KR100822837B1 - 아크릴계 고분자 비드 및 이를 포함하는 아크릴졸 조성물 - Google Patents
아크릴계 고분자 비드 및 이를 포함하는 아크릴졸 조성물 Download PDFInfo
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- KR100822837B1 KR100822837B1 KR1020060111956A KR20060111956A KR100822837B1 KR 100822837 B1 KR100822837 B1 KR 100822837B1 KR 1020060111956 A KR1020060111956 A KR 1020060111956A KR 20060111956 A KR20060111956 A KR 20060111956A KR 100822837 B1 KR100822837 B1 KR 100822837B1
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- South Korea
- Prior art keywords
- monomer
- acrylic polymer
- weight
- core
- shell
- 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.)
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- 238000000576 coating method Methods 0.000 claims abstract description 31
- 239000011248 coating agent Substances 0.000 claims abstract description 29
- 238000003860 storage Methods 0.000 claims abstract description 26
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims abstract description 18
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- 239000011259 mixed solution Substances 0.000 claims description 14
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- 238000001694 spray drying Methods 0.000 claims description 9
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- 239000000945 filler Substances 0.000 claims description 7
- 238000004519 manufacturing process Methods 0.000 claims description 7
- 239000002318 adhesion promoter Substances 0.000 claims description 6
- 238000006243 chemical reaction Methods 0.000 claims description 6
- 125000004432 carbon atom Chemical group C* 0.000 claims description 5
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- 125000005397 methacrylic acid ester group Chemical group 0.000 claims description 4
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 2
- 239000012792 core layer Substances 0.000 claims description 2
- 125000005396 acrylic acid ester group Chemical group 0.000 claims 1
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- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 8
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- 230000000052 comparative effect Effects 0.000 description 6
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- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 4
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- 229910052757 nitrogen Inorganic materials 0.000 description 4
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- IRIAEXORFWYRCZ-UHFFFAOYSA-N Butylbenzyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCC1=CC=CC=C1 IRIAEXORFWYRCZ-UHFFFAOYSA-N 0.000 description 2
- KCXZNSGUUQJJTR-UHFFFAOYSA-N Di-n-hexyl phthalate Chemical compound CCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCC KCXZNSGUUQJJTR-UHFFFAOYSA-N 0.000 description 2
- MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Natural products CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 description 2
- NIQCNGHVCWTJSM-UHFFFAOYSA-N Dimethyl phthalate Chemical compound COC(=O)C1=CC=CC=C1C(=O)OC NIQCNGHVCWTJSM-UHFFFAOYSA-N 0.000 description 2
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
- WOBHKFSMXKNTIM-UHFFFAOYSA-N Hydroxyethyl methacrylate Chemical compound CC(=C)C(=O)OCCO WOBHKFSMXKNTIM-UHFFFAOYSA-N 0.000 description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 2
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 2
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 2
- 239000004793 Polystyrene Substances 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- ROOXNKNUYICQNP-UHFFFAOYSA-N ammonium persulfate Chemical compound [NH4+].[NH4+].[O-]S(=O)(=O)OOS([O-])(=O)=O ROOXNKNUYICQNP-UHFFFAOYSA-N 0.000 description 2
