US3804663A - Method of internally coating rigid or semi-rigid plastic containers - Google Patents
Method of internally coating rigid or semi-rigid plastic containers Download PDFInfo
- Publication number
- US3804663A US3804663A US00147120A US14712071A US3804663A US 3804663 A US3804663 A US 3804663A US 00147120 A US00147120 A US 00147120A US 14712071 A US14712071 A US 14712071A US 3804663 A US3804663 A US 3804663A
- Authority
- US
- United States
- Prior art keywords
- coating
- article
- container
- heating
- parison
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 238000000576 coating method Methods 0.000 title claims abstract description 77
- 239000011248 coating agent Substances 0.000 title claims abstract description 68
- 238000000034 method Methods 0.000 title claims abstract description 68
- 229920003023 plastic Polymers 0.000 title abstract description 19
- 239000004033 plastic Substances 0.000 title abstract description 19
- 238000010438 heat treatment Methods 0.000 claims abstract description 35
- 239000006185 dispersion Substances 0.000 claims abstract description 27
- 239000004816 latex Substances 0.000 claims abstract description 24
- 229920000126 latex Polymers 0.000 claims abstract description 24
- 230000004888 barrier function Effects 0.000 claims abstract description 7
- 239000007788 liquid Substances 0.000 claims abstract description 6
- 229920000642 polymer Polymers 0.000 claims description 18
- 229920005989 resin Polymers 0.000 claims description 13
- 239000011347 resin Substances 0.000 claims description 13
- 238000000071 blow moulding Methods 0.000 claims description 11
- OEPOKWHJYJXUGD-UHFFFAOYSA-N 2-(3-phenylmethoxyphenyl)-1,3-thiazole-4-carbaldehyde Chemical compound O=CC1=CSC(C=2C=C(OCC=3C=CC=CC=3)C=CC=2)=N1 OEPOKWHJYJXUGD-UHFFFAOYSA-N 0.000 claims description 10
- 229920001577 copolymer Polymers 0.000 claims description 10
- 238000001035 drying Methods 0.000 claims description 10
- 239000000725 suspension Substances 0.000 claims description 10
- 238000007664 blowing Methods 0.000 claims description 7
- 239000000758 substrate Substances 0.000 claims description 7
- 239000000178 monomer Substances 0.000 claims description 5
- 239000003822 epoxy resin Substances 0.000 claims description 4
- 230000004927 fusion Effects 0.000 claims description 4
- 229920002239 polyacrylonitrile Polymers 0.000 claims description 4
- 229920000647 polyepoxide Polymers 0.000 claims description 4
- 238000005507 spraying Methods 0.000 claims description 4
- 239000000839 emulsion Substances 0.000 claims description 3
- 238000004528 spin coating Methods 0.000 abstract description 18
- 239000011253 protective coating Substances 0.000 abstract description 9
- 238000009987 spinning Methods 0.000 abstract description 9
- 239000012260 resinous material Substances 0.000 abstract description 8
- 230000001681 protective effect Effects 0.000 abstract description 4
- 239000000796 flavoring agent Substances 0.000 abstract description 3
- 235000019634 flavors Nutrition 0.000 abstract description 3
- 239000000463 material Substances 0.000 description 10
- 239000000080 wetting agent Substances 0.000 description 7
- 239000000203 mixture Substances 0.000 description 6
- -1 polypropylene Polymers 0.000 description 6
- 239000004793 Polystyrene Substances 0.000 description 5
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 5
- 230000008901 benefit Effects 0.000 description 5
- 230000005540 biological transmission Effects 0.000 description 5
- 229920002223 polystyrene Polymers 0.000 description 5
- BQCIDUSAKPWEOX-UHFFFAOYSA-N 1,1-Difluoroethene Chemical compound FC(F)=C BQCIDUSAKPWEOX-UHFFFAOYSA-N 0.000 description 4
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 4
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 4
- 239000001301 oxygen Substances 0.000 description 4
- 229910052760 oxygen Inorganic materials 0.000 description 4
- 239000007789 gas Substances 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- 238000009736 wetting Methods 0.000 description 3
- GPOGMJLHWQHEGF-UHFFFAOYSA-N 2-chloroethyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCCl GPOGMJLHWQHEGF-UHFFFAOYSA-N 0.000 description 2
- ZGHFDIIVVIFNPS-UHFFFAOYSA-N 3-Methyl-3-buten-2-one Chemical compound CC(=C)C(C)=O ZGHFDIIVVIFNPS-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- 230000009286 beneficial effect Effects 0.000 description 2
- 230000001680 brushing effect Effects 0.000 description 2
- FUSUHKVFWTUUBE-UHFFFAOYSA-N buten-2-one Chemical compound CC(=O)C=C FUSUHKVFWTUUBE-UHFFFAOYSA-N 0.000 description 2
- 239000008199 coating composition Substances 0.000 description 2
- 230000001627 detrimental effect Effects 0.000 description 2
- FJKIXWOMBXYWOQ-UHFFFAOYSA-N ethenoxyethane Chemical compound CCOC=C FJKIXWOMBXYWOQ-UHFFFAOYSA-N 0.000 description 2
- 235000013305 food Nutrition 0.000 description 2
- 229920001903 high density polyethylene Polymers 0.000 description 2
- 239000004700 high-density polyethylene Substances 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 239000000123 paper Substances 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 239000000375 suspending agent Substances 0.000 description 2
- 239000012815 thermoplastic material Substances 0.000 description 2
- 239000002562 thickening agent Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- HERVEWIIWZKCRT-UHFFFAOYSA-N (4-cyclohexylphenyl) 2-methylprop-2-enoate Chemical compound C1=CC(OC(=O)C(=C)C)=CC=C1C1CCCCC1 HERVEWIIWZKCRT-UHFFFAOYSA-N 0.000 description 1
- KUIZKZHDMPERHR-UHFFFAOYSA-N 1-phenylprop-2-en-1-one Chemical compound C=CC(=O)C1=CC=CC=C1 KUIZKZHDMPERHR-UHFFFAOYSA-N 0.000 description 1
- IGGDKDTUCAWDAN-UHFFFAOYSA-N 1-vinylnaphthalene Chemical compound C1=CC=C2C(C=C)=CC=CC2=C1 IGGDKDTUCAWDAN-UHFFFAOYSA-N 0.000 description 1
- STMDPCBYJCIZOD-UHFFFAOYSA-N 2-(2,4-dinitroanilino)-4-methylpentanoic acid Chemical compound CC(C)CC(C(O)=O)NC1=CC=C([N+]([O-])=O)C=C1[N+]([O-])=O STMDPCBYJCIZOD-UHFFFAOYSA-N 0.000 description 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- GOXQRTZXKQZDDN-UHFFFAOYSA-N 2-Ethylhexyl acrylate Chemical class CCCCC(CC)COC(=O)C=C GOXQRTZXKQZDDN-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- IGDLZDCWMRPMGL-UHFFFAOYSA-N 2-ethenylisoindole-1,3-dione Chemical compound C1=CC=C2C(=O)N(C=C)C(=O)C2=C1 IGDLZDCWMRPMGL-UHFFFAOYSA-N 0.000 description 1
