Title of Invention

MULTILAYER FILM

Abstract An adhesion promoter which comprises from 2 to 100% by weight of a copolymer which contains the following monomer units: a) from 70 to 99.9% by weight of monomer units which derive from vinyl compounds selected from acrylic acid derivatives, methacrylic acid derivatives, and vinylaromatics, and also b) from 0.1 to 30% by weight of monomer units which contain a functional group selected from a carboxylic anhydride group, an epoxy group, and an oxazoline group, is used for production of a bond between I. a layer composed of a polyamide molding compound, and II. a part composed of an ABS molding composition.
Full Text

Multilayer film
The present invention relates to a multilayer film which comprises at least one layer composed of a polyamide (PA), and also comprises a specific adhesion promoter, and which is suitable for bonding to ABS as substrate material.
The current standard process for decoration of external areas on automobiles is painting. However, this procedure firstly generates high manufacturing costs, resulting from provision of specific plant and the operating cost associated therewith for the automobile producer, and secondly causes pollution of the environment. Pollution of the environment derives by way of example from solvent constituents released from the paints used, and also from accumulation of paint residues, which have to follow correct disposal routes.
Another factor is that painting has only limited suitability for decorating the surfaces of plastics components, which in recent years have become more popular in automobile construction, because of the saving in weight and cost
The process of painting plastics components which are components of bodywork can, for example, be carried out on-line, the plastics part being subjected to a paint treatment identical with that for the metallic components. This leads to a uniform color, but is attended by high temperatures resulting from the cathodic electrodeposition method conventional here, and this makes the selection of material more difficult. In addiiiorL identical adhesion of the paint formulation has to be ensured on very different substrates. If the process of painting the plastics parts is carried out in a separate step (known as off-line painting), comprising process conditions more advantageous for plastics, the problem of colormatching arises, meaning that the shade achieved on the metal has to be matched precisely. However, the differences in substrate and in the underlying paint formulation that can be used, and process conditions, make this very difficult to achieve. If there is a color difference prescribed via the design, a serious disadvantage that remains is provision of a second set of painting equipment for the plastics parts and the cost associated therewith, and additional time required for manufacture of the automobile also has to be considered. Direct use of the untreated, generally injection-

molded plastics parts is aesthetically disadvantageous, because surface defects resulting from the process, such as weld lines, air inclusions, and also necessary reinforcing fillers, such as glass fibers, are clearly discernible here. This is intolerable in visible regions. Consequently, improvement of surface quality has to be undertaken, for example in the context of a painting process, frequently requiring much work for pretreatment via polishing and application of relatively thick layers of a primer.
One proposed solution consists in the use of multilayered plastics films, used to cover the components and then requiring no painting. The bond between substrate and decorating film here can be achieved via a number of manufacturing processes. By way of example, the film can be laminated to the substrate, or it is possible to select a process of reverse coating by an injection-molding process, in which the film is placed in the injection mold during component production. The concept of a film as carrier of decoration is also in line with a trend toward individualization of design elements on automobiles. Specifically, this trend leads to a wider range of models in the manufacturing process, but with a reduction in the number of respective components manufactured per series. The use of films permits rapid, problem-free design change, and can therefore meet this challenge. An important factor here is that the film complies with the standards demanded in the automobile industry with respect to surface properties (class A surface), solvent resistance, and appearance.
Decorative films of this type are in principle known. EP 0 949 120 Al describes by way of example decorative films with polyalkyl methacrylate as base layer, and these can also comprise a polyamide support layer on the substrate side, while WO 94/03337 discloses decorative films whose base layer can be composed of a wide variety of polymer alternatives, among which is polyamide.
Polyamides, in particular polyamides based on PA12 or PA612. have a property profile, for example impact resistance and chemicals resistance, giving them good suitability for production of decorative films of this type. Paint systems have an underlying tendency toward brittle fracture. If a plastics component decorated in this way is exposed to impact, the crack propagates from the paint layer into the substrate situated thereunder, the result being damage extending far into the material. In contrast, the use in particular of materials with low-

