CN101260196B - White polyester solar energy battery back film and preparation method thereof - Google Patents
White polyester solar energy battery back film and preparation method thereof Download PDFInfo
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- 229920000728 polyester Polymers 0.000 title claims abstract description 80
- 238000002360 preparation method Methods 0.000 title claims abstract description 9
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims abstract description 40
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 claims abstract description 40
- 239000004594 Masterbatch (MB) Substances 0.000 claims abstract description 34
- 239000000377 silicon dioxide Substances 0.000 claims abstract description 20
- 239000004408 titanium dioxide Substances 0.000 claims abstract description 20
- 235000012239 silicon dioxide Nutrition 0.000 claims abstract description 19
- 238000004381 surface treatment Methods 0.000 claims abstract description 9
- 239000002245 particle Substances 0.000 claims abstract description 8
- 238000002156 mixing Methods 0.000 claims description 6
- 238000010438 heat treatment Methods 0.000 claims description 3
- 239000012965 benzophenone Substances 0.000 claims description 2
- 239000006096 absorbing agent Substances 0.000 claims 4
- 229960001866 silicon dioxide Drugs 0.000 claims 4
- 238000002425 crystallisation Methods 0.000 claims 2
- 230000008025 crystallization Effects 0.000 claims 2
- RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 claims 1
- QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical compound C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 claims 1
- 239000012964 benzotriazole Substances 0.000 claims 1
- 230000004927 fusion Effects 0.000 claims 1
- 238000000227 grinding Methods 0.000 claims 1
- 238000005096 rolling process Methods 0.000 claims 1
- 229920006267 polyester film Polymers 0.000 abstract description 14
- 230000032683 aging Effects 0.000 abstract description 5
- 230000004888 barrier function Effects 0.000 abstract description 5
- 230000002745 absorbent Effects 0.000 abstract 1
- 239000002250 absorbent Substances 0.000 abstract 1
- 239000000203 mixture Substances 0.000 description 7
- 229940124543 ultraviolet light absorber Drugs 0.000 description 7
- 239000006097 ultraviolet radiation absorber Substances 0.000 description 7
- 238000004519 manufacturing process Methods 0.000 description 6
- 229920005989 resin Polymers 0.000 description 6
- 239000011347 resin Substances 0.000 description 6
- 239000000853 adhesive Substances 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- 239000006229 carbon black Substances 0.000 description 2
- 239000003431 cross linking reagent Substances 0.000 description 2
- 239000011363 dried mixture Substances 0.000 description 2
- 239000007888 film coating Substances 0.000 description 2
- 238000009501 film coating Methods 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 230000001681 protective effect Effects 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 239000002345 surface coating layer Substances 0.000 description 2
- 239000012855 volatile organic compound Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- IYAZLDLPUNDVAG-UHFFFAOYSA-N 2-(benzotriazol-2-yl)-4-(2,4,4-trimethylpentan-2-yl)phenol Chemical compound CC(C)(C)CC(C)(C)C1=CC=C(O)C(N2N=C3C=CC=CC3=N2)=C1 IYAZLDLPUNDVAG-UHFFFAOYSA-N 0.000 description 1
- IMSODMZESSGVBE-UHFFFAOYSA-N 2-Oxazoline Chemical compound C1CN=CO1 IMSODMZESSGVBE-UHFFFAOYSA-N 0.000 description 1
- 239000004925 Acrylic resin Substances 0.000 description 1
- 229920000178 Acrylic resin Polymers 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- 229920001807 Urea-formaldehyde Polymers 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 238000005054 agglomeration Methods 0.000 description 1
- 230000002776 aggregation Effects 0.000 description 1
- 150000008366 benzophenones Chemical class 0.000 description 1
- 150000001565 benzotriazoles Chemical class 0.000 description 1
- 239000003990 capacitor Substances 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000005034 decoration Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000018109 developmental process Effects 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 239000010410 layer Substances 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- 239000005022 packaging material Substances 0.000 description 1
- 238000004806 packaging method and process Methods 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000002985 plastic film Substances 0.000 description 1
- 229920006255 plastic film Polymers 0.000 description 1
- 229920001225 polyester resin Polymers 0.000 description 1
- 239000004645 polyester resin Substances 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
Classifications
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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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- Compositions Of Macromolecular Compounds (AREA)
- Photovoltaic Devices (AREA)
- Processes Of Treating Macromolecular Substances (AREA)
Abstract
Description
技术领域technical field
本发明涉及一种白色聚酯太阳能电池背膜及其制备方法,属于聚酯薄膜领域。The invention relates to a white polyester solar battery back film and a preparation method thereof, belonging to the field of polyester films.
