CN101317274A - Coating composition for solar cell protective covers - Google Patents
Coating composition for solar cell protective covers Download PDFInfo
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- CN101317274A CN101317274A CN 200680044840 CN200680044840A CN101317274A CN 101317274 A CN101317274 A CN 101317274A CN 200680044840 CN200680044840 CN 200680044840 CN 200680044840 A CN200680044840 A CN 200680044840A CN 101317274 A CN101317274 A CN 101317274A
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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 invention provides a solar cell protective cover which is not impaired in the transparency satisfactory for the protective cover for solar cells and has excellent room-temperature workability, solvent resistance, weather resistance and endurance; and a curable fluororesin coating composition capable of forming the cover. A curable fluororesin coating composition for solar cell protective covers comprising (A) a curable fluororesin, (B) a curing agent, and (C) a solvent, which is to be applied either directly to a transparent resin layer (II) formed on the side of a solar cell module (I) to be irradiated with sun rays or to a primer layer (IV) previously formed on the layer (II) and thus form a top coat layer (III) made of a cured fluororesin.
Description
Technical field
The present invention relates to a kind of protective cover and the curable fluorine-containing coating composition that is used to form this protective cover of solar cell; the transparency of the protective cover of described solar cell, solvent resistance, resistance to water (anti-poisture-penetrability), weatherability, durability, hardness of film, gloss excellence, and considered environmental protection.
Background technology
Now, the protective cover of solar cell uses glass plate.But glass is heavy and crisp, so proposed with lightweight and have the polycarbonate plate of the transparency, high index of refraction or the plate of transparent resin system such as the acrylic resin board base material of glass plate instead.But these transparent resins are wanting at weatherability, reagent resistance, anti-wound property, stain resistance etc., so still do not replace glass plate so far.
In addition, fluororesin has excellent weatherability, low-refraction, reagent resistance, water and oil-resistant, stain resistance based on the high-energy of intramolecular C-F key and hypopolarization rate, and it is applied to various uses.So,, then can improve weatherability, the transparency, reagent resistance, water and oil-resistant, stain resistance if can form fluororesin layer on transparent resin base material surface.
As the method that on the transparent resin base material, forms fluororesin layer, the method that attaches fluororesin film, the method for coating (application) coat composition of fluorine etc. are arranged usually, consider preferred rubbing method from simplicity, back processability, the aspect that can be used in complicated shape.
As the coat composition of fluorine that can be used in rubbing method, well-known have often be coated on the frying pan to give the coating composition that contains polytetrafluoroethylene (PTFE) of grease proofness, film in order to form, need be at high-temperature baking, so be not suitable for resin base material.
As can forming the fluororesin film, dissolve in organic solvent and film in the known copolymer that fluoroolefin and various hydro carbons monomers are arranged and be transparent normal temperature cure fluororesin in normal temperature cure.But fluororesin has excellent characteristics such as solvent resistance, can not only dissolve the strong solvent that fluororesin can also dissolve the ketone system or the ester system of other resins so have to use.
In Japanese kokai publication sho 57-34107 communique, as the curable coating composition with weatherability, the copolymer of fluoroolefin and alkyl vinyl ether and hydroxy alkyl vinethene is disclosed for example.In addition, in Japanese kokai publication sho 61-275311 communique, Japanese kokai publication sho 62-7767 communique, Japanese kokai publication hei 3-121107 communique and Japanese kokai publication hei 6-184243 communique, the curable fluororesin of using as curable coating with the copolymer of fluoroolefin, vinyl esters, alkyl vinyl ether and hydroxy alkyl vinethene is disclosed.In addition, Japanese kokai publication hei 6-271807 communique has proposed the good curable fluororesin of adaptation such as a kind of and Merlon.
But these fluorinated copolymers are dissolved in strong solvent, but are difficult to be dissolved in the weak Weak solvent of general solvent, particularly the third organic solvent resin dissolves energy such as (the third organic solvents of organic solvent poisoning prevention rules regulation).
In addition; in the time of will being used for the transparent resin base material based on the fluorine resin coating of strong solvent; resin base material also can dissolve; the transparency of transparent resin base material (light transmission) reduces greatly; so it is effectively as the common building materials that do not require heigh clarity with the internal part coating of coating and device, household electrical appliances, the protective cover use of the solar cell that still can't to consider its permeability as light be most important properties.
Expect that a kind of use do not dissolve the coat composition of fluorine of the Weak solvent of transparent resin matrix material, but the curable fluororesin that is dissolved in Weak solvent is very not known.
For example, as in the research of making aspect the solvent, put down in writing the non-curable fluororesin that dissolves in mineral essential oil (the third organic solvent) that constitutes by fluoroolefin and cyclohexyl vinethene in the Japanese kokai publication sho 53-96088 communique, and Japan has put down in writing the fluororesin that dissolves in the mineral essential oil of curable in the special fair 8-32847 communique.
But, though these fluororesin dissolve in general solvent, even but for the curable fluorine-containing copolymer in the special fair 8-32847 communique of Japan, the hydroxyl value of its introducing and the total amount of acid number are also in 30mgKOH/g, and in an embodiment, the hydroxyl value of the copolymer that the dissolubility in the mineral essential oil obtains confirming and acid number are all few to 5mgKOH/g, its curable is insufficient, so can not expect making moderate progress as aspects such as the solvent resistance of the favorable characteristics of fluororesin, weatherability, durability.
On the other hand; in field of solar cells; the use fluorine resin coating has been proposed as the protecting solar cell cover in the Japanese kokai publication sho 59-198773 communique; owing to be on solar module, directly to form to film; thereby as protective cover, fluororesin coating film has problems aspect intensity.
The fluororesin that has proposed to have fluorine-containing cycloaliphatic ring structure in the Japanese kokai publication hei 2-123771 communique is used for solar cell; but; be difficult to introduce cross-linking part for this fluororesin, so can not substantially improve as the desired solvent resistance of the protective cover of solar cell, weatherability, durability etc.
Summary of the invention
The protective cover and the curable fluorine-containing coating composition that can form this protective cover that the purpose of this invention is to provide a kind of solar cell; the transparency that it can not damage as the protective cover of solar cell has room temperature processability, solvent resistance, weatherability, durability.
Promptly; the present invention relates to the protective cover coating composition of solar cell; it is to contain (A) curable fluororesin, (B) curing agent and (C) the curable fluorine-containing coating composition of solvent; described composition is used to form directly or is arranged at the fluororesin solidfied material external coating (III) of transparent resin layer (II) across priming coat (IV), and described transparent resin layer (II) is arranged on the solar light irradiation face side of solar module (I).
