CN114686055A - A fluorocarbon coating solution, a fluorocarbon coating, and a solar back panel - Google Patents
A fluorocarbon coating solution, a fluorocarbon coating, and a solar back panel Download PDFInfo
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- CN114686055A CN114686055A CN202011578668.6A CN202011578668A CN114686055A CN 114686055 A CN114686055 A CN 114686055A CN 202011578668 A CN202011578668 A CN 202011578668A CN 114686055 A CN114686055 A CN 114686055A
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- NBVXSUQYWXRMNV-UHFFFAOYSA-N fluoromethane Chemical compound FC NBVXSUQYWXRMNV-UHFFFAOYSA-N 0.000 title claims abstract description 173
- 238000000576 coating method Methods 0.000 title claims abstract description 151
- 239000011248 coating agent Substances 0.000 title claims abstract description 135
- 229920005989 resin Polymers 0.000 claims abstract description 60
- 239000011347 resin Substances 0.000 claims abstract description 60
- 239000012948 isocyanate Substances 0.000 claims abstract description 54
- 150000002513 isocyanates Chemical class 0.000 claims abstract description 54
- 239000000843 powder Substances 0.000 claims abstract description 41
- 229910000422 cerium(IV) oxide Inorganic materials 0.000 claims abstract description 36
- CETPSERCERDGAM-UHFFFAOYSA-N ceric oxide Chemical compound O=[Ce]=O CETPSERCERDGAM-UHFFFAOYSA-N 0.000 claims abstract description 34
- 239000007788 liquid Substances 0.000 claims abstract description 30
- 239000000654 additive Substances 0.000 claims abstract description 22
- 230000000996 additive effect Effects 0.000 claims abstract description 22
- 239000002318 adhesion promoter Substances 0.000 claims abstract description 11
- 239000002250 absorbent Substances 0.000 claims abstract description 5
- 230000002745 absorbent Effects 0.000 claims abstract description 4
- 239000006096 absorbing agent Substances 0.000 claims description 40
- 229920000058 polyacrylate Polymers 0.000 claims description 37
- 229920002803 thermoplastic polyurethane Polymers 0.000 claims description 37
- 229920001343 polytetrafluoroethylene Polymers 0.000 claims description 31
- 239000004810 polytetrafluoroethylene Substances 0.000 claims description 31
- 239000004433 Thermoplastic polyurethane Substances 0.000 claims description 29
- 239000010410 layer Substances 0.000 claims description 28
- -1 polytetrafluoroethylene Polymers 0.000 claims description 28
- 239000002245 particle Substances 0.000 claims description 23
- 239000007787 solid Substances 0.000 claims description 20
- 229920000642 polymer Polymers 0.000 claims description 15
- 239000013638 trimer Substances 0.000 claims description 15
- 239000000463 material Substances 0.000 claims description 13
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 claims description 12
- 229910052731 fluorine Inorganic materials 0.000 claims description 12
- 239000011737 fluorine Substances 0.000 claims description 12
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical group O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 10
- 239000012790 adhesive layer Substances 0.000 claims description 10
- 239000002033 PVDF binder Substances 0.000 claims description 6
- 229920002620 polyvinyl fluoride Polymers 0.000 claims description 6
- 229920002981 polyvinylidene fluoride Polymers 0.000 claims description 6
- 239000005057 Hexamethylene diisocyanate Substances 0.000 claims description 5
- 239000005058 Isophorone diisocyanate Substances 0.000 claims description 5
- 239000002253 acid Substances 0.000 claims description 5
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 claims description 5
- NIMLQBUJDJZYEJ-UHFFFAOYSA-N isophorone diisocyanate Chemical compound CC1(C)CC(N=C=O)CC(C)(CN=C=O)C1 NIMLQBUJDJZYEJ-UHFFFAOYSA-N 0.000 claims description 5
- 239000002105 nanoparticle Substances 0.000 claims description 5
- 229920002493 poly(chlorotrifluoroethylene) Polymers 0.000 claims description 5
- 239000005023 polychlorotrifluoroethylene (PCTFE) polymer Substances 0.000 claims description 5
- DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical group CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 claims description 5
- 239000012752 auxiliary agent Substances 0.000 claims description 4
- 239000000377 silicon dioxide Substances 0.000 claims description 4
- 235000012239 silicon dioxide Nutrition 0.000 claims description 4
- 150000002148 esters Chemical class 0.000 claims description 2
- BWVAOONFBYYRHY-UHFFFAOYSA-N [4-(hydroxymethyl)phenyl]methanol Chemical compound OCC1=CC=C(CO)C=C1 BWVAOONFBYYRHY-UHFFFAOYSA-N 0.000 claims 1
- 239000003292 glue Substances 0.000 claims 1
- 229920000052 poly(p-xylylene) Polymers 0.000 claims 1
- 238000012360 testing method Methods 0.000 abstract description 26
- 238000000034 method Methods 0.000 abstract description 10
- 230000008569 process Effects 0.000 abstract description 9
- 229920002521 macromolecule Polymers 0.000 abstract description 2
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- 239000003960 organic solvent Substances 0.000 description 27
- 239000000758 substrate Substances 0.000 description 22
- 229920000139 polyethylene terephthalate Polymers 0.000 description 19
- 239000005020 polyethylene terephthalate Substances 0.000 description 19
- 238000002360 preparation method Methods 0.000 description 17
- DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 14
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 14
- 238000011056 performance test Methods 0.000 description 13
- 230000000052 comparative effect Effects 0.000 description 12
- 229910000420 cerium oxide Inorganic materials 0.000 description 11
- 230000032683 aging Effects 0.000 description 10
- 230000000694 effects Effects 0.000 description 9
- 238000005538 encapsulation Methods 0.000 description 7
- BMMGVYCKOGBVEV-UHFFFAOYSA-N oxo(oxoceriooxy)cerium Chemical compound [Ce]=O.O=[Ce]=O BMMGVYCKOGBVEV-UHFFFAOYSA-N 0.000 description 7
- 230000008901 benefit Effects 0.000 description 6
- 229910021419 crystalline silicon Inorganic materials 0.000 description 5
- 238000001035 drying Methods 0.000 description 5
- 238000002834 transmittance Methods 0.000 description 5
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- 230000001070 adhesive effect Effects 0.000 description 4
- 230000008859 change Effects 0.000 description 4
- 238000001723 curing Methods 0.000 description 4
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- 238000009413 insulation Methods 0.000 description 3
- 238000003475 lamination Methods 0.000 description 3
- 238000004806 packaging method and process Methods 0.000 description 3
- 238000010248 power generation Methods 0.000 description 3
- 150000003384 small molecules Chemical class 0.000 description 3
- 238000004383 yellowing Methods 0.000 description 3
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 2
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 2
- QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical compound C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 description 2
- 239000012964 benzotriazole Substances 0.000 description 2
- 230000015556 catabolic process Effects 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
- 238000006731 degradation reaction Methods 0.000 description 2
- 239000003973 paint Substances 0.000 description 2
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- 229910052710 silicon Inorganic materials 0.000 description 2
- 239000010703 silicon Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 238000010998 test method Methods 0.000 description 2
- 238000001029 thermal curing Methods 0.000 description 2
- 235000012431 wafers Nutrition 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 1
- 230000006750 UV protection Effects 0.000 description 1
- 238000009825 accumulation Methods 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 230000003679 aging effect Effects 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000008199 coating composition Substances 0.000 description 1
- 238000007872 degassing Methods 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 230000018109 developmental process Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 238000010030 laminating Methods 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
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- 230000001737 promoting effect Effects 0.000 description 1
- 230000004224 protection Effects 0.000 description 1
- 238000000197 pyrolysis Methods 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- 239000006097 ultraviolet radiation absorber Substances 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
- C09D127/00—Coating compositions 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 a halogen; Coating compositions based on derivatives of such polymers
- C09D127/02—Coating compositions 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 a halogen; Coating compositions based on derivatives of such polymers not modified by chemical after-treatment
- C09D127/12—Coating compositions 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 a halogen; Coating compositions based on derivatives of such polymers not modified by chemical after-treatment containing fluorine atoms
- C09D127/18—Homopolymers or copolymers of tetrafluoroethene
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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
- C09D7/42—Gloss-reducing agents
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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
- C09D7/48—Stabilisers against degradation by oxygen, light or heat
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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
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- 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
- C09D7/67—Particle size smaller than 100 nm
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- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10F—INORGANIC SEMICONDUCTOR DEVICES SENSITIVE TO INFRARED RADIATION, LIGHT, ELECTROMAGNETIC RADIATION OF SHORTER WAVELENGTH OR CORPUSCULAR RADIATION
- H10F19/00—Integrated devices, or assemblies of multiple devices, comprising at least one photovoltaic cell covered by group H10F10/00, e.g. photovoltaic modules
- H10F19/80—Encapsulations or containers for integrated devices, or assemblies of multiple devices, having photovoltaic cells
- H10F19/85—Protective back sheets
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Abstract
Description
技术领域technical field
本发明涉及太阳能背板技术领域,具体而言,涉及一种氟碳涂布液及一种氟碳涂层、及一种太阳能背板。The invention relates to the technical field of solar back sheets, in particular to a fluorocarbon coating solution, a fluorocarbon coating, and a solar back sheet.
