CN106299006B - A kind of solar cell backboard film and preparation method thereof - Google Patents
A kind of solar cell backboard film and preparation method thereof Download PDFInfo
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- CN106299006B CN106299006B CN201610811774.1A CN201610811774A CN106299006B CN 106299006 B CN106299006 B CN 106299006B CN 201610811774 A CN201610811774 A CN 201610811774A CN 106299006 B CN106299006 B CN 106299006B
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- 238000002360 preparation method Methods 0.000 title claims abstract description 18
- 239000002994 raw material Substances 0.000 claims abstract description 26
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims abstract description 24
- DPXJVFZANSGRMM-UHFFFAOYSA-N acetic acid;2,3,4,5,6-pentahydroxyhexanal;sodium Chemical compound [Na].CC(O)=O.OCC(O)C(O)C(O)C(O)C=O DPXJVFZANSGRMM-UHFFFAOYSA-N 0.000 claims abstract description 13
- 239000001768 carboxy methyl cellulose Substances 0.000 claims abstract description 13
- SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 claims abstract description 13
- 229920000728 polyester Polymers 0.000 claims abstract description 13
- 239000000843 powder Substances 0.000 claims abstract description 13
- 235000019812 sodium carboxymethyl cellulose Nutrition 0.000 claims abstract description 13
- 229920001027 sodium carboxymethylcellulose Polymers 0.000 claims abstract description 13
- 239000004697 Polyetherimide Substances 0.000 claims abstract description 12
- 150000001412 amines Chemical class 0.000 claims abstract description 12
- 239000004611 light stabiliser Substances 0.000 claims abstract description 12
- 229920001495 poly(sodium acrylate) polymer Polymers 0.000 claims abstract description 12
- 229920001601 polyetherimide Polymers 0.000 claims abstract description 12
- 239000000377 silicon dioxide Substances 0.000 claims abstract description 12
- NNMHYFLPFNGQFZ-UHFFFAOYSA-M sodium polyacrylate Chemical compound [Na+].[O-]C(=O)C=C NNMHYFLPFNGQFZ-UHFFFAOYSA-M 0.000 claims abstract description 12
- MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Natural products CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 claims abstract description 11
- GHKOFFNLGXMVNJ-UHFFFAOYSA-N Didodecyl thiobispropanoate Chemical compound CCCCCCCCCCCCOC(=O)CCSCCC(=O)OCCCCCCCCCCCC GHKOFFNLGXMVNJ-UHFFFAOYSA-N 0.000 claims abstract description 11
- 239000003508 Dilauryl thiodipropionate Substances 0.000 claims abstract description 11
- BJQHLKABXJIVAM-UHFFFAOYSA-N bis(2-ethylhexyl) phthalate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC BJQHLKABXJIVAM-UHFFFAOYSA-N 0.000 claims abstract description 11
- 229920005549 butyl rubber Polymers 0.000 claims abstract description 11
- 235000019304 dilauryl thiodipropionate Nutrition 0.000 claims abstract description 11
- ZNRLMGFXSPUZNR-UHFFFAOYSA-N 2,2,4-trimethyl-1h-quinoline Chemical compound C1=CC=C2C(C)=CC(C)(C)NC2=C1 ZNRLMGFXSPUZNR-UHFFFAOYSA-N 0.000 claims abstract description 10
- 229960000686 benzalkonium chloride Drugs 0.000 claims abstract description 10
- CADWTSSKOVRVJC-UHFFFAOYSA-N benzyl(dimethyl)azanium;chloride Chemical compound [Cl-].C[NH+](C)CC1=CC=CC=C1 CADWTSSKOVRVJC-UHFFFAOYSA-N 0.000 claims abstract description 10
- 239000002033 PVDF binder Substances 0.000 claims abstract description 8
- 229920002981 polyvinylidene fluoride Polymers 0.000 claims abstract description 8
- 239000000463 material Substances 0.000 claims abstract description 7
- 239000004594 Masterbatch (MB) Substances 0.000 claims description 14
- 239000000203 mixture Substances 0.000 claims description 14
- 238000005453 pelletization Methods 0.000 claims description 14
- 239000002253 acid Substances 0.000 claims description 11
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims description 9
- NLZUEZXRPGMBCV-UHFFFAOYSA-N Butylhydroxytoluene Chemical compound CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 NLZUEZXRPGMBCV-UHFFFAOYSA-N 0.000 claims description 8
- 235000010354 butylated hydroxytoluene Nutrition 0.000 claims description 8
- 239000011261 inert gas Substances 0.000 claims description 8
- 238000010096 film blowing Methods 0.000 claims description 7
- 239000002985 plastic film Substances 0.000 claims description 7
- 229920006255 plastic film Polymers 0.000 claims description 7
- 238000004804 winding Methods 0.000 claims description 7
- 239000012528 membrane Substances 0.000 claims description 6
- 238000000034 method Methods 0.000 claims description 6
- 239000003795 chemical substances by application Substances 0.000 claims description 2
- 238000003756 stirring Methods 0.000 claims description 2
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 claims 2
