CN1210340C - 耐γ射线的聚碳酸酯组合物 - Google Patents
耐γ射线的聚碳酸酯组合物 Download PDFInfo
- Publication number
- CN1210340C CN1210340C CNB018074340A CN01807434A CN1210340C CN 1210340 C CN1210340 C CN 1210340C CN B018074340 A CNB018074340 A CN B018074340A CN 01807434 A CN01807434 A CN 01807434A CN 1210340 C CN1210340 C CN 1210340C
- Authority
- CN
- China
- Prior art keywords
- asccharin
- hydroxyphenyl
- compound
- thermoplastic composition
- dimethyl
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
Links
- 229920000515 polycarbonate Polymers 0.000 title claims abstract description 32
- 239000000203 mixture Substances 0.000 title claims abstract description 28
- 239000004417 polycarbonate Substances 0.000 title claims abstract description 27
- 230000005855 radiation Effects 0.000 title abstract description 5
- 150000001875 compounds Chemical class 0.000 claims abstract description 29
- 229920001169 thermoplastic Polymers 0.000 claims abstract description 14
- 239000004416 thermosoftening plastic Substances 0.000 claims abstract description 14
- -1 saccharine compound Chemical class 0.000 claims abstract description 9
- 125000006615 aromatic heterocyclic group Chemical group 0.000 claims abstract description 3
- 125000002837 carbocyclic group Chemical group 0.000 claims abstract description 3
- 239000001257 hydrogen Substances 0.000 claims abstract description 3
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 3
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims abstract description 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract description 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract description 3
- 239000001294 propane Substances 0.000 claims description 13
- 229910052799 carbon Inorganic materials 0.000 claims description 10
- 239000004431 polycarbonate resin Substances 0.000 claims description 9
- 229920005668 polycarbonate resin Polymers 0.000 claims description 9
- 125000004432 carbon atom Chemical group C* 0.000 claims description 8
- 239000011347 resin Substances 0.000 claims description 8
- 229920005989 resin Polymers 0.000 claims description 8
- 125000000217 alkyl group Chemical group 0.000 claims description 4
- 125000001118 alkylidene group Chemical group 0.000 claims description 4
- 125000003118 aryl group Chemical group 0.000 claims description 3
- DEQUKPCANKRTPZ-UHFFFAOYSA-N (2,3-dihydroxyphenyl)-phenylmethanone Chemical compound OC1=CC=CC(C(=O)C=2C=CC=CC=2)=C1O DEQUKPCANKRTPZ-UHFFFAOYSA-N 0.000 claims description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 2
- 125000005466 alkylenyl group Chemical group 0.000 claims description 2
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 2
- 125000004122 cyclic group Chemical group 0.000 claims description 2
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 2
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 2
- KLSLBUSXWBJMEC-UHFFFAOYSA-N 4-Propylphenol Chemical compound CCCC1=CC=C(O)C=C1 KLSLBUSXWBJMEC-UHFFFAOYSA-N 0.000 claims 1
- 229920001519 homopolymer Polymers 0.000 claims 1
- 238000000465 moulding Methods 0.000 abstract description 3
- 239000000654 additive Substances 0.000 abstract description 2
- 238000004519 manufacturing process Methods 0.000 abstract description 2
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 1
- 230000000996 additive effect Effects 0.000 abstract 1
- 125000004957 naphthylene group Chemical group 0.000 abstract 1
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 abstract 1
- 230000000087 stabilizing effect Effects 0.000 abstract 1
- 238000004383 yellowing Methods 0.000 abstract 1
- 238000000034 method Methods 0.000 description 9
- 229930185605 Bisphenol Natural products 0.000 description 6
- 239000004425 Makrolon Substances 0.000 description 5
- 238000005516 engineering process Methods 0.000 description 5
- 238000012360 testing method Methods 0.000 description 5
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 4
