NO331887B1 - Alkydharpiksemulsjon for dekklakker, samt fremgangsmate for fremstilling og anvendelser derav - Google Patents

Alkydharpiksemulsjon for dekklakker, samt fremgangsmate for fremstilling og anvendelser derav Download PDF

Info

Publication number: NO331887B1
Authority: NO; Norway
Prior art keywords: alkyd resin; mol; mass; water; alkyd
Prior art date: 2003-04-21

Application number

NO20055469A

Other languages

English (en)

Norwegian (no)

Other versions

NO20055469L (no

NO20055469D0 (no

Inventor

Edmund Urbano

Michael Gobec

Oliver Ferk

Original Assignee

Cytec Surface Specialties At

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.)

2003-04-21

Filing date

2005-11-18

Publication date

2012-04-30

2005-11-18 Application filed by Cytec Surface Specialties At filed Critical Cytec Surface Specialties At

2005-11-18 Publication of NO20055469D0 publication Critical patent/NO20055469D0/no

2006-01-10 Publication of NO20055469L publication Critical patent/NO20055469L/no

2012-04-30 Publication of NO331887B1 publication Critical patent/NO331887B1/no

Links

229920000180 alkyd Polymers 0.000 claims abstract description 92
239000000839 emulsion Substances 0.000 claims abstract description 46
229920005989 resin Polymers 0.000 claims abstract description 37
239000011347 resin Substances 0.000 claims abstract description 37
239000000463 material Substances 0.000 claims abstract description 11
230000001804 emulsifying effect Effects 0.000 claims abstract description 10
230000032050 esterification Effects 0.000 claims abstract description 9
238000005886 esterification reaction Methods 0.000 claims abstract description 9
OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims abstract description 8
239000011248 coating agent Substances 0.000 claims abstract description 8
238000004519 manufacturing process Methods 0.000 claims abstract description 8
238000000576 coating method Methods 0.000 claims abstract description 7
229910052751 metal Inorganic materials 0.000 claims abstract description 5
239000002184 metal Substances 0.000 claims abstract description 5
229910052500 inorganic mineral Inorganic materials 0.000 claims abstract description 4
239000011707 mineral Substances 0.000 claims abstract description 4
239000004753 textile Substances 0.000 claims abstract description 4
239000002023 wood Substances 0.000 claims abstract description 4
239000000758 substrate Substances 0.000 claims abstract description 3
150000002739 metals Chemical class 0.000 claims abstract 2
239000000203 mixture Substances 0.000 claims description 24
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 22
239000007787 solid Substances 0.000 claims description 21
239000002253 acid Substances 0.000 claims description 15
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 12
239000002966 varnish Substances 0.000 claims description 12
238000000034 method Methods 0.000 claims description 11
239000011230 binding agent Substances 0.000 claims description 10
239000003921 oil Substances 0.000 claims description 8
239000003054 catalyst Substances 0.000 claims description 6
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims description 6
239000011541 reaction mixture Substances 0.000 claims description 6
150000008065 acid anhydrides Chemical class 0.000 claims description 3
239000000376 reactant Substances 0.000 claims 1
229920001223 polyethylene glycol Polymers 0.000 abstract description 12
239000002202 Polyethylene glycol Substances 0.000 abstract description 10
125000000229 (C1-C4)alkoxy group Chemical group 0.000 abstract 1
239000003995 emulsifying agent Substances 0.000 description 15
239000000243 solution Substances 0.000 description 12
239000003795 chemical substances by application Substances 0.000 description 9
235000019198 oils Nutrition 0.000 description 8
238000003860 storage Methods 0.000 description 8
239000000126 substance Substances 0.000 description 7
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 6
125000000217 alkyl group Chemical group 0.000 description 6
238000001035 drying Methods 0.000 description 6
239000000049 pigment Substances 0.000 description 6
235000014113 dietary fatty acids Nutrition 0.000 description 5
239000006185 dispersion Substances 0.000 description 5
239000000194 fatty acid Substances 0.000 description 5
229930195729 fatty acid Natural products 0.000 description 5
150000004665 fatty acids Chemical class 0.000 description 5
239000002904 solvent Substances 0.000 description 5
RSWGJHLUYNHPMX-UHFFFAOYSA-N 1,4a-dimethyl-7-propan-2-yl-2,3,4,4b,5,6,10,10a-octahydrophenanthrene-1-carboxylic acid Chemical compound C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 4
LAIUFBWHERIJIH-UHFFFAOYSA-N 3-Methylheptane Chemical compound CCCCC(C)CC LAIUFBWHERIJIH-UHFFFAOYSA-N 0.000 description 4
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 4
239000000654 additive Substances 0.000 description 4
125000003545 alkoxy group Chemical group 0.000 description 4
239000007864 aqueous solution Substances 0.000 description 4
-1 benzoic acid Chemical class 0.000 description 4
238000006243 chemical reaction Methods 0.000 description 4
238000000265 homogenisation Methods 0.000 description 4
125000002887 hydroxy group Chemical group [H]O* 0.000 description 4
