KR20170091429A - Pressure sensitive adhesive composition, encapsulation sheet for a solarcell having an encapsulating layer comprising the same, and a solar cell module comprising the encapsulation sheet - Google Patents

Pressure sensitive adhesive composition, encapsulation sheet for a solarcell having an encapsulating layer comprising the same, and a solar cell module comprising the encapsulation sheet Download PDF

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KR20170091429A
KR20170091429A KR1020160012445A KR20160012445A KR20170091429A KR 20170091429 A KR20170091429 A KR 20170091429A KR 1020160012445 A KR1020160012445 A KR 1020160012445A KR 20160012445 A KR20160012445 A KR 20160012445A KR 20170091429 A KR20170091429 A KR 20170091429A
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meth
acrylate
sensitive adhesive
parts
adhesive composition
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KR102063056B1 (en
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민지현
김현철
권윤경
박현규
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주식회사 엘지화학
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    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J133/00Adhesives based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Adhesives based on derivatives of such polymers
    • C09J133/04Homopolymers or copolymers of esters
    • C09J133/06Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, the oxygen atom being present only as part of the carboxyl radical
    • C09J133/10Homopolymers or copolymers of methacrylic acid esters
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J11/00Features of adhesives not provided for in group C09J9/00, e.g. additives
    • C09J11/02Non-macromolecular additives
    • C09J11/06Non-macromolecular additives organic
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J133/00Adhesives based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Adhesives based on derivatives of such polymers
    • C09J133/04Homopolymers or copolymers of esters
    • C09J133/06Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, the oxygen atom being present only as part of the carboxyl radical
    • C09J133/08Homopolymers or copolymers of acrylic acid esters
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J133/00Adhesives based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Adhesives based on derivatives of such polymers
    • C09J133/04Homopolymers or copolymers of esters
    • C09J133/06Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, the oxygen atom being present only as part of the carboxyl radical
    • C09J133/10Homopolymers or copolymers of methacrylic acid esters
    • C09J133/12Homopolymers or copolymers of methyl methacrylate
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
    • H01L31/00Semiconductor devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation and specially adapted either for the conversion of the energy of such radiation into electrical energy or for the control of electrical energy by such radiation; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof
    • H01L31/04Semiconductor devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation and specially adapted either for the conversion of the energy of such radiation into electrical energy or for the control of electrical energy by such radiation; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof adapted as photovoltaic [PV] conversion devices
    • H01L31/042PV modules or arrays of single PV cells
    • H01L31/048Encapsulation of modules
    • H01L31/0481Encapsulation of modules characterised by the composition of the encapsulation material
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
    • H01L31/00Semiconductor devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation and specially adapted either for the conversion of the energy of such radiation into electrical energy or for the control of electrical energy by such radiation; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof
    • H01L31/08Semiconductor devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation and specially adapted either for the conversion of the energy of such radiation into electrical energy or for the control of electrical energy by such radiation; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof in which radiation controls flow of current through the device, e.g. photoresistors
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02EREDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E10/00Energy generation through renewable energy sources
    • Y02E10/50Photovoltaic [PV] energy

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  • Physics & Mathematics (AREA)
  • Condensed Matter Physics & Semiconductors (AREA)
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  • Engineering & Computer Science (AREA)
  • Computer Hardware Design (AREA)
  • Microelectronics & Electronic Packaging (AREA)
  • Power Engineering (AREA)
  • Adhesives Or Adhesive Processes (AREA)

Abstract

The present application relates to an adhesive composition, an encapsulation sheet for a solar cell having an encapsulating layer comprising cured materials of the composition, and a solar cell module comprising the encapsulation sheet. According to an exemplary adhesive composition, it is possible to provide an encapsulation layer having excellent mechanical and optical characteristics, and excellent resistance to moisture, heat and ultraviolet rays. In addition, the exemplary adhesive composition of the present application omits vacuum, high-temperature, and high-pressure laminating processes, and can perform a roll to roll continuous process, thereby improving production speed and production efficiency.

Description

점착제 조성물, 그 조성물의 경화물을 포함하는 봉지층을 포함하는 태양전지용 봉지재 시트 및 상기 봉지재 시트를 포함하는 태양전지 모듈{PRESSURE SENSITIVE ADHESIVE COMPOSITION, ENCAPSULATION SHEET FOR A SOLARCELL HAVING AN ENCAPSULATING LAYER COMPRISING THE SAME, AND A SOLAR CELL MODULE COMPRISING THE ENCAPSULATION SHEET}TECHNICAL FIELD [0001] The present invention relates to a pressure-sensitive adhesive composition, a sealing sheet for a solar cell including a sealing layer containing a cured product of the composition, and a solar cell module including the sealing sheet. BACKGROUND OF THE INVENTION [0002] Conventionally, , AND A SOLAR CELL MODULE COMPRISING THE ENCAPSULATION SHEET}

본 출원은 점착제 조성물, 그 조성물의 경화물을 포함하는 봉지층을 포함하는 태양전지용 봉지재 시트 및 상기 봉지재 시트를 포함하는 태양전지 모듈에 관한 것이다.The present invention relates to a pressure-sensitive adhesive composition, a solar cell encapsulant sheet including an encapsulation layer containing a cured product of the composition, and a solar cell module including the encapsulation material sheet.

태양광 발전은 태양광으로부터 전기를 생산하는 청정 발전 기술이다. 태양광 발전 시설은 태양광을 받아 전기를 발생하는 태양전지(모듈)와 발생된 직류 전기를 교류로 변환시키는 전력 조절 장치 및 주간에 생선된 전기를 저장하는 축전지 등으로 구성된다. 전기를 발생시키는 모듈은 일반적으로 유리, 봉지재, 태양전지 및 이면시트로 구성되어 있다.Solar power generation is a clean power generation technology that produces electricity from sunlight. Photovoltaic power generation facilities consist of a solar cell (module) that generates electricity by receiving sunlight, a power regulator that converts the generated direct current into alternating current, and a battery that stores the electricity generated in the daytime. Generally, the module that generates electricity is composed of glass, encapsulant, solar cell, and backsheet.

