KR20080021601A - 스크래치 내성 폴리올레핀 - Google Patents
스크래치 내성 폴리올레핀 Download PDFInfo
- Publication number
- KR20080021601A KR20080021601A KR1020077026876A KR20077026876A KR20080021601A KR 20080021601 A KR20080021601 A KR 20080021601A KR 1020077026876 A KR1020077026876 A KR 1020077026876A KR 20077026876 A KR20077026876 A KR 20077026876A KR 20080021601 A KR20080021601 A KR 20080021601A
- Authority
- KR
- South Korea
- Prior art keywords
- bis
- triazine
- tetramethyl
- hydroxy
- butyl
- 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.)
- Granted
Links
- 229920000098 polyolefin Polymers 0.000 title claims abstract description 109
- 230000003678 scratch resistant effect Effects 0.000 title description 4
- -1 polypropylene Polymers 0.000 claims abstract description 125
- 150000001412 amines Chemical class 0.000 claims abstract description 59
- 239000000654 additive Substances 0.000 claims abstract description 46
- 229920000089 Cyclic olefin copolymer Polymers 0.000 claims abstract description 39
- 239000004743 Polypropylene Substances 0.000 claims abstract description 33
- 229920001155 polypropylene Polymers 0.000 claims abstract description 32
- 235000014113 dietary fatty acids Nutrition 0.000 claims abstract description 24
- 239000000194 fatty acid Substances 0.000 claims abstract description 24
- 229930195729 fatty acid Natural products 0.000 claims abstract description 24
- 150000004665 fatty acids Chemical group 0.000 claims abstract description 24
- 239000007795 chemical reaction product Substances 0.000 claims abstract description 23
- 229920002397 thermoplastic olefin Polymers 0.000 claims abstract description 23
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 claims abstract description 22
- 239000012445 acidic reagent Substances 0.000 claims abstract description 21
- 239000004698 Polyethylene Substances 0.000 claims abstract description 17
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims abstract description 17
- 239000004611 light stabiliser Substances 0.000 claims abstract description 16
- 229920000573 polyethylene Polymers 0.000 claims abstract description 15
- 239000000758 substrate Substances 0.000 claims abstract description 15
- 239000000047 product Substances 0.000 claims abstract description 13
- FUSNPOOETKRESL-ZPHPHTNESA-N (z)-n-octadecyldocos-13-enamide Chemical compound CCCCCCCCCCCCCCCCCCNC(=O)CCCCCCCCCCC\C=C/CCCCCCCC FUSNPOOETKRESL-ZPHPHTNESA-N 0.000 claims abstract description 7
- VMRGZRVLZQSNHC-ZCXUNETKSA-N n-[(z)-octadec-9-enyl]hexadecanamide Chemical compound CCCCCCCCCCCCCCCC(=O)NCCCCCCCC\C=C/CCCCCCCC VMRGZRVLZQSNHC-ZCXUNETKSA-N 0.000 claims abstract description 5
- 239000000203 mixture Substances 0.000 claims description 94
- 229910052757 nitrogen Inorganic materials 0.000 claims description 34
- 230000000996 additive effect Effects 0.000 claims description 19
- 239000003381 stabilizer Substances 0.000 claims description 18
- 150000001875 compounds Chemical class 0.000 claims description 17
- 125000004122 cyclic group Chemical group 0.000 claims description 17
- 238000000034 method Methods 0.000 claims description 15
- UKJARPDLRWBRAX-UHFFFAOYSA-N n,n'-bis(2,2,6,6-tetramethylpiperidin-4-yl)hexane-1,6-diamine Chemical compound C1C(C)(C)NC(C)(C)CC1NCCCCCCNC1CC(C)(C)NC(C)(C)C1 UKJARPDLRWBRAX-UHFFFAOYSA-N 0.000 claims description 12
- 150000007934 α,β-unsaturated carboxylic acids Chemical class 0.000 claims description 12
- 239000007859 condensation product Substances 0.000 claims description 11
- 125000006309 butyl amino group Chemical group 0.000 claims description 10
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 9
- 150000003918 triazines Chemical class 0.000 claims description 9
