• 专利附录
  • 专利说明
  • 权利要求
  • 类似技术
  • 同族专利
  • 引用文献
  • 法律状态
  • 优先权
    • 专利摘要:
    1) Hot melt self-adhesive composition with MFI of 0.01 to 200 g / 10 minutes and comprising: - from 45 to 70% by weight of a composition of styrenic block copolymers of SIS type with a diblock content of from 30 to 90 % and content of styrenic units of 10 to 40%; and from 30 to 55% by weight of at least one tackifying resin having a softening temperature of between 5 and 150 ° C. and obtained by a process comprising: a first polymerization step of a composition chosen from: composition (i) consisting essentially of unsaturated hydrocarbons having 9 carbon atoms, or - a composition (ii) consisting essentially of dicyclopentadiene and its derivatives having 10 carbon atoms; then - a second hydrogenation step of the polymer thus obtained. 2) multilayer film comprising an adhesive layer consisting of said composition with a thickness of between 7 and 50 microns. 3) A method of manufacturing said film by coextrusion. 4) Use of said film for the manufacture of resealable trays
    公开号:FR3023560A1
    申请号:FR1456561
    申请日:2014-07-08
    公开日:2016-01-15
    发明作者:Christophe Robert
    申请人:Bostik SA；
    IPC主号:
    专利说明:

    [0001] The present invention relates to a novel extrudable hot-melt self-adhesive composition, and to a multilayer film for the manufacture of resealable packages (or trays), which comprises a diapered layer. The present invention relates to a novel self-adhesive hot-melt extrudable composition. adhesive constituted by said composition and which has improved organoleptic properties.
    [0002] Applications include WO 02/064694, WO 12/045950 and WO 12/045951 extrudable hot melt self-adhesive compositions for use in the manufacture of resealable packaging (or trays). The reclosable trays are used in the food industry and retail for the packaging of foodstuffs, especially fresh products. Such packages are described by US Pat. No. 4,673,601 and patent application EP 1053952. After a first opening of the packaging and consumption of a portion of the food product that it contains, the user can manually close the packaging so that substantially hermetic and therefore ensure, if appropriate after refrigeration, the preservation of 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, flat cover, which consists of a multilayer film (also called composite or composite) generally of thickness between 40 and 150 μm, and which is sometimes referred to as the lidding film denomination. 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, optionally, 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").
    [0003] 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. 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 self-adhesive hot-melt compositions, which are prepared by hot mixing of their ingredients, have the additional advantage of being able to be put into the form of granules (between 1 and 10 mm in size) by means of an extrusion step performed directly hot after the mixing step, for example by means of a twin screw extruder provided with a cutting tool of the extruded product. Thanks to the granules thus obtained, the film, for example 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, in particular by feeding sheath blowing device by the constituent materials of the 3 layers in the form of granules of previously defined size. However, in the context of the constant improvement of the food packaging proposed by the industry to the consumer, it now appears more and more necessary to consider the impact of said packaging on a possible alteration of the organoleptic properties of foodstuffs. packaged, and in particular on a risk of alteration of their taste and / or their smell (or perfume), especially in the case of hermetic packaging. As regards the self-adhesive hot melt compositions for reclosable packages known from the prior art, it is considered that this impact can result from the presence in said compositions of very small quantities - up to a maximum limit of 5 ppm of compounds. volatile organic compounds of low molecular weight (less than 1000 Da) originating from the impurities present in the raw materials: for example residues of the monomers or oligomers which are used in the polymerization reactions of styrenic block copolymers or tackifying resins. It is thus impossible to avoid the risk that, in the final packaging, volatile organic compounds present in trace amounts in the hot-melt self-adhesive composition migrate through the layers of thermoplastic materials of the complex film to penetrate the foodstuff. food, and modify its organoleptic properties. This risk is even less likely to be discounted if we consider that some people who are very sensitive to olfactory and / or taste sensations are able to detect traces up to 1 ppb of certain substances. The patent application WO 14/020243 describes, for this same organoleptic problem, a hot-melt self-adhesive composition which is constitutive of a binder layer, in a multilayer film, 2 thin layers of thermoplastic material, and which necessarily comprises a hydrophobic zeolite . The purpose of the present invention is to propose another extrudable hot-melt self-adhesive composition than that described by the latter application, which makes it possible, without requiring the presence of a hydrophobic zeolite, to confer on the multilayer film of which it constitutes the adhesive layer. , a lower risk of altering the organoleptic properties of the packaged foodstuff, and more particularly its taste. Another object of the present invention is to provide an extrudable hot-melt self-adhesive composition having improved appearance homogeneity, including in the adhesive layer included in the multilayer film.
