JP2006507402A - 衝撃抵抗が改善されたポリマー組成物 - Google Patents
衝撃抵抗が改善されたポリマー組成物 Download PDFInfo
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- JP2006507402A JP2006507402A JP2005510228A JP2005510228A JP2006507402A JP 2006507402 A JP2006507402 A JP 2006507402A JP 2005510228 A JP2005510228 A JP 2005510228A JP 2005510228 A JP2005510228 A JP 2005510228A JP 2006507402 A JP2006507402 A JP 2006507402A
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- 229920006125 amorphous polymer Polymers 0.000 description 1
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- ZPOLOEWJWXZUSP-AATRIKPKSA-N bis(prop-2-enyl) (e)-but-2-enedioate Chemical compound C=CCOC(=O)\C=C\C(=O)OCC=C ZPOLOEWJWXZUSP-AATRIKPKSA-N 0.000 description 1
- ZPOLOEWJWXZUSP-WAYWQWQTSA-N bis(prop-2-enyl) (z)-but-2-enedioate Chemical compound C=CCOC(=O)\C=C/C(=O)OCC=C ZPOLOEWJWXZUSP-WAYWQWQTSA-N 0.000 description 1
- QXJJQWWVWRCVQT-UHFFFAOYSA-K calcium;sodium;phosphate Chemical compound [Na+].[Ca+2].[O-]P([O-])([O-])=O QXJJQWWVWRCVQT-UHFFFAOYSA-K 0.000 description 1
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- QYQADNCHXSEGJT-UHFFFAOYSA-N cyclohexane-1,1-dicarboxylate;hydron Chemical compound OC(=O)C1(C(O)=O)CCCCC1 QYQADNCHXSEGJT-UHFFFAOYSA-N 0.000 description 1
- YQLZOAVZWJBZSY-UHFFFAOYSA-N decane-1,10-diamine Chemical compound NCCCCCCCCCCN YQLZOAVZWJBZSY-UHFFFAOYSA-N 0.000 description 1
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- GDVKFRBCXAPAQJ-UHFFFAOYSA-A dialuminum;hexamagnesium;carbonate;hexadecahydroxide Chemical compound [OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Al+3].[Al+3].[O-]C([O-])=O GDVKFRBCXAPAQJ-UHFFFAOYSA-A 0.000 description 1
- AUTNMGCKBXKHNV-UHFFFAOYSA-P diazanium;3,7-dioxido-2,4,6,8,9-pentaoxa-1,3,5,7-tetraborabicyclo[3.3.1]nonane Chemical compound [NH4+].[NH4+].O1B([O-])OB2OB([O-])OB1O2 AUTNMGCKBXKHNV-UHFFFAOYSA-P 0.000 description 1
- KEIQPMUPONZJJH-UHFFFAOYSA-N dicyclohexylmethanediamine Chemical compound C1CCCCC1C(N)(N)C1CCCCC1 KEIQPMUPONZJJH-UHFFFAOYSA-N 0.000 description 1
- 150000001993 dienes Chemical class 0.000 description 1
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- ZZTCPWRAHWXWCH-UHFFFAOYSA-N diphenylmethanediamine Chemical compound C=1C=CC=CC=1C(N)(N)C1=CC=CC=C1 ZZTCPWRAHWXWCH-UHFFFAOYSA-N 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
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- 239000000839 emulsion Substances 0.000 description 1
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- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
- SUPCQIBBMFXVTL-UHFFFAOYSA-N ethyl 2-methylprop-2-enoate Chemical compound CCOC(=O)C(C)=C SUPCQIBBMFXVTL-UHFFFAOYSA-N 0.000 description 1
- 125000004494 ethyl ester group Chemical group 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
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- 150000002366 halogen compounds Chemical class 0.000 description 1
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- 238000010438 heat treatment Methods 0.000 description 1
- KWLMIXQRALPRBC-UHFFFAOYSA-L hectorite Chemical compound [Li+].[OH-].[OH-].[Na+].[Mg+2].O1[Si]2([O-])O[Si]1([O-])O[Si]([O-])(O1)O[Si]1([O-])O2 KWLMIXQRALPRBC-UHFFFAOYSA-L 0.000 description 1
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- 229910001701 hydrotalcite Inorganic materials 0.000 description 1
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- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
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- 150000002484 inorganic compounds Chemical class 0.000 description 1
- 239000011256 inorganic filler Substances 0.000 description 1
- 229910003475 inorganic filler Inorganic materials 0.000 description 1
- 229910001853 inorganic hydroxide Inorganic materials 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Chemical compound OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
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- 238000000691 measurement method Methods 0.000 description 1