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims description 8
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 claims description 8
- JYEUMXHLPRZUAT-UHFFFAOYSA-N 1,2,3-triazine Chemical compound C1=CN=NN=C1 JYEUMXHLPRZUAT-UHFFFAOYSA-N 0.000 claims description 7
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 claims description 7
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims description 7
- VVISQEKWYPFFLK-UHFFFAOYSA-N 2-n,2-n,4-n,4-n-tetrabutyl-6-chloro-1,3,5-triazine-2,4-diamine Chemical compound CCCCN(CCCC)C1=NC(Cl)=NC(N(CCCC)CCCC)=N1 VVISQEKWYPFFLK-UHFFFAOYSA-N 0.000 claims description 6
- KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 claims description 6
- XITRBUPOXXBIJN-UHFFFAOYSA-N bis(2,2,6,6-tetramethylpiperidin-4-yl) decanedioate Chemical compound C1C(C)(C)NC(C)(C)CC1OC(=O)CCCCCCCCC(=O)OC1CC(C)(C)NC(C)(C)C1 XITRBUPOXXBIJN-UHFFFAOYSA-N 0.000 claims description 6
- BYZPNECJCZJEFV-UHFFFAOYSA-N 4,6-dichloro-n-[4-(2,2,6,6-tetramethylpiperidin-4-yl)butyl]-1,3,5-triazin-2-amine Chemical compound C1C(C)(C)NC(C)(C)CC1CCCCNC1=NC(Cl)=NC(Cl)=N1 BYZPNECJCZJEFV-UHFFFAOYSA-N 0.000 claims description 5
- STEYNUVPFMIUOY-UHFFFAOYSA-N 4-Hydroxy-1-(2-hydroxyethyl)-2,2,6,6-tetramethylpiperidine Chemical compound CC1(C)CC(O)CC(C)(C)N1CCO STEYNUVPFMIUOY-UHFFFAOYSA-N 0.000 claims description 5
- YZXTWMQYSSMUFH-UHFFFAOYSA-N 4-[6-(1-amino-2,2,6,6-tetramethylpiperidin-4-yl)hexyl]-2,2,6,6-tetramethylpiperidin-1-amine Chemical compound C1C(C)(C)N(N)C(C)(C)CC1CCCCCCC1CC(C)(C)N(N)C(C)(C)C1 YZXTWMQYSSMUFH-UHFFFAOYSA-N 0.000 claims description 5
- KGUHWHHMNQPSRV-UHFFFAOYSA-N [1-(2-hydroxy-2-methylpropoxy)-2,2,6,6-tetramethylpiperidin-4-yl] octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OC1CC(C)(C)N(OCC(C)(C)O)C(C)(C)C1 KGUHWHHMNQPSRV-UHFFFAOYSA-N 0.000 claims description 5
- DVXRGUXKOSSOHV-UHFFFAOYSA-N bis[1-(2-hydroxy-2-methylpropoxy)-2,2,6,6-tetramethylpiperidin-4-yl] decanedioate Chemical compound C1C(C)(C)N(OCC(C)(O)C)C(C)(C)CC1OC(=O)CCCCCCCCC(=O)OC1CC(C)(C)N(OCC(C)(C)O)C(C)(C)C1 DVXRGUXKOSSOHV-UHFFFAOYSA-N 0.000 claims description 5
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 claims description 5
- COFLEVLXIIWATL-UHFFFAOYSA-N n,n'-bis(1,2,2,6,6-pentamethylpiperidin-4-yl)hexane-1,6-diamine Chemical compound C1C(C)(C)N(C)C(C)(C)CC1NCCCCCCNC1CC(C)(C)N(C)C(C)(C)C1 COFLEVLXIIWATL-UHFFFAOYSA-N 0.000 claims description 5
- DARUEKWVLGHJJT-UHFFFAOYSA-N n-butyl-1-[4-[4-(butylamino)-2,2,6,6-tetramethylpiperidin-1-yl]-6-chloro-1,3,5-triazin-2-yl]-2,2,6,6-tetramethylpiperidin-4-amine Chemical compound CC1(C)CC(NCCCC)CC(C)(C)N1C1=NC(Cl)=NC(N2C(CC(CC2(C)C)NCCCC)(C)C)=N1 DARUEKWVLGHJJT-UHFFFAOYSA-N 0.000 claims description 5
- VHSHLMUCYSAUQU-UHFFFAOYSA-N 2-hydroxypropyl methacrylate Chemical compound CC(O)COC(=O)C(C)=C VHSHLMUCYSAUQU-UHFFFAOYSA-N 0.000 claims description 4
- ACZGCWSMSTYWDQ-UHFFFAOYSA-N 3h-1-benzofuran-2-one Chemical compound C1=CC=C2OC(=O)CC2=C1 ACZGCWSMSTYWDQ-UHFFFAOYSA-N 0.000 claims description 4
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 claims description 4
- CMXLJKWFEJEFJE-UHFFFAOYSA-N bis(1,2,2,6,6-pentamethylpiperidin-4-yl) 2-[(4-methoxyphenyl)methylidene]propanedioate Chemical compound C1=CC(OC)=CC=C1C=C(C(=O)OC1CC(C)(C)N(C)C(C)(C)C1)C(=O)OC1CC(C)(C)N(C)C(C)(C)C1 CMXLJKWFEJEFJE-UHFFFAOYSA-N 0.000 claims description 4
- KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 claims description 4
- 125000004915 dibutylamino group Chemical group C(CCC)N(CCCC)* 0.000 claims description 4
- DTSDBGVDESRKKD-UHFFFAOYSA-N n'-(2-aminoethyl)propane-1,3-diamine Chemical compound NCCCNCCN DTSDBGVDESRKKD-UHFFFAOYSA-N 0.000 claims description 4
