Classifications

• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
  • C08J5/00—Manufacture of articles or shaped materials containing macromolecular substances
  • C08J5/18—Manufacture of films or sheets
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
  • C08J3/00—Processes of treating or compounding macromolecular substances
  • C08J3/28—Treatment by wave energy or particle radiation
• • C—CHEMISTRY; METALLURGY
  • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
  • C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
  • C09J7/00—Adhesives in the form of films or foils
  • C09J7/20—Adhesives in the form of films or foils characterised by their carriers
  • C09J7/22—Plastics; Metallised plastics
  • C09J7/24—Plastics; Metallised plastics based on macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
  • C09J7/241—Polyolefin, e.g.rubber
• • C—CHEMISTRY; METALLURGY
  • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
  • C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
  • C09J7/00—Adhesives in the form of films or foils
  • C09J7/20—Adhesives in the form of films or foils characterised by their carriers
  • C09J7/29—Laminated material
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B05—SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
  • B05B—SPRAYING APPARATUS; ATOMISING APPARATUS; NOZZLES
  • B05B12/00—Arrangements for controlling delivery; Arrangements for controlling the spray area
  • B05B12/16—Arrangements for controlling delivery; Arrangements for controlling the spray area for controlling the spray area
  • B05B12/20—Masking elements, i.e. elements defining uncoated areas on an object to be coated
  • B05B12/24—Masking elements, i.e. elements defining uncoated areas on an object to be coated made at least partly of flexible material, e.g. sheets of paper or fabric
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
  • C08J2323/00—Characterised by the use of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Derivatives of such polymers
  • C08J2323/02—Characterised by the use of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Derivatives of such polymers not modified by chemical after treatment
  • C08J2323/10—Homopolymers or copolymers of propene
• • C—CHEMISTRY; METALLURGY
  • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
  • C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
  • C09J2203/00—Applications of adhesives in processes or use of adhesives in the form of films or foils
  • C09J2203/31—Applications of adhesives in processes or use of adhesives in the form of films or foils as a masking tape for painting
• • C—CHEMISTRY; METALLURGY
  • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
  • C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
  • C09J2301/00—Additional features of adhesives in the form of films or foils
  • C09J2301/10—Additional features of adhesives in the form of films or foils characterized by the structural features of the adhesive tape or sheet
  • C09J2301/16—Additional features of adhesives in the form of films or foils characterized by the structural features of the adhesive tape or sheet by the structure of the carrier layer
  • C09J2301/162—Additional features of adhesives in the form of films or foils characterized by the structural features of the adhesive tape or sheet by the structure of the carrier layer the carrier being a laminate constituted by plastic layers only
• • C—CHEMISTRY; METALLURGY
  • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
  • C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
  • C09J2423/00—Presence of polyolefin
  • C09J2423/006—Presence of polyolefin in the substrate
• • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
  • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
  • Y10T156/00—Adhesive bonding and miscellaneous chemical manufacture
  • Y10T156/10—Methods of surface bonding and/or assembly therefor
• • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
  • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
  • Y10T428/00—Stock material or miscellaneous articles
  • Y10T428/28—Web or sheet containing structurally defined element or component and having an adhesive outermost layer
• • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
  • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
  • Y10T428/00—Stock material or miscellaneous articles
  • Y10T428/28—Web or sheet containing structurally defined element or component and having an adhesive outermost layer
  • Y10T428/2848—Three or more layers

Definitions

• the invention relates to the use of a halogen-free film in a masking tape, wherein the film is electronically pierceable by electron beam irradiation, in particular in a masking tape or in a masking adhesive film (hereinafter the term (masking) adhesive tape also covers (masking) adhesive films) for masking purposes to achieve two-tone designed objects in which at least a portion of the article by masking with the masking tape recessed from painting while a sharp dividing line between painted and unpainted area is achieved.
