JP6966465B2 - 組成物、水性コーティング組成物、及び水性コーティング組成物の凍結/融解安定性を改善する方法 - Google Patents
組成物、水性コーティング組成物、及び水性コーティング組成物の凍結/融解安定性を改善する方法 Download PDFInfo
- Publication number
- JP6966465B2 JP6966465B2 JP2018549950A JP2018549950A JP6966465B2 JP 6966465 B2 JP6966465 B2 JP 6966465B2 JP 2018549950 A JP2018549950 A JP 2018549950A JP 2018549950 A JP2018549950 A JP 2018549950A JP 6966465 B2 JP6966465 B2 JP 6966465B2
- Authority
- JP
- Japan
- Prior art keywords
- formula
- coating composition
- weight
- compound
- aqueous coating
- Prior art date
- 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.)
- Active
Links
- 239000008199 coating composition Substances 0.000 title claims description 78
- 239000000203 mixture Substances 0.000 title claims description 35
- 238000000034 method Methods 0.000 title claims description 30
- 230000008014 freezing Effects 0.000 title description 6
- 238000007710 freezing Methods 0.000 title description 6
- 238000010257 thawing Methods 0.000 title description 6
- 150000001875 compounds Chemical class 0.000 claims description 43
- 239000004815 dispersion polymer Substances 0.000 claims description 39
- 239000003795 chemical substances by application Substances 0.000 claims description 36
- 239000007787 solid Substances 0.000 claims description 22
- ZFOZVQLOBQUTQQ-UHFFFAOYSA-N Tributyl citrate Chemical compound CCCCOC(=O)CC(O)(C(=O)OCCCC)CC(=O)OCCCC ZFOZVQLOBQUTQQ-UHFFFAOYSA-N 0.000 claims description 10
- IBLKWZIFZMJLFL-UHFFFAOYSA-N 1-phenoxypropan-2-ol Chemical group CC(O)COC1=CC=CC=C1 IBLKWZIFZMJLFL-UHFFFAOYSA-N 0.000 claims description 7
- WMDZKDKPYCNCDZ-UHFFFAOYSA-N 2-(2-butoxypropoxy)propan-1-ol Chemical compound CCCCOC(C)COC(C)CO WMDZKDKPYCNCDZ-UHFFFAOYSA-N 0.000 claims description 7
- JDSQBDGCMUXRBM-UHFFFAOYSA-N 2-[2-(2-butoxypropoxy)propoxy]propan-1-ol Chemical compound CCCCOC(C)COC(C)COC(C)CO JDSQBDGCMUXRBM-UHFFFAOYSA-N 0.000 claims description 7
- NMBQBIACXMPEQB-UHFFFAOYSA-N 2-butoxyethyl benzoate Chemical compound CCCCOCCOC(=O)C1=CC=CC=C1 NMBQBIACXMPEQB-UHFFFAOYSA-N 0.000 claims description 7
- QCDWFXQBSFUVSP-UHFFFAOYSA-N 2-phenoxyethanol Chemical compound OCCOC1=CC=CC=C1 QCDWFXQBSFUVSP-UHFFFAOYSA-N 0.000 claims description 7
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 claims description 7
- 229920000058 polyacrylate Polymers 0.000 claims description 6
- 150000002009 diols Chemical class 0.000 claims description 3
- 238000000576 coating method Methods 0.000 description 34
- 239000003973 paint Substances 0.000 description 27
- 239000011248 coating agent Substances 0.000 description 17
- 239000000049 pigment Substances 0.000 description 16
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 14
- 229920000642 polymer Polymers 0.000 description 13
- 239000000654 additive Substances 0.000 description 12
- 239000002245 particle Substances 0.000 description 12
- 238000009472 formulation Methods 0.000 description 11
- -1 BF 3 etherate Chemical class 0.000 description 10
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 10
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 10
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 9
- 239000011230 binding agent Substances 0.000 description 8
- 239000003054 catalyst Substances 0.000 description 8
- 239000000126 substance Substances 0.000 description 7
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 6
- 239000002585 base Substances 0.000 description 6
- 239000006185 dispersion Substances 0.000 description 6
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 6
