DE202017003329U1 - Adhesive tape and foil - Google Patents

Abstract

Adhesive tape with a carrier made of a film, to which an adhesive is applied at least on one side, the film being a monoaxially stretched film containing at least 95% by weight, preferably 99% by weight, more preferably 100% by weight. % of propylene polymer composition having different phases, comprising the following components:
i) 80 to 99% by weight, preferably 93 to 96% by weight, based on the total weight of components i) and ii) of a propylene polymer matrix comprising a propylene homopolymer and more preferably a preferably random propylene copolymer having a comonomer compound selected from ethylene or C ₄ to C ₁₀ α-olefins, the propylene polymer matrix having a comonomer content of not more than 15% by weight;
ii) 1 to 20 wt .-%, preferably 4 to 7 wt .-%, based on the total weight of components i) and ii), of an elastomer in the form of an ethylene-propylene copolymer having an ethylene content of 50 to 90 wt. -%.

Description

The invention relates to an adhesive tape and a film.

So-called strapping tapes are particularly suitable for bundling objects. Such items are for example tubes, profiles or stacked boxes (strapping application).

Furthermore, the strapping applications include the fixation of moving parts on white devices (such as refrigerators and freezers or air conditioning units), on red devices such as (gas) stoves and generally on electrical appliances such as printers.

• • Bereich Appliance: Fixierung beweglicher Teile von Kühl- und Gefriergeräten und anderer Haushaltsgeräte wie Gasherde etc.
• • Bereich Office Automation: Fixierung beweglicher Teile von Druckern, Kopiergeräten etc.

In technical jargon, the areas are designated as follows:

• • Appliance area: fixation of moving parts of refrigerators, freezers and other household appliances such as gas stoves etc.
• • Office Automation: Fixing moving parts of printers, copiers, etc.

1. a) die temporäre Fixierung von größeren Bauteilen wie zum Beispiel Windschutzscheiben von Autos nach dem Einsetzen in den Rahmen bis zur Aushärtung des PU-Flüssigklebers, um ein Verrutschen während des Aushärteprozesses zu verhindern,
2. b) das so genannte Endtabbing (Endlagenverklebung) von Metall-Coils mit dem Anspruch der rückstandsfreien Wiederablösbarkeit auch bei niedrigen Temperaturen,
3. c) das temporäre Verschließen von Behältern oder generelles Bekleben von Oberflächen mit der Anforderung auf rückstandsfreie Wiederablösbarkeit auch bei niedrigen Temperaturen.

Other applications of such adhesive tapes are

1. a) the temporary fixation of larger components such as windshields of cars after insertion into the frame to the curing of the PU liquid adhesive to prevent slippage during the curing process,
2. b) the so-called Endtabbing (Endlagenverklebung) of metal coils with the claim of residue-free removability even at low temperatures,
3. c) the temporary closing of containers or general bonding of surfaces with the requirement for residue-free removability even at low temperatures.

The residue-free removability (removability) of a (strapping) tape from different substrates depends essentially on the pull-off forces that develop after different periods of time when removing the tape from the respective substrates. Ideally, the peel force increases only slightly or even not at all as compared to the initial one, since with increasing pull-off force the risk increases that either the wearer tears or residues remain behind. Thus, the film carrier may fail in the case of excessive forces and tear and / or splice. Further results of high peel forces can be either the cohesive splitting of the adhesive or also the adhesive failure of the composition by detachment from the support.

In all cases, unwanted residues of the adhesive tape on the substrate, be it in the form of parts of the tape itself or parts of the adhesive.

There is a need for a strapping tape that can be used universally on all substrates relevant to the application, such as the plastics ABS, PS, PP, PE, PC, POM, such as various metals, such as solvent, water-based and applied as a powder paints and other solvent-free paints (for example, UV-curing paints), which at the same time adheres to these substrates with sufficiently high bond strengths of usually at least 2.5 N / cm, but still without residue and damage even after prolonged storage at different temperatures (temperature range: -20 ° C to +60 ° C) and UV irradiation can be removed.

Although strapping tapes are used in a wide variety of applications, they have some essential properties to meet the particular requirements placed on them. These are - without this list claims to be exhaustive - a very high tensile strength (maximum tensile strength), a very good tensile strength corresponding to a high modulus at low strains and a low elongation at break, a sufficient but not too high bond strength, a metered bond strength on the own backside, the residue-free redetachability after the stresses of the actual application, the robustness of the wearer against mechanical stress and for some applications also the resistance of the adhesive tape against UV radiation and against many chemicals.

While some of the properties are due to the adhesive or other functional layers of the adhesive tape, the extensibility and tensile strength are essentially based on the physical properties of the support material used.

It should not go unmentioned at this point, another disadvantage of the increased bond strength of strapping tapes. This is because with the increase in bond strength also increases the risk of damaging the substrate during removal, for example by lifting paint coatings.

Especially in the case of rapid removal in unfavorable, but occurring in practice acute angles may occur in strapping tapes already at speed-dependent adhesive forces of more than about 3 N / cm, that the adhesive tape carrier breaks and splits in the z direction, the so-called shredding. At the same time, such adhesive forces also make increased demands on the effectiveness of the primer or on the anchoring of the adhesive on the film carrier and on the cohesion of the composition. The problem is aggravated at low temperatures of less than 0 ° C. Even at these low temperatures, the tape must not show any shredding.

• • Das Klebeband muss lose Teile während des Transports sichern, das heißt, das Klebeband sollte eine hohe Reißfestigkeit in Maschinenrichtung und ausreichende Klebkräfte aufweisen.
• • Das Klebeband darf sich unter Belastung nicht stark dehnen, das heißt, das Klebeband sollte - sofern ermittelbar -- hohe F5%-Werte [hohe Werte der Zugfestigkeit bei 5 %-Dehnung] beziehungsweise ein hohes E-Modul aufweisen.
• • Das Klebeband muss unter verschiedenen klimatischen Bedingungen funktionieren, das heißt, das Klebeband sollte eine Klimabeständigkeit im Temperaturbereich zwischen -20 °C bis 40 °C und einer relativen Luftfeuchte von bis zu 95 % aufweisen.
• • Das Klebeband sollte wiederabziehbar im Temperaturbereich zwischen -20 °C bis 40 °C und einer relativen Luftfeuchte von bis zu 95 % sein.
• • Das Klebeband sollte wärmebeständig beim Trocknen der Klebstoffbeschichtung im Herstellprozess des Klebebandes sein.
• • Das Klebeband sollte leicht zu verwenden sein, das heißt, das Klebeband sollte vorzugsweise eine geringe Abrollkraft aufweisen, was insbesondere über die Verwendung eines Carbamat- oder Silikon-Releases sichergestellt werden kann.
• • Das Klebeband sollte auf verschiedenen Haftgründen gut kleben und ausreichend Kohäsion haben, um das Transportgut zu sichern, das heißt, das Klebeband kann eine Klebmasse auf Basis Naturkautschuk, SIS-Kautschuk oder Acrylat aufweisen.

