WO2012093881A2 - Method for manufacturing a multi-layer oriented polyolefin film and multi-layer oriented polyolefin film manufactured thereby - Google Patents
Method for manufacturing a multi-layer oriented polyolefin film and multi-layer oriented polyolefin film manufactured thereby Download PDFInfo
- Publication number
- WO2012093881A2 WO2012093881A2 PCT/KR2012/000140 KR2012000140W WO2012093881A2 WO 2012093881 A2 WO2012093881 A2 WO 2012093881A2 KR 2012000140 W KR2012000140 W KR 2012000140W WO 2012093881 A2 WO2012093881 A2 WO 2012093881A2
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- layer
- film
- resin
- resin layer
- extrusion
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims abstract description 50
- 229920000098 polyolefin Polymers 0.000 title claims abstract description 37
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 24
- 229920005989 resin Polymers 0.000 claims abstract description 148
- 239000011347 resin Substances 0.000 claims abstract description 148
- 238000001125 extrusion Methods 0.000 claims abstract description 80
- 238000002844 melting Methods 0.000 claims abstract description 26
- 239000010410 layer Substances 0.000 claims description 277
- 238000001816 cooling Methods 0.000 claims description 53
- 239000000463 material Substances 0.000 claims description 34
- 239000002216 antistatic agent Substances 0.000 claims description 25
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 21
- 239000005038 ethylene vinyl acetate Substances 0.000 claims description 20
- 239000012792 core layer Substances 0.000 claims description 18
- DQXBYHZEEUGOBF-UHFFFAOYSA-N but-3-enoic acid;ethene Chemical compound C=C.OC(=O)CC=C DQXBYHZEEUGOBF-UHFFFAOYSA-N 0.000 claims description 16
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 claims description 15
- 229920005672 polyolefin resin Polymers 0.000 claims description 15
- 239000012748 slip agent Substances 0.000 claims description 13
- 239000004677 Nylon Substances 0.000 claims description 12
- 229920001778 nylon Polymers 0.000 claims description 12
- 239000002981 blocking agent Substances 0.000 claims description 10
- 230000008018 melting Effects 0.000 claims description 10
- 229920001897 terpolymer Polymers 0.000 claims description 8
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 7
- 239000005977 Ethylene Substances 0.000 claims description 7
- 239000002253 acid Substances 0.000 claims description 6
- 229920006122 polyamide resin Polymers 0.000 claims description 4
- XSMJZKTTXZAXHD-UHFFFAOYSA-N ethene;2-methylprop-2-enoic acid Chemical compound C=C.CC(=C)C(O)=O XSMJZKTTXZAXHD-UHFFFAOYSA-N 0.000 claims description 3
- VNPZMCWUXKJOHF-UHFFFAOYSA-N ethene;methyl acetate Chemical compound C=C.COC(C)=O VNPZMCWUXKJOHF-UHFFFAOYSA-N 0.000 claims description 3
- 239000004925 Acrylic resin Substances 0.000 claims description 2
- 229920000178 Acrylic resin Polymers 0.000 claims description 2
- QHIWVLPBUQWDMQ-UHFFFAOYSA-N butyl prop-2-enoate;methyl 2-methylprop-2-enoate;prop-2-enoic acid Chemical compound OC(=O)C=C.COC(=O)C(C)=C.CCCCOC(=O)C=C QHIWVLPBUQWDMQ-UHFFFAOYSA-N 0.000 claims description 2
- 229920001971 elastomer Polymers 0.000 claims description 2
- 229920002050 silicone resin Polymers 0.000 claims description 2
- 229920002803 thermoplastic polyurethane Polymers 0.000 claims description 2
- 238000003475 lamination Methods 0.000 abstract description 12
- 230000008569 process Effects 0.000 abstract description 11
- 239000004743 Polypropylene Substances 0.000 description 37
- 229920001155 polypropylene Polymers 0.000 description 37
- 239000004698 Polyethylene Substances 0.000 description 32
- 229920000573 polyethylene Polymers 0.000 description 28
- 238000000576 coating method Methods 0.000 description 14
- 239000011229 interlayer Substances 0.000 description 14
- 239000011127 biaxially oriented polypropylene Substances 0.000 description 11
- 239000011248 coating agent Substances 0.000 description 11
- -1 polypropylene Polymers 0.000 description 11
- 229920006378 biaxially oriented polypropylene Polymers 0.000 description 9
- 239000000654 additive Substances 0.000 description 8
- 230000000052 comparative effect Effects 0.000 description 8
- 239000005022 packaging material Substances 0.000 description 7
- 239000000047 product Substances 0.000 description 7
- 239000011342 resin composition Substances 0.000 description 6
- 238000004804 winding Methods 0.000 description 6
- 235000013305 food Nutrition 0.000 description 5
- 229920002292 Nylon 6 Polymers 0.000 description 4
- 239000004840 adhesive resin Substances 0.000 description 4
- 229920006223 adhesive resin Polymers 0.000 description 4
- 239000002131 composite material Substances 0.000 description 4
- 238000004806 packaging method and process Methods 0.000 description 4
- 238000007789 sealing Methods 0.000 description 4
- JHWNWJKBPDFINM-UHFFFAOYSA-N Laurolactam Chemical compound O=C1CCCCCCCCCCCN1 JHWNWJKBPDFINM-UHFFFAOYSA-N 0.000 description 3
- 229920000299 Nylon 12 Polymers 0.000 description 3
- 229920002302 Nylon 6,6 Polymers 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- 230000000996 additive effect Effects 0.000 description 3
- 239000000853 adhesive Substances 0.000 description 3
- 230000001070 adhesive effect Effects 0.000 description 3
- 229920001940 conductive polymer Polymers 0.000 description 3
- 238000010924 continuous production Methods 0.000 description 3
- 239000003792 electrolyte Substances 0.000 description 3
- 238000000926 separation method Methods 0.000 description 3
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
- 239000004594 Masterbatch (MB) Substances 0.000 description 2
- 230000015556 catabolic process Effects 0.000 description 2
- 239000013065 commercial product Substances 0.000 description 2
- 238000011109 contamination Methods 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 238000006731 degradation reaction Methods 0.000 description 2
- 230000001788 irregular Effects 0.000 description 2
- 238000010030 laminating Methods 0.000 description 2
- 229920000139 polyethylene terephthalate Polymers 0.000 description 2
- 239000005020 polyethylene terephthalate Substances 0.000 description 2
- 239000004800 polyvinyl chloride Substances 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- 238000009823 thermal lamination Methods 0.000 description 2
- 238000009966 trimming Methods 0.000 description 2
- PZWQOGNTADJZGH-SNAWJCMRSA-N (2e)-2-methylpenta-2,4-dienoic acid Chemical compound OC(=O)C(/C)=C/C=C PZWQOGNTADJZGH-SNAWJCMRSA-N 0.000 description 1
- HGUFODBRKLSHSI-UHFFFAOYSA-N 2,3,7,8-tetrachloro-dibenzo-p-dioxin Chemical compound O1C2=CC(Cl)=C(Cl)C=C2OC2=C1C=C(Cl)C(Cl)=C2 HGUFODBRKLSHSI-UHFFFAOYSA-N 0.000 description 1
- ZXVONLUNISGICL-UHFFFAOYSA-N 4,6-dinitro-o-cresol Chemical compound CC1=CC([N+]([O-])=O)=CC([N+]([O-])=O)=C1O ZXVONLUNISGICL-UHFFFAOYSA-N 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- 229920003312 Appeel® Polymers 0.000 description 1
- 229920002799 BoPET Polymers 0.000 description 1
- 239000005909 Kieselgur Substances 0.000 description 1
- 229910001290 LiPF6 Inorganic materials 0.000 description 1
- 229920001609 Poly(3,4-ethylenedioxythiophene) Polymers 0.000 description 1
- 229920000265 Polyparaphenylene Polymers 0.000 description 1
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 1
- HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 230000004888 barrier function Effects 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical class [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- HQQADJVZYDDRJT-UHFFFAOYSA-N ethene;prop-1-ene Chemical group C=C.CC=C HQQADJVZYDDRJT-UHFFFAOYSA-N 0.000 description 1
- 238000007765 extrusion coating Methods 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 235000013611 frozen food Nutrition 0.000 description 1
- 239000010954 inorganic particle Substances 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 239000002346 layers by function Substances 0.000 description 1
- 229940127554 medical product Drugs 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 231100000956 nontoxicity Toxicity 0.000 description 1
- 230000009965 odorless effect Effects 0.000 description 1
- FATBGEAMYMYZAF-KTKRTIGZSA-N oleamide Chemical compound CCCCCCCC\C=C/CCCCCCCC(N)=O FATBGEAMYMYZAF-KTKRTIGZSA-N 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 229920006280 packaging film Polymers 0.000 description 1
- 239000012785 packaging film Substances 0.000 description 1
- 229920000553 poly(phenylenevinylene) Polymers 0.000 description 1
- 229920001197 polyacetylene Polymers 0.000 description 1
- 229920000767 polyaniline Polymers 0.000 description 1
- 229920000069 polyphenylene sulfide Polymers 0.000 description 1
- 229920000128 polypyrrole Polymers 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 229920000123 polythiophene Polymers 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 238000004064 recycling Methods 0.000 description 1
- 229910000077 silane Inorganic materials 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 229920006027 ternary co-polymer Polymers 0.000 description 1
- 230000002087 whitening effect Effects 0.000 description 1
Images
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
- B32B25/00—Layered products comprising a layer of natural or synthetic rubber
- B32B25/04—Layered products comprising a layer of natural or synthetic rubber comprising rubber as the main or only constituent of a layer, which is next to another layer of the same or of a different material
- B32B25/08—Layered products comprising a layer of natural or synthetic rubber comprising rubber 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
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C55/00—Shaping by stretching, e.g. drawing through a die; Apparatus therefor
- B29C55/02—Shaping by stretching, e.g. drawing through a die; Apparatus therefor of plates or sheets
- B29C55/10—Shaping by stretching, e.g. drawing through a die; Apparatus therefor of plates or sheets multiaxial
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C48/00—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
- B29C48/001—Combinations of extrusion moulding with other shaping operations
- B29C48/0013—Extrusion moulding in several steps, i.e. components merging outside the die
- B29C48/0014—Extrusion moulding in several steps, i.e. components merging outside the die producing flat articles having components brought in contact outside the extrusion die
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C48/00—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
- B29C48/03—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor characterised by the shape of the extruded material at extrusion
- B29C48/07—Flat, e.g. panels
- B29C48/08—Flat, e.g. panels flexible, e.g. films
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C48/00—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
- B29C48/25—Component parts, details or accessories; Auxiliary operations
- B29C48/88—Thermal treatment of the stream of extruded material, e.g. cooling
- B29C48/911—Cooling
- B29C48/9135—Cooling of flat articles, e.g. using specially adapted supporting means
- B29C48/914—Cooling drums
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C48/00—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
- B29C48/25—Component parts, details or accessories; Auxiliary operations
- B29C48/88—Thermal treatment of the stream of extruded material, e.g. cooling
- B29C48/911—Cooling
- B29C48/9135—Cooling of flat articles, e.g. using specially adapted supporting means
- B29C48/9175—Cooling of flat articles, e.g. using specially adapted supporting means by interposing a fluid layer between the supporting means and the flat article
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C55/00—Shaping by stretching, e.g. drawing through a die; Apparatus therefor
- B29C55/02—Shaping by stretching, e.g. drawing through a die; Apparatus therefor of plates or sheets
- B29C55/04—Shaping by stretching, e.g. drawing through a die; Apparatus therefor of plates or sheets uniaxial, e.g. oblique
- B29C55/06—Shaping by stretching, e.g. drawing through a die; Apparatus therefor of plates or sheets uniaxial, e.g. oblique parallel with the direction of feed
-
- 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
- B32B25/00—Layered products comprising a layer of natural or synthetic rubber
- B32B25/20—Layered products comprising a layer of natural or synthetic rubber comprising silicone rubber
-
- 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
-
- 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
- B32B27/18—Layered products comprising a layer of synthetic resin characterised by the use of special additives
-
- 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
- B32B27/00—Layered products comprising a layer of synthetic resin
- B32B27/34—Layered products comprising a layer of synthetic resin comprising polyamides
-
- 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
- B32B27/40—Layered products comprising a layer of synthetic resin comprising polyurethanes
-
- 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
- B32B37/00—Methods or apparatus for laminating, e.g. by curing or by ultrasonic bonding
- B32B37/14—Methods or apparatus for laminating, e.g. by curing or by ultrasonic bonding characterised by the properties of the layers
