CA1199745A - Compose d'ether de polyphenylene, de resine de styrene et de phosphonate cyclique pour articles moules ignifuges - Google Patents

Compose d'ether de polyphenylene, de resine de styrene et de phosphonate cyclique pour articles moules ignifuges

Info

Publication number: CA1199745A
Authority: CA; Canada
Prior art keywords: composition; parts; component; carbon atoms; weight
Prior art date: 1977-09-06
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

CA000309985A

Other languages

English (en)

Inventor

Robert J. Axelrod

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.)

1977-09-06

Filing date

1978-08-24

Publication date

1986-01-21

1978-08-24 Application filed by General Electric Co filed Critical General Electric Co

1986-01-21 Application granted granted Critical

1986-01-21 Publication of CA1199745A publication Critical patent/CA1199745A/fr

Status Expired legal-status Critical Current

Links

239000000203 mixture Substances 0.000 title claims abstract description 65
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 title claims abstract description 55
229920005989 resin Polymers 0.000 title claims abstract description 44
239000011347 resin Substances 0.000 title claims abstract description 44
239000003063 flame retardant Substances 0.000 title claims abstract description 21
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 abstract description 16
UEZVMMHDMIWARA-UHFFFAOYSA-M phosphonate Chemical compound [O-]P(=O)=O UEZVMMHDMIWARA-UHFFFAOYSA-M 0.000 title claims abstract description 12
229920001955 polyphenylene ether Polymers 0.000 title claims description 15
125000004122 cyclic group Chemical group 0.000 title abstract description 9
-1 poly-phenylene ether Chemical compound 0.000 claims abstract description 21
238000000465 moulding Methods 0.000 claims abstract description 4
125000004432 carbon atom Chemical group C* 0.000 claims description 30
125000000217 alkyl group Chemical group 0.000 claims description 16
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 14
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 12
125000004435 hydrogen atom Chemical class [H]* 0.000 claims description 11
229910052736 halogen Inorganic materials 0.000 claims description 9
150000002367 halogens Chemical class 0.000 claims description 9
229910052739 hydrogen Inorganic materials 0.000 claims description 9
239000001257 hydrogen Substances 0.000 claims description 9
229910052799 carbon Inorganic materials 0.000 claims description 8
150000001875 compounds Chemical class 0.000 claims description 7
125000003118 aryl group Chemical group 0.000 claims description 6
150000001555 benzenes Chemical class 0.000 claims description 6
125000002877 alkyl aryl group Chemical group 0.000 claims description 5
125000005843 halogen group Chemical group 0.000 claims description 5
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 4
125000002704 decyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 4
229920001169 thermoplastic Polymers 0.000 claims description 4
239000004416 thermosoftening plastic Substances 0.000 claims description 4
239000004215 Carbon black (E152) Substances 0.000 claims description 3
229920001971 elastomer Polymers 0.000 claims description 3
229920005669 high impact polystyrene Polymers 0.000 claims description 3
229930195733 hydrocarbon Natural products 0.000 claims description 3
229910052760 oxygen Inorganic materials 0.000 claims description 3
239000001301 oxygen Substances 0.000 claims description 3
239000005060 rubber Substances 0.000 claims description 3
125000001424 substituent group Chemical group 0.000 claims description 3
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 3
229920002554 vinyl polymer Polymers 0.000 claims description 3
239000004797 high-impact polystyrene Substances 0.000 claims 2
125000003710 aryl alkyl group Chemical group 0.000 claims 1
230000000979 retarding effect Effects 0.000 claims 1
230000000704 physical effect Effects 0.000 abstract description 3
GMEVZRPQNQEJHG-UHFFFAOYSA-N 2,2-bis(hydroxymethyl)-1,1-diphenylpropane-1,3-diol Chemical compound C1(=CC=CC=C1)C(O)(C(CO)(CO)CO)C1=CC=CC=C1 GMEVZRPQNQEJHG-UHFFFAOYSA-N 0.000 abstract 1
RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 abstract 1
239000004793 Polystyrene Substances 0.000 description 5
229920002223 polystyrene Polymers 0.000 description 5
238000002485 combustion reaction Methods 0.000 description 4
229920001577 copolymer Polymers 0.000 description 4
238000000034 method Methods 0.000 description 4
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 4
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
239000000463 material Substances 0.000 description 3
MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 description 2
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
229920000147 Styrene maleic anhydride Polymers 0.000 description 2
239000000654 additive Substances 0.000 description 2
125000004429 atom Chemical group 0.000 description 2
238000001125 extrusion Methods 0.000 description 2
239000008187 granular material Substances 0.000 description 2
150000002500 ions Chemical class 0.000 description 2
229920001897 terpolymer Polymers 0.000 description 2
125000001140 1,4-phenylene group Chemical group [H]C1=C([H])C([*:2])=C([H])C([H])=C1[*:1] 0.000 description 1
125000000094 2-phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 description 1
