CN102822276A - 聚碳酸酯树脂组合物、其制造方法以及该树脂组合物的成型体 - Google Patents
聚碳酸酯树脂组合物、其制造方法以及该树脂组合物的成型体 Download PDFInfo
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- CN102822276A CN102822276A CN2011800166016A CN201180016601A CN102822276A CN 102822276 A CN102822276 A CN 102822276A CN 2011800166016 A CN2011800166016 A CN 2011800166016A CN 201180016601 A CN201180016601 A CN 201180016601A CN 102822276 A CN102822276 A CN 102822276A
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- polycarbonate resin
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- poly carbonate
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- 125000005543 phthalimide group Chemical class 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 230000037048 polymerization activity Effects 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 239000001205 polyphosphate Substances 0.000 description 1
- 235000011176 polyphosphates Nutrition 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 239000001103 potassium chloride Substances 0.000 description 1
- 235000011164 potassium chloride Nutrition 0.000 description 1
- 238000004094 preconcentration Methods 0.000 description 1
- 238000007639 printing Methods 0.000 description 1
- JTTWNTXHFYNETH-UHFFFAOYSA-N propyl 4-methylbenzenesulfonate Chemical compound CCCOS(=O)(=O)C1=CC=C(C)C=C1 JTTWNTXHFYNETH-UHFFFAOYSA-N 0.000 description 1
- OCNPXKLQSGAGKT-UHFFFAOYSA-N propyl benzenesulfonate Chemical compound CCCOS(=O)(=O)C1=CC=CC=C1 OCNPXKLQSGAGKT-UHFFFAOYSA-N 0.000 description 1
- NNOBHPBYUHDMQF-UHFFFAOYSA-N propylphosphine Chemical class CCCP NNOBHPBYUHDMQF-UHFFFAOYSA-N 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 150000003222 pyridines Chemical class 0.000 description 1
- VTGOHKSTWXHQJK-UHFFFAOYSA-N pyrimidin-2-ol Chemical compound OC1=NC=CC=N1 VTGOHKSTWXHQJK-UHFFFAOYSA-N 0.000 description 1
- 230000036632 reaction speed Effects 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 230000002441 reversible effect Effects 0.000 description 1
- 230000002000 scavenging effect Effects 0.000 description 1
- 230000035939 shock Effects 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000002210 silicon-based material Substances 0.000 description 1
- 229920002050 silicone resin Polymers 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 238000000935 solvent evaporation Methods 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 159000000008 strontium salts Chemical class 0.000 description 1
- 150000005846 sugar alcohols Chemical class 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- KUCOHFSKRZZVRO-UHFFFAOYSA-N terephthalaldehyde Chemical compound O=CC1=CC=C(C=O)C=C1 KUCOHFSKRZZVRO-UHFFFAOYSA-N 0.000 description 1
- DZLFLBLQUQXARW-UHFFFAOYSA-N tetrabutylammonium Chemical compound CCCC[N+](CCCC)(CCCC)CCCC DZLFLBLQUQXARW-UHFFFAOYSA-N 0.000 description 1
- CBXCPBUEXACCNR-UHFFFAOYSA-N tetraethylammonium Chemical class CC[N+](CC)(CC)CC CBXCPBUEXACCNR-UHFFFAOYSA-N 0.000 description 1
- 229940073455 tetraethylammonium hydroxide Drugs 0.000 description 1
- LRGJRHZIDJQFCL-UHFFFAOYSA-M tetraethylazanium;hydroxide Chemical compound [OH-].CC[N+](CC)(CC)CC LRGJRHZIDJQFCL-UHFFFAOYSA-M 0.000 description 1
