulfonium 7 a double & 4 < It can be the average of the women; the two-body can be a polymer of 2 to 4 olefins (b2 ς = polymer (b2A and butadiene polymer (10) butadiene (ethylene/butene copolymer (b2) -l)) Following the present invention> ((4), preferably, random copolymerization of ethylene-butene copolymer mass% by weight: 3 mass (four) is 15, = r.t1, 'Isobutyl...Alkene, Middle:Diene oxime Butene is preferred. These butenes can be used as '#, two or more. Use one type alone, or a combination of 312 clear instructions (small parts) /95116834 17 1294351 The above composition of the ethylene/butene copolymer "Bu" is measured by the 13c-nmr. In addition, B. Ding, p #, ,, 成,力措田

π1〇,, 朴去 烯丁烯/、聚合體(b2-l)根據ASTM 車 r、更二二:Η’10分鐘、較佳為1,/10分 知更佳為卜1〇g/10分鐘。此種乙稀•丁稀共聚 依么知方法使各單元體聚合而獲得,卿)之值、亦即p 體:分子量,係可藉由聚合時供給至聚 : 聚合溫度等之設定等公知方法而予以控制。又,亦 ^輕易取得,可舉例如三井化學(股)製之商 Α妨㈧」、住友化學(股)製之商品名「ΕβΜ」等。 稀 脂 述1-丁稀系聚合體(b2—2)的混合性變好,;=二: 表面層(A)及緩衝層⑹具有高接著性能㈣^對於 (1-丁烯系聚合體(b2_2)) 者θ (B)。 之接著層⑻所使用之卜丁烯系聚合體(叫 Γ之1’、丁 八有! 6〇,°質量%、較佳為δο,〇質量 成的共聚合體一或卜丁烯與卜丁婦以外之婦烴所構 2卜丁稀共聚合所用m稀以外之 乙浠::稀、卜己稀、卜辛稀、卜癸烯、卜十::例如 十八烯等之碳原子數2、3及5〜20之烯烴等。其 :=較佳。此等烯煙可單獨使用1種,;可組:乙2 312XP/發發明說明書贿牛)/95·〇9/95 i}咖4 18 1294351 i:了:线合體则的上述組成’可藉由,_而 ,: 了烯系聚合體(b2~2)根據ASTM D1238,以 -二:!Γ溫度以吖所測定之熔融流動速率⑽。的 值為0.卜5Gg/1()分鐘、較佳為分鐘、更佳為 .广2g/l〇分鐘。此種卜丁稀系聚合體可依公知方法使久 早几體聚合而獲得,猶】之值、亦即聚合體的 ; 給至聚合系統内之氯量或聚合溫度等: =專公知方法而予以控制。又,亦可由市場輕易取得, 〇牛列如二井化學(股)製之商品名「TAFMER BL」等。 /藉由使用樹脂組成及MFR1之值為±述範_之、 :聚合體(:2),貝甲基+戊烯系聚合體⑽及乙 、•丁細共聚合體(b2-l)的混合性變好’而可得到對於 面層(A)及緩衝層⑹具有高接著性能的接著、、 [緩衝層(C)] 本發明之緩衝層(C)若為含有炫點19(rc以上之耐敎性 樹脂(⑴及炼點170t^下之軟質樹脂(c2)者即可,而在 不損及本發明目的之範圍内,可含有溶點超過17代 滿19(TC之熱可塑性樹脂,以及耐熱定安劑、耐候安定巧、 防銹劑、耐銅害安定劑及抗靜電劑等之配合於聚稀烴中月之 其本身公知的各種添加劑。 此等樹月旨及安定劑等之添加劑的混合方法,可舉例如 式摻合或利用擠出機之熔融摻合等公知方法。 j發明之緩衝層(c)最好依10〜50質量%、較佳為1(M5 貝里i更Y土為15〜40質量%的比例含有熔點19〇。〇以上之 312XP/發發明說明書(補件)/95-〇9/95 j】6834 19 1294351 :熱性樹脂(cl)。又,最好依50〜90質量%、較佳為55〜90 質量%、更佳為60〜85質量%的範圍含有熔點170°C以下之 軟質樹脂(c 2 )。Π1〇,, 朴烯烯/, polymer (b2-l) according to ASTM car r, more than two: Η '10 minutes, preferably 1, /10, better known as Bu 1〇g/10 minute. The ethylene-butadiene copolymerization method is obtained by polymerizing each unit body, and the value of the unit, that is, the p-body: molecular weight, is a known method such as supply to polymerization: polymerization temperature, etc. And to control. In addition, it is easy to obtain, for example, the trade name of "Mitsui Chemical Co., Ltd." (8), and the product name of "Shinjuku Chemical Co., Ltd.", "ΕβΜ". The mixing property of the 1-buty-thick polymer (b2-2) is better, and the second layer: the surface layer (A) and the buffer layer (6) have high adhesion properties (4) for (1-butene-based polymer ( B2_2)) θ (B). The butene-based polymer used in the layer (8) (called 1', 丁八有! 6〇, °% by mass, preferably δο, 〇 mass of the copolymer 1 or bubutene and pudding In addition to the diuretic co-polymerization of the diuretic co-polymerization of the woman other than the woman, the bismuth other than the m-dilute co-polymerization: dilute, di-diluted, di-n-dish, diterpene, b::, for example, octadecene, etc. , 3 and 5 to 20 olefins, etc.: = preferred. These olefins can be used alone; can be grouped: B 2 312XP / issued instructions for bribes / 95 · 〇 9 / 95 i} coffee 4 18 1294351 i: The above composition of the wire combination can be obtained by _, and: the olefin polymer (b2~2) according to ASTM D1238, the melt flow measured by -: Γ Γ temperature Rate (10). The value is 0. 5 Gg / 1 () minutes, preferably minutes, more preferably 2. 2 g / l 〇 minutes. Such a dibutyl polymer can be obtained by polymerizing a long-term body according to a known method, that is, a value of a polymer, a chlorine amount or a polymerization temperature to be supplied to a polymerization system, etc.: Control it. Moreover, it can be easily obtained by the market, and the yak is listed as the trade name "TAFMER BL" manufactured by Mitsui Chemicals Co., Ltd. / by using a resin composition and a value of MFR1 of ±, a mixture of a polymer (: 2), a betyl methyl group + a pentene polymer (10), and a mixture of a B and a butylene fine copolymer (b2-l) If the property is improved, it is possible to obtain a high adhesion property to the top layer (A) and the buffer layer (6). [Buffer layer (C)] The buffer layer (C) of the present invention contains a bright point 19 (rc or more). The sturdy resin ((1) and the soft resin (c2) under the refractory point 170t) may contain a thermoplastic resin having a melting point of more than 17 generations of 19 (TC) within a range not detracting from the object of the present invention. And additives such as heat-resistant stabilizers, weather-resistant stabilizers, rust inhibitors, copper-resistant stabilizers, and antistatic agents, etc., which are well-known in the month of polysulfide. The mixing method may, for example, be a known method such as blending by means or melt blending using an extruder. The buffer layer (c) of the invention is preferably 10 to 50% by mass, preferably 1 (M5 Berry i The ratio of Y soil is 15 to 40% by mass, and the melting point is 19 〇. The above 312XP/inventive specification (supplement)/95-〇9/95 j]6834 19 1294351: Resin (cl). Further, by preferably 50~90 mass%, preferably 55~90% by mass, more preferably in a range of 60~85% by mass having a melting point of 170 ° C or less soft resin (c 2).

另外,根據ASTM D1238,以荷重2· 16kg、溫度230°C 所測定之緩衝層(C)之熔融流動速率(MFRi)的值為 0·4〜l〇g/i〇分鐘、較佳為〇 4〜9g/1()分鐘、更佳為 0·4〜5g/l〇分鐘、再更佳為〇.5〜4g/1〇分鐘、特佳為 〇·5〜3g/l〇分鐘。 藉由使用上述依上述組成範圍含有具特定熔點範圍之 耐熱性樹脂(cl)及軟質樹脂(c2),並具有屬於上述MFRl 範圍之緩衝層(c)的積層體,作為FPC製造時的離型膜, 則可得到良好的緩衝性,並可防止接著劑超出,同時可防 止緩衝層本身的超出。 (耐熱性樹脂(cl)) 本發明之緩衝層(c)所使用之熔點為19(rc以上的耐熱 性樹脂(cl),最好為熔點19(rc以上、較佳為19〇〜25〇t:、 ^佳為200〜250°C之樹脂。若熔點為19(rc以上,則Fpc =造時之加熱及加壓時樹脂不致熔解,而可減少緩衝層的 ,出。又,右熔點為2501以下,藉由以擠出機進行熔融 此練,則可得到耐熱性樹脂(cl)與熔點17〇它以下軟質樹 脂(c2)之具有良好分散性的組成物。 另外,耐熱性樹脂(cl)根據ASTM D1238,以荷重5kg、 溫度26(TC所測定之緩衝層((:)之熔融流動速率(mfr2)的 值為0.5〜200g/l〇分鐘、較佳為卜15〇g/1〇分鐘、更佳為 312XP/發發明說明書(補件)/95-09/95116834 20 1294351 10〜100g/10 分鐘。 作為滿足上述條件的耐熱性樹脂(cl),具體可例示如使 用於上述表面層(A)之基-1-戊烯系聚合體;聚對苯 一甲酸乙二酯(PET)、聚對苯二甲酸丁二酯(ρΒΤ)等之聚 '酯;聚醯胺-6、聚醯胺-6,6、聚醯胺11、聚醯胺12等之 聚醯胺。此等樹脂可由市場輕易取得,例如三菱工程塑膠 (股)製之商品名「Novamid」、東麗(股)製之商品名 • 「Amilan」等。又,此等熔點為190t以上之樹脂可單獨 籲使用,亦可組合2種以上使用。此等之中,由得到 層:B)之良好接著強度而言,以4_甲基+戊烯系聚合體 及聚醯胺為較佳,特別是可適合使用與用於表面層⑴之 4-甲基-1-戊烯系聚合體相同者。 (軟質樹脂(c2)) 本發明之緩衝層(c)所使用之熔點為17(rc以下的軟質 樹脂(C2),最好為其熔點17(rc以下、較佳為7〇〜17代、、 _ f = 8〇〜⑽、特佳為90〜職之樹脂。此樹脂係熔 ‘讀低’於FPC製造時之加熱及加a時容易變形,將追隨 .形,有電路之基板表面的凹凸,防止形成有電路之基板與 覆蓋層膜之間的接著劑流出至Fpc的電路面上,亦即具^ •所謂緩衝機能的樹月旨。軟質樹脂(c2)的炫點若為17_ 下,、則於FPC製造時之加熱及加壓時容易變形,而可追隨 形成有電路之基板表面的凹凸,若熔點為7〇它以上, 加熱及加壓時樹脂不致大量流出,可減少緩衝層(c)之超 312XP/發發明說明書(補件)/95.09/95116834 21 ⑧ 1294351 另外,軟質樹脂(C2)根據ASTMD1238,以荷重2 16kg、 溫度230 °C所測定之熔融流動速率(MFRl)的值為 0.8〜25g/10分鐘、較佳為卜20g/10分鐘、更佳為W5g/i’〇 分鐘。 • 作為滿足上述條件之軟質樹脂(c2),具體有如低密度聚 乙烯、直鏈狀低密度聚乙烯、高密度聚乙烯、丙烯之均聚 合體、乙烯•丙烯共聚合體、乙烯•丙烯•丁烯共聚合體^ 丁稀之均聚合體、乙烯•丁烯共聚合體、丙烯•丁^共聚 δ體再者為了使之與熔點19 〇 C以上之耐熱性樹脂(c 1) 的接著性變得良好,亦可摻合將此等樹脂藉由不飽和幾酸 及/或其衍生物進行接枝改質者。除此之外,可舉例如選 自乙烯X·丙烯酸酯共聚合體、乙烯•甲基丙烯酸酯共聚合 體、乙烯•醋酸乙烯酯共聚合體、乙烯•丙烯酸共聚合體、 乙烯·甲基丙烯酸共聚合體、及由其等之部分離子交U聯物 選出之共聚合體等之樹脂。此等樹脂可由市場輕易取得, 可舉例如二井杜邦polychemicals(股)製之商品名 「EVAFLEX」、商品名「NUCREL」;住友化學(股)勢之商口 f :Eve齡」、商品名「㈣也」。另外,:等溶: 170 C以下之樹脂可單獨使用,亦可組合2種以上使用。 此等之中,由可於溫度13代附近炫融而言,較佳為低密 度聚乙烯、直鏈狀低密度聚乙烯(乙烯含有量為8〇質量% 以上之乙稀與碳原子數3〜1〇的α_烯烴之共聚合體)、丙 婦之均聚合體、丙烯•丁烯共聚合體及以项丁稀二酸 行接枝改質之聚乙烯。 312ΧΡ/發發明說明書(補件)/95-09/95116834 22 1294351 [積層體] :::月之積層體係至少含有表面層⑴、接著層⑻及緩 务曰(C)’亚於表面層(A)與緩衝層(c)之間具有接著声 =積層體,若於該積層體之至少一最外層具有表心 :二’亦可具有表面層⑴、接著層⑻及緩衝層(c)以外 =較佳可舉例如(A)/⑻/(c)之3層構造的積層體、 (V(B)/(C)/(D)之4層構造的積層體 (A)/(B)/(C)/(B)/(A)之5層構造的積層體等。此等之 中’特佳係使用作為離型膜時不需表背面區別之於兩侧最 外層具有表面層(A)之5層構造的積層體。另外,作為可 使用於4層構造之積層體的層⑼之樹脂,最好為具有高 耐熱性的熱可塑性樹脂,可例示如聚對苯二甲酸乙二酉匕 (_、聚對苯二曱酸丁二酯(pBT)等之聚酯;聚醯胺_6曰、 聚醯胺-6, 6、聚醯胺U、聚醯胺12等之聚醯胺;及聚甲 基^戊烯,·此等樹脂可由市場輕易取得,例如三菱工程塑膠 (股)製之商品名「Novamid」、東麗(股)製之商品名 二Amilan」、三井化學(股)製之商品名「τρχ」等。又,此 等樹脂可單獨使用,亦可組合2種以上使用。 /另外,本發明之積層體中,表面層(Α)、接著層(β)及緩 衝層(C)之厚度係依積層體使用用途而異,但於使用作為 即^製造用離型膜的情況下,積層體厚度為1〇〜1〇〇〇#爪、 較佳為+20〜500 /zm、更佳為3〇〜4〇〇//m、再更佳為4〇〜2〇〇 。若厚度為此範圍内,則作為捲起物使用時的處理性 良好,若為10/z m以上則可得到各層厚薄精度良好的積層 312XP/發發明說明書(補件)/95-09/95116834 23 1294351 Γηι另^^面層⑴的厚度最好為5〜副"、較佳為5〜50 1 1〇〇 土 ^ 5〜4〇#m。另外,接著層(B)的厚度最好為 〇 _、較佳為卜5Mm、更佳為14〇_。又緩衝 層(c)的厚度最好為10〜6〇〇 、、 為20〜200 “。 丨“為1〇〜300 "、更佳 再者,屬於積層體之至少—最外層的表面層⑴ 積層體整體厚度的5〜5G%、較佳為5〜45%、更佳Further, according to ASTM D1238, the value of the melt flow rate (MFRi) of the buffer layer (C) measured at a load of 2·16 kg and a temperature of 230 ° C is 0·4 〜 l 〇 g / i 〇 minutes, preferably 〇 4 to 9 g / 1 () minutes, more preferably 0 · 4 ~ 5g / l 〇 minutes, more preferably 〇. 5 ~ 4g / 1 〇 minutes, particularly good 〇 · 5 ~ 3g / l 〇 minutes. By using the above-mentioned composition range, the heat-resistant resin (cl) having a specific melting point range and the soft resin (c2) and having the buffer layer (c) belonging to the above-mentioned MFR1 range are used as the release type at the time of FPC production. The film provides good cushioning and prevents the adhesive from exceeding, while preventing the buffer layer itself from exceeding. (Heat-Resistant Resin (cl)) The heat-resistant resin (cl) having a melting point of 19 (rc or more) used in the buffer layer (c) of the present invention preferably has a melting point of 19 (rc or more, preferably 19 Å to 25 Å). t:, ^ is preferably a resin of 200 to 250 ° C. If the melting point is 19 (rc or more, Fpc = resin does not melt when heated and pressurized, but can reduce the buffer layer, and the right melting point When it is 2501 or less, it melts this by an extruder, and it can obtain the composition of the heat-resistant resin (cl) and the soft resin (c2) below the melting point of the soft resin (c2). Moreover, heat-resistant resin ( Cl) according to ASTM D1238, with a load of 5 kg and a temperature of 26 (the buffer layer ((:) melt flow rate (mfr2) measured by TC is 0.5 to 200 g/l min, preferably 15 g/l 〇 、 、 312 312 312 312 312 312 312 312 312 312 312 312 312 312 312 312 312 312 312 312 312 312 312 312 312 312 312 312 312 312 312 312 312 312 312 312 312 312 312 312 312 312 312 312 312 312 312 312 312 312 312 312 312 312 Layer 1-A pentene polymer (P), polyethylene terephthalate (PET), polybutylene terephthalate (ρΒΤ) Poly-esters; polyamines such as polyamido-6, polyamido-6,6, polydecylamine 11, polydecylamine 12, etc. These resins are readily available from the market, such as Mitsubishi Engineering Plastics Co., Ltd. The product name "Novamid", the product name of Toray (share), "Amilan", etc. These resins having a melting point of 190t or more can be used alone or in combination of two or more. From the viewpoint of the good adhesion strength of the obtained layer: B), a 4-methyl+pentene polymer and a polyamine are preferable, and in particular, 4-methyl-1 which is used for the surface layer (1) can be suitably used. - The pentene-based polymer is the same. (Soft resin (c2)) The softening resin (C2) having a melting point of 17 (rc or less) used in the buffer layer (c) of the present invention preferably has a melting point of 17 (rc or less). Preferably, it is a resin of 7〇~17, _f=8〇~(10), and a special 90~. This resin is melted 'read low' and is easily deformed when heated by FPC and will be followed by Shape, the unevenness of the surface of the substrate of the circuit prevents the adhesive between the substrate on which the circuit is formed and the film of the cover film from flowing out onto the circuit surface of the Fpc, that is, The function of the buffering function is as follows: if the soft resin (c2) has a bright point of 17_, it is easily deformed during heating and pressurization during FPC production, and can follow the unevenness of the surface of the substrate on which the circuit is formed. 7 〇 above, the resin does not flow out a lot when heated and pressurized, can reduce the buffer layer (c) super 312XP / invention manual (supplement) / 95.09/95116834 21 8 1294351 In addition, the soft resin (C2) according to ASTM D1238, The value of the melt flow rate (MFR1) measured at a load of 2 16 kg and a temperature of 230 ° C is 0.8 to 25 g/10 min, preferably 20 g/10 min, more preferably W 5 g/i' min. • As the soft resin (c2) satisfying the above conditions, specifically, low density polyethylene, linear low density polyethylene, high density polyethylene, propylene homopolymer, ethylene propylene copolymer, ethylene propylene/butene In order to make the adhesion to the heat-resistant resin (c 1) having a melting point of 19 〇C or more, the copolymerization of the homopolymer, the ethylene/butene copolymer, and the propylene/butylene copolymer are further improved. It is also possible to blend these resins by graft modification with unsaturated acids and/or derivatives thereof. In addition, examples thereof include an ethylene X·acrylate copolymer, an ethylene/methacrylate copolymer, an ethylene/vinyl acetate copolymer, an ethylene/acrylic acid copolymer, an ethylene/methacrylic acid copolymer, and A resin such as a copolymer or the like selected from a part of the ion-exchanged U-linked product. Such resins are readily available from the market, such as the trade name "EVAFLEX" manufactured by Mitsui DuPont Polychemicals Co., Ltd., and the trade name "NUCREL"; the commercial reputation of Sumitomo Chemical Co., Ltd. f: Eve Age, and the product name (4) and also". In addition, the resin may be used alone or in combination of two or more kinds. Among these, it is preferably low-density polyethylene or linear low-density polyethylene (ethylene content of 8% by mass or more of ethylene and carbon atoms 3). a copolymer of ~1 α of α-olefins, a homopolymer of propylene, a propylene/butene copolymer, and a polyethylene modified by grafting with a disaccharide. 312ΧΡ/发发明说明(补件)/95-09/95116834 22 1294351 [Laminated body] ::: The monthly laminated system contains at least the surface layer (1), the subsequent layer (8) and the buffer layer (C)' subsurface layer ( A) having a contiguous sound = laminated body between the buffer layer (c) and having a centroid at least one outermost layer of the laminated body: the second layer may have a surface layer (1), an adhesive layer (8), and a buffer layer (c) Preferably, for example, a laminated body having a three-layer structure of (A)/(8)/(c) and a laminated body (A)/(B) having a four-layer structure of (V(B)/(C)/(D) /(C)/(B)/(A) A layered structure of a 5-layer structure, etc. Among these, the "extraordinary system" is used as a release film, and the outermost layer on both sides has a surface layer ( A) a layered structure having a five-layer structure. Further, as the resin of the layer (9) which can be used for the laminate of the four-layer structure, a thermoplastic resin having high heat resistance is preferable, and for example, polyethylene terephthalate is exemplified.酉匕 (_, polybutylene terephthalate (pBT) and other polyester; polyamine -6 曰, polyamine-6, 6, polyamine U, polyamide 12, etc. Amine; and polymethyl pentene, these resins can be easily obtained from the market, for example The product name "Novamid" manufactured by Mitsubishi Engineering Plastics Co., Ltd., the product name "Amilan" manufactured by Toray Industries Co., Ltd., and the product name "τρχ" manufactured by Mitsui Chemicals Co., Ltd., etc. These resins can be used alone. In addition, in the laminated body of the present invention, the thicknesses of the surface layer (Α), the adhesive layer (β), and the buffer layer (C) vary depending on the use of the laminate, but are used as That is, in the case of manufacturing a release film, the thickness of the laminate is 1 〇 1 〇〇〇 # claw, preferably +20 to 500 / zm, more preferably 3 〇 to 4 〇〇 / / m, and even more When the thickness is within this range, the handleability when used as a rolled material is good, and if it is 10/zm or more, a laminate 312XP having a good thickness and thickness can be obtained. Piece) /95-09/95116834 23 1294351 Γηι又^^ The thickness of the surface layer (1) is preferably 5~sub ", preferably 5~50 1 1 ^^^ 5~4〇#m. In addition, The thickness of the layer (B) is preferably 〇_, preferably 5Mm, more preferably 14〇. The thickness of the buffer layer (c) is preferably 10~6〇〇, 20~200" | 'Or better ", as 1〇~300 Further, at least part of the laminate - 5~5G% of the overall thickness of the outermost surface layer ⑴ laminate, preferably 5~45%, more preferably