• the term (masking) adhesive tape also covers (masking) adhesive films) for masking purposes to achieve two-tone designed objects in which at least a portion of the article by masking with the masking tape recessed from painting while a sharp dividing line between painted and unpainted area is achieved.
• the two-color design of vehicles and especially vehicle attachment parts is a frequently used design element.
• a method that has been established for many years for producing the same is masking with masking tapes. Since often plastic parts, in particular plastic bumpers are designed bicoloured, which significantly expand at the drying temperatures of the applied paints of up to 150 ° C, these bands are usually constructed of a soft PVC carrier and a self-adhesive applied on one side. These follow, unlike the otherwise common for painting purposes paper tapes, the thermal expansion, whereas paper in the oven heat due to dehydration even tends to shrink.
• the soft PVC strips commonly used today also conform to curved substrate contours, withstand the usual pretreatments of the plastic parts prior to painting, such as powerful initial cleaning with hot washing solutions ("power wash”) and pretreatment of the cleaned plastic substrate with open flames to improve paint adhesion As already mentioned, they follow easily the sometimes considerable extent of the substrate during the paint drying and can be easily removed after cooling of the substrate without tearing.
• power wash powerful initial cleaning with hot washing solutions
• Framework conditions are burned, on the one hand to reduce the risk of dioxin formation and on the other to purify the flue gas from the hydrogen chloride gas formed.
• Adhesive tapes based on a flexible PVC film are described, for example, in GB 2,171,712 A.
• Conventional soft PVC tapes contain greater than 37 parts by weight of a phthalate based monomer softener per 100 parts by weight of the regularly uncrosslinked PVC polymer. These soft PVC tapes then usually have too high a tensile strength and elongation at break, so that tearing off the masking tape is difficult without technical aids such as scissors or knives.
• the film contains from 2 to 25 parts by weight of an additive polymer, in the form of a crosslinked or PVC-incompatible polymer, per 100 parts by weight of the PVC polymer and from 25 to 37 parts by weight of a polymer plasticizer per 100 parts by weight of the PVC polymer.
• the paint drying temperatures of up to 150 ° C usually require the presence of a polypropylene, as polyethylenes melt at a maximum of 140 ° C and then shrink strongly in the molten state and recrystallization on cooling.
• a polypropylene as polyethylenes melt at a maximum of 140 ° C and then shrink strongly in the molten state and recrystallization on cooling.
• an adhesive tape which has a film carrier.
• the film consists of a mixture of • 100 parts by weight of a polypropylene
• the film is stretched by a factor of 1.05 to 3. In the longitudinal direction.
• a crosslinker is added and the film is then electron beam crosslinked, with a radiation dose of less than 2.5 MGy. In the examples, 1 MGy is irradiated.
• the irradiation serves to improve the temperature resistance of the adhesive tape, as can be seen from the explanations on Examples 3, 4 and 11.
• the object of the present invention is to provide a film which is suitable as a carrier film, for example in a masking tape for two-color, in particular for the coating of plastic attachments, and the known from relevant films disadvantages of the prior art, not or not has the measure.
• a masking tape produced with the film is intended Environmentally friendly, can be used for paint drying temperatures of up to 150 ° C and can easily be tapped by hand.
• the invention relates to the use of a halogen-free film of polyolefins in a one-sided adhesive masking tape, which is preferably used in the two-color finish of plastic attachments, wherein the film of a mixture of a polypropylene or a polypropylene copolymer and another polymer selected from the group the polyethylene or copolymers of ethylene, the film is irradiated with a dose between 5 and 100 kGy (kilogray) before or after coating with the adhesive, and the weight fraction of polypropylene or polypropylene copolymer is at least 20%, based on the total the polyolefins is.
• a halogen-free film of polyolefins in a one-sided adhesive masking tape, which is preferably used in the two-color finish of plastic attachments, wherein the film of a mixture of a polypropylene or a polypropylene copolymer and another polymer selected from the group the polyethylene or copolymers of
• the further polymer is an ethylene-styrene copolymer or a copolymer of ethylene with polar comonomers such as acrylic acid, vinyl acetate or maleic anhydride.
