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WO2019128962A1 - 一种太阳能电池用封装胶膜及其制备方法和应用 - Google Patents

一种太阳能电池用封装胶膜及其制备方法和应用 Download PDF

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Publication number
WO2019128962A1
WO2019128962A1 PCT/CN2018/123373 CN2018123373W WO2019128962A1 WO 2019128962 A1 WO2019128962 A1 WO 2019128962A1 CN 2018123373 W CN2018123373 W CN 2018123373W WO 2019128962 A1 WO2019128962 A1 WO 2019128962A1
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Prior art keywords
resin
solar cell
film
film layer
cell according
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Ceased
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PCT/CN2018/123373
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English (en)
French (fr)
Inventor
王磊
郑亚
陈洪野
宇野敬一
吴小平
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Cybrid Technologies Inc
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Cybrid Technologies Inc
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Priority to US16/958,138 priority Critical patent/US12269973B2/en
Priority to EP18897412.5A priority patent/EP3733804B1/en
Publication of WO2019128962A1 publication Critical patent/WO2019128962A1/zh
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

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    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J7/00—Adhesives in the form of films or foils
    • C09J7/30—Adhesives in the form of films or foils characterised by the adhesive composition
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J7/00—Adhesives in the form of films or foils
    • C09J7/10—Adhesives in the form of films or foils without carriers
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J11/00—Features of adhesives not provided for in group C09J9/00, e.g. additives
    • C09J11/02—Non-macromolecular additives
    • C09J11/04—Non-macromolecular additives inorganic
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J11/00—Features of adhesives not provided for in group C09J9/00, e.g. additives
    • C09J11/02—Non-macromolecular additives
    • C09J11/06—Non-macromolecular additives organic
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J4/00—Adhesives based on organic non-macromolecular compounds having at least one polymerisable carbon-to-carbon unsaturated bond ; adhesives, based on monomers of macromolecular compounds of groups C09J183/00 - C09J183/16
    • C09J4/06—Organic non-macromolecular compounds having at least one polymerisable carbon-to-carbon unsaturated bond in combination with a macromolecular compound other than an unsaturated polymer of groups C09J159/00 - C09J187/00
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00—Use of inorganic substances as compounding ingredients
    • C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
    • C08K3/20—Oxides; Hydroxides
    • C08K3/22—Oxides; Hydroxides of metals
    • C08K2003/2227—Oxides; Hydroxides of metals of aluminium
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00—Use of inorganic substances as compounding ingredients
    • C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
    • C08K3/20—Oxides; Hydroxides
    • C08K3/22—Oxides; Hydroxides of metals
    • C08K2003/2237—Oxides; Hydroxides of metals of titanium
    • C08K2003/2241—Titanium dioxide
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00—Use of inorganic substances as compounding ingredients
    • C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
    • C08K3/24—Acids; Salts thereof
    • C08K3/26—Carbonates; Bicarbonates
    • C08K2003/265—Calcium, strontium or barium carbonate
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00—Use of inorganic substances as compounding ingredients
    • C08K3/01—Use of inorganic substances as compounding ingredients characterized by their specific function
    • C08K3/013—Fillers, pigments or reinforcing additives
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00—Use of inorganic substances as compounding ingredients
    • C08K3/34—Silicon-containing compounds
    • C08K3/36—Silica
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J2203/00—Applications of adhesives in processes or use of adhesives in the form of films or foils
    • C09J2203/322—Applications of adhesives in processes or use of adhesives in the form of films or foils for the production of solar panels
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J2203/00—Applications of adhesives in processes or use of adhesives in the form of films or foils
    • C09J2203/33—Applications of adhesives in processes or use of adhesives in the form of films or foils for batteries or fuel cells
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J2301/00—Additional features of adhesives in the form of films or foils
    • C09J2301/10—Additional features of adhesives in the form of films or foils characterized by the structural features of the adhesive tape or sheet
    • C09J2301/12—Additional features of adhesives in the form of films or foils characterized by the structural features of the adhesive tape or sheet by the arrangement of layers
    • C09J2301/122—Additional features of adhesives in the form of films or foils characterized by the structural features of the adhesive tape or sheet by the arrangement of layers the adhesive layer being present only on one side of the carrier, e.g. single-sided adhesive tape
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J2301/00—Additional features of adhesives in the form of films or foils
    • C09J2301/20—Additional features of adhesives in the form of films or foils characterized by the structural features of the adhesive itself
    • C09J2301/208—Additional features of adhesives in the form of films or foils characterized by the structural features of the adhesive itself the adhesive layer being constituted by at least two or more adjacent or superposed adhesive layers, e.g. multilayer adhesive
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J2301/00—Additional features of adhesives in the form of films or foils
    • C09J2301/40—Additional features of adhesives in the form of films or foils characterized by the presence of essential components
    • C09J2301/408—Additional features of adhesives in the form of films or foils characterized by the presence of essential components additives as essential feature of the adhesive layer
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J2301/00—Additional features of adhesives in the form of films or foils
    • C09J2301/40—Additional features of adhesives in the form of films or foils characterized by the presence of essential components
    • C09J2301/414—Additional features of adhesives in the form of films or foils characterized by the presence of essential components presence of a copolymer
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J2423/00—Presence of polyolefin
    • C09J2423/04—Presence of homo or copolymers of ethene
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J2429/00—Presence of polyvinyl alcohol
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J2431/00—Presence of polyvinyl acetate
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J2471/00—Presence of polyether
    • H—ELECTRICITY
    • H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10F—INORGANIC SEMICONDUCTOR DEVICES SENSITIVE TO INFRARED RADIATION, LIGHT, ELECTROMAGNETIC RADIATION OF SHORTER WAVELENGTH OR CORPUSCULAR RADIATION
    • H10F19/00—Integrated devices, or assemblies of multiple devices, comprising at least one photovoltaic cell covered by group H10F10/00, e.g. photovoltaic modules
    • H10F19/80—Encapsulations or containers for integrated devices, or assemblies of multiple devices, having photovoltaic cells
    • H10F19/804—Materials of encapsulations
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E10/00—Energy generation through renewable energy sources
    • Y02E10/50—Photovoltaic [PV] energy

Definitions

  • the invention relates to a packaging film for a solar cell and a preparation method and application thereof.
