TWI818233B - Transparent double-sided adhesive sheet and adhesive sheet laminate - Google Patents

Transparent double-sided adhesive sheet and adhesive sheet laminate Download PDF

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TWI818233B
TWI818233B TW110104305A TW110104305A TWI818233B TW I818233 B TWI818233 B TW I818233B TW 110104305 A TW110104305 A TW 110104305A TW 110104305 A TW110104305 A TW 110104305A TW I818233 B TWI818233 B TW I818233B
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adhesive sheet
meth
image display
acrylate
display device
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TW110104305A
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Chinese (zh)
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TW202120644A (en
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新美可保留
福田晋也
稲永誠
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日商三菱化學股份有限公司
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Priority claimed from JP2016057812A external-priority patent/JP6558287B2/en
Priority claimed from JP2016227505A external-priority patent/JP7197255B2/en
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    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J11/00—Features of adhesives not provided for in group C09J9/00, e.g. additives
    • C09J11/02—Non-macromolecular additives
    • C09J11/06—Non-macromolecular additives organic
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J4/00—Adhesives based on organic non-macromolecular compounds having at least one polymerisable carbon-to-carbon unsaturated bond ; adhesives, based on monomers of macromolecular compounds of groups C09J183/00 - C09J183/16
    • C09J4/06—Organic non-macromolecular compounds having at least one polymerisable carbon-to-carbon unsaturated bond in combination with a macromolecular compound other than an unsaturated polymer of groups C09J159/00 - C09J187/00
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J133/00—Adhesives 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
    • C09J133/04—Homopolymers or copolymers of esters
    • C09J133/06—Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, the oxygen atom being present only as part of the carboxyl radical
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J7/00—Adhesives in the form of films or foils
    • C09J7/10—Adhesives in the form of films or foils without carriers
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J7/00—Adhesives in the form of films or foils
    • C09J7/30—Adhesives in the form of films or foils characterised by the adhesive composition
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J7/00—Adhesives in the form of films or foils
    • C09J7/40—Adhesives in the form of films or foils characterised by release liners
    • G—PHYSICS
    • G06—COMPUTING; CALCULATING OR COUNTING
    • G06F—ELECTRIC DIGITAL DATA PROCESSING
    • G06F3/00—Input arrangements for transferring data to be processed into a form capable of being handled by the computer; Output arrangements for transferring data from processing unit to output unit, e.g. interface arrangements
    • G06F3/01—Input arrangements or combined input and output arrangements for interaction between user and computer
    • G06F3/03—Arrangements for converting the position or the displacement of a member into a coded form
    • G06F3/041—Digitisers, e.g. for touch screens or touch pads, characterised by the transducing means
    • G—PHYSICS
    • G06—COMPUTING; CALCULATING OR COUNTING
    • G06F—ELECTRIC DIGITAL DATA PROCESSING
    • G06F3/00—Input arrangements for transferring data to be processed into a form capable of being handled by the computer; Output arrangements for transferring data from processing unit to output unit, e.g. interface arrangements
    • G06F3/01—Input arrangements or combined input and output arrangements for interaction between user and computer
    • G06F3/03—Arrangements for converting the position or the displacement of a member into a coded form
    • G06F3/041—Digitisers, e.g. for touch screens or touch pads, characterised by the transducing means
    • G06F3/0412—Digitisers structurally integrated in a display
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J2203/00—Applications of adhesives in processes or use of adhesives in the form of films or foils
    • C09J2203/318—Applications of adhesives in processes or use of adhesives in the form of films or foils for the production of liquid crystal displays
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J2301/00—Additional features of adhesives in the form of films or foils
    • C09J2301/10—Additional features of adhesives in the form of films or foils characterized by the structural features of the adhesive tape or sheet
    • C09J2301/12—Additional features of adhesives in the form of films or foils characterized by the structural features of the adhesive tape or sheet by the arrangement of layers
    • C09J2301/124—Additional features of adhesives in the form of films or foils characterized by the structural features of the adhesive tape or sheet by the arrangement of layers the adhesive layer being present on both sides of the carrier, e.g. double-sided adhesive tape
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J2301/00—Additional features of adhesives in the form of films or foils
    • C09J2301/30—Additional features of adhesives in the form of films or foils characterized by the chemical, physicochemical or physical properties of the adhesive or the carrier
    • C09J2301/312—Additional features of adhesives in the form of films or foils characterized by the chemical, physicochemical or physical properties of the adhesive or the carrier parameters being the characterizing feature

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  • Engineering & Computer Science (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • General Engineering & Computer Science (AREA)
  • Theoretical Computer Science (AREA)
  • Human Computer Interaction (AREA)
  • Physics & Mathematics (AREA)
  • General Physics & Mathematics (AREA)
  • Adhesive Tapes (AREA)
  • Laminated Bodies (AREA)
  • Adhesives Or Adhesive Processes (AREA)

Abstract

本發明提供一種新穎圖像顯示裝置用透明雙面黏著片，其具有紫外線吸收功能，且於使用黏著片進行一次貼附後，可進而硬化而進行二次貼附。 本發明提供一種包含黏著劑樹脂組合物之圖像顯示裝置用透明雙面黏著片，該黏著劑樹脂組合物含有(甲基)丙烯酸系共聚物(A)、交聯劑(B)、波長405 nm下之吸光係數為10 mL/(g∙cm)以上之光聚合起始劑(C)及紫外線吸收劑(D)。The present invention provides a novel transparent double-sided adhesive sheet for image display devices, which has ultraviolet absorption function and can be further hardened for secondary attachment after the adhesive sheet is used for primary attachment. The invention provides a transparent double-sided adhesive sheet for image display devices containing an adhesive resin composition. The adhesive resin composition contains a (meth)acrylic copolymer (A), a cross-linking agent (B), and a wavelength 405 Photopolymerization initiator (C) and ultraviolet absorber (D) whose absorption coefficient at nm is 10 mL/(g∙cm) or above.

Description

透明雙面黏著片及黏著片積層體Transparent double-sided adhesive sheet and adhesive sheet laminate

本發明係關於一種可作為用以構成如例如個人電腦、移動終端(PDA)、遊戲機、電視(TV)、汽車導航、觸控面板、手寫板等之圖像顯示裝置之構件而使用的透明雙面黏著片。The present invention relates to a transparent material that can be used as a component of an image display device such as a personal computer, a mobile terminal (PDA), a game console, a television (TV), a car navigation system, a touch panel, a tablet, etc. Double-sided adhesive sheet.

近年來，為了提高圖像顯示裝置之視認性，進行有藉由利用接著劑將液晶顯示器(LCD)、電漿顯示器(PDP)、電致發光顯示器(ELD)等圖像顯示面板與配置於其前表面側(視認側)之保護面板或觸控面板構件之間之空隙予以填充，而抑制入射光或自顯示圖像之出射光於空氣層界面之反射。 作為利用黏著劑將此種圖像顯示裝置用構成構件間之空隙予以填充之方法，已知有於將含有紫外線硬化性樹脂之液狀接著樹脂組合物填充至該空隙後，照射紫外線使其硬化之方法(專利文獻1)。 又，亦已知有使用黏著片將圖像顯示裝置用構成構件間之空隙予以填充之方法。例如於專利文獻2中，揭示有於將藉由紫外線進行1次交聯之黏著片貼附於圖像顯示裝置構成構件後，隔著圖像顯示裝置構成構件對黏著片照射紫外線而使其2次硬化之方法。 於專利文獻3中，揭示有使用包含以重量平均分子量為2萬至10萬之(甲基)丙烯酸胺基甲酸酯作為主成分之25℃下之損耗正切未達1之熱熔型接著組合物的黏著片，將圖像顯示裝置用構成構件間之空隙予以填充之方法。 先前技術文獻 專利文獻 專利文獻1：國際公開2010/027041號公報 專利文獻2：日本專利第4971529號公報 專利文獻3：國際公開2010/038366號公報In recent years, in order to improve the visibility of image display devices, image display panels such as liquid crystal displays (LCDs), plasma displays (PDP), and electroluminescent displays (ELD) have been disposed on them by using adhesives. The gaps between the protective panel or touch panel components on the front surface side (viewing side) are filled to suppress the reflection of incident light or light emitted from the displayed image at the air layer interface. As a method of filling the gaps between the constituent members of such an image display device with an adhesive, it is known to fill the gaps with a liquid adhesive resin composition containing an ultraviolet curable resin and then irradiate ultraviolet rays to cure them. method (Patent Document 1). Also known is a method of filling gaps between components of an image display device using an adhesive sheet. For example, Patent Document 2 discloses that after affixing an adhesive sheet that is primarily cross-linked by ultraviolet rays to a component of an image display device, the adhesive sheet is irradiated with ultraviolet rays through the component of the image display device to cause it to become 2 Secondary hardening method. Patent Document 3 discloses the use of a hot-melt adhesive combination containing (meth)acrylic urethane with a weight average molecular weight of 20,000 to 100,000 as a main component and a loss tangent of less than 1 at 25°C. It is a method of filling the gaps between the components of an image display device with an adhesive sheet. Prior technical literature patent documents Patent Document 1: International Publication No. 2010/027041 Patent Document 2: Japanese Patent No. 4971529 Patent Document 3: International Publication No. 2010/038366

[發明所欲解決之問題] 且說，於使用包含含有基礎樹脂、交聯劑及紫外線聚合起始劑之黏著劑樹脂組合物之黏著片，貼附2個圖像顯示裝置構成構件之情形時，經由該黏著片將2個圖像顯示裝置構成構件一次貼附後，自一圖像顯示裝置構成構件之外側照射紫外線，透過該圖像顯示裝置構成構件將該黏著片進行紫外線硬化而進行二次貼附，根據如上方法，可填充被黏著面之凹凸且一次貼附，並且最終使其硬化而可進一步提高接著可靠性。 然而，該具有紫外線感應性之黏著片若長時間暴露於紫外線中，則黏著片自身會逐漸劣化，有產生分解物而產生發泡或剝離之可能性。 又，由於圖像顯示裝置構成構件中存在容易紫外線劣化之構件，故而於此種情形時，無法藉由如上所述之方法將2個圖像顯示裝置構成構件貼附。 進而，於圖像顯示裝置構成構件具有紫外線吸收性之情形時，即便隔著該構件照射紫外線，紫外線亦無法充分到達至黏著片，因此於此種情形時，無法藉由如上所述之方法將2個圖像顯示裝置構成構件貼附。 另一方面，隨著圖像顯示裝置之薄壁化進展，而逐漸對黏著片要求新的功能。為了防止液晶或有機EL元件、偏光板等之紫外線劣化，有要求圖像顯示裝置構成構件具備紫外線吸收功能之情況，紫外線吸收功能一般由偏光板保護膜承擔。然而，隨著圖像顯示裝置構成構件之薄壁化，偏光板保護膜之薄壁化亦進展，而難以獲得充分之紫外線吸收功能。因此，對偏光板保護膜以外之圖像顯示裝置構成構件、例如黏著劑或黏著片亦要求具備紫外線吸收功能。 然而，難以對如上所述之紫外線硬化型黏著片賦予紫外線吸收功能。另一方面，若不採用於使用黏著片填充被黏著面之凹凸且一次貼附後，進而使其硬化而進行二次貼附之方法，則存在如下問題：無法兼顧於貼合構件之被黏著面具有凹凸之情形時之階差吸收性與貼合後之耐發泡可靠性。 因此，本發明提供一種新穎之透明雙面黏著片，其具有紫外線吸收功能，並且於使用黏著片進行一次貼附後，可進而使其硬化而進行二次貼附。 [解決問題之技術手段] 本發明係包含含有(甲基)丙烯酸系共聚物(A)、交聯劑(B)、波長405 nm下之吸光係數為10 mL/(g∙cm)以上之光聚合起始劑(C)及紫外線吸收劑(D)之黏著劑樹脂組合物的透明雙面黏著片。 [發明之效果] 本發明之圖像顯示用透明雙面黏著片具有紫外線吸收功能，並且於使用黏著片進行一次貼附後，可進而使其光硬化而進行二次貼附，因此可兼顧於貼合構件之被黏著面具有凹凸之情形時之階差吸收性與貼合後之耐發泡可靠性。[Problem to be solved by the invention] In addition, when two image display device components are attached using an adhesive sheet containing an adhesive resin composition containing a base resin, a cross-linking agent, and an ultraviolet polymerization initiator, the two images are attached via the adhesive sheet. After the components of the image display device are attached once, ultraviolet rays are irradiated from the outside of the component of the image display device, and the adhesive sheet is cured by ultraviolet rays through the component of the image display device and then attached a second time. According to the above method, it can be Filling the unevenness of the adhered surface and attaching it once, and finally hardening it can further improve the bonding reliability. However, if the ultraviolet-sensitive adhesive sheet is exposed to ultraviolet light for a long time, the adhesive sheet itself will gradually deteriorate and may produce decomposition products, leading to foaming or peeling. Furthermore, since there are components that are easily degraded by ultraviolet rays among the components of the image display device, in this case, it is impossible to attach the two components of the image display device by the method described above. Furthermore, when the components of the image display device have ultraviolet absorptivity, even if ultraviolet rays are irradiated through the components, the ultraviolet rays cannot sufficiently reach the adhesive sheet. Therefore, in this case, it is impossible to use the above method to remove the ultraviolet rays. Two image display device components are attached. On the other hand, as image display devices become thinner, new functions are gradually required for the adhesive sheet. In order to prevent ultraviolet degradation of liquid crystal or organic EL elements, polarizing plates, etc., components of image display devices are sometimes required to have ultraviolet absorbing functions. The ultraviolet absorbing function is generally performed by polarizing plate protective films. However, as components of image display devices become thinner, the thickness of polarizing plate protective films also progresses, making it difficult to obtain sufficient ultraviolet absorption function. Therefore, components of the image display device other than the polarizing plate protective film, such as adhesives or adhesive sheets, are also required to have ultraviolet absorbing functions. However, it is difficult to provide an ultraviolet absorbing function to the ultraviolet curable adhesive sheet as described above. On the other hand, if the method of using an adhesive sheet to fill the unevenness of the adhered surface and attaching it once, then hardening it and attaching it a second time is not adopted, there will be the following problem: it is impossible to take into account the adhesion of the bonded member. The step absorption ability when the surface has uneven surface and the foaming resistance reliability after bonding. Therefore, the present invention provides a novel transparent double-sided adhesive sheet, which has ultraviolet absorption function, and after the adhesive sheet is used for primary attachment, it can be further hardened for secondary attachment. [Technical means to solve problems] The present invention contains a (meth)acrylic copolymer (A), a cross-linking agent (B), and a photopolymerization initiator (C) with an absorption coefficient of 10 mL/(g∙cm) or more at a wavelength of 405 nm. A transparent double-sided adhesive sheet composed of an adhesive resin composition of ultraviolet absorber (D). [Effects of the invention] The transparent double-sided adhesive sheet for image display of the present invention has ultraviolet absorption function, and after the adhesive sheet is used for primary attachment, it can be further photo-hardened for secondary attachment, so it can be used as a bonding component. The step absorption ability when the adhesive surface is uneven and the foaming resistance reliability after bonding.

以下，對本發明之實施形態之一例進行詳細說明。但是，本案發明並不限定於下述實施形態。 ＜本黏著片＞ 本發明之實施形態之一例之透明雙面黏著片係包含含有(甲基)丙烯酸系共聚物(A)、交聯劑(B)、波長405 nm下之吸光係數為10 mL/(g∙cm)以上之光聚合起始劑(C)及紫外線吸收劑(D)之黏著劑樹脂組合物(稱為「本黏著劑組合物」)的透明雙面黏著片(稱為「本黏著片」)。 [(甲基)丙烯酸系共聚物(A)] 作為本黏著片之基礎聚合物之(甲基)丙烯酸系聚合物可藉由為了使其聚合而使用之丙烯酸系單體或甲基丙烯酸系單體之種類、組成比率、進而聚合條件等，而適當調整玻璃轉移溫度(Tg)等特性。 本黏著片中之所謂「基礎聚合物」係指作為本黏著片之主成分之樹脂。並非規定具體含量。作為標準，為佔據本黏著片中所含之樹脂之50質量%以上、尤其65質量%以上、尤其80質量%以上(包含100質量%)質量%以上之樹脂。再者，於基礎聚合物為兩種以上之情形時，其等之合計量相當於上述含量。 作為(甲基)丙烯酸系(共)聚合物(A)，例如除(甲基)丙烯酸烷基酯之均聚物以外，可列舉藉由使其與具有共聚性之單體成分進行聚合而獲得之共聚物，更佳為可列舉含有(甲基)丙烯酸烷基酯、及選自可與其共聚之含羧基單體、含羥基單體、含胺基單體、含環氧基單體、含醯胺基單體等乙烯基單體中之任一種以上之單體作為單體成分之共聚物。 更具體而言，可列舉包含選自側鏈之碳數4～18之直鏈或支鏈(甲基)丙烯酸烷基酯(以下亦稱為「共聚性單體A」)、可與其共聚之含羧基單體(以下亦稱為「共聚性單體B」)、乙烯基單體(以下亦稱為「共聚性單體C」)、側鏈之碳數為1～3之(甲基)丙烯酸酯(以下亦稱為「共聚性單體D」)、及含羥基單體(以下稱為「共聚性單體E」)中之任一種以上之單體之共聚物。 又，作為尤佳之例示，亦可列舉：(a)包含含有共聚性單體A以及共聚性單體B及/或共聚性單體C之單體成分之共聚物、或(b)包含含有共聚性單體A、共聚性單體B及/或共聚性單體C、以及共聚性單體D及/或共聚性單體E之單體成分之共聚物。具體而言，可列舉：共聚性單體A及B之共聚物、共聚性單體A及C之共聚物、共聚性單體A、B及C之共聚物、共聚性單體A、B及D之共聚物、共聚性單體A、B及E之共聚物、共聚性單體A、B、D及E之共聚物、共聚性單體A、C及D之共聚物、共聚性單體A、C及E之共聚物、共聚性單體A、C、D及E之共聚物、共聚性單體A、B、C及D之共聚物、共聚性單體A、B、C及E之共聚物、共聚性單體A、B、C、D及E之共聚物。 作為上述「共聚性單體A」，例如可列舉：(甲基)丙烯酸正丁酯、(甲基)丙烯酸異丁酯、(甲基)丙烯酸第二丁酯、(甲基)丙烯酸第三丁酯、(甲基)丙烯酸戊酯、(甲基)丙烯酸異戊酯、(甲基)丙烯酸新戊酯、(甲基)丙烯酸己酯、(甲基)丙烯酸環己酯、(甲基)丙烯酸庚酯、(甲基)丙烯酸2-乙基己酯、(甲基)丙烯酸正辛酯、(甲基)丙烯酸異辛酯、(甲基)丙烯酸壬酯、(甲基)丙烯酸異壬酯、(甲基)丙烯酸第三丁基環己酯、(甲基)丙烯酸癸酯、(甲基)丙烯酸異癸酯、(甲基)丙烯酸十一烷基酯、(甲基)丙烯酸月桂酯、(甲基)丙烯酸十三烷基酯、(甲基)丙烯酸十四烷基酯、(甲基)丙烯酸鯨蠟酯、(甲基)丙烯酸硬脂酯、(甲基)丙烯酸異硬脂酯、(甲基)丙烯酸異𦯉酯、3,5,5-三甲基環己烷(甲基)丙烯酸酯、(甲基)丙烯酸二環戊酯、(甲基)丙烯酸二環戊烯酯、(甲基)丙烯酸二環戊烯氧基乙酯等。該等亦可使用1種或組合2種以上而使用。 上述共聚性單體A較佳為於共聚物之所有單體成分中含有30質量%以上且90質量%以下，其中進而較佳為以35質量%以上或88質量%以下之範圍含有，其中尤其進而較佳為以40質量%以上或85質量%以下之範圍含有。 作為上述「共聚性單體B」，例如可列舉：(甲基)丙烯酸、2-(甲基)丙烯醯氧基乙基六氫苯二甲酸、2-(甲基)丙烯醯氧基丙基六氫苯二甲酸、2-(甲基)丙烯醯氧基乙基苯二甲酸、2-(甲基)丙烯醯氧基丙基苯二甲酸、2-(甲基)丙烯醯氧基乙基順丁烯二酸、2-(甲基)丙烯醯氧基丙基順丁烯二酸、2-(甲基)丙烯醯氧基乙基琥珀酸、2-(甲基)丙烯醯氧基丙基琥珀酸、丁烯酸、反丁烯二酸、順丁烯二酸、伊康酸。該等亦可使用1種或組合2種以上。再者，「(甲基)丙烯酸」之含義包括丙烯酸及甲基丙烯酸。同樣，「(甲基)丙烯醯基」之含義包括丙烯醯基及甲基丙烯醯基。 作為上述「共聚性單體C」，可列舉於分子內具有乙烯基之化合物。作為此種化合物，可例示：烷基之碳數為1～12之(甲基)丙烯酸烷基酯類；以及於分子內具有羥基、醯胺基及烷氧基烷基等官能基之官能性單體類；以及聚伸烷基二醇二(甲基)丙烯酸酯類；以及乙酸乙烯酯、丙酸乙烯酯及月桂酸乙烯酯等乙烯酯單體；以及苯乙烯、氯苯乙烯、氯甲基苯乙烯、α-甲基苯乙烯及其他取代苯乙烯等芳香族乙烯基單體。該等亦可使用1種或組合2種以上。 上述共聚性單體B及上述共聚性單體C較佳為於共聚物之所有單體成分中以1.2質量%～15質量%以下之範圍含有，其中就獲得優異之黏著物性之觀點而言，較佳為以1.5質量%以上或10質量%以下之範圍含有，其中尤佳為以2質量%以上或8質量%以下之範圍含有。 作為上述「共聚性單體D」，可列舉：(甲基)丙烯酸甲酯、(甲基)丙烯酸乙酯、(甲基)丙烯酸正丙酯、(甲基)丙烯酸異丙酯等。該等亦可使用1種或組合2種以上。 上述共聚性單體D較佳為於共聚物之所有單體成分中含有0質量%以上且70質量%以下，其中進而較佳為以3質量%以上或65質量%以下之範圍含有，其中尤其進而較佳為以5質量%以上或60質量%以下之範圍含有。 作為上述「共聚性單體E」，可列舉：(甲基)丙烯酸2-羥基乙酯、(甲基)丙烯酸2-羥基丙酯、(甲基)丙烯酸3-羥基丙酯、(甲基)丙烯酸2-羥基丁酯等(甲基)丙烯酸羥基烷基酯類。該等亦可使用1種或組合2種以上。 上述共聚性單體E較佳為於共聚物之所有單體成分中含有0質量%以上且30質量%以下，其中進而較佳為以0質量%以上或25質量%以下之範圍含有，其中尤其進而較佳為以0質量%以上或20質量%以下之範圍含有。 除了上述揭示者以外，亦可視需要適當使用順丁烯二酸酐、伊康酸酐等含酸酐基單體，(甲基)丙烯酸縮水甘油酯、α-乙基丙烯酸縮水甘油酯，(甲基)丙烯酸3,4-環氧丁酯等含環氧基單體，(甲基)丙烯酸二甲基胺基乙酯、(甲基)丙烯酸二乙基胺基乙酯等含胺基之(甲基)丙烯酸酯系單體，(甲基)丙烯醯胺、N-第三丁基(甲基)丙烯醯胺、N-羥甲基(甲基)丙烯醯胺、N-甲氧基甲基(甲基)丙烯醯胺、N-丁氧基甲基(甲基)丙烯醯胺、雙丙酮(甲基)丙烯醯胺、順丁烯二醯胺、順丁烯二醯亞胺等含有醯胺基之單體，乙烯基吡咯啶酮、乙烯基吡啶、乙烯基咔唑等雜環系鹼性單體等。 作為(甲基)丙烯酸系(共)聚合物之具體例，例如可列舉：使(甲基)丙烯酸2-乙基己酯、(甲基)丙烯酸辛酯、(甲基)丙烯酸癸酯、(甲基)丙烯酸月桂酯、(甲基)丙烯酸異硬脂酯、(甲基)丙烯酸丁酯、(甲基)丙烯酸乙酯、(甲基)丙烯酸甲酯等單體成分(a)，具有羧基之(甲基)丙烯酸、2-(甲基)丙烯醯氧基乙基六氫苯二甲酸、2-(甲基)丙烯醯氧基丙基六氫苯二甲酸、2-(甲基)丙烯醯氧基乙基苯二甲酸、2-(甲基)丙烯醯氧基丙基苯二甲酸、2-(甲基)丙烯醯氧基乙基順丁烯二酸、2-(甲基)丙烯醯氧基丙基順丁烯二酸、2-(甲基)丙烯醯氧基乙基琥珀酸、2-(甲基)丙烯醯氧基丙基琥珀酸、丁烯酸、反丁烯二酸、順丁烯二酸、伊康酸等單體成分(b)，及具有有機官能基等之(甲基)丙烯酸羥基乙酯、(甲基)丙烯酸羥基丙酯、(甲基)丙烯酸羥基丁酯、(甲基)丙烯酸甘油酯、順丁烯二酸單甲酯、伊康酸單甲酯、乙酸乙烯酯、(甲基)丙烯酸縮水甘油酯、(甲基)丙烯醯胺、(甲基)丙烯腈、氟化(甲基)丙烯酸酯、(甲基)丙烯酸聚矽氧酯等單體成分(c)進行共聚而獲得之(甲基)丙烯酸酯共聚物。 (甲基)丙烯酸系(共)聚合物之質量平均分子量較佳為10萬～150萬，其中較佳為15萬以上或130萬以下，其中尤佳為20萬以上或120萬以下。 於欲獲得凝聚力較高之黏著組合物之情形時，就分子量越大，越可藉由分子鏈之纏結而獲得凝聚力之觀點而言，質量平均分子量較佳為70萬～150萬，尤佳為80萬以上或130萬以下。另一方面，於欲獲得流動性或應力緩和性較高之黏著組合物之情形時，質量平均分子量較佳為7萬～70萬，尤佳為10萬以上或60萬以下。又，於成形黏著片等時不使用溶劑之情形時，難以使用分子量較大之聚合物，因此丙烯酸系共聚物之質量平均分子量較佳為7萬～70萬，尤佳為10萬以上或60萬以下，其中尤佳為15萬以上或50萬以下。 (丙烯酸系共聚物(A1)) 作為本黏著片之較佳之基礎聚合物之一例，可列舉包含具備巨分子單體作為枝成分之接枝共聚物之(甲基)丙烯酸系共聚物(A1)。 只要將上述丙烯酸系共聚物(A1)作為基礎樹脂構成本黏著片，則本黏著片可於室溫狀態下保持片狀並且顯示自黏性，若於未交聯狀態下加熱，則具有熔融或流動之熱熔性，可進而使其光硬化，可於光硬化後發揮優異之凝聚力而進行接著。 由此，只要使用丙烯酸系共聚物(A1)作為本黏著片之基礎聚合物，則即便為未交聯狀態，亦可具備如下性質，即，於室溫(20℃)下顯示黏著性，且於100℃下軟化或流體化之性質，或加熱至50～90℃、更佳為60℃以上或80℃以下之溫度時軟化或流體化之性質。 構成上述丙烯酸系共聚物(A1)之幹成分之共聚物之玻璃轉移溫度較佳為-70～0℃。 此時，所謂構成幹成分之共聚物成分之玻璃轉移溫度，係指僅使組成丙烯酸系共聚物(A1)之幹成分之單體成分共聚而獲得之聚合物之玻璃轉移溫度。具體而言，意指自該共聚物各成分之均聚物獲得之聚合物之玻璃轉移溫度與構成比率，藉由Fox之計算式而算出之值。 再者，所謂Fox之計算式係指藉由以下之式而求出之計算值，可使用聚合物手冊[Polymer HandBook,J.Brandrup,Interscience,1989]所記載之值而求出。 1/(273＋Tg)＝Σ(Wi/(273＋Tgi)) [式中，Wi表示單體i之重量分率，Tgi表示單體i之均聚物之Tg(℃)] 構成上述丙烯酸系共聚物(A1)之幹成分之共聚物成分之玻璃轉移溫度會對室溫狀態下之本黏著片之柔軟性、或本黏著片對被黏著體之潤濕性、即接著性造成影響，因此為了使本黏著片於室溫狀態下獲得適度之接著性(黏性)，該玻璃轉移溫度較佳為-70℃～0℃，其中尤佳為-65℃以上或-5℃以下，其中尤佳為-60℃以上或-10℃以下。 但，即便該共聚物成分之玻璃轉移溫度設為相同溫度，亦可藉由調整分子量而調整黏彈性。例如可藉由減小共聚物成分之分子量而使其更柔軟化。 作為上述丙烯酸系共聚物(A1)之幹成分含有之(甲基)丙烯酸酯單體，例如可列舉：(甲基)丙烯酸甲酯、(甲基)丙烯酸乙酯、(甲基)丙烯酸丙酯、(甲基)丙烯酸異丙酯、(甲基)丙烯酸正丁酯、(甲基)丙烯酸異丁酯、(甲基)丙烯酸第二丁酯、(甲基)丙烯酸第三丁酯、(甲基)丙烯酸戊酯、(甲基)丙烯酸異戊酯、(甲基)丙烯酸新戊酯、(甲基)丙烯酸己酯、(甲基)丙烯酸環己酯、(甲基)丙烯酸庚酯、(甲基)丙烯酸2-乙基己酯、丙烯酸正辛酯、丙烯酸異辛酯、(甲基)丙烯酸壬酯、(甲基)丙烯酸異壬酯、(甲基)丙烯酸第三丁基環己酯、(甲基)丙烯酸癸酯、(甲基)丙烯酸異癸酯、(甲基)丙烯酸十一烷基酯、(甲基)丙烯酸月桂酯、(甲基)丙烯酸鯨蠟酯、(甲基)丙烯酸硬脂酯、(甲基)丙烯酸異硬脂酯、丙烯酸山崳酯、(甲基)丙烯酸異𦯉酯、(甲基)丙烯酸2-苯氧基乙酯、3,5,5-三甲基環己烷丙烯酸酯、對異丙苯基苯酚EO改性(甲基)丙烯酸酯、(甲基)丙烯酸二環戊酯、(甲基)丙烯酸二環戊烯酯、(甲基)丙烯酸二環戊烯氧基乙酯、(甲基)丙烯酸苄酯等。於該等中，亦可使用具有親水基或有機官能基等之(甲基)丙烯酸羥基乙酯、(甲基)丙烯酸羥基丙酯、(甲基)丙烯酸羥基丁酯、(甲基)丙烯酸甘油酯等含羥基之(甲基)丙烯酸酯，或(甲基)丙烯酸、2-(甲基)丙烯醯氧基乙基六氫苯二甲酸、2-(甲基)丙烯醯氧基丙基六氫苯二甲酸、2-(甲基)丙烯醯氧基乙基苯二甲酸、2-(甲基)丙烯醯氧基丙基苯二甲酸、2-(甲基)丙烯醯氧基乙基順丁烯二酸、2-(甲基)丙烯醯氧基丙基順丁烯二酸、2-(甲基)丙烯醯氧基乙基琥珀酸、2-(甲基)丙烯醯氧基丙基琥珀酸、丁烯酸、反丁烯二酸、順丁烯二酸、伊康酸、順丁烯二酸單甲酯、伊康酸單甲酯等含羧基單體，順丁烯二酸酐、伊康酸酐等含酸酐基單體，(甲基)丙烯酸縮水甘油酯、α-乙基丙烯酸縮水甘油酯、(甲基)丙烯酸3,4-環氧丁酯等含環氧基單體，(甲基)丙烯酸二甲基胺基乙酯、(甲基)丙烯酸二乙基胺基乙酯等含胺基之(甲基)丙烯酸酯系單體，(甲基)丙烯醯胺、N-第三丁基(甲基)丙烯醯胺、N-羥甲基(甲基)丙烯醯胺、N-甲氧基甲基(甲基)丙烯醯胺、N-丁氧基甲基(甲基)丙烯醯胺、雙丙酮丙烯醯胺、順丁烯二醯胺、順丁烯二醯亞胺等含有醯胺基之單體，乙烯基吡咯啶酮、乙烯基吡啶、乙烯基咔唑等雜環系鹼性單體等。 又，亦可適當使用可與上述丙烯酸系單體或甲基丙烯酸系單體進行共聚之苯乙烯、第三丁基苯乙烯、α-甲基苯乙烯、乙烯基甲苯、丙烯腈、甲基丙烯腈、乙酸乙烯酯、丙酸乙烯酯、烷基乙烯醚、羥基烷基乙烯醚、烷基乙烯基單體等各種乙烯基單體。 又，丙烯酸系共聚物(A1)之幹成分較佳為含有疏水性之(甲基)丙烯酸酯單體與親水性之(甲基)丙烯酸酯單體作為結構單元。 若丙烯酸系共聚物(A1)之幹成分僅由疏水性單體構成，則認為有濕熱白化之傾向，因此較佳為將親水性單體亦導入至幹成分而防止濕熱白化。 具體而言，作為上述丙烯酸系共聚物(A1)之幹成分，可列舉疏水性之(甲基)丙烯酸酯單體、親水性之(甲基)丙烯酸酯單體、及巨分子單體之末端之聚合性官能基進行無規共聚而成之共聚物成分。 此處，作為上述疏水性之(甲基)丙烯酸酯單體，例如可列舉：(甲基)丙烯酸正丁酯、(甲基)丙烯酸異丁酯、(甲基)丙烯酸第二丁酯、(甲基)丙烯酸第三丁酯、(甲基)丙烯酸戊酯、(甲基)丙烯酸異戊酯、(甲基)丙烯酸新戊酯、(甲基)丙烯酸己酯、(甲基)丙烯酸環己酯、(甲基)丙烯酸庚酯、(甲基)丙烯酸2-乙基己酯、丙烯酸正辛酯、丙烯酸異辛酯、(甲基)丙烯酸壬酯、(甲基)丙烯酸異壬酯、(甲基)丙烯酸第三丁基環己酯、(甲基)丙烯酸癸酯、(甲基)丙烯酸異癸酯、(甲基)丙烯酸十一烷基酯、(甲基)丙烯酸月桂酯、(甲基)丙烯酸鯨蠟酯、(甲基)丙烯酸硬脂酯、(甲基)丙烯酸異硬脂酯、丙烯酸山崳酯、(甲基)丙烯酸異𦯉酯、(甲基)丙烯酸環己酯、(甲基)丙烯酸二環戊烯氧基乙酯、甲基丙烯酸甲酯。 