현재 봉지재로 쓰이는에틸렌-비닐아세테이트 공중합체(EVA)는 습기에 취약한 태양전지 소자를 보호하기 위해 태양전지 전후면과 표면재 사이에 삽입되는 물질이다. EVA는 투과율, 접착력 및 탄성등의 특성을 어느 정도 만족시키나, 진공 및 고온에서의 별도 가교 공정이 필요하여 태양전지 모듈의 생산속도 및 생산효율을 저하시킬 수 있다. 또한, EVA는 가교 시 발생하는 산 등의 부식성 물질과 장기간 자외선 노출에 따른 황변 현상으로 인해 태양전지 모듈의 효율을 저하시키는 문제점이 있다.Currently, ethylene-vinyl acetate copolymer (EVA), which is used as an encapsulant, is a substance that is inserted between the front and rear surfaces of the solar cell and the surface material to protect moisture-sensitive solar cell devices. EVA satisfies the characteristics such as transmittance, adhesive force and elasticity to some extent, but requires a separate crosslinking step in vacuum and high temperature, which may lower the production speed and production efficiency of the solar cell module. In addition, EVA has a problem of deteriorating efficiency of a solar cell module due to corrosive substances such as acid generated during crosslinking and yellowing due to long-term ultraviolet exposure.

본 출원은 상기한 문제점을 해결하기 위한 것으로, 점착제 조성물, 상기 조성물의 경화물을 포함하는 봉지층을 포함하는 태양전지용 봉지재 시트 및 상기 봉지재 시트를 포함하는 태양전지 모듈을 제공하는 것을 목적으로 한다.The present invention has been made to solve the above-mentioned problems, and it is an object of the present invention to provide a solar cell module comprising a pressure-sensitive adhesive composition, a sealing material sheet for a solar cell including a sealing layer containing a cured product of the composition, and the sealing material sheet do.

본 출원은 점착제 조성물에 관한 것이다. 예시적인 상기 점착제 조성물을 이용해 제조한 태양전지용 봉지재 시트는 EVA 시트와 같이 진공 압착 등의 가교 공정(약 15분 소요)을 요구하지 않는다. 또한, 상기 점착제 조성물은 점착액 자체를 도포해 수 분 동안의 열 경화를 진행하여 롤 투 롤(Roll to Roll) 연속 공정을 통해 제작 가능하므로 생산속도 및 생산 효율이 우수하다. 또한, 내습에 강한 소재를 사용하여 EVA 봉지재보다 내습성이 우수하며, EVA와 달리 가교시 산이 발생하지 않아 그로 인한 광전소자의 부식이 없고, UV cut-off 특성을 향상시켜 황변 현상을 억제하였다.The present application relates to a pressure-sensitive adhesive composition. The sealing material sheet for a solar cell manufactured using the exemplary pressure-sensitive adhesive composition does not require a crosslinking step such as vacuum pressing (takes about 15 minutes) like the EVA sheet. In addition, the pressure-sensitive adhesive composition can be produced through a roll-to-roll continuous process by applying the adhesive liquid itself and proceeding thermosetting for several minutes, so that the production speed and production efficiency are excellent. In addition, it is superior in moisture resistance than EVA encapsulant by using material resistant to humidity, and it does not cause acid corrosion due to crosslinking unlike EVA, thereby preventing the deterioration of photoelectric devices and enhancing UV cut-off characteristics to suppress yellowing .

이하에서 본 출원의 태양전지용 봉지재 시트 및 상기 봉지재 시트를 포함하는 태양전지 모듈을 첨부된 도면을 참조하여 구체적으로 설명하지만 첨부된 도면은 예시적인 것으로서, 상기 태양전지 모듈이 예시된 도면에 의하여 제한되는 것은 아니다.Hereinafter, the solar cell module including the solar cell encapsulant sheet and the encapsulation material sheet of the present application will be described in detail with reference to the attached drawings, but the accompanying drawings are exemplary and the solar cell module But is not limited to.

본 출원에 있어서 「박리력」은 전면 부재에 대한 봉지층의 박리력을 의미하며, ASTM D903에 의해 측정된 값을 의미한다.In the present application, the "peeling force" means the peeling force of the sealing layer with respect to the front member, and means the value measured by ASTM D903.

본 출원에 있어서, 「Y.I」 값은 황변지수를 의미하며, ASTM D1003에 의해 측정된 값을 의미한다.In the present application, the value " Y.I " means the yellowing index and means the value measured by ASTM D1003.

본 출원에 있어서, 「투과율」 값은 ASTM D1003에 의해 측정된 값을 의미한다.In the present application, the " transmittance " value means the value measured by ASTM D1003.

본 출원에 있어서, 「Haze」 값은 ASTM D1003에 의해 측정된 값을 의미한다.In the present application, the " Haze " value means the value measured by ASTM D1003.

본 출원의 점착제 조성물은 (메트)아크릴레이트와 반응형 자외선 안정제의 공중합체를 포함하는 점착성 중합체; 및 파장변환물질을 포함한다.The pressure sensitive adhesive composition of the present application comprises a pressure sensitive adhesive polymer comprising a copolymer of (meth) acrylate and a reactive ultraviolet stabilizer; And a wavelength conversion material.

상기 (메트)아크릴레이트는 가교성 관능기를 포함하는 (메트)아크릴레이트 및 알킬(메트)아크릴레이트를 의미하며, 하나의 예시에서 본 출원의 점착제 조성물은 가교성 관능기를 포함하는 (메트)아크릴레이트와 알킬(메트)아크릴레이트를 모두 포함할 수 있다.The (meth) acrylate refers to a (meth) acrylate and an alkyl (meth) acrylate containing a crosslinkable functional group. In one example, the pressure sensitive adhesive composition of the present application comprises (meth) acrylate containing a crosslinkable functional group And alkyl (meth) acrylate.