  • the white film can be used in the lower layer of the module to improve the power of the component by reflecting visible light and near-infrared light. It can be applied to single glass components and double glass components. The appearance requirements of the components are relatively demanding, and it is required that the white film cannot overflow to the battery sheets, the bus bars, the solder ribbons, and there are no defects such as wrinkles.
  • Pre-crosslinking process The pre-crosslinking makes the film partially cross-linked, thereby achieving the purpose of controlling white overflow. Disadvantages: poor peeling force, the components are not heat-resistant.
  • low-melting finger process reduce the possibility of white overflow by reducing the resin melt finger.
  • Disadvantages The ability to control overflow is not the best, the components still have flanges.
  • non-woven composite process through the composite of a layer of non-woven fabric, so as to achieve the purpose of controlling white overflow.
  • Disadvantages foreign matter (non-woven fabric) is introduced into the module, and long-term reliability is poor.
  • the technical problem to be solved by the present invention is to provide a packaging film for a solar cell which can solve the white overflow problem well, and a preparation method and application thereof.
  • the present invention adopts the following technical solutions:
  • An object of the present invention is to provide a package film for a solar cell, comprising a transparent layer in contact with the cell sheet, and a first film layer in contact with the transparent layer,
  • the raw material of the first film layer comprises the following components: a resin having a mass ratio of 3 to 25:1 and a colored filler, and a cross-linking of 0.1% to 5% of the total mass of the resin and the colored filler.
  • a co-crosslinking agent which comprises 0.1% to 1% of the total mass of the resin and the colored filler, and 0.1% to 1% of the total mass of the resin and the colored filler.
  • the resin and the colored filler have a total mass of 0.1% to 1% of a light stabilizer, and 0.1% to 5% of the total mass of the resin and the colored filler.
  • the mass ratio of the resin and the colored filler in the first film layer is 3 to 5:1.
  • the encapsulating film for a solar cell further comprises a second film layer in contact with the back sheet or the glass.
  • the encapsulating film for a solar cell further comprises one or more third adhesive film layers disposed between the first adhesive film layer and the second adhesive film layer.
  • the first adhesive film layer, the second adhesive film layer, and the transparent layer are not limited to one layer, and may be a plurality of layers of the same formulation.
  • the third film layer may be a film layer of a conventional formulation.
  • the raw material of the second film layer comprises a resin having a mass ratio of 15 to 25:1 and a colored filler.
  • the raw material of the second film layer further comprises 0.1% to 5% of a total amount of the crosslinking agent of the resin and the colored filler, the resin and the colored a co-crosslinking agent having a total mass of the filler of 0.1% to 1%, a coupling agent comprising 0.1% to 1% of the total mass of the resin and the colored filler, and a total mass of the resin and the colored filler 0.1% to 1% light stabilizer.
  • the second adhesive film layer in the present invention is also a white layer, but the amount of the white filler added is small relative to the first adhesive film layer. Therefore, the second adhesive film layer can well maintain the adhesion to the back sheet or the glass.
  • the connection performance at the same time, the total thickness of the second film layer and the first film layer is large, the reflectivity is high, and the power is increased.
  • the transparent layer has a thickness of 20 to 60 microns. If the thickness of the transparent layer is too thick, although the white overflow can be better prevented, it will affect the power of the solar cell; if the transparent layer is too thin, the ability to prevent white overflow is limited.
  • the physical properties of the film are not significantly changed by the addition of the titanium dioxide or the presence of the pre-crosslinked layer due to the presence of the transparent layer, and there is no significant change in peeling force, surface hardness, and the like of the cell sheet.
  • the raw material of the transparent layer comprises the following components: a resin, a crosslinking agent in an amount of 0.1% to 5% by mass of the resin, and a co-crosslinking agent in an amount of 0.1% to 1% by mass of the resin.
  • the coupling agent accounts for 0.1% to 1% by mass of the resin
  • the light stabilizer accounts for 0.1% to 1% by mass of the resin.
  • the resin is one or more selected from the group consisting of EVA, POE, and PVB.
  • the resin in the first adhesive film layer, the second adhesive film layer and the transparent layer may be the same resin or different resins.
  • the colored filler is one or more selected from the group consisting of titanium dioxide, calcium carbonate, silicon dioxide, aluminum oxide, and zinc titanium white.
  • the colored filler in the first adhesive film layer and the second adhesive film layer may be the same colored filler or different colored fillers.
  • the colored filler in the present invention is a white filler.
