WO1998006571A1 - Feuille multicouche composite d'une bonne aptitude au compostage, son procede de fabrication et son utilisation - Google Patents

Feuille multicouche composite d'une bonne aptitude au compostage, son procede de fabrication et son utilisation Download PDF

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Publication number
WO1998006571A1
WO1998006571A1 PCT/EP1997/004389 EP9704389W WO9806571A1 WO 1998006571 A1 WO1998006571 A1 WO 1998006571A1 EP 9704389 W EP9704389 W EP 9704389W WO 9806571 A1 WO9806571 A1 WO 9806571A1
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Prior art keywords
films
polyester
barrier layer
multilayer film
biodegradable
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PCT/EP1997/004389
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German (de)
English (en)
Inventor
Frank-Martin Neumann
Original Assignee
Sengewald Verpackungen Gmbh
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Application filed by Sengewald Verpackungen Gmbh filed Critical Sengewald Verpackungen Gmbh
Priority to EP97942856A priority Critical patent/EP0918632A1/fr
Priority to AU44544/97A priority patent/AU4454497A/en
Publication of WO1998006571A1 publication Critical patent/WO1998006571A1/fr

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    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B27/00—Layered products comprising a layer of synthetic resin
    • B32B27/06—Layered products comprising a layer of synthetic resin as the main or only constituent of a layer, which is next to another layer of the same or of a different material
    • B32B27/08—Layered products comprising a layer of synthetic resin as the main or only constituent of a layer, which is next to another layer of the same or of a different material of synthetic resin
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
    • A61L15/00—Chemical aspects of, or use of materials for, bandages, dressings or absorbent pads
    • A61L15/16—Bandages, dressings or absorbent pads for physiological fluids such as urine or blood, e.g. sanitary towels, tampons
    • A61L15/22—Bandages, dressings or absorbent pads for physiological fluids such as urine or blood, e.g. sanitary towels, tampons containing macromolecular materials
    • A61L15/24—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds; Derivatives thereof
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
    • A61L15/00—Chemical aspects of, or use of materials for, bandages, dressings or absorbent pads
    • A61L15/16—Bandages, dressings or absorbent pads for physiological fluids such as urine or blood, e.g. sanitary towels, tampons
    • A61L15/22—Bandages, dressings or absorbent pads for physiological fluids such as urine or blood, e.g. sanitary towels, tampons containing macromolecular materials
    • A61L15/26—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds; Derivatives thereof
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
    • A61L15/00—Chemical aspects of, or use of materials for, bandages, dressings or absorbent pads
    • A61L15/16—Bandages, dressings or absorbent pads for physiological fluids such as urine or blood, e.g. sanitary towels, tampons
    • A61L15/42—Use of materials characterised by their function or physical properties
    • A61L15/62—Compostable, hydrosoluble or hydrodegradable materials
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B27/00—Layered products comprising a layer of synthetic resin
    • B32B27/30—Layered products comprising a layer of synthetic resin comprising vinyl (co)polymers; comprising acrylic (co)polymers
    • B32B27/306—Layered products comprising a layer of synthetic resin comprising vinyl (co)polymers; comprising acrylic (co)polymers comprising vinyl acetate or vinyl alcohol (co)polymers
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B27/00—Layered products comprising a layer of synthetic resin
    • B32B27/36—Layered products comprising a layer of synthetic resin comprising polyesters
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B7/00—Layered products characterised by the relation between layers; Layered products characterised by the relative orientation of features between layers, or by the relative values of a measurable parameter between layers, i.e. products comprising layers having different physical, chemical or physicochemical properties; Layered products characterised by the interconnection of layers
    • B32B7/04—Interconnection of layers
    • B32B7/12—Interconnection of layers using interposed adhesives or interposed materials with bonding properties
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B65—CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
    • B65D—CONTAINERS FOR STORAGE OR TRANSPORT OF ARTICLES OR MATERIALS, e.g. BAGS, BARRELS, BOTTLES, BOXES, CANS, CARTONS, CRATES, DRUMS, JARS, TANKS, HOPPERS, FORWARDING CONTAINERS; ACCESSORIES, CLOSURES, OR FITTINGS THEREFOR; PACKAGING ELEMENTS; PACKAGES
    • B65D65/00—Wrappers or flexible covers; Packaging materials of special type or form
    • B65D65/38—Packaging materials of special type or form
    • B65D65/46—Applications of disintegrable, dissolvable or edible materials
    • B65D65/466—Bio- or photodegradable packaging materials
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2250/00—Layers arrangement
    • B32B2250/24—All layers being polymeric
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2307/00—Properties of the layers or laminate
    • B32B2307/70—Other properties
    • B32B2307/716—Degradable
    • B32B2307/7163—Biodegradable
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2553/00—Packaging equipment or accessories not otherwise provided for
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02W—CLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO WASTEWATER TREATMENT OR WASTE MANAGEMENT
    • Y02W90/00—Enabling technologies or technologies with a potential or indirect contribution to greenhouse gas [GHG] emissions mitigation
    • Y02W90/10—Bio-packaging, e.g. packing containers made from renewable resources or bio-plastics

