CA2182524C - Multilayer ethylene copolymer film - Google Patents
Multilayer ethylene copolymer filmInfo
- Publication number
- CA2182524C CA2182524C CA002182524A CA2182524A CA2182524C CA 2182524 C CA2182524 C CA 2182524C CA 002182524 A CA002182524 A CA 002182524A CA 2182524 A CA2182524 A CA 2182524A CA 2182524 C CA2182524 C CA 2182524C
- Authority
- CA
- Canada
- Prior art keywords
- film
- polyethylene
- density
- pouch
- ethylene
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 229920001038 ethylene copolymer Polymers 0.000 title description 9
- 239000004698 Polyethylene Substances 0.000 claims abstract description 103
- -1 polyethylene Polymers 0.000 claims abstract description 103
- 229920000573 polyethylene Polymers 0.000 claims abstract description 102
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims abstract description 63
- 239000005977 Ethylene Substances 0.000 claims abstract description 63
- 239000000155 melt Substances 0.000 claims abstract description 62
- 229920000642 polymer Polymers 0.000 claims abstract description 62
- 239000000565 sealant Substances 0.000 claims abstract description 55
- 239000000203 mixture Substances 0.000 claims abstract description 53
- 229920001577 copolymer Polymers 0.000 claims abstract description 44
- 239000004711 α-olefin Substances 0.000 claims abstract description 37
- 238000006116 polymerization reaction Methods 0.000 claims abstract description 24
- 229920005684 linear copolymer Polymers 0.000 claims abstract description 20
- 239000002685 polymerization catalyst Substances 0.000 claims abstract description 20
- 229920001903 high density polyethylene Polymers 0.000 claims abstract description 17
- 239000004700 high-density polyethylene Substances 0.000 claims abstract description 16
- 239000003054 catalyst Substances 0.000 claims description 33
- VXNZUUAINFGPBY-UHFFFAOYSA-N ethyl ethylene Natural products CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 claims description 20
- LIKMAJRDDDTEIG-UHFFFAOYSA-N 1-hexene Chemical compound CCCCC=C LIKMAJRDDDTEIG-UHFFFAOYSA-N 0.000 claims description 6
- 229920001897 terpolymer Polymers 0.000 claims description 6
- 239000000463 material Substances 0.000 abstract description 33
- 230000009969 flowable effect Effects 0.000 abstract description 22
- 238000004806 packaging method and process Methods 0.000 abstract description 11
- 235000013336 milk Nutrition 0.000 abstract description 10
- 239000008267 milk Substances 0.000 abstract description 10
- 210000004080 milk Anatomy 0.000 abstract description 10
- 239000010410 layer Substances 0.000 description 73
- 238000007789 sealing Methods 0.000 description 35
- 238000000034 method Methods 0.000 description 27
- 230000008569 process Effects 0.000 description 19
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 9
- 238000004519 manufacturing process Methods 0.000 description 8
- JGFZNNIVVJXRND-UHFFFAOYSA-N N,N-Diisopropylethylamine (DIPEA) Chemical compound CCN(C(C)C)C(C)C JGFZNNIVVJXRND-UHFFFAOYSA-N 0.000 description 7
- 239000012141 concentrate Substances 0.000 description 6
- 238000002844 melting Methods 0.000 description 6
- 230000008018 melting Effects 0.000 description 6
- 239000007788 liquid Substances 0.000 description 5
- 238000001125 extrusion Methods 0.000 description 4
- 230000006872 improvement Effects 0.000 description 4
- 229920000092 linear low density polyethylene Polymers 0.000 description 4
- 239000004707 linear low-density polyethylene Substances 0.000 description 4
- 241001263453 Rhagoletis nova Species 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 239000000470 constituent Substances 0.000 description 3
- 239000012792 core layer Substances 0.000 description 3
- 229920006262 high density polyethylene film Polymers 0.000 description 3
- 229920001684 low density polyethylene Polymers 0.000 description 3
- 239000004702 low-density polyethylene Substances 0.000 description 3
- 239000012968 metallocene catalyst Substances 0.000 description 3
- 239000004215 Carbon black (E152) Substances 0.000 description 2
- 229920000089 Cyclic olefin copolymer Polymers 0.000 description 2
- 101150071661 SLC25A20 gene Proteins 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 229910045601 alloy Inorganic materials 0.000 description 2
- 239000000956 alloy Substances 0.000 description 2
- IAQRGUVFOMOMEM-UHFFFAOYSA-N butene Natural products CC=CC IAQRGUVFOMOMEM-UHFFFAOYSA-N 0.000 description 2
- 101150102633 cact gene Proteins 0.000 description 2
- 239000002131 composite material Substances 0.000 description 2
- 238000007334 copolymerization reaction Methods 0.000 description 2
- 230000002950 deficient Effects 0.000 description 2
- 239000000945 filler Substances 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- 150000002430 hydrocarbons Chemical class 0.000 description 2
- 239000011229 interlayer Substances 0.000 description 2
- 235000013372 meat Nutrition 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 229910001120 nichrome Inorganic materials 0.000 description 2
- 229920003023 plastic Polymers 0.000 description 2
- 239000004033 plastic Substances 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 239000002356 single layer Substances 0.000 description 2
- 239000002002 slurry Substances 0.000 description 2
- 230000007928 solubilization Effects 0.000 description 2
- 238000005063 solubilization Methods 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 229920001169 thermoplastic Polymers 0.000 description 2
- 239000004416 thermosoftening plastic Substances 0.000 description 2
- 229910052723 transition metal Inorganic materials 0.000 description 2
- 150000003624 transition metals Chemical class 0.000 description 2
- KWKAKUADMBZCLK-UHFFFAOYSA-N 1-octene Chemical compound CCCCCCC=C KWKAKUADMBZCLK-UHFFFAOYSA-N 0.000 description 1
- 108010010803 Gelatin Proteins 0.000 description 1
- 229920010126 Linear Low Density Polyethylene (LLDPE) Polymers 0.000 description 1
- 239000004712 Metallocene polyethylene (PE-MC) Substances 0.000 description 1
- 239000004809 Teflon Substances 0.000 description 1
- 229920006362 Teflon® Polymers 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- 239000012963 UV stabilizer Substances 0.000 description 1
- 241001080526 Vertica Species 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- IFKWVQNWZSUEIA-UHFFFAOYSA-N but-1-ene;hex-1-ene Chemical compound CCC=C.CCCCC=C IFKWVQNWZSUEIA-UHFFFAOYSA-N 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000010961 commercial manufacture process Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 239000012967 coordination catalyst Substances 0.000 description 1
- 125000000058 cyclopentadienyl group Chemical group C1(=CC=CC1)* 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- 238000000113 differential scanning calorimetry Methods 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- ZSWFCLXCOIISFI-UHFFFAOYSA-N endo-cyclopentadiene Natural products C1C=CC=C1 ZSWFCLXCOIISFI-UHFFFAOYSA-N 0.000 description 1
- HEAMQYHBJQWOSS-UHFFFAOYSA-N ethene;oct-1-ene Chemical compound C=C.CCCCCCC=C HEAMQYHBJQWOSS-UHFFFAOYSA-N 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 235000015203 fruit juice Nutrition 0.000 description 1
- 229920000159 gelatin Polymers 0.000 description 1
- 239000008273 gelatin Substances 0.000 description 1
- 235000019322 gelatine Nutrition 0.000 description 1
- 235000011852 gelatine desserts Nutrition 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 235000020993 ground meat Nutrition 0.000 description 1
- 239000002638 heterogeneous catalyst Substances 0.000 description 1
- 229920006178 high molecular weight high density polyethylene Polymers 0.000 description 1
- 235000015243 ice cream Nutrition 0.000 description 1
- 238000009863 impact test Methods 0.000 description 1
- 235000015110 jellies Nutrition 0.000 description 1
- 235000013310 margarine Nutrition 0.000 description 1
- 239000003264 margarine Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229910001507 metal halide Inorganic materials 0.000 description 1
- 150000005309 metal halides Chemical class 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 235000014571 nuts Nutrition 0.000 description 1
- 125000002524 organometallic group Chemical group 0.000 description 1
- 235000021400 peanut butter Nutrition 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- 229920001343 polytetrafluoroethylene Polymers 0.000 description 1
- 239000004810 polytetrafluoroethylene Substances 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 235000013580 sausages Nutrition 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 238000004804 winding Methods 0.000 description 1
Classifications
-
- 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
- B32B27/32—Layered products comprising a layer of synthetic resin comprising polyolefins
-
- 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
- B32B1/00—Layered products having a non-planar shape
- B32B1/08—Tubular products
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
- C08L23/02—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L23/04—Homopolymers or copolymers of ethene
- C08L23/08—Copolymers of ethene
- C08L23/0807—Copolymers of ethene with unsaturated hydrocarbons only containing more than three carbon atoms
- C08L23/0815—Copolymers of ethene with aliphatic 1-olefins
-
- 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
- B32B2250/242—All polymers belonging to those covered by group B32B27/32
-
- 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
- B32B2323/00—Polyalkenes
- B32B2323/04—Polyethylene
-
- 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
- B32B2439/00—Containers; Receptacles
- B32B2439/70—Food packaging
-
- 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
- B32B2597/00—Tubular articles, e.g. hoses, pipes
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2205/00—Polymer mixtures characterised by other features
- C08L2205/02—Polymer mixtures characterised by other features containing two or more polymers of the same C08L -group
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
- C08L23/02—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L23/04—Homopolymers or copolymers of ethene
- C08L23/06—Polyethene
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2314/00—Polymer mixtures characterised by way of preparation
- C08L2314/06—Metallocene or single site catalysts
-
- 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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T156/00—Adhesive bonding and miscellaneous chemical manufacture
- Y10T156/10—Methods of surface bonding and/or assembly therefor
- Y10T156/1002—Methods of surface bonding and/or assembly therefor with permanent bending or reshaping or surface deformation of self sustaining lamina
- Y10T156/1007—Running or continuous length work
- Y10T156/1008—Longitudinal bending
- Y10T156/1013—Longitudinal bending and edge-joining of one piece blank to form tube
-
- 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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/13—Hollow or container type article [e.g., tube, vase, etc.]
- Y10T428/1334—Nonself-supporting tubular film or bag [e.g., pouch, envelope, packet, etc.]
-
- 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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/13—Hollow or container type article [e.g., tube, vase, etc.]
- Y10T428/1352—Polymer or resin containing [i.e., natural or synthetic]
- Y10T428/139—Open-ended, self-supporting conduit, cylinder, or tube-type article
- Y10T428/1393—Multilayer [continuous layer]
-
- 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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/28—Web or sheet containing structurally defined element or component and having an adhesive outermost layer
- Y10T428/2813—Heat or solvent activated or sealable
- Y10T428/2817—Heat sealable
- Y10T428/2826—Synthetic resin or polymer
-
- 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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/28—Web or sheet containing structurally defined element or component and having an adhesive outermost layer
- Y10T428/2852—Adhesive compositions
- Y10T428/2878—Adhesive compositions including addition polymer from unsaturated monomer
-
- 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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31855—Of addition polymer from unsaturated monomers
- Y10T428/31909—Next to second addition polymer from unsaturated monomers
- Y10T428/31913—Monoolefin polymer
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Laminated Bodies (AREA)
Abstract
A multilayer film and a pouch containing a flowable material are disclosed. The multiplayer film is made from two layers of a sealant film with an interposed layer of a polyethylene. The sealant film is made from a material comprising 10 to 100 parts by weight of a copolymer of ethylene and at least one C4-C10 alpha-olefin manufactured in a polymerization process using a single-site polymerization catalyst and from 0 to 90 parts by weight of at least one polymer selected from the group consisting of a linear copolymer of ethylene and at least one C4-C10 alpha-olephin having a density of from 0.900 to 0.930 g/cm3 and a melt index of from 0.3 to 2.0 dg/min, a high-pressure polyethylene having a density of from 0.916 to 0.930 g/cm3 and a melt index of from about 1 to 10 dg/min, and blends thereof. The polyethylene of the interposed layer is a high density polyethylene with a density of at least 0.930 g/cm3 and a melt index of less than 5 dg/min. The pouch is made from the multilayer film and has transversely sealed ends. The pouches are particularly useful in the packaging of flowable materials e.g. milk, especially using a vertical form, fill and seat apparatus.
Description
MULTILAYER ETHYLENE COPOLYMER FILM
The invention relates to ethylene copolymer film of ' improved stiffness and clarity, to multilayer ethylene copolymer film, to pouches formed from multilayer ethylene copolymer film and especially to such pouches filled with flowable materials, e.g. liquids. In particular embodiments, the pouches are made on so-called vertical form, fill and seal apparatus.
As used herein, the term "flowable material" does not include gaseous materials, but encompasses materials which are flowable under gravity or may be pumped. Such materials include liquids e.g. milk, water, fruit juice, oil; emulsions e.g. ice cream mix, soft margarine; pastes e.g. meat pastes, peanut butter; preserves e.g. jams, pie fillings, marmalade; jellies;
doughs; ground meat e.g. sausage meat; powders e.g. gelatin powders, detergents; granular solids e.g. nuts, sugar; and like materials. The invention described herein is particularly useful for flowable foods e.g. milk. In addition, as used herein "density" is determined by ASTM Procedure D1505-85, "stiffness" is understood to be tensile modulus of elasticity as measured by ASTM Procedure D882-91 (Method A) and "melt index" by ASTM Procedure D1238-90B (Condition E). The "melting point" of a polymer is measured as the peak melting point when performing differential scanning calorimetry (DSC) as described in ASTM Procedure D3417-83 (rev. 88).
