WO2009072846A2 - Composition de résine de polycarbonate ignifuge dotée d'une transmission infrarouge élevée - Google Patents
Composition de résine de polycarbonate ignifuge dotée d'une transmission infrarouge élevée Download PDFInfo
- Publication number
- WO2009072846A2 WO2009072846A2 PCT/KR2008/007229 KR2008007229W WO2009072846A2 WO 2009072846 A2 WO2009072846 A2 WO 2009072846A2 KR 2008007229 W KR2008007229 W KR 2008007229W WO 2009072846 A2 WO2009072846 A2 WO 2009072846A2
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- weight
- composition according
- fluoroolefin
- aromatic
- polycarbonate resin
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 24
- 229920005668 polycarbonate resin Polymers 0.000 title claims abstract description 17
- 239000004431 polycarbonate resin Substances 0.000 title claims abstract description 17
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 title claims description 9
- 239000003063 flame retardant Substances 0.000 title claims description 9
- 230000005540 biological transmission Effects 0.000 title description 2
- 125000003118 aryl group Chemical group 0.000 claims abstract description 33
- 229910019142 PO4 Inorganic materials 0.000 claims abstract description 27
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 claims abstract description 27
- 239000010452 phosphate Substances 0.000 claims abstract description 27
- 239000011342 resin composition Substances 0.000 claims abstract description 14
- -1 aromatic monophosphate Chemical class 0.000 claims description 11
- 229910052736 halogen Inorganic materials 0.000 claims description 9
- 150000001875 compounds Chemical class 0.000 claims description 8
- 239000011368 organic material Substances 0.000 claims description 8
- 150000002367 halogens Chemical class 0.000 claims description 7
- 229920005992 thermoplastic resin Polymers 0.000 claims description 6
- 239000004698 Polyethylene Substances 0.000 claims description 4
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical group C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 claims description 4
- 239000001177 diphosphate Substances 0.000 claims description 4
- XPPKVPWEQAFLFU-UHFFFAOYSA-J diphosphate(4-) Chemical compound [O-]P([O-])(=O)OP([O-])([O-])=O XPPKVPWEQAFLFU-UHFFFAOYSA-J 0.000 claims description 4
- 235000011180 diphosphates Nutrition 0.000 claims description 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 4
- 229920000573 polyethylene Polymers 0.000 claims description 4
- 229920001343 polytetrafluoroethylene Polymers 0.000 claims description 4
- LIAWCKFOFPPVGF-UHFFFAOYSA-N 2-ethyladamantane Chemical compound C1C(C2)CC3CC1C(CC)C2C3 LIAWCKFOFPPVGF-UHFFFAOYSA-N 0.000 claims description 2
- YGYAWVDWMABLBF-UHFFFAOYSA-N Phosgene Chemical compound ClC(Cl)=O YGYAWVDWMABLBF-UHFFFAOYSA-N 0.000 claims description 2
- YSMRWXYRXBRSND-UHFFFAOYSA-N TOTP Chemical compound CC1=CC=CC=C1OP(=O)(OC=1C(=CC=CC=1)C)OC1=CC=CC=C1C YSMRWXYRXBRSND-UHFFFAOYSA-N 0.000 claims description 2
- 125000000217 alkyl group Chemical group 0.000 claims description 2
- 150000004650 carbonic acid diesters Chemical class 0.000 claims description 2
- 125000005843 halogen group Chemical group 0.000 claims description 2
- 239000003112 inhibitor Substances 0.000 claims description 2
- 239000000314 lubricant Substances 0.000 claims description 2
- YAFOVCNAQTZDQB-UHFFFAOYSA-N octyl diphenyl phosphate Chemical group C=1C=CC=CC=1OP(=O)(OCCCCCCCC)OC1=CC=CC=C1 YAFOVCNAQTZDQB-UHFFFAOYSA-N 0.000 claims description 2
- 150000002989 phenols Chemical class 0.000 claims description 2
- 239000000049 pigment Substances 0.000 claims description 2
- 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 claims description 2
- KOWVWXQNQNCRRS-UHFFFAOYSA-N tris(2,4-dimethylphenyl) phosphate Chemical compound CC1=CC(C)=CC=C1OP(=O)(OC=1C(=CC(C)=CC=1)C)OC1=CC=C(C)C=C1C KOWVWXQNQNCRRS-UHFFFAOYSA-N 0.000 claims description 2
- 239000012760 heat stabilizer Substances 0.000 claims 1
