• 专利附录
  • 专利说明
  • 权利要求
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    • 专利摘要:
    1) multilayer film comprising two thin layers D and E of a thermoplastic material bonded together by a continuous layer A consisting of a hot-melt self-adhesive composition comprising: - from 40 to 70% by weight of a block copolymer composition styrenics consisting of a mixture of diblock and triblock copolymers; and from 30 to 60% by weight of one or more tackifying resins of softening temperature of between 5 and 140 ° C .; said multilayer film being such that the adhesive layer A is: - connected to the layer D via a bonding layer B, and connected to the layer E via a bonding layer C, each of 2 layers B and C being respectively constituted by a composition comprising a polyethylene or polypropylene modified with a cyclic anhydride of an unsaturated acid having from 4 to 8 carbon atoms. 2) Method of manufacturing said film by coextrusion 3) Use of said film for the manufacture of resealable packages.
    公开号:FR3021250A1
    申请号:FR1454597
    申请日:2014-05-22
    公开日:2015-11-27
    发明作者:Christophe Robert；Christophe Notteau；Ludovic Sallet
    申请人:Bostik SA；
    IPC主号:
    专利说明:

    [0001] The present invention relates to a multilayer film comprising a layer consisting of an extrudable hot-melt self-adhesive composition, a method of manufacturing said film, and its use for the manufacture of packaging (or trays). ) reclosable, especially for the packaging of foodstuffs, especially perishable. Claims WO 02/064694, WO 12/045950, WO 12/045951 and WO 14/020243 disclose extrudable hot melt self-adhesive compositions for use in the manufacture of resealable packages (or trays).
    [0002] Reclosable packagings, for example in the form of trays or sachets, are used in the food industry and retail to package perishable goods, especially fresh products. Such packages are also described by the patent EP 1053952. After a first opening of the package, and consumption of a portion of the food product it contains, the consumer can manually close the package substantially hermetically and ensure by therefore, if necessary after refrigeration, preserve the remaining portion of the product. A succession of reopenings and reclosures is also possible. These packages generally comprise a container (or receptacle) and a cover-lid, which are fixed to each other hermetically by welding. The receptacle, more or less deep and relatively rigid, consists of a multilayer sheet (also called complex or composite sheet) having a minimum thickness of 200 μm, generally between 200 and 1000 μm. This sheet is thermoformed so as to have a planar base on which the food product rests and a periphery in the form of a flat strip. This periphery, generally parallel to the bottom, is bonded by welding to the flexible and flat seal, which consists of a multilayer film (also called composite or composite) generally of thickness between 40 and 150 pm, and which is sometimes referred to as the lidding film denomination.
    [0003] When opening the package, the lidding film is separated manually from the receptacle at the level of the plane band of the perimeter. This operation reveals an adhesive layer at the level of this flat strip, both on the cover strip and on the receptacle strip which were previously in contact. These two adhesive layers (continuous or discontinuous) "so-called girls" result from the rupture of an initial adhesive layer or "mother" or, optionally, its separation (or detachment) of one of the two layers of multilayer complex film which are adjacent to it. The initial adhesive layer is therefore one of the layers of said multilayer complex film which is itself an element comprised either in the composite sheet which constitutes the receptacle or, preferably, in the lidding film. The two adhesive layers girls who are present, after opening the package, on the strips located on the respective periphery of the receptacle and the lid are facing each other. Thus, it is sufficient to reposition the lid on the receptacle, according to their position in the package before opening, in order to bring the two strips of adhesive adhesive layers back into contact. A simple manual pressure then makes it possible to obtain the reclosing of the package. The adhesive composition which constitutes the mother and daughter adhesive layers is therefore necessarily a pressure sensitive adhesive (also called self-adhesive or PSA, of the English "Pressure Sensitive Adhesive").
    [0004] The extrudable self-adhesive compositions described in the above applications are hot melt compositions comprising a tackifying resin and a styrenic block copolymer including an elastomeric block. Self-adhesive hot-melt compositions are also commonly known as HMPSA, corresponding to the initials of the English translation "Hot Melt Pressure Sensitive Adhesive". They are solid substances at room temperature that contain neither water nor solvent. Applied in the molten state, they solidify during their cooling, thus forming an adhesive layer which provides the connection between the two thin layers of thermoplastic polymeric material to be assembled, while offering the corresponding packaging the advantageous opening properties and reclosing. Moreover, these hot-melt self-adhesive compositions (or HMPSA), which are prepared by hot mixing of their ingredients, also have the advantage of being able to be in the form of granules (between 1 and 10 mm in size) by means of an extrusion step carried out directly hot after the mixing step, for example by means of a 2-screw extruder provided with a tool for cutting the extruded product.
