DE19703091A1 - Überzugsmittel für Nahrungsmittelbehälter - Google Patents

Überzugsmittel für Nahrungsmittelbehälter

Info

Publication number: DE19703091A1
Authority: DE; Germany
Prior art keywords: weight; water; coating; coating agent; koh
Prior art date: 1997-01-29
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

Application number

DE19703091A

Other languages

German (de)

English (en)

Inventor

Gerrit Jungheim

Juergen Erwin Lemke

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 Ohio 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.)

1997-01-29

Filing date

1997-01-29

Publication date

1998-07-30

1997-01-29 Application filed by PPG Industries Inc filed Critical PPG Industries Inc

1997-01-29 Priority to DE19703091A priority Critical patent/DE19703091A1/de

1997-12-10 Priority to AU57560/98A priority patent/AU5756098A/en

1997-12-10 Priority to KR1019997006854A priority patent/KR20000070606A/ko

1997-12-10 Priority to PCT/EP1997/006906 priority patent/WO1998032807A1/fr

1997-12-10 Priority to EP97953778A priority patent/EP0956321A1/fr

1997-12-10 Priority to BR9714327-8A priority patent/BR9714327A/pt

1997-12-10 Priority to CA002278351A priority patent/CA2278351A1/fr

1998-07-30 Publication of DE19703091A1 publication Critical patent/DE19703091A1/de

