TW201231609A - Adhesive and adhesive film - Google Patents

Adhesive and adhesive film Download PDF

Info

Publication number
TW201231609A
TW201231609A TW100143855A TW100143855A TW201231609A TW 201231609 A TW201231609 A TW 201231609A TW 100143855 A TW100143855 A TW 100143855A TW 100143855 A TW100143855 A TW 100143855A TW 201231609 A TW201231609 A TW 201231609A
Authority
TW
Taiwan
Prior art keywords
adhesive
layer
weight
film
resin
Prior art date
Application number
TW100143855A
Other languages
Chinese (zh)
Other versions
TWI443172B (en
Inventor
Shigetomo Yamamoto
Atsushi Taga
Hirokazu Oki
Original Assignee
Toyo Boseki
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Toyo Boseki filed Critical Toyo Boseki
Publication of TW201231609A publication Critical patent/TW201231609A/en
Application granted granted Critical
Publication of TWI443172B publication Critical patent/TWI443172B/en

Links

Classifications

    • 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
    • C09J153/00Adhesives based on block copolymers containing at least one sequence of a polymer obtained by reactions only involving carbon-to-carbon unsaturated bonds; Adhesives based on derivatives of such polymers
    • C09J153/005Modified block copolymers
    • 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
    • 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
    • C09J11/00Features of adhesives not provided for in group C09J9/00, e.g. additives
    • C09J11/08Macromolecular additives
    • 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
    • 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
    • C09J153/00Adhesives based on block copolymers containing at least one sequence of a polymer obtained by reactions only involving carbon-to-carbon unsaturated bonds; Adhesives based on derivatives of such polymers
    • 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
    • C09J7/00Adhesives in the form of films or foils
    • C09J7/20Adhesives in the form of films or foils characterised by their carriers
    • C09J7/22Plastics; Metallised plastics
    • 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
    • C09J7/00Adhesives in the form of films or foils
    • C09J7/20Adhesives in the form of films or foils characterised by their carriers
    • C09J7/22Plastics; Metallised plastics
    • C09J7/24Plastics; Metallised plastics based on macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
    • C09J7/241Polyolefin, e.g.rubber
    • 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
    • C09J7/00Adhesives in the form of films or foils
    • C09J7/30Adhesives in the form of films or foils characterised by the adhesive composition
    • 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
    • C09J7/00Adhesives in the form of films or foils
    • C09J7/30Adhesives in the form of films or foils characterised by the adhesive composition
    • C09J7/35Heat-activated
    • 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
    • C09J7/00Adhesives in the form of films or foils
    • C09J7/30Adhesives in the form of films or foils characterised by the adhesive composition
    • C09J7/38Pressure-sensitive adhesives [PSA]
    • 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
    • C09J2203/00Applications of adhesives in processes or use of adhesives in the form of films or foils
    • C09J2203/318Applications of adhesives in processes or use of adhesives in the form of films or foils for the production of liquid crystal displays
    • 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
    • C09J2301/00Additional features of adhesives in the form of films or foils
    • C09J2301/10Additional features of adhesives in the form of films or foils characterized by the structural features of the adhesive tape or sheet
    • C09J2301/12Additional features of adhesives in the form of films or foils characterized by the structural features of the adhesive tape or sheet by the arrangement of layers
    • C09J2301/122Additional features of adhesives in the form of films or foils characterized by the structural features of the adhesive tape or sheet by the arrangement of layers the adhesive layer being present only on one side of the carrier, e.g. single-sided adhesive tape
    • 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
    • C09J2301/00Additional features of adhesives in the form of films or foils
    • C09J2301/30Additional features of adhesives in the form of films or foils characterized by the chemical, physicochemical or physical properties of the adhesive or the carrier
    • C09J2301/312Additional features of adhesives in the form of films or foils characterized by the chemical, physicochemical or physical properties of the adhesive or the carrier parameters being the characterizing feature
    • 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
    • C09J2423/00Presence of polyolefin
    • 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
    • C09J2423/00Presence of polyolefin
    • C09J2423/006Presence of polyolefin in the substrate
    • 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
    • C09J2423/00Presence of polyolefin
    • C09J2423/10Presence of homo or copolymers of propene
    • C09J2423/106Presence of homo or copolymers of propene in the substrate
    • 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
    • C09J2453/00Presence of block copolymer

Abstract

The present invention provides an adhesive and adhesive film which can be laminated without absence of lengthening of adhesive layer on substrate layer when coextruded by extruder and can be used in coating body of prism sheet etc. having small touch area with film when glued with protective film. The present invention provides an adhesion resin composition which is characterized by comprising resin composition containing adhesion granting resin not less than 2 parts in weight and less than 10 parts in weight and resin of polyolefin series not less than 2 parts in weight and less than 10 parts in weight relative to 100 parts in weight elastomer of styrene series having 5-15 wt% styrene component. The elastomer of styrene series takes block copolymer of styrene series copolymer blocks and olefin series copolymer blocks, block copolymer of styrene series copolymer blocks and random copolymer blocks of styrene and olefin, and/or these hydrogenated substances as main component.

Description

.201231609 六、發明說明: 【發明所屬之技術領域】 本發明係有關於一種黏著劑及黏著薄膜。本發明的 黏著劑係能夠適合使用於特収用以保護在光學用途所 使用之稜鏡片的棱型透鏡部的外表面之黏著薄膜。 又在用以保濩合成樹脂板(例如建築材料用)、不 鏽鋼板(例如建築材料用)、銘板、裝飾合板、鋼板、玻 璃板、家電製品、精密機械及製造時之汽車車體的表面 ,’用以在堆積、保存、輸送及製造步驟搬運時保護物品 避免,傷;以及在二次加工(例如彎曲加工和加壓加工) 時保護物品避免受傷之情況亦能夠冑合使用。 【先前技術】 以往’以保護被覆體的表面作為目的之黏著薄膜, 係被使用於建築材料、電氣、電子製品、汽車等的加工 :保存、輸送時,此種黏著薄膜係具有良好的黏著性, 同%在使用後,黏著劑必須 个霄1朵各表面而能夠輕易 剝下。 此種黏著薄膜係藉由在當作美姑沾昆l 士 而媒占n 一 在田作基材的層上積層黏著層 而構成。就黏者缚膜之塑沣士丄 __ 开胰您袈梃方法而言,例如可 合成樹脂等所構成之其好風 ^ . 、… 之基材層,塗布溶液狀的黏著劑之方 法,及將基材層、點著声尬遇把A秘 朽者層從钹數台擠出機熔融且 使用τ型模具等共擠出製膜 *衣胰之方法等。该等之中 、品質方面而言,以僅用Τ刑y目丄t 就成不 。 I杈八法之共擠出製膜為優越 用的樹 在進行共擠出製膜時,就使用於黏著層之有 1 201231609 ^ # D ’ ·5τ I ά熱m彈性體之一的苯乙烯系彈性體。 苯乙料彈性體係不僅是在製造薄料黏著層對包含聚 烯烴系樹脂之基材層的黏附力優良,而且具有藉由添加 黏著賦予劑而容易控制黏著力等之優點(專利文獻i)。 且說,近年來上述的被覆體由於多樣化,被覆面不 僅是平滑者’亦能夠看到許多具有表面凹凸者。就具有 表面凹凸之被覆體而言’例如可舉出使用於光學構件之 棱鏡片的棱型透鏡部#,對於如棱鏡片之具有表面凹凸 的被覆體,在使用上必須使充分的黏著力顯現。 因此,有以下的考量:以即便接觸面積較小亦能夠 得到黏著力的方式,接古& #„ ' 七:间黏者層的黏著力;或是藉由使 黏著層柔軟化]吏黏著層吃進被覆體的表面凹凸而增加 接觸面積來得到黏著力等。 為I謀求提升黏著層的自黏著性,係能夠藉由在適 口於黏著層之苯乙烯系彈性體添加黏著賦予樹脂(例如 參π專利文獻1等)。但是,由於在苯乙稀系彈性體添加 過剩的黏著賦予樹脂,將所構成的黏著層使用擠出機共 擠出而積層在基材層時’會產生黏著層的熔融黏度低落 且對於基材層難以延展而且費時之問題。X,使用供料 塊(feedblock)法積層8夺,在黏著層延展至基材層之後, 因為黏著層的炫融黏度係比基材層低,由於在薄膜寬度 方向:末端部黏著層會慢慢地產生裹包,致使末端部只 有黏著層@造成薄膜末端部黏著在製膜機等的問題。 又’藉由在苯乙稀系彈性體添加黏著賦予樹脂,能 夠使對於稜鏡片在使用上所必要的自身黏著力顯現(例 201231609 如參照專利文獻2) ’但是只有在苯乙稀系彈性體中添加 黏著賦予樹脂時’使薄膜成為捲筒狀態,在隨後將薄膜 捲出時,捲出性係未必良好。 [先前技術文獻] [專利文獻] [專利文獻1 ]曰本特開平1 〇 _ 1 5 1 6 5 6號公報 [專利文獻2]日本特開2007-3 323 29號公報 【發明内容】 [發明所欲解決之課題] 本發明所欲解決之課題係提供一種在製造黏著薄膜 時使用擠出機將黏著劑及基材層用樹脂進行共擠出之情 兄,能夠不產生延展不足而將黏著劑積層在基材層上, 而且在薄膜捲清狀下之黏結(b 1 〇 c k i n g)少,例如能夠適合 使用於與黏著薄膜的接觸面積小的稜鏡片等的被黏物之 點著劑及黏著薄膜。 [解決課題之手段] 本發明者等專心研討的結果,發現藉由使構成黏著 劑之樹脂組成在預定範圍,能夠解決上述的課題,而完 成了本發明》 亦即’本發明係一種黏著性樹脂組成物,其特徵在 於:包含相對於1 00重量份之苯乙烯系彈性體,含有2重 量份以上且小於1 0重量份的黏著賦予樹脂、2重量份以上 且小於1 0重量份的聚烯烴系樹脂之樹脂組成物;該苯乙 %系彈性體係苯乙稀成分為5〜15重量%,並且將苯乙稀 系聚合物嵌段與烯烴系聚合物嵌段的嵌段共聚物、笨乙.201231609 VI. Description of the Invention: [Technical Field of the Invention] The present invention relates to an adhesive and an adhesive film. The adhesive of the present invention can be suitably used for an adhesive film for protecting the outer surface of the prismatic lens portion of the cymbal used for optical applications. In addition, it is used to protect the surface of automobile bodies such as synthetic resin sheets (for building materials), stainless steel sheets (for building materials), name plates, decorative plywood, steel sheets, glass sheets, home appliances, precision machinery, and manufacturing. 'Used to protect articles from damage during the handling of stacking, storage, transport and manufacturing steps; and to protect articles from injury during secondary processing (such as bending and pressurization). [Prior Art] In the past, the adhesive film for the purpose of protecting the surface of the covering is used for processing of building materials, electrical and electronic products, automobiles, etc.: when the film is stored or transported, the adhesive film has good adhesion. , the same % after use, the adhesive must be smashed on each surface and can be easily peeled off. Such an adhesive film is formed by laminating an adhesive layer on a layer of a substrate as a substrate. The plastic film of the adhesive film is a method of applying a solution-like adhesive, such as a base material layer which is composed of a synthetic resin or the like, and a solution-like adhesive. And a method of co-extruding a film, a pancreas, and the like by melting a substrate layer and a sounding layer, and melting the A secret layer from a plurality of extruders. In terms of quality and quality, it is not possible to use only the gauntlet. The co-extrusion film of I 杈 eight method is a superior tree. When co-extrusion film is formed, it is used in the adhesive layer of styrene which has one of 201231609 ^ # D ' · 5τ I ά hot m elastomer Elastomers. The styrene-butadiene elastic system is excellent in adhesion to a base material layer containing a polyolefin resin in the production of a thin material adhesive layer, and has an advantage of easily controlling the adhesion by adding an adhesion-imparting agent (Patent Document i). In addition, in recent years, since the above-mentioned covering body is diversified, the covering surface is not only smooth, but also many surface irregularities can be seen. For the covering body having the surface unevenness, for example, the prismatic lens portion # used for the prism sheet of the optical member is used, and for the covering body having the surface unevenness as the prism sheet, it is necessary to exhibit sufficient adhesive force in use. . Therefore, there are the following considerations: the way to obtain adhesion even if the contact area is small, and the adhesion of the adhesive layer; or by softening the adhesive layer] The layer is eaten into the surface unevenness of the covering body to increase the contact area to obtain adhesion, etc. In order to improve the self-adhesiveness of the adhesive layer, it is possible to add an adhesive-imparting resin by adding a styrene-based elastomer to the adhesive layer (for example, π Patent Document 1, etc.) However, since an excessive adhesion-imparting resin is added to the styrene-based elastomer, the adhesive layer formed is coextruded by an extruder and laminated on the substrate layer to form an adhesive layer. The melt viscosity is low and it is difficult to extend and time-consuming for the substrate layer. X, using a feedblock method to build a layer, after the adhesive layer is extended to the substrate layer, because the adhesion layer is viscous viscosity The material layer is low, because in the width direction of the film: the adhesive layer at the end portion will slowly wrap, resulting in only the adhesive layer at the end portion, causing problems at the end of the film sticking to the film forming machine, etc. The addition of the adhesion-imparting resin to the ethylene-based elastomer allows the self-adhesive force necessary for the use of the enamel sheet to be exhibited (for example, 201231609, see Patent Document 2), but only when the adhesion-imparting resin is added to the styrene-based elastomer. 'The film is in a roll state, and when the film is subsequently taken up, the unwinding property is not necessarily good. [Prior Art Document] [Patent Document] [Patent Document 1] 曰本特开平1 〇 _ 1 5 1 6 5 6 [Patent Document 2] JP-A-2007-3 323 29 SUMMARY OF INVENTION [Problem to be Solved by the Invention] The problem to be solved by the present invention is to provide an adhesive to be used in the production of an adhesive film. When the agent and the substrate layer are coextruded with a resin, the adhesive can be laminated on the base material layer without causing insufficient expansion, and the bonding (b 1 〇cking) in the film winding state can be small, for example, It is suitable for the adhesive agent and the adhesive film which are used for the adherends, such as a smear which has a small contact area with the adhesive film. [Means for Solving the Problem] The inventors of the present invention have found that the composition is adhered by adhesion. The resin composition of the agent is in a predetermined range, and the above-mentioned problems can be solved, and the present invention is completed, that is, the present invention is an adhesive resin composition characterized by comprising a styrene-based elastomer in an amount of 100 parts by weight. a resin composition containing 2 parts by weight or more and less than 10 parts by weight of the adhesion-imparting resin, 2 parts by weight or more and less than 10 parts by weight of the polyolefin-based resin; the styrene-based elastomeric system styrene component is 5 ~15% by weight, and a block copolymer of a styrene-based polymer block and an olefin-based polymer block, stupid B