    [0005] Thanks to the granules thus obtained, the three-layer film which consists of the hot-melt self-adhesive composition layer and the two thin layers of thermoplastic polymeric material to be assembled, can be conveniently manufactured by coextrusion, for example by feeding a blowing device. bubble by the constituent materials of the 3 layers in the form of granules of size defined above. The ease of opening such packages is closely related to the properties of the PSA and more particularly to the force to be applied, when opening the package (hereinafter referred to as the first opening), to obtain the rupture of the parent adhesive layer and / or its separation from one of the two layers adjacent thereto in the multilayer composite film mentioned above. The ability of the package to close and the quality of the reclosing obtained (hereinafter referred to as first reclosing) are also important to have again a substantially hermetic packaging and thus able to ensure the preservation of its contents. The quality of the first reclosing is also closely related to the properties of the PSA. It is evaluated by the force that must be applied, during the re-opening (hereinafter referred to as the second opening), to obtain again the rupture and / or the detachment of the adhesive layer which has been formed by the repositioning 2 layers of adhesive girls, followed by the manual pressure applied on the periphery of the packaging. EP 1053952 discloses a resealable package with a container which comprises a complexable layer, an adhesive layer and a tearable sealing layer. This adhesive is a self-adhesive which is described very generally. US2013 / 0029553 discloses a multilayer film for resealable packages comprising a heat-sealable layer consisting of a specific amorphous polyethylene terephthalate, a PSA layer, and at least one bonding layer consisting of a copolymer of ethylene and acrylate. methyl. The application WO 12/045951 discloses a multilayer film comprising 2 thin layers of thermoplastic materials bonded together by a layer of an adhesive composition based on styrenic block copolymers, said layer having a thickness of between 7 and 300 μm. This multilayer film, which is suitable for the manufacture of resealable packages, makes it easier to open them, by lowering the force of first opening, while maintaining substantially the same quality of the subsequent resealing (or first reclosing).
    [0006] However, in the context of the constant improvement of resealable packaging proposed by the industry to the consumer, it now appears more and more necessary to improve the closing performance of said packaging. The present invention therefore aims to provide a multilayer film suitable for the manufacture of resealable packaging, which - while maintaining a first easy opening of the package - to improve the quality of its reclosing (or first reclosing), in order to provide the consumer with a more efficient way of preserving the remaining portion of the perishable food product. The invention therefore also aims to increase the second opening force, while maintaining the first opening force to an acceptable level. Another object of the present invention is to provide a multilayer film for achieving the above goals at room temperature, corresponding to the temperature at which the consumer proceeds to the opening and reclosing of the package. Another object of the present invention is to provide a multilayer film capable of being manufactured by coextrusion from raw materials packaged in the form of granules, in particular by bubble-blown coextrusion, for manufacturing purposes. a resealable packaging. It has now been found that these objects can be obtained, in whole or in part, by means of the multilayer film according to the invention which is described below. The first subject of the present invention is therefore a multilayer film comprising two thin layers D and E of a thermoplastic material bonded to one another by a continuous layer A which has a thickness ranging from 7 to 50 μm, and consists of by a hot-melt self-adhesive composition having a flow index (or MIT) ranging from 0.01 to 200 g / 10 minutes and comprising, based on the total weight of said composition: 40 to 70% by weight weight of a composition al of styrenic block copolymers comprising at least one elastomer block, said composition being constituted, on the basis of its total weight: from 30 to 90% by weight of at least one diblock copolymer chosen from the group comprising SI, SBI, SIB, SB, SEB, and SEP, and from 10 to 70% by weight of at least one triblock copolymer selected from the group consisting of SIS, SIBS, SBS, SEBS and SEPS; the total styrenic unit content of said composition al ranging from 10 to 40% by weight based on the total weight of α1; and from 30 to 60% by weight of one or more tackifying resins a2 having a softening temperature of from 5 to 140 ° C; said multilayer film being further characterized in that the adhesive layer A is: - connected to the layer D via a bonding layer B, and - connected to the layer E by means of a layer of bond C, each of the two layers B and C consisting respectively of a composition b and c comprising a polyethylene or polypropylene modified with a cyclic anhydride of an unsaturated acid having from 4 to 8 carbon atoms. In addition to the percentages indicated above, all the percentages generally used in the present text to designate the amounts of ingredients of a composition correspond, in the absence of an indication to the contrary, to percentages expressed by weight on the basis of the total weight of said composition. The characteristics of the layers A, B, C, D and E included in the multilayer film according to the invention will now be described in greater detail below.
    [0007] Description of the composition constituting the adhesive layer A: The composition a which is comprised in the composition HMPSA constitutive of the adhesive layer A comprises one or more block copolymers styrenic, weight average molecular weight Mw generally between 50 kDa and 500 kDa.
    [0008] These styrenic block copolymers consist of blocks of different polymerized monomers including at least one polystyrene block, and are prepared by radical polymerization techniques. In the absence of any indication to the contrary, the weight average molecular weights MW given in this text are expressed in dalton (Da) and are determined by Gel Permeation Chromatography, the column being calibrated with polystyrene standards. The triblock copolymers include 2 polystyrene blocks and an elastomeric block. They can take various structures: linear, star (also called radial), connected or comb. The diblock copolymers include 1 polystyrene block and 1 elastomeric block. The tri-block copolymers have the general formula: ABA (I) in which: A represents a non-elastomeric styrene block (or polystyrene), and B represents an elastomer block which may be: polyisoprene. The block copolymer then has the structure: polystyrene-polyisoprene-polystyrene, and for denomination: SIS; polyisoprene followed by a polybutadiene block. The block copolymer then has the structure: polystyrene-polyisoprene-polybutadiene-polystyrene, and for denomination: SIBS-polybutadiene. The block copolymer then has the structure: polystyrene-polybutadiene-polystyrene, and for denomination: SBS; hydrogenated polybutadiene totally or partially. The block copolymer then has the structure: polystyrene-poly (ethylenebutylene) -polystyrene and for denomination: SEBS; partially or completely hydrogenated polyisoprene. The block copolymer then has the structure: polystyrene-poly (ethylenepropylene) -polystyrene and for denomination: SEPS.
