RU2011137471A - Водные системы покрытий на основе физически высыхающих уретанакрилатов - Google Patents
Водные системы покрытий на основе физически высыхающих уретанакрилатов Download PDFInfo
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- RU2011137471A RU2011137471A RU2011137471/04A RU2011137471A RU2011137471A RU 2011137471 A RU2011137471 A RU 2011137471A RU 2011137471/04 A RU2011137471/04 A RU 2011137471/04A RU 2011137471 A RU2011137471 A RU 2011137471A RU 2011137471 A RU2011137471 A RU 2011137471A
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- 239000011248 coating agent Substances 0.000 title claims 3
- 238000000576 coating method Methods 0.000 title claims 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 title claims 2
- 238000001035 drying Methods 0.000 title 1
- 239000006185 dispersion Substances 0.000 claims abstract 20
- 150000001252 acrylic acid derivatives Chemical class 0.000 claims abstract 19
- 239000004814 polyurethane Substances 0.000 claims abstract 15
- 229920002635 polyurethane Polymers 0.000 claims abstract 15
- -1 aliphatic diols Chemical class 0.000 claims abstract 8
- 150000001875 compounds Chemical class 0.000 claims abstract 6
- 125000003010 ionic group Chemical group 0.000 claims abstract 6
- NIXOWILDQLNWCW-UHFFFAOYSA-M acrylate group Chemical group C(C=C)(=O)[O-] NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims abstract 5
- 239000005056 polyisocyanate Substances 0.000 claims abstract 5
- 229920001228 polyisocyanate Polymers 0.000 claims abstract 5
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract 4
- 239000003085 diluting agent Substances 0.000 claims abstract 3
- 150000001298 alcohols Chemical class 0.000 claims abstract 2
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract 2
- 230000000694 effects Effects 0.000 claims abstract 2
- 229920005906 polyester polyol Polymers 0.000 claims abstract 2
- 229920005862 polyol Polymers 0.000 claims abstract 2
- 150000003077 polyols Chemical class 0.000 claims abstract 2
- 229920003009 polyurethane dispersion Polymers 0.000 claims abstract 2
- 150000003628 tricarboxylic acids Chemical class 0.000 claims abstract 2
- 239000000203 mixture Substances 0.000 claims 6
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 claims 4
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 claims 4
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims 3
- 238000000034 method Methods 0.000 claims 3
- PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 claims 2
- DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 claims 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims 2
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 claims 2
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 claims 2
- PFURGBBHAOXLIO-UHFFFAOYSA-N cyclohexane-1,2-diol Chemical compound OC1CCCCC1O PFURGBBHAOXLIO-UHFFFAOYSA-N 0.000 claims 2
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 claims 2
- NIMLQBUJDJZYEJ-UHFFFAOYSA-N isophorone diisocyanate Chemical compound CC1(C)CC(N=C=O)CC(C)(CN=C=O)C1 NIMLQBUJDJZYEJ-UHFFFAOYSA-N 0.000 claims 2
- DNIAPMSPPWPWGF-UHFFFAOYSA-N monopropylene glycol Natural products CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 claims 2
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 claims 2
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 claims 2
- 235000013772 propylene glycol Nutrition 0.000 claims 2
- 238000010526 radical polymerization reaction Methods 0.000 claims 2
- ARCGXLSVLAOJQL-UHFFFAOYSA-N trimellitic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C(C(O)=O)=C1 ARCGXLSVLAOJQL-UHFFFAOYSA-N 0.000 claims 2
- DNIAPMSPPWPWGF-VKHMYHEASA-N (+)-propylene glycol Chemical compound C[C@H](O)CO DNIAPMSPPWPWGF-VKHMYHEASA-N 0.000 claims 1
- PCHXZXKMYCGVFA-UHFFFAOYSA-N 1,3-diazetidine-2,4-dione Chemical group O=C1NC(=O)N1 PCHXZXKMYCGVFA-UHFFFAOYSA-N 0.000 claims 1
