ZA200401177B - Antioxidants for polyamides. - Google Patents
Antioxidants for polyamides. Download PDFInfo
- Publication number
- ZA200401177B ZA200401177B ZA200401177A ZA200401177A ZA200401177B ZA 200401177 B ZA200401177 B ZA 200401177B ZA 200401177 A ZA200401177 A ZA 200401177A ZA 200401177 A ZA200401177 A ZA 200401177A ZA 200401177 B ZA200401177 B ZA 200401177B
- Authority
- ZA
- South Africa
- Prior art keywords
- polyamide
- polyamides
- antioxidant
- tert
- antioxidants
- Prior art date
Links
- 239000003963 antioxidant agent Substances 0.000 title claims description 26
- 239000004952 Polyamide Substances 0.000 title claims description 24
- 229920002647 polyamide Polymers 0.000 title claims description 24
- 230000003078 antioxidant effect Effects 0.000 claims description 18
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 9
- 239000000203 mixture Substances 0.000 claims description 8
- 229920000642 polymer Polymers 0.000 claims description 3
- 150000001875 compounds Chemical class 0.000 description 8
- 229920002292 Nylon 6 Polymers 0.000 description 6
- ZJIPHXXDPROMEF-UHFFFAOYSA-N dihydroxyphosphanyl dihydrogen phosphite Chemical compound OP(O)OP(O)O ZJIPHXXDPROMEF-UHFFFAOYSA-N 0.000 description 6
- 239000003381 stabilizer Substances 0.000 description 6
- AQSJGOWTSHOLKH-UHFFFAOYSA-N phosphite(3-) Chemical class [O-]P([O-])[O-] AQSJGOWTSHOLKH-UHFFFAOYSA-N 0.000 description 5
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 4
- IWDCLRJOBJJRNH-UHFFFAOYSA-N p-cresol Chemical compound CC1=CC=C(O)C=C1 IWDCLRJOBJJRNH-UHFFFAOYSA-N 0.000 description 4
- 239000004033 plastic Substances 0.000 description 4
- 229920003023 plastic Polymers 0.000 description 4
- -1 polytetramethylene Polymers 0.000 description 4
- OKOBUGCCXMIKDM-UHFFFAOYSA-N Irganox 1098 Chemical group CC(C)(C)C1=C(O)C(C(C)(C)C)=CC(CCC(=O)NCCCCCCNC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)=C1 OKOBUGCCXMIKDM-UHFFFAOYSA-N 0.000 description 3
- 239000007795 chemical reaction product Substances 0.000 description 3
- 238000000354 decomposition reaction Methods 0.000 description 3
- 150000002989 phenols Chemical class 0.000 description 3
- 230000006641 stabilisation Effects 0.000 description 3
- QSRJVOOOWGXUDY-UHFFFAOYSA-N 2-[2-[2-[3-(3-tert-butyl-4-hydroxy-5-methylphenyl)propanoyloxy]ethoxy]ethoxy]ethyl 3-(3-tert-butyl-4-hydroxy-5-methylphenyl)propanoate Chemical compound CC(C)(C)C1=C(O)C(C)=CC(CCC(=O)OCCOCCOCCOC(=O)CCC=2C=C(C(O)=C(C)C=2)C(C)(C)C)=C1 QSRJVOOOWGXUDY-UHFFFAOYSA-N 0.000 description 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
- 229920001007 Nylon 4 Polymers 0.000 description 2
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- 150000004985 diamines Chemical class 0.000 description 2
- 229920001971 elastomer Polymers 0.000 description 2
- 239000000806 elastomer Substances 0.000 description 2
- NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 description 2
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 2
- IVSZLXZYQVIEFR-UHFFFAOYSA-N m-xylene Chemical group CC1=CC=CC(C)=C1 IVSZLXZYQVIEFR-UHFFFAOYSA-N 0.000 description 2
