AU758893B2 - New uses for oxygen scavenging compositions - Google Patents
New uses for oxygen scavenging compositions Download PDFInfo
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- AU758893B2 AU758893B2 AU87230/98A AU8723098A AU758893B2 AU 758893 B2 AU758893 B2 AU 758893B2 AU 87230/98 A AU87230/98 A AU 87230/98A AU 8723098 A AU8723098 A AU 8723098A AU 758893 B2 AU758893 B2 AU 758893B2
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- AU
- Australia
- Prior art keywords
- oxygen scavenging
- organic compound
- oxygen
- coating
- composition
- 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
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- 239000001301 oxygen Substances 0.000 title description 109
- 229910052760 oxygen Inorganic materials 0.000 title description 109
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 title description 107
- 230000002000 scavenging effect Effects 0.000 title description 86
- 239000000203 mixture Substances 0.000 title description 81
- 239000010410 layer Substances 0.000 description 81
- 150000002894 organic compounds Chemical class 0.000 description 39
- 238000000576 coating method Methods 0.000 description 23
- 239000011248 coating agent Substances 0.000 description 21
- 229920000642 polymer Polymers 0.000 description 18
- 229920001577 copolymer Polymers 0.000 description 14
- 239000007788 liquid Substances 0.000 description 12
- 150000002926 oxygen Chemical class 0.000 description 11
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 10
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 10
- 230000004888 barrier function Effects 0.000 description 10
- 239000003054 catalyst Substances 0.000 description 10
- 239000007789 gas Substances 0.000 description 10
- 239000000463 material Substances 0.000 description 10
- -1 polyethylene naphthalate Polymers 0.000 description 10
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 9
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 9
- 229910001882 dioxygen Inorganic materials 0.000 description 9
- 238000005286 illumination Methods 0.000 description 9
- 230000003647 oxidation Effects 0.000 description 9
- 238000007254 oxidation reaction Methods 0.000 description 9
- 229910052723 transition metal Inorganic materials 0.000 description 9
- 150000003624 transition metals Chemical class 0.000 description 9
- 230000005283 ground state Effects 0.000 description 8
- 239000005022 packaging material Substances 0.000 description 8
- 230000009467 reduction Effects 0.000 description 8
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 6
- 239000005977 Ethylene Substances 0.000 description 6
- 238000006243 chemical reaction Methods 0.000 description 6
- 238000010992 reflux Methods 0.000 description 6
- 229920005989 resin Polymers 0.000 description 6
- 239000011347 resin Substances 0.000 description 6
- 239000004698 Polyethylene Substances 0.000 description 5
- 235000013305 food Nutrition 0.000 description 5
- 229910052757 nitrogen Inorganic materials 0.000 description 5
- 229920003023 plastic Polymers 0.000 description 5
- 239000004033 plastic Substances 0.000 description 5
- 239000000047 product Substances 0.000 description 5
- 239000011541 reaction mixture Substances 0.000 description 5
- PNEYBMLMFCGWSK-UHFFFAOYSA-N Alumina Chemical compound [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- 239000000853 adhesive Substances 0.000 description 4
- 239000004411 aluminium Substances 0.000 description 4
- 229910052782 aluminium Inorganic materials 0.000 description 4
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 4
- PYKYMHQGRFAEBM-UHFFFAOYSA-N anthraquinone Natural products CCC(=O)c1c(O)c2C(=O)C3C(C=CC=C3O)C(=O)c2cc1CC(=O)OC PYKYMHQGRFAEBM-UHFFFAOYSA-N 0.000 description 4
- 239000012298 atmosphere Substances 0.000 description 4
- 239000011324 bead Substances 0.000 description 4
- 239000011261 inert gas Substances 0.000 description 4
- 239000005020 polyethylene terephthalate Substances 0.000 description 4
- 229920000139 polyethylene terephthalate Polymers 0.000 description 4
- 239000000565 sealant Substances 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- AZQWKYJCGOJGHM-UHFFFAOYSA-N 1,4-benzoquinone Chemical compound O=C1C=CC(=O)C=C1 AZQWKYJCGOJGHM-UHFFFAOYSA-N 0.000 description 3
- UFQHFMGRRVQFNA-UHFFFAOYSA-N 3-(dimethylamino)propyl prop-2-enoate Chemical compound CN(C)CCCOC(=O)C=C UFQHFMGRRVQFNA-UHFFFAOYSA-N 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 3
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 229920001328 Polyvinylidene chloride Polymers 0.000 description 3
- 230000001070 adhesive effect Effects 0.000 description 3
- 239000005030 aluminium foil Substances 0.000 description 3
- 238000004458 analytical method Methods 0.000 description 3
- 150000004056 anthraquinones Chemical class 0.000 description 3
- 235000012846 chilled/fresh pasta Nutrition 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 239000005038 ethylene vinyl acetate Substances 0.000 description 3
- 238000001125 extrusion Methods 0.000 description 3
- 238000011049 filling Methods 0.000 description 3
- 238000001914 filtration Methods 0.000 description 3
- 239000005021 flexible packaging material Substances 0.000 description 3
- 238000011010 flushing procedure Methods 0.000 description 3
- 239000011521 glass Substances 0.000 description 3
- 239000001257 hydrogen Substances 0.000 description 3
- 229910052739 hydrogen Inorganic materials 0.000 description 3
- 239000004922 lacquer Substances 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 239000000178 monomer Substances 0.000 description 3
- 238000004806 packaging method and process Methods 0.000 description 3
- 229920003207 poly(ethylene-2,6-naphthalate) Polymers 0.000 description 3
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 3
- 239000011112 polyethylene naphthalate Substances 0.000 description 3
- 239000005033 polyvinylidene chloride Substances 0.000 description 3
- 239000002356 single layer Substances 0.000 description 3
- 125000001424 substituent group Chemical group 0.000 description 3
- 230000001960 triggered effect Effects 0.000 description 3
- YUQBROWLLZRNHO-UHFFFAOYSA-N 1-(9,10-dioxoanthracen-1-yl)ethyl prop-2-enoate Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C=CC=C2C(OC(=O)C=C)C YUQBROWLLZRNHO-UHFFFAOYSA-N 0.000 description 2
- 229920001824 Barex® Polymers 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 2
- 229920000219 Ethylene vinyl alcohol Polymers 0.000 description 2
- 229920001944 Plastisol Polymers 0.000 description 2
- 239000004743 Polypropylene Substances 0.000 description 2
- 229910000831 Steel Inorganic materials 0.000 description 2
- 238000003848 UV Light-Curing Methods 0.000 description 2
- QRSFFHRCBYCWBS-UHFFFAOYSA-N [O].[O] Chemical compound [O].[O] QRSFFHRCBYCWBS-UHFFFAOYSA-N 0.000 description 2
- 239000012790 adhesive layer Substances 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 210000003298 dental enamel Anatomy 0.000 description 2
- 230000004927 fusion Effects 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 229910044991 metal oxide Inorganic materials 0.000 description 2
- 150000004706 metal oxides Chemical group 0.000 description 2
- 239000003094 microcapsule Substances 0.000 description 2
