JP5719726B2 - Front protective sheet for solar cell and solar cell module produced using the same - Google Patents

Description

  TECHNICAL FIELD The present invention relates to a front protective sheet used as a front protective member for a solar battery cell, and in particular, comprises a resin layer having both flexibility, moisture resistance and weather resistance, and is effective in reducing the weight and durability of solar cells. The present invention relates to a solar cell front protective sheet and a lightweight and highly durable solar cell using the solar cell front protective sheet.

In recent years, solar cells that directly convert sunlight into electric energy have attracted attention and are being developed from the viewpoint of effective use of resources and prevention of environmental pollution. The solar cell is configured such that the solar cell is sealed with a sealing film such as an ethylene-vinyl acetate copolymer, polyethylene, or polypropylene film between the front surface protection sheet and the back surface protection sheet from the light receiving surface side.
Such a solar cell is usually manufactured by laminating a front protective sheet, a sealing film, a power generation element, a sealing film, and a back protective sheet in this order and bonding them together by heating and melting. As a front protective sheet for solar cells, it is required to have excellent durability against ultraviolet rays. In addition, in order to prevent rusting of internal conductors and electrodes due to moisture or water permeation, it is excellent in moisture resistance. Is an extremely important requirement. For this reason, conventionally, a glass plate has been used as the surface-side transparent protective member. However, the glass plate is excellent in light resistance and moisture resistance, but has a drawback that it is heavy and weak against impact and easily cracked. To solve this problem, for example, Patent Document 1 uses a transparent resin film to solve the problem of breakage due to weight and impact, and by combining a resin film with good weather resistance and moisture resistance, durability of the solar cell is improved. A solar cell front protective sheet effective for improving the performance has been proposed.
However, in the solar cell front protective sheet described in Patent Document 1, when the weathering layer and the moisture-proof layer are bonded together using an adhesive, it is difficult to increase the thickness of the adhesive from the viewpoint of productivity. In some cases, the moisture-proof layer is damaged by falling objects and the moisture-proof function is deteriorated.

On the other hand, without using an adhesive, ethylene-vinyl acetate copolymer, which is generally used for sealing materials for solar electronics, is used as a film that bonds the weather-proof layer and moisture-proof layer. A method for preventing this has been proposed (Patent Document 2).
However, when an ethylene-vinyl acetate copolymer is used, since the crosslinking is usually performed using a crosslinking agent such as an organic peroxide for the purpose of imparting heat resistance to the copolymer, the surface accompanying the crosslinking is used. Deterioration of appearance and deterioration of moisture-proof layer occur. In addition, the ethylene-vinyl acetate copolymer contains an acetic acid, a crosslinking agent, a crosslinking aid, etc. generated by hydrolysis of the ethylene-vinyl acetate copolymer during long-term use. There was a problem that the resin layer and the adhesive were deteriorated and peeling at the interface in the layer occurred.
Further, a solar cell encapsulant made of an α-olefin polymer that does not require crosslinking and does not generate acetic acid (Patent Document 3), a polymer made of at least one polyolefin copolymer and at least one crystalline polyolefin A solar cell encapsulating material (Patent Document 4) comprising a blend or a polymer alloy is disclosed. In particular, the above Patent Document 4 specifically describes a polymer blend of a low melting point ethylene-vinyl acetate copolymer and a high melting point ethylene-vinyl acetate copolymer (see Example 1), ethylene-methacrylic acid copolymer. Polymer blends of coalesced and general purpose crystalline polyethylene (see Example 2) and polymer blends of ethylene-methyl acrylate copolymer and general purpose crystalline polypropylene (see Example 3) are disclosed.
However, the resin composition comprising a polymer mainly composed of propylene specifically used in Patent Document 3 has insufficient transparency (total light transmittance: 83.2% (see Examples). ))) When used as a laminated film in the front protective sheet, the light transmittance of the entire front protective sheet is lowered, and the power generation efficiency of the solar cell is lowered. Further, each polymer blend used in Patent Document 4 is not necessarily excellent in transparency, and there is still a problem in balancing the flexibility, heat resistance and transparency.
In any of the above Patent Documents 3 and 4, it is said that the moisture-proof layer in the front protective sheet is prevented from being deteriorated, thereby having long-term high moisture resistance and weather resistance and improving the durability of the solar cell. There is no eye. Thus, in the conventional technology relating to the entire solar cell protective sheet, no useful solution to the deterioration of the moisture-proof layer in the front protective sheet has been proposed.

Japanese Patent No. 3978911 Japanese Patent No. 3978912 JP 2006-210905 A JP 2001-332750 A

That is, an object of the present invention is to solve the above-mentioned conventional problems in a protective sheet used as a transparent protective member for a solar cell, and to prevent deterioration of a resin layer having a moisture-proof performance constituting a part of the sheet. By having a resin layer with a good balance between flexibility, heat resistance and transparency, it prevents deterioration of the moisture resistance of the front protective sheet due to falling objects, etc., and transparency and long-term high moisture resistance An object of the present invention is to provide a solar cell front protective sheet that has weather resistance and is effective in reducing the weight and durability of solar cells.
Moreover, the subject of this invention is providing the lightweight and highly durable solar cell module and solar cell using this front protective sheet for solar cells.

As a result of intensive studies, the present inventors have obtained a resin layer containing an ethylene-α-olefin random copolymer having specific thermal characteristics and an ethylene-α-olefin block copolymer having specific thermal characteristics. By using it for the front protective sheet for solar cells, it was found that flexibility, heat resistance and transparency can be satisfied at the same time, and the present invention has been completed.
That is, the present invention
The weather-resistant layer (A) and the moisture-proof layer (B), the ethylene-α-olefin random copolymer (C-1) that satisfies the following condition (1) and the ethylene-α that satisfies the following condition (2): -It is related with the solar cell front protective sheet characterized by laminating | stacking through the soft layer (C) containing an olefin block copolymer (C-2).
(1) The heat of crystal fusion measured at a heating rate of 10 ° C./min in differential scanning calorimetry is 0 to 70 J / g.
(2) The crystal melting peak temperature measured at a heating rate of 10 ° C./min in differential scanning calorimetry is 100 ° C. or higher, and the crystal melting heat amount is 5 to 70 J / g.

  Moreover, this invention relates to the solar cell module and solar cell which were produced using the front surface protection sheet for solar cells of the said this invention.

  According to the present invention, in the front protective sheet, by setting the flexible layer constituting the sheet to a specific configuration, the flexibility of the flexible layer can be balanced with heat resistance and transparency. This prevents the deterioration of the moisture-proof performance of the front sheet caused by the deterioration of the moisture-proof layer due to falling objects, etc., which combines transparency and long-term high moisture resistance and weather resistance, and makes the solar cell lighter and more durable It is possible to provide a solar cell front protective sheet effective for improving the solar cell performance, and a lightweight and highly durable solar cell module and solar cell using the solar cell front protective sheet.

It is a schematic sectional drawing which shows an example of embodiment of the front protective sheet for solar cells of this invention. It is a schematic sectional drawing which shows an example of the solar cell module of this invention.