• the proportion by weight of polypropylene or polypropylene copolymer according to an advantageous embodiment of the invention is at least 40% based on the totality of the polyolefins. More preferably, the weight fraction of polypropylene or polypropylene copolymer is at most 90%, particularly preferably at most 80%, very particularly preferably at most 70%, based on the totality of the polyolefins.
• polypropylene component are polypropylene block copolymers.
• the electron beam dose with which the film is irradiated is between 5 and 100 kGy (kilogray), preferably between 10 and 60 kGy.
• the polyolefins other than polypropylene or polypropylene copolymer are, for example, polyethylene or copolymers of ethylene.
• the copolymers of ethylene consist of ethylene and a copolymerizable with ethylene monomer component.
• the film according to the invention consists of polyolefins.
• the film contains polypropylene as homopolymer or polypropylene copolymers, such as random polypropylene copolymers in which a comonomer is randomly distributed throughout the chain.
• polypropylene is used for this purpose.
• Typical random copolymers of polypropylene contain about 2 to 10 mole percent ethylene.
• EPM ethylene propylene copolymers
• these also include copolymers of ethylene, propylene and dienes such as ethylidenenorbornene, dicyclopentadiene or 1,4-cycloocadiene (EPDM).
• Another class of polypropylene copolymers are the block copolymers, also referred to as heterophasic polypropylenes, in which sequences of propylene homopolymer alternate with sequences of random polypropylene-ethylene copolymer.
• the modulus of elasticity of the polypropylene block copolymers is intermediate between those of the propylene homopolymers and the random polypropylene copolymers.
• the polypropylenes are alloyed with other polyolefins.
• Particularly suitable are those from the group of polyethylenes. These include homopolymers of ethylene such as high density polyethylene (LDPE) and low density polyethylene (HDPE), but also the copolymers of ethylene, especially those with ⁇ -olefins such as 1-butene, 1-hexene, 1-octene (depending on the proportion and method of preparation LLDPE But also ethylene-styrene copolymers and copolymers of ethylene with polar comonomers such as acrylic acid, vinyl acetate or maleic anhydride.
• LDPE high density polyethylene
• HDPE low density polyethylene
• ⁇ -olefins such as 1-butene, 1-hexene, 1-octene (depending on the proportion and method of preparation LLDPE
• ethylene-styrene copolymers and copolymers of ethylene with polar comonomers such as acrylic acid,
• Chillroll compiler in which the emerging from a slot die melt is poured onto a chill roll on which the melt solidifies into a film.
• Farther widespread is the blown film process, in which the melt emerges in a tubular form from an annular die and is inflated more or less strongly in order to achieve the desired dimensions (thickness and diameter) of the hose.
• the melt is produced in extruders made of plastic granules.
• An extruder consists of a screw that rotates in a temperature-controlled jacket. At the rear end of the screw, the granulate mixture is drawn in, melted by external heating and conveyed under shear to the end of the extruder, wherein, depending on the configuration of the screw, intensive mixing of the various components is produced.
• a worm consists for this purpose of several zones, for example feeder, compression, metering zone sometimes with shear, decompression and discharge zone, the latter also often with mixing part.
• the screw movement of the melt in the screw generates a pressure in the direction of the front end, which ensures the discharge of the melt into the nozzles described above.
• twin-screw extruders are suitable, in which two screws rotate in the same direction or in opposite directions and thus develop a particularly good mixing effect.
• melt index Melt Flow
• Films of the masking tape according to the invention are polyolefins having an MFR under the above-mentioned conditions of 0.5 to 15 g / 10 min (190 ° C / 2.16 kg for polyethylenes or 230 ° C / 2.16 kg for polypropylenes).
• the film formulation can be extended with additives.