‘、:3〇%、再更佳為5〜25%,特佳為10〜25%,則FPC梦造 :之加熱及加壓時,緩衝層(〇的超出量少,且對於形‘ 有電路之基板表面的凹凸之追隨性良好,可防止形成 路之基板與覆蓋層膜之間之接著劑流出。',: 3〇%, more preferably 5~25%, especially preferably 10~25%, then FPC dreams: when heating and pressurizing, the buffer layer (the amount of 〇 is less, and for the shape ' The follow-up of the unevenness on the surface of the substrate of the circuit is good, and the flow of the adhesive between the substrate forming the path and the cover film can be prevented.

另外’屬於積層體之至少一最外層的表面層⑴,根據 JIS B_1所測定之面粗度Ry丨u卜2G"、較佳為 〇.1〜=//111、更佳為0.1〜5//111。表面層(幻之面粗度若為 上述範圍内,則FPC製造時之加熱及加壓後剝離離型膜時 的離型性良好。製造此種面粗度之積層體的方法並無特別 限制,可藉由公知方法予以製造,於使用τ—模具裝置之 擠出成形法中,藉由使用將冷輥、亦即冷卻輥的表面以消 光處理變_者,將冷輕之表面轉印至⑽融之樹脂上 後,予以冷卻,則可輕易得到上述範圍的粗度。另外,於 製造表面平滑之積層體後,再度將該積層體加熱而軟化, 同時以壓花輥進行加熱及加壓處理,使積層體表面呈均勻 粗糙,則可得到目的之面粗度。 另外,本發明之積層體的製造方法並無特別限制,可藉 312XP/發發明說明書(補件)/95·〇9/95116834 24 1294351 2用丁-模具裝置的擠出成形法、以加熱屡合法或溶媒 2法將各層依單層進行製膜者予以積層並進行加熱虔 =公知方法予以製造’而使用τ,具裝置的擠出成形 法因可使各層膜厚均勾,並可使其寬廣化,故較優良。再 者:於製造寬廣之積層體後,因為可容易切割為符合各式 各樣FPC寬度的寬度’故較適合作為Fpc製造用之離型膜。 本發明之積層體之緩衝層(c)的超出量最好& 2·5職以 下、較佳為0· 1〜2mm、更佳為〇· 5〜2_。Further, 'the surface layer (1) which is at least one outermost layer of the laminated body, the surface roughness Ry丨ub 2G" measured according to JIS B_1, preferably 〇.1~=//111, more preferably 0.1~5/ /111. When the thickness of the surface layer is within the above range, the release property when peeling off the release film after heating and pressurization at the time of FPC production is good. The method for producing the laminate having such a surface roughness is not particularly limited. It can be produced by a known method, and in the extrusion molding method using the τ-mold device, the surface of the cold roller, that is, the surface of the cooling roller is changed by matting treatment, and the surface of the cold light is transferred to (10) After melting the resin, it can be easily cooled, and the thickness of the above range can be easily obtained. Further, after the laminated body having a smooth surface is produced, the laminated body is heated and softened again, and heated and pressurized by an embossing roll. The processing method is to make the surface of the laminated body uniform and rough, and the surface roughness of the object can be obtained. Further, the method for producing the laminated body of the present invention is not particularly limited, and the invention can be borrowed from the 312XP/inventive specification (supplement)/95·〇9 /95116834 24 1294351 2 Using a die-die apparatus extrusion molding method, heating each other by a heating method or a solvent 2 method, a layer is formed by laminating a layer, and heating is performed by a known method. Squeezing of the device The forming method is excellent because it can make the film thickness of each layer be hooked and widened, and further, after manufacturing a wide laminated body, since it can be easily cut into a width corresponding to various FPC widths, It is suitable as a release film for Fpc manufacture. The buffer layer (c) of the laminate of the present invention has an excess amount of & 2.5 or less, preferably 0·1 to 2 mm, more preferably 〇·5~ 2_.

若緩衝層(C)的超出量為上述範圍内,則將本發明積層 體使用作為FPC製造用離型膜的情況下,加熱及加麼時㈢, 緩衝層(c)的超出量較少,可防止因超出之緩衝層(c)附著 於形成有電路之基板或加熱及加墨時使狀金屬板上,而 造成之FPC製品產率降低和作業效率降低等問題。 尚且,緩衝層(C)的超出量,係例如使用3種5層τ一模 具裝置,製造由表面層(Α)/接著層(Β)/緩衝層(c)/接著層 (B)/表面層(A)之5層所構成的寬4〇〇mm的積層體,由任 意位置切出lOcmxlOcm之共計4枚樣品[D2],接著,將[A] 不銹鋼板(32cmx32cmx厚5mm)、[B]作為緩衝材之報紙1〇 張(30cmx30cm)、[C]鋁板(30cmx30cmx 厚 〇· 1_)、[D2]上 述樣品 4 牧,由下依[A]/[B]/[C]/[D2]/[C]/[B]/[A]之順 序重疊。於此,重疊於[C]鋁板上的[D2]樣品4枚,以分 別不重疊的方法排列,接著,於接近使用作為FPC製造用 之離型膜時之加熱及加壓處理條件之溫度l8(rc的環境氣 體中,以壓力8MPa進行加熱及加壓處理1 〇分鐘後,以壓When the excess amount of the buffer layer (C) is within the above range, when the laminated body of the present invention is used as a release film for FPC production, when the heating and the addition are performed (3), the buffer layer (c) has a small excess amount. It is possible to prevent problems such as a decrease in the yield of the FPC product and a decrease in work efficiency due to the excess of the buffer layer (c) attached to the substrate on which the circuit is formed or the metal plate on which the ink is applied during heating and refilling. Further, the excess amount of the buffer layer (C) is produced by, for example, using three kinds of 5-layer τ-die devices, which are manufactured by a surface layer (Α) / an adhesive layer (Β) / a buffer layer (c) / an adhesive layer (B) / surface A layer of 4 mm wide layer composed of 5 layers of layer (A), a total of 4 samples [D2] of 10 cm x 10 cm were cut out from any position, and then [A] stainless steel plate (32 cm x 32 cm x 5 mm thick), [B As a cushioning material, the newspaper 1 sheet (30cmx30cm), [C] aluminum sheet (30cmx30cmx thick 〇·1_), [D2] the above sample 4 grazing, by the bottom [A] / [B] / [C] / [D2 The order of ]/[C]/[B]/[A] overlaps. Here, four [D2] samples superposed on the [C] aluminum plate were arranged so as not to overlap each other, and then the temperature of the heating and pressurization treatment conditions when using the release film for FPC production was as follows. (In the ambient gas of rc, heat and pressurize at a pressure of 8 MPa for 1 minute, then press

312XP/發發明說明書(補件)/95-09/95116834 25 1294351 力5MPa進行保壓,以3分鐘冷 =對取出之4牧樣品,測定從表面層二之端部超=緩 衝層(C)之長度,可求得所得值之最大值。 成 350另至外1〇Γ層體的緩衝量為3°〇…上、較佳為 350至=()()㈣、更佳為.9叫m、特佳為*㈣叫^ 綾衝里右為上述範圍内’則將本發明 =製造㈣型膜之情況下之加熱及㈣時,因為312XP/Inventive Manual (supplement)/95-09/95116834 25 1294351 Force 5MPa for holding pressure, 3 minutes cold = for the 4th grain sample taken out, measured from the end of the surface layer 2 super = buffer layer (C) The length of the obtained value can be obtained. The buffering capacity of the layer of 350 to the outer layer of the layer is 3° 〇..., preferably 350 to = () () (four), more preferably. 9 is called m, especially good is * (four) is called ^ 绫 里The right is within the above range, then the invention will be used in the case of heating (4) in the case of manufacturing a (four) type film, because

(C)具有優越的錄性,故將追隨形成有電路之基板表面 的形狀而良好地變形’可防止形成有電路之基板面與覆蓋 層之間之接著劑的流出,而可防止電路表面被接著劑之^ 所覆蓋,於其後引起之電性連接不良等問題。(C) has excellent visibility, so it will be well deformed following the shape of the surface of the substrate on which the circuit is formed. 'The flow of the adhesive between the substrate surface and the cover layer on which the circuit is formed can be prevented, and the circuit surface can be prevented from being The problem of the electrical connection caused by the subsequent coverage of the agent.

