Multilayer film with polyamide and polyester layers for the production of photovoltaic modules

Abstract

A multilayer film containing layers of polyamide and polyester, suitable as a back cover for a photovoltaic module is provided. The film comprises, in the order listed: a) a layer which comprises at least 35% by weight of polyamide; c) a layer which comprises at least 35% by weight, of a thermoplastic polyester; and e) a layer which comprises at least 35% by weight of polyamide; wherein the layers a) and e) further comprise 0.1 to 60% by weight, of a polyamine-polyamide graft copolymer, or the layer c) further comprises 0.1 to 30% by weight of polyamine-polyamide graft copolymer. The polyamine-polyamide graft copolymer comprises as copolymerized monomers: a polyamine having at least 4 nitrogen atoms and at least one polyamide-forming unit selected from the group consisting of a lactam, an -aminocarboxylic acid and an equimolar combinations of a diamine and a dicarboxylic acid. In another embodiment, adhesion promoting layers are placed between the layers.

Claims

1. A multilayer film, comprising, in the order listed: a) a first layer of from 15 to 100 m in thickness having a composition which comprises a light reflecting filler and at least 35% by weight of polyamide based on the weight of the composition of the first layer; c) a second layer of from 100 to 500 m in thickness having a composition which comprises a polyamide, at least one of a reinforcing filler and a light reflecting filler and at least 35% by weight of a thermoplastic polyester based on the weight of the composition of the second layer; e) a third layer of from 15 to 100 m in thickness having a composition which comprises at least one of a reinforcing filler and a light reflecting filler and at least 35% by weight of polyamide based on the weight of the composition of the third layer; wherein the thickness of the first layer is independent of the thickness of the third layer, the compositions of the first and third layers each further comprise 0.1 to 60% by weight of a polyamine-polyamide graft copolymer, or the composition of the second layer further comprises 0.1 to 30% by weight of polyamine-polyamide graft copolymer; with the proviso that the polyamine-polyamide graft copolymer comprises as copolymerized monomers: 0.5 to 25% by weight, based on the weight of the graft copolymer, of a polyamine having at least 4 nitrogen atoms and at least one polyamide-forming unit selected from the group consisting of a lactam, an -aminocarboxylic acid and an equimolar combination of a diamine and a dicarboxylic acid.

2. The multilayer film according to claim 1 wherein the thermoplastic polyester of the second layer is a linear polyester comprising polycondensed diols and dicarboxylic acids or polyester-forming derivatives thereof wherein the diol is of formula
HOROH wherein R is a divalent branched or unbranched aliphatic and/or cycloaliphatic radical having 2 to 40 carbon atoms, and the dicarboxylic acid is of formula
HOOCRCOOH wherein R is a divalent aromatic radical having 6 to 20 carbon atoms.

3. The multilayer film according to claim 1, wherein the polyamide present in at least 35% of each of the first and third layers comprises independently one selected from the group consisting of a partly crystalline polyamide having an enthalpy of fusion of more than 25 J/g, a semicrystalline polyamide having an enthalpy of fusion of from 4 to 25 J/g and an amorphous polyamide having an enthalpy of fusion of less than 4 J/g.

4. The multilayer film according to claim 1 wherein the polyamide present in at least 35% of the first layer, the polyamide present in at least 35% of the third layer or both the polyamides present in at least 35% of the first layer and the third layer comprises at least one of a polyetheresteramide and a polyetheramide.

5. A photovoltaic module, comprising; a solar cell embedded in a sealing layer; and the multilayer film according to claim 1 as a back cover; wherein the first layer of the multilayer film is bonded to the sealing layer.

6. The photovoltaic module according to claim 5, wherein at least one of the first layer, the third layer and the second layer further comprises an impact-modifying rubber optionally modified with a polyamide compatible functional group.

7. The multilayer film of claim 1, further comprising: b) optionally, an adhesion promoter layer between the first and second layer; and d) optionally, an adhesion promoter layer between the second and third layer; wherein at least one adhesion promoter layer is present, and comprises: 0.1 to 100% by weight of a polyamine-polyamide graft copolymer, 0 to 99.9% by weight of a polyamide and 0 to 99.9% by weight of a thermoplastic polyester, with the proviso that the polyamine-polyamide graft copolymer comprises as copolymerized monomers: 0.5 to 25% by weight, based on the weight of the graft copolymer, of a polyamine having at least 4 nitrogen atoms and at least one polyamide-forming unit selected from the group consisting of a lactam, an -aminocarboxylic acid and an equimolar combinations of a diamine and a dicarboxylic acid.

