CA1102036A - Compose d'enduction a forte teneur en solides - Google Patents

Compose d'enduction a forte teneur en solides

Info

Publication number: CA1102036A
Authority: CA; Canada
Prior art keywords: weight; coating composition; parts; solids coating; further characterized
Prior art date: 1978-01-27
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

CA295,836A

Other languages

English (en)

Inventor

William J. Yapp

Robert E. Mcdonald

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.)

Sherwin Williams Co

Original Assignee

Sherwin Williams Co

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.)

1978-01-27

Filing date

1978-01-27

Publication date

1981-05-26

1978-01-27 Application filed by Sherwin Williams Co filed Critical Sherwin Williams Co

1978-01-27 Priority to CA295,836A priority Critical patent/CA1102036A/fr

1981-05-26 Application granted granted Critical

1981-05-26 Publication of CA1102036A publication Critical patent/CA1102036A/fr

Status Expired legal-status Critical Current

Links

239000008199 coating composition Substances 0.000 title claims abstract description 39
239000007787 solid Substances 0.000 title claims abstract description 37
-1 alkoxy alkyl melamine Chemical compound 0.000 claims abstract description 60
229920000728 polyester Polymers 0.000 claims abstract description 37
238000000576 coating method Methods 0.000 claims abstract description 34
239000003431 cross linking reagent Substances 0.000 claims abstract description 31
125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract description 31
239000011248 coating agent Substances 0.000 claims abstract description 25
239000012948 isocyanate Substances 0.000 claims abstract description 25
229920000647 polyepoxide Polymers 0.000 claims abstract description 24
239000003822 epoxy resin Substances 0.000 claims abstract description 23
150000002513 isocyanates Chemical class 0.000 claims abstract description 22
239000007859 condensation product Substances 0.000 claims abstract description 21
229920000877 Melamine resin Polymers 0.000 claims abstract description 15
239000000203 mixture Substances 0.000 claims description 41
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 38
239000002253 acid Substances 0.000 claims description 22
239000000758 substrate Substances 0.000 claims description 18
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 17
XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims description 17
XXROGKLTLUQVRX-UHFFFAOYSA-N allyl alcohol Chemical compound OCC=C XXROGKLTLUQVRX-UHFFFAOYSA-N 0.000 claims description 16
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WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 claims description 12
GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 claims description 12
238000000034 method Methods 0.000 claims description 12
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125000001931 aliphatic group Chemical group 0.000 claims description 11
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125000004432 carbon atom Chemical group C* 0.000 claims description 10
QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 claims description 10
JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 claims description 10
150000003440 styrenes Chemical class 0.000 claims description 10
KFVIYKFKUYBKTP-UHFFFAOYSA-N 2-n-(methoxymethyl)-1,3,5-triazine-2,4,6-triamine Chemical group COCNC1=NC(N)=NC(N)=N1 KFVIYKFKUYBKTP-UHFFFAOYSA-N 0.000 claims description 9
WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 claims description 9
150000008064 anhydrides Chemical class 0.000 claims description 9
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OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims description 5
239000001361 adipic acid Substances 0.000 claims description 5
