KR101212449B1 - Resin coating composition for solar cell module back sheet, solar cell module back sheet, solar cell comprising the same, and fabrication method thereof - Google Patents
Resin coating composition for solar cell module back sheet, solar cell module back sheet, solar cell comprising the same, and fabrication method thereof Download PDFInfo
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- KR101212449B1 KR101212449B1 KR1020100103122A KR20100103122A KR101212449B1 KR 101212449 B1 KR101212449 B1 KR 101212449B1 KR 1020100103122 A KR1020100103122 A KR 1020100103122A KR 20100103122 A KR20100103122 A KR 20100103122A KR 101212449 B1 KR101212449 B1 KR 101212449B1
- Authority
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- Prior art keywords
- solar cell
- cell module
- back sheet
- plate
- resin
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- 229920005989 resin Polymers 0.000 title claims abstract description 64
- 239000011347 resin Substances 0.000 title claims abstract description 64
- 238000000034 method Methods 0.000 title claims description 20
- 239000008199 coating composition Substances 0.000 title abstract description 19
- 238000004519 manufacturing process Methods 0.000 title abstract description 6
- 239000002245 particle Substances 0.000 claims abstract description 28
- 239000000758 substrate Substances 0.000 claims abstract description 23
- -1 silicate compound Chemical class 0.000 claims abstract description 21
- 239000011247 coating layer Substances 0.000 claims abstract description 15
- 239000010410 layer Substances 0.000 claims description 39
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims description 21
- 229910001701 hydrotalcite Inorganic materials 0.000 claims description 15
- 229960001545 hydrotalcite Drugs 0.000 claims description 15
- GDVKFRBCXAPAQJ-UHFFFAOYSA-A dialuminum;hexamagnesium;carbonate;hexadecahydroxide Chemical compound [OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Al+3].[Al+3].[O-]C([O-])=O GDVKFRBCXAPAQJ-UHFFFAOYSA-A 0.000 claims description 14
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- KKEYFWRCBNTPAC-UHFFFAOYSA-L terephthalate(2-) Chemical compound [O-]C(=O)C1=CC=C(C([O-])=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-L 0.000 claims description 3
- 239000000463 material Substances 0.000 claims description 2
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 27
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- 229910052731 fluorine Inorganic materials 0.000 description 27
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- 238000011084 recovery Methods 0.000 description 20
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- 238000000576 coating method Methods 0.000 description 19
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- 238000001035 drying Methods 0.000 description 8
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- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
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- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 4
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- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- 239000006087 Silane Coupling Agent Substances 0.000 description 3
- 229910000278 bentonite Inorganic materials 0.000 description 3
- 239000000440 bentonite Substances 0.000 description 3
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 3
- 230000005540 biological transmission Effects 0.000 description 3
- 239000004927 clay Substances 0.000 description 3
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 3
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 2
- 229910001596 celadonite Inorganic materials 0.000 description 2
- GUJOJGAPFQRJSV-UHFFFAOYSA-N dialuminum;dioxosilane;oxygen(2-);hydrate Chemical compound O.[O-2].[O-2].[O-2].[Al+3].[Al+3].O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O GUJOJGAPFQRJSV-UHFFFAOYSA-N 0.000 description 2
- 238000000635 electron micrograph Methods 0.000 description 2
- 229910000271 hectorite Inorganic materials 0.000 description 2
- KWLMIXQRALPRBC-UHFFFAOYSA-L hectorite Chemical compound [Li+].[OH-].[OH-].[Na+].[Mg+2].O1[Si]2([O-])O[Si]1([O-])O[Si]([O-])(O1)O[Si]1([O-])O2 KWLMIXQRALPRBC-UHFFFAOYSA-L 0.000 description 2
- 229910052900 illite Inorganic materials 0.000 description 2
- 230000006872 improvement Effects 0.000 description 2
- 238000010030 laminating Methods 0.000 description 2
- 229910052901 montmorillonite Inorganic materials 0.000 description 2
- VGIBGUSAECPPNB-UHFFFAOYSA-L nonaaluminum;magnesium;tripotassium;1,3-dioxido-2,4,5-trioxa-1,3-disilabicyclo[1.1.1]pentane;iron(2+);oxygen(2-);fluoride;hydroxide Chemical compound [OH-].[O-2].[O-2].[O-2].[O-2].[O-2].[F-].[Mg+2].[Al+3].[Al+3].[Al+3].[Al+3].[Al+3].[Al+3].[Al+3].[Al+3].[Al+3].[K+].[K+].[K+].[Fe+2].O1[Si]2([O-])O[Si]1([O-])O2.O1[Si]2([O-])O[Si]1([O-])O2.O1[Si]2([O-])O[Si]1([O-])O2.O1[Si]2([O-])O[Si]1([O-])O2.O1[Si]2([O-])O[Si]1([O-])O2.O1[Si]2([O-])O[Si]1([O-])O2.O1[Si]2([O-])O[Si]1([O-])O2 VGIBGUSAECPPNB-UHFFFAOYSA-L 0.000 description 2
- 229910000273 nontronite Inorganic materials 0.000 description 2
- UZLYXNNZYFBAQO-UHFFFAOYSA-N oxygen(2-);ytterbium(3+) Chemical compound [O-2].[O-2].[O-2].[Yb+3].[Yb+3] UZLYXNNZYFBAQO-UHFFFAOYSA-N 0.000 description 2
- 229910000275 saponite Inorganic materials 0.000 description 2
- 229910000077 silane Inorganic materials 0.000 description 2
- 150000004760 silicates Chemical class 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- 229910003454 ytterbium oxide Inorganic materials 0.000 description 2
- 229940075624 ytterbium oxide Drugs 0.000 description 2
- XASAPYQVQBKMIN-UHFFFAOYSA-K ytterbium(iii) fluoride Chemical compound F[Yb](F)F XASAPYQVQBKMIN-UHFFFAOYSA-K 0.000 description 2
- 239000011787 zinc oxide Substances 0.000 description 2
- FAIFRACTBXWXGY-JTTXIWGLSA-N COc1ccc2C[C@H]3N(C)CC[C@@]45[C@@H](Oc1c24)[C@@]1(OC)C=C[C@@]35C[C@@H]1[C@](C)(O)CCc1ccccc1 Chemical compound COc1ccc2C[C@H]3N(C)CC[C@@]45[C@@H](Oc1c24)[C@@]1(OC)C=C[C@@]35C[C@@H]1[C@](C)(O)CCc1ccccc1 FAIFRACTBXWXGY-JTTXIWGLSA-N 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- 150000007945 N-acyl ureas Chemical class 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229910052788 barium Inorganic materials 0.000 description 1
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 1
- 230000004888 barrier function Effects 0.000 description 1