  • the photoinitiator is selected from the group consisting of 2-hydroxy-2-methyl-1-phenyl-1-propanone, 1-hydroxycyclohexyl phenyl ketone, benzophenone, (2, 4, 6-trimethylbenzoyl)diphenylphosphine oxide, 2-benzyl-2-dimethylamino-1-(4-morpholinylphenyl)butanone, 2-hydroxy-1-(4-( One or more of 2-hydroxy-2-methylpropionylphenyl)benzyl)-2-methyl-1-propanone, a macromolecular photoinitiator thioxanthone, and a visible light initiator camphor .
  • the crosslinking agent is selected from the group consisting of a crosslinking agent, tert-butyl 2-ethylhexyl carbonate, t-butyl peroxy-isopropyl carbonate, dibenzoyl peroxide, and dioxygen peroxide.
  • the crosslinking agents in the first adhesive film layer, the second adhesive film layer, and the transparent layer may be the same or different.
  • the co-crosslinking agent is selected from the group consisting of trimethylolpropane triacrylate, 2-trimethylolpropane tetraacrylate, ethoxylated trimethylolpropane triacrylate, ethoxylated trimethylol
  • propane triacrylate and trimethylolpropane triacrylate are selected from the group consisting of propane triacrylate and trimethylolpropane triacrylate.
  • the co-crosslinking agents in the first adhesive film layer, the second adhesive film layer, and the transparent layer may be the same or different.
  • the coupling agent is selected from the group consisting of 3-methacryloxypropylmethyltrimethoxysilane, 3-glycidylpropyltrimethoxysilane, vinyltrimethoxysilane, 3-ammonia One or more of propyltriethoxysilane and vinyltrimethoxysilane.
  • the coupling agents in the first film layer, the second film layer, and the transparent layer may be the same or different.
  • the light stabilizer is selected from the group consisting of bis(2,2,6,6-tetramethyl-4-piperidyl)sebacate, polysuccinic acid (4-hydroxy-2,2, 6,6-Tetramethyl-1-piperidineethanol), poly- ⁇ [6-[(1,1,3,3-tetramethylbutyl)-imino]-1,3,5-three Pyrazin-2,4-diyl][2-(2,2,6,6-tetramethylpiperidinyl)-azyl]-ylidene-[4-(2,2,6,6-tetra One or more of methylpiperidinyl)-amino.
  • the light stabilizers in the first film layer, the second film layer, and the transparent layer may be the same or different.
  • Another object of the present invention is to provide a method for preparing the package film for a solar cell, comprising the following steps:
  • Step (1) after preparing the first adhesive film layer and the raw material of the transparent layer separately, casting the film through an extruder;
  • Step (2) on the side of the transparent layer, irradiating with UV light to pass UV through the transparent layer to the first adhesive film layer and causing a cross-linking reaction on the surface of the first adhesive film layer;
  • the packaged film for solar cells is obtained by drawing and winding after cooling.
  • step (1) uses a co-extrusion casting machine for casting film formation.
  • the processing temperature of step (1) is from 60 to 110 °C.
  • the winding is cooled by a three-roller setting.
  • the cooling temperature in the step (3) is 20 to 50 °C.
  • a third object of the present invention is to provide an application of the above-described encapsulant film for a solar cell in a solar cell.
  • the present invention has the following advantages compared with the prior art:
  • the invention adopts a transparent layer and a first adhesive film layer, wherein a layer in contact with the battery sheet is a transparent layer, and the transparent layer blocks the white matter in the first adhesive film layer from overflowing to the battery sheet and the confluence to a certain extent.
  • the strip and the strip have a certain degree of prevention of white overflow; the photoinitiator is added to the formulation of the first film layer, and during the preparation process, the UV light penetrates the transparent layer to reach the first film layer.
  • the surface of the first film layer is caused to crosslink, so that the surface of the first film layer has a pre-crosslinked layer, and the presence of the pre-crosslinked layer further effectively prevents white overflow.
  • the encapsulating film of the invention has good adhesion to the cell sheet and the glass or the back sheet, has high reflectivity, and has a large power increase for the solar cell.
  • Figure 1 is a schematic view showing the structure of the present invention
  • 1 is a transparent layer
  • 2 is a first adhesive film layer
  • 3 is a second adhesive film layer.
  • the transparent layer 1 has a thickness of 50 ⁇ m and its raw material composition is: EVA: 100 kg; 2-ethylhexyl carbonate t-butyl ester: 0.6 kg, triallyl isocyanate: 0.8 kg, trimethylolpropane triacrylate Ester: 0.6 kg, 3-methacryloxypropylmethyltrimethoxysilane: 0.5 kg, bis(2,2,6,6-tetramethyl-4-piperidyl)sebacate: 0.2kg.
  • the first film layer 2 has a thickness of 300 ⁇ m, and its raw material composition is: EVA: 82 kg; titanium white powder: 18 kg, tert-butyl 2-ethylhexyl carbonate: 0.5 kg, 2-hydroxy-2-methyl -1-Phenyl-1-propanone: 1.2 kg, triallyl isocyanate: 0.7 kg, trimethylolpropane triacrylate: 0.5 kg, 3-methacryloxypropylmethyltrimethoxysilane : 0.4 kg, bis(2,2,6,6-tetramethyl-4-piperidyl) sebacate: 0.3 kg.