- KGIGUEBEKRSTEW-UHFFFAOYSA-N 2-vinylpyridine Chemical compound C=CC1=CC=CC=N1 KGIGUEBEKRSTEW-UHFFFAOYSA-N 0.000 description 1
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 1
- 239000004709 Chlorinated polyethylene Substances 0.000 description 1
- IEPRKVQEAMIZSS-UHFFFAOYSA-N Di-Et ester-Fumaric acid Natural products CCOC(=O)C=CC(=O)OCC IEPRKVQEAMIZSS-UHFFFAOYSA-N 0.000 description 1
- IEPRKVQEAMIZSS-WAYWQWQTSA-N Diethyl maleate Chemical compound CCOC(=O)\C=C/C(=O)OCC IEPRKVQEAMIZSS-WAYWQWQTSA-N 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 description 1
- HETCEOQFVDFGSY-UHFFFAOYSA-N Isopropenyl acetate Chemical compound CC(=C)OC(C)=O HETCEOQFVDFGSY-UHFFFAOYSA-N 0.000 description 1
- GYCMBHHDWRMZGG-UHFFFAOYSA-N Methylacrylonitrile Chemical compound CC(=C)C#N GYCMBHHDWRMZGG-UHFFFAOYSA-N 0.000 description 1
- 239000002033 PVDF binder Substances 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- XECAHXYUAAWDEL-UHFFFAOYSA-N acrylonitrile butadiene styrene Chemical compound C=CC=C.C=CC#N.C=CC1=CC=CC=C1 XECAHXYUAAWDEL-UHFFFAOYSA-N 0.000 description 1
- 229920000122 acrylonitrile butadiene styrene Polymers 0.000 description 1
- 239000004676 acrylonitrile butadiene styrene Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 235000013361 beverage Nutrition 0.000 description 1
- INLLPKCGLOXCIV-UHFFFAOYSA-N bromoethene Chemical compound BrC=C INLLPKCGLOXCIV-UHFFFAOYSA-N 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- UBAZGMLMVVQSCD-UHFFFAOYSA-N carbon dioxide;molecular oxygen Chemical compound O=O.O=C=O UBAZGMLMVVQSCD-UHFFFAOYSA-N 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000004581 coalescence Methods 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- OIWOHHBRDFKZNC-UHFFFAOYSA-N cyclohexyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OC1CCCCC1 OIWOHHBRDFKZNC-UHFFFAOYSA-N 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- OGVXYCDTRMDYOG-UHFFFAOYSA-N dibutyl 2-methylidenebutanedioate Chemical compound CCCCOC(=O)CC(=C)C(=O)OCCCC OGVXYCDTRMDYOG-UHFFFAOYSA-N 0.000 description 1
- ZEFVHSWKYCYFFL-UHFFFAOYSA-N diethyl 2-methylidenebutanedioate Chemical compound CCOC(=O)CC(=C)C(=O)OCC ZEFVHSWKYCYFFL-UHFFFAOYSA-N 0.000 description 1
- IEPRKVQEAMIZSS-AATRIKPKSA-N diethyl fumarate Chemical compound CCOC(=O)\C=C\C(=O)OCC IEPRKVQEAMIZSS-AATRIKPKSA-N 0.000 description 1
- ZWWQRMFIZFPUAA-UHFFFAOYSA-N dimethyl 2-methylidenebutanedioate Chemical compound COC(=O)CC(=C)C(=O)OC ZWWQRMFIZFPUAA-UHFFFAOYSA-N 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- XJELOQYISYPGDX-UHFFFAOYSA-N ethenyl 2-chloroacetate Chemical compound ClCC(=O)OC=C XJELOQYISYPGDX-UHFFFAOYSA-N 0.000 description 1
- UIWXSTHGICQLQT-UHFFFAOYSA-N ethenyl propanoate Chemical compound CCC(=O)OC=C UIWXSTHGICQLQT-UHFFFAOYSA-N 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 229920002313 fluoropolymer Polymers 0.000 description 1
- 239000012760 heat stabilizer Substances 0.000 description 1
- 229940090044 injection Drugs 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 238000001746 injection moulding Methods 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 239000004611 light stabiliser Substances 0.000 description 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- AWJZTPWDQYFQPQ-UHFFFAOYSA-N methyl 2-chloroprop-2-enoate Chemical compound COC(=O)C(Cl)=C AWJZTPWDQYFQPQ-UHFFFAOYSA-N 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- RAGRPVMAKIWULP-UHFFFAOYSA-N n'-ethenylbutanediamide Chemical compound NC(=O)CCC(=O)NC=C RAGRPVMAKIWULP-UHFFFAOYSA-N 0.000 description 1
- KKFHAJHLJHVUDM-UHFFFAOYSA-N n-vinylcarbazole Chemical compound C1=CC=C2N(C=C)C3=CC=CC=C3C2=C1 KKFHAJHLJHVUDM-UHFFFAOYSA-N 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 238000004806 packaging method and process Methods 0.000 description 1
- QIWKUEJZZCOPFV-UHFFFAOYSA-N phenyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OC1=CC=CC=C1 QIWKUEJZZCOPFV-UHFFFAOYSA-N 0.000 description 1
- 239000006223 plastic coating Substances 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 229920002981 polyvinylidene fluoride Polymers 0.000 description 1
- SCUZVMOVTVSBLE-UHFFFAOYSA-N prop-2-enenitrile;styrene Chemical compound C=CC#N.C=CC1=CC=CC=C1 SCUZVMOVTVSBLE-UHFFFAOYSA-N 0.000 description 1
- 239000001044 red dye Substances 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 229920006298 saran Polymers 0.000 description 1
- 235000015096 spirit Nutrition 0.000 description 1
- 229920000638 styrene acrylonitrile Polymers 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
- 238000007666 vacuum forming Methods 0.000 description 1
- 229910001868 water Inorganic materials 0.000 description 1
Images
Classifications
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B05—SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D—PROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D7/00—Processes, other than flocking, specially adapted for applying liquids or other fluent materials to particular surfaces or for applying particular liquids or other fluent materials
- B05D7/22—Processes, other than flocking, specially adapted for applying liquids or other fluent materials to particular surfaces or for applying particular liquids or other fluent materials to internal surfaces, e.g. of tubes
- B05D7/227—Processes, other than flocking, specially adapted for applying liquids or other fluent materials to particular surfaces or for applying particular liquids or other fluent materials to internal surfaces, e.g. of tubes of containers, cans or the like
-
- 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
- B29C49/00—Blow-moulding, i.e. blowing a preform or parison to a desired shape within a mould; Apparatus therefor
- B29C49/22—Blow-moulding, i.e. blowing a preform or parison to a desired shape within a mould; Apparatus therefor using multilayered preforms or parisons