- 230000007246 mechanism Effects 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 238000012545 processing Methods 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 239000011265 semifinished product Substances 0.000 description 2
- 230000002195 synergetic effect Effects 0.000 description 2
- 150000007970 thio esters Chemical class 0.000 description 2
- HECLRDQVFMWTQS-RGOKHQFPSA-N 1755-01-7 Chemical compound C1[C@H]2[C@@H]3CC=C[C@@H]3[C@@H]1C=C2 HECLRDQVFMWTQS-RGOKHQFPSA-N 0.000 description 1
- TVWGHFVGFWIHFN-UHFFFAOYSA-N 2-hexadecan-2-yl-4,6-dimethylphenol Chemical compound CCCCCCCCCCCCCCC(C)C1=CC(C)=CC(C)=C1O TVWGHFVGFWIHFN-UHFFFAOYSA-N 0.000 description 1
- YCGKJPVUGMBDDS-UHFFFAOYSA-N 3-(6-azabicyclo[3.1.1]hepta-1(7),2,4-triene-6-carbonyl)benzamide Chemical compound NC(=O)C1=CC=CC(C(=O)N2C=3C=C2C=CC=3)=C1 YCGKJPVUGMBDDS-UHFFFAOYSA-N 0.000 description 1
- PGGROMGHWHXWJL-UHFFFAOYSA-N 4-(azepane-1-carbonyl)benzamide Chemical compound C1=CC(C(=O)N)=CC=C1C(=O)N1CCCCCC1 PGGROMGHWHXWJL-UHFFFAOYSA-N 0.000 description 1
- 239000004604 Blowing Agent Substances 0.000 description 1
- 229920000089 Cyclic olefin copolymer Polymers 0.000 description 1
- 229920002943 EPDM rubber Polymers 0.000 description 1
- 238000005727 Friedel-Crafts reaction Methods 0.000 description 1
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical compound CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 description 1
- 241000054817 Lycaena dione Species 0.000 description 1
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 1
- 244000237986 Melia azadirachta Species 0.000 description 1
- 235000013500 Melia azadirachta Nutrition 0.000 description 1
- 229920000571 Nylon 11 Polymers 0.000 description 1
- 229920000299 Nylon 12 Polymers 0.000 description 1
- 229920000572 Nylon 6/12 Polymers 0.000 description 1
- JKIJEFPNVSHHEI-UHFFFAOYSA-N Phenol, 2,4-bis(1,1-dimethylethyl)-, phosphite (3:1) Chemical compound CC(C)(C)C1=CC(C(C)(C)C)=CC=C1OP(OC=1C(=CC(=CC=1)C(C)(C)C)C(C)(C)C)OC1=CC=C(C(C)(C)C)C=C1C(C)(C)C JKIJEFPNVSHHEI-UHFFFAOYSA-N 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- YZCKVEUIGOORGS-IGMARMGPSA-N Protium Chemical compound [1H] YZCKVEUIGOORGS-IGMARMGPSA-N 0.000 description 1
- DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 description 1
- 239000003490 Thiodipropionic acid Substances 0.000 description 1
- 239000002250 absorbent Substances 0.000 description 1
- 230000002745 absorbent Effects 0.000 description 1
- 229920000122 acrylonitrile butadiene styrene Polymers 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 230000003712 anti-aging effect Effects 0.000 description 1
- 239000002216 antistatic agent Substances 0.000 description 1
- 239000004760 aramid Substances 0.000 description 1
- 229920003235 aromatic polyamide Polymers 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 229920001400 block copolymer Polymers 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 150000001991 dicarboxylic acids Chemical class 0.000 description 1
- 125000003438 dodecyl 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])C([H])([H])C([H])([H])* 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- MHAJPDPJQMAIIY-UHFFFAOYSA-M hydroperoxide group Chemical group [O-]O MHAJPDPJQMAIIY-UHFFFAOYSA-M 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 238000001746 injection moulding Methods 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- 150000004694 iodide salts Chemical class 0.000 description 1
