USRE36815E - Flavor protectant closure liner compositions - Google Patents
Flavor protectant closure liner compositions Download PDFInfo
- Publication number
- USRE36815E USRE36815E US09/398,935 US39893599A USRE36815E US RE36815 E USRE36815 E US RE36815E US 39893599 A US39893599 A US 39893599A US RE36815 E USRE36815 E US RE36815E
- Authority
- US
- United States
- Prior art keywords
- compound
- liner
- flavor
- liner composition
- hydrazide
- 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 - Fee Related
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 136
- 239000000796 flavoring agent Substances 0.000 title claims abstract description 103
- 235000019634 flavors Nutrition 0.000 title claims description 61
- -1 tocopherol compound Chemical class 0.000 claims abstract description 44
- GVJHHUAWPYXKBD-UHFFFAOYSA-N d-alpha-tocopherol Natural products OC1=C(C)C(C)=C2OC(CCCC(C)CCCC(C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-UHFFFAOYSA-N 0.000 claims abstract description 42
- 239000012530 fluid Substances 0.000 claims abstract description 40
- 239000000126 substance Substances 0.000 claims abstract description 24
- 238000000034 method Methods 0.000 claims abstract description 22
- 235000019640 taste Nutrition 0.000 claims abstract description 22
- 239000011732 tocopherol Substances 0.000 claims abstract description 18
- 229930003799 tocopherol Natural products 0.000 claims abstract description 18
- 235000010384 tocopherol Nutrition 0.000 claims abstract description 17
- 229960001295 tocopherol Drugs 0.000 claims abstract description 17
- 150000001875 compounds Chemical class 0.000 claims description 62
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 42
- 235000013405 beer Nutrition 0.000 claims description 28
- 239000000314 lubricant Substances 0.000 claims description 28
- 239000004014 plasticizer Substances 0.000 claims description 28
- NBOCQTNZUPTTEI-UHFFFAOYSA-N 4-[4-(hydrazinesulfonyl)phenoxy]benzenesulfonohydrazide Chemical compound C1=CC(S(=O)(=O)NN)=CC=C1OC1=CC=C(S(=O)(=O)NN)C=C1 NBOCQTNZUPTTEI-UHFFFAOYSA-N 0.000 claims description 23
- 229920000642 polymer Polymers 0.000 claims description 22
- 239000004800 polyvinyl chloride Substances 0.000 claims description 21
- 229920000915 polyvinyl chloride Polymers 0.000 claims description 21
- 239000005038 ethylene vinyl acetate Substances 0.000 claims description 18
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 claims description 18
- 230000015572 biosynthetic process Effects 0.000 claims description 14
- 238000004519 manufacturing process Methods 0.000 claims description 14
- 239000000049 pigment Substances 0.000 claims description 14
- 239000004604 Blowing Agent Substances 0.000 claims description 11
- 239000012760 heat stabilizer Substances 0.000 claims description 7
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 claims description 7
- 229920005992 thermoplastic resin Polymers 0.000 claims description 7
- DQXBYHZEEUGOBF-UHFFFAOYSA-N but-3-enoic acid;ethene Chemical compound C=C.OC(=O)CC=C DQXBYHZEEUGOBF-UHFFFAOYSA-N 0.000 claims description 6
- 229920000098 polyolefin Polymers 0.000 claims description 6
- 230000000717 retained effect Effects 0.000 claims 4
- GEHJYWRUCIMESM-UHFFFAOYSA-L sodium sulfite Chemical compound [Na+].[Na+].[O-]S([O-])=O GEHJYWRUCIMESM-UHFFFAOYSA-L 0.000 abstract description 26
- 235000010265 sodium sulphite Nutrition 0.000 abstract description 13
- 150000001299 aldehydes Chemical class 0.000 abstract description 11
- LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 abstract description 10
- 235000012206 bottled water Nutrition 0.000 abstract description 9
- 238000011161 development Methods 0.000 abstract description 6
- 238000012545 processing Methods 0.000 abstract description 4
- 230000002265 prevention Effects 0.000 abstract 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 45
- 239000001301 oxygen Substances 0.000 description 45
- 229910052760 oxygen Inorganic materials 0.000 description 45
- 238000009472 formulation Methods 0.000 description 30
- GVJHHUAWPYXKBD-IEOSBIPESA-N α-tocopherol Chemical compound OC1=C(C)C(C)=C2O[C@@](CCC[C@H](C)CCC[C@H](C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-IEOSBIPESA-N 0.000 description 26
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 description 22
- 235000013361 beverage Nutrition 0.000 description 20
- 239000000047 product Substances 0.000 description 20
- 229960000984 tocofersolan Drugs 0.000 description 20
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 19
- 235000001815 DL-alpha-tocopherol Nutrition 0.000 description 19
- 239000011627 DL-alpha-tocopherol Substances 0.000 description 19
- 239000000463 material Substances 0.000 description 16
- 239000003381 stabilizer Substances 0.000 description 15
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 14
- 230000000694 effects Effects 0.000 description 13
- 235000010323 ascorbic acid Nutrition 0.000 description 10
- 229920003023 plastic Polymers 0.000 description 10
- 239000004033 plastic Substances 0.000 description 10
- 239000004698 Polyethylene Substances 0.000 description 9
- 238000011109 contamination Methods 0.000 description 8
- 229920001169 thermoplastic Polymers 0.000 description 8
- 239000000654 additive Substances 0.000 description 7
- 239000003963 antioxidant agent Substances 0.000 description 7
- 235000006708 antioxidants Nutrition 0.000 description 7
- 239000011668 ascorbic acid Substances 0.000 description 7
- 238000011156 evaluation Methods 0.000 description 7
- 229940042795 hydrazides for tuberculosis treatment Drugs 0.000 description 7
- 238000010348 incorporation Methods 0.000 description 7
- 229920005989 resin Polymers 0.000 description 7
- 239000011347 resin Substances 0.000 description 7
- 239000000377 silicon dioxide Substances 0.000 description 7
- 235000010378 sodium ascorbate Nutrition 0.000 description 7
- PPASLZSBLFJQEF-RKJRWTFHSA-M sodium ascorbate Substances [Na+].OC[C@@H](O)[C@H]1OC(=O)C(O)=C1[O-] PPASLZSBLFJQEF-RKJRWTFHSA-M 0.000 description 7
- 229960005055 sodium ascorbate Drugs 0.000 description 7
- PPASLZSBLFJQEF-RXSVEWSESA-M sodium-L-ascorbate Chemical compound [Na+].OC[C@H](O)[C@H]1OC(=O)C(O)=C1[O-] PPASLZSBLFJQEF-RXSVEWSESA-M 0.000 description 7
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 6
- RAHZWNYVWXNFOC-UHFFFAOYSA-N Sulphur dioxide Chemical compound O=S=O RAHZWNYVWXNFOC-UHFFFAOYSA-N 0.000 description 6
- 229960005070 ascorbic acid Drugs 0.000 description 6
- 238000006243 chemical reaction Methods 0.000 description 6
- 235000014113 dietary fatty acids Nutrition 0.000 description 6
- 239000000194 fatty acid Substances 0.000 description 6
- 229930195729 fatty acid Natural products 0.000 description 6
- 150000004665 fatty acids Chemical class 0.000 description 6
- 238000007789 sealing Methods 0.000 description 6
- 238000003860 storage Methods 0.000 description 6
- 238000012360 testing method Methods 0.000 description 6
- 239000012153 distilled water Substances 0.000 description 5
- 238000005516 engineering process Methods 0.000 description 5
- 235000013305 food Nutrition 0.000 description 5
- 239000007789 gas Substances 0.000 description 5
- 239000011521 glass Substances 0.000 description 5
- 239000004416 thermosoftening plastic Substances 0.000 description 5
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 4
- 239000012190 activator Substances 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- 239000000460 chlorine Substances 0.000 description 4
- 229910052801 chlorine Inorganic materials 0.000 description 4
- 229910052751 metal Inorganic materials 0.000 description 4
- 239000002184 metal Substances 0.000 description 4
- 230000003647 oxidation Effects 0.000 description 4
- 238000007254 oxidation reaction Methods 0.000 description 4
- 229920002379 silicone rubber Polymers 0.000 description 4
- 150000000994 L-ascorbates Chemical class 0.000 description 3
- 229940123973 Oxygen scavenger Drugs 0.000 description 3
- 239000004743 Polypropylene Substances 0.000 description 3
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 230000002411 adverse Effects 0.000 description 3
- 150000001408 amides Chemical class 0.000 description 3
- 239000001569 carbon dioxide Substances 0.000 description 3
- 229910002092 carbon dioxide Inorganic materials 0.000 description 3
- 239000011203 carbon fibre reinforced carbon Substances 0.000 description 3
- 238000000354 decomposition reaction Methods 0.000 description 3
- WIGCFUFOHFEKBI-UHFFFAOYSA-N gamma-tocopherol Natural products CC(C)CCCC(C)CCCC(C)CCCC1CCC2C(C)C(O)C(C)C(C)C2O1 WIGCFUFOHFEKBI-UHFFFAOYSA-N 0.000 description 3
- 239000011261 inert gas Substances 0.000 description 3
- 244000005700 microbiome Species 0.000 description 3
- 235000019645 odor Nutrition 0.000 description 3
- LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical class [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 description 3
- 150000003611 tocopherol derivatives Chemical class 0.000 description 3
- ICGLPKIVTVWCFT-UHFFFAOYSA-N 4-methylbenzenesulfonohydrazide Chemical compound CC1=CC=C(S(=O)(=O)NN)C=C1 ICGLPKIVTVWCFT-UHFFFAOYSA-N 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- GZIFEOYASATJEH-UHFFFAOYSA-N D-delta tocopherol Natural products OC1=CC(C)=C2OC(CCCC(C)CCCC(C)CCCC(C)C)(C)CCC2=C1 GZIFEOYASATJEH-UHFFFAOYSA-N 0.000 description 2
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 2
- 239000004809 Teflon Substances 0.000 description 2
- 229920006362 Teflon® Polymers 0.000 description 2
- 229930003427 Vitamin E Natural products 0.000 description 2
- 239000002250 absorbent Substances 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 230000000996 additive effect Effects 0.000 description 2
- 229910052783 alkali metal Inorganic materials 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- 230000003078 antioxidant effect Effects 0.000 description 2
- 238000013459 approach Methods 0.000 description 2
- 229940072107 ascorbate Drugs 0.000 description 2
- 239000012298 atmosphere Substances 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 2
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 2
- 210000004027 cell Anatomy 0.000 description 2
- 239000000356 contaminant Substances 0.000 description 2
- 230000001627 detrimental effect Effects 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 238000004821 distillation Methods 0.000 description 2
- 239000003814 drug Substances 0.000 description 2
- 239000000835 fiber Substances 0.000 description 2
- 235000021554 flavoured beverage Nutrition 0.000 description 2
- 239000006260 foam Substances 0.000 description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 2
- 238000002386 leaching Methods 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 238000000465 moulding Methods 0.000 description 2
- 239000007800 oxidant agent Substances 0.000 description 2
- 230000001590 oxidative effect Effects 0.000 description 2
- 238000004806 packaging method and process Methods 0.000 description 2
- 229920000139 polyethylene terephthalate Polymers 0.000 description 2
- 239000005020 polyethylene terephthalate Substances 0.000 description 2
- 229920002635 polyurethane Polymers 0.000 description 2
- 239000004814 polyurethane Substances 0.000 description 2
- 239000002243 precursor Substances 0.000 description 2
- 230000002000 scavenging effect Effects 0.000 description 2
- 239000004945 silicone rubber Substances 0.000 description 2
- 229940046009 vitamin E Drugs 0.000 description 2
- 235000019165 vitamin E Nutrition 0.000 description 2
- 239000011709 vitamin E Substances 0.000 description 2
- WGVKWNUPNGFDFJ-DQCZWYHMSA-N β-tocopherol Chemical compound OC1=CC(C)=C2O[C@@](CCC[C@H](C)CCC[C@H](C)CCCC(C)C)(C)CCC2=C1C WGVKWNUPNGFDFJ-DQCZWYHMSA-N 0.000 description 2
- QUEDXNHFTDJVIY-UHFFFAOYSA-N γ-tocopherol Chemical compound OC1=C(C)C(C)=C2OC(CCCC(C)CCCC(C)CCCC(C)C)(C)CCC2=C1 QUEDXNHFTDJVIY-UHFFFAOYSA-N 0.000 description 2
- GZIFEOYASATJEH-VHFRWLAGSA-N δ-tocopherol Chemical compound OC1=CC(C)=C2O[C@@](CCC[C@H](C)CCC[C@H](C)CCCC(C)C)(C)CCC2=C1 GZIFEOYASATJEH-VHFRWLAGSA-N 0.000 description 2
- WGVKWNUPNGFDFJ-UHFFFAOYSA-N 2,5,8-Trimethyl-2-(4,8,12-trimethyltridecyl)-6-chromanol Chemical compound OC1=CC(C)=C2OC(CCCC(C)CCCC(C)CCCC(C)C)(C)CCC2=C1C WGVKWNUPNGFDFJ-UHFFFAOYSA-N 0.000 description 1
- GWXXFGWOWOJEEX-UHFFFAOYSA-N 4,4,4-trihydroxy-1-phenylbutan-1-one Chemical compound OC(CCC(=O)C1=CC=CC=C1)(O)O GWXXFGWOWOJEEX-UHFFFAOYSA-N 0.000 description 1
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 1
- 240000008100 Brassica rapa Species 0.000 description 1
- 239000004255 Butylated hydroxyanisole Substances 0.000 description 1
- 239000004322 Butylated hydroxytoluene Substances 0.000 description 1
- NLZUEZXRPGMBCV-UHFFFAOYSA-N Butylhydroxytoluene Chemical compound CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 NLZUEZXRPGMBCV-UHFFFAOYSA-N 0.000 description 1
- OCUCCJIRFHNWBP-IYEMJOQQSA-L Copper gluconate Chemical class [Cu+2].OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C([O-])=O.OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C([O-])=O OCUCCJIRFHNWBP-IYEMJOQQSA-L 0.000 description 1
- ZZZCUOFIHGPKAK-UHFFFAOYSA-N D-erythro-ascorbic acid Natural products OCC1OC(=O)C(O)=C1O ZZZCUOFIHGPKAK-UHFFFAOYSA-N 0.000 description 1
- CIWBSHSKHKDKBQ-DUZGATOHSA-N D-isoascorbic acid Chemical compound OC[C@@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-DUZGATOHSA-N 0.000 description 1
- CWYNVVGOOAEACU-UHFFFAOYSA-N Fe2+ Chemical compound [Fe+2] CWYNVVGOOAEACU-UHFFFAOYSA-N 0.000 description 1
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 239000002211 L-ascorbic acid Substances 0.000 description 1
- 235000000069 L-ascorbic acid Nutrition 0.000 description 1
- 229920001944 Plastisol Polymers 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- 101100386054 Saccharomyces cerevisiae (strain ATCC 204508 / S288c) CYS3 gene Proteins 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- 229930003268 Vitamin C Natural products 0.000 description 1
- 230000002745 absorbent Effects 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 125000003342 alkenyl group Chemical group 0.000 description 1
- 229940087168 alpha tocopherol Drugs 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 229940053200 antiepileptics fatty acid derivative Drugs 0.000 description 1
- 150000001491 aromatic compounds Chemical class 0.000 description 1
- 150000005840 aryl radicals Chemical group 0.000 description 1
- 230000004888 barrier function Effects 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 229940066595 beta tocopherol Drugs 0.000 description 1
- WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- 235000019282 butylated hydroxyanisole Nutrition 0.000 description 1
- CZBZUDVBLSSABA-UHFFFAOYSA-N butylated hydroxyanisole Chemical compound COC1=CC=C(O)C(C(C)(C)C)=C1.COC1=CC=C(O)C=C1C(C)(C)C CZBZUDVBLSSABA-UHFFFAOYSA-N 0.000 description 1
- 229940043253 butylated hydroxyanisole Drugs 0.000 description 1
- 235000010354 butylated hydroxytoluene Nutrition 0.000 description 1
- 229940095259 butylated hydroxytoluene Drugs 0.000 description 1
- 235000013877 carbamide Nutrition 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 210000003850 cellular structure Anatomy 0.000 description 1
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- 238000006392 deoxygenation reaction Methods 0.000 description 1
- 239000002274 desiccant Substances 0.000 description 1
- 239000000645 desinfectant Substances 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 235000015872 dietary supplement Nutrition 0.000 description 1
- 229910001873 dinitrogen Inorganic materials 0.000 description 1
- 235000020188 drinking water Nutrition 0.000 description 1
- 239000003651 drinking water Substances 0.000 description 1
- 239000002384 drinking water standard Substances 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 235000010350 erythorbic acid Nutrition 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000011049 filling Methods 0.000 description 1
- 238000005429 filling process Methods 0.000 description 1
- 239000005308 flint glass Substances 0.000 description 1
- 235000010382 gamma-tocopherol Nutrition 0.000 description 1
- 238000013023 gasketing Methods 0.000 description 1
- 239000008103 glucose Substances 0.000 description 1
- 229960001031 glucose Drugs 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 230000036541 health Effects 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229920001903 high density polyethylene Polymers 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 239000010954 inorganic particle Substances 0.000 description 1
- 229940026239 isoascorbic acid Drugs 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 239000012263 liquid product Substances 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
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- ZIUHHBKFKCYYJD-UHFFFAOYSA-N n,n'-methylenebisacrylamide Chemical compound C=CC(=O)NCNC(=O)C=C ZIUHHBKFKCYYJD-UHFFFAOYSA-N 0.000 description 1
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- 150000002978 peroxides Chemical class 0.000 description 1
- 239000000825 pharmaceutical preparation Substances 0.000 description 1
- 229940127557 pharmaceutical product Drugs 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 239000004999 plastisol Substances 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 238000004537 pulping Methods 0.000 description 1
- 239000005060 rubber Substances 0.000 description 1
- 239000003566 sealing material Substances 0.000 description 1
- 238000007493 shaping process Methods 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 235000014214 soft drink Nutrition 0.000 description 1
- 230000000707 stereoselective effect Effects 0.000 description 1
- 101150035983 str1 gene Proteins 0.000 description 1
- 150000003460 sulfonic acids Chemical class 0.000 description 1
- 230000009897 systematic effect Effects 0.000 description 1
- 239000012815 thermoplastic material Substances 0.000 description 1
- 235000019149 tocopherols Nutrition 0.000 description 1
- 150000004670 unsaturated fatty acids Chemical class 0.000 description 1
- 235000021122 unsaturated fatty acids Nutrition 0.000 description 1
- 150000003672 ureas Chemical class 0.000 description 1
- 238000009489 vacuum treatment Methods 0.000 description 1
- 235000019154 vitamin C Nutrition 0.000 description 1
- 239000011718 vitamin C Substances 0.000 description 1
- 235000004835 α-tocopherol Nutrition 0.000 description 1
- 239000002076 α-tocopherol Substances 0.000 description 1
- 235000007680 β-tocopherol Nutrition 0.000 description 1
- 239000011590 β-tocopherol Substances 0.000 description 1
- QUEDXNHFTDJVIY-DQCZWYHMSA-N γ-tocopherol Chemical compound OC1=C(C)C(C)=C2O[C@@](CCC[C@H](C)CCC[C@H](C)CCCC(C)C)(C)CCC2=C1 QUEDXNHFTDJVIY-DQCZWYHMSA-N 0.000 description 1
- 239000002478 γ-tocopherol Substances 0.000 description 1
- 239000002446 δ-tocopherol Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/04—Oxygen-containing compounds
- C08K5/15—Heterocyclic compounds having oxygen in the ring
- C08K5/151—Heterocyclic compounds having oxygen in the ring having one oxygen atom in the ring
- C08K5/1545—Six-membered rings
-
- A—HUMAN NECESSITIES
- A47—FURNITURE; DOMESTIC ARTICLES OR APPLIANCES; COFFEE MILLS; SPICE MILLS; SUCTION CLEANERS IN GENERAL
- A47J—KITCHEN EQUIPMENT; COFFEE MILLS; SPICE MILLS; APPARATUS FOR MAKING BEVERAGES
- A47J41/00—Thermally-insulated vessels, e.g. flasks, jugs, jars
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B65—CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
- B65D—CONTAINERS FOR STORAGE OR TRANSPORT OF ARTICLES OR MATERIALS, e.g. BAGS, BARRELS, BOTTLES, BOXES, CANS, CARTONS, CRATES, DRUMS, JARS, TANKS, HOPPERS, FORWARDING CONTAINERS; ACCESSORIES, CLOSURES, OR FITTINGS THEREFOR; PACKAGING ELEMENTS; PACKAGES
- B65D53/00—Sealing or packing elements; Sealings formed by liquid or plastics material
- B65D53/06—Sealings formed by liquid or plastic material
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/30—Sulfur-, selenium- or tellurium-containing compounds
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/0008—Organic ingredients according to more than one of the "one dot" groups of C08K5/01 - C08K5/59
- C08K5/005—Stabilisers against oxidation, heat, light, ozone
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/36—Sulfur-, selenium-, or tellurium-containing compounds
- C08K5/43—Compounds containing sulfur bound to nitrogen
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/13—Hollow or container type article [e.g., tube, vase, etc.]
- Y10T428/1352—Polymer or resin containing [i.e., natural or synthetic]
- Y10T428/1397—Single layer [continuous layer]
Definitions
- the present invention relates to plastic compositions that are intended for use as liners in closures for potable fluid containers such as bottled water and beer.
- the liner includes certain additive compositions that protect against the development during processing of the liner and the container of off-flavor in the potable fluid that would otherwise result from the reaction of oxygen with the plastic liner composition or components thereof.
- thermoplastic liner material directly in the crown which will later be used for bottling beer or other beverages.
- liners are primarily made of polyvinyl chloride ("PVC") in the United States and of thermoplastics that do not contain chlorine, such as EVA or polyethylene (“PE”), in Europe and Japan.
- PVC polyvinyl chloride
- PE polyethylene
- a conventional apparatus for making lined crowns is the Za-Matic® Model 1400A (available from ZapatA Industries, Inc.) described in U.S. Pat. Nos. 3,135,019, 3,360,827, and 3,577,595.
- the liner compositions may be based upon plastics such as, for instance, PVC, EVA, or PE, and may include those of U.S. Pat. No. 3,547,746.
- PVC compositions with or without additives as stabilizers or for imparting certain properties are known in the art.
- U.S. Pat. No. 4,380,597 discloses a stabilized thermoplastic composition of OVC or mixed polymers that may include ascorbates or gluconates as stabilizer additives. These stabilizers are added not to absorb oxygen from inside packages made of the polymer but to prevent breakdown of the polymer itself.
- U.S. Pat. No. 4,211,681 discloses shaped articles, for instance films or tubes, that include high molecular weight poly(ethylene oxide) polymers with stabilizers of ascorbic acid, 2,3-butylhydroxyanisoles, and the like. Japanese Patent Application No.
- 62-215,101 discloses a deodorizing fiber obtained by treating thermoplastic fibers with inorganic particles of divalent ferrous iron and L-ascorbic acid.
- U.S. Pat. No. 4,278,718 discloses a sealing composition for beverage containers consisting of a vinyl chloride resin, a plasticizer, and a metal oxide.
- hydrazides such as OBSH
- Blowing agents are chemicals that are added to plastics or rubbers for generating inert gas upon decomposition, causing the resin to assume a cellular structure.
- OBSH 4-4'-oxybis (benzenesulfonyl hydrazide)
- OBSH 4-4'-oxybis (benzenesulfonyl hydrazide)
- liners for most beverage closures are based either on PVC or EVA, although other materials have been used too.
- U.S. Pat. No. 4,968,514 teaches that polyurethanes can be used to make liners for metal-shelled beer bottle crown caps. These polymer bases can be compounded to give adequate processing properties and product performance, utilizing among other additives heat stabilizers, antioxidants, and lubricants.
- Naturally occurring fatty acids are often used as lubricants in liner formulations. Fatty acids are separated into individual products and purified by distillation. Because of the wide range of individual acids occurring in nature, a distillation fraction will contain several fatty acids. Some of the impurities contain unsaturation at the 4-, 5-, 6-, 7-, or 8-carbon position.
- the fatty acids are converted to ester or amide derivatives which likewise contain mid-chain unsaturation.
- the fatty acid derivatives are subject to oxidation at the mid-chain unsaturation by oxygen or other oxidizing agents in the beverage or in the air that is enclosed along with the beverage in the container.
- Oxidation results in aldehydes, some of which have very low flavor thresholds.
- Such liners are adequate for many beverage products in that their contribution of off-flavor to the beverage is not noticeable.
- the polymeric cap liner of the container is a source of double-bond containing precursors that react with oxygen in bottled water.
- Polymeric cap liners typically contain a number of plasticizers, heat stabilizers, lubricants, antioxidants, blowing agents, and pigments, some or all of which contain double bonds that are susceptible to attack by oxygen.
- the liner formulations for twist-off caps typically comprise oleamide-type lubricants. The double bonds in such oleamides are readily susceptible to attack by oxygen, resulting in off-flavored producing medium-chain-length aldehydes.
- fatty acids or derivatives of fatty acids of liner compositions react with oxygen to form off-flavored aldehydes.
- Other compounds often found in polymeric cap liners which are susceptible to attack from oxygen include activated aromatic compounds such as phenols, and other double bond containing compounds such as ketones, amides, crucic acid, etc.
- the resulting aldehydes are responsible for the fruity tastes and odors often found in bottled water.
- ozone as a disinfectant instead of chlorine to kill any microorganisms present in the water itself.
- the bottled water usually contains ozone in trace amounts.
- ozone is present in an amount of about 0.1 to 0.4 mg/l. These trace amounts kill the microorganisms so that is it not necessary for the water to be pasteurized.
- ozone oxidizes many nuisance compounds or contaminants in water supplies.
- Drinking water standards in the United States specify that drinking water should not have any smell or taste.
- C. Anselme et al. in J. American Waterworks Association, 80, 45-51 (1988) the intensity of a fruity off-flavor correlates strongly with the total concentration of aldehydes present in the water.
- Ozone also reacts with compounds which contain double bonds, such as alkenes, yielding corresponding aldehydes as the major oxidation product.
- aldehydes are responsible for the fruity tastes and odors that are found in bottled water.
- oxygen contamination can be particularly troublesome. Care is generally taken to minimize the introduction of oxygen or to reduce the detrimental or undesirable effects of oxygen on the product.
- Carbon-carbon double bonds are particularly susceptible to reaction with active oxygen species. Such carbon-carbon bonds are often found in foods and beverages, pharmaceuticals, dyes, photochemicals, adhesives, and polymer precursors. Virtually any product that has complex organic constituents will contain such carbon-carbon double bonds or other oxygen-reactive components, and hence can undergo oxidative reactions.
- One usual technique is to remove the air via vacuum from a clean bottle, fill the bottle with carbon dioxide, flow the beer down the bottle wall into the bottle thus displacing the carbon dioxide, and finally squirting a jet of high-pressure deoxygenated water into the bottle to cause the beer to over-foam just as the cap is put on, thereby attempting to displace the remaining headspace gases with the beer's own carbon dioxide.
- production lines are run slowly in order to minimize the introduction of air into the headspace just before capping. All of this is expensive, and usually reduces the total oxygen concentration in the headspace to about 200-400 parts per billion.
- the 200-400 ppb achieved in the packaged product by careful brewers corresponds to approximately 50-100 microliters of oxygen per 355 ml bottle. Even this small quantity of oxygen is still considered to be one of the major limitations on quality and shelf life of beer today.
- the desired level is as close to zero as possible, but certainly below about 50 ppb.
- U.S. Pat. No. 4,279,350 discloses a closure liner that incorporates a catalyst disposed between an oxygen-permeable barrier and a water-absorbent backing layer.
- U.K. Patent Application No. 2,040,889 discloses a closure in the form of a stopper molded from ethylene vinyl acetate ("EVA") having a closed-cell foamed core that may contain water and sulfur dioxide to act as an oxygen scavenger and a liquid-impervious skin.
- EVA ethylene vinyl acetate
- 328,336 and 328,337 disclose container closure elements, such as caps, removable panels, liners, or sealing compositions that are formed of a polymeric matrix containing an oxygen scavenger therein.
- U.S. Pat. No. 4,287,995 discloses a sealing member for a container that is used to preserve aqueous liquids therein. This sealing member is mounted on the cap or stopper of the container on the portion facing the contents.
- the sealing member contains an oxygen absorbent that is separated from contacting the contents of the container by a film that has a plurality of fine openings such that it is gas-permeable but water-impermeable at one atmosphere pressure.