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 2
- 229910000019 calcium carbonate Inorganic materials 0.000 description 2
- 239000006229 carbon black Substances 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 239000003431 cross linking reagent Substances 0.000 description 2
- DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 description 2
- FLKPEMZONWLCSK-UHFFFAOYSA-N diethyl phthalate Chemical compound CCOC(=O)C1=CC=CC=C1C(=O)OCC FLKPEMZONWLCSK-UHFFFAOYSA-N 0.000 description 2
- 238000004070 electrodeposition Methods 0.000 description 2
- SUPCQIBBMFXVTL-UHFFFAOYSA-N ethyl 2-methylprop-2-enoate Chemical compound CCOC(=O)C(C)=C SUPCQIBBMFXVTL-UHFFFAOYSA-N 0.000 description 2
- 239000004088 foaming agent Substances 0.000 description 2
- 239000012948 isocyanate Substances 0.000 description 2
- 150000002513 isocyanates Chemical class 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- JRKICGRDRMAZLK-UHFFFAOYSA-L persulfate group Chemical group S(=O)(=O)([O-])OOS(=O)(=O)[O-] JRKICGRDRMAZLK-UHFFFAOYSA-L 0.000 description 2
- 239000010452 phosphate Substances 0.000 description 2
- 229920002223 polystyrene Polymers 0.000 description 2
- 239000007921 spray Substances 0.000 description 2
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 2
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 2
- SOSQXPIKTBUEKF-UHFFFAOYSA-N 1,4-dihexoxy-1,4-dioxobutane-2-sulfonic acid Chemical compound CCCCCCOC(=O)CC(S(O)(=O)=O)C(=O)OCCCCCC SOSQXPIKTBUEKF-UHFFFAOYSA-N 0.000 description 1
- HGUFODBRKLSHSI-UHFFFAOYSA-N 2,3,7,8-tetrachloro-dibenzo-p-dioxin Chemical compound O1C2=CC(Cl)=C(Cl)C=C2OC2=C1C=C(Cl)C(Cl)=C2 HGUFODBRKLSHSI-UHFFFAOYSA-N 0.000 description 1
- JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 description 1
- LIAWCKFOFPPVGF-UHFFFAOYSA-N 2-ethyladamantane Chemical compound C1C(C2)CC3CC1C(CC)C2C3 LIAWCKFOFPPVGF-UHFFFAOYSA-N 0.000 description 1
- QTWJRLJHJPIABL-UHFFFAOYSA-N 2-methylphenol;3-methylphenol;4-methylphenol Chemical compound CC1=CC=C(O)C=C1.CC1=CC=CC(O)=C1.CC1=CC=CC=C1O QTWJRLJHJPIABL-UHFFFAOYSA-N 0.000 description 1
- MUZDXNQOSGWMJJ-UHFFFAOYSA-N 2-methylprop-2-enoic acid;prop-2-enoic acid Chemical compound OC(=O)C=C.CC(=C)C(O)=O MUZDXNQOSGWMJJ-UHFFFAOYSA-N 0.000 description 1
- VEORPZCZECFIRK-UHFFFAOYSA-N 3,3',5,5'-tetrabromobisphenol A Chemical compound C=1C(Br)=C(O)C(Br)=CC=1C(C)(C)C1=CC(Br)=C(O)C(Br)=C1 VEORPZCZECFIRK-UHFFFAOYSA-N 0.000 description 1
- ALKCLFLTXBBMMP-UHFFFAOYSA-N 3,7-dimethylocta-1,6-dien-3-yl hexanoate Chemical compound CCCCCC(=O)OC(C)(C=C)CCC=C(C)C ALKCLFLTXBBMMP-UHFFFAOYSA-N 0.000 description 1
- GNSFRPWPOGYVLO-UHFFFAOYSA-N 3-hydroxypropyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCCO GNSFRPWPOGYVLO-UHFFFAOYSA-N 0.000 description 1
- KUXKWCPBFHIJJJ-UHFFFAOYSA-N 6-hydroxy-2-methylhex-2-enoic acid Chemical compound OC(=O)C(C)=CCCCO KUXKWCPBFHIJJJ-UHFFFAOYSA-N 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- 239000004803 Di-2ethylhexylphthalate Substances 0.000 description 1
- ZVFDTKUVRCTHQE-UHFFFAOYSA-N Diisodecyl phthalate Chemical compound CC(C)CCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC(C)C ZVFDTKUVRCTHQE-UHFFFAOYSA-N 0.000 description 1
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 1
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- KYGZCKSPAKDVKC-UHFFFAOYSA-N Oxolinic acid Chemical compound C1=C2N(CC)C=C(C(O)=O)C(=O)C2=CC2=C1OCO2 KYGZCKSPAKDVKC-UHFFFAOYSA-N 0.000 description 1
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- 150000005215 alkyl ethers Chemical class 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