- ZJKOMXZUJBYOOK-UHFFFAOYSA-M tetraphenylazanium;hydroxide Chemical compound [OH-].C1=CC=CC=C1[N+](C=1C=CC=CC=1)(C=1C=CC=CC=1)C1=CC=CC=C1 ZJKOMXZUJBYOOK-UHFFFAOYSA-M 0.000 description 1
- LPSKDVINWQNWFE-UHFFFAOYSA-M tetrapropylazanium;hydroxide Chemical compound [OH-].CCC[N+](CCC)(CCC)CCC LPSKDVINWQNWFE-UHFFFAOYSA-M 0.000 description 1
- 229920002725 thermoplastic elastomer Polymers 0.000 description 1
- 229920005992 thermoplastic resin Polymers 0.000 description 1
- 239000005439 thermosphere Substances 0.000 description 1
- 125000005270 trialkylamine group Chemical group 0.000 description 1
- STCOOQWBFONSKY-UHFFFAOYSA-N tributyl phosphate Chemical compound CCCCOP(=O)(OCCCC)OCCCC STCOOQWBFONSKY-UHFFFAOYSA-N 0.000 description 1
- FSZYUEKEGFLFPC-UHFFFAOYSA-M tributyl(phenyl)azanium;hydroxide Chemical compound [OH-].CCCC[N+](CCCC)(CCCC)C1=CC=CC=C1 FSZYUEKEGFLFPC-UHFFFAOYSA-M 0.000 description 1
- DQWPFSLDHJDLRL-UHFFFAOYSA-N triethyl phosphate Chemical compound CCOP(=O)(OCC)OCC DQWPFSLDHJDLRL-UHFFFAOYSA-N 0.000 description 1
- GPHXJBZAVNFMKX-UHFFFAOYSA-M triethyl(phenyl)azanium;hydroxide Chemical compound [OH-].CC[N+](CC)(CC)C1=CC=CC=C1 GPHXJBZAVNFMKX-UHFFFAOYSA-M 0.000 description 1
- RXJKFRMDXUJTEX-UHFFFAOYSA-N triethylphosphine Chemical compound CCP(CC)CC RXJKFRMDXUJTEX-UHFFFAOYSA-N 0.000 description 1
- IGNTWNVBGLNYDV-UHFFFAOYSA-N triisopropylphosphine Chemical compound CC(C)P(C(C)C)C(C)C IGNTWNVBGLNYDV-UHFFFAOYSA-N 0.000 description 1
- CYTQBVOFDCPGCX-UHFFFAOYSA-N trimethyl phosphite Chemical compound COP(OC)OC CYTQBVOFDCPGCX-UHFFFAOYSA-N 0.000 description 1
- HADKRTWCOYPCPH-UHFFFAOYSA-M trimethylphenylammonium hydroxide Chemical compound [OH-].C[N+](C)(C)C1=CC=CC=C1 HADKRTWCOYPCPH-UHFFFAOYSA-M 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
- 239000002966 varnish Substances 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 238000004260 weight control Methods 0.000 description 1
- 239000010456 wollastonite Substances 0.000 description 1
- 229910052882 wollastonite Inorganic materials 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
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/32—Phosphorus-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
- C08K5/00—Use of organic ingredients
- C08K5/02—Halogenated hydrocarbons
-
- 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
- C08K5/36—Sulfur-, selenium-, or tellurium-containing compounds
- C08K5/41—Compounds containing sulfur bound to oxygen
- C08K5/42—Sulfonic acids; Derivatives thereof
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29K—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
- B29K2069/00—Use of PC, i.e. polycarbonates or derivatives thereof, as moulding material
-
- 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
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- 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)
- Manufacture Of Macromolecular Shaped Articles (AREA)
- Injection Moulding Of Plastics Or The Like (AREA)
- Polyesters Or Polycarbonates (AREA)
Abstract
Description
Claims (30)
Applications Claiming Priority (9)
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JP2010-083181 | 2010-03-31 | ||