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 1
- RTWNYYOXLSILQN-UHFFFAOYSA-N methanediamine Chemical compound NCN RTWNYYOXLSILQN-UHFFFAOYSA-N 0.000 description 1
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 1
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- 229910017464 nitrogen compound Inorganic materials 0.000 description 1
- 150000002830 nitrogen compounds Chemical class 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
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- 150000002896 organic halogen compounds Chemical class 0.000 description 1
- 235000006408 oxalic acid Nutrition 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- VTRUBDSFZJNXHI-UHFFFAOYSA-N oxoantimony Chemical compound [Sb]=O VTRUBDSFZJNXHI-UHFFFAOYSA-N 0.000 description 1
- PQQKPALAQIIWST-UHFFFAOYSA-N oxomolybdenum Chemical compound [Mo]=O PQQKPALAQIIWST-UHFFFAOYSA-N 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- RVTZCBVAJQQJTK-UHFFFAOYSA-N oxygen(2-);zirconium(4+) Chemical compound [O-2].[O-2].[Zr+4] RVTZCBVAJQQJTK-UHFFFAOYSA-N 0.000 description 1
- 238000007591 painting process Methods 0.000 description 1
- 238000005192 partition Methods 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 150000003018 phosphorus compounds Chemical class 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
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- 239000005020 polyethylene terephthalate Substances 0.000 description 1
- 239000002952 polymeric resin 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
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- 229920003225 polyurethane elastomer Polymers 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000011164 primary particle Substances 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
- 239000010453 quartz Substances 0.000 description 1
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- DCKVNWZUADLDEH-UHFFFAOYSA-N sec-butyl acetate Chemical compound CCC(C)OC(C)=O DCKVNWZUADLDEH-UHFFFAOYSA-N 0.000 description 1
- 238000004062 sedimentation Methods 0.000 description 1
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- 238000007573 shrinkage measurement Methods 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- BPILDHPJSYVNAF-UHFFFAOYSA-M sodium;diiodomethanesulfonate Chemical compound [Na+].[O-]S(=O)(=O)C(I)I BPILDHPJSYVNAF-UHFFFAOYSA-M 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 150000003440 styrenes Chemical class 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 238000010558 suspension polymerization method Methods 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 150000003505 terpenes Chemical class 0.000 description 1
- 235000007586 terpenes Nutrition 0.000 description 1
- 238000009757 thermoplastic moulding Methods 0.000 description 1
- XOLBLPGZBRYERU-UHFFFAOYSA-N tin dioxide Chemical compound O=[Sn]=O XOLBLPGZBRYERU-UHFFFAOYSA-N 0.000 description 1
- 229910001887 tin oxide Inorganic materials 0.000 description 1
- 230000009466 transformation Effects 0.000 description 1
- QDWJJTJNXAKQKD-UHFFFAOYSA-N trihexyphenidyl hydrochloride Chemical compound Cl.C1CCCCC1C(C=1C=CC=CC=1)(O)CCN1CCCCC1 QDWJJTJNXAKQKD-UHFFFAOYSA-N 0.000 description 1
- ZRQNRTRXAVFCMB-UHFFFAOYSA-N tris(2,4,5-trioxa-1-stanna-3-borabicyclo[1.1.1]pentan-1-yl) borate Chemical compound [Sn+4].[Sn+4].[Sn+4].[O-]B([O-])[O-].[O-]B([O-])[O-].[O-]B([O-])[O-].[O-]B([O-])[O-] ZRQNRTRXAVFCMB-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
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
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- 235000005765 wild carrot Nutrition 0.000 description 1
- 229910001928 zirconium oxide Inorganic materials 0.000 description 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L77/00—Compositions of polyamides obtained by reactions forming a carboxylic amide link in the main chain; 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
