JP5891836B2 - Sealant for solar cell module - Google Patents
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- JP5891836B2 JP5891836B2 JP2012033911A JP2012033911A JP5891836B2 JP 5891836 B2 JP5891836 B2 JP 5891836B2 JP 2012033911 A JP2012033911 A JP 2012033911A JP 2012033911 A JP2012033911 A JP 2012033911A JP 5891836 B2 JP5891836 B2 JP 5891836B2
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- 239000000565 sealant Substances 0.000 title 1
- 150000001451 organic peroxides Chemical class 0.000 claims description 49
- 239000005038 ethylene vinyl acetate Substances 0.000 claims description 37
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 claims description 37
- 239000003566 sealing material Substances 0.000 claims description 35
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 claims description 8
- 238000004132 cross linking Methods 0.000 description 21
- 238000005187 foaming Methods 0.000 description 13
- 230000000052 comparative effect Effects 0.000 description 9
- 150000001875 compounds Chemical class 0.000 description 9
- 238000010438 heat treatment Methods 0.000 description 7
- 238000010248 power generation Methods 0.000 description 6
- 239000011521 glass Substances 0.000 description 5
- 230000008961 swelling Effects 0.000 description 5
- -1 t-amyl- (2-ethylhexyl) Chemical group 0.000 description 5
- 239000000654 additive Substances 0.000 description 4
- 238000002156 mixing Methods 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 238000007789 sealing Methods 0.000 description 4
- 229910021417 amorphous silicon Inorganic materials 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 239000007822 coupling agent Substances 0.000 description 3
- 229910021419 crystalline silicon Inorganic materials 0.000 description 3
- 238000000354 decomposition reaction Methods 0.000 description 3
- 239000008393 encapsulating agent Substances 0.000 description 3
- 239000004611 light stabiliser Substances 0.000 description 3
- 238000005259 measurement Methods 0.000 description 3
- 239000004065 semiconductor Substances 0.000 description 3
- 239000003381 stabilizer Substances 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- KUDUQBURMYMBIJ-UHFFFAOYSA-N 2-prop-2-enoyloxyethyl prop-2-enoate Chemical compound C=CC(=O)OCCOC(=O)C=C KUDUQBURMYMBIJ-UHFFFAOYSA-N 0.000 description 2
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- KTSFMFGEAAANTF-UHFFFAOYSA-N [Cu].[Se].[Se].[In] Chemical compound [Cu].[Se].[Se].[In] KTSFMFGEAAANTF-UHFFFAOYSA-N 0.000 description 2
- 239000003963 antioxidant agent Substances 0.000 description 2
- 238000007664 blowing Methods 0.000 description 2
- 239000003086 colorant Substances 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 238000000465 moulding Methods 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- 229910021420 polycrystalline silicon Inorganic materials 0.000 description 2
- 238000005979 thermal decomposition reaction Methods 0.000 description 2
- 238000010792 warming Methods 0.000 description 2
- 239000008096 xylene Substances 0.000 description 2
- YWHMJMBYBJBHKE-UHFFFAOYSA-N (4-ethyl-2,2-dimethyloctan-3-yl) hydroxy carbonate Chemical compound CCCCC(CC)C(C(C)(C)C)OC(=O)OO YWHMJMBYBJBHKE-UHFFFAOYSA-N 0.000 description 1
- KOMNUTZXSVSERR-UHFFFAOYSA-N 1,3,5-tris(prop-2-enyl)-1,3,5-triazinane-2,4,6-trione Chemical compound C=CCN1C(=O)N(CC=C)C(=O)N(CC=C)C1=O KOMNUTZXSVSERR-UHFFFAOYSA-N 0.000 description 1
- BWOITHKYQUJGSB-UHFFFAOYSA-N 2-methylbutan-2-ylperoxycyclohexane Chemical compound CCC(C)(C)OOC1CCCCC1 BWOITHKYQUJGSB-UHFFFAOYSA-N 0.000 description 1
- POZWNWYYFQVPGC-UHFFFAOYSA-N 3-methoxysilylpropyl 2-methylprop-2-enoate Chemical compound CO[SiH2]CCCOC(=O)C(C)=C POZWNWYYFQVPGC-UHFFFAOYSA-N 0.000 description 1
- DBCAQXHNJOFNGC-UHFFFAOYSA-N 4-bromo-1,1,1-trifluorobutane Chemical compound FC(F)(F)CCCBr DBCAQXHNJOFNGC-UHFFFAOYSA-N 0.000 description 1
- 229940126062 Compound A Drugs 0.000 description 1