- QTWJRLJHJPIABL-UHFFFAOYSA-N 2-methylphenol;3-methylphenol;4-methylphenol Chemical compound CC1=CC=C(O)C=C1.CC1=CC=CC(O)=C1.CC1=CC=CC=C1O QTWJRLJHJPIABL-UHFFFAOYSA-N 0.000 claims 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims 1
- 229920002125 Sokalan® Polymers 0.000 claims 1
- 239000000460 chlorine Substances 0.000 claims 1
- 229910052801 chlorine Inorganic materials 0.000 claims 1
- 150000002989 phenols Chemical class 0.000 claims 1
- 239000004584 polyacrylic acid Substances 0.000 claims 1
- 235000019260 propionic acid Nutrition 0.000 claims 1
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 claims 1
- 239000011734 sodium Substances 0.000 claims 1
- 229910052708 sodium Inorganic materials 0.000 claims 1
- 125000000446 sulfanediyl group Chemical group *S* 0.000 claims 1
- 230000032683 aging Effects 0.000 abstract description 4
- AOJJSUZBOXZQNB-VTZDEGQISA-N 4'-epidoxorubicin Chemical compound O([C@H]1C[C@@](O)(CC=2C(O)=C3C(=O)C=4C=CC=C(C=4C(=O)C3=C(O)C=21)OC)C(=O)CO)[C@H]1C[C@H](N)[C@@H](O)[C@H](C)O1 AOJJSUZBOXZQNB-VTZDEGQISA-N 0.000 abstract description 2
- 230000015556 catabolic process Effects 0.000 abstract description 2
- IWDCLRJOBJJRNH-UHFFFAOYSA-N p-cresol Chemical compound CC1=CC=C(O)C=C1 IWDCLRJOBJJRNH-UHFFFAOYSA-N 0.000 abstract 2
- 230000000052 comparative effect Effects 0.000 description 6
- 230000000694 effects Effects 0.000 description 6
- 238000012423 maintenance Methods 0.000 description 5
- VORLTHPZWVELIX-UHFFFAOYSA-N 1-methyl-2h-quinoline Chemical compound C1=CC=C2N(C)CC=CC2=C1 VORLTHPZWVELIX-UHFFFAOYSA-N 0.000 description 3
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 3
- 238000005516 engineering process Methods 0.000 description 3
- 229910052710 silicon Inorganic materials 0.000 description 3
- 239000010703 silicon Substances 0.000 description 3
- MKYBYDHXWVHEJW-UHFFFAOYSA-N N-[1-oxo-1-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)propan-2-yl]-2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidine-5-carboxamide Chemical compound O=C(C(C)NC(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F)N1CC2=C(CC1)NN=N2 MKYBYDHXWVHEJW-UHFFFAOYSA-N 0.000 description 2
- 239000000853 adhesive Substances 0.000 description 2
- 230000001070 adhesive effect Effects 0.000 description 2
- 230000005540 biological transmission Effects 0.000 description 2
- 238000005260 corrosion Methods 0.000 description 2
- 230000032798 delamination Effects 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 2
- 238000010248 power generation Methods 0.000 description 2
- 230000005855 radiation Effects 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- IRFSXVIRXMYULF-UHFFFAOYSA-N 1,2-dihydroquinoline Chemical compound C1=CC=C2C=CCNC2=C1 IRFSXVIRXMYULF-UHFFFAOYSA-N 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 239000005864 Sulphur Substances 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 238000011056 performance test Methods 0.000 description 1
- 239000005060 rubber Substances 0.000 description 1
- 239000004065 semiconductor Substances 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
Classifications
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J5/00—Manufacture of articles or shaped materials containing macromolecular substances
- C08J5/18—Manufacture of films or sheets
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L25/00—Compositions of, 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 an aromatic carbocyclic ring; Compositions of derivatives of such polymers
- C08L25/18—Homopolymers or copolymers of aromatic monomers containing elements other than carbon and hydrogen
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L27/00—Compositions of 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; Compositions of derivatives of such polymers
- C08L27/02—Compositions of 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; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L27/12—Compositions of 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; Compositions of derivatives of such polymers not modified by chemical after-treatment containing fluorine atoms
- C08L27/16—Homopolymers or copolymers or vinylidene fluoride
-
- 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
- H01L31/18—Processes or apparatus specially adapted for the manufacture or treatment of these devices or of parts thereof
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2325/00—Characterised by the use of 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 an aromatic carbocyclic ring; Derivatives of such polymers
- C08J2325/18—Homopolymers or copolymers of aromatic monomers containing elements other than carbon and hydrogen
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2327/00—Characterised by the use of 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; Derivatives of such polymers