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B05—SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D—PROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D1/00—Processes for applying liquids or other fluent materials
- B05D1/002—Processes for applying liquids or other fluent materials the substrate being rotated
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B05—SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D—PROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D2201/00—Polymeric substrate or laminate
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B05—SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D—PROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D3/00—Pretreatment of surfaces to which liquids or other fluent materials are to be applied; After-treatment of applied coatings, e.g. intermediate treating of an applied coating preparatory to subsequent applications of liquids or other fluent materials
- B05D3/02—Pretreatment of surfaces to which liquids or other fluent materials are to be applied; After-treatment of applied coatings, e.g. intermediate treating of an applied coating preparatory to subsequent applications of liquids or other fluent materials by baking
- B05D3/0254—After-treatment
- B05D3/0263—After-treatment with IR heaters
-
- 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
- B29C2949/00—Indexing scheme relating to blow-moulding
- B29C2949/20—Preforms or parisons whereby a specific part is made of only one component, e.g. only one layer
- B29C2949/22—Preforms or parisons whereby a specific part is made of only one component, e.g. only one layer at neck portion
-
- 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
- B29C2949/00—Indexing scheme relating to blow-moulding
- B29C2949/20—Preforms or parisons whereby a specific part is made of only one component, e.g. only one layer
- B29C2949/24—Preforms or parisons whereby a specific part is made of only one component, e.g. only one layer at flange portion
-
- 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
- B29C2949/00—Indexing scheme relating to blow-moulding
- B29C2949/20—Preforms or parisons whereby a specific part is made of only one component, e.g. only one layer
- B29C2949/26—Preforms or parisons whereby a specific part is made of only one component, e.g. only one layer at body portion
-
- 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
- B29C2949/00—Indexing scheme relating to blow-moulding
- B29C2949/20—Preforms or parisons whereby a specific part is made of only one component, e.g. only one layer
- B29C2949/28—Preforms or parisons whereby a specific part is made of only one component, e.g. only one layer at bottom portion
-
- 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
- B29C2949/00—Indexing scheme relating to blow-moulding
- B29C2949/30—Preforms or parisons made of several components
- B29C2949/3008—Preforms or parisons made of several components at neck portion
-
- 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
- B29C2949/00—Indexing scheme relating to blow-moulding
- B29C2949/30—Preforms or parisons made of several components
- B29C2949/3012—Preforms or parisons made of several components at flange portion
-
- 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
- B29C2949/00—Indexing scheme relating to blow-moulding
- B29C2949/30—Preforms or parisons made of several components
- B29C2949/3016—Preforms or parisons made of several components at body portion
-
- 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
- B29C2949/00—Indexing scheme relating to blow-moulding
- B29C2949/30—Preforms or parisons made of several components
- B29C2949/302—Preforms or parisons made of several components at bottom portion
-
- 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
- B29C2949/00—Indexing scheme relating to blow-moulding
- B29C2949/30—Preforms or parisons made of several components
- B29C2949/3024—Preforms or parisons made of several components characterised by the number of components or by the manufacturing technique
-
- 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
- B29C2949/00—Indexing scheme relating to blow-moulding
- B29C2949/30—Preforms or parisons made of several components
- B29C2949/3024—Preforms or parisons made of several components characterised by the number of components or by the manufacturing technique
- B29C2949/3026—Preforms or parisons made of several components characterised by the number of components or by the manufacturing technique having two or more components
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/26—Web or sheet containing structurally defined element or component, the element or component having a specified physical dimension
- Y10T428/263—Coating layer not in excess of 5 mils thick or equivalent
- Y10T428/264—Up to 3 mils
- Y10T428/265—1 mil or less
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31511—Of epoxy ether
Definitions
- ABSTRACT A method for spin coating the interior of a generally rigid or semi-rigid plastic hollow article, such as a container or parison, with a synthetic organic resinous material to provide a protective coating therein.
- the method comprises placing a quantity of a dispersion of synthetic organic resinous material, preferably a latex or solution, in a hollow article, spinning the article at high speed thereby causing centrifugal force to distribute and hold a coating of the dispersion uniformly on the interior surfaces of the same and then heating the coating while continuing to spin the article.
- the result of the spin coating method is an article with a substantially uniform interior protective film providing improved article characteristics such as gas and liquid barrier properties, color and appearance, taste and flavor protection and the like.
- One of the primary problems associated with the prior art coating methods is their inability to form uniform coatings without coating sag substantially in excess of 0.1 mil in thickness on the walls of a container without the addition of thickeners which are detrimental to the properties of the resulting film.
