ES2428332T3 - Composiciones de policarbonato modificadas a resistencia elevada a los choques que contienen compuestos de fósforo ácidos con polímero de injerto por emulsión precipitado básicamente - Google Patents
Composiciones de policarbonato modificadas a resistencia elevada a los choques que contienen compuestos de fósforo ácidos con polímero de injerto por emulsión precipitado básicamente Download PDFInfo
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- ES2428332T3 ES2428332T3 ES09763851T ES09763851T ES2428332T3 ES 2428332 T3 ES2428332 T3 ES 2428332T3 ES 09763851 T ES09763851 T ES 09763851T ES 09763851 T ES09763851 T ES 09763851T ES 2428332 T3 ES2428332 T3 ES 2428332T3
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- GUJOJGAPFQRJSV-UHFFFAOYSA-N dialuminum;dioxosilane;oxygen(2-);hydrate Chemical compound O.[O-2].[O-2].[O-2].[Al+3].[Al+3].O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O GUJOJGAPFQRJSV-UHFFFAOYSA-N 0.000 description 1
- 150000001991 dicarboxylic acids Chemical class 0.000 description 1
- 150000001993 dienes Chemical class 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 1
- ROORDVPLFPIABK-UHFFFAOYSA-N diphenyl carbonate Chemical compound C=1C=CC=CC=1OC(=O)OC1=CC=CC=C1 ROORDVPLFPIABK-UHFFFAOYSA-N 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 238000010616 electrical installation Methods 0.000 description 1
- 239000008151 electrolyte solution Substances 0.000 description 1
- 229940021013 electrolyte solution Drugs 0.000 description 1
- 238000004945 emulsification Methods 0.000 description 1
- 125000004185 ester group Chemical group 0.000 description 1
- 125000005670 ethenylalkyl group Chemical group 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000012757 flame retardant agent Substances 0.000 description 1
- 238000010528 free radical solution polymerization reaction Methods 0.000 description 1
- 230000008014 freezing Effects 0.000 description 1
- 238000007710 freezing Methods 0.000 description 1
- 238000004817 gas chromatography Methods 0.000 description 1
- 238000005227 gel permeation chromatography Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 239000003365 glass fiber Substances 0.000 description 1
- 150000002366 halogen compounds Chemical class 0.000 description 1
- 125000005842 heteroatom Chemical group 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- BHEPBYXIRTUNPN-UHFFFAOYSA-N hydridophosphorus(.) (triplet) Chemical compound [PH] BHEPBYXIRTUNPN-UHFFFAOYSA-N 0.000 description 1
- 125000004435 hydrogen atom Chemical class [H]* 0.000 description 1
- 230000003301 hydrolyzing effect Effects 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 239000003999 initiator Substances 0.000 description 1
- 150000002484 inorganic compounds Chemical class 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 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
- 238000004898 kneading Methods 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- WGLQHTKRQPBTRE-UHFFFAOYSA-L magnesium;acetic acid;sulfate Chemical compound [Mg+2].CC(O)=O.[O-]S([O-])(=O)=O WGLQHTKRQPBTRE-UHFFFAOYSA-L 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000012803 melt mixture Substances 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 239000010445 mica Substances 0.000 description 1
- 229910052618 mica group Inorganic materials 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 239000006082 mold release agent Substances 0.000 description 1
- 150000002763 monocarboxylic acids Chemical class 0.000 description 1
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 1
- 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
