Multilayer structure with adhesive properties

Abstract

The invention relates to a multilayer structure comprising an adhesive layer and in direct contact therewith, a layer forming a support film, wherein said adhesive layer comprises a polyolefin A and a functionalized polyolefin and has a melting point of between 80°C and 120°C, and wherein said support film comprises a polyamide-grafted polymer and has a flow temperature higher than 160°C. It also relates to a method for the manufacture thereof, to the use of such a multilayer structure for the manufacture of photovoltaic modules and to a method for manufacturing such modules and also to these photovoltaic modules as such.

Description

[0001] Description

[0002] Title: Multilayer structure with adhesive properties

[0003] Field of Invention

[0004] The invention relates to a multilayer structure, in particular a bilayer structure, useful in particular as an encapsulant for photovoltaic modules. It also relates to photovoltaic modules comprising such a multilayer structure.

[0005] Technical background

[0006] Global warming, linked to greenhouse gases released by fossil fuels, further reinforces the interest in alternative energy solutions that do not emit such gases during their operation, such as photovoltaic modules.

[0007] There are many types of photovoltaic module structures. Figure 1 shows a typical photovoltaic cell; a photovoltaic cell (10) comprises cells (12), one cell containing a photovoltaic sensor (14) in contact with electron collectors (16) placed above (upper collectors) and below (lower collectors) the photovoltaic sensor. The upper collectors (16) of one cell are connected to the lower collectors (16) of another cell (12) by conductive bars (18), also called electrical interconnectors, generally made of a metal alloy. In other embodiments, the interconnectors are all located on the same side of the cells. All these cells (12) are connected together, in series and / or in parallel, to form the photovoltaic cell (10).When the photovoltaic cell (10) is placed under a light source, it delivers a direct electric current, which can be recovered at the terminals (19) of the cell (10).

[0008] Figure 2 shows a photovoltaic module (20) comprising the photovoltaic cell (10) of Figure 1 coated with an encapsulant (22) composed of an upper part and a lower part. The encapsulated cell is further protected by an upper protective layer (24) (called in English "frontsheet") and a protective layer on the back of the module (called in English "backsheet") (26). The upper protective layer (24), generally made of glass, provides protection against shock and humidity of the photovoltaic cell. The protective layer on the back of the module (26), generally made of thermoplastic or crosslinkable resin, also contributes to its protection against humidity and furthermore to the electrical insulation of the cells by avoiding any contact with the external environment.

[0009] To ensure effective protection, it is important that the encapsulant perfectly fills the space between the photovoltaic cell and the protective layers. In addition, its adhesion to the protective layers must be perfect and durable, even at temperatures of 80°C or more, which can be reached under solar radiation.

[0010] To promote adhesion, either "chemical" techniques can be used, using a specific binder or adhesion promoter, or physical techniques such as corona or plasma surface treatment. However, these methods require additional operations that are sometimes complex, often resulting in disappointing results, and are costly. In addition, physical surface treatments are not stable over time and require careful storage and handling precautions.

[0011] Currently, to manufacture a photovoltaic module, the front sheet, the encapsulant, the battery and the back sheet are assembled simultaneously, most often using a vacuum lamination process. The encapsulant is melted during the lamination step to coat the active layers of the battery.

[0012] In addition to handling numerous films, this lamination assembly process has disadvantages related to the shrinkage of the encapsulant film, which can reach 10%, or sometimes even 50%. This shrinkage can lead to defects in the photovoltaic module such as air bubbles, creases, blisters, edge coverage defects or breaks in the connectors between cells. All of these defects cause rejects or can reduce the lifespan and efficiency of photovoltaic modules.

[0013] To limit these problems, the encapsulant film can be produced by an extrusion process followed by a post-annealing step, but this reduces the extrusion speed and therefore increases its cost. Application EP 2 673 809 A1 discloses a bilayer film composed of a backsheet and an encapsulant making it possible to overcome at least some of these problems. However, the implementation of these bilayer structures requires successively stacking a first layer of encapsulant, the photovoltaic module, a second layer of encapsulant and finally a layer forming the backsheet, as shown in Figure 2. In addition to a first layer of encapsulant 400 μm thick, bilayer structures 800 μm thick are thus described. The significant thickness of these structures adds significant weight and cost.Furthermore, the encapsulant does not provide sufficient adhesion to the metal to be able to be used in processes comprising a prior rolling step on the surface of the metal interconnectors.

[0014] Furthermore, these bilayer films cannot be used for the preparation of photovoltaic modules having certain geometric configurations, in particular connections located on the same side as the photovoltaic sensors, such as those described for example in application WO 2004 / 021455, and which require laminating the encapsulant directly to the surface of the interconnectors.

[0015] There is therefore a need to have multilayer structures, particularly for photovoltaic modules, which make it possible to overcome the drawbacks of the state of the art, in particular to improve the productivity of the preparation processes and the quality of the photovoltaic modules and which are versatile and therefore compatible with different geometric configurations and assembly processes of photovoltaic modules.

[0016] Summary of the invention

[0017] The present invention seeks to overcome the problems encountered in the prior art by providing a multilayer structure, in particular a two-layer structure, comprising an adhesive layer and a support film. In its broadest definition, the invention relates to a multilayer structure comprising an adhesive layer which can serve as an encapsulant and a support film which can serve as a backsheet, characterized in that the adhesive layer comprises a polyolefin A and a functional polyolefin and has a specific melting point in that the support film has a specific flow temperature.

[0018] Indeed, it was found that by combining a polyolefin A with a functional polyolefin in the adhesive layer, it was possible to obtain a multilayer structure exhibiting both very good thermal stability and excellent adhesion with the metal of the electrical interconnectors of photovoltaic cells.

[0019] The improved adhesion of the multilayer structure to the interconnectors has a dual advantage. On the one hand, it facilitates the assembly process, particularly by avoiding prior surface treatments. On the other hand, it ensures reliable electrical contact between the interconnectors and the photovoltaic cells, thus giving the photovoltaic modules greater efficiency and a longer service life.

[0020] Finally, the multilayer structures of the invention can be of low thickness, in particular less than 100 μm.

[0021] The multilayer structures according to the invention thus allow the manufacture of photovoltaic modules that are both of better quality and less expensive.

