EP2040920A1

EP2040920A1 - Multilayer film

Info

Publication number: EP2040920A1
Application number: EP07785889A
Authority: EP
Inventors: Rainer Brandt; Gregor Kaschel; Esko Saaristo; Timo Toivola
Original assignee: Wipak Walsrode GmbH and Co KG
Current assignee: Wipak Walsrode GmbH and Co KG
Priority date: 2006-07-07
Filing date: 2007-07-04
Publication date: 2009-04-01
Also published as: DE102006031841A1; CA2656476A1; WO2008003471A1; US20090280278A1

Abstract

The invention relates to a multilayer film comprising a layer A which is based on a thermoplastic polymer or a mixture of several thermoplastic polymers having a melting point T<SUB>m</SUB>

Description

Multilayer film

The invention relates to a multilayer film, which is particularly suitable for the production of food packaging. Furthermore, the invention relates to a method for producing such a multilayer film.

Multilayer composites of oriented films are well suited for use as packaging materials for sensitive products. It is desirable for various reasons that the composites are printed, metallized and / or coated with a (semi-) metal oxide. For example, information can be conveyed by means of printed images, areas metallised or coated with (HalB) metal oxides contribute to the barrier effect against moisture, gases and aromas and can also have aesthetic advantages.

In order to protect the printed, metallised or (half) metal oxide coated area from external mechanical influences, it should preferably be located on the inside, i. be arranged between at least two layers of the composite.

However, multilayer films with an inner printed, metallized or (semi-) metal oxide coated region can not be produced in a single process step using conventional processes. Such composites are usually prepared by a multi-stage process, wherein initially two films are produced independently, of which at least one film is printed on its outer surface, metallized or coated with a (semi-) metal oxide. Subsequently, both films are connected by means of suitable laminating adhesives to form a multilayer film such that the printed, metallized or coated with a (half) metal oxide region between the two films is arranged. If at least one of the two films is transparent, then the printed, metallized or coated with a (half) metal oxide region can be viewed from the outside. The laminating adhesives provide a satisfactory bond between the films. At the time of application, they allow wetting of the surface of the films, in particular of the printed, metallized or coated with the (semi-) metal oxide area, and harden in the adhesive joint.

However, laminating adhesives have u.a. the disadvantage that they have to cure, which usually takes several days, sometimes up to two weeks, so that the composite can not immediately be processed as packaging material. Furthermore, the recyclability of composite films containing cured laminating adhesives is severely limited.

Depending on the packaged goods, laminating adhesives can have the disadvantage that they store color pigments. In particular, in the packaging of spices, such as curry, it is known that the pigments contained in the spice can diffuse through the individual layers of the package with time and finally reach the laminating adhesive, where they store. This leads u.a. for the packaging to appear spotted on the outside.

In addition, multilayer films containing laminating adhesives are only partially suitable for packaging perishable foods. For example, cured laminating adhesives usually contain residues of substances capable of migrating, which are harmful or even toxic and can diffuse out of the packaging into the food. Examples of such migratory substances are certain isocyanates and certain primary amines, which are typical constituents of laminating adhesives. In this connection, reference can also be made to BD Page et al., Food Addit Contam. 1992, 9 (3), 197-212; TP McNeal et al., J. AOAC Int. 1993, 76 (6), 1268-75; M. Sharman et al., Food Addit Contam. 1995, 12 (6), 779-87; Lawson, et al., Anal. Bioanal Chem. 1996, 354 (4), 483-9; G. Lawson et al., Analyst. 2000, 125 (1), 115-8; and AP liver, Chem Biol Interact. 2001, 135-136, 215-20. When adhesives cure properly, food regulations are met. However, the curing process takes a long time and requires monitoring, so this is associated with considerable financial and time. In addition, about 40% of the isocyanate-containing laminating adhesives used today contain organic solvents which are emitted in the production of composite films. Avoiding these emissions is a contribution to integrated environmental protection.

Various concepts are known in the prior art to circumvent the disadvantages of conventional laminating adhesives.

For example, laminating adhesives were developed whose content of migratory, hazardous substances after curing is lower than with conventional laminating adhesives. However, these laminating adhesives are not satisfactory in every respect. On the one hand, they are on the one hand comparatively expensive, on the other hand, the composite adhesion - depending on the material properties of the films to be joined - does not always meet the requirements imposed on the packaging material and they usually have longer curing times.

Furthermore, multilayer films have been developed which have a barrier layer which prevents the migratory components from reaching the package. For the production of such barrier layers, however, special materials must be used, whereby the production of the multilayer films is comparatively complicated and expensive.

Also, various concepts are known in the art to connect two prefabricated films without the use of laminating adhesives.

For example, EP-A 1 167 017 discloses a process in which polyethylene (PE) is melted in an extruder and applied between two BOPP films (extrusion lamination), one of which is printed on a BOPP film and the other is metallised. The BOPP films are bonded together by curing the polyethylene so that the metallized side and the ink are inside.

Although the extrusion lamination permits the avoidance of laminating adhesives, it has the disadvantage that the polymer is extruded onto a comparative Wise high temperature must be heated so that usually increased demands on the temperature resistance of printing inks and metallized films must be made and special measures are required to prevent curling of the resulting composite. Further, the high temperature of the extruded polymer melt requires that the film to be coated have sufficient temperature resistance. Thus, the polymer melt whose temperature, depending on the polymer in the range of 300 ⁰ C, must not damage the film to be coated. BOPP in particular is endangered here because it has a comparatively low melting point at approx. 164 ° C. Furthermore, printed and / or vacuum-metallized films are at risk because the hot melt is applied in direct contact. Cracks in the vacuum-applied layer, changes in print image, etc. are the result. In addition, for production reasons, the extruded layer has a certain minimum layer thickness, which is accompanied by an increased use of materials. In particular, however, the extrusion lamination has the disadvantage that the composite adhesion between the extruded layer and the two layers connected by it is relatively small. In most cases the adhesion is below 1, 0 N / 15 mm.

US 6,368,722 discloses laminated multilayer films prepared by preparing a heat-resistant polymer in a dipolar aprotic solvent, e.g. N-methyl-2-pyrrolidone is dissolved. The solution is then applied to an oriented film and dried at elevated temperature.

Although this method also works without laminating adhesives, however, the composites usually contain not insignificant residual amounts of harmful solvent. In addition, this method can not assemble surface printed films since the ink would be attacked by the solvent.

It is also known in the art to produce composites by thermal lamination. In this case, a film which has a heat-laminatable layer on one of its surfaces is usually joined to a substrate under the effect of heat and pressure. By thermal lamination can also be on The use of laminating adhesives are dispensed with, but the previously known processes are usually used for the production of composites from a plastic film and a possibly printed porous substrate made of cardboard, cardboard or paper (cf., for example, EP-A 263 882).

There is a need for multilayer films having an inner printed, metallized and / or (semi-) metal oxide coated region which completely dispense with laminating adhesives and yet have excellent composite adhesion between the assembled layers. In addition, there is a need for multilayer films having an internal printed area that can be made by processes that take little time.

The object of the invention is to provide multilayer films with an inner printed, metallized and / or (semi-) metal oxide coated region, which have advantages over the multilayer films of the prior art. The multilayer films should be suitable as packaging materials for perishable food, can be produced inexpensively and have a good adhesion between the layers in the printed, metallized or coated with a (semi) metal oxide area. The multilayer films should manage without migratable, health-endangering substances to comply with the technical requirements, in particular high barrier properties to water vapor and oxygen, and be competitive in manufacturing costs with conventional multilayer films. Furthermore, they should be able to be used as packaging materials as soon as possible after their production, i. longer cooling or curing periods should be avoided. In the most favorable case, only periods of less than one hour, preferably less than 10 minutes, should lie between the production of the multilayer film and its suitability for use on a packaging machine.

This object is solved by the subject matter of the claims.

It has surprisingly been found that multilayer films can be produced from two independently produced films, of which at least one film has on one of its outer surfaces a printed, metallized and / or coated with a (semi-) metal oxide region D, wherein excellent bond adhesion values can be achieved without the use of laminating adhesives is required.

This is particularly surprising since it was anticipated that a printed area metallized and / or coated with a (semi-) metal oxide would typically significantly degrade the composite adhesion.