8. The multilayer film according to claim 7, wherein the polyamine of the graft copolymer is one selected from the group consisting of a polyvinylamine, a polyamine prepared from an alternating polyketone, a dendrimer, a linear polyethyleneimine, and a branched polyethyleneimine.

9. The multilayer film according to claim 8 wherein a number average molecular weight of the polyamine is not greater than 20,000 g/mol.

10. A photovoltaic module, comprising; a solar cell embedded in a sealing layer; and the multilayer film according to claim 7 as a back cover; wherein the first layer of the laminate film is bonded to the sealing layer.

11. The multilayer film of claim 1, wherein at least one of the second layer c) and the third layer e) comprise a reinforcing filler.

12. The multilayer film of claim 1, wherein the second layer c) and the third layer e) comprise a reinforcing filler.

13. The multilayer film of claim 1, wherein at least one of the second layer c) and the third layer e) comprise a reinforcing filler and the reinforcing filler is glass fibers.

14. The multilayer film of claim 1, wherein the second layer c) and the third layer e) comprise a reinforcing filler and the reinforcing filler is glass fibers.

Description

DETAILED DESCRIPTION OF THE INVENTION

(1) The first embodiment of the invention provides a multilayer film, comprising, in the order listed:

(2) a) a layer of a moulding composition which comprises at least 35% by weight, based on the overall layer moulding composition, of polyamide;

(3) c) a layer of a moulding composition which comprises at least 35% by weight, based on the overall layer moulding composition, of a thermoplastic polyester;

(4) e) a layer of a moulding composition which comprises at least 35% by weight, based on the overall moulding composition, of polyamide;

(5) wherein

(6) the layers a) and e) further comprise 0.1 to 60% by weight, based on the respective moulding composition, of a polyamine-polyamide graft copolymer, or

(7) the layer c) further comprises 0.1 to 30% by weight, based on the moulding composition, of polyamine-polyamide graft copolymer;

(8) with the proviso that the polyamine-polyamide graft copolymer comprises as copolymerized monomers:

(9) 0.5 to 25% by weight, based on the weight of the graft copolymer, of a polyamine having at least 4 nitrogen atoms and

(10) at least one polyamide-forming unit selected from the group consisting of a lactam, an -aminocarboxylic acid and an equimolar combinations of a diamine and a dicarboxylic acid.

(11) In the layer a) which is a solar cell-facing layer the polyamide content is preferably at least 40% by weight, more preferably at least 45% by weight, especially preferably at least 50% by weight and most preferably at least 55% by weight, based in each case on the overall moulding composition,

(12) In the layer c) the content of the thermoplastic polyester is preferably at least 40% by weight, more preferably at least 45% by weight, especially preferably at least 50% by weight and most preferably at least 55% by weight, based in each case on the overall moulding composition, and

(13) In the layer e) the polyamide content is preferably at least 40% by weight, more preferably at least 45% by weight, especially preferably at least 50% by weight and most preferably at least 55% by weight, based in each case on the overall moulding composition.

(14) The content of the polyamine-polyamide graft copolymer in the layer a) and/or the layer e) is preferably in each case 1 to 50% by weight and more preferably in each case 3 to 40% by weight, based on the respective moulding composition, of polyamine-polyamide graft copolymer.

(15) The content of the polyamine-polyamide graft copolymer in the layer c) is preferably 1 to 20% by weight, based on the moulding composition.

(16) In a preferred embodiment, the invention provides a photovoltaic module, comprising;

(17) a solar cell embedded in a sealing layer; and

(18) the multilayer film according to the first embodiment as a back cover;

(19) wherein the layer a) of the laminate film is bonded to the sealing layer.

(20) In a second embodiment, the present invention provides a multilayer film, comprising, in the order listed:

(21) a) a layer of a moulding composition which comprises at least 35% by weight, based on the overall layer moulding composition, of polyamide;

(22) b) optionally, an adhesion promoter layer;

(23) c) a layer of a moulding composition which comprises at least 35% by weight, based on the overall layer moulding composition, of a thermoplastic polyester;

(24) d) optionally, an adhesion promoter layer; and

(25) e) a layer of a moulding composition which comprises at least 35% by weight, based on the overall moulding composition, of polyamide;

(26) wherein

(27) at least one of layer b) or layer d) is present,

(28) the at least one of layer b or d) comprises 60 to 100% by weight of: 0.1 to 100% by weight of a polyamine-polyamide graft copolymer, 0 to 99.9% by weight of a polyamide and 0 to 99.9% by weight of a thermoplastic polyester,

(29) with the proviso that the polyamine-polyamide graft copolymer comprises as copolymerized monomers: 0.5 to 25% by weight, based on the weight of the graft copolymer, of a polyamine having at least 4 nitrogen atoms and

(30) at least one polyamide-forming unit selected from the group consisting of a lactam, an -aminocarboxylic acid and an equimolar combinations of a diamine and a dicarboxylic acid.