- B32B37/15—Methods or apparatus for laminating, e.g. by curing or by ultrasonic bonding characterised by the properties of the layers with at least one layer being manufactured and immediately laminated before reaching its stable state, e.g. in which a layer is extruded and laminated while in semi-molten state
- B32B37/153—Methods or apparatus for laminating, e.g. by curing or by ultrasonic bonding characterised by the properties of the layers with at least one layer being manufactured and immediately laminated before reaching its stable state, e.g. in which a layer is extruded and laminated while in semi-molten state at least one layer is extruded and immediately laminated while in semi-molten state
-
- 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
- B32B38/00—Ancillary operations in connection with laminating processes
- B32B38/0012—Mechanical treatment, e.g. roughening, deforming, stretching
-
- 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
- B32B38/00—Ancillary operations in connection with laminating processes
- B32B38/06—Embossing
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J5/00—Manufacture of articles or shaped materials containing macromolecular substances
- C08J5/18—Manufacture of films or sheets
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C48/00—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
- B29C48/001—Combinations of extrusion moulding with other shaping operations
- B29C48/0018—Combinations of extrusion moulding with other shaping operations combined with shaping by orienting, stretching or shrinking, e.g. film blowing
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29K—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
- B29K2021/00—Use of unspecified rubbers as moulding material
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29K—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
- B29K2023/00—Use of polyalkenes or derivatives thereof as moulding material
- B29K2023/04—Polymers of ethylene
- B29K2023/06—PE, i.e. polyethylene
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29K—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
- B29K2023/00—Use of polyalkenes or derivatives thereof as moulding material
- B29K2023/04—Polymers of ethylene
- B29K2023/08—Copolymers of ethylene
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29K—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
- B29K2023/00—Use of polyalkenes or derivatives thereof as moulding material
- B29K2023/04—Polymers of ethylene
- B29K2023/08—Copolymers of ethylene
- B29K2023/083—EVA, i.e. ethylene vinyl acetate copolymer
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29K—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
- B29K2023/00—Use of polyalkenes or derivatives thereof as moulding material
- B29K2023/10—Polymers of propylene
- B29K2023/12—PP, i.e. polypropylene
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29K—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
- B29K2075/00—Use of PU, i.e. polyureas or polyurethanes or derivatives thereof, as moulding material
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29K—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
- B29K2077/00—Use of PA, i.e. polyamides, e.g. polyesteramides or derivatives thereof, as moulding material
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29K—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
- B29K2083/00—Use of polymers having silicon, with or without sulfur, nitrogen, oxygen, or carbon only, in the main chain, as moulding material
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29K—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
- B29K2105/00—Condition, form or state of moulded material or of the material to be shaped
- B29K2105/0005—Condition, form or state of moulded material or of the material to be shaped containing compounding ingredients
- B29K2105/0008—Anti-static agents
-
- 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
- B32B38/00—Ancillary operations in connection with laminating processes
- B32B38/0012—Mechanical treatment, e.g. roughening, deforming, stretching
- B32B2038/0028—Stretching, elongating
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2307/00—Properties of the layers or laminate
- B32B2307/70—Other properties
- B32B2307/746—Slipping, anti-blocking, low friction
-
- 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
-
- 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
- B32B37/00—Methods or apparatus for laminating, e.g. by curing or by ultrasonic bonding
- B32B37/08—Methods or apparatus for laminating, e.g. by curing or by ultrasonic bonding characterised by the cooling method
Definitions
- This disclosure relates to a method for manufacturing a multi-layer oriented polyolefin film, and a multi-layer oriented polyolefin film manufactured thereby.
- multi-layer oriented polyolefin films such as polypropylene (PP) or polyethylene (PE) films
- PP polypropylene
- PE polyethylene
- laminated sheets laminated sheets
- PVC polyvinyl chloride
- PET polyethylene terephthalate
- PVC films may emit harmful materials, such as dioxin, upon incineration, and PET films may not be cost-efficient and have a difficulty in recycling.
- multi-layer oriented polyolefin films advantageous in terms of cost-efficiency and recyclability, particularly multi-layer biaxially oriented polypropylene (BOPP) films have been used more frequently.
- BOPP films are advantageous in terms of cost-efficiency and recyclability, and also have an excellece in mechanical properties such as tensile strength, rigidity, surface hardness and impact resistance, optical properties such as gloss and transparency, and food hygiene characteristics such as non-toxicity and odorless characteristics.
- they are useful for packaging materials (food packaging, etc.) or lamination coating (laminated sheets).
- Fig. 1 is a schematic structural view of a conventional general BOPP film
- Fig. 2 is a schematic view illustrating a method for manufacturing a BOPP film according to the related art.
- a BOPP film generally includes a PP layer as a core layer 3, and a skin outer layer 1 and a skin inner layer 2 stacked on one side and the other side of the core layer 3, respectively.
- the skin outer layer 1 comprises PP
- the skin inner layer 2 comprises PP or PE.
- a functional resin layer 4 may be stacked on the skin outer layer 1 and/or skin inner layer 2.
- the functional layer 4 may include a low-melting point adhesive resin such as ethylene vinyl acetate (EVA) or polyethylene (PE) capable of hot-melting (heat sealing).
- EVA ethylene vinyl acetate
- PE polyethylene
- the skin outer layer 1, core layer 3 and the skin inner layer 2 are co-extruded through an extruder 5 so that the three layers 1, 2, 3 are laminated at extrusion dies. In this manner, it is possible to form a multi-layer film. Then, the extruded multi-layer film is passed through a cooling roll 6 so that it is cooled, and then is subjected to biaxial orientation, i.e., the machine direction orientation (MDO) and successive transverse direction orientation (TDO).
- MDO machine direction orientation
- TDO successive transverse direction orientation
- the extruded multi-layer film is passed through an machine direction orientation device 7 having multiple roll combinations R to carry out the orientation along the machine direction (i.e., longditudinal direction). Then, the machine direction oriented film is passed continuously to a transverse direction orientation device 8 to carry out the orientation along the transverse direction by way of a rail pattern. After that, the machine direction and transverse direction oriented film is wound at a winding roll 9.
- a method for manufacturing a multi-layer BOPP film according to the related art includes extrusion, cooling, MD orientation and TD orientation so as to provide a multi-layer film having a structure of PP layer/PP layer/PP (or PE) layer as shown, for example, in Fig. 1.
- a functional resin layer 4 is further laminated on the skin outer layer 1 and/or skin inner layer 2, as mentioned above. That is, in the method according to the related art, the functional resin layer 4 such as ethylene vinyl acetate (EVA), etc. is laminated through additional processes such as coating, lamination (hot-melting), etc. However, such additional processes are complicated and take much time and cost.
- EVA ethylene vinyl acetate
- a co-extrusion method including introducing the functional resin into the skin extrusion section upon the multi-layer extrusion coating may be contemplated.
- the functional resin and polyolefin e.g. PP
- such co-extrusion may be difficult. That is, low-melting point resins or resins other than polyolefin resins are not amenable to the co-extrusion.
- a low-melting point resin such as EVA
- its melting point difference from PP causes degradation of interlayer adhesion strength (adhesive force).
- the resin layer 4 may be scratched, resulting in degradation of an appearance of the resultant product. Further, the resin layer 4 may be stuck to the rolls R, thereby making it difficult to carry out the co-extrusion.
- the method for laminating a functional resin layer 4 according to the related art requires additional processes such as coating or lamination (hot-melting) which require a relatively long time and high cost, and as a result, cause an increase in manufacturing cost.
- This disclosure is directed to providing a method for manufacturing a multi-layer oriented polyolefin film, which allows even a low-melting point functional resin to be laminated through a continuous process and allows a simple and time-efficient process to reduce a manufacturing cost of products.
- This disclosure is also directed to providing a multi-layer oriented polyolefin film obtained by the method.
- a method for manufacturing a multi-layer oriented polyolefin film including: carrying out a first extrusion molding of a multi-layer polyolefin film; first cooling the first extrusion molded film; machine direction orienting the first cooled film along the longditudinal direction; carrying out a second extrusion molding in order to laminate at least one resin layer on the machine direction oriented film; second cooling the film laminated with the resin layer; and transverse direction orienting the second cooled film along the transverse direction.
- the second cooling of the film laminated with the resin layer may be carried out by using a cooling roll having an uneven structure on its surface to form air flow grooves on the resin layer.
- a multi-layer oriented polyolefin film obtained by the above-described method.
- a machine direction orientation is followed by an additional extrusion/cooling (i.e., second extrusion/second cooling), wherein a resin layer is laminated through the additional extrusion.
- second extrusion/second cooling i.e., second extrusion/second cooling
- a resin layer is laminated through the additional extrusion.
- a low-melting point resin may be laminated through the extrusion.
- multiple layers, including a resin layer may be laminated through such continuous extrusion to provide a multi-layer oriented polyolefin film. Accordingly, the method has a simple process, is time-efficient, and reduces the manufacture cost of products.
- Fig. 1 is a schematic structural view of a general conventional biaxially oriented polypropylene (BOPP) film.
- BOPP biaxially oriented polypropylene
- Fig. 2 is a schematic view of manufacturing apparatus illustrating a conventional method for manufacturing a BOPP film according to the related art
- Figs. 3 and 4 are schematic structural views illustrating the multi-layer oriented polyolefin films according to embodiments.
- Fig. 5 is a schematic view of manufacturing apparatus illustrating a method for manufacturing a multi-layer oriented polyolefin film according to an embodiment.
- the multi-layer oriented polyolefin film (hereinafter also referred to as "oriented film” in brief) according to embodiments will be explained. Then, the method for manufacturing the multi-layer oriented polyolefin according to the embodiments will be explained.
- Figs. 3 and 4 are schematic structural views illustrating the multi-layer oriented polyolefin films according to embodiments.
- the oriented film may include at least two layers of multi-layer polyolefin film (F, also referred to as "multi-layer film” in brief), and a resin layer 40 laminated on the multi-layer film F.
- F multi-layer polyolefin film
- resin layer 40 laminated on the multi-layer film F.
- the multi-layer film F is obtained by laminating two or more layers via extrusion at the same time, wherein each layer includes at least polyolefin resin as a base resin (main material).
- the multi-layer film F may have a stack of 2 to 5 layers, more particularly 3 to 4 layers.
- the multi-layer film F may include a core layer 30, a skin outer layer 10 laminated on one side of the core layer 30, and a skin inner layer 20 laminated on the other side of the core layer 30.
- the multi-layer film F may have a tri-layer structure having the three layers, i.e., the skin outer layer 10, the core layer 30 and the skin inner layer 20, stacked successively, as shown in Figs. 3 and 4.
- each layer 10, 20, 30 may include, as a base resin (main material), at least one resin selected from the group consisting of polypropylene (PP) and polyethylene (PE).