Furthermore, the multilayer films of the invention have excellent sensory properties, i. are e.g. superior to many conventional multilayer films in terms of preserving the odor and taste of the packaged product.

The invention relates to a multilayer film comprising

Layer A which is based on a thermoplastic polymer or a mixture of several thermoplastic polymers having a melting temperature T _m ^A and a VICAT softening temperature T _V ^A and a layer thickness of at most 40 μm, preferably at most 35 μm, more preferably at most 30 μm, even more preferably at most 25 μm, most preferably at most 20 μm and in particular at most 15 μm; and

Layer B, which is directly adjacent to layer A, is based on a thermoplastic polymer or a mixture of several thermoplastic polymers having a melting temperature T _m ^B and a VICAT softening temperature T _V ^B and a layer thickness of at most 50 μm, preferably at most 40 μm, more preferably at most 30 μm, more preferably at most 20 μm, most preferably at most 15 μm and in particular at most 10 μm;

in which

T _V ^B <T _V ^A and T _m ^B <T _m ^A , preferably T _V ^B <T _V ^A <T _m ^B <T _m ^A or T _V ^B <T _m ^B <TA v < _τ A.

- I ¹ nmi

T _V ^B <115 ° C; preferably T _V ^B = 80 ± 35 ° C; more preferably T _V ^B = 70 ± 25 ° C, 80 ± 25 ° C or 90 ± 25 ° C; even more preferably T _V ^B = 65 ± 20 ° C, 75 ± 20 ° C, 85 ± 20 ° C or 95 ± 20 ° C; most preferably T _V ^B = 60 ± 15 ° C, 70 ± 15 ° C, 80 ± 15 ° C, 90 ± 15 ° C or 100 ± 15 ° C; and in particular T _V ^B = 55 ± 10 ° C, 60 ± 10 ° C, 65 ± 10 ° C, 70 ± 10 ° C, 75 ± 10 ° C, 80 ± 10 ° C, 85 ± 10 ° C, 90 ± 10 ° C, 95 ± 10 ° C, 100 ± 10 ° C or 105 ± 10 ° C;

preferably T _m ^B = 110 ± 35 ° C; more preferably T _m ^B = 100 ± 25 ° C, 110 ± 25 ° C or 120 ± 25 ° C; even more preferably T _m ^B = 95 ± 20 ° C, 105 ± 20 ° C, 115 ± 20 ° C or 125 ± 20 ° C; most preferably T _m ^B = 80 ± 15 ° C, 90 ± 15 ° C, 100 ± 15 ° C, 110 ± 15 ° C, 120 ± 15 ° C or 130 ± 15 ° C; and in particular T _m ^B = 85 ± 10 ° C, 90 ± 10 ° C, 95 ± 10 ° C, 100 ± 10 ° C, 105 ± 10 ° C, 110 ± 10 ° C, 115 ± 10 ° C 120 ± 10 ° C, 125 ± 10 ° C, 130 ± 10 ° C or 135 ± 10 ° C; the multilayer film comprises at least one, preferably at least two, more preferably at least three at least monoaxially, preferably biaxially oriented layer (s);

the multilayer film comprises an outer sealant layer; between layer A and layer B a printed and / or metallized and / or coated with a (half) metal oxide region D is arranged; and

the bond between layer A and layer B is at least 1.0 N / 15 mm, preferably at least 1.5 N / 15 mm, at least 2.0 N / 15 mm or at least 2.5 N / 15 mm, more preferably at least 3.0 N / 15 mm, at least 3.5 N / 15 mm or at least 4.0 N / 15 mm, more preferably at least 4.5 N / 15 mm, at least 5.0 N / 15 mm or at least 5.5 N / 15 mm, most preferably at least 6.0 N / 15 mm, at least 6.5 N / 15 mm or at least 7.0 N / 15 mm and especially at least 7.5 N / 15 mm, at least 8.0 N / 15 mm or at least 8.5 N / 15 mm, preferably determined according to DIN 53 357 method B.

Figures 1 and 2 show a template, which is preferably used to determine the curl of the multilayer film according to the invention. FIG. 3 shows schematically the curl tendency of a multilayer film in the transverse direction (left) and in the longitudinal direction (right) to the film web.

The multilayer films according to the invention are particularly suitable for packaging perishable foods, since contamination of the packaged goods by migration-capable substances can be largely excluded. The multilayer film according to the invention has, between layer A and layer B, a printed and / or metallized area D and / or area D coated with a (semi-) metal oxide. This is expressed below by the notation "ADB". Since region D is not to be regarded as an independent layer of the multilayer film, layer A directly adjoins layer B, ie there is no further layer between layer A and layer B.

The area D may cover the entire main extension plane (area) of the multilayer film or only a part thereof.

In a preferred embodiment, the region D covers the entire main plane of extension of the multilayer film. This embodiment is particularly preferred when the region D is a metallized and / or coated with a (HaIb -) metal oxide region.

In another preferred embodiment, region D covers less than the entire major plane of extent of the multilayer film, preferably less than 95%, more preferably less than 90%, even more preferably less than 85%, most preferably less than 80% and most preferably less than 50%. In this case, area D may be contiguous or divided into several subregions. This embodiment is particularly preferred when the region D is a printed and / or metallized region. If the region D is a metallized region which covers less than the entire main extension plane of the multilayer film, it is preferably a demetallized region, i. During production, the metallized area initially covered the entire main extension plane of the multilayer film, but partial removal of the metal film (demetallization) subsequently created areas which are not (anymore) metallized. Suitable processes for demetallization are known to the person skilled in the art. For example, the demetallization can be realized by means of etching techniques.

If the area D is a printed area, it may include symbols or letters. In a preferred embodiment, the distance of the curled edges of a cross-section is used as a measure of the curl (film curl) of the multilayer film according to the invention. The multilayer film according to the invention preferably has a curl of at most 50 mm in the longitudinal and / or transverse direction, more preferably at most 40 mm, even more preferably at most 30 mm, most preferably at most 20 mm and in particular at most 10 mm. Suitable methods for determining the curl of multilayer films are known to those skilled in the art. According to the invention, the tendency to curl is determined by the so-called cross-cut method. This is described in more detail in the experimental part.

Alternatively, the curl can be determined for example by the so-called. Ronde method. If the radius of curvature is used as a measure of the curl, the determination is preferably carried out according to US Pat. No. 4,565,738. The curling tendency is preferably at most 60 °, more preferably at most 50 °, even more preferably at most 40 °, most preferably at most 30 ° and in particular at most 20 °.

Layer A and layer B of the multilayer film according to the invention are each independently based on a thermoplastic polymer or a mixture of a plurality of thermoplastic polymers having a melting temperature T _m ^A and T _m ^B and a VICAT softening temperature T _V ^A and T ¹ _V V ^B.

The melting temperature of the polymer is preferably determined by DSC according to DIN ISO 11357 or ISO 3146 / ASTM D3418.

In the case of a polymer mixture, the mixture is preferably investigated in accordance with DIN ISO 11357 or ISO 3146 / ASTM D3418 and the temperature to be assigned to the main peak in the DSC is, in the context of the invention, the melting temperature of the polymer mixture.

The VICAT softening temperature (VST A / 120) of the polymer or of the polymer mixture is preferably determined in accordance with DIN EN ISO 306 / ASTM D1525. If the thermoplastic polymer has only a VICAT softening temperature, but not a melting temperature, for example because it is a completely amorphous polymer, it is true for the purposes of the invention that the melting temperature corresponds to the measured VICAT softening temperature (T _m = T _v ).

In a preferred embodiment of the multilayer film according to the invention, layer A and layer B are each based neither on a laminating adhesive nor on a lacquer. Particularly preferably, the multilayer film according to the invention comprises no laminating adhesive and / or lacquer at all.

Laminating adhesives are known to a person skilled in the art. A "laminating adhesive ^1" in the sense of the description is preferably defined as a product which due to its chemical composition and its physical state at the time of application between two layers to be joined wetting of the surface and in the adhesive joint due to physical processes (eg evaporation more volatile Solvent) and / or chemical reactions (eg formation of covalent bonds) cures.There is preferably a laminating adhesive in the dried or cured state to a thermoset.