    [0004] Another object of the present invention is to provide an extrudable hot melt self-adhesive composition and a multilayer film which comprises two thin layers of thermoplastic materials bonded together by a layer of said composition, and which provides these two thin layers with opening and closing properties, suitable for the use of said film for the manufacture of a resealable package.
    [0005] Another object of the present invention is to manufacture said multilayer film by an industrial method of hot coextrusion of the materials constituting each layer, such as coextrusion by blow-molding, comprising the introduction of said materials in the form of of granules.
    [0006] The present invention therefore relates firstly to a hot-melt self-adhesive composition having a flow index (or MFI) ranging from 0.01 to 200 g / 10 minutes and comprising, on the basis of the total weight of said composition a: - from 45 to 70% by 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 Styrene-Isoprene diblock copolymer (SI), and from 10 to 70% by weight of at least one linear triblock copolymer StyreneIsoprene-Styrene (SIS); 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 55% by weight of at least one tackifying resin a2 having a softening temperature of between 5 and 150 ° C. and obtained by a process comprising: a first polymerization step of a composition chosen from: a composition (i) consisting essentially of unsaturated hydrocarbons having 9 carbon atoms, or - a composition (ii) consisting essentially of dicyclopentadiene and its derivatives having 10 carbon atoms; then - a second hydrogenation step of the polymer thus obtained.
    [0007] It has indeed been found that the choice of the specific tackifying resin a2 combined with the choice of a styrenic block copolymer of the SIS / SI type makes it possible, surprisingly, to obtain a multilayer film which is suitable for the manufacture of packaging. reclosable for foodstuffs, and which also makes it possible to lower the risk of altering the organoleptic properties of the packaged foodstuffs. In addition, the hot-melt self-adhesive composition according to the invention is extrudable, which makes it possible to present it in the form of granules having a size of between 1 and 10 mm, which is particularly advantageous for the manufacture of the corresponding multilayer film. The above percentages as well as those used generally in the present text for expressing quantities correspond, in the absence of any indication to the contrary, to weight / weight percentages. It is also specified that the percentages indicated above for the contents, in composition a, of the composition α of block copolymers and of the tackifying resin α 2 are percentages relative to the total weight of said composition a. It is the same for the percentages indicated for the optional components included in the composition which are specified later in the present text. The copolymers SI and SIS included in the composition according to the invention have a weight average molecular weight M of between 60 kDa and 400 kDa. In the absence of any indication to the contrary, the weight average molar masses M, which are given in the present text, are expressed in dalton (Da) and are determined by Gel Permeation Chromatography, the column being calibrated with polystyrene standards. . According to a preferred variant of the self-adhesive hot-melt composition a according to the invention, the diblock content SI in the composition al of styrenic block copolymers can vary from 50 to 80%, more preferably from 55 to 80%. According to yet another preferred variant, the total styrenic unit content of the al composition of styrenic block copolymers can vary from 13 to 18%. The SIS and SI type copolymers which may be used for the preparation of the hot-melt adhesive self-adhesive composition are commercially available. Said copolymers are themselves available in the form of triblock / diblock compositions. Kraton® D1113BT from Kraton and Quintac® 3520 from Zeon Chemicals are examples of such compositions. Kraton® D1113BT is a composition having a total styrenic unit content of 16%, consisting of 45% linear SIS triblock copolymer of about 250 kDa, and 55% diblock copolymer SI of 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 hot-melt self-adhesive composition according to the invention comprises at least one (or more) tackifying resin a2. This resin a2 has a weight average molecular weight M, generally between 300 and 5000 Da. The softening temperature (or point) of the tackifying resins used in the composition a may vary from 5 to 150 ° C. The softening temperature (commonly referred to in the art as "R & B" for "Ring and Ball") 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. A softening temperature of 80 to 150 ° C is more particularly preferred. The process for obtaining the resin a2 is carried out, in a first step, by polymerization of the constituent compounds of the compositions (i) or (ii), which are for example obtained from the distillation of the naphtha. The unsaturated hydrocarbons of the composition (i) may be aliphatic or not. The hydrogenation of the polymer obtained is carried out according to known methods, leading to a partial or total hydrogenation of the unsaturated bonds, preferably total.
