TWI482813B - 包含較佳是含二苯甲酮的（甲基）丙烯酸酯聚合物及與彼不同的（甲基）丙烯酸酯聚合物之混合物的水性分散液的組成物，以及該組成物的用途 - Google Patents
包含較佳是含二苯甲酮的（甲基）丙烯酸酯聚合物及與彼不同的（甲基）丙烯酸酯聚合物之混合物的水性分散液的組成物，以及該組成物的用途 Download PDFInfo
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- TWI482813B TWI482813B TW099108190A TW99108190A TWI482813B TW I482813 B TWI482813 B TW I482813B TW 099108190 A TW099108190 A TW 099108190A TW 99108190 A TW99108190 A TW 99108190A TW I482813 B TWI482813 B TW I482813B
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- Prior art keywords
- meth
- composition
- weight
- acrylate
- methyl
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- 239000000203 mixture Substances 0.000 title claims description 89
- 239000006185 dispersion Substances 0.000 title claims description 49
- 229920000058 polyacrylate Polymers 0.000 title claims description 22
- RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 title description 18
- 239000012965 benzophenone Substances 0.000 title 1
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims description 68
- 238000000576 coating method Methods 0.000 claims description 50
- 239000011248 coating agent Substances 0.000 claims description 39
- 239000000178 monomer Substances 0.000 claims description 36
- 150000001875 compounds Chemical class 0.000 claims description 35
- 125000004432 carbon atom Chemical group C* 0.000 claims description 33
- 229920000642 polymer Polymers 0.000 claims description 30
- 239000001257 hydrogen Substances 0.000 claims description 26
- 229910052739 hydrogen Inorganic materials 0.000 claims description 26
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 22
- 229910052760 oxygen Inorganic materials 0.000 claims description 22
- 125000003118 aryl group Chemical group 0.000 claims description 21
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 19
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims description 19
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 18
- 239000001301 oxygen Substances 0.000 claims description 18
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 claims description 15
- 239000000758 substrate Substances 0.000 claims description 15
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 claims description 13
- 239000007787 solid Substances 0.000 claims description 13
- 150000001252 acrylic acid derivatives Chemical class 0.000 claims description 12
- 229910052717 sulfur Inorganic materials 0.000 claims description 12
- 229910052736 halogen Inorganic materials 0.000 claims description 11
- 150000002367 halogens Chemical class 0.000 claims description 11
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical group N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 10
- 125000000623 heterocyclic group Chemical group 0.000 claims description 10
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 9
- 150000002148 esters Chemical class 0.000 claims description 9
- 239000011593 sulfur Substances 0.000 claims description 9
- 239000004567 concrete Substances 0.000 claims description 8
- 229910052500 inorganic mineral Inorganic materials 0.000 claims description 8
- 238000004519 manufacturing process Methods 0.000 claims description 8
- 239000011707 mineral Substances 0.000 claims description 8
- 238000007720 emulsion polymerization reaction Methods 0.000 claims description 7
- 150000002431 hydrogen Chemical class 0.000 claims description 7
- 229910052757 nitrogen Inorganic materials 0.000 claims description 7
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 6
- 238000005470 impregnation Methods 0.000 claims description 2
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- 238000007334 copolymerization reaction Methods 0.000 claims 1
- -1 4-methyldiphenyl ketone Chemical class 0.000 description 96
- ROOXNKNUYICQNP-UHFFFAOYSA-N ammonium persulfate Chemical compound [NH4+].[NH4+].[O-]S(=O)(=O)OOS([O-])(=O)=O ROOXNKNUYICQNP-UHFFFAOYSA-N 0.000 description 32