又，作為疏水性之乙烯基單體，可列舉：乙酸乙烯酯、苯乙烯、第三丁基苯乙烯、α-甲基苯乙烯、乙烯基甲苯、烷基乙烯基單體等。 作為上述親水性之(甲基)丙烯酸酯單體，例如可列舉：丙烯酸甲酯、(甲基)丙烯酸、(甲基)丙烯酸四氫糠酯、或(甲基)丙烯酸羥基乙酯、(甲基)丙烯酸羥基丙酯、(甲基)丙烯酸羥基丁酯、(甲基)丙烯酸甘油酯等含羥基之(甲基)丙烯酸酯、或(甲基)丙烯酸、2-(甲基)丙烯醯氧基乙基六氫苯二甲酸、2-(甲基)丙烯醯氧基丙基六氫苯二甲酸、2-(甲基)丙烯醯氧基乙基苯二甲酸、2-(甲基)丙烯醯氧基丙基苯二甲酸、2-(甲基)丙烯醯氧基乙基順丁烯二酸、2-(甲基)丙烯醯氧基丙基順丁烯二酸、2-(甲基)丙烯醯氧基乙基琥珀酸、2-(甲基)丙烯醯氧基丙基琥珀酸、丁烯酸、反丁烯二酸、順丁烯二酸、伊康酸、順丁烯二酸單甲酯、伊康酸單甲酯等含羧基單體、順丁烯二酸酐、伊康酸酐等含酸酐基單體、(甲基)丙烯酸縮水甘油酯、α-乙基丙烯酸縮水甘油酯、(甲基)丙烯酸3,4-環氧丁酯等含環氧基單體、甲氧基聚乙二醇(甲基)丙烯酸酯等烷氧基聚伸烷基二醇(甲基)丙烯酸酯、N,N-二甲基丙烯醯胺、羥基乙基丙烯醯胺等。 (枝成分：巨分子單體) 丙烯酸系共聚物(A1)較佳為導入巨分子單體作為接枝共聚物之枝成分，而含有源自巨分子單體之重複單元。 所謂巨分子單體係指具有末端之聚合性官能基及高分子量骨架成分之高分子單體。 巨分子單體之玻璃轉移溫度(Tg)較佳為高於構成上述丙烯酸系共聚物(A1)之共聚物成分之玻璃轉移溫度。 具體而言，由於巨分子單體之玻璃轉移溫度(Tg)會對本黏著片之加熱熔融溫度(熱熔溫度)造成影響，故而巨分子單體之玻璃轉移溫度(Tg)較佳為30℃～120℃，其中進而較佳為中40℃以上或110℃以下，其中進而較佳為50℃以上或100℃以下。 只要為此種玻璃轉移溫度(Tg)，則可藉由調整分子量而保持優異之加工性或保管穩定性，並且可調整為於50℃至80℃附近熱熔。 所謂巨分子單體之玻璃轉移溫度係指該巨分子單體本身之玻璃轉移溫度，可藉由示差掃描熱量計(DSC)進行測定。 又，為了使得於室溫狀態下，枝成分彼此相互牽引，作為黏著劑組合物可維持如進行物理交聯之狀態，並且藉由加熱至適度之溫度，上述物理交聯解除而可獲得流動性，亦較佳為調整巨分子單體之分子量或含量。 就該觀點而言，巨分子單體較佳為於丙烯酸系共聚物(A1)中以5質量%～30質量%之比率含有，其中較佳為6質量%以上或25質量%以下，其中較佳為8質量%以上或20質量%以下。 又，巨分子單體之數量平均分子量較佳為500以上且未達8000，其中較佳為800以上或未達7500，其中較佳為1000以上或未達7000。 巨分子單體可適當使用通常製造者(例如東亞合成公司製造之巨分子單體等)。 巨分子單體之高分子量骨架成分較佳為包含丙烯酸系聚合物或乙烯系聚合物。 作為上述巨分子單體之高分子量骨架成分，例如可列舉：(甲基)丙烯酸甲酯、(甲基)丙烯酸乙酯、(甲基)丙烯酸丙酯、(甲基)丙烯酸異丙酯、(甲基)丙烯酸正丁酯、(甲基)丙烯酸異丁酯、(甲基)丙烯酸第二丁酯、(甲基)丙烯酸第三丁酯、(甲基)丙烯酸戊酯、(甲基)丙烯酸異戊酯、(甲基)丙烯酸新戊酯、(甲基)丙烯酸己酯、(甲基)丙烯酸環己酯、(甲基)丙烯酸庚酯、(甲基)丙烯酸2-乙基己酯、丙烯酸正辛酯、丙烯酸異辛酯、(甲基)丙烯酸壬酯、(甲基)丙烯酸異壬酯、(甲基)丙烯酸第三丁基環己酯、(甲基)丙烯酸癸酯、(甲基)丙烯酸異癸酯、(甲基)丙烯酸十一烷基酯、(甲基)丙烯酸月桂酯、(甲基)丙烯酸鯨蠟酯、(甲基)丙烯酸硬脂酯、(甲基)丙烯酸異硬脂酯、丙烯酸山崳酯、(甲基)丙烯酸異𦯉酯、(甲基)丙烯酸2-苯氧基乙酯、3,5,5-三甲基環己烷丙烯酸酯、對異丙苯基苯酚EO改性(甲基)丙烯酸酯、(甲基)丙烯酸二環戊酯、(甲基)丙烯酸二環戊烯酯、(甲基)丙烯酸二環戊烯氧基乙酯、(甲基)丙烯酸苄酯、(甲基)丙烯酸羥基烷基酯、(甲基)丙烯酸、(甲基)丙烯酸縮水甘油酯、(甲基)丙烯醯胺、N,N-二甲基(甲基)丙烯醯胺、(甲基)丙烯腈、(甲基)丙烯酸烷氧基烷基酯、烷氧基聚伸烷基二醇(甲基)丙烯酸酯等(甲基)丙烯酸酯單體、或苯乙烯、第三丁基苯乙烯、α-甲基苯乙烯、乙烯基甲苯、烷基乙烯基單體、烷基乙烯酯、烷基乙烯醚、羥基烷基乙烯醚等各種乙烯基單體，該等可單獨使用或組合兩種以上而使用。 作為上述巨分子單體之末端聚合性官能基，例如可列舉甲基丙烯醯基、丙烯醯基、乙烯基等。 [交聯劑(B)] 作為交聯劑(B)，較佳為至少具有雙鍵交聯之交聯劑。例如可列舉具有選自(甲基)丙烯醯基、環氧基、異氰酸酯基、羧基、羥基、碳二醯亞胺基、㗁唑啉基、氮丙啶基、乙烯基、胺基、亞胺基、醯胺基中之至少1種交聯性官能基之交聯劑，亦可使用1種或組合2種以上而使用。又，亦包含交聯劑(B)與(甲基)丙烯酸系共聚物(A)化學鍵結之態樣。 其中，較佳為使用多官能(甲基)丙烯酸酯。此處，多官能係指具有2個以上之交聯性官能基者。再者，亦可視需要具有3個以上、4個以上之交聯性官能基。 再者，上述交聯性官能基亦可由可去保護之保護基保護。 作為此種多官能(甲基)丙烯酸酯，例如可列舉：1,4-丁二醇二(甲基)丙烯酸酯、新戊二醇二(甲基)丙烯酸酯、甘油二(甲基)丙烯酸酯、甘油縮水甘油醚二(甲基)丙烯酸酯、1,6-己二醇二(甲基)丙烯酸酯、1,9-壬二醇二(甲基)丙烯酸酯、三環癸烷二甲醇二(甲基)丙烯酸酯、雙酚A聚乙氧基二(甲基)丙烯酸酯、雙酚A聚烷氧基二(甲基)丙烯酸酯、雙酚F聚烷氧基二(甲基)丙烯酸酯、聚伸烷基二醇二(甲基)丙烯酸酯、三羥甲基丙烷三氧基乙基(甲基)丙烯酸酯、ε-己內酯改性三(2-羥基乙基)異氰尿酸酯三(甲基)丙烯酸酯、季戊四醇三(甲基)丙烯酸酯、丙氧化季戊四醇三(甲基)丙烯酸酯、乙氧化季戊四醇三(甲基)丙烯酸酯、季戊四醇四(甲基)丙烯酸酯、丙氧化季戊四醇四(甲基)丙烯酸酯、乙氧化季戊四醇四(甲基)丙烯酸酯、二季戊四醇六(甲基)丙烯酸酯、聚乙二醇二(甲基)丙烯酸酯、三(丙烯醯氧基乙基)異氰尿酸酯、季戊四醇四(甲基)丙烯酸酯、二季戊四醇六(甲基)丙烯酸酯、二季戊四醇五(甲基)丙烯酸酯、三季戊四醇六(甲基)丙烯酸酯、三季戊四醇五(甲基)丙烯酸酯、羥基特戊酸新戊二醇二(甲基)丙烯酸酯、羥基特戊酸新戊二醇之ε-己內酯加成物之二(甲基)丙烯酸酯、三羥甲基丙烷三(甲基)丙烯酸酯、烷氧基化三羥甲基丙烷三(甲基)丙烯酸酯、二三羥甲基丙烷四(甲基)丙烯酸酯等紫外線硬化型多官能單體類，此外可列舉：聚酯(甲基)丙烯酸酯、環氧(甲基)丙烯酸酯、(甲基)丙烯酸胺基甲酸酯、聚醚(甲基)丙烯酸酯等多官能丙烯酸酯低聚物類，此外還可列舉多官能丙烯醯胺等。 於上述列舉中，就提高對被黏著體之密接性或濕熱白化抑制效果之觀點而言，於上述多官能(甲基)丙烯酸酯單體中，較佳為含有羥基或羧基、醯胺基等極性官能基之多官能單體或低聚物。其中，較佳為使用具有羥基或醯胺基之多官能(甲基)丙烯酸酯。 就防止濕熱白化之觀點而言，較佳為含有疏水性之丙烯酸酯單體與親水性之丙烯酸酯單體作為上述(甲基)丙烯酸酯共聚物(A1)、即接枝共聚物之幹成分，進而較佳為使用具有羥基之多官能(甲基)丙烯酸酯作為交聯劑(B)。 又，為了調整密接性或耐濕熱性、耐熱性等效果，亦可進而添加與交聯劑(B)反應之單官能或多官能之(甲基)丙烯酸酯。 關於交聯劑(B)之含量，就使作為黏著劑組合物之柔軟性與凝聚力平衡之觀點而言，相對於上述(甲基)丙烯酸系共聚物(A)100質量份，較佳為以0.1～20質量份之比率含有，其中尤佳為0.5質量份以上或15質量份以下之比率，其中尤佳為1質量份以上或13質量份以下之比率。 [光聚合起始劑(C)] 本黏著片所使用之光聚合起始劑(C)係作為交聯劑(B)之交聯反應中之反應引發助劑發揮功能者，較佳為藉由照射可見光線、例如380 nm～700 nm之波長區域之光線，產生自由基而成為基礎樹脂之聚合反應之起點者。但是，可藉由僅照射可見光線而產生自由基，又，亦可藉由照射可見光區域以外之波長區域之光線而產生自由基。 就該觀點而言，光聚合起始劑(C)之波長405 nm下之吸光係數尤佳為10 mL/(g∙cm)以上，其中尤佳為15 mL/(g∙cm)以上，其中尤佳為25 mL/(g∙cm)以上。另一方面，作為波長405 nm下之吸光係數之上限，較佳為1×104 mL/(g∙cm)以下，更佳為1×103 mL/(g∙cm)以下。 本發明中之吸光係數相當於將光聚合起始劑(C)設為濃度1 g/L之甲醇溶液時之光程長1 cm時之吸光度。再者，光聚合起始劑(C)之吸光係數並非意指僅吸收特定波長之光，而意指特定波長之光之分解性能(自由基產生能)。具體而言，「波長405 nm下之吸光係數」係指照射波長405 nm之光時之光聚合起始劑之分解性能(自由基產生能)。 作為波長405 nm下之吸光係數為10 mL/(g∙cm)以上之光聚合起始劑，例如可列舉：2-苄基-2-二甲基胺基-1-(4-嗎啉基苯基)丁烷-1-酮、2-(4-甲基苄基)-2-二甲基胺基-1-(4-嗎啉基苯基)丁烷-1-酮、雙(η5 -2,4-環戊二烯-1-基)-雙(2,6-二氟-3-(1H-吡咯-1-基)苯基)鈦、雙(2,4,6-三甲基苯甲醯基)-苯基氧化膦、2,4,6-三甲基苯甲醯基二苯基氧化膦、(2,4,6-三甲基苯甲醯基)乙氧基苯基氧化膦、雙(2,6-二甲氧基苯甲醯基)2,4,4-三甲基戊基氧化膦、9-氧硫𠮿、2-氯-9-氧硫𠮿、3-甲基-9-氧硫𠮿、2,4-二甲基-9-氧硫𠮿、蒽醌、2-甲基蒽醌、2-乙基蒽醌、2-第三丁基蒽醌、2-胺基蒽醌、1,2-辛二酮-1-(4-(苯硫基)-2-(o-苯甲醯基肟))、1-[9-乙基-6-(2-甲基苯甲醯基)-9H-咔唑-3-基]-乙酮-1-(o-乙醯基肟)、樟腦醌，此外還可列舉三𠯤系光聚合起始劑等。此外，亦包含光聚合起始劑(C)與(甲基)丙烯酸系共聚物(A)化學鍵結之態樣。 該等可使用該等中之任一種或其衍生物，又，亦可組合該等中之兩種以上而使用。又，亦可與波長405 nm下之吸光係數未達10 mL/(g∙cm)之光聚合起始劑併用。 光聚合起始劑根據自由基產生機制大致分類為兩種，大致分為裂解型光聚合起始劑與吸氫型光聚合起始劑，該裂解型光聚合起始劑係可使光聚合性起始劑自身之單鍵裂解分解而產生自由基，該吸氫型光聚合起始劑係光激發之起始劑與系中之氫供與體形成激發錯合物而可使氫供與體之氫轉移。 該等中之裂解型光聚合起始劑於藉由光照射產生自由基時分解而成為其他化合物，一旦被激發便不再具有作為反應起始劑之功能。因此，若使用該分子內裂解型作為於可見光線區域具有吸收波長之光聚合起始劑(C)，則與使用吸氫型之情形相比，於藉由光線照射使黏著片交聯後，光線反應性之光聚合性起始劑不易殘留於本黏著劑組合物中，導致黏著片之非預期之經時變化或交聯促進、分解促進之可能性較低，因此較佳。又，關於光聚合性起始劑特有之著色，先前於添加對黏著劑照射可見光線而使其硬化之光聚合起始劑之情形時，有著色之虞，但反應分解物之可見光線區域之吸收消失，較佳為適當選擇消色者。 另一方面，吸氫型光聚合起始劑於藉由紫外線等活性能量線照射進行自由基產生反應時，不會產生如裂解型光聚合起始劑之分解物，因此反應結束後不易成為揮發成分，可減少對被黏著體之損傷。 作為上述裂解型光聚合起始劑，例如可列舉：2,2-二甲氧基-1,2-二苯基乙烷-1-酮、1-羥基環己基苯基酮、2-羥基-2-甲基-1-苯基-丙烷-1-酮、1-(4-(2-羥基乙氧基)苯基)-2-羥基-2-甲基-1-丙烷-1-酮、2-羥基-1-[4-{4-(2-羥基-2-甲基-丙醯基)苄基}苯基]-2-甲基-丙烷-1-酮、低聚(2-羥基-2-甲基-1-(4-(1-甲基乙烯基)苯基)丙酮)、苯基乙醛酸甲酯、2-苄基-2-二甲基胺基-1-(4-嗎啉基苯基)丁烷-1-酮、2-甲基-1-[4-(甲硫基)苯基]-2-嗎啉基丙烷-1-酮、2-(二甲基胺基)-2-[(4-甲基苯基)甲基]-1-[4-(4-嗎啉基)苯基]-1-丁酮、雙(2,4,6-三甲基苯甲醯基)-苯基氧化膦、2,4,6-三甲基苯甲醯基二苯基氧化膦、(2,4,6-三甲基苯甲醯基)乙氧基苯基氧化膦、雙(2,6-二甲氧基苯甲醯基)2,4,4-三甲基戊基氧化膦、或其等之衍生物等。 其中，就利用裂解型光聚合性起始劑，反應後成為分解物且消色之方面而言，較佳為雙(2,4,6-三甲基苯甲醯基)-苯基氧化膦、2,4,6-三甲基苯甲醯基二苯基氧化膦、(2,4,6-三甲基苯甲醯基)乙氧基苯基氧化膦、雙(2,6-二甲氧基苯甲醯基)-2,4,4-三甲基戊基氧化膦等醯基氧化膦系光起始劑。 進而，就與包含具備巨分子單體作為枝成分之接枝共聚物之丙烯酸系共聚物之配合性而言，較佳為使用2,4,6-三甲基苯甲醯基二苯基氧化膦、(2,4,6-三甲基苯甲醯基)乙氧基苯基氧化膦、雙(2,6-二甲氧基苯甲醯基)-2,4,4-三甲基戊基氧化膦等作為光聚合起始劑(C)。 光聚合起始劑(C)之含量並無特別限制。例如相對於(甲基)丙烯酸系共聚物(A)100質量份，尤佳為以0.1～10質量份之比率含有，其中尤佳為以0.2質量份以上或5質量份以下之比率含有，其中尤佳為以0.5質量份以上或3質量份以下之比率含有。但是，就與其他要素之平衡而言，亦可超過該範圍。光聚合起始劑可使用1種或組合2種以上而使用。 [紫外線吸收劑(D)] 紫外線吸收劑(D)只要為可吸收紫外線之物質即可，作為標準，較佳為藉由紫外線吸收劑(D)之添加，可使透明雙面黏著片之波長380 nm下之吸光度為0.3 mL/(g∙cm)以上、尤其為0.5 mL/(g∙cm)以上、尤其為1.0 mL/(g∙cm)以上之物質。 再者，波長380 nm下之吸光度係根據以下之式求出。 A380 ＝-Log(T380 /100) A380 ：波長380 nm下之吸光度 T380 ；透明雙面黏著片之380 nm下之透過率(%) 作為紫外線吸收劑(D)，例如較佳為具有選自由苯并***結構、二苯甲酮結構、三𠯤結構、苯甲酸酯結構、草醯苯胺結構、水楊酸酯結構及氰基丙烯酸酯結構所組成之群中之1種或2種以上之結構者。 其中，就紫外線吸收性之觀點而言，較佳為具有選自由苯并***結構、三𠯤結構及二苯甲酮結構所組成之群中之1種或2種以上之結構者。 又，就與包含具備巨分子單體作為枝成分之接枝共聚物之丙烯酸系共聚物之配合性之觀點而言，較佳為使用苯并***結構或二苯甲酮結構等作為紫外線吸收劑(D)。 紫外線吸收劑(D)之含量並無特別限制。例如相對於(甲基)丙烯酸系共聚物(A)100質量份，尤佳為以0.01～10質量份之比率含有，其中尤佳為以0.1質量份以上或5質量份以下之比率含有，其中尤佳為以0.2質量份以上或3質量份以下之比率含有。但是，就與其他要素之平衡而言，亦可超過該範圍。 就吸收紫外線且於除該紫外線以外之可見光區域開始光聚合之觀點而言，相對於光聚合起始劑(C)100質量份之紫外線吸收劑(D)之比率較佳為25～400質量份，其中尤佳為50質量份以上或300質量份以下，其中尤佳為80質量份以上或250質量份以下。紫外線吸收劑亦可使用1種或組合2種以上而使用。 [其他成分] 本黏著片亦可含有調配於通常之黏著組合物之公知成分作為上述以外之成分。例如可適當含有黏著賦予樹脂、或抗氧化劑、光穩定化劑、金屬減活劑、防銹劑、防老化劑、吸濕劑、防水解劑、增感劑、抗靜電劑、消泡劑、無機粒子等各種添加劑。 又，視需要，亦可視需要適當含有反應觸媒(三級胺系化合物、四級銨系化合物、月桂酸錫化合物等)。 [較佳之組成例] 作為本黏著劑組合物之尤佳組成之一例，可列舉如下組成例，即，含有包含具備巨分子單體作為枝成分之接枝共聚物之丙烯酸系共聚物作為(甲基)丙烯酸系共聚物(A)，含有二官能、三官能等多官能(甲基)丙烯酸酯化合物作為交聯劑(B)，含有裂解型光聚合起始劑作為光聚合起始劑(C)，且含有具有苯并***結構或二苯甲酮結構之紫外線吸收劑作為紫外線吸收劑(D)。但是，並不限定於此種組成。 [積層構成] 本黏著片可為包含單一層之片材，亦可為積層2層以上而成之多層片材。 於將本黏著片製成多層黏著片之情形時，即形成具備中間層與最外層之積層構成之黏著片之情形時，較佳為由本黏著劑組合物形成該最外層。 於將本黏著片設為多層構成之情形時，各最外層之厚度與中間層之厚度之比率較佳為1：1～1：20，其中進而較佳為1：2～1：10。 若中間層之厚度為上述範圍，則積層體中之黏著材層之厚度之影響不會過大，不會因過於柔軟而裁剪或操作之作業性變差，因而較佳。 又，若最外層為上述範圍，則不存在對凹凸或彎曲之面之追隨性較差之情況，可維持對被黏著體之接著力或潤濕性，因而較佳。 作為將本黏著片設為多層構成之情形之一例，可列舉具備中間層(α層)與表層(β層)之多層構成，該中間層(α層)包含本黏著劑組合物、即含有(甲基)丙烯酸系共聚物(A)、交聯劑(B)、波長405 nm下之吸光係數為10 mL/(g∙cm)以上之光聚合起始劑(C)及紫外線吸收劑(D)之黏著劑樹脂組合物，該表層(β層)含有(甲基)丙烯酸系共聚物(A)及交聯劑(B)，且不含紫外線吸收劑(D)。 作為具體之積層構成，可列舉β層/α層/β層、β層/α層/β層/α層/β層等。其中，更佳為β層/α層/β層即2種3層。亦可視需要於α層與β層之間介隔以釋氣阻隔層為代表之其他層。 藉由設置含有(甲基)丙烯酸系共聚物(A)及交聯劑(B)且不含紫外線吸收劑(D)之表層(β層)，可抑制α層內之紫外線吸收劑(D)滲出。 再者，於形成β層之樹脂組合物中含有光聚合起始劑(C)、或其分解生成物、或者紫外線吸收劑(D)之情形時，例如將α層(中間層)與β層(表層)重疊後進行光照射時，有於作為表層之β層吸收光而將到達作為中間層之α層之光截斷、或紫外線吸收劑(D)自β層轉移至α層而阻礙α層之光硬化之虞。 就上述觀點而言，β層較佳為不具有光硬化性，更佳為具有熱硬化性。其中，β層更佳為不含光聚合起始劑(C)及紫外線吸收劑(D)之樹脂組合物。 於具備上述α層及β層之多層構成中，關於α層所使用之交聯劑(B)，就提高與β層之密接性或濕熱白化抑制效果之觀點而言，較佳為含有羥基或羧基等極性官能基之多官能單體或低聚物。其中，更佳為使用具有羥基之多官能(甲基)丙烯酸系單體。 α層之交聯劑(B)之含量較佳為相對於α層之丙烯酸系共聚物(A)100質量份為0.5～50質量份之比率，其中較佳為1質量份以上或40質量份以下之比率，其中較佳為5質量份以上或30質量份以下之比率。藉由以該範圍含有交聯劑(B)，硬化反應於短時間內充分進行，因此容易使硬化後之可靠性與耐濕熱白化性、柔軟性、成形為片狀時之加工適性等平衡化。 另一方面，β層所使用之交聯劑(B)就熱硬化性之觀點而言，較佳為含有選自(甲基)丙烯醯基、環氧基、異氰酸酯基、三聚氰胺基、二醇基、矽氧烷基及胺基中之至少1個有機官能基之交聯劑。 β層之交聯劑(B)之含量較佳為相對於β層之丙烯酸系共聚物(A)100質量份為0.1～20質量份之比率，其中較佳為0.2質量份以上或10質量份以下之比率。藉由以該範圍含有交聯劑(B)，硬化反應於短時間內充分進行，因此於硬化後，作為黏著片，容易使黏性與可靠性、耐發泡性、階差吸收性(異物嚙入性)、柔軟性、成形為片狀時之加工適性等平衡化。 又，更佳為相較於β層而於α層中添加更多之交聯劑(B)。對硬化後之α層賦予較高之彈性而使其發揮作為芯材之功能，可對黏著片賦予優異之操作性。 於具備上述α層及β層之多層構成中，關於α層，就吸收紫外線且於除該紫外線以外之可見光區域開始光聚合之觀點而言，於α層中，相對於光聚合起始劑(C)100質量份，紫外線吸收劑(D)較佳為含有25～400質量份，其中更佳為50質量份以上或300質量份以下，進而較佳為80質量份以上或250質量份以下。 於具備上述α層及β層之多層構成中，關於積層α層與β層之順序、硬化之順序並無特別限定。具體而言，可例示以下之積層方法。 方法I：將未硬化之α層與β層積層後，藉由光照射或熱等使α層與β層硬化之方法。 方法II：於未硬化之α層積層藉由熱等而硬化之β層後，藉由光照射使α層硬化之方法。 方法III：於藉由光照射而硬化之α層積層未硬化之β層後，藉由熱等使β層硬化之方法。 方法IV：將分別成形且硬化之α層及β層重疊之方法。 其中，就層間密接力較強，耐濕熱發泡性、可靠性優異，且可抑制紫外線吸收劑之滲出而言，更佳為方法II。 β層較佳為進行熱硬化。 關於用以使β層硬化之加熱溫度，並無特別限定，可根據β層中所含之交聯劑(B)之種類與量而適當調整。若考慮硬化前之樹脂組合物之操作性或樹脂之耐熱性等，則具體而言，較佳為40～200℃，其中更佳為50℃以上或180℃以下，其中進而較佳為60℃以上或150℃以下。 另一方面，α層較佳為進行光硬化。 用以使α層硬化之光照射量以波長405 nm為基準較佳為100～8000 mJ/cm2 ，其中更佳為500 mJ/cm2 以上或5000 mJ/cm2 以下，其中進而較佳為1000 mJ/cm2 以上或4000 mJ/cm2 以下。 作為出射光之光源，例如可列舉高壓水銀燈、金屬鹵化物燈、LED燈等。 此時，亦可將實質上不含波長380 nm以下之波長之光之光線、較佳為可見光線照射至本黏著片，使本黏著片進行光交聯。所謂「實質上不含未達380 nm之波長之光之光線」係指未達380 nm之波長之光之透光率未達10%之光。作為照射不含紫外線區域之波長之光之可見光線之方法，可使用僅出射不含紫外線區域之波長之光之可見光線之光源，亦可隔著不使紫外線區域之波長之光透過之濾光片照射。 於具備上述α層及β層之多層構成中，α層之厚度較佳為10～400 μm，其中更佳為20 μm以上或300 μm以下，其中進而較佳為30 μm以上或200 μm以下。 β層之厚度較佳為1～60 μm，其中更佳為3 μm以上或40 μm以下，其中進而較佳為5 μm以上或25 μm以下。 α層之厚度與β層之厚度之比率較佳為1：1～1：20，其中更佳為1：2～1：15。 若α層(中間層)之厚度為上述範圍，則容易獲得紫外線吸收性能，且可容易兼顧到α層之光硬化性能。又，不存在過於柔軟而裁剪或操作之作業性變差之情況，因而較佳。若β層(表層)之厚度為上述範圍，則不存在對凹凸或彎曲之面之追隨性較差之情況，可維持對被黏著體之接著力或潤濕性，因而較佳。 [片材厚度] 關於本黏著片之厚度，藉由使片材厚度變薄，可響應薄壁化要求，另一方面，若使片材厚度過薄，則有例如於被黏著面具有凹凸部之情形時無法充分地追隨於凹凸、或無法發揮充分之接著力之可能性。 就該觀點而言，本黏著片之厚度較佳為20～500 μm，其中尤佳為25 μm以上或350 μm以下，其中尤佳為50 μm以上或250 μm以下。 [特性] 本黏著片之紫外線透過率(JIS K7361-1)較佳為於波長380 nm下為50%以下，其中進而較佳為30%以下，其中進而較佳為10%以下。 另一方面，作為可見光區域之波長420 nm下之透光率較佳為70%以上，更佳為80%以上，進而較佳為85%以上。 本發明之透明雙面黏著片之100℃下之黏度較佳為50 Pa∙s～5000 Pa∙s，其中更佳為100 Pa∙s以上或3000 Pa∙s以下，其中更佳為150 Pa∙s以上或2500 Pa∙s以下。 ＜黏著片積層體＞ 本黏著片可直接單獨使用。又，亦可與其他構件積層而使用。 (本黏著片積層體) 例如，可於本黏著片之一側或兩側，積層膜、例如脫模膜或保護膜或積層該等而成之膜而構成黏著片積層體(稱為「本黏著片積層體」)。 可例示如下情形：於本黏著片積層體中，一側或兩側之脫模膜為波長410 nm以下之光之透光率為40%以下之脫模膜。其原因在於，若至少一脫模膜之波長410 nm以下之光之透光率為40%以下，則藉由將該脫模膜積層於本黏著片，即便本黏著片含有波長405 nm下之吸光係數為10 mL/(g∙cm)以上之光聚合起始劑(C)，亦可有效地防止因可見光之照射而推進光聚合之情況。 就該觀點而言，較佳為一個或兩個脫模膜之波長410 nm以下之光之透光率為40%以下，其中進而較佳為30%以下，其中進而較佳為20%以下。 此處，作為波長410 nm以下之光之透光率為40%以下之脫模膜、即具有將可見光及紫外光之透光之一部分遮斷之作用之脫模膜，例如可列舉於包含調配有紫外線吸收劑之聚酯系、聚丙烯系、聚乙烯系樹脂之鑄膜或延伸膜塗佈聚矽氧樹脂而進行脫模處理者。又，可列舉於在包含調配有紫外線吸收劑之聚酯系、聚丙烯系、聚乙烯系樹脂之層之單面或雙面成形包含不含紫外線吸收劑之樹脂之層而成的多層鑄膜或延伸膜之一面，塗佈聚矽氧樹脂而進行脫模處理者。又，可列舉於包含聚酯系、聚丙烯系、聚乙烯系樹脂之鑄膜或延伸膜之一面塗佈含有紫外線吸收劑之塗料而設置紫外線吸收層，進而於該紫外線吸收層上塗佈聚矽氧樹脂而進行脫模處理者。又，可列舉於包含聚酯系、聚丙烯系、聚乙烯系樹脂之鑄膜或延伸膜之一面塗佈含有紫外線吸收劑之塗料而設置紫外線吸收層，於另一面塗佈聚矽氧樹脂而進行脫模處理者。又，可列舉將一面經脫模處理之包含聚酯系、聚丙烯系、聚乙烯系樹脂之樹脂膜之另一面與另外準備之未實施脫模處理之樹脂膜經由含有紫外線吸收劑之接著層或黏著層進行積層而成者。 上述脫模膜亦可視需要具有抗靜電層或硬塗層、增黏層等其他層。 脫模膜之厚度若過厚則裁剪加工性較差，若過薄則操作性較差，有容易於黏著片產生凹痕之可能性。就該觀點而言，脫模膜之厚度較佳為20 μm以上且300 μm以下，其中較佳為25 μm以上或250 μm以下，其中較佳為38 μm以上或200 μm以下。 於設為在兩側積層有脫模膜之構成之情形時，較佳為使一脫模膜與另一脫模膜之厚度或剝離力不同。 又，可例示如下情形：於本黏著片積層體中，一側或兩側之膜為波長380 nm以上且410 nm以下之光之透光率為40%以下之膜、例如脫模膜或保護膜或積層該等而成之膜。即，於包含含有(甲基)丙烯酸系共聚物(A)、交聯劑(B)、波長405 nm下之吸光係數為10 mL/(g∙cm)以上之光聚合起始劑(C)及紫外線吸收劑(D)之黏著劑樹脂組合物的透明雙面黏著片之一側或兩側，積層波長380 nm以上且410 nm以下之光之透光率為40%以下之膜，藉此可抑制至少波長405 nm暴露於該透明雙面黏著片，因此可抑制光聚合起始劑(C)產生自由基。 就該觀點而言，本黏著片積層體中之一側或兩側之膜進而較佳為波長380 nm以上且410 nm以下之光之透光率為40%以下，其中進而較佳為30%以下，其中進而較佳為20%以下，其中進而較佳為10%以下。 再者，作為較佳之構成例，可列舉於本黏著片積層體之單面或雙面積層波長410 nm以下之光之透光率為40%以下之表面保護膜的構成。 其原因在於，於本黏著片積層體之至少一面積層波長410 nm以下之光之透光率為40%以下之表面保護膜，藉此，即便本黏著片含有波長405 nm下之吸光係數為10 mL/(g∙cm)以上之光聚合起始劑(C)，亦可有效地防止因可見光之照射而推進光聚合。 就該觀點而言，積層於本黏著片積層體之一面或兩面之表面保護膜較佳為波長410 nm以下之光之透光率為40%以下，其中進而較佳為30%以下，其中進而較佳為20%以下。 此處，作為波長410 nm以下之光之透光率為40%以下之表面保護膜、即具有將可見光及紫外光之透光之一部分遮斷之作用之表面保護膜，例如可列舉於聚酯系、聚丙烯系、聚乙烯系鑄膜或延伸膜之一面，塗佈具有再剝離性之微黏著樹脂，於另一面具備塗佈含有紫外線吸收劑之塗料而成之紫外線吸收層的積層膜。又，可列舉於聚丙烯系、聚乙烯系鑄膜或延伸膜之一面，塗佈調配有紫外線吸收劑之具有再剝離性之微黏著樹脂者。又，可列舉於包含調配有紫外線吸收劑之聚酯系、聚丙烯系、聚乙烯系樹脂之鑄膜或延伸膜，塗佈具有再剝離性之微黏著樹脂者。又，可列舉於在包含調配有紫外線吸收劑之聚酯系、聚丙烯系、聚乙烯系樹脂之層之單面或雙面成形包含不含紫外線吸收劑之樹脂之層而成之多層鑄膜或延伸膜之一面，塗佈具有再剝離性之微黏著樹脂者。又，可列舉於包含聚酯系、聚丙烯系、聚乙烯系樹脂之鑄膜或延伸膜之一面塗佈含有紫外線吸收劑之塗料而設置紫外線吸收層，進而於該紫外線吸收層上塗佈具有再剝離性之微黏著樹脂者。又，可列舉於包含聚酯系、聚丙烯系、聚乙烯系樹脂之鑄膜或延伸膜之一面塗佈含有紫外線吸收劑之塗料而設置紫外線吸收層，於另一面塗佈具有再剝離性之微黏著樹脂者。又，可列舉將於一面塗佈有具有再剝離性之微黏著樹脂之包含聚酯系、聚丙烯系、聚乙烯系樹脂之樹脂膜之另一面與另外準備之樹脂膜經由含有紫外線吸收劑之接著層或黏著層進行積層而成者等。 上述表面保護膜亦可視需要具有抗靜電層或硬塗層、增黏層等其他層。 (本圖像顯示裝置構成用積層體) 又，亦可經由本黏著片將2個圖像顯示裝置用構成構件進行積層而構成圖像顯示裝置構成用積層體(稱為「本圖像顯示裝置構成用積層體」)。 此時，作為2個圖像顯示裝置用構成構件，例如可列舉由觸控感測器、圖像顯示面板、表面保護面板及偏光膜所組成之群中之任一個、或兩種以上之組合。 作為本圖像顯示裝置構成用積層體之具體例，例如可列舉如下構成：脫模片材/本黏著片/觸控面板、脫模片材/本黏著片/保護面板、脫模片材/本黏著片/圖像顯示面板、圖像顯示面板/本黏著片/觸控面板、圖像顯示面板/本黏著片/保護面板、圖像顯示面板/本黏著片/觸控面板/本黏著片/保護面板、偏光膜/本黏著片/觸控面板、偏光膜/本黏著片/觸控面板/本黏著片/保護面板等。但是，並不限定於該等積層例。 上述觸控面板亦包含使保護面板內置觸控面板功能之結構體、或使圖像顯示面板內置觸控面板功能之結構體。 於本圖像顯示裝置構成用積層體中，上述2個圖像顯示裝置構成構件中之至少一個亦可為具備紫外線吸收性能者、例如含有紫外線吸收劑者。 由於本黏著片並非藉由紫外線而硬化者，而是藉由可見光而硬化，故而即便圖像顯示裝置構成構件為具備紫外線吸收性能者，亦可藉由透過該圖像顯示裝置構成構件照射可見光而使本黏著片硬化。 (本圖像顯示裝置) 可使用如上所述之本黏著片或本圖像顯示裝置構成用積層體構成圖像顯示裝置(稱為「本圖像顯示裝置」)。 作為本圖像顯示裝置，例如可構成液晶顯示器、有機EL顯示器、無機EL顯示器、電子紙、電漿顯示器及微機電系統(MEMS)顯示器等圖像顯示裝置。 於本圖像顯示裝置中，構成圖像顯示裝置之圖像顯示裝置構成構件中之至少一個亦可為具備紫外線吸收性能者、例如含有紫外線吸收劑者。 由於本黏著片並非藉由紫外線而硬化者，而是藉由可見光而硬化，故而即便圖像顯示裝置構成構件為具備紫外線吸收性能者，亦可藉由透過該圖像顯示裝置構成構件照射可見光而使本黏著片硬化。 ＜本黏著片之特徵與使用方法＞ 本黏著片具備紫外線吸收功能、及藉由紫外線區域以外之波長之光線、尤其可見光線之照射而硬化之硬化性。利用此種本黏著片之特性，例如可以如下方式製作圖像顯示裝置構成用積層體。 於將本黏著劑組合物形成為片狀後(片材製作步驟)，經由光硬化前之本黏著片將2個圖像顯示裝置構成構件進行積層(一次貼附步驟)，其次，照射至少波長405 nm之光、例如包含可見光區域之波長之光線之光，使上述本黏著片進行光交聯而硬化(二次貼附步驟)，藉此，可製作圖像顯示裝置構成用積層體。 包含可見光區域之波長之光線之光亦可包含紫外線區域、即波長380 nm以下之波長之光，但於積層之圖像顯示裝置構成構件為容易紫外線劣化之構件之情形時，較佳為照射實質上不含波長380 nm以下之波長之光之光線、即可見光線，使本黏著片進行光交聯而硬化(二次貼附步驟)。 (片材製作步驟) 可將本黏著劑組合物成形為片狀而製作本黏著片。 作為將本黏著劑樹脂組合物成形為片狀之方法，可任意採用目前公知之方法。 此時，如上所述，亦可將本黏著劑樹脂組合物於上述脫模膜上成膜為片狀而製作本黏著片。 又，亦可將本黏著劑樹脂組合物於圖像顯示裝置構成構件上呈片狀製成膜，並於該圖像顯示裝置構成構件上積層本黏著片。 (一次貼附步驟) 只要本黏著片具備自黏性(黏性)，則經由本黏著片重疊2個圖像顯示裝置構成構件便可一次貼附。 例如，只要本黏著片為將包含具備巨分子單體作為枝成分之接枝共聚物之丙烯酸系共聚物(A1)作為基礎聚合物者，則可於室溫狀態下保持片狀並且顯示自黏性，而且於未交聯狀態下，於常態、即於室溫附近，可具有適度之接著性、例如可剝離之程度之接著性(稱為“黏性”)，因此可易於進行貼附時之定位等。進而又，若於未交聯狀態下加熱，則可熔融或流動(熱熔性)，因此可追隨於印刷階差等凹凸部而填充黏著劑，可不產生氣泡等地填充。 積層時使用之貼合裝置可使用公知裝置。例如，可列舉：具備加熱板之電熱加壓機、或膜片方式之貼合機、輥貼合機、真空貼合機、手壓輥等。 再者，於本黏著片使用包含具備巨分子單體作為枝成分之接枝共聚物之丙烯酸系共聚物(A1)作為基礎聚合物之情形時，可於通常狀態、即室溫狀態下賦予優異之保管穩定性或裁剪加工性。並且，由於具有自黏性(黏性)，故而僅將本黏著片壓抵於被黏著體便可簡單地獲得貼附程度之黏著性，因此容易進行貼附黏著材之定位，作業上非常便利。 進而，由於形狀保持性優異，故而可預先加工成任意形狀，因此亦可對照所要積層之圖像顯示裝置構成構件之尺寸，預先將成形於脫模膜上之本黏著片進行切割。 此時之切割方法一般為利用湯姆森(Thomson)刀之沖裁、利用超級切割機或雷射之切割，更佳為以容易剝離脫模膜之方式將正背任一者之脫模膜以邊框狀殘留而進行半切割。 於本黏著片具備熱熔性、即具備藉由加熱而柔軟化或流體化之性質之情形時，較佳為加熱本黏著片而積層2個圖像顯示裝置構成構件。藉由加熱本黏著片使其柔軟化或流體化，即便於被黏著面具有凹凸，亦可藉由加熱黏著片，追隨於凹凸而於該凹凸亦無間隙地進行填充。 作為本黏著片之加熱機構，例如可使用各種恆溫槽、或加熱板、電磁加熱裝置、加熱輥等。為了更有效率地進行貼合與加熱，例如較佳為使用電熱加壓機、或膜片方式之貼合機、輥貼合機等。 此時，亦可藉由加熱圖像顯示裝置構成構件中之一者或兩者，而加熱本黏著片。 此時，若本黏著片之軟化溫度為50℃以上，則可使加工特性或常溫下之保管特性充分。另一方面，若本黏著片之軟化溫度為100℃以下，則不僅可抑制對圖像顯示面板或前表面面板之熱損傷，而且亦可防止本黏著片過度流動而溢出。 由此，本黏著片之軟化溫度較佳為50～100℃，其中進而較佳為55℃以上或95℃以下，其中進而較佳為60℃以上或90℃以下。 加熱本黏著片時，較佳為經由本黏著片將2個圖像顯示裝置構成構件重疊而積層後，將積層體於減壓環境下進行加熱。 藉由於減壓環境下加熱積層體，可防止貼合後於本黏著片內混入氣泡或混入異物。 (二次貼附步驟) 於二次貼附步驟中，對於經由本黏著片積層2個圖像顯示裝置構成構件而成之積層體，自至少一圖像顯示裝置構成用構件之外側，透過該圖像顯示裝置構成用構件，將至少波長405 nm之光、例如包含可見光區域之波長之光線之光、即可見光線照射至本黏著片，使本黏著片進行光交聯而硬化。 藉由如此光交聯，可使本黏著片充分交聯，因此可使其具有儘可能地充分對抗例如自保護面板等圖像顯示裝置構成構件產生之釋氣之氣壓的黏著力與凝聚力。並且，由於本黏著片具有紫外線吸收性，故而可抑制黏著片自身以及圖像顯示裝置構成構件之因紫外線所致之劣化。 至少波長405 nm之光可自包含例如選自太陽、螢光燈、LED、有機EL、無機EL及圖像顯示裝置用發光模組中之至少1種或2種以上之組合之光源進行照射。 照射可見光線時，較佳為照射實質上不含紫外線區域之波長之光、例如未達365 nm之波長之光之可見光線。 此處，所謂「實質上不含未達365 nm之波長之光」係指未達365 nm之波長之光之發光強度未達1 mW/cm2 。 其中，較佳為將至少波長405 nm之光、例如包含可見光區域之波長之光線且實質上不含波長380 nm以下之波長之光的光線照射至本黏著片，使本黏著片進行光交聯而硬化。 此處，所謂「實質上不含380 nm以下之波長之光」，意指380 nm以下之波長之光之發光強度為5 mW/cm2 以下、較佳為1 mW/cm2 以下。 作為照射不含380 nm以下之波長之光、即紫外線區域之波長之光之可見光線之方法，亦可使用僅出射不含紫外線區域之波長之光之可見光線之光源。例如可使用包含選自太陽、螢光燈、LED、有機EL、無機EL及圖像顯示裝置用發光模組中之至少1種或2種以上之組合之光源。 又，亦可隔著不使紫外線區域之波長之光透過之濾光片而照射。例如，可列舉如下方法：使用亦出射紫外線區域之波長之光之高壓水銀燈或金屬鹵化物燈、氙弧燈、碳弧燈等發光燈或太陽光作為光源，隔著波長380 nm下之透光率未達10%且波長405 nm下之透光率為60%以上之濾光片，將可見光線照射至接著劑組合物。 上述濾光片亦可為構成本黏著片積層體之脫模膜、或積層於本黏著片積層體之表面而使用之表面保護膜。 調整可見光交聯之程度時，除了控制可見光之照射量之方法以外，亦可藉由隔著上述濾光片照射可見光，而以將可見光之透光之一部分遮斷之方式調整可見光交聯之程度。 ＜語句說明等＞ 再者，一般而言，所謂「片材」，於JIS之定義上係指較薄、其厚度相比於長度及寬度較小且平坦之製品，一般而言，所謂「膜」係指厚度相比於長度及寬度極小、最大厚度被任意地限定之較薄且平坦之製品，通常以輥之形式供給(日本工業標準JIS K6900)。然而，片材與膜之邊界並未限定，於本發明中，文語上無需區分兩者，因此，於本發明中，於稱為「膜」之情形時，亦包含「片材」，於稱為「片材」之情形時，亦包含「膜」。 又，於如圖像顯示面板、保護面板等般表達為「面板」之情形時，包含板體、片材及膜。 於本說明書中，於記載為「X～Y」(X、Y為任意數字)之情形時，若無特別說明，則包含「X以上且Y以下」之含義，並且亦包含「較佳為大於X」或「較佳為小於Y」之含義。 又，於記載為「X以上」(X為任意數字)之情形時，若無特別說明，則包含「較佳為大於X」之含義，於記載為「Y以下」(Y為任意數字)之情形時，若無特別說明，則亦包含「較佳為小於Y」之含義。 [實施例] 以下，藉由實施例及比較例進一步進行說明。但是，本發明並不限定於該等。 本實施例中測定之波長405 nm及波長365 nm下之光之累計光量係使用累計光量計(UIT-250，牛尾電機公司製造)進行測定。 [實施例1-1] 對作為(甲基)丙烯酸系共聚物(A)之包含數量平均分子量3000之聚甲基丙烯酸甲酯巨分子單體(Tg80℃)15質量份、丙烯酸丁酯81質量份、及丙烯酸4質量份之共聚物(A-1，質量平均分子量30萬)1 kg，添加作為交聯劑(B)之二甲基丙烯酸甘油酯(日油公司製造，Blemmer GMR)(B-1)100 g、作為光聚合起始劑(C)之Esacure KTO46(C-1)(Lanberti公司製造)15g、作為紫外線吸收劑(D)之2,6-二苯基-4-(2-羥基-4-己氧基苯基)-1,3,5-三𠯤(BASF公司製造，TINUVIN 1577)(D-1)5 g，並均勻混合，而獲得黏著劑組合物1。 光聚合起始劑(C-1)之405 nm下之吸光係數為7.4×101 (mL/(g∙cm))。 其次，將上述黏著劑組合物1於經剝離處理之聚對苯二甲酸乙二酯膜(三菱樹脂公司製造，DIAFOIL MRV，厚度100 μm)上以厚度成為100 μm之方式成形為片狀後，被覆經剝離處理之聚對苯二甲酸乙二酯膜(三菱樹脂公司製造，DIAFOIL MRQ，厚度75 μm)，製成黏著片積層體1。 [實施例1-2] 將作為(甲基)丙烯酸系共聚物(A)之數量平均分子量1400之聚甲基丙烯酸甲酯巨分子單體(Tg55℃)10質量份及(甲基)丙烯酸2-乙基己酯(Tg：-70℃)90質量份進行無規共聚而成的丙烯酸系接枝共聚物(A-2)(重量平均分子量：23萬)1 kg、作為交聯劑(B)之三環癸烷二甲基丙烯酸酯(新中村化學公司製造，製品名：DCP)(B-2)50 g、作為光聚合起始劑(C)之Irgacure 369(C-2)(BASF公司製造)15 g、以及作為紫外線吸收劑(D)之2-(2H-苯并***-2-基)-4,6-二第三戊基苯酚(城北化學公司製造，JF-80)(D-2)20 g進行均勻混合，製作黏著樹脂組合物2。 其次，於經剝離處理之聚對苯二甲酸乙二酯膜(三菱樹脂公司製造，DIAFOIL MRV，厚度100 μm)上，以成為100 μm之方式塗佈黏著劑組合物4後，被覆經剝離處理之聚對苯二甲酸乙二酯膜(三菱樹脂公司製造，DIAFOIL MRQ，厚度75 μm)，製成黏著片積層體2。 光聚合起始劑(C-2)之405 nm下之吸光係數為1.6×102 (mL/(g∙cm))。 [實施例1-3] 對作為(甲基)丙烯酸系共聚物(A)之包含(甲基)丙烯酸2-乙基己酯76質量份、乙酸乙烯酯20質量份及丙烯酸4質量份之共聚物(A-3，質量平均分子量40萬)1 kg，添加作為交聯劑(B)之丙氧化季戊四醇四丙烯酸酯(新中村化學公司製造，ATM-4P)(B-3)200 g、作為光聚合起始劑(C)之Irgacure 819(C-3)(BASF公司製造)7 g、以及作為紫外線吸收劑(D)之2,2'-二羥基-4-甲氧基二苯甲酮(Chemipro Kasei公司製造，Kemisorb111)(D-3)10 g，並均勻混合，獲得黏著劑組合物3。 光聚合起始劑(C-3)之405 nm下之吸光係數為9.0×102 (mL/(g∙cm))。 以經剝離處理之2片聚對苯二甲酸乙二酯膜(三菱樹脂公司製造，DIAFOIL MRF，厚度75 μm/三菱樹脂公司製造，DIAFOIL MRT，厚度38 μm)夾著黏著樹脂組合物3，並以厚度成為100 μm之方式賦形為片狀，製成中間層用片材(α)。 對市售之包含丙烯酸系共聚物(A-4，質量平均分子量130萬)之黏著劑溶液(綜研化學公司製造，SK-Dyne1882，固形物成分濃度約17%)1 kg，添加作為異氰酸酯系交聯劑之L-45(B-5)(綜研化學公司製造)1.85 g及作為環氧系交聯劑之E-5XM(B-6)(綜研化學公司製造)0.5 g，製備黏著劑組合物4。 於經剝離處理之聚對苯二甲酸乙二酯膜(三菱樹脂公司製造，DIAFOIL MRV，厚度100 μm)上，以乾燥後之膜厚成為20～30 μm之方式塗敷上述黏接著層用塗敷液後，於80℃下乾燥5分鐘。將其於23℃下固化7天，使交聯劑反應，製成黏著層用片材(β)。 進而，於經剝離處理之聚對苯二甲酸乙二酯膜(三菱樹脂公司製造，DIAFOIL MRQ，厚度75 μm)上，亦同樣地以使黏著劑組合物4乾燥後之膜厚成為20～30 μm之方式塗敷上述黏接著層用塗敷液後，於80℃下乾燥5分鐘。將其於23℃下固化7天，使交聯劑反應，製成黏著層用片材(β')。 將中間層樹脂用片材(α)之兩側之PET膜依序剝離去除，並且將黏著層用樹脂片材(β)及(β')之黏著面依序貼合於中間層用片材(α)之兩表面，製作包含(β)/(α)/(β')之積層體(厚度150 μm)。 隔著殘留於(β)及(β')之表面之PET膜，以波長365 nm之累計光量成為1000 mJ/cm2 、波長405 nm之累計光量成為1400 mJ/cm2 之方式，利用高壓水銀燈照射光，使中間層樹脂用片材(α)進行光交聯，從而製作黏著片積層體3。 [實施例1-4] 使用於加入紫外線吸收劑之PET膜(厚度100 μm)塗佈有聚矽氧脫模劑之脫模膜，代替經剝離處理之聚對苯二甲酸乙二酯膜(DIAFOIL MRV，厚度100 μm)，除此以外，以與實施例1-1相同之方式製成黏著片積層體4。 [實施例1-5] 於實施例1-1中製成之黏著片積層體之聚對苯二甲酸乙二酯膜(DIAFOIL MRV，厚度100 μm)之表面，積層包含微黏著層(5 μm)/聚對苯二甲酸乙二酯膜(25 μm)/紫外線吸收層(3 μm)之表面保護膜之微黏著層面，製成包含脫模膜/黏著片/脫模膜/表面保護膜之構成之黏著片積層體5。 [比較例1-1] 作為光聚合起始劑，代替Esacure KTO46(C-1)而添加Esacure TZT(C-4)15 g，除此以外，以與實施例1-1相同之方式製成黏著片積層體6。 光聚合起始劑(C-4)之405 nm下之吸光係數未達10(mL/(g∙cm))，過低而無法測定。 [比較例1-2] 除不添加紫外線吸收劑(D-2)以外，以與實施例1-2相同之方式製成黏著片積層體7。 [比較例1-3] 對市售之包含丙烯酸系共聚物(A-4，質量平均分子量130萬)之黏著劑溶液(綜研化學公司製造，SK-Dyne1882，固形物成分濃度約17%)1 kg，添加作為異氰酸酯系交聯劑之L-45(B-5)(綜研化學公司製造)1.85 g及作為環氧系交聯劑之E-5XM(B-6)(綜研化學公司製造)0.5 g、作為紫外線吸收劑(D)之2,2'-二羥基-4-甲氧基二苯甲酮(Chemipro Kasei公司製造，Kemisorb111)(D-3)10 g，並均勻混合，製成黏著劑組合物7。 其次，於經剝離處理之聚對苯二甲酸乙二酯膜(三菱樹脂公司製造，DIAFOIL MRV，厚度100 μm)上，以乾燥後之厚度成為50 μm之方式塗佈上述黏著劑組合物後，於80℃下乾燥5分鐘，獲得厚度50 μm之片狀之黏著劑組合物7。 於經剝離處理之聚對苯二甲酸乙二酯膜(三菱樹脂公司製造，DIAFOIL MRQ，厚度75 μm)上，亦同樣地以乾燥後之厚度成為50 μm之方式進行塗佈後，於80℃下乾燥5分鐘，獲得厚度50 μm之片狀之黏著劑組合物7。將該等積層並設為厚度100 μm後，被覆經剝離處理之聚對苯二甲酸乙二酯膜(三菱樹脂公司製造，DIAFOIL MRQ，厚度75 μm)。將其於室溫(23℃)下固化7天，使交聯劑反應，製成黏著片積層體8。 ＜評價＞ [光學特性] 將實施例1-1～1-5及比較例1-1～1-3中製作之黏著片積層體兩側之PET膜依序剝離，以夾入於2片鈉鈣玻璃(厚度0.5 mm)間之方式貼附黏著片，實施高壓釜處理(70℃，表壓0.2 MPa，20分鐘)，進行精貼附。關於黏著片積層體1、2、4、5、6、7，使用介隔UV切割濾光片之高壓水銀燈，以波長405 nm之累計光量成為3000 mJ/cm2 之方式進行光照射，製成光學特性評價用樣品。 藉由分光光度計(島津製作所股份有限公司製造，機器名「UV2450」)測定製成之試片之波長區域360～430 nm下之透光率。 將380 nm下之透光率未達50%者判定為UV吸收性「○(良好)」，將50%以上者判定為UV吸收性「×(較差)」。結果示於表1。 [黏著力] 關於實施例1-1～1-5及比較例1-1～1-3中製作之黏著片，將一脫模膜剝離，並利用手壓輥將作為襯底膜之聚對苯二甲酸乙二酯膜(東洋紡織公司製造，商品名「COSMOSHINE A4300」，厚度100 μm)進行輥壓接。將其裁剪成10 mm寬×100 mm長之短條狀，使用手壓輥將剝離剩餘之脫模膜而露出之黏著面輥貼附於鈉鈣玻璃。實施高壓釜處理(70℃，表壓0.2 MPa，20分鐘)而進行精貼附後，關於黏著片積層體1、2、4、5、6、7，使用介隔UV切割濾光片之高壓水銀燈，以波長405 nm之累計光量成為3000 mJ/cm2 、波長365 nm之累計光量成為5 mJ/cm2 以下之方式照射可見光，製成黏著力測定樣品。 一面將襯底膜以呈180°之角度以剝離速度60 mm/分鐘拉伸，一面自玻璃剝離黏著片，利用荷重元測定拉伸強度，測定黏著片對玻璃之180°剝離強度(N/cm)，於表1中表示為「玻璃接著力」。結果示於表1。 [凹凸吸收性] 對58 mm×110 mm×厚度0.8 mm之玻璃之周緣部(長邊側3 mm，短邊側15 mm)實施厚度20 μm之印刷，準備開口部為52 mm×80 mm之附印刷階差之玻璃板1。 又，對58 mm×110 mm×厚度0.8 mm之玻璃之周緣部(長邊側3 mm，短邊側15 mm)實施厚度10 μm之印刷，準備開口部為52 mm×80 mm之附印刷階差之玻璃板2。 將黏著片積層體之一脫模膜剝離，輥貼合於54 mm×82 mm厚度0.5 mm之鈉鈣玻璃。 其次，將剩餘之脫模膜剝離，於附印刷階差之玻璃板1及2之印刷面，以黏著面之4邊施加於印刷階差之方式使用真空加壓機進行加壓壓接後(絕對壓力5 kPa，溫度70℃，加壓壓力0.04 MPa)，實施高壓釜處理(70℃，表壓0.2 MPa，20分鐘)進行精貼附。關於黏著片積層體1、2、4、5、6、7，自實施了印刷之玻璃側，使用介隔UV切割濾光片之高壓水銀燈，以波長405 nm之累計光量成為3000 mJ/cm2 之方式進行光照射，製成評價用樣品。 關於上述評價用樣品，將可於附20 μm之印刷階差之玻璃板1之階差附近無氣泡等地貼合者判定為凹凸吸收性「◎(優異)」，將關於附10 μm之印刷階差之玻璃板2可於階差附近無氣泡等地貼合者判定為凹凸吸收性「○(良好)」，將關於附印刷階差之玻璃1及2於階差附近看到氣泡者判定為凹凸吸收性「×(較差)」。將結果示於表1。 [耐熱性] 將實施例1-1～1-5及比較例1-1～1-3中製成之黏著片之單面之脫模膜剝離，利用手壓輥於該露出面貼附COP膜(日本瑞翁公司製造，100 μm)。其次，將上述黏著片切成50 mm×80 mm後，剝離剩餘之脫模膜，並利用手壓輥貼附於厚度0.5 mm之鈉鈣玻璃，實施高壓釜處理(溫度80℃，氣壓0.4 MPa，30分鐘)。關於黏著片積層體1、2、4、5、6、7，自COP面，使用介隔UV切割濾光片之高壓水銀燈，以波長405 nm之累計光量成為3000 mJ/cm2 之方式進行光照射，製成評價用樣品。 