[0022] Thus, the present invention relates to a multilayer structure comprising an adhesive layer and a layer forming a support film in direct contact therewith, wherein

[0023] (a) said adhesive layer comprises:

[0024] - a polyolefin A chosen from a homopolymer of ethylene and a copolymer of ethylene and an α-olefin, a copolymer of ethylene and a vinyl ester of carboxylic acid, in particular a vinyl acetate (EVA) or a (co)polymer comprising methyl, ethyl, propyl, n-butyl, sec-butyl, isobutyl or tert-butyl (meth)acrylate units; and

[0025] - a functionalized polyolefin, distinct from polyolefin A, comprising a polyolefin backbone containing a residue of at least one unsaturated monomer (Y), the residue of the unsaturated monomer (Y) being fixed to the backbone by grafting or copolymerization; the melting temperature of the adhesive layer being between 80°C and 120°C, b) Said support film comprises a polyamide grafted polymer comprising:

[0026] - a polyolefin backbone, representing from 50% to 95% by mass of the polyamide graft polymer, containing a remainder of at least one unsaturated monomer (X) and at least one polyamide graft, representing from 5% to 50% by mass of said polyamide graft polymer, wherein: o The polyamide graft is attached to the polyolefin backbone by the remainder of the unsaturated monomer (X) comprising a function capable of reacting by a condensation reaction with a polyamide having at least one amine end and / or at least one carboxylic acid end, o The remainder of the unsaturated monomer (X) is attached to the backbone by grafting or copolymerization, o The polyolefin backbone and the polyamide graft being chosen so that said polyamide graft polymer has a flow temperature above 160°C, as measured by DSC according to ISO 11357-1:2016, ISO 11357-2:2020, ISO 11357-3:2018,said flow temperature being defined as the highest temperature among the melting temperatures and the glass transition temperatures of the polyamide graft and the polyolefin backbone.,

[0027] Other advantageous features of the invention are:

[0028] - the melting temperature of said adhesive layer is between 90°C and 110°C.

[0029] - said adhesive layer has a Melt Flow Index (MFI), as measured according to ASTP D 1238 at 190°C under 2.16 kg, of between 0.2 and 10 g / 10 min, preferably between 0.4 and 3 g / 10 min, and in particular between 0.6 and 2 g / 10 min.

[0030] - said adhesive layer comprises: o from 65% to 95% by weight of polyolefin A; o from 5 to 35% by weight of functional polyolefin; and o from 0 to 5% by weight of one or more additives. - The thickness of said adhesive layer is between 20 and 60 μm.

[0031] - The thickness of said support film is between 5 and 40 pm.

[0032] - The α-olefin comonomer of the polyolefin A of the adhesive layer is selected from ethylene-propylene, ethylene-butene and ethylene-octene.

[0033] - The functional polyolefin of the adhesive layer is a polyolefin containing a residue of at least one unsaturated monomer (Y) which is a maleic anhydride.

[0034] - Said support film has a Melt Flow Index (MFI), as measured according to ASTP D 1238 at 230°C under 2.16 kg, of between 0.2 and 10 g / 10 min, preferably between 0.4 and 3 g / 10 min, in particular between 0.6 and 2 g / 10 min.

[0035] - Said support film carries Said adhesive layer on one of its faces.

[0036] - Said support film carries Said adhesive layer on both sides.

[0037] - Said support film is assembled to Said adhesive layer by coextrusion.

[0038] According to another aspect, the invention aims at the use of such a multilayer structure for the manufacture of photovoltaic modules.

[0039] According to yet another aspect, the invention relates to a method for preparing a photovoltaic module, in which a photovoltaic cell is encapsulated with such a multilayer structure.

[0040] In this process, encapsulation may include the steps of:

[0041] (i) attaching an electrically conductive filament to the surface of said adhesive layer of such a multilayer structure at a temperature below the melting temperature of said adhesive layer to form an assembly;

[0042] (ii) bringing said assembly into contact with a photovoltaic cell at a temperature between the melting temperature of the adhesive layer and the flow temperature of the support film.

[0043] According to a final aspect, the invention relates to a photovoltaic module comprising such a multilayer structure. Description of the Figures

[0044] The following description is given solely for illustrative and non-limiting purposes with reference to the appended figures, in which: Figure 1 represents an example of a photovoltaic cell, parts (a) and (b) being % views, part (a) showing a cell before connection and part (b) a view after connection of 2 cells; part (c) is a top view of a complete photovoltaic cell; and Figure 2 represents a cross-section of a photovoltaic module, the “conventional” photovoltaic sensor of which is encapsulated by an upper encapsulant film and a lower encapsulant film.

[0045] Description of the invention

[0046] Thus, according to a first aspect, the invention relates to a multilayer structure, in particular as an encapsulant for a photovoltaic cell, comprising an adhesive layer and a layer forming a support film in direct contact therewith, wherein the adhesive layer comprises a polyolefin A and a functionalized polyolefin, the melting temperature of the adhesive layer being between 80°C and 120°C, and wherein the support film comprises a specific polyamide graft polymer having a flow temperature above 160°C, as measured by DSC according to ISO 11357-1:2016, ISO 11357-2:2020, ISO 11357-3:2018, the flow temperature being defined as the highest temperature among the melting temperatures and the glass transition temperatures of the polyamide graft and the polyolefin backbone.

[0047] A. Multi-layer structure

[0048] According to the invention, the adhesive layer of the multilayer structure is in direct contact with the support film.

[0049] In the absence of additional layers, the multilayer structure may form a two-layer structure. However, it may also comprise other layers, in principle any. According to a preferred embodiment, the multilayer structure may be a three-layer structure, and in particular comprise a support film provided with an adhesive layer as defined below on its two faces.

[0050] A.1. Adhesive layer

[0051] According to the invention, the adhesive layer of the multilayer structure comprises a specific polyolefin A and a separate functional polyolefin, the melting temperature of the adhesive layer being between 80°C and 120°C. The polyolefins will be described in more detail below.

[0052] Polyolefin A

[0053] The polyolefin A present in the adhesive layer may be a homopolymer of ethylene or a copolymer of ethylene with a comonomer selected from an α-olefin, an alkyl (meth)acrylate or a vinyl ester of a carboxylic acid, in particular a vinyl acetate. In the copolymer, the α-olefin may have 3 to 30, in particular 3 to 8, carbon atoms. Examples of α-olefins include propylene, 1-butene, 1-pentene, 3-methyl-1-butene, 1-hexene, 4-methyl-1-pentene, 3-methyl-1-pentene, 1-octene, 1-decene, 1-dodecene, 1-tetradecene, 1-hexadecene, 1-octadecene, 1-eicocene, 1-dococene, 1-tetracocene, 1-hexacocene, 1-octacocene, and 1-triacontene. These α-olefins may be used alone or in a mixture of two or more.

[0054] Preferably, the ethylene-α-olefin copolymers comprise a mass content of ethylene greater than 50%.

[0055] Ethylene-α-olefin copolymers are obtained by methods known to those skilled in the art, such as Ziegler-Natta, metallocene or organometallic polymerization described for example in WO 2008 / 036707.

[0056] Particularly preferred as polyolefin A is a polyethylene, especially linear low density polyethylene (LLDPE), or a copolymer of ethylene with a single α-olefin, selected from ethylene-propylene, ethylene-butene and ethylene octene.

