CN105006497B - High pressure backboard is used in a kind of crystal silicon component encapsulation - Google Patents
High pressure backboard is used in a kind of crystal silicon component encapsulation Download PDFInfo
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- CN105006497B CN105006497B CN201510373313.6A CN201510373313A CN105006497B CN 105006497 B CN105006497 B CN 105006497B CN 201510373313 A CN201510373313 A CN 201510373313A CN 105006497 B CN105006497 B CN 105006497B
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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
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- 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
Abstract
The present invention relates to high pressure backboard is used in a kind of crystal silicon component encapsulation, belong to photovoltaic encapsulation Material Field.The backboard is made up of base layer, the weather-proof outer layer of crosslinking fluororesin in the middle of modified olefin internal layer, polyester.Obtained in of the invention, backboard has very high shelf depreciation pressure, while also having good water vapor barrier property and excellent mechanical strength and outdoor weathe resistance.Preparation technology of the present invention is easy, and properties of product are stable, apply to the outstanding photovoltaic back of big system crystal silicon component.
Description
Technical field
The present invention relates to high pressure backboard is used in a kind of crystal silicon component encapsulation, belong to photovoltaic encapsulation Material Field.
Background technology
Photovoltaic generating system is the electricity generation system that electric energy is directly converted solar energy into using solar cell.It main
Feature be reliability height, long service life, it is free from environmental pollution, can Independent Power Generation can be incorporated into the power networks again, thus by every industry or trade
The favor of tissue, with vast potential for future development.
From 19 century 70s, the photovoltaic module of carrying photovoltaic generation Main Function is developed so far and has nearly 40 years
Course, with science and technology continuous development and innovation crystal silicon component with its high electricity conversion, high cost performance with
And the production technology of maturation gradually occupies the share of photovoltaic module more than 80%.But, the cost of former auxiliary material remains obstruction
The popular biggest obstacle of photovoltaic generation.Nearly 2 years, based on the usage amount that can both drop some former auxiliary materials, unit can be increased again
The big system component development of the higher price-performance ratio of the photovoltaic power generation quantity on area is quick.Technical staff in industry, actively
Assessment and improvement increase system, for the requirement standard of raw and auxiliary material.
From in composition structure, crystal silicon solar battery component is typically by low iron safety glass, front layer EVA film, monolithic sun electricity
Pond piece, rear layer EVA film and backboard are constituted.Part of its dorsulum as isolation cell piece and ectocine, no matter in weatherability
Aspect still is required for providing reliable guaranteeing role in terms of insulating properties.In terms of insulating properties, common crystal silicon component only will
Ask backboard to reach 1000VDC offices electric discharge pressure and can reach the requirement of insulating properties, and for larger system photovoltaic module simultaneously
It is inapplicable.Big system component is higher than 1500VDC to resistance to office's electric discharge pressure request of photovoltaic back, and according to its cell piece number can
Regulated and controled.In addition to the guarantee in terms of insulating properties, in terms of back board structure stability, water preventing ability, weatherability, it is also desirable to have
Long-term reliability.
Therefore, a class is developed with higher shelf depreciation voltage, there is more excellent adhesive property, mechanical performance, water again
Vapour barrier and the performance such as ageing-resistant, while preparation technology is convenient and photovoltaic back of stable performance is solar cell package row
Industry solves the problem that big system component supplementary material is most urgently solved.
The content of the invention
The invention aims to make up the deficiencies in the prior art, there is provided high pressure backboard is used in a kind of crystal silicon component encapsulation,
This backboard has very high shelf depreciation voltage, and the insulating properties for being adapted to big system photovoltaic module is required, while in bonding
Property, the aspect such as mechanical performance, water vapor barrier property and weatherability also there is good long-term reliability.
The purpose of the present invention is achieved through the following technical solutions:High pressure backboard is used in a kind of crystal silicon component encapsulation, successively
It is made up of base layer in the middle of modified olefin internal layer, polyester and the weather-proof outer layer of crosslinking fluororesin;The modified olefin internal layer thickness is
100~1000 μm, by the first matrix resin, 0.1~10% modified additive A that mass fraction is 65%~95%, 0.1~
10% modified additive B, 0~30% inorganic filler, 0.001%~0.1% ultraviolet absorber, 0.001%~0.1%
Light stabilizer, 0.001%~0.1% thermo oxidative aging agent, 0.01%~5% initiator composition, the first main body tree
Fat is propylene, butylene, heptene, octene, ENB, vinylacetate, methyl acrylate, the one kind in methyl methacrylate
Or two kinds of monomers form olefin copolymer according to any proportioning copolymerization with ethene;In the middle of the polyester matrix ligament thickness be 50~
300 μm, by the second matrix resin, 0~15% inorganic filler that mass fraction is 80%~95%, 0.1%~8% hydrolysis
Stabilizer, 0.01%~3% thermo oxidative aging agent be well mixed after after 250-260 DEG C of melt-processed, it is Jing casting film-formings, double
It is obtained to stretching;Second matrix resin is by polyethylene terephthalate, polybutylene terephthalate (PBT), poly- naphthalene two
One or more in formic acid glycol ester, PBN is constituted according to any proportioning;The crosslinking fluororesin
Weather-proof outer layer thickness is 5~50 μm, inorganic is filled out by the 3rd matrix resin that mass fraction is 70%~90%, 5%~20%
Material, 1%~15% crosslinking agent, 0.001%~1% catalyst composition, the 3rd matrix resin is fluororesin, by hydroxyl
The poly- trifluoro-ethylene ester type fluorocarbon resin of poly- trifluoro-ethylene ether type fluorocarbon resin, hydroxyl, hydroxyl polytetrafluoroethylene (PTFE) ether type fluorocarbon resin,
One or more in hydroxyl polytetrafluoroethylene (PTFE) ester type fluorocarbon resin is constituted according to any proportioning.
