AU2012237371B2 - Coating formulation for the interior surfaces of cans - Google Patents
Coating formulation for the interior surfaces of cans Download PDFInfo
- Publication number
- AU2012237371B2 AU2012237371B2 AU2012237371A AU2012237371A AU2012237371B2 AU 2012237371 B2 AU2012237371 B2 AU 2012237371B2 AU 2012237371 A AU2012237371 A AU 2012237371A AU 2012237371 A AU2012237371 A AU 2012237371A AU 2012237371 B2 AU2012237371 B2 AU 2012237371B2
- Authority
- AU
- Australia
- Prior art keywords
- copolymer
- water
- inner coating
- acid
- copolymer mixture
- 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.)
- Ceased
Links
- 239000008199 coating composition Substances 0.000 title description 16
- 229920001577 copolymer Polymers 0.000 claims abstract description 153
- 238000000576 coating method Methods 0.000 claims abstract description 133
- 239000011248 coating agent Substances 0.000 claims abstract description 111
- 239000000203 mixture Substances 0.000 claims abstract description 91
- 239000002253 acid Substances 0.000 claims abstract description 39
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 30
- -1 acyclic alkene Chemical class 0.000 claims abstract description 26
- 125000001931 aliphatic group Chemical group 0.000 claims abstract description 17
- 150000001718 carbodiimides Chemical class 0.000 claims abstract description 14
- 229920003180 amino resin Polymers 0.000 claims abstract description 7
- 239000003795 chemical substances by application Substances 0.000 claims description 27
- 150000001735 carboxylic acids Chemical class 0.000 claims description 20
- 238000000034 method Methods 0.000 claims description 16
- 230000008569 process Effects 0.000 claims description 15
- 239000000470 constituent Substances 0.000 claims description 13
- 239000000159 acid neutralizing agent Substances 0.000 claims description 12
- 239000003995 emulsifying agent Substances 0.000 claims description 12
- 239000005028 tinplate Substances 0.000 claims description 12
- 239000007921 spray Substances 0.000 claims description 10
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 9
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims description 8
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 8
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims description 8
- 229910052782 aluminium Inorganic materials 0.000 claims description 8
- 239000003960 organic solvent Substances 0.000 claims description 8
- 150000001412 amines Chemical class 0.000 claims description 7
- 150000002148 esters Chemical class 0.000 claims description 7
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims description 6
- 230000003472 neutralizing effect Effects 0.000 claims description 6
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 claims description 4
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 claims description 4
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical group C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 4
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 claims description 4
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 claims description 4
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical compound CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 claims description 4
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 claims description 4
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 claims description 4
- 229910021529 ammonia Inorganic materials 0.000 claims description 4
- IAQRGUVFOMOMEM-UHFFFAOYSA-N but-2-ene Chemical compound CC=CC IAQRGUVFOMOMEM-UHFFFAOYSA-N 0.000 claims description 4
- 125000004432 carbon atom Chemical group C* 0.000 claims description 4
- 239000003054 catalyst Substances 0.000 claims description 4
- 230000009477 glass transition Effects 0.000 claims description 4
- 239000003381 stabilizer Substances 0.000 claims description 4
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 claims description 4
- 239000000080 wetting agent Substances 0.000 claims description 4
- 150000004679 hydroxides Chemical class 0.000 claims description 3
- 229910052725 zinc Inorganic materials 0.000 claims description 3
- WBYWAXJHAXSJNI-VOTSOKGWSA-M .beta-Phenylacrylic acid Natural products [O-]C(=O)\C=C\C1=CC=CC=C1 WBYWAXJHAXSJNI-VOTSOKGWSA-M 0.000 claims description 2
- JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 claims description 2
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 claims description 2
- BFSVOASYOCHEOV-UHFFFAOYSA-N 2-diethylaminoethanol Chemical compound CCN(CC)CCO BFSVOASYOCHEOV-UHFFFAOYSA-N 0.000 claims description 2
- WBYWAXJHAXSJNI-SREVYHEPSA-N Cinnamic acid Chemical compound OC(=O)\C=C/C1=CC=CC=C1 WBYWAXJHAXSJNI-SREVYHEPSA-N 0.000 claims description 2
- AVXURJPOCDRRFD-UHFFFAOYSA-N Hydroxylamine Chemical compound ON AVXURJPOCDRRFD-UHFFFAOYSA-N 0.000 claims description 2
- UEEJHVSXFDXPFK-UHFFFAOYSA-N N-dimethylaminoethanol Chemical compound CN(C)CCO UEEJHVSXFDXPFK-UHFFFAOYSA-N 0.000 claims description 2
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims description 2
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 claims description 2
- 125000005907 alkyl ester group Chemical group 0.000 claims description 2
- 229910052791 calcium Inorganic materials 0.000 claims description 2
- 229930016911 cinnamic acid Natural products 0.000 claims description 2
- 235000013985 cinnamic acid Nutrition 0.000 claims description 2
- LDHQCZJRKDOVOX-NSCUHMNNSA-N crotonic acid Chemical compound C\C=C\C(O)=O LDHQCZJRKDOVOX-NSCUHMNNSA-N 0.000 claims description 2
- 229960002887 deanol Drugs 0.000 claims description 2
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 claims description 2
- XNMQEEKYCVKGBD-UHFFFAOYSA-N dimethylacetylene Natural products CC#CC XNMQEEKYCVKGBD-UHFFFAOYSA-N 0.000 claims description 2
- 239000012972 dimethylethanolamine Substances 0.000 claims description 2
- 239000001530 fumaric acid Substances 0.000 claims description 2
- 229910052742 iron Inorganic materials 0.000 claims description 2
- 229910052744 lithium Inorganic materials 0.000 claims description 2
- 229910052749 magnesium Inorganic materials 0.000 claims description 2
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 claims description 2
- 239000011976 maleic acid Substances 0.000 claims description 2
- WBYWAXJHAXSJNI-UHFFFAOYSA-N methyl p-hydroxycinnamate Natural products OC(=O)C=CC1=CC=CC=C1 WBYWAXJHAXSJNI-UHFFFAOYSA-N 0.000 claims description 2
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 claims description 2
- 229910052700 potassium Inorganic materials 0.000 claims description 2
- 229910052708 sodium Inorganic materials 0.000 claims description 2
- LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 claims description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 claims 2
- 239000001294 propane Substances 0.000 claims 1
- 150000002118 epoxides Chemical class 0.000 abstract description 13
- 238000004132 cross linking Methods 0.000 abstract description 8
- 239000007788 liquid Substances 0.000 abstract description 7
- 229930185605 Bisphenol Natural products 0.000 abstract description 3
- VPWNQTHUCYMVMZ-UHFFFAOYSA-N 4,4'-sulfonyldiphenol Chemical class C1=CC(O)=CC=C1S(=O)(=O)C1=CC=C(O)C=C1 VPWNQTHUCYMVMZ-UHFFFAOYSA-N 0.000 abstract description 2
- 238000005299 abrasion Methods 0.000 abstract description 2
- 239000004848 polyfunctional curative Substances 0.000 abstract 2
- 150000004649 carbonic acid derivatives Chemical class 0.000 abstract 1
- 239000010408 film Substances 0.000 description 28
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 18
- 238000009472 formulation Methods 0.000 description 10
- 239000008346 aqueous phase Substances 0.000 description 9
- 235000013361 beverage Nutrition 0.000 description 7
- 229910052751 metal Inorganic materials 0.000 description 7
- 239000002184 metal Substances 0.000 description 7
- 238000006386 neutralization reaction Methods 0.000 description 7
- 239000002904 solvent Substances 0.000 description 7
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- 239000000463 material Substances 0.000 description 6
- 239000002245 particle Substances 0.000 description 5