(31) In the layer a) which is a solar cell-facing layer the polyamide content is preferably at least 40% by weight, more preferably at least 45% by weight, especially preferably at least 50% by weight and most preferably at least 55% by weight, based in each case on the overall moulding composition,

(32) In the layer c) the content of the thermoplastic polyester is preferably at least 40% by weight, more preferably at least 45% by weight, especially preferably at least 50% by weight and most preferably at least 55% by weight, based in each case on the overall moulding composition, and

(33) In the layer e) the polyamide content is preferably at least 40% by weight, more preferably at least 45% by weight, especially preferably at least 50% by weight and most preferably at least 55% by weight, based in each case on the overall moulding composition.

(34) In the adhesion promoying layers the content of the polyamine-polyamide graft copolymer is preferably 1 to 75% by weight, more preferably 3 to 50% by weight and especially preferably 4 to 40% by weight.

(35) In the adhesion promoying layers the content of the polyamide is preferably 12.5 to 99% by weight, more preferably 25 to 97% by weight and especially preferably 30 to 96% by weight.

(36) In the adhesion promoying layers the content of the thermoplastic polyester is preferably 12.5 to 99% by weight, more preferably 25 to 97% by weight and especially preferably 30 to 96% by weight.

(37) In the adhesion promoying layers the content of the additives selected from impact-modifying rubber and standard assistants and admixtures is preferably 0.1 to 30% by weight.

(38) In the adhesion promoying layers the content of thepolyamine in the polyamine-polyamide graft copolymer is preferably 1 to 20% by weight and more preferably 1.5 to 16% by weight, based on the graft copolymer.

(39) In another preferred embodiment the present invention provides A photovoltaic module, comprising;

(40) a solar cell embedded in a sealing layer; and

(41) the multilayer film according to the second embodiment as a back cover;

(42) wherein the layer a) of the laminate film is bonded to the sealing layer.

(43) Thus, various arrangements of the invention may be as follows:

(44) In one arrangement, the multilayer film comprises, in direct succession, the layers a), c) and e). Both the moulding composition of the layer a) and the moulding composition of the layer e) comprise the polyamine-polyamide graft copolymer as described.

(45) In a second arrangement, the multilayer film comprises, in direct succession, the layers a), c) and e). The moulding composition of the layer c) comprises the polyamine-polyamide graft copolymer as described above.

(46) In a third arrangement, the multilayer film comprises, in direct succession, the layers a), b), c), d) and e). The layers b) and d) are adhesion promoter layers having a composition as described above.

(47) In a fourth arrangement, the multilayer film comprises, in direct succession, the layers a), c), d) and e). The moulding composition of the layer according to a) comprises the amount of polyamine-polyamide graft copolymer as described above. The layer according to d) is an adhesion promoter layer having a composition as described above.

(48) In a fifth arrangement, the multilayer film comprises, in direct succession, the layers a), b), c) and e). The moulding composition of the layer e) comprises the amount of polyamine-polyamide graft copolymer described above. The layer b) is an adhesion promoter layer having a composition as described above.

(49) Unless stated otherwise, the further details which follow may apply equally to all these arrangements.

(50) The polyamide may be a partly crystalline polyamide, for example PA6, PA66, PA610, PA612, PA10, PA810, PA106, PA1010, PA11, PA1011, PA1012, PA1210, PA1212, PA814, PA1014, PA618, PA512, PA613, PA813, PA914, PA1015, PA11, PA12, or a semiaromatic polyamide, called a polyphthalamide (PPA). (The naming of the polyamides corresponds to the international standard, the first number(s) giving the number of carbon atoms of the starting diamine and the last number(s) the number of carbon atoms of the dicarboxylic acid. If only one number is mentioned, this means that the starting material was an ,-aminocarboxylic acid or the lactam derived therefrom; for the rest, reference is made to H. Domininghaus, Die Kunststoffe and ihre Eigenschaften [The polymers and their properties], pages 272 ff., VDI-Verlag, 1976.) Suitable PPAs are, for example, PA66/6T, PA6/6T, PA6T/MPMDT (MPMD stands for 2-methylpentamethylenediamine), PA9T, PA10T, PA11T, PA12T, PA14T and copolycondensates of these latter types with an aliphatic diamine and an aliphatic dicarboxylic acid or with an w-aminocarboxylic acid or a lactam. Partly crystalline polyamides have an enthalpy of fusion of more than 25 J/g, measured by the DSC method to ISO 11357 in the 2nd heating step and integration of the melt peak.