- YPFDHNVEDLHUCE-UHFFFAOYSA-N 1,3-propanediol Substances OCCCO YPFDHNVEDLHUCE-UHFFFAOYSA-N 0.000 claims 1
- 229940008841 1,6-hexamethylene diisocyanate Drugs 0.000 claims 1
- PTBDIHRZYDMNKB-UHFFFAOYSA-N 2,2-Bis(hydroxymethyl)propionic acid Chemical compound OCC(C)(CO)C(O)=O PTBDIHRZYDMNKB-UHFFFAOYSA-N 0.000 claims 1
- IVGRSQBDVIJNDA-UHFFFAOYSA-N 2-(2-aminoethylamino)ethanesulfonic acid Chemical compound NCCNCCS(O)(=O)=O IVGRSQBDVIJNDA-UHFFFAOYSA-N 0.000 claims 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims 1
- SZSSMFVYZRQGIM-UHFFFAOYSA-N 2-(hydroxymethyl)-2-propylpropane-1,3-diol Chemical compound CCCC(CO)(CO)CO SZSSMFVYZRQGIM-UHFFFAOYSA-N 0.000 claims 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims 1
- FDSUVTROAWLVJA-UHFFFAOYSA-N 2-[[3-hydroxy-2,2-bis(hydroxymethyl)propoxy]methyl]-2-(hydroxymethyl)propane-1,3-diol;prop-2-enoic acid Chemical compound OC(=O)C=C.OC(=O)C=C.OC(=O)C=C.OC(=O)C=C.OC(=O)C=C.OCC(CO)(CO)COCC(CO)(CO)CO FDSUVTROAWLVJA-UHFFFAOYSA-N 0.000 claims 1
- WVQHODUGKTXKQF-UHFFFAOYSA-N 2-ethyl-2-methylhexane-1,1-diol Chemical compound CCCCC(C)(CC)C(O)O WVQHODUGKTXKQF-UHFFFAOYSA-N 0.000 claims 1
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 claims 1
- RNLHGQLZWXBQNY-UHFFFAOYSA-N 3-(aminomethyl)-3,5,5-trimethylcyclohexan-1-amine Chemical compound CC1(C)CC(N)CC(C)(CN)C1 RNLHGQLZWXBQNY-UHFFFAOYSA-N 0.000 claims 1
- RDFQSFOGKVZWKF-UHFFFAOYSA-N 3-hydroxy-2,2-dimethylpropanoic acid Chemical compound OCC(C)(C)C(O)=O RDFQSFOGKVZWKF-UHFFFAOYSA-N 0.000 claims 1
- PJWWRFATQTVXHA-UHFFFAOYSA-N Cyclohexylaminopropanesulfonic acid Chemical compound OS(=O)(=O)CCCNC1CCCCC1 PJWWRFATQTVXHA-UHFFFAOYSA-N 0.000 claims 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical group C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims 1
- UEEJHVSXFDXPFK-UHFFFAOYSA-N N-dimethylaminoethanol Chemical compound CN(C)CCO UEEJHVSXFDXPFK-UHFFFAOYSA-N 0.000 claims 1
- LGRFSURHDFAFJT-UHFFFAOYSA-N Phthalic anhydride Natural products C1=CC=C2C(=O)OC(=O)C2=C1 LGRFSURHDFAFJT-UHFFFAOYSA-N 0.000 claims 1
- 229920002873 Polyethylenimine Polymers 0.000 claims 1
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical group CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 claims 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 claims 1
- HVVWZTWDBSEWIH-UHFFFAOYSA-N [2-(hydroxymethyl)-3-prop-2-enoyloxy-2-(prop-2-enoyloxymethyl)propyl] prop-2-enoate Chemical compound C=CC(=O)OCC(CO)(COC(=O)C=C)COC(=O)C=C HVVWZTWDBSEWIH-UHFFFAOYSA-N 0.000 claims 1
- 239000002253 acid Substances 0.000 claims 1
- 150000007513 acids Chemical class 0.000 claims 1
- 239000000853 adhesive Substances 0.000 claims 1
- 230000001070 adhesive effect Effects 0.000 claims 1
- 229920003180 amino resin Polymers 0.000 claims 1
- 150000008064 anhydrides Chemical class 0.000 claims 1
- 230000015572 biosynthetic process Effects 0.000 claims 1
- OHJMTUPIZMNBFR-UHFFFAOYSA-N biuret Chemical compound NC(=O)NC(N)=O OHJMTUPIZMNBFR-UHFFFAOYSA-N 0.000 claims 1
- JHIWVOJDXOSYLW-UHFFFAOYSA-N butyl 2,2-difluorocyclopropane-1-carboxylate Chemical compound CCCCOC(=O)C1CC1(F)F JHIWVOJDXOSYLW-UHFFFAOYSA-N 0.000 claims 1
- 150000001718 carbodiimides Chemical class 0.000 claims 1
- 239000004359 castor oil Substances 0.000 claims 1
- 235000019438 castor oil Nutrition 0.000 claims 1
- 238000006243 chemical reaction Methods 0.000 claims 1
- PMMYEEVYMWASQN-IMJSIDKUSA-N cis-4-Hydroxy-L-proline Chemical compound O[C@@H]1CN[C@H](C(O)=O)C1 PMMYEEVYMWASQN-IMJSIDKUSA-N 0.000 claims 1
- 239000003431 cross linking reagent Substances 0.000 claims 1
- KORSJDCBLAPZEQ-UHFFFAOYSA-N dicyclohexylmethane-4,4'-diisocyanate Chemical compound C1CC(N=C=O)CCC1CC1CCC(N=C=O)CC1 KORSJDCBLAPZEQ-UHFFFAOYSA-N 0.000 claims 1
- 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 claims 1
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 claims 1