Temperature impact resistance in a decorative film covering the substrate avoids damage to outer skin and substrate. A fact which has to be considered here is that sufficient chemicals resistance, in particular with respect to engine fuels, oils, and fats must be achieved simultaneously. These requirements are met by polyamides such as PA 12, PA 11 or PA 612. Polyamides which contain aliphatic structures moreover have advantageous UV aging performance. This means that the tendency toward yellowing is only very slight and cannot lead to undesired color changes during the course of the lifetime of an automobile. This combination of properties cannot be generated in the same way by other plastics. Another factor which has to be considered, alongside advantageous properties of the decorated molding, is the suitability of a film of this type with respect to economically advantageous processing methods. A particular factor to be emphasized here in the case of polyamides is good thermoforming performance. The reason for this is that the polyamide materials have inherently high tensile strain at break, which gives them an advantage over other materials.
An object, in the overall context of the application, is to find a suitable adhesion promoter which permits coupling of the polyamide layer to the substrate. A frequently utilized substrate material is ABS or its blend with polycarbonate (PC), which in some cases has reinforcement via glass fibers or via other fillers. The adhesion promoter has to be suitable for processing in a coextrusion process to give a layer within a multilayer film. Hie composite of this multilayer film with the substrate material can then by way of example be produced via reverse coating by an injection-molding method, or via lamination. A factor applicable not only during the coextrusion process to give the multilayer film but also during reverse coating by an injection-molding method or during lamination is that increased requirements are placed here upon the bonding power of the adhesion promoter, because there is no forced mixing of the components permitting complete consumption of reactive groups at the phase boundary by way of continuous surface renewal. Furthermore, for example during reverse coating by an injection-molding method, the time for which the temperature in the contact zone of the idherends is sufficiently high to achieve formation of a composite is only short. The two ibovementioned specifications provide no help toward achievement of this object.
JS 3 561 493 discloses that two layers composed of various polymers can be bonded via an ntermediate layer which is composed of a mixture of these polymers, by means of

Co extrusion. However, this teaching is not transferable to the polyamide/ABS system. The outcome of US 3 561 493 applies only to a multilayer tube system in which a polyethylene layer is made to adhere to a PA 11 via use of a blend composed of the two materials. It was impossible to transfer this teaching to bonding between polyamide or a polyether block amide derived therefrom and ABS, because no composition could be found that provided adequate, reliable adhesion to the two materials.
Furthermore, EP 0 322 558 A2 describes blends composed of amorphous polyamide and ABS. EP 0 601 752 Al describes the use of these blends as adhesion promoters for the amorphous PA/ABS system. These compounded adhesion-promoter materials can be used in coextruded multilayer films. However, experiments have shown that this concept cannot be successfully applied for semi crystalline polyamides, e.g. PA 12 or polyether block amide (PEBA) derived from PA12, because blends of this type of composition do not achieve reliable adhesion to the two materials in the desired composite system.
An object was therefore to develop a coextruded adhesion promoter for coupling of polyamides in general and in particular of polyamides based on PA12 to ABS.
This object, and other objects apparent hereinafter, are achieved via the use of an adhesion promoter for production of a bond between
I. a layer composed of a polyamide molding compound and
II. a part composed of an ABS molding composition,
where the adhesion promoter comprises from 2 to 100% by weight of a copolymer which contains the following monomer units:
1. from about 70 to about 99.9% by weight of monomer units which derive from vinyl
compounds selected from acrylic acid derivatives, methacryiic acid derivatives, and
vinylaromatics, and also
2. from about 0.1 to about 30% by weight of monomer units which contain a functional
group selected from a carboxylic anhydride group, an epoxy group, and an oxazoline
group.

There is no restriction on the polyamide of the layer I. Polyamides that can be used are mainly aliphatic homo- and copolycondensates, such as PA 46, PA 66, PA 88, PA 610, PA 612, PA 810, PA 1010, PA 1012, PA 1212, PA 6, PA 7, PA 8, PA 9, PA 10, PA 11 and PA 12. (The terminology for the polyamides corresponds to an international standard where the first numeral(s) give(s) the carbon number of the starting diamine and the second numeral(s) give(s) the carbon number of the dicarboxylic acid. If only one numeral is given, this means that the starting material was an V,T-aminocarboxylic acid or the lactam derived therefrom; for further information reference may be made to H. Domininghaus. Die Kunststoffe and ihre Eigenschaften [Plastics and their properties], pp. 272 ff., VDI-Verlag, 1976.)
If copolyamides are used these may contain, by way of example, adipic acid, sebacic acid, suberic acid, isophthalic acid, terephthalic acid, naphthalene-2.6-dicarboxylic acid, etc. as coacid and, respectively, bis(4-aminocyclohexyl)methane, trimethvlhexamethylenediamine, hexamethylenediamine or the like as codiamine. There may also be lactams, such as caprolactam or laurolactam, or aminocarboxylic acids, such as T-axninoundecanoic acid, incorporated as cocomponent.
The preparation of these polyamides is known (e.g. D. B. Jacobs. J. Zimmermann, Polymerization Processes, pp. 424 - 467, Interscience Publishers, New York, 1977; DE-B 21 52 194).
Other suitable polyamides are mixed aliphatic/aromatic polyeomknsaies. e.g. as described in US patents 2 071 250, 2 071 251, 2 130 523, 2 130 948, 2 241 322, 2 312 966, 2 512 606, and 3 393 210, and in Kirk-Othmer, Encyclopedia of Chemical Technology, 3rd edn., vol. 18, pp. 328 ff. and 435 ff, Wiley & Sons, 1982. Other suitable polyamides are poly(etheresteramides) or poly(etheramides); products of this type are described by way of example in DE-A 25 23 991, DE-A 27 12 987 and DE-A 30 06 961.
The polyamide molding composition can either comprise one of these polyamides or two or more in the form of a mixture. As long as other thermoplastics do not impair bonding capability, up to 40% by weight of these can moreover be present, in particular impact-