Further, the modified additive A is one or several following mixtures constituted according to any proportioning:Acrylic acid
Hydroxyl methyl esters, hydroxy-ethyl acrylate, hydroxypropyl acrylate, 4- hydroxyl ester butyl propyleneglycol acid esters, ethoxy caprolactone acrylic acid, methyl-prop
Olefin(e) acid hydroxyl methyl esters, hydroxyethyl methacrylate, hydroxy propyl methacrylate, 4- hydroxyl ester butyl methyl acrylate, ethoxy oneself
Lactone methacrylic acid, acrylate, acrylic acid diethylamino ethyl ester, acrylic acid tert-butylamino second
Ester, urine base acrylate, dimethylaminoethyl methacrylate, diethyl aminoethyl methacrylate, methacrylic acid
T-butylaminoethyl, urine methyl acrylate;The modified additive B is constituted according to any proportioning for one or several following
Mixture:Silane grafted polyethylene, maleic anhydride grafted polyethylene, glycidyl methacrylate graft polyethylene, third
Acrylamide grafted polyethylene;Described fluororesin is one or several following mixtures constituted according to any proportioning.
Further, the inorganic filler is one or several following mixtures constituted according to any proportioning:Talcum powder,
Calcined kaolin, montmorillonite, mica powder, titanium dioxide, calcium carbonate, barium sulfate, magnesium silicate, aluminium hydroxide, magnesium hydroxide, carbonization
Silicon, copper-chrome black, siderochrome are black, carbon black;
Further, the initiator is one or several following mixtures constituted according to any proportioning:Benzoyl peroxide
Double (benzoyl the peroxide)-hexanes of formyl, 2,5- dimethyl -2,5-, 3,3- double (t-butyl peroxy) ethyl butyrate, neighbours, o- uncle penta
Base-o- (2- ethylhexyls)-mono--peroxycarbonates, neighbour, the o- tert-butyl group-o- isopropyl-mono--peroxycarbonates, neighbour,
The o- tert-butyl group-o- (2- ethylhexyls)-mono--peroxycarbonates, normal-butyl 4,4- bis- (tert-butyl peroxide) valerate, 2,
Double (the t-butyl peroxy)-hexanes of 5- dimethyl -2,5-;
Further, the ultraviolet absorber is one or several following mixtures constituted according to any proportioning:2- hydroxyls
Base -4- methoxy benzophenones, UV-531,2,4 dihydroxyl benzophenone, 2,2,4- trihydroxies
Benzophenone, 2- (2 '-hydroxyl -3 '-the tert-butyl group -5 '-aminomethyl phenyl) -5- chloro benzo triazoles, 2- (2 '-hydroxyl -3 ', 5 ' -
Di-t-butyl -5 '-aminomethyl phenyl) -5- chloro benzo triazoles, 3- [3- (2-H- BTA -2- bases) the tertiary fourths of -4- hydroxyl -5-
Base phenyl]-propionic acid-macrogol ester, 2- (2H- BTA -2- bases) -6- dodecyl -4- methylphenols, 2- (2'- hydroxyls
Base -5'- t-octyl phenyl) BTA, 2- (4,6- double (2,4- 3,5-dimethylphenyls) -1,3,5- triazine -2- bases) -5- octyloxies
Phenol, 2- [4- [2- hydroxyl -3- tridecane epoxide propyl group] epoxide] -2- hydroxy phenyls] double (the 2,4- 3,5-dimethylphenyls) -1 of -4,6-,
3,5- triazines, 2- [4- [2- hydroxyl -3- dodecyloxy propyl group] epoxide] -2- hydroxy phenyls] double (the 2,4- dimethyl benzenes of -4,6-
Base) -1,3,5- triazines;
Further, the light stabilizer is one or several following mixtures constituted according to any proportioning:Double (1,2,
2,6,6- pentamethyl -4- piperidyls)-sebacate/mono- (1,2,2,6,6- pentamethyl -4- piperidyls) sebacate compound,
Bis(2,2,6,6-tetramethyl-4-piperidyl)sebacate, poly- { [6- [(1,1,3,3- tetramethyl butyls) amino]] -1,3,5-
Triazine -2,4- [(2,2,6,6,-tetramethyl-4-piperidyl) imido, double (1- octyloxy -2,2,6,6- tetramethyl -4- piperidyls) last of the ten Heavenly stems
Two acid esters, 2,2,6,6- tetramethyl -4- piperidines stearates, poly-succinic (4- hydroxyl -2,2,6,6- tetramethyl -1- piperidines second
Alcohol) ester;
Further, the thermo oxidative aging agent is one or several following mixtures constituted according to any proportioning:Four
(3,5- di-t-butyl -4- hydroxyls) benzenpropanoic acid pentaerythritol ester, β-positive 18 carbon of (3,5- di-tert-butyl-hydroxy phenyls) propionic acid
Alcohol ester, 2'- di-2-ethylhexylphosphine oxides-(4- methyl-6-tert-butylphenols), three (3,5- di-t-butyl -4- of 1,3,5- trimethyls -2,4,6-
Hydroxybenzyl) benzene, triethylene glycol ether-two (3- tertiary butyl-4-hydroxy -5- aminomethyl phenyls) propionic ester, tri- (the tertiary fourths of 4- of 1,3,5-
Base -3- hydroxyl -2,6- dimethyl benzyls) -1,3,5- triazine -2,4,6- (1H, 3H, 5H)-triketone, three (2,4- bis- of phosphorous acid
Tert-butyl-phenyl) ester, double (2,4- di-tert-butyl-phenyls) pentaerythritol diphosphites, double (2,6- di-t-butyl -4- methylbenzenes