- PP polypropylene
- PE polyethylene
- the skin outer layer 10 and the core layer 30 may be a PP layer having PP as a base resin.
- the skin inner layer 20 may be formed of PP layer, PE layer or PP-PE composite layer, each having PP, PE, or PP-PE composite as a base resin.
- the oriented film includes a resin layer 40 laminated on the multi-layer film F.
- the resin layer 40 may be formed as one layer or two layers and be laminated on at least one of the skin outer layer 10 and the skin inner layer 20.
- Fig. 3 shows that the resin layer 40 is laminated on the skin inner layer 20
- Fig. 4 shows that the resin layers 40 are laminated on both the skin outer layer 10 and the skin inner layer 20.
- the resin layer 40 is not formed by an additional coating process or a lamination process using hot-melting, but is laminated on the multi-layer film F through an extrusion process subsequent to machine direction orientation according to an embodiment.
- the method for manufacturing a multi-layer oriented polyolefin film will be explained in detail.
- Fig. 5 is a schematic view showing an apparatus for carrying out the method according to an embodiment.
- Fig. 5 is for illustrative purpose only, and various embodiments other than Fig. 5 may be made.
- the apparatus includes several devices of a first extruder 100-1, a first cooling roll 200, a machine direction orientation device 300, a second extruder 100-2, a second cooling roll 400, a transverse direction orientation device 500 and a winder 600. These devices are arranged so that a continuous process may be carried out. There is no particular limitation in particular structure of each devices.
- the machine direction orientation device 300 may include a combination of multiple rolls R as shown in Fig. 5.
- the reference numbers R1 and R2 represent guide rolls R1, R2 adjacent to the first cooling roll 200 and the second cooling roll 400, respectively.
- the method for manufacturing a multi-layer oriented polyolefin film includes carrying out a first extrusion molding to form a multi-layer polyolefin film F, first cooling the first extrusion molded film F, machine direction orienting the first cooled film F along the machine direction (i.e., longditudinal direction), carrying out a second extrusion molding to laminate at least one resin layer 40 on the machine direction oriented film F, second cooling the film F laminated with the resin layer 40, and transverse direction orienting the second cooled film F along the transverse direction. These steps of the method are carried out in a continuous manner.
- the multi-layer film F is extrusion-molded through a first extruder 100-1.
- the extrusion is carried out in such a manner that two or more layers are co-laminated, thereby providing the multi-layer film F.
- the first extruder 100-1 has extrusion sections in a number corresponding to the number of layers forming the multi-layer film F, and the layers are laminated at extrusion dies.
- the first extruder 100-1 may have three extrusion sections corresponding to the tri-layer structure.
- a polyolefin-based resin composition may be introduced to the first extruder 100-1.
- the polyolefin-based resin composition may include, as a base resin (main material), at least one polyolefin resin.
- a base resin main material
- at least one polyolefin resin there is no particular limitation on the polyolefin resin.
- at least one resin selected from PP and PE may be used.
- copolymer of at least one of ethylene and propylene particularly ethylene-methacrylic acid binary copolymer or ethylene-methacrylic acid-ester ternary copolymer, etc. may be used but not limited thereto.
- the polyolefin-based resin composition includes at least polyolefin resin and may further include other resins or additives if necessary.
- the polyolefin-based resin composition may include other resins or additives in an amount of 0 to 40 parts by weight, specifically 5 to 20 parts by weight based on 100 parts by weight of polyolefin resin.
- the additives are those generally used in the art and preferably examples thereof may include at least one selected from the group consisting of slip agents, anti-blocking agents, antistatic agents, etc. Particlur types of such additives will be described in detal hereinafter.
- the layers may be formed of the same or different materials.
- the skin outer layer 10 and the core layer 30 may be formed to be a PP layer, respectively by using PP as a base resin (main material).
- the skin inner layer 20 may be a PP layer, PE layer or a PP-PE composite layer by using PP, PE or PP-PE composite as a base resin (main material). It is prefreably that the skin inner layer 20 is a PE layer. Since PE layers have higher compatibility with a low-melting point resin such as ethylene vinyl acetate (EVA), etc. as compared to PP layers, PE layers may be preferable in preventing an interlayer separation.
- EVA ethylene vinyl acetate
- the outermost layer (skin outer layer 10) of the multi-layer film F when first extruding the multi-layer film F, it is preferable to extrude the outermost layer (skin outer layer 10) of the multi-layer film F to include at least one additive selected from slip agents and anti-blocking agents.
- the materials forming the skin outer layer 10 when the skin outer layer 10 has no resin layer 40 thereon and become the outermost layer of the final product (oriented film) as shown in Fig. 3, it is preferable for the materials forming the skin outer layer 10 to further include at least one additive selected from slip agents and anti-blocking agents.
- the slip agents are those capable of imparting slip property (or release property). Examples of such slip agents may include at least one selected from the group consisting of silicone, siloxane, silane, wax and oleic amide, etc. In addition to above-mentioned slip agents, any slip agents capable of imparting lubricability to the surface of the oriented film and reducing the frictional coefficient may be used.
- the slip agents may be used in, but not limited to, an amount of 0.1 to 20 parts by weight, specifically 2 to 12 parts by weight based on 100 parts by weight of polyolefin resin.
- the anti-blocking agents are those capable of preventing adhesion between two adjacent films by forming a small space at the interface of the adjacent films.
- Examples of the anti-blocking agents may include at least one selected from the group consisting of inorganic particles such as silica, diatomaceous earth, kaolin, talc, etc.
- the anti-blocking agents may be used in, but not limited to, the same amount as the slip agents, particularly in an amount of 0.1 to 20 parts by weight, specifically 2 to 12 parts by weight based on 100 parts by weight of polyolefin resin.
- the multi-layer film F has a tri-layer structure of the skin outer layer 10, core layer 30 and the skin inner layer 20, wherein the skin outer layer 10 may have a thickness T10 corresponding to 1 ⁇ 10% of the total thickness T of the oriented film, the core layer 30 may have a thickness T30 corresponding to 30 ⁇ 70% of the total thickness T of the oriented film, and the skin inner layer 20 may have a thickness T20 corresponding to 1 ⁇ 10% of the total thickness T of the oriented film.
- the first extrusion may be carried out at a various range of temperatures depending on the materials used for the first extrusion. For example, the first extrusion may be carried out at a temperature of 140 ⁇ 320°C.
- the extrusion molded multi-layer film F through the first extrusion molding is then passed through a first cooling roll 200 so that it may be cooled (first coolng).
- a first cooling roll 200 shows one cooling roll 200 in the manufacturing apparatus, one, two or more cooling rolls 200 may be arranged continuously in the appratus.
- the cooling temperature i.e., the temperature of the first cooling roll 200 may be, but not limited to, 5 ⁇ 80°C.
- the first cooled multi-layer film F is transferred to a machine direction orientation device 300 along a guide roll R1 so that it is oriented along the machine direction (i.e., longitudinal direction).
- the machine direction orientation MDO
- the machine direction orientation may be carried out through a plurality of rolls R.
- the orientation temperature of this mchine direction orientation step i.e., the temperature of the rolls R installed in the machine direction orientation device 300 may be, but not limited to, 80 ⁇ 160°C.
- the machine direction orientation may be carried out at an orientation ratio of 1.5 to 10 times, particularly 3 to 7 times, and more particularly 4 to 5 times.
- the ratio of the machine direction orientation may be realized by the speed of rolls R.
- the multi-layer film F is further subjected to additional extrusion (second extrusion) and cooling (second cooling) continuously.
- second extrusion additional extrusion
- second cooling second cooling
- a resin layer 40 is laminated on the multi-layer film F.
- the machine direction oriented multi-layer film F is supplied to a second extruder 100-2.
- the second extruder 100-2 may have a resin feed section 150 from which materials forming the resin layer 40 are supplied.
- the multi-layer film F is passed through the second extruder 100-2, and the materials forming the resin layer are supplied from the resin feed section 150 at the same time. In this manner, while the resin layer 40 is extruded, the resin layer 40 is laminated on the multi-layer film F at the dies.
- the materials forming the resin layer 40 i.e. the materials supplied from the resin feed section 150 to the second extruder 100-2 are not particularly limited.
- examples of the materials of the resin layer 40 may include at least one selected from the group consisting of polyolefin resins, silicone resins, urethane resins, acrylic resins, polyamide resins, metallocene resins, nylon resins, ethylene vinyl acetate (EVA), ethylene methyl acetate (EMA), ethylene methyl acrylic acid (EMAA), ethylene glycol (EG), ethylene acid terpolymer and rubber.
- the transverse direction orientation is not carried out right after the machine direction orientation. Rather, the resin layer 40 is laminated through the additional extrusion, i.e., the second extrusion.
- the resin layer 40 is laminated through the additional extrusion, i.e., the second extrusion.
- materials having physicochemical properties different from those of the base resin forming the multi-layer film F as for the resin layer 40 (e.g. materials having a lower or higher melting point than polyolefin, etc.).
- resins other than polyolefin, more particularly functional resins having a lower or higher melting point than polyolefin, as for the resin layer 40 are used as materials for the resin layer 40.
- materials including a resin having a lower melting point than the materials used for the first extrusion may be used as materials for the resin layer 40.
- low-temperature adhesive resins capable of hot-melting (heat sealing) at low temperature may be used.
- resins having a low melting point and high sealability such as EVA, EMA, EMMA, low-temperature metallocene resins and ethylene acid terpolymer may be used as for the low-temperature adhesive resins.
- the ethylene acid terpolymer may be useful when the oriented film is applied to in-mold labels, and examples of the ethylene acid terpolymer may include ethylene/propylene/butadiene terpolymer, etc.
- examples of commercially available terpolymer products include appeel® 52009 available from DuPont Co.
- the low-melting point resins as materials for the resin layer 40 are not limited to the above listed resins, and PE may also be used.
- PE when PP is used as the base resin of the skin outer layer 10 and/or skin inner layer 20, PE having a lower melting point than PP may be used as the resin forming the resin layer 40.
- the resin layer 40 is laminated through the second extrusion.
- the resin layer 40 may include materials containing an antistatic agent.
- the resin layer 40 becomes an antistatic layer.
- the antistatic agent may be a permanent antistatic agent with no change in antistatic quality as time goes.
- the antistatic agent may provide the oriented film with a surface resistance of 10 10 ⁇ /cm2 or less.
- the antistatic agent may include polyamide resin or ethylene glycol (EG), and commercial product such as IRAGASTT® P18 (Ciba, Germany) may be used as the antistatic agent.
- the antistatic agent may be selected from conductive polymers. Examples of the conductive polymers may include at least one selected from the group consisting of polyacetylene, poly(p-phenylene vinylene), poly(p-phenylene), poly(thienylene vinylene), polythiophene, polyaniline, polyethylene dioxythiophene, polyisothianaphthene, polypyrrole and poly(p-phenylene sulfide).
- the antistatic agent may be used in the materials of the resin layer 40 to impart the antistatic property. Otherwise, a master batch containing the antistatic agents may be used for the resin layer 40. For example, a master batch based on PP or PE and further containing an adequate amount of antistatic agent may be used for the resin layer 40.
- the oriented film may be useful as a packaging material for electronic appliances, etc. In order to make the oriented film more useful as a packaging material for electronic appliances, etc., it is preferable that the oriented film have a surface resistance of 10 10 ⁇ /cm2 or less by using the resin layer 40 containing the antistatic agents.
- the antistatic agent is a resin having a low molecular weight and low melting point, it may be exuded toward the surface of the film F as time goes.
- the antistatic agent may be exuded during the machine direction orientation, resulting in contamination of the surface of the rolls R.
- the surface of the film F may also be contaminated (whitening).