背景技术Background technique
聚酯薄膜通常为无色透明,有光泽,强韧性和弹性均好的薄膜,与其他塑料薄膜相比,具有相对密度大、拉伸强度高,延伸率适中,冲击强度大,透气性小,耐热性好和透明度高、且无毒无害等优点,而广泛用于包装材料。随着科技的飞速发展,聚酯薄膜在电容器、感光材料、音像以及太阳电池方面等得到应用。如CN101065849A所公开的“易粘合性聚酯薄膜及使用其的太阳能电池背面保护膜”,由聚酯薄膜和涂布在该聚酯薄膜一面的树脂被膜构成,在聚酯薄膜的结晶取向结束之前,将树脂被膜涂液涂布在聚酯薄膜上,再进行干燥、拉伸、热处理定形而成易粘合性聚酯薄膜。这种太阳能电池保持膜由于是两层结构,制作工艺复杂,且需特殊的设备热加工,不仅制造成本高,而且加工表面涂布层时,表面涂布层的易被刮脱受损导致性能下降。另外由于树脂被膜是由树脂和交联剂构成,该树脂由聚酯树脂、丙烯树脂以及聚乙烯醇等组合而成,而交联剂含有噁唑啉基的聚合物或三聚氰胺、尿素树脂或环氧树脂,由于被膜涂液在制备过程中必须使用溶剂,而常规的溶剂含有可挥发的有机化合物,因此在制作聚酯薄膜和使用过程中,可挥发的有机化合物对环境造成一定的危害。而CN1286911C所公开的“一种黑色不透光型聚酯薄膜及其制备方法”,由聚酯切片、炭黑型黑色聚酯母料以及炭黑有机染料复合型黑色聚酯母料构成,该不透光型聚酯薄膜可达到黑色度均匀,表观光亮,热稳定性好等特点,但不耐老化,阻隔性能较差,只能用于装饰装潢、包装等,而不能用于太阳能电池的保护膜。Polyester film is usually colorless, transparent, glossy, with good strength, toughness and elasticity. Compared with other plastic films, it has high relative density, high tensile strength, moderate elongation, high impact strength and low air permeability. Good heat resistance and high transparency, and non-toxic and harmless, and widely used in packaging materials. With the rapid development of science and technology, polyester film has been applied in capacitors, photosensitive materials, audio and video, and solar cells. As disclosed in CN101065849A, "Easy Adhesive Polyester Film and Solar Cell Back Protective Film Using It" consists of a polyester film and a resin film coated on one side of the polyester film, and the crystallographic orientation of the polyester film ends Previously, the resin film coating solution was coated on the polyester film, and then dried, stretched, and heat-treated to form an easy-adhesive polyester film. Due to the two-layer structure of this solar cell holding film, the manufacturing process is complicated, and special equipment is required for thermal processing. Not only the manufacturing cost is high, but also when the surface coating layer is processed, the surface coating layer is easily scraped off and the performance is damaged. decline. In addition, because the resin film is composed of resin and cross-linking agent, the resin is composed of polyester resin, acrylic resin and polyvinyl alcohol, etc., and the cross-linking agent contains oxazoline-based polymers or melamine, urea resin or ring Oxygen resin, because solvents must be used in the preparation process of film coating liquid, and conventional solvents contain volatile organic compounds, so during the production and use of polyester films, volatile organic compounds cause certain harm to the environment. And CN1286911C discloses "a kind of black opaque polyester film and its preparation method", which is composed of polyester chip, carbon black type black polyester masterbatch and carbon black organic dye compound type black polyester masterbatch. Opaque polyester film can achieve uniform blackness, bright surface, good thermal stability, etc., but it is not resistant to aging and has poor barrier performance. It can only be used for decoration, packaging, etc., but not for solar cells. protective film.
发明内容Contents of the invention
本发明的目的是提供一种遮光性好,较好的抗老化性和阻隔性的白色聚酯太阳能电池背膜及其制备方法。The purpose of the present invention is to provide a white polyester solar cell back film with good light-shielding property, good aging resistance and barrier property and its preparation method.