가교성 관능기를 포함하는 (메트)아크릴레이트의 가교성 관능기는 히드록시기일 수 있다. 히드록시기를 포함하는 (메트)아크릴레이트는 예를 들면, 2-히드록시에틸 (메트)아크릴레이트, 2-히드록시프로필(메트)아크릴레이트, 4-히드록시부틸 (메트)아크릴레이트, 6-히드록시헥실 (메트)아크릴레이트 또는 8-히드록시옥틸 (메트)아크릴레이트 등의 히드록시알킬 (메트)아크릴레이트; 또는 2-히드록시에틸렌글리콜 (메트)아크릴레이트 또는 2-히드록시프로필렌글리콜 (메트)아크릴레이트 등의 히드록시알킬렌글리콜 (메트)아크릴레이트 등이 사용될 수 있으나, 이에 제한되는 것은 아니다.The crosslinkable functional group of the (meth) acrylate containing a crosslinkable functional group may be a hydroxy group. Examples of the (meth) acrylate containing a hydroxy group include 2-hydroxyethyl (meth) acrylate, 2-hydroxypropyl (meth) acrylate, 4-hydroxybutyl Hydroxyalkyl (meth) acrylates such as hydroxyhexyl (meth) acrylate or 8-hydroxyoctyl (meth) acrylate; Or hydroxyalkylene glycol (meth) acrylate such as 2-hydroxyethyleneglycol (meth) acrylate or 2-hydroxypropyleneglycol (meth) acrylate, but is not limited thereto.

알킬(메트)아크릴레이트는 예를 들면, 탄소수 1 내지 20, 탄소수 1 내지 15 또는 탄소수 1 내지 10의 알킬기를 가지는 알킬 (메트)아크릴레이트를 사용할 수 있다. 상기에서 알킬기는, 예를 들면, 직쇄형, 분지쇄형 또는 고리형일 수 있다. 이러한 단량체의 예로는 메틸 (메트)아크릴레이트, 에틸 (메트)아크릴레이트, n-프로필 (메트)아크릴레이트, 이소프로필 (메트)아크릴레이트, n-부틸 (메트)아크릴레이트, sec-부틸 (메트)아크릴레이트, 2-메틸 헵실 (메트)아크릴레이트, 펜틸 (메트)아크릴레이트, 2-에틸헥실 (메트)아크릴레이트, 2-에틸부틸 (메트)아크릴레이트, n-옥틸 (메트)아크릴레이트, 이소보닐(메트)아크릴레이트 등을 들 수 있고, 상기 중 일종 또는 이종 이상을 선택하여 사용할 수 있지만 이에 제한되는 것은 아니다.As the alkyl (meth) acrylate, for example, alkyl (meth) acrylates having an alkyl group having 1 to 20 carbon atoms, 1 to 15 carbon atoms, or 1 to 10 carbon atoms can be used. The alkyl group in the above may be, for example, straight chain, branched chain or cyclic. Examples of such monomers are methyl (meth) acrylate, ethyl (meth) acrylate, n-propyl (meth) acrylate, isopropyl (meth) acrylate, Acrylate, 2-ethylhexyl (meth) acrylate, 2-ethylbutyl (meth) acrylate, n-octyl (meth) acrylate, Isobornyl (meth) acrylate, and the like, and one or more of the above can be selected and used, but the present invention is not limited thereto.

가교성 관능기를 포함하는 (메트)아크릴레이트는 알킬(메트)아크릴레이트 및 가교성 관능기를 포함하는 (메트)아크릴레이트 100 중량부에 대하여 3 내지 30 중량부, 4 내지 20 중량부 또는 5 내지 15 중량부일 수 있다. 상기 범위에서, 점착제 조성물로 형성한 봉지층이 우수한 기계적 특성을 나타낼 수 있다.(Meth) acrylate containing a crosslinkable functional group is used in an amount of 3 to 30 parts by weight, 4 to 20 parts by weight, or 5 to 15 parts by weight, based on 100 parts by weight of (meth) acrylate containing an alkyl (meth) acrylate and a crosslinkable functional group. Weight portion. In the above range, the sealing layer formed from the pressure-sensitive adhesive composition can exhibit excellent mechanical properties.

본 출원의 점착제 조성물은 반응형 자외선 안정제를 포함한다. 하나의 예시에서, 반응형 자외선 안정제는 하기 화학식 1로 나타내어지는 아크릴계 단량체일 수 있다.The pressure-sensitive adhesive composition of the present application includes a reactive ultraviolet stabilizer. In one example, the reactive ultraviolet stabilizer may be an acrylic monomer represented by the following formula (1).

[화학식 1] [Chemical Formula 1]

Figure pat00001
Figure pat00001

화학식 1에 있어서, R1은 수소 또는 메틸기이고, X는 단일 결합 또는 탄소수 1 내지 5 또는 탄소수 1 내지 3의 알킬렌기이며, R2는 방향족기로 치환된 페닐기, 방향족기로 치환된 히드록시페닐기, 헤테로방향족기로 치환된 페닐기 또는 헤테로방향족기로 치환된 히드록시페닐기이고, 하나의 구체적인 예시에서 R2는 벤조트리아졸기로 치환된 히드록시페닐기일 수 있다. 상기와 같은 반응형 자외선 안정제를 채택함으로써, 우수한 내황변성과 우수한 박리력을 확보할 수 있다.Wherein R 1 is hydrogen or a methyl group, X is a single bond or an alkylene group having 1 to 5 carbon atoms or 1 to 3 carbon atoms, R 2 is a phenyl group substituted with an aromatic group, a hydroxyphenyl group substituted with an aromatic group, A phenyl group substituted with an aromatic group or a hydroxyphenyl group substituted with a heteroaromatic group, and in one specific example, R 2 may be a hydroxyphenyl group substituted with a benzotriazole group. By adopting the reaction type UV stabilizer as described above, excellent yellowing resistance and excellent peeling force can be secured.