尚且,積層體的緩衝量係例如使用3種5層T-模具裝 置,製造由表面層(A)/接著層(B)八緩衝層(c)/接著 表面層之5層所構成的寬4〇〇_的積層體,由任意位 置切出lOcmxlOcm之共計4枚樣品[D3],接著,將[A]不 銹鋼板(32(:1^32(:„1><厚5_)、[B]作為緩衝材之報紙1〇張 (30cmx30cm)、[C]鋁板(3〇cmx3〇cmx 厚 〇· imm)、[E]具有 lmm0之5處貫通孔之鋁板4枚(75mmx75mmx厚1mm)、[D3] 上 述樣品 4 牧,由下依 [A]/[B]/[C]/[E]/[D3]/[C]/[B]/[A]之順序重疊(於此, 重豐於[C]鋁板上之[E]具有1_0之5處貫通孔之鋁板, 係以分別不重疊之方式排列,又,於[E]具有貫通孔之鋁 板上’將[D 3 ]樣品4枚分別一牧一地枚重疊。) 其次’於溫度170°C之環境氣體中,不加壓(僅有不銹 312XP/發發明說明書(補件)/95-09/95116834 26 1294351 =專之重1)而賴5分鐘後,於溫度17代之環境氣 壓:二 胸加壓2〇秒,於加熱及加壓處理後,以 、、/二^進行保m分鐘冷卻至室溫並取出樣品’ J疋於具有貫通孔之铭板之各貫通孔(共計2G個 的樣品最大長度,計算其平均值則可求得緩衝量。 [離型膜] /本發明之積層體,因於表面層(A)含有4-甲基—I —戊烯 系聚合體,故耐熱性與離型性優越,可使用作為離型膜, 具體可舉例如可撓性印刷電路基板製造用離型膜、航处機 零件所使用之ACM材料用離型膜、硬質印刷電路基板^ 用離3L臈環氧系或酚系等之半導體密封材用離型膜、Μ? 成形用離型膜、橡膝片材硬化用離型膜、特殊黏著膠帶用 之中,使用熱硬化型接著劑,將形成有電路之基板 與復蓋層夾在金屬板中進行加熱及加壓而接著時,為了避 免在加熱及加壓時覆蓋層與金屬板接著的事態,可適合使 用作為夾於其中間而使用之FPC製造用離型膜。 本發明之積層體,因於表面層(A)含有4一甲基—卜戊烯 系t &脰,故耐熱性與離型性優越。又,緩衝層(C)於「pc 製造中加熱及加壓時,因具有優良的柔軟性,故將追隨形 成有電路之基板表面的形狀而良好地變形,可防止形成有 電路之基板面與覆蓋層之間之接著劑的流出。另外,特定 接著劑層(B)以及具有耐熱性樹脂(cl)及軟質樹脂(c2)之 特定組成的緩衝層(C),係加熱及加壓時的超出較少,不 31發發明說明書(補件)/95-09/95116834 27 1294351 致發,因緩衝層⑹附著至形成有電路之基板或用於加熱 及加屋之金屬板上所造成之FPC製品產率降低和作業 =等問題’再者’因為依τ_模具進行之擠出成料輕 易‘造表面粗度與厚薄精度良好之寬廣的膜,故可適 -用作為FPC製造用離型膜。 (實施例) 以下藉貝鈿例更洋細說明本發明,但本發明並不受此 .之任何限制。實施例及比較例中之各物性的評價方法係如 拳下述。 U)熔融流動速率(MFR1) 根據ASTM D1238,以荷重:2.16kg、溫度:23(rc之條 件進行測定。 (2) 熔融流動速率(mfr2) 根據ASTM D1238,以荷重:5kg、溫度:260°C之條件 進行測定。 ' (3) 熔點(Tm) ^ 使用示差掃描量熱計(DSCXPerkinElmer公司製, PYRIS-1型),將試料5mg於氮環境氣體下以28(rc加熱5 •刀知’使其炫融後’以2 〇。〇 /分鐘之降温速度冷卻至室溫, 〜使其結晶化,於室溫保持10分鐘後,求取以1{rc/分鐘 '之升溫速度加熱時之試料的吸熱曲線,以其尖峰溫度表示 熔點。 (4) 加熱及加壓處理前之接著強度 使用3種5層T-模具裝置,將擠出機之設定溫度及τ— 312XP/發發明說明書(補件)/95-09/95116834 28 ⑩ 1294351 模具之設定溫度設為29(TC,藉共擠出製造由表面層(A)/ 接著層(BV緩衝層(〇/接著層(B)/表面層(〇之5 ^所構 成的寬400mm積層體。 ' 其次,根據JIS K6854,從該積層體切出長度150_、 •寬i5mm之樣品,從樣品長度方向之—端,使單側的表面 層(A)稍微剝離,將剝離之表面層(A)、及剝離之表面層(A) 以外之積層體的剩餘部分分別以夾具夾著,以溫度Μ。。、 .剝離角度18〇度、剝離速度300随/分鐘、剝離寬"度15mm 拳之條件進行T子型剝離试驗,測定表面層(a )與緩衝層(匸) 之間的接著強度。 、、 曰 尚且,比較例6及比較例7中,係製造表面層(A)/緩衝 層(C)/表面層(A)之3層所構成的積層體,並與5層之積 層體的情況同樣地進行評價。 9 、 (5)加熱及加壓處理後的接著強度 [加熱及加壓處理] 使用3種5層T-模具裝置,將擠出機之設定溫度及τ— •模具之設定溫度設為290°C,藉共擠出製造由表面層(A)/ -接著層(B)/緩衝層(C)/接著層(B)/表面層(A)之5層所構 •成的寬4〇〇mm積層體,並從該積層體於任意方向切出2〇cm 、x30cm 之樣品[D1 ]。 、 其-人’將[A]不銹鋼板(32cmx32cmx厚5mm)、[B]作為緩 衝材之報紙 10 張(3〇cmx30cm)、[C]鋁板(30cmx30cmx 厚 0.1mm) 、 [D1]上述樣品4牧,由下依 U]/[b]/[c]/[d1]/[c]/[b]/[a]之順序重疊,於溫度 ι8〇 29 312XP/發發明說明書(補件)/95·_5ι聰4 1294351 °c的環境氣體中,以壓力5MPa進行加壓加分鐘,而進行 加熱及加壓處理。接荃,丨v, 接者以壓力5MPa進行保壓,以3分 知冷卻至室溫後,取出樣品。 [接著強度之測定] '將進行加熱及加壓處理所得之樣品的端部lem除去,於 任意方向切出長l50mm、寬15咖之樣品,與上述⑷加埶 及加壓處理前之接著強度測定同樣地進 -驗,測定表面層⑷與緩衝層⑹之間的接著強7:到離°式 拳(6)超出量 & 使用3種5層T-模具裝置,將擠出機之設定溫度及τ一 模,之設定溫度設為29〇t:,藉共擠出製造由表面層⑴/ 接著層(β)/緩衝層(C)/接著層(B)/表面層(A)之5層所構 成的寬400随積層體,並從任意位置方向切出 之樣品。同樣地得到共計4牧的樣品[D2]。 接著,將[A]不銹鋼板(32cmx32cmx厚5mm)、[B]作為緩 衝材之報紙10張(30cmx30cm)、[c]銘板⑽cmx3〇cmx厚 攀〇.1咖)、[D2]上述樣品4牧,由下依 .之順序重疊。於此,重疊 •於[C]鋁板上的[D2]樣品4牧,以分別不重疊的方法排列二 •接著/於溫度l8{rc的環境氣體中,以壓力8MPa加壓 10分鐘,而進行加熱及加壓處理後,以壓力5MPa進行保 壓’以3分鐘冷卻至室溫並取出樣品。 超出量係測定從取出之4牧樣品之表面層(〇端部超出 的緩衝層(C)之長度,以其之最大值作為超出量。 312XP/發發明說明書(補件)/95-09/95116834 30Further, the buffer amount of the laminate is, for example, a width of 4 layers of the surface layer (A) / the adhesion layer (B) eight buffer layer (c) / the surface layer 5 layers, using three kinds of 5-layer T-die devices. For the layered body of 〇〇_, a total of 4 samples [D3] of lOcmxlOcm are cut out from any position, and then [A] stainless steel plate (32 (: 1^32 (: 1 >< thick 5_), [B As a cushioning material, the newspaper 1 sheet (30cmx30cm), [C] aluminum sheet (3〇cmx3〇cmx thick 〇·imm), [E] 4 sheets of aluminum plate with 5mm through holes of 1mm0 (75mmx75mmx thickness 1mm), [ D3] The above sample 4 is grazing, and overlaps in the order of [A]/[B]/[C]/[E]/[D3]/[C]/[B]/[A] [E] The aluminum plate having the through hole of 1_0 at [C] on the aluminum plate is arranged so as not to overlap, and the [D 3 ] sample is placed on the aluminum plate having the through hole [E] One animal and one land overlap each other.) Secondly, in the ambient gas at a temperature of 170 ° C, no pressure (only stainless 312XP / invention manual (supplement) / 95-09/95116834 26 1294351 = special weight 1) After 5 minutes, the ambient pressure at the temperature of 17 generations: 2 chest pressure 2 sec seconds, heating and adding After the treatment, the mixture was cooled to room temperature with m, m, and m, and the sample was taken out. Each of the through holes of the nameplate with the through holes (the total length of the sample of 2G totals was calculated, and the average value was calculated to obtain the buffer. [Separation film] / The laminate of the present invention, since the surface layer (A) contains a 4-methyl-I-pentene polymer, it is excellent in heat resistance and release property, and can be used as a release film. Specifically, for example, a release film for producing a flexible printed circuit board, a release film for ACM materials used in aeronautical machine parts, and a semiconductor printed circuit board for a hard printed circuit board, such as a 3L epoxy or a phenol system. For the release film, the release film for forming, the release film for the rubber sheet for sheeting, and the special adhesive tape, the circuit-formed substrate and the cover layer are sandwiched by a thermosetting adhesive. In the case of heating and pressurizing the metal plate, in order to avoid the situation in which the coating layer and the metal plate are in contact with each other during heating and pressurization, a release film for FPC production which is used as a sandwich between them can be suitably used. Laminated body due to surface layer (A) containing 4-methyl -Bupentene is a kind of t & 脰, so it is excellent in heat resistance and release property. Moreover, when the buffer layer (C) is heated and pressurized in the manufacture of pc, it has excellent flexibility, so it will follow the circuit. The shape of the surface of the substrate is well deformed, and the outflow of the adhesive between the substrate surface on which the circuit is formed and the cover layer can be prevented. Further, the specific adhesive layer (B) and the heat resistant resin (cl) and the soft resin ( The buffer layer (C) of the specific composition of c2) is less excessively heated and pressurized, and is not caused by the invention (supplement)/95-09/95116834 27 1294351, because the buffer layer (6) adheres to the formation. The problem of the yield reduction of the FPC product and the operation of the FPC product caused by the circuit board or the metal plate for heating and adding the 'furrow' is easy to make the surface roughness due to the extrusion of the material by the τ_mold. A wide film with good thickness and precision is suitable for use as a release film for FPC manufacturing. (Embodiment) Hereinafter, the present invention will be described more specifically by way of examples, but the present invention is not limited thereto. The evaluation methods of the physical properties in the examples and comparative examples are as follows. U) Melt flow rate (MFR1) Measured according to ASTM D1238 with a load of 2.16 kg and a temperature of 23 (rc). (2) Melt flow rate (mfr2) According to ASTM D1238, load: 5 kg, temperature: 260° The conditions of C were measured. ' (3) Melting point (Tm) ^ Using a differential scanning calorimeter (manufactured by DSCXPerkinElmer, PYRIS-1 type), 5 mg of the sample was heated under a nitrogen atmosphere of 28 (rc heating 5 • knife knowing ' After smelting, it was cooled to room temperature at a cooling rate of 2 〇.〇/min, crystallization was allowed, and it was kept at room temperature for 10 minutes, and then heated at a heating rate of 1{rc/min'. The endothermic curve of the sample indicates the melting point at its peak temperature. (4) The strength before the heating and pressure treatment is performed using three 5-layer T-die devices, and the set temperature of the extruder and the τ-312XP/inventive specification ( Replenishment) / 95-09/95116834 28 10 1294351 The set temperature of the mold is set to 29 (TC, manufactured by co-extrusion from the surface layer (A) / subsequent layer (BV buffer layer (〇 / adhesion layer (B) / surface Layer (a width of 400 mm formed by 5 ^ 〇. ' Second, according to JIS K6854, cut from the layer A sample having a length of 150 mm and a width of i5 mm is slightly peeled off from the one end side of the sample, and the surface layer (A) on one side is peeled off, and the surface layer (A) which is peeled off and the layered body other than the peeled surface layer (A) are laminated. The remaining part was clamped by a clamp, and the surface layer was measured by a temperature Μ, . . . peeling angle of 18 、, peeling speed of 300 with / minute, peeling width " degree 15 mm punching condition, T-type peeling test a) the bonding strength between the buffer layer (匸), and the third layer of the surface layer (A)/buffer layer (C)/surface layer (A) in Comparative Example 6 and Comparative Example 7 The laminated body thus formed was evaluated in the same manner as in the case of the laminated body of five layers. 9. (5) Adhesive strength after heating and pressure treatment [heating and pressurization treatment] Three kinds of five-layer T-die devices were used. The set temperature of the extruder and the set temperature of the τ--mold are set to 290 ° C, and the surface layer (A) / - the subsequent layer (B) / the buffer layer (C) / the subsequent layer are manufactured by co-extrusion ( B) / The width of 4 layers of the surface layer (A) is 4 mm thick, and the thickness of the laminate is 2 〇 cm, x 30 cm in any direction. Sample [D1]., -People's [A] stainless steel plate (32cmx32cmx thickness 5mm), [B] as a cushioning material newspaper 10 sheets (3〇cmx30cm), [C] aluminum plate (30cmx30cmx thickness 0.1mm), [ D1] The above sample 4 is grazing, and is superimposed in the order of U]/[b]/[c]/[d1]/[c]/[b]/[a] at the temperature ι8〇29 312XP/ (Supply) / 95 · _5 ι 聪 4 1294351 °c of the ambient gas, pressurization plus 5 minutes at a pressure of 5 MPa, and heating and pressure treatment. After the connection, 丨v, the pressure is maintained at a pressure of 5 MPa, and after cooling to room temperature at 3 minutes, the sample is taken out. [Measurement of Strength Next] 'The end portion lem of the sample obtained by heating and pressurizing treatment was removed, and a sample having a length of l50 mm and a width of 15 coffee was cut out in any direction, and the bonding strength before the above (4) twisting and pressurization treatment was performed. The measurement was carried out in the same manner, and the adhesion between the surface layer (4) and the buffer layer (6) was measured. 7: The amount of excess from the ° boxing (6) & The setting of the extruder was carried out using three 5-layer T-die devices. Temperature and τ, the set temperature is set to 29〇t:, by coextrusion manufacturing by surface layer (1) / subsequent layer (β) / buffer layer (C) / subsequent layer (B) / surface layer (A) The five layers are formed with a width of 400 and a sample which is cut out from any position. A total of 4 grazing samples [D2] were obtained in the same manner. Next, [A] stainless steel plate (32cmx32cmx thickness 5mm), [B] as a cushioning material newspaper 10 sheets (30cmx30cm), [c] nameplate (10) cmx3〇cmx thick climbing. 1 coffee), [D2] above sample 4 animal husbandry , overlapping by the order of the next. Here, the [D2] sample 4 on the [C] aluminum plate was superimposed and arranged in a non-overlapping manner, and then subjected to pressure at a pressure of 8 MPa for 10 minutes in an ambient gas at a temperature of 8 8 rc. After the heating and pressure treatment, the pressure was maintained at a pressure of 5 MPa. The mixture was cooled to room temperature in 3 minutes and the sample was taken out. The excess amount is determined from the surface layer of the removed 4 samples (the length of the buffer layer (C) beyond the end of the crucible, and the maximum value thereof is used as the excess amount. 312XP/Inventive Manual (Supplement)/95-09/ 95116834 30

1294351 (Ό緩衝量 使用3種5層Τ-模具裝置,將擠出機之設定溫度及τ一 模具之設定溫度設為290°C,藉共擠出製造由表面層(Α)/ 接著層(Β)/緩衝層(C)/接著層(Β)/表面層(a)之5層所構 -·成的寬400mm積層體,並從任意位置切出1〇cmxl〇cm之樣 品。同樣地得到共計4牧的樣品[D3]。 接著’將[A]不銹鋼板(32cmx32cmx厚5mm)、[B]作為緩 •衝材之報紙 張(30cmx30cm)、[C]鋁板(30cmx30cmx 厚 參〇· 1mm)、[E]具有1_0之5處貫通孔之鋁板4枚(75_χ 75mm X厚1mm)、[D3]上述樣品4牧,由下依 U]/[B]/[C]/[E]/[D3]/[C]/[B]/[A]之順序重疊。於此, 重豐於[C]鋁板上之[E]具有1_必之5處貫通孔之鋁板, 係以分別不重疊之方式排列,又,於[E]具有貫通孔之鋁 板上’將[D 3 ]樣品4牧分別一牧一牧重疊。 其次,於溫度17(TC之環境氣體中,不加壓(僅有不銹 鋼板等之重量)而預熱5分鐘後,於溫度17(rC2環境氣 _體下,以壓力5MPa加壓20秒,於加熱及加壓處理後,以 壓力5MPa進行保壓,以3分鐘冷卻至室溫並取出樣品。 ‘ 緩衝量係測定於具有貫通孔之鋁板之各貫通孔(共計2〇 -個)所垂下的樣品最大長度,求取其平均值作為緩衝量。 .(8)面粗度 於切出為lOcmxlOcmx厚度100//m之尺寸的測定試料 中,以從中心於任意方向上之5cm作為基準長度,以根據 JIS B0601之方法,針對積層體最外層之表面層之任 312XP/發發明說明書(補件)/95-09/95116834 31 1294351 思一表面,求得面粗度Ry。 [實施例1 ] 〈表面層(A)&gt; 使用4一曱基—1-戊烯系共聚合體[1-癸烯含有量:6質量1294351 (The amount of buffer is three layers of Τ-die device, and the set temperature of the extruder and the set temperature of the τ-die are set to 290 ° C, and the surface layer (Α)/ subsequent layer is produced by co-extrusion ( Β) / buffer layer (C) / adhesion layer (Β) / surface layer (a) of the five layers of the formation of a width of 400mm laminate, and cut from any position 1〇cmxl〇cm sample. A total of 4 grazing samples [D3] were obtained. Next, [A] stainless steel plate (32 cm x 32 cm x 5 mm thick), [B] was used as a slow-cut sheet (30 cm x 30 cm), [C] aluminum plate (30 cm x 30 cm x thick 〇 〇 1 mm ), [E] 4 pieces of aluminum plate with 5 to 1 through holes of 1_0 (75_χ 75mm X thickness 1mm), [D3] above sample 4, by U]/[B]/[C]/[E]/ The order of [D3]/[C]/[B]/[A] overlaps. Here, the [E] has an aluminum plate with 1 through-holes of 5 holes on the [C] aluminum plate, respectively Arranged in an overlapping manner, and in [E] aluminum plate with through-holes, '[D 3 ] sample 4 grazing, grazing, grazing, and grazing. Second, at temperature 17 (TC ambient gas, no pressure (only There is a weight of stainless steel, etc.) and after preheating for 5 minutes, at a temperature of 17 (rC2 ambient gas _ body After pressurizing at a pressure of 5 MPa for 20 seconds, after heating and pressurizing treatment, the pressure was maintained at a pressure of 5 MPa, and the sample was taken out by cooling to room temperature for 3 minutes. The buffer amount was measured in each through hole of the aluminum plate having the through hole. (Total 2 〇-pieces) The maximum length of the sample to be dropped, and the average value is taken as the buffer amount. (8) The surface roughness is measured in a sample having a thickness of 100 cm/m cut to a thickness of 100 cm/cm. 5cm in any direction as the reference length, in accordance with the method of JIS B0601, for the surface layer of the outermost layer of the laminated body, 312XP / invention manual (supplement) / 95-09/95116834 31 1294351 Surface roughness Ry [Example 1] <Surface layer (A)> Using 4-mercapto- 1-pentene copolymer [1-decene content: 6 mass

