EP0710266A1 - Pressure sensitive adhesive film - Google Patents

Pressure sensitive adhesive film

Info

Publication number
EP0710266A1
EP0710266A1 EP94921659A EP94921659A EP0710266A1 EP 0710266 A1 EP0710266 A1 EP 0710266A1 EP 94921659 A EP94921659 A EP 94921659A EP 94921659 A EP94921659 A EP 94921659A EP 0710266 A1 EP0710266 A1 EP 0710266A1
Authority
EP
European Patent Office
Prior art keywords
film structure
structure according
support
hdpe
layer
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
EP94921659A
Other languages
German (de)
French (fr)
Inventor
Benoit Ambroise
Maurice Petitjean
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Jindal Films Europe Virton SPRL
Original Assignee
Mobil Plastics Europe Inc Belgium
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Mobil Plastics Europe Inc Belgium filed Critical Mobil Plastics Europe Inc Belgium
Publication of EP0710266A1 publication Critical patent/EP0710266A1/en
Withdrawn legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J7/00Adhesives in the form of films or foils
    • C09J7/20Adhesives in the form of films or foils characterised by their carriers
    • C09J7/29Laminated material
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B27/00Layered products comprising a layer of synthetic resin
    • B32B27/06Layered products comprising a layer of synthetic resin as the main or only constituent of a layer, which is next to another layer of the same or of a different material
    • B32B27/08Layered products comprising a layer of synthetic resin as the main or only constituent of a layer, which is next to another layer of the same or of a different material of synthetic resin
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B27/00Layered products comprising a layer of synthetic resin
    • B32B27/32Layered products comprising a layer of synthetic resin comprising polyolefins
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B7/00Layered products characterised by the relation between layers; Layered products characterised by the relative orientation of features between layers, or by the relative values of a measurable parameter between layers, i.e. products comprising layers having different physical, chemical or physicochemical properties; Layered products characterised by the interconnection of layers
    • B32B7/04Interconnection of layers
    • B32B7/12Interconnection of layers using interposed adhesives or interposed materials with bonding properties
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2307/00Properties of the layers or laminate
    • B32B2307/50Properties of the layers or laminate having particular mechanical properties
    • B32B2307/514Oriented
    • B32B2307/518Oriented bi-axially
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2323/00Polyalkenes
    • B32B2323/04Polyethylene
    • B32B2323/043HDPE, i.e. high density polyethylene
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J2301/00Additional features of adhesives in the form of films or foils
    • C09J2301/10Additional features of adhesives in the form of films or foils characterized by the structural features of the adhesive tape or sheet
    • C09J2301/16Additional 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
    • C09J2301/162Additional 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