Status Ceased legal-status Critical Current

Links

235000013305 food Nutrition 0.000 title claims abstract description 18
239000011248 coating agent Substances 0.000 title claims description 72
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 31
229920002803 thermoplastic polyurethane Polymers 0.000 claims abstract description 25
229920001225 polyester resin Polymers 0.000 claims abstract description 23
239000004645 polyester resin Substances 0.000 claims abstract description 23
239000011230 binding agent Substances 0.000 claims abstract description 22
229920000642 polymer Polymers 0.000 claims abstract description 21
229920000058 polyacrylate Polymers 0.000 claims abstract description 15
238000004132 cross linking Methods 0.000 claims abstract description 11
239000003960 organic solvent Substances 0.000 claims abstract description 9
239000008199 coating composition Substances 0.000 claims abstract 4
238000000576 coating method Methods 0.000 claims description 32
POAOYUHQDCAZBD-UHFFFAOYSA-N 2-butoxyethanol Chemical compound CCCCOCCO POAOYUHQDCAZBD-UHFFFAOYSA-N 0.000 claims description 22
LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 claims description 19
239000002904 solvent Substances 0.000 claims description 18
239000000203 mixture Substances 0.000 claims description 17
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 12
NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 11
238000004519 manufacturing process Methods 0.000 claims description 8
CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims description 5
JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 claims description 4
229920000877 Melamine resin Polymers 0.000 claims description 4
238000006386 neutralization reaction Methods 0.000 claims description 4
PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 claims description 4
239000000049 pigment Substances 0.000 claims description 4
229920006395 saturated elastomer Polymers 0.000 claims description 4
239000004640 Melamine resin Substances 0.000 claims description 3
239000000314 lubricant Substances 0.000 claims description 3
238000006116 polymerization reaction Methods 0.000 claims description 3
238000007334 copolymerization reaction Methods 0.000 claims description 2
150000007974 melamines Chemical class 0.000 claims description 2
239000007858 starting material Substances 0.000 claims description 2
ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 claims 1
125000002252 acyl group Chemical group 0.000 claims 1
239000005056 polyisocyanate Substances 0.000 description 18
229920001228 polyisocyanate Polymers 0.000 description 18
229920005989 resin Polymers 0.000 description 16
239000011347 resin Substances 0.000 description 16
238000004659 sterilization and disinfection Methods 0.000 description 16
238000000034 method Methods 0.000 description 15
230000001954 sterilising effect Effects 0.000 description 14
125000002887 hydroxy group Chemical group [H]O* 0.000 description 12
ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 9
238000005516 engineering process Methods 0.000 description 7
229920000728 polyester Polymers 0.000 description 7
239000000047 product Substances 0.000 description 7
OAYXUHPQHDHDDZ-UHFFFAOYSA-N 2-(2-butoxyethoxy)ethanol Chemical compound CCCCOCCOCCO OAYXUHPQHDHDDZ-UHFFFAOYSA-N 0.000 description 6
SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 6
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
UEEJHVSXFDXPFK-UHFFFAOYSA-N N-dimethylaminoethanol Chemical compound CN(C)CCO UEEJHVSXFDXPFK-UHFFFAOYSA-N 0.000 description 6
229960002887 deanol Drugs 0.000 description 6
239000012972 dimethylethanolamine Substances 0.000 description 6
238000009928 pasteurization Methods 0.000 description 6
-1 aliphatic dicarboxylic acids Chemical class 0.000 description 5
229920003180 amino resin Polymers 0.000 description 5
239000000126 substance Substances 0.000 description 5
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 4
239000000654 additive Substances 0.000 description 4
150000001298 alcohols Chemical class 0.000 description 4
125000001931 aliphatic group Chemical group 0.000 description 4
230000007613 environmental effect Effects 0.000 description 4
239000003822 epoxy resin Substances 0.000 description 4
150000002148 esters Chemical class 0.000 description 4
239000003973 paint Substances 0.000 description 4
229920000647 polyepoxide Polymers 0.000 description 4
229920005862 polyol Polymers 0.000 description 4
150000003077 polyols Chemical class 0.000 description 4
239000007787 solid Substances 0.000 description 4
GZVHEAJQGPRDLQ-UHFFFAOYSA-N 6-phenyl-1,3,5-triazine-2,4-diamine Chemical compound NC1=NC(N)=NC(C=2C=CC=CC=2)=N1 GZVHEAJQGPRDLQ-UHFFFAOYSA-N 0.000 description 3
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
239000005057 Hexamethylene diisocyanate Substances 0.000 description 3
OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 3
DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
238000010521 absorption reaction Methods 0.000 description 3
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 3
125000004432 carbon atom Chemical group C* 0.000 description 3
MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
UAOMVDZJSHZZME-UHFFFAOYSA-N diisopropylamine Chemical compound CC(C)NC(C)C UAOMVDZJSHZZME-UHFFFAOYSA-N 0.000 description 3
RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 3
239000004922 lacquer Substances 0.000 description 3
238000004806 packaging method and process Methods 0.000 description 3
CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 description 3
VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 3
HXVNBWAKAOHACI-UHFFFAOYSA-N 2,4-dimethyl-3-pentanone Chemical compound CC(C)C(=O)C(C)C HXVNBWAKAOHACI-UHFFFAOYSA-N 0.000 description 2
HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 2
XLLIQLLCWZCATF-UHFFFAOYSA-N 2-methoxyethyl acetate Chemical compound COCCOC(C)=O XLLIQLLCWZCATF-UHFFFAOYSA-N 0.000 description 2
XTHFKEDIFFGKHM-UHFFFAOYSA-N Dimethoxyethane Chemical compound COCCOC XTHFKEDIFFGKHM-UHFFFAOYSA-N 0.000 description 2
VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
WOBHKFSMXKNTIM-UHFFFAOYSA-N Hydroxyethyl methacrylate Chemical compound CC(=C)C(=O)OCCO WOBHKFSMXKNTIM-UHFFFAOYSA-N 0.000 description 2
KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 2
OMOVVBIIQSXZSZ-UHFFFAOYSA-N [6-(4-acetyloxy-5,9a-dimethyl-2,7-dioxo-4,5a,6,9-tetrahydro-3h-pyrano[3,4-b]oxepin-5-yl)-5-formyloxy-3-(furan-3-yl)-3a-methyl-7-methylidene-1a,2,3,4,5,6-hexahydroindeno[1,7a-b]oxiren-4-yl] 2-hydroxy-3-methylpentanoate Chemical compound CC12C(OC(=O)C(O)C(C)CC)C(OC=O)C(C3(C)C(CC(=O)OC4(C)COC(=O)CC43)OC(C)=O)C(=C)C32OC3CC1C=1C=COC=1 OMOVVBIIQSXZSZ-UHFFFAOYSA-N 0.000 description 2
YRKCREAYFQTBPV-UHFFFAOYSA-N acetylacetone Chemical compound CC(=O)CC(C)=O YRKCREAYFQTBPV-UHFFFAOYSA-N 0.000 description 2
239000002253 acid Substances 0.000 description 2
230000000996 additive effect Effects 0.000 description 2
WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 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
125000003118 aryl group Chemical group 0.000 description 2
244000052616 bacterial pathogen Species 0.000 description 2
239000002981 blocking agent Substances 0.000 description 2
CDQSJQSWAWPGKG-UHFFFAOYSA-N butane-1,1-diol Chemical class CCCC(O)O CDQSJQSWAWPGKG-UHFFFAOYSA-N 0.000 description 2
UPIWXMRIPODGLE-UHFFFAOYSA-N butyl benzenecarboperoxoate Chemical group CCCCOOC(=O)C1=CC=CC=C1 UPIWXMRIPODGLE-UHFFFAOYSA-N 0.000 description 2
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 2
238000006243 chemical reaction Methods 0.000 description 2
150000001875 compounds Chemical class 0.000 description 2
229920001577 copolymer Polymers 0.000 description 2
239000003431 cross linking reagent Substances 0.000 description 2
NNBZCPXTIHJBJL-UHFFFAOYSA-N decalin Chemical compound C1CCCC2CCCCC21 NNBZCPXTIHJBJL-UHFFFAOYSA-N 0.000 description 2
JQVDAXLFBXTEQA-UHFFFAOYSA-N dibutylamine Chemical compound CCCCNCCCC JQVDAXLFBXTEQA-UHFFFAOYSA-N 0.000 description 2
125000005442 diisocyanate group Chemical group 0.000 description 2
WOZVHXUHUFLZGK-UHFFFAOYSA-N dimethyl terephthalate Chemical compound COC(=O)C1=CC=C(C(=O)OC)C=C1 WOZVHXUHUFLZGK-UHFFFAOYSA-N 0.000 description 2
238000005886 esterification reaction Methods 0.000 description 2
229920000578 graft copolymer Polymers 0.000 description 2
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 2
CATSNJVOTSVZJV-UHFFFAOYSA-N heptan-2-one Chemical compound CCCCCC(C)=O CATSNJVOTSVZJV-UHFFFAOYSA-N 0.000 description 2
239000003999 initiator Substances 0.000 description 2
IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 2
QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 2
VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 2
239000011976 maleic acid Substances 0.000 description 2
JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 2
229910052751 metal Inorganic materials 0.000 description 2
239000002184 metal Substances 0.000 description 2
239000000178 monomer Substances 0.000 description 2
SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 2
BDJRBEYXGGNYIS-UHFFFAOYSA-N nonanedioic acid Chemical compound OC(=O)CCCCCCCC(O)=O BDJRBEYXGGNYIS-UHFFFAOYSA-N 0.000 description 2
FDPIMTJIUBPUKL-UHFFFAOYSA-N pentan-3-one Chemical compound CCC(=O)CC FDPIMTJIUBPUKL-UHFFFAOYSA-N 0.000 description 2
XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 2
229920001296 polysiloxane Polymers 0.000 description 2
CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 2
239000000243 solution Substances 0.000 description 2
238000003756 stirring Methods 0.000 description 2
ARCGXLSVLAOJQL-UHFFFAOYSA-N trimellitic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C(C(O)=O)=C1 ARCGXLSVLAOJQL-UHFFFAOYSA-N 0.000 description 2
NMRPBPVERJPACX-UHFFFAOYSA-N (3S)-octan-3-ol Natural products CCCCCC(O)CC NMRPBPVERJPACX-UHFFFAOYSA-N 0.000 description 1
LZDKZFUFMNSQCJ-UHFFFAOYSA-N 1,2-diethoxyethane Chemical compound CCOCCOCC LZDKZFUFMNSQCJ-UHFFFAOYSA-N 0.000 description 1
PCHXZXKMYCGVFA-UHFFFAOYSA-N 1,3-diazetidine-2,4-dione Chemical compound O=C1NC(=O)N1 PCHXZXKMYCGVFA-UHFFFAOYSA-N 0.000 description 1
GDXHBFHOEYVPED-UHFFFAOYSA-N 1-(2-butoxyethoxy)butane Chemical compound CCCCOCCOCCCC GDXHBFHOEYVPED-UHFFFAOYSA-N 0.000 description 1
