CA1131845A - Melanges a faible p.m. de polyesters a fonction hydroxy-terminale et produits de revetement derives - Google Patents

Melanges a faible p.m. de polyesters a fonction hydroxy-terminale et produits de revetement derives

Info

Publication number: CA1131845A
Authority: CA; Canada
Prior art keywords: weight; blend; polyester; parts; coating composition
Prior art date: 1976-07-12
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

CA282,417A

Other languages

English (en)

Inventor

Joseph A. Antonelli

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.)

EIDP Inc

Original Assignee

EI Du Pont de Nemours and 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.)

1976-07-12

Filing date

1977-07-11

Publication date

1982-09-14

1977-07-11 Application filed by EI Du Pont de Nemours and Co filed Critical EI Du Pont de Nemours and Co

1982-09-14 Application granted granted Critical

1982-09-14 Publication of CA1131845A publication Critical patent/CA1131845A/fr

Status Expired legal-status Critical Current

Links

239000000203 mixture Substances 0.000 title claims abstract description 95
229920000728 polyester Polymers 0.000 title claims abstract description 77
238000000576 coating method Methods 0.000 title abstract description 21
239000007787 solid Substances 0.000 claims abstract description 19
239000003431 cross linking reagent Substances 0.000 claims abstract description 15
229920005989 resin Polymers 0.000 claims abstract description 10
239000011347 resin Substances 0.000 claims abstract description 10
QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 claims abstract description 8
239000005056 polyisocyanate Substances 0.000 claims abstract description 5
229920001228 polyisocyanate Polymers 0.000 claims abstract description 5
239000008199 coating composition Substances 0.000 claims description 46
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 14
239000000049 pigment Substances 0.000 claims description 9
239000003054 catalyst Substances 0.000 claims description 7
239000003795 chemical substances by application Substances 0.000 claims description 7
239000002270 dispersing agent Substances 0.000 claims description 4
238000000518 rheometry Methods 0.000 claims description 4
235000011037 adipic acid Nutrition 0.000 claims description 2
150000001279 adipic acids Chemical class 0.000 claims description 2
150000002311 glutaric acids Chemical class 0.000 claims description 2
230000001737 promoting effect Effects 0.000 claims description 2
150000003444 succinic acids Chemical class 0.000 claims description 2
QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims 3
150000002148 esters Chemical class 0.000 abstract description 17
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract description 10
125000001931 aliphatic group Chemical group 0.000 abstract description 10
150000002009 diols Chemical class 0.000 abstract description 8
-1 iso-phthalic acid Chemical class 0.000 abstract description 6
229910052757 nitrogen Inorganic materials 0.000 abstract description 5
239000000758 substrate Substances 0.000 abstract description 4
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 abstract description 3
150000004702 methyl esters Chemical class 0.000 abstract description 3
238000010186 staining Methods 0.000 abstract description 3
239000000306 component Substances 0.000 description 20
239000011248 coating agent Substances 0.000 description 13
239000002253 acid Substances 0.000 description 11
JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 11
238000002360 preparation method Methods 0.000 description 10
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 9
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 9