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- BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
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- 239000000981 basic dye Substances 0.000 description 1
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- 230000015572 biosynthetic process Effects 0.000 description 1
- CMCJNODIWQEOAI-UHFFFAOYSA-N bis(2-butoxyethyl)phthalate Chemical compound CCCCOCCOC(=O)C1=CC=CC=C1C(=O)OCCOCCCC CMCJNODIWQEOAI-UHFFFAOYSA-N 0.000 description 1
- RMKYMNRQXYPJHL-UHFFFAOYSA-N bis(2-ethoxyethyl) benzene-1,2-dicarboxylate Chemical compound CCOCCOC(=O)C1=CC=CC=C1C(=O)OCCOCC RMKYMNRQXYPJHL-UHFFFAOYSA-N 0.000 description 1
- HSUIVCLOAAJSRE-UHFFFAOYSA-N bis(2-methoxyethyl) benzene-1,2-dicarboxylate Chemical compound COCCOC(=O)C1=CC=CC=C1C(=O)OCCOC HSUIVCLOAAJSRE-UHFFFAOYSA-N 0.000 description 1
- ZFMQKOWCDKKBIF-UHFFFAOYSA-N bis(3,5-difluorophenyl)phosphane Chemical compound FC1=CC(F)=CC(PC=2C=C(F)C=C(F)C=2)=C1 ZFMQKOWCDKKBIF-UHFFFAOYSA-N 0.000 description 1
- ZCDOYSPFYFSLEW-UHFFFAOYSA-N chromate(2-) Chemical class [O-][Cr]([O-])(=O)=O ZCDOYSPFYFSLEW-UHFFFAOYSA-N 0.000 description 1
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- 239000003085 diluting agent Substances 0.000 description 1
- FBSAITBEAPNWJG-UHFFFAOYSA-N dimethyl phthalate Natural products CC(=O)OC1=CC=CC=C1OC(C)=O FBSAITBEAPNWJG-UHFFFAOYSA-N 0.000 description 1
- 229960001826 dimethylphthalate Drugs 0.000 description 1
- QQVHEQUEHCEAKS-UHFFFAOYSA-N diundecyl benzene-1,2-dicarboxylate Chemical compound CCCCCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCCCCC QQVHEQUEHCEAKS-UHFFFAOYSA-N 0.000 description 1
- MOTZDAYCYVMXPC-UHFFFAOYSA-N dodecyl hydrogen sulfate Chemical compound CCCCCCCCCCCCOS(O)(=O)=O MOTZDAYCYVMXPC-UHFFFAOYSA-N 0.000 description 1
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- CXPOFJRHCFPDRI-UHFFFAOYSA-N dodecylbenzene;sulfuric acid Chemical compound OS(O)(=O)=O.CCCCCCCCCCCCC1=CC=CC=C1 CXPOFJRHCFPDRI-UHFFFAOYSA-N 0.000 description 1
- SYELZBGXAIXKHU-UHFFFAOYSA-N dodecyldimethylamine N-oxide Chemical compound CCCCCCCCCCCC[N+](C)(C)[O-] SYELZBGXAIXKHU-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
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- WNLRTRBMVRJNCN-UHFFFAOYSA-N hexanedioic acid Natural products OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 1
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- 238000005342 ion exchange Methods 0.000 description 1
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- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 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
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
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- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 1
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- 230000002794 monomerizing effect Effects 0.000 description 1
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- YAFOVCNAQTZDQB-UHFFFAOYSA-N octyl diphenyl phosphate Chemical compound C=1C=CC=CC=1OP(=O)(OCCCCCCCC)OC1=CC=CC=C1 YAFOVCNAQTZDQB-UHFFFAOYSA-N 0.000 description 1
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- 230000035515 penetration Effects 0.000 description 1
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- FURYAADUZGZUGQ-UHFFFAOYSA-N phenoxybenzene;sulfuric acid Chemical compound OS(O)(=O)=O.C=1C=CC=CC=1OC1=CC=CC=C1 FURYAADUZGZUGQ-UHFFFAOYSA-N 0.000 description 1
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- 238000004626 scanning electron microscopy Methods 0.000 description 1