Definitions

  • This invention relates to an adhesive film; more particularly, this invention relates to a pressure sensitive adhesive film, preferably in tape form.
  • Adhesive films generally comprise a support provided on one surface with a pressure sensitive adhesive coating, and provided on the other surface with a release coating.
  • the purpose of the release coating is to prevent the film from sticking too strongly to itself when it has been wound on a roll, so that it can be readily unwound from the roll. Without a release coating it can be difficult or impossible to unwind the film from the roll; and during unwinding the adhesive tends to transfer from one surface of the film to the other. Finally, the unwinding process in films of the prior art can be quite noisy.
  • US 4673611 discloses an adhesive tape which can be drawn from a roll which comprises a coextruded, biaxially oriented, multilayer polypropylene support film and an adhesive layer.
  • the support comprises at least two polypropylene layers having different compositions; the second layer of the support, which faces away from the adhesive coating, has a thickness of less than one third of the total thickness of the adhesive tape and contains an anti-adhesive substance (for example from 0.2 wt% to about 3.0% wt% of a polydiorganosiloxane) .
  • This structure has the advantage that a release coating is not needed on the support.
  • the additive is transferred to the adhesive, when the film is wound on a roll, and this causes loss of tackiness in the adhesive.
  • thermoplastic polymeric film structure comprising a support which is coated with a pressure sensitive adhesive on a first surface thereof, wherein a second surface of the support, opposite to the first surface, comprises high density polyethylene (HDPE) .
  • HDPE high density polyethylene
  • CONFIRMATIONCOPT excellent release properties, so that after the film has been wound on a roll it can readily be unwound again without any significant tranfer of adhesive onto the second surface of the support. In addition, it has been found that during unwinding there is less noise than with the pressure sensitive tapes of the prior art.
  • the support may comprise a single layer or a plurality of layers.
  • the HDPE should desirably have a density from 0.930 to 0.965, preferably from 0.945 to 0.955, most preferably 0.950.
  • the support comprises a single layer of HDPE.
  • the second surface of the support has not been subjected to any form of surface treatment.
  • the first surface of the support has been subjected to surface treatment.
  • the support preferably contains from 50 to 100 wt% HDPE, more preferably from 80 to 100 wt% HDPE.
  • the support contains less than 100 wt% HDPE it is preferred that it comprises a blend of HDPE with at least one other olefin polymer.
  • the other olefin polymer may be, for example: a polyethylene of lower density such as linear low density polyethylene (LLDPE) ; low density (high pressure) polyethylene (LDPE) ; medium density polyethylene (MDPE) ; or a copolymer or terpolymer of propylene.
  • the copolymer or terpolymer of propylene is suitably a random or block copolymer of ethylene and propylene or of butylene and propylene; or a random or block terpolymer of ethylene, propylene and butene-1.
  • the preferred copolymers of ethylene and propylene contain from 1 to 30 wt%, preferably from 2 to 7 wt%, more preferably 3 to 5 wt%, ethylene. Also, the preferred copolymers have a melt flow rate at 230°C from 2 to 15, more preferably 3 to 8; a crystalline melting point from 125 to 150°C; a number average molecular weight from 25000 to 100000; and a density from 0.89 to 0.90.
  • the preferred copolymers of butylene and propylene contain up to 30 wt% butylene.
  • the preferred terpolymers of propylene contain from 1 to 10, preferably from 2 to 6, wt% ethylene, from 80 to 97, preferably from 88 to 95, wt% propylene, and from 1 to 20, preferably from 2 to 15, wt% butene-1.
  • the support contains an anti-blocking agent, or other additives.
  • additives are not essential - HDPE has very good release properties without them - but certain additives can produce further improvements to the release properties, and to other desirable properties. Particularly good results have been obtained with silicone oil, EBS (ethylene bis stearamide) , GMS (glycero mono stearate) and montan wax.
  • a preferred silicone oil is a polydialkyl-siloxane.
  • the support has three layers in a structure comprising a core layer, sandwiched between two other layers.
  • a first of said other layers is provided with the adhesive coating on the external surface thereof.
  • a second of said other layers comprises HDPE; the external surface of the second layer faces away from the adhesive coating.
  • the external surface of the second layer has not been subjected to any form of surface treatment.
  • the external surface of the first layer has been subjected to surface treatment prior to the application of the adhesive.
  • the second layer preferably contains from 50 to 100 wt% HDPE, more preferably from 80 to 100 wt% HDPE.
  • the second layer contains less than 100 wt% HDPE it is preferred that it comprises a blend of HDPE with at least one other olefin polymer.
  • the other olefin polymer may be, for example: a polyethylene of lower density such as linear low density polyethylene (LLDPE) ; low density (high pressure) polyethylene (LDPE) ; medium density polyethylene (MDPE) ; or a copolymer or terpolymer of propylene.
  • the copolymer or terpolymer of propylene is suitably a random or block copolymer of ethylene and propylene or of butylene and propylene; or a random or block terpolymer of ethylene, propylene and butene-1.
  • the preferred copolymers of ethylene and propylene contain from 1 to 30 wt%, preferably from 2 to 7 wt%, more preferably 3 to 5 wt%, ethylene. Also, the preferred copolymers have a melt flow rate at 230°C from 2 to 15, more preferably 3 to 8; a crystalline melting point from 125 to 150°C; a number average molecular weight from 25000 to 100000; and a density from 0.89 to 0.90.