JLBXCKSMESLGTJ-UHFFFAOYSA-N 1-ethoxypropan-1-ol Chemical compound CCOC(O)CC JLBXCKSMESLGTJ-UHFFFAOYSA-N 0.000 description 1
RTBFRGCFXZNCOE-UHFFFAOYSA-N 1-methylsulfonylpiperidin-4-one Chemical compound CS(=O)(=O)N1CCC(=O)CC1 RTBFRGCFXZNCOE-UHFFFAOYSA-N 0.000 description 1
WAPNOHKVXSQRPX-UHFFFAOYSA-N 1-phenylethanol Chemical compound CC(O)C1=CC=CC=C1 WAPNOHKVXSQRPX-UHFFFAOYSA-N 0.000 description 1
SZSSMFVYZRQGIM-UHFFFAOYSA-N 2-(hydroxymethyl)-2-propylpropane-1,3-diol Chemical compound CCCC(CO)(CO)CO SZSSMFVYZRQGIM-UHFFFAOYSA-N 0.000 description 1
PTTPXKJBFFKCEK-UHFFFAOYSA-N 2-Methyl-4-heptanone Chemical compound CC(C)CC(=O)CC(C)C PTTPXKJBFFKCEK-UHFFFAOYSA-N 0.000 description 1
TXBCBTDQIULDIA-UHFFFAOYSA-N 2-[[3-hydroxy-2,2-bis(hydroxymethyl)propoxy]methyl]-2-(hydroxymethyl)propane-1,3-diol Chemical compound OCC(CO)(CO)COCC(CO)(CO)CO TXBCBTDQIULDIA-UHFFFAOYSA-N 0.000 description 1
SVONRAPFKPVNKG-UHFFFAOYSA-N 2-ethoxyethyl acetate Chemical compound CCOCCOC(C)=O SVONRAPFKPVNKG-UHFFFAOYSA-N 0.000 description 1
YIWUKEYIRIRTPP-UHFFFAOYSA-N 2-ethylhexan-1-ol Chemical compound CCCCC(CC)CO YIWUKEYIRIRTPP-UHFFFAOYSA-N 0.000 description 1
BNCADMBVWNPPIZ-UHFFFAOYSA-N 2-n,2-n,4-n,4-n,6-n,6-n-hexakis(methoxymethyl)-1,3,5-triazine-2,4,6-triamine Chemical compound COCN(COC)C1=NC(N(COC)COC)=NC(N(COC)COC)=N1 BNCADMBVWNPPIZ-UHFFFAOYSA-N 0.000 description 1
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239000004925 Acrylic resin Substances 0.000 description 1
229910000838 Al alloy Inorganic materials 0.000 description 1
WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 description 1
DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 1
241000254173 Coleoptera Species 0.000 description 1
229920003270 Cymel® Polymers 0.000 description 1
235000009161 Espostoa lanata Nutrition 0.000 description 1
240000001624 Espostoa lanata Species 0.000 description 1
239000005058 Isophorone diisocyanate Substances 0.000 description 1
229920003264 Maprenal® Polymers 0.000 description 1
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239000004721 Polyphenylene oxide Substances 0.000 description 1
239000004793 Polystyrene Substances 0.000 description 1
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ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 1
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238000005299 abrasion Methods 0.000 description 1
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238000007792 addition Methods 0.000 description 1
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235000011037 adipic acid Nutrition 0.000 description 1
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229940072049 amyl acetate Drugs 0.000 description 1
PGMYKACGEOXYJE-UHFFFAOYSA-N anhydrous amyl acetate Natural products CCCCCOC(C)=O PGMYKACGEOXYJE-UHFFFAOYSA-N 0.000 description 1
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239000007864 aqueous solution Substances 0.000 description 1
150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
239000000440 bentonite Substances 0.000 description 1
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235000019445 benzyl alcohol Nutrition 0.000 description 1
229960004217 benzyl alcohol Drugs 0.000 description 1
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125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
239000006229 carbon black Substances 0.000 description 1
150000001735 carboxylic acids Chemical class 0.000 description 1
239000007795 chemical reaction product Substances 0.000 description 1
125000002603 chloroethyl group Chemical group [H]C([*])([H])C([H])([H])Cl 0.000 description 1
239000003086 colorant Substances 0.000 description 1
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HPXRVTGHNJAIIH-UHFFFAOYSA-N cyclohexanol Chemical compound OC1CCCCC1 HPXRVTGHNJAIIH-UHFFFAOYSA-N 0.000 description 1
XCIXKGXIYUWCLL-UHFFFAOYSA-N cyclopentanol Chemical compound OC1CCCC1 XCIXKGXIYUWCLL-UHFFFAOYSA-N 0.000 description 1
125000002704 decyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
239000013530 defoamer Substances 0.000 description 1
125000006159 dianhydride group Chemical group 0.000 description 1
235000014113 dietary fatty acids Nutrition 0.000 description 1
229940043279 diisopropylamine Drugs 0.000 description 1
239000000539 dimer Substances 0.000 description 1
150000002009 diols Chemical class 0.000 description 1
239000006185 dispersion Substances 0.000 description 1
239000012153 distilled water Substances 0.000 description 1
LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 1
230000000694 effects Effects 0.000 description 1
230000032050 esterification Effects 0.000 description 1
150000002170 ethers Chemical class 0.000 description 1
229940093499 ethyl acetate Drugs 0.000 description 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
239000004744 fabric Substances 0.000 description 1
239000000194 fatty acid Substances 0.000 description 1
229930195729 fatty acid Natural products 0.000 description 1
150000004665 fatty acids Chemical class 0.000 description 1
239000000945 filler Substances 0.000 description 1
238000011049 filling Methods 0.000 description 1
239000001530 fumaric acid Substances 0.000 description 1
