CN1717453A - 冲击改性共混物 - Google Patents
冲击改性共混物 Download PDFInfo
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- CN1717453A CN1717453A CNA2003801045921A CN200380104592A CN1717453A CN 1717453 A CN1717453 A CN 1717453A CN A2003801045921 A CNA2003801045921 A CN A2003801045921A CN 200380104592 A CN200380104592 A CN 200380104592A CN 1717453 A CN1717453 A CN 1717453A
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Images
Classifications
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- 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
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- 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
- C08F279/00—Macromolecular compounds obtained by polymerising monomers on to polymers of monomers having two or more carbon-to-carbon double bonds as defined in group C08F36/00
- C08F279/02—Macromolecular compounds obtained by polymerising monomers on to polymers of monomers having two or more carbon-to-carbon double bonds as defined in group C08F36/00 on to polymers of conjugated dienes
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- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
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- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Manufacturing & Machinery (AREA)
- Materials Engineering (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Processes Of Treating Macromolecular Substances (AREA)
Abstract
Description
组分(重量份) | 1 | 2 | 3 | 4(对比) | 5(对比) | 6(对比) |
A1 | 43 | 43 | 43 | 43 | 43 | 43 |
B1.1 | - | - | - | 24 | - | - |
B2.1 | - | - | - | - | 24.8 | - |
B2.2 | - | - | - | - | - | 19.2 |
共沉淀产物B1.1/B2.1=75∶25 | 24.2 | - | - | - | - | - |
共沉淀产物B1.1/B2.1=50∶50 | - | 24.4 | - | - | - | - |
共沉淀产物B1.1/B2.2=75∶25 | - | - | 22.6 | - | - | - |
B3 | 32.8 | 32.6 | 34.4 | 33 | 32.2 | 37.8 |
E1 | 0.75 | 0.75 | 0.75 | 0.75 | 0.75 | 0.75 |
E2 | 0.12 | 0.12 | 0.12 | 0.12 | 0.12 | 0.12 |
ak -20℃(kJ/m2) | 68 | 77 | 69 | 73 | 65 | 16 |
MVR(cm3/10min) | 9.9 | 12.6 | 10.8 | 7.8 | 17.6 | 17.2 |
ESC特性在εx(%)下的断裂 | 2.4 | 2.4 | 2.4 | 2.4 | 0.4 | 1.8 |
表面 | ++ | + | + | -- | o | - |
组分(重量份) | 7 | 8 | 9 | 10(对比) | 11(对比) | 12(对比) |
A1 | 58 | 58 | 58 | 58 | 58 | 58 |
B1.1 | - | - | - | 18 | - | - |
B2.1 | - | - | - | - | 18.6 | - |
B2.2 | - | - | - | - | - | 14.4 |
共沉淀产物B1.1/B2.1=75∶25 | 18.2 | - | - | - | - | - |
共沉淀产物B1.1/B2.1=50∶50 | - | 18.3 | - | - | - | - |
共沉淀产物B1.1/B2.2=75∶25 | - | - | 16.9 | - | - | - |
B3 | 23.8 | 23.7 | 25.1 | 24 | 23.4 | 27.6 |
E1 | 0.75 | 0.75 | 0.75 | 0.75 | 0.75 | 0.75 |
E2 | 0.12 | 0.12 | 0.12 | 0.12 | 0.12 | 0.12 |
ak -20℃(kJ/m2) | 93 | 96 | 87 | 87 | 93 | 53 |
MVR(cm3/10min) | 11.9 | 13.4 | 11.8 | 9.8 | 16.6 | 17.1 |
ESC特性在εx(%)下的断裂 | 2.4 | 2.4 | 2.2 | 2.4 | 0.4 | 0.6 |
表面 | ++ | ++ | + | -- | o | - |
组分(重量份) | 13 | 14 | 15(对比) | 16(对比) | 17(对比) |
A1 | 52.3 | 52.3 | 52.3 | 52.3 | 52.3 |
A2 | 16.0 | 16.0 | 16.0 | 16.0 | 16.0 |
B1.1 | - | - | 9.3 | - | - |
B2.1 | - | - | - | 9.6 | - |
B2.2 | - | - | - | - | 7.4 |
共沉淀产物B1.1/B2.1=75∶25 | 9.4 | - | - | - | - |
共沉淀产物B1.1/B2.2=75∶25 | - | 8.8 | - | - | - |
B3 | 7.5 | 8.1 | 7.6 | 7.3 | 9.5 |
C1 | 3.4 | 3.4 | 3.4 | 3.4 | 3.4 |
C2 | 10.1 | 10.1 | 10.1 | 10.1 | 10.1 |
D | 0.8 | 0.8 | 0.8 | 0.8 | 0.8 |
E1 | 0.4 | 0.4 | 0.4 | 0.4 | 0.4 |
E2 | 0.1 | 0.1 | 0.1 | 0.1 | 0.1 |
ak RT(kJ/m2) | 44 | 41 | 47 | 12 | 11 |