[0057] According to another embodiment, polyolefin A is a copolymer of ethylene and alkyl (meth)acrylate, the term alkyl (meth)acrylate grouping together alkyl acrylates or methacrylates. The alkyl chains of these (meth)acrylates can have up to 30 carbon atoms. Examples of alkyl chains that may be mentioned are methyl, ethyl, propyl, n-butyl, sec-butyl, lsobutyl, tert-butyl, pentyl, hexyl, heptyl, octyl, 2-ethylhexyl, nonyl, decyl, undecyl, dodecyl, tridecyl, tetradecyl, pentadecyl, hexadecyl, heptadecyl, octadecyl, nonadecyl, eicosyl, hencosyl, docosyl, tricosyl, tetracosyl, pentacosyl, hexacosyl, heptacosyl, octacosyl, nonacosyl. Methyl, ethyl and butyl (meth)acrylates are preferred.

[0058] Ethylene-alkyl (meth)acrylate copolymers are conventionally obtained by processes known to those skilled in the art, such as, for example, the high-pressure autoclave or tubular process.

[0059] According to a particularly preferred embodiment, polyolefin A is a copolymer of ethylene and vinyl acetate (EVA).

[0060] Preferably, polyolefin A has a melting temperature of between 90°C and 110°C, and in particular between 90°C and 105°C.

[0061] According to one embodiment, the enthalpy of fusion of polyolefin A is less than 130 J / g, and in particular between 80 and 120 J / g (2 ème DSC heating according to ISO 11347 at 40°C / min).

[0062] The density of polyolefin A, measured according to ASTM D 1505, is preferably 0.860 to 0.960, particularly 0.860 to 0.920.

[0063] Indeed, without wishing to limit itself to a particular theory, the applicant was able to observe that a low enthalpy of fusion, included in the interval mentioned above, reflecting a low crystallinity rate, made it possible to favorably influence the adhesion of the adhesive layer to the metal.

[0064] Functional polyolefin

[0065] The term “functional polyolefin” is understood to mean, within the meaning of the present description, a polyolefin distinct from polyolefin A present in the adhesive layer and comprising reactive functions, and capable of reacting on contact with a metal surface.

[0066] Such reactive functions include epoxide, carboxylic acid, carboxylic acid anhydride, carboxylic acid amide and carboxylic acid ester functions.

[0067] The functionalized polyolefin present in the adhesive layer comprises a polyolefin backbone containing a residue of at least one unsaturated monomer (Y) selected from an unsaturated epoxide, an unsaturated carboxylic acid anhydride, an unsaturated carboxylic acid, or a salt thereof, the remainder of the unsaturated monomer (Y) being attached to the backbone by grafting or copolymerization.

[0068] These functions promote interaction with the metal surface in contact with the electrical interconnectors, which improves the adhesion between the multilayer structure and the electrical interconnectors.

[0069] Functional polyolefins may in particular be derived from monomers such as meth(acrylic acid), (meth)acrylamide or vinyl acetate. According to one embodiment, the polyolefin backbone of the functional polyolefin is a polyethylene backbone, in particular a homopolymer or a copolymer of ethylene.

[0070] The unsaturated monomer (Y) may be an unsaturated epoxide, in particular chosen from aliphatic glycidyl esters and ethers such as allyl glycidyl ether, vinyl glycidyl ether, glycidyl maleate and itaconate, glycidyl acrylate and methacrylate; alicyclic glycidyl esters and ethers such as 2-cyclohexene-1-glycidyl ether, cyclohexene-4,5-diglycidylcarboxylate, cyclohexene-4-glycidyl carboxylate, 5-norbornene-2-methyl-2-glycidyl carboxylate and endocis-bicyclo(2,2,1)-5-heptene-2,3-diglycidyl dicarboxylate, glycidyl methacrylate being preferred.

[0071] Alternatively, the unsaturated monomer (Y) may be an unsaturated carboxylic acid or a salt thereof, including acrylic acid or methacrylic acid and their salts.

[0072] Alternatively, the unsaturated monomer (Y) may be an unsaturated carboxylic acid ester, in particular an alkyl (meth)acrylate, the term alkyl (meth)acrylate grouping together alkyl acrylates or methacrylates. The alkyl chains of these (meth)acrylates may have up to 30, in particular up to 24, carbon atoms. Examples of alkyl chains include methyl, ethyl, propyl, n-butyl, sec-butyl, isobutyl, tert-butyl, pentyl, hexyl, heptyl, octyl, 2-ethylhexyl, nonyl, decyl, undecyl, dodecyl, tridecyl, tetradecyl, pentadecyl, hexadecyl, heptadecyl, octadecyl, nonadecyl, eicosyl, hencosyl, docosyl, tricosyl, tetracosyl, pentacosyl, hexacosyl, heptacosyl, octacosyl, and nonacosyl, in particular methyl, ethyl, and butyl (meth)acrylates.

[0073] Alternatively, the unsaturated monomer (Y) may be a carboxylic acid anhydride, in particular selected from maleic, itaconic, citraconic, alkylsuccinic, cycLohex-4-ene-1,2-dicarboxylic, 4-methylenecycLohex-4-ene-1,2-dicarboxylic, bicyclo(2,2,1)hept-5-ene-2,3-dicarboxylic, and x-methylbicycLo(2,2,1)hept-5-ene-2,2-dicarboxylic anhydrides. Among these, maleic anhydride is preferred.

[0074] The unsaturated monomer (Y) can also be a vinyl ester of a carboxylic acid, in particular a vinyl acetate.

[0075] Alternatively, the unsaturated monomer (Y) may also be a (meth)acrylamide, selected from acrylamide and methacrylamide.

[0076] The unsaturated monomer (Y) in the functional polyolefin is attached by grafting or copolymerization.

[0077] Preferably, the functional polyolefin does not comprise a polyamide graft.

[0078] Preferably, the functional polyolefin is an ethylene copolymer containing an unsaturated carboxylic acid anhydride residue, especially maleic anhydride.

[0079] The ethylene copolymer may be a copolymer of ethylene and a comonomer chosen from unsaturated carboxylic acid esters such as, for example, alkyl acrylates or alkyl methacrylates grouped under the term alkyl (meth)acrylates as specified above.

[0080] Copolymers of ethylene and unsaturated carboxylic acid esters can be obtained by processes known to those skilled in the art, such as, for example, the high-pressure autoclave or tubular process.

[0081] According to a preferred embodiment, the functional polyolefin is an ethylene-alkyl (meth)acrylate-maleic anhydride terpolymer.

[0082] According to one embodiment, the adhesive layer comprises at least 65% by weight of a polyolefin A as defined above.

[0083] According to another embodiment, the adhesive layer comprises at least 5% by weight of a functional polyolefin.