- 125000001841 imino group Chemical group [H]N=* 0.000 claims 1
- 150000002500 ions Chemical group 0.000 claims 1
- HLJDOURGTRAFHE-UHFFFAOYSA-N isocyanic acid;3,5,5-trimethylcyclohex-2-en-1-one Chemical compound N=C=O.N=C=O.CC1=CC(=O)CC(C)(C)C1 HLJDOURGTRAFHE-UHFFFAOYSA-N 0.000 claims 1
- ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Chemical compound OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- CRVGTESFCCXCTH-UHFFFAOYSA-N methyl diethanolamine Chemical compound OCCN(C)CCO CRVGTESFCCXCTH-UHFFFAOYSA-N 0.000 claims 1
- 230000003472 neutralizing effect Effects 0.000 claims 1
- WWLCIARIZCNJPT-UHFFFAOYSA-N oxiran-2-ylmethyl 2-ethyl-2-methylheptanoate Chemical compound CCCCCC(C)(CC)C(=O)OCC1CO1 WWLCIARIZCNJPT-UHFFFAOYSA-N 0.000 claims 1
- 229920000233 poly(alkylene oxides) Polymers 0.000 claims 1
- 229920000166 polytrimethylene carbonate Polymers 0.000 claims 1
- 239000000126 substance Substances 0.000 claims 1
- 239000000758 substrate Substances 0.000 claims 1
- 238000003786 synthesis reaction Methods 0.000 claims 1
- QXJQHYBHAIHNGG-UHFFFAOYSA-N trimethylolethane Chemical compound OCC(C)(CO)CO QXJQHYBHAIHNGG-UHFFFAOYSA-N 0.000 claims 1
- AVWRKZWQTYIKIY-UHFFFAOYSA-N urea-1-carboxylic acid Chemical compound NC(=O)NC(O)=O AVWRKZWQTYIKIY-UHFFFAOYSA-N 0.000 claims 1
- 239000002966 varnish Substances 0.000 claims 1
- 230000005855 radiation Effects 0.000 abstract 2
Classifications
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D175/00—Coating compositions based on polyureas or polyurethanes; Coating compositions based on derivatives of such polymers
- C09D175/04—Polyurethanes
- C09D175/14—Polyurethanes having carbon-to-carbon unsaturated bonds
- C09D175/16—Polyurethanes having carbon-to-carbon unsaturated bonds having terminal carbon-to-carbon unsaturated bonds
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- 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
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- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/67—Unsaturated compounds having active hydrogen
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- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F283/00—Macromolecular compounds obtained by polymerising monomers on to polymers provided for in subclass C08G
- C08F283/01—Macromolecular compounds obtained by polymerising monomers on to polymers provided for in subclass C08G on to unsaturated polyesters
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- 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
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- C08G18/0804—Manufacture of polymers containing ionic or ionogenic groups
- C08G18/0819—Manufacture of polymers containing ionic or ionogenic groups containing anionic or anionogenic groups
- C08G18/0823—Manufacture of polymers containing ionic or ionogenic groups containing anionic or anionogenic groups containing carboxylate salt groups or groups forming them
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- 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
- C08G18/08—Processes
- C08G18/10—Prepolymer processes involving reaction of isocyanates or isothiocyanates with compounds having active hydrogen in a first reaction step
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- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
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- 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
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
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- 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
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- C08G18/4205—Polycondensates having carboxylic or carbonic ester groups in the main chain containing cyclic groups