238000000034 method Methods 0.000 description 8
SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 8
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 4
229920000877 Melamine resin Polymers 0.000 description 4
238000006243 chemical reaction Methods 0.000 description 4
239000006185 dispersion Substances 0.000 description 4
238000002156 mixing Methods 0.000 description 4
239000002904 solvent Substances 0.000 description 4
ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
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 3
239000004971 Cross linker Substances 0.000 description 3
OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 3
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
150000008064 anhydrides Chemical class 0.000 description 3
238000005336 cracking Methods 0.000 description 3
IVJISJACKSSFGE-UHFFFAOYSA-N formaldehyde;1,3,5-triazine-2,4,6-triamine Chemical compound O=C.NC1=NC(N)=NC(N)=N1 IVJISJACKSSFGE-UHFFFAOYSA-N 0.000 description 3
239000004615 ingredient Substances 0.000 description 3
229920000642 polymer Polymers 0.000 description 3
239000000047 product Substances 0.000 description 3
239000007921 spray Substances 0.000 description 3
238000012360 testing method Methods 0.000 description 3
UUFQTNFCRMXOAE-UHFFFAOYSA-N 1-methylmethylene Chemical compound C[CH] UUFQTNFCRMXOAE-UHFFFAOYSA-N 0.000 description 2
HGINCPLSRVDWNT-UHFFFAOYSA-N Acrolein Chemical compound C=CC=O HGINCPLSRVDWNT-UHFFFAOYSA-N 0.000 description 2
229920001634 Copolyester Polymers 0.000 description 2
UDSFAEKRVUSQDD-UHFFFAOYSA-N Dimethyl adipate Chemical compound COC(=O)CCCCC(=O)OC UDSFAEKRVUSQDD-UHFFFAOYSA-N 0.000 description 2
MUXOBHXGJLMRAB-UHFFFAOYSA-N Dimethyl succinate Chemical compound COC(=O)CCC(=O)OC MUXOBHXGJLMRAB-UHFFFAOYSA-N 0.000 description 2
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
UKLDJPRMSDWDSL-UHFFFAOYSA-L [dibutyl(dodecanoyloxy)stannyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCCCCCC UKLDJPRMSDWDSL-UHFFFAOYSA-L 0.000 description 2
NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
150000001299 aldehydes Chemical class 0.000 description 2
229920000180 alkyd Polymers 0.000 description 2
229920003180 amino resin Polymers 0.000 description 2
229940072049 amyl acetate Drugs 0.000 description 2
PGMYKACGEOXYJE-UHFFFAOYSA-N anhydrous amyl acetate Natural products CCCCCOC(C)=O PGMYKACGEOXYJE-UHFFFAOYSA-N 0.000 description 2
239000000470 constituent Substances 0.000 description 2
230000032798 delamination Effects 0.000 description 2
239000012975 dibutyltin dilaurate Substances 0.000 description 2
VNGOYPQMJFJDLV-UHFFFAOYSA-N dimethyl benzene-1,3-dicarboxylate Chemical compound COC(=O)C1=CC=CC(C(=O)OC)=C1 VNGOYPQMJFJDLV-UHFFFAOYSA-N 0.000 description 2
XTDYIOOONNVFMA-UHFFFAOYSA-N dimethyl pentanedioate Chemical compound COC(=O)CCCC(=O)OC XTDYIOOONNVFMA-UHFFFAOYSA-N 0.000 description 2
239000003822 epoxy resin Substances 0.000 description 2
239000012467 final product Substances 0.000 description 2
MNWFXJYAOYHMED-UHFFFAOYSA-M heptanoate Chemical compound CCCCCCC([O-])=O MNWFXJYAOYHMED-UHFFFAOYSA-M 0.000 description 2
239000007788 liquid Substances 0.000 description 2
150000003022 phthalic acids Chemical class 0.000 description 2
229920000647 polyepoxide Polymers 0.000 description 2
239000000126 substance Substances 0.000 description 2
229920001187 thermosetting polymer Polymers 0.000 description 2
238000005406 washing Methods 0.000 description 2
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
NGZXDRGWBULKFA-NSOVKSMOSA-N (+)-Bebeerine Chemical compound C([C@@H]1N(C)CCC=2C=C(C(=C(OC3=CC=C(C=C3)C[C@H]3C=4C=C(C(=CC=4CCN3C)OC)O3)C=21)O)OC)C1=CC=C(O)C3=C1 NGZXDRGWBULKFA-NSOVKSMOSA-N 0.000 description 1