A "laminating adhesive" in the sense of the description is preferably a chemically reacting adhesive which may be cold or thermosetting and includes polymerization, polyaddition and polycondensation adhesives Examples of one-component polymerization adhesives are cyanoacrylate adhesives (cyanoacrylates) and Examples of polyaddition adhesives are epoxy resin adhesives and polyurethane adhesives Examples of polycondensation adhesives include formaldehyde condensates, certain polyamides, certain polyesters, silicones, polyimides, polybenzimidazoles and polysulfones, these being Usually not used or only in exceptional cases as laminating adhesives.

A widespread group of Kaschierklebstoffe form the previously mentioned polyurethane adhesives, ie those products which as free functional Groups of isocyanates (-NCO) included. Its adhesive effect is sometimes based on the chemical reaction of the isocyanates with hydroxyl groups or other suitable functional groups, which are available on the surface of the layer to be bonded. In this way, there is a covalent bond between the laminating adhesive and the layers, for example via urethane groups (-O-CO-NH-). Also, laminating adhesives based on (meth) acrylate are quite common. Other functional groups which may be involved in the curing of laminating adhesives are: -NH ₂ , -CO ₂ H, -CHO, -CN, -SH, -Cl, -CH = CH ₂ , -CH ₂ CH = CH ₂ and epoxy.

On the one hand, a distinction is made between single-component and multi-component systems and, on the other hand, between laminating adhesives based on aliphatic and / or aromatic building blocks. Furthermore, a distinction is made between solvent-based and solvent-free laminating adhesives. For further details, reference may be made in full, for example, to G. Habenicht, Glue: Grundlagen, Technologie, Anwendungen, Springer Verlag, 1986. Laminating adhesives are typically applied in thicknesses greater than 0.5 μm for practical reasons.

A person skilled in the art knows about coatings. A "paint" in the sense of the description is preferably defined as a liquid which forms a solid, stable, usually glossy layer after drying and thus protects the surface provided therewith and optionally decorates. It is preferably a product which due to its chemical composition and its physical state at the time of application on a layer wetting of the surface allows and due to physical processes (eg evaporation of volatile solvents) and / or chemical reactions (eg formation of covalent bonds ) hardens.

The multi-layer film according to the invention preferably contains - in addition to the possibly existing printing inks in the printed area D - no lacquer. In particular, the multilayer film according to the invention particularly preferably contains, in addition to the printing inks, no further substance or composition which, due to chemical processes and / or by evaporation of a solvent, is used in the production of the multilayer film. was hardened. This has the advantage, inter alia, that the multilayer film according to the invention is better recyclable and suitable for the packaging of foods.

In a preferred embodiment, the multilayer film according to the invention comprises eight, seven, six, five, four, three or only two layers. In the latter case, the multilayer film consists of layer A and layer B, so that at least layer A or layer B is at least monoaxially stretched and at least layer A or layer B forms an outer sealing layer of the multilayer film.

In a preferred embodiment, the multilayer film according to the invention has a total layer thickness of at most 200 μm, at most 190 μm or at most 180 μm; more preferably at most 170 μm, at most 160 μm or at most 150 μm; even more preferably at most 140 μm, at most 130 μm or at most 120 μm; most preferably at most 110 μm, at most 100 μm or at most 90 μm; and in particular at most 80 μm, at most 70 μm or at most 60 μm.

The multilayer film according to the invention is preferably not thermoformable, in particular not deep drawable.

Layer A and / or layer B of the film according to the invention is preferably transparent. A "transparent layer" in the sense of the invention is characterized in that a packaged product can be viewed through this layer with the naked eye.

The transparency is preferably quantified with the aid of densitometers. Such methods are familiar to the person skilled in the art. Preferably, as a measure of the transparency, the turbidity can be measured as an optical value. The turbidity is preferably measured according to the ASTM test standard D 1003-61 m, Procedure A, after calibration of the measuring instrument with turbidity standards between 0.3 and 34% haze. By way of example, a Byk-Gardner Hazemeter with Ulbricht sphere, which allows integrated measurement of the diffuse light transmittances at a solid angle of 8 ° to 160 °, is suitable as a measuring instrument. The individual layers of the multilayer film of the invention when unprinted preferably have a haze determined by the method described above of less than 14%, more preferably less than 12%, even more preferably less than 10%, most preferably less than 8% and especially less than 6%. on.

As such, the multilayer film as such has a haze of less than 30%, more preferably less than 25%, even more preferably less than 20%, most preferably less than 15% and in particular less than 10%, at least in optionally unprinted areas.

In a preferred embodiment, starting from region D, all layers optionally on the side of layer A, including layer A, have a total haze of less than 30%, more preferably less than 28%, even more preferably less than 26%, most preferably less than 24% and especially less than 22%. In another preferred embodiment, starting from region D, all layers possibly including the layer B side, including layer B, have an overall haze of less than 30%, more preferably less than 28%, even more preferably less than 26% most preferably less than 24% and in particular less than 22%.

The multilayer film according to the invention comprises at least one at least monoaxially, preferably biaxially oriented layer. This may be layer A, layer B or a possibly existing layer other than layer A and layer B.

The orientation of polymers by stretching a film is familiar to the person skilled in the art. If thermoplastic polymers are stretched at temperatures at which the molecules can still slide along one another, but the relaxation times are much greater than the time during which they are kept at elevated temperature for the drawing process, the orientation achieved in the course of stretching remains. ie the orientation of the polymer strands in the direction of stretching. The stretching results in significant property changes in both amorphous and partially crystalline thermoplastic polymers. mers. A biaxial stretching preferably takes place in the machine direction and transversely thereto, wherein the stretching can take place simultaneously or sequentially. The area stretching ratio is preferably in the range of 5 to 60, more preferably 7 to 55, still more preferably 9 to 50, and especially 9 ± 2, 20 ± 5 or 50 ± 10.

In one embodiment of the multilayer film according to the invention, layer A and / or layer B forms a surface of the multilayer film according to the invention.

Preferably, the total layer thickness is independent of each other

- Of layer A and all possibly on the side of layer A, which layer B is remote, arranged layers and / or

layers arranged in the range of 5.0 to 100 μm, more preferably 7.5 to 75 μm, more preferably 10 μm to 50 μm, of layer B and all, if appropriate, on the side of layer B which faces away from layer A, on most preferably 10 μm to 40 μm and in particular 15 μm to 30 μm.

Layer A of the multilayer film according to the invention is based on a polymer or a polymer mixture having a melting temperature T _m ^A. Preferably 70 ⁰ C ≦ T _m ^A <260 ⁰ C, more preferably 80 ° C <T _m ^A <240 ° C, even more preferably 90 ° C <T _m ^A <220 ° C, most preferably 100 ⁰ C <T _m ^A <200 ° C and in particular 110 ° C <T _m ^A <180 ° C.

The melt flow index of the polymers or of the mixture of the polymers on which layer A is based (MFI ^A , ISO 1133 / ASTM D1238, 2.16 kg / 10 min) is preferably in the range from 0.3 to 9.5 g / 10 min; more preferably 3.5 ± 2.0 g / 10 min, 5.5 ± 2.0 g / 10 min or 7.5 ± 2.0 g / 10 min; more preferably 3.0 ± 1.5 g / 10 min, 4.0 ± 1.5 g / 10 min, 5.0 ± 1.5 g / 10 min, 6.0 ± 1.5 g / 10 min, 7.0 ± 1.5 g / 10 min or 8.0 ± 1.5 g / 10 min; most preferably 2.5 ± 1, 0 g / 10 min, 3.5 ± 1, 0 g / 10 min, 4.5 ± 1, 0 g / 10 min, 5.5 ± 1, 0 g / 10 min, 6.5 ± 1, 0 g / 10 min, 7.5 ± 1, 0 g / 10 min or 8.5 ± 1, 0 g / 10 min; especially 1, 0 ± 0.5 g / 10 min, 1, 5 ± 0.5 g / 10 min, 2.0 ± 0.5 g / 10 min, 2.5 ± 0.5 g / 10 min, 3 , 0 ± 0.5 g / 10 min, 3.5 ± 0.5 g / 10 min, 4.0 ± 0.5 g / 10 min, 4.5 ± 0.5 g / 10 min, 5.0 ± 0.5 g / 10 min, 5.5 ± 0.5 g / 10 min, 6.0 ± 0.5 g / 10 min, 6.5 ± 0.5 g / 10 min, 7.0 ± 0 , 5 g / 10 min, 7.5 ± 0.5 g / 10 min, 8.0 ± 0.5 g / 10 min, 8.5 ± 0.5 g / 10 min or 9.0 ± 0.5 g / 10 min. For polyethylene and ethylene Copolymers, the melt flow index is usually measured at 190 ⁰ C, in polypropylene and propylene copolymers usually at 230 ⁰ C.

