CA1065524A - Garnitures a base aqueuse pour recipients de boissons - Google Patents

Garnitures a base aqueuse pour recipients de boissons

Info

Publication number: CA1065524A
Authority: CA; Canada
Prior art keywords: percent; water; interpolymer; tlle; weight
Prior art date: 1974-05-16
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

Application number

CA318,452A

Other languages

English (en)

Inventor

Roger M. Christenson

Rudolf Maska

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

PPG Industries Inc

Original Assignee

PPG Industries Inc

Priority date (The priority date 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 date listed.)

1974-05-16

Filing date

1978-12-21

Publication date

1979-10-30

1974-08-05 Priority claimed from US05/494,688 external-priority patent/US4097438A/en

1975-04-04 Priority claimed from CA223,852A external-priority patent/CA1065988A/fr

1978-12-21 Application filed by PPG Industries Inc filed Critical PPG Industries Inc

1978-12-21 Priority to CA318,452A priority Critical patent/CA1065524A/fr

1979-10-30 Application granted granted Critical

1979-10-30 Publication of CA1065524A publication Critical patent/CA1065524A/fr

Status Expired legal-status Critical Current

Links

XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 title claims abstract description 59
235000013361 beverage Nutrition 0.000 title claims abstract description 24
239000000203 mixture Substances 0.000 claims abstract description 81
239000000178 monomer Substances 0.000 claims abstract description 28
150000001412 amines Chemical class 0.000 claims abstract description 25
239000007787 solid Substances 0.000 claims abstract description 25
239000002253 acid Substances 0.000 claims abstract description 24
239000008199 coating composition Substances 0.000 claims abstract description 21
229920005989 resin Polymers 0.000 claims abstract description 21
239000011347 resin Substances 0.000 claims abstract description 21
150000003839 salts Chemical class 0.000 claims abstract description 20
HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 claims abstract description 17
239000003960 organic solvent Substances 0.000 claims abstract description 16
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims abstract description 14
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims abstract description 13
229910052751 metal Inorganic materials 0.000 claims abstract description 13
239000002184 metal Substances 0.000 claims abstract description 13
229920002554 vinyl polymer Polymers 0.000 claims abstract description 13
239000007788 liquid Substances 0.000 claims abstract description 12
SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims abstract description 11
NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims abstract description 11
FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical compound CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 claims abstract description 10
LSDPWZHWYPCBBB-UHFFFAOYSA-N Methanethiol Chemical compound SC LSDPWZHWYPCBBB-UHFFFAOYSA-N 0.000 claims abstract description 9
229910052739 hydrogen Chemical group 0.000 claims abstract description 9
239000001257 hydrogen Chemical group 0.000 claims abstract description 9
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims abstract description 9
JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 claims abstract description 7
PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 claims abstract description 7
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical group [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract description 5
238000012856 packing Methods 0.000 claims abstract description 5
239000002685 polymerization catalyst Substances 0.000 claims abstract description 5
125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract description 4
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims abstract description 4
239000007921 spray Substances 0.000 claims abstract description 3
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 claims description 35
LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 claims description 12
POAOYUHQDCAZBD-UHFFFAOYSA-N 2-butoxyethanol Chemical compound CCCCOCCO POAOYUHQDCAZBD-UHFFFAOYSA-N 0.000 claims description 7
ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 claims description 5
230000003472 neutralizing effect Effects 0.000 claims description 4
HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 claims description 2
UEEJHVSXFDXPFK-UHFFFAOYSA-N N-dimethylaminoethanol Chemical group CN(C)CCO UEEJHVSXFDXPFK-UHFFFAOYSA-N 0.000 claims description 2
229960002887 deanol Drugs 0.000 claims description 2
239000012972 dimethylethanolamine Substances 0.000 claims description 2
150000001408 amides Chemical class 0.000 description 19
229960004592 isopropanol Drugs 0.000 description 16
238000000576 coating method Methods 0.000 description 15
229940117913 acrylamide Drugs 0.000 description 14
239000002904 solvent Substances 0.000 description 14
238000006386 neutralization reaction Methods 0.000 description 13
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 12
238000000034 method Methods 0.000 description 12
239000000243 solution Substances 0.000 description 12