Aspects of the invention relate to the packaging of flowable materials e.g. milk, in pouches using for example a so-called vertical form, fill and seal apparatus. Using such an apparatus, a flat web of synthetic thermoplastic film is unwound from a roll and formed into a continuous tube in a tube-forming section, by sealing the longitudinal edges on the film together to form a so-called lap seal or a so-called fin ., seal. The tube thus formed is pulled vertically downwards to a filling station. The tube is then collapsed across a transverse cross-section of the tube, the position of such cross-section being at a sealing device below the filling station. A
transverse heat seal is made, by the sealing device, at the SUBSTITUTE SHEET
2I ~~~~~. , collapsed portion of the tube, thus making an air-tight seal across the tube. The material being packaged enters the tube above the transverse heat seal in a continuous or intermittent manner, thereby filling the tube upwardly from the transverse heat seal. The tube is then allowed to drop a predetermined distance usually under the influence of the weight of the material in the tube. The jaws of the sealing device are closed again, thus collapsing the tube at a second transverse section, which may be at, above or below the air/material interface in the tube, depending on the nature of the material being packaged and the mode of operation of the process. The sealing device seals and severs the tube transversely at the second transverse section. The material-filled portion of the tube is now in the form of a pillow shaped pouch. Thus, the sealing device has sealed the top of the filled pouch, sealed the bottom of the next-to-be-formed pouch and separated the filled pouch from the next-to-be-formed pouch, all in one operation.
One vertical form, fill and seal apparatus of the type described above is a Prepac~ IS-6 liquid packaging apparatus.
A sealing device commonly used is a so-called impulse sealer which has a sealing element mounted in sealing jaws and electrically insulated therefrom. In operation, the sealing jaws are closed and an electrical current is caused to flow through a sealing element e.g. a wire, for a fraction of the time that the j aws are closed . The j aws remain closed while the seal forms. Once the sealing jaws are open the synthetic thermoplastic film must be able to provide a transverse seal that supports the weight of the flowable material e.g. liquid, in the next-to-be-formed pouch.
Pouches made from ethylene/butene-1 copolymer films tend to suffer from defective seals i.e. a tendency to have weak transverse end and/or longitudinal seals even though the operating conditions of the impulse sealer have been optimized.
Defective seals may lead to the phenomenon known as "leakers", in which the flowable material e.g. milk, may escape from the pouch through pinholes that develop at or close to the seal. It has been estimated that leakers account for about l-2% of the 1.3 litre milk pouch production.
U.S. 4,527_,437 of W.J. Storms, issued June 4, 1985, discloses the use of pouches of ethylene/octene-1 copolymer film in the packaging of flowable materials; the film disclosed has a stiffness of about 30 000 psi when the polymer of the film has a density of 0.920 g/cm3. That patent discloses that pouches made from the ethylene/octene-1 copolymer provide superior leaker performance, i.e.,. a lower percentage of leakers, compared with related films described above that are formed from linear E~thylene/butene-1 copolymers. Further improvements in leaker performance may be achieved using film formed from a linear ethylene copolymer manufactured using a single-site polymerization catalyst. However, certain films made from the ethylene copolymers manufactured using the single-site polymerization catalyst may have lower stiffness than the film of Storms patent. Lack of stiffness may adversely affect the runnability of the film on a form, fill and seal apparatus and gives poor stand-up properties for pouches in, for instance, a milk pitcher.
It has been found that the stiffness of film formed from polyethylene manufactured using a single-site polymerization catalyst may be increased in a manner that further improves the formation of pouches.
Drawings Figure 1 shows leaker rate for a pouch drop test.
Description of Imrentioy This invention provides for a skin of single-site catalyst films (SSC) and core 7Layer of stiffer polymer such as high density polyethylene (HI)PE). HDPE film used by itself, in the packaging industry tends to be hazy when viewed. It is desirable for such HDPE film when used in packaging to be clear, particularly when. used to make pouches for milk in order to present a desirable looking produce for consumption. It has been found that the clarity of films, made with outer skins (on either side of the: core layer) of SSC and a core layer of HPDE
films, are improved.
- 3a -More particularly, the present invention provides a pouch formed from a multi-layer film, which film has a stiffness of at least 20,000 psi (:138 MPa) and wherein said film comprises at least one single-site catalyst sealant polymer layer and at least one stiffening layer of high density polyethylene being of greater stiffness than the single-site catalyst polymer layer.
In yet another aspect, there is provided the pouch as set out above, wherein the. sealant polymer layer comprises 10 to 100 parts by weight of said copolymer of ethylene and at least one C4-Clo alpha-olefin manufactured in a single-site catalyst polymerization process and from 0-90 parts by weight of at least one polymer selected from a linear copolymer of ethylene and at least one C4-Cla alpha-olefin other than a single-site catalysed polymer, a high pressure polyethylene and blends thereof .
In another .aspect, the invention provides a pouch wherein the film comprises a multi-layer polyethylene film formed from two layers of a ~:ealant film and an interposed stiffening layer of polyethylene;r said sealant film being made from a composition comprising :10 to 100 parts by weight of a copolymer of ethylene and a.t least one C4-Clo alpha-olefin manufactured in a polymerization process using a single-site polymerization catalyst and from 0 to 90 parts by weight of at least one polymer selected from a linear copolymer of ethylene and at least one C4-Clo alpha-o:Lefin having a density of from 0.900 to 0.930 g/cm3 and a melt index of from 0.3 to 10.0 dg/min other than a single-site catalysed polymer, a high-pressure polyethylene having a density of from 0.916 to 0.930 g/cm3 and a melt index of from about 1 to 10 dg/min, and blends thereof;
said interposed :~tifferiing layer of polyethylene being of a thickness in the range of 5 to 110 ~,m and being formed from polyethylene having a density of at least 0.93 g/cm3 and a melt index of less then 5 dg/min; said multi-layer film having a thickness of from 40 to :130 ~,m.
- 3b -In another aspect, the invention provides a pouch wherein the film comprised a layer of a sealant film and a stiffening layer of polyethylene; said sealant film being made from a composition comprising 10 to 100 parts by weight of a copolymer of ethylene and at least one C4-Clo alpha-olefin manufactured in a polymerization process using a single-site polymerization catalyst and from 0 to 90 parts by weight of at least one polymer selected from a linear copolymer of ethylene and at least one C4-Clo ~~lpha-olefin having a density of from 0.900 to 0.930 g/cm3 and a melt index of from 0.3 to 10.0 dg/min other than a single-site catalysed polymer, a high-pressure polyethylene having a density of from 0.916 to 0.930 g/cm3 and a melt index of from about 1 to 10 dg/min, and blends thereof;
said stiffening layer of polyethylene being of a thickness in the range of 5 to 110 ~m and being formed from polyethylene having a density of at least 0.93 g/cm3 and a melt index of less than 5 dg/min; said mul.ti-layer film having a thickness of from 40 to 130 Vim.
In another form, the invention provides an improved process for making pouches filled with a flowable material, using a vertica:L form, fill and seal apparatus, in which process each pouch is made from a flat web of film by forming a tubular film therefrom with a longitudinal seal and subsequently flattening the tubular film at a first position and transversely heat sealing said tubular film at the flattened posit~Lon, filling the tubular film with a predetermined quantity of flowable material above said first position, flattening the tubular film above the predetermined quantity of flowable material at a second position and transversely heat. sealing said tubular film at the second position, wherein the improvement comprises forming the pouches from a flat web oi= film made from a multi-layer film comprising at least one single-site catalyst sealant polymer layer and at least one stiffening layer of high density polyethylene being of greater stiff~aess than the single-site catalyst polymer layer.
- 3c -The present invention provides for an ethylene co-polymer film having a) a sealant film comprising a copolymer of ethylene and at least one C4-Clo alpha-olefin manufactured in ~ 8224 a polymerization process using a single-site polymerization catalyst, and (b) a stiffening layer of polyethylene.
The stiffening layer of polyethylene is interposed between layers of the sealant film. The sealant film preferably has a density in the range of 0.86 to 0.94 g/cm' and a melt index of 0.2 to 10 dg/min and most preferably has a density in the range of 0.88 to 0.93 g/cm3 and a melt index of 0.3 to 5 dg/min.
The sealant film further comprises at least one polymer selected from the group comprising a linear copolymer of ethylene and at least one C4-Clo alpha-olef in, a high pressure polyethylene and blends thereof. Preferably the sealant film composition comprises 10 to 100 parts by weight of a copolymer of ethylene and at least one C4-Clo alpha-olefin manufactured in a polymerization process using a single-site polymerization catalyst and from 0 to 90 parts by weight of at least one polymer selected by the group comprising a linear copolymer of ethylene and blends thereof. In particularly preferred embodiments, the composition comprises 20-100 and especially 50-100 parts of the copolymer obtained using the single site catalyst, and therefore conversely 0-80, and especially 0-50 parts, respectively of the other polymers specified above.
The thickness of the sealant film and interposed stiffening layer of polyethylene may vary in accordance with this invention. In one embodiment of this invention, for example, the thickness of the interposed stiffening layer of polyethylene is approximately one mil (or 25 microns) and the sealant film approximately one mil (or 25 microns), while in another embodiment, the thickness of the interposed stiffening layer of polyethylene is in the range of 5 to 110 microns with the total thickness of the film being in the range of 40 to 130 microns.
Moreover, other embodiments of the invention may have the thickness of the interposed stiffening layer of polyethylene between 5 and 50 microns or between 5 to 20 microns.
Furthermore, the melt index of the interposed stiffening layer of polyethylene in other embodiments may be less than 1 dg/min.
The present invention also provides a multilayer polyethylene film formed from two layers of a sealant film and AMENDED Sf-~EET
IPEA/EP
2 ~ ~~~~,4 an interposed stiffening layer of polyethylene; said sealant film being made from a composition comprising 10 to 100 parts by weight of a copolymer of ethylene and at least one Cq-Clo alpha-olefin manufactured in a polymerization process using a single-site polymerization catalyst and from 0 to 90 parts by weight of at least one polymer selected from the group consisting of a linear copolymer of ethylene and at least one C4-Clo alpha-olefin having a density of from 0.90 to 0.930 g/cm3 and a melt index of from 0.3 to 2.0 dg/min, a high-pressure polyethylene having a density of from 0.916 to 0.930 g/cm3 and a melt index of from about 1 to 10 dg/min, and blends thereof ;
said interposed stiffening layer of polyethylene being of a thickness in the range of 5 to 110 microns and being formed from polyethylene having a density of at least 0.93 g/cm3 and a melt index of less than 5 dg/min; said laminate having a thickness of from 40 to 130 microns.
The present invention also provides a multilayer polyethylene film formed from two layers of a sealant film and an interposed stiffening layer of polyethylene; said sealant film being made from a composition comprising 10 to 100 parts by weight of a copolymer of ethylene and at least one C4-Clo alpha-olefin manufactured in a polymerization process using a single-site polymerization catalyst and from 0 to 90 parts by weight of at least one polymer selected from the group consisting of a linear copolymer of ethylene and at least one C4-Clo alpha-olefin having a density of from about 0.900 to 0.930 g/cm' and a melt index of from 0.3 to 10.0 dg/min, a high-pressure polyethylene having a density of from 0.916 to 0.930 g/cm3 and a melt index of from about 1 to 10 dg/min, and blends thereof, said sealant film being selected on the basis of providing pouches with an Mll-test value that is lower, at the same film thickness, than that for pouches made with a film of a blend of 85 parts of a linear ethylene/octene-1 copolymer having a density of about 0.920 g/cm' and a melt index of about 0.75 dg/min and 15 parts of a high pressure polyethylene having a density of about 0.918 g/cm3 and a melt index of 8.5 dg/min; said interposed stiffening layer of polyethylene being of a thickness in the range of 5 to 110 microns and being formed from polyethylene having a density of at least 0.93 g/cm3 and a melt index of less than 5 dg/min;
:a~~~oL~ s~~t-~
m~~~s~
2 r 8~~ ~
The invention relates to ethylene copolymer film of ' improved stiffness and clarity, to multilayer ethylene copolymer film, to pouches formed from multilayer ethylene copolymer film and especially to such pouches filled with flowable materials, e.g. liquids. In particular embodiments, the pouches are made on so-called vertical form, fill and seal apparatus.
As used herein, the term "flowable material" does not include gaseous materials, but encompasses materials which are flowable under gravity or may be pumped. Such materials include liquids e.g. milk, water, fruit juice, oil; emulsions e.g. ice cream mix, soft margarine; pastes e.g. meat pastes, peanut butter; preserves e.g. jams, pie fillings, marmalade; jellies;
doughs; ground meat e.g. sausage meat; powders e.g. gelatin powders, detergents; granular solids e.g. nuts, sugar; and like materials. The invention described herein is particularly useful for flowable foods e.g. milk. In addition, as used herein "density" is determined by ASTM Procedure D1505-85, "stiffness" is understood to be tensile modulus of elasticity as measured by ASTM Procedure D882-91 (Method A) and "melt index" by ASTM Procedure D1238-90B (Condition E). The "melting point" of a polymer is measured as the peak melting point when performing differential scanning calorimetry (DSC) as described in ASTM Procedure D3417-83 (rev. 88).
Aspects of the invention relate to the packaging of flowable materials e.g. milk, in pouches using for example a so-called vertical form, fill and seal apparatus. Using such an apparatus, a flat web of synthetic thermoplastic film is unwound from a roll and formed into a continuous tube in a tube-forming section, by sealing the longitudinal edges on the film together to form a so-called lap seal or a so-called fin ., seal. The tube thus formed is pulled vertically downwards to a filling station. The tube is then collapsed across a transverse cross-section of the tube, the position of such cross-section being at a sealing device below the filling station. A
transverse heat seal is made, by the sealing device, at the SUBSTITUTE SHEET
2I ~~~~~. , collapsed portion of the tube, thus making an air-tight seal across the tube. The material being packaged enters the tube above the transverse heat seal in a continuous or intermittent manner, thereby filling the tube upwardly from the transverse heat seal. The tube is then allowed to drop a predetermined distance usually under the influence of the weight of the material in the tube. The jaws of the sealing device are closed again, thus collapsing the tube at a second transverse section, which may be at, above or below the air/material interface in the tube, depending on the nature of the material being packaged and the mode of operation of the process. The sealing device seals and severs the tube transversely at the second transverse section. The material-filled portion of the tube is now in the form of a pillow shaped pouch. Thus, the sealing device has sealed the top of the filled pouch, sealed the bottom of the next-to-be-formed pouch and separated the filled pouch from the next-to-be-formed pouch, all in one operation.
