AU2010332945B2

AU2010332945B2 - Cold sealed recloseable packaging and composition for the production thereof

Info

Publication number: AU2010332945B2
Application number: AU2010332945A
Authority: AU
Inventors: Cornelis Petrus Beyers; Florian Busch; Karl-Heinz Schumacher; Dieter Urban
Original assignee: BASF SE
Current assignee: BASF SE
Priority date: 2009-12-18
Filing date: 2010-12-15
Publication date: 2013-08-15
Anticipated expiration: 2030-12-15
Also published as: WO2011073221A2; EP2445943A2; BR112012014672A2; JP5755241B2; CN102712723A; EP2445943B1; CN102712723B; AU2010332945A1; WO2011073221A3; JP2013514403A; ES2424004T3

Abstract

The invention relates to a recloseable packaging having a cold sealed adhesive layer that can be reclosed after the packaging is opened, wherein the adhesive layer comprises a polymer in emulsion made of at least 60 wt% of main monomers selected from the group made up of C1 to C20-alkyl(meth)acrylates, vinyl esters of up to 20 C atoms comprising carbolic acids, vinyl aromates having up to 20 C atoms, ethylene unsaturated nitriles, vinyl halogenides, vinyl ethers of alcohols comprising 1 to 10 C atoms, aliphatic hydrocarbons having 2 to 8 C atoms and one or two double bonds, and mixtures of said monomers, wherein the polymer in emulsion can be produced by means of emulsion polymerization of radically polymerizable monomers in the presence of at least one protective colloid. The invention further relates to aqueous polymer dispersions suitable for producing the packaging according to the invention, and to polymer films coated with the polymer dispersion.

