KR20020075922A - 폴리올레핀용 안정화제 혼합물 - Google Patents
폴리올레핀용 안정화제 혼합물 Download PDFInfo
- Publication number
- KR20020075922A KR20020075922A KR1020027010787A KR20027010787A KR20020075922A KR 20020075922 A KR20020075922 A KR 20020075922A KR 1020027010787 A KR1020027010787 A KR 1020027010787A KR 20027010787 A KR20027010787 A KR 20027010787A KR 20020075922 A KR20020075922 A KR 20020075922A
- Authority
- KR
- South Korea
- Prior art keywords
- component
- tert
- butyl
- compound
- tetramethylpiperidin
- Prior art date
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- ZRPOKHXBOZQSOX-UHFFFAOYSA-N n-heptadecyl-n-octadecylhydroxylamine Chemical compound CCCCCCCCCCCCCCCCCCN(O)CCCCCCCCCCCCCCCCC ZRPOKHXBOZQSOX-UHFFFAOYSA-N 0.000 description 1
- 125000003136 n-heptyl 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])* 0.000 description 1
- WGCBLWIBXXQTAW-UHFFFAOYSA-N n-hexadecyl-n-octadecylhydroxylamine Chemical compound CCCCCCCCCCCCCCCCCCN(O)CCCCCCCCCCCCCCCC WGCBLWIBXXQTAW-UHFFFAOYSA-N 0.000 description 1
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- OSFOTMWFXQGWKZ-UHFFFAOYSA-N n-phenyl-4-(2,4,4-trimethylpentan-2-yl)aniline Chemical compound C1=CC(C(C)(C)CC(C)(C)C)=CC=C1NC1=CC=CC=C1 OSFOTMWFXQGWKZ-UHFFFAOYSA-N 0.000 description 1
- CVVFFUKULYKOJR-UHFFFAOYSA-N n-phenyl-4-propan-2-yloxyaniline Chemical compound C1=CC(OC(C)C)=CC=C1NC1=CC=CC=C1 CVVFFUKULYKOJR-UHFFFAOYSA-N 0.000 description 1
- NYLGUNUDTDWXQE-UHFFFAOYSA-N n-phenyl-n-prop-2-enylaniline Chemical compound C=1C=CC=CC=1N(CC=C)C1=CC=CC=C1 NYLGUNUDTDWXQE-UHFFFAOYSA-N 0.000 description 1
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- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 1
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- 125000001400 nonyl group Chemical group [H]C([*])([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])[H] 0.000 description 1
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
- JFNLZVQOOSMTJK-KNVOCYPGSA-N norbornene Chemical compound C1[C@@H]2CC[C@H]1C=C2 JFNLZVQOOSMTJK-KNVOCYPGSA-N 0.000 description 1
- 239000002667 nucleating agent Substances 0.000 description 1
- 125000003261 o-tolyl group Chemical group [H]C1=C([H])C(*)=C(C([H])=C1[H])C([H])([H])[H] 0.000 description 1
- IXVLEAZXSJJKFR-UHFFFAOYSA-N octadecyl 2-[(4-hydroxy-3,5-dimethylphenyl)methylsulfanyl]acetate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)CSCC1=CC(C)=C(O)C(C)=C1 IXVLEAZXSJJKFR-UHFFFAOYSA-N 0.000 description 1
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- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
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- 125000004430 oxygen atom Chemical group O* 0.000 description 1
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- XRBCRPZXSCBRTK-UHFFFAOYSA-N phosphonous acid Chemical class OPO XRBCRPZXSCBRTK-UHFFFAOYSA-N 0.000 description 1
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- MQOCIYICOGDBSG-UHFFFAOYSA-M potassium;hexadecanoate Chemical compound [K+].CCCCCCCCCCCCCCCC([O-])=O MQOCIYICOGDBSG-UHFFFAOYSA-M 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