자외선 안정제는 (메트)아크릴레이트 100 중량부 대비 1 내지 10 중량부 또는 3 내지 8 중량부일 수 있다. 상기 범위를 만족하는 점착제 조성물로 제조한 봉지재 시트는, 우수한 광학적 특성 및 기계적 특성을 확보할 수 있다.The ultraviolet stabilizer may be 1 to 10 parts by weight or 3 to 8 parts by weight based on 100 parts by weight of (meth) acrylate. The encapsulating material sheet produced from the pressure-sensitive adhesive composition satisfying the above range can ensure excellent optical properties and mechanical properties.

본 출원의 점착제 조성물은 파장변환물질을 포함한다. 예를 들어, 파장변환물질은 유기 안료일 수 있다. 본 출원의 유기 안료는 300nm 내지 600nm, 350nm 내지 550nm 또는 378nm 내지 524nm 파장의 빛을 흡수하여 330nm 내지 620nm, 380nm 내지 570nm 또는 413nm 내지 539nm의 빛을 방출하는 것이면 특별한 제한 없이 사용할 수 있다. 하나의 예시에서, 유기 안료는 나프탈렌계 유기 안료일 수 있으며, 구체적으로는 나프탈렌 1,8:4,5-테트라카르보닉에시드 디이미드(1,8:4,5-tetracarbonic acid diimide), 나프탈렌-1,8-디카르본산 이미드(naphthalene-1,8-dicarbonic acid imide), 4,5-디알콕시나프탈렌-1,8-디카르본산 모노이미드(4,5-dialkoxynaphthalene-1,8-dicarbonic acid monoimide), 4-페녹시나프탈렌-1,8-디카르본산 모노이미드(4-phenoxynaphthalene-1,8-dicarbonic acid monoimide), N-(2-에틸헥실)-4,5-디메톡시나프탈렌-1,8-디카르본산 이미드(N-(2-ethylhexyl)-4,5-dimethoxynaphthalene-1,8-dicarbonic acid imide), N- (2,6-디이소프로필-페닐)-4,5-디메톡시나프탈렌-1,8-디카르본산 이미드(N-(2,6-diisopropyl-phenyl)-4,5-dimethoxynaphthalene-1,8-dicarbonic acid imide), N-(7-트리데실)-4,5-디메톡시-나프탈렌-1,8 디카르본산 이미드(N-(7-tridecyl)-4,5-dimethoxy-naphthalene-1,8 dicarbonic acid imide), N-(2,6-디이소프로필페닐)-4,5-디페녹시나프탈렌-1,8-디카르본산 이미드(N-(2,6-diisopropylphenyl)-4,5-diphenoxynaphthalene-1 ,8-dicarbonic acid imide), 및 N,N'-비스(2,6-디이소프로필페닐)-1,8:4,5-나프탈렌 테트라카르보닉에시드 디이미드(N,N'-bis(2,6-diisopropylphenyl)-1,8:4,5-naphthalene tetracarbonic acid diimide)로 이루어진 군에서 선택된 하나 이상일 수 있으나, 이에 제한되는 것은 아니다. 본 발명의 일 구현예에 있어서, 상기 유기 안료는 BASF사의 Lumogen F Yellow 083, Lumogen F Orange 240, Lumogen F Red 305 및 Lumogen F Violet 570로 이루어진 군에서 선택된 하나 이상일 수 있으나 이에 제한되는 것은 아니다. The pressure-sensitive adhesive composition of the present application comprises a wavelength converting material. For example, the wavelength converting material may be an organic pigment. The organic pigment of the present application can be used without any particular limitation as long as it absorbs light of 300 nm to 600 nm, 350 nm to 550 nm, or 378 nm to 524 nm and emits light of 330 nm to 620 nm, 380 nm to 570 nm, or 413 nm to 539 nm. In one example, the organic pigment may be a naphthalene-based organic pigment, and specifically includes naphthalene 1,8: 4,5-tetracarbonic acid diimide, naphthalene- Naphthalene-1,8-dicarbonic acid imide, 4,5-dialkoxynaphthalene-1,8-dicarbonic acid-1,8-dicarboxylic acid monoimide, acid monoimide, 4-phenoxynaphthalene-1,8-dicarbonic acid monoimide, N- (2-ethylhexyl) -4,5-dimethoxynaphthalene- (2-ethylhexyl) -4,5-dimethoxynaphthalene-1,8-dicarbonic acid imide, N- (2,6-diisopropyl-phenyl) -4,5 (2,6-diisopropyl-phenyl) -4,5-dimethoxynaphthalene-1,8-dicarbonic acid imide), N- (7-tridecyl) imide, (7-tridecyl) -4,5-dimethoxy-naphthalene-1,8 dicarbonic acid imide), N- ( 2,6-diisopropylphenyl) -4,5-diphenoxynaphthalene-1,8-dicarboxylic acid imide (N- (2,6-diisopropylphenyl) -4,5-diphenoxynaphthalene-1,8-dicarbonic acid imide, and N, N'-bis (2,6-diisopropylphenyl) -1,8: 4,5-naphthalenetetracarboxylic acid diimide ) -1,8: 4,5-naphthalene tetracarbonic acid diimide), but the present invention is not limited thereto. In one embodiment of the present invention, the organic pigment may be at least one selected from the group consisting of Lumogen F Yellow 083, Lumogen F Orange 240, Lumogen F Red 305 and Lumogen F Violet 570 from BASF.

