SK17572002A3 - Vodný spojivový prípravok a náterový prípravok s jeho obsahom - Google Patents

Vodný spojivový prípravok a náterový prípravok s jeho obsahom Download PDF

Info

Publication number: SK17572002A3
Authority: SK; Slovakia
Prior art keywords: aqueous binder; binder composition; acid; composition according; aqueous
Prior art date: 2000-06-13

Application number

SK1757-2002A

Other languages

English (en)

Slovak (sk)

Inventor

Francis Jean Roger Loos

Genevieve H�Lene Christiane Delaunoit

Dirk Emiel Paula Mestach

Original Assignee

Akzo Nobel N.V.

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.)

2000-06-13

Filing date

2001-06-08

Publication date

2003-05-02

Family has litigation

First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=8171623&utm_source=***_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=SK17572002(A3) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.

2001-06-08 Application filed by Akzo Nobel N.V. filed Critical Akzo Nobel N.V.

2003-05-02 Publication of SK17572002A3 publication Critical patent/SK17572002A3/sk

Links

239000000203 mixture Substances 0.000 title claims abstract description 51
239000011230 binding agent Substances 0.000 title claims abstract description 20
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 title abstract description 41
239000000178 monomer Substances 0.000 claims abstract description 33
239000008199 coating composition Substances 0.000 claims abstract description 11
HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims abstract description 8
239000006185 dispersion Substances 0.000 claims abstract description 8
229910052723 transition metal Inorganic materials 0.000 claims abstract description 8
150000003624 transition metals Chemical class 0.000 claims abstract description 8
229910052725 zinc Inorganic materials 0.000 claims abstract description 8
239000011701 zinc Substances 0.000 claims abstract description 8
229920006243 acrylic copolymer Polymers 0.000 claims abstract description 5
YAMHXTCMCPHKLN-UHFFFAOYSA-N imidazolidin-2-one Chemical group O=C1NCCN1 YAMHXTCMCPHKLN-UHFFFAOYSA-N 0.000 claims abstract description 5
CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims description 9
239000002253 acid Substances 0.000 claims description 7
-1 cycloalkyl ester Chemical class 0.000 claims description 7
MGPYDQFQAJEDIG-UHFFFAOYSA-N ethene;urea Chemical group C=C.NC(N)=O MGPYDQFQAJEDIG-UHFFFAOYSA-N 0.000 claims description 6
150000001875 compounds Chemical class 0.000 claims description 5
238000002360 preparation method Methods 0.000 claims description 5
150000008064 anhydrides Chemical class 0.000 claims description 4
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 4
SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims description 3
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 3
150000004820 halides Chemical class 0.000 claims description 3
150000002825 nitriles Chemical class 0.000 claims description 3
229920002554 vinyl polymer Polymers 0.000 claims description 3
125000000217 alkyl group Chemical group 0.000 claims 2
150000001735 carboxylic acids Chemical class 0.000 claims 1
239000002023 wood Substances 0.000 abstract description 20
239000000758 substrate Substances 0.000 abstract description 11
150000001732 carboxylic acid derivatives Chemical class 0.000 abstract description 6
238000000576 coating method Methods 0.000 description 24
239000004815 dispersion polymer Substances 0.000 description 20
239000000243 solution Substances 0.000 description 18
229920001864 tannin Polymers 0.000 description 13
239000001648 tannin Substances 0.000 description 13
235000018553 tannin Nutrition 0.000 description 13