- 229910052739 hydrogen Inorganic materials 0.000 description 5
- 239000001257 hydrogen Substances 0.000 description 5
- 239000007921 spray Substances 0.000 description 5
- 239000012855 volatile organic compound Substances 0.000 description 5
- LFEHSRSSAGQWNI-UHFFFAOYSA-N 2,6,8-trimethylnonan-4-ol Polymers CC(C)CC(C)CC(O)CC(C)C LFEHSRSSAGQWNI-UHFFFAOYSA-N 0.000 description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 4
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical class CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 4
- 230000000996 additive effect Effects 0.000 description 4
- 239000012736 aqueous medium Substances 0.000 description 4
- 239000004067 bulking agent Substances 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 4
- 150000004985 diamines Chemical class 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- 239000004408 titanium dioxide Substances 0.000 description 4
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 description 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 3
- 150000001298 alcohols Chemical class 0.000 description 3
- 125000000217 alkyl group Chemical group 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 238000009826 distribution Methods 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 229920005787 opaque polymer Polymers 0.000 description 3
- 229920001568 phenolic resin Polymers 0.000 description 3
- 229920000768 polyamine Polymers 0.000 description 3
- 239000011541 reaction mixture Substances 0.000 description 3
- JCTXKRPTIMZBJT-UHFFFAOYSA-N 2,2,4-trimethylpentane-1,3-diol Chemical compound CC(C)C(O)C(C)(C)CO JCTXKRPTIMZBJT-UHFFFAOYSA-N 0.000 description 2
- QUKFNRQNPQSTPD-UHFFFAOYSA-N 2-methylpropanoic acid;pentane-1,3-diol Chemical compound CC(C)C(O)=O.CCC(O)CCO QUKFNRQNPQSTPD-UHFFFAOYSA-N 0.000 description 2
- 101100099844 Arabidopsis thaliana TMN6 gene Proteins 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- 239000004908 Emulsion polymer Substances 0.000 description 2
- 239000004593 Epoxy Substances 0.000 description 2
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 229920002125 Sokalan® Polymers 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- 229920006397 acrylic thermoplastic Polymers 0.000 description 2
- 239000002671 adjuvant Substances 0.000 description 2
- 230000001588 bifunctional effect Effects 0.000 description 2
- 239000003139 biocide Substances 0.000 description 2
- 238000004581 coalescence Methods 0.000 description 2
- 239000003086 colorant Substances 0.000 description 2
- GYZLOYUZLJXAJU-UHFFFAOYSA-N diglycidyl ether Chemical compound C1OC1COCC1CO1 GYZLOYUZLJXAJU-UHFFFAOYSA-N 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 229920001600 hydrophobic polymer Polymers 0.000 description 2
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 2
- 239000004816 latex Substances 0.000 description 2
- 229920000126 latex Polymers 0.000 description 2
- 239000002609 medium Substances 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 2
- 239000005011 phenolic resin Substances 0.000 description 2
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 2
- 229920005596 polymer binder Polymers 0.000 description 2
- 239000002491 polymer binding agent Substances 0.000 description 2
- 229920005862 polyol Polymers 0.000 description 2
- 150000003077 polyols Chemical class 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 239000000758 substrate Substances 0.000 description 2