S 烯煙的無規共聚物嵌段之嵌 物作為主成分;該黏著性樹 _烴系樹脂的含量。 著薄膜時,即便是使用擠出 進行共擠出之情況’亦能夠 著劑積層在基材層上而成之 膜’其特徵在於:在將聚丙 層的一面積層上述黏著性樹 為保護薄膜,例如即便貼合 被覆體,亦具有實用上具有 薄膜之間重疊,黏著薄膜之 樹脂作為主成分之基材層, 物之黏著層相反的面,與脫 樹脂作為主成分之基材層、 著層、脫模層係以藉由共擠 笨乙烯系彈性體在230。〇、 flow rate ; MFR)係以 的聚丙稀系樹脂在2 3 〇 °c、 Μ 1 _0〜1 5g/10分鐘為佳。 201231609 稀系聚合物欲段及苯乙稀與 段共聚物、及/或該等的氫化 脂組成物之特徵係特別是聚 依照本發明,在製造黏 機將黏著劑及基材層用樹脂 付到不產生延展不足而將·袭占 黏著薄膜。 而且,本發明之點著薄 烯系樹脂作為主成分之基材 脂組成物而成。 本發明之黏著薄膜係作 在棱鏡片等具有表面凹凸之 充分的黏著力且即便將黏著 間的黏結亦少之優點。 又,在前述將聚丙烯系 以在與包含黏著性樹脂組成 模層積層而成為佳。 而且,前述將聚丙稀系 包含黏著性樹脂組成物之黏 出積層而成為佳。 而且,前述黏著層中的 2_16kgf之熔融流速(melt 0.5~10g/10分鐘為佳。The inclusion of the random copolymer block of S-ene smoke as a main component; the content of the adhesive tree-hydrocarbon resin. In the case of a film, even if it is coextruded by extrusion, it can be formed by laminating a film formed on a substrate layer. The adhesive layer of the one layer of the polyacryl layer is a protective film. For example, even if the coated body is bonded, there is a substrate layer which is practically composed of a film which is superposed between the films, and a resin which adheres the film as a main component, and a surface opposite to the adhesive layer of the object, and a base layer and a layer which are degreased as a main component. The release layer is at 230 by coextruding a stupid vinyl elastomer.聚, flow rate; MFR) is preferably a polypropylene resin of 2 3 〇 ° C, Μ 1 _0 to 1 5 g/10 minutes. 201231609 The rare polymer segment and the styrene and segment copolymer, and/or the hydrogenated fat composition are characterized, in particular, according to the invention, in the manufacture of the binder, the adhesive and the substrate layer are supplied with resin. It does not cause insufficient expansion and will occupy the adhesive film. Further, in the present invention, a thin epoxy resin is used as a base resin composition of a main component. The adhesive film of the present invention is advantageous in that it has sufficient adhesion to the surface unevenness such as a prism sheet, and the adhesion between the adhesives is small. Further, it is preferred that the polypropylene is laminated on the mold layer containing the adhesive resin. Further, it is preferable that the polypropylene contains an adhesive layer of an adhesive resin composition. Further, the melt flow rate of 2 to 16 kgf in the above-mentioned adhesive layer (melt 0.5 to 10 g/10 min is preferable).