235000013405 beer Nutrition 0.000 description 11
239000011248 coating agent Substances 0.000 description 11
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 9
125000000217 alkyl group Chemical group 0.000 description 8
125000004432 carbon atom Chemical group C* 0.000 description 7
238000012360 testing method Methods 0.000 description 7
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 6
239000003054 catalyst Substances 0.000 description 6
239000003795 chemical substances by application Substances 0.000 description 6
239000000463 material Substances 0.000 description 6
238000006116 polymerization reaction Methods 0.000 description 6
238000003860 storage Methods 0.000 description 6
239000006185 dispersion Substances 0.000 description 5
239000000758 substrate Substances 0.000 description 5
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
-1 alkyl methacrylates Chemical class 0.000 description 4
238000002360 preparation method Methods 0.000 description 4
239000011877 solvent mixture Substances 0.000 description 4
238000012546 transfer Methods 0.000 description 4
230000002411 adverse Effects 0.000 description 3
230000032683 aging Effects 0.000 description 3
238000013019 agitation Methods 0.000 description 3
238000007598 dipping method Methods 0.000 description 3
150000002148 esters Chemical class 0.000 description 3
229960004279 formaldehyde Drugs 0.000 description 3
235000019256 formaldehyde Nutrition 0.000 description 3
150000002500 ions Chemical class 0.000 description 3
229910052757 nitrogen Inorganic materials 0.000 description 3
238000009928 pasteurization Methods 0.000 description 3
229920000642 polymer Polymers 0.000 description 3
238000000926 separation method Methods 0.000 description 3
238000005507 spraying Methods 0.000 description 3
HGINCPLSRVDWNT-UHFFFAOYSA-N Acrolein Chemical compound C=CC=O HGINCPLSRVDWNT-UHFFFAOYSA-N 0.000 description 2
NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 2
101150014183 Alpl gene Proteins 0.000 description 2
239000004215 Carbon black (E152) Substances 0.000 description 2
102100024133 Coiled-coil domain-containing protein 50 Human genes 0.000 description 2
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 description 2
101000910772 Homo sapiens Coiled-coil domain-containing protein 50 Proteins 0.000 description 2
CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 2
YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 description 2
101100238304 Mus musculus Morc1 gene Proteins 0.000 description 2
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
239000000654 additive Substances 0.000 description 2
150000001298 alcohols Chemical class 0.000 description 2
229910052782 aluminium Inorganic materials 0.000 description 2
XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
230000015572 biosynthetic process Effects 0.000 description 2
238000009835 boiling Methods 0.000 description 2
230000001680 brushing effect Effects 0.000 description 2
239000012986 chain transfer agent Substances 0.000 description 2
238000006243 chemical reaction Methods 0.000 description 2
LDHQCZJRKDOVOX-NSCUHMNNSA-N crotonic acid Chemical compound C\C=C\C(O)=O LDHQCZJRKDOVOX-NSCUHMNNSA-N 0.000 description 2
RWGFKTVRMDUZSP-UHFFFAOYSA-N cumene Chemical compound CC(C)C1=CC=CC=C1 RWGFKTVRMDUZSP-UHFFFAOYSA-N 0.000 description 2
239000008367 deionised water Substances 0.000 description 2
238000004821 distillation Methods 0.000 description 2
235000011087 fumaric acid Nutrition 0.000 description 2
150000002238 fumaric acids Chemical class 0.000 description 2
238000010438 heat treatment Methods 0.000 description 2
229930195733 hydrocarbon Natural products 0.000 description 2
150000002430 hydrocarbons Chemical class 0.000 description 2
150000002689 maleic acids Chemical class 0.000 description 2
239000003791 organic solvent mixture Substances 0.000 description 2
230000000379 polymerizing effect Effects 0.000 description 2
HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical compound C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 description 2
230000007928 solubilization Effects 0.000 description 2
238000005063 solubilization Methods 0.000 description 2
238000003756 stirring Methods 0.000 description 2
GJBRNHKUVLOCEB-UHFFFAOYSA-N tert-butyl benzenecarboperoxoate Chemical compound CC(C)(C)OOC(=O)C1=CC=CC=C1 GJBRNHKUVLOCEB-UHFFFAOYSA-N 0.000 description 2
LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 description 2
239000008096 xylene Substances 0.000 description 2
XLYMOEINVGRTEX-ONEGZZNKSA-N (e)-4-ethoxy-4-oxobut-2-enoic acid Chemical compound CCOC(=O)\C=C\C(O)=O XLYMOEINVGRTEX-ONEGZZNKSA-N 0.000 description 1
GHKCSRZBNZQHKW-UHFFFAOYSA-N 1-sulfanylethanol Chemical group CC(O)S GHKCSRZBNZQHKW-UHFFFAOYSA-N 0.000 description 1
JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 description 1
FWWOWPGPERBCNJ-UHFFFAOYSA-N 2-hydroxy-4-(2-hydroxyethoxy)-4-oxobutanoic acid Chemical compound OCCOC(=O)CC(O)C(O)=O FWWOWPGPERBCNJ-UHFFFAOYSA-N 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
VVNCNSJFMMFHPL-VKHMYHEASA-N D-penicillamine Chemical compound CC(C)(S)[C@@H](N)C(O)=O VVNCNSJFMMFHPL-VKHMYHEASA-N 0.000 description 1
101100353161 Drosophila melanogaster prel gene Proteins 0.000 description 1