  • EVA 82 kg
  • titanium white powder 18 kg
  • tert-butyl 2-ethylhexyl carbonate 0.5 kg
  • 2-hydroxy-2-methyl -1-Phenyl-1-propanone 1.2 kg
  • triallyl isocyanate 0.7 kg
  • trimethylolpropane triacrylate 0.5 kg
  • the second film layer 3 has a thickness of 50 ⁇ m, and its raw material components are: EVA: 94 kg; titanium white powder: 6 kg; 2-ethylhexyl carbonate t-butyl ester: 0.8 kg, triallyl isocyanate: 0.9 kg , Trimethylolpropane triacrylate: 0.4kg, 3-methacryloxypropylmethyltrimethoxysilane: 0.5kg, bis(2,2,6,6-tetramethyl-4-piperidin Pyridyl) sebacate: 0.6 kg.
  • the preparation method is:
  • Step (1) mixing the raw materials of the first adhesive film layer 2, the second adhesive film layer 3 and the transparent layer 1 separately, and then plasticizing by a co-extrusion casting machine and extruding into a film through a T-shaped die.
  • Processing temperature is set to 80 ° C;
  • Step (2) after exiting the die, on the side of the transparent layer 1, the UV light is irradiated through the transparent layer 1 to reach the first adhesive film layer 2, and the product is in a molten state and has a high temperature because the die is just out of the die.
  • the photoinitiator on the surface of the first film layer 2 is caused to generate free radicals, and the radicals further induce cross-linking reaction on the surface of the first film layer 2 to form a pre-crosslinked layer;
  • step (3) the product treated by the step (2) is shaped by a three-roller, and then cooled at 20 ° C to be drawn up to obtain a packaging film for a solar cell.
  • Embodiment 1 It is basically the same as Embodiment 1, except that the resin in the first film layer, the second film layer, and the transparent layer is POE.
  • Example 2 It is basically the same as Example 2 except that the photoinitiator in the second film layer is 1-hydroxycyclohexyl phenyl ketone.
  • Example 2 It is basically the same as Example 2 except that the photoinitiator in the second film layer is benzophenone.
  • Example 2 It is basically the same as Example 2 except that the photoinitiator in the second film layer is 2-hydroxy-1-(4-(2-hydroxy-2-methylpropionylphenyl)benzyl)- 2-methyl-1-propanone.
  • Example 2 Basically the same as Example 2 except that the photoinitiator in the second film layer was 2-benzyl-2-dimethylamino-1-(4-morpholinylphenyl)butanone.
  • Example 2 Basically the same as Example 1, except that the thickness of the transparent layer was 60 ⁇ m.
  • Example 2 Basically the same as Example 1, except that the thickness of the transparent layer was 40 ⁇ m.
  • Example 2 Basically the same as Example 1, except that the thickness of the transparent layer was 20 ⁇ m.
  • Example 2 It is basically the same as Example 1, except that the EVA of the raw material of the first film layer is 75 kg; the titanium white powder is 25 kg.
  • Example 2 It is basically the same as Example 1, except that the EVA of the raw material of the first film layer is 83 kg; the titanium white powder is 17 kg.
  • Example 2 The same as Example 1 except that the photoinitiator in the raw material of the first film layer was added in an amount of 2 kg.
  • Example 2 It is basically the same as Example 1, except that the photoinitiator in the raw material of the first film layer is added in an amount of 3 kg.
  • Example 2 It is basically the same as Example 1, except that the photoinitiator in the raw material of the first film layer is added in an amount of 5 kg.
  • Example 2 The same as Example 1 except that the photoinitiator in the raw material of the first film layer was added in an amount of 0.5 kg.
  • Example 2 It is basically the same as Example 1, except that the EVA in the second film layer is 94 kg; the titanium dioxide: 6 kg.
  • Example 2 It is basically the same as Example 1, except that the EVA in the second film layer is 96 kg; the titanium white powder: 4 kg.
  • the first film layer has a thickness of 350 ⁇ m and does not contain a second film layer.
  • Embodiment 2 It is basically the same as Embodiment 1, except that a layer of a conventional third white film layer of 50 ⁇ m thick is further disposed between the first film layer and the second film layer.
  • Example 2 It is basically the same as Example 1, except that EVA in the first film layer: 90 kg; titanium dioxide: 10 kg.
  • Example 2 Basically the same as Example 1, except that the thickness of the transparent layer was 70 ⁇ m.
  • Example 2 Basically the same as Example 1, except that the thickness of the transparent layer was 10 ⁇ m.
  • the method for testing the degree of crosslinking, peeling force and reflectance in the present invention refers to GB/T29848-2013 (national standard "ethylene-vinyl acetate copolymer (EVA) film for photovoltaic module packaging").
  • the test method of component power refers to the IEC61215 standard.

