TW201222930A - A laminated material for secondary battery container and method for manufacturing the same and secondary battery container - Google Patents

A laminated material for secondary battery container and method for manufacturing the same and secondary battery container Download PDF

Info

Publication number
TW201222930A
TW201222930A TW100120629A TW100120629A TW201222930A TW 201222930 A TW201222930 A TW 201222930A TW 100120629 A TW100120629 A TW 100120629A TW 100120629 A TW100120629 A TW 100120629A TW 201222930 A TW201222930 A TW 201222930A
Authority
TW
Taiwan
Prior art keywords
film
pet pet
laminate
mpa
modified
Prior art date
Application number
TW100120629A
Other languages
Chinese (zh)
Inventor
Yasushi Tateishi
Satoshi Ishii
Masaaki Ono
Ken Ota
Hiroshi Tougou
Toru Miyake
Original Assignee
Toray Advanced Film Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Toray Advanced Film Co Ltd filed Critical Toray Advanced Film Co Ltd
Publication of TW201222930A publication Critical patent/TW201222930A/en

Links

Classifications

    • 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
    • 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
    • B32B15/00Layered products comprising a layer of metal
    • B32B15/04Layered products comprising a layer of metal comprising metal as the main or only constituent of a layer, which is next to another layer of the same or of a different material
    • B32B15/08Layered products comprising a layer of metal comprising metal 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
    • B32B15/082Layered products comprising a layer of metal comprising metal 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 comprising vinyl resins; comprising acrylic resins
    • 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
    • B32B15/00Layered products comprising a layer of metal
    • B32B15/04Layered products comprising a layer of metal comprising metal as the main or only constituent of a layer, which is next to another layer of the same or of a different material
    • B32B15/08Layered products comprising a layer of metal comprising metal 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
    • B32B15/085Layered products comprising a layer of metal comprising metal 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 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
    • B32B15/00Layered products comprising a layer of metal
    • B32B15/04Layered products comprising a layer of metal comprising metal as the main or only constituent of a layer, which is next to another layer of the same or of a different material
    • B32B15/08Layered products comprising a layer of metal comprising metal 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
    • B32B15/088Layered products comprising a layer of metal comprising metal 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 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
    • B32B15/00Layered products comprising a layer of metal
    • B32B15/20Layered products comprising a layer of metal comprising aluminium or copper
    • 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
    • B32B27/30Layered products comprising a layer of synthetic resin comprising vinyl (co)polymers; comprising acrylic (co)polymers
    • B32B27/306Layered products comprising a layer of synthetic resin comprising vinyl (co)polymers; comprising acrylic (co)polymers comprising vinyl acetate or vinyl alcohol (co)polymers
    • 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
    • B32B27/30Layered products comprising a layer of synthetic resin comprising vinyl (co)polymers; comprising acrylic (co)polymers
    • B32B27/308Layered products comprising a layer of synthetic resin comprising vinyl (co)polymers; comprising acrylic (co)polymers comprising acrylic (co)polymers
    • 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
    • B32B27/34Layered 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
    • B32B27/36Layered products comprising a layer of synthetic resin comprising polyesters
    • 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
    • B32B2250/055 or more layers
    • 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
    • B32B2255/00Coating on the layer surface
    • B32B2255/10Coating on the layer surface on synthetic resin layer or on natural or synthetic rubber layer
    • 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
    • B32B2255/00Coating on the layer surface
    • B32B2255/26Polymeric coating
    • 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
    • B32B2307/514Oriented
    • B32B2307/518Oriented bi-axially
    • 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
    • B32B2307/54Yield strength; Tensile strength
    • 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
    • B32B2307/558Impact strength, toughness
    • 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
    • B32B2307/714Inert, i.e. inert to chemical degradation, corrosion
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M50/00Constructional details or processes of manufacture of the non-active parts of electrochemical cells other than fuel cells, e.g. hybrid cells
    • H01M50/10Primary casings; Jackets or wrappings
    • H01M50/116Primary casings; Jackets or wrappings characterised by the material
    • H01M50/124Primary casings; Jackets or wrappings characterised by the material having a layered structure
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M50/00Constructional details or processes of manufacture of the non-active parts of electrochemical cells other than fuel cells, e.g. hybrid cells
    • H01M50/10Primary casings; Jackets or wrappings
    • H01M50/116Primary casings; Jackets or wrappings characterised by the material
    • H01M50/124Primary casings; Jackets or wrappings characterised by the material having a layered structure
    • H01M50/1245Primary casings; Jackets or wrappings characterised by the material having a layered structure characterised by the external coating on the casing
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02EREDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E60/00Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
    • Y02E60/10Energy storage using batteries

Landscapes

  • Sealing Battery Cases Or Jackets (AREA)
  • Laminated Bodies (AREA)

Abstract

The present invention provides a laminated material which can be used in secondary battery container or outer packing material having excellent vibration resistance and a secondary battery using the laminated material thereof. The laminated material is a laminated material formed by laminating a film (A) comprising polyethylene terephthalate, polyethylene naphthalate, poly lactic acid or para-aromatic polyamide, a nylon 6 film (B), a aluminum foil (C) and a polypropylene film (D) in turn, which is characterized in that: A is a biaxial orientation film, B and D are non-orientation films, a modified polyolefine layer set between C and D and the Young's modulus of D is under 500MPa.

Description

201222930 六、發明說明: 【舍明所屬之技術領域】 本發明關於二次雷β ’斤使用的積層材,古輩知而·^·, 關於作為二次電池的容 柯孑細而β 衝擊性優I t Μ # ° 裝材使用的耐振動性及耐 ,=優異之積層材與使用其 【先前技術】 电也用谷益。 促進電動汽車、';i 其中,鋰離子二3 正使用以鋁箔當f 以環境保護運動的高漲為背景 合動力汽車、電動二輪車等的導入 電池的利用係被認為前途有望。 於鐘離子二次電池用外襄材中 電池構造的積層材。作為 ^鋁“ q 女水的性能,可蠱+ 、火 氣透過性極低,(ii)内部電解 特性優異,經時後沒有内;脫=耐” (1搞壓成形,成形後…:現=7:離)等 形後在内層薄膜不發生裂紋 · S H⑺ .^ 冤池作成時引線與積声 中的鋁不導通’(vi)即使在u 曰 得住的耐熱性等。 乜八有暫時 作為滿足此專的積層材,提屮一 一 積層材(專利文獻1 ),苴俜積 人電池谷器 “ 積層有外裝樹脂薄膜/莖— 者劑層/化成處理鋁箔/第二黏著劑 、第 ”知丨k /也封薄膜之積; ’其特徵為:密封薄膜係由α_烯 積層 0/ ,, JS里馬2〜1〇番 /❶的丙稀肖α-烯烴之無規共聚物所構成, ’含有〜25,pm的…或油醒胺與為:。 250〇ppm的伸乙基雙油醯胺,—一 種-久電池交55 B9 1士 材(專利文獻2),其係積層有外穿 盗用積 卜裝枒脂溥膜/黏著劑層/ 201222930 成處理鋁猪/底漆層/密封薄膜之積層材,其特徵為·密 封薄膜係由α-烯烴的含量為2〜1〇重量%的丙烯與心烯 烴之無規共聚物、與2〜4〇重量%的彈性體或聚丁烯中 的任-種以上之摻合品’其含有〇 5%重量%以下的 ,而實用化等。 又,電子零件包裝用袋係為了防止受到靜電的破壞 或濕度的影響而品f降低之包裝用袋,在將電子零件收 納於袋内部時,電子零件的邊緣係強烈碰揸,以袋包裝 電子零件而移送之際,由於電子零件或外部的突起而容 易破袋,為了改善所謂的耐穿刺性,有提出—種電子零 件包裝用積層薄膜(專利文獻3)等,其係夾有金屬箔,在 側積層熱塑性樹脂層(A),而且在另一側積層熱塑性樹 脂層(B)而成之積層薄膜,金屬箔與熱塑性樹脂層係藉由 壓出積層而貼合,且以熱塑性樹脂層(A)的拉伸長強度為 Sa、以斷裂時的伸長度為Ea,以熱塑性樹脂層(b)的拉伸 強度為Sb,以斷裂時的伸長度為Eb時,上述熱塑性樹 脂層(A)及熱塑性樹脂層(B)具有拉伸強度的比為201222930 VI. Description of the invention: [Technical field to which the invention relates] The present invention relates to a laminated material used for a secondary thunder, which is known as the secondary battery, and has a β impact resistance as a secondary battery. Excellent I t Μ # ° Resistance to vibration and resistance of the material used, = Excellent laminate and its use [Prior Art] Electricity is also used in Gu Yi. In the case of the use of the battery, the use of the battery is considered to be promising. In the outer coffin for the ion secondary battery, the laminated material of the battery structure. As the performance of ^ aluminum "q female water, it can be 蛊+, the gas permeability is extremely low, (ii) the internal electrolytic characteristics are excellent, and there is no internal after the time; the off = resistance" (1 press forming, forming...: now = 7: After the isomorphism, the inner film does not crack. · S H(7) .^ When the cell is made, the lead and the aluminum in the sound are not turned on' (vi) heat resistance even in the case of u.乜 有 暂时 暂时 暂时 暂时 暂时 暂时 暂时 暂时 暂时 暂时 暂时 暂时 暂时 ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( Two adhesives, the first product of the "knowing k / also sealing film; 'characterized by: the sealing film is composed of α-ene layer 0 / , JS Lima 2~1 〇 / / 丙 肖 α α α olefin The random copolymer consists of 'containing ~25, pm... or oleoamine with: 250〇ppm of ethyl acenaphthylamine, a kind of long-term battery 55 B9 1 material (patent document 2), which has a layer of external wear and pirate, a blush film/adhesive layer / 201222930 A laminate for treating an aluminum pig/primer layer/sealing film, characterized in that the sealing film is a random copolymer of propylene and a heart olefin having an α-olefin content of 2 to 1% by weight, and 2 to 4 Å. The blend of any one or more of the weight % of the elastomer or the polybutene is contained in an amount of 5% by weight or less, and is put into practical use. In addition, the electronic component packaging bag is a packaging bag which is protected from the damage of static electricity or the influence of humidity, and when the electronic component is housed inside the bag, the edge of the electronic component is strongly touched, and the electronic component is packaged in a bag. When the parts are transferred, the electronic components or the external projections are likely to be broken, and in order to improve the puncture resistance, there is a laminated film for electronic component packaging (Patent Document 3), etc., which is provided with a metal foil. A laminated film in which a thermoplastic resin layer (A) is laminated on the side and a thermoplastic resin layer (B) is laminated on the other side, and the metal foil and the thermoplastic resin layer are laminated by extrusion lamination, and a thermoplastic resin layer is used ( The tensile strength of A) is Sa, the elongation at break is Ea, the tensile strength of thermoplastic resin layer (b) is Sb, and the elongation at break is Eb, the thermoplastic resin layer (A) And the thermoplastic resin layer (B) has a tensile strength ratio of

Sa/Sb=l/2 至 1/2〇,伸長度之比為 Ea/Eb = 1/0 8 至 1/〇 〇1 之關係,於熱塑性樹脂層(A)及熱塑性樹脂層(B)的至少 一方’在與金屬箔相反側的表面上積層熱封材層,將此 作為二次電池容器用積層材使用。 [先前技術文獻] [專利文獻] [專利文獻1]特開2003-288865號公報 [專利文獻2]特開2003-288866號公報 [專利文獻3]特開平7_76375號公報 201222930 【發明内容】 [發明所欲解決的問題] '而於電動汽車、混合動力汽車、電動 > 輪車中 使用此等的二次電池容器用積層材時,由於道路行缺中 勺振動有在外裝積層材中產生龜裂,或由於内部電池 的振動自外裝積層材内部側產生龜裂,亦傳遠至外部 」外裝積層材會破裂,發生電解液的洩漏,或電解液飛 月欠之虞又飞車等由於衝撞時的衝擊,其内的發電要 素破壞外裝材,有飛出到外面之虞。 本發明之課題在於提供一種即使經由道路行駛中的 動也不^在外層積層材產生龜裂,不會破裂,沒有 :::解液的洩漏、飛散之虞的二次電池容器用積層材 /、谷器再者’所使用的|呂箔係儘可能地薄,而減低廢 棄寺的裒i兄負荷。還有,提供—種即使在汽車等由於衡 撞時等的衝擊,外層積層材也不破壞設有用於封入發 電要素的深拉型部之大型容器用的二次電池容器用積層 材與大型容器。 [解決問題的手段] 本發明者們為了解決前述問題,專心致力地檢討,結 f發現藉由-種積層材,其係依順序積層有由聚對苯二甲 酉夂乙一酯、聚萘二甲酸乙二酯、 _ _ ^ ♦礼®文或對位糸芳香族聚 醯月女所成的薄膜(A) '尼龍6薄膜f只、上… . ^ a 潯膜(β)、鋁箔(C)、聚丙烯薄 膜(D)之積層材’其特徵為:a俜-紅Sa/Sb=l/2 to 1/2〇, the ratio of elongation is Ea/Eb = 1/0 8 to 1/〇〇1 in the thermoplastic resin layer (A) and the thermoplastic resin layer (B) At least one of the layers is laminated on the surface opposite to the metal foil, and this is used as a laminate for a secondary battery container. [PRIOR ART DOCUMENT] [Patent Document 1] JP-A-2003-288866 [Patent Document 3] JP-A-2003-288866 [Patent Document 3] JP-A-7-76375 The problem to be solved] When using the laminated material for secondary battery containers in electric vehicles, hybrid vehicles, electric vehicles, and the like, the turtles in the outer laminated materials are generated due to the vibration of the road in the road. Cracking, or cracking from the inside of the exterior laminated material due to the vibration of the internal battery, and it is transmitted to the outside." The outer laminated material may be broken, and electrolyte leakage may occur, or the electrolyte may not fly. Due to the impact at the time of collision, the power generation elements in the inside destroy the exterior material and fly out to the outside. An object of the present invention is to provide a laminate for a secondary battery container in which a crack occurs in an outer layered material and does not break even when moving through a road. The use of the glutinous rice is also as thin as possible, and the burden of the abandoned temple is reduced. In addition, it is possible to provide a laminate for a secondary battery container and a large container for a large-sized container provided with a deep-drawn portion for enclosing a power-generating element, even when an automobile or the like is impacted by a balance. . [Means for Solving the Problems] In order to solve the above problems, the inventors of the present invention have devoted themselves to reviewing, and it has been found that a layered material is laminated with poly(p-xylylene carbonate) and poly(naphthalene). Ethylene formate, _ _ ^ ♦ 礼® or a film made of para-aromatic polyfluorene (A) 'Nylon 6 film f only, upper... . ^ a enamel film (β), aluminum foil (C ), a laminate of polypropylene film (D) characterized by: a俜-red

片益χ上一 軸配向薄膜,Β及D 係無配向溥膜,在C與D之間有The film has a matching film on the upper axis, and the D-line has no alignment film. There is a gap between C and D.