- PZRHRDRVRGEVNW-UHFFFAOYSA-N milrinone Chemical compound N1C(=O)C(C#N)=CC(C=2C=CN=CC=2)=C1C PZRHRDRVRGEVNW-UHFFFAOYSA-N 0.000 description 2
- 229960003574 milrinone Drugs 0.000 description 2
- 239000011087 paperboard Substances 0.000 description 2
- 239000004999 plastisol Substances 0.000 description 2
- 229920000098 polyolefin Polymers 0.000 description 2
- 229920001155 polypropylene Polymers 0.000 description 2
- 238000003825 pressing Methods 0.000 description 2
- 239000002516 radical scavenger Substances 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 238000007789 sealing Methods 0.000 description 2
- 239000010959 steel Substances 0.000 description 2
- 238000003860 storage Methods 0.000 description 2
- 238000003786 synthesis reaction Methods 0.000 description 2
- VXUYXOFXAQZZMF-UHFFFAOYSA-N titanium(IV) isopropoxide Chemical compound CC(C)O[Ti](OC(C)C)(OC(C)C)OC(C)C VXUYXOFXAQZZMF-UHFFFAOYSA-N 0.000 description 2
- HVLLSGMXQDNUAL-UHFFFAOYSA-N triphenyl phosphite Chemical compound C=1C=CC=CC=1OP(OC=1C=CC=CC=1)OC1=CC=CC=C1 HVLLSGMXQDNUAL-UHFFFAOYSA-N 0.000 description 2
- RIOQSEWOXXDEQQ-UHFFFAOYSA-N triphenylphosphine Chemical compound C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 RIOQSEWOXXDEQQ-UHFFFAOYSA-N 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- BHMLFPOTZYRDKA-IRXDYDNUSA-N (2s)-2-[(s)-(2-iodophenoxy)-phenylmethyl]morpholine Chemical compound IC1=CC=CC=C1O[C@@H](C=1C=CC=CC=1)[C@H]1OCCNC1 BHMLFPOTZYRDKA-IRXDYDNUSA-N 0.000 description 1
- FRASJONUBLZVQX-UHFFFAOYSA-N 1,4-naphthoquinone Chemical compound C1=CC=C2C(=O)C=CC(=O)C2=C1 FRASJONUBLZVQX-UHFFFAOYSA-N 0.000 description 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- SJEBAWHUJDUKQK-UHFFFAOYSA-N 2-ethylanthraquinone Chemical compound C1=CC=C2C(=O)C3=CC(CC)=CC=C3C(=O)C2=C1 SJEBAWHUJDUKQK-UHFFFAOYSA-N 0.000 description 1
- AGIJRRREJXSQJR-UHFFFAOYSA-N 2h-thiazine Chemical compound N1SC=CC=C1 AGIJRRREJXSQJR-UHFFFAOYSA-N 0.000 description 1
- RZVHIXYEVGDQDX-UHFFFAOYSA-N 9,10-anthraquinone Chemical compound C1=CC=C2C(=O)C3=CC=CC=C3C(=O)C2=C1 RZVHIXYEVGDQDX-UHFFFAOYSA-N 0.000 description 1
- 229940076442 9,10-anthraquinone Drugs 0.000 description 1
- 238000003855 Adhesive Lamination Methods 0.000 description 1
- 239000004342 Benzoyl peroxide Substances 0.000 description 1
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 1
- 229920000089 Cyclic olefin copolymer Polymers 0.000 description 1
- IMROMDMJAWUWLK-UHFFFAOYSA-N Ethenol Chemical compound OC=C IMROMDMJAWUWLK-UHFFFAOYSA-N 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical group COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 1
- 229940123973 Oxygen scavenger Drugs 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- 241000206607 Porphyra umbilicalis Species 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- XQAXGZLFSSPBMK-UHFFFAOYSA-M [7-(dimethylamino)phenothiazin-3-ylidene]-dimethylazanium;chloride;trihydrate Chemical compound O.O.O.[Cl-].C1=CC(=[N+](C)C)C=C2SC3=CC(N(C)C)=CC=C3N=C21 XQAXGZLFSSPBMK-UHFFFAOYSA-M 0.000 description 1
- 238000002835 absorbance Methods 0.000 description 1
- 239000002998 adhesive polymer Substances 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 239000004760 aramid Substances 0.000 description 1
- 229920003235 aromatic polyamide Polymers 0.000 description 1
- 125000000751 azo group Chemical group [*]N=N[*] 0.000 description 1
- 235000013405 beer Nutrition 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 235000019400 benzoyl peroxide Nutrition 0.000 description 1
- 238000000071 blow moulding Methods 0.000 description 1
- 229910002091 carbon monoxide Inorganic materials 0.000 description 1
- 150000001728 carbonyl compounds Chemical class 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 238000010382 chemical cross-linking Methods 0.000 description 1
- 238000001311 chemical methods and process Methods 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 230000003635 deoxygenating effect Effects 0.000 description 1
- 229910003460 diamond Inorganic materials 0.000 description 1
- 239000010432 diamond Substances 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 230000005670 electromagnetic radiation Effects 0.000 description 1
- 238000010894 electron beam technology Methods 0.000 description 1
- 229920006334 epoxy coating Polymers 0.000 description 1
- 125000003700 epoxy group Chemical group 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- UFRKOOWSQGXVKV-UHFFFAOYSA-N ethene;ethenol Chemical compound C=C.OC=C UFRKOOWSQGXVKV-UHFFFAOYSA-N 0.000 description 1
- 235000019439 ethyl acetate Nutrition 0.000 description 1
- 239000004715 ethylene vinyl alcohol Substances 0.000 description 1
- 238000007765 extrusion coating Methods 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 238000004817 gas chromatography Methods 0.000 description 1
- 230000036571 hydration Effects 0.000 description 1
- 238000006703 hydration reaction Methods 0.000 description 1
- 239000005001 laminate film Substances 0.000 description 1
- 235000021056 liquid food Nutrition 0.000 description 1
- 235000013372 meat Nutrition 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 229960000907 methylthioninium chloride Drugs 0.000 description 1
- 230000000813 microbial effect Effects 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 150000004767 nitrides Chemical class 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- 239000000123 paper Substances 0.000 description 1
- 239000012466 permeate Substances 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 239000000825 pharmaceutical preparation Substances 0.000 description 1
- 150000003003 phosphines Chemical class 0.000 description 1
- AQSJGOWTSHOLKH-UHFFFAOYSA-N phosphite(3-) Chemical class [O-]P([O-])[O-] AQSJGOWTSHOLKH-UHFFFAOYSA-N 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 230000001376 precipitating effect Effects 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000000750 progressive effect Effects 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 150000004053 quinones Chemical class 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 235000021057 semi-liquid food Nutrition 0.000 description 1
- LIVNPJMFVYWSIS-UHFFFAOYSA-N silicon monoxide Chemical class [Si-]#[O+] LIVNPJMFVYWSIS-UHFFFAOYSA-N 0.000 description 1
- 229910052814 silicon oxide Inorganic materials 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000000935 solvent evaporation Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 150000003460 sulfonic acids Chemical class 0.000 description 1
- 150000003464 sulfur compounds Chemical class 0.000 description 1
- 229920001897 terpolymer Polymers 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
- 150000007970 thio esters Chemical class 0.000 description 1
- 150000003568 thioethers Chemical class 0.000 description 1
- 150000003573 thiols Chemical class 0.000 description 1
- 238000002211 ultraviolet spectrum Methods 0.000 description 1
- 238000009461 vacuum packaging Methods 0.000 description 1
Landscapes
- Packages (AREA)
- Wrappers (AREA)
Description
WO 99/10251 PCT/AU98/00671 1 NEW USES FOR OXYGEN SCAVENGING
COMPOSITIONS
Field of the Invention: This invention relates to novel uses of the oxygen scavenging compositions described in the co-pending Australian patent application No.