而且,前述基材層中ί 2.1 6kgf之熔融流速(MFR)係J 201231609 而且,前述黏著薄膜係以稜鏡片被覆用為佳。 而且,前述黏著薄膜係以自身黏著性為佳。 [發明之效果] & 本發明之黏著層係在使用擠出機進行共擠出之 下,不產生延展不足而能夠將黏著劑積層在基 而且具有即便將黏著薄膜之間重疊,黏著薄 結亦少之優點。 本發明的黏著薄膜係例如在黏貼於稜鏡片等鱼 的接觸面積小之被黏物上作為保護薄膜時,具有充 黏著力,乃是有用的。 【實施方式】 [用以實施發明之形態] 以下,說明本發明的黏著劑及黏著薄膜之實施 。又’在本發明’稱為「作為主成分」時,係意味 成分為佔有90質量%以上。 (黏著性樹脂組成物) 就構成本發明的黏著劑之樹脂組成物而言,係 乙烯系彈性體、黏著賦予樹脂、聚烯烴系樹脂以預 率混合而成者,就在藉由共擠出而積層於將聚丙烯 脂作為主成分的基材層上時之延展性良好,而且在 供料塊(feed —k)法積㈣,在黏著層不容易在薄 寬度方向的末端部產生裹包且所得到的黏著薄膜係 對被覆體之自身黏著力方面,乃是較佳。 (苯乙烯系彈性體) 笨乙烯系彈性體係可舉出笨乙烯-丁二烯-笨乙 情況 上, 的黏 薄膜 分的 形態 著其 將苯 定比 系樹 使用 膜的 顯現 稀、 201231609 本乙沐··異戊二烯-苯乙稀、苯乙稀_乙烯/ 丁烯共聚物-苯 乙烯、笨乙烯-乙烯/丙烯共聚物-笨乙烯等的A_B_A型的 嵌段聚合物、苯乙烯.丁二烯、苯乙烯_異戊二烯、苯乙 烯-乙烯/丁烯共聚物、苯乙烯-乙烯/丙烯共聚物等的a_b 型嵌段共聚物、#乙烯-丁二烯橡膠等的#乙稀系無規共 1物及该等的氫化物。 在本發明所使用之苯乙烯系彈性體的氫化物,係意 謂源自上述苯乙烯系彈性體的共軛二烯之雙鍵係藉由^ 化而部分或完全飽和者。就飽和度而言,係以80mol%上. 為佳,以9〇m〇l%以上為更佳,以95〜1〇〇m〇1%為特佳。上 述飽和度小於80mol%時,會有黏著劑層的耐候性和耐熱 性不充分之情形。 苯乙烯系彈性體中的苯乙烯成分係以5重量%以上 15重量%以下為佳。小於5重量%時,製造樹脂時之造粒 係變為困難,大於丨5重量%時,黏著力低落且難以得到 必須的黏著力。又,黏著力係能夠藉由增加黏著賦予樹 脂的添加量而提升,但是隨著其添加量增加,共擠出時 黏著層的延展性變差^使用供料塊法積層時,黏著層容 易在薄膜的寬度方向的末端部產生裹包。為了顯現必須 的黏著力且使共擠出時黏著層的延展性良好,而且黏著 層不容易在薄膜的寬度方向的末端部產生裹包,苯乙烯 系彈性體中的苯乙烯成分係以丨0重量%以上丨3重量%以 下為佳。 所使用的苯乙烯系彈性體在230°C、2.1 6kgf之炼融流 速(MFR)係以〇 5〜1〇g/1〇分鐘的範圍為佳,就製膜性而言 201231609 ,係以2·〇〜8 〇g/I〇分鐘的範圍為更佳。 (黏著賦予樹脂) ::著賦予樹脂係例如可舉出脂肪族煙樹脂、芳香族 :tS烯樹脂、香豆酮·節樹脂、苯乙烯系樹脂、松 杳扣ί月曰專。 在樹脂组成物中之黏著賦予樹脂的含量,係相對於 100重量份之笨乙烯成分為5重量%以上15重量%以下的 苯土烯系彈性體,以2重量份以上且小於10重量份為佳。 黏:賦予樹脂的含量為小於2重量份時,係無法預期提升 黏著力。將黏著賦予樹脂過度地增加至10重量%以上時 ,在進行熔融擠出時’熔融黏度會顯著地低落。 將在230°c、2.16kgf之熔融流速(MFR)為小於i5(g/i〇 分鐘)之聚丙烯系樹脂系樹脂作為基材層並藉由共擠出 積層熔融黏度低的黏著層時,由於基材層與黏著層之間 的熔融黏度差異,會產生黏著層對於基材層難以^展且 費時之問題。又,使用供料塊法積層時,在黏著層延展 至基材層之後,因為黏著層的熔融黏度係比基材層低, 由於在薄膜見度方向的末部黏著層會慢慢地產生裹勺 ,致使末端部只有黏著層而造成薄膜末端部黏著在製膜 機等的問題。而且,將黏著薄膜捲取成為捲筒狀之後,' 再次捲出時亦有容易產生黏結之問題。又,因為亦有·亏 染被覆體之可能性。黏著賦予樹脂的含量係以4重量%以 上9重量%以下為佳。 (聚烯烴系樹脂) 聚烯烴系樹脂係沒有特別限定,可舉出結晶性聚丙 -10- 201231609 烯、丙烯與少量的α-烯烴之共聚物、低密度聚乙烯、高 密度聚乙烯、乙烯與少量的α·烯烴之共聚物、乙烯與乙 酸乙烯酯之共聚物等。其中’因為基材層係由聚丙烯系 樹脂所構成,故就熔融黏度等的關係而言,聚丙烯系樹 脂係能夠適合使用° 所使用之聚稀經系樹脂在23〇C、2.16kgf之炼融流速 (MFR),係以在0.5〜1 〇g/l 0分鐘的範圍為佳,基於製膜性 之點,以2.0〜8.0g/10分鐘的範圍為更佳。 在樹脂組成物中之聚烯烴系樹脂的含量,係相對於 100重量份之苯乙烯成分為5重量%以上15重量%以下的 苯乙烯系彈性體,為2重量份以上且小於i 〇重量份的範圍 。大於10重量份時,黏著力低落而無法得到對具有表面 凹凸的被覆體之充分的黏著力,而且延展性亦差。小於2 重量份時,將薄膜以捲筒狀態保存,隨後將薄膜捲出時 ’亦有產生黏結且薄膜部分地伸長、或變形等的問題。 聚稀烴系樹脂的含量係以4重量%以上9重量%以下為佳。 :,在黏著劑所使用的點著賦予樹脂,係依照種類 :有時候會含有一部分粉體,且有時候會在擠出時污毕 ^ . ,, , b约猎由將黏著賦予樹脂與聚烯 進行母料化而使用來改善,所以較佳是“著 予树脂與聚職系樹脂進行母料化而使用。 在本發明所使用之黏著劑 的課題之範圍,亦可按照須 不阻礙達成本發明 ;is丨 M要而添加交聯劑、點菩Ψ* 予劑、無機或有機填料、軟化#丨乂 W黏者性賦 、偶合劑、消泡劑、抗靜電劑 Τ塑劑、界面活性劑 4、阻燃劑等各種添加劑之1 β -11- 201231609 種或2種以上,以選擇不會阻礙黏著劑層和所得到的 薄膜(表面保護薄膜)的透明性之添加劑而使用為佳 (黏著薄膜) 使用上述黏著劑作為黏著劑層且藉由共擠出而 聚丙烯系樹脂作為主成分的基材層上積層而成之黏 膜’其黏著劑層係能夠充分地在基材層上延展。而 對棱鏡片等被覆體係具有充分的黏著力,並且具有 黏著薄膜之間重疊,黏著薄膜之間的黏結亦少之優 本發明之黏著薄膜的黏著力係在23下,對於 片為3〜50cN/25Cm的範圍,基於稜鏡片的保護性能之 疋較佳。黏著力小於3(;]^/25£;111時,在保護稜鏡片時 生捲縮等,而無法擔負作為保護薄膜之功能。另一 ,黏著力大於5〇cN/25cm時,在將薄膜從稜鏡片剝辦 有無法順利地剝離之虞。黏著力係能夠藉由變更黏 的樹脂組成和厚度等而適當地設定。 在本發明的黏著薄膜的黏著面對脫模面之剝離 係在2 3 C以1 0 0 c N / 2 5 c m以下的範圍,基於使黏著薄 捲筒形態時之薄膜的捲出性,乃是較佳。剥離力 100cN/25cm時,在使黏著薄膜成為捲筒形態時之薄 捲出’會產生薄膜部分性地伸長、或變形等的問題 離力係能夠藉由在脫模層形成表面凹凸,來變更捲 為捲筒時之黏著面與脫模面的接觸面積而適當地設 又’藉由在脫模層中添加氟樹脂、聚矽氧系樹脂、 基-1-戊烯聚合物等具有降低表面自由能的效果之 ,亦能夠降低剝離力。 黏著 在將 著薄 且, 即便 點。 稜鏡 點乃 會產 方面 時, 著層 力, 膜為 大於 膜的 。剝 取成 定。 4-甲 樹脂 -12- 201231609 本發明的黏著薄膜係能夠按照須 知的添加劑。例如亦其 、含有眾所周 安定劑、抗氧化劑、抗靜電柷黏結劑、熱 等。 M、耐衝擊改良劑 但是,以使黏著層表面的低分 lmg/m2為伟。尤+ 卞里物質A,丨 巧佳在此,測定黏著層表買為小於 依照以下順序而實施。使用乙 “子量物質係 的樹脂之有機溶劑將黏著層表面洗淨之:蝕構成黏著層 等從其洗淨液除去有機溶劑等之後,蒸發器 求得之數值除以黏著声表 ,、殘渣而將所 I層表面的表面積來求得。 在此’殘渣係存在lmg/m2以上時,在黏著層表面與 被黏物表面之間係有異物存在,因為會減少接觸面積而 造成凡得瓦力低落’故黏著力低落,乃是不佳。添加添 力:劑時’係必須選擇高分子型等的添加劑、或檢討添加 量及添加方法等而使其不會移行、轉印至黏著層。 (基材層) 本發明的黏著薄膜’係需要以聚丙烯系樹脂作為主 成分的基材層。就在此所使用之聚丙烯系樹脂而言,可 舉出結aa性聚丙烤、丙烯與少量的α_稀烴之無規共聚物 、喪段共聚物等。而且,更詳細地就結晶性聚丙烯系樹 脂而言,可舉出在通常的擠出成形等所使用之正庚烷不 溶性的同排(isotactic)聚丙烯同元聚合物、或含有60重量 %以上的丙烯之聚丙烯與其他的α_烯烴之共聚物,且能夠 將該丙烯同元聚合物或是丙烯與其他的α_烯烴之共聚物 單獨或混合使用。 201231609 在此,所謂正庚烷不溶性,係作為聚丙烯的結晶性 之指標且同時顯示安全性者,纟本發明,係以使用適合 昭和57年(1982年)2月日本厚生省公告第2〇號之正庚烷 不溶性(25°C、60分鐘萃取時的溶出部分為i5〇ppm以下[ 使用溫度為大於1〇〇。〇者係30ppm以下])者為較佳態樣。 就丙烯與其他的α -烯烴之共聚物的^烯烴共聚合成 分而言,係碳數為2〜8的α·烯烴,例如以乙烯或卜丁烯、 卜戊烯、1-己烯、4_曱基]戊烯等以以上的〇_烯烴為佳 在此所謂共聚物,係以將丨種或2種以上之在上述所 例示的α -烯烴對丙烯進行聚合而得到之無規或嵌段共聚 物為佳。 基於上述的理由,所使用之聚丙烯系樹脂在23〇r、 g之熔融机速(mfr),係以丨0〜15g/1〇分鐘的範圍為 佳,以2.0〜i〇.0g/1〇分鐘的範圍為更佳。 又’亦能夠將丙烯與其他的α•烯烴之共聚物混合2種 以上而使用。 而且’亦能夠將本發明中所得到的薄膜進行製品加 工時所產生的廢薄膜,作為回收原料而再造粒且添加在 基材層。藉由使用时原料,能夠抑制生產成本。 /在本發明的黏著薄膜中之黏著層對基材層之延展性 係=9〇 ’°以上為佳。若黏著層的延展性低’在取代樹 脂時需要花費;全 賈F夕的時間且操作性變差。又,以數μηι等 級使黏著層積層時,古 — 、 有在溥膜的寬度方向容易產生厚度 不均之問題。黏著斧的证s a ^ 者潜的延展性係以9〇%以上為佳,以93〇/〇Further, in the above-mentioned base material layer, the melt flow rate (MFR) of ί 2.1 6 kgf is J 201231609. Further, the adhesive film is preferably coated with a crepe sheet. Further, the adhesive film is preferably self-adhesive. [Effects of the Invention] The adhesive layer of the present invention is capable of laminating an adhesive on a base without coextrusion by using an extruder, and having an adhesive layer even if the adhesive films are overlapped. There are also few advantages. The adhesive film of the present invention is useful, for example, when it is adhered to a adherend having a small contact area of fish such as a crepe sheet as a protective film. [Embodiment] [Mode for carrying out the invention] Hereinafter, the implementation of the adhesive and the adhesive film of the present invention will be described. When the present invention is referred to as "main component", it means that the component is 90% by mass or more. (Adhesive resin composition) The resin composition constituting the adhesive of the present invention is obtained by co-extrusion of a vinyl-based elastomer, an adhesion-imparting resin, and a polyolefin-based resin at a pre-rate. When the laminate is laminated on the base material layer containing the polypropylene resin as a main component, the ductility is good, and in the feed block (feed-k) method (4), the adhesive layer is not easily wrapped in the end portion in the thin width direction. Further, the obtained adhesive film is preferred for the adhesion of the covering itself. (Styrene-based elastomer) The stupid vinyl-based elastomer system is in the form of a stupid ethylene-butadiene-stupid B. The form of the adhesive film is thin, and the film of the benzene-based system is thin. 201231609 Mu · isoprene - styrene, styrene - ethylene / butene copolymer - styrene, stupid ethylene - ethylene / propylene copolymer - stupid ethylene, etc. A_B_A type block polymer, styrene. #a-type block copolymer such as butadiene, styrene-isoprene, styrene-ethylene/butene copolymer, styrene-ethylene/propylene copolymer, etc. #乙乙丁丁橡胶# Rarely random a total of 1 and such hydrides. The hydride of the styrene-based elastomer used in the present invention means that the double bond of the conjugated diene derived from the above styrene-based elastomer is partially or completely saturated by chemical conversion. In terms of saturation, it is preferably 80 mol% or more, more preferably 9 〇m 〇 l% or more, and particularly preferably 95 〜1 〇〇 m 〇 1%. When the above saturation is less than 80 mol%, the weather resistance and heat resistance of the adhesive layer may be insufficient. The styrene component in the styrene elastomer is preferably 5% by weight or more and 15% by weight or less. When the amount is less than 5% by weight, the granulation in the case of producing a resin becomes difficult, and when it is more than 5% by weight, the adhesion is lowered and it is difficult to obtain a necessary adhesive force. Further, the adhesion can be improved by increasing the amount of adhesion imparted to the resin, but as the amount of addition increases, the ductility of the adhesive layer deteriorates during coextrusion. When the laminate is laminated by using a feedblock method, the adhesive layer is easily The end portion of the film in the width direction is wrapped. In order to exhibit the necessary adhesive force and to make the adhesive layer have good ductility during coextrusion, and the adhesive layer is not easily wrapped in the end portion in the width direction of the film, the styrene component in the styrene elastomer is 丨0. It is preferably 3% by weight or more and 3% by weight or less. The styrene-based elastomer to be used has a smelting flow rate (MFR) of 2.16 kgf at 230 ° C and a range of 〇 5 to 1 〇 g / 1 〇 minutes, and in terms of film formability, 201231609, is 2 · 〇 ~ 8 〇 g / I 〇 minutes range is better. (Adhesive-imparting resin) The resin-based resin may, for example, be an aliphatic smoky resin, an aromatic: tS olefin resin, a coumarone-segment resin, a styrene resin, or a squid. The content of the adhesion-imparting resin in the resin composition is 5% by weight or more and 15% by weight or less based on 100 parts by weight of the stupid ethylene component, and is 2 parts by weight or more and less than 10 parts by weight. good. Viscosity: When the content of the resin is less than 2 parts by weight, the adhesion is not expected to be improved. When the adhesion-imparting resin is excessively increased to 10% by weight or more, the melt viscosity is remarkably lowered during melt extrusion. When a polypropylene resin-based resin having a melt flow rate (MFR) of 2.16 kgf at 230 ° C and a flow rate (MFR) of less than i5 (g/i 〇 minute) is used as a base material layer, and an adhesive layer having a low melt viscosity is deposited by co-extrusion, Due to the difference in melt viscosity between the substrate layer and the adhesive layer, there is a problem that the adhesive layer is difficult to perform and time consuming for the substrate layer. Moreover, when the adhesive layer is used to laminate, after the adhesive layer is extended to the base material layer, since the adhesive layer has a lower melt viscosity than the base material layer, the adhesive layer is slowly formed at the end in the film visibility direction. The spoon causes the end portion to have only an adhesive layer and causes the film end portion to adhere to the film forming machine or the like. Further, after the adhesive film is taken up into a roll shape, there is a problem that adhesion tends to occur when it is rolled out again. Also, because there is also the possibility of losing the coated body. The content of the adhesion-imparting resin is preferably 4% by weight or more and 9% by weight or less. (Polyolefin-based resin) The polyolefin-based resin is not particularly limited, and examples thereof include crystalline polypropylene-10-201231609, a copolymer of propylene and a small amount of α-olefin, low-density polyethylene, high-density polyethylene, and ethylene. A small amount of a copolymer of α-olefin, a copolymer of ethylene and vinyl acetate, and the like. In the case where the base material layer is made of a polypropylene resin, the relationship between the melt viscosity and the like, the polypropylene resin can be suitably used. The polysulfide resin used at ° is 23 〇 C, 2.16 kgf. The smelting flow rate (MFR) is preferably in the range of 0.5 to 1 〇g/l 0 minutes, and more preferably in the range of 2.0 to 8.0 g/10 minutes based on the film forming property. The content of the polyolefin-based resin in the resin composition is from 5% by weight to 15% by weight based on 100 parts by weight of the styrene component, and is 2 parts by weight or more and less than i 〇 by weight. The scope. When the amount is more than 10 parts by weight, the adhesive strength is low, and sufficient adhesion to the covering having surface unevenness is not obtained, and the ductility is also poor. When the amount is less than 2 parts by weight, the film is stored in a roll state, and then when the film is taken up, there is a problem that the film is partially bonded, or the film is partially elongated or deformed. The content of the polyolefin resin is preferably 4% by weight or more and 9% by weight or less. :, in the point of use of the adhesive, the resin is given according to the type: sometimes it will contain a part of the powder, and sometimes it will be stained when it is extruded. Since the olefin is used for the masterbatch and is used for improvement, it is preferably used for the masterbatch of the resin and the poly-resin resin. The range of the problem of the adhesive used in the present invention may be achieved without hindering the achievement. The invention relates to the addition of a crosslinking agent, a sputum, a pre-agent, an inorganic or organic filler, a softening agent, a deodorant, a defoaming agent, an antistatic agent, a plasticizer, and an interface. 1 β -11 - 201231609 or more of various additives such as the active agent 4 and the flame retardant, and it is preferable to use an additive which does not inhibit the transparency of the adhesive layer and the obtained film (surface protective film). (Adhesive film) The adhesive film formed by laminating a layer of a substrate on which a polypropylene resin is used as a main component by using the above-mentioned adhesive as an adhesive layer can be sufficiently adhered to the substrate layer. Extension, and the coating system such as the prism sheet Adhesive force, and adhesion between the adhesive films, the adhesion between the adhesive films is less. The adhesive force of the adhesive film of the present invention is 23, and the film is based on the range of 3 to 50 cN/25 cm. The protective performance is better. The adhesion is less than 3 (;] ^ / 25 £; 111, when the cymbal is protected, curling, etc., can not afford the function as a protective film. Another, the adhesion is greater than 5 〇 At cN/25 cm, the film may not be smoothly peeled off from the crepe sheet. The adhesive force can be appropriately set by changing the resin composition and thickness of the adhesive, etc. The adhesive film of the adhesive film of the present invention is faced. The peeling of the release surface is preferably in the range of 1 3 0 C N / 25 cm or less in the range of 2 3 C, and is preferably based on the roll-out property of the film when the thin roll is adhered. When the peeling force is 100 cN/25 cm When the adhesive film is in the form of a roll, it is thinned out, and the film may be partially elongated or deformed. The force can be changed by forming the surface unevenness in the release layer to change the roll into a roll. Appropriate contact area between the adhesive surface and the release surface It is also possible to reduce the peeling force by adding a fluororesin, a polyoxymethylene resin, a ketone-1-pentene polymer or the like to the release layer, thereby reducing the peeling force. The adhesion is thin and Even if it is a point, it is a production point, the layer is strong, and the film is larger than the film. The stripping is determined. 4-Methyl Resin-12- 201231609 The adhesive film of the present invention can be used according to the known additives. It contains a lot of tranquilizers, antioxidants, antistatic enamel binders, heat, etc. M. Impact modifiers, however, to make the low score of the surface of the adhesive layer lmg/m2 Wei. Here, the measurement of the adhesive layer is performed in less than the following order. The surface of the adhesive layer is washed by using an organic solvent of a resin of a sub-quantity substance: after the etching constitutes an adhesive layer or the like, the organic solvent is removed from the cleaning liquid, etc., the value obtained by the evaporator is divided by the adhesion sound table, and the residue The surface area of the surface of the layer I is obtained. When the residue is more than 1 mg/m2, foreign matter is present between the surface of the adhesive layer and the surface of the adherend, because the contact area is reduced and the van der Waals is caused. The force is low, so the adhesion is low, but it is not good. When adding the force: when the agent is selected, it is necessary to select an additive such as a polymer type, or to check the addition amount and the addition method so that it does not migrate and transfer to the adhesive layer. (Base material layer) The pressure-sensitive adhesive film of the present invention requires a base material layer containing a polypropylene resin as a main component. The polypropylene resin used herein may be a a-propylene polypropylene or a propylene resin. A random copolymer of a small amount of α-dilute hydrocarbon, a smothered copolymer, etc. Further, the crystalline polypropylene-based resin in more detail may be a n-heptane used in usual extrusion molding or the like. Insoluble in the same row (isotacti c) a polypropylene homopolymer, or a copolymer of polypropylene containing 60% by weight or more of propylene and other α-olefins, and capable of copolymerizing the propylene homopolymer or propylene with other α-olefins It is used alone or in combination. 201231609 Here, the n-heptane-insoluble property is an indicator of the crystallinity of polypropylene and shows safety at the same time. The present invention is suitable for use in Japan in February of the Showa 57 (1982). The n-heptane insoluble of the No. 2 nickname of the Ministry of Health and Welfare is the best in the case where the elution portion at 25 ° C and 60 minutes of extraction is i5 〇 ppm or less [the use temperature is greater than 1 〇〇. The 系 is 30 ppm or less] In the olefin copolymerization component of the copolymer of propylene and another α-olefin, an α-olefin having a carbon number of 2 to 8, for example, ethylene or butylene, pentene, 1-hexene, 4_mercapto] pentene or the like is preferably the above-mentioned oxime, and the copolymer is obtained by polymerizing propylene with two or more kinds of the above-exemplified α-olefins. Block copolymers are preferred. For the above reasons, the polypropylene used The melting speed (mfr) of the resin at 23 〇r, g is preferably in the range of 〜0 to 15 g/1 〇min, and more preferably in the range of 2.0 to 〇.0 g/1 〇 min. Two or more kinds of copolymers of propylene and another α-olefin can be used in combination. Moreover, the waste film produced when the film obtained in the present invention is processed can be regranulated and added as a raw material to be recovered. In the base material layer, the production cost can be suppressed by using the raw material. / The adhesive layer in the adhesive film of the present invention is preferably more than 9 〇'° or more to the base layer. If the adhesive layer is ductile The low 'requires cost when replacing the resin; the time is good and the operability is deteriorated. In addition, when the adhesive layer is laminated with a number of μηι, there is a problem that the thickness is uneven in the width direction of the ruthenium film. . The certificate of sticking axe is better than 9〇%, and 93〇/〇