- 238000006116 polymerization reaction Methods 0.000 description 22
- 238000000034 method Methods 0.000 description 21
- 229920001577 copolymer Polymers 0.000 description 18
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 18
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 17
- 229910001870 ammonium persulfate Inorganic materials 0.000 description 16
- 235000019395 ammonium persulphate Nutrition 0.000 description 16
- 239000002904 solvent Substances 0.000 description 15
- 239000003505 polymerization initiator Substances 0.000 description 14
- 125000000217 alkyl group Chemical group 0.000 description 13
- SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical compound CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 description 12
- 230000008569 process Effects 0.000 description 11
- 230000000052 comparative effect Effects 0.000 description 10
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- OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 description 9
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- 239000012986 chain transfer agent Substances 0.000 description 9
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 8
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- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 8
- 239000002585 base Substances 0.000 description 8
- 238000004132 cross linking Methods 0.000 description 8
- ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 description 8
- 150000003254 radicals Chemical class 0.000 description 8
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 7
- 150000002576 ketones Chemical class 0.000 description 7
- 239000000463 material Substances 0.000 description 7
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- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 6
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 6
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 6
- 239000004305 biphenyl Substances 0.000 description 6
- 235000010290 biphenyl Nutrition 0.000 description 6
- 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 6
- 239000003995 emulsifying agent Substances 0.000 description 6
- 150000002430 hydrocarbons Chemical class 0.000 description 6
- 239000002245 particle Substances 0.000 description 6
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 5
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 5
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 5
- 150000001298 alcohols Chemical class 0.000 description 5
- 238000006243 chemical reaction Methods 0.000 description 5
- 229910052801 chlorine Inorganic materials 0.000 description 5
- 239000000460 chlorine Substances 0.000 description 5
- 229910052731 fluorine Inorganic materials 0.000 description 5
- 239000011737 fluorine Substances 0.000 description 5
- 125000005843 halogen group Chemical group 0.000 description 5
- 150000002978 peroxides Chemical class 0.000 description 5
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 5
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 4
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonium chloride Substances [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 4
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 4
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 4
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- 235000011114 ammonium hydroxide Nutrition 0.000 description 4
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- 125000006267 biphenyl group Chemical group 0.000 description 4
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 4
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- 229920002554 vinyl polymer Polymers 0.000 description 4
- DGVVWUTYPXICAM-UHFFFAOYSA-N β‐Mercaptoethanol Chemical compound OCCS DGVVWUTYPXICAM-UHFFFAOYSA-N 0.000 description 4
- BEQKKZICTDFVMG-UHFFFAOYSA-N 1,2,3,4,6-pentaoxepane-5,7-dione Chemical compound O=C1OOOOC(=O)O1 BEQKKZICTDFVMG-UHFFFAOYSA-N 0.000 description 3