關於上述評價用樣品，於85℃下固化6小時，將無發泡等且外觀未看到變化者判定為耐熱性「○(良好)」，將看到發泡或剝離者判定為耐熱性「×(較差)」。將結果示於表1。 [耐光性] 將黏著片積層體之一脫模膜剝離，輥貼合於150 mm×200 mm厚度2 mm之鈉鈣玻璃。其次，將剩餘之脫模膜剝離，於露出之黏著面，輥貼合於150 mm×200 mm厚度2 mm之鈉鈣玻璃，實施高壓釜處理(溫度80℃，氣壓0.4 MPa，30分鐘)。 關於黏著片積層體1、2、4、5、6、7，使用高壓水銀燈，以波長405 nm之累計光量成為3000 mJ/cm2 之方式進行光照射，製成評價用樣品。 使用氙耐光性試驗機(Suntest CPS，ATLAS公司製造)對上述評價用樣品照射紫外線24小時，將未於黏著片看到***等者判定為耐光性「○(良好)」，將看到***或剝離者判定為耐光性「×(較差)」。將結果示於表1。 [表1]    實施例1-1 實施例1-2 實施例1-3 實施例1-4 實施例1-5 比較例1-1 比較例1-2 比較例1-3 中間層 接著層 丙烯酸系共聚物 A-1 100          100 100 100       A-2    100                100    A-3       100                   A-4          100             100 交聯劑 B-1 10          10 10 10       B-2    5                5    B-3       20                   L-45          1.85             1.85 E-5XM          0.5             0.5 光起始劑 C-1 1.5          1.5 1.5          C-2    1                1    C-3       0.7                   C-4                   1.5       UV吸收劑 D-1 0.5          0.5 0.5 0.5       D-2    2                      D-3       1                1 備註       積層構成 UV切割PET UV切割保護膜          光起始劑 吸光係數(405 nm) mL/(g∙cm) 7.4×101 1.6×102 9.0×102 7.4×101 7.4×101 ＜10 1.6×102 - 玻璃接著力 N/cm 8 4 10 8 8 2 4 5 黏著片透光率(%) 350 nm 0 0 0 0 0 0 80 0 360 nm 1 0 0 1 1 1 84 0 370 nm 11 2 0 11 11 11 86 0 380 nm 44 17 3 44 44 44 86 1 390 nm 71 55 19 71 71 71 88 13 400 nm 81 77 51 81 81 81 88 42 410 nm 87 86 77 87 87 87 89 73 420 nm 89 89 87 89 89 89 89 86 430 nm 89 89 89 89 89 89 89 89 UV吸收性 〇 〇 〇 〇 〇 〇 × 〇 貼合可靠性 凹凸吸收性 ◎ ◎ 〇 ◎ ◎ ◎ ◎ × 耐熱性 〇 〇 〇 〇 〇 × 〇 〇 耐光性 〇 〇 〇 〇 〇 〇 × 〇 綜合評價 〇 〇 〇 〇 〇 〇 × × 關於實施例1-1中使用之經剝離處理之聚對苯二甲酸乙二酯膜(三菱樹脂公司製造，DIAFOIL MRV，厚度100 μm)、實施例1-4中使用之於加入紫外線吸收劑之PET膜(厚度100 μm)塗佈有聚矽氧脫模劑之脫模膜、及實施例1-5中使用之表面保護膜，藉由分光光度計(島津製作所股份有限公司製造，機器名「UV2450」)測定波長區域380～450 nm之透光率。結果示於表2。 關於黏著片積層體1、黏著片積層體4及黏著片積層體5，分別以經剝離處理之聚對苯二甲酸乙二酯膜(三菱樹脂公司製造，DIAFOIL MRV，厚度100 μm)、實施例1-4中使用之於加入紫外線吸收劑之PET膜(厚度100 μm)塗佈有聚矽氧脫模劑之脫模膜及表面保護膜側朝上之方式靜置。自該膜側照射螢光燈(照度1100Lx)之光7天。照射之光之波長405 nm下之累計光量約為43 J/cm2 ，波長365 nm下之累計光量約為1 mJ/cm2 以下，無法測定。 關於光照射處理前後之黏著片積層體1及4，藉由以下方法求出黏著材之凝膠分率。結果示於表2。 1)稱量黏著劑組合物(W1)，包裹於預先測得重量之SUS絲網(W0)。 2)將上述SUS絲網浸漬於100 mL之乙酸乙酯中24小時。 3)取出SUS絲網，於75℃下半乾燥4小時。 4)求出乾燥後之重量(W2)，根據下述式測定黏著劑組合物之凝膠分率。 凝膠分率(%)＝100×(W2－W0)/W1 關於保管穩定性，將凝膠分率之變化於螢光燈照射前後未達5點者判定為「○(良好)」，將光照射後凝膠分率增加5點以上者判定為「×(較差)」。將結果示於表2。 [表2]    實施例1-1 實施例1-4 實施例1-5 脫模PET 透光率(%) 380 nm 84 26 0 390 nm 85 33 0 400 nm 86 23 0 410 nm 86 13 1 420 nm 87 5 9 430 nm 87 3 39 440 nm 88 2 69 450 nm 88 1 81 凝膠分率 光照射前 0% 0% 0% 光照射後 68% 2% 0% 保管穩定性 × 〇 〇 實施例1-1～1-5之黏著片積層體係不僅具有優異之紫外線吸收性能，而且具有兼顧到貼合時之凹凸吸收性或構件貼合後之可靠性之優異品質者。 相對於此，比較例1-1係使用波長405 nm下之吸光係數未達10 mL/(g∙cm)之光聚合起始劑，因此亦即未使用波長405 nm下之吸光係數為10 mL/(g∙cm)以上之光聚合起始劑，因此即便進行光照射，黏著材亦不會硬化，無法獲得2次貼附後之黏著力或貼合後之可靠性。 比較例1-2不含紫外線吸收劑(D)，無法獲得紫外線吸收性能。因此，於耐光性試驗中看到黏著片之發泡，貼合可靠性較差。 比較例1-3係藉由熱交聯而使黏著材組合物交聯之黏著片。由於不具有光硬化性層，故而貼合時之凹凸吸收性較差。 又，實施例1-4係使用加入紫外線吸收劑之PET膜作為脫模膜。藉此，可抑制貼合於構件前黏著材組合物之光硬化反應進行，可製成保管穩定性優異之黏著片積層體。 又，實施例1-5係於脫模膜之表面積層具有紫外線吸收層之表面保護膜。藉此，可抑制貼合於構件前黏著材組合物之光硬化反應進行，可製成保管穩定性優異之黏著片積層體。 以下，藉由實施例2-1～2-3及比較例2-1～2-2進一步詳細地進行說明。 但是，本發明並不限定於該等。再者，下述實施例及比較例中使用之各層之黏著樹脂組合物之組成示於表3。 [實施例2-1] 對作為(甲基)丙烯酸系共聚物(2-A)之包含(甲基)丙烯酸2-乙基己酯76質量份、乙酸乙烯酯20質量份、丙烯酸4質量份之共聚物(2-A-1，質量平均分子量40萬)1 kg，添加作為交聯劑(2-B)之丙氧化季戊四醇四丙烯酸酯(新中村化學公司製造，ATM-4P)(2-B-1)200 g、作為光聚合起始劑(2-C)之Irgacure 369(2-C-1)(BASF公司製造)8 g、作為紫外線吸收劑(2-D)之2,2'-二羥基-4-甲氧基二苯甲酮(Chemipro Kasei公司製造，Kemisorb111)(2-D-1)10 g，並均勻混合，獲得黏著樹脂組合物2-1。 光聚合起始劑(2-C-1)之405 nm下之吸光係數為1.6×102 mL/(g∙cm)。 以經剝離處理之2片聚對苯二甲酸乙二酯膜(三菱樹脂公司製造，DIAFOIL MRF，厚度75 μm/三菱樹脂公司製造，DIAFOIL MRT，厚度38 μm)夾著黏著樹脂組合物2-1，並以厚度成為110 μm之方式賦形為片狀，製成中間層用片材(α-1)。 對市售之包含丙烯酸系共聚物(2-A-2，質量平均分子量130萬)之黏著劑溶液(綜研化學公司製造，SK-Dyne1882，固形物成分濃度約17%)1 kg，添加作為異氰酸酯系交聯劑之L-45(2-B-2)(綜研化學公司製造)1.85 g及作為環氧系交聯劑之E-5XM(2-B-3)(綜研化學公司製造)0.5 g，製備黏著樹脂組合物2。於經剝離處理之聚對苯二甲酸乙二酯膜(三菱樹脂公司製造，DIAFOIL MRV，厚度100 μm)上，以乾燥後之厚度成為20 μm之方式塗敷上述黏接著層用塗敷液後，於80℃下乾燥5分鐘而使β層熱硬化，製成表層用片材(β-1)。 進而，於經剝離處理之聚對苯二甲酸乙二酯膜(三菱樹脂公司製造，DIAFOIL MRQ，厚度75 μm)上，亦同樣地，以乾燥後之厚度成為20 μm之方式塗敷黏著樹脂組合物2後，於80℃下乾燥5分鐘而使β層熱硬化，製成表層用片材(β'-1)。 將中間層用片材(α-1)兩側之PET膜依序剝離去除，並且將表層用片材(β-1)及(β'-1)之黏著面依序貼合於兩表面，製作包含(β-1)/(α-1)/(β'-1)之積層體。 隔著殘留於(β-1)及(β'-1)之表面之PET膜，以波長405 nm之累計光量成為1500 mJ/cm2 之方式使用高壓水銀燈進行照射，使α層硬化，製作透明雙面黏著片積層體2-1(厚度150 μm)。 [實施例2-2] 對(甲基)丙烯酸系共聚物(2-A-1)1 kg添加交聯劑(2-B-1)200 g、作為光聚合起始劑(2-C)之Esacure KTO46(2-C-2)(Lanberti公司製造)20 g、紫外線吸收劑(2-D-1)20 g並均勻混合，獲得黏著樹脂組合物2-3。 光聚合起始劑(2-C-2)之405 nm下之吸光係數為7.4×101 mL/(g∙cm)。 以經剝離處理之2片聚對苯二甲酸乙二酯膜(三菱樹脂公司製造，DIAFOIL MRF，厚度75 μm/三菱樹脂公司製造，DIAFOIL MRT，厚度38 μm)夾著黏著樹脂組合物2-3，並以厚度成為60 μm之方式賦形為片狀，製成中間層用片材(α-2)。 與實施例2-1同樣地，將中間層用片材(α-2)兩側之PET膜依序剝離去除，並且將表層用片材(β-1)及(β'-1)之黏著面依序貼合於兩表面，製作包含(β-1)/(α-2)/(β'-1)之積層體。 隔著殘留於(β-1)及(β'-1)之表面之PET膜，以波長405 nm之累計光量成為3000 mJ/cm2 之方式使用高壓水銀燈進行照射，使α層硬化，製作透明雙面黏著片積層體2-2(厚度100 μm)。 [實施例2-3] 對(甲基)丙烯酸系共聚物(2-A-1)1 kg添加交聯劑(2-B-1)200 g、光聚合起始劑(2-C-2)8 g、紫外線吸收劑(2-D-1)20 g，並均勻混合，獲得黏著樹脂組合物2-4。 以經剝離處理之2片聚對苯二甲酸乙二酯膜(三菱樹脂公司製造，DIAFOIL MRF，厚度75 μm/三菱樹脂公司製造，DIAFOIL MRT，厚度38 μm)夾著黏著樹脂組合物2-4，並以厚度成為60 μm之方式賦形為片狀，製成中間層用片材(α-3)。 與實施例2-1同樣地，將中間層用片材(α-3)兩側之PET膜依序剝離去除，並且將表層用片材(β-1)及(β'-1)之黏著面依序貼合於雙面，製作包含(β-1)/(α-3)/(β'-1)之積層體。 隔著殘留於(β-1)及(β'-1)之表面之PET膜，以波長405 nm之累計光量成為3000 mJ/cm2 之方式使用高壓水銀燈進行照射，使α層硬化，製作透明雙面黏著片積層體2-3(厚度100 μm)。 [比較例2-1] 對(甲基)丙烯酸系共聚物(2-A-1)1 kg，添加交聯劑(2-B-1)200 g、作為光聚合起始劑(2-C)之Esacure TZT(2-C-3)(Lanberti公司製造)10 g、作為紫外線吸收劑(2-D)之2,2'-二羥基-4-甲氧基二苯甲酮(Chemipro Kasei公司製造，Kemisorb111)(2-D-1)20 g，並均勻混合，獲得黏著樹脂組合物2-5。 光聚合起始劑(2-C-3)之405 nm下之吸光係數未達10 mL/(g∙cm)，過低而無法測定。 以經剝離處理之2片聚對苯二甲酸乙二酯膜(三菱樹脂公司製造，DIAFOIL MRF，厚度75 μm/三菱樹脂公司製造，DIAFOIL MRT，厚度38 μm)夾著黏著樹脂組合物2-5，並以厚度成為110 μm之方式賦形為片狀，製成中間層用片材(α-4)。 與實施例2-1同樣地，將中間層用片材(α-4)兩側之PET膜依序剝離去除，並且將表層用片材(β-1)及(β'-1)之黏著面依序貼合於兩表面，製作包含(β-1)/(α-4)/(β'-1)之積層體。 隔著殘留於(β-1)及(β'-1)之表面之PET膜，以波長405 nm之累計光量成為1500 mJ/cm2 之方式使用高壓水銀燈進行照射，使α層硬化，製作透明雙面黏著片積層體2-4(厚度100 μm)。 [比較例2-2] 對(甲基)丙烯酸系共聚物(2-A-1)1 kg，添加交聯劑(2-B-1)200 g、光聚合起始劑(2-C-2)8 g並均勻混合，獲得黏著樹脂組合物2-6。此時，未添加紫外線吸收劑(2-D)。 以經剝離處理之2片聚對苯二甲酸乙二酯膜(三菱樹脂公司製造，DIAFOIL MRF，厚度75 μm/三菱樹脂公司製造，DIAFOIL MRT，厚度38 μm)夾著黏著樹脂組合物2-6，並以厚度成為110 μm之方式賦形為片狀，製成中間層用片材(α-5)。 與實施例2-1同樣地，將中間層用片材(α-5)兩側之PET膜依序剝離去除，並且將表層用片材(β-1)及(β'-1)之黏著面依序貼合於兩表面，製作包含(β-1)/(α-5)/(β'-1)之積層體。 隔著殘留於(β-1)及(β'-1)之表面之PET膜，以波長405 nm之累計光量成為1500 mJ/cm2 之方式使用高壓水銀燈進行照射，使α層硬化，製作透明雙面黏著片積層體2-5(厚度150 μm)。 ＜評價＞ [紫外線吸收性能] 將實施例2-1～2-3及比較例2-1～2-2中製作之透明雙面黏著片積層體之兩側之PET膜依序剝離，以夾入於2片鈉鈣玻璃(54×82 mm，厚度0.5 mm)間之方式貼附黏著片後，實施高壓釜處理(70℃，表壓0.2 MPa，20分鐘)進行精貼附，作為紫外線吸收性能評價用樣品。 藉由分光光度計(島津製作所股份有限公司製造，機器名「UV2450」)測定所製成之試片之波長區域360～430 nm下之透光率。將380 nm下之透光率未達50%者判定為「○(良好)」，將50%以上者判定為「×(較差)」。結果示於表4。 [玻璃接著力] 關於實施例2-1～2-3及比較例2-1～2-2中製作之透明雙面黏著片，剝離一剝離膜，利用手壓輥將作為襯底膜之聚對苯二甲酸乙二酯膜(東洋紡織公司製造，商品名「COSMOSHINE A4300」，厚度100 μm)進行輥壓接。將其裁剪成10 mm寬×100 mm長之短條狀，使用手壓輥將剝離剩餘之剝離膜而露出之黏著面輥貼附於鈉鈣玻璃。對其實施高壓釜處理(70℃，表壓0.2 MPa，20分鐘)而進行精貼附，製成黏著力測定樣品。一面將襯底膜以呈180°之角度以剝離速度60 mm/分鐘進行拉伸，一面自玻璃剝離黏著片，藉由荷重元測定拉伸強度，測定黏著片對玻璃之180°剝離強度，結果示於表4。 [保持力(偏移長度)] 將實施例2-1～2-3及比較例2-1～2-2中製作之黏著片裁剪成50 mm×100 mm後，將單面之剝離膜剝離，以該黏著片之單面重疊於襯底用聚對苯二甲酸乙二酯膜(厚度38 μm)之方式利用手壓輥進行貼附，將其裁剪成寬25 mm×長度100 mm之短條狀而作為試片。其次，將殘留之剝離膜剝離，將試片以對垂直地豎立設置之SUS板(厚度120 mm，5 mm×1.5 mm)重疊20 mm之長度之方式藉由手壓輥進行貼附。此時，透明雙面黏著片與SUS板之貼附面積成為25 mm×20 mm。 其後，使試片於40℃之氛圍下固化15分鐘後，對試片沿垂直方向安裝並施加荷重500 g之砝碼，靜置30分鐘後，測定SUS與試片之貼附位置向下方之偏移長度( mm)。 將偏移長度未達1 mm者判定為「◎(優異)」，將偏移長度為1 mm以上且未達2 mm者判定為「〇(良好)」，將偏移長度為2 mm以上者判定為「×(較差)」。將結果示於表4。 [耐發泡可靠性] 作為耐發泡可靠性評價用樣品，使用2片與紫外線吸收性能評價用樣品相同者。將其於85℃下固化100小時，將無發泡等且外觀未看到變化者判定為「○(良好)」，將看到發泡或剝離者判定為「×(較差)」。將結果示於表4。 [表3] 黏著樹脂組成物 2-1 2-2 2-3 2-4 2-5 2-6 (甲基)丙烯酸系共聚物(A) A-1 100    100 100 100 100 A-2    100             交聯劑(B) B-1 20    20 20 20 20 B-2    0.185             B-3    0.05             光聚合起始劑(C) C-1 0.8             0.8 C-2       2 0.8       C-3             1    紫外線吸收劑(D) D-1 1    2 2 2    光聚合起始劑(C) 吸光係數 405 nm 1.6×102 - 7.4×101 7.4×101 ＜10 1.6×102 [表4]    實施例2-1 實施例2-2 實施例2-3 比較例2-1 比較例2-2 透光率[%] 360 nm 0 0 0 0 84 370 nm 0 0 0 0 85 380 nm 3 4 3 3 88 390 nm 19 21 18 20 88 400 nm 51 53 52 53 89 410 nm 77 78 78 79 89 420 nm 87 87 87 88 89 430 nm 89 89 89 89 89 紫外線吸收性能 〇 〇 〇 〇 × 玻璃接著力[N/cm] 10 9 10 2 7 保持力(40℃) ◎ (1 mm) ◎ (1 mm) 〇 (1.9 mm) × (落下) ◎ (＜1 mm) 耐發泡可靠性 〇 〇 〇 × 〇 綜合評價 ◎ ◎ 〇 × × 對實施例2-1～2-3之黏著片積層體進行觀察，結果未觀察到紫外線吸收劑(D)之滲出。 實施例2-1～2-3之黏著片積層體係維持黏著力或保持力、耐濕熱可靠性等特性並且賦予優異之紫外線吸收性能者。 比較例2-1由於使用波長405 nm之吸光係數未達10 mL/(g∙cm)之光聚合起始劑，故而即便進行光照射，黏著劑亦不會硬化，黏著力或貼合後之可靠性較差。 比較例2-2由於α層不含紫外線吸收劑(D)，故而紫外線吸收性能較差。Hereinafter, an example of an embodiment of the present invention will be described in detail. However, the present invention is not limited to the following embodiments. <This adhesive sheet> A transparent double-sided adhesive sheet as an example of an embodiment of the present invention contains a (meth)acrylic copolymer (A), a cross-linking agent (B), and an absorbance coefficient of 10 mL at a wavelength of 405 nm. A transparent double-sided adhesive sheet (called " This adhesive sheet"). [(Meth)acrylic copolymer (A)] The (meth)acrylic polymer as the base polymer of this adhesive sheet can be polymerized by using an acrylic monomer or a methacrylic monomer. Characteristics such as glass transition temperature (Tg) can be appropriately adjusted according to the type of body, composition ratio, and polymerization conditions. The so-called "base polymer" in this adhesive sheet refers to the resin that is the main component of this adhesive sheet. It does not specify a specific content. As a standard, it is a resin occupying 50 mass % or more, especially 65 mass % or more, especially 80 mass % or more (including 100 mass %) of the resin contained in this adhesive sheet. In addition, when there are two or more types of base polymers, the total amount thereof corresponds to the above-mentioned content. Examples of the (meth)acrylic (co)polymer (A) include, in addition to the homopolymer of (meth)acrylic acid alkyl ester, those obtained by polymerizing it with a copolymerizable monomer component. More preferably, the copolymer contains alkyl (meth)acrylate and is selected from the group consisting of carboxyl group-containing monomers, hydroxyl group-containing monomers, amine group-containing monomers, epoxy group-containing monomers, and copolymerizable copolymers therewith. A copolymer containing any one or more monomers such as amide-based monomers and other vinyl monomers as monomer components. More specifically, those containing linear or branched (meth)acrylic acid alkyl esters having 4 to 18 carbon atoms in the side chain (hereinafter also referred to as "copolymerizable monomer A") and copolymerizable therewith can be cited. Carboxyl group-containing monomer (hereinafter also referred to as "copolymerizable monomer B"), vinyl monomer (hereinafter also referred to as "copolymerizable monomer C"), and side chain carbon number of 1 to 3 (methyl) A copolymer of one or more monomers including acrylate (hereinafter also referred to as "copolymerizable monomer D") and a hydroxyl-containing monomer (hereinafter referred to as "copolymerizable monomer E"). Furthermore, particularly preferred examples include: (a) a copolymer containing a monomer component containing copolymerizable monomer A, copolymerizable monomer B and/or copolymerizable monomer C, or (b) a copolymer containing A copolymer of monomer components of copolymerizable monomer A, copolymerizable monomer B and/or copolymerizable monomer C, and copolymerizable monomer D and/or copolymerizable monomer E. Specifically, copolymers of copolymerizable monomers A and B, copolymers of copolymerizable monomers A and C, copolymers of copolymerizable monomers A, B, and C, copolymers of copolymerizable monomers A, B, and Copolymers of D, copolymers of comonomers A, B and E, copolymers of comonomers A, B, D and E, copolymers of comonomers A, C and D, comonomers Copolymers of A, C and E, copolymers of comonomers A, C, D and E, copolymers of comonomers A, B, C and D, copolymers of comonomers A, B, C and E copolymer, copolymer of copolymerizable monomers A, B, C, D and E. Examples of the "copolymerizable monomer A" include (n-butylmeth)acrylate, isobutyl(meth)acrylate, second-butyl(meth)acrylate, and third-butyl(meth)acrylate. Ester, amyl (meth)acrylate, isopentyl (meth)acrylate, neopentyl (meth)acrylate, hexyl (meth)acrylate, cyclohexyl (meth)acrylate, (meth)acrylic acid Heptyl ester, 2-ethylhexyl (meth)acrylate, n-octyl (meth)acrylate, isooctyl (meth)acrylate, nonyl (meth)acrylate, isononyl (meth)acrylate, tert-Butylcyclohexyl (meth)acrylate, decyl (meth)acrylate, isodecyl (meth)acrylate, undecyl (meth)acrylate, lauryl (meth)acrylate, ( Tridecyl methacrylate, myristyl (meth)acrylate, cetyl (meth)acrylate, stearyl (meth)acrylate, isostearyl (meth)acrylate, ( Isopropyl methacrylate, 3,5,5-trimethylcyclohexane (meth)acrylate, dicyclopentyl (meth)acrylate, dicyclopentenyl (meth)acrylate, (meth)acrylate base) dicyclopentenyloxyethyl acrylate, etc. These can also be used 1 type or in combination of 2 or more types. The above-mentioned copolymerizable monomer A is preferably contained in the range of 30 mass% or more and 90 mass% or less in all monomer components of the copolymer, and more preferably, it is contained in the range of 35 mass% or more or 88 mass% or less, especially Furthermore, it is more preferable that it is contained in the range of 40 mass % or more or 85 mass % or less. Examples of the "copolymerizable monomer B" include: (meth)acrylic acid, 2-(meth)acryloxyethylhexahydrophthalic acid, and 2-(meth)acryloxypropyl Hexahydrophthalic acid, 2-(meth)acryloxyethyl phthalic acid, 2-(meth)acryloxypropylphthalic acid, 2-(meth)acryloxyethyl Maleic acid, 2-(meth)acryloxypropylmaleic acid, 2-(meth)acryloxyethylsuccinic acid, 2-(meth)acryloxypropyl Succinic acid, crotonic acid, fumaric acid, maleic acid, itaconic acid. These may be used 1 type or in combination of 2 or more types. Furthermore, the meaning of "(meth)acrylic acid" includes acrylic acid and methacrylic acid. Likewise, the meaning of "(meth)acrylyl" includes both acrylyl and methacrylyl. Examples of the "copolymerizable monomer C" include compounds having a vinyl group in the molecule. Examples of such compounds include (meth)acrylic acid alkyl esters whose alkyl group has 1 to 12 carbon atoms; and those having functional groups such as hydroxyl group, amide group, and alkoxyalkyl group in the molecule. Monomers; and polyalkylene glycol di(meth)acrylates; and vinyl ester monomers such as vinyl acetate, vinyl propionate, and vinyl laurate; and styrene, chlorostyrene, chloromethyl Aromatic vinyl monomers such as styrene, α-methylstyrene and other substituted styrenes. These may be used 1 type or in combination of 2 or more types. The above-mentioned copolymerizable monomer B and the above-mentioned copolymerizable monomer C are preferably contained in the range of 1.2 mass% to 15 mass% or less in all monomer components of the copolymer. From the viewpoint of obtaining excellent adhesive properties, The content is preferably in the range of 1.5% by mass or more and 10% by mass or less, and particularly preferably the content is in the range of 2% by mass or more or 8% by mass or less. Examples of the "copolymerizable monomer D" include methyl (meth)acrylate, ethyl (meth)acrylate, n-propyl (meth)acrylate, isopropyl (meth)acrylate, and the like. These may be used 1 type or in combination of 2 or more types. The copolymerizable monomer D is preferably contained in the range of 0 mass % or more and 70 mass % or less in all monomer components of the copolymer, and more preferably in the range of 3 mass % or more or 65 mass % or less, especially Furthermore, it is more preferable that it is contained in the range of 5 mass % or more or 60 mass % or less. Examples of the "copolymerizable monomer E" include: (2-hydroxyethylmeth)acrylate, 2-hydroxypropyl(meth)acrylate, 3-hydroxypropyl(meth)acrylate, (meth)acrylate (meth)acrylic acid hydroxyalkyl esters such as 2-hydroxybutyl acrylate. These may be used 1 type or in combination of 2 or more types. The above-mentioned copolymerizable monomer E is preferably contained in the range of 0 mass % or more and 30 mass % or less in all monomer components of the copolymer, and more preferably, it is contained in the range of 0 mass % or more or 25 mass % or less, especially Furthermore, it is more preferable that it is contained in the range of 0 mass % or more and 20 mass % or less. In addition to those disclosed above, acid anhydride group-containing monomers such as maleic anhydride and itaconic anhydride, glycidyl (meth)acrylate, α-ethyl glycidyl acrylate, and (meth)acrylic acid can also be used appropriately if necessary. Epoxy group-containing monomers such as 3,4-epoxybutyl ester, (meth)acrylic acid dimethylaminoethyl, (meth)acrylic acid diethylaminoethyl and other amine group-containing (methyl) Acrylate monomers, (meth)acrylamide, N-tert-butyl(meth)acrylamide, N-hydroxymethyl(meth)acrylamide, N-methoxymethyl(meth)acrylamide acrylamide, N-butoxymethyl(meth)acrylamide, diacetone(meth)acrylamide, maleicamide, maleimide, etc. contain amide groups Monomers include vinylpyrrolidone, vinylpyridine, vinylcarbazole and other heterocyclic basic monomers. Specific examples of (meth)acrylic (co)polymers include: 2-ethylhexyl (meth)acrylate, octyl (meth)acrylate, decyl (meth)acrylate, Monomer components (a) such as lauryl methacrylate, isostearyl (meth)acrylate, butyl (meth)acrylate, ethyl (meth)acrylate, and methyl (meth)acrylate have carboxyl groups (meth)acrylic acid, 2-(meth)acryloxyethylhexahydrophthalic acid, 2-(meth)acryloxypropylhexahydrophthalic acid, 2-(meth)propylene Hydroxyethylphthalic acid, 2-(meth)acryloyloxypropylphthalic acid, 2-(meth)acryloyloxyethylmaleic acid, 2-(meth)propylene Hydroxypropylmaleic acid, 2-(meth)acryloyloxyethylsuccinic acid, 2-(meth)acryloyloxypropylsuccinic acid, crotonic acid, fumaric acid , maleic acid, itaconic acid and other monomer components (b), and hydroxyethyl (meth)acrylate, hydroxypropyl (meth)acrylate, hydroxybutyrate (meth)acrylate with organic functional groups, etc. Ester, glyceryl (meth)acrylate, monomethyl maleate, monomethyl itaconate, vinyl acetate, glycidyl (meth)acrylate, (meth)acrylamide, (methyl) (meth)acrylate copolymer obtained by copolymerizing monomer components (c) such as acrylonitrile, fluorinated (meth)acrylate, and (meth)acrylic polysiloxyester. The mass average molecular weight of the (meth)acrylic (co)polymer is preferably 100,000 to 1,500,000, preferably 150,000 or more or 1,300,000 or less, and particularly preferably 200,000 or more or 1,200,000 or less. When it is desired to obtain an adhesive composition with higher cohesive force, from the viewpoint that the larger the molecular weight, the more cohesive force can be obtained through the entanglement of molecular chains, the mass average molecular weight is preferably 700,000 to 1.5 million, especially It is above 800,000 or below 1.3 million. On the other hand, when it is desired to obtain an adhesive composition with high fluidity or stress relaxation properties, the mass average molecular weight is preferably 70,000 to 700,000, and more preferably 100,000 or more or 600,000 or less. In addition, when a solvent is not used for molding an adhesive sheet etc., it is difficult to use a polymer with a relatively large molecular weight. Therefore, the mass average molecular weight of the acrylic copolymer is preferably 70,000 to 700,000, and more preferably 100,000 or more or 60,000. Less than 10,000, especially preferably more than 150,000 or less than 500,000. (Acrylic copolymer (A1)) An example of a preferred base polymer of this adhesive sheet is a (meth)acrylic copolymer (A1) containing a graft copolymer having a macromonomer as a branch component. . As long as the above-mentioned acrylic copolymer (A1) is used as the base resin to constitute the adhesive sheet, the adhesive sheet can maintain the sheet shape at room temperature and exhibit self-adhesiveness. If heated in an uncrosslinked state, the adhesive sheet will have melting or The fluid hot-meltability can further allow it to be photohardened, and it can exert excellent cohesive force for adhesion after photohardening. Therefore, as long as the acrylic copolymer (A1) is used as the base polymer of this adhesive sheet, even in an uncrosslinked state, it can have the following properties, that is, it can exhibit adhesiveness at room temperature (20°C), and The property of softening or fluidizing at 100°C, or the property of softening or fluidizing when heated to a temperature of 50 to 90°C, preferably above 60°C or below 80°C. The glass transition temperature of the copolymer constituting the dry component of the acrylic copolymer (A1) is preferably -70 to 0°C. At this time, the glass transition temperature of the copolymer component constituting the dry component refers to the glass transition temperature of the polymer obtained by copolymerizing only the monomer components constituting the dry component of the acrylic copolymer (A1). Specifically, it means the value calculated by Fox's calculation formula of the glass transition temperature and the composition ratio of the polymer obtained from the homopolymer of each component of the copolymer. In addition, the calculation formula of Fox refers to the calculated value obtained by the following formula, and can be obtained using the value described in the Polymer Handbook [Polymer Handbook, J. Brandrup, Interscience, 1989]. 