- 229920000554 ionomer Polymers 0.000 description 1
- 150000003951 lactams Chemical class 0.000 description 1
- 239000004611 light stabiliser Substances 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 229910052748 manganese Inorganic materials 0.000 description 1
- 239000011572 manganese Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 239000006078 metal deactivator Substances 0.000 description 1
- 238000013508 migration Methods 0.000 description 1
- 230000005012 migration Effects 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000003607 modifier Substances 0.000 description 1
- 125000001421 myristyl 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])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- SSDSCDGVMJFTEQ-UHFFFAOYSA-N octadecyl 3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)CCC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 SSDSCDGVMJFTEQ-UHFFFAOYSA-N 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 238000006864 oxidative decomposition reaction Methods 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 239000002530 phenolic antioxidant Substances 0.000 description 1
- XRBCRPZXSCBRTK-UHFFFAOYSA-N phosphonous acid Chemical class OPO XRBCRPZXSCBRTK-UHFFFAOYSA-N 0.000 description 1
- 150000003018 phosphorus compounds Chemical class 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 239000002516 radical scavenger Substances 0.000 description 1
- 239000012744 reinforcing agent Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 125000004079 stearyl 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])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
- 238000003860 storage Methods 0.000 description 1
- 229920001897 terpolymer Polymers 0.000 description 1
- NBRKLOOSMBRFMH-UHFFFAOYSA-N tert-butyl chloride Chemical compound CC(C)(C)Cl NBRKLOOSMBRFMH-UHFFFAOYSA-N 0.000 description 1
- 238000002076 thermal analysis method Methods 0.000 description 1
- 238000005979 thermal decomposition reaction Methods 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 229920006345 thermoplastic polyamide Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
- 150000003568 thioethers Chemical class 0.000 description 1
- 125000002889 tridecyl 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])C([H])([H])C([H])([H])[H] 0.000 description 1
- HVLLSGMXQDNUAL-UHFFFAOYSA-N triphenyl phosphite Natural products C=1C=CC=CC=1OP(OC=1C=CC=CC=1)OC1=CC=CC=C1 HVLLSGMXQDNUAL-UHFFFAOYSA-N 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 150000003751 zinc Chemical class 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
- C08K5/04—Oxygen-containing compounds
- C08K5/10—Esters; Ether-esters
- C08K5/101—Esters; Ether-esters of monocarboxylic acids
- C08K5/105—Esters; Ether-esters of monocarboxylic acids with phenols
-
- 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
- C08K5/13—Phenols; Phenolates
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)