(51) The polyamide may also be a semicrystalline polyamide. Semicrystalline polyamides have an enthalpy of fusion of 4 to 25 J/g, measured by the DSC method to ISO 11357 in the 2nd heating step and integration of the melt peak. Examples of suitable semicrystalline polyamides are The polyamide of 1,10-decanedioic acid or 1,12-dodecanedioic acid and 4,4-diaminodicyclohexylmethane (PA PACM10 and PA PACM12), proceeding from a 4,4-diaminodicyclohexylmethane with a trans,trans isomer content of 35 to 65%; copolymers based on the abovementioned partly crystalline polyamides; and blends of the abovementioned partly crystalline polyamides and a compatible amorphous polyamide.

(52) The polyamide may also be an amorphous polyamide. Amorphous polyamides have an enthalpy of fusion of less than 4 J/g, measured by the DSC method to ISO 11357 in the 2nd heating step and integration of the melt peak. Examples of amorphous polyamides are: the polyamide of terephthalic acid and/or isophthalic acid and the isomer mixture of 2,2,4- and 2,4,4-trimethylhexamethylenediamine, the polyamide of isophthalic acid and 1,6-hexamethylenediamine, the copolyamide of a mixture of terephthalic acid/isophthalic acid and 1,6-hexamethylenediamine, optionally in a mixture with 4,4-diaminodicyclohexylmethane, the copolyamide of terephthalic acid and/or isophthalic acid, 3,3-dimethyl-4,4-diaminodicyclohexylmethane and laurolactam or caprolactam, the (co)polyamide of 1,12-dodecanedioic acid or sebacic acid, 3,3-dimethyl-4,4-diaminodicyclohexylmethane, and optionally lauro-lactam or caprolactam, the copolyamide of isophthalic acid, 4,4-diaminodicyclohexylmethane and laurolactam or caprolactam, the polyamide of 1,12-dodecanedioic acid and 4,4-diaminodicyclohexylmethane (in the case of a low trans,trans isomer content), the (co)polyamide of terephthalic acid and/or isophthalic acid and an alkyl-substituted bis(4-aminocyclohexyl)methane homologue, optionally in a mixture with hexamethylenediamine, the copolyamide of bis(4-amino-3-methyl-5-ethylcyclohexyl)methane, optionally together with a further diamine, and isophthalic acid, optionally together with a further dicarboxylic acid, the copolyamide of a mixture of m-xylylenediamine and a further diamine, e.g. hexamethylenediamine, and isophthalic acid, optionally together with a further dicarboxylic acid, for example terephthalic acid and/or 2,6-naphthalenedicarboxylic acid, the copolyamide of a mixture of bis(4-aminocyclohexyl)methane and bis(4-amino-3-methylcyclohexyl)methane, and aliphatic dicarboxylic acids having 8 to 14 carbon atoms, and polyamides or copolyamides of a mixture comprising 1,14-tetradecanedioic acid and an aromatic, arylaliphatic or cycloaliphatic diamine.

(53) These examples may be varied to a very substantial degree by addition of further components (for example caprolactam, laurolactam or diamine/dicarboxylic acid combinations) or by partial or full replacement of starting components by other components.

(54) The polyamide may also be a polyetheresteramide or a polyetheramide. Polyetheresteramides are described, for example, in DE-A-25 23 991 and DE-A-27 12 987; they contain a polyether diol as a comonomer. Polyetheramides are described, for example, in DE-A-30 06 961; they contain a polyether diamine as a comonomer.