modifying rubbers, such as ethylene-propylene copolymers or ethylene-propylene-diene copolymers (EP-A-0 295 076), polypentenylene, polyoctenylene, random or block copolymers composed of alkenyl aromatic compounds with aliphatic olefins or dienes (EP-A-0 261 748), or core-shell rubbers with a tough, resilient core composed of (meth)acrylate rubber, of butadiene rubber, or of styrene-butadiene rubber with glass transition temperatures Tg The polyamide molding composition can receive additions of the auxiliaries and additives conventional for polyamides, examples being flame retardants, stabilizers, plasticizers, processing aids, fillers, in particular for improving electrical conductivity, reinforcing fibers, pigments, or the like. The amount added of the agents mentioned is to be such as not to give any serious impairment of the desired properties.
In one preferred embodiment, the monomer units of the polyamide which derive from diamine and dicarboxylic acid and, respectively, lactam (or aminocarboxyiic acid) have an average of at least 8 carbon atoms and particularly preferably at least 9 carbon atoms.
The layer composed of the polyamide molding composition can be produced by any of the familiar industrial methods, particularly advantageously via extrusion or coextrusion.
ABS polymers have long been prior art and many commercial grades of these are available. They are in essence composed of acrylonitrile, butadiene, and styrene; this three-monomer system can be varied widely in order to meet the respective requirements. The polymer contains chains composed of polybutadiene, polyisoprene. acrylonitrile-butadiene rubber (NBR), styrene-butadiene rubber (SBR), or the like, onto which styrene, or preferably a styrene-acrylonitrile mixture has been grafted; the mixture can moreover also comprise other comonomers, e.g. methyl methacrylate.
In typical cases here, the rubber content is from 5 to 30% by weight; the matrix composed of styrene-acrylonitrile copolymer usually contains from 10 to 45% by weight and in particular

From 15 to 35% by weight of aciylonitrile. As a result of the preparation process, at least some of this copolymer has been grafted onto the rubber, while the remainder is present in ungrafted form.
The ABS molding composition can comprise the usual additives, e.g. plasticizers, processing aids, flame retardants, stabilizers, antistatic agents, fillers, pigments, and reinforcing agents. Besides these, other thermoplastics can be present as constituents in the ABS molding composition, examples being polycarbonates, polyamides, or polyesters.
For the purposes of the invention, a part composed of this ABS molding composition is bonded to the layer composed of a polyamide molding composition. This part may have been shaped in the form of a sheet, for example a bodywork part of an automobile, e.g. roof module, wheel surround, engine cover, or door. Other advantageous embodiments alongside these are those in which elongate components with some degree of curvature are produced, for example cladding, e.g. the cladding of what are known as A columns on an automobile or decorative and cover strips of any type. Another example is provided by protective cladding for door sills. Alongside applications on the exterior of an automobile, constituents of the interior can also be advantageously decorated via the inventive films, in particular decorative elements such as strips and panels, because impact resistance and resistance to chemicals, such as cleaning compositions, is also a requirement in the interior. The structures listed are naturally suitable not only for use as in an automobile but also for decorative elements of any type in exterior or interior applications. In all of these cases. the part composed of the ABS molding composition forms the substrate which is bonded to the multilayer film, or it can form one layer of this film, in turn intended to be bonded to a substrate composed of an ABS molding composition.
The adhesion promoter comprises, as active agent, from 2 to 100% by weight, preferably from 3 to 80% by weight, particularly preferably from 4 to 60% by weight, and with particular preference from 5 to 40% by weight, of a copolymer, which preferably contains the following monomer units:
1. from about 70 to about 99.9% by weight, preferably from 80 to 99.4% by weight, and particularly preferably from 85 to 99% by weight, of monomer units selected from units

of the following formulae:

where R1 = H or CH3 and R2 = H, methyl, ethyl, propyl or butyl;