    [0008] Many resins meeting the definition of a2 resin are commercially available. Examples of such resins are: Regalite TM R1125, available from Eastman, which is a fully hydrogenated resin having a softening temperature of 125 ° C., a weight average molar mass Mw of 1200 Da, and is obtained by polymerization of a composition (i) of unsaturated hydrocarbons having 9 carbon atoms; Escorez ™ 5340, available from Exxon Mobil, which is a totally hydrogenated resin having a softening temperature of 140 ° C., a weight average molecular weight M w of 680 Da, and which is obtained by polymerization of a composition ; Escorez TM 5400, available from Exxon Mobil, which is a partially hydrogenated resin having a softening temperature of 100 ° C., a weight average molecular weight M w of 570 Da, and which is obtained by polymerization of a composition (ii) Other examples of commercially available a2 resins are Eastman RegaliteTM R1090 and R1100 (R & B of 90 ° C and 100 ° C respectively), ArkonTM P90, P100, P125 available from Arakawa (R & B). respective 90 ° C, 100 ° C and 125 ° C), EscorezTM 5300 and 5380 ExxonMobil company (respectively R & B 105 ° C and 85 ° C, and M, respectively 590 and 460 Da), SukorezTM SU90 SU100, SU 120 from Kolon (respective R & B of 90 ° C, 100 ° C, 120 ° C).
    [0009] According to a preferred variant, the hot-melt self-adhesive composition according to the invention comprises from 50 to 70% of the composition a and from 30 to 50% of the (or more) tackifying resin a2. According to another preferred variant, the composition a consists essentially of the composition a1 and the tackifying resin a2 in amounts within the ranges specified above. The term "essentially constituted" is intended to mean that, in addition to the composition a1 and the tackifying resin (s) a2, the composition also contains one or more optional components, but in a quantity not exceeding 5%, and Preferably 2%. Such optional components, whose content in the composition can range from 0.1 to 2% are for example stabilizers (or antioxidants). 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 resins. tackifying. These compounds may include primary antioxidants that trap free radicals and are generally substituted phenols such as Irganox® 1010 from CIBA. The primary antioxidants can be used alone or in combination with other antioxidants such as phosphites, such as IgaAs also from CIBA, or with UV stabilizers such as amines. Another example of such optional components is a plasticizer whose content in the composition does not exceed 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. Finally, other examples of such optional components are mineral or organic fillers, pigments or dyes. The Melt Flow Index (MII) of the self-adhesive hot-melt composition a is measured at 190 ° C. and for a total weight of 2.16 kg, in accordance with the condition d) of the ISO 1133 standard. The MIT is the composition mass (previously placed in a vertical cylinder) which flows in 10 minutes through a fixed diameter die, under the effect of a pressure exerted by a loaded piston having the total weight 2.16 kg. In the absence of mention to the contrary, the MFI values given in this text have been measured under the same conditions. Hot melt self-adhesive compositions having an MFI ranging from 2 to 70 g / 10 minutes are more particularly preferred.