- 230000000903 blocking effect Effects 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- CRHLEZORXKQUEI-UHFFFAOYSA-N dialuminum;cobalt(2+);oxygen(2-) Chemical compound [O-2].[O-2].[O-2].[O-2].[O-2].[Al+3].[Al+3].[Co+2].[Co+2] CRHLEZORXKQUEI-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 239000011229 interlayer Substances 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 239000012948 isocyanate Substances 0.000 description 1
- 150000002513 isocyanates Chemical class 0.000 description 1
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- 229920001225 polyester resin Polymers 0.000 description 1
- 239000004645 polyester resin Substances 0.000 description 1
- 229920001021 polysulfide Polymers 0.000 description 1
- 239000005077 polysulfide Substances 0.000 description 1
- 150000008117 polysulfides Polymers 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 125000005504 styryl group Chemical group 0.000 description 1
- PXQLVRUNWNTZOS-UHFFFAOYSA-N sulfanyl Chemical class [SH] PXQLVRUNWNTZOS-UHFFFAOYSA-N 0.000 description 1
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- 238000004381 surface treatment Methods 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
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- 239000005341 toughened glass Substances 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 230000037303 wrinkles Effects 0.000 description 1
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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
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D7/00—Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
- C09D7/40—Additives
- C09D7/60—Additives non-macromolecular
- C09D7/61—Additives non-macromolecular inorganic
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B27/00—Layered products comprising a layer of synthetic resin
- B32B27/36—Layered products comprising a layer of synthetic resin comprising polyesters
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D7/00—Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
- C09D7/40—Additives
- C09D7/66—Additives characterised by particle size
- C09D7/68—Particle size between 100-1000 nm
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D7/00—Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
- C09D7/40—Additives
- C09D7/66—Additives characterised by particle size
- C09D7/69—Particle size larger than 1000 nm
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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
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D7/00—Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
- C09D7/40—Additives
- C09D7/70—Additives characterised by shape, e.g. fibres, flakes or microspheres
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L31/00—Semiconductor 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
- H01L31/04—Semiconductor 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
- H01L31/042—PV modules or arrays of single PV cells
- H01L31/048—Encapsulation of modules
- H01L31/049—Protective back sheets
-
- H—ELECTRICITY
- H02—GENERATION; CONVERSION OR DISTRIBUTION OF ELECTRIC POWER
- H02S—GENERATION OF ELECTRIC POWER BY CONVERSION OF INFRARED RADIATION, VISIBLE LIGHT OR ULTRAVIOLET LIGHT, e.g. USING PHOTOVOLTAIC [PV] MODULES
- H02S20/00—Supporting structures for PV modules
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2457/00—Electrical equipment
- B32B2457/12—Photovoltaic modules
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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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- Chemical & Material Sciences (AREA)
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- Nanotechnology (AREA)
- Condensed Matter Physics & Semiconductors (AREA)
- Physics & Mathematics (AREA)
- Electromagnetism (AREA)
- General Physics & Mathematics (AREA)
- Computer Hardware Design (AREA)
- Microelectronics & Electronic Packaging (AREA)
- Power Engineering (AREA)
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- Laminated Bodies (AREA)
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Abstract
본 발명은 수지와 판상입자를 함유하는 태양전지모듈 백시트용 수지코팅조성물, 기재 및 상기 기재의 양면 또는 일면에 코팅된 판상입자 또는 층상형 규산염 화합물을 함유하는 수지코팅층을 포함하는 태양전지모듈용 백시트, 상기 백시트를 포함하는 태양전지모듈 및 이의 제조방법을 제공한다.The present invention relates to a solar cell module comprising a resin coating composition for a solar cell module back sheet containing a resin and a plate particle, a substrate and a resin coating layer containing a plate particle or a layered silicate compound coated on both or one side of the substrate. It provides a back sheet, a solar cell module including the back sheet and a method of manufacturing the same.
Description
본 발명은 태양전지모듈 백시트용 수지코팅조성물에 관한 것으로, 보다 상세하게는 절연성과 흡습성이 우수한 태양전지모듈용 백시트 수지코팅조성물, 태양전지모듈용 백시트, 이를 포함하는 태양전지모듈 및 이의 제조방법에 관한 것이다.
The present invention relates to a resin coating composition for a solar cell module back sheet, and more particularly, a back sheet resin coating composition for a solar cell module having excellent insulation and hygroscopicity, a solar cell module back sheet, a solar cell module including the same, and a It relates to a manufacturing method.
태양전지모듈은 저철분 강화유리, 충진재(EVA), 태양전지(Cell), 백시트(Back sheet)와 각 셀을 전기적으로 연결시켜 주는 금속 재질의 와이어로 구성되어 있으며, 백시트의 기능으로는 최 후면에서 침투하는 습기를 막는 방습기능 및 절연 차단기능으로 하는 태양전지모듈의 구성 재료이다.The solar cell module consists of low iron tempered glass, filler (EVA), solar cell (Cell), back sheet, and metal wire that electrically connects each cell. It is a constituent material of the solar cell module which has moisture proof function and insulation blocking function to prevent moisture penetrating from the rear.
백시트의 주요 성능 및 구조로는 25년 이상 장기 내구성(내후성)을 가져야 하며, 수증기 침투 방지 효과(흡습성)가 1.6g/m2(24hr) 이하, 접착층 및 기재와의 접착 강도가 높아야 한다.As the main performance and structure of the backsheet, it must have long term durability (weather resistance) for 25 years or more, the water vapor penetration prevention effect (hygroscopicity) should be 1.6g / m 2 (24hr) or less, and the adhesive strength with the adhesive layer and the substrate should be high.
따라서 현재는 내후성이 우수한 PVF(Polyvinyl Fluoride : TEDLAR) 시트를 라미네이팅하는 타입의 제품이 사용되고 있으나 비용이 높아 비용절감을 위해 PET 필름에 알루미늄 라미네이팅(혹은 증착)하는 타입과 불소수지 코팅 등의 PET 복합 구조 타입의 제품이 일본기업을 중심으로 개발 및 상품화되는 추세이나, 가장 중요한 흡습성이 떨어져 두께가 두꺼워지고, 이로 인해 백시트 및 태양전지 자체의 두께를 얇게 가져 갈수 없는 문제점이 있으며, 절연성 또한 좋지 않다.
