WO2015019062A1 - Pellicule anti-adhérente - Google Patents

Pellicule anti-adhérente Download PDF

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Publication number
WO2015019062A1
WO2015019062A1 PCT/GB2014/052362 GB2014052362W WO2015019062A1 WO 2015019062 A1 WO2015019062 A1 WO 2015019062A1 GB 2014052362 W GB2014052362 W GB 2014052362W WO 2015019062 A1 WO2015019062 A1 WO 2015019062A1
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WO
WIPO (PCT)
Prior art keywords
release liner
release
skin layer
liner according
modulus
Prior art date
Application number
PCT/GB2014/052362
Other languages
English (en)
Inventor
Simon Read
Original Assignee
Innovia Films Limited
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 Innovia Films Limited filed Critical Innovia Films Limited
Publication of WO2015019062A1 publication Critical patent/WO2015019062A1/fr

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    • 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
    • B32B25/00Layered products comprising a layer of natural or synthetic rubber
    • B32B25/04Layered products comprising a layer of natural or synthetic rubber comprising rubber as the main or only constituent of a layer, which is next to another layer of the same or of a different material
    • B32B25/08Layered products comprising a layer of natural or synthetic rubber comprising rubber 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
    • B32B25/00Layered products comprising a layer of natural or synthetic rubber
    • B32B25/16Layered products comprising a layer of natural or synthetic rubber comprising polydienes homopolymers or poly-halodienes homopolymers
    • 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
    • B32B27/28Layered products comprising a layer of synthetic resin comprising synthetic resins not wholly covered by any one of the sub-groups B32B27/30 - B32B27/42
    • B32B27/283Layered products comprising a layer of synthetic resin comprising synthetic resins not wholly covered by any one of the sub-groups B32B27/30 - B32B27/42 comprising polysiloxanes
    • 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
    • B32B27/00Layered products comprising a layer of synthetic resin
    • B32B27/34Layered products comprising a layer of synthetic resin comprising polyamides
    • 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
    • B32B27/36Layered products comprising a layer of synthetic resin comprising polyesters
    • 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
    • B32B7/02Physical, chemical or physicochemical properties
    • B32B7/022Mechanical properties
    • 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
    • C09J7/40Adhesives in the form of films or foils characterised by release liners
    • C09J7/401Adhesives in the form of films or foils characterised by release liners characterised by the release coating composition
    • 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
    • C09J7/40Adhesives in the form of films or foils characterised by release liners
    • C09J7/403Adhesives in the form of films or foils characterised by release liners characterised by the structure of the release feature
    • 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
    • B32B2250/00Layers arrangement
    • B32B2250/033 layers
    • 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
    • B32B2250/00Layers arrangement
    • B32B2250/24All layers being polymeric
    • 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
    • B32B2255/00Coating on the layer surface
    • B32B2255/10Coating on the layer surface on synthetic resin layer or on natural or synthetic rubber layer
    • 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
    • B32B2255/00Coating on the layer surface
    • B32B2255/24Organic non-macromolecular coating
    • 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
    • B32B2255/00Coating on the layer surface
    • B32B2255/26Polymeric coating
    • 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
    • B32B2274/00Thermoplastic elastomer 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
    • B32B2307/00Properties of the layers or laminate
    • B32B2307/50Properties of the layers or laminate having particular mechanical properties
    • B32B2307/546Flexural strength; Flexion stiffness
    • 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
    • B32B2307/70Other properties
    • B32B2307/716Degradable
    • B32B2307/7163Biodegradable
    • 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
    • B32B2405/00Adhesive articles, e.g. adhesive tapes
    • 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
    • B32B2519/00Labels, badges
    • 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
    • C09J2423/00Presence of polyolefin
    • C09J2423/10Presence of homo or copolymers of propene
    • C09J2423/106Presence of homo or copolymers of propene in the substrate
    • 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
    • C09J2427/00Presence of halogenated polymer
    • C09J2427/005Presence of halogenated polymer in the release coating
    • 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
    • C09J2467/00Presence of polyester
    • C09J2467/006Presence of polyester in the substrate
    • 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
    • C09J2483/00Presence of polysiloxane
    • C09J2483/005Presence of polysiloxane in the release coating
    • 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
    • C09J2491/00Presence of oils, fats or waxes
    • C09J2491/005Presence of oils, fats or waxes in the release coating