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 4
- 150000001336 alkenes Chemical class 0.000 description 4
- 230000004888 barrier function Effects 0.000 description 4
- 125000005442 diisocyanate group Chemical group 0.000 description 4
- 239000006185 dispersion Substances 0.000 description 4
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- 238000004806 packaging method and process Methods 0.000 description 4
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- 229920000877 Melamine resin Polymers 0.000 description 3
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 3
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 3
- 239000012736 aqueous medium Substances 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- RAABOESOVLLHRU-UHFFFAOYSA-N diazene Chemical group N=N RAABOESOVLLHRU-UHFFFAOYSA-N 0.000 description 3
- 239000003822 epoxy resin Substances 0.000 description 3
- 238000011049 filling Methods 0.000 description 3
- 235000013305 food Nutrition 0.000 description 3
- 229920000647 polyepoxide Polymers 0.000 description 3
- ZRALSGWEFCBTJO-UHFFFAOYSA-N Guanidine Chemical compound NC(N)=N ZRALSGWEFCBTJO-UHFFFAOYSA-N 0.000 description 2
- QQONPFPTGQHPMA-UHFFFAOYSA-N Propene Chemical compound CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 2
- 125000002723 alicyclic group Chemical group 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- 239000002585 base Substances 0.000 description 2
- 238000006482 condensation reaction Methods 0.000 description 2
- 238000005260 corrosion Methods 0.000 description 2
- 230000007797 corrosion Effects 0.000 description 2
- 238000006114 decarboxylation reaction Methods 0.000 description 2
- OGQYPPBGSLZBEG-UHFFFAOYSA-N dimethyl(dioctadecyl)azanium Chemical compound CCCCCCCCCCCCCCCCCC[N+](C)(C)CCCCCCCCCCCCCCCCCC OGQYPPBGSLZBEG-UHFFFAOYSA-N 0.000 description 2
- 238000009826 distribution Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000004945 emulsification Methods 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 125000004435 hydrogen atom Chemical class [H]* 0.000 description 2
- 229920000126 latex Polymers 0.000 description 2
- 239000010410 layer Substances 0.000 description 2
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 2
- 239000000178 monomer Substances 0.000 description 2
- 229920000620 organic polymer Polymers 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 125000006239 protecting group Chemical group 0.000 description 2
- 239000011241 protective layer Substances 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000007858 starting material Substances 0.000 description 2
- 239000010409 thin film Substances 0.000 description 2
- 239000011701 zinc Substances 0.000 description 2
- NNOZGCICXAYKLW-UHFFFAOYSA-N 1,2-bis(2-isocyanatopropan-2-yl)benzene Chemical compound O=C=NC(C)(C)C1=CC=CC=C1C(C)(C)N=C=O NNOZGCICXAYKLW-UHFFFAOYSA-N 0.000 description 1
- FKTHNVSLHLHISI-UHFFFAOYSA-N 1,2-bis(isocyanatomethyl)benzene Chemical compound O=C=NCC1=CC=CC=C1CN=C=O FKTHNVSLHLHISI-UHFFFAOYSA-N 0.000 description 1
- VGHSXKTVMPXHNG-UHFFFAOYSA-N 1,3-diisocyanatobenzene Chemical compound O=C=NC1=CC=CC(N=C=O)=C1 VGHSXKTVMPXHNG-UHFFFAOYSA-N 0.000 description 1
- ALQLPWJFHRMHIU-UHFFFAOYSA-N 1,4-diisocyanatobenzene Chemical compound O=C=NC1=CC=C(N=C=O)C=C1 ALQLPWJFHRMHIU-UHFFFAOYSA-N 0.000 description 1
- CDMDQYCEEKCBGR-UHFFFAOYSA-N 1,4-diisocyanatocyclohexane Chemical compound O=C=NC1CCC(N=C=O)CC1 CDMDQYCEEKCBGR-UHFFFAOYSA-N 0.000 description 1
- SBJCUZQNHOLYMD-UHFFFAOYSA-N 1,5-Naphthalene diisocyanate Chemical compound C1=CC=C2C(N=C=O)=CC=CC2=C1N=C=O SBJCUZQNHOLYMD-UHFFFAOYSA-N 0.000 description 1
- UPMLOUAZCHDJJD-UHFFFAOYSA-N 4,4'-Diphenylmethane Diisocyanate Chemical compound C1=CC(N=C=O)=CC=C1CC1=CC=C(N=C=O)C=C1 UPMLOUAZCHDJJD-UHFFFAOYSA-N 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- 239000005057 Hexamethylene diisocyanate Substances 0.000 description 1
- 239000005058 Isophorone diisocyanate Substances 0.000 description 1
- CHJJGSNFBQVOTG-UHFFFAOYSA-N N-methyl-guanidine Natural products CNC(N)=N CHJJGSNFBQVOTG-UHFFFAOYSA-N 0.000 description 1
- HDONYZHVZVCMLR-UHFFFAOYSA-N N=C=O.N=C=O.CC1CCCCC1 Chemical compound N=C=O.N=C=O.CC1CCCCC1 HDONYZHVZVCMLR-UHFFFAOYSA-N 0.000 description 1
- 229910002651 NO3 Inorganic materials 0.000 description 1
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 1
- 150000001342 alkaline earth metals Chemical class 0.000 description 1
- 159000000013 aluminium salts Chemical class 0.000 description 1
- 239000013011 aqueous formulation Substances 0.000 description 1
- 238000000149 argon plasma sintering Methods 0.000 description 1
- 238000000889 atomisation Methods 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000011247 coating layer Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 230000001186 cumulative effect Effects 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 229910000071 diazene Inorganic materials 0.000 description 1
- QGBSISYHAICWAH-UHFFFAOYSA-N dicyandiamide Chemical compound NC(N)=NC#N QGBSISYHAICWAH-UHFFFAOYSA-N 0.000 description 1
- SWSQBOPZIKWTGO-UHFFFAOYSA-N dimethylaminoamidine Natural products CN(C)C(N)=N SWSQBOPZIKWTGO-UHFFFAOYSA-N 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000003792 electrolyte Substances 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 229940011871 estrogen Drugs 0.000 description 1
- 239000000262 estrogen Substances 0.000 description 1
- 229920001002 functional polymer Polymers 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 1
- 230000036541 health Effects 0.000 description 1
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 1
- 239000008240 homogeneous mixture Substances 0.000 description 1
- 238000000265 homogenisation Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 125000002768 hydroxyalkyl group Chemical group 0.000 description 1
- 230000010220 ion permeability Effects 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 239000012948 isocyanate Substances 0.000 description 1
- 150000002513 isocyanates Chemical class 0.000 description 1
- NIMLQBUJDJZYEJ-UHFFFAOYSA-N isophorone diisocyanate Chemical compound CC1(C)CC(N=C=O)CC(C)(CN=C=O)C1 NIMLQBUJDJZYEJ-UHFFFAOYSA-N 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 239000007769 metal material Substances 0.000 description 1
- 230000005012 migration Effects 0.000 description 1
- 238000013508 migration Methods 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 239000012071 phase Substances 0.000 description 1
- 235000011007 phosphoric acid Nutrition 0.000 description 1
- 229920001515 polyalkylene glycol Polymers 0.000 description 1
- 238000003918 potentiometric titration Methods 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 235000013324 preserved food Nutrition 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000011877 solvent mixture Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- 231100000462 teratogen Toxicity 0.000 description 1
- 239000003439 teratogenic agent Substances 0.000 description 1
- HWCKGOZZJDHMNC-UHFFFAOYSA-M tetraethylammonium bromide Chemical compound [Br-].CC[N+](CC)(CC)CC HWCKGOZZJDHMNC-UHFFFAOYSA-M 0.000 description 1
- 230000009974 thixotropic effect Effects 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
Classifications
-
- 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
- B65D25/00—Details of other kinds or types of rigid or semi-rigid containers
- B65D25/14—Linings or internal coatings
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D123/00—Coating compositions based on homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Coating compositions based on derivatives of such polymers
- C09D123/02—Coating compositions based on homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Coating compositions based on derivatives of such polymers not modified by chemical after-treatment
- C09D123/04—Homopolymers or copolymers of ethene
- C09D123/08—Copolymers of ethene
- C09D123/0846—Copolymers of ethene with unsaturated hydrocarbons containing other atoms than carbon or hydrogen atoms
- C09D123/0869—Acids or derivatives thereof