Therefore, the type of laminating the PVF (Polyvinyl Fluoride: TEDLAR) sheet with excellent weather resistance is currently used, but the PET composite structure such as aluminum laminating (or deposition) on PET film for cost reduction due to high cost The type of products are being developed and commercialized mainly by Japanese companies, but the most important hygroscopicity is reduced, resulting in a thicker thickness, which makes it difficult to take the thickness of the backsheet and the solar cell itself, and the insulation is also poor.
본 발명은 상기한 바와 같은 종래기술이 가지는 문제를 해결하기 위해 안출된 것으로, 그 목적은 절연성과 흡습성이 우수한 태양전지모듈 백시트용 수지코팅조성물, 태양전지용 백시트, 이를 포함하는 태양전지 및 이의 제조방법을 제공함에 있다.
The present invention has been made to solve the problems of the prior art as described above, the object is a resin coating composition for a solar cell module back sheet excellent in insulation and hygroscopicity, a solar cell back sheet, a solar cell comprising the same To provide a manufacturing method.
상기한 바와 같은 본 발명의 기술적 과제는 다음과 같은 수단에 의해 달성되어진다.The technical problem of the present invention as described above is achieved by the following means.
(1) 수지와 판상입자 또는 층상형 규산염 화합물을 함유하는 태양전지모듈 백시트용 수지코팅조성물.
(1) Resin coating composition for solar cell module backsheet containing resin, plate particle, or layered silicate compound.
(2) 제 1항에 있어서, (2) The method according to claim 1,
판상입자는 판상 알루미나 또는 판상 하이드로 탈사이트인 것을 특징으로 하는 태양전지모듈 백시트용 수지코팅조성물.
Plate-like particles are resin coating composition for solar cell module back sheet, characterized in that the plate-shaped alumina or plate-like hydrotalcite.
(3) 제 1항에 있어서, (3) The method according to claim 1,
층상형 규산염 화합물은 몬모릴로나이트(montmorillonite), 논트로나이트(nontronite), 바이델라이트(beidellite), 헥토나이트(hectorite), 사포나이트(saponite), 일나이트(illite), 셀라토나이트(celadonite), 글로코나이트(gluconite), 점토(clay) 및 벤토나이트(bentonite)인 것을 특징으로 하는 태양전지모듈 백시트용 수지코팅조성물.
Layered silicate compounds include montmorillonite, nontronite, beidelite, hectorite, saponite, illite, celadonite, writing Resin coating composition for a solar cell module backsheet, characterized in that the loconite (gluconite), clay (clay) and bentonite (bentonite).
(4) 제 1항에 있어서, (4) The method according to 1,
실리카, 산화 티탄, 산화 아연, 황산 바륨, 산화 이터븀, 및 불화 이터븀의 군에서 선택된 적어도 1종을 더 포함하는 것을 특징으로 하는 태양전지모듈 백시트용 수지코팅조성물.
A resin coating composition for a solar cell module back sheet, further comprising at least one selected from the group consisting of silica, titanium oxide, zinc oxide, barium sulfate, ytterbium oxide, and ytterbium fluoride.
(5) 기재; 및 (5) substrates; And
상기 기재의 양면 또는 일면에 코팅된 판상입자 또는 층상형 규산염 화합물을 함유하는 수지코팅층Resin coating layer containing plate-like particles or layered silicate compound coated on both or one side of the substrate
을 포함하는 태양전지모듈용 백시트.
Back sheet for a solar cell module comprising a.
(6) 제 5항에 있어서,(6) the method of paragraph 5,
기재는 폴리에스테르테레프탈레이트(PET) 필름인 것을 특징으로 하는 태양전지모듈용 백시트.
The substrate is a polyester terephthalate (PET) film, characterized in that the solar cell module back sheet.
(7) 제 5항에 있어서, (7) The method of paragraph 5,
판상입자는 판상 알루미나 또는 판상 하이드로 탈사이트인 것을 특징으로 하는 태양전지모듈용 백시트.
The plate particle is a solar cell module back sheet, characterized in that the plate-shaped alumina or plate-like hydrotalcite.
(8) 제 5항에 있어서, (8) the method of paragraph 5,
판상입자는 장축대 단축의 비(Aspect ratio)가 5~300인 것을 특징으로 하는 태양전지모듈용 백시트.
The plate-shaped particle is a back sheet for a solar cell module, characterized in that the aspect ratio of the axis short axis (5 ~ 300).
(9) 제 5항에 있어서,(9) The method of claim 5,
판상입자는 장축이 0.2~30㎛, 단축이 0.01~5㎛인 것을 특징으로 하는 태양전지모듈용 백시트.
The plate-shaped particle is a back sheet for a solar cell module, characterized in that the major axis is 0.2 ~ 30㎛, the minor axis is 0.01 ~ 5㎛.
(10) 제 5항에 있어서,(10) The method according to 5,
수지코팅층의 표면거칠기는 0.3~5.0㎛인 것을 특징으로 하는 태양전지모듈용 백시트.
The surface roughness of the resin coating layer is a back sheet for a solar cell module, characterized in that 0.3 ~ 5.0㎛.
(11) 제 5항에 있어서,(11) The method according to 5,
수지코팅층의 상면에 프라이머층이 더 형성된 것을 특징으로 하는 태양전지모듈용 백시트.
The solar cell module back sheet, characterized in that the primer layer is further formed on the upper surface of the resin coating layer.
(12) 제 5항에 있어서,(12) The method according to 5,
판상입자 또는 층상형 규산염 화합물은 수지 중량에 대하여 1~50 중량% 포함된 것을 특징으로 하는 태양전지모듈용 백시트.
Plate-like particles or layered silicate compound is a solar cell module back sheet, characterized in that contained 1 to 50% by weight based on the weight of the resin.
(13) 제 5항 내지 제 12항에서 선택된 어느 한 항의 백시트를 포함하는 태양전지모듈.
(13) A solar cell module comprising the backsheet of any one of claims 5-12.
(14) 기재를 준비하는 단계; 및 (14) preparing a substrate; And
상기 기재의 양면 또는 일면에 판상입자 또는 층상형 규산염 화합물을 함유하는 수지를 코팅하는 단계를 포함하는 태양전지모듈용 백시트의 제조방법.
A method of manufacturing a back sheet for a solar cell module comprising coating a resin containing a plate-like particle or a layered silicate compound on both surfaces or one surface of the substrate.