- U.S. Pat. No. 5,143,763 describes an approach that prevents oxygen deterioration in containerized substances that relies on the absorption of oxygen from within the container. This patent does not teach how to prevent the containerized substances from developing off flavor that is due to leaching substances from the liner.
- the present invention protects containerized beverages such as beer and water from developing off-flavor due to leaching of aldehydes from the crown liner.
- This invention is directed to a liner composition for a closure element of a container for potable fluids such as water.
- the liner composition includes at least an inorganic sulfite compound or a tocopherol compound in amount sufficient to protect against the development of off-flavor in a potable fluid in the container.
- the preferred inorganic sulfite compound is a sulfite salt such as sodium sulfite.
- the preferred tocopherol compound is dl- ⁇ -tocopherol.
- the invention is also directed to a potable fluid container comprising a reservoir element for containing fluid, which element has an opening, a closure element capable of being attached to the opening, and the above-described liner composition associated with the closure element.
- the closure has a recessed portion for receiving the container opening, and the liner is placed within the recess of the closure element between the container opening and the closure element for sealing the fluid within the container.
- Another aspect of the invention relates to a method of improving the taste of a bottled fluid such as water by containing the fluid in the above potable fluid container and associating the above liner composition with the container so that the inorganic sulfite compound or tocopherol compound can react with residual oxygen in the headspace.
- Still another aspect of the present invention is a method of making a liner composition for a potable-fluid-container closure element that comprises combining a thermoplastic polymer with a first flavor protectant compound of an inorganic sulfite compound or a tocopherol compound in an amount sufficient to prevent or inhibit the formation in the liner composition of off-flavor-causing substances and subsequently shaping a portion of said thermoplastic polymer into a shape that will enable it to function as a liner for a closure element and affixing said shaped thermoplastic polymer into place in or on said closure element.
- This invention relates in part to container closures for use in combination with means for retaining a water-containing foodstuff, beverage, chemical, or pharmaceutical product, which retaining means has a least one opening therein for filling or dispensing of the product.
- These container closures include a member for closing the opening of the retaining means and preventing escape of the liquid product when not desired, and a liner or gasket comprising one of the flavor protectant compositions described above being positioned adjacent the closing member.
- the retaining means is a can, jar, or bottle of metal, glass, or plastic construction
- the closing member is a crown or closure.
- polymers may be used in accordance with the teaching of the present invention.
- the polymer is preferably a polymeric thermoplastic, such as PVC, EVA, polyethylene terephthalate (“PET”), PE, or polypropylene (“PP”), or a polyurethane.
- PVC polymeric thermoplastic
- EVA polyethylene terephthalate
- PE polyethylene terephthalate
- PE polypropylene
- U.S. Pat. No. 3,547,746 provides much useful disclosure about these and thus is expressly incorporated herein by reference.
- the PVC resins that are preferred for use as the polymer in the flavor protectant compositions of the invention are set forth in the patent at column 2, lines 35-47. This patent also discloses suitable plasticizer compounds that may be used with the thermoplastic resin along with preferred ranges thereof.
- an amount of plasticizer ranging from about 60 to 90 parts by weight based on 100 parts by weight of the polymer for crown liners. Depending upon the specific product to be made, the amount of plasticizer can vary from 10 to 120 parts. Specific plasticizers for PVC crown liners are recited in column 5, lines 49-53 of the patent.
- the polymer should have a rate of water vapor transmission of between 0.05 and 25 g-mm/m 2 /24 hours at 37.8° C.
- PVC typically provides a value of 2-12, PE between 0.1 and 1, and EVA 0.8 to 1.2. These rates are sufficient to enable the water vapor to permeate the polymer to activate the flavor protectant materials therein.
- the polymer should also be permeable to oxygen and have a permeability rate of between 50 and 2000, and preferably between 100 and 1500 cc-mil/100 square inches/24 hours per atmosphere pressure at 25° C.
- PVC provides values between 100-1400, PE about 185-500, and EVA about 830-850.
- the liner composition comprises a first flavor protectant agent that is either an inorganic sulfite compound or a tocopherol compound in an amount sufficient to protect against the development of off-flavor in a potable fluid in the container.
- the inorganic sulfite compound may be an alkaline earth metal sulfite or an alkali metal sulfite.
- the alkali metal salts such as sodium sulfite are preferred.
- sodium sulfite is a well-known and versatile chemical.
- tocopherol compounds can be used.
- the compound dl- ⁇ -tocopherol, also known as vitamin E, is structurally identified as 2,5,7,8-tetramethyl-2-(4',8',12'-trimethyltridecyl)-6-chromanol.
- dl- ⁇ -tocopherol or vitamin E
- other tocopherol compounds including not only the stereospecific isomers of ⁇ -tocopherol but also ⁇ -tocopherol, i.e., 2,5,8-trimethyl-2-(4',8',12'-trimethyltridecyl)-6-chromanol
- ⁇ -tocopherol i.e., 2,7,8-trimethyl-2-(4',8',12'-trimethyltridecyl)-6-chromanol
- ⁇ -tocopherol i.e., 2,8-dimethyl-2-(4',8',12'-trimethyltridecyl)-6-chromanol
- 2,8-dimethyl-2-(4',8',12'-trimethyltridecyl)-6-chromanol may also be used in accordance with the present invention.
- dl- ⁇ -tocopherol is marketed, for instance by Roche under the name RONOTEC 201, as an antioxidant in polymers and oils.
- RONOTEC 201 an antioxidant in polymers and oils.
- dl- ⁇ -tocopherol could be used in liner formulations to protect the flavor of containerized beverages.
- the inorganic sulfite compounds and tocopherol compounds for use in the liners of the present invention should be compatible with the material and other components of the liner and approved by the FDA for use in contact with the fluid to be ingested.
- the inorganic sulfite compound is present in the liner composition in an amount of from about 0.3 to about 5%, and more preferably 0.5 to 3%, by weight of the composition, while the tocopherol compound is present in the liner composition in an amount of from about 0.3 to about 3%, and more preferably 0.5 to 1%, by weight of the composition.
- the liner composition is generally made of a material which is permeable to gases and water or water vapor.
- this material would typically be a polymer, such as a thermoplastic resin.
- Thermoplastic resins of polyolefins such as PE and the like, PVC, EVA, and the like would allow gases such as oxygen or ozone, and water or water vapor to pass into and through the liner.
- the inorganic sulfite or tocopherol of the present invention protects against the development of off-flavors which would otherwise result from the formation of aldehydes due to the reaction of oxygen sources present in the potable fluid with prior art liner compositions or components thereof.
- flavor protectant compound While it is contemplated in accordance with the present invention to use a single flavor protectant compound, it is often preferable to use a combination of flavor protectant compounds. The most preferred combination would be a sulfite compound and a tocopherol compound. However, additional flavor protectant compounds can often advantageously be used along with the inorganic sulfites or tocopherols according to the present invention, however. Generally, the second flavor protectant compound can be used in an amount of between about 0.1 and 5% by weight. Typical examples of such additional compounds include 1 to 2% by weight of an ascorbate such as sodium ascorbate and 1 to 3% by weight of a hydrazide compound.
- the preferred hydrazide is a sulfonyl hydrazide such as OBSH or p-toluene sulfonyl hydrazide.
- Carboxylic acid hydrazides can also be used.
- the use of hydrazides is disclosed in commonly assigned application Ser. No. 08/167,257, the content of which is expressly incorporated herein by reference thereto.
- the use of ascorbates such as vitamin C and related compounds (e.g., sodium ascorbate) is disclosed in U.S. Pat. No. 5,202,052, the content of which is also expressly incorporated herein by reference thereto.
- the hydrazide compound is an "unactivated hydrazide,” i.e., a hydrazide compound which has not been subjected to a decomposition reaction. This can occur by either adding an amount of a hydrazide compound beyond that which is needed for use as a blowing agent or by processing the liner so as to not decompose the hydrazide compound which is present.
- Hydrazides of organic sulfonic acids have been found to be useful in the present invention. Both aliphatic and aromatic sulfonic acids can be used, with one or both --NH 2 groups of the hydrazine molecule being substituted with alkyl or aryl radicals.
- the most preferred compound is a sulfonyl hydrazide, such as OBSH, since it has FDA approval for applications and articles which come into contact with food or beverages.
- Other sulfonyl hydrazides such s p-toluene sulfonyl hydrazide can be used, if desired.
- the useful hydrogens may optionally be substituted by other organic moieties.
- the hydrazide compound be compatible with the material and other components of the liner and that the compound be FDA approved for use in contact with the fluid to be ingested.
- the hydrazide compound may be present in the liner composition in an amount of from about 0.1 to about 1% by weight of the composition.
- the liner composition may also include a hydrazide compound for use as a blowing agent
- the composition must be formulated so that the amount of hydrazide compound that is decomposed is less than the total amount of hydrazide compound that is added to the liner composition.
- This decomposition may be activated by an activator or by heat.
- an activator for decomposing the hydrazide compound is added in an amount that is less than that necessary to activate the total amount of hydrazide compound in the liner composition.
- typical activators include carbonates, glycols, ureas, acids, alkanolamines, oxidizing agents such as peroxides. In particular, carbonates such as sodium carbonate are preferred activators.
- the present invention may also include at least one blowing agent other than the unactivated hydrazide compound, if desired.
- compositions of the invention are as liners or gaskets in crowns or closures for capping beverage bottles. Entire closures may also be made of plastics containing compositions of the invention, for instance all plastic screw-on threaded caps for soft drink bottles, and the like.
- Another preferred use of the composition of the invention is as a gasket or liner applied to an aluminum or plastic closure or metal crown for plastic or glass bottles.
- thermoplastic material such as PVC or EVA
- polyolefins such as PE or PP
- these materials are formulated to include plasticizers, heat stabilizers, lubricants, blowing agents, antioxidants, pigments, and other additives.
- plasticizers heat stabilizers, lubricants, blowing agents, antioxidants, pigments, and other additives.
- PVC liners are well known for use in crowns as described in the production of crowns using the Za-Matic machines. There is also well know technology for making aluminum or plastic closures containing EVA liners. The disclosure of U.S. Pat. No. 3,547,746 is likewise useful for its teachings of crown liner manufacturing techniques, and thus is expressly incorporated herein by reference thereto on this point as well.
- this crown liner manufacturing method which is generally used for PVC, EVA, or PE liners
- many other devices can apply liners by plastisol spin-lining or various hot molding techniques.
- the present invention is easily applicable to both gasketing/coating/sealing materials for metal crowns or closures, such as beer bottle crown or soda closure liners, and to containers or closures comprised primarily of plastic materials.
- Formulations according to the present invention may be prepared for use in a Za-Matic machine for application as a liner to a beer bottle crown.
- the PVC resin is placed in a dry mix kettle, and plasticizer is added with continuous heating and mixing. All other additives, including the flavor protectant material, are then gradually introduced into the resin to form a dry blend. This dry blend is place into an extruder and pelletized to form the liner compound that is added to the Za-Matic machine to form liners on metal bottle crowns.
- U.S. Pat. No. 5,202,052 describes this and other liner manufacturing procedures that may be adapted by those skilled in the art to manufacture the liners of the present invention.
- the inorganic sulfite compound or tocopherol compound may be admixed into the liner or can be coated thereon or otherwise associated therewith.
- the potable fluid container of the present invention contains a potable fluid, most preferably beer or water.
- the potable fluid container has ozone added thereto.
- the ozone is preferably added in trace amounts, such as from about 0.1 to 0.5 mg/l.
- test samples were prepared and compared to controls. It is emphasized that the taste of the water, even though it has important commercial consequences, may be regarded as an indicator of the presence in the liners of extractable off-flavor-causing substances.
- a fresh control was prepared for each experiment.
- a panel of trained flavor tasters evaluated the samples along with an outside consultant.
- the liner materials were evaluated for improved flavor over the control after one day and long term storage.
- the bottles were pasteurized at 140° F. for 20 minutes, cooled to 90° F., and stored at room temperature for various periods of time, up to sixteen days. After the storage period, the water was evaluated by the flavor panel for any off-flavors. The intensity of the off-flavor was scored by each panelist on a scale of 0 (No detectable off-flavor) to 3 (intense off-flavor). The individual panelists scores were averaged to determine the panel's overall score for each product. The control was prepared in the same manner as the test samples.
- Seven 200 ml water samples were each ozonized as follows. Seven samples of 206 ⁇ 0.5 grams of distilled water were each poured into a clean 7 ounce bottle. A Sander Ozonizer Model 25, having 25 mg per hour capacity was connected to a 100% oxygen tank via a silicone rubber tubing. The outlet of the ozonizer was connected to Teflon tubing via silicon rubber tubing to minimize the exposure of the silicon rubber to the ozone. The Teflon Tubing was connected to a glass gas dispersion tube, Catalog Number 9435A of Ace Glass, Inc., Vineland, N.J., via silicone rubber tubing. The glass gas dispersion rube was immersed in water. The ozone concentration was controlled with oxygen flow and flow time.
- the components of the liner are the source of off-flavor in the water samples.
- the components are separately added to the samples, each in an amount of 2 mg.
- the composition of the liner is given below in Table 8.
- Lubricant #1 and lubricant #2 are amides of an unsaturated fatty acid, and lubricant #3 is a paraffin wax.
- a seventh sample was used as a control, having nothing added thereto. The bottles were immediately crowned and later tested for flavor.
- the final ozone concentration before crowning was determined to be 0.4 to 0.5 mg/l.
- the bottles were stored at room temperature for two days. Calorimetric analysis showed that the control sometimes contained unreacted ozone after two days, while no ozone remained in any of the bottles to which the additional components had been added.
- the samples were then evaluated by a taste panel, evaluating the off-flavor intensity of the samples.
- the results were such that the sample containing OBSH and the control had approximately the same flavor, which flavor was less than for the samples containing the secondary plasticizer and the lubricants, with the sample containing lubricant #2 having the strongest flavor of all the samples evaluated.
- Example 18 Three samples of distilled water were bubbled with ozone as in Example 18 to contain a concentration of 0.4-0.5 mg/l ozone and then were crowned in a bottle with the following liners having the following formulations:
- the bottles were stored for 56 days at 30° C. and were evaluated for off-flavor by a taste panel.
- the results were as follows:
- the OBSH containing sample was found to be clearly superior to the other samples.