229920006063 Lamide® Polymers 0.000 description 1
241000234435 Lilium Species 0.000 description 1
CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 1
YFONKFDEZLYQDH-OPQQBVKSSA-N N-[(1R,2S)-2,6-dimethyindan-1-yl]-6-[(1R)-1-fluoroethyl]-1,3,5-triazine-2,4-diamine Chemical compound C[C@@H](F)C1=NC(N)=NC(N[C@H]2C3=CC(C)=CC=C3C[C@@H]2C)=N1 YFONKFDEZLYQDH-OPQQBVKSSA-N 0.000 description 1
OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
241000428533 Rhis Species 0.000 description 1
229910000831 Steel Inorganic materials 0.000 description 1
ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical group OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
230000002378 acidificating effect Effects 0.000 description 1
150000003926 acrylamides Chemical class 0.000 description 1
150000001252 acrylic acid derivatives Chemical class 0.000 description 1
230000001464 adherent effect Effects 0.000 description 1
238000003915 air pollution Methods 0.000 description 1
125000003545 alkoxy group Chemical group 0.000 description 1
125000004849 alkoxymethyl group Chemical group 0.000 description 1
125000004106 butoxy group Chemical group [*]OC([H])([H])C([H])([H])C(C([H])([H])[H])([H])[H] 0.000 description 1
CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 1
235000012174 carbonated soft drink Nutrition 0.000 description 1
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
239000010960 cold rolled steel Substances 0.000 description 1
229940000425 combination drug Drugs 0.000 description 1
150000001875 compounds Chemical class 0.000 description 1
238000011109 contamination Methods 0.000 description 1
238000005336 cracking Methods 0.000 description 1
239000003431 cross linking reagent Substances 0.000 description 1
229910021641 deionized water Inorganic materials 0.000 description 1
229940075911 depen Drugs 0.000 description 1
ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 1
229940043237 diethanolamine Drugs 0.000 description 1
239000012153 distilled water Substances 0.000 description 1
GMSCBRSQMRDRCD-UHFFFAOYSA-N dodecyl 2-methylprop-2-enoate Chemical compound CCCCCCCCCCCCOC(=O)C(C)=C GMSCBRSQMRDRCD-UHFFFAOYSA-N 0.000 description 1
239000000839 emulsion Substances 0.000 description 1
238000003912 environmental pollution Methods 0.000 description 1
238000006266 etherification reaction Methods 0.000 description 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
238000009472 formulation Methods 0.000 description 1
235000015203 fruit juice Nutrition 0.000 description 1
XLYMOEINVGRTEX-UHFFFAOYSA-N fumaric acid monoethyl ester Natural products CCOC(=O)C=CC(O)=O XLYMOEINVGRTEX-UHFFFAOYSA-N 0.000 description 1
238000011065 in-situ storage Methods 0.000 description 1
239000003112 inhibitor Substances 0.000 description 1
239000000976 ink Substances 0.000 description 1
LRDFRRGEGBBSRN-UHFFFAOYSA-N isobutyronitrile Chemical compound CC(C)C#N LRDFRRGEGBBSRN-UHFFFAOYSA-N 0.000 description 1
238000004811 liquid chromatography Methods 0.000 description 1
229940102689 lustra Drugs 0.000 description 1
VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
239000011976 maleic acid Substances 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
150000002739 metals Chemical class 0.000 description 1
125000005395 methacrylic acid group Chemical group 0.000 description 1
XMYQHJDBLRZMLW-UHFFFAOYSA-N methanolamine Chemical compound NCO XMYQHJDBLRZMLW-UHFFFAOYSA-N 0.000 description 1
LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 1
VIKNJXKGJWUCNN-XGXHKTLJSA-N norethisterone Chemical compound O=C1CC[C@@H]2[C@H]3CC[C@](C)([C@](CC4)(O)C#C)[C@@H]4[C@@H]3CCC2=C1 VIKNJXKGJWUCNN-XGXHKTLJSA-N 0.000 description 1
230000000063 preceeding effect Effects 0.000 description 1
238000012545 processing Methods 0.000 description 1
BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
238000003908 quality control method Methods 0.000 description 1
239000000376 reactant Substances 0.000 description 1
239000011541 reaction mixture Substances 0.000 description 1
238000010992 reflux Methods 0.000 description 1
239000011342 resin composition Substances 0.000 description 1
MWNQXXOSWHCCOZ-UHFFFAOYSA-L sodium;oxido carbonate Chemical compound [Na+].[O-]OC([O-])=O MWNQXXOSWHCCOZ-UHFFFAOYSA-L 0.000 description 1
230000003381 solubilizing effect Effects 0.000 description 1
239000003381 stabilizer Substances 0.000 description 1
239000010959 steel Substances 0.000 description 1
125000001424 substituent group Chemical group 0.000 description 1
125000000547 substituted alkyl group Chemical group 0.000 description 1
239000004094 surface-active agent Substances 0.000 description 1
239000008399 tap water Substances 0.000 description 1
235000020679 tap water Nutrition 0.000 description 1
230000009967 tasteless effect Effects 0.000 description 1
229920001897 terpolymer Polymers 0.000 description 1
125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
229920001187 thermosetting polymer Polymers 0.000 description 1
239000005029 tin-free steel Substances 0.000 description 1
239000005028 tinplate Substances 0.000 description 1
VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
239000011850 water-based material Substances 0.000 description 1