S -14- 201231609 以上為更佳,以95%以上為特佳。 在本發明的黏著薄 、之黏者層對基材層之裹包率系 以3 %以下為佳,黏著層义 ’’ iS ^ ^ . 晨I率向時,薄膜末端部係只 有黏者層’會發生黏著在制 t膜機等的問題,致使操作性 變差。黏著層對基材房夕宠 耵丞柯層之裹包率係以2.5〇/〇以下為更佳。 在本發明的黏著薄膜之黏著層的厚度,係以1陣以 士、小於30,為佳。黏著薄膜的厚度小於⑽時,難以 藉由共擠出而安定地製膜 心奶表犋,30μιη以上時,則為在成本方 面不利的薄膜。此時,佶 吏點者力增大時,考慮其黏性以 增加厚度為佳。藉由增加黏著層的厚纟,與被黏物的接 觸面積係容易變大。點著層的厚度係以以上20_以 下為佳,以3μηι以上15μιη以下為更佳,以以上8_以 下為特佳。 在本發明的黏著薄膜之基材廣的厚度,係以5 μ m以上 於ΙΟΟμιη為佳,以15μιη以上且小於25μπι為更佳。黏 著薄膜的厚度小於5μ〇ι時強韌感變弱,貼在被覆體作為保 濩薄膜蚪,有容易產生皺紋且無法充分地得到黏著力之 問題1 以上時’則為在成本方面不利的薄膜。 (脫模層) ' 本發明的黏著薄膜,係以在與基材層的一面所積層 之黏著層相反的面形成脫模層為佳。藉由如此進行,能 夠進步抑制黏結。鑒於本發明的黏著層之樹脂組成, 以使脫模層表面的平均表面粗糙度SRa為〇 4〇μιη以上為 佳。以成為表面的平均表面粗糙度SRa為0 850μιη以下之 表面為佳,以〇.5〇〇μιη以上〇 7〇〇μιη以下為特佳。脫模層S -14- 201231609 The above is better, with 95% or more being the best. In the adhesive film of the present invention, the adhesion layer of the adhesive layer to the substrate layer is preferably 3% or less, and the adhesive layer is ''iS ^ ^.) When the morning I rate is normal, the film end portion is only the adhesive layer. 'There will be problems such as adhesion to the t-film machine, resulting in poor workability. Adhesive layer on the substrate room 夕 耵丞 耵丞 层 层 层 层 层 层 层 层 层 层 层 层 层 层 层 层 层 层 层 层The thickness of the adhesive layer of the adhesive film of the present invention is preferably one or less than 30. When the thickness of the adhesive film is less than (10), it is difficult to form a core milk gluten by coextrusion, and when it is 30 μm or more, it is a film which is disadvantageous in terms of cost. At this time, when the force of the 佶 吏 is increased, it is preferable to consider the viscosity to increase the thickness. By increasing the thickness of the adhesive layer, the contact area with the adherend tends to become large. The thickness of the spot layer is preferably 20 or less, more preferably 3 μηη or more and 15 μιη or less, and more preferably 8 or less. The thickness of the substrate of the adhesive film of the present invention is preferably 5 μm or more and more preferably 15 μm or more and less than 25 μm. When the thickness of the adhesive film is less than 5 μm, the toughness is weakened, and it is applied to the coated body as a protective film, and wrinkles are likely to occur and the adhesive force is not sufficiently obtained. When it is more than the above, it is a film which is disadvantageous in terms of cost. . (Release layer) The adhesive film of the present invention preferably has a release layer formed on a surface opposite to the adhesion layer formed on one surface of the base material layer. By doing so, it is possible to progress to suppress the adhesion. In view of the resin composition of the adhesive layer of the present invention, the average surface roughness SRa of the surface of the release layer is preferably 〇 4 〇 μηη or more. It is preferable that the surface having an average surface roughness SRa of 0 850 μm or less is preferably 〇.5 〇〇μηη or more 〇 7 〇〇 μηη or less. Release layer

S -15- 201231609 的厚度係以Ιμιη以上且小於3〇pm為佳,以3〜1〇μιη為特 佳。 為了形成如上述的表面凹凸,能夠藉由使用丙烯· 乙烯嵌段共聚物而形成粗糙無光澤狀且表面粗糙的層。 又,藉由在同元聚丙烯中混合聚乙烯系樹脂亦能夠期待 同樣的效果。並且藉由在丙烯-乙烯嵌段共聚物中混合聚 乙烯系樹脂亦能夠形成表面更粗糙的層。就適合於得到 粗糙無光澤狀的表面之樹脂而言,具體上,能夠例示曰 本POLYPRO(股)製的「BC4FC」等的丙烯_乙烯嵌段共聚 物。 在操作上,本發明的黏著薄膜係以捲筒的形態為適 合。薄膜捲筒的寬度及捲取長度的上限係沒有特別限制 ,基於操作的容易性,通常係寬度為1.5m以下,並且薄 膜厚度為30μιη時,捲取長度係以6〇〇〇111以下為佳。又, 通常能夠使用3英叶、6英时、8英忖等的崎芯和金 芯作為捲取芯。又’從加工的適合性而言,以使用長卢 以上、寬度45〇職以上的尺寸捲取而成之薄膜捲^ 為了要保護光學用途所使用之稜鏡片的稜 料表面,可特別適合運用使用本發明的黏著劑之黏^ 溥膜。又,為了要保護合成樹脂板(例如建築材料用 不鑛鋼板7如建築材料用)、純、裝飾合板、鋼板I 玻璃板、家電製品、精密機械及製造時之汽車車體 面’為了要在堆積、保存、輸送及製造步驟中搬運時伴 護物品避免受傷;以及在二次加工(例如彎曲加工=The thickness of S -15- 201231609 is preferably Ιμηη or more and less than 3 〇 pm, and is preferably 3 to 1 〇 μιη. In order to form the surface unevenness as described above, a layer having a rough matte appearance and a rough surface can be formed by using a propylene/ethylene block copolymer. Further, the same effect can be expected by mixing a polyethylene resin in the homopolypropylene. Further, a layer having a rougher surface can be formed by mixing a polyethylene-based resin in the propylene-ethylene block copolymer. Specifically, a propylene-ethylene block copolymer such as "BC4FC" manufactured by POLYPRO Co., Ltd. can be exemplified as the resin which is suitable for obtaining a surface having a rough matte shape. In operation, the adhesive film of the present invention is suitably in the form of a roll. The width of the film roll and the upper limit of the winding length are not particularly limited, and based on the ease of handling, the width is usually 1.5 m or less, and when the film thickness is 30 μm, the winding length is preferably 6 〇〇〇 111 or less. . Further, it is generally possible to use a core and a core of 3 inches, 6 inches, and 8 inches as a winding core. In addition, it is a film roll that is rolled up to a size of 45 or more in width and above, and is suitable for use in protecting the edge of the ruthenium used for optical applications. The adhesive film of the adhesive of the present invention is used. In order to protect the synthetic resin sheet (for example, non-mine steel plate 7 for building materials such as building materials), pure, decorative plywood, steel plate I glass plate, home appliances, precision machinery, and automobile body surface when manufacturing Contamination, storage, transportation, and manufacturing steps to avoid injury when handling; and in secondary processing (such as bending processing =