In addition, the invention still further relates to the protective cover laminated film of solar cell and solar cell, described solar cell has solar module (I), transparent resin layer (II) and external coating (III), described transparent resin layer (II) is arranged on the solar light irradiation face side of this assembly (I), described external coating (III) directly or across priming coat (IV) is arranged at transparent resin layer (II), wherein, this external coating (III) is the solidfied material layer of above-mentioned protective cover with coating composition; The protective cover of described solar cell comprises transparent resin layer (II) and directly or be arranged at the external coating (III) of this transparent resin layer across priming coat (IV) with laminated film; it is the protective cover laminated film that is arranged at the solar light irradiation face side of solar module (I); wherein, this external coating (III) is the solidfied material layer of above-mentioned curable fluorine-containing coating composition.
Embodiment
The protective cover of solar cell of the present invention is used to form directly with coating composition or is arranged at the fluororesin solidfied material external coating (III) of transparent resin layer (II) across priming coat (IV), and described transparent resin layer (II) is arranged on the solar light irradiation face side of solar module (I).
The protective cover coating composition is to contain (A) curable fluororesin, (B) curing agent and (C) the curable fluorine-containing coating composition of solvent.
Below each composition is described.
(A) curable fluororesin
The curable fluororesin that uses among the present invention can only use the fluororesin with curable group, also can use the mixture of the non-fluororesin of the fluororesin of fluororesin with curable group and non-curable and/or curable or non-curable.In addition, can also be the mixture of the non-fluororesin of the fluororesin of non-curable and curable.
As the curable fluororesin, can enumerate following substances.
(A1) be dissolved in the curable fluororesin of Weak solvent, particularly the third organic solvent:
Can enumerate have the fluoroolefin unit, vinethene unit and have the copolymer of the monomeric unit of cure sites; Have fluoroolefin unit, vinyl ester units and have the copolymer etc. of the monomeric unit of cure sites.
As fluoroolefin, for example can enumerate tetrafluoroethene (TFE), hexafluoropropylene (HFP), chlorotrifluoroethylene (CTFE), perfluor (alkyl vinyl ether) (PAVE), trifluoro-ethylene (TrFE), vinylidene fluoride (VdF), ethylene fluoride etc.
As vinethene, can enumerate for example ethyl vinyl ether, cyclohexyl vinethene, ethylene methacrylic ether, normal-butyl vinethene, 2-ethylhexyl vinethene, isobutylvinyl ether, 2-methoxy ethyl vinethene etc.
As vinyl esters, can enumerate for example neodecanoic acid (versatic acid) vinyl esters (Veova 9 (trade name), the Veova 10 (trade name) etc. of shell chemistry society system), benzoic acid vinyl esters, vinyl acetate, vinyl propionate base ester, butyric acid vinyl esters, neopentanoic acid vinyl esters, caproic acid vinyl esters, p-tert-butyl benzoic acid vinyl esters etc.
For monomer, can enumerate for example hydroxy alkyl vinethenes such as hydroxybutyl vinethene (HBVE), hydroxypropyl vinethene as the monomer of hydroxyl with curable position; Hydroxy alkyl allyl ethers such as 2-hydroxyethyl allyl ether, 4-hydroxybutyl allyl ether; Hydroxy alkyl vinyl esters such as hydroxyethyl vinethene etc. can be enumerated for example acrylic acid, methacrylic acid, vinyl acetic acid, butenoic acid, undecenoic acid, maleic acid, maleic acid monoesters, maleic anhydride, fumaric acid, fumaric monoalkylester etc. as carboxylic construction unit.In addition, can also use vinyl silanes etc. contain silane monomer, contain epoxy radicals monomer, contain amino monomer etc.
As concrete example, can enumerate for example TFE/Veova 9/ benzoic acid vinyl esters/hydroxybutyl vinyl ether copolymers, CTFE/ ethyl vinyl ether/cyclohexyl vinethene/hydroxybutyl vinyl ether copolymers etc.
This curable fluororesin be hydroxyl value greater than the aggregate value of 5mgKOH/g and hydroxyl value and acid number greater than 30mgKOH/g contain the fluorinated copolymer of hydroxyl the time, the favorable solubility in Weak solvent, and solidification reactivity is also excellent is so be preferred.Hydroxyl value be 10mgKOH/g above, when above, be preferred in particular for 30mgKOH/g for improving solidification reactivity, hydroxyl value be 65mgKOH/g following, when following, be preferred in particular for 60mgKOH/g from the dissolubility aspect Weak solvent.
In addition, hydroxyl value is 5mgKOH/g when following, and curable reduces, and is in the inadequate trend that become such as solvent resistance, weatherability, durability, reagent resistance, hardness of film, adaptation.
Have under the situation of acid number, the total of also preferred hydroxyl value of curable fluororesin (A1) and acid number is greater than 30mgKOH/g.Adding up under the following situation of 30mgKOH/g of hydroxyl value and acid number, curable reduces, and is in the inadequate trend that become such as solvent resistance, weatherability, durability, reagent resistance, adaptation.
These curable fluororesin (A1) can also mix use with non-fluororesin such as acrylic resin, ammonia ester resins.This non-fluororesin can be a curable, also can be non-curable.
As acrylic resin, can enumerate in the past the acrylic resin as coating, for example (methyl) acrylic acid carbon number is the homopolymers of 1～10 Arrcostab or the copolymer of (methyl) acrylate that copolymer, side chain and/or main chain end have curable functional group etc.
(A2) contain the curable fluororesin (but except that above-mentioned (A1)) of tetrafluoroethene (TFE) and hydro carbons monomer:
Can enumerate have the TFE unit, hydro carbons monomeric unit, vinyl ester units and have the copolymer etc. of the monomeric unit of cure sites.
As vinyl esters and monomer, can enumerate above-mentioned example with cure sites.
As the hydro carbons monomer, can enumerate for example ethene, propylene, isobutene, butylene, amylene, hexene, heptene, octene etc.
As concrete example, can enumerate TFE/ isobutene/benzoic acid vinyl esters/hydroxybutyl vinyl ether copolymers, TFE/HFP/ ethene/benzoic acid vinyl esters/hydroxybutyl vinyl ether copolymers etc.
These curable fluororesin (A2) also can mix use with non-fluororesin such as acrylic resin, ammonia ester resins.This non-fluororesin can be a curable, also can be non-curable.