Definitions

  • the present invention relates to release liners. More specifically, it relates to release liners for use in adhesive labelling or packaging film.
  • Release liners are used in a variety of applications.
  • release liners are used with adhesive labels, for example pressure sensitive adhesive Iabels, and with packaging films.
  • Release liners are generally made up of a substrate and a release coating. Typical release coatings are formed from waxes, silicones or fluoropoiymers. The release coating aids the removal of the release liner from the adhesive surface to which it is attached.
  • the thickness of the release coating affects the release force i.e. the force required to remove the release liner from the adhesive surface to which it is attached. As the thickness of the release coating increases, there is a decrease in the release force until a minimum is reached. After this point, a further increase in the thickness of the release coating results in the release force either increasing or remaining constant. It is understood that the change in release force as thickness is changed, is due to deformation of the release coating rather than its surface chemistry.
  • release liners by applying a release coating to a substrate using wet-chemical coating processes, for example solvent-based wet- chemical coating or aqueous-based wet-chemical coating.
  • solvent-based wet-chemical coating involves the use of volatile organic compounds which are
  • US 4,859,511 describes a release sheet formed on paper, nonwoven fabric, polymeric film or extrusion-coated paper substrates,
  • the release sheet has a low polar surface energy hydrocarbon undercoating of low elastic modulus interposed between the substrate and a silicone release coating.
  • the silicone release coating is applied neat or from a solvent using offset gravure, direct gravure or multiple roll.
  • WO 94/13474 describes a silicone release film comprising a biaxially oriented PENB8 film having a coating thereon in an amount sufficient to act as a silicone release film.
  • the coating comprises glycidoxy silane and an aqueous based thermosetting silicone release composition.
  • release liners have been manufactured using atmospheric plasma processes to deposit a release coating onto a substrate. This avoids the use of harmful volatile organic compounds and can be run as a continuous process.
  • EP 1 242 515 describes a method for forming a coating on a substrate surface which coating comprises SiOx groups by plasma treatment of the surface, wherein the substrate comprises a blend of an organic polymeric material and 25% by weight or less of an organosilicon-containing additive which is substantially non-miscible with the organic polymeric material
  • EP 1 978 067 describes a release liner for use in a pressure-sensitive adhesive sheet comprising a release layer on a substrate, wherein the release liner is obtainable by a process comprising the steps of: providing a substrate; producing an atmospheric pressure plasma discharge in the presence of a gas; exposing the substrate to said atmospheric pressure plasma discharge; introducing a liquid aerosol comprising a precursor into said atmospheric pressure plasma discharge, thereby forming a release layer on the substrate; and curing the release layer on the substrate.
  • US 2008/0083811 describes a method of adjusting a surface characteristic of a substrate comprising: providing a substrate; and performing an atmosphere pressure plasma process on the surface of the substrate to form a film layer on the surface of the substrate, so as to adjust the surface energy of the substrate, wherein a process gas of the atmosphere pressure plasma process comprises a surface modifying precursor, a carrier gas and a plasma ignition gas, wherein the surface modifying precursor is selected from fluorosilane, polysiloxane and a combination thereof, and the ratio of fluorosilane to polysiloxane is between 0 and 1.
  • a release liner for use in adhesive labelling or packaging film, the release liner comprising a substrate layer and at least one skin layer, the modulus of the skin layer being less than that of the substrate layer and the skin layer having a nano-coating of a release compound thereon.
  • a 'Release liner' is a well-known term of art in the pressure sensitive adhesive label industry.
  • a 'release liner' typically comprises a substrate and a coating of a release compound which provides a release effect against an adhesive surface to which it is attached, thus aiding the removal of the release liner from the adhesive surface.
  • the term 'nano-coating' may mean a coating with a thickness up to about 100nm, for example up to about 75nm, about 50nm or about 25nm, or with a thickness of from about 1 nm to about IQOnm, for example from about 1 nm to about 75nm, from about 1 nm to about 50nm or from about 1nm to about 25nm.