55537/94. In particular. the invention relates to novel uses of oxygen scavenging compositions in packaging materials comprising a gas and vapour barrier-forming layer or coating.
Background of the Invention: A wide variety of foods and other materials are susceptible to loss in quality during storage under atmospheric levels of oxygen. The damage can arise from chemical oxidation of the product, from microbial growth, and from attack by vermin much of which may be avoided by reducing the oxygen availability in the environment of the materials. In the field of packaging, relatively low-oxygen atmospheres have traditionally been generated by vacuum packing and inert gas flushing. Such methods are not, however, generally applicable for various reasons. For example: soft porous foods such as cakes cannot be subjected to strong vacuum; fast filling speeds generally preclude substantial evacuation of, or thorough inert gas flushing of, food packages: filling some gas-flushed containers, such as beer bottles often results in occlusion of air: evacuation or flushing offers no residual capacity for removal of oxygen, which may have desorbed from the food or entered the package by leakage or permeation.
As a consequence there has been much interest in chemical techniques for generating low-oxygen atmospheres and deoxygenating liquid or semiliquid foods.
In the abovementioned Australian patent application No. 55537/94 (the entire disclosure of which is incorporated herein by reference), the present applicants describe novel oxygen scavenging compositions which may be readily activated or "triggered" (ie. brought to their oxygen scavenging form) as required by exposure to predetermined conditions, for example, light of a certain intensity or wavelng&()i-fr (Xeir lication of heat, y- SUBSTITUTE SHEET (Rule 26) WO 99/10251 PCT/AU98/00671 2 irradiation, corona discharge or an electron beam. These compositions (and packaging materials including the compositions) may therefore be stored under standard conditions, then triggered to the activated state just prior to use. The oxygen scavenging compositions, once activated, are capable of continuing to scavenge oxygen from an oxygenated atmosphere or liquid in substantial darkness for periods ranging from up to a few minutes or hours to over 100 days.
The novel oxygen scavenging compositions described in application No. 55537/94 are hereinafter referred to as "the oxygen scavenging compositions". These compositions comprise at least one reducible organic compound which is reduced and/or subsequently oxidised independently of each of constant illumination with visible light and the presence of a transition metal catalyst. The most preferred reducible organic compounds are quinones such as benzoquinone. anthraquinone (eg. 9,10-anthraquinone) and napthoquinone (eg. 1,4-napthoquinone): photoreducible dyes (e.g.
methylene blue, azo, thiazine, indigoid and triarylmethane compounds); and carbonyl compounds which have absorbance in the UV spectrum particularly, when provided in a in polymerised, copolymerised, or oligomerised form.
In addition, the oxygen scavenging compositions described in application No. 55537/94 may include a scavenging component reactive to activated oxygen species peroxide) which may be generated during the scavenging of molecular oxygen. Preferred examples of the activated oxygen scavenging component include antioxidants. amines. organic phosphines triphenylphosphine) and organic phosphites triphenylphosphite) and sulfur compounds such as thiols, thioethers and thioesters.
Alternatively, the activated oxygen scavenging component may be embodied within the reducible organic compound itself, for example a quinone having an amine group.
Further, the compositions may include a source of labile hydrogen or electrons which may be abstracted by the reducible organic compound as it is brought to its activated state. Such sources of labile hydrogen or electrons include compounds such as the salts of sulfonic or carboxylic acids.
As described in application No. 55537/94, the at least one reducible organic compound, the activated oxygen scavenging component and/or the source of labile hydrogen or electrons may be in the form of a polymer, WO 99/10251 PCT/AU98/00671 3 copolymer or oligomer. thereby providing an advantage of permitting the use of the oxygen scavenging compositions in the form of films (monolayer and multilayer) for a wide variety of applications. In multilayer laminate films, the at least one reducible organic compound and activated oxygen scavenging component may be provided in the same layer or in distinct layers.
The copolymerised form of the reducible organic compound is a copolymer of a monomer containing the reducible organic compound bound with one or more monomers which might be used in packaging polymers.
It is evident from the descriptions of uses in application No. 55537/94, that the oxygen scavenging compositions can be utilised in a wide variety of packaging materials and package forms. However, the applicants have now recognised further novel uses and modes of use for the oxygen scavenging compositions.
Disclosure of the Invention: Thus, in a first aspect, the present invention provides a flexible packaging material comprising a film. co-extrusion or laminate comprising one or more layers of an oxygen scavenging composition(s) in combination with at least one gas and vapour barrier-forming layer or coating, wherein said oxygen scavenging composition(s) comprises at least one reducible organic compound which is reduced when the composition(s) is subjected to predetermined conditions, the reduced form of the organic compound(s) being oxidisable by ground state molecular oxygen, and wherein the reduction and/or subsequent oxidation of the organic compound(s) occurs independently of each of constant illumination with visible light and the presence of a transition metal catalyst.
