Weldable multilayer foil
Abstract
Heat-sealable, gas-tight composite film of a polypropylene film, at least one adhesive layer, at least one gas barrier layer and heat seal layer containing an additive combination of an aliphatic amine, a thermoplastic polymer and a polydialkylsiloxane.

Term
No projected expiry on record.
- Priority
- Filed
- Granted
- Today
5 claims: 3 independent, 2 dependent
- 1PŘEDMĚT vynálezu 1. Svařovatelná vícevrstvá fólie, sestávající ze základní biaxiálně dloužené polypropylenové fólie, vrstvy zprostředkující adhezi z modifikovaného polyolefinů, vrstvy zabraňující průchodu plynu ze zmýdelněného kopolymerů ethylenu a vinylacetátu a svařovatelné vrstvy z polymerů olefinů, vyznačující se tím, že základní fólie nese alespoň na jednom povrchu případně alespoň monoaxiálně orientovanou kombinaci vrstev, která se skládá ze za horka svařovatelné vnější vrstvy z polyethylenu nebo kopolymerů obsahujícího alespoň 3 °/o hmotnosti ethylenu, vrstvy zprostředkující adhezi z modifikovaného polyolefinů, vrstvy zabraňující průchodu plynu ze zmýdelněného kopolymerů ethylenu a vinylacetátu, obsahujícího 50 až 80 molárních % vinylacetátových jednotek, které jsou alespoň z 90 % zmýdelněny, další vrstvy zprostředkující adhezi z modifikovaného polyolefinů a další svařovatelné vrstvy z polyethylenu nebo kopolymerů ethylenu obsahujícího alespoň 3 % hmotnosti ethylenu, přičemž případně za horka svařovatelná vnější vrstva a vrstva zprostředkující adhezi a/nebo další vrstva zprostředkující adhezi a další svařovatelná vrstva nebo vrstva zprostředkující adhezi a vrstva zabraňující průchodu plynu, popřípadě vrstva zabraňující průchodu plynu a další vrstva zprostředkující adhezi jsou smísením odpovídajících polymerů spojeny do jedné vrstvy a za horka svařovatelná vnější vrstva obsahuje kombinaci přísad sestávající z 0,3 až 1 % hmotnosti, výhodně 0,4 až 0,7 % hmotnosti, vztaženo na hmotnost za horka svařovatelné vnější vrstvy, alifatického aminu s 12 až 18 atomy uhlíku v řetězci, 0,1 až 0,7 % hmotnosti, výhodně 0,15 až 0,5 % hmotnosti dispergovaného, s polyethylenem nebo s kopolymerem ethylenu nesnášenlivého termoplastického polymeru s bodem měknutí v rozmezí od teploty nejvýše o 50 °C nižší do teploty nejvýše o 50 °C vyšší, než je teplota měknutí polyethylenu nebo kopolymerů ethylenu, vztaženo na hmotnost za horka svařovatelné vnější vrstvy a 0,1 až 1,2 % hmotnosti, výhodně 0,2 až 0,7 °/o hmotnosti, polydialkylsiloxanu, vztaženo na hmotnost za horka svařovatelné vnější vrstvy a základní fólie, popřípadě na svém druhém konci nese za horka svařova telnou vnější vrstvu, kombinaci za horka svařovatelné vnější vrstvy, vrstvy zprostředkující adhezi, vrstvy zabraňující průchodu plynu, další vrstvy zprostředkující adhezi a další za horka svařovatelné vrstvy, nebo vrstvy zprostředkující adhezi a vrstvu zabraňující průchodu plynu nebo vrstvu ze směsi polymerů vrstvy zprostředkující adhezi a vrstvy zabraňující průchodu plynu.
- 2Svařovatelná vícevrstvá fólie podle bodu 1, vyznačující se tím, že jako alifatický amin obsahuje N,N-bis-(hydroxy Ci až C4 alkyl )-Ci2 až Ci6-alkylamin.
- 3Svařovatelná vícevrstvá fólie podle bodů 1 a 2, vyznačující se tím, že jako nesnášenlivý termoplastický polymer obsahuje polyethylen s vysokou hustotou nebo kopolymer ethylenu a kyseliny methakrylové, jehož karboxylové skupiny jsou popřípadě alespoň zčásti ve formě soli s alkalickým kovem nebo ve formě zinečnaté soli, nebo polylaurolaktamid.