One vertical form, fill and seal apparatus of the type described above is a Prepac~ IS-6 liquid packaging apparatus.
A sealing device commonly used is a so-called impulse sealer which has a sealing element mounted in sealing jaws and electrically insulated therefrom. In operation, the sealing jaws are closed and an electrical current is caused to flow through a sealing element e.g. a wire, for a fraction of the time that the j aws are closed . The j aws remain closed while the seal forms. Once the sealing jaws are open the synthetic thermoplastic film must be able to provide a transverse seal that supports the weight of the flowable material e.g. liquid, in the next-to-be-formed pouch.
Pouches made from ethylene/butene-1 copolymer films tend to suffer from defective seals i.e. a tendency to have weak transverse end and/or longitudinal seals even though the operating conditions of the impulse sealer have been optimized.
Defective seals may lead to the phenomenon known as "leakers", in which the flowable material e.g. milk, may escape from the pouch through pinholes that develop at or close to the seal. It has been estimated that leakers account for about l-2% of the 1.3 litre milk pouch production.
U.S. 4,527_,437 of W.J. Storms, issued June 4, 1985, discloses the use of pouches of ethylene/octene-1 copolymer film in the packaging of flowable materials; the film disclosed has a stiffness of about 30 000 psi when the polymer of the film has a density of 0.920 g/cm3. That patent discloses that pouches made from the ethylene/octene-1 copolymer provide superior leaker performance, i.e.,. a lower percentage of leakers, compared with related films described above that are formed from linear E~thylene/butene-1 copolymers. Further improvements in leaker performance may be achieved using film formed from a linear ethylene copolymer manufactured using a single-site polymerization catalyst. However, certain films made from the ethylene copolymers manufactured using the single-site polymerization catalyst may have lower stiffness than the film of Storms patent. Lack of stiffness may adversely affect the runnability of the film on a form, fill and seal apparatus and gives poor stand-up properties for pouches in, for instance, a milk pitcher.
It has been found that the stiffness of film formed from polyethylene manufactured using a single-site polymerization catalyst may be increased in a manner that further improves the formation of pouches.
Drawings Figure 1 shows leaker rate for a pouch drop test.
Description of Imrentioy This invention provides for a skin of single-site catalyst films (SSC) and core 7Layer of stiffer polymer such as high density polyethylene (HI)PE). HDPE film used by itself, in the packaging industry tends to be hazy when viewed. It is desirable for such HDPE film when used in packaging to be clear, particularly when. used to make pouches for milk in order to present a desirable looking produce for consumption. It has been found that the clarity of films, made with outer skins (on either side of the: core layer) of SSC and a core layer of HPDE
films, are improved.
- 3a -More particularly, the present invention provides a pouch formed from a multi-layer film, which film has a stiffness of at least 20,000 psi (:138 MPa) and wherein said film comprises at least one single-site catalyst sealant polymer layer and at least one stiffening layer of high density polyethylene being of greater stiffness than the single-site catalyst polymer layer.
In yet another aspect, there is provided the pouch as set out above, wherein the. sealant polymer layer comprises 10 to 100 parts by weight of said copolymer of ethylene and at least one C4-Clo alpha-olefin manufactured in a single-site catalyst polymerization process and from 0-90 parts by weight of at least one polymer selected from a linear copolymer of ethylene and at least one C4-Cla alpha-olefin other than a single-site catalysed polymer, a high pressure polyethylene and blends thereof .
In another .aspect, the invention provides a pouch wherein the film comprises a multi-layer polyethylene film formed from two layers of a ~:ealant film and an interposed stiffening layer of polyethylene;r said sealant film being made from a composition comprising :10 to 100 parts by weight of a copolymer of ethylene and a.t least one C4-Clo alpha-olefin manufactured in a polymerization process using a single-site polymerization catalyst and from 0 to 90 parts by weight of at least one polymer selected from a linear copolymer of ethylene and at least one C4-Clo alpha-o:Lefin having a density of from 0.900 to 0.930 g/cm3 and a melt index of from 0.3 to 10.0 dg/min other than a single-site catalysed polymer, a high-pressure polyethylene having a density of from 0.916 to 0.930 g/cm3 and a melt index of from about 1 to 10 dg/min, and blends thereof;
said interposed :~tifferiing layer of polyethylene being of a thickness in the range of 5 to 110 ~,m and being formed from polyethylene having a density of at least 0.93 g/cm3 and a melt index of less then 5 dg/min; said multi-layer film having a thickness of from 40 to :130 ~,m.
- 3b -In another aspect, the invention provides a pouch wherein the film comprised a layer of a sealant film and a stiffening layer of polyethylene; said sealant film being made from a composition comprising 10 to 100 parts by weight of a copolymer of ethylene and at least one C4-Clo alpha-olefin manufactured in a polymerization process using a single-site polymerization catalyst and from 0 to 90 parts by weight of at least one polymer selected from a linear copolymer of ethylene and at least one C4-Clo ~~lpha-olefin having a density of from 0.900 to 0.930 g/cm3 and a melt index of from 0.3 to 10.0 dg/min other than a single-site catalysed polymer, a high-pressure polyethylene having a density of from 0.916 to 0.930 g/cm3 and a melt index of from about 1 to 10 dg/min, and blends thereof;
said stiffening layer of polyethylene being of a thickness in the range of 5 to 110 ~m and being formed from polyethylene having a density of at least 0.93 g/cm3 and a melt index of less than 5 dg/min; said mul.ti-layer film having a thickness of from 40 to 130 Vim.
In another form, the invention provides an improved process for making pouches filled with a flowable material, using a vertica:L form, fill and seal apparatus, in which process each pouch is made from a flat web of film by forming a tubular film therefrom with a longitudinal seal and subsequently flattening the tubular film at a first position and transversely heat sealing said tubular film at the flattened posit~Lon, filling the tubular film with a predetermined quantity of flowable material above said first position, flattening the tubular film above the predetermined quantity of flowable material at a second position and transversely heat. sealing said tubular film at the second position, wherein the improvement comprises forming the pouches from a flat web oi= film made from a multi-layer film comprising at least one single-site catalyst sealant polymer layer and at least one stiffening layer of high density polyethylene being of greater stiff~aess than the single-site catalyst polymer layer.
- 3c -The present invention provides for an ethylene co-polymer film having a) a sealant film comprising a copolymer of ethylene and at least one C4-Clo alpha-olefin manufactured in ~ 8224 a polymerization process using a single-site polymerization catalyst, and (b) a stiffening layer of polyethylene.
The stiffening layer of polyethylene is interposed between layers of the sealant film. The sealant film preferably has a density in the range of 0.86 to 0.94 g/cm' and a melt index of 0.2 to 10 dg/min and most preferably has a density in the range of 0.88 to 0.93 g/cm3 and a melt index of 0.3 to 5 dg/min.
The sealant film further comprises at least one polymer selected from the group comprising a linear copolymer of ethylene and at least one C4-Clo alpha-olef in, a high pressure polyethylene and blends thereof. Preferably the sealant film composition comprises 10 to 100 parts by weight of a copolymer of ethylene and at least one C4-Clo alpha-olefin manufactured in a polymerization process using a single-site polymerization catalyst and from 0 to 90 parts by weight of at least one polymer selected by the group comprising a linear copolymer of ethylene and blends thereof. In particularly preferred embodiments, the composition comprises 20-100 and especially 50-100 parts of the copolymer obtained using the single site catalyst, and therefore conversely 0-80, and especially 0-50 parts, respectively of the other polymers specified above.
The thickness of the sealant film and interposed stiffening layer of polyethylene may vary in accordance with this invention. In one embodiment of this invention, for example, the thickness of the interposed stiffening layer of polyethylene is approximately one mil (or 25 microns) and the sealant film approximately one mil (or 25 microns), while in another embodiment, the thickness of the interposed stiffening layer of polyethylene is in the range of 5 to 110 microns with the total thickness of the film being in the range of 40 to 130 microns.
Moreover, other embodiments of the invention may have the thickness of the interposed stiffening layer of polyethylene between 5 and 50 microns or between 5 to 20 microns.
Furthermore, the melt index of the interposed stiffening layer of polyethylene in other embodiments may be less than 1 dg/min.
The present invention also provides a multilayer polyethylene film formed from two layers of a sealant film and AMENDED Sf-~EET
IPEA/EP
2 ~ ~~~~,4 an interposed stiffening layer of polyethylene; said sealant film being made from a composition comprising 10 to 100 parts by weight of a copolymer of ethylene and at least one Cq-Clo alpha-olefin manufactured in a polymerization process using a single-site polymerization catalyst and from 0 to 90 parts by weight of at least one polymer selected from the group consisting of a linear copolymer of ethylene and at least one C4-Clo alpha-olefin having a density of from 0.90 to 0.930 g/cm3 and a melt index of from 0.3 to 2.0 dg/min, a high-pressure polyethylene having a density of from 0.916 to 0.930 g/cm3 and a melt index of from about 1 to 10 dg/min, and blends thereof ;
said interposed stiffening layer of polyethylene being of a thickness in the range of 5 to 110 microns and being formed from polyethylene having a density of at least 0.93 g/cm3 and a melt index of less than 5 dg/min; said laminate having a thickness of from 40 to 130 microns.
The present invention also provides a multilayer polyethylene film formed from two layers of a sealant film and an interposed stiffening layer of polyethylene; said sealant film being made from a composition comprising 10 to 100 parts by weight of a copolymer of ethylene and at least one C4-Clo alpha-olefin manufactured in a polymerization process using a single-site polymerization catalyst and from 0 to 90 parts by weight of at least one polymer selected from the group consisting of a linear copolymer of ethylene and at least one C4-Clo alpha-olefin having a density of from about 0.900 to 0.930 g/cm' and a melt index of from 0.3 to 10.0 dg/min, a high-pressure polyethylene having a density of from 0.916 to 0.930 g/cm3 and a melt index of from about 1 to 10 dg/min, and blends thereof, said sealant film being selected on the basis of providing pouches with an Mll-test value that is lower, at the same film thickness, than that for pouches made with a film of a blend of 85 parts of a linear ethylene/octene-1 copolymer having a density of about 0.920 g/cm' and a melt index of about 0.75 dg/min and 15 parts of a high pressure polyethylene having a density of about 0.918 g/cm3 and a melt index of 8.5 dg/min; said interposed stiffening layer of polyethylene being of a thickness in the range of 5 to 110 microns and being formed from polyethylene having a density of at least 0.93 g/cm3 and a melt index of less than 5 dg/min;
:a~~~oL~ s~~t-~
m~~~s~
2 r 8~~ ~
said laminate having a thickness of from 40 to 130 microns.
The M11 test is described below.
The present invention further provides a multilayer polyethylene film formed from a layer of a sealant film and a stiffening layer of polyethylene; said sealant film being made from a composition comprising 10 to 100 parts by weight of a copolymer of ethylene and at least one Cq-Clo alpha-olefin manufactured in a polymerization process using a single-site polymerization catalyst and from 0 to 90 parts by weight of at least one polymer selected from the group consisting of a linear copolymer of ethylene and at least one C4-Clo alpha-olefin having a density of from 0.900 to 0.930 g/cm3 and a melt index of from 0.3 to 2.0 dg/min, a high-pressure polyethylene having a density of from 0.916 to 0.930 g/cm' and a melt index of from about 1 to 10 dg/min, and blends thereof;
said stiffening layer of polyethylene being of a thickness in the range of 5 to 110 microns and being formed from polyethylene having a density of at least 0.93 g/cm3 and a melt index of less than 5 dg/min; said multilayer film having a thickness of from 40 to 130 microns.
The present invention additionally provides a film formed from two layers of a sealant film and an interposed stiffening layer of a film having a higher stiffness than the sealant layer, said layer of higher stiffness being formed from a polymer having a melting point of not more than 140°C; said sealant film being made from a composition comprising 10 to 100 parts by weight of a copolymer of ethylene and at least one C4-Clo alpha-olefin manufactured in a polymerization process using a single-site polymerization catalyst and from 0 to 90 parts by weight of at least one polymer selected from the group consisting of a linear copolymer of ethylene and at least one C4-Clo alpha-olefin having a density of from 0.900 to 0.930 g/cm' and a melt index of from 0.3 to 2.0 dg/min, a high-pressure polyethylene having a density of from 0.916 to 0.930 g/cm3 and a melt index of from about 1 to 10 dg/min, and blends thereof; said interposed stiffening layer of higher stiffness being of a thickness in the range of 5 to 110 microns and being formed from polyethylene having a density of at least 0.93 g/cm3 and a melt index of less than 5 dg/min;
said laminate having a thickness of from 40 to 130 microns.
pN~Ef~IDcD SHEET
lPEAIFP
2 G ~25Z4 _ 7 _ The present invention also provides a multilayer film formed from a layer of a sealant film and a layer of a film having a higher stiffness than the sealant layer, said layer of higher stiffness being formed from a polymer having a melting point of not more than 140°C; said sealant film being made from a composition comprising 10 to 100 parts by weight of a copolymer of ethylene and at least one C4-Clo alpha-olefin manufactured in a polymerization process using a single-site polymerization catalyst and from 0 to 90 parts by weight of at least one polymer selected from the group consisting of a linear copolymer of ethylene and at least one C4-Clo alpha-olefin having a density of from 0.900 to 0.930 g/cm3 and a melt index of from 0.3 to 2.0 dg/min, a high-pressure polyethylene having a density of from 0.916 to 0.930 g/cm' and a melt index of from about 1 to 10 dg/min, and blends thereof;
said layer of higher stiffness being of a thickness in the range of 5 to 110 microns; said multilayer film having a thickness of from 40 to 130 microns.