Description

1 Cold sealed recloseable packaging and composition for the production thereof The invention relates to a recloseable pack having a cold-sealed layer of adhesive which is recloseable after the pack has been opened, to a method for producing the 5 pack, to a composition in the form of an aqueous polymer dispersion for producing the pack, and to a polymer film coated with the composition. Cold-sealable compositions are bonding compositions which, following application to and drying on a substrate, are not tacky to the touch, yet bond to one another when 10 pressed against one another at room temperature with pressure. They differ from pressure-sensitive adhesives in the absence of, or only very low, tack at room temperature. They differ from heat-sealable compositions in that they can be adhered to one another under pressure without heat activation. Known applications of cold sealable compositions include, for example, the closing of pouchlike packs, more 15 particularly for foods or other heat-sensitive products in whose packaging the use of heat is undesirable, such as ice cream or chocolate, for example, or when fast packing speeds and high cycle rates are required. On account of their nontacky properties, substrates coated with them can be rolled up into rolls and stored prior to use, without adhesion to the opposite, other side of the carrier substrate, said other side being 20 provided preferably with a release coating. Typically, for cold-seal adhesives, polymer dispersions based on natural rubber latex are used. Disadvantages associated with natural rubber latex include a comparatively high price volatility, natural fluctuations in the quality of the natural raw material, and, in particular, the allergenic potential harbored by these natural products. There is a desire for cold-sealable compositions 25 which as far as possible are free from organic solvents, i.e., for aqueous dispersions of polymers which, after drying, form a cold-sealable coating. For multiple recloseability of a pack it is important that the closure forces are still sufficiently high even after repeated opening. Polymer dispersions based on natural 30 rubber or based on synthetic polymers frequently do not combine all of the properties desired for the production of recloseable packs, in terms of sufficiently high sealed seam strength on initial closing, blocking resistance with respect to a release coating, and sufficiently high reclosure forces following repeated opening and reclosing of a pack. 35 EP 1939106 A describes cold-sealed, recloseable packs. With the natural lattices and synthetic polymers stated therein, such as acrylate polymers and acrylate/styrene copolymers, for example, it is not readily possible to attain the desired values for the initial opening forces and for the reclosing forces. 40 It is an object of the invention to provide compositions for producing cold-sealable films, and recloseable packs producible with these films, that combine, with the maximum possible effect, a combination of positive properties with regard to cold sealability, 2 blocking resistance, and recloseability, and which, furthermore, are as far as possible free from allergenic potential and from organic solvents, and which can be applied as effectively as possible by conventional application technologies (such as printing, for example), more particularly to film substrates. 5 The object is achieved in accordance with the invention by means of a recloseable pack having a cold-sealed layer of adhesive which is recloseable after the pack has been opened, the layer of adhesive comprising an emulsion polymer composed to an extent of at least 60% by weight of principal monomers selected from the group 10 consisting of C1 to C20 alkyl (meth)acrylates, vinyl esters of carboxylic acids comprising up to 20 C atoms, vinylaromatics having up to 20 C atoms, ethylenically unsaturated nitriles, vinyl halides, vinyl ethers of alcohols comprising 1 to 10 C atoms, aliphatic hydrocarbons having 2 to 8 C atoms and one or two double bonds, and mixtures of these monomers, the emulsion polymer being preparable by emulsion 15 polymerization of free-radically polymerizable monomers in the presence of at least one protective colloid and having a glass transition temperature in the range from -30 to OC. The layer of adhesive comprising the emulsion polymer can be prepared by coating a suitable packaging substrate with a composition comprising the emulsion polymer, in the form of an aqueous polymer dispersion. 20 Cold-sealable means that, when two surfaces coated with a composition of the invention and dried are contacted with exertion of pressure at temperatures less than 400C, more particularly less than 300C or less than 250C, especially at room temperature (200C), they bond to one another. The adhesion (autoadhesion) after 25 sealing at 200C and 1.4 bar is preferably at least 2 N/15 mm, measured in accordance with the method described in the examples for determining the sealed seam strength. In practical application, cold sealing takes place advantageously at ambient temperature, in other words in general at temperatures of 10 to 300C, more particularly 15 to 250C, and under pressures of a few millibar up to several bar above atmospheric 30 pressure (1 bar), e.g., at 0.01 to 5 bar, more particularly from 0.1 to 3 bar above atmospheric pressure. The sealing time, i.e., the time during which the pressure is maintained, amounts, for example, to 0.1 to 20 seconds, more particularly 0.1 to 3 seconds, with 0.5 second being customary in particular. 35 Recloseable means that when two closure sections of a pack are contacted, after opening, at room temperature (200C) with exertion of gentle pressure, they bond to one another. The reclosure adhesion after at least five fold opening and reclosing at 200C is at least 0.5 N/15 mm, measured in accordance with the method described in the examples for determining the reclosure strength. 40 The polymer dispersions of the invention, following application to a substrate and following drying, form a coating which is preferably autoadhesive and is blocking- 3 resistant with respect to polyamide surfaces. Autoadhesive means that two coated surfaces are cold-sealable to one another. The autoadhesion of the layer of adhesive after cold sealing at 20*C and 1.4 bar is preferably at least 2 N/1 5 mm. Blocking resistant means that the adhesion of a surface coated with a composition of the 5 invention and dried, i.e., the adhesion of an unsealed layer of adhesive with respect to a polyamide surface, after loading of a circular surface with a diameter of 10 cm with 10 tonnes for one day at 200C, is not more than 0.1 N/25 mm, measured in accordance with the method described in the examples. 10 Preferred packs, coated films, and compositions have or produce an initial opening force (sealed seam strength) of at least 2 N/15 mm, a blocking resistance on the part of the cold seal coating with respect to polyamide release varnish of not more than 0.1 N/25 mm, and a reclosure strength after five fold reclosing of at least 0.5 N/15 mm, measured in each case in accordance with the methods described in the examples. 15 The polymer dispersions of the invention are dispersions of polymers in an aqueous medium. The medium in question may be, for example, fully demineralized water, or else mixtures of water and a water-miscible solvent such as methanol, ethanol or tetrahydrofuran. It is preferred not to use any organic solvents. The solids contents of 20 the dispersions are preferably from 15% to 75%, more preferably from 40% to 60%, more particularly greater than 50%, by weight. The solids content may take place, for example, by appropriately adjusting the monomer amounts and/or the amount of water used in the emulsion polymerization. The average particle size of the polymer particles dispersed in the aqueous dispersion is preferably less than 400 nm, more particularly 25 less than 300 nm. With particular preference the average particle size is between 140 and 250 nm. By average particle size here is meant the d 5 o value of the particle size distribution, i.e., 50% by weight of the total mass of all the particles have a smaller particle diameter than the d 50 figure. The particle size distribution can be determined in a known way using the analytical ultracentrifuge (W. Machtle, Makromolekulare 30 Chemie 185 (1984), pp. 1025-1039). The pH of the polymer dispersion is set preferably at a pH of more than 4, more particularly at a pH of between 5 and 9. For the inventive use, the composition may be composed solely of the water-dispersed polymer and the protective colloid. Alternatively it may also comprise further additives, 35 e.g., fillers, antiblocking agents, dyes, flow control agents, or thickeners. The polymer dispersions of the invention are preferably of low emulsifier content, which means that they comprise emulsifiers (nonpolymeric, amphiphilic, surface-active substances added to the polymerization mixture) in an amount of preferably less than 40 3% or less than 1 % by weight. Particular preference is given to emulsifier-free systems. In one embodiment of the invention, therefore, the emulsion polymerization carried out in the presence of the protective colloid takes place in emulsifier-free form, i.e., without 4 addition of emulsifiers. In the text below, the term "(meth)acryl..." and similar designations are used as an abbreviating notation for "acryl... or methacryl...". 5 Protective colloids are polymeric compounds which, on salvation, bind large quantities of water and are capable of stabilizing dispersions of water-insoluble polymers. In contrast to emulsifiers, they generally do not lower the interfacial tension between polymer particles and water. The number-average molecule weight of the protective 10 colloids is preferably above 1000 g/mol, more particularly above 2000 g/mol, and preferably up to 50 000 g/mol or up to 10 000 g/mol; for example, from 1000 to 100 000 g/mol, from 1000 to 10 000 g/mol or from 2000 to 10 000 g/mol. The protective colloids are used preferably in an amount of 0.5 to 60 parts by weight or 15 of 1 to 30 parts by weight, more preferably from 7% to 30% by weight (more particularly when the overall solids content of the composition of the invention is more than 50% by weight), based on 100 parts by weight of the monomers to be polymerized. A comprehensive description of protective colloids is given in Houben-Weyl, Methoden der organischen Chemie, Volume XIV/1, Makromolekulare Stoffe [Macromolecular 20 compounds], Georg-Thieme-Verlag, Stuttgart, 1961, pages 411 to 420. Protective colloids contemplated include, for example, amphiphilic polymers - that is, polymers having hydrophobic groups and hydrophilic groups. These may be natural polymers, such as starch, or synthetic polymers. 