(15) 제 14항에 있어서, (15) The method according to
판상입자는 판상 알루미나 또는 판상 하이드로 탈사이트인 것을 특징으로 하는 태양전지모듈용 백시트의 제조방법.The plate-like particle is a manufacturing method of a solar cell module back sheet, characterized in that the plate-shaped alumina or plate-like hydrotalcite.
상기 본 발명에 의하면 절연성과 흡습성이 모두 우수한 태양전지모듈용 백시트 및 이를 포함하는 태양전지모듈을 제공할 수 있다
According to the present invention can provide a solar cell module back sheet excellent in both insulation and hygroscopicity and a solar cell module comprising the same.
도 1은 본 발명에 따른 태양전지모듈용 백시트의 구성도이다.
도 1은 본 발명에 사용된 판상 알루미나의 전자현미경사진이다.
도 2는 본 발명에 사용된 구형이 산화티탄의 전자현미경사진이다.1 is a block diagram of a solar cell module back sheet according to the present invention.
1 is an electron micrograph of the plate-shaped alumina used in the present invention.
2 is an electron micrograph of the spherical titanium oxide used in the present invention.
이하 본 발명의 내용을 보다 상세하게 설명하면 다음과 같다.Hereinafter, the content of the present invention will be described in detail.
본 발명은 수지와 판상입자 또는 층상형 규산염 화합물을 함유하는 태양전지모듈 백시트용 수지코팅조성물을 제공한다.The present invention provides a resin coating composition for a solar cell module backsheet containing a resin and a plate-like particle or layered silicate compound.
상기 수지코팅조성물에 사용되는 수지는 특별한 종류로 한정을 요하는 것은 아니며 예를 들어, 불소계수지, 폴리에스테르계 수지 등이 사용되어질 수 있다. The resin used in the resin coating composition is not limited to a special kind, and for example, a fluorine resin, a polyester resin, or the like may be used.
상기 수지코팅조성물에 사용되는 판상입자로는 바람직하게는 판상 무기입자, 예를 들어 판상 알루미나 또는 판상 하이드로탈사이트 등이 사용될 수 있다.As the plate-shaped particles used in the resin coating composition, plate-like inorganic particles, for example, plate-like alumina or plate-like hydrotalcite may be used.
상기 수지코팅조성물에 사용되는 층상형 규산염 화합물로는 바람직하게는 층간 화합물인 무기입자, 예를 들어 몬모릴로나이트(montmorillonite), 논트로나이트(nontronite), 바이델라이트(beidellite), 헥토나이트(hectorite), 사포나이트(saponite), 일나이트(illite), 셀라토나이트(celadonite), 글로코나이트(gluconite), 점토(clay) 및 벤토나이트(bentonite) 등이 사용될 수 있다.The layered silicate compound used in the resin coating composition is preferably an inorganic particle that is an interlayer compound, for example, montmorillonite, nontronite, beidelite, hectorite, Saponite, illite, celadonite, gluconite, clay and bentonite may be used.
흡습성을 개선하기 위하여 상기 판상입자, 바람직하게는 판상 알루미나 또는 판상 하이드로 탈사이트, 또는 층상형 규산염 화합물의 함유량은 수지 함량에 대하여 1 중량% 이상 함유하는 것이 바람직하고, 보다 바람직하게는 10 중량% 이상이며, 더욱 바람직하게는 10~50 중량%를 함유하는 좋다. 수지 함량에 대하여 1 중량% 이하일 경우 흡습성 및 절연성을 확보하기 어려우며, 50 중량% 이상일 경우 코팅성이 떨어지며, 기재의 접착성을 확보하기가 어려운 단점이 있다.In order to improve hygroscopicity, the content of the plate-like particles, preferably plate-like alumina or plate-hydrotalcite, or layered silicate compound is preferably contained in an amount of 1% by weight or more based on the resin content, more preferably 10% by weight or more. It is good to contain 10-50 weight% more preferably. If it is 1 wt% or less with respect to the resin content, it is difficult to secure hygroscopicity and insulation, and if it is 50 wt% or more, the coating property is poor, and it is difficult to secure adhesion of the substrate.
상기 판상입자의 사이즈는 바람직하게는 장축이 0.2~30 ㎛, 단축이 0.01~5 ㎛인 것으로 하며, 장축대 단축의 비(Aspect ratio)가 5~300, 바람직하게는 10 이상이며, 보다 바람직하게는 30 이상인 것에서 선택하는 것이 좋다. 장축대 단축의 비가 5보다 작을 경우 판상 입자의 층간 구조를 이루지 못해 흡습성 향상에 한계가 있으며, 장축대 단축의 비가 300 이상일 경우 입자 사이즈가 수십 마이크론으로 코팅 두께를 얇게 가져 갈 수 없는 단점이 있다.Preferably the size of the plate-shaped particles is 0.2 ~ 30 ㎛ long axis, 0.01 ~ 5 ㎛ short axis, the aspect ratio of long axis short axis is 5 ~ 300, preferably 10 or more, more preferably It is good to select from 30 or more. If the ratio of the short axis length is less than 5, there is a limit in improving hygroscopicity because the interlaminar structure of the plate-shaped particles is not achieved. If the ratio of the long axis length ratio is 300 or more, the particle size is tens of microns.
한편 상기 수지코팅층의 상부는 접착층(예를 들어 EVA 필름)과의 접착력을 부여하기 위해 코팅층의 표면거칠기를 0.3~5.0 ㎛로 형성하는 것이 좋으며, 표면거칠기를 부여하지 않은 경우 프라이머(Primer)를 처리하여 접착력을 부여할 수도 있다. 표면거칠기가 0.3 ㎛ 이하일 경우 상부 필름과의 접착력이 떨어질 수 있으며, 5 ㎛ 이상일 경우 상부 필름과의 접착력이 떨어질 뿐만 아니라, 공기층이 생겨 흡습성이 떨어질 가능성이 있다.On the other hand, the upper surface of the resin coating layer is preferably formed to form a surface roughness of 0.3 ~ 5.0 ㎛ of the coating layer in order to give an adhesive force with the adhesive layer (for example EVA film), if the surface roughness is not given a primer (Primer) treatment It can also give an adhesive force. When the surface roughness is 0.3 μm or less, the adhesive force with the upper film may be degraded, and when the surface roughness is 5 μm or more, the adhesive force with the upper film may be degraded, and an air layer may be formed to reduce the hygroscopicity.
