CN100415813C - 阻燃性聚碳酸酯-abs共混物、其制备方法、其用途以及由其得到的模制体 - Google Patents
阻燃性聚碳酸酯-abs共混物、其制备方法、其用途以及由其得到的模制体 Download PDFInfo
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- CN100415813C CN100415813C CNB008146950A CN00814695A CN100415813C CN 100415813 C CN100415813 C CN 100415813C CN B008146950 A CNB008146950 A CN B008146950A CN 00814695 A CN00814695 A CN 00814695A CN 100415813 C CN100415813 C CN 100415813C
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- phosphas
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- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 1
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- 102100028017 Tripartite motif-containing protein 44 Human genes 0.000 description 1
- 238000006887 Ullmann reaction Methods 0.000 description 1
- MCMNRKCIXSYSNV-UHFFFAOYSA-N Zirconium dioxide Chemical class O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 description 1
- OCKWAZCWKSMKNC-UHFFFAOYSA-N [3-octadecanoyloxy-2,2-bis(octadecanoyloxymethyl)propyl] octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(COC(=O)CCCCCCCCCCCCCCCCC)(COC(=O)CCCCCCCCCCCCCCCCC)COC(=O)CCCCCCCCCCCCCCCCC OCKWAZCWKSMKNC-UHFFFAOYSA-N 0.000 description 1
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- 230000008901 benefit Effects 0.000 description 1
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- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
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- 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
- 125000004799 bromophenyl group Chemical group 0.000 description 1
- XZKRXPZXQLARHH-UHFFFAOYSA-N buta-1,3-dienylbenzene Chemical compound C=CC=CC1=CC=CC=C1 XZKRXPZXQLARHH-UHFFFAOYSA-N 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 125000002603 chloroethyl group Chemical group [H]C([*])([H])C([H])([H])Cl 0.000 description 1
- 125000000068 chlorophenyl group Chemical group 0.000 description 1
- YACLQRRMGMJLJV-UHFFFAOYSA-N chloroprene Chemical compound ClC(=C)C=C YACLQRRMGMJLJV-UHFFFAOYSA-N 0.000 description 1
- IJOOHPMOJXWVHK-UHFFFAOYSA-N chlorotrimethylsilane Chemical compound C[Si](C)(C)Cl IJOOHPMOJXWVHK-UHFFFAOYSA-N 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
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- USIUVYZYUHIAEV-UHFFFAOYSA-N diphenyl ether Chemical class C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 description 1
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- 125000004185 ester group Chemical group 0.000 description 1
- QHSJIZLJUFMIFP-UHFFFAOYSA-N ethene;1,1,2,2-tetrafluoroethene Chemical compound C=C.FC(F)=C(F)F QHSJIZLJUFMIFP-UHFFFAOYSA-N 0.000 description 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
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- 239000011737 fluorine Substances 0.000 description 1
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- 235000015203 fruit juice Nutrition 0.000 description 1
- 238000010413 gardening Methods 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 150000002366 halogen compounds Chemical class 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- HCDGVLDPFQMKDK-UHFFFAOYSA-N hexafluoropropylene Chemical group FC(F)=C(F)C(F)(F)F HCDGVLDPFQMKDK-UHFFFAOYSA-N 0.000 description 1
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- 150000002430 hydrocarbons Chemical class 0.000 description 1
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- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
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- 229910052749 magnesium Inorganic materials 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 1
- OJURWUUOVGOHJZ-UHFFFAOYSA-N methyl 2-[(2-acetyloxyphenyl)methyl-[2-[(2-acetyloxyphenyl)methyl-(2-methoxy-2-oxoethyl)amino]ethyl]amino]acetate Chemical compound C=1C=CC=C(OC(C)=O)C=1CN(CC(=O)OC)CCN(CC(=O)OC)CC1=CC=CC=C1OC(C)=O OJURWUUOVGOHJZ-UHFFFAOYSA-N 0.000 description 1
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- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 1
- 229910017464 nitrogen compound Inorganic materials 0.000 description 1
- 150000002830 nitrogen compounds Chemical class 0.000 description 1
- 150000002896 organic halogen compounds Chemical class 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- PQQKPALAQIIWST-UHFFFAOYSA-N oxomolybdenum Chemical class [Mo]=O PQQKPALAQIIWST-UHFFFAOYSA-N 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 229920002866 paraformaldehyde Polymers 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- 229940059574 pentaerithrityl Drugs 0.000 description 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 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