    [0009] The di-block copolymers have the general formula: A-B (II) in which A and B are as defined above. When the composition α1 comprises several triblock styrene copolymers, the latter being chosen from the group comprising SIS, SBS, SEPS, SIBS, SEBS, it is understood that said triblocks can belong to one or more of these groups. 5 families of copolymers. It is the same, mutatis mutandis, for the diblock copolymers. It is preferred to use a composition a1 comprising a triblock copolymer and a diblock copolymer having the same elastomer block, especially because such mixtures are commercially available. According to a particularly preferred embodiment, the content of diblock copolymer in the composition a may vary from 40 to 90%, preferably from 50 to 90%, even more preferably from 50 to 60%. According to a particularly advantageous embodiment of the composition constituting the layer A included in the multilayer film according to the invention, the composition a consists of a triblock copolymer SIS and a diblock copolymer SI. In this case the total styrenic unit content of the composition a1) preferably varies from 10 to 20%.
    [0010] The triblock copolymers included in the composition a1 preferably have a linear structure. Styrenic block copolymers with an elastomeric block, in particular of SI and SIS type, that can be used in composition a) are commercially available, often in the form of triblock / diblock mixtures. Kraton® D1113BT from Kraton and Quintac® 3520 from Zeon Chemicals are examples of compositions consisting of SIS and SI. Kraton® D1113BT is a composition having an overall styrenic unit content of 16%, consisting of 45% linear SIS triblock copolymer MW about 250 kDa, and 55% diblock copolymer SI MW about 100 kDa. . Quintac® 3520 is a composition consisting of 22% and 78% linear SIS (M, about 300 kDa) and SI (M, about 130 kDa) triblock, respectively, with a total styrenics is 15%. The composition HMPSA constitutive of the layer A also comprises one or more tackifying resins a2 having a softening temperature of between 5 and 140 ° C. The at least one tackifying resistor a2 which has a weight average molar mass MW generally between 300 and 5000 Da and is chosen in particular from: - (i) rosin of natural origin or modified origin, such as, for example, rosin extracted from pine gum, wood rosin extracted from tree roots and their hydrogenated, dehydrogenated, dimerized, polymerized or esterified derivatives by monoalcohols or polyols such as glycerol; (ii) resins obtained by hydrogenation, polymerization or copolymerization (with an aromatic hydrocarbon) of unsaturated aliphatic hydrocarbon mixtures having about 5, 9 or 10 carbon atoms derived from petroleum cuts; (iii) terpene resins generally resulting from the polymerization of terpenic hydrocarbons such as for example mono-terpene (or pinene) in the presence of Friedel-Crafts catalysts, optionally modified by the action of phenols; (iv) copolymers based on natural terpenes, for example styrene / terpene, alpha-methyl styrene / terpene and vinyl toluene / terpene. The temperature (or point) of softening of the tackifying resins used in the composition according to the invention may vary from 5 to 140 ° C. The softening temperature is determined in accordance with the ASTM E 28 standard test, the principle of which is as follows. A brass ring about 2 cm in diameter is filled with the resin to be tested in the molten state. After cooling to room temperature, the ring and the solid resin are placed horizontally in a thermostated bath of glycerine whose temperature can vary from 5 ° C per minute. A steel ball approximately 9.5 mm in diameter is centered on the solid resin disc. The softening temperature is -during the temperature rise of the bath at a rate of 5 ° C per minute- the temperature at which the resin disc flows 25.4 mm under the weight of the ball. According to a preferred variant, aliphatic resins belonging to categories (ii) or (iii) are used for which examples of commercially available resin may be mentioned: (ii) Escorez® 1310 LC available from Exxon Chemicals which is a resin obtained by polymerizing a mixture of unsaturated aliphatic hydrocarbons having about 5 carbon atoms, and having a softening temperature of 94 ° C and a Mw of about 1800 Da; Escorez® 5400 also from the company Exxon Chemicals which is a resin obtained by polymerization, then hydrogenation of a mixture of unsaturated aliphatic hydrocarbons having about 9 or 10 carbon atoms and having a softening temperature of 100 ° C. and a Mw about 570 Da; (iii) Dercolyte® S115 available from the company "Resinic and Terpenic Derivatives or DRT" which a terpene resin having a softening temperature of 115 ° C and an Mw of about 2300 Da.
    [0011] According to one preferred variant, the HMPSA composition constituting the layer A consists essentially of: 40 to 70% of the al composition of styrenic block copolymers; and from 30 to 60% of at least one tackifying resin a2 having a softening temperature of between 5 and 140 ° C.