1/(273+Tg)=Σ(Wi/(273+Tgi)) [In the formula, Wi represents the weight fraction of monomer i, and Tgi represents the Tg (℃) of the homopolymer of monomer i] The above-mentioned acrylic copolymer ( The glass transition temperature of the copolymer component of A1) will affect the softness of the adhesive sheet at room temperature or the wettability and adhesion of the adhesive sheet to the adherend. Therefore, in order to make this adhesive sheet The adhesive sheet obtains moderate adhesion (tackiness) at room temperature. The glass transition temperature is preferably -70°C to 0°C, particularly preferably above -65°C or below -5°C, particularly preferably - Above 60℃ or below -10℃. However, even if the glass transition temperatures of the copolymer components are set to the same temperature, the viscoelasticity can be adjusted by adjusting the molecular weight. For example, the copolymer component can be made softer by reducing its molecular weight. Examples of the (meth)acrylate monomer contained in the dry component of the acrylic copolymer (A1) include: (meth)acrylic acid methyl ester, (meth) ethyl acrylate, and (meth) propyl acrylate. , Isopropyl (meth)acrylate, n-butyl (meth)acrylate, isobutyl (meth)acrylate, second butyl (meth)acrylate, third butyl (meth)acrylate, (meth)acrylate (Basic) amyl acrylate, isopentyl (meth)acrylate, neopentyl (meth)acrylate, hexyl (meth)acrylate, cyclohexyl (meth)acrylate, heptyl (meth)acrylate, ( 2-ethylhexyl methacrylate, n-octyl acrylate, isooctyl acrylate, nonyl (meth)acrylate, isononyl (meth)acrylate, tert-butylcyclohexyl (meth)acrylate , decyl (meth)acrylate, isodecyl (meth)acrylate, undecyl (meth)acrylate, lauryl (meth)acrylate, cetyl (meth)acrylate, (meth) Stearyl acrylate, isostearyl (meth)acrylate, behenyl acrylate, isocyanate (meth)acrylate, 2-phenoxyethyl (meth)acrylate, 3,5,5-trimethyl cyclohexane acrylate, p-cumylphenol EO modified (meth)acrylate, dicyclopentyl (meth)acrylate, dicyclopentenyl (meth)acrylate, dicyclopentyl (meth)acrylate Cyclopentenyloxyethyl ester, benzyl (meth)acrylate, etc. Among these, hydroxyethyl (meth)acrylate, hydroxypropyl (meth)acrylate, hydroxybutyl (meth)acrylate, and glycerin (meth)acrylate having hydrophilic groups or organic functional groups can also be used. (meth)acrylates containing hydroxyl groups such as esters, or (meth)acrylic acid, 2-(meth)acryloxyethylhexahydrophthalic acid, 2-(meth)acryloxypropylhexahydrophthalic acid Hydrophthalic acid, 2-(meth)acryloxyethylphthalic acid, 2-(meth)acryloxypropylphthalic acid, 2-(meth)acryloxyethyl cis Butenedioic acid, 2-(meth)acryloxypropylmaleic acid, 2-(meth)acryloxyethylsuccinic acid, 2-(meth)acryloxypropyl Succinic acid, crotonic acid, fumaric acid, maleic acid, itaconic acid, maleic acid monomethyl ester, itonic acid monomethyl ester and other carboxyl group-containing monomers, maleic anhydride, Anhydride group-containing monomers such as Iconic anhydride, epoxy group-containing monomers such as glycidyl (meth)acrylate, α-ethyl acrylate, 3,4-epoxybutyl (meth)acrylate, etc. Amino group-containing (meth)acrylate monomers such as dimethylaminoethyl methacrylate and diethylaminoethyl (meth)acrylate, (meth)acrylamide, N-th Tributyl(meth)acrylamide, N-hydroxymethyl(meth)acrylamide, N-methoxymethyl(meth)acrylamide, N-butoxymethyl(methyl) Monomers containing amide groups such as acrylamide, diacetone acrylamide, maleimide, maleimide, etc., heterocyclic rings such as vinylpyrrolidone, vinylpyridine, vinylcarbazole, etc. It is an alkaline monomer, etc. In addition, styrene, tert-butylstyrene, α-methylstyrene, vinyltoluene, acrylonitrile, and methacrylene that can be copolymerized with the above-mentioned acrylic monomer or methacrylic monomer can also be used appropriately. Nitrile, vinyl acetate, vinyl propionate, alkyl vinyl ether, hydroxyalkyl vinyl ether, alkyl vinyl monomer and other vinyl monomers. Moreover, the dry component of the acrylic copolymer (A1) preferably contains a hydrophobic (meth)acrylate monomer and a hydrophilic (meth)acrylate monomer as structural units. If the dry component of the acrylic copolymer (A1) consists only of hydrophobic monomers, it is considered that there is a tendency for moist heat whitening. Therefore, it is preferable to introduce hydrophilic monomers into the dry component to prevent moist heat whitening. Specifically, examples of the dry components of the acrylic copolymer (A1) include hydrophobic (meth)acrylate monomers, hydrophilic (meth)acrylate monomers, and terminal macromolecular monomers. A copolymer component formed by random copolymerization of polymerizable functional groups. Here, examples of the hydrophobic (meth)acrylate monomer include: (n-butylmeth)acrylate, isobutyl(meth)acrylate, second-butyl(meth)acrylate, (meth)acrylate Tert-butyl methacrylate, amyl (meth)acrylate, isopentyl (meth)acrylate, neopentyl (meth)acrylate, hexyl (meth)acrylate, cyclohexyl (meth)acrylate Ester, heptyl (meth)acrylate, 2-ethylhexyl (meth)acrylate, n-octyl acrylate, isooctyl acrylate, nonyl (meth)acrylate, isononyl (meth)acrylate, ( tert-butylcyclohexyl methacrylate, decyl (meth)acrylate, isodecyl (meth)acrylate, undecyl (meth)acrylate, lauryl (meth)acrylate, (meth)acrylate Cetyl acrylate, stearyl (meth)acrylate, isostearyl (meth)acrylate, behenyl acrylate, isopropyl (meth)acrylate, cyclohexyl (meth)acrylate, ( Dicyclopentenoxyethyl methacrylate, methyl methacrylate. Examples of the hydrophobic vinyl monomer include vinyl acetate, styrene, tert-butylstyrene, α-methylstyrene, vinyltoluene, alkylvinyl monomers, and the like. Examples of the hydrophilic (meth)acrylate monomer include: methyl acrylate, (meth)acrylic acid, tetrahydrofurfuryl (meth)acrylate, or hydroxyethyl (meth)acrylate, (meth)acrylate, Hydroxypropyl acrylate, hydroxybutyl (meth)acrylate, glyceryl (meth)acrylate and other hydroxyl-containing (meth)acrylates, or (meth)acrylic acid, 2-(meth)acryloxy Ethylhexahydrophthalic acid, 2-(meth)acryloxypropylhexahydrophthalic acid, 2-(meth)acryloxyethylphthalic acid, 2-(meth)propylene Hydroxypropylphthalic acid, 2-(meth)acryloyloxyethylmaleic acid, 2-(meth)acryloyloxypropylmaleic acid, 2-(methyl) ) Acryloxyethylsuccinic acid, 2-(meth)acryloxypropylsuccinic acid, crotonic acid, fumaric acid, maleic acid, itaconic acid, maleic acid Carboxyl group-containing monomers such as monomethyl ester and itonate monomethyl ester, acid anhydride group-containing monomers such as maleic anhydride and itonic acid anhydride, glycidyl (meth)acrylate, α-ethyl glycidyl acrylate, Epoxy group-containing monomers such as 3,4-epoxybutyl (meth)acrylate, alkoxy polyalkylene glycol (meth)acrylates such as methoxypolyethylene glycol (meth)acrylate , N,N-dimethylacrylamide, hydroxyethylacrylamide, etc. (Branch component: Macromonomer) The acrylic copolymer (A1) preferably introduces a macromonomer as a branch component of the graft copolymer, and contains a repeating unit derived from the macromonomer. The so-called macromolecular monomer refers to a polymer monomer with terminal polymerizable functional groups and high molecular weight skeleton components. The glass transition temperature (Tg) of the macromonomer is preferably higher than the glass transition temperature of the copolymer component constituting the acrylic copolymer (A1). Specifically, since the glass transition temperature (Tg) of the macromonomer will affect the heating melting temperature (hot melt temperature) of the adhesive sheet, the glass transition temperature (Tg) of the macromonomer is preferably 30°C ~ 120°C, more preferably 40°C or more or 110°C or less, and more preferably 50°C or more or 100°C or less. As long as the glass transition temperature (Tg) is such, excellent processability and storage stability can be maintained by adjusting the molecular weight, and the melting temperature can be adjusted to be around 50°C to 80°C. The so-called glass transition temperature of a macromonomer refers to the glass transition temperature of the macromonomer itself, which can be measured by a differential scanning calorimeter (DSC). In addition, in order to maintain the state of physical cross-linking as an adhesive composition so that the branch components are attracted to each other at room temperature, and by heating to an appropriate temperature, the above-mentioned physical cross-linking is released and fluidity can be obtained. , it is also preferred to adjust the molecular weight or content of the macromonomer. From this point of view, the macromonomer is preferably contained in the acrylic copolymer (A1) at a ratio of 5% to 30% by mass, and more preferably 6% by mass or more or 25% by mass or less, which is more preferably Preferably, it is 8 mass % or more or 20 mass % or less. Furthermore, the number average molecular weight of the macromonomer is preferably at least 500 and less than 8,000, more preferably at least 800 and less than 7,500, and more preferably at least 1,000 but less than 7,000. As the macromonomer, any conventional manufacturer (for example, macromonomer manufactured by Toagosei Co., Ltd., etc.) can be used appropriately. The high molecular weight skeleton component of the macromonomer preferably contains an acrylic polymer or a vinyl polymer. Examples of the high molecular weight skeleton component of the macromonomer include: (methyl)acrylate, ethyl(meth)acrylate, propyl(meth)acrylate, isopropyl(meth)acrylate, n-butyl methacrylate, isobutyl (meth)acrylate, 2nd butyl (meth)acrylate, 3rd butyl (meth)acrylate, amyl (meth)acrylate, (meth)acrylic acid Isoamyl ester, neopentyl (meth)acrylate, hexyl (meth)acrylate, cyclohexyl (meth)acrylate, heptyl (meth)acrylate, 2-ethylhexyl (meth)acrylate, n-octyl acrylate, isooctyl acrylate, nonyl (meth)acrylate, isononyl (meth)acrylate, tert-butylcyclohexyl (meth)acrylate, decyl (meth)acrylate, (meth)acrylate Isodecyl acrylate, undecyl (meth)acrylate, lauryl (meth)acrylate, cetyl (meth)acrylate, stearyl (meth)acrylate, iso(meth)acrylate Stearyl ester, behenyl acrylate, isopropyl (meth)acrylate, 2-phenoxyethyl (meth)acrylate, 3,5,5-trimethylcyclohexane acrylate, p-cumylbenzene Phenol EO modified (meth)acrylate, dicyclopentyl (meth)acrylate, dicyclopentenyl (meth)acrylate, dicyclopentenoxyethyl (meth)acrylate, (meth)acrylate )Benzyl acrylate, hydroxyalkyl (meth)acrylate, (meth)acrylic acid, glycidyl (meth)acrylate, (meth)acrylamide, N,N-dimethyl(meth)acrylene (Meth)acrylate monomers such as amide, (meth)acrylonitrile, alkoxyalkyl (meth)acrylate, alkoxypolyalkylene glycol (meth)acrylate, or styrene , tertiary butyl styrene, α-methyl styrene, vinyl toluene, alkyl vinyl monomer, alkyl vinyl ester, alkyl vinyl ether, hydroxyalkyl vinyl ether and other vinyl monomers, etc. It can be used individually or in combination of 2 or more types. Examples of the terminal polymerizable functional group of the macromonomer include a methacryl group, an acryl group, a vinyl group, and the like. [Cross-linking agent (B)] The cross-linking agent (B) is preferably a cross-linking agent having at least double bond cross-linking. Examples include those selected from the group consisting of (meth)acrylyl group, epoxy group, isocyanate group, carboxyl group, hydroxyl group, carbodiimide group, oxazolinyl group, aziridinyl group, vinyl group, amine group, and imine group. A cross-linking agent containing at least one cross-linking functional group among a group and a amide group may be used alone or in combination of two or more types. Furthermore, the form in which the cross-linking agent (B) and the (meth)acrylic copolymer (A) are chemically bonded is also included. Among them, polyfunctional (meth)acrylate is preferably used. Here, polyfunctional means having two or more crosslinking functional groups. Furthermore, it may also have 3 or more or 4 or more crosslinking functional groups if necessary. Furthermore, the above-mentioned cross-linkable functional group may also be protected by a deprotectable protecting group. Examples of such polyfunctional (meth)acrylates include 1,4-butanediol di(meth)acrylate, neopentyl glycol di(meth)acrylate, and glycerol di(meth)acrylate. Ester, glyceryl glycidyl ether di(meth)acrylate, 1,6-hexanediol di(meth)acrylate, 1,9-nonanediol di(meth)acrylate, tricyclodecane dimethanol Di(meth)acrylate, bisphenol A polyethoxy di(meth)acrylate, bisphenol A polyalkoxy di(meth)acrylate, bisphenol F polyalkoxy di(meth)acrylate Acrylate, polyalkylene glycol di(meth)acrylate, trimethylolpropane trioxyethyl(meth)acrylate, ε-caprolactone modified tris(2-hydroxyethyl)iso Cyanurate tri(meth)acrylate, pentaerythritol tri(meth)acrylate, propoxylated pentaerythritol tri(meth)acrylate, ethoxylated pentaerythritol tri(meth)acrylate, pentaerythritol tetra(meth)acrylic acid Ester, propoxypentaerythritol tetra(meth)acrylate, ethoxylated pentaerythritol tetra(meth)acrylate, dipentaerythritol hexa(meth)acrylate, polyethylene glycol di(meth)acrylate, tris(acrylamide) Oxyethyl) isocyanurate, pentaerythritol tetra(meth)acrylate, dipentaerythritol hexa(meth)acrylate, dipentaerythritol penta(meth)acrylate, tripentaerythritol hexa(meth)acrylate, Tripentaerythritol penta(meth)acrylate, hydroxypivalic acid neopentyl glycol di(meth)acrylate, hydroxypivalic acid neopentyl glycol di(meth)acrylate, ε-caprolactone adduct of hydroxypivalic acid neopentyl glycol di(meth)acrylic acid There are many UV curing types such as ester, trimethylolpropane tri(meth)acrylate, alkoxylated trimethylolpropane tri(meth)acrylate, ditrimethylolpropane tetra(meth)acrylate, etc. Functional monomers include polyester (meth)acrylate, epoxy (meth)acrylate, (meth)acrylic urethane, polyether (meth)acrylate and other multifunctional acrylics. Ester oligomers, polyfunctional acrylamide, etc. can also be mentioned. Among the above examples, from the viewpoint of improving the adhesion to the adherend or the damp heat whitening inhibitory effect, the above-mentioned polyfunctional (meth)acrylate monomer preferably contains a hydroxyl group, a carboxyl group, a amide group, etc. Polyfunctional monomers or oligomers with polar functional groups. Among them, it is preferable to use a polyfunctional (meth)acrylate having a hydroxyl group or a amide group. From the viewpoint of preventing moist heat whitening, it is preferable to contain a hydrophobic acrylate monomer and a hydrophilic acrylate monomer as the dry components of the (meth)acrylate copolymer (A1), that is, the graft copolymer. , and more preferably, a polyfunctional (meth)acrylate having a hydroxyl group is used as the cross-linking agent (B). In addition, in order to adjust effects such as adhesion, moisture-heat resistance, and heat resistance, a monofunctional or polyfunctional (meth)acrylate that reacts with the cross-linking agent (B) may be further added. Regarding the content of the cross-linking agent (B), from the viewpoint of balancing the softness and cohesion of the adhesive composition, it is preferably: It is contained in a ratio of 0.1 to 20 parts by mass, and a ratio of 0.5 parts by mass or more or 15 parts by mass or less is particularly preferred, and a ratio of 1 part by mass or more or 13 parts by mass or less is particularly preferred. [Photopolymerization initiator (C)] The photopolymerization initiator (C) used in this adhesive sheet functions as a reaction initiating aid in the cross-linking reaction of the cross-linking agent (B). It is preferably By irradiating visible light, such as light in the wavelength range of 380 nm to 700 nm, free radicals are generated and become the starting point of the polymerization reaction of the base resin. However, radicals can be generated by irradiating only visible light, and radicals can also be generated by irradiating light in a wavelength range other than the visible light range. From this point of view, the absorption coefficient of the photopolymerization initiator (C) at a wavelength of 405 nm is particularly preferably 10 mL/(g∙cm) or more, particularly preferably 15 mL/(g∙cm) or more, where Particularly preferred is 25 mL/(g∙cm) or more. On the other hand, the upper limit of the absorption coefficient at a wavelength of 405 nm is preferably 1×10 4 mL/(g∙cm) or less, more preferably 1×10 3 mL/(g∙cm) or less. The absorption coefficient in the present invention is equivalent to the absorbance when the optical path length is 1 cm when the photopolymerization initiator (C) is a methanol solution with a concentration of 1 g/L. Furthermore, the absorption coefficient of the photopolymerization initiator (C) does not mean only absorbing light of a specific wavelength, but means the decomposition performance (free radical generation energy) of light of a specific wavelength. Specifically, "absorption coefficient at a wavelength of 405 nm" refers to the decomposition performance (free radical generation energy) of the photopolymerization initiator when irradiated with light of a wavelength of 405 nm. As a photopolymerization initiator with an absorption coefficient of 10 mL/(g∙cm) or more at a wavelength of 405 nm, examples include: 2-benzyl-2-dimethylamino-1-(4-morpholinyl) Phenyl)butan-1-one, 2-(4-methylbenzyl)-2-dimethylamino-1-(4-morpholinylphenyl)butan-1-one, bis(eta 5-2,4 -cyclopentadien-1-yl)-bis(2,6-difluoro-3-(1H-pyrrol-1-yl)phenyl)titanium, bis(2,4,6-tri Toluyl)-phenylphosphine oxide, 2,4,6-trimethylbenzyldiphenylphosphine oxide, (2,4,6-trimethylbenzoyl)ethoxy Phenylphosphine oxide, bis(2,6-dimethoxybenzoyl)2,4,4-trimethylpentylphosphine oxide, 9-oxosulfide𠮿 , 2-chloro-9-oxosulfide𠮿 , 3-Methyl-9-oxosulfide𠮿 , 2,4-dimethyl-9-oxosulfide𠮿 , anthraquinone, 2-methylanthraquinone, 2-ethylanthraquinone, 2-tert-butylanthraquinone, 2-aminoanthraquinone, 1,2-octanedione-1-(4-(phenylthio) base)-2-(o-benzoyl oxime)), 1-[9-ethyl-6-(2-methylbenzoyl)-9H-carbazol-3-yl]-ethanone- 1-(o-acetyl oxime), camphorquinone, and trioxime series photopolymerization initiators. In addition, the photopolymerization initiator (C) and the (meth)acrylic copolymer (A) are chemically bonded. Any one of these or derivatives thereof may be used, and two or more of these may be used in combination. In addition, it can also be used together with a photopolymerization initiator whose absorption coefficient at a wavelength of 405 nm is less than 10 mL/(g∙cm). Photopolymerization initiators are roughly classified into two types based on the free radical generation mechanism. They are roughly divided into cleavage-type photopolymerization initiators and hydrogen-absorbing photopolymerization initiators. The cleavage-type photopolymerization initiator can make photopolymerization The single bond of the initiator itself is decomposed to produce free radicals. The hydrogen-absorbing photopolymerization initiator is a photo-excited initiator that forms an excited complex with the hydrogen donor in the system to enable the hydrogen donor. of hydrogen transfer. The cleavage-type photopolymerization initiator in these decomposes into other compounds when free radicals are generated by light irradiation. Once excited, it no longer has the function of being a reaction initiator. Therefore, if the intramolecular cleavage type is used as the photopolymerization initiator (C) having an absorption wavelength in the visible light region, compared with the case of using the hydrogen-absorbing type, after the adhesive sheet is cross-linked by light irradiation, It is preferable that the light-reactive photopolymerizable initiator is less likely to remain in the adhesive composition and cause unexpected changes over time, cross-linking acceleration, and decomposition acceleration of the adhesive sheet. Furthermore, regarding the coloring unique to the photopolymerizable initiator, there was a risk of coloration when adding a photopolymerization initiator that irradiates visible light to harden the adhesive. However, the visible light region of the reaction decomposition product is Absorption disappears, it is better to choose achromatic ones appropriately. On the other hand, hydrogen-absorbing photopolymerization initiators do not produce decomposition products like cleavage-type photopolymerization initiators when they undergo free radical generation reactions by irradiation with active energy rays such as ultraviolet rays, so they are less likely to volatilize after the reaction. Ingredients can reduce damage to the adherend. Examples of the cleavage type photopolymerization initiator include: 2,2-dimethoxy-1,2-diphenylethan-1-one, 1-hydroxycyclohexylphenylketone, 2-hydroxy- 2-Methyl-1-phenyl-propan-1-one, 1-(4-(2-hydroxyethoxy)phenyl)-2-hydroxy-2-methyl-1-propan-1-one, 