229920000642 polymer Polymers 0.000 description 12
239000011248 coating agent Substances 0.000 description 11
NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 9
QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 9
239000000839 emulsion Substances 0.000 description 9
ROOXNKNUYICQNP-UHFFFAOYSA-N ammonium persulfate Chemical compound [NH4+].[NH4+].[O-]S(=O)(=O)OOS([O-])(=O)=O ROOXNKNUYICQNP-UHFFFAOYSA-N 0.000 description 6
230000000903 blocking effect Effects 0.000 description 6
238000000034 method Methods 0.000 description 6
239000000049 pigment Substances 0.000 description 6
241001250616 Intsia palembanica Species 0.000 description 5
VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 4
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 4
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 4
235000011114 ammonium hydroxide Nutrition 0.000 description 4
239000007864 aqueous solution Substances 0.000 description 4
238000009472 formulation Methods 0.000 description 4
238000000227 grinding Methods 0.000 description 4
239000002904 solvent Substances 0.000 description 4
CIHOLLKRGTVIJN-UHFFFAOYSA-N tert‐butyl hydroperoxide Chemical compound CC(C)(C)OO CIHOLLKRGTVIJN-UHFFFAOYSA-N 0.000 description 4
239000012855 volatile organic compound Substances 0.000 description 4
DAFHKNAQFPVRKR-UHFFFAOYSA-N (3-hydroxy-2,2,4-trimethylpentyl) 2-methylpropanoate Chemical compound CC(C)C(O)C(C)(C)COC(=O)C(C)C DAFHKNAQFPVRKR-UHFFFAOYSA-N 0.000 description 3
OVSKIKFHRZPJSS-UHFFFAOYSA-N 2,4-D Chemical compound OC(=O)COC1=CC=C(Cl)C=C1Cl OVSKIKFHRZPJSS-UHFFFAOYSA-N 0.000 description 3
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 3
229910021529 ammonia Inorganic materials 0.000 description 3
229910001870 ammonium persulfate Inorganic materials 0.000 description 3
239000000945 filler Substances 0.000 description 3
239000011148 porous material Substances 0.000 description 3
CYUZOYPRAQASLN-UHFFFAOYSA-N 3-prop-2-enoyloxypropanoic acid Chemical compound OC(=O)CCOC(=O)C=C CYUZOYPRAQASLN-UHFFFAOYSA-N 0.000 description 2
HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 2
NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonium chloride Substances [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 2
KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-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
RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 2
UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
DMSMPAJRVJJAGA-UHFFFAOYSA-N benzo[d]isothiazol-3-one Chemical compound C1=CC=C2C(=O)NSC2=C1 DMSMPAJRVJJAGA-UHFFFAOYSA-N 0.000 description 2
CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 2
125000002091 cationic group Chemical group 0.000 description 2
239000011247 coating layer Substances 0.000 description 2
230000000052 comparative effect Effects 0.000 description 2
238000005260 corrosion Methods 0.000 description 2
230000007797 corrosion Effects 0.000 description 2
HHICRQHZPBOQPI-UHFFFAOYSA-L diazanium;zinc;dicarbonate Chemical compound [NH4+].[NH4+].[Zn+2].[O-]C([O-])=O.[O-]C([O-])=O HHICRQHZPBOQPI-UHFFFAOYSA-L 0.000 description 2
238000002845 discoloration Methods 0.000 description 2
238000001035 drying Methods 0.000 description 2
238000007720 emulsion polymerization reaction Methods 0.000 description 2
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
125000000524 functional group Chemical group 0.000 description 2
230000009477 glass transition Effects 0.000 description 2
239000004615 ingredient Substances 0.000 description 2
239000003999 initiator Substances 0.000 description 2
239000010410 layer Substances 0.000 description 2
229910052757 nitrogen Inorganic materials 0.000 description 2