  • the preferred copolymers of butylene and propylene contain up to 30 wt% butylene.
  • the preferred terpolymers of propylene contain from 1 to 10, preferably from 2 to 6, wt% ethylene, from 80 to 97, preferably from 88 to 95, wt% propylene, and from 1 to 20, preferably from 2 to 15, wt% butene-1.
  • the second layer contains an anti-blocking agent, or other additives.
  • an anti-blocking agent or other additives.
  • such additives are not essential. Particularly good results have been obtained with silicone oil, EBS, GMS and ontan wax.
  • a preferred silicone oil is a polydialkylsiloxane.
  • the core layer comprises an oriented olefin polymer.
  • the core layer desirably comprises a polymer of propylene, suitably homopolymeric polypropylene and preferably isotactic polypropylene.
  • the core layer may be provided with voids: more specifically, the core layer may be cavitated, for example, as disclosed in EP-A-0083495.
  • a preferred cavitating agent is polybutylene terephthalate, especially as spherical particles.
  • the first layer may comprise any olefin polymer useful in the manufacture of an adhesive liner, or a mixture thereof, and is suitably a polymer of propylene, such as polypropylene.
  • the first layer may comprise any of the materials described above with reference to the second layer. If desired, the first layer may be the same material as the second layer.
  • the first layer comprises HDPE, the external surface of which has been treated to alter its surface properties.
  • the surface treatments discussed above may be achieved, for example, by subjecting the surface to corona discharge, to a flame or to oxidising chemicals; a flame treatment is preferred.
  • the surface is treated to a surface activity of at least 36 dynes/cm (36 mN/m) , more preferably to at least 40 dynes/cm (40 mN/m) .
  • the core layer is preferably coextruded or extrusion coated with the first and second layers, and then the whole support is desirably biaxially oriented.
  • the polymers can be brought to the molten state and coextruded from a conventional extruder through a flat sheet die, the melt streams being combined in an adapter prior to being extruded from the die.
  • the thermoplastic polymeric film structure is chilled and the quenched sheet is then preferably reheated and oriented by stretching (for example, from 4 to 6 times in the machine direction at about 253°F (123°C) and, subsequently, from 8 to 10 times in the transverse direction, at about 310°F (154°C)).
  • thermoplastic polymeric film structure which comprises:
  • the support may comprise a single layer or a plurality of layers.
  • the HDPE should desirably have a density from 0.930 to 0.965, preferably from 0.945 to 0.955, most preferably 0.950.
  • the anti-adhesive material may be any anti-adhesive material known from the prior art, which is coated upon the second surface of the support. Alternatively the anti-adhesive material may be incorporated into the second surface of the support.
  • the anti-adhesive material comprises HDPE, incorporated into the second surface of the support.
  • the support comprises a single layer of HDPE.
  • the second surface of the support has not been subjected to any form of surface treatment.
  • the support preferably contains from 50 to 100 wt% HDPE, more preferably from 80 to 100 wt% HDPE.
  • the support contains less than 100 wt% HDPE it is preferred that it comprises a blend of HDPE with at least one other olefin polymer.
  • the other olefin polymer may be, for example: a polyethylene of lower density such as linear low density polyethylene (LLDPE) ; low density (high pressure) polyethylene (LDPE) ; medium density polyethylene (MDPE) ; or a copolymer or terpolymer of propylene.
  • the copolymer or terpolymer of propylene is suitably a random or block copolymer of ethylene and propylene or of butylene and propylene; or a random or block terpolymer of ethylene, propylene and butene-1.
  • the preferred copolymers of ethylene and propylene contain from 1 to 30 wt%, preferably from 2 to 7 wt%, more preferably 3 to 5 wt%, ethylene. Also, the preferred copolymers have a melt flow rate at 230°C from 2 to 15, more preferably 3 to 8; a crystalline melting point from 125 to 150°C; a number average molecular weight from 25000 to 100000; and a density from 0.89 to 0.90.
  • the preferred copolymers of butylene and propylene contain up to 30 wt% butylene.
  • the preferred terpolymers of propylene contain from 1 to 10, preferably from 2 to 6, wt% ethylene, from 80 to 97, preferably from 88 to 95, wt% propylene, and from 1 to 20, preferably from 2 to 15, wt% butene-1.
  • the support contains an anti-blocking agent, or other additives.
  • additives are not essential - HDPE has very good release properties without them - but certain additives can produce further improvements to the release properties, and to other desirable properties. Particularly good results have been obtained with silicone oil, EBS, GMS and ontan wax.
  • a preferred silicone oil is a polydialkyl-siloxane.
  • the support has three layers in a structure comprising a core layer, sandwiched between two other layers.
  • a first of said other layers is provided with the adhesive coating on the external surface thereof.
  • a second of said other layers comprises HDPE; the external surface of the second layer faces away from the adhesive coating.
  • the external surface of the second layer has not been subjected to any form of surface treatment.
  • the second layer preferably contains from 50 to 100 wt% HDPE, more preferably from 80 to 100 wt% HDPE.
  • the second layer contains less than 100 wt% HDPE it is preferred that it comprises a blend of HDPE with at least one other olefin polymer.
  • the other olefin polymer may be, for example: a polyethylene of lower density such as linear low density polyethylene (LLDPE) ; low density (high pressure) polyethylene (LDPE) ; medium density polyethylene (MDPE) ; or a copolymer or terpolymer of propylene.