The viscosity number of the polymers or of the mixture of the polymers on which layer A is based (determined according to ISO 307, solution 0.005 g / ml H ₂ SO ₄ ) is preferably in the range of 190 ± 75 ml / g, more preferably 190 ± 50 ml / g, more preferably 190 ± 30 and especially 190 ± 10 g / ml.

The intrinsic viscosity of the polymers or the mixture of polymers on which layer A is based (v _int ^A determined according to DIN 51562-3) is preferably in the range of 0.8 ± 0.3 dl / g, more preferably 0.8 ± 0.2 dl / g and in particular 0.8 ± 0.1 dl / g.

In a preferred embodiment, the density p ^{A of} the polymers or the mixture of the polymers on which layer A is based (ISO 1183 / ASTM D792) is in the range of> 1.00 g cm ^-3 , more preferably> 1.10 g cm ^"3 , more preferably ≥1.15 g cm ^{" 3} , most preferably ≥1.20 g cm ^"3, and in particular ≥1.25 g cm- ³ . In another preferred embodiment, the density ρ ^{A of} the polymers is Mixture of the polymers on which layer A is based (ISO 1183 / ASTM D792), in the range of <1, 00 g cm ^"3 , more preferably <0.98 g cm ^'3 , even more preferably <0.96 g cm ^{" 3} , most preferably <0.94 g cm ^-3 and in particular ≤ 0.92 g cm ^-3 .

Layer A is preferably based on at least one polymer selected from the group consisting of (co) polyolefins, (co) polyesters, (co) polycarbonates and (co) polyamides. For purposes of description, the term "(co) polyolefin" includes both polyolefins and copolyolefins. Accordingly, the term "(co) polyester" includes both polyesters and copolyesters, the term "(co) polycarbonates" includes both polyacrolates and copolycarbonates and the term "(co) polyamides" includes both polyamides and copolyamides ,

Preferred (co) polyolefins according to the invention are selected from the group consisting of PE (in particular LDPE ₁ LLDPE, HDPE or mPE), PP, PI ₁ PB, EAA, EMAA ₁ EVA, EPC, PMMA, I ₁ PS, SEP ₁ SEPS, SEBS, SEEPS and thermoplastic elastomers or their copolymers. By "PE" is meant polyethylene, with "PP" polypropylene. By "LDPE" is meant low density polyethylene which has a density in the range of 0.86-0.93 g / cm ³ and is characterized by a high degree of branching of the molecules. A sub-form of LDPE forms linear low-density polyethylene (LLDPE), which in addition to ethylene as comonomer one or more α-olefins having more than 3 carbon atoms, for example, but-1-ene, hex-1-ene, 4-methyl-pentene 1-en and Oct-1-ene. The copolymerization of the monomers mentioned gives the typical LLDPE molecular structure, which is characterized by a linear main chain with side chains located thereon. The density varies between 0.86 and 0.94 g / cm ³ . The melt flow index MFR of polyethylene-based polymers is preferably between 0.3 and 15 g / 10 min (at 190 ° C / 2.16 kg load, measured according to DIN EN ISO 1133). The melt flow index MFR of polypropylene-based polymers is preferably between 0.3 and 30 g / 10 min (at 230 ° C / 2.16 kg load, measured according to DIN EN ISO 1133). By "HDPE" is meant high density polyethylene which has little branching of the molecular chain, the density may range between 0.94 and 0.97 g / cm ³ . By "mPE" is meant an ethylene copolymer which has been polymerized by means of metallocene catalysts. As the comonomer, an α-olefin having 4 or more carbon atoms is preferably used. The density is preferably between 0.88 and 0.93 g / cm ³ . The dispersity M _w / M _n is preferably less than 3.5, preferably less than 3.0.

"PI" is polyisobutylene, "PB" polybutylene.

"EAA" denotes copolymers of ethylene and acrylic acid and "EMAA" copolymers of ethylene and methacrylic acid. The ethylene content is in each case preferably between 60 and 99 mol%.

By "EVA" is meant a copolymer of ethylene and vinyl acetate. The ethylene content is preferably between 60 and 99 mol .-%.

As "EPC" are ethylene-propylene copolymers with 1-10 mol .-% of ethylene, wherein the ethylene is randomly distributed in the molecule. By "PMMA" is meant polymethylmethacrylate and its copolymers.

"I" refers to olefins based copolymers whose molecules are crosslinked via ionic bonds (ionomers). The ionic bond is reversible, which causes a dissolution of the ionic bond at ordinary processing temperatures (about 180-290 ⁰ C) and a reformation of the ionic bond in the cooling phase. Typically, copolymers of ethylene polymers as employed with acrylic acids, which are crosslinked by sodium or zinc ions such as Surlyn ^®

"PS" refers to polystyrenes and styrene copolymers. An examples of a styrene copolymer is styrene-butadiene copolymer, for example, Styroflex ^®.

"SEP" is hydrogenated polyC-styrene-b-isoprene J-block copolymers, "SEPS" hydrogenated polyC-styrene-b-isoprene-b-StyroO-block copolymers, "SEBS" hydrogenated polyC-styrene-b-butadiene-b-styrene. Block copolymers and "SEEPS" hydrogenated poly (styrene-b-isoprene / butadiene-b-styrene) block copolymers called. They are obtainable for example under the name SEPTON ^®.

Examples of "thermoplastic elastomers" are styrene-vinyl-polyisoprene (block -) - copolymers, for example HYBRAR ^®. They include blocks of polystyrene, vinyl-polyisoprene, polyisoprene, hydrogenated vinyl-polyisoprene and hydrogenated polyisoprene.

Preferred (co) polyesters according to the invention are selected from the group consisting of PET (in particular c-PET or a-PET), CoPET ₁ PBT and CoPBT. By "PET" is meant polyethylene terephthalate, which can be prepared from ethylene glycol and terephthalic acid. Furthermore, a distinction can be made between amorphous PET (a-PET) and crystalline PET (c-PET). "CoPET" refers to copolyesters which, in addition to ethylene glycol and terephthalic acid, also contain other monomers, such as, for example, branched or aromatic diol glycols. "PBT" refers to polybutylene terephthalate and "CoPBT" to a copolyester of polybutylene terephthalate. PBT can be prepared from butane-1, 4-diol and terephthalic acid. be presented. Preferably, the polyester or copolyester has an intrinsic viscosity of from 0.1 to 2.0 dl / g, more preferably from 0.2 to 1.7 dl / g, even more preferably from 0.3 to 1.5 dl / g, most preferably 0, 4 to 1, 2 dl / g and in particular 0.6 to 1, 0 dl / g. Methods for determining the intrinsic viscosity are known to the person skilled in the art. A detailed description of PET, PBT, polycarbonates (PC) and copolycarbonates (CoPC) can be found in Kunststoffhandbuch Volume 3/1 - engineering thermoplastics: polycarbonates, polyacetals, polyesters, cellulose esters; Carl Hanser Verlag, 1992, the contents of which are fully incorporated by reference.

Preferred (co) polyamides according to the invention are aliphatic or (partially) aromatic. Preferably, the polyamide is aliphatic. Preferably, the polyamide or copolyamide has a melting point in the range of 160 to 240 ⁰ C, more preferably 170 to 222 ° C. The polyamide or copolyamide is preferably selected from the group consisting of PA 4, PA 6, PA 7, PA 8, PA 9, PA 10, PA 11, PA 12, PA 4,2, PA 4,6, PA 6,6 , PA 6.8, PA 6.9, PA 6.10, PA 6.12, PA 7.7, PA 8.8, PA 9.9, PA 10.9, PA 12.12, PA 6/6 , 6, PA 6,6 / 6, PA 6,2 / 6,2, and PA 6,6 / 6,9 / 6. PA 6 is particularly preferred. A detailed description of PA and CoPA can be found in Kunststoff-Handbuch Volume VI, Polyamides, Carl Hanser Verlag Munich, 1966; and Melvin I. Kohan, Nylon Plastics Handbook, Carl Hanser Verlag Munich, 1995, the contents of which are fully incorporated by reference.