상기 파장변환물질은 점착성 중합체 100 중량부에 대하여 0.2 내지 0.8 중량부 또는 0.3 내지 0.7 중량부일 수 있다. 상기 범위를 만족하는 점착제 조성물로 제조한 봉지층은 우수한 기계적 특성 및 광학적 특성을 나타낸다.The wavelength conversion material may be 0.2 to 0.8 parts by weight or 0.3 to 0.7 parts by weight based on 100 parts by weight of the adhesive polymer. The sealing layer made of the pressure sensitive adhesive composition satisfying the above range exhibits excellent mechanical and optical properties.

하나의 예시에 있어서, 본 출원의 점착제 조성물은 할스계 라디칼 스캐빈저를 추가로 포함할 수 있다. 상기 할스계 라디칼 스캐빈저는 하나의 예시에 있어서 NOR-HALS일 수 있다. 점착제 조성물이 할스계 라디칼 스캐빈저를 추가로 포함함으로써, 본 출원의 점착제 조성물로 제조한 봉지층은 고온 고습 조건에 노출되어도 우수한 광학적 특성을 유지할 수 있다.In one example, the pressure-sensitive adhesive composition of the present application may further comprise a horseradish radical scavenger. The Halscad radical scavenger may be NOR-HALS in one example. By further including the horseshoe radial scavenger in the pressure-sensitive adhesive composition, the sealing layer produced from the pressure-sensitive adhesive composition of the present application can maintain excellent optical characteristics even when exposed to high temperature and high humidity conditions.

상기 할스계 라디칼 스캐빈저는 (메트)아크릴레이트 100 중량부 대비 1 내지 5 중량부 또는 1 내지 3 중량부로 포함될 수 있다. 상기 범위에 해당하는 점착제 조성물로 제조한 봉지재 시트는, 우수한 박리력과 우수한 내습열 특성을 확보할 수 있다.The horseradish radical scavenger may be included in an amount of 1 to 5 parts by weight or 1 to 3 parts by weight based on 100 parts by weight of (meth) acrylate. An encapsulating material sheet produced from the pressure-sensitive adhesive composition having the above-mentioned range can secure excellent peel strength and excellent moisture heat resistance.

본 출원은 또한 태양전지용 봉지재 시트에 관한 것이다. 본 출원의 태양전지용 봉지재 시트는 기재; 및 전술한 점착제 조성물의 경화물을 포함하는 봉지층을 포함한다.The present application also relates to an encapsulant sheet for a solar cell. The sealing sheet for a solar cell according to the present application comprises: a substrate; And an encapsulating layer comprising a cured product of the above-described pressure-sensitive adhesive composition.

본 출원의 봉지재 시트의 기재는 고분자 필름일 수 있으며, 예를 들어 폴리에틸렌(PE), 폴리프로필렌(PP), 폴리에틸렌테레프탈레이트(PET), 폴리페닐렌설파이드(PPS), 폴리에틸렌나프탈레이트(PEN), 폴리비닐플루오라이드(PVF), 폴리비닐리덴플루오라이드(PVDF), 에틸렌테트라플루오르에틸렌(ETFE), 폴리클로로트리플루오로에틸렌(PCTFE), 에틸렌클로로트리플루오로에틸렌(ECTFE)로 이루어진 군에서 선택한 어느 하나이다.The base material of the encapsulating material sheet of the present application may be a polymer film. Examples of the base material include polyethylene (PE), polypropylene (PP), polyethylene terephthalate (PET), polyphenylene sulfide (PPS), polyethylene naphthalate Selected from the group consisting of polyvinyl fluoride (PVF), polyvinylidene fluoride (PVDF), ethylene tetrafluoroethylene (ETFE), polychlorotrifluoroethylene (PCTFE), ethylene chlorotrifluoroethylene (ECTFE) It is either.

본 출원의 태양전지용 봉지재 시트에 있어서, 점착제 조성물에 관한 구체적인 내용은 전술한 점착제 조성물에 관한 부분에서 설명한 바와 동일하므로, 생략하기로 한다.In the sealing sheet for a solar cell according to the present application, the specific content of the pressure-sensitive adhesive composition is the same as that described in the above-mentioned portion relating to the pressure-sensitive adhesive composition, and therefore will be omitted.

본 출원의 점착제 조성물로 제조한 봉지층은 전면 부재에 대한 박리력(ASTM D903)이 800gf/in 내지 1200gf/in 또는 900gf/in 내지 1100gf/in 이다.The sealing layer made of the pressure-sensitive adhesive composition of the present application has a peel force (ASTM D903) of 800 gf / in to 1200 gf / in or 900 gf / in to 1100 gf / in on the front member.

본 출원은 또한 본 출원의 봉지재 시트를 포함하는 태양전지 모듈에 관한 것이다. 본 출원의 태양전지 모듈에 있어서, 봉지재 시트에 관한 구체적인 내용은 전술한 봉지재 시트에 관한 부분에서 설명한 바와 동일하므로, 생략하기로 한다.The present application also relates to a solar cell module comprising an encapsulation sheet of the present application. In the solar cell module of the present application, the details of the encapsulation material sheet are the same as those described above in connection with the encapsulation material sheet, and therefore will not be described.

본 출원에 따른 점착제 조성물은 조성물 자체를 도포하여 수 분 내에 열 경화를 진행해 가교밀도를 향상시킬 수 있어 롤 투 롤(Roll to Roll) 연속 공정이 가능하다. 따라서, 생산속도 및 생산효율이 향상된다. 또한, 본 출원에 따른 점착제 조성물은 파장변환 안료를 포함하여 우수한 기계적 특성과 내습열 특성을 확보하였다.The pressure-sensitive adhesive composition according to the present invention can improve the crosslinking density by applying the composition itself and proceeding thermosetting within a few minutes, thus enabling a roll-to-roll continuous process. Thus, production speed and production efficiency are improved. In addition, the pressure-sensitive adhesive composition according to the present application has excellent mechanical properties and anti-wet heat characteristics, including wavelength conversion pigments.