- Mobile Radio Communication Systems (AREA)
- Anti-Oxidant Or Stabilizer Compositions (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE10134327A DE10134327A1 (de) | 2001-07-14 | 2001-07-14 | Antioxidantien für Polyamide |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ZA200401177B true ZA200401177B (en) | 2004-10-29 |
Family
ID=7691821
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ZA200401177A ZA200401177B (en) | 2001-07-14 | 2004-02-13 | Antioxidants for polyamides. |
Country Status (21)
| Country | Link |
|---|---|
| US (2) | US7335693B2 (pt) |
| EP (1) | EP1412428B1 (pt) |
| JP (1) | JP2004535504A (pt) |
| KR (1) | KR100831887B1 (pt) |
| CN (1) | CN1250623C (pt) |
| AT (1) | ATE414123T1 (pt) |
| AU (1) | AU2002328874B2 (pt) |
| BR (1) | BR0211147A (pt) |
| CA (1) | CA2454196A1 (pt) |
| DE (2) | DE10134327A1 (pt) |
| DK (1) | DK1412428T3 (pt) |
| ES (1) | ES2318038T3 (pt) |
| HU (1) | HUP0400366A2 (pt) |
| MX (1) | MXPA04000292A (pt) |
| NO (1) | NO330408B1 (pt) |
| PL (1) | PL203810B1 (pt) |
| PT (1) | PT1412428E (pt) |
| RS (1) | RS2204A (pt) |
| RU (1) | RU2307852C9 (pt) |
| WO (1) | WO2003008492A1 (pt) |
| ZA (1) | ZA200401177B (pt) |
Families Citing this family (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7696260B2 (en) * | 2006-03-30 | 2010-04-13 | Dsm Ip Assets B.V. | Cationic compositions and methods of making and using the same |
| US7897552B2 (en) * | 2007-11-30 | 2011-03-01 | Afton Chemical Corporation | Additives and lubricant formulations for improved antioxidant properties |
| US8854733B2 (en) * | 2007-12-28 | 2014-10-07 | Sumitomo Electric Fine Polymer, Inc. | Optical lens |
| DE102008001475A1 (de) * | 2008-04-30 | 2009-11-05 | Evonik Degussa Gmbh | Phenolharz-aufweisende Polymerzusammensetzung |
| DE102008001470B4 (de) * | 2008-04-30 | 2018-01-04 | Evonik Degussa Gmbh | Kontinuierliches Verfahren zur Herstellung eines Reaktivpolymers |
| KR101173215B1 (ko) * | 2009-09-10 | 2012-08-13 | 금호석유화학 주식회사 | 신규한 티오 화합물 및 이의 제조방법 |
| DE102010044050A1 (de) | 2010-11-17 | 2012-05-24 | Evonik Degussa Gmbh | Verfahren zur kontinuierlichen Herstellung eines Prepolymers basierend auf Phenolharzen, Oxazolinen und Epoxiden |
| JP2016084431A (ja) * | 2014-10-28 | 2016-05-19 | 日立化成株式会社 | ポリアミドイミド樹脂系耐熱性樹脂組成物、塗膜、塗膜板及び耐熱性塗料 |
| CN106916432B (zh) * | 2016-09-01 | 2019-07-19 | 艾特国际有限公司 | 用来稳定聚氧化烯烃聚醚多元醇，防止其氧化降解的方法 |
| CN117511197B (zh) * | 2024-01-05 | 2024-04-16 | 山东祥龙新材料股份有限公司 | 一种耐水解可挤出成型的聚酰胺材料及其制备方法与应用 |
Family Cites Families (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5379935A (en) * | 1976-12-24 | 1978-07-14 | Adeka Argus Chem Co Ltd | Stabilized synthetic resin composition |
| US4127490A (en) * | 1977-12-05 | 1978-11-28 | Basf Wyandotte Corporation | Fiber finish compositions |
| JPS56152863A (en) * | 1980-04-28 | 1981-11-26 | Adeka Argus Chem Co Ltd | Synthetic resin composition |
| US4481317A (en) * | 1983-06-07 | 1984-11-06 | Adeka Argus Chemical Co., Ltd. | Hindered bisphenol diphosphonites and stabilized synthetic resin compositions containing the same |
| US4670492A (en) * | 1983-12-01 | 1987-06-02 | Adeka Argus Chemical Co., Ltd. | Cyclic bis and tris phosphites and stabilized synthetic resin compositions |