The multilayer film of the invention has an outer sealant layer. This may be layer A, layer B or a possibly existing layer other than layer A and layer B. When the term "sealing layer S" is used for the purpose of the description, the sealing layer is a layer other than layer A and layer B. For example, the notation "S // ADB" represents a multilayer film in which the sealant layer S is disposed on the side of the layer A, which layer B faces away. In this case, "//" does not necessarily mean that the sealing layer S touches the layer A. Rather, it is also possible that one or more intermediate layers are arranged between the sealing layer S and the layer A. If only the expression "sealing layer" is used for the purposes of the description, then the sealing layer can also be identical to layer A or layer B. The sealing layer of the multilayer film according to the invention is sealable, preferably heat-sealable. The sealing layer is primarily used for welding the film. In tubular bag packaging, the sealing medium must be able to be sealed against itself, in packaging from the lid and lower shell, the sealing medium must be sealed against another sealing film. The sealing process is described, for example, in Hernandez / Selke / Culter: Plastics Packaging, Carl Hanser Verlag, Munich, 2000. The sealing layer may be peelable.

According to the invention, the sealing layer is preferably based on at least one (co) -polyolefin. The polymers used to make the sealant layer are allowed to make layers that come in contact with food. In a preferred embodiment, the sealant layer is based on at least one polyolefin selected from the group consisting of mPE, HDPE, LDPE, LLDPE, EVA, EAA, I (preferably Surlyn ^®, for example with zinc ions), PP, preferably homo-PP, and propylene Copolymerizat, or their mixture. The sealing temperatures are preferably in the range of 100 ⁰ C to 164 ° C. The melting temperature of the sealing layer is preferably from 90 ⁰ C to 164 ° C, more preferably 95 ° C to 13O ⁰ C. The sealant layer may be provided with conventional excipients such as antistatic agents, lubricants, slip agents, antiblocking agents, antifogging agents and / or spacers.

In a preferred embodiment of the multilayer film according to the invention, a printed region D is arranged between layer A and layer B. For this purpose, layer B may be printed on the side A facing the layer A and / or layer A on the side facing the layer B.

The printed area is preferably based on conventional printing inks. "Printing inks" in the sense of the description are preferably colored liquids or pastes with which a print carrier or a printing form can transfer a printed image, ie a print, reproducibly onto a substrate, ie onto at least one layer of the multilayer film according to the invention. Printing inks usually consist of binders, colorants (pigments, dyes), solvents and additives. The binders usually serve two purposes - on the one hand they wet and envelop the coloring component and transfer it to the substrate via the inking unit and the printing form - on the other hand they fix the pigments on the substrate and produce a resistant print. Typical binders are: a) semisynthetic polymers (modified natural products), for example cellulose derivatives such as nitrocellulose, ethylcellulose, cellulose acetate propionate or butyrate; and b) Fully synthetic polymers: petroleum based products, polyvinyl butyral resins (PVB), polyvinyl chloride copolymers (based on PVC), polyacrylates, polyamides, polyurethanes (PUR).

Colorants include all colorants, such as pigments, dyes and pigment preparations. Dyes are soluble substances in the application medium, pigments are practically insoluble in the application medium.

The application medium is composed of binder and solvent and optionally conventional additives. Typical solvents are organic, e.g. Ethanol, ethyl acetate, acetone, propanol, methyl ethyl ketone, etc. Additives modify the property profile of the ink, e.g. the adhesion, the elasticity and the sliding properties.

It is also possible to use solventless inks that generally cure by radiation-induced crosslinking (e.g., UV rays or electron beams).

In a preferred embodiment of the multilayer film according to the invention, a metallized region D is arranged between layer A and layer B. For this purpose, layer B may be metallized on the side A facing the layer A and / or layer A on the side facing the layer B, wherein the metallization may be over the whole area or possibly cover only a part of the main extension plane of the multilayer film.

Metallization processes are known to the person skilled in the art. In this case, usually a polymer layer is vacuum-coated with a metal, for example with aluminum. The metal settles on the polymer, forming a thin film. For example, a prefabricated polymer film may be placed in a vacuum chamber and a vacuum in the range of 10 ^"4 to 10 ^'5 bar may be generated by suitable pumps The metal, for example aluminum, is then heated to a temperature in the range of 1400 to 1500 ^° C In this way, a very thin layer of metal deposits on the surface of the polymer film, preferentially metallizing the entire surface of the polymer film: temperature, vacuum, geometry of the vacuum chamber and the speed of the polymer film through the metal vapor can be varied, whereby the thickness of the metal film can be adjusted The thickness of the metal film can be measured both electrically and optically.

In a preferred embodiment of the multilayer film according to the invention, a region D coated with a (semi-) metal oxide is arranged between layer A and layer B. For the purposes of the description, the term "(Hal) metal oxide" includes both half metal oxides (eg SiO _x ) and metal oxides (eg AlO _x ). For this purpose, layer B on the side A facing the layer A and / or layer A on the side facing the layer B may be coated with a (semi-) metal oxide.

The (semi-) metal oxide is preferably AIO _x or SiO _x . The coating can be carried out, for example, by chemical vapor deposition (CVD) or physical vapor deposition (PVD). Such methods are known to the person skilled in the art. For example, it is possible to evaporate aluminum in vacuo and deposit by metering a certain amount of oxygen AIO _x . In the case of silicon, the evaporation can take place with the aid of an electron beam. For further details, reference may be made, for example, fully to US 5,728,224.

The region D of the multilayer film according to the invention can be treated on one side with a primer. Primers are substances which are applied as a comparatively thin film, usually less than 0.05 μm, and modify the surface properties of the substrate. They differ, inter alia, in the thickness of their order of laminating adhesives, which are usually applied because of their viscosity in thicknesses of more than 0.5 microns. In contrast to Primers can be applied as a monomolecular film. A primer can be defined as a surface coating that aids adhesion to a substrate. Primers may have reactive functional groups that can react with functional groups of the polymers. A possibly present primer is not to be regarded as an independent layer, so that in this case as well layer A directly adjoins layer B, ie there is no further layer between layer A and layer B.

In a preferred embodiment, layer B has a layer thickness of at most 50%, more preferably at most 40%, even more preferably at most 30%, most preferably at most 20%, and most preferably at most 10% of the total layer thickness of layer B and all on the side of layer B ₁ Layer A is remote, arranged on layers. For example, if the multilayer film has the structure ADB // C, the layer thickness of the layer B is at most the percentage of the sum of the layer B and the layer C mentioned above.

Preferably, layer B is based on a polymer or polymer blend having a melt flow index MFI ^B (ISO 1133 / ASTM D1238, 2.16 kg / 10 min) in the range of 0.3 to 6.0 g / 10 min; more preferably 2.5 ± 1, 0 g / 10 min, 3.5 ± 1, 0 g / 10 min or 4.5 ± 1, 0 g / 10 min; more preferably 1, 5 ± 0.5 g / 10 min, 2.0 ± 0.5 g / 10 min, 2.5 ± 0.5 g / 10 min, 3.0 ± 0.5 g / 10 min, 3.5 ± 0.5 g / 10 min, 4.0 ± 0.5 g / 10 min, 4.5 ± 0.5 g / 10 min or 5.0 ± 0.5 g / 10 min. In the case of polyethylene and ethylene copolymers, the melt flow index is usually measured at 190 ^° C., in the case of polypropylenes and propylene copolymers usually at 230 ^° C.

In a preferred embodiment, MFI ^A > MFI ^B. In another preferred embodiment, MFI ^A <MFI ^B.

Preferably, layer B is based on a polymer or polymer blend having a density p ^B (ISO 1183 / ASTM D792) in the range of 0.95 ± 0.10 g cm ^'3 , more preferably 0.90 ± 0.05 g cm ^{' 3} , 0.95 ± 0.05 g cm ^-3 or 1.00 ± 0.05 g cm ^-3 ; more preferably 0.935 ± 0.025 g cm ^-3 , more preferably 0.930 ± 0.020 g cm ^-3 or 0.940 ± 0.020 g cm ^-3 ; more preferably 0.925 ± 0.015 g cm ^-3 , 0.935 ± 0.015 g cm ^-3 or 0.945 ± 0.015 g cm ^-3 ; most preferably 0.920 ± 0.010 g cm ^-3 , 0.930 ± 0.010 g cm ^-3 , 0.940 ± 0.010 g cm ^-3 or 0.950 ± 0.010 g cm ^-3 and in particular 0.920 ± 0.005 g cm ^-3 , 0.925 ± 0.005 g cm ^-3 , 0.930 ± 0.005 g cm ^"3 , 0.935 ± 0.005 g cm ^{" 3} , 0.940 ± 0.005 g cm ^{* 3} , 0.945 ± 0.005 g cm ^"3 or 0.950 ± 0.005 g cm ^{" 3} .