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Abstract

本发明涉及一种太阳能电池用封装胶膜，包括与电池片相接触的透明层、与所述的透明层相接触的第一胶膜层，所述的第一胶膜层的原料包括如下组分：质量比为3～25:1的树脂和有色填料、占所述的树脂和所述的有色填料总质量0.1％～5％的交联剂、占所述的树脂和所述的有色填料总质量0.1％～1％的助交联剂、占所述的树脂和所述的有色填料总质量0.1％～1％的偶联剂、占所述的树脂和所述的有色填料总质量0.1％～1％的光稳定剂、占所述的树脂和所述的有色填料总质量0.1％～5％的光引发剂。本发明能有效地防止白色上溢。

Description

一种太阳能电池用封装胶膜及其制备方法和应用 技术领域
本发明涉及一种太阳能电池用封装胶膜及其制备方法和应用。
背景技术
白色胶膜可以用在组件下层，通过反射可见光及近红外光达到提高组件功率的目的，可以应用在单玻组件及双玻组件上。对组件外观要求比较苛刻，要求白色胶膜不能上溢至电池片、汇流条、焊带上，同时不能有褶皱等缺陷。
现有技术中通常采用如下方案来解决白色胶膜的白色上溢问题：
1、预交联工艺：通过预交联使得胶膜部分交联，从而达到控制白色上溢的目的。缺点：剥离力差，组件不耐热烘。
2、低熔指工艺：通过降低树脂熔指来降低白色上溢的可能性。缺点：控制上溢的能力不算最好，组件仍有翻边。
3、无纺布复合工艺：通过复合一层无纺布，从而达到控制白色上溢的目的。缺点：组件中引入异物(无纺布)，长期可靠性差。
发明内容
本发明所要解决的技术问题是提供一种能够很好的解决白色上溢问题的太阳能电池用封装胶膜及其制备方法和应用。
为解决以上技术问题，本发明采取如下技术方案：
本发明的一个目的是提供一种太阳能电池用封装胶膜，包括与电池片相接触的透明层、与所述的透明层相接触的第一胶膜层，
所述的第一胶膜层的原料包括如下组分：质量比为3～25:1的树脂和有色填料、占所述的树脂和所述的有色填料总质量0.1％～5％的交联剂、占所述的树脂和所述的有色填料总质量0.1％～1％的助交联剂、占所述的树脂和所述的有色填料总质量0.1％～1％的偶联剂、占所述的树脂和所述的有色填料总质量0.1％～1％的光稳定剂、占所述的树脂和所述的有色填料总质量0.1％～5％的光引发剂。
优选地，所述的第一胶膜层中所述的树脂和所述的有色填料的质量比为3～5:1。
优选地，所述的太阳能电池用封装胶膜还包括与所述的背板或玻璃相接触的第二胶膜层。
进一步优选地，所述的太阳能电池用封装胶膜还包括设置在所述的第一胶膜层和所述的第二胶膜层之间的一层或几层第三胶膜层。
本发明中，第一胶膜层、第二胶膜层和透明层并非限定为一层，可以是相同配方的多层。第三胶膜层可以是采用常规配方的胶膜层。
进一步优选地，所述的第二胶膜层的原料包括质量比为15～25:1的树脂和有色填料。
更为优选地，所述的第二胶膜层的原料还包括占所述的树脂和所述的有色填料总质量0.1％～5％的交联剂、占所述的树脂和所述的有色填料总质量0.1％～1％的助交联剂、占所述的树脂和所述的有色填料总质量0.1％～1％的偶联剂、占所述的树脂和所述的有色填料总质量0.1％～1％的光稳定剂。
本发明中的第二胶膜层也为白色层，但相对第一胶膜层来说，白色填料的添加量少，因此，第二胶膜层可以很好的维持与背板或玻璃的粘接性能，同时，第二胶膜层和第一胶膜层的总厚度大，反射率高，功率提升大。
优选地，所述的透明层的厚度为20～60微米。若透明层的厚度太厚，虽然能够更好的阻止白色上溢，但是会影响太阳能电池的功率；若透明层太薄，则阻止白色上溢的能力有限。
本发明中，由于透明层的存在，使得胶膜物性并没有因为钛白粉的添加或者预交联层的存在而明显改变，与电池片的剥离力、表面硬度等都没有明显改变。
优选地，所述的透明层的原料包括如下组分：树脂、占所述的树脂质量0.1％～5％的交联剂、占所述的树脂质量0.1％～1％的助交联剂、占所述的树脂质量0.1％～1％的偶联剂、占所述的树脂质量0.1％～1％的光稳定剂。
优选地，所述的树脂为选自EVA、POE、PVB中的一种或几种。
本发明中，第一胶膜层、第二胶膜层和透明层中的树脂可以为 相同的树脂，也可以为不同的树脂。
优选地，所述的有色填料为选自钛白粉、碳酸钙、二氧化硅、三氧化二铝、锌钛白中的一种或几种。
本发明中，第一胶膜层、第二胶膜层中的有色填料可以为相同的有色填料，也可以为不同的有色填料。
进一步优选地，本发明中的有色填料为白色填料。
优选地，所述的光引发剂为选自2-羟基-2-甲基-1-苯基-1-丙酮、1-羟基环己基苯基甲酮、二苯甲酮、(2,4,6-三甲基苯甲酰基)二苯基氧化膦、2-苄基-2-二甲基氨基-1-(4-吗啉苯基)丁酮、2-羟基-1-(4-(2-羟基-2-甲基丙酰基苯基)苄基)-2-甲基-1-丙酮、大分子光引发剂硫杂蒽酮类、以及可见光引发剂樟脑琨中的一种或几种。