235000011037 adipic acid Nutrition 0.000 claims description 5
150000005846 sugar alcohols Polymers 0.000 claims description 5
125000004849 alkoxymethyl group Chemical group 0.000 claims description 4
239000004408 titanium dioxide Substances 0.000 claims description 4
238000009833 condensation Methods 0.000 claims description 3
230000005494 condensation Effects 0.000 claims description 3
239000000047 product Substances 0.000 claims description 3
125000003545 alkoxy group Chemical group 0.000 claims description 2
229920006305 unsaturated polyester Polymers 0.000 claims description 2
125000002485 formyl group Chemical class [H]C(*)=O 0.000 claims 4
239000001023 inorganic pigment Substances 0.000 claims 2
CTRPRMNBTVRDFH-UHFFFAOYSA-N 2-n-methyl-1,3,5-triazine-2,4,6-triamine Chemical compound CNC1=NC(N)=NC(N)=N1 CTRPRMNBTVRDFH-UHFFFAOYSA-N 0.000 claims 1
NPLRPKYYUCHQBF-UHFFFAOYSA-N C=Cc1ccccc1.OCCCOC(=O)C=C Chemical group C=Cc1ccccc1.OCCCOC(=O)C=C NPLRPKYYUCHQBF-UHFFFAOYSA-N 0.000 claims 1
125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract description 7
235000019441 ethanol Nutrition 0.000 description 17
239000002904 solvent Substances 0.000 description 14
239000003054 catalyst Substances 0.000 description 13
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 9
150000001299 aldehydes Chemical class 0.000 description 9
125000000217 alkyl group Chemical group 0.000 description 9
235000013877 carbamide Nutrition 0.000 description 9
239000003795 chemical substances by application Substances 0.000 description 7
229940091868 melamine Drugs 0.000 description 7
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
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238000006243 chemical reaction Methods 0.000 description 5
KUBDPQJOLOUJRM-UHFFFAOYSA-N 2-(chloromethyl)oxirane;4-[2-(4-hydroxyphenyl)propan-2-yl]phenol Chemical compound ClCC1CO1.C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 KUBDPQJOLOUJRM-UHFFFAOYSA-N 0.000 description 4
150000001252 acrylic acid derivatives Chemical class 0.000 description 4
239000002981 blocking agent Substances 0.000 description 4
150000001735 carboxylic acids Chemical class 0.000 description 4
238000007796 conventional method Methods 0.000 description 4
150000002148 esters Chemical class 0.000 description 4
229910052751 metal Inorganic materials 0.000 description 4
239000002184 metal Substances 0.000 description 4
ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 3
150000001412 amines Chemical class 0.000 description 3
MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
150000002978 peroxides Chemical class 0.000 description 3
229920005862 polyol Polymers 0.000 description 3
229920001296 polysiloxane Polymers 0.000 description 3
239000000376 reactant Substances 0.000 description 3
229910052708 sodium Inorganic materials 0.000 description 3
239000011734 sodium Substances 0.000 description 3
239000007921 spray Substances 0.000 description 3
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 3
QQOWHRYOXYEMTL-UHFFFAOYSA-N triazin-4-amine Chemical compound N=C1C=CN=NN1 QQOWHRYOXYEMTL-UHFFFAOYSA-N 0.000 description 3
HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 2
MZGMQAMKOBOIDR-UHFFFAOYSA-N 2-[2-(2-hydroxyethoxy)ethoxy]ethyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCOCCOCCO MZGMQAMKOBOIDR-UHFFFAOYSA-N 0.000 description 2
QUASZQPLPKGIJY-UHFFFAOYSA-N 2-[2-[2-(2-hydroxyethoxy)ethoxy]ethoxy]ethyl prop-2-enoate Chemical compound OCCOCCOCCOCCOC(=O)C=C QUASZQPLPKGIJY-UHFFFAOYSA-N 0.000 description 2
ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 description 2
QUTLXFKECHNPNF-UHFFFAOYSA-N 2-hydroxybutyl 3-chloro-2-methylprop-2-enoate Chemical compound CCC(O)COC(=O)C(C)=CCl QUTLXFKECHNPNF-UHFFFAOYSA-N 0.000 description 2
WXUAQHNMJWJLTG-UHFFFAOYSA-N 2-methylbutanedioic acid Chemical compound OC(=O)C(C)CC(O)=O WXUAQHNMJWJLTG-UHFFFAOYSA-N 0.000 description 2