Preferably, the said barrier-forming layer or coating is an oxygen barrier-forming layer or coating such as a film layer of a high oxygen barrier polymer polyvinyl alcohol. ethylene vinyl alcohol copolymer and polyethylene naphthalate) which may also be coated with a further barrier polymer such as polyvinylidene chloride or its copolymers, or a coating of a substance selected from the group consisting of carbon (particularly in the crystalline form of diamond), aluminium, aluminium oxide, and oxides and nitrides of metals, including silicon oxides.
WO 99/10251 PCT/AU98/00671 4 The one or more layers of the oxygen scavenging composition may be laminated or extrusion-coated onto a barrier-forming layer. Barrier-forming coatings may be applied directly to the surface of a layer of the oxygen scavenging composition or, for example, to a laminated film. Barrier-forming coatings may be applied by vacuum techniques which are well known to persons skilled in the art.
The innermost layer(s) comprising the oxygen scavenging composition ("the scavenger layer(s)") or another fusible layer or an adhesive layer, may be considered as forming "the sealant layer" of the packaging material. The flexible packaging material according to the first aspect may further comprise one or more layers of a solid packaging material such as aluminium foil or paper. Further, the oxygen scavenging composition may be blended or dispersed in one or more layers of the flexible packaging material. Where the oxygen scavenging composition includes an activated oxygen scavenging component, the at least one reducible organic compound and the activated oxygen scavenging component may be present in the same or distinct layers.
In use, the gas and vapour barrier-forming layer or coating will normally be present on the outside of the package relative to the scavenging layer facing the surrounding environment. The oxygen scavenging layer(s) are, therefore, normally adjacent to the package contents, although contact between the contents and the oxygen scavenging layer(s) may be avoided by providing a space within the package and/or by providing an inner, relatively high gas-permeable, heat seal "sealant") layer or layers. Where an oxygen scavenging layer contacts the package contents, the oxygen scavenging layer would normally also be a sealant layer.
It may also be advantageous to provide the packaging material with an additional layer or layers to provide strength or other properties. Where thermoplastic, these additional layer(s) can be coextruded, extrusion laminated or adhesive laminated (see Example The oxygen scavenging layer may be the tie layer in coextrusions or the adhesive layer (in which case it would include an adhesive agent or polymer) in adhesive laminations.
Preferably, the oxygen scavenging layer(s) may comprise a blend or mixture of the oxygen scavenging composition and a polymer(s) such as a polyolefin polyethylene, polypropylene and copolymers thereof) or copolymer of an olefin including modifying monomers such as acrylic acid or WO 99/10251 PCT/AU98/00671 methacrylic acid and their esters and salts, or ethylene vinyl acetate copolymer and its terpolymers.
The concentration of the at least one reducible organic compound or, where polymerised, copolymerised or oligomerised, the reducible substituent an anthraquinonyl group). may be varied to provide any required oxygen scavenging rate or capability to react with the quantity of oxygen expected to enter the package by leakage or permeation during its useful life. The concentration of the reducible organic compound or group will therefore vary between 0.01% and 99.9% of the oxygen scavenging layer, preferably between 0.01% and 50% The laminates or coextrusions described above may be used in the production of liquid cartonboard for use in. for example, the manufacture of brick-shape and gable-topped cartons for liquids.
Thus, in a second aspect. the present invention provides a carton for liquids manufactured from liquid cartonboard comprising one or more layers of an oxygen scavenging composition(s) in combination with at least one gas and vapour barrier-forming layer or coating, wherein said oxygen scavenging composition(s) comprises at least one reducible organic compound which is reduced when the composition is subjected to predetermined conditions, the reduced form of the organic compound(s) being oxidisable by ground state molecular oxygen, and wherein the reduction and/or subsequent oxidation of the organic compound(s) occurs independently of each of constant illumination with visible light and the presence of a transition metal catalyst.
Such cartons may vary in capacity from 100 ml to 50 litres, preferably from 250 ml to 10 litres. The barrier-forming layer or coating is preferably an oxygen barrier-forming layer or coating and may be as described above in connection to the first aspect of the invention, but is preferably a layer of aluminium foil or a polymer that is metal-oxide coated, or is coated with polyvinylidene chloride or a vacuum-deposited coating of aluminium.
The cartons according to the second aspect of the invention may be particularly valuable in applications where the carton is to contain a headspace containing oxygen or where the liquid contents contain substantial dissolved oxygen.
Film forms of the packaging material of the first aspect may also be used to package liquids, for example, in a bag-in-box type package.
WO 99/10251 PCT/AU98/00671 6 Thus, in a third aspect. the present invention provides a bag-in-box package for containing liquids including a bag comprising one or more film layers of an oxygen scavenging composition(s) in combination with at least one gas and vapour barrier-forming layer or coating, wherein said oxygen scavenging composition(s) comprises at least one reducible organic compound which is reduced when the composition is subjected to predetermined conditions. the reduced form of the organic compound(s) being oxidisable by ground state molecular oxygen. and wherein the reduction and/or subsequent oxidation of the organic compound(s) occurs independently of each of constant illumination with visible light and the presence of a transition metal catalyst.
The "box" in which thebag is contained may be any of the usual containers in which such bags are held commercially. These containers include fibreboard boxes. fibreboard cartons fibreboard containers on pallets, timber or metal structures or drums. Paper or paperboard may also be used to make such containers as may plastics.
The bag included in the bag-in-box package may comprise one layer or two separate ("structural") film layers separated by a gas space and formed into a pouch or bag by sealing at the edges. Both single and duplex construction, which are well known to the art. provides a package which collapses readily as the liquid contents are withdrawn. In some embodiments, a fitting for a tap will be affixed to the bag so as to allow filling of the package, often under aseptic conditions, followed by later (progressive) dispensing after attachment of the tap itself. The tap and/or its fitting may be constructed of a plastic or other polymer composition containing the oxygen scavenging composition. This is particularly valuable since much of the oxygen ingress that occurs in present packages of this type takes place through the tap and its fittings.
Preferably, the barrier-forming layer or coating is an oxygen barrierforming layer or coating.
The one or more film layers of the oxygen scavenging composition may be located closest to the liquid contents and/or may form one or more outer layers which are inside the bag relative to the barrier-forming layer. An additional film layer or layers of the oxygen scavenging composition may also be included between the structural layers of the bag. Where the oxygen scavenging composition includes an activated oxygen scavenging WO 99/10251 PCT/AU98/00671 7 component, the reducible organic compound and the activated oxygen scavenging component may be present in distinct layers.