- 229940116351 sebacate Drugs 0.000 claims description 4
- CXMXRPHRNRROMY-UHFFFAOYSA-L sebacate(2-) Chemical compound [O-]C(=O)CCCCCCCCC([O-])=O CXMXRPHRNRROMY-UHFFFAOYSA-L 0.000 claims description 4
- RXFCIXRFAJRBSG-UHFFFAOYSA-N 3,2,3-tetramine Chemical compound NCCCNCCNCCCN RXFCIXRFAJRBSG-UHFFFAOYSA-N 0.000 claims description 3
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims description 3
- NLMFVJSIGDIJBB-UHFFFAOYSA-N bis(2,2,6,6-tetramethyl-1-octoxypiperidin-3-yl) decanedioate Chemical compound CC1(C)N(OCCCCCCCC)C(C)(C)CCC1OC(=O)CCCCCCCCC(=O)OC1C(C)(C)N(OCCCCCCCC)C(C)(C)CC1 NLMFVJSIGDIJBB-UHFFFAOYSA-N 0.000 claims description 3
- KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical class [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 claims description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 3
- 229910052698 phosphorus Inorganic materials 0.000 claims description 3
- 239000011574 phosphorus Substances 0.000 claims description 3
- OUBISKKOUYNDML-UHFFFAOYSA-N (2,2,6,6-tetramethylpiperidin-4-yl) 2-[bis[2-oxo-2-(2,2,6,6-tetramethylpiperidin-4-yl)oxyethyl]amino]acetate Chemical compound C1C(C)(C)NC(C)(C)CC1OC(=O)CN(CC(=O)OC1CC(C)(C)NC(C)(C)C1)CC(=O)OC1CC(C)(C)NC(C)(C)C1 OUBISKKOUYNDML-UHFFFAOYSA-N 0.000 claims description 2
- CGXOAAMIQPDTPE-UHFFFAOYSA-N 1,2,2,6,6-pentamethylpiperidin-4-amine Chemical compound CN1C(C)(C)CC(N)CC1(C)C CGXOAAMIQPDTPE-UHFFFAOYSA-N 0.000 claims description 2
- FYQOHJWNKFULEZ-UHFFFAOYSA-N 1-(2-hydroxy-2-methylpropoxy)-2,2,6,6-tetramethylpiperidin-4-ol Chemical compound CC(C)(O)CON1C(C)(C)CC(O)CC1(C)C FYQOHJWNKFULEZ-UHFFFAOYSA-N 0.000 claims description 2
- FUVBNYKKKZSBCG-UHFFFAOYSA-N 1-(2-hydroxy-2-methylpropoxy)-2,2,6,6-tetramethylpiperidin-4-one Chemical compound CC(C)(O)CON1C(C)(C)CC(=O)CC1(C)C FUVBNYKKKZSBCG-UHFFFAOYSA-N 0.000 claims description 2
- WICJDHJYOIJBDM-UHFFFAOYSA-N 1-[4-[butyl-[4-[butyl-[1-(2-hydroxy-2-methylpropoxy)-2,2,6,6-tetramethylpiperidin-4-yl]amino]-6-(2-hydroxyethylamino)-1,3,5-triazin-2-yl]amino]-2,2,6,6-tetramethylpiperidin-1-yl]oxy-2-methylpropan-2-ol Chemical compound N=1C(NCCO)=NC(N(CCCC)C2CC(C)(C)N(OCC(C)(C)O)C(C)(C)C2)=NC=1N(CCCC)C1CC(C)(C)N(OCC(C)(C)O)C(C)(C)C1 WICJDHJYOIJBDM-UHFFFAOYSA-N 0.000 claims description 2
- OKELZJLBUAZSCL-UHFFFAOYSA-N 1-cyclohexyloxy-2,2,6,6-tetramethyl-n-octadecylpiperidin-4-amine Chemical compound CC1(C)CC(NCCCCCCCCCCCCCCCCCC)CC(C)(C)N1OC1CCCCC1 OKELZJLBUAZSCL-UHFFFAOYSA-N 0.000 claims description 2
- RKMGAJGJIURJSJ-UHFFFAOYSA-N 2,2,6,6-Tetramethylpiperidine Substances CC1(C)CCCC(C)(C)N1 RKMGAJGJIURJSJ-UHFFFAOYSA-N 0.000 claims description 2
- BWJKLDGAAPQXGO-UHFFFAOYSA-N 2,2,6,6-tetramethyl-4-octadecoxypiperidine Chemical compound CCCCCCCCCCCCCCCCCCOC1CC(C)(C)NC(C)(C)C1 BWJKLDGAAPQXGO-UHFFFAOYSA-N 0.000 claims description 2
- FTVFPPFZRRKJIH-UHFFFAOYSA-N 2,2,6,6-tetramethylpiperidin-4-amine Chemical compound CC1(C)CC(N)CC(C)(C)N1 FTVFPPFZRRKJIH-UHFFFAOYSA-N 0.000 claims description 2
- GVLRGMSHUKNBDP-UHFFFAOYSA-N 2-(1,3,5-triazin-2-ylamino)ethanol Chemical compound OCCNC1=NC=NC=N1 GVLRGMSHUKNBDP-UHFFFAOYSA-N 0.000 claims description 2
- IXAKLSFFPBJWBS-UHFFFAOYSA-N 2-cycloundecyl-7,7,9,9-tetramethyl-1-oxa-3,8-diazaspiro[4.5]decan-4-one Chemical compound C1C(C)(C)NC(C)(C)CC21C(=O)NC(C1CCCCCCCCCC1)O2 IXAKLSFFPBJWBS-UHFFFAOYSA-N 0.000 claims description 2
- GUCMKIKYKIHUTM-UHFFFAOYSA-N 3,3,5,5-tetramethyl-1-[2-(3,3,5,5-tetramethyl-2-oxopiperazin-1-yl)ethyl]piperazin-2-one Chemical compound O=C1C(C)(C)NC(C)(C)CN1CCN1C(=O)C(C)(C)NC(C)(C)C1 GUCMKIKYKIHUTM-UHFFFAOYSA-N 0.000 claims description 2
- SAEZGDDJKSBNPT-UHFFFAOYSA-N 3-dodecyl-1-(1,2,2,6,6-pentamethylpiperidin-4-yl)pyrrolidine-2,5-dione Chemical compound O=C1C(CCCCCCCCCCCC)CC(=O)N1C1CC(C)(C)N(C)C(C)(C)C1 SAEZGDDJKSBNPT-UHFFFAOYSA-N 0.000 claims description 2