- 4Svařovatelná vícevrstvá fólie podle bodů 1 až 3, vyznačující se tím, že jako polydialkylsiloxan obsahuje polydimethylsiloxan. а. Svařovatelná vícevrstvá fólie podle bodů 1 až 4, vyznačující se tím, že vrstva zprostředkující adhezi je vytvořena z polypropylenu nebo polyethylenu, na který jsou naroubovány jednotky kyseliny maleinové, kyseliny fumarové, kyseliny itakonové nebo jejich anhydridů, esterů, amidů a imidů, nebo z kopolymeru ethylenu s kyselinou akrylovou, kyselinou methakrylovou a/nebo jejich solemi kovů a/nebo jejich alkylestery s 1 až 4 atomy uhlíku v alkylové skupině nebo z odpovídajícího roubovaného polymeru. б. Svařovatelná vícevrstvá fólie podle bodů 1 až 5, vyznačující se tím, že vrstva zabraňující průchodu plynu sestává z kopolymeru ethylenu a vinylacetátu obsahujícího 60 až 75 % molárních vinylacetátových jednotek, které jsou více než z 95 °/o zmýdelněny.
- 57. Svařovatelná vícevrstvá fólie podle bodů 1 až 6, vyznačující se tím, že za horka svařovatelná vnější vrstva a další svařovatelná vrstva a/nebo vrstva zprostředkující adhezi a další vrstva zprostředkující adhezi jsou totožné.
Independent claims5
107 paragraphs in 3 sections, as filed
The present invention relates to a sealable multilayer film which, due to its gas impermeability, is particularly suitable as a packaging film for goods which require low gas permeability and aroma protection.
The use of polyolefin sandwich films containing a weldable layer of ethylene homopolymers or copolymers as packaging films has long been known. It has also been attempted to improve the gas impermeability of such sandwich films by incorporating a layer of saponified ethylene / vinyl acetate copolymers. In DOS no. 2 For example, U.S. Patent 644,209 discloses a polypropylene sandwich film, the layers mediating adhesion of modified polyolefins, the saponified copolymers of ethylene and vinyl acetate, and optionally hot-sealable polyolefin layers. However, these sandwich films have the great disadvantage that their unsatisfactory sliding properties lead to defective weld seams at high packaging speeds due to abrasion, to defective packaging and to the packaging of the film on the machine parts of the packaging machines.
The above-mentioned drawbacks do not have a weldable multilayer film consisting of a basic biaxially stretched polypropylene film, a layer of adhesion-mediated layer of modified polyolefins, a gas barrier of a saponified ethylene-vinyl acetate copolymer and a weldable layer of olefin polymers according to the invention. the film carries at least one surface or at least a monoaxially oriented combination of layers, which consists of a hot-sealable outer layer of polyethylene or an ethylene copolymer containing at least 3% by weight of ethylene, an adhesion promoter layer of modified polyolefins, a layer preventing the passage of a saponified ethylene / vinyl acetate copolymer containing 50 to 80 mol% vinyl acetate units which are at least 90 ° / s saponified, other modified polyolefin adhesion promoter layers and other weldable layers of polyethylene or ethylene copolymer containing at least 3% by weight of ethylene, optionally with a hot-sealable outer layer and an adhesion promoter layer and / or another adhesion promoter layer and another weldable or adhesion promoter layer, and a gas barrier optionally, the gas barrier layer and the other adhesion promoter layer are combined into a single layer by mixing the corresponding polymers and the hot-sealable outer layer comprises an additive combination consisting of 0.3 to 1%, preferably 0.4 to 0.7% by weight, based on by weight of the hot-sealable outer layer of an aliphatic amine of 12 to 18 carbon atoms in the chain, 0.1 to 0.7% by weight, preferably 0.15 to 0.5% by weight, dispersed, with a polyethylene or an ethylene copolymer of an intolerable thermoplastic polymer having a softening temperature of not more than 50 ° C less than or equal to 50 ° C higher than the softening temperature of the polyethylene or ethylene copolymer based on the weight of the hot-sealable outer layer; 1 to 1.2% by weight, preferably 0.2 to 0.7% by weight, of polydialkylsiloxane based on the weight of the hot-sealable outer layer and the base film, optionally, on its second surface, it carries a hot-sealable outer layer, a combination of a hot-sealable outer layer, an adhesion-mediating layer, a gas-barrier layer, additional adhesion-mediating layer and another hot-sealable or adhesion-mediating layer and a gas-barrier layer polymer blends of the adhesion promoter layer and the gas barrier layer.