Definitions

  • the invention relates to a well compostable composite multilayer film comprising at least one barrier layer made of polyvinyl alcohol, to which one or more films are laminated on both sides by means of an adhesive or applied by means of coextrusion or by hot coating, a method for producing such multilayer films and their use.
  • Thermoplastic processable and biodegradable materials for biodegradable (compostable) films are already known, for example from EP-0-641 817 A2.
  • polyesteramides are disclosed, for example, from adipic acid, butanediol and aminocarboxylic acid with an ester content of 45% by weight, which in the biological degradation test show a large microbial growth of, for example, 102 mg in 14 days.
  • a sample is also referred to as well compostable, which, under certain conditions, enables a biomass growth of at least 30 mg / l on the polymers within a maximum of two weeks.
  • the prior art also includes mixed polyurethane prepolymers which can be used as adhesives for laminating film materials, as they are made of EP 0 150 444 B1 are accessible.
  • These polyurethane prepolymers have terminal isocyanate groups from diisocyanates of different reactivity and polyfunctional alcohols, and are suitable in bulk or in aqueous solution for bonding plastics, in particular for laminating plastic films. It is known that the products obtainable with such polyurethane prepolymers (manufactured film composites) show a high level of processing reliability when heat-sealing. This may be attributed to a reduced proportion of low molecular weight products capable of migration in the prepolymers.
  • the invention has now set itself the task of providing a polyethylene or polyolefin film replacement in general, which contains a corresponding barrier layer, so that all the requirements for barrier films are met and which still fulfills all processing requirements for a film composite and at the same time is outstandingly biological is degradable (compostable). Furthermore, a method for producing such biodegradable multilayer films is to be specified. Finally, the present invention also relates to the use of the well rot and compostable films.
  • a multilayer film which has at least one polyvinyl alcohol film as the barrier layer and on both sides of the barrier layer has at least one film consisting of biodegradable aliphatic polyester amides and / or biodegradable polyesters which are connected to the polyvinyl alcohol layer by hot coating or laminated thereon by means of an adhesive to provide a multilayer film which has excellent biodegradability (compostability).
  • compostability of the multi-layer film is better than the compostability of the materials involved in the construction of the multi-layer film, seen in isolation.
  • the most poorly compostable component for example the layer made of polyester amide and / or polyester
  • compostability is understood to mean a property of the individual materials used and of the entire composite, that is to say the composite multilayer film, the compostability being in a specific connection to the biodegradability.
  • compostability means biodegradability in the soil under composting conditions.
  • Biodegradable polymers and plastics are materials that are quantitatively converted into either CO 2 and H 2 O or CH 4 and H 2 O by microorganisms under aerobic or anaerobic conditions.
  • good compostability means that a material in the biodegradation test according to ASTM G22 produces> 30 mg / 1 biomass. In a preferred embodiment of the invention, this is met or exceeded both by the individual layers and by the composite as a whole. The measuring method is explained in more detail in the example section.
  • the barrier PVOH layer is laminated with the aliphatic polyester amide and / or polyester layer (s) by means of a polyurethane adhesive
  • the polyurethane adhesive used also has excellent biodegradability (compostability). This was previously unknown and cannot be expected based on the data available.
  • the invention thus provides a film which can be used universally as a polyolefin film substitute for a variety of purposes.
  • the basic structure of the film according to the invention with a core of polyvinyl alcohol as a barrier layer and film layers of biodegradable goods surrounding this core from both sides, in particular of aliphatic polyester amides and / or polyesters, can be used universally and can be modified in many ways. Among other things, it is possible to apply a thin aluminum layer (a few nanometers) to the biodegradable goods by vapor deposition or sputtering, this thin aluminum layer acting as an aroma sealing layer. Even the most sensitive substances (vanillin) do not lose their aroma when wrapped in the appropriate foil.
  • a thin aluminum layer in the range of a few nanometers is readily environmentally compatible, since it can be assumed that, for example, aluminum is converted to oxides or hydroxides, which do not stand in the way of compostability.
  • a combination with paper goods, for example in the form of superabsorbers, is also conceivable.
  • the film according to the invention can be used as a polyethylene or polypropylene substitute in hygiene goods, for example diapers, sanitary napkins, etc.
  • the films according to the invention have excellent processing properties, are extrudable, optionally coextrudable, and can be stretched not only individually but also in combination, for example a multilayer film according to the invention can be stretched biaxially.
  • the core of the material according to the invention is in any case a film layer made of polyvinyl alcohol.