Hereinafter, the present invention will be described in more detail. In the present specification, the term “layer” may include the meaning of “film”.
<Weather-resistant layer (A)>
The weathering layer (A) in the present invention refers to a resin layer that is highly transparent and flexible, and has excellent heat resistance, moisture resistance and UV durability, and is intended to maintain the solar cell front protective sheet and surface appearance. Used as
The weather resistance of the weather resistant layer is preferably such that there is little decrease in mechanical properties and total light transmittance in a weather resistance test conducted according to JIS K7350, and mechanical properties and total light transmittance after 5000 hours have passed. Are preferable, and those having no decrease in mechanical properties and total light transmittance after 10000 hours are particularly preferable.
Examples of the material of the weather resistant layer (A) include polytetrafluoroethylene (PTFE), 4-fluorinated ethylene-perchloroalkoxy copolymer (PFA), and 4-fluorinated ethylene-6-fluorinated propylene copolymer. Fluororesin layers such as (FEP), 2-ethylene-4-fluoroethylene copolymer (ETFE), poly-3-fluoroethylene chloride (PCTFE), polyvinylidene fluoride (PVDF), and polyvinyl fluoride (PVF); Alternatively, a film obtained by forming a resin composition in which an ultraviolet absorber is kneaded into a resin such as acrylic, polycarbonate, polyethylene terephthalate (PET), or polyethylene naphthalate (PEN) is preferably used, and long-term durability and high light transmittance are used. From the viewpoint of 2-ethylene-4-fluoroethylene copolymer (ETFE), 4-fluoroethylene 6-fluorinated propylene copolymer (FEP) is more preferably used. In addition, as said ultraviolet absorber, the thing similar to the below-mentioned ultraviolet absorber which can be contained in a flexible layer can be used. Although the said resin can also be used by 1 type, it can also be used in combination of 2 or more type.

  The thickness of the weather-resistant layer (A) is generally about 20 to 200 μm, preferably 30 to 120 μm, more preferably 40 to 80 μm from the viewpoint of film handling and cost.

<Dampproof layer (B)>
The moisture-proof layer (B) in the present invention is a resin layer that is used to prevent moisture, internal conductors due to permeation of water, rusting of electrodes, and the like, and preferably is a highly transparent resin layer with excellent moisture resistance. Although there is no particular limitation, those having at least one inorganic oxide coating film on at least one surface of the base material layer are preferably used.
The base material layer is preferably a thermoplastic polymer film, preferably highly transparent, and any material that can be used for ordinary packaging materials can be used without particular limitation. Specifically, polyolefins such as homopolymers or copolymers such as ethylene, propylene and butene, amorphous polyolefins such as cyclic polyolefins, polyesters such as polyethylene terephthalate (PET) and polyethylene naphthalate (PEN), nylon 6 , Nylon 66, nylon 12, polyamide such as copolymer nylon, ethylene-vinyl acetate copolymer partial hydrolyzate (EVOH), polyimide, polyetherimide, polysulfone, polyethersulfone, polyetheretherketone, polycarbonate, polyvinyl Examples include butyral, polyarylate, fluororesin, acrylate resin, and biodegradable resin. Among these, at least one resin selected from polyester, polyamide, and polyolefin is preferable from the viewpoint of film physical properties, cost, and the like. Among these, polyethylene terephthalate (PET) and polyethylene naphthalate (PEN) are particularly preferable from the viewpoint of film properties.

In addition, the base material layer is a known additive such as an antistatic agent, a light blocking agent, an ultraviolet absorber, a plasticizer, a lubricant, a filler, a colorant, a stabilizer, a lubricant, a crosslinking agent, an antiblocking agent, An antioxidant etc. can be contained.
The thermoplastic polymer film as the base material layer is formed by using the above raw materials, but when used as a base material, it may be unstretched or stretched. Good. Moreover, you may laminate | stack with the other plastic base material.

  Such a base material layer can be produced by a conventionally known method. For example, the raw material resin is melted by an extruder, extruded by an annular die or a T die, and rapidly cooled to be oriented substantially amorphously. No unstretched film can be produced. Further, by using a multilayer die, it is possible to produce a single layer film made of one kind of resin, a multilayer film made of one kind of resin, a multilayer film made of various kinds of resins, and the like.

  The unstretched film is subjected to a known method such as uniaxial stretching, tenter sequential biaxial stretching, tenter simultaneous biaxial stretching, tubular simultaneous biaxial stretching, or the like. A film stretched in at least a uniaxial direction can be produced by stretching in a direction (horizontal axis) perpendicular thereto. Although a draw ratio can be set arbitrarily, it is preferable that 150 degreeC heat shrink rate is 0.01 to 5%, Furthermore, it is preferable that it is 0.01 to 2%. Among these, from the viewpoint of film properties, a biaxially stretched polyethylene naphthalate film, a polyethylene terephthalate and / or a coextruded biaxially stretched film of polyethylene naphthalate and other plastics are preferable.

  In addition, it is preferable to apply | coat an anchor coating agent to the said base material layer for the adhesive improvement with an inorganic thin film. As anchor coating agents, solvent-based or water-soluble polyester resins, isocyanate resins, urethane resins, acrylic resins, vinyl-modified resins, vinyl alcohol resins, vinyl butyral resins, ethylene vinyl alcohol resins, nitrocellulose resins, oxazoline group-containing resins, carbodiimides A group-containing resin, a methylene group-containing resin, an epoxy group-containing resin, a modified styrene resin, a modified silicon resin, an alkyl titanate, or the like can be used alone or in combination of two or more. Also contains silane coupling agents, titanium coupling agents, light blocking agents, ultraviolet absorbers, stabilizers, lubricants, antiblocking agents, antioxidants, etc., or they are copolymerized with the above resins Things can be used.

  As a method for forming the anchor coat layer, a known coating method is appropriately adopted. For example, any method such as a reverse roll coater, a gravure coater, a rod coater, an air doctor coater, a spray or a coating method using a brush can be used. Alternatively, the vapor deposition layer may be immersed in a resin solution. After application, the solvent can be evaporated using a known drying method such as hot drying such as hot air drying or hot roll drying at a temperature of about 80 to 200 ° C., or infrared drying. Moreover, in order to improve water resistance and durability, the crosslinking process by electron beam irradiation can also be performed. Further, the formation of the anchor coat layer may be a method performed in the middle of the base material layer production line (in-line) or a method performed after the base material layer is manufactured (off-line).

  As a moisture-proof layer, a substrate in which a coating film of a metal such as aluminum is formed on the base material layer is known. However, when a metal such as aluminum is applied to a solar cell, current may leak. Therefore, an inorganic oxide coating film such as silica / alumina is preferably used.

  As a method for forming the inorganic oxide coating film, any method such as a vapor deposition method and a coating method can be used, but a vapor deposition method is preferable in that a uniform thin film having a high gas barrier property can be obtained. This vapor deposition method includes methods such as physical vapor deposition (PVD) or chemical vapor deposition (CVD). Examples of physical vapor deposition include vacuum deposition, ion plating, and sputtering, and chemical vapor deposition includes plasma CVD using plasma and a catalyst that thermally decomposes a material gas using a heated catalyst body. Examples include chemical vapor deposition (Cat-CVD).

  Examples of the inorganic substance constituting the inorganic oxide coating film include silicon, aluminum, magnesium, zinc, tin, nickel, titanium, amorphous carbon, and the like, oxides, carbides, nitrides, or mixtures thereof. However, diamond-like carbon mainly composed of silicon oxide, aluminum oxide, and amorphous carbon is preferable. In particular, silicon oxide, silicon nitride, silicon oxynitride, and aluminum oxide are preferable in that high gas barrier properties can be stably maintained.

  The thickness of the coating film is preferably 40 to 1000 nm, more preferably 80 to 800 nm, and still more preferably 160 to 600 nm from the viewpoint of stable moistureproof performance. Moreover, generally the thickness of the said base material layer is about 5-100 micrometers, 8-50 micrometers is preferable from the point of productivity or the ease of handling, and 12-25 micrometers is still more preferable. Therefore, the thickness of the moisture-proof layer (A) is generally about 6 to 100 μm, preferably 9 to 50 μm, more preferably 12 to 25 μm from the viewpoint of productivity and ease of handling.