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 4
- MNAHQWDCXOHBHK-UHFFFAOYSA-N 1-phenylpropane-1,1-diol Chemical compound CCC(O)(O)C1=CC=CC=C1 MNAHQWDCXOHBHK-UHFFFAOYSA-N 0.000 description 3
- 230000005251 gamma ray Effects 0.000 description 3
- 239000011368 organic material Substances 0.000 description 3
- 239000003381 stabilizer Substances 0.000 description 3
- IANQTJSKSUMEQM-UHFFFAOYSA-N 1-benzofuran Chemical compound C1=CC=C2OC=CC2=C1 IANQTJSKSUMEQM-UHFFFAOYSA-N 0.000 description 2
- ACZGCWSMSTYWDQ-UHFFFAOYSA-N 3h-1-benzofuran-2-one Chemical group C1=CC=C2OC(=O)CC2=C1 ACZGCWSMSTYWDQ-UHFFFAOYSA-N 0.000 description 2
- OIFBSDVPJOWBCH-UHFFFAOYSA-N Diethyl carbonate Chemical compound CCOC(=O)OCC OIFBSDVPJOWBCH-UHFFFAOYSA-N 0.000 description 2
- XYFCBTPGUUZFHI-UHFFFAOYSA-N Phosphine Chemical compound P XYFCBTPGUUZFHI-UHFFFAOYSA-N 0.000 description 2
- 150000001408 amides Chemical class 0.000 description 2
- UHOVQNZJYSORNB-UHFFFAOYSA-N benzene Substances C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 2
- QMKYBPDZANOJGF-UHFFFAOYSA-N benzene-1,3,5-tricarboxylic acid Chemical compound OC(=O)C1=CC(C(O)=O)=CC(C(O)=O)=C1 QMKYBPDZANOJGF-UHFFFAOYSA-N 0.000 description 2
- 238000009833 condensation Methods 0.000 description 2
- 230000005494 condensation Effects 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 2
- 150000002500 ions Chemical class 0.000 description 2
- KJFMBFZCATUALV-UHFFFAOYSA-N phenolphthalein Chemical compound C1=CC(O)=CC=C1C1(C=2C=CC(O)=CC=2)C2=CC=CC=C2C(=O)O1 KJFMBFZCATUALV-UHFFFAOYSA-N 0.000 description 2
- 238000006068 polycondensation reaction Methods 0.000 description 2
- 229920005862 polyol Polymers 0.000 description 2
- 150000003077 polyols Chemical class 0.000 description 2
- UIAFKZKHHVMJGS-UHFFFAOYSA-N 2,4-dihydroxybenzoic acid Chemical compound OC(=O)C1=CC=C(O)C=C1O UIAFKZKHHVMJGS-UHFFFAOYSA-N 0.000 description 1
- NANGQJICIOUURV-UHFFFAOYSA-N 3-phenyl-3h-1-benzofuran-2-one Chemical class O=C1OC2=CC=CC=C2C1C1=CC=CC=C1 NANGQJICIOUURV-UHFFFAOYSA-N 0.000 description 1
- VPWNQTHUCYMVMZ-UHFFFAOYSA-N 4,4'-sulfonyldiphenol Chemical class C1=CC(O)=CC=C1S(=O)(=O)C1=CC=C(O)C=C1 VPWNQTHUCYMVMZ-UHFFFAOYSA-N 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- 239000004262 Ethyl gallate Substances 0.000 description 1
- 101000648997 Homo sapiens Tripartite motif-containing protein 44 Proteins 0.000 description 1
- 238000012696 Interfacial polycondensation Methods 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- JPYHHZQJCSQRJY-UHFFFAOYSA-N Phloroglucinol Natural products CCC=CCC=CCC=CCC=CCCCCC(=O)C1=C(O)C=C(O)C=C1O JPYHHZQJCSQRJY-UHFFFAOYSA-N 0.000 description 1
- YGYAWVDWMABLBF-UHFFFAOYSA-N Phosgene Chemical compound ClC(Cl)=O YGYAWVDWMABLBF-UHFFFAOYSA-N 0.000 description 1
- 239000004902 Softening Agent Substances 0.000 description 1
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 1
- 102100028017 Tripartite motif-containing protein 44 Human genes 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- 235000006708 antioxidants Nutrition 0.000 description 1
- 235000010290 biphenyl Nutrition 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 238000012512 characterization method Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- MGNCLNQXLYJVJD-UHFFFAOYSA-N cyanuric chloride Chemical compound ClC1=NC(Cl)=NC(Cl)=N1 MGNCLNQXLYJVJD-UHFFFAOYSA-N 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 239000000645 desinfectant Substances 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N ferric oxide Chemical compound O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 230000004927 fusion Effects 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 230000001939 inductive effect Effects 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 238000001746 injection moulding Methods 0.000 description 1
- 125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 239000003595 mist Substances 0.000 description 1