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- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
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- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
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- 239000004820 Pressure-sensitive adhesive Substances 0.000 description 3
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 3
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- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 3
- 125000003545 alkoxy group Chemical group 0.000 description 3
- 125000004104 aryloxy group Chemical group 0.000 description 3
- 229910052799 carbon Inorganic materials 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 125000004122 cyclic group Chemical group 0.000 description 3
- 125000002704 decyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 3
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- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 3
- 229920001519 homopolymer Polymers 0.000 description 3
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- QNLVSEVOEORLBH-UHFFFAOYSA-N 2,5-bis(2-ethylhexylperoxy)-2,5-dimethylhexane Chemical group CCCCC(CC)COOC(C)(C)CCC(C)(C)OOCC(CC)CCCC QNLVSEVOEORLBH-UHFFFAOYSA-N 0.000 description 2
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- GVSZYZPUKJBOJQ-UHFFFAOYSA-N pentyl 2-methylpropaneperoxoate Chemical group CCCCCOOC(=O)C(C)C GVSZYZPUKJBOJQ-UHFFFAOYSA-N 0.000 description 1
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
- 229940097156 peroxyl Drugs 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 239000012071 phase Substances 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 1
- QIWKUEJZZCOPFV-UHFFFAOYSA-N phenyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OC1=CC=CC=C1 QIWKUEJZZCOPFV-UHFFFAOYSA-N 0.000 description 1
- 125000000286 phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 description 1
- XGRBZUSXGVNWMI-UHFFFAOYSA-N phenylmethoxymethyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCOCC1=CC=CC=C1 XGRBZUSXGVNWMI-UHFFFAOYSA-N 0.000 description 1
- VWSUVZVPDQDVRT-UHFFFAOYSA-N phenylperoxybenzene Chemical compound C=1C=CC=CC=1OOC1=CC=CC=C1 VWSUVZVPDQDVRT-UHFFFAOYSA-N 0.000 description 1
- 125000003356 phenylsulfanyl group Chemical group [*]SC1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
- 235000021317 phosphate Nutrition 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- XNGIFLGASWRNHJ-UHFFFAOYSA-L phthalate(2-) Chemical compound [O-]C(=O)C1=CC=CC=C1C([O-])=O XNGIFLGASWRNHJ-UHFFFAOYSA-L 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920001485 poly(butyl acrylate) polymer Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920002857 polybutadiene Polymers 0.000 description 1
- 150000004291 polyenes Chemical class 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 229920001289 polyvinyl ether Polymers 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 125000000714 pyrimidinyl group Chemical group 0.000 description 1
- 125000002294 quinazolinyl group Chemical group N1=C(N=CC2=CC=CC=C12)* 0.000 description 1
- 125000005493 quinolyl group Chemical group 0.000 description 1
- 125000001567 quinoxalinyl group Chemical group N1=C(C=NC2=CC=CC=C12)* 0.000 description 1
- 238000006479 redox reaction Methods 0.000 description 1
- 239000013557 residual solvent Substances 0.000 description 1
- 238000007761 roller coating Methods 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 239000011877 solvent mixture Substances 0.000 description 1
- 125000006850 spacer group Chemical group 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 238000004611 spectroscopical analysis Methods 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 239000001384 succinic acid Substances 0.000 description 1
- 125000004434 sulfur atom Chemical group 0.000 description 1