- Example 18 Three bottles of distilled water were ozonized as in Example 18 to contain 0.4 mg/l ozone. The bottles were capped with the following closure tapes which were made from a copolymer of ethylene vinyl acetate comprising of 10% vinyl acetate having the following formulations:
- CT-1 had weak off-flavor intensity
- CT-2 had moderate off-flavor intensity
- CT-3 had no off-flavor intensity
- Example 18 Six bottles of water were ozonized as in Example 18 to contain a concentration of 0.4-0.5 mg/l ozone. The bottles were sealed with crown liner elements 18, 19, 19+(0.2% OBSH) and with closure tapes CT-1, CT-2, and CT-3. The bottles were then heated at 30° C. for 30 days. A taste panel then evaluated that taste of each sample for off-flavor intensity on a scale of 0-3, with 0 having no off-flavor and 3 having an intense off-flavor. The results are as follows.
- Example 18 Three bottles of water were ozonized as in Example 18 to maintain a concentration of 0.4 mg/l of ozone.
- the bottles were sealed with the following crown liner elements.
- the bottles were stored for 5 days at room temperature and were evaluated for off-flavor by a taste panel.
- Formulation 25 containing 0.5% OBSH based on the total weight of the liner formulation, was unanimously rated the best by the panel.
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- Anti-Oxidant Or Stabilizer Compositions (AREA)
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- Non-Alcoholic Beverages (AREA)
Abstract
A liner composition for a potable fluid container closure element which includes an inorganic sulfite such as sodium sulfite and/or a tocopherol compound such as a dl-α-tocopherol (vitamin E) for preventing off-flavors due to the presence of aldehydes in the fluid. Also, a potable fluid container of a reservoir element for containing a potable fluid, the reservoir element having an opening, a closure element capable of being attached to the opening, and the liner composition associated with the closure element. Also, a method of improving the taste of a potable fluid such as bottled water by use of the container and one of the previously described liner compositions associated therewith. Also, an improved method for processing the composition into closure liners based upon the prevention of the development of off-flavor-causing substances therein.
Description
This is a continuation of application Ser. No. 08/289,170, filed Aug. 11, 1994, now U.S. Pat. No. 5,663,223.
The present invention relates to plastic compositions that are intended for use as liners in closures for potable fluid containers such as bottled water and beer. The liner includes certain additive compositions that protect against the development during processing of the liner and the container of off-flavor in the potable fluid that would otherwise result from the reaction of oxygen with the plastic liner composition or components thereof.
Crown liner technology
Current crown liner technology includes the in situ molding of a thermoplastic liner material directly in the crown which will later be used for bottling beer or other beverages. Such liners are primarily made of polyvinyl chloride ("PVC") in the United States and of thermoplastics that do not contain chlorine, such as EVA or polyethylene ("PE"), in Europe and Japan. A conventional apparatus for making lined crowns is the Za-Matic® Model 1400A (available from ZapatA Industries, Inc.) described in U.S. Pat. Nos. 3,135,019, 3,360,827, and 3,577,595. The liner compositions may be based upon plastics such as, for instance, PVC, EVA, or PE, and may include those of U.S. Pat. No. 3,547,746.
PVC compositions with or without additives as stabilizers or for imparting certain properties are known in the art. For instance, U.S. Pat. No. 4,380,597 discloses a stabilized thermoplastic composition of OVC or mixed polymers that may include ascorbates or gluconates as stabilizer additives. These stabilizers are added not to absorb oxygen from inside packages made of the polymer but to prevent breakdown of the polymer itself. U.S. Pat. No. 4,211,681 discloses shaped articles, for instance films or tubes, that include high molecular weight poly(ethylene oxide) polymers with stabilizers of ascorbic acid, 2,3-butylhydroxyanisoles, and the like. Japanese Patent Application No. 62-215,101 discloses a deodorizing fiber obtained by treating thermoplastic fibers with inorganic particles of divalent ferrous iron and L-ascorbic acid. U.S. Pat. No. 4,278,718 discloses a sealing composition for beverage containers consisting of a vinyl chloride resin, a plasticizer, and a metal oxide.
It is known to use hydrazides such as OBSH as a blowing agent in the liner composition of a closure element of a potable fluid container. Blowing agents are chemicals that are added to plastics or rubbers for generating inert gas upon decomposition, causing the resin to assume a cellular structure. For example, adding 4-4'-oxybis (benzenesulfonyl hydrazide) ("OBSH") to the liner of a closure element of a container for bottled beverage and decomposing the OBSH to produce small bubbles (foam) of nitrogen gas which are trapped inside the liner provides a sponginess to the material. When used as a liner of a closure element of the container, an improved seal is achieved.
The liners for most beverage closures are based either on PVC or EVA, although other materials have been used too. For instance, U.S. Pat. No. 4,968,514 teaches that polyurethanes can be used to make liners for metal-shelled beer bottle crown caps. These polymer bases can be compounded to give adequate processing properties and product performance, utilizing among other additives heat stabilizers, antioxidants, and lubricants. Naturally occurring fatty acids are often used as lubricants in liner formulations. Fatty acids are separated into individual products and purified by distillation. Because of the wide range of individual acids occurring in nature, a distillation fraction will contain several fatty acids. Some of the impurities contain unsaturation at the 4-, 5-, 6-, 7-, or 8-carbon position. The fatty acids are converted to ester or amide derivatives which likewise contain mid-chain unsaturation. When used as lubricants in liner formulations, the fatty acid derivatives are subject to oxidation at the mid-chain unsaturation by oxygen or other oxidizing agents in the beverage or in the air that is enclosed along with the beverage in the container. Such oxidation results in aldehydes, some of which have very low flavor thresholds. Such liners, however, are adequate for many beverage products in that their contribution of off-flavor to the beverage is not noticeable.
Some beverages, though,--notably, mineral waters--have such delicate bouquets that they cannot tolerate even the relatively slight off-flavors that can be generated with conventional liners. The polymeric cap liner of the container is a source of double-bond containing precursors that react with oxygen in bottled water. Polymeric cap liners typically contain a number of plasticizers, heat stabilizers, lubricants, antioxidants, blowing agents, and pigments, some or all of which contain double bonds that are susceptible to attack by oxygen. For example, the liner formulations for twist-off caps typically comprise oleamide-type lubricants. The double bonds in such oleamides are readily susceptible to attack by oxygen, resulting in off-flavored producing medium-chain-length aldehydes. Also, fatty acids or derivatives of fatty acids of liner compositions react with oxygen to form off-flavored aldehydes. Other compounds often found in polymeric cap liners which are susceptible to attack from oxygen include activated aromatic compounds such as phenols, and other double bond containing compounds such as ketones, amides, crucic acid, etc. The resulting aldehydes are responsible for the fruity tastes and odors often found in bottled water.
In order to produce bottled drinking water, it is necessary to disinfect the water so as to remove the microorganisms that would otherwise grow therein. In the past, water was disinfected using chlorine. However, the use of chlorine invariable resulted in the production of trihalomethanes such as chloroform which have been shown to pose a serious health risk. Alternatively, water bottling companies can use ozone as a disinfectant instead of chlorine to kill any microorganisms present in the water itself. Thus, the bottled water usually contains ozone in trace amounts. Typically, ozone is present in an amount of about 0.1 to 0.4 mg/l. These trace amounts kill the microorganisms so that is it not necessary for the water to be pasteurized. In addition, ozone oxidizes many nuisance compounds or contaminants in water supplies.
Drinking water standards in the United States specify that drinking water should not have any smell or taste. As shown by C. Anselme et al. in J. American Waterworks Association, 80, 45-51 (1988), the intensity of a fruity off-flavor correlates strongly with the total concentration of aldehydes present in the water.
Ozone also reacts with compounds which contain double bonds, such as alkenes, yielding corresponding aldehydes as the major oxidation product. As noted above, those aldehydes are responsible for the fruity tastes and odors that are found in bottled water.
While one solution to this problem is to remove the compounds that are reactive with oxygen, this solution is not practical since the liner would not possess the desired properties to properly seal the bottle. While the presence of off-flavor substances may be more readily remarked in water than in more strongly flavored beverages such as beer, the presence of such substances can adversely affect the taste of the more strongly flavored beverages. Accordingly, a need exists for an improved liner which can protect against the development of an off-flavor in bottled water or other fluids. Oxygen-related problems in beer generally
In packaging oxygen-sensitive materials such as foodstuffs, beverages, and pharmaceuticals, oxygen contamination can be particularly troublesome. Care is generally taken to minimize the introduction of oxygen or to reduce the detrimental or undesirable effects of oxygen on the product. Carbon-carbon double bonds are particularly susceptible to reaction with active oxygen species. Such carbon-carbon bonds are often found in foods and beverages, pharmaceuticals, dyes, photochemicals, adhesives, and polymer precursors. Virtually any product that has complex organic constituents will contain such carbon-carbon double bonds or other oxygen-reactive components, and hence can undergo oxidative reactions.
Where the products of the oxidative reactions adversely affect the performance, odor, or flavor of the products, then removing the oxygen which is present (either dissolved in or trapped with the product), preventing oxygen ingress, and inhibiting the reactions of oxygen will all benefit the product. A number of strategies exist to deal with oxygen as a contaminant. The most basic is simply to remove oxygen from the product by vacuum, by inert gas sparging, or both. Such systems are used in boiler water treatment, in the orange juice and brewing industries, and in modified-atmosphere packaging of food products. This technology, while somewhat equipment intensive, can remove up to 95% of the oxygen present in air from the product or its container prior to or during packaging. However, removal of the remaining oxygen using this approach requires longer times for vacuum treatment and/or sparging and increasingly larger volumes of higher and higher purity inert gas that must not itself be contaminated with trace levels of oxygen. This makes the removal of the last traces of oxygen very expensive. A further disadvantage of these methods is a tendency to remove volatile product components. This is a particular problem with foods and beverages, in which such components are often responsible for much of the aroma and flavor.
In beer, for instance, it has been known since the 1930's that oxygen in beer adversely affects it flavor and stability. Amounts of oxygen as low as 0.1 to 0.2 ml per 355 ml container will, over time, cause darkening of the beer, an increase in chill-haze values, and significant taste changes. Oxygen's effect on beer is so strongly detrimental that many brewers go to great lengths to remove it from the bottle during the filling process. One usual technique is to remove the air via vacuum from a clean bottle, fill the bottle with carbon dioxide, flow the beer down the bottle wall into the bottle thus displacing the carbon dioxide, and finally squirting a jet of high-pressure deoxygenated water into the bottle to cause the beer to over-foam just as the cap is put on, thereby attempting to displace the remaining headspace gases with the beer's own carbon dioxide. In addition, production lines are run slowly in order to minimize the introduction of air into the headspace just before capping. All of this is expensive, and usually reduces the total oxygen concentration in the headspace to about 200-400 parts per billion. The 200-400 ppb achieved in the packaged product by careful brewers corresponds to approximately 50-100 microliters of oxygen per 355 ml bottle. Even this small quantity of oxygen is still considered to be one of the major limitations on quality and shelf life of beer today. The desired level is as close to zero as possible, but certainly below about 50 ppb.
Prior art oxygen scavenging
None of the above techniques remove or control oxygen that is dissolved in the product or leaked or permeated into the package. Compounds such as sulfur dioxide, trihydroxybutyrophenone, butylated hydroxy toluene, butylated hydroxy anisole, ascorbic acid, isoascorbic acid, and glucose oxidase-catalase have been used in an attempt to reduce the effects of oxygen when it is dissolved in beer. See, for instance, Reinke et al., "Effect of Antioxidants and Oxygen Scavengers on the Shelf-Life of Canned Beer", A.S.B.C. Proceedings, 1963, pp. 175-180; Thomson, "Practical Control of Air in Beer", Brewer's Guild Journal, Vol. 38, No. 451, May 1952, pp. 167-184; von Hodenberg, "Removal of Oxygen from Brewing Liquor", Brauwelt International, III, 1988, pp. 243-4.
The direct addition of such agents into beer has several disadvantages. Both sulfur dioxide and ascorbates, when added to beer, can result in production of off-flavors, thus negating the intended purpose of the addition. Many studies have been conducted on the effect of such agents on the flavor of beer. See, for instance, Klimowitz et al., "The Impact of Various Antioxidants of Flavor Stability", MBAA Technical Quarterly, Vol. 26, 1989, pp. 70-74; Gray et al., "Systematic Study of the Influence of Oxidation on Beer Flavor", A.S.B.C. Proceedings, 1948, pp. 101-112, Also, direct addition of such compounds to a food or beverage requires stating on the label that the product contains the additive--an undesirable matter with today's emphasis on "freshness" and "all natural" products.
Attempts have been made to incorporate oxygen scavenging systems in a container crown or closure. For instance, U.S. Pat. No. 4,279,350 discloses a closure liner that incorporates a catalyst disposed between an oxygen-permeable barrier and a water-absorbent backing layer. U.K. Patent Application No. 2,040,889 discloses a closure in the form of a stopper molded from ethylene vinyl acetate ("EVA") having a closed-cell foamed core that may contain water and sulfur dioxide to act as an oxygen scavenger and a liquid-impervious skin. European Patent Applications Nos. 328,336 and 328,337 disclose container closure elements, such as caps, removable panels, liners, or sealing compositions that are formed of a polymeric matrix containing an oxygen scavenger therein. U.S. Pat. No. 4,287,995 discloses a sealing member for a container that is used to preserve aqueous liquids therein. This sealing member is mounted on the cap or stopper of the container on the portion facing the contents. The sealing member contains an oxygen absorbent that is separated from contacting the contents of the container by a film that has a plurality of fine openings such that it is gas-permeable but water-impermeable at one atmosphere pressure.
U.S. Pat. No. 5,143,763 describes an approach that prevents oxygen deterioration in containerized substances that relies on the absorption of oxygen from within the container. This patent does not teach how to prevent the containerized substances from developing off flavor that is due to leaching substances from the liner.
The present invention protects containerized beverages such as beer and water from developing off-flavor due to leaching of aldehydes from the crown liner. This invention is directed to a liner composition for a closure element of a container for potable fluids such as water. The liner composition includes at least an inorganic sulfite compound or a tocopherol compound in amount sufficient to protect against the development of off-flavor in a potable fluid in the container. The preferred inorganic sulfite compound is a sulfite salt such as sodium sulfite. The preferred tocopherol compound is dl-α-tocopherol.
The invention is also directed to a potable fluid container comprising a reservoir element for containing fluid, which element has an opening, a closure element capable of being attached to the opening, and the above-described liner composition associated with the closure element. Generally, the closure has a recessed portion for receiving the container opening, and the liner is placed within the recess of the closure element between the container opening and the closure element for sealing the fluid within the container.