The advantage of the multilayer films according to the invention is that they represent a packaging material which, due to its excellent sliding and machine throughput, is also suitable for fast-working machines. Because of their low gas permeability, they can be used in particular for the packaging of perishable foods.
The polypropylene from which the base film is formed is preferably an iso tactical polypropylene having a density of 900 to 910 kg / m 3 with a melt flow index of from 1 to 4 g / 10 min at 230 ° C and a pressure of 218 kPa (DIN 53 735).
Homopolymers or copolymers of ethylene are used as the polymers for the weldable layer, with high density polyethylene or a random copolymer of ethylene and propylene containing at least 3% by weight of ethylene being preferred. A preferred copolymer of this type is a copolymer containing 94 to 96, preferably 95% by weight propylene and 4 to 6, preferably 5% by weight ethylene.
The density of the polymers forming the weldable layer should preferably be in the range of 895 to 960 kg / m 3 and the melt flow index should preferably be in the range of 1 to 7 g / 10 min at 190 ° C and 216 kPa. The melting point of the crystallites (measured in a polarizing microscope) should be between 125 ° C and 148 ° C, depending on the type of polymer.
Aliphatic tertiary amines, which are optionally once unsaturated, the aliphatic residue of which consists of a chain of carbon atoms containing from 12 to 18 carbon atoms and which are substituted by two hydroxyalkyl (C1-C6) groups, are used as the aliphatic amine component of the additive combination. N, N-bis (2-hydroxyethyl) - (C 12 to C 14 alkykylamines).
The thermoplastic polymer incompatible with the polymer forming the weldable layer should have a softening temperature in the range of not more than 50 ° C lower than not more than 50 ° C higher than the softening temperature of the weldable layer forming polymer and should be within the weldable forming polymer. the layer is dispersed, preferably in the form of particles having a size of 0.01 to 4 μ 4η, in particular from 0.1 to 2 µm. The dispersion of the intolerable polymer in the weldable layer is carried out by conventional methods known in the art, and thermoplastic resins such as high molecular weight polyethylene with a high density and softening point of about 129 ° C, ethylene methacrylic acid copolymer (softening temperature 90) are particularly suitable for this purpose. polylaurolactam (softening point about 130 ° C), acrylonitrile, butadiene and methacrylate copolymer (softening point about 185 ° C). Most preferred for this purpose is an ethylene-methacrylic acid copolymer, which is optionally in whole or in part in the form of alkali metal or zinc salts, and polylaurolactam.
The polydialkylsiloxane should have a viscosity of at least 0.1 to 1 kPa at 20 T. preferably, it should have a viscosity of at least 1 kPa. The most preferred substance for this purpose is polydimethylsiloxane.
The gas barrier layer is composed of an ethylene-vinyl acetate copolymer, preferably consisting of 50 to 80 mol%, most preferably 60 to 75 mol% vinyl acetate units. which are at least 90%, preferably more than 95% saponified.
The polymer viscosity limit [η] measured in a solvent mixture consisting of 85% by weight of phenol and 15% by weight of water should preferably be in the range of 0.07 to 0.17 l / g, preferably in the range of 0, 09 · to · 0.15 1 / g.
Modified polyolefins are used to make the adhesion promoter layer. Preferably, the polyolefins contain carboxyl groups such as polyethylene or polypropylene to which at least one monomer selected from the group consisting of alpha, beta-simply unsaturated dicarboxylic acids such as maleic acid, fumaric acid, itaconic acid and their anhydrides is grafted. , esters, amides and imides and, for ethylene copolymers with alpha, beta-unsaturated carboxylic acids, such as acrylic acid, methacrylic acid and / or their metal salts (Zn, Na) and / or their (C 1 to C 1) alkyl esters or corresponding graft polyolefins such as polyethylene or polypropylene or the above-described saponified copolymers onto which the monomer selected from the above described unsaturated is grafted of acids.