Base) pentaerythritol diphosphate, double four oxygen -3,9- hosphospiros [5.5] hendecanes of octadecane epoxide -2,4,8,10- of 3,9-, 9,
Miscellaneous -10- phospho hetero phenanthrenes -10- the oxides of 10- dihydro-9-oxies, the split isopropyl diphenyl base C12-15- alcohol phosphite esters of 4,4'-;
Further, the hydrolysis stabilizer is one or several following mixtures constituted according to any proportioning:Monomer
Carbodiimides hydrolysis stabilizer, polycarbodiimide class hydrolysis stabilizer, monocarboxylic glycidol hydrolysis of lipid are steady
Determine agent;
Further, the crosslinking agent is one or several following mixtures constituted according to any proportioning:Hexa-methylene
Diisocyanate trimer, hexamethylene diisocyanate prepolymer, isophorone diisocyanate trimer, isophorone two
The many melamine methylol resins of isocyanate prepolymer, methyl-etherified, many melamine methylol resins of butyl etherization, mixed etherificate are more
Melamine methylol resin;
Further, the catalyst is one or several following mixtures constituted according to any proportioning:Stannous octoate,
Tin dilaurate dioctyl tin, monobutyltin oxide, three isooctyl acid tin of monobutyl, dibutyl tin laurate, acetic acid, to toluene sulphur
Acid, phthalic acid, laurate, isooctyl acid.
The raw materials used commercially available acquisition of the present invention.Intermediate layer in three-decker can be by high temperature melting well known in the art
Melt blending after extrusion and stretch processes be obtained, internal layer can by melting casting film-forming after fit to intermediate layer together with make
, then using elder generation, Jing after wet coating, thermal curing methods are obtained outer layer again.
The beneficial effects are mainly as follows:By easy production technology, produce suitable for big system crystal silicon
Component high pressure photovoltaic back;The backboard had both had high shelf depreciation voltage, was adapted to the insulation of big system photovoltaic module
Property require, while at aspects such as caking property, mechanical performance, water vapor barrier property and weatherabilities with excellent combination property, energy
The protective effect in the crystal silicon component of big system to whole component of photovoltaic back is played enough, it is ensured that component is reliably and with long-term
Property.
Description of the drawings
Fig. 1 is a kind of profile of crystal silicon component encapsulation high pressure backboard of the invention.Wherein, 1 is modified olefin internal layer, 2
It is base layer in the middle of polyester, 3 is the weather-proof outer layer of crosslinking fluororesin.
Specific embodiment
With reference to embodiment, the invention will be further described, but protection scope of the present invention is not only limited to implement
Example.
It should be noted that the property indices of photovoltaic back are being measured by following method:
1. shelf depreciation voltage
Method of testing reference standard IEC 61730《Photovoltaic (PV) component safety is identified》.
Specimen size:100mm*100mm.
Test condition:Rate of pressure rise 20-100V/s
2. tensile strength and elongation at break
Method of testing reference standard GB/T 13542.2《Electric insulation film》.
Specimen size:200mm*15mm.
Draw speed:100mm/min.
3. interlaminar strength
Method of testing reference standard GB/T2790《180 ° of peeling strength test method flexible materials of adhesive are to rigid material
Material》.
Specimen size:200mm*15mm.
Draw speed:100mm/min.
4. backboard/EVA peel strengths
Method of testing reference standard GB/T2790《180 ° of peeling strength test method flexible materials of adhesive are to rigid material
Material》.
Specimen size:300mm*10mm.
Draw speed:100mm/min.
5. constant wet and heat ageing resistant performance
Method of testing reference standard GB/T2423.3《High-and-low temperature humid heat test method》.
Experimental condition:+ 85 DEG C, relative humidity 85%.
Test it is forward and backward to sample yellowness index (Δ YI) by GB GB 2409《Plastics yellow colour index test method》Determine.
6. water vapor transmittance
Method of testing reference standard ASTM F1249《Plastic foil is determined with modulated infrared sensor and thin plate water vapour is saturating
The test method of the property crossed》.
Experimental condition:+ 40 DEG C, relative humidity 100%.