• additives include, for example, fillers such as chalk, talc or titanium dioxide or anti-aging agents, for example based on amines or phenols, also in combination with secondary antioxidants such as phosphites and sulfites.
• HALS sterically hindered amines
• UV absorbers including benzotriazoles and benzophenones
• metal deactivators may be advantageous, including hydrazines and hydrazides. Dyes or colored pigments are to be used for the optical design, also in conjunction with fillers in order to achieve colored transparency, translucence or covering color.
• Lubricants and antiblocking agents such as erucamide, oleamide, glyceryl monostearate, as well as acid scavengers such as calcium stearate and other metal soaps may be used as long as they do not interfere with the adhesive properties of the self-adhesive by migration or stamping from the masking tape back onto the self-adhesive.
• the elongation at break of the film according to the invention is according to an advantageous development more than 100% (pulling speed: 300 mm per minute, temperature: 23 ⁇ 1 ° C, relative humidity: 50 ⁇ 5%) and / or the tensile stress at 1% elongation 1 to 10 N / cm, preferably 1.5 to 6 N / cm.
• the film may be multilayered, either by coextrusion or by hot lamination or laminating with a laminating adhesive.
• a coating of the film with a different type of polymer such as polyamide, polyester or a polyethylene for modifying sliding or optical properties is also included within the scope of the invention.
• the film is unstretched. According to a further advantageous embodiment, no crosslinking agents are added to the film.
• the film is coated on at least one side with an adhesive, preferably self-adhesive.
• an adhesive preferably self-adhesive.
• Suitable self-adhesive compositions are in principle all common pressure-sensitive adhesive systems. These include resin-blended natural rubber self-adhesive compositions,
• Acrylic acid ester copolymers (with and without the addition of tackifier resins), synthetic rubber compositions (for example based on butyl rubber, polyisobutylene, styrene-butadiene copolymers, hydrogenated and non-hydrogenated styrene block copolymers, ethylene-propylene copolymers, amorphous poly- ⁇ -olefins,
• the self-adhesive compositions can be applied to the polyolefin film from solution, from the melt or, if available, as an aqueous dispersion with suitable coating auxiliaries.
• suitable coating auxiliaries are particularly suitable.
• Particularly suitable are very cohesive self-adhesives with peel forces of steel from 1 to 8 N / cm according to AFERA 5001, method A.
• the coating thicknesses of the self-adhesive compositions are preferably 5 to 100 g / m 2 , more preferably 8 to 50 g / m 2 .
• All adhesives may be blended with plasticizers, tackifier resins or other additives such as anti-aging agents and fillers.
• the anchoring of the self-adhesive composition can be improved by coating with a primer as anchoring aid. This can also serve as a corona or a flame pretreatment of the film side to be coated.
• 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,
• the masking tape may be presented as a blank on a release paper or release liner (which are typically silicone-coated papers or plastic films).
• adheresive 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, diecuts and the like.
• the coating of the carrier with primer and / or backside lacquer is carried out by conventional coating methods such as doctor blade or roller application, spraying or casting.
• the self-adhesive composition may also be applied to the carrier in the transfer process, in which the adhesive is coated on a subhesive auxiliary carrier and laminated to the carrier in the dried state.
• the film according to the invention is very well suited as a carrier film in a masking tape, which can be used for two-color painting of plastic attachment parts.
• the known films are generally not easy to tear by hand.
• the requirement for a masking tape for the two-color coating of plastic attachments is an effortless Quereinißißraj by hand, so that the masking process on the one hand proceeds quickly, on the other hand no tool must be used.
• either the film according to the invention before the further coating or else the adhesive tape or cover tape already coated with self-adhesive composition is irradiated with electron beams.
• the film or masking tape is guided past an electron source in a single layer, from which accelerated electrons emerge with a kinetic energy of approximately 10 5 to 10 7 electron volts.
• accelerated electrons For the irradiation of thin films such as foils typically energies up to 300 kiloelectron volts (keV) are applied.