KGRVJHAUYBGFFP-UHFFFAOYSA-N 2,2'-Methylenebis(4-methyl-6-tert-butylphenol) Chemical compound CC(C)(C)C1=CC(C)=CC(CC=2C(=C(C=C(C)C=2)C(C)(C)C)O)=C1O KGRVJHAUYBGFFP-UHFFFAOYSA-N 0.000 description 1
SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
GOXQRTZXKQZDDN-UHFFFAOYSA-N 2-Ethylhexyl acrylate Chemical compound CCCCC(CC)COC(=O)C=C GOXQRTZXKQZDDN-UHFFFAOYSA-N 0.000 description 1
SVONRAPFKPVNKG-UHFFFAOYSA-N 2-ethoxyethyl acetate Chemical compound CCOCCOC(C)=O SVONRAPFKPVNKG-UHFFFAOYSA-N 0.000 description 1
OMIGHNLMNHATMP-UHFFFAOYSA-N 2-hydroxyethyl prop-2-enoate Chemical compound OCCOC(=O)C=C OMIGHNLMNHATMP-UHFFFAOYSA-N 0.000 description 1
241000219198 Brassica Species 0.000 description 1
235000003351 Brassica cretica Nutrition 0.000 description 1
235000003343 Brassica rupestris Nutrition 0.000 description 1
101100167062 Caenorhabditis elegans chch-3 gene Proteins 0.000 description 1
239000004805 Cyclohexane-1,2-dicarboxylic acid Substances 0.000 description 1
239000005058 Isophorone diisocyanate Substances 0.000 description 1
VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical class COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 1
229920001730 Moisture cure polyurethane Polymers 0.000 description 1
241000282337 Nasua nasua Species 0.000 description 1
229930040373 Paraformaldehyde Natural products 0.000 description 1
229910000831 Steel Inorganic materials 0.000 description 1
GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
229920001807 Urea-formaldehyde Polymers 0.000 description 1
IKHGUXGNUITLKF-XPULMUKRSA-N acetaldehyde Chemical compound [14CH]([14CH3])=O IKHGUXGNUITLKF-XPULMUKRSA-N 0.000 description 1
239000003377 acid catalyst Substances 0.000 description 1
230000002378 acidificating effect Effects 0.000 description 1
150000007513 acids Chemical class 0.000 description 1
239000000654 additive Substances 0.000 description 1
WNLRTRBMVRJNCN-UHFFFAOYSA-L adipate(2-) Chemical compound [O-]C(=O)CCCCC([O-])=O WNLRTRBMVRJNCN-UHFFFAOYSA-L 0.000 description 1
239000002671 adjuvant Substances 0.000 description 1
150000007933 aliphatic carboxylic acids Chemical class 0.000 description 1
150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
229910052782 aluminium Inorganic materials 0.000 description 1
125000003118 aryl group Chemical group 0.000 description 1
238000000889 atomisation Methods 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
QKSKPIVNLNLAAV-UHFFFAOYSA-N bis(2-chloroethyl) sulfide Chemical compound ClCCSCCCl QKSKPIVNLNLAAV-UHFFFAOYSA-N 0.000 description 1
OHJMTUPIZMNBFR-UHFFFAOYSA-N biuret Chemical compound NC(=O)NC(N)=O OHJMTUPIZMNBFR-UHFFFAOYSA-N 0.000 description 1
CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 1
239000004202 carbamide Substances 0.000 description 1
125000004432 carbon atom Chemical group C* 0.000 description 1
239000010960 cold rolled steel Substances 0.000 description 1
239000003086 colorant Substances 0.000 description 1
230000000295 complement effect Effects 0.000 description 1
238000009833 condensation Methods 0.000 description 1
230000005494 condensation Effects 0.000 description 1
238000007796 conventional method Methods 0.000 description 1
238000004132 cross linking Methods 0.000 description 1
MLUCVPSAIODCQM-NSCUHMNNSA-N crotonaldehyde Chemical compound C\C=C\C=O MLUCVPSAIODCQM-NSCUHMNNSA-N 0.000 description 1
MLUCVPSAIODCQM-UHFFFAOYSA-N crotonaldehyde Natural products CC=CC=O MLUCVPSAIODCQM-UHFFFAOYSA-N 0.000 description 1
239000013078 crystal Substances 0.000 description 1
125000004122 cyclic group Chemical group 0.000 description 1
QSAWQNUELGIYBC-UHFFFAOYSA-N cyclohexane-1,2-dicarboxylic acid Chemical compound OC(=O)C1CCCCC1C(O)=O QSAWQNUELGIYBC-UHFFFAOYSA-N 0.000 description 1
230000007423 decrease Effects 0.000 description 1