MVR(cm3/10min) | 22 | 22 | 21 | 25 | 25 |
ESC特性:εx(%) | 2.0 | 2.0 | 2.0 | 2.0 | 1.8 |
UL 94V,1.5min | V-0 | n.d. | V-0 | V-0 | n.d. |
后烧时间(s) | 4 | n.d. | 5 | 3 | n.d. |
表面 | ++ | ++ | o | o | o |
组分(重量份) | 18 | 19(对比) |
A1 | 54 | 54 |
A2 | 4 | 4 |
B1.1/B2.1-B3 | 36 | - |
B1.1-B3 | - | 36 |
B3 | 6 | 6 |
E1 | 0.75 | 0.75 |
E2 | 0.12 | 0.12 |
表面 | +参看图1 | --参看图2 |
Claims (27)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
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DE10255824A DE10255824A1 (de) | 2002-11-29 | 2002-11-29 | Schlagzähmodifizierte Blends |
DE10255824.8 | 2002-11-29 |
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CN1717453A true CN1717453A (zh) | 2006-01-04 |
CN100471914C CN100471914C (zh) | 2009-03-25 |
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CNB2003801045921A Expired - Lifetime CN100471914C (zh) | 2002-11-29 | 2003-11-17 | 冲击改性共混物 |
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Country | Link |
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US (1) | US7790805B2 (zh) |
EP (1) | EP1567596B1 (zh) |
JP (1) | JP4732758B2 (zh) |
KR (1) | KR100985981B1 (zh) |
CN (1) | CN100471914C (zh) |
AT (1) | ATE384770T1 (zh) |
AU (1) | AU2003296577A1 (zh) |
BR (1) | BR0316689B1 (zh) |
CA (1) | CA2507623C (zh) |
DE (2) | DE10255824A1 (zh) |
ES (1) | ES2299762T3 (zh) |
HK (1) | HK1086849A1 (zh) |
MX (1) | MXPA05005604A (zh) |
WO (1) | WO2004050765A1 (zh) |
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CN101845210B (zh) * | 2009-03-25 | 2012-10-03 | 上海锦湖日丽塑料有限公司 | 一种聚碳酸酯/聚酰胺合金及其制备方法 |
CN102015891B (zh) * | 2008-04-24 | 2015-04-29 | 拜尔材料科学股份公司 | 高耐水解和浅本色的冲击改性聚碳酸酯组合物 |
WO2016037353A1 (en) * | 2014-09-12 | 2016-03-17 | Arkema (Changshu) Fluorochemical Co., Ltd. | Method for preparing a grafted unsaturated synthetic rubber |
CN110088195A (zh) * | 2016-12-28 | 2019-08-02 | 科思创德国股份有限公司 | 具有好的低温韧性、高光泽度和高加工稳定性的组合物和热塑性模塑料 |
CN111601829A (zh) * | 2017-11-13 | 2020-08-28 | 英力士苯领集团股份公司 | 具有改善的表面质量的热塑性模塑组合物及其制品 |
Families Citing this family (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE10255824A1 (de) * | 2002-11-29 | 2004-06-09 | Bayer Ag | Schlagzähmodifizierte Blends |
US20070093395A1 (en) * | 2005-10-21 | 2007-04-26 | Habeeb Jacob J | Antiwear inhibiting and load enhancing additive combinations for lubricating oils |
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US20110274932A1 (en) * | 2010-05-05 | 2011-11-10 | Basf Se | Component comprising an insert part and plastics jacketing, and process for production of the component |
WO2011156663A1 (en) | 2010-06-10 | 2011-12-15 | Abs Materials,Inc | Method of treating a material using a sol-gel derived composition |
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WO2016184765A1 (de) * | 2015-05-18 | 2016-11-24 | Ineos Styrolution Group Gmbh | Abs-formmasse mit guter eigenschaftskombination von verarbeitbarkeit und oberflächenqualität |
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Family Cites Families (17)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3130177A (en) | 1961-03-24 | 1964-04-21 | Borg Warner | Blends of polycarbonates with polybutadiene, styrene, acrylonitrile graft copolymers |
US3988389A (en) | 1972-12-06 | 1976-10-26 | Bayer Aktiengesellschaft | Moulding compositions contain polycarbonate and graft copolymer of a resin forming monomer on a rubber |