25 The protective colloid is preferably formed from at least 40% by weight of nonionic principal monomers, defined in more detail below, and also from a second kind of monomer, selected from ethylenically unsaturated acid monomers. The protective colloid may, furthermore, be formed optionally from additional, preferably nonionic, monomers. The protective colloid is composed preferably to an extent of at least 40%, 30 more particularly from 40% to 80% or from 50% to 80%, by weight of principal monomers selected from the group consisting of C1 to C20 alkyl (meth)acrylates, vinyl esters of carboxylic acids comprising up to 20 C atoms, vinylaromatics having up to 20 C atoms, ethylenically unsaturated nitriles, vinyl halides, vinyl ethers of alcohols comprising 1 to 10 C atoms, aliphatic hydrocarbons having 2 to 8 C atoms and one or 35 two double bonds, and mixtures of these monomers. Principal monomers for the protective colloid are, for example, (meth)acrylic acid alkyl esters with a C1-C10 alkyl radical, such as methyl methacrylate, methyl acrylate, n-butyl acrylate, ethyl acrylate, and 2-ethylhexyl acrylate. Also suitable in particular are 40 mixtures of the (meth)acrylic acid alkyl esters. Vinyl esters of carboxylic acids having 1 to 20 C atoms are, for example, vinyl laurate, vinyl stearate, vinyl propionate, Versatic acid vinyl esters, and vinyl acetate. Suitable vinylaromatic compounds include 5 vinyltoluene, alpha- and para-methylstyrene, alpha-butylstyrene, 4-n-butylstyrene, 4-n decylstyrene, and - preferably - styrene. Examples of nitriles are acrylonitrile and methacrylonitrile. The vinyl halides are ethylenically unsaturated compounds substituted by chlorine, fluorine or bromine, preferably vinyl chloride and vinylidene 5 chloride. Vinyl ethers include, for example, vinyl methyl ether or vinyl isobutyl ether. Vinyl ethers of alcohols comprising 1 to 4 C atoms are preferred. Hydrocarbons having 4 to 8 C atoms and two olefinic double bonds include butadiene, isoprene, and chloroprene. Preferred principal monomers for the protective colloid are the C1 to C 10 alkyl acrylates and methacrylates, more particularly C1 to C 8 alkyl acrylates and 10 methacrylates, and vinylaromatics, especially styrene and alpha-methylstyrene, and mixtures thereof. Very particular preference is given to methyl acrylate, methyl methacrylate, ethyl acrylate, n-butyl acrylate, n-butyl methacrylate, n-hexyl acrylate, octyl acrylate, 2-ethylhexyl acrylate, 2-propylheptyl acrylate, styrene, alpha methylstyrene, and mixtures of these monomers. 15 The protective colloid is further composed preferably to an extent of at least 15%, more particularly from 15% to 60% or from 20% to 50%, by weight of ethylenically unsaturated acid monomers. Ethylenically unsaturated acid monomers are, for example, ethylenically unsaturated carboxylic acids, ethylenically unsaturated sulfonic 20 acids, and vinylphosphonic acid. Ethylenically unsaturated carboxylic acids used are preferably alpha, beta-monoethylenically unsaturated monocarboxylic and dicarboxylic acids having 3 to 6 C atoms in the molecule. Examples thereof are acrylic acid, methacrylic acid, itaconic acid, maleic acid, fumaric acid, crotonic acid, vinylacetic acid, and vinyllactic acid. Suitable ethylenically unsaturated sulfonic acids include, for 25 example, vinylsulfonic acid, styrenesulfonic acid, acrylamidomethylpropanesulfonic acid, sulfopropyl acrylate, and sulfopropyl methacrylate. Preference is given to acrylic acid and methacrylic acid and a mixture thereof, particular preference to acrylic acid. The acid monomers can be used in the form of the free acids and also in a form partially or fully neutralized with suitable bases, for the polymerization. It is preferred to 30 use aqueous sodium or potassium hydroxide solution or ammonia as neutralizing agent. In one preferred embodiment the protective colloid (i) is used in an amount of 7% to 30% by weight, based on 100 parts by weight of the 35 monomers to be polymerized, (ii) is composed to an extent of at least 40% by weight of principal monomers selected from the group consisting of C1 to C20 alkyl (meth)acrylates, vinyl esters of carboxylic acids comprising up to 20 C atoms, vinylaromatics having up to 20 C atoms, ethylenically unsaturated nitriles, vinyl halides, vinyl ethers of alcohols 40 comprising 1 to 10 C atoms, aliphatic hydrocarbons having 2 to 8 C atoms and one or two double bonds, and mixtures of these monomers, (iii) is composed to an extent of at least 15% by weight of ethylenically unsaturated 6 acid monomers preferably selected from acrylic acid, methacrylic acid, and a mixture thereof, and (iv) has a number-average molecular weight of 1000 to 10 000. 5 The active substance that functions as binder in the layer of adhesive is the emulsion polymer preparable by emulsion polymerization of free-radically polymerizable monomers, referred to below as adhesive polymer. The adhesive polymer is composed preferably to an extent of at least 60% by weight, more preferably to an extent of at least 80% by weight, e.g., from 80% to 100% by weight, more preferably to an extent of 10 at least 90% by weight, or to an extent of 100% by weight, of one or more of the principal monomers described below. The principal monomers are selected from the group consisting of C1C20 alkyl (meth)acrylates, vinyl esters of carboxylic acids comprising up to 20 C atoms, vinylaromatics having up to 20 C atoms, ethylenically unsaturated nitriles, vinyl halides, vinyl ethers of alcohols comprising 1 to 10 C atoms, 15 aliphatic hydrocarbons having 2 to 8 C atoms and one or two double bonds, or mixtures of these monomers. Examples include (meth)acrylic acid alkyl esters with a CrC10 alkyl radical, such as methyl methacrylate, methyl acrylate, n-butyl acrylate, ethyl acrylate, and 2-ethylhexyl 20 acrylate. Also suitable in particular are mixtures of the (meth)acrylic acid alkyl esters. Vinyl esters of carboxylic acids having I to 20 C atoms are, for example, vinyl laurate, vinyl stearate, vinyl propionate, Versatic acid vinyl esters, and vinyl acetate. Suitable vinylaromatic compounds include vinyltoluene, a- and p-methylstyrene, alpha butylstyrene, 4-n-butylstyrene, 4-n-decylstyrene, and - preferably - styrene. Examples 25 of nitriles are acrylonitrile and methacrylonitrile. The vinyl halides are ethylenically unsaturated compounds substituted by chlorine, fluorine or bromine, preferably vinyl chloride and vinylidene chloride. Vinyl ethers include, for example, vinyl methyl ether or vinyl isobutyl ether. Vinyl ethers of alcohols comprising 1 to 4 C atoms are preferred. Hydrocarbons having 4 to 8 C atoms and two olefinic double bonds include butadiene, 30 isoprene, and chloroprene. Preferred principal monomers for the adhesive polymer are the C1 to C10 alkyl acrylates and methacrylates, more particularly C1 to C8 alkyl acrylates and methacrylates, and vinylaromatics, especially styrene, and mixtures thereof. Very particular preference is 35 given to methyl acrylate, methyl methacrylate, ethyl acrylate, n-butyl acrylate, n-butyl methacrylate, n-hexyl acrylate, octyl acrylate, and 2-ethylhexyl acrylate, 2-propylheptyl acrylate, styrene, and mixtures of these monomers. Besides the principal monomers, the adhesive polymer may comprise further 40 monomers, examples being monomers with carboxylic acid, sulfonic acid or phosphonic acid groups. Carboxylic acid groups are preferred. Examples include acrylic acid, methacrylic acid, itaconic acid, maleic acid or fumaric acid. Further 7 monomers are, for example, monomers also comprising hydroxyl groups, more particularly C1-Ci hydroxyalkyl (meth)acrylates, and also (meth)acrylamide. Further monomers that may be mentioned include phenyloxyethylglycol mono(meth)acrylate, glycidyl acrylate, glycidyl methacrylate, and amino (meth)acrylates such as 2 5 aminoethyl (meth)acrylate. Further monomers that may be mentioned also include crosslinking monomers. The adhesive polymer, or the emulsion polymer prepared by emulsion polymerization, is preferably free from acid groups, however. 10 More particularly the adhesive polymer is composed to an extent of at least 60% by weight, more preferably to an extent of at least 80%, e.g., from 60% to 100%, and very preferably at least 95%, or 100%, by weight of at least one C1 to C20 alkyl acrylate, at least one C1 to C20 alkyl methacrylate, a mixture thereof, or a mixture thereof with 15 styrene. In one embodiment the binder is the homopolymer of ethyl acrylate. The adhesive polymer, or the emulsion polymer prepared in the presence of at least one protective colloid, has a glass transition temperature of -30 to OC, preferably of -28 to -5 C The glass transition temperature can be determined by differential 20 scanning calorimetry (ASTM D 3418-08, midpoint temperature). The polymers can be prepared by emulsion polymerization, the product then being an emulsion polymer. The emulsion polymerization is generally carried out using ionic and/or nonionic emulsifiers and/or protective colloids or stabilizers as surface-active 25 compounds, in order to support the dispersing of the monomers in the aqueous medium. In accordance with the invention it is possible to employ one or more of the abovementioned protective colloids as sole dispersant, i.e., without the addition of emulsifiers. If desired, however, small amounts of emulsifiers can also be used as well. The emulsion polymerization preferably takes place in the presence of at least one 30 protective colloid without the addition of a nonpolymeric emulsifier. If emulsifiers are used as additional surface-active substances, they are preferably anionic or nonionic emulsifiers. Suitable emulsifiers are exemplified by ethoxylated C8 to C36 or C12 to C18 fatty alcohols having a degree of ethoxylation of 3 to 50 or of 4 to 35 30, ethoxylated mono-, di-, and tri-C 4 to C12 or C4 to CO alkylphenols having a degree of ethoxylation of 3 to 50, alkali metal salts of dialkyl esters of sulfosuccinic acid, alkali metal salts and ammonium salts of C8 to C12 alkyl sulfates, alkali metal salts and ammonium salts of C12 to C18 alkylsulfonic acids, and alkali metal salts and ammonium salts of C to C18 alkylarylsulfonic acids. Cationic emulsifiers are, for example, 40 compounds having at least one amino group or ammonium group and at least one C8 C22 alkyl group. Other suitable emulsifiers are compounds of the general formula 8 56 R S0 3 X S0 3 y in which R 5 and R are hydrogen or C4 to C14 alkyl but are not simultaneously hydrogen, and X and Y can be alkali metal ions and/or ammonium ions. Preferably R 5 ,