-16- S 201231609 加工)時保護物品避免受傷之情況亦能夠適合使用。 [實施例] 以下舉出實施例而進一步說明本發明。但是只要不 脫離其要旨,本發明不被下述的實施例限定。又,下述 的實施例、比較例之物性的評價方法係如以下。 (1) 黏著層對基材層之延展性的評價 在3層T型模具(供料塊型、模唇寬度85〇nim、模唇間 隙1mm)内,使用4〇mm φ單轴擠出機將黏著層樹脂以 15kg/小時的吐出量;使用9〇mm φ單軸擠出機將基材層 樹脂以15kg/小時的吐出量;及使用6〇mm φ單軸擠出機 將脫模層樹脂以5kg/小時的吐出量各自進行共擠出。藉 由將擠出的薄膜以20m/分鐘的速度牽引至溫度為3 〇〇c的 鑄造滾筒’而得到650mm寬度之未延伸薄膜。將黏著層 樹脂投入40mm φ單轴擠出機,測定從該樹脂開始取代經 過30分鐘後之黏著層對基材層的延展率。 延展率=黏著層的積層寬(mrn)/6 5 0(mm)x 1〇〇(%) (2) 黏著層對基材側之裹包性的評價 在3廣T型模具(供料塊型、模唇寬度85〇ιηιη、模唇間 隙lmm)内,使用40mm φ單轴擠出機將黏著層樹脂以 15kg/小時的吐出量;使用90mmφ單軸擠出機將基材層 樹脂以15kg/小時的吐出量;及使用65ιηιηφ單軸擠出^ 將脫模層樹脂以5kg/小時的吐出量各自進行共擠出。夢 由將擠出的薄膜以20m/分鐘的速度牵引至溫度為3〇(5c的 鑄造滾筒,而得到650mm寬度之未延伸薄膜。將黏著層 樹月曰投入40mm φ單軸擠出機’測定從該樹脂開始取代柄 201231609 過1 20分鐘後之黏著層對基材層之薄膜寬度方向的兩端 的裹包率。 裹包率=黏著層在薄膜寬度方向的兩端所裹包的寬度 (mm)/650(mm)xl00(%) (3)黏著性的評價 依據JIS-Z-023 7(200 0)黏著膠帶·黏著薄片試驗方法 且使用下述的方法測定。 準備壓克力板(Mitsubishi Rayon(股)製:Acrylight( 註冊商標)3mm厚)5〇mmx 1 50mm、不同表面處理狀態之2 種複鏡片(透鏡部係由三角柱所構成,三角柱的高度為 25μηι、二角柱的寬度為5〇μηι) 50mmxl50mm作為被黏物 ’切取沿在薄膜製造時的捲取方向1 5 〇 m m、沿與其正交 的方向25mm的試片作為試片,且使用質量為2000g的橡 膠輥(輥表面的彈簧硬度為80Hs、被厚度為6mm的橡膠層 被覆之寬度為45mm'直徑(包含橡膠層)為95niln者)以 5mm/秒的速度使其往返一次而將被黏物與試片壓黏。壓 •^占之後,將在溫度2 3 C、相對濕度為6 5 %的環境下經放置 3〇分鐘者’使用島津製作所(股)製「autograph(註冊 商標)」(AGS-J),以300mm/分鐘的速度18〇度剝離時之抵 抗值作為黏著力[cN/25cm]。所謂18〇度剝離,係意謂在 測定剝離時的抵抗值之際,使壓克力板與薄膜之剝離角 度保持在1 8〇度。 2備厚度為190μηι、尺寸為25mmXl7〇mm的聚酯片作 為測定時之測定試料的抓持部,在上述黏著薄膜與壓克 力板壓黏而成之測定試料的黏著薄膜末端部上,、使用黏-16- S 201231609 Processing) When the article is protected from injury, it can be used as appropriate. [Examples] Hereinafter, the present invention will be further described by way of examples. However, the present invention is not limited by the following examples without departing from the gist of the invention. Further, the evaluation methods of the physical properties of the following examples and comparative examples are as follows. (1) Evaluation of the ductility of the adhesive layer on the base layer In a 3-layer T-die (feed block type, lip width 85〇nim, lip gap 1 mm), a 4 mm mm φ single-axis extruder was used. The adhesive layer resin was discharged at a rate of 15 kg/hour; the substrate layer resin was discharged at a rate of 15 kg/hour using a 9 mmmm φ single-axis extruder; and the release layer was formed using a 6 mm mm φ single-axis extruder The resin was co-extruded at a discharge amount of 5 kg/hour. An unstretched film having a width of 650 mm was obtained by drawing the extruded film at a speed of 20 m/min to a casting drum of a temperature of 3 〇〇c. The adhesive layer resin was placed in a 40 mm φ single-axis extruder, and the elongation of the adhesive layer to the substrate layer after 30 minutes from the replacement of the resin was measured. Extensibility = stack width of the adhesive layer (mrn) / 6 5 0 (mm) x 1 〇〇 (%) (2) Evaluation of the wrapability of the adhesive layer on the substrate side in the 3 wide T-die (feed block) Type, lip width 85 〇ιηιη, lip gap lmm), using a 40mm φ single-axis extruder to discharge the adhesive layer resin at 15kg / hr; using a 90mm φ single-axis extruder to base material layer resin 15kg The amount of discharge per hour; and the uniaxial extrusion using 65 ηηιηφ ^ The release layer resin was co-extruded at a discharge amount of 5 kg / hour. The dream was to draw the extruded film at a speed of 20 m/min to a casting roll at a temperature of 3 〇 (5 c to obtain an unstretched film of 650 mm width. The adhesive layer was placed in a 40 mm φ single-axis extruder] The wrap ratio of the adhesive layer to the both ends of the substrate layer in the film width direction after the lapse of 20 minutes from the resin. The wrap ratio = the width of the adhesive layer wrapped at both ends in the film width direction (mm) / 650 (mm) xl00 (%) (3) Evaluation of adhesion According to JIS-Z-023 7 (200 0) Adhesive tape and adhesive sheet test method, and measured by the following method. Preparation of acrylic sheet (Mitsubishi) Rayon (stock): Acrylight (registered trademark) 3mm thick) 5〇mmx 1 50mm, two kinds of complex lenses in different surface treatment conditions (the lens part is composed of triangular prisms, the height of the triangular column is 25μηι, and the width of the prism column is 5 〇μηι) 50mmxl50mm as the adherend 'cut the test piece along the winding direction of the film at a winding direction of 15 mm, 25 mm in the direction orthogonal thereto as a test piece, and use a rubber roll having a mass of 2000 g (roller surface) The spring hardness is 80Hs and the thickness is 6mm. The rubber layer is covered with a width of 45 mm 'the diameter (including the rubber layer) is 95 niln), and the adhesive is pressed back to the test piece at a speed of 5 mm / sec. After pressing, the temperature is 2 3 C. The "autograph (registered trademark)" (AGS-J) manufactured by Shimadzu Corporation (shares) is used at a speed of 300 mm/min. The resistance value is used as the adhesive force [cN/25cm]. The so-called 18-degree peeling means that the peeling angle of the acrylic sheet and the film is maintained at 18 degrees in the measurement of the resistance value at the time of peeling. A polyester sheet having a size of 190 μm and a size of 25 mm×17 〇mm is used as a gripping portion for measuring a sample at the time of measurement, and a sticky film is used on the end portion of the adhesive film of the measurement sample obtained by adhering the adhesive film and the acrylic sheet.

-18- S 201231609 勝部為15mm寬度之Cellophane Tape(註冊商標)點貼而作 為測定時之抓持部。將測定試料的模式圖顯示在第丨圖。 測定係針對一個試樣實施3次而將其平妁信祚泛^ τ Θ值邗為該試料 的黏著力。 (4 )财黏結性的評價 如下述測定黏著薄膜的脫模層與黏著層之剥離力作 為耐黏結性的評價。 在壓克力板(Mitsubishi Ray on(股)製:Acry light 3mm 厚)5 Omm χ 15 0mm的全部面上黏貼雙面接著膠帶(日東電 工(股)製:No.535 A) ’且在雙面接著膠帶的另外—面上, 以試片靠過來的方式黏貼1 50mm(薄膜製造時的捲取方向 )x50mm(與薄膜製造時的捲取方向正交的方向)之試片。 切取沿在薄膜製造時的捲取方向1 5〇mm、沿與其正 父的方向25mm的試片作為新的試片,且將其黏著面與已 透過雙面接著膠帶貼在壓克力板上之試片的脫模面重疊 之後,使用質量為2000g的橡膠輥(輥表面的彈簧型硬度 為8 0Hs、被厚度為6 mm的橡膠層被覆之寬度為45111〇1、直 控(包含橡膠層)為95mm者)以5mm/秒的速度使其往返一 ••人而將脫模面與試片壓黏。壓黏之後,將在溫度2 3。匸、 相對濕度為65%的環境下經放置30分鐘者,使用島津製 作所(股)製「AUTOGRAPH(註冊商標)」(AGS_j),以 3 00mm/分鐘的速度180度剝離時之抵抗值作為剝離力 [cN/25mm]。 準備厚度為190μιη、尺寸為25mmxl70mm的聚酯片作 為測定時之測定試料的抓持部,在l5〇mmx25mm的試片 -19- ^ 201231609 之末端部,使用黏膠部為15111111寬度之Cellophane Tape( 註冊商標)黏貼而作為測定時之抓持部。測定係針對一個 试樣實施3次而將其平均值作為該試料的剝離力。 (5) 平均表面粗糙度之測定 使用小坂研究所(股)製之接觸式三維中心面表面粗 鏠度計(型式ET·30HK)’藉由觸針法且使用以下的條件測 定脫模層的表面之中心面平均粗糙度。條件係如下 述且以3次測定的平均值作為該值。 觸針前端半徑:〇.5μιη 觸針壓:20mg 截止值:80μπι 測定長度:ΙΟΟΟμιη 測定速度:ΙΟΟμιη/秒 測定間隔:2μηι (6) 操作性 使所得到的薄膜成為捲筒,將從捲筒把薄膜捲出時 之薄膜的抵抗較小者評價為〇,較大者為X。 [實施例1 ] (基材層的製造) 將聚丙烯系樹脂(住友化學製:FS201 1DG3、MFR : 2.5 g/10 mi η) 100 wt %使用90mm φ單軸擠出機熔融擠出而 成為基材層。 (黏著層的製造) 使用40mm φ單軸擠出機將相對於100重量份之苯乙 烯系彈性體(Asahi Kasei Chemicals製:TAFTEC(註冊商 s -20- 201231609 標)111221、苯乙烯共聚合比12”%、1^11:4.58/1〇11111〇 ’混合8 · 8重量份之聚丙烯系樹脂(住友化學製: FS201 1DG3、MFR : 2.5g/10min)及 8.8重量份之石油樹脂 (荒川化學工業製:Arkon(註冊商標)P125)而成者熔融擠 出而作為黏著層。 (脫模層的製造) 使用65mm φ單軸擠出機將100wt%之丙烯-乙烯嵌段 共聚物(Japan Polypropylene製:BC4FC)熔融擠出而作為 脫模層。 (薄膜的製造) 各自使用各擠出機將基材層、黏著層、脫模層直接 以熔融之狀態,在250°C的3層T型模具(供料塊型、模唇 寬度850mm、模唇間隙imm)内進行積層擠出。將擠出的 薄膜以20m/min速度牽引至溫度為3〇。〇之鑄造滾筒,冷卻 固化而得到基材層厚度為l8jim、黏著層厚度為6μιη、脫 模層厚度為6μηι之3種3層的未延伸薄膜。 [實施例2] 黏著層、脫模層係維持與實施例1相同,將基材層變 更為下述内容且使用與實施例1同樣的製法而得到3種3 層的未延伸薄膜。 (基材層的製造) 使用90mm φ單軸擠出機將i〇〇wt〇/〇之同元聚丙烯系 樹脂(住友化學製:FLX80E4(MFR : 7.5g/10min)熔融擠出 而成為基材層。 [實施例3]-18- S 201231609 The winner is a 15mm-width Cellophane Tape (registered trademark) and is used as a gripping unit for measurement. The pattern diagram of the measurement sample is shown in the figure. The measurement was carried out three times for one sample, and the value of the 妁 妁 ^ ^ τ was determined as the adhesion of the sample. (4) Evaluation of the adhesion property The peeling force of the release layer and the adhesive layer of the adhesive film was measured as the adhesion resistance. Apply double-sided adhesive tape (made by Nitto Denko Co., Ltd.: No. 535 A) on the entire surface of an acrylic plate (Mitsubishi Ray on: Acry light 3mm thick) 5 Omm χ 150 mm] On the other side of the tape, a test piece of 1 50 mm (winding direction at the time of film production) x 50 mm (direction orthogonal to the winding direction at the time of film production) was adhered to the test piece. A test piece taken along the winding direction of the film at a height of 15 mm and 25 mm in the direction of its parent is cut as a new test piece, and the adhesive face and the double-coated adhesive tape are attached to the acrylic plate. After the release faces of the test pieces were overlapped, a rubber roller having a mass of 2000 g was used (the spring type hardness of the roll surface was 80 hs, and the width of the rubber layer covered by the thickness of 6 mm was 45111 〇1, and the direct control (including the rubber layer) ) is 95mm). The mold release surface is pressed against the test piece at a speed of 5 mm/sec. After pressure bonding, it will be at a temperature of 2 3 . AU 匸 匸 AU AU AU AU AU AU AU AU AU AU AU AU AU AU AU AU AU AU AU AU AU AU AU AU AU AU AU AU AU AU AU AU AU AU AU AU AU AU AU AU AU AU AU AU AU AU AU AU AU AU AU AU AU AU AU AU AU AU AU Force [cN/25mm]. A polyester sheet having a thickness of 190 μm and a size of 25 mm×1 70 mm was prepared as a grip portion for the measurement sample at the time of measurement, and a Cellophane Tape having a width of 15111111 was used at the end portion of the test piece -19-^201231609 of 15 mm mm×25 mm. Registered trademark) is used as a gripping part for measurement. The measurement was carried out three times for one sample, and the average value thereof was taken as the peeling force of the sample. (5) Measurement of the average surface roughness The contact type three-dimensional center surface roughness meter (type ET·30HK) manufactured by Otaru Research Institute Co., Ltd. was used to measure the release layer by the stylus method and using the following conditions. The average roughness of the center of the surface. The conditions are as follows and the average value of the three measurements is taken as the value. Tip tip radius: 〇.5μιη Contact pin pressure: 20mg Cutoff value: 80μπι Determination length: ΙΟΟΟμιη Measurement speed: ΙΟΟμιη / sec Measurement interval: 2μηι (6) Operate the resulting film into a roll, which will be taken from the reel The film with less resistance when the film was rolled out was evaluated as 〇, and the larger one was X. [Example 1] (Production of base material layer) A polypropylene resin (manufactured by Sumitomo Chemical Co., Ltd.: FS201 1DG3, MFR: 2.5 g/10 mi η) 100 wt% was melt-extruded using a 90 mm φ uniaxial extruder. Substrate layer. (Manufacturing of Adhesive Layer) Using a 40 mm φ single-axis extruder, styrene copolymerization ratio with respect to 100 parts by weight of a styrene-based elastomer (manufactured by Asahi Kasei Chemicals: TAFTEC (registered company s-20-201231609) 111221, styrene copolymerization ratio 12"%, 1^11: 4.58/1〇11111〇' mixed 8 · 8 parts by weight of polypropylene resin (manufactured by Sumitomo Chemical Co., Ltd.: FS201 1DG3, MFR: 2.5g/10min) and 8.8 parts by weight of petroleum resin (Arakawa Chemical industry: Arkon (registered trademark) P125) The melt is extruded as an adhesive layer. (Manufacturing of release layer) 100 wt% of propylene-ethylene block copolymer (Japan) using a 65 mm φ single-axis extruder Polypropylene: BC4FC) melt-extruded to form a release layer. (Production of a film) The base layer, the adhesive layer, and the release layer were directly melted in each extruder using a three-layer T at 250 °C. The mold was extruded in a mold (feed block type, lip width 850 mm, lip gap imm). The extruded film was drawn at a speed of 20 m/min to a temperature of 3 Torr. The casting drum was cooled and solidified. The thickness of the substrate layer is l8jim, the thickness of the adhesive layer is 6μιη, and the release layer Three types of three-layer unstretched film of 6 μm is used. [Example 2] The adhesive layer and the release layer were maintained in the same manner as in Example 1, and the substrate layer was changed to the following and the same method as in Example 1 was used. Three kinds of three-layer unstretched films were obtained. (Manufacturing of a base material layer) A homopolymer polypropylene resin of i〇〇wt〇/〇 was produced using a 90 mm φ single-axis extruder (manufactured by Sumitomo Chemical Co., Ltd.: FLX80E4 (MFR: 7.5 g/10 min) melt-extruded to form a base material layer. [Example 3]