  • the copolymer or terpolymer of propylene is suitably a random or block copolymer of ethylene and propylene or of butylene and propylene; or a random or block terpolymer of ethylene, propylene and butene-1.
  • the preferred copolymers of ethylene and propylene contain from 1 to 30 wt%, preferably from 2 to 7 wt%, more preferably 3 to 5 wt%, ethylene. Also, the preferred copolymers have a melt flow rate at 230°C from 2 to 15, more preferably 3 to 8; a crystalline melting point from 125 to 150°C; a number average molecular weight from 25000 to 100000; and a density from 0.89 to 0.90.
  • the preferred copolymers of butylene and propylene contain up to 30 wt% butylene.
  • the preferred terpolymers of propylene contain from 1 to 10, preferably from 2 to 6, wt% ethylene, from 80 to 97, preferably from 88 to 95, wt% propylene, and from 1. to 20, preferably from 2 to 15, wt% butene-1.
  • the second layer contains an anti-blocking agent, or other additives.
  • an anti-blocking agent or other additives.
  • such additives are not essential. Particularly good results have been obtained with silicone oil, EBS, GMS and montan wax.
  • a preferred silicone oil is a polydialkylsiloxane.
  • the core layer comprises an oriented olefin polymer.
  • the core layer desirably comprises a polymer of propylene, suitably homopolymeric polypropylene and preferably isotactic polypropylene.
  • the core layer may be provided with voids: more specifically, the core layer may be cavitated, for example, as disclosed in EP-A-0083495.
  • a preferred cavitating agent is polybutylene terephthalate, especially as spherical particles.
  • the first layer comprises HDPE which has been treated to alter its surface properties.
  • the first layer may comprise any of the materials described above with reference to the second layer. If desired, the first layer may be the same material as the second layer.
  • the surface treatments discussed above, with reference to the second aspect of the invention may be achieved, for example, by subjecting the surface to corona discharge, to a flame or to oxidising chemicals; a flame treatment is preferred.
  • the surface is treated to a surface activity of at least 36 dynes/cm (36 mN/m) , more preferably to at least 40 dynes/cm (40 mN/m) .
  • the core layer is preferably coextruded or extrusion coated with the first and second layers, and then the whole support is desirably biaxially oriented.
  • the polymers can be brought to the molten state and coextruded from a conventional extruder through a flat sheet die, the melt streams being combined in an adapter prior to being extruded from the die.
  • the thermoplastic polymeric film structure is chilled and the quenched sheet is then preferably reheated and oriented by stretching; for example, from 4 to 6 times in the machine direction at about 253°F (123°C) and, subsequently,, from 8 to 10 times in the transverse direction, at about 310°F (154°C) .
  • the pressure sensitive adhesive referred to above may be a hot melt adhesive, a solvent based adhesive or a water based adhesive.
  • the invention may be used with any pressure sensitive adhesive used in the adhesive tapes of the prior art.
  • Particular adhesives that may be used include rubber and acrylic based adhesives, which are described in detail in the prior art.
  • Polypropylene homopolymer was fed into the feed hopper of a rotating screw extruder having a 2.5 inch (6.4 cm) diameter and an L:D ratio of 24:1.
  • HDPE density 0.952
  • the molten polyethylene was fed into the slot die fixed to the first extruder through an adaptor designed to ensure that the molten polyethylene stream covered both sides of the molten polypropylene stream.
  • the multi-layer structure was then quenched onto a chill roll to form a cast film which was immediately quenched in a cold water bath and sequentially biaxially oriented on conventional equipment.
  • the quenched film was first reheated to about 253°F (123°C) and stretched 5 times the machine direction between differential speed rollers, and was then fed to a transverse orientor where it was heated to about 310°F (154°C) and stretched 8 times.
  • the film comprising 0.6 ⁇ m HDPE skin, on both sides, was next cooled; and trimmed. Thereafter it was flame treated to > 48 dynes/cm on one side; and wound on a roll. Finally the film was tested, using the following procedure, to demonstrate release effect.
  • PROCEDURE
  • a standard adhesive tape, containing a pressure sensitive adhesive was applied to the treated, or the untreated, side of the prepared film in the MD direction. This provides an adhesive coating on the prepared film, and gives the film a structure in accordance with the invention.
  • the samples were, or were not, stored 24 hours at 50°C.
  • the peel force necessary to separate both the standard tape and the test film was measured at 300 mm/min with the film test and adhesive at 90° angle.
  • Example 2 A film A was prepared using HDPE as the first layer; polypropylene as the core; and HDPE as the second layer. This film was produced by the same method as the film of example 1.
  • Example 3 A film B was prepared by the same method as in Example 1, but the second layer incorporated 12000 ppm of silicone oil.
  • a film C was prepared by the same method as in Example 1, but the second layer incorporated 2000 ppm EBS.
  • Example 5 A film D was prepared by the same method as in Example 1, but the second layer incorporated 2000 ppm GMS.
  • a film E was prepared by the same method as in Example 1, but the second layer incorporated 2000 ppm montan wax.
  • the Films A to E were tested using a similar procedure to example 1: a standard adhesive tape was applied uniformly to the untreated side of each film A to E, and the release force was measured on the untreated side at 300 mm/min and with the test tape at 90°, 135° and 180° angles. The percentage transfer of adhesive when peeling the samples was also observed.
  • the following films were also tested : Film F - Reference tape 35 ⁇ m Film G - PP terpolymer