R

6 are linear or branched alkyl radicals having 6 to 18 C atoms or hydrogen, and more 5 particularly having 6, 12, and 16 C atoms, with R 5 and R 6 not both simultaneously being hydrogen. X and Y are preferably sodium, potassium or ammonium ions, with sodium being particularly preferred. Particularly advantageous compounds Il are those in which X and Y are sodium, R 5 is a branched alkyl radical having 12 C atoms, and R 6 is hydrogen or R 5 . Oftentimes use is made of technical mixtures which comprise a 10 fraction of 50% to 90% by weight of the monoalkylated product, an example being Dowfax*2A1 (trade mark of the Dow Chemical Company). Suitable emulsifiers are also found in Houben-Weyl, Methoden der organischen Chemie, volume 14/1, Makromolekulare Stoffe, Georg Thieme Verlag, Stuttgart, 1961, pages 192 to 208. Examples of emulsifier trade names include Dowfax@2 Al, Emulan* NP 50, Dextrol* 15 OC 50, Emulgator 825, Emulgator 825 S, Emulan*OG, Texapon* NSO, Nekanil* 904 S, Lumiten* I-RA, Lumiten* E 3065, DisponilO FES 77, Lutensol* AT 18, Steinapol* VSL, and Emulphor* NPS 25. Also suitable are copolymerizable emulsifiers which comprise a free-radically polymerizable, ethylenically unsaturated double bond, examples being reactive anionic emulsifiers such as Adeka@ Resoap SR-10. 20 The emulsion polymerization takes place in general at 30 to 130, preferably 50 to 90*C. The polymerization medium may be composed either only of water or else of mixtures of water and water-miscible liquids such as methanol. It is preferred to use just water. The emulsion polymerization can be carried out either as a batch operation or in the 25 form of a feed process, including staged or gradient procedures. Preference is given to the feed process, in which a portion of the polymerization batch is made the initial charge, heated to the polymerization temperature, and partially polymerized, and then the remainder of the polymerization batch, usually by way of two or more spatially separate feeds, of which one or more comprise the monomers in pure form or in 30 emulsified form, is supplied continuously or else in stages. The emulsion polymerization is carried out in the presence of at least one protective colloid. This means that the protective colloids are included in the initial charge or supplied together with monomers to the polymerization vessel. They are preferably 35 included in the initial emulsion polymerization charge, while any additionally employed emulsifiers may also be supplied together with the monomers in the course of the polymerization.