- 239000011256 inorganic filler Substances 0.000 claims 1
- 229910003475 inorganic filler Inorganic materials 0.000 claims 1
- 239000004611 light stabiliser Substances 0.000 claims 1
- 229920001169 thermoplastic Polymers 0.000 abstract description 5
- 239000004416 thermosoftening plastic Substances 0.000 abstract 1
- 229920000515 polycarbonate Polymers 0.000 description 10
- 239000004417 polycarbonate Substances 0.000 description 10
- XUCNUKMRBVNAPB-UHFFFAOYSA-N fluoroethene Chemical group FC=C XUCNUKMRBVNAPB-UHFFFAOYSA-N 0.000 description 8
- 230000000052 comparative effect Effects 0.000 description 7
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 238000002156 mixing Methods 0.000 description 4
- 230000000704 physical effect Effects 0.000 description 4
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 3
- 230000006866 deterioration Effects 0.000 description 3
- 238000001746 injection moulding Methods 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- 229920005989 resin Polymers 0.000 description 3
- 239000011347 resin Substances 0.000 description 3
- 239000000654 additive Substances 0.000 description 2
- 239000011258 core-shell material Substances 0.000 description 2
- ASMQGLCHMVWBQR-UHFFFAOYSA-M diphenyl phosphate Chemical compound C=1C=CC=CC=1OP(=O)([O-])OC1=CC=CC=C1 ASMQGLCHMVWBQR-UHFFFAOYSA-M 0.000 description 2
- 230000001747 exhibiting effect Effects 0.000 description 2
- 239000000155 melt Substances 0.000 description 2
- 238000000465 moulding Methods 0.000 description 2
- 229940045916 polymetaphosphate Drugs 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- 239000006057 Non-nutritive feed additive Substances 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- 239000003242 anti bacterial agent Substances 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- 239000002216 antistatic agent Substances 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 238000010101 extrusion blow moulding Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 239000011241 protective layer Substances 0.000 description 1
- 238000000197 pyrolysis Methods 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000013589 supplement Substances 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
- C08K5/00—Use of organic ingredients
- C08K5/49—Phosphorus-containing compounds
- C08K5/51—Phosphorus bound to oxygen
- C08K5/52—Phosphorus bound to oxygen only
- C08K5/521—Esters of phosphoric acids, e.g. of H3PO4
- C08K5/523—Esters of phosphoric acids, e.g. of H3PO4 with hydroxyaryl compounds
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L101/00—Compositions of unspecified macromolecular compounds
- C08L101/02—Compositions of unspecified macromolecular compounds characterised by the presence of specified groups, e.g. terminal or pendant functional groups
- C08L101/04—Compositions of unspecified macromolecular compounds characterised by the presence of specified groups, e.g. terminal or pendant functional groups containing halogen atoms
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L27/00—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 a halogen; Compositions of derivatives of such polymers
- C08L27/02—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 a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L27/12—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 a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment containing fluorine atoms
- C08L27/18—Homopolymers or copolymers or tetrafluoroethene
-
- 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
Definitions
- the present invention relates to a non-halogen flame retardant polycarbonate resin composition having excellent infrared transmissivity and non-halogen flame retardancy imparted by incorporating a mixture of aromatic phosphate as a non-halogen flame retardant and fluoroolefin into a polycarbonate resin.
- a polycarbonate resin per se has high infrared transmissivity.
