JPS5855983B2 - 耐燃性ポリカ−ボネ−ト組成物 - Google Patents

耐燃性ポリカ−ボネ−ト組成物

Info

Publication number: JPS5855983B2
Authority: JP; Japan
Prior art keywords: flame; mixture; carbonate; dihydric phenol; weight
Prior art date: 1973-10-01
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

Application number

JP11238074A

Other languages

English (en)

Japanese (ja)

Other versions

JPS5077457A (fr

Inventor

ベンジヤミンル−スジヨン

アルトンボ−ンジユニアハワ−ド

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

General Electric Co

Original Assignee

General Electric Co

Priority date (The priority date 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 date listed.)

1973-10-01

Filing date

1974-10-01

Publication date

1983-12-13

1974-10-01 Application filed by General Electric Co filed Critical General Electric Co

1975-06-24 Publication of JPS5077457A publication Critical patent/JPS5077457A/ja

1983-12-13 Publication of JPS5855983B2 publication Critical patent/JPS5855983B2/ja

Status Expired legal-status Critical Current

Links

239000000203 mixture Substances 0.000 title claims description 50
239000004417 polycarbonate Substances 0.000 title claims description 21
229920000515 polycarbonate Polymers 0.000 title claims description 21
BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 claims description 27
125000003118 aryl group Chemical group 0.000 claims description 26
229920000642 polymer Polymers 0.000 claims description 26
ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 23
229920005645 diorganopolysiloxane polymer Polymers 0.000 claims description 8
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 5
125000000217 alkyl group Chemical group 0.000 claims description 4
125000001424 substituent group Chemical group 0.000 claims 1
IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical class C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 24
-1 tetrachlorophenyl groups Chemical group 0.000 description 17
239000000463 material Substances 0.000 description 14
239000000654 additive Substances 0.000 description 12
229940106691 bisphenol a Drugs 0.000 description 12
ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 10
230000000996 additive effect Effects 0.000 description 10
238000007706 flame test Methods 0.000 description 10
229920001296 polysiloxane Polymers 0.000 description 8
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 6
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 6
229910052794 bromium Inorganic materials 0.000 description 6
238000000034 method Methods 0.000 description 6
239000002245 particle Substances 0.000 description 6
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 6
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 5
239000000370 acceptor Substances 0.000 description 5
239000012530 fluid Substances 0.000 description 5
229920001519 homopolymer Polymers 0.000 description 5
125000000962 organic group Chemical group 0.000 description 5
239000001294 propane Substances 0.000 description 5
GJYCVCVHRSWLNY-UHFFFAOYSA-N 2-butylphenol Chemical compound CCCCC1=CC=CC=C1O GJYCVCVHRSWLNY-UHFFFAOYSA-N 0.000 description 4
VEORPZCZECFIRK-UHFFFAOYSA-N 3,3',5,5'-tetrabromobisphenol A Chemical compound C=1C(Br)=C(O)C(Br)=CC=1C(C)(C)C1=CC(Br)=C(O)C(Br)=C1 VEORPZCZECFIRK-UHFFFAOYSA-N 0.000 description 4
QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 4
239000004594 Masterbatch (MB) Substances 0.000 description 4
229920001577 copolymer Polymers 0.000 description 4
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 4
150000002989 phenols Chemical class 0.000 description 4
229920000742 Cotton Polymers 0.000 description 3
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
KYPYTERUKNKOLP-UHFFFAOYSA-N Tetrachlorobisphenol A Chemical compound C=1C(Cl)=C(O)C(Cl)=CC=1C(C)(C)C1=CC(Cl)=C(O)C(Cl)=C1 KYPYTERUKNKOLP-UHFFFAOYSA-N 0.000 description 3
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
229910052736 halogen Inorganic materials 0.000 description 3
150000002367 halogens Chemical class 0.000 description 3
239000008188 pellet Substances 0.000 description 3
239000002243 precursor Substances 0.000 description 3
150000003462 sulfoxides Chemical class 0.000 description 3
238000010998 test method Methods 0.000 description 3
RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 2
229930185605 Bisphenol Natural products 0.000 description 2
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
YGYAWVDWMABLBF-UHFFFAOYSA-N Phosgene Chemical compound ClC(Cl)=O YGYAWVDWMABLBF-UHFFFAOYSA-N 0.000 description 2
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
239000002253 acid Substances 0.000 description 2
150000004649 carbonic acid derivatives Chemical class 0.000 description 2
SZPIKCAXBLKNNK-UHFFFAOYSA-N dimethyl-phenoxy-phenylsilane Chemical class C=1C=CC=CC=1[Si](C)(C)OC1=CC=CC=C1 SZPIKCAXBLKNNK-UHFFFAOYSA-N 0.000 description 2
VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
150000007522 mineralic acids Chemical class 0.000 description 2
239000003607 modifier Substances 0.000 description 2