- 239000003760 tallow Substances 0.000 description 2
- 239000005995 Aluminium silicate Substances 0.000 description 1
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 1
- FBPFZTCFMRRESA-KVTDHHQDSA-N D-Mannitol Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-KVTDHHQDSA-N 0.000 description 1
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 1
- RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 description 1
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- AVXURJPOCDRRFD-UHFFFAOYSA-N Hydroxylamine Chemical compound ON AVXURJPOCDRRFD-UHFFFAOYSA-N 0.000 description 1
- 229930195725 Mannitol Natural products 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 229920002873 Polyethylenimine Polymers 0.000 description 1
- 108010039918 Polylysine Proteins 0.000 description 1
- 229910010413 TiO 2 Inorganic materials 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- TVXBFESIOXBWNM-UHFFFAOYSA-N Xylitol Natural products OCCC(O)C(O)C(O)CCO TVXBFESIOXBWNM-UHFFFAOYSA-N 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 238000004220 aggregation Methods 0.000 description 1
- 230000002776 aggregation Effects 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000008044 alkali metal hydroxides Chemical class 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 125000002947 alkylene group Chemical group 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 229910000323 aluminium silicate Inorganic materials 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 150000001414 amino alcohols Chemical class 0.000 description 1
- 229910000410 antimony oxide Inorganic materials 0.000 description 1
- BUOSLGZEBFSUDD-BGPZCGNYSA-N bis[(1s,3s,4r,5r)-4-methoxycarbonyl-8-methyl-8-azabicyclo[3.2.1]octan-3-yl] 2,4-diphenylcyclobutane-1,3-dicarboxylate Chemical class O([C@H]1C[C@@H]2CC[C@@H](N2C)[C@H]1C(=O)OC)C(=O)C1C(C=2C=CC=CC=2)C(C(=O)O[C@@H]2[C@@H]([C@H]3CC[C@H](N3C)C2)C(=O)OC)C1C1=CC=CC=C1 BUOSLGZEBFSUDD-BGPZCGNYSA-N 0.000 description 1
- 239000000872 buffer Substances 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 239000004359 castor oil Substances 0.000 description 1
- 235000019438 castor oil Nutrition 0.000 description 1
- 239000004568 cement Substances 0.000 description 1
- 239000002738 chelating agent Substances 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 229930003836 cresol Natural products 0.000 description 1
- 125000000853 cresyl group Chemical group C1(=CC=C(C=C1)C)* 0.000 description 1
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 238000002296 dynamic light scattering Methods 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 238000007720 emulsion polymerization reaction Methods 0.000 description 1
- 239000003623 enhancer Substances 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- NHWGPUVJQFTOQX-UHFFFAOYSA-N ethyl-[2-[2-[ethyl(dimethyl)azaniumyl]ethyl-methylamino]ethyl]-dimethylazanium Chemical compound CC[N+](C)(C)CCN(C)CC[N+](C)(C)CC NHWGPUVJQFTOQX-UHFFFAOYSA-N 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- WSFSSNUMVMOOMR-UHFFFAOYSA-N formaldehyde Substances O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 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 description 1
- 150000002314 glycerols Chemical class 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 239000012760 heat stabilizer Substances 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 239000006115 industrial coating Substances 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 229910000464 lead oxide Inorganic materials 0.000 description 1