As acrylic resin, can enumerate above-mentioned example.
(A3) contain the curable fluororesin (but except that above-mentioned (A1)) of chlorotrifluoroethylene (CTFE):
Can enumerate the copolymer that has the CTFE unit, has the monomeric unit of cure sites, and also have copolymer of hydro carbons monomeric unit and/or vinethene unit etc. as required.
As the monomer with cure sites, vinethene and hydro carbons monomer, can enumerate above-mentioned example.
As concrete example, can enumerate CTFE/ ethyl vinyl ether/hydroxybutyl vinyl ether copolymers, CTFE/ ethene/ethyl vinyl ether/hydroxybutyl vinyl ether copolymers etc.
These curable fluororesin (A3) can also mix use with non-fluororesin such as acrylic resin, ammonia ester resins.This non-fluororesin can be a curable, also can be non-curable.
As acrylic resin, can enumerate above-mentioned example.
(A4) contain the curable fluororesin (but except that above-mentioned (A1)) of vinylidene fluoride (VdF):
The copolymer etc. that can enumerate the copolymer of the monomeric unit that has the VdF unit and have cure sites and also have hydro carbons monomeric unit, vinyl ester units and/or vinethene unit as required.
As the monomer with cure sites, vinethene, vinyl esters and hydro carbons monomer, can enumerate above-mentioned example.
These curable fluororesin (A4) can also mix use with non-fluororesin such as acrylic resin, ammonia ester resins.This non-fluororesin can be a curable, also can be non-curable.
As acrylic resin, can enumerate above-mentioned example.
(A5) contain the curable fluororesin of non-curable fluororesin and the non-fluororesin of curable:
As the fluororesin of non-curable, can use TFE based copolymer, CTFE based copolymer, VdF based copolymer etc.
As non-curable TFE resinoid, can enumerate for example TFE/ ethene/hexafluoropropylene copolymer etc.
As non-curable CTFE resinoid, can enumerate for example CTFE/ cyclohexyl vinyl ether copolymers etc.
As the VdF based copolymer of non-curable, can enumerate for example VdF/TFE/CTFE copolymer, VdF/TFE/HFP copolymer, VdF/HFP copolymer, VdF/CTFE copolymer etc.
As the non-fluororesin of curable, can enumerate curable acrylic resin, ammonia ester resin etc.
As the curable acrylic resin, can enumerate the curable acrylic resin that in the past was used for coating, preferred employing has the copolymer of (methyl) acrylate of curable functional group at side chain and/or main chain end.
Among these curable fluororesin (A), from using the solvent aspect of not infiltrating transparent resin and the transparency, aspect that reagent resistance is good, preferred consolidation fluororesin (A1), further, especially preferably contain the curable fluororesin (A1) of TFE as fluoroolefin from the good aspect of weatherability.
(B) curing agent
Curing agent selects best curing agent to get final product according to the kind of the curable group that the curable fluororesin has.
The curable group is under the situation of hydroxyl, and preferred isocyanate is that curing agent, amino resins are curing agent etc.
As the isocyanate-based curing agent, for example can enumerate 2, the 4-toluenediisocyanate, diphenyl-methane-4,4 '-vulcabond, XDI, IPDI, lysine methyl ester vulcabond, Methylcyclohexyl diisocyanate, trimethyl hexamethylene diisocyanate, hexamethylene diisocyanate, pentane-1, the 4-vulcabond, the tripolymer of above-mentioned substance, above-mentioned substance add adult or biuret body, the material that has the NCO more than 2 in the polymer of above-mentioned substance, and the isocyanates of blockization etc., but be not limited to these.
As amino resins is curing agent, can enumerate for example carbamide resin, melmac, benzoguanamine resin, glycoluril resin, in addition, can also enumerate the methylolation melmac of melamine through obtaining behind the methylolation, alkyl etherify melamine resin that the methylolation melamine obtains etc. after alcohols etherificates such as methyl alcohol, ethanol, butanols, but be not limited to these.
(C) solvent
As solvent,, consider preferred Weak solvent from the aspect that coatingization, dried coating film, various additive dissolubilities etc. are good so long as the solvent that does not infiltrate in the transparent resin that constitutes transparent resin layer (II) gets final product.
As Weak solvent, except for example the third organic solvent non-polar hydrocarbon organic solvents such as (coal tar naphtha of stipulating in the organic solvent poisoning prevention rules (Coal tar naphtha), mineral essential oil, turpentine oil, naphtha, benzinum, benzins), can also enumerate alcohol, glycol series solvent etc.Among these, from coatingization, dried coating film, the more excellent aspect of various additive dissolubilities, preferred non-polar hydrocarbon organic solvent, particularly as the third organic solvent of general solvent and coal tar naphtha, mineral essential oil.
In addition, consider the influence of transparent resin layer and coatingization, dried coating film, various additive dissolubility, base material adaptation etc., can use 1, in 4-dioxane, trichloroethylene, chloroform, aniline, pyridine, n-amyl alcohol, acetonitrile, butanone, acetone, butyl acetate, methyl acetate, dimethyl formamide, phenmethylol, ethanol, methyl alcohol, 1-butanols, diethylene glycol (DEG), monoethanolamine, ethylene glycol, formic acid, the water etc. one or more, and can together use with Weak solvent.
Mixed proportion in the curable fluorin resin composition of the present invention is as follows: with respect to 100 mass parts curable fluororesin (A), preferred 20～5000 mass parts, further preferred 60～1000 mass parts solvents (C) that add of adding, in equivalent proportion, add 0.5～1.5, further be 0.8～1.2 curing agent (B) with respect to the cure sites of curable fluororesin (A).
In the composition of the present invention, only otherwise the infringement transparency, adaptation, weatherability etc., the further various additives of interpolation.As additive, can enumerate for example surface hydrophilic agent, thermal resistance agent, ultra-violet absorber, coupling agent (silane system, metal system), antioxidant, pigment, filler, defoamer, thickener, levelling agent, curing accelerator, filler, anti-gelation agent etc.
The surface hydrophilic agent is to make film coated surface become the additive of hydrophilic surface, plays the effect that prevents that the rain stain from polluting.As preferred surface hydrophilic agent, for example can enumerate the international material that No. 96/26254 brochure etc. put down in writing that disclose, particularly from dividing a word with a hyphen at the end of a line property of surface, prevent the good aspect of rain stain contaminative, preferred following compound.