- 229920000620 organic polymer Polymers 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 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
- XRBCRPZXSCBRTK-UHFFFAOYSA-N phosphonous acid Chemical compound OPO XRBCRPZXSCBRTK-UHFFFAOYSA-N 0.000 description 1
- OJMIONKXNSYLSR-UHFFFAOYSA-N phosphorous acid Chemical compound OP(O)O OJMIONKXNSYLSR-UHFFFAOYSA-N 0.000 description 1
- 229910000073 phosphorus hydride Inorganic materials 0.000 description 1
- 239000002861 polymer material Substances 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000010189 synthetic method Methods 0.000 description 1
- 229920001897 terpolymer Polymers 0.000 description 1
- 239000012745 toughening agent Substances 0.000 description 1
- 238000005809 transesterification reaction Methods 0.000 description 1
Classifications
-
- 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
- C08K5/15—Heterocyclic compounds having oxygen in the ring
- C08K5/151—Heterocyclic compounds having oxygen in the ring having one oxygen atom in the ring
- C08K5/1535—Five-membered rings
-
- 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
- C08K5/15—Heterocyclic compounds having oxygen in the ring
-
- 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
- C08K5/45—Heterocyclic compounds having sulfur in the ring
- C08K5/46—Heterocyclic compounds having sulfur in the ring with oxygen or nitrogen in the ring
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)
- Materials For Medical Uses (AREA)
- Manufacture Of Macromolecular Shaped Articles (AREA)
- Macromonomer-Based Addition Polymer (AREA)
Abstract
Description
3兆雷曝露组分 | 实施例1 | 实施例2 | 实施例3 | 实施例4 | 实施例5 | 实施例6 |
聚碳酸酯,wt% | 100 | 99.5 | 99.5 | 99.5 | 99.5 | 99.25 |
稳定剂,wt% | 0 | 0.5 | 0 | 0.25 | 0.5 | 0.25 |
稳定剂II,wt% | 0 | 0 | 0.5 | 0.25 | 0.25 | 0.5 |
YI0 | 4.2 | 4.2 | 3.6 | 4.6 | 6.0 | 7.4 |
YI10 | 28.2 | 22.8 | 19.6 | 20.0 | 20.2 | 15.5 |
ΔYI | 24.00 | 18.6 | 16.0 | 15.4 | 14.2 | 8.1 |
5兆雷曝露组分 | 实施例1 | 实施例2 | 实施例3 | 实施例4 | 实施例5 | 实施例6 |
聚碳酸酯,wt% | 100 | 99.5 | 99.5 | 99.5 | 99.5 | 99.5 |
稳定剂,wt% | 0 | 0.5 | 0 | 0.25 | 0.5 | 0.25 |
稳定剂II,wt% | 0 | 0 | 0.5 | 0.25 | 0.25 | 0.5 |
YI0 | 4.2 | 4.2 | 3.6 | 4.6 | 6.0 | 7.4 |
YI10 | 51.9 | 35.8 | 36.0 | 35.0 | 31.8 | 30.0 |
ΔYI | 47.7 | 31.6 | 32.4 | 30.6 | 25.8 | 22.6 |
Claims (10)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US09/541,570 | 2000-04-03 | ||
US09/541,570 US6197854B1 (en) | 2000-04-03 | 2000-04-03 | Polycarbonate composition resistant to gamma radiation |
Publications (2)
Publication Number | Publication Date |
---|---|
CN1420906A CN1420906A (zh) | 2003-05-28 |
CN1210340C true CN1210340C (zh) | 2005-07-13 |
Family
ID=24160145
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CNB018074340A Expired - Fee Related CN1210340C (zh) | 2000-04-03 | 2001-03-30 | 耐γ射线的聚碳酸酯组合物 |
Country Status (13)
Country | Link |
---|---|
US (1) | US6197854B1 (zh) |
EP (1) | EP1274781B1 (zh) |
JP (1) | JP4801308B2 (zh) |
KR (1) | KR20020086753A (zh) |
CN (1) | CN1210340C (zh) |
AT (1) | ATE284920T1 (zh) |
AU (1) | AU2001253102A1 (zh) |
BR (1) | BR0109775A (zh) |
CA (1) | CA2404524A1 (zh) |
DE (1) | DE60107830T2 (zh) |
ES (1) | ES2233626T3 (zh) |
TW (1) | TWI225503B (zh) |
WO (1) | WO2001074934A2 (zh) |
Families Citing this family (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CA2378922C (en) * | 2002-01-16 | 2009-01-27 | Rutgers, The State University Of New Jersey | Compositions and methods of making plastic articles from polymer blends containing polyethylene |
US7078447B2 (en) * | 2003-11-21 | 2006-07-18 | General Electric Company | Ionizing radiation stable polyarylestercarbonate compositions |
DE10360367A1 (de) * | 2003-12-22 | 2005-07-21 | Bayer Materialscience Ag | Stabilisierte thermoplastische Zusammensetzungen |
US7511092B2 (en) * | 2005-10-07 | 2009-03-31 | Sabic Innovative Plastics Ip B.V. | Stabilized thermoplastic composition, method of making, and articles formed therefrom |