• %’ 溶點·· 228°C,MFR2·· 26g/10 分鐘,密度·· 835kg/m3(ASTM D1505)]。 〈接著層(B)&gt; (b1) —a ·· 4-曱基-1-戊烯系共聚合體[1-癸烯含有量:3 拳質量%,MFR2 ·· 5g/l〇分鐘]35質量%。 (b2-1)乙烯·卜丁烯無規共聚合體[EBR,卜丁烯含有 ® : 15 質量 %,MFR1 : 7g/l〇 分鐘]15 質量 %。 (b2 —2)1 —丁烯•乙烯無規共聚合體[PB-1,乙烯含有量: W 質量 %,MFR1 : 〇· 4g/l〇 分鐘]5〇 質量 %。 相對於上述之(bl)-a、(b2-1)及(b2-2)的合計100質量 份,再添加肆[亞甲基—3-(3,5 —二—第三丁基-4—羥苯基) 丙酉夂g曰]甲烧(Chiba Specialty Chemicals(股)製,商品 名Irganox 1 01 〇」)〇 · 10質量份、及硬脂酸鈣(三共有機 合成(股),商品名硬脂酸鈣)〇· 〇3質量份作為安定劑,使 •=漢歇爾混合器進行乾式摻合。其次,將所得混合物以設 ' f為28〇它之65_必之雙軸擠出機進行熔融混練,調製接 - 者性的樹脂組成物。 〈緩衝層(C ) &gt; (cl)-a:作為熔點19(rc以上之耐熱性樹脂,使用盥表 面層(A)相同之4-甲基戊烯系共聚合體2〇質量%。 312XP/發發明說明書(補件)/95-09/95116834 32 1294351 ,⑽-a:作為炫,點17〇μ下之軟質樹脂,使用低密度 4乙稀[溶點:11(TC,MFRi : 2 〇g/1〇分鐘,密度: 920kg/m3(ASTM D1 505)]80 質量%。 其次,將上述(cl)—a及(c2)—a使用漢歇爾混合器進行 - 乾式摻合。 〈積層體之製造〉 、四使用附有3種5層T-模具之擠出冑,將擠出機之設定 •度度及T—杈具之設定溫度設為290°C,藉共擠出製造由表 拳面層(A)/接著層(b)/緩衝層(c)/接著層表面層(A)之 5、層所構成的見40〇mm積層體。將所得之積層體的厚度構 成及各物性值的評價結果示於表1 —丨。 另外,僅使用接著層(B)之擠出機使接著層之單層膜 進行成开y,測疋所得膜之荷重2· 16kg、溫度之熔融 流動速率,而測定接著層(…之MFRl。 “同樣地僅使用緩衝層(c)之擠出機使緩衝層(c)之單層 膜進订成形,測定所得膜之荷重2· 16kg、溫度23(rc之熔 籲融流動速率,而測定緩衝層(〇之MFRl。結果示於表pi。 •[實施例2 ] 〈表面層(A)&gt; ··使用與實施例1相同之4-曱基-1-戊烯系共聚合體。 _ 〈接著層(B)&gt; 使用與實施们相$之接著性樹月旨組成物。 〈緩衝層(C)&gt; (cl)-a ·作為:):容點19〇〇c以上之耐熱性樹脂,使用與實 312Xp/發發明說明書(補件)/95·〇9/95!16834 1294351 施例1相同之4-甲基-1-戊烯系共聚合體3〇質量%。 (c2)-a ·作為熔點170°C以下之軟質樹脂,使用與實施 例1相同之低密度聚乙烯70質量%。 /'、 •其次,將上述(cl) 一a及(c2)—a使用漢歇爾混合器 • 乾式摻合。 〈積層體之製造〉 使用3種5層T-模具裝置,將擠出機之設定溫度及 •模具之設定溫度設為290。〇,藉共播出製造由表面層(A)〆 •接著層(Β)/緩衝層(C)/接著層⑻/表面層⑴之5層所構 成的寬權賴積層體。將所得之積層體的厚㈣成及各物 性值的評價結果示於表1 - 1。 與實施例1同樣地,將接著層⑻及緩衝層⑹之單層膜 分別進行成形,測定MFR1。結果示於表卜丨。 、 [實施例3] 〈表面層(A)&gt; 使用與實施例1相同之4_曱基一卜戊烯系共聚合體。 _ &lt;接著層(B)&gt; &quot; 使用與實施例1相同之接著性樹脂組成物。 •〈緩衝層(C)之樹脂組成物&gt; 〜(cl)_a:作為熔點19(TC以上之耐熱性樹脂,使用鱼 、施例1相同之4一甲基-1-戊烯系共聚合體40質量%。、、 (c2)-am點17代以下之軟質樹脂,使用與 例1相同之低密度聚乙烯6〇質量%。 、 其-人’將上述(cl)-a及(。2)一a使用漢歇爾混合器進行 34 312XP/發發明晒書(補件)/95-09/95116834• %' melting point · · 228 ° C, MFR 2 · · 26 g / 10 min, density · · 835 kg / m3 (ASTM D1505)]. <Next layer (B)&gt; (b1) —a ·· 4-mercapto-1-pentene-based copolymer [1-ceene content: 3% by mass, MFR2 ··5g/l〇 minutes] 35 quality%. (b2-1) Ethylene-butene random copolymer [EBR, butene-containing ® : 15% by mass, MFR1: 7 g/l 〇 minute] 15% by mass. (b2-2) 1-butene/ethylene random copolymer [PB-1, ethylene content: W mass %, MFR1 : 〇·4g/l 〇 minute] 5 〇 mass %.肆[methylene-3-(3,5-di-t-butyl-4) is further added to 100 parts by mass of the above-mentioned (bl)-a, (b2-1) and (b2-2). -Hydroxyphenyl) propyl hydrazine 曰 甲 甲 ( ( ( Chi Chi Chi Chi Chi Chi Chi Chi Chi Chi Chi Chi 10 10 10 10 10 10 10 10 10 10 10 10 10 10 10 10 10 10 10 10 10 10 10 10 10 10 10 10 10 10 10 10 The product name is calcium stearate) 〇· 〇 3 parts by mass as a stabilizer, and the •= Hanschel mixer is dry blended. Next, the obtained mixture was melt-kneaded by a twin-screw extruder having a 'f of 28 Å, which was a must-have, and a resin composition was prepared. <Cushion layer (C) &gt; (cl)-a: As a heat-resistant resin having a melting point of 19 or more, a 4-methylpentene-based copolymer having the same surface layer (A) is used in an amount of 2% by mass. 312XP/ Invention specification (supplement) / 95-09/95116834 32 1294351 , (10)-a: as a soft resin with a point of 17 〇μ, using a low density of 4 ethylene [melting point: 11 (TC, MFRi: 2 〇) g/1 minute, density: 920 kg/m3 (ASTM D1 505)] 80% by mass. Next, the above (cl)-a and (c2)-a were subjected to dry blending using a Hanschel mixer. Manufacture of the body>, four use the extrusion 胄 with three kinds of 5-layer T-die, set the degree of the extruder and the set temperature of the T-cooker to 290 °C, by co-extrusion manufacturing The face punch layer (A) / the subsequent layer (b) / the buffer layer (c) / the layer of the layer (A) of the layer of the layer of the layer of the layer of the surface layer (A) The evaluation results of the respective physical property values are shown in Table 1. In addition, the single layer film of the adhesive layer was opened to open y using only the extruder of the adhesive layer (B), and the load of the obtained film was measured to be 2·16 kg, and the temperature was measured. Melt flow rate, and The MFR1 of the adhesive layer (...) was similarly used. The single layer film of the buffer layer (c) was formed by extrusion using only the buffer layer (c), and the load of the obtained film was measured to be 2·16 kg and the temperature was 23 (rc). The melt flow rate was measured, and the buffer layer (MFR1 of 〇 was measured. The results are shown in Table pi. • [Example 2] <Surface layer (A)> The same 4-mercapto-1 as in Example 1 was used. - pentene-based copolymer. _ <Next layer (B)&gt; The composition of the conjugated tree with the implementer is used. <Buffer layer (C)&gt; (cl)-a · As:): For a heat-resistant resin having a temperature of 19 〇〇c or more, the same 4-methyl-1-pentene copolymer as in Example 1 of the invention (Supplement) / 95·〇9/95! 16834 1294351 (c2)-a - As a soft resin having a melting point of 170 ° C or less, 70% by mass of the low-density polyethylene similar to that of Example 1 is used. /', • Next, the above (cl) a and (c2)—a uses a Hanschel mixer • Dry blending. <Manufacturing of laminated body> Using three 5-layer T-die devices, the set temperature of the extruder and the set temperature of the mold are set to 290. ,borrow Broadcasting and manufacturing a wide-weight laminated body composed of five layers of the surface layer (A), the back layer (Β)/the buffer layer (C)/the back layer (8)/the surface layer (1). The thickness of the obtained laminate is (4) The evaluation results of the physical property values and the respective physical property values are shown in Table 1-1. In the same manner as in Example 1, the single layer films of the adhesive layer (8) and the buffer layer (6) were each molded, and MFR1 was measured. The results are shown in the table. [Example 3] <Surface layer (A)&gt; The same 4_mercapto-p-pentene-based copolymer as in Example 1 was used. _ &lt;Next layer (B)&gt;&quot; The same adhesive resin composition as in Example 1 was used. <Resin composition of buffer layer (C)>~(cl)_a: As a heat-resistant resin having a melting point of 19 (TC or more, fish, the same 4-methyl-1-pentene copolymer of the same example 1 was used. 40% by mass, and (c2)-am, the soft resin of 17 or less generations, the same low density polyethylene as in Example 1 was used in an amount of 6% by mass. The same as the above-mentioned (cl)-a and (.2) ) a a Hansler mixer for 34 312XP / hair invented the book (supplement) / 95-09/95116834

1294351 乾式播合。 〈積層體之製造〉 使用3種5層T-模具裝置,將擠出機之設定溫度及Τ-模具之設定溫度設為290C ’藉共擠出製造由表面層(a)/ 接著層(B)/缓衝層(C)/接著層(B)/表面層(A)之5層所構 成的寬400mm積層體。將所得之積層體的厚度構成及各物 性值的評價結果示於表1 — 1。 • 又,與實施例1同樣地,將接著層(B )及緩衝層(c)之單 拳層膜分別進行成形,測定MFR1。結果示於表卜i。 [實施例4] 〈表面層(A)&gt; 使用與實施例1相同之4-曱基-1-戊烯系共聚合體。 〈接著層(B)&gt; 使用與實施例1相同之接著性樹脂組成物。 〈緩衝層(C)&gt; (cl)-b ·作為熔點19〇 °c以上之耐熱性樹脂,使用聚醯 _胺6[三菱工程塑膠(股)製,商品名「N〇vamidl020C」,熔 •點:218°C,MFR2 : 35g/10 分鐘]20 質量 〇/〇。 • (c2) —a :作為熔點170°C以下之軟質樹脂,使用與實施 例1相同之低密度聚乙烯60質量%。 〜 (c2)—b :使用順丁烯二酸改質低密度聚乙烯[順丁烯二 酸肝含有率(改質率)〇· 2重量%,熔點:l〇9°C,MFR1 : 2· 6g/10 分鐘,密度:920kg/m3(ASTM D1505)]20 質量 0/〇。 其次’將上述(cl)一b、(c2)一a及(c2)一b使用漢歇爾混 312XP/發發明說明書(補件)/95-09/95116834 35 1294351 合器進行乾式摻合。 〈積層體之製造〉 使用3種5層T-模具裝置,將擠出機之設定溫度及τ-模具之設定溫度設為290 °C,藉共擠出製造由表面層(A)/ 接著層(B)/緩衝層(C)/接著層(B)/表面層(A)之5層所構 成的寬400mm積層體。將所得之積層體的厚度構成及各物 性值的評價結果示於表1-1。 • 又,與實施例1同樣地,將接著層(B)及缓衝層(C)之單 參層膜分別進行成形,測定MFR1。結果示於表1 — 1。 [實施例5 ] 〈表面層(A)&gt; 使用與實施例1相同之4-曱基-1-戊烯系共聚合體。 〈接著層(B)&gt; 使用與實施例1相同之接著性樹脂組成物。 〈緩衝層(C)&gt;1294351 Dry sowing. <Manufacturing of laminated body> Using three kinds of five-layer T-die devices, the set temperature of the extruder and the set temperature of the Τ-mold were set to 290C'. By co-extrusion, the surface layer (a) / the subsequent layer (B) / 400 layers of a buffer layer (C) / 5 layers of the layer (B) / surface layer (A). The thickness constitution of the obtained laminate and the evaluation results of the respective physical properties are shown in Table 1-1. Further, in the same manner as in the first embodiment, the single layer films of the adhesive layer (B) and the buffer layer (c) were separately molded, and MFR1 was measured. The results are shown in Table i. [Example 4] <Surface layer (A)&gt; The same 4-mercapto-1-pentene copolymer was used as in Example 1. <Adhesion layer (B)&gt; The same adhesive resin composition as in Example 1 was used. <Cushion layer (C)&gt; (cl)-b · As a heat-resistant resin having a melting point of 19 〇 ° or more, it is made of polyfluorene-amine 6 [Mitsubishi Engineering Plastics Co., Ltd., trade name "N〇vamidl020C", melting • Point: 218 ° C, MFR 2 : 35 g / 10 min] 20 mass 〇 / 〇. (c2) - a : As a soft resin having a melting point of 170 ° C or less, 60% by mass of the same low-density polyethylene as in Example 1 was used. ~ (c2)-b : using maleic acid modified low density polyethylene [hepatic acid content (modified rate) 〇 · 2% by weight, melting point: l〇9 ° C, MFR1 : 2 · 6g/10 minutes, density: 920kg/m3 (ASTM D1505)] 20 mass 0/〇. Next, the above (cl)-b, (c2)-a and (c2)-b were dry blended using Hanschel Blend 312XP/Inventive Manual (Supplement)/95-09/95116834 35 1294351. <Manufacturing of laminated body> Using three kinds of five-layer T-die devices, the set temperature of the extruder and the set temperature of the τ-mold were set to 290 °C, and the surface layer (A)/layer was produced by co-extrusion. (B) / Buffer layer (C) / Adhesion layer (B) / Surface layer (A) 5 layers of a wide 400mm laminate. The thickness constitution of the obtained laminate and the evaluation results of the respective physical properties are shown in Table 1-1. Further, in the same manner as in Example 1, the single-layer film of the adhesive layer (B) and the buffer layer (C) was separately molded, and MFR1 was measured. The results are shown in Table 1-1. [Example 5] <Surface layer (A)&gt; The same 4-mercapto-1-pentene copolymer was used as in Example 1. <Adhesion layer (B)&gt; The same adhesive resin composition as in Example 1 was used. <buffer layer (C)&gt;

(cl)-c :作為熔點19(rc以上之耐熱性樹脂,使用聚醯 胺6[三菱工程塑膠(股)製,商品名rN〇vamidl〇ucH5」, 炫點:219 C,MFR2 : 170g/10 分鐘]2〇 質量%。 (c2)-a ·作為熔點170°C以下之軟質樹脂,使用與實施 例1相同之低密度聚乙烯60質量%。 貝也 (c2)-b :使用順丁烯二酸改f聚乙烯[順τ烯二酸 有率(改質率)0.2重量%,熔點:1〇9。〇,MFR1: 2 6g/i〇 其次,將上述(Cl)-C、 (c2)-a及(C2)-b使用漢歇爾混 36 312XP/發發明說明書(補件)/95-09/95116834 ⑩ 1294351 合器進行乾式摻合。 〈積層體之製造〉 使用3種5層T-模具裝置,將擠出機之設定溫度及T— ~模具之設定溫度設為290°C,藉共擠出製造由表面層(Α)/ •接著層(B)/緩衝層(〇/接著層(B)/表面層(A)之5層所構 成的寬400_積層體。將所得之積層體的厚度構成及各物 性值的評價結果示於表1 —J。 • 又,與實施例1同樣地,將接著層(B)及緩衝層(C)之單 參層膜分別進行成形,測定MFRi。結果示於表14。 [實施例6 ] 〈表面層(A)&gt; 使用與實施例1相同之4-甲基-1 一戊烯系共聚合體。 〈接著層(B)&gt; 使用與實施例1相同之接著性樹脂組成物。 〈緩衝層(C)&gt; (cl)-a:作為熔點19(rc以上之耐熱性樹脂,使用盥每 施例1相同之4-甲基-戊烯系共聚合體3〇質量%。、、 (心:作為溶點⑽以下之軟質樹月卜使用丙烯· 卜丁烯無規共聚合體[丨―丁烯含有量:25質量% 110°c,MFR1 ·· 6· Og/10 分鐘]70 質量%。 ” · 其次,將上述(cl)_a、(c2)-c使用、BA r a 乾式摻合。 ❹錢_混合器進行 〈積層體之製造〉 使用3種5層T-模具裝置,將擠出擔 佾铖之設定溫度及 312XP/發發明說明書(補件)/95-09/95116834 37(cl)-c : As a heat-resistant resin having a melting point of 19 (rc or more, polyamine 6 [Mitsubishi Engineering Plastics Co., Ltd., trade name rN〇vamidl〇ucH5", Hyun: 219 C, MFR2: 170 g/ 10 minutes] 2% by mass. (c2)-a - As a soft resin having a melting point of 170 ° C or less, 60% by mass of the low-density polyethylene similar to that of Example 1 was used. Belle (c2)-b: using cis-butyl The enedionic acid is changed to f polyethylene [the yield of the cis- enedenedioic acid (modification rate) 0.2% by weight, the melting point: 1〇9. 〇, MFR1: 2 6g/i 〇 followed by the above (Cl)-C, ( C2)-a and (C2)-b use Hanscher Mix 36 312XP/Inventive Manual (Supplement)/95-09/95116834 10 1294351 for dry blending. <Manufacture of laminated body> Use 3 kinds of 5 The layer T-mold device sets the set temperature of the extruder and the set temperature of the T-~mold to 290 ° C, and is manufactured by co-extrusion from the surface layer (Α) / • the subsequent layer (B) / buffer layer (〇 / The layer 400-layer of the layer of the layer (B) / the surface layer (A) is formed. The thickness of the obtained layered body and the evaluation results of the physical properties are shown in Table 1 - J. Embodiment 1 is similarly The single-layer film of the layer (B) and the buffer layer (C) was separately molded, and MFRi was measured. The results are shown in Table 14. [Example 6] <Surface layer (A)> The same as Example 1 was used. Methyl-1 monopentene copolymer. <Back layer (B)&gt; The same adhesive resin composition as in Example 1 was used. <Buffer layer (C)> (cl)-a: As melting point 19 ( The heat-resistant resin of rc or more is used in an amount of 3% by mass of the 4-methyl-pentene-based copolymer which is the same as in Example 1. (Heart: soft ash as a melting point (10) or less. Alkene random copolymer [丨-butene content: 25 mass% 110 ° C, MFR1 ··6·Og/10 min] 70 mass%. ” · Next, the above (cl)_a, (c2)-c Use, BA ra dry blending. ❹ _ _ mixer to manufacture <layered body> Using three kinds of five-layer T-mold device, the set temperature of the extrusion and 312XP / invention manual (supplement) / 95-09/95116834 37