- 229920003051 synthetic elastomer Polymers 0.000 description 1
- 239000005061 synthetic rubber Substances 0.000 description 1
- GJBRNHKUVLOCEB-UHFFFAOYSA-N tert-butyl benzenecarboperoxoate Chemical compound CC(C)(C)OOC(=O)C1=CC=CC=C1 GJBRNHKUVLOCEB-UHFFFAOYSA-N 0.000 description 1
- 125000001973 tert-pentyl group Chemical group [H]C([H])([H])C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 125000001302 tertiary amino group Chemical group 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 125000001113 thiadiazolyl group Chemical group 0.000 description 1
- 125000000335 thiazolyl group Chemical group 0.000 description 1
- 125000001544 thienyl group Chemical group 0.000 description 1
- 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 1
- LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 description 1
- 238000005809 transesterification reaction Methods 0.000 description 1
- 150000003626 triacylglycerols Chemical class 0.000 description 1
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
- JLGLQAWTXXGVEM-UHFFFAOYSA-N triethylene glycol monomethyl ether Chemical group COCCOCCOCCO JLGLQAWTXXGVEM-UHFFFAOYSA-N 0.000 description 1
- 229940070710 valerate Drugs 0.000 description 1
- NQPDZGIKBAWPEJ-UHFFFAOYSA-N valeric acid Chemical group CCCCC(O)=O NQPDZGIKBAWPEJ-UHFFFAOYSA-N 0.000 description 1
- ZTWTYVWXUKTLCP-UHFFFAOYSA-N vinylphosphonic acid Chemical compound OP(O)(=O)C=C ZTWTYVWXUKTLCP-UHFFFAOYSA-N 0.000 description 1
- NLVXSWCKKBEXTG-UHFFFAOYSA-N vinylsulfonic acid Chemical compound OS(=O)(=O)C=C NLVXSWCKKBEXTG-UHFFFAOYSA-N 0.000 description 1
- 239000012855 volatile organic compound Substances 0.000 description 1
- 230000004580 weight loss Effects 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B41/00—After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone
- C04B41/009—After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone characterised by the material treated
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B41/00—After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone
- C04B41/45—Coating or impregnating, e.g. injection in masonry, partial coating of green or fired ceramics, organic coating compositions for adhering together two concrete elements
- C04B41/46—Coating or impregnating, e.g. injection in masonry, partial coating of green or fired ceramics, organic coating compositions for adhering together two concrete elements with organic materials
- C04B41/48—Macromolecular compounds
- C04B41/483—Polyacrylates
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B41/00—After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone
- C04B41/60—After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone of only artificial stone
- C04B41/61—Coating or impregnation
- C04B41/62—Coating or impregnation with organic materials
- C04B41/63—Macromolecular compounds
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L33/00—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
- C08L33/04—Homopolymers or copolymers of esters
- C08L33/06—Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, which oxygen atoms are present only as part of the carboxyl radical
- C08L33/10—Homopolymers or copolymers of methacrylic acid esters
- C08L33/12—Homopolymers or copolymers of methyl methacrylate
-
- 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
- C09D133/10—Homopolymers or copolymers of methacrylic acid esters
- C09D133/12—Homopolymers or copolymers of methyl methacrylate
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B2111/00—Mortars, concrete or artificial stone or mixtures to prepare them, characterised by specific function, property or use
- C04B2111/60—Flooring materials
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2205/00—Polymer mixtures characterised by other features
- C08L2205/02—Polymer mixtures characterised by other features containing two or more polymers of the same C08L -group