PYSRRFNXTXNWCD-UHFFFAOYSA-N 3-(2-phenylethenyl)furan-2,5-dione Chemical compound O=C1OC(=O)C(C=CC=2C=CC=CC=2)=C1 PYSRRFNXTXNWCD-UHFFFAOYSA-N 0.000 description 1
JDCCCHBBXRQRGU-UHFFFAOYSA-N 5-phenylpenta-2,4-dienenitrile Chemical compound N#CC=CC=CC1=CC=CC=C1 JDCCCHBBXRQRGU-UHFFFAOYSA-N 0.000 description 1
229920000742 Cotton Polymers 0.000 description 1
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
AFCARXCZXQIEQB-UHFFFAOYSA-N N-[3-oxo-3-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)propyl]-2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidine-5-carboxamide Chemical compound O=C(CCNC(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F)N1CC2=C(CC1)NN=N2 AFCARXCZXQIEQB-UHFFFAOYSA-N 0.000 description 1
RLXOKISGPALBEB-UHFFFAOYSA-N OP(=O)OP(O)=O.OCC(CO)(CO)CO Chemical class OP(=O)OP(O)=O.OCC(CO)(CO)CO RLXOKISGPALBEB-UHFFFAOYSA-N 0.000 description 1
229910019142 PO4 Inorganic materials 0.000 description 1
239000002250 absorbent Substances 0.000 description 1
230000002745 absorbent Effects 0.000 description 1
XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 description 1
MPMBRWOOISTHJV-UHFFFAOYSA-N but-1-enylbenzene Chemical compound CCC=CC1=CC=CC=C1 MPMBRWOOISTHJV-UHFFFAOYSA-N 0.000 description 1
125000005587 carbonate group Chemical group 0.000 description 1
238000006243 chemical reaction Methods 0.000 description 1
230000001419 dependent effect Effects 0.000 description 1
IBDMRHDXAQZJAP-UHFFFAOYSA-N dichlorophosphorylbenzene Chemical compound ClP(Cl)(=O)C1=CC=CC=C1 IBDMRHDXAQZJAP-UHFFFAOYSA-N 0.000 description 1
150000002170 ethers Chemical class 0.000 description 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
BCDGQXUMWHRQCB-UHFFFAOYSA-N glycine methyl ketone Natural products CC(=O)CN BCDGQXUMWHRQCB-UHFFFAOYSA-N 0.000 description 1
229920001519 homopolymer Polymers 0.000 description 1
BHEPBYXIRTUNPN-UHFFFAOYSA-N hydridophosphorus(.) (triplet) Chemical compound [PH] BHEPBYXIRTUNPN-UHFFFAOYSA-N 0.000 description 1
238000002347 injection Methods 0.000 description 1
239000007924 injection Substances 0.000 description 1
238000001746 injection moulding Methods 0.000 description 1
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
239000000314 lubricant Substances 0.000 description 1
125000001624 naphthyl group Chemical group 0.000 description 1
125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
239000002245 particle Substances 0.000 description 1
239000008188 pellet Substances 0.000 description 1
WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
235000021317 phosphate Nutrition 0.000 description 1
239000000049 pigment Substances 0.000 description 1
239000004014 plasticizer Substances 0.000 description 1
229920000642 polymer Polymers 0.000 description 1
229920005990 polystyrene resin Polymers 0.000 description 1
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
PWZUUYSISTUNDW-VAFBSOEGSA-N quinestrol Chemical compound C([C@@H]1[C@@H](C2=CC=3)CC[C@]4([C@H]1CC[C@@]4(O)C#C)C)CC2=CC=3OC1CCCC1 PWZUUYSISTUNDW-VAFBSOEGSA-N 0.000 description 1
238000001953 recrystallisation Methods 0.000 description 1
230000002787 reinforcement Effects 0.000 description 1
239000003381 stabilizer Substances 0.000 description 1
125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
229920003048 styrene butadiene rubber Polymers 0.000 description 1
239000000126 substance Substances 0.000 description 1
239000000725 suspension Substances 0.000 description 1
229920003002 synthetic resin Polymers 0.000 description 1
239000000057 synthetic resin Substances 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
- C08K5/49—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
- C08K5/5357—Esters of phosphonic acids cyclic
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/6564—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms
- C07F9/6571—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms having phosphorus and oxygen atoms as the only ring hetero atoms
- C07F9/657163—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms having phosphorus and oxygen atoms as the only ring hetero atoms the ring phosphorus atom being bound to at least one carbon atom
- C07F9/657181—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms having phosphorus and oxygen atoms as the only ring hetero atoms the ring phosphorus atom being bound to at least one carbon atom the ring phosphorus atom and, at least, one ring oxygen atom being part of a (thio)phosphonic acid derivative
- 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
- 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
- C08L25/04—Homopolymers or copolymers of styrene
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L71/00—Compositions of polyethers obtained by reactions forming an ether link in the main chain; Compositions of derivatives of such polymers
- C08L71/02—Polyalkylene oxides
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2201/00—Properties
- C08L2201/02—Flame or fire retardant/resistant
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L71/00—Compositions of polyethers obtained by reactions forming an ether link in the main chain; Compositions of derivatives of such polymers
- C08L71/08—Polyethers derived from hydroxy compounds or from their metallic derivatives
- C08L71/10—Polyethers derived from hydroxy compounds or from their metallic derivatives from phenols
- C08L71/12—Polyphenylene oxides

