TW201030013A - Phosphorus-containing silsesquioxane derivatives as flame retardants - Google Patents
Phosphorus-containing silsesquioxane derivatives as flame retardants Download PDFInfo
- Publication number
- TW201030013A TW201030013A TW098137247A TW98137247A TW201030013A TW 201030013 A TW201030013 A TW 201030013A TW 098137247 A TW098137247 A TW 098137247A TW 98137247 A TW98137247 A TW 98137247A TW 201030013 A TW201030013 A TW 201030013A
- Authority
- TW
- Taiwan
- Prior art keywords
- phosphorus
- group
- less
- sesquiterpene oxide
- thermosetting resin
- Prior art date
Links
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 title claims abstract description 22
- 229910052698 phosphorus Inorganic materials 0.000 title claims abstract description 22
- 239000011574 phosphorus Substances 0.000 title claims abstract description 22
- 239000003063 flame retardant Substances 0.000 title description 14
- 239000000203 mixture Substances 0.000 claims abstract description 24
- 125000001183 hydrocarbyl group Chemical group 0.000 claims abstract description 9
- 229920001187 thermosetting polymer Polymers 0.000 claims description 24
- 229920005989 resin Polymers 0.000 claims description 23
- 239000011347 resin Substances 0.000 claims description 23
- 229930004725 sesquiterpene Natural products 0.000 claims description 23
- 150000004354 sesquiterpene derivatives Chemical class 0.000 claims description 21
- 229920000647 polyepoxide Polymers 0.000 claims description 15
- 239000003822 epoxy resin Substances 0.000 claims description 14
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 10
- 239000003795 chemical substances by application Substances 0.000 claims description 7
- 239000000126 substance Substances 0.000 claims description 7
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims description 6
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 5
- 125000000217 alkyl group Chemical group 0.000 claims description 4
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims description 4
- 125000004432 carbon atom Chemical group C* 0.000 claims description 3
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 3
- 125000003983 fluorenyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3CC12)* 0.000 claims 1
- 238000012360 testing method Methods 0.000 description 14
- 230000000052 comparative effect Effects 0.000 description 10
- -1 linear Chemical group 0.000 description 10
- 125000003118 aryl group Chemical group 0.000 description 6
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 6
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 6
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 6
- YTPFRRRNIYVFFE-UHFFFAOYSA-N 2,2,3,3,5,5-hexamethyl-1,4-dioxane Chemical compound CC1(C)COC(C)(C)C(C)(C)O1 YTPFRRRNIYVFFE-UHFFFAOYSA-N 0.000 description 5
- 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 5
- 239000006227 byproduct Substances 0.000 description 5
- 239000000047 product Substances 0.000 description 5
- 238000010438 heat treatment Methods 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- KUBDPQJOLOUJRM-UHFFFAOYSA-N 2-(chloromethyl)oxirane;4-[2-(4-hydroxyphenyl)propan-2-yl]phenol Chemical compound ClCC1CO1.C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 KUBDPQJOLOUJRM-UHFFFAOYSA-N 0.000 description 3
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 3
- 238000002485 combustion reaction Methods 0.000 description 3
- 235000019253 formic acid Nutrition 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 239000000523 sample Substances 0.000 description 3
- DKCXIJLUMAOOHX-UHFFFAOYSA-N C(CCCCC)C(C(OC)(OC)OC)CCCCCCCC Chemical compound C(CCCCC)C(C(OC)(OC)OC)CCCCCCCC DKCXIJLUMAOOHX-UHFFFAOYSA-N 0.000 description 2
- 229920000742 Cotton Polymers 0.000 description 2
- 239000004793 Polystyrene Substances 0.000 description 2
- 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 2
- GYZLOYUZLJXAJU-UHFFFAOYSA-N diglycidyl ether Chemical compound C1OC1COCC1CO1 GYZLOYUZLJXAJU-UHFFFAOYSA-N 0.000 description 2
- HYBBIBNJHNGZAN-UHFFFAOYSA-N furfural Chemical compound O=CC1=CC=CO1 HYBBIBNJHNGZAN-UHFFFAOYSA-N 0.000 description 2
- 229910052736 halogen Inorganic materials 0.000 description 2
- 150000002367 halogens Chemical class 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 238000003760 magnetic stirring Methods 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 239000004033 plastic Substances 0.000 description 2
- 229920003023 plastic Polymers 0.000 description 2
- 229920002223 polystyrene Polymers 0.000 description 2
- OCJUKGOGIGVWBY-UHFFFAOYSA-N trioxidanylperoxymethane Chemical compound COOOOO OCJUKGOGIGVWBY-UHFFFAOYSA-N 0.000 description 2