Another aspect of the invention relates to a method of improving the taste of a bottled fluid such as water by containing the fluid in the above potable fluid container and associating the above liner composition with the container so that the inorganic sulfite compound or tocopherol compound can react with residual oxygen in the headspace.
Still another aspect of the present invention is a method of making a liner composition for a potable-fluid-container closure element that comprises combining a thermoplastic polymer with a first flavor protectant compound of an inorganic sulfite compound or a tocopherol compound in an amount sufficient to prevent or inhibit the formation in the liner composition of off-flavor-causing substances and subsequently shaping a portion of said thermoplastic polymer into a shape that will enable it to function as a liner for a closure element and affixing said shaped thermoplastic polymer into place in or on said closure element.
This invention relates in part to container closures for use in combination with means for retaining a water-containing foodstuff, beverage, chemical, or pharmaceutical product, which retaining means has a least one opening therein for filling or dispensing of the product. These container closures include a member for closing the opening of the retaining means and preventing escape of the liquid product when not desired, and a liner or gasket comprising one of the flavor protectant compositions described above being positioned adjacent the closing member. Preferably, the retaining means is a can, jar, or bottle of metal, glass, or plastic construction, and the closing member is a crown or closure.
The polymers
A wide variety of polymers may be used in accordance with the teaching of the present invention. For use in applications such as crown or closure liners, the polymer is preferably a polymeric thermoplastic, such as PVC, EVA, polyethylene terephthalate ("PET"), PE, or polypropylene ("PP"), or a polyurethane. U.S. Pat. No. 3,547,746 provides much useful disclosure about these and thus is expressly incorporated herein by reference. The PVC resins that are preferred for use as the polymer in the flavor protectant compositions of the invention are set forth in the patent at column 2, lines 35-47. This patent also discloses suitable plasticizer compounds that may be used with the thermoplastic resin along with preferred ranges thereof. In this invention, it is preferred to use an amount of plasticizer ranging from about 60 to 90 parts by weight based on 100 parts by weight of the polymer for crown liners. Depending upon the specific product to be made, the amount of plasticizer can vary from 10 to 120 parts. Specific plasticizers for PVC crown liners are recited in column 5, lines 49-53 of the patent.
The polymer should have a rate of water vapor transmission of between 0.05 and 25 g-mm/m2 /24 hours at 37.8° C. PVC typically provides a value of 2-12, PE between 0.1 and 1, and EVA 0.8 to 1.2. These rates are sufficient to enable the water vapor to permeate the polymer to activate the flavor protectant materials therein. The polymer should also be permeable to oxygen and have a permeability rate of between 50 and 2000, and preferably between 100 and 1500 cc-mil/100 square inches/24 hours per atmosphere pressure at 25° C. PVC provides values between 100-1400, PE about 185-500, and EVA about 830-850.
The flavor protectant agents
In the present invention, the liner composition comprises a first flavor protectant agent that is either an inorganic sulfite compound or a tocopherol compound in an amount sufficient to protect against the development of off-flavor in a potable fluid in the container. The inorganic sulfite compound may be an alkaline earth metal sulfite or an alkali metal sulfite. The alkali metal salts such as sodium sulfite are preferred. As indicated in Kirk-Othmer, Encyclopedia of Chemical Technology, 3rd Ed., Vol. 22, pp. 149-151 (1983), sodium sulfite is a well-known and versatile chemical. Its use pattern is 60% in sulfite pulping, 15% in water treatment (dechlorination, deoxygenation), 12% in photography, and 13% in miscellaneous uses. Various applications of sulfites are described in U.S. Pat. Nos. 2,825,651, 4.041,209, 4,113,652, 4,287,995, 4,536,409, 4,702,966, 5,075,362, 5,106,886, 5,204,389, and 5,227,411. However, none of these involves the use of sulfites in liner formulations to protect the flavor of containerized beverages.
A wide variety of tocopherol compounds can be used. The compound dl-α-tocopherol, also known as vitamin E, is structurally identified as 2,5,7,8-tetramethyl-2-(4',8',12'-trimethyltridecyl)-6-chromanol. While dl-α-tocopherol, or vitamin E, is currently the preferred tocopherol compound, other tocopherol compounds, including not only the stereospecific isomers of α-tocopherol but also β-tocopherol, i.e., 2,5,8-trimethyl-2-(4',8',12'-trimethyltridecyl)-6-chromanol, γ-tocopherol, i.e., 2,7,8-trimethyl-2-(4',8',12'-trimethyltridecyl)-6-chromanol, and δ-tocopherol, i.e., 2,8-dimethyl-2-(4',8',12'-trimethyltridecyl)-6-chromanol may also be used in accordance with the present invention. In addition to its use as a dietary supplement, dl-α-tocopherol is marketed, for instance by Roche under the name RONOTEC 201, as an antioxidant in polymers and oils. However, there has been no suggestion that dl-α-tocopherol could be used in liner formulations to protect the flavor of containerized beverages.
The only restrictions on the inorganic sulfite compounds and tocopherol compounds for use in the liners of the present invention are that they should be compatible with the material and other components of the liner and approved by the FDA for use in contact with the fluid to be ingested. Preferably, the inorganic sulfite compound is present in the liner composition in an amount of from about 0.3 to about 5%, and more preferably 0.5 to 3%, by weight of the composition, while the tocopherol compound is present in the liner composition in an amount of from about 0.3 to about 3%, and more preferably 0.5 to 1%, by weight of the composition.
The liner composition is generally made of a material which is permeable to gases and water or water vapor. As noted above, this material would typically be a polymer, such as a thermoplastic resin. Thermoplastic resins of polyolefins such as PE and the like, PVC, EVA, and the like would allow gases such as oxygen or ozone, and water or water vapor to pass into and through the liner. The inorganic sulfite or tocopherol of the present invention protects against the development of off-flavors which would otherwise result from the formation of aldehydes due to the reaction of oxygen sources present in the potable fluid with prior art liner compositions or components thereof.
While it is contemplated in accordance with the present invention to use a single flavor protectant compound, it is often preferable to use a combination of flavor protectant compounds. The most preferred combination would be a sulfite compound and a tocopherol compound. However, additional flavor protectant compounds can often advantageously be used along with the inorganic sulfites or tocopherols according to the present invention, however. Generally, the second flavor protectant compound can be used in an amount of between about 0.1 and 5% by weight. Typical examples of such additional compounds include 1 to 2% by weight of an ascorbate such as sodium ascorbate and 1 to 3% by weight of a hydrazide compound. The preferred hydrazide is a sulfonyl hydrazide such as OBSH or p-toluene sulfonyl hydrazide. Carboxylic acid hydrazides can also be used. The use of hydrazides is disclosed in commonly assigned application Ser. No. 08/167,257, the content of which is expressly incorporated herein by reference thereto. The use of ascorbates such as vitamin C and related compounds (e.g., sodium ascorbate) is disclosed in U.S. Pat. No. 5,202,052, the content of which is also expressly incorporated herein by reference thereto.
In the present invention, the hydrazide compound is an "unactivated hydrazide," i.e., a hydrazide compound which has not been subjected to a decomposition reaction. This can occur by either adding an amount of a hydrazide compound beyond that which is needed for use as a blowing agent or by processing the liner so as to not decompose the hydrazide compound which is present.
Hydrazides of organic sulfonic acids have been found to be useful in the present invention. Both aliphatic and aromatic sulfonic acids can be used, with one or both --NH2 groups of the hydrazine molecule being substituted with alkyl or aryl radicals. The most preferred compound is a sulfonyl hydrazide, such as OBSH, since it has FDA approval for applications and articles which come into contact with food or beverages. Other sulfonyl hydrazides such s p-toluene sulfonyl hydrazide can be used, if desired. Thus, the useful hydrogens may optionally be substituted by other organic moieties.
Other hydrazides which may be used to reduce the off-flavor of bottled water include carboxylic acid hydrazides of the general structure shown below. ##STR1## where R is hydrogen, a straight chain or branched alkyl or alkenyl group of 1 to 20 carbon atoms, a phenyl group, which is substituted or unsubstituted, or the like.
The only restrictions on the hydrazide compounds for use in the liners of the present invention are that the hydrazide compound be compatible with the material and other components of the liner and that the compound be FDA approved for use in contact with the fluid to be ingested. Preferably, the hydrazide compound may be present in the liner composition in an amount of from about 0.1 to about 1% by weight of the composition.
Since the liner composition may also include a hydrazide compound for use as a blowing agent, the composition must be formulated so that the amount of hydrazide compound that is decomposed is less than the total amount of hydrazide compound that is added to the liner composition. This decomposition may be activated by an activator or by heat. In the present invention, an activator for decomposing the hydrazide compound is added in an amount that is less than that necessary to activate the total amount of hydrazide compound in the liner composition. Examples of typical activators include carbonates, glycols, ureas, acids, alkanolamines, oxidizing agents such as peroxides. In particular, carbonates such as sodium carbonate are preferred activators. The present invention may also include at least one blowing agent other than the unactivated hydrazide compound, if desired.
Manufacture
Preferred uses of the compositions of the invention are as liners or gaskets in crowns or closures for capping beverage bottles. Entire closures may also be made of plastics containing compositions of the invention, for instance all plastic screw-on threaded caps for soft drink bottles, and the like. Another preferred use of the composition of the invention is as a gasket or liner applied to an aluminum or plastic closure or metal crown for plastic or glass bottles.
Conventional bottle closure linings are made of a thermoplastic material, such as PVC or EVA, polyolefins such as PE or PP, or blends thereof. In order to attain the optimum combination of moldability, resilience, sealability, etc., these materials are formulated to include plasticizers, heat stabilizers, lubricants, blowing agents, antioxidants, pigments, and other additives. These additive components are well known to one skilled in the art so that a detailed description is not needed herein.
As noted above, PVC liners are well known for use in crowns as described in the production of crowns using the Za-Matic machines. There is also well know technology for making aluminum or plastic closures containing EVA liners. The disclosure of U.S. Pat. No. 3,547,746 is likewise useful for its teachings of crown liner manufacturing techniques, and thus is expressly incorporated herein by reference thereto on this point as well. In addition to this crown liner manufacturing method, which is generally used for PVC, EVA, or PE liners, many other devices can apply liners by plastisol spin-lining or various hot molding techniques. The present invention is easily applicable to both gasketing/coating/sealing materials for metal crowns or closures, such as beer bottle crown or soda closure liners, and to containers or closures comprised primarily of plastic materials.
Formulations according to the present invention may be prepared for use in a Za-Matic machine for application as a liner to a beer bottle crown. The PVC resin is placed in a dry mix kettle, and plasticizer is added with continuous heating and mixing. All other additives, including the flavor protectant material, are then gradually introduced into the resin to form a dry blend. This dry blend is place into an extruder and pelletized to form the liner compound that is added to the Za-Matic machine to form liners on metal bottle crowns.
U.S. Pat. No. 5,202,052 describes this and other liner manufacturing procedures that may be adapted by those skilled in the art to manufacture the liners of the present invention. The inorganic sulfite compound or tocopherol compound may be admixed into the liner or can be coated thereon or otherwise associated therewith.
Preferably, the potable fluid container of the present invention contains a potable fluid, most preferably beer or water. Preferably, the potable fluid container has ozone added thereto. In the case of water, the ozone is preferably added in trace amounts, such as from about 0.1 to 0.5 mg/l.
The foregoing and other objects, features, aspects, and advantages of the present invention will become more apparent from the following detailed nonlimiting examples of the present invention.
In order to demonstrate that the addition of inorganic sulfite compositions and tocopherol compositions in accordance with the present invention permits the formulation of liners that impart less off-flavor to beverages, test samples were prepared and compared to controls. It is emphasized that the taste of the water, even though it has important commercial consequences, may be regarded as an indicator of the presence in the liners of extractable off-flavor-causing substances.
A fresh control was prepared for each experiment. A panel of trained flavor tasters evaluated the samples along with an outside consultant. The liner materials were evaluated for improved flavor over the control after one day and long term storage.
In each example, twelve-ounce flint glass bottles were filled with 350.0±0.5 ml. of artesian spring water. Into each bottle for each test cell were placed four bottle cap liners made of the lining material of interest, formulated as in Table 1, and the bottle was crowned with the closure that was lined with the same material that was placed inside the bottle. Since each of the four liners placed inside of the bottle presented both sides to the liquid, with the liner used in the cap the effective number of liners contributing to the concentration of materials of interest in each cell was nine times that which would be achieved with a lined cap alone.
The bottles were pasteurized at 140° F. for 20 minutes, cooled to 90° F., and stored at room temperature for various periods of time, up to sixteen days. After the storage period, the water was evaluated by the flavor panel for any off-flavors. The intensity of the off-flavor was scored by each panelist on a scale of 0 (No detectable off-flavor) to 3 (intense off-flavor). The individual panelists scores were averaged to determine the panel's overall score for each product. The control was prepared in the same manner as the test samples.
The effect of combination of sodium sulfite and dl-α-tocopherol in closure liners was evaluated in this Example. The results of the flavor evaluations are shown in Table 1.
TABLE 1
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Control
1 2 3 4
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FORMULATIONS:
PVC Resin 200.00 200.00 200.00 200.00
200.00
Plasticizer
120.00 120.00 120.00 120.00
120.00
Stabilizer 2.00 2.00 2.00 2.00 2.00
Lubricant 4.00 4.00 4.00 4.00 4.00
Silica Pigment
0.61 0.61 0.61 0.61 0.61
Sodium Sulfite
0.00 1.65 1.65 3.30 3.30
dl-α-Tocopherol
0.00 1.65 3.30 1.65 3.30
totals 326.61 329.91 331.56 331.56
333.21
Flavor Intensity Ratings
EVALUATIONS:
(Scale 0-3)
1 Day 1.95 2.3 1.2 1.7 2.5
5 Days 2.0 0.5 -- -- 0.0
14 Days 2.0 -- 0.5 0.0 --
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The results reported in Table 1 indicate that liner formulations containing a combination of inorganic sulfite compound and tocopherol in accordance with the present invention generally exhibit significantly less flavor contamination over time than do similar formulations that do not contain the inorganic sulfite and tocopherol combination. Thus it is apparent that the incorporation of said combination into the liner composition has forestalled the formation of extractable off-flavor-causing substances in said liner composition.
The effect of a combination of sodium sulfite and a hydrazide--specifically OBSH--in closure liners was evaluated in this Example. The results of the flavor evaluations are shown in Table 2.