- 239000004611 light stabiliser Substances 0.000 description 1
- HCWCAKKEBCNQJP-UHFFFAOYSA-N magnesium orthosilicate Chemical compound [Mg+2].[Mg+2].[O-][Si]([O-])([O-])[O-] HCWCAKKEBCNQJP-UHFFFAOYSA-N 0.000 description 1
- 239000000391 magnesium silicate Substances 0.000 description 1
- 229910052919 magnesium silicate Inorganic materials 0.000 description 1
- 235000019792 magnesium silicate Nutrition 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 239000000594 mannitol Substances 0.000 description 1
- 235000010355 mannitol Nutrition 0.000 description 1
- HEBKCHPVOIAQTA-UHFFFAOYSA-N meso ribitol Natural products OCC(O)C(O)C(O)CO HEBKCHPVOIAQTA-UHFFFAOYSA-N 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 239000003607 modifier Substances 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 239000004570 mortar (masonry) Substances 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- ZWRUINPWMLAQRD-UHFFFAOYSA-N nonan-1-ol Polymers CCCCCCCCCO ZWRUINPWMLAQRD-UHFFFAOYSA-N 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- VTRUBDSFZJNXHI-UHFFFAOYSA-N oxoantimony Chemical compound [Sb]=O VTRUBDSFZJNXHI-UHFFFAOYSA-N 0.000 description 1
- YEXPOXQUZXUXJW-UHFFFAOYSA-N oxolead Chemical compound [Pb]=O YEXPOXQUZXUXJW-UHFFFAOYSA-N 0.000 description 1
- RUOPINZRYMFPBF-UHFFFAOYSA-N pentane-1,3-diol Chemical compound CCC(O)CCO RUOPINZRYMFPBF-UHFFFAOYSA-N 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 239000004848 polyfunctional curative Substances 0.000 description 1
- 229920000656 polylysine Polymers 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000005871 repellent Substances 0.000 description 1
- 230000002940 repellent Effects 0.000 description 1
- 238000000518 rheometry Methods 0.000 description 1
- 239000000565 sealant Substances 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 229920001909 styrene-acrylic polymer Polymers 0.000 description 1
- 150000005846 sugar alcohols Chemical group 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 238000010189 synthetic method Methods 0.000 description 1
- ISXSCDLOGDJUNJ-UHFFFAOYSA-N tert-butyl prop-2-enoate Chemical compound CC(C)(C)OC(=O)C=C ISXSCDLOGDJUNJ-UHFFFAOYSA-N 0.000 description 1
- XFNJVJPLKCPIBV-UHFFFAOYSA-N trimethylenediamine Chemical compound NCCCN XFNJVJPLKCPIBV-UHFFFAOYSA-N 0.000 description 1
- GPRLSGONYQIRFK-MNYXATJNSA-N triton Chemical compound [3H+] GPRLSGONYQIRFK-MNYXATJNSA-N 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 239000000811 xylitol Substances 0.000 description 1
- HEBKCHPVOIAQTA-SCDXWVJYSA-N xylitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)CO HEBKCHPVOIAQTA-SCDXWVJYSA-N 0.000 description 1
- 235000010447 xylitol Nutrition 0.000 description 1
- 229960002675 xylitol Drugs 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
- C09D5/00—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
- C09D5/02—Emulsion paints including aerosols
- C09D5/024—Emulsion paints including aerosols characterised by the additives
-
- 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
- C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G65/02—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring
- C08G65/26—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers and other compounds
- C08G65/2603—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers and other compounds the other compounds containing oxygen
- C08G65/2606—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers and other compounds the other compounds containing oxygen containing hydroxyl groups