도 1은 본 출원의 구현예에 따른 태양전지 모듈을 예시적으로 보여주는 도면이다.
도 2는 본 출원의 실시예에 따라 제조된 적층체를 간략히 보여주는 도면이다.
FIG. 1 is a view illustrating an exemplary solar cell module according to an embodiment of the present application.
Figure 2 is a simplified view of a laminate made according to an embodiment of the present application.

이하, 본 발명을 실험예에 의해 보다 자세하게 설명하지만, 아래의 실시예는 본 발명을 단지 상세하게 설명하기 위한 것이며 본 발명의 범주를 한정하기 위한 것은 아니다.Hereinafter, the present invention will be described in more detail by way of Experimental Examples, but the following Examples are for explaining the present invention only in detail and are not intended to limit the scope of the present invention.

도 2와 같이 유리(210), 봉지층(220) 및 기재(230)로 이루어진 적층체(200)를 제조하였다. 적층체를 제조하는데 있어서, 점착제 조성물이 포함하는 파장변환 안료의 함량에 따른 기계적 특성 및 광학적 특성과, 할스계 라디칼 스캐빈저의 포함 여부에 따른 기계적 특성 및 광학적 특성을 측정하였다.A laminate 200 made of glass 210, an encapsulating layer 220 and a substrate 230 was prepared as shown in Fig. Mechanical properties and optical properties of the pressure sensitive adhesive composition were measured according to the contents of the wavelength conversion pigments contained in the pressure - sensitive adhesive composition and the inclusion of a horseradish radical scavenger.

실험예Experimental Example 1  One

내부에 질소가스가 환류되고, 온도 조절이 용이하도록 냉각 장치를 설치한 1L 반응기에 2-에틸헥실 아크릴레이트(EHA) 50 중량부(142.9g), 메틸 아크릴레이트(MA) 40 중량부(114.3g), 2-히드록시에틸 아크릴레이트(HEA) 10 중량부(28.6g) 및 오츠카 케미컬사의 반응형 자외선 흡수제인 RUVA-93을 5 중량부(14.3g) 투입하였다. 이어서, 에틸아세테이트(EAc) 700g을 용제로 투입하고, 산소 제거를 위하여 질소 가스를 60분 동안 퍼징(purging)한 후, 온도를 60℃로 유지한 상태에서 반응 개시제인 V-65(2,2'-azobis(2,4-dimethyl valeronitrile))를 1400ppm(0.42g) 투입하여 반응을 개시시켰다. 이후, 약 5시간 반응을 시켜 점착성 중합체(EMH-R)를 제조하였다. 또한, 샘플에 따라 추가적으로 상기 점착성 중합체를 포함하는 조성물에 BASF사의 파장변환 안료인 Lumogen F Violet 570을 추가적으로 포함시켜 하기 표 1과 같은 점착층을 형성할 수 있는 점착제 조성물 샘플을 제조하였다.50 parts by weight of 2-ethylhexyl acrylate (EHA) (142.9 g) and 40 parts by weight of methyl acrylate (MA) (114.3 g) were added to a 1 L reactor equipped with a cooling device ), 10 parts by weight (28.6 g) of 2-hydroxyethyl acrylate (HEA) and 5 parts by weight (14.3 g) of RUVA-93 as a reactive ultraviolet absorbent of Otsuka Chemical Co. were added. Subsequently, 700 g of ethyl acetate (EAc) was poured into the solvent, nitrogen gas was purged for 60 minutes to remove oxygen, and the reaction initiator V-65 (2,2 '-azobis (2,4-dimethyl valeronitrile)) at 1400 ppm (0.42 g). Thereafter, the reaction was conducted for about 5 hours to prepare a sticky polymer (EMH-R). Further, according to the sample, a composition containing the above adhesive polymer was further added to Lumogen F Violet 570, a wavelength conversion pigment of BASF, to prepare a pressure-sensitive adhesive composition sample capable of forming the pressure-sensitive adhesive layer as shown in Table 1 below.

상기 점착제의 고형분 함량은 26.24%이다. 상기 점착제에 메틸에틸케톤(MEK)를 첨가하여 고형분 함량이 25%가 되도록 한 후, 미츠이 케미컬사의 TAKENATE D-110N 이소시아네이트 가교제를 0.125% 첨가한 점착제 조성물을 제조하였다. TOYOBO 사의 A4200 PET 일면에 상기 점착제 조성물을 두께가 약 30μm정도가 되도록 코팅한 후, 120℃에서 2분간 건조하여 점착제 층을 형성하였다. 그 위에 SKC Haas사의 Rf-02N 이형 PET를 사용해 덮은 후, 40℃ 오븐에 48시간동안 에이징(aging)하였다. 그 후 유리 위에 이형 처리된 PET 필름을 박리하여 적층체를 제조해 샘플을 얻었다.The solid content of the pressure-sensitive adhesive is 26.24%. Methyl ethyl ketone (MEK) was added to the pressure-sensitive adhesive so that the solid content became 25%, and 0.125% of TAKENATE D-110N isocyanate crosslinking agent of Mitsui Chemical Co. was added to prepare a pressure-sensitive adhesive composition. The pressure-sensitive adhesive composition was coated on one side of A4200 PET manufactured by TOYOBO Co., Ltd. to a thickness of about 30 mu m and dried at 120 DEG C for 2 minutes to form a pressure-sensitive adhesive layer. Covered with Rf-02N type PET of SKC Haas, and then aged in a 40 ° C oven for 48 hours. Thereafter, the release-treated PET film was peeled off from the glass to produce a laminate to obtain a sample.

Figure pat00002
Figure pat00002

상기 표 1을 통해, 파장변환 안료가 특정한 범위를 벗어나 점착제 조성물에 포함될 경우 박리력이 현저하게 감소하는 것을 알 수 있다.It can be seen from Table 1 that the peeling force is remarkably reduced when the wavelength converting pigment is included in the pressure sensitive adhesive composition beyond a specific range.