Acrylic esters of silicon acis shown in the formula (1) (acryl silicate) or fluorine-containing alkyl silicate or these oligomer:
[formula 1]
In the formula, n is 1～20 integer, R
1Complete different or at least 2 identical, all R
1All be that carbon number is 1～1000 1 valency organic group, and can contain oxygen atom, nitrogen-atoms and/or silicon atom, the part or all of hydrogen atom of this organic group can be replaced to fluorine atom or fluorine atom and chlorine atom.
Wherein, from dividing a word with a hyphen at the end of a line property of surface, prevent the good aspect of rain stain contaminative, more preferably R
1Part or all of hydrogen atom be replaced to fluorine atom.As concrete R
1, can enumerate F (CF
2)
n(CH
2)
m, (CF
3)
2CH, H (CF
2)
n(CH
2)
m, F (CF
2)
nCHFCF
2(CH
2)
m, F (CF
2)
n(CH
2)
mC=O, H (CF
2)
n(CH
2)
mC=O, (F (CF
2)
n(CH
2)
m)
2N, (H (CF
3)
2C)
2N, (H (CF
2)
n(CH
2)
m)
2N, F (CF
2)
nO (CF (CF
3) CF
2O)
mCF (CF
3) C=O (m is 0 or 1～6 integer, and n is 1～10 integer) etc.
With respect to the curable fluororesin (A) of 100 mass parts, its addition be preferably 0～100 mass parts, more preferably 0.1～50 mass parts, be preferably 1～20 mass parts especially.
The thermal resistance agent is by reflection, the infrared ray that the absorbs sunlight additive that the temperature of bottom (priming coat etc.) rises that prevents to film, and plays the effect that reduces internal temperature.As preferred thermal resistance agent, can enumerate the material that for example Japanese special fair 6-19061 communique, Japanese kokai publication hei 10-120946 communique, TOHKEMY 2000-72484 communique, TOHKEMY 2004-204173 communique etc. are put down in writing, particularly consider tin oxide (ATO), the indium oxide (ITO) of doped tin, the zinc oxide (AZO) of adulterated al, Ti oxide, the Ce oxide of preferred antimony dopant from the aspect of visible light permeability.
With respect to the curable fluororesin (A) of 100 mass parts, its addition be preferably 0～100 mass parts, more preferably 0.1～20 mass parts, be preferably 0.2～10 mass parts especially.
To cause film aging in order preventing to absorb the ultraviolet ray of sunlight, can to add ultra-violet absorber.As the concrete example of ultra-violet absorber, can enumerate benzophenone series, BTA system, triazine system, benzoic ether system, salicylate system, cyanoacrylate system, nickel complex system, oxanilide system etc.
Enumerate various commercially available products (trade name) below, but it is not limited to these, and can be used in combination.
The benzophenone series ultra-violet absorber:
Uvinul 3049, Uvinul 3050 (all being that BASF Amada Co., Ltd. makes); Sumisorb110, Sumisorb 130, Sumisorb 200 (being Sumitomo Chemical Company Ltd makes)
BTA is a ultra-violet absorber:
Tinuvin 900, Tinuvin PS, Tinuvin 384, Tinuvin 109, Tinuvin 928, Tinuvin 1130 (being Ciba Co., Ltd. makes); Sumisorb 250, Sumisorb 300, Sumisorb 320, Sumisorb 340, Sumisorb 350 (being Sumitomo Chemical Company Ltd makes); ADK STAB LA-32, ADK STAB LA-31 (being rising sun electrification Co., Ltd. makes)
Triazine is a ultra-violet absorber:
Tinuvin 400, Tinuvin 405, Tinuvin 479 (being Ciba Co., Ltd. makes)
Benzoic ether is a ultra-violet absorber:
Sumisorb 400 (Sumitomo Chemical Company Ltd's manufacturing)
Cyanoacrylate is a ultra-violet absorber:
Uvinul 3055, Uvinul 3039 (manufacturing of BASF Amada Co., Ltd.)
Other ultra-violet absorber:
Malonic acid [(4-methoxyphenyl)-methylene]-dimethyl ester
By suitable selection ultra-violet absorber,, also can suppress the xanthochromia phenomenon effectively even expose to the open air down long-standing.
From this angle, preferably begin to have BTA system, triazine system, the cyanoacrylate system of absorbability, and the excellent especially triazine of preferred ultraviolet absorption ability is a ultra-violet absorber from long wavelength side.
With respect to 100 mass parts curable fluororesin (A), its addition be preferably 0～50 mass parts, more preferably 0.5～10 mass parts, be preferably 1～5 mass parts especially.
Coupling agent has the effect of the adaptation of raising and transparent resin layer (base material).As silane is coupling agent, can enumerate and have for example epoxy radicals, amino, NCO, sulfydryl, (methyl) acrylate-based silane coupling agent, specifically can enumerate γ-glycidoxypropyltrime,hoxysilane, β-(3, the 4-epoxycyclohexyl) ethyl trimethoxy silane, γ-An Jibingjisanyiyangjiguiwan, γ-metacryloxy propyl trimethoxy silicane, γ-sulfydryl propyl-triethoxysilicane, OCNC
3H
6Si (OCH
3)
3Deng.As metal is coupling agent, for example can enumerating, aluminium is that coupling agent, titanium are coupling agent etc., specifically, can enumerate aluminium isopropoxide, aluminium ethylate, oacetic acid diisopropyl acid aluminium, three (oacetic acid) aluminium, alkyl acetoacetate diisopropyl acid aluminium, single acetyl pyruvic acid two (oacetic acid) aluminium, three (acetopyruvic acid) aluminium, ring-type aluminum isopropoxide, titanium chelate etc.
Among these, consider, preferably contain the silane coupling agent of epoxy radicals from coloring, adaptation aspect.
With respect to the curable fluororesin (A) of 100 mass parts, its addition be preferably 0～30 mass parts, more preferably 0.1～10 mass parts, be preferably 1～10 mass parts especially.
As antioxidant, can utilize various antioxidants.For example can enumerate hindered amine system, phenol system, phosphite ester system, vitamin E is antioxidant.
With respect to the curable fluororesin (A) of 100 mass parts, its addition is preferably 0～20 mass parts, more preferably 0.5～5 mass parts, be preferably 1～3 mass parts especially.
Curable fluorin resin composition of the present invention can be prepared by the common mixed methods such as mixing of mixer, roller mill.In addition, according to the kind of curable fluororesin, can be formed in and to be coated with preceding what is called 2 liquid type coating compositions curable fluororesin and curing agent mixing.
Described curable fluorin resin composition be coated on constitute the protecting solar cell cover transparent resin layer (base material) (II).