背景技术Background technique
为了解决光伏组件发电功率问题,目前的硅片电池尺寸已经从传统的163mm,166mm向182mm,210mm大尺寸转变。伴随着整体组件功率的提升,对传统背板提出了更严格的需求。而透明组件的开发应用,更加对组件功率提升具备了不可磨灭的贡献。与传统组件相比,透明大尺寸组件功率已经超过550W,发电过程中电流热效应已经成为不可避免的事实。In order to solve the power generation problem of photovoltaic modules, the current size of silicon wafer cells has changed from the traditional 163mm, 166mm to 182mm, 210mm large size. Along with the increase in overall component power, more stringent demands are placed on traditional backplanes. The development and application of transparent components has made an indelible contribution to the improvement of component power. Compared with traditional modules, the power of transparent large-scale modules has exceeded 550W, and the current heating effect in the power generation process has become an inevitable fact.
由于高电流引起的热效应,在光伏组件中可以用热斑效应来模拟。大组件的热斑温度已经超过了170℃,比传统的组件偏高20℃以上。这种高温对背面封装材料背板提出了更高的耐热需求。一般的透明氟碳配方中添加的小分子在这种温度下就面临着析出、降解等风险。Due to the thermal effect caused by high current, it can be simulated by the hot spot effect in photovoltaic modules. The hot spot temperature of large modules has exceeded 170°C, which is more than 20°C higher than that of traditional modules. This high temperature places higher thermal demands on the backside encapsulation material backplane. Small molecules added in general transparent fluorocarbon formulations face the risk of precipitation and degradation at this temperature.
发明内容SUMMARY OF THE INVENTION
为了解决透明氟碳涂层的耐热性差的问题,本发明提供一种氟碳涂布液及一种氟碳涂层、及一种太阳能背板。该氟碳涂布液形成的涂层在热斑温度(例如170℃)下的耐热性好,外观无明显变化,表示不易发生小分子析出、和大分子的降解,在组件热封后进行高温热斑测试过程中不会发生涂层的发黄。In order to solve the problem of poor heat resistance of the transparent fluorocarbon coating, the present invention provides a fluorocarbon coating solution, a fluorocarbon coating, and a solar back sheet. The coating formed by the fluorocarbon coating solution has good heat resistance at the hot spot temperature (for example, 170°C), and there is no obvious change in appearance, indicating that the precipitation of small molecules and the degradation of macromolecules are not easy to occur. No yellowing of the coating occurs during the high temperature hot spot test.
进一步的,为了解决目前光伏组件增大后带来的热效应问题,本发明提供一种氟碳涂布液及一种氟碳涂层、及一种太阳能背板。所述氟碳涂层是一种无机纳米氧化铈的紫外吸收剂涂层。与现有技术相比,本发明提供的方案在耐热性上具有足够稳定的优势,对比传统的有机UV吸收剂,涂层在热斑测试过程中不会发生消耗或者损坏。所以合理的选择更具有稳定性的无机纳米UV吸收剂,对透明涂料的耐热性能提升,具有深远意义。Further, in order to solve the problem of thermal effect caused by the enlargement of the current photovoltaic modules, the present invention provides a fluorocarbon coating solution, a fluorocarbon coating, and a solar back sheet. The fluorocarbon coating is an ultraviolet absorber coating of inorganic nano-cerium oxide. Compared with the prior art, the solution provided by the present invention has the advantage of being sufficiently stable in heat resistance, and compared with the traditional organic UV absorber, the coating will not be consumed or damaged during the hot spot test. Therefore, the reasonable selection of more stable inorganic nano UV absorbers has far-reaching significance for improving the heat resistance of transparent coatings.
本发明提供一种氟碳涂布液,所述氟碳涂布液按照重量百分比计包含50%~80%的氟碳树脂,3%~10%的无机纳米二氧化铈UV吸收剂,1%~5%的消光粉,10%~20%的附着力促进剂,0.3%~0.8%的添加剂,5%~20%的异氰酸酯。The invention provides a fluorocarbon coating solution, which comprises 50%-80% by weight of fluorocarbon resin, 3%-10% of inorganic nano-cerium dioxide UV absorber, 1% by weight ~5% Matting Powder, 10%~20% Adhesion Promoter, 0.3%~0.8% Additive, 5%~20% Isocyanate.
进一步的,所述无机二氧化铈纳米粒子的粒径为10~30nm。Further, the particle size of the inorganic ceria nanoparticles is 10-30 nm.
进一步的,所述氟碳涂布液还包括有机溶剂,固含量为50%~70%。Further, the fluorocarbon coating solution further includes an organic solvent, and the solid content is 50% to 70%.
所述氟碳涂布液又称为氟碳涂料。The fluorocarbon coating liquid is also called fluorocarbon coating.
将氟碳涂布液的配比限定在上述范围内,对熟化完成后在透明层上的附着力优异,并且满足封装强度要求,同时因为采用了无机纳米吸收剂,在高温状态下不易发生分解,进而可以提升整体组件的抗热斑性能。The ratio of the fluorocarbon coating liquid is limited to the above range, which has excellent adhesion on the transparent layer after curing, and meets the requirements of packaging strength. At the same time, due to the use of inorganic nano-absorbents, it is not easy to decompose at high temperatures. , thereby improving the hot spot resistance of the overall assembly.
进一步的,所述氟碳涂布液的固含量优选为58%~65%。Further, the solid content of the fluorocarbon coating liquid is preferably 58% to 65%.
将上述氟碳涂布液固含量限定在该范围,有利于氟碳层均匀的涂布在基材表面。The solid content of the fluorocarbon coating solution is limited to this range, which is beneficial to the uniform coating of the fluorocarbon layer on the surface of the substrate.
进一步的,所述氟碳树脂可以是聚偏氟乙烯、聚氟乙烯、聚四氟乙烯、聚三氟氯乙烯、聚六氟丙烯中的一种或多种。Further, the fluorocarbon resin may be one or more of polyvinylidene fluoride, polyvinyl fluoride, polytetrafluoroethylene, polychlorotrifluoroethylene, and polyhexafluoropropylene.
所述氟碳树脂利用氟碳键高键能的特点,可以实现耐候性的特点。The fluorocarbon resin utilizes the characteristics of high bond energy of fluorocarbon bonds, and can achieve the characteristics of weather resistance.
进一步的,所述氟碳树脂是热固化型树脂。Further, the fluorocarbon resin is a thermosetting resin.
所述氟碳树脂由大金氟化工提供。The fluorocarbon resin was provided by Daikin Fluorochemical.
进一步的,所述的UV吸收剂是无机二氧化铈纳米分子,粒径在10~30nm。Further, the UV absorber is an inorganic ceria nano-molecule with a particle size of 10-30 nm.