235000011187 glycerol Nutrition 0.000 description 1
238000010438 heat treatment Methods 0.000 description 1
NGAZZOYFWWSOGK-UHFFFAOYSA-N heptan-3-one Chemical compound CCCCC(=O)CC NGAZZOYFWWSOGK-UHFFFAOYSA-N 0.000 description 1
MNWFXJYAOYHMED-UHFFFAOYSA-M heptanoate Chemical compound CCCCCCC([O-])=O MNWFXJYAOYHMED-UHFFFAOYSA-M 0.000 description 1
ACCCMOQWYVYDOT-UHFFFAOYSA-N hexane-1,1-diol Chemical class CCCCCC(O)O ACCCMOQWYVYDOT-UHFFFAOYSA-N 0.000 description 1
FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 1
125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
UQSXHKLRYXJYBZ-UHFFFAOYSA-N iron oxide Inorganic materials [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 1
235000013980 iron oxide Nutrition 0.000 description 1
VBMVTYDPPZVILR-UHFFFAOYSA-N iron(2+);oxygen(2-) Chemical class [O-2].[Fe+2] VBMVTYDPPZVILR-UHFFFAOYSA-N 0.000 description 1
239000012948 isocyanate Substances 0.000 description 1
150000002513 isocyanates Chemical class 0.000 description 1
ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Chemical compound OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 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
150000002576 ketones Chemical class 0.000 description 1
230000007774 longterm Effects 0.000 description 1
239000000463 material Substances 0.000 description 1
FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical compound CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 description 1
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
238000002156 mixing Methods 0.000 description 1
YKYONYBAUNKHLG-UHFFFAOYSA-N n-Propyl acetate Natural products CCCOC(C)=O YKYONYBAUNKHLG-UHFFFAOYSA-N 0.000 description 1
WHIVNJATOVLWBW-UHFFFAOYSA-N n-butan-2-ylidenehydroxylamine Chemical compound CCC(C)=NO WHIVNJATOVLWBW-UHFFFAOYSA-N 0.000 description 1
125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
229940117969 neopentyl glycol Drugs 0.000 description 1
230000006855 networking Effects 0.000 description 1
125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
150000002923 oximes Chemical class 0.000 description 1
WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
UWJJYHHHVWZFEP-UHFFFAOYSA-N pentane-1,1-diol Chemical class CCCCC(O)O UWJJYHHHVWZFEP-UHFFFAOYSA-N 0.000 description 1
125000000864 peroxy group Chemical group O(O*)* 0.000 description 1
229920001568 phenolic resin Polymers 0.000 description 1
239000013034 phenoxy resin Substances 0.000 description 1
229920006287 phenoxy resin Polymers 0.000 description 1
239000004014 plasticizer Substances 0.000 description 1
229920001610 polycaprolactone Polymers 0.000 description 1
239000004632 polycaprolactone Substances 0.000 description 1
229920000570 polyether Polymers 0.000 description 1
229920001223 polyethylene glycol Polymers 0.000 description 1
229940068918 polyethylene glycol 400 Drugs 0.000 description 1
229920002223 polystyrene Polymers 0.000 description 1
230000008092 positive effect Effects 0.000 description 1
125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical compound C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 description 1
ULWHHBHJGPPBCO-UHFFFAOYSA-N propane-1,1-diol Chemical compound CCC(O)O ULWHHBHJGPPBCO-UHFFFAOYSA-N 0.000 description 1
229940090181 propyl acetate Drugs 0.000 description 1
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
239000011253 protective coating Substances 0.000 description 1
238000007493 shaping process Methods 0.000 description 1
235000015096 spirit Nutrition 0.000 description 1
239000003381 stabilizer Substances 0.000 description 1
239000010959 steel Substances 0.000 description 1
239000000758 substrate Substances 0.000 description 1
210000004243 sweat Anatomy 0.000 description 1
GJBRNHKUVLOCEB-UHFFFAOYSA-N tert-butyl benzenecarboperoxoate Chemical compound CC(C)(C)OOC(=O)C1=CC=CC=C1 GJBRNHKUVLOCEB-UHFFFAOYSA-N 0.000 description 1
150000000000 tetracarboxylic acids Chemical class 0.000 description 1
UFDHBDMSHIXOKF-UHFFFAOYSA-N tetrahydrophthalic acid Natural products OC(=O)C1=C(C(O)=O)CCCC1 UFDHBDMSHIXOKF-UHFFFAOYSA-N 0.000 description 1
DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 description 1
LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 description 1
150000003628 tricarboxylic acids Chemical class 0.000 description 1
SRPWOOOHEPICQU-UHFFFAOYSA-N trimellitic anhydride Chemical compound OC(=O)C1=CC=C2C(=O)OC(=O)C2=C1 SRPWOOOHEPICQU-UHFFFAOYSA-N 0.000 description 1
239000013638 trimer Substances 0.000 description 1
QXJQHYBHAIHNGG-UHFFFAOYSA-N trimethylolethane Chemical compound OCC(C)(CO)CO QXJQHYBHAIHNGG-UHFFFAOYSA-N 0.000 description 1
150000004072 triols Chemical class 0.000 description 1
AVWRKZWQTYIKIY-UHFFFAOYSA-N urea-1-carboxylic acid Chemical group NC(=O)NC(O)=O AVWRKZWQTYIKIY-UHFFFAOYSA-N 0.000 description 1
NQPDZGIKBAWPEJ-UHFFFAOYSA-N valeric acid Chemical compound CCCCC(O)=O NQPDZGIKBAWPEJ-UHFFFAOYSA-N 0.000 description 1
239000002966 varnish Substances 0.000 description 1
PXXNTAGJWPJAGM-UHFFFAOYSA-N vertaline Natural products C1C2C=3C=C(OC)C(OC)=CC=3OC(C=C3)=CC=C3CCC(=O)OC1CC1N2CCCC1 PXXNTAGJWPJAGM-UHFFFAOYSA-N 0.000 description 1
239000008096 xylene Substances 0.000 description 1