US3954905A (en) | 1973-06-09 | 1976-05-04 | Bayer Aktiengesellschaft | Moulding composition of a polycarbonate, a graft copolymer and a copolymer and moulded articles therefrom |
DE2818679A1 (de) | 1978-04-27 | 1979-10-31 | Bayer Ag | Thermoplastische formmassen |
JPS581743A (ja) * | 1981-06-25 | 1983-01-07 | Hitachi Chem Co Ltd | 耐熱性熱可塑性樹脂組成物 |
US4747959A (en) | 1987-04-13 | 1988-05-31 | Polysar Limited | Analytical method and apparatus for characterizing latexes |
DE4126483A1 (de) | 1991-08-10 | 1993-02-11 | Bayer Ag | Verfahren zur aufkonzentrierung von latex-dispersionen |
US5221713A (en) * | 1991-10-07 | 1993-06-22 | Rohm And Haas Company | Co-microagglomeration of emulsion polymers (encapsulated core/shell additives for pvc) |
DE4434965A1 (de) * | 1994-09-30 | 1996-04-04 | Bayer Ag | Polycarbonat-Formmassen mit verbesserter Zähigkeit |
ES2267272T3 (es) * | 1998-07-27 | 2007-03-01 | General Electric Company | Mezcla de resinas de copolimeros de injerto modificados con caucho/policarbonato retardante de llama con aspecto metalico. |
DE19941491A1 (de) * | 1999-09-01 | 2001-03-15 | Bayer Ag | Thermoplastische Formmassen auf Basis bestimmter Pfropfkautschukkomponenten |
JP4702998B2 (ja) * | 2000-12-05 | 2011-06-15 | 株式会社カネカ | ゴム変性樹脂およびそれを含有する熱可塑性樹脂組成物 |
DE10061080A1 (de) * | 2000-12-08 | 2002-06-13 | Bayer Ag | Polycarbonat-Zusammensetzungen |
JP2002308997A (ja) * | 2001-04-12 | 2002-10-23 | Mitsubishi Rayon Co Ltd | ゴム質重合体含有材料 |
JP2002327177A (ja) * | 2001-04-27 | 2002-11-15 | Mitsubishi Rayon Co Ltd | 難燃剤および難燃性樹脂組成物 |
JP4111511B2 (ja) * | 2002-09-30 | 2008-07-02 | テクノポリマー株式会社 | ゴム強化ビニル系樹脂、ゴム強化ビニル系樹脂の製造方法、ゴム強化ビニル系樹脂組成物 |
DE10255824A1 (de) * | 2002-11-29 | 2004-06-09 | Bayer Ag | Schlagzähmodifizierte Blends |
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Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
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CN102015891B (zh) * | 2008-04-24 | 2015-04-29 | 拜尔材料科学股份公司 | 高耐水解和浅本色的冲击改性聚碳酸酯组合物 |
TWI551649B (zh) * | 2008-04-24 | 2016-10-01 | 科思創德意志股份有限公司 | 具高耐水解性和淺的自然顏色之衝擊性改質聚碳酸酯組成物 |
CN101845210B (zh) * | 2009-03-25 | 2012-10-03 | 上海锦湖日丽塑料有限公司 | 一种聚碳酸酯/聚酰胺合金及其制备方法 |
WO2016037353A1 (en) * | 2014-09-12 | 2016-03-17 | Arkema (Changshu) Fluorochemical Co., Ltd. | Method for preparing a grafted unsaturated synthetic rubber |
CN110088195A (zh) * | 2016-12-28 | 2019-08-02 | 科思创德国股份有限公司 | 具有好的低温韧性、高光泽度和高加工稳定性的组合物和热塑性模塑料 |
CN110088195B (zh) * | 2016-12-28 | 2022-09-06 | 科思创德国股份有限公司 | 具有好的低温韧性、高光泽度和高加工稳定性的组合物和热塑性模塑料 |
CN111601829A (zh) * | 2017-11-13 | 2020-08-28 | 英力士苯领集团股份公司 | 具有改善的表面质量的热塑性模塑组合物及其制品 |
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DE50309095D1 (de) | 2008-03-13 |
JP4732758B2 (ja) | 2011-07-27 |
ES2299762T3 (es) | 2008-06-01 |
EP1567596B1 (de) | 2008-01-23 |
ATE384770T1 (de) | 2008-02-15 |
CA2507623C (en) | 2012-01-24 |
HK1086849A1 (en) | 2006-09-29 |
DE10255824A1 (de) | 2004-06-09 |
US20040132905A1 (en) | 2004-07-08 |
KR100985981B1 (ko) | 2010-10-06 |
BR0316689B1 (pt) | 2014-01-28 |
CN100471914C (zh) | 2009-03-25 |
US7790805B2 (en) | 2010-09-07 |
KR20050084013A (ko) | 2005-08-26 |
EP1567596A1 (de) | 2005-08-31 |
BR0316689A (pt) | 2005-10-18 |
CA2507623A1 (en) | 2004-06-17 |
AU2003296577A1 (en) | 2004-06-23 |
JP2006508219A (ja) | 2006-03-09 |
MXPA05005604A (es) | 2005-07-27 |
WO2004050765A1 (de) | 2004-06-17 |
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