一般有机UV吸收剂热稳定性有限,现在组件功率越做越大,强电流下热量越来越高。组件有个标准叫热斑温度,以前一般组件热斑温度只有130-140,现在大尺寸组件可以达到170-180。本发明利用了氧化铈这个无机UV吸收剂,相比有机UV吸收剂,氧化铈具有长期稳定性,尤其是高温稳定性优势。氧化铈UV吸收剂是用在透明组件中,目前高功率的光伏电池都是双面发电组件,必须使用透明的背板。而透明背板要求合适的透光率,大粒径的UV吸收剂会造成透光率下降,但是太小的粒子在涂布过程中容易团聚,性能也不稳定,所以无机二氧化铈纳米分子的粒径为10~30nm。Generally, the thermal stability of organic UV absorbers is limited. Now the power of the components is getting bigger and bigger, and the heat is getting higher and higher under the strong current. There is a standard for modules called hot spot temperature. In the past, the hot spot temperature of general modules was only 130-140, and now large-sized modules can reach 170-180. The present invention utilizes cerium oxide as an inorganic UV absorber. Compared with organic UV absorbers, cerium oxide has the advantage of long-term stability, especially high temperature stability. Cerium oxide UV absorbers are used in transparent modules. At present, high-power photovoltaic cells are double-sided power generation modules, and a transparent backsheet must be used. The transparent backplane requires a suitable light transmittance. Large particle size UV absorbers will cause a decrease in light transmittance, but too small particles are easy to agglomerate during the coating process, and their performance is also unstable. Therefore, inorganic ceria nano-molecules The particle size is 10 to 30 nm.
进一步的,所述的消光粉是二氧化硅粒子。Further, the matting powder is silica particles.
进一步的,所述二氧化硅粒子是格雷斯提供的。Further, the silica particles are provided by Grace.
进一步的,添加的助剂是用于改性氟碳树脂的,添加类型是聚丙烯酸酯类型的。Further, the added auxiliary is used to modify the fluorocarbon resin, and the added type is polyacrylate type.
所述的聚丙烯酸酯类型主要用于调控氟碳涂料的耐候性后的粘接力。The polyacrylate type described is mainly used to adjust the adhesive force after the weather resistance of the fluorocarbon coating.
所述聚丙烯酸酯是毕克化学提供的。The polyacrylate was supplied by BYK.
进一步的,所述的附着力促进树脂是热塑性聚氨酯树脂。Further, the adhesion promoting resin is thermoplastic polyurethane resin.
所述的热塑性聚氨酯树脂是禾大化学提供的。The thermoplastic polyurethane resin is provided by Croda Chemical.
进一步的,所述的固化剂种类是异氰酸酯类型的。Further, the type of curing agent is of isocyanate type.
进一步的,所述的异氰酸酯可以是甲苯二异氰酸酯三聚体或多聚体,六亚甲基二异氰酸酯三聚体或多聚体,异氟尔酮二异氰酸酯三聚体或多聚体。Further, the isocyanate can be a trimer or polymer of toluene diisocyanate, a trimer or polymer of hexamethylene diisocyanate, and a trimer or polymer of isophorone diisocyanate.
进一步的,所述的异氰酸酯是拜耳公司提供的。Further, the isocyanate is provided by Bayer.
进一步的,所述氟碳树脂选自聚偏氟乙烯、聚氟乙烯、聚四氟乙烯、聚三氟氯乙烯、聚六氟丙烯中的一种或多种;所述消光粉为二氧化硅;所述附着力促进剂是低酸值的热塑性聚氨酯树脂;所述的添加剂是聚丙烯酸酯类助剂;,所述的异氰酸酯选自甲苯二异氰酸酯三聚体或多聚体,六亚甲基二异氰酸酯三聚体或多聚体,或异氟尔酮二异氰酸酯三聚体或多聚体。Further, the fluorocarbon resin is selected from one or more of polyvinylidene fluoride, polyvinyl fluoride, polytetrafluoroethylene, polychlorotrifluoroethylene, and polyhexafluoropropylene; the matting powder is silicon dioxide ; Described adhesion promoter is thermoplastic polyurethane resin with low acid value; Described additive is polyacrylate auxiliary agent; Described isocyanate is selected from toluene diisocyanate trimer or polymer, hexamethylene Diisocyanate trimers or polymers, or isophorone diisocyanate trimers or polymers.
所述有机溶剂选自乙酸乙酯,乙酸丁酯,丁酮,或环己酮中的一种或至少两种的组合。The organic solvent is selected from one or a combination of at least two of ethyl acetate, butyl acetate, butanone, or cyclohexanone.
进一步的,所述氟碳涂布液包含62%~70%的氟碳树脂,5~7%的纳米氧化铈,2%~3%消光粉,0.4%~0.5%的聚丙烯酸酯,12%-14.6%的热塑性聚氨酯树脂,9.5%~13.6%的异氰酸酯,控制固含量在58%~65%。上述技术方案包括实施例1、4、5。Further, the fluorocarbon coating solution contains 62%-70% of fluorocarbon resin, 5-7% of nano-cerium oxide, 2%-3% of matting powder, 0.4%-0.5% of polyacrylate, 12% of -14.6% thermoplastic polyurethane resin, 9.5%~13.6% isocyanate, control solid content at 58%~65%. The above technical solutions include Embodiments 1, 4, and 5.
将氟碳涂料配方限定在上述优选参数范围内,可以保证该涂层具有高耐湿热老化性,并且在湿热老化后依旧可以保持高强度,而且在热斑测试条件下可以保持涂层的热稳定性。Limiting the fluorocarbon coating formulation within the above-mentioned preferred parameters can ensure that the coating has high resistance to damp heat aging, and can still maintain high strength after damp heat aging, and can maintain the thermal stability of the coating under hot spot test conditions. sex.
本发明还提供一种太阳能背板,所述太阳能背板依次包括透明氟碳涂层,基材,胶黏剂层,氟膜层。所述的透明氟碳涂层包括氟碳树脂、UV吸收剂、消光粉、聚丙烯酸酯、低酸值热塑性聚氨酯树脂、异氰酸酯等。The present invention also provides a solar back sheet, which sequentially comprises a transparent fluorocarbon coating, a base material, an adhesive layer, and a fluorine film layer. The transparent fluorocarbon coating includes fluorocarbon resin, UV absorber, matting powder, polyacrylate, low acid value thermoplastic polyurethane resin, isocyanate and the like.
进一步的,所述基材为透明的基材,所述基材层的材料选自聚对苯二甲基乙二醇酯(PET)。Further, the substrate is a transparent substrate, and the material of the substrate layer is selected from polyethylene terephthalate (PET).
进一步的,所述的胶黏剂是聚酯型胶黏剂。Further, the adhesive is a polyester adhesive.
进一步的,所述的氟膜是透明的PVF膜或PVDF膜。Further, the fluorine film is a transparent PVF film or PVDF film.
本发明提供一种氟碳涂层,所述氟碳涂层按照重量百分比计包含50%~80%的氟碳树脂,3%~10%的无机纳米二氧化铈UV吸收剂,1%~5%的消光粉,10%~20%的附着力促进剂,0.3%~0.8%的添加剂酯,5%~20%的异氰酸酯。进一步的,所述无机二氧化铈纳米粒子的粒径为10~30nm。进一步的,所述氟碳树脂选自聚偏氟乙烯、聚氟乙烯、聚四氟乙烯、聚三氟氯乙烯、聚六氟丙烯中的一种或多种;所述消光粉为二氧化硅;所述附着力促进剂是低酸值的热塑性聚氨酯树脂;所述的添加剂是聚丙烯酸酯类助剂;,所述的异氰酸酯选自甲苯二异氰酸酯三聚体或多聚体,六亚甲基二异氰酸酯三聚体或多聚体,或异氟尔酮二异氰酸酯三聚体或多聚体。The invention provides a fluorocarbon coating. The fluorocarbon coating comprises 50% to 80% of a fluorocarbon resin, 3% to 10% of an inorganic nano-cerium dioxide UV absorber, 1% to 5% by weight of the fluorocarbon coating. % of matting powder, 10% to 20% of adhesion promoter, 0.3% to 0.8% of additive ester, 5% to 20% of isocyanate. Further, the particle size of the inorganic ceria nanoparticles is 10-30 nm. Further, the fluorocarbon resin is selected from one or more of polyvinylidene fluoride, polyvinyl fluoride, polytetrafluoroethylene, polychlorotrifluoroethylene, and polyhexafluoropropylene; the matting powder is silicon dioxide ; Described adhesion promoter is thermoplastic polyurethane resin with low acid value; Described additive is polyacrylate auxiliary agent; Described isocyanate is selected from toluene diisocyanate trimer or polymer, hexamethylene Diisocyanate trimers or polymers, or isophorone diisocyanate trimers or polymers.