- 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
- C08L51/06—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 homopolymers or copolymers of aliphatic hydrocarbons containing only one carbon-to-carbon double bond
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L77/00—Compositions of polyamides obtained by reactions forming a carboxylic amide link in the main chain; Compositions of derivatives of such polymers
- C08L77/02—Polyamides derived from omega-amino carboxylic acids or from lactams thereof
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L77/00—Compositions of polyamides obtained by reactions forming a carboxylic amide link in the main chain; Compositions of derivatives of such polymers
- C08L77/06—Polyamides derived from polyamines and polycarboxylic acids
-
- 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
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/02—Elements
- C08K3/04—Carbon
-
- 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
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/34—Silicon-containing compounds
-
- 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
- C08K7/00—Use of ingredients characterised by shape
- C08K7/02—Fibres or whiskers
- C08K7/04—Fibres or whiskers inorganic
- C08K7/10—Silicon-containing compounds
-
- 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
- C08L2205/02—Polymer mixtures characterised by other features containing two or more polymers of the same C08L -group
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L67/00—Compositions of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Compositions of derivatives of such polymers
- C08L67/02—Polyesters derived from dicarboxylic acids and dihydroxy compounds
- C08L67/025—Polyesters derived from dicarboxylic acids and dihydroxy compounds containing polyether sequences
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 |
|---|---|---|---|
| DE2002154877 DE10254877A1 (de) | 2002-11-25 | 2002-11-25 | Schlagzähmodifizierte Polymer-Zusammensetzungen |
| DE2002157077 DE10257077A1 (de) | 2002-12-06 | 2002-12-06 | Schlagzähmodifizierte Polymer-Zusammensetzungen |
| PCT/EP2003/012692 WO2004048474A1 (de) | 2002-11-25 | 2003-11-13 | Schlagzähmodifizierte polymer-zusammensetzungen |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2006507402A true JP2006507402A (ja) | 2006-03-02 |
| JP2006507402A5 JP2006507402A5 (enExample) | 2006-10-26 |
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| JP2005510228A Pending JP2006507402A (ja) | 2002-11-25 | 2003-11-13 | 衝撃抵抗が改善されたポリマー組成物 |
| JP2005510227A Withdrawn JP2006507401A (ja) | 2002-11-25 | 2003-11-13 | 衝撃抵抗が改善されたポリマー組成物 |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
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| JP2005510227A Withdrawn JP2006507401A (ja) | 2002-11-25 | 2003-11-13 | 衝撃抵抗が改善されたポリマー組成物 |
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| US (2) | US20040167264A1 (enExample) |
| EP (2) | EP1567581A1 (enExample) |
| JP (2) | JP2006507402A (enExample) |
| AT (1) | ATE517151T1 (enExample) |
| AU (2) | AU2003279383A1 (enExample) |
| TW (1) | TW200418927A (enExample) |
| WO (2) | WO2004048452A1 (enExample) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
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| WO2013046551A1 (ja) * | 2011-09-28 | 2013-04-04 | 住友ベークライト株式会社 | 成形材料 |
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| Publication number | Priority date | Publication date | Assignee | Title |
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| ATE517151T1 (de) * | 2002-11-25 | 2011-08-15 | Ineos Abs Jersey Ltd | Schlagzähmodifizierte polymer-zusammensetzungen |
| DE10259498A1 (de) * | 2002-12-19 | 2004-07-01 | Bayer Ag | Leitfähige Thermoplaste mit Ruß und Kohlenstoff-Nanofibrillen |
| US7666477B2 (en) * | 2004-03-30 | 2010-02-23 | E.I. Du Pont De Nemours And Company | Process for coating vehicle exterior parts comprising polyamide resins and parts and articles coated thereby |