优选地，所述的交联剂为选自交联剂过氧化2-乙基己基碳酸叔丁酯、叔丁基过氧化-异丙基碳酸酯、过氧化二苯甲酰、过氧化二异丙苯、2,5-二甲基-2,5-双(叔丁基过氧基)己烷、过氧化环己酮、叔丁基过氧化氢、过氧苯甲酸叔丁酯、过氧乙酸叔丁酯、过氧重碳酸二-(4-叔丁基环己基)酯、叔丁基过氧化-3,5,5-三甲基己酸酯、三烯丙基异氰酸酯中的一种或几种。
本发明中，第一胶膜层、第二胶膜层和透明层中的交联剂可以相同也可以不同。
优选地，所述的助交联剂为选自三羟甲基丙烷三丙烯酸酯、2-三羟甲基丙烷四丙烯酸酯、乙氧化三羟甲基丙烷三丙烯酸酯、乙氧化三羟甲基丙烷三丙烯酸酯、丙氧化三羟甲基丙烷三丙烯酸酯中的一种或几种。
本发明中，第一胶膜层、第二胶膜层和透明层中的助交联剂可以相同也可以不同。
优选地，所述的偶联剂为选自3-甲基丙烯酰氧基丙基甲基三甲氧基硅烷、3-缩水甘油丙基三甲氧基硅烷、乙烯基三甲氧基硅烷、3-氨丙基三乙氧基硅烷、乙烯基三甲氧基硅烷中的一种或几种。
本发明中，第一胶膜层、第二胶膜层和透明层中的偶联剂可以相同也可以不同。
优选地，所述的光稳定剂为选自双(2,2,6,6-四甲基-4-哌啶基)癸二酸酯、聚丁二酸(4-羟基-2,2,6，6-四甲基-1-哌啶乙醇)酯、聚-{[6-[(1,1,3,3-四甲基丁基)-亚氨基]-1,3,5-三嗪-2，4-二基][2-(2,2,6,6-四甲基哌啶基)-氮基]-亚已基-[4-(2,2,6,6-四甲基哌啶基)-氨基]中的一种或几种。
本发明中，第一胶膜层、第二胶膜层和透明层中的光稳定剂可以相同也可以不同。
本发明的另一个目的是提供一种所述的太阳能电池用封装胶膜的制备方法，包括依次进行的如下步骤：
步骤(1)、将所述的第一胶膜层和所述的透明层的原料分别配制好后，通过挤出机流延成膜；
步骤(2)、在所述的透明层所在侧，通过UV灯照射使得UV穿过透明层到达所述的第一胶膜层并促使所述的第一胶膜层的表面发生交联反应；
步骤(3)、冷却后牵引收卷制得所述的太阳能电池用封装胶膜。
优选地，步骤(1)采用共挤流延机进行流延成膜。
优选地，步骤(1)的加工温度为60～110℃。
优选地，步骤(3)中，通过三辊定型后冷却收卷。
优选地，步骤(3)中的冷却温度为20～50℃。
本发明的第三个目的是提供一种所述的太阳能电池用封装胶膜在太阳能电池中的应用。
由于以上技术方案的实施，本发明与现有技术相比具有如下优点：
本发明通过采用透明层和第一胶膜层，其中，与电池片接触的一层为透明层，透明层在一定程度上阻隔了第一胶膜层中的白色物质上溢到电池片、汇流条、焊带上，起到了一定程度的防止白色上溢的目的；第一胶膜层的配方中增加了光引发剂，在制备过程中，UV光穿透透明层，到达第一胶膜层并引发第一胶膜层表面物质进行交联反应，使得第一胶膜层的表面有一层预交联层，这层预交联层的存在，进一步有效地防止白色上溢。
本发明的封装胶膜与电池片和玻璃或背板的粘结力好，反射率 高，对太阳能电池的功率提升大。
附图说明
附图1为本发明的结构示意图；
其中，1为透明层；2为第一胶膜层；3为第二胶膜层。
具体实施方式
下面结合具体实施例对本发明做进一步详细的说明，但本发明并不限于以下实施例。实施例中采用的实施条件可以根据具体使用的不同要求做进一步调整，未注明的实施条件为本行业中的常规条件。本领域普通技术人员在没有做出创造性劳动前提下所获得的所有其它实施例，都属于本发明保护的范围。
实施例1
透明层1的厚度为50微米，其原料组分为：EVA：100kg；过氧化2-乙基己基碳酸叔丁酯：0.6kg、三烯丙基异氰酸酯：0.8kg、三羟甲基丙烷三丙烯酸酯：0.6kg、3-甲基丙烯酰氧基丙基甲基三甲氧基硅烷:0.5kg、双(2,2,6,6-四甲基-4-哌啶基)癸二酸酯：0.2kg。
第一胶膜层2的厚度为300微米，其原料组分为：EVA：82kg；钛白粉：18kg，过氧化2-乙基己基碳酸叔丁酯：0.5kg、2-羟基-2-甲基-1-苯基-1-丙酮:1.2kg、三烯丙基异氰酸酯：0.7kg、三羟甲基丙烷三丙烯酸酯：0.5kg、3-甲基丙烯酰氧基丙基甲基三甲氧基硅烷:0.4kg、双(2,2,6,6-四甲基-4-哌啶基)癸二酸酯：0.3kg。
第二胶膜层3的厚度为50微米，其原料组分为：EVA：94kg；钛白粉：6kg；过氧化2-乙基己基碳酸叔丁酯：0.8kg、三烯丙基异氰酸酯：0.9kg、三羟甲基丙烷三丙烯酸酯：0.4kg、3-甲基丙烯酰氧基丙基甲基三甲氧基硅烷：0.5kg、双(2,2,6,6-四甲基-4-哌啶基)癸二酸酯：0.6kg。
制备方法为：