  • the nano- coating may have a thickness of from about 1 nm to about 20 nm, from about 1 nm to about 15 nm. from about 1 nm to about 10 nm, or from about 1 nm to about 5 nm.
  • the release force of the release liner is not significantly affected by the thickness of the nano-coating. Rather, it has surprisingly been found that the release force is affected by changing the modulus (i.e. the Young's modulus) of the skin layer with respect to the substrate layer. In particular, it has been found that a release liner with a reduced release force can be obtained by using a skin layer with a modulus less than that of the substrate layer, This is advantageous since the lower the release force, the more easily the release liner is removed from the adhesive surface to which it is attached.
  • the release compound may comprise one or more of a wax, for example microcrystalline wax, a silicone for example poly(dimethyl siloxane), and a fluoropolymer for example polytetrafluoroethylene (PTFE).
  • the release compound comprises a silicone. More preferably, the release compound comprises poly(dimethyl siloxane), poly ⁇ dimethyl dichloro silane), poly ⁇ divinyl si!ane), poly ⁇ diphenyl siloxane), poly ⁇ phenylmethyl siloxane), 1 ,3-tetraphenyl 1 ,3-dimethyl disiloxane, and/or 1 ,3 ⁇ diphenyl 1 ,2-tetramethyl disiloxane. Yet more preferably, the release compound comprises poly(dimethyl siloxane),
  • the skin layer may comprise an elastomer.
  • the elastomer is a rubber.
  • the rubber may comprise an ethylene-propylene copolymer (EPM), an ethylene propylene-diene monomer copolymer (EPDM), polybutadiene, polyisoprene, a styrene-butadiene copolymer, a styrene-isoprene copolymer, a urefhane, a polyester and/or mixtures or blends thereof.
  • the skin layer comprises an ethylene- propylene copolymer, an ethylene propylene diene monomer copolymer and/or amorphous polyester.
  • the skin layer may have a thickness of from about 0.01 pm to about 10pm.
  • the skin layer has a thickness of from about 0.1 pm, about 0.2pm, about Q,3pm, about 0.4pm, about 0.5pm, about 0.55pm, about 0,6pm, about ⁇ , ⁇ , about 0.7pm, about 0.75pm, about 0.8pm, about 0.85pm, about 0.9pm or about 0.95 ⁇ ; to about 1 ⁇ , about ⁇ , about 2pm, about 2,5 ⁇ , about 3 ⁇ , about 3.5 ⁇ % about 4 ⁇ , about 4.5 ⁇ or about 5pm.
  • the skin layer may have a thickness of from about 0.1 ⁇ to about ⁇ , from about ⁇ . ⁇ to about ⁇ ⁇ , from about QJprn to about 2 m or from about 0.8 m to about 1 ,5pm.
  • the release force of the release liner may be affected by the thickness of the skin layer. More specifically, it has been found that the above-identified ranges of skin layer thickness may provide a release liner with an optimum release force. Varying the skin layer thickness within the above-identified ranges may cause a slight increase or decrease in the release force, or the release force may remain the same However, it has been found that if the skin layer thickness exceeds 10 ⁇ (and in some cases 5pm, depending on the composition of the skin layer), the release force of the release liner may increase to an unsatisfactory level.
  • the substrate layer may comprise a polyolefin, for example polyethylene, polypropylene, polybutylene, mixtures, blends or copolymers thereof; a polyester, for example polyethylene terephthalate; a polyamide, for example nylon; a polyurethane; a polyvinyl halide, for example polyvinyl chloride; an acetate and/or a biopoiymer, for example cellulose and/or its derivatives, polylactic acid or polyhydroxyalkanoate.
  • a polyolefin for example polyethylene, polypropylene, polybutylene, mixtures, blends or copolymers thereof
  • a polyester for example polyethylene terephthalate
  • a polyamide for example nylon
  • a polyurethane for example polyvinyl halide
  • a biopoiymer for example cellulose and/or its derivatives, polylactic acid or polyhydroxyalkanoate.
  • the substrate layer comprises polypropylene or polyethylene terephthalate.
  • the release !iner may be formed by any process known in the art, including, but not limited to, cast sheet, cast film, or blown film.
  • the skin layer may be coextruded or laminated onto the substrate layer.
  • the skin layer may be applied by coating techniques, including extrusion coating.
  • the substrate may be provided with additional layers on either side provided that the skin layer is available to receive the release compound.
  • the substrate layer may comprise a biaxially orientated polypropylene (BOPP) film, which may be prepared as a balanced film using substantially equal machine direction and transverse direction stretch ratios, or can be unbalanced, where the film is significantly more orientated in one direction ⁇ MD or TD).
  • Sequential stretching can be used, in which heated rollers effect stretching of the film in the machine direction and a stenter oven is thereafter used to effect stretching in the transverse direction.
  • simultaneous stretching for example, using the so-called bubble process, or simultaneous draw stenter stretching may be used.