- 229910000077 silane Inorganic materials 0.000 description 1
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- APSBXTVYXVQYAB-UHFFFAOYSA-M sodium docusate Chemical group [Na+].CCCCC(CC)COC(=O)CC(S([O-])(=O)=O)C(=O)OCC(CC)CCCC APSBXTVYXVQYAB-UHFFFAOYSA-M 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
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- 229910052623 talc Inorganic materials 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
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- STCOOQWBFONSKY-UHFFFAOYSA-N tributyl phosphate Chemical compound CCCCOP(=O)(OCCCC)OCCCC STCOOQWBFONSKY-UHFFFAOYSA-N 0.000 description 1
- WVLBCYQITXONBZ-UHFFFAOYSA-N trimethyl phosphate Chemical compound COP(=O)(OC)OC WVLBCYQITXONBZ-UHFFFAOYSA-N 0.000 description 1
- XZZNDPSIHUTMOC-UHFFFAOYSA-N triphenyl phosphate Chemical compound C=1C=CC=CC=1OP(OC=1C=CC=CC=1)(=O)OC1=CC=CC=C1 XZZNDPSIHUTMOC-UHFFFAOYSA-N 0.000 description 1
Classifications
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- C08F265/00—Macromolecular compounds obtained by polymerising monomers on to polymers of unsaturated monocarboxylic acids or derivatives thereof as defined in group C08F20/00
- C08F265/04—Macromolecular compounds obtained by polymerising monomers on to polymers of unsaturated monocarboxylic acids or derivatives thereof as defined in group C08F20/00 on to polymers of esters
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- C08F265/00—Macromolecular compounds obtained by polymerising monomers on to polymers of unsaturated monocarboxylic acids or derivatives thereof as defined in group C08F20/00
- C08F265/04—Macromolecular compounds obtained by polymerising monomers on to polymers of unsaturated monocarboxylic acids or derivatives thereof as defined in group C08F20/00 on to polymers of esters
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- C08F285/00—Macromolecular compounds obtained by polymerising monomers on to preformed graft polymers
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- C08L51/00—Compositions of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers
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- C08L51/00—Compositions of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers
- C08L51/003—Compositions of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers grafted on to macromolecular compounds obtained by reactions only involving unsaturated carbon-to-carbon bonds
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- C09D151/00—Coating compositions based on graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Coating compositions based on derivatives of such polymers
- C09D151/003—Coating compositions based on graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Coating compositions based on derivatives of such polymers grafted on to macromolecular compounds obtained by reactions only involving unsaturated carbon-to-carbon bonds
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Abstract
Description
Claims (15)
- 단독 중합체의 유리전이온도(Tg)가 50℃이하인 탄소수 1~8의 알킬기를 가진 아크릴산에스테르, 탄소수 1~4의 알킬기를 가진 메타크릴산에스테르 및 메타크릴산히드록시알킬에스테르 중에서 선택된 1종 이상인 단량체를 50~90중량% 함유하는 코어 형성 단량체의 유화 중합에 의해 형성되는 코어;단독 중합체의 유리전이온도가 50℃이상인 탄소수 1~4의 알킬기를 가진 메타크릴산에스테르 및 메타크릴산히드록시알킬에스테르 중에서 선택되는 1종 이상인 단량체를 60~90중량% 이상 함유하는 쉘 형성 단량체의 유화 중합에 의해 형성되는 쉘; 및상기 코어 형성 단량체 및 상기 쉘 형성 단량체로 이루어진 군으로부터 선택되는 하나 이상의 단량체 및 아크릴산의 유화 중합에 의해 형성되는 최외각층을 포함하는 코어/쉘/최외각층 구조의 아크릴계 고분자 비드.
- 제 1 항에 있어서, 코어/쉘/최외각층의 단량체의 함량비는 50~80:10~30:10~20중량% 인 것을 특징으로 하는 아크릴계 고분자 비드.
- 제 1 항에 있어서, 평균입경은 10∼100㎛인 것을 특징으로 하는 아크릴계 고분자 비드.