The capacity of bag-in-box packages according to the invention may be from 300ml to 1.5 tonnes, preferably 375ml to 1.5 tonnes. The volume of oxygen initially within the bag can range from 5ml to 1 litre. The concentration of the reducible organic compound or. where polymerised, the reducible substituent. in the oxygen scavenging layer(s) and/or tap assembly may be varied to allow for removal of oxygen as it permeates the packaging material and/or as it leaks through the tap assembly and/or package seals.
In a fourth aspect. the present invention provides a thernoformed tray, cup or tub comprising an oxygen scavenging composition(s) in combination with at least one gas and vapour barrier-forining layer or coating, wherein said oxygen scavenging composition(s) comprises at least one reducible organic compound which is reduced when the composition is subjected to predetermined conditions, the reduced form of the organic compound(s) being oxidisable by ground state molecular oxygen. and wherein the reduction and/or subsequent oxidation of the organic compound(s) occurs independently of each of constant illumination with visible light and the presence of a transition metal catalyst.
The oxygen scavenging coimposition may be a polymer or copolymer, or otherwise dispersed in a polymer or copolymer. used to manufacture the tray, cup or tub. Alternatively or additionally, the oxygen scavenging composition may be present in a layer or layers of a multilayer thermoformed film or sheet used to thermoform the tray. cup or tub (see Example 2).
Preferably, the oxygen scavenging layer(s) will be located closer to the insides of the tray, cup or tub than the barrier-forming layer. Again, the barrier-forming layer or coating is preferably an oxygen barrier-forming layer or coating. Also, where the oxygen scavenging composition includes an activated oxygen scavenging component, the reducible organic compound and the activated oxygen scavenging component may be present in distinct layers.
Additionally, the oxygen scavenging composition may be included in the layer of lidding film between the barrier-forming layer and the package contents. In this embodiment, the lidding film layer would usually be sealable to the opening of the container. Alternatively, the oxygen scavenging composition may form, be blended or otherwise incorporated into WO 99/10251 PCT/AU98/00671 8 a layer between the barrier layer and a sealant layer. In this case, the scavenger layer may be an uncrosslinked plastic or may be a lacquer or adhesive formed, for example, following solvent evaporation, with or without chemical crosslinking, after application to the barrier-forming layer.
In a fifth aspect, the present invention provides a resin for blowmoulding containers such as bottles and jars. said resin comprising an oxygen scavenging composition(s), wherein said oxygen scavenging composition(s) comprise at least one reducible organic compound which is reduced when the composition is subjected to predetermined conditions, the reduced form of the organic compound(s) being oxidisable by ground state molecular oxygen, and wherein the reduction and/or subsequent oxidation of the organic compound(s) occurs independently of each of constant illumination with visible light and the presence of a transition metal catalyst.
Containers manufactured from the resin may be single layer, bilayer or multilayer and the resin would typically comprise, in addition to the oxygen scavenging composition, poly(ethylene terephthalate), PET, poly(ethylene naphthalate), PEN, or blends of these resins or as blends with other polymers such as aromatic polyamides. The use of the oxygen scavenging composition(s) in monolayer bottles and jars is feasible because the oxygen barrier property of plastics like PET is -sufficiently high as to minimise the depletion of the oxygen scavenger to that located near to the outside of the container.
For bilayer and multilayer containers, the resin comprising the oxygen scavenging composition may be used to produce the layer or layers which will be nearest to the contents. The concentration of the reducible organic compound or, where polymerised, the reducible substituent, will preferably exceed that required to initially deoxygenate the contents and any headspace in the container.
In a sixth aspect, the present invention provides an overwrap, shrinkwrap or tight label or coating for use on the outer surface of a container, said overwrap, shrinkwrap or tight label or coating comprising an oxygen scavenging composition(s), wherein said oxygen scavenging composition(s) comprises at least one reducible organic compound which is reduced when the composition is subjected to predetermined conditions, the reduced form of the organic compound(s) being oxidisable by ground state molecular oxygen, and wherein the reduction and/or subsequent oxidation of WO 99/10251 PCT/AU98/00671 9 the organic compound(s) occurs independently of each of constant illumination with visible light and the presence of a transition metal catalyst.
Such an overwrap, shrinkwrap or tight label or coating may be useful for preventing oxygen from permeating a container. The oxygen scavenging composition may be used as the inner layer(s) or as an adhesive of, for instance, a shrink label on a bottle with the outer layer of the shrink label acting as a good oxygen barrier-forming layer. Such wraps or labels need not cover all of the outer surface of the container, depending upon the extent of oxygen permeation barrier required. Thus. the barrier material may be aluminium foil or any oxygen barrier-forming polymer but, preferably, is a polyvinylidene chloride-coated film. a polyamide or a polymer or copolymer of vinyl alcohol, PET or PEN. The barrier mnaterial may also include a layer of aluminium, a metal oxide or carbon, any of which may be deposited by a vacuum technique.
In use an overwrap may take the form of a "Masterpack" which forms a sealed bag or container around several packaged products. These products may be themselves already packaged in an oxygen permeable package so that oxygen released therein can be scavenged by an oxygen scavenging composition layer(s) located on the inside of a Masterpack barrier layer. The Masterpack would normally contain an inert gas atmosphere. Such a pack might be used for extending the shelf life of fresh meat that is already packaged for retail sale or trade use. Alternatively, a Masterpack with an inert gas atmosphere may be used to contain packages which already have a substantial barrier to oxygen but which leak oxygen or allow small amounts of permeation. An example of such a product would be multipacks of pharmaceutical preparations which are very oxygen sensitive.
In a further aspect, the present invention provides a closure liner comprising an oxygen scavenging composition(s), wherein said oxygen scavenging composition(s) comprises at least one reducible organic compound which is reduced when the composition is subjected to predetermined conditions, the reduced form of the organic compound(s) being oxidisable by ground state molecular oxygen, and wherein the reduction and/or subsequent oxidation of the organic compound(s) occurs independently of each of constant illumination with visible light and the presence of a transition metal catalyst.
WO 99/10251 WO 9910251PCT/AU98/00671 Such a l *iner would normally cover most of the inner surface of the closure which contacts the opening of the container and its contents.
Alternatively, the liner could be in the form of an annulus which contacts the opening of the container. Closure liners for oxygen scavenging may be made from any of the polymer or plastisol compositions normally used for such purposes. However, preferably, these polymers will be olefin polymers and copolymers with comonomers which improve properties such as resilience, softness and inertness to the package contents. Plastisols will preferably be made from vinyl chloride polymners and copolymners. Some closures are made from materials, such as plastics. which are partially permeable to oxygen from the air. In such cases it may be necessary to make the oxygen scavenging composition laver an inner layer of a multilayer liner in which an oxygen barrier layer is disposed on the side contacting the closure. In this way the scavenging composition is iot depleted in capacity by oxygen permeating the closure material.