- FBIXXCXCZOZFCO-UHFFFAOYSA-N 3-dodecyl-1-(2,2,6,6-tetramethylpiperidin-4-yl)pyrrolidine-2,5-dione Chemical compound O=C1C(CCCCCCCCCCCC)CC(=O)N1C1CC(C)(C)NC(C)(C)C1 FBIXXCXCZOZFCO-UHFFFAOYSA-N 0.000 claims description 2
- QKXSNKQALVWCHY-UHFFFAOYSA-N 4,6-dichloro-n-[4-(1,2,2,6,6-pentamethylpiperidin-4-yl)butyl]-1,3,5-triazin-2-amine Chemical compound C1C(C)(C)N(C)C(C)(C)CC1CCCCNC1=NC(Cl)=NC(Cl)=N1 QKXSNKQALVWCHY-UHFFFAOYSA-N 0.000 claims description 2
- BBPPJRZGZKXRPO-UHFFFAOYSA-N 4,6-dichloro-n-[4-(2,2,6,6-tetramethyl-1-propoxypiperidin-4-yl)butyl]-1,3,5-triazin-2-amine Chemical compound C1C(C)(C)N(OCCC)C(C)(C)CC1CCCCNC1=NC(Cl)=NC(Cl)=N1 BBPPJRZGZKXRPO-UHFFFAOYSA-N 0.000 claims description 2
- IYHCWTYKAWVGPA-UHFFFAOYSA-N 4-[6-(3-amino-1,2,2,6,6-pentamethylpiperidin-4-yl)hexyl]-1,2,2,6,6-pentamethylpiperidin-3-amine Chemical compound NC1C(C)(C)N(C)C(C)(C)CC1CCCCCCC1C(N)C(C)(C)N(C)C(C)(C)C1 IYHCWTYKAWVGPA-UHFFFAOYSA-N 0.000 claims description 2
- DUIYSQWRKVPEOA-UHFFFAOYSA-N 4-[6-(3-amino-2,2,6,6-tetramethyl-1-propoxypiperidin-4-yl)hexyl]-2,2,6,6-tetramethyl-1-propoxypiperidin-3-amine Chemical compound NC1C(C)(C)N(OCCC)C(C)(C)CC1CCCCCCC1C(N)C(C)(C)N(OCCC)C(C)(C)C1 DUIYSQWRKVPEOA-UHFFFAOYSA-N 0.000 claims description 2
- ZCILGMFPJBRCNO-UHFFFAOYSA-N 4-phenyl-2H-benzotriazol-5-ol Chemical compound OC1=CC=C2NN=NC2=C1C1=CC=CC=C1 ZCILGMFPJBRCNO-UHFFFAOYSA-N 0.000 claims description 2
- NJCDRURWJZAMBM-UHFFFAOYSA-N 6-phenyl-1h-1,3,5-triazin-2-one Chemical compound OC1=NC=NC(C=2C=CC=CC=2)=N1 NJCDRURWJZAMBM-UHFFFAOYSA-N 0.000 claims description 2
- IPRLZACALWPEGS-UHFFFAOYSA-N 7,7,9,9-tetramethyl-2-undecyl-1-oxa-3,8-diazaspiro[4.5]decan-4-one Chemical compound O1C(CCCCCCCCCCC)NC(=O)C11CC(C)(C)NC(C)(C)C1 IPRLZACALWPEGS-UHFFFAOYSA-N 0.000 claims description 2
- VPOKLVDHXARWQB-UHFFFAOYSA-N 7,7,9,9-tetramethyl-3-octyl-1,3,8-triazaspiro[4.5]decane-2,4-dione Chemical compound O=C1N(CCCCCCCC)C(=O)NC11CC(C)(C)NC(C)(C)C1 VPOKLVDHXARWQB-UHFFFAOYSA-N 0.000 claims description 2
- RAZWNFJQEZAVOT-UHFFFAOYSA-N 8-acetyl-3-dodecyl-7,7,9,9-tetramethyl-1,3,8-triazaspiro[4.5]decane-2,4-dione Chemical compound O=C1N(CCCCCCCCCCCC)C(=O)NC11CC(C)(C)N(C(C)=O)C(C)(C)C1 RAZWNFJQEZAVOT-UHFFFAOYSA-N 0.000 claims description 2
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 claims description 2
- AVXURJPOCDRRFD-UHFFFAOYSA-N Hydroxylamine Chemical compound ON AVXURJPOCDRRFD-UHFFFAOYSA-N 0.000 claims description 2
- LAGGSSOOLOPEID-UHFFFAOYSA-N N(CC(=O)OCC(CC1CC(N(C(C1)(C)C)N)(C)C)O)(CC(=O)OCC(CC1CC(N(C(C1)(C)C)N)(C)C)O)CC(=O)OCC(CC1CC(N(C(C1)(C)C)N)(C)C)O Chemical compound N(CC(=O)OCC(CC1CC(N(C(C1)(C)C)N)(C)C)O)(CC(=O)OCC(CC1CC(N(C(C1)(C)C)N)(C)C)O)CC(=O)OCC(CC1CC(N(C(C1)(C)C)N)(C)C)O LAGGSSOOLOPEID-UHFFFAOYSA-N 0.000 claims description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims description 2
- RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 claims description 2
- 239000012965 benzophenone Substances 0.000 claims description 2
- FLPKSBDJMLUTEX-UHFFFAOYSA-N bis(1,2,2,6,6-pentamethylpiperidin-4-yl) 2-butyl-2-[(3,5-ditert-butyl-4-hydroxyphenyl)methyl]propanedioate Chemical compound C1C(C)(C)N(C)C(C)(C)CC1OC(=O)C(C(=O)OC1CC(C)(C)N(C)C(C)(C)C1)(CCCC)CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 FLPKSBDJMLUTEX-UHFFFAOYSA-N 0.000 claims description 2
- PVIFXIBJQWPGNU-UHFFFAOYSA-N bis(1-acetyloxy-2,2,6,6-tetramethylpiperidin-4-yl) decanedioate Chemical compound C1C(C)(C)N(OC(=O)C)C(C)(C)CC1OC(=O)CCCCCCCCC(=O)OC1CC(C)(C)N(OC(C)=O)C(C)(C)C1 PVIFXIBJQWPGNU-UHFFFAOYSA-N 0.000 claims description 2