An adhesive tape which is to be used as a (strapping) adhesive tape should therefore have the following properties:

• • The tape must secure loose parts during transport, ie the tape should have a high tear strength in the machine direction and sufficient bond strength.
• • The adhesive tape must not stretch strongly under load, ie the adhesive tape should, if possible, have high F5% values [high tensile strength values at 5% elongation] or a high modulus of elasticity.
• • The tape must work under different climatic conditions, ie the tape should have a climatic resistance in the temperature range between -20 ° C to 40 ° C and a relative humidity of up to 95%.
• • The tape should be removable in the temperature range between -20 ° C to 40 ° C and a relative humidity of up to 95%.
• • The tape should be heat resistant when drying the adhesive coating in the tape manufacturing process.
• The adhesive tape should be easy to use, that is, the adhesive tape should preferably have a low unwind force, which can be ensured in particular by using a carbamate or silicone release.
• • The adhesive tape should adhere well to various adhesion reasons and have sufficient cohesion to secure the goods to be transported, ie the adhesive tape may have an adhesive based on natural rubber, SIS rubber or acrylate.

1. i) Biaxial orientierte PET-Folien mit einer Dicke zwischen 30 und 60 µm
2. ii) Monoaxial orientierte PP-Folien mit einer Dicke zwischen 40 und 150 µm

The prior art includes tapes, which are used in the field of strapping (bundling), appliance (transport security of moving parts such as drawers, shelves, flaps especially in household appliances, etc.) and in the furniture industry and when used for other applications weaknesses in removing the tape from Substrate in the lower temperature range (below approx. 10 ° C). There are mainly two different films used for strapping tapes as backing materials:

1. i) Biaxially oriented PET films with a thickness of between 30 and 60 μm
2. ii) monoaxially oriented PP films having a thickness of between 40 and 150 μm

Biaxially stretched PET supports are known to be advantageous over monoaxially drawn PP supports (MOPP) due to their higher cold cracking resistance, but earlier tear machine direction (MD) than MOPP, are more expensive and colorless in the marketplace. A coloring of the adhesive tape based on a PET film takes place via a subsequent printing process or coloring of the adhesive. Monoaxially stretched PP films, on the other hand, are cheaper and easily dyeable (easily recognizable), which is a general requirement for adhesive tapes that are to be removed again. Both types of films are due to the high modulus of elasticity under tensile load in the application little stretchy, so well suited. MOPP strapping tapes are typically used to wrap palletized cartons; the film does not split when peeled because the paper easily splits on the surface. Up until now, it has only been possible to use MOPP film for surface-protection adhesive tapes if the adhesive adheres so weakly that no adhesive or residual tape with film content remains. There is therefore a need to provide an adhesive tape for surface protection applications, for example, as a transport lock for PC printers, refrigerators, electric and gas stoves or furniture available, which has a high adhesion, but is removable without residue and in particular below usual Room temperature, for example between -20 ° C and +7 ° C. As the temperature decreases, the toughness of a polypropylene film decreases and at the same time the adhesive strength of the adhesive increases. The challenge is to minimize this behavior in the cold and to find a solution to the technical problem by a suitable combination of film and adhesive.

Many of the known strapping tapes have a monoaxially stretched polypropylene (MOPP) backing since MOPP in the machine direction (MD) has a very high power input. Due to the stretching in the machine direction (x direction, MD), the toughness of the MOPP carrier decreases in the y direction (transverse direction, CD (cross direction)) and z direction (in the z direction the thickness of the film is determined) This makes the internal strength of the MOPP a weak point. Consequently, the carrier frayed and remain the adhesive and film residues on the ground back, which is a frequent complaint reason.

The weak point of MOPP is the low strength in the cross-machine direction (CD) and inside the film in the z-direction. This effect increases at lower temperatures (-20 ° C), since the glass transition temperature of polypropylene (between 0 and -20 ° C) is reached or fallen below and the carrier is very brittle. This effect is particularly pronounced when using a PP homopolymer, since the regular arrangement of the polymer chains results in a high degree of crystallinity which makes the film very strong, stiff and brittle. Especially for applications at low temperatures, there are heterophasic PP copolymers in which an ethylene-propylene copolymer (EP phase) is finely dispersed mixed or polymerized in the PP homopolymer matrix. The present EP phase increases the toughness of the PP copolymer.

Heterophasic polypropylenes or polypropylenes having different phases, in particular propylene copolymers having different phases, ie polymers containing a propylene polymer matrix and an elastomer, are known.

It is known to use a softer carrier. Polyethylene is added as standard to lower the glass transition temperature and maintain greater flexibility of the support at lower temperatures. This improves the tendency to fray at lower temperatures, but can not be completely eliminated. A disadvantageous effect here is a reduction in the strength of a corresponding film. In order to offer a robust and shredding-free solution, an adhesive with lower bond strengths at low temperatures is used on the adhesive tape. However, as the market demands higher bond strengths at low temperatures to ensure transport safety, another carrier must be chosen.

A common problem with MOPP films, in addition to shredding when removing the tape, is the appearance of fibers during the cutting and finishing process. The fibers formed have a strong influence on process safety, production speed and product quality. Fiber-free films can increase production speed by at least 100%, if not 400% or more. Furthermore, the process becomes more efficient; since complex cleaning accounts. If an optical fault detection system is used in production, the occurrence of fibers and fiber agglomerates often leads to the triggering of fault detection and thus to stoppages in the production process.

The object of the invention is to achieve a significant improvement over the prior art and to provide a film for an adhesive tape and the adhesive tape itself, which has a reduced splitting when removing the adhesive tape in the cold at a temperature range between -20 ° C. and to +7 ° C, in particular, the cold gap strength in the transverse and z-direction is to be improved with jerky load on the wearer.

This object is achieved by an adhesive tape, as characterized in detail in the main claim. Advantageous embodiments of the invention are described in the subclaims. Furthermore, the invention comprises the film which is suitable as a carrier in the adhesive tape.

1. i) 80 bis 99 Gew.-%, vorzugsweise 93 bis 96 Gew.-%, auf das Gesamtgewicht der Komponenten i) und ii) bezogen, einer Propylenpolymermatrix, die ein Propylenhomopolymer und weiter vorzugsweise ein bevorzugt statistisches Propylencopolymer umfasst, das ein Comonomer aufweist, das aus Ethylen und C₄- bis C₁₀-α-Olefinen ausgewählt ist, wobei die Propylenpolymermatrix einen Comonomergehalt von nicht mehr als 15 Gew.-% aufweist;
2. ii) 1 bis 20 Gew.-%, vorzugsweise 4 bis 7 Gew.-%, auf das Gesamtgewicht der Komponenten i) und ii) bezogen, eines Elastomers in Form eines Ethylen-Propylen-Copolymers mit einem Ethylengehalt von 50 bis 90 Gew.-%.

Accordingly, the invention relates to an adhesive tape with a carrier with a film, to which at least one side an adhesive is applied, and the film itself, wherein the film is a monoaxially (in the machine direction) stretched film which is at least 95 wt .-%, preferably at 99% by weight, more preferably at 100% by weight, of a propylene polymer composition having different phases, comprising the following components:

1. i) 80 to 99% by weight, preferably 93 to 96% by weight, based on the total weight of components i) and ii) of a propylene polymer matrix comprising a propylene homopolymer and more preferably a preferably random propylene copolymer having a comonomer selected from ethylene and C ₄ to C ₁₀ α-olefins, the propylene polymer matrix having a comonomer content of not more than 15% by weight;
2. ii) 1 to 20 wt .-%, preferably 4 to 7 wt .-%, based on the total weight of components i) and ii), of an elastomer in the form of an ethylene-propylene copolymer having an ethylene content of 50 to 90 wt. -%.