- 제 1 항에 있어서, 아크릴산의 함량은 최외각층을 형성하는 단량체를 기준으 로 5~20중량% 인 것을 특징으로 하는 아크릴계 고분자 비드.
- 제 1 항에 있어서, 중량평균분자량(Mw)이 100,000 ~ 2,000,000 g/mol 의 범위내인 것을 특징으로 하는 아크릴계 고분자 비드.
- 삭제
- 삭제
- 반응기에 이온교환수, 단독 중합체의 유리전이온도(Tg)가 50℃이하인 단량체를 50~90중량% 함유하는 코어 형성 단량체 중 5 내지 60중량%에 해당되는 단량체 및 유화제를 첨가하여 승온하고 수용성 개시제를 투입하여 1 내지 4시간 동안 중합시켜 시드를 형성하는 제 1단계; 잔량의 코어를 형성하는 단량체를 적가하고 1-6시간 동안 반응을 더 진행시켜 코어층을 형성하는 제 2단계; 및 단독 중합체의 유리전이온도가 50℃이상인 단량체를 60~90중량% 이상 함유하는 쉘 형성 단량체를 적가하고 2-4시간 동안 반응을 더 진행시켜 쉘층을 형성하는 제 3단계를 포함하는 유화 중합에 의해 아크릴계 고분자 비드를 포함하는 에멀젼을 제조한 다음, 상기 에멀젼을 분무건조하여 아크릴계 고분자 비드를 제조하는 방법에 있어서,상기 3 단계 중합이 완료된 후, 여기에 상기 코어를 형성하는 단량체 및 상기 쉘을 형성하는 단량체로 이루어진 군으로부터 선택되는 하나 이상의 단량체와 아크릴산, 및 유화제를 포함하는 혼합용액을 적가하고 개시제를 가하여 2~4시간 동안 반응을 더 진행시켜 최외각층을 형성하는 제 4단계를 더 포함하는 것을 특징으로 하는 아크릴계 고분자 비드의 제조방법.
- 제 8 항에 있어서, 제 4 단계 중합이 완료된 후 아크릴계 고분자 비드를 포함하는 에멀젼의 평균입경은 0.4~0.7㎛인 것을 특징으로 하는 아크릴계 고분자 비드의 제조방법.
- 제 8 항에 있어서, 아크릴산의 함량은 최외각층을 형성하는 단량체를 기준으 로 5~20중량% 인 것을 특징으로 하는 아크릴계 고분자 비드의 제조방법.
- 삭제
- 제 1 항의 아크릴계 고분자 비드, 충진제, 가소제, 접착증진제, 안료 및 염료를 포함하는 자동차 언더바디 코팅용 아크릴졸 조성물.
- 제 12 항에 있어서, 아크릴계 고분자 비드 100중량부를 기준으로 상기 가소제 100~200중량부, 충진제 110~180중량부, 접착증진제 10~30중량부, 안료 0~10중량부를 포함하는 자동차 언더바디 코팅용 아크릴졸 조성물.
- 제 12 항에 있어서, 브룩필드 점도계 No.7 스핀들을 이용하여 20℃, 20rpm의 조건에서 측정한 초기점도가 30,000∼80,000cps인 것을 특징으로 하는 자동차용 아크릴졸 조성물.
- 제 12 항에 있어서, 40℃, 95% 항온항습기에 14일 간 보관한 후 20℃, 20rpm의 조건에서 브룩필드 점도계 No.7 스핀들을 이용하여 측정한 점도의 증가율이 초기점도 대비 50% 이내인 것을 특징으로 하는 자동차용 아크릴졸 조성물.