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Life Sciences & Earth Sciences (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Mechanical Engineering (AREA)
- Paints Or Removers (AREA)
- Application Of Or Painting With Fluid Materials (AREA)
- Details Of Rigid Or Semi-Rigid Containers (AREA)
Abstract
The invention relates to a water-based can interior coating comprising a copolymer or a copolymer mixture at least of an aliphatic and acyclic alkene having at least one α,β-unsaturated carbonic acid in water-dispersed form, wherein the acid count of the copolymer or the copolymer mixture is at least 20 mg KOH / g, but not more than 200 mg KOH / g, and at least one water-dispersed or water-soluble hardener selected from the group of aminoplasts and/or the group of carbodiimides. Can interior coatings according to the invention are characterized in that, as a hardened film, said coatings have exceptional properties with respect to hardness, abrasion resistance and resistance to hot liquids due to the good cross linking of the copolymer or the copolymer mixture with the hardener on the interior surfaces of metallic cans. The invention offers an alternative to the conventional use of epoxides based on bisphenols in can interior coatings.
Description
1 COATING FORMULATION FOR THE INTERIOR SURFACES OF CANS [0002]The present invention relates to a water-based can inner coating comprising a copolymer or a copolymer mixture of at least one aliphatic and acyclic alkene with at least one a4p-unsaturated carboxylic acid in water dispersed form, wherein the acid number of the copolymer or of the copolymer mixture is at least 20 mg KOH / g, but not more than 200 mg KOH / g, and at least one water-dispersed or water-soluble curing agent selected from the group of aminoplasts and/or the group of carbodilmides, Inventive can inner coatings are characterized in that due to the good crosslinking of the copolymer or of the copolymer mixture with the curing agent, the cured film on the inner surfaces of metal cans possesses excellent properties in regard to hardness, abrasion resistance and resistance towards aqueous liquids. The present invention makes available an alternative to the conventional use of epoxides based on bisphenols in can Inner coatings. [00031 In the food industry, tin plate strip is valued as a suitable material for the production of packaging units for receiving aqueous liquids or preserved foods. This is because, even over a longer period of time, tin plate strip, due to its electrochemically noble tin layer, releases only low amounts of potentially toxic tin salts to the food product that is in contact with the tin surface. Tin plate strip is therefore an important starting material for food packaging, for example for the production of cans for receiving beverages. Aluminum strip, due to Its passive oxide layer, is also a suitable starting material for the production of cans for filling with beverages. In addition, aluminium salts that are taken up in small amounts by the liquid are harmless to health. [0004]The packaging industry, when producing cans, coats the Inner surface of the can with an organic protective layer or alternatively uses a strip material pre-coated with an organic protective layer for producing cans. The organic finish that coats the inner surface prevents any direct contact of the metallic interior of the can with the liquid. This achieves first of all a significantly reduced corrosion of the base material and secondly minimizes the entry of metal salts, H 09098 PCT such that the taste of the foodstuff is not changed for the worse even after a lengthy storage or stockpiling of the beverage cans. [0005]Another aspect in regard to the production of cans concerns the composition of the coating, which conventionally consists of epoxy resins based on Bisphenol A. Such epoxides with a Bisphenol A basic structure are suspected estrogens and are teratogens for males. Cured coating formulations that come into contact with acid-containing aqueous foodstuffs can release Bisphenol A from the coating into the stored foodstuff. In practice, the curing of the coating and the resulting crosslinking of the coating components is also never complete, such that unreacted Bisphenol A-based epoxides can also diffuse into the foodstuff. Consequently there exists a need for Bisphenol A-free formulations for the inner coating of cans for storing foodstuffs; various national legislation initiatives, driven inter alia by the EU Directive 2002/72/EU, exist that define the maximum limits for the migration of Bisphenol A from packaging into foodstuffs. [0006] US 2008/0193689 discloses an epoxide-based coating composition that is suitable for use as a can coating and comprises, in addition to the epoxy resin, mono and difunctional low molecular weight organic compounds that can react with the epoxy resin. The coating is formulated in such a way that after curing, only very minor amounts of unreacted epoxides based on Bisphenol A remain in the coating, such that when the composition is used as a can inner coating only traces of Bisphenol A from the cured coating can migrate into the stored foodstuff. [0007]On the other hand, EP 2031006 proposes can inner coatings based on specific alicyclic epoxides, so as to circumvent in this way the formulations that include epoxides based on Bisphenol A. [0008]WO 2006/045017 provides a beverage can coating formulation that contains latices of ethylenically unsaturated monomers and an aqueous dispersion of an acid-functional polymer in the presence of amines, wherein the latices for the crosslinking are constructed at least partially from monomers 2 3 having a gylcidyl group. Such can inner coatings can be formulated free of epoxides based on Bisphenol A. [0009] The object of the present invention consists in providing another alternative to an epoxide-based can inner coating, wherein the coating formulation can be deposited on the inner surfaces of the can in a spray process and after curing affords thin, homogeneous, highly flexible coating films with a simultaneously good coating adhesion and resistance towards aqueous compositions. Another object consists in being able as far as possible to obviate the use of organic solvents and emulsifiers in the formulation of stable and coatable can inner coatings. [0010] According to a first aspect of the present invention, there is provided a water-based can inner coating comprising, in addition to water, a) a copolymer or a copolymer mixture of at least one aliphatic and acyclic alkene with at least one a,p-unsaturated carboxylic acid and at least one ester of as-unsaturated carboxylic acids in water dispersed form, wherein the acid number of the copolymer or of the copolymer mixture is at least 20 mg KOH/g, but less than 100 mg KOH/g, and b) at least one water-dispersed or water-soluble curing agent selected from the group of aminoplasts and/or the group of carbodiimides. [001 Oa] According to a second aspect of the present invention, there is provided use of a copolymer or a copolymer mixture of at least one aliphatic and acyclic alkene with at least one a,@-unsaturated carboxylic acid and at least one ester of a,$-unsaturated carboxylic acids in water-dispersed form, wherein the acid number of the copolymer or of the copolymer mixture is at least 20 mg KOH/g, but less than 100 mg KOH/g, and the acid groups of the copolymer or of the copolymer mixture in the water-dispersed form are at least 20%, but not more than 70% neutralized, as a constituent of the water-based can inner coating. [0010b] According to a third aspect of the present invention, there is provided use of a can inner coating according to the first aspect, wherein the inner coating is deposited in a dry film thickness of at least 5 g/m 2 , but preferably in a dry film thickness of not more than 50 g/m 2 , on to the inner surface of a tin plate can. [001Oc] Use of a can inner coating according to the first aspect, wherein the inner coating is deposited in a dry film thickness of at least 1.5 g/m 2 , but preferably in a dry film thickness of not more than 50 g/m 2 , on to the inner surface of an aluminum can.