(55) In the polyether diol or the polyether diamine, the polyether unit may be based, for example, on 1,2-ethanediol, 1,2-propanediol, 1,3-propanediol, 1,4-butanediol or 1,3-butanediol. The polyether unit may also be of mixed structure, for instance with random or blockwise distribution of the units originating from the diols. The weight-average molar mass of the polyether diols or polyether diamines may be 200 to 5000 g/mol and preferably 400 to 3000 g/mol; the proportion thereof in the polyetheresteramide or polyetheramide may preferably be 4 to 60% by weight and more preferably 10 to 50% by weight. Suitable polyether diamines are obtainable by conversion of the corresponding polyether diols by reductive amination or coupling to acrylonitrile with subsequent hydrogenation; they are commercially available, for example, in the form of the JEFFAMINE D or ED products or of the ELASTAMINE products from Huntsman Corp., or in the form of the Polyetheramine D series from BASF SE. It may also be possible to additionally use smaller amounts of a polyether triamine, for example a JEFFAMINE T product, if a branched polyetheramide is to be used. Preference is given to using polyether diamines or polyether triamines which contain an average of at least 2.3 carbon atoms in the chain per ether oxygen atom. According to the invention, polyetheramides are preferred due to better hydrolysis resistance.

(56) Useful thermoplastic polyesters include linear thermoplastic polyesters. These may be prepared by polycondensation of diols with dicarboxylic acid or polyester-forming derivatives thereof such as dimethyl esters. Suitable diols may have the formula HOROH where R is a divalent branched or unbranched aliphatic and/or cycloaliphatic radical having 2 to 40 and preferably 2 to 12 carbon atoms. Suitable dicarboxylic acids may have the formula HOOCR13 COOH where R is a divalent aromatic radical having 6 to 20 and preferably 6 to 12 carbon atoms.

(57) Examples of diols include ethylene glycol, trimethylene glycol, tetramethylene glycol, hexamethylene glycol, neopentyl glycol, cyclohexanedimethanol, and the C36 diol dimer diol. The diols can be used alone or as a diol mixture. Up to 25 mol % of the diol mentioned may be replaced by a polyalkylene glycol of the formula:

(58) ##STR00001##

(59) wherein R is a divalent radical having 2 to 4 carbon atoms and x is a value from 2 to 50.

(60) Examples of useful aromatic dicarboxylic acids include terephthalic acid, isophthalic acid, 1,4-, 1,5-, 2,6- or 2,7-naphthalenedicarboxylic acid, diphenic acid and diphenyl ether 4,4-dicarboxylic acid. Up to 30 mol % of these dicarboxylic acids may be replaced by aliphatic or cycloaliphatic dicarboxylic acids, for example succinic acid, adipic acid, sebacic acid, dodecanedioic acid or cyclohexane-1,4-dicarboxylic acid.

(61) Examples of suitable polyesters include polyethylene terephthalate, polypropylene terephthalate, polybutylene terephthalate, polyethylene 2,6-naphthalate, polypropylene 2,6-naphthalate and polybutylene 2,6-naphthalate.

(62) The preparation of these polyesters is described in DE-A 24 07 155, 24 07 156; Ullmanns Encyclopdie der technischen Chemie, 4th ed., Vol. 19, pages 65 ff., Verlag Chemie, Weinheim, 1980).

(63) The polyamines used in the polyamine-polyamide graft copolymer may, for example, be the following substance classes: polyvinylamines (Rompp Chemie Lexikon, 9th edition, volume 6, page 4921, Georg Thieme Verlag Stuttgart 1992) polyamines which are prepared from alternating polyketones (DE-A 196 54 058) dendrimers, for example ((H2N(CH2)3)2N(CH2)3)2-N(CH2)2-N((CH2)2-N((CH2)3-NH2)2)2 (DE-A-196 54 179) or

(64) tris(2-aminoethyl)amine, N,N-bis(2-aminoethyl)-N,N-bis[2-[bis(2-aminoethyl)amino]ethyl]-1,2-ethanediamine,

(65) 3,15-bis(2-aminoethyl)-6,12-bis[2-[bis(2-aminoethyl)amino]ethyl]-9-[2-[bis[2-bis(2-aminoethyl)amino]ethyl]amino]ethyl]-3,6,9,12,15-pentaazaheptadecane-1,17-diamine (J. M. Warakomski, Chem. Mat. 1992, 4, 1000-1004); linear polyethyleneimines which can be prepared by polymerization of 4,5-dihydro-1,3-oxazoles and subsequent hydrolysis (Houben-Weyl, Methoden der Organischen Chemie [Methods of Organic Chemistry], Volume E20, pages 1482-1487, Georg Thieme Verlag Stuttgart, 1987); branched polyethyleneimines which are obtainable by polymerization of aziridines (Houben-Weyl, Methoden der Organischen Chemie, Volume E20, pages 1482-1487, Georg Thieme Verlag Stuttgart, 1987) and which generally have the following amino group distribution:

(66) 25 to 46% primary amino groups,

(67) 30 to 45% secondary amino groups and

(68) 16 to 40% tertiary amino groups.