As constituting transparent resin layer (base material) transparent resin (II), preferably the light transmission rate of measuring with method described later is more than 80%, further is more than 85%, is in particular the resin more than 90%.
Specifically, can enumerate Merlon, PETG, acrylic resin, polyethylene, polypropylene, polystyrene, polyimides, epoxy resin etc.Among these, consider optimization polycarbonate, PETG, acrylic resin, polyimides, fluororesin, more preferably Merlon, acrylic resin, optimization polycarbonate especially from intensity, the good aspect of the transparency.
The transparency of Merlon is excellent, and mechanical properties such as hardness, versatility, processability aspect are also good, but known its marresistance, weatherability equal difference.In addition, consider from the thermal endurance aspect, when its be near the glass transition point temperature (150 ℃) the time can become soft, so it is unaccommodated need carrying out the resin of high-temperature baking, and the curable fluororesin that uses in the coating composition of the present invention is promptly curable at normal temperature, so be not topic to the Merlon application facet.
In addition, consider to form the such subbing layer of aftermentioned under adaptation, the impermeable situation of solvent at needs.
In addition, transparent resin layer (base material) can also be added on the various additives (but not comprising surface hydrophilic agent, the levelling agent that changes surface characteristic) that external coating (III) is mentioned when describing in (II).It is effective particularly adding thermal resistance agent, ultra-violet absorber, antioxidant etc.Its addition gets final product in above-mentioned scope.In addition, these additives can only add in the transparent resin layer (II), also can add to simultaneously in the external coating (III).The kind of the additive that is added can be identical with external coating (III), also can be different.
As the method that forms external coating (III) (being curable fluororesin solidfied material layer), can adopt (1) directly to be coated with and to make the method for its curing on (II) at transparent resin layer (base material); (2) priming coat (IV) is set at transparent resin layer (base material) on (II), on this priming coat (IV), is coated with and makes the method for its curing etc.
Directly in the rubbing method (1), the solvent (C) that uses in the curable fluorine-containing coating composition of the present invention need be for the solvent itself that do not infiltrate transparent resin layer (base material) transparent resin (II) or with the solvent that the do not infiltrate transparent resin mixed solvent as main solvent.This solvent that does not infiltrate transparent resin depends on the kind of transparent resin, but single solvent in the preferably above-mentioned Weak solvent or mixed solvent.For example, transparent resin is under the situation of Merlon, polyester, acrylic resin, is preferably one or more non-polar hydrocarbon kind solvent, particularly the third organic solvent.As blendable other solvents, can enumerate Weak solvent solvent described later in addition, its combined amount fixes on the amount of the transparency of not damaging transparent resin.
Form in the method (2) of external coating (III) across priming coat (IV), owing to can prevent the infiltration of solvent by priming coat (IV) to transparent resin, thereby can contain the solvent that infiltration may be arranged slightly to transparent resin, for example polar organic solvent in the curable fluorine-containing coating composition.
As subbing in this case, can use for example acrylic resin, ammonia ester resin, mylar, fluororesin etc.
In above-mentioned arbitrary method, as coating process, can adopt usual ways such as dipping, cast, roller coat, curtain coating, rod are coated with, spraying, spin coating, curing also can adopt methods such as air drying, baking drying, UV curing.Condition of cure is different because of the difference of solidifying system, but can adopt existing known condition.
The invention still further relates to solar cell; it is the solar cell with solar module (I), transparent resin layer (II) and external coating (III); described transparent resin layer (II) is arranged on the solar light irradiation face side of this assembly (I); described external coating (III) directly or across priming coat (IV) is arranged at transparent resin layer (II); wherein, this external coating (III) is the solidfied material layer of above-mentioned protective cover with coating composition.
In addition; the invention still further relates to the protective cover laminated film of solar cell; it comprises transparent resin layer (II) and directly or be arranged at the external coating (III) of this transparent resin layer across priming coat (IV); it is the protective cover laminated film that is arranged at the solar light irradiation face side of solar module (I); wherein, this external coating (III) is the solidfied material layer of above-mentioned curable fluorine-containing coating composition.
As solar module (I), be not particularly limited, can use the existing known assembly that solar cell (cell) is sealed to form with sealant or backboard etc.
Transparent resin layer (base material) (II) can form by directly coating solar cell; also can make the protective cover laminated film of the external coating (III) that lamination has the fluoro-containing coating solidfied material in advance; and this laminated film engaged with solar module (I), form transparent resin layer (base material) thus (II).
Transparent resin layer (base material) thickness (II) is preferably 50 μ m～15mm usually because of the difference of the kind of resin, the transparency etc. is different.
The thickness of external coating (III) is preferably 1 μ m～500 μ m usually because of the difference of the kind of curable fluororesin, the kind of transparent resin base material etc. is different.
Be provided with under the situation of priming coat (IV), the thickness of subbing layer is preferably 0.1 μ m～100 μ m usually because of the difference of the kind of subbing, the kind of transparent resin base material etc. is different.
Following mask body is enumerated preferred implementation of the present invention, but the invention is not restricted to these execution modes.