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- 125000006233 propoxy propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])OC([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000005767 propoxymethyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])[#8]C([H])([H])* 0.000 description 1
- 238000010526 radical polymerization reaction Methods 0.000 description 1
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- 150000004760 silicates Chemical class 0.000 description 1
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- 125000004469 siloxy group Chemical group [SiH3]O* 0.000 description 1
- WXMKPNITSTVMEF-UHFFFAOYSA-M sodium benzoate Chemical compound [Na+].[O-]C(=O)C1=CC=CC=C1 WXMKPNITSTVMEF-UHFFFAOYSA-M 0.000 description 1
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- 229940074404 sodium succinate Drugs 0.000 description 1
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- 229940114926 stearate Drugs 0.000 description 1
- 125000003696 stearoyl group Chemical group O=C([*])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])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- KZNICNPSHKQLFF-UHFFFAOYSA-N succinimide Chemical group O=C1CCC(=O)N1 KZNICNPSHKQLFF-UHFFFAOYSA-N 0.000 description 1
- 125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 description 1
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- KKEYFWRCBNTPAC-UHFFFAOYSA-L terephthalate(2-) Chemical compound [O-]C(=O)C1=CC=C(C([O-])=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-L 0.000 description 1
- 150000000000 tetracarboxylic acids Chemical class 0.000 description 1
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- 238000005809 transesterification reaction Methods 0.000 description 1
- 150000003918 triazines Chemical class 0.000 description 1
- 150000003628 tricarboxylic acids Chemical class 0.000 description 1
- 239000013638 trimer Substances 0.000 description 1
- XFNJVJPLKCPIBV-UHFFFAOYSA-N trimethylenediamine Chemical compound NCCCN XFNJVJPLKCPIBV-UHFFFAOYSA-N 0.000 description 1
- CNUJLMSKURPSHE-UHFFFAOYSA-N trioctadecyl phosphite Chemical compound CCCCCCCCCCCCCCCCCCOP(OCCCCCCCCCCCCCCCCCC)OCCCCCCCCCCCCCCCCCC CNUJLMSKURPSHE-UHFFFAOYSA-N 0.000 description 1
- PKYCTRXXOZUHFK-UHFFFAOYSA-N tris(1,2,2,6,6-pentamethylpiperidin-4-yl) phosphite Chemical compound C1C(C)(C)N(C)C(C)(C)CC1OP(OC1CC(C)(C)N(C)C(C)(C)C1)OC1CC(C)(C)N(C)C(C)(C)C1 PKYCTRXXOZUHFK-UHFFFAOYSA-N 0.000 description 1
- TZCXWPBSZLCVFR-UHFFFAOYSA-N tris(2,2,6,6-tetramethyl-1-propylpiperidin-4-yl) phosphate Chemical compound C1C(C)(C)N(CCC)C(C)(C)CC1OP(=O)(OC1CC(C)(C)N(CCC)C(C)(C)C1)OC1CC(C)(C)N(CCC)C(C)(C)C1 TZCXWPBSZLCVFR-UHFFFAOYSA-N 0.000 description 1
- GPRWRDWHHCQROU-UHFFFAOYSA-N tris(2,2,6,6-tetramethyl-1-propylpiperidin-4-yl) phosphite Chemical compound C1C(C)(C)N(CCC)C(C)(C)CC1OP(OC1CC(C)(C)N(CCC)C(C)(C)C1)OC1CC(C)(C)N(CCC)C(C)(C)C1 GPRWRDWHHCQROU-UHFFFAOYSA-N 0.000 description 1
- 229920001862 ultra low molecular weight polyethylene Polymers 0.000 description 1
- 125000002948 undecyl group Chemical group [H]C([*])([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])[H] 0.000 description 1
- 229920001866 very low density polyethylene Polymers 0.000 description 1
- 235000019154 vitamin C Nutrition 0.000 description 1
- 239000011718 vitamin C Substances 0.000 description 1