In a preferred embodiment, p ^A > ρ ^B. In another preferred embodiment, p ^A <ρ ^B.

In a preferred embodiment, layer B is based on at least one (co) polyolefin, preferably on a polyethylene, ethylene copolymer, polypropylene, propylene copolymer, polystyrene, styrene copolymer, polybutene, butene copolymer, polyisoprene, isoprene copolymer or the like mixtures. Ethylene copolymers are preferred, wherein they are particularly preferably selected from the group consisting of ethylene-alkyl acrylate copolymer, ethylene-vinyl acetate copolymer, ethylene-maleic anhydride copolymer and ethylene-alkylacrylate-maleic anhydride copolymer.

If layer B is based on an ethylene-alkyl acrylate copolymer, the alkyl acrylate is preferably methyl acrylate, ethyl acrylate or butyl acrylate. The proportion of the alkyl acrylate is preferably in the range of 10 to 40 mol%, more preferably 15 to 35 mol%, even more preferably 20 to 30 mol%. An example of a suitable ethylene-methacrylate copolymer is Elvaloy ^® monitor AC1224, having a density of 0.944 g cm ^"3 and a melt flow index of 2 g / 10 min and contains a proportion of 24 mol .-% of methyl acrylate.

When layer B is based on an ethylene-vinyl acetate copolymer, the proportion of the vinyl acetate is preferably in the range of 10 to 40 mol%, more preferably 15 to 35 mol%, even more preferably 20 to 30 mol%. An example of a suitable ethylene-vinyl acetate copolymer is ELVAX ^® 3190LG ₁ having a density of 0.950 g cm ^"3 and a melt flow index of 2 g / 10 min and contains a proportion of 25% of vinyl acetate mol.-.

If layer B is based on an ethylene / maleic anhydride copolymer, it is preferably a linear polyisocyanate modified with maleic anhydride. low density ethylene (LLDPE). The proportion of the maleic anhydride is preferably in the range of 0.5 to 5.0 mol%, more preferably 1.0 to 4.5 mol%, even more preferably 1.5 to 4.0 mol%. An example of a suitable ethylene-maleic anhydride copolymer is Bynel ^® 4157N, having a density of 0.920 g cm ^"3 and a melt flow index of 3 g / 10 min.

If layer B is based on an ethylene-alkyl acrylate-maleic anhydride copolymer, the alkyl acrylate is preferably methyl acrylate, ethyl acrylate or butyl acrylate. The proportion of the alkyl acrylate is preferably in the range of 1.0 to 20 mol%, more preferably 2.0 to 15 mol%, even more preferably 3.0 to 10 mol%, and the proportion of the maleic anhydride is preferably in the range from 1.0 to 10 mol%, more preferably 1.5 to 7.5 mol%, even more preferably 2.0 to 5.0 mol%. An example of a suitable ethylene-alkyl acrylate-maleic anhydride copolymer is Lotader ^® 3210, which has a density of 0.930 g cm ^"3 and a melt flow index of 5 g / 10 min, a content of 6.0 mol .-% of butyl acrylate and Contains 3.0 mol .-% maleic anhydride.

In a preferred embodiment of the multilayer film according to the invention, on the side of layer B _1, which layer A faces away, a layer C which is based on a thermoplastic polymer is arranged. Accordingly, the multilayer film according to the invention preferably has the layer sequence ADB // C. Layer C is preferably at least monoaxial, preferably biaxially oriented and / or transparent. Preferably, layer C forms an outer surface of the multilayer film.

Layer C preferably has a layer thickness in the range of 5.0 to 150 μm, more preferably 7.5 to 125 μm, even more preferably 10 to 100 μm, most preferably 12.5 to 75 μm and in particular 15 to 50 μm.

Layer C is preferably based on at least one (co) polyolefin, preferably on polyethylene, ethylene copolymer, polypropylene, propylene copolymer, polystyrene, styrene copolymer or mixtures thereof. Layer C is preferably based on a polymer or polymer blend having a density p ^c in the range 0.90 to 1.20 g cm ^-3 . In a preferred embodiment, p ^c > p ^B. In another preferred embodiment, p ^c < p ^B. More preferably, layer C is based on polyethylene, preferably low density polyethylene (LDPE) _1, ie, a density in the range of 0.915 to 0.935 g cm ^-3 . More preferably, the density is in the range of 0.920 to 0.935 g cm ^-3 , more preferably 0.925 to 0.935 g cm ^"3 and in particular 0.930 to 0.935 g cm ^{" 3} and a melt flow index MFI ^C. The melt flow index MFI ^C is preferably in the range from 1.5 to 4.5 g / 10 min, more preferably 2.0 to 4.0 g / 10 min and in particular 2.5 to 3.5 g / 10 min. A suitable LDPE is, for example, ExxonMobil LD 151 ^®, which has a density of 0.9335 g cm ^"1 and a melt flow index of 3 g / 10 min.

Layer C is preferably based on a (co) polyolefin or a mixture of several (co) polyolefins having a melting temperature T _m ^c and a VICAT softening temperature T _v ^c , where T _m ^c > T _m ^B and / or T _v ^c > T _V ^B , preferably T _m ^c > T _m ^B > T _v ^c ≥ T _V ^B or T _m ^c > T _v ^c > T _m ^B > T _v ^B.

In a preferred embodiment, MFI is ^C > MFI ^B. In another preferred embodiment, MFI ^C <MFI ^B.

In a preferred embodiment of the multilayer film according to the invention, both p ^B and p ^{c are} in the range of 0.935 ± 0.015 g cm ^-3 and MFI ^C > MFI ^B or MFI ^B > MFI ^C , preferably both MFI ^B and MFI ^{C being} in the range of 2.5 ± 1.5 g / 10 min, more preferably 2.5 ± 1.0 g / 10 min, more preferably 2.5 ± 0.5 g / 10 min.

Between layer B and the optionally present layer C of the multilayer film according to the invention, one or more intermediate layers may be arranged. Preferably, however, layer C directly adjoins layer B.

In addition to layer A, layer B, the sealing layer and the optionally present layer C, the multilayer film according to the invention can have one or more further layers, which can form intermediate or outer layers of the multilayer film. The further layers which may be present are preferably based, identically or differently, on thermoplastic polymers selected from (co) polyolefins, (co) polyesters and (co) polyamides. The polymers may optionally be foamed. In a preferred embodiment, the multilayer film according to the invention has a barrier layer BA, which is preferably gas- and / or aroma-tight. The barrier layer BA can also provide protection against moisture and / or prevent the migration of low molecular weight constituents of the multilayer film into the packaged goods. The gas-tightness of the multilayer film according to the invention, determined according to DIN 53380, is preferably less than 50, more preferably less than 40, more preferably less than 25 and in particular less than 10 [cm ³ / m ² dbar O ₂ ] at 23 ° C. and 0%. rel. Humidity.

The optionally present barrier layer BA is preferably based on at least one polymer selected from the group comprising ethylene-vinyl alcohol copolymer (EVOH); Polyvinylidene chloride (PVDC); Vinylidene chloride copolymer, preferably with a proportion of vinylidene chloride of 80% or more, preferably Saran ^® , possibly also as a blend with other polymers, such as EVA; Polyester and polyamide; preferably on ethylene-vinyl alcohol copolymer. The optionally present barrier layer BA preferably has a thickness of 0.5 to 15 μm, more preferably 1.0 to 10 μm, more preferably 1.5 to 9 μm, most preferably 2.0 to 8 μm and in particular 2.5 up to 7.5 μm.