상기 표 1에 기재된 점착제를 이용해 제조한 적층체들을 85℃, 85% 상대습도에서 2000시간 동안 방치하는 내습열 테스트(85℃, 85% RH 2000hr 테스트)를 실시하였으며, 자외선을 2000시간 동안 조사하는 기폭 테스트(Q-UVB 테스트)를 실시하였다. 그 결과는 하기 표 2와 같다.(85 ° C, 85% RH, 2000 hr test) in which the laminate prepared by using the pressure-sensitive adhesive described in Table 1 was allowed to stand at 85 ° C. and 85% relative humidity for 2000 hours. Ultraviolet rays were irradiated for 2000 hours And an explosion test (Q-UVB test). The results are shown in Table 2 below.

Figure pat00003
Figure pat00003

상기 표 2를 통해, 자외선 안정제와 파장변환 안료가 포함되지 않은 점착제 조성물(EMH(refer.))의 경우, 테스트 결과 광학적 특성이 테스트 전보다 현저하게 악화되는 것을 알 수 있었다. 또한, 자외선 안정제만을 포함하거나, 자외선 안정제와 함께 파장변환 안료를 특정한 함량으로 포함하는 점착제 조성물의 경우, 테스트 후에도 초기의 광학적 특성이 비교적 양호하게 유지되는 것을 알 수 있다.From the above Table 2, it was found that, in the case of the pressure-sensitive adhesive composition (EMH (refer.)) Not containing the ultraviolet stabilizer and the wavelength conversion pigment, the test results showed that the optical properties were significantly worse than before the test. In addition, in the case of the pressure-sensitive adhesive composition containing only the ultraviolet light stabilizer or containing the wavelength conversion pigment in a specific amount together with the ultraviolet light stabilizer, it can be seen that the initial optical properties remain relatively good even after the test.

실험예Experimental Example 2 2

내부에 질소가스가 환류되고, 온도 조절이 용이하도록 냉각 장치를 설치한 1L 반응기에 2-에틸헥실 아크릴레이트(EHA) 50 중량부(142.9g), 메틸 아크릴레이트(MA) 40 중량부(114.3g), 2-히드록시에틸 아크릴레이트(HEA) 10 중량부(28.6g), 오츠카 케미컬사의 반응형 자외선 흡수제인 RUVA-93을 5 중량부(14.3g) 및 할스계 라디칼 스캐빈저인 NOR-HALS 2 중량부(5.72g)를 투입하였다. 이어서, 에틸아세테이트(EAc) 700g을 용제로 투입하고, 산소 제거를 위하여 질소 가스를 60분 동안 퍼징(purging)한 후, 온도를 60℃로 유지한 상태에서 반응 개시제인 V-65(2,2'-azobis(2,4-dimethyl valeronitrile))를 1400ppm(0.42g) 투입하여 반응을 개시시켰다. 이후, 약 5시간 반응을 시켜 점착성 중합체(EMH-RH)를 제조하였다. 또한, 샘플에 따라 추가적으로 BASF사의 파장변환 안료인 Lumogen F Violet 570, BASF사의 할스계 라디칼 스케빈저인 Tinuvin123을 포함시켜 하기 표 3과 같은 점착제 샘플을 제조하였다.50 parts by weight of 2-ethylhexyl acrylate (EHA) (142.9 g) and 40 parts by weight of methyl acrylate (MA) (114.3 g) were added to a 1 L reactor equipped with a cooling device ), 10 parts by weight (28.6 g) of 2-hydroxyethyl acrylate (HEA), 5 parts by weight (14.3 g) of RUVA-93 as a reactive ultraviolet absorbent of Otsuka Chemical Co. and NOR-HALS 2 parts by weight (5.72 g) was added thereto. Subsequently, 700 g of ethyl acetate (EAc) was poured into the solvent, nitrogen gas was purged for 60 minutes to remove oxygen, and the reaction initiator V-65 (2,2 '-azobis (2,4-dimethyl valeronitrile)) at 1400 ppm (0.42 g). Thereafter, the reaction was carried out for about 5 hours to prepare a sticky polymer (EMH-RH). Lumogen F Violet 570, a wavelength-converting pigment of BASF, and Tinuvin 123, a Halss radical scavenger of BASF, were also added according to the samples to prepare pressure sensitive adhesive samples as shown in Table 3 below.

상기 점착제의 고형분 함량은 23.43%이다. 상기 점착제에 메틸에틸케톤(MEK)를 첨가하여 고형분 함량이 20%가 되도록 한 후, 미츠이 케미컬사의 TAKENATE D-110N 이소시아네이트 가교제를 0.125% 첨가한 점착제 조성물을 제조하였다. TOYOBO 사의 A4200 PET 일면에 상기 점착제 조성물을 두께가 약 30μm정도가 되도록 코팅한 후, 120℃에서 2분간 건조하여 점착제 층을 형성하였다. 그 위에 SKC Haas사의 Rf-02N 이형 PET를 사용해 덮은 후, 40℃ 오븐에 48시간동안 에이징(aging)하였다. 그 후 유리 위에 이형 처리된 PET 필름을 박리하여 적층체를 제조해 샘플을 얻었다.The solid content of the pressure-sensitive adhesive is 23.43%. Methyl ethyl ketone (MEK) was added to the pressure-sensitive adhesive so as to have a solid content of 20%, and 0.125% of TAKENATE D-110N isocyanate crosslinking agent of Mitsui Chemical Co. was added to prepare a pressure-sensitive adhesive composition. The pressure-sensitive adhesive composition was coated on one side of A4200 PET manufactured by TOYOBO Co., Ltd. to a thickness of about 30 mu m and dried at 120 DEG C for 2 minutes to form a pressure-sensitive adhesive layer. Covered with Rf-02N type PET of SKC Haas, and then aged in a 40 ° C oven for 48 hours. Thereafter, the release-treated PET film was peeled off from the glass to produce a laminate to obtain a sample.