3a [1011] Cans are inventively understood to mean metallic containers for filling, storing and holding stocks of foodstuffs, in particular of beverages. [0012] In this context, a can inner coating is a coating formulation that for the formation of a coating layer on the inner surface of the can is deposited, made into a film and cured in order to prevent the direct contact of the foodstuff with the metallic material of the can during filling, storing and holding stocks of the foodstuff. [0013]A water-based coating inventively contains a dispersion and/or emulsion of organic polymers in a continuous aqueous phase, wherein in the context of the present invention, an aqueous phase is also understood to mean a homogeneous mixture of water and a water-miscible solvent. The term "in H 09098 PCT water-dispersed form" therefore means that each polymer is dispersed as a solid or liquid in the continuous aqueous phase. [0014]According to the invention, mixtures of chemically and/or structurally different copolymers of at least one aliphatic and acyclic alkene with at least one a,p-unsaturated carboxylic acid constitute a copolymer mixture. Thus, a copolymer mixture of an inventive coating formulation, can for example comprise in parallel copolymers that comprise different alkenes or different a,p unsaturated carboxylic acids as the comonomers or have a different number of otherwise identical comonomers in the copolymer. [0015]The acid number is inventively an experimentally measurable characteristic number that reflects the number of the free acid groups in the copolymer or in the copolymer mixture. [0016]The acid number is determined by dissolving a weighed quantity of the copolymer or the copolymer mixture in a solvent mixture of methanol and distilled water in the volume ratio 3: 1, and subsequently potentiometrically titrating the mixture with 0.05 mol/ KOH in methanol. The potentiometric measurement is carried out with a combination electrode (LL-Solvotrode@ from Metrohm; reference electrolyte: 0.4 mol/1 tetraethylammonium bromide in ethylene glycol). Here, the acid number corresponds to the added quantity of KOH in milligrams per gram copolymer or copolymer mixture at the inflection point of the potentiometric titration curve. [0017]As a melted on, thin film on metal surfaces the copolymer or copolymer mixture of the aliphatic and acyclic alkane with an a,p-unsaturated carboxylic acid with the abovementioned acid number already shows a good coating adhesion, in particular on tin plate and aluminum surfaces. In addition, the acid groups impart the inherent characteristic to the copolymer or to the copolymer mixture of being self-emulsifying, such that in the aqueous phase, even in the absence of emulsifiers, microparticulate aggregates can be formed by using shear forces. The presence of the copolymer or copolymer mixture in the form of a microparticulate aggregate lends thixotropic properties to the inventive coating, such that a homogeneous wet film of the water-based coating can be 4 H 09098 PCT deposited onto the inner surface of the can, the coating remaining there until a film is formed and cured, and does not run off inside the can due to the force of gravity. [0018] If the acid number of the copolymer or copolymer mixture of alkenes and a,p-unsaturated carboxylic acids is less than 20 mg KOH / g, then a cured coating formulation according to the art of the present invention does not have sufficient adhesion to metal surfaces and consequently is not suitable as a film forming component of can inner coatings. Conversely, an acid number of the copolymer or copolymer mixture of alkenes and a,p-unsaturated carboxylic acids greater than 200 mg KOH / g as the film-forming component in can inner coatings only brings about an inadequate barrier effect against corrosively acting ions in aqueous media and furthermore a coating that is comparatively less resistant against water at temperatures above 60 0 C. [0019]The weight fraction of the aliphatic and acyclic alkenes in the copolymer or in the copolymer mixture is preferably at least 40 wt %, particularly preferably at least 60 wt %, but preferably not more than 95 wt %. This ensures that the ion-permeability of the cured coating on the can inner surface and the swelling of the coating in contact with aqueous media, with at the same time an adequate wettability and adhesion of the coating to the material of the can, is reduced as much as possible. [0020] Preferred aliphatic and acyclic alkenes of the inventively obtained copolymer or copolymer mixture are selected from ethene, propene, 1-butene, 2-butene, isobutene, 1,3-butadiene and/or 2-methylbuta-1,3-diene, particularly preferably ethene. [0021]Preferred a,p-unsaturated carboxylic acids of the inventively obtained copolymer or copolymer mixture are selected from cinnamic acid, crotonic acid, fumaric acid, itaconic acid, maleic acid, acrylic acid and/or methacrylic acid, particularly preferably acrylic acid and/or methacrylic acid, in particular acrylic acid. 5 H 09098 PCT [0022]Further comonomers that may be an additional component of the copolymer or the copolymer mixture in an inventive can inner coating are selected from esters of a,@-unsaturated carboxylic acids, preferably linear or branched alkyl esters of the acrylic acid and/or methacrylic acid containing not more than 12 carbon atoms in the aliphatic group. Such comonomers improve the adhesion of the cured inner coating of the can to metal surfaces due to an increased mobility of the polymer backbone which again facilitates the orientation of the acid groups that have a surface affinity to the metal surface. This effect is ensured in particular with low acid numbers of the copolymer below 100 mg KOH / g. It is generally the case that low acid numbers of the copolymer or copolymer mixture improve the barrier properties of the cured inventive coating formulation when exposed to aqueous media. Accordingly, copolymers or copolymer mixtures that additionally comprise the above described comonomers are inventively preferred with acid numbers below 100 mg KOH / g, particularly below 60 mg KOH / g. [0023]The copolymer or the copolymer mixture of the inventive can inner coating preferably comprises less than 0.05 wt %, particularly preferably less than 0.01 wt %, of epoxidically bonded oxygen. [0024]A good film-formation when curing the can inner coating requires that the water-dispersed copolymer or the water-dispersed copolymer mixture of the can inner coating is converted into a melted state after the aqueous phase has been driven off. This requirement is satisfied when copolymers or copolymer mixtures are preferred that as such have a glass transition temperature of not more than 80 *C, particularly preferably not more than 60 *C. Copolymers or copolymer mixtures with a weight average molecular weight Mw of not more than 20 000 u and which are based on alkenes and a,p-unsaturated carboxylic acids usually have glass transition temperatures that are significantly below 100 0C, such that copolymers or copolymer mixtures with a weight average molecular weight of not more than 20 000 u, in particular not more than 15 000 u, are preferred in inventive can inner coatings. 