The 100 wt.% Missing portions in the film may consist of the later mentioned components to be added to the propylene polymer composition.

More preferably, the propylene polymer composition consists only of components i) and ii). Other polymers are then not included in the matrix.

The propylene polymer matrix (component i) may comprise a pure propylene homopolymer or preferably a mixture of propylene homopolymer and of a preferably random propylene copolymer, preferably of the propylene homopolymer or of this mixture. The blend of propylene homopolymer and a propylene random random copolymer is known as heterophasic propylene copolymer (also known as impact polypropylene).

According to a particularly advantageous embodiment, the proportions of propylene homopolymer and propylene copolymer in the propylene polymer matrix are distributed as follows: 70 to 99% by weight Propylene homopolymer and 1 to 30% by weight propylene copolymer

The propylene polymer matrix according to a preferred variant has a melt flow index MFI of 0.5 to 5 g / 10 min (measured according to ISO 1133 at 230 ° C and under a weight of 2.16 kg), preferably 1 to 5 g / 10 min Mol weight M _w of 500,000 to 1,000,000 g / mol and a bending modulus of 1000 to 1300 MPa.

The matrix polymer preferably contains at least two polypropylenes. If the matrix polymer comprises more different propylene polymers, these polymers can have different molecular weight distributions. These components may have identical or different tacticity.

The matrix polymer may be produced in a polymerization step conducted in one or more polymerization reactors or by blending two or more compatible polymers having the desired molecular weight distribution or monomer composition. Desirably, a matrix polymer comprising two or more different propylene polymers can be prepared by the use of two or more types of catalysts in one polymerization in one reactor, or alternatively by carrying out the polymerization in two or more different polymerization reactors (e.g., bulk, suspension, and / or or gas phase reactors, closed loop reactors being preferred as mass reactors) to produce matrix polymers having the desired different molecular weight distribution or monomer composition in the various polymerization reactors. The latter method is preferred.

The matrix preferably consists of a propylene homopolymer and a preferably random propylene copolymer. The comonomers are selected from ethylene and C ₄ to C ₁₀ α-olefins. Particular preference is given to choosing ethylene as the comonomer. The comonomer content (based on the propylene polymer matrix (component i)), preferably ethylene content, is up to 15% by weight, preferably 3 to 8% by weight. Most preferably, the propylene polymer matrix (component i) consists of a heterophasic propylene copolymer (also known as impact polypropylene).

According to the invention, the term homopolymer is used to denote a polymer in which at least 99% by weight is derived from a single monomer and the polymer chain has a high isotacticity of at least 95%.

The preparation of polymers having the desired properties for the components of the matrix polymer can be achieved by using techniques well known to those skilled in the art, for example, by appropriate selection of catalyst systems (for example, Ziegler-Natta catalysts or metallocene or other uniformly-active catalysts Centers), the comonomers, the type of polymerization reactor and the conditions of the polymerization process. Most preferably, the matrix polymer is prepared in a polymerization process employing a supported Ziegler-Natta catalyst system (particularly, a high yield Ziegler-Natta system containing Ti, Cl, Mg, and Al). Metallocene catalysts can also be used.

The second component (component ii)) of the different phase polymer composition of the present invention is the elastomer in the form of an ethylene-propylene copolymer having an ethylene content of 50 to 90% by weight.

Ethylene-propylene elastomers also known as ethylene-propylene rubber, EPM or EPR, there is today in a wide range of variations. Typically, the ethylene-propylene elastomers have an ethylene content of 45 to 80 weight percent, are available in a wide viscosity or molecular weight range, and may contain as a further monomer a diene monomer (subsequently vulcanizable as EPDM). The ethylene-propylene rubbers may be amorphous and partially crystalline. This depends on the ethylene-propylene content in the polymer. In the range of 45 to 55 weight percent ethylene, an amorphous, noncrystalline polymer is present. From a proportion of greater than 65 wt .-% of ethylene, it comes to the formation of pronounced ethylene crystallites. The preparation of the ethylene-propylene rubbers is typically carried out in the solvent, suspension (also called slurry process) and gas phase process using Ziegler-Natta catalysts or, more rarely, using metallocene catalysts.

According to a preferred embodiment of the invention, the ethylene content of component ii) is 55 to 80 wt .-% and particularly preferably 65 to 75 wt .-%.

Further preferably

• • the value for the modulus of elasticity is 25 to 150 MPa,
• • the softening point is less than 70 ° C (measured according to DSC),
• • the melt flow index MFI is less than 10 g / 10 min, preferably less than 5 g / 10 min (measured according to ISO 1133 at 190 ° C and under a weight of 2.16 kg) and / or
• • the degree of crystallinity α is equal to 0.1

As with the matrix polymer, the elastomer may be prepared by conventional gas phase polymerization techniques. However, it is preferably prepared using a supported catalyst system, for example a Ziegler-Natta catalyst system or a metallocene alumoxane catalyst system.

The elastomer (component ii)) can be mixed with the matrix polymer (component i)). This mixing or blending of the two components can advantageously be carried out directly in the melt-down extruder for producing the polymer film. For this purpose, a single-screw extruder will usually be used. However, the mixing of the components can also take place in a separate step, for example with the aid of a twin-screw extruder.

1. a) Polymerisieren von Propylen in einem ersten Reaktor, wodurch ein erstes Homopolymer erzeugt wird;
2. b) weiteres Polymerisieren von Propylen und einem Comonomer, das aus insbesondere Ethylen und C₄- bis C₁₀-α-Olefinen ausgewählt ist, in einem weiteren Reaktor in Gegenwart des ersten Polymers, wodurch ein Gemisch aus dem ersten Polymer und einem zweiten Polymer erzeugt wird;
3. c) Mischen oder Blenden oder eine Kombination aus Mischen oder Blenden von Komponente i) aus a) + b) mit einem Elastomer (Komponente ii)) in Form eines Ethylen-Propylen-Copolymers mit einem Ethylengehalt von 50 bis 90 Gew.-%, bevorzugt 55 bis 80 Gew.-% und besonders bevorzugt 65 bis 75 Gew.-%.

According to a preferred embodiment, the composition according to the invention is prepared by a process comprising the following steps:

1. a) polymerizing propylene in a first reactor, thereby producing a first homopolymer;
2. b) further polymerizing propylene and a comonomer selected from in particular ethylene and C ₄ to C ₁₀ α-olefins in another reactor in the presence of the first polymer, thereby producing a mixture of the first polymer and a second polymer becomes;
3. c) mixing or blending or a combination of blending or blending of component i) from a) + b) with an elastomer (component ii)) in the form of an ethylene-propylene copolymer having an ethylene content of 50 to 90% by weight, preferably 55 to 80 wt .-% and particularly preferably 65 to 75 wt .-%.

In steps a) and b) of this process, in which the propylene polymer matrix is produced, the polymerizations are preferably carried out in mass reactors (for example closed-loop reactors), slurry reactors, or gas-phase reactors.