-21- S 201231609 基材層 '脫模層係維持與實施例1相同,將黏著層變 更為下述内容且使用與實施例1同樣的製法而得到3種3 層的未延伸薄膜。 (黏著層的製造) 使用40mm φ單軸擠出機將相對於1〇〇重量份之苯乙 烯系彈性體(Asahi Kasei Chemicals 製:TAFTEC H1221 、笨乙烯共聚合比12wt%、MFR : 4.5g/10min),混合3.2 重量份之石油樹脂(荒川化學工業製:Arkon P 1 25)及3.2 重量份之聚丙烯系樹脂(住友化學製:FS201 1DG3、MFR :2.5g/10min)而成者熔融擠出而作為黏著層。 [實施例4] 基材層、脫模層係維持與實施例1相同,將黏著層變 更為下述内容且使用與實施例1同樣的製法而得到3種3 層的未延伸薄膜。 (黏著層的製造) 使用40mm φ單軸擠出機將相對於10〇重量份之苯乙 烤系彈性體(Asahi Kasei Chemicals 製:TAFTEC H1221 、本乙稀共聚合比1 2 w t %、M FR · 4_5g/l〇min),混合8.8 重量份之石油樹脂(荒川化學工業製:Arkon P125)及8.8 重量份之聚丙烯系樹脂(住友化學製:WF83 6DG3、MFR :7.0g/10min)而成者炼融擠出而作為黏著層。 [實施例5 ] 脫模層係維持與實施例1相同,將基材層及黏著層變 更為下述内容且使用與實施例1同樣的製法而得到3種3 層的未延伸薄膜。-21-S 201231609 Base material layer The release layer was maintained in the same manner as in Example 1, and three kinds of three-layer unstretched films were obtained by the same method as in Example 1 except that the adhesive layer was changed. (Manufacturing of Adhesive Layer) A styrene-based elastomer (manufactured by Asahi Kasei Chemicals: TAFTEC H1221, stupid ethylene copolymerization ratio of 12 wt%, MFR: 4.5 g/) was used in a 40 mm φ single-axis extruder. 10 min), melted by mixing 3.2 parts by weight of petroleum resin (manufactured by Arakawa Chemical Industry Co., Ltd.: Arkon P 1 25) and 3.2 parts by weight of polypropylene resin (manufactured by Sumitomo Chemical Co., Ltd.: FS201 1DG3, MFR: 2.5 g/10 min) Out as an adhesive layer. [Example 4] The base material layer and the release layer were maintained in the same manner as in Example 1. The adhesive layer was changed to the following, and three kinds of three-layer unstretched films were obtained by the same method as in Example 1. (Manufacturing of Adhesive Layer) Using a 40 mm φ single-axis extruder, 10 parts by weight of styrene-baked elastomer (Asahi Kasei Chemicals: TAFTEC H1221, this ethylene copolymerization ratio of 12 wt%, M FR) · 4_5g/l〇min), mixed with 8.8 parts by weight of petroleum resin (Arkon P125 manufactured by Arakawa Chemical Industry Co., Ltd.) and 8.8 parts by weight of polypropylene resin (manufactured by Sumitomo Chemical Co., Ltd.: WF83 6DG3, MFR: 7.0 g/10 min) The smelt is extruded and used as an adhesive layer. [Example 5] The release layer was maintained in the same manner as in Example 1. The base layer and the pressure-sensitive adhesive layer were changed to the following contents, and three kinds of three-layer unstretched films were obtained by the same method as in Example 1.

-22- S 201231609 (黏著層的製造) 使用40mm φ單軸擠出機將相對於ι〇〇重量份之苯乙 稀系彈性體(Asahi Kasei Chemicals 製:TAFTEC H1221 、苯乙烯共聚合比12wt%、MFR : 4.5g/l〇min),混合5.7 重量份之石油樹脂(荒川化學工業製:Arkon P125)及8.0 重量份之聚丙稀系樹脂(住友化學製:FS20 1 1 DG3、MFR :2.5g/10min)而成者熔融擠出而作為黏著層。 (基材層的製造) 使用90mm φ單軸擠出機將i〇〇wt〇/0之同元聚丙稀系 樹脂(住友化學製:FLX80E4(MFR : 7.5g/10min)熔融擠出 而成爲基材層。 [比較例1 ] 基材層、脫模層係維持與實施例1相同,將黏著層變 更為下述内容且使用與實施例丨同樣的製法而得到3種3 層的未延伸薄膜。 (黏著層的製造) 使用40mm φ單轴擠出機將相對於100重量份之苯乙 烯系彈性體(Asahi Kasei Chemicals 製:TAFTEC H1221 本乙細共聚合比12wt%、MFR : 4.5 g/1 Omin),混合1 7.6 重里份之石油樹脂(荒川化學工業製:Arkon P125)而成者 炫融擠出而作為黏著層。 [比較例2 ] 基材層、脫模層係維持與實施例丨相同,將黏著層變 更為下述内容且使用與實施例1同樣的製法而得到3種3 層的未延伸薄膜。 3 -23- .201231609 (黏著層的製造) 使用40mm φ單轴擠出機將相對於1〇〇重量份之苯乙 烯系彈性體(Asahi Kasei Chemicals 製:TAFTEC H1221 、苯乙稀共聚合比12wt%、MFR: 4.5g/1〇min),混合21 4 重量份之石油樹脂(荒川化學工業製:Ark〇nP125)及21 4 重量份之聚丙稀系樹脂(住友化學製:FS2〇1 1DG3、mfr ·· 2.5g/10min)而成者熔融擠出而作為黏著層。 [比較例3 ] 基材層、脫模層係維持與實施例1相同,將黏著層變 更為下述内容且使用與實施例丨同樣的製法而得到3種3 層的未延伸薄膜。 (黏著層的製造) 使用40mm φ單軸擠出機將相對於1〇〇重量份之苯乙 埽系彈性體(Asahi Kasei Chemicals 製:TAFTEC H1221 、笨乙烯共聚合比12wt%、MFR : 4.5g/10min),混合17·6 重置份之聚丙稀系樹脂(住友化學製:FS2〇llDG3、MFR .2.5 g/1 0 min)而成者熔融擠出而作為黏著層。 [比較例4] 脫模層係維持與實施例1相同,將黏著層、基材層變 更為下述内容且使用與實施例1同樣的製法而得到3種3 層的未延伸薄膜。 (霉占著層的製造) 使用40mm φ單軸擠出機將相對於1〇〇重量份之苯乙 埽系彈性體(Asahi Kasei Chemicals 製:TAFTEC H1221 、笨乙烯共聚合比12wt%、MFR : 4.5g/10min),混合17.6-22-S 201231609 (Manufacture of Adhesive Layer) A styrene-based elastomer (available from Asahi Kasei Chemicals: TAFTEC H1221, styrene copolymerization ratio: 12% by weight) using a 40 mm φ single-axis extruder MFR: 4.5 g/l〇min), 5.7 parts by weight of petroleum resin (Arkon P125 manufactured by Arakawa Chemical Industry Co., Ltd.) and 8.0 parts by weight of polypropylene resin (made by Sumitomo Chemical Co., Ltd.: FS20 1 1 DG3, MFR: 2.5 g) /10 min) The original is melt extruded and used as an adhesive layer. (Production of base material layer) A homopolymer polypropylene resin (manufactured by Sumitomo Chemical Co., Ltd.: FLX80E4 (MFR: 7.5 g/10 min) was melt-extruded to a base using a 90 mm φ single-axis extruder. [Comparative Example 1] The base material layer and the release layer were maintained in the same manner as in Example 1, and the adhesive layer was changed to the following contents, and three kinds of three-layer unstretched films were obtained by the same method as in Example 丨. (Manufacture of Adhesive Layer) Using a 40 mm φ single-axis extruder, 100 parts by weight of a styrene-based elastomer (manufactured by Asahi Kasei Chemicals: TAFTEC H1221, a copolymerization ratio of 12 wt%, MFR: 4.5 g/1) Omin), a mixture of 1 7.6 parts by weight of petroleum resin (Arkon P125 manufactured by Arakawa Chemical Industries Co., Ltd.) was used as an adhesive layer. [Comparative Example 2] Base material layer and release layer system were maintained and examples丨Similarly, the adhesive layer was changed to the following, and three kinds of three-layer unstretched films were obtained by the same method as in Example 1. 3-23-.201231609 (Manufacture of adhesive layer) Using a 40 mm φ single-axis extruder A styrene-based elastomer (manufactured by Asahi Kasei Chemicals) in an amount of 1 part by weight TAFTEC H1221, styrene copolymerization ratio 12wt%, MFR: 4.5g/1〇min), 21 4 parts by weight of petroleum resin (Ark〇nP125 manufactured by Arakawa Chemical Industry Co., Ltd.) and 21 4 parts by weight of polypropylene resin (manufactured by Sumitomo Chemical Co., Ltd.: FS2〇1 1DG3, mfr··2.5 g/10 min) The resultant was melt-extruded to form an adhesive layer. [Comparative Example 3] The base material layer and the release layer were maintained in the same manner as in Example 1, and The adhesive layer was changed to the following, and three kinds of three-layer unstretched films were obtained by the same method as in Example ( (manufacture of adhesive layer) Using a 40 mm φ single-axis extruder for 1 part by weight A styrene-based elastomer (manufactured by Asahi Kasei Chemicals: TAFTEC H1221, stupid ethylene copolymerization ratio: 12 wt%, MFR: 4.5 g/10 min), mixed with 17.6 replacement parts of polypropylene resin (manufactured by Sumitomo Chemical Co., Ltd.: FS2〇) llDG3, MFR .2.5 g/10 min) was melt-extruded as an adhesive layer. [Comparative Example 4] The release layer was maintained in the same manner as in Example 1, and the adhesive layer and the substrate layer were changed to the following contents. Three kinds of three-layer unstretched films were obtained by the same method as in Example 1. (Mold in the production of the layer) Single screw extruder with a 40mm φ 1〇〇 parts by weight with respect to the broom styrene-based elastomer (Asahi Kasei Chemicals Ltd.: TAFTEC H1221, stupid ethylene copolymerization ratio 12wt%, MFR: 4.5g / 10min), mix 17.6