- 239000004641 Diallyl-phthalate Substances 0.000 description 1
- NLDMNSXOCDLTTB-UHFFFAOYSA-N Heterophylliin A Natural products O1C2COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC2C(OC(=O)C=2C=C(O)C(O)=C(O)C=2)C(O)C1OC(=O)C1=CC(O)=C(O)C(O)=C1 NLDMNSXOCDLTTB-UHFFFAOYSA-N 0.000 description 1
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- NOZAQBYNLKNDRT-UHFFFAOYSA-N [diacetyloxy(ethenyl)silyl] acetate Chemical compound CC(=O)O[Si](OC(C)=O)(OC(C)=O)C=C NOZAQBYNLKNDRT-UHFFFAOYSA-N 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 125000003668 acetyloxy group Chemical group [H]C([H])([H])C(=O)O[*] 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 239000002671 adjuvant Substances 0.000 description 1
- 125000002723 alicyclic group Chemical group 0.000 description 1
- 125000003545 alkoxy group Chemical group 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 description 1
- 239000012965 benzophenone Substances 0.000 description 1
- QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical compound C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 description 1
- 239000012964 benzotriazole Substances 0.000 description 1
- ZPOLOEWJWXZUSP-AATRIKPKSA-N bis(prop-2-enyl) (e)-but-2-enedioate Chemical compound C=CCOC(=O)\C=C\C(=O)OCC=C ZPOLOEWJWXZUSP-AATRIKPKSA-N 0.000 description 1
- ZPOLOEWJWXZUSP-WAYWQWQTSA-N bis(prop-2-enyl) (z)-but-2-enedioate Chemical compound C=CCOC(=O)\C=C/C(=O)OCC=C ZPOLOEWJWXZUSP-WAYWQWQTSA-N 0.000 description 1
- QUDWYFHPNIMBFC-UHFFFAOYSA-N bis(prop-2-enyl) benzene-1,2-dicarboxylate Chemical compound C=CCOC(=O)C1=CC=CC=C1C(=O)OCC=C QUDWYFHPNIMBFC-UHFFFAOYSA-N 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- XLJMAIOERFSOGZ-UHFFFAOYSA-M cyanate Chemical compound [O-]C#N XLJMAIOERFSOGZ-UHFFFAOYSA-M 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 125000003700 epoxy group Chemical group 0.000 description 1
- FWDBOZPQNFPOLF-UHFFFAOYSA-N ethenyl(triethoxy)silane Chemical compound CCO[Si](OCC)(OCC)C=C FWDBOZPQNFPOLF-UHFFFAOYSA-N 0.000 description 1
- WOXXJEVNDJOOLV-UHFFFAOYSA-N ethenyl-tris(2-methoxyethoxy)silane Chemical compound COCCO[Si](OCCOC)(OCCOC)C=C WOXXJEVNDJOOLV-UHFFFAOYSA-N 0.000 description 1
- STVZJERGLQHEKB-UHFFFAOYSA-N ethylene glycol dimethacrylate Substances CC(=C)C(=O)OCCOC(=O)C(C)=C STVZJERGLQHEKB-UHFFFAOYSA-N 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 239000002803 fossil fuel Substances 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 125000000962 organic group Chemical group 0.000 description 1
- 150000003961 organosilicon compounds Chemical class 0.000 description 1
- 238000005502 peroxidation Methods 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 229920002037 poly(vinyl butyral) polymer Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 230000002285 radioactive effect Effects 0.000 description 1
- 238000012827 research and development Methods 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 238000005096 rolling process Methods 0.000 description 1
- 150000003377 silicon compounds Chemical class 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 230000004083 survival effect Effects 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
- 150000003609 titanium compounds Chemical class 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- 238000002834 transmittance Methods 0.000 description 1
- 239000006097 ultraviolet radiation absorber Substances 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
Images
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- Y—GENERAL 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
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E10/00—Energy generation through renewable energy sources
- Y02E10/50—Photovoltaic [PV] energy
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- Photovoltaic Devices (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Description
本発明は、太陽電池モジュール用封止材に関する。 The present invention relates to a solar cell module sealing material.