[0084] According to a preferred embodiment, the adhesive layer comprises: from 65% to 95% by weight of a polyolefin A as defined above; from 5 to 30% by weight of a functional polyolefin; as well as from 0 to 5% by weight of additives, in particular chosen from plasticizers, adhesion promoters, UV stabilizers, UV absorbers, antioxidants, and pigments.

[0085] Plasticizers may be added to the adhesive layer in order to facilitate implementation and improve the productivity of the manufacturing process for multilayer structures and / or photovoltaic modules. Examples include aromatic or naphthalenic paraffinic mineral oils which also improve the adhesive power of the structures according to the invention. Other plasticizers that may be mentioned are phthalates, azelates, adipates and ticresyl phosphate.

[0086] Coloring or brightening compounds can also be added.

[0087] Similarly, adhesion promoters, although not necessary, may be advantageously added to further improve the adhesive power of the structure. The adhesion promoter is a non-polymeric ingredient; it may be organic, crystalline, inorganic and more preferably semi-organic semi-mineral. These include organic titanates or silanes, such as monoalkyl titanates, trichlorosilanes and trialkoxysilanes.

[0088] Advantageously, trialcooxysilanes containing an epoxy, vinyl or amine group will be used, in particular when these adhesion promoters are added in the form of a master batch. It may also be provided that these adhesion promoters are diluted or mixed with the functional or non-functional polyolefin of the adhesive layer by a technique well known to those skilled in the art, for example compounding.

[0089] Since UV radiation may cause slight yellowing of the adhesive layer, UV stabilizers and UV absorbers such as benzotriazole, benzophenone and other hindered amines may be added to the adhesive layer and / or the carrier film in order to prolong the transparency of the multilayer structure and thus its lifetime.

[0090] The adhesive layer may further comprise 0 to 5% by weight, in particular 0.1 to 4.5%, in particular 0.5 to 4%, and very particularly 1 to 3% by weight of one or more of these additives, relative to the total weight of the composition.

[0091] The adhesive layer may further comprise one or more antioxidants to limit yellowing during the manufacture of the adhesive layer. Preferred antioxidants are, for example, phosphorus compounds (phosphonites and / or phosphites) and hindered phenolics.

[0092] The adhesive layer may in particular comprise 0 to 3% by weight, in particular 0.1 to 2.5%, in particular 0.5 to 2%, and very particularly 1 to 1.5% by weight of one or more antioxidants relative to the total weight of the composition.

[0093] Pigments such as coloring or brightening compounds can also be added to the adhesive layer in proportions generally ranging from 0.01 to 2% relative to the total mass of the composition.

[0094] According to one embodiment, the thickness of the adhesive layer is between 20 and 60 μm.

[0095] The melting temperature of the adhesive layer is preferably between 80 and 110°C, preferably between 90°C and 100°C.

[0096] Indeed, the inventors were able to observe that if the melting temperature is lower, the multilayer structure can be difficult to handle, in particular during the coextrusion step with the support film and / or during its subsequent use, in particular during the rolling step on the surface of the filaments. Conversely, a melting temperature above 120°C is generally accompanied by a higher crystallinity rate which can reduce adhesion to the metal filaments.

[0097] According to one embodiment, the adhesive layer has a melt flow index (MFI) of between 0.2 and 10 g / 10 min, preferably between 0.4 and 3 g / 10 min, and more preferably between 0.6 and 2 g / 10 min, measured according to standard ASTM D1238 at 190°C / 2.16 kg.

[0098] A.2. Support film

[0099] The support film comprises a polyamide graft polymer comprising a polyolefin backbone containing a residue of at least one unsaturated monomer (X) and at least one polyamide graft, the polyamide graft being attached to the polyolefin backbone by the residue of the unsaturated monomer (X) comprising a function capable of reacting by a condensation reaction with a polyamide, the polyolefin backbone and the polyamide graft being chosen so that said polyamide graft polymer has a flow temperature greater than 160°C.

[0100] The flow temperature of the polyamide graft polymer is defined as the higher of the melting temperatures and glass transition temperatures of the polyamide grafts and the polyolefin backbone. The backbone and grafts are selected so that the flow temperature of the polyamide graft polymer is greater than 160°C.

[0101] The polyamide graft polymer comprises 50 to 95%, preferably 60 to 90% and in particular 70 to 85% by mass of a polyolefin backbone containing a residue of at least one unsaturated monomer (X).

[0102] With regard to the polyolefin backbone, it is preferably a polymer comprising as monomer an α-olefin, in particular comprising 2 to 30 carbon atoms.

[0103] Examples of α-olefins include ethylene, propylene, 1-butene, 1-pentene, 3-methyl-1-butene, 1-hexene, 4-methyl-1-pentene, 3-methyl-1-pentene, 1-octene, 1-decene, 1-dodecene, 1-tetradecene, 1-hexadecene, 1-octadecene, 1-eicocene, 1-dococene, 1-tetracocene, 1-hexacocene, 1-octacocene, and 1-triacontene.

[0104] Mention may also be made of cycloolefins having 3 to 30, in particular 3 to 20 carbon atoms, such as cyclopentane, cycloheptene, norbornene, 5-methyl-2-norbornene, tetracyclododecene, and 2-methyl-1,4,5,8-dimethano-1,2,3,4,4a,5,8,8a-octahydronaphthalene; di- and polyolefins, such as butadiene, isoprene, 4-methyl-1,3-pentadiene, 1,4-pentadiene, 1,5-hexadiene, 1,3-hexadiene, 1,3-octadiene, 1,4-octadiene, 1,5-octadiene, 1,6-octadiene, ethylidenenorbornene, vinyl norbornene, dicyclopentadiene, 7-methyl-1,6-octadiene, 4-ethylidiene-8-methyl-1,7-nonadiene, and 5,9-dimethyl-1,4,8-decatriene;aromatic vinyl compounds such as mono- or polyalkylstyrenes (including styrene, o-methylstyrene, m-methylstyrene, p-methylstyrene, o,p-dimethylstyrene, o-ethylstyrene, m-ethylstyrene and p-ethylstyrene), and derivatives comprising functional groups such as methoxystyrene, ethoxystyrene, vinyl benzoic acid, methyl vinyl benzoate, benzyl vinyl acetate, hydroxystyrene, o-chlorostyrene, p-chlorostyrene, di-vinyl benzene, 3-phenylpropene, 4-phenylpropene, a-methylstyrene, vinyl chloride, 1,2-difluoroethylene, 1,2-dichloroethylene, tetrafluoroethylene, and 3,3,3-trifluoro-1-propene, propylene and ethylene being preferred.;

[0105] The polyolefin may be a homopolymer when only one α-olefin is polymerized. Examples include polyethylene (PE) or polypropylene (PP). It may also be a copolymer when at least two comonomers are copolymerized in the polymer chain, the first of the at least two monomers being an α-olefin and the other comonomers being a monomer capable of polymerizing with the first monomer.