S -24- 201231609 重量份之石油樹脂(荒川化學工業製:Arkon P 125)而成者 熔融擠出而作為黏著層。 (基材層的製造) 使用90mm φ單轴擠出機將100〜〇/〇之同元聚丙稀系 樹脂(住友化學製:FLX80E4(MFR : 7.5g/10min)熔融擠出 而成為基材層。 [比較例5 ] 基材層、脫模層係維持與實施例1相同,將黏著層變 更為下述内容且使用與實施例丨同樣的製法而得到3種3 層的未延伸薄膜。 (黏著層的製造) 使用40mm φ單轴擠出機將相對於100重量份之笨乙 烯系彈性體(Asahi Kasei Chemicals製:TAFTEC H1221 、苯乙烯共聚合比12wt%、MFR : 4.5g/10min),混合6.4 重量份之石油樹脂(荒川化學工業製:Arkon P125)而成者 熔融擠出而作為黏著層。 [比較例6] 基材層、脫模層係維持與實施例1相同,將黏著層變 更為下述内容且使用與實施例1同樣的製法而得到3種3 層的未延伸薄膜。 (點著層的製造) 使用40mm φ單軸擠出機將相對於1〇〇重量份之苯乙 埽系彈性體(Asahi Kasei Chemicals 製:TAFTEC H1221 本乙稀共聚合比12wt% ' MFR : 4.5g/10min),混合6.3 重量份之石油樹脂(荒川化學工業製:Arkon P 125)及18.8S -24- 201231609 Part by weight of petroleum resin (manufactured by Arakawa Chemical Industry Co., Ltd.: Arkon P 125). It is melt-extruded and used as an adhesive layer. (Production of base material layer) 100 to 〇/〇 of the homopolymer polypropylene resin (manufactured by Sumitomo Chemical Co., Ltd.: FLX80E4 (MFR: 7.5 g/10 min) was melt-extruded to form a substrate layer using a 90 mm φ single-axis extruder. [Comparative Example 5] The base material layer and the release layer were maintained in the same manner as in Example 1. The adhesive layer was changed to the following contents, and three kinds of three-layer unstretched films were obtained by the same method as in Example 。. Production of Adhesive Layer) Using a 40 mm φ single-axis extruder, 100 parts by weight of a stupid vinyl elastomer (TAATEC Kasei Chemicals: TAFTEC H1221, styrene copolymerization ratio: 12 wt%, MFR: 4.5 g/10 min) was used. 6.4 parts by weight of petroleum resin (Arkon P125, manufactured by Arakawa Chemical Industry Co., Ltd.) was mixed and melt-extruded to form an adhesive layer. [Comparative Example 6] The base material layer and the release layer were maintained in the same manner as in Example 1, and the adhesive layer was adhered. Three types of three-layer unstretched films were obtained by the same method as in Example 1 by changing the following contents. (Production of the dot layer) Using a 40 mm φ single-axis extruder to measure benzene relative to 1 part by weight Ethylene elastomer (made by Asahi Kasei Chemicals: TAFTEC H1221) Polymerization than 12wt% 'MFR: 4.5g / 10min), mix 6.3 parts by weight of a petroleum resin (Arakawa Chemical Industries, Ltd.: Arkon P 125) and 18.8

-25- S 201231609-25- S 201231609

重量份之聚丙烯系樹脂(住友化學製:FS2011DG3、MFR .2.5g/l〇min;)而成者熔融擠出而作為黏著層。 [比較例7] 土材層脫模層係維持與實施例1相同,將黏著層變 為下述内谷且使用與實施例丨同樣的製法而得到3種3 層的未延伸薄膜。 (黏著層的製造) 使用40mm φ單軸擠出機將相對於1〇〇重量份之苯乙 稀系彈性體(Asahi Kasei Chemicals 製:TAFTEC H1221 、苯乙烯共聚合比12wt%、MFR : 4.5g/l〇min),混合18.8 重®份之石油樹脂(荒川化學工業製:Ark〇n pi25)&6 3 重里伤之聚丙烯系樹脂(住友化學製:WF836dG3、MFR .7.0g/10min)而成者熔融擠出而作為黏著層。 [比較例8] 基材層、脫模層係維持與實施例1相同,將黏著層變 更為下述内容且使用與實施例1同樣的製法而得到3種3 層的未延伸薄膜。 (等占著層的製造) 使用40mm φ單軸擠出機將相對於1〇〇重量份之苯乙 缚系彈性體(Asahi Kasei Chemicals 製:TAFTEC H1062 、笨乙烯共聚合比18wt% ' MFR : 4,5g/10min),混合8.8 重量份之石油樹脂(荒川化學工業製:Arkon P 125)及8.8 重量份之聚丙烯系樹脂(住友化學製:Fs20 11DG3、MFR :2.5g/10min)而成者熔融擠出而作為黏著層。 將上述結果顯示在表1、2、3。 201231609A part by weight of a polypropylene resin (manufactured by Sumitomo Chemical Co., Ltd.: FS2011DG3, MFR, 2.5 g/l〇min;) was melt-extruded to form an adhesive layer. [Comparative Example 7] The soil layer release layer was maintained in the same manner as in Example 1. The adhesive layer was changed to the following inner valley, and three types of three-layer unstretched films were obtained by the same method as in Example 。. (Manufacture of Adhesive Layer) A styrene-based elastomer (manufactured by Asahi Kasei Chemicals: TAFTEC H1221, styrene copolymerization ratio: 12 wt%, MFR: 4.5 g) was used in a 40 mm φ single-axis extruder. /l〇min), a mixture of 18.8 parts by weight of petroleum resin (Ark〇n pi25 manufactured by Arakawa Chemical Industry Co., Ltd.) & 6 3 Polypropylene resin (made by Sumitomo Chemical Co., Ltd.: WF836dG3, MFR.7.0g/10min) The original is melt extruded and used as an adhesive layer. [Comparative Example 8] The base material layer and the release layer were maintained in the same manner as in Example 1. The adhesive layer was changed to the following, and three kinds of three-layer unstretched films were obtained by the same method as in Example 1. (Equivalent to the manufacture of the layer) Using a 40 mm φ single-axis extruder, 1 part by weight of the styrene-based elastomer (manufactured by Asahi Kasei Chemicals: TAFTEC H1062, stupid ethylene copolymerization ratio 18 wt% 'MFR: 4,5 g/10 min), 8.8 parts by weight of petroleum resin (Arkon P 125 manufactured by Arakawa Chemical Industry Co., Ltd.) and 8.8 parts by weight of polypropylene resin (manufactured by Sumitomo Chemical Co., Ltd.: Fs20 11DG3, MFR: 2.5 g/10 min) The melt is extruded and used as an adhesive layer. The above results are shown in Tables 1, 2 and 3. 201231609

【I FS2011 DG3 oo 卜 FLX80E4 ο t-H BC4FC ο ν〇 oo ν〇 oo 〇\ § 寸 0.577 〇 Arkon P125 卜 in TAFTEC H1221 〇 t i oo oo 寸 WF836 DG3 OO oo in FS2011DG3 Ο ο BC4FC ο 1—Η Ο oo Ο in Os <N 710 ON v〇 VO v〇 0.588 〇 Arkon P125 oo oo TAFTEC H1221 o ^Τϊ 00 CO FS2011 DG3 CN rn m FS2011DG3 ο ο τ—Η BC4FC ο ψ 4 Ό oo ν〇 00 On (S 660 (N 寸 o 0.581 〇 Arkon P125 <N cn ro TAFTEC H1221 o r-H CN 军 Arkon|FS2011 P125 1 DG3 OO OO 00 oo <〇 FLX80E4 Ο BC4FC Ο ί-Η Ό 00 ν〇 00 OS v〇 730 r- o 0.592 〇 TAFTEC H1221 o ό oo —_Η s •VC? FS2011 DG3 oo oo FS2011DG3 Ο ο BC4FC Ο 00 ν〇 G\ oo 720 On 卜 s 0.588 〇 Arkon P125 00 oo TAFTEC H1221 o oo 1 重量份 重量% 重量% 1重量% ι μΐΏ ε ε cN/25mm cN/25mm cN/25mm cN/25nun 1 原料名 調配量 調配比 原料名I 調配量 1原料名ι 調配量 1黏著層ι 1基材層I 脫模層 1黏著層ι 1黏著層i l壓克力板I I棱鏡片11 |稜鏡片2| 脫模層 脫模層 操作性 黏著層 基材層 脫模層 層結構 l延展率ι 1裹包率ι 黏著力 |剝離力1 平均表面 粗極度SRa _ Ll, s 201231609 【(N<】 比較例4 FLX80E4 Ο BC4FC Ο ν〇 00 ο 00 οο m m 750 v〇 (N CN <N » < 0.585 〇 Arkon P125 17.6 ID TAFTEC H1221 Ο οο 比較例3 FS2011DG3 ο 1 ( BC4FC Ο ο οο ν〇 〇\ o 〇 Ο (N 0.574 〇 FS2011 DG3 17.6 TAFTEC H1221 Ο Η wo 00 比較例2 FS2011 DG3 21.4 FS2011DG3 ο ψ · Η BC4FC Ο <〇 οο ν〇 σ\ 00 CO in m 〇 ο in 0.594 X :Arkon ;P125 21.4 νο Τ"·^ TAFTEC H1221 ο ο 比較例1 FS2011DG3 ο BC4FC ο οο ΙΓ) οο rn 卜 0.563 〇 Arkon :P125 17.6 TAFTEC HI 221 Ο οο 1 重量份 重量% ι 重量% 1重量% ι μυΐ ε ε cN/25mm cN/25mm cN/25mm cN/25mm 1 原料名 調配量 調配比 原料名 調配量 原料名 調配量 黏著層 基材層 脫模層 1黏著層 黏著層 壓克力板 稜鏡片1 棱鏡片2 脫模層 脫模層 操作性 黏著層 基材層 脫模層 層結構 1延展率ι 裹包率 黏著力 剝離力 平均表面 粗糖度SRa -OOCN· c 201231609 比較例8 FS2011 ! DG3 00 〇6 FS2011DG3 Ο BC4FC Ο ^Η Ό 00 VO «η a\ σ\ 420 ο ο 0.583 X Arkon P125 oo od TAFTEC H1221 〇 1 < 00 比較例7 FS2011 DG3 CO FS2011DG3 Ο BC4FC Ο Ό oo VO v〇 oo ΓΛ ir> CO ro ίΝ σ\ Η r-H 0.577 〇 Arkon P125 18.8 TAFTEC HI 221 o 1—H g 比較例6 FS2011 DG3 18.8 in i FS2011DG3 Ο BC4FC ο v〇 oo v〇 On CO m Ο ο 寸 0.581 X Arkon ! 1 P125 I uo TAFTEC H1221 〇 g 比較例5 FS2011DG3 ο » < BC4FC ο r-H Ό oo V£> oi 700 寸 0.591 〇 Arkon P125 寸 TAFTEC 1 H1221 o / 重量份 重量% 重量% 重量% a a n a zL |cN/25mm cN/25mm cN/25mm cN/25mm 1 調配量 調配比 原料名 調配量 原料名 調配量 黏著層 基材層 脫模層 黏著層 黏著層 壓克力板 稜鏡片1 稜鏡片2 脫模層 脫模層 操作性 黏著層 基材層 脫模層 層結構 延展率 1裹包率 黏著力 剝離力 平均表面 粗縫度SRa -6Ζ·s 201231609 從表1可以清楚明白,在實施例i〜5所得到之薄膜, 係薄膜製膜時的延展性良好且作為保護薄膜使用時具有 實用上充分的黏著力,而且使薄膜成為捲筒時之操作性 亦良好。 另一方面,比較例1、4及7所得到之薄膜,薄膜製膜 時之延展性為不充分,黏著劑產生裹包,係未必可說是 製膜性良好之結果。又,關於使薄膜成為捲筒時之搡作 f生,亦未必可說是良好之結果。比較例2、3、6及8所得 到之薄膜,在被覆體之稜鏡片上係不具有實用上必須的 黏著力之結果。比較例5所得到之薄膜,關於使薄膜成為 捲筒時之操作性,亦未必可說是良好之結果。如此,比 較例所得到的薄膜係任一者均是品質差且實用性低者。 [產業上之利用可能性] _ 本發明的黏著劑係特別適合使用於用以保護在光, 用途所使用之稜鏡片的稜型透鏡部的外表面之黏著薄膜 又,為了要保護合成樹脂板(例如建築 . :鋼板(例如建築材料用)、銘板、裝飾合板=、; .二:電製品、精密機械及製造時之汽車車體的表Θ 品避免;傷保存、輸送及製造步驟搬運時為了要保言“ 避免文傷,以及在二次加工 )時保護物品避免受傷之产、介处热* 和加壓加^ 的貢獻重大/免又知之清況亦此夠適合使用’對產" 【圖式簡單說明】 第1圖係測定試料的模式圖。 【主要元件符號說明】 jfe 〇 <%«、[I FS2011 DG3 oo 卜 FLX80E4 ο tH BC4FC ο ν〇oo ν〇oo 〇 \ § inch 0.577 〇Arkon P125 卜 in TAFTEC H1221 〇ti oo oo inch WF836 DG3 OO oo in FS2011DG3 Ο ο BC4FC ο 1—Η Ο oo Ο In os lt kon 88 88 88 88 88 N inch o 0.581 〇Arkon P125 <N cn ro TAFTEC H1221 o rH CN Army Arkon|FS2011 P125 1 DG3 OO OO 00 oo <〇FLX80E4 Ο BC4FC Ο ί-Η Ό 00 ν〇00 OS v〇730 r- o 0.592 〇TAFTEC H1221 o ό oo —_Η s •VC? FS2011 DG3 oo oo FS2011DG3 Ο ο BC4FC Ο 00 ν〇G\ oo 720 On 卜 s 0.588 〇Arkon P125 00 oo TAFTEC H1221 o oo 1 parts by weight % by weight % 1 Weight % ι μΐΏ ε ε cN/25mm cN/25mm cN/25mm cN/25nun 1 Raw material name blending ratio Raw material name I Formulation amount 1 Raw material name ι Formulation amount 1 Adhesive layer ι 1 Substrate layer I Release layer 1 Adhesive Layer ι 1 adhesive layer il acrylic plate II prism sheet 11 | 稜鏡 2 2| Release layer release layer operative adhesive layer base layer release layer structure l elongation rate ι 1 wrapping ratio ι adhesion|peeling force 1 average surface roughness extreme SRa _ Ll, s 201231609 [(N<] Comparative Example 4 FX4E Ο BC 00 〇Ο (N 0.574 〇FS2011 DG3 17.6 TAFTEC H1221 Ο Η wo 00 Comparative Example 2 FS2011 DG3 21.4 FS2011DG3 ο ψ · Η BC4FC Ο <〇οο ν〇σ\ 00 CO in m 〇ο in 0.594 X : Arkon ;P125 21.4 νοΤ"·^ TAFTEC H1221 ο ο Comparative Example 1 FS2011DG3 ο BC4FC ο οο ΙΓ) οο rn 卜 0.563 〇Arkon :P125 17.6 TAFTEC HI 221 Ο οο 1 Parts by weight % ι % by weight 1% by weight ι μυΐ ε ε cN/ 25mm cN/25mm cN/25mm cN/25mm 1 Raw material name blending ratio Raw material name blending amount Raw material name blending amount Adhesive layer base layer Release layer 1 Adhesive layer Adhesive laminated Kelly plate sheet 1 Prism sheet 2 Stripping Release layer operative adhesive layer base layer release layer structure 1 elongation rate ι wrapping ratio adhesion peeling force average surface roughness saccharide SRa - OOCN · c 201231609 Comparative Example 8 FS2011 ! DG3 00 〇6 FS2011DG3 Ο BC4FC Ο ^ Η 00 00 VO «η a\ σ\ 420 ο ο 0.583 X Arkon P125 oo od TAFTEC H1221 〇1 < 00 Comparative Example 7 FS2011 DG3 CO FS2011DG3 BC BC4FC Ο oo oo VO v〇oo ΓΛ ir> CO ro ίΝ σ\ Η rH 0.577 〇Arkon P125 18.8 TAFTEC HI 221 o 1—H g Comparative Example 6 FS2011 DG3 18.8 in i FS2011DG3 Ο BC4FC ο v〇oo v〇On CO m Ο ο 寸 0.581 X Arkon ! 1 P125 I uo TAFTEC H1221 〇g Comparative Example 5 FS2011DG3 ο » < BC4FC ο rH Ό oo V£> oi 700 inch 0.591 〇Arkon P125 inch TAFTEC 1 H1221 o / parts by weight % by weight % by weight aana zL |cN/25mm cN/25mm cN/25mm cN/25mm 1 compounding quantity ratio raw material name compounding quantity raw material name matching amount adhesive layer base layer release layer adhesive layer adhesion laminated kelly sheet 1 piece 2 release layer release layer operative adhesive layer substrate Layer release layer structure elongation rate 1 wrap ratio adhesive force peeling force average surface rough seam degree SRa -6 Ζ·s 201231609 It can be clearly seen from Table 1 that the films obtained in Examples i to 5 are film-forming films. It has good ductility and has a practically sufficient adhesive force when used as a protective film, and also has good handleability when the film is formed into a roll. On the other hand, in the films obtained in Comparative Examples 1, 4 and 7, the ductility at the time of film formation was insufficient, and the adhesive was wrapped, which was not necessarily a result of good film formability. Further, it is not necessarily a good result as to make the film into a roll. The films obtained in Comparative Examples 2, 3, 6 and 8 did not have the practically necessary adhesive force on the crepe of the covering. The film obtained in Comparative Example 5 was not necessarily a good result with respect to the workability when the film was formed into a roll. Thus, any of the film systems obtained in the comparative examples was inferior in quality and low in practicality. [Industrial Applicability] _ The adhesive of the present invention is particularly suitable for use in an adhesive film for protecting the outer surface of a prismatic lens portion of a ruthenium used for light and use, in order to protect a synthetic resin sheet. (eg construction. : steel plates (for example for building materials), nameplates, decorative plywoods =, ; . 2: electrical products, precision machinery and the appearance of the car body during manufacture; avoidance; preservation, transport and manufacturing steps In order to protect the article from "in case of literary injury and secondary processing", it is important to protect the goods from injury, the heat* and the pressure plus ^. [Simplified description of the drawing] Fig. 1 is a schematic diagram of the measurement sample. [Description of main component symbols] jfe 〇<%«,