进一步的,在制备过程中,所述的氟碳涂层材料先配置成氟碳涂布液,按照重量百分比计包含按照50%~80%的氟碳树脂,3%~10%的无机纳米二氧化铈UV吸收剂,粒径在10~30nm,1%~5%的消光粉,10%~20%的热塑性聚氨酯附着力促进剂,0.3%~0.8%的聚丙烯酸酯,5%~20%的异氰酸酯,控制固含量在50%~70%。Further, in the preparation process, the fluorocarbon coating material is first configured into a fluorocarbon coating solution, which contains 50% to 80% of fluorocarbon resin and 3% to 10% of inorganic nano-dioxide according to the weight percentage. Cerium oxide UV absorber, particle size is 10~30nm, 1%~5% matting powder, 10%~20% thermoplastic polyurethane adhesion promoter, 0.3%~0.8% polyacrylate, 5%~20% isocyanate, the solid content is controlled at 50% to 70%.
进一步的,所述太阳能背板依次包括透明氟碳涂层、基材层、贴合胶层(也称为胶黏剂层)和氟膜层。Further, the solar back sheet sequentially includes a transparent fluorocarbon coating, a substrate layer, a bonding adhesive layer (also referred to as an adhesive layer) and a fluorine film layer.
进一步的,透明氟碳涂层的厚度为10~20μm;所述基材层的厚度为250~300μm,优选275~300μm;所述的胶黏剂层的厚度为6~10μm;所述的氟膜层的厚度为20~25μm。Further, the thickness of the transparent fluorocarbon coating is 10-20 μm; the thickness of the substrate layer is 250-300 μm, preferably 275-300 μm; the thickness of the adhesive layer is 6-10 μm; The thickness of the film layer is 20 to 25 μm.
进一步的,所述氟碳层的厚度优选为15~17μm。Further, the thickness of the fluorocarbon layer is preferably 15-17 μm.
本发明提供的透明太阳能背板可用于光伏组件的最外层背板封装材料。The transparent solar back sheet provided by the present invention can be used for the outermost back sheet encapsulation material of photovoltaic modules.
本发明提供的太阳能背板的制备方法包括以下步骤:The preparation method of the solar back sheet provided by the present invention comprises the following steps:
先将透明氟碳涂布液涂布在基材表面,放置在循环烘箱热固化处理,形成透明氟碳涂层(简称氟碳层);然后在基材另一面涂布胶黏剂层,放置在循环烘箱中干燥,贴合氟膜层;最后做一次熟化反应。First coat the transparent fluorocarbon coating solution on the surface of the substrate, and place it in a circulating oven for thermal curing to form a transparent fluorocarbon coating (referred to as fluorocarbon layer); then coat the other side of the substrate with an adhesive layer, place it on Dry in a circulating oven and attach the fluorine film layer; finally do a curing reaction.
进一步的,透明氟碳循环烘箱干燥的温度为150℃,时间为2分钟。Further, the drying temperature of the transparent fluorocarbon circulating oven is 150° C. and the time is 2 minutes.
进一步的,胶粘层的干燥温度为90℃,时间为2分钟。Further, the drying temperature of the adhesive layer was 90° C. and the time was 2 minutes.
进一步的,熟化反应温度为50℃,时间为48小时。Further, the aging reaction temperature was 50°C, and the time was 48 hours.
进一步的,基材为宁波勤邦提供的型号KP20基材。所述基材又称为PET基材。Further, the base material is the model KP20 base material provided by Ningbo Qinbang. The substrate is also referred to as a PET substrate.
上述涂布工艺、热熟化工艺、贴合工艺,可以根据现有技术进行设定。The above-mentioned coating process, thermal curing process, and laminating process can be set according to the prior art.
在将氟碳涂布液涂布在基材表面之前,上述制备方法还包括将原料配置成氟碳涂布液的步骤。Before coating the fluorocarbon coating liquid on the surface of the substrate, the above preparation method further includes the step of preparing the raw material into the fluorocarbon coating liquid.
本发明提供的氟碳涂布液中的氟碳树脂与纳米氧化铈对湿热、UV老化性有重要影响,添加的热塑胶聚氨酯对在透明PET表面附着力起到重要作用,添加的消光粉对涂料加工性能具有重要作用。The fluorocarbon resin and nano-cerium oxide in the fluorocarbon coating solution provided by the present invention have an important influence on damp heat and UV aging properties, the added thermoplastic polyurethane plays an important role in the adhesion on the surface of transparent PET, and the added matting powder Coating processability plays an important role.
本发明提供的氟碳涂层实现了如下技术效果:The fluorocarbon coating provided by the invention has achieved the following technical effects:
1.将上述氟碳涂布液固化成氟碳层后,可以实现耐老化、满足封装强度的太阳能背板内层材料。1. After the above-mentioned fluorocarbon coating liquid is cured into a fluorocarbon layer, the inner layer material of the solar back sheet that is resistant to aging and meets the encapsulation strength can be realized.
2.涂料中采用的氧化铈纳米粒子,在耐热斑测试过程中具有较好的稳定性,可以满足大功率组件的耐热性和户外使用效果。2. The cerium oxide nanoparticles used in the coating have good stability during the heat-spot test, which can meet the heat resistance and outdoor use effect of high-power components.
本发明提供的方案在耐热性上具有足够稳定的优势,氟碳涂层在热斑测试过程中不会发生消耗或者损坏。The solution provided by the present invention has the advantage of being sufficiently stable in heat resistance, and the fluorocarbon coating will not be consumed or damaged during the hot spot test.
附图说明Description of drawings
图1为本发明提供的太阳能背板的结构示意图。FIG. 1 is a schematic structural diagram of a solar back panel provided by the present invention.
具体实施方式Detailed ways
为了更易理解本发明的结构及所能达成的功能特征和优点,下文将本发明的较佳的实施例,并配合图式做详细说明如下:In order to more easily understand the structure of the present invention and the functional features and advantages that can be achieved, the preferred embodiments of the present invention are described below in detail with the drawings as follows:
如图1所示,所述太阳能背板结构包括透明氟碳涂层40,聚对苯二甲基乙二醇酯基材30,贴合胶层20以及氟膜层10。As shown in FIG. 1 , the solar back sheet structure includes a
(1)将透明氟碳涂布液涂布在基材表面,放置在循环烘箱固化处理,形成透明氟碳层;(2)将涂过氟碳层的半成品基材另一面涂布胶粘层,胶粘层放置在循环烘箱干燥处理,再复合氟膜层;(3)将太阳能背板成品熟化反应;(4)将太阳能背板的氟碳涂层与EVA层压制备模拟测试封装强度。(1) Coat the transparent fluorocarbon coating solution on the surface of the substrate, and place it in a circulating oven for curing to form a transparent fluorocarbon layer; (2) Coat the other side of the semi-finished substrate coated with the fluorocarbon layer with an adhesive layer , the adhesive layer is placed in a circulating oven for drying, and then the fluorine film layer is compounded; (3) the finished solar back sheet is cured; (4) the fluorocarbon coating of the solar back sheet is laminated with EVA to simulate and test the packaging strength.
进一步的,(1)过程中氟碳层处理的循环烘箱干燥的温度为150℃,时间为2分钟;Further, (1) in the process, the drying temperature of the circulating oven for the treatment of the fluorocarbon layer is 150° C., and the time is 2 minutes;
进一步的,(2)过程胶黏剂干燥的循环烘箱温度为90℃,时间为2分钟;Further, (2) the circulating oven temperature of the process adhesive drying is 90 ℃, and the time is 2 minutes;
进一步的,(3)过程的熟化处理温度为50℃,时间为48小时。Further, the aging treatment temperature in the process (3) was 50° C. and the time was 48 hours.
进一步的,(4)过程的层压参数建议为温度145℃,抽真空6分钟,放气30秒,层压压力0.1MPa,层压12分钟。Further, the lamination parameters of the process (4) are suggested as temperature 145°C, vacuuming for 6 minutes, degassing for 30 seconds, lamination pressure 0.1 MPa, and lamination for 12 minutes.