<Flexible layer (C)>
The flexible layer (C) in the present invention is used for the purpose of laminating the weather-resistant layer (A) and the moisture-proof layer (B) through this. As the flexible layer (C), specifically, a film made of an ethylene-α-olefin copolymer is used because it is highly transparent, rich in flexibility, and excellent in heat resistance and hydrolyzability. It is possible to use a resin composition containing an ethylene-α-olefin random copolymer having specific thermal characteristics and an ethylene-α-olefin block copolymer having specific thermal characteristics. This is necessary from the viewpoint of developing flexibility.

Here, the ethylene-α-olefin random copolymer having specific thermal characteristics is an ethylene-α-olefin random copolymer (C-1) that satisfies the following condition (1), and has specific thermal characteristics. The ethylene-α-olefin block copolymer has an ethylene-α-olefin block copolymer (C-2) that satisfies the following condition (2).
(1) The heat of crystal fusion measured at a heating rate of 10 ° C./min in differential scanning calorimetry is 0 to 70 J / g.
(2) The crystal melting peak temperature measured at a heating rate of 10 ° C./min in differential scanning calorimetry is 100 ° C. or higher, and the crystal melting heat amount is 5 to 70 J / g.

  The heat resistance of the front protective sheet for solar cells is the characteristics of the ethylene-α-olefin random copolymer (C-1) constituting the flexible layer (C) (crystal melting peak temperature, crystal melting heat, MFR, molecular weight, etc.) And ethylene-α-olefin block copolymer (C-2), which are affected by various properties (crystal melting peak temperature, crystal melting heat, MFR, molecular weight, etc.). The crystal melting peak temperature of (C-2) is strongly influenced.

  Generally, a solar cell module is heated to about 85 to 90 ° C. due to heat generated during power generation or radiant heat of sunlight, but the ethylene-α-olefin block copolymer (C— in the flexible layer (C)). If the crystal melting peak temperature of 2) is 100 ° C. or higher, the heat resistance of the solar cell front protective sheet of the present invention can be ensured. On the other hand, if the upper limit temperature of the crystal melting peak temperature of the ethylene-α-olefin block copolymer (C-2) is 145 ° C., the sealing can be performed without increasing the temperature in the solar cell element sealing step. This is preferable because it is possible. In addition, if the heat of crystal melting of each of the ethylene-α-olefin random copolymer (C-1) and the ethylene-α-olefin block copolymer (C-2) in the flexible layer (C) is within a specified range. The flexibility and transparency (total light transmittance) of the front protective sheet for solar cells of the present invention are ensured, and problems such as blocking of raw material pellets are also unlikely to occur.

Kind of α-olefin used in each of ethylene-α-olefin random copolymer (C-1) and ethylene-α-olefin block copolymer (C-2) constituting flexible layer (C) in the present invention May be the same or different, but in the present invention, the same is the compatibility when mixed and the transparency of the front protective sheet for solar cells, that is, the solar cell. It is preferable because photoelectric conversion efficiency is improved.
Next, the mixing (containing) mass ratio of these copolymers in the flexible layer (C) is not particularly limited, but preferably (C-1) / (C-2) = 99 to 50 /. 1-50, More preferably, it is 98-60 / 2-40, More preferably, it is 97-70 / 3-30. However, the total of (C-1) and (C-2) is 100 parts by mass. Here, it is preferable if the mixing (containing) mass ratio is in the above range because a flexible layer (C) having an excellent balance of flexibility, heat resistance, transparency and the like can be easily obtained.

  The flexibility of the flexible layer (C) in the present invention may be appropriately adjusted in consideration of the shape, thickness, installation location, etc. of the applied solar cell. For example, the vibration frequency in dynamic viscoelasticity measurement is 10 Hz, temperature The storage elastic modulus (E ′) at 20 ° C. is preferably 1 to 2000 MPa. From the viewpoint of protection of the solar cell element, the storage elastic modulus (E ′) is preferably lower. However, handling properties and blocking between the sheet surfaces when the flexible layer (C) of the present invention is collected in a sheet shape or the like. Considering prevention and the like, it is more preferably 3 to 1000 MPa, further preferably 5 to 500 MPa, and particularly preferably 10 to 100 MPa.

The heat resistance of the flexible layer (C) in the present invention is determined by various characteristics of the ethylene-α-olefin random copolymer (C-1) (crystal melting peak temperature, crystal melting heat amount, MFR, molecular weight, etc.) and ethylene-α-. Although it is influenced by various properties (crystal melting peak temperature, crystal melting heat, MFR, molecular weight, etc.) of the olefin block copolymer (C-2), in particular, ethylene-α-olefin block copolymer (C-2) The crystal melting peak temperature is strongly affected.
As described above, if the crystal melting peak temperature of the ethylene-α-olefin block copolymer (C-2) in the flexible layer (C) is 100 ° C. or higher, the heat resistance of the flexible layer (C) in the present invention is ensured. I can do it. And since the heat resistance and elastic modulus of the flexible layer (C) of the solar cell front protective sheet of the present invention are the lowest among the layers constituting the member, the heat resistance of the solar cell front protective sheet of the present invention is the flexible layer ( C) determines its performance.
In the present invention, the heat resistance of the flexible layer (C) is 0 mm between white plate glass having a thickness of 3 mm (size: length 75 mm, width 25 mm) and an aluminum plate having a thickness of 5 mm (size: length 120 mm, width 60 mm). .5mm sheet-like flexible layer (C) is stacked, and a sample is laminated and pressed using a vacuum press machine at 150 ° C for 15 minutes, and the sample is inclined at 60 ° C in a 100 ° C constant temperature bath. Then, after observing the state after 500 hours, the case where the glass did not deviate from the initial reference position was evaluated as ◯, and the case where the glass deviated from the initial reference position or the sheet was melted was evaluated as x.

  The total light transmittance of the flexible layer (C) in the present invention is not so much when applied to a type of solar cell to be applied, for example, an amorphous thin film silicon type or a portion that does not block sunlight reaching the solar electronic element. Although it may not be regarded as important, it is usually preferably 85% or more, more preferably 87% or more, taking into consideration the photoelectric conversion efficiency of the solar cell and handling properties when various members are superimposed, 90% % Or more is more preferable.

  About the softness | flexibility of the flexible layer (C) in this invention, heat resistance, and transparency, it becomes a contradictory property easily. Specifically, if the crystallinity of the resin composition used for improving flexibility is excessively lowered, the heat resistance is lowered and becomes insufficient. On the other hand, if the crystallinity of the resin composition used for improving the heat resistance is excessively improved, the transparency is lowered and becomes insufficient. In the present invention, the balance is used as an index of flexibility, the vibration frequency is 10 Hz in dynamic viscoelasticity measurement, the storage elastic modulus (E ′) at a temperature of 20 ° C., and the heating rate is 10 ° C. in differential scanning calorimetry as an index of heat resistance. When the total light transmittance is used as an index of crystal melting peak temperature and transparency measured in / min, three indexes are storage elastic modulus (E ′) of 1 to 2000 MPa, and crystal melting peak temperature is 100 ° C. or higher. The total light transmittance is preferably 85% or more, the storage elastic modulus (E ′) is 5 to 500 MPa, the crystal melting peak temperature is 105 to 145 ° C., and the total light transmittance is more preferably 85% or more. It is particularly preferable that the storage elastic modulus (E ′) is 10 to 100 MPa, the crystal melting peak temperature is 110 to 145 ° C., and the total light transmittance is 87% or more.

  The flexible layer (C) has a thickness of about 50 to 100 μm, preferably 150 to 750 μm, more preferably 300 to 500 μm from the viewpoint of handling.

  The melt flow rate (MFR) of the ethylene-α-olefin random copolymer (C-1) used in the present invention is not particularly limited, but usually MFR (JIS K7210, temperature: 190 ° C., load) : 21.18N) is about 0.5 to 100 g / 10 min, preferably 2 to 50 g / 10 min, more preferably 3 to 30 g / 10 min. Here, the MFR may be selected in consideration of the formability when the sheet is formed. For example, when calendering a sheet, the MFR is preferably a relatively low value, specifically about 0.5 to 5 g / 10 min from the handling property when the sheet is peeled off from the molding roll. When the extrusion molding is performed using MFR, the MFR is preferably 2 to 50 g / 10 min, more preferably 3 to 30 g / 10 min, from the viewpoint of reducing the extrusion load and increasing the extrusion amount.