- antistatic property may also be degraded.
- an antistatic agent is contained in the resin layer 40 during the second extrusion (in-line extrusion) subsequent to the machine direction orientation, and thus it becomes possible to overcome the above-mentioned problems. That is, according to an embodiment, an antistatic agent is contatined in the resin layer 40 through the second additional extrusion after the machine direction orientation, and thus may not cause the contamination of the surface of rolls R of the machine direction orientation device 300 or the surface of the film F. Therefore, it is possible to realize stable antistatic property without the loss of the antistatic agent.
- the materials of the resin layer 40 may include a nylon resin.
- the resin layer 40 may be a nylon resin layer containing a nylon resin as a main material.
- the oriented film may be useful as a packaging material for food by virtue of excellent gas barrier property of nylon resin.
- nylon resins have an excellent low-temperature resistance, and thus may be useful for packaging of frozen food. Any nylon resin having an amide bond (-CONH) in its molecule may be used herein.
- the nylon resin may include any one selected from the group consisting of Nylon 6, Nylon 66 and Nylon 12, or a combination thereof (e.g. Nylon 6 + Nylon 66, Nylon 6 + Nylon 12, Nylon 6 + Nylon 66 + Nylon 12).
- a resin composition having the above-mentioned resin as a main material and further containing other additives may be used for the resin layer 40.
- used for the resin layer 40 is a resin composition containing at least one base resin selected from the group consisting of low-melting point adhesive resins, such as ethylene vinyl acetate (EVA), ethylene methyl acetate (EMA), ethylene methyl acrylic acid (EMAA), low-temperature metallocene resin and ethylene acid terpolymer; antistatic resins (antistatic agents) such as polyamide resins, ethylene glycol (EG) and conductive polymers; and resins having gas-barrier property and low-temperature resistace, such as nylon resins; optionally further in combination with at least one additive selected from the group consisting of slip agent, anti-blocking agent, etc.
- low-melting point adhesive resins such as ethylene vinyl acetate (EVA), ethylene methyl acetate (EMA), ethylene methyl acrylic acid (EMAA), low-temperature metallocene resin and
- the slip agent may be used in an amount of 0.1 to 20 parts by weight, specifically 2 to 12 parts by weight based on 100 parts by weight of the base resin.
- the anti-blocking agent may be used in an amount of 0.1 to 20 parts by weight, specifically 2 to 12 parts by weight based on 100 parts by weight of the base resin.
- the resin layer 40 may be formed to have a thickness T40 corresponding to 1 ⁇ 50% of the total thickness T of the oriented film.
- the extrusion temperature in the second extrusion may be decided considering the materials of the resin layer 40, i.e., the particular type and melting point of the base resin forming the resin layer 40.
- the second extrusion temperature may be 150 ⁇ 330°C.
- the second extrusion temperature is lower than 150°C, it may be difficult to perform the second extrusion.
- the second extrusion temperature is higher than 330°C, it may cause undesirably high flowability.
- the multi-layer film F laminated with the resin layer 40 via the second extrusion is passed continuously through a second cooling roll 400 so that it undergoes the second cooling.
- the second cooling is carried out in such a manner that the resin layer 40 is in close contact with the roll surface of the second cooling roll 400.
- Fig. 5 shows only one cooling roll 400 in the apparatus, one or more cooling rolls 400 may be disposed continuously in the apparatus.
- the cooling temperature in the second cooling i.e., the temperature of the second cooling roll 400 may be set as, but not limited to, 5 ⁇ 80°C.
- air flow grooves be formed on the resin layer 40 when the resin layer 40 is cooled in the second cooling.
- Such air flow grooves may improve the winding quality of the film.
- the transverse direction oriented film is wound at a winder 600, it may be wrinkled during the winding and may not be restored with ease.
- the resin layer 40 is not formed by the conventional coating process as used in the related art but is laminated through the continuous second extrusion after the machine direction orientation, it may be wrinkled during winding. When a low-melting point material is used for the resin layer 40, more wrinkling may occur.
- the air flow grooves may provide air flow paths to prevent such wrinkling effectively during winding. That is, the air flow grooves may effectively prevent the wrinkling by allowing air present between two adjacent films to be discharged through the air flow grooves.
- Multiple air flow grooves may be formed and there is no particular limitation in the shapes of the air flow grooves.
- the air flow grooves may be formed on the surface of the resin layer 40 along the longitudinal direction or widthwise direction, for example, in a linear pattern or lattice-like pattern, or in an embossed pattern, in a regular or irregular manner.
- the air flow grooves are formed during the second cooling.
- a second cooling roll 400 having an uneven structure (engraved structure) on the surface thereof may be used to form the air flow grooves.
- a cooling roll engraved to have an embossed surface 450 is used as the second cooling roll 400 so that air flow grooves may be formed on the resin layer 40.
- the resin layer 40 is allowed to be in close contact with the second cooling roll 400 having the embossed surface 450 so that air flow grooves are formed on the resin layer 40.
- the uneven structure formed on the second cooling roll there is no particular limitation in shapes and structures of the uneven structure formed on the second cooling roll as long as the uneven structure may form the air flow grooves, and various designs may be used.
- the uneven structure may be formed in a linear or lattice-like pattern parallel or perpendicular to the axial direction of the second cooling roll 400.
- the uneven structure may be formed in a regular or irregular embossed pattern protruding from the surface of the second cooling roll 400.
- the air flow grooves may be removed easily when the oriented film is converted into a commercial product or is used.
- the oriented film wound at a winder 600 may be cut into a desired size to be a product.
- an application of heat to the oriented film allow an easy removal of the air flow grooves.
- the air flow grooves may be removed and the oriented film may maintain its smoothness.
- the air flow grooves may be removed easily while the oriented film is used.
- the oriented film may be used for packaging, labels and lamination coating (laminated sheets).
- the air flow grooves may be removed with ease by the heat.
- the second cooled film is transferred to a transverse direction orientation device 500 along guide rolls R2 so that it is oriented along the widthwise direction (TDO).
- TDO widthwise direction
- any conventional transverse direction orientation device may be used for the purose.
- the transverse direction orientation may be carried out by setting the temperature of the transverse direction orientation device 500 at 100 ⁇ 200°C, but is not limited thereto.
- the transverse direction orientation may be carried out at an orientation ratio of 2 ⁇ 15 times, particularly 5 ⁇ 12 times, and more particularly 5 ⁇ 10 times. Such a transverse direction orientation ratio may be realized by a rail pattern.
- the transverse direction oriented film is wound at the winder 600 and then is made as a product.
- the film is subjected to trimming as usual before it is wound. Particularly, when both ends of the film have a difference in thickness after the film is passed through the transverse direction orientation device 500, trimming may be carried out to remove the both ends, and then the film is wound at the winder 600.
- the transverse direction orientation is not carried out right after the machine direction orientation. Rather, the second extrusion and second cooling are included between the transverse direction orientation and the machine direction orientation.
- the resin layer 40 is laminated through the second extrusion so that even a resin having a low melting point may be extruded and laminated.
- a multi-layer oriented film having a resin layer 40 may be obtained through the continuous extrusion. In this manner, it is possible to simplify the manufacturing process, and thereby reducing time and cost.
- a second cooling roll 400 having an uneven structure on its surface 450 during the second cooling it is possible to prevent wrinkling by virtue of the air flow grooves formed on the resin layer 40, and thus to improve the appearance of the multi-layer film.
- the resin layer 40 has excellent interlayer adhesion strength to the film F, and particularly has adhesion strength equal to or higher than the strength that may be obtained by the conventional coating process.
- the oriented film according to the embodiments may be useful for various packaging materials, labels, lamination coating (laminated sheets), or the like.
- the oriented film may be used as a packaging material for food, electronic appliances and medical products, as lamination coating (laminated sheets) for ID documents, printed matters, menu boards, etc., and as a label adhesion.
- a multi-layer oriented polyolefin film obtained by the above-described method.
- the multi-layer oriented polyolefin film has the same structure and layers as described above.
- test about the interlayer adhesion strength (adhesive force) of the extruded film according to the examples as compared to a conventional coating film will be described.
- the test is provided to evaluate the interlayer adhesion strength (adhesive force) between the resin layer 40 and the skin inner layer 20.
- the apparatus as shown in Fig. 5 is used to form a skin outer layer 10/core layer 30/skin inner layer 20 via extrusion, followed by cooling and machine direction orientation at an orientation ratio of 4 times.
- an EVA layer as a resin layer 40 is laminated on the skin inner layer 20 through an in-line process of continuous extrusion, followed by cooling and transverse direction orientation at an orientation ratio of 8 times.
- a tetra-layer structured oriented film as shown in Fig. 3 is prepared.
- the skin outer layer 10 and the core layer 30 are PP layers and the skin inner layer 20 is a PE layer (Example 1).
- Example 2 a paper is thermally laminated on the EVA layer.
- a commercially available thermally laminated EVA product is used as a sample for Comparative Examples 1 and 2.
- a skin outer layer (PP layer)/core layer (PP layer)/skin inner layer (PE layer) is formed via extrusion and cooled, followed by machine direction orientation at an orientation ratio of 4 tiems and transverse direction orientation at an orientation ratio of 8 times. The machine direction orientation and transverse direction orientation are carried out continuously.
- an EVA layer is thermally laminated on the skin inner layer (PE layer) through an off-line process, and the resultant multi-layer film is used as Comparative Example 1.
- a paper is thermally laminated on the EVA layer, and the resultant multi-layer film is used as Comparative Example 2.
- Example 1 Each sample according to Example 1 and Comparative Example 1 is evaluated in terms of interlayer adhesion strength, and the results are shown in the following Table 1.
- Each sample is cut into a size of 15 mm X 150 mm (width X length) by using a cutter bar.
- the electrolyte container having the sample is stored in a drying oven at 85°C for 1 day.
- the sample is removed from the container and the interlayer adhesion strength (peel strength) is determined by using a tensile strength tester at an angle of 180 ⁇ .
- Example 2 The samples according to Example 2 and Comparative Example 2 are evaluated in terms of the interlayer adhesion strength (peel strength) between the resin layer (EVA layer) and paper using the above-mentioned method. The results are also shown in the following Table 1.
- the multi-layer oriented film has an interlayer adhesion strength equal to or higher than that of the conventional thermally laminated film (Comparative Examples 1 and 2).
- each of the multi-layer oriented films of Examples 1 and 2 has excellent surface appearance.
- the paper-laminated multi-layer oriented film shows no coming off, when the paper-laminated multi-layer oriented film is folded. This suggests that the paper-laminated multi-layer oriented film has a good adhesion to the paper.
- This disclosure is directed to a method for manufacturing a multi-layer oriented polyolefin film, and a multi-layer oriented polyolefin film manufactured thereby.
- the method allows a simple process, thereby reducing time and cost.
Landscapes
- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Chemical & Material Sciences (AREA)
- Physics & Mathematics (AREA)
- Thermal Sciences (AREA)
- Manufacturing & Machinery (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Health & Medical Sciences (AREA)
- Materials Engineering (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Laminated Bodies (AREA)
- Extrusion Moulding Of Plastics Or The Like (AREA)
- Shaping By String And By Release Of Stress In Plastics And The Like (AREA)
- Manufacture Of Macromolecular Shaped Articles (AREA)
Abstract
This disclosure is directed to a method for manufacturing a multi-layer oriented polyolefin film, and a multi-layer oriented polyolefin film obtained thereby. In the method, a machine direction orientation after an extrusion is followed by an additional extrusion, wherein the additional extrusion allows lamination of a resin layer so that even a low-melting point resin may be laminated via the continuous extrusion. Accordingly, the method allows a simple process, thereby reducing time and cost.