进一步的,选择的层压EVA是福斯特提供的F806。Further, the laminated EVA of choice is F806 supplied by Foster.
进一步的,选择的基材为宁波勤邦提供的型号KP20基材。所述基材又称为PET基材。Further, the selected base material is the model KP20 base material provided by Ningbo Qinbang. The substrate is also referred to as a PET substrate.
在将氟碳涂布液涂布在基材表面之前,上述制备方法还包括将氟碳层的原料配置成氟碳涂布液的步骤。Before coating the fluorocarbon coating solution on the surface of the substrate, the above preparation method further includes the step of configuring the raw material of the fluorocarbon layer into the fluorocarbon coating solution.
本发明提供的氟碳涂层进行下述测试:The fluorocarbon coating provided by the present invention carries out the following tests:
氟碳层的附着力:按照GB 1720-1979《漆膜附着力测定法》的标准,测试氟碳层对基材的附着力,其中100/100代表不脱膜,90/100代表脱落10%。Adhesion of fluorocarbon layer: According to the standard of GB 1720-1979 "Determination of Paint Film Adhesion", test the adhesion of fluorocarbon layer to the substrate, of which 100/100 means no peeling, 90/100 means 10% off .
封装强度测试:按照GB/T 31034-2014《晶体硅太阳能电池组件用绝缘背板》的标准,测试内氟碳层与EVA的粘接强度,采用180°剥离力测试方法进行。Encapsulation strength test: According to the standard of GB/T 31034-2014 "Insulating Backplane for Crystalline Silicon Solar Cell Modules", the bonding strength of the inner fluorocarbon layer and EVA is tested, using the 180° peel force test method.
QUV老化处理:按照GB/T 31034-2014《晶体硅太阳能电池组件用绝缘背板》的标准,用紫外老化灯处理,累积紫外能量达到120kwh/㎡,取出样品观察外观。QUV aging treatment: According to the standard of GB/T 31034-2014 "Insulation Backplane for Crystalline Silicon Solar Cell Modules", it is treated with an ultraviolet aging lamp, and the accumulated ultraviolet energy reaches 120kwh/㎡, and the sample is taken out to observe the appearance.
反射率:按照GB/T 31034-2014《晶体硅太阳能电池组件用绝缘背板》的标准进行反射率测试。Reflectivity: The reflectivity test is carried out according to the standard of GB/T 31034-2014 "Insulation Backsheet for Crystalline Silicon Solar Cell Modules".
湿热老化处理:按照GB/T 31034-2014《晶体硅太阳能电池组件用绝缘背板》的标准,在高温高湿箱体设置温度为85℃,湿度为85%,累积时间为2000h,取出样品观察外观并测试封装强度。测试封装强度后,观察氟碳涂层的外观,无黄变、无鼓包者为合格(即OK)(见表1中的热斑测试外观)。Damp heat aging treatment: According to the standard of GB/T 31034-2014 "Insulating Backplane for Crystalline Silicon Solar Cell Modules", set the temperature in the high temperature and high humidity box to 85°C, the humidity to 85%, the accumulation time to be 2000h, take out the sample for observation Appearance and test package strength. After testing the encapsulation strength, observe the appearance of the fluorocarbon coating, and those with no yellowing or bulging are qualified (ie OK) (see the appearance of the hot spot test in Table 1).
组件热斑测试根据IEC61215标准进行测试,选取182mm硅片的78片电池组件进行实验室测试。测试条件为85℃,85%湿度,分别测试96h和192h的功率衰减(功率变更数据)。功率衰减值越低,抗PID性能越好。The module hot spot test is tested according to the IEC61215 standard, and 78 cell modules with 182mm silicon wafers are selected for laboratory testing. The test conditions were 85° C., 85% humidity, and the power decay (power change data) was tested for 96h and 192h, respectively. The lower the power decay value, the better the anti-PID performance.
下面将结合实施例进一步说明本发明提供的氟碳涂布液和氟碳层。The fluorocarbon coating solution and the fluorocarbon layer provided by the present invention will be further described below with reference to the examples.
实施例1Example 1
本实施例提供的氟碳涂布液制备方法包括:The preparation method of the fluorocarbon coating solution provided in this embodiment includes:
将70%的聚四氟乙烯类型氟碳树脂,5%的纳米二氧化铈UV吸收剂,粒径在10~30nm,3%的消光粉,0.5%聚丙烯酸酯添加剂,12%的热塑性聚氨酯,9.5%的异氰酸酯。将主体树脂分散在有机溶剂中,形成固含量58%的氟碳涂布液。其中聚四氟乙烯类型氟碳树脂由大金氟化工提供,纳米二氧化铈吸收剂由毕克化学提供,消光粉由格雷斯有限公司提供,聚丙烯酸酯由毕克化学提供,热塑性聚氨酯由禾大化学提供的,异氰酸酯由拜耳公司提供,有机溶剂为乙酸丁酯。70% polytetrafluoroethylene type fluorocarbon resin, 5% nano ceria UV absorber, particle size is 10~30nm, 3% matting powder, 0.5% polyacrylate additive, 12% thermoplastic polyurethane, 9.5% isocyanate. The host resin was dispersed in an organic solvent to form a fluorocarbon coating liquid with a solid content of 58%. Among them, the PTFE type fluorocarbon resin is provided by Daikin Fluorochemical, the nano ceria absorber is provided by BYK, the matting powder is provided by Grace Co., Ltd., the polyacrylate is provided by BYK, and the thermoplastic polyurethane is provided by He The isocyanate was provided by DaChem, the isocyanate was provided by Bayer, and the organic solvent was butyl acetate.
将涂层涂在透明PET(厚度为275μm)上,涂层厚度为16μm。The coating was applied on transparent PET (275 μm thick) with a coating thickness of 16 μm.
制得的氟碳涂层的性能测试结果见表1。The performance test results of the prepared fluorocarbon coatings are shown in Table 1.
实施例2Example 2
本实施例提供的氟碳涂布液制备方法包括:The preparation method of the fluorocarbon coating solution provided in this embodiment includes:
将50%的聚四氟乙烯类型氟碳树脂,10%的纳米二氧化铈UV吸收剂,粒径在10~30nm,4%的消光粉,0.8%聚丙烯酸酯添加剂,15.2%的热塑性聚氨酯,20%的异氰酸酯。将主体树脂分散在有机溶剂中,形成固含量50%的氟碳涂布液。其中聚四氟乙烯类型氟碳树脂由大金氟化工提供,纳米二氧化铈吸收剂由毕克化学提供,消光粉由格雷斯有限公司提供,聚丙烯酸酯由毕克化学提供,热塑性聚氨酯由禾大化学提供的,异氰酸酯由拜耳公司提供,有机溶剂为乙酸丁酯。50% polytetrafluoroethylene type fluorocarbon resin, 10% nano ceria UV absorber, particle size is 10~30nm, 4% matting powder, 0.8% polyacrylate additive, 15.2% thermoplastic polyurethane, 20% isocyanate. The host resin was dispersed in an organic solvent to form a fluorocarbon coating liquid with a solid content of 50%. Among them, the PTFE type fluorocarbon resin is provided by Daikin Fluorochemical, the nano ceria absorber is provided by BYK, the matting powder is provided by Grace Co., Ltd., the polyacrylate is provided by BYK, and the thermoplastic polyurethane is provided by He The isocyanate was provided by DaChem, the isocyanate was provided by Bayer, and the organic solvent was butyl acetate.
将涂层涂在透明PET(厚度为300μm)上,涂层厚度为25μm。The coating was applied on transparent PET (300 μm thick) with a coating thickness of 25 μm.
制得的氟碳涂层的性能测试结果见表1。The performance test results of the prepared fluorocarbon coatings are shown in Table 1.