- C08J2327/02—Characterised by the use of 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; Derivatives of such polymers not modified by chemical after-treatment
- C08J2327/12—Characterised by the use of 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; Derivatives of such polymers not modified by chemical after-treatment containing fluorine atoms
- C08J2327/16—Homopolymers or copolymers of vinylidene fluoride
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2425/00—Characterised by the use of 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 an aromatic carbocyclic ring; Derivatives of such polymers
- C08J2425/18—Homopolymers or copolymers of aromatic monomers containing elements other than carbon and hydrogen
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2201/00—Properties
- C08L2201/08—Stabilised against heat, light or radiation or oxydation
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2201/00—Properties
- C08L2201/14—Gas barrier composition
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2203/00—Applications
- C08L2203/16—Applications used for films
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2203/00—Applications
- C08L2203/20—Applications use in electrical or conductive gadgets
- C08L2203/206—Applications use in electrical or conductive gadgets use in coating or encapsulating of electronic parts
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2205/00—Polymer mixtures characterised by other features
- C08L2205/03—Polymer mixtures characterised by other features containing three or more polymers in a blend
- C08L2205/035—Polymer mixtures characterised by other features containing three or more polymers in a blend containing four or more polymers in a blend
-
- 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
-
- 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
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P70/00—Climate change mitigation technologies in the production process for final industrial or consumer products
- Y02P70/50—Manufacturing or production processes characterised by the final manufactured product
Abstract
The invention discloses a kind of solar cell backboard film and preparation method thereof, the solar cell backboard film is made of the raw material of following parts by weight:12 20 parts of butyl rubber, 20 32 parts of Kynoar PVDF, 4 10 parts of dipropylene glycol, 12 24 parts of polyester powder, 28 parts of Sodium Polyacrylate, 4 10 parts of benzalkonium chloride, 20 30 parts of polystyrolsulfon acid, 8 14 parts of silica, 6 10 parts of polyetherimide, 28 parts of 2,6 di-t-butyl, 4 methylphenol, 6 12 parts of sodium carboxymethylcellulose, 17 parts of poly- trimethyldihydroquinoline, 0.2 0.8 parts of dilauryl thiodipropionate, 15 parts of hindered amine light stabilizer, 0.6 1.8 parts of dioctyl phthalate;The solar cell backboard film of gained of the invention can effectively extend solar energy backboard service life, enhance that solar energy backboard is heat-resisting, ageing-resistant, vapour resistant through performance, it with higher breakdown voltage property, and can completely be bonded together, be not easily stripped with base material;It has a extensive future.
Description
Technical field
The present invention relates to solar cell material preparing technical field, specifically a kind of solar cell backboard film and its system
Preparation Method.
Background technology
Earth environment pollutes and energy shortage problem is on the rise, and solar cell power generation is to solve both of these problems most
One of effective way;Solar power generation is that directly the visible light of the sun is changed into using the quantum effect principle of the semiconductors such as silicon
Electric energy, but since it faces atrocious weather, it would be desirable to which a kind of material protects silicon chip of solar cell, straight in face of the sun
We generally protect silicon chip to the one side penetrated using glass, and reverse side then needs to protect using solar battery back film;The sun
The notacoria of energy battery component is located at the back side of solar panel, and protection and supporting role, solar cell are played to cell piece
The notacoria of component plays a key effect to battery, output power, security reliability;And the notacoria of the prior art is weather-proof
Property, water preventing ability, insulating properties and resistance to ag(e)ing it is poor, can not ensure that battery is reliable, stablize, use safely for a long time, influence property
Energy and service life increase maintenance cost, therefore, there is an urgent need to propose new solar cell backboard membrane technology, in solution
State problem.