| JP2008503612A (ja) * | 2004-06-18 | 2008-02-07 | イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニー | カーボンブラックを含有する導電性ポリエーテルエステル組成物およびそれから製造される製品 |
| KR100539065B1 (ko) * | 2004-12-02 | 2005-12-26 | 제일모직주식회사 | 저선팽창성 아크릴로니트릴-부타디엔-스티렌(ａｂｓ) 수지조성물 |
| EP2121843B1 (de) | 2006-12-19 | 2010-08-25 | Basf Se | Thermoplastische formmassen mit verbesserter duktilität |
| US20080153959A1 (en) * | 2006-12-20 | 2008-06-26 | General Electric Company | Thermally Conducting and Electrically Insulating Moldable Compositions and Methods of Manufacture Thereof |
| KR100810966B1 (ko) | 2006-12-29 | 2008-03-10 | 제일모직주식회사 | 폴리아미드계 수지 복합재 |
| US20090187246A1 (en) * | 2008-01-22 | 2009-07-23 | Foley Kevin T | Interbody implants for spinal alignment procedures |
| US20100310851A1 (en) * | 2009-05-18 | 2010-12-09 | Xiaoyun Lai | Conductive Fiber Glass Strands, Methods Of Making The Same, And Composites Comprising The Same |
| US20110178205A1 (en) * | 2010-01-18 | 2011-07-21 | Martin Weber | Process for producing thermoplastic molding compositions based on styrene copolymers and polyamide with improved toughness |
| US20110237693A1 (en) * | 2010-03-23 | 2011-09-29 | Basf Se | Blends made of polyarylene ethers and of polyarylene sulfides |
| JP2013532747A (ja) * | 2010-07-26 | 2013-08-19 | ディーエスエム アイピー アセッツ ビー．ブイ． | 燃料部品および燃料部品の製造方法 |
| DE102010043472A1 (de) * | 2010-11-05 | 2012-05-10 | Evonik Goldschmidt Gmbh | Zusammensetzung aus Polymeren und elektrisch leitfähigem Kohlenstoff |
| US9721695B2 (en) * | 2010-12-21 | 2017-08-01 | Basf Se | Thermoplastic molding composition |
| US20120153232A1 (en) * | 2010-12-21 | 2012-06-21 | Basf Se | Thermoplastic molding composition |
| US8552101B2 (en) | 2011-02-25 | 2013-10-08 | Sabic Innovative Plastics Ip B.V. | Thermally conductive and electrically insulative polymer compositions containing a low thermally conductive filler and uses thereof |
| US8741998B2 (en) * | 2011-02-25 | 2014-06-03 | Sabic Innovative Plastics Ip B.V. | Thermally conductive and electrically insulative polymer compositions containing a thermally insulative filler and uses thereof |
| JP5810619B2 (ja) * | 2011-05-11 | 2015-11-11 | 株式会社カネカ | 熱可塑性樹脂組成物、及びその成形体 |
| EP2920809B1 (en) * | 2012-11-14 | 2021-09-01 | Sun Chemical Corporation | Compositions and processes for fabrication of rear passivated solar cells |
| US20140275366A1 (en) * | 2013-03-13 | 2014-09-18 | Bayer Materialscience Llc | Filled polycarbonate compositions |
| JP6789220B2 (ja) * | 2014-12-24 | 2020-11-25 | モーメンティブ・パフォーマンス・マテリアルズ・インク | 熱伝導性プラスチック組成物、熱伝導性プラスチックを製造するための押出装置および方法 |
| WO2016128067A1 (en) * | 2015-02-13 | 2016-08-18 | Ems-Patent Ag | Polyamide moulding composition and moulded article made from this moulding composition |
| US20180086269A1 (en) * | 2016-09-29 | 2018-03-29 | Magna Mirrors Of America, Inc. | Interior mirror stay formed by gas assist molding process |
| CN108239367A (zh) * | 2016-12-27 | 2018-07-03 | 上海邦中高分子材料有限公司 | 一种用于3d打印的abs材料 |
| KR102125262B1 (ko) * | 2019-01-11 | 2020-06-22 | 주식회사 엘지화학 | 내열성과 전자파 차폐능이 우수한 열가소성 수지 조성물, 이의 제조방법 및 이로부터 제조된 사출성형품 |
| KR102514693B1 (ko) * | 2020-02-28 | 2023-03-27 | 롯데케미칼 주식회사 | 열가소성 수지 조성물 및 이로부터 제조된 성형품 |
| TWI736210B (zh) * | 2020-04-08 | 2021-08-11 | 遠東新世紀股份有限公司 | 聚酯組成物及聚酯片材 |
Family Cites Families (21)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3899462A (en) * | 1974-03-29 | 1975-08-12 | Gen Motors Corp | Reinforced polyamide molding composition |
| US4713415A (en) * | 1985-05-10 | 1987-12-15 | Monsanto Company | Rubber modified nylon composition |
| US5227428A (en) * | 1985-05-10 | 1993-07-13 | Monsanto Company | Rubber modified nylon composition |
| US4974307A (en) * | 1988-06-20 | 1990-12-04 | Mazda Motor Corporation | Method of making an automobile body |
| DE3827669A1 (de) † | 1988-08-16 | 1990-02-22 | Bayer Ag | Thermoplastische interpolymere und ihre verwendung in mischungen aus polyamid und styrol-co- und/oder -pfropfpolymerisaten |