9 For the emulsion polymerization it is possible to use the customary and known auxiliaries, such as water-soluble initiators and regulators, for example. Examples of water-soluble initiators for the emulsion polymerization are ammonium salts and alkali metal salts of peroxodisulfuric acid, e.g., sodium peroxodisulfate, hydrogen peroxide or 5 organic peroxides, e.g., tert-butyl hydroperoxide. Also suitable are what are called reduction-oxidation (redox) initiator systems. The redox initiator systems are composed of at least one, usually inorganic, reducing agent and one organic or inorganic oxidizing agent. The oxidizing component comprises, for example, the initiators already specified above for the emulsion polymerization. The reducing components are, for example, 10 alkali metal salts of sulfurous acid, such as sodium sulfite, sodium hydrogen sulfite, alkali metal salts of disulfurous acid such as sodium disulfite, bisulfite addition compounds with aliphatic aldehydes and ketones, such as acetone bisulfite, or reducing agents such as hydroxymethanesulfinic acid and salts thereof, or ascorbic acid. The redox initiator systems may be used in the company of soluble metal 15 compounds whose metallic component is able to exist in a plurality of valence states. Typical redox initiator systems are, for example, ascorbic acid/iron(II) sulfate/sodium peroxodisulfate, tert-butyl hydroperoxide/sodium disulfite, tert-butyl hydroperoxide/Na hydroxymethanesulfinate, or tert-butyl hydroperoxide/ascorbic acid. The individual components, the reducing component for example, may also be mixtures, an example 20 being a mixture of the sodium salt of hydroxymethanesulfinic acid with sodium disulfite. The stated compounds are used usually in the form of aqueous solutions, with the lower concentration being determined by the amount of water that is acceptable in the dispersion, and the upper concentration by the solubility of the respective compound in water. Generally speaking, the concentration is 0.1% to 30%, preferably 0.5% to 20%, 25 more preferably 1.0% to 10%, by weight, based on the solution. The amount of the initiators is generally 0.1% to 10% by weight, preferably 0.5% to 5% by weight, based on the monomers to be polymerized. It is also possible for two or more different initiators to be used in the emulsion polymerization. For the removal of the residual monomers, it is usual to add initiator after the end of the actual emulsion polymerization 30 as well. In the polymerization it is possible to use regulators, in amounts, for example, of 0 to 0.8 part by weight, based on 100 parts by weight of the monomers to be polymerized, these regulators reducing the molar mass. Suitable examples include compounds 35 having a thiol group such as tert-butyl mercaptan, thioglycolic acid ethylacrylic esters, mercaptoethanol, mercaptopropyltrimethoxysilane or tert-dodecyl mercaptan. Additionally it is possible to use regulators without a thiol group, such as terpinolene, for example. In one preferred embodiment the emulsion polymer is prepared using 0.05% to 0.5% by weight, based on the monomer amount, of at least one molecular 40 weight regulator. In one embodiment of the invention the composition is one in which the emulsion 10 polymer prepared by emulsion polymerization is a straight acrylate or a styrene acrylate, i.e., is composed exclusively of alkyl (meth)acrylate monomers or of a combination of alkyl (meth)acrylate monomers and styrene, the alkyl group preferably having 1 to 8 C atoms and preferably at least one monomer being ethyl acrylate or n 5 butyl acrylate. One embodiment of the invention provides a recloseable pack wherein the emulsion polymer used for cold sealing and prepared by emulsion polymerization in the presence of a protective colloid has a glass transition temperature of -30 to 0*C and is 10 formed 100% of monomers selected from acrylic esters, methacrylic esters, styrene, and a mixture thereof, and the protective colloid (i) is used in an amount of 7 to 30% by weight, based on the amount of the emulsion polymer, (ii) is composed to an extent of at least 40% by weight of principal monomers 15 selected from the group consisting of C1 to C20 alkyl (meth)acrylates, styrene, alpha-methylstyrene, and a mixture thereof, (iii) is composed to an extent of at least 15% by weight of ethylenically unsaturated acid monomers preferably selected from acrylic acid, methacrylic acid, and a mixture thereof, and 20 (iv) has a number-average molecular weight of 1000 to 10 000. The invention also provides a composition in the form of an aqueous polymer dispersion being suitable for producing cold-sealable, recloseable packaging materials, and the polymer dispersion being preparable by emulsion polymerization of free 25 radically polymerizable monomers in the presence of at least one protective colloid, where the emulsion polymer prepared by emulsion polymerization has a glass transition temperature of -30 to 00C and is formed 100% of monomers selected from acrylic esters, methacrylic esters, styrene, and a mixture thereof, and the protective colloid 30 (i) is used in an amount of 7 to 30% by weight, based on the amount of the emulsion polymer, (ii) is composed to an extent of at least 40% by weight of principal monomers selected from the group consisting of C1 to C20 alkyl (meth)acrylates, styrene, alpha-methylstyrene, and a mixture thereof, 35 (iii) is composed to an extent of at least 15% by weight of ethylenically unsaturated acid monomers preferably selected from acrylic acid, methacrylic acid, and a mixture thereof, and (iv) has a number-average molecular weight of 1000 to 10 000. 40 This composition is preferably used to produce the pack of the invention. The polymer dispersion of this composition, following application to a substrate and following drying, forms a coating which at room temperature is autoadhesive and is blocking-resistant 11 with respect to polyamide surfaces. The invention also provides for the use of the aqueous polymer dispersions described above for producing a cold-sealable pack which is recloseable after initial opening. 5 Following application to a substrate and following drying, the polymer dispersion forms a coating which at room temperature is blocking-resistant and is autoadhesive. The composition of the invention is suitable for cold-sealing two arbitrary substrates, in which case 10 - the two substrates, at the points which are to be adhered, having been or being each coated with the composition of the invention, and - the two substrates, if desired with exertion of pressure, being contacted, the temperature in the coated composition being less than 40*C (cold sealing; see above). 15 Substrates contemplated for bonding include any desired substrates, examples being substrates made of wood, metal, paper or plastic, which may be bonded to one another in any desired combination, at least one substrate preferably being a polymer film. For this purpose the substrates are coated with the composition of the invention. Coating 20 may take place in a conventional manner, as for example by printing, more particularly by flexographic printing or by gravure printing (intaglio printing). Customary coat thicknessses (after drying) are, for example, 1 to 30 g/m 2 , preferably 1 to 10 g/m 2 or 1 to 5 g/m 2 . The composition of the invention is suitable especially for producing packaging. Packaging contemplated is that composed of any desired materials, such 25 as of paper or, preferably, of plastic, for example. Examples cited may include packaging made from polymer films, including, if desired, metallized polymer films, e.g., of polyethylene, polypropylene, PVC, polyester and/or polyacetate. Especially suitable for producing packaging is a double-sidedly coated carrier, the 30 carrier having on one side (referred to below as face) an outer layer of the composition of the invention, and having on the other side (referred to below as reverse) an outer release coating. The carrier may be composed, for example, of one of the abovementioned polymer films, or metallized polymer films, mention being made in particular of films of oriented polypropylene, polyethylene, preferably high-density 35 polyethylene, or polyethylene terephthalate. The polymer films may also have been corona-pretreated. The composition of the invention may be coated directly onto the face of the carrier, although between the carrier and the composition of the invention there may also be other layers, examples being primer layers, barrier layers or colored or monochrome printing-ink layers, although printing ink layers are preferably located 40 on the reverse of the carrier. It is essential that the layer of the composition of the invention be located on the outside.