  • Such materials are familiar to the person skilled in the art and can be produced, for example, by saponification of polyvinyl acetate. It is known that such films made of polyvinyl alcohol are largely impenetrable for gases such as oxygen, nitrogen, carbon dioxide etc., but that they do allow water vapor to pass through.
  • gases such as oxygen, nitrogen, carbon dioxide etc.
  • Various characteristics can be used to characterize polyvinyl alcohol, which is generally free of residual monomers as a commercial product Partial and full saponification.
  • the fully hydrolyzed (fully hydrolyzed) vinyl acetate polymer corresponds to the basic building block of the PVOH.
  • the partial saponification leads to a polymer of -CH 2 -CH (OH) - and -CH 2 -CH (OCOH 3 ) - building blocks
  • the molecular weight, expressed in Mw which is 1.7 x 10 5 to 2.5 x 10 5 for highly viscous, fully saponified types and only 1 x 10 4 - 6 x 10 4 for low-viscosity types.
  • polyvinyl alcohol generally has excellent biodegradability, which can be demonstrated for aqueous PVOH solutions in a test with adapted activated sludge, the PVOH elimination from water generally being determined by determining the chemical oxygen demand (COD).
  • PVOH films are also biodegradable, measured in the Zahn-Wellens test. Both findings are therefore a clear indication of excellent compostability, although this depends to a certain extent on the degree of saponification of the polyvinyl acetate. For example, a certain residual concentration of acetate groups has proven to be beneficial for biodegradability, in particular compostability.
  • the thickness of the core layer made of polyvinyl alcohol is not particularly critical in the context of the multilayer film structure according to the invention. It can be varied beyond the usual values and is preferably in the range from about 3-20 .mu.m.
  • Thicknesses in the range between 5 and 12 ⁇ m are particularly preferred.
  • particularly useful barrier layers result if the PVOH fulfills one or more of the following criteria:
  • Mw between 14,000 and 210,000, preferably between 14,000 and 175,000, particularly preferably between 18,000 and 175,000;
  • Viscosity between 3 and 60 mPa.s, preferably between 3 and 40 mPa.s, particularly preferably between 5 and 40 mPa.s;
  • PVOH grades include the Mowiol® ® from Hoechst.:
  • Polyesteramide materials which are suitable for films which are suitable in combination with polyvinyl alcohol films in the context of the invention generally have relatively high molecular weights with ester contents between 30 and 70% by weight, are easy and reproducible to produce and have good mechanical properties also for the production of transparent films and good biodegradability or compostability. Such materials are known for example from EP 0 641 817 A2.
  • the aliphatic polyester amides have aliphatic ester and aliphatic amide structures and have melting points of at least 75 ° C. The weight fraction of the ester structures is between 30 and 70%, the proportion of the amide structures between 70 and 30%.
  • the copolymers suitable for the production of the films have an average molecular weight (MW determined by gel chromatography in m-cresol against standard polystyrene) of 10,000 to 300,000, preferably 20 to 150,000.
  • Such polyester amides are preferably synthesized by mixing the amides or ester-forming starting components and polymerization at elevated temperature under autogenous pressure and then distilling off the water of reaction and excess monomers in vacuo and at elevated temperature.
  • the arrangement of the ester or amide segments is carried out purely statistically by the synthesis conditions, ie these compounds are not to be referred to as thermoplastic elastomers but as thermoplastics.
  • the structure of thermoplastic elastomers is described in the specialist literature with "the simultaneous presence of soft and elastic segments with high ductility and low glass transition temperature (to Tg value) as well as hard and crystallizable segments with low ductility, high Tg value and the tendency to form associatees". This segment arrangement is not given.
  • block copolymers with ester and amide structures which have the composition according to the invention can also be composted. However, their synthesis is significantly more complex.
  • the monomers used to prepare the copolymers can come from the following groups:
  • Dialcohols such as ethylene glycol, 1,4-butanediol, 1,3-propanediol, 1,6-hexanediol, diethylene glycol and others, and / or dicarboxylic acids such as oxalic acid, succinic acid, adipic acid and others also in the form of their respective esters (methyl, ethyl, etc .) and / or hydroxycarboxylic acids and lactones such as caprolactone and others and / or amino alcohols such as ethanolamine, propanolamine etc. and / or cyclic lactams such as epsilon-captrolactam or laurolactam etc.
  • dicarboxylic acids such as oxalic acid, succinic acid, adipic acid and others also in the form of their respective esters (methyl, ethyl, etc .) and / or hydroxycarboxylic acids and lactones such as caprolactone
  • omega-aminocarboxylic acid such as aminocaproic acid etc. and / or mixtures ( 1: 1 salts) from dicarboxylic acid such as adipic acid, succinic acid etc. and diamines such as hexamethylene diamine, diaminobutane etc.
  • both hydroxyl- or acid-terminated polyesters with molecular weights between 200 and 10,000 can be used as the ester-forming component.
  • the synthesis can be carried out either by the polyamide method by stoichiometric mixing of the starting components, optionally with the addition of water and subsequent removal of water from the reaction mixture, or by the polyester method by adding an excess of diol with esterification of the acid groups and subsequent transesterification or transamidation of these esters. In this second case, the excess glycol is distilled off in addition to water.