where R is as above and R and R , independently of one another, are identically H methyl or ethyl;

where R1 is as above;

where R5 = H or CH3;

where R1 is as above and R6 = H, methyl, ethyl, propyl, butyl or phenyl, and m = 0 or 1;
2. from about 0.1 to about 30% by weight, preferably from 0.6 to 20% by weight, and particularly preferably from 1 to 15% by weight, of monomer units selected from units of the following formulae:

where R1 is as above;
(VIII)
Where R1 is as above.
The reason for limiting the chain length in substituents R1 to R is that longer alkyl radicals lead to a lower glass transition temperature and thus to lower heat resistance. This may be acceptable in a particular case; embodiments of this type are at least within the scope of equivalence of the invention.
The units of the formula (I) derive by way of example from acrylic acid, methacrylic acid, methyl acrylate, ethyl acrylate, n-butyl acrylate, methyl methaeryiate, n-propyl methacrylate, or isobutyl methacrylate.
The units of the formula (II) derive by way of example from acryiamide. methacrylamide, N-methylacrylamide, N-methylmethacrylamide, or N,N-dimethylaciylainIde.
The units of the formula (III) derive from acrylonitrile or methacryionitrile.
The units of the formula (IV) derive from styrene or a-methylstyrene; these can be replaced entirely or to some extent by other polymerizable aromatics, such as p-methylstyrene or indene, which have the same effect.
If m = 0, the units of the formula (V) derive from unsubstituted or substituted maleimides, such as maleimide, N-methylmaleimide, N-ethylmaleimide, N-phenylmaleimide, or N-methylaconitimide. If m = 1, they derive via reaction with ammonia or with a primary amine

Of two adjacent units of the formula (I) in a polymer, forming an imide.
If m = 0, the units of the formula (VI) derive from unsubstituted or substituted maleic anhydrides, such as maleic anhydride or aconitic anhydride. These latter compounds can be replaced entirely or to some extent by other unsaturated anhydrides, e.g. itaconic anhydride, which have the same effect. If m = 1, they derive via elimination of water from two adjacent units of the formula (I) in a polymer (R = H), with ring closure.
The units of the formula (VII) derive from glycidyl acrylate or glycidyl methacrylate, and the units of the formula (VIII) derive from vinyloxazoline or isopropenyloxazoline.
Various embodiments of the copolymer are preferred, and contain the following units:
A. from 14 to 96% by weight, preferably from 20 to 85% by weight and particularly preferably from 25 to 75% by weight, of units of the formula (I), where R2 is not H;
From 0 to 75% by weight, preferably from 1 to 60% by weight, and particularly preferably from 5 to 40% by weight, of units of the formula (V)? where m = 1;
from 0 to 15% by weight, preferably from 0 to 10% by weight, and particularly preferably from 0.1 to 7% by weight, of units of the formula (I), where R~ = H:
from 0.1 to 30% by weight, preferably from 1 to 20% by weight and particularly preferably from 2 to 15% by weight, of units of the formula (VI). where m = 1.
If units of the formula (V) are present, these copolymers are termed polyacrylimides or polymethacrylimides or sometimes also polyglutarimides. These are products which come from polyalkyl acrylates and, respectively, polyalkyl methacrylates, in which two adjacent carboxylate groups have been reacted to give a cyclic imide. The imide is preferably formed with ammonia or with primary amines, e.g. methylamine, in the presence of water, and the units of the formula (VI) and, where appropriate, units of the formula (I), where R2 = H, are produced concomitantly via hydrolysis. The products are known, as

Also is their preparation (Hans R. Kricheldorf, Handbook of Polymer Synthesis, Part A, Verlag Marcel Dekker Inc. New York-Basel-Hongkong, pp. 223 et seq., H. G. Elias, Makromolekiile [Macromolecules], Hiithig und Wepf Verlag Basel-Heidelberg-New York; US 2 146 209 A; US 4 246 374). If water only is used for the reaction, the product is units of the formula (VI) and also, if appropriate, acidic units (I) via hydrolysis, without formation of imide units (VI).
B. from 40 to 99.9% by weight, preferably from 45 to 99.4% by weight, and particularly
preferably from 50 to 99% by weight, of units of the formula (IV);
From 0 to 45% by weight, preferably from 0.1 to 40% by weight, and particularly preferably from 2 to 35% by weight, of units of the formula (III);
From 0.1 to 30% by weight, preferably from 0.6 to 20% by weight, and particularly preferably from 1 to 15% by weight, of units of the formula (VI), where m = 0.
Copolymers of this type are obtainable in a known manner via free-radical-initiated copolymerization of aliphatically unsaturated aromatics, of unsaturated carboxylic anhydrides, and, if appropriate, of acrylonitrile or methacrjlonitrile-
C. from 0.1 to 99.9% by weight, preferably from 2 to 99.4% by weight and particularly
preferably from 5 to 99% by weight, of units of the formula (I);
From 0 to 99.7% by weight, preferably from 2 to 99.3% by weight, and particularly preferably from 4 to 98% by weight, of units of the formula (IV);
from 0.1 to 30% by weight, preferably from 0.6 to 20% by weight, and particularly preferably from 1 to 15% by weight, of units of the formula (VI), where m = 0. Copolymers of this type are obtainable in a known manner via free-radical-initiated copolymerization of acrylic acid, methacrylic acid, and/or esters thereof, and, if appropriate, of aliphatically unsaturated aromatics, and also of unsaturated carboxylic anhydrides.