,θ 令文吐聚烯烴層,而且D 的杨氏模數為500MPa以下,可作Λ β 2 a ^ ^ J作成耐振動性比以往還優 之一 < 電池用積層材,終於完成本發明。 201222930 烯烴係 基之接 又’在C與D之間的改性聚燁烴層之改性聚 接枝改性聚丙稀,較佳為經由接枝反應導入官能 枝改性聚丙稀。 另外,由聚對苯二甲酸乙二酯、聚萘二曱酸乙-酽 或聚乳酸所成的薄膜(A)之斷裂強度較佳炎 馬 1 5 0〜 250MPa,斷裂伸長度為1〇〇〜150%,可作成 J 辰動性比 以往還優異之二次電池用積層材。 還有,由聚對苯二甲酸乙二酯、聚萘二甲 曰夂6二酉旨 斷裂強度若為 Λ2 則可作成比以 再者由於可減 或對位系芳香族聚醯胺所成的薄膜(A)之 250〜480MPa’斷裂伸長度為80〜170%, 往還耐振動性優異之二次電池用積層材, 薄所使用的紹兔之厚度而較佳。 又,由聚 度若為100〜 成耐振動性、 積層材而較佳 對苯二甲酸乙二酯所成的薄膜(A)之街裂 25 0MPa ’斷裂伸長度為170%以上 則可作 耐衝擊性比以往還優異之大型二 —人%池用 積層材 再者’本發明係藉由上述記載的二次電池用 所形成之一次電池容器。 [發明的效果] 依Μ本發明,本發明的 it: 务 σ丨小〜依勒性 異’即使搭載於電動汽車、混合動力汽車、電氣自 輪車等,也沒有以下之虞:經由道路行駛中的振動,一 在外襞積層材產生龜裂、破裂’ #生内部電解液市 ,或電解液飛散。 ^ ϋ 201222930 又,若由聚對笨二甲酸乙二酯、聚萘二曱酸乙二酯 或對位系芳香族聚醯胺所成的薄膜(A)之斷裂強度為2 5 〇 〜480MPa,斷裂伸長度為8〇〜17〇%,且可更減薄所使 用的銘箔之厚度。 另外’若由聚對苯二曱酸乙二酯所成的薄膜(A)之斷 裂強度為100〜250MPa,斷裂伸長度為170%以上,則可 作成比以往還耐振動性、耐衝擊性優異之大型二次電池 用積層材’衝撞時的衝擊不會使外裝積層材破裂,或使 内部發電要素飛出。可適用於設有用於封入發電要素之 深拉成型部的大型容器。 【實施方式】 [實施發明的形態] 以下,詳細說明本發明。 _ 於本發明中,由聚對笨二曱酸乙二酯、聚萘二曱酸 乙二酯、聚乳酸或對位系芳香族聚醯胺所成的薄膜(A)( 以下亦僅稱A) ’就是以對笨二曱酸與乙二醇為主成分的 經由酯鍵所聚合的聚對苯二甲酸乙二酯藉由延伸而分子 配向之薄膜,以2,6-萘二羧酸與乙二醇為主成分的經由 酯鍵所聚合的聚萘二曱酸乙二酯藉由延伸而分子配向之 薄膜,乳酸經由酷鍵所聚合的聚乳酸藉由二軸延伸而分 子配向之4膜’或對苯二甲酸衍生物與對苯二胺衍生物 經由醯胺基所鍵結的芳香族聚醯胺藉由溶液製膜而成為 薄膜者,可使用眾所周知者。 作為芳香族聚醯胺,使用對苯二胺與對苯二曱醯氣 經由溶液聚合而得之聚對苯二甲醯對苯二胺,相當於9〇 201222930 莫耳%的2-氯對苯二胺' 相當於10莫耳%的4,4’-二胺基 二苯基醚、相當於100莫耳%的2 -氯對苯二曱醯氣經由 溶液聚合而得之聚2-氣對伸苯基4,4’-二胺基二苯基醚 2 -氣對苯二曱醯胺,聚苯甲醯胺,聚間伸苯基間苯二甲 醯胺等。芳香環上的氫原子之一部分亦可被鹵素(尤其氣 )、硝基、碳數1〜3的烧基(尤其甲基)、碳數1〜3的烧 氧基等之取代基所取代。構成聚合物的醯胺鍵中之氫亦 可被其它取代基所取代。具體地,於N-曱基吡咯啶酮( 以下稱為NMP)中,使作為芳香族二胺成分的相對於80 莫耳%的2-氣對苯二胺與相當於20莫耳%的4,4’-二胺基 二苯基喊溶解,於其中添加相當於 笨二曱醯氣’進行聚合,用氫氧化鋰來中和此,得到芳 香族聚酿胺溶液。使本聚合物溶液通過過濾器,然後通 過具有形成狹縫間隙的一對唇之喷嘴,在帶上流延,以 熱風加熱而使溶劑蒸發,將得到自己保持性的薄膜由帶 上連續地剝離,黏著於水/NMp比各自為ιη、2/ι、5/ι 的/辰度比之複數水槽内,依順序導入薄膜,進行 執,命;hj及無機鹽的萃取,用拉幅機進行水分 熱處理,而忐A — / ••‘、芩香族聚醯胺薄膜。於該期間,在薄膜 我度方向輿官择 280。。進行乾焊'向刀別進仃1.2倍、1.3倍延伸,在 芳香族聚酿々。處理後’徐徐冷卻等,而得到對位系 萘 ΐ it z t ’若不使用由聚對苯二曱酸乙二醋、聚 薄膜⑷,則保,、聚,酸或對位系芳香族聚醯胺所成的 L 、凌紹箔(C)的尼龍6薄膜f ώ私氺白 外部的振動時之士二由4σ & & 寻骐(Β)今易由於來自 力而磨彳貝破裂,此為不佳的。 201222930 從對電池用容器的成形性與電池用容器的耐振動性 並存之觀點來看,前述由聚對笨二甲酸乙二酯、聚萘二 甲酸乙二酯或聚乳酸所成的薄膜(A)之斷裂強度較佳為 150〜250MPa,斷裂伸長度較佳為1〇〇〜15〇%,斷裂強度 更佳為160〜240MPa,斷裂伸長度更佳為11〇〜13〇%。 若斷裂強度A 15〇MPa以上,則來自電池外側的振 動時之力係不易使外裝變形’不易產生龜裂,不易破裂 ’若斷裂強度A 25GMPa以下,則將電池用容器成形時 的加工特性(深拉性)良好,故斷裂強度更佳為^ 5〇〜 250MPa。 右;伸長度為1 00%以上,則將電池用容器成形時 的加工特性(深拉性)係良好,若斷裂伸長度為15〇%以下 1電池内的振動力係不易在外裝產生龜裂,不易破 裂,故斷裂伸長度更佳為100〜150%。 ,者’ A的厚度若比5_ #,則在電池容器成形時 工著時,外層不易破斷,若比3。_薄,則加 又’衣拉性)良好,故Α的厚度更佳為5〜3 0 μιη。 、以二為了儘可能地減薄電池用容器所使用的銘羯, =廢棄時的環境負荷,前述由聚對苯二甲酸乙二酿、 (Α)之斷VS:酷或對位系芳香族聚醯胺所成的薄膜 ,斷裂伸〜48°MPa,更…7°〜48〇MPa 範圍,〜:7°%,更佳為80〜13。%。若為此 易開孔而較佳Q二變形’:易破裂。即使被釘扎也不 全體的形離。 ,17使鋁箔(C)薄,也可保持電池容器 -10- 201222930 時之:斯:強編250MPa’由於來自電池外側的振動 —又 冑谷易變形’容易產生龜裂,容易破裂而不 ^電、、也^時’若^⑽厚度低於御m,則不易保 的形態而不宜。若斷裂強度高於48〇Mpa,或 性(深拉性;則將電池用容器成形時的加工特 …容= 若斷裂伸長度高於厲,則由 裔内部之電池振動時的力,外裝伸長 破裂而不宜。 |衣呷仗便夺易 再:’右八的厚度為4·5μιη以上,則在電池容器成 可二:解液附著時,外層不易破斷,即使受到振動也 二保…護機能,若比3〇_薄,則加工特性(深拉 )良好,故Α的厚度更佳為4.5〜3〇μηι。 為了製作对振動性、耐衝擊性比以往還優異之 =—次電池用積層材’前述由聚對苯二甲酸乙二酯所 的溥膜(Α)之斷裂強度為100〜250MPa,更佳為150〜 :晴Paj斷裂伸長度為17。%以上,更佳為190%以上。 右為此fe圍’則即使在製作設有深拉型部的大型容器時 對於外力不易變形’不易破裂。即使被釘扎也不易開 較佳為了 A車等因衝撞時的衝擊,其内的發電要 。不“破壞外裝材,不飛出到外自,也可增厚薄膜(八) 加工成為電池用容器。 若斷裂強度低於1 0〇MPa,則由於長時間的來自電池 1之振動日寸的力’外裝容易變形,容易產生龜裂,容 易破I。又,於汽車等的衝撞時,内部發電元件容易弄 破外裝材’飛出到外部而不宜。若斷裂強度高於250MPa -11 - 201222930 ,或斷裂伸長度低於m%,㈣^ 工特性(深拉性)降低而不宜。 益成形時的加 再者’ A的厚度愈厚, 而且汽車等衝撞時内部發不也::形狀愈穩定化’ ,作若A太旅。電件不θ私出到外部而較宜 .辛長度靶圍内,則即使80μιη :卜:,。若Α的厚度低於20Μηι左右,則在汽車 寻衝&時,内部發電元件容易飛出到外部而不宜。 本發明中’尼龍6薄膜(Β)(以下亦僅 由以頭法等斷眾所周知的尼龍6無配向= 的振:β: : Γ向:膜’則薄膜脆弱,由於來自電池外側 的振動時之力,外裝容易破裂而不宜。 尼龍6薄膜(Β)的厚;1Λ ρ ,Λ .川,予度右比1〇_厚,則Α容易破裂 右比30μιη溥’則加工特性 更佳為10〜30_。…生(冰拉性)良好,故Β的厚度 的銘箱(C)(以下亦㈣c)係可使用眾所周知 的心,其成分亦可使用眾所周知的純紹及銘合全。呈 體地,前述由聚對苯二甲酸乙二醋、聚萘二甲酸乙二酷 =乳酸所成的薄膜⑷之斷裂強度為15〇〜25〇 裂伸長度為⑽〜15G%時,C的厚度若為15_以上,則 在,易因容器内部的電池之振動,且容器外部的振 動時之力,發生變形或龜裂而較佳。 又’若前述由聚對苯二甲酸乙二醋、聚萘二甲酸乙 二醋或對位系芳香族聚醯胺所成的薄膜(A)之斷裂強度 為25 0〜480MPa,斷裂伸η*α〇λ 又 辦泉狎長度為80〜170%,則即使鋁 (C)的厚度減薄到10μιη為止,在銘箱也不易因容器内部 -12- 紹 、 (JIS)3003 、 3004 周 知 者 ,較佳 為 含 有 出 的 至 少一個 成 分 〇 箔 的 關 係上, 為 2. 0 上 的 、鐵或 矽 ? 有 防 止 針 孔或裂 紋 0 又 光 材 > 彼等的 中 間 材 適 宜 選 擇,從 成 形 性 材 0 又 ,按照 需 要 或 有 機 溶劑等 施 予 洗 於 本發明 中 5 聚 用 無 配 向薄膜 且 楊 氏 聚 丙 烯 薄膜。 201222930 的電池之振動,且容器外部的振動時之力, 或龜裂,可保持電池容器形態,故厚度更佳 上0 另外’若前述由聚對苯二曱酸乙二酯所) 之斷裂強度為1〇〇〜25〇Mpa«斷裂伸長度為 ,鋁箔(c)的厚度為10μπι以上時,則在鋁箔 内部的電池之振動,且容器外部的振動時之 變形或龜裂,可保持電池容器形態,故厚度」 以上。 厚度的上限係沒有特定,從成本之點 8〇μιη以下。紹的純度係特別的限制可採用 、5052 、 8021 、 8079 等 1.0重量%以上的由I孟、 上限係沒有特別的限制 重量%左右。藉由含有 效於提高積層材的硬拓 ’關於調質,亦可採用 之任一種,可按照所要 、黏著性等之點來看, 較佳為預先藉由水、洗 淨等。 丙烯薄膜(D)(以下亦僅 模數為500MPa以下的 而發生變形 為ΙΟμηι以 改的薄膜(Α) 17 0 %以上時 不易因容器 力,而發生 佳為1 〇 μ m 來看較佳為 工業用的純 合金等眾所 鐵、石夕中選 ,但在製造 1. 〇重量%以 I性(剛性), 退火材、軋 求的特性來 較佳為退火 *劑、酸、鹼 稱D)係可使 丨眾所周知之 -13- 201222930 與配卢 經由熱封成 配向的情沉 又,D έ 以下。此係 側的振動時 易振動,而 (C) ’ D 與 C 關於D 用於將電池 易發生漏液 聚丙烯薄膜 10Ο μπι。 於本發 改性聚烯烴 此處所 具有官能基 乙烯 '聚丙 來酸酐基、 結合性的官 丙稀酸、醋 酯等之共聚 特別地,官 即,於構成 合不飽和叛 二:相比,無配向薄膜係熱封溫度低,容易 ,二人電池用谷器而較佳。此係因為在無 ㈣L密封時聚丙稀分子的纏結係容易進展。 因拉數宜4 5GGMPa以下,更佳為45〇胁 .、’、揚氏模數若高於5〇〇MPa,則來自電池外 ^谷易傳達至容器内部的電池,電池容 ,谷窃内部的電池振動之力容易傳達至鋁箔 C與B容易剝離而不宜。 的薄膜厚纟’若厚度為25㈣以上,則提高 的:态成形之密封強度,密封不易脫落,不 1若厚度為10〇μΓη以下,則該厚度的無配向 係可在市場上容易取得,故厚度更佳為25〜 明中,在鋁箱(C)與聚丙烯薄膜(D)之間設置 層。 謂的改性聚烯烴(以下亦簡稱改性P〇),就是 成分的聚烯烴,作為改性聚烯烴,使用在聚 烯等的聚烯烴中導入胺基、羧基、羥基、馬 石夕烧基、丙烯酸基、丙烯酸酯基等之與紹有 能基者,將主單體的乙烯、丙烯等之烯烴與 酸乙烯@旨、甲基丙豨酸環氧丙酯、丙烤酸甲 單體聚合而得之烯烴共聚物等眾所周知者。 能基經接枝結合的接枝改性聚丙烯係較佳。 主骨架的聚丙稀之全部或一部分,接枝共聚 酸或其酐而成之接枝共聚物。構成改性聚丙 -14- 201222930 浠之主骨架的聚内嫌 單體所成的嵌段二係丙晞的均聚物’或丙稀與其它 例如可舉出乙/:或無規共聚物。作為其它單體’ 丁烯、3-曱基-丨—丁说丁烯、異丁烯、卜戊烯、2_甲基-1· 1 Λ掄、1鬼κ 締、^己烯、3-曱基-1-戊烯、2-甲基 -1-戊烯丨-庚烯等,此1 # ^ , ^ έΒ λ 此專係可於聚丙烯中含有1種或2 曰 内歸中的其它單體之含量通常為10重 置%以下。於此等之由 ’從成本方面來看,較佳為丙烯 均聚物、乙烯丙烯嵌段 , 又ν、1物、乙稀丙稀無規共聚物。 為了形成改性聚丙烯,从 ^ 作為對聚丙烯接枝共聚合的不飽 和缓酸或其肝(以下稱為「接枝單體」),例如可舉出丙 烯酉义f基丙稀等的不飽和單叛酸、馬來酸、富馬酸 伊康S欠榉康酸、烯丙基琥珀酸、中康酸、戊烯二酸 、納狄克(nadic)酸、甲基納狄克酸、四氫苯二曱酸、曱 基四氫苯二曱酸等的不飽和二羧酸、馬來酸酐、伊康酸 酐、檸康酸酐、烯丙基琥珀酸酐、戊烯二酸酐、納狄克 酸酐、曱基納狄克酸酐、四氫苯二甲酸酐、甲基四氫苯 =甲酸酐等的不飽和二羧酸酐等。改性聚丙烯亦可含有 單獨1種或2種以上的組合之此等接枝單體。於此等之 中,從成本面及物性面來看,較佳為馬來酸、馬來酸酐 、納狄克酸、納狄克酸酐。此改性聚丙烯中的接枝單體 之含量,從得到與鋁辖的黏著性及與聚丙烯薄膜的黏著 性優異之黏著劑組成物之點來看,為〇1〜1〇重量%,較 佳為0.5〜5重量%。 改性聚烯烴係容易與鋁箔(c)和聚丙烯薄膜這兩 者結合’藉由改性聚烯烴層’而減低汽車等之行駛時的 振動所致的D與C之剝離容易度。 -15- 201222930 改性聚烯烴層若厚度為 剝離’若厚度為50μηι以下 層破裂’故改性聚烯烴層的 改性聚烯烴層係可使用 塗覆•積層法而設置在C與 性聚烯烴所成的薄膜,可藉 與D的熱積層法來設置。 本發明的二次電池容器 之順序積層。D由於在以積 際,具有將D與D疊合而使 層。鋁箔 C,為了儘可能地 、衝擊力,且為了不被外部 成為最外層之内側,積層在 外部的力,在C上設置Β, 耗,必須將Α設置在最外層 若在最外層不使用A, 則B與外部摩擦而磨損, A/C/D/B等在離最外層的第 不被鋁箔吸收而傳達’ C容 裂。若在最外層積層C,則 變形、磨損、破壞而不宜。 本發明的積層材之製造 藉由以下的方法來形成。 可藉由乾積層法來黏著 萘二曱酸乙二酯、聚乳酸或 1〇μΐη以上,則c與D不易 ,則振動不易使改性聚烯烴 厚度更佳為1〇μιη至5〇μτη。 改丨生t烯煙樹脂,藉由壓出 D之間。又,亦可使用由改 由疊合C、改性聚烯烴薄膜 用積層材必須依照A/B/C/D 層材作為電池用容器成形之 密封之機能,故必須為最内 不受到來自袋外部的振動力 的氧所氧化,必須儘可能地 D上。為了保護C防止來自 為了不使B與外部摩擦而磨 〇 而成為 B/A/C/D、B/C/A/D, 電池用容器容易破裂。若為 2個積層C,則外部的振動 易龜裂,電池用容器容易破 由於來自外部之力,C容易 方法係沒有特別的限定’可 由聚對苯二曱酸乙二酯、聚 對位系芳香族聚醯胺所成的 -16 * 201222930 薄膜(A)、尼龍6薄膜(B)與鋁箔(〇。作為黏著劑,可使 用多元醇系主劑與異氰酸酯系硬化劑之通常二液型者。 ,體地,可舉出三井化學聚胺甲酸酯(股)製的 多凡醇系主劑)/Takenate(異氰酸酯系硬化劑)二液型。又 j亦可藉由壓出.塗覆積層法來黏著。作為壓出•塗覆 樹月曰使用各種聚乙婦、聚烯烴樹脂 '聚酿胺、聚醋、 —1、聚甲基戊烯、酸改性樹脂等。作為酸改性樹脂的 具體例’可使用三菱化學股份有限公司製的“—等。 作為聚酯樹脂,較佳為聚對苯二甲酸乙二酯。 ㈣紹f⑹與聚丙烯薄膜⑼’係可使用前述改性聚稀 :::融壓出的層當作。與D之間的夹層,進行層合而 膜疊合在…η改性聚烤烴所成的薄 層。與卜”加熱、加壓,藉由熱積層法來積 可將A與B黏著而成為a/r 。而成為A/B/C積層:广積層材,於此B#l黏著 娜⑽積層材。或者,可㈣D積層而得到 a 4+ , ^ . 、與6黏著而成為A/B積 層材,另外將C:與D積層 積 ., A X積層材,佶A/R接 層材與C/D積層材以B與 使A/B積θ 文 文 聚烯烃 polyolefin layer, and the Young's modulus of D is 500 MPa or less, can be used as Λ β 2 a ^ ^ J to make vibration resistance better than the previous one < Battery laminate, finally completed the present invention . 201222930 olefin-based grafting The modified polygraft-modified polypropylene of the modified polyfluorene hydrocarbon layer between C and D is preferably introduced into a functional branch-modified polypropylene via a grafting reaction. In addition, the film (A) formed of polyethylene terephthalate, polyethylene naphthalate or polylactic acid has a high breaking strength of Yanma 1 500 to 250 MPa and an elongation at break of 1 〇〇. ~150%, it can be used as a laminate for secondary batteries that is superior to the past. Further, if the breaking strength of polyethylene terephthalate or polynaphthalene 6 is Λ2, the ratio can be made to be smaller than that of the para-type aromatic polyamine. The film (A) has an elongation at break of from 250 to 480 MPa of 80 to 170%, and is preferably a laminate for a secondary battery which is excellent in vibration resistance and a thickness of a rabbit which is used for thinness. Further, if the degree of aggregation is 100 to the vibration resistance and the laminated material, the film (A) formed by the ethylene terephthalate is preferably 25 MPa, and the elongation at break is 170% or more. A large-sized two-person pool composite material which is superior in impact to the prior art. The present invention is a primary battery container formed by the above-described secondary battery. [Effects of the Invention] According to the present invention, the present invention is not limited to the following: even if it is mounted on an electric car, a hybrid car, or an electric self-wheeled vehicle, it is not the following: The vibration in the middle, the cracking and cracking of the slab in the outer layer is produced. ^ ϋ 201222930 In addition, if the film (A) formed by poly(p-butylene dicarboxylate), polyethylene naphthalate or para-type aromatic polyamine has a breaking strength of 25 〇 to 480 MPa, The elongation at break is 8〇~17〇%, and the thickness of the used foil can be further reduced. In addition, when the film (A) made of polyethylene terephthalate has a breaking strength of 100 to 250 MPa and an elongation at break of 170% or more, it is excellent in vibration resistance and impact resistance. In the case of a large-sized secondary battery laminate, the impact at the time of impact does not cause the outer laminate to be broken, or the internal power generation element to fly out. It is applicable to a large container provided with a deep drawing portion for enclosing a power generating element. [Embodiment] [Embodiment of the Invention] Hereinafter, the present invention will be described in detail. _ In the present invention, a film (A) (hereinafter also referred to as A) formed of polyethylene terephthalate, polyethylene naphthalate, polylactic acid or para-aramid. ' is a film of molecularly oriented polyethylene terephthalate polymerized by ester bond with stearic acid and ethylene glycol as the main component, with 2,6-naphthalene dicarboxylic acid and A film of a polyethylene naphthalate polymerized by an ester bond as a main component of ethylene glycol, a film which is molecularly aligned by extension, a polylactic acid polymerized by a lactic acid via a cold bond, and a molecular alignment of 4 films by biaxial stretching 'When a terephthalic acid derivative and an aromatic polyamine which is bonded to a p-phenylenediamine derivative via a guanamine group are formed into a film by a solution, a known one can be used. As an aromatic polyamine, poly(p-xylylene terephthalamide) obtained by solution polymerization of p-phenylenediamine and p-benzoquinone gas, equivalent to 9〇201222930 mol% of 2-chloro-p-benzene Diamine 'equivalent to 10 mol% of 4,4'-diaminodiphenyl ether, equivalent to 100 mol% of 2-chloroterephthalene gas obtained by solution polymerization of poly-2- gas pair Phenyl 4,4'-diaminodiphenyl ether 2- gas terephthalamide, polybenzamide, poly(phenylene phthalamide), and the like. A part of the hydrogen atom on the aromatic ring may be substituted with a substituent such as a halogen (especially gas), a nitro group, a carbon group having 1 to 3 carbon atoms (especially methyl group), and an alkoxy group having 1 to 3 carbon atoms. The hydrogen in the guanamine bond constituting the polymer may also be substituted by other substituents. Specifically, in the N-decylpyrrolidone (hereinafter referred to as NMP), the 2-di-p-phenylenediamine as an aromatic diamine component relative to 80 mol% and the equivalent of 20 mol% are 4 4'-Diaminodiphenyl group was dissolved, and a polymerization equivalent to stupid dioxane was added thereto, and this was neutralized with lithium hydroxide to obtain an aromatic polyamine solution. The polymer solution is passed through a filter, and then passed through a nozzle having a pair of lips forming a slit gap, cast on a belt, heated by hot air to evaporate the solvent, and the film which is self-retaining is continuously peeled off from the belt. Adhered to the water/NMp in a plurality of water tanks of different ratios of ιη, 2/ι, 5/ι/, and sequentially introduced into the film, and carried out the process of extracting, hj and inorganic salts, and using a tenter to carry out moisture. Heat treatment, while 忐A — / ••', eucalyptus polyamide film. During this period, I chose 280 in the direction of the film. . Dry-welding is carried out in a 1.2-fold, 1.3-fold extension to the knife. After treatment, 'slow cooling, etc., to obtain para-naphthoquinone it zt 'If not using polyethylene terephthalate, poly film (4), then, poly, acid or para-aromatic polyfluorene The L made of amine and the nylon 6 film of 凌绍箔 (C) f ώ ώ 外部 外部 外部 外部 由 由 由 由 由 由 由 由 由 由 由 由 由 由 由 由 由 由 由 由 由 由 由 , , , , , , , , , , , , , , , , , This is not good. 201222930 From the viewpoint of coexistence of moldability of a battery container and vibration resistance of a battery container, the film formed of polyethylene terephthalate, polyethylene naphthalate or polylactic acid (A) The breaking strength is preferably 150 to 250 MPa, the elongation at break is preferably from 1 to 15%, the breaking strength is more preferably from 160 to 240 MPa, and the elongation at break is more preferably from 11 to 13%. When the breaking strength A is 15 MPa or more, the force at the time of vibration from the outside of the battery is less likely to be deformed by the outer casing, and it is less likely to be cracked and is not easily broken. If the breaking strength is 25 or less, the processing characteristics when forming the battery container are obtained. (Deep drawing property) is good, so the breaking strength is better as ^ 5 〇 ~ 250 MPa. When the elongation is 100% or more, the processing characteristics (deep drawing property) when forming the battery container are good, and if the elongation at break is 15% or less, the vibration force in the battery is less likely to cause cracking in the exterior. It is not easy to be broken, so the elongation at break is preferably 100 to 150%. If the thickness of the 'A is greater than 5_#, the outer layer is not easily broken when the battery container is being formed. _Thin, then add and 'clothing' is good, so the thickness of the crucible is more preferably 5~3 0 μιη. In order to reduce the thickness of the battery container as much as possible, the environmental load at the time of disposal, the above-mentioned polyethylene terephthalate brewing, (Α) breaking VS: cool or para-aromatic The film formed by polyamine has a tensile elongation of ~48 ° MPa, more ... 7 ° ~ 48 〇 MPa range, ~: 7 °%, more preferably 80 to 13. %. If it is easy to open the hole, it is better to have a Q-deformation': it is easy to break. Even if it is pinned, it is not all. , 17 makes the aluminum foil (C) thin, can also keep the battery container -10- 201222930 when: S: strong woven 250MPa 'because of the vibration from the outside of the battery - and the valley is easy to deform 'easy to crack, easy to break without ^ If the thickness of the ^(10) is lower than the m, it is not easy to maintain. If the breaking strength is higher than 48 〇Mpa, or sex (deep drawing property; the processing when forming the battery container is special... If the elongation at break is higher than the violent, the force of the battery inside the internal vibration of the genus, the exterior It is not suitable for elongation and rupture. The 呷仗 呷仗 夺 易 易 易 易 易 易 易 易 易 易 易 易 易 易 易 易 易 易 易 易 易 易 易 易 易 易 易 易 易 易 易 易 易 易 易 易 易 易 易 易 易 易 易 易If the protective function is thinner than 3〇_, the processing characteristics (deep pull) are good, so the thickness of the crucible is preferably 4.5~3〇μηι. In order to produce a sub-battery that is superior to vibration and impact resistance. With the laminate material, the rupture strength of the ruthenium film (polyethylene terephthalate) of the foregoing polyethylene terephthalate is 100 to 250 MPa, more preferably 150 to 95: the elongation at break of the Paj is 17.5% or more, more preferably 190. % or more. If the right side is made of a large container having a deep-drawn type, it is not easily deformed for external force. It is not easy to be broken even if it is pinned. The power generation within it is not to "destroy the exterior materials, not to fly out to the outside, but also to thicken The film (8) is processed into a battery container. If the breaking strength is less than 10 MPa, the force from the vibration of the battery 1 for a long time is easily deformed, and cracks are likely to occur, which easily breaks I. In the collision of automobiles, etc., the internal power generation components are likely to break the outer material's flying out to the outside. If the breaking strength is higher than 250MPa -11 - 201222930, or the elongation at break is less than m%, (4) Deep pullability) is not suitable. It is better to add the shape of the 'A', the thicker the thickness of A, and the internal vibration of the car when it collides:: The shape is more stable', as if A is a brigade. It is preferable to go out to the outside. Even if the thickness of the crucible is less than 20Μηι, the internal power generating element is likely to fly out to the outside when the car is rushed & In the present invention, the 'nylon 6 film (Β) (hereinafter, only the well-known nylon 6 without alignment = the vibration of the film: β: : Γ: film) is weak, due to vibration from the outside of the battery. Force, the exterior is easy to break and not suitable. Nylon 6 film ( Thickness; 1Λ ρ , Λ .川,予度右1〇_厚, then Α easily rupture right than 30μιη溥', the processing characteristics are better 10~30_....sheng (ice pull) is good, so Β The thickness of the box (C) (hereinafter also referred to as (4) c) can be used in the well-known heart, and the ingredients can also be used in the well-known pure and well-known. In the above, the above-mentioned polyethylene terephthalate, poly The film (4) of naphthalene dicarboxylate = lactic acid has a breaking strength of 15 〇 25 and 25 〇 when the elongation is (10) 〜 15 G%, and if the thickness of C is 15 _ or more, the battery is easily inside the container. The vibration is generated, and the force at the time of vibration outside the container is preferably deformed or cracked. 'If the above-mentioned film (A) made of polyethylene terephthalate, polyethylene naphthalate or para-type aromatic polyamine has a breaking strength of 25 0 to 480 MPa, the elongation at break η* 〇λλ The length of the spring is 80~170%, even if the thickness of the aluminum (C) is reduced to 10μιη, it is not easy to be in the box. -12- Shao, (JIS) 3003, 3004, Preferably, the relationship between at least one of the constituent bismuth foils is 2. 0, iron or ruthenium; prevention of pinholes or cracks 0 and light materials> Further, a non-aligned film and a Young's polypropylene film which are washed in the present invention are applied as needed or in an organic solvent or the like. The vibration of the battery of 201222930, and the force or crack of the vibration outside the container, can maintain the shape of the battery container, so the thickness is better on the other 0, if the above-mentioned breaking strength of polyethylene terephthalate) When the thickness of the aluminum foil (c) is 10 μm or more, the vibration of the battery inside the aluminum foil and the deformation or cracking of the vibration outside the container can maintain the battery container. Form, so the thickness is above. The upper limit of the thickness is not specified, and the point from the cost is 8 〇 μηη or less. The purity of the system is particularly limited. It can be used in the range of 1.0% or more of 5052, 8021, 8079, etc., and the upper limit is not particularly limited by weight. Any one of the hardening materials which are effective for improving the laminated material may be used, and it may preferably be water, washed or the like in advance in terms of desired properties, adhesion, and the like. The propylene film (D) (hereinafter, only when the modulus is 500 MPa or less and the film is deformed to ΙΟμηι to change the film (Α) 17% or more is less likely to be caused by the container force, and preferably 1 〇μm is preferable. For the industrial use of pure alloys, such as iron, Shi Xizhong, but in the production of 1. 〇% by weight I (rigid), annealed material, rolling characteristics are preferably annealed * agent, acid, alkali called D The system can make the well-known 13-201222930 and the distribution of the collateral through heat sealing, D έ below. The vibration on the side of the system is easy to vibrate, and (C) ’ D and C are used to make the battery susceptible to leakage of the polypropylene film 10 Ο μπι. In the present modified polyolefin, the copolymerization of the functionalized ethylene 'polypropionic acid anhydride group, the binding of the official acrylic acid, the acetate, and the like, in particular, the official, in the composition of the unsaturated two: compared to The alignment film has a low heat sealing temperature and is easy to use, and the two-person battery is preferably a grain device. This is because the entanglement of polypropylene molecules is easy to progress in the absence of (iv) L sealing. The number of pulls should be less than 4 5 GGMPa, more preferably 45 〇., ', and if the Young's modulus is higher than 5 〇〇 MPa, the battery from the outside of the battery is easily conveyed to the inside of the container, the battery capacity, the inside of the burglary The force of the battery vibration is easily conveyed to the aluminum foil C and B is easily peeled off. If the thickness is 25 (four) or more, the sealing strength of the formed state is improved, and the seal is not easily peeled off. If the thickness is 10 〇μΓη or less, the thickness of the non-alignment system can be easily obtained in the market, so More preferably, the thickness is 25 to 5, and a layer is provided between the aluminum case (C) and the polypropylene film (D). A modified polyolefin (hereinafter also referred to as a modified P〇) is a polyolefin of a component, and as a modified polyolefin, an amine group, a carboxyl group, a hydroxyl group, and a horse base are introduced into a polyolefin such as a polyolefin. For the acryl-based, acrylate-based, and the like, the olefin of ethylene, propylene, etc. of the main monomer is polymerized with the acid ethylene, the glycidyl methacrylate, and the acrylic acid monomer. The olefin copolymer obtained is well known. Graft-modified polypropylene which is capable of graft-bonding is preferred. All or part of the polypropylene of the main skeleton is a graft copolymer obtained by grafting a copolymerized acid or an anhydride thereof. The homopolymer ' or propylene of the block dipyridamole formed by the polyacrylic monomer constituting the modified polypropylene-14-201222930 main skeleton may be, for example, a B/: or a random copolymer. As other monomers 'butene, 3-mercapto-fluorene-butene, butene, isobutylene, pentene, 2-methyl-1·1 Λ抡, 1 κκ, hexene, 3-mercapto 1-pentene, 2-methyl-1-pentene-heptene, etc., 1 # ^ , ^ έΒ λ This specialty can contain 1 or 2 other monomers in polypropylene. The content is usually 10% or less. From the viewpoint of cost, propylene homopolymer, ethylene propylene block, ν, 1, and ethylene propylene random copolymer are preferred. In order to form the modified polypropylene, the unsaturated acid or the liver (hereinafter referred to as "graft monomer") which is graft-polymerized with polypropylene may, for example, be propylene-based or propyl-based propylene. Unsaturated monosinetic acid, maleic acid, fukic acid Ikon S sulphonic acid, allyl succinic acid, mesaconic acid, glutaconic acid, nadic acid, methyl nadic acid , unsaturated dicarboxylic acid such as tetrahydrophthalic acid or mercaptotetrahydrophthalic acid, maleic anhydride, itaconic anhydride, citraconic anhydride, allyl succinic anhydride, glutaconic anhydride, Nadick An unsaturated dicarboxylic anhydride such as an acid anhydride, a quinone dicetic acid anhydride, a tetrahydro phthalic anhydride, or a methyltetrahydro benzene = a formal anhydride. The modified polypropylene may also contain such graft monomers in a single or a combination of two or more. Among these, maleic acid, maleic anhydride, nadic acid, and nadic anhydride are preferred from the viewpoint of cost and physical properties. The content of the graft monomer in the modified polypropylene is 〇1 to 1% by weight from the viewpoint of obtaining an adhesive composition excellent in adhesion to aluminum and adhesion to a polypropylene film. It is preferably 0.5 to 5% by weight. The modified polyolefin is easily combined with the aluminum foil (c) and the polypropylene film to reduce the ease of peeling of D and C due to vibration during running of an automobile or the like by modifying the polyolefin layer. -15- 201222930 If the thickness of the modified polyolefin layer is peeling 'if the thickness is less than 50μηι, the modified polyolefin layer can be set in C and polyolefin by coating and lamination method. The resulting film can be provided by a thermal lamination method with D. The secondary battery containers of the present invention are sequentially laminated. Since D is in the accumulation, it has a layer in which D and D are superposed. In order to prevent the impact of the aluminum foil C as much as possible, and in order to prevent the outer side from being the outermost layer, the external force is accumulated on the C, and the crucible must be placed on the outermost layer. Then, B wears out with external friction, and A/C/D/B or the like is not absorbed by the aluminum foil from the outermost layer to convey 'C-cracking. If C is laminated on the outermost layer, deformation, wear, and damage are not suitable. The production of the laminate of the present invention is carried out by the following method. When the naphthalene diacetate, polylactic acid or 1 〇μΐη or more is adhered by the dry laminate method, c and D are not easy, and the vibration is less likely to make the thickness of the modified polyolefin more preferably from 1 μm to 5 μμηη. Change the t-ene olefin resin by pressing between D. Further, it is also possible to use a function of sealing which is formed by laminating C and a modified polyolefin film laminate material in accordance with the A/B/C/D layer material as a battery container, and therefore it is necessary to be the innermost from the bag. Oxygen oxidation of the external vibrational force must be as much as possible on D. In order to protect C from being worn in order to prevent B from rubbing against the outside, it becomes B/A/C/D, B/C/A/D, and the battery container is easily broken. If it is two laminated layers C, the external vibration is easily cracked, and the battery container is easily broken. Due to the force from the outside, the C method is not particularly limited. It can be made of polyethylene terephthalate or poly-para-type. 16* 201222930 film (A), nylon 6 film (B) and aluminum foil (anthracene.) As a binder, a usual two-component type of a polyol-based main component and an isocyanate-based hardener can be used. The body type includes a two-liquid type of a trioxane-based main agent/Takenate (isocyanate-based curing agent) manufactured by Mitsui Chemicals Polyurethane Co., Ltd. And j can also be adhered by pressing and coating. As the extrusion and coating, a variety of polyethylenes, polyolefin resins, polyamines, polyesters, 1, polymethylpentene, acid-modified resins, and the like are used. As a specific example of the acid-modified resin, "--, etc., manufactured by Mitsubishi Chemical Corporation can be used. As the polyester resin, polyethylene terephthalate is preferred. (4) The film (9) and the polypropylene film (9) can be used. The above modified poly-dilution::: melted layer is used as the interlayer between D and D, and the film is laminated on the thin layer formed by ... η modified poly-baked hydrocarbon. Pressurization, by means of thermal layering, can bond A and B to become a/r. It becomes the A/B/C laminate: a wide-layer laminate, where B#l adheres to Na (10) laminate. Alternatively, (4) D can be layered to obtain a 4+ , ^ . , and adhere to 6 to form A/B laminate, and C: and D are laminated. AX laminate, 佶A/R laminate and C/D Laminated material with B and A/B product

積層材。 σ而黏者,而製造A/B/C/E —次電池容器係可藉由 的積層材片,以聚@ — 本叙明的積層材切出兩》 盆=邊1二:溥膜(D)成為内側的方式重疊,》 八一邊熱封而熔黏,以作 、置且見 積層材’以使聚丙稀薄膜d。又,亦可切出-“ 將側面的二邊熱封而熔 為内側的方式彎折一端 熔黏,以作成袋子。 -17- 201222930 又 二次電池容器係可藉由從本發 ^的積層材切出 兩片的積層材片,以由聚對笨二甲酸乙 〜知、聚萘二甲 i乙二酯、聚乳酸或對位系芳香族聚醯 上、& , 峨所成的潯膜(A) 成為外側的方式,用模具將一片的積層材深拉成带,< 設有用於封入發電要素的深拉型部之成形材與另一片= 積層材豐合在聚丙烯(D)側,經由埶封而校 „ …T叫‘黏,以作成容 益0 [實施例] 以下,藉由實施例來詳述本發明,惟 比— W ^准本發明不受此 專貫把例所限定《再者,各特性值传葬 值你精由以下的方法來 測疋。 (1) 斷裂強度、斷裂伸長度、揚氏模數 使用拉伸試驗機(Tensilon),在+宝 ^仕卞子碩速率300mm/ /刀鐘、寬度l〇mm、試料長度50inrn下,料铁一 士 a 办 卜对於薄膜的長度 =向;寬度方向,在^、65%RH的環境下,依據 ^ 7 127(1999年),測定斷裂強度、”伸長度、楊氏 杈數值。評價係對長度方向、寬度 列& 又刀向各自的斷裂強度 、畊裂伸長度、揚氏模數,各測定5 4 D夂,求得平均值, 將長度方向與寬度方向的平均值再平均而進—。 (2) 薄膜厚度 # 使用電子測微計(ANRITSU股份右、 「p 1 牧物有限公司製商品名 K-3 12A型」),於針壓3〇g下測定 障ώ J ,寻胰厚度、鋁箔的 )干I 0 (3) C與D之間的改性聚烯烴層之厚度 -18- 201222930 將A/B/C/D積層材的小片(2mmx2mm)包埋在環氧樹 脂⑴FINETEC(股)製的商品名「Ep〇m_t」)中,使用切 片枝將各包埋树脂切割成5 〇 n m厚度藉由透射型光學 顯微鏡(NIKON儀器股份有限公司製“EcHpse以〇〇,,),以 500倍的倍率觀察而求得。 (4)成形性 以聚酯薄膜(A)成為外側的方式,藉由模具來深拉成 型本發明的積層材。成型的大小為30mmx50mm的尺寸( 模具的凹部形狀),以成形時的深拉深度為自3mm起每 !_地深拉成型’由積層材沒有破損的最大深拉深度來 進行評價。最大深拉深度為5mm以上者係實用範圍,低 於5mm者係實用範圍以外。 (5 )耐振動性-1 從本發明的積層材切出2片的2〇Cmxl5cm之積層材 片’以聚丙稀薄膜(D)成為内側的方式重疊冑其三邊孰 封而熔黏’以作成袋子,於苴中 ^ 中置入1〇〇g下述試驗液, 置入作為電池構成體媪也丨邮, 丹取體杈擬體的鋁板(3_厚度Laminates. σ 而 黏 , 制造 制造 制造 制造 制造 制造 制造 制造 制造 制造 制造 制造 制造 制造 制造 制造 制造 制造 制造 制造 制造 制造 制造 制造 制造 制造 制造 制造 制造 制造 制造 制造 制造 制造 制造 制造 制造 制造 制造 制造 制造 制造 制造 制造 制造 制造 制造 制造 制造 制造D) The inner side is overlapped, and the eight sides are heat-sealed and melted to make, and see, the laminated material 'to make the polypropylene film d. In addition, it is also possible to cut out - "The two sides of the side are heat-sealed and melted to the inside so that one end is bent and melted to make a bag. -17- 201222930 The secondary battery container can be laminated by the present invention. Two pieces of laminated material are cut out from the material to form a mixture of polyethylene terephthalate, polynaphthalene, polylactic acid or para-aramid, & The film (A) is formed on the outer side, and one piece of the laminated material is deeply drawn into a belt by a mold, < a formed material for a deep-drawn portion for enclosing the power generating element is placed and the other piece = laminated material is ablated in polypropylene (D) On the side, the „ ... ... T is called 'sticky' to make a profit 0. [Embodiment] Hereinafter, the present invention will be described in detail by way of examples, but the invention is not subject to this purpose. The example is limited. "Furthermore, the value of the burial value of each characteristic value is measured by the following method. (1) Tensile strength, elongation at break, and Young's modulus are measured using a tensile tester (Tensilon) at a rate of 300 mm / / knife ring, width l 〇 mm, sample length 50 inrn a The length of the film = direction; the width direction, in the environment of ^, 65% RH, according to ^ 7 127 (1999), the breaking strength, "elongation, Young's 杈 value. The direction, the width of the column & the knife to each of the breaking strength, the cleavage elongation, the Young's modulus, each measured 5 4 D 夂, the average value was obtained, and the average of the length direction and the width direction were averaged again - (2) Film thickness # Using an electronic micrometer (ANRITSU shares right, "P 1 Herb Co., Ltd., trade name K-3 12A"), the barrier J was measured at a needle pressure of 3 〇g, and the thickness of the pancreas was found. , Aluminum foil) Dry I 0 (3) Thickness of modified polyolefin layer between C and D -18- 201222930 A small piece of A/B/C/D laminate (2mm x 2mm) is embedded in epoxy resin (1) FINETEC ( In the product name "Ep〇m_t" manufactured by the company, the embedded resin is cut into a thickness of 5 〇 nm by using a sliced branch. A microscope ("EcHpse" manufactured by NIKON Instruments Co., Ltd.) was observed at a magnification of 500 times. (4) Formability was deep drawn by a mold in such a manner that the polyester film (A) was outside. The laminated material of the present invention is molded. The size of the molding is 30 mm x 50 mm (the shape of the concave portion of the mold), and the deep drawing depth at the time of forming is from 3 mm per deep. The deep drawing depth of the laminated material is not broken. For evaluation, the maximum deep drawing depth is 5 mm or more, and the practical range is less than 5 mm. (5) Vibration resistance-1 Two pieces of 2〇Cmxl5cm laminated material are cut out from the laminated material of the present invention. The sheet was superimposed on the inside of the polypropylene film (D), and the three sides were sealed and melted to form a bag, and 1 〇〇g of the following test solution was placed in the ^中^, and placed as a battery constituting body.媪 丨 丨, Dan take the body of the aluminum plate (3_ thickness