The ethylene-α-olefin random copolymer (C-1) used in the present invention has a heat of crystal melting of 0 to 70 J / g measured at a heating rate of 10 ° C./min in the condition (1) differential scanning calorimetry. It is important to satisfy, preferably 5 to 70 J / g, more preferably 10 to 65 J / g. If it is in this range, since the softness | flexibility, transparency (total light transmittance), etc. of the solar cell sealing material of this invention are ensured, it is preferable. Moreover, it is preferable if the heat of crystal fusion is 0 J / g or more because problems such as blocking of raw material pellets are unlikely to occur. Here, as reference values for the heat of crystal fusion, general-purpose high-density polyethylene (HDPE) is about 170 to 220 J / g, and low-density polyethylene resin (LDPE) and linear low-density polyethylene (LLDPE) are 100 to 160 J. / G or so.
Further, the crystal melting peak temperature of the ethylene-α-olefin random copolymer (C-1) used in the present invention is not particularly limited, but is usually less than 100 ° C., preferably 30 to 90. ° C. Here, as reference values for the crystal melting peak temperature, general-purpose high-density polyethylene (HDPE) is about 130 to 145 ° C., and low-density polyethylene resin (LDPE) and linear low-density polyethylene (LLDPE) are 100 to 125. It is about ℃. That is, in the ethylene-α-olefin random copolymer (C-1) used alone in the present invention, the crystal melting peak temperature measured at a heating rate of 10 ° C./min in differential scanning calorimetry is 100 ° C. or higher, In addition, it is difficult to achieve a crystal heat of fusion of 5 to 70 J / g.

  Specific examples of the ethylene-α-olefin random copolymer (C-1) used in the present invention include trade names “engage”, “affinity” manufactured by Dow Chemical Co., Ltd., Mitsui Examples include trade names “TAFMER A”, “TAFMER P” manufactured by Kagaku Co., Ltd., trade names “Kernel” manufactured by Nippon Polyethylene Co., Ltd., and the like.

  The melt flow rate (MFR) of the ethylene-α-olefin block copolymer (C-2) used in the present invention is not particularly limited, but usually MFR (JIS K7210, temperature: 190 ° C., load) : 21.18N) is about 0.5 to 100 g / 10 min, more preferably 1 to 50 g / 10 min, still more preferably 1 to 30 g / 10 min, and particularly preferably 1 to 10 g / 10 min.

  The ethylene-α-olefin block copolymer (C-2) used in the present invention has a crystal melting peak temperature of 100 ° C. or higher measured at a heating rate of 10 ° C./min in differential scanning calorimetry, and has a crystal structure. It is important that the heat of fusion satisfies 5 to 70 J / g (condition (2)). The crystal melting peak temperature is preferably 105 ° C. or higher, more preferably 110 ° C. or higher, and the upper limit is usually 145 ° C. The heat of crystal fusion is preferably 10 to 60 J / g, more preferably 15 to 55 J / g.

  The block structure of the ethylene-α-olefin block copolymer (C-2) used in the present invention is not particularly limited as long as the condition (2) described above is satisfied, but flexibility, heat resistance, Two or more, preferably three or more segments or blocks having different comonomer contents, crystallinity, density, crystal melting peak temperature (melting point Tm), or glass transition temperature (Tg) from the viewpoint of balancing such as transparency A multi-block structure containing Specific examples include a completely symmetric block, an asymmetric block, and a taper block structure (a structure in which the ratio of the block structure gradually increases in the main chain). Regarding the structure and production method of the copolymer having the multi-block structure, International Publication No. 2005/090425 (WO2005 / 090425), International Publication No. 2005/090426 (WO2005 / 090426), and International Publication No.2005. / 090427 pamphlet (WO2005 / 090427) or the like can be employed.

In the present invention, the ethylene-α-olefin block copolymer having the multi-block structure will be described in detail below.
The ethylene-α-olefin block copolymer having a multiblock structure can be suitably used in the present invention, and an ethylene-octene multiblock copolymer having 1-octene as a copolymerization component as an α-olefin is preferable. As the block copolymer, an almost non-crystalline soft segment copolymerized with a large amount of octene component (about 15 to 20 mol%) with respect to ethylene and a small amount of octene component with respect to ethylene (about 2 mol%) Less) a multiblock copolymer in which two or more highly crystalline hard segments each having a copolymerized crystal melting peak temperature of 110 to 145 ° C. are present. By controlling the chain length and ratio of these soft segments and hard segments, both flexibility and heat resistance can be achieved.
As a specific example of the copolymer having the multi-block structure, trade name “Infuse” manufactured by Dow Chemical Co., Ltd. may be mentioned.

  The melt flow rate (MFR) of the ethylene-α-olefin block copolymer (C-2) used in the present invention is not particularly limited, but usually MFR (JIS K7210, temperature: 190 ° C., load) : 21.18N) is about 0.5 to 100 g / 10 min, more preferably 1 to 50 g / 10 min, still more preferably 1 to 30 g / 10 min, and particularly preferably 1 to 10 g / 10 min.

  Here, the MFR may be selected in consideration of the formability when the sheet is formed. Specifically, when the sheet is calendered, the MFR is preferably relatively low, specifically about 0.5 to 5 g / 10 min from the handling property when the sheet is peeled off from the forming roll, In the case of extrusion molding using a T-die, a MFR of 1 to 30 g / 10 min is preferably used from the viewpoint of reducing the extrusion load and increasing the extrusion amount. Furthermore, from the viewpoint of adhesion and ease of wraparound when sealing a solar cell element (cell), a MFR of 3 to 50 g / 10 min is preferably used.

  Next, the contents of the ethylene-α-olefin random copolymer (C-1) and the ethylene-α-olefin block copolymer (C-2) in the flexible layer (C) are flexibility, heat resistance, From the viewpoint of having an excellent balance such as transparency, it is preferably 50 to 99% by mass and 1 to 50% by mass, more preferably 60 to 98% by mass and 2 to 40% by mass, respectively. Preferably, they are 70-97 mass% and 3-30 mass%.

<Front protective sheet for solar cell and method for producing the same>
The solar cell front protective sheet of the present invention further improves various physical properties (flexibility, heat resistance, transparency, adhesiveness, etc.), molding processability, economical efficiency and the like without departing from the gist of the present invention. Resins other than the ethylene-α-olefin random copolymer (C-1) and the ethylene-α-olefin block copolymer (C-2) described above can be mixed for the purpose. Examples of the resin include other polyolefin resins and various elastomers (olefin-based, styrene-based, etc.), polar groups such as carboxyl groups, amino groups, imide groups, hydroxyl groups, epoxy groups, oxazoline groups, thiol groups, silanol groups, and the like. And a resin modified with a tackifier resin.

Examples of the tackifying resin include petroleum resins, terpene resins, coumarone-indene resins, rosin resins, and hydrogenated derivatives thereof. Specifically, as the petroleum resin, there are an aromatic petroleum resin from alicyclic petroleum resins and C ₉ components from cyclopentadiene or dimer thereof, terpene resins and terpene from The terpene resin β- pinene -Phenol resin and rosin resin include rosin resins such as gum rosin and wood rosin, and esterified rosin resins modified with glycerin and pentaerythritol. Further, the tackifying resin can be obtained mainly having various softening temperatures depending on the molecular weight, but the compatibility when mixed with the copolymer (C-1) and the copolymer (C-2) described above. From the viewpoints of color tone and thermal stability, a hydrogenated derivative of an alicyclic petroleum resin having a softening temperature of 100 to 150 ° C., preferably 120 to 140 ° C. is particularly preferable. When the resin other than the copolymer (C-1) and the copolymer (C-2) described above is mixed, usually, when the resin composition is 100 parts by mass, 20 parts by mass or less is preferable, and 10 parts by mass. Part or less is more preferable.