- 238000005160 1H NMR spectroscopy Methods 0.000 description 1
- LCFVJGUPQDGYKZ-UHFFFAOYSA-N Bisphenol A diglycidyl ether Chemical compound C=1C=C(OCC2OC2)C=CC=1C(C)(C)C(C=C1)=CC=C1OCC1CO1 LCFVJGUPQDGYKZ-UHFFFAOYSA-N 0.000 description 1
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical class S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 239000002841 Lewis acid Substances 0.000 description 1
- 238000005481 NMR spectroscopy Methods 0.000 description 1
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical class OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 230000004075 alteration Effects 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 125000002178 anthracenyl group Chemical group C1(=CC=CC2=CC3=CC=CC=C3C=C12)* 0.000 description 1
- 125000003710 aryl alkyl group Chemical group 0.000 description 1
- 229910001570 bauxite Inorganic materials 0.000 description 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
- 230000033228 biological regulation Effects 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 238000006482 condensation reaction Methods 0.000 description 1
- 239000013068 control sample Substances 0.000 description 1
- XLJMAIOERFSOGZ-UHFFFAOYSA-M cyanate Chemical compound [O-]C#N XLJMAIOERFSOGZ-UHFFFAOYSA-M 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- DIOQZVSQGTUSAI-NJFSPNSNSA-N decane Chemical class CCCCCCCCC[14CH3] DIOQZVSQGTUSAI-NJFSPNSNSA-N 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 239000000446 fuel Substances 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- 150000004677 hydrates Chemical class 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 239000003999 initiator Substances 0.000 description 1
- 150000007517 lewis acids Chemical class 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 229920003986 novolac Polymers 0.000 description 1
- QUHRNYKEKIJVMR-UHFFFAOYSA-N oxane-2,3,4-trione Chemical class O=C1CCOC(=O)C1=O QUHRNYKEKIJVMR-UHFFFAOYSA-N 0.000 description 1
- 230000036284 oxygen consumption Effects 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 125000000286 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
- AQSJGOWTSHOLKH-UHFFFAOYSA-N phosphite(3-) Chemical class [O-]P([O-])[O-] AQSJGOWTSHOLKH-UHFFFAOYSA-N 0.000 description 1
- UEZVMMHDMIWARA-UHFFFAOYSA-M phosphonate Chemical compound [O-]P(=O)=O UEZVMMHDMIWARA-UHFFFAOYSA-M 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000004848 polyfunctional curative Substances 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 210000003296 saliva Anatomy 0.000 description 1
- 239000000779 smoke Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 238000007655 standard test method Methods 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 239000004575 stone Substances 0.000 description 1
- 229920002803 thermoplastic polyurethane Polymers 0.000 description 1
- 239000004634 thermosetting polymer Substances 0.000 description 1
- 125000003396 thiol group Chemical group [H]S* 0.000 description 1
- 125000003944 tolyl group Chemical group 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 239000003039 volatile agent Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- 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
- C07F9/28—Phosphorus compounds with one or more P—C bonds
- C07F9/38—Phosphonic acids [RP(=O)(OH)2]; Thiophosphonic acids ; [RP(=X1)(X2H)2(X1, X2 are each independently O, S or Se)]
- C07F9/40—Esters thereof
-
- 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
- C07F9/28—Phosphorus compounds with one or more P—C bonds
- C07F9/38—Phosphonic acids [RP(=O)(OH)2]; Thiophosphonic acids ; [RP(=X1)(X2H)2(X1, X2 are each independently O, S or Se)]
- C07F9/40—Esters thereof
- C07F9/4003—Esters thereof the acid moiety containing a substituent or a structure which is considered as characteristic
- C07F9/4006—Esters of acyclic acids which can have further substituents on alkyl
- C07F9/4012—Esters of acyclic acids which can have further substituents on alkyl substituted by B, Si, P or a metal
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
- C08G59/18—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
- C08G59/20—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the epoxy compounds used
- C08G59/22—Di-epoxy compounds
- C08G59/30—Di-epoxy compounds containing atoms other than carbon, hydrogen, oxygen and nitrogen
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
- C08G77/04—Polysiloxanes
- C08G77/22—Polysiloxanes containing silicon bound to organic groups containing atoms other than carbon, hydrogen and oxygen
