TW200920811A - Resin film with adhesive and optical laminate using the same - Google Patents

Resin film with adhesive and optical laminate using the same Download PDF

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Publication number
TW200920811A
TW200920811A TW097133062A TW97133062A TW200920811A TW 200920811 A TW200920811 A TW 200920811A TW 097133062 A TW097133062 A TW 097133062A TW 97133062 A TW97133062 A TW 97133062A TW 200920811 A TW200920811 A TW 200920811A
Authority
TW
Taiwan
Prior art keywords
film
adhesive
resin film
resin
weight
Prior art date
Application number
TW097133062A
Other languages
Chinese (zh)
Other versions
TWI529230B (en
Inventor
Sung-Min Kim
Ji-Hye Heo
Han-Young Choi
Original Assignee
Sumitomo Chemical Co
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Filing date
Publication date
Application filed by Sumitomo Chemical Co filed Critical Sumitomo Chemical Co
Publication of TW200920811A publication Critical patent/TW200920811A/en
Application granted granted Critical
Publication of TWI529230B publication Critical patent/TWI529230B/en

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    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J133/00Adhesives based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Adhesives based on derivatives of such polymers
    • C09J133/04Homopolymers or copolymers of esters
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J133/00Adhesives based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Adhesives based on derivatives of such polymers
    • C09J133/04Homopolymers or copolymers of esters
    • C09J133/06Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, the oxygen atom being present only as part of the carboxyl radical
    • C09J133/062Copolymers with monomers not covered by C09J133/06
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J133/00Adhesives based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Adhesives based on derivatives of such polymers
    • C09J133/04Homopolymers or copolymers of esters
    • C09J133/06Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, the oxygen atom being present only as part of the carboxyl radical
    • C09J133/062Copolymers with monomers not covered by C09J133/06
    • C09J133/066Copolymers with monomers not covered by C09J133/06 containing -OH groups
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J7/00Adhesives in the form of films or foils
    • C09J7/30Adhesives in the form of films or foils characterised by the adhesive composition
    • C09J7/38Pressure-sensitive adhesives [PSA]
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J7/00Adhesives in the form of films or foils
    • C09J7/30Adhesives in the form of films or foils characterised by the adhesive composition
    • C09J7/38Pressure-sensitive adhesives [PSA]
    • C09J7/381Pressure-sensitive adhesives [PSA] based on macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
    • C09J7/385Acrylic polymers
    • GPHYSICS
    • G02OPTICS
    • G02BOPTICAL ELEMENTS, SYSTEMS OR APPARATUS
    • G02B5/00Optical elements other than lenses
    • G02B5/30Polarising elements
    • G02B5/3025Polarisers, i.e. arrangements capable of producing a definite output polarisation state from an unpolarised input state
    • GPHYSICS
    • G02OPTICS
    • G02BOPTICAL ELEMENTS, SYSTEMS OR APPARATUS
    • G02B5/00Optical elements other than lenses
    • G02B5/30Polarising elements
    • G02B5/3025Polarisers, i.e. arrangements capable of producing a definite output polarisation state from an unpolarised input state
    • G02B5/3033Polarisers, i.e. arrangements capable of producing a definite output polarisation state from an unpolarised input state in the form of a thin sheet or foil, e.g. Polaroid
    • G02B5/3041Polarisers, i.e. arrangements capable of producing a definite output polarisation state from an unpolarised input state in the form of a thin sheet or foil, e.g. Polaroid comprising multiple thin layers, e.g. multilayer stacks
    • G02B5/305Polarisers, i.e. arrangements capable of producing a definite output polarisation state from an unpolarised input state in the form of a thin sheet or foil, e.g. Polaroid comprising multiple thin layers, e.g. multilayer stacks including organic materials, e.g. polymeric layers
    • GPHYSICS
    • G02OPTICS
    • G02FOPTICAL DEVICES OR ARRANGEMENTS FOR THE CONTROL OF LIGHT BY MODIFICATION OF THE OPTICAL PROPERTIES OF THE MEDIA OF THE ELEMENTS INVOLVED THEREIN; NON-LINEAR OPTICS; FREQUENCY-CHANGING OF LIGHT; OPTICAL LOGIC ELEMENTS; OPTICAL ANALOGUE/DIGITAL CONVERTERS
    • G02F1/00Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics
    • G02F1/01Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour 
    • G02F1/13Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour  based on liquid crystals, e.g. single liquid crystal display cells
    • G02F1/133Constructional arrangements; Operation of liquid crystal cells; Circuit arrangements
    • G02F1/1333Constructional arrangements; Manufacturing methods
    • G02F1/1335Structural association of cells with optical devices, e.g. polarisers or reflectors
    • G02F1/13363Birefringent elements, e.g. for optical compensation
    • G02F1/133632Birefringent elements, e.g. for optical compensation with refractive index ellipsoid inclined relative to the LC-layer surface
    • GPHYSICS
    • G02OPTICS
    • G02FOPTICAL DEVICES OR ARRANGEMENTS FOR THE CONTROL OF LIGHT BY MODIFICATION OF THE OPTICAL PROPERTIES OF THE MEDIA OF THE ELEMENTS INVOLVED THEREIN; NON-LINEAR OPTICS; FREQUENCY-CHANGING OF LIGHT; OPTICAL LOGIC ELEMENTS; OPTICAL ANALOGUE/DIGITAL CONVERTERS
    • G02F1/00Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics
    • G02F1/01Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour 
    • G02F1/13Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour  based on liquid crystals, e.g. single liquid crystal display cells
    • G02F1/133Constructional arrangements; Operation of liquid crystal cells; Circuit arrangements
    • G02F1/1333Constructional arrangements; Manufacturing methods
    • G02F1/1335Structural association of cells with optical devices, e.g. polarisers or reflectors
    • G02F1/13363Birefringent elements, e.g. for optical compensation
    • G02F1/133633Birefringent elements, e.g. for optical compensation using mesogenic materials
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J2203/00Applications of adhesives in processes or use of adhesives in the form of films or foils
    • C09J2203/318Applications of adhesives in processes or use of adhesives in the form of films or foils for the production of liquid crystal displays
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J2301/00Additional features of adhesives in the form of films or foils
    • C09J2301/30Additional features of adhesives in the form of films or foils characterized by the chemical, physicochemical or physical properties of the adhesive or the carrier
    • C09J2301/302Additional features of adhesives in the form of films or foils characterized by the chemical, physicochemical or physical properties of the adhesive or the carrier the adhesive being pressure-sensitive, i.e. tacky at temperatures inferior to 30°C
    • GPHYSICS
    • G02OPTICS
    • G02FOPTICAL DEVICES OR ARRANGEMENTS FOR THE CONTROL OF LIGHT BY MODIFICATION OF THE OPTICAL PROPERTIES OF THE MEDIA OF THE ELEMENTS INVOLVED THEREIN; NON-LINEAR OPTICS; FREQUENCY-CHANGING OF LIGHT; OPTICAL LOGIC ELEMENTS; OPTICAL ANALOGUE/DIGITAL CONVERTERS
    • G02F2201/00Constructional arrangements not provided for in groups G02F1/00 - G02F7/00
    • G02F2201/50Protective arrangements
    • GPHYSICS
    • G02OPTICS
    • G02FOPTICAL DEVICES OR ARRANGEMENTS FOR THE CONTROL OF LIGHT BY MODIFICATION OF THE OPTICAL PROPERTIES OF THE MEDIA OF THE ELEMENTS INVOLVED THEREIN; NON-LINEAR OPTICS; FREQUENCY-CHANGING OF LIGHT; OPTICAL LOGIC ELEMENTS; OPTICAL ANALOGUE/DIGITAL CONVERTERS
    • G02F2202/00Materials and properties
    • G02F2202/28Adhesive materials or arrangements

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  • Physics & Mathematics (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Nonlinear Science (AREA)
  • General Physics & Mathematics (AREA)
  • Optics & Photonics (AREA)
  • Mathematical Physics (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Adhesives Or Adhesive Processes (AREA)
  • Polarising Elements (AREA)
  • Adhesive Tapes (AREA)

Abstract

Provided is a resin film with adhesive, having an adhesive layer, which has high antistatic properties without varying with passage of time and excellent durability, provided on a surface of a resin film. An adhesive layer is formed on at least one surface of a resin film such as optical film and surface protection film, to be provided as a resin film with adhesive. The adhesive is formed of a composition containing 0.2 to 8 weight parts of ionic compound (B) having organic cations, which is solid in room temperature, with respect to 100 weight parts of acrylic resin (A) including a structure unit derived from a (meth) acrylic acid ester represented by the following formula (I) as a main component. (wherein R1 represents hydrogen atom or methyl group, R2 represents C1-14 alkyl group or aralkyl group which may be substituted by C1-10 alkoxy group respectively.)