  • the release liner of the present invention can be of a variety of thicknesses depending on the application requirements.
  • the release liner may be from about 5pm, about 10 m, about 15pm, about 20pm, about 25pm, about 30pm to about 40pm, about 50pm, about 75pm, about 100pm, about 125pm, about 150pm, about 200pm or about 250pm.
  • the substrate layer may have a modulus in the range of from about 0.1 GPa to about 10 GPa. More specifically, the substrate layer may have a modulus in the range of from about 0,5 GPa to about 5 GPa, Even more specifically, the substrate layer may have a modulus in the range of from about 1 GPa to about 3 GPa.
  • Modulus is defined as the ratio of tensile stress to tensile strain as measured using a Tensometer.
  • Young's modulus (E) describes tensile elasticity, or the tendency of an object to deform along an axis when opposing forces are applied along the axis. It is often simply referred to as the elastic modulus.
  • the skin layer may have a modulus of at least about 1% less than the modulus of the substrate layer. More preferably, the skin layer has a modulus of at least about 5% less than the modulus of the substrate layer, More preferably still, the skin layer has a modulus of at least about 10%, at least about 20%, at least about 30%, at least about 40%, at least about 50%, at least about 80%, at least about 70%, at least about 80% or at least about 90% less than the modulus of the substrate layer.
  • the ratio of the modulus of the substrate layer to the modulus of the skin layer may be from 10-30:1 ; from 10-29:1 ; from 12-28:1 ; from 13-27:1 ; from 14-28:1 ; from 15- 25:1 ; or from 10-25:1.
  • a release liner with a reduced release force can be obtained by using a skin layer with a modulus less than that of the substrate layer,
  • release force is reduced due to an increase in the effective release angle as a result of skin layer deformation.
  • a skin layer with a lower modulus will deform more when a force is applied thereto, resulting in a greater effective release angle. Consequently, the release force required to remove the release liner from a surface is reduced.
  • the release force required to remove the release liner from a surface to which it is attached may be from about 0,01 g/cm to about 50 g/cm.
  • the release force is from about 0.1 g/cm, about 0.2 g/cm , about 0.3 g/cm, about 0.4 g/cm, about 0.5 g/cm, about 0.8 g/cm, about 0,7 g/cm, about 0.8 g/cm or about 0.9 g/cm; to about 1 g/cm, about 2 g/cm, about 3 g/cm, about 4 g/cm, about 5 g/cm, about 8 g/crn, about 7 g/cm, about 8 g/cm, about 9 g/cm or about 10 g/cm.
  • the release force may be from about 0.1 g/cm to about 3 g/cm, from about 0.1 g/cm to about 2 g/cm
  • the release force may be measured in one of two ways, namely, the low speed release force method or the high speed release force method.
  • Low speed release force is defined as the force required to separate a release liner from the adhesive coated material to which it is attached (or vice versa) at an angle of 180° and a jaw separation rate of 300mm/min.
  • the low speed release force can be determined using a tensile fester or similar machine.
  • Test strips with a width of 50mm and a length of at least 175mm (in the machine direction) are taken from a release liner sample.
  • the release liner test strips are placed in contact with the adhesive surface of the material and kept for 20 hours at
  • test strips 23°C ⁇ 2 under a pressure of 8.88kPa (70 g/cm 2 ) to ensure good adhesion therebetween. After storage in this manner, the test strips must be left at standard test conditions (i.e. 23°C ⁇ 2°C and 50% ⁇ 5% relative humidity) for at least 4 hours.
  • Each test strip is then fixed to the tensile tester plate using double sided tape such that the release liner can be peeled apart from the adhesive coated material at an angle of 180° (or vice versa)
  • the tensile tester is then set at a jaw separation rate of 300mm/min and five readings are taken at 10mm intervals from the centre section of the test strip. These five readings are averaged to give a low speed release force value usually expressed in cN/50mm width.
  • the low speed release force test method is outlined in the standard test FTfv 3 (published by RNAT),
  • High speed release force is defined as i) the force required to separate a release liner from the adhesive coated material to which it is attached or is) the force required to separate the adhesive coated material from the release liner, at an angle of 180° and a jaw separation rate between 10m/min and 300m/min. Note that i) and ii) will usually give different release forces.
  • Test strips with a width of 25mm and a length of at least 300mm (in the machine direction) are taken from a release liner sample.
  • the release liner test strips are placed in contact with the adhesive surface of the material and kept for 20 hours at 23X ⁇ 2°C under a pressure of 8,88kPa (70 g/cm 2 ) to ensure good adhesion therebetween. After storage in this manner, the test strips must be left at standard test conditions (i.e. 23 ⁇ 2°C and 50% ⁇ 5% relative humidity) for at least 4 hours.