    [0010] According to a very particularly preferred variant for producing the multilayer film, the composition according to the invention is in the form of granules with a size of between 1 and 10 mm, preferably between 2 and 5 mm. The composition may be prepared in this form by a process which comprises: - a simple step of mixing the ingredients 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, then - a cooling step, for example at room temperature. The subject of the present invention is secondly a multilayer film comprising two thin layers B and C of thermoplastic material bonded together by an adhesive layer A, characterized in that said layer A has a thickness of between 7 and 50 μm and is constituted by the self-adhesive hot-melt composition a as defined above. The adhesive layer A preferably provides the connection between a complexable thin film B and a sealable and breakable thin film C.
    [0011] The thickness of the adhesive layer A is preferably between 7 and 35 μm, and even more preferably between 7 and 25 μm. According to another preferred variant, the thickness of the layer A may also be between 10 and 35 μm, or better still between 10 and 25 μm. The complexable layer B may be complexed (or laminated) with other layers for producing the package, for example with a rigid layer for producing the receptacle. The sealable and breakable layer C ensures, at 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 mother adhesive layer and located on the cap strip and / or the receptacle strip. The material used to form the two layers B and C 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). It is preferred to use to form the two layers B and C a polyolefinic material, and especially PE, and even more preferably a low density PE (also referred to as Low Density PolyEthylene or LDPE). The thickness of layers B and C is likely to vary over a wide range from 5 to 150 μm. According to a preferred variant, the multilayer film according to the invention comprises, in addition to the layers A, B and C, 2 bonding layers D and E such that the adhesive layer A is: - connected to the layer B via the layer D, and - connected to the layer C via the layer E. The link layers D and E are also designated by the term "intermediate layers" or by the term "tie layers" and generally have a thickness of between 1 and 10 μm, preferably between 2 and 8 μm. The use of such bonding layers advantageously makes it possible to improve the quality of the reclosure of the multilayer film, and therefore of the corresponding reclosable packaging, thus ensuring the consumer more effectively the preservation of the remaining portion of the perishable food product. contained in the package, after the first opening of the package. The linking layers D and E respectively consist of compositions d and e, identical or different, having a melting temperature of about 80 to 120 ° C and essentially comprising polymers chosen from: homopolymers or copolymers of ethylene homopolymers or copolymers of propylene, copolymers of ethylene with a polar comonomer, and homopolymers or copolymers of grafted polyolefins.
    [0012] Reference is made for further details on these compositions d and e to US2013 / 0029553. Preferably, compositions d and e each comprise 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.
    [0013] According to another variant embodiment, the multilayer film according to the invention comprises, in addition to the 3 essential layers A, B and C, and the two optional layers D and E, other thin layers necessary for producing the package, as for example: - a 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 B and C.
    [0014] According to an alternative embodiment, the multilayer film according to the invention is a 3-layer film constituted by the adhesive layer A and the two layers B and C, according to the sequence B / A / C / in which the sign "/" means that the faces of the layers concerned are in direct contact. According to another variant embodiment, the multilayer film according to the invention is a film with 5 layers constituted by the adhesive layer A, the two intermediate layers D and E and the two outer layers B and C, according to the sequence B / D / A / E / C in which the sign "/" signifies that the faces of the layers concerned are in direct contact. The present invention also relates to a method of manufacturing the multilayer film as defined above, characterized in that it comprises a step of coextrusion of the self-adhesive hot melt composition a and materials constituting layers B and C and, the where appropriate, layers D and E. Preferably, the compositions and materials constituting the layers A, B, C and, if appropriate, D and E are fed into the coextrusion device in the form of granules of size 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 aforementioned granules. 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 (as for example for the connecting layers D and E), either by a laminating process directly from the coextrusion film, using for example a polyurethane adhesive. The coextrusion device used in the manufacturing process is preferably a bubble blow coextrusion device (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 and C, as well as, if appropriate, D and E, and then passing corresponding flows through a set of annular and concentric dies, so as to form a multi-layer tubular bubble, in the order corresponding to that desired for the final structure, and then - the radial expansion (relative to the annular die ) and the stretching (in the axial direction) of the bubble, then - the 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. 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.