本发明为达到上述目的的技术方案是:一种白色聚酯太阳能电池背膜,其特征在于:由聚酯切片和白色聚酯母料组成,按重量份数比,聚酯切片与白色聚酯母料比为1.0-9.0∶1,所述的白色聚酯母料含有以下组分,按重量百分比,35%-89.4%的聚酯切片、0.5%-10%的二氧化硅、10%-50%的二氧化钛和0.1-5%的紫外光吸收剂,二氧化硅经过有机化表面处理、且粒径在10-100nm,二氧化钛经有机化表面处理、粒径在100-1000nm。The technical scheme of the present invention to achieve the above object is: a white polyester solar cell back film, characterized in that: it is composed of polyester chips and white polyester masterbatch, and the ratio of polyester chips and white polyester The masterbatch ratio is 1.0-9.0:1, and the white polyester masterbatch contains the following components, by weight percentage, 35%-89.4% of polyester chips, 0.5%-10% of silicon dioxide, 10%- 50% of titanium dioxide and 0.1-5% of ultraviolet light absorber, the silicon dioxide undergoes organic surface treatment with a particle size of 10-100nm, and the titanium dioxide undergoes organic surface treatment with a particle size of 100-1000nm.
本发明白色聚酯太阳能电池背膜的制备方法,其特征在于:The preparation method of the white polyester solar cell back film of the present invention is characterized in that:
(1)、按重量百分比,将0.5%-10%的二氧化硅与10%-20%的聚酯切片在双螺杆挤出机中熔融状态下进行表面处理并挤出制成母粒、研磨待用,同样将10%-50%的二氧化钛与25%-69.4%聚酯切片在双螺杆挤出机中熔融状态下进行表面处理并挤出制成母粒、研磨待用,将前述两种母粒与0.1-5%的紫外光吸收剂在高速混料机中充分混合后,用双螺杆挤出机挤出制得白色聚酯母料;(1) According to weight percentage, 0.5%-10% of silicon dioxide and 10%-20% of polyester chips are surface-treated in a twin-screw extruder in a molten state and extruded to make masterbatches, ground Stand-by, similarly 10%-50% titanium dioxide and 25%-69.4% polyester chips are surface-treated in a twin-screw extruder in a molten state and extruded to make masterbatches, ground for use, and the aforementioned two The masterbatch and 0.1-5% of ultraviolet light absorber are fully mixed in a high-speed mixer, and then extruded with a twin-screw extruder to obtain a white polyester masterbatch;
(2)、将聚酯切片与白色聚酯母料按1.0-9.0∶1放入高速混料机内充分混合后,在真空转鼓中60-100℃温度下预结晶3-6小时;(2) Put polyester chips and white polyester masterbatch in a ratio of 1.0-9.0:1 into a high-speed mixer and fully mix, then pre-crystallize in a vacuum drum at a temperature of 60-100°C for 3-6 hours;
(3)、将预结晶后的混料在120-170℃温度下干燥2-6h;(3) Dry the pre-crystallized mixture at a temperature of 120-170° C. for 2-6 hours;
(4)、将干燥后的混料送入挤出机内在270-300℃温度下熔融、挤出、铸片,制成厚片;(4) Feed the dried mixture into an extruder to melt, extrude, and cast into sheets at a temperature of 270-300°C to make thick sheets;
(5)、厚片在50-85℃温度下预热,进入110℃-50℃的远红外加热区,用3m/min-5m/min的线速度纵向拉伸,纵向拉伸倍率在1.5-3.5;(5) The thick sheet is preheated at a temperature of 50-85°C, enters the far-infrared heating zone of 110°C-50°C, and stretches longitudinally at a line speed of 3m/min-5m/min, and the longitudinal stretching ratio is 1.5- 3.5;
(6)、将经过纵向拉伸的膜片在90-135℃温度下预热后,再在100-150℃温度下横向拉伸,横向拉伸的拉伸倍率在1.5-3.8;(6) After preheating the longitudinally stretched film at a temperature of 90-135° C., and then stretching it transversely at a temperature of 100-150° C., the stretching ratio of the transverse stretching is 1.5-3.8;
(7)、将膜片在200-240℃温度条件下定型后收卷。(7) After setting the film at a temperature of 200-240°C, it is wound up.