- 235000019165 vitamin E Nutrition 0.000 description 1
- 239000011709 vitamin E Substances 0.000 description 1
- 229940046009 vitamin E Drugs 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 150000003751 zinc Chemical class 0.000 description 1
- BOXSVZNGTQTENJ-UHFFFAOYSA-L zinc dibutyldithiocarbamate Chemical compound [Zn+2].CCCCN(C([S-])=S)CCCC.CCCCN(C([S-])=S)CCCC BOXSVZNGTQTENJ-UHFFFAOYSA-L 0.000 description 1
- SRWMQSFFRFWREA-UHFFFAOYSA-M zinc formate Chemical compound [Zn+2].[O-]C=O SRWMQSFFRFWREA-UHFFFAOYSA-M 0.000 description 1
- XOOUIPVCVHRTMJ-UHFFFAOYSA-L zinc stearate Chemical compound [Zn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O XOOUIPVCVHRTMJ-UHFFFAOYSA-L 0.000 description 1
- UYPNGYWOKLGXGM-UHFFFAOYSA-L zinc;n-butylcarbamodithioate Chemical compound [Zn+2].CCCCNC([S-])=S.CCCCNC([S-])=S UYPNGYWOKLGXGM-UHFFFAOYSA-L 0.000 description 1
- 150000007934 α,β-unsaturated carboxylic acids Chemical class 0.000 description 1
- 235000004835 α-tocopherol Nutrition 0.000 description 1
- 239000002076 α-tocopherol Substances 0.000 description 1
- 239000011590 β-tocopherol Substances 0.000 description 1
- 235000007680 β-tocopherol Nutrition 0.000 description 1
- 239000002478 γ-tocopherol Substances 0.000 description 1
- QUEDXNHFTDJVIY-UHFFFAOYSA-N γ-tocopherol Chemical class OC1=C(C)C(C)=C2OC(CCCC(C)CCCC(C)CCCC(C)C)(C)CCC2=C1 QUEDXNHFTDJVIY-UHFFFAOYSA-N 0.000 description 1
- QUEDXNHFTDJVIY-DQCZWYHMSA-N γ-tocopherol Chemical compound OC1=C(C)C(C)=C2O[C@@](CCC[C@H](C)CCC[C@H](C)CCCC(C)C)(C)CCC2=C1 QUEDXNHFTDJVIY-DQCZWYHMSA-N 0.000 description 1
- 239000002446 δ-tocopherol Substances 0.000 description 1
Classifications
-
- 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
- C08K5/16—Nitrogen-containing compounds
- C08K5/34—Heterocyclic compounds having nitrogen in the ring
-
- 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
- C08K5/16—Nitrogen-containing compounds
- C08K5/34—Heterocyclic compounds having nitrogen in the ring
- C08K5/3412—Heterocyclic compounds having nitrogen in the ring having one nitrogen atom in the ring
- C08K5/3432—Six-membered rings
- C08K5/3435—Piperidines
-
- 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
- C08K5/0008—Organic ingredients according to more than one of the "one dot" groups of C08K5/01 - C08K5/59
- C08K5/005—Stabilisers against oxidation, heat, light, ozone
-
- 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
- C08K5/16—Nitrogen-containing compounds
- C08K5/34—Heterocyclic compounds having nitrogen in the ring
- C08K5/3442—Heterocyclic compounds having nitrogen in the ring having two nitrogen atoms in the ring
- C08K5/3462—Six-membered rings
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Hydrogenated Pyridines (AREA)
- Processes Of Treating Macromolecular Substances (AREA)
Abstract
Description
Claims (22)
- (A) 입체장애 아민 화합물, 및(B) 극성 잔기 함유 중합체를 (A): (B) 중량비 20:1 내지 1:20으로 함유하고,단, (1) 성분(B)는 성분(A)와 다르고 또 하기 화학식(I) 또는 (II)의 기를 함유하지 않으며, 또(2) 성분(B)는 산성 수소 원자를 갖는 중합체와 다른 것을 특징으로 하는 안정화제 혼합물:(I)(II)상기 식중에서,G는 수소 또는 메틸이고, 또G1및 G2는 서로 독립적으로 수소, 메틸이거나 합쳐져서 치환기 =O 임.
- 제1항에 있어서, 성분(A)가 하나 이상의 하기 화학식(I) 또는 (II)의 기를 함유하는 안정화제 혼합물:(I)(II)상기 식중에서,G는 수소 또는 메틸이고, 또G1및 G2는 서로 독립적으로 수소, 메틸이거나 합쳐져서 치환기 =O 임.