  • caprolactam, diol and dicarboxylic acid are preferably mixed in the desired stoichiometry for the production of polyester amides for biodegradable film components.
  • the polyester amides which can be used can furthermore contain 0.1 to 5% by weight, preferably 0.1 to 2% by weight, of branching agents.
  • branching agents can include, for example, alcohols such as trimethylolpropane or glycerol, tetrafunctional alcohols such as pentaerythritol, trifunctional carboxylic acids such as citric acid.
  • the branching agents increase the melt viscosity of the polyester amides according to the invention to such an extent that extrusion blow molding of these polymers is possible. This does not hinder the biodegradation of these materials.
  • Aliphatic polyesteramides which can be used in the context of the invention have ester fractions between 35 and 80% by weight, containing aliphatic dialcohols with a chain length of C 2 to C 12 , preferably C 2 to C 5 , aliphatic dicarboxylic acids or their esters with a chain length of C-, to C 12 , preferably C 2 to C 6 , omega-aminocarboxylic acids with a chain length of C, to C 12 , preferably C 4 to C 6 , or cyclic lactams with a ring size of C 5 to C 12 , preferably C 5 to C ⁇ , or a 1: 1 salt of aliphatic dicarboxylic acid and aliphatic diamine with a chain length of C 4 to C 12 , preferably C 4 to C 6 , with optionally 0.01 to 5% by weight, preferably 0.01 to 3 % By weight of branching. They have a melting point of more than 75 ° C and a molecular weight
  • the aliphatic polyesteramides suitable for film production can contain 0 to 50% by weight of inorganic or organic fillers or reinforcing materials, mineral fillers, UV stabilizers, antioxidants, pigments, dyes, nucleating agents, crystallization accelerators or retarders, flow aids, lubricants, Mold release agents, flame retardants and modified or unmodified rubbers.
  • inorganic or organic fillers or reinforcing materials mineral fillers, UV stabilizers, antioxidants, pigments, dyes, nucleating agents, crystallization accelerators or retarders, flow aids, lubricants, Mold release agents, flame retardants and modified or unmodified rubbers.
  • additives and auxiliaries mentioned it should preferably be ensured that the compostability of the polyester amides is essentially not adversely affected.
  • biodegradable copolyesters and their blends with starch are suitable as biodegradable goods.
  • the basic framework of biodegradable Polyesters form copolyesters from well-known aliphatic diols, aliphatic and aromatic dicarboxylic acids. All monomers used are biodegradable and ecotoxicologically harmless. The statistical incorporation of the aromatic dicarboxylic acid units is important since, in the presence of longer aromatic blocks, complete degradability is no longer achieved.
  • Copolyester and starch blends are also suitable.
  • Thermoplastic starch is first produced from native wheat, maize or potato starch and a plasticizer such as glycerin in an extruder and then processed "on line" with the copolyester to form a blend.
  • Important parameters are a complete digestion of the native starch in the extruder (i.e. destruction of the crystalline superstructures in the starch grain, but no reduction in molecular weight) and the setting of the desired blend morphology.
  • the copolyester is present as a continuous phase in which the thermoplastic starch is finely dispersed. This targeted hydrophobicization of the starch achieves the water resistance of the starch blend required for many areas of application. Films made from them show good mechanical properties such as high tear resistance and -expansion, are antistatic, permeable to oxygen and water vapor, printable, sealable and are characterized by an extremely pleasant soft handle.
  • the film layers made of biodegradable goods such as polyester amides or polyesters of the type mentioned above are in the form of a composite with a polyvinyl alcohol film. They can be laminated with this, for example using an adhesive.
  • a polyurethane prepolymer with isocyanate end groups based on diisocyanates of different reactivity can be used as the adhesive.
  • Such compounds with isocyanate groups have been known for a long time and can be converted to high polymers in a simple manner with suitable hard materials - usually polyfunctional alcohols. So their use as a sealant, as a varnish or adhesive is known.
  • polyurethane prepolymers with terminal isocyanate groups of different reactivity and polyfunctional alcohols which can be obtained by reacting 2,4-tolylene diisocyanate with polyfunctional alcohols in the ratio OH: NCO between 4 and 0.55 in a first reaction step and after the reaction of virtually all fast NCO groups with some of the OH groups present, in a second reaction step compared to the less reactive NCO groups of the 2,4-toluylene diisocyanate from reaction step one, more reactive diisocyanate in equimolar amounts or in excess to still free OH groups, if desired using customary catalysts and / or elevated temperatures.
  • a large number of polyfunctional alcohols can be used. Aliphatic alcohols with 2 to 4 hydroxyl groups per molecule are suitable in this stage. Although primary like secondary alcohols can also be used, the secondary are preferred.
  • the reaction products of low molecular weight polyfunctional alcohols with alkylene oxides with up to 4 carbon atoms can be used.
  • the reaction products of ethylene glycol, propylene glycol, of the isomeric butane ions or hexane ions with ethylene oxide, propylene oxide and / or butene oxide are suitable.
  • reaction products of trifunctional alcohols such as glycerol, trimethylolethane and / or trimethylpropane or higher functional alcohols such as, for example, pentaerythritol or sugar alcohols can also be used with the alkene oxides mentioned.