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 2
239000000123 paper Substances 0.000 description 2
239000002245 particle Substances 0.000 description 2
239000007787 solid Substances 0.000 description 2
VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 2
230000002087 whitening effect Effects 0.000 description 2
DTGKSKDOIYIVQL-WEDXCCLWSA-N (+)-borneol Chemical group C1C[C@@]2(C)[C@@H](O)C[C@@H]1C2(C)C DTGKSKDOIYIVQL-WEDXCCLWSA-N 0.000 description 1
GSSDUXHQPXODCN-UHFFFAOYSA-N 1-phenylethenylphosphonic acid Chemical compound OP(O)(=O)C(=C)C1=CC=CC=C1 GSSDUXHQPXODCN-UHFFFAOYSA-N 0.000 description 1
LCPVQAHEFVXVKT-UHFFFAOYSA-N 2-(2,4-difluorophenoxy)pyridin-3-amine Chemical compound NC1=CC=CN=C1OC1=CC=C(F)C=C1F LCPVQAHEFVXVKT-UHFFFAOYSA-N 0.000 description 1
JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 description 1
OEPOKWHJYJXUGD-UHFFFAOYSA-N 2-(3-phenylmethoxyphenyl)-1,3-thiazole-4-carbaldehyde Chemical compound O=CC1=CSC(C=2C=C(OCC=3C=CC=CC=3)C=CC=2)=N1 OEPOKWHJYJXUGD-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
PGKQTZHDCHKDQK-UHFFFAOYSA-N 2-phenylethenylphosphonic acid Chemical compound OP(O)(=O)C=CC1=CC=CC=C1 PGKQTZHDCHKDQK-UHFFFAOYSA-N 0.000 description 1
FGLXTRRGELKYNO-UHFFFAOYSA-N 4-hydroxy-2-methylidenepentanoic acid Chemical compound CC(O)CC(=C)C(O)=O FGLXTRRGELKYNO-UHFFFAOYSA-N 0.000 description 1
NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
ATRRKUHOCOJYRX-UHFFFAOYSA-N Ammonium bicarbonate Chemical compound [NH4+].OC([O-])=O ATRRKUHOCOJYRX-UHFFFAOYSA-N 0.000 description 1
CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Natural products OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 1
LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 1
GAWIXWVDTYZWAW-UHFFFAOYSA-N C[CH]O Chemical group C[CH]O GAWIXWVDTYZWAW-UHFFFAOYSA-N 0.000 description 1
CIWBSHSKHKDKBQ-DUZGATOHSA-N D-isoascorbic acid Chemical compound OC[C@@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-DUZGATOHSA-N 0.000 description 1
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 1
229910019142 PO4 Inorganic materials 0.000 description 1
NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 1
239000004793 Polystyrene Substances 0.000 description 1
OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
229920013802 TRITON CF-10 Polymers 0.000 description 1
XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
230000002378 acidificating effect Effects 0.000 description 1
150000007513 acids Chemical class 0.000 description 1
150000003926 acrylamides Chemical class 0.000 description 1
NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
150000001253 acrylic acids Chemical class 0.000 description 1
125000005907 alkyl ester group Chemical group 0.000 description 1
XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 description 1
125000003277 amino group Chemical group 0.000 description 1
239000001099 ammonium carbonate Substances 0.000 description 1
235000012501 ammonium carbonate Nutrition 0.000 description 1
239000000908 ammonium hydroxide Substances 0.000 description 1
150000003863 ammonium salts Chemical class 0.000 description 1
238000013459 approach Methods 0.000 description 1
239000013011 aqueous formulation Substances 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
230000001680 brushing effect Effects 0.000 description 1
125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 1
125000002843 carboxylic acid group Chemical group 0.000 description 1
150000001734 carboxylic acid salts Chemical class 0.000 description 1
239000011111 cardboard Substances 0.000 description 1
238000006243 chemical reaction Methods 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