- 제1항에 있어서, 성분(A)가 하기에 나타낸 화합물(5), (13), (14), (23), (24), (36-a-1), (36-a-2), (36-b-1), (36-b-2), (36-d), (49-a-1), (49-a-2), (49-c), (49-d), (49-e), (63), (65), (69-a), (81), (82), (102), (105) 또는 (106)의 화합물에 해당하는 안정화제 혼합물:5) 4-스테아로일옥시-2,2,6,6-테트라메틸피페리딘13) 디(2,2,6,6-테트라메틸피페리딘-4-일)세바케이트14) 디(1,2,2,6,6-펜타메틸피페리딘-4-일)세바케이트23) 디(1,2,2,6,6-펜타메틸피페리딘-4-일)부틸(3,5-디-삼차부틸-4-히드록시벤질)말로네이트24) 디(1-옥틸옥시-2,2,6,6-테트라메틸피페리딘-4-일)세바케이트36-a-1) 1,2,3,4-테트라키스[2,2,6,6-테트라메틸피페리딘-4-일옥시카르보닐]부탄36-a-2) 비스[2,2,6,6-테트라메틸피페리딘-4-일옥시카르보닐]-비스[트리데실옥시카르보닐]부탄36-b-1) 1,2,3,4-테트라키스[1,2,2,6,6-펜타메틸피페리딘-4-일옥시카르보닐]부탄36-b-2) 비스[1,2,2,6,6-펜타메틸피페리딘-4-일옥시카르보닐]-비스[트리데실옥시카르보닐]부탄36-d)49-a-1)49-a-2)49-c) 2-(2,2,6,6-테트라메틸피페리딘-4-일아미노)-2-(2,2,6,6-테트라메틸피페리딘-4-일아미노카르보닐)프로판49-d) 1,6-비스[N-(2,2,6,6-테트라메틸피페리딘-4-일)포르밀아미노]헥산49-e)63) 2,2,4,4-테트라메틸-7-옥사-3,20-디아자-21-옥소디스피로[5.1.11.2]헨아이코산65) 8-아세틸-3-도데실-1,3,8-트리아자-7,7,9,9-테트라메틸스피로[4.5]데칸-2,4-디온69-a)
- 제1항에 있어서, 성분(A)가 하기 화합물(76), (82-a), (84-1-a), (84-1-b), (84-2), (91-1), (92), (93), (96-I), (96-II), (97-I), (97-II), (99-I), (99-II), (99-III), (100-A) 또는 (101-I)의 화합물에 상응하는 안정화제 혼합물:(식중, m4는 2 내지 40의 수임)(식중, m4는 2 내지 40의 수임)(식중, m4는 2 내지 40의 수임)(상기 식중에서, m11 *는 m11에서 정의한 바와 같고, 라디칼 R*는 독립적으로 에틸 또는 2,2,6,6-테트라메틸피페리딘-4-일이며, 단 라디칼 R*중의 50% 이상은 2,2,6,6-테트라메틸피페리딘-4-일이고 나머지 라디칼 R*는 에틸임)(식중, m12는 2 내지 40의 수임)(식중, m12는 2 내지 40의 수임)(식중, m16은 2 내지 50의 수임)(식중, m16 *은 2 내지 50의 수임)(식중, m17은 1 내지 20의 수임)(식중, m17은 1 내지 20의 수임)(식중, G11은 수소 또는 메틸이고 또 m19는 1 내지 25의 수임)(식중, G11은 수소 또는 메틸이고 또 m19는 1 내지 25의 수임)(식중, G11은 수소 또는 메틸이고 또 m19는 1 내지 25의 수임)100-A) 하기 화학식(100a)의 폴리아민을 염화시아누르와 반응시켜 수득한 중간체 생성물을 하기 화학식(100b)의 화합물과 반응시키는 것에 의해 얻을 수 있는 생성물:(식중, m21은 1 내지 20의 수임)
- 제3항에 있어서, 성분(A)가 화합물(5), (13), (14), (24), (49-a-1), (49-a-2) 또는 (49-d)의 화합물에 상응하는 안정화제 혼합물.
- 제3항에 있어서, 성분(A)가 화합물(13)에 상응하는 안정화제 혼합물.
- 제4항에 있어서, 성분(A)가 화합물(76), (84-1-a), (84-1-b), (92), (93), (99-I), (100-A) 또는 (101-I)에 상응하는 안정화제 혼합물.
- 제4항에 있어서, 성분(A)가 화합물(76), (84-1-a), (84-1-b), (92) 또는 (100-A)에 상응하는 안정화제 혼합물.
- 제1항에 있어서, 성분(A): (B)의 중량비가 5:1 내지 1:5인 안정화제 혼합물.
