MXPA01009576A - Composiciones que contienen policarbonato y caucho injertado y que presentan una tenacidad mejorada. - Google Patents
Composiciones que contienen policarbonato y caucho injertado y que presentan una tenacidad mejorada.Info
- Publication number
- MXPA01009576A MXPA01009576A MXPA01009576A MXPA01009576A MXPA01009576A MX PA01009576 A MXPA01009576 A MX PA01009576A MX PA01009576 A MXPA01009576 A MX PA01009576A MX PA01009576 A MXPA01009576 A MX PA01009576A MX PA01009576 A MXPA01009576 A MX PA01009576A
- Authority
- MX
- Mexico
- Prior art keywords
- weight
- molding composition
- composition according
- thermoplastic molding
- component
- Prior art date
Links
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- BCKXLBQYZLBQEK-KVVVOXFISA-M Sodium oleate Chemical compound [Na+].CCCCCCCC\C=C/CCCCCCCC([O-])=O BCKXLBQYZLBQEK-KVVVOXFISA-M 0.000 description 1
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- 125000002993 cycloalkylene group Chemical group 0.000 description 1
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- 125000004386 diacrylate group Chemical group 0.000 description 1
- JBSLOWBPDRZSMB-FPLPWBNLSA-N dibutyl (z)-but-2-enedioate Chemical compound CCCCOC(=O)\C=C/C(=O)OCCCC JBSLOWBPDRZSMB-FPLPWBNLSA-N 0.000 description 1
- 229920003244 diene elastomer Polymers 0.000 description 1
- 150000001993 dienes Chemical class 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- LDCRTTXIJACKKU-ARJAWSKDSA-N dimethyl maleate Chemical compound COC(=O)\C=C/C(=O)OC LDCRTTXIJACKKU-ARJAWSKDSA-N 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- QZYRMODBFHTNHF-UHFFFAOYSA-N ditert-butyl benzene-1,2-dicarboperoxoate Chemical compound CC(C)(C)OOC(=O)C1=CC=CC=C1C(=O)OOC(C)(C)C QZYRMODBFHTNHF-UHFFFAOYSA-N 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- AFSIMBWBBOJPJG-UHFFFAOYSA-N ethenyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OC=C AFSIMBWBBOJPJG-UHFFFAOYSA-N 0.000 description 1
- UIWXSTHGICQLQT-UHFFFAOYSA-N ethenyl propanoate Chemical compound CCC(=O)OC=C UIWXSTHGICQLQT-UHFFFAOYSA-N 0.000 description 1
- 125000002573 ethenylidene group Chemical group [*]=C=C([H])[H] 0.000 description 1
- STVZJERGLQHEKB-UHFFFAOYSA-N ethylene glycol dimethacrylate Substances CC(=C)C(=O)OCCOC(=O)C(C)=C STVZJERGLQHEKB-UHFFFAOYSA-N 0.000 description 1
- 238000011156 evaluation Methods 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
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 229910052736 halogen Chemical group 0.000 description 1
- 150000002367 halogens Chemical group 0.000 description 1
- PBZROIMXDZTJDF-UHFFFAOYSA-N hepta-1,6-dien-4-one Chemical compound C=CCC(=O)CC=C PBZROIMXDZTJDF-UHFFFAOYSA-N 0.000 description 1
- DMEGYFMYUHOHGS-UHFFFAOYSA-N heptamethylene Natural products C1CCCCCC1 DMEGYFMYUHOHGS-UHFFFAOYSA-N 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 239000012943 hotmelt Substances 0.000 description 1
- GRKJHYSEVIVDBO-UHFFFAOYSA-N hydrogen peroxide;pentane Chemical compound OO.CCCCC GRKJHYSEVIVDBO-UHFFFAOYSA-N 0.000 description 1
- 125000004464 hydroxyphenyl group Chemical group 0.000 description 1
- 238000009863 impact test Methods 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 150000002688 maleic acid derivatives Chemical class 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- GYNNXHKOJHMOHS-UHFFFAOYSA-N methyl-cycloheptane Natural products CC1CCCCCC1 GYNNXHKOJHMOHS-UHFFFAOYSA-N 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 239000003607 modifier Substances 0.000 description 1