JP2010083181 | 2010-03-31 | ||
JP2010-262054 | 2010-11-25 | ||
JP2010-262057 | 2010-11-25 | ||
JP2010262054 | 2010-11-25 | ||
JP2010262057 | 2010-11-25 | ||
JP2010262053 | 2010-11-25 | ||
JP2010-262053 | 2010-11-25 | ||
PCT/JP2011/058326 WO2011125896A1 (ja) | 2010-03-31 | 2011-03-31 | ポリカーボネート樹脂組成物、その製造方法及び同樹脂組成物の成形体 |
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CN102822276A true CN102822276A (zh) | 2012-12-12 |
CN102822276B CN102822276B (zh) | 2015-10-14 |
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CN201180016601.6A Active CN102822276B (zh) | 2010-03-31 | 2011-03-31 | 聚碳酸酯树脂组合物、其制造方法以及该树脂组合物的成型体 |
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US (1) | US9777152B2 (zh) |
EP (1) | EP2557123B1 (zh) |
KR (1) | KR101455487B1 (zh) |
CN (1) | CN102822276B (zh) |
TW (1) | TWI494368B (zh) |
WO (1) | WO2011125896A1 (zh) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN103897165A (zh) * | 2012-12-27 | 2014-07-02 | 第一毛织株式会社 | 共聚聚碳酸酯树脂、制备其的方法及包含其的制品 |
CN111108151A (zh) * | 2017-10-17 | 2020-05-05 | 三菱工程塑料株式会社 | 树脂组合物和成型品 |
CN112969758A (zh) * | 2018-11-08 | 2021-06-15 | 三菱工程塑料株式会社 | 芳香族聚碳酸酯树脂组合物 |
Families Citing this family (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102822277B (zh) | 2010-03-31 | 2014-08-27 | 三菱化学株式会社 | 聚碳酸酯树脂组合物、其制造方法以及该树脂组合物的成型体 |
JP6207816B2 (ja) | 2011-08-01 | 2017-10-04 | 三菱ケミカル株式会社 | ポリカーボネート樹脂積層体 |
JP6163644B2 (ja) * | 2012-03-30 | 2017-07-19 | 三菱ケミカル株式会社 | ポリカーボネート樹脂及びその組成物 |
JP2013216796A (ja) * | 2012-04-10 | 2013-10-24 | Mitsubishi Chemicals Corp | ポリカーボネート樹脂成形体 |
JP6055655B2 (ja) * | 2012-07-12 | 2016-12-27 | 三菱化学株式会社 | ポリカーボネート樹脂成形品 |
JP6125181B2 (ja) * | 2012-09-05 | 2017-05-10 | 三菱化学株式会社 | ポリカーボネート樹脂組成物 |
WO2016016422A1 (de) * | 2014-08-01 | 2016-02-04 | Covestro Deutschland Ag | Copolycarbonat-zusammensetzungen mit cyclischen und linearen oligomeren und verbesserten rheologischen eigenschaften |
KR102383387B1 (ko) * | 2014-08-01 | 2022-04-07 | 코베스트로 도이칠란트 아게 | 개선된 광학적 성질을 갖는, 시클릭 올리고머 및 선형 올리고머를 갖는 코폴리카르보네이트 조성물 |
JP2017524051A (ja) * | 2014-08-01 | 2017-08-24 | 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 | 分岐構造および環状オリゴマーならびに改善したレオロジー特性を有するコポリカーボネート組成物 |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20030060575A1 (en) * | 2001-07-16 | 2003-03-27 | Caruso Andrew James | Polycarbonates suitable for use in optical articles |
WO2008018467A1 (fr) * | 2006-08-08 | 2008-02-14 | Mitsubishi Gas Chemical Company, Inc. | Corps photosensible électrophotographique |
CN101511937A (zh) * | 2006-07-12 | 2009-08-19 | 沙伯基础创新塑料知识产权有限公司 | 阻燃和耐化学的热塑性聚碳酸酯组合物 |
Family Cites Families (18)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE2248817C2 (de) | 1972-10-05 | 1981-09-24 | Bayer Ag, 5090 Leverkusen | Polycarbonatmischungen |
JPS6210160A (ja) | 1985-07-08 | 1987-01-19 | Idemitsu Kosan Co Ltd | 光学機器用素材 |
JPH0621227B2 (ja) | 1986-08-11 | 1994-03-23 | 日本合成ゴム株式会社 | ポリカ−ボネ−ト樹脂組成物 |
JPS6469625A (en) | 1987-09-10 | 1989-03-15 | Daicel Chem | Polycarbonate polymer having excellent surface hardness |
JPH04279659A (ja) | 1991-03-08 | 1992-10-05 | Asahi Chem Ind Co Ltd | ポリカーボネート樹脂組成物 |
JPH08183852A (ja) | 1994-12-28 | 1996-07-16 | Nippon G Ii Plast Kk | コポリカーボネート、コポリカーボネート組成物およびこれらの製造方法 |