- C08G65/2609—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers and other compounds the other compounds containing oxygen containing hydroxyl groups containing aliphatic hydroxyl groups
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/04—Oxygen-containing compounds
- C08K5/06—Ethers; Acetals; Ketals; Ortho-esters
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L71/00—Compositions of polyethers obtained by reactions forming an ether link in the main chain; Compositions of derivatives of such polymers
-
- 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
- C09D133/08—Homopolymers or copolymers of acrylic acid esters
-
- 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
- C09D163/00—Coating compositions based on epoxy resins; Coating compositions based on derivatives of epoxy resins
-
- 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
- C09D7/00—Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
- C09D7/20—Diluents or solvents
-
- 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
- C09D7/00—Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
- C09D7/40—Additives
- C09D7/60—Additives non-macromolecular
- C09D7/63—Additives non-macromolecular organic
-
- 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
- C09D7/00—Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
- C09D7/40—Additives
- C09D7/65—Additives macromolecular
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2201/00—Properties
- C08L2201/50—Aqueous dispersion, e.g. containing polymers with a glass transition temperature (Tg) above 20°C
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Dispersion Chemistry (AREA)
- Paints Or Removers (AREA)
Description
式2の化合物、
組成物は、30重量%〜70重量%の式1及び30重量%〜70重量%の式2を含む。
式1の化合物
式2の化合物
30重量%〜70重量%の式1及び30重量%〜70重量%の式2を含む組成物に関する。いくつかの実施形態では、n=5〜10であり、他の実施形態ではn=6〜8であり、さらに他の実施形態ではn=8である。このような組成物は、いくつかの実施形態では、水性コーティング組成物、例えば塗料または他のコーティングに添加剤として提供することができる。
PVC(%)=(顔料の体積、+増量剤体積×100)/(塗料の総乾燥体積)。
水性ポリマー分散体のポリマー含有量に基づいて34重量%の固形分及び8重量%の合体剤レベルを含有する2ガロンのベース塗料配合物のバッチを表1に記載のように調製する:
(態様)
(態様1)
水性ポリマー分散体を含む水性コーティング組成物の凍結/融解安定性を改善する方法であって、式1の化合物を前記水性コーティング組成物に添加することを含み、
(態様2)
n=5〜10である、態様1に記載の方法。
(態様3)
n=6〜8である、態様1に記載の方法。
(態様4)
前記ポリマー分散体の固形分の重量に基づいて、5〜10重量%の式1が添加される、態様1〜3のいずれかに記載の方法。
(態様5)
前記ポリマー分散体固形分の重量に基づいて、6〜8重量%の式1が添加される、態様1〜4のいずれかに記載の方法。
(態様6)
前記水性コーティング組成物に少なくとも1つの合体剤を添加することをさらに含む、態様1〜5のいずれかに記載の方法。
(態様7)
前記合体剤は、式2の化合物を含む、態様6に記載の方法。
前記合体剤は、プロピレングリコールフェニルエーテル、エチレングリコールフェニルエーテル、ジプロピレングリコールn−ブチルエーテル、エチレングリコールn−ブチルエーテルベンゾエート、トリプロピレングリコールn−ブチルエーテル、2,2,4−トリメチル−1,3−ペンタンジオールモノイソブチレート、トリエチレングリコールビス−2−エチルヘキサノエート、及びトリブチルシトレートのうちの少なくとも1つを含む、態様6に記載の方法。
(態様9)
前記ポリマー分散体固形分の重量に基づいて、2〜12重量%の式2が添加される、態様6〜8のいずれかに記載の方法。
(態様10)
前記水性ポリマー分散体はアクリルポリマーを含む、態様1〜9のいずれかに記載の方法。
(態様11)
前記水性コーティング組成物に1つ以上のポリアルコキシレートを添加することをさら
に含む、態様1〜10のいずれかに記載の方法。
(態様12)
水性ポリマー分散体及び式1の化合物を含む水性コーティング組成物であって、
(態様13)
n=5〜10である、態様12に記載のコーティング組成物。
(態様14)
n=6〜8である、態様12に記載のコーティング組成物。
(態様15)
前記コーティング組成物は、前記ポリマー分散体固形分の重量に基づいて6〜8重量%の式1を含む、態様12〜14のいずれかに記載のコーティング組成物。
(態様16)
少なくとも1つの合体剤をさらに含む、態様12〜15のいずれかに記載のコーティング組成物。
(態様17)
前記合体剤は、式2の化合物を含む、態様16に記載のコーティング組成物。
前記合体剤は、プロピレングリコールフェニルエーテル、エチレングリコールフェニルエーテル、ジプロピレングリコールn−ブチルエーテル、エチレングリコールn−ブチルエーテルベンゾエート、トリプロピレングリコールn−ブチルエーテル、2,2,4−トリメチル−1,3−ペンタンジオールモノイソブチレート、トリエチレングリコールビス−2−エチルヘキサノエート、及びトリブチルシトレートのうちの少なくとも1つを含む、態様16に記載のコーティング組成物。
(態様19)
前記コーティング組成物は、前記ポリマー分散体固形分の重量に基づいて2〜12重量%の式2を含む、態様16〜18のいずれかに記載のコーティング組成物。
(態様20)
前記水性ポリマー分散体はアクリルポリマーを含む、態様12〜19のいずれかに記載のコーティング組成物。