Description

200920811 九、發明說明: 【發明所屬之技術領域】 本發明是有關形成有黏著劑層之樹脂膜者。在本笋明 中,作為對象之樹脂膜係例如可列舉如:含有偏光膜 或相位差膜的光學膜、或在與該光學膜之黏著劑層為相反 側之面上貼合而直到使用為止都保護著此表面的I面保護 膜。本發明同時亦有關使用形成有此黏著劑層之樹脂膜而 成的液晶顯示用之光學積層體。 f * 【先前技術】 偏光膜是安裝在液晶顯示裝置上而被廣泛使用,在偏. 光片(polarizer)之兩面積層有透明保護膜,至少在一方之保 護膜的表面形成黏著劑層,而以在此黏著劑層上貼著_ 膜的狀態來流通。另外,有時亦在偏光片之兩面貼著有保 護膜的《之偏細m目位差料崎層而製成擴圓 偏光膜,並在此相位差膜側依序貼著黏著劑層/剝離膜。再 L者,亦有在相位差獻表面依序㈣黏著劑層/卿膜之情 形。在貼合於液晶單元(liquid crystal cell)前,從此等偏光 艇、橢圓偏光膜、相位差膜等剝去剝離膜,變成隔著已露 出之黏著劑層而貼合於液晶單元。如此之偏光膜、擴圓偏 光膜或相位差膜,係由於在剝去剝離膜並貼 g單 時會產生靜電,錢㈣望開發有關此現象之防止對= 作為此對策之一者,在曰本專利第3012860號公報中. 揭不在偏光片膜之表面上積層有保護膜且在保護膜之表面 上設置有黏著劑層的偏光膜中,作為黏著劑者,係使用含 320560 6 200920811 '有由電解質鹽與有機聚矽氧烷 -丙婦酸系共聚合物的組成物。雖=:導電性組成物及 -而可表現抗靜f性,㈣ H由使用如此之黎著劍 久性方面也難謂具有充分之性能。 。1195二亍2〇04-53694。號公報 _2_ 叫係揭不在感壓接 =4::4_6:,揭_著二有= 、 '及釦陽離子與含氟原子之声離子所忐Μ 鹽,而可賦予抗靜電性。再者 4±』子所成的 號公報中,揭示在黏著劑3有咖 體之離子性液體,圖謀使並皿(25c)下會成為液 劑之偏光膜若放置長時間几2。然而’經塗布黏著 等間則會由於經時變化而使抗靜電 ^ 1的偏歧之流通及保管期_從製作_ =Γ!月左右之程度,因此,要求在直到顧客:用 ’、々間鲍保持抗靜電性能。 層側::在附黏著劑之光學膜,雖是以其黏著劑 隨著光學膜之尺寸變化錄加熱與冷卻時、 光學膜與黏卿:層可 处合吝, 或黏著劑層與液晶單元玻璃之間可 ^子起或剝落等現象,因此,亦要求不會產生如此 ?不:合現象、且要求耐久性優良。再者,在曝露於高严 日守’作用於光學膜之殘留應力的分布會變成不均勻,在光 320560 7 200920811 學膜之外周部引起應力集中,結果,在黑顯示時因外周部會 ;艾白而產生所「白點狀缺色」之現象,或會產生顏色不均 -之現象,因而也要求抑制如此之「白點狀缺色」或「顏色 不之技術。再者,將附黏著劑之光學膜貼合在液晶單 元時,在有不完備之處時,雖然是將此光學膜先一旦2離 後’再度重貝占新之膜,但當進行此剝離時黏著劑層合隨光 學膜而被劍離,故要求在單元玻璃上不會殘留點著^,且 不會赵檝垢等現象,亦即也要求所謂重加工性(rework)。 判面’表面保護膜一般是隔著形成在其單面之黏 ::而貼:於作為被保護體之光學膜等,用編 =加工或在搬運時產生之損傷或污染等。例如,適用於 之偏_或相位差膜等光學膜’係以防止損 心4作為目的’在與上述用於貼合至液晶單元之黏 者劑層為相反側的面上,以貼著兮 " :離==;雖然是在光學媒貼合於液晶單元後會被 # ^ 订此制離.時’會發生靜電,若在此靜電 晶分子之配向或產液曰曰早几,則.可能會有損害到液 護膜上與Μ ί 缺損的問題發生,放在表面保 «隻膜上户'%各種之抗靜電處理。 由將===供—種附黏著劑之樹一 ^ 久性二二同時此抗靜電性不易經時變化且耐' 明人等為'了解置在該樹脂膜之表面而成。本發 對於以丙烯酸系樹脂作為主 果,舍現相 夂之黏者劑,調配在室溫 320560 8 200920811 (2 5C)下會成為固體之特定 :成物設置在樹腊膜之表面以玲3物’並藉由將此组 :電性、抗靜電性之經時變化及耐’而可得到抗靜 脂膜,而達成本發明。 ‘"之附黏著劑之樹 【發明内容】 本發明人等為了達成相關目的而進行專* 果,發現黏著劑之主成八& 研九之結 八工m 丙婦酸系樹脂係由且有牿定夕 置及/刀子量分你者所構成,並調配特定2種類作 聯劑,再調配具有特定官_其 種類作為父 .#丄 才疋吕此基的寡聚合物作為矽烷化人 ’藉由將以該等而成之黏著·成 : 設置在光學膜之表面,即可得到優異之結果1者黯 也就是說,依據本获明g 丨 r , x P 附黏著劑之樹脂膜, /、係在u脂膜之至少單面上 、 由合f 丁、+.Λ、WA、 乂风铂者剤層,此黏著劑層係 由3有下述成分(A)及(B)之組成物所形成: ㈧以源自下式⑴所示之(子基)丙稀酸構為 主成Μ㈣㈣^ 霉早凡作為 分-。-r2 0 (I) ch2=^1( (式中,心表示氫原子‘曱基,R2表示可分別經碳數丨至 10之燒氧基所取代之碳數U 14的烧基或芳録);以及 (B)具有有機陽離子且在室溫中為'固體的離子性化合物0.2 至8重量份。., 在如此之本發明中,對於構成黏著劑之丙烯酸系樹脂 320560 200920811 ’ 斤為固體之離子性化合物⑻係特別有效 .•劍:二=劑且其不但可賦予由該峨彳所形成之黏著 \匕抗4性’且同時可料謀求抑制抗靜電性的經時變 或相之黏著劑層的樹脂膜,可為含有偏光膜及/ 一 、之光學膜。另外,亦可為在與如此之光Μ膜 黏著劑層為相反側之面上所貼人而之先予膜之 此表面的表面保護膜。而直到使用為止都保護著 板,光學膜時,以其黏著劑層側積層於玻璃基 亦可提二 晶顯示用之光學積層體。於是,依本發明 :種光學積層體,其係在光學膜上形成上述黏著 以其黏著劑層側積層於並使該附黏著劑之光學膜 【實施方.式】曰於破璃基板,而形成光學積層體。 在樹本發明。本發明之附黏著劑之樹脂膜係 ^ ^ T it ® ^ ^# ^ ^ ^ ^ 5 Ϊ^ ^ ^ ^ 3有下述(Α)及(Β)之組成物所形成: (Α)丙卸酸系樹脂,以及 ⑻=機_子且在室溫中為固體之離子性化合物。 「品/先’說明有關構成黏著晚成物之各成分。 [丙烯酸系樹脂(Α)]. 合风刀 本發明之附黏著劑之樹脂膜 — 的結構單元作為主成分者,之(曱基)丙稀酸酉旨 〜體上,除了含有源自該(曱基) 320560 10 200920811 '丙烯酸酯的結構單元之外,可含有源自具備以游離羧基、 羥基、胺基、%氧環為代表之雜環基等極性官能基的單體 ,(較佳為具有極性官能基之(甲基)丙烯酸系化合物)的結構 單一者在此(甲基)丙細酸係指丙稀酸或甲基丙稀酸之 任何一者的意思,其他,例如稱為(甲基)丙烯酸酯等之時 的「(甲基)」也為同樣之意義。 成為丙烯酸系樹脂(A)之主要結構單元的前述式(1) ,中,Rl為氫原子或甲基,尺2是碳數1至14的烷基或芳烷 基,較佳是烷基。關於&所表示之烷基或芳烷基,各個基 中之氫原子亦可經碳數i至1〇之烷氧基所取代。 式⑴所表不之(甲基)丙烯酸酯,具體上,可例示:如 丙烯S欠甲酯、丙烯酸乙酯、丙烯酸丙酯、丙烯酸正丁酯、 丙烯酸正辛g旨、丙稀酸十二_等直鏈狀丙雜燒基醋; 如丙烯酸異丁酯、丙烯酸2_乙基己酯、丙烯酸異辛酯等分 枝狀丙烯酸烷基酯;如曱基丙烯酸曱酯、甲基丙烯酸乙酯、 c曱基丙烯酸丙酯、甲基丙烯駿正丁酯、甲基丙稀酸正辛酯、 甲基丙烯馱十一烷酯等直鏈狀甲基丙烯酸焼基酯;如甲基 丙烯酸異丁酯、甲基丙烯酸2_乙基己酯、甲基丙稀酸異辛 醋專分枝狀甲基丙締酸燒基酯等。 I為經烷氧基取代之烷基時,亦即,R2為烷氧基烷基 夺作為式⑴所示之(甲基)丙稀酸醋者,具體上,例示如 丙,酉夂2-甲氧基乙醋、丙婦酸乙氧基甲醋、甲基丙婦酸 甲氧基乙酯、甲基丙烯酸乙氧基甲酯等。R2為芳烷基時, 作為式(1)所示之(甲基)丙烯酸醋者,具體上,例示如丙稀 320560 11 200920811 酸卞醋、或甲基丙稀酸节i旨等。 • 此等(甲基)丙烯酸酯,可各別單獨使用,亦可使用不 ,同之複數個(甲基)丙烯酸酯而共聚合。 作為具有極性官能基之單體之例子,可列舉:如丙稀 酸、甲基丙烯酸、丙烯酸yj-絲乙醋等具有游離羧基的單 體;如(甲基)丙稀酸2-經基乙醋、(甲基)丙_2_經基丙 醋、(甲基)丙烯酸2-或3-氯經基丙酯、二乙二醇單(甲 基)丙晞酸醋等具有經基的單體;丙婦酿基嗎淋、乙稀基己 内醯胺、N-乙烯基_2_π比嘻烧酉同、(甲基)丙稀酸四氯咬喃基 ^己内醋改質丙烯酸四氫Μ基醋、(甲基)丙稀酸3,4_ 基環己基甲酯、(甲基)丙烯酸縮水甘油醋、2,5_二氫吱 .南等具有雜壞基的單體;如(甲基)丙烯酸ν,ν_二甲基胺基 乙5旨等具有與雜料同之絲的單體等。此等 二200920811 IX. Description of the Invention: [Technical Field of the Invention] The present invention relates to a resin film in which an adhesive layer is formed. In the present invention, the resin film to be used is, for example, an optical film containing a polarizing film or a retardation film, or bonded to the surface opposite to the adhesive layer of the optical film until use. Both sides of the surface protect the protective film. The present invention also relates to an optical layered body for liquid crystal display using a resin film on which the adhesive layer is formed. f * [Prior Art] The polarizing film is widely used by being mounted on a liquid crystal display device, and has a transparent protective film on two areas of a polarizer, and an adhesive layer is formed on at least one of the protective films. The _ film is placed on the adhesive layer to circulate. In addition, a polarizing film may be formed on both sides of the polarizer with a protective film, and a polarizing film may be formed on the retardation film side. Release the film. In addition, there are also cases in which the surface difference is in the order of (4) adhesive layer/clear film. The release film is peeled off from the polarizing boat, the ellipsic polarizing film, the retardation film or the like before being bonded to the liquid crystal cell, and is bonded to the liquid crystal cell via the exposed adhesive layer. Such a polarizing film, a circularly polarizing film, or a retardation film is caused by the generation of static electricity when the peeling film is peeled off and the sheet is affixed, and the prevention of this phenomenon is expected to be developed as one of the countermeasures. In Japanese Patent No. 3012860, a polarizing film in which a protective film is laminated on the surface of the polarizer film and an adhesive layer is provided on the surface of the protective film is used as an adhesive, and the use of 320560 6 200920811 ' A composition of an electrolyte salt and an organopolyoxane-propionic acid copolymer. Although =: conductive composition and - can be expressed anti-static, (4) H is also difficult to say that it has sufficient performance in terms of durability. . 1195 2亍2〇04-53694. Bulletin _2_ Called the system is not pressure sensitive connection =4::4_6:, _ _ two have =, 'and deduction cations and fluoride atomic sound ions, and can give antistatic properties. Further, in the publication of the Japanese Patent Publication No. 4, the ionic liquid having a coffee body in the adhesive 3 is disclosed, and the polarizing film which will become a liquid under the dish (25c) is placed for a long time. However, in the case of the application of the adhesive, etc., the distribution of the anti-static ^ 1 eccentricity and the storage period _ from the production _ = Γ 月 月 月 , , 要求 顾客 顾客 顾客 顾客 顾客 顾客 顾客 顾客 顾客 顾客 顾客 顾客 顾客 顾客 顾客 顾客 顾客 顾客 顾客 顾客 顾客 顾客 顾客The abalone maintains antistatic properties. Layer side:: In the optical film with adhesive, although the adhesive is heated and cooled as the size of the optical film changes, the optical film and the adhesive layer can be combined, or the adhesive layer and the liquid crystal cell There is a phenomenon in which the glass can be lifted or peeled off. Therefore, it is also required that such a phenomenon does not occur, and the durability is required to be excellent. Furthermore, the distribution of the residual stress acting on the optical film exposed to high-strength is becoming uneven, and stress concentration is caused in the outer periphery of the film in the light 320560 7 200920811, and as a result, the outer peripheral portion is formed in the black display; Ai Bai produces the phenomenon of "white spotted lack of color", which may cause color unevenness - and therefore requires suppression of such "white spotted lack of color" or "colorless technology. In addition, it will be attached When the optical film of the adhesive is attached to the liquid crystal cell, when there is an incompleteness, although the optical film is first removed, the film is again re-boiled, but the adhesive is laminated when the peeling is performed. With the optical film being separated by the sword, it is required that there will be no residue on the unit glass, and there will be no phenomenon such as smashing, that is, the so-called rework is also required. The surface protection film is generally It is attached to the optical film which is formed on the one side of the film, and is attached to the optical film or the like which is the protected body, and is damaged or contaminated by the processing or the conveyance. For example, it is suitable for the partial or retardation film. The optical film 'is used to prevent damage 4 as the purpose' The above-mentioned adhesive layer for bonding to the liquid crystal cell is on the opposite side of the surface to be attached to the 兮": ==; although the optical medium is attached to the liquid crystal cell, it will be ordered by the #^ When 'electrostatic electricity will occur, if the alignment or liquid production of the electrostatic crystal molecules is earlier, there may be damage to the liquid film and Μ ί defects, placed on the surface of the film Household '% of various antistatic treatment. From the === supply of a kind of adhesive to the tree of a long-lasting two-two at the same time this antistatic property is not easy to change over time and resistant to 'Mingren et al' to understand the resin It is made of the surface of the film. The hair is made of acrylic resin as the main fruit, and the adhesive is prepared at room temperature 320560 8 200920811 (2 5C). The product is set in the tree wax. 'The surface of the film is made of Ling's and the anti-static film can be obtained by changing the group and the resistance of the group to the electrical and antistatic properties. The invention is achieved. '" SUMMARY OF THE INVENTION The present inventors have made special effects in order to achieve a related purpose, and found that the main component of the adhesive is eight & The eight-work m-type propylene-glycol-based resin consists of the sputum and the knives, and the specific two types are used as the jointing agent, and the specific official _ its type is used as the parent. #丄才疋The oligopolymer of the ruthenium group acts as a ruthenium-based person by providing the adhesion to the surface of the optical film to obtain an excellent result, that is, according to the present invention丨r , x P A resin film with an adhesive, /, on at least one side of the u-lipid film, consisting of a layer of 丁, +.Λ, WA, 乂风铂, the layer of adhesive is 3 The composition of the following components (A) and (B) is formed: (8) The (sub)acrylic acid structure represented by the following formula (1) is mainly composed of ruthenium (tetra) (tetra) and mildew. -r2 0 (I) ch2=^1 (wherein the heart represents a hydrogen atom 'sulfonyl group, and R2 represents a carbon number U 14 which can be substituted by an alkoxy group having a carbon number of 10 to 10, respectively. And (B) 0.2 to 8 parts by weight of an ionic compound having an organic cation and being 'solid at room temperature.', in the present invention, for the acrylic resin constituting the adhesive 320560 200920811 ' The ionic compound (8) is particularly effective. • Sword: two agents, which not only impart adhesion to the crucible formed by the crucible, but also tend to suppress the antistatic property over time or phase. The resin film of the adhesive layer may be an optical film containing a polarizing film and/or an optical film which is attached to the surface opposite to the coating layer of the optical film. The surface protective film on the surface, and the plate is protected until use, and when the optical film is laminated on the glass substrate, the optical layered body for the two crystal display can be extracted. Thus, according to the invention: a layered body formed on the optical film to form the above-mentioned adhesive layer on the side of the adhesive layer The optical film of the adhesive is applied to the glass substrate to form an optical laminate. In the present invention, the resin film of the adhesive of the present invention is ^ ^ T it ® ^ ^# ^ ^ ^ ^ 5 Ϊ^ ^ ^ ^ 3 The following composition of (Α) and (Β) is formed: (Α)Acrylic acid resin, and (8) = machine_subunit and solid ion at room temperature "product / first" describes the components constituting the adhesive late product. [Acrylic resin (Α)]. The air-shielding resin film of the present invention is a main component of the resin film. (曱基)Acrylic acid 〜 〜 体 体 体 体 体 体 体 体 体 体 体 320 320 320 320 320 320 320 320 320 320 320 320 320 320 320 320 320 320 320 320 320 320 320 320 320 320 320 320 320 320 320 320 320 320 a monomer having a polar functional group such as a heterocyclic group represented by a ring, (preferably a (meth)acrylic compound having a polar functional group) has a single structure, and (meth)propionic acid means acrylic acid. Or any of methyl methacrylate, other, for example, when it is called (meth) acrylate, etc. "(Methyl)" is also the same meaning. In the above formula (1) which is the main structural unit of the acrylic resin (A), R1 is a hydrogen atom or a methyl group, and the rule 2 is an alkyl group having 1 to 14 carbon atoms. Or a arylalkyl group, preferably an alkyl group. With respect to the alkyl group or the aralkyl group represented by &, the hydrogen atom in each group may be substituted by an alkoxy group having a carbon number of i to 1 Å. The (meth) acrylate is specifically exemplified by, for example, propylene S owes methyl ester, ethyl acrylate, propyl acrylate, n-butyl acrylate, acrylic acid n-octyl, acrylic acid twelfth, etc. Chain-like propylene ketone; a branched alkyl acrylate such as isobutyl acrylate, 2-ethylhexyl acrylate or isooctyl acrylate; such as decyl methacrylate, ethyl methacrylate, c曱Linear methacrylate methacrylate such as propyl acrylate, methacrylic acid n-butyl acrylate, n-octyl methacrylate, methacrylic acid undecyl ester; such as isobutyl methacrylate, A 2-ethylhexyl acrylate, isooctyl methacrylate, and branched methacrylic acid alkyl ester. When I is an alkyl group substituted with an alkoxy group, that is, R 2 is an alkoxyalkyl group, which is a (meth) acrylate vinegar represented by the formula (1), specifically, for example, C, 酉夂2- Methoxyacetic acid, ethoxyethyl ethoxyacetate, methoxyethyl methacrylate, ethoxymethyl methacrylate, and the like. When R2 is an aralkyl group, the (meth)acrylic acid vinegar represented by the formula (1) is specifically exemplified by propylene 320560 11 200920811 citric acid vinegar or methyl methacrylate. • These (meth) acrylates may be used singly or in combination with a plurality of (meth) acrylates. Examples of the monomer having a polar functional group include a monomer having a free carboxyl group such as acrylic acid, methacrylic acid or acrylic acid yj-silk vinegar; for example, (meth)acrylic acid 2-base group B Vinegar, (meth)propan-2-p-propyl acetonate, 2- or 3-chloropropyl methacrylate, diethylene glycol mono(methyl) propyl citrate, etc. Body; B-branched base, ethyl hexylamine, N-vinyl 2_π than bismuth, (methyl) acrylic acid tetrachloro-brown base ^ hexane vinegar modified tetrahydrogen acrylate Mercapto vinegar, (meth)acrylic acid 3,4-cyclohexyl methyl ester, (meth)acrylic acid glycidol vinegar, 2,5-dihydroanthracene, south, etc. having a heterogeneous group; The base acrylate, ν-dimethylaminoethylene 5 or the like has a monomer or the like which is the same as the rayon. These two