An overview of suitable manufacturing processes can be found in Ullmann's "Encyclodedia of Industrial Chemistry", keyword "Polypropylene" by M. Gahleitner and C. Paulik, Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim 2014 (Number 10.1002 / 14356007.o21_o04.pub2).

In addition to the matrix polymer component i) and the elastomer component ii), the polymer composition according to the invention may contain other components, for example conventional additives such as dyes, nucleating agents, fillers, antioxidants, radiation stabilizers, processing aids, etc. The use of inorganic, organic or polymeric nucleating agents particularly preferred. Preferably, said additives are used in an additional polymer as a masterbatch.

The polymer composition of the present invention can be prepared for use by mixing the components preferably in an extruder. The mixing or blending of components i) and ii) and of the additional components can advantageously be carried out directly in the melt-down extruder for producing the polymer film. For this purpose, a single-screw extruder will usually be used. However, the mixing of the components can also take place in a separate step, for example with the aid of a twin-screw extruder.

The film of the adhesive tape according to the invention is obtained by extrusion and stretching in the longitudinal direction using conventional, generally known methods.

The stretch ratio in the stretching of the extruded primary film in the longitudinal direction (machine direction) is preferably 1: 5 to 1: 9, particularly preferably 1: 6 to 1: 8. A stretch ratio of 1: 6 indicates that a section of 6 m length of the stretched film is formed from a section of the film of, for example, 1 m in length. The stretching takes place without the width of the primary film substantially decreasing, mainly at the expense of the thickness of the film.

The usual film thickness after stretching is between 40 and 150 microns. Preferred are 50 to 100 microns.

The monoaxially stretched film of components i) and ii) according to the invention is characterized by a degree of crystallization α of 0.4 to 0.5.

As a rule, at least one corona or else flame pretreatment of the side of the film carrier to be coated later with the adhesive takes place in order to better anchor the adhesive to the carrier. A further improvement in adhesion equivalent to the anchoring of the adhesive on the support can be achieved by the use of primers. With these, on the one hand, the surface energy can be adjusted in a targeted manner and, on the other hand, for example when using isocyanate-containing primers, a chemical attachment of the elastomeric adhesive component to the carrier can be pursued.

The usual surface application weight of the primer is between 0.1 and 10 g / m ² . Another way to improve the anchoring, is the use of carrier films, which are equipped by coextrusion at the film manufacturer specifically with a favorable for the connection to the pressure sensitive adhesive polymer surface.

Descriptions of the adhesives and release coatings and primers commonly used for adhesive tapes can be found, for example, in Donatas Satas' Handbook of Pressure Sensitive Adhesive Technology (van Nostrand, 1989).

Preferably, the adhesive applied to the carrier material is a pressure-sensitive adhesive, that is to say an adhesive which, even under relatively weak pressure, permits a permanent connection with almost all adhesive reasons and can be detached again from the primer after use essentially without residue. A PSA is permanently tacky at room temperature, so it has a sufficiently low viscosity and high tack, so that it wets the surface of the respective Klebegrunds already at low pressure. The adhesiveness of the adhesive is based on its adhesive properties and the removability on their cohesive properties.

In order to produce a likewise inventive adhesive tape from the film according to the invention, all known adhesive systems can be used. In addition to the preferred adhesives based on natural or synthetic rubber, it is possible to use silicone adhesives and also polyacrylate adhesives, preferably a low molecular weight acrylate hot melt pressure-sensitive adhesive.

Preferably, an adhesive is used which consists of the group of natural rubbers or of any blend of natural rubbers and / or synthetic rubbers, wherein the proportion of the synthetic rubber in the blend according to a preferred variant is at most as large as the proportion of natural rubber.

Rubber adhesives show a good combination of bond strength, tack and cohesion as well as balanced adhesion on almost all relevant substrates and are thus predestined. General information on rubber adhesives can be found, inter alia, in standard works for adhesive tapes such as, for example, the "Handbook of Pressure Sensitive Adhesive Technology" by Donatas Satas.

The natural rubber or natural rubbers can in principle be made of all available grades such as Crepe, RSS, ADS, TSR or CV grades, depending on the required level of purity and viscosity, and the synthetic rubber or synthetic rubbers from the group of random copolymerized Styrene butadiene rubbers (SBR), butadiene rubbers (BR), synthetic polyisoprenes (IR), butyl rubbers (IIR), halogenated butyl rubbers (XIIR), acrylate rubbers (ACM), ethylene oxide Vinyl acetate copolymers (EVA) and the polyurethanes and / or their blends are selected.

Further, it is preferable to add to the rubbers, for the purpose of improving the processability, thermoplastic elastomers having a weight proportion of 10 to 50% by weight, based on the total elastomer content.

Representative may be mentioned at this point especially the most compatible styrene-isoprene-styrene (SIS) - and styrene-butadiene-styrene (SBS) types. Suitable elastomers for blending are also, for example, EPDM or EPM rubber, polyisobutylene, butyl rubber, ethylene-vinyl acetate, hydrogenated block copolymers of dienes (for example by hydrogenation of SBR, cSBR, BAN, NBR, SBS, SIS or IR, such polymers for example known as SEPS and SEBS) or acrylate copolymers such as ACM.

In addition, a 100% system based on styrene-isoprene-styrene (SIS) has proven suitable.

Crosslinking is advantageous for improving the redetachability of the adhesive tape after use and may be thermal or by exposure to UV light or electron beams.

For the purpose of thermally induced chemical crosslinking, all known thermally activatable chemical crosslinkers such as accelerated sulfur or sulfur donor systems, isocyanate systems, reactive melamine, formaldehyde and (optionally halogenated) phenol-formaldehyde resins or reactive phenolic resin or Diisocyanatvernetzungssysteme with the corresponding activators, epoxidized polyester - And acrylate resins and their combinations used.

The crosslinkers are preferably activated at temperatures above 50 ° C, in particular at temperatures of 100 ° C to 160 ° C, most preferably at temperatures of 110 ° C to 140 ° C.

The thermal excitation of the crosslinker can also be effected by IR radiation or high-energy alternating fields.

Suitable adhesives are solvent-based, water-based or even as a hot-melt system. A composition based on acrylate hotmelt is also suitable, it being possible for it to have a K value of at least 20, in particular greater than 30, obtainable by concentrating a solution of such composition into a system which can be processed as a hotmelt.

The concentration can take place in suitably equipped boilers or extruders, in particular in the concomitant degassing a vented extruder is preferred.

Such an adhesive is in the DE 43 13 008 A1 , the contents of which are hereby incorporated by reference and the content of which will become part of this disclosure and invention.

The adhesive on Acrylathotmelt-based but can also be chemically crosslinked.

In a further embodiment, self-adhesives used are copolymers of (meth) acrylic acid and their esters having 1 to 25 C atoms, maleic, fumaric and / or itaconic acid and / or their esters, substituted (meth) acrylamides, maleic anhydride and other vinyl compounds, such as vinyl esters, in particular vinyl acetate, vinyl alcohols and / or vinyl ethers used.

The residual solvent content should be below 1% by weight.

An adhesive which also shows to be suitable is a low molecular weight acrylate hot melt pressure-sensitive adhesive, such as that which is marketed under the name acResin UV or Acronal®, in particular Acronal® DS 3458, by BASF. This adhesive with a low K value obtains its application-oriented properties through a final radiation-induced crosslinking.