(態様21)
1つ以上のポリアルコキシレートをさらに含む、態様12〜20のいずれかに記載のコーティング組成物。
(態様22)
式1の化合物
式2の化合物
(態様23)
n=5〜10である、態様22に記載の組成物。
(態様24)
n=6〜8である、態様22に記載の組成物。
Claims (7)
- 水性ポリマー分散体を含む水性コーティング組成物の凍結/融解安定性を改善する方法であって、式1の化合物を前記水性コーティング組成物に添加することを含み、
前記水性コーティング組成物に少なくとも1つの合体剤を添加することをさらに含み、前記合体剤は、式2の化合物を含むか、
- 前記ポリマー分散体の固形分の重量に基づいて、5〜10重量%の式1の化合物が添加される、請求項1に記載の方法。
- 前記水性ポリマー分散体はアクリルポリマーを含む、請求項1〜2のいずれかに記載の方法。
- 少なくとも1つの合体剤と水性ポリマー分散体と式1の化合物とを含む水性コーティング組成物であって、
前記合体剤は、式2の化合物を含むか、
- n=5〜10である、請求項4に記載のコーティング組成物。
- 前記水性ポリマー分散体はアクリルポリマーを含む、請求項4〜5のいずれかに記載のコーティング組成物。
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201662313984P | 2016-03-28 | 2016-03-28 | |
US62/313,984 | 2016-03-28 | ||
PCT/US2017/023382 WO2017172411A1 (en) | 2016-03-28 | 2017-03-21 | Compositions, aqueous coating compositions, and methods for improving the freeze/thaw stability of aqueous coating compositions |
Publications (2)
Publication Number | Publication Date |
---|---|
JP2019516814A JP2019516814A (ja) | 2019-06-20 |
JP6966465B2 true JP6966465B2 (ja) | 2021-11-17 |
Family
ID=58464665
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2018549950A Active JP6966465B2 (ja) | 2016-03-28 | 2017-03-21 | 組成物、水性コーティング組成物、及び水性コーティング組成物の凍結/融解安定性を改善する方法 |
Country Status (8)
Country | Link |
---|---|
US (1) | US20210222015A1 (ja) |
EP (1) | EP3436533B1 (ja) |
JP (1) | JP6966465B2 (ja) |
CN (1) | CN108779349A (ja) |
BR (1) | BR112018069115A8 (ja) |
CA (1) | CA3018979A1 (ja) |
ES (1) | ES2865029T3 (ja) |
WO (1) | WO2017172411A1 (ja) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2019174021A1 (en) | 2018-03-16 | 2019-09-19 | Dow Global Technologies Llc | Aqueous coating compositions and methods for improving freeze/thaw stability of aqueous coating compositions |
US20210087425A1 (en) * | 2018-06-06 | 2021-03-25 | Dow Global Technologies Llc | Aqueous coating composition |
ES2985579T3 (es) | 2019-04-16 | 2024-11-06 | Dow Global Technologies Llc | Composición aditiva de congelación-descongelación |
WO2021195930A1 (en) * | 2020-03-31 | 2021-10-07 | Dow Global Technologies Llc | Aqueous coating compositions |
Family Cites Families (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3634285A (en) * | 1969-03-24 | 1972-01-11 | Stauffer Wacker Silicone Corp | Silicone release emulsion |
US4111878A (en) * | 1976-08-05 | 1978-09-05 | Gaf Corporation | Water based ink composition for vinyl flooring |
US5017221A (en) * | 1989-12-05 | 1991-05-21 | Dow Corning Corporation | Polymethylalkylsiloxane emulsions and methods |
WO1994004259A1 (en) * | 1992-08-17 | 1994-03-03 | Ppg Industries, Inc. | Polysiloxane emulsions |
EP0739929A3 (en) * | 1995-04-27 | 1997-07-02 | Dow Corning | Latex from polysiloxanes emulsified directly in the presence of selected surfactants and having improved physical properties |
JPH11263936A (ja) * | 1998-03-18 | 1999-09-28 | Toagosei Co Ltd | 被覆用組成物 |
US7705082B2 (en) * | 2005-04-22 | 2010-04-27 | Basf Se | Low-VOC emulsion polymer coating compositions |
EP2426155B2 (en) * | 2010-09-03 | 2017-06-28 | Rohm and Haas Company | Multistage emulsion polymer and improved pigment efficiency |
EP3178891B1 (en) * | 2011-04-08 | 2020-10-21 | Rohm And Haas Company | Low/zero voc glycol ether-esters as coalescents for aqueous polymeric dispersions |
CN103753925B (zh) * | 2013-12-27 | 2016-08-17 | 四川东方绝缘材料股份有限公司 | 一种丙烯酸型涂层低水汽透过率聚酯薄膜及其制备方法 |
US9284469B2 (en) * | 2014-04-30 | 2016-03-15 | Xerox Corporation | Film-forming hydrophilic polymers for transfix printing process |
-
2017