Xl5Cmxl〇Cm)後,將袋口熱封而密閉。 5式驗液係使用在碳酸# 7 _ 你厌馱伸乙s日/奴酸伸乙基甲酯=1/1( 重量比)中加有六氟化磷酸鋰鹽(濃度i乃⑴者。 使用本熱封樣品,固定於括私 β χ ^疋於振動式驗機(IDEX股份有 限公司製“BF-50UD”),在玄、、σ ^ 切韦 ’在至/皿、振幅0.75mm(縱向),以 :°= _,將此當作1個循環,進行 8小時後,目視觀察熱封樣品的破 由以下基準來評價。 狀心措 -19- 201222930 〇:沒有看到破裂、漏液的變化。 △:在袋子雖然沒有可目視的龜裂、破裂,但梢微看到 漏液。 X在鈇子明顯看到龜裂,由該處發生漏液。 xx :袋子破裂,液的大部分茂漏。 (6)耐振動性_ 2 從本發明的穑屏u +τ1山,, ^ 、曰材刀出2片的20cmxl5cm之積層材 攸1片的積層材’將封入10cmx5cm、深度5mm的 ’電要素用之深拉型部’以聚㈣膜(A)成為外側的方式 :使用長邊、短邊5cm、角2匪、口模肩ri 2_ 货模肩0.5mm的模具’施予加壓壓力71^_2之壓力 ’ :土成形深度5mm的容器狀,於該容器部中置入20g 驗液置入作為電池構成體模擬體的鋁板㈠厚 f jcmxScm)後’將另一方的非成形積層材以聚丙烯 溥膜(D)成為内側的方式重疊,冑四邊熱封、熔❿,而作 成容器。 忒驗液係使用在碳酸伸乙酯/碳酸伸乙基曱酯=丨/ i ( 重里比)中加有六氟化磷酸鋰鹽(濃度15N)者。 使用本熱封樣品,固定於振動試驗機(IDEX股份有 限A司製BF_5〇UD”),在室溫、振幅〇 (縱向),以 =心掃拖10Hz —55Hz—>i〇Hz,將此當作}個循環,進行 8卜時後,目視觀察熱封樣品的破裂、漏液之狀態,藉 由以下基準來評價’〇、〇〜△及△係實用範圍,X及 X X係實用範圍以外。 〇.沒有看到破裂、漏液的變化。 -20- 201222930 〇〜△.在容器雖然沒有漏液,但稍微看到龜裂。 △:在袋子雖然沒有可目視的龜裂、破裂,但稍微看到 漏液。 X·在袋子明顯看到龜裂,由談處發生漏液, X X .袋子破裂,液的大部分洩漏。 (7)耐振動性-3 從本發明的積層材切出2片的2〇cmxl5cm之積層材 片,從1片的積層材,將封入15cmxl〇cm、深度 的發電要素用之深拉型部,以聚酯薄膜(A)成為外側的方 式,使用長邊15cm、短邊i〇cm、角2mm、口模肩R1 2韻 、衝模肩0.5mm的模具,施予加壓壓力8kg/cm2之壓力 ,形成成形深度10mm的容器狀,於該容器部中置入12〇g 下述試驗液,置入作為電池構成體模擬體的鋁板(3mm厚 度xl2Cmx8cm)後,將另一方的非成形積層材,以聚丙烯 薄膜(D)成為内側的方式重疊1四邊熱封、熔黏,而作 成容器。 式驗液係使用在碳酸伸乙酯/碳酸伸乙基曱酯=1 Μ ( 重里比)中加有六氟化磷酸鋰鹽(濃度^」m〇1/L)者。 使用本熱封樣品,固定 U疋於振動試驗機(IDEX股份有 限公司製“BF-50UD”),在官,、田上 牧至/皿、振幅〇.75mm(縱向),以 60 秒掃描 10Hz —55Hz->irm c ,士 ☆ Hz ’將此當作1個循環,進行 8小牯後,目視觀察埶 ^ ^樣。0的破裂、漏液之狀態,藉 由以下基準來評價,〇'n〜 v v ^ ^ m 〇 Λ及△係實用範圍,X及 X X係貫用把圍以外。 〇:沒有看到破裂、漏液的變化。 -21 - 201222930 〇〜△:在容器雖然没有漏液,佴稍微看到龜裂。 △.在袋子雖然沒有可目視的龜裂、破裂,但稍微看到 漏液。 X :在袋子明顯看到龜裂,由該處發生漏液 X X ·袋子破裂’液的大部分洩漏。 (8)时衝擊性 將上述(7)所作成的試驗液.鋁板封入容器,以長邊 與短邊所形成的面成為下側,在大理石的試驗台上,自 5公尺的高度重複落下(相當於時速35km的衝撞)。 次重複落下後,目視觀察容器的破裂、漏液之 狀態’藉由以下基準來評價,〇、Q〜△及△係實用範 圍,X及XX係實用範圍以外。 〇:沒有看到破裂、漏液的變化。 〇△在谷器雖然沒有漏液,但稍微看到龜裂。 △:在容器稍微看到龜冑,稍微看到漏液。 X :在容器明顯看到龜裂,由該處發生漏液。 XX :容器破裂’液的大部分沒漏。 [實施例1] 藉由乾積層法,剩_ A ,。 ^ ,,對厗度12μ1Ώ、斷裂強度為240MPa 斷裂申長度為118%的二軸配向聚對苯二 膜⑷(東麗股份有限公司冑A—」 广厚 與厚度15μιη、斷商‘)Ρ60) 又強度為l〇3MPa、斷裂伸長 的無配向尼龍ό薄膜^ Λ 度為3 98 /0 号犋(Β)(東麗溥膜加工股份After Xl5Cmxl〇Cm), the bag mouth is heat sealed and sealed. The 5 type test system is used in the case of carbonic acid # 7 _ 驮 驮 驮 s / 奴 奴 奴 奴 / / / / / / / / / / / / / ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( Using this heat-sealed sample, it is fixed in a vibrating test machine ("BF-50UD" manufactured by IDEX Co., Ltd.), in the Xuan, σ ^chewei 'in / dish, amplitude 0.75mm ( In the longitudinal direction, as follows: ° = _, this was taken as one cycle, and after 8 hours, the damage of the heat-sealed sample was visually observed and evaluated by the following criteria. 状心措-19- 201222930 〇: No cracks or leaks were observed Change in liquid △: Although there is no visible crack or rupture in the bag, the tip slightly sees leakage. X is clearly visible in the scorpion, and leakage occurs from there. xx: The bag is broken, the liquid (6) Vibration resistance _ 2 From the 穑 screen u + τ1 mountain of the present invention, ^, and the coffin knives, 2 pieces of 20cm x 15cm laminated material 攸 1 piece of laminated material 'will be sealed 10cm x 5cm, depth 5mm 'deep-drawn part for electric elements' is a way to make the poly (tetra) film (A) outer: using a long side, a short side 5cm, an angle 2匪, a die shoulder ri 2_ a die shoulder 0.5mm 'Pressure pressure of pressurizing pressure 71^_2': a container shape having a soil forming depth of 5 mm, in which 20 g of the test liquid is placed in the container portion, and an aluminum plate (a) having a thickness of f jcm x Scm as a battery body simulation body is placed. One of the non-formed laminates was superposed such that the polypropylene film (D) was inside, and the crucible was heat-sealed and melted to form a container. The test solution was used in which lithium hexafluorophosphate (concentration: 15 N) was added to ethyl carbonate/ethyl carbonate-ethyl phthalate = 丨 / i (rear ratio). Use this heat seal sample and fix it on the vibration tester (IDEX Co., Ltd. BF_5〇UD), at room temperature, amplitude 〇 (longitudinal), and = 10Hz - 55Hz -> i〇Hz This was taken as a cycle, and after 8 b, the state of rupture and liquid leakage of the heat-sealed sample was visually observed, and the practical ranges of '〇, 〇~△ and △ were evaluated by the following criteria, and the practical range of X and XX systems was evaluated. 〇. No change in rupture or leakage. -20- 201222930 〇~△. Although there is no liquid leakage in the container, the crack is slightly seen. △: Although there is no visible crack or crack in the bag, However, the liquid leakage was slightly observed. X·The crack was clearly seen in the bag, and the liquid leakage occurred from the talk. XX. The bag broke and most of the liquid leaked. (7) Vibration resistance-3 Cut from the laminated material of the present invention Two sheets of laminated sheets of 2〇cmxl5cm are produced, and a deep-drawn part for a power-generating element of 15cm×l〇cm and depth is sealed from one laminated material, and the polyester film (A) is used as the outer side. Pressing 15cm, short side i〇cm, angle 2mm, die shoulder R1 2 rhyme, die shoulder 0.5mm, pressurizing A pressure of 8 kg/cm 2 was applied to form a container having a molding depth of 10 mm, and 12 μg of the following test liquid was placed in the container portion, and an aluminum plate (3 mm thickness x 12 cm×8 cm) as a battery body simulation body was placed, and the other side was placed. The non-formed laminated material is formed by heat-sealing and melt-bonding the polypropylene film (D) so as to be inside. The test liquid is used in ethyl carbonate/ethyl carbonate-ethyl ester = 1 Μ (Liu Libi) is added with lithium hexafluorophosphate (concentration ^"m〇1/L). Using this heat seal sample, fix the U疋 to the vibration tester ("BF-50UD" made by IDEX Co., Ltd.), and scan it at 10 Hz in 60 seconds for the officer, the field to the / dish, the amplitude 〇.75mm (longitudinal). 55Hz->irm c, 士 ☆ Hz 'This is taken as one cycle, and after 8 hours, the 埶^^ sample is visually observed. The state of rupture and liquid leakage of 0 is evaluated by the following criteria, 〇'n~ v v ^ ^ m 〇 Λ and △ are practical ranges, and X and X X are used outside the circle. 〇: No changes in rupture or leakage were observed. -21 - 201222930 〇~△: Although there is no liquid leakage in the container, 佴 slightly sees cracks. △. Although there was no visible crack or crack in the bag, a slight leak was observed. X: The crack is clearly seen in the bag, and leakage occurs from the place where X X · bag ruptures. (8) Time-impact property The test liquid prepared in the above (7) was sealed in a container, and the surface formed by the long side and the short side was set to the lower side, and the test piece on the marble was repeatedly dropped from the height of 5 meters. (equivalent to a collision of 35km per hour). After the repeated dropping, the state of the container was observed by rupture and liquid leakage was evaluated by the following criteria: 〇, Q △ △ and △ are practical ranges, and X and XX are outside the practical range. 〇: No changes in rupture or leakage were observed. 〇 △ Although there is no liquid leakage in the grain, the crack is slightly seen. △: The turtle was slightly seen in the container, and a slight leak was observed. X: Cracks are clearly seen in the container, and leakage occurs from there. XX: The container ruptured' most of the liquid did not leak. [Example 1] By the dry layer method, _ A was left. ^ ,, for a twist of 12μ1Ώ, a breaking strength of 240MPa, a fracture length of 118%, a biaxial alignment poly(p-phenylene film) (4) (Dongli Co., Ltd. 胄A-", thick and thick 15μιη, 断商') Ρ 60) An unaligned nylon ruthenium film with a strength of l〇3MPa and elongation at break ^ Λ degree of 3 98 /0 犋 (Β) (Dongli 溥 film processing shares

「Rayfan」(註冊商標)Ν〇 14〇 『a司I 酸醋股份有限公司製的“Takel…井化學聚胺甲 iU(夕凡醇系主劑 -22- 201222930 )/ Takenate A-3 (異氰酸酯系硬化劑)”二液型(1 〇〇重量 伤/10重量份)黏著劑,作成A/B積層材。此處,黏著劑 塗布里以固體成分計在A側為5 g / m2,於a / b貼合後, 進行40°C、72小時的熟化(aging)處理。 藉由乾積層法,疊合A/B積層材、厚度4〇μπ1的鋁"Rayfan" (registered trademark) Ν〇 14〇 "Takel... well chemical polyamine iU (Urban alcohol base agent-22- 201222930) / Takenate A-3 (isocyanate) A hardening agent)" two-liquid type (1 〇〇 weight injury / 10 parts by weight) adhesive, made of A / B laminated material. Here, the adhesive application was carried out at a temperature of 5 g / m 2 on the A side, and after a / b bonding, the aging treatment was carried out at 40 ° C for 72 hours. Laminated A/B laminated material, aluminum with a thickness of 4〇μπ1 by dry laminate method

Ά (C)(住輕|g羯股份有限公司製“ ν e s p a ’’ 8 〇 2 1)、β與C ’使用二井化學聚胺甲酸酯股份有限公司製的“Takelac A-910(多元醇系主劑),,/“Takenate A_3(異氰酸酯系硬化Ά (C) (“ e espa '' 8 〇 2 1), β and C 'Takelac A-910 (polyol) manufactured by Mitsui Chemicals Polyurethane Co., Ltd. Main agent),, / "Takenate A_3 (isocyanate hardening)