DXIJHCSGLOHNES-UHFFFAOYSA-N 3,3-dimethylbut-1-enylbenzene Chemical compound CC(C)(C)C=CC1=CC=CC=C1 DXIJHCSGLOHNES-UHFFFAOYSA-N 0.000 description 2
JRCGLALFKDKSAN-UHFFFAOYSA-N 3-hydroxybutyl prop-2-enoate Chemical compound CC(O)CCOC(=O)C=C JRCGLALFKDKSAN-UHFFFAOYSA-N 0.000 description 2
QOXOZONBQWIKDA-UHFFFAOYSA-N 3-hydroxypropyl Chemical group [CH2]CCO QOXOZONBQWIKDA-UHFFFAOYSA-N 0.000 description 2
LSYDHHZEYRXMGP-UHFFFAOYSA-N 3-hydroxypropyl 2-chloroprop-2-enoate Chemical compound OCCCOC(=O)C(Cl)=C LSYDHHZEYRXMGP-UHFFFAOYSA-N 0.000 description 2
SXIFAEWFOJETOA-UHFFFAOYSA-N 4-hydroxy-butyl Chemical group [CH2]CCCO SXIFAEWFOJETOA-UHFFFAOYSA-N 0.000 description 2
INRQKLGGIVSJRR-UHFFFAOYSA-N 5-hydroxypentyl prop-2-enoate Chemical compound OCCCCCOC(=O)C=C INRQKLGGIVSJRR-UHFFFAOYSA-N 0.000 description 2
HGINCPLSRVDWNT-UHFFFAOYSA-N Acrolein Chemical compound C=CC=O HGINCPLSRVDWNT-UHFFFAOYSA-N 0.000 description 2
FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Chemical compound CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 description 2
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical group [Cl] ZAMOUSCENKQFHK-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
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-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
LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 2
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APZPSKFMSWZPKL-UHFFFAOYSA-N [3-hydroxy-2,2-bis(hydroxymethyl)propyl] 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCC(CO)(CO)CO APZPSKFMSWZPKL-UHFFFAOYSA-N 0.000 description 2
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238000000889 atomisation Methods 0.000 description 2
HUMNYLRZRPPJDN-UHFFFAOYSA-N benzaldehyde Chemical compound O=CC1=CC=CC=C1 HUMNYLRZRPPJDN-UHFFFAOYSA-N 0.000 description 2
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229910052794 bromium Chemical group 0.000 description 2
239000000460 chlorine Substances 0.000 description 2
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238000004132 cross linking Methods 0.000 description 2
PFURGBBHAOXLIO-UHFFFAOYSA-N cyclohexane-1,2-diol Chemical compound OC1CCCCC1O PFURGBBHAOXLIO-UHFFFAOYSA-N 0.000 description 2
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JGFBRKRYDCGYKD-UHFFFAOYSA-N dibutyl(oxo)tin Chemical compound CCCC[Sn](=O)CCCC JGFBRKRYDCGYKD-UHFFFAOYSA-N 0.000 description 2
KWABLUYIOFEZOY-UHFFFAOYSA-N dioctyl butanedioate Chemical compound CCCCCCCCOC(=O)CCC(=O)OCCCCCCCC KWABLUYIOFEZOY-UHFFFAOYSA-N 0.000 description 2
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150000002170 ethers Chemical class 0.000 description 2
HOXINJBQVZWYGZ-UHFFFAOYSA-N fenbutatin oxide Chemical compound C=1C=CC=CC=1C(C)(C)C[Sn](O[Sn](CC(C)(C)C=1C=CC=CC=1)(CC(C)(C)C=1C=CC=CC=1)CC(C)(C)C=1C=CC=CC=1)(CC(C)(C)C=1C=CC=CC=1)CC(C)(C)C1=CC=CC=C1 HOXINJBQVZWYGZ-UHFFFAOYSA-N 0.000 description 2
125000000524 functional group Chemical group 0.000 description 2
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238000010438 heat treatment Methods 0.000 description 2
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150000002430 hydrocarbons Chemical class 0.000 description 2
239000001257 hydrogen Substances 0.000 description 2
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238000011065 in-situ storage Methods 0.000 description 2
150000002576 ketones Chemical class 0.000 description 2
239000000463 material Substances 0.000 description 2
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150000003839 salts Chemical class 0.000 description 2
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JCTXKRPTIMZBJT-UHFFFAOYSA-N 2,2,4-trimethylpentane-1,3-diol Chemical compound CC(C)C(O)C(C)(C)CO JCTXKRPTIMZBJT-UHFFFAOYSA-N 0.000 description 1