HNEGQIOMVPPMNR-IHWYPQMZSA-N citraconic acid Chemical compound OC(=O)C(/C)=C\C(O)=O HNEGQIOMVPPMNR-IHWYPQMZSA-N 0.000 description 1
229940018557 citraconic acid Drugs 0.000 description 1
238000005345 coagulation Methods 0.000 description 1
230000015271 coagulation Effects 0.000 description 1
229920001577 copolymer Polymers 0.000 description 1
238000007334 copolymerization reaction Methods 0.000 description 1
125000000753 cycloalkyl group Chemical group 0.000 description 1
125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
SWXVUIWOUIDPGS-UHFFFAOYSA-N diacetone alcohol Chemical compound CC(=O)CC(C)(C)O SWXVUIWOUIDPGS-UHFFFAOYSA-N 0.000 description 1
150000001993 dienes Chemical class 0.000 description 1
235000014113 dietary fatty acids Nutrition 0.000 description 1
239000003480 eluent Substances 0.000 description 1
238000004945 emulsification Methods 0.000 description 1
230000007613 environmental effect Effects 0.000 description 1
235000010350 erythorbic acid Nutrition 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
XUCNUKMRBVNAPB-UHFFFAOYSA-N fluoroethene Chemical compound FC=C XUCNUKMRBVNAPB-UHFFFAOYSA-N 0.000 description 1
239000001530 fumaric acid Substances 0.000 description 1
238000005227 gel permeation chromatography Methods 0.000 description 1
238000001879 gelation Methods 0.000 description 1
229920001519 homopolymer Polymers 0.000 description 1
125000004356 hydroxy functional group Chemical group O* 0.000 description 1
125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
229940026239 isoascorbic acid Drugs 0.000 description 1
VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
239000011976 maleic acid Substances 0.000 description 1
FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
125000002496 methyl group Chemical group [H]C([H])([H])* 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
230000005012 migration Effects 0.000 description 1
238000013508 migration Methods 0.000 description 1
238000002156 mixing Methods 0.000 description 1
125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
230000003472 neutralizing effect Effects 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
239000010452 phosphate Substances 0.000 description 1
ABLZXFCXXLZCGV-UHFFFAOYSA-N phosphonic acid group Chemical group P(O)(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 description 1
229920002223 polystyrene Polymers 0.000 description 1
HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical compound C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 description 1
238000010526 radical polymerization reaction Methods 0.000 description 1
XWGJFPHUCFXLBL-UHFFFAOYSA-M rongalite Chemical compound [Na+].OCS([O-])=O XWGJFPHUCFXLBL-UHFFFAOYSA-M 0.000 description 1
229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
235000017557 sodium bicarbonate Nutrition 0.000 description 1
CHQMHPLRPQMAMX-UHFFFAOYSA-L sodium persulfate Substances [Na+].[Na+].[O-]S(=O)(=O)OOS([O-])(=O)=O CHQMHPLRPQMAMX-UHFFFAOYSA-L 0.000 description 1
238000003756 stirring Methods 0.000 description 1
YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
229910001428 transition metal ion Inorganic materials 0.000 description 1
229920001567 vinyl ester resin Polymers 0.000 description 1
239000011787 zinc oxide 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
- 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
- C09D133/064—Copolymers with monomers not covered by C09D133/06 containing anhydride, COOH or COOM groups, with M being metal or onium-cation
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31855—Of addition polymer from unsaturated monomers
- Y10T428/3188—Next to cellulosic