d ) —液型(1 〇 0重量份/1 0重量份)黏著劑,作成a / B / C 積層材。此處黏著劑塗布量係在B側以固體成分計為 6g/m ’於B/c貼合後,進行45°C、8〇小時的熟化處理 〇 於A/B/C積層材上’將厚度7〇μιη的斷裂強度為 35MPa、斷裂伸長度為655%、揚氏模數為415MPa的無 配向聚丙烯薄膜(D)(東洋紡績股份有限公司製 邛丫161^1„1-〇:丁?1146,,)在 14(rc 的熔融溫度以 ι〇μιη 的 厚度壓出,使用改性聚烯烴(三井化學股份有限公司製, Β能基接枝改性聚丙烯“Ad〇mer qE84〇”)於c與D之間 的夾層,進行積層,作成本發明的A/B/c/D積層材。特 性係顯示於表1中。 [實施例2] 除了於實施例1中,代替二軸配向聚對苯二甲酸乙 —S曰薄膜(A) ’使用厚度15|im、斷裂強度為i6〇Mpa、斷 裂伸長度為128%的二軸配向聚乳酸薄膜(UNmKA股份 有限公司製‘Terramac,,TF)以外,與實施例1同樣地,作 成A/B/C/D積層材。特性係顯示於表i中。 -23- 201222930 [實施例3] 除了於實施例1中,作為二軸配向聚對苯二曱酸乙 二醋薄膜(A) ’使用厚度25 μηι、斷裂強度為225MPa、斷 裂伸長度為1 50%的二軸配向聚對苯二曱酸乙二酯薄膜 (U NITIK A股份有限公司製“ e m b 1 e t ”)以外,與實施例1 同樣地’作成A/B/C/D積層材。特性係顯示於表1中。 [實施例4 ] 除了於實施例1中,作為二軸配向聚對苯二甲酸乙 二S旨薄膜(A),使用厚度38μηι、斷裂強度為216MPa、斷 裂伸長度為11 0%的二軸配向聚對苯二曱酸乙二酯薄膜( 東洋紡績股份有限公司製“Esterfilm E5 100”)以外,與實 施例1同樣地,作成A/B/C/D積層材。特性係顯示於表 1中。 [實施例5 ] 除了於實施例1中,代替二軸配向聚對苯二曱酸乙 二酯薄膜(A),使用厚度35μπι、斷裂強度為150MPa、斷 裂伸長度為120%的二軸配向聚乳酸薄膜(UNITIKA股份 有限公司製’’ T e r r a m a c T F ”)以外’與實施例1同樣地,作 成A/B/C/D積層材。特性係顯示於表1中。 [實施例6] 除了於實施例1中,作為二軸配向聚對苯二甲酸乙 二酯薄膜(A),使用厚度6.5μιη、斷裂強度為275MPa、 斷裂伸長度為1 1 8 %的二軸配向聚對苯二甲酸乙二酯薄 膜(東麗薄膜加工股份有限公司製「Lumirr〇r」(註冊商標 )P375)以外,與實施例1同樣地,作成A/B/C/D積層材 。特性係顯示於表1中。 -24- 201222930 [實施例7] 除了於實施例1中,作為二軸配向聚對苯二曱酸乙 =西旨薄膜(A)’使用厚度4·5μη1、斷裂強度為27iMpa、 斷裂伸長度為i 06%的二轴配向聚對苯二甲酸乙二酯薄 膜(東麗股份有限公司製rLumirr〇r」(註冊商標)Μ)以 外’與實施例i同樣地,作成A/B/c/D積層材下。特性係 顯示於表1中。 [實施例8 ] 除了於實施例1中,作為聚丙烯薄膜(D),使用厚产 40μιη、斷裂強度為33MPa、斷裂伸 又 ^ 1农1甲長度為570%、楊氏 模數3 8 0 Μ P a的無配向聚丙稀薄膜(桌迷奸&土 守犋(果洋紡績股份有限公 司 1 “Pylenfilm-CT P1153”)以外,鱼每 , 興a %例1同樣地, 作成A/B/C/D積層材。特性係顯示於表i中。 [實施例9] 除了於實施例1中,作為聚丙稀薄膜⑼,使用厚度 Η)—斷裂強度為37MPa、斷裂伸長度為73〇%、楊: 模數為5GGMPa的無配向聚丙㈣膜(東洋紡績股份有限 公司製 “Pylenfilm-CT P 1 1 47”)以外,— ;Λ外’與實施例1同樣地 ,作成A/B/C/D積層材。特性係顯示於表i中。 [實施例10] 除了於實施例1中’作為聚丙烯薄膜⑼,使用厚戶 8〇μΙη、斷裂強度A 37MPa、斷裂伸長度為73()%、楊= 模數為50_的無配向聚丙烯薄膜(東洋纺績股份有限 公司製‘‘Pyunfum-CTP1147,,)以外,與實施例i同樣地 ,作成A/B/C/D積層材。特性係顯示於表i中。 -25- 201222930 [實施例11] 除了於實施例1中,作為聚丙烯薄膜(D),使用厚度 2 5μπι、斫裂強度為40MPa、斷裂伸長度為480%、楊氏 模數為500MPa的無配向聚丙烯薄膜(東洋紡績股份有限 公司製“Pylenfilm_CT P1181”)以外,與實施例i同樣^ ’作成A/B/C/D積層材。特性係顯示於表1中。 [實施例12] 除了於實施例1中,改性聚烯烴的夾層之厚度成為 30μηι以外,同樣地作成A/B/c/D積層材。特性係顯示於 表1中。 [實施例13] 除了於貫施例1中,作為改性聚烯煙,換成三井化 學股份有限公司製黏著性聚乙烯(官能基接枝改性聚乙 烯)“Adomer NE827”,夾層厚度為30μτη以外,同樣地作 成A/B/C/D積層材。特性係顯示於表1中。 [實施例14] 除了於實施例1中,作為改性聚烯烴,換成三井· 杜邦· POLYCHEMICAL股份有限公司製乙烯•醋酸乙 烯酯共聚物“Evaflex EV550”,夾層厚度為40μιη以外, 同樣地作成A/B/C/D積層材。特性係顯示於表1中。 [實施例1 5 ] 除了於實施例1中,作為改性聚烯烴,換成住友化 學股份有限公司製特殊乙烯系共聚物(乙烯/曱基丙烯酸 酯二曱基丙烯酸酯/丙烯酸曱酯=70/3/27wt%)“Bondfast 7L”,熔融溫度為1〇5°C以外,同樣地作成A/B/C/D積層 材。特性係顯示於表1中。 -26- 201222930 [實施例lq 土除^了於實施例1中’作為改性聚烯烴,換成東洋紡 1貝版伤有限公司製聚烯烴用熱熔性黏著劑“Toyotac M10〇 ,熔融溫度為160〇c以外,同樣地作成A/B/c/D積 層材°特性係顯示於表1中。 [實施例17彳 除了於實施例1中,作為改性聚烯烴,換成三菱化 子版伤有限公司製聚丙烯系黏著性樹脂(官能基接枝改 性聚丙烯“Modic P553A”),熔融溫度為168t: ’夾層厚度 為5〇μηΐ以外,同樣地作成A/B/C/D積層材。特性係顯 示於表1中。 [實施例1 8 ;| 除了於實施例1中’作為改性聚烯烴,使用三菱化 學股份有限公司製聚丙烯系黏著性樹脂(官能基接枝改 性聚丙烯“Modic Ρ553Α”)’熔融溫度為i68°c,夾層厚度 為60μηι以外,同樣地作成A/B/C/D積層材。特性係顯 示於表1中。 [實施例1 9 ] 除了於實施例1中,作為改性聚稀烴,使用三菱化 學股份有限公司製聚丙烯系黏著性樹脂(官能基接枝改 性聚丙稀“ModicP553A’’)’炼融溫度為i68°C,夾層厚度 為6μιη以外,同樣地作成A/B/C/D積層材。特性係顯示 於表1中。 [實施例20] -27- 201222930 除了於實施例1中,作為改性聚烯烴,使用三菱化 學股份有限公司製低搶度線狀聚乙稀糸黏著性樹脂(官 能基接枝改性聚乙烯“Modic M502”),熔融溫度為 以外,同樣地作成A/B/C/D積層材。特性係顯示於表1 中。 [實施例2 1 ] 除了於實施例1中,代替二轴配向聚對笨二曱酸乙 二酯薄膜(A),使用厚度12μηι、斷裂強度為3 1 OMPa、斷 裂伸長度為8 5 %的二轴配向聚萘二曱酸乙二酯薄膜(帝 人杜邦薄膜股份有限公司製“Teonex,’Q5l)以外,與實施 例1同樣地,作成A/B/C/D積層材。特性係顯示於表1 中。 [實施例2 2 ] 除了於實施例1中,作為二軸配向聚對苯二曱酸乙 二醋薄膜(A),使用厚度12μιη、斷裂強度為235MPa.、 斷裂伸長度為95%的二軸配向聚對苯二曱酸乙二酯薄膜 (東洋紡績股份有限公司製“Esterfilm” E5100)以外,與實 施例1同樣地,作成A/B/C/D積層材。特性係顯示於表 1中。 [實施例2 3 ] 除了於實施例1中,作為二轴配向聚對苯二曱酸乙 二酷薄膜(A),使用厚度16μιη、斷裂強度為285MPa、斷 裂伸長度為125%的二軸配向聚對苯二甲酸乙二酯薄膜( 帝人枉邦薄膜股份有限公司製“Teigin Tetoron Film” G2) 以外’與實施例1同樣地,作成A/B/C/D積層材。特性 係顯示於表1中。 28- 201222930 [實施例24] 於實施例1中,作為A,使用厚度12 K111的斷裂強 度為2 0 5 Μ P a、斷裂伸長度為9 5 %的二軸配向聚酯薄膜 (A)(東洋紡績股份有限公司製“Esterfilm E7700”)。其它 係與實施例1同樣地,作成A/B/C/D積層材。特性係顯 示於表1中。 [實施例25] 於實施例1中,在A/B/C積層材與d之間,疊合厚 度30μηι的改性聚丙稀薄膜(TOHCELLO股份有限公司製 “Adomerfilm QE-060C”),以棍溫度 15〇°C、幸昆壓力 30kg/cm、輸送速度20m/分鐘’藉由熱積層法來熱壓黏 ,作成A / B / C / D積層材。特性係顯示於表1中。 [實施例26] 除了於貫施例1中’C的厚度成為以外,與實 施例1同樣地’作成A/B/C/D積層材。特性係顯示於表 1中。 [實施例27] 除了於實施例1中,c的厚度成為8〇μηι以外,與實 她例1同樣地,作成A/B/C/D積層材。特性係顯示於表 1中。 [實施例28] 除了於實施例1中,作為二軸配向聚對苯二甲酸乙 二_薄膜⑷’使用厚度5〇μπι、斷裂強度為⑼购、斷 裂伸長度為3 6 5 %的二軸配向平剩_ — ^ ^ 门1對求二曱酸乙二酯薄膜( 帝人杜邦薄膜股份有限公司製 J衣i etlex FT7”)以外,與實 -29- 201222930 施例1同樣地’作成A/B/C/D積層材。特性係顯示於表 1中。 [實施例29] 除了於實施例1中,作為二軸配向聚對笨二甲酸乙 二酯薄膜(A),使用厚度14μηι、斷裂強度為7〇Mpa、斷 裂伸長度為88%的二軸配向聚對苯二曱酸乙二酷薄膜( 東洋紡績股份有限公司製“Tearfine TF1 10”)以外,與實 施例1同樣地,作成A/B/C/D積層材。特性係顯示於表 1中。 [實施例30] 藉由乾積層法,對厚度6·5μιη、斷裂強度為275MPa 、斷裂伸長度為1 1 8 %的二軸配向聚對苯二甲酸乙二酯薄 膜(A)(東麗股份有限公司製「Lumirr〇r」(註冊商標)p375) 與厚度15μπι、斷裂強度為1〇3MPa、斷裂伸長度為 的無配向尼龍6薄膜(B)(東麗薄膜加工股份有限公司製 「Rayfan」(註冊商標)NO 1401),使用三井化學聚胺甲 酸醋股份有限公司製的“Takelac A-910(多元醇系主劑 )’’/“Takenate Α·3(異氰酸酯系硬化劑),’二液型⑼重量 份/10重量份)黏著劑,作成Α/Β積層材《此處,黏著劑 塗布量以固體成分計在Α側為5g/m2,於Α/Β貼合後, 進仃40 C、72小時的熟化處理。 錯由乾積層法’疊合A/B積層材、厚度25μιη的鋁箔 (C)(住fe鋁箔股份有限公司製8〇2ι)、β與匸,使 用一井化學聚胺甲酸酯股份有限公司製的“Takelac 9 〇(多元醇系主劑),,/‘‘Takenate A-3 (異氰酸酯系硬化 -30- 201222930 劑)”二液型(100重量份/10重量份)黏著劑,作成a/b/c 積層材。此處黏著劑塗布量係在B側以固體成分計為 6g/m2 ’於B/C貼合後,進行45°C、80小時的熟化處理。 於A/B/C積層材上’將厚度70μηι的斷裂強度為 3 5MPa、斷裂伸長度為655%、楊氏模數為4i5MPa的無 配向聚丙烯薄膜(D)(東洋紡績股份有限公司製 “?丫161^11!1-(:丁?1146’’)在140°〇的熔融溫度,以1(^111的 厚度壓出,使用改性聚烯烴(三井化學股份有限公司製, 官能基接枝改性聚丙烯“Adomer QE84〇”)於C與D之間 的夾層’進行積層,作成本發明的A/B/C/D積層材。特 性係顯示於表1中。 [實施例3 1 ] 除了於實施例3 0中,作為二軸配向聚對苯二曱酸乙 二酯薄膜(A),使用厚度4.5 μηι、斷裂強度為271 MPa、 斷裂伸長度為 1 0 6 %的二軸配向聚對苯二甲酸乙二酯薄 膜(東麗股份有限公司製「Lumirror」(註冊商標)F53), 鋁箔(C)的厚度為30μιη以外,與實施例30同樣地,作成 A/B/C/D積層材。特性係顯示於表1中。 [實施例32] 除了於實施例3 0中,代替二軸配向聚對苯二甲酸乙 二酯薄膜(Α),使用厚度1 2μηι、斷裂強度為3 lOMPa、斷 裂伸長度為8 5 %的二軸配向聚萘二曱酸乙二酯薄膜(帝 人杜邦薄膜股份有限公司製“Teonex” Q5 1),鋁箔(C)的厚 度為1 Ομιη以外,與實施例30同樣地,作成A/B/C/D積 層材。特性係顯示於表1中。 -31- 201222930 [實施例3 3 ] 除了於實施例30中,作為二軸配向聚對苯二曱酸乙 二酯薄膜(A),使用厚度16 μιη、斷裂強度為285 MPa、斷 裂伸長度為125%的二軸配向聚對苯二曱酸乙二酯薄膜( 帝人杜邦薄膜股份有限公司製“ T e i g i η T e t 〇 r ο n F i 1 m ’’ G 2) ’銘箔(c)的厚度為1 > μηι以外,與實施例30同樣地,作 成A/B/C/D積層材。特性係顯示於表1中。 [實施例34] 除了於實施例30中,代替二軸配向聚對苯二甲酸乙 二醋薄膜(Α),使用厚度4.5μπι、斷裂強度為480MPa、 斷裂伸長度為8 0 %的對位系芳香族聚醯胺薄膜(東麗股 份有限公司製「Mictron」(註冊商標)Gq),鋁镇的厚 度為ΙΟμπι以外,與實施例30同樣地,作成a/B/C/D積 層材。特性係顯示於表1中。 [實施例35] 除了於實施例30中,作為聚丙烯薄膜(D),使用厚 度40μΐη、斷裂強度為33MPa、斷裂伸長度為57〇%、楊 氏模數3 80MPa的無配向聚丙烯薄膜(東洋紡績股份有限 公司製“Pylenmm-CTPUM,’)以外,與實施例3〇同樣地 ’作成A/B/C/D積層材。特性係顯示於表1中。 [實施例36] 除了於實施例30中,作為聚丙烯薄膜(D),使用厚 37MPa'”伸長度為 73〇%、楊 氏模數為50GMPa的無配向聚丙烯薄膜(東洋纺績股份有 限公司製“Pyienfnm-CTP1147,,)以外,與實施命"〇同樣 地,作成A/B/C/D積層材。特性係顯示於表!中。 -32- 201222930 [實施例37] 除了於實施例3 0中,作為聚丙烯薄膜(d ),使用厚 度80 μηι、斷裂強度為37 MPa、斷裂伸長度為730%、楊 氏模數為500MPa的無配向聚丙烯薄膜(東洋紡績股份有 限公司製“Pylenfilm-CT P1 147”)以外,與實施例30同樣 地,作成A/B/C/D積層材。特性係顯示於表1中。 [實施例38] 除了於實施例30中,作為聚丙烯薄膜(〇),使用厚 度25μπι、斷裂強度為40MPa、斷裂伸長度為480%、楊 氏模數為5 0 0 Μ P a的無配向聚丙歸薄膜(東洋紡績股份有 限公司製“ P y丨e n f i 1 m - C T P 1 1 8 1 ”)以外,與實施例3 0同樣 地,作成A/B/C/D積層材。特性係顯示於表1中。 [實施例39] 除了於實施例3 0中,改性聚烯烴的夾層之厚度成為 3 0μιη以外,同樣地作成A/B/C/D積層材。特性係顯示於 表1中。 [實施例4 0 ] 除了於實施例3 0中’作為改性聚烯烴,換成三井化 學股份有限公司製黏著性聚乙烯(官能基接枝改性聚乙 烯)“Adomer ΝΕ827”,夾層厚度為30μιη以外,同樣地作 成A/B/C/D積層材。特性係顯示於表1中。 [實施例4 1 ] 除了於實施例3 0中,作為改性聚烯烴,換成三井· 杜邦· POLYCHEMICAL股份有限公司製乙烯.醋酸乙 烯酯共聚物“Evaflex EV550” ’夾層厚度為4〇μιη以外, 同樣地作成A/B/C/D積層材。特性係顯示於表1中。 -33- 201222930d ) - Liquid type (1 〇 0 parts by weight / 10 parts by weight) of adhesive to form a / B / C laminate. Here, the amount of the adhesive applied is 6 g/m on the B side as a solid content, and after bonding at B/c, the curing treatment at 45 ° C for 8 hours is carried out on the A/B/C laminate. A non-aligned polypropylene film (D) having a thickness of 7 〇 μιη with a breaking strength of 35 MPa, an elongation at break of 655%, and a Young's modulus of 415 MPa (made by Toyobo Co., Ltd. 邛丫 161^1„1-〇: ?1146,,) is extruded at a thickness of 14 (the melting temperature of rc is ι〇μηη, using modified polyolefin (manufactured by Mitsui Chemicals, Inc., Β-based graft modified polypropylene "Ad〇mer qE84〇" The interlayer between c and D was laminated to form an A/B/c/D laminate of the invention. The characteristics are shown in Table 1. [Example 2] In addition to the second embodiment, instead of the two axes Oriented polyethylene terephthalate film (A) 'Using a thickness of 15|im, a breaking strength of i6〇Mpa, and an elongation at break of 128%, a biaxial alignment polylactic acid film (Terramac, manufactured by UNmKA Co., Ltd.) In the same manner as in Example 1, except that TF), an A/B/C/D laminate was produced. The characteristics are shown in Table i. -23- 201222930 [Example 3] In Example 1, as a biaxially oriented polyethylene terephthalate film (A) 'Using a thickness of 25 μηι, a breaking strength of 225 MPa, and an elongation at break of 150%, the biaxially aligned polyparaphenylene An A/B/C/D laminate was produced in the same manner as in Example 1 except that the ethylene phthalate film ("Emb1" manufactured by U NITIK A Co., Ltd.) was used. The characteristics are shown in Table 1. Example 4] In addition to Example 2, as a biaxially oriented polyethylene terephthalate film (A), a biaxial alignment pairing having a thickness of 38 μm, a breaking strength of 216 MPa, and an elongation at break of 110% was used. An A/B/C/D laminate was produced in the same manner as in Example 1 except that the ethylene phthalate film ("Esterfilm E5 100" manufactured by Toyobo Co., Ltd.) was used. The characteristics are shown in Table 1. Example 5] In addition to the biaxially oriented polyethylene terephthalate film (A), a biaxially oriented polylactic acid having a thickness of 35 μm, a breaking strength of 150 MPa, and an elongation at break of 120% was used in addition to Example 1. Thin film ("Terramac TF" made by UNITIKA Co., Ltd.) In the same manner as in Example 1, an A/B/C/D laminate was produced. The characteristics are shown in Table 1. [Example 6] In addition to Example 1, a biaxially oriented polyethylene terephthalate film was used ( A) A biaxially-oriented polyethylene terephthalate film having a thickness of 6.5 μm, a breaking strength of 275 MPa, and an elongation at break of 181% ("Lumirr〇r" manufactured by Toray Film Processing Co., Ltd. (registered) In the same manner as in Example 1, except for the trademark P375), an A/B/C/D laminate was produced. The characteristics are shown in Table 1. -24-201222930 [Example 7] Except that in Example 1, as the biaxially-oriented poly(p-terphenylene phthalate), the film (A)' had a thickness of 4·5 μη1, a breaking strength of 27 μMpa, and an elongation at break. i 06% of the biaxially-oriented polyethylene terephthalate film (rLumirr〇r (registered trademark) 东) manufactured by Toray Industries, Inc., in the same manner as in Example i, A/B/c/D Under the laminated timber. The characteristics are shown in Table 1. [Example 8] In addition to Example 1, as the polypropylene film (D), a thick product of 40 μm, a breaking strength of 33 MPa, a tensile elongation and a length of 570%, and a Young's modulus of 380 were used.无 P a non-aligned polypropylene film (Table 迷 && 土 犋 犋 ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( ( C/D laminate. The characteristics are shown in Table 1. [Example 9] Except for Example 1, as the polypropylene film (9), the thickness Η) was used, the breaking strength was 37 MPa, and the elongation at break was 73%. Yang: A non-aligned polypropylene (tetra) film having a modulus of 5 GG MPa ("Pylenfilm-CT P 1 1 47" manufactured by Toyobo Co., Ltd.), -; outside the same as in the first embodiment, A/B/C/ was prepared. D laminated material. The characteristics are shown in Table i. [Example 10] Except that in Example 1, 'as a polypropylene film (9), a non-orthogonal polyglybdenum 8 〇μΙη, a breaking strength A 37 MPa, an elongation at break of 73 ()%, and a yang = modulus of 50 Å were used. An A/B/C/D laminate was produced in the same manner as in Example i except that the propylene film ("Pyunfum-CTP1147" manufactured by Toyobo Co., Ltd.) was used. The characteristics are shown in Table i. -25-201222930 [Example 11] Except that in Example 1, as the polypropylene film (D), a thickness of 25 μm, a splitting strength of 40 MPa, an elongation at break of 480%, and a Young's modulus of 500 MPa were used. An A/B/C/D laminate was produced in the same manner as in Example i except for the alignment of a polypropylene film ("Pylenfilm_CT P1181" manufactured by Toyobo Co., Ltd.). The characteristics are shown in Table 1. [Example 12] An A/B/c/D laminate was produced in the same manner as in Example 1 except that the thickness of the interlayer of the modified polyolefin was 30 μm. The characteristics are shown in Table 1. [Example 13] In addition to the modified example 1, the modified polyene was replaced by an adhesive polyethylene (functional graft-modified polyethylene) "Adomer NE827" manufactured by Mitsui Chemicals Co., Ltd., and the interlayer thickness was A/B/C/D laminates were prepared in the same manner as in the case of 30 μτη. The characteristics are shown in Table 1. [Example 14] In the same manner as in Example 1, the modified polyolefin was replaced with an ethylene/vinyl acetate copolymer "Evaflex EV550" manufactured by Mitsui & Co., Ltd., and the thickness of the interlayer was 40 μm. A/B/C/D laminate. The characteristics are shown in Table 1. [Example 1 5] In addition to the modified polyolefin, it was replaced with a special vinyl copolymer (ethylene/mercaptoacrylate dimercapto acrylate/decyl acrylate) of Sumitomo Chemical Co., Ltd. in Example 1. /3/27 wt%) "Bondfast 7L", A/B/C/D laminate was produced in the same manner except that the melting temperature was 1 〇 5 °C. The characteristics are shown in Table 1. -26- 201222930 [Example lq soil removed in Example 1 as a modified polyolefin, replaced with Toyotec M10〇, a hot melt adhesive for polyolefins manufactured by Toyobo 1 Becker Co., Ltd., melting temperature is The characteristics of A/B/c/D laminates were similarly shown in Table 1 except for 160 〇c. [Example 17] In addition to the modified polyolefin in Example 1, it was changed to Mitsubishi Chemical Edition. Polypropylene adhesive resin (functionalized graft-modified polypropylene "Modic P553A") manufactured by Injury Co., Ltd., melting temperature: 168t: 'The thickness of the interlayer is 5〇μηΐ, and A/B/C/D layer is formed in the same manner. The properties are shown in Table 1. [Example 1 8 ; | In addition to the modified polyolefin in Example 1, a polypropylene-based adhesive resin manufactured by Mitsubishi Chemical Corporation was used (functional graft modification) Polypropylene "Modic Ρ 553 Α") 'The melting temperature was i68 ° C, and the interlayer thickness was 60 μηι, and the A/B/C/D laminate was similarly produced. The characteristics are shown in Table 1. [Example 1 9] In Example 1, as a modified poly-hydrocarbon, Mitsubishi Chemical Corporation was used. Polypropylene based adhesive resin (functional groups graft-modified polypropylene "ModicP553A '') 'refining melting temperature of i68 ° C, than the thickness of the interlayer 6μιη, creating the same manner as A / B / C / D laminate material. The characteristics are shown in Table 1. [Example 20] -27-201222930 In addition to Example 1, in the modified polyolefin, Mitsubishi Chemical Co., Ltd. was used to make a low-stretch linear polyethylene-adhesive adhesive resin (functional graft-modified polyethylene). "Modic M502"), except for the melting temperature, was similarly formed into an A/B/C/D laminate. The characteristics are shown in Table 1. [Example 2 1] In addition to the second embodiment, in place of the biaxially-aligned polyethylene terephthalate film (A), a thickness of 12 μm, a breaking strength of 31 MPa, and an elongation at break of 85 % were used. An A/B/C/D laminate was produced in the same manner as in Example 1 except that the polyethylene diethylene naphthalate film (Teonex, 'Q5l) manufactured by Teijin DuPont Film Co., Ltd. was used. [Table 2] [Example 2 2] In addition to Example 1, as a biaxially oriented polyethylene terephthalate film (A), a thickness of 12 μm, a breaking strength of 235 MPa, and an elongation at break of 95 were used. A/B/C/D laminate was produced in the same manner as in Example 1 except that a biaxially-oriented polyethylene terephthalate film (Esterfilm E5100, manufactured by Toyobo Co., Ltd.) was used. [Table 2] [Example 2 3] In addition to Example 1, as a biaxially oriented polyethylene terephthalate film (A), a thickness of 16 μm, a breaking strength of 285 MPa, and an elongation at break of 125 were used. % biaxially oriented polyethylene terephthalate film (made by Teijin Silicon Film Co., Ltd. In the same manner as in Example 1, except for Teigin Tetoron Film" G2), an A/B/C/D laminate was produced. The characteristics are shown in Table 1. 28-201222930 [Example 24] In Example 1, as A A two-axis alignment polyester film (A) having a breaking strength of 12 K111 and a breaking elongation of 95% (Esterfilm E7700, manufactured by Toyobo Co., Ltd.) was used. In the same manner as in Example 1, an A/B/C/D laminate was produced. The characteristics are shown in Table 1. [Example 25] In Example 1, a laminate was formed between the A/B/C laminate and d. A modified polypropylene film having a thickness of 30 μm ("Adomerfilm QE-060C" manufactured by TOHCELLO Co., Ltd.) is heated by a thermal lamination method at a stick temperature of 15 °C, a temperature of 30 kg/cm, and a transport speed of 20 m/min. The pressure-sensitive adhesive was used to form an A / B / C / D laminate. The characteristics are shown in Table 1. [Example 26] A was prepared in the same manner as in Example 1 except that the thickness of 'C was changed in Example 1 /B/C/D laminate. The characteristics are shown in Table 1. [Example 27] Except that in Example 1, the thickness of c was 8 〇μηι, In the same manner, an A/B/C/D laminate was produced. The characteristics are shown in Table 1. [Example 28] In addition to Example 1, the biaxially oriented polyethylene terephthalate film (4) was used. Using a thickness of 5 〇μπι, a breaking strength of (9), and an elongation at break of 3 6 5 %, the biaxial alignment is _ ^ ^ ^ Gate 1 to find a film of ethylene diacetate (made by Teijin DuPont Film Co., Ltd. In the same manner as in the first embodiment of the actual -29-201222930, an A/B/C/D laminated material was produced in the same manner as in the case of the clothing i etlex FT7"). The characteristics are shown in Table 1. [Example 29] In addition to Example 2, as a biaxially oriented polyethylene terephthalate film (A), a biaxial alignment having a thickness of 14 μm, a breaking strength of 7 〇Mpa, and an elongation at break of 88% was used. A/B/C/D laminate was produced in the same manner as in Example 1 except that a polyethylene terephthalate film (Tearfine TF1 10 manufactured by Toyobo Co., Ltd.) was used. The characteristics are shown in Table 1. [Example 30] A biaxially oriented polyethylene terephthalate film (A) having a thickness of 6·5 μm, a breaking strength of 275 MPa, and an elongation at break of 181 % by dry-laid method (Dongli Co., Ltd.) Co., Ltd. "Lumirr〇r" (registered trademark) p375) and an unaligned nylon 6 film (B) having a thickness of 15 μm, a breaking strength of 1 〇 3 MPa, and an elongation at break ("Rayfan" manufactured by Toray Film Processing Co., Ltd.) (registered trademark) NO 1401), "Takelac A-910 (polyol-based main agent)"' / "Takenate Α·3 (isocyanate-based curing agent), "two liquids" manufactured by Mitsui Chemicals Polyurethane Co., Ltd. Type (9) parts by weight/10 parts by weight) of adhesive to form Α/Β 层 《 《 此处 此处 《 《 《 《 《 《 《 《 《 《 《 《 《 《 《 《 《 此处 《 此处 《 《 此处 《 此处 C C C C C C C C C C C C C C C C , 72 hours of ripening treatment. Mistaken by dry-lamination method 'A/B laminated material, aluminum foil (C) with a thickness of 25μηη (8〇2ι made by Fe Aluminum Foil Co., Ltd.), β and 匸, using Yijing Chemical Polyurethane Co., Ltd. "Takelac 9 〇 (polyol-based main agent), / ''Takenate A-3 (isocyanate-based hardening -30-201222930 agent)" two-liquid type (100 parts by weight / 10 parts by weight) adhesive, made a /b/c Laminate. Here, the amount of the adhesive applied was 6 g/m2' in terms of solid content on the B side, and after bonding at B/C, the aging treatment was carried out at 45 ° C for 80 hours. On the A/B/C laminated material, a non-aligned polypropylene film (D) having a breaking strength of 35 μηι of 35 MPa, a breaking elongation of 655%, and a Young's modulus of 4 i5 MPa (made by Toyobo Co., Ltd.)丫161^11!1-(:丁?1146'') is extruded at a melting temperature of 140 °〇 at a thickness of 1 (^111, using a modified polyolefin (manufactured by Mitsui Chemicals, Inc., functional base) The branched modified polypropylene "Adomer QE84(R)" was laminated on the interlayer 'between C and D' as the A/B/C/D laminate of the invention. The characteristics are shown in Table 1. [Example 3 1 In addition to Example 30, as a biaxially oriented polyethylene terephthalate film (A), a biaxial alignment having a thickness of 4.5 μm, a breaking strength of 271 MPa, and an elongation at break of 106% was used. In the same manner as in Example 30, a polyethylene terephthalate film ("Lumirror" (registered trademark) F53, manufactured by Toray Industries, Inc.) was used, and the thickness of the aluminum foil (C) was 30 μm, and A/B/C/ was produced in the same manner as in Example 30. D. Laminates. Characteristics are shown in Table 1. [Example 32] In addition to Example 30, instead of biaxial alignment of polyterephthalic acid Ethylene diester film (Α), using a biaxially oriented polyethylene naphthalate film having a thickness of 1 2 μηι, a breaking strength of 3 lOMPa, and an elongation at break of 85 % (Teonex, manufactured by Teijin DuPont Film Co., Ltd.) Q5 1) An A/B/C/D laminate was produced in the same manner as in Example 30 except that the thickness of the aluminum foil (C) was 1 μm. The characteristics are shown in Table 1. -31 - 201222930 [Example 3 3 In addition to Example 25, as a biaxially oriented polyethylene terephthalate film (A), a biaxially oriented polyparaphenylene having a thickness of 16 μm, a breaking strength of 285 MPa, and an elongation at break of 125% was used. Ethylene diacetate film (Teigi η T et 〇r ο n F i 1 m '' G 2) made by Teijin DuPont Film Co., Ltd. 'The thickness of the foil (c) is 1 > μηι, In the same manner as in Example 30, an A/B/C/D laminate was produced. The characteristics are shown in Table 1. [Example 34] In addition to the biaxial alignment polyethylene terephthalate film in Example 30 (Α), using a para-type aromatic polyamide with a thickness of 4.5 μm, a breaking strength of 480 MPa, and an elongation at break of 80% A/B/C/D laminate was produced in the same manner as in Example 30 except that the film was made of "Mictron" (registered trademark) Gq manufactured by Toray Industries, Inc., and the thickness of the aluminum town was ΙΟμπι. The characteristics are shown in Table 1. [Example 35] Except for Example 30, as the polypropylene film (D), an unoriented polypropylene having a thickness of 40 μm, a breaking strength of 33 MPa, an elongation at break of 57%, and a Young's modulus of 3 80 MPa was used. In the same manner as in Example 3, except for the film (Pylenmm-CTPUM, manufactured by Toyobo Co., Ltd.), an A/B/C/D laminate was produced. The characteristics are shown in Table 1. [Example 36] In addition to Example 30, as the polypropylene film (D), an unoriented polypropylene film having a thickness of 37 MPa'" elongation of 73% by weight and a Young's modulus of 50 GMPa was used (Toyo Textile Co., Ltd. limited) In addition to the company's "Pyienfnm-CTP1147,", the A/B/C/D laminate was produced in the same manner as the implementation of "Life". The characteristics are shown in the table! in. -32-201222930 [Example 37] In addition to Example 30, as the polypropylene film (d), a thickness of 80 μηι, a breaking strength of 37 MPa, an elongation at break of 730%, and a Young's modulus of 500 MPa were used. An A/B/C/D laminate was produced in the same manner as in Example 30 except that the non-aligned polypropylene film (Pylenfilm-CT P1 147 manufactured by Toyobo Co., Ltd.) was used. The characteristics are shown in Table 1. [Example 38] Except for Example 30, as a polypropylene film, a non-alignment having a thickness of 25 μm, a breaking strength of 40 MPa, an elongation at break of 480%, and a Young's modulus of 500 Å P a was used. An A/B/C/D laminate was produced in the same manner as in Example 30 except that a polyacryl film ("P y丨enfi 1 m - CTP 1 1 8 1" manufactured by Toyobo Co., Ltd.) was used. The characteristics are shown in Table 1. [Example 39] An A/B/C/D laminate was produced in the same manner as in Example 30 except that the thickness of the interlayer of the modified polyolefin was changed to 30 μm. The characteristics are shown in Table 1. [Example 4 0] In addition to the modified polyolefin in Example 30, it was replaced with an adhesive polyethylene (functional graft-modified polyethylene) "Adomer ΝΕ 827" manufactured by Mitsui Chemicals, Inc., and the interlayer thickness was A/B/C/D laminates were prepared in the same manner as in the case of 30 μm. The characteristics are shown in Table 1. [Example 4 1] In addition to the modified polyolefin, the modified polyolefin was replaced by an ethylene-vinyl acetate copolymer "Evaflex EV550" manufactured by Mitsui & DuPont POLYCHEMICAL Co., Ltd., and the thickness of the interlayer was 4 〇 μιη. Similarly, A/B/C/D laminates were produced. The characteristics are shown in Table 1. -33- 201222930

[實施例4 2 J 除了於實施例3 0中,作為改性聚烯烴’換成住友化 學月史"ί八右 77有限公司製特殊乙烯系共聚物(乙烯/甲基丙烯酸 酯二甲其I κ 土内婦酸醋/丙稀酸曱g旨=7〇/3/27wt%)“Bondfast L 溶喊溫度為l〇5°C以外,同樣地作成A/B/C/D積層 材特性係顯示於表1中。[Example 4 2 J In addition to Example 30, a modified polyolefin was replaced with a special ethylene copolymer made by Sumitomo Chemical History " ί八右77 Ltd. (ethylene/methacrylate) I κ 内 妇 丙 丙 丙 旨 旨 旨 ============================================================================================== The system is shown in Table 1.