| JPS61113649A (ja) * | 1984-11-07 | 1986-05-31 | Adeka Argus Chem Co Ltd | 耐光性の改善された高分子材料組成物 |
| US4624679A (en) * | 1985-01-03 | 1986-11-25 | Morton Thiokol, Inc. | Compositions containing antimicorbial agents in combination with stabilizers |
| US4761247A (en) * | 1987-03-06 | 1988-08-02 | Morton Thiokol, Inc. | Phenol-stabilized microbiocidal compositions |
| US5322734A (en) * | 1993-03-22 | 1994-06-21 | Amoco Corporation | Oxidatively-stabilized poly(vinylmethylether) for hot-melt adhesives |
| EP0669367A1 (de) * | 1994-02-24 | 1995-08-30 | Ciba-Geigy Ag | Phenolische Stabilisatormischungen |
| US5670255A (en) * | 1995-01-23 | 1997-09-23 | Ppg Industries, Inc. | Antioxidant compositions for coating substrates, substrates coated with the same and methods for inhibiting the oxidation of such compositions applied to a substrate |
| ES2162210T3 (es) | 1996-06-11 | 2001-12-16 | Atofina | Colas termofusibles a base de copolimeros de etileno/(met)acrilatos de alquilo y de polialfaolefinas y sus utilizaciones. |
| US6001957A (en) * | 1997-12-23 | 1999-12-14 | General Electric Company | Stabilized polyetherimide resin composition |
| DE19946519A1 (de) * | 1999-09-28 | 2001-08-16 | Basf Ag | Verfahren zur kontinuierlichen Herstellung von Stabilisatordispersionen |
| US6353050B1 (en) * | 2000-10-13 | 2002-03-05 | General Electric Co. | Thermoplastic blend comprising poly(arylene ether) and polyamide |
| DE10058135A1 (de) * | 2000-11-22 | 2002-05-23 | Basf Ag | Verfahren zur Herstellung von Additivdispersionen |
| US8337968B2 (en) * | 2002-09-11 | 2012-12-25 | Boston Scientific Scimed, Inc. | Radiation sterilized medical devices comprising radiation sensitive polymers |
| US7390579B2 (en) * | 2003-11-25 | 2008-06-24 | Magnequench, Inc. | Coating formulation and application of organic passivation layer onto iron-based rare earth powders |
-
2001
- 2001-07-14 DE DE10134327A patent/DE10134327A1/de not_active Withdrawn
-
2002
- 2002-07-11 JP JP2003514046A patent/JP2004535504A/ja active Pending
- 2002-07-11 RS YUP-22/04A patent/RS2204A/sr unknown
- 2002-07-11 US US10/483,262 patent/US7335693B2/en not_active Expired - Fee Related
- 2002-07-11 WO PCT/EP2002/007718 patent/WO2003008492A1/de active Application Filing
- 2002-07-11 ES ES02764669T patent/ES2318038T3/es not_active Expired - Lifetime
- 2002-07-11 DK DK02764669T patent/DK1412428T3/da active
- 2002-07-11 CN CNB028141563A patent/CN1250623C/zh not_active Expired - Fee Related
- 2002-07-11 KR KR1020047000543A patent/KR100831887B1/ko not_active IP Right Cessation
- 2002-07-11 MX MXPA04000292A patent/MXPA04000292A/es active IP Right Grant
- 2002-07-11 DE DE50213012T patent/DE50213012D1/de not_active Expired - Lifetime
- 2002-07-11 RU RU2004101639/04A patent/RU2307852C9/ru not_active IP Right Cessation
- 2002-07-11 AU AU2002328874A patent/AU2002328874B2/en not_active Ceased
- 2002-07-11 PL PL365205A patent/PL203810B1/pl not_active IP Right Cessation
- 2002-07-11 PT PT02764669T patent/PT1412428E/pt unknown
- 2002-07-11 BR BR0211147-0A patent/BR0211147A/pt not_active IP Right Cessation
- 2002-07-11 AT AT02764669T patent/ATE414123T1/de active