Embodiment 1:
Backplane fabrication process is as follows:
First, by polyethylene terephthalate (du pont company) 85wt%, inorganic filler titanium dioxide R960 is (beautiful
E.I.Du Pont Company of state) 10wt%, hydrolysis stabilizer I powder (TUV chemistry) 3wt%, thermo oxidative aging agent four (3,5- bis-
Tertiary butyl-4-hydroxy) benzenpropanoic acid pentaerythritol ester (BASF Aktiengesellschaft) 2wt%, melt at 250-260 DEG C after being well mixed
After processing, after casting film-forming, biaxial tension is obtained 150 microns of thick intermediate layer films.
Then, in the weather-proof outer layer coating that 50 microns of a face roller coat in intermediate layer is thick.Outer layer coating dispensing is fluororesin
GK570 (Daikin) 70wt%, inorganic filler titanium dioxide R900 (du pont company) 20wt%, crosslinking agent hexa-methylene two
Isocyanate trimer (Bayer A.G) 4wt% and hexamethylene diisocyanate prepolymer (Bayer A.G)
5wt%, octoate catalyst stannous (Shanghai Xin Dian chemical materials Co., Ltd) 1wt%.Raw material is well mixed, it is solid at 150 DEG C
Change 3min to prepare.
Finally, in the improved polyalkene film that 500 microns of the another side showering in intermediate layer is thick.Wherein, improved polyalkene is thin
The dispensing of film is ethylene-butene copolymer (Dow Chemical company) 90wt%, and (win wound is special for modified additive hydroxy-ethyl acrylate
Kind of chemical company) 1wt% and silane grafted polyethylene (Ao Sijia companies of the U.S.) 7wt%, ultraviolet absorber 2- (2 '-hydroxyl-
3 '-tert-butyl group -5 '-aminomethyl phenyl) -5- chloro benzo triazole (BASF Aktiengesellschaft) 0.07wt%, light stabilizer 2,2,
6,6- tetramethyl -4- piperidines stearates (Taiwan double bond chemical company) 0.03wt%, four (3,5- bis- tertiary fourths of thermo oxidative aging agent
Base -4- hydroxyls) benzenpropanoic acid pentaerythritol ester (BASF Aktiengesellschaft) 0.1wt%, initiator 2,5- dimethyl -2, the double (benzene of 5-
Formyl peroxide)-hexane (Qingdao Rong Ji Chemical Co., Ltd.s) 1.8wt%.Raw material is well mixed, the thermosetting at a temperature of 130 DEG C
Change 5min to prepare.A kind of high pressure photovoltaic back S1 is obtained.
Embodiment 2:
Backplane fabrication process is as follows:
First, by polybutylene terephthalate (PBT) (du pont company) 80wt%, montmorillonite DK4 is (prosperous for inorganic filler
Brilliant science and technology) 15wt%, hydrolysis stabilizer UN-03 (the outstanding grace chemical industry in Shanghai) 4wt% ,-two (3- of thermo oxidative aging agent triethylene glycol ether
Tertiary butyl-4-hydroxy -5- aminomethyl phenyls) propionic ester (Taiwan forever Optical Chemical Company) 1wt%, at 250-260 DEG C after being well mixed
After melt-processed, after casting film-forming, biaxial tension is obtained 300 microns of thick intermediate layer films.
Then, in the weather-proof outer layer coating that 10 microns of a face roller coat in intermediate layer is thick.Outer layer coating dispensing is fluororesin
Lumiflon 200 (Japan AGC) 80wt%, inorganic filler titanium dioxide TR81 (Hensel Man of the U.S.) 10wt%, crosslinking
Agent isophorone diisocyanate trimer (Bayer A.G) 2wt% and many melamine methylol resin (cyclopentadienyls of mixed etherificate
Good chemical company) 7wt%, catalyst dibutyltin dilaurylate (Jinan multidimensional bridge chemical company) 0.2wt% and to toluene sulphur
Acid (Hangzhou chemical reagents corporation) 0.8wt%.Raw material is well mixed, is solidified 2min at 160 DEG C and is prepared.
Finally, in the improved polyalkene film that 100 microns of the another side showering in intermediate layer is thick.Wherein, improved polyalkene is thin
The dispensing of film be ethylene-octene copolymer (Dow Chemical company) 80wt%, modified additive 4- hydroxyl ester butyl methyl propylene
Acid esters (Ying Chuan Specialty Chemicals company) 5wt% and glycidyl methacrylate graft polyethylene (Nanjing Hua Dou scientific & technical corporation)
0.5wt%, inorganic filler titanium dioxide r902 (du pont company) 12wt%, ultraviolet absorber 2- hydroxyl -4- n-octyloxies two
Benzophenone (Taiwan forever Optical Chemical Company) 0.1wt%, light stabilizer are double (1- octyloxy -2,2,6,6- tetramethyl -4- piperidyls)
Sebacate (Taiwan forever Optical Chemical Company) 0.05wt%, thermo oxidative aging agent triethylene glycol ether-two (3- tertiary butyl-4-hydroxies-
5- aminomethyl phenyls) propionic ester (BASF Aktiengesellschaft) 0.05wt%, initiator 2,5- dimethyl -2, double (the benzoyl mistakes of 5-
Oxygen)-hexane (Qingdao Rong Ji chemical companies) 2.3wt%.Raw material is well mixed, at a temperature of 140 DEG C prepared by heat cure 2min
Obtain.A kind of high pressure photovoltaic back S2 is obtained.