[貫施例4 3 J 除了於貫施例3 〇中’將改性聚烯煙換成東洋紡績股 '有限A司製聚浠烴用熱溶性黏著劑‘‘ T 〇 y 〇 t a c Μ 1 0 0,,, 炫融溫度為160°C以外,同樣地作成A/B/C/D積層材。 特性係顯示於表1中。 [貫施例44] 除了於實施例30中,將改性聚烯烴換成三菱化學股 份有限公司製聚丙烯系黏著性樹脂(官能基接枝改性聚 内烯“Modic P553A”),熔融溫度為168t,夾層厚度為 5〇μπι以外’同樣地作成a/b/C/D積層材。特性係顯示於 表1中。 [實施例4 5 ] 除了於實施例3 0中’作為改性聚烯烴,使用三菱化 學股份有限公司製聚丙烯系黏著性樹脂(官能基接枝改 性聚丙烯“Modie Ρ5 5 3 Α”)’熔融溫度為1681,夾層厚度 為 60 μχη 以外,同樣地作成a/b/c/d積層材。特性係顯 示於表1中。 [實施例46] -34- 201222930 除了於實施例30中’作為改性聚烯烴,使用三菱化 學股伤有限公司製聚丙烯系黏著性樹脂(官能基接枝改 性聚丙烯“M〇dicp553A,’),熔融溫度為168。〇,夾層厚度 為6μηι以外’同樣地作成A/B/C/D積層材。特性係顯示 於表1中。 [實施例47] 除了於貫施例3 0中’作為改性聚稀烴,使用三菱化 學股份有限公司製低密度線狀聚乙烯系黏著性樹脂(官 能基接枝改性聚乙烯“Modic M502”),熔融溫度為124t 以外’同樣地作成A/B/C/D積層材。特性係顯示於表i 中 〇 [實施例48] 除了於貫施例30中’在A/B/C積層材與D之間, 疊合厚度30μπι的改性聚丙烯薄膜(TOHCELLO股份有限 公司製“Adomerfilm QE-060C”),以輥溫度15〇。〇、輥壓 力30kg/cm、輸送速度20m/分鐘,藉由熱積層法來熱壓 黏,作成A / B / C / D積層材。特性係顯示於表1中。 [實施例49] 除了於實施例30中’铭箱(C)的厚度成為7μπ1以外 ,與實施例30同樣地’作成A/B/C/D積層材。特性係顯 示於表1中。 [實施例50] 除了於實施例30中,鋁箱(C)的厚度成為40μιη以外 ,與實施例30同樣地,作成A/B/C/D積層材。特性係顯 示於表1中。 -35- 201222930 [實施例5 1 ] 藉由乾積層法’對厚度25μιη、斷裂強度為i65MPa 、斷裂伸長度為215%的二軸配向聚對苯二甲酸乙二酯薄 膜(A)(帝人杜邦薄膜股份有限公司製“TefleX,,FT3)與厚 度15μΙΏ、斷裂強度為l〇3MPa、斷裂伸長度為398%的無 配向尼龍6薄膜(B)(東麗薄膜加工股份有限公司製「 Ray fan」(s主冊商標)N〇 14〇1),使用三井化學聚胺曱酸 酯股份有限公司製的“Takelac A-91〇(多元醇系主劑 )/ T ake na t e A - 3 (異氰酸酯系硬化劑)’’二液型(j⑼重量 份/10重量份)黏著劑,作為A/B積層材。此處,黏著劑 塗布里以固體成分計在A側為5g/m2,於A/B貼合後, 進行40 C、72小時的熟化處理。 藉由乾積層法,疊合A/B積層材、厚度4〇μιη的鋁 /# (C)(住輕銘ν白股份有限公司製‘‘ ν e s p a,,8 〇 2 1)、Β與C ’使用二井化學聚胺甲酸酯股份有限公司製的“Takelac A-910(多元醇系主劑),’/“Takenate A_3(異氰酸酯系硬化 劑)”二液型(100重量份/10重量份)黏著劑,作成A/B/c 積層材。此處黏著劑塗布量係在B側以固體成分計為 6g/m ,於B/C貼合後,進行45°C、80小時的熟化處理 〇 於A/B/C積層材上,將厚度70μιη的斷裂強度為 35MPa、斷裂伸長度為655%、揚氏模數為415Mpa的無 配向聚丙烯薄膜(D)(東洋紡績股份有限公司製 Pylenfilm-CT P1 146”)在 140°C 的熔融溫度,以 ι〇μπι 的 厚度壓出,使用改性聚烯烴(三井化學股份有限公司製, -36- 201222930 官能基接枝改性聚丙烯“Adomer QE840”)於c與D之間 的夾層,進行積層,作成本發明的Α/Β/C/D積層材。特 性係顯示於表1中。 [實施例52] 除了於實施例5 1中’作為二軸配向聚對苯二曱酸乙 二酯薄膜(A),使用厚度50)11111、斷裂強度為195MPa、斷 裂伸長度為190%的二軸配向聚對苯二甲酸乙二醋薄膜( 帝人杜邦薄膜股份有限公司製“Teflex” FT3)以外,與實 施例5 1同樣地,作成A/B/C/D積層材。特性係顯示於表 1中。 [實施例5 3 ] 除了於實施例5 1中,作為二軸配向聚對苯二甲酸乙 二酯薄膜(A),使用厚度50μπι、斷裂強度為195MPa、斷 裂伸長度為1 90%的二軸配向聚對苯二曱酸乙二酯薄膜( 帝人杜邦薄膜股份有限公司製“Teflex” FT3),鋁箔(C)的 厚度為1 Ομηι以外,與實施例5 1同樣地,作成A/B/C/D 積層材。特性係顯示於表1中。 [實施例54] 除了於實施例5 1中,作為聚丙稀薄膜(D ),使用厚 度40μιη、斷裂強度為33Mpa、斷裂伸長度為570%、楊 氏模數3 80MPa的無配向聚丙烯薄膜(東洋紡績股份有限 公司製“Pylenfilm-CT P1153”)以外,與實施例51同樣地 ’作成A/B/C/D積層材。特性係顯示於表1中。 [實施例5 5 ] -37- 201222930 除了於實施例5 1中,作為聚丙烯薄膜(D),使用厚 度100 μιη、斷裂強度為37 MPa、斷裂伸長度為73〇%、楊 氏模數為5 0 0 Μ P a的無配向聚丙烯薄膜(東洋纺績股份有 限公司製“Pylenfilm-CTP1147”)以外,與實施例51同樣 地,作成A/B/C/D積層材。特性係顯示於表i中。 [實施例56] 除了於實施例5 1中,作為聚丙烯薄膜(D),使用厚 度80μηι、斷裂強度為37MPa、斷裂伸長度為73〇%、揚 氏模數為5 0 0 Μ P a的無配向聚丙烯薄膜(東洋紡績股份有 限公司製”Pylenfilm-CT P1147,,)以外,與實施例51同樣 地,作成A/B/C/D積層材。特性係顯示於表1中。 [實施例57] 除了於實施例5 1中,作為聚丙烯薄膜(D),使用厚 度25μηι、斷裂強度為40MPa、斷裂伸長度為480%、祖 氏模數為5 0 0 Μ P a的無配向聚丙烯薄膜(東洋紡績股彳分_ 限公司製“Pylenfilm-CT P1181”)以外,與實施例η □ |aJ樣 地,作成A/B/C/D積層材。特性係顯示於表1中。 [實施例58] 除了於實施例5 1中,改性聚烯烴的夾層之厚度成為 3 0μιη以外,同樣地作成A/B/C/D積層材。特性係顯$ & 表1中。 [實施例59] 除了於實施例5 1中,作為改性聚烯烴,換成二| 學股份有限公司製黏著性聚乙烯(官能基接枝改性聚乙 烯)“Adomer ΝΕ8 2 7”,夾層厚度為30μπι以外,同樣 L作 成A/B/C/D積層材。特性係顯示於表1中。 -38- 201222930 [實施例60] 除了於實施例5 1中,作為改性聚烯烴,換成三井· 杜邦· POLYCHEMICAL股份有限公司製乙烯•醋酸乙 烯酯共聚物“Evaflex EV550”,夾層厚度為40μηι以外, 同樣地作成A/B/C/D積層材。特性係顯示於表1中。 [貫施例6 1 ] 除了於實施例5 1中,作為改性聚烯烴,換成住友化 學股份有限公司製特殊乙烯系共聚物(乙烯/甲基丙烯酸 嗤二甲基丙烯酸酯/丙烯酸甲酯=7〇/3/27wt%)“Bondfast 7L”,熔融溫度為105。〇以外,同樣地作成a/B/C/D積層 材。特性係顯示於表1中。 [實施例6 2 ] 除了於實施例5 1中,將改性聚烯烴換成東洋紡績股 份有限公司製聚烯烴用熱熔性黏著劑“Toyotac M100”, 炫融溫度為160。〇以外,同樣地作成A/B/C/D積層材。 特性係顯示於表1中。 '[實施例6 3 ] 除了於實施例5 1中,將改性聚烯烴換成三菱化學股 份有限公司製聚丙烯系黏著性樹脂(官能基接枝改性聚 丙烯“Modic P5 5 3 A”),熔融溫度為168°C,夾層厚度為 5〇μπι以外’同樣地作成a/B/C/D積層材。特性係顯示於 表1中。 [實施例64] 除了於實施例5 1中,作為改性聚烯烴,使用三菱化 學股份有限公司製聚丙烯系黏著性樹脂(官能基接枝改 -39- 201222930 性聚丙烯“M〇diCP5 5 3 A,,),熔融溫度為i68t:,夾層厚度 為60μιη以外,同樣地作成A/B/c/D積層材。特性係顯 示於表1中。 [實施例65] 除了於貫施例5 1中,作為改性聚烯烴,使用三菱化 學股份有限公司製聚丙烯系黏著性樹脂(官能基接枝改 性聚丙烯“Modic P5 53A”),熔融溫度為168t:,夾層厚度 為6μπι以外’同樣地作成A/B/C/D積層材。特性係顯示 於表1中。 [實施例66] 除了於實施例5 1中,作為改性聚烯烴,使用三菱化 學股份有限公司製低密度線狀聚乙烯系黏著性樹脂(官 能基接枝改性聚乙烯“Modic Μ502”),熔融溫度為i24°C 以外,同樣地作成A/B/C/D積層材。特性係顯示於表1 中。 [實施例67] 除了於實施例51中’在A/B/C積層材與D之間’ 疊合厚度 30μπι的官能基接枝改性聚丙烯薄膜 (TOHCELLO 股份有限公司製 “Adomerfilm QE-060C”)’ 以輥溫度150Ό、輥壓力30kg/cm、輸送速度20m/分鐘’ 藉由熱積層法來熱壓黏’作成A/B/C/D積層材。特性係 顯示於表1中。 [實施例68] 除了於實施例5 1中’銘羯(C)的厚度成為7μπι以外 ,與實施例5 1同樣地’作成A/B/C/D積層材。特性係顯 示於表1中。 -40- 201222930 [實施例69] 除了於實施例51中’銘结(C)的厚度成為8〇μηι以外 ,與實施例51同樣地,作成A/B/C/D積層材。特性係 示於表1中。 ' …[Continuous Example 4 3 J In addition to the application of Example 3 〇, the modified polyene smoke was replaced by the Toyo Textiles Co., Ltd. 'The limited A system of hot-melt adhesive for polyfluorene hydrocarbons'' T 〇y 〇tac Μ 1 0 0,,, A/B/C/D laminate was produced in the same manner except that the temperature was 160 °C. The characteristics are shown in Table 1. [Example 44] In the same manner as in Example 30, the modified polyolefin was replaced with a polypropylene-based adhesive resin (functional graft-modified polyene) "Modic P553A" manufactured by Mitsubishi Chemical Corporation, melting temperature. A/b/C/D laminate was formed in the same manner as 168t and the interlayer thickness was 5〇μπι. The characteristics are shown in Table 1. [Example 4 5] In addition to the modified polyolefin in Example 30, a polypropylene-based adhesive resin (functionalized graft-modified polypropylene "Modie Ρ 5 5 3 Α") manufactured by Mitsubishi Chemical Corporation was used. A/b/c/d laminate was produced in the same manner except that the melting temperature was 1681 and the interlayer thickness was 60 μχη. The characteristics are shown in Table 1. [Example 46] -34-201222930 In addition to the modified polyolefin in Example 30, a polypropylene-based adhesive resin (functional graft-modified polypropylene "M〇dicp553A, manufactured by Mitsubishi Chemical Co., Ltd.) was used. '), the melting temperature was 168. The thickness of the interlayer was 6 μm, and the A/B/C/D laminate was formed in the same manner. The characteristics are shown in Table 1. [Example 47] Except in Example 30 'As a modified polyolefin, a low-density linear polyethylene-based adhesive resin (functional-based graft-modified polyethylene "Modic M502") manufactured by Mitsubishi Chemical Corporation was used, and the melting temperature was 124 t. /B/C/D laminate. The characteristics are shown in Table i [Example 48] except for the modification of the thickness of 30 μm between the A/B/C laminate and D in Example 30 A polypropylene film ("Adomerfilm QE-060C" manufactured by TOHCELLO Co., Ltd.) was heat-pressed by a heat lamination method at a roll temperature of 15 Torr, a roll pressure of 30 kg/cm, and a transfer speed of 20 m/min. B / C / D laminate. The characteristics are shown in Table 1. [Example 49] Except for implementation In the same manner as in Example 30, the A/B/C/D laminate was produced in the same manner as in Example 30, and the characteristics are shown in Table 1. [Example 50] Except for Example 30, except that the thickness of the "case" (C) was changed to 7 μπ. In the same manner as in Example 30 except that the thickness of the aluminum box (C) was 40 μm, an A/B/C/D laminate was produced. The characteristics are shown in Table 1. -35 - 201222930 [Example 5 1] A biaxially oriented polyethylene terephthalate film (A) having a thickness of 25 μm, a breaking strength of i65 MPa, and an elongation at break of 215% by dry-lamination method (TefleX, FT3, manufactured by Teijin DuPont Film Co., Ltd.) Non-aligned nylon 6 film (B) having a thickness of 15 μm, a breaking strength of l〇3 MPa, and an elongation at break of 398% ("Ray fan" (s main book trademark) manufactured by Toray Film Processing Co., Ltd. N〇14〇1 ), "Takelac A-91 〇 (polyol-based main agent) / T ake na te A - 3 (isocyanate-based hardener)" by the Mitsui Chemical Polyamine Ethyl Copolymer Co., Ltd.'' two-liquid type (j (9) weight 10 parts by weight of the adhesive, as an A/B laminate. Here, the adhesive is coated on the A side as a solid component. 5g/m2, after A/B bonding, 40 C, 72 hours of aging treatment. By dry layering method, superimposed A/B laminated material, thickness 4 〇μηη of aluminum / # (C) 'ν spa spa spa 股份有限公司 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 T T T T T T T T T T T T T T T T T T T T T T T T T T T T T T T / "Takenate A_3 (isocyanate-based curing agent)" two-component type (100 parts by weight / 10 parts by weight) of an adhesive to form an A/B/c laminate. Here, the amount of the adhesive applied is 6 g/m in terms of solid content on the B side, and after bonding at B/C, the composition is aged at 45 ° C for 80 hours, and the thickness is applied to the A/B/C laminate. A 70 μm η unbonded polypropylene film (D) (Pylenfilm-CT P1 146 manufactured by Toyobo Co., Ltd.) having a breaking strength of 35 MPa, an elongation at break of 655%, and a Young's modulus of 415 MPa, at a melting temperature of 140 ° C It is extruded at a thickness of ι〇μπι, using a modified polyolefin (manufactured by Mitsui Chemicals, Inc., -36-201222930 functional graft-modified polypropylene "Adomer QE840") in a sandwich between c and D. The laminate was used as the Α/Β/C/D laminate of the invention. The characteristics are shown in Table 1. [Example 52] In addition to the biaxial alignment of polyethylene terephthalate in Example 51 Film (A), except for a biaxially oriented polyethylene terephthalate film (Teflex FT3 manufactured by Teijin DuPont Film Co., Ltd.) having a thickness of 5011111, a breaking strength of 195 MPa, and an elongation at break of 190%. In the same manner as in Example 51, an A/B/C/D laminate was produced. The characteristics are shown in Table 1. [Example 5 3] In addition to Example 52, as the biaxially-oriented polyethylene terephthalate film (A), a two-axis having a thickness of 50 μm, a breaking strength of 195 MPa, and an elongation at break of 1 90% was used. A/B/C was prepared in the same manner as in Example 51 except that the polyethylene terephthalate film (Teflex FT3, manufactured by Teijin DuPont Film Co., Ltd.) and the thickness of the aluminum foil (C) were 1 Ομηι. /D Laminates. Characteristics are shown in Table 1. [Example 54] In Example 51, as the polypropylene film (D), a thickness of 40 μm, a breaking strength of 33 MPa, and an elongation at break of 570% were used. A non-aligned polypropylene film having a Young's modulus of 3 80 MPa (Pylenfilm-CT P1153 manufactured by Toyobo Co., Ltd.) was used to produce an A/B/C/D laminate in the same manner as in Example 51. The characteristics are shown in [Example 5 5 ] -37- 201222930 In addition to Example 51, as a polypropylene film (D), a thickness of 100 μm, a breaking strength of 37 MPa, an elongation at break of 73%, and a yang were used. Non-aligned polypropylene film with a modulus of 500 Μ P a (Toyo Textile Co., Ltd. has An A/B/C/D laminate was produced in the same manner as in Example 51 except for the "Pylenfilm-CTP1147" manufactured by Konica Minolta Co., Ltd. The characteristics are shown in Table i. [Example 56] Except in Example 51, As the polypropylene film (D), an unoriented polypropylene film (manufactured by Toyobo Co., Ltd.) having a thickness of 80 μm, a breaking strength of 37 MPa, a breaking elongation of 73% by weight, and a Young's modulus of 500 Å P a was used. In the same manner as in Example 51 except for Pylenfilm-CT P1147, a), an A/B/C/D laminate was produced. The characteristics are shown in Table 1. [Example 57] Except for Example 51, as the polypropylene film (D), a thickness of 25 μm, a breaking strength of 40 MPa, an elongation at break of 480%, and a modulus of Zu: 500 Μ P a were used. An A/B/C/D laminate was produced in the same manner as in Example η □ |aJ except for the oriented polypropylene film (Pylenfilm-CT P1181 manufactured by Toyobo Co., Ltd.). The characteristics are shown in Table 1. [Example 58] An A/B/C/D laminate was produced in the same manner as in Example 51 except that the thickness of the interlayer of the modified polyolefin was changed to 30 μm. The feature is shown in $&1. [Example 59] In the same manner as in Example 51, as a modified polyolefin, an adhesive polyethylene (functional graft-modified polyethylene) "Adomer ΝΕ 8 2 7" made of Erzhi Co., Ltd. was laminated. In the same manner as the thickness of 30 μm, the same L was used as the A/B/C/D laminate. The characteristics are shown in Table 1. -38-201222930 [Example 60] In the same manner as in Example 51, the modified polyolefin was replaced with an ethylene-vinyl acetate copolymer "Evaflex EV550" manufactured by Mitsui & DuPont POLYCHEMICAL Co., Ltd., and the interlayer thickness was 40 μm. In the same manner, A/B/C/D laminates were produced in the same manner. The characteristics are shown in Table 1. [Example 6 1] In addition to the modified polyolefin in Example 51, a special ethylene copolymer (ethylene/methacrylic acid bismuth methacrylate/methyl acrylate) manufactured by Sumitomo Chemical Co., Ltd. was replaced. = 7 〇 / 3 / 27 wt%) "Bondfast 7L", melting temperature is 105. A/B/C/D laminates were prepared in the same manner as 〇. The characteristics are shown in Table 1. [Example 6 2] In the same manner as in Example 51, the modified polyolefin was changed to "Toyotac M100" which is a hot-melt adhesive for polyolefins manufactured by Toyobo Co., Ltd., and the melting temperature was 160. A/B/C/D laminates were produced in the same manner except for ruthenium. The characteristics are shown in Table 1. '[Example 6 3 ] In addition to Example 51, the modified polyolefin was replaced with a polypropylene-based adhesive resin (functionalized graft-modified polypropylene "Modic P5 5 3 A" manufactured by Mitsubishi Chemical Corporation). The a/B/C/D laminate was formed in the same manner, except that the melting temperature was 168 ° C and the thickness of the interlayer was 5 μm. The characteristics are shown in Table 1. [Example 64] In addition to the modified polyolefin, a polypropylene-based adhesive resin manufactured by Mitsubishi Chemical Corporation was used as a modified polyolefin (functionalized graft-modified -39-201222930 polypropylene "M〇diCP5 5 3 A,,), the melting temperature was i68t:, and the interlayer thickness was 60 μm, and the A/B/c/D laminate was similarly produced. The characteristics are shown in Table 1. [Example 65] Except for Example 5 In the case of the modified polyolefin, a polypropylene-based adhesive resin (functional-based graft-modified polypropylene "Modic P5 53A") manufactured by Mitsubishi Chemical Corporation was used, and the melting temperature was 168 t: and the interlayer thickness was 6 μm. The A/B/C/D laminate was produced in the same manner. The characteristics are shown in Table 1. [Example 66] In addition to Example 51, as a modified polyolefin, a low density line manufactured by Mitsubishi Chemical Corporation was used. A polyethylene-based adhesive resin (functional-based graft-modified polyethylene "Modic Μ 502"), and an A/B/C/D laminated material was produced in the same manner except that the melting temperature was i24 ° C. The characteristics are shown in Table 1. [Example 67] Except in Example 51 'in A/B/C laminated material A functional group graft-modified polypropylene film ("Adomerfilm QE-060C" manufactured by TOHCELLO Co., Ltd.) having a thickness of 30 μm is laminated with D at a roll temperature of 150 Torr, a roll pressure of 30 kg/cm, and a conveying speed of 20 m/min. The A/B/C/D laminate was thermally pressed by a thermal lamination method. The characteristics are shown in Table 1. [Example 68] Except that in Example 51, the thickness of the mold (C) was In the same manner as in Example 51, except for 7 μm, the A/B/C/D laminate was produced. The characteristics are shown in Table 1. -40 - 201222930 [Example 69] In addition to Example 51, "Ming knot (C In the same manner as in Example 51, an A/B/C/D laminate was produced in the same manner as in Example 51. The characteristics are shown in Table 1. ...