• the generation of the accelerated electrons occurs in electron accelerators, for example scanning accelerators, which operate similarly to a television tube, or in other types, such as linear cathode accelerators or segmented cathode accelerators.
• the absorbed dose of radiation is decisive. Its SI unit is Gray (Gy) or J / g, so it has the dimension of an energy density. Another important quantity is the penetration depth, which is a function of the kinetic energy, ie the acceleration voltage of the electron accelerator.
• the electrons penetrating into the web with the described kinetic energies break chemical bonds to form radicals. These either recombine with other radicals or are eliminated by rearrangement reactions. If the radicals are formed on the main chain of polymers, the reaction kinetics of the recombination reaction in competition with a rearrangement with cleavage of the polymer backbone decides whether it comes to a cross-linking of the polymer or for molecular weight reduction.
• Manual hand tearability can be improved in the sense of the invention at radiation dosages of 5 to 100 kilogray (kGy), the dose to be used being dependent upon the degree of tearability, film formulation and film thickness desired.
• the edge of the crack is more even than when irradiated with electron beams.
• the elongation at break of the support according to the invention is preferably more than 100% (tensile speed: 300 mm per minute, temperature: 23 ⁇ 1 ° C, relative humidity: 50 ⁇ 5%) so that it does not allow for stretching to accommodate curved bonding geometries and peeling Tear off the masking tape comes.
• the tensile stress at 1% elongation is preferably 1 to 10 N / cm, more preferably 1.5 to 6 N / cm, to ensure easy workability in conforming to curves and good conformability to the primer.
• the adhesive tape with the film according to the invention is usually unwound from a roll before use. It can be easily torn off by hand and with a straight crack edge of the required length and applied to the two-color part to be painted along the desired edge of the paint. Alternatively, a stamped product is peeled off from the separating medium (release film or release paper) and placed. The tape snugly adapts to the contours of the component, even through depressions or around curves.
• the masking can be supplemented by large-area adhesive films or non-adhesive sheet materials such as plastic or metal foils or paper. The component can be cleaned together with the mask and prepared for priming or pre-treatment with an open flame for painting.
• the paint system usually multi-layered, is usually sprayed on automatically and freed in drying facilities for up to one hour at up to 150 ° C from the solvent. After cooling, the masking is removed. There is no self-adhesive residue caused by shrinkage and no tearing of the wearer. Lacquer sprayed on the back of the masking tape does not burst during unmasking.
• parts mean parts by weight.
• a film was composed of 60 parts of a polypropylene block copolymer having a MFR of 5.0 g / 10 min (230 ° C, 2.16 kg) and a melting point of about 160 ° C and 40 parts of a low density polyethylene an MFR of 2.0 g / 10 min (190 ° C, 2.16 kg) and a density of 927 kg / m 3 together with 0.4 part of a primary antioxidant (Irganox 1010, Ciba) in a thickness of 90 ⁇ m and a usable width of 40 cm extruded.
• a primary antioxidant Irganox 1010, Ciba
• This film was pretreated unilaterally on a pilot plant with a corona discharge to a surface energy of 48 mN / im and then coated with the solution of an acrylic acid ester copolymer as a self-adhesive in such a way that a mass application of 25 g / m 2 resulted.
• the self-adhesive was a polymer of 40 parts of butyl acrylate, 40 parts of 2-ethylhexyl acrylate, 12 parts of vinyl acetate, 4.5 parts of methyl acrylate, 3 parts of acrylic acid and 0.5 parts of aluminum acetylacetonate.
• the film was irradiated in an ESH facility under a nitrogen atmosphere with an accelerating voltage of 200 kV and a dose of 35 kGy, and then wound into a full-width roll.
• Example 4 As in Example 2, except that the coated film was irradiated with an ESH dose of 80 kGy.
• Example 4 As in Example 2, except that the coated film was irradiated with an ESH dose of 80 kGy.