- 239000006082 mold release agent Substances 0.000 description 1
- YRVUCYWJQFRCOB-UHFFFAOYSA-N n-butylprop-2-enamide Chemical compound CCCCNC(=O)C=C YRVUCYWJQFRCOB-UHFFFAOYSA-N 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 125000004430 oxygen atom Chemical group O* 0.000 description 1
- SJDACOMXKWHBOW-UHFFFAOYSA-N oxyphenisatine Chemical compound C1=CC(O)=CC=C1C1(C=2C=CC(O)=CC=2)C2=CC=CC=C2NC1=O SJDACOMXKWHBOW-UHFFFAOYSA-N 0.000 description 1
- HFPZCAJZSCWRBC-UHFFFAOYSA-N p-cymene Chemical compound CC(C)C1=CC=C(C)C=C1 HFPZCAJZSCWRBC-UHFFFAOYSA-N 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- JRKICGRDRMAZLK-UHFFFAOYSA-L persulfate group Chemical group S(=O)(=O)([O-])OOS(=O)(=O)[O-] JRKICGRDRMAZLK-UHFFFAOYSA-L 0.000 description 1
- QCDYQQDYXPDABM-UHFFFAOYSA-N phloroglucinol Chemical compound OC1=CC(O)=CC(O)=C1 QCDYQQDYXPDABM-UHFFFAOYSA-N 0.000 description 1
- 229960001553 phloroglucinol Drugs 0.000 description 1
- PMJHHCWVYXUKFD-UHFFFAOYSA-N piperylene Natural products CC=CC=C PMJHHCWVYXUKFD-UHFFFAOYSA-N 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920002587 poly(1,3-butadiene) polymer Polymers 0.000 description 1
- 229920002857 polybutadiene Polymers 0.000 description 1
- FBCQUCJYYPMKRO-UHFFFAOYSA-N prop-2-enyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCC=C FBCQUCJYYPMKRO-UHFFFAOYSA-N 0.000 description 1
- QTECDUFMBMSHKR-UHFFFAOYSA-N prop-2-enyl prop-2-enoate Chemical compound C=CCOC(=O)C=C QTECDUFMBMSHKR-UHFFFAOYSA-N 0.000 description 1
- HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical compound C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 description 1
- AHIHJODVQGBOND-UHFFFAOYSA-M propan-2-yl carbonate Chemical compound CC(C)OC([O-])=O AHIHJODVQGBOND-UHFFFAOYSA-M 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- 150000003222 pyridines Chemical class 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 239000007870 radical polymerization initiator Substances 0.000 description 1
- 238000010526 radical polymerization reaction Methods 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- RYYKJJJTJZKILX-UHFFFAOYSA-M sodium octadecanoate Chemical compound [Na+].CCCCCCCCCCCCCCCCCC([O-])=O RYYKJJJTJZKILX-UHFFFAOYSA-M 0.000 description 1
- 229940045870 sodium palmitate Drugs 0.000 description 1
- 229940080350 sodium stearate Drugs 0.000 description 1
- GGXKEBACDBNFAF-UHFFFAOYSA-M sodium;hexadecanoate Chemical compound [Na+].CCCCCCCCCCCCCCCC([O-])=O GGXKEBACDBNFAF-UHFFFAOYSA-M 0.000 description 1
- MWNQXXOSWHCCOZ-UHFFFAOYSA-L sodium;oxido carbonate Chemical class [Na+].[O-]OC([O-])=O MWNQXXOSWHCCOZ-UHFFFAOYSA-L 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 150000003440 styrenes Chemical class 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 150000003871 sulfonates Chemical class 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 125000004434 sulfur atom Chemical group 0.000 description 1
- 238000010557 suspension polymerization reaction Methods 0.000 description 1
- 238000001308 synthesis method Methods 0.000 description 1
- 150000003505 terpenes Chemical class 0.000 description 1
- 235000007586 terpenes Nutrition 0.000 description 1
- NMOALOSNPWTWRH-UHFFFAOYSA-N tert-butyl 7,7-dimethyloctaneperoxoate Chemical compound CC(C)(C)CCCCCC(=O)OOC(C)(C)C NMOALOSNPWTWRH-UHFFFAOYSA-N 0.000 description 1
- GJBRNHKUVLOCEB-UHFFFAOYSA-N tert-butyl benzenecarboperoxoate Chemical compound CC(C)(C)OOC(=O)C1=CC=CC=C1 GJBRNHKUVLOCEB-UHFFFAOYSA-N 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- 238000005809 transesterification reaction Methods 0.000 description 1