상기 수지코팅층의 조성에는 판상입자 또는 층상형 규산염 화합물 이외에 UV 차단성(내후성 개선 포함), 표면 거칠기 조정, 도막상의 기포 또는 주름 발생의 억제, 백색도 향상 등을 위해 실리카, 산화 티탄, 산화 아연, 황산 바륨, 산화 이터븀, 불화 이터븀 등의 미립자를 혼합하여 사용할 수 있으며, 색상 구현을 위해 산화철(Red), 코발트 알루미네이트(Blue), 코발트 망간 알루미네이트(Greem) 등의 미립자를 혼합하여 사용할 수도 있다.The resin coating layer may include silica, titanium oxide, zinc oxide, and sulfuric acid for the purpose of UV barrier property (including weather resistance improvement), surface roughness adjustment, suppression of bubbles or wrinkles on the coating film, whiteness improvement, etc. in addition to the plate-shaped particles or the layered silicate compound. Particles such as barium, ytterbium oxide, and ytterbium fluoride can be mixed and used, and fine particles such as iron oxide (Red), cobalt aluminate (Blue), and cobalt manganese aluminate (Greem) can also be used for color realization. have.
또한 상기 판상입자 또는 층상형 규산염 화합물의 경우 불소수지와의 혼화성을 향상시키기 위해 실란커플링제(Silane coupling agent) 등을 사용할 수 있으며, 사용되는 실란의 관능기는 비닐계, 에폭시계, 스티릴계, 메타크릴옥시계, 아크릴옥시계, 아미노계, 유레이드계(Ureid), 클로로프로필계, 메르캅토계, 폴리설파이드계, 이소시아네이트계 등을 사용할 수 있다. 이때 실란커플링제의 표면 처리량은 하기 식에 따라 결정되어질 수 있다. In addition, in the case of the plate-like particles or the layered silicate compound, a silane coupling agent may be used to improve the miscibility with the fluororesin, and the functional groups of the silane used may be vinyl, epoxy, styryl, Methacrylicoxy type, acryloxy type, amino type, ureide type (Ureid), chloropropyl type, mercapto type, polysulfide type, isocyanate type etc. can be used. At this time, the surface treatment amount of the silane coupling agent may be determined according to the following formula.
실란함유량(g) = (필러의 양(g)×필러표면적(㎡/g)/(실란커플링제의 최소코팅면적(ws))
Silane Content (g) = (Amount of Filler (g) x Filler Surface Area (m2 / g) / (Minimum Coating Area of Silane Coupling Agent (ws))
또한, 본 발명은 도 1에 도시된 바와 같은 태양전지용 백시트를 포함하며, 이때 백시트는 기재(10); 및 상기 기재의 양면 또는 한면에 코팅된 판상입자 또는 층상형 규산염 화합물을 함유하는 수지코팅층(20)을 포함한다.In addition, the present invention includes a solar cell backsheet as shown in Figure 1, wherein the backsheet is a substrate (10); And a
상기 본 발명에 따른 태양전지용 백시트를 구성하는 기재로는 특별히 한정되는 것은 아니며, 폴리에스테르계 필름, 바람직하게는 폴리에스테르테레프탈레이트(PET) 필름이 사용되어질 수 있다.The substrate constituting the solar cell backsheet according to the present invention is not particularly limited, and a polyester-based film, preferably a polyester terephthalate (PET) film, may be used.
상기 판상입자 또는 층상형 규산염 화합물이 함유된 수지코팅층은 수지와 판상입자 또는 층상형 규산염 화합물이 일정비율로 조성된 조성물을 기재 필름의 양면 또는 일면에 코팅하여 형성할 수 있으며, 이때 코팅은 닥터 블레이드 또는 슬롯다이, 콤마 등의 코팅 장비를 사용하여 코팅 두께를 5~50 ㎛로 조절하는 것이 바람직하며, 더욱 바람직하게는 20~30㎛로 조절한다.The resin coating layer containing the plate-like particles or the layered silicate compound may be formed by coating a composition including a resin and the plate-like particles or the layered silicate compound in a constant ratio on both sides or one side of the base film, wherein the coating is a doctor blade. Or it is preferable to adjust the coating thickness to 5 ~ 50㎛, more preferably 20 ~ 30㎛ using a coating equipment such as slot die, comma.
상기와 같이 수지코팅 조성물을 기재에 코팅한 후 60 ~ 300℃의 온도 바람직하게는 250℃에서 10분 이상 건조시키는 단계를 추가로 포함할 수 있다.After coating the resin coating composition on the substrate as described above may further comprise a step of drying at a temperature of 60 ~ 300 ℃ preferably 250
본 발명에 따른 태양전지용 백시트는 접착층/프라이머층/수지코팅층/기재코팅층/수지코팅층/프라이머층/접착층을 기본 구조로 하며, 이때 진공 접착할 경우에는 접착층은 생략할 수도 있다. 앞에서 언급한 바와 같이 수지코팅층 및 접착층은 기재 필름의 상부에만 형성하고 하부에는 생략할 수도 있다.The solar cell backsheet according to the present invention has an adhesive layer / primer layer / resin coating layer / base coating layer / resin coating layer / primer layer / adhesive layer as a basic structure, and in this case, the adhesive layer may be omitted when vacuum bonding. As mentioned above, the resin coating layer and the adhesive layer may be formed only on the upper portion of the base film, and may be omitted below.
상기와 같이 제조되는 본 발명에 따른 백시트는 흡습율(Water vapor Transmission(WVTR))이 1 g/m2d 이하인 것이 바람직하며, 더욱 좋게는 0.3 g/m2d 이하인 것이 바람직하며, 더더욱 좋게는 0.1 g/m2d 이하인 것이 바람직하다. 일반적으로 필름의 흡습율은 PET의 경우 2.3 g/m2d 이며, PVF(Tadlar)/PET/PVF(Tadlar)의 경우 3.0 g/m2d 이며, EVA의 경우 27~33 g/m2d 의 흡습성을 갖는다.
It is preferable that the backsheet according to the present invention prepared as described above has a water vapor transmission (WVTR) of 1 g / m 2 d or less, more preferably 0.3 g / m 2 d or less, and even better. Is preferably 0.1 g / m 2 d or less. In general, the moisture absorption rate of the film was 2.3 g / m 2 d when the PET, PVF (Tadlar) / PET / PVF For (Tadlar) and 3.0 g / m 2 d, 27 ~ 33 g / m 2 d when the EVA It has hygroscopicity.
또한, 본 발명은 상기 태양전지 백시트를 포함하는 태양전지를 제공한다.In addition, the present invention provides a solar cell comprising the solar cell back sheet.