12 The release coating may be of any desired material, and may be a polymer film, e.g., a film of oriented polypropylene, which is laminated on or coextruded, or a liquid varnish, such as a polyamide varnish, for example, which is applied and filmed; it is essential that the layer of adhesive applied to the face of the carrier (in the present case, the 5 composition of the invention) does not adhere to the release coating (blocking resistance). The carrier is generally rolled up and later processed from the roll. In the course of rolling, the face and the reverse of the carrier come into direct contact. Adhesion of the face to the reverse would make the carrier unusable. Between the release coating and the carrier there may be further layers; those contemplated 10 include, in turn, layers of a primer which improves the adhesion, and printing ink layers. Another function of the outer release coating is to protect the lower layers, more particularly the printing ink layer, from external exposures. Preferred carriers have the following construction, the sequence of the layers 15 corresponds to the spatial arrangement: adhesive layer (composition of the invention) carrier optional primer layer optional printing ink layer 20 release coating. The double-sidedly coated carrier is used more particularly for producing packaging, for which purpose it is preferably bonded to itself by cold sealing, with the faces coated with the outer composition of the invention being brought into contact in each case. It is 25 essential here that both carriers to be bonded are coated with the composition of the invention at the points that are to be bonded and that form the subsequent sealed seam. The packaging is sealed together by cold sealing of the adhesive layer as soon as the packaged contents have been introduced. The packaging is suitable especially for comestibles. 30 In the cold-sealed, recloseable pack of the invention, the cold sealing is formed preferably between a first and a second closure section, the bonding force of the cold seal to the first and second sections being greater than the bonding force within the cold seal, so that the cold seal is parted and bonds partly to the first and partly to the 35 second closure section when the closure is opened; in other words, when the pack is opened, there is cohesive fracture of the sealing layer. When the pack is being produced, the composition used for the cold seal is applied preferably in an amount of 2 to 5 g/m 2 (based on solids) to each closure section. 40 The closure forces of the pack of the invention are preferably such that the initial opening force is at least 2 N/15 mm, preferably 2.5 to 5 N/15 mm, measured in 13 accordance with the method described in the examples. The opening force for one or more reclosing operations is preferably at least 0.5 N/1 5 mm, preferably 0.5 to 2 N/15 mm or 1 to 1.5 N/15 mm, measured in accordance with the method described in the examples. 5 Also provided by the invention is a coated polymer film, where a polymer carrier film is coated at least partly, i.e., at least at the areas forming the subsequent sealed seam, with a composition of the invention. The polymer film of the invention preferably has a first side and a second side, the first side as outer layer being coated at least partly 10 with a composition of the invention, and the second side having as outer layer a release coating. In one embodiment the polymer carrier film of the coated polymer film of the invention is composed of polyethylene or oriented polypropylene, and the release coating is formed on the basis of polyamide. 15 The invention also provides for the use of the coated polymer film of the invention for producing packaging, more particularly film packaging for comestibles. The invention also provides a method for producing a recloseable, cold-sealed pack, in which a composition of the invention as described in more detail above is applied in the 20 form of an aqueous polymer dispersion to a packaging substrate and is dried and cold sealed. Examples 25 Unless the context dictates otherwise, the figures in percent always denote percent by weight. A content datum relates to the content in aqueous solution or dispersion. The ingredients used were as follows: Oppalyte@ 33MW247: film recommended for cold-seal applications, made of surface 30 treated, biaxially oriented polypropylene, from Exxon Mobil Corp. Treofan@ SHD40: film recommended for cold-seal applications, made of oriented polypropylene, from Treofan GmbH & Co. KG Gecko@ Coldseal Release varnish 70 GL 282547: polyamide release varnish, solvent based, from Huber Group 35 Cold-seal testing Coating with polyamide release varnish A 0.07mm wire applicator is used to apply Gecko@ Coldseal Release varnish 70 GL 40 282547 to the pretreated side of the OPP film SHD40, and the applied varnish is dried with hot air for 10 seconds. Release varnish application rate: about 1.0 g/m 2

.

14 Coating of the OPP film With the bar applicator, the adhesive is applied to the pretreated side of the OPP film Oppalyte @ 33MW247 and dried at 70 0 C for 1 minute. The coated film is lined with an OPP film coated with release varnish. 5 Sealed seam strength (SSS) Strips 15 mm wide are cut from the coated film and sealed to one another (adhesive to adhesive) on the sealing device for 0.5 second with 200 N (1.4 bar). 30 seconds after sealing has taken place, the peel strengths in N/15 mm are ascertained at a peel speed 10 of 50 mm/min. Blocking test The coated film is placed against the release-varnish-coated side of an SHD40 OPP film, and a circular section having a diameter of 10 cm is loaded with 10 tonnes for 15 1 day. Thereafter the peel strengths of strips 25 mm wide are determined in N/25 mm, with a peel speed of 800 mm/min. Reclose strength The test specimens are produced as for the testing of the sealed seam strength, and 20 are likewise sealed to one another. The seal is then opened and closed again five times by hand. For closing, a manual roller weighing 2 kg is rolled once back and once forth over the seal in each case. The sealed seam strength determined then is the reclose strength after five fold closing. 25 All tests take place at room temperature (20*C). Example BI Poly(ethyl acrylate), prepared by emulsion polymerization in the presence of 0.2 part by weight (based on 100 parts by weight of monomer) of t-dodecyl mercaptan and also in 30 the presence of a protective colloid having a number-average molecular weight of 4000, prepared from 44 parts by weight of acrylic acid and 56 parts by weight of n-butyl acrylate. Glass transition temperature: -25*C. 35 Example B2 Poly(ethyl acrylate), prepared by emulsion polymerization in the presence of 0.2 part by weight (based on 100 parts by weight of monomer) of t-dodecyl mercaptan and also in the presence of a protective colloid having a number-average molecular weight of 9000, prepared from 32 parts by weight of acrylic acid, 24 parts by weight of styrene, 40 33 parts by weight of alpha-methylstyrene, 5 parts by weight of ethylhexyl acrylate, and 5 parts by weight of isooctyl acrylate. Glass transition temperature: -25"C.