Embodiment 3:
Backplane fabrication process is as follows:
First, by polyethylene naphthalate (Taiwan Changchun) 90wt%, inorganic filler titanium dioxide r902 (is shut out in the U.S.
Company of nation) 5wt%, hydrolysis stabilizer P400 (TUV chemistry) 3wt%, thermo oxidative aging agent 2'- di-2-ethylhexylphosphine oxides-(4- first
Base -6- tert-butyl phenols) (BASF Aktiengesellschaft) 2wt%, after being well mixed after 250-260 DEG C of melt-processed casting film-forming
Biaxial tension afterwards is obtained 250 microns of thick intermediate layer films.
Then, in the weather-proof outer layer coating that 20 microns of a face roller coat in intermediate layer is thick.Outer layer coating dispensing is fluororesin
41088 (Changxing chemistry) 90wt%, black (U.S.'s good fortune Lu) 5wt% of inorganic filler siderochrome, crosslinking agent hexamethylene diisocyanate
Prepolymer (Bayer A.G) 4.8wt%, catalyst monobutyltin oxide (traditional Chinese medicines Reagent Company) 0.2wt%.Raw material is mixed
Close uniform, solidify 3.5min at 155 DEG C and prepare.
Finally, in the improved polyalkene film that 200 microns of the another side showering in intermediate layer is thick.Wherein, improved polyalkene is thin
The dispensing of film be ethylene-propylene copolymer (Dow Chemical company) 75wt%, modified additive dimethylaminoethyl acrylate methyl base ammonia
Base ethyl ester (and wound chemical company) 8wt% and acrylamide graft polyethylene (Hua Lin chemical companies) 5wt%, inorganic filler calcining
Kaolin (BASF Aktiengesellschaft) 10wt%, ultraviolet absorber 2- (4,6- double (2,4- 3,5-dimethylphenyl) -1,3,5-triazines -
2- yls) -5- octyloxy phenol (BASF Aktiengesellschaft) 0.08wt%, light stabilizer poly-succinic (4- hydroxyl -2,2,6,6- tetramethyls
Base -1- piperidine ethanols) ester (BASF Aktiengesellschaft) 0.06wt%, thermo oxidative aging agent β-(3,5- di-t-butyl -4- hydroxy benzenes
Base) the positive octadecanol ester of propionic acid (Taiwan double bond chemical company) 0.04wt%, initiator normal-butyl 4, bis- (the tertiary fourths of peroxidating of 4-
Base) valerate (Qingdao Rong Ji Chemical Co., Ltd.s) 1.82wt%.Raw material is well mixed, the heat cure at a temperature of 135 DEG C
3.5min prepare.A kind of high pressure photovoltaic back S3 is obtained.
Embodiment 4:
Backplane fabrication process is as follows:
First, by polyethylene terephthalate (Taiwan Changchun) 95wt%, inorganic filler carbon black MA100 (Mitsubishis
Learn) 2wt%, hydrolysis stabilizer glycidyl neodecanoate (Dow Chemical company) 2.5wt%, thermo oxidative aging agent 1,3,
5- trimethyl -2,4,6- tri- (3,5- di-tert-butyl-4-hydroxyl benzyl) benzene (BASF Aktiengesellschaft) 0.5wt%, are well mixed
After 250-260 DEG C of melt-processed, after casting film-forming, biaxial tension is obtained 280 microns of thick intermediate layer films afterwards.
Then, in the weather-proof outer layer coating that 5 microns of a face roller coat in intermediate layer is thick.Outer layer coating dispensing is fluororesin 4102
(Changxing chemistry) 85wt%, inorganic filler carborundum (Jin Meng new materials company) 8wt%, many methylol trimerizations of crosslinking agent methyl-etherified
Melamine resin (Taiwan Changchun chemistry) 6wt%, catalyst phthalic acid (Hangzhou Sheng Li chemical companies) 1wt%.Raw material is mixed
Close uniform, solidify 3.5min at 145 DEG C and prepare.
Finally, in the improved polyalkene film that 200 microns of the another side showering in intermediate layer is thick.Wherein, improved polyalkene is thin
The dispensing of film be ethylene-vinyl acetate copolymer (Dow Chemical company) 95wt%, modified additive methacrylic acid two
Methylamino ethyl ester (BASF Aktiengesellschaft) 0.1wt% and silane grafted polyethylene (Ao Sijia companies of the U.S.) 0.1wt%,
Inorganic filler barium sulfate (Zhong Jiang chemical companies) 4wt%, ultraviolet absorber 3- [3- (2-H- BTA -2- bases) -4- hydroxyls -
5- tert-butyl-phenyls]-propionic acid-macrogol ester (Taiwan double bond chemical company) 0.1wt%, light stabilizer double (1,2,2,6,6-
Pentamethyl -4- piperidyls) (Taiwan is double for-sebacate/mono- (1,2,2,6,6- pentamethyl -4- piperidyls) sebacate compound
Key chemical company) 0.05wt%, thermo oxidative aging agent 3, double octadecane epoxide -2 of 9-, 4,8,10- tetra- oxygen -3,9- hosphospiros
[5.5] hendecane (Taiwan double bond chemical company) 0.05wt%, initiator are adjacent, and the o- tert-butyl group-o- (2- ethylhexyls)-mono--
Peroxycarbonates (Hai Jing chemical companies) 0.6wt%.Raw material is well mixed, at a temperature of 155 DEG C prepared by heat cure 3min
Obtain.A kind of high pressure photovoltaic back S4 is obtained.