1294351 模^之設定溫度設為29(rc,藉共擠出製造由表面層(A)/ 接著層(B)/緩衝層(C)/接著層(B)/表面層(4)之5層所構 成的寬400mm積層體。將所得之積層體的厚度構成及各物 “ 性值的評價結果示於表1 一2。 -· 又,與實施例1同樣地,將接著層(B)及缓衝層(C)之單 層膜分別進行成形,測定MFRi。結果示於表1-2。 [實施例7] ,〈表面層(A)&gt; _ 使用與實施例1相同之曱基-1-戊烯系共聚合體。 〈接著層(B)&gt; 使用與實施例1相同之接著性樹脂組成物。 〈緩衝層(C)&gt; (cl)-a ·作為熔點190 °C以上之耐熱性樹脂,使用與實 施例1相同之4-曱基-1 -戊烯系共聚合體丄5質量%。 (c2)-d :作為熔點n〇°C以下之軟質樹脂,使用丙烯均 聚合體[熔點:16(TC,MFR1 : 2.0g/l〇分鐘]85質量%。 •其次,將上述(cl)一a、(c2)—d使用漢歇爾混合器進行 - 乾式摻合。 .〈積層體之製造〉 、 使用3種5層T-模具裝置,將擠出機之設定溫度及丁一 —模具之設定溫度設為290°C,藉共擠出製造由表面層(A)/ 接著層(B)/緩衝層(〇/接著層(B)/表面層(A)之5層所構 成的寬400mm積層體。將所得之積層體的厚度構成及各物 性值的評價結果示於表1 —2。 312XP/發發明說明書(補件)/95-09/95116834 38 1294351 又,與實施例1同樣地,將接著層〇)及緩衝層(c)之單 層膜分別進行成形,測定MFR1。結果示於表1 — 2。 [實施例8] “〈表面層(A)&gt; 使用與實施例1相同之4-甲基-1-戊烯系共聚合體。 〈接著層(B)&gt; 使用與實施例1相同之(bl)_a、α2_η、(b2_2),使用 . 以下組成比之接著性樹脂組成物。 9 (bl)-a· 4甲基-1-戊稀系共聚合體2〇質量%。 (b2-l):乙烯· 1-丁烯無規共聚合體3〇質量%。 (b2-2) : 1-丁烯•乙烯無規共聚合體5〇質詈 〈緩衝層(C)&gt; ' 與實施例2同樣地,將(ci)-a設為3〇質量%、(c2)-a 設為70質量%,使用漢歇爾混合器進行乾式摻合。 〈積層體之製造〉 使用3種5層T-模具裝置,將擠出機之設定溫度及τ一 •模具之設定溫度設為290X:,藉共擠出製造由表面層(A)/ «接者層(B)/缓衝層(C) /接者層(B) /表面層(a)之5層所構 •成的寬400mm積層體。將所得之積層體的厚度構成及各物 、 性值的評價結果示於表1-2。 又與實施例1同樣地,將接著層(B)及緩衝層(c)之單層 膜分別進行成形’測定MFR1。結果示於表1__2。 [實施例9] 〈表面層(A)&gt; 312XP/發發明說明書(補件)/95_〇9/95116834 39 1294351 使用與實施例 〈接著層(B)&gt; 1相同之4-曱基 一卜 戊烯系 共聚合體。 (b2〜1)、(b2-2),使用 使用與實施例1相同之(bl)—a 以下組成比之接著性樹脂組成物 癸烯含有量 (bl)-a : 4-曱基-1-戊烯系共聚合體 質量%,MFR2 ·· 5g/10分鐘]50質量%。 (b2-l)··乙烯· 1-丁烯無規共聚合體[ebr,卜丁烯含有 量:15 質量 % ’ MFR1 : 7g/l〇 分鐘](b2) 1〇 質量 %。1294351 The setting temperature of the mold is set to 29 (rc, manufactured by co-extrusion from the surface layer (A) / the subsequent layer (B) / the buffer layer (C) / the subsequent layer (B) / the surface layer (4) The thickness of the laminate of the above-mentioned laminate is shown in Table 1 to 2. The thickness of the obtained laminate and the evaluation results of the respective properties are shown in Table 1 - 2. In addition, in the same manner as in the first embodiment, the adhesive layer (B) and The single layer film of the buffer layer (C) was separately molded, and MFRi was measured. The results are shown in Table 1-2. [Example 7], <Surface layer (A)> _ The same thiol group as in Example 1 was used - 1-Pentylene-based copolymer. <Adhesion layer (B)&gt; The same adhesive resin composition as in Example 1 was used. <Buffer layer (C)> (cl)-a · As a melting point of 190 ° C or higher The heat resistant resin was used in an amount of 5% by mass of the 4-mercapto-1 -pentene copolymer in the same manner as in Example 1. (c2)-d: a soft resin having a melting point of n〇 ° C or less, and a propylene homopolymer was used. [Melting point: 16 (TC, MFR1: 2.0 g/l 〇 minute) 85 mass%. • Next, the above (cl)-a, (c2)-d was subjected to dry blending using a Hanschel mixer. Manufacture of laminates Three kinds of 5-layer T-die devices, the set temperature of the extruder and the set temperature of the die-die are set to 290 ° C, and the surface layer (A) / the subsequent layer (B) / buffer layer are manufactured by co-extrusion. (a 400 mm wide layered product composed of five layers of 〇/sublayer (B)/surface layer (A). The thickness of the obtained laminate and the evaluation results of the physical property values are shown in Table 1-2. 312XP/fat In the same manner as in the first embodiment, a single layer film of the underlayer layer and the buffer layer (c) was molded, and MFR1 was measured. The results are shown in Table 1. - [Example 8] "<Surface layer (A)&gt; The same 4-methyl-1-pentene-based copolymer as in Example 1 was used. <Next layer (B)> Use and Example 1 The same (b)_a, α2_η, and (b2_2) were used as the following resin composition. 9 (bl)-a· 4 methyl-1-pentane-based copolymer 2% by mass. (b2 -l): ethylene/1-butene random copolymer 3 〇 mass%. (b2-2) : 1-butene-ethylene random copolymer 5 enamel 缓冲 <buffer layer (C) &gt; ' Example 2 Similarly, setting (ci)-a to 3 〇% by mass, (c2)-a was 70% by mass, and dry blending was carried out using a Hanschel mixer. <Manufacturing of laminated body> Using three kinds of five-layer T-die devices, the set temperature of the extruder and Τ1•Mold set temperature is set to 290X:, by coextrusion manufacturing by surface layer (A) / «connector layer (B) / buffer layer (C) / connector layer (B) / surface layer (a A wide 400mm laminate made up of 5 layers. The thickness constitution of the obtained laminate and the evaluation results of the respective properties and properties are shown in Table 1-2. Further, in the same manner as in the first embodiment, the single layer films of the adhesive layer (B) and the buffer layer (c) were separately molded to measure MFR1. The results are shown in Table 1__2. [Example 9] <Surface layer (A)&gt; 312XP/Inventive specification (supplement)/95_〇9/95116834 39 1294351 The same 4-meridyl group as the example <adhesion layer (B) &gt; A pentoene-based copolymer. (b2 to 1) and (b2-2), using the same composition ratio as the following (bl)-a in the same manner as in Example 1, the content of the terpene resin composition (bl)-a : 4-mercapto-1 - pentene-based copolymer mass%, MFR2 ··5 g/10 min] 50% by mass. (b2-l)···········································································

(b2-2):卜丁烯•乙烯無規共聚合體[抑^,乙烯含有 量:10 質量 %,MFR1 ·· 0.4g/10 分鐘]4〇 質量 0/〇。 〈緩衝層(C) &gt; ' 與實施例2同樣地,將(c〇 —a設為3〇質量%、(c2) — a 設為70質量%,使用漢歇爾混合器進行乾式摻合。 〈積層體之製造〉 使用3種5層T-模具裝置’將擠出機之設定溫度及τ一 模具之設定溫度設為290 °C,藉共擠出製造由表面層(a)/ 接著層(B)/缓衝層(C)/接著層(B)/表面層(A)之5層所構 成的寬4 0 0丽積層體。將所得之積層體的厚度構成及各物 性值的評價結果示於表1-2。 又,與實施例1同樣地,將接著層(B)及緩衝層(c)之單 層膜分別進行成形,測定MFR1。結果示於表1 — 2。 [實施例10] 〈表面層(A)&gt; 使用與實施例1相同之4-曱基-1-戊烯系共聚合體。 40 312XP/發發明說明書(補件)/95-09/95116834 1294351 〈接著層(B)&gt; 使用與實施例1相同之接著性樹脂組成物。 〈緩衝層(C)&gt; -將與實施例4相同之(cl)-b、(c2)-a及(C2)-b,以與 、實施例4相同之組成比,使用漢歇爾混合器進行乾式摻 合0 〈層(D)&gt; ‘ 單獨使用與實施例4相同之(cl)-b聚醯胺6[三菱工程 _塑膠(股)製,商品名「N〇vamidl〇2〇C」,熔點:218°C,MFR2 : 35g/l〇 分鐘]。 〈積層體之製造〉 使用4種4層T-模具裝置,將擠出機之設定溫度及τ— 模具之設定溫度設為290°C,藉共擠出製造由表面層(Α)/ 接著層(Β)/緩衝層(C)/層(D)之4層所構成的寬4〇〇丽積 層體。將所得之積層體的厚度構成及各物性值的評價結果 不於表1 - 2。 • 又,與實施例1同樣地,將接著層(B)、緩衝層(C)及層 • (D)之單層膜分別進行成形,測定mfri。結果示於表1 — 2。 .[實施例11 ] 將貫施例2所得之積層體表面,以溫度130°C之加熱壓 花泰b進行壓祀處理,得到面粗度Ry為1 〇 μ m的積層體。 所得積層體之加熱及加壓處理前的接著強度為 5· 2N/15mm、加熱及加壓處理後的接著強度為2. 3N/15mm, 超出量為2mm,緩衝量為600 /z m。 312XP/發發明說明書(補件)/95·〇9/95丨丨6834 41 1294351 [比較例1] 〈表面層(A)&gt; 使用與實施例1相同之扣 〈接著層(B)&gt; &quot;戊烯系共聚合體。 使用與實施例1相同之接著性樹脂組成物。 〈緩衝層(c)&gt; w 二)二作為溶點19rc以上之耐熱性樹脂,使 &amp;例i相同之基+戊烯系共聚合體7G質量%。 (c2)-a:作為熔點17代以下之軟質樹脂,使用與 例1相同之低密度聚乙烯30質量%。 其次,將上述(cl)-a及(c2)_a使用漢歇爾混合器 乾式換合。 〈積層體之製造〉 使用3種5層T-模具裝置,將擠出機之設定溫度及τ_ 模具之設定溫度設為29(rc,藉共擠出製造由表面層(α)/ 接著層(Β)/緩衝層(C)/接著層(Β)/表面層(4)之5層所構 •成的寬400mm積層體。將所得之積層體的厚度構成及各物 性值的評價結果示於表2-1。 . 又,與實施例1同樣地,將接著層(B )及緩衝層(C )之單 - 層膜分別進行成形,測定MFR1。結果示於表2-1。 ,[比較例2] 〈表面層(A)&gt; 使用與實施例1相同之4 -甲基-1 -戊烯系共聚合體。 〈接著層(B)&gt; 312XP/發發明說明書(補件y95-09/95116834 42 1294351 使用與實施例1相同之接著性樹脂組成物。 〈缓衝層(c)&gt; (cU-a :作為溶點19(rc以上之耐熱性樹脂,使用與 &quot;施例1相同之4一甲基-1-戊烯系共聚合體60質量%。 -、(c2)_a:作為熔點not以下之軟質樹脂,使用與實於 例1相同之低密度聚乙烯40質量%。 也 其次,將上述(cl)-a及(c2)_a使用漢歇爾混合器 _ 乾式摻合。 參〈積層體之製造〉 使用3種5層T-模具裝置,將擠出機之設定溫度及τ— 模具之設定溫度設為290〇C,藉共擠出製造由表面層(A)/ 接著層(B)/緩衝層(C)/接著層(B)/表面層(^之5層所構 成的寬400mm積層體。將所得之積層體的厚度構成及各物 性值的評價結果示於表2 -1。 又,與實施例1同樣地,將接著層(B)及緩衝層(c)之單 層膜分別進行成形,測定MFR1。結果示於表2d。 春[比較例3] .〈表面層(A)&gt; ,使用與實施例1相同之4-曱基-1-戊烯系共聚合體。 ,〈接著層(B)&gt; 使用與實施例1相同之接著性樹脂組成物。 〈緩衝層(C)&gt; (cl)-a :作為熔點190°C以上之耐熱性樹脂,使用與實 施例1相同之4-曱基-1-戊烯系共聚合體5質量〇/〇。 312χΡ/發發明說明書(補件)/95-09/95116834 43 1294351 (c2)-a ·作為炫點170°C以下之軟質樹脂,使用與實施 例1相同之低密度聚乙烯9 5質量%。 其次,將上述(cl)-a及(c2)-a使用漢歇爾混合器進行 Λ 乾式摻合。 ,〈積層體之製造〉 使用3種5層Τ-模具裝置,將擠出機之設定溫度及丁一 模具之設定溫度設為290°C,藉共擠出製造由表面層(Α)〆 •接著層(B)/緩衝層(C)/接著層(B)/表面層(A)之5層所構 _成的寬400mm積層體。將所得之積層體的厚度構成及各物 性值的評價結果示於表2-1。 又,與貫施例1同樣地’將接著層(B)及緩衝層(c)之單 層膜分別進行成形,測定MFR1。結果示於表π。 [比較例4] 〈表面層(A)&gt; 使用與實施例1相同之4-曱基-1-戊烯系共聚合體。 〈接著層(B)&gt; Φ 使用與實施例1相同之接著性樹脂組成物。 .〈緩衝層(〇&gt; (c2) - a ·作為溶點170 °C以下之軟質樹脂,僅使用與實 . 施例1相同之低密度聚乙烯。 〈積層體之製造〉 使用3種5層T-模具裝置,將擠出機之設定溫度及τ-模具之設定溫度設為290°C,藉共擠出製造由表面層(a)/ 接者層(B)/緩衝層(C)/接者層(B)/表面層(a)之5層所構 312XP/發發明說明書(補件)/95-09/95116834 44 1294351 成的寬40〇mm積層體。將所得之積層體的厚度構成及各物 性值的評價結果示於表2-1。 又’與實施例1同樣地,將接著層(…及緩衝層(c)之單 '層膜分別進行成形,測定MFR1。結果示於表2-1。 '‘[比較例5 ] 〈表面層(A)&gt; 使用與實施例1相同之4-曱基_1-戊烯系共聚合體。 .〈接著層(B)&gt; Φ (Μ) ·作為接著層(B)之樹脂,使用乙烯•丙烯橡膠 [MFR · 2g/l〇分鐘(三井化學(股)製,商品名「三井Ερτ 4021」)]。 〈緩衝層(C) &gt; (c2)-a :作為熔點170。〇以下之軟質樹脂,僅使用與實 施例1相同之低密度聚乙烯。 〈積層體之製造〉 使用3種5層T-模具裝置,將擠出機之設定溫度及丁一 •模具之設定溫度設為290°C,藉共擠出製造由表面層(A)/ •接著層(B)/緩衝層(C)/接著層(B)/表面層(A)之5層所構 . 成的寬400_積層體。將所得之積層體的厚度構成及各物 • 性值的評價結果示於表2 -1。 - 又,與實施例1同樣地,將接著層(B)及緩衝層(C)之單 層膜分別進行成形,測定MFR1。結果示於表2-1。 [比較例6 ] 〈表面層(A)&gt; 312XP/發發明說明書(補件)/95-09/95116834 45 1294351 使用與實施例1相同之4-曱基- 1 -戊稀系共聚合體。 〈接著層(B)&gt; 未使用接著層(B)。 、〈緩衝層(C)&gt; - 與貫施例2同樣地’將(cl)-a設為30質量%、(c2) - a 設為70質量%,使用漢歇爾混合器進行乾式摻合。 〈積層體之製造〉 _ 使用3種5層T-板具裝置’將擠出機之設定溫度及τ 一 _模具之設定溫度設為290X:,藉共擠出製造由表面1(A)/ 緩衝層(C)/表面層(A)之3層所構成的寬4〇〇mm積層體。 將所得之積層體的厚度構成及各物性值的評價結果示於 表2-1。 … ”、 又,與實施例1同樣地,將接著層(“及緩衝層(c)之單 層膜分別進行成形,測定MFR1。結果示於表2 — 1。 [比較例7] 〈表面層(A)&gt;(b2-2): a butene/ethylene random copolymer [suppressed, ethylene content: 10% by mass, MFR1 ··0.4g/10 minutes] 4 〇 mass 0/〇. <Cushion layer (C) &gt; ' In the same manner as in Example 2, (c〇-a was set to 3 〇 mass%, and (c2) - a was set to 70 mass%, and dry blending was performed using a Hanschel mixer. <Manufacturing of laminated body> Using three kinds of five-layer T-die devices', the set temperature of the extruder and the set temperature of the τ-die are set to 290 °C, and the surface layer (a)/ a wide layer of 50 layers formed of five layers of layer (B) / buffer layer (C) / adhesion layer (B) / surface layer (A). The thickness of the resulting laminate is composed of various physical properties. The evaluation results are shown in Table 1-2. Further, in the same manner as in Example 1, the single layer films of the adhesive layer (B) and the buffer layer (c) were each molded, and MFR1 was measured. The results are shown in Table 1-2. Example 10] <Surface layer (A)&gt; The same 4-mercapto-1-pentene copolymer was used as in Example 1. 40 312XP/Invention specification (supplement)/95-09/95116834 1294351 Next, the layer (B) &gt; used the same adhesive resin composition as in Example 1. <Buffer layer (C)> - The same (cl)-b, (c2)-a and (C2) as in Example 4 )-b, the same as in the fourth embodiment The composition ratio was dry blended using a Hanschel mixer. 0 <layer (D)> 'The same (cl)-b polyamide 6 was used as in Example 4 [Mitsubishi Engineering_Plastic (stock) system, commodity "N〇vamidl〇2〇C", melting point: 218 ° C, MFR 2 : 35 g / l 〇 min]. <Manufacture of laminates> Using four 4-layer T-die devices, the set temperature of the extruder and τ—The set temperature of the mold is set to 290 ° C, and the width of the surface layer (Α) / the subsequent layer (Β) / the buffer layer (C) / layer (D) is 4 by the co-extrusion. The thickness of the obtained laminate and the evaluation results of the physical property values are not in Table 1-2. • In the same manner as in the first embodiment, the adhesive layer (B), the buffer layer (C), and the layer are provided. • The single layer film of (D) was separately molded and measured by mfri. The results are shown in Table 1-2. [Example 11] The surface of the laminate obtained in Example 2 was heated at a temperature of 130 ° C. b is subjected to compression treatment to obtain a laminate having a surface roughness Ry of 1 μm. The subsequent strength before the heating and pressure treatment of the obtained laminate is 5·2 N/15 mm, and after heating and pressurization The intensity is 2. 3N/15mm, the excess is 2mm, and the buffer amount is 600 /zm. 312XP/Inventive Manual (Supplement)/95·〇9/95丨丨6834 41 1294351 [Comparative Example 1] <surface layer (A) &gt; The same layer as the first embodiment (the following layer (B) &gt;&quot; pentene copolymer was used. The same adhesive resin composition as in Example 1 was used. <Buffer layer (c)&gt; w 2) The heat-resistant resin having a melting point of 19 rc or more, 7 g mass % of the base + pentene copolymer which is the same as & (c2)-a: As a soft resin having a melting point of 17 or less, 30% by mass of the low-density polyethylene similar to that of Example 1 was used. Next, the above (cl)-a and (c2)_a were dry-fitted using a Hanschel mixer. <Manufacturing of laminated body> Using three kinds of five-layer T-die devices, the set temperature of the extruder and the set temperature of the τ_mold were set to 29 (rc, manufactured by co-extrusion from the surface layer (α) / subsequent layer ( Β) / buffer layer (C) / layer (Β) / surface layer (4) of the five layers of the width of the 400mm layered body. The thickness of the resulting layered structure and the evaluation of the physical properties are shown in Further, in the same manner as in Example 1, the single-layer films of the adhesive layer (B) and the buffer layer (C) were each molded, and MFR1 was measured. The results are shown in Table 2-1. Example 2] <Surface layer (A)&gt; The same 4-methyl-1-pentene-based copolymer as in Example 1 was used. <Next layer (B)> 312XP/Inventive specification (supplement y95-09 /95116834 42 1294351 The same adhesive resin composition as in Example 1 was used. <Buffer layer (c)> (cU-a: as a melting point 19 (heat resistant resin of rc or higher, used and &quot;Example 1 60% by mass of the same 4-methyl-1-pentene copolymer. -, (c2)_a: 40% by mass of the low-density polyethylene similar to that of Example 1 was used as the soft resin having a melting point not or less.Next, the above (cl)-a and (c2)_a are blended using a Hanschel mixer _ dry. Manufacture of the laminated body. Using three kinds of five-layer T-die devices, the set temperature of the extruder and τ—The set temperature of the mold is set to 290 〇C, and the surface layer (A) / the subsequent layer (B) / the buffer layer (C) / the subsequent layer (B) / the surface layer (5 layers of the surface layer) are manufactured by co-extrusion. The thickness of the laminate having a width of 400 mm is shown in Table 2-1. The thickness of the obtained laminate and the evaluation results of the physical properties are shown in Table 2-1. Further, in the same manner as in the first embodiment, the adhesive layer (B) and the buffer layer (c) are used. The monolayer film was separately molded and the MFR1 was measured. The results are shown in Table 2d. Spring [Comparative Example 3] < Surface layer (A)&gt; The same 4-mercapto-1-pentene system as in Example 1 was used. The following is the same as the adhesive resin composition of the first embodiment. <Buffer layer (C)> (cl)-a: a heat-resistant resin having a melting point of 190 ° C or higher, The same 4-mercapto-1-pentene copolymer was used in the same manner as in Example 1. 5 〇/〇. 312χΡ/发发明说明(补件)/95-09/95116834 43 1294351 (c2)-a Point below 170 ° C For the soft resin, the same low-density polyethylene as in Example 1 was used at 95% by mass. Next, the above (cl)-a and (c2)-a were dry blended using a Hanschel mixer. Manufacture > Using three kinds of 5-layer Τ-die devices, the set temperature of the extruder and the set temperature of the Dingyi mold are set to 290 ° C, and the surface layer (Α) 接着 • the subsequent layer (B) is produced by co-extrusion. / / buffer layer (C) / layer (B) / surface layer (A) of the five layers of the structure of the width of 400mm layered body. The thickness constitution of the obtained laminate and the evaluation results of the respective physical properties are shown in Table 2-1. Further, in the same manner as in Example 1, the single layer films of the adhesive layer (B) and the buffer layer (c) were separately molded, and MFR1 was measured. The results are shown in Table π. [Comparative Example 4] <Surface layer (A)&gt; The same 4-mercapto-1-pentene copolymer was used as in Example 1. <Adhesion layer (B)&gt; Φ The same adhesive resin composition as in Example 1 was used. <Buffer layer (〇> (c2) - a · As a soft resin having a melting point of 170 ° C or less, only the same low-density polyethylene as in Example 1 is used. <Manufacture of laminated body> Three types of 5 are used. Layer T-die device, set the temperature of the extruder and the set temperature of the τ-mold to 290 ° C, and manufacture by surface extrusion (a) / connector layer (B) / buffer layer (C) /layer layer (B) / surface layer (a) 5 layer structure 312XP / invention description (supplement) / 95-09/95116834 44 1294351 into a width of 40 〇 mm laminate. The resulting laminate The evaluation results of the thickness configuration and the physical property values are shown in Table 2-1. In the same manner as in Example 1, the single layer films of the adhesive layer (... and the buffer layer (c) were separately molded, and MFR1 was measured. In Table 2-1. ''[Comparative Example 5] <Surface layer (A)&gt; The same 4-mercapto-1-pentene-based copolymer as in Example 1 was used. <Sublayer (B)&gt; Φ (Μ) · As the resin of the adhesive layer (B), ethylene/propylene rubber is used [MFR · 2g/l〇 minutes (Mitsui Chemical Co., Ltd., trade name "Mitsui Ερτ 4021"). ) &gt; (c2)-a : as For the soft resin having a melting point of 170 〇, only the same low-density polyethylene as in Example 1 was used. <Manufacture of laminate> Three sets of 5-layer T-die devices were used to set the temperature of the extruder and the mold The set temperature was set to 290 ° C, and the five layers of the surface layer (A) / • the subsequent layer (B) / the buffer layer (C) / the subsequent layer (B) / the surface layer (A) were fabricated by co-extrusion. The width of the laminate is 400. The thickness of the obtained laminate and the evaluation results of the properties are shown in Table 2-1. - In the same manner as in the first embodiment, the adhesive layer (B) and The single layer film of the buffer layer (C) was separately molded, and MFR1 was measured. The results are shown in Table 2-1. [Comparative Example 6] <Surface layer (A)&gt; 312XP/Inventive specification (supplement)/95-09 /95116834 45 1294351 The same 4-mercapto-1 -pentane-based copolymer as in Example 1 was used. <Sublayer (B)&gt; The adhesive layer (B) was not used. <Buffer layer (C)&gt; In the same manner as in Example 2, 'cl)-a was 30% by mass, and (c2) - a was 70% by mass, and dry blending was carried out using a Hanschel mixer. <Manufacture of laminated body> _ Use 3 types of 5 layers The T-plate device 'sets the set temperature of the extruder and the set temperature of the τ__mold to 290X: by surface extrusion 1 (A) / buffer layer (C) / surface layer (A) The thickness of the multilayer structure of the three layers was set as follows. The thickness of the obtained laminated body and the evaluation results of the physical property values are shown in Table 2-1. Further, in the same manner as in Example 1, the single layer film of the adhesive layer ("and the buffer layer (c) was separately molded, and MFR1 was measured. The results are shown in Table 2-1. [Comparative Example 7] <Surface layer (A)&gt;