2-Hydroxy-1-[4-{4-(2-hydroxy-2-methyl-propanyl)benzyl}phenyl]-2-methyl-propan-1-one, oligo(2-hydroxy -2-Methyl-1-(4-(1-methylvinyl)phenyl)acetone), methyl phenylglyoxylate, 2-benzyl-2-dimethylamino-1-(4 -Morpholinylphenyl)butan-1-one, 2-methyl-1-[4-(methylthio)phenyl]-2-morpholinylpropan-1-one, 2-(dimethyl Amino)-2-[(4-methylphenyl)methyl]-1-[4-(4-morpholinyl)phenyl]-1-butanone, bis(2,4,6-trimethyl ((2,4,6-Trimethylbenzoyl)-phenylphosphine oxide, 2,4,6-trimethylbenzyldiphenylphosphine oxide, (2,4,6-trimethylbenzoyl)ethoxybenzene phosphine oxide, bis(2,6-dimethoxybenzoyl)2,4,4-trimethylpentylphosphine oxide, or their derivatives, etc. Among them, bis(2,4,6-trimethylbenzoyl)-phenylphosphine oxide is preferred in terms of using a cleavage-type photopolymerizable initiator and converting it into a decomposed product after the reaction and decolorizing it. , 2,4,6-trimethylbenzoyldiphenylphosphine oxide, (2,4,6-trimethylbenzoyl)ethoxyphenylphosphine oxide, bis(2,6-di Methoxybenzoyl)-2,4,4-trimethylpentylphosphine oxide and other acylphosphine oxide photoinitiators. Furthermore, in terms of compatibility with an acrylic copolymer including a graft copolymer having a macromonomer as a branch component, it is preferable to use 2,4,6-trimethylbenzoyldiphenyl oxidation. Phosphine, (2,4,6-trimethylbenzoyl)ethoxyphenylphosphine oxide, bis(2,6-dimethoxybenzoyl)-2,4,4-trimethyl Pentylphosphine oxide or the like serves as the photopolymerization initiator (C). The content of the photopolymerization initiator (C) is not particularly limited. For example, based on 100 parts by mass of the (meth)acrylic copolymer (A), it is preferably contained at a ratio of 0.1 to 10 parts by mass, and particularly preferably at a ratio of 0.2 parts by mass or more or 5 parts by mass or less. Particularly preferably, it is contained in a ratio of 0.5 parts by mass or more or 3 parts by mass or less. However, in terms of balance with other factors, it can also exceed this range. The photopolymerization initiator can be used alone or in combination of two or more types. [Ultraviolet absorber (D)] The ultraviolet absorber (D) only needs to be a substance that can absorb ultraviolet rays. As a standard, it is preferable that the wavelength of the transparent double-sided adhesive sheet can be changed by adding the ultraviolet absorber (D). Substances whose absorbance at 380 nm is above 0.3 mL/(g∙cm), especially above 0.5 mL/(g∙cm), especially above 1.0 mL/(g∙cm). In addition, the absorbance at a wavelength of 380 nm is calculated according to the following formula. A 380 =-Log(T 380 /100) A 380 : Absorbance T 380 at a wavelength of 380 nm; Transmittance (%) at 380 nm of a transparent double-sided adhesive sheet. As the ultraviolet absorber (D), for example, preferably Having one selected from the group consisting of benzotriazole structure, benzophenone structure, trisulfonate structure, benzoate structure, oxalaniline structure, salicylate structure and cyanoacrylate structure, or Two or more structures. Among them, from the viewpoint of ultraviolet absorbability, those having one or more structures selected from the group consisting of benzotriazole structure, trisulfonate structure and benzophenone structure are preferred. Furthermore, from the viewpoint of compatibility with an acrylic copolymer including a graft copolymer having a macromer as a branch component, it is preferable to use a benzotriazole structure or a benzophenone structure as the ultraviolet absorber. Agent (D). The content of the ultraviolet absorber (D) is not particularly limited. For example, based on 100 parts by mass of the (meth)acrylic copolymer (A), it is preferably contained at a ratio of 0.01 to 10 parts by mass, and particularly preferably at a ratio of 0.1 parts by mass or more or 5 parts by mass or less. Particularly preferably, it is contained in a ratio of 0.2 parts by mass or more or 3 parts by mass or less. However, in terms of balance with other factors, it can also exceed this range. From the viewpoint of absorbing ultraviolet rays and initiating photopolymerization in the visible light range other than the ultraviolet rays, the ratio of the ultraviolet absorber (D) to 100 parts by mass of the photopolymerization initiator (C) is preferably 25 to 400 parts by mass. , particularly preferably at least 50 parts by mass or less than 300 parts by mass, and particularly preferably at least 80 parts by mass or less than 250 parts by mass. The ultraviolet absorber may be used alone or in combination of two or more types. [Other Ingredients] This adhesive sheet may also contain known ingredients prepared in ordinary adhesive compositions as ingredients other than the above. For example, an adhesion-imparting resin, antioxidant, light stabilizer, metal deactivator, anti-rust agent, anti-aging agent, hygroscopic agent, water-repellent agent, sensitizer, antistatic agent, defoaming agent, etc. may be appropriately contained. Various additives such as inorganic particles. Moreover, if necessary, a reaction catalyst (a tertiary amine compound, a quaternary ammonium compound, a tin laurate compound, etc.) may be appropriately contained as needed. [Preferred Composition Example] As an example of a particularly preferable composition of the present adhesive composition, the following composition example can be cited, that is, an acrylic copolymer containing a graft copolymer having a macromonomer as a branch component as (form (B) acrylic copolymer (A), containing a difunctional, trifunctional, or other polyfunctional (meth)acrylate compound as a cross-linking agent (B), and a cleavage-type photopolymerization initiator as a photopolymerization initiator (C) ), and contains an ultraviolet absorber having a benzotriazole structure or a benzophenone structure as the ultraviolet absorber (D). However, it is not limited to this composition. [Laminated structure] The adhesive sheet may be a sheet composed of a single layer or a multi-layer sheet composed of two or more layers laminated. When this adhesive sheet is made into a multi-layered adhesive sheet, that is, when it forms an adhesive sheet having a laminated structure of an intermediate layer and an outermost layer, it is preferable that the outermost layer is formed of this adhesive composition. When the present adhesive sheet has a multi-layer structure, the ratio of the thickness of each outermost layer to the thickness of the middle layer is preferably 1:1 to 1:20, and more preferably 1:2 to 1:10. If the thickness of the intermediate layer is within the above range, it is preferable because the influence of the thickness of the adhesive material layer in the laminated body will not be too great and the workability of cutting or operation will not be deteriorated due to being too soft. Furthermore, when the outermost layer is in the above range, it is preferable because there is no problem in poor followability to uneven or curved surfaces and the adhesion or wettability to the adherend can be maintained. An example of the case where the present adhesive sheet has a multilayer structure is a multilayer structure including an intermediate layer (α layer) and a surface layer (β layer). The intermediate layer (α layer) contains the present adhesive composition, that is, contains ( Meth)acrylic copolymer (A), cross-linking agent (B), photopolymerization initiator (C) with an absorption coefficient of 10 mL/(g∙cm) or more at a wavelength of 405 nm, and ultraviolet absorber (D) ) adhesive resin composition, the surface layer (β layer) contains (meth)acrylic copolymer (A) and cross-linking agent (B), and does not contain ultraviolet absorber (D). Specific laminate structures include β layer/α layer/β layer, β layer/α layer/β layer/α layer/β layer, and the like. Among them, two types of three layers, β layer/α layer/β layer, are more preferred. Other layers, represented by outgassing barrier layers, may also be interposed between the α layer and the β layer as necessary. By providing a surface layer (β layer) containing the (meth)acrylic copolymer (A) and the cross-linking agent (B) and not containing the ultraviolet absorber (D), the ultraviolet absorber (D) in the α layer can be suppressed. Oozing. Furthermore, when the resin composition forming the β layer contains the photopolymerization initiator (C), its decomposition product, or the ultraviolet absorber (D), for example, the α layer (intermediate layer) and the β layer When the (surface layers) are overlapped and irradiated with light, the β layer as the surface layer may absorb light and intercept the light reaching the α layer as the intermediate layer, or the ultraviolet absorber (D) may transfer from the β layer to the α layer and block the α layer. The risk of light hardening. From the above viewpoint, the β layer preferably does not have photocurability, and more preferably has thermosetting property. Among them, the β layer is more preferably a resin composition containing no photopolymerization initiator (C) and ultraviolet absorber (D). In the multilayer structure including the above-mentioned α layer and β layer, the cross-linking agent (B) used in the α layer is preferably one containing hydroxyl or Polyfunctional monomers or oligomers with polar functional groups such as carboxyl groups. Among them, it is more preferable to use a polyfunctional (meth)acrylic monomer having a hydroxyl group. The content of the cross-linking agent (B) in the α layer is preferably 0.5 to 50 parts by mass relative to 100 parts by mass of the acrylic copolymer (A) in the α layer, and preferably 1 part by mass or more or 40 parts by mass. Among the following ratios, a ratio of 5 parts by mass or more or 30 parts by mass or less is preferred. By containing the cross-linking agent (B) in this range, the curing reaction fully proceeds in a short time, so it is easy to balance the reliability after curing with the moisture and heat whitening resistance, flexibility, processability when molded into a sheet, etc. . On the other hand, the cross-linking agent (B) used in the β layer preferably contains one selected from the group consisting of (meth)acryl group, epoxy group, isocyanate group, melamine group, and glycol group from the viewpoint of thermosetting properties. A cross-linking agent with at least one organic functional group among group, siloxane group and amine group. The content of the cross-linking agent (B) in the β layer is preferably 0.1 to 20 parts by mass relative to 100 parts by mass of the acrylic copolymer (A) in the β layer, and preferably 0.2 parts by mass or more or 10 parts by mass. ratio below. By containing the cross-linking agent (B) in this range, the curing reaction fully proceeds in a short time, so after curing, as an adhesive sheet, it is easy to improve the stickiness, reliability, foaming resistance, and step absorption (foreign matter) Grindability), softness, and processability when formed into sheets are balanced. Furthermore, it is more preferable to add more cross-linking agent (B) to the α layer than to the β layer. By imparting high elasticity to the hardened α layer and allowing it to function as a core material, the adhesive sheet can be provided with excellent operability. In the multilayer structure including the above-mentioned α layer and β layer, from the viewpoint that the α layer absorbs ultraviolet rays and starts photopolymerization in the visible light region other than the ultraviolet rays, in the α layer, relative to the photopolymerization initiator ( C) 100 parts by mass, the ultraviolet absorber (D) preferably contains 25 to 400 parts by mass, more preferably 50 parts by mass or more or 300 parts by mass or less, and further preferably 80 parts by mass or more or 250 parts by mass or less. In the multilayer structure including the above-mentioned α layer and β layer, the order of laminating the α layer and the β layer and the order of hardening are not particularly limited. Specifically, the following lamination method can be exemplified. Method I: After laminating unhardened α layer and β layer, the α layer and β layer are hardened by light irradiation or heat. Method II: A method in which a β layer hardened by heat or the like is laminated on an unhardened α layer, and then the α layer is hardened by light irradiation. Method III: A method in which an unhardened β layer is laminated on an α layer hardened by light irradiation, and then the β layer is hardened by heat or the like. Method IV: A method of overlapping the α layer and β layer that are formed and hardened separately. Among them, method II is more preferable in terms of strong inter-layer adhesion, excellent resistance to wet and heat foaming, reliability, and ability to inhibit the bleed-out of ultraviolet absorbers. The β layer is preferably thermally hardened. The heating temperature for hardening the β layer is not particularly limited and can be appropriately adjusted depending on the type and amount of the cross-linking agent (B) contained in the β layer. Taking into account the workability of the resin composition before curing or the heat resistance of the resin, specifically, 40 to 200°C is preferred, 50°C or higher or 180°C or lower is more preferred, and 60°C is even more preferred. Above or below 150℃. On the other hand, the α layer is preferably photocured. The amount of light irradiation used to harden the α layer is preferably 100 to 8000 mJ/cm 2 based on a wavelength of 405 nm, more preferably 500 mJ/cm 2 or more or 5000 mJ/cm 2 or less, and further more preferably More than 1000 mJ/ cm2 or less than 4000 mJ/ cm2 . Examples of light sources for emitted light include high-pressure mercury lamps, metal halide lamps, and LED lamps. At this time, the adhesive sheet can also be irradiated with light that does not substantially contain light with wavelengths below 380 nm, preferably visible light, to cause the adhesive sheet to be photo-crosslinked. The so-called "light that does not substantially contain light with wavelengths less than 380 nm" refers to light with a transmittance of less than 10% for light with wavelengths less than 380 nm. As a method of irradiating visible light with wavelengths that do not include the ultraviolet range, a light source that emits only visible light with wavelengths that do not include the ultraviolet range can be used, or a filter that does not transmit light with wavelengths that does not include the ultraviolet range can be used. Film irradiation. In the multilayer structure including the above α layer and β layer, the thickness of the α layer is preferably 10 to 400 μm, more preferably 20 μm or more or 300 μm or less, and still more preferably 30 μm or more or 200 μm or less. The thickness of the β layer is preferably 1 to 60 μm, more preferably 3 μm or more or 40 μm or less, and still more preferably 5 μm or more or 25 μm or less. The ratio of the thickness of the α layer to the thickness of the β layer is preferably 1:1 to 1:20, and more preferably 1:2 to 1:15. If the thickness of the α layer (intermediate layer) is within the above range, ultraviolet absorbing properties can be easily obtained, and the photocurable properties of the α layer can be easily achieved. In addition, it is preferable because it does not deteriorate the workability of cutting or handling due to excessive softness. If the thickness of the β layer (surface layer) is within the above range, it is preferable because there is no problem in poor followability to uneven or curved surfaces and the adhesion or wettability to the adherend can be maintained. [Sheet Thickness] Regarding the thickness of this adhesive sheet, by making the sheet thickness thinner, it can respond to the thinning requirements. On the other hand, if the sheet thickness is too thin, for example, the surface to be adhered may have uneven portions. In this case, it may not be able to fully follow the concave and convex, or it may not be able to exert sufficient adhesion. From this point of view, the thickness of the adhesive sheet is preferably 20 to 500 μm, particularly preferably 25 μm or more or 350 μm or less, and particularly preferably 50 μm or more or 250 μm or less. [Characteristics] The ultraviolet transmittance (JIS K7361-1) of this adhesive sheet is preferably 50% or less at a wavelength of 380 nm, more preferably 30% or less, and more preferably 10% or less. On the other hand, the light transmittance at a wavelength of 420 nm, which is a visible light region, is preferably 70% or more, more preferably 80% or more, and further preferably 85% or more. The viscosity of the transparent double-sided adhesive sheet of the present invention at 100°C is preferably 50 Pa∙s to 5000 Pa∙s, more preferably 100 Pa∙s or more or 3000 Pa∙s or less, especially 150 Pa∙s. s or above or below 2500 Pa∙s. <Adhesive sheet laminate> This adhesive sheet can be used alone. In addition, it can also be used by laminating it with other members. (The present adhesive sheet laminate) For example, a film, such as a release film or a protective film, or a film thereof may be laminated on one or both sides of the present adhesive sheet to form an adhesive sheet laminate (referred to as "the present adhesive sheet"). Adhesive sheet laminate"). An example is the following case: In this adhesive sheet laminate, the release film on one or both sides is a release film with a light transmittance of 40% or less for light with a wavelength of 410 nm or less. The reason is that if the transmittance of at least one release film for light with a wavelength of 410 nm or less is 40% or less, by laminating the release film on the adhesive sheet, even if the adhesive sheet contains light with a wavelength of 405 nm, Photopolymerization initiator (C) with an absorbance coefficient of 10 mL/(g∙cm) or above can also effectively prevent photopolymerization from being promoted due to irradiation of visible light. From this point of view, the light transmittance of one or two release films for light having a wavelength of 410 nm or less is preferably 40% or less, more preferably 30% or less, and still more preferably 20% or less. Here, as a release film having a light transmittance of 40% or less for light with a wavelength of 410 nm or less, that is, a release film that has the function of partially blocking the transmitted light of visible light and ultraviolet light, examples include: The cast film or stretched film of polyester, polypropylene or polyethylene resin with ultraviolet absorber is coated with polysiloxane resin and then subjected to mold release treatment. Examples include multilayer cast films in which a layer containing a resin containing no UV absorber is formed on one or both sides of a layer containing a polyester, polypropylene, or polyethylene resin blended with an UV absorber. Or one side of the stretched film is coated with polysiloxane resin and then released. Another example is to apply a coating containing an ultraviolet absorber to one side of a cast film or stretched film containing a polyester, polypropylene, or polyethylene resin to form an ultraviolet absorbing layer, and then apply a polyethylene coating on the ultraviolet absorbing layer. Those who perform release treatment using silicone resin. Alternatively, one side of a cast film or stretched film containing a polyester, polypropylene, or polyethylene resin may be coated with a coating containing an ultraviolet absorber to form an ultraviolet absorbing layer, and the other side may be coated with a polysiloxane resin. The person who performs the demoulding process. Alternatively, the other side of a resin film containing a polyester, polypropylene, or polyethylene resin that has been subjected to a release treatment and a separately prepared resin film that has not been subjected to a release treatment is passed through an adhesive layer containing an ultraviolet absorber. Or it is formed by laminating adhesive layers. The above-mentioned release film may also have an antistatic layer or other layers such as a hard coating layer and an adhesion-promoting layer as needed. If the thickness of the release film is too thick, the cutting processability will be poor, and if it is too thin, the workability will be poor, and there is a possibility of dents easily forming on the adhesive sheet. From this viewpoint, the thickness of the release film is preferably 20 μm or more and 300 μm or less, particularly preferably 25 μm or more or 250 μm or less, and particularly preferably 38 μm or more or 200 μm or less. In the case where a release film is laminated on both sides, it is preferable to make the thickness or peeling force of one release film and the other release film different. In addition, an example can be given in which the film