- DLHNOZQXRABONJ-UHFFFAOYSA-N bis(1-cyclohexyloxy-2,2,6,6-tetramethylpiperidin-4-yl) decanedioate Chemical compound CC1(C)CC(OC(=O)CCCCCCCCC(=O)OC2CC(C)(C)N(OC3CCCCC3)C(C)(C)C2)CC(C)(C)N1OC1CCCCC1 DLHNOZQXRABONJ-UHFFFAOYSA-N 0.000 claims description 2
- JLOAPAGFWFMZLD-UHFFFAOYSA-N bis(1-cyclohexyloxy-2,2,6,6-tetramethylpiperidin-4-yl) hexanedioate Chemical compound CC1(C)CC(OC(=O)CCCCC(=O)OC2CC(C)(C)N(OC3CCCCC3)C(C)(C)C2)CC(C)(C)N1OC1CCCCC1 JLOAPAGFWFMZLD-UHFFFAOYSA-N 0.000 claims description 2
- VKVSLLBZHYUYHH-UHFFFAOYSA-N bis(2,2,6,6-tetramethyl-1-octoxypiperidin-3-yl) butanedioate Chemical compound CC1(C)N(OCCCCCCCC)C(C)(C)CCC1OC(=O)CCC(=O)OC1C(C)(C)N(OCCCCCCCC)C(C)(C)CC1 VKVSLLBZHYUYHH-UHFFFAOYSA-N 0.000 claims description 2
- OSIVCXJNIBEGCL-UHFFFAOYSA-N bis(2,2,6,6-tetramethyl-1-octoxypiperidin-4-yl) decanedioate Chemical compound C1C(C)(C)N(OCCCCCCCC)C(C)(C)CC1OC(=O)CCCCCCCCC(=O)OC1CC(C)(C)N(OCCCCCCCC)C(C)(C)C1 OSIVCXJNIBEGCL-UHFFFAOYSA-N 0.000 claims description 2
- WUXGYZUOHKJTEY-UHFFFAOYSA-N bis[1-(2-hydroxy-2-methylpropoxy)-2,2,6,6-tetramethylpiperidin-4-yl] hexanedioate Chemical compound C1C(C)(C)N(OCC(C)(O)C)C(C)(C)CC1OC(=O)CCCCC(=O)OC1CC(C)(C)N(OCC(C)(C)O)C(C)(C)C1 WUXGYZUOHKJTEY-UHFFFAOYSA-N 0.000 claims description 2
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Classifications
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- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
- C08L23/02—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
-
- C—CHEMISTRY; METALLURGY
- 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
- C08F255/00—Macromolecular compounds obtained by polymerising monomers on to polymers of hydrocarbons as defined in group C08F10/00
- C08F255/02—Macromolecular compounds obtained by polymerising monomers on to polymers of hydrocarbons as defined in group C08F10/00 on to polymers of olefins having two or three carbon atoms
-
- 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
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
- C08K3/20—Oxides; Hydroxides
- C08K3/22—Oxides; Hydroxides of metals
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- 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
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- C08K5/005—Stabilisers against oxidation, heat, light, ozone
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- 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
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- C08K5/0066—Flame-proofing or flame-retarding additives
-
- 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
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- C08K5/09—Carboxylic acids; Metal salts thereof; Anhydrides thereof
- C08K5/098—Metal salts of carboxylic acids
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- 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
- C08K5/10—Esters; Ether-esters
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
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- C08L23/02—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L23/04—Homopolymers or copolymers of ethene
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- C—CHEMISTRY; METALLURGY
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Abstract
Description
Claims (12)
- a) 폴리올레핀 기질 및폴리올레핀 기질의 스크래치 내성 및 광안정성을 향상시키기 위한 유효량의b) 카르복시산 시약 관능화된 올레핀 중합체 또는 공중합체,c) 일급 또는 이급 지방산 아미드 및d) i) 저분자량 입체장애 아민 광안정화제 및 ii) 고분자량 입체장애 아민 광안정화제의 조합물의 첨가제 조합물을 포함하는 폴리올레핀 조성물.
- 제 1항에 있어서, 성분(a)는 폴리프로필렌, 폴리에틸렌 또는 열가소성 폴리올레핀인 조성물.
- 제 1항에 있어서, 성분(b)는 알파, 베타-불포화 카르복시산 시약으로 그라프트된 올레핀 중합체 또는 공중합체인 조성물.
- 제 1항에 있어서, 성분(b)는 아크릴산, 메타크릴산, 메틸 아크릴레이트, 메틸 메타크릴레이트, 2-히드록시프로필 메틸아크릴레이트, 부틸 아크릴레이트 및 말레산 무수물로 구성된 군으로부터 선택되는 알파, 베타-불포화 카르복시산 시약으로 그라프트된 올레핀 중합체 또는 공중합체인 조성물.