本发明的白色聚酯太阳能电池背膜由聚酯切片和白色聚酯母料组成,且白色聚酯母料采用二氧化硅、二氧化钛和紫外光吸收剂,由于加入了纳米级的二氧化硅,不仅使太阳能电池背膜的结晶度明显提高,而且因二氧化硅其经过有机化的表面处理,在二氧化硅的表面引入羧基,使二氧化硅与聚酯基体间以化学键结合,从而提高了两者的结合力,使该太阳能电池背膜具有良好的阻隔性和低吸水性,有效地防止了水、氧、腐蚀性气液体等对太阳能电池的侵蚀。本发明加入了经过表面处理的二氧化钛,改善二氧化钛被光线活化的性质,使二氧化钛在太阳能电池背膜中具有较好的分散性和遮光性,而且白色的二氧化钛与紫外光吸收剂混合后,使该太阳能电池背膜在保持原有聚酯薄膜的优良物理性能的同时,具有更好的遮光性和耐老化性,提高了太阳能电池的使用寿命。本发明采用先制备白色聚酯母料,再与聚酯切片共混制成背膜,能保证物料的充分混合,尤其二氧化钛和二氧化硅表面均经过有机化处理,故在太阳能电池背膜中具有较好的分散性,加之对聚酯切片和白色聚酯母料的混料先进行低温预结晶,再进行干燥处理,杜绝了直接高温干燥引起的混料结块的问题,使太阳能电池背膜的白色更加均匀、性能稳定。本发明由于工业化生产稳定,生产工艺性好,可采用现有加工设备即可制得本发明的白色聚酯太阳能电池背膜,能降低制造成本。The white polyester solar cell back film of the present invention is made up of polyester chip and white polyester masterbatch, and white polyester masterbatch adopts silicon dioxide, titanium dioxide and ultraviolet light absorber, owing to adding nano-scale silicon dioxide, Not only the crystallinity of the solar cell back film is significantly improved, but also because of the organic surface treatment of the silicon dioxide, carboxyl groups are introduced on the surface of the silicon dioxide, so that the silicon dioxide and the polyester matrix are chemically bonded, thereby improving the The combination of the two makes the solar cell back film have good barrier properties and low water absorption, effectively preventing the solar cell from being corroded by water, oxygen, corrosive gas and liquid, etc. The present invention adds surface-treated titanium dioxide to improve the properties of titanium dioxide activated by light, so that titanium dioxide has better dispersibility and light-shielding properties in the back film of solar cells, and after white titanium dioxide is mixed with an ultraviolet light absorber, the While maintaining the excellent physical properties of the original polyester film, the solar cell back film has better light-shielding properties and aging resistance, which improves the service life of the solar cell. In the present invention, the white polyester masterbatch is prepared first, and then blended with polyester slices to form a back film, which can ensure sufficient mixing of materials, especially the surfaces of titanium dioxide and silicon dioxide have been organically treated, so they are used in the back film of solar cells It has good dispersibility. In addition, the mixture of polyester chips and white polyester masterbatch is pre-crystallized at low temperature first, and then dried, which eliminates the problem of agglomeration of the mixture caused by direct high-temperature drying. The white color of the film is more uniform and the performance is stable. The present invention has stable industrialized production and good production processability, and the white polyester solar cell back film of the present invention can be prepared by using existing processing equipment, which can reduce the manufacturing cost.
具体实施方式Detailed ways
本发明的白色聚酯太阳能电池背膜,由聚酯切片和白色聚酯母料组分,按重量份数比,聚酯切片与白色聚酯母料比为1.0-9.0∶1,该聚酯切片采用瓶级或膜级,具体重量份数比如表1所示,The white polyester solar battery back film of the present invention is composed of polyester chips and white polyester masterbatch components. Slicing adopts bottle grade or film grade, and the specific weight parts are as shown in Table 1,
表1Table 1
按重量百分比,本发明的白色聚酯母料具有以下组分:35%-89.4%的聚酯切片、0.5%-10%的二氧化硅、10%-50%的二氧化钛和0.1-5%的紫外光吸收剂,二氧化硅是经过有机化表面处理、且粒径在10-100nm,二氧化钛是经过有机化表面处理、且粒径在100-1000nm。该白色聚酯母料最好是50%-75%的聚酯切片、1%-7%的二氧化硅、23%-40%的二氧化钛和1-3%的紫外光吸收剂。用于白色聚酯母料的聚酯切片选用高粘度聚酯切片,紫外光吸收剂选用苯并三唑类或二苯甲酮类,具体重量百分比见表2所示,Percentage by weight, the white polyester masterbatch of the present invention has the following components: 35%-89.4% polyester chips, 0.5%-10% silicon dioxide, 10%-50% titanium dioxide and 0.1-5% As for the ultraviolet light absorber, silicon dioxide is treated with an organic surface and has a particle size of 10-100nm, and titanium dioxide is treated with an organic surface and has a particle size of 100-1000nm. The white polyester masterbatch is preferably 50%-75% polyester chip, 1%-7% silicon dioxide, 23%-40% titanium dioxide and 1-3% ultraviolet absorber. The polyester chips used for the white polyester masterbatch are selected from high-viscosity polyester chips, and the ultraviolet light absorbers are selected from benzotriazoles or benzophenones, and the specific weight percentages are shown in Table 2.