JPH09176473A (ja) | 1995-12-25 | 1997-07-08 | Teijin Chem Ltd | 芳香族ポリカーボネート樹脂組成物 |
EP1287073B1 (en) | 2000-05-01 | 2004-06-02 | General Electric Company | Clear polycarbonate blends |
US6537636B1 (en) * | 2000-06-05 | 2003-03-25 | General Electric Company | Data storage media containing clear polycarbonate blends |
JP2003128906A (ja) | 2001-10-29 | 2003-05-08 | Teijin Chem Ltd | 芳香族ポリカーボネート樹脂組成物および光学用成形品 |
JP4281998B2 (ja) * | 2003-06-06 | 2009-06-17 | 三菱瓦斯化学株式会社 | ポリカーボネート樹脂組成物 |
JP2005272708A (ja) | 2004-03-25 | 2005-10-06 | Fuji Photo Film Co Ltd | 表面処理ポリカーボネート成形品 |
US7700696B2 (en) * | 2006-06-28 | 2010-04-20 | Sabic Innovative Plastics Ip B.V. | Polycarbonate composition having improved scratch resistance, and articles formed therefrom |
US20090176946A1 (en) | 2008-01-03 | 2009-07-09 | Sabic Innovative Plastics Ip B.V. | Polycarbonate blends with high scratch resistance and ductility |
JP5524463B2 (ja) | 2008-09-04 | 2014-06-18 | 帝人株式会社 | ガラス繊維強化難燃性樹脂組成物からなる鏡筒 |
KR101188349B1 (ko) * | 2008-12-17 | 2012-10-05 | 제일모직주식회사 | 투명성 및 내스크래치성이 향상된 폴리카보네이트계 수지 조성물 |
EP2199076B1 (en) * | 2008-12-18 | 2013-02-20 | SABIC Innovative Plastics IP B.V. | Methods for the manufacture of polycarbonate compositions, the compositions formed thereby, and articles thereof |
JP5468896B2 (ja) | 2009-01-22 | 2014-04-09 | 帝人株式会社 | ポリカーボネート樹脂積層体 |
-
2011
- 2011-03-31 CN CN201180016601.6A patent/CN102822276B/zh active Active
- 2011-03-31 WO PCT/JP2011/058326 patent/WO2011125896A1/ja active Application Filing
- 2011-03-31 KR KR1020127025228A patent/KR101455487B1/ko active IP Right Grant
- 2011-03-31 TW TW100111486A patent/TWI494368B/zh active
- 2011-03-31 EP EP11765796.5A patent/EP2557123B1/en active Active
-
2012
- 2012-10-01 US US13/632,957 patent/US9777152B2/en active Active
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20030060575A1 (en) * | 2001-07-16 | 2003-03-27 | Caruso Andrew James | Polycarbonates suitable for use in optical articles |
CN101511937A (zh) * | 2006-07-12 | 2009-08-19 | 沙伯基础创新塑料知识产权有限公司 | 阻燃和耐化学的热塑性聚碳酸酯组合物 |
WO2008018467A1 (fr) * | 2006-08-08 | 2008-02-14 | Mitsubishi Gas Chemical Company, Inc. | Corps photosensible électrophotographique |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN103897165A (zh) * | 2012-12-27 | 2014-07-02 | 第一毛织株式会社 | 共聚聚碳酸酯树脂、制备其的方法及包含其的制品 |
CN103897165B (zh) * | 2012-12-27 | 2016-01-06 | 第一毛织株式会社 | 共聚聚碳酸酯树脂、制备其的方法及包含其的制品 |
CN111108151A (zh) * | 2017-10-17 | 2020-05-05 | 三菱工程塑料株式会社 | 树脂组合物和成型品 |
CN111108151B (zh) * | 2017-10-17 | 2023-06-09 | 三菱工程塑料株式会社 | 树脂组合物和成型品 |
CN112969758A (zh) * | 2018-11-08 | 2021-06-15 | 三菱工程塑料株式会社 | 芳香族聚碳酸酯树脂组合物 |
Also Published As
Publication number | Publication date |
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EP2557123A1 (en) | 2013-02-13 |
US9777152B2 (en) | 2017-10-03 |
KR101455487B1 (ko) | 2014-10-27 |
WO2011125896A1 (ja) | 2011-10-13 |
TWI494368B (zh) | 2015-08-01 |
TW201141943A (en) | 2011-12-01 |
US20130030113A1 (en) | 2013-01-31 |
KR20130024893A (ko) | 2013-03-08 |
CN102822276B (zh) | 2015-10-14 |
EP2557123B1 (en) | 2020-04-29 |
EP2557123A4 (en) | 2013-09-18 |
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