  • trifunctional alcohols such as glycerol, trimethylolethane and / or trimethylpropane or higher functional alcohols
  • pentaerythritol or sugar alcohols can also be used with the alkene oxides mentioned.
  • Particularly suitable are polyether polyols with a molecular weight of 100 to 10,000, preferably 1,000 to 5,000 and in particular polypropylene glycol.
  • polyether polyols can be produced by condensation of, for example, glycerol or pentaerythritol with elimination of water. Polyols commonly used in polyurethane chemistry continue to be formed by the polymerization of tetrahydrofuran.
  • the reaction products of polyfunctional low molecular weight alcohols such as propylene oxide are particularly suitable under conditions in which secondary hydroxyl groups are at least partially formed.
  • Other suitable polyether polyols are e.g. described in DE 2 559 759.
  • polyester polyols with a molecular weight of 200 to 10,000 can be used in the context of the invention for producing the adhesive that can be used.
  • polyester polyols can be used which are converted to 1 to by reacting low molecular weight alcohols, in particular ethylene glycol, propylene glycol, glycerol or trimethylolpropane 50 moles of caprolactone are formed.
  • suitable polyester polyols can be produced by polycondensation.
  • difunctional and / or trifunctional alcohols with a deficit of dicarboxylic acids and / or tricarboxylic acids or their reactive derivatives can be condensed to give polyester polyols.
  • Suitable dicarboxylic acids here are succinic acid and its higher homologues with up to 12 carbon atoms, furthermore unsaturated dicarboxylic acids such as maleic acid or fumaric acid and aromatic dicarboxylic acids, in particular the isomeric phthalic acids.
  • Citric acid or trimellitic acid are suitable as tricarboxylic acids.
  • Polyester polyols from the cited dicarboxylic acids and glycerol which have a residual content of secondary OH groups are particularly suitable for the purposes of the invention.
  • reaction products of 2,4-tolylene diisocyanate with polyfunctional alcohols which can be used according to the invention in the second reaction stage as a solvent or reactive diluent, it is important to maintain a certain ratio between hydroxyl groups and isocyanate groups. This results in suitable products which, after the more reactive NCO groups have reacted, still contain OH groups if the number of OH groups divided by the number of isocyanate groups is between 4 and 0.55, preferably between 1 and 0.6.
  • the second stage to produce the adhesive in the OH and NCO-functional reaction products of the first reaction stage, symmetrical, dicyclic diisocyanates are reacted with the remaining OH groups as reactive diluents.
  • the amount of the dicyclic diisocyanates based on the total amount of the diisocyanates in stages 1 and 2, is 5 to 80% by weight, preferably 5 to 60% by weight and in particular 10 to 40% by weight.
  • the molar ratio of OH groups: NCO groups expressed as the quotient of the OH groups, is divided by isocyanate groups, preferably 0.5 to 1.0, in particular 0.6 to 0.8, based on the remaining OH groups.
  • dicyclic diisocyanates it is important that the reactivity of their isocyanate groups towards hydroxyl groups is higher than that of the terminal isocyanate groups of the reactive diluent.
  • the diaryl diisocyanates are therefore primarily suitable. 4,4'-Diphenylmethane diisocyanate and / or substituted 4,4'-diphenylmethane diisocyanates are preferred.
  • the products which are preferably obtainable at temperatures between 40 and 100 ° C., have a substantially reduced proportion of free, monomeric tolylene diisocyanate but also of free, monomeric dicyclic diisocyanates.
  • the prepolymers are used over a large area at elevated temperatures, about 80 to 100 ° C., there is no nuisance caused by volatile tolylene diisocyanate.
  • Another advantage of the process products is their relatively low viscosity, which they e.g. suitable for solvent-free adhesive applications.
  • Such prepolymers were known to be suitable in bulk or as a solution in organic solvents for bonding plastics, in particular for laminating plastic foils, whereby customary hardeners, such as polyfunctional higher molecular alcohols, can be added (2-component systems) or surfaces with a defined moisture content can be glued directly with such available products, whereby film composites with high processing reliability can be obtained during heat sealing.
  • customary hardeners such as polyfunctional higher molecular alcohols
  • the polyurethane prepolymer adhesives of a multilayer film composite according to the invention have an equally good and excellent biodegradability and compostability as this is the case for the biodegradable goods consisting of polyester amides and / or polyester and the barrier layer made of polyvinyl alcohol.
  • the compostable composite multilayer film is characterized in that the films made of polyester and / or polyester amide are coextruded together with the barrier layer with the aid of an adhesion promoter based on polyether epoxides.
  • an adhesion promoter based on polyether epoxides.
  • the multilayer films according to the invention have an excellent spectrum of applicability and, at the same time, excellent biodegradability.
  • the invention also relates to a method for producing fully biodegradable and compostable multilayer films of the type mentioned at the beginning.
  • a barrier layer made of polyvinyl alcohol is provided according to the invention, to which one or more film layers or layers made of a biodegradable polyester and / or polyester amide are applied on both sides.