Embodiment 5:
Backplane fabrication process is as follows:
First, will be poly- to naphthalenedicarboxylic acid butanediol ester (Taiwan Changchun) 87wt%, (Britain is beautiful for inorganic filler titanium dioxide R595
Li Lian companies) 8wt%, hydrolysis stabilizer P400 (TUV chemistry) 3.5wt%, thermo oxidative aging agent 9,10- dihydro-9-oxies
Miscellaneous -10- phospho hetero phenanthrenes -10- oxides (BASF AG) 1.5wt%, is cast after being well mixed after 250-260 DEG C of melt-processed
Biaxial tension after film forming is obtained 100 microns of thick intermediate layer films.
Then, in the weather-proof outer layer coating that 25 microns of a face roller coat in intermediate layer is thick.Outer layer coating dispensing is fluororesin T-1
(three love enrichments) 75wt%, inorganic filler titanium dioxide TR88 (Hensel Man of the U.S.) 17wt%, crosslinking agent isophorone two
Isocyanate prepolymer (Japanese polyurethane company) 7.9wt%, catalyst dibutyltin cinnamic acid dioctyl tin (the new allusion quotation chemical material in Shanghai
Co., Ltd) 0.1wt%.Raw material is well mixed, is solidified 5min at 140 DEG C and is prepared.
Finally, in the improved polyalkene film that 300 microns of the another side showering in intermediate layer is thick.Wherein, improved polyalkene is thin
The dispensing of film be ethylene-heptene copolymer (Dow Chemical company) 85wt%, modified additive ethoxy caprolactone methyl-prop
Olefin(e) acid (BASF Aktiengesellschaft) 1wt% and maleic anhydride grafted polyethylene (Hongyuan chemical company) 6wt%, inorganic filler titanium white
Powder R706 (du pont company) 6wt%, ultraviolet absorber 2- [4- [2- hydroxyl -3- dodecyloxy propyl group] epoxide] -2- hydroxyls
Base phenyl] double (2,4- 3,5-dimethylphenyl) -1,3,5-triazines (BASF Aktiengesellschaft) 0.08wt% of -4,6-, light stabilizer gathers
{ [6- [(1,1,3,3- tetramethyl butyls) amino]] -1,3,5- triazine -2,4- [(2,2,6,6,-tetramethyl-4-piperidyl) imido
(BASF Aktiengesellschaft) 0.04wt%, thermo oxidative aging agent phosphorous acid three (2,4- di-tert-butyl-phenyl) ester (German BASF
Company) 0.03wt%, initiator 3, double (t-butyl peroxy) ethyl butyrate (the rich Silin chemical company) 1.85wt% of 3-.By raw material
It is well mixed, at a temperature of 160 DEG C, heat cure 3.5min is prepared.A kind of high pressure photovoltaic back S5 is obtained.
Comparative example 1:
Photovoltaic back is buied on marketPYE SPV, structure is PET/PET/Primer, and thickness 295 ± 5 is micro-
Rice.
Performance detection is carried out to the material of a kind of high pressure backboard and comparative example 1 obtained in embodiment 1,2,3,4,5, as a result
As shown in table 1.
Table 1:The performance parameter of obtained high office's electric discharge pressure photovoltaic back
From data in table, crystal silicon component encapsulation of the present invention is used high pressure backboard, can meet the need of big system crystal silicon component
Ask.In addition, also having good reliability in terms of adhesive property, water vapor barrier property, mechanical strength, weatherability, can expire completely
Sufficient rear surface of solar cell protects the requirement as protective material.Preparation technology of the present invention is easy, and stable performance is not only greatly improved
The security of big system component, and important leverage is provided for component reduction supplementary material cost.