- 제 1항에 있어서, 성분(b)는 말레산 무수물로 그라프트된 올레핀 중합체 또는 공중합체인 조성물.
- 제 1항에 있어서, 성분(c)는 스테아릴 에루카미드 또는 올레일 팔미트아미드인 조성물.
- 제 1항에 있어서, 저분자량 입체장애 아민은 200 내지 1000 g/몰의 분자량을 갖고 또 고분자량 입체장애 아민은 1200 내지 10,000 g/mol의 분자량을 갖는 조성물.
- 제 1항에 있어서, 저분자량 입체장애 아민은,1) 1-시클로헥실옥시-2,2,6,6-테트라메틸-4-옥타데실아미노피페리딘,2) 비스(2,2,6,6-테트라메틸피페리딘-4-일) 세바케이트,3) 비스(1-아세톡시-2,2,6,6-테트라메틸피페리딘-4-일) 세바케이트,4) 비스(1,2,2,6,6-펜타메틸-4-일) 세바케이트,5) 비스(1-시클로헥실옥시-2,2,6,6-테트라메틸피페리딘-4-일) 세바케이트,6) 비스(1-옥틸옥시-2,2,6,6-테트라메틸피페리딘-4-일) 세바케이트;7) 비스(1-아실-2,2,6,6-테트라메틸피페리딘-4-일) 세바케이트,8) 비스(1,2,2,6,6-펜타메틸-4-피페리딜) n-부틸-3,5-디-t-부틸-4-히드록 시벤질말로네이트9) 2,4-비스[(1-시클로헥실옥시-2,2,6,6-테트라메틸피페리딘-4-일)부틸아미노]-6-(2-히드록시에틸아미노-s-트리아진,10) 비스(1-시클로헥실옥시-2,2,6,6-테트라메틸피페리딘-4-일) 아디페이트,11) 2,4-비스[(1-시클로헥실옥시-2,2,6,6-피페리딘-4-일)부틸아미노]-6-클로로-s-트리아진,12) 1-(2-히드록시-2-메틸프로폭시)-4-히드록시-2,2,6,6-테트라메틸피페리딘,13) 1-(2-히드록시-2-메틸프로폭시)-4-옥소-2,2,6,6-테트라메틸피페리딘,14) 1-(2-히드록시-2-메틸프로폭시)-4-옥타데카노일옥시-2,2,6,6-테트라메틸피페리딘,15) 비스(1-(2-히드록시-2-메틸프로폭시)-2,2,6,6-테트라메틸피페리딘-4-일) 세바케이트,16) 비스(1-(2-히드록시-2-메틸프로폭시)-2,2,6,6-테트라메틸피페리딘-4-일) 아디페이트,17) 2,4-비스{N-[1-(2-히드록시-2-메틸프로폭시)-2,2,6,6-테트라메틸피페리딘-4-일]-N-부틸-아미노}-6-(2-히드록시에틸아미노)-s-트리아진,18) 4-벤조일-2,2,6,6-테트라메틸피페리딘,19) 디-(1,2,2,6,6-펜타메틸피페리딘-4-일) p-메톡시벤질리덴말로네이트,20) 4-스테아릴옥시-2,2,6,6-테트라메틸피페리딘,21) 비스(1-옥틸옥시-2,2,6,6-테트라메틸피페리딜) 숙시네이트,22) 1,2,2,6,6-펜타메틸-4-아미노피페리딘,23) 2-운데실-7,7,9,9-테트라메틸-1-옥사-3,8-디아자-4-옥소-스피로[4,5]데칸,24) 트리스(2,2,6,6-테트라메틸-4-피페리딜) 니트릴로트리아세테이트, 25) 트리스(2-히드록시-3-(아미노-(2,2,6,6-테트라메틸피페리딘-4-일)프로필) 니트릴로트리아세테이트,26) 테트라키스(2,2,6,6-테트라메틸-4-피페리딜)-1,2,3,4-부탄-테트라카르복실레이트,27) 테트라키스(1,2,2,6,6-펜타메틸-4-피페리딜)-1,2,3,4-부탄-테트라카르복실레이트,28) 1,1'-(1,2-에탄디일)-비스(3,3,5,5-테트라메틸피페라지논),29) 3-n-옥틸-7,7,9,9-테트라메틸-1,3,8-트리아자스피로[4.5]데칸-2,4-디온,30) 8-아세틸-3-도데실-7,7,9,9-테트라메틸-1,3,8-트리아자스피로[4.5]데칸-2,4-디온,31) 3-도데실-1-(2,2,6,6-테트라메틸-4-피페리딜)피롤리딘-2,5-디온,32) 3-도데실-1-(1,2,2,6,6-펜타메틸-4-피페리딜)피롤리딘-2,5-디온 및33) N,N'-비스-포르밀-N,N'-비스(2,2,6,6-테트라메틸-4-피페리딜)헥사메틸렌디아민으로 구성된 군으로부터 선택되고, 또고분자량 입체장애 아민은,34) 2,4-비스[(1-시클로헥실옥시-2,2,6,6-피페리딘-4-일)부틸아미노]-6-클로로-s-트리아진과 N,N'-비스(3-아미노프로필)에틸렌디아민)의 반응생성물,35) 1-(2-히드록시에틸)-2,2,6,6-테트라메틸-4-히드록시피페리딘과 숙신산의 축합물,36) N,N'-비스(2,2,6,6-테트라메틸-4-피페리딜)-헥사메틸렌디아민과 4-t-옥틸아미노-2,6-디클로로-1,3,5-트리아진의 직쇄 또는 고리상 축합물,37) N,N'-비스(2,2,6,6-테트라메틸-4-피페리딜)-헥사메틸렌디아민과 4-시클로헥실아미노-2,6-디클로로-1,3,5-트리아진의 직쇄 또는 고리상 