- 2002-07-11 EP EP02764669A patent/EP1412428B1/de not_active Expired - Lifetime
- 2002-07-11 CA CA002454196A patent/CA2454196A1/en not_active Abandoned
- 2002-07-11 HU HU0400366A patent/HUP0400366A2/hu unknown
-
2004
- 2004-01-13 NO NO20040157A patent/NO330408B1/no not_active IP Right Cessation
- 2004-02-13 ZA ZA200401177A patent/ZA200401177B/en unknown
-
2007
- 2007-10-30 US US11/929,224 patent/US20080119594A1/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| KR20040024584A (ko) | 2004-03-20 |
| EP1412428A1 (de) | 2004-04-28 |
| WO2003008492A1 (de) | 2003-01-30 |
| US20040192821A1 (en) | 2004-09-30 |
| NO330408B1 (no) | 2011-04-04 |
| ES2318038T3 (es) | 2009-05-01 |
| KR100831887B1 (ko) | 2008-05-23 |
| DK1412428T3 (da) | 2009-03-02 |
| AU2002328874B2 (en) | 2007-01-11 |
| CN1250623C (zh) | 2006-04-12 |
| RU2307852C9 (ru) | 2008-07-20 |
| CN1527862A (zh) | 2004-09-08 |
| US20080119594A1 (en) | 2008-05-22 |
| RU2004101639A (ru) | 2005-06-27 |
| ATE414123T1 (de) | 2008-11-15 |
| HUP0400366A2 (en) | 2004-12-28 |
| EP1412428B1 (de) | 2008-11-12 |
| JP2004535504A (ja) | 2004-11-25 |
| US7335693B2 (en) | 2008-02-26 |
| PL365205A1 (en) | 2004-12-27 |
| PL203810B1 (pl) | 2009-11-30 |
| MXPA04000292A (es) | 2004-05-04 |
| CA2454196A1 (en) | 2003-01-30 |
| RU2307852C2 (ru) | 2007-10-10 |
| NO20040157L (no) | 2004-03-11 |
| RS2204A (en) | 2007-02-05 |
| DE50213012D1 (de) | 2008-12-24 |
| DE10134327A1 (de) | 2002-02-28 |
| BR0211147A (pt) | 2004-06-29 |
| PT1412428E (pt) | 2009-02-02 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US20080119594A1 (en) | Antioxidants for polyamides | |
| JP5315238B2 (ja) | 安定剤としての液体ホスフィットブレンド | |
| KR20100133436A (ko) | 재배열 구조, 환형 및 선형 올리고머를 가지며 유동 거동이 개선된 폴리카르보네이트 | |
| KR19980086705A (ko) | 스모크 생성이 적은 올레핀 중합체 조성물 및 이로부터 제조된 섬유 및 필름 | |
| EP0129825A2 (en) | Modified blends of polyphenylene ether resin and a polyamide | |
| KR20070058666A (ko) | 폴리(아릴렌 에터) 조성물 | |
| KR102617932B1 (ko) | 분해방지제 블렌드 | |
| US4739000A (en) | Antioxidant aromatic tetraphosphites | |
| US4724247A (en) | Antioxidant aromatic diphosphites | |
| EP1253169B1 (en) | Degradation inhibitor for resin material, chlorine water-resistant resin composition and method for inhibiting degradation | |
| CN102257051A (zh) | 用于具有改善的耐氯性的水管的聚烯烃组合物 | |
| JP5508290B2 (ja) | 環状オリゴマーを有し、流動性が改良されたポリカーボネート | |
| JPH1036661A (ja) | ポリアミド、ポリエステルおよびポリケトンの安定化 | |
| JP2002060638A (ja) | 有機高分子材料用安定剤および有機高分子材料組成物 | |
| WO1999018154A1 (fr) | Composition stabilisante pour materiaux polymeres organiques contenant des composes 6-hydroxychroman et compositions de materiaux polymeres organiques correspondantes | |
| CA1200038A (en) | Stabilized linear low density polyethylene | |
| KR101066214B1 (ko) | 열가소성 폴리에스테르 엘라스토머 조성물 및 이의 제조방법 | |
| JPH05306255A (ja) | ジフェニル酢酸誘導体 | |
| EP0548293A1 (en) | Thermooxidative stabilization of polyolefins with an oxo-piperazinyl-triazine and a phosphorous acid ester | |
| JP2001310972A (ja) | 酸化窒素ガスによる有機高分子材料の変色抑制剤組成物およびこれを配合してなる有機高分子材料 | |
| JP2000248113A (ja) | スピロクロマン化合物を含有する高分子材料組成物 | |
| JP3501124B2 (ja) | 有機高分子材料用安定剤および有機高分子材料組成物 | |
| JPH08283569A (ja) | ポリアミド樹脂組成物 |