150000001991 dicarboxylic acids Chemical class 0.000 description 1
QGBSISYHAICWAH-UHFFFAOYSA-N dicyandiamide Chemical compound NC(N)=NC#N QGBSISYHAICWAH-UHFFFAOYSA-N 0.000 description 1
125000005442 diisocyanate group Chemical group 0.000 description 1
239000003085 diluting agent Substances 0.000 description 1
230000000694 effects Effects 0.000 description 1
239000012530 fluid Substances 0.000 description 1
238000005227 gel permeation chromatography Methods 0.000 description 1
JFCQEDHGNNZCLN-UHFFFAOYSA-N glutaric acid Chemical compound OC(=O)CCCC(O)=O JFCQEDHGNNZCLN-UHFFFAOYSA-N 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
238000007542 hardness measurement Methods 0.000 description 1
125000004836 hexamethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[*:1] 0.000 description 1
ANJPRQPHZGHVQB-UHFFFAOYSA-N hexyl isocyanate Chemical compound CCCCCCN=C=O ANJPRQPHZGHVQB-UHFFFAOYSA-N 0.000 description 1
YAMHXTCMCPHKLN-UHFFFAOYSA-N imidazolidin-2-one Chemical compound O=C1NCCN1 YAMHXTCMCPHKLN-UHFFFAOYSA-N 0.000 description 1
239000006115 industrial coating Substances 0.000 description 1
150000002500 ions Chemical class 0.000 description 1
229910000398 iron phosphate Inorganic materials 0.000 description 1
WBJZTOZJJYAKHQ-UHFFFAOYSA-K iron(3+) phosphate Chemical compound [Fe+3].[O-]P([O-])([O-])=O WBJZTOZJJYAKHQ-UHFFFAOYSA-K 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
239000000463 material Substances 0.000 description 1
238000005259 measurement Methods 0.000 description 1
150000007974 melamines Chemical class 0.000 description 1
WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 1
238000003801 milling Methods 0.000 description 1
239000003607 modifier Substances 0.000 description 1
125000000896 monocarboxylic acid group Chemical group 0.000 description 1
235000010460 mustard Nutrition 0.000 description 1
KYTZHLUVELPASH-UHFFFAOYSA-N naphthalene-1,2-dicarboxylic acid Chemical compound C1=CC=CC2=C(C(O)=O)C(C(=O)O)=CC=C21 KYTZHLUVELPASH-UHFFFAOYSA-N 0.000 description 1
125000001971 neopentyl group Chemical group [H]C([*])([H])C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
239000001048 orange dye Substances 0.000 description 1
238000007746 phosphate conversion coating Methods 0.000 description 1
229920000058 polyacrylate Polymers 0.000 description 1
229920001451 polypropylene glycol Polymers 0.000 description 1
239000000376 reactant Substances 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
239000004576 sand Substances 0.000 description 1
239000000344 soap Substances 0.000 description 1
238000005507 spraying Methods 0.000 description 1
239000003381 stabilizer Substances 0.000 description 1
239000010959 steel Substances 0.000 description 1
CMQCNTNASCDNGR-UHFFFAOYSA-N toluene;hydrate Chemical compound O.CC1=CC=CC=C1 CMQCNTNASCDNGR-UHFFFAOYSA-N 0.000 description 1
QQOWHRYOXYEMTL-UHFFFAOYSA-N triazin-4-amine Chemical class N=C1C=CN=NN1 QQOWHRYOXYEMTL-UHFFFAOYSA-N 0.000 description 1
150000003628 tricarboxylic acids Chemical class 0.000 description 1
239000002699 waste material Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L67/00—Compositions of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Compositions of derivatives of such polymers
- C08L67/02—Polyesters derived from dicarboxylic acids and dihydroxy compounds
- 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
- C08G18/42—Polycondensates having carboxylic or carbonic ester groups in the main chain
- C08G18/4202—Two or more polyesters of different physical or chemical nature
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L67/00—Compositions of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Compositions of derivatives of such polymers
- C08L67/06—Unsaturated polyesters