- Another problem is their inability, when used to coat a latex, to completely wet-out and maintain a wetted surface of a nonporous substrate such as a plastic without the addition of substantial amounts of wetting agents which are also detrimental to the properties of the resulting film.
- the present invention provides a method for uniformly spin coating the interior walls of generally rigid or semi-rigid plastic hollow articles such as a container or parison, for forming the same, with a synthetic organic resinous material, hereinafter commonly referred to as plastic material, which will result in an article having an interior protective coating providing improved characteristics.
- the method comprises placing, preferably spraying or brushing, a quantity of a dispersion of plastic material in a hollow article, spinning the same at a high speed thereby causing centrifugal force to distribute and/or hold a coating of the dispersion uniformly on the interior wall surfaces of the article and then heating the coating to dry or fuse the same while continuing to spin the article.
- the dispersion of synthetic organic resinous material may be a latex, emulsion, suspension, solution or the like but is preferably a latex or suspension.
- the article is spun at a high rate of speed of at least 100 r.p.m., preferably from about 1,000 to 5,000 r.p.m., with the resulting centrifugal force distributing and/or holding the dispersion uniformly on the walls of the article.
- the coating may be dried or fused by inserting an infrared or other like heating element into the article, blowing hot air into.
- dielectric heating, microwave heating or other known heating means or combinations thereof while continuing to spin the same with the coating being held to the container walls by the centrifugal force.
- the drying time of the coating is dependent on thickness of coating, amount and type of heating and the like. Application of multiple layers of coating, including adhesive or tie coatings applied before the protective coatings, fall within the scope of the invention.
- the plastic dispersion is preferably a latex or suspension of saran, polyvinyl chloride, polyamide, olefins, acrylonitrile, epoxy or other like plastic resins or copolymers or blends thereof which will form the desired protective coating in the parison or container.
- the hollow articles may be thermoformed by extrusion, injec tion molding, vacuum forming, blow molding and the like from polymers such as polystyrene, polypropylene, polyethylene, acrylonitrile butadiene styrene, styrene acrylonitrile, vinyl chloride, arylonitrile or like high structural strength polymers or copolymers or blends thereof which will not, in most cases, meet the necessary requirements for the products contained therein.
- the polymers in the article walls may be multiaxially molecular oriented or unoriented depending on desired end product. A more detailed description of various useful polymers will be discussed later.
- the method described herein is directed towards, but not limited to, the fabrication of a pressurized or nonpressurized container for packaging food products, oil and greases, beverages, medicine and the like where the protective coating helps provide improved container characteristics such as a barrier to oxygen, carbon dioxide, nitrogen, water or water vapor and organic vapor or liquid transmission into or out of the container.
- improved container characteristics such as color and appearance, taste and flavor protection, stress crack and chemical resistance and the like may also be achieved.
- the method herein described provides many advantages over more conventional prior art coating methods such as a symmetrically uniform coating thickness without coating sag, improved adhesion of the coating to the container or parison wall substrate due to forced wetting, reduced need for wetting agents, thickeners or other additives in the coating formulation, a more continuous layer of coating with substantially fewer pinholes therein due to a high degree of coalescence of the wet coating during spinning of the container or parison and a reduced drying time of the coating as, for example, where the polymer in a latex or suspension is of higher density than the suspending agents, such as a saran latex, the polymer is forced to the container or parison wall leaving the suspending agent at the heated surface during spinning of the container where it can be more easily removed by drying.
- the parisons coated by the method herein described may be used to form containers having an interior protective coating.
- coated containers can be formed from coated parisons by conventional blow molding.
- an additional advantage is obtained by combining the spin coating method with a blow molding operation to form an internally coated container.
- the heat used to dry the coating can be also used to soften the inside parison walls prior to the actual blowing of the container.
- the interior heat in the spin coated parison need only be retained while additional external heat is applied to soften the parison before the container blowing step. By using this sequence of steps, the time required to heat parisons for blow molding can be substantially reduced.
- a still further object of the present invention is to provide a combined method for spin coating the interior of parisons with protective coatings and then blow molding said coated parisons into coated containers utilizing the heat for drying or fusing the coatings in the parisons to help soften the parisons for subsequent blowing of the containers.
- FIG. 1 is an exaggerated cross-sectional view of a cup shaped container for food products and the like constructed according to the principles of the present invention
- FIG. 2 is a side elevation view, with portions broken away, of a parison which may be used to make a container and which is constructed according to the principles of the present invention
- FIG. 3 is a view like FIG. 1 only showing a modified bottle shaped container
- FIG. 4 is a schematic representation of the sequence of steps followed in accordance with the principles of the present invention showing spin coating of a container similar to that shown in FIG. 1;
- FIG. 5 is a schematic representation of the sequence of steps followed in accordance with the principles of the present invention showing spin coating of a parison similar to that shown in FIG. 2 and then blow molding of the same into an internally coated container utilizing the heat for drying or fusing the coating to help soften the parison prior to blowing the container.
- FIG. 1 illustrates a plastic cup-shaped container 10 having a side wall 12 and a bottom wall 14.
- Container 10 is formed from a high structural strength thermoplastic material 16.
- a plastic coating 18 is bonded to interior of walls 12 and 14.
- FIG. 2 illustrates a parison 20 used to blow mold a container, similar to that shown in FIG. 3, having a thermoplastic wall 22 to which a coating 24, similar to coating 18 shown in FIG. 1, is bonded.
- FIG. 3 illustrates a bottle shaped container 30 having a side wall 32, a bottom wall 34 and a neck portion 36 which is formed from a thermoplastic material 38.
- a coating 39 similar to coating 18 shown in FIG. 1, is bonded to the interior of walls 32 and 34 and the neck portion 36.
- step 1 illustrates the selection of a container, similar to that shown in FIG. 1, which is then spun and sprayed on the interior walls with a synthetic organic resinous dispersion, as shown in step 2.
- step 3 of FIG. 4 illustrates the drying or fusion of the distributed coating while being held to the container walls by the centrifugal force with an infrared heating element which is inserted into the container while continuing to spin the same.
- Step 4 illustrates the resulting container with an internal protective coating adhered to the walls of the container.