  Moreover, various additives can be added to the front protective sheet for solar cells of the present invention as necessary. Examples of the additive include a silane coupling agent, an antioxidant, an ultraviolet absorber, a weathering stabilizer, a light diffusing agent, a nucleating agent, a pigment (for example, a white pigment), a flame retardant, and a discoloration preventing agent. . In the present invention, it is preferable that at least one additive selected from a silane coupling agent, an antioxidant, an ultraviolet absorber, and a weathering stabilizer is added for reasons described later. In the present invention, for example, when a high heat resistance is required, a crosslinking agent and / or a crosslinking aid may be blended.

  Examples of silane coupling agents include compounds having a hydrolyzable group such as an alkoxy group together with an unsaturated group such as a vinyl group, an acryloxy group or a methacryloxy group, an amino group or an epoxy group. . Specific examples of the silane coupling agent include N- (β-aminoethyl) -γ-aminopropyltrimethoxysilane, N- (β-aminoethyl) -γ-aminopropylmethyldimethoxysilane, and γ-aminopropyltriethoxy. Examples include silane, γ-glycidoxypropyltrimethoxysilane, γ-methacryloxypropyltrimethoxysilane, and the like. In the present invention, γ-glycidoxypropyltrimethoxysilane and γ-methacryloxypropyltrimethoxysilane are preferably used because of good adhesiveness and little discoloration such as yellowing. The addition amount of this silane coupling agent is about 0.1-5 mass% normally in the front surface protection sheet for solar cells, and it is preferable to add 0.2-3 mass%. In addition, similar to the silane coupling agent, a coupling agent such as an organic titanate compound can be effectively used.

  As the antioxidant, various commercially available products can be applied, and various types such as monophenol type, bisphenol type, polymer type phenol type, sulfur type and phosphite type can be exemplified. Examples of monophenols include 2,6-di-tert-butyl-p-cresol, butylated hydroxyanisole, 2,6-di-tert-butyl-4-ethylphenol, and the like. Examples of bisphenols include 2,2′-methylene-bis- (4-methyl-6-tert-butylphenol), 2,2′-methylene-bis- (4-ethyl-6-tert-butylphenol), 4,4 '-Thiobis- (3-methyl-6-tert-butylphenol), 4,4'-butylidene-bis- (3-methyl-6-tert-butylphenol), 3,9-bis [{1,1-dimethyl- 2- {β- (3-tert-butyl-4-hydroxy-5-methylphenyl) propionyloxy} ethyl} 2,4,9,10-tetraoxaspiro] 5,5-undecane.

  Examples of the high molecular phenolic group include 1,1,3-tris- (2-methyl-4-hydroxy-5-tert-butylphenyl) butane, 1,3,5-trimethyl-2,4,6-tris (3 , 5-di-tert-butyl-4-bidoxybenzyl) benzene, tetrakis- {methylene-3- (3 ', 5'-di-tert-butyl-4'-hydroxyphenyl) propionate} methane, bis { (3,3'-bis-4'-hydroxy-3'-tert-butylphenyl) butyric acid} glycol ester, 1,3,5-tris (3 ', 5'-di-tert-butyl-4 '-Hydroxybenzyl) -s-triazine-2,4,6- (1H, 3H, 5H) trione, triphenol (vitamin E) and the like.

  Examples of sulfur-based compounds include dilauryl thiodipropionate, dimyristyl thiodipropionate, and distearyl thiopropionate.

  Examples of the phosphite system include triphenyl phosphite, diphenylisodecyl phosphite, phenyl diisodecyl phosphite, 4,4′-butylidene-bis (3-methyl-6-tert-butylphenyl-di-tridecyl) phosphite, Crick neopentanetetrayl bis (octadecyl phosphite), tris (mono and / or di) phenyl phosphite, diisodecyl pentaerythritol diphosphite, 9,10-dihydro-9-oxa-10-phosphaphenanthrene-10- Oxide, 10- (3,5-di-tert-butyl-4-hydroxybenzyl) -9,10-dihydro-9-oxa-10-phosphaphenanthrene-10-oxide, 10-decyloxy-9,10 -Dihydro-9-oxa-10-fo Phaphenanthrene, cyclic neopentanetetraylbis (2,4-di-tert-butylphenyl) phosphite, cyclic neopentanetetraylbis (2,6-di-tert-methylphenyl) phosphite, 2 , 2-methylenebis (4,6-tert-butylphenyl) octyl phosphite.

  In the present invention, phenol-based and phosphite-based antioxidants are preferably used in view of the effect of the antioxidant, thermal stability, economy, and the like, and it is more preferable to use both in combination. The addition amount of this antioxidant is about 0.1-1 mass% normally in the front surface protection sheet for solar cells, and it is preferable to add 0.2-0.5 mass%.

  As the ultraviolet absorber, various commercially available products can be applied, and various types such as benzophenone, benzotriazole, triazine, and salicylic acid ester can be exemplified. Examples of the benzophenone-based UV absorber include 2-hydroxy-4-methoxybenzophenone, 2-hydroxy-4-methoxy-2′-carboxybenzophenone, 2-hydroxy-4-octoxybenzophenone, 2-hydroxy-4-n. -Dodecyloxybenzophenone, 2-hydroxy-4-n-octadecyloxybenzophenone, 2-hydroxy-4-benzyloxybenzophenone, 2-hydroxy-4-methoxy-5-sulfobenzophenone, 2-hydroxy-5-chlorobenzophenone, 2, , 4-dihydroxybenzophenone, 2,2′-dihydroxy-4-methoxybenzophenone, 2,2′-dihydroxy-4,4′-dimethoxybenzophenone, 2,2 ′, 4,4′-tetrahydroxybenzophenone, etc. Can.

The benzotriazole ultraviolet absorber is a hydroxyphenyl-substituted benzotriazole compound, for example, 2- (2-hydroxy-5-methylphenyl) benzotriazole, 2- (2-hydroxy-5-t-butylphenyl) Benzotriazole, 2- (2-hydroxy-3,5-dimethylphenyl) benzotriazole, 2- (2-methyl-4-hydroxyphenyl) benzotriazole, 2- (2-hydroxy-3-methyl-5-t- Butylphenyl) benzotriazole, 2- (2-hydroxy-3,5-di-t-amylphenyl) benzotriazole, 2- (2-hydroxy-3,5-di-t-butylphenyl) benzotriazole, etc. be able to. Examples of triazine ultraviolet absorbers include 2- [4,6-bis (2,4-dimethylphenyl) -1,3,5-triazin-2-yl] -5- (octyloxy) phenol, 2- ( And 4,6-diphenyl-1,3,5-triazin-2-yl) -5- (hexyloxy) phenol. Examples of salicylic acid esters include phenyl salicylate and p-octylphenyl salicylate.
The addition amount of the ultraviolet absorber is usually about 0.01 to 2.0% by mass and preferably 0.05 to 0.5% by mass in the front protective sheet for solar cells.

  A hindered amine light stabilizer is suitably used as a weather stabilizer that imparts weather resistance in addition to the above ultraviolet absorber. A hindered amine light stabilizer does not absorb ultraviolet rays like an ultraviolet absorber, but exhibits a remarkable synergistic effect when used together with an ultraviolet absorber.