Finally, it should be mentioned that adhesives based on polyurethane or polyolefin are also suitable.

To optimize the properties, the self-adhesive composition used can be blended with tackifiers (resins) and / or one or more additives such as plasticizers, fillers, pigments, UV absorbers, light stabilizers, aging inhibitors, crosslinking agents, crosslinking promoters or elastomers.

By the term "tackifier resin", the skilled person understands a resin-based substance which increases the tackiness.

Tackifiers are, for example, in particular hydrogenated and nonhydrogenated hydrocarbon resins (for example from unsaturated C ₅ or C ₇ monomers), terpene phenolic resins, terpene resins from raw materials such as α- or β-pinene and / or δ-lime, aromatic resins such as coumarone Indene resins or resins of styrene or α-methylstyrene such as rosin and its derivatives such as disproportionated, dimerized or esterified resins, whereby glycols, glycerol or pentaerythritol can be used. Particularly suitable are age-stable resins without olefinic double bond such as hydrogenated resins.

The presentation of the state of knowledge in the "Handbook of Pressure Sensitive Adhesive Technology" by Donatas Satas (van Nostrand, 1989) is expressly pointed out.

The adhesive may be added to stabilize conventional additives such as anti-aging agents (antiozonants, antioxidants, sunscreens, etc.).

• • Plastifizierungsmittel wie zum Beispiel Weichmacheröle oder niedermolekulare flüssige Polymere wie zum Beispiel niedermolekulare Polybutene
• • primäre Antioxidantien wie zum Beispiel sterisch gehinderte Phenole
• • sekundäre Antioxidantien wie zum Beispiel Phosphite oder Thiosynergisten (Thioether)
• • Prozessstabilisatoren wie zum Beispiel C-Radikalfänger
• • Lichtschutzmittel wie zum Beispiel UV-Absorber oder sterisch gehinderte Amine
• • Verarbeitungshilfsmittel
• • Netzadditive
• • Haftvermittler
• • Endblockverstärkerharze und/oder
• • gegebenenfalls weitere Polymere von bevorzugt elastomerer Natur; entsprechend nutzbare Elastomere beinhalten unter anderem solche auf Basis reiner Kohlenwasserstoffe, zum Beispiel ungesättigte Polydiene wie natürliches oder synthetisch erzeugtes Polyisopren oder Polybutadien, chemisch im wesentlichen gesättigte Elastomere wie zum Beispiel gesättigte Ethylen-Propylen-Copolymere, α-Olefincopolymere, Polyisobutylen, Butylkautschuk, Ethylen-Propylenkautschuk, sowie chemisch funktionalisierte Kohlenwasserstoffe wie zum Beispiel halogenhaltige, acrylathaltige, allyl- oder vinyletherhaltige Polyolefine
• • Füllstoffe wie Fasern, Ruß, Zinkoxid, Titandioxid, Mikrovollkugeln, Voll- oder Hohlglaskugeln, Kieselsäure, Silikaten, Kreide

As additives to the adhesive are typically used:

• Plasticizers such as plasticizer oils or low molecular weight liquid polymers such as low molecular weight polybutenes
• • primary antioxidants such as sterically hindered phenols
• • secondary antioxidants such as phosphites or thiosynergists (thioethers)
• • Process stabilizers such as C radical scavenger
• • Sunscreens such as UV absorbers or hindered amines
• • processing aids
• • Net additives
• • bonding agent
• • End block booster resins and / or
• Optionally further polymers of preferably elastomeric nature; correspondingly useful elastomers include, but are not limited to those based on pure hydrocarbons, for example, unsaturated polydienes such as natural or synthetically produced polyisoprene or polybutadiene, chemically substantially saturated elastomers such as saturated ethylene-propylene copolymers, α- Olefincopolymere, polyisobutylene, butyl rubber, ethylene-propylene rubber, and chemically functionalized hydrocarbons such as halogen-containing, acrylate-containing, allyl or vinyl ether-containing polyolefins
• • Fillers such as fibers, carbon black, zinc oxide, titanium dioxide, micro-solid spheres, solid or hollow glass spheres, silica, silicates, chalk

Examples of suitable fillers and pigments are fibers, carbon black, zinc oxide, titanium dioxide, micro-solid spheres, solid or hollow glass spheres, silica, silicates, carbon black, titanium dioxide, calcium carbonate and / or zinc carbonate.

Suitable anti-aging agents (antiozonants, antioxidants, light stabilizers, etc.) for the adhesives are primary antioxidants such as sterically hindered phenols, secondary antioxidants such as phosphites or thiosynergists (thioethers) and / or light stabilizers such as UV absorbers or hindered amines.

Suitable plasticizers are, for example, aliphatic, cycloaliphatic and aromatic mineral oils, di- or poly-esters of phthalic acid, trimellitic acid or adipic acid, liquid rubbers (for example nitrile or polyisoprene rubbers), liquid polymers of butene and / or isobutene, acrylic esters, polyvinyl ethers, liquid and soft resins based on the raw materials to adhesive resins, wool wax and other waxes or liquid silicones.

Crosslinking agents are, for example, phenolic resins or halogenated phenolic resins, melamine and formaldehyde resins. Suitable crosslinking promoters are, for example, maleimides, allyl esters, such as triallyl cyanurate, polyfunctional esters of acrylic and methacrylic acid.

The enumerated substances are in turn not mandatory, the adhesive also works without these added individually or in any combination, ie without resins and / or residual additives.

The coating thickness with adhesive is preferably in the range from 1 to 100 g / m ² , in particular from 10 to 50 g / m ² , more preferably in the range from 15 to 35 g / m ² .

The preparation and processing of the PSAs can be carried out from solution, dispersion and from the melt. Preferred production and processing methods are carried out from solution or dispersion.

The pressure-sensitive adhesives prepared in this way can then be applied to the carrier by the generally known methods. When processed from the melt, these can be application methods via a nozzle or a calender.

In solution processes, coatings with doctor blades, knives or nozzles are known, to name just a few.

The adhesive in conjunction with said film allows in the range of the usual application temperature, which is between -20 ° C and +40 ° C, a residue-free peeling.

For the purposes of this invention, the general term "adhesive tape" encompasses all flat structures such as films or film sections which are expanded in two dimensions, tapes of extended length and limited width, strip sections and the like, and ultimately also diecuts or labels.

The adhesive tape can be rolled up on itself in the form of a roll, that is to say in the form of an Archimedean spiral, and also produced with adhesive materials such as siliconized paper or siliconized film.

As a release material is preferably a non-fluffing material such as a plastic film or a well-glued, long-fiber paper.

The adhesive tapes have in particular run lengths of 1,000 to 30,000 m.

On the back of the adhesive tape, a backside lacquer can be applied to favorably influence the unwinding properties of the adhesive tape wound on the Archimedean spiral. This backcoat can be used with silicone or fluorosilicone compounds as well as with polyvinyl stearyl carbamate, Polyethyleniminstearylcarbamid or fluoroorganic compounds as abhesive (anti-adhesive) substances to be equipped.