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Health & Medical Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Life Sciences & Earth Sciences (AREA)
Biochemistry (AREA)
General Health & Medical Sciences (AREA)
Molecular Biology (AREA)
Compositions Of Macromolecular Compounds (AREA)
Fireproofing Substances (AREA)

CA000309985A 1977-09-06 1978-08-24 Compose d'ether de polyphenylene, de resine de styrene et de phosphonate cyclique pour articles moules ignifuges Expired CA1199745A (fr)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
US83105677A	1977-09-06	1977-09-06
US831,056		1977-09-06

Publications (1)

Publication Number	Publication Date
CA1199745A true CA1199745A (fr)	1986-01-21

Family

ID=25258195

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CA000309985A Expired CA1199745A (fr)	1977-09-06	1978-08-24	Compose d'ether de polyphenylene, de resine de styrene et de phosphonate cyclique pour articles moules ignifuges

Country Status (7)

Country	Link
JP (1)	JPS5460354A (fr)
AU (1)	AU3955078A (fr)
CA (1)	CA1199745A (fr)
DE (1)	DE2836771A1 (fr)
FR (1)	FR2401956A1 (fr)
GB (1)	GB2003888B (fr)
NL (1)	NL7809098A (fr)

Families Citing this family (14)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4402882A (en) *	1980-09-02	1983-09-06	Ciba-Geigy Corporation	Process for the production of diphosphaspiro compounds
DE3105946A1 (de)	1981-02-18	1982-08-19	Basf Ag, 6700 Ludwigshafen	Selbstverloeschende thermoplastische formmassen
EP0075863A1 (fr) *	1981-09-25	1983-04-06	General Electric Company	Composition de résine de polyéther de phénylène et d'une résine alcényle aromatique
US6797754B2 (en)	2002-05-06	2004-09-28	Cheil Industries Inc.	Flame retardant styrenic compositions containing oxaphospholane compound as flame retardant
US7087667B2 (en)	2001-05-15	2006-08-08	Teijin Chemicals, Ltd.	Flame-retardant resin composition and molded article therefrom
WO2004029143A1 (fr) *	2002-09-25	2004-04-08	Cheil Industries Inc.	Composition de resine styrene ignifuge
AU2003304381A1 (en)	2003-08-04	2005-02-15	Cheil Industries Inc.	Flameproof thermoplastic resin composition
KR100505317B1 (ko)	2003-08-04	2005-08-02	제일모직주식회사	난연성 열가소성 수지 조성물
CN1820047B (zh)	2003-08-14	2010-10-13	第一毛织株式会社	防火橡胶-强化苯乙烯树脂组合物
KR100506067B1 (ko)	2003-08-14	2005-08-03	제일모직주식회사	난연성 열가소성 수지 조성물
CN101228231B (zh)	2005-08-08	2012-06-06	第一毛织株式会社	阻燃性模塑组合物
KR100817399B1 (ko)	2005-12-29	2008-03-27	제일모직주식회사	난연성 열가소성 수지 조성물
US20090163627A1 (en)	2007-12-20	2009-06-25	Cheil Industries Inc.	Symmetric Cyclic Phosphonate Compound, Method of Preparing the Same and Flame Retardant Styrenic Resin Composition Including the Same
JP5502819B2 (ja) *	2011-08-24	2014-05-28	帝人株式会社	難燃性樹脂組成物およびそれからの成形品