Claims (10)
1. high pressure backboard is used in a kind of crystal silicon component encapsulation, successively by base layer in the middle of modified olefin internal layer, polyester and crosslinking fluorine tree
The weather-proof outer layer composition of fat;Characterized in that, the modified olefin internal layer thickness is 100~1000 μm, it is 65% by mass fraction
~95% the first matrix resin, 0.1~10% modified additive A, 0.1~10% modified additive B, 0~30% it is inorganic
Filler, 0.001%~0.1% ultraviolet absorber, 0.001%~0.1% light stabilizer, 0.001%~0.1% heat resistanceheat resistant
Oxygen aging agent, 0.01%~5% initiator composition, first matrix resin is propylene, butylene, heptene, octene, norborneol
One or two monomers and ethene in alkene, vinylacetate, methyl acrylate form olefin-copolymerization according to any proportioning copolymerization
Thing;In the middle of the polyester matrix ligament thickness be 50~300 μm, by the second matrix resin that mass fraction is 80%~95%, 0~
15% inorganic filler, 0.1%~8% hydrolysis stabilizer, 0.01%~3% thermo oxidative aging agent be well mixed after
After 250-260 DEG C of melt-processed, Jing casting film-formings, biaxial tension are obtained;Second matrix resin is by poly terephthalic acid second
One kind or many in diol ester, polybutylene terephthalate (PBT), PEN, PBN
Plant and constitute according to any proportioning;The weather-proof outer layer thickness of fluororesin that is crosslinked is 5~50 μm, is 70%~90% by mass fraction
The 3rd matrix resin, 5%~20% inorganic filler, 1%~15% crosslinking agent, 0.001%~1% catalyst group
Into the 3rd matrix resin is fluororesin, by the poly- trifluoro-ethylene ether type fluorocarbon resin of hydroxyl, the poly- trifluoro-ethylene ester type fluorine of hydroxyl
One or more in carbon resin, hydroxyl polytetrafluoroethylene (PTFE) ether type fluorocarbon resin, hydroxyl polytetrafluoroethylene (PTFE) ester type fluorocarbon resin is pressed
Constitute according to any proportioning.
2. high pressure backboard according to claim 1, it is characterised in that the modified additive A is pressed for one or several following
According to the mixture of any proportioning composition:Acrylate, hydroxy-ethyl acrylate, hydroxypropyl acrylate, 4- hydroxyl ester butyl propyleneglycols
Acid esters, ethoxy caprolactone acrylic acid, acrylate, acrylic acid diethylamino ethyl ester, the tertiary fourth of acrylic acid
Base amino ethyl ester, urine base acrylate;The modified additive B is one or several following mixing constituted according to any proportioning
Thing:Silane grafted polyethylene, maleic anhydride grafted polyethylene, glycidyl methacrylate graft polyethylene, acrylamide
Grafted polyethylene.
3. high pressure backboard according to claim 1, it is characterised in that the inorganic filler be one or several following according to
The mixture that arbitrarily proportioning is constituted:Talcum powder, calcined kaolin, montmorillonite, mica powder, titanium dioxide, calcium carbonate, barium sulfate, silicon
Sour magnesium, aluminium hydroxide, magnesium hydroxide, carborundum, copper-chrome black, siderochrome are black, carbon black.
4. high pressure backboard according to claim 1, it is characterised in that the initiator is one or several following according to appointing
The mixture of meaning proportioning composition:Double (benzoyl the peroxide)-hexanes of benzoyl peroxide, 2,5- dimethyl -2,5-, the double (uncles of 3,3-
Butyl peroxy) ethyl butyrate, neighbour, o- tertiary pentyl-o- (2- ethylhexyls)-mono--peroxycarbonates, neighbour, the o- tert-butyl group-
O- isopropyl-mono--peroxycarbonates, neighbour, the o- tert-butyl group-o- (2- ethylhexyls)-mono--peroxycarbonates, normal-butyl
Double (the t-butyl peroxy)-hexanes of 4,4- bis- (tert-butyl peroxide) valerate, 2,5- dimethyl -2,5-.
5. high pressure backboard according to claim 1, it is characterised in that the ultraviolet absorber is pressed for one or several following
According to the mixture of any proportioning composition:ESCALOL 567, UV-531,2,4-
Dihydroxy benaophenonel, 2,2,4- trihydroxybenzophenones, 2- (2 '-hydroxyl -3 '-the tert-butyl group -5 '-aminomethyl phenyl) -5- chloros
BTA, 2- (2 '-hydroxyl -3 ', 5 '-di-t-butyl -5 '-aminomethyl phenyl) -5- chloro benzo triazoles, 3- [3- (2-H-
BTA -2- bases) -4- hydroxyl -5- tert-butyl-phenyls]-propionic acid-macrogol ester, 2- (2H- BTA -2- bases) -6- ten
Dialkyl group -4- methylphenols, 2- (2'- hydroxyl -5'- t-octyl phenyl) BTA, 2- (double (the 2,4- dimethyl benzenes of 4,6-
Base) -1,3,5- triazine -2- bases) -5- octyloxy phenol, 2- [4- [2- hydroxyl -3- tridecane epoxide propyl group] epoxide] -2- hydroxy benzenes
Base] -4,6- double (2,4- 3,5-dimethylphenyls) -1,3,5- triazines, 2- [4- [2- hydroxyl -3- dodecyloxy propyl group] epoxide] -2-
Hydroxy phenyl] double (2,4- the 3,5-dimethylphenyls) -1,3,5- triazines of -4,6-.
6. high pressure backboard according to claim 1, it is characterised in that the light stabilizer be one or several following according to
The mixture that arbitrarily proportioning is constituted:Double (1,2,2,6,6- pentamethyl -4- piperidyls)-sebacate/mono- (five first of 1,2,2,6,6-
Base -4- piperidyls) sebacate compound, bis(2,2,6,6-tetramethyl-4-piperidyl)sebacate, it is poly- [6- [(1,1,3,
3- tetramethyl butyls) amino]] -1,3,5- triazine -2,4- [(2,2,6,6,-tetramethyl-4-piperidyl) imido, it is double (1- octyloxies -
2,2,6,6- tetramethyl -4- piperidyls) sebacate, 2,2,6,6- tetramethyl -4- piperidines stearates, poly-succinic (4- hydroxyls
Base -2,2,6,6- tetramethyl -1- piperidine ethanols) ester.