步骤(1)、将第一胶膜层2、第二胶膜层3和透明层1的原料分别混合均匀，然后经共挤流延机塑化并经T形模具挤出流延成膜，加工温度设定为80℃；
步骤(2)、出模头后，在透明层1所在侧，通过UV灯照射使 得UV穿过透明层1到达第一胶膜层2，由于刚出模头，产品处于熔融状态，温度较高，经过UV灯照射后，促使第一胶膜层2表面的光引发剂产生自由基，自由基进一步引发第一胶膜层2的表面发生交联反应生成一层预交联层；
步骤(3)、经过步骤(2)处理的产品通过三辊定型，然后在20℃冷却后牵引收卷制得太阳能电池用封装胶膜。
实施例2
与实施例1基本相同，不同之处在于：第一胶膜层、第二胶膜层、透明层中的树脂均采用POE。
实施例3
与实施例2基本相同，不同之处在于：第二胶膜层中的光引发剂为1-羟基环己基苯基甲酮。
实施例4
与实施例2基本相同，不同之处在于：第二胶膜层中的光引发剂为二苯甲酮。
实施例5
与实施例2基本相同，不同之处在于：第二胶膜层中的光引发剂为2-羟基-1-(4-(2-羟基-2-甲基丙酰基苯基)苄基)-2-甲基-1-丙酮。
实施例6
与实施例2基本相同，不同之处在于：第二胶膜层中的光引发剂为2-苄基-2-二甲基氨基-1-(4-吗啉苯基)丁酮。
实施例7
与实施例1基本相同，不同之处在于：透明层的厚度为60微米。
实施例8
与实施例1基本相同，不同之处在于：透明层的厚度为40微米。
实施例9
与实施例1基本相同，不同之处在于：透明层的厚度为20微米。
实施例10
与实施例1基本相同，不同之处在于：第一胶膜层的原料中的EVA为75kg；钛白粉为25kg。
实施例11
与实施例1基本相同，不同之处在于：第一胶膜层的原料中的EVA为83kg；钛白粉为17kg。
实施例12
与实施例1基本相同，不同之处在于：第一胶膜层的原料中的光引发剂的添加量为2kg。
实施例13
与实施例1基本相同，不同之处在于：第一胶膜层的原料中的光引发剂的添加量为3kg。
实施例14
与实施例1基本相同，不同之处在于：第一胶膜层的原料中的光引发剂的添加量为5kg。
实施例15
与实施例1基本相同，不同之处在于：第一胶膜层的原料中的 光引发剂的添加量为0.5kg。
实施例16
与实施例1基本相同，不同之处在于：第二胶膜层中的EVA为94kg；钛白粉：6kg。
实施例17
与实施例1基本相同，不同之处在于：第二胶膜层中的EVA为96kg；钛白粉：4kg。
实施例18
与实施例1基本相同，不同之处在于：第一胶膜层的厚度为350微米，不含有第二胶膜层。
实施例19
与实施例1基本相同，不同之处在于：第一胶膜层和第二胶膜层之间还设置有一层50微米厚的常规的第三白色胶膜层。
实施例20
与实施例1基本相同，不同之处在于：第一胶膜层中的EVA：90kg；钛白粉：10kg。
对比例1
与实施例1基本相同，不同之处在于：透明层的厚度为70微米。
对比例2
与实施例1基本相同，不同之处在于：透明层的厚度为10微米。
各实施例和对比例的实验数据参见表1。
本发明中交联度、剥离力、反射率测试方法参照GB/T29848-2013(国标《光伏组件封装用乙烯-醋酸乙烯酯共聚物(EVA)胶膜》)。组件功率的测试方法参照IEC61215标准。
表1
Figure PCTCN2018123373-appb-000001
Figure PCTCN2018123373-appb-000002
Figure PCTCN2018123373-appb-000003
Figure PCTCN2018123373-appb-000004
注：表格中的组件指的是太阳能电池。
以上对本发明做了详尽的描述，其目的在于让熟悉此领域技术的人士能够了解本发明的内容并加以实施，并不能以此限制本发明的保护范围，凡根据本发明的精神实质所作的等效变化或修饰，都应涵盖在本发明的保护范围内。

Claims (20)

  1. 一种太阳能电池用封装胶膜，其特征在于：包括与电池片相接触的透明层、与所述的透明层相接触的第一胶膜层，
    所述的第一胶膜层的原料包括如下组分：质量比为3～25:1的树脂和有色填料、占所述的树脂和所述的有色填料总质量0.1％～5％的交联剂、占所述的树脂和所述的有色填料总质量0.1％～1％的助交联剂、占所述的树脂和所述的有色填料总质量0.1％～1％的偶联剂、占所述的树脂和所述的有色填料总质量0.1％～1％的光稳定剂、占所述的树脂和所述的有色填料总质量0.1％～5％的光引发剂。
  2. 根据权利要求1所述的太阳能电池用封装胶膜，其特征在于：所述的第一胶膜层中所述的树脂和所述的有色填料的质量比为3～5:1。
  3. 根据权利要求1所述的太阳能电池用封装胶膜，其特征在于：所述的太阳能电池用封装胶膜还包括与所述的背板或玻璃相接触的第二胶膜层。
  4. 根据权利要求3所述的太阳能电池用封装胶膜，其特征在于：所述的太阳能电池用封装胶膜还包括设置在所述的第一胶膜层和所述的第二胶膜层之间的一层或几层第三胶膜层。