能基^體各驗單獨制,也可使料;Γ複數者I 〜中,較佳係將具有羥基單用、 酸系樹⑽)之含有極性官A 用於作為構成丙* 古〜甘乂 另性注吕此基的早體之一。同時,除了且 經基之早體之外,併用其他之 性單例 如具有游離《單體)亦為有效。 基之早體(例 在黏著劑層中所使用的丙烯 +八· 揮發分HK)重量份,前、系树脂⑷’相對於其不 的社構單元,甬2 源自式(1)所示之(甲基)丙烯酸酯 重量份)之比率含m 重!伤(較佳為80至99.6 結構單元通常是以0」至2〇番旦二"生吕-基之早體的 份)之比率含有。里刀(較佳為〇.4至重量 320560 12 200920811 本么明中所使用之丙烯酸系樹脂(A),亦可含有源自除 了上述之式⑴之(甲基)丙烯酸酯及具有極性官能基之單體 以=之單體的結構單元。作為此等之例者可列舉如:源自 在刀子内具有脂裱式結構之($基)丙烯酸酯的結構單元、 ^自苯乙料單體的結構單元、源自乙烯基系單體的結構 皁兀、源自在分子内具有複數個(甲基)丙婦醯基 結構單元等^ 干股的 作為知環式結構者,係碳數通常在5以上(較佳為$至 7左右)之環垸(eyelGparaffin)結構。具有脂環式結構的丙稀 酸酯之具體例,可列舉如:丙婦酸異細、丙婦酸環己 酉曰丙烯I —裱戊酯、丙烯酸環十二烷酯v丙烯酸甲美環 己醋、丙烯酸三甲基環己酯、丙烯酸第三丁基環己酯、 乙氧基丙烯酸環己酯、丙烯酸環己基苯酯等,具有脂環式 結構的甲基丙烯酸醋之具體.例,可列舉如:甲基丙烯酸; 冰片酯、甲基丙烯酸環己酯、甲基丙烯酸二環戊醋、甲美 丙烯酸環十二烧醋、甲基丙烯酸甲基環己§|、甲基丙烯ς ^甲基環己醋、甲基丙烯酸第三丁基環己醋、甲基丙婦酸 壤己基苯酿等.。 作為苯乙烯系單體的例子,除了苯乙烯之外,可列舉 ^ ··如甲基苯乙烯、二甲基苯乙烯、三甲基苯乙烯、乙基 苯?烯、二乙基苯乙烯、三乙基苯乙烯、丙基苯乙烯、; ,苯乙烯、己基苯乙烯、庚基苯乙烯、辛基苯乙蝉等烧基 苯乙烯氟化苯乙烯、氯化苯乙烯、溴化苯乙稀、二、、臭 化苯乙稀、硬化苯乙烯等幽化苯乙稀;再者,如硝基苯乙 320560 13 200920811 •.烯、乙醯基苯乙烯、甲氧基苯乙烯、二乙烯基苯等。 • 乙稀基系單體之例子可列舉:如乙酸乙烯酯、丙酸乙 .烯s曰、丁酸乙烯酯、2_乙基己酸乙烯酯、十二烷酸乙烯酯 等月曰肪酉夂乙婦g旨,如氣化乙烯他⑽他)或漠化乙烯 專鹵化乙稀,如偏—氯乙烯(vinyiene chi〇ride)等偏二鹵化 乙烯,如乙烯基吡啶、乙烯基吡咯烷酮、乙婦基咔唑等含 氮之专Ϊ族乙稀;如丁二烯、異戊二烯、氯化戊二稀等共 輛一烯單體,再者,可列舉如丙烯腈、甲基丙烯腈等。 .分子内具有複數個(甲基)丙烯醯基之單體之例子可列 舉.如1,4_丁二醇二(甲基)丙烯酸酯、^二 丙稀酸醋…二醇二(甲基)丙稀酸醋'乙二== 丙烯H —乙二醇二(甲基)丙烯酸醋、四乙 丙烯酸酯、三丙二醇甲翼、品κ * 哔一 π丞) 個__基之二 西旨箄在八甲基丙烧三(甲基)丙婦酸 酉曰專在刀子内有3個(甲基)丙烯醯基之單體等。 '以外ti(I)之(甲基)丙稀酸醋及具有極性官能基之單體 ^ ^ ^ 5 ^ ^ ^ ^ ^ ^ ^ ^ ^ 2 ^ ^ ^ ^ ^ ^ 0 ^ ^(1)^ 一土)丙Mi旨及具極性官能基之單體以外之單體 m對於該樹贿不揮發分_重量份,通θ = 至20二量份(較佳為0至」。重量份)之比率含有 丙婦酸酯的結構單元作為主成分,二3 =之(甲基) 源自具有極性官能基之單體的块構:了3有2種以上包含 。構早兀之丙婦酸系樹脂。 320560 14 200920811 '再者,在前述丙烯酸系樹脂令,亦可混合有與豆不同之丙 :烯酸系樹腊(具體上,例如具有源自式⑴之(甲基)丙烯酸酯 .的結構皁元且不含極性官能基的㈣酸系樹料)。以源自 式⑴之(曱基)丙蝉酸醋的結構單元作$主成分且含有源自 具有極性官能基之單體的結構單元之丙稀酸系樹脂,係在 丙_系樹脂全體之中,佔60重量%以上,更好為佔8〇 重量%以上者。 ㈣自式(1)之(甲基)丙烯酸g旨之結構單㈣為主成分 且含㈣自具有極性宫能基之單體的結構單元之丙稀酸系 树脂,錯由凝膠滲透層析(GPC)法換算成標準聚苯乙稀的 重量平均分子量(Mw)係以在,㈣之範圍 者為佳。換算成標準聚苯乙烯的重量平均分子量在 1’0:0,000以上時’因高溫高濕下的接著性會提高,玻璃基 板與黏著劑層之間發生浮起或剝離之可能性有降低之傾 亚且,重加工性有提高之傾向,故較佳。另外,此重 ^平均分子量在2’_’⑻Q以下時’在其黏著劑層貼合之 光學膜之尺寸即使有所變化,也尺,㈣、σ 也因其尺寸變化會追隨著黏 :劑層:變動,故液晶單元之周圍部分㈣ 傾向,故較佳。重量平均分子量(Mw)與數平均分 子里(Μη)之比(Mw/Mn)所表示之分子量分布,通 10左右之範圍。 主 此丙烯酸系樹脂可僅由上述之較高分子吾者所、 亦可由該丙浠酸系樹脂以及與其相異之丙稀ς系樹脂的混 320560 15 200920811 合物所構成。作為混合後可使用之丙烯酸系樹脂,例如, γ列舉如:以源自前述式(1)所示之(甲基)丙烯酸酯之結構 單元作為主成分,且重量平均分子量為5〇,〇〇〇至3〇〇,〇〇〇 之範圍者。 丙烯酸系樹脂(組合2種類以上時是指兩者之混合. 物)’係將其溶解到乙酸乙酯中而調整成不揮發分濃度為 20重量%之溶液’在25。〇中以顯示2〇 · s以下(更佳為 〇士1至7^· s)之黏度為佳。此時之黏度在2〇pa· s以下 日守在同/皿同濕下之接著性會提高,玻璃基板與黏著劑層 之間發生浮起或剝離之可能性有侔低之傾向,並且,重加 工性有提高之傾向,故較佳。黏度係可藉由㈣从邮黏 度計來測定。 '構成黏著劑層之丙烯酸系樹脂,例如,可藉由溶㈣ 合法、乳化聚合法 ' 塊狀聚合法、懸濁聚合法等習知的各 種方法來製造。在製造此丙烯㈣、樹料,通常,係使用 聚合起始劑。聚合起始劑在製造丙料系樹脂時,相對於 所使用之全部單體的合計剛重量份,係使用㈣以$ 重量份左古。 • - . . · . 聚合起始劑係使賴聚合祕劑或光聚合起始劑等。 先聚合起始劑可列舉如:4♦經基乙氧基)苯基(2_經基 丙基)酮等。熱聚合起始劑可列舉如:如2,2,_偶氮雙里丁 腈(2,2-aZQbisisC)butyr()nitrile)、2,2,^^(2_m)、 u’-偶氮雙(環己燒+腈)、2,2,偶氮雙(2,4-二曱基戊猜 W偶氮雙(2,4-二甲基_4_甲氧基戊腈)、二甲基_2,2,_偶氮 320560 16 200920811 .雙(2-甲基丙酸醋)、2,2、偶氮雙(2_經 .化合物;如過氧化十二㈣、氫過^二1)等偶氮系 碳酸二異两酯、過苯、過氧二 有rm^fc(3’5,5_三甲基己醒基)等 男機過乳化物;如過石*鹼為 土’哥 、 過瓜馱鉀、過硫酸銨、過氧介药堂么η 過:化物等。同時,併用過氧化物 :還原、 ,〇Χ)系起始劑等,也可作為聚合起始劑使用遇原 作為丙婦酸系樹脂之製造方法,在上述所示方The energy base can be separately tested and can also be used as a material; the plural number I ~ medium, preferably the hydroxy group alone, the acid tree (10)) containing the polar official A is used as the composition of the C* ancient ~ Ganzi Another note is one of the early bodies of this base. At the same time, in addition to the early body of the base, it is also effective to use other single substances such as free "monomer". The weight of the base (for example, propylene + VIII volatiles used in the adhesive layer), the former, the resin (4)' relative to the structural unit, 甬2 is derived from the formula (1) The ratio of (meth) acrylate by weight) is m weight! Injury (preferably 80 to 99.6 structural units are usually contained in a ratio of 0" to 2 〇 旦 二 & 生 生 生 生 生 基 基). The inner resin (preferably 〇.4 to weight 320560 12 200920811) The acrylic resin (A) used in the present invention may also contain a (meth) acrylate derived from the above formula (1) and having a polar functional group. The structural unit of the monomer of the monomer is exemplified as, for example, a structural unit derived from a ($) acrylate having a lipid raft structure in a knives, and a benzene monomer alone. The structural unit, the structural saponin derived from a vinyl monomer, or a cyclized structure derived from a plurality of (meth) cyanofluorene-based structural units in a molecule, usually have a carbon number The structure of eyel Gparaffin of 5 or more (preferably about $7). Specific examples of the acrylate having an alicyclic structure include, for example, acetoacetate and propylene glycol hexanoate. Propylene propylene I — decyl pentoxide, cyclododecanyl acrylate v methacrylate hexyl acrylate, trimethylcyclohexyl acrylate, t-butylcyclohexyl acrylate, cyclohexyl ethoxy acrylate, cyclohexyl acrylate Specific examples of methacrylate, etc., having an alicyclic structure, such as phenyl ester, For example, methacrylic acid; borneol ester, cyclohexyl methacrylate, dicyclopentan vinegar methacrylate, methacrylic acid ring decocted vinegar, methyl methacrylate meth], methacryl oxime ^ Methylcyclohexyl vinegar, butyl butyl hexamethacrylate methacrylate, methacrylic acid hexyl benzene styrene, etc. As an example of the styrene monomer, in addition to styrene, Methylstyrene, dimethyl styrene, trimethylstyrene, ethyl styrene, diethyl styrene, triethyl styrene, propyl styrene, styrene, hexyl styrene, g Styrene, octyl phenethyl hydrazine, etc., styrene styrene fluorinated styrene, chlorinated styrene, styrene bromide, bismuth, stinky styrene, hardened styrene, etc. For example, nitrophenylethyl 320560 13 200920811 • olefin, ethoxylated styrene, methoxy styrene, divinyl benzene, etc. • Examples of ethylene-based monomers can be listed, such as vinyl acetate, C Acid B. ene s 曰, vinyl butyrate, vinyl 2-ethylhexanoate, vinyl dodecanoate, etc. g, such as gasification of ethylene (10) he or desertification ethylene special halogenated ethylene, such as vinylidene (vinyiene chi〇ride) and other vinylidene halides, such as vinyl pyridine, vinyl pyrrolidone, ethenyl hydrazine A nitrogen-containing monovalent ethylene group such as azole; a mono-olefin monomer such as butadiene, isoprene, and pentylene chloride; and examples thereof include acrylonitrile and methacrylonitrile. Examples of the monomer having a plurality of (meth)acryl fluorenyl groups in the molecule include, for example, 1,4-butanediol di(meth)acrylate, diacetic acid vinegar...diol di(methyl) Acetate vinegar 'Ethylene== propylene H-ethylene glycol di(meth)acrylic acid vinegar, tetraethylene acrylate, tripropylene glycol wing, product κ * 哔一π丞) __基之二西In the case of octamethylpropane tris(methyl)propionate, there are three (meth) acrylonitrile groups in the knives. '(M)-acrylic acid vinegar and monomer with polar functional group ^ ^ ^ 5 ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ a soil m) and a monomer other than a monomer having a polar functional group, for the non-volatile portion of the bribe, θ = 20 to 2 parts by weight (preferably 0 to ". by weight) The structural unit containing a ratio of a propyl acrylate is a main component, and the (3) is a block structure derived from a monomer having a polar functional group: 3 or more are contained in two or more. It is a kind of propylene glycol resin. 320560 14 200920811 'In addition, in the acrylic resin, it is also possible to mix C: an olefinic wax (specifically, for example, a structural soap derived from the (meth) acrylate of the formula (1)) And (4) acid tree material which does not contain a polar functional group). The acrylic resin derived from the structural unit derived from the (mercapto)propionic acid vinegar of the formula (1) as a main component and containing a structural unit derived from a monomer having a polar functional group is used in the entire acrylic resin. In the case of 60% by weight or more, more preferably 8% by weight or more. (4) Acrylic resin containing structural units of (meth)acrylic acid g (4) as a main component and containing (iv) a structural unit derived from a monomer having a polar uterine group, by gel permeation chromatography The weight average molecular weight (Mw) of the (GPC) method converted into the standard polystyrene is preferably in the range of (4). When the weight average molecular weight converted to standard polystyrene is 1'0:0,000 or more, the adhesion under high temperature and high humidity is increased, and the possibility of floating or peeling between the glass substrate and the adhesive layer is lowered. Yahe, the reworkability tends to increase, so it is preferred. In addition, when the weight average molecular weight is 2'_'(8)Q or less, the size of the optical film bonded to the adhesive layer may be changed even if it is changed, and (4) and σ may follow the viscosity due to the dimensional change. The layer: varies, so the surrounding portion (4) of the liquid crystal cell tends to be preferable. The molecular weight distribution represented by the ratio (Mw/Mn) of the weight average molecular weight (Mw) to the number average molecular (Mw/Mn) is in the range of about 10 or so. Mainly, the acrylic resin may be composed of only the above-mentioned higher molecular weight, or a mixture of the acrylic acid-based resin and the acrylonitrile-based resin different therefrom, 320560 15 200920811. As the acrylic resin which can be used after the mixing, for example, γ is exemplified by a structural unit derived from the (meth) acrylate represented by the above formula (1) as a main component, and the weight average molecular weight is 5 Å, 〇〇 〇 to 3〇〇, the scope of the 。. The acrylic resin (in the case of a combination of two or more types, a mixture of the two) was prepared by dissolving it in ethyl acetate and adjusting it to a solution having a nonvolatile concentration of 20% by weight. It is better to display the viscosity of 2 〇 · s or less (more preferably gentleman 1 to 7^· s). When the viscosity at this time is 2 〇pa·s or less, the adhesion between the glass substrate and the adhesive layer is increased, and the possibility of floating or peeling between the glass substrate and the adhesive layer tends to be low, and The reworkability tends to be improved, so it is preferred. Viscosity can be determined by (4) from a viscous meter. The acrylic resin constituting the pressure-sensitive adhesive layer can be produced, for example, by various methods known in the art of "solution", emulsion polymerization, bulk polymerization or suspension polymerization. In the production of the propylene (tetra), tree material, usually, a polymerization initiator is used. When the polymerization initiator is used to produce a propylene-based resin, it is used in a (fourth) basis by weight of the total weight of the total monomers used. • - . . . . The polymerization initiator is a photopolymerization initiator or a photopolymerization initiator. The polymerization initiator can be exemplified by, for example, 4 ♦ benzyloxy)phenyl (2-propylpropyl) ketone and the like. The thermal polymerization initiator may be, for example, 2,2,-azobisnityronitrile (2,2-aZQbisisC) butyr () nitrile), 2, 2, ^^ (2_m), u'-azo double (cyclohexane + nitrile), 2, 2, azobis (2,4-didecylpentanyl bis(2,4-dimethyl-4-methylpentyl valeronitrile), dimethyl _2, 2, _ azo 320560 16 200920811 . bis (2-methylpropionic acid vinegar), 2, 2, azobis (2_ by. compound; such as 12 (tetra) peroxide, hydrogen ^ 2) Such as azo diisocarbamate, benzene, peroxygen rm^fc (3'5,5_trimethylhexyl) and other male machine over-emulsified; such as stone * alkali for soil ' brother , 驮 驮 驮 potassium, ammonium persulfate, peroxy pharmaceutics η :: compound, etc. At the same time, the use of peroxide: reduction, 〇Χ) initiator, etc., can also be used as a polymerization initiator Originally used as a method for producing a propylene glycol resin, in the above-mentioned manner