[實施例70J 作為二轴配向聚對苯二曱酸乙二酯薄膜(Α),使用 重量%的聚對苯二曱酸乙二酯、6〇重量%當作聚酯的 間苯二甲酸10莫耳共聚合聚對苯二甲酸丁二酯,調整至 含有0.012重量%的平均粒徑12_之球狀矽石粒子。將 聚合物碎片在150。〇真空乾燥3小時後,供應給單軸壓出 機’由通常的喷嘴吐出後,邊施加靜電邊在鏡面冷卻鼓 上冷卻固化而得到未配向薄膜。藉由非黏性聚矽氧輥( 硬度73。),以7〇。。的延伸溫度’將此未配向薄膜在長度 方向中延伸2·0倍後,於拉幅機内在1 lot:於寬度方向令 L伸2.0彳。,接著以1 § 〇〇的薄膜溫度,邊熱處理5秒邊 在寬度方向中鬆弛4% ’而得到厚度3〇μιη、斷裂強度為 lOIMPa、断裂伸長度為189%的二軸配向聚對苯二曱酸 乙二醋薄膜。其它係與實施例5 1同樣地,作成a/b/C/D 積層材。特性係顯示於表1中。 [實施例7 1 ] 除了於貫施例5 1中’作為二軸配向聚對苯二甲酸乙 二S旨薄膜(A) ’使用厚度50μηι、斷裂強度為25〇MPa、斷 裂伸長度為178%的二軸配向聚對苯二曱酸乙二酯薄膜( 東麗股份有限公司製「Lumirror」(註冊商標)F99)以外, 與實施例5 1同樣地’作成A/B/C/D積層材。特性係顯示 於表1中。 • 41 - 201222930 [實施例7 2 ] 除了於實施例5 1中,作為二軸配向聚對苯二甲酸乙 一醋薄膜(A),使用厚度5〇μΓη、斷裂強度為232Mpa、斷 裂伸長度為1 82%的二軸配向聚對苯二曱酸乙二酯薄膜( 東麗股份有限公司製「Lumirror」(註冊商標)S56)以外, 與實施例5 1同樣地’作成A/B/C/D積層材。特性係顯示 於表1中。 [比較例1 ] 於實施例1中,作為尼龍薄膜(B),使用配向尼龍薄 膜(東洋紡績股份有限公司製二軸配向薄膜“Hardenfilm N1 100”)。其它係與實施例1同樣地,作成A/B/C/D積層 材。特性係顯示於表1中。 [比較例2] 除了於實施例1中,不使用改性聚稀烴,代替地使 用宇部興產股份有限公司製高密度聚乙烯“UBE Polyethylene L7 1 9”,溶融溫度為1 〇8°C以外,同樣地作 成A/B/C/D積層材。特性係顯示於表1中。 [比較例3 ] 於實施例1中,疊合A/B/C積層材與無配向聚丙烯 薄膜(D)(東洋紡績股份有限公司製“pylenfilm-CT P 1 146”)、C與D,藉由乾積層.法’使用三井化學聚胺曱 酸酯股份有限公司製的“Takelac A-910(多元醇系主劑 )T a k e n a t e A - 3 (異氰酸酿糸硬化劑)’’二液型(1 〇 〇重量 份/10重量份)黏著劑,作成a/b/c/d積層材。此處’黏 著劑塗布量係在C側以固體成分计為6g/m ,於C/D貼 -42 - 201222930 合後,進行45°C、80小時的熟化處理。其它係與實施例 1同樣地,作成A/B/C/D積層材。特性係顯示於表i中 〇 [比較例4 ] 於實施例1中,作為聚丙烯薄膜(D),使用厚度6〇μιη 的配向聚丙烯薄膜(東麗股份有限公司製二軸配向聚丙 烯薄膜「Torayfan」(註冊商標)2500Η)β其它係與實施例 1同樣地,作成A/B/C/D積層材。無法熱封,無法作成 袋子,無法作成二次電池用容器。 [比較例5 ] 除了於貫施例1中,作為聚丙烯薄膜(D),使用厚度 40μηι、斷裂強度為38MPa、斷裂伸長度為楊氏 模數為630MPa的無配向聚丙烯薄膜(東洋紡績股份有限 公司製“Pylenfilm-CT PlUl,,)以外,與實施例i同樣地 ’作成A/B/C/D積層材。特性係顯示於表1中。 [比較例6 ] 於實施例1中,作為D,使用厚度6〇μηι的斷裂強 度為47MPa、斷裂伸長度為635%、楊氏模數為630MPa 的無配向之聚丙稀薄膜東麗薄膜加工股份有限公司 製「Torayfan」(註冊商標)n〇33〇1)。其它係與實施例1 同樣地,作成A/B/C/D積層材。特性係顯示於表!中。 [比較例7] 於實施例1中’不使用聚酯薄膜(A)。不作成A/B積 層材’其它係與實施例1同樣地,作成B/c/D積層材。 特性係顯示於表1中。 -43- 201222930 [比較例8 ] 於實施例1中,作為D,使用厚度40 μηι的斷裂強 度為38MPa、斷裂伸長度為500%、楊氏模數5 8 5MPa的 無配向之聚丙烯薄膜(D)(東洋紡績股份有限公司製 “Pylenfilm_CT Pll28”)。其它係與實施例1同樣地,作 成A/B/C/D積層材。特性係顯示於表1中。 [比較例9 ] 於實施例1中,疊合A/B積層材與C ' A與C,同 樣地進行實施例丨的黏著劑、黏著劑塗布量、熟化處理 ’作成B/A/C積層材。然後與實施例1同樣地,作成 B/A/C/D積層材。特性係顯示於表1中。 [比較例10] 藉由乾積層法’對厚度12μιη、斷裂強度為240MPa 、斷裂伸長度為1 1 8 %的二軸配向聚對苯二曱酸乙二酯薄 膜(A)(東麗月又份有限公司製「Lumirr〇r」(註冊商標)p6〇) 與厚度40μπι的鋁箔(c)(住輕鋁箔股份有限公司製 “Vespa” 8021) ’使用三井化學聚胺甲酸酯股份有限公司 製的 “Takelac A-910(多元醇系主劑丁akenate A_3(異 氰酸酯系硬化劑),,二液型(丨〇〇重量份/丨〇重量份)黏著劑 ,作成A/C積層材。此處黏著劑塗布量係在A側以固體 成分計為6g/m2,於A/C貼合後,進行45t、80小時的 熟化處理。 藉由乾積層法,對厚度15μπι、斷裂強度為1〇3MPa 、斷裂伸長度為398%的無配向尼龍ό薄膜(b)(東麗薄膜 加工股份有限公司製「Rayfan」(註冊商標)NO 1401)與 -44 - 201222930 厚度70 μιη的斷裂強度為35 MPa、斷裂伸長度為655°/。、 杨氏模數為4 1 5 Μ P a的無配向聚丙稀薄膜(D)(東洋紡績 股份有限公司製“Pylenfilm_CT P1 146”),使用三井化學 聚胺曱酸酯股份有限公司製的“Takelac A-9 1 0(多元醇系 主劑)”/”Takenate A-3(異氰酸酯系硬化劑),’二液型(100 重量份/10重量份)黏著劑,作成B/D積層材。此處黏著 劑塗布量以固體成分計在B側為5g/m2,於B/D貼合後 ,進行40°C、72小時的熟化處理。 將A/C積層材與b/d積層材在140°C的熔融溫度, 以1 0 μιη的厚度壓出,使用改性聚烯烴(三井化學股份有 限公司製,官能基接枝改性聚丙烯“Adomer QE840”)於 C與B之間的夾層’進行積層,作成a/C/B/D積層材。 特性係顯示於表1中。 [比較例1 1 ] 藉由乾積層法’對厚度7〇μηι的斷裂強度為35Mpa 、斷裂伸長度為655°/。、揚氏模數為415MPa的無配向聚 丙稀薄膜(D)(東洋纺績股份有限公司製“pyienfilm_CT P1146 )與厚度15μπι、斷裂強度為i〇3Mpa、斷裂伸長度 為j98 /。的無配向尼龍6薄膜(B)(東麗薄膜加工股份有限 公司製「Rayfan」(註冊商標)NO 1401),使用三井化學 聚胺甲酸醋股份有限公司製的“Take丨μ A-9i〇(多元醇系 主劑)/ Takenate A-3(異氰酸酯系硬化劑),,二液型(1〇〇 重里伤/ίο重置份)黏著劑,作成d/b積層材。此處黏著 月J k布里以固體成分計在B側為5g/m2,於貼合後 ,進灯40 C、72小時的熟化處理。 -45- 201222930 藉由乾積層法,疊合D/B積層材、厚度40μιη的铭 箔(C)(住輕鋁箔股份有限公司製”Vespa” 8021)、Β與C ’使用三井化學聚胺甲酸酯股份有限公司製的’’Takelac A-910(多元醇系主劑),’/‘‘Takenate A-3(異氰酸酯系硬化 劑)”二液型(100重量份/10重量份)黏著劑,作成D/B/C 積層材。此處黏著劑塗布量係在B側以固體成分計為 6g/m2,於D/B/C貼合後,進行45°C、80小時的熟化處 理。 於D/B/C積層材上,將厚度 12μιη、斷裂強度為 24 0MPa、斷裂伸長度為1 18%的二軸配向聚對苯二曱酸乙 二酯薄膜(A)(東麗股份有限公司製「Lumirror」(註冊商標 )P60)在140°C的炫融溫度,以ΙΟμπι的厚度壓出,使用改 性聚烯烴(三井化學股份有限公司製,官能基接枝改性聚 丙烯“Adomer QE84〇”)於C與Α之間的夹層,進行積層, 作成A/C/B/D積層材。特性係顯示於表1中。 [比較例12] 於實施例3 0中,作為尼龍6薄膜(β ),使用配向尼 龍6薄膜(東洋紡績股份有限公司製二軸配向薄膜 “Hardenfilm N.1100’’)。其它係與實施例3〇同樣地,作 成A/B/C/D積層材。特性係顯示於表j中。 [比較例1 3 ] 除了於實施例30中,不使用改性聚烯烴,代替地使 用宇部興產股份有限公司製高密度聚乙烯“υβΕ聚乙稀 L719 ’溶融、’蓋度為108C以外’同樣地作成a/B/C/D積 層材。特性係顯示於表1中。 201222930 [比較例14 ] 於實施例30中,藉由乾積層法,疊合a/b/c積層材 與無配向聚丙烯薄膜(D)(東洋紡績股份有限公司製 “PylenfilmCT PI i46”)、C與D,使用三井化學聚胺曱酸 醋股份有限公司製的“Takelac A_9l〇(多元醇系主劑 )”/“Takenate A-3(異氰酸酯系硬化劑),,二液型(1〇〇重量 份/10重量份)黏著劑’作成A/B/C/D積層材。此處黏著 劑塗布量係在C側以固體成分計為6g/m2,於C/D貼合 後’進行45°C、80小時的熟化處理。其它係與實施例3〇 同樣地,作成A/B/C/D積層材。特性係顯示於表i中。 [比較例15] 於實施例30中,作為聚丙烯薄膜(D),使用厚度6〇μιη 的配向聚丙稀薄膜(東麗股份有限公.司製二軸配向聚丙 稀薄膜「Torayfan」(註冊商標)2500Η)β其它係與實施例 30同樣地,作成A/B/C/D積層材。無法熱封,無法作成 袋子’無法作成二次電池用容器。 [比較例16] 除了於貫施例3 0中,作為聚丙稀薄膜(D ),使用厚 度40μιη、斷裂強度為38MPa、斷裂伸長度為51〇%、揚 氏模數為630MPa的無配向聚丙烯薄膜(東洋紡績股份有 限公司製“Pylenfilm-CT P1111”)以外,與實施例3〇同樣 地’作成A/B/C/D積層材。特性係顯示於表1中。 [比較例17] 於實施例30中,作為D,使用厚度6〇μηι的斷裂強 度為47MPa、斷裂伸長度為635%、揚氏模數為63〇Mpa -47- 201222930 的無配向之聚丙烯薄膜(D)(東麗薄膜加工股份有限公司 製「Torayfan」(註冊商標)NO 3301 )。其它係與實施例 3 0同樣地,作成A / B / C / D積層材。特性係顯示於表1中 [比較例1 8 ] 於實施例30中,不使用聚酯薄膜。不作成a/B 積層材,其它係與實施例30同樣地,作成b/C/D積層材 。特性係顯示於表1中。 [比較例19] 於實施例30中,作為D,使用厚度4〇μιη的斷裂強 度為38MPa、斷裂伸長度為5〇〇%、揚氏模數585Mpa的 無配向之聚丙烯薄膜(D)(東洋紡績股份有限公司製 “Pyunfilm-CT P1128”)。其它係與實施例3〇同樣地,作 成A/B/C/D積層材。特性係顯示於表^中。 [比較例20] 於貝把例30巾’疊合A/B積層材與c、A與同 樣地進行實施们0的黏著劑、黏著劑塗布量、熟化處理 ,作成B/A/C積層材。然後 …'便與貫施例30同樣地,作成 B/A/C/D積層材。特性係顯示於表ι中。 [比較例2 1 ] 藉由乾積層法,對厚声 、斷裂伸長度為118%的二:g -、斷裂強度為27覽3 f 一軸配向聚對笨二曱酸乙二酯薄 膜(A)(東麗 >專勝加工股份有限公司 商標)P375)與厚度25μηι的 、㈣⑽1*」㈡冊 司製“Vespa” 8021),使用::仰住輕1呂猪股份有限公 —井化學聚胺甲酸酯股份有限 -48- 201222930 么司製的Takelac A-91〇(多元醇系主劑),,/“Takenate A-3(異氰酸酯系硬化劑)’’二液型(1〇〇重量份“ο重量份) 黏著劑’作成A/C積層材。此處黏著劑塗布量係在a側 以固體成分計為6g/m2,於A/C貼合後,進行45。(:、80 小時的熟化處理。 藉由乾積層法,對厚度15μπ1、斷裂強度為1〇3MPa 斷裝伸長度A 3 98%的無配向尼龍6薄膜(B)(東麗薄膜 力=工股份有限公司製「Rayfan」(註冊商標)N〇 14〇1)與 厚度7〇μηι的斷裂強度為35MPa、斷裂伸長度為655%、 楊氏模數為415MPa的無配向聚丙烯薄膜(D)(東洋紡績 股份有限公司製“Pylenfilm_CT P1 M6”),使用三井化學 聚胺曱酸酯股份有限公司製的“Takelac A_91〇(多元醇系 主知1丨)/ Takenate A-3(異氰酸酯系硬化劑),’二液型(1〇〇 重量份/10重量份)黏著劑,作成B/D積層材。此處黏著 劑塗布量以固體成分計在B側為5g/m2,於B/D貼合後 ’進行4 0 °C、7 2小時的熟化處理。 將A/C積層材與B/D積層材在i4(TC的熔融溫度, 以ΙΟμιη的厚度壓出,使用改性聚烯烴(三井化學股份有 限公司製,官能基接枝改性聚丙烯“ Ad〇mer qE84〇,,)於 C與B之間的夾層,進行積層,作為A/c/B/D積層材。 特性係顯示於表丨中。 [比較例2 2 ] 藉由乾積層法’對厚度70μιη的斷裂強度為35Mpa 、斷裂伸長度為655%、楊氏模數為415MPa的無配向聚 丙烯/專膜(D)(東洋紡績股份有限公司製,,p y 1 e n f丨丨⑺c τ -49- 201222930 卩1146’’)與厚度1化111、斷裂強度為1〇3^1^、斷裂伸長度 為398%的無配向尼龍6薄膜(B)(東麗薄膜加工股份有限 公司製「Rayfan」(註冊商標)Ν〇 ι4〇1),使用三井化學 聚胺甲酸醋股份有限公司製的“Take丨ac A_91〇(多元醇系 主劑)’’/“Takenate A-3(異氰酸酯系硬化劑),,二液型(100 重3:份/10重量份)黏著劑,作成D/b積層材。此處,黏 著劑塗布量以固體成分計在B侧為5g/m2,於D/B貼合 後’進行4 0 C、7 2小時的熟化處理。 藉由乾積層法,疊合D/B積層材、厚度25μιη的鋁 箔(C)(住輕鋁箔股份有限公司製“Vespa” 8021)、Β與C ’使用三井化學聚胺曱酸酯股份有限公司製的“TakeUc A-910(多元醇系主劑)”/“Takenate A_3(異氰酸酯系硬化 劑)”二液型(1〇〇重量份/1〇重量份)黏著劑,作成D/B/c 積層材。此處黏著劑塗布量係在B側以固體成分計為 6g/m2,於D/B/C貼合後,進行45°C、80小時的熟化處 理〇 於D/B/C積層材上,將厚度6.5μιη、斷裂強度為 275MPa、斷裂伸長度為11 8%的二轴配向聚對苯二曱酸 乙二酯薄膜(A)(東麗股份有限公司製「Lumirror」(註冊 商標)P60)在140C的炼融溫度’以ΙΟμιη的厚度壓出, 使用改性聚烯烴(三丼化學股份有限公司製,“官能基接 枝改性聚丙烯“Adomer QE840”)於C與Α之間的夹層, 進行積層,作成A/c/B/D積層材。特性係顯示於表1中 -50- 201222930 [比較例23] 除了於實施例30中,代替二軸配向聚對苯二甲酸乙 二酯薄膜(A) ’使用厚纟4.5_、斷裂強度為6〇〇Mpa、 斷裂伸長度為50。/。的對位系芳香族聚醯胺薄膜(東麗股 份有限公司製「Mictron」(註冊商標)ML)以外,與實施 例30同樣地,作成A/B/C/D積層材。特性係顯示於表i 中。 [比較例24] 除了於實施例3 0中’作為二輛配向聚對苯二甲酸乙 二醋薄膜(A),使用厚度12μιη、斷裂強度為23 5MPa、、 斷裂伸長度為95 %的二轴配向聚對苯二甲酸乙二酯薄膜 (東洋紡績股份有限公司製“東洋紡Esterfilm E51()(n, 鋁箔(C)的厚度為ΐ〇μπι以外,與實施例3〇同樣地,作成 A/B/C/D積層材。特性係顯示於表1中。 [比較例2 5 ] 除了於實施例3 0中’作為二軸配向聚對苯二曱酸乙 二醋薄膜(Α),使用厚度50μπι、斷裂強度為6〇MPa、斷 裂伸長度為3 6 5 %的·一袖配向聚對笨二曱酸乙二g旨薄膜( 帝人杜邦薄膜股份有限公司製“ T e f 1 e X ρ τ 7,,)以外,與實 施例3 0同樣地’作成A / B / C / D積層材。特性係顯示於表 1中。 [比較例2 6 ] 於實施例5 1中’作為尼龍6薄膜(b),使用配向尼 龍6薄膜(東洋紡績股份有限公司製二軸配向薄膜 “Hardenfilm N1 100”)。其它係與實施例51同樣地,作成 A/B/C/D積層材。特性係顯示於表i中。 -51- 201222930 [比較例27] 於實施例5 1中,不使用改性聚烯烴,代替地使用宇 部興產股份有限公司製高密度聚乙烯“UBE Polyethylene L719”,熔融溫度為l〇8°C以外,同樣地作成A/B/C/D積 層材。特性係顯示於表1中。 [比較例28] 於實施例5 1中,藉由乾積層法,疊合a/B/C積層材 與無配向聚丙烯薄膜(D)(東洋紡績股份有限公司製 Pylenfilm-CT P1 146”)、C與D,使用三井化學聚胺甲酸 ®曰股份有限公司製的“Takelac A-910(多元醇系主劑 )/ Takenate A-3(異氰酸酯系硬化劑)”二液型〇〇〇重量 份/10重量份)黏著劑,作成A/B/C/D積層材。此處黏著 劑塗布里係在C侧以固體成分計為6g/m2,於C/D貼合 後,進行d、80小時的熟化處理。其它係與實施例5 j 同樣地,作成A/B/C/D積層材。特性係顯示於表丄中。 [比較例29] 於實施例51中,作為聚丙烯薄膜(D),使用厚度6〇μιη 的配向聚丙烯薄膜(東麗股份有限公司製二軸配向聚丙 稀薄膜「Torayfan」(註冊商標)25〇〇Η)。其它係與實施例 51同樣地,作成A/B/C/D積層材。無法熱封,無法作成 袋子’無法作成二次電池用容器。 [比較例30] 除了於實施你"1巾,作為聚丙烯薄膜(d),使用厚 度40叫、斷裂強度為38MPa、斷裂伸長度為別%、楊 氏模數為630MPa的無配向聚丙烯薄膜(東洋紡績股份有 -52- 201222930 限公司製”Pylenfilm-CT PI 1 1 1”)以外,與實施例5ι同樣 地,作成A/B/C/D積層材。特性係顯示於表1中。 [比較例3 1 ] 於實施例5 1中’作為D,使用厚度60μηι的斷裂強 度為47MPa、斷裂伸長度為63 5%、楊氏模數為630MPa 的無配向之聚丙烯薄膜(D)(東麗薄膜加工股份有限公司 製「Torayfan」(註冊商標)NO 3301 )。其它係與實施例 5 1同樣地’作成A/B/C/D積層材。特性係顯示於表1中 〇 [t匕較例3 2 ] 於實施例5 1中,不使用聚酯薄膜。不作成a/B 積層材’其它係與實施例5 1同樣地,作成B/C/D積層材 。特性係顯示於表1中。 [比較例3 3 ] 於實施例5 1中,作為〇,使用厚度40 μιη的斷裂強 度為38MPa、斷裂伸長度為5〇〇〇/q、揚氏模數585MPa的 無配向之聚丙烯薄臈(D)(東洋紡績股份有限公司製 ”Pylenfilm-CTP1128”)。其它係與實施例^同樣地,作 成A/B/C/D積層材。特性係顯示於表1中。 [比較例3 4 ] 於實施例51中,疊合A/B積層材與C、A與C,同 樣地進行實施例5 1的黏著劑、黏著劑塗布量、熟化處理 ’作成B/A/C積層材。然後與實施例$ 1同樣地,作成 B/A/C/D積層材。特性係顯示於表工中。 [比較例3 5 ] -53- 201222930 糟由乾積層法,對·厘南Λ c 又25μιη、斷裂強度為165Μ 、斷裂伸長度為⑽的二轴配向聚對苯二甲酸乙二酷薄 Μ (Α)(帝人杜邦薄膜股份有限公司製“Teflex” FT3)斑厚 度4〇μϊη的銘箱(C)(住輕紹落股份有限公司製“ve^a” 8021) ’纟用三井化學聚胺曱酸酯股份有限公司製的 “Takelac A-910(多元醇系主劑),,/“Takenate A 3(里氰酸 I系硬化劑),’二液型(100重量份/1〇重量份)黏著劑,作 成A/C積層#。此處黏著劑塗布量係纟八側以固體成分 計為6g/m2,於A/C貼合後,進行45t、8〇小時的熟化 處理。 藉由乾積層法,對厚度15μπι、斷裂強度為ι〇3Μρ& 斷裂伸長度為398%的無配向尼龍6薄膜(B)(東麗薄膜 加工股份有限公司製「Rayfan」(註冊商標)N〇 “◦㈠與 厚度70μηι的斷裂強度為35MPa、斷裂伸長度為655%、 揚氏模數為415MPa的無配向聚丙烯薄膜(D)(東洋紡績 股份有限公司製“Pylenfilm_CT P1 146,,),使用三井化學 聚胺甲酸酯股份有限公司製的“Takelac A_91〇(多元醇系 主劑)/ Takenate A-3(異氰酸酯系硬化劑),,二液型(1〇〇 重量份/1 0重量份)黏著劑,作成B/D積層材。此處,黏 著劑塗布量以固體成分計在B側為5g/m2,於B/D貼合 後,進行4 0 °C、7 2小時的熟化處理。. 將A/C積層材與β/D積層材在14〇t的熔融溫度, 以1 Ομηι的厚度壓出,使用改性聚烯烴(三井化學股份有 限公司製,官能基接枝改性聚丙烯“Adomer QE840”)於 C與B之間的夾層,進行積層,作成A/C/B/D積層材。 特性係顯示於表1中。 -54 - 201222930 [比較例36] 藉由乾積層法,對厘麻 ΐ厚度70μπι的斷裂強度為35Μρ& 、斷裂伸長度為655%、楊氏模數為415购的無配向聚[Example 70J as a biaxially oriented polyethylene terephthalate film (Α), using wt% of polyethylene terephthalate, and 6 wt% of polyester as isophthalic acid 10 The methane copolymerized polybutylene terephthalate was adjusted to have a spherical vermiculite particle having an average particle diameter of 12% by weight of 0.012% by weight. The polymer fragments are at 150. After drying for 3 hours in a vacuum, the uniaxial extruder was discharged from a normal nozzle, and then cooled and solidified on a mirror cooling drum while applying static electricity to obtain an unaligned film. By a non-adhesive polyfluorene roller (hardness 73.), 7 〇. . The elongation temperature of the unaligned film was extended by 2.0 times in the longitudinal direction, and then stretched by 2.0 Å in the width direction in the tenter. Then, at a film temperature of 1 § ,, while relaxing at 4% in the width direction while heat treatment for 5 seconds, a biaxially oriented polyparaphenylene having a thickness of 3 〇 μηη, a breaking strength of 10 MPa, and an elongation at break of 189% was obtained. A film of bismuth citrate. In the same manner as in Example 51, an a/b/C/D laminate was produced. The characteristics are shown in Table 1. [Example 7 1] In addition to the film of Example 5, 'as a biaxially oriented polyethylene terephthalate film (A)', the thickness was 50 μm, the breaking strength was 25 MPa, and the elongation at break was 178%. In the same manner as in Example 51, except for the film of the polyethylene terephthalate film ("Lumirror" (registered trademark) F99 manufactured by Toray Industries, Inc.), the A/B/C/D laminate was produced. . The characteristics are shown in Table 1. • 41 - 201222930 [Example 7 2 ] In addition to Example 51, as a biaxially oriented polyethylene terephthalate film (A), a thickness of 5 〇μΓη, a breaking strength of 232 MPa, and an elongation at break of 1 were used. An A/B/C/D was created in the same manner as in Example 51 except that 82% of the biaxially-oriented polyethylene terephthalate film ("Lumirror" (registered trademark) S56 manufactured by Toray Industries, Inc.) was used. Laminates. The characteristics are shown in Table 1. [Comparative Example 1] In the first embodiment, a nylon film (a biaxial alignment film "Hardenfilm N1 100" manufactured by Toyobo Co., Ltd.) was used as the nylon film (B). In the same manner as in Example 1, an A/B/C/D laminate was produced. The characteristics are shown in Table 1. [Comparative Example 2] Except that in Example 1, the modified polyolefin was not used, and UBE Polyethylene L7 1 9 made of Ube Industries, Ltd. was used instead, and the melting temperature was 1 〇 8 ° C. In the same manner, A/B/C/D laminates were produced in the same manner. The characteristics are shown in Table 1. [Comparative Example 3] In Example 1, a composite A/B/C laminate and an unoriented polypropylene film (D) ("pylenfilm-CT P 1 146" manufactured by Toyobo Co., Ltd.), C and D, "Takelac A-910 (Polyol based main agent) T akenate A - 3 (isocyanate sputum hardener)"' two liquid made by Mitsui Chemical Polyamine Ethylate Co., Ltd. by dry laminate method Type (1 〇〇 by weight/10 parts by weight) of adhesive to form a/b/c/d laminate. Here, the amount of adhesive applied is 6 g/m on the C side as solid content, at C/D. Post-42 - 201222930 After the combination, the aging treatment was carried out at 45 ° C for 80 hours. In the same manner as in Example 1, an A/B/C/D laminate was produced. The characteristics are shown in Table i [Comparative Example] 4) In the first embodiment, an oriented polypropylene film having a thickness of 6 μm was used as the polypropylene film (D) (two-axis alignment polypropylene film "Torayfan" (registered trademark) 2500 Å manufactured by Toray Industries, Inc.) In the same manner as in Example 1, an A/B/C/D laminate was produced. It cannot be heat-sealed, it cannot be made into a bag, and it cannot be made into a container for secondary batteries. [Comparative Example 5] As the polypropylene film (D), an unaligned polypropylene film having a thickness of 40 μm, a breaking strength of 38 MPa, and a tensile elongation of Young's modulus of 630 MPa was used as the polypropylene film (D) (Toyobo Co., Ltd.) In the same manner as in Example i, except for "Pylenfilm-CT PlUl,", the A/B/C/D laminate was produced. The characteristics are shown in Table 1. [Comparative Example 6] In Example 1, As D, an unaligned polypropylene film having a thickness of 6 〇μηι of 47 MPa, a breaking elongation of 635%, and a Young's modulus of 630 MPa was used. Torayfan (registered trademark) n manufactured by Toray Film Processing Co., Ltd. 〇33〇1). In the same manner as in Example 1, an A/B/C/D laminate was produced. The characteristics are shown in the table! in. [Comparative Example 7] In Example 1, 'the polyester film (A) was not used. The A/B laminate was not formed. In the same manner as in Example 1, a B/c/D laminate was produced. The characteristics are shown in Table 1. -43-201222930 [Comparative Example 8] In Example 1, as D, an unaligned polypropylene film having a thickness of 40 μm of a breaking strength of 38 MPa, an elongation at break of 500%, and a Young's modulus of 585 MPa was used ( D) (Pylenfilm_CT Pll28, manufactured by Toyobo Co., Ltd.). In the same manner as in Example 1, an A/B/C/D laminate was produced. The characteristics are shown in Table 1. [Comparative Example 9] In Example 1, the A/B laminate was laminated with C' A and C, and the adhesive, the amount of the adhesive applied, and the aging treatment of the example ' were carried out to form a B/A/C laminate. material. Then, in the same manner as in Example 1, a B/A/C/D laminate was produced. The characteristics are shown in Table 1. [Comparative Example 10] A biaxially-oriented polyethylene terephthalate film (A) having a thickness of 12 μm, a breaking strength of 240 MPa, and an elongation at break of 181 % by a dry build-up method (A) "Lumirr〇r" (registered trademark) p6〇 manufactured by Co., Ltd.) and aluminum foil (c) having a thickness of 40 μm ("Vespa" 8021 manufactured by Light Aluminum Foil Co., Ltd.) 'Using Mitsui Chemical Polyurethane Co., Ltd. "Takelac A-910 (polyol-based main agent butyl akenate A_3 (isocyanate-based hardener), two-component type (丨〇〇 parts by weight / 丨〇 part by weight) of adhesive, made of A / C laminated material. Here The amount of the adhesive applied was 6 g/m 2 in terms of solid content on the A side, and after 45 ° and 80 hours of aging treatment after bonding to A/C, the thickness was 15 μm and the breaking strength was 1 〇 3 MPa by the dry laminate method. The unaligned nylon ruthenium film (b) having a breaking elongation of 398% ("Rayfan" (registered trademark) No. 1401 manufactured by Toray Film Processing Co., Ltd.) and -44 - 201222930 has a breaking strength of 35 MPa at a thickness of 70 μm. The elongation at break is 655°/., and the Young's modulus is 4 1 5 Μ P a. Acrylic film (D) ("Pylenfilm_CT P1 146" manufactured by Toyobo Co., Ltd.), "Takelac A-9 1 0 (polyol-based main agent)" manufactured by Mitsui Chemicals Polyamine Oxime Co., Ltd. /" Takenate A-3 (isocyanate-based hardener), 'two-component type (100 parts by weight/10 parts by weight) of adhesive, made of B/D laminate. The amount of adhesive applied here is 5g/g on the B side in terms of solid content. M2, after bonding at B/D, was aged at 40 ° C for 72 hours. The A/C laminate and the b/d laminate were extruded at a melt temperature of 140 ° C at a thickness of 10 μm. A modified polyolefin (manufactured by Mitsui Chemicals Co., Ltd., functionally graft-modified polypropylene "Adomer QE840") was laminated on the interlayer ' between C and B to form an a/C/B/D laminate. The system is shown in Table 1. [Comparative Example 1 1] The uncomplexed polypropylene having a breaking strength of 35 MPa and an elongation at break of 655 ° /. and a Young's modulus of 415 MPa by a dry laminate method Film (D) ("pyienfilm_CT P1146" manufactured by Toyobo Co., Ltd.) and thickness 15μπι, breaking strength i〇3Mpa, Unaligned nylon 6 film (B) with a crack elongation of j98 / ("Rayfan" (registered trademark) NO 1401, manufactured by Toray Film Processing Co., Ltd.), "Take" manufactured by Mitsui Chemicals Polyurethane Co., Ltd.丨μ A-9i〇 (polyol based agent) / Takenate A-3 (isocyanate-based hardener), two-liquid type (1〇〇 heavy injury / ίο reset part) adhesive, made d/b laminated material . Here, the adhesion Jk Brill was 5 g/m 2 on the B side in terms of solid content, and after the bonding, the lamp was aged for 40 C for 72 hours. -45- 201222930 By D-B laminated method, laminated D/B laminated material, 40μm thickness of Ming Foil (C) (Vespa "8021) made by Light Aluminum Foil Co., Ltd., Β and C 'Use Mitsui Chemical Polyamine A ''Takelac A-910 (polyol-based main agent), '/''Takenate A-3 (isocyanate-based curing agent)" two-liquid type (100 parts by weight / 10 parts by weight) adhesive The D/B/C laminate was prepared. The amount of the adhesive applied was 6 g/m2 on the B side in terms of solid content, and after bonding at D/B/C, the curing treatment was carried out at 45 ° C for 80 hours. Biaxially oriented polyethylene terephthalate film (A) with a thickness of 12 μm, a breaking strength of 240 MPa, and an elongation at break of 18% on a D/B/C laminate (Dongli Co., Ltd.) "Lumirror" (registered trademark) P60) is extruded at a temperature of 140 ° C at a thickness of ΙΟμπι, using a modified polyolefin (manufactured by Mitsui Chemicals, Inc., functionally graft-modified polypropylene "Adomer QE84" 〇") The interlayer between C and Α is laminated to form A/C/B/D laminate. The characteristics are shown in Table 1. [Comparative Example 12] In Example 30, a nylon 6 film (β) was used as a nylon 6 film (β) (a biaxial alignment film "Hardenfilm N.1100") manufactured by Toyobo Co., Ltd.). 3〇 Similarly, an A/B/C/D laminate was produced. The characteristics are shown in Table j. [Comparative Example 1 3] Except that in Example 30, modified polyolefin was not used, and Ube Industries was used instead. A high-density polyethylene made by the company, "υβΕpolyethylene L719' is melted, and the 'cover degree is other than 108C'. The a/B/C/D laminate is produced in the same manner. The characteristics are shown in Table 1. 201222930 [Comparative Example 14] In Example 30, the a/b/c laminate and the unaligned polypropylene film (D) ("Pylenfilm CT PI i46" manufactured by Toyobo Co., Ltd.) were laminated by a dry laminate method. C and D, "Takelac A_9l (polyol-based main agent)" / "Takenate A-3 (isocyanate-based hardener)" manufactured by Mitsui Chemicals Polyamine Co., Ltd., two-liquid type (1〇〇) A part by weight / 10 parts by weight of the adhesive was prepared as an A/B/C/D laminate. Here, the amount of the adhesive applied was 6 g/m 2 on the C side in terms of solid content, and was carried out after C/D bonding. The aging treatment was carried out at ° C for 80 hours, and the A/B/C/D laminate was produced in the same manner as in Example 3, and the characteristics are shown in Table 1. [Comparative Example 15] In Example 30, In the polypropylene film (D), an oriented polypropylene film having a thickness of 6 〇 μηη (Torayfan (registered trademark) 2500 制, manufactured by Toray Co., Ltd.) was used in the same manner as in Example 30. , made of A / B / C / D laminated materials. It cannot be heat-sealed and cannot be made into a bag. ‘The container for secondary batteries cannot be made. [Comparative Example 16] As the polypropylene film (D), an unoriented polypropylene having a thickness of 40 μm, a breaking strength of 38 MPa, an elongation at break of 51%, and a Young's modulus of 630 MPa was used as the polypropylene film (D). In the same manner as in Example 3, except for the film (Pylenfilm-CT P1111 manufactured by Toyobo Co., Ltd.), an A/B/C/D laminate was produced. The characteristics are shown in Table 1. [Comparative Example 17] In Example 30, as D, an unaligned polypropylene having a thickness of 6 〇μηι of 47 MPa, an elongation at break of 635%, and a Young's modulus of 63 〇Mpa -47 to 201222930 was used. Film (D) (Torayfan (registered trademark) NO 3301, manufactured by Toray Film Processing Co., Ltd.). Otherwise, in the same manner as in Example 30, an A / B / C / D laminate was produced. The characteristics are shown in Table 1 [Comparative Example 18] In Example 30, a polyester film was not used. In the same manner as in Example 30, a b/C/D laminate was produced in the same manner as in the a/B laminate. The characteristics are shown in Table 1. [Comparative Example 19] In Example 30, as D, an unaligned polypropylene film (D) having a thickness of 4 〇 μηη of 38 MPa, an elongation at break of 5%, and a Young's modulus of 585 MPa was used ( "Pyunfilm-CT P1128" manufactured by Toyobo Co., Ltd.). Otherwise, in the same manner as in Example 3, an A/B/C/D laminate was produced. The characteristics are shown in Table 2. [Comparative Example 20] In the case of the Example 30, the laminated A/B laminated material and the c and A were similarly subjected to the adhesive, the amount of the adhesive applied, and the aging treatment to form a B/A/C laminated material. . Then, in the same manner as in Example 30, a B/A/C/D laminate was produced. The characteristics are shown in the table ι. [Comparative Example 2 1 ] By a dry-laid method, a thick sound, an elongation at break of 118% of two: g -, a breaking strength of 27, and a 3 f-axis alignment of a polyethylene terephthalate film (A) (Dongli >Tactical Processing Co., Ltd. trademark) P375) and thickness 25μηι, (4)(10)1*" (2) Secretary system "Vespa" 8021), use:: Yangshen light 1 Lu pig shares limited company - well chemical polyamine Formate Co., Ltd. -48- 201222930 Takelace A-91〇 (Polyol Master), //Takenate A-3 (Isocyanate Hardener)'' Two Liquid Type (1 part by weight) "ο parts by weight" Adhesive 'made as A/C laminate. Here, the amount of the adhesive applied was 6 g/m 2 on the a side as a solid component, and 45 after the A/C bonding. (:, 80 hours of aging treatment. By the dry layer method, the unaligned nylon 6 film (B) having a thickness of 15 μπ1, a breaking strength of 1〇3 MPa, and a breaking elongation of A 3 98% (Dongli film force = industrial shares) Co., Ltd. "Rayfan" (registered trademark) N〇14〇1) and a thickness of 7〇μηι with a breaking strength of 35MPa, an elongation at break of 655%, and a Young's modulus of 415MPa (D) ( "Pylenfilm_CT P1 M6" manufactured by Toyobo Co., Ltd.), "Takelac A_91" (Polyol Master 1) / Takenate A-3 (Isocyanate-based curing agent) manufactured by Mitsui Chemicals Polyamine Oxalate Co., Ltd. , 'Two-component type (1 〇〇 part by weight/10 parts by weight) of adhesive, made of B/D laminate. Here, the amount of adhesive applied is 5g/m2 on the B side in terms of solid content, and is bonded to B/D. After the 'curing treatment at 40 ° C for 72 hours. The A/C laminate and the B/D laminate were extruded at i4 (the melting temperature of TC, at a thickness of ΙΟμηη, using modified polyolefin (Mitsui Chemicals) Co., Ltd., functional group graft modified polypropylene "Ad〇mer qE84〇,,) between C and B The interlayer was laminated to form an A/c/B/D laminate. The characteristics are shown in the table. [Comparative Example 2 2] The fracture strength of the thickness of 70 μm by the dry laminate method was 35 MPa, and the elongation at break was 655%, non-aligned polypropylene/film (D) with Young's modulus of 415 MPa (made by Toyobo Co., Ltd., py 1 enf丨丨(7)c τ -49- 201222930 卩1146'') and thickness of 111 An unaligned nylon 6 film (B) having a breaking strength of 1〇3^1^ and a breaking elongation of 398% ("Rayfan" (registered trademark) Ν〇ι4〇1, manufactured by Toray Film Processing Co., Ltd.), used "Take 丨ac A_91 〇 (polyol-based main agent)"' / "Takenate A-3 (isocyanate-based curing agent)", manufactured by Mitsui Chemicals Polyurethane Co., Ltd., two-liquid type (100 weights: 3: parts / 10 parts by weight of the adhesive was prepared as a D/b laminate. Here, the amount of the adhesive applied was 5 g/m 2 on the B side in terms of solid content, and 4 0 C, 72 hours after the D/B bonding. Curing treatment. Aluminum foil (C) with a thickness of 25 μm is laminated by D/B laminate (Vespa, manufactured by Light Aluminum Foil Co., Ltd.) 8021), Β and C' use "TakeUc A-910 (polyol-based main agent)" / "Takenate A_3 (isocyanate-based curing agent)" two-liquid type (1〇) manufactured by Mitsui Chemicals Polyamine Oxalate Co., Ltd. 〇 Parts by weight / 1 part by weight) Adhesive, made of D/B/c laminate. Here, the amount of the adhesive applied was 6 g/m 2 on the B side in terms of solid content, and after bonding at D/B/C, it was aged at 45 ° C for 80 hours, and applied to the D/B/C laminate. A biaxially-oriented polyethylene terephthalate film (A) having a thickness of 6.5 μm, a breaking strength of 275 MPa, and an elongation at break of 118% ("Lumirror" (registered trademark) P60, manufactured by Toray Industries, Inc.) The melting temperature of 140C was extruded at a thickness of ΙΟμιη, and a modified polyolefin (manufactured by Sanken Chemical Co., Ltd., "functional graft-modified polypropylene "Adomer QE840") was sandwiched between C and Α. The layer was laminated to form an A/c/B/D laminate. The characteristics are shown in Table 1 -50 to 201222930 [Comparative Example 23] In addition to the embodiment, in place of the biaxial alignment of polyethylene terephthalate Ester film (A) 'Used a thick aromatic 纟 4.5 _, a breaking strength of 6 〇〇 Mpa, and an elongation at break of 50%. The para-type aromatic polyamide film (Mictron, manufactured by Toray Industries, Inc.) In the same manner as in Example 30 except for the trademark ML), an A/B/C/D laminate was produced. The characteristics are shown in Table i. [Comparative Example 24] In addition to the two-oriented polyethylene terephthalate film (A) in Example 30, a two-axis having a thickness of 12 μm, a breaking strength of 23 5 MPa, and an elongation at break of 95% was used. An A/B was produced in the same manner as in Example 3 except that the thickness of the aluminum foil (C) was ΐ〇μπι, which was made of a polyethylene terephthalate film (Toyobo Esterfilm E51 (manufactured by Toyobo Co., Ltd.). /C/D laminate. The characteristics are shown in Table 1. [Comparative Example 2 5] In addition to Example 30, 'as a biaxially oriented polyethylene terephthalate film (Α), thickness 50 μm , a rupture strength of 6 〇 MPa, and an elongation at break of 3 6 5 %, a sleeve-aligned poly(p-diphenyl phthalate) film (T ef 1 e X ρ τ 7, manufactured by Teijin DuPont Film Co., Ltd. In the same manner as in Example 30, 'A / B / C / D laminated material was produced. The characteristics are shown in Table 1. [Comparative Example 2 6] In Example 51, 'as a nylon 6 film (b) ), a aligning nylon 6 film (a two-axis alignment film "Hardenfilm N1 100" manufactured by Toyobo Co., Ltd.) was used. In the same manner as in Example 51, an A/B/C/D laminate was produced. The characteristics are shown in Table i. -51 - 201222930 [Comparative Example 27] In Example 51, no modified polyolefin was used instead. A high-density polyethylene "UBE Polyethylene L719" manufactured by Ube Industries, Ltd. was used, and an A/B/C/D laminate was produced in the same manner except that the melting temperature was 10 ° C. The characteristics are shown in Table 1. [Comparative Example 28] In Example 51, a/B/C laminate and unaligned polypropylene film (D) (Pylenfilm-CT P1 146 manufactured by Toyobo Co., Ltd.) were laminated by a dry laminate method. , C and D, using "Takelac A-910 (Polyol Master) / Takenate A-3 (Isocyanate-Based Hardener)" manufactured by Mitsui Chemicals Polyurethane® Co., Ltd. /10 parts by weight of the adhesive, made of A/B/C/D laminated material. Here, the adhesive coating is 6 g/m2 on the C side in terms of solid content, and after C/D bonding, d, 80 is carried out. The aging treatment was carried out in the same manner as in Example 5 j, and the A/B/C/D laminate was produced. The characteristics are shown in Table 。. [Comparative Example 29] In Example 51 As the polypropylene film (D), an oriented polypropylene film having a thickness of 6 μm was used (a two-axis alignment polypropylene film "Torayfan" (registered trademark) 25" manufactured by Toray Industries, Inc.). Similarly, an A/B/C/D laminate was produced. It could not be heat-sealed and could not be made into a bag. [Comparative Example 30] Except for the implementation of your "1 towel, as the polypropylene film (d), an unoriented polypropylene having a thickness of 40, a breaking strength of 38 MPa, an elongation at break of other %, and a Young's modulus of 630 MPa was used. A film of A/B/C/D was produced in the same manner as in Example 5 except that the film (Pylenfilm-CT PI 1 1 1) manufactured by Toyo Seiki Co., Ltd. was manufactured by Toyo Co., Ltd.. The characteristics are shown in Table 1. [Comparative Example 3 1] In Example 51, 'as D, an unaligned polypropylene film (D) having a thickness of 60 μηι having a breaking strength of 47 MPa, an elongation at break of 63 5%, and a Young's modulus of 630 MPa was used ( "Torayfan" (registered trademark) NO 3301 manufactured by Toray Film Processing Co., Ltd.). Otherwise, in the same manner as in Example 5-1, an A/B/C/D laminate was produced. The characteristics are shown in Table 1. 〇 [t匕 Comparative Example 3 2 ] In Example 51, no polyester film was used. A/B laminate was not produced. In the same manner as in Example 51, a B/C/D laminate was produced. The characteristics are shown in Table 1. [Comparative Example 3 3] In Example 51, as a crucible, an unaligned polypropylene crucible having a thickness of 40 μm and a breaking strength of 38 MPa, an elongation at break of 5 Å/q, and a Young's modulus of 585 MPa was used. (D) (Pylenfilm-CTP1128, manufactured by Toyobo Co., Ltd.). In the same manner as in Example ^, an A/B/C/D laminate was produced. The characteristics are shown in Table 1. [Comparative Example 3 4] In Example 51, the A/B laminate was laminated with C, A and C, and the adhesive, the amount of the adhesive applied, and the aging treatment of Example 51 were prepared in the same manner as in the case of B/A/ C laminated material. Then, in the same manner as in Example #1, a B/A/C/D laminate was produced. The characteristics are shown in the table. [Comparative Example 3 5 ] -53- 201222930 The two-axis alignment polyethylene terephthalate (Μ 由 由 由 又 又 又 厘 厘 厘 又 又 又 又 又 又 又 又 又 又 又 又 又 又 又 又 又 又 又 又 又 又 又 又(Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te "Takelac A-910 (polyol-based main agent), /" Takenate A 3 (cyanic acid I-based curing agent), 'two-liquid type (100 parts by weight / 1 part by weight) adhered by Ester Co., Ltd. Agent, made A / C layer #. Here, the amount of the coating agent applied was 6 g/m2 in terms of solid content on the eight sides of the crucible, and after the A/C bonding, the curing treatment was carried out for 45 t and 8 hours. An unaligned nylon 6 film (B) having a thickness of 15 μm and a breaking strength of ι〇3Μρ& elongation at break of 398% by dry-laid method ("Rayfan" (registered trademark) N manufactured by Toray Film Processing Co., Ltd. "Non-aligned polypropylene film (D) (Pylenfilm_CT P1 146, manufactured by Toyobo Co., Ltd.) having a breaking strength of 35 MPa, a breaking elongation of 655%, and a Young's modulus of 415 MPa. "Takelac A_91" (Polyol based agent) / Takenate A-3 (isocyanate-based curing agent) manufactured by Mitsui Chemicals Polyurethane Co., Ltd., two-component type (1 part by weight / 10 parts by weight) The adhesive is used to form a B/D laminate. Here, the amount of the adhesive applied is 5 g/m 2 on the B side in terms of solid content, and after bonding at B/D, the curing treatment is carried out at 40 ° C for 72 hours. The A/C laminate and the β/D laminate were extruded at a melting temperature of 14 〇t at a thickness of 1 Ομηι, using a modified polyolefin (manufactured by Mitsui Chemicals, Inc., functional group graft modified poly Propylene "Adomer QE840") is laminated in the interlayer between C and B, A/C/B/D laminate. The characteristics are shown in Table 1. -54 - 201222930 [Comparative Example 36] The fracture strength of the 厘 ΐ 70 thickness 70 μπι is 35 Μρ & Unaligned aggregation of 655% and Young's modulus of 415