- 제1항에 있어서, 극성 잔기를 함유하는 중합체가,(B-1) 할로겐-함유 중합체,(B-2) α,β-불포화 산으로부터 유도된 중합체 또는 그의 유도체,(B-3) 아크릴로니트릴/부타디엔 공중합체, 아크릴로니트릴/알킬 아크릴레이트 공중합체, 에틸렌/아크릴레이트 공중합체, 아크릴로니트릴/알콕시알킬 아크릴레이트 또는 아크릴로니트릴/비닐 할라이드 공중합체 또는 아크릴로니트릴/알킬 메타크릴레이트/부타디엔 삼중합체,(B-4) 불포화 알코올 및 아민으로부터 유도된 중합체 또는 그의 아실 유도체 또는 아세탈,(B-5) 시클릭 에테르의 동종중합체 또는 공중합체,(B-6) 폴리아세탈,(B-7) 폴리페닐렌 옥사이드, 또는 폴리페닐렌 옥사이드와 다른 중합체의 혼합물,(B-8) 폴리우레탄,(B-9) 폴리아미드 또는 코폴리아미드,(B-10) 폴리우레아, 폴리이미드, 폴리아미드-이미드, 폴리에테르이미드, 폴리에스테르이미드, 폴리히단토인, 폴리벤즈이미다졸 또는 폴리비닐이미다졸,(B-11) 폴리에스테르,(B-12) 폴리카보네이트 또는 폴리에스테르 카보네이트,(B-13) 폴리술폰, 폴리에테르 술폰 또는 폴리에테르 케톤,(B-14) 알데히드와 페놀, 우레아 또는 멜라민으로부터 유도된 중합체,(B-15) 건조 또는 비건조 알키드 수지,(B-16) 불포화 폴리에스테르 수지,(B-17) 가교성 아크릴 수지,(B-18) 멜라민 수지, 우레아 수지, 이소시아네이트, 이소시아누레이트, 폴리이소시아네이트 또는 에폭시 수지와 가교된 알키드 수지, 폴리에스테르 수지 또는 아크릴레이트 수지,(B-19) 에폭시 수지,(B-20) 셀룰로오스 또는 화학적으로 변성된 그의 상동 유도체,(B-21) 폴리오르가노실옥산,(B-22) 폴리비닐포르말(PVF),(B-23) 폴리(아릴-에테르-에테르-케톤)(PEEK), 또는(B-24) 비닐 방향족 단량체의 공중합체인 안정화제 혼합물.
- 제10항에 있어서, 극성 잔기를 함유하는 중합체가 (B-2), (B-4), (B-6), (B-7), (B-8), (B-9), (B-11), (B-12) 및 (B-13)군으로부터 선택되는 안정화제 혼합물.
- 제1항에 있어서, 성분(B)가 폴리아크릴레이트, 폴리메타크릴레이트(PMA), 폴리메틸 메타크릴레이트(PMMA), 폴리아크릴니트릴(PAN), 폴리비닐 알코올(PVA), 폴리비닐 아세테이트(PVAc), 폴리옥시메틸렌(POM), 폴리페닐렌 에테르(PPE), 폴리우레탄, 폴리아미드 3(PA3), 폴리아미드 6(PA6), 폴리아미드 11(PA 11), 폴리아미드 12(PA 12), 폴리아미드 66 (PA 66), 폴리에틸렌 테레프탈레이트(PET), 폴리부틸렌 테레프탈레이트 (PBT), 폴리아세트산(PLA), 폴리카보네이트(PC) 또는 폴리에테르 술폰(PES) 또는 화학식의 반복 단위를 갖는 방향족 지방족 폴리술폰(PSP)인 안정화제 혼합물.
- 제1항에 있어서, 성분(B)가 폴리아미드(PA), 아크릴 에스테르/스티렌/아크릴로니트릴 공중합체(ASA), 스티렌/아크릴로니트릴 공중합체 (SAN), 스티렌/말레산 무수물 공중합체(SMA) 또는 폴리에테르 아미드인 안정화제 혼합물.
- 제1항에 있어서, 성분(B)가 폴리메타크릴레이트(PMA), 폴리메틸 메타크릴레이트 (PMMA), 폴리아미드(PA), 폴리옥시메틸렌(POM), 아크릴 에스테르/스티렌/아크릴로니트릴 공중합체(ASA) 또는 폴리에테르 아미드인 안정화제 혼합물.