6 H 09098 PCT [0025] In a preferred formulation of the inventive can inner coating, the acid groups of the water-dispersed copolymer or the water-dispersed copolymer mixture are at least partially neutralized. This measure increases the ability of the copolymer for self-emulsification in the aqueous phase, such that more stable coating formulations result with lower particle sizes of the dispersed copolymers. Accordingly, the can inner coating preferably additionally comprises a neutralizing agent. Preferred suitable neutralization agents that are additionally comprised in such a preferred formulation are ammonia, amines, metallic aluminum and/or zinc, preferably in powdered form, as well as water soluble oxides and hydroxides of the elements Li, Na, K, Mg, Ca, Fe(ll) and Sn(II). The person skilled in the art is aware here that the neutralization agents, corresponding to their function, enter into neutralization reactions with the components of the inventive coating, and therefore in these preferred formulations are optionally detectable as such only indirectly in the form of their reaction products. For example, metallic aluminum powder or zinc powder reacts in the aqueous phase, giving off hydrogen, to afford the corresponding hydroxides that again neutralize the acid groups of the copolymer or copolymer mixture, such that in the inventive coating finally only the cations of the elements aluminum or zinc can be detected. The neutralization agents are therefore understood to be solely as formulation aids of the inventive can inner coating. Ammonia and amines are particularly preferred neutralization agents, as they pass into the gas phase when the coating is cured at elevated temperatures and therefore do not remain in the cured can inner coating. Preferred amines that can be employed as the neutralization agent in inventive can inner coatings are morpholine, hydrazine, hydroxylamine, monoethanolamine, diethanolamine, triethanolamine, dimethylethanolamine and/or diethylethanolamine. [0026]The degree of neutralization of the acid groups in the copolymer or copolymer mixture in the inventive can inner coating is such that at least 20%, particularly preferably at least 30% of the acid groups are neutralized. High degrees of neutralization above 70%, preferably above 60%, are to be avoided in a preferred embodiment of the can inner coating, as the almost completely 7 H 09098 PCT neutralized copolymers are already dissolved in significant amounts in water, thereby resulting again in a high viscosity of the coating and average particle sizes of the dispersed copolymer or copolymer mixture in the sub-micrometer range, such that these kinds of formulations are less suitable as the can inner coating due to their rheological properties. [0027]In this context, the neutralization agent to the can inner coating is preferably to be formulated in such an amount that, based on 1 g of copolymer or copolymer mixture, at least 4/z pmol, preferably at least 6/z pmol, each multiplied by the acid number of the copolymer or copolymer mixture, are comprised as the neutralization agent, but preferably not more than 12/z pmol, particularly not more than 10/z pmol, multiplied by the acid number of the copolymer or copolymer mixture. The divisor z is a natural number and corresponds to the equivalent number of the neutralization reaction. The equivalent number represents how many moles of acid groups of the copolymer or copolymer mixture are neutralized by one mole of the neutralization agent. [0028]The inventive can inner coating comprises a water-dispersed or water soluble curing agent from the group of aminoplasts and/or the group of carbodiimides. The curing agent enables the copolymer or the copolymer mixture to crosslink in a condensation reaction and thus to form a cured coating film on the inner surface of the can. The barrier properties of the cured inventive can inner coating as a film are comparable with those of cured epoxide-based coating films. [0029] In the inventive coating the curing agent must have the characteristic that it crosslinks the copolymer or copolymer mixture through a condensation reaction only at temperatures above the glass transition temperature, preferably only above 100 "C, as otherwise, curing would already occur before the dispersed polymeric components of the coating could form a complete film on the inner surface of the can, thus producing very heterogeneous coating films. 8 H 09098 PCT [0030] Particularly suitable aminoplast curing agents are based on melamine, urea, dicyandiamide, guanamines and/or guanidine. In inventive can inner coatings, the aminoplast curing agents are particularly preferably melamine formaldehyde resins with a molar ratio of formaldehyde: melamine that is preferably greater than 1.5. [0031]Alternatively or in addition, the curing agent of the inventive can inner coating is a carbodiimide. According to the invention, carbodiimides possess at least one diimide structural moiety of the -C=N=C- type. However, they are preferably polyfunctional with a diimide equivalent weight in the range of 300 500 grams of the polyfunctional compound per mole of diimide groups. Particularly preferred carbodiimides result from isocyanates with at least two isocyanate groups by decarboxylation, in particular those of the general Formula (1): OCiN-R, m N-R4NCmO () with n: a whole natural number between 1 and 20;
R
1 an aromatic, aliphatic or alicyclic residue with not more than 16 carbon atoms. [0032]The isocyanate groups are additionally preferably blocked with hydrophilic protective groups that as such lend an improved water-dispersibility or water-solubility to the carbodiimide. The use of these preferred carbodiimides furnishes the additional advantage that the can inner coating can be formulated to be almost free of organic solvents as these carbodiimides are highly water-soluble without already crosslinking the copolymer or copolymer mixture in the aqueous formulation. In a preferred embodiment of an inventive can inner coating that at least partially comprises carbodiimides as the curing agent, the content of organic solvents is therefore less than 10 wt %, particularly preferably less than 4 wt %, in particular the can inner coating preferably comprises no solvent. Exemplary suitable protective groups with hydrophilic character are hydroxyalkyl sulfonic acids, hydroxyalkyl phosphonic 9 H 09098 PCT acids, hydroxyalkyl phosphoric acids, polyalkylene glycols as well as quaternary aminoalkyl alcohols and aminoalkylamines. In a particularly preferred embodiment of the can inner coating, the curing agent is therefore selected from carbodiimides with blocked terminal isocyanate groups according to the general structural Formula (11): X-i-N-R4--C==N-R]N- X 0 110 with n: a whole natural number between 1 and 20;
R
1 : an aromatic, aliphatic or alicyclic residue with not more than 16 carbon atoms. X: -NH-R 1
-N(R
1
)
2 , -O-R 1
-N(R
1
)
2 , -NH-Ri-N(R 1
)
3 Y, -O-R 1
-N(R
1
)
3 Y,
-O-R
1
-SO
3 Z, -O-R 1
-O-PO
3 Z, -O-R 1
-PO
3 Z, -O-(C 2
H
4 )p-OH,
-O-(C
3
H
6 )p-OH with Y: hydroxide, chloride, nitrate, sulfate with Z: hydrogen, ammonium, alkali metal or alkaline earth metal with p: a whole natural number between 1 and 6 [0033] Preferred diisocyanates that are afforded by decarboxylation of the corresponding carbodiimides are for example hexamethylene diisocyanate, cyclohexane-1,4-diisocyanate, xylylene diisocyanate, isophorone diisocyanate, d icyclohexylmethane-4,4-diisocyanate, methylcyclohexane diisocyanate and tetramethylxylylene diisocyanate, 1,5-naphthylene diisocyanate, 4,4 diphenylmethane diisocyanate, 4,4-diphenyldimethylmethane diisocyanate, 1,3 phenylene diisocyanate, 1,4-phenylene diisocyanate, 2,4-toluenylene diisocyanate, 2,6-toluenylene diisocyanate. [0034] Basically, the weight average molecular weight M, of the curing agent in the inventive can inner coating is preferably not more than 2500 u, particularly 10 H 09098 PCT preferably not more than 1500 u, in order to ensure an adequate crosslinking with the copolymer or the copolymer mixture. [0035]The flow properties of the inventive can inner coating are preferably to be adjusted, such that on the one hand to enable the coating to be applied in a spray process and especially in the airless process (which illustrates an airless atomization spray process) that is usually used in the beverage can industry. On the other hand, the wet film deposited on the inner surface of the can must not immediately run off due to gravitational forces, thereby causing an inhomogeneous coating. Optimum flow properties with good film formation of the dispersed constituents are obtained for inventive can coatings, whose dispersed polymeric constituents of the water-based coating preferably have a