使用與實施例1相同之4-曱基—1-戊婦系 〈接著層(B)&gt; ^ 共聚合體。 未使用接著層(B)。 〈緩衝層(C)&gt; (cl)-a:作為熔點190。。以上之耐熱性樹脂,使 施例&quot;目同之4-甲基+戊稀系共聚合體3〇質量 (加作為溶,點170。。以下之敕質樹脂,使 例1相同之低密度聚乙烯50質量%。 /、Μ 312ΧΡ/發發明說明書(補件)/9谓951!觀 46 1294351 (c2)-e :使用丙烯之無規共聚合體[熔點:138。[,MFRi : 7.〇g/10分鐘(三井化學(股)製,商品名「三井p〇lypr〇 F327」)]20 質量 %。 、 其次,將上述(cl)-a、(c2)-a及(c2)-e使用漢歇爾混 • 合器進行乾式摻合。 〈積層體之製造〉 使用3種5層T-模具裝置,將擠出機之設定溫度及τ一 •模具之設定溫度設為290°C,藉共擠出製造由表面層(A)/ 擎緩衝層(C)/表面層(A)之3層所構成的寬4〇〇mm積層體。 將所得之積層體的厚度構成及各物性值的評價結果示於 表 2 -1 〇 又,與實施例1同樣地,將接著層〇)及緩衝層(C)之單 層膜分別進行成形,測定MFR1。結果示於表。 [比較例8 ] 〈表面層(A)&gt; 使用與實施例 _ &lt;接著層(B)&gt; 相同之4-甲基-1-戊烯系 共聚合體。 、使用與實施例1相同之⑽-a、(bM)、(b2_2),使用 以下組成比之接著性樹脂組成物。 (bl)-a : 4-曱基-1-戊烯系共聚合體1〇質量%。 (b2-l):乙烯•卜丁烯無規共聚合體4〇質量%。 (b2-2):卜丁烯•乙烯無規共聚合體5〇 〈緩衝層(C)&gt; ' 與實施例2同樣地,將(cl)_a設為 30質量% (。2)-a 312XP/發發明說明書(補件)/95-09/95116834 47 1294351 設為70質量%,使用漢歇爾混合器進行乾式摻合。 〈積層體之製造〉 使用3種5層T-模具裝置,將擠出機之設定溫度及τι 模具之設定溫度設為290°C,藉共擠出製造由表面^(Α)/ 、接著層(B)/緩衝層(C)/接著層(B)/表面層(A)之5 ^所構 成的寬400mm積層體。將所得之積層體的厚度構成及各物 性值的評價結果示於表2-1。 又,與實施例1同樣地,將接著層(B)及緩衝層(c)之單 _層膜分別進行成形,測定MFR1。結果示於表24。 [比較例9 ] 〈表面層(A)&gt; 使用與實施例1相同之4-甲基-1-戊烯系共聚合體。 〈接著層(B)&gt; 使用與實施例1相同之(b〇-a、α2_υ、(b2_2),使用 以下組成比之接著性樹脂組成物。 (bl)-a : 4-甲基-1-戊烯系共聚合體2〇質量%。 • (b2 —丨):乙烯·卜丁烯無規共聚合體5〇質量〇/〇。 • (b2 —2) ··卜丁烯•乙烯無規共聚合體3〇質量%。 〈緩衝層(C)&gt; ' .與實施例2同樣地,將(cl)-a設為3〇質量%、(c2)—a -設為70質量%,使用漢歇爾混合器進行乾式摻合。 〈積層體之製造〉 / 使用3種5層Τ-模具裝置,將擠出機之設定溫度及τ_ 模具之設定溫度設為29(rc,藉共擠出製造由表面層(α)/ 312ΧΡ/發發明說明書(補件)/95-09/95116834 48 1294351 接著層(B)/緩衝層(C)/接著層(B)/表面層(幻之5層所構 成的寬40〇mm積層體。將所得之積層體的厚度構成及各物 性值的評價結果示於表2 —2。 、 又’與實施例1同樣地,將接著層(B)及緩衝層(C)之單 ^層膜分別進行成形,測定MFR1。結果示於表2-2。 [比較例10] 〈表面層(A)&gt; . 使用與實施例1相同之4-曱基-1-戊烯系共聚合體。 •〈接著層(B)&gt; 使用與實施例1相同之(bl) —a、(b2 —υ、(b2 —2),使用 以下組成比之接著性樹脂組成物。 (bl)-a : 4-曱基-1-戊烯系共聚合體4〇質量%。 (b2-1) ··乙烯· 1-丁浠無規共聚合體35質量%。 (b2-2): 1-丁烯•乙烯無規共聚合體25質量%。 〈緩衝層(C)&gt; 與實施例2同樣地,將(ci) —a設為3〇質量%、(c2) — a #設為7 0質量%,使用漢歇爾混合器進行乾式摻合。 〈積層體之製造〉 • 使用3種5層T-模具裝置,將擠出機之設定溫度及τ-模具之設定溫度設為290°C,藉共擠出製造由表面層(a)/ .接著層(B)/緩衝層(C)/接著層(B)/表面層(A)之5層所構 成的寬400mm積層體。將所得之積層體的厚度構成及各物 性值的評價結果示於表2-2。 又,與實施例1同樣地,將接著層(B)及緩衝層(c)之單The same 4-mercapto-l-pentanose <adhesion layer (B) &gt; ^ copolymer was used as in Example 1. The subsequent layer (B) is not used. <Buffer layer (C)&gt; (cl)-a: As melting point 190. . The above heat-resistant resin was subjected to the same method as the 4-methyl + pentane copolymer 3 〇 mass (added as a solvent, point 170. The following enamel resin, the same low density of the same as in Example 1 Ethylene 50% by mass. /, Μ 312 ΧΡ / issued invention specification (supplement) / 9 said 951! View 46 1294351 (c2)-e: using a random copolymer of propylene [melting point: 138. [, MFRi: 7.〇 g/10 minutes (Mitsui Chemical Co., Ltd., trade name "Mitsui p〇lypr〇F327")] 20% by mass. Next, the above (cl)-a, (c2)-a and (c2)-e Dry blending using a Hanschel mixer. <Manufacturing of laminated body> Using three 5-layer T-die devices, the set temperature of the extruder and the set temperature of the τ-die are set to 290 °C. A wide 4 mm thick laminate composed of three layers of the surface layer (A) / the buffer layer (C) / the surface layer (A) is produced by co-extrusion. The thickness of the obtained laminate is composed and the physical properties are obtained. The evaluation results are shown in Table 2-1. Further, in the same manner as in Example 1, the single layer films of the underlayer layer and the buffer layer (C) were separately molded, and MFR1 was measured. The results are shown in the table. [Comparative Example 8] <Surface layer (A)&gt; A 4-methyl-1-pentene copolymer was used in the same manner as in Example _ &lt;Layer layer (B)&gt;. Using the same (10)-a, (bM), and (b2_2) as in Example 1, the following composition ratio of the adhesive resin composition was used. (bl)-a : 4-mercapto-1-pentene copolymer of 1% by mass. (b2-l): ethylene/b-butene random copolymer 4% by mass. (b2-2): Butene/ethylene random copolymer 5 〇 <Buffer layer (C)> ' In the same manner as in Example 2, (cl)_a was set to 30% by mass (.2)-a 312XP / Inventive Manual (Supplement) / 95-09/95116834 47 1294351 Set to 70% by mass, dry blending using a Hanschel mixer. <Manufacturing of laminated body> Using three kinds of five-layer T-die devices, the set temperature of the extruder and the set temperature of the mold are set to 290 ° C, and the surface is manufactured by extrusion ( ) / / layer (B) / Buffer layer (C) / Adhesion layer (B) / Surface layer (A) 5 ^ wide 400mm laminate. The thickness constitution of the obtained laminate and the evaluation results of the respective physical properties are shown in Table 2-1. Further, in the same manner as in Example 1, the single layer films of the adhesive layer (B) and the buffer layer (c) were each molded, and MFR1 was measured. The results are shown in Table 24. [Comparative Example 9] <Surface layer (A)&gt; The same 4-methyl-1-pentene copolymer was used as in Example 1. <Adhesive layer (B)&gt; The same adhesive composition as the following composition ratio was used in the same manner as in Example 1 (b〇-a, α2_υ, (b2_2). (bl)-a : 4-methyl-1 - pentene-based copolymer 2% by mass. • (b2 - 丨): ethylene-b-butene random copolymer 5 〇 mass 〇 / 〇. (b2 - 2) · · Butene - ethylene random copolymerization In the same manner as in the second embodiment, (cl)-a is set to 3% by mass, and (c2)-a is set to 70% by mass. Dry blending by the Michelle mixer. <Manufacturing of laminated body> / Using three kinds of 5-layer Τ-die devices, the set temperature of the extruder and the set temperature of τ_ mold are set to 29 (rc, manufactured by co-extrusion) From the surface layer (α) / 312 ΧΡ / issued invention instructions (supplement) / 95-09/95116834 48 1294351 then layer (B) / buffer layer (C) / layer (B) / surface layer (magic 5 layer The thickness of the laminated body is 40 mm. The thickness of the obtained laminated body and the evaluation results of the respective physical properties are shown in Table 2-1. In the same manner as in the first embodiment, the adhesive layer (B) and the buffer layer are provided. (C) single layer film Molding was carried out, and MFR1 was measured. The results are shown in Table 2-2. [Comparative Example 10] <Surface layer (A)&gt; The same 4-mercapto-1-pentene copolymer was used as in Example 1. <Adhesive layer (B)&gt; The same (b)-a: 4 was used as in the case of (b1)-a, (b2 - υ, (b2 - 2), and the following composition ratio was used. - mercapto-1-pentene copolymer 4 〇% by mass. (b2-1) ······························ In the same manner as in the second embodiment, (ci) - a is set to 3 % by mass, and (c2) - a # is set to 70% by mass. Dry mixing by the Michelle mixer. <Manufacturing of laminated body> • Using three 5-layer T-die devices, the set temperature of the extruder and the set temperature of the τ-die are set to 290 ° C. A 400 mm wide laminate consisting of 5 layers of surface layer (a) / .sublayer layer (B) / buffer layer (C) / adhesion layer (B) / surface layer (A) is produced. The thickness of the resulting laminate is obtained. The evaluation results of the composition and the physical property values are shown in Table 2-2. Single the same manner as in Example, the adhesive layer 1 (B) and the buffer layer (c) of the Embodiment