In yet a still further aspect. the present invention provides a can container for foods and liquids, said can including a lacquer, enamel or other polymeric coating comprising an ox 'ygen scavenging composition(s), wherein said oxygen scavenging composition(s) comprises at least one reducible organic compound which is reduced when the composition is subjected to predetermined conditions. the reduced form of the organic compound(s) being oxidisable by ground state molecular oxygen, and wherein the reduction and/or subsequent oxidation of the organic compound(s) occurs independently of each of constant illumination with visible light and the presence of a transition metal catalyst.
The can container may be manufactured from aluminium,. steel and tin-plated steel. The oxygen scavenging composition may be incorporated into the lacquer, enamel or coating by dispersion or blending or, alternatively, one or more of the components of the oxygen scavenging composition may become part of the covalently crosslinked structure if appropriate functional groups are included into their structure. For instance, compounds with the reducible group and containing one or more epoxy groups may be crosslinked into amine-epoxy coatings.
In the present applicant's further copending Australian patent application No. 54896/96 (the entire disclosure of which is incorporated herein by reference), materials comprising the oxygen scavenging WO 99/10251 PCT/AU98/00671 11 compositions contained within oxygen impermeable compartment(s) or microcapsule(s) are described. The compartment(s) or microcapsule(s) of these materials may be broken or otherwise rendered oxygen permeable by application of heat, electromagnetic radiation, mechanical pressure or stress, or by hydration. Thus. these materials permit the oxygen scavenging composition to be "pre-triggered" to the activated state remote from the location at which the material is to be used. It is to be understood that, where appropriate, the oxygen scavenging composition(s) or layer(s) of oxygen scavenging composition(s) described in the packages, applications and products above, may be substituted by a similar oxygen scavenging composition which is in the form of a material as described in patent application No. 54896/96.
The terms "comprise". "comprises" and "comprising" as used throughout the specification are intended to refer to the inclusion of a stated component or feature of group of components of features with or without the inclusion of a further component or feature or group of components or features.
The invention is hereinafter described by way of the following nonlimiting examples and with reference to the accompanying figures.
Brief description of the figures: Figure 1 provides a diagraninatic representation of the mechanism of oxygen scavenging achieved by packages utilising the oxygen scavenging compositions.
Figures 2 to 11 provide schematic representations of embodiments of the packages and applications according to the present invention.
Example 1: Oxygen scavenging (OST) applied to flexible pouches.
An OST film consisted of a blend of a copolymer of ethylene with 9,10anthraquinonyl-2-ethyl acrylate with an anthraquinone content of 18% m/m, and a copolymer of ethylene with dimethylaminopropyl acrylate (31.4 m/m) was produced as follows: WO 99/10251 PCT/AU98/00671 12 Synthesis of copolymer of ethylene and dimethylaminopropylacrylate Apparatus: 5L 4-necked flange flask, mechanical stirrer, Dean-Stark, Condenser, Nitrogen bleed and bubbler.
Lotryl 20MA08 (ATOCHEM, Paris, France, 500g, nominally 20% w/w methyl acrylate units i.e. 1.16 mol) was first dissolved in refluxing toluene 3-Dimethylamino -1-propanol (200ml, 1.62 mol) was then added followed by titanium isopropoxide (6g) as catalyst. The reaction mixture was stirred at reflux for 16 hours with a steady stream of nitrogen over the surface of the reaction mixture. The reaction was monitored by 'H nmr. On completion of the reaction, the reaction mixture was diluted with toluene (2L) before precipitating from an acetone (10L) and toluene (2L) mixture. A fluffy white polymer was obtained which was collected by filtration and washed with acetone The polymer was air dried for 48 hours.
Synthesis of copolymer of ethylene and 9,10-anthraquinonyl 2-ethyl acrylate Preparation of 2-(1-bromoethyl)-anthlraquinone
(BEAQ)
A mixture of 2-ethylanthraquinone (25Kg, 105.9mol), NBS (19.1Kg, 107.3mol) and benzoyl peroxide 200g, 0.58mol) in CCl 4 (-150L) is stirred at reflux for 1.5 hours. On cooling, the precipitate is collected by filtration and washed on the filter with ethanol, hot water and finally ethanol again. After drying, this may be used without further purification (i.e.
recrystallisation from benzene/methanol Reaction of BEAQ with Primacor 3440 Primacor 3440 (Dow Chemical, USA, 20Kg, containing 26.4mol of carboxyl group) is first taken up in refluxing toluene (-120L) followed by the addition of 2-propanol (10L). On allowing the reaction to cool to about 80 oC, DBU (4Kg, 26.3mol) is added. After stirring the reaction mixture for 0.5h at reflux temperature, BEAQ (8Kg, 25.4mol) can be added in portions. The progress of the reaction can be followed by tic analysis (10% EtOAc in WO 99/10251 PCT/AU98/00671 13 Pet.Ether). The reaction is stirred at reflux for 2h., or until no BEAQ can be detected by tic analysis. Acetic acid (7L) is then added, before pouring the reaction mixture onto acetone (200L). The polymer is collected by filtration and washed thoroughly on the filter with acetone, water and finally acetone again.
OST film (25 .m thick) was extruded using a single screw 1 inch extruder with an 35 cm wide slit die onto a PE/EVAL/PE coextrusion substrate. The resulting structure was made into pouches with the OST layer on the inside and separated by a piece of polypropylene film. The pouches had an internal surface area of 700 cm 2 and the weight of OST film used was 1.6 grams. After vacuum sealing, the pouches were irradiated in a commercial UV-curing system emitting at 300 W/inch (Fusion Systems, Maryland, USA) at a conveyor web speed of 10.5 n/min, 10 passes per side of the pouch. One of the pouches had 10 ml oxygen and 490 ml nitrogen injected Pack and the other 15 ml of oxygen and 735 ml nitrogen injected Pack 2 Pouches were stored in darkness at 25 0
C.
The oxygen content of the pouch headspaces was determined periodically by gas chromatography and the results are shown in Table 1.