150000007524 organic acids Chemical class 0.000 description 2
239000000843 powder Substances 0.000 description 2
GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 2
150000003457 sulfones Chemical class 0.000 description 2
IYMHDNMZTMQXJC-UHFFFAOYSA-N (2,4-dichloro-3-phenylnaphthalen-1-yl) hydrogen carbonate Chemical compound ClC=1C2=CC=CC=C2C(OC(=O)O)=C(Cl)C=1C1=CC=CC=C1 IYMHDNMZTMQXJC-UHFFFAOYSA-N 0.000 description 1
ZGSHFDSKHTZINF-UHFFFAOYSA-N (2-methyl-6-phenylphenyl) hydrogen carbonate Chemical compound CC1=CC=CC(C=2C=CC=CC=2)=C1OC(O)=O ZGSHFDSKHTZINF-UHFFFAOYSA-N 0.000 description 1
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 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
BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical compound OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 description 1
VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
JLTDJTHDQAWBAV-UHFFFAOYSA-N N,N-dimethylaniline Chemical compound CN(C)C1=CC=CC=C1 JLTDJTHDQAWBAV-UHFFFAOYSA-N 0.000 description 1
229910019142 PO4 Inorganic materials 0.000 description 1
239000002202 Polyethylene glycol Substances 0.000 description 1
XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical group [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
229910000272 alkali metal oxide Inorganic materials 0.000 description 1
150000001340 alkali metals Chemical class 0.000 description 1
229910001860 alkaline earth metal hydroxide Inorganic materials 0.000 description 1
125000005037 alkyl phenyl group Chemical group 0.000 description 1
239000002216 antistatic agent Substances 0.000 description 1
DSEORJACOQDMQX-UHFFFAOYSA-N bis(2,3,4-trichlorophenyl) carbonate Chemical compound ClC1=C(Cl)C(Cl)=CC=C1OC(=O)OC1=CC=C(Cl)C(Cl)=C1Cl DSEORJACOQDMQX-UHFFFAOYSA-N 0.000 description 1
LUQQDEDMRRRWGN-UHFFFAOYSA-N bis(2-bromophenyl) carbonate Chemical compound BrC1=CC=CC=C1OC(=O)OC1=CC=CC=C1Br LUQQDEDMRRRWGN-UHFFFAOYSA-N 0.000 description 1
SJWFGMZZMOUDTF-UHFFFAOYSA-N bis(2-chloronaphthalen-1-yl) carbonate Chemical compound C1=CC=C2C(OC(=O)OC3=C4C=CC=CC4=CC=C3Cl)=C(Cl)C=CC2=C1 SJWFGMZZMOUDTF-UHFFFAOYSA-N 0.000 description 1
MUCRFDZUHPMASM-UHFFFAOYSA-N bis(2-chlorophenyl) carbonate Chemical compound ClC1=CC=CC=C1OC(=O)OC1=CC=CC=C1Cl MUCRFDZUHPMASM-UHFFFAOYSA-N 0.000 description 1
POZGCGJFBOZPCM-UHFFFAOYSA-N bis(2-methylphenyl) carbonate Chemical compound CC1=CC=CC=C1OC(=O)OC1=CC=CC=C1C POZGCGJFBOZPCM-UHFFFAOYSA-N 0.000 description 1
MOIPGXQKZSZOQX-UHFFFAOYSA-N carbonyl bromide Chemical compound BrC(Br)=O MOIPGXQKZSZOQX-UHFFFAOYSA-N 0.000 description 1
238000006243 chemical reaction Methods 0.000 description 1
229910052801 chlorine Inorganic materials 0.000 description 1
239000000460 chlorine Substances 0.000 description 1
238000002485 combustion reaction Methods 0.000 description 1
238000013329 compounding Methods 0.000 description 1
238000007334 copolymerization reaction Methods 0.000 description 1
HPXRVTGHNJAIIH-UHFFFAOYSA-N cyclohexanol Chemical compound OC1CCCCC1 HPXRVTGHNJAIIH-UHFFFAOYSA-N 0.000 description 1
229940117389 dichlorobenzene Drugs 0.000 description 1
125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 1
ZQUZPFYNEARCQO-UHFFFAOYSA-N dinaphthalen-1-yl carbonate Chemical compound C1=CC=C2C(OC(OC=3C4=CC=CC=C4C=CC=3)=O)=CC=CC2=C1 ZQUZPFYNEARCQO-UHFFFAOYSA-N 0.000 description 1
230000000694 effects Effects 0.000 description 1
239000003063 flame retardant Substances 0.000 description 1
150000002334 glycols Chemical class 0.000 description 1
125000005059 halophenyl group Chemical group 0.000 description 1
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
238000002347 injection Methods 0.000 description 1
239000007924 injection Substances 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
239000006082 mold release agent Substances 0.000 description 1
238000000465 moulding Methods 0.000 description 1
125000005375 organosiloxane group Chemical group 0.000 description 1
125000004430 oxygen atom Chemical group O* 0.000 description 1
230000000737 periodic effect Effects 0.000 description 1
150000008379 phenol ethers Chemical class 0.000 description 1
NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
239000010452 phosphate Substances 0.000 description 1
239000000049 pigment Substances 0.000 description 1
229920001223 polyethylene glycol Polymers 0.000 description 1
239000011148 porous material Substances 0.000 description 1
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
239000012260 resinous material Substances 0.000 description 1
239000003381 stabilizer Substances 0.000 description 1
150000003512 tertiary amines Chemical class 0.000 description 1
229920001169 thermoplastic Polymers 0.000 description 1
239000004416 thermosoftening plastic Substances 0.000 description 1
IMFACGCPASFAPR-UHFFFAOYSA-N tributylamine Chemical compound CCCCN(CCCC)CCCC IMFACGCPASFAPR-UHFFFAOYSA-N 0.000 description 1
125000004360 trifluorophenyl group Chemical group 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