15 Example B3 Poly(ethyl acrylate), prepared by emulsion polymerization in the presence of 0.2 part by weight (based on 100 parts by weight of monomer) of t-dodecyl mercaptan and also in 5 the presence of a protective colloid having a number-average molecular weight of 9200, prepared from 33 parts by weight of acrylic acid, 32 parts by weight of styrene, 30 parts by weight of alpha-methylstyrene, and 5 parts by weight of isooctyl acrylate. Glass transition temperature: -25 0 C. 10 Example B4 Copolymer of 70 parts by weight of n-butyl acrylate and 30 parts by weight of styrene, prepared by emulsion polymerization in the presence of 0.2 part by weight (based on 100 parts by weight of monomer) of t-dodecyl mercaptan and also in the presence of a protective colloid having a number-average molecular weight of 4000, prepared from 15 44 parts by weight of acrylic acid and 56 parts by weight of n-butyl acrylate. Glass transition temperature: -15*C. Example B5 Like Example B1, without t-dodecyl mercaptan. 20 Comparative example C1 Commercial natural rubber latex NK Latex from Eukalin, solids content 55% 25 Comparative example C2 Copolymer of 70 parts by weight of ethyl acrylate and 30 parts by weight of styrene, prepared by emulsion polymerization in the presence of 0.2 part by weight (based on 100 parts by weight of monomer) of t-dodecyl mercaptan and also in the presence of a protective colloid having a number-average molecular weight of 4000, prepared from 30 44 parts by weight of acrylic acid and 56 parts by weight of n-butyl acrylate. Glass transition temperature: +5 0 C. Comparative example C3 Copolymer of 44 parts by weight of ethyl acrylate and 56 parts by weight of n-butyl 35 acrylate, prepared by emulsion polymerization in the presence of 0.2 part by weight (based on 100 parts by weight of monomer) of t-dodecyl mercaptan and also in the presence of a protective colloid having a number-average molecular weight of 4000, prepared from 44 parts by weight of acrylic acid and 56 parts by weight of n-butyl acrylate. 40 Glass transition temperature: -36*C. Comparative example C4 16 Like Example B1, prepared by emulsion polymerization in the presence of emulsifiers, without protective colloid. The results of the cold-sealing tests are set out in Table 1. 5 Table 1: Results of the cold-sealing tests Sealed seam Blocking resistance Reclose strength after 5-fold strength with respect to release reclosing [N/15 mm] [N/15 mm] coating [N/25 mm] B1 4.0 0.05 1.0 B2 2.6 0.06 0.9 B3 3.0 0.05 1.0 B4 2.3 0.1 0.8 B5 3.0 0.06 1.0 C1 2.0 0.0 0.0 C2 0.7 0.0 0.0 C3 0.7 0.43 0.5 C4 0.8 0.07 0.4 The inventive compositions B1 to B5 are notable relative to the comparative compositions C1 to C4 for an unexpected combination of advantageous properties, 10 including a high sealed seam strength of more than 2 N/15 mm, good blocking resistance of not more than 0.1 N/25 mm, and a high reclose strength of more than 0.5 N/15 mm. Comprises/comprising and grammatical variations thereof when used in this 15 specification are to be taken to specify the presence of stated features, integers, steps or components or groups thereof, but do not preclude the presence or addition of one or more other features, integers, steps, components or groups thereof.

Claims

1. A recloseable pack having a cold-sealed layer of adhesive which is recloseable after the pack has been opened, the layer of adhesive comprising an emulsion 5 polymer composed to an extent of at least 60% by weight of principal monomers selected from the group consisting of C1 to C20 alkyl (meth)acrylates, vinyl esters of carboxylic acids comprising up to 20 C atoms, vinylaromatics having up to 20 C atoms, ethylenically unsaturated nitriles, vinyl halides, vinyl ethers of alcohols comprising 1 to 10 C atoms, aliphatic hydrocarbons having 2 to 8 C atoms and one 10 or two double bonds, and mixtures of these monomers, the emulsion polymer being preparable by emulsion polymerization of free-radically polymerizable monomers in the presence of at least one protective colloid and having a glass transition temperature in the range from -30 to O'C. 15

2. The recloseable pack according to the preceding claim, wherein the emulsion polymer prepared by emulsion polymerization is free from acid groups.

3. The recloseable pack according to either of the preceding claims, wherein the emulsion polymer prepared by emulsion polymerization is composed to an extent 20 of 60% to 100% by weight of at least one C 1 to C 20 alkyl acrylate, at least one C 1 to C 20 alkyl methacrylate, a mixture thereof, or a mixture thereof with styrene.

4. The recloseable pack according to any one of the preceding claims, wherein the cold seal is formed between a first and a second closure section, the bonding force 25 of the cold seal to the first and second sections being greater than the bonding force within the cold seal, so that the cold seal is parted and bonds partly to the first and partly to the second closure section when the closure is opened.

5. The recloseable pack according to any one of the preceding claims, wherein the 30 pack features an initial opening force of at least 2 N/1 5 mm and also opening forces for one or more reclosing operations of at least 0.5 N/15 mm.