  5. 根据权利要求3所述的太阳能电池用封装胶膜，其特征在于：所述的第二胶膜层的原料包括质量比为15～25:1的树脂和有色填料。
  6. 根据权利要求5所述的太阳能电池用封装胶膜，其特征在于：所述的第二胶膜层的原料还包括占所述的树脂和所述的有色填料总质量0.1％～5％的交联剂、占所述的树脂和所述的有色填料总质量0.1％～1％的助交联剂、占所述的树脂和所述的有色填料总质量0.1％～1％的偶联剂、占所述的树脂和所述的有色填料总质量0.1％～1％的光稳定剂。
  7. 根据权利要求1所述的太阳能电池用封装胶膜，其特征在于：所述的透明层的厚度为20～60微米。
  8. 根据权利要求1所述的太阳能电池用封装胶膜，其特征在于：所述的透明层的原料包括如下组分：树脂、占所述的树脂质量0.1％～5％的交联剂、占所述的树脂质量0.1％～1％的助交联剂、占所述 的树脂质量0.1％～1％的偶联剂、占所述的树脂质量0.1％～1％的光稳定剂。
  9. 根据权利要求1至8中任一项所述的太阳能电池用封装胶膜，其特征在于：所述的树脂为选自EVA、POE、PVB中的一种或几种。
  10. 根据权利要求1至8中任一项所述的太阳能电池用封装胶膜，其特征在于：所述的有色填料为选自钛白粉、碳酸钙、二氧化硅、三氧化二铝、锌钛白中的一种或几种。
  11. 根据权利要求1至8中任一项所述的太阳能电池用封装胶膜，其特征在于：所述的光引发剂为选自2-羟基-2-甲基-1-苯基-1-丙酮、1-羟基环己基苯基甲酮、二苯甲酮、(2,4,6-三甲基苯甲酰基)二苯基氧化膦、2-苄基-2-二甲基氨基-1-(4-吗啉苯基)丁酮、2-羟基-1-(4-(2-羟基-2-甲基丙酰基苯基)苄基)-2-甲基-1-丙酮、大分子光引发剂硫杂蒽酮类、以及可见光引发剂樟脑琨中的一种或几种。
  12. 根据权利要求1至8中任一项所述的太阳能电池用封装胶膜，其特征在于：所述的交联剂为选自交联剂过氧化2-乙基己基碳酸叔丁酯、叔丁基过氧化-异丙基碳酸酯、过氧化二苯甲酰、过氧化二异丙苯、2,5-二甲基-2,5-双(叔丁基过氧基)己烷、过氧化环己酮、叔丁基过氧化氢、过氧苯甲酸叔丁酯、过氧乙酸叔丁酯、过氧重碳酸二-(4-叔丁基环己基)酯、叔丁基过氧化-3,5,5-三甲基己酸酯、三烯丙基异氰酸酯中的一种或几种。
  13. 根据权利要求1至8中任一项所述的太阳能电池用封装胶膜，其特征在于：所述的助交联剂为选自三羟甲基丙烷三丙烯酸酯、2-三羟甲基丙烷四丙烯酸酯、乙氧化三羟甲基丙烷三丙烯酸酯、乙氧化三羟甲基丙烷三丙烯酸酯、丙氧化三羟甲基丙烷三丙烯酸酯中的一种或几种。
  14. 根据权利要求1至8中任一项所述的太阳能电池用封装胶膜，其特征在于：所述的偶联剂为选自3-甲基丙烯酰氧基丙基甲基三甲氧基硅烷、3-缩水甘油丙基三甲氧基硅烷、乙烯基三甲氧基硅烷、3-氨丙基三乙氧基硅烷、乙烯基三甲氧基硅烷中的一种或几种。
  15. 根据权利要求1至8中任一项所述的太阳能电池用封装胶膜，其特征在于：所述的光稳定剂为选自双(2,2,6,6-四甲基-4-哌啶基)癸二酸酯、聚丁二酸(4-羟基-2,2,6，6-四甲基-1-哌啶乙醇)酯、聚-{[6-[(1,1,3,3-四甲基丁基)-亚氨基]-1,3,5-三嗪-2，4-二基][2-(2,2,6,6-四甲基哌啶基)-氮基]-亚已基-[4-(2,2,6,6-四甲基哌啶基)-氨基]中的一种或几种。
  16. 一种如权利要求1至15中任一项所述的太阳能电池用封装胶膜的制备方法，其特征在于：包括依次进行的如下步骤：
    步骤(1)、将所述的第一胶膜层胶膜层和所述的透明层的原料分别配制好后，通过挤出机流延成膜；
    步骤(2)、在所述的透明层所在侧，通过UV灯照射使得UV穿过透明层到达所述的第一胶膜层并促使所述的第一胶膜层的表面发生交联反应；
    步骤(3)、冷却后牵引收卷制得所述的太阳能电池用封装胶膜。
  17. 根据权利要求16所述的制备方法，其特征在于：步骤(1)的加工温度为60～110℃。
  18. 根据权利要求16所述的制备方法，其特征在于：步骤(3)中，通过三辊定型后冷却收卷。
  19. 根据权利要求16所述的制备方法，其特征在于：步骤(3)中的冷却温度为20～50℃。
  20. 一种如权利要求1至15中任一项所述的太阳能电池用封装胶膜在太阳能电池中的应用。
PCT/CN2018/123373 2017-12-27 2018-12-25 一种太阳能电池用封装胶膜及其制备方法和应用 Ceased WO2019128962A1 (zh)

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