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)

JP11238074A 1973-10-01 1974-10-01 耐燃性ポリカ−ボネ−ト組成物 Expired JPS5855983B2 (ja)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
US40197273A	1973-10-01	1973-10-01
US401972		1973-10-01

Publications (2)

Publication Number	Publication Date
JPS5077457A JPS5077457A (fr)	1975-06-24
JPS5855983B2 true JPS5855983B2 (ja)	1983-12-13

Family

ID=23590021

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP11238074A Expired JPS5855983B2 (ja)	1973-10-01	1974-10-01	耐燃性ポリカ−ボネ−ト組成物

Country Status (8)

Country	Link
JP (1)	JPS5855983B2 (fr)
BR (1)	BR7408042D0 (fr)
CA (1)	CA1059681A (fr)
DE (1)	DE2446423A1 (fr)
FR (1)	FR2246602A1 (fr)
GB (1)	GB1483084A (fr)
IT (1)	IT1022445B (fr)
NL (1)	NL7412846A (fr)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
GB1519561A (en) *	1976-08-26	1978-08-02	Gen Tire & Rubber Co	Polycarbonate composition
JPS5674124A (en) *	1979-11-20	1981-06-19	Mitsubishi Chem Ind Ltd	Preparation of polycarbonate resin containing halogen
JPS60184551A (ja) *	1984-03-02	1985-09-20	Teijin Chem Ltd	難燃性ポリカ−ボネ−ト樹脂組成物
DE3640582A1 (de) *	1986-11-27	1988-06-09	Bayer Ag	Silikonkautschuk enthaltende polymerisatpulver, ihre herstellung und anwendung als flammhemmendes additiv
US4923933A (en) *	1989-01-06	1990-05-08	General Electric Company	Polycarbonate/polyphthalate carbonate blends exhibiting good flame resistance
CN100506914C (zh) *	2007-04-09	2009-07-01	杭州师范学院	抑烟型无卤阻燃聚碳酸酯

1974
- 1974-08-27 CA CA207,833A patent/CA1059681A/fr not_active Expired
- 1974-09-11 GB GB3964074A patent/GB1483084A/en not_active Expired
- 1974-09-27 BR BR804274A patent/BR7408042D0/pt unknown
- 1974-09-27 NL NL7412846A patent/NL7412846A/xx not_active Application Discontinuation
- 1974-09-28 DE DE19742446423 patent/DE2446423A1/de not_active Withdrawn
- 1974-09-30 IT IT2787574A patent/IT1022445B/it active
- 1974-10-01 JP JP11238074A patent/JPS5855983B2/ja not_active Expired
- 1974-10-01 FR FR7432986A patent/FR2246602A1/fr not_active Withdrawn

Also Published As

Publication number	Publication date
IT1022445B (it)	1978-03-20
BR7408042D0 (pt)	1975-09-16
NL7412846A (nl)	1975-04-03
FR2246602A1 (fr)	1975-05-02
AU7378474A (en)	1976-04-01
JPS5077457A (fr)	1975-06-24
CA1059681A (fr)	1979-07-31
GB1483084A (en)	1977-08-17
DE2446423A1 (de)	1975-04-03

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