Particular preference is given to polyolefins, such as polypropylene, or copolymers of propylene and ethylene, containing not more than 1% by weight of grafted alpha-anhydride, a beta-simply unsaturated acid, such as maleic anhydride, or their saponified copolymers.
When the polymer of the adhesion promoter layer is processed into either a weldable layer or a gas barrier layer, the modified polyolefins are used in an amount corresponding to up to 40% by weight, preferably 25 to 30% by weight, based on the layer-forming polymers.
Using a combination of additives according to the invention, not only is it possible to obtain multilayer films with very good machine throughput and very good sliding properties, but it is even possible to omit conventional electrical pretreatment of the film, which is known to impair the sliding properties of the film. Also, there is no scratching or clouding of the film, which is due to the use of spacers based on inorganic powders. Surprisingly, there is no deterioration in film stickability, for example with tear strips, although such deterioration could be feared using polyalkylsiloxanes.
Thus, the combination of the additives of the invention could not be expected to achieve the desired improvement in sandwich films, especially when using known glidants such as saturated or unsaturated fatty acid amides as well as higher molecular weight substituted fatty acid amides with a melting point in the range from 70 to 150 ° C, such as erucic amides, oleic acid amide, fatty acid alkyldiamides and Ν, Ν-polyethoxylated fatty acid amides do not lead to a sufficient improvement in the sliding properties when used in high-speed packaging machines.
The sandwich films of the invention are of particular importance for the packaging of oxygen-sensitive foods.
The incorporation of additives into the polymers forming the weldable layer can be accomplished by mixing. The sandwich films of the present invention are produced by conventional lamination or melt extrusion techniques.
The additives are preferably added directly to the weldable layer-forming polymer, thereby avoiding expensive technology involving the production of pre-concentrates.
Furthermore, it is advantageous to apply the combination of layers to the base film at a later orientation orientation stage separately from the extrusion of the polypropylene film.
Conventional drawing techniques may be used for biaxial orientation. The longitudinal stretching is preferably carried out in a ratio of 5: 1 to 5: 1
7: 1a transverse stretching in a ratio of 7: 1 to 10: 1.
In the sandwich film according to the invention, the base polypropylene film should preferably have a thickness of 20 to 50 µm and the combination of layers should have a thickness of 2 to 6, preferably 3.5 to 5 µm. The weldable layer should have a thickness of 0.8 to 2 μΐη, preferably 1 μπι, the adhesion promoter layer should have a thickness of 0.1 to 1 μιη, preferably 0.4 to 0.6 µm, and the gas barrier layer should have a thickness of 0.2 to 1.2 μΐη, preferably 0.6 to 0.8 μπι.
The following test methods were used to evaluate the properties of the obtained films:
The course of the packaging shall be evaluated according to criteria established by staff including packaging machines such as displacement, hauling and absence of abrasion. If there are no defects in the packaging in relation to these criteria using higher packaging speeds, the film meets the requirements. An occasional failure means that the film is unsuitable. It is assumed that failures not caused by the defect of the processed film are eliminated by the optimum setting of the packaging machine carried out before testing.
The term strength of the weld seam means the force required to open it. This force is given in N and measured on test strips of 15 mm width. Test weld seams are made under defined conditions (50 N / cm<sup>2</sup>/ 0.5 s, 130 ° C, smooth jaws of the welding unit).
Antistatic behavior of the foil is determined by the so-called ash test. The ash test is performed after a certain charge of the film, which is achieved by triple wiping the film in one direction with a woolen cloth. The film is sufficiently antistatic when it does not attract cigarette ash located 3 cm away from the charged film.
Oxygen permeability measurements are made according to DIN 53 380.
Haze is measured according to ASTM D 1003-52.
The friction coefficient is determined in accordance with DIN 53 375.