- C08G18/4208—Polycondensates having carboxylic or carbonic ester groups in the main chain containing cyclic groups containing aromatic groups
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- 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
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- C08G18/4208—Polycondensates having carboxylic or carbonic ester groups in the main chain containing cyclic groups containing aromatic groups
- C08G18/4211—Polycondensates having carboxylic or carbonic ester groups in the main chain containing cyclic groups containing aromatic groups derived from aromatic dicarboxylic acids and dialcohols
- C08G18/4213—Polycondensates having carboxylic or carbonic ester groups in the main chain containing cyclic groups containing aromatic groups derived from aromatic dicarboxylic acids and dialcohols from terephthalic acid and dialcohols
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- 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
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- C08G18/4208—Polycondensates having carboxylic or carbonic ester groups in the main chain containing cyclic groups containing aromatic groups
- C08G18/4211—Polycondensates having carboxylic or carbonic ester groups in the main chain containing cyclic groups containing aromatic groups derived from aromatic dicarboxylic acids and dialcohols
- C08G18/4219—Polycondensates having carboxylic or carbonic ester groups in the main chain containing cyclic groups containing aromatic groups derived from aromatic dicarboxylic acids and dialcohols from aromatic dicarboxylic acids and dialcohols in combination with polycarboxylic acids and/or polyhydroxy compounds which are at least trifunctional
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- 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
- C08G18/65—Low-molecular-weight compounds having active hydrogen with high-molecular-weight compounds having active hydrogen
- C08G18/66—Compounds of groups C08G18/42, C08G18/48, or C08G18/52
- C08G18/6633—Compounds of group C08G18/42
- C08G18/6659—Compounds of group C08G18/42 with compounds of group C08G18/34
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- 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
- C08G18/67—Unsaturated compounds having active hydrogen
- C08G18/671—Unsaturated compounds having only one group containing active hydrogen
- C08G18/672—Esters of acrylic or alkyl acrylic acid having only one group containing active hydrogen
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- 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
- C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
- C08G18/72—Polyisocyanates or polyisothiocyanates
- C08G18/721—Two or more polyisocyanates not provided for in one single group C08G18/73 - C08G18/80
- C08G18/724—Combination of aromatic polyisocyanates with (cyclo)aliphatic polyisocyanates
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- 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
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- C08G18/72—Polyisocyanates or polyisothiocyanates
- C08G18/74—Polyisocyanates or polyisothiocyanates cyclic
- C08G18/75—Polyisocyanates or polyisothiocyanates cyclic cycloaliphatic
- C08G18/758—Polyisocyanates or polyisothiocyanates cyclic cycloaliphatic containing two or more cycloaliphatic rings
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
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Abstract