表2Table 2
本发明的白色聚酯太阳能电池背膜的制备方法如下:The preparation method of white polyester solar cell back film of the present invention is as follows:
(1)、按重量百分比,将0.5%-10%的二氧化硅与10%-20%的聚酯切片在双螺杆挤出机中熔融状态下进行表面处理并挤出制成母粒、研磨待用,同样将10%-50%的二氧化钛与25%-69.4%的聚酯切片在双螺杆挤出机中熔融状态下进行表面处理并挤出制成母粒、研磨待用,将前述两种母粒与0.1-5%的紫外光吸收剂在混料机中充分混合后,混料机的转速≥300r/min,用双螺杆挤出机挤出制得白色聚酯母料。该白色聚酯母料具体重量百分比可如表2所示。(1) According to weight percentage, 0.5%-10% of silicon dioxide and 10%-20% of polyester chips are surface-treated in a twin-screw extruder in a molten state and extruded to make masterbatches, ground Stand-by, similarly surface treat 10%-50% titanium dioxide and 25%-69.4% polyester chips in a twin-screw extruder in a molten state and extrude them into masterbatches, grind them for use, and mix the above two After fully mixing the seed masterbatch and 0.1-5% ultraviolet light absorber in a mixer, the speed of the mixer is more than 300r/min, extruding with a twin-screw extruder to obtain a white polyester masterbatch. The specific weight percentage of the white polyester masterbatch can be shown in Table 2.
(2)、将聚酯切片与白色聚酯母料按1.0-9.0∶1的重量份数放入混料机内充分混合,混料机的转速≥300r/min,聚酯切片与白色聚酯母料具体重量份数比可如表1所示,再在真空转鼓中以60-100℃的温度下预结晶3-6小时。(2) Put the polyester chips and white polyester masterbatch into the blender in a weight ratio of 1.0-9.0:1 and fully mix them. The speed of the blender is ≥300r/min. Polyester chips and white polyester The specific weight and part ratio of the masterbatch can be shown in Table 1, and then pre-crystallized in a vacuum drum at a temperature of 60-100° C. for 3-6 hours.
(3)、将预结晶后的混料在120-170℃温度下干燥2-6h,将水分控制在低于30ppm。(3) Dry the pre-crystallized mixture at a temperature of 120-170° C. for 2-6 hours, and control the moisture content below 30 ppm.
(4)、将干燥后的混料送入挤出机内在270-300℃温度下熔融、挤出、铸片,制成厚片;(4) Feed the dried mixture into an extruder to melt, extrude, and cast into sheets at a temperature of 270-300°C to make thick sheets;
(5)、厚片先经50-85℃温度下预热,再进入110℃-50℃的远红外加热区,用3m/min-5m/min的线速度纵向拉伸,纵向拉伸倍率控制在1.5-3.5。(5) The thick sheet is first preheated at 50-85°C, and then enters the far-infrared heating zone of 110°C-50°C, stretched longitudinally at a line speed of 3m/min-5m/min, and the longitudinal stretching ratio is controlled In 1.5-3.5.
(6)、将经过纵向拉伸的膜片在90-135℃温度下进行预热,再在100-150℃温度下横向拉伸,横向拉伸的拉伸倍率控制在1.5-3.8。(6) Preheating the longitudinally stretched film at a temperature of 90-135° C., and then stretching it transversely at a temperature of 100-150° C., the stretching ratio of the transverse stretching is controlled at 1.5-3.8.
(7)、膜片在200-240℃温度条件下定型,最后收卷制得白色聚酯太阳能电池背膜。(7) The diaphragm is shaped at a temperature of 200-240° C., and finally wound to obtain a white polyester solar battery back film.
分别对本发明的各实施例进行测试,测试结果见表3。Each embodiment of the present invention was tested respectively, and the test results are shown in Table 3.