Classifications

- 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
- C09D175/00—Coating compositions based on polyureas or polyurethanes; Coating compositions based on derivatives of such polymers
- C09D175/04—Polyurethanes
- C09D175/06—Polyurethanes from polyesters
- 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
- C09D167/00—Coating compositions based on polyesters obtained by reactions forming a carboxylic ester link in the main chain; Coating compositions based on derivatives of such polymers
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/40—High-molecular-weight compounds
- C08G18/62—Polymers of compounds having carbon-to-carbon double bonds
- C08G18/6216—Polymers of alpha-beta ethylenically unsaturated carboxylic acids or of derivatives thereof
- C08G18/625—Polymers of alpha-beta ethylenically unsaturated carboxylic acids; hydrolyzed polymers of esters of these acids
- C08G18/6254—Polymers of alpha-beta ethylenically unsaturated carboxylic acids and of esters of these acids containing hydroxy groups
- 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
- C09D133/00—Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Coating compositions based on derivatives of such polymers
- C09D133/04—Homopolymers or copolymers of esters
- C09D133/06—Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, the oxygen atom being present only as part of the carboxyl radical
- 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
- C09D133/00—Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Coating compositions based on derivatives of such polymers
- C09D133/04—Homopolymers or copolymers of esters
- C09D133/06—Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, the oxygen atom being present only as part of the carboxyl radical
- C09D133/062—Copolymers with monomers not covered by C09D133/06
- C09D133/066—Copolymers with monomers not covered by C09D133/06 containing -OH groups
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L75/00—Compositions of polyureas or polyurethanes; Compositions of derivatives of such polymers
- C08L75/04—Polyurethanes

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Life Sciences & Earth Sciences (AREA)
Engineering & Computer Science (AREA)
Materials Engineering (AREA)
Wood Science & Technology (AREA)
Chemical Kinetics & Catalysis (AREA)
Health & Medical Sciences (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Paints Or Removers (AREA)

DE19703091A 1997-01-29 1997-01-29 Überzugsmittel für Nahrungsmittelbehälter Ceased DE19703091A1 (de)

Priority Applications (7)

Application Number	Priority Date	Filing Date	Title
DE19703091A DE19703091A1 (de)	1997-01-29	1997-01-29	Überzugsmittel für Nahrungsmittelbehälter
AU57560/98A AU5756098A (en)	1997-01-29	1997-12-10	Coating composition for food containers
KR1019997006854A KR20000070606A (ko)	1997-01-29	1997-12-10	식품 용기용 피복제 조성물
PCT/EP1997/006906 WO1998032807A1 (fr)	1997-01-29	1997-12-10	Composition de revêtement pour des recipients alimentaires
EP97953778A EP0956321A1 (fr)	1997-01-29	1997-12-10	Composition de rev tement pour des recipients alimentaires
BR9714327-8A BR9714327A (pt)	1997-01-29	1997-12-10	Composição de revestimento para recipientes de alimento
CA002278351A CA2278351A1 (fr)	1997-01-29	1997-12-10	Composition de revetement pour des recipients alimentaires

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE19703091A DE19703091A1 (de)	1997-01-29	1997-01-29	Überzugsmittel für Nahrungsmittelbehälter

Publications (1)

Publication Number	Publication Date
DE19703091A1 true DE19703091A1 (de)	1998-07-30

Family

ID=7818607

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DE19703091A Ceased DE19703091A1 (de)	1997-01-29	1997-01-29	Überzugsmittel für Nahrungsmittelbehälter

Country Status (7)

Country	Link
EP (1)	EP0956321A1 (fr)
KR (1)	KR20000070606A (fr)
AU (1)	AU5756098A (fr)
BR (1)	BR9714327A (fr)
CA (1)	CA2278351A1 (fr)
DE (1)	DE19703091A1 (fr)
WO (1)	WO1998032807A1 (fr)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
EP1672041A1 (fr) *	2004-12-17	2006-06-21	Bayer MaterialScience AG	Revêtements pour un récipient alimentaire