- aromatic phosphate and fluoroolefin which are typically used to impart flame retardancy necessary for an external ornament of electric/electronic products, results in rapid deterioration of infrared transmissivity of the product.
- This approach has low infrared transmissivity, thus suffering from limitations of application thereof to products requiring infrared remote control operation, such as TV front cabinet and the like.
- the present invention has been made in view of the above problems, and it is an object of the present invention to provide a flame retardant polycarbonate resin composition having excellent infrared transmissivity, by using non-halogen aromatic phosphate having excellent compatibility with a polycarbonate resin and thus causing no deterioration of infrared transmissivity even when a given amount of the non-ha logen aromatic phosphate is mixed with the polycarbonate resin and by using fluoroolefin having excellent dispersibility.
- a flame retardant thermoplastic resin composition comprising (A) 83 to 93% by weight of a polycarbonate resin, (B) 6 to 17% by weight of aromatic phosphate, and (C) 0.08 to 0.3% by weight of fluoroolefin.
- the polycarbonate resin is a compound prepared by reacting a divalent phenolic compound with a phosgene or carbonic acid diester and containing no halogen.
- the aromatic phosphate is a non-halogen flame retardant and is selected from aromatic monophosphate, aromatic diphosphate and a mixture thereof.
- the aromatic monophosphate is preferably selected from the group consisting of non-halogen substituted triarylphosphate and trialkyl-arylphosphate.
- the triarylphosphate is selected from the group consisting of triph- enylphosphate, tricresylphosphate, trixylenylphosphate and cresyldiphenylphosphate
- the trialkyl-arylphosphate is preferably octyldiphenylphosphate.
- the aromatic diphosphate is preferably a compound represented by Formula 1:
- Ar to Ar are each independently phenyl or aryl substituted with one to three C -C alkyl, R is phenyl or bisphenol A, and l ⁇ n ⁇ 2.
- the fluoroolefin is preferably selected from fluorinated polyethylene, and fluoroethylene with attachment of a thermoplastic resin or organic material.
- the thermoplastic resin or organic material-bound fluoroethylene may include compounds having a core- shell structure where the core is fluoroethylene and the shell is a thermoplastic resin or organic material, and compounds having fluoroethylene with partial branching of a thermoplastic polymer or organic material.
- the fluoroethylene compound is a compound having partial attachment of a thermoplastic polymer or organic material to fluoroethylene or is a core- shell type compound, superior dispersibility is obtained as compared to use of fluoroethylene alone.
- To fluoroethylene is largely attached a styrene organic material or a thermoplastic polymer partially containing a styrene-based moiety, or an acrylic organic material or a thermoplastic polymer partially containing an acrylic moiety.
- the fluoroethylene is preferably polytetrafluorethylene (PTFE).
- Examples of conventional additives that can be added to the resin composition of the present invention may include an antioxidant, a weathering stabilizer, a lubricant, a silicon supplement, a release agent, a pigment, a dye, an antistatic agent, an antibacterial agent, a processing aid, and antiabrasive. These additives can be used within a proper content.
- mixing of composition components may be carried out by a conventional method involving dry blending of the components, followed by heating and melt-mixing.
- the mixing process is carried out typically at a temperature of 24O 0 C to 300 0 C, preferably 26O 0 C to 27O 0 C, such that the individual components can sufficiently maintain physicochemical affinity therebetween.
- the resulting composition may be subjected to a molding method such as injection molding, extrusion molding, blow molding, or the like, which is conventionally employed in molding of polycarbonate.
- the present invention provides a polycarbonate resin composition with superior infrared transmissivity and flame retardancy. Therefore, the resin composition of the present invention can be used for applications of non-coated external parts of electric/ electronic appliances to which an infrared controller is applied.
- MFI was measured at 300 0 C and a load of 1.2 kg, according to ASTM D 1238.