    [0012] According to another preferred variant, the composition HMPSA constitutive of layer A comprises or consists essentially of: from 50 to 70% of the composition of styrenic block copolymers; and from 30 to 50% of at least one tackifying resin a2 having a softening temperature of between 5 and 140 ° C.
    [0013] According to another preferred variant, the composition HMPSA constituting the layer A may also comprise, in addition to the composition α1 and the tackifying resins α2, from 0.1 to 2% of one or more stabilizers (or -oxidative). These compounds are introduced to protect the composition from degradation resulting from a reaction with oxygen which is likely to be formed by the action of heat, light or residual catalysts on certain raw materials such as tackifying resins . These compounds may include primary antioxidants that trap free radicals and are generally substituted phenols such as Irganox® 1010 from CIBA. The primary antioxidants may be used alone or in combination with other antioxidants such as phosphites such as Irgafos® 168 also CIBA, or with UV stabilizers such as amines. The composition may also comprise a plasticizer, but in a quantity not exceeding 5%. A paraffinic and naphthenic oil (such as Primol® 352 from ESSO) optionally comprising aromatic compounds (such as Nyflex 222B) can be used as plasticizer. The composition may finally comprise inorganic or organic fillers, pigments or dyes. The flow index (or Melt Flow Index MIT) of the hot melt adhesive self-adhesive composition of layer A is measured at 190 ° C and for a total weight of 2.16 kg, in accordance with condition d) of ISO 1133. The MIT is the composition mass (previously placed in a vertical cylinder) which flows in 10 minutes through a die of fixed diameter, under the effect of a pressure exerted by a loaded piston having a total weight of 2.16 kg. In the absence of mention to the contrary, the MIT values given in this text have been measured under the same conditions. The hot melt adhesive compositions of layer A having an MIT ranging from 2 to 100 g / 10 minutes are more particularly preferred. Description of compositions b and c, respectively, of linking layers B and C: Link layers B and C are also referred to as "intermediate layers" or "tie layers". These two layers consist respectively of compositions b and c, which are identical or different, each comprising a polyethylene or polypropylene modified with a cyclic anhydride of an unsaturated dicarboxylic acid having from 4 to 8 carbon atoms. Maleic anhydride is a most preferred cyclic anhydride. The term "polyethylene modified" by said anhydride is meant to be a copolymer of ethylene and said anhydride, or a homopolymer or copolymer of ethylene grafted with said anhydride.
    [0014] The copolymers of ethylene and of anhydride are, for example, random copolymers comprising: a repeating unit derived from ethylene, a repeating unit derived from the cyclic anhydride, and optionally a repeating unit derived from an alpha-olefin which may have from 3 to 20 carbon atoms. The alpha-olefins used can be propylene, 1-butene, 1-hexene, 4-methyl-1-pentene, 1-octene, 1-decene, 1-tetradecene and 1-octadecene. . The copolymers of ethylene and anhydride may comprise from 0.3 to 20% by weight of the anhydride defined above, and - when the corresponding comonomer is present - from 20 to 30% by weight of alpha-olefin. The repeat unit derived from ethylene may be from about 20, 40 or 50% to about 70, 80, 90 or 95% by weight of the copolymer. Homopolymers or copolymers of polyethylene may include a linear polyethylene such as HDPE (High Density PolyEthylene), a linear low density polyethylene (LLDPE), very low or ultra low density (VLDPE or ULDPE), a branched polyethylene such as low polyethylene density. Such polyethylenes can be prepared by several methods, including polymerization in the presence of a Ziegler-Natta catalyst, metallocene catalyzed polymerization, radical polymerization.
    [0015] Grafted ethylene homopolymers (or copolymers) are prepared by reacting an ethylene (co) polymer already formed with the compound to be grafted by heating, with or without a free radical generating catalyst (such as an organic peroxide) and in the presence or absence of a solvent. None of the constituent atoms of the grafted radical, often added by a radical reaction, is incorporated in the main chain of the (co) ethylene polymer. The grafted radical is linked, as a pendant group, to certain repeating units of the (co) polymer main chain. The ethylene polymer grafted with maleic anhydride is either a homopolymer or a copolymer. Such a copolymer is, for example, a random copolymer comprising, in addition to the repeat unit derived from ethylene, a repeating unit derived from an alpha-olefin as defined above. It is preferred to use compositions b and c consisting essentially of polyEthylene modified with maleic anhydride, and most preferably LLDPE modified with maleic anhydride.