(69) In a preferred case, the polyamine may have a number-average molecular weight Mn not exceeding 20 000 g/mol, more preferably not exceeding 10 000 g/mol and especially preferably not exceeding 5 000 g/mol.

(70) Lactams or co-aminocarboxylic acids which may be used as polyamide-forming monomers contain 4 to 19 and especially 6 to 12 carbon atoms. Particular preference may be given to using caprolactam, w-aminocaproic acid, caprylolactam, co-aminocaprylic acid, laurolactam, co-aminododecanoic acid and/or co-aminoundecanoic acid.

(71) Combinations of diamine and dicarboxylic acid may be, for example, hexamethylenediamine/adipic acid, hexamethylenediamine/dodecanedioic acid, octamethylenediamine/sebacic acid, decamethylenediamine/sebacic acid, decamethylenediamine/dodecanedioic acid, dodecamethylenediamine/dodecanedioic acid and dodecamethylenediamine/2,6-naphthalenedicarboxylic acid. In addition, it may also be possible to use all other combinations, such as decamethylenediamine/dodecanedioic acid/terephthalic acid, hexamethylenediamine/adipic acid/terephthalic acid, hexamethylenediamine/adipic acid/caprolactam, decamethylenediamine/dodecanedioic acid/co-aminoundecanoic acid, decamethylenediamine/dodecanedioic acid/laurolactam, decamethylenediamine/terephthalic acid/laurolactam or dodecamethylenediamine/2,6-naphthalenedicarboxylic acid/laurolactam.

(72) In a preferred embodiment, the graft copolymer may additionally be prepared using an oligocarboxylic acid selected from 0.015 to about 3 mol % of dicarboxylic acid and 0.01 to about 1.2 mol % of tricarboxylic acid, based in each case on the sum of the rest of the polyamide-forming monomers. On this basis, each of these monomers is considered individually in the equivalent combination of diamine and dicarboxylic acid. In this way, the polyamide-forming monomers overall have a slight excess of carboxyl groups. When a dicarboxylic acid is used, preferably 0.03 to 2.2 mol %, more preferably 0.05 to 1.5 mol %, even more preferably 0.1 to 1 mol % and especially 0.15 to 0.65 mol % is added; if a tricarboxylic acid is used, preferably 0.02 to 0.9 mol %, more preferably 0.025 to 0.6 mol %, even more preferably 0.03 to 0.4 mol % and especially 0.04 to 0.25 mol % is taken. The additional use of the oligocarboxylic acid distinctly improves hydrolysis resistance and stress-cracking resistance.

(73) The oligocarboxylic acid used may be any desired di- or tricarboxylic acid having 6 to 24 carbon atoms, for example adipic acid, suberic acid, azelaic acid, sebacic acid, dodecanedioic acid, isophthalic acid, 2,6-naphthalenedicarboxylic acid, cyclohexane-1,4-dicarboxylic acid, trimesic acid and/or trimellitic acid.

(74) In addition, if desired, aliphatic, alicyclic, aromatic, aralkylic and/or alkylaryl-substituted monocarboxylic acids having 3 to 50 carbon atoms, for example lauric acid, unsaturated fatty acids, acrylic acid or benzoic acid, can be used as regulators. These regulators can be used to reduce the concentration of amino groups without altering the molecular skeleton. In addition, it is possible in this way to introduce functional groups such as double or triple bonds etc. It is, however, desirable that the graft copolymer has a substantial proportion of amino groups. In a preferred embodiment, the amino group concentration of the graft copolymer may be in the range from 100 to 2500 mmol/kg, more preferably in the range from 150 to 1500 mmol/kg, especially preferably in the range from 250 to 1300 mmol/kg and most preferably in the range from 300 to 1100 mmol/kg. Amino groups are understood here and hereinafter to mean not just amino end groups but also any secondary or tertiary amino functions present in the polyamine.

(75) The inventive graft copolymers may be prepared by various processes.

(76) One option may be to initially charge lactam or co-aminocarboxylic acid and polyamine together and to conduct the polymerization or the polycondensation. The oligocarboxylic acid may be added either at the start or in the course of the reaction.