近年、地球温暖化対策や化石燃料に代わる代替エネルギーの利用など、各種分野において環境問題に対する意識が高まっている。例えば発電分野においては、原子力発電は放射能汚染の危険性が常につきまとい、石油を使用する火力発電ではCO2排出に伴う地球温暖化の問題がある。そこで、このような問題のないクリーンエネルギーとして太陽光発電が注目されており、実用化も確実に進められている。太陽光発電に利用される太陽電池モジュールには種々の形態があり、代表的なものとしては、結晶シリコン太陽電池、多結晶シリコン太陽電池、アモルファスシリコン太陽電池、銅インジウムセレナイド太陽電池、及び化合物半導体太陽電池等が挙げられる。中でも、結晶シリコン太陽電池、化合物半導体太陽電池、及びアモルファスシリコン太陽電池は、比較的低コストで大面積化が可能なため、最近ではこれらの太陽電池について活発に研究開発が進められている。 In recent years, awareness of environmental issues has increased in various fields, such as countermeasures against global warming and the use of alternative energy instead of fossil fuels. For example, in the power generation field, nuclear power generation always has a risk of radioactive contamination, and thermal power generation using oil has a problem of global warming due to CO 2 emission. Therefore, photovoltaic power generation is attracting attention as clean energy free of such problems, and its practical application is being promoted with certainty. There are various types of solar cell modules used for photovoltaic power generation. Typical examples include crystalline silicon solar cells, polycrystalline silicon solar cells, amorphous silicon solar cells, copper indium selenide solar cells, and compounds. A semiconductor solar cell etc. are mentioned. Among these, crystalline silicon solar cells, compound semiconductor solar cells, and amorphous silicon solar cells can be increased in area at a relatively low cost, and recently research and development of these solar cells has been actively conducted.
これら各種太陽電池モジュールの基本的構成は、図1に示すように、複数の太陽電池用セル(太陽電池素子)101が、表面(光入射側)保護用のガラス板102と耐候性を有するバックシート103とによって挟持され、ガラス板102とバックシート103との間には、これらを接着し、太陽電池用セル101を封止するためのEVAやポリビニルブチラールなどの熱可塑性透明樹脂から成る封止材104が介装されている。
As shown in FIG. 1, the basic configuration of these various solar cell modules is that a plurality of solar cell cells (solar cell elements) 101 have a weather resistance and a
ところで、太陽電池モジュールに用いられる封止材には、耐候性、接着性、耐熱性などの物性が要求される。そこで、これらの物性を担保するため、従来からEVAを有機過酸化物によって架橋している。 By the way, the sealing material used in the solar cell module is required to have physical properties such as weather resistance, adhesiveness, and heat resistance. Therefore, in order to ensure these physical properties, EVA is conventionally crosslinked with an organic peroxide.
EVAに加えられた有機過酸化物により分解してEVAを架橋させると、架橋度の指標となるゲル分率が向上する。EVAのゲル分率を向上することにより太陽電池用封止材の耐熱性及び強度を向上することができ、屋外等の環境下で使用される太陽電池にはゲル分率が80%以上であるEVAが必要である。したがって、屋外等で使用される太陽電池を提供するためには、有機過酸化物をEVA中に含有させてEVAを架橋することが必要となっている。 When EVA is crosslinked by being decomposed by the organic peroxide added to EVA, the gel fraction serving as an index of the degree of crosslinking is improved. By improving the gel fraction of EVA, the heat resistance and strength of the solar cell encapsulant can be improved, and the gel fraction is 80% or more for solar cells used outdoors. EVA is required. Therefore, in order to provide a solar cell used outdoors or the like, it is necessary to include EVA in the EVA to crosslink the EVA.
したがって、有機過酸化物による架橋においては、加熱により有機過酸化物を分解させる工程が必要となる。そのため、有機過酸化物の中でも1時間半減期温度が130〜160℃であるジアルキルパーオキサイド型のものを用いた場合、分解及び架橋反応をするための時間を要するために、封止工程における生産性が低いという問題があった。なお、半減期温度とは有機過酸化物の半分が分解する温度のことである。 Therefore, in the crosslinking with the organic peroxide, a step for decomposing the organic peroxide by heating is required. Therefore, in the case of using a dialkyl peroxide type organic peroxide having a one-hour half-life temperature of 130 to 160 ° C., it takes time to perform decomposition and crosslinking reaction. There was a problem of low nature. The half-life temperature is a temperature at which half of the organic peroxide is decomposed.
しかしながら、半減期温度が100〜130℃と低いパーオキシエステル型やパーオキシケタール型のような有機過酸化物を使用すると、短時間での架橋が可能になるものの、封止材に有機過酸化物の分解物に起因すると思われる発泡(膨れ)現象が起こる問題が生じる。発泡は、EVA封止材の密着性を低下させる要因となり、封止性能が低下、太陽電池の寿命と発電効率が低下するという問題が生じる。 However, when organic peroxides such as peroxyester type and peroxyketal type having a low half-life temperature of 100 to 130 ° C. are used, crosslinking in a short time is possible, but organic peroxide is used for the sealing material. There arises a problem that a foaming (swelling) phenomenon which is considered to be caused by a decomposition product of the product occurs. Foaming causes a decrease in the adhesion of the EVA sealing material, resulting in a problem that the sealing performance is lowered and the lifetime and power generation efficiency of the solar cell are lowered.