    [0016] Many polyethylenes modified with maleic anhydride are commercially available. Mention may thus be made of Bynel 4206 sold by DuPont, which is a LLDPE modified with maleic anhydride, or Orevac® 18360 marketed by Arkema and DuPont's Bynel 41E865, both LLDPE grafted with maleic anhydride. . According to a preferred variant, the modified polyethylene included in compositions b) and c) is a grafted ethylene homopolymer or copolymer. According to a variant which is also preferred, the compositions b and c of the layers B and C 10 are identical. Description of the Constitutive Composition of the D and E Layers: The adhesive layer A allows via the connecting layers B and C to ensure the connection between a complexable thin film D and a sealable and breakable thin film E. The diaper complexable can be complexed (or laminated) with other layers for the realization of the package, for example with a rigid layer for the realization of the receptacle. The sealable and breakable layer makes it possible to ensure, at the level of the periphery along which the receptacle is bonded by welding to the lid, the first opening of the package, by means of a breakable weakened zone. After opening, the weakened zone shows: - the mother adhesive layer on the seal strip and / or on the receptacle strip that were in contact in the closed package, and / or - 2 adhesive layers girls resulting from the rupture of the parent adhesive layer and located on the cap strip and / or the receptacle strip. The material that can be used to form the two layers D and E is generally a thermoplastic polymer (identical or different for the two layers) such as: polyethylene (PE), polypropylene (PP), a copolymer based on ethylene and propylene, polyamide (PA), polyethylene terephthalate (PET), or alternatively an ethylene-based copolymer such as, for example, a maleic anhydride graft copolymer, a copolymer of ethylene and vinyl acetate ( EVA), a copolymer of ethylene and vinyl alcohol (EVOH), a copolymer of ethylene and an alkyl acrylate such as methyl acrylate (EMA) or butyl (EBA), - polystyrene (PS), polyvinyl chloride (PVC), polyvinylidene fluoride (PVDF), lactic acid polymer (PLA), or polyhydroxyalkanoate (PHA).
    [0017] It is preferred to use to form the two layers D and E a polyolefinic material, and especially PE, and even more preferably a low density PE (also referred to as Low Density Polyethylene or LDPE). According to another variant embodiment, the multilayer film according to the invention comprises, in addition to the layers A, B, C, D and E, other thin layers necessary for producing the package, such as for example: rigid layer necessary for the mechanical strength of the receptacle, or - a printable layer, or - a barrier layer against oxygen, water vapor or carbon monoxide. The materials used to form said layers may be identical or different and generally comprise thermoplastic polymers which may be chosen from the polymers mentioned above for layers D and E. The thickness of layer A may preferably vary from at 25 μm, still more preferably from 10 to 20 μm. The thickness of the bonding layers B and C is generally between 1 and 10 μm, preferably between 2 and 8 μm. The thickness of the two layers D and E, as well as the other layers possibly used in the multilayer film according to the invention, may vary over a wide range from 5 to 150 μm. According to an alternative embodiment, the multilayer film according to the invention is a 5-layer film consisting of the adhesive layer A, the two intermediate layers B and C and the two outer layers D and E, according to the sequence D / B / A / C / E in which the sign "/" signifies that the faces of the layers concerned are in direct contact.
    [0018] The present invention also relates to a method of manufacturing the multilayer film as defined above, characterized in that it comprises the co-extrusion of the self-adhesive hot melt composition a, compositions b and c, and materials constituting the D layers. summer.
    [0019] Preferably, the compositions and materials constituting the layers A, B, C, D and E are fed into the coextrusion device in the form of granules with a size of between 1 and 10 mm, preferably between 2 and 5 mm. Thus, the self-adhesive composition used in the multilayer film according to the invention allows, in a particularly advantageous manner, to ensure both the properties required for said film and the possibility of a presentation of said composition. the shape of the granules mentioned above. The other layers possibly included in the multilayer film may be obtained either by incorporating into the co-extrusion device the corresponding constituent materials in the form of granules of the same size, or by a process of laminating the film directly from the co-extrusion material. extrusion, using for example a polyurethane adhesive. The adhesive composition can be prepared, in this form of granules, by simply mixing its ingredients while hot, between 150 and 200 ° C., preferably at about 160 ° C., by means of a 2-screw extruder provided with A tool for cutting the extruded product at the outlet of the die 20 The bubble blow coextrusion method (also known as "coextrusion by jacket blowing") is more particularly preferred. In a manner known to those skilled in the art, this process comprises: the melting, in separate extruders, of the compositions and materials constituting the layers A, B, C, D and E, then the passage of the corresponding flows through a set of annular and concentric dies, so as to form a tubular bubble with several layers, in the order corresponding to that desired for the final structure, then - the radial expansion (relative to the ring filial) and the stretching ( in the axial direction) of the bubble, then cooling of the bubble. The geometric characteristics of the dies, as well as the process parameters such as the radial expansion rate and the stretching speed are set so as to obtain the desired thickness for the various constituent layers of the multilayer film. In particular, reference is made to the description of the bubble blow coextrusion process in US2013 / 0029553. The present invention also relates to the use of the multilayer film as described above for the manufacture of resealable packages.
    [0020] The use for the manufacture of resealable trays is particularly advantageous, and according to a particularly preferred embodiment for the manufacture of the lidding film of these trays. The following examples are given purely by way of illustration of the invention, and can not be interpreted in any way to limit its scope.
    [0021] Example A (reference) Composition A of layer A A composition consisting of 59.5% Kraton® D1113BT, 25% by weight, was prepared as a viscous liquid. Escorez® 1310 LC, 15% Dercolyte® S115 and 0.5% Irganox® 1010 by simply mixing the ingredients at 160 ° C using a 2-screw extruder. An MFI of 57 g / 10 minutes is measured. Example B (reference): D / A / E trilayer film consisting of a layer A of the composition of Example A: This three-layer film is produced by means of a bubble blowing coextrusion pilot device operating in continuous, in which 3 extruders are fed: - for one, by the composition of Example A, and - for the other 2, by LDPE; the 3 compositions being in the form of granules with a size of about 4 mm. The parameters of the process are adjusted so as to produce a three-layer film consisting: as layer A, of a layer of thickness 15 μm consisting of the composition of example A, as a complexable thin layer D, a 30 μm thickness layer made of LDPE; as a sealable and breakable thin layer E, a layer of thickness 15 iam also made of LDPE.