法較佳。在列舉溶液聚合法之具體例而說明 Γ可例舉:將㈣望之單體及有機㈣混合,於氮I 合起始劑,在4。至町右,較= C左讀拌3至1〇小時左右之方法等。 ;制=’在單體或熱聚合起始劑聚合中連續或間歇:; 口古2亦可以溶解於有機溶劑中之狀態來添加。在此,作 如可使用例如:甲苯、二甲苯等芳香族烴類八 乙酸谓等賴;丙醇、異丙基醇等脂肪族 雜。丙㉟、甲基乙基_、甲基異丁基·等嶋等。 [離子性化合物(Β)] • - · 头」在本發明中,除了如以上之丙烯酸系樹脂(Α)之外,作 几靜電劑者是使用在室溫(25。〇中為固體的離子性化合 务⑻。此離子性化合物⑻係具有有機陽離子。該在室: :==離子性化合物’在本說时中,有時㈣為 320560 17 200920811 ,構成離子性化合物(B)之 為離子性固體之條件的 :可只==足會 朗離子、鑽陽離子”比唆鐵陽離子、 _使用時’從將在其上設置的剝離膜^^之黏著劑層 之觀點而言,以吡啶鑌胃’、以剝離時不易帶電 其.士 疋“離子、及咪唑鑌陽離子為佳。 力一方面’在離子性化合物 分的相對離子的陰離子成分, ,、、、14陽離子成 體之條件者即可,而益特別㈣足成為離子性固 可A^ ”別限疋可為無機之陰離子,也 為有機之陰離子,例如可列舉如下述者。 氯化物陰離子[cr]、 溴化物陰離子[Br-]、 蛾化物陰離子[厂]、 '四氯鋁酸鹽陰離子[A1C14—]、 七氯二鋁酸鹽陰離子[A12C17_]、 四氟硼酸鹽陰離子[BF4_]、 5氟磷酸鹽陰離子[PF6-]、j 全氯酸鹽陰離子[Cl〇4_]、 — 硝酸鹽陰離子[no3—]、 乙酸酯陰離子[ch3coct]、 三氟化乙酸酯陰離子[cf3coo—]、 甲磺酸鹽陰離子[CH3S〇r]、 三氟曱磽酸鹽陰離子[cf3so3—]、 對甲苯磺酸鹽陰離子[p_CH3C6H4S〇3-j、 320560 18 200920811 雙(三氟甲磺醯基)醯亞胺陰離子[(cf3so2)2n-]、 蒼(二氟甲磺酿基)甲基體陰離子[(CF3S02)3C_]、 六氟砷酸鹽陰離子[AsF6-]、 六氟録酸鹽陰離子[SbF6-]、 六氟銳酸鹽陰離子[NbF6—]、 六氟组酸鹽陰離子[Ta]p6-]、 二甲基次亞磷酸鹽陰離子[(Ch3)2p〇〇-]、 (聚)氫氟氟化物陰離子[F(HF)ir](n是i至3左右)、 二氰胺化物陰離子[(CN)2N—]、 硫氰化物陰離子[SCN—]、 全氟丁磺酸鹽陰離子[C4;p9S〇3-]、 雙(五氟乙磺醯基)醯亞胺陰離子[(C2F5S〇2)2N-]、 全氟丁酸酯陰離子[C3F7C〇〇-]、 (二氟甲續醯基)(三氟甲烷羰基)醯亞胺陰離子 [(CF3S02)(CF3C0)N]等。 其中,以含氟原子之陰離子成分係因賦予抗靜電性優 異之離子性固體,故為適合使用,尤其以六㈣酸鹽 (hexafluorophosphate)陰離子為佳。 •本發明所使用之離子性固體的具體例子, 撰煜 自上述陽離子成分與陰離子成分之組合。具體公;= 離子與陰離子成分之組合的化合物,可列舉如下述者。 /、鼠鱗酸N-己基π比σ定鏽鹽、 /、氟磷酸Ν-辛基η比σ定鑌鹽、 六氟磷酸Ν-丁基-4-甲基吡啶錯鹽、 320560 19 200920811 六氟磷酸N-丁基-N-曱基吡咯啶鏽鹽 /、鼠石粦酸1-乙基-3-曱基味π坐鑷鹽、 對曱苯磺酸1-乙基-3-甲基咪唑鏽鹽、 甲石黃酸1-丁基-3 -甲基味η坐鏽鹽、 六氟鱗酸四丁基銨鹽 對曱苯磺酸四丁基銨鹽、 二甲基磷酸(2-羥基乙基)三曱基銨鹽等。 如此之離子性固體是可各別單獨使用,亦 ^來使用。離子性固體之例子,並不限定上述列::: 在室溫中為固體之離子性化合物⑻是如前述,在由> 酸賴脂(Α)之組絲所形叙料制巾,不^ ^几靜電性’同時可有效地保有作為黏著劑之諸物性。-尤 使用在常溫下為液體之離子性化合物之情形相比, 能。從如此之抗靜電性的長期安定 3威點而0,離子性化合物⑻是以具有3 0。(:以上(最好 二厂C,上)之溶點為佳。另一方面’其溶點太高時,因 。〜、、丙婦酸系樹月旨⑷之相溶性會變I,所以以具有在9〇 C以下(較佳為在8〇〇c以下)之熔點更佳。 離子性化合物⑻,相對於前述之丙婦酸系樹脂(A)的 ^軍么刀100重置份(使用2種以上時為其合計重量),係 j 0.2至8重i份之比率含有。相對於前述之丙烯酸系樹 =)的不揮發分ϊ〇〇重量份,離子性化合物⑻含有〇 2 里伤以上知,因抗靜電性能會提高故較佳,另外,其量 320560 20 200920811 • LIT!以下時,因容易保有耐久性故較佳。相對於前 •述之丙烯馱系樹脂(A)的不揮發分1〇〇重量份,離子 •物(B)之置可為0·2至5重量份之範圍,較佳是在ο;重曰 份以上且在3重量份以下。 1 [構成黏著劑之其他成分] 、,在以上之丙烯酸系樹脂(Α)及離子性化合物(Β)中,通 f是再調配交聯劑(C),來作為黏著劑組成物。交聯劍二 /疋在刀子内至少具有2個官能基之化合物,該官能基可盘 丙烯酸系樹脂⑷中特別是源自含有極性官能基之單體的、 .結構單元進行交聯,交聯劑(C)具體上可例示如:異氰酸酯 系化合物、環氧系化合物、金屬螯合系化合物、氮雜環丙 烷(aziridiiie)系化合物等。 ' ( 異氰酸醋系化合物係在分子内至少具有2個異氯酸其 (isocyanato ; -NCO)的化人物,例如•妯田— 土 σ物,例如.伸甲苯二異氰酸酯、 六亞甲基二異氰酸酯、異佛爾酮二異氰酸酯、伸二甲苯二 1,異氰酸酯、加氫伸二甲苯二異氰酸酯、二苯基曱烷二異^ 酸醋、加氫二苯基m氰酸醋、蔡二拜氛酸酉旨、^苯- 甲烧三異氰酸酯等。同時’在此等異氰酸醋化合物中,使 甘油或三經甲基丙燒等多醇反應後所得之加成物、或使里 氰酸醋化合物作成二量體、三量體等者,亦可作為在黏著 劑中使用的交聯劑。亦可以將2種以上之異氰酸_系化合 _物混合後使用。 環氧系化合物係在分子内至少具有2個環氧基之化合 物,例如,可列舉:雙紛A型之環氧樹脂、乙二醇二縮水 320560 21 200920811 甘油醚、聚乙二醇二縮水甘油醚、甘油二縮水甘油醚、甘 油三縮水甘油醚、1,6-己二醇二縮水甘油醚、三羥甲基丙 烷三縮水甘油醚、N,N-二縮水甘油基苯胺、N,N,N,,N、四 縮水甘油基間-二甲苯二胺、,一二縮水甘油胺 基甲基)環己烷等。亦可以將2種以上之環氧系化合物混合 後使用。 作為金屬螯合化合物者,例如,可列舉:對於紹、鐵、 銅、鋅、錫、鈦、鎳、銻、鎂、釩、鉻及鍅等多價金屬, 使乙酿丙嗣或乙酸乙酸乙酯配位而成之化合物等。 氮雜環丙烷(aziridine)系化合物是在分子内至少具有 2個亦稱為伸乙基亞胺(ethyiene imjne)之由1個氮原子與2 個碳原子所成之3員環骨幹的化合物,可列舉如:二苯基 曱烷-4,4、雙(1-氮雜環丙烷甲醯胺)、甲苯_2,4_雙(1_氮雜環 丙烷甲醯胺)、三伸乙基三聚氰胺(triethylenemelamine)、 異鄰苯二甲醯基雙甲基氮雜環丙烷)、氧化參氮雜 環丙羞膦、六亞甲基-1,6-雙(1_氮雜環丙烷甲醯胺)、三經 甲基丙烧-二-/5 _-氮雜ί哀丙基丙酸醋,、四經甲基曱烧三·沒_ 氮雜環丙基丙酸酯等。 此等交聯劑中,較適用者為:異氰酸醋系化合物、尤 其疋伸二曱苯二異氰酸酯、伸甲苯二異氰酸酯或是六亞甲 基二異氰酸酯;或由使此等異氰酸醋化合物與甘油或三羥 甲基丙烷4多元醇反應而得之加成物;或使異氰酸酯化合 物成為二量體、三量體等者之混合物;或將此等異氰酸酯 系化合物經混合而成者等。作為適合之異氰酸酯系化合物 22 320560 200920811 者,可列舉如:伸曱苯二異氰酸酯、使伸曱苯二異氰酸酯 -與多醇反應而得之加成物、伸曱苯二異氰酸酯之二量體、 .及伸甲苯二異氰酸酯之三量體、或六亞曱基二異氰酸酯、 使六亞甲基二異氰酸酯與多元醇反應而得之加成物、六亞 甲基二異氰酸酯之二量體、及六亞曱基二異氰酸酯之三量 體等。 關於交聯劑(C),相對於丙烯酸系樹脂(A) 100重量份 (使用2種類以上時是其合計重量),通常是以〇 〇 1至j 〇 重量份’較佳為0.1至5重量份左右之比率來調配。相對 於丙烯酸系樹脂(A) 100重量份,交聯劑(〇的量為〇.〇】重 量份以上時’因黏著劑層之耐久性有提高之傾向,故較佳, 另外,在10重量份以下時,因附黏著劑之光學膜在使用於 液晶顯不裝置時的白點狀缺色會變成不顯著,故較佳。 本發明之附黏著劑之樹脂膜,在以其黏著劑層側貼合 於玻璃基板時,在用以形成該黏著劑層之黏著劑上,為了 要提高黏著劑層與玻璃基板之密著性,以含有料系化合 物為佳’尤其是以使在調配交聯劑前的丙烯酸系樹脂中含 有矽烷系化合物為更佳。 雜系化合物之例子,可縣如:乙烯基三甲氧基^ 烷、乙晞基二乙氧基石夕院、乙烯基參(2'甲氧基乙氧基)夺 燒、N-(2-胺基乙基)_3_胺基丙基甲基二甲氧基石夕燒、^ ( 胺基乙基)·3·胺基丙基三甲氧基錢、3·胺基丙基三乙氧 =二甘:氧基丙基三甲氧基梦烧、3_縮水甘油孽 土 土土 —甲氧基矽燒、2-(3,4-環氧環己基)乙基三甲』 320560 23 200920811 基矽烷、3-氯化丙基曱基二曱氧基矽烷、3-氯化丙基三曱 氧基矽烷、3-甲基丙烯醯氧基丙基三甲氧基矽烷、3-氫硫 基丙基三甲氧基矽烷、3-縮水甘油氧基丙基三乙氧基矽 烧、3 -縮水甘油氧基丙基二曱氧基曱基石夕烧、3 -縮水甘油 氧基丙基乙氧基二甲基矽烷等。亦可使用2種類以上之石夕 烧系化合物。 石夕烧系化合物亦可為聚^夕氧寡合物(silicone oligomer) 型者。將聚矽氧寡合物以(單體)寡聚合物之形式表示時, 例如,可列舉如下述者。 如3-氮硫基丙基三曱氧基發烧-四甲氧基碎烧共聚合物、 3-氫硫基丙基三曱氧基矽烷-四乙氧基矽烷共聚合物、 3-氫硫基丙基三乙氧基矽烷-四曱氧基矽烷共聚合物、 3-氫硫基丙基三乙氧基矽烷-四乙氧基矽烷共聚合物等 含有氫硫基丙基的共聚合物;如 氳硫基曱基三曱氧基矽烷-四曱氧基矽烷共聚合物、 氳硫基曱基三曱氧基矽烷-四乙氧基矽烷共聚合物、 氫硫基曱基三乙氧基矽烷-四甲氧基矽烷共聚合物、 氫硫基曱基三乙氧基矽烷-四乙氧基矽烷共聚合物等含 有氫硫基甲基的共聚合物;如. 3-曱基丙烯醯氧基丙基三曱氧基矽烧-四曱氧基矽烷共 聚合物、 3-曱基丙烯醯氧基丙基三甲氧基矽烷-四乙氧基矽烷共 聚合物、 3-甲基丙烯醯氧基丙基三乙氧基矽烷-四曱氧基矽烷共 24 320560 200920811 聚合物、 ' 3-甲基丙烯醯氧基丙基三乙氧基矽烷-四乙氧基矽烷共 ,聚合物、 3-曱基丙烯醯氧基丙基曱基二甲氧基矽烷-四甲氧基矽 烧共聚合物、 3-曱基丙烯醯氧基丙基曱基二曱氧基矽烷-四乙氧基矽 烧共聚合物、 3-甲基丙烯醯氧基丙基甲基二乙氧基矽烷-四甲氧基矽 烧共聚合物、 3-甲基丙烯醯氧基丙基甲基二乙氧基矽烷-四乙氧基矽 烷共聚合物等含有甲基丙烯醯氧基丙基的共聚合物;如 3-丙烯醯氧基丙基三甲氧基矽烷-四曱氧基矽烷共聚合 物、: 3-丙烯醯氧基丙基三曱氧基矽烷-四乙氧基矽烧共聚合 物、 3-丙烯醯氧基丙基三乙氧基矽烷-四曱氧基矽烷共聚合 物、 3-丙烯醯氧基丙基三乙氧基矽烷-四乙氧基矽烷共聚合 物、 3-丙烯醯氧基丙基曱基二甲氧基矽烷-四曱氧基矽烷共 聚合物、 3-丙烯醯氧基丙基甲基二甲氧基矽烷-四乙氧基矽烷共 聚合物、 3-丙烯醯氧基丙基甲基二乙氧基矽烷-四曱氧基矽烷共 25 320560 200920811 聚合物、 3-丙烯醯氧基丙基甲基二乙氧基矽烷-四乙氧基矽烷共 聚合物等含有丙烯醯氧基丙基的共聚合物;如 乙烯基三甲氧基矽烷-四曱氧基矽烷共聚合物、 +乙炸基二甲氧基碎院-四乙氧基碎烧共聚合物、 乙烯基三乙氧基矽烷-四甲氧基矽烷共聚合物、 乙烯基三乙氧基矽烷-四乙氧基矽烷共聚合物、 乙烯基曱基二甲氧基矽烷-四曱氧基矽烷共聚合物、 乙烯基曱基二甲氧基矽烷-四乙氧基矽烷共聚合物、 乙烯基曱基二乙氧基矽烷-四曱氧基矽烷共聚合物、 乙烯基曱基二乙氧基矽烷-四乙氧基石夕烷共聚合物等含 有乙稀基的共聚合物;如 3-胺基丙基三曱氧基矽烷-四曱氧基矽烷共聚合物、 3-胺基丙基三曱氧基矽烷-四乙氧基矽烷共聚合物、 3-胺基氧丙基三乙氧基矽烷-四甲氧基矽烷共聚合物、 3-胺基丙基三乙氧基矽烷-四乙氧基矽烷共聚合物、 3-胺基丙基曱基二甲氧基矽烷-四曱氧基矽烷共聚合物、 3-胺基丙基甲基二甲氧基矽烷-四乙氧基矽烧共聚合物、 3-胺基丙基曱基二乙氧基矽烷-四曱氧基矽烷共聚合物、 3 -胺基.丙基曱基二乙氧基梦烧四乙氧基砍烧共聚合物 等含有胺基的共聚合物等; 此等矽烷系化合物,大多是液體。在黏著劑中之矽烷 系化合物之調配量,相對於丙稀酸系樹脂(A)之不揮發分 100重量份(使用2種類以上時是其合計重量),通常是以 26 320560 200920811 0.01至10重量份左右,較佳為以使用0.05至5重量份左 右之比率使用。相對於丙烯酸系樹脂之不揮發分丨〇〇重量 份’石夕烧系化合物之量為0.01重量份以上時,因黏著劑層 與玻璃基板之密著性會提高,故較佳。另外,其量在10 重量份以下時,因有可抑制矽烷系化合物從黏著劑層流出 之傾向,故較佳。 在以上說明之黏著劑中,亦可再調配交聯觸媒、耐候 安定劑、增黏劑、可塑劑、軟化劑、染料、顏料、無機填 充劑、丙烯酸系樹脂(A)以外之樹脂等。另外,在黏著劑^ 調配紫外線硬化性化合物,於形成黏著劑層後照射紫外線 而使其硬化,可成為較硬之黏著劑層。其中,在黏著劑中 若同時調配交聯劑與交聯觸媒,則可藉由短時間内之熟成 而調製黏㈣層’在所得之附黏著劑之樹脂财,可抑制 在樹脂膜與黏著劑層之間所發生之浮起或剝離的現象、在 =劑層_產生之起泡’並且,重加工性也變成更為良 好。作為交聯觸媒者,可以列舉如:六亞甲.基二胺乙 f:胺、聚伸乙基亞胺、六亞甲基四胺、二伸乙基三胺、 ί甲胺:異佛爾酮二胺、三亞甲基二胺、聚胺基樹 交聯觸媒之胺系化合著劑中調配料 宜。 ^又聯财以異氰酸酯系化合物為 構成黏著劑之此等各虚公 w 為黏著劑組成物,在適♦之二广解到溶劑中之狀態成 黏著劑層。 田之基材上塗布,經乾燥後就成為 320560 27 200920811 本發明之附黏著劑之樹脂膜中十 脒八產β $ 〇。I 犋中黏者劑層是以使其凝 膠刀率成為50至99重量%之範圍之方式 凝膠分率係依以下之(I)至(IV)所測得之值。、’’、、且 , 將約8㈣約8em之面積之黏著劑層,與由約心 ⑽之SU讓所成之金屬網(其重量當作勤)貼合。 =秤得上述⑴:得之貼合物的重量,其重量當作I其 -人,以包圍住黏者劑層之方式折疊 田—^ 且4-人亚以釘書釘(Stapler) 固疋住之後,秤重,其重量當作Wb。 =)在玻璃容器中放人上述(11)以釘“ i^住之網狀 ::力:入60 W乙酸乙酯並予以浸潰後,將 室溫中保管3天。 ^ (IV)自破璃容器取出網狀物,於12旳乾燥μ小時後,秤 重,其重量當作Wa,依據下式計算凝膠分率。 ’凝膠分袍量 %MiWa_(Wb_Ws)_Wm}/(Ws_Wm)]测 黏著劑層之凝膝分率在5G.重量%以上時,因黏著劑層 之,久性有提高傾向’故較佳’另外’其凝膠分率在的 重量%以下時,因容易製造,故較佳。 右要將黏著劑層之凝膠分率調整到5〇至99重量.%, ,雖^依屬於黏著劑層之有效⑨分的丙稀酸系樹脂之種 f不同而異’但只要增.加交聯劑之量,就會使凝膠分率變 二’故Η依據交聯劑之量而調整凝膠分率為宜。具體而 θ才對於構成黏著劑層之丙烯酸系樹脂的不揮發分1 〇〇 重^份(使用2種類以上時為其合計量),交聯劑之調配量 二要在0.〇1至1 〇重量份左右之範圍中,配合丙烯酸系 320560 28 200920811 .樹脂t種類而適#選擇即可。黏著劑層之凝膠分率係以在 』6重里/〇乂上(在75重置〇/〇以上較佳)且在95重量%以 佳。 门 [附黏著劑之樹脂膜] 本發明之附黏著劑之樹脂膜,係在樹脂膜的至少一方 的面上,設置有由以上的黏著劑組成物所形成的黏著劑層 者。在此’所使用之樹脂膜係可例舉如:包含選自偏光膜 及相位差膜之膜的来墨腾·.斗 尤予臊,或貼合在作為被保護體之光學 膜等上,以保護其表面免於損傷或污染等之目的而使用的 表面保護膜等。 偏光膜係指相對於自然光等入射光,具有射出偏光之 機能的光學膜。偏光膜中有下述數種類型:吸收呈有某方 向之振動面的直線料,並具備使具有與其呈垂直之振動 面的直線偏光穿透之性質的直線偏光膜;反射具有某方向 之振動面的直線偏光,並具備使具有與其呈垂直之振動面 的直線偏光穿透之性質的偏光分離膜;由偏光膜與後述之 相位差膜所積層成的擴圓偏光膜等。偏光膜,尤其是直線. 偏光膜(可稱為偏光片,亦或稱為偏光片膜)之適當具體 例,可列舉如:在一轴延伸之聚乙稀醇系樹脂膜中,吸附 配向有碘或二色性染料等二色性色素者。 相位差膜是指顯示光學異向性的光學膜,可列舉如: 將由聚乙烯醇、聚碳酸醋、聚酯、聚丙烯酸酉旨、聚醯亞胺、 聚稀煙、環狀聚烯烴、聚苯乙稀、聚礙(polysulW)、聚 _硬I偏一敦乙烯/聚甲基丙稀酸甲醋、液晶聚醋、乙酸 320560 29 200920811 纖維素、乙烯-乙酸乙烯酯共聚合物皂化物、聚氣化乙烯等 所成之高分子膜予以延伸101至6倍左右而得之延伸膜 .等。其中,以將聚碳酸酯膜或環狀聚烯烴系膜予以一軸延 伸或二軸延伸而得之高分子膜較佳。一軸性相位差膜雖也 有稱為廣視野角相位差膜、低光彈性率相位差膜等,但對 任何一種皆可適合使用。 另外,藉由液晶性化合物之塗布、配向而表現光學異 向!·生之膜,或藉由無機層狀化合物之塗布而表現光學異向 性之膜’都可以作為相位差膜使用。如此之相位差膜ψ, 也有稱為溫度補償型相位差膜者,另外,有例如新日本石 油公司以「LC膜」之商品名所販售的由棒狀液晶經扭轉配 向而成之膜、同樣的新日本石油公司以「簡膜」之商品 名戶^販售的由棒狀液晶經傾斜配向而成之膜、富士膜公司 X WV膜」之商品名所販㈣由圓盤狀液晶經傾斜配 :=、住友化學公司,「VAC膜」之商品名所販售的 轴配向型之膜、同樣的住友化學公司以「新VAC膜」 之商品名所販售的二軸配向型之膜等。 、」 作光:Ϊ使:在此等光學膜上貼著保護膜而成者,亦可會 例如二Γ以,護膜是使用透明之樹脂膜,此透明樹腊 ,纖維素系樹脂、以聚曱基丙婦酸甲g旨所乙 酉夂系树脂、聚酯樹脂、聚烯烴樹 “ _樹脂、聚_赌等。在構成保護膜 杨义§日糸化合物、二苯甲酮系化合物、苯并三唾系价 320560 30 200920811 • 口/二并系化合物、氰基丙烯酸酯系化合物、鋅妒入私 .鹽系化合物”外、㈣㈣。保護膜細 .素膜等乙醯纖維系樹脂膜為宜。 一乙fe纖維 在上述之光學膜中,直線偏光膜係多半廿 之偏光片(例如由聚乙烯醇系樹脂所成 κ 八 或雙面上貼莫古位# / 烏先片膜)的單面 或又面上貼者有保護膜之狀態來使用。另外 偏光膜雖然係由直線偏光膜與相位差膜所積 = 二也多:為在偏光片膜的單面或雙面上貼著有保護膜: “。在,此之橢圓偏光膜上’依本發明而形成黏著劑層 日守,通常是在其相位差膜侧形成黏著劑層。 表面保護膜是指為了保護作為被保護體之光學膜等免 於表面損傷或污染之目的而使用的膜,例如,在液晶顯示 I置的生產中所使用之偏光膜、相位差膜、光擴散薄片、 反射薄片等各種光學膜,係以在其表面(當單面具有黏著劑 層時,是指與此黏著劑層為相反側的面)貼合有表面保護膜 的狀態來流通,並在貼合於液晶單元等之後,通常是剝‘ 除去該表面保護膜。表面保護膜之基材,例如可列舉:如 聚乙烯、聚丙:/#'聚曱基戊烤等聚稀煙系樹脂;如聚氣化 乙缚、χκ偏一氟i乙烯、聚二氟乙烧(p〇lyethyleneflu〇Tide) 等氟化聚烯烴系樹脂;如聚萘二曱酸乙二酯(p〇lyethylene Naphthalate)、聚對笨二曱酸乙二酯(p〇lyethyleneThe method is better. A specific example of the solution polymerization method will be described. Γ Γ : : : : 混合 混合 混合 单体 单体 单体 单体 单体 单体 单体 单体 单体 单体 单体 单体 单体 单体 单体 单体 单体 单体 单体 单体 单体 单体 单体 单体 单体To the right of the town, compare = C left to mix for 3 to 1 hour or so. ; system = 'continuous or intermittent in the polymerization of the monomer or thermal polymerization initiator:; the mouth 2 can also be added in a state of being dissolved in an organic solvent. Here, for example, an aromatic hydrocarbon octaacetic acid such as toluene or xylene may be used, and an aliphatic compound such as propanol or isopropyl alcohol may be used. C35, methylethyl_, methyl isobutyl, etc. [Ionic compound (Β)] • - · Head" In the present invention, in addition to the above acrylic resin (Α), a few electrostatic agents are used at room temperature (25. Sexualization (8). The ionic compound (8) has an organic cation. The in-situ: :== ionic compound 'in this case, sometimes (d) 320560 17 200920811, constituting the ionic compound (B) as an ion Conditions of a solid solid: only == foot chelating ion, drilling cation "thanth bismuth iron cation, _ when used" from the viewpoint of the adhesive layer of the release film to be disposed thereon, pyridinium The stomach 'is not easy to be charged when peeling off. The sputum "ion, and imidazolium cations are preferred. On the one hand, the ionic component of the relative ion of the ionic compound, the condition of the cation, However, the specific (4) foot becomes an ionic solid A^", and may be an inorganic anion or an organic anion, and examples thereof include the following: chloride anion [cr], bromide anion [Br- ], moth compound anion [factory], 'tetrachloroaluminate anion [A1C14—], heptachlorodisuccinate anion [A12C17_], tetrafluoroborate anion [BF4_], 5 fluorophosphate anion [PF6-], j perchlorate anion [Cl 〇4_], — nitrate anion [no3—], acetate anion [ch3coct], trifluorinated acetate anion [cf3coo—], mesylate anion [CH3S〇r], trifluoroantimonate Anion [cf3so3—], p-toluenesulfonate anion [p_CH3C6H4S〇3-j, 320560 18 200920811 bis(trifluoromethanesulfonyl) quinone imine [(cf3so2)2n-], Cang (difluoromethane Methyl anion [(CF3S02)3C_], hexafluoroarsenate anion [AsF6-], hexafluoroate anion [SbF6-], hexafluoroate anion [NbF6-], hexafluoroacid Salt anion [Ta]p6-], dimethyl hypophosphite anion [(Ch3)2p〇〇-], (poly) hydrofluorofluoride anion [F(HF)ir] (n is about i to 3) , dicyandiamide anion [(CN)2N-], thiocyanide anion [SCN-], perfluorobutanesulfonate anion [C4; p9S〇3-], bis(pentafluoroethanesulfonyl)pyrene Amine anion [(C2F5S〇2)2N-], Fluorobutyrate anion [C3F7C〇〇-], (difluoromethyl fluorenyl) (trifluoromethanecarbonyl) quinone imine anion [(CF3S02)(CF3C0)N], etc. Among them, an anion component of a fluorine atom It is suitable for use because it imparts an ionic solid excellent in antistatic property, and particularly preferably a hexafluorophosphate anion. A specific example of the ionic solid used in the present invention is composed of a combination of the above cationic component and anionic component. Specific examples of the compound of the combination of an ion and an anion component include the following. /, rat squaric acid N-hexyl π ratio σ rust salt, /, fluorophosphate Ν-octyl η ratio σ 镔 salt, hexafluorophosphate 丁基-butyl-4-methyl pyridine salt, 320560 19 200920811 six N-butyl-N-decylpyrrolidinium fluorophosphate rust salt, 1-ethyl-3-indolyl sulphonic acid sulphonic acid, 1-ethyl-3-methyl sulfonate Imidazole rust salt, 1-butyl-3-methyl sulphate, sulphate salt, tetrabutylammonium hexafluorophosphate, tetrabutylammonium sulfonate, dimethyl phosphate (2- Hydroxyethyl)trimethylammonium salt and the like. Such ionic solids can be used individually and separately. Examples of the ionic solids are not limited to the above columns:: The ionic compound (8) which is solid at room temperature is as described above, and is formed into a towel formed by the group of > acid lysine (Α), not ^^Several electrostaticity' can effectively retain the physical properties as an adhesive. - In particular, it can be used in the case of using an ionic compound which is liquid at normal temperature. From the long-term stability of such antistatic properties, the ionic compound (8) has 30. (: The melting point of the above (preferably the second plant C, the top) is better. On the other hand, when the melting point is too high, the compatibility of the ~, and the potassium ketone tree (4) will change to I, so It is more preferable to have a melting point of 9 〇C or less (preferably 8 〇〇c or less). The ionic compound (8) is a reset portion relative to the above-mentioned propylene glycol resin (A). When two or more types are used, the total weight thereof is contained in a ratio of 0.2 to 8 parts by weight, and the ionic compound (8) contains 〇2 of the non-volatile parts by weight of the acrylic tree as described above. In addition, it is preferable that the antistatic performance is improved, and the amount is 320560 20 200920811. When LIT is below, it is preferable because it is easy to maintain durability. The ion (B) may be in the range of from 0.2 to 5 parts by weight, preferably in the range of from 0 to 2 parts by weight based on 1 part by weight of the propylene-based resin (A). The amount is more than 3 parts by weight. 1 [Other components constituting the adhesive], in the above acrylic resin (Α) and ionic compound (Β), the crosslinking agent (C) is further formulated as an adhesive composition. Crosslinking Sword 2/疋 has at least two functional groups in the knives, and the functional group can be crosslinked and crosslinked by a structural unit derived from a monomer having a polar functional group, particularly a monomer having a polar functional group. Specific examples of the agent (C) include an isocyanate compound, an epoxy compound, a metal chelate compound, and an aziridiiie compound. ' (Isocyanic acid-based compound is a person having at least two isochloric acid (isocyanato; -NCO) in the molecule, for example, 妯田-土σ, for example, toluene diisocyanate, hexamethylene Diisocyanate, isophorone diisocyanate, xylene di 1, isocyanate, hydrogenated xylene diisocyanate, diphenyl decane diisoacetate, hydrogenated diphenyl m cyanate, Cai dibenzic acid酉, Benzene-Methyl triacetate, etc. At the same time, 'in these isocyanate vinegar compounds, the glycerin or the adduct obtained by reacting a polyhydric alcohol such as methyl propyl ketone or the cyanic acid vinegar The compound may be used as a dimer or a triad, or may be used as a crosslinking agent for an adhesive. It may be used by mixing two or more kinds of isocyanate compounds. The epoxy compound is used. A compound having at least two epoxy groups in the molecule, for example, an epoxy resin of a double type A, a dihydrate of ethylene glycol 320560 21 200920811 glyceryl ether, polyethylene glycol diglycidyl ether, glycerol diglycidyl Ether, glycerol triglycidyl ether, 1,6-hexanediol condensate Oleic ether, trimethylolpropane triglycidyl ether, N,N-diglycidylaniline, N,N,N,,N,tetraglycidyl meta-xylenediamine, diglycidylamine Methyl) cyclohexane or the like. Two or more epoxy compounds may be mixed and used. As the metal chelate compound, for example, a polyvalent metal such as sulphur, iron, copper, zinc, tin, titanium, nickel, lanthanum, magnesium, vanadium, chromium, and lanthanum may be used. A compound in which an ester is coordinated. An aziridine-based compound is a compound having at least two three-membered ring skeletons, which are also known as ethyiene imjne, having one nitrogen atom and two carbon atoms in the molecule. For example, diphenyldecane-4,4, bis(1-azetidinecarbamamine), toluene-2,4-bis(1-azacyclopropanecarbamamine), tri-ethylidene Triethylenemelamine, isophthalic acid bismethylaziridine), oxidized niobium sulfaphosphine, hexamethylene-1,6-bis(1-azacyclopropanecarbamide ), trimethyl ketone-di-/5 _-aza propyl propyl vinegar, tetramethyl sulfonate tris - no _ azacyclopropyl propionate and the like. Among these crosslinking agents, those suitable for use are: isocyanic acid-based compounds, especially bismuth diphenylene diisocyanate, toluene diisocyanate or hexamethylene diisocyanate; or by making such isocyanate compounds An adduct obtained by reacting with glycerin or trimethylolpropane 4 polyol; or a mixture of an isocyanate compound as a dimer or a triad or a mixture of these isocyanate compounds; Examples of suitable isocyanate-based compounds 22 320560 200920811 include diphenyl phthalocyanate, an adduct obtained by reacting phenylene diisocyanate with a polyhydric alcohol, and a dimer of phenylene diisocyanate. And a trimer of toluene diisocyanate or hexamethylene diisocyanate, an adduct obtained by reacting hexamethylene diisocyanate with a polyhydric alcohol, a dimer of hexamethylene diisocyanate, and a hexa A trimeric body of decyl diisocyanate or the like. The crosslinking agent (C) is usually used in an amount of from 0.1 to 5 parts by weight, based on 100 parts by weight of the acrylic resin (A) (the total weight when two or more types are used). The ratio is divided around. When the amount of the crosslinking agent (the amount of ruthenium is 〇. 〇) or more by weight based on 100 parts by weight of the acrylic resin (A), the durability of the pressure-sensitive adhesive layer tends to be improved, so that it is preferably 10 weights. When the amount of the optical film with an adhesive is less than that of the liquid crystal display device, the white dot-like eclipse becomes insignificant. Therefore, the resin film with an adhesive of the present invention has an adhesive layer. When the side is attached to the glass substrate, in order to improve the adhesion between the adhesive layer and the glass substrate on the adhesive for forming the adhesive layer, it is preferable to contain the compounding compound, especially in the blending It is more preferable to contain a decane-based compound in the acrylic resin before the crosslinking. Examples of the hetero compound are, for example, vinyl trimethoxy hydride, acetamethylene diethoxy sylvestre, and vinyl ginseng (2'). Methoxyethoxy) calcined, N-(2-aminoethyl)_3-aminopropylmethyldimethoxycarbazide, ^ (aminoethyl)·3·aminopropyltrimethyl Oxyl money, 3 · aminopropyl triethoxy = digan: oxypropyl trimethoxy dream burning, 3 - glycidol 孽 soil - methoxy oxime, 2-(3,4-epoxycyclohexyl)ethyltrimethyl hydride 320560 23 200920811 decyl, 3-chloropropyl decyl decyloxy decane, 3-chloropropyl three曱oxydecane, 3-methacryloxypropyltrimethoxydecane, 3-hydrothiopropyltrimethoxydecane, 3-glycidoxypropyltriethoxysulfonate, 3-shrinkage Glyceroxypropyl dimethyl fluorenyl sulfonyl sulphate, 3-glycidoxy propyl ethoxy dimethyl decane, etc. Two or more kinds of sinter calcined compounds can also be used. When it is represented by a (meth) oligomer, when the polyoxoxime oligomer is represented by a (monomer) oligopolymer, for example, the following may be mentioned. For example, 3-nitrothiopropyl group Trimethoxy methoxy-tetramethoxy pulverized copolymer, 3-hydrothiopropyltrimethoxy decane-tetraethoxy decane copolymer, 3-hydrothiopropyltriethoxy a hydrothiopropyl-containing copolymer such as a decane-tetradecyloxydecane copolymer, a 3-hydrothiopropyltriethoxydecane-tetraethoxydecane copolymer; Tris-methoxydecane-tetradecyloxydecane copolymer, thiol-decyltrimethoxydecane-tetraethoxydecane copolymer, thiol-decyltriethoxydecane-tetramethoxy a hydrothiomethyl-containing copolymer such as a decane copolymer, a thiol-decyltriethoxy decane-tetraethoxydecane copolymer; such as 3-mercaptopropoxypropyl propyl曱 矽 矽 - - tetradecyloxydecane copolymer, 3-mercapto propylene methoxy propyl trimethoxy decane - tetraethoxy decane copolymer, 3-methyl propylene methoxy propyl three Ethoxy decane-tetradecyloxydecane total 24 320560 200920811 polymer, '3-methylpropenyloxypropyltriethoxydecane-tetraethoxydecane co-polymer, 3-mercaptopropene oxime Oxypropyl decyl dimethoxy decane-tetramethoxy fluorinated copolymer, 3-mercapto propylene methoxy propyl decyl decyloxy decane-tetraethoxy fluorene copolymer, 3-Methyl propylene methoxy propyl methyl diethoxy decane - tetramethoxy fluorene terpolymer, 3-methyl propylene methoxy propyl methyl diethoxy decane - tetraethoxy矽a copolymer containing a methacryloxypropyl group such as a copolymer; such as a 3-propenyloxypropyltrimethoxydecane-tetradecyloxydecane copolymer, 3-propenyloxypropyl Trimethoxy decane-tetraethoxy oxime copolymer, 3-propenyl methoxypropyl triethoxy decane-tetradecyloxydecane copolymer, 3-propenyloxypropyl triethoxy Alkane-tetraethoxydecane copolymer, 3-propenyloxypropyl-decyldimethoxydecane-tetradecyloxydecane copolymer, 3-propenyloxypropylmethyldimethoxy Alkane-tetraethoxydecane copolymer, 3-propenyloxypropylmethyldiethoxydecane-tetradecyloxydecane Total 25 320560 200920811 Polymer, 3-propenyloxypropylmethyl a copolymer containing a propylene methoxy propyl group such as a diethoxy decane-tetraethoxy decane copolymer; such as a vinyl trimethoxy decane-tetradecyl decane copolymer, + ethyl meth Oxyfine crumb - tetraethoxy calcined copolymer, vinyl triethoxy decane-tetramethoxy decane copolymer, vinyl triethoxy decane - Ethoxy decane copolymer, vinyl mercapto dimethoxy decane-tetradecyl decane copolymer, vinyl mercapto dimethoxy decane-tetraethoxy decane copolymer, vinyl fluorenyl a copolymer containing a vinyl group such as a diethoxynonane-tetradecyloxydecane copolymer, a vinyl fluorenyl diethoxy decane-tetraethoxy oxane copolymer; for example, 3-aminopropyl Tris-decyloxydecane-tetradecyloxydecane copolymer, 3-aminopropyltrimethoxyoxane-tetraethoxydecane copolymer, 3-aminooxypropyltriethoxydecane- Tetramethoxydecane copolymer, 3-aminopropyltriethoxydecane-tetraethoxydecane copolymer, 3-aminopropylmercaptodimethoxydecane-tetradecyloxydecane Polymer, 3-aminopropylmethyldimethoxydecane-tetraethoxythorium terpolymer, 3-aminopropylmercaptodiethoxydecane-tetradecyloxydecane copolymer, An amine group-containing copolymer such as a 3-amino group, a propyl fluorenyl diethoxy group, a tetraethoxy decocted copolymer or the like; and these decane compounds are mostly liquid. The amount of the decane-based compound to be added to the adhesive is 100 parts by weight based on the non-volatile content of the acrylic resin (A) (the total weight when two or more types are used), and is usually 26 320560 200920811 0.01 to 10 It is preferably used in a ratio of about 0.05 to 5 parts by weight, based on the parts by weight. When the amount of the non-volatile enthalpy of the acrylic resin is 0.01 part by weight or more, the adhesion between the adhesive layer and the glass substrate is improved, which is preferable. Further, when the amount is 10 parts by weight or less, the decane-based compound tends to be prevented from flowing out of the adhesive layer, which is preferable. In the above-described adhesive, a cross-linking catalyst, a weathering stabilizer, a tackifier, a plasticizer, a softener, a dye, a pigment, an inorganic filler, a resin other than the acrylic resin (A), or the like may be further blended. Further, an ultraviolet curable compound is blended in the adhesive, and after the adhesive layer is formed, the ultraviolet ray is irradiated and cured to form a hard adhesive layer. Wherein, if the crosslinking agent and the crosslinking catalyst are simultaneously formulated in the adhesive, the adhesive layer can be prepared by the aging of the adhesive in a short period of time, and the resin attached to the adhesive can be inhibited in the resin film and adhered. The phenomenon of floating or peeling occurring between the agent layers, the foaming generated in the "agent layer", and the reworkability are also more favorable. As the cross-linking catalyst, for example, hexamethylene diamine B: amine, polyethylenimine, hexamethylenetetramine, di-ethyltriamine, dimethylamine: Preferably, the ketone diamine, the trimethylene diamine, and the polyamine-based tree cross-linking catalyst are compounded. ^ Liancai uses an isocyanate-based compound as an adhesive to form an adhesive composition, and forms an adhesive layer in a state where it is widely dissolved in a solvent. The substrate is coated on the substrate and dried to become 320560 27 200920811. The resin film of the adhesive of the present invention is produced in the production of β$ 〇. The viscous agent layer is in such a manner that the gel fraction is in the range of 50 to 99% by weight. The gel fraction is a value measured by the following (I) to (IV). And, the adhesive layer of about 8 (four) about 8 cm is bonded to the metal mesh (the weight of which is made diligent) by the SU of the center (10). = Weighing the above (1): the weight of the resulting composition, the weight of which is taken as I-man, folding the field in a manner to surround the adhesive layer - and the 4-person is stapled (Stapler) After living, weigh it and its weight is taken as Wb. =) Place the above (11) in a glass container to nail the mesh of the "i^:: force: into 60 W of ethyl acetate and impregnate it, and store it at room temperature for 3 days. ^ (IV) From The glass container was taken out of the glass container, dried for 12 hours, and weighed. The weight was taken as Wa, and the gel fraction was calculated according to the following formula: 'The amount of gel robes%MiWa_(Wb_Ws)_Wm}/(Ws_Wm )] When the gel fraction of the adhesive layer is 5 Gg or more, the durability tends to increase due to the adhesive layer, so it is better, and the gel fraction is less than or equal to the weight%. It is easy to manufacture, so it is better. The gel fraction of the adhesive layer is adjusted to 5 〇 to 99 wt.%, although it depends on the effective 9-point acrylic resin of the adhesive layer. However, if the amount of cross-linking agent is increased, the gel fraction will be changed to two. Therefore, it is preferable to adjust the gel fraction according to the amount of the cross-linking agent. Specifically, θ is the layer of the adhesive. The non-volatile content of the acrylic resin is 1 part by weight (the total amount is 2 or more), and the amount of the crosslinking agent is in the range of about 0.1 to 1 part by weight. With acrylic type 320560 28 200920811. Resin type t can be selected as appropriate. The gel fraction of the adhesive layer is on the "6 cc / 〇乂 (better than 75 reset 〇 / 较佳) and at 95 The resin film with an adhesive according to the present invention is provided with an adhesive layer formed of the above adhesive composition on at least one surface of the resin film. The resin film to be used herein may, for example, be a film containing a film selected from a polarizing film or a retardation film, or be bonded to an optical film as a protected object. A surface protective film or the like which is used for the purpose of protecting the surface from damage, contamination, etc. The polarizing film is an optical film having a function of emitting polarized light with respect to incident light such as natural light. Type: a linear material that absorbs a vibrating surface in a certain direction, and has a linear polarizing film that penetrates a linear polarized light having a vibrating surface perpendicular thereto; and reflects linear polarized light having a vibrating surface in a certain direction, and has Have a vertical a polarizing separation film having a property of linearly polarizing light of a vibration surface; a circularly polarizing film formed by a polarizing film and a retardation film to be described later, etc. A polarizing film, in particular, a straight line. A polarizing film (which may be called a polarizing film, A suitable example of the polarizing film is a dichroic dye such as an iodine or a dichroic dye which is adsorbed and aligned in a polyethylene resin film which is stretched in one axis. Refers to an optical film exhibiting optical anisotropy, which may be, for example, polyvinyl alcohol, polycarbonate, polyester, polyacrylic acid, polyimine, polystyrene, cyclic polyolefin, polystyrene, PolysulW, poly_hard I partial ethylene/polymethyl methacrylate, liquid crystal polyacetate, acetic acid 320560 29 200920811 cellulose, ethylene-vinyl acetate copolymer saponification, polyglycolized ethylene The polymer film formed by the method is extended by about 101 to 6 times to obtain a stretch film. Among them, a polymer film obtained by stretching a single axis or biaxially stretching a polycarbonate film or a cyclic polyolefin film is preferred. The one-axis retardation film is also called a wide viewing angle retardation film, a low photoelasticity retardation film, etc., but can be suitably used for any of them. In addition, optical anisotropy is exhibited by coating and alignment of a liquid crystal compound! The film of the raw film or the film exhibiting optical anisotropy by coating with an inorganic layered compound can be used as a retardation film. In the case of such a retardation film, there is also a film called a temperature-compensated retardation film, and a film obtained by twist-aligning a rod-shaped liquid crystal, which is sold under the trade name "LC film" by Nippon Oil Co., Ltd. The brand of Nippon Oil Co., Ltd. sells the product of the "Simplified Film", which is sold under the slanting alignment of the rod-shaped liquid crystal, and the XWV film of Fujifilm Co., Ltd. (4) :=, Sumitomo Chemical Co., Ltd., a shaft-aligned film sold under the trade name "VAC film", and a biaxial alignment type film sold by Sumitomo Chemical Co., Ltd. under the trade name "New VAC Film". 」 作 Ϊ Ϊ Ϊ : : : : : : : : 在 在 在 在 在 在 在 在 在 在 在 在 在 在 在 在 在 在 在 在 在 在 在 光学 光学 光学 光学 光学 光学 光学 光学 光学 光学 光学 光学Polymethyl phthalate, glycerin, polyester resin, polyolefin tree, _resin, poly gambling, etc. in the protective film Yang Yi § 糸 糸 compound, benzophenone compound, benzene And three saliva prices 320560 30 200920811 • mouth / dimer compounds, cyanoacrylate compounds, zinc into the private salt compounds "outside, (four) (four). The protective film is preferably an acetaminophen-based resin film such as a plain film. In the above optical film, the linear polarizing film is a single-sided polarizing film (for example, a polyvinyl alcohol-based resin is formed into a κ8 or a double-sidedly coated Mogubit # / Wuxian film) Or the surface is covered with a protective film to use. In addition, the polarizing film is composed of a linear polarizing film and a retardation film = two: a protective film is attached to one or both sides of the polarizing film: "On the ellipsic film" In the present invention, an adhesive layer is formed, and an adhesive layer is usually formed on the retardation film side. The surface protective film is a film used for the purpose of protecting an optical film or the like as a protected body from surface damage or contamination. For example, various optical films such as a polarizing film, a retardation film, a light diffusion sheet, and a reflective sheet used in the production of a liquid crystal display I are used on the surface thereof (when the adhesive layer is provided on one side, it means The adhesive layer is on the opposite side, and the surface protective film is bonded to the surface, and after being bonded to the liquid crystal cell or the like, the surface protective film is usually removed. The substrate of the surface protective film may be, for example, Listed: such as polyethylene, polypropylene: / # 'poly-p-butyl baking such as poly-smoke resin; such as poly-gasification, χ 偏 偏 一 氟 i i i 、 聚 聚 、 、 、 、 、 、 、 、 、 、 、 、 、 、 Fluorinated polyolefin resin; such as polynaphthalene Acid ethylene carbonate (p〇lyethylene Naphthalate), polyethylene terephthalate stupid two Yue acid (p〇lyethylene