さらに、半減期温度が低い有機過酸化物を使用した場合、EVAに有機過酸化物を混練させた際にスコーチ(早期架橋)を起こし、作業性を著しく低下させるという問題も生じる。 Further, when an organic peroxide having a low half-life temperature is used, scorching (early crosslinking) occurs when the organic peroxide is kneaded with EVA, and the workability is significantly reduced.
そこで特許文献1には、パーオキシモノカーボネート型やパーオキシケタール型の有機過酸化物100重量部に鎖状または脂環状のハイドロパーオキサイドを4〜50重量部添加することで、スコーチを防止することが可能であることが示されている。しかしながら、スコーチを防止できる反面、耐熱性に必要なゲル分率に達するまでの架橋時間が延長してしまうという問題があった。 Therefore, Patent Document 1 prevents scorch by adding 4 to 50 parts by weight of a chain or alicyclic hydroperoxide to 100 parts by weight of a peroxymonocarbonate type or peroxyketal type organic peroxide. It has been shown that it is possible. However, while scorching can be prevented, there is a problem that the crosslinking time until the gel fraction required for heat resistance is reached is extended.
また、特許文献2には、t−ブチル−(2−エチルヘキシル)パーオキシモノカーボネートにt−アミル−(2−エチルヘキシル)パーオキシモノカーボネートを添加することでスコーチを防止しつつ架橋時間を短縮できることが可能であることが開示されている。しかしながら、耐熱性に必要なゲル分率に達しないという問題があった。 Patent Document 2 describes that the addition of t-amyl- (2-ethylhexyl) peroxymonocarbonate to t-butyl- (2-ethylhexyl) peroxymonocarbonate can shorten the crosslinking time while preventing scorch. Is disclosed to be possible. However, there was a problem that the gel fraction required for heat resistance was not reached.
しかしながら、特許文献1のような有機過酸化物の配合では、確実に発泡(膨れ)を防止できないことが知見された。そこで、本発明者が鋭意検討の結果、ある特定の有機過酸化物のみを配合することによって、太陽電池モジュールにおける膨れを確実に防止できることを知見し、本発明を完成させるに至った。 However, it has been found that foaming (blowing) cannot be reliably prevented by blending an organic peroxide as in Patent Document 1. Therefore, as a result of intensive studies by the present inventors, it has been found that the swelling of the solar cell module can be reliably prevented by blending only a specific organic peroxide, and the present invention has been completed.
すなわち、本発明は上記課題を解決するものであって、その目的とするところは、有機過酸化物に起因する膨れを確実に防止できる、太陽電池モジュール用封止材を提供することにある。 That is, this invention solves the said subject, and the place made into the objective is providing the sealing material for solar cell modules which can prevent the swelling resulting from an organic peroxide reliably.
そのための手段として、本発明は、酢酸ビニルより形成される構造単位を25〜35重量%有するEVAと、有機過酸化物とを含有する太陽電池モジュール用封止材であって、前記有機過酸化物として、下記一般式で示される有機過酸化物(1)と有機過酸化物(2)の重量比が(1)/(2)=100/10〜100/70であることを特徴とする。
このとき、前記有機過酸化物の含有量は、前記EVA100重量部に対して、0.1〜3.0重量部とする。また、EVA中の酢酸ビニルより形成される構造単位は、25〜35重量%であることが好ましい。 At this time, the content of the organic peroxide is 0.1 to 3.0 parts by weight with respect to 100 parts by weight of the EVA. Moreover, it is preferable that the structural unit formed from the vinyl acetate in EVA is 25 to 35 weight%.
なお、本発明において数値範囲を示す「○○〜××」とは、その下限(○○)と上限(××)とを含む概念である。したがって、正確に表せば「○○以上××以下」となる。 In the present invention, “OO to XX” indicating a numerical range is a concept including a lower limit (OO) and an upper limit (XX). Therefore, if it is expressed accurately, it will be “XX or more and XX or less”.
本発明の封止材によれば、EVAに対して特定の有機過酸化物のみを配合していることによって、封止材の良好な耐候性、接着性、耐熱性などを担保しながら、EVAを短時間で架橋できると共に、さらに太陽電池モジュールの各界面における発泡(膨れ)を抑制できる。 According to the sealing material of the present invention, by blending only a specific organic peroxide with EVA, EVA ensures good weather resistance, adhesiveness, heat resistance and the like of the sealing material. Can be crosslinked in a short time, and foaming (swelling) at each interface of the solar cell module can be further suppressed.