- FUSUHKVFWTUUBE-UHFFFAOYSA-N vinyl methyl ketone Natural products CC(=O)C=C FUSUHKVFWTUUBE-UHFFFAOYSA-N 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 239000004711 α-olefin Substances 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
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L25/00—Compositions of, homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an aromatic carbocyclic ring; Compositions of derivatives of such polymers
- C08L25/02—Homopolymers or copolymers of hydrocarbons
- C08L25/04—Homopolymers or copolymers of styrene
- C08L25/08—Copolymers of styrene
- C08L25/12—Copolymers of styrene with unsaturated nitriles
-
- 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
- C08L55/00—Compositions of homopolymers or copolymers, obtained by polymerisation reactions only involving carbon-to-carbon unsaturated bonds, not provided for in groups C08L23/00 - C08L53/00
- C08L55/02—ABS [Acrylonitrile-Butadiene-Styrene] polymers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2300/00—Characterised by the use of unspecified polymers
- C08J2300/22—Thermoplastic resins
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2205/00—Polymer mixtures characterised by other features
- C08L2205/03—Polymer mixtures characterised by other features containing three or more polymers in a blend
- C08L2205/035—Polymer mixtures characterised by other features containing three or more polymers in a blend containing four or more polymers in a blend
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2666/00—Composition of polymers characterized by a further compound in the blend, being organic macromolecular compounds, natural resins, waxes or and bituminous materials, non-macromolecular organic substances, inorganic substances or characterized by their function in the composition
- C08L2666/02—Organic macromolecular compounds, natural resins, waxes or and bituminous materials
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 (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US27621599A | 1999-03-25 | 1999-03-25 | |
| PCT/US2000/007616 WO2000056816A1 (en) | 1999-03-25 | 2000-03-21 | Compositions containing polycarbonate and grafted rubber having improved low-temperature toughness |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MXPA01009576A true MXPA01009576A (es) | 2002-03-14 |
Family
ID=23055685
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MXPA01009576A MXPA01009576A (es) | 1999-03-25 | 2000-03-21 | Composiciones que contienen policarbonato y caucho injertado y que presentan una tenacidad mejorada. |
Country Status (15)
| Country | Link |
|---|---|
| EP (1) | EP1185585B1 (enExample) |
| JP (1) | JP4587568B2 (enExample) |
| KR (1) | KR20010108382A (enExample) |
| CN (1) | CN1160411C (enExample) |
| AR (1) | AR023137A1 (enExample) |
| AT (1) | ATE334171T1 (enExample) |
| AU (1) | AU4326100A (enExample) |
| BR (1) | BR0009208B1 (enExample) |
| CA (1) | CA2365270A1 (enExample) |
| DE (1) | DE60029587T2 (enExample) |
| ES (1) | ES2267523T3 (enExample) |
| HK (1) | HK1045706A1 (enExample) |
| MX (1) | MXPA01009576A (enExample) |
| TW (1) | TWI230727B (enExample) |
| WO (1) | WO2000056816A1 (enExample) |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE10060410A1 (de) | 2000-12-05 | 2002-06-06 | Bayer Ag | Thermoplastische Formmassen |
| DE10223646A1 (de) * | 2002-05-28 | 2003-12-11 | Bayer Ag | Verfahren zur Herstellung von ABS-Zusammensetzungen mit verbesserten Zähigkeitseigenschaften |