实施例3Example 3
本实施例提供的氟碳涂布液制备方法包括:The preparation method of the fluorocarbon coating solution provided in this embodiment includes:
将80%的聚四氟乙烯类型氟碳树脂,1.4%的纳米二氧化铈UV吸收剂,粒径在10~30nm,1%的消光粉,0.5%聚丙烯酸酯添加剂,10%的热塑性聚氨酯,7.1%的异氰酸酯。将主体树脂分散在有机溶剂中,形成固含量70%的氟碳涂布液。其中聚四氟乙烯类型氟碳树脂由大金氟化工提供,纳米二氧化铈吸收剂由毕克化学提供,消光粉由格雷斯有限公司提供,聚丙烯酸酯由毕克化学提供,热塑性聚氨酯由禾大化学提供的,异氰酸酯由拜耳公司提供,有机溶剂为乙酸丁酯。80% polytetrafluoroethylene type fluorocarbon resin, 1.4% nano ceria UV absorber, particle size 10-30nm, 1% matting powder, 0.5% polyacrylate additive, 10% thermoplastic polyurethane, 7.1% isocyanate. The host resin was dispersed in an organic solvent to form a fluorocarbon coating liquid with a solid content of 70%. Among them, the PTFE type fluorocarbon resin is provided by Daikin Fluorochemical, the nano ceria absorber is provided by BYK, the matting powder is provided by Grace Co., Ltd., the polyacrylate is provided by BYK, and the thermoplastic polyurethane is provided by He The isocyanate was provided by DaChem, the isocyanate was provided by Bayer, and the organic solvent was butyl acetate.
将涂层涂在透明PET(厚度为250μm)上,涂层厚度为10μm。The coating was applied on transparent PET (250 μm thick) with a coating thickness of 10 μm.
制得的氟碳涂层的性能测试结果见表1。The performance test results of the prepared fluorocarbon coatings are shown in Table 1.
实施例4Example 4
本实施例提供的氟碳涂布液制备方法包括:The preparation method of the fluorocarbon coating solution provided in this embodiment includes:
将65%的聚四氟乙烯类型氟碳树脂,6%的纳米二氧化铈UV吸收剂,粒径在10~30nm,2%的消光粉,0.4%聚丙烯酸酯添加剂,13%的热塑性聚氨酯,13.6%的异氰酸酯。将主体树脂分散在有机溶剂中,形成固含量62%的氟碳涂布液。其中聚四氟乙烯类型氟碳树脂由大金氟化工提供,纳米二氧化铈吸收剂由毕克化学提供,消光粉由格雷斯有限公司提供,聚丙烯酸酯由毕克化学提供,热塑性聚氨酯由禾大化学提供的,异氰酸酯由拜耳公司提供,有机溶剂为乙酸丁酯。65% polytetrafluoroethylene type fluorocarbon resin, 6% nano ceria UV absorber, particle size 10-30nm, 2% matting powder, 0.4% polyacrylate additive, 13% thermoplastic polyurethane, 13.6% isocyanate. The host resin was dispersed in an organic solvent to form a fluorocarbon coating liquid with a solid content of 62%. Among them, the PTFE type fluorocarbon resin is provided by Daikin Fluorochemical, the nano ceria absorber is provided by BYK, the matting powder is provided by Grace Co., Ltd., the polyacrylate is provided by BYK, and the thermoplastic polyurethane is provided by He The isocyanate was provided by DaChem, the isocyanate was provided by Bayer, and the organic solvent was butyl acetate.
将涂层涂在透明PET(厚度为275μm)上,涂层厚度为17μm。The coating was applied on transparent PET (275 μm thick) with a coating thickness of 17 μm.
制得的氟碳涂层的性能测试结果见表1。The performance test results of the prepared fluorocarbon coatings are shown in Table 1.
实施例5Example 5
本实施例提供的氟碳涂布液制备方法包括:The preparation method of the fluorocarbon coating solution provided in this embodiment includes:
将62%的聚四氟乙烯类型氟碳树脂,7%的纳米二氧化铈UV吸收剂,粒径在10~30nm,3%的消光粉,0.4%聚丙烯酸酯添加剂,14.6%的热塑性聚氨酯,13%的异氰酸酯。将主体树脂分散在有机溶剂中,形成固含量65%的氟碳涂布液。其中聚四氟乙烯类型氟碳树脂由大金氟化工提供,纳米二氧化铈吸收剂由毕克化学提供,消光粉由格雷斯有限公司提供,聚丙烯酸酯由毕克化学提供,热塑性聚氨酯由禾大化学提供的,异氰酸酯由拜耳公司提供,有机溶剂为乙酸丁酯。62% polytetrafluoroethylene type fluorocarbon resin, 7% nano ceria UV absorber, particle size 10-30nm, 3% matting powder, 0.4% polyacrylate additive, 14.6% thermoplastic polyurethane, 13% isocyanate. The host resin was dispersed in an organic solvent to form a fluorocarbon coating liquid with a solid content of 65%. Among them, the PTFE type fluorocarbon resin is provided by Daikin Fluorochemical, the nano ceria absorber is provided by BYK, the matting powder is provided by Grace Co., Ltd., the polyacrylate is provided by BYK, and the thermoplastic polyurethane is provided by He The isocyanate was provided by DaChem, the isocyanate was provided by Bayer, and the organic solvent was butyl acetate.
将涂层涂在透明PET(厚度为300μm)上,涂层厚度为15μm。The coating was applied on transparent PET (300 μm thick) with a coating thickness of 15 μm.
制得的氟碳涂层的性能测试结果见表1。The performance test results of the prepared fluorocarbon coatings are shown in Table 1.
实施例6Example 6
本实施例提供的氟碳涂布液制备方法包括:The preparation method of the fluorocarbon coating solution provided in this embodiment includes:
将55%的聚四氟乙烯类型氟碳树脂,3%的纳米二氧化铈UV吸收剂,粒径在10~30nm,4.5%的消光粉,0.3%聚丙烯酸酯添加剂,20%的热塑性聚氨酯,17.2%的异氰酸酯。将主体树脂分散在有机溶剂中,形成固含量54%的氟碳涂布液。其中聚四氟乙烯类型氟碳树脂由大金氟化工提供,纳米二氧化铈吸收剂由毕克化学提供,消光粉由格雷斯有限公司提供,聚丙烯酸酯由毕克化学提供,热塑性聚氨酯由禾大化学提供的,异氰酸酯由拜耳公司提供,有机溶剂为乙酸丁酯。55% polytetrafluoroethylene type fluorocarbon resin, 3% nano ceria UV absorber, particle size is 10~30nm, 4.5% matting powder, 0.3% polyacrylate additive, 20% thermoplastic polyurethane, 17.2% isocyanate. The host resin was dispersed in an organic solvent to form a fluorocarbon coating liquid with a solid content of 54%. Among them, the PTFE type fluorocarbon resin is provided by Daikin Fluorochemical, the nano ceria absorber is provided by BYK, the matting powder is provided by Grace Co., Ltd., the polyacrylate is provided by BYK, and the thermoplastic polyurethane is provided by He The isocyanate was provided by DaChem, the isocyanate was provided by Bayer, and the organic solvent was butyl acetate.
将涂层涂在透明PET(厚度为300μm)上,涂层厚度为22μm。The coating was applied on transparent PET (300 μm thick) with a coating thickness of 22 μm.
制得的氟碳涂层的性能测试结果见表1。The performance test results of the prepared fluorocarbon coatings are shown in Table 1.
实施例7Example 7
本实施例提供的氟碳涂布液制备方法包括:The preparation method of the fluorocarbon coating solution provided in this embodiment includes:
将58%的聚四氟乙烯类型氟碳树脂,9%的纳米二氧化铈UV吸收剂,粒径在10~30nm,4%的消光粉,0.3%聚丙烯酸酯添加剂,16.4%的热塑性聚氨酯,12.3%的异氰酸酯。将主体树脂分散在有机溶剂中,形成固含量68%的氟碳涂布液。其中聚四氟乙烯类型氟碳树脂由大金氟化工提供,纳米二氧化铈吸收剂由毕克化学提供,消光粉由格雷斯有限公司提供,聚丙烯酸酯由毕克化学提供,热塑性聚氨酯由禾大化学提供的,异氰酸酯由拜耳公司提供,有机溶剂为乙酸丁酯。58% polytetrafluoroethylene type fluorocarbon resin, 9% nano ceria UV absorber, particle size 10-30nm, 4% matting powder, 0.3% polyacrylate additive, 16.4% thermoplastic polyurethane, 12.3% isocyanate. The host resin was dispersed in an organic solvent to form a fluorocarbon coating liquid with a solid content of 68%. Among them, the PTFE type fluorocarbon resin is provided by Daikin Fluorochemical, the nano ceria absorber is provided by BYK, the matting powder is provided by Grace Co., Ltd., the polyacrylate is provided by BYK, and the thermoplastic polyurethane is provided by He The isocyanate was provided by DaChem, the isocyanate was provided by Bayer, and the organic solvent was butyl acetate.