[0106] Other comonomers include:

[0107] - one of the α-olefins already mentioned above, different from the first α-olefin comonomer;

[0108] - dienes such as, for example, 1,4-hexadiene, ethylidene, norbornene, butadiene;

[0109] - esters of unsaturated carboxylic acids such as alkyl acrylates or alkyl methacrylates grouped under the term alkyl (meth)acrylates. The alkyl chains of these (meth)acrylates can have up to 30 carbon atoms. Alkyl chains that may be mentioned are methyl, ethyl, propyl, n-butyl, sec-butyl, Isobutyl, tert-butyl, pentyl, hexyl, heptyl, octyl, 2-ethylhexyl, nonyl, decyl, undecyl, dodecyl, tridecyl, tetradecyl, pentadecyl, hexadecyl, heptadecyl, octadecyl, nonadecyl, eicosyl, hencosyl, docosyl, tricosyl, tetracosyl, pentacosyl, hexacosyl, heptacosyl, octacosyl, nonacosyl, methyl, ethyl and butyl (meth)acrylates being preferred; and

[0110] - vinyl esters of carboxylic acids. Examples of vinyl esters of carboxylic acids include vinyl acetate, vinyl versatate, vinyl propionate, vinyl butyrate, or vinyl maleate, with vinyl acetate being preferred.

[0111] Advantageously, the polyolefin backbone consists of at least 50 mol% of the first comonomer. Preferred polyolefin backbones consist of ethylene-alkyl (meth)acrylate copolymer. By using this polyolefin backbone, excellent resistance to aging in light and temperature is obtained.

[0112] According to the present invention, the polyolefin backbone contains at least one unsaturated monomer residue (X) capable of reacting with an acid and / or amine function of the polyamide graft by a condensation reaction. It is specified that this unsaturated monomer (X) is not a “second comonomer”.

[0113] As unsaturated monomer (X), we can cite:

[0114] - unsaturated epoxides. Among these, aliphatic glycidyl esters and ethers such as allyl glycidyl ether, vinyl glycidyl ether, glycidyl maleate and itaconate, glycidyl acrylate and methacrylate; alicyclic glycidyl esters and ethers such as 2-cyclohexene-1-glycidyl ether, cyclohexene-4,5-diglycidylcarboxylate, cyclohexene-4-glycidyl carboxylate, 5-norbornene-2-methyl-2-glycidyl carboxylate and endocis-bicyclo(2,2,1)-5-heptene-2,3-diglycidyl dicarboxylate, with glycidyl methacrylate being preferred.

[0115] - unsaturated carboxylic acids and their salts, for example acrylic acid or methacrylic acid and their salts.

[0116] - carboxylic acid anhydrides, chosen for example from maleic, itaconic, citraconic, allylsuccinic, cyclohex-4-ene-1,2-dicarboxylic, 4-methylenecyclohex-4-ene-1,2-dicarboxylic, bicyclo(2,2,1)hept-5-ene-2,3-dicarboxylic, and x-methylbicyclo(2,2,1)hept-5-ene-2,2-dicarboxylic anhydrides, in particular maleic anhydride.

[0117] The unsaturated monomer (X) is preferably chosen from an unsaturated carboxylic acid anhydride and an unsaturated epoxide. In particular, to carry out the condensation of the polyamide graft with the polyolefin backbone, in the case where the reactive end of the polyamide graft is a carboxylic acid function, the unsaturated monomer (X) is preferably an unsaturated epoxide. In the case where the reactive end of the polyamide graft is an amine function, the unsaturated monomer (X) is advantageously an unsaturated epoxide and preferably an unsaturated carboxylic acid anhydride. According to an advantageous version of the invention, the preferred number of unsaturated monomer (X) attached on average to the polyolefin backbone is greater than or equal to 1.3 and / or preferably less than or equal to 10.Thus, if (X) is maleic anhydride and the number-average molar mass of the polyolefin is 15,000 g / mol, this has been found to correspond to a proportion of anhydride of at least 0.8% by mass of the entire polyolefin backbone and at most 6.5%. These values, together with the mass of the polyamide grafts, determine the proportion of polyamide and backbone in the polyamide graft polymer.

[0118] The polyolefin backbone containing the remainder of the unsaturated monomer (X) is obtained by polymerization of the monomers (first comonomer, optional second comonomer, and optionally unsaturated monomer (X)). This polymerization can be carried out by a high-pressure radical process or a solution process, in an autoclave or tubular reactor, these processes and reactors being well known to those skilled in the art. When the unsaturated monomer (X) is not copolymerized in the polyolefin backbone, it is grafted onto the polyolefin backbone. Grafting is also an operation known per se. The composition would be in accordance with the invention if several different functional monomers (X) were copolymerized and / or grafted onto the polyolefin backbone.

[0119] Depending on the type and ratio of monomers, the polyolefin backbone can be semi-crystalline or amorphous. For amorphous polyolefins, only the glass transition temperature is observed, while for semi-crystalline polyolefins, a glass transition temperature and a melting temperature are observed. A polyolefin backbone with the desired glass transition and eventual melting temperature can be obtained by adjusting the type and ratio of monomers. The molar mass of the polyolefin backbone can be varied to obtain the desired viscosity.

[0120] The polyolefin trunk has a Melt Flow Index (MFI) preferably between 3 and 400g / 10min, in particular between 10 and 300g / 10 min and notably between 50 and 200g / 10 min (190°C, 2.16kg, ASTM D 1238).

[0121] Preferably, its density, as measured according to ISO 1183:2019, is advantageously between 0.91 and 0.96. The polyamide graft polymer comprises a polyolefin backbone containing a residue of at least one unsaturated monomer (X) as described above and at least one polyamide graft attached to the polyolefin backbone via the residue of the unsaturated monomer (X).

[0122] Polyamide grafts can be homopolyamides or copolyamides. Polyamide grafts can be aliphatic, cycloaliphatic or semiaromatic.

[0123] Among the homopolyamides, preferred are aliphatic polyamides which result from the polycondensation of: a lactam, an aliphatic α,γ-aminocarboxylic acid, or an aliphatic diamine and an aliphatic diacid.

[0124] Examples of lactams include caprolactam, oenantholactam, and lauryllactam.

[0125] Examples of aliphatic α,γ-aminocarboxylic acid include aminocaproic acid, 7-aminoheptanoic acid, 11-aminoundecanoic acid, and 12-aminododecanoic acid.

[0126] Examples of aliphatic diamines include hexamethylenediamine, dodecamethylenediamine, and trimethylhexamethylenediamine.

[0127] Examples of aliphatic diacids include adipic, azelaic, suberic, sebacic, and dodecanedicarboxylic acids.