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EP (1) | EP1948708B1 (ko) |
JP (1) | JP5145233B2 (ko) |
KR (1) | KR100822837B1 (ko) |
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Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR100994148B1 (ko) | 2010-07-14 | 2010-11-15 | (주)아팩 | 그라비아 인쇄용 양이온성 수성 수지 조성물 및 그의 제조방법 |
Families Citing this family (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1930388A4 (en) * | 2005-08-22 | 2009-08-26 | Nippon Catalytic Chem Ind | EMULSION FOR VIBRATION DAMPER |
CN101268143B (zh) | 2005-09-20 | 2011-09-21 | 日本特殊涂料株式会社 | 减振组合物 |
US8039541B2 (en) * | 2007-01-23 | 2011-10-18 | Mitsubishi Rayon Co., Ltd. | (Meth)acrylic polymer particle, method for producing the same, plastisol composition made from the polymer particle, and article made from the plastisol composition |
KR20090103222A (ko) * | 2008-03-28 | 2009-10-01 | 주식회사 코오롱 | 저장안정성과 도막 밀착성이 우수한 아크릴 졸 조성물 |
JP5339505B2 (ja) * | 2008-09-10 | 2013-11-13 | 三菱レイヨン株式会社 | ラテックスの製造方法、及びアクリルゾル組成物 |
TW201317281A (zh) | 2011-10-20 | 2013-05-01 | Univ Nat Central | 一種核殼結構之次微米顆粒的製備方法 |
KR20140142329A (ko) * | 2012-03-30 | 2014-12-11 | 쓰리엠 이노베이티브 프로퍼티즈 컴파니 | 일 부분, 속-경화성, 수성 접착제 에멀젼 |
CN103275261B (zh) * | 2013-05-13 | 2015-04-29 | 浙江科冠聚合物有限公司 | 一种汽车海绵用软胶乳 |
CN103275263A (zh) * | 2013-05-13 | 2013-09-04 | 浙江科冠聚合物有限公司 | 一种食品包装用超高阻隔胶乳制备方法 |
KR101725892B1 (ko) * | 2014-08-18 | 2017-04-26 | 주식회사 엘지화학 | 세척성이 우수한 아크릴계 에멀젼 점착제 및 이의 제조방법 |
CN116925291A (zh) * | 2015-07-31 | 2023-10-24 | 罗门哈斯公司 | 用于合成单峰丙烯酸珠粒的寡聚物晶种 |
FI128940B (en) * | 2015-09-04 | 2021-03-31 | Kemira Oyj | Core/shell polymer particles as surface sizing agents |
US10988567B2 (en) * | 2016-03-01 | 2021-04-27 | Basf Coatings Gmbh | Aqueous dispersions containing polymerizates produced in multiple stages and coating agent compositions containing same |
JP7208777B2 (ja) * | 2018-11-30 | 2023-01-19 | 中国塗料株式会社 | 塗料組成物 |
CN114174386A (zh) * | 2019-06-03 | 2022-03-11 | 深圳市志海实业股份有限公司 | 具有良好透明度和耐候性的低温抗冲改性剂 |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6235810B1 (en) * | 1997-03-05 | 2001-05-22 | Neste Chemicals Oy | Method for the preparation of hollow polymer particle latex |
KR20010066310A (ko) * | 1999-12-31 | 2001-07-11 | 김충세 | 우수한 내오염성 및 탄성을 갖는 수성도료용 코어-쉘 수지조성물 및 이의 제조방법 |
KR20040010235A (ko) * | 2002-07-23 | 2004-01-31 | 주식회사 코오롱 | 저장안정성과 도막물성이 향상된 자동차용 아크릴 비드,그 제조방법 및 이를 포함하는 아크릴 졸 조성물 |
Family Cites Families (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5237004A (en) * | 1986-11-18 | 1993-08-17 | Rohm And Haas Company | Thermoplastic and thermoset polymer compositions |
US5157084A (en) * | 1990-10-12 | 1992-10-20 | The Dow Chemical Company | Process of making hollow polymer latex particles |
US5221713A (en) * | 1991-10-07 | 1993-06-22 | Rohm And Haas Company | Co-microagglomeration of emulsion polymers (encapsulated core/shell additives for pvc) |
JP3297764B2 (ja) * | 1993-04-22 | 2002-07-02 | 鐘淵化学工業株式会社 | 常温硬化性組成物 |
JP3490769B2 (ja) * | 1994-06-16 | 2004-01-26 | 三菱レイヨン株式会社 | 壁紙用アクリルゾル組成物 |