| US5652326A (en) * | 1993-03-03 | 1997-07-29 | Sanyo Chemical Industries, Ltd. | Polyetheresteramide and antistatic resin composition |
| JPH0776634A (ja) * | 1993-09-08 | 1995-03-20 | Yokohama Rubber Co Ltd:The | タイヤトレッド用ゴム組成物 |
| ES2098818T3 (es) * | 1994-06-01 | 1997-05-01 | Gen Electric | Composicion termoplastica que comprende una resina de base de poli(fenileno-eter)-poliamida compatibilizada y negro de carbon electroconductor. |
| DE69513668T2 (de) * | 1994-08-22 | 2000-11-23 | The Dow Chemical Co., Midland | Gefüllte karbonatpolymermischungszusammensetzungen |
| US5484838A (en) * | 1994-12-22 | 1996-01-16 | Ford Motor Company | Thermoplastic compositions with modified electrical conductivity |
| BE1009903A3 (nl) † | 1995-12-29 | 1997-10-07 | Dsm Nv | Rubber gemodificeerde polymeersamenstelling. |
| US5965206A (en) * | 1996-09-16 | 1999-10-12 | Ciba Specialty Chemicals Corporation | Antistatic composition |
| AU9340898A (en) * | 1998-03-05 | 1999-09-20 | Basf Aktiengesellschaft | Polyamide/polyphenylene ether moulding materials with mineral filling materials |
| US6140405A (en) * | 1998-09-21 | 2000-10-31 | The B. F. Goodrich Company | Salt-modified electrostatic dissipative polymers |
| AT407989B (de) * | 1999-10-15 | 2001-07-25 | Solutia Austria Gmbh | Emulgatoren für alkydharzemulsionen mit hohem feststoffgehalt |
| US6469093B1 (en) * | 1999-11-12 | 2002-10-22 | General Electric Company | Conductive polyphenylene ether-polyamide blend |
| AR033370A1 (es) * | 2000-05-19 | 2003-12-17 | Bayer Ag | Una composicion de polimeros modificada con resistencia al impacto, uso de la composicion de polimeros para la produccion de cuerpos moldeados y cuerpos moldeados, piezas de gabinetes, placas de cubiertas y piezas para el sector automotriz obtenibles a partir de la composicion de polimeros. |
| KR100384014B1 (ko) † | 2000-11-30 | 2003-05-14 | 현대자동차주식회사 | 내 가솔린성과 내한 충격성이 우수한 폴리아미드 수지조성물 |
| FR2824329B1 (fr) * | 2001-05-03 | 2003-06-13 | Atofina | Compositions de polymeres antistatique |
| DE10233170A1 (de) * | 2002-07-22 | 2004-02-12 | Bayer Ag | Polymerblends auf Basis Polyamid |
| ATE517151T1 (de) * | 2002-11-25 | 2011-08-15 | Ineos Abs Jersey Ltd | Schlagzähmodifizierte polymer-zusammensetzungen |
-
2003
- 2003-11-13 AT AT03772334T patent/ATE517151T1/de active
- 2003-11-13 JP JP2005510228A patent/JP2006507402A/ja active Pending
- 2003-11-13 EP EP03772333A patent/EP1567581A1/de not_active Withdrawn
- 2003-11-13 AU AU2003279383A patent/AU2003279383A1/en not_active Abandoned
- 2003-11-13 WO PCT/EP2003/012691 patent/WO2004048452A1/de not_active Ceased
- 2003-11-13 AU AU2003279385A patent/AU2003279385A1/en not_active Abandoned
- 2003-11-13 WO PCT/EP2003/012692 patent/WO2004048474A1/de not_active Ceased
- 2003-11-13 EP EP03772334.3A patent/EP1567591B2/de not_active Expired - Lifetime
- 2003-11-13 JP JP2005510227A patent/JP2006507401A/ja not_active Withdrawn
- 2003-11-21 US US10/719,403 patent/US20040167264A1/en not_active Abandoned
- 2003-11-21 US US10/719,720 patent/US20040167268A1/en not_active Abandoned
- 2003-11-24 TW TW092132852A patent/TW200418927A/zh unknown
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2013046551A1 (ja) * | 2011-09-28 | 2013-04-04 | 住友ベークライト株式会社 | 成形材料 |
| JPWO2013046551A1 (ja) * | 2011-09-28 | 2015-03-26 | 住友ベークライト株式会社 | 成形材料 |
Also Published As
| Publication number | Publication date |
|---|---|
| EP1567591B1 (de) | 2011-07-20 |
| US20040167268A1 (en) | 2004-08-26 |
| WO2004048474A1 (de) | 2004-06-10 |
| EP1567581A1 (de) | 2005-08-31 |
| AU2003279385A1 (en) | 2004-06-18 |
| EP1567591B2 (de) | 2015-10-21 |
| TW200418927A (en) | 2004-10-01 |
| ATE517151T1 (de) | 2011-08-15 |
| EP1567591A1 (de) | 2005-08-31 |
| JP2006507401A (ja) | 2006-03-02 |
| US20040167264A1 (en) | 2004-08-26 |
| WO2004048452A1 (de) | 2004-06-10 |
| AU2003279383A1 (en) | 2004-06-18 |
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