In preferred embodiments of the multilayer film of the present invention, the film has a stiffness of at least 20 000 psi (=135 Mpa) , and especially at least 25 000 psi (=170 Mpa) .
The present invention also provides a pouch containing a flowable material, said pouch being made from a multilayer film in tubular form and having transversely heat sealed ends, said multilayer polyethylene film being formed from two layers of a sealant film and an interposed stiffening layer of polyethylene; said sealant film being made from a composition comprising 10 to 100 parts by weight of a copolymer of ethylene and at least one C4-Clo alpha-olefin manufactured in a polymerization process using a single-site polymerization catalyst and from 0 to 90 parts by weight of at least one polymer selected from the group consisting of a linear copolymer of ethylene and at least one C4-Clo alpha-olefin having a density of from 0.900 to 0.930 g/cm3 and a melt index of from 0.3 to 2.0 dg/min, a high-pressure polyethylene having a density of from 0.916 to 0.930 g/cm' and a melt index of f rom about 1 to 10 dg/min, and blends thereof ; said interposed stiffening layer of polyethylene being of a thickness in the range of 5 to 110 microns and being formed from polyethylene having a density of at least 0.93 g/cm' and a melt index of Ai~ENaED SHEET
IPEA/EP
_$-less than 5 dg/min; said multilayer film having a thickness of from 40 to 130 microns.
The present invention also provides a pouch for containing a flowable material, said pouch being made from a multilayer film in tubular form and having transversely heat sealed ends, said multilayer polyethylene film being formed from two layers of a sealant film and an interposed stiffening layer of polyethylene; said sealant film being made from a composition comprising 10 to 100 parts by weight of a copolymer of ethylene and at least one C4-Clo alpha-olefin manufactured in a polymerization process using a single-site polymerization catalyst and from 0 to 90 parts by weight of at least one polymer selected from the group consisting of a linear copolymer of ethylene and at least one C4-Clo alpha-olefin having a density of from 0.900 to 0.930 g/cm3 and a melt index of from 0.3 to 10.0 dg/min, a high-pressure polyethylene having a density of from 0.916 to 0.930 g/cm3 and a melt index of from about 1 to 10 dg/min, and blends thereof, said sealant film being selected on the basis of providing pouches with an M11-test value that is lower, at the same film thickness, than that for pouches made with a film of a blend of 85 parts of a linear ethylene/octene-1 copolymer having a density of about 0.920 g/cm3 and a melt index of about 0.75 dg/min and 15 parts of a high-pressure polyethylene having a density of about 0.918 g/cm3 and a melt index of 8.5 dg/min;
said interposed stiffening layer of polyethylene being of a thickness in the range of 5 to 110 microns and being from from polyethylene having a density of at least 0.93 g/cm3 and a melt index of less than 5 dg/min; said multilayer film having a thickness of from 40 to 130 microns.
In a preferred embodiment of the laminate and pouches of the present invention, the copolymer made with a single-site catalyst has a density in the range of 0.8-0.93 g/cm3 especially in the range of 0.88 to 0.91 g/cm3; and a melt index of less than 5 dg/min particularly in the range of 0.3 to 2 dg/min, and especially in the range of 0.5 to 1.5 dg/min.
In a further embodiment, the copolymer made with a single-site catalyst is an ethylene/butene-1 copolymer, an ethylene/hexene-1 copolymer, ethylene/octene-1 copolymer, ethylene/hexene-1/butene-1 terpolymer or an ethylene/octene 1/butene-1 terpolymer.
Adv~~~t~~~ ~~iEt'~
~PEA/Et~
2162~a24 _ g _ The present invention further provides a process for making pouches filled with a flowable material, using a vertical form, fill and seal apparatus, in which process each pouch is made from a flat web of film by forming a tubular film therefrom with a longitudinal seal and subsequently flattening the tubular film at a first position and transversely heat sealing said tubular film at the flattened position, filling the tubular film with a predetermined quantity of flowable material above said first position, flattening the tubular film above the predetermined quantity of flowable material at a second position and transversely heat sealing said tubular film at the second position, the improvement comprising making the pouches from a flat web of a film made from a multilayer film formed from two layers of a sealant film and an interposed stiffening layer of polyethylene; said sealant film being made from a composition comprising 10 to 100 parts by weight of a copolymer of ethylene and at least one C4-Clo alpha-olefin manufactured in a polymerization process using a single-site polymerization catalyst and from 0 to 90 parts by weight of at least one polymer selected from the group consisting of a linear copolymer of ethylene and at least one C4-Clo alpha-olefin having a density of from 0.900 to 0.930 g/cm' and a melt index of from 0.3 to 2.0 dg/min, a high-pressure polyethylene having a density of from 0.916 to 0.930 g/cm' and a melt index of from about 1 to 10 dg/min, and blends thereof ; said interposed stiffening layer of polyethylene being of a thickness in the range of 5 to 110 microns and being formed from polyethylene having a density of at least 0.93 g/cm3 and a melt index of less than 5 dg/min; said multilayer film having a thickness of from 50 to 100 microns.
The present invention also provides, in a process for making pouches filled with a flowable material, using a vertical form, fill and seal apparatus, in which process each pouch is made from a flat web of film by forming a tubular film therefrom with a longitudinal seal and subsequently flattening the tubular film at a first position and transversely heat sealing said tubular film at the flattened position, filling the tubular film with a predetermined quantity of flowable material above said first position, flattening the tubular film above the predetermined quantity AMENDED SHEET
tPEA/EP
2 l 8~~ 2 -la-of flowable material at a second position and transversely heat sealing said tubular film at the second position, the improvement comprising making the pouches from a flat web of film made from a composite formed from two layers of a sealant film and an interposed stiffening layer of polyethylene; said sealant film being made from a composition comprising 10 to 100 parts by weight of a copolymer of ethylene and at least one C4-Clo alpha-olefin manufactured in a polymerization process using a single-site polymerization catalyst and from 0 to 90 parts by weight of at least one polymer selected from the group consisting of a linear copolymer of ethylene and at least one C4-Clo alpha-olefin having a density of from 0.900 to 0.930 g/cm3 and a melt index of from 0.3 to 10.0 dg/min, a high-pressure polyethylene having a density of from 0.916 to 0.930 g/cm3 and a melt index of from about 1 to 10 dg/min, and blends thereof, said sealant film being selected on the basis of providing pouches with an Mll-test value that is lower, at the same film thickness, than that for pouches made with a film of a blend of 85 parts of a linear ethylene/octene-1 copolymer having a density of about 0.920 g/cm' and a melt index of about 0.75 dg/min and 15 parts of a high-pressure polyethylene having a density of about 0.918 g/cm' and a melt index of 8.5 dg/min.
Although melt index ranges are specified herein, it is understood that the polymers have melt indices typical of film-grade polymers.
Although the invention may be a multilayer film of a sealant film and another layer, especially polyethylene, and the related pouches and process described herein, the invention will be particularly described with reference to a multilayer or composite of two layers of sealant film and an interposed stiffening layer of polyethylene film. The latter multilayer films are preferred because of the ability to form a lap seal as well as a fin seal and the substantial absence of curl in the laminate. In addition, although the non-sealant layer may be a lyer of higher stiffness formed from a polymer having a melting point of not more than 140°C, that layer will be particularly described herein with reference to a layer of polyethylene.
The multilayer film is made, in part, from a composition comprising 10 to 100 parts by weight of a copolymer of a ,AMENDED SHEET
IPEA/EP
2 ~ 8 2524 copolymer of ethylene and at least one Cq-Clo alpha-olefin manufactured in a polymerization process using a single-site polymerization catalyst and from 0 to 90 parts by weight of at least one polymer selected from the group consisting of a linear copolymer of ethylene and at least one CQ-Clo alpha-olefin having a density of from 0.900 to 0.930 g/cm' and a melt index of from 0.3 to 2.0 dg/min, a high-pressure polyethylene having a density of from 0.916 to 0.924 g/cm3 and a melt index of from about 1 to 10 dg/min, and blends thereof .
In embodiments, the composition comprises 20-100 and especially 50-100 parts of the copolymer obtained using the single site catalyst, and conversely 0-80 and 0-50 parts of the other polymer specified above.
The polyethylene of the interlayer may be a so-called high-pressure polyethylene or a so-called linear polyethylene, and blends thereof. In embodiments, the polyethylene is 0 100% by weight of a high density polyethylene, including high molecular weight high density polyethylene, preferabloy 20 100% by weight of such polyethylene and in particular 75-100%
by weight of such polyethylene. The remainder of the polyethylene, if any, i.e., 0-80% by weight and especially 0-250 by weight, is a linear polyethylene or a recycled polyethylene obtained from any of a variety of sources provided that the recycled polyethylene meets the appropriate governmental or other regulations for packaging of the material that is to be packaged. The composition used for the interlayer (stiffening) needs to meet the density and melt index values specified herein viz. be a polyethylene having a density of at least 0.93 g/cm3 and a melt index of less than 1 dg/min.
Processes for the manufacture of so-called high pressure polyethylene from ethylene monomer have been operated commercially for decades. A variety of such polymers are available. The high pressure polyethylene of the sealant layer has a density of 0.916 to 0.930 g/cm3, especially 0.918 to 0.925 g/cm3. In addition, the high pressure polyethylene has a melt index in the range of 1 to 10 dg/min. and especially in the range of 0.5 to 5 dg/min. For the interposed layer, the high pressure polyethylene would have a density and melt index in the range described herein.
,~Nl~~;~~~ ~~iEE~
I~EA/E~' 2(8~5Z~
Processes for the commercial manufacture of linear polyethylene have been known for more than thirty years . Such processes may be operated at temperature above the solubilization temperature of the polymer in which event the polymer remains in solution, or the processes may be operated below the solubilization temperature in which event the polymer remains as a slurry in the polymerization solvent.
Processes are also known in which the polymerization is conducted in the gas phase in the absence of solvent. Other processes operate at both high temperature and high pressure.
The catalysts used are frequently based on titanium and are referred to as coordination catalysts; such catalysts may also be described as multi-site catalysts or heterogeneous catalysts. The polymer obtained is linear in nature, as opposed to the branched nature of high pressure polyethylene.
Linear low density polyethylene AMENDED SHEET
IPEA/EP
t WO 95/21743 ~ 2,,~( PCT/CA95/00064 is obtained by the co-polymerization of ethylene with at least one C9-Clo alpha-olefin hydrocarbon comonomer, examples of which include butene-1, hexene-1 and octene-1. The linear low density polyethylene has a density in the range of 0.900 to 0.930 g/cm3, preferably 0.912 to 0.930 g/cm3 and especially in the range of 0.918 to 0.925 g/cm3. In addition the polymer has a melt index in the range of 0.3 to 10.0 dg/min, preferably 0.3 to 2.0 dg/min and especially in the range of 0.5 to 1.5 dg/min.
The high density polyethylene has a density of at least 0.930 g/cm', especially in the range of 0.935-0.965 g/cm3.
Similarly, the high density polyethylene has a melt index of less than 1 dg/min and especially in the range of 0.01 to 0.3 dg/min; polymer in the lower end of that range may be classified as high molecular weight polyethylenes. The high density polyethylene may be high pressure polyethylene or linear polyethylene.
The ethylene copolymer made with single-site catalyst may be obtained using a variety of polymerization processes of the type described above for the manufacture of linear low density polyethylene e.g. processes that operate in solution, in the gas phase and as a slurry process; references to the use of single site catalysts in polymerization processes is made in Modern Plastics, p.15, May 1993, Plastics Focus Vol. 25, No.
12, June 21, 1993 and in Exxon Chemical Exact Facts, Vol.l, No.
1, February 1993. Such polymers are obtained by the co-polymerization of ethylene with at least one C4-Clo alpha-olefin hydrocarbon comonomer, examples of which include butene-1, hexene-1 and octene-1. The catalyst used is a so-called single-site catalyst, certain of which may also be referred to as metallocene or constrained geometry catalysts.
By the term "single-site catalyst" is meant a metallocene or constrained geometry catalyst. Metallocene catalysts are organometallic co-ordination compounds obtained as a cyclopentadienyl (Cp) derivative of a transition metal or metal halide. The metal is bonded to the Cp ring by electrons moving in orbitals extending above and below the plane of the ring (pi bond). Metallocene catalysts systems are extremely sensitive 2 I ~2~2~
to the geometry of the catalytic site at the transition metal (the "single-site"). Examples of single-site catalysts include CpzTICl2, Cp2ZrClz, CpzHfClZ, (CS (CH3) z) aTiCl2, PHZMe (Ind) ZZrCl2, (Me4Cpsi (Me) 2N(t-Bu) ] TiCHz [o-PhN (Mez) ] , Cp2Fe B (C2F2,4_ The polyethylene obtained with the single site catalyst preferably has a density in the range of 0.8 to 0.93 g/cm3, moreover in the range of 0.88 to 0.930 g/cm', and specially in the range of 0.89 to 0.910 g/cm'. In addition the polymer preferably has a melt index of less than 5 dg/min, particularly in the range of 0.3 to 2.0 dg/min and especially in the range of 0.5 to 1.5 dg/min. Preferred polymers include ethylene/butene-1, ethylene/hexene-1, ethylene/octene-1 and ethylene/hexene-1/butene-1 terpolymers.