Landscapes

Chemical & Material Sciences (AREA)
Health & Medical Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Organic Chemistry (AREA)
Paints Or Removers (AREA)
Polyesters Or Polycarbonates (AREA)
Polyurethanes Or Polyureas (AREA)
Compositions Of Macromolecular Compounds (AREA)

CA282,417A 1976-07-12 1977-07-11 Melanges a faible p.m. de polyesters a fonction hydroxy-terminale et produits de revetement derives Expired CA1131845A (fr)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
US70436676A	1976-07-12	1976-07-12
US704,366		1985-02-22

Publications (1)

Publication Number	Publication Date
CA1131845A true CA1131845A (fr)	1982-09-14

Family

ID=24829171

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CA282,417A Expired CA1131845A (fr)	1976-07-12	1977-07-11	Melanges a faible p.m. de polyesters a fonction hydroxy-terminale et produits de revetement derives

Country Status (9)

Country	Link
JP (1)	JPS538653A (fr)
AT (1)	AT357245B (fr)
AU (1)	AU519914B2 (fr)
CA (1)	CA1131845A (fr)
DE (1)	DE2731488A1 (fr)
FR (1)	FR2358442A1 (fr)
GB (1)	GB1561076A (fr)
NL (1)	NL186772C (fr)
ZA (1)	ZA774147B (fr)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4369283A (en)	1981-03-06	1983-01-18	E. I. Du Pont De Nemours & Company	High solids can coating composition containing epoxy, acrylic and aminoplast resins
DE4039220A1 (de) *	1990-12-08	1992-06-11	Basf Lacke & Farben	Beschichtungsmittel mit hohem feststoffgehalt
JP5483670B2 (ja) *	2008-12-26	2014-05-07	竹本油脂株式会社	非水系顔料分散剤及び顔料組成物

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3296211A (en) *	1961-11-01	1967-01-03	Aerojet General Co	Hydroxy-terminated polyesters
ES382338A1 (es) *	1969-12-15	1972-11-16	Koppers Co Inc	Un procedimiento para preparar una resina de poliester.
DE2146754C3 (de) *	1971-09-18	1982-05-27	Chemische Werke Hüls AG, 4370 Marl	Überzugsmittel
AU466953B2 (en) *	1972-05-24	1975-11-13	Dulux Australia Limited	Thermosetting coating compositions
US3893959A (en) *	1973-10-24	1975-07-08	American Cyanamid Co	Alkyl resin containing an oligomer mixture of unsaturated long chain fatty acids

1977
- 1977-07-08 AU AU26882/77A patent/AU519914B2/en not_active Expired
- 1977-07-11 AT AT495977A patent/AT357245B/de not_active IP Right Cessation
- 1977-07-11 GB GB29002/77A patent/GB1561076A/en not_active Expired
- 1977-07-11 FR FR7721330A patent/FR2358442A1/fr active Granted
- 1977-07-11 ZA ZA00774147A patent/ZA774147B/xx unknown
- 1977-07-11 CA CA282,417A patent/CA1131845A/fr not_active Expired
- 1977-07-12 JP JP8350077A patent/JPS538653A/ja active Granted
- 1977-07-12 DE DE19772731488 patent/DE2731488A1/de active Granted
- 1977-07-12 NL NLAANVRAGE7707759,A patent/NL186772C/xx not_active IP Right Cessation