  • the films made of a biodegradable polyester and / or polyester amide are laminated with an adhesive based on a polyurethane prepolymer.
  • the films of polyester and / or polyester amide are coextruded with the barrier layer with the aid of an adhesion promoter based on polyether epoxides.
  • the adhesion promoter is used only in very small amounts and, moreover, polyether epoxy compounds are biodegradable, rot and compostable, so that either the small amount of polyether epoxide is ecologically essentially harmless or can be composted without problems.
  • the invention also relates to the use and the films mentioned above for packaging purposes, preferably in the food industry or detergent industry, medical hygiene purposes and in special composites.
  • the compostable composite multilayer film is a replacement for Polyolefin films are ideal for packaging purposes in the food industry.
  • their food safety is to be emphasized, their positive properties such as high transparency and tear resistance, which can be enhanced by biaxial stretching.
  • the compostable composite multilayer film according to the invention is outstandingly suitable for use in medical hygiene areas, applications in particular as an insert in diapers or sanitary napkins being considered.
  • polyolefin films it is possible to create a product that is completely decomposable more quickly than is the case with the hygiene articles previously available on the market.
  • FIG. 1 shows a schematic cross section through a first embodiment of a compostable composite multilayer film according to the invention, the individual layers which are close to one another being shown at a distance to improve clarity;
  • FIG. 2 shows a schematic cross section through a second embodiment of the compostable composite multilayer film according to the invention, the individual layers and layers firmly connected to one another in the finished film also being shown at a distance from one another here in order to simplify the illustration and improve clarity.
  • 1 denotes a compostable composite multilayer film.
  • This has a core layer or middle layer Foil layer 2 made of polyvinyl alcohol material.
  • the polyvinyl alcohol film acts as a barrier layer.
  • Layers 3 of biodegradable goods are arranged on both the front and the back of the polyvinyl alcohol film 2.
  • the layers 3 and the layers 2 are connected to one another by heat sealing.
  • FIG. 2 represents a modification of this first embodiment according to the invention.
  • reference number 1 denotes a compostable multilayer composite film according to the invention, which, however, in addition to the barrier layer 2 and the film layers 3 made of biodegradable goods, also has two layers 4.
  • the layers 4 denote adhesive materials based on polyurethane prepolymer, which are used to laminate the films 3 onto the barrier film 2.
  • the embodiments shown in the two Figures 1 and 2 each illustrate a symmetrical structure. However, modifications of this structure are possible within the scope of the invention.
  • the invention also includes an asymmetrical structure in which, for example, only one layer 3 is laminated onto a barrier layer 2. Finally, depending on requirements, further layers 3 or 2 can also be laminated onto the embodiment of FIGS. 1 or 2 by gluing or applied by hot coating. It is also conceivable to provide more than one barrier layer made of a PVOH.
  • Compostability of a film is defined as follows: The polymers and films to be tested are incubated in a liquid medium according to ASTM G22 (composition Table 1) with a mixture of microorganisms from garden compost with swirling (220 rpm) and air admission at 37 ° C. For this purpose, about 1 g of the polymer is inoculated into several cm 2 pieces in 250 ml of nutrient salt solution in 11 Erlenmeyer flasks with 2 ml of a suspension of 10 g of garden compost with 100 ml of nutrient salt solution. Coarse parts are separated from the compost suspension beforehand using a fine sieve. The dry matter (TS) content of the inoculated amount is then about 50 mg.
  • ASTM G22 composition Table 1
  • TS dry matter
  • HgCl 2 500 mg / 1
  • Other control batches contain cellulose (4 g / 1 type DP 500, Wolff, Walsrode) to check the growth with a natural substrate or are used without the addition of a C source to determine the background growth and the TS decrease in the inoculum.
  • Table 1 Composition of the nutrient solution according to ASTMG 22
  • ATP adenosine triphosphate
  • samples are not compostable which, under the above-mentioned conditions, allow a biomass growth of at most 15 mg / l within a maximum of 2 weeks.
  • the individual materials of a multilayer film according to the invention in the individual test each have good compostability according to the criteria mentioned. Fe he can be seen that in the composite the compostability the individual materials are better in themselves than in individual examinations.
  • the multilayer films according to the invention therefore have a quasi-synergistic biological compostability.
  • Comparative Example 1 Polyester amide from adipic acid, butanediol and aminocaproic acid with 45% by weight ester fraction 146 g (1 mol) of adipic acid, 90 g (1 mol) of 1,4-butanediol and 131 g (0.1 mol) of 6-aminocaproic acid are combined and heated up to 120 ° C within 30 minutes. After 2 hours at this temperature, the mixture is heated to 220 ° C. and a vacuum is applied. Finally, the mixture is polymerized with an oil pump vacuum at 220 ° C. for 4 h. A light yellow product is obtained which can be granulated. The melting point according to DSC is 125 ° C. The relative viscosity (1 g% in m-cresol at 25 ° C) is 2.2. In the biological degradation test, the material shows a microbial growth of 102 mg in 14 days.