(execution mode 1)
(II) transparent resin:
Merlon
(III) external coating:
The solidfied material of following curable fluorine-containing coating composition
(A) curable fluororesin:
The curable fluororesin of above-mentioned (A1) (particularly TFE/ vinyl esters/contain the copolymer of the monomer of cure sites (hydroxyl or carboxyl))
(B) curing agent:
Isocyanate-based
(C) solvent:
The third organic solvent (particularly coal tar naphtha)
(D) additive:
Hydrophilic agent, ultra-violet absorber, silane coupling agent
(IV) priming coat:
Do not have
(execution mode 2)
(II) transparent resin: PETG
(III) external coating:
The solidfied material of following curable fluorine-containing coating composition
(A) curable fluororesin:
The curable fluororesin of above-mentioned (A1) (particularly CTFE/ vinethene/contain the copolymer of the monomer of cure sites (hydroxyl or carboxyl))
(B) curing agent:
Isocyanate-based
(C) solvent:
The third organic solvent (particularly mineral essential oil)
(D) additive:
Silane coupling agent, ultra-violet absorber
(IV) priming coat:
Do not have
(execution mode 3)
(II) transparent resin:
Acrylic resin
(III) external coating:
The solidfied material of following curable fluorine-containing coating composition
(A) curable fluororesin:
The curable fluororesin of above-mentioned (A1) (the particularly copolymer of the monomer of TFE/ vinyl esters/contain cure sites (hydroxyl or carboxyl) and the mixture of curable acrylic resin)
(B) curing agent:
Isocyanate-based
(C) solvent:
The third organic solvent (particularly coal tar naphtha)
(D) additive:
Ultra-violet absorber
(IV) priming coat:
Do not have
(execution mode 4)
(II) transparent resin:
Merlon
(III) external coating:
The solidfied material of following curable fluorine-containing coating composition
(A) curable fluororesin:
The curable fluororesin of above-mentioned (A2) (copolymer with TFE/ hydro carbons monomer/vinyl esters/contain the monomer of cure sites (hydroxyl or carboxyl) is the curable fluororesin that is dissolved in butyl acetate of representative)
(B) curing agent:
Isocyanate-based
(C) solvent:
Butyl acetate
(D) additive:
Ultra-violet absorber, hydrophilic agent
(IV) priming coat:
(non-curable acrylic resin) arranged
(execution mode 5)
(II) transparent resin:
Merlon
(III) external coating:
The solidfied material of following curable fluorine-containing coating composition
(A) curable fluororesin:
The curable fluororesin of above-mentioned (A2) (copolymer with TFE/ hydro carbons monomer/vinyl esters/contain the monomer of cure sites (hydroxyl or carboxyl) is the curable fluororesin that is dissolved in butyl acetate of representative)
(B) curing agent:
Isocyanate-based
(C) solvent:
Butyl acetate
(D) additive:
Ultra-violet absorber, hydrophilic agent
(IV) priming coat:
(UV curable acrylic resin) arranged
Coating composition of the present invention is suitable for the protective cover of solar cell most, when being applied to be in the article of the environment for use identical with the protective cover of solar cell, also can obtain the effect identical with the present invention.As these other article, can enumerate for example window, the daylighting portion of building, automobile, train, aircraft etc.; The roof in building, parking lot; The sound proof panel of road, windscreen; The lampshade of automobile, motorcycle etc.; Various illumination protective covers etc.
Embodiment
Next based on embodiment the present invention is described, but the present invention is not limited only to these embodiment.
The assay method that this specification uses is as follows.
(NMR analysis)
The NMR determinator: BRUKER society makes
1H-NMR condition determination: 300MHz (tetramethylsilane=0ppm)
19F-NMR condition determination: 282MHz (Arcton 11=0ppm)
(elementary analysis)
Determinator: the Ionalizer 901 that the CHN CORDER that J-SCIENCE Co., Ltd. makes and Orionresearch (オ リ オ リ サ one チ) Co., Ltd. make
(hydroxyl value and acid number)
The composition of obtaining according to NMR and elemental microanalysis method calculates.
(number-average molecular weight)
Determinator: the GPC (model HLC-8020) that TOSOH Co., Ltd makes
Condition determination: post uses 3 TSKgel:GMHXL, 1 G2500HXL, 1 GRCXL-L.As eluent, use oxolane, as the standard specimen of molecular weight, use the known polystyrene of molecular weight.
(glass transition temperature Tg)
According to ASTM E1356-98, DSC determinator 7 series of using Perkin Elmer to make in running for the second time, are determined Tg according to mid-point method.
Condition determination
Programming rate: 10 ℃/min
Sample size: 10mg
Heat cycle: 25 ℃～150 ℃, heat up, cool off, heat up
(dissolubility test)
" dissolve in organic solvent " and be meant and in the 100g organic solvent, can dissolve (solution is transparent) more than the 10g under 20 ± 5 ℃ the temperature.Be easy to the aspect consideration from preparation, the coating of coating composition, preferably in the 100g organic solvent, dissolve more than the 100g.
(mensuration of light transmission rate/haze value)
Use the smart mechanism of (strain) Japan to make the mist degree instrument II of manufacturing, measure based on ASTM D1003.
Production Example 1 (manufacturing of curable fluorine-containing copolymer)
In the stainless steel autoclave of capacity 6000ml, add 2500 mass parts butyl acetates, 554.5 mass parts Veova 9 (below be called " VV9 "), 69.1 mass parts vinyl benzoates (VBz), 83.5 mass parts 4-hydroxybutyl vinethenes (HBVE), after being cooled to 5 ℃, nitrogen replacement is carried out in decompression, repeats this operation 3 times.At last, decompression adds 280.0 mass parts tetrafluoroethene (TFE) once more.Stir down, be warmed up to 62.0 ℃, add 28.38 mass parts Perbutyl PV (trade name, the peroxidating system polymerization initiator that NOF Corp makes), initiated polymerization.Press in the reactor when 1.0MPaG is reduced to 0.4MPaG, stop reaction.The polymerization yield is 98.0%.Resulting fluorinated copolymer is used
19F-NMR,
1H-NMR and elemental microanalysis method are analyzed, and it is that TFE is that 37 moles of %, VV9 are that 45.2 moles of %, VBz are the fluorinated copolymer (1-1) that 7.0 moles of %, HBVE are 10.8 moles of % as can be known, and number-average molecular weight Mn is 9.0 * 1000.And glass transition temperature Tg is 30 ℃.Dissolubility in solvent (coal tar naphtha and mineral essential oil) is " solvable ".
In addition, except using the monomer shown in the table 1, similarly make the fluorinated copolymer (1-2) of hydroxyl.The composition of resulting copolymer, number-average molecular weight Mn, hydroxyl value and solvent (coal tar naphtha and mineral essential oil) dissolubility is listed in table 1.
Table 1
Embodiment 1
100 mass parts curable fluorine-containing copolymers (1-1) are dissolved in the 100 mass parts coal tar naphthas, obtain the solution that solid constituent is 50 quality %.In this solution of 200 mass parts, add 15.3 mass parts DURANATE TSA-100 (trade names, the isocyanate-based curing agent that Asahi Kasei Corporation makes), 4.0 mass parts Uvinul, 3039 (trade names, the ultra-violet absorber of BASF society system), 10.0 mass parts as the γ-glycidoxy propyl-triethoxysilicane of coupling agent and 50 mass parts as the coal tar naphtha that appends solvent, fully mix, make coating composition.
Embodiment 2
100 mass parts curable fluorine-containing copolymers (1-2) are dissolved in the 100 mass parts mineral essential oils, obtain the solution that solid constituent is 50 quality %.In this solution of 200 mass parts, add 12.4 mass parts DURANATE TSA-100,4.0 mass parts Uvinul, 3039,10.0 mass parts γ-glycidoxy propyl-triethoxysilicanes and and 50 mass parts as the mineral essential oil that appends solvent, fully mix, make coating composition.