    [0022] Among the parameters usually fixed, mention may be made of a radial expansion rate of the bubble equal to 3, a stretching speed of 7 m / minute and an overall flow rate of 11 kg / hour. The three-layer film thus obtained has a total thickness of 60 μm, a length of 50 μm and is packaged in the form of a coil of 250 mm width.
    [0023] T-Peel First Peel Force Measurement at 23 ° C: A sample in the form of a rectangular A4-size sheet (21 x 29.7 cm) was cut from the three-layer film thus obtained. The outer face of the complexable layer D of this sample is: firstly subjected to a corona surface treatment (by means of a plasma), then in a second complexed time (in other words laminated or laminated) on a PET film 23 μm thick using a solvent-based polyurethane adhesive and using a Mayer bar type coating apparatus.
    [0024] The rectangular sheet is then placed in press for 24 hours. Then, said rectangular sheet is folded along a line located in its middle and parallel to the short side of the rectangle, leading to bringing into contact with itself the sealable and breakable layer E. Partial sealing is then carried out by means of two heating jaws at 130 ° C., applied at a pressure of 6 bar for 1 second, so as to obtain rectangular-shaped sealed zones (8 cm in length and 1 cm in width). ) arranged perpendicular to the fold line. Each sealed area is cut to obtain a tensile test specimen in which the sealed area of 8 cm in length is extended (to that of its ends which is opposite to the fold line) by 2 strips of about 2 cm in length left free and unsealed. These two free bands are fixed on two attachment devices (called jaws) connected, respectively, to a fixed part and a movable part of a traction device which are located on a vertical axis. This traction device is a dynamometer. While a drive mechanism communicates to the movable portion a uniform speed of 300 mm / min leading to peeling of the sealed layers, the ends move progressively along a vertical axis at an angle of 180 °. A force sensor connected to said moving part measures the force supported by the test piece thus maintained. The measurement is carried out in a climatic room maintained at a temperature of 23 ° C. The strength obtained is shown in Table 1.
    [0025] Measurement of the second T-peel force at 23 ° C. The two parts of the preceding test piece are, after peeling, repositioned facing each other and placed in manual contact. They are then subjected to a pressure exerted by means of a 2 kg mass roll with which a round-trip movement is carried out in a direction parallel to the length of the test piece. This gives a tensile test piece of identical shape to that prepared for the previous peel test, which is then repeated. The strength obtained is shown in Table 1.
    [0026] Examples 1-3: 5-layer films D / B / A / C / E comprising a layer A consisting of the composition of Example A: Example B is repeated modifying the coextrusion process so as to add to the two layer bilayer film B and C having the same thickness of 5 μm and the same composition, namely a LLDPE modified with maleic anhydride as shown in Table 1.
    [0027] A film with 5 layers of total thickness equal to 70 μm is obtained. The 1st and 2nd opening forces are shown in Table 1. The 1st opening force results are greater than that obtained for Example B, but correspond to a completely acceptable reclosable package opening quality. The results obtained for the second opening force show a clear increase compared to Example B, which significantly indicates an improvement in the quality of the reclosure of the resealable package, following its first opening.
    [0028] Table 1 Example B Example 1 Example 2 Example 3 Material constituting the two bonding layers B and C Not relevant LLDPE grafted maleic anhydride LLDPE grafted maleic anhydride LLDPE modified maleic anhydride (Bynel® 41E865) (Orevac® 18360) (Bynel® 4206) Strength first opening (N / cm) 3.36 5.58 7.37 10.67 Second Strength 0.85 1.19 1.92 3.47 Aperture (N / cm)
    权利要求:
    Claims (15)
    [0001]
    REVENDICATIONS1. Multilayer film comprising two thin layers D and E of a thermoplastic material bonded together by a continuous layer A which has a thickness of from 7 to 50 nm, and is constituted by a hot-melt adhesive self-adhesive composition having a flow index (or 1 11I) ranging from 0.01 to 200 g / 10 minutes and comprising, based on the total weight of said composition: - from 40 to 70% by weight of a composition al of styrenic block copolymers comprising at least at least one elastomer block, said composition being constituted, on the basis of its total weight: from 30 to 90% by weight of at least one diblock copolymer chosen from the group comprising SI, SBI, SIB, SB, SEB, and SEP, and from 10 to 70% by weight of at least one triblock copolymer selected from the group consisting of SIS, SIBS, SBS, SEBS and SEPS; the total styrenic unit content of said composition al ranging from 10 to 40% by weight based on the total weight of α1; and from 30 to 60% by weight of one or more tackifying resins a2 having a softening temperature of from 5 to 140 ° C; said multilayer film being further characterized in that the adhesive layer A is: - connected to the layer D via a bonding layer B, and connected to the layer E via a bonding layer C, each of the two layers B and C consisting respectively of a composition b and c comprising a polyethylene or polypropylene modified with a cyclic anhydride of an unsaturated acid having from 4 to 8 carbon atoms.