239000008096 xylene Substances 0.000 description 4
238000004383 yellowing Methods 0.000 description 4
ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 3
WMFOQBRAJBCJND-UHFFFAOYSA-M Lithium hydroxide Chemical compound [Li+].[OH-] WMFOQBRAJBCJND-UHFFFAOYSA-M 0.000 description 3
LGRFSURHDFAFJT-UHFFFAOYSA-N Phthalic anhydride Natural products C1=CC=C2C(=O)OC(=O)C2=C1 LGRFSURHDFAFJT-UHFFFAOYSA-N 0.000 description 3
DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 3
GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 3
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
230000002378 acidificating effect Effects 0.000 description 3
230000000996 additive effect Effects 0.000 description 3
238000010533 azeotropic distillation Methods 0.000 description 3
230000015572 biosynthetic process Effects 0.000 description 3
JHIWVOJDXOSYLW-UHFFFAOYSA-N butyl 2,2-difluorocyclopropane-1-carboxylate Chemical compound CCCCOC(=O)C1CC1(F)F JHIWVOJDXOSYLW-UHFFFAOYSA-N 0.000 description 3
150000001735 carboxylic acids Chemical class 0.000 description 3
238000004821 distillation Methods 0.000 description 3
238000004945 emulsification Methods 0.000 description 3
239000011630 iodine Substances 0.000 description 3
229910052740 iodine Inorganic materials 0.000 description 3
239000004922 lacquer Substances 0.000 description 3
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 3
238000002156 mixing Methods 0.000 description 3
238000006386 neutralization reaction Methods 0.000 description 3
229920003023 plastic Polymers 0.000 description 3
239000004033 plastic Substances 0.000 description 3
229920002635 polyurethane Polymers 0.000 description 3
239000004814 polyurethane Substances 0.000 description 3
KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 3
KMOUUZVZFBCRAM-OLQVQODUSA-N (3as,7ar)-3a,4,7,7a-tetrahydro-2-benzofuran-1,3-dione Chemical compound C1C=CC[C@@H]2C(=O)OC(=O)[C@@H]21 KMOUUZVZFBCRAM-OLQVQODUSA-N 0.000 description 2
QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
150000007513 acids Chemical class 0.000 description 2
229910001854 alkali hydroxide Inorganic materials 0.000 description 2
WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 2
125000004432 carbon atom Chemical group C* 0.000 description 2
239000004359 castor oil Substances 0.000 description 2
235000019438 castor oil Nutrition 0.000 description 2
230000018044 dehydration Effects 0.000 description 2
238000006297 dehydration reaction Methods 0.000 description 2
239000008367 deionised water Substances 0.000 description 2
229910021641 deionized water Inorganic materials 0.000 description 2
150000001991 dicarboxylic acids Chemical class 0.000 description 2
239000002270 dispersing agent Substances 0.000 description 2
238000004090 dissolution Methods 0.000 description 2
239000003925 fat Substances 0.000 description 2
150000002191 fatty alcohols Chemical class 0.000 description 2
238000009472 formulation Methods 0.000 description 2
ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 2
ZUBZATZOEPUUQF-UHFFFAOYSA-N isononane Chemical compound CCCCCCC(C)C ZUBZATZOEPUUQF-UHFFFAOYSA-N 0.000 description 2
150000002762 monocarboxylic acid derivatives Chemical class 0.000 description 2
BDERNNFJNOPAEC-UHFFFAOYSA-N n-propyl alcohol Natural products CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 2
230000003472 neutralizing effect Effects 0.000 description 2
230000001590 oxidative effect Effects 0.000 description 2
239000003973 paint Substances 0.000 description 2
229920000058 polyacrylate Polymers 0.000 description 2
238000002360 preparation method Methods 0.000 description 2
238000000518 rheometry Methods 0.000 description 2
238000007127 saponification reaction Methods 0.000 description 2
230000006641 stabilisation Effects 0.000 description 2
238000011105 stabilization Methods 0.000 description 2
150000005846 sugar alcohols Chemical class 0.000 description 2
239000003784 tall oil Substances 0.000 description 2
239000002562 thickening agent Substances 0.000 description 2
229910052726 zirconium Inorganic materials 0.000 description 2
JNYAEWCLZODPBN-JGWLITMVSA-N (2r,3r,4s)-2-[(1r)-1,2-dihydroxyethyl]oxolane-3,4-diol Chemical class OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O JNYAEWCLZODPBN-JGWLITMVSA-N 0.000 description 1
MUTGBJKUEZFXGO-OLQVQODUSA-N (3as,7ar)-3a,4,5,6,7,7a-hexahydro-2-benzofuran-1,3-dione Chemical compound C1CCC[C@@H]2C(=O)OC(=O)[C@@H]21 MUTGBJKUEZFXGO-OLQVQODUSA-N 0.000 description 1
FALRKNHUBBKYCC-UHFFFAOYSA-N 2-(chloromethyl)pyridine-3-carbonitrile Chemical compound ClCC1=NC=CC=C1C#N FALRKNHUBBKYCC-UHFFFAOYSA-N 0.000 description 1
WZFUQSJFWNHZHM-UHFFFAOYSA-N 2-[4-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]piperazin-1-yl]-1-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)ethanone Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)N1CCN(CC1)CC(=O)N1CC2=C(CC1)NN=N2 WZFUQSJFWNHZHM-UHFFFAOYSA-N 0.000 description 1
ZDFKSZDMHJHQHS-UHFFFAOYSA-N 2-tert-butylbenzoic acid Chemical class CC(C)(C)C1=CC=CC=C1C(O)=O ZDFKSZDMHJHQHS-UHFFFAOYSA-N 0.000 description 1
MWSKJDNQKGCKPA-UHFFFAOYSA-N 6-methyl-3a,4,5,7a-tetrahydro-2-benzofuran-1,3-dione Chemical compound C1CC(C)=CC2C(=O)OC(=O)C12 MWSKJDNQKGCKPA-UHFFFAOYSA-N 0.000 description 1
OAOABCKPVCUNKO-UHFFFAOYSA-N 8-methyl Nonanoic acid Chemical compound CC(C)CCCCCCC(O)=O OAOABCKPVCUNKO-UHFFFAOYSA-N 0.000 description 1