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Adhesive Tapes (AREA)
  • Laminated Bodies (AREA)

Abstract

A thermoplastic polymeric film structure comprises a support which is coated with a pressure sensitive adhesive on a first surface thereof. A second surface of the support, opposite to the first surface, comprises high density polyethylene (HDPE).

Description

Pressure sensitive adhesive f lm
This invention relates to an adhesive film; more particularly, this invention relates to a pressure sensitive adhesive film, preferably in tape form.
Adhesive films generally comprise a support provided on one surface with a pressure sensitive adhesive coating, and provided on the other surface with a release coating. The purpose of the release coating is to prevent the film from sticking too strongly to itself when it has been wound on a roll, so that it can be readily unwound from the roll. Without a release coating it can be difficult or impossible to unwind the film from the roll; and during unwinding the adhesive tends to transfer from one surface of the film to the other. Finally, the unwinding process in films of the prior art can be quite noisy.
US 4673611 discloses an adhesive tape which can be drawn from a roll which comprises a coextruded, biaxially oriented, multilayer polypropylene support film and an adhesive layer. The support comprises at least two polypropylene layers having different compositions; the second layer of the support, which faces away from the adhesive coating, has a thickness of less than one third of the total thickness of the adhesive tape and contains an anti-adhesive substance (for example from 0.2 wt% to about 3.0% wt% of a polydiorganosiloxane) . This structure has the advantage that a release coating is not needed on the support. However, it is necessary to incorporate an additive into the support. Moreover, the additive is transferred to the adhesive, when the film is wound on a roll, and this causes loss of tackiness in the adhesive.
According to a first aspect of the present invention, there is provided a thermoplastic polymeric film structure comprising a support which is coated with a pressure sensitive adhesive on a first surface thereof, wherein a second surface of the support, opposite to the first surface, comprises high density polyethylene (HDPE) .
It has been found that the presence of HDPE in the surface of the support opposite from the adhesive gives the surface
CONFIRMATIONCOPT excellent release properties, so that after the film has been wound on a roll it can readily be unwound again without any significant tranfer of adhesive onto the second surface of the support. In addition, it has been found that during unwinding there is less noise than with the pressure sensitive tapes of the prior art.
The support may comprise a single layer or a plurality of layers.
The HDPE should desirably have a density from 0.930 to 0.965, preferably from 0.945 to 0.955, most preferably 0.950.
In a first preferred embodiment the support comprises a single layer of HDPE.
Advantageously the second surface of the support has not been subjected to any form of surface treatment. However, it is preferred that the first surface of the support has been subjected to surface treatment.
In the first embodiment the support preferably contains from 50 to 100 wt% HDPE, more preferably from 80 to 100 wt% HDPE. When the support contains less than 100 wt% HDPE it is preferred that it comprises a blend of HDPE with at least one other olefin polymer. The other olefin polymer may be, for example: a polyethylene of lower density such as linear low density polyethylene (LLDPE) ; low density (high pressure) polyethylene (LDPE) ; medium density polyethylene (MDPE) ; or a copolymer or terpolymer of propylene.
The copolymer or terpolymer of propylene is suitably a random or block copolymer of ethylene and propylene or of butylene and propylene; or a random or block terpolymer of ethylene, propylene and butene-1.
The preferred copolymers of ethylene and propylene contain from 1 to 30 wt%, preferably from 2 to 7 wt%, more preferably 3 to 5 wt%, ethylene. Also, the preferred copolymers have a melt flow rate at 230°C from 2 to 15, more preferably 3 to 8; a crystalline melting point from 125 to 150°C; a number average molecular weight from 25000 to 100000; and a density from 0.89 to 0.90.
The preferred copolymers of butylene and propylene contain up to 30 wt% butylene.
The preferred terpolymers of propylene contain from 1 to 10, preferably from 2 to 6, wt% ethylene, from 80 to 97, preferably from 88 to 95, wt% propylene, and from 1 to 20, preferably from 2 to 15, wt% butene-1.
Preferably, the support contains an anti-blocking agent, or other additives. Such additives are not essential - HDPE has very good release properties without them - but certain additives can produce further improvements to the release properties, and to other desirable properties. Particularly good results have been obtained with silicone oil, EBS (ethylene bis stearamide) , GMS (glycero mono stearate) and montan wax. A preferred silicone oil is a polydialkyl-siloxane.
When silicone oil is used there is some transfer of the silicone oil to the surface of the adhesive after the film has been wound onto a roll. However, despite this transfer, good adhesion by the pressure sensitive adhesive coated surface was manifest.
In a second preferred embodiment the support has three layers in a structure comprising a core layer, sandwiched between two other layers. A first of said other layers is provided with the adhesive coating on the external surface thereof. A second of said other layers comprises HDPE; the external surface of the second layer faces away from the adhesive coating.
Advantageously the external surface of the second layer has not been subjected to any form of surface treatment. However, it is preferred that the external surface of the first layer has been subjected to surface treatment prior to the application of the adhesive.
In the second embodiment the second layer preferably contains from 50 to 100 wt% HDPE, more preferably from 80 to 100 wt% HDPE. When the second layer contains less than 100 wt% HDPE it is preferred that it comprises a blend of HDPE with at least one other olefin polymer. The other olefin polymer may be, for example: a polyethylene of lower density such as linear low density polyethylene (LLDPE) ; low density (high pressure) polyethylene (LDPE) ; medium density polyethylene (MDPE) ; or a copolymer or terpolymer of propylene.
The copolymer or terpolymer of propylene is suitably a random or block copolymer of ethylene and propylene or of butylene and propylene; or a random or block terpolymer of ethylene, propylene and butene-1.
The preferred copolymers of ethylene and propylene contain from 1 to 30 wt%, preferably from 2 to 7 wt%, more preferably 3 to 5 wt%, ethylene. Also, the preferred copolymers have a melt flow rate at 230°C from 2 to 15, more preferably 3 to 8; a crystalline melting point from 125 to 150°C; a number average molecular weight from 25000 to 100000; and a density from 0.89 to 0.90.
The preferred copolymers of butylene and propylene contain up to 30 wt% butylene.
The preferred terpolymers of propylene contain from 1 to 10, preferably from 2 to 6, wt% ethylene, from 80 to 97, preferably from 88 to 95, wt% propylene, and from 1 to 20, preferably from 2 to 15, wt% butene-1.