TABLE 2
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Control 5 6
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FORMULATIONS:
PVC Resin 200.00 200.00 200.00
Plasticizer 120.00 120.00 120.00
Stabilizer 2.00 2.00 2.00
Lubricant 4.00 4.00 4.00
Silica Pigment
0.61 0.61 0.61
Sodium Sulfite
0.00 1.65 3.30
OBSII 0.00 0.65 0.65
totals 326.61 328.91 330.56
Flavor Intensity Ratings
EVALUATIONS: (Scale 0-3)
5 Days 1.5 0.4 0.3
14 Days 0.5 0.0 0.0
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The results reported in Table 2 indicate that liner formulations containing an inorganic sulfite compound in combination with OBSH result in the least flavor contamination than do similar formulations which do not contain the inorganic sulfite and OBSH components. Thus it is apparent that the incorporation of said combination into the liner composition has forestalled the formation of extractable off-flavor-causing substances in said liner composition.
The effect of a combination of dl-α-tocopherol and OBSH on closure liners was evaluated in this Example. The results of the flavor evaluations are reported in Table 3.
TABLE 5
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Control 7 8
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FORMULATIONS:
PVC Resin 200.00 200.00 200.00
Plasticizer 120.00 120.00 120.00
Stabilizer 2.00 2.00 2.00
Lubricant 4.00 4.00 4.00
Silica Pigment
0.61 0.61 0.61
dl-α-Tocopherol
0.00 1.65 3.30
OBSII 0.00 0.65 0.65
totals 326.61 328.91 330.56
Flavor Intensity Ratings
EVALUATIONS: (Scale 0-3)
2 Days 2.3 -- 0.6
5 Days 1.5 6.2 --
14 Days 1.5 1.0 1.0
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The results reported in Table 3 indicate that liner formulations containing a combination of dl-α-tocopherol and OBSH in accordance with the present invention result in less flavor contamination than do similar formulations which do not contain the dl-α-tocopherol and OBSH components. Thus it is apparent that the incorporation of said combination into the liner composition has forestalled the formation of extractable off-flavor-causing substances in said liner composition.
The effect of a combination of sodium sulfite and sodium ascorbate on closure liners was evaluated in this Example. The results of the flavor evaluations are shown in Table 4.
TABLE 4
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Control
9 10 11
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FORMULATIONS:
PVC Resin 200.00 200.00 200.00
200.00
Plasticizer 120.00 120.00 120.00
120.00
Stabilizer 2.00 2.00 2.00 2.00
Lubricant 4.00 4.00 4.00 4.00
Silica Pigment
0.61 0.61 0.61 0.61
Sodium Sulfite
0.00 1.65 3.30 10.00
Sodium Ascrobate
0.00 5.40 6.40 4.00
totals 326.61 334.66 336.31
340.61
Flavor Intensity Ratings
EVALUATIONS: (Scale 0-3)
1 Day 2.55 2.6 2.8 1.1
5 Days 2.0 0.5 0.5
16 Days 3.0 -- -- 0.5
______________________________________
The results reported in Table 4 indicate that liner formulations containing an inorganic sulfite compound in combination with sodium ascorbate in accordance with the present invention vary over time in their effect on flavor contamination as compared to similar formulations which do not contain the inorganic sulfite and ascorbic acid components. It appears that the addition of ascorbic acid as an ascorbate enhances the effectiveness of the sulfite, particularly over longer periods of storage. Thus it is apparent that the incorporation of said combination into the liner composition has forestalled the formation of extractable off-flavor-causing substances in said liner composition.
The effect of a combination of dl-α-tocopherol and sodium ascorbate on closure liners was evaluated in this Example. The results of the flavor evaluations are shown in Table 5.
TABLE 5
______________________________________
Control 12 13
______________________________________
FORMULATIONS:
PVC Resin 200.00 200.00 200.00
Plasticizer 120.00 120.00 120.00
Stabilizer 2.00 2.00 2.00
Lubricant 4.00 4.00 4.00
Silica Pigment
0.61 0.61 0.61
dl-α-Tocopherol
0.00 1.65 3.30
Sodium Ascorbate
0.00 0.40 0.40
totals 326.61 334.66 336.31
Flavor Intensity Ratings
EVALUATIONS: (Scale 0-3)
1 Day 1.6 1.8 2.4
14 Days 2.0 3.0 1.5
______________________________________
The results reported in Table 5 indicate that liner formulations containing dl-α-tocopherol in combination with sodium ascorbate in accordance with the present invention vary over time in their effect on flavor contamination as compared to similar formulations which do not contain the dl-α-tocopherol and ascorbic acid components. The best results are obtained with the higher concentrations of the tocopherol compound. Thus it is apparent that the incorporation of said combination into the liner composition has forestalled the formation of extractable off-flavor-causing substances in said liner composition.
The addition of different amounts of sodium sulfite to the bottle crown liner described hereinabove was investigated. The results of the flavor evaluations are shown in Table 6.
TABLE 6
______________________________________
Control 14 15
______________________________________
FORMULATIONS:
PVC Resin 200.00 200.00 200.00
Plasticizer 120.00 120.00 120.00
Stabilizer 2.00 2.00 2.00
Lubricant 4.00 4.00 4.00
Silica Pigment
0.61 0.61 0.61
Sodium Sulfite
10.00 1.65 3.30
totals 326.61 332.26 329.91
Flavor Intensity Ratings
EVALUATIONS: (Scale 0-3)
1 Day 2.8 2.4 2.2
16 Days 3.0 2.0 1.0
______________________________________
The results reported in Table 6 indicate that liner formulations containing an inorganic sulfite compound in accordance with the present invention result in less flavor contamination than do similar formulations which do not contain the inorganic sulfite compound, with the degree of improvement increasing with increasing amounts of sodium sulfite. Thus it is apparent that the incorporation of said combination into the liner composition has forestalled the formation of extractable off-flavor-causing substances in said liner composition.
The addition of different amounts of dl-α-tocopherol to the bottle crown liner described above was investigated. The results of the flavor evaluations are shown in Table 7.
TABLE 7
______________________________________
Control 16 17
______________________________________
FORMULATIONS:
PVC Resin 200.00 200.00 200.00
Plasticizer 120.00 120.00 120.00
Stabilizer 2.00 2.00 2.00
Lubricant 4.00 4.00 4.00
Silica Pigment
0.61 0.61 0.61
dl-α-Tocopherol
0.00 1.65 3.30
totals 326.61 328.26 329.91
Flavor Intensity Ratings
EVALUATIONS: (Scale 0-3)
2 Days 2.3 1.6 1.4
14 Days 2.5 1.0 1.0
______________________________________
The results reported in Table 1 indicate that liner formulations containing dl-α-tocopherol in accordance with the present invention result in less flavor contamination than do similar formulations which do not contain the dl-α-tocopherol. Thus it is apparent that the incorporation of said combination into the liner composition has forestalled the formation of extractable off-flavor-causing substances in said liner composition.
Seven 200 ml water samples were each ozonized as follows. Seven samples of 206±0.5 grams of distilled water were each poured into a clean 7 ounce bottle. A Sander Ozonizer Model 25, having 25 mg per hour capacity was connected to a 100% oxygen tank via a silicone rubber tubing. The outlet of the ozonizer was connected to Teflon tubing via silicon rubber tubing to minimize the exposure of the silicon rubber to the ozone. The Teflon Tubing was connected to a glass gas dispersion tube, Catalog Number 9435A of Ace Glass, Inc., Vineland, N.J., via silicone rubber tubing. The glass gas dispersion rube was immersed in water. The ozone concentration was controlled with oxygen flow and flow time. An oxygen flow 115-121 ml with 25 mg per hour setting of ozonizer resulted in 0.4 to 0.5 mg/l (ppm) of ozone in the 7 ounce bottle of water after 3.5 minutes. The concentration of ozone was determined with an Ozone Test Kit, Hack Chemical Co. Model OZ-2, Catalog No. 20644-00, Loveland, Colo. The analytical range of ozone detection is 0.1-2.3 mg/l.
To determine whether the components of the liner are the source of off-flavor in the water samples, the components are separately added to the samples, each in an amount of 2 mg. The composition of the liner is given below in Table 8.
TABLE 8
______________________________________
Parts
Component (lbs)
______________________________________
PVC Resin 200
Primary Plasticizer
153
Secondary Plasticizer A
11.8
Stabilizer 2
Lubricant Package 3.37
______________________________________
Specifically, 2 mg of each one of OBSH, the primary plasticizer, the secondary plasticizer and the three components of the lubricant package are separately added to six samples, respectively. Lubricant #1 and lubricant #2 are amides of an unsaturated fatty acid, and lubricant #3 is a paraffin wax. A seventh sample was used as a control, having nothing added thereto. The bottles were immediately crowned and later tested for flavor.
The final ozone concentration before crowning was determined to be 0.4 to 0.5 mg/l. The bottles were stored at room temperature for two days. Calorimetric analysis showed that the control sometimes contained unreacted ozone after two days, while no ozone remained in any of the bottles to which the additional components had been added.
The samples were then evaluated by a taste panel, evaluating the off-flavor intensity of the samples. The results were such that the sample containing OBSH and the control had approximately the same flavor, which flavor was less than for the samples containing the secondary plasticizer and the lubricants, with the sample containing lubricant #2 having the strongest flavor of all the samples evaluated.
Three samples of distilled water were bubbled with ozone as in Example 18 to contain a concentration of 0.4-0.5 mg/l ozone and then were crowned in a bottle with the following liners having the following formulations:
TABLE 9
______________________________________
LINER FORMULATION
Component 18 19 20
______________________________________
PVC Resin 200 200 200
Prim. Plast. 144 153 153
Sec. Plast. A
13.2 11.8 --
Stabilizer -- 2 0.74
Anti-Oxidant 1.6 -- --
OBSII 1.4 -- --
Sec. Plast. B
-- -- 11.8
Lubricant Package
9.0 3.37 5.0
Pigment -- -- 0.16
Drying agent 0.67 -- --
______________________________________
The bottles were stored at 22° C. for four days and then tasted by a taste panel for evaluating the off-flavor intensity of the samples. The results were that liner 18 had no off-flavor, liner 19 had a very weak off-flavor and liner 20 had a strong off-flavor. The superiority of liner 18, despite its lubricant package, is attributed to the presence of OBSH.
In order to evaluate the effect of increasing temperature and time of storage, 3 bottles of distilled water were ozonized as in Example 18 and were crowned with liners 19, 19+(0.2% OBSH) and 20.
The bottles were stored for 56 days at 30° C. and were evaluated for off-flavor by a taste panel. The results were as follows:
TABLE 10
______________________________________
OFF-Flavor Intensity
LINER (0-3 Scale)
______________________________________
19 2
19 + (0% OBSII)
1
20 3
______________________________________
The OBSH containing sample was found to be clearly superior to the other samples.
Three bottles of distilled water were ozonized as in Example 18 to contain 0.4 mg/l ozone. The bottles were capped with the following closure tapes which were made from a copolymer of ethylene vinyl acetate comprising of 10% vinyl acetate having the following formulations:
TABLE 11 ______________________________________ CLOSURE TAPE FORMULATIONS Component CT-1 CT-2 CT-3 ______________________________________ Virgin 60% 100% 100% Regrind EVA 40% -- -- OBSII -- -- 0.2 ______________________________________
After storage for four days at room temperature, taste tests found that CT-1 had weak off-flavor intensity, CT-2 had moderate off-flavor intensity, and CT-3 had no off-flavor intensity.
Six bottles of water were ozonized as in Example 18 to contain a concentration of 0.4-0.5 mg/l ozone. The bottles were sealed with crown liner elements 18, 19, 19+(0.2% OBSH) and with closure tapes CT-1, CT-2, and CT-3. The bottles were then heated at 30° C. for 30 days. A taste panel then evaluated that taste of each sample for off-flavor intensity on a scale of 0-3, with 0 having no off-flavor and 3 having an intense off-flavor. The results are as follows.
TABLE 12
______________________________________
CLOSURE ELEMENT
OFF-FLAVOR INTENSITY
______________________________________
18 2.0
19 2.4
19 + (0.2% OBSII)
1.7
CT-1 2.0
CT-2 1.6
CT-3 0.6
______________________________________
The intensity of off-flavors of the closure tapes increased for each sample when compared to the four day, room temperature test examples. However, some protective effect of OBSH was still evident.
Three bottles of water were ozonized as in Example 18 to maintain a concentration of 0.4 mg/l of ozone. The bottles were sealed with the following crown liner elements.
TABLE 13
______________________________________
FORMULATION
Component 21 22 23
______________________________________
PVC RESIN 200 200 200
PRIMARY PLASTICIZER
153 153 153
SECONDARY PLASTICIZER A
11.8 11.8 11.8
STABILIZER 2 2 2
OBSII -- -- 0.7
LUBRICANT PACKAGE
3.37 1.28 3.37
______________________________________
These three bottles were evaluated for off-flavor intensity after storage for 4 days at room temperature. The taste of the formulation having the OBSH was found to be the cleanest, while the other formulations were found to have oxidized, aldehyde flavors.
4 bottles of distilled water were ozonized as in Example 1 and were crowned with the following liners having the following compositions.
TABLE 14
______________________________________
LINER FORMULATION
Component 24 25
______________________________________
PVC RESIN 200 200
PRIMARY PLASTICIZER 164.8 164.8
SECONDARY PLASTICIZER A
-- --
STABILIZER 2 2
OBSII -- 1.85
LUBRICANT PACKAGE 3.37 3.37
______________________________________
The bottles were stored for 5 days at room temperature and were evaluated for off-flavor by a taste panel. The results, based on a scale of 0-3, were as follows.
TABLE 15 ______________________________________ LINER OFF-FLAVOR INTENSITY ______________________________________ 24 21.5 25 0.3 ______________________________________
Formulation 25, containing 0.5% OBSH based on the total weight of the liner formulation, was unanimously rated the best by the panel.
Although the present invention has been described in detail, it is clearly understood that the same is by way of example only and is not to be taken by way of limitation, the scope of the present invention being limited only by the terms of the appended claims.
Claims (13)
1. A closure element for a bottles fluid, which element includes a liner composition consisting essentially of a polymer, a hydrazide compound present in a non-decomposed state and in an amount sufficient to at least partially inhibit the formation of off-flavor causing substances in the liner composition, and a further, different flavor protectant compound in an amount which, in combination with the amount of hydrazide compound, prevents or inhibits the formation of off-flavor causing substances in the liner composition, thus improving the taste of the bottled fluid compared to bottled fluids which include closure elements having liner compositions that do not include the hydrazide and further flavor protectant compounds in said amounts.