(77) However, a preferred process involves, in a two-stage process, first conducting the lactam cleavage and prepolymerization in the presence of water (alternatively, the corresponding -aminocarboxylic acids or diamines and dicarboxylic acids are used directly and prepolymerized); in the second step, the polyamine is added, while any oligocarboxylic acid additionally used is metered in before, during or after the prepolymerization. Then the mixture is decompressed at temperatures between 200 and 290 C. and polycondensed in a nitrogen stream or under reduced pressure.

(78) A further preferred process involves the hydrolytic degradation of a polyamide to a prepolymer and simultaneous or subsequent reaction with the polyamine. Preference is given to using polyamides in which the end group difference is approximately zero, or in which any oligocarboxylic acid additionally used has already been incorporated by polycondensation. The oligocarboxylic acid can also be added at the start of or in the course of the degradation reaction. These processes may be used to prepare ultrahighly branched polyamides with acid numbers less than 40 mmol/kg, preferably less than 20 mmol/kg and more preferably less than 10 mmol/kg. Even after a reaction time of one to five hours at temperatures of 200 C. to 290 C., virtually full conversion is achieved.

(79) If desired, in a further process step, a vacuum phase lasting several hours may follow. This lasts at least four hours, preferably at least six hours and more preferably at least eight hours at 200 to 290 C. After an induction period of several hours, an increase in the melt viscosity is then observed, which may be attributable to the fact that a reaction of amino end groups with one another takes place with elimination of ammonia and chain linkage. As a result, the molecular weight is increased further, which is advantageous especially for extrusion moulding compositions.

(80) If the intention is not to conduct the reaction to completion in the melt, the ultrahighly branched polyamide may also be postcondensed in solid phase as conventionally known.

(81) The moulding composition of the layer according to a) may comprise either one of the abovementioned polyamides or a plurality thereof as a mixture. In addition, up to 40% by weight, based on the total polymer content of the moulding composition, of other thermoplastics may be present, for example impact-modifying rubbers or polyolefins such as polyethylene or polypropylene. Any rubbers or polyolefins present preferably comprise, as known to one of skill in the art, functional groups with which compatibility with the polyamide matrix may be obtained. In addition, the assistants and additives customary for polyamides may be present, especially light and/or heat stabilizers, or preferably also light-reflecting fillers, for example titanium dioxide (WO 2011066595).

(82) The moulding composition of the layer c) may comprise either one of the abovementioned polyesters or a plurality thereof as a mixture. In addition, up to 50% by weight and preferably up to 40% by weight, based in each case on the overall polymer content of the moulding composition, of other thermoplastics may be present, for example impact-modifying rubbers or polyolefins such as polyethylene or polypropylene, or polyamine-polyamide graft copolymer. Any rubbers or polyolefins present preferably comprise functional groups to improve matrix compatibility; additionally or alternatively thereto, it may be possible to add a compatibilizer. In addition, the assistants and additives customary for polyester may be present, especially light and/or heat stabilizers, light-reflecting fillers, for example titanium dioxide, and reinforcing fillers, for example glass fibres, wollastonite or mica.

(83) For the moulding composition of the layer e), the same applies as for the moulding composition of the layer according to a), and also, with regard to fillers, the same as for the moulding composition of the layer c). In addition, the moulding composition of the layer e) may be coloured and/or have a matting agent.

(84) The individual film layers may have the following thicknesses: layers a) and e): 15 to 100 m and preferably 25 to 50 m; layer c): 100 to 500 m and preferably 150 to 400 m; layers b) and d): 3 to 40 m and preferably 5 to 25 m.

(85) The multilayer film used in accordance with the invention may be produced by all conventionally known methods, for example coextrusion or lamination. The film may be bonded to the sealing layer into which the solar cell is embedded, for example, by lamination or adhesive bonding. Due to the polyamide content in the layer a), good adhesion to the sealing layer may be obtained in the case of lamination. The sealing layer used may be any material commonly used in the art.

(86) The present invention also provides a photovoltaic module which has been produced using the multilayer film according to the embodiments and arrangements.

(87) Having generally described this invention, a further understanding can be obtained by reference to certain specific examples which are provided herein for purposes of illustration only, and are not intended to be limiting unless otherwise specified.

EXAMPLES

(88) The moulding compositions which follow were produced; parts are always parts by weight.