D
90 value of not more than 100 pm, particularly preferably not more than 60 pm, wherein the D 50 value is preferably not less than 1 pm, particularly preferably not less than 10 pm. The Do-value, respectively the D 50 -value, means that 90 vol % respectively 50 vol % of the dispersed particles of the can inner coating are smaller than the specified value. [0036]The D 9 o-value, respectively the D 50 -value, can be determined from volume weighted cumulative particle size distributions, wherein the particle size distribution curve can be measured with the help of light scattering methods. [0037]The viscosity of the can inner coating is preferably such that a flow time between 20 and 40 seconds results, when measured with a 4 mm DIN flow cup of DIN EN ISO 2431. If the viscosity, measured as the flow time from the normalized flow cup, is in this range, then the coating, present as a thin film on the inside of the can, has a flow behavior that reduces any run off of the wet film and simultaneously ensures that the can inner coating is able to be applied in spray processes. [0038]Emulsifiers that support the dispersion of the copolymer or the copolymer mixture can be added as an auxiliary to the inventive can inner coating. At least 0.1 wt % of emulsifiers are preferably added for this purpose. Preferably, non-ionic amphiphiles with an HLB value of at least 8 can be additionally comprised as the emulsifiers in the can inner coating. 11 H 09098 PCT [0039]According to the present invention, the HLB value is calculated by the following formula and can assume values of zero to 20 on an arbitrary scale: HLB = 20 (1-Mi/M) with Mi molecular weight of the lipophilic group of the amphiphile M: molecular weight of the amphiphile [0040]The content of this added auxiliary emulsifier in the can inner coating is preferably not more than 5 wt %, particularly preferably not more than 2 wt %. However, the copolymer or the copolymer mixture used in the inventive can inner coating is characterized in that it already possesses self-emulsifying properties as a result of its acid groups. Moreover, it has been shown that the addition of emulsifiers frequently causes a decreased adhesion of the cured can inner coating to the tin plate and aluminum surfaces. Accordingly, in a preferred embodiment of the can inner coating, in the case that the acid number of the copolymer or copolymer mixture is greater than 60 mg KOH / g, preferably greater than 80 mg KOH / g, or the degree of neutralization of the copolymer or copolymer mixture with an acid number below 100 mg KOH / g is at least 30%, then less than 0.1 wt %, particularly preferably less than 0.01 wt % and especially preferably no emulsifiers are comprised that are based on the non-ionic amphiphiles with an HLB value of at least 8. [0041]Alternatively or in addition to the added emulsifiers, the inventive can inner coating may comprise water-miscible organic solvents that decrease the polarity of the aqueous phase, so as to induce the emulsification of the copolymer or copolymer mixture. For this purpose, at least 1 wt % of water miscible organic solvents are added. In this regard, the boiling point of the water-miscible solvent under standard conditions is preferably not more than 150 C. [0042]Suitable solvents are glycol ethers, alcohols and esters. The content of the solvent in the can inner coating is preferably not more than 40 wt %, particularly preferably not more than 20 wt %. 12 H 09098 PCT [0043]Inventive can inner coatings may comprise wetting agents, leveling agents, defoamers, catalysts, film-formers, stabilizers and/or the already mentioned neutralizing agents as additional constituents. These kinds of auxiliaries are generally known to the person skilled in the art of coating objects, wherein film-formers in the present invention are understood to mean organic polymers that can crosslink with the curing agent present in the can inner coating. The content by weight of film-formers based on the copolymer or copolymer mixture is at most 20%, preferably at most 10%. [0044]A preferred formulation of an inventive can inner coating comprises, in addition to at least 40 wt % water, a) 4-30 wt %, preferably 10-20 wt %, of the copolymer or of the copolymer mixture in dispersed form, b) 2-20 wt.%, preferably 4-12 wt.%, of the at least one curing agent, c) not more than 5 wt % of emulsifiers selected from non-ionic amphiphiles with an HLB value of at least 8; d) not more than 40 wt %, preferably at least 1 wt %, of water-miscible organic solvents; e) not more than 10 wt.% of auxiliaries selected from wetting agents, leveling agents, defoamers, catalysts, film-formers, stabilizers and/or neutralizing agents, preferably not more than 12/z pmol of neutralization agent multiplied by the acid number of the copolymer or copolymer mixture are comprised per gram of the copolymer or copolymer mixture where z is the equivalent number of the relevant neutralization reaction. [0045]A particularly preferred reduced-solvent formulation of an inventive can inner coating comprises, in addition to at least 40 wt % water, a) 4-30 wt %, preferably 10-20 wt %, of the copolymer or of the copolymer mixture in dispersed form, 13 H 09098 PCT b) 2-20 wt %, preferably 4-12 wt % of at least one resin, of which at least 40 wt % of a carbodiimide with terminal, blocked isocyanate groups based on the total content of the curing agent, c) not more than 5 wt % of emulsifiers selected from non-ionic amphiphiles with an HLB value of at least 8; d) not more than 10 wt %, preferably not more than 1 wt %, of water miscible organic solvents; e) not more than 10 wt % of auxiliaries selected from wetting agents, leveling agents, defoamers, catalysts, film-formers, stabilizers and/or neutralizing agents, preferably not more than 12/z pmol of neutralization agent multiplied by the acid number of the copolymer or copolymer mixture are comprised per gram of the copolymer or copolymer mixture where z is the equivalent number of the relevant neutralization reaction. [0046] Inventive can inner coatings are characterized in that due to the good crosslinking of the copolymer or of the copolymer mixture with the curing agent, the cured film on the inner surfaces of metal cans possesses excellent barrier properties. The metallic base material is consequently firstly effectively protected against corrosion and secondly the liquid stored in the can will not take up any extraneous substance. Therefore, the present invention makes available an alternative to the conventional use of epoxides in can inner coatings, in particular epoxides based on Bisphenol A. Consequently, the content of epoxidically bonded oxygen in inventive can inner coatings is preferably not more than 0.1 wt %, particularly preferably not more than 0.01 wt %. An inventive can inner coating particularly preferably comprises no organic constituents with epoxide groups. [0047]Inventive can inner coatings can preferably be produced in closed processes in pressure reactors using shear forces, wherein all constituents of an inventive can inner coating are transferred into a pressure reactor, in order to be subsequently subjected to a shear rate of at least 1000 s- at temperatures in the range of 80-200 'C and a pressure of 1-6 bar, wherein the 14 H 09098 PCT energy input is preferably in the range of 10 3 -10 5 J per second per liter of coating formulation. Alternatively, the solid constituents together with the usual components of the can inner coating are also dispersed in an open process, in which the melted copolymer or the melted copolymer mixture under the action of the abovementioned shear force is transferred into the aqueous composition of the usual can inner coating composition. However, the shear rate and residence time in each dispersion process is preferably adjusted such that the dispersed constituents of the can inner coating have a Doo value of not more than 100 pm, wherein the D 50 