6. The recloseable pack according to any one of the preceding claims, wherein the cold seal is applied in an amount of 2 to 5 g/m 2 to each closure section. 35

7. The recloseable pack according to any one of the preceding claims, wherein the protective colloid (i) is used in an amount of 7% to 30% by weight, based on 100 parts by weight of the monomers to be polymerized, 40 (ii) is composed to an extent of at least 40% by weight of principal monomers selected from the group consisting of C1 to C20 alkyl (meth)acrylates, vinyl esters of carboxylic acids comprising up to 20 C atoms, vinylaromatics having up to 20 C atoms, ethylenically unsaturated nitriles, vinyl halides, vinyl ethers 18 of alcohols comprising 1 to 10 C atoms, aliphatic hydrocarbons having 2 to 8 C atoms and one or two double bonds, and mixtures of these monomers, (iii) is composed to an extent of at least 15% by weight of ethylenically unsaturated acid monomers preferably selected from acrylic acid, methacrylic acid, and a 5 mixture thereof, and (iv) has a number-average molecular weight of 1000 to 10 000.

8. The recloseable pack according to any one of the preceding claims, wherein the emulsion polymer is prepared using 0.05% to 0.5% by weight, based on the 10 monomer amount, of at least one molecular weight regulator.

9. The recloseable pack according to any one of the preceding claims, wherein the autoadhesion of the layer of adhesive after cold sealing at 200C and 1.4 bar is at least 2 N/15 mm and the adhesion of the unsealed layer of adhesive with respect 15 to a polyamide surface after loading of a circular surface with a diameter of 10 cm with 10 tonnes for one day at 20*C is not more than 0.1 N/25 mm.

10. The recloseable pack according to any one of the preceding claims, wherein the emulsion polymer prepared by emulsion polymerization has a glass transition 20 temperature of -30 to 0*C and is formed 100% of monomers selected from acrylic esters, methacrylic esters, styrene, and a mixture thereof, and the protective colloid (i) is used in an amount of 7% to 30% by weight, based on the amount of the emulsion polymer, (ii) is composed to an extent of at least 40% by weight of principal monomers 25 selected from the group consisting of C1 to C20 alkyl (meth)acrylates, styrene, alpha-methylstyrene, and a mixture thereof, (iii) is composed to an extent of at least 15% by weight of ethylenically unsaturated acid monomers preferably selected from acrylic acid, methacrylic acid, and a mixture thereof, and 30 (iv) has a number-average molecular weight of 1000 to 10 000.

11. The recloseable pack according to any one of the preceding claims, wherein the emulsion polymerization takes place in the presence of the protective colloid without addition of a nonpolymeric emulsifier. 35

12. A composition in the form of an aqueous polymer dispersion, the aqueous polymer dispersion being suitable for producing cold-sealable, recloseable packaging materials, and the polymer dispersion being preparable by emulsion polymerization of free-radically polymerizable monomers in the presence of at least one protective 40 colloid, where the emulsion polymer prepared by emulsion polymerization has a glass transition temperature of -30 to 0*C and is formed 100% of monomers selected from acrylic esters, methacrylic esters, styrene, and a mixture thereof, and 19 the protective colloid (i) is used in an amount of 7% to 30% by weight, based on the amount of the emulsion polymer, (ii) is composed to an extent of at least 40% by weight of principal monomers 5 selected from the group consisting of C1 to C20 alkyl (meth)acrylates, styrene, aIpha-methylstyrene, and a mixture thereof, (iii) is composed to an extent of at least 15% by weight of ethylenically unsaturated acid monomers preferably selected from acrylic acid, methacrylic acid, and a mixture thereof, and 10 (iv) has a number-average molecular weight of 1000 to 10 000; wherein the polymer dispersion, following application to a substrate and following drying, forms a coating which at room temperature is autoadhesive and is blocking resistant with respect to polyamide surfaces. 15

13. A coated polymer film wherein a polymer carrier film is at least partly coated with a composition according to claim 12.

14. The coated polymer film according to the preceding claim, wherein the polymer film 20 has a first side and a second side, the first side being coated, as an outer layer, at least partly with a composition according to claim 12, and the second side having, as an outer layer, a release coating.

15. The coated polymer film according to either of the two preceding claims, wherein 25 the polymer carrier film is composed of polyethylene or oriented polypropylene and the release coating is formed on the basis of polyamide.

16. The use of an aqueous polymer dispersion for producing a cold-sealable pack which is recloseable after initial opening, the polymer dispersion comprising a 30 water-dispersed emulsion polymer which is composed to an extent of at least 60% by weight of principal monomers selected from the group consisting of C1 to C20 alkyl (meth)acrylates, vinyl esters of carboxylic acids comprising up to 20 C atoms, vinylaromatics having up to 20 C atoms, ethylenically unsaturated nitriles, vinyl halides, vinyl ethers of alcohols comprising 1 to 10 C atoms, aliphatic 35 hydrocarbons having 2 to 8 C atoms and one or two double bonds, and mixtures of these monomers, the emulsion polymer being preparable by emulsion polymerization of free-radically polymerizable monomers in the presence of at least one protective colloid and having a glass transition temperature in the range from -30 to 0*C. 40

17. The use according to the preceding claim, wherein the polymer dispersion, following application to a substrate and following drying, forms a coating which at 20 room temperature is blocking-resistant and is autoadhesive.

18. The use according to either of the two preceding claims, wherein the substrate is a polymer film. 5

19. A method for producing a recloseable, cold-sealed pack, where a composition in the form of an aqueous polymer dispersion is applied to a packaging substrate, dried, and cold-sealed, the composition comprising an emulsion polymer which is composed to an extent of at least 60% by weight of principal monomers selected 10 from the group consisting of C1 to C20 alkyl (meth)acrylates, vinyl esters of carboxylic acids comprising up to 20 C atoms, vinylaromatics having up to 20 C atoms, ethylenically unsaturated nitriles, vinyl halides, vinyl ethers of alcohols comprising 1 to 10 C atoms, aliphatic hydrocarbons having 2 to 8 C atoms and one or two double bonds, and mixtures of these monomers, the emulsion polymer 15 being preparable by emulsion polymerization of free-radically polymerizable monomers in the presence of at least one protective colloid and having a glass transition temperature in the range from -30 to 0*C.

20. A recloseable pack as claimed in any one of claims 1 to 11 and as described 20 herein with reference to the examples.