- 230000003287 optical effect Effects 0.000 description 1
- 150000004028 organic sulfates Chemical class 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- QCDYQQDYXPDABM-UHFFFAOYSA-N phloroglucinol Chemical compound OC1=CC(O)=CC(O)=C1 QCDYQQDYXPDABM-UHFFFAOYSA-N 0.000 description 1
- 150000003016 phosphoric acids Chemical class 0.000 description 1
- 229910052615 phyllosilicate Inorganic materials 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920002285 poly(styrene-co-acrylonitrile) Polymers 0.000 description 1
- 229920001707 polybutylene terephthalate Polymers 0.000 description 1
- 229920006149 polyester-amide block copolymer Polymers 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920000139 polyethylene terephthalate Polymers 0.000 description 1
- 239000005020 polyethylene terephthalate Substances 0.000 description 1
- 239000003505 polymerization initiator Substances 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- USHAGKDGDHPEEY-UHFFFAOYSA-L potassium persulfate Chemical compound [K+].[K+].[O-]S(=O)(=O)OOS([O-])(=O)=O USHAGKDGDHPEEY-UHFFFAOYSA-L 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- XRVCFZPJAHWYTB-UHFFFAOYSA-N prenderol Chemical compound CCC(CC)(CO)CO XRVCFZPJAHWYTB-UHFFFAOYSA-N 0.000 description 1
- 239000003223 protective agent Substances 0.000 description 1
- 239000012966 redox initiator Substances 0.000 description 1
- 230000003014 reinforcing effect Effects 0.000 description 1
- 239000012266 salt solution Substances 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 238000004062 sedimentation Methods 0.000 description 1
- 229920002545 silicone oil Polymers 0.000 description 1
- 229920002379 silicone rubber Polymers 0.000 description 1
- 239000000779 smoke Substances 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 235000017550 sodium carbonate Nutrition 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- 125000001273 sulfonato group Chemical group [O-]S(*)(=O)=O 0.000 description 1
- 238000010557 suspension polymerization reaction Methods 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 235000012222 talc Nutrition 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 238000005809 transesterification reaction Methods 0.000 description 1
- STCOOQWBFONSKY-UHFFFAOYSA-N tributyl phosphate Chemical compound CCCCOP(=O)(OCCCC)OCCCC STCOOQWBFONSKY-UHFFFAOYSA-N 0.000 description 1
- QXJQHYBHAIHNGG-UHFFFAOYSA-N trimethylolethane Chemical compound OCC(C)(CO)CO QXJQHYBHAIHNGG-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
- LIPMRGQQBZJCTM-UHFFFAOYSA-N tris(2-propan-2-ylphenyl) phosphate Chemical compound CC(C)C1=CC=CC=C1OP(=O)(OC=1C(=CC=CC=1)C(C)C)OC1=CC=CC=C1C(C)C LIPMRGQQBZJCTM-UHFFFAOYSA-N 0.000 description 1
- XHGIFBQQEGRTPB-UHFFFAOYSA-N tris(prop-2-enyl) phosphate Chemical compound C=CCOP(=O)(OCC=C)OCC=C XHGIFBQQEGRTPB-UHFFFAOYSA-N 0.000 description 1
- BIKXLKXABVUSMH-UHFFFAOYSA-N trizinc;diborate Chemical compound [Zn+2].[Zn+2].[Zn+2].[O-]B([O-])[O-].[O-]B([O-])[O-] BIKXLKXABVUSMH-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L69/00—Compositions of polycarbonates; Compositions of derivatives of polycarbonates
- C08L69/005—Polyester-carbonates
-
- 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
- C08F2/00—Processes of polymerisation
- C08F2/12—Polymerisation in non-solvents
- C08F2/16—Aqueous medium
- C08F2/22—Emulsion polymerisation
-
- 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
- C08K5/49—Phosphorus-containing compounds
- C08K5/51—Phosphorus bound to oxygen
-
- 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
- C08K5/49—Phosphorus-containing compounds