丙稀薄膜⑼(東洋纺績月史份有限公司製“pyienfUm_cT P1146 )與厚度15μηι、斷裂強度為mMpa、斷裂伸長度 為398%的無配向尼龍6薄膜(B)(東麗薄膜加工股份^ 公司製「Rayfan」(註冊商標)N〇 14〇1),使用三井化學 聚胺曱酸酿股份有限公司製的”Take丨ae A_9 1()(多元醇系 主劑),,/“Takenate A_3(異氰酸酿系硬化劑),,二液型(1〇〇 重量份m重量份)黏著劑,料㈣積層材。此處,點 著劑塗布量以固體成分計在B側為5〆,於購貼合 後,進行4〇°C、72小時的熟化處理。 藉由乾積層法,疊合D/B積層材、厚度25μηι的鋁 箔(C)(住輕鋁箔股份有限公司製“Vespa” 8021、Β與C, 使用三井化學聚脸甲缺 卞月甲酉文酉曰股份有限公司製的“Takelac A-9叫多元醇系主劑…(異…旨系硬化 片J) 一液|(1〇〇重置份/1〇重量份)黏著劑,作成 積層材。此處點菩逾丨务士 θ " 1 考Μ I布I係在Β側以固體成分計為 6g/m2,於 D/B/c 目J;人祕 ^ 貼口後’進行45T:、80小時的熟化處 理。 於D/B/C積層材上’將厚度25μιη、冑裂強度為 a斷氣伸長度為2 1 5 °/。的二軸配向聚對苯二甲酸 西曰'專膜(A)(帝人杜邦薄膜股份有限公司製“Teflex” FT3)在140 C的溶融溫度’以i〇]Lim的厚度壓出,使用改 -55- 201222930 性聚烯烴(三井化學股份有限公司製,官能基接枝改性 聚丙烯“Adomer QE840”)於C與A之間的夾層,進行積 層,作成A/C/B/D積層材。特性係顯示於表1中。 [比較例37] 除了於實施例5 1中,代替二軸配向聚對苯二曱酸乙 二酯薄膜(A),使用厚度50μιη、斷裂強度為60MPa、斷 裂伸長度為3 6 5 %的二軸配向聚對苯二曱酸乙二酯薄膜( 帝人杜邦薄膜股份有限公司製“Teflex” FT7)以外,與實 施例5 1同樣地,作成A/B/C/D積層材。特性係顯示於表 1中。 [比較例3 8 ] 除了於實施例5 1中,作為二軸配向聚對笨二曱酸乙 二酯薄膜(A),使用厚度Ι6μιη、斷裂強度為177MPa、斷 裂伸長度為1 60%的二軸配向聚對苯二曱酸乙二酯薄膜( 東麗薄膜加工股份有限公司製「Lumirror」(註冊商標 )F865)以外,與實施例51同樣地,作成A/B/C/D積層材 。特性係顯示於表1中。 [比較例3 9 ] 除了於實施例5 1中,作為二軸配向聚對苯二曱酸乙 二酯薄膜(A),使用厚度38μιη、斷裂強度為260MPa、斷 裂伸長度為1 6 8 %的二軸配向聚對苯二曱酸乙二酯薄膜( 東麗薄膜加工股份有限公司製「Lumirror」(註冊商標 )F99)以外,與實施例51同樣地,作成A/B/C/D積層材 。特性係顯示於表1中。 -56- 201222930 [比較例4 0 ] 除了於實施例5 1,作為二轴配向聚對苯二曱酸乙二 酯薄膜(Α),使用厚度38 μιη、斷裂強度為265MPa、斷裂 伸長度為1 70%的二軸配向聚對苯二甲酸乙二酯薄膜(東 麗股份有限公司製「Lumirror」(註冊商標)ΤΙ 1)以外,與 實施例5 1同樣地,作成A/B/C/D積層材。特性係顯示於 表1中。 -57- 201222930 【1丨1<】 積層材 積層順序 ^VB/C/改性 PO/D A/B/C/改性 PO/D A/B/C/改性 PO/D [VB/C/改性 PO/D ^VB/C/改性 PO/D A/B/C/改性 PO/D ^VB/C/改性 PO/D A/B/C/改性 PO/D A/B/C/改性 PO/D A/B/C/改性 PO/D A/B/C/改性 PO/D |A/B/C/改性 PO/D 1 A/B/C/改性 PO/D ^VB/C/改性 PO/D 1 ^VB/C/改性 PO/D | !A/B/C/改性 PO/D 1 ^/B/C/改性 PO/D >VB/C/改性 PO/D A/B/C/改性 PO/D 1 A/B/C/改性 PO/D A/B/C/改性 PO/D A/B/C/改性 PO/D A/B/C/改性 PO/D A/B/C/改性 PO/D 耐衝擊性 财振動性-3 耐振動性-2 财振動性-1 〇 〇 〇 〇 〇 〇〜△ < 〇 ο ι 〇 〇 〇 〇 < < < 〇 <1 <1 <1 成形性 |mm oo o 00 KT) VO ON o Q\ ιη oo 00 oo oo 00 oo 卜 卜 卜 oo V) SO 卜 聚两烯薄膜(D) 楊氏模數 [MPa 寸 ίΛ ir> 寸 m 〇 OO 500 1 500 1 500 rf m U-J 寸 to 寸 寸 1〇 U-) 寸 vn in iT) 斷裂伸長度 «/") Ό <n v〇 v〇 iTj i〇 Ό v〇 u-) V〇 655 570 730 730 480 |655 | in yr\ Ό ^55_1 Ό SO U-I 655 in \r> 655 ID l〇 VO ^Ti 'sn ^TJ \n vr> 斷裂強度 |MPa in r^) m P〇 m r〇 tr» m A o m «Ο U-J r^) m r<) ΙΛ> iT> 配向 瑞 瑞 磡 端 瑞 尼龍6薄膜(B) 斷裂伸長度 00 ON f<*| 398 398 398 398 398 j 398 00 o 〇〇 O'· 398 398 ^98 | b98 398 OO ON m 398 | 398 398 398 | 398 oo 〇\ 00 On 398 398 斷裂強度 |MPa S s s s s s s s S s s s S s S s s s s s s s s s 配尚 碳 瑞 #: 难 瑞 难 裸 墉 璀 碟 璀 m 瑞 薄膜(A) 斷裂伸長度 OO 00 CN § o § CO oo oo 00 oo oo oo oo 00 CO oo oo oo 00 o V-) CN ^Ti 斷裂強度 |MPa 240 1 225 216 | § _1 o ο rS ο N_I o o rs o JN O 240 I o rs ο 240 | 〇 o <n (N w*i oo S 配向 二轴 二軸 二軸 二袖 二轴 二轴 Ί Ί 二轴 二轴 處 Ί 器 二軸 器 Ί 二軸 器 Ί 器 Ί 二轴1 Ί 器 Ί 二轴 器 Ί Ί 素材 PET PLA PET PET PLA PET PETi PET ΡΕΤ| PETl PFT PET PET PET PET PET PET PET pet! PET PEN PET PET PET 實施例1 實施例2 實施例3 實施例4 實施例5 實施例6 實施例7 丨實施例8 1 實施例9 1 實施例10: 丨實施例π 1 丨實施例丨21 |實施例n| 實施例14 丨實施例15 | |實施例丨6| |實施例17| 1實施例18| |實施例19| 1實施例2〇| 實施例21 |實施例22 I |實施例23 1 |實施例24 I 盟 Μ0结fr--r 池鉍:z3d ISIro^B-M^feie :HHd ,οος — ¾¾鉍:od 铛祐鉍:νΊο- 201222930 【<N—I <】 積層材 1積層順序 A/B/C/改性 PO/D A/B/C/改性 PO/D ^V/B/C/改性 PO/D A/B/C/改性 PO/D A/B/C/改性 PO/D A/B/C/改性 PO/D |A/B/C/改性 PO/D 1 A/B/C/改性 PO/D ^V/B/C/改性 PO/D A/B/C/改性 PO/D A/B/C/改性 PO/D h/B/C/改性 PO/D I lA/B/C/改性 PO/D A/B/C/改性 PO/D A/B/C/改性 PO/D A/B/C/改性 PO/D A/B/C/改性 PO/D A/B/C/改性 PO/D A/B/C/改性 PO/D A/B/C/改性 PO/D A/B/C/改性 PO/D A/B/C/改性 PO/D | A/B/C/改性 PO/D A/B/C/改性 PO/D 耐衝擊性 1耐振動性-3 耐振動性-2 〇 〇 〇 〇 〇 〇 〇 〇 o o <1 <1 < o 〇 〇〜△ | <1 o 对振動性-1 〇 < 〇 0 < 成形性 |mm OO o iT) ir> o 聚丙烯薄膜(D) 楊氏模數 |MPa 415 415 1 |415_1 5 Ki5_! 415 o OO m o O o s 415 415 415 415 415 415 415 | 415 415 斷裂伸長度 in 655 655 655 655 655 丨655 ^55_I 655 | 〇 730 730 k80 655 655 655 655 655 655 655 655 | 655 in <n 斷裂強度 |MPa r·) i〇 r·) yrt r^) IT» r<) l/·) ro A o r^) i〇 ITJ r<-| w-i r<·) l〇 r<*) 配向 难 难 难 碟 磡 碟 瑞 瑞 磯 碳 墉 磲 碳 难 墀 瑞 墀 磲 4i 尼龍6薄膜(B) 斷裂伸長度 OO 〇\ OO ON m OO Q\ r〇 OO CN 398 OO Os OO ON ΓΛ OO 〇 γ<Ί OO ON ΓΛ 398 OO 〇s r·) OO Os ΓΛ OO Os r*·) OO Os r^) OO On OO 〇s 398 OO as r*·) OO On r") OO Os OO ON Γη 398 | OO CN 398 斷裂強度 |MPa S S S s s S S S s s S s S S s s s S S s s s S s 配向 薄膜(A) 斷裂伸長度 OO OO OO 365 CO OO OO VO o OO U-) CN g OO OO OO OO OO OO OO OO OO OO OO OO OO OO 斷裂強度 |MPa o 240 240 s o 275 〇 f*·) OO 480 | m_I JO m_ ¢75 JO rs JO 275 275 275 275 275 275 | i〇 JO |配向 二軸 二轴 二軸 龙 Ί 二轴 二轴 t Ί t M Ί 二軸 t 二轴 二軸 t Ί 器 Ί ί ί 二抽 眾 Ί 器 Ί 器 M 器 Ί 素材 PET PET PET PET PET PET PET PEN! petI < cu PET PET PET PET PET PET PET PET PET PET PET PET PET PET 實施例25 實施例26 實施例27 實施例28 實施例29 實施例30, |實施例31 , 匳施例32 | 實施例33 1 實施例34 S |實施例351 「實施例36 1 「實施例37 1 施例38 | 實施例39 |實施例40 | |實施例411 |實施例42 | 實施例43 實施例44 |實施例45 i |實施例46 I |實施例47 I |實施例48 | ISMO^fr-M 掩鉍:z3d 遛-^0湓»-4}4寂鉍:13d -6ς- ¾¾¾ :〇dwsssi^^ikf^isiva. ^¾½ : v_ld 201222930 【e-I ΐ 積層材 |積層順序 ^V/B/C/改性 PO/D A/B/C/改性 P0/D ^VB/C/改性 PO/D A/B/C/改性 PO/D |A/B/C/改性 PO/D I A/B/C/改性 PO/D ^VB/C/改性 PO/D A/B/C/改性 PO/D [A/B/C/改性 PO/D 1 ^VB/C/改性 PO/D A/B/C/改性 PO/D A/B/C/改性 PO/D ^/B/C/改性 PO/D A/B/C/改性 PO/D |a/B/C/改性 PO/D ^i/B/C/改性 PO/D A/B/C/改性 PO/D A/B/C/改性 PO/D A/B/C/改性 PO/D | A/B/C/改性 PO/D A/B/C/改性 PO/D A/B/C/改性 PO/D A/B/C/改性 PO/D | A/B/C/改性 PO/D 耐衝擊性 〇 〇 〇 〇 〇 〇 〇 〇 < < < < o 〇〜△ 〇〜△ o 〇〜△ 〇 o o o 耐振動性-3 〇 〇 〇 〇 〇 〇 〇 〇 < < o Ό〜Λ 〇〜△ o 〇〜△ O o o o 耐振動性-2 |〇〜Δ 〇 耐振動性-1 成形性 |mm 聚丙烯薄膜(D) 楊氏模數 |MPa 寸 ir> 寸 W-J 寸 380 500 500 ^00 ^15 415 ; U-l 415 ^15 415 U-) 415 415 | 415 415 415 | 415 斷裂伸長度 |655 m \〇 li-l in wo Ό in v〇 o MX 730 730 |480 | •ο in ^55_I w-i VJ? »·〇 ir> \〇 ΙΛ) Ό Ό »r> to V〇 ITi IT5 \〇 so m 655 iTi vn IT) ΙΛ Ό in in \n in \r> 斷裂強度 [MPa ΙΛ Γ〇 in r^) r<l i〇 r^l Pl o tr> r·) r^) in r·) yn r^) r^i r〇 配向 尼龍6薄膜(B) 斷裂伸長度 |398 398 OO Os r^) 398 398 OO Q\ 398 398 β98 i 00 〇\ ΡΛ 398 398 00 〇s 398 398 00 On OO ON 398 398 | 398 398 398 398 | oo Os 斷裂強度 |MPa S s S s s S s 00 o s s s s S s s S S s s s s s s S 配向 薄膜(A) 斷裂伸長度 00 oo § o o ?] in 215 |2I5 cs 215 ?; V-) ID fq i〇 n 215 | 215 215 〇s OO 00 <N OO 斷裂強度 [MPa (275 uo V〇 ON in Ό ό v〇 Ό 〇 SO Ό 2 ·〇 Ό IT) VO in v〇 s s 5 250 | 232 配向 M 器 Ί M 器 Ί 器 Ί 二軸 二軸 Ί 二轴 港 Ί 器 Ί t Ί 器 Ί 器 二軸 t Ί t M Ί 器 Ί fl fi 素材 ΡΕΤ PET PET PET PET PET PET PET丨 PET PET PET PET |PET ;PET PET PET PET PET PET PET PET PET PET pet| 1實施例49 實施例50 實施例51 實施例52 實施例53 實施例54 實施例55 實施例56! 丨實施例57 | 丨實施例58 1 |實施例591 |實施例60 I |實施例6】1 實施例62 |實施例63 1 丨實施例64 1 丨實施例651 實施例66 |實施例67 | |實施例68 | |實施例69 I 實施例70 |實施例71 I 1實施例72 1 -09- ls-r(o*«(s®-M 浓鉍:z3d ISMlo^B-Mi4i554: 13d 201222930 【寸'<】 積層材 |積層順序 | A/B/C/改性 PO/D Ia/b/c/pe/d I A/B/C/D A/B/C/改性 PO/D A/B/C/改性 PO/D A/B/C/改性 PO/D B/C/D [A/B/C/改性 PO/D I B/A/C 改性 PO/D A/C/B/D ^改性 PO/C/B/D | ^VB/C/改性 PO/D A/B/C/PE/D A/B/C/D A/B/C/改性 PO/D A/B/C/改性 PO/D A/B/C/改性 PO/D B/C/D A/B/C/改性 PO/D | B/A/C 改性 PO/D |耐衝擊性: 1耐振動性-3 |耐振動性-2 XX XX XX 1 X X XX XX | XX 耐振動性-1 XX X XX 1 X χ XX X X XX j XX X X @形性| [mm 1 oo 00 1 卜 卜 ON 卜 <?s 〇\ 〇s 聚丙烯薄膜(D) 氏模數 |MPa 415 W-ϊ 415 3012 |630 630 415 Vi oo »/*> 415 | 415 ^r, 415 415 415 β012 ο m \〇 630 W-l <r> oo in 415 1斷裂伸長度 655 in 655 (N 〇\ |510 ν〇 655 500 «·〇 ΙΛ SO U*i <ς> J655 655 655 (N ON 510 w-) u-i W-) vj-> 500 | in 1斷裂強度 [MPa ρη in OO oo 00 卜 »r> 00 U-) r〇 r^) »r> r^) 00 00 oo 卜 00 f^) r<) 配向; 难 墀 碟 器 Ί 碟 难 m 瑞 碟 m 难 碳 5 »1 碳 碳 墉 雄 尼龍6薄膜(B) I斷裂伸長度I oo ON οη 00 Os CO oo On r1) 00 ON n OO 〇\ oo On oo oo as r<) oo ON Γ*") oo 〇\ ΡΛ υ-1 oo oo Os oo 〇\ r*1) 398 oo ON oo ON OO 〇\ 398 | oo OS |斷裂強度| |MPa 1 00 S s S s s s S S s s 穿 rs S S s s S S s s 配向 慕 礫 磡 瑞 墀 璀 埦 难 瑞 磔 Ί 埦 璀 媸 墉 墀 难 媸 薄膜(A) 1斷裂伸長度 00 oo 00 OO 00 00 00 oo oo oo 00 OO 00 00 OO OO 1 00 00 1斷裂強度 |MPa 240 240 240 240 [240 o 1 _I o ^4〇_I o 卜 (N 275 JQ 275 jn CN JO rs I JO (N 275 配向 二轴 器 Ί 二轴 二轴 Μ 器 Ί ! Ί 器 Ί \Ξ^\ 者 Ί 课 Ί 二軸 t Μ 器 Ί 二軸 器 Ί 1 t Ί ί 素材 PET PET PET PET, PET| PET 1 pet] PET PET |PET PET PET PET PET] PET PET 1 PET PET 比較例1 比較例2 比較例3 比較例4 1比較例5 1 |比較例6 I 丨比較例7 1 ft匕較例8 1 [t匕較例9 | f比較例io| [fc匕較例11 ] 比較例12 「比較例13 | 比較例14 [比較例15 1 比較例16 |比較例17| 比較例18 |比較例19| 比較例20 sMo^B--r 摊鉍:z3d IS-r-o^B-M^^si: lUJd 敦$鉍:〇d 绉饍鉍璣咖米w^is: vcu 留^¾ : vlcu 201222930 【S_I<】 積層材 1積層順序 A/C/改性 PO/B/D A/改性 PO/C/B/D A/B/C//改性 PO/D A/B/C/改性 P0/D ^VB/C/改性 P0/D A/B/C/改性 P0/D A/B/C/PE/D |a/b/c/d I ^/B/C/改性 P0/D A/B/C/改性 P0/D ^VB/0/改性 P0/D 1 !b/c/d A/B/C/改性 P0/D B/A/C/改性 P0/D A/C/改性 PO/B/D A/改,f± P0/C/B/D A/B/C/改性 P0/D A/B/C/改性 P0/D A/B/C/改性 P0/D | A/B/C/改性 P0/D 耐衝擊性 XX XX NX ! X χ XX kx XX XX XX X X X X 耐振動性-3 XX XX ^<x 1 X χ XX Xx XX p<X Xx X X X y 耐振動性-2 XX XX X X |xx 对振動性-1 成形性1 聚丙烯薄膜(D) 楊氏模數 tMPa 415 415 5 415 415 415 ^15_I 3012 沄 |63〇_I 00 1/) ^15 ¢15_1 ^15 <n «n 415 斷裂伸長度· in Ό ITi Ό 655 «·〇 in VO IT) so 655 ^55_I <N o IT) <^ί iT) Ό o 655 »·〇 κη Ό Ό so Ό ir> »/*» 斷裂強度 |MPa ΙΛ υΊ r<> U-) r*") ID oo 00 oo r*~i 卜 00 in f^) «/> r<) ir> ir> f^| «Ο m |配向 璀 m 璀 5 M 碳 瑞 难 碟 难 尼龍6薄膜(B) 斷裂伸長度 00 σ\ 〇〇 On 〇〇 〇s 398 |398 u-» 00 398 |398 | oo 〇\ OO σ\ Γη OO σν Γ<Ί 00 ON ^98 398 β98 398 oo ON r*) 398 OO <7\ r^) 398 斷裂強度 (MPa s S s s s CO s s S S S s s s s s s s S s P己向 碳 碡 二軸 碳 难 碳 墀 磲 碳 墀 埤 碟 碟 碳 薄膜(A> 斷裂伸長度 00 00 l〇 ON [365 trj 215 ; IT) n IT) 刁 Μ rs 1 215 ID Π «/) Ό s〇 m s oo Ό o 斷裂強度 |MPa 275 275 o \〇 235 g Ό so in Ό v〇 1 »ri m vO tr> VO S r- 〇 Ό Ό 配向 二轴 器 M ff 二軸 器 Ί 二軸| \Ξ^\ 器 Ί 二軸 器 Ί 1 二轴 器 Ί 二軸 器 Ί z Ί i M '! 器 Ί 素材_ PET PET < PETI PET PETl PET PET PET PET ;PET 1 PET PET PET PET PET PET PET pet| 比較例21 比較例22 比較例23 比較例24 |比較例25 比較例26! 丨比較例271 |比較例28 ] |比較例29 I 比較例30 丨比較例31 1 |比較例32 1 |比較例33 | 比較例34 |比較例35 1 比較例36 比較例37 比較例38 |比較例39| 比較例40 SMO^B-M 滹鉍:z3d isMo?sB-Mi4si54: IddAcrylic film (9) ("pyienfUm_cT P1146" manufactured by Toyobo Masashi Co., Ltd.) and unaligned nylon 6 film (B) with a thickness of 15μηι, a breaking strength of mMpa, and an elongation at break of 398% (Dongli Film Processing Co., Ltd. "Rayfan" (registered trademark) N〇14〇1), using "Take丨ae A_9 1() (polyol-based agent) manufactured by Mitsui Chemicals Polyamine Tannin Co., Ltd., /"Takenate A_3 ( Isocyanic hardening agent), two-component type (1 part by weight by weight by weight) of adhesive, material (four) laminated material. Here, the amount of the coating agent applied was 5 Å on the B side in terms of solid content, and after aging, the aging treatment was carried out at 4 ° C for 72 hours. By dry layering method, laminated D/B laminated material, aluminum foil (C) with thickness of 25μηι (Vespa) 8021, Β and C made by Light Aluminum Foil Co., Ltd., using Mitsui Chemicals "Takelac A-9, a company made by the company, is called a polyol-based main agent... (Immediately, it is a hardened sheet J). One liquid | (1 〇〇 replacement part / 1 part by weight) of an adhesive is made into a laminate. 1 菩 丨 丨 θ θ 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 Hours of aging treatment. On the D/B/C laminate, the thickness of 25 μm, the splitting strength is a gas-breaking elongation of 2 15 ° /. The biaxial alignment of the polyterpene terephthalate film (A (Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te Te The graft modified polypropylene "Adomer QE840") was laminated in the interlayer between C and A to form an A/C/B/D laminate. The characteristics are shown in Table 1. Example 37] In addition to the biaxially oriented polyethylene terephthalate film (A), a biaxial alignment having a thickness of 50 μm, a breaking strength of 60 MPa, and an elongation at break of 365 % was used instead of the biaxially oriented polyethylene terephthalate film (A). A/B/C/D laminate was produced in the same manner as in Example 51 except that a polyethylene terephthalate film ("Teflex" FT7 manufactured by Teijin DuPont Film Co., Ltd.) was used. The characteristics are shown in Table 1. [Comparative Example 3 8] In addition to Example 51, as a biaxially aligned poly(p-ethylene phthalate film (A), a thickness of Ι6 μm, a breaking strength of 177 MPa, and an elongation at break of 160% were used. A/B/C/D laminate was produced in the same manner as in Example 51 except that a biaxially-oriented polyethylene terephthalate film ("Lumirror" (registered trademark) F865) manufactured by Toray Film Processing Co., Ltd. was used. The properties are shown in Table 1. [Comparative Example 3 9] In addition to Example 51, as a biaxially-oriented polyethylene terephthalate film (A), a thickness of 38 μm and a breaking strength of 260 MPa were used. Biaxially oriented polyethylene terephthalate film with elongation at break of 168% (Toray film) A/B/C/D laminates were produced in the same manner as in Example 51 except for "Lumirror" (registered trademark) F99 manufactured by Seiko Co., Ltd. The characteristics are shown in Table 1. -56 - 201222930 [Comparative Example 4 0 ] In addition to Example 5 1, as a biaxially oriented polyethylene terephthalate film (Α), a biaxial alignment pair with a thickness of 38 μm, a breaking strength of 265 MPa, and an elongation at break of 1 70% was used. An A/B/C/D laminate was produced in the same manner as in Example 51 except that the ethylene phthalate film ("Lumirror" (registered trademark) ΤΙ 1 manufactured by Toray Industries, Inc.) was used. The characteristics are shown in Table 1. -57- 201222930 [1丨1<] Laminated layer stacking order ^VB/C/modified PO/DA/B/C/modified PO/DA/B/C/modified PO/D [VB/C/Change PO/D ^VB/C/modified PO/DA/B/C/modified PO/D ^VB/C/modified PO/DA/B/C/modified PO/DA/B/C/modified PO/DA/B/C/modified PO/DA/B/C/modified PO/D | A/B/C/modified PO/D 1 A/B/C/modified PO/D ^VB /C/modified PO/D 1 ^VB/C/modified PO/D | !A/B/C/modified PO/D 1 ^/B/C/modified PO/D > VB/C/ Modified PO/DA/B/C/modified PO/D 1 A/B/C/modified PO/DA/B/C/modified PO/DA/B/C/modified PO/DA/B/ C/modified PO/DA/B/C/modified PO/D impact resistance vibrancy-3 vibration resistance-2 vibrancy-1 〇〇〇〇〇〇~△ < 〇ο ι 〇〇 〇〇<<<<〇<1<1<1 Formability|mm oo o 00 KT) VO ON o Q\ ιη oo 00 oo oo 00 oo Bu Bu oo V) SO Bupoly Film (D) Young's modulus [MPa inch Λ ir 寸 500 500 500 500 500 500 500 500 500 500 500 500 500 500 500 500 500 500 500 500 500 500 500 500 500 500 500 500 500 500 - - - - - - - - - - - - - - - - - - - - - l l l l l l l l t;nv〇v〇iTj i〇Ό v〇u-) V〇655 570 730 730 480 |655 | in yr\ Ό ^55_1 Ό SO UI 655 in \r> 655 ID l〇VO ^Ti 'sn ^TJ \n vr> breaking strength|MPa in r^) m P〇mr〇tr» m A om «Ο UJ r^) m r<) ΙΛ>iT> Alignment of Ruirui Duan Rui nylon 6 film (B) elongation at break Degree 00 ON f<*| 398 398 398 398 398 j 398 00 o 〇〇O'· 398 398 ^98 | b98 398 OO ON m 398 | 398 398 398 | 398 oo 〇\ 00 On 398 398 Breaking strength | MPa S Ssssssss S sss S s S sssssssss ssssssssss ssssssssss s s s s o V-) CN ^Ti Fracture Strength|MPa 240 1 225 216 | § _1 o ο rS ο N_I oo rs o JN O 240 I o rs ο 240 | 〇o <n (N w*i oo S Alignment Two Axis Two-axis two-axis two-sleeve two-axis two-axis Ί Ί Two-axis two-axis Ί two-axis Ί two-axis Ί Ί two-axis 1 Ί Ί Ί Ί 素材 material PET PLA PET PET PLA PET PETi PET ΡΕΤ|PETl PFT PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET Example 10: 丨Example π 1 丨Example 丨21 |Example n| Example 14 丨Example 15 | |Example 丨6| |Example 17|1 Example 18| |Example 19|1 Implementation Example 2 | Example 21 | Example 22 I | Example 23 1 | Example 24 I Allied 0 knot fr--r Pool: z3d ISIro^BM^feie: HHd, οος — 3⁄43⁄4铋: od 铛佑铋:νΊο- 201222930 [<N-I <] Laminated material 1 laminated sequence A/B/C/modified PO/DA/B/C/modified PO/D ^V/B/C/modified PO/ DA/B/C/modified PO/DA/B/C/modified PO/DA/B/C/modified PO/D | A/B/C/modified PO/D 1 A/B/C/ Modified PO/D ^V/B/C/modified PO/DA/B/C/modified PO/DA/B/C/modified PO/D h/B/C/modified PO/DI lA/ B/C/modified PO/DA/B/C/modified PO/DA/B/C/modified PO/DA/B/C/modified PO/DA/B/C/modified PO/DA/ B/C/modified PO/DA/B/C/modified PO/DA/B/C/modified PO/DA/B/C/modified PO/DA/B/C/modified PO/D | A/B/C/modified PO/DA/B/C/modified PO /D Impact resistance 1 Vibration resistance-3 Vibration resistance-2 〇〇〇〇〇〇〇〇oo <1 <1 < o 〇〇~△ | <1 o For vibration -1 〇&lt ;〇0 <formability|mm OO o iT) ir> o polypropylene film (D) Young's modulus|MPa 415 415 1 |415_1 5 Ki5_! 415 o OO mo O os 415 415 415 415 415 415 415 | 415 415 Elongation at break in 655 655 655 655 655 丨655 ^55_I 655 | 〇730 730 k80 655 655 655 655 655 655 655 655 | 655 in <n breaking strength|MPa r·) i〇r·) yrt r^ ) IT» r<) l/·) ro A or^) i〇ITJ r<-| wi r<·) l〇r<*) Alignment difficult 磡 磡 瑞 瑞 Ruiji carbon 墉磲 carbon difficult 墀墀磲4i Nylon 6 film (B) Elongation at break OO 〇\ OO ON m OO Q\ r〇OO CN 398 OO Os OO ON ΓΛ OO 〇γ<Ί OO ON ΓΛ 398 OO 〇sr·) OO Os ΓΛ OO Os r*·) OO Os r^) OO On OO 〇s 398 OO as r*·) OO On r") OO Os OO ON Γη 398 | OO CN 398 Breaking strength|MPa SSS ss SSS ss S s SS sss SS sss S s Alignment film (A) Elongation at break OO OO OO 365 CO OO OO VO o OO U-) CN g OO OO OO OO OO OO OO OO OO OO OO OO OO OO breaking strength|MPa o 240 240 so 275 〇f*·) OO 480 | m_I JO m_ ¢75 JO rs JO 275 275 275 275 275 275 | i〇JO | Alignment two-axis two-axis two-axis dragon Ί two-axis Two-axis t Ί t M Ί Two-axis t two-axis two-axis t Ί Ί ί ί Two-pumper Ί M M 素材 material PET PET PET PET PET PET PET PEN! petI < cu PET PET PET PET PET PET PET PET PET PET PET PET PET PET Example 25 Example 26 Example 27 Example 28 Example 29 Example 30, | Example 31, Example 32 | Example 33 1 Example 34 S | Example 351 Example 36 1 "Example 37 1 Example 38 | Example 39 | Example 40 | | Example 411 | Example 42 | Example 43 Example 44 | Example 45 i | Example 46 I | Example 47 I | Example 48 | ISMO^fr-M Cover: z3d 遛-^0湓»-4}4 Lonely: 13d -6ς- 3⁄43⁄43⁄4 :〇dwsssi^^ikf^isiva. ^3⁄4 1⁄2 : v_ld 201222930 [eI ΐ laminate] stacking order ^V/B/C/modified PO/DA/B/C/modified P0/D ^VB/C/modified PO/DA/B/C/change PO/D |A/B/C/modified PO/DIA/B/C/modified PO/D ^VB/C/modified PO/DA/B/C/modified PO/D [A/B /C/modified PO/D 1 ^VB/C/modified PO/DA/B/C/modified PO/DA/B/C/modified PO/D ^/B/C/modified PO/DA /B/C/modified PO/D | a/B/C/modified PO/D ^i/B/C/modified PO/DA/B/C/modified PO/DA/B/C/modified PO/DA/B/C/modified PO/D | A/B/C/modified PO/DA/B/C/modified PO/DA/B/C/modified PO/DA/B/C /modified PO / D | A / B / C / modified PO / D impact resistance 〇〇〇〇〇〇〇〇 <<<< o 〇 ~ △ 〇 ~ △ o 〇 ~ △ 〇 ooo Vibration resistance -3 〇〇〇〇〇〇〇〇<< o Ό~Λ 〇~△ o 〇~△ O ooo Vibration resistance-2 |〇~Δ 〇Vibration resistance-1 Formability|mm Propylene film (D) Young's modulus|MPa inch ir> inch WJ inch 380 500 500 ^00 ^15 415 ; Ul 415 ^15 415 U-) 415 415 | 415 415 415 | 415 Length |655 m \〇li-l in wo Ό in v〇o MX 730 730 |480 | •ο in ^55_I wi VJ? »·〇ir> \〇ΙΛ) Ό Ό »r> to V〇ITi IT5 \ 〇so m 655 iTi vn IT) ΙΛ Ό in in \n in \r> breaking strength [MPa ΙΛ Γ〇in r^) r<li〇r^l Pl o tr> r·) r^) in r·) Yn r^) r^ir〇 alignment nylon 6 film (B) elongation at break |398 398 OO Os r^) 398 398 OO Q\ 398 398 β98 i 00 〇\ ΡΛ 398 398 00 〇s 398 398 00 On OO ON 398 398 | 398 398 398 398 | oo Os breaking strength | MPa S s S ss S s 00 ossss S ss SS ssssss S alignment film (A) elongation at break 00 oo § oo ?] in 215 |2I5 cs 215 ?; V -) ID fq i〇n 215 | 215 215 〇s OO 00 <N OO breaking strength [MPa (275 uo V〇ON in Ό ό v〇Ό 〇SO Ό 2 ·〇Ό IT) VO in v〇ss 5 250 | 232 Alignment M Ί M Ί Ί Ί 轴 Ί Ί Ί Ί Ί Ί Ί Ί Ί Ί PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET丨PET PET PET PET | PET; PET PET PET PET PET PET PET PET PET PET | 1 Example 49 Example 50 Example 51 Example 52 Example 53 Example 54 Example 55 Example 56! Example 57丨Example 58 1 |Example 591 |Example 60 I |Example 6]1 Example 62 |Example 63 1 丨Example 64 1 丨Example 651 Example 66 |Example 67 | |Example 68 |Example 69 I Example 70 | Example 71 I 1 Example 72 1 -09- ls-r(o*«(s®-M concentrated: z3d ISMlo^B-Mi4i554: 13d 201222930 [inch'<;] Laminates|Lamination order| A/B/C/modified PO/D Ia/b/c/pe/d IA/B/C/DA/B/C/modified PO/DA/B/C/ Modified PO/DA/B/C/modified PO/DB/C/D [A/B/C/modified PO/DIB/A/C modified PO/DA/C/B/D ^ modified PO /C/B/D | ^VB/C/modified PO/DA/B/C/PE/DA/B/C/DA/B/C/modified PO/DA/B/C/modified PO/ DA/B/C/modified PO/DB/C/DA/B/C/modified PO/D | B/A/C modified PO/D | impact resistance: 1 vibration resistance-3 | vibration resistance Sex-2 XX XX XX 1 XX XX XX | XX Vibration resistance-1 XX X XX 1 X χ XX XX XX j XX XX @形性 | [mm 1 oo 00 1 卜卜ON 卜<?s 〇\ 〇s Polypropylene film (D) Modulus | MPa 415 W-ϊ 415 3012 |630 630 415 Vi oo »/*> 415 | 415 ^r, 415 415 415 β012 ο m \〇630 Wl <r> oo in 415 1 elongation at break 655 in 655 (N 〇\ |510 ν〇655 500 «·〇ΙΛ SO U*i <ς> J655 655 655 (N ON 510 w-) ui W-) vj-> 500 | in 1 breaking strength [MPa ρη in OO oo 00 卜 »r> 00 U-) r〇r^) »r> r ^) 00 00 oo 00 00 f^) r<) Alignment; Difficult 墀 Ί Difficulty m 瑞碟 m Difficult carbon 5 »1 Carbon 墉 male nylon 6 film (B) I elongation at break I oo ON οη 00 Os CO oo On r1) 00 ON n OO 〇\ oo On oo oo as r<) oo ON Γ*") oo 〇\ ΡΛ -1 oo oo Os oo 〇\ r*1) 398 oo ON oo ON OO 〇\ 398 | oo OS |Fracture Strength | |MPa 1 00 S s S sss SS ss Wear rs SS ss SS ss Alignment Mud 磡 磡 墀璀埦 墀璀埦 磔Ί 磔Ί 埦璀媸墉墀 媸 ( ( ( ( Elongation at break 00 oo 00 00 00 00 00 oo oo oo 00 00 00 00 00 OO OO 1 00 00 1 Degree|MPa 240 240 240 240 [240 o 1 _I o ^4〇_I o 卜 (N 275 JQ 275 jn CN JO rs I JO (N 275 Alignment Two-axis Ί Two-axis two-axis Ί Ί ! Ί Ί Ί \Ξ^\ Ί Ί Ί Ί Ί Ί Ί Ί Ί Ί Ί Ί Ί Ί Ί Ί Ί PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET 1 Comparative Example 2 Comparative Example 3 Comparative Example 4 1 Comparative Example 5 1 | Comparative Example 6 I 丨 Comparative Example 7 1 ft 匕 Comparative Example 8 1 [t匕 Comparative Example 9 | f Comparative Example io| [fc匕 Comparative Example 11] Comparative Example 12 "Comparative Example 13 | Comparative Example 14 [Comparative Example 15 1 Comparative Example 16 | Comparative Example 17 | Comparative Example 18 | Comparative Example 19 | Comparative Example 20 sMo^B--r Spread: z3d IS-ro^BM ^^si: lUJd 敦$铋:〇d 绉 铋玑 铋玑 铋玑 ^ w^is: vcu 留^3⁄4 : vlcu 201222930 [S_I<] Laminate 1 stacking order A/C/modified PO/B/DA/Change PO/C/B/DA/B/C//modified PO/DA/B/C/modified P0/D ^VB/C/modified P0/DA/B/C/modified P0/DA/ B/C/PE/D |a/b/c/d I ^/B/C/modified P0/DA/B/C/modified P0/D ^VB/0/modified P0/D 1 !b /c/d A/B/C/modified P0/DB/A/C/modified P0/DA/C/modified PO/B/DA/modified, f± P0/C/B/DA/B/ C/ P0/DA/B/C/modified P0/DA/B/C/modified P0/D | A/B/C/modified P0/D impact resistance XX XX NX ! X χ XX kx XX XX XX XXXX Vibration resistance-3 XX XX ^<x 1 X χ XX Xx XX p<X Xx XXX y Vibration resistance-2 XX XX XX |xx Vibration resistance-1 Formability 1 Polypropylene film (D) Young Modulus tMPa 415 415 5 415 415 415 ^15_I 3012 沄|63〇_I 00 1/) ^15 ¢15_1 ^15 <n «n 415 Elongation at break · in Ό ITi Ό 655 «·〇in VO IT) So 655 ^55_I <N o IT) <^ί iT) Ό o 655 »·〇κη Ό Ό so Ό ir> »/*» breaking strength|MPa ΙΛ υΊ r<> U-) r*" ID oo 00 oo r*~i 00 in f^) «/>r<)ir>ir> f^| «Ο m | Alignment 璀m 璀5 M Carbon hard disk difficult nylon 6 film (B) Elongation at break 00 σ\ 〇〇On 〇〇〇s 398 |398 u-» 00 398 |398 | oo 〇\ OO σ\ Γη OO σν Γ<Ί 00 ON ^98 398 β98 398 oo ON r*) 398 OO <7\ r^) 398 breaking strength (MPa s S sss CO ss SSS sssssss S s P to carbon 碡 two-axis carbon hard carbon 墀磲 carbon 墀埤 disc carbon film (A > elongation at break 00 00 l〇ON [365 trj 215; IT) n IT) 刁Μ rs 1 215 ID Π «/ ) Ό s〇ms oo Ό o Breaking strength|MPa 275 275 o \〇235 g Ό so in Ό v〇1 »ri m vO tr> VO S r- 〇Ό Ό Alignment two-axis M ff two-axis Ί Axis | \Ξ^\ Ί Ί 轴 二 二 二 二 二 二 二 二 二 二 M M M M M M PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET PET pet|Comparative Example 21 Comparative Example 22 Comparative Example 23 Comparative Example 24 | Comparative Example 25 Comparative Example 26! 丨 Comparative Example 271 | Comparative Example 28] | Comparative Example 29 I Comparative Example 30 丨 Comparative Example 31 1 | Comparative Example 32 1 |Comparative Example 33 | Comparative Example 34 | Comparative Example 35 1 Comparative Example 36 Comparative Example 37 Comparative Example 38 | Comparative Example 39 | Comparative Example 40 SMO^BM 滹铋: z3d isMo?sB-Mi4si54: Idd