Invention content
The purpose of the present invention is to provide a kind of of low cost, simple for process, weatherability, water preventing ability, ageing-resistant performance are good
Solar cell backboard film and preparation method thereof, to solve the problems mentioned in the above background technology.
To achieve the above object, the present invention provides the following technical solutions:
A kind of solar cell backboard film, is made of the raw material of following parts by weight:12-20 parts of butyl rubber, polyvinylidene fluoride
20-32 parts of alkene PVDF, 4-10 parts of dipropylene glycol, 12-24 parts of polyester powder, 2-8 parts of Sodium Polyacrylate, 4-10 parts of benzalkonium chloride,
20-30 parts of polystyrolsulfon acid, 8-14 parts of silica, 6-10 parts of polyetherimide, 2,6 di tert butyl 4 methyl phenol 2-
8 parts, 6-12 parts of sodium carboxymethylcellulose, trimethyldihydroquinoline 1-7 parts poly-, 0.2-0.8 parts of dilauryl thiodipropionate, by
Hinder 1-5 parts of amine light stabilizer, 0.6-1.8 parts of dioctyl phthalate.
As a further solution of the present invention:The solar cell backboard film, is made of the raw material of following parts by weight:Fourth
14-18 parts of base rubber, 24-28 parts of Kynoar PVDF, 6-8 parts of dipropylene glycol, 16-20 parts of polyester powder, Sodium Polyacrylate
4-6 parts, 5-9 parts of benzalkonium chloride, 23-27 parts of polystyrolsulfon acid, 0-12 parts of silica 1,7-9 parts of polyetherimide, 2,6-
4-6 parts of di-tert-butyl-4-methy phenol, 8-10 parts of sodium carboxymethylcellulose, trimethyldihydroquinoline 3-5 parts poly-, thio dipropyl
Sour dilauryl 0.4-0.6 parts, 2-4 parts of hindered amine light stabilizer, 1-1.4 parts of dioctyl phthalate.
As further scheme of the invention:The solar cell backboard film, is made of the raw material of following parts by weight:
16 parts of butyl rubber, 26 parts of Kynoar PVDF, 7 parts of dipropylene glycol, 18 parts of polyester powder, 5 parts of Sodium Polyacrylate, benzene are pricked
7 parts of oronain, 25 parts of polystyrolsulfon acid, 1 part of silica 1,8 parts of polyetherimide, 2,6 di tert butyl 4 methyl phenol 5
Part, 9 parts of sodium carboxymethylcellulose, 4 parts of poly- trimethyldihydroquinoline, 0.5 part of dilauryl thiodipropionate, hindered amine light stabilizer
3 parts of agent, 1.2 parts of dioctyl phthalate.
As further scheme of the invention:The preparation method of the solar cell backboard film, including following step
Suddenly:
1) dispensing:Each raw material for standby is weighed by formula;
2) it is stirred:The raw material weighed is added in reaction kettle and is uniformly mixed, whipping temp 120-160
DEG C, mixing speed 200-300r/min, mixing time 60-80min obtain mixture;
3) extruding pelletization:The mixture of gained in step 2) is put into comminutor, point four sections of temperature extruding pelletizations obtain
Form a film masterbatch;
4) blown film is wound:The film forming masterbatch obtained in step 3) is squeezed out into blown film using plastic film blowing machine, obtains solar energy
Battery back-sheet film, winding, storage.
As further scheme of the invention:In the step 2), indifferent gas is filled in whipping process into reaction kettle
Body makes material stir under inert gas protection.
As further scheme of the invention:In the step 3), first segment temperature is 200-210 DEG C, second segment temperature
Degree is 210-220 DEG C, and third section temperature is 220-240 DEG C, and the 4th section of temperature is 230-250 DEG C.