D. from 0.1 to 99.7% by weight, preferably from 2 to 99.3% by weight, and particularly
preferably from 5 to 98% by weight, of units of the formula (I);
From 0.1 to 45% by weight, preferably from 1 to 40% by weight, and particularly preferably from 2 to 35% by weight, of units of the formula (III);
From 0.1 to 30% by weight, preferably from 0.6 to 20% by weight, and particularly preferably from 1 to 15% by weight, of units of the formula (VT), where m = 0.
Copolymers of this type are obtainable in a known manner via free-radical-initiated copolymerization of acrylic acid, methacrylic acid, and/or esters thereof acrylonitrile or methacrylonitrile, and of unsaturated carboxylic anhydrides.
E. ABS polymer which contains from 0.1 to 30% by weight, preferably from 0.6 to 20% by
weight, and particularly preferably from 1 to 15% by weight of units of the formula (VT),
where m = 0, These can have been polymerized into the chains or can have been grafted
onto the chains.
F. from 0 to 99.9% by weight, preferably from 0.1 to 99.4% by weight, and particularly
preferably from 2 to 99% by weight, of units selected from the formulae (I)? where R2 is
not H, and (III),
From 0 to 99.7% by weight, preferably from 0.1 to 99.4% by weight, and particularly preferably from 2 to 99% by weight, of units of the formula (IV),
from 0.1 to 30% by weight, preferably from 0.6 to 20% by weight, and particularly preferably from 1 to 15% by weight, of units of the formula (VII).
G. from 0 to 99.9% by weight, preferably from 0.1 to 99.4% by weight, and particularly
preferably from 2 to 99% by weight, of units selected from the formulae (I), where R is
not H, and (III),

From 0 to 99.7% by weight, preferably from 0.1 to 99.4% by weight, and particularly preferably from 2 to 99% by weight, of units of the formula (IV),
From 0.1 to 30% by weight, preferably from 0.6 to 20% by weight, and particularly preferably from 1 to 15% by weight, of units of the formula (VIII),
The copolymer can always contain other additional monomer units, such as those which derive from maleic diesters, from fumaric diesters, from itaconic esters, from vinyl acetate, or from ethene, as long as the desired adhesion-promoting effect is not substantially impaired thereby.
In one embodiment, the adhesion promoter can be composed entirely of the copolymer, in a variant of this, the copolymer comprises an impact modifier, e.g. an acrylate rubber.
In a second embodiment, the adhesion promoter comprises from 2 to 99,9% by weight, preferably from 3 to 80% by weight, particularly preferably from 4 to 60% by weight, and with particular preference from 5 to 40% by weight, of the copolymer, and also from 0.1 to 98% by weight, preferably from 20 to 97% by weight, particularly preferably from 40 to 96% by weight, and with particular preference from 60 to 95% by weigh!, of ABS.
In a third embodiment, the adhesion promoter comprises from 2 to 99.9% by weight, preferably from 3 to 80% by weight, particularly preferably from 4 to 6O°-o by weight, and with particular preference from 5 to 40% by weight, of the copoiymer. and also from 0.1 to 98% by weight, preferably from 20 to 97% by weight, particularly preferably from 40 to 96% by weight, and with particular preference from 60 to 95% by weight, of polyamide. An impact modifier, e.g. an EPM rubber, is also present, if appropriate.
In a fourth embodiment, the adhesion promoter comprises from 2 to 99.8% by weight, preferably from 3 to 80% by weight, particularly preferably from 4 to 60% by weight, and with particular preference from 5 to 40% by weight, of the copolymer, and also
From 0.1 to 97.9% by weight, preferably from 5 to 92% by weight, particularly preferably