on one or both sides of the present adhesive sheet laminate is a film with a light transmittance of 40% or less for light with a wavelength of 380 nm or more and 410 nm or less, such as a release film or a protective film. film or a film formed by laminating these. That is, a photopolymerization initiator (C) containing a (meth)acrylic copolymer (A), a cross-linking agent (B), and an absorption coefficient at a wavelength of 405 nm of 10 mL/(g∙cm) or more The transparent double-sided adhesive sheet of the adhesive resin composition containing the ultraviolet absorber (D) is laminated on one or both sides with a film having a transmittance of 40% or less for light with a wavelength of 380 nm or more and 410 nm or less. It can inhibit at least a wavelength of 405 nm from being exposed to the transparent double-sided adhesive sheet, thus inhibiting the generation of free radicals from the photopolymerization initiator (C). From this point of view, it is further preferred that the film on one side or both sides of the adhesive sheet laminate has a light transmittance of 40% or less for light with a wavelength of 380 nm or more and 410 nm or less, and more preferably 30%. below, preferably 20% or less, and still more preferably 10% or less. Furthermore, as a preferred example of the structure, a surface protective film having a transmittance of 40% or less for light having a wavelength of 410 nm or less is layered on one surface or both surfaces of the adhesive sheet laminate. The reason for this is that at least one area of the adhesive sheet laminate is coated with a surface protective film having a transmittance of 40% or less for light with a wavelength of 410 nm or less. Therefore, even if the adhesive sheet contains a light absorption coefficient of 10 at a wavelength of 405 nm, The photopolymerization initiator (C) with an amount of mL/(g∙cm) or above can also effectively prevent the advancement of photopolymerization due to irradiation of visible light. From this point of view, the surface protective film laminated on one or both sides of the adhesive sheet laminate preferably has a light transmittance of 40% or less for light with a wavelength of 410 nm or less, more preferably 30% or less, and more preferably 30% or less. Preferably it is 20% or less. Here, as a surface protective film having a light transmittance of 40% or less for light with a wavelength of 410 nm or less, that is, a surface protective film that has the function of blocking part of the transmitted light of visible light and ultraviolet light, for example, polyester can be used A laminated film that is a polypropylene-based, polyethylene-based cast film or stretched film coated with a re-peelable micro-adhesive resin on one side, and has an ultraviolet absorbing layer coated with a paint containing an ultraviolet absorber on the other side. Also, examples include those in which a re-peelable slightly adhesive resin mixed with an ultraviolet absorber is coated on one side of a polypropylene-based or polyethylene-based cast film or stretched film. Also, examples include cast films or stretched films containing polyester-based, polypropylene-based, or polyethylene-based resins blended with ultraviolet absorbers, and coated with a releasable microadhesive resin. Examples include multilayer cast films in which a layer containing a resin containing no UV absorber is formed on one or both sides of a layer containing a polyester, polypropylene, or polyethylene resin blended with an UV absorber. Or one side of the stretch film is coated with a re-peelable slightly adhesive resin. Another example is to apply a coating containing an ultraviolet absorber to one side of a cast film or stretched film containing a polyester, polypropylene, or polyethylene resin to form an ultraviolet absorbing layer, and then coat the ultraviolet absorbing layer with an ultraviolet absorbing layer. Re-peelable slightly adhesive resin. Alternatively, one side of a cast film or stretched film containing polyester, polypropylene, or polyethylene resin may be coated with a coating containing an ultraviolet absorber to form an ultraviolet absorbing layer, and the other side may be coated with a re-peelable coating. Slightly sticky resin. Alternatively, a resin film containing a polyester-based, polypropylene-based, or polyethylene-based resin coated with a releasable microadhesive resin on one side and a separately prepared resin film can be passed through a resin film containing an ultraviolet absorber on the other side. It is formed by laminating subsequent layers or adhesive layers. The above-mentioned surface protective film may also have an antistatic layer, a hard coating layer, an adhesion-promoting layer and other layers as needed. (Laminated body for constituting the image display device) In addition, two constituent members for the image display device can be laminated via this adhesive sheet to form a laminate for constituting the image display device (referred to as "the present image display device"). "Structured laminate"). In this case, as the two components for the image display device, for example, any one of the group consisting of a touch sensor, an image display panel, a surface protection panel, and a polarizing film, or a combination of two or more . Specific examples of the laminated body for constituting the image display device include the following structures: release sheet/this adhesive sheet/touch panel, release sheet/this adhesive sheet/protective panel, release sheet/ This adhesive sheet/image display panel, image display panel/this adhesive sheet/touch panel, image display panel/this adhesive sheet/protective panel, image display panel/this adhesive sheet/touch panel/this adhesive sheet /Protective panel, polarizing film/this adhesive sheet/touch panel, polarizing film/this adhesive sheet/touch panel/this adhesive sheet/protective panel, etc. However, it is not limited to these lamination examples. The above-mentioned touch panel also includes a structure in which the touch panel function is built into the protective panel, or a structure in which the touch panel function is built into the image display panel. In the present image display device constituting laminate, at least one of the two image display device constituting members may have ultraviolet absorbing properties, for example, may contain an ultraviolet absorber. Since this adhesive sheet is not cured by ultraviolet light but by visible light, even if the component of the image display device has ultraviolet absorbing properties, it can be cured by irradiating visible light through the component of the image display device. Let the adhesive sheet harden. (The present image display device) An image display device (referred to as "the present image display device") can be constructed using the present adhesive sheet or the present image display device constituting laminate as described above. As the image display device, for example, an image display device such as a liquid crystal display, an organic EL display, an inorganic EL display, an electronic paper, a plasma display, or a microelectromechanical system (MEMS) display can be constructed. In the present image display device, at least one of the image display device components constituting the image display device may have ultraviolet absorbing properties, for example, may contain an ultraviolet absorber. Since this adhesive sheet is not cured by ultraviolet light but by visible light, even if the component of the image display device has ultraviolet absorbing properties, it can be cured by irradiating visible light through the component of the image display device. Let the adhesive sheet harden. ＜Characteristics and usage of this adhesive sheet＞ This adhesive sheet has ultraviolet absorption function and hardening property by being irradiated with light of wavelengths other than the ultraviolet range, especially visible light. Utilizing the characteristics of this adhesive sheet, a laminate for forming an image display device can be produced as follows, for example. After the adhesive composition is formed into a sheet (sheet production step), two image display device components are laminated through the adhesive sheet before light curing (one attachment step), and then irradiated with at least one wavelength Light of 405 nm, for example, light containing wavelengths in the visible light range, photo-crosslinks and hardens the adhesive sheet described above (secondary attachment step), whereby a laminate for forming an image display device can be produced. The light containing the wavelength of the visible light region may also include the ultraviolet region, that is, the light of the wavelength below 380 nm. However, when the components of the laminated image display device are components that are easily degraded by ultraviolet rays, it is preferable to irradiate the substance. The adhesive sheet does not contain light with a wavelength below 380 nm, that is, visible light, so that the adhesive sheet is photo-crosslinked and hardened (secondary attachment step). (Sheet production step) This adhesive composition can be formed into a sheet shape to produce this adhesive sheet. As a method of molding the present adhesive resin composition into a sheet, any conventionally known method can be used. At this time, as mentioned above, the adhesive resin composition may be formed into a sheet on the release film to produce the adhesive sheet. Alternatively, the adhesive resin composition may be formed into a sheet-like film on a component of an image display device, and the adhesive sheet may be laminated on the component of the image display device. (One-time attachment step) As long as the adhesive sheet has self-adhesiveness (stickiness), two image display device components can be attached at one time by overlapping the adhesive sheet. For example, as long as this adhesive sheet uses an acrylic copolymer (A1) containing a graft copolymer having a macromonomer as a branch component as a base polymer, it can maintain its sheet shape at room temperature and exhibit self-adhesiveness. properties, and in the uncross-linked state, under normal conditions, that is, near room temperature, it can have moderate adhesion, such as adhesion to the extent that it can be peeled off (called "stickiness"), so it can be easily attached. positioning, etc. Furthermore, when heated in an uncrosslinked state, it melts or flows (hot meltability), so the adhesive can be filled following uneven portions such as printing steps, and filling can be performed without generating bubbles. As the laminating device used during lamination, a known device can be used. Examples include: an electric heating press equipped with a heating plate, a film laminating machine, a roller laminating machine, a vacuum laminating machine, a hand pressure roller, etc. Furthermore, when the present adhesive sheet uses an acrylic copolymer (A1) containing a graft copolymer having a macromer as a branch component as a base polymer, it can provide excellent performance in a normal state, that is, in a room temperature state. Storage stability or cutting processability. In addition, due to its self-adhesiveness (stickiness), the adhesiveness of the adhesion level can be easily obtained by simply pressing this adhesive sheet against the adherend. Therefore, the positioning of the adhesive material to be adhered is easy, and the operation is very convenient. . Furthermore, since it has excellent shape retention, it can be processed into any shape in advance. Therefore, the adhesive sheet formed on the release film can be cut in advance according to the size of the components of the image display device to be laminated. The cutting method at this time is generally punching with a Thomson knife, cutting with a super cutting machine or laser. It is better to frame the release film on the front and back in a way that can easily peel off the release film. The shape remains and is cut in half. When the adhesive sheet has hot-melt properties, that is, has the property of being softened or fluidized by heating, it is preferable to heat the adhesive sheet and laminate two components of the image display device. By heating this adhesive sheet to soften or fluidize it, even if the surface to be adhered has unevenness, the adhesive sheet can be heated to follow the unevenness and fill the unevenness without gaps. As the heating mechanism of the adhesive sheet, for example, various constant temperature baths, heating plates, electromagnetic heating devices, heating rollers, etc. can be used. In order to perform lamination and heating more efficiently, for example, it is preferable to use an electric heating press, a film-type laminating machine, a roller laminating machine, etc. At this time, the adhesive sheet can also be heated by heating one or both of the components of the image display device. At this time, if the softening temperature of the adhesive sheet is 50°C or higher, processing characteristics and storage characteristics at normal temperature can be improved. On the other hand, if the softening temperature of the adhesive sheet is 100°C or lower, not only can thermal damage to the image display panel or the front panel be suppressed, but the adhesive sheet can also be prevented from overflowing due to excessive flow. Therefore, the softening temperature of this adhesive sheet is preferably 50 to 100°C, more preferably 55°C or more or 95°C or less, and particularly preferably 60°C or more or 90°C or less. When heating this adhesive sheet, it is preferable to overlay and laminate two image display device components via this adhesive sheet, and then heat the laminated body in a reduced pressure environment. By heating the laminate in a reduced pressure environment, it is possible to prevent air bubbles or foreign matter from being mixed into the adhesive sheet after lamination. (Second attachment step) In the secondary attachment step, for a laminate in which two image display device constituent members are laminated via this adhesive sheet, a layer of the image display device constituent member is passed through the laminate from the outside of at least one image display device constituent member. The member constituting an image display device irradiates the adhesive sheet with light having a wavelength of at least 405 nm, for example, light containing a wavelength in the visible light region, that is, visible light, so that the adhesive sheet is photo-crosslinked and hardened. Through such photo-crosslinking, the adhesive sheet can be fully cross-linked, so that it can have the adhesive force and cohesion to resist the outgassing air pressure generated by components of image display devices such as self-protection panels as much as possible. Furthermore, since the adhesive sheet has ultraviolet absorbing properties, it is possible to suppress deterioration of the adhesive sheet itself and the components of the image display device due to ultraviolet rays. Light with a wavelength of at least 405 nm can be irradiated from a light source including at least one or a combination of two or more selected from the group consisting of the sun, fluorescent lamps, LEDs, organic EL, inorganic EL and light-emitting modules for image display devices. When irradiating visible light, it is preferable to irradiate visible light having a wavelength that does not substantially include ultraviolet range, for example, light having a wavelength less than 365 nm. Here, the term "substantially does not contain light with wavelengths less than 365 nm" means that the luminous intensity of light with wavelengths less than 365 nm does not reach 1 mW/cm 2 . Among them, it is preferable to irradiate light with a wavelength of at least 405 nm, for example, light with a wavelength in the visible light region and substantially not containing light with a wavelength below 380 nm, to the adhesive sheet, so that the adhesive sheet is photo-crosslinked. And harden. Here, "substantially does not contain light with a wavelength of 380 nm or less" means that the luminous intensity of light with a wavelength of 380 nm or less is 5 mW/cm 2 or less, preferably 1 mW/cm 2 or less. As a method of irradiating visible rays excluding light with wavelengths below 380 nm, that is, light with wavelengths in the ultraviolet range, a light source that emits only visible rays excluding light with wavelengths excluding ultraviolet ranges can also be used. For example, a light source including at least one or a combination of two or more selected from the group consisting of the sun, fluorescent lamps, LEDs, organic EL, inorganic EL, and light-emitting modules for image display devices can be used. In addition, irradiation can also be performed through a filter that does not transmit light of wavelengths in the ultraviolet range. For example, the following method can be cited: using a high-pressure mercury lamp, a metal halide lamp, a xenon arc lamp, a carbon arc lamp and other luminous lamps that also emit light of a wavelength in the ultraviolet range, or sunlight as the light source, and transmitting light at a wavelength of 380 nm A filter with a light transmittance of less than 10% and a transmittance of more than 60% at a wavelength of 405 nm is used to irradiate visible light to the adhesive composition. The above-mentioned optical filter may be a release film constituting the present adhesive sheet laminate, or a surface protective film laminated on the surface of the present adhesive sheet laminate. When adjusting the degree of visible light cross-linking, in addition to controlling the amount of visible light irradiation, the degree of visible light cross-linking can also be adjusted by irradiating visible light through the above-mentioned filter to block part of the visible light transmission. . ＜Explanation of statements, etc.＞ In general, the so-called "sheet" refers to a thin, flat product whose thickness is small compared to the length and width according to the definition of JIS. Generally speaking, the so-called "film" ” refers to a thin and flat product whose thickness is extremely small compared to the length and width, and the maximum thickness is arbitrarily limited. It is usually supplied in the form of a roll (Japanese Industrial Standard JIS K6900). However, the boundary between the sheet and the film is not limited. In the present invention, there is no need to distinguish between the two in terms of language. Therefore, in the present invention, when it is called "film", it also includes "sheet". In the case of "sheet", "film" is also included. In addition, when expressed as a "panel" such as an image display panel, a protective panel, etc., it includes a board, a sheet, and a film. In this specification, when it is described as "X～Y" (X and Y are arbitrary numbers), unless otherwise specified, it includes the meaning of "more than X and less than Y", and also includes "preferably greater than X" or "preferably less than Y" means. In addition, when it is described as "more than X" (X is an arbitrary number), unless otherwise specified, it includes the meaning of "preferably greater than In this case, unless otherwise specified, it also includes the meaning of "preferably less than Y". [Examples] Hereinafter, examples and comparative examples will be further described. However, the present invention is not limited to these. The cumulative light quantity of light at wavelength 405 nm and wavelength 365 nm measured in this example was measured using a cumulative light quantity meter (UIT-250, manufactured by Ushio Electric Co., Ltd.). [Example 1-1] A (meth)acrylic copolymer (A) containing 15 parts by mass of polymethyl methacrylate macromonomer (Tg80°C) with a number average molecular weight of 3000 and 81 parts by mass of butyl acrylate 1 kg of copolymer (A-1, mass average molecular weight 300,000) and 4 parts by mass of acrylic acid, and glyceryl dimethacrylate (manufactured by NOF, Blemmer GMR) (B) was added as a cross-linking agent (B) -1) 100 g, 15 g of Esacure KTO46 (C-1) (manufactured by Lanberti Co., Ltd.) as the photopolymerization initiator (C), 2,6-diphenyl-4-(2) as the ultraviolet absorber (D) -Hydroxy-4-hexyloxyphenyl)-1,3,5-tris(D-1) (manufactured by BASF, TINUVIN 1577) 5 g, and mixed uniformly to obtain adhesive composition 1. The absorption coefficient of the photopolymerization initiator (C-1) at 405 nm is 7.4×10 1 (mL/(g∙cm)). Next, the above-mentioned adhesive composition 1 is formed into a sheet on a peel-treated polyethylene terephthalate film (DIAFOIL MRV, manufactured by Mitsubishi Plastics Corporation, thickness 100 μm) so that the thickness becomes 100 μm. The adhesive sheet laminate 1 was produced by covering it with a peel-processed polyethylene terephthalate film (DIAFOIL MRQ, manufactured by Mitsubishi Plastics Corporation, thickness 75 μm). [Example 1-2] 10 parts by mass of a polymethyl methacrylate macromonomer (Tg 55° C.) having a number average molecular weight of 1,400 as the (meth)acrylic copolymer (A) and 2 (meth)acrylic acid - 1 kg of acrylic graft copolymer (A-2) (weight average molecular weight: 230,000) obtained by randomly copolymerizing 90 parts by mass of ethylhexyl (Tg: -70°C) as a cross-linking agent (B ) tricyclodecane dimethacrylate (manufactured by Shin-Nakamura Chemical Co., Ltd., product name: DCP) (B-2) 50 g, as photopolymerization initiator (C) Irgacure 369 (C-2) (BASF company) 15 g, and 2-(2H-benzotriazol-2-yl)-4,6-di-tertiary amylphenol (manufactured by Johoku Chemical Co., Ltd., JF-80) as the ultraviolet absorber (D) (D-2) 20 g was uniformly mixed to prepare adhesive resin composition 2. Next, the adhesive composition 4 was applied on a peel-treated polyethylene terephthalate film (DIAFOIL MRV, manufactured by Mitsubishi Plastics Corporation, thickness 100 μm) to become 100 μm, and then the coating was peeled off. A polyethylene terephthalate film (DIAFOIL MRQ, manufactured by Mitsubishi Plastics Corporation, thickness 75 μm) was used to prepare an adhesive sheet laminate 2. The absorption coefficient of the photopolymerization initiator (C-2) at 405 nm is 1.6×10 2 (mL/(g∙cm)). [Example 1-3] Copolymerization of (meth)acrylic copolymer (A) containing 76 parts by mass of 2-ethylhexyl (meth)acrylate, 20 parts by mass of vinyl acetate, and 4 parts by mass of acrylic acid 1 kg of material (A-3, mass average molecular weight 400,000), and 200 g of pentaerythritol tetraacrylate propoxide (manufactured by Shin-Nakamura Chemical Co., Ltd., ATM-4P) (B-3) as cross-linking agent (B), as 7 g of Irgacure 819 (C-3) (manufactured by BASF) as the photopolymerization initiator (C), and 2,2'-dihydroxy-4-methoxybenzophenone as the ultraviolet absorber (D) (Kemisorb 111 manufactured by Chemipro Kasei Co., Ltd.) (D-3) 10 g and mixed uniformly to obtain adhesive composition 3. The absorption coefficient of the photopolymerization initiator (C-3) at 405 nm is 9.0×10 2 (mL/(g∙cm)). The adhesive resin composition 3 was sandwiched between two peel-processed polyethylene terephthalate films (DIAFOIL MRF manufactured by Mitsubishi Plastics Corporation, thickness 75 μm/DIAFOIL MRT manufactured by Mitsubishi Plastics Corporation, thickness 38 μm), and It was shaped into a sheet so that the thickness became 100 μm, and a sheet (α) for an intermediate layer was produced. To 1 kg of a commercially available adhesive solution containing an acrylic copolymer (A-4, mass average molecular weight 1.3 million) (manufactured by Soken Chemical Co., Ltd., SK-Dyne 1882, solid content concentration approximately 17%), an isocyanate-based crosslinker was added. 