- C08K5/51—Phosphorus bound to oxygen
- C08K5/52—Phosphorus bound to oxygen only
- C08K5/527—Cyclic esters
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- 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
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- 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
- C08L51/04—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 rubbers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L69/00—Compositions of polycarbonates; Compositions of derivatives of polycarbonates
-
- 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
- C08K5/09—Carboxylic acids; Metal salts thereof; Anhydrides thereof
- C08K5/098—Metal salts of carboxylic acids
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)
- Graft Or Block Polymers (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE102008060536 | 2008-12-04 | ||
| DE102008060536A DE102008060536A1 (de) | 2008-12-04 | 2008-12-04 | Saure Phosphorverbindungen enthaltende schlagzähmodifizierte Polycarbonat-Zusammensetzungen mit basisch gefälltem Emulsionspfropfpolymersiat |
| PCT/EP2009/008299 WO2010063381A1 (de) | 2008-12-04 | 2009-11-21 | Saure phosphorverbindungen enthaltende schlagzähmodifizierte polycarbonat-zusammensetzungen mit basisch gefälltem emulsionspfropfpolymersiat |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES2428332T3 true ES2428332T3 (es) | 2013-11-07 |
Family
ID=41722992
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES09763851T Active ES2428332T3 (es) | 2008-12-04 | 2009-11-21 | Composiciones de policarbonato modificadas a resistencia elevada a los choques que contienen compuestos de fósforo ácidos con polímero de injerto por emulsión precipitado básicamente |
Country Status (12)
| Country | Link |
|---|---|
| US (1) | US7943686B2 (OSRAM) |
| EP (1) | EP2373743B1 (OSRAM) |
| JP (1) | JP5705741B2 (OSRAM) |
| KR (1) | KR101678240B1 (OSRAM) |
| CN (1) | CN102239218B (OSRAM) |
| BR (1) | BRPI0922282A2 (OSRAM) |
| CA (1) | CA2745362C (OSRAM) |
| DE (1) | DE102008060536A1 (OSRAM) |
| ES (1) | ES2428332T3 (OSRAM) |
| MX (1) | MX2011005747A (OSRAM) |
| TW (1) | TWI504672B (OSRAM) |
| WO (1) | WO2010063381A1 (OSRAM) |
Families Citing this family (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2345538B8 (en) * | 2010-01-13 | 2014-07-23 | Armacell Enterprise GmbH & Co. KG | Method for fire protection and modification of properties of expanded polyesters |
| FR2969167B1 (fr) * | 2010-12-15 | 2013-01-11 | Arkema France | Composition thermoplastique modifiee choc amelioree |
| FR2969158B1 (fr) | 2010-12-15 | 2013-01-18 | Arkema France | Procede pour modifiants chocs et composition thermoplastique modifiee choc ayant une resistance hydrolytique amelioree |
| TWI472570B (zh) | 2011-02-15 | 2015-02-11 | Toray Industries | 熱塑性樹脂組成物及其成形品 |
| MX2014004847A (es) | 2011-10-26 | 2014-05-27 | Bayer Ip Gmbh | Procedimiento para la preparacion y estabilizacion de composiciones de policarbonato modificadas al impacto usando disoluciones diluidas de compuestos acidos. |
| BR112014009287A8 (pt) * | 2011-10-26 | 2017-06-20 | Bayer Ip Gmbh | composições de policarbonato estabilizadas com misturas de ácido silícico e um ácido inorgânico |
| EP2840116B1 (en) * | 2012-04-18 | 2019-01-02 | Kaneka Corporation | Rubber graft copolymer, and thermoplastic resin composition containing rubber graft copolymer |
| EP2657259A1 (de) | 2012-04-23 | 2013-10-30 | Bayer MaterialScience AG | ABS-Zusammensetzungen mit verbesserter Oberfläche nach Wärme-Feucht-Lagerung |
| JP6345686B2 (ja) * | 2012-12-07 | 2018-06-20 | コベストロ、ドイチュラント、アクチエンゲゼルシャフトCovestro Deutschland Ag | 難燃性ポリカーボネート成形組成物iv |