239000004925 Acrylic resin Substances 0.000 description 1
229920000178 Acrylic resin Polymers 0.000 description 1
241000251468 Actinopterygii Species 0.000 description 1
239000005711 Benzoic acid Substances 0.000 description 1
244000020518 Carthamus tinctorius Species 0.000 description 1
244000068988 Glycine max Species 0.000 description 1
235000010469 Glycine max Nutrition 0.000 description 1
244000020551 Helianthus annuus Species 0.000 description 1
235000003222 Helianthus annuus Nutrition 0.000 description 1
240000006240 Linum usitatissimum Species 0.000 description 1
235000004431 Linum usitatissimum Nutrition 0.000 description 1
LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 1
229910000831 Steel Inorganic materials 0.000 description 1
DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 description 1
QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 description 1
UKLDJPRMSDWDSL-UHFFFAOYSA-L [dibutyl(dodecanoyloxy)stannyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCCCCCC UKLDJPRMSDWDSL-UHFFFAOYSA-L 0.000 description 1
230000002411 adverse Effects 0.000 description 1
238000007605 air drying Methods 0.000 description 1
150000001299 aldehydes Chemical class 0.000 description 1
239000003513 alkali Substances 0.000 description 1
150000008044 alkali metal hydroxides Chemical class 0.000 description 1
229910001860 alkaline earth metal hydroxide Inorganic materials 0.000 description 1
150000001346 alkyl aryl ethers Chemical class 0.000 description 1
150000001412 amines Chemical class 0.000 description 1
229910021529 ammonia Inorganic materials 0.000 description 1
239000002585 base Substances 0.000 description 1
125000005605 benzo group Chemical group 0.000 description 1
235000010233 benzoic acid Nutrition 0.000 description 1
BTANRVKWQNVYAZ-UHFFFAOYSA-N butan-2-ol Chemical compound CCC(C)O BTANRVKWQNVYAZ-UHFFFAOYSA-N 0.000 description 1
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
230000003197 catalytic effect Effects 0.000 description 1
GNEMDYVJKXMKCS-UHFFFAOYSA-N cobalt zirconium Chemical compound [Co].[Zr] GNEMDYVJKXMKCS-UHFFFAOYSA-N 0.000 description 1
230000000052 comparative effect Effects 0.000 description 1
238000001816 cooling Methods 0.000 description 1
239000002385 cottonseed oil Substances 0.000 description 1
235000012343 cottonseed oil Nutrition 0.000 description 1
238000004042 decolorization Methods 0.000 description 1
230000007547 defect Effects 0.000 description 1
230000007812 deficiency Effects 0.000 description 1
239000013530 defoamer Substances 0.000 description 1
239000012975 dibutyltin dilaurate Substances 0.000 description 1
238000010790 dilution Methods 0.000 description 1
239000012895 dilution Substances 0.000 description 1
238000006266 etherification reaction Methods 0.000 description 1
239000010685 fatty oil Substances 0.000 description 1
238000011049 filling Methods 0.000 description 1
235000004426 flaxseed Nutrition 0.000 description 1
239000003517 fume Substances 0.000 description 1
229920000831 ionic polymer Polymers 0.000 description 1
229910052742 iron Inorganic materials 0.000 description 1
ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 description 1
238000006317 isomerization reaction Methods 0.000 description 1
239000000944 linseed oil Substances 0.000 description 1
239000007788 liquid Substances 0.000 description 1
230000014759 maintenance of location Effects 0.000 description 1
FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
238000005259 measurement Methods 0.000 description 1
239000000155 melt Substances 0.000 description 1
239000002480 mineral oil Substances 0.000 description 1
235000010446 mineral oil Nutrition 0.000 description 1
150000002763 monocarboxylic acids Chemical class 0.000 description 1
239000007764 o/w emulsion Substances 0.000 description 1
239000012766 organic filler Substances 0.000 description 1
239000012860 organic pigment Substances 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
229920001568 phenolic resin Polymers 0.000 description 1
239000005011 phenolic resin Substances 0.000 description 1
229920001225 polyester resin Polymers 0.000 description 1
239000004645 polyester resin Substances 0.000 description 1
238000006798 ring closing metathesis reaction Methods 0.000 description 1
239000003813 safflower oil Substances 0.000 description 1
229920006395 saturated elastomer Polymers 0.000 description 1
150000004671 saturated fatty acids Chemical class 0.000 description 1
235000003441 saturated fatty acids Nutrition 0.000 description 1
239000010959 steel Substances 0.000 description 1
238000003756 stirring Methods 0.000 description 1
229940014800 succinic anhydride Drugs 0.000 description 1
239000002600 sunflower oil Substances 0.000 description 1
150000003512 tertiary amines Chemical class 0.000 description 1
239000004408 titanium dioxide Substances 0.000 description 1
150000004670 unsaturated fatty acids Chemical class 0.000 description 1
235000021122 unsaturated fatty acids Nutrition 0.000 description 1
JOYRKODLDBILNP-UHFFFAOYSA-N urethane group Chemical group NC(=O)OCC JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
235000013311 vegetables Nutrition 0.000 description 1
239000003171 wood protecting agent Substances 0.000 description 1