Compared with prior art, the beneficial effects of the invention are as follows:Solar cell backboard film of the invention is of low cost, makes
It is standby simple for process, have excellent anti-aqueous vapor effect and weatherability, anti-corrosion effects good;It can completely be bonded in one with base material
It rises, adhesive ability is strong, and backboard membrane is unlikely to deform or delamination, is not easily stripped, and can effectively extend solar energy backboard and use the longevity
Life reduces maintenance maintenance cost, enhances that solar energy backboard is heat-resisting, ageing-resistant, vapour resistant through performance, and ductility is high, hits
Voltage strength height is worn, shelf depreciation voltage is high, has extremely strong application prospect.
Specific implementation mode
The technical solution of this patent is described in more detail With reference to embodiment.
Embodiment 1
A kind of solar cell backboard film, is made of the raw material of following parts by weight:12 parts of butyl rubber, Kynoar
PVDF20 parts, 4 parts of dipropylene glycol, 12 parts of polyester powder, 2 parts of Sodium Polyacrylate, 4 parts of benzalkonium chloride, 20 parts of polystyrolsulfon acid,
8 parts of silica, 6 parts of polyetherimide, 2 parts of 2,6 di tert butyl 4 methyl phenol, 6 parts of sodium carboxymethylcellulose, poly- front three
1 part of base dihydroquinoline, 0.2 part of dilauryl thiodipropionate, 1 part of hindered amine light stabilizer, dioctyl phthalate 0.6
Part.
The preparation method of the solar cell backboard film, includes the following steps:
1) dispensing:Each raw material for standby is weighed by formula;
2) it is stirred:The raw material weighed is added in reaction kettle and is uniformly mixed under inert gas protection,
Whipping temp is 120 DEG C, mixing speed 200r/min, mixing time 60min and obtains mixture;
3) extruding pelletization:The mixture of gained in step 2) is put into comminutor, point four sections of temperature extruding pelletizations, first
Duan Wendu is 200-210 DEG C, and second segment temperature is 210-220 DEG C, and third section temperature is 220-240 DEG C, and the 4th section of temperature is
230-250℃;Obtain film forming masterbatch;
4) blown film is wound:The film forming masterbatch obtained in step 3) is squeezed out into blown film using plastic film blowing machine, obtains solar energy
Battery back-sheet film, winding, storage.
Embodiment 2
A kind of solar cell backboard film, is made of the raw material of following parts by weight:20 parts of butyl rubber, Kynoar
PVDF32 parts, 10 parts of dipropylene glycol, 24 parts of polyester powder, 8 parts of Sodium Polyacrylate, 10 parts of benzalkonium chloride, polystyrolsulfon acid 30
Part, 4 parts of silica 1,10 parts of polyetherimide, 8 parts of 2,6 di tert butyl 4 methyl phenol, 12 parts of sodium carboxymethylcellulose,
7 parts of poly- trimethyldihydroquinoline, 0.8 part of dilauryl thiodipropionate, 5 parts of hindered amine light stabilizer, phthalic acid two are pungent
1.8 parts of ester.
The preparation method of the solar cell backboard film, includes the following steps:
1) dispensing:Each raw material for standby is weighed by formula;
2) it is stirred:The raw material weighed is added in reaction kettle and is uniformly mixed under inert gas protection,
Whipping temp is 130 DEG C, mixing speed 220r/min, mixing time 65min and obtains mixture;
3) extruding pelletization:The mixture of gained in step 2) is put into comminutor, point four sections of temperature extruding pelletizations, first
Duan Wendu is 200-210 DEG C, and second segment temperature is 210-220 DEG C, and third section temperature is 220-240 DEG C, and the 4th section of temperature is
230-250℃;Obtain film forming masterbatch;
4) blown film is wound:The film forming masterbatch obtained in step 3) is squeezed out into blown film using plastic film blowing machine, obtains solar energy
Battery back-sheet film, winding, storage.
Embodiment 3
A kind of solar cell backboard film, is made of the raw material of following parts by weight:14 parts of butyl rubber, Kynoar
PVDF24 parts, 6 parts of dipropylene glycol, 16 parts of polyester powder, 4 parts of Sodium Polyacrylate, 5 parts of benzalkonium chloride, 23 parts of polystyrolsulfon acid,
0 part of silica 1,7 parts of polyetherimide, 4 parts of 2,6 di tert butyl 4 methyl phenol, 8 parts of sodium carboxymethylcellulose, poly- three
3 parts of methyl dihydroquinoline, 0.4 part of dilauryl thiodipropionate, 2 parts of hindered amine light stabilizer, dioctyl phthalate 1
Part.