본 발명에 따른 태양전지는 직렬 또는 병렬로 배치된 태양전지 셀 주변을 열가소성 플라스틱(에틸렌-비닐아세테이트 공중합체)으로 구성된 충전재로 간격을 메우고, 태양광이 부딪히는 면에는 유리면이 배치되며, 이면은 본 발명에 따른 태양전지 백시트로 보호하는 구성을 가질 수 있다.The solar cell according to the present invention fills a gap with a filler composed of a thermoplastic (ethylene-vinylacetate copolymer) around the solar cells arranged in series or in parallel, and a glass surface is disposed on the side where the solar light collides. It may have a configuration to protect the solar cell back sheet according to the invention.
상기 태양전지는 본 발명에 따른 태양전지 백시트를 포함하는 것을 제외하고, 당 기술분야에 알려진 방법으로 제조할 수 있으며, 이에 따라 제조된 태양전지는 절연성 및 흡습성이 매우 우수하다.
The solar cell may be manufactured by a method known in the art, except for including the solar cell backsheet according to the present invention, and thus the solar cell is very excellent in insulation and hygroscopicity.
이하 본 발명의 내용을 실시예를 통해 구체적으로 설명하고자 하나 본 발명의 권리범위는 이들 실시예에 의해 한정되는 것은 아니다.
Hereinafter, the contents of the present invention will be described in detail with reference to examples, but the scope of the present invention is not limited to these examples.
[실시예 1] Example 1
불소계 수지로 Lumifron LF-200(Asahi Glass, Solvent soluble Fluoropolymer, 고형분 60중량%) 404g, 판상 알루미나(도 1, SG-FALO2000, SukgyungAT) 526g, 크실렌 334g을 플레니터리 믹서(NETESCH)를 사용하여 혼합하였다.404 g of Lumifron LF-200 (Asahi Glass, Solvent soluble Fluoropolymer, 60 wt% solids), plate-shaped alumina (FIG. 1, SG-FALO2000, SukgyungAT), and xylene 334 g were mixed with a fluorine resin using a planetary mixer (NETESCH). It was.
상기 혼합된 슬러리를 3-롤 밀(EXAKT)을 사용하여 밀링하여 균일하게 혼합한 후 20㎛ 마이크로 필터로 여과한 후 회수율을 계산하였다. (회수율 = [1차분산 필터링 후 회수량 /1차분산 투입량]×100) (ex) 회수율 % = [A/1264]×100)The mixed slurry was milled using a three-roll mill (EXAKT), uniformly mixed, filtered with a 20 μm micro filter, and then the recovery was calculated. (Recovery rate = [recovery amount after first-variance filtering / first-dispersion input amount] × 100) (ex) recovery rate% = [A / 1264] × 100)
1차 밀링 분 회수율을 100%로 하여 불소계 수지 LF-200 566g, 크실렌 170g을 혼합하여 총량을 2,000g으로 만들었다. 이때 무기입자와 바인더의 비율은 0.90이며 전체 고형분은 55.4 중량 %인 코팅 조성물을 얻을 수 있었다.566 g of fluorine-based resin LF-200 and 170 g of xylene were mixed with a primary milling fraction recovery rate of 100% to make the total amount 2,000 g. At this time, the ratio of the inorganic particles and the binder was 0.90, and the total solid content was 55.4% by weight.
상기 코팅 조성물을 기재층(PET Film, 188㎛)에 콤마 코터를 사용하여 습한상태에서의 코팅 두께를 40~50㎛로 하여 코팅한 후 1차건조로 120℃, 30분간 건조하고, 본 건조로 200℃, 10분간 건조하였다. 코팅된 기재층의 반대 면도 같은 방법으로 코팅하였다.The coating composition was coated on a base layer (PET Film, 188㎛) using a comma coater in a wet coating thickness of 40-50㎛, and then dried at 120 ° C. for 30 minutes by primary drying, followed by main drying It dried at 200 degreeC for 10 minutes. The coating was applied in the same manner as the opposite shaving of the coated substrate layer.
제조된 백시트 (판상 알루미나 함유 불소수지층/PET/판상 알루미나 함유 불소수지층)의 흡습성을 확인한 결과를 하기 표 1에 나타내었다.
Table 1 shows the results of confirming the hygroscopicity of the prepared backsheet (plate-like alumina-containing fluorine resin layer / PET / plate-like alumina-containing fluorine resin layer).
[실시예 2] [Example 2]
불소계 수지로 Lumifron LF-200(Asahi Glass, Solvent soluble Fluoropolymer, 고형분 60중량%) 404g, 판상 하이드로 탈사이트(SG-HT200F, SukgyungAT) 526g, 크실렌 334g을 플레니터리 믹서(NETESCH)를 사용하여 혼합하였다.As a fluorine-based resin, 404 g of Lumifron LF-200 (Asahi Glass, Solvent soluble Fluoropolymer, 60 wt% solids), 526 g of plate hydrotalcite (SG-HT200F, SukgyungAT), and 334 g of xylene were mixed using a planetary mixer (NETESCH). .
상기 혼합된 슬러리를 3-롤 밀(EXAKT)을 사용하여 밀링하여 균일하게 혼합한 후 20㎛ 마이크로 필터로 여과한 후 회수율을 계산하였다. (회수율 = [1차분산 필터링 후 회수량 /1차분산 투입량]×100) (ex) 회수율 % = [A/1264]×100)The mixed slurry was milled using a three-roll mill (EXAKT), uniformly mixed, filtered with a 20 μm micro filter, and then the recovery was calculated. (Recovery rate = [recovery amount after first-variance filtering / first-dispersion input amount] × 100) (ex) recovery rate% = [A / 1264] × 100)
1차 밀링 분 회수율을 100%로 하여 불소계 수지 LF-200 566g, 크실렌 170g을 혼합하여 총량을 2,000g으로 만들었다. 이때 무기입자와 바인더의 비율은 0.90이며 전체 고형분은 55.4 중량 %인 코팅 조성물을 얻을 수 있었다.566 g of fluorine-based resin LF-200 and 170 g of xylene were mixed with a primary milling fraction recovery rate of 100% to make the total amount 2,000 g. At this time, the ratio of the inorganic particles and the binder was 0.90, and the total solid content was 55.4% by weight.