Also Published As

Publication number	Publication date
NL186772C (nl)	1991-02-18
DE2731488C2 (fr)	1989-03-02
GB1561076A (en)	1980-02-13
NL7707759A (nl)	1978-01-16
JPS6138218B2 (fr)	1986-08-28
AU519914B2 (en)	1982-01-07
FR2358442A1 (fr)	1978-02-10
FR2358442B1 (fr)	1984-05-11
AT357245B (de)	1980-06-25
JPS538653A (en)	1978-01-26
ATA495977A (de)	1979-11-15
DE2731488A1 (de)	1978-01-19
ZA774147B (en)	1978-05-30
AU2688277A (en)	1979-01-11
NL186772B (nl)	1990-09-17

Legal Events

Date	Code	Title	Description
1999-09-14	MKEX	Expiry

Publication	Publication Date	Title
US6646049B2 (en)	2003-11-11	High-solids thermoset binders formed using hyperbranched polyols as reactive intermediates, coating compositions formed therewith, and methods of making and using same
US4317894A (en)	1982-03-02	Low temperature cure coating compositions
EP0391166B1 (fr)	1993-11-03	Revêtements résistant à l'écaillement et procédés d'application
US4339365A (en)	1982-07-13	Coating compositions containing pigment dispersants
US4338379A (en)	1982-07-06	High-solids thermosetting enamel coating composition
EP0896991B1 (fr)	2003-04-02	Polymères d'acrylates à base de polyesters ou d' oligomères de polyesters, leur préparation et leur utilisation dans des peintures
US4192826A (en)	1980-03-11	Thermosetting, electrostatically sprayable compositions containing blocked acid catalyst
US4916188A (en)	1990-04-10	Fluorocarbon powder paints
DE69803795T2 (de)	2002-08-08	Zusammensetzungen mit hohem feststoffgehalt
DE60309499T2 (de)	2007-05-31	Polyesterzusammensetzung für metallbandbeschichtung (coil coating), verfahren zur metallbandbeschichtung und beschichtetes metallband
CA2464241C (fr)	2008-11-04	Compositions et methode pour l'enduction en continu de bandes a amorcage automatique
NL9002380A (nl)	1992-06-01	Bindmiddelsamenstelling op basis van een acrylaatpolymeer en een kruisvernetter op basis van een acetoacetaatverbinding.
EP0843706A1 (fr)	1998-05-27	Laquage multicouche, son procede de realisation et laque de finition non aqueuse appropriee a cet effet
EP0324334B1 (fr)	1991-10-09	Liants diluables dans l'eau, un procédé pour leur préparation et leur utilisation
WO1995012640A1 (fr)	1995-05-11	Compositions de revetement thermodurcissables
US3261881A (en)	1966-07-19	Coating composition of a carboxylic acid amide polymer and an organopolysiloxane resin
EP0719307A1 (fr)	1996-07-03	Peintures non aqueuses
US4619955A (en)	1986-10-28	Isocyanate functional urethanes as flexibilizing additives in coating vehicles
CA1337887C (fr)	1996-01-02	Revetements reactifs
US4254235A (en)	1981-03-03	Thermosetting powder paints
CA1131845A (fr)	1982-09-14	Melanges a faible p.m. de polyesters a fonction hydroxy-terminale et produits de revetement derives
US4424296A (en)	1984-01-03	Blends of low molecular weight hydroxy-terminated polyesters and coatings based on these blends
DE2539104C3 (de)	1986-07-10	Lösungsmittelarme Einbrennlacke
CA2103368A1 (fr)	1992-12-11	Compositions de revetement thermodurcissables
CA2238777C (fr)	2002-04-23	Polyesters a fonction hydroxy, de faible masse molaire, pour revetements