HGOUNPXIJSDIKV-UHFFFAOYSA-N 2,2-bis(hydroxymethyl)butyl 2-methylprop-2-enoate Chemical compound CCC(CO)(CO)COC(=O)C(C)=C HGOUNPXIJSDIKV-UHFFFAOYSA-N 0.000 description 1
SYENVBKSVVOOPS-UHFFFAOYSA-N 2,2-bis(hydroxymethyl)butyl prop-2-enoate Chemical compound CCC(CO)(CO)COC(=O)C=C SYENVBKSVVOOPS-UHFFFAOYSA-N 0.000 description 1
HQOVXPHOJANJBR-UHFFFAOYSA-N 2,2-bis(tert-butylperoxy)butane Chemical compound CC(C)(C)OOC(C)(CC)OOC(C)(C)C HQOVXPHOJANJBR-UHFFFAOYSA-N 0.000 description 1
BTUDGPVTCYNYLK-UHFFFAOYSA-N 2,2-dimethylglutaric acid Chemical compound OC(=O)C(C)(C)CCC(O)=O BTUDGPVTCYNYLK-UHFFFAOYSA-N 0.000 description 1
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GWYFCOCPABKNJV-UHFFFAOYSA-N isovaleric acid Chemical compound CC(C)CC(O)=O GWYFCOCPABKNJV-UHFFFAOYSA-N 0.000 description 1
239000004922 lacquer Substances 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
238000005259 measurement Methods 0.000 description 1
150000007974 melamines Chemical class 0.000 description 1
238000002844 melting Methods 0.000 description 1
230000008018 melting Effects 0.000 description 1
150000002734 metacrylic acid derivatives Chemical class 0.000 description 1
229910044991 metal oxide Inorganic materials 0.000 description 1
150000004706 metal oxides Chemical class 0.000 description 1
229940063557 methacrylate Drugs 0.000 description 1
UZKWTJUDCOPSNM-UHFFFAOYSA-N methoxybenzene Substances CCCCOC=C UZKWTJUDCOPSNM-UHFFFAOYSA-N 0.000 description 1
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
229940043265 methyl isobutyl ketone Drugs 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
229940032007 methylethyl ketone Drugs 0.000 description 1
150000007522 mineralic acids Chemical class 0.000 description 1
238000012986 modification Methods 0.000 description 1
230000004048 modification Effects 0.000 description 1
WHIVNJATOVLWBW-UHFFFAOYSA-N n-butan-2-ylidenehydroxylamine Chemical compound CCC(C)=NO WHIVNJATOVLWBW-UHFFFAOYSA-N 0.000 description 1
DIOQZVSQGTUSAI-UHFFFAOYSA-N n-butylhexane Natural products CCCCCCCCCC DIOQZVSQGTUSAI-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
ZCYXXKJEDCHMGH-UHFFFAOYSA-N nonane Chemical compound CCCC[CH]CCCC ZCYXXKJEDCHMGH-UHFFFAOYSA-N 0.000 description 1
BKIMMITUMNQMOS-UHFFFAOYSA-N normal nonane Natural products CCCCCCCCC BKIMMITUMNQMOS-UHFFFAOYSA-N 0.000 description 1
ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
235000005985 organic acids Nutrition 0.000 description 1
150000001451 organic peroxides Chemical class 0.000 description 1
150000002923 oximes Chemical class 0.000 description 1
150000002924 oxiranes Chemical class 0.000 description 1
125000000864 peroxy group Chemical group O(O*)* 0.000 description 1
229920001223 polyethylene glycol Polymers 0.000 description 1
239000000843 powder Substances 0.000 description 1
238000002360 preparation method Methods 0.000 description 1
239000001294 propane Substances 0.000 description 1
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
230000005855 radiation Effects 0.000 description 1
229920005989 resin Polymers 0.000 description 1
239000011347 resin Substances 0.000 description 1
230000002441 reversible effect Effects 0.000 description 1
229920006395 saturated elastomer Polymers 0.000 description 1
239000000600 sorbitol Substances 0.000 description 1
229920001909 styrene-acrylic polymer Polymers 0.000 description 1
150000003460 sulfonic acids Chemical class 0.000 description 1
239000004094 surface-active agent Substances 0.000 description 1
150000003568 thioethers Chemical class 0.000 description 1
ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
229920002554 vinyl polymer Polymers 0.000 description 1
238000005406 washing Methods 0.000 description 1
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
239000000080 wetting agent Substances 0.000 description 1
239000011787 zinc oxide Substances 0.000 description 1