2. The liner composition of claim 1 wherein the hydrazide composition is 4,4'-oxybis(benzene sulfonyl hydrazide) and is present in an amount of between about 0.1 and 5% as weight of the liner composition.
3. The liner composition of claim 1 wherein the hydrazide compound is a sulfonyl hydrazide and the further flavor protectant compound is an inorganic sulfite compound or a tocopherol compound, said further flavor protectant compound being present in an amount of from about 0.3 to about 5% by weight of the liner composition.
4. The liner composition of claim 1 wherein the polymer is a thermoplastic resin compound selected from the group consisting of a polyolefin, polyvinyl chloride, ethylene-vinyl acetate of a mixture thereof.
5. The liner composition of claim 1 further consisting essentially of one or more of a plasticizer, a heat stabilizer, a lubricant, a blowing agent or a pigment, and the bottled fluid is beer or water.
6. A method of improving the taste of a fluid which is retained in a bottle by a closure element that includes a liner composition as a seal, which method comprises providing, in the liner composition during manufacture thereof, two different flavor protectant compounds in amounts which, in combination, are sufficient to prevent or inhibit the formation in the liner composition of off-flavor causing substances, wherein at least one compound is a hydrazide compound in a non-decomposed state, thus improving the taste of the fluid compared to bottled fluids which are retained by closure elements having liner compositions that do not include the different flavor protectant compounds in said amounts.
7. The method of claim 6 wherein the hydrazide compound is present in an amount of about 0.1 and 5% by weight of the liner composition.
8. The method of claim 7 wherein the hydrazide compound is a sulfonyl hydrazide and the other flavor protectant compound is an inorganic sulfite compound or a tocopherol compound.
9. The method of claim 8 wherein the other flavor protectant compound is present in an amount of from about 0.3 to about 5% by weight of the liner composition.
10. The method of claim 6 wherein the polymer is a thermoplastic resin compound selected from the group consisting of a polyolefin, polyvinyl chloride, ethylene-vinyl acetate or a mixture thereof.
11. The method of claim 6 which further comprises adding to the liner composition during manufacture thereof, one or more of a plasticizer, a heat stabilizer, a lubricant, a blowing agent or a pigment, and the fluid is beer or water. .Iadd.
12. A closure element for a bottled fluid, which element includes a liner composition consisting essentially of a polymer, a hydrazide compound present in a non-decomposed state and in an amount sufficient to at least partially inhibit the formation of off-flavor causing substances in the liner composition, thus improving the taste of the bottled fluid compared to bottled fluids which include closure elements having liner compositions that do not include the non-decomposed hydrazide therein..Iaddend..Iadd.13. The liner composition of claim 12 wherein the hydrazide compound is a sulfonyl hydrazide..Iaddend..Iadd.14. The liner composition of claim 12 wherein the hydrazide compound is 4,4'-oxybis (benzene sulfonyl hydrazide) ..Iaddend..Iadd.15. The liner composition of claim 14, wherein the 4,4'-oxybis (benzene sulfonyl hydrazide) is present in an amount of between about 0.1 and 1% as weight of the liner
composition..Iaddend..Iadd.16. The liner composition of claim 12 wherein the polymer is a thermoplastic resin compound selected from the group consisting of a polyolefin, polyvinyl chloride, ethylene-vinyl acetate or a mixture thereof..Iaddend..Iadd.17. The liner composition of claim 12 further consisting essentially of one or more of a plasticizer, a heat stabilizer, a lubricant, a blowing agent or a pigment, and the bottled fluid is beer or water..Iaddend..Iadd.18. A method of improving the taste of a fluid which is retained in a bottle by a closure element that includes a liner composition as a seal, which method comprises providing, in the liner composition during manufacture thereof, at least one flavor protectant compound in an amount which is sufficient to prevent or inhibit the formation in the liner composition of off-flavor causing substances, wherein the at least one compound is a hydrazide compound in a non-decomposed state, thus improving the taste of the fluid compared to bottled fluids which are retained by closure elements having liner compositions that do not include the flavor protectant compound therein..Iaddend..Iadd.19. The method of claim 18 wherein the hydrazide compound is present in an amount of about 0.1 to 1% by weight of the liner composition..Iaddend..Iadd.20. The method of claim 18 wherein the hydrazide compound is a sulfonyl hydrazide..Iaddend..Iadd.21. The method of claim 18 wherein the hydrazide compound is 4,4'-oxybis (benzene sulfonyl hydrazide)..Iaddend..Iadd.22. The method of claim 18 wherein the polymer is a thermoplastic resin compound selected from the group consisting of a polyolefin, polyvinyl chloride, ethylene-vinyl acetate of a mixture thereof..Iaddend..Iadd.23. The method of claim 18 which further comprises adding to the liner composition during manufacture thereof, one or more of a plasticizer, a heat stabilizer, a lubricant, a blowing agent or a pigment, and the fluid is beer or water..Iaddend.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US09/398,935 USRE36815E (en) | 1994-08-11 | 1999-09-16 | Flavor protectant closure liner compositions |
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US08/289,170 US5663223A (en) | 1994-08-11 | 1994-08-11 | Flavor protectant closure liner compositions |
| US08/908,577 US5863964A (en) | 1994-08-11 | 1997-08-08 | Flavor protectant closure liner compositions |
| US09/398,935 USRE36815E (en) | 1994-08-11 | 1999-09-16 | Flavor protectant closure liner compositions |
Related Parent Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US08/289,170 Continuation US5663223A (en) | 1994-08-11 | 1994-08-11 | Flavor protectant closure liner compositions |
| US08/908,577 Reissue US5863964A (en) | 1994-08-11 | 1997-08-08 | Flavor protectant closure liner compositions |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| USRE36815E true USRE36815E (en) | 2000-08-08 |
Family
ID=23110351
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US08/289,170 Expired - Fee Related US5663223A (en) | 1994-08-11 | 1994-08-11 | Flavor protectant closure liner compositions |
| US08/908,577 Ceased US5863964A (en) | 1994-08-11 | 1997-08-08 | Flavor protectant closure liner compositions |
| US09/398,935 Expired - Fee Related USRE36815E (en) | 1994-08-11 | 1999-09-16 | Flavor protectant closure liner compositions |
Family Applications Before (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US08/289,170 Expired - Fee Related US5663223A (en) | 1994-08-11 | 1994-08-11 | Flavor protectant closure liner compositions |
| US08/908,577 Ceased US5863964A (en) | 1994-08-11 | 1997-08-08 | Flavor protectant closure liner compositions |
Country Status (15)
| Country | Link |
|---|---|
| US (3) | US5663223A (en) |
| EP (1) | EP0781107B1 (en) |
| JP (1) | JPH10508045A (en) |
| CN (1) | CN1145449C (en) |
| AT (1) | ATE290333T1 (en) |
| AU (1) | AU684185B2 (en) |
| BR (1) | BR9508579A (en) |
| CA (1) | CA2197296C (en) |
| DE (1) | DE69534063T2 (en) |
| DK (1) | DK0781107T3 (en) |
| ES (1) | ES2239759T3 (en) |
| MX (1) | MX9701022A (en) |
| NZ (1) | NZ287779A (en) |
| PT (1) | PT781107E (en) |
| WO (1) | WO1996004833A1 (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20070020418A1 (en) * | 2003-01-29 | 2007-01-25 | Howell Earl E Jr | Acetaldehyde scavenging by addition of active scavengers to bottle closures |
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Families Citing this family (27)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5663223A (en) * | 1994-08-11 | 1997-09-02 | Zapata Technologies, Inc. | Flavor protectant closure liner compositions |
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| BR112016020356B1 (en) | 2014-03-03 | 2020-12-08 | Hayashibara Co., Ltd | glycosyl hesperetin composition, food product, method for producing a glycosyl hesperetin composition and method for reducing the various flavors of a product comprising glycosyl hesperetin |
| DE102022206466A1 (en) | 2022-06-27 | 2023-12-28 | Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung eingetragener Verein | Use of a stabilizer composition for stabilizing halogen-free thermoplastic virgin plastics, stabilizer composition, a masterbatch or concentrate, a stabilized plastic composition, method for stabilizing halogen-free thermoplastic virgin plastics and use of the composition |
Citations (45)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2825651A (en) * | 1957-07-01 | 1958-03-04 | Carnation Co | In-package oxygen remover |
| US3135019A (en) * | 1961-06-22 | 1964-06-02 | Ernest O Aichele | Machine for applying sealing liners of thermoplastic material to bottle caps or the like |
| US3360827A (en) * | 1965-05-10 | 1968-01-02 | Ernest O. Aichele | Plastic dispensing means |
| US3547746A (en) * | 1967-07-27 | 1970-12-15 | Stanley Works | Molded embossed sealing liner having indicia |
| US3577595A (en) * | 1968-08-26 | 1971-05-04 | Zapata Industries Inc | Rotatable crown-filling machine and method for applying sealing rings of plastic to the periphery of the crown interior |
| US3691113A (en) * | 1967-08-23 | 1972-09-12 | Hercules Inc | Expanded cross-linked polymers of epihalohydrin |
| US4041209A (en) * | 1975-01-27 | 1977-08-09 | Scholle Corporation | Multiple wall packaging material containing sulfite compound |
| JPS5313724A (en) * | 1976-07-01 | 1978-02-07 | Graenges Essem Ab | Apparatus for retaining safety seattbelt of vehicle |
| US4104192A (en) * | 1976-01-26 | 1978-08-01 | Mitsubishi Gas Chemical Company Inc. | Oxygen absorbent |
| US4111323A (en) * | 1976-03-17 | 1978-09-05 | Japan Crown Cork Co., Ltd. | Crown closure |
| US4113652A (en) * | 1975-12-25 | 1978-09-12 | Mitsubishi Gas Chemical Company, Inc. | Oxygen absorbent |
| US4127503A (en) * | 1976-07-15 | 1978-11-28 | Mitsubishi Gas Chemical Company, Inc | Oxygen absorbent |
| JPS543435A (en) * | 1977-06-10 | 1979-01-11 | Hitachi Ltd | Dynamic allotment control unit for main memory |
| US4166807A (en) * | 1976-12-08 | 1979-09-04 | Mitsubishi Gas Chemical Company, Inc. | Oxygen absorbent |
| JPS5513708A (en) * | 1978-07-13 | 1980-01-30 | Mitsui Toatsu Chem Inc | Polymerization of vinyl chloride |
| US4192773A (en) * | 1977-08-24 | 1980-03-11 | Mitsubishi Gas Chemical Company, Inc. | Oxygen absorbent |
| US4199472A (en) * | 1976-07-15 | 1980-04-22 | Mitsubishi Gas Chemical Company Inc. | Oxygen absorbent composition |
| US4211681A (en) * | 1978-08-16 | 1980-07-08 | Union Carbide Corporation | Poly(ethylene oxide) compositions |
| GB2040889A (en) * | 1979-01-30 | 1980-09-03 | Metal Box Co Ltd | Closures for containers for wine or wine-based products |
| JPS562822A (en) * | 1979-06-22 | 1981-01-13 | Mitsubishi Electric Corp | Water making apparatus |
| US4278718A (en) * | 1980-01-11 | 1981-07-14 | W. R. Grace & Co. | Sealing compositions for minimizing soluble iron migration |
| US4279350A (en) * | 1979-10-11 | 1981-07-21 | Ethyl Corporation | Closure with oxygen scavenging system |
| US4287995A (en) * | 1978-11-30 | 1981-09-08 | Mitsubishi Gas Chemical Company, Inc. | Container sealing member with oxygen absorbent |
| JPS589663A (en) * | 1981-07-08 | 1983-01-20 | Higeta Shoyu Kk | Enzymatic digestion of defatted soybean and preparation of soy sauce |
| US4380597A (en) * | 1980-11-06 | 1983-04-19 | Henkel Kommanditgesellschaft Auf Aktien | Thermoplastic compositions based on vinyl chloride polymers stabilized with polyhydroxyl compounds |
| US4536409A (en) * | 1981-01-23 | 1985-08-20 | American Can Company | Oxygen scavenger |
| JPS62215101A (en) * | 1986-03-14 | 1987-09-21 | Iseki & Co Ltd | Hydraulic control device for work vehicles |
| US4702966A (en) * | 1981-01-23 | 1987-10-27 | American Can Company | Oxygen scavenger |
| US4818577A (en) * | 1987-08-20 | 1989-04-04 | Minnesota Mining And Manufacturing Company | Synthetic liner capable of resisting chemical attack and high temperature |
| EP0328337A1 (en) * | 1988-02-10 | 1989-08-16 | W.R. Grace & Co.-Conn. | Polymeric compositions and their use on container closures |
| EP0328336A1 (en) * | 1988-02-10 | 1989-08-16 | W.R. Grace & Co.-Conn. | Container closures and Materials for use in these |
| JPH01230658A (en) * | 1988-03-11 | 1989-09-14 | Asahi Chem Ind Co Ltd | Extrudable vinylidene chloride resin composition |