Tablel: Headspace oxygen in Pouches made using an OST extrusion coating Time hr) Pack 1 Pack 2 oxygen oxygen consumed oxygen oxygen mis consumed mis 0 2.1 0 2.29 0 1.49 3.1 24 1.88 3.13 48 1.29 2.59 72 1.64 4.91 93 1.04 5.36 144 1.55 5.61 168 0.93 5.85 WO 99/10251 PCT/AU98/00671 14 Example2: Oxygen scavenging (OST) applied to Modified Atmosphere Packed Fresh Pasta Laminates comprising the OST film consisted of a web of Barex/OST film/EVA and were formed by heat pressing under pressure. Barex is manufactured by BP Chemicals Ltd. The laminates were then thermoformed into the mould of a Nu-Wave-200 tray Southcorp Packaging, Clayton, Victoria, Australia). Trays were sealed with a lid that consisted of EVOH/OST film/EVA that were formed by heat pressing.
The surface area of a tray was 290 cm 2 the thickness of OST film was The OST film consisted of a blend of a copolymer of ethylene with 9,10-anthraquinonyl-2-ethyl acrylate with an anthraquinone content of 18% m/m, and a copolymer of ethylene with dimethylaminopropyl acrylate (31.4 The trays and lids were then put into pouches made from a PE/EVAL/PE coextrusion. These were vacuum packed and were irradiated in a commercial UV-curing system emitting 300 W/inch (Fusion Systems, Maryland, USA) at a conveyor web speed of 12.6 m/min, 10 times per side.
Trays and lids were removed from their pouches, and trays were filled with 100 grams of fresh pasta, or glass beads (0.5cm diameter). These were then gas flushed with a mixture of 65% CO,. 2% oxygen, 33% nitrogen. The headspace was 200 ml.
Trays were analysed by GC for their gas composition and were stored in darkness at 25 0 C. Controls were handled as above, however they did not contain OST film. The gas analyses over a storage time at 25"C are shown in Table 2.
WO 99/10251 WO 9910251PCT/AU98/0067 1 Table 2: Headspace in OST film trays containing fresh pasta and glass beads Time (hr) OPI 0P2 0 Glass C1 C2 C3 Beads Glass Glass Beads %02 %02 %02 %02 %02 %02 0 2.81 2.31 1.51 5.95 2.25 2.77 1.44 6.42 47 48 1.12 6.46 72 0.96 0.78 0.41 0.73 0.41 141 0.51 2.01 1.8 190 213 0.18 240 282 0.21 360 6.11 note: IndicaHes Ihe, trays xvit Ii OSI'[i H111.1I pm~it 1I S rmi' lailing pasla.
represents contrl Itrays From these results. it can be seen that oxygen is scavenged in trays made using OST film more rapidly than in its absence.
It will be appreciated by persons skilled in the art that numerous variations and/or modifications may be made to the invention as shown in the specific embodiments withouit departing from the spirit or scope of the invention as broadly described. The present emrbodiments are.. therefore, to be considered in all respects as illustrative and not restrictive.
Claims (42)
1. A carton for liquids manufactured from liquid cartonboard comprising one or more layers of an oxygen scavenging composition(s) in combination with at least one gas and vapour barrier-forming layer or coating, wherein said oxygen scavenging composition(s) comprise at least one reducible organic compound which is reduced when the composition is subjected to predetermined conditions, the reduced form of the organic compound(s) being oxidisable by ground state molecular oxygen, and wherein the reduction and/or subsequent oxidisation of the organic compound(s) occurs independently of each of constant illumination with visible light and the presence of a transition metal catalyst.
2. A carton according to claim 1, wherein the said barrier-forming layer or coating is an oxygen barrier-forming layer or coating.
3. A carton according to claim 2, wherein the said barrier-forming layer or coating comprises a layer of aluminium foil or a polymer coated with metal-oxide, polyvinylidene chloride or aluminium. o
4. A carton according to any one of claims 1 to 3, wherein the at least one reducible organic compound is selected from benzoquinone, anthraquinone and napthoquinone.
5. A carton according to any one of claims 1 to 4, wherein the at least one reducible organic compound is selected from 9, 10-anthraquinone and 1,4-napthoquinone. 20
6. A carton according to any one of claims 1 to 5, wherein the at least one reducible organic compound is in a polymerised, copolymerised or oligomerised form.
7. A carton according to any one of claims 1 to 6, wherein the oxygen scavenging component further comprises an activated oxygen scavenging component. i
8. A carton according to claim 7, wherein the activated oxygen scavenging component •25 is selected from antioxidants, amines, organic phosphines, organic phosphites, and sulfur- ooo..: containing compounds.
9. A carton according to any one of claims 1 to 7, wherein the oxygen scavenging 0" 0: composition further comprises a source of labile hydrogen or electrons.
A bag-in-box package for containing liquids including a bag comprising one or more film layers of an oxygen scavenging composition(s) in combination with at least one gas and vapour barrier-forming layer or coating, wherein said oxygen scavenging composition(s) comprises at least one reducible organic compound which is reduced when RA the composition is subjected to predetermined conditions, the reduced form of the organic i _ompound(s) being oxidisable by ground state molecular oxygen, and wherein the 141439105 17 reduction and/or subsequent oxidisation of the organic compound(s) occurs independently of each of constant illumination with visible light and the presence of a transition metal catalyst.
11. A bag-in-box package according to claim 10, wherein the said barrier-forming layer or coating is an oxygen barrier-forming layer or coating.
12. A bag-in-box package according to claim 10 or 11, wherein a tap and tap fitting is affixed to the bag, said tap and/or tap fitting being constructed from a polymer composition comprising an oxygen scavenging composition as defined in claim
13. A bag-in-box package according to any one of claims 10 to 12, wherein the at least one reducible organic compound is selected from benzoquinone, anthraquinone and napthoquinone.
14. A bag-in-box package according to any one of claims 10 to 13, wherein the at least one reducible organic compound is selected from 9, 10-anthraquinone and 1,4- napthoquinone.
15. A bag-in-box package according to any one of claims 10 to 14, wherein the at least one reducible organic compound is in a polymerised, copolymerised or oligomerised form.
16. A bag-in-box package according to any one of claims 1 to 15, wherein the activated oxygen scavenging composition further comprises an activated oxygen scavenging component. 20
17. A bag-in-box package according to claim 16, wherein the activated oxygen scavenging component is selected from antioxidants, amines, organic phosphines, organic phosphites and sulfur-containing compounds.
18. A bag-in-box package according to any one of claims 10 to 17, wherein the oxygen scavenging composition further comprises a source of labile hydrogen or electrons. 25
19. A thermoformed tray, cup or tub comprising an oxygen scavenging composition(s) in combination with at least one gas and vapour barrier-forming layer or coating, wherein said oxygen scavenging composition(s) comprises at least one reducible organic compound which is reduced when the composition is subjected to predetermined conditions, the reduced form of the organic compound(s) being oxidisable by ground state molecular oxygen, and wherein the reduction and/or subsequent oxidation of the organic compound(s) occurs independently of each of constant illumination with visible light and the presence of a transition metal catalyst.