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Ceramic Engineering (AREA)
- Organic Chemistry (AREA)
- Materials Engineering (AREA)
- Structural Engineering (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Life Sciences & Earth Sciences (AREA)
- Wood Science & Technology (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Paints Or Removers (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE102009001776A DE102009001776A1 (de) | 2009-03-24 | 2009-03-24 | Zusammensetzung umfassend als wässrige Dispersion vorzugsweise Benzophenon-haltige (Meth)acrylatpolymere in Mischung mit von diesen verschiedenen (Meth)acrylatpolymeren sowie die Verwendung der Zusammensetzung |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| TW201105730A TW201105730A (en) | 2011-02-16 |
| TWI482813B true TWI482813B (zh) | 2015-05-01 |
Family
ID=42040274
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| TW099108190A TWI482813B (zh) | 2009-03-24 | 2010-03-19 | 包含較佳是含二苯甲酮的（甲基）丙烯酸酯聚合物及與彼不同的（甲基）丙烯酸酯聚合物之混合物的水性分散液的組成物，以及該組成物的用途 |
Country Status (10)
| Country | Link |
|---|---|
| US (1) | US8669328B2 (enExample) |
| EP (1) | EP2411466B1 (enExample) |
| JP (1) | JP5709835B2 (enExample) |
| KR (1) | KR101714094B1 (enExample) |
| CN (1) | CN102369240B (enExample) |
| DE (1) | DE102009001776A1 (enExample) |
| ES (1) | ES2428398T3 (enExample) |
| RU (1) | RU2011142631A (enExample) |
| TW (1) | TWI482813B (enExample) |
| WO (1) | WO2010108762A1 (enExample) |
Families Citing this family (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2012145857A1 (en) * | 2011-04-25 | 2012-11-01 | Evonik Röhm Gmbh | Aqueous dispersion of preferably benzophenone-containing (meth)acrylate polymers for leather coating |
| DE102011088149A1 (de) | 2011-12-09 | 2013-06-13 | Evonik Industries Ag | Beschichteter Verbundkörper, umfassend ein Verbundmaterial |
| EP2878606B1 (en) * | 2013-11-29 | 2015-08-05 | ICAP-SIRA S.p.A. | UV-curable composition and pressure sensitive adhesive having breathability derived therefrom, as well as method for manufacturing the same |
| BR112017012880B1 (pt) * | 2014-12-19 | 2021-12-21 | Dow Global Technologies Llc | Dispersão aquosa de polímero e método de preparação da mesma |
| JP6791615B2 (ja) * | 2015-03-06 | 2020-11-25 | スリーエム イノベイティブ プロパティズ カンパニー | 紫外線架橋性組成物 |
| KR102012695B1 (ko) * | 2016-04-04 | 2019-08-22 | 주식회사 엘지화학 | 광학용 점착 필름 |
| US11512152B2 (en) | 2017-02-27 | 2022-11-29 | Lg Chem, Ltd. | Method of preparing acrylic adhesive and adhesive film prepared therefrom |
| KR102267309B1 (ko) * | 2017-11-30 | 2021-06-18 | (주)엘지하우시스 | 광경화성 점착제 조성물 및 점착 필름 |
| JP7297794B2 (ja) | 2018-05-23 | 2023-06-26 | エボニック オペレーションズ ゲーエムベーハー | ケト官能化芳香族（メタ）アクリレートの製造方法 |
| ES2822120T3 (es) | 2018-07-17 | 2021-04-29 | Evonik Operations Gmbh | Método para preparar (met)acrilatos ácidos de C-H |
| EP3599232A1 (de) | 2018-07-26 | 2020-01-29 | Evonik Operations GmbH | Verfahren zur herstellung von n-methyl(meth)acrylamid |
| US11945967B2 (en) * | 2020-07-02 | 2024-04-02 | Behr Process Corporation | Dirt pick up resistant latex resin |
| CN112002458A (zh) * | 2020-08-03 | 2020-11-27 | 浙江泰仑电力集团有限责任公司 | 无机填料表面包银和其水性光固化导电银浆及其制备方法 |
| EP3981841B1 (de) * | 2020-10-06 | 2024-07-31 | Sika Technology AG | Bodenbelag enthaltend uv-nachweisbare grundierung |
| EP4634244A1 (en) * | 2022-12-16 | 2025-10-22 | Akzo Nobel Coatings International B.V. | Coating composition comprising a binder polymer obtainable by copolymerizing a monomer mixture comprising a vinyl monomer and a butenolide monomer |
| CN116376384B (zh) * | 2023-04-21 | 2024-02-02 | 江苏扬瑞新型材料股份有限公司 | 一种uv-led固化的高性能环保涂料 |
| WO2025042167A1 (ko) * | 2023-08-18 | 2025-02-27 | 주식회사 엘지화학 | 광개시형 공중합 수지, 리튬 이차전지용 가교구조 함유 분리막 및 이의 제조 방법 |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH05170941A (ja) * | 1991-01-24 | 1993-07-09 | Mitsubishi Rayon Co Ltd | 耐候性が改良されたアクリル樹脂フィルム |