The multilayer polyethylene film in one embodiment has a thickness of 40 to 130 microns, and especially in the range of 50 to 100 microns. In particular embodiments e.g. for use on a form, fill and seal apparatus, the laminate thickness is preferably in the range of 50 to 70 microns. The sealant layers on opposed sides of the interposed polyethylene layer are preferably of substantially equal thickness, although this is not essential provided that the requirements for the intended end-use are met, to allow the film to be reversed and/or opposing sides to be bonded together as in a tube. The interposed layer has a thickness of 5 to 110 microns, in one embodiment 5 to 50 microns and especially 8 to 16 microns in other embodiments.
The M11-test is as follows: In general terms, the M11-test is a drop test carried out on 1.3 litre water-filled pouches.
In the test, pouches containing 1.3 litres of water, at a temperature of 10~5'C, are made from a 32 cm. wide film web, on a Prepac IS-6 vertical form, fill and seal apparatus. The web of film is formed into a continuous tube with a lap seal, said tube having an inside diameter of approximately 9.8 cm. A
typical vertical sealing jaw of the Prepac IS-6 apparatus has an approximately 3.5 by 0.3 mm rectangular sealing wire made of Nichrome° alloy, and a transverse sealing jaw with an approximately 1.8 by 0.7 mm sealing wire made of Nichrome°
AMENDED Si~EET
IPEA/EP
WO 95/21743 ~ ~,a' PCT/CA95/00064 alloy. The operation of the vertical and transverse sealing element should be optimized for the particular film type and thickness used. Typically, during vertical sealing of the tube, a 35-50 amp current at 14-24 volts is passed through the sealing wire for about 0.2-0.5 seconds. The force applied by the vertical sealing jaws to the film is about 8 N applied for a dwell time of about 0.9 seconds. The vertical sealing jaw is cooled by water at 13'~6'C. During transverse sealing of the tube, a 35-55 amp current at 10-15 volts is passed through the sealing wire for about 0.2-0.5 seconds. The force applied by the transverse sealing jaws to the film is about 19 N applied for a dwell time of about 0.9 seconds. The transverse sealing jaw is cooled by water at 13'~6'C. Both sealing jaws are covered with 150 ~,m thick glass f fiber tape impregnated with Teflon° polytetrafluoroethylene resin. With respect to optimizing the sealing operations, it will be recognized that the sealing conditions (e. g. amperage, voltage, dwell time) depend on the gauge and melting characteristics of the film.
For example, a 50~Cm film would require lower amperage and voltage, as controlled by the rheostat on the apparatus, than would a 75~m film. Typically such a change in film thickness requires an adjustment of approximately 10% of the rheostat range.
The water-filled pouches containing the cold water, are dropped onto a concrete floor from a height of 335 cm. The pouches are positioned with the longitudinal axis of the tube i.e. pouch, coincident with an imaginary vertical line.
Any pouch from which water flows or weeps after the pouch has been dropped onto the floor, is termed a "leaker". The number of leakers, expressed as a percentage of the total number of pouches dropped is the M11-test value for the particular film being tested. It will be noted that the M11-test value will be affected by the thickness of the film as well as the material from which the film is made.
As noted above, it is the sealant film that is selected upon the basis of a drop test such as the M11-test. It is to be WO 95/21743 '~~ ~~ PCT/CA95/00064 understood, therefore, that pouches made with other pouch-forming apparatus come within the scope of the present invention.
The blends useful in the present invention may be made by blending the constituents prior to feeding to the hopper of a film extruder, or may be made by blending the constituents at the time of extrusion just prior to remelting in the extruder, or alternatively the constituents may be melt blended in the extruder.
The ethylene/a-olefin copolymer or blend of ethylene/a-olefin copolymer e.g. in pellet form, may be fed into a film extruder and extruded into film form using known techniques.
One preferred method of manufacturing film is the so-called blown film process disclosed in Canadian Patent No. 460 963 issued November S, 1949 to E.D. Fuller. Another preferred method of manufacturing film uses an internal or external cooling mandrel in the blown film process, as disclosed for example in Canadian Patent No. 893 216 issued February 15, 1972 to M. Bunga and C.V. Thomas.
The film, after manufacture, is slit longitudinally into appropriate widths. The width is selected on the basis of the diameter of the tube to be formed on the vertical form, fill and seal apparatus.
The preferred method of manufacture of the multilayer film is by using a blown film coextrusion process, although other methods of manufacture of the film may be used.
It will be understood by those skilled in the art that additives e.g. UV stabilizers, anti-block agents, slip additives, may be added to the polymers from which the pouches of the present invention are made.
The pouches of the present invention may be used in the packaging of f lowable materials a . g . liquids , as def fined above .
In particular, the pouches may be used in the packaging of milk.
The multilayer film of the invention is particularly useful in the formation of pouches, especially using a form, fill and seal apparatus. In particular, the multilayer film ~2 ~ 82524 provides increased stiffness, compared to the monolayer sealant film, increased clarity compared to HDPE film, and further improves efficiencies in the runnability of monolayer sealant films as described herein.
The multilayer film may be used in the formation of pouches, for the packaging of flowable materials. In particular, the multilayer film may be used in the packaging of milk using a form, fill and seal apparatus.
EXAMPLE
Introduction Films were made on a five-layer blown film coextrusion line. The line consists of five extruders (A through E) feeding on an eight inch diameter circular die. The two "skin layer" extruders A and E were 2.5" (=65 mm) single-screw extruders, while the three "core" extruders B, C and D were 2"
(=50 mm). The line includes an oscillating nip, corona treater, edge guide and a back-to-back winder with slit-in line, capable of surface-driven or centre-driven winding. The width of the tower nip and winder also allow for blow-up ratios up to about 4:1.
Film Extrusion Formulations for the skin and core layers were preblended. A control linear low density polyethylene (LLDPE)/low density polyethylene (LDPE) blend, two single-site catalyst polymer formulations, and two high density polyethylenes were chosen:
Control 85% Sclair 11L4B octene LLDPE, density - 0.920 g/cc, M.I. - 0.75 15% Nova LF0521A LDPE, density = 0.921 g/cc, M.I.
- 5.0 Single Site Catalyst Film (SSC) SSC #1 52.5% Exact 3028 butene copolymer mPE, 0.900 g/cc density, M.I. - 1.20 40% Exact 4011 butene copolymer mPE, 0.887 g/cc density, M.I. - 2.20 3.4% Duex 8876 slip/antiblock concentrate 0.1% MB35102 antiblock concentrate 4.0% SAX 7401 extrusion aid concentrate (mPE means metallocene polyethylene) SSC #2 92.5% Exact 3033, butene-hexene terpolymer mPE, 0.900 g/cc density, M.I. - 1.20 3.4% Duex 8876 slip/antiblock concentrate 0.1% MB35102 antiblock concentrate 4.0% SAX 7401 extrusion aid concentrate AhAENDED SHEET
IPEA/EP
HDPE #1 Sclair 16A, 0.945 g/cc density, M.I. - 0.28 HDPE #2 Sclair 19C, 0.957 g/cc density, M.I. - 1.00 Film Layer A Layer B Layer C Layer D Layer E
(aatermost 03 mil ) 03 mil (innezmost) 0.4 and L0 mil L0 mil Controlas x s~l,airss r. sdair ss x sir ss r. s~lairss x sir 11L4B
IlL~s h x Nova 11L4B lIL4B 11LAB 1~ '. Nova LF0.521A 15 r. Nova is r. Nova IS : Novas LF052IA
Film SSC #1 8s r. Sdair 8s r. Sdair8s x Sdair SSC #1 I
(Exact 3028-ExactlIL4B lIL4B IIL4B (Exact 3028-Exact 40'11 blend)is x Nova is r. Nova is Y. Nova 4011 blend) FzZm SSC #1 Sdair 19C Sdair 19C Sdair 19C SSC #1 (Exact 3028-ExactHDPE HDPE HDPE (F~cact 3028-Exact 4011 blend) 4011 blend) Fdm SSC #2 8s x Sdair Sdair I6A 85 x Sdair SSC #2 (Exact 3033)I1L4B HDPE lIL4B (F~cact 3033) Is x Nova Is x Nova Film SSC #2 85 x Sclair Sclair 19C 85 T. SdairSSC #2 (Exact 3033)11L~B HDPE IIL.4B (Exact 3033) Is x No~a Is x Nova LFOSnA LFOSnA
All of the above identifiers are either trade-marks or designations available in the trade.
The control film was made at a blow up ratio of 2:1. The other films were made at a blow up ratio of 3:1. The films were would as a flattened tube and slit to a narrower width.
Film Testincr The films were run on the Prepac IS-6 filler to assess runnability, to make pouches for evaluating in a pitcher, and to make pouches for a pouch drop test.
A(~IENDED SHEET
IPEA/EP
WO 95121743 ~ ~ ~~ PCT/CA95/00064 Film Runnability of IS-6 Pouch-in-pitcher filler Control - good slip - stands up after - good pouch length opening - doesn't fold over edge of pitcher when pouring Film 1 - good slip - stiffness improved - some drag on forming relative the SCC
plates film referred to below Film 2 - p o a c h 1 a n g t -good stiffness h variation, i.e . long-short Film 3 -very good slip - very similar to properties control Film 4 -very good slip - very similar to properties control Previous - p o a c h 1 a n g - pouch tends to t h a 11 - S S variation, i . pouches fold over edge of C a .
f i 1 m s , get shorter and shorter p i t c h a r w h a n such as pouring, and stays E x a c t there 3 0 3 3 , D o w Af f inity For the pouch drop test, films were made into 1.3 litre water-filled pouches. For each pouch drop test, approximately 200 pouches were dropped on end from eleven feet onto a concrete floor. Results of the pouch drop impact test are shown in Figure 1.
Analysis From the results one can conclude that combining a core of HDPE with skin layers of a single-site or metallocene-catalyst polymers makes a film with improved clarity; adequate stiffness to run well on the existing IS-6; and good pouch drop impact resistance.
A structure such as these with mPE on the skin layers and other polymers in the core would have the advantage of the mPE's lower temperature sealing on the vertical seal.
The M11 test is described below.
The present invention further provides a multilayer polyethylene film formed from a layer of a sealant film and a stiffening layer of polyethylene; said sealant film being made from a composition comprising 10 to 100 parts by weight of a copolymer of ethylene and at least one Cq-Clo alpha-olefin manufactured in a polymerization process using a single-site polymerization catalyst and from 0 to 90 parts by weight of at least one polymer selected from the group consisting of a linear copolymer of ethylene and at least one C4-Clo alpha-olefin having a density of from 0.900 to 0.930 g/cm3 and a melt index of from 0.3 to 2.0 dg/min, a high-pressure polyethylene having a density of from 0.916 to 0.930 g/cm' and a melt index of from about 1 to 10 dg/min, and blends thereof;
said stiffening layer of polyethylene being of a thickness in the range of 5 to 110 microns and being formed from polyethylene having a density of at least 0.93 g/cm3 and a melt index of less than 5 dg/min; said multilayer film having a thickness of from 40 to 130 microns.
The present invention additionally provides a film formed from two layers of a sealant film and an interposed stiffening layer of a film having a higher stiffness than the sealant layer, said layer of higher stiffness being formed from a polymer having a melting point of not more than 140°C; said sealant film being made from a composition comprising 10 to 100 parts by weight of a copolymer of ethylene and at least one C4-Clo alpha-olefin manufactured in a polymerization process using a single-site polymerization catalyst and from 0 to 90 parts by weight of at least one polymer selected from the group consisting of a linear copolymer of ethylene and at least one C4-Clo alpha-olefin having a density of from 0.900 to 0.930 g/cm' and a melt index of from 0.3 to 2.0 dg/min, a high-pressure polyethylene having a density of from 0.916 to 0.930 g/cm3 and a melt index of from about 1 to 10 dg/min, and blends thereof; said interposed stiffening layer of higher stiffness being of a thickness in the range of 5 to 110 microns and being formed from polyethylene having a density of at least 0.93 g/cm3 and a melt index of less than 5 dg/min;
said laminate having a thickness of from 40 to 130 microns.
pN~Ef~IDcD SHEET
lPEAIFP
2 G ~25Z4 _ 7 _ The present invention also provides a multilayer film formed from a layer of a sealant film and a layer of a film having a higher stiffness than the sealant layer, said layer of higher stiffness being formed from a polymer having a melting point of not more than 140°C; said sealant film being made from a composition comprising 10 to 100 parts by weight of a copolymer of ethylene and at least one C4-Clo alpha-olefin manufactured in a polymerization process using a single-site polymerization catalyst and from 0 to 90 parts by weight of at least one polymer selected from the group consisting of a linear copolymer of ethylene and at least one C4-Clo alpha-olefin having a density of from 0.900 to 0.930 g/cm3 and a melt index of from 0.3 to 2.0 dg/min, a high-pressure polyethylene having a density of from 0.916 to 0.930 g/cm' and a melt index of from about 1 to 10 dg/min, and blends thereof;
said layer of higher stiffness being of a thickness in the range of 5 to 110 microns; said multilayer film having a thickness of from 40 to 130 microns.
In preferred embodiments of the multilayer film of the present invention, the film has a stiffness of at least 20 000 psi (=135 Mpa) , and especially at least 25 000 psi (=170 Mpa) .
The present invention also provides a pouch containing a flowable material, said pouch being made from a multilayer film in tubular form and having transversely heat sealed ends, said multilayer polyethylene film being formed from two layers of a sealant film and an interposed stiffening layer of polyethylene; said sealant film being made from a composition comprising 10 to 100 parts by weight of a copolymer of ethylene and at least one C4-Clo alpha-olefin manufactured in a polymerization process using a single-site polymerization catalyst and from 0 to 90 parts by weight of at least one polymer selected from the group consisting of a linear copolymer of ethylene and at least one C4-Clo alpha-olefin having a density of from 0.900 to 0.930 g/cm3 and a melt index of from 0.3 to 2.0 dg/min, a high-pressure polyethylene having a density of from 0.916 to 0.930 g/cm' and a melt index of f rom about 1 to 10 dg/min, and blends thereof ; said interposed stiffening layer of polyethylene being of a thickness in the range of 5 to 110 microns and being formed from polyethylene having a density of at least 0.93 g/cm' and a melt index of Ai~ENaED SHEET
IPEA/EP
_$-less than 5 dg/min; said multilayer film having a thickness of from 40 to 130 microns.