以下、本発明について詳細に説明する。本発明の封止材は、太陽電池モジュールにおいて、光入射側表面に配されるガラス板と基板側に配されるバックシートとを接着し、その間に配された太陽電池用セル(素子)を封止するためのものであって、EVAと、所定の有機過酸化物のみとを含有する。適用対象となる太陽電池モジュールは、上記基本的構成となるものであれば特に限定されず、例えば結晶シリコン太陽電池、多結晶シリコン太陽電池、アモルファスシリコン太陽電池、銅インジウムセレナイド太陽電池、及び化合物半導体太陽電池等が挙げられる。 Hereinafter, the present invention will be described in detail. In the solar cell module, the sealing material of the present invention adheres a glass plate disposed on the light incident side surface and a back sheet disposed on the substrate side, and has a solar cell (element) disposed therebetween. It is for sealing and contains EVA and only a predetermined organic peroxide. The solar cell module to be applied is not particularly limited as long as it has the above basic configuration. For example, a crystalline silicon solar cell, a polycrystalline silicon solar cell, an amorphous silicon solar cell, a copper indium selenide solar cell, and a compound A semiconductor solar cell etc. are mentioned.
(エチレン−酢酸ビニル共重合体)
エチレン−酢酸ビニル共重合体(EVA)は、封止材の主体を成す成分である。EVA中における酢酸ビニルの含有率、すなわち酢酸ビニルより形成される構造単位は、25〜35重量%が好ましい。酢酸ビニルの含有率が35重量%を超えると、粘着性が増大して取り扱いが困難になる。一方、酢酸ビニルの含有率が25重量%未満になると、封止材が硬くなるため加工性が低下し、また、封止材は硬化に伴い緩衝材としての機能が低下するため、封止材で保護されている太陽電池用セルが衝撃により割れやすくなるので好ましくない。
(Ethylene-vinyl acetate copolymer)
Ethylene-vinyl acetate copolymer (EVA) is a component that constitutes the main component of the sealing material. The content of vinyl acetate in EVA, that is, the structural unit formed from vinyl acetate is preferably 25 to 35% by weight. When the vinyl acetate content exceeds 35% by weight, the tackiness increases and handling becomes difficult. On the other hand, when the content of vinyl acetate is less than 25% by weight, the sealing material becomes hard, so that the workability is lowered. Also, the sealing material has a function as a cushioning material as it is cured. Since the solar cell protected by is easily broken by impact, it is not preferable.
(有機過酸化物)
本発明の封止材には、有機過酸化物として、下記一般式(2)で示されるt−ブチル−(2−エチルヘキシル)モノパーオキシカーボネートと下記一般式(1)で示される1,1−ジ(t−アミルパーオキシ)シクロヘキサンが、(1)/(2)の重量比が100/10〜100/70の割合で配合される。有機過酸化物(1)と有機過酸化物(2)を100/10〜100/70の割合で配合することで、封止材の良好な耐候性、接着性、耐熱性などを担保しながら、EVAを短時間で架橋できると共に、さらに太陽電池モジュールの各界面における発泡(膨れ)を抑制できる。
(Organic peroxide)
In the sealing material of the present invention, as an organic peroxide, t-butyl- (2-ethylhexyl) monoperoxycarbonate represented by the following general formula ( 2 ) and 1,1 represented by the following general formula ( 1 ) are used. -Di (t-amylperoxy) cyclohexane is blended at a weight ratio of (1) / (2) of 100/10 to 100/70. By blending the organic peroxide (1) and the organic peroxide (2) at a ratio of 100/10 to 100/70, while ensuring the good weather resistance, adhesiveness, heat resistance, etc. of the sealing material EVA can be crosslinked in a short time, and foaming (blowing) at each interface of the solar cell module can be further suppressed.
封止材中における有機過酸化物の含有量は、EVA100重量部に対して0.1〜3.0重量部とし、より好ましくは0.3〜2.5重量部とする。EVA100重量部に対して有機過酸化物の含有量が0.1重量部未満では、架橋反応後のEVAのゲル分率(架橋度)が低くかったり、架橋時間が長くなるため、実用に適さない。一方、EVA100重量部に対して有機過酸化物の含有量が5.0重量部を超えると、EVAの架橋が速く、太陽電池モジュール製造時の使い勝手が著しく悪くなり、さらには混合有機過酸化物の残存を引き起こす。この混合有機過酸化物の残存は封止材の着色等を引き起こし、封止材の光透過性を低下させるため、封止材の間に配置される太陽電池用セルの受光量が低減し、結果的に太陽電池モジュールにおける光電変換効率が低下する。 Content of the organic peroxide in a sealing material shall be 0.1-3.0 weight part with respect to 100 weight part of EVA, More preferably, you may be 0.3-2.5 weight part. If the content of the organic peroxide is less than 0.1 parts by weight with respect to 100 parts by weight of EVA, the gel fraction (crosslinking degree) of EVA after the crosslinking reaction is low or the crosslinking time is long. Absent. On the other hand, when the content of the organic peroxide exceeds 5.0 parts by weight with respect to 100 parts by weight of EVA, the crosslinking of EVA is fast, and the usability at the time of manufacturing the solar cell module is remarkably deteriorated. Cause the survival of. The remaining of the mixed organic peroxide causes coloring of the sealing material and the like, and decreases the light transmittance of the sealing material, so that the amount of received light of the solar battery cell disposed between the sealing materials is reduced, As a result, the photoelectric conversion efficiency in the solar cell module is lowered.