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  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Epidemiology (AREA)
  • Materials Engineering (AREA)
  • Hematology (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Biodiversity & Conservation Biology (AREA)
  • Mechanical Engineering (AREA)
  • Laminated Bodies (AREA)

Abstract

Feuille multicouche composite (1) d'une bonne aptitude au compostage, présentant au moins une couche barrière (2) en alcool polyvinylique, sur laquelle sont appliquées, sur ses deux faces, une ou plusieurs feuilles (3) en polyester biodégradable et/ou en amide polyester, conjointement avec un adhésif ou un promoteur d'adhérence (4), soit par enduction par calandrage, soit par coextrusion ou enduction à chaud. Tous les matériaux utilisés pour la fabrication du composite sont biodégradables, en particulier aptes au pourrissement et au compostage, ledit composite présentant une bien meilleure aptitude au compostage que les matériaux considérés individuellement. Cette feuille multicouche composite peut remplacer, en tant que feuille barrière, les feuilles polyoléfiniques correspondantes, pour toutes les applications telles que les emballages ou les produits hygiéniques.
PCT/EP1997/004389 1996-08-14 1997-08-13 Feuille multicouche composite d'une bonne aptitude au compostage, son procede de fabrication et son utilisation WO1998006571A1 (fr)

Priority Applications (2)

Application Number Priority Date Filing Date Title
EP97942856A EP0918632A1 (fr) 1996-08-14 1997-08-13 Feuille multicouche composite d'une bonne aptitude au compostage, son procede de fabrication et son utilisation
AU44544/97A AU4454497A (en) 1996-08-14 1997-08-13 Easily compostable composite, multilayered foil, process for producing the same and its use

Applications Claiming Priority (2)

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DE19632799.7 1996-08-14
DE19632799A DE19632799A1 (de) 1996-08-14 1996-08-14 Gut kompostierbare Verbundmehrschichtfolie, Verfahren zu deren Herstellung sowie Verwendung derselben