From 10 to 86% by weight, and with particular preference from 20 to 75% by weight, of ABS, and also
from 0.1 to 97.9% by weight, preferably from 5 to 92% by weight, particularly preferably from 10 to 86% by weight, and with particular preference from 20 to 75% by weight, of polyamide.
The adhesion promoter can comprise the usual auxiliaries and additives, e.g. flame retardants, stabilizers, plasticizers, processing aids, pigments, or the like. The amount of the agents mentioned added is to be such as not seriously to impair the desired properties.
The invention further provides multilayer films which comprise at least one layer composed of a polyamide molding composition, and also comprise at least one layer composed of the inventive adhesion promoter, and also composite parts composed of tins multilayer film, and also of a part composed of an ABS molding composition.
As a function of the application, the film can comprise, alongside the layers present according to the invention and composed of a polyamide molding composition and the adhesion promoter as claimed, other layers, such as a support layer composed of an ABS molding composition on the substrate side, a color layer, a functional layer, a further polyamide layer, and/or an outer layer or a clearcoat.
The color layer can be a lacquer layer; however, it is preferably composed as in the prior art, of a colored thermoplastics layer. The thermoplastic can be a polyamide or a polymer compatible with polyamide. The colorants used can comprise organic dyes or inorganic or organic pigments.
The functional layer is a layer which has an advantageous effect on the properties of the film in relation to performance requirements, irrespective of the color, for example with regard to mechanical properties or resistance, for example to UV or heat. It can be composed of any desired molding composition which meets the performance demands and has the required adhesion to the adjacent layers, for example of polyamide, polyester, or polycarbonate.

The clearcoat can by way of example be composed, as in the prior art, of polyamide, of an acrylate polymer, of a fluoropolymer, or of a mixture thereof It is intended to ensure that the required visual surface properties are present, and to protect the layers situated thereunder.
Examples of useful layer configurations for the inventive film are:
PA / Adhesion promoter (AP)
PA / AP / ABS
Functional layer / PA / AP
Functional layer / PA / AP / ABS
PA / Functional layer / PA / AP
PA / Functional layer / PA / AP / ABS
Clearcoat / PA / Functional layer / PA / AP
Clearcoat / PA / Functional layer / PA / AP / ABS
Clearcoat / Functional layer / PA / AP
Clearcoat / Functional layer / PA / AP / ABS
Clearcoat / Color layer / PA / AP
Clearcoat / Color layer / PA / AP / ABS
Clearcoat / PA / AP
Clearcoat / PA / AP / ABS
Clearcoat / Colored PA / AP
Clearcoat / Colored PA / AP / ABS
By way of example, coextrusion or lamination can be used to produce the multilayer film, and, if appropriate, as in the prior art, this is followed by a process such as forming, lacquering, or surface finishing (for example by means of plasma treatment).
A peelable protective film can also be laminated onto the finished multilayer film and provides protection during transport or installation, and is peeled away after production of the composite part.
Careful balance of individual properties makes the inventive film particularly suitable for meeting the requirements placed upon materials for decorative films in the automobile

Exterior and automobile interior sectors. The adhesion promoter claimed ensures the presence of a reliably adhering bond between the polyamide layer and ABS, which is a frequently encountered substrate material. This applies not only in cases where ABS is brought into contact with the adhesion promoter via reverse coating by an injection-molding method, but also in cases where ABS is extruded onto the adhesion promoter, for example in a coextrusion process, or where the composite is produced via compression molding, lamination, or reverse coating by a compression-molding or foaming method. Adhesion is also ensured when, prior to reverse coating by an injection-molding process, the film is subjected to a forming process, such as thermoforming, or when the composite part is formed after production.
The examples below are intended to illustrate the invention. The following materials were used in the examples:
1. Clearcoat:
PA I: A PA 12 whose relative solution viscosity r|rei, measured in a 0.5% strength by weight solution in m-cresol at 23°C to ISO 307, is 2.1
PA II: RILSAN® BESN TL, a PA 11 from Arkema whose relative solution viscosity r|rei is 2.1
2. Polyamide molding composition:
PA III: mixture composed of 20 parts by weight of a PA 12 whose relative solution viscosity rjrei is 2.1 and which has an excess of amino end groups, 80 parts by weight of a polyetheresteramide based on PA 12 and polytetrahydrofiiran, and also 0.5 part by weight of carbon black pigment
PA IV: mixture composed of 20 parts by weight of a PA 12 whose relative solution viscosity rrel is 1.9 and which has an excess of carboxy end groups, 80 parts by weight of a polyetheresteramide based on PA 12 and polytetrahydrofuran, and also