    [0015] Example A (reference): 1. Preparation of a hot-melt self-adhesive composition a: The adhesive composition indicated in the following Table is prepared in the form of granules with a size of about 4 mm, by mixing its ingredients at 160.degree. using a 2-screw extruder, extrusion through a die, then cutting the extruded product and cooling to room temperature. The measured MIT is 57 g / 10 minutes. 2. Preparation of a B / A / C Three-Layer Film Comprising a Layer A of the Composition of Example A: This three-layer film is produced by means of a pilot device for continuous bubble-blowing coextrusion, in which 3 extruders are fed: - for one, by the composition a of example A, and - for the 2 others, by LDPE; the 3 compositions being in the form of granules with a size of about 4 mm. The process parameters are adjusted so as to produce a three-layer film consisting of: as layer A, a layer of thickness 15 μm made of the composition of example A, as a complexable thin layer D, a 30 μm thick layer made of LDPE; as a sealable and breakable thin layer E, a layer of thickness 15 iam also made of LDPE.
    [0016] 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.
    [0017] 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 thickness 23 i.tm using a solvent-based adhesive based on polyurethane and using a Mayer bar type coating apparatus. 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.
    [0018] 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.
    [0019] While a drive mechanism communicates to the moving part a uniform speed of 300 mm / minute leading to the peeling of the 2 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.
    [0020] The strength obtained is indicated in the Table. 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 return movement is made 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.
    [0021] The strength obtained is indicated in the Table. Test of evaluation of the alteration of the taste of butter put in contact with the adhesive composition: This test is carried out on a 125 g butter plate of dimensions 110 x 65 x 17 mm. This wafer is centered horizontally on a rectangle of dimensions 110 × 65 mm cut in the sheet of three-layer film in A4 format mentioned above, the wafer being in contact with the sealable and breakable layer E of said film.
    [0022] The upper face of the butter plate is then covered with a second rectangle of tricouche film identical to the first, and is also in contact with the sealable and breakable layer E. The structure thus obtained is overwrapped in aluminum foil and then placed during 10 days in a refrigerator kept at 10 ° C.
    [0023] As a control, it is also during the same time storage in the same refrigerator of a wafer of butter identical to the previous one, which is simply packaged in aluminum foil. After 10 days, the 2 platelets of butter are recovered, each cut into 20 pieces of about 6 g and sent to a panel of 10 people for taste assessment. Each member of the panel attributes, after tasting, a score of 0 to 4 to the pieces from the wafer placed in contact with the three-layer film comprising the adhesive layer A, with respect to the pieces from the control wafer, according to the following scale: 0 = no noticeable difference 1 = barely noticeable difference 2 = small difference 3 = marked difference 4 = large difference. The average score obtained is shown in the Table.
    [0024] Examples 1 and 2 (according to the invention): Example A is repeated with the compositions indicated in the Table. The MIT obtained for each composition a, the forces measured for the 1st and 2nd openings are indicated in the Table, as well as the results of the evaluation test of the alteration of the taste of the butter.
    [0025] It is observed that the force of first opening remains substantially stable with respect to that measured for the reference example A. On the other hand the force of 2nd opening is lowered, but is estimated to correspond to a quality of reclosure (following the first opening of the package), still acceptable.
    [0026] On the other hand, the alteration of the taste of the butter resulting from the composition a is very significantly reduced compared with Example A.