Preferably, the second layer contains an anti-blocking agent, or other additives. As noted above, such additives are not essential. Particularly good results have been obtained with silicone oil, EBS, GMS and ontan wax. A preferred silicone oil is a polydialkylsiloxane.
When silicone oil is used there is some transfer of the silicone oil to the surface of the adhesive after the film has been wound onto a roll. However, despite this transfer, good adhesion by the pressure sensitive adhesive coated surface was manifest.
Preferably the core layer comprises an oriented olefin polymer. The core layer desirably comprises a polymer of propylene, suitably homopolymeric polypropylene and preferably isotactic polypropylene.
The core layer may be provided with voids: more specifically, the core layer may be cavitated, for example, as disclosed in EP-A-0083495. A preferred cavitating agent is polybutylene terephthalate, especially as spherical particles. The first layer may comprise any olefin polymer useful in the manufacture of an adhesive liner, or a mixture thereof, and is suitably a polymer of propylene, such as polypropylene. The first layer may comprise any of the materials described above with reference to the second layer. If desired, the first layer may be the same material as the second layer.
In a particularly advantageous construction the first layer comprises HDPE, the external surface of which has been treated to alter its surface properties.
The surface treatments discussed above may be achieved, for example, by subjecting the surface to corona discharge, to a flame or to oxidising chemicals; a flame treatment is preferred. Preferably, the surface is treated to a surface activity of at least 36 dynes/cm (36 mN/m) , more preferably to at least 40 dynes/cm (40 mN/m) .
In the second embodiment the core layer is preferably coextruded or extrusion coated with the first and second layers, and then the whole support is desirably biaxially oriented. The polymers can be brought to the molten state and coextruded from a conventional extruder through a flat sheet die, the melt streams being combined in an adapter prior to being extruded from the die. After leaving the die orifice, the thermoplastic polymeric film structure is chilled and the quenched sheet is then preferably reheated and oriented by stretching (for example, from 4 to 6 times in the machine direction at about 253°F (123°C) and, subsequently, from 8 to 10 times in the transverse direction, at about 310°F (154°C)).
According to a second aspect of the present invention there is provided a thermoplastic polymeric film structure which comprises:
(a) a support which is coated with a pressure sensitive adhesive on a first surface thereof, said surface comprising HDPE and having been surface treated prior to the application of said adhesive; and
(b) an anti-adhesive material incorporated in or coated on a second surface of the support opposite to the adhesive coating. This aspect of the invention is predicated on the unexpected discovery that adhesive provided on surface treated HDPE has remarkably good adhesive properties. These adhesive properties are most remarkable when the adhesive is a hot melt adhesive. However, good results can be obtained with other adhesives, including solvent based adhesives.
The support may comprise a single layer or a plurality of layers.
The HDPE should desirably have a density from 0.930 to 0.965, preferably from 0.945 to 0.955, most preferably 0.950.
The anti-adhesive material may be any anti-adhesive material known from the prior art, which is coated upon the second surface of the support. Alternatively the anti-adhesive material may be incorporated into the second surface of the support.
It is preferred that the anti-adhesive material comprises HDPE, incorporated into the second surface of the support.
In a first preferred embodiment of the second aspect of the invention the support comprises a single layer of HDPE.
Advantageously the second surface of the support has not been subjected to any form of surface treatment.
In the first embodiment the support preferably contains from 50 to 100 wt% HDPE, more preferably from 80 to 100 wt% HDPE. When the support contains less than 100 wt% HDPE it is preferred that it comprises a blend of HDPE with at least one other olefin polymer. The other olefin polymer may be, for example: a polyethylene of lower density such as linear low density polyethylene (LLDPE) ; low density (high pressure) polyethylene (LDPE) ; medium density polyethylene (MDPE) ; or a copolymer or terpolymer of propylene.
The copolymer or terpolymer of propylene is suitably a random or block copolymer of ethylene and propylene or of butylene and propylene; or a random or block terpolymer of ethylene, propylene and butene-1.
The preferred copolymers of ethylene and propylene contain from 1 to 30 wt%, preferably from 2 to 7 wt%, more preferably 3 to 5 wt%, ethylene. Also, the preferred copolymers have a melt flow rate at 230°C from 2 to 15, more preferably 3 to 8; a crystalline melting point from 125 to 150°C; a number average molecular weight from 25000 to 100000; and a density from 0.89 to 0.90.
The preferred copolymers of butylene and propylene contain up to 30 wt% butylene.
The preferred terpolymers of propylene contain from 1 to 10, preferably from 2 to 6, wt% ethylene, from 80 to 97, preferably from 88 to 95, wt% propylene, and from 1 to 20, preferably from 2 to 15, wt% butene-1.
Preferably, the support contains an anti-blocking agent, or other additives. Such additives are not essential - HDPE has very good release properties without them - but certain additives can produce further improvements to the release properties, and to other desirable properties. Particularly good results have been obtained with silicone oil, EBS, GMS and ontan wax. A preferred silicone oil is a polydialkyl-siloxane.
When silicone oil is used there is some transfer of the silicone oil to the surface of the adhesive after the film has been wound onto a roll. However, despite this transfer good adhesion by the pressure sensitive adhesive coated surface was manifest.
In a second preferred embodiment of the second aspect of the invention the support has three layers in a structure comprising a core layer, sandwiched between two other layers. A first of said other layers is provided with the adhesive coating on the external surface thereof. A second of said other layers comprises HDPE; the external surface of the second layer faces away from the adhesive coating.
Advantageously the external surface of the second layer has not been subjected to any form of surface treatment.
In the second embodiment the second layer preferably contains from 50 to 100 wt% HDPE, more preferably from 80 to 100 wt% HDPE. When the second layer contains less than 100 wt% HDPE it is preferred that it comprises a blend of HDPE with at least one other olefin polymer. The other olefin polymer may be, for example: a polyethylene of lower density such as linear low density polyethylene (LLDPE) ; low density (high pressure) polyethylene (LDPE) ; medium density polyethylene (MDPE) ; or a copolymer or terpolymer of propylene.
The copolymer or terpolymer of propylene is suitably a random or block copolymer of ethylene and propylene or of butylene and propylene; or a random or block terpolymer of ethylene, propylene and butene-1.
The preferred copolymers of ethylene and propylene contain from 1 to 30 wt%, preferably from 2 to 7 wt%, more preferably 3 to 5 wt%, ethylene. Also, the preferred copolymers have a melt flow rate at 230°C from 2 to 15, more preferably 3 to 8; a crystalline melting point from 125 to 150°C; a number average molecular weight from 25000 to 100000; and a density from 0.89 to 0.90.