  Examples of hindered amine light stabilizers include dimethyl succinate-1- (2-hydroxyethyl) -4-hydroxy-2,2,6,6-tetramethylpiperidine polycondensate, poly [{6- (1,1 , 3,3-tetramethylbutyl) amino-1,3,5-triazine-2,4-diyl} {(2,2,6,6-tetramethyl-4-piperidyl) imino} hexamethylene {{2, 2,6,6-tetramethyl-4-piperidyl} imino}], N, N′-bis (3-aminopropyl) ethylenediamine-2,4-bis [N-butyl-N- (1,2,2, 6,6-pentamethyl-4-piperidyl) amino] -6-chloro-1,3,5-triazine condensate, bis (2,2,6,6-tetramethyl-4-piperidyl) sebacate, 2- (3 , 5-Di-tert-4- Mud alkoxybenzylacetic) -2-n-butyl malonic acid bis (1,2,2,6,6-pentamethyl-4-piperidyl) and the like. The amount of the hindered amine light stabilizer added is usually about 0.01 to 0.5% by mass, preferably 0.05 to 0.3% by mass, in the front protective sheet for solar cells.

  As a film forming method of the weather resistant layer (A), moisture proof layer (B) and flexible layer (C) used in the present invention, known methods such as a single screw extruder, a multi screw extruder, a Banbury mixer, a kneader, etc. An extrusion casting method using a T die, a calendar method, etc., which has a melt mixing facility, can be adopted and is not particularly limited. In the present invention, however, the T die is used in terms of handling properties and productivity. An extrusion casting method using is preferably used. The molding temperature in the extrusion casting method using a T-die is appropriately adjusted depending on the flow characteristics and film forming properties of the resin composition to be used, but is generally 130 to 300 ° C, preferably 150 to 250 ° C. Various additives such as silane coupling agents, antioxidants, UV absorbers, and weathering stabilizers may be dry blended with the resin in advance and then supplied to the hopper. The master batch may be supplied after being prepared, or a master batch in which only the additive is previously concentrated in the resin may be prepared and supplied.

The thickness of the front protective sheet for solar cells of the present invention is not particularly limited, but is usually about 0.05 to 1 mm, preferably 0.1 to 0.7 mm.
The solar cell front protective sheet of the present invention is formed by removing the film-formed weatherable layer (A), moisture-proof layer (B) and flexible layer (C) at a temperature of 120 to 150 ° C. with a vacuum laminator according to a conventional method. Manufacture can be carried out by heat-pressure bonding with a gas time of 2 to 15 minutes, a press pressure of 0.5 to 1 atm and a press time of 8 to 45 minutes.
In the present invention, the front protective sheet of the present invention has the weather resistant layer (A) as its surface side and the moisture proof layer (B) as its inner surface side, that is, from the front surface (upper part), the weather resistant layer (A ), The flexible layer (C), and the moisture-proof layer (B). In the present invention, with such a configuration, it is possible to prevent the moisture-proof layer from deteriorating and achieve long-term high moisture resistance and weather resistance.
The example of the front protective sheet for a solar cell shown in FIG. 1 is obtained by laminating a weather-resistant layer 1 and a moisture-proof layer 2 via a flexible layer 3 and bonding them together.

  The front protective sheet for solar cells in the present invention preferably has high transparency, and the total light transmittance thereof blocks the type of solar cell to be applied, for example, an amorphous thin film silicon type or sunlight that reaches a solar electronic device. When applied to a non-existing part, it may not be considered as important, but it is preferably 84% or more and 85% or more in consideration of the photoelectric conversion efficiency of the solar cell and the handling property when overlapping various members. More preferably. The total light transmittance can be measured according to JIS K7105, as will be described later.

  Moreover, about the moisture-proof performance of the front protective sheet for solar cells, the structure of the front protective sheet, in particular, a flexible layer (C) in which flexibility, heat resistance, and transparency are well balanced is used for the moisture-proof layer (B). By providing on the outer side (front surface), deterioration of the moisture-proof layer can be prevented by securing the flexibility of the front protective sheet, and long-term high moisture resistance and weather resistance can be achieved. The moisture-proof performance should be evaluated according to the conditions of JIS Z0222 “Moisture permeability test method for moisture-proof packaging containers” and JIS Z0208 “Moisture permeability test method for moisture-proof packaging material amount (cup method)”. Can do.

<Solar cell module, solar cell manufacturing method>
In order to manufacture the solar cell module and / or solar cell of the present invention using such a front protective sheet for solar cells, the front protective sheet of the present invention is used instead of the glass plate of the conventional solar cell. What is necessary is just to produce by the method.

  A solar cell module can be manufactured by fixing the solar cell element together with the back sheet using the solar cell front protective sheet of the present invention. As such a solar cell module, various types can be exemplified, and preferably, the solar cell front protective sheet, the sealing material, the solar cell element, and the lower protective material of the present invention. The solar cell module produced by using the upper protective material (front protective sheet for solar cell of the present invention) / sealing material (sealing resin layer) / solar cell element / sealing material (specifically, Sealing resin layer) / lower protective material (see FIG. 2), sealing material and upper protective material (for the solar cell of the present invention) on the solar cell element formed on the inner peripheral surface of the lower protective material A solar cell element formed on the inner peripheral surface of the upper protective material (the front protective sheet for solar cells of the present invention), such as a fluororesin-based transparent protective material A solar cell element produced by sputtering, etc. And the like as constituted as to form a sealing material and a lower protective material on top of.

  As the solar cell element, for example, a single crystal silicon type, a polycrystalline silicon type, an amorphous silicon type, a gallium-arsenic, a copper-indium-selenium, a cadmium-tellurium, or the like III-V group or II-VI group compound semiconductor type, Examples include a dye sensitizing type and an organic thin film type.

  About each member which comprises the solar cell module produced using the front surface protection sheet for solar cells of this invention, although it does not specifically limit, As a sealing material, for example, an ethylene-vinyl acetate copolymer Can be mentioned. The sealing material is preferably subjected to surface treatment such as corona treatment on at least one surface thereof from the viewpoint of ensuring adhesion to the front protective sheet. The lower protective material is a single layer or multilayer sheet such as a metal or various thermoplastic resin layers, for example, a metal such as tin, aluminum or stainless steel, an inorganic material such as glass, a polyester, an inorganic vapor deposition polyester, a fluorine-containing resin. And a single-layer or multilayer protective material such as polyolefin. The surface of the upper and / or lower protective material can be subjected to a known surface treatment such as a primer treatment or a corona treatment in order to improve the adhesion to the sealing material or other members.

  The upper protective material (the front protective sheet for solar cell of the present invention) / sealant / solar cell element / encapsulant / lower part described above for the solar cell module produced using the front protective sheet for solar cell of the present invention A configuration having a protective material will be described as an example. As shown in FIG. 2, the solar cell front protective sheet 10, the sealing resin layer 12 </ b> A, the solar cell elements 14 </ b> A and 14 </ b> B, the sealing resin layer 12 </ b> B, and the back sheet 16 are laminated in order from the sunlight receiving side. Further, a junction box 18 (a terminal box for connecting wiring for taking out the electricity generated from the solar cell element) is bonded to the lower surface of the back sheet 16. The solar cell elements 14A and 14B are connected by a wiring 20 in order to conduct the generated current to the outside. The wiring 20 is taken out through a through hole (not shown) provided in the back sheet 16 and connected to the junction box 18.

  As a manufacturing method of the solar cell module, a known manufacturing method can be applied and is not particularly limited, but in general, the solar cell front protective sheet, the sealing resin layer, the solar cell element of the present invention, It has the process of laminating | stacking a sealing resin layer and a lower protective material in order, and the process of vacuum-sucking them and carrying out thermocompression bonding. Also, batch type manufacturing equipment, roll-to-roll type manufacturing equipment, and the like can be applied.

  The solar cell module produced using the solar cell front protective sheet of the present invention is a small solar cell represented by a mobile device, a large size installed on a roof or a roof, depending on the type and module shape of the applied solar cell. It can be applied to various uses such as solar cells, both indoors and outdoors.