312XP/發發明說明書(補件)/95-09/95116834 49 1294351 層膜分別進行成形,測定MFRl。結果示於表2_2。 [比較例11 ] 〈表面層(A)&gt; ;使用與實施例1相同之4-甲基+戊烯系共聚合體。 1 〈接著層(B)&gt; 使用與實施例1相同之(bl)_a、α2_υ、(b2_2),使用 以下組成比之接著性樹脂組成物。 - (bl) 一a : 4一曱基―1 —戊烯系共聚合體6〇質量%。 • (b2-D :乙烯·卜丁烯無規共聚合體5質量%。 (b2-2) : 1-丁烯•乙烯無規共聚合體35 〈緩衝層(〇&gt; ' 與貫施例2同樣地,將(ci )—a設為3〇質量%、(c2)—a 设為7 0質篁% ’使用漢歇爾混合器進行乾式摻合。 〈積層體之製造〉 使用3種5層T-模具裝置,將擠出機之設定溫度及τ— 模具之設定溫度設為290°C,藉共擠出製造由表面層(a)/ •接著層(B)/緩衝層(C)/接著層(B)/表面層(A)之5層所構 成的寬400mm積層體。將所得之積層體的厚度構成及各物 性值的評價結果示於表2-2。 , 又,與實施例1同樣地,將接著層(B)及緩衝層(c)之單 • 層膜分別進行成形,測定MFR1。結果示於表2-2。 [比較例12] 〈表面層(A)&gt; 使用與實施例1相同之4-曱基-1 -戊烯系共聚合體。 50 312XP/發發明說明書(補件)/95-09/95116834 1294351 〈接著層(B)&gt; 使用與實施例1相同之(bl)-a、α2-1)、(b2_2),使用 以下組成比之接著性樹脂組成物。 (bl)-a : 4-甲基-1-戊烯系共聚合體25質量%。 (b2-l) ·乙稀· 1 —丁烯無規共聚合體5質量%。 (b2-2) · 1- 丁烯•乙浠無規共聚合體質量%。 〈緩衝層(C)&gt; - 與貫施例2同樣地,將(cl)-a設為30質量%、(c2)-a 春設為70質量%,使用漢歇爾混合器進行乾式摻合。 〈積層體之製造〉 使用3種5層T-模具裝置,將擠出機之設定溫度及τ一 模具之設定溫度設為29(TC,藉共擠出製造由表面層(A)/ 接著層(B)/緩衝層(C)/接著層(B)/表面層(a)2 5層所構 成的寬400顏積層體。將所得之積層體的厚度構成及各物 性值的評價結果示於表2 — 2。 又,與實施例1同樣地,將接著層(]8)及緩衝層(c)之單 •層膜分別進行成形,測定MFRl。結果示於表2 —2。 .[比較例13] 〈表面層(A)&gt; 使用與實施例 〈接著層(B)&gt; 1相同之4-甲基-1-戊烯系共聚合體。 量 (bl)—b : 4一曱基一丨―戊烯系共聚合體[1-癸烯含有 312XP/發發明說明書(補件)/95·〇9/95116834 51 1294351 質量%,、溶點:222 °C、MFR2 : 250g/i〇分鐘,密度: 835kg/m3(ASTM D1 505)]35 質量%。 (b2-l):乙烯· 1-丁烯無規共聚合體15質量%。 u (b2_2) · 1-丁細•乙烯無規共聚合體質量%。 ;〈缓衝層(C)&gt; 與實施例2同樣地,將(ci)-a設為3〇質量%、(^)一&amp; 設為70質量%,使用漢歇爾混合器進行乾式掺合。 〈積層體之製造〉 鲁#使用3種5層T-模具裝置,將擠出機之設定溫度及τ_ 模具之設定溫度設為290〇C,藉共擠出製造由表面層(Α)/ 接著層⑻/緩衝層(C)/接著層⑻/表面層⑴之“所構 成的寬4_m積層冑。將所得之積層體的厚度構成及各物 性值的評價結果示於表2-2。 又,與實施例1同樣地,將接著層(B)及緩衝層(C)之單 層膜分別進行成形,測定MFR、結果示於表2_2。 [比較例14 ] Φ〈表面層(A)&gt; 使用與實施例1相同之4-甲基+戊婦系共聚合體。 〈接著層(B)&gt; 使用與實施例1相同之接著性樹脂組成物。 〈緩衝層(c)&gt; (:l)-a :作為溶點職以上之耐熱性樹脂,使用與表 4 (A)相同之4-甲基-1-戊烯系共聚合體3〇質量%。 ⑽|作為㈣17代以下之軟質樹脂,使用低密度 312XP/發發明說明書(補件)/95-09/95116834 52 1294351 聚乙烯[熔點:110 °c,MFR1 : 0· 6g/l〇分鐘,密度·· 920kg/m3(ASTM D1505)]70 質量%。 其次,將上述(cl)-a及(c2)-f使用漢歇爾混合器進行 ' 乾式摻合。 \ 〈積層體之製造〉 使用3種5層T-模具裝置,將擠出機之設定溫度及τ— 模具之設定溫度設為290°C,藉共擠出製造由表面層(a)/ 接者層(B)/緩衝層(C) /接著層(B) /表面層(a)之5層所構 春成的寬400mm積層體。將所得之積層體的厚度構成及各物 性值的評價結果示於表2-2。 又,與實施例1同樣地,將接著層(B)及緩衝層(c)之單 層膜分別進行成形,測定MFR1。結果示於表2-2。 [比較例15] 〈表面層(A)&gt; 使用與實施例1相同之4-曱基-1 —戊烯系共聚合體。 〈接著層(B)&gt; • 使用與實施例1相同之接著性樹脂組成物。 •〈緩衝層(C)&gt; - (Cl)-a:作為熔點190°C以上之耐熱性樹脂,使用與表 r面層(A)相同之4_甲基―丨一戊烯系共聚合體30質量%。 (c2)-g:作為熔點17(TC以下之軟質樹脂’使用低密度 聚乙烯[熔點:11(TC,MFR1 : 30g/1〇分鐘,密度: 920kg/m3(ASTM D1 505)]70 質量 %。 其次,將上述(cl)-a及(c2)—g使用漢歇爾混合器進行 312XP/發發明說明書(補件)/95-09/95116834 53 1294351 乾式摻合。 〈積層體之製造〉 使用3種5層T-模具裝置,將擠出機之設定溫度及T-\ 模具之設定溫度設為290°C,藉共擠出製造由表面層(A)/ ' 接著層(B)/緩衝層(C)/接著層(B)/表面層(A)之5層所構 成的寬400mm積層體。將所得之積層體的厚度構成及各物 性值的評價結果示於表2-2。 . 又,與實施例1同樣地,將接著層(B)及緩衝層(C)之單 φ層膜分別進行成形,測定MFR1。結果示於表2-2。312XP/Inventive Manual (Supplement)/95-09/95116834 49 1294351 The film was separately formed and the MFR1 was measured. The results are shown in Table 2_2. [Comparative Example 11] <surface layer (A)&gt;; The same 4-methyl+pentene copolymer as in Example 1 was used. 1 <Adhesion layer (B)&gt; The same composition ratio of the following composition (b)_a, α2_υ, (b2_2) was used, and the following composition ratio was used. - (bl) One a : 4 - fluorenyl - 1 - pentene copolymer 6 〇 mass %. (b2-D: ethylene-b-butene random copolymer 5 mass%. (b2-2): 1-butene/ethylene random copolymer 35 <buffer layer (〇&gt; ' Same as Example 2 Ground, (ci)-a is set to 3〇% by mass, and (c2)-a is set to 70% by mass%. 'The Hansler mixer is used for dry blending. <Layer manufacturing> Three types of 5 layers are used. T-die device, set the extruder set temperature and τ-mold set temperature to 290 ° C, by co-extrusion manufacturing from surface layer (a) / • adhesion layer (B) / buffer layer (C) / Next, a layered body having a width of 400 mm composed of five layers of the layer (B)/surface layer (A) is shown in Table 2-2, and the results of evaluation of the thickness of the obtained layered product and the respective physical property values are shown in Table 2-2. In the same manner, the single layer films of the adhesive layer (B) and the buffer layer (c) were separately molded, and MFR1 was measured. The results are shown in Table 2-2. [Comparative Example 12] <Surface layer (A)> Use The same 4-mercapto-1 -pentene-based copolymer as in Example 1. 50 312XP/Inventive Specification (Supplement)/95-09/95116834 1294351 <Bottom Layer (B)> Use the same as Example 1. (bl)-a, α2-1), (b2_ 2) The following composition ratio is used as the adhesive resin composition. (bl)-a : 4-methyl-1-pentene-based copolymer 25 mass%. (b2-l) · ethylene · 1-butene (b2-2) · 1-butene-acetamethylene random copolymer mass%. <Buffer layer (C)> - In the same manner as in Example 2, (cl)-a 30% by mass, (c2)-a, and 70% by mass in spring, and dry blending using a Hanschel mixer. <Manufacturing of laminated body> Using three kinds of 5-layer T-die devices, the extruder was used. The set temperature and the set temperature of the τ-die are set to 29 (TC, manufactured by co-extrusion from the surface layer (A) / the subsequent layer (B) / the buffer layer (C) / the subsequent layer (B) / the surface layer (a) A wide-width 400-layer laminate composed of two layers, and the thickness of the obtained laminate and the evaluation results of the physical property values are shown in Table 2-1. Further, in the same manner as in the first embodiment, the adhesive layer (8) was used. The single layer film of the buffer layer (c) was separately molded, and MFR1 was measured. The results are shown in Table 2-1. [Comparative Example 13] <Surface layer (A)> Use and Example <Bottom layer (B) &gt; 1 identical 4-methyl-1-pentene copolymerization Quantity (bl)-b: 4-mercapto-one-pentene-based copolymer [1-decene contains 312XP/inventive specification (supplement)/95·〇9/95116834 51 1294351 mass%, soluble Point: 222 ° C, MFR 2 : 250 g / i 〇 minutes, density: 835 kg / m 3 (ASTM D1 505)] 35 mass %. (b2-l): 15% by mass of an ethylene·1-butene random copolymer. u (b2_2) · 1-butyl fine • Ethylene random copolymer mass%. <Cushion Layer (C)> In the same manner as in Example 2, (ci)-a was set to 3% by mass, (^) and &amp;&gt; was set to 70% by mass, and dried using a Hanschel mixer. Blending. <Manufacturing of laminated body> Lu# uses three kinds of five-layer T-die devices, and sets the set temperature of the extruder and the set temperature of the τ_mold to 290 〇C, and manufactures the surface layer (Α)/ The layer (8) / the buffer layer (C) / the subsequent layer (8) / the surface layer (1) "the width of the layer 4 m is 胄. The thickness of the obtained laminate and the evaluation results of the physical properties are shown in Table 2-2. In the same manner as in Example 1, the single layer films of the adhesive layer (B) and the buffer layer (C) were each molded, and MFR was measured, and the results are shown in Table 2-2. [Comparative Example 14] Φ <surface layer (A) &gt; The same 4-methyl+pentanthene copolymer group as in Example 1 was used. <Adhesion layer (B)&gt; The same adhesive resin composition as in Example 1 was used. <Buffer layer (c)&gt; (:l -a : As a heat-resistant resin having a melting point or higher, the 4-methyl-1-pentene copolymer of the same type as in Table 4 (A) is used in an amount of 3% by mass. (10)|As a soft resin of (four) 17th generation or less, Use low density 312XP / invention manual (supplement) / 95-09/95116834 52 1294351 polyethylene [melting point: 110 °c, MFR1: 0 · 6g / l 〇 minutes, density · 920kg / m3 (ASTM D1 505)] 70% by mass. Next, the above (cl)-a and (c2)-f were subjected to 'dry blending using a Hanschel mixer. \ <Manufacture of laminated body> Three kinds of 5-layer T-die devices were used. The set temperature of the extruder and the set temperature of the τ-die are set to 290 ° C, and the surface layer (a) / the carrier layer (B) / the buffer layer (C) / the subsequent layer (B) are manufactured by co-extrusion. / The layer of the 400 mm wide layer of the surface layer (a) is formed in the same manner as in the first embodiment, and the thickness of the obtained layered product and the evaluation results of the respective physical properties are shown in Table 2-2. The single layer films of the next layer (B) and the buffer layer (c) were separately molded, and MFR1 was measured. The results are shown in Table 2-2. [Comparative Example 15] <Surface layer (A)> Use and Example 1 The same 4-mercapto-1-pentene-based copolymer. <Adhesion layer (B)> • The same adhesive resin composition as in Example 1 was used. • <Buffer layer (C)&gt; - (Cl) - a: The heat-resistant resin having a melting point of 190 ° C or higher is 30% by mass of the 4-methyl-non-pentene-based copolymer which is the same as the surface layer (A). (c2)-g: as the melting point 17 (Soft resin below TC' use Low-density polyethylene [melting point: 11 (TC, MFR1: 30 g / 1 min, density: 920 kg/m3 (ASTM D1 505)] 70% by mass. Next, the above (cl)-a and (c2)-g are used. The Hanschel mixer is 312XP/inventive specification (supplement)/95-09/95116834 53 1294351 dry blending. <Manufacturing of laminated body> Using three kinds of five-layer T-die devices, the set temperature of the extruder and the set temperature of the T-\ mold were set to 290 ° C, and the surface layer (A) / ' was produced by co-extrusion. Next, a layer of 400 mm wide consisting of five layers of layer (B) / buffer layer (C) / adhesion layer (B) / surface layer (A). The thickness constitution of the obtained laminate and the evaluation results of the physical property values are shown in Table 2-2. Further, in the same manner as in Example 1, the single φ layer films of the adhesive layer (B) and the buffer layer (C) were each molded, and MFR1 was measured. The results are shown in Table 2-2.