US7528212B2 (en) * | 2005-11-18 | 2009-05-05 | Sabic Innovative Plastics Ip B.V. | Ionizing radiation stable thermoplastic composition, method of making, and articles formed therefrom |
US20070232953A1 (en) * | 2006-03-31 | 2007-10-04 | Ethicon Endo-Surgery, Inc. | MRI biopsy device |
US7655723B2 (en) * | 2007-05-02 | 2010-02-02 | Fina Technology, Inc. | Radiation resistant polypropylene materials |
JP6106380B2 (ja) * | 2012-08-14 | 2017-03-29 | 東洋製罐グループホールディングス株式会社 | 抗菌性マスターバッチ及びそれを用いた成形体 |
Family Cites Families (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2042562B (en) | 1979-02-05 | 1983-05-11 | Sandoz Ltd | Stabilising polymers |
US4624972A (en) | 1985-11-25 | 1986-11-25 | The Dow Chemical Company | Gamma radiation resistant carbonate polymer compositions |
US5187211A (en) | 1987-06-26 | 1993-02-16 | Miles Inc. | Gamma radiation resistant polycarbonate compositions |
US4804692A (en) | 1987-11-09 | 1989-02-14 | Mobay Corporation | Gamma-radiation resistant polycarbonate compositions |
US4963598A (en) | 1988-04-18 | 1990-10-16 | Mobay Corporation | Gamma radiation resistant polycarbonate compositions |
US4874802A (en) | 1988-06-16 | 1989-10-17 | Mobay Corporation | Polycarbonate compositions resistant to gamma radiation |
US5006572A (en) | 1989-01-24 | 1991-04-09 | Mobay Corporation | Gamma radiation resistant polycarbonate composition |
US5175312A (en) | 1989-08-31 | 1992-12-29 | Ciba-Geigy Corporation | 3-phenylbenzofuran-2-ones |
DE4132629A1 (de) | 1991-10-01 | 1993-04-08 | Bayer Ag | Verwendung von kern-aromatischen sulfonsaeureestern zur stabilisierung von thermoplastischen polycarbonaten gegen einwirkung von gammastrahlen |
US5187208A (en) | 1991-11-06 | 1993-02-16 | Miles Inc. | Polycarbonate compositions resistant to gamma radiation |
US5214078A (en) | 1992-06-03 | 1993-05-25 | Miles Inc. | Gamma radiation resistant polycarbonate composition |
TW284762B (zh) | 1993-09-17 | 1996-09-01 | Ciba Geigy Ag | |
DE19516787A1 (de) * | 1995-05-08 | 1996-11-14 | Bayer Ag | Gegen Gamma-Strahlung stabilisierte (Co)Polycarbonate |
ES2149678B1 (es) * | 1997-03-06 | 2001-05-16 | Ciba Sc Holding Ag | Estabilizacion de policarbonatos, poliesteres y policetonas. |
DE19726195A1 (de) * | 1997-06-20 | 1998-12-24 | Bayer Ag | Verwendung von Saccharin zur Stabilisierung von thermoplastischen, aromatischen Polycarbonaten |
-
2000
- 2000-04-03 US US09/541,570 patent/US6197854B1/en not_active Expired - Lifetime
-
2001
- 2001-03-20 TW TW090106396A patent/TWI225503B/zh not_active IP Right Cessation
- 2001-03-30 WO PCT/US2001/010745 patent/WO2001074934A2/en active IP Right Grant
- 2001-03-30 ES ES01926574T patent/ES2233626T3/es not_active Expired - Lifetime
- 2001-03-30 BR BR0109775-0A patent/BR0109775A/pt not_active IP Right Cessation
- 2001-03-30 CA CA002404524A patent/CA2404524A1/en not_active Abandoned
- 2001-03-30 AT AT01926574T patent/ATE284920T1/de not_active IP Right Cessation
- 2001-03-30 AU AU2001253102A patent/AU2001253102A1/en not_active Abandoned
- 2001-03-30 KR KR1020027013194A patent/KR20020086753A/ko active IP Right Grant
- 2001-03-30 CN CNB018074340A patent/CN1210340C/zh not_active Expired - Fee Related
- 2001-03-30 JP JP2001572616A patent/JP4801308B2/ja not_active Expired - Fee Related
- 2001-03-30 DE DE60107830T patent/DE60107830T2/de not_active Expired - Lifetime
- 2001-03-30 EP EP01926574A patent/EP1274781B1/en not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
EP1274781B1 (en) | 2004-12-15 |
WO2001074934A2 (en) | 2001-10-11 |
ES2233626T3 (es) | 2005-06-16 |
DE60107830D1 (de) | 2005-01-20 |
CN1420906A (zh) | 2003-05-28 |
CA2404524A1 (en) | 2001-10-11 |
JP4801308B2 (ja) | 2011-10-26 |
BR0109775A (pt) | 2003-01-21 |
JP2003529652A (ja) | 2003-10-07 |
DE60107830T2 (de) | 2006-02-09 |
US6197854B1 (en) | 2001-03-06 |
EP1274781A2 (en) | 2003-01-15 |
AU2001253102A1 (en) | 2001-10-15 |
ATE284920T1 (de) | 2005-01-15 |
TWI225503B (en) | 2004-12-21 |
WO2001074934A3 (en) | 2002-03-21 |
KR20020086753A (ko) | 2002-11-18 |
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