2 parts by weight of aluminum flakes
PA V: mixture composed of 100 parts by weight of PA II and 2 parts by weight of aluminum flakes
3. Adhesion promoter:
AP I: mixture composed of 60 parts by weight of TERLURAN(S) GP22, an ABS from BASF AG, and 40 parts by weight of a copolymer whose composition is
a) 57% by weight of monomer units of the formula

c) 3% by weight of monomer units of the formula


The copolymer, a polymethacrylimide, can be prepared via reaction of a melt of polymethyl methacrylate (PMMA) with an aqueous methyiannne solution, for example in an extruder,
AP II: mixture composed of 55 parts by weight of a PA 12 whose relative solution viscosity rjrei is 1.9 and which has an excess of carboxy end groups, and 45 parts by weight of a copolymer identical with that in AP I
AP III: mixture composed of 40 parts by weight of TERLURANrt GP22^ 30 parts by weight of a PA 12 identical with that in AP II, and 30 parts by weight of a copolymer identical with that in AP I
AP IV: mixture composed of 50 parts by weight of TERLURAN* GP22.25 parts by weight of a PA 12 identical with that in AP II, and 25 parts by weight of a copolymer identical with that in AP I
AP V: (non-inventive): mixture composed of 40 parts by weight of TERLURAN® GP22 and 60 parts by weight of a PA 12 identical with that in AP II

AP VI: (non-inventive): mixture composed of 60 parts by weight of TERLURAN® GP22 and 40 parts by weight of a PA 12 identical with that in AP II
AP VII: (non-inventive): mixture composed of 50 parts by weight of TERLURAN® GP22 and 50 parts by weight of a PA 12 identical with that in AP II
AP VIII: mixture composed of 40 parts by weight of TERLURAN® GP22, 30 parts by weight of PA II, and 30 parts by weight of a copolymer identical with that in AP I
4. Material used for reverse coating by an injection-molding method:
TERLURAN® GP22G4nf, an ABS from BASF AG with 20% by weight of glass fiber
The molding compositions were prepared using an Automatik ZCM4146-21D kneader, melt temperature being 250°C, melt throughput being 12kg/h, and rotation rate being 250 rpm.
The multilayer films were produced on a plant from Collin, using a take-off speed of 2.5 m/min. The individual extruded layers were combined and run through a calender. The width of the films was 24 cm.
Reverse coating by an injection-molding method took place on an Engel ES600/150 machine using a mold temperature of 80°C and a melt temperature of 280°C. The film was cut to 100 mm x 150 mm format here and placed in a mold (sheet 105 mm x 150 mm x 0.8 - 10 mm). The thickness of the sheet inclusive of film was 3 mm after reverse coating by an injection-molding method.
In order to determine resistance to separation, this being a measure for the quality of adhesion of the bond between adhesion-promoter layer and substrate, a test specimen of dimensions 10 mm x 130 mm was stamped out from the sheet and subjected to a peel test. To determine quality of adhesion within the multilayer film, a test specimen with the same dimensions was stamped out from the multilayer film and a similar procedure was used. If there is good

Adhesion between the bond partners studied, one end of the test specimen was kept in hot polyethylene glycol for 30 minutes in order to initiate separation. Once separation had been initiated, the test specimen was clamped into the chucks of the test machine with an angle of 180° between the layers to be separated. The chucks then separated at a velocity of 50mm/min, thus subjecting the test specimen to severe peel conditions. The separation resistance exerted by the composite in the face of these peel conditions was recorded. This was achieved by measuring the separation force needed for separation in N. Separation resistance was determined from this by suppressing separation force measured in relation to the specimen width, by taking the quotient. Specimen width was always 10 mm, and separation resistance therefore has the unit N/mm. It is regarded as sufficient if it is at least 3 N/mm.



What is claimed is:
1. The use of an adhesion promoter which comprises from 2 to 100% by weight of a copolymer which contains the following monomer units:
a) from 70 to 99.9% by weight of monomer units which derive from vinyl compounds selected from acrylic acid derivatives, methacrylic acid derivatives, and vinylaromatics, and also
b) from 0.1 to 30% by weight of monomer units which contain a functional group selected from a carboxylic anhydride group, an epoxy group, and an oxazoline group,
for production of a bond between
I. a layer composed of a polyamide molding compound, and
II. a part composed of an ABS molding composition.
2. The use as claimed in claim 1, characterized in that
the copolymer contains the following monomer units:
a) from 70 to 99.9% by weight of monomer units selected from units of the following formulae:
(i)
where R = H'or CH3 and R = H, methyl, ethyl, propyl or butyl;


where R1 is as above and R3 and R4, independently of one another, are identically H, methyl or ethyl;

where R1 is as above;

where R5 = H or CH3;