将涂层涂在透明PET(厚度为300μm)上,涂层厚度为20μm。The coating was applied on transparent PET (300 μm thick) with a coating thickness of 20 μm.
制得的氟碳涂层的性能测试结果见表1。The performance test results of the prepared fluorocarbon coatings are shown in Table 1.
实施例8Example 8
本实施例提供的氟碳涂布液制备方法包括:The preparation method of the fluorocarbon coating solution provided in this embodiment includes:
将63.5%的聚四氟乙烯类型氟碳树脂,7.8%的纳米二氧化铈UV吸收剂,粒径在10~30nm,5%的消光粉,0.7%聚丙烯酸酯添加剂,18%的热塑性聚氨酯,5%的异氰酸酯。将主体树脂分散在有机溶剂中,形成固含量56%的氟碳涂布液。其中聚四氟乙烯类型氟碳树脂由大金氟化工提供,纳米二氧化铈吸收剂由毕克化学提供,消光粉由格雷斯有限公司提供,聚丙烯酸酯由毕克化学提供,热塑性聚氨酯由禾大化学提供的,异氰酸酯由拜耳公司提供,有机溶剂为乙酸丁酯。63.5% polytetrafluoroethylene type fluorocarbon resin, 7.8% nano ceria UV absorber,
将涂层涂在透明PET(厚度为275μm)上,涂层厚度为16μm。The coating was applied on transparent PET (275 μm thick) with a coating thickness of 16 μm.
制得的氟碳涂层的性能测试结果见表1。The performance test results of the prepared fluorocarbon coatings are shown in Table 1.
对比例1Comparative Example 1
本对比例提供的氟碳涂布液制备方法包括:The preparation method of the fluorocarbon coating solution provided in this comparative example includes:
将65%的聚四氟乙烯类型氟碳树脂,0%的纳米二氧化铈UV吸收剂,2%的消光粉,0.4%聚丙烯酸酯添加剂,19%的热塑性聚氨酯,13.6%的异氰酸酯。将主体树脂分散在有机溶剂中,形成固含量62%的氟碳涂布液。其中聚四氟乙烯类型氟碳树脂由大金氟化工提供,消光粉由格雷斯有限公司提供,聚丙烯酸酯由毕克化学提供,热塑性聚氨酯由禾大化学提供的,异氰酸酯由拜耳公司提供,有机溶剂为乙酸丁酯。65% PTFE type fluorocarbon resin, 0% nano ceria UV absorber, 2% matting powder, 0.4% polyacrylate additive, 19% thermoplastic polyurethane, 13.6% isocyanate. The host resin was dispersed in an organic solvent to form a fluorocarbon coating liquid with a solid content of 62%. Among them, PTFE type fluorocarbon resin is provided by Daikin Fluorochemical, matting powder is provided by Grace Co., Ltd., polyacrylate is provided by BYK, thermoplastic polyurethane is provided by Croda Chemical, isocyanate is provided by Bayer, organic The solvent was butyl acetate.
将涂层涂在透明PET(厚度为275μm)上,涂层厚度为16μm。The coating was applied on transparent PET (275 μm thick) with a coating thickness of 16 μm.
制得的氟碳涂层的性能测试结果见表1。The performance test results of the prepared fluorocarbon coatings are shown in Table 1.
对比例2Comparative Example 2
本对比例提供的氟碳涂布液制备方法包括:The preparation method of the fluorocarbon coating solution provided in this comparative example includes:
将50%的聚四氟乙烯类型氟碳树脂,20%的纳米二氧化铈UV吸收剂,粒径在10~30nm,2%的消光粉,0.4%聚丙烯酸酯添加剂,14%的热塑性聚氨酯,13.6%的异氰酸酯。将主体树脂分散在有机溶剂中,形成固含量62%的氟碳涂布液。其中聚四氟乙烯类型氟碳树脂由大金氟化工提供,纳米二氧化铈吸收剂由毕克化学提供,消光粉由格雷斯有限公司提供,聚丙烯酸酯由毕克化学提供,热塑性聚氨酯由禾大化学提供的,异氰酸酯由拜耳公司提供,有机溶剂为乙酸丁酯。50% polytetrafluoroethylene type fluorocarbon resin, 20% nano ceria UV absorber, particle size is 10~30nm, 2% matting powder, 0.4% polyacrylate additive, 14% thermoplastic polyurethane, 13.6% isocyanate. The host resin was dispersed in an organic solvent to form a fluorocarbon coating liquid with a solid content of 62%. Among them, the PTFE type fluorocarbon resin is provided by Daikin Fluorochemical, the nano ceria absorber is provided by BYK, the matting powder is provided by Grace Co., Ltd., the polyacrylate is provided by BYK, and the thermoplastic polyurethane is provided by He The isocyanate was provided by DaChem, the isocyanate was provided by Bayer, and the organic solvent was butyl acetate.
将涂层涂在透明PET(厚度为275μm)上,涂层厚度为16μm。The coating was applied on transparent PET (275 μm thick) with a coating thickness of 16 μm.
制得的氟碳涂层的性能测试结果见表1。The performance test results of the prepared fluorocarbon coatings are shown in Table 1.
对比例3Comparative Example 3
本对比例提供的氟碳涂布液制备方法包括:The preparation method of the fluorocarbon coating solution provided in this comparative example includes:
将65%的聚四氟乙烯类型氟碳树脂,6%的纳米二氧化铈UV吸收剂,粒径在50~80nm,2%的消光粉,0.4%聚丙烯酸酯添加剂,13%的热塑性聚氨酯,13.6%的异氰酸酯。将主体树脂分散在有机溶剂中,形成固含62%的氟碳涂布液。其中聚四氟乙烯类型氟碳树脂由大金氟化工提供,纳米二氧化铈吸收剂由毕克化学提供,消光粉由格雷斯有限公司提供,聚丙烯酸酯由毕克化学提供,热塑性聚氨酯由禾大化学提供的,异氰酸酯由拜耳公司提供,有机溶剂为乙酸丁酯。65% polytetrafluoroethylene type fluorocarbon resin, 6% nano ceria UV absorber, particle size 50~80nm, 2% matting powder, 0.4% polyacrylate additive, 13% thermoplastic polyurethane, 13.6% isocyanate. The host resin was dispersed in an organic solvent to form a fluorocarbon coating solution with a solid content of 62%. Among them, the PTFE type fluorocarbon resin is provided by Daikin Fluorochemical, the nano ceria absorber is provided by BYK, the matting powder is provided by Grace Co., Ltd., the polyacrylate is provided by BYK, and the thermoplastic polyurethane is provided by He The isocyanate was provided by DaChem, the isocyanate was provided by Bayer, and the organic solvent was butyl acetate.
将涂层涂在透明PET上(厚度为275μm),涂层厚度为16μm。The coating was applied on transparent PET (275 μm thick) with a coating thickness of 16 μm.
制得的氟碳涂层的性能测试结果见表1。The performance test results of the prepared fluorocarbon coatings are shown in Table 1.
对比例4Comparative Example 4
本对比例提供的氟碳涂布液制备方法包括:The preparation method of the fluorocarbon coating solution provided in this comparative example includes:
将65%的聚四氟乙烯类型氟碳树脂,6%的纳米二氧化铈UV吸收剂,粒径在200nm,2%的消光粉,0.4%聚丙烯酸酯添加剂,13%的热塑性聚氨酯,13.6%的异氰酸酯。将主体树脂分散在有机溶剂中,形成固含量62%的氟碳涂布液。其中聚四氟乙烯类型氟碳树脂由大金氟化工提供,纳米二氧化铈吸收剂由毕克化学提供,消光粉由格雷斯有限公司提供,聚丙烯酸酯由毕克化学提供,热塑性聚氨酯由禾大化学提供的,异氰酸酯由拜耳公司提供,有机溶剂为乙酸丁酯。65% PTFE type fluorocarbon resin, 6% nano ceria UV absorber, particle size 200nm, 2% matting powder, 0.4% polyacrylate additive, 13% thermoplastic polyurethane, 13.6% of isocyanates. The host resin was dispersed in an organic solvent to form a fluorocarbon coating liquid with a solid content of 62%. Among them, the PTFE type fluorocarbon resin is provided by Daikin Fluorochemical, the nano ceria absorber is provided by BYK, the matting powder is provided by Grace Co., Ltd., the polyacrylate is provided by BYK, and the thermoplastic polyurethane is provided by He The isocyanate was provided by DaChem, the isocyanate was provided by Bayer, and the organic solvent was butyl acetate.