| JP2002087870A (ja) * | 2000-07-05 | 2002-03-27 | Rohm & Haas Co | グロスコートされたセメント質基体を提供する方法 |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BE793048A (fr) | 1971-12-23 | 1973-06-20 | Wacker Chemie Gmbh | Procede evitant les phenomenes d'efflorescence sur les dalles de couverture en beton |
| DE2439341A1 (de) | 1974-08-16 | 1976-02-26 | Bayer Ag | Kontinuierliche substanzpolymerisation von vinylderivaten |
| US4511699A (en) | 1982-06-21 | 1985-04-16 | The General Tire & Rubber Company | Flexible thermoplastic vinyl chloride polymers and acrylate terpolymers |
| DE3827975A1 (de) | 1988-08-18 | 1990-03-01 | Basf Ag | Verfahren zur verhinderung von ausblueherscheinungen auf mineralischen substraten |
| FR2697530B1 (fr) | 1992-11-04 | 1994-12-16 | Rhone Poulenc Chimie | Liant pour peinture à base de latex acrylique ou styrène/acrylate. |
| JP3453586B2 (ja) * | 1993-11-04 | 2003-10-06 | 一方社油脂工業株式会社 | 耐光性ラテックス組成物およびラテックスから製造される製品の耐光性改良方法 |
| US5900472A (en) | 1996-12-23 | 1999-05-04 | Sartomer Technology | Copolymerizable benzophenone photoinitiators |
| JP2000109703A (ja) | 1998-10-02 | 2000-04-18 | Jsr Corp | 水系分散体 |
| DE19858851C5 (de) * | 1998-12-19 | 2006-09-28 | Celanese Emulsions Gmbh | Wässrige Copolymerisatdispersion auf Acrylatbasis, Verfahren zu ihrer Herstellung sowie ihre Verwendung in elastischen Beschichtungen |
| ATE285457T1 (de) * | 1999-04-14 | 2005-01-15 | Basf Ag | Verfahren zur verklebung einer uv-durchlässigen folie mit einem weiteren substrat |
| JP2002338934A (ja) | 2001-05-17 | 2002-11-27 | Three M Innovative Properties Co | 接着剤組成物及び接着性物品 |
| EP1371694B1 (en) * | 2002-06-14 | 2010-03-03 | Rohm And Haas Company | Polymeric nanoparticle formulations and their use for improving the dirt pick up resistance of a coating |
| JP5170941B2 (ja) | 2005-01-06 | 2013-03-27 | ダイキン工業株式会社 | ヨウ化水素の製造方法 |
| JP4817675B2 (ja) * | 2005-03-02 | 2011-11-16 | スリーエム イノベイティブ プロパティズ カンパニー | （メタ）アクリル系フィルム、及びそれを用いたマーキングフィルム、レセプターシート |
| DE102005062687A1 (de) * | 2005-12-23 | 2007-07-05 | Röhm Gmbh | PMMA-Folie mit besonders hoher Witterungsbeständigkeit und hoher UV-Schutzwirkung |
| KR101276597B1 (ko) * | 2006-05-11 | 2013-06-20 | 헨켈 아게 운트 코. 카게아아 | 아크릴계 핫멜트 접착제 |
-
2009
- 2009-03-24 DE DE102009001776A patent/DE102009001776A1/de not_active Withdrawn
-
2010
- 2010-03-02 EP EP10705887.7A patent/EP2411466B1/de not_active Not-in-force
- 2010-03-02 CN CN201080011678.XA patent/CN102369240B/zh not_active Expired - Fee Related
- 2010-03-02 RU RU2011142631/04A patent/RU2011142631A/ru not_active Application Discontinuation
- 2010-03-02 JP JP2012501224A patent/JP5709835B2/ja not_active Expired - Fee Related
- 2010-03-02 ES ES10705887T patent/ES2428398T3/es active Active
- 2010-03-02 KR KR1020117022236A patent/KR101714094B1/ko not_active Expired - Fee Related
- 2010-03-02 WO PCT/EP2010/052575 patent/WO2010108762A1/de not_active Ceased
- 2010-03-02 US US13/201,889 patent/US8669328B2/en not_active Expired - Fee Related
- 2010-03-19 TW TW099108190A patent/TWI482813B/zh not_active IP Right Cessation
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH05170941A (ja) * | 1991-01-24 | 1993-07-09 | Mitsubishi Rayon Co Ltd | 耐候性が改良されたアクリル樹脂フィルム |
| JP2002087870A (ja) * | 2000-07-05 | 2002-03-27 | Rohm & Haas Co | グロスコートされたセメント質基体を提供する方法 |
Also Published As
| Publication number | Publication date |
|---|---|
| EP2411466B1 (de) | 2013-07-17 |
| DE102009001776A1 (de) | 2010-09-30 |
| HK1164913A1 (en) | 2012-09-28 |
| WO2010108762A1 (de) | 2010-09-30 |
| KR101714094B1 (ko) | 2017-03-08 |
| JP2012521456A (ja) | 2012-09-13 |
| CN102369240B (zh) | 2014-01-08 |
| ES2428398T3 (es) | 2013-11-07 |
| TW201105730A (en) | 2011-02-16 |
| US20110319514A1 (en) | 2011-12-29 |
| EP2411466A1 (de) | 2012-02-01 |
| US8669328B2 (en) | 2014-03-11 |
| KR20120001733A (ko) | 2012-01-04 |
| JP5709835B2 (ja) | 2015-04-30 |
| CN102369240A (zh) | 2012-03-07 |
| RU2011142631A (ru) | 2013-04-27 |
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