Embodiment 3
100 mass parts curable fluorine-containing copolymers (1-1) are dissolved in the 100 mass parts coal tar naphthas, obtain the solution that solid constituent is 50 quality %.In this solution of 200 mass parts, add 15.3 mass parts DURANATE TSA-100,4.0 mass parts Uvinul, 3039,10.0 mass parts γ-glycidoxy propyl-triethoxysilicanes, 5 mass parts ZEFFLE GH700 (trade name, the hydrophilic agent that Daikin Ind Ltd makes; Fluorine-containing alkyl silicate) and 50 mass parts as appending the coal tar naphtha of solvent, fully mix, make coating composition.
Embodiment 4
(methyl methacrylate/cyclohexyl methacrylate/2-EHA/2-hydroxyethyl methacrylate copolymer is dissolved in the 100 mass parts coal tar naphthas, makes the clear solution that solid constituent is 50 quality % with 50 mass parts curable fluorine-containing copolymers (1-1) and 50 mass parts acrylic resins.
In this solution of 200 mass parts, add 15.3 mass parts DURANATE TSA-100,4.0 mass parts Uvinul, 3039,5 mass parts ZEFFLE GH700 and 50 mass parts as the coal tar naphtha that appends solvent, fully mix, make coating composition.
Embodiment 5
100 mass parts curable fluorine-containing copolymers (1-1) are dissolved in the 100 mass parts coal tar naphthas, obtain the solution that solid constituent is 50 quality %.In this solution of 200 mass parts, add 15.3 mass parts DURANATE TSA-100,4.0 mass parts Uvinul, 3039,5.0 mass parts ZEFFLEGH700 and 50 mass parts as the coal tar naphtha that appends solvent, fully mix, make coating composition.
Embodiment 6
At 200 mass parts TFE is curable fluororesin solution (the ZEFFLE GK510 (trade name) that Daikin Ind Ltd makes, solid constituent: 50 quality %, solvent: butyl acetate, hydroxyl value 60mgKOH/g, acid number 9mgKOH/g; Curable fluorine-containing copolymer 1-3) adds 21.0 mass parts Sumijoule N3300 (trade names in, the isocyanate-based curing agent that Zhuhua Bayer Aminoacyl Esterase Co., Ltd makes), 4.0 mass parts Uvinul 3039 and 50 mass parts are as the butyl acetate that appends solvent, fully mix, make coating composition.
Embodiment 7
At 154 mass parts TFE is curable fluororesin solution (the ZEFFLE GK570 (trade name) that Daikin Ind Ltd makes, solid constituent: 65 quality %, solvent: butyl acetate, hydroxyl value 60mgKOH/g, acid number 3mgKOH/g; Curable fluorine-containing copolymer 1-4) adds 20.6 mass parts Sumijoule N3300,4.0 mass parts Uvinul, 3039,5.0 mass parts ZEFFLE GH700 and 96 mass parts in as the butyl acetate that appends solvent, fully mix, make coating composition.
Embodiment 8
With 60 mass parts VdF is non-curable fluororesin (the ZEFFLE LC700 (trade name) that Daikin Ind Ltd makes, VdF/TFE/CTFE copolymer; Curable fluorine-containing copolymer 1-5) and 40 mass parts acrylic resins (methyl methacrylate/cyclohexyl methacrylate/2-EHA/2-hydroxyethyl methacrylate) copolymer be dissolved in the 100 mass parts coal tar naphthas, make the clear solution that solid constituent is 50 quality %.
In this solution of 100 mass parts, add 5.8 mass parts Sumijoule N3300,4.0 mass parts Uvinul, 3039,5.0 mass parts ZEFFLE GH700, fully mix, make coating composition.
Embodiment 9～12 and comparative example 1
After the surperficial degreasing with polycarbonate membrane (the Iupilon film FE-2000 (trade name) that Mitsubishi engineering Plastics Co., Ltd makes, thickness 100 μ m), to the coating composition of preparation among its difference air-atomizing embodiment 1～5, being coated with into dry film thickness is 50 μ m.Then,, make its dry solidification, make the protective cover laminated film 80 ℃ of heating 20 minutes.
For the protective cover laminated film of made, light transmittance, haze value and outward appearance before the development test; Light transmittance after the accelerated weathering test, haze value and outward appearance; Light transmittance after the humidity test and haze value; And adaptation, actual exposed contaminative, solvent resistance.The results are shown in table 2.In the table 2, comparative example 1 is the polycarbonate membrane with external coating of the present invention.
(outward appearance)
Visual valuation.
(accelerated weathering test)
Use super UV test machine W13 type (trade name, the atmospheric exposure test machine that Iwasaki Electric Co., Ltd. makes), carry out quickening in 200 hours weather resistance test.Experimental condition is as follows: shine 11 hours (illumination: 100mW/cm
2, blackboard temperature: 70%), 11 hours (illumination: 0mW/cm of dewfall 63 ℃, relative humidity:
2, blackboard temperature: 100%), the 1 hour (illumination: 0mW/cm of stopping room temperature, relative humidity:
2, blackboard temperature: 63 ℃, relative humidity: 85%).
(humidity test)
In the Constant Temperature and Humidity Chambers LH-20-01La ((strain) Nagano science machinery production institute) that breadboard is hung from above in 80 ℃ of atmosphere temperatures, humidity 85%, carry out test in 1000 hours, before and after test, measure light transmission rate, haze value.
(adaptation)
Carry out the test of chessboard grid based on JIS K5400.
(actual exposed contaminative)
Roof in 4 layers of house of industrial area, Osaka is installed in breadboard on the exposure platform of southern horizontal tilt 30 degree, carries out exposure test.Expose 1 month, the brightness (L of the aberration of determination test plate
*Value), with poor (the Δ L before and after the test
*) estimate.
(solvent resistance)
Based on following standard, visual valuation is with the state of the film coated surface of the cotton that contains butyl acetate after to the friction 100 times of filming.
A: no abnormal.
B: what have some crows.
C: the dissolving of filming, perhaps swelling has and significantly sends out crow.
Embodiment 13
With the acrylic panel (acrylic panel that Japan Test Panel Co., Ltd. makes; thickness 1mm) replace polycarbonate membrane as the transparent resin base material, the composition that uses embodiment 5 is as coating composition, in addition; form external coating similarly to Example 9, make the protective cover laminated film.
For the protective cover laminated film of making, study physical property similarly to Example 9.The results are shown in table 2.