1.85 g of L-45 (B-5) (manufactured by Soken Chemical Co., Ltd.) as a linking agent and 0.5 g of E-5XM (B-6) (manufactured by Soken Chemical Co., Ltd.) as an epoxy cross-linking agent were used to prepare an adhesive composition. 4. On the peeled polyethylene terephthalate film (DIAFOIL MRV manufactured by Mitsubishi Plastics Corporation, thickness 100 μm), apply the above-mentioned adhesive layer coating so that the film thickness after drying becomes 20 to 30 μm. After applying the liquid, dry at 80°C for 5 minutes. This was cured at 23°C for 7 days to allow the cross-linking agent to react, thereby producing an adhesive layer sheet (β). Furthermore, on the peeled polyethylene terephthalate film (made by Mitsubishi Plastics Corporation, DIAFOIL MRQ, thickness 75 μm), the film thickness after drying of the adhesive composition 4 was similarly adjusted to 20 to 30 μm. After applying the above-mentioned coating liquid for the adhesive layer in the form of μm, dry it at 80°C for 5 minutes. This was cured at 23°C for 7 days to allow the cross-linking agent to react, thereby producing an adhesive layer sheet (β'). Peel off and remove the PET films on both sides of the middle layer resin sheet (α) in sequence, and attach the adhesive surfaces of the adhesive layer resin sheets (β) and (β') to the middle layer sheet in sequence. On both surfaces of (α), a laminate (thickness 150 μm) containing (β)/(α)/(β') was produced. Through the PET film remaining on the surface of (β) and (β'), use a high-pressure mercury lamp so that the cumulative light intensity at 365 nm becomes 1000 mJ/cm 2 and the cumulative light intensity at 405 nm becomes 1400 mJ/cm 2 Light is irradiated to photo-crosslink the intermediate layer resin sheet (α), thereby producing the adhesive sheet laminated body 3 . [Example 1-4] A release film coated with a polysiloxy release agent on a PET film (thickness 100 μm) with a UV absorber was used instead of a peeled polyethylene terephthalate film ( DIAFOIL MRV, thickness 100 μm), except for this, the adhesive sheet laminate 4 was produced in the same manner as in Example 1-1. [Example 1-5] On the surface of the polyethylene terephthalate film (DIAFOIL MRV, thickness 100 μm) of the adhesive sheet laminate produced in Example 1-1, the laminate includes a micro-adhesive layer (5 μm )/Polyethylene terephthalate film (25 μm)/Ultraviolet absorbing layer (3 μm) and the slightly adhesive layer of the surface protective film are made into a release film/adhesive sheet/release film/surface protective film Composed of adhesive sheet laminate 5. [Comparative Example 1-1] It was produced in the same manner as Example 1-1 except that 15 g of Esacure TZT (C-4) was added as a photopolymerization initiator instead of Esacure KTO46 (C-1). Adhesive sheet laminate 6. The absorption coefficient of the photopolymerization initiator (C-4) at 405 nm is less than 10 (mL/(g∙cm)), which is too low to be measured. [Comparative Example 1-2] An adhesive sheet laminated body 7 was produced in the same manner as in Example 1-2, except that the ultraviolet absorber (D-2) was not added. [Comparative Example 1-3] A commercially available adhesive solution containing an acrylic copolymer (A-4, mass average molecular weight 1.3 million) (SK-Dyne 1882 manufactured by Soken Chemical Co., Ltd., solid content concentration approximately 17%) 1 kg, add 1.85 g of L-45 (B-5) (manufactured by Soken Chemical Co., Ltd.) as an isocyanate cross-linking agent and 0.5 g of E-5XM (B-6) (manufactured by Soken Chemical Co., Ltd.) as an epoxy cross-linking agent. g. 10 g of 2,2'-dihydroxy-4-methoxybenzophenone (manufactured by Chemipro Kasei, Kemisorb 111) (D-3) as the ultraviolet absorber (D), and mix it evenly to make an adhesive Agent composition 7. Next, the above-mentioned adhesive composition was applied on a peeled polyethylene terephthalate film (DIAFOIL MRV, manufactured by Mitsubishi Plastics Corporation, thickness 100 μm) so that the thickness after drying became 50 μm. Dry at 80°C for 5 minutes to obtain a sheet-like adhesive composition 7 with a thickness of 50 μm. On a peeled polyethylene terephthalate film (DIAFOIL MRQ, manufactured by Mitsubishi Plastics Corporation, thickness 75 μm), the film was coated in the same manner so that the thickness after drying became 50 μm, and then dried at 80°C Dry for 5 minutes to obtain a sheet-like adhesive composition 7 with a thickness of 50 μm. These layers were laminated to a thickness of 100 μm and then covered with a release-treated polyethylene terephthalate film (DIAFOIL MRQ, thickness 75 μm, manufactured by Mitsubishi Plastics Corporation). This was cured at room temperature (23° C.) for 7 days to allow the cross-linking agent to react, thereby producing an adhesive sheet laminate 8. <Evaluation> [Optical Properties] The PET films on both sides of the adhesive sheet laminate produced in Examples 1-1 to 1-5 and Comparative Examples 1-1 to 1-3 were peeled off in order and sandwiched between two sheets of sodium The adhesive sheet is attached between calcium glass (thickness 0.5 mm) and subjected to autoclave treatment (70°C, gauge pressure 0.2 MPa, 20 minutes) for precise attachment. Adhesive sheet laminates 1, 2, 4, 5, 6, and 7 were produced by irradiating light with a high-pressure mercury lamp separated by a UV cutting filter so that the cumulative light intensity at a wavelength of 405 nm became 3000 mJ/cm 2 Samples for optical property evaluation. The light transmittance of the prepared test piece in the wavelength range of 360 to 430 nm was measured with a spectrophotometer (manufactured by Shimadzu Corporation, machine name "UV2450"). Those with a light transmittance of less than 50% at 380 nm are judged as UV absorbance "○ (good)", and those with a transmittance of more than 50% are judged as "× (poor)". The results are shown in Table 1. [Adhesion] Regarding the adhesive sheets produced in Examples 1-1 to 1-5 and Comparative Examples 1-1 to 1-3, a release film was peeled off, and the backing film was assembled using a hand roller. An ethylene phthalate film (manufactured by Toyobo Co., Ltd., trade name "COSMOSHINE A4300", thickness 100 μm) was rolled and bonded. Cut it into short strips of 10 mm wide x 100 mm long, and use a hand roller to peel off the remaining release film and attach the exposed adhesive surface to the soda-lime glass. After performing an autoclave treatment (70°C, gauge pressure 0.2 MPa, 20 minutes) for precise attachment, use high pressure with a UV cutting filter for the adhesive sheet laminates 1, 2, 4, 5, 6, and 7. A mercury lamp is used to irradiate visible light in such a way that the accumulated light amount at a wavelength of 405 nm becomes 3000 mJ/cm 2 and the accumulated light amount at a wavelength of 365 nm becomes 5 mJ/cm 2 or less to prepare an adhesion measurement sample. While stretching the backing film at an angle of 180° at a peeling speed of 60 mm/min, peel off the adhesive sheet from the glass. Use a load cell to measure the tensile strength and measure the 180° peel strength of the adhesive sheet to the glass (N/cm ), expressed as "glass adhesion strength" in Table 1. The results are shown in Table 1. [Absorptiveness of concavity and convexity] Print a 20-μm-thick glass on its peripheral edge (long side 3 mm, short side 15 mm) of 58 mm × 110 mm × 0.8 mm thickness, and prepare an opening of 52 mm × 80 mm. Glass plate with printed steps 1. Also, perform printing with a thickness of 10 μm on the peripheral portion (long side 3 mm, short side 15 mm) of 58 mm × 110 mm × 0.8 mm thick glass, and prepare a printing step with an opening of 52 mm × 80 mm. Poor glass plate 2. Peel off the release film from the adhesive sheet laminate, and roll it onto a piece of soda-lime glass with a thickness of 54 mm x 82 mm and a thickness of 0.5 mm. Secondly, peel off the remaining release film, and use a vacuum press to press and bond the printed surfaces of the glass plates 1 and 2 with printed steps by applying the four sides of the adhesive surface to the printed steps ( Absolute pressure 5 kPa, temperature 70°C, pressurization pressure 0.04 MPa), and autoclave treatment (70°C, gauge pressure 0.2 MPa, 20 minutes) for precise attachment. Regarding the adhesive sheet laminates 1, 2, 4, 5, 6, and 7, from the printed glass side, a high-pressure mercury lamp with a UV cutting filter was used to achieve an accumulated light intensity of 3000 mJ/cm 2 at a wavelength of 405 nm. Light irradiation was carried out to prepare a sample for evaluation. Regarding the above-mentioned evaluation samples, those that can be bonded without bubbles near the step of the glass plate 1 with a printing step of 20 μm are judged to be “◎ (excellent)” in unevenness absorbability, and those with a printing step of 10 μm are judged as If the glass plate 2 with a step difference can be bonded without bubbles near the step difference, it will be judged as "○ (good)" in uneven absorption. Glass plates 1 and 2 with printed steps will be judged as if bubbles are seen near the step difference. The uneven absorption is "× (poor)". The results are shown in Table 1. [Heat resistance] The release film on one side of the adhesive sheet produced in Examples 1-1 to 1-5 and Comparative Examples 1-1 to 1-3 was peeled off, and COP was attached to the exposed surface using a hand roller. Membrane (manufactured by Zeon Co., Ltd., Japan, 100 μm). Secondly, cut the above-mentioned adhesive sheet into 50 mm × 80 mm, peel off the remaining release film, and use a hand roller to attach it to soda-lime glass with a thickness of 0.5 mm, and perform autoclave treatment (temperature 80°C, air pressure 0.4 MPa) , 30 minutes). Regarding the adhesive sheet laminates 1, 2, 4, 5, 6, and 7, use a high-pressure mercury lamp with a UV cutting filter separated from the COP surface so that the cumulative light intensity at a wavelength of 405 nm becomes 3000 mJ/cm 2 irradiate to prepare a sample for evaluation. Regarding the above-mentioned evaluation samples, after curing at 85°C for 6 hours, if there is no foaming, etc. and no change in appearance is seen, the heat resistance is judged as "○ (good)", and if foaming or peeling is seen, the heat resistance is judged as " × (poor)". The results are shown in Table 1. [Light resistance] Peel off the release film of one of the adhesive sheet laminates and laminate it to a 150 mm x 200 mm thick soda-lime glass with a thickness of 2 mm. Secondly, peel off the remaining release film, laminate the exposed adhesive surface to a 150 mm × 200 mm soda-lime glass with a thickness of 2 mm, and perform autoclave treatment (temperature 80°C, air pressure 0.4 MPa, 30 minutes). Adhesive sheet laminates 1, 2, 4, 5, 6, and 7 were irradiated with light using a high-pressure mercury lamp so that the cumulative light intensity at a wavelength of 405 nm became 3000 mJ/cm 2 to prepare samples for evaluation. The above-mentioned evaluation samples were irradiated with ultraviolet rays for 24 hours using a xenon light resistance tester (Suntest CPS, manufactured by ATLAS Co., Ltd.). The light resistance was judged to be "○ (good)" if no bulges were seen on the adhesive sheet, and if bulges or the like were seen. Those who peeled off were judged to have "× (poor)" light resistance. The results are shown in Table 1. [Table 1] Example 1-1 Example 1-2 Example 1-3 Examples 1-4 Examples 1-5 Comparative example 1-1 Comparative example 1-2 Comparative Example 1-3 middle layer Next layer Acrylic copolymer A-1 100 100 100 100 A-2 100 100 A-3 100 A-4 100 100 Cross-linking agent B-1 10 10 10 10 B-2 5 5 B-3 20 L-45 1.85 1.85 E-5XM 0.5 0.5 photoinitiator C-1 1.5 1.5 1.5 C-2 1 1 C-3 0.7 C-4 1.5 UV absorber D-1 0.5 0.5 0.5 0.5 D-2 2 D-3 1 1 Remarks Laminated composition UV cut PET UV cutting protective film Absorption coefficient of photoinitiator (405 nm) mL/(g∙cm) 7.4×10 1 1.6×10 2 9.0×10 2 7.4×10 1 7.4×10 1 <10 1.6×10 2 - glass adhesion N/cm 8 4 10 8 8 2 4 5 Adhesive sheet transmittance (%) 350nm 0 0 0 0 0 0 80 0 360nm 1 0 0 1 1 1 84 0 370nm 11 2 0 11 11 11 86 0 380nm 44 17 3 44 44 44 86 1 390nm 71 55 19 71 71 71 88 13 400nm 81 77 51 81 81 81 88 42 410nm 87 86 77 87 87 87 89 73 420nm 89 89 87 89 89 89 89 86 430nm 89 89 89 89 89 89 89 89 UV absorbency 〇 〇 〇 〇 〇 〇 × 〇 Fit reliability Concave-convex absorbency ◎ ◎ 〇 ◎ ◎ ◎ ◎ × heat resistance 〇 〇 〇 〇 〇 × 〇 〇 Lightfastness 〇 〇 〇 〇 〇 〇 × 〇 Comprehensive evaluation 〇 〇 〇 〇 〇 〇 × × Regarding the peel-treated polyethylene terephthalate film (manufactured by Mitsubishi Plastics Corporation, DIAFOIL MRV, thickness 100 μm) used in Example 1-1, and the film with added ultraviolet absorber used in Example 1-4 PET film (thickness 100 μm), a release film coated with a polysilicone release agent, and a surface protective film used in Examples 1-5, were measured using a spectrophotometer (manufactured by Shimadzu Corporation, machine name "UV2450") measures the light transmittance in the wavelength range 380~450 nm. The results are shown in Table 2. The adhesive sheet laminated body 1, the adhesive sheet laminated body 4, and the adhesive sheet laminated body 5 were each made of a peel-processed polyethylene terephthalate film (made by Mitsubishi Plastics Corporation, DIAFOIL MRV, thickness 100 μm), Example The release film and surface protection film used in 1-4 are placed on the PET film (thickness 100 μm) with UV absorber coated with polysiloxane release agent facing up. The film side was irradiated with light from a fluorescent lamp (illuminance: 1100Lx) for 7 days. The cumulative light amount at the wavelength of 405 nm of the irradiated light is approximately 43 J/cm 2 , and the cumulative light amount at the wavelength of 365 nm is approximately 1 mJ/cm 2 or less, which cannot be measured. Regarding the adhesive sheet laminates 1 and 4 before and after the light irradiation treatment, the gel fraction of the adhesive material was determined by the following method. The results are shown in Table 2. 1) Weigh the adhesive composition (W1) and wrap it in the SUS mesh (W0) with a pre-measured weight. 2) Dip the above SUS mesh into 100 mL of ethyl acetate for 24 hours. 3) Take out the SUS mesh and semi-dry it at 75°C for 4 hours. 4) Calculate the dry weight (W2) and measure the gel fraction of the adhesive composition according to the following formula. Gel fraction (%) = 100 × (W2-W0)/W1 Regarding storage stability, if the change in gel fraction does not reach 5 points before and after fluorescent lamp irradiation, it will be judged as "○ (good)". Those whose gel fraction increased by more than 5 points after light irradiation were judged as "× (poor)". The results are shown in Table 2. [Table 2] Example 1-1 Examples 1-4 Examples 1-5 Release PET light transmittance (%) 380nm 84 26 0 390nm 85 33 0 400nm 86 twenty three 0 410nm 86 13 1 420nm 87 5 9 430nm 87 3 39 440nm 88 2 69 450nm 88 1 81 gel fraction before light exposure 0% 0% 0% After light exposure 68% 2% 0% Storage stability × 〇 〇 The adhesive sheet lamination systems of Examples 1-1 to 1-5 not only have excellent ultraviolet absorption performance, but also have excellent qualities that take into account the uneven absorption during lamination or the reliability of the components after lamination. In contrast, Comparative Example 1-1 uses a photopolymerization initiator whose absorbance coefficient at a wavelength of 405 nm is less than 10 mL/(g∙cm). Therefore, the absorbance coefficient at a wavelength of 405 nm is 10 mL. / (g∙cm) or more of photopolymerization initiator, so even if it is irradiated with light, the adhesive material will not harden, and the adhesive force after the second attachment or the reliability after the joint cannot be obtained. Comparative Example 1-2 does not contain the ultraviolet absorber (D) and cannot obtain ultraviolet absorption performance. Therefore, foaming of the adhesive sheet was seen in the light resistance test, indicating poor bonding reliability. Comparative Examples 1-3 are adhesive sheets in which the adhesive material composition is cross-linked by thermal cross-linking. Since it does not have a photohardenable layer, the uneven absorption during bonding is poor. In addition, in Examples 1-4, a PET film containing an ultraviolet absorber was used as a release film. This can suppress the progression of the photocuring reaction of the adhesive composition before being bonded to a member, and can produce an adhesive sheet laminate with excellent storage stability. Furthermore, in Examples 1-5, a surface protective film having an ultraviolet absorbing layer was laminated on the surface of the release film. This can suppress the progression of the photocuring reaction of the adhesive composition before being bonded to a member, and can produce an adhesive sheet laminate with excellent storage stability. Hereinafter, Examples 2-1 to 2-3 and Comparative Examples 2-1 to 2-2 will be described in further detail. However, the present invention is not limited to these. In addition, the composition of the adhesive resin composition of each layer used in the following Examples and Comparative Examples is shown in Table 3. [Example 2-1] A (meth)acrylic copolymer (2-A) containing 76 parts by mass of 2-ethylhexyl (meth)acrylate, 20 parts by mass of vinyl acetate, and 4 parts by mass of acrylic acid 1 kg of copolymer (2-A-1, mass average molecular weight 400,000), and propoxypentaerythritol tetraacrylate (manufactured by Shin-Nakamura Chemical Co., Ltd., ATM-4P) as a cross-linking agent (2-B) (2- B-1) 200 g, Irgacure 369 (2-C-1) (manufactured by BASF) as photopolymerization initiator (2-C) 8 g, 2,2' as ultraviolet absorber (2-D) 10 g of dihydroxy-4-methoxybenzophenone (Kemisorb 111 manufactured by Chemipro Kasei Co., Ltd.) (2-D-1) was mixed evenly to obtain an adhesive resin composition 2-1. The absorption coefficient at 405 nm of the photopolymerization initiator (2-C-1) is 1.6×10 2 mL/(g∙cm). The adhesive