Suitable release agents include surfactant release systems based on long chain alkyl groups such as stearylsulfosuccinates or stearylsulfosuccinamates, but also polymers which may be selected from the group consisting of polyvinyl stearyl carbamates, polyethyleneimine stearyl carbamides, chromium complexes of C ₁₄ to C ₂₈ fatty acids and stearyl copolymers such as for example in DE 28 45 541 A are described. Also suitable are release agents based on acrylic polymers with perfluorinated alkyl groups, silicones or fluorosilicone compounds, for example based on poly (dimethyl-siloxanes). Most preferably, the release layer comprises a silicone-based polymer. Particularly preferred examples of such silicone-based release polymers include polyurethane- and / or polyurea-modified silicones, preferably organopolysiloxane / polyurea / polyurethane block copolymers, more preferably those as in Example 19 of EP 1 336 683 B1 very particularly preferably anionically stabilized polyurethane- and urea-modified silicones having a silicone weight fraction of 70% and an acid number of 30 mg KOH / g. The use of polyurethane and / or urea-modified silicones causes the effect that the products according to the invention have an optimized separation behavior with optimized aging resistance and universal writability. In a preferred embodiment of the invention, the release layer comprises 10 to 20% by weight, particularly preferably 13 to 18% by weight, of the release-active constituent.

Adhesive tapes according to the invention are preferably used in the widths of 9 to 50 mm, in particular 19 to 25 mm, and in this case have a preferred thickness of 40 to 200 μm, preferably 70 to 180 μm, more preferably 75 to 120 μm.

The width of the rolls is usually 10, 15, 19, 25 and 30 mm.

In the 1 a typical construction of the adhesive tape according to the invention is shown.

The product consists of a film (a) and an adhesive (b). In addition, it is also possible to use a primer (c) for improving the adhesion between the adhesive and the backing and a reverse side release (d).

The carrier (a) consists of a monoaxially oriented polypropylene film with a preferred thickness between 40 and 150 microns.

The adhesive (b) is a mixture of natural rubber or other elastomers and various resins and may optionally also contain plasticizers, fillers and anti-aging agents.

The preparation and processing of the PSAs can be carried out from solution, dispersion and from the melt. Preferred production and processing methods are carried out from solution as well as from the melt. Particularly preferred is the production of the adhesive from the melt, in particular batch or continuous processes can be used. Particularly advantageous is the continuous production of the PSAs by means of an extruder.

The pressure-sensitive adhesives prepared in this way can then be applied to the carrier by the generally known methods. When processed from the melt, these can be application methods via a nozzle or a calender.

In solution processes, coatings with doctor blades, knives or nozzles are known, to name just a few.

Heterophasic PP copolymer is intended for use at lower temperatures, as the material retains a certain degree of flexibility due to the built-in EP phase, even at low temperatures, and has a higher toughness than PP homopolymers or PP random copolymers. A weak point of the heterophasic PP copolymers is the rather poor binding of the EP phase to the PP homopolymer phase, since these two phases are immiscible and thus coexist. When removing the adhesive tape, the weakest point is thus in the connection between the two polymer phases (EP and PP Homo), so that it comes to shredding within the film. The addition of the EPM with low Young's modulus (modulus of elasticity, tensile test) and high ethylene content already in the EP phase increases the ethylene content in the material. Thus, the glass transition temperature is shifted to lower temperatures and the material has at lower Temperatures a higher toughness. Furthermore, the crystallinity in the PP homo-matrix is disturbed, so that there is a higher proportion of amorphous regions, which brings about a higher flexibility. The effect of the elastomer is the reduction of the crystalline portion in the film and "sticking" of the fibrils resulting from the stretching of the amorphous phase in the machine direction (reduction of the post-crystallization of the amorphous phase).

Surprisingly, in the film according to the invention, the strength in the z-direction and fiber formation is significantly improved, especially in the cold, or the shredding is reduced, without reducing the modulus of elasticity or force at 5% elongation, the most important property for MOPP films.

The adhesive tape according to the invention shows good removability from a wide variety of substrates at temperatures of up to -20.degree. On the other hand, however, even at positive temperatures (+40 ° C) the redetachability is given, that is, there are no residues due to cohesive failure of the adhesive, Masseumspulen (poor ground anchorage) or a carrier column to observe. The carrier has a sufficient internal strength in all three spatial directions and high impact resistance even in the cold.

Due to the properties described, the adhesive tape can be excellently used as a strapping adhesive tape for bundling and palletizing cardboard boxes and other goods, even at low temperatures.

Furthermore, with the adhesive tape moving parts such as doors, flaps, etc. on printers or refrigerators can be excellently fixed during transport from the manufacturer to the seller or on to the buyer, even at low temperatures.

1. a) Bei der temporären Fixierung von größeren Bauteilen wie zum Beispiel Windschutzscheiben von Autos nach dem Einsetzen in den Rahmen bis zur Aushärtung des PU-Flüssigklebers, um ein Verrutschen während des Aushärteprozesses zu verhindern.
2. b) Beim Endtabbing (Endlagenverklebung) von Metall-Coils mit dem Anspruch der rückstandsfreien Wiederablösbarkeit auch bei niedrigen Temperaturen.
3. c) Beim temporären Verschließen von Behältern oder generelles Bekleben von Oberflächen mit der Anforderung auf rückstandsfreie Wiederablösbarkeit auch bei niedrigen Temperaturen.

Due to the properties described, the adhesive tape according to the invention can also be used advantageously in the following applications:

1. a) For the temporary fixation of larger components such as windshields of cars after insertion into the frame to the curing of the PU liquid adhesive to prevent slippage during the curing process.
2. b) When Endtabbing (Endlagenverklebung) of metal coils with the claim of residue-free removability even at low temperatures.
3. c) For temporary sealing of containers or general bonding of surfaces with the requirement for residue-free redetachability even at low temperatures.

There is a significantly reduced splitting of the support in the cold to observe, in addition, the adhesive tapes are removable without residue.

The invention described here also solves, by the increased internal strength, the fiber formation in the cutting and finishing process.

1. i) 80 bis 99 Gew.-%, vorzugsweise 93 bis 96 Gew.-%, auf das Gesamtgewicht der Komponenten i) und ii) bezogen, einer Propylenpolymermatrix, die ein Propylenhomopolymer und weiter vorzugsweise ein bevorzugt statistisches Propylencopolymer umfasst, das ein Comonomer aufweist, das aus Ethylen und C₄- bis C₁₀-α-Olefinen ausgewählt ist, wobei die Propylenpolymermatrix einen Comonomergehalt von nicht mehr als 15 Gew.-% aufweist;
2. ii) 1 bis 20 Gew.-%, vorzugsweise 4 bis 7 Gew.-%, auf das Gesamtgewicht der Komponenten i) und ii) bezogen, eines Elastomers in Form eines Ethylen-Propylen-Copolymers mit einem Ethylengehalt von 50 bis 90 Gew.-%.

Further, part of the invention is a film wherein the film is a monoaxially (machine direction) stretched film which is at least 95%, preferably 99%, more preferably 100%, by weight of a propylene polymer composition with different phases, comprising the following components:

1. i) 80 to 99% by weight, preferably 93 to 96% by weight, based on the total weight of components i) and ii) of a propylene polymer matrix comprising a propylene homopolymer and more preferably a preferably random propylene copolymer having a comonomer selected from ethylene and C ₄ to C ₁₀ α-olefins, the propylene polymer matrix having a comonomer content of not more than 15% by weight;
2. ii) 1 to 20 wt .-%, preferably 4 to 7 wt .-%, based on the total weight of components i) and ii), of an elastomer in the form of an ethylene-propylene copolymer having an ethylene content of 50 to 90 wt. -%.