Table 2
Embodiment 14～16 and comparative example 2
With polycarbonate membrane (the Iupilon film FE-2000 (trade name) that Mitsubishi engineering Plastics Co., Ltd makes, thickness 100 μ m) after the surperficial degreasing, with rod coater (peace Tian Jingji Co., Ltd. makes) #18 acrylic resins of painting is that (20 mass fraction average molecular weights are 40,000 to subbing, Tg=45 ℃, acid number is the solution of methyl methacrylate/ethyl acrylate/methacrylic acid copolymer in the mixed solvent of 56 mass parts isopropyl alcohols and 24 mass parts n-propyl acetates of 12mgKOH/g), making dry film thickness is 5 μ m, 80 ℃ of heating 20 minutes, form priming coat.
The coating composition of preparation among the difference air-atomizing embodiment 6～8 on this priming coat, being coated with into dry film thickness is 50 μ m.Then,, make its dry solidification, make the protective cover laminated film 80 ℃ of heating 20 minutes.
For the protective cover laminated film of making, study physical property similarly to Example 9.The results are shown in table 3.In the table 3, comparative example 2 is not for being provided with priming coat directly is coated with the coating composition formation of embodiment 6 at polycarbonate membrane laminated film.
Table 3
Embodiment 17
At 154 mass parts TFE is curable fluororesin solution (the ZEFFLE GK570 (trade name) that Daikin Ind Ltd makes; Curable fluorine-containing copolymer 1-4) adds 20.6 mass parts Sumijoule N3300,2.0 mass parts Tinuvin 479 (triazine that Ciba Co., Ltd. makes is a ultra-violet absorber), 2.0 mass parts Tinuvin 400 (triazine that Ciba Co., Ltd. makes is a ultra-violet absorber) and 96 mass parts in as the butyl acetate that appends solvent, fully mix, make coating composition.
Embodiment 18
At 154 mass parts TFE is curable fluororesin solution (the ZEFFLE GK570 (trade name) that Daikin Ind Ltd makes; Curable fluorine-containing copolymer 1-4) adds 20.6 mass parts Sumijoule N3300,2.0 mass parts Tinuvin 479,2.0 mass parts Tinuvin, 400,5.0 mass parts ZEFFLE GH700 and 96 mass parts in as the butyl acetate that appends solvent, fully mix, make coating composition.
Embodiment 19～20
With polycarbonate membrane (the Iupilon film FE-2000 (trade name) that Mitsubishi engineering Plastics Co., Ltd makes, thickness 100 μ m) after the surperficial degreasing, with rod coater (peace Tian Jingji Co., Ltd. makes) #18 acrylic resins of painting is that (20 mass fraction average molecular weights are 40,000 to subbing, Tg=45 ℃, acid number is the solution of methyl methacrylate/ethyl acrylate/methacrylic acid copolymer in the mixed solvent of 56 mass parts isopropyl alcohols and 24 mass parts n-propyl acetates of 12mgKOH/g), making dry film thickness is 5 μ m, 80 ℃ of heating 20 minutes, form priming coat.
The coating composition of preparation among the difference air-atomizing embodiment 17～18 on this priming coat, being coated with into dry film thickness is 50 μ m.Then,, make its dry solidification, make the protective cover laminated film 80 ℃ of heating 20 minutes.
For the protective cover laminated film of making, study physical property similarly to Example 9.Further carry out 500 hours accelerated weathering test, study the variation of its outward appearance.The results are shown in table 4.
Table 4
Utilizability on the industry
According to the present invention, can provide without detriment to as the transparency of the protective cover of solar cell and Have room temperature processability, solvent resistance, weatherability, durability solar cell protective cover and Can form the curable fluorine-containing coating composition of this protective cover.
Claims (10)
1, a kind of protective cover coating composition of solar cell; it is for containing (A) curable fluororesin, (B) curing agent and (C) the curable fluorine-containing coating composition of solvent; described composition is used to form directly or is arranged at the fluororesin solidfied material external coating (III) of transparent resin layer (II) across priming coat (IV), and described transparent resin layer (II) is arranged on the solar light irradiation face side of solar module (I).
2, protective cover coating composition as claimed in claim 1, wherein, described curable fluororesin (A) is the curable fluororesin (A1) that dissolves in the third organic solvent.
3, protective cover coating composition as claimed in claim 2, wherein, described curable fluororesin (A1) is the fluorinated copolymer of hydroxyl, its hydroxyl value is greater than 5mgKOH/g, and the aggregate value of hydroxyl value and acid number is greater than 30mgKOH/g.
4, as each described protective cover coating composition in the claim 1～3, wherein, described solvent (C) is a non-polar hydrocarbon class organic solvent.
5, as each described protective cover coating composition in the claim 1～4, wherein, described curing agent (B) is that isocyanate-based curing agent or amino resins are curing agent.
6, as each described protective cover coating composition in the claim 1～5, wherein, described fluororesin solidfied material external coating (III) directly is arranged at transparent resin layer (II).
7, as each described protective cover coating composition in the claim 1～6, wherein, the light transmittance of described transparent resin layer (II) is more than 80%.
8, as each described protective cover coating composition in the claim 1～7, wherein, described transparent resin layer (II) is layer of polycarbonate, PETG layer or acrylate resin layer.
9, a kind of solar cell; it comprises solar module (I), be arranged on the transparent resin layer (II) and directly or be arranged at the external coating (III) of this transparent resin layer across priming coat (IV) of the solar light irradiation face side of this assembly; wherein, this external coating (III) is the solidfied material layer that each described protective cover is used coating composition in the claim 1～8.
10, a kind of protective cover laminated film of solar cell; it is the protective cover laminated film that is arranged at the solar light irradiation face side of solar module (I); described laminated film comprises transparent resin layer (II) and directly or be arranged at the external coating (III) of this transparent resin layer across priming coat (IV); wherein, this external coating (III) is the solidfied material layer of each described curable fluorine-containing coating composition in the claim 1～8.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP346730/2005 | 2005-11-30 | ||
| JP2005346730 | 2005-11-30 | ||
| JP078179/2006 | 2006-03-22 |
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN201110436056.8A Division CN102544149B (en) | 2005-11-30 | 2006-11-14 | The protective cover laminated film of solaode and solaode |
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| CN101317274A true CN101317274A (en) | 2008-12-03 |
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN 200680044840 Pending CN101317274A (en) | 2005-11-30 | 2006-11-14 | Coating composition for solar cell protective covers |
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| CN (1) | CN101317274A (en) |
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