[0128] Among the aliphatic homopolyamides, mention may be made, by way of example and without limitation, of the following polyamides: polycaprolactam (PA6); polyundecanamide (PA 11); polylauryllactam (PA12); polybutylene adipamide (PA4.6); polyhexamethylene adipamide (PA6.6); polyhexamethylene azelamide (PA6.9); polyhexamethylene sebaçamide (PA-6.10); polyhexamethylene dodecanamide (PA6.12); polydecamethylene dodecanamide (PA 10.12); polydecamethylene sebaçamide (PA 10.10) and polydodecamethylene dodecanamide (PA 12.12). PA 6 is particularly preferred.

[0129] Among the cycloaliphatic homopolyamides, we can notably cite those resulting from the condensation of a cycloaliphatic diamine and an aliphatic diacid. As an example of a cycloaliphatic diamine, we can cite 4,4'-methylene-bis(cyclohexylamine), also called para-bis(aminocyclohexyl)methane or PACM, 2,2'-dimethyl-4,4'methylene-bis(cyclohexylamine), also called bis-(3-methyl-4-aminocyclohexyl)-methane or BMACM.

[0130] Among the cycloaliphatic homopolyamides, we can notably mention the polyamides PACM.12, BMACM.10 and BMACM.12.

[0131] Semi-aromatic homopolyamides can result from the condensation of: an aliphatic diamine and an aromatic diacid, such as terephthalic acid (T) and isophthalic acid (I). The polyamides obtained are then commonly called "polyphthalamides" or PPA; an aromatic diamine, such as xylylenediamine, and more particularly metaxylylenediamine (MXD) and an aliphatic diacid.

[0132] In this family of polyamide, we can notably cite polyamides 6.T, 6.I, MXD.6 and MXD.10.

[0133] Alternatively, the polyamide grafts are copolyamides. These result from the polycondensation of at least two of the monomers listed above to obtain homopolyamides.

[0134] The term "monomer" in the present description of copolyamides must be taken in the sense of "repeating unit". Indeed, the case where a repeating unit of the PA is made up of the association of a diacid with a diamine is particular. It is considered that it is the association of a diamine and a diacid, that is to say the diamine-diacid couple (in equimolar quantity), which corresponds to the monomer. This is explained by the fact that individually, the diacid or the diamine is only a structural unit, which is not sufficient on its own to polymerize to give a polyamide.

[0135] Thus, the copolyamides cover in particular the condensation products of at least two lactams, of at least two aliphatic α,δ-aminocarboxylic acids, of at least one lactam and of at least one aliphatic α,δ-aminocarboxylic acid, of at least two diamines and of at least two diacids, of at least one lactam with at least one diamine and at least one diacid, of at least one aliphatic α,δ-aminocarboxylic acid with at least one diamine and at least one diacid,

[0136] The diamine(s) and the diacid(s) may be, independently of one another, aliphatic, cycloaliphatic or aromatic.

[0137] Depending on the types and ratio of monomers, copolyamides can be semi-crystalline or amorphous. Examples of amorphous copolyamides include copolyamides containing semi-aromatic monomers.

[0138] Semi-crystalline copolyamides, particularly PA 6 / 11, PA6 / 12 and PA6 / 11 / 12 copolyamides, can also be used.

[0139] The number-average molecular weight Mn of copolyamides, as measured according to ISO 16014-5:2019, can vary widely, but is advantageously less than 10000 g / mol. Advantageously, the polyamide grafts are monofunctional.

[0140] To make the polyamide graft have a monoamine termination, a chain limiter of the formula can be used:

[0141] RIR2N H in which:

[0142] • R1 is hydrogen or a linear or branched alkyl group containing up to 20 carbon atoms,

[0143] • R2 is a group having up to 20 linear or branched alkyl or alkenyl carbon atoms, a saturated or unsaturated cycloaliphatic radical, an aromatic radical or a combination of the above. The chain limiter can be, for example, laurylamine or oleylamine. For the polyamide graft to have a monocarboxylic acid termination, a chain limiter of formula R'1-COOH, R'1-CO-O-CO- R'2 or a dicarboxylic acid can be used.

[0144] R'1 and R'2 are linear or branched alkyl groups containing up to 20 carbon atoms.

[0145] Advantageously, the polyamide graft has an amine-functional end. Preferred monofunctional polymerization chain limiters are laurylamine and oleylamine. Advantageously, the polyamide grafts have a molar mass of between 1000 and 5000 g / mol and preferably between 2000 and 3000 g / mol.

[0146] The polycondensation defined above is carried out according to known methods, for example at a temperature between 200 and 300°C, under vacuum or in an inert atmosphere, with stirring of the reaction mixture. The average chain length of the graft is determined by the initial molar ratio between the polycondensable monomer or lactam and the chain limiter. For the calculation of the average chain length, one molecule of chain limiter is usually counted for one graft chain.

[0147] A polyamide graft with the desired glass transition and possible melting temperature can be prepared by selecting the appropriate monomer types and ratios. The viscosity of the polyamide graft can be adjusted by modulating the molar mass of the polyamide graft.

[0148] The condensation reaction of the polyamide graft on the polyolefin backbone containing the remainder of (X) is carried out by reaction of an amine or acid function of the polyamide graft on the remainder of (X). Advantageously, monoamine polyamide grafts are used and amide or imide bonds are created by reacting the amine function on the function of the remainder of (X).

[0149] This condensation is preferably carried out in the molten state.

[0150] To manufacture the composition, conventional mixing and / or extrusion techniques can be used. The components of the composition are thus mixed to form a compound that can eventually be granulated at the end of the die. Advantageously, coupling agents are added during compounding.

[0151] To obtain a nanostructured composition, the polyamide graft and the backbone can thus be mixed in an extruder, at a temperature generally between 200 and 300°C. The average residence time of the molten material in the extruder can be between 5 seconds and 5 minutes, and preferably between 20 seconds and 1 minute. The yield of this condensation reaction is evaluated by selective extraction of the free polyamide grafts, i.e. those which have not reacted to form the polyamide graft polymer. The preparation of polyamide grafts with an amine end as well as their addition to a polyolefin backbone containing the remainder of (X) is described in patents US3976720, US3963799, US5342886 and FR2291225. The polyamide graft polymer of the present invention advantageously has a nanostructured organization.To obtain this type of organization, we will preferentially use, for example, grafts having a molar mass in number Mn between 1000 and 5000 g / mol and more preferentially between 2000 and 3000 g / mol.

[0152] The particularly preferred polyamide graft polymer contains the residue of a carboxylic acid anhydride monomer, in particular a maleic anhydride monomer and polyamide 6 (PA6) grafts.

[0153] The grafted polymer comprises 5 to 50% by mass and preferably 15 to 30% by mass of polyamide grafts.

[0154] According to one embodiment, the polyamide grafted polymer has a melting temperature greater than 120°C.

[0155] Advantageously, the melting temperature of the support film is also higher than that of the adhesive layer, which makes it possible to provide thermomechanical stability to the structure. Preferably, the difference between the melting temperature of the support film and the melting temperature of the adhesive layer is between 30 and 60°C.