  • each test strip is placed in the machine and the release liner is fixed in the load cell clamp. A protective strip is often used at this stage to prevent the adhesive sticking to the rollers in the drive mechanism.
  • the machine is set to the desired test speed and the test carried out.
  • Results for high speed release force are usually expressed as the peak or average for the test strip in units of cN/25mm width.
  • the high speed release force test method is outlined in the standard test FTM 4 (published by FI AT).
  • the substrate layer and/or the skin layer may be biodegradable and/or compostable. This is advantageous as the release liner will have a low carbon footprint.
  • the substrate layer and/or the skin layer may be recyclable.
  • the entire release liner may be recyclable.
  • Current release liners are often non- recyclable due to the presence of an unacceptably high amount of release compound in/on the liner.
  • the release liner of the present invention comprises a nano-coating of the release compound which results in a low dilution factor of the release compound. This may allow the entire release liner to be recycled.
  • the substrate layer and/or the skin layer may have a radio carbon content i.e. the substrate layer and/or skin layer may be formed, at least In part, from a renewable material.
  • the substrate layer and/or the skin layer may have a radio carbon content of at least about IGplvIC, or at least about 20plV1C t or at least about 30pMC » or at least about 40p C, or at least about SOpMC, or at least about OOpfvIC, or at least about 70pMC, or at least about 80pMC, or at least about 90plV1C, or at least about lOOpMC.
  • the release liner may have a low carbon footprint.
  • Release liners according to the present invention may be particularly useful in applications such as pressure sensitive adhesive labels/tapes/packaging films.
  • a process for the manufacture of a release liner for use in adhesive labelling or packaging film comprising the steps of: a, providing a release liner comprising a substrate layer and at least one skin layer; and
  • the nano-coating may be deposited on the skin layer using an atmospheric pressure plasma.
  • the atmospheric pressure plasma is a dielectric barrier discharge (DBD).
  • DBD dielectric barrier discharge
  • the DBD atmosphere will generally comprise an inert carrier gas such as a noble gas e.g. argon, or nitrogen.
  • a noble gas e.g. argon, or nitrogen.
  • the DBD atmosphere may further comprise at least one functional or reducing agent, for example acetylene, hydrogen or silane.
  • the functional or reducing agent may be present in the DBD atmosphere in an amount of from about 10 ppm to about 20000 ppm.
  • the functional or reducing agent is present in the DBD atmosphere in an amount of from about 200 ppm to about 5000 ppm.
  • the DBD atmosphere may comprise at least one oxidising agent such as oxygen, ozone, carbon dioxide, carbon monoxide, nitric and nitrous oxides or sulphur oxide, dioxide or trioxide.
  • the oxidising agent may be present in the DBD atmosphere in an amount of from about 10 ppm to about 20000 ppm.
  • the oxidising agent is present in the DBD atmosphere in an amount of from about 200 ppm to about 5000 ppm.
  • the DBD atmosphere may additionally comprise at least one cross-linker, for example, an unsaturated hydrocarbon such as ethylene or propylene.
  • the cross-linker may be present in the DBD atmosphere in an amount of from about 10 ppm to about 1000 ppm.
  • the cross-linker is present in the DBD atmosphere in an amount of from about 50 ppm to 200 ppm,
  • the process may additionally comprise the step of feeding a release compound precursor into the DBD.
  • the release compound precursor may be a liquid which is vaporised prior to entering the DBD.
  • the release compound precursor may comprise a silicone.
  • the release compound precursor comprises hexamethyldisiloxane and/or tetramethyldisiloxane. It is believed that these release compound precursors polymerise in the DBD and are deposited on the surface of the skin layer as polydimethylsiloxane.
  • the release compound precursor may be present in an amount of from about 10 ppm to about 20000 ppm. Preferably, the release compound precursor is present in an amount of from about 200 ppm to about 5000 ppm.
  • the release liner may be provided as a web.
  • the process may additionally comprise the step of feeding a section of the release liner web into the DBD such that at least one surface of the release liner comes into contact with the DBD.
  • the at least one surface of the release liner is the skin layer.
  • the process rrsay further comprise the step of removing the section of the release liner web from the DBD, which may be achieved by winding the web onto a roller. As the section of the release liner web is removed from the DBD, a further section of the web may simultaneously be fed into the DBD. Thus, the process may be run continuously.