    [0002]
    2. multilayer film according to claim 1, characterized in that the content of diblock copolymer in the composition al varies from 40 to 90%, preferably from 50 to 90%.
    [0003]
    3. Multilayer film according to one of claims 1 or 2, characterized in that the composition al consists of a triblock copolymer SIS and a diblock copolymer SI.
    [0004]
    4. Multilayer film according to one of claims 1 to 3, characterized in that the tackifying resins or a2 usable resins have average molecular weights by weight M, between 300 and 5000 Da and are chosen from: - (i) the Rosin of natural origin or modified, such as, for example, rosin extracted from pine gum, wood rosin extracted from tree roots and their hydrogenated derivatives, dehydrogenated, dimerised, polymerized or esterified with monoalcohols or polyols like glycerol; (ii) resins obtained by hydrogenation, polymerization or copolymerization (with an aromatic hydrocarbon) of unsaturated aliphatic hydrocarbon mixtures having about 5, 9 or 10 carbon atoms derived from petroleum cuts; (iii) terpene resins generally resulting from the polymerization of terpenic hydrocarbons such as for example mono-terpene (or pinene) in the presence of Friedel-Crafts catalysts, optionally modified by the action of phenols; (iv) copolymers based on natural terpenes, for example styrene / terpene, alpha-methyl styrene / terpene and vinyl toluene / terpene.
    [0005]
    5. multilayer film according to claim 4, characterized in that the tackifying resins or resins a2 are aliphatic resins belonging to categories (ii) or (iii).
    [0006]
    6. Multilayer film according to one of claims 1 to 5, characterized in that the compositions b and c comprise a polyethylene or polypropylene modified with maleic anhydride.
    [0007]
    7. Multilayer film according to one of claims 1 to 6, characterized in that the compositions b and c consist essentially of LLDPE modified with maleic anhydride.
    [0008]
    8. Multilayer film according to one of claims 1 to 7, characterized in that the compositions b and c are identical.
    [0009]
    9. multilayer film according to one of claims 1 to 8, characterized in that the layers D and E are made of a polyolefin material.
    [0010]
    10. multilayer film according to one of claims 1 to 9, characterized in that the thickness of the layer A varies from 8 to 25 i.tm, and the thickness of the bonding layers B and C is between 1 and 10 i.tm.
    [0011]
    11. multilayer film according to one of claims 1 to 10, characterized in that the thickness of the layer A varies from 10 to 20 i.tm, and the thickness of the bonding layers B and C is between 2 and 8 i.tm.
    [0012]
    12. Multilayer film according to one of claims 1 to 11, characterized in that it is a 5-layer film consisting of the adhesive layer A, the 2 intermediate layers B and C and the two outer layers D and E, according to the sequence D / B / A / C / E in which the sign "/" means that the faces of the layers concerned are in direct contact.
    [0013]
    13. A method of manufacturing the multilayer film as defined in one of claims 1 to 12, characterized in that it comprises the co-extrusion of the self-adhesive hot melt composition, compositions b and c, and materials constituent of layers D and E.
    [0014]
    14. A method of manufacturing the multilayer film according to claim 13, characterized in that the coextrusion is carried out by blowing bubble.
    [0015]
    15. Use of the multilayer film as defined in one of claims 1 to 12 for the manufacture of reclosable packages.
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    同族专利:
    公开号 | 公开日
    US10000043B2|2018-06-19|
    IL238936A|2018-11-29|
    MX2015006479A|2016-01-11|
    AU2015202759B2|2018-11-15|
    PL2946920T3|2017-09-29|
    EP2946920A1|2015-11-25|
    AU2015202759A1|2015-12-10|
    CN105082692A|2015-11-25|
    JP2016005903A|2016-01-14|
    KR102303058B1|2021-09-15|
    DK2946920T3|2017-04-03|
    KR20150135117A|2015-12-02|
    EP2946920B1|2017-03-01|
    CN105082692B|2020-06-16|
    ES2621111T3|2017-07-03|
    BR102015011912B1|2021-09-08|
    FR3021250B1|2016-07-01|
    JP6660676B2|2020-03-11|
    US20150336362A1|2015-11-26|
    LT2946920T|2017-06-26|
    BR102015011912A2|2018-01-02|
    CA2891167A1|2015-11-22|
    引用文献:
    公开号 | 申请日 | 公开日 | 申请人 | 专利标题
    US20070092748A1|2005-09-13|2007-04-26|Asahi Kasei Life & Living Corporation|Multilayer film for top-seal|
    WO2012045951A1|2010-09-27|2012-04-12|Bostik S.A.|Multilayer film for resealable packaging|
    EP2687362A1|2012-07-19|2014-01-22|Bostik Sa|Multilayer film for flexible package|
    FR2793777B1|1999-05-21|2001-06-22|Soplaril Sa|RECLOSABLE PACKAGE WITH CONTAINER COMPRISING A TEARABLE WELDING LAYER, MANUFACTURING METHOD THEREOF|
    FR2820751B1|2001-02-09|2005-01-14|Bostik Findley|HOT EXTRUDABLE SELF-ADHESIVE THERMOFUSIBLE ADHESIVES AND THEIR USE IN MULTILAYER FILMS|
    US20050100695A1|2003-11-12|2005-05-12|Holbert Victor P.|Low surface energy blends useful in the manufacture of ovenable containers|
    FR2965272B1|2010-09-27|2014-07-11|Bostik Sa|NEW EXTRUDABLE THERMOFUSIBLE SELF-ADHESIVES FOR MULTILAYER FILMS|
    ES2864849T3|2011-07-27|2021-10-14|Performance Mat Na Inc|Multilayer films for reclosable packaging|
    FR2993897B1|2012-07-30|2015-08-21|Bostik Sa|SELF-ADHESIVE SELF-ADHESIVE FOR REFERMABLE PACKAGING WITH IMPROVED ORGANOLEPTIC PROPERTIES|FR3023560B1|2014-07-08|2016-08-05|Bostik Sa|EXTRUDABLE THERMOFUSIBLE SELF-ADHESIVES FOR REFERMABLE PACKAGING WITH IMPROVED ORGANOLEPTIC PROPERTIES|
    FR3075092B1|2017-12-19|2019-12-27|Bostik Sa|MULTILAYER FILM INCLUDING A FLUORINATED POLYMER AND ITS USE FOR A RECLOSABLE PACKAGE|
    FR3075091B1|2017-12-19|2019-12-27|Bostik Sa|MULTILAYER FILM INCLUDING A NON-IONIC SURFACTANT AND ITS USE FOR A RECLOSABLE PACKAGE|
    JP2019130471A|2018-01-31|2019-08-08|東洋アルミエコープロダクツ株式会社|Electrostatic filter structure|
    KR101921958B1|2018-04-03|2018-11-27|진영산업 |Transparent roll film easily detachable to an open packing box and manufacturing method thereof|
    FR3088239B1|2018-11-08|2020-11-20|Bostik Sa|NEW MULTI-LAYER FILM FOR ENHANCED CLOSURE RESEALABLE PACKAGING|
    CN109605886A|2018-11-15|2019-04-12|永新股份（黄山）包装有限公司|A kind of high-temperature resistant nano grade tack optical protection layer and its production method|
    法律状态:
    2015-05-08| PLFP| Fee payment|Year of fee payment: 2 |
    2015-11-27| PLSC| Publication of the preliminary search report|Effective date: 20151127 |
    2016-04-12| PLFP| Fee payment|Year of fee payment: 3 |
    2017-04-13| PLFP| Fee payment|Year of fee payment: 4 |
    优先权:
    申请号 | 申请日 | 专利标题
    FR1454597A|FR3021250B1|2014-05-22|2014-05-22|MULTILAYER FILM FOR REFERMABLE PACKAGING WITH ENHANCED REFINERY|FR1454597A| FR3021250B1|2014-05-22|2014-05-22|MULTILAYER FILM FOR REFERMABLE PACKAGING WITH ENHANCED REFINERY|
    CA2891167A| CA2891167A1|2014-05-22|2015-05-12|Multilayer film for resealable packaging with improved resealing|
    EP15167928.9A| EP2946920B1|2014-05-22|2015-05-18|Multilayer film for reclosable packaging with improved reclosing|
    ES15167928.9T| ES2621111T3|2014-05-22|2015-05-18|Multilayer film for reclosable container with improved reclosing system|
    DK15167928.9T| DK2946920T3|2014-05-22|2015-05-18|MULTI-LAYER MOVIE PACKAGING WITH IMPROVED CLOSING|
    LTEP15167928.9T| LT2946920T|2014-05-22|2015-05-18|Multilayer film for reclosable packaging with improved reclosing|
    PL15167928T| PL2946920T3|2014-05-22|2015-05-18|Multilayer film for reclosable packaging with improved reclosing|
    KR1020150070388A| KR102303058B1|2014-05-22|2015-05-20|Multilayer film for resealable packaging having improved resealing|
    US14/718,215| US10000043B2|2014-05-22|2015-05-21|Multilayer film for resealable packaging having improved resealing|
    IL238936A| IL238936A|2014-05-22|2015-05-21|Moltilayer film for resealable packaging having improved resealing|
    AU2015202759A| AU2015202759B2|2014-05-22|2015-05-21|Multilayer film for resealable packaging having improved resealing|
    BR102015011912-7A| BR102015011912B1|2014-05-22|2015-05-22|MULTI-LAYER FILM, PROCESS FOR MANUFACTURING MULTI-LAYER FILM AND USE OF MULTI-LAYER FILM|
    CN201510264859.8A| CN105082692B|2014-05-22|2015-05-22|Multilayer film for resealable packaging with improved resealing|
    JP2015104086A| JP6660676B2|2014-05-22|2015-05-22|Resealable multi-layer packaging film with improved resealability|
    MX2015006479A| MX2015006479A|2014-05-22|2015-05-22|Multilayer film for resealable packaging having improved resealing.|
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