| JP6379602B2 (ja) * | 2014-04-04 | 2018-08-29 | 三菱ケミカル株式会社 | ポリカーボネート樹脂用強化剤、ポリカーボネート樹脂組成物及び成形品 |
| WO2017055416A1 (de) | 2015-10-02 | 2017-04-06 | Covestro Deutschland Ag | Polycarbonat-zusammensetzungen mit verbesserter stabilisierung |
| EP3365390B1 (de) | 2015-10-23 | 2020-06-17 | Covestro Deutschland AG | Verfahren zur herstellung von polycarbonat-formmassen mit verbesserter thermischer verarbeitungsstabilität |
| KR102556201B1 (ko) * | 2017-11-13 | 2023-07-14 | 이네오스 스티롤루션 그룹 게엠베하 | 열가소성 성형 조성물 및 개선된 표면 품질을 갖는 이로부터 제조된 물품 |
| FR3078068B1 (fr) | 2018-02-16 | 2020-11-06 | Arkema France | Polymere a couches multiples comprenant un fragment comprenant du phosphore, son procede de preparation, son utilisation et composition comprenant celui-ci |
| JP7475879B2 (ja) * | 2020-02-03 | 2024-04-30 | 日本エイアンドエル株式会社 | 熱可塑性樹脂組成物及びその製造方法 |
Family Cites Families (36)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1495626B1 (de) | 1960-03-30 | 1971-06-09 | Bayer Ag | Verfahren zum herstellen von polyestern |
| US3419634A (en) | 1966-01-03 | 1968-12-31 | Gen Electric | Organopolysiloxane polycarbonate block copolymers |
| FR1580834A (OSRAM) | 1968-01-04 | 1969-09-12 | ||
| DE2232877B2 (de) | 1972-07-05 | 1980-04-10 | Werner & Pfleiderer, 7000 Stuttgart | Verfahren zur Herstellung von Polyestern |
| JPS5039599B2 (OSRAM) | 1973-03-30 | 1975-12-18 | ||
| DE2407776A1 (de) | 1974-02-19 | 1975-09-04 | Licentia Gmbh | Schaltung zur regelung der betriebsspannung fuer die transistor-zeilenendstufe eines fernsehempfaengers |
| JPS5292295A (en) | 1976-01-29 | 1977-08-03 | Sumitomo Chem Co Ltd | Preparation of aromatic polyester |
| IT1116721B (it) | 1976-04-02 | 1986-02-10 | Allied Chem | Copolimero bisfenolo a tereftalato carbonato lavorabili in massa fusa |
| DE2715932A1 (de) | 1977-04-09 | 1978-10-19 | Bayer Ag | Schnellkristallisierende poly(aethylen/alkylen)-terephthalate |
| DE2842005A1 (de) | 1978-09-27 | 1980-04-10 | Bayer Ag | Polycarbonate mit alkylphenyl-endgruppen, ihre herstellung und ihre verwendung |
| JPS5556141A (en) * | 1978-10-23 | 1980-04-24 | Sakai Chem Ind Co Ltd | Thermoplastic resin composition |
| JPS5594930A (en) | 1979-01-10 | 1980-07-18 | Sumitomo Chem Co Ltd | Preparation of aromatic polyester by improved bulk polymerization process |
| DE2929229A1 (de) * | 1979-07-19 | 1981-02-12 | Bayer Ag | Stabilisierte thermoplastische formmassen |
| DE2940024A1 (de) | 1979-10-03 | 1981-04-16 | Bayer Ag, 5090 Leverkusen | Aromatische polyester, verfahren zu ihrer herstellung und ihre verwendung zur herstellung von spritzgussartikeln, folien und ueberzuegen |
| DE3007934A1 (de) | 1980-03-01 | 1981-09-17 | Bayer Ag, 5090 Leverkusen | Aromatische polyestercarbonate, verfahren zu ihrer herstellung und ihre verwendung zur herstellung von spritzgussartikeln, folien und ueberzuegen |
| DE3334782A1 (de) | 1983-04-19 | 1984-10-25 | Bayer Ag, 5090 Leverkusen | Verfahren zur herstellung von polydiorganosiloxanen mit hydroxyaryloxy-endgruppen |
| DE3631539A1 (de) | 1986-09-17 | 1988-03-24 | Bayer Ag | Alterungsbestaendige thermoplastische formmassen mit guter zaehigkeit |
| DE3631540A1 (de) | 1986-09-17 | 1988-03-24 | Bayer Ag | Thermoplastische formmassen mit hoher alterungsbestaendigkeit und guter tieftemperaturzaehigkeit |
| DE3704657A1 (de) | 1987-02-14 | 1988-08-25 | Bayer Ag | Teilchenfoermige mehrphasenpolymerisate |
| DE3704655A1 (de) | 1987-02-14 | 1988-08-25 | Bayer Ag | Teilchenfoermige mehrphasenpolymerisate |
| DE3738143A1 (de) | 1987-11-10 | 1989-05-18 | Bayer Ag | Verwendung von redoxpfropfpolymerisaten zur verbesserung der benzinbestaendigkeit von thermoplastischen, aromatischen polycarbonat- und/oder polyestercarbonat-formmassen |