- 239000010452 phosphate Substances 0.000 description 1
- VXTFGYMINLXJPW-UHFFFAOYSA-N phosphinane Chemical compound C1CCPCC1 VXTFGYMINLXJPW-UHFFFAOYSA-N 0.000 description 1
- 150000003014 phosphoric acid esters Chemical class 0.000 description 1
- 150000003018 phosphorus compounds Chemical class 0.000 description 1
- 238000006068 polycondensation reaction Methods 0.000 description 1
- 125000003367 polycyclic group Chemical group 0.000 description 1
- 239000001205 polyphosphate Substances 0.000 description 1
- 235000011176 polyphosphates Nutrition 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
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- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 229920002981 polyvinylidene fluoride Chemical group 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 229920005604 random copolymer Polymers 0.000 description 1
- 239000003340 retarding agent Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000000377 silicon dioxide Chemical class 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 229960001866 silicon dioxide Drugs 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
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- 238000005507 spraying Methods 0.000 description 1
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- 150000003462 sulfoxides Chemical class 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- 239000000454 talc Chemical class 0.000 description 1
- 235000012222 talc Nutrition 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- WYXIGTJNYDDFFH-UHFFFAOYSA-Q triazanium;borate Chemical class [NH4+].[NH4+].[NH4+].[O-]B([O-])[O-] WYXIGTJNYDDFFH-UHFFFAOYSA-Q 0.000 description 1
- 125000003258 trimethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])[*:1] 0.000 description 1
- QXJQHYBHAIHNGG-UHFFFAOYSA-N trimethylolethane Chemical compound OCC(C)(CO)CO QXJQHYBHAIHNGG-UHFFFAOYSA-N 0.000 description 1
- BIKXLKXABVUSMH-UHFFFAOYSA-N trizinc;diborate Chemical class [Zn+2].[Zn+2].[Zn+2].[O-]B([O-])[O-].[O-]B([O-])[O-] BIKXLKXABVUSMH-UHFFFAOYSA-N 0.000 description 1
- 238000009423 ventilation Methods 0.000 description 1
- 230000003245 working effect Effects 0.000 description 1
- 125000005023 xylyl group Chemical group 0.000 description 1
- JLYXXMFPNIAWKQ-UHFFFAOYSA-N γ Benzene hexachloride Chemical compound ClC1C(Cl)C(Cl)C(Cl)C(Cl)C1Cl JLYXXMFPNIAWKQ-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K21/00—Fireproofing materials
- C09K21/14—Macromolecular materials
-
- 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
- C08K5/49—Phosphorus-containing compounds
- C08K5/51—Phosphorus bound to oxygen
- C08K5/53—Phosphorus bound to oxygen bound to oxygen and to carbon only
- C08K5/5317—Phosphonic compounds, e.g. R—P(:O)(OR')2
- C08K5/5333—Esters of phosphonic acids
- C08K5/5353—Esters of phosphonic acids containing also nitrogen
-
- 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
- C08L69/00—Compositions of polycarbonates; Compositions of derivatives of polycarbonates
- C08L69/005—Polyester-carbonates
-
- 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
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Processes Of Treating Macromolecular Substances (AREA)
- Graft Or Block Polymers (AREA)
- Polyesters Or Polycarbonates (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19941821A DE19941821A1 (de) | 1999-09-02 | 1999-09-02 | Flammwidrige Polycarbonat-ABS-Blends |
| DE19941821.7 | 1999-09-02 |
Publications (2)
| Publication Number | Publication Date |
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| CN1382181A CN1382181A (zh) | 2002-11-27 |
| CN100415813C true CN100415813C (zh) | 2008-09-03 |
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CNB008146950A Expired - Fee Related CN100415813C (zh) | 1999-09-02 | 2000-08-22 | 阻燃性聚碳酸酯-abs共混物、其制备方法、其用途以及由其得到的模制体 |
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| Country | Link |
|---|---|
| US (1) | US6528561B1 (enExample) |
| EP (1) | EP1228136B1 (enExample) |
| JP (1) | JP2003524027A (enExample) |
| KR (1) | KR100648581B1 (enExample) |
| CN (1) | CN100415813C (enExample) |
| AR (1) | AR025416A1 (enExample) |
| AT (1) | ATE248888T1 (enExample) |
| AU (1) | AU7278700A (enExample) |
| BR (1) | BR0013759A (enExample) |