The preparation method of the solar cell backboard film, includes the following steps:
1) dispensing:Each raw material for standby is weighed by formula;
2) it is stirred:The raw material weighed is added in reaction kettle and is uniformly mixed under inert gas protection,
Whipping temp is 140 DEG C, mixing speed 240r/min, mixing time 70min and obtains mixture;
3) extruding pelletization:The mixture of gained in step 2) is put into comminutor, point four sections of temperature extruding pelletizations, first
Duan Wendu is 200-210 DEG C, and second segment temperature is 210-220 DEG C, and third section temperature is 220-240 DEG C, and the 4th section of temperature is
230-250℃;Obtain film forming masterbatch;
4) blown film is wound:The film forming masterbatch obtained in step 3) is squeezed out into blown film using plastic film blowing machine, obtains solar energy
Battery back-sheet film, winding, storage.
Embodiment 4
A kind of solar cell backboard film, is made of the raw material of following parts by weight:18 parts of butyl rubber, Kynoar
PVDF28 parts, 8 parts of dipropylene glycol, 20 parts of polyester powder, 6 parts of Sodium Polyacrylate, 9 parts of benzalkonium chloride, 27 parts of polystyrolsulfon acid,
2 parts of silica 1,9 parts of polyetherimide, 6 parts of 2,6 di tert butyl 4 methyl phenol, 10 parts of sodium carboxymethylcellulose, poly- three
5 parts of methyl dihydroquinoline, 0.6 part of dilauryl thiodipropionate, 4 parts of hindered amine light stabilizer, dioctyl phthalate 1.4
Part.
The preparation method of the solar cell backboard film, includes the following steps:
1) dispensing:Each raw material for standby is weighed by formula;
2) it is stirred:The raw material weighed is added in reaction kettle and is uniformly mixed under inert gas protection,
Whipping temp is 150 DEG C, mixing speed 260r/min, mixing time 75min and obtains mixture;
3) extruding pelletization:The mixture of gained in step 2) is put into comminutor, point four sections of temperature extruding pelletizations, first
Duan Wendu is 200-210 DEG C, and second segment temperature is 210-220 DEG C, and third section temperature is 220-240 DEG C, and the 4th section of temperature is
230-250℃;Obtain film forming masterbatch;
4) blown film is wound:The film forming masterbatch obtained in step 3) is squeezed out into blown film using plastic film blowing machine, obtains solar energy
Battery back-sheet film, winding, storage.
Embodiment 5
A kind of solar cell backboard film, is made of the raw material of following parts by weight:16 parts of butyl rubber, Kynoar
PVDF26 parts, 7 parts of dipropylene glycol, 18 parts of polyester powder, 5 parts of Sodium Polyacrylate, 7 parts of benzalkonium chloride, 25 parts of polystyrolsulfon acid,
1 part of silica 1,8 parts of polyetherimide, 5 parts of 2,6 di tert butyl 4 methyl phenol, 9 parts of sodium carboxymethylcellulose, poly- three
4 parts of methyl dihydroquinoline, 0.5 part of dilauryl thiodipropionate, 3 parts of hindered amine light stabilizer, dioctyl phthalate 1.2
Part.
The preparation method of the solar cell backboard film, includes the following steps:
1) dispensing:Each raw material for standby is weighed by formula;
2) it is stirred:The raw material weighed is added in reaction kettle and is uniformly mixed under inert gas protection,
Whipping temp is 140 DEG C, mixing speed 250r/min, mixing time 70min and obtains mixture;
3) extruding pelletization:The mixture of gained in step 2) is put into comminutor, point four sections of temperature extruding pelletizations, first
Duan Wendu is 200-210 DEG C, and second segment temperature is 210-220 DEG C, and third section temperature is 220-240 DEG C, and the 4th section of temperature is
230-250℃;Obtain film forming masterbatch;
4) blown film is wound:The film forming masterbatch obtained in step 3) is squeezed out into blown film using plastic film blowing machine, obtains solar energy
Battery back-sheet film, winding, storage.
Comparative example 1
Using the formula of embodiment 5, the difference is that being prepared without poly- trimethyldihydroquinoline and Sodium Polyacrylate in formula
Method is same as Example 5 with step.
Comparative example 2
Using the formula of embodiment 5, the difference is that being prepared without dipropylene glycol and dilauryl thiodipropionate in formula
Method is same as Example 5 with step.