The barrier layer BA is preferably embedded in two adhesion promoter layers HVi and HV ₂ and / or two polyamide layers PAi and PA ₂ . Thus, in addition to layer A, layer B, optionally layer C and possibly the sealing layer S, the multilayer film according to the invention preferably comprises the following layers in the following sequence:

- If necessary, a bonding agent layer HVi;

- If necessary, a polyamide PAi;

- A gas and / or aroma-dense barrier layer BA;

- If necessary, a polyamide layer PA ₂ ; and

- If necessary, a bonding agent HV ₂ .

Adhesion promoters (HV) are coextrudable, adhesion-promoting polymers. Preference is given to modified polyolefins, such as, for example, LDPE, LLDPE, mPE, EVA, EAA, EMAA, (co) PP, EPC, which are reacted with at least one monomer from the group of .alpha.,. Beta.-monounsaturated dicarboxylic acids, such as, for example, maleic acid, Fumaric acid, itaconic acid, or their anhydrides, esters, amides or imides, are grafted. In addition, copolymers of ethylene with α, ß-mono-unsaturated monocarboxylic acids such as acrylic acid, methacrylic acid and / or their metal salts with zinc or sodium and / or CrC can ₄ alkyl esters are used, wherein in addition also at least one monomer from the group α, ß-monounsaturated dicarboxylic acids, such as maleic acid, fumaric acid, itaconic acid, or their anhydrides, esters, amides or imides, can be grafted. It is also possible to use polyolefins such as, for example, PE, PP, ethylene / propylene copolymers or ethylene / α-olefin copolymers which have been copolymerized with ethylene with α, β-monounsaturated monocarboxylic acids, such as acrylic acid, methacrylic acid and / or their metal salts are grafted with zinc or sodium and / or their Ci-C ₄ -alkyl esters. Polyolefins, in particular ethylene / .alpha.-olefin copolymers with grafted .alpha.,. Beta.-monounsaturated dicarboxylic anhydride, in particular maleic anhydride, are particularly suitable as adhesion promoters. The adhesion promoters may also contain an ethylene / vinyl acetate copolymer (EVA), preferably having a vinyl acetate content of at least 10% by weight.

The optionally present adhesion promoter layer (s) H 1 and HV ₂ preferably have, identically or differently, a thickness of 0.1 to 25 μm, more preferably 0.2 to 15 μm, even more preferably 0.5 to 10 microns, most preferably 1, 0 to 7.5 microns and in particular from 2.0 to 5.0 microns.

The optionally present polyamide layer (s) PAi and PA ₂ are preferably based on the polyamides listed above in connection with the layers A and preferably have the same or different thicknesses of 0.1 to 25 μm, more preferably from 0.2 to 15 μm, more preferably from 0.5 to 10 μm, most preferably from 1.0 to 7.5 μm, and most preferably from 2.0 to 5.0 μm.

The multilayer film according to the invention preferably has the layer sequence S // AD-B // C, wherein in particular between the sealing layer S and layer A one, two, three or four additional intermediate layers can be arranged. This is expressed for the purpose of description by the sign "//". Preferred layer sequences of the multilayer film according to the invention are shown below, it being possible for further, unspecified (intermediate) layers to be present in each case:

- A-D-B;

- A-D-B // C, S // A-D-B;

- A-D-B // C // S, S // A-D-B // C;

- AD-ByZHV ₁ ZZBAZHV ₂ ZZS, SZZHV ₁ ZZBAyZHV ₂ ZZA-DB, AD-BZZPA ₁ ZZBAZZPA ₂ ZZS, SZZPA ₁ ZZBAZZPA ₂ ZZA-DB;

- AD-BZZCZZHV ₁ ZZBAZZHV ₂ ZZS, SZZHV ₁ ZZBAZHV ₂ ZZA-D-BZZC, AD-BZZCZZPA ₁ ZZBAZZPA ₂ ZZS ₁ SZZPA ₁ ZZBAZZPA ₂ ZZA-D-BZZC;

- AD-BZZHV ₁ ZZPA ₁ ZZBAZZPA ₂ ZZHV ₂ ZZS ₁ SZZHV ₁ ZZPA ₁ ZZBAZZPA ₂ ZZHV ₂ ZZA-DB;

- AD-BZZCZZHV ₁ ZZPA ₁ ZZBAZZPA ₂ ZZHV ₂ ZZS or SZZHV ₁ ZZPA ₁ ZZBAZZPA ₂ ZZHV ₂ ZZA-D-BZZC.

Particularly preferred embodiments of the multilayer film according to the invention are summarized in the following table, wherein the layer thickness of the individual layers preferably lies within the stated ranges (all values in μm) and, if appropriate, further unspecified (intermediate) layers may be present:

The individual layers of the multilayer film according to the invention may contain customary amounts of customary auxiliaries, such as pigments, lubricants, spacers, antifogging agents, etc.

Another object of the invention relates to a method for producing the multilayer film described above

(I) a film 1 comprising layer A, which forms at least one of the two surfaces of the film 1 and on at least part of this surface has a printed and / or metallized and / or coated with a (semi-) metal oxide region D;

and

(ii) a film 2 comprising layer B, which forms at least one of the two surfaces of the film 2, this surface optionally being treated with a corona discharge;

wherein film 1 and / or film 2 comprises at least one at least monoaxially oriented layer and the method comprises the steps:

a) Merging of film 1 and film 2, so that the region D comes into direct contact with layer B of the film 2; and

b) bonding of film 1 and film 2 by thermocompression at a pressure p and at a temperature T, where T is below T _m ^A and above T _V ^B.

Preferably, T is below T _V ^A and / or below T _m ^B.

In a preferred embodiment of the method according to the invention T is in the range of 50 ⁰ C to 130 ⁰ C, preferably 60 ° C to 130 ° C, more preferably 70 ⁰ C to 130 ° C, most preferably 80 ⁰ C to 130 ⁰ C and in particular 90 ⁰ C to 13O ⁰ C. In another preferred embodiment of the method according to the invention T is in the range of 50 ⁰ C to 130 ° C, more preferably 50 ° C to 120 ° C, more preferably 50 ⁰ C to 110 ° C, most preferably 50 ⁰ C to 100 ⁰ C and especially 50 ° C to 90 ° C.

Preferably, p is at least 5.0 N / mm, more preferably at least 10 N / mm, even more preferably at least 15 N / mm, most preferably at least 20 N / mm, and most preferably at least 25 N / mm. Preferably, the pressure p is in the range of 17.5 to 35 N / mm.

In a preferred embodiment of the method according to the invention, each section of the multilayer film is heated to the temperature T for a duration of at most 10 seconds, more preferably at most 5 seconds, even more preferably at most 1 second, most preferably at most 0.5 seconds and in particular at most 0.1 seconds ,

The invention further relates to a multilayer film, which is obtainable by the method described above.

Another object of the invention relates to a package comprising the multilayer film described above. Preferably, the package is a sealed tubular bag or a sealed package of trough and lid, the multi-layer film forming the lid.

The determination of the bond strength between layer A and layer B of the multilayer film according to the invention is preferably carried out in accordance with DIN 53 357 method B.

The determination of the curl of the multilayer film according to the invention is preferably carried out by the cross-cut method. The curl is defined as the distance of the rolled edges of a cross-cut, separated for the longitudinal and transverse directions. This distance is given in mm. The pattern is preferably taken from an inner layer of the roll of the multilayer film. For freshly made rolls, the pattern should be taken from a fixed position, ie at least the second layer of film. The sample should be removed from the roll immediately prior to measurement and the curl immediately measured.

In the preliminary test, it is determined to which side the film rolls, so that the pattern with the rolling tips is placed upwards. If the direction of roll is different in both test directions, it may be necessary to check 2 samples each with the outside and inside facing upwards. Patterns where the tip rolls against the surface can not be scored.

The measurement is preferably carried out at 23 ° C and medium humidity.

For this purpose, a template according to Figures 1 and 2 is placed so that the cuts are made diagonally to the direction of the film. The cutting length is 113 ± 1 mm in each case. Immediately after cutting, the template is removed. In Figures 1 and 2, the template comprises a sheet 1 of thickness 3 mm, two plastic ball heads 2 with a diameter of 32 mm, two countersunk screws 3, 2 nuts 4 and two washers 5. The distance between the two mutually parallel screw axes is 132 mm ,

30 seconds after cutting, the distance of the roll edges is measured separately for the longitudinal and the transverse direction, with low curl from tip to tip, with higher tendency to curl from inner edge to inner edge (see Figure 3).