  • the same section of the release liner web may be passed through the DBD multiple times, for example twice or three times. This may allow the thickness of the nano- coating to be increased.
  • a pressure sensitive adhesive label comprising a release liner according to the first aspect of the present invention, and a label comprising an adhesive layer, wherein the label is attached to the release liner via the adhesive layer.
  • an article labelled with the pressure sensitive adhesive label according to the third aspect of the present invention.
  • Figure 1 is a schematic representation of how the effective release force is altered when the modulus and/or thickness of the skin layer changes.
  • Figure 1 schematically shows four different release liners. All of the release liners comprise a substrate layer 1, a skin layer and a nano-coating of release compound (not shown) thereon.
  • skin !ayer 2 has a high modulus which is equal to or greater than the substrate layer 1.
  • the effective release force at 90° is shown by arrow 3.
  • skin layer 4 is composed of the same material as skin layer 2 but the thickness of the skin layer has been increased, However, the effective release force at 90° shown by arrow S is the same as that of the top left release liner.
  • the skin layer 6 has a low modulus which is less than that of the substrate layer.
  • Deformation 8 of the skin layer S occurs when a force is applied to the skin layer. Due to deformation of the skin layer S, the effective release angle is greater than 90°C. As a result, the effective release force at 90°C is less than that of the previously discussed release liners, as shown by arrow 7.
  • the skin layer 9 is composed of the same material as skin layer 6 but the thickness of the skin layer has been increased.
  • the effective release force at 90°, shown by arrow 10, is smaller than release force 7. This is due to greater deformation 11 of the low modulus skin layer 9 which in turn creates an even larger effective release angle.
  • a release liner having a substrate layer of polypropylene homopolymer and coextruded skin layers of polyethylene/polypropylene/polybutylene random terpolymer each having a thickness of approximately 1 pm t was manufactured by means of a bubble process.
  • the three-layer release liner had an overall thickness of 30 ⁇ .
  • the release liner was fed into a DBD with an atmosphere of nitrogen and argon, A small amount of vaporised hexamethyl disiioxane was injected into the plasma discharge which resulted in a nano-coating of poly(dimethyl siloxane) release compound being deposited on one of the outer skin layers of the release liner.
  • Example 1 DBD treated at 85w.min/m 2 and a speed of SOm/msn, in an atmosphere of 400 ppm HDMSO in nitrogen.
  • Example 2 DBD treated at 85w.min/m 2 and a speed of SOm/ in, in an atmosphere of 200 ppm HDMSO in nitrogen.
  • Each coated release liner was tested to determine its release force using the low speed release method.
  • An adhesive tape as can be purchased from Tesa R TM, was attached to the nano-coated surface of the release liner. The tape was then pulled vertically upwards at a 90° angle (rather than 180°) and the force required to remove the tape after 30 mm, 40 mm and 50 mm (of the tape had been detached) was recorded along with the force average required. The force was measured using an instron tensometer fitted with a load cell of 10 N. An angle of 90 c was used as this is more applicable to PSA bottie labelling than an angle of 180°. In theory, the force average i.e.
  • the average force required to remove the entire length of the tape should be equal to the force required at any particular point along the tape. However, in practice this is not the case due to several factors. In particular, the unevenness of the tape adhesive, the varying pressure applied to adhere the tape to the release liner, and the amount of time lapsed between applying the tape to the release iiner and testing the release force. All of these factors cause variation in the degree of adhesion of the tape to the release Iiner and thus, the measured release force.
  • the release finer is subsequently fed into a DBD with an atmosphere of nitrogen and argon.
  • a small amount of vaporised hexamethyl disiloxane is injected into the plasma discharge which results in a nano-coating of poly(dimethyl siloxane) release compound being deposited on one of the outer skin layers of the release liner.
  • Example 3 DBD treated at 85w.min/m 2 and a speed of SOm/min, in an atmosphere of 400 ppm HDMSO in nitrogen.
  • Example 4 DBD treated at 85w.min/m 2 and a speed of SOm/min, in an atmosphere of 200 ppm HDfvlSO in nitrogen.
  • Each coated release liner is tested to determine its release force. This is achieved in the same manner as for Examples 1 and 2.