Advantageous embodiments of the inventive film not coated with an adhesive are described in detail in the above disclosure.

In the following, the invention in the form of the film and the adhesive tape is explained in more detail by some examples, without wishing to restrict the invention thereby.

Examples

To investigate the advantageous properties of the film, it is necessary to equip them with an adhesive, so to make an adhesive tape. The observed improvements in the behavior of the adhesive tape according to the invention are essentially, if not 100% attributable to the film according to the invention itself.

All amounts, parts and percentages are by weight "GT" means parts by weight.

Experimental Procedure

A dry blend of the heterophasic copolymer with the EPM (preferred concentration 4 to 7% by weight) is prepared and melted with the aid of a single-screw extruder (at temperatures between 160 and 240 ° C.). The melt is formed by a slot die into a film and placed on a chill roll (at temperatures between 60 to 100 ° C) and cooled. With the aid of a monoaxial stretching unit, the film is stretched in the short stretch-splitting method at drawing rates of 1: 5 to 1: 9 (preferably 1: 6 to 1: 8).

The dry blend consists of 5% by weight of the ExxonMobil EPM Vistalon 722 elastomer, an ethylene-propylene copolymer having an ethylene content of 72% by weight, and an MFI (measured at 190 ° C. and 2.16 kg load ) of 1.0 g / 10 min and a modulus of elasticity of 1240 MPa, and of 95% by weight of the heterophasic PP copolymer Profax SV 258 from LyondellBasell, with an MFI (measured at 230 ° C. and 2.16 kg load) of 1.2 g / 10 min and a modulus of elasticity of 1240 MPa. The material is used in a single-screw extruder at temperatures of 180 to. Melted 230 ° C, formed using a slot die to a flat film and placed on a chill roll with a temperature of 95 ° C and cooled. The resulting film has a thickness of 325 microns. After cooling, the film is again heated in a monoaxial stretching unit to temperatures of 127 ° C and drawn in the short-gap with a stretching rate of 1: 6.5 and then annealed at a temperature of 127 ° C and finally wound up. Thus, a final thickness of the film of 50 microns is produced.

Results

When transporting, the mechanical properties of the film are of central importance. A very soft film will probably not have a shredding, but will have a very high elongation at low power consumption. This would cause the film to stretch if forces occur during transport. Thus, the tape would "leach" instead of keeping the cargo together. Table 1: Mechanical properties and shredding results of various MOPP films material F5% [N / mm ² ] F max [N / mm ² ] shredding MOPP film 76 273 Failed Profax SV 258 112 328 Failed Profax SV 258 + 2.5 wt% Vistalon 722 110 328 Failed Profax SV 258 + 5 wt% Vistalon 722 108 317 passed Profax SV 258 + 10 wt% Vistalon 722 103 315 passed

As can be seen in Table 1, the addition of Vistalon 722 lowers the mechanical properties only slightly compared to the pure heterophasic copolymer. At a concentration of 5% by weight, however, the film passes the shredding test. A concentration of 10% by weight of Vistalon has no advantage over 5% by weight of Vistalon, so that a concentration of around 5% by weight is preferred. The to Comparison of tested MOPP film in the tape tesa® 64294, equipped with a natural rubber compound, has a significantly lower power consumption. In addition, the film does not pass the shredding test.

Test Methods

The measurements are (unless otherwise stated) at a test climate of 23 ± 1 ° C and 50 ± 5% rel. Humidity carried out.

shredding

The films are pretreated after 2 weeks of ripening with a corona dose of 60.7 W * min / m ² , at a speed of 30 m / min, in order to increase the surface energy and thus the anchoring to a d / s adhesive tape. The film is laminated to a suitable adhesive tape, for example tesa® 61795 PV40 or tesa® 4965 PV0, and cut into strips 20 mm wide. tesafix® 4965 is a double-sided adhesive, transparent polyester adhesive tape with an acrylate adhesive.

• • Trägermaterial PET-Film
• • Dicke 205,00 µm
• • Klebmasse modifiziertes Acrylat
• • Reißdehnung 50,00 %
• • Reißkraft 20,00 N
• • Klebkraft auf Stahl (initial) 11,50 N/cm
• • Klebkraft auf ABS (initial)
• • 10,30 N/cm Klebkraft auf Aluminium (initial) 9,20 N/cm
• • Klebkraft auf PC (initial) 12,60 N/cm
• • Klebkraft auf PE (initial) 5,80 N/cm
• • Klebkraft auf PET (initial) 9,20 N/cm
• • Klebkraft auf PP (initial) 6,80 N/cm
• • Klebkraft auf PS (initial) 10,60 N/cm
• • Klebkraft auf PVC (initial) 8,70 N/cm

tesa® 4965 has the following properties:

• • Carrier PET film
• • Thickness 205.00 μm
• • Adhesive modified acrylate
• • Elongation at break 50.00%
• • Tensile strength 20.00 N
• • Adhesion to steel (initial) 11.50 N / cm
• • adhesion to ABS (initial)
• • 10,30 N / cm adhesion to aluminum (initial) 9,20 N / cm
• • Adhesive force on PC (initial) 12.60 N / cm
• • Adhesive force on PE (initial) 5.80 N / cm
• • Adhesion to PET (initial) 9.20 N / cm
• • Adhesion to PP (initial) 6.80 N / cm
• • Adhesive force on PS (initial) 10.60 N / cm
• • Adhesive force on PVC (initial) 8,70 N / cm

These composites are then glued to an ethanol-cleaned ABS test plate and stored for 24 hours at room temperature. The film is then removed from the double-sided adhesive tape at three different speeds or angles by hand: slowly at 90 °, slowly at 180 ° and then at 180 °. This test is also carried out after 24 hours storage at -20 ° C. The test is considered to be passed if no film residues remain on the adhesive after the film has been peeled off

Tensile test and modulus of elasticity

According to DIN ISO 527: On a tensile testing machine, a 15 mm wide foil strip is clamped in a jaw distance of 100 mm. The tensile test is carried out at a speed of 300 mm / min until demolition. From the measurement curve, the maximum tensile force Fmax and the force at an elongation of 5% (F5%) are determined. The values are given in N / mm ² , which means that the measured value is normalized to the film thickness. The modulus of elasticity is determined from the force-elongation curve at low elongation according to DIN ISO 527.

crystallinity

The degree of crystallinity is determined by the method as described in the article of Schubnell, M .: "Determination of Crystallinity in Polymers from DSC Measurements"; Mettler Toledo Germany; de.mt.com; USERCOM vol. 1, 2001, pages 12 to 13 , is described.