(その他の添加剤)
本発明の封止材には、必要に応じてその他種々の添加剤を配合することができる。例えば、接着性を高めるためにカップリング剤を配合することができる。カップリング剤としては、例えば有機珪素化合物や有機チタン化合物を挙げることができる。有機珪素化合物としては、ビニル基、メタクリロキシアルキル基、アクリロキシアルキル基、エポキシ基のような反応性有機基と、ハロゲン、アルコキシ基、アセトキシ基のような加水分解性基とを有する化合物を例示できる。具体的には、ビニルトリエトキシシラン、ビニルトリス(β−メトキシエトキシ)シラン、γ−メタクリロキシプロピルメトキシシラン、ビニルトリアセトキシシランのような不飽和基を有する化合物の1種または2種以上を使用できる。カップリング剤は、EVA100重量部に対して、0.1〜10重量部程度、好ましくは0.5〜5重量部程度配合すればよい。
(Other additives)
Various other additives can be blended in the sealing material of the present invention as necessary. For example, a coupling agent can be blended in order to improve adhesiveness. Examples of the coupling agent include organic silicon compounds and organic titanium compounds. Examples of organosilicon compounds include compounds having reactive organic groups such as vinyl groups, methacryloxyalkyl groups, acryloxyalkyl groups, and epoxy groups, and hydrolyzable groups such as halogens, alkoxy groups, and acetoxy groups. it can. Specifically, one or more of compounds having an unsaturated group such as vinyltriethoxysilane, vinyltris (β-methoxyethoxy) silane, γ-methacryloxypropylmethoxysilane, and vinyltriacetoxysilane can be used. . The coupling agent may be blended in an amount of about 0.1 to 10 parts by weight, preferably about 0.5 to 5 parts by weight with respect to 100 parts by weight of EVA.
また、架橋速度や架橋効率を高めるために、架橋助剤を配合することができる。架橋助剤としては、例えばポリアリル化合物やポリ(メタ)アクリロキシ化合物のような多不飽和化合物等を挙げることができる。具体的には、トリアリルイソシアヌレート、トリアリルシアレート、ジアリルフタレート、ジアリルフマレート、ジアリルマレエートのようなポリアリル化合物、エチレングリコールジアクリレート、エチレングリコールジメタクリレートのようなポリ(メタ)アクリロキシ化合物の1種または2種以上を使用できる。 Moreover, in order to improve a crosslinking speed and crosslinking efficiency, a crosslinking adjuvant can be mix | blended. Examples of the crosslinking aid include polyunsaturated compounds such as polyallyl compounds and poly (meth) acryloxy compounds. Specifically, polyallyl compounds such as triallyl isocyanurate, triallyl cyanate, diallyl phthalate, diallyl fumarate, diallyl maleate, poly (meth) acryloxy compounds such as ethylene glycol diacrylate, ethylene glycol dimethacrylate 1 type (s) or 2 or more types can be used.
さらに、本発明の効果を阻害しない範囲で、酸化防止剤、光安定剤、紫外線吸収剤、着色剤などを配合することもできる。酸化防止剤としては、例えばフェノール系安定剤、硫黄系安定剤、燐酸系安定剤などが挙げられる。光安定剤としては、例えばヒンダードアミン系光安定剤等が挙げられる。紫外線吸収剤としては、例えばベンゾフェノン系、ベンゾトリアゾール系等が挙げられる。着色剤としては、例えば酸化チタン等が挙げられる。添加剤として高分子化合物を添加する場合は、比較的分子量の大きい低揮発性のものが好ましい。 Furthermore, antioxidants, light stabilizers, ultraviolet absorbers, colorants, and the like can be blended within a range that does not impair the effects of the present invention. Examples of the antioxidant include a phenol stabilizer, a sulfur stabilizer, and a phosphoric acid stabilizer. Examples of the light stabilizer include hindered amine light stabilizers. Examples of the ultraviolet absorber include benzophenone and benzotriazole. Examples of the colorant include titanium oxide. When a polymer compound is added as an additive, a low volatility compound having a relatively large molecular weight is preferable.