- Steps 1 and 2 of FIG. 5 illustrate the selection and spin coating of a parison, similar to that shown in FIG. 2, following the same procedure represented by FIG. 4.
- step 3 the parison is held by a heated mandrel to retain the drying or fusion heat within the parison and is externally heated in an oven utilizing any known heating means.
- Step 4 of FIG. 5 illustrates the subsequent blow molding of the internally coated parison and step 5 illustrates the resulting internally coated blown container which is similar to the container shown in FIG. 3.
- Example 1 To illustrate the method herein described, a plastic cup-shaped container, like container 10 shown in FIG. 1, having a wall thickness of about 50 mils, a diameter of about 3% inches and a height of about 4 inches formed of a general purpose polystyrene material was selected.
- a variable speed motor fitted with a spindle wihch holds the container was used to spin the container.
- the container was placed in the spindle and 3 grams of a saran latex poured into the same.
- the container was then spun for 10 seconds at about 5,000 rpm. with the excess latex allowed to flow out the mouth of the container.
- a 600 watt infrared heating element was inserted into the container for 10 seconds to dry the latex.
- the dried coating thickness was a uniform 0.4 mils on the side wall and 0.1 mils on the bottom wall.
- the saran latex used in this example was formulated with about 57 weight percent solids and 2 weight percent wetting agent.
- the saran component comprises about weight percent of a copolymer of vinylidene chloride with the balance being acrylonitrile and methyl methacrylate copolymers.
- the wetting agent is of the type generally referred to as an alkylphenoxypoly(oxyethylene)ethanol having the general formula RC I-I O(CH CI-I O),,CH CH OH in which R may be C I-I or a higher homolog.
- the coating on the container side wall demonstrates very good adhesion and could be removed with a 9% inch wide strip of No. 810 Scotch tape only after three attempts in the same area of the wall.
- the dried film exhibited complete wet-out on the container walls.
- a flat sheet of a similar general purpose polystyrene material was coated with the same saran latex using a wire wound rod and then dried for seconds with a 600 watt infrared heating element.
- the dried film exhibited incomplete wetting out on the flat sheet.
- a 0.4 mil thick portion of the coating was easily removed with tape from the sheet with only one attempt. The difference in adhesion and wet-out were attributed to the forced wetting of the walls of the containerwhen the spin coating method herein described was used.
- Example 2 To demonstrate the uniformity and lack of coating sag achieved by the spin coating method, a cup-shaped container similar to that described in Example 1 was spin coated at 1,800 r.p.m. The same saran latex and spinning and drying times were used. The resulting dried coating on the interior side wall of the container was a uniform 0.4 mil thick. Asecond container was spin coated following the same procedure except that the spinning step was discontinued before the coating was dried with the infrared heating element. The resulting dried coating on the side wall of the container exhibited severe coating sag and nonuniformity.
- Example 3 To demonstrate the improved barrier properties of a container coated with the method herein described, a cup-shaped container, like container 10 in FIG.
- Example 1 having a wall thickness of about 40 mils, a diameter of about 3% inches and a height of about 3% inches formed of a high density polyethylene material was selected. The same procedures and equipment used in Example 1 are employed here. Three grams of a saran latex was placed in the container, the container was spun at about 5,000 rpm. for 10 seconds and then dried for seconds while continuing to spin the container.
- the high density polyethylene forming the container walls was polymerized by Ziegler catalysts and had a density of about 0.959, a melt index of about 0.5 and a flexual modulus of about 170,000.
- the saran latex used here was the same as that used in Example 1 except it was formulated with about 4 weight percent wetting agent.
- the resulting dried coating was a uniform 0.3 mil thick on the side wall of the container.
- the average oxygen transmission rate determined by mass spectrometer analysis of two samples taken from the side wall of the container was found to be 0.63 cubic centimeter per 100 square inches per day at atmospheric pressure and 23C.
- the average oxygen transmission rate, tested in the same manner, of four 40 mil thick samples taken from the side wall of a similar uncoated container was found to be 2.78 cubic centimeters per 100 square inches per day at atmospheric pressure and 23C.
- Example 4 To illustrate the method of spin coating and blow molding of a parison, like the parison with a tapered side wall shown in FIG. 5, into an internally coated container, like container 30 of FIG.
- Example 3 an injection molded, closed end, multiaxially oriented, general purpose polystyrene parison was selected which had a wall thickness of about 40 mils, a base diameter of 1% inches and an upper diameter just below the neck of 1% inches and an overall height of 4% inches. The same procedures and equipment used in Example 1 are employed here. Two grams of a saran latex was poured into the parison,
- the parison was spun for 2 seconds at 5,000 rpm. and then a 500 watt infrared heating element was inserted into the parison for 4 seconds to dry the latex while continuing to spin the parison.
- a second coating of the latex was applied over the first coating using the same conditions and procedures as described above. The dried coating had an evenly distributed thickness of 0.4 mil at the bottom and 0.6 mil at the top of the parison with the average being 0.5 mil.
- the saran latex used in this example was formulated with about weight percent solids and 2 weight percent wetting agent.
- the saran component comprised about 92 weight percent of a copolymer of vinylidene chloride with the balance being an acrylonitrile copolymer.
- the wetting agent was the same general type employed in Example 1.
- the coated parison was then blow molded using conventional equipment. To heat soften the parison, it was placed on a mandrel, similar to that shown in FIG. 5, which had a surface, temperature of 220F. External heating was accomplished by placing the parison and mandrel for 14 seconds in an oven heated by radiant heating elements having a surface temperature of l,000F. The parison was then placed in a mold and blown into a container, like container 30 shown in FIG. 3, with an air pressure of psi. for a period of 5 seconds. The dwell time of the container in the mold was 3 seconds.
- the blow molded container had an average side wall thickness of about 10 mils, a body diameter of 3 3/16 inches, a neck diameter of 1 /8 inches and height of 4% inches.
- the coating on the side wall of the container was reduced in thickness proportionally with the reduction in thickness of the side wall substrate and had an average thickness of about 0.125 mils.
- the blown container showed that it exhibited the characteristic increased toughness of a multiaxially molecular oriented container. Also, the coating had sufficient adhesion to the container wall substrate to flow therewith without any detachment when the container was blown.