Description
This disclosure relates to a method for manufacturing a multi-layer oriented polyolefin film, and a multi-layer oriented polyolefin film manufactured thereby.
In general, multi-layer oriented polyolefin films, such as polypropylene (PP) or polyethylene (PE) films, have been widely used in packaging materials or lamination coating (laminated sheets). In addition to the PP and PE films, there have been used polyvinyl chloride (PVC) films or polyethylene terephthalate (PET) films. However, PVC films may emit harmful materials, such as dioxin, upon incineration, and PET films may not be cost-efficient and have a difficulty in recycling.
Therefore, multi-layer oriented polyolefin films advantageous in terms of cost-efficiency and recyclability, particularly multi-layer biaxially oriented polypropylene (BOPP) films have been used more frequently. Such BOPP films are advantageous in terms of cost-efficiency and recyclability, and also have an excellece in mechanical properties such as tensile strength, rigidity, surface hardness and impact resistance, optical properties such as gloss and transparency, and food hygiene characteristics such as non-toxicity and odorless characteristics. Thus, they are useful for packaging materials (food packaging, etc.) or lamination coating (laminated sheets).
Fig. 1 is a schematic structural view of a conventional general BOPP film, and Fig. 2 is a schematic view illustrating a method for manufacturing a BOPP film according to the related art.
Referring to Fig. 1, a BOPP film generally includes a PP layer as a core layer 3, and a skin outer layer 1 and a skin inner layer 2 stacked on one side and the other side of the core layer 3, respectively. Herein, the skin outer layer 1 comprises PP, while the skin inner layer 2 comprises PP or PE. In addition, a functional resin layer 4 may be stacked on the skin outer layer 1 and/or skin inner layer 2.
For example, when such a BOPP film is used for lamination coating (laminated sheets), particularly as a film for lamination coating (laminated sheets) wherein an identification matter such as a photograph, ID document, printed matter or menu board etc. are inserted between two sheets of BOPP films and then hot-melted, or as a packaging film (e.g. food packaging), the functional layer 4 may include a low-melting point adhesive resin such as ethylene vinyl acetate (EVA) or polyethylene (PE) capable of hot-melting (heat sealing).
In addition, referring to Fig. 2, when manufacturing the BOPP film having the above-described structure according to the related art, the skin outer layer 1, core layer 3 and the skin inner layer 2 are co-extruded through an extruder 5 so that the three layers 1, 2, 3 are laminated at extrusion dies. In this manner, it is possible to form a multi-layer film. Then, the extruded multi-layer film is passed through a cooling roll 6 so that it is cooled, and then is subjected to biaxial orientation, i.e., the machine direction orientation (MDO) and successive transverse direction orientation (TDO). In other words, as shown in Fig. 2, the extruded multi-layer film is passed through an machine direction orientation device 7 having multiple roll combinations R to carry out the orientation along the machine direction (i.e., longditudinal direction). Then, the machine direction oriented film is passed continuously to a transverse direction orientation device 8 to carry out the orientation along the transverse direction by way of a rail pattern. After that, the machine direction and transverse direction oriented film is wound at a winding roll 9.
As described above, a method for manufacturing a multi-layer BOPP film according to the related art includes extrusion, cooling, MD orientation and TD orientation so as to provide a multi-layer film having a structure of PP layer/PP layer/PP (or PE) layer as shown, for example, in Fig. 1.
In addition, after providing a multi-layer film through the above-described continuous process, a functional resin layer 4 is further laminated on the skin outer layer 1 and/or skin inner layer 2, as mentioned above. That is, in the method according to the related art, the functional resin layer 4 such as ethylene vinyl acetate (EVA), etc. is laminated through additional processes such as coating, lamination (hot-melting), etc. However, such additional processes are complicated and take much time and cost.
Herein, in order to carry out the lamination of the functional resin layer 4, a co-extrusion method including introducing the functional resin into the skin extrusion section upon the multi-layer extrusion coating may be contemplated. However, when there is a significant difference in physicochemical properties between the functional resin and polyolefin (e.g. PP), such co-extrusion may be difficult. That is, low-melting point resins or resins other than polyolefin resins are not amenable to the co-extrusion. For example, in the case of a low-melting point resin such as EVA, its melting point difference from PP causes degradation of interlayer adhesion strength (adhesive force). In addition, while the multi-layer film is passed through the rolls R of the MD orientation device 7, the resin layer 4 may be scratched, resulting in degradation of an appearance of the resultant product. Further, the resin layer 4 may be stuck to the rolls R, thereby making it difficult to carry out the co-extrusion.
To this end, the method for laminating a functional resin layer 4 according to the related art requires additional processes such as coating or lamination (hot-melting) which require a relatively long time and high cost, and as a result, cause an increase in manufacturing cost.
This disclosure is directed to providing a method for manufacturing a multi-layer oriented polyolefin film, which allows even a low-melting point functional resin to be laminated through a continuous process and allows a simple and time-efficient process to reduce a manufacturing cost of products. This disclosure is also directed to providing a multi-layer oriented polyolefin film obtained by the method.
In embodiments of the invention, provided ia a method for manufacturing a multi-layer oriented polyolefin film, including: carrying out a first extrusion molding of a multi-layer polyolefin film; first cooling the first extrusion molded film; machine direction orienting the first cooled film along the longditudinal direction; carrying out a second extrusion molding in order to laminate at least one resin layer on the machine direction oriented film; second cooling the film laminated with the resin layer; and transverse direction orienting the second cooled film along the transverse direction.
In an example embodiment, the second cooling of the film laminated with the resin layer may be carried out by using a cooling roll having an uneven structure on its surface to form air flow grooves on the resin layer.
In another embodiments of the invention, provided is a multi-layer oriented polyolefin film obtained by the above-described method.
According to embodiments of the method for manufacturing a multi-layer oriented polyolefin film, a machine direction orientation is followed by an additional extrusion/cooling (i.e., second extrusion/second cooling), wherein a resin layer is laminated through the additional extrusion. Thus, even a low-melting point resin may be laminated through the extrusion. In this manner, multiple layers, including a resin layer, may be laminated through such continuous extrusion to provide a multi-layer oriented polyolefin film. Accordingly, the method has a simple process, is time-efficient, and reduces the manufacture cost of products.
The above and other aspects, features and advantages of the disclosed embodiments will be more apparent from the following detailed description taken in conjunction with the accompanying drawings in which:
Fig. 1 is a schematic structural view of a general conventional biaxially oriented polypropylene (BOPP) film.
Fig. 2 is a schematic view of manufacturing apparatus illustrating a conventional method for manufacturing a BOPP film according to the related art;
Figs. 3 and 4 are schematic structural views illustrating the multi-layer oriented polyolefin films according to embodiments; and
Fig. 5 is a schematic view of manufacturing apparatus illustrating a method for manufacturing a multi-layer oriented polyolefin film according to an embodiment.
<Description of Numerals>
1: skin outer layer 2: skin inner layer
3: core layer 4: functional resin layer
5: extruder 6: cooling roll
7: machine direction orientation device
8: transverse direction orientation device
9: winding roll
10: skin outer layer 20: skin inner layer
30: core layer 40: resin layer
100-1: first extruder 100-2: second extruder
150: resin feed section 200: first cooling roll
300: machine direction orientation device
400: second cooling roll
500: transverse direction orientation device
600: winder
Example embodiments now will be described more fully hereinafter with reference to the accompanying drawings, in which example embodiments are shown. The present disclosure may, however, be embodied in many different forms and should not be construed as limited to the example embodiments set forth therein. Rather, these example embodiments are provided so that the present disclosure will be thorough and complete, and will fully convey the scope of the present disclosure to those skilled in the art. In the description, details of well-known features and techniques may be omitted to avoid unnecessarily obscuring the presented embodiments.
The terminology used herein is for the purpose of describing particular embodiments only and is not intended to be limiting of the present disclosure. As used herein, the singular forms "a", "an, "the" are intended to include the plural forms as well, unless the context clearly indicates otherwise. Furthermore, the use of the terms a, an, etc. does not denote a limitation of quantity, but rather denotes the presence of at least one of the referenced item.
It will be further understood that the terms "comprises" and/or "comprising" or "includes" and/or "including" when used in this specification, specify the presence of stated features, regions, integers, steps, operations, elements, and/or components, but do not preclude the presence or addition of one or more other features, regions, integers, steps, operations, elements, components, and/or groups thereof.
The multi-layer oriented polyolefin film (hereinafter also referred to as "oriented film" in brief) according to embodiments will be explained. Then, the method for manufacturing the multi-layer oriented polyolefin according to the embodiments will be explained.
Figs. 3 and 4 are schematic structural views illustrating the multi-layer oriented polyolefin films according to embodiments.
Referring to Fig. 3 and Fig. 4, the oriented film according to an embodiment may include at least two layers of multi-layer polyolefin film (F, also referred to as "multi-layer film" in brief), and a resin layer 40 laminated on the multi-layer film F.
Herein, the multi-layer film F is obtained by laminating two or more layers via extrusion at the same time, wherein each layer includes at least polyolefin resin as a base resin (main material). For example, the multi-layer film F may have a stack of 2 to 5 layers, more particularly 3 to 4 layers. In an examplel embodiment, the multi-layer film F may include a core layer 30, a skin outer layer 10 laminated on one side of the core layer 30, and a skin inner layer 20 laminated on the other side of the core layer 30.
In an example embodiment, the multi-layer film F may have a tri-layer structure having the three layers, i.e., the skin outer layer 10, the core layer 30 and the skin inner layer 20, stacked successively, as shown in Figs. 3 and 4. Herein, each layer 10, 20, 30 may include, as a base resin (main material), at least one resin selected from the group consisting of polypropylene (PP) and polyethylene (PE). More particularly, the skin outer layer 10 and the core layer 30 may be a PP layer having PP as a base resin. In addition, the skin inner layer 20 may be formed of PP layer, PE layer or PP-PE composite layer, each having PP, PE, or PP-PE composite as a base resin.
In addition, the oriented film includes a resin layer 40 laminated on the multi-layer film F. The resin layer 40 may be formed as one layer or two layers and be laminated on at least one of the skin outer layer 10 and the skin inner layer 20. Fig. 3 shows that the resin layer 40 is laminated on the skin inner layer 20, while Fig. 4 shows that the resin layers 40 are laminated on both the skin outer layer 10 and the skin inner layer 20.
As described below, the resin layer 40 is not formed by an additional coating process or a lamination process using hot-melting, but is laminated on the multi-layer film F through an extrusion process subsequent to machine direction orientation according to an embodiment. The method for manufacturing a multi-layer oriented polyolefin film will be explained in detail.
Fig. 5 is a schematic view showing an apparatus for carrying out the method according to an embodiment. Fig. 5 is for illustrative purpose only, and various embodiments other than Fig. 5 may be made.
Referring to Fig. 5, the apparatus includes several devices of a first extruder 100-1, a first cooling roll 200, a machine direction orientation device 300, a second extruder 100-2, a second cooling roll 400, a transverse direction orientation device 500 and a winder 600. These devices are arranged so that a continuous process may be carried out. There is no particular limitation in particular structure of each devices. For example, the machine direction orientation device 300 may include a combination of multiple rolls R as shown in Fig. 5. In Fig. 5, the reference numbers R1 and R2 represent guide rolls R1, R2 adjacent to the first cooling roll 200 and the second cooling roll 400, respectively.
The method for manufacturing a multi-layer oriented polyolefin film according to an embodiment includes carrying out a first extrusion molding to form a multi-layer polyolefin film F, first cooling the first extrusion molded film F, machine direction orienting the first cooled film F along the machine direction (i.e., longditudinal direction), carrying out a second extrusion molding to laminate at least one resin layer 40 on the machine direction oriented film F, second cooling the film F laminated with the resin layer 40, and transverse direction orienting the second cooled film F along the transverse direction. These steps of the method are carried out in a continuous manner.