The present invention also provides a pouch for containing a flowable material, said pouch being made from a multilayer film in tubular form and having transversely heat sealed ends, said multilayer polyethylene film being formed from two layers of a sealant film and an interposed stiffening layer of polyethylene; said sealant film being made from a composition comprising 10 to 100 parts by weight of a copolymer of ethylene and at least one C4-Clo alpha-olefin manufactured in a polymerization process using a single-site polymerization catalyst and from 0 to 90 parts by weight of at least one polymer selected from the group consisting of a linear copolymer of ethylene and at least one C4-Clo alpha-olefin having a density of from 0.900 to 0.930 g/cm3 and a melt index of from 0.3 to 10.0 dg/min, a high-pressure polyethylene having a density of from 0.916 to 0.930 g/cm3 and a melt index of from about 1 to 10 dg/min, and blends thereof, said sealant film being selected on the basis of providing pouches with an M11-test value that is lower, at the same film thickness, than that for pouches made with a film of a blend of 85 parts of a linear ethylene/octene-1 copolymer having a density of about 0.920 g/cm3 and a melt index of about 0.75 dg/min and 15 parts of a high-pressure polyethylene having a density of about 0.918 g/cm3 and a melt index of 8.5 dg/min;
said interposed stiffening layer of polyethylene being of a thickness in the range of 5 to 110 microns and being from from polyethylene having a density of at least 0.93 g/cm3 and a melt index of less than 5 dg/min; said multilayer film having a thickness of from 40 to 130 microns.
In a preferred embodiment of the laminate and pouches of the present invention, the copolymer made with a single-site catalyst has a density in the range of 0.8-0.93 g/cm3 especially in the range of 0.88 to 0.91 g/cm3; and a melt index of less than 5 dg/min particularly in the range of 0.3 to 2 dg/min, and especially in the range of 0.5 to 1.5 dg/min.
In a further embodiment, the copolymer made with a single-site catalyst is an ethylene/butene-1 copolymer, an ethylene/hexene-1 copolymer, ethylene/octene-1 copolymer, ethylene/hexene-1/butene-1 terpolymer or an ethylene/octene 1/butene-1 terpolymer.
Adv~~~t~~~ ~~iEt'~
~PEA/Et~
2162~a24 _ g _ The present invention further provides a process for making pouches filled with a flowable material, using a vertical form, fill and seal apparatus, in which process each pouch is made from a flat web of film by forming a tubular film therefrom with a longitudinal seal and subsequently flattening the tubular film at a first position and transversely heat sealing said tubular film at the flattened position, filling the tubular film with a predetermined quantity of flowable material above said first position, flattening the tubular film above the predetermined quantity of flowable material at a second position and transversely heat sealing said tubular film at the second position, the improvement comprising making the pouches from a flat web of a film made from a multilayer film formed from two layers of a sealant film and an interposed stiffening layer of polyethylene; said sealant film being made from a composition comprising 10 to 100 parts by weight of a copolymer of ethylene and at least one C4-Clo alpha-olefin manufactured in a polymerization process using a single-site polymerization catalyst and from 0 to 90 parts by weight of at least one polymer selected from the group consisting of a linear copolymer of ethylene and at least one C4-Clo alpha-olefin having a density of from 0.900 to 0.930 g/cm' and a melt index of from 0.3 to 2.0 dg/min, a high-pressure polyethylene having a density of from 0.916 to 0.930 g/cm' and a melt index of from about 1 to 10 dg/min, and blends thereof ; said interposed stiffening layer of polyethylene being of a thickness in the range of 5 to 110 microns and being formed from polyethylene having a density of at least 0.93 g/cm3 and a melt index of less than 5 dg/min; said multilayer film having a thickness of from 50 to 100 microns.
The present invention also provides, in a process for making pouches filled with a flowable material, using a vertical form, fill and seal apparatus, in which process each pouch is made from a flat web of film by forming a tubular film therefrom with a longitudinal seal and subsequently flattening the tubular film at a first position and transversely heat sealing said tubular film at the flattened position, filling the tubular film with a predetermined quantity of flowable material above said first position, flattening the tubular film above the predetermined quantity AMENDED SHEET
tPEA/EP
2 l 8~~ 2 -la-of flowable material at a second position and transversely heat sealing said tubular film at the second position, the improvement comprising making the pouches from a flat web of film made from a composite formed from two layers of a sealant film and an interposed stiffening layer of polyethylene; said sealant film being made from a composition comprising 10 to 100 parts by weight of a copolymer of ethylene and at least one C4-Clo alpha-olefin manufactured in a polymerization process using a single-site polymerization catalyst and from 0 to 90 parts by weight of at least one polymer selected from the group consisting of a linear copolymer of ethylene and at least one C4-Clo alpha-olefin having a density of from 0.900 to 0.930 g/cm3 and a melt index of from 0.3 to 10.0 dg/min, a high-pressure polyethylene having a density of from 0.916 to 0.930 g/cm3 and a melt index of from about 1 to 10 dg/min, and blends thereof, said sealant film being selected on the basis of providing pouches with an Mll-test value that is lower, at the same film thickness, than that for pouches made with a film of a blend of 85 parts of a linear ethylene/octene-1 copolymer having a density of about 0.920 g/cm' and a melt index of about 0.75 dg/min and 15 parts of a high-pressure polyethylene having a density of about 0.918 g/cm' and a melt index of 8.5 dg/min.
Although melt index ranges are specified herein, it is understood that the polymers have melt indices typical of film-grade polymers.
Although the invention may be a multilayer film of a sealant film and another layer, especially polyethylene, and the related pouches and process described herein, the invention will be particularly described with reference to a multilayer or composite of two layers of sealant film and an interposed stiffening layer of polyethylene film. The latter multilayer films are preferred because of the ability to form a lap seal as well as a fin seal and the substantial absence of curl in the laminate. In addition, although the non-sealant layer may be a lyer of higher stiffness formed from a polymer having a melting point of not more than 140°C, that layer will be particularly described herein with reference to a layer of polyethylene.
The multilayer film is made, in part, from a composition comprising 10 to 100 parts by weight of a copolymer of a ,AMENDED SHEET
IPEA/EP
2 ~ 8 2524 copolymer of ethylene and at least one Cq-Clo alpha-olefin manufactured in a polymerization process using a single-site polymerization catalyst and from 0 to 90 parts by weight of at least one polymer selected from the group consisting of a linear copolymer of ethylene and at least one CQ-Clo alpha-olefin having a density of from 0.900 to 0.930 g/cm' and a melt index of from 0.3 to 2.0 dg/min, a high-pressure polyethylene having a density of from 0.916 to 0.924 g/cm3 and a melt index of from about 1 to 10 dg/min, and blends thereof .
In embodiments, the composition comprises 20-100 and especially 50-100 parts of the copolymer obtained using the single site catalyst, and conversely 0-80 and 0-50 parts of the other polymer specified above.
The polyethylene of the interlayer may be a so-called high-pressure polyethylene or a so-called linear polyethylene, and blends thereof. In embodiments, the polyethylene is 0 100% by weight of a high density polyethylene, including high molecular weight high density polyethylene, preferabloy 20 100% by weight of such polyethylene and in particular 75-100%
by weight of such polyethylene. The remainder of the polyethylene, if any, i.e., 0-80% by weight and especially 0-250 by weight, is a linear polyethylene or a recycled polyethylene obtained from any of a variety of sources provided that the recycled polyethylene meets the appropriate governmental or other regulations for packaging of the material that is to be packaged. The composition used for the interlayer (stiffening) needs to meet the density and melt index values specified herein viz. be a polyethylene having a density of at least 0.93 g/cm3 and a melt index of less than 1 dg/min.
Processes for the manufacture of so-called high pressure polyethylene from ethylene monomer have been operated commercially for decades. A variety of such polymers are available. The high pressure polyethylene of the sealant layer has a density of 0.916 to 0.930 g/cm3, especially 0.918 to 0.925 g/cm3. In addition, the high pressure polyethylene has a melt index in the range of 1 to 10 dg/min. and especially in the range of 0.5 to 5 dg/min. For the interposed layer, the high pressure polyethylene would have a density and melt index in the range described herein.
,~Nl~~;~~~ ~~iEE~
I~EA/E~' 2(8~5Z~
Processes for the commercial manufacture of linear polyethylene have been known for more than thirty years . Such processes may be operated at temperature above the solubilization temperature of the polymer in which event the polymer remains in solution, or the processes may be operated below the solubilization temperature in which event the polymer remains as a slurry in the polymerization solvent.
Processes are also known in which the polymerization is conducted in the gas phase in the absence of solvent. Other processes operate at both high temperature and high pressure.
The catalysts used are frequently based on titanium and are referred to as coordination catalysts; such catalysts may also be described as multi-site catalysts or heterogeneous catalysts. The polymer obtained is linear in nature, as opposed to the branched nature of high pressure polyethylene.
Linear low density polyethylene AMENDED SHEET
IPEA/EP
t WO 95/21743 ~ 2,,~( PCT/CA95/00064 is obtained by the co-polymerization of ethylene with at least one C9-Clo alpha-olefin hydrocarbon comonomer, examples of which include butene-1, hexene-1 and octene-1. The linear low density polyethylene has a density in the range of 0.900 to 0.930 g/cm3, preferably 0.912 to 0.930 g/cm3 and especially in the range of 0.918 to 0.925 g/cm3. In addition the polymer has a melt index in the range of 0.3 to 10.0 dg/min, preferably 0.3 to 2.0 dg/min and especially in the range of 0.5 to 1.5 dg/min.
The high density polyethylene has a density of at least 0.930 g/cm', especially in the range of 0.935-0.965 g/cm3.
Similarly, the high density polyethylene has a melt index of less than 1 dg/min and especially in the range of 0.01 to 0.3 dg/min; polymer in the lower end of that range may be classified as high molecular weight polyethylenes. The high density polyethylene may be high pressure polyethylene or linear polyethylene.
The ethylene copolymer made with single-site catalyst may be obtained using a variety of polymerization processes of the type described above for the manufacture of linear low density polyethylene e.g. processes that operate in solution, in the gas phase and as a slurry process; references to the use of single site catalysts in polymerization processes is made in Modern Plastics, p.15, May 1993, Plastics Focus Vol. 25, No.
12, June 21, 1993 and in Exxon Chemical Exact Facts, Vol.l, No.
1, February 1993. Such polymers are obtained by the co-polymerization of ethylene with at least one C4-Clo alpha-olefin hydrocarbon comonomer, examples of which include butene-1, hexene-1 and octene-1. The catalyst used is a so-called single-site catalyst, certain of which may also be referred to as metallocene or constrained geometry catalysts.
By the term "single-site catalyst" is meant a metallocene or constrained geometry catalyst. Metallocene catalysts are organometallic co-ordination compounds obtained as a cyclopentadienyl (Cp) derivative of a transition metal or metal halide. The metal is bonded to the Cp ring by electrons moving in orbitals extending above and below the plane of the ring (pi bond). Metallocene catalysts systems are extremely sensitive 2 I ~2~2~
to the geometry of the catalytic site at the transition metal (the "single-site"). Examples of single-site catalysts include CpzTICl2, Cp2ZrClz, CpzHfClZ, (CS (CH3) z) aTiCl2, PHZMe (Ind) ZZrCl2, (Me4Cpsi (Me) 2N(t-Bu) ] TiCHz [o-PhN (Mez) ] , Cp2Fe B (C2F2,4_ The polyethylene obtained with the single site catalyst preferably has a density in the range of 0.8 to 0.93 g/cm3, moreover in the range of 0.88 to 0.930 g/cm', and specially in the range of 0.89 to 0.910 g/cm'. In addition the polymer preferably has a melt index of less than 5 dg/min, particularly in the range of 0.3 to 2.0 dg/min and especially in the range of 0.5 to 1.5 dg/min. Preferred polymers include ethylene/butene-1, ethylene/hexene-1, ethylene/octene-1 and ethylene/hexene-1/butene-1 terpolymers.
The multilayer polyethylene film in one embodiment has a thickness of 40 to 130 microns, and especially in the range of 50 to 100 microns. In particular embodiments e.g. for use on a form, fill and seal apparatus, the laminate thickness is preferably in the range of 50 to 70 microns. The sealant layers on opposed sides of the interposed polyethylene layer are preferably of substantially equal thickness, although this is not essential provided that the requirements for the intended end-use are met, to allow the film to be reversed and/or opposing sides to be bonded together as in a tube. The interposed layer has a thickness of 5 to 110 microns, in one embodiment 5 to 50 microns and especially 8 to 16 microns in other embodiments.
The M11-test is as follows: In general terms, the M11-test is a drop test carried out on 1.3 litre water-filled pouches.
In the test, pouches containing 1.3 litres of water, at a temperature of 10~5'C, are made from a 32 cm. wide film web, on a Prepac IS-6 vertical form, fill and seal apparatus. The web of film is formed into a continuous tube with a lap seal, said tube having an inside diameter of approximately 9.8 cm. A
typical vertical sealing jaw of the Prepac IS-6 apparatus has an approximately 3.5 by 0.3 mm rectangular sealing wire made of Nichrome° alloy, and a transverse sealing jaw with an approximately 1.8 by 0.7 mm sealing wire made of Nichrome°
AMENDED Si~EET
IPEA/EP
WO 95/21743 ~ ~,a' PCT/CA95/00064 alloy. The operation of the vertical and transverse sealing element should be optimized for the particular film type and thickness used. Typically, during vertical sealing of the tube, a 35-50 amp current at 14-24 volts is passed through the sealing wire for about 0.2-0.5 seconds. The force applied by the vertical sealing jaws to the film is about 8 N applied for a dwell time of about 0.9 seconds. The vertical sealing jaw is cooled by water at 13'~6'C. During transverse sealing of the tube, a 35-55 amp current at 10-15 volts is passed through the sealing wire for about 0.2-0.5 seconds. The force applied by the transverse sealing jaws to the film is about 19 N applied for a dwell time of about 0.9 seconds. The transverse sealing jaw is cooled by water at 13'~6'C. Both sealing jaws are covered with 150 ~,m thick glass f fiber tape impregnated with Teflon° polytetrafluoroethylene resin. With respect to optimizing the sealing operations, it will be recognized that the sealing conditions (e. g. amperage, voltage, dwell time) depend on the gauge and melting characteristics of the film.