Terephthalate)、聚對苯二甲酸丁二酯、聚對苯二甲酸乙二 酯/間苯二曱酸酯共聚合物等聚酯系樹脂;如尼龍6、尼龍 6,6等聚醯胺,如聚氯化乙烯、.氣化乙烯-乙酸乙烯酯共聚 31 320560 200920811 合物、乙婦-乙酸乙烯酯共聚合物、乙稀-乙婦醇共聚人物、 :聚乙_、維尼綸(vinylon)等乙烯聚合物;三乙酸纖 •=酸纖維素、赛路紛㈣一_)等纖維素系、樹脂;如聚 甲基丙烯酸甲I旨、聚甲基丙稀酸乙醋、聚丙婦 =烯,丁酯等丙烯㈣樹脂;其他,如聚苯乙烯、聚碳酸 ^、聚芳酯(p〇1yarylate)、聚醯亞胺等。 貼明之附黏著劑之樹崎,在其黏著劑層表面是 =剝離膜’直到使用為止以暫時接著保護為宜。在賴 聚對苯二甲酸丁二醋、聚碳酸二酿、聚、 t作為基材,在與此基材的黏㈣I層接合之面上,妳 進盯如.聚矽氧處理等離型處理者等。 、 上劑之樹腊膜可藉由例如下述方法而製造:在如 上述之剝離膜上’塗布前述 μ \ ^ ^者绡、、且成物而形成黏著劑 層並在所得之黏著劑層上再積 $ ::二布黏著劑組成物而形^ 保護,作成附黏著劑之樹脂膜“ 為宜=巧之厚度並無特別限定’通常是在30心以下· 黏著1G/Zm以上較佳,更佳是在1()至·m。 提高,破璃其;间卩皿鬲濕下之接著性會 有降低ί傾ί層之間發生浮起或剝落之可能性 厚:亚且重加工性有提高之傾向,故較佳,另 /子度在10 # m以上時,卽 尺寸有變化,黏著劑層、σ於其上之光學膜的 a Θ k心著此尺寸變化而變動,故 320560 32 200920811 'St?部的明亮度與中心部之明亮度之間變成沒 .自以 ’’’、占’缺色或顏色不均有被抑制之傾向,故較佳。 ^ ^ ^在液晶單元玻璃上所貼著之黏著劑層的 乂子度雖以25 // m a押、、隹 /丄, 、 為払準,但在本發明中,即使此厚度在20 m以下’也旎充分發揮作為黏著劑層之性能。 作之附黏著劑之樹脂膜,係在貼著於玻璃基板而 =!積層體後,在有任何之不合適狀況而將該樹脂膜 =璃基板剝離時,黏著劑層是會隨著樹脂膜而被剝離, 著劑層相接之玻璃基板的表面,因幾乎不會發生截 沾糊殘留等現象’故剝離後之玻璃基板可很容易地重 新貼著附黏著劑之樹脂膜。亦即,重加工性優異。 [光學積層體] 本發明之附黏著劑之樹脂膜,係可由光學膜來構成樹 曰、,亚以其黏著劑層積層在玻璃基板上,而製成光學積 二:1若要在玻璃基板上將附黏著劑之光學膜予以積層而 =成光學積層體’則例如可從如上述所得之輯著劑之樹 2關去_膜’並將露出之黏著劑層貼合在玻璃基板之 Λ面即可。在此,作為玻璃基板者可列舉如:液晶單元之 ,,基板、防眩用玻璃、太陽眼鏡用玻璃等。其中,在液 =單7G之别面側(視認側)之玻璃基板上積層附黏著劑之光 于膜(上偏光膜)後,在液晶單元之背面側之玻璃基板上積 =別的附黏著劑之光學膜(下偏光膜)而製成的光學積層 版係因可作為液晶顯示裝置來使用,故較佳。玻璃基板 之材料例如可列舉:鈉鈣玻璃(soda-lime glass)、低鹼玻 320560 33 200920811 璃、無驗破場等。 本發明之光學積層體是可作為液 元使用。 晶顯示裝置之液 θ 日日旱 1月之先予積層體所形成之液晶 可用在包括筆記型、卓而刑ρηΛ“ 例如 人m曰 桌面型、PDA(個人數位助理)等的個 电月自用液曰曰顯示器、、電視、車輛用顯示器、電血 數位相機、數位錄影機、f子桌上計算機、鐘錶等/、Terephthalate), polybutylene terephthalate, polyethylene terephthalate / isophthalic acid ester copolymer, and other polyester resins; such as nylon 6, nylon 6,6 and other polyamines, such as Polyvinyl chloride, gasification ethylene-vinyl acetate copolymer 31 320560 200920811 compound, ethylene-vinyl acetate copolymer, ethylene-ethyl alcohol copolymerization characters, polyethylene _, vinylon (vinylon), etc. Ethylene polymer; triacetate fiber == acid cellulose, raceway (4) a) cellulose and other resins; such as polymethyl methacrylate, polymethyl methacrylate, polypropylene propylene = ene, Propylene (tetra) resin such as butyl ester; other, such as polystyrene, polycarbonate, polyarylate (p〇1yarylate), polyimine, and the like. The paste with the adhesive attached is = peeling film on the surface of the adhesive layer until it is used for temporary protection. In the case of lysine polybutylene terephthalate, polycarbonate, poly, t as a substrate, on the surface of the bonded (four) I layer of the substrate, the intrusion is treated as a polyether treatment. And so on. The wax film of the upper agent can be produced, for example, by coating the above-mentioned film on the release film as described above, and forming an adhesive layer on the obtained adhesive layer. Re-stacking the composition of the $:2 cloth adhesive and protecting it as a resin film with an adhesive. "The thickness of the film is not particularly limited." It is usually below 30 centimeters. It is better to adhere to 1G/Zm or more. More preferably, it is in the range of 1 () to · m. It is improved, and the adhesion between the layers of the dish is reduced. The possibility of floating or peeling between the layers is thick: sub-heavy processing The tendency to improve is preferred, and when the other side is above 10 #m, the size of the crucible changes, and the adhesive layer and the a Θ k of the optical film on which the σ is applied vary with the change in size. 320560 32 200920811 'The brightness between the St? part and the brightness of the center part becomes no. The self-conceived ''', the lack of color or the color is not suppressed, so it is better. ^ ^ ^ in the LCD Although the degree of the enthalpy of the adhesive layer adhered to the unit glass is 25 // ma, 隹/丄, 払, in the present invention, When the thickness is 20 m or less, the performance of the adhesive layer is also sufficiently exhibited. The resin film to which the adhesive is attached is attached to the glass substrate and is not suitable for the laminate. When the resin film is peeled off from the glass substrate, the adhesive layer is peeled off along with the resin film, and the surface of the glass substrate where the agent layer is in contact with each other is hardly caused by the phenomenon that the paste remains or the like. The glass substrate can be easily reattached to the resin film with the adhesive. That is, the reworkability is excellent. [Optical laminate] The resin film of the adhesive of the present invention can be composed of an optical film to form a tree, An optical product is formed by laminating an adhesive on a glass substrate: 1 to laminate an optical film with an adhesive on a glass substrate to form an optical laminate, for example, from the above The agent tree 2 is closed to the film _ and the exposed adhesive layer is bonded to the surface of the glass substrate. Here, as the glass substrate, for example, a liquid crystal cell, a substrate, and an anti-glare glass , glass for sunglasses, etc. On the glass substrate on the other side of the liquid (single side) (on the side of the viewing side), the light of the adhesive is laminated on the film (upper polarizing film), and then on the glass substrate on the back side of the liquid crystal cell, another adhesive is attached. The optical laminated plate made of the optical film (lower polarizing film) is preferably used as a liquid crystal display device, and examples of the material of the glass substrate include soda-lime glass and low alkali glass 320560. 33 200920811 Glass, no test break, etc. The optical laminate of the present invention can be used as a liquid element. The liquid crystal of the crystal display device θ The liquid crystal formed by the laminate in January and the first month can be used in the notebook type including And the sentence ρηΛ "for example, a person's desktop computer type, PDA (personal digital assistant), etc., a monthly liquid-use liquid display, television, vehicle display, electric blood digital camera, digital video recorder, f sub-desk computer, Clocks, etc.