将涂层涂在透明PET(厚度为275μm)上,涂层厚度为16μm。The coating was applied on transparent PET (275 μm thick) with a coating thickness of 16 μm.
制得的氟碳涂层的性能测试结果见表1。The performance test results of the prepared fluorocarbon coatings are shown in Table 1.
对比例5Comparative Example 5
本对比例提供的氟碳涂布液制备方法包括:The preparation method of the fluorocarbon coating solution provided in this comparative example includes:
将65%的聚四氟乙烯类型氟碳树脂,6%的苯并三唑类UV吸收剂,2%的消光粉,0.4%聚丙烯酸酯添加剂,13%的热塑性聚氨酯,13.6%的异氰酸酯。将主体树脂分散在有机溶剂中,形成固含量62%的氟碳涂布液。其中聚四氟乙烯类型氟碳树脂由大金氟化工提供,纳米二氧化铈吸收剂由毕克化学提供,消光粉由格雷斯有限公司提供,聚丙烯酸酯由毕克化学提供,热塑性聚氨酯由禾大化学提供的,异氰酸酯由拜耳公司提供,有机溶剂为乙酸丁酯。65% polytetrafluoroethylene type fluorocarbon resin, 6% benzotriazole type UV absorber, 2% matting powder, 0.4% polyacrylate additive, 13% thermoplastic polyurethane, 13.6% isocyanate. The host resin was dispersed in an organic solvent to form a fluorocarbon coating liquid with a solid content of 62%. Among them, the PTFE type fluorocarbon resin is provided by Daikin Fluorochemical, the nano ceria absorber is provided by BYK, the matting powder is provided by Grace Co., Ltd., the polyacrylate is provided by BYK, and the thermoplastic polyurethane is provided by He The isocyanate was provided by DaChem, the isocyanate was provided by Bayer, and the organic solvent was butyl acetate.
将涂层涂在透明PET(厚度为275μm)上,涂层厚度为16μm。The coating was applied on transparent PET (275 μm thick) with a coating thickness of 16 μm.
制得的氟碳涂层的性能测试结果见表1。The performance test results of the prepared fluorocarbon coatings are shown in Table 1.
将实施例1至8和对比例1至5中的氟膜(氟碳涂层+基材)进行下述测试:按照GB1720-1979《漆膜附着力测定法》的标准,测试氟碳层的附着力,其中100/100代表不脱膜,90/100代表脱落10%。按照JISK7105-1981《塑料光学性能的测试方法》的标准,测试各氟膜(氟碳涂层+基材)的全光线透过率。按照GB/T 31034-2014《晶体硅太阳能电池组件用绝缘背板》的标准,测试太阳能背板的封装强度、耐湿热老化特性以及QUV变化。按照IEC61215标准进行测试组件热斑性能。The fluorine films (fluorocarbon coating+substrate) in Examples 1 to 8 and Comparative Examples 1 to 5 were tested as follows: According to the standard of GB1720-1979 "Determination of Paint Film Adhesion", the fluorocarbon layer was tested. Adhesion, where 100/100 means no release, 90/100 means 10% shedding. According to the standard of JISK7105-1981 "Test method for optical properties of plastics", the total light transmittance of each fluorine film (fluorocarbon coating + substrate) was tested. According to the standard of GB/T 31034-2014 "Insulation Backsheet for Crystalline Silicon Solar Cell Modules", the packaging strength, humidity and heat aging resistance and QUV change of the solar backsheet are tested. The component hot spot performance is tested according to the IEC61215 standard.
表1实施例1至8和对比例1至5中的氟膜(氟碳涂层+基材)测试结果Table 1 Test results of fluorine films (fluorocarbon coating + substrate) in Examples 1 to 8 and Comparative Examples 1 to 5
从表1中可以看到,当使用有机苯并三唑类的UV吸收剂时,UV测试性能较差,用背板做成的光伏组件在测试热斑性能时也容易造成外观黄变。这是因为苯并三唑类型的吸收剂耐高温性能较差,容易发生分子高温分解。而利用50~80nm的氧化铈会直接造成透明背板的透过率下降。利用更大粒子的氧化铈,在湿热测试、UV测试都有不利影响。上述结果表明,在高温耐热性效果上,合适粒径的纳米氧化铈会比有机小分子UV吸收剂更具备优势,可以在大功率组件热斑测试过程中体现出优势。As can be seen from Table 1, when an organic benzotriazole UV absorber is used, the UV test performance is poor, and the photovoltaic module made of the back sheet is also prone to yellowing in appearance when testing the hot spot performance. This is because benzotriazole-type absorbents have poor high temperature resistance and are prone to molecular pyrolysis. The use of 50-80 nm cerium oxide will directly cause the transmittance of the transparent backplane to decrease. The use of larger particles of cerium oxide has adverse effects on both the damp heat test and the UV test. The above results show that nano-cerium oxide with suitable particle size has more advantages than organic small molecule UV absorbers in the effect of high temperature heat resistance, and can show advantages in the process of hot spot test of high-power components.
本发明提供的氟膜(氟碳涂层+基材),同时可以保证封装强度、耐湿热效应、耐UV特性和热斑效应。其中,实施例1、4、5提供的氟膜(氟碳涂层+基材)性能最好,氟碳层不脱落,透光率超过90%,初始封装强度至少有90N/cm,在QUV测试120kwh/㎡后均无明显外观变化,经历高湿热老化测试封装强度至少有60N/cm,并且在热斑测试后外观均合格。The fluorine film (fluorocarbon coating + base material) provided by the present invention can simultaneously ensure the encapsulation strength, damp-heat resistance, UV resistance and hot spot effect. Among them, the fluorocarbon film (fluorocarbon coating + substrate) provided in Examples 1, 4 and 5 has the best performance, the fluorocarbon layer does not fall off, the light transmittance exceeds 90%, and the initial encapsulation strength is at least 90N/cm. After the test of 120kwh/㎡, there is no obvious change in appearance. After the high humidity and heat aging test, the package strength is at least 60N/cm, and the appearance is qualified after the hot spot test.
以上所述,仅为本发明的较佳实施例而已,并非用于限定本发明的保护范围。凡是根据本发明内容所做的均等变化与修饰,均涵盖在本发明的专利范围内。The above descriptions are merely preferred embodiments of the present invention, and are not intended to limit the protection scope of the present invention. All equivalent changes and modifications made according to the content of the present invention are covered within the patent scope of the present invention.
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Publication number | Priority date | Publication date | Assignee | Title |
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CN105419602A (en) * | 2015-12-18 | 2016-03-23 | 中国铁道科学研究院铁道建筑研究所 | Normal-temperature curable fluorocarbon coating for corrosion prevention and preparation method of fluorocarbon coating |
CN106784097A (en) * | 2017-02-22 | 2017-05-31 | 苏州赛伍应用技术有限公司 | A kind of transparent solar components backboard of high water resistant and foreboard |
CN110885593A (en) * | 2019-12-03 | 2020-03-17 | 苏州赛伍应用技术股份有限公司 | Transparent coating for photovoltaic back plate and photovoltaic back plate |
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CN105419602A (en) * | 2015-12-18 | 2016-03-23 | 中国铁道科学研究院铁道建筑研究所 | Normal-temperature curable fluorocarbon coating for corrosion prevention and preparation method of fluorocarbon coating |
CN106784097A (en) * | 2017-02-22 | 2017-05-31 | 苏州赛伍应用技术有限公司 | A kind of transparent solar components backboard of high water resistant and foreboard |
CN110885593A (en) * | 2019-12-03 | 2020-03-17 | 苏州赛伍应用技术股份有限公司 | Transparent coating for photovoltaic back plate and photovoltaic back plate |
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