Landscapes

  • Engineering & Computer Science (AREA)
  • Mechanical Engineering (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Laminated Bodies (AREA)

Abstract

L'invention concerne une pellicule anti-adhérente à utiliser dans l'étiquetage adhésif ou le film d'emballage, pellicule anti-adhérente comprenant une couche de substrat et au moins une couche de peau, le module de la couche de peau étant inférieure à celui de la couche de substrat et la couche de peau comprenant sur sa surface un nano-revêtement d'un composé de libération.
PCT/GB2014/052362 2013-08-09 2014-07-31 Pellicule anti-adhérente WO2015019062A1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GBGB1314333.4A GB201314333D0 (en) 2013-08-09 2013-08-09 Release Liner
GB1314333.4 2013-08-09

Publications (1)

Publication Number Publication Date
WO2015019062A1 true WO2015019062A1 (fr) 2015-02-12

Family

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Application Number Title Priority Date Filing Date
PCT/GB2014/052362 WO2015019062A1 (fr) 2013-08-09 2014-07-31 Pellicule anti-adhérente

Country Status (2)

Country Link
GB (1) GB201314333D0 (fr)
WO (1) WO2015019062A1 (fr)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2960054A1 (fr) * 2014-06-26 2015-12-30 Taghleef Industries SPA Films traité en surface à base de polypropylène
EP3505880A1 (fr) * 2017-12-29 2019-07-03 UPM Raflatac Oy Collecte de complexes adhésifs usagés
WO2019154976A1 (fr) 2018-02-09 2019-08-15 Coating Plasma Innovation Film de protection a base de silicium pour adhesif, son procede de fabrication et ses utilisations
CN112898857A (zh) * 2021-01-20 2021-06-04 南方科技大学 一种高分子压力敏感漆及其制备方法和应用
CN113015623A (zh) * 2018-12-11 2021-06-22 三菱化学株式会社 脱模膜

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5372669A (en) * 1985-02-05 1994-12-13 Avery Dennison Corporation Composite facestocks and liners
US20070231571A1 (en) * 2006-04-04 2007-10-04 Richard Lane Pressure sensitive adhesive (PSA) laminates
US20130004749A1 (en) * 2009-11-20 2013-01-03 Encai Hao Surface-modified adhesives

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5372669A (en) * 1985-02-05 1994-12-13 Avery Dennison Corporation Composite facestocks and liners
US20070231571A1 (en) * 2006-04-04 2007-10-04 Richard Lane Pressure sensitive adhesive (PSA) laminates
US20130004749A1 (en) * 2009-11-20 2013-01-03 Encai Hao Surface-modified adhesives

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2960054A1 (fr) * 2014-06-26 2015-12-30 Taghleef Industries SPA Films traité en surface à base de polypropylène
EP3505880A1 (fr) * 2017-12-29 2019-07-03 UPM Raflatac Oy Collecte de complexes adhésifs usagés
WO2019154976A1 (fr) 2018-02-09 2019-08-15 Coating Plasma Innovation Film de protection a base de silicium pour adhesif, son procede de fabrication et ses utilisations
CN113015623A (zh) * 2018-12-11 2021-06-22 三菱化学株式会社 脱模膜
CN113015623B (zh) * 2018-12-11 2023-09-15 三菱化学株式会社 脱模膜
CN112898857A (zh) * 2021-01-20 2021-06-04 南方科技大学 一种高分子压力敏感漆及其制备方法和应用

Also Published As

Publication number Publication date
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