value is preferably not below 1 pm, particularly preferably not below 10 pm. [0048]The application of a wet film of the inventive can inner coating is preferably carried out in a spray process, particularly preferably in the "Airless Process", in which the can inner coating is airlessly atomized and thus deposited onto the material surface. In this spray process, a defined quantity of the can inner coating is introduced into the cleaned and dried can interior by means of spray guns, while the can is rotated about its own longitudinal axis in order to form a homogeneous film. The wet film on the can inner surface is then cured to a coating film in a drying oven at temperatures ranging between 120 0 C and 200 *C (object temperature). The curing process includes the volatilization of the aqueous phase as well as the film formation and crosslinking of the polymeric constituents. [0049]In another aspect, the present invention relates to the use of a copolymer or a copolymer mixture of at least one aliphatic and acyclic alkene with at least one a,p-unsaturated carboxylic acid in water-dispersed form, wherein the acid number of the copolymer or of the copolymer mixture is at least 20 mg KOH / g, but not more than 200 mg KOH / g, and the acid groups of the copolymer or of the copolymer mixture in the water-dispersed form are at least 20%, but not more than 70% neutralized, as a constituent of water-based can inner coatings, wherein preferred uses can be realized by above described corresponding embodiments of the copolymer or of the copolymer mixture. 15 H 09098 PCT [0050] In another aspect, the present invention relates to the use of an above described can inner coating that is deposited in a dry film thickness of at least 5 g/m 2 , but preferably of not more than 50 g/m 2 , on to the inner surface of a tin plate can and in a dry film thickness of at least 1.5 g/m 2 , but preferably not more than 50 g/m 2 , on to the inner surface of an aluminum can. 16 H 09098 PCT Examples: Table 1 lists the compositions of the inventive can inner coatings that were deposited as a wet film on to the inner surfaces of tin plate cans by means of spray processes, and then cured for 40 seconds at 180 0 C to a dry coating with a coating weight of 6-7 g/m 2 . The water-based can inner coatings were manufactured in an open reactor by continuously metering the melted copolymer to an aqueous composition of the remaining constituents under a shear stress of 1500 s- at 95 0 C. After metering in the copolymer, the homogenization was continued in the open reactor until a constant viscosity of the coating formulation was achieved. The viscosity of the coating formulations, measured as the flow time from a DIN 4 mm flow cup according to DIN EN ISO 2431 lay in the range 25-28 seconds. The coating formulations homogenized in this way were then deposited onto the inner surfaces of the tin plate can in a two-step spray process, wherein the tin plate can was rotated about an axis and initially the bottom of the can and lower part of the body was coated and then the can body and end were sprayed. The wet film was then cured. From Table 2 it can be seen that the tin plate cans coated with the inventive coating possess an excellent flexibility (T-bend test) and water resistance (Koch test). Solely the hardness and solvent resistance tests showed differing results, which, however, all met the requirements of the beverage can industry. 17 cfco U)? C ) 0 0 LO L - CN c 0 U) U) ii No N N D Ua) a) CD 0 Ua)
OE
C) 00 0 1--U C-4, U ~ U U) t )U UY) UY) ) a 0s 00 0U) c U) ) a nC 0 CC o 0 > ~ cu CUa D : 4- ~~~- a 'U G 0u E U) U) 0 0 o: 0 0 a C C E. E > 0 0 M Q.~ C%4 oz iE., a) Cu Cu = - a I. Cu C) U) L C0- Cu Lo C"u 0)l C 4-C. C V U C a) CD(D C _D C cm ~0 a C. a) a)) U - E cc 0 0 C3 0 o0 0. 0 */ in 50 ~ U (3) c~r) C) co 0 om mNC) 0 c0 C co 0c ml 00 CL C) Ul) 0~0 LOCU C V 4-* LO O .0 E *-f) L Cu LO Wu '- _ '- Cf L( z U' U) 0No L 0 : Z M - cn Lc) Cu Li - 0 Cc Ur 0-""0 U)) C) Z 50 4-- . c 5 0. L) EO vl Cu Cu C a) C: U ) H MC '1 C.W .4-i C) , ~ . 0) Co CO C '4- 'a.() 0 0) 04 C) C) ) a) c cr 0H C) Lp v a) 0 0 a 0 0 0 C) N n
Claims (15)
1. A water-based can inner coating comprising, in addition to water, a) a copolymer or a copolymer mixture of at least one aliphatic and acyclic alkene with at least one a,p-unsaturated carboxylic acid and at least one ester of a,@-unsaturated carboxylic acids in water dispersed form, wherein the acid number of the copolymer or of the copolymer mixture is at least 20 mg KOH/g, but less than 100 mg KOH/g, and b) at least one water-dispersed or water-soluble curing agent selected from the group of aminoplasts and/or the group of carbodiimides.
2. The can inner coating according to claim 1, wherein the acid groups of the copolymer or of the copolymer mixture in the water-dispersed form are at least partially, preferably to at least 20%, particularly preferably to at least 30%, but preferably not more than 70%, particularly preferably not more than 60% neutralized.
3. The can inner coating according to claim 2, comprising ammonia, amines, metallic Al or Zn and/or water-soluble oxides and hydroxides of the elements Li, Na, K, Mg, Ca, Fe(Il), Sn(ll) as the neutralization agent for neutralizing the acid groups of the copolymer or of the copolymer mixture in water-dispersed form.
4. The can inner coating according to claim 3, wherein the neutralization agent is selected from ammonia and/or amines, wherein the amines are again preferably selected from morpholine, hydrazine, hydroxylamine, monoethanolamine, diethanolamine, triethanolamine, dimethylethanolamine and/or diethylethanolamine.
5. The can inner coating according to any one of the previous claims, wherein the copolymer or the copolymer mixture has a glass transition temperature of not more than 80 "C, preferably not more than 60 *C. 21
6. The can inner coating according to any one of the previous claims, wherein the aliphatic and acyclic alkene is selected from ethene, propane, 1-butene, 2-butene, isobutene, 1,3-butadiene and/or 2 methylbuta-1,3-diene, preferably ethene.
7. The can inner coating according to any one of the previous claims, wherein the a,p-unsaturated carboxylic acids are selected from cinnamic acid, crotonic acid, fumaric acid, itaconic acid, maleic acid, acrylic acid and/or methacrylic acid, preferably acrylic acid and/or methacrylic acid, particularly preferably acrylic acid.
8. The can inner coating according to any one of the previous claims, wherein the weight fraction of the aliphatic and acyclic alkenes in the copolymer or in the copolymer mixture is at least 40 wt.%, preferably at least 60 wt.%, but not more than 95 wt.%.
9. The can inner coating according to any one of the previous claims, wherein the comonomers selected from esters of a,o-unsaturated carboxylic acids are linear or branched alkyl esters of the acrylic acid and/or methacrylic acid containing not more than 12 carbon atoms in the aliphatic group wherein the copolymer or the copolymer mixture preferably has an acid number of less than 60 mg KOH/g.
10. The can inner coating according to any one of the previous claims, wherein the dispersed polymeric constituents of the water based coating have a Dqo value of not more than 100 pm, preferably not more than 60 pm and a D 50 value of not less than 1 pm, preferably not less than 10 pm.
11. The can inner coating according to any one of the previous claims, comprising at least 40 wt.% water and a) 4-30 wt.% preferably 10-20 wt.%, of the copolymer or of the copolymer mixture in dispersed form, b) 2-20 wt.%, preferably 4-12 wt.% of the at least one curing agent, c) not more than 5 wt.% of emulsifiers selected from non-ionic amphiphiles with an HLB value of at least 8; 22 d) not more than 40 wt.%, preferably at least 5 wt.%, of water-miscible organic solvents; e) not more than 10 wt.% of auxiliaries selected from wetting agents, leveling agents, defoamers, catalysts, film-formers, stabilizers and/or neutralizing agents.