| US6730748B2 (en) * | 2002-07-09 | 2004-05-04 | Bayer Polymers Llc | Thermoplastic polycarbonate compositions having high toughness |
| CN100386378C (zh) * | 2005-06-10 | 2008-05-07 | 上海华谊本体聚合技术开发有限公司 | 一种高抗冲高耐热共混abs树脂的制备方法 |
| JP5758649B2 (ja) * | 2011-02-22 | 2015-08-05 | 三菱エンジニアリングプラスチックス株式会社 | ポリカーボネート樹脂組成物及び成形体 |
| CN102746631B (zh) * | 2011-04-20 | 2015-01-07 | 中国石油化工股份有限公司 | 耐低温冲击的聚碳酸酯/abs树脂塑料合金 |
| EP2647669A1 (de) * | 2012-04-05 | 2013-10-09 | Bayer MaterialScience AG | Schlagzähmodifizierte Polycarbonat-Zusammensetzungen zur vereinfachten Herstellung von tieftemperaturzähen Bauteilen mit hochglänzenden und matten Bauteilabschnitten |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4677162A (en) * | 1983-04-15 | 1987-06-30 | Mobay Corporation | Polycarbonate blends having low gloss |
| DE3339001A1 (de) * | 1983-07-06 | 1985-01-17 | Bayer Ag, 5090 Leverkusen | Thermoplastische polyester-formmassen mit hoher zaehigkeit |
| DE3615607A1 (de) * | 1986-05-09 | 1987-11-12 | Basf Ag | Thermoplastische formmasse auf basis von polycarbonat, asa und vinylaromaten/an enthaltenden copolymerisaten |
| DE3735754A1 (de) * | 1987-10-22 | 1989-05-03 | Basf Ag | Thermoplastische formmasse, verfahren zu ihrer herstellung und deren verwendung |
| DE3939046A1 (de) * | 1989-11-25 | 1991-05-29 | Basf Ag | Thermoplastische formmassen mit hoher kaeltezaehigkeit |
| DE4221935A1 (de) * | 1992-07-03 | 1994-01-05 | Bayer Ag | Thermoplastische Formmassen |
| JP3384902B2 (ja) * | 1995-01-13 | 2003-03-10 | 住友ダウ株式会社 | 難燃性熱可塑性樹脂組成物 |
-
2000
- 2000-03-14 TW TW089104537A patent/TWI230727B/zh not_active IP Right Cessation
- 2000-03-21 EP EP00923080A patent/EP1185585B1/en not_active Expired - Lifetime
- 2000-03-21 JP JP2000606676A patent/JP4587568B2/ja not_active Expired - Fee Related
- 2000-03-21 DE DE60029587T patent/DE60029587T2/de not_active Expired - Lifetime
- 2000-03-21 KR KR1020017012122A patent/KR20010108382A/ko not_active Ceased
- 2000-03-21 AU AU43261/00A patent/AU4326100A/en not_active Abandoned
- 2000-03-21 CN CNB008055068A patent/CN1160411C/zh not_active Expired - Lifetime
- 2000-03-21 HK HK02107330.2A patent/HK1045706A1/zh unknown
- 2000-03-21 CA CA002365270A patent/CA2365270A1/en not_active Abandoned
- 2000-03-21 MX MXPA01009576A patent/MXPA01009576A/es active IP Right Grant
- 2000-03-21 ES ES00923080T patent/ES2267523T3/es not_active Expired - Lifetime
- 2000-03-21 WO PCT/US2000/007616 patent/WO2000056816A1/en not_active Ceased
- 2000-03-21 AT AT00923080T patent/ATE334171T1/de not_active IP Right Cessation
- 2000-03-21 BR BRPI0009208-8A patent/BR0009208B1/pt not_active IP Right Cessation
- 2000-03-22 AR ARP000101291A patent/AR023137A1/es not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| TWI230727B (en) | 2005-04-11 |
| AU4326100A (en) | 2000-10-09 |
| HK1045706A1 (zh) | 2002-12-06 |
| DE60029587D1 (de) | 2006-09-07 |
| AR023137A1 (es) | 2002-09-04 |
| ATE334171T1 (de) | 2006-08-15 |
| ES2267523T3 (es) | 2007-03-16 |
| EP1185585B1 (en) | 2006-07-26 |
| BR0009208A (pt) | 2001-12-26 |
| BR0009208B1 (pt) | 2010-08-24 |
| EP1185585A1 (en) | 2002-03-13 |
| DE60029587T2 (de) | 2007-08-09 |
| JP2002540241A (ja) | 2002-11-26 |
| CA2365270A1 (en) | 2000-09-28 |
| KR20010108382A (ko) | 2001-12-07 |
| WO2000056816A1 (en) | 2000-09-28 |
| CN1160411C (zh) | 2004-08-04 |
| CN1345355A (zh) | 2002-04-17 |
| JP4587568B2 (ja) | 2010-11-24 |
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| Date | Code | Title | Description |
|---|---|---|---|
| FG | Grant or registration |