1. Радиационно-отверждаемая водная дисперсия на основе полиуретанакрилатов (i), содержащих в качестве структурных компонентов:A) один или несколько моногидроксифункциональных спиртов, содержащих (мет)акрилатные группы,B) сложные полиэфирполиолы, которые могут быть получены из:B1) алифатических диолов с 2-4 находящимися между гидроксильными группами атомами углерода и/или алифатических триолов иB2) ароматических дикарбоновых и/или трикарбоновых кислот,C) при необходимости полиолы, отличающиеся от компонентов А и В,D) одно или несколько соединений с диспергирующим действием на полиуретановую дисперсию, которые содержат по меньшей мере одну реакционноспособную по отношению к изоцианатам группу, а также неионные группы, ионные группы или группы, способные к образованию ионных групп,Е) органические полиизоцианаты,F) при необходимости соединения, отличающиеся от компонентов A-D и содержащие по меньшей мере одну реакционноспособную по отношению к изоцианатам группу.2. Радиационно-отверждаемая водная дисперсия на основе полиуретанакрилатов (i) по п.1, дополнительно содержащая в качестве компонента (ii) реакционноспособные разбавители, содержащие по меньшей мере одну способную к радикальной полимеризации группу.3. Радиационно-отверждаемая водная дисперсия на основе полиуретанакрилатов по п.1, отличающаяся тем, что используют от 5 до 75 мас.% структурного компонента В, причем суммарное количество компонентов A-F составляет 100 мас.%.4. Радиационно-отверждаемая водная дисперсия на основе полиуретанакрилатов п.1, отличающаяся тем, что гидроксильное число структурного компонента В составляет от 20 до 500 мг КОН/г.5. Радиационно-отв�
Claims (15)
1. Радиационно-отверждаемая водная дисперсия на основе полиуретанакрилатов (i), содержащих в качестве структурных компонентов:
A) один или несколько моногидроксифункциональных спиртов, содержащих (мет)акрилатные группы,
B) сложные полиэфирполиолы, которые могут быть получены из:
B1) алифатических диолов с 2-4 находящимися между гидроксильными группами атомами углерода и/или алифатических триолов и
B2) ароматических дикарбоновых и/или трикарбоновых кислот,
C) при необходимости полиолы, отличающиеся от компонентов А и В,
D) одно или несколько соединений с диспергирующим действием на полиуретановую дисперсию, которые содержат по меньшей мере одну реакционноспособную по отношению к изоцианатам группу, а также неионные группы, ионные группы или группы, способные к образованию ионных групп,
Е) органические полиизоцианаты,
F) при необходимости соединения, отличающиеся от компонентов A-D и содержащие по меньшей мере одну реакционноспособную по отношению к изоцианатам группу.
2. Радиационно-отверждаемая водная дисперсия на основе полиуретанакрилатов (i) по п.1, дополнительно содержащая в качестве компонента (ii) реакционноспособные разбавители, содержащие по меньшей мере одну способную к радикальной полимеризации группу.
3. Радиационно-отверждаемая водная дисперсия на основе полиуретанакрилатов по п.1, отличающаяся тем, что используют от 5 до 75 мас.% структурного компонента В, причем суммарное количество компонентов A-F составляет 100 мас.%.
4. Радиационно-отверждаемая водная дисперсия на основе полиуретанакрилатов п.1, отличающаяся тем, что гидроксильное число структурного компонента В составляет от 20 до 500 мг КОН/г.
5. Радиационно-отверждаемая водная дисперсия на основе полиуретанакрилатов по п.1, отличающаяся тем, что в качестве структурного компонента А она содержит 2-гидроксиэтил(мет)акрилат, 2-гидроксипропил(мет)акрилат, триакрилат пентаэритрита, пентаакрилат дипентаэритрита, продукт присоединения сложного глицидилового эфира этилметилгептановой кислоты к (мет)акриловой кислоте и/или их технические смеси.
6. Радиационно-отверждаемая водная дисперсия на основе полиуретанакрилатов по п.1, отличающаяся тем, что в качестве компонента В1 она содержит 1,2-этандиол, 1,2-пропандиол, 1,3-пропандиол, неопентилгликоль, 2-этил-2-бутилпропандиол, 1,3-бутандиол, 1,2-цикло-гександиол, 1,4-циклогександиол, 1,4-бутандиол, триметилолэтан, триметилолпропан, триметилолбутан, глицерин и/или касторовое масло, а в качестве компонента В2 фталевую кислоту, фталевый ангидрид, изофталевую кислоту, терефталевую кислоту, тримеллитовую кислоту, ангидриды этих кислот и/или смеси указанных соединений.