| US4935273A (en) * | 1989-02-01 | 1990-06-19 | Minnesota Mining And Manufacturing Company | Pressure-activated innerseals and containers using same |
| US4968514A (en) * | 1984-12-11 | 1990-11-06 | Forbes Polytech, Inc. | Beer bottle with fully reacted thermoplastic polyurethane crown capliner |
| US5100930A (en) * | 1989-07-07 | 1992-03-31 | Sumitomo Chemical Company, Limited | Food container |
| US5143763A (en) * | 1990-07-13 | 1992-09-01 | Toray Industries, Inc. | Oxygen scavenger |
| GB2257146A (en) * | 1991-07-03 | 1993-01-06 | Sandoz Ltd | Flameproofing polymeric material |
| US5202052A (en) * | 1990-09-12 | 1993-04-13 | Aquanautics Corporation | Amino polycarboxylic acid compounds as oxygen scavengers |
| US5204389A (en) * | 1988-02-10 | 1993-04-20 | W. R. Grace & Co.-Conn. | Sealed containers and sealing compositions for them |
| US5227411A (en) * | 1988-02-10 | 1993-07-13 | W. R. Grace & Co.-Conn. | Sealed containers and sealing compositions for them |
| US5265747A (en) * | 1992-07-28 | 1993-11-30 | Owens-Illinois Closure Inc. | Plastic beverage closure |
| US5308549A (en) * | 1991-11-12 | 1994-05-03 | Hoffmann-La Roche Inc. | Stabilizers for thermo plastic materials |
| US5356021A (en) * | 1993-09-30 | 1994-10-18 | H-C Industries, Inc. | Container closure with multiple liner seals |
| US5426141A (en) * | 1989-02-23 | 1995-06-20 | Fuji Photo Film Co., Ltd. | Resin composition and packaging material for photosensitive materials |
| US5663223A (en) * | 1994-08-11 | 1997-09-02 | Zapata Technologies, Inc. | Flavor protectant closure liner compositions |
Family Cites Families (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1114319B (en) * | 1959-05-02 | 1961-09-28 | Basf Ag | Molding compound made from polyolefins and a stabilizer mixture |
| DE1299537B (en) * | 1963-01-16 | 1969-07-17 | Mueller Arno | Use of a polyvinyl resin paste for the production of sealing inserts in sealing capsules |
| JPS53137244A (en) * | 1977-05-04 | 1978-11-30 | Riken Vitamin Co Ltd | Non-toxic stabilized composition of olefinic high polymer |
| JPS5434352A (en) * | 1977-08-22 | 1979-03-13 | Riken Vitamin Co Ltd | Non-toxically stabilized olefinic polymer composition |
| JPS5628229A (en) * | 1979-08-17 | 1981-03-19 | Adeka Argus Chem Co Ltd | Nontoxic and stabilized synthetic resin composition |
| JPS57194959A (en) * | 1981-05-22 | 1982-11-30 | Kishimoto Akira | Vessel cover |
| JPS5896638A (en) * | 1981-12-04 | 1983-06-08 | Asahi Chem Ind Co Ltd | Polymer composition |
| GB9123976D0 (en) * | 1991-11-12 | 1992-01-02 | Hoffmann La Roche | Stabilizers for thermoplastic materials |
| AU1305195A (en) * | 1993-12-14 | 1995-07-03 | Zapata Technologies, Inc. | Liner composition for a closure element for a fluid container |
| CA2146034A1 (en) * | 1994-05-12 | 1995-11-13 | Kenneth W. Willcox | Polymer stabilization |
-
1994
- 1994-08-11 US US08/289,170 patent/US5663223A/en not_active Expired - Fee Related
-
1995
- 1995-05-31 WO PCT/US1995/006989 patent/WO1996004833A1/en not_active Ceased
- 1995-05-31 CN CNB951954326A patent/CN1145449C/en not_active Expired - Fee Related
- 1995-05-31 JP JP8507288A patent/JPH10508045A/en active Pending
- 1995-05-31 ES ES95921578T patent/ES2239759T3/en not_active Expired - Lifetime
- 1995-05-31 PT PT95921578T patent/PT781107E/en unknown
- 1995-05-31 AU AU26611/95A patent/AU684185B2/en not_active Ceased
- 1995-05-31 DE DE69534063T patent/DE69534063T2/en not_active Expired - Lifetime
- 1995-05-31 NZ NZ287779A patent/NZ287779A/en unknown
- 1995-05-31 CA CA002197296A patent/CA2197296C/en not_active Expired - Fee Related
- 1995-05-31 EP EP95921578A patent/EP0781107B1/en not_active Expired - Lifetime
- 1995-05-31 MX MX9701022A patent/MX9701022A/en not_active IP Right Cessation
- 1995-05-31 AT AT95921578T patent/ATE290333T1/en not_active IP Right Cessation
- 1995-05-31 DK DK95921578T patent/DK0781107T3/en active
- 1995-05-31 BR BR9508579A patent/BR9508579A/en not_active IP Right Cessation
-
1997
- 1997-08-08 US US08/908,577 patent/US5863964A/en not_active Ceased
-
1999
- 1999-09-16 US US09/398,935 patent/USRE36815E/en not_active Expired - Fee Related
Patent Citations (47)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2825651A (en) * | 1957-07-01 | 1958-03-04 | Carnation Co | In-package oxygen remover |
| US3135019A (en) * | 1961-06-22 | 1964-06-02 | Ernest O Aichele | Machine for applying sealing liners of thermoplastic material to bottle caps or the like |
| US3360827A (en) * | 1965-05-10 | 1968-01-02 | Ernest O. Aichele | Plastic dispensing means |
| US3547746A (en) * | 1967-07-27 | 1970-12-15 | Stanley Works | Molded embossed sealing liner having indicia |
| US3691113A (en) * | 1967-08-23 | 1972-09-12 | Hercules Inc | Expanded cross-linked polymers of epihalohydrin |
| US3577595A (en) * | 1968-08-26 | 1971-05-04 | Zapata Industries Inc | Rotatable crown-filling machine and method for applying sealing rings of plastic to the periphery of the crown interior |
| US4041209A (en) * | 1975-01-27 | 1977-08-09 | Scholle Corporation | Multiple wall packaging material containing sulfite compound |
| US4113652A (en) * | 1975-12-25 | 1978-09-12 | Mitsubishi Gas Chemical Company, Inc. | Oxygen absorbent |
| US4104192A (en) * | 1976-01-26 | 1978-08-01 | Mitsubishi Gas Chemical Company Inc. | Oxygen absorbent |
| US4111323A (en) * | 1976-03-17 | 1978-09-05 | Japan Crown Cork Co., Ltd. | Crown closure |
| JPS5313724A (en) * | 1976-07-01 | 1978-02-07 | Graenges Essem Ab | Apparatus for retaining safety seattbelt of vehicle |
| US4127503A (en) * | 1976-07-15 | 1978-11-28 | Mitsubishi Gas Chemical Company, Inc | Oxygen absorbent |
| US4199472A (en) * | 1976-07-15 | 1980-04-22 | Mitsubishi Gas Chemical Company Inc. | Oxygen absorbent composition |
| US4166807A (en) * | 1976-12-08 | 1979-09-04 | Mitsubishi Gas Chemical Company, Inc. | Oxygen absorbent |
| JPS543435A (en) * | 1977-06-10 | 1979-01-11 | Hitachi Ltd | Dynamic allotment control unit for main memory |
| US4192773A (en) * | 1977-08-24 | 1980-03-11 | Mitsubishi Gas Chemical Company, Inc. | Oxygen absorbent |
| JPS5513708A (en) * | 1978-07-13 | 1980-01-30 | Mitsui Toatsu Chem Inc | Polymerization of vinyl chloride |
| US4211681A (en) * | 1978-08-16 | 1980-07-08 | Union Carbide Corporation | Poly(ethylene oxide) compositions |
| US4287995A (en) * | 1978-11-30 | 1981-09-08 | Mitsubishi Gas Chemical Company, Inc. | Container sealing member with oxygen absorbent |
| GB2040889A (en) * | 1979-01-30 | 1980-09-03 | Metal Box Co Ltd | Closures for containers for wine or wine-based products |
| JPS562822A (en) * | 1979-06-22 | 1981-01-13 | Mitsubishi Electric Corp | Water making apparatus |
| US4279350A (en) * | 1979-10-11 | 1981-07-21 | Ethyl Corporation | Closure with oxygen scavenging system |
| US4278718A (en) * | 1980-01-11 | 1981-07-14 | W. R. Grace & Co. | Sealing compositions for minimizing soluble iron migration |
| US4380597A (en) * | 1980-11-06 | 1983-04-19 | Henkel Kommanditgesellschaft Auf Aktien | Thermoplastic compositions based on vinyl chloride polymers stabilized with polyhydroxyl compounds |
| US4536409A (en) * | 1981-01-23 | 1985-08-20 | American Can Company | Oxygen scavenger |
| US4702966A (en) * | 1981-01-23 | 1987-10-27 | American Can Company | Oxygen scavenger |
| JPS589663A (en) * | 1981-07-08 | 1983-01-20 | Higeta Shoyu Kk | Enzymatic digestion of defatted soybean and preparation of soy sauce |
| US4968514A (en) * | 1984-12-11 | 1990-11-06 | Forbes Polytech, Inc. | Beer bottle with fully reacted thermoplastic polyurethane crown capliner |
| JPS62215101A (en) * | 1986-03-14 | 1987-09-21 | Iseki & Co Ltd | Hydraulic control device for work vehicles |
| US4818577A (en) * | 1987-08-20 | 1989-04-04 | Minnesota Mining And Manufacturing Company | Synthetic liner capable of resisting chemical attack and high temperature |
| US5227411A (en) * | 1988-02-10 | 1993-07-13 | W. R. Grace & Co.-Conn. | Sealed containers and sealing compositions for them |
| EP0328337A1 (en) * | 1988-02-10 | 1989-08-16 | W.R. Grace & Co.-Conn. | Polymeric compositions and their use on container closures |
| EP0328336A1 (en) * | 1988-02-10 | 1989-08-16 | W.R. Grace & Co.-Conn. | Container closures and Materials for use in these |
| US5075362A (en) * | 1988-02-10 | 1991-12-24 | W. R. Grace & Co.-Conn. | Sealed containers and sealing compositions for them |
| US5106886A (en) * | 1988-02-10 | 1992-04-21 | W. R. Grace & Co.-Conn. | Sealed containers and sealing compositions for them |
| US5204389A (en) * | 1988-02-10 | 1993-04-20 | W. R. Grace & Co.-Conn. | Sealed containers and sealing compositions for them |
| JPH01230658A (en) * | 1988-03-11 | 1989-09-14 | Asahi Chem Ind Co Ltd | Extrudable vinylidene chloride resin composition |
| US4935273A (en) * | 1989-02-01 | 1990-06-19 | Minnesota Mining And Manufacturing Company | Pressure-activated innerseals and containers using same |
| US5426141A (en) * | 1989-02-23 | 1995-06-20 | Fuji Photo Film Co., Ltd. | Resin composition and packaging material for photosensitive materials |
| US5100930A (en) * | 1989-07-07 | 1992-03-31 | Sumitomo Chemical Company, Limited | Food container |
| US5143763A (en) * | 1990-07-13 | 1992-09-01 | Toray Industries, Inc. | Oxygen scavenger |
| US5202052A (en) * | 1990-09-12 | 1993-04-13 | Aquanautics Corporation | Amino polycarboxylic acid compounds as oxygen scavengers |
| GB2257146A (en) * | 1991-07-03 | 1993-01-06 | Sandoz Ltd | Flameproofing polymeric material |
| US5308549A (en) * | 1991-11-12 | 1994-05-03 | Hoffmann-La Roche Inc. | Stabilizers for thermo plastic materials |
| US5265747A (en) * | 1992-07-28 | 1993-11-30 | Owens-Illinois Closure Inc. | Plastic beverage closure |
| US5356021A (en) * | 1993-09-30 | 1994-10-18 | H-C Industries, Inc. | Container closure with multiple liner seals |
| US5663223A (en) * | 1994-08-11 | 1997-09-02 | Zapata Technologies, Inc. | Flavor protectant closure liner compositions |
Non-Patent Citations (12)
| Title |
|---|
| Environ. Science Technology, vol. 21, No. 3, 1987, "Drinking-water Treatment With Ozone", William H. Glaze, pp. 224-230. |
| Environ. Science Technology, vol. 21, No. 3, 1987, Drinking water Treatment With Ozone , William H. Glaze, pp. 224 230. * |
| Journal AWWA, Research and Technology, "Effects of Ozonation on Tastes and Odor", Oct. 1988, Christophe Anselme, et al., pp. 45-51. |
| Journal AWWA, Research and Technology, "Ozonation: Assessing Its Role in the Formation and Control of Disinfection By-products", Joseph G. Jacangelo, et al., Aug. 1989, pp. 74-84. |
| Journal AWWA, Research and Technology, Effects of Ozonation on Tastes and Odor , Oct. 1988, Christophe Anselme, et al., pp. 45 51. * |
| Journal AWWA, Research and Technology, Evaluation of Ozonation By products From Two California Surface Waters, William H. Glaze et al., Aug. 1989, pp. 66 73. * |
| Journal AWWA, Research and Technology, Evaluation of Ozonation By-products From Two California Surface Waters, William H. Glaze et al., Aug. 1989, pp. 66-73. |
| Journal AWWA, Research and Technology, Ozonation: Assessing Its Role in the Formation and Control of Disinfection By products , Joseph G. Jacangelo, et al., Aug. 1989, pp. 74 84. * |
| Roche Brochure, Why is Ronotec 201 the Smarter AO , Oct. 1992. * |
| Roche Bulletin Product Data, Ronotec 201 , Sep. 29, 1989. * |
| Roche® Brochure, "Why is Ronotec® 201 the Smarter AO?", Oct. 1992. |
| Roche® Bulletin--Product Data, "Ronotec® 201", Sep. 29, 1989. |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20070020418A1 (en) * | 2003-01-29 | 2007-01-25 | Howell Earl E Jr | Acetaldehyde scavenging by addition of active scavengers to bottle closures |
| US20110143005A1 (en) * | 2005-09-02 | 2011-06-16 | Anilkumar Ganapati Gaonkar | Methods for the Application of Ingredients to the Inside of a Straw |
| US8409643B2 (en) | 2005-09-02 | 2013-04-02 | Kraft Foods Group Brands Llc | Methods for the application of ingredients to the inside of a straw |
Also Published As
| Publication number | Publication date |
|---|---|
| EP0781107B1 (en) | 2005-03-09 |
| EP0781107A1 (en) | 1997-07-02 |
| EP0781107A4 (en) | 2001-03-07 |
| US5663223A (en) | 1997-09-02 |
| AU684185B2 (en) | 1997-12-04 |
| ATE290333T1 (en) | 2005-03-15 |
| AU2661195A (en) | 1996-03-07 |
| US5863964A (en) | 1999-01-26 |
| PT781107E (en) | 2005-07-29 |
| DE69534063T2 (en) | 2006-04-13 |
| CA2197296C (en) | 2004-08-17 |
| NZ287779A (en) | 1998-04-27 |
| MX9701022A (en) | 1997-05-31 |
| DE69534063D1 (en) | 2005-04-14 |
| WO1996004833A1 (en) | 1996-02-22 |
| BR9508579A (en) | 1997-11-11 |
| DK0781107T3 (en) | 2005-07-11 |
| ES2239759T3 (en) | 2005-10-01 |
| CA2197296A1 (en) | 1996-02-22 |
| JPH10508045A (en) | 1998-08-04 |
| CN1166127A (en) | 1997-11-26 |
| CN1145449C (en) | 2004-04-14 |
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