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Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN100350982C (zh) * 2006-06-07 2007-11-28 北京联合大学生物化学工程学院 外科用液体敷料
DE102006024568A1 (de) * 2006-05-23 2007-12-06 Huhtamaki Forchheim Zweigniederlassung Der Huhtamaki Deutschland Gmbh & Co. Kg Verfahren zur Herstellung einer biologisch abbaubaren Kunststofffolie und Folie
EP2133199A1 (fr) * 2008-06-13 2009-12-16 AMPHENOL-TUCHEL ELECTRONICS GmbH Emballage compostable pour composants électroniques
NL2021596B1 (en) * 2018-09-10 2019-10-07 Compostable Coffee Cups Ip B V Biodegradable beverage cartridge
NL2021594B1 (en) * 2018-09-10 2019-10-07 Compostable Coffee Cups Ip B V Improved cartridge for the preparation of a beverage
CN116077708A (zh) * 2023-01-04 2023-05-09 九九三零生物技术有限公司 一种负载药物的长效防感染抗菌消毒液晶膜及其制备方法

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE19811226A1 (de) * 1998-03-18 1999-09-30 Wolff Walsrode Ag Mehrschichtige, thermoplastische Folien aus Polyesteramid und Verfahren zu deren Herstellung
EP1022127A3 (fr) * 1999-01-25 2001-08-08 Cryovac, Inc. Film barrière biodégradable pour poche d'ostomie
GB0806271D0 (en) * 2008-04-07 2008-05-14 Chemlink Specialities Ltd pakaging and method of manufacturing thereof
EP2261022B1 (fr) * 2009-06-12 2013-08-14 Flexopack S.A. Film dégradable
EP2589366A1 (fr) 2011-11-07 2013-05-08 IDT Biologika GmbH Emballage en film biodégradable pour agents biologiques oraux

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1992015454A1 (fr) * 1991-03-01 1992-09-17 Clopay Corporation Feuille polymer composite transformable en compost et son procede de production et de compostage
JPH0584874A (ja) * 1991-09-27 1993-04-06 Kuraray Co Ltd 易崩壊性多層体
JPH06142343A (ja) * 1992-11-02 1994-05-24 Aisero Kagaku Kk 風 船
EP0603876A1 (fr) * 1992-12-23 1994-06-29 Buck Werke GmbH & Co Matériau d'emballage biodégradable
JPH07285192A (ja) * 1994-04-19 1995-10-31 Dainippon Printing Co Ltd 樹脂積層体

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1992015454A1 (fr) * 1991-03-01 1992-09-17 Clopay Corporation Feuille polymer composite transformable en compost et son procede de production et de compostage
JPH0584874A (ja) * 1991-09-27 1993-04-06 Kuraray Co Ltd 易崩壊性多層体
JPH06142343A (ja) * 1992-11-02 1994-05-24 Aisero Kagaku Kk 風 船
EP0603876A1 (fr) * 1992-12-23 1994-06-29 Buck Werke GmbH & Co Matériau d'emballage biodégradable
JPH07285192A (ja) * 1994-04-19 1995-10-31 Dainippon Printing Co Ltd 樹脂積層体

Non-Patent Citations (3)

* Cited by examiner, † Cited by third party
Title
DATABASE WPI Section Ch Week 9318, Derwent World Patents Index; Class A14, AN 93-148834, XP002049011 *
PATENT ABSTRACTS OF JAPAN vol. 018, no. 451 (C - 1241) 23 August 1994 (1994-08-23) *
PATENT ABSTRACTS OF JAPAN vol. 096, no. 002 29 February 1996 (1996-02-29) *

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE102006024568A1 (de) * 2006-05-23 2007-12-06 Huhtamaki Forchheim Zweigniederlassung Der Huhtamaki Deutschland Gmbh & Co. Kg Verfahren zur Herstellung einer biologisch abbaubaren Kunststofffolie und Folie
CN100350982C (zh) * 2006-06-07 2007-11-28 北京联合大学生物化学工程学院 外科用液体敷料
EP2133199A1 (fr) * 2008-06-13 2009-12-16 AMPHENOL-TUCHEL ELECTRONICS GmbH Emballage compostable pour composants électroniques
NL2021596B1 (en) * 2018-09-10 2019-10-07 Compostable Coffee Cups Ip B V Biodegradable beverage cartridge
NL2021594B1 (en) * 2018-09-10 2019-10-07 Compostable Coffee Cups Ip B V Improved cartridge for the preparation of a beverage
CN116077708A (zh) * 2023-01-04 2023-05-09 九九三零生物技术有限公司 一种负载药物的长效防感染抗菌消毒液晶膜及其制备方法

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EP0918632A1 (fr) 1999-06-02
AU4454497A (en) 1998-03-06

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