For example, a 50~Cm film would require lower amperage and voltage, as controlled by the rheostat on the apparatus, than would a 75~m film. Typically such a change in film thickness requires an adjustment of approximately 10% of the rheostat range.
The water-filled pouches containing the cold water, are dropped onto a concrete floor from a height of 335 cm. The pouches are positioned with the longitudinal axis of the tube i.e. pouch, coincident with an imaginary vertical line.
Any pouch from which water flows or weeps after the pouch has been dropped onto the floor, is termed a "leaker". The number of leakers, expressed as a percentage of the total number of pouches dropped is the M11-test value for the particular film being tested. It will be noted that the M11-test value will be affected by the thickness of the film as well as the material from which the film is made.
As noted above, it is the sealant film that is selected upon the basis of a drop test such as the M11-test. It is to be WO 95/21743 '~~ ~~ PCT/CA95/00064 understood, therefore, that pouches made with other pouch-forming apparatus come within the scope of the present invention.
The blends useful in the present invention may be made by blending the constituents prior to feeding to the hopper of a film extruder, or may be made by blending the constituents at the time of extrusion just prior to remelting in the extruder, or alternatively the constituents may be melt blended in the extruder.
The ethylene/a-olefin copolymer or blend of ethylene/a-olefin copolymer e.g. in pellet form, may be fed into a film extruder and extruded into film form using known techniques.
One preferred method of manufacturing film is the so-called blown film process disclosed in Canadian Patent No. 460 963 issued November S, 1949 to E.D. Fuller. Another preferred method of manufacturing film uses an internal or external cooling mandrel in the blown film process, as disclosed for example in Canadian Patent No. 893 216 issued February 15, 1972 to M. Bunga and C.V. Thomas.
The film, after manufacture, is slit longitudinally into appropriate widths. The width is selected on the basis of the diameter of the tube to be formed on the vertical form, fill and seal apparatus.
The preferred method of manufacture of the multilayer film is by using a blown film coextrusion process, although other methods of manufacture of the film may be used.
It will be understood by those skilled in the art that additives e.g. UV stabilizers, anti-block agents, slip additives, may be added to the polymers from which the pouches of the present invention are made.
The pouches of the present invention may be used in the packaging of f lowable materials a . g . liquids , as def fined above .
In particular, the pouches may be used in the packaging of milk.
The multilayer film of the invention is particularly useful in the formation of pouches, especially using a form, fill and seal apparatus. In particular, the multilayer film ~2 ~ 82524 provides increased stiffness, compared to the monolayer sealant film, increased clarity compared to HDPE film, and further improves efficiencies in the runnability of monolayer sealant films as described herein.
The multilayer film may be used in the formation of pouches, for the packaging of flowable materials. In particular, the multilayer film may be used in the packaging of milk using a form, fill and seal apparatus.
EXAMPLE
Introduction Films were made on a five-layer blown film coextrusion line. The line consists of five extruders (A through E) feeding on an eight inch diameter circular die. The two "skin layer" extruders A and E were 2.5" (=65 mm) single-screw extruders, while the three "core" extruders B, C and D were 2"
(=50 mm). The line includes an oscillating nip, corona treater, edge guide and a back-to-back winder with slit-in line, capable of surface-driven or centre-driven winding. The width of the tower nip and winder also allow for blow-up ratios up to about 4:1.
Film Extrusion Formulations for the skin and core layers were preblended. A control linear low density polyethylene (LLDPE)/low density polyethylene (LDPE) blend, two single-site catalyst polymer formulations, and two high density polyethylenes were chosen:
Control 85% Sclair 11L4B octene LLDPE, density - 0.920 g/cc, M.I. - 0.75 15% Nova LF0521A LDPE, density = 0.921 g/cc, M.I.
- 5.0 Single Site Catalyst Film (SSC) SSC #1 52.5% Exact 3028 butene copolymer mPE, 0.900 g/cc density, M.I. - 1.20 40% Exact 4011 butene copolymer mPE, 0.887 g/cc density, M.I. - 2.20 3.4% Duex 8876 slip/antiblock concentrate 0.1% MB35102 antiblock concentrate 4.0% SAX 7401 extrusion aid concentrate (mPE means metallocene polyethylene) SSC #2 92.5% Exact 3033, butene-hexene terpolymer mPE, 0.900 g/cc density, M.I. - 1.20 3.4% Duex 8876 slip/antiblock concentrate 0.1% MB35102 antiblock concentrate 4.0% SAX 7401 extrusion aid concentrate AhAENDED SHEET
IPEA/EP
HDPE #1 Sclair 16A, 0.945 g/cc density, M.I. - 0.28 HDPE #2 Sclair 19C, 0.957 g/cc density, M.I. - 1.00 Film Layer A Layer B Layer C Layer D Layer E
(aatermost 03 mil ) 03 mil (innezmost) 0.4 and L0 mil L0 mil Controlas x s~l,airss r. sdair ss x sir ss r. s~lairss x sir 11L4B
IlL~s h x Nova 11L4B lIL4B 11LAB 1~ '. Nova LF0.521A 15 r. Nova is r. Nova IS : Novas LF052IA
Film SSC #1 8s r. Sdair 8s r. Sdair8s x Sdair SSC #1 I
(Exact 3028-ExactlIL4B lIL4B IIL4B (Exact 3028-Exact 40'11 blend)is x Nova is r. Nova is Y. Nova 4011 blend) FzZm SSC #1 Sdair 19C Sdair 19C Sdair 19C SSC #1 (Exact 3028-ExactHDPE HDPE HDPE (F~cact 3028-Exact 4011 blend) 4011 blend) Fdm SSC #2 8s x Sdair Sdair I6A 85 x Sdair SSC #2 (Exact 3033)I1L4B HDPE lIL4B (F~cact 3033) Is x Nova Is x Nova Film SSC #2 85 x Sclair Sclair 19C 85 T. SdairSSC #2 (Exact 3033)11L~B HDPE IIL.4B (Exact 3033) Is x No~a Is x Nova LFOSnA LFOSnA
All of the above identifiers are either trade-marks or designations available in the trade.
The control film was made at a blow up ratio of 2:1. The other films were made at a blow up ratio of 3:1. The films were would as a flattened tube and slit to a narrower width.
Film Testincr The films were run on the Prepac IS-6 filler to assess runnability, to make pouches for evaluating in a pitcher, and to make pouches for a pouch drop test.
A(~IENDED SHEET
IPEA/EP
WO 95121743 ~ ~ ~~ PCT/CA95/00064 Film Runnability of IS-6 Pouch-in-pitcher filler Control - good slip - stands up after - good pouch length opening - doesn't fold over edge of pitcher when pouring Film 1 - good slip - stiffness improved - some drag on forming relative the SCC
plates film referred to below Film 2 - p o a c h 1 a n g t -good stiffness h variation, i.e . long-short Film 3 -very good slip - very similar to properties control Film 4 -very good slip - very similar to properties control Previous - p o a c h 1 a n g - pouch tends to t h a 11 - S S variation, i . pouches fold over edge of C a .
f i 1 m s , get shorter and shorter p i t c h a r w h a n such as pouring, and stays E x a c t there 3 0 3 3 , D o w Af f inity For the pouch drop test, films were made into 1.3 litre water-filled pouches. For each pouch drop test, approximately 200 pouches were dropped on end from eleven feet onto a concrete floor. Results of the pouch drop impact test are shown in Figure 1.
Analysis From the results one can conclude that combining a core of HDPE with skin layers of a single-site or metallocene-catalyst polymers makes a film with improved clarity; adequate stiffness to run well on the existing IS-6; and good pouch drop impact resistance.
A structure such as these with mPE on the skin layers and other polymers in the core would have the advantage of the mPE's lower temperature sealing on the vertical seal.
Claims (19)
1. A pouch formed from a mufti-layer film, which film has a stiffness of at least 20,000 psi (138 MPa) and wherein said film comprises at least one single-site catalyst sealant polymer layer and at least one stiffening layer of high density polyethylene being of greater stiffness than the single-site catalyst polymer layer.
2. The pouch as claimed in claim 1 wherein the stiffening layer of the film is a high pressure polyethylene or linear polyethylene or a blend thereof.
3. The pouch as claimed in claim 1 wherein the stiffening layer of the film is a polyethylene having a density of at least 0.930 g/cm3 and a melt index of less than 1 dg/min.
4. The pouch as claimed in claim 3 wherein the stiffening layer has a density in the range of 0.935 to 0.965 g/cm3 and a melt index in the range of 0.01 to 0.3 dg/min.
5. The pouch as claimed in any one of claims 1, 2, 3 or 4 wherein the stiffening layer of the film has a thickness in the range of 5 to 100 µm, and said film has a thickness of 40 to 130 µm.
6. The pouch as claimed in claim 5 wherein the stiffening layer has a thickness in the range of 5 to 50 µm, and said film has a thickness of 50 to 100 µm.
7. The pouch as claimed in claim 6 wherein the stiffening layer has a thickness in the range of 8 to 16 µm, and said film has a thickness of 50 to 70 µm.
8. The pouch as claimed in any one of claims 1, 2, 3 or 4 wherein the thickness of said stiffening layer of polyethylene is approximately 25 µm and that of the sealant layer is approximately 25 µm.
9. The pouch as claimed in any one of claims 1, 2, 3, 4, 5, 6, 7 or 8 wherein said stiffening layer of polyethylene is interposed between layers of single-site catalyst polymer.
10. The pouch as claimed in any one of claims 1, 2, 3, 4, 5, 6, 7, 8 or 9 wherein the film has a stiffness of at least 25,000 psi (175 MPa).
11. The pouch as claimed in any one of claims 1, 2, 3, 4, 5, 6, 7, 8, 9 or 10 wherein the sealant polymer layer comprises a copolymer of ethylene and at least one C4-C10 alpha-olefin manufactured in a single-site catalyst polymerization process.
12. The pouch as claimed in claim 11 wherein the sealant polymer layer further comprises at least one polymer selected from a linear copolymer of ethylene and at least one C4-C10 alpha-olefin other than a single-site catalysed polymer, a high pressure polyethylene and blends thereof.
13. The pouch as claimed in claim 12 wherein the sealant polymer layer comprises 10 to 100 parts by weight of said copolymer of ethylene and at least one C4-C10 alpha-olefin manufactured in a single-site catalyst polymerization process and from 0-90 parts by weight of at least one polymer selected from a linear copolymer of ethylene and at least one C4-C10 alpha-olefin other than a single-site catalysed polymer, a high pressure polyethylene and blends thereof.
14. The pouch of any one of claims 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12 or 13 in which the copolymer made with a single-site catalyst has a density in the range of 0.8-0.93 g/cm3, and a melt index of less than 5 dg/min.
15. The pouch of claim 14 in which the copolymer made with a single-site catalyst has a density in the range of 0.88-0.93 g/cm3, and a melt index in the range of 0.3 to 2.0 dg/min.
16. The pouch of claim 15 in which the copolymer made with a single-site catalyst has a density in the range of 0.89-0.910 g/cm3, and a melt index in the range of 0.5 to 1.5 dg/min.
17. The pouch in any one of claims 11, 12, 13, 14, 15 or 16 in which the copolymer made with a single-site catalyst is selected from ethylene/butene-1 copolymers, ethylene/hexene-1 copolymers, ethylene/octene-1 copolymers, ethylene-octene-1/butene-1 terpolymers and ethylene/hexene-1/butene-1 terpolymers.
18. A pouch according to claim 1 wherein the film comprises a multi-layer polyethylene film formed from two layers of a sealant film and an interposed stiffening layer of polyethylene; said sealant film being made from a composition comprising 10 to 100 parts by weight of a copolymer of ethylene and at least one C4-C10 alpha-olefin manufactured in a polymerization process using a single-site polymerization catalyst and from 0 to 90 parts by weight of at least one polymer selected from a linear copolymer of ethylene and at least one C4-C10 alpha-olefin having a density of from 0.900 to 0.930 g/cm3 and a melt index of from 0.3 to 10.0 dg/min other than a single-site catalysed polymer, a high-pressure polyethylene having a density of from 0.916 to 0.930 g/cm3 and a melt index of from about 1 to 10 dg/min, and blends thereof; said interposed stiffening layer of polyethylene being of a thickness in the range of 5 to 110 µm and being formed from polyethylene having a density of at least 0.93 g/cm3 and a melt index of less than 5 dg/min; said mufti-layer film having a thickness of from 40 to 130 µm.