  In the solar cell module and / or solar cell of the present invention, this solar cell protective sheet, encapsulant, power generation element, encapsulant, and back surface protective sheet are removed at a temperature of 120 to 150 ° C. with a vacuum laminator according to a conventional method. Manufacture can be easily carried out by heat-pressure bonding with an air time of 2 to 15 minutes, a press pressure of 0.5 to 1 atm, and a press time of 8 to 45 minutes.

  EXAMPLES Hereinafter, the present invention will be described more specifically with reference to examples. However, the present invention is not limited by these examples and comparative examples. In addition, the various measured values and evaluation about the sheet | seat displayed in this specification were performed as follows.

(Physical property measurement)
(1) Crystal melting peak temperature (Tm)
Using a differential scanning calorimeter manufactured by PerkinElmer, Inc., under the trade name “Pyris1 DSC”, according to JIS K7121, about 10 mg of the sample was heated from −40 ° C. to 200 ° C. at a heating rate of 10 ° C./min. After holding at 200 ° C. for 5 minutes, the temperature was lowered to −40 ° C. at a cooling rate of 10 ° C./min, and again from the thermogram measured when the temperature was raised to 200 ° C. at a heating rate of 10 ° C./min. Tm) (° C.) was determined.

(2) Heat of crystal melting (ΔHm)
Using a differential scanning calorimeter manufactured by PerkinElmer Co., Ltd., trade name “Pyris1 DSC”, according to JIS K7122, about 10 mg of the sample was heated from −40 ° C. to 200 ° C. at a heating rate of 10 ° C./min. After holding at 200 ° C. for 5 minutes, the temperature was lowered to −40 ° C. at a cooling rate of 10 ° C./min, and again from the thermogram measured when the temperature was raised to 200 ° C. at a heating rate of 10 ° C./min (ΔHm ) (J / g).

(3) Storage elastic modulus measurement Using a viscoelasticity measuring device manufactured by IT Measurement Co., Ltd., trade name “Viscoelasticity Spectrometer DVA-200”, a sample (4 mm long, 60 mm wide) was subjected to vibration frequency 10 Hz, strain 0. Measurement was made from -150 ° C to 150 ° C in the transverse direction at 1%, a heating rate of 3 ° C / minute, and a chuck spacing of 25 mm, and the storage modulus (E ') (MPa) at 20 ° C was determined from the obtained data. .

(4) Total light transmittance The weatherproof layer, each flexible layer, and the moisture-proof layer are stacked between two pieces of white plate glass (size: length 75 mm, width 25 mm) having a thickness of 3 mm, and 150 ° C. for 15 minutes using a vacuum press machine. A sample that was laminated and pressed under the above conditions was prepared, the total light transmittance was measured according to JIS K7105, the value was described, and the results evaluated according to the following criteria were also shown.
(◎) Total light transmittance is 90% or more (○) Total light transmittance is 85% or more and less than 90% (×) Total light transmittance is less than 85% or clearly cloudy (not measured) )

(5) Heat resistance A flexible layer is layered between two pieces of 3 mm thick white sheet glass (size: length 75 mm, width 25 mm), and a sample that is laminated and pressed using a vacuum press machine at 150 ° C. for 15 minutes is prepared. The sample was installed at an inclination of 60 degrees in a constant temperature bath at 100 ° C., the state after 500 hours was observed, and evaluated according to the following criteria.
(○) The glass did not deviate from the initial reference position (×) The glass deviated from the initial reference position or the sheet melted

(Component layer)
(1) Weatherproof layer The total light transmittance of this ETFE using 50 μETFE AFLEX 50N1250D manufactured by Asahi Glass Co., Ltd. was 95%.

(2) Moisture-proof layer Mitsubishi Plastics Tech Barrier Lx in which silica was deposited on a 12 μm polyethylene terephthalate resin film was used. The total light transmittance of this moisture barrier layer was 86%.

(3) Flexible layer 1
As ethylene-α-olefin random copolymer (C-1), ethylene-octene random copolymer (manufactured by Dow Chemical Co., Ltd., trade name: ENGAGE 8200, octene content: 7.3 mol%) (24% by mass), MFR: 5, Tm: 65 ° C., ΔHm: 53 J / g) (hereinafter abbreviated as α-1) and 95 parts by mass and an ethylene-α-olefin block copolymer (C-2) As an ethylene-octene block copolymer (manufactured by Dow Chemical Co., Ltd., trade name: INFUSE D9100.05, octene content: 12.8 mol% (37 mass%), MFR: 1, Tm 119 ° C., ΔHm: 38 J / g) (hereinafter abbreviated as β-1) at a ratio of 5 parts by mass, a set temperature using a 40 mmφ single screw extruder equipped with a T die. 00 was melt-kneaded at ° C., thickness to obtain a flexible layer 1 of 0.5mm by quenching casting at 20 ° C. of cast rolls.

(4) Flexible layer 2
In the preparation of the flexible layer 1, as shown in Table 1, the resin composition constituting the sheet is 80 parts by mass of (α-1) and an ethylene-octene block copolymer (manufactured by Dow Chemical Co., Ltd., trade name: Infuse D9507.15, Octene content: 16.4 mol% (44 mass%), MFR: 5, Tm: 123 ° C., ΔHm: 21 J / g) (hereinafter abbreviated as β-2) 20 mass parts A flexible layer 2 having a thickness of 0.5 mm was obtained in the same manner as the flexible layer 1 except that the resin composition was changed to

(5) Flexible layer 3
In the preparation of the flexible layer 1, as shown in Table 1, the resin composition constituting the sheet is represented by (α-1) is an ethylene-propylene-hexene ternary random copolymer (manufactured by Nippon Polyethylene Co., Ltd., trade name: Kernel KJ640T, propylene content: 7.4 mol% (10 wt%), hexene content: 4.4 mol% (10 wt%), MFR: 30, Tm: 53 ° C., ΔHm: 58 J / g The flexible layer 3 having a thickness of 0.5 mm was obtained in the same manner as the flexible layer 1 except that it was changed to (hereinafter abbreviated as α-2).

(6) Flexible layer 4
In the preparation of the flexible layer 1, as shown in Table 1, the resin composition constituting the sheet was changed to (α-1) 100 parts by mass, in the same manner as in Example 1, and the thickness was 0.5 mm. A flexible layer 4 was obtained.

(7) Flexible layer 5
In the preparation of the flexible layer 1, as shown in Table 1, the resin composition constituting the sheet is an ethylene-octene random copolymer (manufactured by Prime Polymer Co., Ltd.) which is a general-purpose crystalline polyethylene resin. , Trade name: Moretech 0238CN, Octene content: 1 mol% (4 mass%), MFR: 2.1, Tm: 121 ° C., ΔHm: 127 J / g (hereinafter abbreviated as P-1) Except for the above, a flexible layer 5 having a thickness of 0.5 mm was obtained in the same manner as the flexible layer 1.

(8) Flexible layer 6
In the preparation of the flexible layer 1, as shown in Table 1, the resin composition constituting the sheet was changed to 100 parts by mass of (P-1), and the thickness was 0.5 mm in the same manner as the flexible layer 1. A flexible layer 6 was obtained.

(9) Flexible layer 7
An EVA sealant 496 manufactured by Etimex was used. In addition, this EVA sealing material single-piece | unit was vacuum-laminated by the method shown in the following Example, Then, only EVA sealing material was taken out and the total light transmittance was measured by the said method.

(10) Flexible layer 8
Toyo Ink's urethane adhesive (PU) IS801 and curing agent CR001 were blended at a ratio of 10: 1 and applied to a silicone release PET film so that the solid content coating amount was 10 g / m ^2. Cured for days. Thereafter, only the adhesive layer was taken out and the total light transmittance was measured by the above method.