The preferred copolymers of butylene and propylene contain up to 30 wt% butylene.
The preferred terpolymers of propylene contain from 1 to 10, preferably from 2 to 6, wt% ethylene, from 80 to 97, preferably from 88 to 95, wt% propylene, and from 1. to 20, preferably from 2 to 15, wt% butene-1.
Preferably, the second layer contains an anti-blocking agent, or other additives. As noted above, such additives are not essential. Particularly good results have been obtained with silicone oil, EBS, GMS and montan wax. A preferred silicone oil is a polydialkylsiloxane.
When silicone oil is used there is some transfer of the silicone oil to the surface of the adhesive after the film has been wound onto a roll. However, despite this transfer good adhesion by the pressure sensitive adhesive coated surface was manifest.
Preferably the core layer comprises an oriented olefin polymer. The core layer desirably comprises a polymer of propylene, suitably homopolymeric polypropylene and preferably isotactic polypropylene.
The core layer may be provided with voids: more specifically, the core layer may be cavitated, for example, as disclosed in EP-A-0083495. A preferred cavitating agent is polybutylene terephthalate, especially as spherical particles.
The first layer comprises HDPE which has been treated to alter its surface properties. The first layer may comprise any of the materials described above with reference to the second layer. If desired, the first layer may be the same material as the second layer.
The surface treatments discussed above, with reference to the second aspect of the invention, may be achieved, for example, by subjecting the surface to corona discharge, to a flame or to oxidising chemicals; a flame treatment is preferred. Preferably, the surface is treated to a surface activity of at least 36 dynes/cm (36 mN/m) , more preferably to at least 40 dynes/cm (40 mN/m) .
In the second embodiment the core layer is preferably coextruded or extrusion coated with the first and second layers, and then the whole support is desirably biaxially oriented. The polymers can be brought to the molten state and coextruded from a conventional extruder through a flat sheet die, the melt streams being combined in an adapter prior to being extruded from the die. After leaving the die orifice, the thermoplastic polymeric film structure is chilled and the quenched sheet is then preferably reheated and oriented by stretching; for example, from 4 to 6 times in the machine direction at about 253°F (123°C) and, subsequently,, from 8 to 10 times in the transverse direction, at about 310°F (154°C) .
The pressure sensitive adhesive referred to above may be a hot melt adhesive, a solvent based adhesive or a water based adhesive. The invention may be used with any pressure sensitive adhesive used in the adhesive tapes of the prior art. Particular adhesives that may be used include rubber and acrylic based adhesives, which are described in detail in the prior art.
The following Examples illustrate the invention.
Example 1
Polypropylene homopolymer was fed into the feed hopper of a rotating screw extruder having a 2.5 inch (6.4 cm) diameter and an L:D ratio of 24:1. HDPE (density 0.952) was also fed into a satellite extruder having a 1.5 inch (3.8 cm) diameter and an L:D ratio of 20:1. The molten polyethylene was fed into the slot die fixed to the first extruder through an adaptor designed to ensure that the molten polyethylene stream covered both sides of the molten polypropylene stream. The multi-layer structure was then quenched onto a chill roll to form a cast film which was immediately quenched in a cold water bath and sequentially biaxially oriented on conventional equipment. During the orientation the quenched film was first reheated to about 253°F (123°C) and stretched 5 times the machine direction between differential speed rollers, and was then fed to a transverse orientor where it was heated to about 310°F (154°C) and stretched 8 times.
The film, comprising 0.6 μm HDPE skin, on both sides, was next cooled; and trimmed. Thereafter it was flame treated to > 48 dynes/cm on one side; and wound on a roll. Finally the film was tested, using the following procedure, to demonstrate release effect.
PROCEDURE :
A standard adhesive tape, containing a pressure sensitive adhesive was applied to the treated, or the untreated, side of the prepared film in the MD direction. This provides an adhesive coating on the prepared film, and gives the film a structure in accordance with the invention.
The samples were, or were not, stored 24 hours at 50°C. The peel force necessary to separate both the standard tape and the test film was measured at 300 mm/min with the film test and adhesive at 90° angle.
The transfer of adhesive was observed when peeling the samples at different angles (90° and 180°).
The measurements were performed 3 times, and the mean was taken. The results are shown in Table 1.
This test simulates what happens during unwinding a reel of tape composed of a support layer and a pressure sensitive adhesive applied to a treated surface of the support layer. Example 2 A film A was prepared using HDPE as the first layer; polypropylene as the core; and HDPE as the second layer. This film was produced by the same method as the film of example 1.
Example 3 A film B was prepared by the same method as in Example 1, but the second layer incorporated 12000 ppm of silicone oil.
Example 4
A film C was prepared by the same method as in Example 1, but the second layer incorporated 2000 ppm EBS.
Example 5 A film D was prepared by the same method as in Example 1, but the second layer incorporated 2000 ppm GMS.
Example 6
A film E was prepared by the same method as in Example 1, but the second layer incorporated 2000 ppm montan wax.
Example 7
The Films A to E were tested using a similar procedure to example 1: a standard adhesive tape was applied uniformly to the untreated side of each film A to E, and the release force was measured on the untreated side at 300 mm/min and with the test tape at 90°, 135° and 180° angles. The percentage transfer of adhesive when peeling the samples was also observed. The following films were also tested : Film F - Reference tape 35 μm Film G - PP terpolymer
Film H - PP terpolymer + 20000 ppm EBS Film I - PP terpolymer + 2000 ppm GMS Film J - PP terpolymer + 2000 ppm montan wax The release forces were measured 5 times, and the mean was taken. The results are shown in table 2 . TABLE 1
FILM UNTREATED TREATED Release Force Adh. Transfer Release Force Adh. Transfer (g/25mm) 90° 180° (g/25mm) 90° 180°
Experimental Film 201 - X 561 - X
Reference Films: Commercial OPP (28 MB 250) 599 X 598 Clear PVC (40 μm) 231 208 Yellow PVC (35 μ ) 137 139
After 24 Hours Storage at 50°C: Experimental Film 265 X 666 X
Reference Films:
Commercial OPP (28 MB 250) 492 X 752 Clear PVC (40 μm) 403 334 Ynllow PVC (35 μm) 376 358
TABLE 2
Film ANGLE 90° Force/g/25cm Transfer
A 265 0% B 175 0% C 305 0% D 315 0%
E 315 0% F 600 80% G 485 0% H 565 0% τ 595 0%
J 570 0%
The results in Table 2 show that the film structure according to the invention can be readily unwound from the roll, even without a release film; and that it is more readily unwound, with less adhesive transfer, than film structures of the prior art. It was also noted that the film structure of the present invention can be unwound with less raise than the film structures of the prior art.