(製造方法)
封止材は、EVA、所定の有機過酸化物、及び必要に応じて適宜配合されるその他の添加剤を含む組成物を、単軸押出機、2軸押出機、バンバリーミキサー、ニーダー、オープンロールなどの汎用の混練装置を使用して、実質的に有機過酸化物が分解しない温度、具体的には50〜110℃程度で混練し、一般的には押出成形やカレンダー成形等によりシート状にされる。シート状とする場合は、その厚みは0.1〜1.0mm程度とすればよい。なお、封止材の形状は、太陽電池モジュールの形状などに合わせて適宜変更可能であり、シート状に限定されるものではない。
(Production method)
The sealing material is a single screw extruder, a twin screw extruder, a Banbury mixer, a kneader, an open roll containing a composition containing EVA, a predetermined organic peroxide, and other additives appropriately blended as necessary. Is kneaded at a temperature at which the organic peroxide is not substantially decomposed, specifically about 50 to 110 ° C., and is generally formed into a sheet by extrusion molding, calendar molding, or the like. Is done. In the case of a sheet shape, the thickness may be about 0.1 to 1.0 mm. In addition, the shape of a sealing material can be suitably changed according to the shape of a solar cell module, etc., and is not limited to a sheet form.
その後は、従来から公知の方法にて太陽電池モジュールを製造すればよい。すなわち、太陽電池用セルを少なくとも2枚の封止材で挟み、その両外側にガラス板及びバックシートを重ね合わせた状態で、有機過酸化物の分解温度以上、具体的には115℃以上、好ましくは120℃以上の温度で加熱・加圧することにより接着・封止することで、太陽電池モジュールを製造できる。なお、より接着性を高めるため、ガラス板やバックシートは予めプライマー処理しておくと好ましい。また、封止材は太陽電池用セルにラミネートしておくこともできる。 Thereafter, the solar cell module may be manufactured by a conventionally known method. That is, sandwiching the solar cell between at least two encapsulants, with the glass plate and the back sheet superimposed on both outer sides, the organic peroxide decomposition temperature or higher, specifically 115 ° C. or higher, Preferably, a solar cell module can be manufactured by bonding and sealing by heating and pressurizing at a temperature of 120 ° C. or higher. In addition, in order to improve adhesiveness, it is preferable that the glass plate or the back sheet is previously primed. Moreover, the sealing material can also be laminated on the solar cell.
加熱は、有機過酸化物がほぼ完全に分解するまで行うことが好ましい。この加熱処理により、EVAが架橋され、封止材とその他の構成要素とが強固に接着される。加熱処理は、二段階で行うこともできる。例えば、真空条件下において1〜5分程度加熱して仮接着を行い、次いで常圧下にてさらに5〜30分程度加熱して完全に接着することもできる。このようにして製造される太陽電池モジュールの封止材においては、EVAの架橋密度の指標となるゲル分率が80%以上、好ましくは90%以上となっていることが好ましい。 Heating is preferably performed until the organic peroxide is almost completely decomposed. By this heat treatment, EVA is crosslinked, and the sealing material and other components are firmly bonded. The heat treatment can also be performed in two stages. For example, it can be temporarily bonded by heating for about 1 to 5 minutes under vacuum conditions, and then further bonded for about 5 to 30 minutes under normal pressure for complete bonding. In the sealing material of the solar cell module manufactured as described above, it is preferable that the gel fraction serving as an index of the crosslinking density of EVA is 80% or more, preferably 90% or more.
EVA(酢酸ビニル含有量28重量%)100重量部に対して、表1,2に示す有機過酸化物を表1,2に示す割合で配合した各種封止材組成物を、80℃で押出成形により加熱圧延することにより0.5mm厚のシート状封止材を形成した。 Various sealing material compositions containing organic peroxides shown in Tables 1 and 2 in proportions shown in Tables 1 and 2 are extruded at 80 ° C. with respect to 100 parts by weight of EVA (vinyl acetate content 28% by weight). A sheet-like sealing material having a thickness of 0.5 mm was formed by heating and rolling by molding.