    [0027] Table Ingredient% w / w% Example A (ref.) Example 1 Example 2 Kraton® Composition D1113BT 59.7 39.8 39.8 Quintac® 3520 - 19.9 19.9 Escorez® 1310LC 24.9 - - Regalite® R1125 - 39.8 - Escorez® 5340 - - 39.8 Dercolytee S115 14.9 - - Irganox® 1010 0.5 0.5 0.5 Design content Styrenic al compounds (in% 16 16 16 w / weight) Content in diblocks 56 63 63 (% w / w) MFI composition (in g / 10 min) 57 56 56 Thinning film Force of the 1st opening 3 2.8 3.1 (in N / cm) Strength of 2 '' '' aperture 0.84 0.5 0.6 (in N / cm) Altered taste of butter 0.4 0.2 0.1
    权利要求:
    Claims (16)
    [0001]
    REVENDICATIONS1. A hot-melt self-adhesive composition having a flow index of from 0.01 to 200 g / 10 minutes and comprising, based on the total weight of said composition: from 45 to 70% by weight of a composition 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 Styrene-Isoprene diblock copolymer (SI), and from 10 to 70% by weight of at least one linear triblock copolymer Styrene Isoprene-Styrene (SIS); 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 55% by weight of at least one tackifying resin a2 having a softening temperature of between 5 and 150 ° C. and obtained by a process comprising: a first polymerization step of a composition chosen from: a composition (i) consisting essentially of unsaturated hydrocarbons having 9 carbon atoms, or - a composition (ii) consisting essentially of dicyclopentadiene and its derivatives having 10 carbon atoms; then - a second hydrogenation step of the polymer thus obtained. 25
    [0002]
    2. hot-melt self-adhesive composition according to claim 1, characterized in that the content of diblocs SI in the composition al varies from 50 to 80 ° A.
    [0003]
    3. Self-adhesive hot melt composition according to one of claims 1 or 2, characterized in that the softening temperature of the tackifying resin a2 is between 80 and 150 ° C.
    [0004]
    4. Self-adhesive hot melt composition according to one of claims 1 to 3, characterized in that it consists essentially of the composition al and a tackifying resin a2.
    [0005]
    5. hot-melt self-adhesive composition according to one of claims 1 to 4, characterized in that its flow index is from 2 to 70 g / 10 minutes.
    [0006]
    6. hot-melt self-adhesive composition according to one of claims 1 to 5, characterized in that it is in the form of granules of size between 1 and 10 mm.
    [0007]
    7. Multilayer film comprising two thin layers B and C of thermoplastic material bonded together by an adhesive layer A, characterized in that said layer A has a thickness of between 7 and 50 nm and is constituted by the self-adhesive hot-melt composition as defined in one of claims 1 to 6.
    [0008]
    8. Multilayer film according to claim 7, characterized in that the thickness of the adhesive layer A is between 7 and 35 nm. 20
    [0009]
    9. Multilayer film according to one of claims 7 or 8, characterized in that it comprises, in addition to the layers A, B and C, 2 bonding layers D and E such that the adhesive layer A is: - connected to the layer B via the D layer, and - connected to the layer C via the E layer.
    [0010]
    10. multilayer film according to one of claims 7 to 9, characterized in that the bonding layers D and E consist of compositions d and e, identical or different, having a melting temperature of about 80 to 120 ° C and essentially comprising polymers selected from: homopolymers or copolymers of ethylene, homopolymers or copolymers of propylene, copolymers of ethylene with a polar comonomer, and homopolymers or copolymers of grafted polyolefins.
    [0011]
    11. Three-layer film according to one of claims 7 or 8, characterized in that it consists of the adhesive layer A and the two layers B and C, according to the sequence B / A / C / wherein the sign " / "Means that the faces of the layers concerned are in direct contact.
    [0012]
    12. 5-layer film according to one of claims 9 or 10, characterized in that it consists of the adhesive layer A, the two intermediate layers D and E and the two outer layers B and C, according to the sequence B / D / A / E / C 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 7 to 12, characterized in that it comprises a step of co-extrusion of the self-adhesive hot melt composition a and materials constituting layers B and C and, if appropriate, layers D and E.
    [0014]
    14. The manufacturing method according to claim 13, characterized in that the compositions and materials constituting the layers A, B, C and, where appropriate, D and E are fed into the coextrusion device in the form of granules of size between 1 and 10 mm.
    [0015]
    15. A method of manufacturing the multilayer film according to one of claims 13 or 14, characterized in that the coextrusion device used is a coextrusion device bubble blowing.