Landscapes

Paints Or Removers (AREA)

CA295,836A 1978-01-27 1978-01-27 Compose d'enduction a forte teneur en solides Expired CA1102036A (fr)

Priority Applications (1)

Application Number	Priority Date	Filing Date	Title
CA295,836A CA1102036A (fr)	1978-01-27	1978-01-27	Compose d'enduction a forte teneur en solides

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
CA295,836A CA1102036A (fr)	1978-01-27	1978-01-27	Compose d'enduction a forte teneur en solides

Publications (1)

Publication Number	Publication Date
CA1102036A true CA1102036A (fr)	1981-05-26

Family

ID=4110647

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CA295,836A Expired CA1102036A (fr)	1978-01-27	1978-01-27	Compose d'enduction a forte teneur en solides

Country Status (1)

Country	Link
CA (1)	CA1102036A (fr)

1978
- 1978-01-27 CA CA295,836A patent/CA1102036A/fr not_active Expired

Legal Events

Date	Code	Title	Description
1998-05-26	MKEX	Expiry

Publication	Publication Date	Title
US4243705A (en)	1981-01-06	Process for coating high solids coating compositions
US4754014A (en)	1988-06-28	Polysiloxane graft copolymers, flexible coating compositions comprising same and branched polysiloxane macromers for preparing same
US4397989A (en)	1983-08-09	High solids coating composition of an acrylic polymer a polyester polyol and an alkylated melamine crosslinking agent
US4673718A (en)	1987-06-16	Polysiloxane graft copolymers, flexible coating compositions comprising same and branched polysiloxane macromers for preparing same
US4766185A (en)	1988-08-23	Polysiloxane graft copolymers, flexible coating compositions comprising same and branched polysiloxane macromers for preparing same - II
US4322508A (en)	1982-03-30	High solids paint composition comprising hydroxy functional oligoesters and hydroxy functional copolymers
US4727100A (en)	1988-02-23	Coating composition containing a reactive urethane component an acrylic fatty acid drying oil resin and a metallic alkylate
US5541268A (en)	1996-07-30	Coating composition
US4873298A (en)	1989-10-10	Polysiloxane graft copolymers, flexible coating compositions comprising same and branched polysiloxane macromers for preparing same II
US4396672A (en)	1983-08-02	Substrate having a pigmented color coat and a clear coat of a _composition of an acrylic, polyester and a melamine resin
US4350790A (en)	1982-09-21	Composition with latent reactive catalyst
CA2135412A1 (fr)	1995-05-13	Agents de revetements multicouches transparents, et utilisation de ces agents dans la realisation de revetements multicouche
US4810759A (en)	1989-03-07	Polyester graft copolymers, flexible coating compositions comprising same and branched polyester macromers for preparing same II
EP1201690B1 (fr)	2004-07-28	Compositions de copolymères de (meth)acrylate hydroxy-fonctionalisés ainsi que des compositions de revêtement
US4276392A (en)	1981-06-30	Coating composition catalyzed with phosphonic acid derivative - #3
US5741880A (en)	1998-04-21	Clearcoating compositions
US4804732A (en)	1989-02-14	Polysiloxane graft copolymers, flexible coating compositions comprising same and branched polysiloxane macromers for preparing same
US5698330A (en)	1997-12-16	Coating compositions for transparent topcoat lacquer layers and the use thereof in processes for the production of multi-layer lacquer coatings
KR100486798B1 (ko)	2005-12-21	내스크래치성코팅조성물
US5157100A (en)	1992-10-20	Method for extending the pot-life of polyol-polyisocyanate mixtures
US4690980A (en)	1987-09-01	Acrylic modified polymers
US4560494A (en)	1985-12-24	Isocyanate functional prepolymers and coating materials based thereon
US4619955A (en)	1986-10-28	Isocyanate functional urethanes as flexibilizing additives in coating vehicles
US4946744A (en)	1990-08-07	Substrate coated with a clearcoat/basecoat composition comprising an anhydride-functional compound and an hydroxy-functional compound
US4952626A (en)	1990-08-28	Polyester graft copolymers, flexible coating compositions comprising same and branched polyester macromonomers for preparing same - II