- the coating in the blown container was continuous and pinhole free as determined by placing a mineral spirits and red dye solution into coated and uncoated blown containers for a period of one-half hour. The uncoated general purpose polystyrene containers were stained red whereas the coated containers remained unchanged.
- the average oxygen transmission rate detennined by mass spectrometer analysis of three samples taken from the side wall of the coated containers was found to be 0.93 cubic centimeter per hundred square inches per day at atmospheric pressure and 23C.
- the average oxygen transmission rate, tested in the same manner, of three samples taken from the side walls of similar uncoated containers is found to be 23.0 cubic centimeters per hundred square inches per day at atmospheric pressure and 23C.
- Particularly suited polymers are vinylidene chloride, vinyl chloride, acrylonitrile, vinylidene fluoride and/or combined mixtures thereof.
- Particular advantageous and beneficial are compositions of vinylidene chloride polymers, wherein the polymers contain at least about weight percent vinylidene chloride, the remainder being one or more olefinically unsaturated monomers copolymerizable therewith.
- Suitable vinylidene chloride polymers are prepared utilizing such comonomers as methyl, ethyl, isobutyl, butyl, octyl and 2-ethylhexyl acrylates and methacrylate; phenyl methacrylate, cyclohexyl methacrylate, pcyclohexylphenyl methacrylate, chloroethyl methacrylate, p-cyclohexylphenyl methacrylate, chloroethyl methacrylate, 2-nitro-2-methylpropyl methaerylate, and the corresponding esters of acrylic acid, methyl alphachloro-acrylate, octyl alphachloroacrylate, methyl isopropenyl ketone, acrylonitrile, methacrylonitrile, methyl vinyl ketone, vinyl chloride, vinyl acetate, vinyl propionate, vinyl chloroacetate, vinyl bromide, styrene,
- compositions which may be used with benefit in coatings in accordance with the present invention are vinyl chloride polymers which contain a predominant amount of vinyl chloride therein. Fluorocarbon polymers, fluorohydrocarbon polymers and fluorohalohydrocarbon polymers may also be used with benefit.
- a method for internally coating a generally rigid or semi-rigid plastic container or parison type hollow article comprising:
- said dispersion comprises a latex the major resin component of which is a copolymer having copolymerized therein at least about weight percent vinylidene chloride and a remainder of one or more copolymerizable olefinically unsaturated monomers.
- said dispersion comprises a suspension the major resin component of which is a copolymer having copolymerized therein at least 70 weight percent vinylidene chloride and a remainder of one or more copolymerizable oleflnically unsaturated monomers.
- said dispersion comprises an emulsion the major resin component of which is epoxy resin.
- said dispersion comprises a suspension the major resin component of which is epoxy resin.
- said dispersion comprises a latex the major resin component of which is acrylonitrile polymer.
- said dispersion comprises a suspension the major resin component of which is acrylonitrile polymer.
Landscapes
- Engineering & Computer Science (AREA)
- Manufacturing & Machinery (AREA)
- Mechanical Engineering (AREA)
- Life Sciences & Earth Sciences (AREA)
- Wood Science & Technology (AREA)
- Coating Of Shaped Articles Made Of Macromolecular Substances (AREA)
- Blow-Moulding Or Thermoforming Of Plastics Or The Like (AREA)
- Laminated Bodies (AREA)
- Details Of Rigid Or Semi-Rigid Containers (AREA)
Priority Applications (11)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US00147120A US3804663A (en) | 1971-05-26 | 1971-05-26 | Method of internally coating rigid or semi-rigid plastic containers |
| CA140,992,A CA950281A (en) | 1971-05-26 | 1972-05-01 | Method of internally coating rigid or semi-rigid plastic containers |
| AU41981/72A AU465035B2 (en) | 1971-05-26 | 1972-05-05 | Method of internally coating rigid or semirigid plastic containers |
| NL7206817A NL7206817A (OSRAM) | 1971-05-26 | 1972-05-19 | |
| IT50434/72A IT958018B (it) | 1971-05-26 | 1972-05-23 | Procedimento per il rivestimento interno di contenitori di plasti ca rigidi o semi rigidi e prodot to ottenuto |
| DE19722225040 DE2225040A1 (de) | 1971-05-26 | 1972-05-23 | Verfahren zum Beschichten der Innenwände von steifen oder halbsteifen Kunststoffbehältern |
| GB2477072A GB1389572A (en) | 1971-05-26 | 1972-05-25 | Method of internally coating rigid or semirigid plastics hollow articles |
| FR7218667A FR2139027B1 (OSRAM) | 1971-05-26 | 1972-05-25 | |
| SE7206818A SE374317B (OSRAM) | 1971-05-26 | 1972-05-25 | |
| BR003328/72A BR7203328D0 (pt) | 1971-05-26 | 1972-05-25 | Processo para revestimento interno de um artigo plastico oco rigido ou semi-rigido |
| BE783932A BE783932A (fr) | 1971-05-26 | 1972-05-25 | Procede de revetement de la surface interne de recipients de matieres plastiques rigides ou semi-rigides |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US00147120A US3804663A (en) | 1971-05-26 | 1971-05-26 | Method of internally coating rigid or semi-rigid plastic containers |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US3804663A true US3804663A (en) | 1974-04-16 |
Family
ID=22520360
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US00147120A Expired - Lifetime US3804663A (en) | 1971-05-26 | 1971-05-26 | Method of internally coating rigid or semi-rigid plastic containers |