상기 코팅 조성물을 기재층(PET Film, 188㎛)에 콤마 코터를 사용하여 습한상태에서의 코팅 두께를 40~50㎛로 코팅한 후 1차건조로 120℃, 30분 건조하고, 본 건조로 200℃, 10분간 건조하였다. 코팅된 기재층의 반대 면도 같은 방법으로 코팅 하였다.The coating composition was coated on a substrate layer (PET Film, 188㎛) using a comma coater in a wet coating thickness of 40-50㎛, and then dried at 120 ° C. for 30 minutes by primary drying, followed by 200 It dried at 10 degreeC. The coating was applied in the same manner as the opposite shaving of the coated substrate layer.
제조된 백시트(판상 하이드로 탈사이트 함유 불소수지층/PET/판상 하이드로 탈사이트 함유 불소수지층)의 흡습성을 확인한 결과를 하기 표 1에 나타내었다.
Table 1 shows the results of confirming the hygroscopicity of the prepared backsheet (plate hydrotalcite-containing fluorine resin layer / PET / plate hydrotalcite-containing fluorine resin layer).
[실시예 3] [Example 3]
불소계 수지로 Lumifron LF-200(Asahi Glass, Solvent soluble Fluoropolymer, 고형분 60중량%) 404g, 판상 알루미나(SG-FALO2000, SukgyungAT) 315.6g, 구형 티타니아(도 2, SG-TO200, SukgyungAT) 210.4g, 크실렌 334g을 플레니터리 믹서(NETESCH)를 사용하여 혼합하였다.Lumifron LF-200 (Asahi Glass, Solvent soluble Fluoropolymer, solid content 60% by weight) 404g, fluorine-based alumina (SG-FALO2000, SukgyungAT) 315.6g, spherical titania (Fig. 2, SG-TO200, SukgyungAT) 210.4g, Xylene 334 g was mixed using a planetary mixer (NETESCH).
상기 혼합된 슬러리를 3-롤 밀(EXAKT)을 사용하여 밀링하여 균일하게 혼합한 후 20㎛ 마이크로 필터로 여과한 후 회수율을 계산하였다. (회수율 = [1차분산 필터링 후 회수량 /1차분산 투입량]×100) (ex) 회수율 % = [A/1264]×100)The mixed slurry was milled using a three-roll mill (EXAKT), uniformly mixed, filtered with a 20 μm micro filter, and then the recovery was calculated. (Recovery rate = [recovery amount after first-variance filtering / first-dispersion input amount] × 100) (ex) recovery rate% = [A / 1264] × 100)
1차 밀링 분 회수율을 100%로 하여 불소계 수지 LF-200 566g, 크실렌 170g을 혼합하여 총량을 2,000g으로 만들었다. 이때 무기입자와 바인더의 비율은 0.90이며 전체 고형분은 55.4 중량 %인 코팅 조성물을 얻을 수 있었다.566 g of fluorine-based resin LF-200 and 170 g of xylene were mixed with a primary milling fraction recovery rate of 100% to make the total amount 2,000 g. At this time, the ratio of the inorganic particles and the binder was 0.90, and the total solid content was 55.4% by weight.
상기 코팅 조성물을 기재층(PET Film, 188㎛)에 콤마 코터를 사용하여 습한상태에서의 코팅 두께를 40~50㎛로 코팅한 후 1차건조로 120℃, 30분 건조하고, 본 건조로 200℃, 10분간 건조하였다. 코팅된 기재층의 반대 면도 같은 방법으로 코팅 하였다.The coating composition was coated on a substrate layer (PET Film, 188㎛) using a comma coater in a wet coating thickness of 40-50㎛, and then dried at 120 ° C. for 30 minutes by primary drying, followed by 200 It dried at 10 degreeC. The coating was applied in the same manner as the opposite shaving of the coated substrate layer.
제조된 백시트(판상 알루미나 및 구형 티타니아 함유 불소수지층/PET/판상 알루미나 및 구형 티타니아 함유 불소수지층)의 흡습성을 확인한 결과를 하기 표 1에 나타내었다.
Table 1 shows the results of confirming the hygroscopicity of the prepared backsheet (plate-like alumina and spherical titania-containing fluorine resin layer / PET / plate-like alumina and spherical titania-containing fluorine resin layer).
[실시예 4] Example 4
불소계 수지로 Lumifron LF-200(Asahi Glass, Solvent soluble Fluoropolymer, 고형분 60중량%) 404g, 판상 하이드로 탈사이트(SG-HT200F, SukgyungAT) 315.6g, 구형 티타니아(SG-TO200, SukgyungAT) 210.4g, 크실렌 334g을 플레니터리 믹서(NETESCH)를 사용하여 혼합하였다.Lumifron LF-200 (Asahi Glass, Solvent soluble Fluoropolymer, Solid content 60% by weight) 404g, Fluorinated Resin (SG-HT200F, SukgyungAT) 315.6g, Old Titania (SG-TO200, SukgyungAT) 210.4g, Xylene 334g Was mixed using a planetary mixer (NETESCH).
상기 혼합된 슬러리를 3-롤 밀(EXAKT)을 사용하여 밀링하여 균일하게 혼합한 후 20㎛ 마이크로 필터로 여과한 후 회수율을 계산하였다. (회수율 = [1차분산 필터링 후 회수량 /1차분산 투입량]×100) (ex) 회수율 % = [A/1264]×100)The mixed slurry was milled using a three-roll mill (EXAKT), uniformly mixed, filtered with a 20 μm micro filter, and then the recovery was calculated. (Recovery rate = [recovery amount after first-variance filtering / first-dispersion input amount] × 100) (ex) recovery rate% = [A / 1264] × 100)
1차 밀링 분 회수율을 100%로 하여 불소계 수지 LF-200 566g, 크실렌 170g을 혼합하여 총량을 2,000g으로 만들었다. 이때 무기입자와 바인더의 비율은 0.90이며 전체 고형분은 55.4 중량 %인 코팅 조성물을 얻을 수 있었다.566 g of fluorine-based resin LF-200 and 170 g of xylene were mixed with a primary milling fraction recovery rate of 100% to make the total amount 2,000 g. At this time, the ratio of the inorganic particles and the binder was 0.90, and the total solid content was 55.4% by weight.
상기 코팅 조성물을 기재층(PET Film, 188㎛)에 콤마 코터를 사용하여 습한상태에서의 코팅 두께를 40~50㎛로 코팅한 후 1차건조로 120℃, 30분 건조하고, 본 건조로 200℃, 10분간 건조하였다. 코팅된 기재층의 반대 면도 같은 방법으로 코팅 하였다.The coating composition was coated on a substrate layer (PET Film, 188㎛) using a comma coater in a wet coating thickness of 40-50㎛, and then dried at 120 ° C. for 30 minutes by primary drying, followed by 200 It dried at 10 degreeC. The coating was applied in the same manner as the opposite shaving of the coated substrate layer.