Comparative example 3
Using the formula of embodiment 5, unlike in formula without polyester powder and benzalkonium chloride, preparation method and step
It is same as Example 5.
Comparative example 4
Using the formula of embodiment 5, the difference is that without sodium carboxymethylcellulose, poly- trimethyldihydroquinoline and sulphur in formula
For dipropionic acid dilauryl, preparation method is same as Example 5 with step.
Experimental example 1
The obtained solar energy backboard membranes of embodiment 1-5 and comparative example 1-4 are carried out about tensile strength, extension at break
The performance test of degree, peel strength, shelf depreciation and yellowness index, test result is as follows shown in table 1:
Table 1
The items that solar cell backboard film obtained by embodiment 5 known to from upper table 1 is tested in all embodiments
Data are optimal, and the solar cell backboard that the formula of embodiment 5 is prepared can be obtained when compared with comparative example 1-4
Film properties are optimal, formula it is the most reasonable, have significant performance improve, tensile strength, extension at break degree, peel strength,
Clear superiority is all had in shelf depreciation and yellowness index properties.
Experimental example 2
Using the solar cell backboard film obtained by 1-5 of the embodiment of the present invention as experimental group, with backboard membrane common on the market
For control group, it is as shown in table 2 below that vapor transmission, man-made radiation and thermal deformation experiment, the result of gained are carried out respectively:
Table 2
1-5 of embodiment of the present invention resulting products are in vapor transmission, man-made radiation and thermal deformation experiment as seen from the above table
Aspect is significantly better than solar cell backboard film common on the market;The present invention solar cell backboard film it is of low cost,
Preparation process is simple, has excellent anti-aqueous vapor effect and weatherability, anti-corrosion effects good;It can be completely bonded in base material
Together, adhesive ability is strong, and backboard membrane is unlikely to deform or delamination, is not easily stripped, and can effectively extend the use of solar energy backboard
Service life reduces maintenance maintenance cost, enhances that solar energy backboard is heat-resisting, ageing-resistant, vapour resistant through performance, and ductility is high,
Breakdown voltage strength is high, and shelf depreciation voltage is high, has extremely strong application prospect.
It is obvious to a person skilled in the art that invention is not limited to the details of the above exemplary embodiments, Er Qie
In the case of without departing substantially from spirit or essential attributes of the invention, the present invention can be realized in other specific forms.Therefore, no matter
From the point of view of which point, the present embodiments are to be considered as illustrative and not restrictive, and the scope of the present invention is by appended power
Profit requires rather than above description limits, it is intended that all by what is fallen within the meaning and scope of the equivalent requirements of the claims
Variation is included within the present invention.
In addition, it should be understood that although this specification is described in terms of embodiments, but not each embodiment is only wrapped
Containing an independent technical solution, this description of the specification is merely for the sake of clarity, and those skilled in the art should
It considers the specification as a whole, the technical solutions in the various embodiments may also be suitably combined, forms those skilled in the art
The other embodiment being appreciated that.
Claims (6)
1. a kind of solar cell backboard film, it is characterised in that:It is made of the raw material of following parts by weight:12-20 parts of butyl rubber,
20-32 parts of Kynoar PVDF, 4-10 parts of dipropylene glycol, 12-24 parts of polyester powder, 2-8 parts of Sodium Polyacrylate, benzene prick chlorine
4-10 parts of ammonium, 20-30 parts of polystyrolsulfon acid, 8-14 parts of silica, 6-10 parts of polyetherimide, 2,6- di-t-butyls -4-
2-8 parts of methylphenol, 6-12 parts of sodium carboxymethylcellulose, trimethyldihydroquinoline 1-7 parts poly-, dilauryl thiodipropionate
0.2-0.8 parts, 1-5 parts of hindered amine light stabilizer, 0.6-1.8 parts of dioctyl phthalate.
2. solar cell backboard film according to claim 1, which is characterized in that be made of the raw material of following parts by weight:
14-18 parts of butyl rubber, 24-28 parts of Kynoar PVDF, 6-8 parts of dipropylene glycol, 16-20 parts of polyester powder, polyacrylic acid
4-6 parts of sodium, 5-9 parts of benzalkonium chloride, 23-27 parts of polystyrolsulfon acid, 0-12 parts of silica 1,7-9 parts of polyetherimide, 2,
4-6 parts of 6- di-tert-butyl-4-methy phenols, 8-10 parts of sodium carboxymethylcellulose, it is trimethyldihydroquinoline 3-5 parts poly-, thio two
0.4-0.6 parts of propionic acid dilauryl, 2-4 parts of hindered amine light stabilizer, 1-1.4 parts of dioctyl phthalate.