12. Use of a copolymer or a copolymer mixture of at least one aliphatic and acyclic alkene with at least one a,-unsaturated carboxylic acid and at least one ester of a,p-unsaturated carboxylic acids in water dispersed form, wherein the acid number of the copolymer or of the copolymer mixture is at least 20 mg KOH/g, but less than 100 mg KOH/g, and the acid groups of the copolymer or of the copolymer mixture in the water-dispersed form are at least 20%, but not more than 70% neutralized, as a constituent of the water-based can inner coating.
13. Use of a can inner coating according to any one of claims 1 to 11, wherein the inner coating is deposited in a dry film thickness of at least 5 g/m 2 , but preferably in a dry film thickness of not more than 50 g/m 2 , on to the inner surface of a tin plate can.
14. Use of a can inner coating according to any one of claims I to 11, wherein the inner coating is deposited in a dry film thickness of at least 1.5 g/m 2 , but preferably in a dry film thickness of not more than 50 g/m 2 , on to the inner surface of an aluminum can.
15. The use according to claim 13 or 14, wherein the can inner coating is deposited in the spray process. Henkel AG & Co. KGaA Patent Attorneys for the Applicant/Nominated Person SPRUSON & FERGUSON
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP11160695.0 | 2011-03-31 | ||
| EP11160695A EP2505625B1 (en) | 2011-03-31 | 2011-03-31 | Varnishing formula for the interior surface of cans |
| PCT/EP2012/053830 WO2012130563A1 (en) | 2011-03-31 | 2012-03-07 | Coating formulation for the interior surfaces of cans |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| AU2012237371A1 AU2012237371A1 (en) | 2013-10-17 |
| AU2012237371B2 true AU2012237371B2 (en) | 2015-09-17 |
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AU2012237371A Ceased AU2012237371B2 (en) | 2011-03-31 | 2012-03-07 | Coating formulation for the interior surfaces of cans |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US20140023782A1 (en) |
| EP (2) | EP2505625B1 (en) |
| JP (1) | JP2014514392A (en) |
| CN (1) | CN103619974A (en) |
| AU (1) | AU2012237371B2 (en) |
| CA (1) | CA2831808A1 (en) |
| ES (1) | ES2416466T3 (en) |
| PL (1) | PL2505625T3 (en) |
| WO (1) | WO2012130563A1 (en) |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE102012223355A1 (en) * | 2012-12-17 | 2014-06-18 | Henkel Ag & Co. Kgaa | Highly crosslinking paint formulation for inside can surfaces |
| DE102012223356A1 (en) | 2012-12-17 | 2014-06-18 | Henkel Ag & Co. Kgaa | Process for producing coated can ends |
| DE102015208076A1 (en) * | 2015-04-30 | 2016-11-03 | Henkel Ag & Co. Kgaa | Method for sealing oxidic protective layers on metal substrates |
| EP3402850A1 (en) * | 2016-01-15 | 2018-11-21 | PPG Industries Ohio, Inc. | A coating composition comprising a thermoset resin and a thermoplastic resin |
| US20170204289A1 (en) | 2016-01-15 | 2017-07-20 | Ppg Industries Ohio, Inc. | Hydroxy functional alkyl polyurea |
| US10808144B2 (en) * | 2017-05-22 | 2020-10-20 | Ppg Industries Ohio, Inc. | Polyolefin silicon coating composition |
| CN115812090B (en) * | 2020-06-12 | 2024-11-26 | Swimc有限公司 | Coating compositions for beverage containers |
| CN115867620B (en) * | 2020-06-12 | 2025-03-28 | Swimc有限公司 | Coating compositions for beverage containers |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2005075878A (en) * | 2003-08-29 | 2005-03-24 | Mitsui Chemicals Inc | Composition for water dispersion type rust-preventing coating |
Family Cites Families (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS4923227A (en) * | 1972-05-08 | 1974-03-01 | ||
| US3908049A (en) * | 1972-06-05 | 1975-09-23 | Continental Can Co | Method for coating metal surfaces with aqueous dispersions of carboxyl containing polymers |
| US3991216A (en) * | 1974-05-16 | 1976-11-09 | Ppg Industries, Inc. | Beverage containers coated with a water based liner |
| CA1054870A (en) * | 1974-05-20 | 1979-05-22 | Ihab M. Hekal | Method for coating metal container body interiors with aqueous dispersed resin coating materials |
| JPS58168665A (en) * | 1982-03-30 | 1983-10-05 | Kansai Paint Co Ltd | Water base paint for inner surface of food can |
| US4948834A (en) * | 1989-03-27 | 1990-08-14 | Ppg Industries, Inc. | Vinyl chloride-olefin copolymers having good color stability and flexibility for container coatings |
| JP4652592B2 (en) * | 2001-03-15 | 2011-03-16 | 日本ペイント株式会社 | Metal surface treatment agent |
| US20030059618A1 (en) | 2001-03-23 | 2003-03-27 | Hideyuke Takai | Method of producing epoxy compound, epoxy resin composition and its applications, ultraviolet rays-curable can-coating composition and method of producing coated metal can |
| EP1584638A1 (en) | 2004-03-29 | 2005-10-12 | Imperial Chemical Industries Plc. | Coating composition based on modified epoxy resins |
| EP2420542B2 (en) | 2004-10-20 | 2018-09-19 | Valspar Sourcing, Inc. | Article and method of coating |
| KR101719843B1 (en) * | 2009-07-24 | 2017-03-24 | 다우 글로벌 테크놀로지스 엘엘씨 | Coated container device, method of making the same |
-
2011
- 2011-03-31 ES ES11160695T patent/ES2416466T3/en active Active
- 2011-03-31 PL PL11160695T patent/PL2505625T3/en unknown
- 2011-03-31 EP EP11160695A patent/EP2505625B1/en not_active Revoked
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2012
- 2012-03-07 EP EP12707311.2A patent/EP2691483A1/en not_active Withdrawn
- 2012-03-07 AU AU2012237371A patent/AU2012237371B2/en not_active Ceased
- 2012-03-07 CA CA2831808A patent/CA2831808A1/en not_active Abandoned
- 2012-03-07 WO PCT/EP2012/053830 patent/WO2012130563A1/en not_active Ceased
- 2012-03-07 JP JP2014501512A patent/JP2014514392A/en active Pending
- 2012-03-07 CN CN201280016344.0A patent/CN103619974A/en active Pending
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2013
- 2013-09-24 US US14/034,753 patent/US20140023782A1/en not_active Abandoned
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2005075878A (en) * | 2003-08-29 | 2005-03-24 | Mitsui Chemicals Inc | Composition for water dispersion type rust-preventing coating |
Also Published As
| Publication number | Publication date |
|---|---|
| WO2012130563A1 (en) | 2012-10-04 |
| AU2012237371A1 (en) | 2013-10-17 |
| CN103619974A (en) | 2014-03-05 |
| US20140023782A1 (en) | 2014-01-23 |
| EP2505625A1 (en) | 2012-10-03 |
| EP2505625B1 (en) | 2013-03-27 |
| ES2416466T3 (en) | 2013-08-01 |
| PL2505625T3 (en) | 2013-11-29 |
| JP2014514392A (en) | 2014-06-19 |
| CA2831808A1 (en) | 2012-10-04 |
| EP2691483A1 (en) | 2014-02-05 |
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