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE10349811A1 (de) *	2003-10-24	2005-05-25	Bayer Materialscience Ag	Beschichtungen für Nahrungsmittelbehälter
EP2419483B1 (fr)	2009-04-13	2014-08-27	W.R. Grace & Co.-Conn.	Revetement resistant a un traitement a ph eleve pour les contenants alimentaires metalliques
CN109423129B (zh) *	2017-06-21	2020-08-28	广东华润涂料有限公司	适用于在三片罐上形成侧缝条或侧缝涂层的水性涂料组合物

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DE2507884A1 (de) *	1975-02-24	1976-09-02	Basf Ag	Waessrige ueberzugsmittel
EP0006336B1 (fr) *	1978-06-12	1982-08-11	Mobil Oil Corporation	Composition d'enduction sous forme d'émulsion aqueuse à base de mélanges auto-émulsifiables estérifiés de polyépoxydes et de copolymères
US4847316A (en) *	1987-05-06	1989-07-11	Eastman Kodak Company	Aqueous dispersion blends of polyesters and polyurethane materials and printing inks therefrom
WO1990000283A1 (fr) *	1988-07-04	1990-01-11	Swedish Institute Of Computer Science	Systeme multiprocesseur pourvu d'un systeme d'antememoire hierarchique
EP0358979B1 (fr) *	1988-09-01	1992-06-17	Bayer Ag	Masses de revêtement, leur procédé de préparation et utilisation de systèmes sélectionnés de polyuréthane à deux composants comme liant pour de telles masses de revêtement
DE4332015A1 (de) *	1993-09-21	1995-03-23	Basf Lacke & Farben	Verfahren zur Herstellung von Decklackschichten
DE4421823A1 (de) *	1994-06-22	1996-01-04	Basf Lacke & Farben	Aus mindestens 3 Komponenten bestehendes Beschichtungsmittel, Verfahren zu seiner Herstellung sowie seine Verwendung

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US4395444A (en) *	1981-09-25	1983-07-26	Ppg Industries, Inc.	Thermosetting cationic acrylic latex compositions containing blocked isocyanates
JPH0372577A (ja) *	1989-04-28	1991-03-27	Toyo Ink Mfg Co Ltd	水性塗料組成物
US5314945A (en) *	1990-12-03	1994-05-24	E. I. Du Pont De Nemours And Company	Waterbased coating compositions of methylol(meth)acrylamide acrylic polymer, polyurethane and melamine crosslinking agent
DE4223183C1 (en) *	1992-07-15	1993-07-15	Herberts Gmbh, 5600 Wuppertal, De	Emulsifier-free thermo-curable coating as aq. emulsion - comprises self-emulsifying ester-based copolymers, polyester oligomers, water-(in)soluble amine resin crosslinking agents and capped poly:isocyanate(s)
JPH0641491A (ja) *	1992-07-23	1994-02-15	Kansai Paint Co Ltd	水性塗料とその塗装方法
JPH08209066A (ja) *	1995-02-07	1996-08-13	Kansai Paint Co Ltd	水性中塗塗料

1997
- 1997-01-29 DE DE19703091A patent/DE19703091A1/de not_active Ceased
- 1997-12-10 BR BR9714327-8A patent/BR9714327A/pt not_active Application Discontinuation
- 1997-12-10 WO PCT/EP1997/006906 patent/WO1998032807A1/fr not_active Ceased
- 1997-12-10 AU AU57560/98A patent/AU5756098A/en not_active Abandoned
- 1997-12-10 KR KR1019997006854A patent/KR20000070606A/ko not_active Withdrawn
- 1997-12-10 CA CA002278351A patent/CA2278351A1/fr not_active Abandoned
- 1997-12-10 EP EP97953778A patent/EP0956321A1/fr not_active Withdrawn

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DE2507884A1 (de) *	1975-02-24	1976-09-02	Basf Ag	Waessrige ueberzugsmittel
EP0006336B1 (fr) *	1978-06-12	1982-08-11	Mobil Oil Corporation	Composition d'enduction sous forme d'émulsion aqueuse à base de mélanges auto-émulsifiables estérifiés de polyépoxydes et de copolymères
US4847316A (en) *	1987-05-06	1989-07-11	Eastman Kodak Company	Aqueous dispersion blends of polyesters and polyurethane materials and printing inks therefrom
WO1990000283A1 (fr) *	1988-07-04	1990-01-11	Swedish Institute Of Computer Science	Systeme multiprocesseur pourvu d'un systeme d'antememoire hierarchique
EP0358979B1 (fr) *	1988-09-01	1992-06-17	Bayer Ag	Masses de revêtement, leur procédé de préparation et utilisation de systèmes sélectionnés de polyuréthane à deux composants comme liant pour de telles masses de revêtement
DE4332015A1 (de) *	1993-09-21	1995-03-23	Basf Lacke & Farben	Verfahren zur Herstellung von Decklackschichten
DE4421823A1 (de) *	1994-06-22	1996-01-04	Basf Lacke & Farben	Aus mindestens 3 Komponenten bestehendes Beschichtungsmittel, Verfahren zu seiner Herstellung sowie seine Verwendung