In the first extrusion molding, the multi-layer film F is extrusion-molded through a first extruder 100-1. Particularly, the extrusion is carried out in such a manner that two or more layers are co-laminated, thereby providing the multi-layer film F. Herein, the first extruder 100-1 has extrusion sections in a number corresponding to the number of layers forming the multi-layer film F, and the layers are laminated at extrusion dies. For example, when a multi-layer film F having a tri-layer structure of a skin outer layer 10, core layer 30 and a skin inner layer 20 is to be formed, the first extruder 100-1 may have three extrusion sections corresponding to the tri-layer structure.
In addition, to perform the extrusion molding of the multi-layer film F, a polyolefin-based resin composition may be introduced to the first extruder 100-1. The polyolefin-based resin composition may include, as a base resin (main material), at least one polyolefin resin. There is no particular limitation on the polyolefin resin. Preferably, at least one resin selected from PP and PE may be used. In addition, as the polyolefin resin, copolymer of at least one of ethylene and propylene, particularly ethylene-methacrylic acid binary copolymer or ethylene-methacrylic acid-ester ternary copolymer, etc. may be used but not limited thereto.
Meanwhile, the polyolefin-based resin composition includes at least polyolefin resin and may further include other resins or additives if necessary. In a non-limiting example mbodiment, the polyolefin-based resin composition may include other resins or additives in an amount of 0 to 40 parts by weight, specifically 5 to 20 parts by weight based on 100 parts by weight of polyolefin resin. The additives are those generally used in the art and preferably examples thereof may include at least one selected from the group consisting of slip agents, anti-blocking agents, antistatic agents, etc. Particlur types of such additives will be described in detal hereinafter.
When providing the multi-layer film F through the first extrusion, the layers may be formed of the same or different materials. For example, as shown in Figs. 3 and 4, the skin outer layer 10 and the core layer 30 may be formed to be a PP layer, respectively by using PP as a base resin (main material). The skin inner layer 20 may be a PP layer, PE layer or a PP-PE composite layer by using PP, PE or PP-PE composite as a base resin (main material). It is prefreably that the skin inner layer 20 is a PE layer. Since PE layers have higher compatibility with a low-melting point resin such as ethylene vinyl acetate (EVA), etc. as compared to PP layers, PE layers may be preferable in preventing an interlayer separation.
In addition, when first extruding the multi-layer film F, it is preferable to extrude the outermost layer (skin outer layer 10) of the multi-layer film F to include at least one additive selected from slip agents and anti-blocking agents. Particularly, when the skin outer layer 10 has no resin layer 40 thereon and become the outermost layer of the final product (oriented film) as shown in Fig. 3, it is preferable for the materials forming the skin outer layer 10 to further include at least one additive selected from slip agents and anti-blocking agents.
The slip agents are those capable of imparting slip property (or release property). Examples of such slip agents may include at least one selected from the group consisting of silicone, siloxane, silane, wax and oleic amide, etc. In addition to above-mentioned slip agents, any slip agents capable of imparting lubricability to the surface of the oriented film and reducing the frictional coefficient may be used. The slip agents may be used in, but not limited to, an amount of 0.1 to 20 parts by weight, specifically 2 to 12 parts by weight based on 100 parts by weight of polyolefin resin.
The anti-blocking agents are those capable of preventing adhesion between two adjacent films by forming a small space at the interface of the adjacent films. Examples of the anti-blocking agents may include at least one selected from the group consisting of inorganic particles such as silica, diatomaceous earth, kaolin, talc, etc. The anti-blocking agents may be used in, but not limited to, the same amount as the slip agents, particularly in an amount of 0.1 to 20 parts by weight, specifically 2 to 12 parts by weight based on 100 parts by weight of polyolefin resin.
When providing the multi-layer film F through the first extrusion, it is preferable to control a thickness of each layer. For example, referring to Fig. 3, the multi-layer film F has a tri-layer structure of the skin outer layer 10, core layer 30 and the skin inner layer 20, wherein the skin outer layer 10 may have a thickness T10 corresponding to 1~10% of the total thickness T of the oriented film, the core layer 30 may have a thickness T30 corresponding to 30~70% of the total thickness T of the oriented film, and the skin inner layer 20 may have a thickness T20 corresponding to 1~10% of the total thickness T of the oriented film. In addition, the first extrusion may be carried out at a various range of temperatures depending on the materials used for the first extrusion. For example, the first extrusion may be carried out at a temperature of 140~320℃.
Referring to Fig. 5, the extrusion molded multi-layer film F through the first extrusion molding is then passed through a first cooling roll 200 so that it may be cooled (first coolng). Although Fig. 5 shows one cooling roll 200 in the manufacturing apparatus, one, two or more cooling rolls 200 may be arranged continuously in the appratus. The cooling temperature, i.e., the temperature of the first cooling roll 200 may be, but not limited to, 5~80℃.
Then, the first cooled multi-layer film F is transferred to a machine direction orientation device 300 along a guide roll R1 so that it is oriented along the machine direction (i.e., longitudinal direction). For example, as shown in Fig. 5, the machine direction orientation (MDO) may be carried out through a plurality of rolls R. The orientation temperature of this mchine direction orientation step, i.e., the temperature of the rolls R installed in the machine direction orientation device 300 may be, but not limited to, 80~160℃. In addition, the machine direction orientation may be carried out at an orientation ratio of 1.5 to 10 times, particularly 3 to 7 times, and more particularly 4 to 5 times. The ratio of the machine direction orientation may be realized by the speed of rolls R.
After the machine direction orientation, the multi-layer film F is further subjected to additional extrusion (second extrusion) and cooling (second cooling) continuously. During the second extrusion, a resin layer 40 is laminated on the multi-layer film F. Particularly, as shown in Fig. 5, the machine direction oriented multi-layer film F is supplied to a second extruder 100-2. Herein, the second extruder 100-2 may have a resin feed section 150 from which materials forming the resin layer 40 are supplied. The multi-layer film F is passed through the second extruder 100-2, and the materials forming the resin layer are supplied from the resin feed section 150 at the same time. In this manner, while the resin layer 40 is extruded, the resin layer 40 is laminated on the multi-layer film F at the dies.
In an embodiment, the materials forming the resin layer 40, i.e. the materials supplied from the resin feed section 150 to the second extruder 100-2 are not particularly limited. In the second extrusion, examples of the materials of the resin layer 40 may include at least one selected from the group consisting of polyolefin resins, silicone resins, urethane resins, acrylic resins, polyamide resins, metallocene resins, nylon resins, ethylene vinyl acetate (EVA), ethylene methyl acetate (EMA), ethylene methyl acrylic acid (EMAA), ethylene glycol (EG), ethylene acid terpolymer and rubber.
According to an embodiment, the transverse direction orientation is not carried out right after the machine direction orientation. Rather, the resin layer 40 is laminated through the additional extrusion, i.e., the second extrusion. Accodrdingly, it is possible to use materials having physicochemical properties different from those of the base resin forming the multi-layer film F as for the resin layer 40 (e.g. materials having a lower or higher melting point than polyolefin, etc.).
Particularly, in an embodiment, it is possible to use resins other than polyolefin, more particularly functional resins having a lower or higher melting point than polyolefin, as for the resin layer 40. Preferably, in the second extrusion, materials including a resin having a lower melting point than the materials used for the first extrusion may be used as materials for the resin layer 40. For example, low-temperature adhesive resins capable of hot-melting (heat sealing) at low temperature may be used. Particularly, resins having a low melting point and high sealability, such as EVA, EMA, EMMA, low-temperature metallocene resins and ethylene acid terpolymer may be used as for the low-temperature adhesive resins. Herein, the ethylene acid terpolymer may be useful when the oriented film is applied to in-mold labels, and examples of the ethylene acid terpolymer may include ethylene/propylene/butadiene terpolymer, etc. In addition, examples of commercially available terpolymer products include appeel® 52009 available from DuPont Co. The low-melting point resins as materials for the resin layer 40 are not limited to the above listed resins, and PE may also be used. For example, when PP is used as the base resin of the skin outer layer 10 and/or skin inner layer 20, PE having a lower melting point than PP may be used as the resin forming the resin layer 40.
As described above, according to an embodiment, the resin layer 40 is laminated through the second extrusion. Thus, there is no limitation in materials forming the resin layer 40, and the resin layer may have various functionalities. Preferably, in an embodiment, the resin layer 40 may include materials containing an antistatic agent. Herein, the resin layer 40 becomes an antistatic layer. There is no limitation in the antistatic agent as long as it has an antistatic property. Preferably, the antistatic agent may be a permanent antistatic agent with no change in antistatic quality as time goes. In addition, it is more preferable that the antistatic agent may provide the oriented film with a surface resistance of 1010 Ω/㎠ or less.
For example, the antistatic agent may include polyamide resin or ethylene glycol (EG), and commercial product such as IRAGASTT® P18 (Ciba, Germany) may be used as the antistatic agent. In addition, the antistatic agent may be selected from conductive polymers. Examples of the conductive polymers may include at least one selected from the group consisting of polyacetylene, poly(p-phenylene vinylene), poly(p-phenylene), poly(thienylene vinylene), polythiophene, polyaniline, polyethylene dioxythiophene, polyisothianaphthene, polypyrrole and poly(p-phenylene sulfide).
The antistatic agent may be used in the materials of the resin layer 40 to impart the antistatic property. Otherwise, a master batch containing the antistatic agents may be used for the resin layer 40. For example, a master batch based on PP or PE and further containing an adequate amount of antistatic agent may be used for the resin layer 40. When the resin layer 40 is provided with the antistatic property by having the antistatic agent in the resin layer 40, the oriented film may be useful as a packaging material for electronic appliances, etc. In order to make the oriented film more useful as a packaging material for electronic appliances, etc., it is preferable that the oriented film have a surface resistance of 1010 Ω/㎠ or less by using the resin layer 40 containing the antistatic agents.
Meanwhile, when imparting static electricity-preventing property (antistatic property) to the oriented film, a method for containing (adding) an antistatic agent to the multi-layer film F, for example, to the skin outer layer 10 or skin inner layer 20 may be contemplated. However, such a method has the problems as follows.
Since the antistatic agent is a resin having a low molecular weight and low melting point, it may be exuded toward the surface of the film F as time goes. Herein, when the multi-layer film F includes an antistatic agent, the antistatic agent may be exuded during the machine direction orientation, resulting in contamination of the surface of the rolls R. As a result, the surface of the film F may also be contaminated (whitening). In addition, due to the loss of antistatic agent (i.e., loss of antistatic agent attached to the surface of rolls R or film F), antistatic property may also be degraded.
However, according to an embodiment, an antistatic agent is contained in the resin layer 40 during the second extrusion (in-line extrusion) subsequent to the machine direction orientation, and thus it becomes possible to overcome the above-mentioned problems. That is, according to an embodiment, an antistatic agent is contatined in the resin layer 40 through the second additional extrusion after the machine direction orientation, and thus may not cause the contamination of the surface of rolls R of the machine direction orientation device 300 or the surface of the film F. Therefore, it is possible to realize stable antistatic property without the loss of the antistatic agent.
According to another embodiment, the materials of the resin layer 40 may include a nylon resin. In other words, the resin layer 40 may be a nylon resin layer containing a nylon resin as a main material. When the resin layer 40 includes a nylon resin, the oriented film may be useful as a packaging material for food by virtue of excellent gas barrier property of nylon resin. In addition, nylon resins have an excellent low-temperature resistance, and thus may be useful for packaging of frozen food. Any nylon resin having an amide bond (-CONH) in its molecule may be used herein. Examples of the nylon resin may include any one selected from the group consisting of Nylon 6, Nylon 66 and Nylon 12, or a combination thereof (e.g. Nylon 6 + Nylon 66, Nylon 6 + Nylon 12, Nylon 6 + Nylon 66 + Nylon 12).