| DE3832396A1 (de) | 1988-08-12 | 1990-02-15 | Bayer Ag | Dihydroxydiphenylcycloalkane, ihre herstellung und ihre verwendung zur herstellung von hochmolekularen polycarbonaten |
| NL8802346A (nl) | 1988-09-22 | 1990-04-17 | Gen Electric | Polymeermengsel met aromatisch polycarbonaat, styreen bevattend copolymeer en/of entpolymeer en een vlamvertragend middel, daaruit gevormde voorwerpen. |
| DE3913509A1 (de) * | 1989-04-25 | 1990-10-31 | Bayer Ag | Neue emulgatoren und verfahren zur herstellung grobteiliger homodisperser polymerdispersionen unter verwendung dieser emulgatoren |
| DE4221935A1 (de) * | 1992-07-03 | 1994-01-05 | Bayer Ag | Thermoplastische Formmassen |
| DE4328656A1 (de) | 1993-08-26 | 1995-03-02 | Bayer Ag | Flammwidrige, spannungsrißbeständige Polycarbonat-ABS-Formmassen |
| JP3390101B2 (ja) * | 1995-02-23 | 2003-03-24 | 電気化学工業株式会社 | 滞留熱安定性に優れる熱可塑性樹脂組成物およびその製造方法 |
| DE19713039A1 (de) | 1997-03-27 | 1998-10-01 | Bayer Ag | Verfahren zur Herstellung von elastomermodifizierten Thermoplasten |
| US6545089B1 (en) * | 1997-09-04 | 2003-04-08 | General Electric Company | Impact modified carbonnate polymer composition having improved resistance to degradation and improved thermal stability |
| DE19828536A1 (de) | 1998-06-26 | 1999-12-30 | Bayer Ag | Flammwidrige Polycarbonat/ABS-Formmassen |
| DE19941821A1 (de) | 1999-09-02 | 2001-03-08 | Bayer Ag | Flammwidrige Polycarbonat-ABS-Blends |
| JP2002020611A (ja) * | 2000-05-01 | 2002-01-23 | Toray Ind Inc | 難燃性樹脂組成物およびそれからなる成形品 |
| WO2003027165A1 (de) * | 2001-09-21 | 2003-04-03 | Bayer Aktiengesellschaft | Schlagzähmodifizierte polycarbonat-zusammensetzung |
| JPWO2004081114A1 (ja) * | 2003-03-10 | 2006-06-15 | 三菱レイヨン株式会社 | 熱可塑性樹脂組成物 |
| JP2006169461A (ja) * | 2004-12-20 | 2006-06-29 | Toray Ind Inc | ポリカーボネートを含有する熱可塑性樹脂組成物 |
| DE102005058847A1 (de) * | 2005-12-09 | 2007-06-14 | Bayer Materialscience Ag | Polycarbonat-Formmassen |
-
2008
- 2008-12-04 DE DE102008060536A patent/DE102008060536A1/de not_active Withdrawn
-
2009
- 2009-11-21 WO PCT/EP2009/008299 patent/WO2010063381A1/de not_active Ceased
- 2009-11-21 KR KR1020117012756A patent/KR101678240B1/ko not_active Expired - Fee Related
- 2009-11-21 EP EP09763851.4A patent/EP2373743B1/de active Active
- 2009-11-21 JP JP2011538865A patent/JP5705741B2/ja not_active Expired - Fee Related
- 2009-11-21 CA CA2745362A patent/CA2745362C/en not_active Expired - Fee Related
- 2009-11-21 ES ES09763851T patent/ES2428332T3/es active Active
- 2009-11-21 CN CN2009801482808A patent/CN102239218B/zh active Active
- 2009-11-21 MX MX2011005747A patent/MX2011005747A/es active IP Right Grant
- 2009-11-21 BR BRPI0922282A patent/BRPI0922282A2/pt active Search and Examination
- 2009-12-02 US US12/629,342 patent/US7943686B2/en active Active
- 2009-12-03 TW TW098141271A patent/TWI504672B/zh not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| TW201040228A (en) | 2010-11-16 |
| US7943686B2 (en) | 2011-05-17 |
| EP2373743B1 (de) | 2013-07-17 |
| WO2010063381A1 (de) | 2010-06-10 |
| MX2011005747A (es) | 2011-06-20 |
| JP2012511060A (ja) | 2012-05-17 |
| US20100144938A1 (en) | 2010-06-10 |
| CA2745362C (en) | 2017-09-26 |
| EP2373743A1 (de) | 2011-10-12 |
| TWI504672B (zh) | 2015-10-21 |
| CN102239218A (zh) | 2011-11-09 |
| DE102008060536A1 (de) | 2010-06-10 |
| BRPI0922282A2 (pt) | 2015-12-29 |
| CN102239218B (zh) | 2013-05-29 |
| CA2745362A1 (en) | 2010-06-10 |
| JP5705741B2 (ja) | 2015-04-22 |
| KR101678240B1 (ko) | 2016-11-21 |
| KR20110094028A (ko) | 2011-08-19 |
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