7. Радиационно-отверждаемая водная дисперсия на основе полиуретанакрилатов по п.1, отличающаяся тем, что в качестве компонента В1 она содержит 1,2-этандиол, 1,2-пропандиол, неопентилгликоль и/или триметилолпропан, а в качестве компонента В2 изофталевую кислоту и/или терефталевую кислоту.
8. Радиационно-отверждаемая водная дисперсия на основе полиуре-танакрилатов по п.1, отличающаяся тем, что в качестве компонента D она содержит 2-(2-аминоэтиламино)этансульфокислоту, 3-(цикло-гексиламино)пропан-1-сульфокислоту, продукт присоединения изофорондиамина к акриловой кислоте, гидроксипивалиновую кислоту, диметилолпропионовую кислоту, триэтаноламин, трипропаноламин, N-метилдиэтаноламин, N,N-диметилэтаноламин, монофункциональные смешанные полиалкиленоксиды, содержащие ≥40 мол.% структурных единиц этиленоксида и ≤60 мол.% структурных единиц пропиленоксида, и/или смеси указанных соединений.
9. Радиационно-отверждаемая водная дисперсия на основе полиуретанакрилатов по одному из пп.1-8, отличающаяся тем, что в качестве компонента Е она содержит 1,6-гексаметилендиизоцианат, 1-изоциа-нато-3,3,5-триметил-5-изоцианатометилциклогексан (изофорондиизоцианат), 4,4'-диизоцианатодициклогексилметан, их смеси друг с другом, гомологи, соответственно олигомеры, 1-изоцианато-3,3,5-триметил-5-изоцианатометилциклогексана (изофорондиизоцианата) и 4,4'-диизоцианатодициклогексилметана с биуретовыми, карбодиимидными, изоциануратными, аллофанатными, иминооксадиазиндионовыми и/или уретдионовыми группами, смеси указанных гомологов, соответственно олигомеров, друг с другом или их смеси с указанными выше полиизоцианатами.
10. Способ получения радиационно-отверждаемой водной дисперсии на основе полиуретанакрилатов (i) по одному из пп.1-9, отличающийся тем, что сначала путем превращения компонентов A-D с компонентом Е, реализуемого в одну или несколько реакционных стадий, синтезируют полиуретанакрилатный форполимер (i), причем до, в процессе или после синтеза форполимера с целью формирования необходимых для диспергирования ионных групп можно добавлять нейтрализующее вещество, а затем путем добавления воды к форполимеру, соответственно перевода форполимера в воду, реализуют стадию диспергирования, причем до, в процессе или после диспергирования можно выполнять удлинение цепей с использованием компонента F.
11. Способ по п.10, отличающийся тем, что молярное отношение изоцианатных групп, содержащихся в компоненте Е, к реакционноспособным по отношению к изоцианатам группам, содержащимся в компонентах А, В, С и D, составляет от 0,8:1 до 2,5:1.
12. Способ по п.10 или 11, отличающийся тем, что в качестве дополнительного компонента (ii) добавляют один или несколько реакционноспособных разбавителей по меньшей мере с одной способной к радикальной полимеризации группой.
13. Применение радиационно-отверждаемой водной дисперсии по одному из пп.1-9 для изготовления покрытий, лаков или клеев.
14. Средство покрытия, содержащее предлагаемую в изобретении радиационно-отверждаемую водную дисперсию по одному из пп.1-9 на основе полиуретанакрилатов, а также сшивающие агенты на основе аминосмол, блокированных полиизоцианатов, неблокированных полиизоцианатов, полиазиридинов и/или поликарбодиимидов, и/или одну или несколько других дисперсий.
15. Подложка, покрытая средством покрытия по п.14.