Further, a resin composition having the above-mentioned resin as a main material and further containing other additives may be used for the resin layer 40. In an example embodiment, used for the resin layer 40 is a resin composition containing at least one base resin selected from the group consisting of low-melting point adhesive resins, such as ethylene vinyl acetate (EVA), ethylene methyl acetate (EMA), ethylene methyl acrylic acid (EMAA), low-temperature metallocene resin and ethylene acid terpolymer; antistatic resins (antistatic agents) such as polyamide resins, ethylene glycol (EG) and conductive polymers; and resins having gas-barrier property and low-temperature resistace, such as nylon resins; optionally further in combination with at least one additive selected from the group consisting of slip agent, anti-blocking agent, etc.
Particular types of the slip agent and anti-blocking agent are the same as described above. For example, the slip agent may be used in an amount of 0.1 to 20 parts by weight, specifically 2 to 12 parts by weight based on 100 parts by weight of the base resin. The anti-blocking agent may be used in an amount of 0.1 to 20 parts by weight, specifically 2 to 12 parts by weight based on 100 parts by weight of the base resin.
In addition, during the second extrusion, the resin layer 40 may be formed to have a thickness T40 corresponding to 1~50% of the total thickness T of the oriented film. Further, the extrusion temperature in the second extrusion may be decided considering the materials of the resin layer 40, i.e., the particular type and melting point of the base resin forming the resin layer 40. For example, the second extrusion temperature may be 150~330℃. When the second extrusion temperature is lower than 150℃, it may be difficult to perform the second extrusion. When the second extrusion temperature is higher than 330℃, it may cause undesirably high flowability. For example, when using a low-melting point resin, it is advantageous to carry out the second extrusion at 180~250℃.
Referring to Fig. 5, the multi-layer film F laminated with the resin layer 40 via the second extrusion is passed continuously through a second cooling roll 400 so that it undergoes the second cooling. When the multi-layer film F is passed through the second cooling roll 400, it is advantageous that the second cooling is carried out in such a manner that the resin layer 40 is in close contact with the roll surface of the second cooling roll 400. Although Fig. 5 shows only one cooling roll 400 in the apparatus, one or more cooling rolls 400 may be disposed continuously in the apparatus. The cooling temperature in the second cooling, i.e., the temperature of the second cooling roll 400 may be set as, but not limited to, 5~80℃.
In an embodiment, it is preferabe that air flow grooves be formed on the resin layer 40 when the resin layer 40 is cooled in the second cooling. Such air flow grooves may improve the winding quality of the film. As described below, when the transverse direction oriented film is wound at a winder 600, it may be wrinkled during the winding and may not be restored with ease. Since the resin layer 40 is not formed by the conventional coating process as used in the related art but is laminated through the continuous second extrusion after the machine direction orientation, it may be wrinkled during winding. When a low-melting point material is used for the resin layer 40, more wrinkling may occur.
The air flow grooves may provide air flow paths to prevent such wrinkling effectively during winding. That is, the air flow grooves may effectively prevent the wrinkling by allowing air present between two adjacent films to be discharged through the air flow grooves. Multiple air flow grooves may be formed and there is no particular limitation in the shapes of the air flow grooves. The air flow grooves may be formed on the surface of the resin layer 40 along the longitudinal direction or widthwise direction, for example, in a linear pattern or lattice-like pattern, or in an embossed pattern, in a regular or irregular manner.
In an example embodiment, the air flow grooves are formed during the second cooling. Herein, a second cooling roll 400 having an uneven structure (engraved structure) on the surface thereof may be used to form the air flow grooves. Particularly, as shown in Fig. 5, a cooling roll engraved to have an embossed surface 450 is used as the second cooling roll 400 so that air flow grooves may be formed on the resin layer 40. In other words, when the multi-layer film F laminated with the resin layer 40 from the second extrusion is passed and cooled through the second cooling roll 400, the resin layer 40 is allowed to be in close contact with the second cooling roll 400 having the embossed surface 450 so that air flow grooves are formed on the resin layer 40. There is no particular limitation in shapes and structures of the uneven structure formed on the second cooling roll as long as the uneven structure may form the air flow grooves, and various designs may be used. For example, the uneven structure may be formed in a linear or lattice-like pattern parallel or perpendicular to the axial direction of the second cooling roll 400. In an example, the uneven structure may be formed in a regular or irregular embossed pattern protruding from the surface of the second cooling roll 400.
The air flow grooves may be removed easily when the oriented film is converted into a commercial product or is used. Particularly, the oriented film wound at a winder 600 may be cut into a desired size to be a product. Herein, an application of heat to the oriented film allow an easy removal of the air flow grooves. In other words, when the oriented film is heated to a desired temperature, the air flow grooves may be removed and the oriented film may maintain its smoothness. In addition, the air flow grooves may be removed easily while the oriented film is used. For example, the oriented film may be used for packaging, labels and lamination coating (laminated sheets). Herein, when the oriented film is heated for sealing or coating adhesion, the air flow grooves may be removed with ease by the heat.
Referring to Fig. 5, the second cooled film is transferred to a transverse direction orientation device 500 along guide rolls R2 so that it is oriented along the widthwise direction (TDO). Herein, any conventional transverse direction orientation device may be used for the purose. The transverse direction orientation may be carried out by setting the temperature of the transverse direction orientation device 500 at 100~200℃, but is not limited thereto. In addition, the transverse direction orientation may be carried out at an orientation ratio of 2~15 times, particularly 5~12 times, and more particularly 5~10 times. Such a transverse direction orientation ratio may be realized by a rail pattern.
As mentioned above, the transverse direction oriented film is wound at the winder 600 and then is made as a product. After the transverse direction orientation, the film is subjected to trimming as usual before it is wound. Particularly, when both ends of the film have a difference in thickness after the film is passed through the transverse direction orientation device 500, trimming may be carried out to remove the both ends, and then the film is wound at the winder 600.
According to the embodiments described above, the transverse direction orientation is not carried out right after the machine direction orientation. Rather, the second extrusion and second cooling are included between the transverse direction orientation and the machine direction orientation. The resin layer 40 is laminated through the second extrusion so that even a resin having a low melting point may be extruded and laminated. A multi-layer oriented film having a resin layer 40 may be obtained through the continuous extrusion. In this manner, it is possible to simplify the manufacturing process, and thereby reducing time and cost. Further, when using a second cooling roll 400 having an uneven structure on its surface 450 during the second cooling, it is possible to prevent wrinkling by virtue of the air flow grooves formed on the resin layer 40, and thus to improve the appearance of the multi-layer film. In addition, the resin layer 40 has excellent interlayer adhesion strength to the film F, and particularly has adhesion strength equal to or higher than the strength that may be obtained by the conventional coating process.
The oriented film according to the embodiments may be useful for various packaging materials, labels, lamination coating (laminated sheets), or the like. For example, the oriented film may be used as a packaging material for food, electronic appliances and medical products, as lamination coating (laminated sheets) for ID documents, printed matters, menu boards, etc., and as a label adhesion.
In an embodiment, provided is a multi-layer oriented polyolefin film obtained by the above-described method. The multi-layer oriented polyolefin film has the same structure and layers as described above.
The examples and comparative examples will now be described. Test about the interlayer adhesion strength (adhesive force) of the extruded film according to the examples as compared to a conventional coating film will be described. The test is provided to evaluate the interlayer adhesion strength (adhesive force) between the resin layer 40 and the skin inner layer 20.
[Examples 1 and 2]
The apparatus as shown in Fig. 5 is used to form a skin outer layer 10/core layer 30/skin inner layer 20 via extrusion, followed by cooling and machine direction orientation at an orientation ratio of 4 times. After the machine direction orientation, an EVA layer as a resin layer 40 is laminated on the skin inner layer 20 through an in-line process of continuous extrusion, followed by cooling and transverse direction orientation at an orientation ratio of 8 times. In this manner, a tetra-layer structured oriented film as shown in Fig. 3 is prepared. Herein, the skin outer layer 10 and the core layer 30 are PP layers and the skin inner layer 20 is a PE layer (Example 1). In Example 2, a paper is thermally laminated on the EVA layer.
[Comparative Examples 1 and 2]
A commercially available thermally laminated EVA product is used as a sample for Comparative Examples 1 and 2. Particularly, a skin outer layer (PP layer)/core layer (PP layer)/skin inner layer (PE layer) is formed via extrusion and cooled, followed by machine direction orientation at an orientation ratio of 4 tiems and transverse direction orientation at an orientation ratio of 8 times. The machine direction orientation and transverse direction orientation are carried out continuously. Then, an EVA layer is thermally laminated on the skin inner layer (PE layer) through an off-line process, and the resultant multi-layer film is used as Comparative Example 1. Meanwhile, a paper is thermally laminated on the EVA layer, and the resultant multi-layer film is used as Comparative Example 2.
Each sample according to Example 1 and Comparative Example 1 is evaluated in terms of interlayer adhesion strength, and the results are shown in the following Table 1.
Interlayer Adhesion Strength (Peel Strength)
(1) Each sample is cut into a size of 15 mm X 150 mm (width X length) by using a cutter bar.
(2) The resin layer (EVA layer) and the skin inner layer (PE layer) of the sample cut into a predetermined size are subjected to interlayer separation within a predetermined length by using a blade.
(3) The sample that has been subjected to interlayer separation within a predetermined length is dipped into a container in which a standard electrolyte is contained, followed by sealing (electrolyte: 1M LiPF6 solution).
(4) The electrolyte container having the sample is stored in a drying oven at 85℃ for 1 day.
(5) After 1 day, the sample is removed from the container and the interlayer adhesion strength (peel strength) is determined by using a tensile strength tester at an angle of 180˚.
(6) The samples according to Example 2 and Comparative Example 2 are evaluated in terms of the interlayer adhesion strength (peel strength) between the resin layer (EVA layer) and paper using the above-mentioned method. The results are also shown in the following Table 1.
Table 1 Results of Interlayer Adhesion Strength
Results | Ex.1 | Comp. Ex.1 | Ex.2 | Comp. Ex.2 |
Layered structure of the oriented film | PP/PP/PE/EVA | PP/PP/PE/EVA | PP/PP/PE/EVA/paper | PP/PP/PE/EVA/paper |
Method for forming EVA layer | In-line extrusion | Off-line thermal lamination | In-line extrusion | Off-line thermal lamination |
Interlayer adhesion strength (after 1 day) | 2.0 kgf | 1.5 kgf | 0.4 kgf | 0.4 kgf |
As shown in Table 1, when the resin layer (EVA layer) is laminated through the in-line extrusion according to the embodinents, the multi-layer oriented film has an interlayer adhesion strength equal to or higher than that of the conventional thermally laminated film (Comparative Examples 1 and 2). In addition, when evaluated by the naked eye, each of the multi-layer oriented films of Examples 1 and 2 has excellent surface appearance. Further, the paper-laminated multi-layer oriented film shows no coming off, when the paper-laminated multi-layer oriented film is folded. This suggests that the paper-laminated multi-layer oriented film has a good adhesion to the paper.
While the embodiments have been shown and described, it will be understood by those skilled in the art that various changes in form and details may be made thereto without departing from the spirit and scope of the present disclosure as defined by the appended claims. In addition, many modifications can be made to adapt a particular situation or material to the teachings of the present disclosure without departing from the essential scope thereof.