Landscapes

Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Paints Or Removers (AREA)

CA318,452A 1974-05-16 1978-12-21 Garnitures a base aqueuse pour recipients de boissons Expired CA1065524A (fr)

Priority Applications (1)

Application Number	Priority Date	Filing Date	Title
CA318,452A CA1065524A (fr)	1974-05-16	1978-12-21	Garnitures a base aqueuse pour recipients de boissons

Applications Claiming Priority (4)

Application Number	Priority Date	Filing Date	Title
US47048074A	1974-05-16	1974-05-16
US05/494,688 US4097438A (en)	1974-05-16	1974-08-05	Water-based liners for beverage containers
CA223,852A CA1065988A (fr)	1974-05-16	1975-04-04	Garnitures aquiferes pour cannettes
CA318,452A CA1065524A (fr)	1974-05-16	1978-12-21	Garnitures a base aqueuse pour recipients de boissons

Publications (1)

Publication Number	Publication Date
CA1065524A true CA1065524A (fr)	1979-10-30

Family

ID=27425836

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CA318,452A Expired CA1065524A (fr)	1974-05-16	1978-12-21	Garnitures a base aqueuse pour recipients de boissons

Country Status (1)

Country	Link
CA (1)	CA1065524A (fr)

1978
- 1978-12-21 CA CA318,452A patent/CA1065524A/fr not_active Expired

Publication	Publication Date	Title
US3991216A (en)	1976-11-09	Beverage containers coated with a water based liner
CA1145080A (fr)	1983-04-19	Compositions de revetement aqueuses, renfermant des oligomeres acryliques, polymeres de poids moleculaire eleve et des reticulants
US4341679A (en)	1982-07-27	Vinylidene chloride co-polymer latex compositions
US4170582A (en)	1979-10-09	Process for preparing a polymer resin aqueous dispersion
US4304703A (en)	1981-12-08	Cationic polymer dispersions and their method of preparation
US5070136A (en)	1991-12-03	Aqueous polymer dispersions for coating wood
US7475786B2 (en)	2009-01-13	Can coatings, methods for coating can and cans coated thereby
CA1131824A (fr)	1982-09-14	Revetements en copolymere acrylique
US5912293A (en)	1999-06-15	Aqueous polymer dispersions for coating wood
CA2095117A1 (fr)	1992-04-30	Compositions pour le revetement de contenant metallique
CA1065988A (fr)	1979-11-06	Garnitures aquiferes pour cannettes
US4097438A (en)	1978-06-27	Water-based liners for beverage containers
EP0030080B2 (fr)	1990-04-11	Compositions de latex de copolymères de chlorure de vinylidène et procédé de revêtement avec celles-ci
EP0171235B1 (fr)	1992-04-15	Compositions de revêtement, en particulier pour substrats de bois à base de dispersions non aqueuses de copolymères d'éthylacrylate qui ont une extensibilité et une quantité de gel bien définies
US5030684A (en)	1991-07-09	Acrylate copolymers containing hydroxyl and fluorine groups as additives for aqueous anionic paint systems
US4477609A (en)	1984-10-16	Hydrosol coating compositions having improved stability
AU2018248576B2 (en)	2023-11-23	Coating compositions containing a hydroxyphenyl functional polymer and a latex polymer
CA1248671A (fr)	1989-01-10	ENDUITS A TENEUR DE TERPOLYMERE D'OLEFINE .alpha.
CA1065524A (fr)	1979-10-30	Garnitures a base aqueuse pour recipients de boissons
US5270414A (en)	1993-12-14	Copolymer coating
CA2132275A1 (fr)	1995-04-07	Aminosilanes pour correcteur liquide aqueux ne produisant pas de bavures
US3347700A (en)	1967-10-17	Coated containers
CA1071342A (fr)	1980-02-05	Compositions de revetement de liaison en suspension aqueuse pour couches de fond et d'appret a utiliser sur des contenants a boisson en acier non etame en trois elements
AU695707B2 (en)	1998-08-20	Aqueous polymer dispersions for coating wood
US4845147A (en)	1989-07-04	Nonaqueous polymer dispersions