なお、比較例として使用した有機過酸化物は、下記一般式(3)で表される。
t-アミル-(2-エチルヘキシル)パーオキシモノカーボネート:
t-Amyl- (2-ethylhexyl) peroxymonocarbonate:
得られた各実施例及び比較例の封止材に対して、発泡試験(膨れ性の判定)と、架橋度の指標となるゲル分率の測定を行った。その結果も表1,2に示す。発泡試験及びゲル分率の測定は、以下のようにして行った。 A foaming test (determination of swellability) and measurement of a gel fraction serving as an index of the degree of crosslinking were performed on the obtained sealing materials of Examples and Comparative Examples. The results are also shown in Tables 1 and 2. The foaming test and the measurement of the gel fraction were performed as follows.
<発泡試験>
各実施例および比較例の封止材を、縦3cm×横6cmに切り出し、MSパウチフィルム(株式会社明光商会製)に挟み、加熱してラミネート加工したものを135℃で2分間加熱し、その際に発生するガスによるフィルムの膨れを目視で観察し、評価した。
比較例2と同レベル以下の発泡の場合○、比較例2よりも発泡が顕著な場合を×として評価した。
<Foaming test>
The sealing materials of each Example and Comparative Example were cut into a length of 3 cm × width of 6 cm, sandwiched between MS pouch films (manufactured by Meiko Shokai Co., Ltd.), heated and laminated, and heated at 135 ° C. for 2 minutes. The swelling of the film due to the gas generated at the time was visually observed and evaluated.
The case of foaming below the same level as in Comparative Example 2 was evaluated as x, and the case of foaming more remarkable than Comparative Example 2 was evaluated as x.
<ゲル分率の測定>
各実施例および比較例の封止材を用いて、JSRトレーディング(株)製キュラストメーターV型により、135℃で2分架橋を行った。架橋後のEVA封止材を秤量し(Xg)、これを110℃のキシレン中に12時間浸漬して、110℃のキシレン中で洗浄・乾燥させた200メッシュの金網で不溶解分をろ過し、金網上の残渣を真空乾燥して乾燥残渣の重量を測定し(Yg)、ゲル分率を算出した(ゲル分率(重量%)=(Y/X)×100)。
<Measurement of gel fraction>
Using the encapsulant of each example and comparative example, crosslinking was performed at 135 ° C. for 2 minutes using a curast meter V type manufactured by JSR Trading Co., Ltd. The EVA sealing material after cross-linking is weighed (Xg), immersed in xylene at 110 ° C. for 12 hours, and the insoluble matter is filtered through a 200 mesh wire net washed and dried in xylene at 110 ° C. The residue on the wire net was vacuum dried, the weight of the dried residue was measured (Yg), and the gel fraction was calculated (gel fraction (% by weight) = (Y / X) × 100).
表1の結果から明らかなように、EVAに対して一般式(1)および(2)で示される所定の有機過酸化物を(1)/(2)の重量比が100/10〜100/70で配合した封止材であれば、スコーチや発泡を抑制することができ、ゲル分率が80%以上となる太陽電池用封止材が得られた。一方、比較例1においては、有機過酸化物が5.0重量部含まれているため、熱分解によるガスの発生量が多く発泡が生じた。比較例2および3においては、有機過酸化物(1)の重量比が少ないため架橋時間が2分でのゲル分率が80%に達しなかった。比較例4においては、有機過酸化物の熱分解によりガスが発生し発泡が生じ、架橋時間の短縮も困難であった。 As is clear from the results in Table 1, the predetermined organic peroxide represented by the general formulas (1) and (2) with respect to EVA has a weight ratio of (1) / (2) of 100/10 to 100 / If it was the sealing material mix | blended by 70, scorch and foaming could be suppressed and the sealing material for solar cells from which a gel fraction will be 80% or more was obtained. On the other hand, in Comparative Example 1, since 5.0 parts by weight of the organic peroxide was contained, the amount of gas generated by thermal decomposition was large and foaming occurred. In Comparative Examples 2 and 3, since the weight ratio of the organic peroxide (1) was small, the gel fraction at a crosslinking time of 2 minutes did not reach 80%. In Comparative Example 4, gas was generated due to thermal decomposition of the organic peroxide, foaming occurred, and it was difficult to shorten the crosslinking time.
101 太陽電池用セル
102 ガラス板
103 バックシート
104 封止材
101
Claims (2)
前記有機過酸化物として、下記一般式で示される有機過酸化物(1)と有機過酸化物(2)の重量比が、(1)/(2)=100/10〜100/70であることを特徴とする、太陽電池モジュール用封止材。
As the organic peroxide, the weight ratio of the organic peroxide (1) and the organic peroxide (2) represented by the following general formula is (1) / (2) = 100/10 to 100/70. The sealing material for solar cell modules characterized by the above-mentioned.
The sealing material for solar cell modules according to claim 1, wherein the content of the organic peroxide is 0.3 to 3.0 parts by weight with respect to 100 parts by weight of the EVA.
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