    [0016]
    16. Use of the multilayer film as defined in one of claims 7 to 12 for the manufacture of resealable packages.
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    同族专利:
    公开号 | 公开日
    ES2627991T3|2017-08-01|
    US20200377771A1|2020-12-03|
    AU2015203789A1|2016-01-21|
    AU2015203789B2|2018-12-13|
    IL239626A|2019-11-28|
    EP2966140B1|2017-05-10|
    CN105255413B|2020-11-03|
    JP2016017180A|2016-02-01|
    US10787595B2|2020-09-29|
    US20160009965A1|2016-01-14|
    JP6814530B2|2021-01-20|
    KR20160006121A|2016-01-18|
    BR102015016470A2|2017-05-02|
    CA2895727A1|2016-01-08|
    FR3023560B1|2016-08-05|
    CN105255413A|2016-01-20|
    MX2015008832A|2016-02-09|
    EP2966140A1|2016-01-13|
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    法律状态:
    2015-06-29| PLFP| Fee payment|Year of fee payment: 2 |
    2016-01-15| PLSC| Search report ready|Effective date: 20160115 |
    2016-06-13| PLFP| Fee payment|Year of fee payment: 3 |
    2017-06-13| PLFP| Fee payment|Year of fee payment: 4 |
    2018-06-12| PLFP| Fee payment|Year of fee payment: 5 |
    2019-06-19| PLFP| Fee payment|Year of fee payment: 6 |
    2020-02-28| CA| Change of address|Effective date: 20200122 |
    2020-06-12| PLFP| Fee payment|Year of fee payment: 7 |
    2021-06-11| PLFP| Fee payment|Year of fee payment: 8 |
    优先权:
    申请号 | 申请日 | 专利标题
    FR1456561A|FR3023560B1|2014-07-08|2014-07-08|EXTRUDABLE THERMOFUSIBLE SELF-ADHESIVES FOR REFERMABLE PACKAGING WITH IMPROVED ORGANOLEPTIC PROPERTIES|FR1456561A| FR3023560B1|2014-07-08|2014-07-08|EXTRUDABLE THERMOFUSIBLE SELF-ADHESIVES FOR REFERMABLE PACKAGING WITH IMPROVED ORGANOLEPTIC PROPERTIES|
    IL23962615A| IL239626A|2014-07-08|2015-06-25|Extrudable hot-melt pressure-sensitive adhesives for resealable packaging having improved organoleptic properties|
    CA2895727A| CA2895727A1|2014-07-08|2015-06-25|Fusible extrudable self-adhesives for resealable packaging with improved organoleptic properties|
    ES15174317.6T| ES2627991T3|2014-07-08|2015-06-29|Self-adhesive extrudable hot melt adhesives for resealable containers, with improved organoleptic properties|
    EP15174317.6A| EP2966140B1|2014-07-08|2015-06-29|Extrudable hot-melt pressure-sensitive adhesives for resealable packaging having improved organoleptic properties|
    JP2015132447A| JP6814530B2|2014-07-08|2015-07-01|Extrudable hot-melt pressure-sensitive adhesive for resealed packaging with improved sensory irritation|
    US14/792,973| US10787595B2|2014-07-08|2015-07-07|Extrudable hot-melt pressure-sensitive adhesives for resealable packaging having improved organoleptic properties|
    AU2015203789A| AU2015203789B2|2014-07-08|2015-07-07|Extrudable hot-melt pressure-sensitive adhesives for resealable packaging having improved organoleptic properties|
    KR1020150096490A| KR20160006121A|2014-07-08|2015-07-07|Extrudable hot-melt pressure-sensitive adhesives for resealable packaging having improved organoleptic properties|
    BR102015016470A| BR102015016470A2|2014-07-08|2015-07-08|extrudable pressure sensitive hot melt adhesives for resealable packaging having enhanced organoleptic properties|
    CN201510397098.3A| CN105255413B|2014-07-08|2015-07-08|Extrudable hot melt pressure sensitive adhesive for resealable packaging|
    MX2015008832A| MX2015008832A|2014-07-08|2015-07-08|Extrudable hot-melt pressure-sensitive adhesives for resealable packaging having improved organoleptic properties.|
    US16/995,266| US20200377771A1|2014-07-08|2020-08-17|Extrudable hot-melt pressure-sensitive adhesives for resealable packaging having improved organoleptic properties|
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