Iit-鉍:〇d ¾¾^¾啣米%'7xs: Vd ¾¾ 鉍:Vld s-19_ 201222930 [產業上的利用可能性] 本發明的積層材係加工性良好,由本發明的積層材 所作成的容器係耐藥品性、耐振動性優異,故本發明的 積層材係可適用作為在電動汽車、混合動力汽車、電氣 自動二輪車所搭載的二次電池用容器用之積層材。 【圖式簡單說明】 益 〇 i 【主要元件符號說明】 無。 -63-Iit-铋:〇d 3⁄43⁄4^3⁄4米米%'7xs: Vd 3⁄43⁄4 铋:Vld s-19_ 201222930 [Industrial Applicability] The laminated material of the present invention is excellent in workability and is formed of the laminated material of the present invention. The container is excellent in chemical resistance and vibration resistance. Therefore, the laminated material of the present invention can be suitably used as a laminate for a secondary battery container mounted on an electric vehicle, a hybrid vehicle, or an electric motorcycle. [Simple description of the diagram] Benefits 【 i [Description of main component symbols] None. -63-

Claims (1)

201222930 七、申請專利範圍: 1 · 一種二次電池容器用積層材,農 對苯二甲酸乙二醋、聚萘二甲西依順序積層有由聚 位系芳香族聚醢胺所成的薄膜一能、聚乳酸或對 箱⑹、聚丙浠薄膜⑼之積層材尼龍6薄膜⑻、銘 配向薄膜,8及D係無配向薄膜,其/徵為:八係二軸 改性聚烯烴層,而且D的楊模C與D之間設有 …請專利範圍…之二=為」:_以下。 中該改性聚烯烴層係由接枝 ::用積層材’其 人丨王眾丙烯所成。 3. 如申請專利範圍第丨或2項之_ ·Α # ^ ¥ 、之人電池容器用積層材 ,其中由聚對苯二甲酸乙二醋、聚萘二甲酸乙二酿咬 2礼酸所成的薄膜⑷之斷裂強度為150〜25〇MPa,斷 裂伸長度為100〜150%。 4. 如:請專利範圍第1或2項之二次電池容器用積層材 ,其中由聚對苯二甲酸乙二醋、聚萘二甲酸乙二醋或 對位系芳香族聚醯胺所成的薄膜(A)之斷裂強度為250 〜48〇MPa,斷裂伸長度為80〜170%。 士申明專利範圍第1或2項之二次電池容器用積層材 了中由伞對笨一曱酸乙二酯所成的薄膜(a)之斷裂強 度為100〜250MPa ’斷裂伸長度為170%以上。 6. —種二次電池容器用積層材之製造方法,其特徵為: 依順序積層斷裂強度為15〇〜25〇MPa、斷裂伸長度為 1 00〜1 50%的由聚對苯二曱酸乙二酯、聚萘二曱酸乙二 酉曰或聚乳酸所成的薄膜(A)、無配向的尼龍6薄膜(B) 、鋁油(C),在C與D之間設置改性聚烯烴層,積層揚 氏模數為500MPa以下的無配向之聚丙烯薄膜(D)。 -64- 201222930 7.—種二次電池容器用積層材之製造方法其特徵為: 依順序積層斷裂強度為250〜480MPa、斷裂伸長度為 8 0〜170%的由聚對笨二曱酸乙二酯、聚萘二甲酸乙二 酉曰或對位系芳香族聚醯胺所成的薄膜(A)、無配向的尼 龍6薄膜(B)、銘箔(C),在C與D之間設置改性聚烯 火二層’積層楊氏模數為500MPa以下的無配向之聚丙烯 薄膜(D)。 8 ·種—-人電池容器用積層材之製造方法,其特徵為: 依順序積層斷裂強度為100〜250MPa、斷裂伸長度為 1 7 0 %以上的令e a ^ 公對本二甲酸乙二酯薄膜(A)、無配向的尼 月^ 6薄膜⑻、1呂落(C) ’在c與D之間設置改性聚稀 ^工層積層揚氏模數為500MPa以下的無配向之聚丙稀 薄膜(D)。 8項中任一項之二次電池容器 其中該改性聚烯烴層係由接枝 如申請專利範圍第6至 用積層材之製造方法, 改性聚丙烯所成。 10 矛人電池谷益,其係藉由如申請專利範圍第1至 項中任-項之二次電池容器用積層材所形成。 -65- 201222930 四、指定代表圖: (一) 本案指定代表圖為:無。 (二) 本代表圖之元件符號簡單說明: 益 〇 « 五、本案若有化學式時,請揭示最能顯示發明特徵的化學式:201222930 VII. Scope of application for patents: 1 · A laminate for secondary battery containers, a mixture of ethylene terephthalate and polyethylene naphthalate, with a film formed by poly-glycol aromatic polyamine , polylactic acid or counter-box (6), polypropylene film (9) laminated material nylon 6 film (8), Ming directional film, 8 and D-type unaligned film, which is: octagonal biaxially modified polyolefin layer, and D There is a space between Yang Mo C and D... Please patent range... 2 = ": _ below. The modified polyolefin layer is formed by grafting :: using a laminate material. 3. For example, if you apply for the patent scope 丨 or 2 _ ·Α # ^ ¥, the battery for the battery container, which consists of polyethylene terephthalate or polyethylene naphthalate. The resulting film (4) has a breaking strength of 150 to 25 MPa and an elongation at break of 100 to 150%. 4. For example, please use the laminated material for secondary battery containers of the first or second patent scope, which consists of polyethylene terephthalate, polyethylene naphthalate or para-aramid. The film (A) has a breaking strength of 250 to 48 MPa and an elongation at break of 80 to 170%. The film of the secondary battery container according to the first or second aspect of the patent scope of the invention has a breaking strength of 100 to 250 MPa and a breaking elongation of 170%. the above. A method for producing a laminate for a secondary battery container, characterized in that: a polyphenylene terephthalate having a breaking strength of 15 Å to 25 MPa and an elongation at break of 100 to 1 50% in this order Film (A) made of ethylene glycol, polyethylene naphthalate or polylactic acid, unaligned nylon 6 film (B), aluminum oil (C), modified polycondensation between C and D The olefin layer is an unaligned polypropylene film (D) having a laminated Young's modulus of 500 MPa or less. -64- 201222930 7. A method for producing a laminated material for a secondary battery container, characterized in that: a poly-p-benzoic acid B is formed by sequentially laminating a breaking strength of 250 to 480 MPa and an elongation at break of 80 to 170%. Film (A) made of diester, polyethylene naphthalate or para-aromatic polyamine, unaligned nylon 6 film (B), and foil (C), between C and D An unoriented polypropylene film (D) having a modified polyene fire two layer 'layered Young's modulus of 500 MPa or less is provided. 8 - a method for producing a laminated material for a human battery container, characterized in that: EA ^ male to ethylene glycol diester film is formed by sequentially laminating a breaking strength of 100 to 250 MPa and an elongation at break of 170% or more (A), unaligned Niyue ^ 6 film (8), 1 Lu (C) 'Set a modified poly-layer layer between C and D, the unaligned polypropylene film with a Young's modulus of 500 MPa or less (D). The secondary battery container according to any one of the items 8, wherein the modified polyolefin layer is formed by grafting, as in the method of the sixth aspect of the invention, to a method for producing a laminate. 10 Spearman battery Gu Yu, which is formed by a laminate for a secondary battery container as claimed in any of claims 1 to 3. -65- 201222930 IV. Designated representative map: (1) The representative representative of the case is: None. (2) A brief description of the symbol of the representative figure: Yi 〇 « V. If there is a chemical formula in this case, please disclose the chemical formula that best shows the characteristics of the invention:
TW100120629A 2010-06-15 2011-06-14 A laminated material for secondary battery container and method for manufacturing the same and secondary battery container TW201222930A (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
JP2010135724 2010-06-15
JP2010165606 2010-07-23
JP2010179965 2010-08-11

Publications (1)

Publication Number Publication Date
TW201222930A true TW201222930A (en) 2012-06-01

Family

ID=45348069

Family Applications (1)

Application Number Title Priority Date Filing Date
TW100120629A TW201222930A (en) 2010-06-15 2011-06-14 A laminated material for secondary battery container and method for manufacturing the same and secondary battery container

Country Status (3)

Country Link
JP (1) JPWO2011158662A1 (en)
TW (1) TW201222930A (en)
WO (1) WO2011158662A1 (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN104851992A (en) * 2013-12-19 2015-08-19 通用汽车环球科技运作有限责任公司 System and method for conducting battery heat using pouch cells
TWI842725B (en) * 2018-07-31 2024-05-21 日商尤尼吉可股份有限公司 Polyamide-based laminated film and method for producing same

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP6127394B2 (en) * 2012-06-27 2017-05-17 大日本印刷株式会社 Packaging materials for electrochemical cells
JP6427969B2 (en) * 2014-06-10 2018-11-28 凸版印刷株式会社 Method for manufacturing exterior material for power storage device

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2001229971A (en) * 2000-02-14 2001-08-24 At Battery:Kk Nonaqueous electrolyte secondary battery
JP3719235B2 (en) * 2002-07-08 2005-11-24 日産自動車株式会社 Thin battery, assembled battery, composite assembled battery and vehicle
JP5266628B2 (en) * 2006-08-28 2013-08-21 大日本印刷株式会社 Battery packaging material
JP5114260B2 (en) * 2007-03-30 2013-01-09 大日本印刷株式会社 Packaging material for flat electrochemical cells

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN104851992A (en) * 2013-12-19 2015-08-19 通用汽车环球科技运作有限责任公司 System and method for conducting battery heat using pouch cells
TWI842725B (en) * 2018-07-31 2024-05-21 日商尤尼吉可股份有限公司 Polyamide-based laminated film and method for producing same

Also Published As

Publication number Publication date
WO2011158662A1 (en) 2011-12-22
JPWO2011158662A1 (en) 2013-08-19

Similar Documents

Publication Publication Date Title
KR101947841B1 (en) Molding packaging material and battery case
US10547033B2 (en) Packaging material for batteries, and battery
JP6724483B2 (en) Mold for molding battery packaging material
TWI569969B (en) Packaging material for forming and manufacturing method thereof
CN102431239B (en) Polymer lithium ion battery core outer package forming material
TW201230449A (en) Lithium-ion battery exterior materials
JP5453680B2 (en) Laminated material for secondary battery container, secondary battery container and method for producing secondary battery container
TW201006672A (en) Cover tape for packaging electronic parts and electronic-parts package
JPWO2018097329A1 (en) Battery packaging material, manufacturing method thereof, and battery
JP6074920B2 (en) Packaging materials
JP6990972B2 (en) Exterior material for power storage device and power storage device using it
JP2017069203A (en) Battery-packaging material and battery
JP7306429B2 (en) BATTERY PACKAGING MATERIAL, MANUFACTURING METHOD THEREOF, AND BATTERY
JP2019029300A (en) Battery-packaging material, method for manufacturing the same, and battery
TW201222930A (en) A laminated material for secondary battery container and method for manufacturing the same and secondary battery container
JP2017120790A (en) Adhesive film for tightly sealing metal terminal portion of electricity storage device
WO2021006350A1 (en) Adhesive film for metal terminal, metal terminal with adhesive film for metal terminal, power storage device using said adhesive film for metal terminal, and method for producing power storage device
JPWO2017188445A1 (en) Battery packaging material and battery
JP5424176B2 (en) Laminated material for secondary battery container and secondary battery container
JP2012059379A (en) Laminate material for secondary battery container, and secondary battery container
JP6954437B2 (en) Adhesive film for metal terminals, method for manufacturing adhesive film for metal terminals, metal terminal with adhesive film for metal terminals, power storage device using the adhesive film for metal terminals, and method for manufacturing power storage device
JP6882617B1 (en) Adhesive film for metal terminals, method for manufacturing adhesive film for metal terminals, metal terminal with adhesive film for metal terminals, power storage device using the adhesive film for metal terminals, and method for manufacturing power storage device
JP6015134B2 (en) Packaging materials
JP6699130B2 (en) Battery packaging material
WO2021201214A1 (en) Adhesive film for metal terminal, production method for adhesive film for metal terminal, metal terminal with adhesive film for metal terminal, power storage device, and production method for power storage device