诉2 ’縣實施例更具體說明本發明,但本發明並不 4之例子。例中,使用量及含有量是用「份」及「% 表不,無特別論述時為重量基準。 0J 在以下例子令,不揮發分係根據JISK54〇7之方法 ,定之值。具體而言’以任意之重量裝取黏著劑溶液到培 養皿中’在防爆爐中於115t乾燥2小時後秤量殘留之不 揮發分之重量,將其相對於最初測定之溶液重量以比率來 表不者。另外’重量平均子量之測定是在Gpc裝置中.,以 串聯2枝東曹公司製的“TSK gd Gmhhr_h(s)”作為管柱 而配置,在使用四氫吱喃作為溶出液、試料濃度5 mg/⑹、 試料導入量100# 1、溫度401、流速l ml/分鐘之條件下 進行標準聚苯乙烯換算。 : , 首先,表示丙烯酸系樹脂之製造例。 [聚合例1] 在附有冷凝管、氮氣導入管、溫度計及攪拌機之反應 容器中,放入乙酸乙酯81.8份、丙烯酸丁酯98.6份、丙 埽酸2-羥基乙酯1.0份及丙烯酸〇·4份之混合溶液,以氮 320560 34 200920811 - 氣取代裝置内之空氣而使其不含有童遙 m 士 ’乳軋,同時使内溫上昇 '到55°C。之後,添加由偶氮雙異丁睛(聚合起始劑从…分 溶解到乙酸以旨H)份中而成之溶液之全量。起始劑添力^ 小時後,以使除去單體之丙烯酸系樹脂的濃度變成之 Μ ’在添加4度Π.3份/小時下’—面連續將乙酸乙酉旨 加入反應谷态中,一面使内溫保溫在5 4至5 6。〇之間12小 時,最後,加入乙酸乙酯,使丙烯酸系樹脂之濃度調整成 ,20%。所得之丙烯酸系樹脂藉纟Gpc換算成聚苯乙稀的重 (量平均分子量Mw為1,230,000,Mw/Mn為3 9。將此當作 丙烯酸系樹脂A1。丙烯酸系樹脂入丨中,源自屬於含有羥 基之單體的丙婦酸2·羥基乙酯之結構單元為1%,同時,— 源自屬於含有羧基之單體的丙烯酸之結構單元為〇.4%。 [聚合例2] 除了將單體鈕成變更成乙酸.乙酯8〇份、丙烯酸丁酯 78.6份、丙烯酸曱醋2〇 〇份、丙烯酸2_羥基乙酯份, I及丙烯酸〇,4份之外,其餘與聚合例丨同樣操作,製造丙 烯酸系樹脂。所得之丙烯酸系樹脂藉甴Gpc換.算成聚苯乙_ 烯的重量平均分子量Mw為1,648,000,Mw/Mn為4.1。將 此當作丙稀酸系樹脂A2。丙烯酸系樹脂A2中,也是源| 屬,s有赵基之單體的丙稀酸2_經基乙酯之結構單元之比 ¥為1 /〇,源自屬於含轰基之單體的丙稀酸之結構單元之 比率為0.4¾ 〇 _ 一 其次’使用上述製造之丙烯酸系樹脂調製黏著劑,例 y 一、t用於光學膜之實施例及比較例。在以下之例中,作為 35 320560 200920811 離子性化合物者是便用以下之物質。各化合物之記號係為 _ 了在後參考而附上者,稱為離子性固體i至離子性固體5 之化合物係在25°C室溫中為固體者’稱為離子性液體^ 化合物係在25°C之室溫中為液體者。 離子性固體1 :六氟磷酸N_ 丁基_4_甲基吡啶鏽鹽(具 有下式之結構,熔點481:) ch3~^^N - (CH2)3CH3 PF6*~ 離子性固體2:六氟磷酸N-己基吡啶鑌鹽(具有下式之 結構,熔點45。〇The invention is more specifically described in the 2's embodiment, but the invention is not in the example of 4. In the example, the amount of use and the amount of the content are expressed in terms of "parts" and "%". Unless otherwise stated, the weight is used. 0J In the following example, the non-volatile fraction is determined according to the method of JISK54〇7. Specifically, 'Adsorb the adhesive solution to the culture dish at an arbitrary weight'. After drying at 115 t for 2 hours in an explosion-proof furnace, the residual non-volatile weight was weighed and expressed as a ratio with respect to the initially measured solution weight. In addition, the measurement of the weight average amount is carried out in a Gpc apparatus, and is carried out by using "TSK gd Gmhhr_h(s)" manufactured by Tosoh Corporation in tandem as a column, and tetrahydrofuran is used as an eluate and a sample concentration. 5 mg/(6), the sample introduction amount 100#1, the temperature 401, and the flow rate of 1 ml/min were measured in standard polystyrene. First, the production example of the acrylic resin was shown. [Polymerization example 1] In a reaction vessel of a condenser, a nitrogen inlet tube, a thermometer, and a stirrer, a mixed solution of 81.8 parts of ethyl acetate, 98.6 parts of butyl acrylate, 1.0 part of 2-hydroxyethyl acrylate, and 4 parts of ruthenium acrylate was placed. Nitrogen 320560 34 200920811 - The air replaces the air in the device so that it does not contain the child's milk, while the internal temperature rises to 55 ° C. After that, it is added by azobisisobutyl phthalate (polymerization initiator from ... The total amount of the solution obtained by the acetic acid in the H) part. After the initiator is added for a period of time, the concentration of the acrylic resin to remove the monomer is changed to Μ 'after adding 4 degrees Π.3 parts/hour. The surface was continuously added to the reaction state, and the internal temperature was kept at 5 4 to 5 6 for 12 hours. Finally, ethyl acetate was added to adjust the concentration of the acrylic resin to 20%. The obtained acrylic resin was converted into polystyrene by Gpc (the average molecular weight Mw was 1,230,000, and Mw/Mn was 39. This was regarded as the acrylic resin A1. The acrylic resin was introduced into the crucible, derived from The structural unit of 2-hydroxyethyl acetoacetate which is a monomer having a hydroxyl group is 1%, and at the same time, the structural unit derived from acrylic acid which is a monomer having a carboxyl group is 4. 4%. [Polymerization Example 2] The monomer button was changed to acetic acid. Ethyl ester 8 parts, butyl acrylate 78.6 parts, acrylic vinegar 2 An acrylic resin was prepared by the same operation as in the polymerization example except that the hydrazine, the 2-hydroxyethyl acrylate portion, the I and the hydrazine acrylate were used in the same manner as in the polymerization example. The obtained acrylic resin was converted into a polystyrene by the Gpc. The weight average molecular weight Mw of the olefin is 1,648,000, and Mw/Mn is 4.1. This is regarded as the acrylic resin A2. In the acrylic resin A2, it is also a source | genus, and s has a monomeric acrylic acid of Zhaoji 2 The ratio of the structural unit of _ benzyl group is 1 / 〇, and the ratio of the structural unit derived from the acrylic acid which is a monomer containing a fluorenyl group is 0.43⁄4 〇 _ _ _ followed by 'modulation using the acrylic resin produced above Adhesives, Examples y I, t Examples of optical films and comparative examples. In the following examples, the following substances are used as the ionic compound of 35 320560 200920811. The symbol of each compound is _ which is attached later, and the compound called ionic solid i to ionic solid 5 is solid at room temperature at 25 ° C, which is called an ionic liquid. It is liquid at room temperature of 25 °C. Ionic solid 1: hexafluorophosphate N-butyl_4-methylpyridyl rust salt (having the structure of the following formula, melting point 481:) ch3~^^N - (CH2)3CH3 PF6*~ ionic solid 2: hexafluoro N-hexylpyridinium phosphate salt (having the structure of the following formula, melting point 45.