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| CN116970332B (zh) * | 2023-08-01 | 2024-07-19 | 浙江利邦电器有限公司 | 一种墙壁开关用表面喷漆工艺 |
| CN118359953B (zh) * | 2024-06-19 | 2025-01-24 | 宁波天璇新材料科技有限公司 | 一种光固化涂料、光学膜及其应用 |
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| DE19934763A1 (de) | 1999-07-23 | 2001-01-25 | Herberts Gmbh & Co Kg | Wäßrige Elektrotauchlacke, deren Herstellung und Verwendung |
| US6509411B1 (en) * | 1998-12-10 | 2003-01-21 | E. I. Du Pont De Nemours And Company | Aqueous electrodeposition coating, the production and use thereof |
| DE10038958A1 (de) | 2000-08-09 | 2002-02-28 | Skw Bauwerkstoffe Deutschland | Flexibles und postformingfähiges Beschichtungssystem für Furnierholz auf Basis von Polyurethan-Dispersionen, Verfahren zu seiner Herstellung und dessen Verwendung |
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| KR100703854B1 (ko) * | 2006-01-13 | 2007-04-09 | 에스에스씨피 주식회사 | 무용제 자외선 경화형 수성 도료 조성물 |
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| CN101205288B (zh) * | 2006-12-22 | 2011-09-07 | 比亚迪股份有限公司 | 一种聚氨酯泡沫组合物 |
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| CN101824131A (zh) * | 2010-04-15 | 2010-09-08 | 上海子元汽车零部件有限公司 | 环保型阻燃高回弹泡沫材料及其制备方法 |
-
2009
- 2009-02-13 DE DE102009008950A patent/DE102009008950A1/de not_active Withdrawn
-
2010
- 2010-01-30 HR HRP20131212AT patent/HRP20131212T1/hr unknown
- 2010-01-30 PL PL10702610T patent/PL2396356T3/pl unknown
- 2010-01-30 SI SI201030477T patent/SI2396356T1/sl unknown
- 2010-01-30 WO PCT/EP2010/000567 patent/WO2010091797A1/de not_active Ceased
- 2010-01-30 JP JP2011549463A patent/JP2012518043A/ja active Pending
- 2010-01-30 RU RU2011137471/04A patent/RU2011137471A/ru not_active Application Discontinuation
- 2010-01-30 KR KR1020117018845A patent/KR20110126621A/ko not_active Withdrawn
- 2010-01-30 EP EP10702610.6A patent/EP2396356B1/de not_active Revoked
- 2010-01-30 DK DK10702610.6T patent/DK2396356T3/da active
- 2010-01-30 CA CA2752101A patent/CA2752101C/en not_active Expired - Fee Related
- 2010-01-30 US US13/201,074 patent/US9034985B2/en not_active Expired - Fee Related
- 2010-01-30 BR BRPI1008554A patent/BRPI1008554A2/pt not_active IP Right Cessation
- 2010-01-30 ES ES10702610T patent/ES2435802T3/es active Active
- 2010-01-30 CN CN201080007604.9A patent/CN102414233B/zh not_active Expired - Fee Related
- 2010-02-12 TW TW099104537A patent/TW201041984A/zh unknown
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RU2704812C2 (ru) * | 2014-07-31 | 2019-10-31 | Аллнэкс Аустриа Гмбх | Водные полиуретан-виниловые полимерные гибридные дисперсии |
Also Published As
| Publication number | Publication date |
|---|---|
| WO2010091797A1 (de) | 2010-08-19 |
| CN102414233A (zh) | 2012-04-11 |
| PL2396356T3 (pl) | 2014-03-31 |
| KR20110126621A (ko) | 2011-11-23 |
| CN102414233B (zh) | 2014-05-07 |
| EP2396356A1 (de) | 2011-12-21 |
| BRPI1008554A2 (pt) | 2016-03-15 |
| JP2012518043A (ja) | 2012-08-09 |
| DK2396356T3 (da) | 2014-01-13 |
| EP2396356B1 (de) | 2013-10-16 |
| ES2435802T3 (es) | 2013-12-23 |
| HRP20131212T1 (hr) | 2014-01-31 |
| CA2752101C (en) | 2018-07-17 |
| CA2752101A1 (en) | 2010-08-19 |
| TW201041984A (en) | 2010-12-01 |
| SI2396356T1 (sl) | 2014-02-28 |
| US9034985B2 (en) | 2015-05-19 |
| DE102009008950A1 (de) | 2010-08-19 |
| US20120041145A1 (en) | 2012-02-16 |
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| FA92 | Acknowledgement of application withdrawn (lack of supplementary materials submitted) |
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