The following examples serve to illustrate the invention, but are not to be interpreted as limiting.

Example 1 :

Multilayer films of the general structure ADB // C were produced by combining the composite AD and the composite BC. For this purpose, layer A was printed on one of its surfaces. The printed image was unchanged, ie without Treatment with a primer, combined with the composite B // C at the indicated temperatures under pressure.

The concrete structure of the individual layers is summarized in the following table; the bond adhesion (VH in [N / 15 mm]) between layers A and B measured in accordance with DIN 53 357 method B is indicated in the last column as a function of the temperature T:

As the above values for the composite adhesion show, depending on the composition of the polymers of layer A and layer B, a suitable temperature T can be found at which a bond strength of at least 1.0 N / 15 mm is achieved. The optimum temperature T can be found by simple routine experiments.

Example 2:

Analogously to Example 1, multilayer films of the general structure ADB // C were produced by combining the composite AD and the composite BC. For this purpose, however, was a Polytest laboratory laminating the Fa. Polytype used, wherein the speed 5 m / min and the temperature of the laminating roller 80 ⁰ C.

The concrete structure of the individual layers is summarized in the following table; the bond adhesion (VH) between layers A and B measured according to DIN 53 357 method B is indicated in the last column:

Comparative Example:

A commercially available, printed by extrusion lamination, printed and metallized (met) multilayer film was investigated with the following layer sequence:

Here, "P-E copolymer" means a layer based on a propylene-ethylene copolymer.

The layer thicknesses are summarized in the following table:

The bond adhesion values between the designated layers measured according to DIN 53 357 method B are summarized in the following table:

Claims

claims:

1. comprising multilayer film

Layer A, which is based on a thermoplastic polymer or a mixture of a plurality of thermoplastic polymers having a melting temperature T _m ^A and a VICAT softening temperature T _V ^A and has a layer thickness of at most 40 μm; and

Layer B, which is directly adjacent to layer A, is based on a thermoplastic polymer or a mixture of several thermoplastic polymers having a melting temperature T _m ^B and a VICAT softening temperature T _V ^B and a layer thickness of at most 50 μm; in which

T _V ^B <T _V ^A and T _m ^B <T _m ^A ; T _V ^B ≤ 115 ° C; the multilayer film comprises at least one at least monoaxially oriented layer; the multilayer film comprises an outer sealant layer; between layer A and layer B a printed and / or metallized and / or coated with a (half) metal oxide region D is arranged; and the bond strength between layer A and layer B is at least 1.0 N / 15 mm.

2. multilayer film according to claim 1, characterized in that it has a curl of at most 50 mm in the longitudinal and / or transverse direction.

3. multilayer film according to claim 1 or 2, characterized in that the bond strength between layer A and layer B at least 2.0 N / 15 mm, more preferably at least 3.0 N / 15 mm, more preferably at least 4.0 N / 15 mm is.

4. multilayer film according to any one of the preceding claims, characterized in that it comprises no laminating adhesive and / or no paint.

5. Multilayer film according to one of the preceding claims, characterized in that 70 ⁰ C <T _m ^A <260 ⁰ C.

6. multilayer film according to any one of the preceding claims, characterized in that they

- includes a total of not more than five layers and / or

- Has a total layer thickness of at most 200 microns.

7. Multilayer film according to one of the preceding claims, characterized in that independently of one another layer A and / or layer B

- is transparent and / or

- At least monoaxially stretched and / or

- forms a surface of the multilayer film.

8. Multilayer film according to one of the preceding claims, characterized in that independently of one another the total layer thickness

- Of layer B and all possibly on the side of layer B, which layer A is remote, arranged layers

in the range of 5.0 to 100 microns.

9. Multilayer film according to one of the preceding claims, characterized in that layer A is based on at least one polymer selected from the group consisting of (co) polyolefins, (co) polyesters and (co) polyamides.

10. multilayer film according to claim 9, characterized in that - The (co) polyolefin is selected from polyethylene (PE), polypropylene (PP) and their copolymers;

- The (co) polyester is selected from the group consisting of polyethylene terephthalate (PET), polybutylene terephthalate (PBT) and their copolymers; or

the (co) polyamide is selected from the group consisting of PA 4, PA 6, PA 7, PA 8, PA 9, PA 10, PA 11, PA 12, PA 4,2, PA 4,6, PA 6 , 6, PA 6,8, PA 6,9, PA 6,10, PA 6,12, PA 7,7, PA 8,8, PA 9,9, PA 10,9, PA 12,12, PA 6 / 6,6, PA 6,6 / 6, PA 6,2 / 6,2, and PA 6,6 / 6,9 / 6 and their copolymers.

11. Multilayer film according to one of the preceding claims, characterized in that layer B is metallized on the layer A side facing and / or

a layer thickness of at most 50% of the total layer thickness of the layer B and all on the side of layer B, which layer A is facing away, arranged layers and / or based on at least one (co) polyolefin.

12. Multilayer film according to claim 11, characterized in that layer B is based on polyethylene or an ethylene copolymer.

13. Multilayer film according to claim 12, characterized in that the ethylene copolymer is selected from the group consisting of ethylene-alkyl acrylate copolymer, ethylene-vinyl acetate copolymer, ethylene-maleic anhydride copolymer and ethylene-alkyl acrylate-maleic anhydride copolymer.

14. multilayer film according to any one of the preceding claims, characterized in that on the side of layer B, which layer A faces away, a layer C is arranged, which is based on a thermoplastic polymer and is stretched monoaxially or biaxially; and / or is transparent; and or

forms an outer surface of the multilayer film, and / or has a layer thickness in the range of 5.0 to 40 microns, and / or based on at least one (co) polyolefin.

15. Multilayer film according to claim 14, characterized in that layer C is based on polyethylene or an ethylene copolymer.

16. Multilayer film according to claim 14 or 15, characterized in that layer C is based on a (co) polyolefin or a mixture of several (co) polyolefins having a melting temperature T _m ^c and a VICAT softening temperature T _v ^c , wherein T _m ^c > T _m ^B and / or T _v ^c > T _V ^B.

17. Multilayer film according to one of claims 14 to 16, characterized in that layer B on a thermoplastic polymer or a mixture of several thermoplastic polymers having a density ρ ^B and a melt flow index MFI ^B and layer C on a (co) polyolefin or a mixture multiple (co) poly olefins having a density ρ ^c and a melt flow index MFI ^C , both p ^B and p ^{c being} in the range of 0.935 ± 0.015 g cm ^-3 and both MFI ^B and MFI ^C ranging from 2 , 5 ± 1, 0 g / 10 min (2.16 kg).

18. Multilayer film according to one of the preceding claims, characterized in that, in addition to layer A and layer B, it comprises the following layers in the following sequence:

- If necessary, a bonding agent layer HVi;

- If necessary, a polyamide PA ₁ ;

- A gas and / or aroma-dense barrier layer BA;

- If necessary, a polyamide PA2; and

- If necessary, a bonding agent HV ₂ .

19. A process for producing a multilayer film according to any one of claims 1 to 18 from

(I) a film 1 comprising layer A, which at least one of the two

Surface of the film 1 forms and on at least a part of this surface a printed and / or metallized and / or coated with a (half) metal oxide region D;

and

(ii) a film 2 comprising layer B, which forms at least one of the two surfaces of the film 2, this surface optionally being treated with a corona discharge; wherein film 1 and / or film 2 comprises at least one at least monoaxially oriented layer and the process comprises the steps of: a) combining film 1 and film 2 so that region D comes into direct contact with layer B of film 2; and b) bonding film 1 and film 2 by thermocompression at a pressure p and at a temperature T, where T is below T _m ^A and above T _V ^B.

20. The method according to claim 19, characterized in that T is below T _V ^A and / or below T _m ^B.

21. The method according to claim 19 or 20, characterized in that T is in the range of 50 ⁰ C to 130 ⁰ C.

22. The method according to any one of claims 18 to 21, characterized in that each portion of the multilayer film is heated to the temperature T at most for a period of 10 seconds.

23. Packaging comprising a multilayer film according to one of claims 1 to 18.

24. Packaging according to claim 23, characterized in that it is a sealed tubular bag or a sealed package of trough and lid, wherein the multi-layer film forms the lid.