Landscapes

Chemical & Material Sciences (AREA)
Life Sciences & Earth Sciences (AREA)
Engineering & Computer Science (AREA)
Materials Engineering (AREA)
Wood Science & Technology (AREA)
Organic Chemistry (AREA)
Paints Or Removers (AREA)
Curing Cements, Concrete, And Artificial Stone (AREA)
Adhesives Or Adhesive Processes (AREA)
Materials Applied To Surfaces To Minimize Adherence Of Mist Or Water (AREA)
Nonmetallic Welding Materials (AREA)
Laminated Bodies (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)

SK1757-2002A 2000-06-13 2001-06-08 Vodný spojivový prípravok a náterový prípravok s jeho obsahom SK17572002A3 (sk)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
EP00202056		2000-06-13
PCT/EP2001/006461 WO2001096485A1 (en)	2000-06-13	2001-06-08	Water borne binder composition

Publications (1)

Publication Number	Publication Date
SK17572002A3 true SK17572002A3 (sk)	2003-05-02

Family

ID=8171623

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
SK1757-2002A SK17572002A3 (sk)	2000-06-13	2001-06-08	Vodný spojivový prípravok a náterový prípravok s jeho obsahom

Country Status (18)

Country	Link
US (1)	US6660788B2 (no)
EP (1)	EP1294816B1 (no)
CN (1)	CN1175071C (no)
AT (1)	ATE316127T1 (no)
AU (1)	AU2001266053A1 (no)
BG (1)	BG107318A (no)
CZ (1)	CZ294590B6 (no)
DE (1)	DE60116767T2 (no)
DK (1)	DK1294816T3 (no)
EE (1)	EE200200691A (no)
ES (1)	ES2254441T3 (no)
HU (1)	HUP0301115A3 (no)
NO (1)	NO20025939D0 (no)
PL (1)	PL204609B1 (no)
PT (1)	PT1294816E (no)
RU (1)	RU2278883C2 (no)
SK (1)	SK17572002A3 (no)
WO (1)	WO2001096485A1 (no)

Families Citing this family (16)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
WO2008002495A2 (en) *	2006-06-23	2008-01-03	The Sherwin-Williams Company	High solids emulsions
PT2158226E (pt)	2007-06-11	2012-12-27	Basf Se	Método para a preparação de uma dispersão aquosa de polímero
EP2169080B1 (en) *	2008-09-12	2011-04-27	Rohm and Haas Company	Aldehyde Scrubbing in Crust Leather and Tanned Leather
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2001
- 2001-06-08 PT PT01943485T patent/PT1294816E/pt unknown
- 2001-06-08 AU AU2001266053A patent/AU2001266053A1/en not_active Abandoned
- 2001-06-08 PL PL365526A patent/PL204609B1/pl unknown
- 2001-06-08 SK SK1757-2002A patent/SK17572002A3/sk unknown
- 2001-06-08 DK DK01943485T patent/DK1294816T3/da active
- 2001-06-08 EE EEP200200691A patent/EE200200691A/xx unknown
- 2001-06-08 CZ CZ20024097A patent/CZ294590B6/cs not_active IP Right Cessation
- 2001-06-08 WO PCT/EP2001/006461 patent/WO2001096485A1/en active IP Right Grant
- 2001-06-08 HU HU0301115A patent/HUP0301115A3/hu unknown
- 2001-06-08 AT AT01943485T patent/ATE316127T1/de active
- 2001-06-08 CN CNB018110967A patent/CN1175071C/zh not_active Expired - Fee Related
- 2001-06-08 EP EP01943485A patent/EP1294816B1/en not_active Expired - Lifetime
- 2001-06-08 ES ES01943485T patent/ES2254441T3/es not_active Expired - Lifetime
- 2001-06-08 RU RU2003100530/04A patent/RU2278883C2/ru active
- 2001-06-08 DE DE60116767T patent/DE60116767T2/de not_active Expired - Lifetime
- 2001-06-12 US US09/879,377 patent/US6660788B2/en not_active Expired - Lifetime
2002
- 2002-11-25 BG BG107318A patent/BG107318A/bg unknown
- 2002-12-11 NO NO20025939A patent/NO20025939D0/no not_active Application Discontinuation

Also Published As

Publication number	Publication date
NO20025939L (no)	2002-12-11
DE60116767D1 (de)	2006-04-06
ATE316127T1 (de)	2006-02-15
EP1294816B1 (en)	2006-01-18
HUP0301115A3 (en)	2005-11-28
WO2001096485A1 (en)	2001-12-20
ES2254441T3 (es)	2006-06-16
PL204609B1 (pl)	2010-01-29
HUP0301115A2 (hu)	2003-07-28
BG107318A (bg)	2004-08-31
DE60116767T2 (de)	2006-11-02
PT1294816E (pt)	2006-06-30
EE200200691A (et)	2004-06-15
RU2278883C2 (ru)	2006-06-27
AU2001266053A1 (en)	2001-12-24
CZ294590B6 (cs)	2005-02-16
CN1175071C (zh)	2004-11-10
EP1294816A1 (en)	2003-03-26
PL365526A1 (en)	2005-01-10
US20020035189A1 (en)	2002-03-21
US6660788B2 (en)	2003-12-09
NO20025939D0 (no)	2002-12-11
CN1436224A (zh)	2003-08-13
DK1294816T3 (da)	2006-05-15

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