- PC polycarbonate
- PC polycarbonate
- Comparative Example 2 A specimen was prepared and tested in the same manner as in Comparative Example 1, except that 94.8% by weight of PC, 5% by weight of aromatic phosphate, and 0.3% by weight of fluoroolefin were melt-mixed and pelletized at 28O 0 C to obtain a resin composition. The results are given in Table 1 below.
- Comparative Example 3 A specimen was prepared and tested in the same manner as in Comparative Example 1, except that 87.6% by weight of PC, 12% by weight of aromatic phosphate, and 0.4% by weight of fluoroolefin were used. The results are given in Table 1 below.
- Aromatic phosphate exhibits flame retardancy. That is, when it is combusted, the aromatic phosphate produces polymetaphosphate by pyrolysis and the resulting poly- metaphosphate forms a protective layer on a resin, thereby providing flame retardancy. Fluoroolefin is added to prevent the occurrence of dripping upon combustion of the resin. Higher contents of the aromatic phosphate and fluoroolefin provide higher flame retardancy.
- the content of fluoroolefin exhibits the most significant effects on the infrared transmissivity and flame retardancy.
- the resin composition of the present invention maintain high infrared transmissivity and flame retardancy V-O. It can be seen from Examples 1 to 3 that the resin composition of the present invention exhibiting these effects is a composition containing 6 to 17% by weight of aromatic phosphate and 0.08 to 0.3% by weight of fluoroolefin.
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)
Abstract
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN2008801264512A CN101939381A (zh) | 2007-12-05 | 2008-12-05 | 具有高红外透过性的阻燃的聚碳酸酯树脂组合物 |
US12/866,440 US20110184102A1 (en) | 2007-12-05 | 2008-12-05 | Flame retardant polycarbonate resin composition having high infrared transmission |
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR10-2007-0125402 | 2007-12-05 | ||
KR20070125402 | 2007-12-05 | ||
KR1020080122868A KR101020047B1 (ko) | 2007-12-05 | 2008-12-05 | 난연 열가소성 수지 조성물 |
KR10-2008-0122868 | 2008-12-05 |
Publications (2)
Publication Number | Publication Date |
---|---|
WO2009072846A2 true WO2009072846A2 (fr) | 2009-06-11 |
WO2009072846A3 WO2009072846A3 (fr) | 2009-07-23 |
Family
ID=40718373
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/KR2008/007229 WO2009072846A2 (fr) | 2007-12-05 | 2008-12-05 | Composition de résine de polycarbonate ignifuge dotée d'une transmission infrarouge élevée |
Country Status (1)
Country | Link |
---|---|
WO (1) | WO2009072846A2 (fr) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN105924926A (zh) * | 2016-07-01 | 2016-09-07 | 东莞市海越塑化有限公司 | 一种抗老化可红外穿透的新型复合材料及其制备方法 |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR19980079379A (ko) * | 1997-03-27 | 1998-11-25 | 김윤 | 열변형 온도 특성 및 기계적 특성이 향상된 난연성 고분자 수지조성물 |
KR19990033150A (ko) * | 1997-10-23 | 1999-05-15 | 유현식 | 난연성을 갖는 폴리카보네이트계 열가소성 수지 조성물 |
KR19990033149A (ko) * | 1997-10-23 | 1999-05-15 | 유현식 | 난연성을 갖는 폴리카보네이트계 열가소성 수지 조성물 |