resin composition 2-1 is sandwiched between two peel-processed polyethylene terephthalate films (DIAFOIL MRF, thickness 75 μm, manufactured by Mitsubishi Plastics Corporation/DIAFOIL MRT, thickness 38 μm, manufactured by Mitsubishi Plastics Corporation). , and formed it into a sheet shape so that the thickness becomes 110 μm, to prepare an intermediate layer sheet (α-1). To 1 kg of a commercially available adhesive solution containing an acrylic copolymer (2-A-2, mass average molecular weight 1.3 million) (manufactured by Soken Chemical Co., Ltd., SK-Dyne 1882, solid content concentration approximately 17%), add as isocyanate 1.85 g of L-45 (2-B-2) (manufactured by Soken Chemical Co., Ltd.) as a cross-linking agent and 0.5 g of E-5XM (2-B-3) (manufactured by Soken Chemical Co., Ltd.) as an epoxy cross-linking agent , prepare adhesive resin composition 2. After applying the coating liquid for the adhesive layer on a peeled polyethylene terephthalate film (DIAFOIL MRV manufactured by Mitsubishi Plastics Corporation, thickness 100 μm) so that the thickness after drying becomes 20 μm , dried at 80° C. for 5 minutes to thermally harden the β layer, to prepare a surface layer sheet (β-1). Furthermore, on the peeled polyethylene terephthalate film (DIAFOIL MRQ, manufactured by Mitsubishi Plastics Corporation, thickness 75 μm), the adhesive resin composition was applied in the same manner so that the thickness after drying became 20 μm. After product 2, it was dried at 80° C. for 5 minutes to thermally harden the β layer, and a surface layer sheet (β'-1) was produced. Peel off and remove the PET films on both sides of the middle layer sheet (α-1) in sequence, and attach the adhesive surfaces of the surface layer sheets (β-1) and (β'-1) to the two surfaces in sequence. A laminate containing (β-1)/(α-1)/(β'-1) is produced. Through the PET film remaining on the surface of (β-1) and (β'-1), irradiate with a high-pressure mercury lamp so that the cumulative light intensity at a wavelength of 405 nm becomes 1500 mJ/cm 2 to harden the α layer and create a transparent Double-sided adhesive sheet laminate 2-1 (thickness: 150 μm). [Example 2-2] 200 g of cross-linking agent (2-B-1) was added to 1 kg of (meth)acrylic copolymer (2-A-1) as a photopolymerization initiator (2-C) 20 g of Esacure KTO46 (2-C-2) (manufactured by Lanberti Company) and 20 g of ultraviolet absorber (2-D-1) were mixed evenly to obtain adhesive resin composition 2-3. The absorption coefficient of the photopolymerization initiator (2-C-2) at 405 nm is 7.4×10 1 mL/(g∙cm). The adhesive resin composition 2-3 is sandwiched between two peel-processed polyethylene terephthalate films (DIAFOIL MRF manufactured by Mitsubishi Plastics Corporation, thickness 75 μm/DIAFOIL MRT manufactured by Mitsubishi Plastics Corporation, thickness 38 μm). , and formed it into a sheet shape so that the thickness becomes 60 μm, to prepare an intermediate layer sheet (α-2). In the same manner as in Example 2-1, the PET films on both sides of the intermediate layer sheet (α-2) were peeled off and removed in sequence, and the adhesive layers of the surface layer sheets (β-1) and (β'-1) were removed. The surfaces are sequentially bonded to the two surfaces to create a laminate containing (β-1)/(α-2)/(β'-1). Through the PET film remaining on the surface of (β-1) and (β'-1), irradiate with a high-pressure mercury lamp so that the cumulative light intensity at a wavelength of 405 nm becomes 3000 mJ/cm 2 to harden the α layer and create a transparent Double-sided adhesive sheet laminate 2-2 (thickness: 100 μm). [Example 2-3] 200 g of cross-linking agent (2-B-1) and photopolymerization initiator (2-C-2) were added to 1 kg of (meth)acrylic copolymer (2-A-1). ) 8 g and ultraviolet absorber (2-D-1) 20 g, and mix them evenly to obtain adhesive resin composition 2-4. The adhesive resin composition 2-4 is sandwiched between two peel-processed polyethylene terephthalate films (DIAFOIL MRF, thickness 75 μm, manufactured by Mitsubishi Plastics Corporation/DIAFOIL MRT, thickness 38 μm, manufactured by Mitsubishi Plastics Corporation). , and shaped it into a sheet shape so that the thickness becomes 60 μm, to produce an intermediate layer sheet (α-3). In the same manner as in Example 2-1, the PET films on both sides of the intermediate layer sheet (α-3) were peeled off and removed in sequence, and the adhesive layers of the surface layer sheets (β-1) and (β'-1) were removed. The surfaces are bonded to both sides in order to create a laminate containing (β-1)/(α-3)/(β'-1). Through the PET film remaining on the surface of (β-1) and (β'-1), irradiate with a high-pressure mercury lamp so that the cumulative light intensity at a wavelength of 405 nm becomes 3000 mJ/cm 2 to harden the α layer and create a transparent Double-sided adhesive sheet laminate 2-3 (thickness 100 μm). [Comparative Example 2-1] To 1 kg of (meth)acrylic copolymer (2-A-1), 200 g of cross-linking agent (2-B-1) was added as a photopolymerization initiator (2-C ) 10 g of Esacure TZT (2-C-3) (manufactured by Lanberti Co., Ltd.), 2,2'-dihydroxy-4-methoxybenzophenone (Chemipro Kasei Co., Ltd.) as ultraviolet absorber (2-D) Manufacture, Kemisorb 111) (2-D-1) 20 g, and mix evenly to obtain adhesive resin composition 2-5. The absorption coefficient of the photopolymerization initiator (2-C-3) at 405 nm does not reach 10 mL/(g∙cm), which is too low to be measured. The adhesive resin composition 2-5 was sandwiched between two peel-processed polyethylene terephthalate films (DIAFOIL MRF, thickness 75 μm, manufactured by Mitsubishi Plastics Corporation/DIAFOIL MRT, thickness 38 μm, manufactured by Mitsubishi Plastics Corporation). , and shaped it into a sheet shape so that the thickness becomes 110 μm, to produce an intermediate layer sheet (α-4). In the same manner as in Example 2-1, the PET films on both sides of the intermediate layer sheet (α-4) were peeled off and removed in sequence, and the surface layer sheets (β-1) and (β'-1) were adhered The surfaces are sequentially bonded to the two surfaces to create a laminate containing (β-1)/(α-4)/(β'-1). Through the PET film remaining on the surface of (β-1) and (β'-1), irradiate with a high-pressure mercury lamp so that the cumulative light intensity at a wavelength of 405 nm becomes 1500 mJ/cm 2 to harden the α layer and create a transparent Double-sided adhesive sheet laminate 2-4 (thickness 100 μm). [Comparative Example 2-2] To 1 kg of (meth)acrylic copolymer (2-A-1), 200 g of cross-linking agent (2-B-1) and photopolymerization initiator (2-C- 2) 8 g and mix evenly to obtain adhesive resin composition 2-6. At this time, the ultraviolet absorber (2-D) was not added. The adhesive resin composition 2-6 is sandwiched between two peel-processed polyethylene terephthalate films (DIAFOIL MRF, thickness 75 μm, manufactured by Mitsubishi Plastics Corporation/DIAFOIL MRT, thickness 38 μm, manufactured by Mitsubishi Plastics Corporation). , and formed it into a sheet shape so that the thickness becomes 110 μm, to produce an intermediate layer sheet (α-5). In the same manner as in Example 2-1, the PET films on both sides of the intermediate layer sheet (α-5) were peeled off and removed in sequence, and the adhesive layers of the surface layer sheets (β-1) and (β'-1) were removed. The surfaces are sequentially bonded to the two surfaces to create a laminate containing (β-1)/(α-5)/(β'-1). Through the PET film remaining on the surface of (β-1) and (β'-1), irradiate with a high-pressure mercury lamp so that the cumulative light intensity at a wavelength of 405 nm becomes 1500 mJ/cm 2 to harden the α layer and create a transparent Double-sided adhesive sheet laminate 2-5 (thickness 150 μm). <Evaluation> [Ultraviolet absorption performance] The PET films on both sides of the transparent double-sided adhesive sheet laminate produced in Examples 2-1 to 2-3 and Comparative Examples 2-1 to 2-2 were peeled off in sequence, and sandwiched After attaching the adhesive sheet between two pieces of soda-lime glass (54×82 mm, thickness 0.5 mm), perform autoclave treatment (70°C, gauge pressure 0.2 MPa, 20 minutes) for precise attachment as a UV absorber Samples for performance evaluation. The light transmittance of the prepared test piece in the wavelength range of 360 to 430 nm was measured with a spectrophotometer (manufactured by Shimadzu Corporation, machine name "UV2450"). Those with a light transmittance of less than 50% at 380 nm are judged as "○ (good)", and those with a light transmittance of 50% or more are judged as "× (poor)". The results are shown in Table 4. [Glass Adhesion] Regarding the transparent double-sided adhesive sheets produced in Examples 2-1 to 2-3 and Comparative Examples 2-1 to 2-2, peel off a release film and use a hand roller to remove the polyester film as the backing film. The ethylene terephthalate film (manufactured by Toyobo Co., Ltd., trade name "COSMOSHINE A4300", thickness 100 μm) was bonded by roller. Cut it into short strips of 10 mm wide × 100 mm long, and use a hand roller to peel off the remaining release film and attach the exposed adhesive surface to the soda-lime glass. This was subjected to autoclave treatment (70°C, gauge pressure 0.2 MPa, 20 minutes) for precise adhesion, and a sample for adhesion measurement was prepared. While stretching the backing film at an angle of 180° at a peeling speed of 60 mm/min, the adhesive sheet was peeled off from the glass. The tensile strength was measured using a load cell, and the 180° peel strength of the adhesive sheet to the glass was measured. The results Shown in Table 4. [Retention force (offset length)] After cutting the adhesive sheets produced in Examples 2-1 to 2-3 and Comparative Examples 2-1 to 2-2 into 50 mm × 100 mm, peel off the release film on one side. , use a hand roller to attach the adhesive sheet by overlapping one side of the adhesive sheet with the polyethylene terephthalate film (thickness 38 μm) as the substrate, and cut it into a short piece of 25 mm wide x 100 mm long Strips are used as test pieces. Next, the remaining release film was peeled off, and the test piece was attached with a hand roller so as to overlap a vertically erected SUS plate (thickness 120 mm, 5 mm × 1.5 mm) by a length of 20 mm. At this time, the attachment area of the transparent double-sided adhesive sheet and the SUS board becomes 25 mm × 20 mm. After that, the test piece was cured in an atmosphere of 40°C for 15 minutes. The test piece was installed in the vertical direction and a weight of 500 g was applied. After leaving it for 30 minutes, the attached position of the SUS and the test piece was measured downward. offset length (mm). Those with a deviation length of less than 1 mm are judged as "◎ (excellent)", those with a deviation length of 1 mm or more and less than 2 mm are judged as "0 (good)", and those with a deviation length of 2 mm or more are judged as "◎(Excellent)" It was judged as "× (poor)". The results are shown in Table 4. [Foaming Resistance Reliability] As a sample for foaming resistance reliability evaluation, two pieces that were identical to the sample for ultraviolet absorption performance evaluation were used. This was cured at 85° C. for 100 hours, and those with no foaming, etc. and no change in appearance were judged as "○ (good)", and those with foaming or peeling were judged as "× (poor)". The results are shown in Table 4. [table 3] Adhesive resin composition 2-1 2-2 2-3 2-4 2-5 2-6 (Meth)acrylic copolymer (A) A-1 100 100 100 100 100 A-2 100 Cross-linking agent (B) B-1 20 20 20 20 20 B-2 0.185 B-3 0.05 Photopolymerization initiator (C) C-1 0.8 0.8 C-2 2 0.8 C-3 1 UV absorber(D) D-1 1 2 2 2 Photopolymerization initiator (C) Absorption coefficient 405nm 1.6×10 2 - 7.4×10 1 7.4×10 1 <10 1.6×10 2 [Table 4] Example 2-1 Example 2-2 Example 2-3 Comparative example 2-1 Comparative example 2-2 Transmittance[%] 360nm 0 0 0 0 84 370nm 0 0 0 0 85 380nm 3 4 3 3 88 390nm 19 twenty one 18 20 88 400nm 51 53 52 53 89 410nm 77 78 78 79 89 420nm 87 87 87 88 89 430nm 89 89 89 89 89 UV absorption properties 〇 〇 〇 〇 × Glass adhesion strength [N/cm] 10 9 10 2 7 Holding power(40℃) ◎ (1mm) ◎ (1mm) 〇(1.9mm) × (fall) ◎ (＜1mm) Foaming resistance reliability 〇 〇 〇 × 〇 Comprehensive evaluation ◎ ◎ 〇 × × When the adhesive sheet laminates of Examples 2-1 to 2-3 were observed, no bleeding of the ultraviolet absorber (D) was observed. The adhesive sheet lamination system of Examples 2-1 to 2-3 maintains properties such as adhesion or holding power, moisture and heat resistance reliability, and provides excellent ultraviolet absorption properties. Comparative Example 2-1 uses a photopolymerization initiator with an absorbance coefficient of less than 10 mL/(g∙cm) at a wavelength of 405 nm, so even if it is irradiated with light, the adhesive will not harden, and the adhesive strength will be reduced after bonding. Reliability is poor. In Comparative Example 2-2, since the α layer does not contain the ultraviolet absorber (D), the ultraviolet absorption performance is poor.

Claims (16)

一種透明雙面黏著片，其係用於介隔於2個圖像顯示裝置構成構件之間並積層該等構件者，該透明雙面黏著片包含黏著劑樹脂組合物，該黏著劑樹脂組合物含有(甲基)丙烯酸系共聚物(A)、交聯劑(B)、波長405nm之吸光係數為10mL/(g．cm)以上之光聚合起始劑(C)及紫外線吸收劑(D)，紫外線吸收劑(D)具有選自由三
Figure 110104305-A0305-02-0055-2
結構及二苯甲酮結構所組成之群中之1種或2種以上之結構，相對於光聚合起始劑(C)100質量份以25~400質量份之比率含有紫外線吸收劑(D)，上述圖像顯示裝置構成構件係包含由觸控感測器、圖像顯示面板、表面保護面板及偏光膜所組成之群中之任一種或兩種以上之組合而成之積層體。 A transparent double-sided adhesive sheet for interposing between two components of an image display device and laminating the components. The transparent double-sided adhesive sheet contains an adhesive resin composition. The adhesive resin composition Contains (meth)acrylic copolymer (A), cross-linking agent (B), photopolymerization initiator (C) with an absorption coefficient of 10 mL/(g.cm) or more at a wavelength of 405 nm, and ultraviolet absorber (D) , the ultraviolet absorber (D) has a material selected from three
Figure 110104305-A0305-02-0055-2
One or more structures in the group consisting of a structure and a benzophenone structure, containing an ultraviolet absorber (D) at a ratio of 25 to 400 parts by mass relative to 100 parts by mass of the photopolymerization initiator (C) , The above-mentioned image display device components include a laminate composed of any one or a combination of two or more of the group consisting of a touch sensor, an image display panel, a surface protection panel, and a polarizing film. 如請求項1之透明雙面黏著片，其中(甲基)丙烯酸系共聚物(A)包含具備巨分子單體作為枝成分之接枝共聚物。 The transparent double-sided adhesive sheet of claim 1, wherein the (meth)acrylic copolymer (A) includes a graft copolymer having a macromonomer as a branch component. 如請求項1之透明雙面黏著片，其含有多官能(甲基)丙烯酸酯化合物作為交聯劑(B)。 Such as the transparent double-sided adhesive sheet of claim 1, which contains a multifunctional (meth)acrylate compound as a cross-linking agent (B). 如請求項1之透明雙面黏著片，其含有裂解型光聚合起始劑作為光聚合起始劑(C)。 Such as the transparent double-sided adhesive sheet of claim 1, which contains a cleavage-type photopolymerization initiator as the photopolymerization initiator (C). 如請求項1之透明雙面黏著片，其中上述黏著劑樹脂組合物於室溫(20℃)下顯示黏著性，且於100℃下具備軟化或流體化之性質。 The transparent double-sided adhesive sheet of claim 1, wherein the adhesive resin composition exhibits adhesiveness at room temperature (20°C) and has softening or fluidizing properties at 100°C. 一種黏著片積層體，其具備積層如請求項1至5中任一項之透明雙面黏著片與脫模膜而成之構成。 An adhesive sheet laminated body having a structure in which a transparent double-sided adhesive sheet and a release film according to any one of claims 1 to 5 are laminated. 如請求項6之黏著片積層體，其中上述脫模膜之波長410nm以下之光之透光率為40%以下。 The adhesive sheet laminate of claim 6, wherein the release film has a light transmittance of 40% or less for light having a wavelength of 410 nm or less. 如請求項6或7之黏著片積層體，其具備於上述脫模膜之表面積層波長410nm以下之光之透光率為40%以下之表面保護膜而成之構成。 The adhesive sheet laminate of claim 6 or 7 has a structure in which a surface protective film having a transmittance of 40% or less for light with a wavelength of 410 nm or less is laminated on the surface of the release film. 一種黏著片積層體，其具備積層透明雙面黏著片與膜而成之構成，該透明雙面黏著片係用於介隔於2個圖像顯示裝置構成構件之間並積層該等構件者，並包含含有(甲基)丙烯酸系共聚物(A)、交聯劑(B)、波長405nm下之吸光係數為10mL/(g．cm)以上之光聚合起始劑(C)、以及相對於上述光聚合起始劑(C)100質量份以25~400質量份之比率含有之具有選自由三
Figure 110104305-A0305-02-0056-1
結構及二苯甲酮結構所組成之群中之1種或2種以上之結構之紫外線吸收劑(D)之黏著劑樹脂組合物，其中上述圖像顯示裝置構成構件係包含由觸控感測器、圖像顯示面板、表面保護面板及偏光膜所組成之群中之任一種或兩種以上之組合而成之積層體，該膜之波長380nm以上且410nm以下之光之透光率為40%以下。 An adhesive sheet laminate having a structure in which a transparent double-sided adhesive sheet and a film are laminated, and the transparent double-sided adhesive sheet is used to interpose between two components of an image display device and to laminate the components. It also contains a (meth)acrylic copolymer (A), a cross-linking agent (B), a photopolymerization initiator (C) with an absorption coefficient of 10 mL/(g.cm) or more at a wavelength of 405 nm, and 100 parts by mass of the above-mentioned photopolymerization initiator (C) contains a compound selected from three components in a ratio of 25 to 400 parts by mass.
Figure 110104305-A0305-02-0056-1
An adhesive resin composition of an ultraviolet absorber (D) with one or more structures in the group consisting of a benzophenone structure and a benzophenone structure, wherein the above-mentioned image display device components include a touch sensor A laminate composed of any one or a combination of two or more of the group consisting of a device, an image display panel, a surface protection panel and a polarizing film. The film has a light transmittance of 40 for light with wavelengths above 380 nm and below 410 nm. %the following. 如請求項9之黏著片積層體，其中上述2個圖像顯示裝置構成構件中之至少一個係具備紫外線吸收性能者。 The adhesive sheet laminate of claim 9, wherein at least one of the two image display device components has ultraviolet absorbing properties. 一種圖像顯示裝置，其係使用如請求項9之黏著片積層體而構成。 An image display device constructed using the adhesive sheet laminate of Claim 9. 如請求項11之圖像顯示裝置，其中構成圖像顯示裝置之圖像顯示裝置構成構件中之至少一個係具備紫外線吸收性能者。 The image display device according to claim 11, wherein at least one of the image display device components constituting the image display device has ultraviolet absorbing properties. 一種圖像顯示裝置構成用積層體之製造方法，其特徵在於：其係製造具備經由如請求項1至5中任一項之透明雙面黏著片積層圖像顯示裝置構成構件而成之構成的圖像顯示裝置構成用積層體之方法，且至少具有如下(1)及(2)之步驟：(1)經由包含含有(甲基)丙烯酸系共聚物(A)、交聯劑(B)、及波長405nm下之吸光係數為10mL/(g．cm)以上之光聚合起始劑(C)之黏著劑組合物的光硬化前之透明雙面黏著片，積層2個圖像顯示裝置構成構件之步驟；(2)於經由透明雙面黏著片積層2個圖像顯示裝置構成用構件後，自至少一圖像顯示裝置構成用構件之外側，透過該圖像顯示裝置構成用構件將至少波長405nm之光照射至上述透明雙面黏著片，使該雙面黏著片交聯而硬化之步驟。 A method of manufacturing a laminated body for forming an image display device, characterized by manufacturing a structure in which image display device forming components are laminated via a transparent double-sided adhesive sheet according to any one of claims 1 to 5. A method for constructing a laminate for an image display device, comprising at least the following steps (1) and (2): (1) via a method containing a (meth)acrylic copolymer (A), a cross-linking agent (B), and a transparent double-sided adhesive sheet before light curing of an adhesive composition of a photopolymerization initiator (C) with an absorption coefficient of 10 mL/(g.cm) or more at a wavelength of 405 nm, laminated with two components constituting an image display device Steps; (2) After laminating two image display device constituting members via a transparent double-sided adhesive sheet, at least one wavelength of the image display device constituting member is passed through the image display device constituting member from the outside. The step of irradiating the above-mentioned transparent double-sided adhesive sheet with 405nm light to cross-link and harden the double-sided adhesive sheet. 如請求項13之圖像顯示裝置構成用積層體之製造方法，其中至少波長405nm之光係自包含選自太陽、螢光燈、LED、有機EL、無機EL及圖像 顯示裝置用發光模組中之至少1種或2種以上之組合之光源所照射之光。 The method of manufacturing a laminate for forming an image display device according to claim 13, wherein the light having a wavelength of at least 405 nm is selected from the group consisting of the sun, fluorescent lamps, LEDs, organic EL, inorganic EL and images. The light emitted by at least one or a combination of two or more light sources in the light-emitting module of the display device. 如請求項13或14之圖像顯示裝置構成用積層體之製造方法，其中於上述步驟(1)中，加熱透明雙面黏著片而將2個圖像顯示裝置構成構件積層。 The method of manufacturing a laminated body for forming an image display device according to Claim 13 or 14, wherein in the above step (1), the transparent double-sided adhesive sheet is heated to laminate two components forming the image display device. 如請求項15之圖像顯示裝置構成用積層體之製造方法，其係加熱圖像顯示裝置構成構件中之一者或兩者而加熱透明雙面黏著片。 In the method of manufacturing a laminate for forming an image display device according to Claim 15, one or both of the components constituting the image display device are heated to heat the transparent double-sided adhesive sheet.
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