Figure pat00004
Figure pat00004

상기 표 3을 통해, 할스계 라디칼 스캐빈져의 종류에 따라 점착제 조성물로 제조한 봉지층의 박리력이 현저히 감소할 수 있다는 것을 알 수 있다.From Table 3, it can be seen that the peel strength of the seal layer made of the pressure-sensitive adhesive composition can be remarkably reduced depending on the kind of the Halss radical scavenger.

Figure pat00005
Figure pat00005

상기 표 4를 통해, NOR-HALS를 포함하는 점착제 조성물로 제조한 봉지층의 경우, 내습열 테스트와 기폭 테스트에서 우수한 광학적 특성을 유지하는 것을 확인할 수 있다.From Table 4, it is confirmed that the sealing layer made of the pressure-sensitive adhesive composition containing NOR-HALS maintains excellent optical characteristics in the anti-wet heat test and the ignition test.

100: 태양전지 모듈
110: 기재층
120: 봉지재층
130: 전면 부재
140: 태양전지셀
200: 적층체
210: 유리
220: 봉지재층
230: 기재
100: solar cell module
110: substrate layer
120: encapsulant layer
130: front member
140: Solar cell
200: laminate
210: glass
220: encapsulant layer
230: substrate

Claims (12)

(메트)아크릴레이트와 반응형 자외선 안정제의 공중합체를 포함하는 점착성 중합체; 및 상기 점착성 중합체 100 중량부에 대하여 0.2 내지 0.8 중량부의 파장변환물질을 포함하는 점착제 조성물.A tacky polymer comprising a copolymer of (meth) acrylate and a reactive ultraviolet stabilizer; And 0.2 to 0.8 parts by weight of a wavelength converting material based on 100 parts by weight of the pressure-sensitive adhesive polymer. 제 1항에 있어서,
(메트)아크릴레이트는 가교성 관능기를 포함하는 (메트)아크릴레이트 및 알킬(메트)아크릴레이트를 포함하는 점착제 조성물.
The method according to claim 1,
(Meth) acrylate comprises a (meth) acrylate and an alkyl (meth) acrylate containing a crosslinkable functional group.
제 2항에 있어서,
가교성 관능기를 포함하는 (메트)아크릴레이트는 전체 (메트)아크릴레이트 100 중량부에 대하여 3 내지 30 중량부인 점착제 조성물.
3. The method of claim 2,
Wherein the (meth) acrylate containing a crosslinkable functional group is 3 to 30 parts by weight based on 100 parts by weight of the total (meth) acrylate.
제 1항에 있어서,
자외선 안정제는 하기 화학식 1로 나타내어지는 아크릴계 단량체인 점착제 조성물:
[화학식 1]
Figure pat00006

화학식 1에 있어서, R1은 수소 또는 메틸기이고, X는 단일 결합 또는 탄소수 1 내지 5의 알킬렌기이며, R2는 방향족기로 치환된 페닐기, 방향족기로 치환된 히드록시페닐기, 헤테로방향족기로 치환된 페닐기 또는 헤테로방향족기로 치환된 히드록시페닐기이다.
The method according to claim 1,
Wherein the ultraviolet light stabilizer is an acrylic monomer represented by the following formula (1):
[Chemical Formula 1]
Figure pat00006

Wherein R 1 is hydrogen or a methyl group, X is a single bond or an alkylene group having 1 to 5 carbon atoms, R 2 is a phenyl group substituted with an aromatic group, a hydroxyphenyl group substituted with an aromatic group, a phenyl group substituted with a heteroaromatic group Or a hydroxyphenyl group substituted with a heteroaromatic group.
제 1항에 있어서,
자외선 안정제의 함량은 (메트)아크릴레이트 100 중량부 대비 1 내지 10 중량부인 점착제 조성물.
The method according to claim 1,
Wherein the content of the ultraviolet light stabilizer is 1 to 10 parts by weight based on 100 parts by weight of the (meth) acrylate.
제 1항에 있어서,
파장변환물질은 유기 안료인 점착제 조성물.
The method according to claim 1,
Wherein the wavelength conversion material is an organic pigment.
제 6항에 있어서,
파장변환 물질은 300nm 내지 600nm의 빛을 흡수하여 330nm 내지 620nm의 빛을 방출하는 유기 안료인 점착제 조성물.
The method according to claim 6,
Wherein the wavelength converting material is an organic pigment that absorbs light of 300 to 600 nm and emits light of 330 to 620 nm.
제 6항에 있어서,
파장변환 물질은 나프탈렌계 유기 안료인 점착제 조성물.
The method according to claim 6,
Wherein the wavelength conversion material is a naphthalene-based organic pigment.
제 1항에 있어서,
점착성 중합체는 할스계 라디칼 스캐빈저를 추가로 포함하는 점착제 조성물.
The method according to claim 1,
Wherein the tacky polymer further comprises a horseradish radical scavenger.
제 9항에 있어서,
라디칼 스캐빈저의 함량은 (메타)아크릴레이트 100 중량부 대비 1 내지 5 중량부인 점착제 조성물.
10. The method of claim 9,
Wherein the content of the radical scavenger is 1 to 5 parts by weight relative to 100 parts by weight of (meth) acrylate.
기재; 및
제 1항의 점착제 조성물의 경화물을 포함하는 봉지층을 포함하고,
상기 봉지층의 박리력(ASTM D903)이 800gf/in 내지 1200gf/in인 태양전지용 봉지재 시트.
materials; And
A pressure-sensitive adhesive composition comprising a sealing layer comprising a cured product of the pressure-sensitive adhesive composition of claim 1,
Wherein the sealing layer has a peeling force (ASTM D903) of 800 gf / in to 1200 gf / in.
제 11항의 봉지재 시트를 포함하는 태양전지 모듈.A solar cell module comprising the encapsulating material sheet of claim 11.
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