-(CH2)5CH3 PF, 離子性固體3 :六氟磷酸N-辛基-4-甲基吡啶鎮鹽(具 有下式之結構,熔點44。〇 . . . . · CH3-^N-(CH2)7CH3 pf6~ , · (具有 離子性固體4:六氟磷酸1-曱基-3-乙基咪唑鐵 下式之結構,熔點62。〇 pf6' CHrN^N - CH2CH3 離子性固體5 :六氟磷酸四丁基銨鹽(具有下式之結 構’熔點78°C ) 320560 36 200920811 (CH2)3CH3 PFs CH3(CH2)3 N一(CH2)3CH3 (CH2)3CH3 離子性液體1 :六氟磷酸N-己基-4-曱基吡啶鑌鹽(具 有下式之結構,熔點18°C) CH3-H0Kj-(CH2)5CH3 PF6 - 另外,交聯劑及石夕烧系化合物係使用以下者(任何一種 皆為商品名)。 〈交聯劑〉-(CH2)5CH3 PF, ionic solid 3: N-octyl-4-methylpyridine hexafluorophosphate (having the structure of the following formula, melting point 44. 〇. . . . . CH3-^N-(CH2 ) 7CH3 pf6~ , · (having an ionic solid 4: hexafluorophosphate 1-mercapto-3-ethylimidazolium iron having the following formula, melting point 62. 〇pf6' CHrN^N - CH2CH3 ionic solid 5: hexafluoro Tetrabutylammonium phosphate (structure with the following formula 'melting point 78 ° C) 320560 36 200920811 (CH2)3CH3 PFs CH3(CH2)3 N-(CH2)3CH3 (CH2)3CH3 Ionic liquid 1: Hexafluorophosphate N -hexyl-4-mercaptopyridinium salt (having the structure of the following formula, melting point 18 ° C) CH3-H0Kj-(CH2)5CH3 PF6 - In addition, the crosslinking agent and the ceramsite compound are the following (any one All are trade names).

Takenate D160N :六亞甲基二異氰酸酯之三羥曱基丙烷 加成物的乙酸乙酯溶液(固形分濃度75%),取自三井 化學 Polyurethane 公司。Takenate D160N: Ethyl acetate solution of hexamethylene diisocyanate trishydroxylpropane adduct (solids concentration 75%) taken from Mitsui Chemicals Polyurethane.

Coronate L :伸曱苯二異氰酸酯之三羥曱基丙烧加成物 的乙:酸乙酯溶液(固形分濃度75%),取自日本Poly urthane 公司。 〈矽烷系化合物〉 KBE-402 :縮水甘油氧基丙基二乙氧基曱基矽烷(液 體),取自信越化學工業公司。 KBE-403 :縮水甘油氧基丙基三曱氧基矽烷(液體),取 自信越化學工業公司。 [實施例1至5及比較例1至3] (a)黏著劑之製造 37 320560 200920811 相對於聚合例i所得之丙烯酸系樹脂A1之 :份分交聯劑「TakenateD160N」之固形分、〇刀0 • ::=ίΐ:ΚΒΕ’2、及表1所示之離子性化合物各: 所不&lt; 里轧合,再以使固形分濃度變成13%之 酸乙醋’作成黏著劑組成物。 口乙 表1 例No. 實施例1 實施例2 實施例3 實施例4 實施例5 比較例 比較例2 比較例3Coronate L: Ethyl acetate solution (solids concentration: 75%) of trishydroxyl-propyl hydride adduct of phenyl diisocyanate, taken from Polyurman Company, Japan. <decane-based compound> KBE-402: glycidoxypropyldiethoxydecyldecane (liquid), taken from the chemical industry company. KBE-403: glycidoxypropyl trimethoxy decane (liquid), take the confidence of the chemical industry company. [Examples 1 to 5 and Comparative Examples 1 to 3] (a) Production of Adhesive 37 320560 200920811 Relative to Acrylic Resin A1 obtained in Polymerization Example i: Solid component of split crosslinking agent "Takenate D160N", file 0 • ::= ΐ: ΚΒΕ '2, and each of the ionic compounds shown in Table 1: The mixture was not rolled in, and the composition was made of an acid vinegar having a solid content of 13%. Mouth Table 1 Example No. Example 1 Example 2 Example 3 Example 4 Example 5 Comparative Example Comparative Example 2 Comparative Example 3

性化合叙(種類/臺I 性固體—1/1.0份 離子性固體2/1.0份 離子性固體3/1.0份 離子性固體4/1,0份 離子性固體5/1.0份 液體 1/1.0 份 離子性固體3/0.1份 離子性固體3/10.0份Sexualization (type/set of I-solids - 1 / 1.0 part ionic solid 2 / 1.0 part ionic solid 3 / 1.0 part ionic solid 4 / 1, 0 part ionic solid 5 / 1.0 part liquid 1 / 1.0 part Ionic solid 3/0.1 part ionic solid 3/10.0 parts

(b)附黏著劑之樹脂膜之製作 將上述各黏著劑組成物,在經離型處理之聚對笨二甲 酸乙二酯膜(商品名“PET 3 81.1”,取自Lintec公司;稱為隔 離膜(separator))之離型處理面上,使用塗布機並以使乾燥田 後^厚度成為m之方式塗布,在9〇t:乾燥i分鐘,得 到薄片狀之黏著劑。其次,將吸附配向有碘之聚乙烯醇偏 光片之兩面以由三乙醯纖維素所成之保護膜挾住,而製成 3層結構的偏光膜,在該偏光膜之單面上,將上述所得之 薄片狀黏著劑的與隔離膜為相反側之面(黏著劑面)藉由積 320560 38 200920811 ' · :機而貼σ之後’於溫度23。〇、相對濕度之條件下使 :天、’即可得附黏著劑之偏光膜。對於硬化後之各 .-者背θ u上述方法測定凝膠I率,其結果顯示在表2 τ 。 (c)附黏著劑之樹脂膜之抗靜電性評估 田剝離所付之附黏著劑之偏光膜的隔離膜時,將黏著 面電阻值以表面固有電阻測定裝置[三菱化學公司 :=品名為“Hirest,⑽姻5〇 ”]測定,評估抗靜電 ^表面電阻值若為10ηΩ/口等級或其以下之值,即可得 二電性:抗靜電性之評估,係在附黏著劑之偏光 存 :成之後’立即進行。另外,為了要觀察長期保 存日τγ的經時變化.,將ρ 士 士 4 將已凡成硬化之附黏著劑之偏光膜在溫 二、相對濕度70%之爐中保管6天後,與上述相同地 。㈣隔離膜,'測定黏著劍之表面電阻值。在此,於溫度.的 6個月目對^ 7〇%下保管6天,係可得與「在室溫下保管 個月」成乎相同之效果。將結果整理在表2中。 (d)光學積層體之製作及評估 嗲腺自^梯)所製作的附黏著劑之偏光膜剝離隔離膜 之™,(商;用玻璃基 與穑;甘 、 2作光學積層體。有關此光 _驗時:二。保管3。〇嫩 3〇〇 J日士、次在/皿度6〇C、相對濕度90%之條件下保管 3〇U小日可進行耐濕熱試驗時, θ 了次將仉加熱成7CTC之狀態降 / J c再汁㈣赃之過程當作.1個循環(1小時)並反 320560 39 200920811 /主行100们循環而實施耐熱衝擊(heat shock)試驗時之各 .月;兄以目挪觀察各試驗後之光學積層體。將結果用以 -下之基準分類,整理在表2中。 熱及熱衝擊(在表2標記成「HS」)之耐久性的 β估基準&gt; I:完全看不到浮起、剝落、發泡等外觀變化。 j乎看不到浮起 '剝落、發泡等外觀變化。 :起、剝洛、發泡等外觀變化為有些明顯。 .浮起、剝落、發泡耸#麵Μ Λ ^ i [實施例6] …外硯變化為非常顯著。 严2於聚合例2所得之丙烯酸系樹脂A2之固形分1〇〇 知,將〇·5份交聯劑rc〇r〇 /刀100 烷系化合物“KBE-402”、及7 5 )之固形刀、〇.5份之矽 再以使固形分濃度變成.13%之二=生固體3予以混合, 黏著劑組成物。使用此科宴制/外加乙酸乙酯,而作成 相同之評估,將結果整理進行與實施例1至5 320560 40 200920811 表2 例No. 離子性 化合4之 狀態* 實施例1 實施例2 實施例3 實施例4 實施例5 實施例6 體體體體體體 固固固固固固 黏著劑 層之凝 膠分率 79.5 % 83.2 % 82.4 % 80.3 % 85.3 % 85.1 % 釗雜問隔膜時之夹面雷阳僧 初期 60t: X 6曰f糸 9.01X1010Q/D 1.1〇Χ1〇πΩ/Π 2.21Χ10πΩ/ϋ Ι^ΟΧΙΟ1^/^ 3. 87X10nQ/D 3. δΒΧΙΟ^Ω/Π Ι.βΟΧΙΟ1^/^ 2.41Xl〇1:LQ/n 6. 29X10nQ/D 5.12X101;lQ/n β.ΟΙΧΙΟ1^/^ β.δδΧΙΟ^β/Π 性久耐 ◎◎◎◎◎◎熱◎◎◎◎◎◎ 熱 濕 SΗ 〇〇〇◎〇0(b) Preparation of a resin film with an adhesive The above-mentioned adhesive composition is subjected to a release treatment of a polyethylene terephthalate film (trade name "PET 3 81.1", taken from Lintec; The release surface of the separator was applied by using a coater so as to have a thickness of m after drying, and dried at 9 Torr for 1 minute to obtain a sheet-like adhesive. Next, the two sides of the polyvinyl alcohol polarizer which is adsorbed and bound to the iodine are rubbed by a protective film made of triacetyl cellulose to form a polarizing film having a three-layer structure, and on one side of the polarizing film, The surface of the flaky adhesive obtained above is opposite to the separator (adhesive surface) by the product 320560 38 200920811 ': : after the σ is attached to the temperature 23 . Under the conditions of 〇 and relative humidity, it is possible to obtain a polarizing film with an adhesive. For each of the hardened samples, the gel I rate was measured by the above method, and the results are shown in Table 2 τ. (c) Antistatic property evaluation of the resin film with an adhesive When the separator of the polarizing film with an adhesive attached to the field is peeled off, the surface resistance is measured by a surface specific resistance measuring device [Mitsubishi Chemical Co., Ltd.: = product name" Hirest, (10) marriage 5 〇"] determination, evaluation of antistatic ^ surface resistance value of 10 η Ω / mouth level or below, you can get two-electricity: evaluation of anti-static properties, in the adhesion of the adhesive : After the completion 'immediately. In addition, in order to observe the change over time of the long-term storage day τγ, the polarizing film of the adhesive which has been hardened by 士士士4 is stored in a furnace of temperature two and a relative humidity of 70% for 6 days, and identically. (4) Isolation film, 'determine the surface resistance value of the adhesive sword. Here, it can be stored for 6 days at a temperature of 6 months, and it can be obtained in the same manner as "keeping at room temperature for 6 months". The results are organized in Table 2. (d) Fabrication and evaluation of optical laminates TM for polarizing film-separating separators with adhesives prepared by the sacral gland; (commercial; glass-based and enamel; gan, 2 as optical laminates. Light_Inspection time: 2. Storage 3. When the 〇 〇〇 〇〇 〇〇 〇〇 〇〇 、 、 、 、 、 、 、 、 、 、 、 、 、 、 、 、 、 、 、 、 、 、 、 、 、 、 、 保管 保管 保管 保管 保管 保管 保管 保管 保管 保管 可 可The process of heating the temperature to 7CTC is reduced / J c re-sap (4) 赃 is treated as 1 cycle (1 hour) and reverse 320560 39 200920811 / main row 100 cycles are subjected to heat shock test Each month, the brothers observed the optical laminates after each test. The results were classified by the following criteria and are listed in Table 2. Thermal and thermal shock (marked as "HS" in Table 2) β estimator> I: No change in appearance such as lifting, peeling, foaming, etc.. No visible change in appearance such as peeling, foaming, etc. It is somewhat obvious. Float, flaking, foaming #面Μ Λ ^ i [Example 6] ... The external enthalpy change is very significant. Strict 2 is obtained in Polymerization Example 2. The solid content of the acrylic resin A2 is known as a solid knife and a crucible of 5 parts of a cross-linking agent rc〇r〇/knife 100 alkane compound "KBE-402" and 7 5). Further, the solid content is changed to a concentration of .13% = raw solid 3, and the adhesive composition is mixed. Using this banquet system/external ethyl acetate, the same evaluation was performed, and the results were organized in the same manner as in Examples 1 to 5 320560 40 200920811 Table 2 Example No. Ionication 4 * Example 1 Example 2 Example 3 Example 4 Example 5 Example 6 Body body body solidification solidification adhesive layer gel fraction 79.5 % 83.2 % 82.4 % 80.3 % 85.3 % 85.1 % Nozzle surface when noisy The initial 60t of Leiyang 僧: X 6曰f糸9.01X1010Q/D 1.1〇Χ1〇πΩ/Π 2.21Χ10πΩ/ϋ Ι^ΟΧΙΟ1^/^ 3. 87X10nQ/D 3. δΒΧΙΟ^Ω/Π Ι.βΟΧΙΟ1^/^ 2.41Xl〇1: LQ/n 6. 29X10nQ/D 5.12X101; lQ/n β.ΟΙΧΙΟ1^/^ β.δδΧΙΟ^β/Π Sexual resistance ◎ ◎ ◎ ◎ ◎ ◎ ◎ ◎ ◎ ◎ ◎ ◎ ◎ ◎ SΗ 〇〇〇◎〇0