This disclosure is directed to a method for manufacturing a multi-layer oriented polyolefin film, and a multi-layer oriented polyolefin film manufactured thereby. The method allows a simple process, thereby reducing time and cost.
Claims (9)
- A method for manufacturing a multi-layer oriented polyolefin film, comprising:carrying out a first extrusion molding of a multi-layer polyolefin film;first cooling the first extrusion molded film;machine direction orienting the first cooled film along the longditudinal direction;carrying out a second extrusion molding in order to laminate at least one resin layer on the machine direction oriented film;second cooling the film laminated with the resin layer; andtransverse direction orienting the second cooled film along the transverse direction.
- The method according to claim 1, wherein the second cooling of the film laminated with the resin layer is carried out by using a cooling roll having an uneven structure on its surface to form air flow grooves on the resin layer.
- The method according to claim 1 or 2, wherein the first extrusion molding is carried out in such a manner that the film comprises a skin outer layer, a core layer and a skin inner layer, and the second extrusion molding is carried out in such a manner that a resin layer is laminated on at least one selected from the group consisting of the skin outer layer and the skin inner layer.
- The method according to claim 1 or 2, wherein a material comprising at least one selected from the group consisting of polyolefin resins, silicone resins, urethane resins, acrylic resins, polyamide resins, metallocene resins, nylon resins, ethylene vinyl acetate, ethylene methyl acetate, ethylene methyl acrylic acid, ethylene glycol, ethylene acid terpolymer and rubber is used for the resin layer in the second extrusion molding.
- The method according to claim 1 or 2, wherein a material comprising a resin having a lower melting point than a material used for the first extrusion molding is used for the resin layer in the second extrusion molding.
- The method according to claim 1 or 2, wherein a material comprising an antistatic agent is used for the resin layer in the second extrusion molding.
- The method according to claim 1 or 2, wherein a material comprising a nylon resin is used for the resin layer in the second extrusion molding.
- The method according to claim 3, wherein the first extrusion molding is carried out in such a manner that the skin outer layer comprises at least one selected from the group consisting of slip agent and anti-blocking agent.
- A multi-layer oriented polyolefin film manufactured by the method according to claim 1 or 2.
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2013548355A JP5807070B2 (en) | 2011-01-06 | 2012-01-06 | Method for producing a stretched multilayer polyolefin film including a heat seal resin layer |
IN1283MUN2013 IN2013MN01283A (en) | 2011-01-06 | 2012-01-06 | |
CN201280004677.1A CN103298600B (en) | 2011-01-06 | 2012-01-06 | Method for manufacturing a multi-layer oriented polyolefin film and multi-layer oriented polyolefin film manufactured thereby |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR1020110001452A KR101243463B1 (en) | 2011-01-06 | 2011-01-06 | Method for manufacturing oriented polyolefin film with multi-layer and oriented polyolefin film with multi-layer manufactured by thereof |
KR10-2011-0001452 | 2011-01-06 |
Publications (2)
Publication Number | Publication Date |
---|---|
WO2012093881A2 true WO2012093881A2 (en) | 2012-07-12 |
WO2012093881A3 WO2012093881A3 (en) | 2012-11-29 |
Family
ID=46457867
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/KR2012/000140 WO2012093881A2 (en) | 2011-01-06 | 2012-01-06 | Method for manufacturing a multi-layer oriented polyolefin film and multi-layer oriented polyolefin film manufactured thereby |
Country Status (5)
Country | Link |
---|---|
JP (2) | JP5807070B2 (en) |
KR (1) | KR101243463B1 (en) |
CN (1) | CN103298600B (en) |
IN (1) | IN2013MN01283A (en) |
WO (1) | WO2012093881A2 (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2018160144A1 (en) * | 2017-03-03 | 2018-09-07 | Vitray Plasti̇k Ambalaj San. Ve Ti̇c. A. Ş. | Food-safety high plastic piping bag having outer, inner and middle layer |
WO2019224838A1 (en) * | 2018-05-19 | 2019-11-28 | Huhtamaki-Ppl Limited | A laminate |
RU2712874C2 (en) * | 2014-04-09 | 2020-01-31 | Секисуй Кемикал Ко., Лтд. | Vehicle windshield intermediate film, coiled article and windshield glass of vehicle |
US11565507B2 (en) | 2014-04-09 | 2023-01-31 | Sekisui Chemical Co., Ltd. | Laminated-glass intermediate film, rolled body, laminated glass, and method for producing laminated glass |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2015046984A1 (en) * | 2013-09-30 | 2015-04-02 | 코오롱인더스트리 주식회사 | Film for laminating metal plate |
KR102145946B1 (en) | 2019-09-25 | 2020-08-19 | 호림판매(주) | Method for manufacturing packaging material using opaque monolayer film and packaging material to form a structure for easy identification of contents using monolayer film manufactured thereby |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR19990016889A (en) * | 1997-08-20 | 1999-03-15 | 장용균 | Method of producing polypropylene film |
KR19990052885A (en) * | 1997-12-23 | 1999-07-15 | 장용균 | Method for producing white biaxially oriented three-layer polypropylene film |
KR19990066441A (en) * | 1998-01-26 | 1999-08-16 | 장용균 | Manufacturing method of heat-adhesive extrusion coated biaxially stretched polyolefin film |
KR20100040460A (en) * | 2008-10-10 | 2010-04-20 | 주식회사 에스케이지플라스텍 | Heat-shinkable multi-layer olefin film for packaging the products |
Family Cites Families (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6042025A (en) * | 1983-08-18 | 1985-03-06 | Oji Yuka Gouseishi Kk | Manufacture of composite polypropylene resin stretched film |
DE3824286A1 (en) * | 1988-07-16 | 1990-02-08 | Wolff Walsrode Ag | Multilayer film for coating substrate by contacting and applying heat |
JP2542427B2 (en) * | 1988-09-21 | 1996-10-09 | 王子油化合成紙株式会社 | Method for manufacturing synthetic paper for labels |
JPH085133B2 (en) * | 1989-08-04 | 1996-01-24 | 東レ株式会社 | Print laminating method |
JPH0999525A (en) * | 1995-10-05 | 1997-04-15 | Gunze Ltd | Thermal adhesive laminated polyolefinic film |
JP2001277352A (en) * | 1998-10-01 | 2001-10-09 | Nippon Synthetic Chem Ind Co Ltd:The | Method for manufacturing laminate |
JP4822589B2 (en) * | 2000-12-26 | 2011-11-24 | 株式会社ユポ・コーポレーション | In-mold label |
EP1369220A4 (en) * | 2001-02-22 | 2004-04-21 | Yupo Corp | Label for in-mold forming |
JP5292819B2 (en) * | 2008-01-15 | 2013-09-18 | 東レ株式会社 | Method for producing a polyolefin film for surface protection |
-
2011
- 2011-01-06 KR KR1020110001452A patent/KR101243463B1/en active IP Right Grant
-
2012
- 2012-01-06 JP JP2013548355A patent/JP5807070B2/en active Active
- 2012-01-06 WO PCT/KR2012/000140 patent/WO2012093881A2/en active Application Filing
- 2012-01-06 CN CN201280004677.1A patent/CN103298600B/en active Active
- 2012-01-06 IN IN1283MUN2013 patent/IN2013MN01283A/en unknown
-
2015
- 2015-03-05 JP JP2015043255A patent/JP2015155202A/en active Pending
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR19990016889A (en) * | 1997-08-20 | 1999-03-15 | 장용균 | Method of producing polypropylene film |
KR19990052885A (en) * | 1997-12-23 | 1999-07-15 | 장용균 | Method for producing white biaxially oriented three-layer polypropylene film |
KR19990066441A (en) * | 1998-01-26 | 1999-08-16 | 장용균 | Manufacturing method of heat-adhesive extrusion coated biaxially stretched polyolefin film |
KR20100040460A (en) * | 2008-10-10 | 2010-04-20 | 주식회사 에스케이지플라스텍 | Heat-shinkable multi-layer olefin film for packaging the products |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
RU2712874C2 (en) * | 2014-04-09 | 2020-01-31 | Секисуй Кемикал Ко., Лтд. | Vehicle windshield intermediate film, coiled article and windshield glass of vehicle |
US11565507B2 (en) | 2014-04-09 | 2023-01-31 | Sekisui Chemical Co., Ltd. | Laminated-glass intermediate film, rolled body, laminated glass, and method for producing laminated glass |
WO2018160144A1 (en) * | 2017-03-03 | 2018-09-07 | Vitray Plasti̇k Ambalaj San. Ve Ti̇c. A. Ş. | Food-safety high plastic piping bag having outer, inner and middle layer |
WO2019224838A1 (en) * | 2018-05-19 | 2019-11-28 | Huhtamaki-Ppl Limited | A laminate |
Also Published As
Publication number | Publication date |
---|---|
CN103298600B (en) | 2017-02-15 |
JP2015155202A (en) | 2015-08-27 |
JP2014506208A (en) | 2014-03-13 |
KR101243463B1 (en) | 2013-03-13 |
KR20120080027A (en) | 2012-07-16 |
WO2012093881A3 (en) | 2012-11-29 |
CN103298600A (en) | 2013-09-11 |
JP5807070B2 (en) | 2015-11-10 |
IN2013MN01283A (en) | 2015-06-12 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
WO2012093881A2 (en) | Method for manufacturing a multi-layer oriented polyolefin film and multi-layer oriented polyolefin film manufactured thereby | |
CA2566479C (en) | Multilayer heat shrinkable film and wrapped battery | |
US7335274B2 (en) | Production method of decorative film | |
US6576325B1 (en) | Label | |
US8158250B2 (en) | Stretched film of void-containing thermoplastic resin and process for producing the same | |
WO2012030129A2 (en) | Multilayer film | |
WO2021194003A1 (en) | Multilayer polyethylene film and method for manufacturing same | |
JP6429175B2 (en) | Cover tape and manufacturing method thereof | |
JP4644548B2 (en) | Polyamide resin laminated film | |
EP0498249B1 (en) | Process for producing shrink film and resultant shrink film layers and laminates | |
WO2013012186A2 (en) | Method for manufacturing oriented polyolefin film and oriented polyolefin film manufactured therefrom | |
WO2021235650A1 (en) | Multilayer molded article with excellent tackiness and electrical conductivity and electronic product transported thereby | |
WO2021074931A1 (en) | Uv printable biaxially oriented polypropylene film and a method of manufacturing thereof | |
KR101924552B1 (en) | Easily separable heat shrinkable film | |
JP2020075375A (en) | Method for producing laminated sheet | |
EP4319982A1 (en) | Polyethylene film having multi-layer structure and packaging material produced using the same | |
WO2011002148A2 (en) | Heat-shrink film and method for manufacturing same | |
WO2023043010A1 (en) | Colorable conductive resin composition for preventing slips, and multilayer molded product comprising same | |
KR20230083830A (en) | Cover film for packaging electronic component and the electronic component packaging comprising the same | |
WO2023096140A1 (en) | Shrinkable labeling film having excellent transparency and printability | |
CN110757848A (en) | Method for manufacturing synthetic paper | |
JP4061425B2 (en) | Heat-shrinkable polystyrene resin film, label using the same, and container | |
KR20170038327A (en) | Co-extrusion film for cold forming |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
121 | Ep: the epo has been informed by wipo that ep was designated in this application |
Ref document number: 12732347 Country of ref document: EP Kind code of ref document: A2 |
|
ENP | Entry into the national phase |
Ref document number: 2013548355 Country of ref document: JP Kind code of ref document: A |
|
NENP | Non-entry into the national phase |
Ref country code: DE |
|
122 | Ep: pct application non-entry in european phase |
Ref document number: 12732347 Country of ref document: EP Kind code of ref document: A2 |