3. solar cell backboard film according to claim 1, which is characterized in that be made of the raw material of following parts by weight:
16 parts of butyl rubber, 26 parts of Kynoar PVDF, 7 parts of dipropylene glycol, 18 parts of polyester powder, 5 parts of Sodium Polyacrylate, benzene are pricked
7 parts of oronain, 25 parts of polystyrolsulfon acid, 1 part of silica 1,8 parts of polyetherimide, 2,6 di tert butyl 4 methyl phenol 5
Part, 9 parts of sodium carboxymethylcellulose, 4 parts of poly- trimethyldihydroquinoline, 0.5 part of dilauryl thiodipropionate, hindered amine light stabilizer
3 parts of agent, 1.2 parts of dioctyl phthalate.
4. a kind of preparation method of solar cell backboard film as described in any one of claims 1-3, which is characterized in that including with
Lower step:
1) dispensing:Each raw material for standby is weighed by formula;
2) it is stirred:The raw material weighed is added in reaction kettle and is uniformly mixed, whipping temp is 120-160 DEG C,
Mixing speed is 200-300r/min, and mixing time 60-80min obtains mixture;
3) extruding pelletization:The mixture of gained in step 2) is put into comminutor, point four sections of temperature extruding pelletizations are formed a film
Masterbatch;
4) blown film is wound:The film forming masterbatch obtained in step 3) is squeezed out into blown film using plastic film blowing machine, obtains solar cell
Backboard membrane, winding, storage.
5. the preparation method of solar cell backboard film according to claim 4, which is characterized in that in the step 2),
Inert gas is filled in whipping process into reaction kettle, material is made to stir under inert gas protection.
6. the preparation method of solar cell backboard film according to claim 5, which is characterized in that in the step 3),
First segment temperature is 200-210 DEG C, and second segment temperature is 210-220 DEG C, and third section temperature is 220-240 DEG C, the 4th section of temperature
It is 230-250 DEG C.
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CN103943723A (en) * | 2014-04-03 | 2014-07-23 | 安徽金兑新材料科技有限公司 | High-performance solar cell backboard film manufacturing process |
CN104327428A (en) * | 2014-11-13 | 2015-02-04 | 无锡中洁能源技术有限公司 | Nano-silicon modified polyvinylidene fluoride solar cell back film material and preparation method thereof |
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CN102067328A (en) * | 2008-06-26 | 2011-05-18 | 三井-杜邦聚合化学株式会社 | Laminated sheet for solar cell, and solar cell module comprising the same |
KR102009136B1 (en) * | 2011-07-13 | 2019-08-09 | 덴카 주식회사 | Vinylidene fluoride resin composition, resin film, back sheet for solar cells, and solar cell module |
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CN104356548A (en) * | 2014-11-13 | 2015-02-18 | 无锡中洁能源技术有限公司 | High-light transmittance photovoltaic solar cell packaging film and preparation method thereof |
CN104371285B (en) * | 2014-11-14 | 2016-06-08 | 无锡中洁能源技术有限公司 | A kind of high temperature resistant light aging resisting solar cell backboard film and preparation method thereof |
CN104449519A (en) * | 2014-12-31 | 2015-03-25 | 明冠新材料股份有限公司 | Glue for combining solar cell backboard film and PE film and preparing method of glue |
CN104966754B (en) * | 2015-06-30 | 2017-03-01 | 杭州福斯特光伏材料股份有限公司 | A kind of solar module high water resistant backboard |
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CN103943723A (en) * | 2014-04-03 | 2014-07-23 | 安徽金兑新材料科技有限公司 | High-performance solar cell backboard film manufacturing process |
CN104327428A (en) * | 2014-11-13 | 2015-02-04 | 无锡中洁能源技术有限公司 | Nano-silicon modified polyvinylidene fluoride solar cell back film material and preparation method thereof |
CN104388002A (en) * | 2014-11-13 | 2015-03-04 | 无锡中洁能源技术有限公司 | Solar cell light conversion packaging adhesive film and preparation method thereof |
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