Country Status (11)
| Country | Link |
|---|---|
| US (1) | US3804663A (OSRAM) |
| AU (1) | AU465035B2 (OSRAM) |
| BE (1) | BE783932A (OSRAM) |
| BR (1) | BR7203328D0 (OSRAM) |
| CA (1) | CA950281A (OSRAM) |
| DE (1) | DE2225040A1 (OSRAM) |
| FR (1) | FR2139027B1 (OSRAM) |
| GB (1) | GB1389572A (OSRAM) |
| IT (1) | IT958018B (OSRAM) |
| NL (1) | NL7206817A (OSRAM) |
| SE (1) | SE374317B (OSRAM) |
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| JPS5951889B2 (ja) * | 1979-08-31 | 1984-12-17 | 固 青木 | 射出延伸吹込成形法 |
| AU6093480A (en) * | 1979-10-04 | 1981-04-09 | Schenectady Chemicals Inc. | Microwave curing of resins |
| DE3314108A1 (de) * | 1983-04-19 | 1984-10-25 | C.F. Spiess & Sohn Kunststoffwerk GmbH & Co, 6719 Kleinkarlbach | Verfahren und vorrichtung zum herstellen von hohlkoerpern mit zumindest bereichsweise zwei- oder mehrschichtiger wand |
| GB8925472D0 (en) * | 1989-11-10 | 1989-12-28 | Ici Plc | Container |
| MX2021012817A (es) * | 2019-04-19 | 2022-03-04 | Photex Inc | Sistema y metodo para curar el interior de la lata. |
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- 1972-05-05 AU AU41981/72A patent/AU465035B2/en not_active Expired
- 1972-05-19 NL NL7206817A patent/NL7206817A/xx unknown
- 1972-05-23 DE DE19722225040 patent/DE2225040A1/de active Pending
- 1972-05-23 IT IT50434/72A patent/IT958018B/it active
- 1972-05-25 FR FR7218667A patent/FR2139027B1/fr not_active Expired
- 1972-05-25 BE BE783932A patent/BE783932A/xx unknown
- 1972-05-25 GB GB2477072A patent/GB1389572A/en not_active Expired
- 1972-05-25 SE SE7206818A patent/SE374317B/xx unknown
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| US4025664A (en) * | 1974-01-02 | 1977-05-24 | Eppco | Container coating method |
| US4169906A (en) * | 1975-09-15 | 1979-10-02 | Rexnord Inc. | Wear resistant coated pipe and method of making it |
| US4093350A (en) * | 1976-05-19 | 1978-06-06 | Xerox Corporation | System for centrifugally casting a thin film plastic in a replica process for providing multi-faceted polygonal scanners |
| US4427122A (en) | 1977-05-13 | 1984-01-24 | Platmanufaktur A.B. | Container for liquids, which are sensitive to light |
| US4515832A (en) * | 1977-06-24 | 1985-05-07 | Rexnord, Inc. | Method for coating the inside of pipe |
| US4262627A (en) * | 1977-06-24 | 1981-04-21 | Rexnord, Inc. | Apparatus for coating the inside of pipe |
| US4370368A (en) * | 1980-05-07 | 1983-01-25 | Toyo Seikan Kaisha, Ltd. | Plastic bottles and process for preparation thereof |
| US4486378A (en) * | 1980-05-07 | 1984-12-04 | Toyo Seikan Kaisha Ltd. | Plastic bottles and process for preparation thereof |
| US4311250A (en) * | 1980-05-12 | 1982-01-19 | The Continental Group, Inc. | Container having internal wall surfaces modified to reduce carbonation loss |
| US4393106A (en) * | 1980-10-31 | 1983-07-12 | Toyo Seikan Kaisha Ltd. | Laminated plastic container and process for preparation thereof |
| US4427470A (en) | 1981-09-01 | 1984-01-24 | University Of Utah | Vacuum molding technique for manufacturing a ventricular assist device |
| US4699809A (en) * | 1981-11-05 | 1987-10-13 | Toyo Seikan Kaisha, Ltd. | Process for preparation of coated oriented plastic container |
| US4473423A (en) | 1982-05-03 | 1984-09-25 | University Of Utah | Artificial heart valve made by vacuum forming technique |
| US4714580A (en) * | 1982-05-28 | 1987-12-22 | Toyo Seikan Kaisha, Ltd. | Plastic vessel having oriented coating and process for preparation thereof |
| US4515836A (en) * | 1982-07-16 | 1985-05-07 | Nordson Corporation | Process for coating substrates with aqueous polymer dispersions |
| EP0099727A3 (en) * | 1982-07-16 | 1985-10-16 | Nordson Corporation | Method and apparatus for the polymer coating of substrates |
| US4687677A (en) * | 1983-04-06 | 1987-08-18 | V-J System Ab | Method and a device for lining pipelines by means of a flexible hose containing a curable plastic |
| US4650699A (en) * | 1983-04-18 | 1987-03-17 | Sermetel | Thixotropic alumina coating compositions, parts and methods |
| US4581259A (en) * | 1983-08-24 | 1986-04-08 | Rambaud Jean Michel | Composition and method for coating objects of acrylic resin and coated objects thus obtained |
| US4581247A (en) * | 1984-01-05 | 1986-04-08 | Insituform International N.V. | Lining of pipelines and passageways |
| US4554347A (en) * | 1984-07-20 | 1985-11-19 | W. R. Grace & Co. | Microwave curing of latex-based compositions |
| US4675139A (en) * | 1985-10-21 | 1987-06-23 | Continental Can Company, Inc. | Method of forming plastisol gaskets in container closures fabricated from synthetic plastic resins |
| US4851337A (en) * | 1986-01-08 | 1989-07-25 | Hygeia Sciences, Inc. | Extraction of test substances |
| US4846359A (en) * | 1987-12-18 | 1989-07-11 | The Procter & Gamble Company | Multi-layered plastic bottle having integrally formed handle and method of making |
| US5976450A (en) * | 1990-09-13 | 1999-11-02 | Mreijen; Hubertus | Preform for polyester bottle |
| US5766489A (en) * | 1993-09-13 | 1998-06-16 | Pts Gesellschaft Fuer Physikalisch-Technische Studien Jena Mbh | Process and arrangement for continously carrying out photoreactions in a liquid phase |
| US5906787A (en) * | 1994-02-18 | 1999-05-25 | The Coca-Cola Company | Hollow containers having a very thin inert or impermeable inner surface layer by coating the inside surface of the preform |
| US6444155B1 (en) | 1994-02-18 | 2002-09-03 | The Coca-Cola Company | Hollow containers having a very thin inert or impermeable inner surface layer by coating the inside surface of the preform |