축합물,38) N,N'-비스-(2,2,6,6-테트라메틸-4-피페리딜)-헥사메틸렌디아민과 4-모르폴리노-2,6-디클로로-1,3,5-트리아진의 직쇄 또는 고리상 축합물,39) N,N'-비스-(1,2,2,6,6-펜타메틸-4-피페리딜)-헥사메틸렌디아민과 4-모르폴리노-2,6-디클로로-1,3,5-트리아진의 직쇄 또는 고리상 축합물,40) 2-클로로-4,6-비스(4-n-부틸아미노-2,2,6,6-테트라메틸피페리딜)-1,3,5-트리아진과 1,2-비스(3-아미노프로필아미노)에탄의 축합물,41) 2-클로로-4,6-디-(4-n-부틸아미노-1,2,2,6,6-펜타메틸피페리딜)-1,3,5-트리아진과 1,2-비스-(3-아미노프로필아미노)에탄의 축합물,42) 7,7,9,9-테트라메틸-2-시클로운데실-1-옥사-3,8-디아자-4-옥소-스피로 [4,5]데칸과 에피클로로히드린의 반응생성물,43) 폴리[메틸,(3-옥시-(2,2,6,6-테트라메틸피페리딘-4-일)프로필)] 실옥산, CAS#182635-99-0,44) 말레산 무수물-C18-C22-α-올레핀-공중합체와 2,2,6,6-테트라메틸-4-아미노피페리딘의 반응생성물,45) 4,4'-헥사메틸렌-비스(아미노-2,2,6,6-테트라메틸피페리딘)과 2-클로로-4,6-비스(디부틸아미노)-s-트리아진에 의해 말단-캡핑된 2,4-디클로로-6-[(2,2,6,6-테트라-메틸피페리딘-4-일)부틸아미노]-s-트리아진의 축합 생성물인 올리고머성 화합물,46) 4,4'-헥사메틸렌-비스(아미노-1,2,2,6,6-펜타메틸피페리딘)과 2-클로로-4,6-비스(디부틸아미노)-s-트리아진에 의해 말단-캡핑된 2,4-디클로로-6-[(1,2,2,6,6-펜타메틸피페리딘-4-일)부틸아미노]-s-트리아진의 축합 생성물인 올리고머성 화합물,47) 4,4'-헥사메틸렌-비스(아미노-1-프로폭시-2,2,6,6-테트라메틸피페리딘) 과 2-클로로-4,6-비스(디부틸아미노)-s-트리아진에 의해 말단-캡핑된 2,4-디클로로-6-[(1-프로폭시-2,2,6,6-테트라메틸피페리딘-4-일)부틸아미노]-s-트리아진의 축합 생성물인 올리고머성 화합물,48) 4,4'-헥사메틸렌-비스(아미노-1-아실옥시-2,2,6,6-테트라메틸피페리딘) 과 2-클로로-4,6-비스(디부틸아미노)-s-트리아진에 의해 말단 캡핑된 2,4-디클로로-6-[(1-아실옥시-2,2,6,6-테트라메틸피페리딘-4-일)부틸아미노]-s-트리아진의 축합 생성물인 올리고머성 화합물, 및49) 1,2-비스(3-아미노-프로필아미노)에탄을 염화시아누르와 반응시켜 얻은 생성물을 (2,2,6,6-테트라메틸피페리딘-4-일)부틸아민과 반응시키는 것에 의해 얻은 생성물로 구성된 군으로부터 선택되는 조성물.
- 제 1항에 있어서, 저분자량 입체장애 아민은,2) 비스(2,2,6,6-테트라메틸피페리딘-4-일) 세바케이트,6) 비스(1-옥틸옥시-2,2,6,6-테트라메틸피페리딜) 세바케이트,14) 1-(2-히드록시-2-메틸프로폭시)-4-옥타데카노일옥시-2,2,6,6-테트라메틸피페리딘, 및15) 비스(1-(2-히드록시-2-메틸프로폭시)-2,2,6,6-테트라메틸피페리딘-4-일) 세바케이트로 구성된 군으로부터 선택되고 또고분자량 입체장애 아민은,34) 2,4-비스[(1-시클로헥실옥시-2,2,6,6-피페리딘-4-일)부틸아미노]-6-클로로-s-트리아진과 N,N'-비스(3-아미노프로필)에틸렌디아민)의 반응생성물,35) 1-(2-히드록시에틸)-2,2,6,6-테트라메틸-4-히드록시피페리딘과 숙신산의 축합물,36) N,N'-비스(2,2,6,6-테트라메틸-4-피페리딜)-헥사메틸렌디아민과 4-t-옥틸아미노-2,6-디클로로-1,3,5-트리아진의 직쇄 또는 고리상 축합물,38) N,N'-비스-(2,2,6,6-테트라메틸-4-피페리딜)-헥사메틸렌디아민과 4-모르폴리노-2,6-디클로로-1,3,5-트리아진의 직쇄 또는 고리상 축합물,39) N,N'-비스-(1,2,2,6,6-펜타메틸-4-피페리딜)-헥사메틸렌디아민과 4-모르폴리노-2,6-디클로로-1,3,5-트리아진의 직쇄 또는 고리상 축합물,40) 2-클로로-4,6-비스(4-n-부틸아미노-2,2,6,6-테트라메틸피페리딜)-1,3,5-트리아진과 1,2-비스(3-아미노프로필아미노)에탄의 축합물, 및45) 4,4'-헥사메틸렌-비스(아미노-2,2,6,6-테트라메틸피페리딘)과 2-클로로-4,6-비스(디부틸아미노)-s-트리아진에 의해 말단-캡핑된 2,4-디클로로-6-[(2,2,6,6-테트라-메틸피페리딘-4-일)부틸아미노]-s-트리아진의 축합 생성물인 올리고머성 화합물로 구성된 군으로부터 선택되는 조성물.