The degree of crystallinity is determined explicitly by means of a DSC measurement at a heating rate of 10 K / min from the free enthalpy of the 1st heating curve, wherein for the enthalpy of fusion of a 100% crystalline homo-PP, a value of 207 J / g is assumed (literature value ).

adhesive power

The determination of the bond strength (according to AFERA 5001) is carried out as follows. As a defined primer, galvanized steel sheet with a thickness of 2 mm (supplied by Rochöll GmbH) is used. The glued surface element to be examined is cut to a width of 20 mm and a length of about 25 cm, provided with a handling section and immediately thereafter pressed five times with a steel roller of 4 kg at a feed rate of 10 m / min on the selected primer. Immediately thereafter, the glued surface element is removed at an angle of 180 ° from the primer with a tensile testing device (Zwick) at a speed v = 300 mm / min and measured the force required for this at room temperature. The measured value (in N / cm) is the average of three individual measurements.

Melt Index (MFI)

The melt index (MFI) is measured according to ISO 1133. For polyethylenes this is determined at 190 ° C and a weight of 2.16 kg, for polypropylenes at a temperature of 230 ° C and a weight of 2.16 kg.

Bending modulus (bending modulus, flexural modulus)

The test is carried out according to ASTM D 790 A (2% Secant), ie according to "Procedure A" (see, inter alia, Item 1 of the ASTM) with a test specimen to determine the bending modulus with the dimensions 0.125 "x 0.5" x 5.0 "(3.2 mm x 12.7 mm x 125 mm).

crystallite

The crystallite melting point of copolymers, hard and soft blocks and uncured reactive resins is determined by calorimetry using Differential Scanning Calorimetry (DSC) DIN 53765: 1994-03 certainly. Heating curves run at a heating rate of 10 K / min. The samples are measured in Al crucibles with perforated lid and nitrogen atmosphere. The second heating curve is evaluated. In the case of amorphous materials, glass transition temperatures occur; in the case of (semi) crystalline materials, melting temperatures. A glass transition is recognizable as a step in the thermogram. The glass transition temperature is evaluated as the center of this stage. A melting temperature can be recognized as a peak in the thermogram. The melting temperature is the temperature at which the highest heat of reaction occurs.

density

The density is measured according to ASTM D 792.

Molecular Weight Determination

The molecular weight determinations of the weight-average molecular weights Mw were made by gel permeation chromatography (GPC). The eluent used was THF (tetrahydrofuran) containing 0.1% by volume of trifluoroacetic acid. The measurement was carried out at 25 ° C. The precolumn used was PSS-SDV, 5 μ, 10 ³ Å, ID 8.0 mm × 50 mm. For separation, the columns PSS-SDV, 5 μ, 10 ³ and 105 and 106 were used each with ID 8.0 mm × 300 mm. The sample concentration was 4 g / l, the flow rate 1.0 ml per minute. It was measured against PMMA standards.

QUOTES INCLUDE IN THE DESCRIPTION

This list of the documents listed by the applicant has been generated automatically and is included solely for the better information of the reader. The list is not part of the German patent or utility model application. The DPMA assumes no liability for any errors or omissions.

Cited patent literature

• DE 4313008 A1 [0065]
• DE 2845541 A [0092]
• EP 1336683 B1 [0092]

Cited non-patent literature

• Ullmann's "Encyclodedia of Industrial Chemistry", keyword "Polypropylene" by M. Gahleitner and C. Paulik, Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim 2014 [0041]
• Schubnell, M .: "Determination of Crystallinity in Polymers from DSC Measurements"; Mettler Toledo Germany; de.mt.com; USERCOM vol. 1, 2001, pages 12 to 13 [0124]
• DIN 53765: 1994-03 [0129]

Claims (15)

Adhesive tape with a carrier made of a film, to which an adhesive is applied at least on one side, the film being a monoaxially stretched film containing at least 95% by weight, preferably 99% by weight, more preferably 100% by weight. % of propylene polymer composition having different phases, comprising the following components: i) 80 to 99% by weight, preferably 93 to 96% by weight, based on the total weight of components i) and ii) of a propylene polymer matrix containing Propylene homopolymer, and more preferably comprises a preferably random propylene copolymer having a comonomer selected from ethylene or C ₄ to C ₁₀ α-olefins, the propylene polymer matrix having a comonomer content of not more than 15% by weight; ii) 1 to 20 wt .-%, preferably 4 to 7 wt .-%, based on the total weight of components i) and ii), of an elastomer in the form of an ethylene-propylene copolymer having an ethylene content of 50 to 90 wt. -%. Adhesive tape after Claim 1 , characterized in that the propylene polymer composition consists only of components i) and ii). Adhesive tape after Claim 1 or 2 , characterized in that the proportions in component i) of propylene homopolymer and of propylene copolymer are distributed as follows: 70 to 99% by weight of propylene homopolymer and 1 to 30% by weight of propylene copolymer Adhesive tape after at least one of Claims 1 to 3 , characterized in that the propylene polymer matrix has a melt flow index MFI of 0.5 to 10 g / 10 min (measured according to ISO 1133 at 230 ° C and under a weight of 2.16 kg) and an -E modulus of 1000 to 1300 MPa having. Adhesive tape according to at least one of the preceding claims, characterized in that the polypropylene homopolymer is a granule containing as polymer only polypropylene. Adhesive tape according to at least one of the preceding claims, characterized in that selected in the propylene copolymer as the comonomer ethylene with an ethylene-propylene ratio of 0.9: 1 to 1.1: 1. Adhesive tape according to at least one of the preceding claims, characterized in that in the elastomer in the form of an ethylene-propylene copolymer, the ethylene content is 55 to 80 wt .-% is particularly preferably 65 to 75 wt .-%. Adhesive tape according to at least one of the preceding claims, characterized in that the melting point (DSC) of the elastomer is less than 70 ° C. Adhesive tape according to at least one of the preceding claims, characterized in that the degree of crystallinity of component ii) is 0.1. Adhesive tape according to at least one of the preceding claims, characterized in that the stretching ratio in the stretching of the extruded primary film in the longitudinal direction is 1: 5 to 1: 9, preferably 1: 6 to 1: 8. Adhesive tape according to at least one of the preceding claims, characterized in that the film thickness after stretching between 40 and 150 microns, preferably 50 to 100 microns. Adhesive tape according to at least one of the preceding claims, characterized in that the adhesive is selected from the group of natural rubbers or from any blend of natural rubbers and synthetic rubbers. Adhesive tape according to at least one of the preceding claims, characterized in that are used as adhesive resins based on hydrogenated, partially hydrogenated or non-hydrogenated hydrocarbon resins, terpene phenols and rosin esters. Adhesive tape according to at least one of the preceding claims, characterized in that the adhesive contains at least one UV protection agent and / or other admixing components, in particular Plasticizers, anti-aging agents, processing aids, fillers, dyes, optical brighteners, stabilizers, endblocker resins. A film wherein the film is a monoaxially stretched film consisting of at least 95% by weight, preferably 99% by weight, more preferably 100% by weight of propylene polymer composition having different phases, comprising the following components: i 80 to 99% by weight, preferably 93 to 96% by weight, based on the total weight of components i) and ii) of a propylene polymer matrix which comprises a propylene homopolymer and more preferably a preferably random propylene copolymer which comprises a comonomer, selected from ethylene or C ₄ to C ₁₀ α-olefins, the propylene polymer matrix having a comonomer content of not more than 15% by weight; ii) 1 to 20 wt .-%, preferably 4 to 7 wt .-%, based on the total weight of components i) and ii), of an elastomer in the form of an ethylene-propylene copolymer having an ethylene content of 50 to 90 wt. -%.

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