表3table 3
从表3可以看出,本发明的白色聚酯太阳能电池背膜具有良好的遮光性、绝缘性能以及较好的抗老化性和阻隔性。It can be seen from Table 3 that the white polyester solar cell back film of the present invention has good light-shielding properties, insulating properties, and good aging resistance and barrier properties.
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KR101268217B1 (en) * | 2010-03-31 | 2013-06-10 | 코오롱인더스트리 주식회사 | Thermo-shrinkable polyester mono-layer film |
CN101967272B (en) * | 2010-05-19 | 2012-05-30 | 四川东材科技集团股份有限公司 | Method for preparing polyester film for solar cell backsheet film |
CN102110728B (en) * | 2010-08-11 | 2012-11-14 | 宁波长阳科技有限公司 | Backing film of solar battery and preparation method thereof |
CN102492269B (en) * | 2011-12-06 | 2014-02-26 | 宁波长阳科技有限公司 | Weather-resistant white master batch, weather-resistant polyester material and preparation methods of weather-resistant white master batch and weather-resistant polyester material |
CN103435983A (en) * | 2013-08-06 | 2013-12-11 | 苏州金海薄膜科技发展有限公司 | Transparent colored heat and ultraviolet insulation film and preparation method thereof |
JP6352209B2 (en) * | 2015-03-25 | 2018-07-04 | 富士フイルム株式会社 | POLYESTER FILM AND PROCESS FOR PRODUCING THE SAME, SOLAR CELL BACK PROTECTION SHEET |
CN105038156A (en) * | 2015-08-28 | 2015-11-11 | 佛山杜邦鸿基薄膜有限公司 | Solar cell backboard polyester film with high reflectivity and preparing method of solar cell backboard polyester film |
CN106905671A (en) * | 2016-12-23 | 2017-06-30 | 宁波长阳科技股份有限公司 | A kind of PET water vapour locking is every master batch and preparation method thereof |
CN116814048A (en) * | 2023-06-29 | 2023-09-29 | 常州勤邦新材料科技有限公司 | A functional masterbatch for producing UV-resistant polyester chips |
Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1176004A1 (en) * | 2000-07-26 | 2002-01-30 | Mitsubishi Polyester Film GmbH | Biaxially oriented white polyester film |
CN1482174A (en) * | 2002-09-10 | 2004-03-17 | 上海紫东化工塑料有限公司 | High transparent polyester film and process for producing the same |
JP2004099659A (en) * | 2002-09-05 | 2004-04-02 | Toray Ind Inc | White aliphatic polyester film and method for producing the same |
CN1500822A (en) * | 2002-11-14 | 2004-06-02 | 仪化集团公司 | Polyester film and producing process thereof |
JP2004202899A (en) * | 2002-12-26 | 2004-07-22 | Mitsubishi Polyester Film Copp | Biaxially stretched laminated polyester film |
CN1554702A (en) * | 2003-12-26 | 2004-12-15 | 四川东方绝缘材料股份有限公司 | Process for producing polyester film for tyre rubber demoulding |
JP4227641B2 (en) * | 2006-11-20 | 2009-02-18 | キヤノン株式会社 | Information processing apparatus and information processing apparatus control method |
-
2008
- 2008-04-07 CN CN 200810023253 patent/CN101260196B/en active Active
Patent Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1176004A1 (en) * | 2000-07-26 | 2002-01-30 | Mitsubishi Polyester Film GmbH | Biaxially oriented white polyester film |
JP2004099659A (en) * | 2002-09-05 | 2004-04-02 | Toray Ind Inc | White aliphatic polyester film and method for producing the same |
CN1482174A (en) * | 2002-09-10 | 2004-03-17 | 上海紫东化工塑料有限公司 | High transparent polyester film and process for producing the same |
CN1500822A (en) * | 2002-11-14 | 2004-06-02 | 仪化集团公司 | Polyester film and producing process thereof |
JP2004202899A (en) * | 2002-12-26 | 2004-07-22 | Mitsubishi Polyester Film Copp | Biaxially stretched laminated polyester film |
CN1554702A (en) * | 2003-12-26 | 2004-12-15 | 四川东方绝缘材料股份有限公司 | Process for producing polyester film for tyre rubber demoulding |
JP4227641B2 (en) * | 2006-11-20 | 2009-02-18 | キヤノン株式会社 | Information processing apparatus and information processing apparatus control method |
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