KR100468600B1 (ko) * | 1996-12-30 | 2005-06-23 | 고려화학 주식회사 | 입자내부에기공을함유한내충격성코어-쉘유화중합체및이의제조방법 |
EP1162217B1 (en) * | 1998-07-01 | 2008-12-24 | Mitsubishi Rayon Co., Ltd. | Fine acrylic polymer particles and plastisol containing the same |
US6894108B1 (en) * | 1999-09-20 | 2005-05-17 | Mitsubishi Rayon Co., Ltd. | Fine polymer particles for plastisol, process for producing the same, and halogen-free plastisol composition and article made with the same |
CA2409483C (en) * | 2000-05-16 | 2009-01-13 | Sunstar Giken Kabushiki Kaisha | Plastisol composition |
RU2184125C1 (ru) * | 2000-11-30 | 2002-06-27 | Институт катализа им. Г.К.Борескова СО РАН | Водная гетерополимерная дисперсия для изготовления покрытий и способ ее получения |
AU2003281534A1 (en) * | 2002-07-23 | 2004-02-09 | Kolon Industries Inc. | Preparation of acrylic polymer sol for coating |
JP4080899B2 (ja) * | 2003-01-17 | 2008-04-23 | 株式会社クラレ | アクリル系重合体粉末、アクリルゾル及び成形物 |
CN100427543C (zh) * | 2003-01-21 | 2008-10-22 | 株式会社可乐丽 | 丙烯酸类聚合物粉末、丙烯酸溶胶以及成形物 |
US7195820B2 (en) * | 2003-12-09 | 2007-03-27 | Arkema Inc. | Core-shell polymers having hydrophilic shells for improved shell coverage and anti-blocking properties |
JP2005239766A (ja) * | 2004-02-24 | 2005-09-08 | Nippon Zeon Co Ltd | 三層構造アクリル重合体粒子、その製造方法、およびプラスチゾル |
-
2006
- 2006-11-14 EP EP06812599A patent/EP1948708B1/en not_active Not-in-force
- 2006-11-14 US US12/093,421 patent/US20080268251A1/en not_active Abandoned
- 2006-11-14 JP JP2008538831A patent/JP5145233B2/ja not_active Expired - Fee Related
- 2006-11-14 KR KR1020060111956A patent/KR100822837B1/ko not_active Expired - Fee Related
- 2006-11-14 CN CN2006800422191A patent/CN101305025B/zh not_active Expired - Fee Related
- 2006-11-14 TW TW095142032A patent/TWI332966B/zh not_active IP Right Cessation
- 2006-11-14 WO PCT/KR2006/004771 patent/WO2007055550A1/en active Application Filing
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6235810B1 (en) * | 1997-03-05 | 2001-05-22 | Neste Chemicals Oy | Method for the preparation of hollow polymer particle latex |
KR20010066310A (ko) * | 1999-12-31 | 2001-07-11 | 김충세 | 우수한 내오염성 및 탄성을 갖는 수성도료용 코어-쉘 수지조성물 및 이의 제조방법 |
KR20040010235A (ko) * | 2002-07-23 | 2004-01-31 | 주식회사 코오롱 | 저장안정성과 도막물성이 향상된 자동차용 아크릴 비드,그 제조방법 및 이를 포함하는 아크릴 졸 조성물 |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR100994148B1 (ko) | 2010-07-14 | 2010-11-15 | (주)아팩 | 그라비아 인쇄용 양이온성 수성 수지 조성물 및 그의 제조방법 |
Also Published As
Publication number | Publication date |
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KR20070051715A (ko) | 2007-05-18 |
TW200728386A (en) | 2007-08-01 |
WO2007055550A1 (en) | 2007-05-18 |
EP1948708A4 (en) | 2010-01-20 |
EP1948708B1 (en) | 2012-10-10 |
TWI332966B (en) | 2010-11-11 |
JP5145233B2 (ja) | 2013-02-13 |
CN101305025A (zh) | 2008-11-12 |
EP1948708A1 (en) | 2008-07-30 |
JP2009513811A (ja) | 2009-04-02 |
CN101305025B (zh) | 2011-03-30 |
US20080268251A1 (en) | 2008-10-30 |
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