| US5500308A (en) * | 1994-05-02 | 1996-03-19 | Rayovac Corporation | Electrochemical cell having an inner seal member |
| US5849224A (en) * | 1995-06-26 | 1998-12-15 | The Elizabeth And Sandor Valyi Foundation, Inc. | Process of blow molding a food and beverage container with a melt phase polyester layer |
| US6077578A (en) * | 1995-06-26 | 2000-06-20 | The Elizabeth And Sandor Valyi Foundation, Inc. | Molded plastic food and beverage container and method |
| US5632406A (en) * | 1995-10-11 | 1997-05-27 | Robbins, Iii; Edward S. | Side wall construction for collapsible containers |
| US5860556A (en) * | 1996-04-10 | 1999-01-19 | Robbins, Iii; Edward S. | Collapsible storage container |
| US6051295A (en) * | 1996-05-16 | 2000-04-18 | The Coca-Cola Company | Method for injection molding a multi-layer preform for use in blow molding a plastic bottle |
| US5965081A (en) * | 1996-05-16 | 1999-10-12 | The Coca-Cola Company | Method of making side-gated preforms for use in blow molding plastic bottles |
| US5851471A (en) * | 1996-05-16 | 1998-12-22 | The Coca-Cola Company | Method for injection molding a multi-layer preform for use in blow molding a plastic bottle |
| US5707691A (en) * | 1996-08-27 | 1998-01-13 | The Coca-Cola Company | Coating hollow containers by in-situ polymerization of monomers in bi-axially orientated form |
| US6520719B1 (en) | 1997-11-26 | 2003-02-18 | Insituform (Netherlands) B.V. | Apparatus for installing a flexible cured in place lateral seal in an existing main pipeline |
| US6068725A (en) * | 1997-11-26 | 2000-05-30 | Insituform (Netherlands) B.V. | Method of installation of a flexible cured in place lateral seal in an existing main pipeline |
| US6029726A (en) * | 1997-11-26 | 2000-02-29 | Insituform (Netherlands) B.V. | Apparatus for installing a flexible cured in place lateral seal in an existing main pipeline |
| US6044867A (en) * | 1997-11-26 | 2000-04-04 | Insituform (Netherlands) N.V. | Method and apparatus for fabricating a flexible lining with flexible collar for lining lateral pipelines |
| US5915419A (en) * | 1997-11-26 | 1999-06-29 | Insituform (Netherlands) B.V. | Cured in place lateral seal for relining of pipelines and method of manufacture |
| US6709698B1 (en) * | 1998-07-03 | 2004-03-23 | L'oreal | Method and apparatus for applying a coating such as a paint or a varnish |
| EP0968770A1 (fr) * | 1998-07-03 | 2000-01-05 | L'oreal | Procédé et dispositif pour appliquer un revêtement tel qu'une peinture ou un vernis |
| US6393803B1 (en) | 1998-11-06 | 2002-05-28 | Graham Packaging Company, L.P. | Process for coating blow-molded plastic containers |
| US6331331B1 (en) | 1999-04-29 | 2001-12-18 | Colgate-Palmolive Company | Decorated polyester tube package for aqueous compositions |
| US20030007891A1 (en) * | 1999-08-20 | 2003-01-09 | Wilson Robert F. | Apparatus and method of detecting fluid |
| US6545594B1 (en) | 2000-05-25 | 2003-04-08 | The Coca-Cola Company | Audio closure |
| EP1175918A3 (de) * | 2000-07-28 | 2002-04-10 | Schott Glas | Verfahren und Vorrichtung zum Auftragen einer hitzefixierten Gleitmittelschicht |
| US6586039B2 (en) * | 2000-07-28 | 2003-07-01 | Schott Glas | Process and apparatus for applying a thermally attached lubricating coating on an interior wall of a cylindrical container for medicinal purposes |
| US20020012741A1 (en) * | 2000-07-28 | 2002-01-31 | Jochen Heinz | Process and apparatus for applying a thermally attached lubricating coating on an interior wall of a cylindrical container for medicinal purposes |
| US7871558B2 (en) | 2002-06-20 | 2011-01-18 | Alcan Global Pharmaceutical Packaging, Inc. | Containers intended for moisture-sensitive products |
| US8003179B2 (en) | 2002-06-20 | 2011-08-23 | Alcan Packaging Flexible France | Films having a desiccant material incorporated therein and methods of use and manufacture |
| WO2005062825A3 (en) * | 2003-12-22 | 2006-09-21 | Nova Chem Inc | Disposable containers coated with a latex coating |
| RU2312873C1 (ru) * | 2003-12-22 | 2007-12-20 | Нова Кемикалз Инк. | Одноразовый контейнер с латексным покрытием |
| US20070080163A1 (en) * | 2005-10-12 | 2007-04-12 | Sar Holdings International Ltd. | Flexible mould for food baking |
| US8110260B2 (en) | 2007-02-02 | 2012-02-07 | Rick Merical | Containers intended for moisture-sensitive products |
| US20110020576A1 (en) * | 2009-07-24 | 2011-01-27 | Fina Technology, Inc. | Polystyrene Preform Design for Blow Molding of Articles |
| US20140203019A1 (en) * | 2010-10-19 | 2014-07-24 | Superfos A/S | Container comprising an inner lining, a method of applying such a lining to a container and use of a peel-able coating as an inner lining in a container |
| US9604252B2 (en) | 2013-05-20 | 2017-03-28 | Conopco, Inc. | Process for coating containers |
| US12280396B2 (en) | 2019-04-19 | 2025-04-22 | Photex Inc. | Narrowband can manufacturing |
Also Published As
| Publication number | Publication date |
|---|---|
| IT958018B (it) | 1973-10-20 |
| DE2225040A1 (de) | 1972-12-07 |
| SE374317B (OSRAM) | 1975-03-03 |
| AU465035B2 (en) | 1975-09-18 |
| FR2139027A1 (OSRAM) | 1973-01-05 |
| NL7206817A (OSRAM) | 1972-11-28 |
| BE783932A (fr) | 1972-11-27 |
| FR2139027B1 (OSRAM) | 1976-01-16 |
| BR7203328D0 (pt) | 1973-05-10 |
| CA950281A (en) | 1974-07-02 |
| AU4198172A (en) | 1973-11-08 |
| GB1389572A (en) | 1975-04-03 |
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