Example 1
The multilayer sheet is produced as follows: for a hot-sealable outer layer, up to 98.7 percent by weight of ethylene-propylene copolymers containing 4.5% by weight of ethylene having a density of 900 kg / m 2<sup>3</sup> and a melt flow index of 5 g / 10 min at 230 ° C / 216 kPa and a crystallite melting point of 140 ° C, incorporating 0.5% by weight of N, N-bis (2-hydroxyethyl) C 12 to C 1-6 dialkylamine, 0.5% by weight of copolymer ethylene and methacrylic acid in which the carboxy groups are partially converted into the zinc salt, having a melt index of 5 g / 10 min at 190 ° C / 100 kPa and a melting point of 99 ° C and 0.3% by weight of 985 kg polydimethylsiloxane / m<sup>3</sup> at 20 ° C and a viscosity of 1 kPa. s at 20 ° C, this material is coextruded with modified polypropylene, such as a saponified copolymer containing 0.7% by weight of grafted maleic anhydride, having a melt index of 5 g / 10 min at 250 ° C and 21.6 MPa, for formation of adhesion-promoting layers, with a copolymer of ethylene and vinyl acetate containing 55 mole% vinyl acetate units, which are saponified 96%, for forming a gas barrier layer and with the aforementioned ethylene-propylene copolymer to form another weldable layer. The extruded material obtained is conventionally bonded to a polypropylene base foil with a density of 905 kg / m.<sup>3</sup>, a melt flow index of 2 g / 10 minutes at 230 ° C / 216 kPa and a softening temperature range of 160 to 166 ° C and the resulting sandwich film is stretched in the longitudinal direction at a ratio of 5: 1 and in the transverse direction at a ratio of 10: 1.
The composition of the layers and the properties of the finished film are given in the following tables.
Example 2
Multilayer films are produced as follows:
for the outer heat-sealable layer up to 90% by weight of ethylene-propylene copolymers containing 4,5% by weight of ethylene with a density of 900 kg / m<sup>3</sup>, a melt flow index of 5 g / 10 min at 230 ° C / 216 kPa and a crystallite melting point of 140 ° C incorporates 0.5% by weight of N, N-bis- (2-hydroxyethyl) -C12-C16alkylamine, 0.2% by weight polylaurolactamide having a density of 1,010 kg / m<sup>3</sup>, viscosity number (according to DIN 53 729/250) and a melting range of 176 to 180 ° C and 0.3% by weight of polydimethylsiloxane with a density of 985 kg / m<sup>3</sup> at 20 ° C and a viscosity of 1 kPa. s at 20 ° C; the material is extruded together in a conventional manner with a polypropylene base foil with a density of 905 kg / m<sup>3</sup>, a melt flow index of 2 g / 10 min at 230 ° C / 216 kPa and a softening temperature in the range of 160 to 166 ° C, and the resulting sandwich film is stretched in the longitudinal direction at 5: 1 and in the transverse direction at 10: 1.
The composition of the layers and the properties of the finished film are given in the following tables.
Example 3
The sandwich foil is produced as follows:
for the hot-sealable outer layer, up to 98.3% by weight of ethylene-propylene copolymers containing 4.5% by weight of ethylene having a density of 900 kg / m 2<sup>3</sup>, a melt flow index of 5 g / 10 min at 230 ° C / 216 kPa and a melting point of crystallites of 140 ° C treats 0.5% by weight of Ν, Ν-bis- (2-hydroxyethyl) -C 12 to C 16 -alkylamine, 0.5 % by weight of ethylene-methacrylic acid copolymers in which part of the carboxyl groups is present in the form of zinc salts, with a melt index of 5 grams / 10 min at 190 ° C / 100 kPa and a melting point of 99 ° C and 0,7% by weight of polydimethylsiloxane density 985 kg / m<sup>3</sup> at 20 ° C and a viscosity of 1 kPa. s at 20 ° C and this material is coextruded together with a modified propylene-ethylene copolymer, such as a saponified copolymer containing 0.5 weight percent of grafted maleic anhydride with a melt index of 10 g / 10 min at 250 ° C / 2.16 kPa, for layers an adhesion promoter and with a copolymer of ethylene and vinyl acetate containing 55 mole% vinyl acetate units, which are saponified 96%, for the gas barrier layer, and with the above-described propylene-ethylene copolymer, for a further weldable layer, the extrudate is conventionally bonded to a polypropylene base film of a density of 905 kg / m 2<sup>3</sup>, a melt flow index of 2 g / 10 minutes at 230 ° C / 216 kPa and a softening temperature range of 160 to 166 ° C, and the resulting sandwich film is stretched in the longitudinal direction by 5: 1 and in the transverse direction by 10: 1.
The composition of the layers and the properties of the finished film are given in the following tables.