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* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
EP1672041A1 (fr) *	2004-12-17	2006-06-21	Bayer MaterialScience AG	Revêtements pour un récipient alimentaire

Also Published As

Publication number	Publication date
EP0956321A1 (fr)	1999-11-17
WO1998032807A1 (fr)	1998-07-30
CA2278351A1 (fr)	1998-07-30
BR9714327A (pt)	2000-02-08
AU5756098A (en)	1998-08-18
KR20000070606A (ko)	2000-11-25

Publication	Publication Date	Title
EP0579193B1 (fr)	1999-01-13	Composition de revêtement aqueuse thermodurcissable, sa préparation et utilisation
EP0947557B1 (fr)	2007-12-05	Dispersions de copolymères, combinaisons de liant à base de dispersions de copolymères, procédé de leur fabrication et leur utilisation
EP1024184B1 (fr)	2005-08-10	Composition de revêtement aqueuse, procédé de fabrication et d'utilisation correspondants
DE69705199T2 (de)	2001-11-08	Wässrige bindemittelzusammensetzung und deren verwendung
DE3210051A1 (de)	1983-09-29	Wasserverduennbares ueberzugsmittel zur herstellung der basisschicht eines mehrschichtueberzuges
DE69302863T2 (de)	1996-10-24	Wässrige Beschichtungszusammensetzung und diese verwendendes Beschichtungsverfahren
EP0363723A1 (fr)	1990-04-18	Procédé de préparation d'un revêtement multicouche, compositions de revêtement aqueuses, résines acryliques diluables dans l'eau et procédé de préparation de résines acryliques diluables dans l'eau
DE4009858A1 (de)	1991-10-02	Verfahren zur herstellung einer mehrschichtigen lackierung und fuer dieses verfahren geeignete waessrige basislacke
EP0610450B1 (fr)	2003-06-04	Vernis, procede pour sa fabrication et son utilisation
EP1490448B1 (fr)	2007-05-30	Systemes pur a deux composantes aqueux
EP0819710B1 (fr)	2001-10-24	Nouveaux systèmes de liants a haute teneur en solide a base de polyurethanne à deux composants
EP0330139A2 (fr)	1989-08-30	Utilisation d'un matériau de revêtement pour préparer des revêtements anti-impacts et/ou des couches de mastic
EP0705853B1 (fr)	1999-02-03	Copolymères avec des monomères cycliques ou polycycliques avec une répartition spéciale d'isomères et leur usage dans des revêtements
DE2507842A1 (de)	1976-09-02	Waessrige ueberzugsmittel
EP0365775B1 (fr)	1993-03-03	Procédé de préparation d'une revêtement multicouche par utilisation de compositions de revêtement aqueux
EP0324334B1 (fr)	1991-10-09	Liants diluables dans l'eau, un procédé pour leur préparation et leur utilisation
AT409633B (de)	2002-09-25	Bindemittel für ''soft-feel''-lacke
EP0778298B1 (fr)	2001-04-18	Combinaison liante à haute teneur en solides
DE19705219A1 (de)	1998-08-13	Universell einsetzbare Pigmentpasten und ihre Verwendung zur Herstellung von wäßrigen Lacken
DE60116862T2 (de)	2006-10-19	Verfahren zur bereitung einer pulvrlackzusammensetzung, pulverlackzusammensetzung und verfahren zur bildung des beschichtungsfilms
DE2507884A1 (de)	1976-09-02	Waessrige ueberzugsmittel
DE2854989C3 (de)	1981-02-05	Pulverüberzugspräparat
DE2539104C3 (de)	1986-07-10	Lösungsmittelarme Einbrennlacke
EP0605494B1 (fr)	1996-02-07	Procede de production d'une composition de revetement aqueuse
DE19703091A1 (de)	1998-07-30	Überzugsmittel für Nahrungsmittelbehälter

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Date	Code	Title	Description
1998-07-30	OP8	Request for examination as to paragraph 44 patent law
1999-09-30	8127	New person/name/address of the applicant	Owner name: PPG INDUSTRIES OHIO, INC., CLEVELAND, OHIO, US
2000-11-30	8131	Rejection

DE19703091A1 - Überzugsmittel für Nahrungsmittelbehälter - Google Patents

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