312XP/發發明說明書(補件)/95-09/95116834 54 1294351 (Ts LO (k 4-曱基-1-戊烯系共聚合 體 g ? g X r-jH S f r^H 0.06 35/15/50 Oj W 1' 1 A oo oo 20/60/20 1 1 1 1 1 1 A/B/C/B/A 25/10/50/10/25 cd (NI CO οα s LO 寸 I m 4-曱基-1-戊烯系共聚合 1 體 g ϊ 4 CjJ g Λ ϊ—H s 5 i i 0.06 35/15/50 X Cj eg A\ ϊ—H CO oi 20/60/20 1 1 1 1 1 1 A/B/C/B/A 25/10/50/10/25 οα ιή oo CNi (Nl ◦ S CO 1 ίΚ 4-曱基-卜戊烯系共聚合 體 g i 1 X r-jH &lt;NI f T—&lt; 0.06 35/15/50 (cl)-a/(c2)-a LO ◦· 40/60 1 1 1 1 1 1 A/B/C/B/A 25/10/50/10/25 LO CD CD oi τ—Η o 穿 03 I ik 4-曱基-卜戊烯系共聚合 體 ◦ (bl)-a/(b2-l)/(b2-2) 0.06 35/15/50 (cl)-a/(c2)-a OO 〇· 30/70 1 1 1 1 1 1 A/B/C/B/A 25/10/50/10/25 寸 LO CD oi οα o s 實施例1 4-曱基-1-戊稀系共聚合 體 g i 1 cja g Λ ϊ 1 i s i g c=&gt; 35/15/50 (cl)-a/(c2)-a t-H 20/80 1 1 1 1 1 1 A/B/C/B/A 25/10/50/10/25 OO 寸· οα CD S 〇IBp 1 1 ψ ◦ 質量% 1 1 φ\ &lt;=) 麵c 1 1 Φ\ 茶 ο 1 1 φ\ 茶 ο 白 1 N/15mm 1 N/15mm 画 ε 樹脂種 Ϊ 1 構成 1 I 構成 1 比例 1樹脂種1 δ3 積層體之各層厚度 加熱及加壓處理前之接著強度 加熱及加壓處理後之接著強度 超出量 φ4 表面層(A) 接著層(B) 緩衝層(c) 層(D) s^s^s - X3 9 $SBS4 is f§s?l-iocdAp) (T§ xs s^s^sss^i - xs 9^ifgft4: ◦1(0) ||^鉍沭^墀裝to·裝h-l:Q—zq) 寸 S911s/60iA6/ffiii)_K?iiK餾^ΜΧίΝΐΓη 1294351 (2丨一 &lt;) 實施例10 4-曱基-1-戊烯系共聚合 體 g 1 i (bl)-a/(b2-l)/(b2-2) 0.06 35/15/50 (cl)-b/(c2)-a/(c2)-b CO cvi 20/60/20 (cl)-b CJi g A/B/C/D 25/10/50//25 τ—Η 寸· CO (Ni &lt;NI ο 另 03 I 4-曱基-1-戊烯系共聚合 體 g ι—Η cva 1 ( Λ i—4 i A cr&gt; 〇· 50/10/40 73 § Λ i—H oo ◦· 30/70 1 1 1 1 1 1 VB/C/B/A 25/10/50/10/25 CO LO 卜 CNi r-H ο in 〇〇 ¥ 4-曱基-1-戊烯系共聚合 體 g g A i H ! i &quot; H LO CN1 ◦· 20/30/50 (cl)-a/(c2)-a oo CD 30/70 1 1 1 1 1 1 A/B/C/B/A 25/10/50/10/25 寸 (N1 s CO 實施例7 4-曱基-1_戊烯系共聚合 體 g τ—Η cji g r-jH έ Λ r^H g &lt;〇 35/15/50 (cl)-a/(c2)-d LO r-H 15/85 1 1 1 1 1 1 A/B/C/B/A 25/10/50/10/25 卜 LO 卜 od (NI o CD I 4-曱基-1-戊烯系共聚合 體 g ι—Η Cp H ^N r^H 0.06 35/15/50 (cl)-a/(c2)-c ΟΪ CO 30/70 1 1 1 1 1 1 A/B/C/B/A 25/10/50/10/25 OO ζό LO CO οα C3 g s olnp 1 1 ◦ ♦1 1 1 φ\ l CD s φ| ®DC 1 1 姻 : o 1 1 ψ ◦ 質量% ε 3 -1 N/15mm N/15mm 圍 B 樹脂種 S 比例 構成 I Jj % 比例 樹脂種 I 比例 積層體之各層厚度 加熱及加壓處理前之接 著強度 加熱及加壓處理種:之接 著強度 超出量 表面層(A) 接著層(B) 緩衝層(c) 層⑼ ϋφ鉍沭嚓礫裝hli ·裝ve 韜命鉍沭喊裝v'l_®-—寸 ϋφ龄咪嗦碟裝l·'·裝to 9ln xs o—§ q—(s f§ f(p)Ms (z丨§ (i) Ms 寸 eoo9 IIlr&gt;6/60^6/(t=3i)_s?ss餾餾/dx(NI ε 12943 t嫩列8 L/i 4-甲奸·系微 8 r_— (bl)^/(b2-l)/(b2-2) ο Η 10/40/50 (cl)-a/(c2)-a 〇〇 30/70 WC7B/A 25/10/50/10/25 LO ◦· οα ◦· 寸 g oo (列 7 4-甲奸觸系共聚 8 1 (cl)-a/(c2)-a/(c2H LO 30/50/20 M7A 25/70/25 1 1 1 1 CO CZ) LO (NI 卜_列6 4-甲务1 - 系共聚 g 1_ (cl)-^/(c2)-a 〇〇 CD 30/70 A/C7A 25/70/25 1 1 1 1 却 g 辦删5 4-甲基·1_·系共聚 g g Q (Ni g (c2)-a CM τ·-Η g i i A/M7B/A 25/10/50/10/25 LO ◦· Τ-Η C5 CD § 匕_列4 4-甲H-麟系共聚 S r-H s Λ 1 5 s ◦· 35/15/50 (c2)-a (N1 r—H s T—^ k/WUWK 25/10/50/10/25 m 寸· C3 oi CO s oo thlii列 3 4-甲奸鱗系共聚 g 9 &gt;s i &gt; 0.06 35/15/50 (cl)-a/(c2)-a CD r-H s A/M7B/A 25/10/50/10/25 oo 寸· 1 &lt; oi CO C5 S 蝴2 4-曱基4-觸系共聚 g 1 έ &gt; /^N s 0.06 35/15/50 (cl)-a/(c2)-a &lt;=&gt; 60/40 WC7B/A 25/10/50/10/25 οα 00 τ—Η LO CO r—H t—H s t嫩列1 4-甲H-猶系共聚 ί 總 s 1 έ &gt; /^N S 0.06 35/15/50 (cl)-a/(c2)-a t—H o ◦’ 70/30 A/B/C/B/A 25/10/50/10/25 22.3 卜 卜· r-H s &amp;即 ί S 綠 ! 1 1 ί AH &lt;=&gt; m〇 t N/15mm N/15mm 謹 白 Ϊ 1 ϊ 醤 1 s ΟΛ 1 1 ί 麟歡綠厚度 53 Ϊ t ^ 2 3 超出量 &quot;mm*&quot;&quot;&quot;&quot;&quot; 表&amp;f(A) 接著層⑻ mmco 鍥命鉍爱ν-ιΫ5Η丨寸 1) (i cd丨(lq) Διο 0丨§MsMs 17es9I^6/6s6/ff}«)_s^K^#/dx(NIcn 1294351 (7¾ t嫩歹丨J15 4-甲壯麟系 共聚雜 S r—Η (bl)-a/(b2-l)/(b2-2) s c=&gt; 35/15/50 ! 30/70 ymm 25/10/50/10/25 LO 〇J ① LO § t嫩列14 4-曱基Ί-麟系 共聚緣 S 9 苕 s s ◦· 35/15/50 (cl)-a/(c2)-f CO ◦· 30/70 A/M7B/A 25/10/50/10/25 〇j Cvl CN1 § 罐歹丨J13 4-甲壯麟系 共聚雜 S C£5 &lt;=5 35/15/50 (cl)-a/(c2)-a oo ◦· 30/70 mimik 25/10/50/10/25 LO CO (Νί oo § 瞻列12 4-甲基4-麟系 共聚雜 S r-H (bl&gt;a/(b2-l)/(b^) ◦· 25/5/70 (cl)-a/(c2)-a oo 〇· 30/70 mimik 25/10/50/10/25 CNI C&lt;i CD CO § t麵11 4-甲&amp;4-麟系 共聚徽 s (bl)-a/(b2-l)/(b2-2) |t—H c=&gt; 60/5/35 (cl)-a/(c2&gt;a oo C=) 30/70 rnmik 25/10/50/10/25 LO oi CO CO § 瞻列10 4-曱H-麟系 共聚綠 s 9 1 S Q· 40/35/25 (cl)-a/(c2)-a OO 30/70 25/10/50/10/25 CO § 賴列9 4-甲壯麟系 共聚雜 s l—i 1 1 CO &lt;=&gt;* 20/50/30 (cl)-a/(c2)-a oo ◦· 30/70 mimik 25/10/50/10/25 05 寸 ! % % ! 1 1 ! 1 1 imc t Wldm N/15im 国 t Ϊ 1 1 ΛΧ Ϊ 1 5 1 1 1 顧 輸 4總級 力趨 ΜάΛ s 表®^(A) mm) I I C〇 二 /^、,-Ν I I τ—I &lt;ΝΙ /^Ν Ζ^Ν I I τ—Η τ—· 〇νί CO JD JD Χ5 VS_^ · β—^ 丨一 · s svs^s—3^—^ S^S0^ ssfs s^s w^s4^n^^viii^&amp;-^312XP/Inventive Manual (supplement)/95-09/95116834 54 1294351 (Ts LO (k 4-mercapto-1-pentene copolymer) g ? g X r-jH S fr^H 0.06 35/15/ 50 Oj W 1' 1 A oo oo 20/60/20 1 1 1 1 1 1 A/B/C/B/A 25/10/50/10/25 cd (NI CO οα s LO inch I m 4- Mercapto-1-pentene copolymerization 1 body g ϊ 4 CjJ g Λ ϊ—H s 5 ii 0.06 35/15/50 X Cj eg A\ ϊ—H CO oi 20/60/20 1 1 1 1 1 1 A/B/C/B/A 25/10/50/10/25 οα ιή oo CNi (Nl ◦ S CO 1 Κ 4- 4-yl-p-pentene copolymer gi 1 X r-jH &lt;NI f T—&lt; 0.06 35/15/50 (cl)-a/(c2)-a LO ◦· 40/60 1 1 1 1 1 1 A/B/C/B/A 25/10/50/10 /25 LO CD CD oi τ-Η o wear 03 I ik 4-mercapto-p-pentene copolymer ◦ (bl)-a/(b2-l)/(b2-2) 0.06 35/15/50 ( Cl)-a/(c2)-a OO 〇· 30/70 1 1 1 1 1 1 A/B/C/B/A 25/10/50/10/25 inch LO CD oi οα os Example 1 4 - mercapto-1-pentaylene copolymer gi 1 cja g Λ ϊ 1 isigc=&gt; 35/15/50 (cl)-a/(c2)-a tH 20/80 1 1 1 1 1 1 A/ B/C/B/A 25/10/50/10/25 OO inch · οα CD S 〇IBp 1 1 ψ ◦ mass% 1 1 φ\ &lt;=) face c 1 1 Φ\ tea ο 1 1 φ\ 茶ο white 1 N/15mm 1 N/15mm painting ε resin type Ϊ 1 composition 1 I composition 1 ratio 1 resin species 1 δ3 layer thickness of each layer thickness heating and pressure treatment before the subsequent strength heating and addition Subsequent strength after pressure treatment exceeds φ4 Surface layer (A) Next layer (B) Buffer layer (c) Layer (D) s^s^s - X3 9 $SBS4 is f§s?l-iocdAp) (T§ Xs s^s^sss^i - xs 9^ifgft4: ◦1(0) ||^铋沭^墀装to·装 hl:Q—zq) inch S911s/60iA6/ffiii)_K?iiK distilling ^ΜΧίΝΐΓη 1294351 (2丨一&lt;) Example 10 4-mercapto-1-pentene-based copolymer g 1 i (bl)-a/(b2-l)/(b2-2) 0.06 35/15/50 (cl )-b/(c2)-a/(c2)-b CO cvi 20/60/20 (cl)-b CJi g A/B/C/D 25/10/50//25 τ—Η inch·CO (Ni &lt;NI ο another 03 I 4-mercapto-1-pentene-based copolymer g ι—Η cva 1 ( Λ i—4 i A cr&gt; 〇· 50/10/40 73 § Λ i—H oo ◦· 30/70 1 1 1 1 1 1 VB/C/B/A 25/10/50/10/25 CO LO 卜CNi rH ο in 〇〇¥ 4-mercapto-1-pentene-based copolymer gg A i H ! i &quot; H LO CN1 ◦· 20/30/50 (cl)-a/(c2)-a oo CD 30/70 1 1 1 1 1 1 A/B/C/B/A 25/ 10/50/10/25 inch (N 1 s CO Example 7 4-mercapto-1-1-pentene copolymer g τ—Η cji g r-jH έ Λ r^H g &lt;〇35/15/50 (cl)-a/(c2) -d LO rH 15/85 1 1 1 1 1 1 A/B/C/B/A 25/10/50/10/25 卜LO od (NI o CD I 4-mercapto-1-pentene Copolymers g ι—Η Cp H ^N r^H 0.06 35/15/50 (cl)-a/(c2)-c ΟΪ CO 30/70 1 1 1 1 1 1 A/B/C/B/A 25/10/50/10/25 OO ζό LO CO οα C3 gs olnp 1 1 ◦ ♦1 1 1 φ\ l CD s φ| ®DC 1 1 Marriage: o 1 1 ψ ◦ Mass % ε 3 -1 N/ 15mm N/15mm circumference B Resin type S Proportion composition I Jj % Proportion resin type I Thickness of each layer of the layered layer. Subsequent strength heating and pressure treatment before heating and pressure treatment: Substitute strength excess surface layer (A) Next layer (B) Buffer layer (c) Layer (9) ϋ 铋沭嚓 铋沭嚓 铋沭嚓 h h h h h h h h h h h h h h h h h h h h h h h h h h h h h h h h h h h h —§ q—(sf§ f(p)Ms (z丨§ (i) Ms inch eoo9 IIlr&gt;6/60^6/(t=3i)_s?ss fractionation/dx(NI ε 12943 t tender column 8 L/i 4-甲奸·系微8 r_— (bl)^/(b2-l)/(b2-2) ο Η 10/40/50 (cl)-a/(c2)-a 〇〇30 /70 WC7B/A 25/1 0/50/10/25 LO ◦· οα ◦· 寸g oo (column 7 4-Ape-contact system 8 1 (cl)-a/(c2)-a/(c2H LO 30/50/20 M7A 25 /70/25 1 1 1 1 CO CZ) LO (NI Bu_column 6 4-A-1) Copolymer g 1_ (cl)-^/(c2)-a 〇〇CD 30/70 A/C7A 25/ 70/25 1 1 1 1 but g delete 5 4-methyl·1_· copolymer gg Q (Ni g (c2)-a CM τ·-Η gii A/M7B/A 25/10/50/10/ 25 LO ◦· Τ-Η C5 CD § 匕_column 4 4-A H-liner copolymerization S rH s Λ 1 5 s ◦· 35/15/50 (c2)-a (N1 r-H s T-^ k/WUWK 25/10/50/10/25 m inch · C3 oi CO s oo thlii column 3 4-A trait scale copolymer g 9 &gt;si &gt; 0.06 35/15/50 (cl)-a/( C2)-a CD rH s A/M7B/A 25/10/50/10/25 oo inch · 1 &lt; oi CO C5 S butterfly 2 4-mercapto 4-contact copolymer g 1 έ &gt; /^N s 0.06 35/15/50 (cl)-a/(c2)-a &lt;=&gt; 60/40 WC7B/A 25/10/50/10/25 οα 00 τ—Η LO CO r—H t— H st tender column 1 4-A H-Jewish copolymerization ί Total s 1 έ &gt; /^NS 0.06 35/15/50 (cl)-a/(c2)-at-H o ◦' 70/30 A/ B/C/B/A 25/10/50/10/25 22.3 Bub·rH s & ί S Green! 1 1 ί AH &lt;=&gt; m〇t N/15mm N/15mm 1 ϊ 醤1 s ΟΛ 1 1 ί Lin Huan green thickness 53 Ϊ t ^ 2 3 excess &quot;mm*&quot;&quot;&quot;&quot;&quot; Table &f(A) Next layer (8) mmco 锲命铋爱ν-ιΫ5Η丨 inch 1) (i cd丨(lq) Διο 0丨§MsMs 17es9I^6/6s6/ff}«)_s^K^#/dx(NIcn 1294351 (73⁄4 t tender 歹丨 J15 4-甲壮麟 共聚 S r r bl (b)-a/(b2-l)/(b2-2) sc=&gt; 35/15/50 ! 30/70 ymm 25/10/50/10/25 LO 〇 J 1 LO § t tender column 14 4-mercaptopurine-liner copolymerization edge S 9 苕ss ◦· 35/15/50 (cl)-a/(c2)-f CO ◦· 30/70 A/M7B/ A 25/10/50/10/25 〇j Cvl CN1 § Canned J13 4-Azolla cymbal copolymer SC£5 &lt;=5 35/15/50 (cl)-a/(c2)-a Oo ◦· 30/70 mimik 25/10/50/10/25 LO CO (Νί oo § 列列 12 4-methyl 4-lane copolymerization S rH (bl&gt;a/(b2-l)/(b ^) ◦· 25/5/70 (cl)-a/(c2)-a oo 〇· 30/70 mimik 25/10/50/10/25 CNI C&lt;i CD CO § t-face 11 4-A &; 4-麟系徽徽s s (bl)-a/(b2-l)/(b2-2) |t-H c=&gt; 60/5/35 (cl)-a/(c2&gt;a oo C =) 30/70 rnmik 25/10/50/10/25 LO oi CO CO § 列列 10 4-曱H-麟系聚绿s s 9 1 SQ· 40/35/ 25 (cl)-a/(c2)-a OO 30/70 25/10/50/10/25 CO § Lai Lie 9 4-A Zhuanglin Copolymer miscellaneous sl-i 1 1 CO &lt;=&gt;* 20/50/30 (cl)-a/(c2)-a oo ◦· 30/70 mimik 25/10/50/10/25 05 inch! % % ! 1 1 ! 1 1 imc t Wldm N/15im t Ϊ 1 1 ΛΧ Ϊ 1 5 1 1 1 输 4 4 total level force tends ΜάΛ Table®^(A) mm) IIC〇二/^,,-Ν II τ—I &lt;ΝΙ /^Ν Ζ^Ν II τ—Η τ—· 〇νί CO JD JD Χ5 VS_^ · β—^ 丨 s svs^s—3^—^ S^S0^ ssfs s^sw^s4^n^^viii^&- ^

τ-Η (Nl &lt;NI (NI ο ο ο ο Sw/ 寸 2911 s/60tA6/ff&gt;紫)_ 恶縮s餾餾/dxCNIcn 1294351 (產業上之可利用性) 本發明之積層體,係耐熱性、離型性及緩衝性優良,同 時在FPC製造中加熱及加壓時,緩衝層之超出極少,可特 ^ 別適合使用作為FPC製造用之離型膜。 I 再者,以T-模具裝置進行之擠出成形,將可輕易製造 表面粗度與厚薄精度良好,且寬廣之膜,而具有極高之工 業性價值。τ-Η (Nl &lt;NI (NI ο ο ο ο Sw / inch 2911 s/60tA6/ff; purple) _ shrinking s distillation / dxCNIcn 1294351 (industrial availability) The layered body of the present invention It is excellent in heat resistance, release property and cushioning property, and when the heating and pressurization in FPC production, the buffer layer is extremely small, and it is particularly suitable for use as a release film for FPC production. The extrusion molding of the mold device makes it easy to manufacture a film having a large surface roughness and thickness, and a wide film, and has an extremely high industrial value.

312XP/發發明說明書(補件)/95-09/95116834 59312XP/Inventive Manual (supplement)/95-09/95116834 59

Claims (1)

1294351 十、申請專利範圍: ⑻曰者,立:=表面層⑴與緩衝層(C)之間具有接著層 八寺支為,该表面層(A)含有80〜100質量%之4_ 甲基—1-戊烯系聚合體,且嗜缓徐 、 ^ , V、友衝層(C)含有熔點190°c以 2如H Ό及熔點17代以下之軟質樹脂⑽。 .D申呀專利範圍第丨項之積層體,其 (β)係含有20〜50質量%之4_ \上述接者層 50〜8Π所旦。/ 甲基+戊稀系聚合體(bl)及 且以r = 含有碳原子數2〜4之烯烴的聚合體⑽, 未滿分:一C所測定之炼_ ^緩衝層⑹係含有10,質量%之熔點190〜25吖的 耐…性樹脂(cl)、及50〜90質量7ί) 17 、 樹脂(⑵,且以矜會?他 點7(M7GC的軟質 ' J且以何重2.16kg、溫度230它所測定之熔融产 動速率(MFR1)為0. 4〜l〇g/i〇分鐘。 刀L 3如申請專利範圍第2項之積層體,其中,上述 (B)係含有20〜50質量%之4-甲美]屮p5 曰 1,質敝乙稀.丁 J二基趙=聚合體⑽、 之卜丁㈣则(2)細―1)及3 W 如申請專利範圍第2項之積層體,其卜上述 «的耐熱性樹脂⑻係選自&quot;基+戊婦系聚合心 ^醯胺樹脂之至少1種,軟f樹脂⑽係選自低密 312XP/發發明說明書(補件y95-09/95丨丨6834 埽、直鏈狀低密度聚乙婦、高密度聚乙稀、丙稀之均 體、乙烯·丙烯共聚合體、乙烯·丙稀·丁烯共聚合體: 1294351 丁烯之均聚合體、乙、膝 ^ 合體及其等之順 :烯共聚合體、丙烯·丁烯共聚 5.如申請專利改質聚合體之至少-種。 (A)係含有4_甲&amp;弟2項之積層體,其中,上述表面層 與4-甲基+戊tΓ之均聚合體、或4~甲基—卜戊稀 體。 卜之碳原子數㈣之烯烴的共聚合 項之積層體,其中,積層體之至 及表面層(A)的厚度為積層體整 6 ·如申5青專利範圍第2 少一最外層為表面層(A), 體厚度的5〜50%。 严:二申叫專利範圍第2項之積層體,其中’加熱及加壓 _為基準測定:=緩衝層(C)之間以JIS d疋所传的接者強度為1〜20N/15mm。 ,丨、一 ^申明專利範圍第2項之積層體,其中,積層體之至 ^ 一最外層為表面層(A),該表面層(A)的面粗度Ry為 〇.〇1 〜20//Π10 ^ 如申請專利範圍第2項之積層體,其中,上述之各層 係藉由共擠出法而成形。 I 〇· —種離型膜,係含有申請專利範圍第丨至9項中任 一項之積層體。 II · 一種可撓性印刷電路基板製造用離型膜,係含有申 請專利範圍第1至9項中任一項之積層體。 31ZXP/發發明說明書(補件)/95-09/95116834 611294351 X. Patent application scope: (8) The latter, the vertical: = the surface layer (1) and the buffer layer (C) have an adhesive layer between the eight layers, and the surface layer (A) contains 80 to 100% by mass of 4_methyl- A 1-pentene-based polymer, and a slow-acting, ^, V, and a layer (C) contains a soft resin (10) having a melting point of 190 ° C and a melting point of 2 or less and a melting point of 17 or less. The layered body of the 专利 申 专利 专利 专利 专利 专利 专利 专利 专利 专利 专利 专利 专利 专利 专利 专利 专利 。 。 。 。 。 。 。 。 。 。 。 。 。 。 。 。 。 。 。 / Methyl + pentane polymer (bl) and a polymer (10) containing r = 2 to 4 olefins, not determined: a C measured by the _ ^ buffer layer (6) contains 10, quality % melting point 190~25吖 resistance resin (cl), and 50~90 mass 7 ί) 17 , resin ((2), and 矜 will? He point 7 (M7GC soft 'J and what weight 2.16kg, The melt production rate (MFR1) measured by the temperature 230 is 0.4 to 1 〇 g / i 〇 minutes. The knife L 3 is the laminate of the second item of the patent application, wherein the above (B) contains 20~ 50% by mass of 4-甲美]屮p5 曰1, 敝乙乙稀.丁J二基赵=Polymer (10), 卜丁(四)(2)细―1) and 3 W as patent application scope 2 The layered body of the item, wherein the heat resistant resin (8) is selected from at least one of the group + base group, and the soft f resin (10) is selected from the group consisting of low density 312XP/inventive specification ( Replenishment y95-09/95丨丨6834 埽, linear low-density polyethylene, high-density polyethylene, propylene homogenate, ethylene·propylene copolymer, ethylene·propylene/butene copolymer: 1294351 Butene Polymer, B, Knee, and the like: olefin copolymer, propylene and butene copolymer 5. At least one species of the patented modified polymer. (A) contains 4_A & a laminate body, wherein the surface layer is a homopolymer of 4-methyl+pentafluorene or a 4-methyl-p-pentamate, a layer of a copolymer of olefins having a carbon number (d), wherein The thickness of the laminated body and the thickness of the surface layer (A) is the laminated body. 6 · For example, the second patent of the 5th patent is the outermost layer of the surface layer (A), and the thickness of the body is 5 to 50%. It is called the laminated body of the second item of the patent range, in which 'heating and pressurizing _ is the benchmark measurement: = the strength of the joint transmitted by the JIS d疋 between the buffer layers (C) is 1~20N/15mm. ^ The layered body of claim 2, wherein the outermost layer of the laminated body is the surface layer (A), and the surface roughness Ry of the surface layer (A) is 〇. 〇1 〜20//Π10 ^ The laminate according to the second aspect of the patent application, wherein each of the above layers is formed by a co-extrusion method. I 〇·- a release film containing the patent application range 丨9 to 9. A laminated body for manufacturing a flexible printed circuit board, which comprises the laminated body of any one of claims 1 to 9. 31ZXP/Inventive Manual (Repair) /95-09/95116834 61
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