- 제1항에 있어서, 성분(A)가 화합물 디(2,2,6,6-테트라메틸피페리딘-4-일)세바케이트이고, 성분(B)가 폴리에틸렌 테레프탈레이트(PET), 폴리아미드 6(PA 6), 폴리카보네이트 (PC), 폴리메타크릴레이트(PMA) 또는 폴리메틸 메타크릴레이트(PMMA), 특히 폴리메틸 메타크릴레이트 (PMMA)이고 성분(A):(B)의 중량비가 5:1 내지 1:5인 안정화제 혼합물.
- 제15항에 있어서, 성분(B)가 폴리메틸 메타크릴레이트 (PMMA)인 안정화제 혼합물.
- 제1항에 있어서, 성분(A)가 화합물 디(2,2,6,6-테트라메틸피페리딘-4-일)세바케이트 또는 화학식의 화합물(식중, m4는 2 내지 40의 수임)이고 또 성분(B)가 폴리아미드(PA), 폴리옥시메틸렌(POM) 또는 폴리에테르 아미드인 안정화제 혼합물.
- 제1항에 있어서, 추가 성분(XX)으로서 Ca의 유기 염, Ca의 무기 염, Ca 산화물 또는 Ca 수산화물을 추가로 함유하는 안정화제 혼합물.
- 제1항에 있어서, 추가의 성분(XXX)으로서 Zn의 유기 염, Zn의 무기염, Zn 산화물, Zn 수산화물, Mg의 유기 염, Mg의 무기 염, Mg 산화물 또는 Mg 수산화물을 추가로 함유하는 안정화제 혼합물.
- 폴리올레핀 및 제1항에 따른 안정화제 혼합물을 포함하는 조성물.
- 제20항에 있어서, 폴리올레핀이 폴리에틸렌 또는 폴리프로필렌 또는 폴리에틸렌 또는 폴리프로필렌의 공중합체인 조성물.
- 폴리올레핀에 제1항에 따른 안정화제 혼합물을 혼입시키는 것을 포함하는 광, 열 또는 산화에 기인한 분해로부터 폴리올레핀을 안정화시키기 위한 방법.
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2001
- 2001-02-15 KR KR1020027010787A patent/KR100727524B1/ko not_active IP Right Cessation
- 2001-02-15 AU AU2001233764A patent/AU2001233764A1/en not_active Abandoned
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- 2001-02-15 RU RU2002123336/04A patent/RU2263688C2/ru not_active IP Right Cessation
- 2001-02-15 AT AT01905773T patent/ATE388988T1/de active
- 2001-02-15 BR BRPI0108512-3A patent/BR0108512B1/pt not_active IP Right Cessation
- 2001-02-15 EP EP01905773A patent/EP1263855B1/en not_active Expired - Lifetime
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Cited By (2)
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KR20170008260A (ko) * | 2014-05-15 | 2017-01-23 | 바스프 에스이 | 고도로 효과적인 안정화제 |
KR20200128053A (ko) * | 2018-02-28 | 2020-11-11 | 사이텍 인더스트리스 인코포레이티드 | 중합체 수지에서의 사용을 위한 과립 안정화제 조성물 및 그의 제조 방법 |
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IN205902B (ko) | 2007-06-29 |
EP1263855A1 (en) | 2002-12-11 |
MXPA02008161A (es) | 2002-11-29 |
CN1404501A (zh) | 2003-03-19 |
CA2400413A1 (en) | 2001-08-30 |
ATE388988T1 (de) | 2008-03-15 |
JP4733898B2 (ja) | 2011-07-27 |
IN2002CH01489A (en) | 2005-01-28 |
RU2002123336A (ru) | 2004-01-20 |
EP1263855B1 (en) | 2008-03-12 |
WO2001062836A1 (en) | 2001-08-30 |
CN100429259C (zh) | 2008-10-29 |
BR0108512B1 (pt) | 2012-07-24 |
US20030069337A1 (en) | 2003-04-10 |
DE60133181D1 (de) | 2008-04-24 |
JP2003524047A (ja) | 2003-08-12 |
KR100727524B1 (ko) | 2007-06-14 |
MX235505B (ko) | 2006-04-05 |
RU2263688C2 (ru) | 2005-11-10 |
DE60133181T2 (de) | 2009-03-12 |
US6869992B2 (en) | 2005-03-22 |
AU2001233764A1 (en) | 2001-09-03 |
CA2400413C (en) | 2010-01-12 |
BR0108512A (pt) | 2002-12-17 |
ES2301528T3 (es) | 2008-07-01 |
PT1263855E (pt) | 2008-04-16 |
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