where R1 is as above and R6 = H, methyl, ethyl, propyl, butyl or phenyi, and m = 0 or
b) from 0.1 to 30% by weight of monomer units selected from units of the following formulae:

where R1 and m are as above;

where R1 is as above;

where R1 is as above.
3. The use as claimed in claim 1 or 2, characterized in that the adhesion promoter comprises
From 2 to 99.9% by weight of the copolymer, and from 0.1 to 98% by weight of ABS.
4. The use as claimed in claim 1 or 2, characterized in that
the adhesion promoter comprises
From 2 to 99.9% by weight of the copolymer, and from 0.1 to 98% by weight of polyamide.
5. The use as claimed in claim 1 or 2, characterized in that
the adhesion promoter comprises
From 2 to 99.8% by weight of the copolymer, from 0.1 to 97.9% by weight of ABS, and from 0.1 to 97.9% by weight of polyamide.
6. A multilayer film which comprises the following layers:
- at least one layer composed of a polyamide molding composition, and also
- at least one layer composed of the adhesion promoter as claimed in any of claims 1 to
5.
7. The multilayer film as claimed in claim 6, characterized in that
it comprises one or more other layers selected from an ABS layer, another polyamide layer, a color layer, a functional layer, and a clearcoat.
8. A process for production of a multilayer film as claimed in claim 6 or 7, characterized in that
the multilayer film is produced via coextrusion or lamination, and also via a process

Which follows, if appropriate.
9. A composite part composed of
- a multilayer film as claimed in claim 6 or 7, and
- a part composed of an ABS molding composition.
10. The composite part as claimed in claim 9, characterized in that
the ABS molding composition comprises other thermoplastics as constituents.
11. The composite part as claimed in claim 9 or 10, characterized in that
the part composed of an ABS molding composition has been shaped in the form of a sheet.
12. The composite part as claimed in any of claims 9 to 11, characterized in that
it is a bodywork part of an automobile, is a cladding, is a decorative strip, is a cover strip, is a panel, or is a decorative element.
13. A process for production of a composite part as claimed in any of claims 9 to 12, characterized in that
the composite part is produced via coextrusion, pressing, lamination, or via reverse coating by an injection-molding, compression-molding, or foaming method, and also, if appropriate, via subsequent forming.


Documents:

4598-CHENP-2006 OTHER PATENT DOCUMENT 08-10-2010.pdf

4598-chenp-2006 other patent document 8-10-2010.pdf

4598-CHENP-2006 AMENDED PAGES OF SPECIFICATION 08-10-2010.pdf

4598-CHENP-2006 AMENDED CLAIMS 08-10-2010.pdf

4598-CHENP-2006 EXAMINATION REPORT REPLY RECIEVED 08-10-2010.pdf

4598-chenp-2006 form-1 08-10-2010.pdf

4598-chenp-2006 form-3 08-10-2010.pdf

4598-CHENP-2006 CORRESPONDENCE-OTHERS 01-02-2010.pdf

4598-CHENP-2006 FORM-13 15-02-2010.pdf

4598-chenp-2006-abstract.pdf

4598-chenp-2006-claims.pdf

4598-chenp-2006-correspondnece-others.pdf

4598-chenp-2006-description(complete).pdf

4598-chenp-2006-form 1.pdf

4598-chenp-2006-form 26.pdf

4598-chenp-2006-form 3.pdf

4598-chenp-2006-form 5.pdf

4598-chenp-2006-pct.pdf


Patent Number 244945
Indian Patent Application Number 4598/CHENP/2006
PG Journal Number 53/2010
Publication Date 31-Dec-2010
Grant Date 27-Dec-2010
Date of Filing 15-Dec-2006
Name of Patentee EVONIK DEGUSSA GMBH
Applicant Address RELLINGHAUSER STRASSE 1-11, 45128 ESSEN
Inventors:
# Inventor's Name Inventor's Address
1 WURSCHE ROLAND SPIEKERHOF 20 48249 DULMEN GERMANY
2 BOLLMANN SONJA PLAGGENHEIDE 2 45721 HALTERN AM SEE GERMANY
3 ALTING KIRSTEN GASSELSTIEGE 40 48159 MUNSTER GERMANY
4 WIELPUTZ MARTIN LOHAUSWEG 19 48145 MUNSTER GERMANY
5 HAGER HARALD BRENTANOSTRASSE 2 63579 FREIGERICHT GERMANY
PCT International Classification Number B32B 27/34
PCT International Application Number PCT/FR05/52675
PCT International Filing date 2005-06-09
PCT Conventions:
# PCT Application Number Date of Convention Priority Country
1 10 2004 025 217.5 2004-06-16 Germany