A thermoformed tray, cap or tub according to claim 19, wherein the said barrier- forming layer or coating is an oxygen barrier-forming layer or coating. 141439105 18
21. A thermoformed tray, cup or tub according to claim 20, wherein the oxygen barrier- forming layer or coating comprises a film layer of a high oxygen barrier polymer selected from the group consisting of a polyvinyl alcohol, ethylene vinyl alcohol copolymer and polyvinylidene chloride copolymer.
22. A thermoformed trap, cup or tub according to any one of claims 19 to 21, wherein the at least one reducible organic compound is selected from benzoquinone, anthraquinone and napthoquinone.
23. A thermoformed tray, cup or tub according to any one of claims 19 to 22, wherein the at least one reducible organic compound is selected from 9, 10-anthraquinone and 1,4- napthoquinone.
24. A thermoformed tray, cup or tub according to any one of claims 19 to 23, wherein the at least one reducible organic compound is in a polymerised, copolymerised or oligomerised form.
A thermoformed tray, cup or tub according to any one of claims 19 to 24, wherein the oxygen scavenging composition further comprises an activated oxygen scavenging S component.
26. A thermoformed tray, cup or tub according to claim 25, wherein the activated oxygen scavenging component is selected from antioxidants, amines, organic phosphines, organic phosphites and sulfur-containing compounds. 20
27. A thermoformed tray, cup or tub according to any one of claims 19 to 26, wherein the oxygen scavenging composition further comprises a source of labile hydrogen or electrons.
28. A resin for blow-moulding containers such as bottles and jars, said resin comprising an oxygen scavenging composition(s), wherein said oxygen scavenging composition(s) 25 comprise at least one reducible organic compound which is reduced when the composition is subjected to predetermined conditions, the reduced form of the organic compound(s) being oxidisable by ground state molecular oxygen, and wherein the reduction and/or Ssubsequent oxidation of the organic compound(s) occurs independently of each of constant illumination with visible light and the presence of transition metal catalyst.
29. A resin according to claim 28, further comprising poly(ethylene terephthalate), poly(ethylene napthalate) or blends thereof.
A resin according to claim 28 or 29 wherein the at least one reducible organic compound is selected from benzoquinone, anthraquinone and napthoquinone. 141439105 19
31. A resin according to any one of claims 28 to 30, wherein the at least one reducible organic compound is selected from 9, 10-anthraquinone and 1,4-napthoquinone.
32. A resin according to any of claims 28 to 31, wherein the at least one reducible organic compound is in a polymerised, copolymerised or oligomerised form.
33. A resin according to any one of claims 28 to 32, wherein the oxygen scavenging composition further comprises an activated oxygen scavenging component.
34. A resin according to claim 33, wherein the activated oxygen scavenging component is selected from antioxidants, amines, organic phosphines, organic phosphites and sulfur- containing compounds.
35. A resin according to any one of claims 28 to 34, wherein the oxygen scavenging composition further comprises a source of labile hydrogen or electrons.
36. An overwrap, shrinkwrap or tight label or coating for use on the outer surface of a container, said overwrap, shrinkwrap or tight label or coating comprising an oxygen scavenging composition(s), wherein said oxygen composition(s) comprises at least one reducible organic compound which is reduced when the composition is subjected to 0 predetermined conditions, the reduced form of the organic compound(s) being oxidisable by ground state molecular oxygen and, wherein the reduction and/or subsequent oxidation of the organic compound(s) occur independently of each of constant illumination with visible light and the presence of a transition metal catalyst. 20
37. An overwrap, shrinkwrap or tight label or coating according to claim 36, wherein the at least one reducible organic compound is selected from benzoquinone, anthraquinone and napthoquinone.
38. An overwrap, shrinkwrap or tight label or coating according to claim 36 or 37, wherein the at least one reducible organic compound is selected from 9, 25 and 1,4-napthoquinone. o
39. An overwrap, shrinkwrap or tight label or coating according to any one of claims 36 to 38, wherein the at least one reducible organic compound is in a polymerised, copolymerised or oligomerised form.
40. An overwrap, shrinkwrap or tight label or coating according to any one of claims 36 to 39, wherein the oxygen scavenging composition further comprises an activated oxygen scavenging component.
41. An overwrap, shrinkwrap or tight label or coating according to claim 40, wherein the activated oxygen scavenging component is selected from antioxidants, amines, organic phosphines, organic phosphites and sulfur-containing compounds. 141439105
42. An overwrap, shrinkwrap or tight label or coating according to any one of claims 36 to 40, wherein the oxygen scavenging composition further comprises a source of labile hydrogen or electrons. oo .°oo OoOO ooo oe• *oooo oo o •oaO• ooo oooo
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| AU87230/98A AU758893B2 (en) | 1993-11-24 | 1998-08-21 | New uses for oxygen scavenging compositions |
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| AU55537/94A AU672661C (en) | 1992-11-24 | 1993-11-24 | Oxygen scavengers independent of transition metal catalysts |
| AUPO8684 | 1997-08-21 | ||
| AUPO8684A AUPO868497A0 (en) | 1997-08-21 | 1997-08-21 | New uses for oxygen scavenging compositions |
| AU87230/98A AU758893B2 (en) | 1993-11-24 | 1998-08-21 | New uses for oxygen scavenging compositions |
| PCT/AU1998/000671 WO1999010251A1 (en) | 1997-08-21 | 1998-08-21 | New uses for oxygen scavenging compositions |
Related Parent Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AU55537/94A Addition AU672661C (en) | 1992-11-24 | 1993-11-24 | Oxygen scavengers independent of transition metal catalysts |
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| Publication Number | Publication Date |
|---|---|
| AU8723098A AU8723098A (en) | 1999-03-16 |
| AU758893B2 true AU758893B2 (en) | 2003-04-03 |
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| AU87230/98A Expired AU758893B2 (en) | 1993-11-24 | 1998-08-21 | New uses for oxygen scavenging compositions |
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Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1996034070A1 (en) * | 1995-04-28 | 1996-10-31 | Commonwealth Scientific And Industrial Research Organisation | Triggered active packaging material |
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1998
- 1998-08-21 AU AU87230/98A patent/AU758893B2/en not_active Expired
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1996034070A1 (en) * | 1995-04-28 | 1996-10-31 | Commonwealth Scientific And Industrial Research Organisation | Triggered active packaging material |
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| Publication number | Publication date |
|---|---|
| AU8723098A (en) | 1999-03-16 |
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