The results of measuring the thickness, composition, total light transmittance, heat resistance, and flexibility (storage elastic modulus) of each of the obtained flexible layers 1 to 8 are summarized in Table 1 below.

Example 1
The prepared weather-resistant layer, flexible layer 1 and moisture-proof layer were laminated by a conventional method using a vacuum laminator LM-30x30 manufactured by NPC Corporation at 150 ° C. for 15 minutes to prepare a front protective sheet 1. Then, the total light transmittance was measured by the method similar to the flexible layer shown above using the produced front surface protection sheet 1, and the result is shown in Table 2. Furthermore, when moisture resistance was measured by the following method, the value was 0.24 g / (m ² · day).

(Dampproof)
The test was carried out in accordance with the conditions of JIS Z0222 “Method of testing moisture permeability of moisture-proof packaging container” and JIS Z0208 “Method of testing moisture permeability of moisture-proof packaging material (cup method)”. That is, using two laminated films or laminates each having a moisture permeable area of 10.0 cm × 10.0 cm square, a bag was prepared in which about 20 g of anhydrous calcium chloride was put as a hygroscopic agent and the four sides were sealed. The sample is placed in a constant temperature and humidity device with a relative humidity of 90%, and a mass measurement (in units of 0.1 mg) is performed for up to 14 days as an indication that the increase in mass is almost constant at intervals of 48 hours or more.
Water vapor transmission rate (g / m2 / 24h) = (m / s) / t
m: Mass increase in the last two weighing intervals (g)
s; Moisture permeable area (m2)
t: Time of last two weighing intervals (h) / 24 (h)

Example 2
The weather resistant layer, flexible layer 2 and moisture-proof layer were laminated by vacuum lamination in the same manner as in Example 1 to produce the front protective sheet 2 and the total light transmittance was measured in the same manner. The results are shown in Table 2. Moreover, when moisture-proof property was measured like Example 1, the value was 0.24 g / (m < ² > * day).

Example 3
The weatherproof layer, the flexible layer 3 and the moisture-proof layer were laminated by vacuum lamination in the same manner as in Example 1 to produce the front protective sheet 3 and the total light transmittance was measured. The results are shown in Table 2. Moreover, when moisture-proof property was measured like Example 1, the value was 0.21 g / (m < ² > * day).

Comparative Example 1
The weather resistant layer, flexible layer 4 and moisture-proof layer were laminated by vacuum lamination in the same manner as in Example 1 to prepare the front protective sheet 4 and the total light transmittance was measured. The results are shown in Table 2.

Comparative Example 2
The weather resistant layer, flexible layer 5 and moisture-proof layer were laminated by vacuum lamination in the same manner as in Example 1 to prepare the front protective sheet 5 and the total light transmittance was measured. The results are shown in Table 2.

Comparative Example 3
The weather resistant layer, flexible layer 6 and moisture-proof layer were laminated by vacuum lamination in the same manner as in Example 1 to prepare the front protective sheet 6 and the total light transmittance was measured. The results are shown in Table 2.

Comparative Example 4
The weather resistant layer, the flexible layer 7 and the moisture-proof layer were laminated by vacuum lamination in the same manner as in Example 1 to produce a front protective sheet 7 and the total light transmittance was measured. The results are shown in Table 2.

Comparative Example 5
The weather resistant layer, the flexible layer 8 and the moisture-proof layer were laminated by vacuum lamination in the same manner as in Example 1 to produce the front protective sheet 8 and the total light transmittance was measured. The results are shown in Table 2.

以上のようにして得られた本発明の前面保護シートは、高防湿性と耐候性を兼備し、透明性にも優れるものであった。尚、表中の「ＥＴＦＥ」は、旭硝子製ＥＴＦＥを、「ＢＦ」は三菱樹脂製テックバリアＬＸを意味するものとする。

The front protective sheet of the present invention obtained as described above has both high moisture resistance and weather resistance and is excellent in transparency. In the table, “ETFE” means ETFE made by Asahi Glass and “BF” means Tech Barrier LX made by Mitsubishi Plastics.

As is apparent from Tables 1 and 2, the flexible layers 1 to 3 used in the front protective sheet of the present invention have a good balance between flexibility, heat resistance and transparency necessary for protecting the moisture-proof layer. As shown, it had a sufficient thickness. Therefore, the front protective sheets of Examples 1 to 3 produced using the flexible layers 1 to 3 have both high moisture resistance and weather resistance, and are excellent not only in transparency but also in the long term. It can withstand use under high temperature and inclined conditions, and can be protected from impact from falling objects.
On the other hand, the flexible layers 4 and 8 are inferior in heat resistance, and when used under high temperature / inclined conditions, it has been revealed that the flexible layers 4 and 8 are deviated from the reference value or the sheet is melted. Therefore, in the front protective sheets of Comparative Examples 1 and 5 produced using the flexible layers 4 and 8, the flexible layer cannot fulfill its role, and it is considered that the moisture-proof layer is not sufficiently protected. That is, it is not preferable as a material for a solar cell member that is expected to be used under high temperature and inclined conditions. Moreover, the soft layers 5-7 were inferior to a softness | flexibility (storage elastic modulus), and it was shown that protection of a moisture-proof layer is inadequate. Therefore, also in the front protective sheets of Comparative Examples 2 to 4 produced using the flexible layers 5 to 7, the flexible layer cannot fulfill its role, and it is considered that the moisture-proof layer is not sufficiently protected.

DESCRIPTION OF SYMBOLS 1 ... Weatherproof layer 2 ... Moisture proof layer 3 ... Flexible layer 10 ... Front surface protection sheet 12A, 12B ... Sealing resin layer 14A, 14B ... Solar cell element 16 ...・ Back sheet 18 ... Junction box 20 ... Wiring

Claims (8)

The weather-resistant layer (A) and the moisture-proof layer (B), the ethylene-α-olefin random copolymer (C-1) that satisfies the following condition (1) and the ethylene-α that satisfies the following condition (2): - olefin block copolymer (C-2) and Ri greens are laminated via a flexible layer (C) containing, in a the flexible layer (C), the ethylene -α- olefin random copolymer (C the content of -1) is 50 to 99 wt%, for a solar cell content of the ethylene -α- olefin block copolymer (C-2) is characterized by 1-50% by mass Rukoto Front protective sheet.
(1) The heat of crystal fusion measured at a heating rate of 10 ° C./min in differential scanning calorimetry is 0 to 70 J / g.
(2) The crystal melting peak temperature measured at a heating rate of 10 ° C./min in differential scanning calorimetry is 100 ° C. or higher, and the crystal melting heat amount is 5 to 70 J / g.   The α-olefin in the ethylene-α-olefin block copolymer (C-2) is at least one selected from the group consisting of propylene, 1-butene, 1-hexene and 1-octene. Front protective sheet for solar cells.   The front protective sheet for solar cells according to claim 1 or 2, wherein the moisture-proof layer (B) has an inorganic oxide coating film on at least one surface of the base material layer.   The solar cell front protective sheet according to claim 3, wherein the base material layer has at least one resin selected from polyester, polyamide, and polyolefin.   The weathering layer (A) is a film in which a resin composition containing an ultraviolet absorber is formed on at least one resin selected from acrylic, polycarbonate, polyethylene terephthalate (PET), and polyethylene naphthalate (PEN), or fluorine It is a system resin layer, The front protective sheet for solar cells in any one of Claims 1-4.   The type of α-olefin constituting the ethylene-α-olefin random copolymer (C-1) and the ethylene-α-olefin block copolymer (C-2) is the same. A front protective sheet for a solar cell according to claim 1. The solar cell module produced using the front protective sheet for solar cells in any one of Claims 1-6 . The solar cell produced using the solar cell front surface protection sheet in any one of Claims 1-6 , or the solar cell module of Claim 7 .

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