Comparative example
The sandwich foil is produced as follows:
for the hot-sealable outer layer, up to 99.5% by weight of copolymers and ethylene containing 4.5% by weight of ethylene with a density of 900 kg / m<sup>3</sup>, a melt index of 5 g / 10 min at 230 ° C / 216 kPa and a crystallite melting point of 140 ° C incorporates 0.2% by weight of N, N-bis- (2-hydroxyethyl) -C 12 to C 16 -alkylamine and 0.3 by weight of erucic amide and this material is coextruded together with modified polypropylene, such as a saponified copolymer containing 0.3% by weight of grafted maleic anhydride with a melt index of 5 g / 10 minutes at 250<sup>C</sup>C / 216 kPa for the formation of adhesion-mediating layers, with a copolymer of ethylene and vinyl acetate containing 55 mole% of vinyl acetate units, which are saponified to 96%, to form a gas barrier, and with the above ethylene-propylene copolymer to form another weldable layer, extrudate is conventionally bonded to a polypropylene base film of a density of 905 kg / m<sup>3</sup>, a melt flow index of 2 g / 10 min at 230 ° C / 216 kPa and a softening temperature range of 160 to 166 ° C, and the resulting sandwich film is stretched in the longitudinal direction at a ratio of 5: 1 and in the transverse direction at a ratio of 10: 1.
The composition of the layers and the properties of the finished film are given in the following tables.
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Contents3
14 sheets
Sheet 1 Sheet 2 Sheet 3 Sheet 4 Sheet 5 Sheet 6 Sheet 7 Sheet 8 Sheet 9 Sheet 10 Sheet 11 Sheet 12 Sheet 13 Sheet 14
34 members in 18 offices
Priority claims3
| Document | Office | Kind | Date |
|---|---|---|---|
| 3114171 | Germany | A | |
| 813114171 | – | – | – |
| DE19813114171 | – | – | – |
Members34
| Document | Office | Kind | |
|---|---|---|---|
| FI821217A0 | Finland | A0 | |
| DK163082A | Denmark | A | |
| FI821217L | Finland | L | |
| NO820984L | Norway | L | |
| AU8213982A | Australia | A | |
| EP0062815A2 | European Patent Office (EPO) | A2 | |
| DE3114171A1 | Germany | A1 | |
| JPS57178747A | Japan | A | |
| PL235834A1 | Poland | A1 | |
| BR8201956A | Brazil | A | |
| ZA822379B | South Africa | B | |
| US4400428A | United States of America | A | |
| EP0062815A3 | European Patent Office (EPO) | A3 | |
| DD203013A5 | German Democratic Republic (until 1990) | A5 | |
| KR830009935A | Republic of Korea | A | |
| ES511263A0 | Spain | A0 | |
| ES8504420A1 | Spain | A1 | |
| CA1194664A | Canada | A | |
| AU548004B2 | Australia | B2 | |
| CS241505B2This record | Czechoslovakia (until 1993) | B2 | |
| PL137578B1 | Poland | B1 | |
| EP0062815B1 | European Patent Office (EPO) | B1 | |
| AT21857T | Austria | T | |
| ATE21857T1 | Austria | T1 | |
| DE3272973D1 | Germany | D1 | |
| NO158726B | Norway | B | |
| KR880001771B1 | Republic of Korea | B1 | |
| NO158726C | Norway | C | |
| FI77408B | Finland | B | |
| FI77408C | Finland | C | |
| MX160195A | Mexico | A | |
| JPH0249224B2 | Japan | B2 | |
| DK161502B | Denmark | B | |
| DK161502C | Denmark | C |
Numbers
- Publication, DOCDB
- 241505
- Publication, EPODOC
- CS241505
- Application
- 822456
- Application, DOCDB
- 245682
- Application, EPODOC
- CS19820002456
Titles
- English
- WELDABLE MULTILAYER FOIL
Classification
- CPC, 12
- B32B27/32
- Y10S428/91
- Y10T428/2826
- Y10T428/31667
- Y10T428/31913
- Y10T428/3192
- B32B7/12
- B32B27/08
- B32B27/306
- B32B2307/31
- B32B2307/518
- B32B2553/00
- IPC, 6
- B65D65 40
- B29D7 00
- B32B27 28
- B32B27 32
- H01H71 52
- H01H83 12