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3141031A (en) *	1960-08-23	1964-07-14	Ethyl Corp	Olefin cobalt carbonyl compounds
US3997505A (en) *	1974-01-02	1976-12-14	Michigan Chemical Corporation	Flame retardant polymeric compositions containing pentaerythritol cyclic diphosphates or diphosphoramidates
CH596332A5 (fr) *	1975-07-15	1978-03-15	Ciba Geigy Ag

1978
- 1978-08-21 GB GB7833991A patent/GB2003888B/en not_active Expired
- 1978-08-23 DE DE19782836771 patent/DE2836771A1/de not_active Withdrawn
- 1978-08-24 CA CA000309985A patent/CA1199745A/fr not_active Expired
- 1978-09-05 JP JP10818578A patent/JPS5460354A/ja active Pending
- 1978-09-05 AU AU39550/78A patent/AU3955078A/en active Pending
- 1978-09-05 FR FR7825476A patent/FR2401956A1/fr not_active Withdrawn
- 1978-09-06 NL NL7809098A patent/NL7809098A/xx not_active Application Discontinuation

Also Published As

Publication number	Publication date
GB2003888A (en)	1979-03-21
GB2003888B (en)	1982-02-03
FR2401956A1 (fr)	1979-03-30
AU3955078A (en)	1980-03-13
JPS5460354A (en)	1979-05-15
DE2836771A1 (de)	1979-03-15
NL7809098A (nl)	1979-03-08

Legal Events

Date	Code	Title	Description
2003-01-21	MKEX	Expiry

Publication	Publication Date	Title
CA1109182A (fr)	1981-09-15	Produit retardateur de flammes a base d'ether de polyphenylene, d'une resine de styrene et d'un phosphate cyclique
US4526917A (en)	1985-07-02	Flame retardant mixture of triaryl phosphates and resinous compositions thereof
US3883613A (en)	1975-05-13	Flame retardant composition of polyphenylene ether, styrene resin and trimesityl phosphate and process for the preparation thereof
US6166115A (en)	2000-12-26	Flame resistant polyphenylene ether-polyamide resin blends
NL7901769A (nl)	1980-09-09	Vlamvertragende, polyfenyleenether bevattende samen- stellingen.
EP1651718B1 (fr)	2009-03-11	Composition de resine thermoplastique ignifuge
US5973041A (en)	1999-10-26	Resinous compositions containing aromatic bisphosphoramidates as flame retardants
US4405739A (en)	1983-09-20	Polyphenylene ether resins and compositions heat stabilized with phosphite compounds
US4520152A (en)	1985-05-28	Flame retardant composition of polyphenylene ether, styrene resin and cyclic phosphonate
US6124385A (en)	2000-09-26	Halogen-free flame resistant polystyrol moulding materials
EP1654321B1 (fr)	2012-10-10	Composition de resine styrenique ignifuge renforcee par du caoutchouc
JP2003529654A (ja)	2003-10-07	透明な難燃性ポリ（アリーレンエーテル）ブレンド
US4123474A (en)	1978-10-31	Polyphenylene ether resin compositions containing a diphenylamine
KR100598452B1 (ko)	2006-07-10	난연성 스티렌계 수지조성물
US4390477A (en)	1983-06-28	Diphenyl pentaerythritol diphosphonate
DE60036823T2 (de)	2008-06-19	Flammhemmende harzzusammensetzung und daraus hergestellter formkörper
CA1101579A (fr)	1981-05-19	Traduction non-disponible
EP0176774B1 (fr)	1991-12-27	Masse à mouler thermoplastique auto-extinguible exempte d'halogène
GB2078226A (en)	1982-01-06	Flame retardant mixture and resinous compositions including the mixture
JPS61200163A (ja)	1986-09-04	難燃性に優れたポリフエニレンエ−テル系樹脂組成物
CA1198541A (fr)	1985-12-24	Compositions de resine thrmoplastique ignifuge a base de poly(oxyde de phenylene-styrene)
EP0207380B1 (fr)	1990-09-12	Matières thermoplastiques à base d'oxyde de polyphénylène retardateur de flamme
US4584332A (en)	1986-04-22	Flame retardant polyphenylene oxide thermoplastics
US6479572B1 (en)	2002-11-12	Thermoplastic molding materials stable to thermal oxidation
EP0244393B1 (fr)	1993-06-23	Matières à mouler à base de polyphénylène éthers retardateurs de flamme