- 2017-03-21 JP JP2018549950A patent/JP6966465B2/ja active Active
- 2017-03-21 CN CN201780019027.7A patent/CN108779349A/zh active Pending
- 2017-03-21 US US16/081,672 patent/US20210222015A1/en not_active Abandoned
- 2017-03-21 EP EP17715335.0A patent/EP3436533B1/en active Active
- 2017-03-21 CA CA3018979A patent/CA3018979A1/en active Pending
- 2017-03-21 ES ES17715335T patent/ES2865029T3/es active Active
- 2017-03-21 WO PCT/US2017/023382 patent/WO2017172411A1/en active Application Filing
- 2017-03-21 BR BR112018069115A patent/BR112018069115A8/pt active Search and Examination
Also Published As
Publication number | Publication date |
---|---|
US20210222015A1 (en) | 2021-07-22 |
CN108779349A (zh) | 2018-11-09 |
CA3018979A1 (en) | 2017-10-05 |
BR112018069115A2 (pt) | 2019-01-22 |
EP3436533B1 (en) | 2021-02-24 |
EP3436533A1 (en) | 2019-02-06 |
ES2865029T3 (es) | 2021-10-14 |
BR112018069115A8 (pt) | 2022-08-02 |
WO2017172411A1 (en) | 2017-10-05 |
JP2019516814A (ja) | 2019-06-20 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JP6966465B2 (ja) | 組成物、水性コーティング組成物、及び水性コーティング組成物の凍結/融解安定性を改善する方法 | |
JP6985285B2 (ja) | 組成物、水性コーティング組成物、及び水性コーティング組成物の凍結/融解安定性を改善する方法 | |
CN109923134B (zh) | 水性涂料组合物 | |
CA2717888A1 (en) | Aqueous coating compositions exhibiting increased open time with reduced levels of volatile organic compounds | |
CA2960249A1 (en) | Aqueous compositions having polyalkoxylates for improved open time | |
US20230075575A1 (en) | Aqueous coating compositions | |
CN111836861B (zh) | 水性涂料组合物和用于改善水性涂料组合物的冻融稳定性的方法 | |
CA2968012A1 (en) | Coating composition with rheology modifier | |
CA3157425A1 (en) | Coating composition and use thereof | |
TW202346493A (zh) | 水性塗料組成物 | |
WO2025039831A1 (en) | 1k coating composition and coated article | |
EP3956405B1 (en) | Freeze-thaw additive composition | |
US8728625B2 (en) | Water reducible coating compositions including carboxy ester ketals, methods of manufacture, and uses thereof | |
EP4511429A1 (en) | Aqueous coating compositions | |
WO2024243836A1 (en) | Latex polymer dispersion and the aqueous coating composition prepared from the same |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20181002 |
|
RD03 | Notification of appointment of power of attorney |
Free format text: JAPANESE INTERMEDIATE CODE: A7423 Effective date: 20181017 |
|
RD04 | Notification of resignation of power of attorney |
Free format text: JAPANESE INTERMEDIATE CODE: A7424 Effective date: 20190104 |
|
A621 | Written request for application examination |
Free format text: JAPANESE INTERMEDIATE CODE: A621 Effective date: 20200306 |
|
A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20201222 |
|
A977 | Report on retrieval |
Free format text: JAPANESE INTERMEDIATE CODE: A971007 Effective date: 20201225 |
|
A601 | Written request for extension of time |
Free format text: JAPANESE INTERMEDIATE CODE: A601 Effective date: 20210322 |
|
A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20210407 |
|
TRDD | Decision of grant or rejection written | ||
A01 | Written decision to grant a patent or to grant a registration (utility model) |
Free format text: JAPANESE INTERMEDIATE CODE: A01 Effective date: 20210921 |
|
A61 | First payment of annual fees (during grant procedure) |
Free format text: JAPANESE INTERMEDIATE CODE: A61 Effective date: 20211021 |
|
R150 | Certificate of patent or registration of utility model |
Ref document number: 6966465 Country of ref document: JP Free format text: JAPANESE INTERMEDIATE CODE: R150 |