[0156] According to one embodiment, the support film has a Melt Flow Index (MFI) of between 0.2 and 10 g / 10 min, preferably between 0.4 and 3 g / 10 min, and more preferably between 0.6 and 2 g / 10 min (230°C, 2.16 kg, ASTM D 1238).

[0157] According to another embodiment, the thickness of the support film is between 15 and 60 μm and is in particular of the order of 20 μm. As mentioned above, the support film can be directly in contact with a second adhesive layer so as to form a three-layer structure: adhesive layer / support film / adhesive layer, the second adhesive layer being as defined previously, identical or different from the first. B. Method for preparing the multilayer structure

[0158] The multilayer structure according to the invention can be obtained from the mixtures intended for the adhesive layer and the support film by conventional techniques for producing films, sheets or plates.

[0159] By way of example, the techniques of blown film extrusion (also called "Blown film"), rolling extrusion, coating extrusion, flat film extrusion (also called "cast film") or even sheet extrusion may be cited. All these techniques are known to those skilled in the art and they will be able to adapt the conditions for implementing the different techniques (extruder temperature, connection, dies and "feedblock", screw rotation speed, cooling temperatures of the cooling cylinders, etc.) to form the structure according to the invention having the desired shape and thicknesses. It would not be outside the scope of the invention if the final structure were obtained by pressing techniques, rolling with solvent-based or aqueous adhesives, or if the final structure underwent an additional annealing step.

[0160] The multilayer structure is preferably prepared by coextrusion, particularly by flat film coextrusion.

[0161] When coextruding the two layers, the carrier film layer is usually heated to a higher temperature than the adhesive layer, so that their viscosity, at their respective temperatures, is as close as possible.

[0162] C. Use for the manufacture of a photovoltaic module

[0163] According to a second aspect, the invention relates to the use of a multilayer structure as defined previously for the manufacture of a photovoltaic module.

[0164] The multilayer structure according to the invention is interesting in this application because it greatly facilitates the assembly of the photovoltaic cell with the encapsulant and the upper protective layers (called front-sheet) and on the back of the module (called back-sheet). In particular, this structure is suitable for the manufacture of modules as described in application WO 2004 / 021455 which requires laminating the encapsulant directly to the surface of the interconnectors. Indeed, the good adhesion to the metal of the adhesive layer of the multilayer structure of the invention makes it possible to laminate the interconnectors beforehand onto the multilayer structure, which makes the assembly of the photovoltaic module much simpler.

[0165] It may be advantageous to use the multilayer structure according to the invention with coated interconnectors. In particular, the interconnectors may be coated with a material having a lower melting temperature than that of the adhesive layer, which facilitates soldering to the photovoltaic cell.

[0166] In this use, it is particularly advantageous that the support film forms the protective layer on the back of the photovoltaic module called the "backsheet" of the photovoltaic module.

[0167] D. Photovoltaic module

[0168] According to yet another aspect, the invention relates to a photovoltaic module comprising at least one multilayer structure as described above.

[0169] The multilayer structure can serve in particular as an encapsulant for at least one photovoltaic cell (10). The support film of the multilayer structure can also, according to a preferred embodiment, serve as a protective layer on the back of the module ("back-sheet") (26).

[0170] E. Manufacturing process of a photovoltaic module

[0171] According to yet another aspect, the invention relates to a method for preparing a photovoltaic module comprising a step of encapsulating at least one photovoltaic cell (10) with a multilayer structure as defined previously.

[0172] The multilayer structure, more particularly the adhesive layer thereof, is in particular in direct contact with said photovoltaic cell (10), in particular with at least one electrical interconnector (18) connecting two photovoltaic cells (12).

[0173] According to one embodiment, the step of encapsulating at least one photovoltaic cell (10) comprises the steps of: i) bringing the adhesive layer (22) of the multilayer structure into contact with at least one electrical interconnector (18) at a temperature lower than the melting temperature of the adhesive layer (22), in particular 5 to 20°C lower than the melting temperature of the adhesive layer (22), conventionally at a temperature between 70 and 80°C, whereby at least one electrical interconnector (18) is obtained fixed to the surface of the adhesive layer of the multilayer structure; ii) Laminating the multilayer structure fixing at least one electrical interconnector obtained in the previous step onto the other components of the photovoltaic cell (10), in particular at a temperature between the melting temperature of the adhesive layer and the flow temperature of the backsheet, in particular between 140 and 160°C.

[0174] According to a particular embodiment, the electrical interconnectors (18) may in particular be arranged on the surface of the adhesive layer (22), of the multilayer structure in the form of wires or parallel strips. They may be fixed to the surface of the adhesive layer (22), by contacting with the adhesive layer (22), which may have been heated to a temperature of between 50 and 100°C so as to make it sticky. The multilayer structure, incorporating the interconnectors (18), obtained in step i) may then be arranged on the other components of the photovoltaic module, in particular the photovoltaic cells (10).

[0175] To facilitate module assembly, the interconnectors can be coated with a polymer having a lower temperature than the adhesive layer.

[0176] Preferably, the peel strength of the interface between the adhesive layer (22) and the metal filaments used as electrical interconnectors (18) in the module is at least 0.1 N / cm, preferably at least 0.2 N / cm at a 90° angle, at room temperature.

[0177] EXAMPLES

[0178] Materials used Polyolefins A

[0179] A Affinity PL1880G: Ethylene-octene copolymer, marketed by Dow Chemicals B EVA 1010 VN3: Ethylene and vinyl acetate copolymer, marketed by Total

[0180] C LDPE 1022 FN24: Linear low density polyethylene, marketed by Total

[0181] Functionalized polyolefin

[0182] Lotader® 3210: terpolymer of ethylene, butyl acrylate and maleic anhydride, marketed by SK Functional Polyolefins Additives

[0183] Adhesive masterbatch MB4 marketed by Arkema France: glass adhesion promoter containing a silane UVB masterbatch: masterbatch containing an Apolhya Solar® LP91H3-UVB UV stabilizer containing 80% by weight of polyolefin forming a trunk with maleic anhydride functions linked to 20% by weight of polyamide 6 grafts. The product has an MFI (“Melt Flow Index”) of 0.5 g / 10 min at 230°C under 2.16 kg and a melting point of 216°C

[0184] Apolhya Solar® LC3-UV contains 80% by weight of polyolefin forming a backbone with maleic anhydride functions linked to 20% by weight of copolyamide 6.12 grafts. The product has an MFI (Melt Flow Index) of 10 g / 10 min at 230°C under 2.16 kg and a melting point of 130°C. [Table 1]

[0185] Film preparation

[0186] Films 70 μm thick were produced by flatbed film extrusion (CAST) on a Dr. COLLIN extrusion line. This extrusion line consists of three extruders equipped with a standard polyolefin screw profile, a variable feed block, and a 250 mm coat hanger die. The feed block allows the production of a two-layer film (Layer 1 / Layer 2) with a variable thickness distribution. EXAMPLES 1 to 3

[0187] The adhesive layer formulations were prepared by dry-blending a functionalized polyolefin and a polyolefin A as shown in Table 1 below. Then, films comprising an adhesive layer and a carrier film were prepared by co-extrusion as shown in Table 1 under the following conditions:

[0188] Adhesive layer extrusion temperature: 150°C, Support film extrusion temperature: 240°C, Coextrusion head and die temperature: 220°C, Line speed: 6 m / min.