Classifications

- 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
- C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
- C08G63/02—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds
- C08G63/12—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds derived from polycarboxylic acids and polyhydroxy compounds
- C08G63/46—Polyesters chemically modified by esterification
- C08G63/48—Polyesters chemically modified by esterification by unsaturated higher fatty oils or their acids; by resin acids
- 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
- C09D167/08—Polyesters modified with higher fatty oils or their acids, or with natural resins or resin acids
- 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
- C08L67/08—Polyesters modified with higher fatty oils or their acids, or with resins or resin acids

Landscapes

Chemical & Material Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Oil, Petroleum & Natural Gas (AREA)
Organic Chemistry (AREA)
Polymers & Plastics (AREA)
Medicinal Chemistry (AREA)
Health & Medical Sciences (AREA)
General Chemical & Material Sciences (AREA)
Life Sciences & Earth Sciences (AREA)
Engineering & Computer Science (AREA)
Materials Engineering (AREA)
Wood Science & Technology (AREA)
Paints Or Removers (AREA)
Polyesters Or Polycarbonates (AREA)
Compositions Of Macromolecular Compounds (AREA)

NO20055469A 2003-04-21 2005-11-18 Alkydharpiksemulsjon for dekklakker, samt fremgangsmate for fremstilling og anvendelser derav NO331887B1 (no)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
EP03009114A EP1471123A1 (fr)	2003-04-21	2003-04-21	Emulsion à base de résine alkyde pour laque de finition
PCT/EP2004/004115 WO2004094546A1 (fr)	2003-04-21	2004-04-19	Emulsions de resines alkydes pour des vernis de finition