Claims

1. A thermoplastic polymeric film structure comprising a support which is coated with a pressure sensitive adhesive on a first surface thereof, wherein a second surface of the support, opposite to the first surface, comprises high density polyethylene (HDPE) .
2. A film structure according to claim 1, wherein said first surface has been treated to alter its surface properties.
3. A film structure according to claim 2, wherein said surface treatment comprises flame treatment.
4. A film structure according to any preceding claim, wherein the support is cavitated.
5. A film structure according to any preceding claim, wherein the support comprises a single layer.
6. A film structure according to claim 5, wherein the support comprises HDPE.
7. A film structure according to claim 5 or 6, wherein said support has incorporated therein at least one additive comprising silicone oil, EBS, GMS and/or montan wax.
8. A film structure according to claim 7, wherein the silicone oil comprises a polydialkylsiloxane.
9. A film structure according to claim 1 , 2 , 3 or 4, wherein the support comprises three layers in a structure comprising a core layer, sandwiched between two other layers.
10. A film structure according to claim 9, wherein a first of said other layers is provided with the adhesive coating on the external surface thereof, and a second of said other layers comprises HDPE, the external surface of the second layer facing away from the adhesive coating.
11. A film structure according to claim 10, wherein the first layer comprises polypropylene or HDPE.
12. A film structure according to claim 10 or 11, wherein said second layer has incorporated therein at least one additive comprising silicone oil, EBS, GMS and/or montan wax.
13. A film structure according to claim 12, wherein the silicone oil comprises a polydialkylsiloxane.
14. A film structure according to any one of claims 9 to 13, where the core layer layer comprises isotactic polypropylene.
15. A film structure according to any one of claims 9 to 14, wherein at least two of the layers are formed by coextrusion.
16. A film structure according to any preceding claim, which is biaxially oriented.
17. A film structure according to any preceding claim, wherein the second surface is not subjected to any surface treatment.
18. Use of a film structure according to any preceding claim as a pressure sensitive adhesive tape.
19. A thermoplastic polymeric film structure which comprises:
(a) a support which is coated with a pressure sensitive adhesive on a first surface thereof, said surface comprising HDPE and having been surface treated prior to the application of said adhesive; and
(b) an anti-adhesive material incorporated in or coated on a second surface of the support opposite to the adhesive coating.
20. A film structure according to claim 19, wherein the second surface is not subjected to any surface treatment.
21. A film structure according to claim 19 or 20, wherein the first surface is subjected to flame treatment.
22. A film structure according to claim 19, 20 or 21, wherein the pressure sensitive adhesive is a hot melt adhesive.
23. A film structure according to any one of claims 19 to 22, wherein the anti-adhesive material comprises HDPE in the second surface of the support.
24. A film structure according to any one of claims 19 to 23, wherein the support comprises a single layer.
25. A film structure according to claim 24, wherein the support comprises HDPE, which acts as the anti-adhesive material.
26. A film structure according to claim 24 or 25, wherein said support has incorporated therein at least one additive comprising silicone oil, EBS, GMS and/or montan wax.
27. A film structure according to claim 26, wherein the silicone oil comprises a polydialkylsiloxane.
28. A film structure according to any one of claims 19 to 23, wherein the support comprises three layers in a structure comprising a core layer, sandwiched between two other layers.
29. A film structure according to claim 28, wherein a first of said other layers is provided with the adhesive coating on the external surface thereof, and a second of said other layers comprises HDPE, which acts as the anti-adhesive material, the external surface of the second layer facing away from the adhesive coating.
30. A film structure according to claim 29, wherein the first layer comprises polypropylene or HDPE.
31. A film structure according to claim 29 or 30, wherein said second layer has incorporated therein at least one additive comprising silicone oil, EBS, GMS and/or montan wax.
32. A film structure according to claim 31, wherein the silicone oil comprises a polydialkylsiloxane.
33. A film structure according to any one of claims 28 to 32, wherein the core layer layer comprises isotactic polypropylene.
34. A film structure according to any one of claims 28 to 33, wherein at least two of the layers are formed by coextrusion.
35. A film structure according to any one of claims 19 to 34, which is biaxially oriented.
36. Use of a film structure according to any one of claims 19 to 35 as a pressure sensitive adhesive tape.
EP94921659A 1993-07-22 1994-07-19 Pressure sensitive adhesive film Withdrawn EP0710266A1 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
GB9315201 1993-07-22
GB939315201A GB9315201D0 (en) 1993-07-22 1993-07-22 Adhesive films
PCT/EP1994/002381 WO1995003368A1 (en) 1993-07-22 1994-07-19 Pressure sensitive adhesive film

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EP0710266A1 true EP0710266A1 (en) 1996-05-08

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EP94921659A Withdrawn EP0710266A1 (en) 1993-07-22 1994-07-19 Pressure sensitive adhesive film

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EP (1) EP0710266A1 (en)
JP (1) JPH09500670A (en)
KR (1) KR960703996A (en)
CA (1) CA2167536A1 (en)
GB (1) GB9315201D0 (en)
WO (1) WO1995003368A1 (en)

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NL1002380C2 (en) * 1996-02-19 1997-08-20 Sallmetall Bv Cover foil.
NL1002551C2 (en) * 1996-03-08 1997-01-31 Johannes Antonius Maria Reinde Transparent adhesive protective laminated covering film for application to a substrate - has a top layer which does not adhere to the outer surface of the bottom layer when the film is on a roll
NL1003602C2 (en) * 1996-07-16 1998-01-21 Johannes Antonius Maria Reinde Cover foil.
NL1003601C2 (en) * 1996-07-16 1998-01-21 Johannes Antonius Maria Reinde Cover foil.
NL1006592C2 (en) * 1996-07-16 1998-01-21 Sallmetall Bv Light-transmitting foil for application to surface carrying information
KR100473402B1 (en) * 2002-01-28 2005-03-08 신호상 Biocide Polymer
JP2008208173A (en) * 2007-02-23 2008-09-11 Nitto Denko Corp Surface protecting sheet

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Publication number Priority date Publication date Assignee Title
US4173676A (en) * 1976-12-28 1979-11-06 Toyo Kagaku Kabushiki Kaisha Adhesive tape
DE3501726A1 (en) * 1985-01-19 1986-07-24 Hoechst Ag, 6230 Frankfurt POLYPROPYLENE TAPE
DE9305300U1 (en) * 1993-04-07 1993-06-09 Hoechst Ag, 6230 Frankfurt, De

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Title
See references of WO9503368A1 *

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WO1995003368A1 (en) 1995-02-02
GB9315201D0 (en) 1993-09-08
KR960703996A (en) 1996-08-31
CA2167536A1 (en) 1995-02-02

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