제조된 백시트(판상 하이드로 탈사이트 및 구형 티타니아 함유 불소수지층/PET/판상 하이드로 탈사이트 및 구형 티타니아 함유 불소수지층)의 흡습성을 확인한 결과를 하기 표 1에 나타내었다.
Table 1 shows the results of confirming the hygroscopicity of the prepared backsheet (plate hydrotalcite and spherical titania-containing fluorine resin layer / PET / plate hydrotalcite and spherical titania-containing fluorine resin layer).
[비교예 1]Comparative Example 1
불소계 수지 LF-200 800g, 크실렌 200g을 혼합한 후 상기 코팅 조성물을 기재층(PET Film, 188㎛)에 콤마 코터를 사용하여 습한상태에서 코팅 두께를 40~50㎛로 코팅한 후 1차건조로 120℃, 30분 건조하고, 본 건조로 200℃, 10분간 건조하였다. 코팅된 기재층의 반대 면도 같은 방법으로 코팅하였다.After mixing 800g of fluorine-based resin LF-200 and 200g of xylene, the coating composition was coated with a comma coater on a base layer (PET Film, 188㎛) in a wet state with a coating thickness of 40-50㎛, followed by primary drying. It dried at 120 degreeC for 30 minutes, and dried at 200 degreeC for 10 minutes by this drying. The coating was applied in the same manner as the opposite shaving of the coated substrate layer.
제조된 백시트(불소수지층/PET/불소수지층)의 흡습성을 확인한 결과를 하기 표 1에 나타내었다.
Table 1 shows the results of confirming the hygroscopicity of the prepared backsheet (fluorine resin layer / PET / fluorine resin layer).
[비교예 2]Comparative Example 2
실시예 1에서, 판상 알루미나 대신에, 1~3㎛의 용융 알루미나(Fused Alumina)를 사용한 것 이외에는 동일한 방법에 의해 필름을 제조하였다.In Example 1, the film was manufactured by the same method except having used fused alumina of 1-3 micrometers instead of plate-shaped alumina.
제조된 백시트(용융 알루미나 함유 불소수지층/PET/용융 알루미나 함유 불소수지층)의 흡습성을 확인한 결과를 하기 표 1에 나타내었다.Table 1 shows the results of confirming the hygroscopicity of the prepared backsheet (molten alumina-containing fluorine resin layer / PET / molten alumina-containing fluorine resin layer).
상기 WVTR(Water vapor transmission rate) 특성은 Illinois Instrument사의 7002 Water vapor Transmission Analyzer를 사용하여 샘플사이즈를 10cm×10cm로 하고 균일한 두께를 갖는 조건에서 측정하였다.
The water vapor transmission rate (WVTR) characteristics were measured under conditions having a uniform thickness with a sample size of 10 cm × 10 cm using an Illinois Instrument 7002 water vapor transmission analyzer.
상기와 같이, 본 발명의 바람직한 실시 예를 참조하여 설명하였지만 해당 기술 분야의 숙련된 당업자라면 하기의 특허청구범위에 기재된 본 발명의 사상 및 영역으로부터 벗어나지 않는 범위 내에서 본 발명을 다양하게 수정 및 변경시킬 수 있음을 이해할 수 있을 것이다.While the present invention has been particularly shown and described with reference to exemplary embodiments thereof, it will be understood by those skilled in the art that various changes and modifications may be made without departing from the spirit and scope of the invention as defined in the appended claims. It can be understood that
Claims (15)
상기 기재의 양면 또는 일면에 코팅된 판상입자 또는 층상형 규산염 화합물를 함유하며, 표면거칠기가 0.3~5.0㎛인 수지코팅층
을 포함하는 태양전지모듈용 백시트.materials; And
Resin coating layer containing plate-like particles or layered silicate compound coated on both or one side of the substrate, the surface roughness of 0.3 ~ 5.0㎛
Back sheet for a solar cell module comprising a.
기재는 폴리에스테르테레프탈레이트(PET) 필름인 것을 특징으로 하는 태양전지모듈용 백시트. 6. The method of claim 5,
The substrate is a polyester terephthalate (PET) film, characterized in that the solar cell module back sheet.
판상입자는 판상 알루미나 또는 판상 하이드로 탈사이트인 것을 특징으로 하는 태양전지모듈용 백시트.6. The method of claim 5,
The plate particle is a solar cell module back sheet, characterized in that the plate-shaped alumina or plate-like hydrotalcite.
판상입자는 장축대 단축의 비(Aspect ratio)가 5~300인 것을 특징으로 하는 태양전지모듈용 백시트.6. The method of claim 5,
The plate-shaped particle is a back sheet for a solar cell module, characterized in that the aspect ratio of the axis short axis (5 ~ 300).
판상입자는 장축이 0.2~30㎛, 단축이 0.01~5㎛인 것을 특징으로 하는 태양전지모듈용 백시트.6. The method of claim 5,
The plate-shaped particle is a back sheet for a solar cell module, characterized in that the major axis is 0.2 ~ 30㎛, the minor axis is 0.01 ~ 5㎛.
수지코팅층의 상면에 프라이머층이 더 형성된 것을 특징으로 하는 태양전지모듈용 백시트.6. The method of claim 5,
The solar cell module back sheet, characterized in that the primer layer is further formed on the upper surface of the resin coating layer.
판상입자 또는 층상형 규산염 화합물은 수지 중량에 대하여 1~50 중량% 포함된 것을 특징으로 하는 태양전지모듈용 백시트.6. The method of claim 5,
Plate-like particles or layered silicate compound is a solar cell module back sheet, characterized in that contained 1 to 50% by weight based on the weight of the resin.
A solar cell module comprising the backsheet of claim 5.
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US20080264484A1 (en) * | 2007-02-16 | 2008-10-30 | Marina Temchenko | Backing sheet for photovoltaic modules and method for repairing same |
KR101022820B1 (en) | 2009-03-23 | 2011-03-17 | 이정민 | Back sheet for module, its manufacturing method and its manufacturing apparatus thereof |
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KR101022820B1 (en) | 2009-03-23 | 2011-03-17 | 이정민 | Back sheet for module, its manufacturing method and its manufacturing apparatus thereof |
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