| CA (1) | CA2383648A1 (enExample) |
| DE (2) | DE19941821A1 (enExample) |
| DK (1) | DK1228136T3 (enExample) |
| ES (1) | ES2200926T3 (enExample) |
| MX (1) | MXPA02002293A (enExample) |
| MY (1) | MY133630A (enExample) |
| RU (1) | RU2002108179A (enExample) |
| TW (1) | TW585888B (enExample) |
| WO (1) | WO2001018105A1 (enExample) |
Families Citing this family (52)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE19941823A1 (de) * | 1999-09-02 | 2001-03-08 | Bayer Ag | Flammwidrige Polycarbonat-Blends |
| DE19941826A1 (de) * | 1999-09-02 | 2001-03-08 | Bayer Ag | Flammwidrige Polycarbonat-Formmassen |
| DE19941827A1 (de) * | 1999-09-02 | 2001-03-08 | Bayer Ag | Flammwidrige Polycarbonat-Blends |
| DE10152318A1 (de) * | 2001-10-26 | 2003-05-08 | Bayer Ag | Schlagzähmodifizierte flammwidrig ausgerüstete Polycarbonat-Formmassen |
| DE10234419A1 (de) * | 2002-07-29 | 2004-02-12 | Bayer Ag | Flammwidrige Formmassen |
| KR100650910B1 (ko) * | 2004-10-13 | 2006-11-27 | 제일모직주식회사 | 난연성 열가소성 수지 조성물 |
| US7446144B2 (en) * | 2005-09-14 | 2008-11-04 | Bayer Materialscience Llc | Thermoplastic molding composition and articles thermoformed therefrom |
| WO2007078083A1 (en) * | 2005-12-30 | 2007-07-12 | Cheil Industries Inc. | Flame retardant polycarbonate thermoplastic resin composition having good extrusion moldability and impact resistance |
| KR100722149B1 (ko) * | 2005-12-30 | 2007-05-28 | 제일모직주식회사 | 압출가공성 및 내충격성이 우수한 난연성 폴리카보네이트계열가소성 수지 조성물 |
| DE102008015124A1 (de) | 2007-05-16 | 2008-11-20 | Bayer Materialscience Ag | Schlagzähmodifizierte Polycarbonat-Zusammensetzungen |
| DE102007052783A1 (de) * | 2007-11-02 | 2009-05-07 | Bayer Materialscience Ag | Flammwidrige Polycarbonate mit Polyolen |
| KR100877291B1 (ko) * | 2007-11-19 | 2009-01-07 | 제일모직주식회사 | 비할로겐계 난연성 폴리카보네이트계 수지 조성물 |
| KR101004040B1 (ko) * | 2007-12-18 | 2010-12-31 | 제일모직주식회사 | 상용성이 향상된 난연 내스크래치 열가소성 수지 조성물 |
| KR100885819B1 (ko) * | 2007-12-18 | 2009-02-26 | 제일모직주식회사 | 굴절률이 우수한 분지형 아크릴계 공중합체 및 그 제조방법 |
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- 1999-09-02 DE DE19941821A patent/DE19941821A1/de not_active Withdrawn
-
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- 2000-08-22 US US10/069,660 patent/US6528561B1/en not_active Expired - Fee Related
- 2000-08-22 DE DE50003581T patent/DE50003581D1/de not_active Expired - Lifetime
- 2000-08-22 MX MXPA02002293A patent/MXPA02002293A/es not_active Application Discontinuation
- 2000-08-22 KR KR1020027002695A patent/KR100648581B1/ko not_active Expired - Fee Related
- 2000-08-22 WO PCT/EP2000/008163 patent/WO2001018105A1/de not_active Ceased
- 2000-08-22 DK DK00960503T patent/DK1228136T3/da active
- 2000-08-22 CN CNB008146950A patent/CN100415813C/zh not_active Expired - Fee Related
- 2000-08-22 RU RU2002108179/04A patent/RU2002108179A/ru not_active Application Discontinuation
- 2000-08-22 ES ES00960503T patent/ES2200926T3/es not_active Expired - Lifetime
- 2000-08-22 CA CA002383648A patent/CA2383648A1/en not_active Abandoned
- 2000-08-22 BR BR0013759-6A patent/BR0013759A/pt not_active IP Right Cessation
- 2000-08-22 JP JP2001522323A patent/JP2003524027A/ja active Pending
- 2000-08-22 AU AU72787/00A patent/AU7278700A/en not_active Abandoned
- 2000-08-22 AT AT00960503T patent/ATE248888T1/de not_active IP Right Cessation
- 2000-08-22 EP EP00960503A patent/EP1228136B1/de not_active Expired - Lifetime
- 2000-08-28 AR ARP000104464A patent/AR025416A1/es unknown
- 2000-08-28 TW TW089117315A patent/TW585888B/zh not_active IP Right Cessation
- 2000-08-30 MY MYPI20004011 patent/MY133630A/en unknown
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Also Published As
| Publication number | Publication date |
|---|---|
| CA2383648A1 (en) | 2001-03-15 |
| DE19941821A1 (de) | 2001-03-08 |
| JP2003524027A (ja) | 2003-08-12 |
| BR0013759A (pt) | 2002-05-14 |
| TW585888B (en) | 2004-05-01 |
| ATE248888T1 (de) | 2003-09-15 |
| KR100648581B1 (ko) | 2006-11-24 |
| WO2001018105A1 (de) | 2001-03-15 |
| AU7278700A (en) | 2001-04-10 |
| CN1382181A (zh) | 2002-11-27 |
| EP1228136B1 (de) | 2003-09-03 |
| AR025416A1 (es) | 2002-11-27 |
| EP1228136A1 (de) | 2002-08-07 |
| MXPA02002293A (es) | 2002-08-12 |
| RU2002108179A (ru) | 2003-11-10 |
| DK1228136T3 (da) | 2003-11-24 |
| DE50003581D1 (de) | 2003-10-09 |
| KR20020029393A (ko) | 2002-04-18 |
| US6528561B1 (en) | 2003-03-04 |
| MY133630A (en) | 2007-11-30 |
| ES2200926T3 (es) | 2004-03-16 |
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