吏用之離子性化合物在25-C時之狀態 由表1及表2可知,相對於丙烯酸系樹脂1〇〇份, 配本發明所規定之離子性固體1份而構成黏著劑的實施 1至5、以及調配離子性固體7 5份而構成黏著劑的實施 6,與調配離子性液體之比較例!相比’不但在製作初期 表現同等之抗靜電性,同時即使放置長時間,1抗雷 也幾乎沒有變化,又’在雜性、耐㈣性及耐敎衝擊 方面也可得到令人滿足之結果。 + 甲其相對於此’调配25 c時為液體之六氟鱗酸N'己其乂 在衣作初期中顯不良好之抗靜電性,但於作. . 60t ^ 70〇/〇T^f 6 離隔離膜後之表面電阻值與初期之值相比變成“下,: 上方:確認到,長期保管而使抗靜電性有衰 一方面’由調配同樣之離子性固體3而改變其量之= 32〇56〇 41 200920811 3、比較例2及比較例3之結果,可知告 木^ J知虽相對於100份之石 烯酉义糸樹脂,離子性固體之調配量為〇 八士 丙 予抗靜電性之效果並不充足,另外,I 了則s使靖 一 田具I變成10份時, 顯示耐久性變得不充足之結果。 τ [產業上之可能利用性] 本發明之附黏著劑之樹脂膜,係可有效地抑制光 材之帶電。再者,自製作後即使長時間保管 期之抗靜電性能。 呆持初 此附黏著#1之樹賴,例如,係由光學臈來構成樹脂 膜,並藉由積層在液晶單元之玻璃基板上,而得到液晶顯 不用之光學積層體。此光學積層體在濕熱條件下,因為是 由黏著劑層來吸收/緩衝因光學膜及玻璃基板之尺寸變化疋 而引起之應力,故可減輕局部性的應力集中,並能抑制對 玻璃基板之黏.著劑層的浮起或剝離等。同時,因可防止由 不均勻之應力分布所引起的光學缺陷,故制白 色。再者,附黏著劑之樹脂膜一旦積層在玻璃 有任何不適當之情料,即使從玻縣板同時義此樹脂 膜及黏著劑’在剝,離後之玻璃基板表面亦很少會發生黏糊 殘留或穢垢之現象,並可再度作為玻璃基板使用,為重加 工性優異者。 另外,此附黏著劑之樹脂膜,.亦可作為貼合在光學膜 之表面而直到使用為止都保護著此表面之表面保護膜。在 此if形下,也可賦予優異之抗靜電效果,例如,將光學膜 隔著與表面保護膜為相反侧之黏著劑層而貼合在液晶單元 320560 42 200920811 後,將此表面保護膜剝離時,可使產生之靜電變 : 本發明之附黏著劑之樹脂膜,在賦予高抗靜=性之同 .時’還可長時間保持此抗靜電性,並且亦具有優異之耐久 性。此附黏著劑之樹脂膜係由光學膜來構成樹脂膜,而能 適用在液晶顯示裝置。另外,附黏著劑之樹脂膜也能適合 作為保護光學膜表面之表面保護膜使用。 【圖式簡單說明】 Μ 【主要元件符號說明】 320560 43The state of the ionic compound used in the case of 25-C is shown in Tables 1 and 2, and 1 to 5 of the acrylic resin is provided with 1 part of the ionic solid specified in the present invention to form an adhesive. And the preparation of the ionic solids with 75 parts of the ionic solids, and the comparison of the preparation of the ionic liquids! Compared with 'not only the same antistatic properties in the initial stage of production, but also for a long time, 1 anti-thunder has almost no change, and 'satisfying results in terms of hybridity, resistance (four) and impact resistance. . + A, relative to this, is a liquid hexafluoroselic acid N' hexanide which is not good antistatic in the initial stage of clothing, but it is used. 60t ^ 70〇/〇T^f 6 The surface resistance value after the separation film becomes "lower than the initial value": above: it is confirmed that the antistatic property is degraded in the long-term storage, and the amount is changed by the same ionic solid 3 = 32〇56〇41 200920811 3. Comparing the results of Comparative Example 2 and Comparative Example 3, it can be seen that although the amount of the ionic solid is 100 parts per 100% of the stone olefin resin, the amount of the ionic solid is The effect of the antistatic property is not sufficient. In addition, when I becomes 10 parts of Jing Yitian I, the durability is insufficient. τ [Industrial Applicability] Adhesive of the present invention The resin film of the agent can effectively suppress the electrification of the light material. Moreover, the antistatic property of the light-keeping period can be maintained for a long period of time after the production. The tree that adheres to the first time is, for example, the optical raft. Forming a resin film and obtaining a light that is not used by the liquid crystal by laminating on the glass substrate of the liquid crystal cell In the case of moist heat, the optical layered body absorbs/buffers the stress caused by the dimensional change of the optical film and the glass substrate by the adhesive layer, thereby reducing local stress concentration and suppressing The adhesion or peeling of the adhesive layer to the glass substrate, etc. At the same time, since the optical defects caused by the uneven stress distribution can be prevented, the white color is formed. Further, once the resin film with the adhesive is laminated on the glass If there is any unreasonable situation, even if the resin film and the adhesive are peeled from the glass plate, the surface of the glass substrate will rarely be sticky or smashed, and it can be used as a glass substrate again. In addition, the resin film with an adhesive can also be used as a surface protective film which is bonded to the surface of the optical film and protects the surface until use. An excellent antistatic effect can be imparted, for example, by adhering the optical film to the liquid crystal cell 320560 42 200920811 via an adhesive layer on the opposite side of the surface protective film, and protecting the surface When peeling, the generated static electricity can be changed: The resin film with an adhesive of the present invention can maintain the antistatic property for a long period of time while imparting high antistatic property, and also has excellent durability. The resin film with an adhesive is composed of an optical film to form a resin film, and can be applied to a liquid crystal display device. Further, the resin film with an adhesive can be suitably used as a surface protective film for protecting the surface of the optical film. Description] Μ [Main component symbol description] 320560 43

Claims (1)

200920811 十、申請專利範圍: : 種^έ著刮之樹脂膜’其係在樹脂膜之至少單面上形 , , ν 、 '&quot;站者劑層係由含有下述(Α)成分及(Β) 成为之組成物所形成: 、’、自下式⑴所示之(甲基)丙稀酸酯的結構單 元作為主成分的丙烯酸系樹脂1〇〇重量份, 構早 Ri CH^4 〜2 (I) 〇 (式中,&amp;表示氫原子或甲基鳴表示分別可經碳數i 至1〇之烧氧基所取代之碳數1至Η的烧基或芳炫基); 以及 人此⑻具有有機陽離子且在室溫中為固體的離子性化 &amp;物0.2至8重量份。 2·.如申請專利範圍第β之附黏著劑之樹脂膜,計,相- 對於丙稀酸系樹月旨⑷100重量份,離子性化合物⑻係 以0.2至3重量份之比率存在。 ^申請專利範圍第人或2項之附黏著劑之樹脂膜,其 ’樹脂膜係包含選自偏光臈及相位差膜之膜的光學 膜。 4·如申請專利範圍第1《2項之附黎著劑之樹脂膜,其 中,樹脂膜係表面保護膜。 5.如=請專利範圍第!項之附黏著劑之樹脂膜,其中,在 黏著劑層之表面貼著剝離膜。 320560 44 200920811 • 6. —種光學積層體,係將申請專利範圍第3項之附黏著劑 - 之樹脂膜以其黏著劑層側積層於玻璃基板而形成。 f200920811 X. Patent application scope: : The resin film of the scratched film is formed on at least one side of the resin film, and the ν, '&quot; station layer consists of the following (Α) components and Β) The composition is formed as: , ', from the structural unit of (meth) acrylate represented by the following formula (1), the acrylic resin as a main component, 1 part by weight, and the structure is early Ri CH^4~ 2 (I) 〇 (wherein &amp; represents a hydrogen atom or a methyl group indicating a carbon number of 1 to fluorene or an aryl group which may be substituted by an alkoxy group having a carbon number i to 1 Å, respectively); The person (8) has an organic cation and is 0.2 to 8 parts by weight of an ionization &amp; 2. The resin film of the adhesive of the invention in the scope of Patent Application No. β, the phase - for the acrylic acid tree (4) 100 parts by weight, the ionic compound (8) is present in a ratio of 0.2 to 3 parts by weight. ^ Patent application No. 2 or a resin film with an adhesive attached thereto, wherein the resin film contains an optical film selected from the group consisting of a polarizing film and a film of a retardation film. 4. For example, in the patent application, the resin film of the second coating of the second item is a resin film surface protective film. 5. If = please patent scope! A resin film to which an adhesive is attached, wherein a release film is adhered to the surface of the adhesive layer. 320560 44 200920811 • 6. An optical laminate formed by laminating a resin film attached to the third aspect of the patent application with a layer of an adhesive layer on a glass substrate. f 45 320560 200920811 七、指定代表圖:本案無圖式 &quot; (一)本案指定代表圖為:第()圖。 (二)本代表圖之元件符號簡單說明: 八、本案若有化學式時,請揭示最能顯示發明特徵的化學式: ch245 320560 200920811 VII. Designated representative map: There is no schema in this case &quot; (1) The representative representative map of this case is: (). (2) A brief description of the symbol of the representative figure: 8. If there is a chemical formula in this case, please disclose the chemical formula that best shows the characteristics of the invention: ch2 J1 一C 一C—0—R〇 II 〇J1 - C - C - 0 - R 〇 II 〇 5 3205605 320560
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Families Citing this family (70)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP4963485B2 (en) * 2008-04-07 2012-06-27 綜研化学株式会社 Adhesive composition for polarizing plate and method for producing the same
JP5322280B2 (en) * 2009-03-27 2013-10-23 サイデン化学株式会社 Optical pressure-sensitive adhesive composition
JP2011006595A (en) * 2009-06-26 2011-01-13 Tokyo Ohka Kogyo Co Ltd Adhesive composition and adhesive film
JP5549357B2 (en) * 2009-10-07 2014-07-16 住友化学株式会社 LCD panel
JP5540863B2 (en) * 2010-04-22 2014-07-02 住友化学株式会社 RESIN FILM WITH ADHESIVE AND OPTICAL LAMINATE USING THE SAME
US9429685B2 (en) 2010-05-25 2016-08-30 Sharp Kabushiki Kaisha Laminate
JP5968587B2 (en) 2010-10-21 2016-08-10 日東電工株式会社 Optical adhesive sheet, optical film and display device
KR101784825B1 (en) * 2011-04-21 2017-10-13 동우 화인켐 주식회사 Adhesive composition, polarizing plate and liquid crystal display device comprising the same
JP5921641B2 (en) * 2011-05-26 2016-05-24 日東電工株式会社 Polarizing film with adhesive layer and image display device
JP2013008019A (en) 2011-05-26 2013-01-10 Nitto Denko Corp Polarization film having adhesive layer and image display unit
JP5734754B2 (en) * 2011-06-10 2015-06-17 藤森工業株式会社 Adhesive composition containing antistatic agent and adhesive film
CN104105769B (en) * 2012-02-10 2016-06-15 住友化学株式会社 The manufacture method of the blooming of adhesive sheet, band tackiness agent, optical laminate and adhesive sheet
JP2013163783A (en) * 2012-02-13 2013-08-22 Fujimori Kogyo Co Ltd Adhesive composition, adhesive film and surface-protecting film
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JP2020012098A (en) * 2018-07-10 2020-01-23 三菱ケミカル株式会社 Adhesive composition, and adhesive including the same, adhesive for polarizing plate, and image display device
KR102152295B1 (en) * 2018-09-04 2020-09-04 (주)이녹스첨단소재 Adhesive sheet for display and display comprising the same
JP6734335B2 (en) * 2018-09-20 2020-08-05 藤森工業株式会社 Surface protection film
JP6864031B2 (en) * 2019-04-26 2021-04-21 藤森工業株式会社 Surface protective film
JP6876751B2 (en) * 2019-07-10 2021-05-26 藤森工業株式会社 Surface protective film
KR20210098188A (en) * 2020-01-31 2021-08-10 (주)이녹스첨단소재 Adhesive Sheet for protect display
JP6871450B2 (en) * 2020-03-12 2021-05-12 藤森工業株式会社 Adhesive composition and surface protective film
JP6999735B2 (en) * 2020-04-14 2022-02-10 藤森工業株式会社 Surface protective film
JP7227340B2 (en) * 2020-04-14 2023-02-21 藤森工業株式会社 surface protection film
KR20230004816A (en) * 2020-07-15 2023-01-06 케이와 인코포레이티드 protective sheet and laminate
JP7014879B2 (en) * 2020-11-12 2022-02-01 藤森工業株式会社 Adhesive composition and adhesive film
CN113980171B (en) * 2021-12-01 2022-10-11 香港中文大学(深圳) Polymer material hardened in wet and preparation method and application thereof
JP2023146369A (en) * 2022-03-29 2023-10-12 日東電工株式会社 Optical pressure sensitive adhesive sheet
JP2023146370A (en) * 2022-03-29 2023-10-12 日東電工株式会社 Optical pressure sensitive adhesive sheet

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP4370888B2 (en) * 2002-11-25 2009-11-25 住友化学株式会社 Optical film with adhesive and optical laminate using the same
TW200420703A (en) * 2002-11-25 2004-10-16 Sumitomo Chemical Co Acrylic resin composition, adhesive comprising the composition, and optical laminate comprising the adhesive
JP5030251B2 (en) * 2004-07-26 2012-09-19 日東電工株式会社 Adhesive composition, adhesive sheet and surface protective film
TWI387629B (en) * 2004-07-26 2013-03-01 Nitto Denko Corp Pressure-sensitive adhesive composition, pressure-sensitive adhesive sheets, and surface protecting film
EP1802724B1 (en) * 2004-10-21 2009-04-29 LG Chem, Ltd. Acrylic pressure sensitive adhesive with good antistatic property
WO2006137559A1 (en) * 2005-06-24 2006-12-28 Toyo Ink Manufacturing Co., Ltd. Antistatic acrylic pressure-sensitive adhesive
JP5452850B2 (en) * 2007-07-13 2014-03-26 チェイル インダストリーズ インコーポレイテッド Surface protection sheet for optical members

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