KR100488864B1 (ko) * | 1995-11-01 | 2006-07-06 | 제너럴 일렉트릭 캄파니 | 가열노화안정성을나타내는난연성폴리카보네이트/그라프트블렌드 |
-
2008
- 2008-12-05 WO PCT/KR2008/007229 patent/WO2009072846A2/fr active Application Filing
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR100488864B1 (ko) * | 1995-11-01 | 2006-07-06 | 제너럴 일렉트릭 캄파니 | 가열노화안정성을나타내는난연성폴리카보네이트/그라프트블렌드 |
KR19980079379A (ko) * | 1997-03-27 | 1998-11-25 | 김윤 | 열변형 온도 특성 및 기계적 특성이 향상된 난연성 고분자 수지조성물 |
KR19990033150A (ko) * | 1997-10-23 | 1999-05-15 | 유현식 | 난연성을 갖는 폴리카보네이트계 열가소성 수지 조성물 |
KR19990033149A (ko) * | 1997-10-23 | 1999-05-15 | 유현식 | 난연성을 갖는 폴리카보네이트계 열가소성 수지 조성물 |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN105924926A (zh) * | 2016-07-01 | 2016-09-07 | 东莞市海越塑化有限公司 | 一种抗老化可红外穿透的新型复合材料及其制备方法 |
Also Published As
Publication number | Publication date |
---|---|
WO2009072846A3 (fr) | 2009-07-23 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
TWI492987B (zh) | 非鹵素阻燃劑及高硬度聚碳酸酯樹脂組成物 | |
JP4990965B2 (ja) | 耐スクラッチ性−難燃性の熱可塑性樹脂組成物 | |
US7671143B2 (en) | Flame retardant polycarbonate resin composition having good impact, high heat resistance | |
TWI394798B (zh) | 具有優異阻燃性之聚碳酸酯樹脂組成物 | |
KR101411009B1 (ko) | 폴리카보네이트 수지 조성물 및 이를 포함하는 성형품 | |
KR101411004B1 (ko) | 아크릴계 공중합체 수지 조성물 | |
US20110184102A1 (en) | Flame retardant polycarbonate resin composition having high infrared transmission | |
KR101262306B1 (ko) | 난연성 폴리카보네이트 수지 조성물 | |
KR20000009218A (ko) | 열가소성 수지 조성물 | |
US11091604B2 (en) | Thermoplastic resin composition having excellent electrical properties, and molded article produced using same | |
KR20000041993A (ko) | 내충격성이 우수한 난연성을 갖는 폴리카보네이트계 열가소성수지 조성물 | |
WO2009072846A2 (fr) | Composition de résine de polycarbonate ignifuge dotée d'une transmission infrarouge élevée | |
KR101262309B1 (ko) | 난연성 폴리카보네이트 수지 조성물 | |
TWI404763B (zh) | 抗刮聚碳酸酯樹脂組成物及成形物件 | |
KR101820245B1 (ko) | 난연 및 유동성이 개선된 폴리카보네이트 수지 조성물 | |
KR101435084B1 (ko) | 폴리카보네이트 수지 조성물 | |
CN114231003B (zh) | 一种透明阻燃聚碳酸酯复合材料及其制备方法和应用 | |
KR101743330B1 (ko) | 난연성 열가소성 수지 조성물 및 이를 포함하는 성형품 | |
KR101374429B1 (ko) | 투명성 및 난연성이 우수한 폴리카보네이트 수지 조성물 및 이를 이용한 제품 | |
KR100211180B1 (ko) | 난연성을 갖는 열가소성 폴리카보네이트계 수지 조성물 | |
KR100340214B1 (ko) | 난연성이 우수한 열가소성 수지 조성물 | |
KR102060559B1 (ko) | 가공성이 우수한 난연 폴리카보네이트 수지 조성물 및 이를 이용한 성형품 | |
KR20190063833A (ko) | 난연성 및 열안정성이 우수한 유리섬유 강화 폴리카보네이트 수지 조성물 | |
CN102134382A (zh) | 无卤阻燃的高硬度聚碳酸酯合金的配方 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
WWE | Wipo information: entry into national phase |
Ref document number: 200880126451.2 Country of ref document: CN |
|
121 | Ep: the epo has been informed by wipo that ep was designated in this application |
Ref document number: 08858270 Country of ref document: EP Kind code of ref document: A2 |
|
NENP | Non-entry into the national phase in: |
Ref country code: DE |
|
122 | Ep: pct application non-entry in european phase |
Ref document number: 08858270 Country of ref document: EP Kind code of ref document: A2 |
|
WWE | Wipo information: entry into national phase |
Ref document number: 12866440 Country of ref document: US |