[0189] EXAMPLE 4 (COMPARATIVE)

[0190] A film was prepared by co-extrusion as indicated in the preceding examples except for replacing the functionalized polyolefin and polyolefin A formulation with Apolyha Solar LC3-UV.

[0191] EXAMPLE 5 (COMPARATIVE)

[0192] A monolayer film of Apolhya Solar LP91H3-UVB was prepared by extrusion under the following conditions:

[0193] Extrusion temperature, coextrusion head and die: 240°C,

[0194] Line speed: 6 m / min.

[0195] Evaluation of the films The films were characterized by measuring the melting temperature of the adhesive layer, by DSC according to the ISO11357-1 / -3 standard.

[0196] Furthermore, the adhesion between the films and the metal filaments used as connections of the photovoltaic modules was evaluated according to the following protocol:

[0197] 10 tin filaments with a diameter of 25 pm are placed side by side in parallel in contact with the adhesive layer of the films; Welding is carried out by pressing at 130°C under 5 bars for 2 s; and

[0198] The adhesion strength between the filaments and the film is assessed by means of a free-angle peel test, using a dynamometer in which the filaments are held by one jaw and the film by the other. The equilibrium force is measured during delamination propagation.

[0199] The results of these evaluations are presented in Table 2 below.

[0200] [Table 2]

[0201] These results show that the multilayer structures according to the invention are characterized by a peel strength greater than those obtained with a structure whose adhesive layer does not comprise a combination of functional polyolefin / and a polyolefin A as defined in the present invention, but rather a polyolefin grafted with polyamide grafts with a melting point of 130°C (Example 4) or single-layer structures (Example 5).

[0202] Furthermore, these results show that adhesive layer matrices with a melting point between 80 and 120°C can significantly increase adhesion to metal filaments.

Claims

Claims 1. Multilayer structure comprising an adhesive layer and a layer forming a support film in direct contact therewith, wherein (a) said adhesive layer comprises: a polyolefin A chosen from a homopolymer of ethylene and a copolymer of ethylene and an α-olefin, a copolymer of ethylene and a vinyl ester of carboxylic acid, in particular a vinyl acetate (EVA) or a (co)polymer comprising methyl, ethyl, propyl, n-butyl, sec-butyl, isobutyl or tert-butyl (meth)acrylate units; and a functionalized polyolefin, distinct from polyolefin A, comprising a polyolefin backbone containing a residue of at least one unsaturated monomer (Y), the remainder of the unsaturated monomer (Y) being attached to the backbone by grafting or copolymerization;the melting temperature of the adhesive layer being between 80°C and 120°C, b) said support film comprises a polyamide graft polymer comprising: a polyolefin backbone, representing from 50% to 95% by mass of the polyamide graft polymer, containing a remainder of at least one unsaturated monomer (X) and at least one polyamide graft, representing from 5% to 50% by mass of said polyamide graft polymer, in which: o the polyamide graft is attached to the polyolefin backbone by the remainder of the unsaturated monomer (X) comprising a function capable of reacting by a condensation reaction with a polyamide having at least one amine end and / or at least one carboxylic acid end, o the remainder of the unsaturated monomer (X) is attached to the backbone by grafting or copolymerization,; o The polyolefin backbone and the polyamide graft being chosen so that said polyamide graft polymer has a flow temperature above 160°C, as measured by DSC according to ISO 11357-1:2016, ISO 11357-2:2020, ISO 11357-3:2018, said flow temperature being defined as the highest of the melting temperatures and the glass transition temperatures of the polyamide graft and the polyolefin backbone. Multilayer structure according to claim 1, wherein the melting temperature of said adhesive layer is between 90°C and 110°C. Multilayer structure according to any one of the preceding claims, wherein said adhesive layer has a Melt Flow Index (MFI), as measured according to ASTP D 1238 at 190°C under 2.16 kg, of between 0.2 and 10 g / 10 min, preferably between 0.4 and 3 g / 10 min, and in particular between 0.6 and 2 g / 10 min.Multilayer structure according to one of claims 1 to 3, in which said adhesive layer comprises: from 65% to 95% by weight of polyolefin A; from 5 to 35% by weight of functional polyolefin; and from 0 to 5% by weight of one or more additives. Multilayer structure according to one of claims 1 to 4, in which the thickness of said adhesive layer is between 20 and 60 μm. Multilayer structure according to one of claims 1 to 5, in which the thickness of said support film is between 5 and 40 μm. Multilayer structure according to one of claims 1 to 6, wherein the α-olefin comonomer of polyolefin A of the adhesive layer is selected from ethylene-propylene, ethylene-butene and ethylene-octene. Multilayer structure according to one of claims 1 to 7, wherein the functional polyolefin of said adhesive layer is a polyolefin containing a residue of at least one unsaturated monomer (Y) which is a maleic anhydride. Multilayer structure according to one of claims 1 to 8, wherein said support film has a Melt Flow Index (MFI), as measured according to ASTP D 1238 at 230°C under 2.16 kg, of between 0.2 and 10 g / 10 min, preferably between 0.4 and 3 g / 10 min, in particular between 0.6 and 2 g / 10 min. Multilayer structure according to one of claims 1 to 9, characterized in that said support film carries said adhesive layer on one of its faces.Multilayer structure according to one of claims 1 to 9, characterized in that said support film carries said adhesive layer on both sides. Method for preparing a multilayer structure according to one of claims 1 to 11, in which said support film is assembled to said adhesive layer by coextrusion. Use of a multilayer structure according to one of claims 1 to 11 for the manufacture of photovoltaic modules. Method for preparing a photovoltaic module, in which a photovoltaic cell is encapsulated with a multilayer structure according to one of claims 1 to 11. The method of claim 14, wherein the encapsulation comprises the steps of: (i) attaching an electrically conductive filament to the surface of the adhesive layer of a multilayer structure according to one of claims 1 to 11 at a temperature below the melting temperature of the adhesive layer to form an assembly; (ii) bringing said assembly into contact with a photovoltaic cell at a temperature between the melting temperature of the adhesive layer and the flow temperature of the support film. Photovoltaic module comprising a multilayer structure as defined in claims 1 to 11.

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