- 제 1항에 있어서, 히드록실아민 안정화제, 유기 인 안정화제, 벤조푸라논 안정화제 및 히드록시페닐벤조트리아졸, 히드록시페닐-s-트리아진 또는 벤조페논 자외선 흡수제로 구성된 군으로부터 선택된 1 이상의 첨가제를 더 포함하는 조성물.
- b) 카르복시산 시약 관능화된 올레핀 중합체 또는 공중합체,c) 일급 또는 이급 지방산 아미드 및d) i) 저분자량 입체장애 아민 광안정화제 및 ii) 고분자량 입체장애 아민 광안정화제의 조합물의 조합물 첨가제 유효량을 폴리올레핀 기질에 혼입하는 것을 포함하는, 폴리올레핀 기질에 스크래치 내성 및 광안정성을 제공하는 방법.
- b) 카르복시산 시약 관능화된 올레핀 중합체 또는 공중합체,c) 일급 또는 이급 지방산 아미드 및d) i) 저분자량 입체장애 아민 광안정화제 및 ii) 고분자량 입체장애 아민 광안정화제의 조합물의 조합물 첨가제의 폴리올레핀 기질의 스크래치 내성 및 광안정성을 향상시키는 용도.
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US (1) | US20060276571A1 (ko) |
EP (1) | EP1888686B1 (ko) |
JP (1) | JP5259393B2 (ko) |
KR (1) | KR101351865B1 (ko) |
BR (1) | BRPI0612023A2 (ko) |
CA (1) | CA2610329C (ko) |
DK (1) | DK1888686T3 (ko) |
ES (1) | ES2400726T3 (ko) |
PL (1) | PL1888686T3 (ko) |
TW (1) | TWI504659B (ko) |
WO (1) | WO2006131455A1 (ko) |
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KR20160099342A (ko) * | 2015-02-12 | 2016-08-22 | 주식회사 엘지화학 | 카본블랙 분산액 및 이의 제조 방법 |
KR20180014912A (ko) * | 2016-08-02 | 2018-02-12 | (주)비피케미칼 | 고분자용 복합 기능성 첨가제 및 이의 제조방법 |
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-
2006
- 2006-05-29 DK DK06763330.5T patent/DK1888686T3/da active
- 2006-05-29 WO PCT/EP2006/062672 patent/WO2006131455A1/en not_active Application Discontinuation
- 2006-05-29 CA CA2610329A patent/CA2610329C/en active Active
- 2006-05-29 JP JP2008515182A patent/JP5259393B2/ja active Active
- 2006-05-29 BR BRPI0612023-7A patent/BRPI0612023A2/pt not_active Application Discontinuation
- 2006-05-29 ES ES06763330T patent/ES2400726T3/es active Active
- 2006-05-29 PL PL06763330T patent/PL1888686T3/pl unknown
- 2006-05-29 KR KR1020077026876A patent/KR101351865B1/ko active Active
- 2006-05-29 EP EP06763330A patent/EP1888686B1/en active Active
- 2006-06-05 US US11/446,843 patent/US20060276571A1/en not_active Abandoned
- 2006-06-05 TW TW095119831A patent/TWI504659B/zh active
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR20150063001A (ko) * | 2013-11-29 | 2015-06-08 | 롯데케미칼 주식회사 | 가교화 회전 성형용 폴리에틸렌 수지 조성물 및 이로부터 형성된 수지 성형품 |
KR20160099342A (ko) * | 2015-02-12 | 2016-08-22 | 주식회사 엘지화학 | 카본블랙 분산액 및 이의 제조 방법 |
KR20180014912A (ko) * | 2016-08-02 | 2018-02-12 | (주)비피케미칼 | 고분자용 복합 기능성 첨가제 및 이의 제조방법 |
Also Published As
Publication number | Publication date |
---|---|
TWI504659B (zh) | 2015-10-21 |
PL1888686T3 (pl) | 2013-06-28 |
WO2006131455A1 (en) | 2006-12-14 |
JP5259393B2 (ja) | 2013-08-07 |
CA2610329A1 (en) | 2006-12-14 |
BRPI0612023A2 (pt) | 2010-10-13 |
EP1888686A1 (en) | 2008-02-20 |
EP1888686B1 (en) | 2013-01-23 |
ES2400726T3 (es) | 2013-04-11 |
CA2610329C (en) | 2014-01-21 |
US20060276571A1 (en) | 2006-12-07 |
KR101351865B1 (ko) | 2014-02-17 |
TW200708558A (en) | 2007-03-01 |
DK1888686T3 (da) | 2013-04-29 |
JP2008542512A (ja) | 2008-11-27 |
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