7. high pressure backboard according to claim 1, it is characterised in that the thermo oxidative aging agent is one or several following
According to the mixture that any proportioning is constituted:Four (3,5- di-t-butyl -4- hydroxyls) benzenpropanoic acid pentaerythritol ester, β-(bis- uncles of 3,5-
Butyl -4- hydroxy phenyls) the positive octadecanol ester of propionic acid, 2'- di-2-ethylhexylphosphine oxides-(4- methyl-6-tert-butylphenols), 1,3,5- front threes
Base -2,4,6- three (3,5- di-tert-butyl-4-hydroxyl benzyls) benzene,-two (3- tertiary butyl-4-hydroxy -5- methylbenzenes of triethylene glycol ether
Base) propionic ester, 1,3,5- tri- (the 4- tert-butyl group -3- hydroxyl -2,6- dimethyl benzyls) -1,3,5- triazine -2,4,6- (1H, 3H,
5H)-triketone, phosphorous acid three (2,4- di-tert-butyl-phenyls) ester, double (2,4- di-tert-butyl-phenyls) pentaerythritol diphosphites,
Double four oxygen -3 of octadecane epoxide -2,4,8,10- of double (2,6- di-t-butyl -4- aminomethyl phenyls) pentaerythritol diphosphates, 3,9-,
The split isopropyl of the miscellaneous -10- phospho hetero phenanthrenes -10- oxides of 9- hosphospiros [5.5] hendecane, 9,10- dihydro-9-oxies, 4,4'- two
Phenyl C12-15- alcohol phosphite esters.
8. high pressure backboard according to claim 1, it is characterised in that the hydrolysis stabilizer is pressed for one or several following
According to the mixture of any proportioning composition:Monomer Carbodiimides hydrolysis stabilizer, polycarbodiimide class hydrolysis stabilizer, one
The glycidol hydrolysis of lipid stabilizer of first carboxylic acid.
9. high pressure backboard according to claim 1, it is characterised in that the crosslinking agent is one or several following according to appointing
The mixture of meaning proportioning composition:Hexamethylene diisocyanate trimer, hexamethylene diisocyanate prepolymer, different Fo Er
The many melamine methylol resins of ketone diisocyanate trimer, IPDI prepolymer, methyl-etherified, butyl ether
Many melamine methylol resins, many melamine methylol resins of mixed etherificate.
10. high pressure backboard according to claim 1, it is characterised in that the catalyst be one or several following according to
The mixture that arbitrarily proportioning is constituted:Stannous octoate, tin dilaurate dioctyl tin, monobutyltin oxide, three isooctyl acid tin of monobutyl,
Dibutyl tin laurate, acetic acid, p-methyl benzenesulfonic acid, phthalic acid, laurate, isooctyl acid.
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CN105609574A (en) * | 2015-12-28 | 2016-05-25 | 润峰电力有限公司 | High voltage ultralong anti-PID solar component |
CN106079773A (en) * | 2016-06-16 | 2016-11-09 | 杭州福斯特光伏材料股份有限公司 | A kind of power gain type solar energy back veneer material |
CN107629339B (en) * | 2017-10-25 | 2020-04-10 | 温州瑞阳光伏材料有限公司 | Grafted polyethylene crosslinked membrane and preparation method and application thereof |
CN111363394A (en) * | 2020-04-13 | 2020-07-03 | 常州回天新材料有限公司 | Transparent coating for solar photovoltaic cell module |
CN114231196A (en) * | 2020-09-07 | 2022-03-25 | 盐城百佳年代薄膜科技有限公司 | Impact-resistant EVA (ethylene-vinyl acetate copolymer) packaging adhesive film with three-layer structure, and preparation method and application thereof |
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CN104393084A (en) * | 2014-11-28 | 2015-03-04 | 明冠新材料股份有限公司 | Backboard for high heat dissipation photovoltaic module and preparation method |
CN104494263A (en) * | 2014-12-25 | 2015-04-08 | 杭州福斯特光伏材料股份有限公司 | High-partial-discharge-voltage photovoltaic backplane |
CN104512082A (en) * | 2014-11-27 | 2015-04-15 | 苏州赛伍应用技术有限公司 | Three-layer structural PET (polyethylene terephthalate) film and solar battery back plate prepared from three-layer structural PET film |
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CN104512082A (en) * | 2014-11-27 | 2015-04-15 | 苏州赛伍应用技术有限公司 | Three-layer structural PET (polyethylene terephthalate) film and solar battery back plate prepared from three-layer structural PET film |
CN104393084A (en) * | 2014-11-28 | 2015-03-04 | 明冠新材料股份有限公司 | Backboard for high heat dissipation photovoltaic module and preparation method |
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Address after: 311300 Ling'an Province, Hangzhou City, Jin Jin Bao street, North Street Patentee after: Hangzhou Forster applied materials Limited by Share Ltd Address before: 311300 Ling'an Province, Hangzhou City, Jin Jin Bao street, North Street Patentee before: Hangzhou First PV Material Co., Ltd. |