(89) Compound 1 for Outer Layers:

(90) 79.25 parts of VESTAMID L1901 nf (PA12), 0.5 part of IRGANOX 1098 (a sterically hindered phenolic antioxidant), 0.2 part of TINUVIN 312 (UV absorber) and 20 parts of the titanium dioxide Sachtleben R 420 were mixed with the aid of a twin-screw extruder (Coperion Werner & Pfleiderer ZSK 25 WLE, 36 L/D) at a barrel temperature of 220 C. The extrudate was cooled with the aid of a water bath and chopped; the pellets were subsequently dried in a forced-air oven at 80 C. for 12 hours.

(91) Compound 2 for Outer Layers:

(92) 69.25 parts of VESTAMID L1901 nf, 10 parts of polyamine-polyamide graft copolymer (prepared according to EP 1 065 236 A2 from 87.063% by weight of laurolactam, 0.164% by weight of dodecanedioic acid, 8.205% by weight of 50% Lupasol G 100, 0.010% by weight of 50% hypophosphorous acid and 4.558% by weight of demineralized water), 0.5 part of IRGANOX 1098, 0.2 part of TINUVIN 312 and 20 parts of the titanium dioxide Sachtleben R 420 were mixed with the aid of a twin-screw extruder (Coperion Werner & Pfleiderer ZSK 25 WLE, 36 L/D) at a barrel temperature of 220 C. The extrudate was cooled with the aid of a water bath and chopped; the pellets were subsequently dried in a forced-air oven at 80 C. for 12 hours.

(93) Compound 3 for Middle Layer:

(94) 35.5 parts of VESTAMID L1901 nf, 44.0 parts of VESTODUR 3000 (PBT), 20 parts of TEC 110 kaolin, 0.25 part of IRGAFOS 168 (processing stabilizer) and 0.25 part of IRGANOX 1010 (sterically hindered phenolic antioxidant) were mixed with the aid of a twin-screw extruder (Coperion Werner & Pfleiderer ZSK 25 WLE, 36 L/D) at a barrel temperature of 260 C. The extrudate was cooled with the aid of a water bath and chopped; the pellets were subsequently dried in a forced-air oven at 80 C. for 12 hours.

(95) Compound 4 for Middle Layer:

(96) 26.5 parts of VESTAMID L1901, 9.0 parts of the same polyamine-polyamide graft copolymer as in Compound 2, 44.0 parts of VESTODUR 3000, 20 parts of TEC 110 kaolin, 0.25 part of IRGAFOS 168 and 0.25 part of IRGANOX 1010 were mixed with the aid of a twin-screw extruder (Coperion Werner & Pfleiderer ZSK 25 WLE, 36 L/D) at a barrel temperature of 260 C. The extrudate was cooled with the aid of a water bath and chopped; the pellets were subsequently dried in a forced-air oven at 80 C. for 12 hours.

(97) Compound 5 for Adhesion Promoter Layer:

(98) 51.6 parts of VESTODUR 3000, 9.0 parts of EXXELOR VA 1803 (a maleic anhydride-functionalized ethylene-propylene rubber), 26.0 parts of VESTAMID ZA7295nf (PA12 extrusion type), 13.4 parts of the same polyamine-polyamide graft copolymer as in Compound 2, 0.25 part of IRGAFOS 168 and 0.25 part of IRGANOX 1010 were mixed with the aid of a twin-screw extruder (Coperion Werner & Pfleiderer ZSK 25 WLE, 36 L/D) at a barrel temperature of 260 C. The extrudate was cooled with the aid of a water bath and chopped; the pellets were subsequently dried in a forced-air oven at 80 C. for 12 hours.

(99) Extrusion of Multilayer Films:

(100) A multilayer film system from Collin (300 mm slot die, gap width 0-6 mm, co-extrusion feed block for 3-layer or 5-layer films) was used to produce three- and five-layer films (processing temperature for middle layer and adhesion promoter layers approx. 260 C., and for outer layers approx. 230 C.). The layer thickness distribution was set as follows: a/c/e: 50 m/250 m/50 m a/b/c/d/e: 50 m/10 m/230 m/10 m/50 m

(101) The results are shown in Table 1.

(102) TABLE-US-00001 TABLE 1 Examples Interlaminar Layer structure adhesion [N/mm] Comparative Compound 1/Compound 3/Compound 1 0.3 Example Example 1 Compound 2/Compound 3/Compound 2 Separation impossible Example 2 Compound 1/Compound 4/Compound 1 Separation impossible Example 3 Compound 1/Compound 5/Compound 3/ Separation Compound 5/Compound 1 impossible

(103) Numerous modifications and variations on the present invention are possible in light of the above description. It is therefore to be understood that within the scope of the appended claims, the invention may be practiced otherwise than as specifically described herein.