• Example 1 As for Example 1, except for the film, 50 parts of a polypropylene block copolymer having an MFR of 5.0 g / 10 min (230 ° C, 2.16 kg) and a melting point of about 160 ° C, 25 parts of a Low Density Polyethylene with a
• Linear low density polyethylene with 1-butene as comonomer with a MFR of 1, 2 g / 10 min (190 ° C, 2.16 kg) and a density of 919 kg / m 3 and 5 parts of talc used.
• Example 1 As in Example 1 except that the 60 parts polypropylene block copolymer was replaced with 40 parts polypropylene homopolymer having MFR of 8.0 g / 10 min (230 ° C, 2.16 kg) and a melting point of about 164 ° C and 20 parts polypropylene random copolymer with a MFR of 1.9 g / 10 min (230 ° C, 2.16 kg) and a melting point of about 145 ° C replaced.
• Example 1 in contrast to this, the film was driven through the ESH system before the coating with adhesive and irradiated with electrons.
• Example 2 As in Example 1 except that the film was composed of 40 parts of a low density polyethylene having an MFR of 2.0 g / 10 min (190 ° C, 2.16 kg) and a density of 927 kg / m 3 and 60 Dividing a linear low density polyethylene with 1-butene as a comonomer with a MFR of 1, 2 g / 10 min (190 ° C, 2.16 kg) and a density of 919 kg / m 3 together.
• MFR 2.0 g / 10 min
• 927 kg / m 3 60
• 6 Dividing a linear low density polyethylene with 1-butene as a comonomer with a MFR of 1, 2 g / 10 min (190 ° C, 2.16 kg) and a density of 919 kg / m 3 together.
• Example 1 As in Example 1 except that the film consisted of 40 parts of a polypropylene homopolymer having an MFR of 8.0 g / 10 min (230 ° C, 2.16 kg) and a melting point of about 164 ° C and 60 parts of polypropylene random copolymer an MFR of 1.9 g / 10 min (230 ° C, 2.16 kg) and a melting point of about 145 ° C
• Example 2 As in Example 1, by contrast, the coated film was not irradiated with ESH radiation.
• Example 6 As in Example 6 except that the ESH irradiation was omitted.
• Example 2 As in Example 1, in contrast to this was irradiated with 130 kGy ESH dose.
• Strips of sample samples 15 mm wide and 15 cm long (in the machine direction) were bonded to an aluminum sheet and pressed with a pressure roller as described in the AFERA Method 5001. With a cutter, the strips were cut in the middle perpendicular to the longitudinal direction down to the aluminum sheet base. This was followed by a heat load of one hour at 150 ° C in a warming cabinet. The shrinkage in the form of the widening of the gap was evaluated at the incision as follows:
• the bands of the examples demonstrate compliance with the essential test criteria relevant to a masking tape for two-color painting.
• These exemplary masking tapes have an application-grade peel force from a typical plastic substrate, can be used during application to the

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• Chemical & Material Sciences (AREA)
• Organic Chemistry (AREA)
• Chemical Kinetics & Catalysis (AREA)
• Health & Medical Sciences (AREA)
• Medicinal Chemistry (AREA)
• Polymers & Plastics (AREA)
• Engineering & Computer Science (AREA)
• Manufacturing & Machinery (AREA)
• Materials Engineering (AREA)
• Adhesive Tapes (AREA)
• Laminated Bodies (AREA)
• Treatments Of Macromolecular Shaped Articles (AREA)

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• 2006
  • 2006-05-18 DE DE102006023743A patent/DE102006023743A1/de not_active Withdrawn
• 2007
  • 2007-05-16 AT AT07729197T patent/ATE482260T1/de active
  • 2007-05-16 WO PCT/EP2007/054749 patent/WO2007135050A1/de not_active Ceased
  • 2007-05-16 EP EP07729197A patent/EP2024456B1/de not_active Revoked
  • 2007-05-16 US US12/300,728 patent/US20090277577A1/en not_active Abandoned
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