S -30-S -30-

Claims (1)

201231609 七、申請專利範圍: 1 一種黏著性樹脂組成物’其特徵在於包含: 含有相對於100重量份之苯乙烯系彈性體,含有2 重量份以上小於1 〇重量份的黏著賦予樹脂、2重量份以 上小於1 0重量份的聚烯烴系樹脂之樹脂組成物; 該苯乙烯系彈性體係苯乙烯成分為5〜丨5重量%,並 且將本乙稀系聚合物敌段與稀烴系聚合物嵌段的參段 共聚物、苯乙烯系聚合物嵌段及苯乙烯與烯烴的無規 共聚物嵌段之嵌段共聚物、及/或該等的氫化物作為主 成分。 2.—種黏著薄膜,其特徵在於: 在將聚丙烯系樹脂作為主成分之基材層的一面上 積層如申請專利範圍第1項之黏著性樹脂組成物而成。 3 ·如申請專利範圍第2項之黏著薄膜,其係在將聚丙烯系 樹脂作為主成分的基材層之與包含黏著性樹脂組成物 之黏著層相反的面上,與脫模層積層而成。 4 _如申請專利範圍第3項之黏著薄膜,其係藉由共擠出將 聚丙烯系樹脂作為主成分的基材層、包含黏著性樹脂 組成物之黏著層、脫模層積層而成。 5. 如申請專利範圍第2至4項中任一項之黏著薄膜,其令 該黏著層中的笨乙烯系彈性體在23(TC、2.1 6kgf之熔融 流速(melt flow rate ; MFR)為 〇.5~10g/10 分鐘。 6. 如申請專利範圍第2至5項中任一項之黏著薄膜,其中 該基材層中的聚丙烯系樹脂在230°C、2.16kgf之熔融流 速(melt flow rate ; MFR)為 i.o 〜i5g/10 分鐘。 E -31- 201231609 7 ·如申請專利範圍第2至6項中任一項之黏著薄膜,其係 棱鏡片被覆用。 8.如申請專利範圍第2至7項中任一項之黏著薄膜,其係 自身黏著性。 -32-201231609 VII. Patent Application Range: 1 An adhesive resin composition characterized by comprising: an adhesive-imparting resin containing 2 parts by weight or more and less than 1 part by weight, based on 100 parts by weight of the styrene-based elastomer, 2 parts by weight a resin composition of less than 10 parts by weight of a polyolefin-based resin; the styrene-based elastomeric system has a styrene component of 5 to 5% by weight, and the ethylenic polymer enemy group and the dilute hydrocarbon polymer The block copolymer of the block, the styrene polymer block, and the block copolymer of the random copolymer block of styrene and olefin, and/or the hydride are the main components. 2. An adhesive film comprising: an adhesive resin composition according to claim 1 of the patent application, laminated on one surface of a base material layer containing a polypropylene resin as a main component. 3. The adhesive film of claim 2, wherein the base material layer containing the polypropylene resin as a main component is laminated on the surface opposite to the adhesive layer containing the adhesive resin composition, and the release layer is laminated. to make. (4) The adhesive film of claim 3, which is obtained by coextruding a base material layer containing a polypropylene resin as a main component, an adhesive layer containing an adhesive resin composition, and a release layer. 5. The adhesive film according to any one of claims 2 to 4, wherein the stray ethylene-based elastomer in the adhesive layer has a melt flow rate (MFR) of 23 (TC, 2.1 6 kgf). The adhesive film according to any one of claims 2 to 5, wherein the polypropylene resin in the substrate layer has a melt flow rate of 2.16 kgf at 230 ° C (melt) The flow rate; MFR) is io ~ i5g / 10 minutes. E -31 - 201231609 7 - The adhesive film according to any one of claims 2 to 6, which is coated with a prism sheet. Adhesive film according to any one of items 2 to 7, which is self-adhesive. -32-
TW100143855A 2010-12-01 2011-11-30 Adhesive and adhesive film TWI443172B (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP2010268525 2010-12-01
JP2011238933A JP5987293B2 (en) 2010-12-01 2011-10-31 Adhesive and adhesive film

Publications (2)

Publication Number Publication Date
TW201231609A true TW201231609A (en) 2012-08-01
TWI443172B TWI443172B (en) 2014-07-01

Family

ID=46171908

Family Applications (1)

Application Number Title Priority Date Filing Date
TW100143855A TWI443172B (en) 2010-12-01 2011-11-30 Adhesive and adhesive film

Country Status (5)

Country Link
JP (1) JP5987293B2 (en)
KR (1) KR101867113B1 (en)
CN (1) CN103261352B (en)
TW (1) TWI443172B (en)
WO (1) WO2012073979A1 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
TWI607945B (en) * 2012-10-05 2017-12-11 東洋紡股份有限公司 Self-adhesive surface protection film

Families Citing this family (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2016196650A (en) * 2010-12-01 2016-11-24 東洋紡株式会社 Adhesive and adhesive film
KR102089231B1 (en) * 2012-04-10 2020-03-13 도요보 가부시키가이샤 Self-adhesive surface protection film
JP6506556B2 (en) * 2012-10-05 2019-04-24 東洋紡株式会社 Self-adhesive surface protection film
JP6323690B2 (en) * 2013-04-11 2018-05-16 東洋紡株式会社 Self-adhesive surface protective film
JP6515917B2 (en) * 2014-06-18 2019-05-22 東洋紡株式会社 Self-adhesive surface protection film
WO2016063673A1 (en) * 2014-10-20 2016-04-28 東レフィルム加工株式会社 Composition and laminate
JP2016183241A (en) * 2015-03-26 2016-10-20 株式会社サンエー化研 Adhesive composition, and adhesive film and surface protection sheet using the same
CN107573862B (en) * 2017-08-21 2021-06-22 张家港康得新光电材料有限公司 Adhesive resin composition and self-adhesive protective film
JP7188672B2 (en) * 2018-04-16 2022-12-13 東レフィルム加工株式会社 laminated film
WO2023234208A1 (en) * 2022-05-31 2023-12-07 日東電工株式会社 Adhesive sheet

Family Cites Families (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2713519B2 (en) * 1991-01-31 1998-02-16 積水化学工業株式会社 Surface protection film
JPH10151656A (en) 1996-11-22 1998-06-09 Sekisui Chem Co Ltd Manufacture of surface protective film
JP4979846B2 (en) * 2000-12-04 2012-07-18 日東電工株式会社 Method for producing adhesive film
JP2002285116A (en) * 2001-03-26 2002-10-03 Nitto Denko Corp Surface protecting sheet and method for producing the same
JP4115791B2 (en) * 2002-03-05 2008-07-09 日東電工株式会社 Surface protection sheet
CN101189317A (en) * 2005-06-06 2008-05-28 积水化学工业株式会社 Surface protective film
WO2006132183A1 (en) * 2005-06-06 2006-12-14 Sekisui Chemical Co., Ltd. Surface protection film
JP4693599B2 (en) * 2005-11-04 2011-06-01 積水化学工業株式会社 Method for producing surface protective film
JP4987361B2 (en) 2006-06-19 2012-07-25 積水化学工業株式会社 Surface protection film
JP2008127447A (en) * 2006-11-20 2008-06-05 Sekisui Chem Co Ltd Surface protection film
JP5288733B2 (en) * 2007-05-31 2013-09-11 出光ユニテック株式会社 Surface protection film
JP5446369B2 (en) * 2008-04-30 2014-03-19 東洋紡株式会社 Adhesive film
JP5503129B2 (en) * 2008-09-29 2014-05-28 積水化学工業株式会社 Masking tape and manufacturing method thereof
JP5280902B2 (en) * 2009-03-18 2013-09-04 積水化学工業株式会社 Surface protection sheet for prism sheet

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
TWI607945B (en) * 2012-10-05 2017-12-11 東洋紡股份有限公司 Self-adhesive surface protection film

Also Published As

Publication number Publication date
CN103261352A (en) 2013-08-21
JP2012131978A (en) 2012-07-12
CN103261352B (en) 2016-01-27
KR101867113B1 (en) 2018-06-12
WO2012073979A1 (en) 2012-06-07
JP5987293B2 (en) 2016-09-07
KR20130129210A (en) 2013-11-27
TWI443172B (en) 2014-07-01

Similar Documents

Publication Publication Date Title
TW201231609A (en) Adhesive and adhesive film
JP6569723B2 (en) Self-adhesive surface protective film
JP5446369B2 (en) Adhesive film
TWI565590B (en) Polyolefin based film
TWI555808B (en) Polyolefin based film
TWI600739B (en) Self-adhesive surface protection film
TWI621683B (en) Self-adhesive surface protection film
JP5445023B2 (en) Adhesive film
KR20140022005A (en) Surface-protecting film
JP2018127637A (en) Self-adhesive surface protective film
JP6515917B2 (en) Self-adhesive surface protection film
TW201136951A (en) Surface protective film
JP2016196650A (en) Adhesive and adhesive film
JP2009287005A (en) Adhesive film
JP5445022B2 (en) Adhesive film

Legal Events

Date Code Title Description
MM4A Annulment or lapse of patent due to non-payment of fees