Publications (3)

Publication Number	Publication Date
NO20055469D0 NO20055469D0 (no)	2005-11-18
NO20055469L NO20055469L (no)	2006-01-10
NO331887B1 true NO331887B1 (no)	2012-04-30

Family

ID=32946854

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO20055469A NO331887B1 (no)	2003-04-21	2005-11-18	Alkydharpiksemulsjon for dekklakker, samt fremgangsmate for fremstilling og anvendelser derav

Country Status (8)

Country	Link
US (1)	US7479518B2 (fr)
EP (2)	EP1471123A1 (fr)
AT (1)	ATE514762T1 (fr)
CA (1)	CA2522801C (fr)
ES (1)	ES2368220T3 (fr)
NO (1)	NO331887B1 (fr)
PL (1)	PL1622986T3 (fr)
WO (1)	WO2004094546A1 (fr)

Families Citing this family (11)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
FI20065150L (fi) *	2006-03-06	2007-09-07	Valtion Teknillinen	Modifioitu luonnonrasvahappopohjainen hybridihartsi ja menetelmä sen valmistamiseksi
EP2110410A1 (fr)	2008-04-16	2009-10-21	Cytec Surface Specialties Austria GmbH	Pâte de résine pour pâte de pigment universel
EP2175000A1 (fr) *	2008-10-09	2010-04-14	Cytec Surface Specialties S.A./N.V.	Compositions de Résines Alkydiques Dispersées dans de l'Eau et Réticulables par Rayonnement
CN102317071B (zh)	2008-12-19	2016-02-03	威士伯采购公司	低渗透性、低甲醛的醇酸树脂组合物
EP2365036A1 (fr)	2010-03-12	2011-09-14	Cytec Surface Specialties, S.A.	Compositions de revêtement aqueux durcissable par rayonnement
FR2965267B1 (fr)	2010-09-27	2013-11-15	Cray Valley Sa	Resines polyesters a base d'acides gras de longueur en huile courte, dispersions aqueuses et revetements lies
EP2444436A1 (fr)	2010-10-20	2012-04-25	Cytec Austria GmbH	Composés de résine alkyde modifiés diluable à l'eau
CN102153737B (zh) *	2010-12-27	2013-01-23	嘉宝莉化工集团股份有限公司	聚氨酯固化剂用的高羟基醇酸树脂及其制备方法
EP2964685B1 (fr)	2013-03-06	2020-07-22	Ege Kimya Sanayi ve Ticaret A.S.	Polymères uréthanisés à base de cobalt et de manganèse pour revêtements, peintures et encres à base de polymère séchant à l'air
EP3374455B1 (fr)	2015-11-13	2020-05-06	Ege Kimya Sanayi ve Ticaret A.S.	Polymère uréthanisé avec métal soluble dans un solvant à faible taux de composés organiques volatils
EP3272823A1 (fr)	2016-07-19	2018-01-24	ALLNEX AUSTRIA GmbH	Compositions de siccatifs pour résines alkydes

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3269967A (en)	1960-05-27	1966-08-30	Standard Oil Co	Water emulsion alkyd resin composition comprising water soluble alkanolamine and polyethenoxy ether of alkylphenol
FR1478892A (fr)	1965-05-06	1967-07-17
US3457206A (en)	1966-05-16	1969-07-22	Staley Mfg Co A E	Water dispersible alkyd resins comprising esterified units of an alkoxypolyoxyethylene glycol
AT325742B (de)	1973-11-08	1975-11-10	Vianova Kunstharz Ag	Verfahren zur herstellung von wässerigen dispersionen von alkydharzen
AT333035B (de)	1974-12-23	1976-10-25	Vianova Kunstharz Ag	Verfahren zur herstellung wasseriger dispersionen von alkydharzen
DE2718186A1 (de)	1977-04-23	1978-11-02	Oldorid Kunstoffe Gmbh	Bewetterungslutte fuer den berg- und tunnelbau
BE1007442A3 (nl) *	1993-02-09	1995-07-04	Dsm Nv	Wateroplosbare hars.
DE4306946A1 (de)	1993-03-05	1994-09-08	Hoechst Ag	Ungesättigte Polyurethane und deren Verwendung als Dispergiermittel für Alkydharze
AT409133B (de) *	1998-08-27	2002-05-27	Solutia Austria Gmbh	Strahlenhärtbare wasserlösliche polyesterharz-zusammensetzungen mit hohem feststoffanteil
AT407989B (de)	1999-10-15	2001-07-25	Solutia Austria Gmbh	Emulgatoren für alkydharzemulsionen mit hohem feststoffgehalt