19. A pouch according to claim 1 wherein the film comprised a layer of a sealant film and a stiffening layer of polyethylene; said sealant film being made from a composition comprising 10 to 100 parts by weight of a copolymer of ethylene and at least one C4-C10 alpha-olefin manufactured in a polymerization process using a single-site polymerization catalyst and from 0 to 90 parts by weight of at least one polymer selected from a linear copolymer of ethylene and at least one C4-C10 alpha-olefin having a density of from 0.900 to 0.930 g/cm3 and a melt index of from 0.3 to 10.0 dg/min other than a single-site catalysed polymer, a high-pressure polyethylene having a density of from 0.916 to 0.930 g/cm3 and a melt index of from about 1 to 10 dg/min, and blends thereof; said stiffening layer of polyethylene being of a thickness in the range of 5 to 110 µm and being formed from polyethylene having a density of at least 0.93 g/cm3 and a melt index of less than 5 dg/min; said mufti-layer film having a thickness of from 40 to 130 µm.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB9402430.4 | 1994-02-08 | ||
GB9402430A GB9402430D0 (en) | 1994-02-08 | 1994-02-08 | Multilayer ethylene copolymer film |
PCT/CA1995/000064 WO1995021743A1 (en) | 1994-02-08 | 1995-02-08 | Multilayer ethylene copolymer film |
Publications (2)
Publication Number | Publication Date |
---|---|
CA2182524A1 CA2182524A1 (en) | 1995-08-17 |
CA2182524C true CA2182524C (en) | 1999-12-14 |
Family
ID=10750075
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA002182524A Expired - Lifetime CA2182524C (en) | 1994-02-08 | 1995-02-08 | Multilayer ethylene copolymer film |
Country Status (7)
Country | Link |
---|---|
US (1) | US5972443A (en) |
EP (1) | EP0743902B2 (en) |
BR (1) | BR9506927A (en) |
CA (1) | CA2182524C (en) |
DE (1) | DE69505499T3 (en) |
GB (1) | GB9402430D0 (en) |
WO (1) | WO1995021743A1 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US10960649B2 (en) | 2017-11-14 | 2021-03-30 | Liqui-Box Corporation | Flex-crack resistant and thermally resistant aseptic bulk bags for flexible packaging |
Families Citing this family (44)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0701897B1 (en) * | 1994-09-16 | 2001-04-18 | Cryovac, Inc. | Thermoplastic multilayer film for use in packaging water |
IT1304704B1 (en) * | 1995-09-01 | 2001-03-28 | Manuli Stretch Spa | POLYETHYLENE MULTI-LAYER FILM |
US5879768A (en) * | 1995-10-06 | 1999-03-09 | The Dow Chemical Company | Pouches for packaging flowable materials |
WO1998006676A1 (en) | 1996-08-13 | 1998-02-19 | Nippon Sheet Glass Co., Ltd. | LASER MACHINING METHOD FOR GlASS SUBSTRATE, DIFFRACTION TYPE OPTICAL DEVICE FABRICATED BY THE MACHINING METHOD, AND METHOD OF MANUFACTURING OPTICAL DEVICE |
GB9620651D0 (en) * | 1996-10-02 | 1996-11-20 | Norester S A | A laminate |
US5843540A (en) * | 1996-11-15 | 1998-12-01 | Tetra Laval Holdings & Finance, S.A. | Multi-layer flexible container for flowable materials |
JP2001507296A (en) * | 1996-12-26 | 2001-06-05 | デュポン カナダ インコーポレイテッド | Film with improved sealing properties |
US6094889A (en) * | 1997-02-25 | 2000-08-01 | Exxon Chemical Patents, Inc. | Method of form and seal packaging |
IL131544A0 (en) | 1997-02-25 | 2001-01-28 | Exxon Chemical Patents Inc | Heat sealable films containing polyethylene and polypropylene |
EP0890611A1 (en) * | 1997-07-08 | 1999-01-13 | The Procter & Gamble Company | Packaging of flowable materials |
AU8605798A (en) * | 1997-08-04 | 1999-02-22 | Dow Chemical Company, The | Pouch for packaging flowable materials |
DE69828975T2 (en) | 1997-08-15 | 2006-01-12 | Dow Global Technologies, Inc., Midland | FILMS FROM ESSENTIALLY HOMOGENEOUS LINEAR OLEFINE POLYMERIC COMPOSITIONS |
US6416833B1 (en) | 1997-08-22 | 2002-07-09 | Dupont Canada Inc. | Interpolymer film pouch |
US6287700B1 (en) * | 1998-12-30 | 2001-09-11 | Exxon Mobil Oil Corporation | Multi-layer film with enhanced lamination bond strength |
US6383589B1 (en) * | 1999-03-29 | 2002-05-07 | Pechiney Plastic Packaging, Inc. | Multilayer plastic structures, containers made therefrom, and methods of making the structures |
EP1138702A1 (en) | 2000-03-30 | 2001-10-04 | Fina Research S.A. | Metallocene-produced polyethylene for glossy plastic containers |
US6440533B1 (en) | 2000-09-22 | 2002-08-27 | Tredegar Film Products Corporation | PVC replacement film |
US6592967B2 (en) | 2001-02-14 | 2003-07-15 | Avery Dennison Corporation | Microprism reflective sheeting with improved retention of reflectivity |
SE0100858D0 (en) * | 2001-03-12 | 2001-03-12 | Tetra Laval Holdings & Finance | Packaging laminate, method of producing a packaging container and the packaging container |
EP1300240A1 (en) * | 2001-10-02 | 2003-04-09 | Atofina Research S.A. | High ESCR glossy plastic containers |
KR101186268B1 (en) | 2002-06-26 | 2012-09-27 | 애버리 데니슨 코포레이션 | Oriented films comprising polypropylene/olefin elastomer blends |
MXPA05000289A (en) * | 2002-06-27 | 2005-09-20 | Pliant Corp | Lap sealable film with a peel layer. |
EP1750941A1 (en) * | 2004-05-07 | 2007-02-14 | A.W.A.X. PROGETTAZIONE E RICERCA S.r.l. | Extensible multilayer film |
JP4856371B2 (en) | 2004-11-10 | 2012-01-18 | 昭和電工パッケージング株式会社 | Laminated body for packaging, packaging bag body using the same, and packaging body for electronic material products |
ATE534699T1 (en) | 2006-04-26 | 2011-12-15 | Liqui Box Canada Inc | CRACKET-RESISTANT FILMS MADE OF LOW DENSITY POLYETHYLENE |
CN101466543B (en) | 2006-06-14 | 2014-03-19 | 艾利丹尼森公司 | Conformable and die-cuttable machine direction oriented labelstocks and labels, and process for preparing |
WO2007149900A2 (en) | 2006-06-20 | 2007-12-27 | Avery Dennison Corporation | Multilayered polymeric film for hot melt adhesive labeling and label stock and label thereof |
ES2379607T3 (en) | 2006-07-17 | 2012-04-27 | Avery Dennison Corporation | Asymmetric multilayer polymeric film and label thereof |
US8211533B2 (en) * | 2006-09-05 | 2012-07-03 | Liqui-Box Corporation | Resin blend of ethylene alpha olefin interpolymer and heterogeneous interpolymer for liquid packaging films |
CA2794597C (en) * | 2010-04-16 | 2021-05-04 | Liqui-Box Corporation | Multi-layer, ethylene polymer-based films with novel polypropylene blend-based stiffening layer |
BR112012025478A2 (en) | 2010-04-16 | 2019-09-24 | Liqui Box Corp | multilayer film to produce pouches to contain dispersible materials and process to produce pouches filled with a dispersible material |
WO2011130489A2 (en) * | 2010-04-16 | 2011-10-20 | Liqui-Box Corporation | Multi-layer, ethylene polymer-based films with high-density polyethylene based stiffening layer |
EP2397325A1 (en) | 2010-06-18 | 2011-12-21 | Cryovac, Inc. | Multilayer film for packaging fluid products |
US9676532B2 (en) | 2012-08-15 | 2017-06-13 | Avery Dennison Corporation | Packaging reclosure label for high alcohol content products |
KR102311420B1 (en) | 2013-12-31 | 2021-10-13 | 다우 글로벌 테크놀로지스 엘엘씨 | Multilayered films, methods of manufacture thereof and articles comprising the same |
WO2015123827A1 (en) | 2014-02-19 | 2015-08-27 | Dow Global Technologies Llc | High performance sealable co-extruded oriented film, methods of manufacture thereof and articles comprising the same |
US20150231862A1 (en) | 2014-02-19 | 2015-08-20 | Dow Global Technologies Llc | Multilayered polyolefin films, methods of manufacture thereof and articles comprising the same |
AU2015270854B2 (en) | 2014-06-02 | 2018-08-02 | Avery Dennison Corporation | Films with enhanced scuff resistance, clarity, and conformability |
WO2017096211A1 (en) * | 2015-12-02 | 2017-06-08 | Berry Plastics Corporation | Peelable film for container lid |
WO2018102091A1 (en) | 2016-12-02 | 2018-06-07 | Exxonmobil Chemical Patents Inc. | Polyethylene films |
ES1189859Y (en) | 2017-07-31 | 2017-11-06 | Liquibox Spain Sl | STERILIZING MACHINE FOR LIQUID CONTAINER BAGS |
US11383910B2 (en) | 2017-09-13 | 2022-07-12 | Liqui-Box Corporation | Process for preventing organoleptic degradation in flexibly-packaged sensitive foods and packaged products thereof |
EP3569411A1 (en) | 2018-05-18 | 2019-11-20 | Dow Global Technologies Llc | Spout pouch and method of making same |
US20230264449A1 (en) * | 2020-06-24 | 2023-08-24 | Trioworld Nyborg A/S | Tubular film for stretch hoods comprising recycled material |
Family Cites Families (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AU565262B2 (en) † | 1982-06-02 | 1987-09-10 | Du Pont Canada Inc. | Pouches of copolymer film |
MX9200724A (en) * | 1991-02-22 | 1993-05-01 | Exxon Chemical Patents Inc | HEAT SEALABLE MIX OF POLYETHYLENE OR PLASTOMER OF VERY LOW DENSITY WITH POLYMERS BASED ON POLYPROPYLENE AND THERMAL SEALABLE FILM AS WELL AS ARTICLES MADE WITH THOSE. |
AU660043B2 (en) * | 1991-07-18 | 1995-06-08 | Exxon Chemical Patents Inc. | Heat sealed article |
US5288531A (en) † | 1991-08-09 | 1994-02-22 | The Dow Chemical Company | Pouch for packaging flowable materials |
US5278272A (en) * | 1991-10-15 | 1994-01-11 | The Dow Chemical Company | Elastic substantialy linear olefin polymers |
US5562958A (en) † | 1991-10-15 | 1996-10-08 | The Dow Chemical Company | Packaging and wrapping film |
US5206075A (en) * | 1991-12-19 | 1993-04-27 | Exxon Chemical Patents Inc. | Sealable polyolefin films containing very low density ethylene copolymers |
JP3326873B2 (en) * | 1992-07-22 | 2002-09-24 | 住友化学工業株式会社 | Packaging film |
DE69308153T3 (en) * | 1992-09-16 | 2012-04-05 | Exxonmobil Chemical Patents, Inc. (N.D.Ges.D. Staates Delaware) | SOFT FILMS WITH IMPROVED PHYSICAL PROPERTIES |
ES2096949T3 (en) * | 1992-10-02 | 1997-03-16 | Du Pont | IMPROVED RETRACTILE FILM AND PROCEDURES RELATED TO IT. |
US5604043A (en) * | 1993-09-20 | 1997-02-18 | W.R. Grace & Co.-Conn. | Heat shrinkable films containing single site catalyzed copolymers having long chain branching |
-
1994
- 1994-02-08 GB GB9402430A patent/GB9402430D0/en active Pending
-
1995
- 1995-02-08 DE DE69505499T patent/DE69505499T3/en not_active Expired - Lifetime
- 1995-02-08 WO PCT/CA1995/000064 patent/WO1995021743A1/en active IP Right Grant
- 1995-02-08 US US08/693,189 patent/US5972443A/en not_active Expired - Lifetime
- 1995-02-08 CA CA002182524A patent/CA2182524C/en not_active Expired - Lifetime
- 1995-02-08 BR BRPI9506927-5A patent/BR9506927A/en not_active IP Right Cessation
- 1995-02-08 EP EP95907530A patent/EP0743902B2/en not_active Expired - Lifetime
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US10960649B2 (en) | 2017-11-14 | 2021-03-30 | Liqui-Box Corporation | Flex-crack resistant and thermally resistant aseptic bulk bags for flexible packaging |
Also Published As
Publication number | Publication date |
---|---|
WO1995021743A1 (en) | 1995-08-17 |
EP0743902A1 (en) | 1996-11-27 |
CA2182524A1 (en) | 1995-08-17 |
EP0743902B2 (en) | 2005-12-21 |
DE69505499T3 (en) | 2006-09-21 |
DE69505499D1 (en) | 1998-11-26 |
BR9506927A (en) | 1997-09-30 |
DE69505499T2 (en) | 1999-04-29 |
GB9402430D0 (en) | 1994-03-30 |
EP0743902B1 (en) | 1998-10-21 |
US5972443A (en) | 1999-10-26 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CA2182524C (en) | Multilayer ethylene copolymer film | |
AU704902B2 (en) | Novel pouches for packaging flowable materials | |
US6767599B2 (en) | Process for manufacturing pouches of ethylene copolymer film for containing a flowable material | |
CA2165340C (en) | Pouch for packaging flowable materials | |
US6117465A (en) | Pouches for packaging flowable materials | |
EP0865361B1 (en) | Novel pouches for packaging flowable materials in pouches | |
US8978346B2 (en) | Multi-layer, ethylene polymer-based films with high-density polyethylene based stiffening layer | |
US9757926B2 (en) | Multi-layer ethylene polymer-based films with polypropylene-based stiffening layer | |
EP0998388B1 (en) | Pouches for packaging flowable materials | |
WO1999052972A1 (en) | Peelable-seal polyolefin composition and sealant layer | |
EP0948432A1 (en) | Films having improved sealing properties | |
EP1112321A1 (en) | Liquid packages having improved leaker frequency performance | |
NZ336920A (en) | Pouches for packaging flowable materials with polymeric composition comprising 5-95% ethylene copolymer and C3-C18 alpha olefin |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
EEER | Examination request | ||
MKEX | Expiry |
Effective date: 20150209 |