2003
- 2003-04-21 EP EP03009114A patent/EP1471123A1/fr not_active Withdrawn
2004
- 2004-04-19 PL PL04728173T patent/PL1622986T3/pl unknown
- 2004-04-19 US US10/553,635 patent/US7479518B2/en not_active Expired - Lifetime
- 2004-04-19 CA CA2522801A patent/CA2522801C/fr not_active Expired - Fee Related
- 2004-04-19 WO PCT/EP2004/004115 patent/WO2004094546A1/fr not_active Ceased
- 2004-04-19 ES ES04728173T patent/ES2368220T3/es not_active Expired - Lifetime
- 2004-04-19 AT AT04728173T patent/ATE514762T1/de active
- 2004-04-19 EP EP04728173A patent/EP1622986B1/fr not_active Expired - Lifetime
2005
- 2005-11-18 NO NO20055469A patent/NO331887B1/no not_active IP Right Cessation

Also Published As

Publication number	Publication date
EP1622986A1 (fr)	2006-02-08
PL1622986T3 (pl)	2011-11-30
US20070167603A1 (en)	2007-07-19
CA2522801C (fr)	2012-10-30
CA2522801A1 (fr)	2004-11-04
EP1471123A1 (fr)	2004-10-27
ATE514762T1 (de)	2011-07-15
ES2368220T3 (es)	2011-11-15
EP1622986B1 (fr)	2011-06-29
US7479518B2 (en)	2009-01-20
NO20055469L (no)	2006-01-10
WO2004094546A1 (fr)	2004-11-04
NO20055469D0 (no)	2005-11-18

Legal Events

Date	Code	Title	Description
2014-04-22	CHAD	Change of the owner's name or address (par. 44 patent law, par. patentforskriften)	Owner name: ALLNEX AUSTRIA GMBH, AT
2017-11-27	MM1K	Lapsed by not paying the annual fees

Publication	Publication Date	Title
US6780910B2 (en)	2004-08-24	Alkyd resin emulsion
DK172361B1 (da)	1998-04-14	Fremgangsmåde til fremstilling af vandfortyndbare lufttørrende lakbindemidler samt anvendelse af bindemidlerne til lufttørrende vandfortyndbare lakker
JPS58191762A (ja)	1983-11-09	水ベ−スの硬質塗料組成物および製造方法
US20140256860A1 (en)	2014-09-11	Short oil alkyd resin dispersion for industrial coating compositions
US7479518B2 (en)	2009-01-20	Alkyd resin emulsions for coating varnishes
US7718731B2 (en)	2010-05-18	Aqueous dispersion of alkyde resin which is treated with an oxidizing agent and which has improved drying properties
EP1694781B1 (fr)	2019-01-30	Additif de peinture
AU772602B2 (en)	2004-05-06	Emulsions
US6121349A (en)	2000-09-19	Aqueous polyvinyl acetal dispersions
US3440193A (en)	1969-04-22	Oil-modified alkyd emulsion coatings
US6469096B1 (en)	2002-10-22	Emulsifiers for high-solids alkyd resin emulsions
JPS6254829B2 (fr)	1987-11-17
JPS61101577A (ja)	1986-05-20	水性顔料分散液
EP3953414B1 (fr)	2023-06-07	Nouvelles nanoémulsions, procédés pour leur production, et utilisations et produits associés
AT390261B (de)	1990-04-10	Verfahren zur herstellung von waessrigen, oxidativ trocknenden epoxidharzester-emulsionen und deren verwendung als bindemittel fuer luftrocknende lacke
HU189762B (en)	1986-07-28	Method dor producing air-drying adhesive emulsions
EP3548566B1 (fr)	2020-09-30	Procédé pour la préparation d'une composition de liant aqueux, composition de liant aqueux, et composition de revêtement aqueux comprenant cette composition de liant
US12630736B2 (en)	2026-05-19	Nanoemulsions, methods of their production and related uses and products
AU6711390A (en)	1991-05-31	Water-soluble resin
NO171686B (no)	1993-01-11	Belegningspreparat paa basis av en blokk-kopolymer, og en fremgangsmaate for fremstilling derav
MXPA96004325A (en)	1998-09-18	Procedure for the preparation of agglutinants of coating with air drying, diluibles with water, and the use of the mis