- C08G77/30—Polysiloxanes containing silicon bound to organic groups containing atoms other than carbon, hydrogen and oxygen phosphorus-containing groups
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L63/00—Compositions of epoxy resins; Compositions of derivatives of epoxy resins
-
- 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
- C09K21/06—Organic materials
- C09K21/12—Organic materials containing phosphorus
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Polymers & Plastics (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Molecular Biology (AREA)
- Biochemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Silicon Polymers (AREA)
- Fireproofing Substances (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US12/263,704 US7915436B2 (en) | 2008-11-03 | 2008-11-03 | Phosphorus-containing silsesquioxane derivatives as flame retardants |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| TW201030013A true TW201030013A (en) | 2010-08-16 |
Family
ID=41402324
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| TW098137247A TW201030013A (en) | 2008-11-03 | 2009-11-03 | Phosphorus-containing silsesquioxane derivatives as flame retardants |
Country Status (13)
| Country | Link |
|---|---|
| US (1) | US7915436B2 (enExample) |
| EP (1) | EP2352742B1 (enExample) |
| JP (1) | JP5469672B2 (enExample) |
| KR (1) | KR20110093821A (enExample) |
| CN (1) | CN102264750A (enExample) |
| BR (1) | BRPI0921806A2 (enExample) |
| CA (1) | CA2742392A1 (enExample) |
| ES (1) | ES2451514T3 (enExample) |
| MX (1) | MX2011004663A (enExample) |
| PL (1) | PL2352742T3 (enExample) |
| RU (1) | RU2485129C2 (enExample) |
| TW (1) | TW201030013A (enExample) |
| WO (1) | WO2010062709A2 (enExample) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BRPI0922176A2 (pt) * | 2008-12-08 | 2018-05-22 | 3M Innovative Properties Co | retardador de chamas isento de halogenio para sistemas de resina epóxi. |
| US9255185B2 (en) | 2012-08-13 | 2016-02-09 | International Business Machines Corporation | Flame retardant fillers prepared from bridged polysilsesquioxanes |
| CN103570758A (zh) * | 2013-10-31 | 2014-02-12 | 江汉大学 | 一种阻燃改性的硅烷偶联剂及其制备方法 |
Family Cites Families (19)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2843615A (en) * | 1956-05-31 | 1958-07-15 | Gen Electric | Organophosphorus-silicon compositions |
| US3901833A (en) * | 1970-10-23 | 1975-08-26 | Ciba Geigy Corp | Hardenable epoxy resin compositions and process for making the same |
| US3816550A (en) * | 1972-10-02 | 1974-06-11 | Union Carbide Corp | Catalytic process for hydration of olefins |
| JPS60248732A (ja) * | 1984-05-22 | 1985-12-09 | Shin Etsu Chem Co Ltd | リン酸エステル基含有オルガノポリシロキサンラテツクスの製造方法 |
| DE19500253A1 (de) * | 1995-01-05 | 1996-07-11 | Wacker Chemie Gmbh | Phosphorhaltige Organosiliciumverbindungen |
| EP0747183A3 (en) * | 1995-05-25 | 1997-10-15 | Shinetsu Chemical Co | Modification of wood |
| US6362279B2 (en) * | 1996-09-27 | 2002-03-26 | The United States Of America As Represented By The Secretary Of The Air Force | Preceramic additives as fire retardants for plastics |
| US6518357B1 (en) * | 2000-10-04 | 2003-02-11 | General Electric Company | Flame retardant polycarbonate-silsesquioxane compositions, method for making and articles made thereby |
| GB0100470D0 (en) * | 2001-01-09 | 2001-02-21 | Queen Mary & Westfield College | Organopolysiloxanes containing phosphonic groups, methods for the production and use thereof |
| KR100425376B1 (ko) * | 2001-10-29 | 2004-03-30 | 국도화학 주식회사 | 인 및 실리콘 변성 난연성 에폭시수지 |
| US7405251B2 (en) * | 2002-05-16 | 2008-07-29 | Dow Corning Corporation | Flame retardant compositions |
| US7053167B2 (en) * | 2002-09-13 | 2006-05-30 | Chisso Corporation | Silsesquioxane derivative having functional group |
| US7129370B2 (en) * | 2002-09-17 | 2006-10-31 | Chisso Corporation | Silicon compound and a production process for silicon compound |
| KR101168780B1 (ko) | 2004-02-18 | 2012-07-25 | 훈츠만 어드밴스트 머티리얼스(스위처랜드) 게엠베하 | 실록산을 사용한 난연제 조성물 |
| WO2006096775A2 (en) * | 2005-03-07 | 2006-09-14 | Hybrid Plastics, Inc. | Process for assembly of poss monomers |
| DE102005056052A1 (de) * | 2005-11-24 | 2007-05-31 | Consortium für elektrochemische Industrie GmbH | Verwendung von phosphonatmodifizierten Verbindungen als Flammschutzmittel |
| US7767736B2 (en) * | 2005-12-05 | 2010-08-03 | 3M Innovative Properties Company | Flame retardant polymer composition |
| WO2007093588A1 (de) | 2006-02-17 | 2007-08-23 | Basf Se | Oligo- und polymere arylphosphonsäure-substituierte siloxane |
| CN100513411C (zh) | 2007-01-19 | 2009-07-15 | 华南理工大学 | 一种双环笼状取代倍半硅氧烷及其制备方法与应用 |
-
2008
- 2008-11-03 US US12/263,704 patent/US7915436B2/en not_active Expired - Fee Related
-
2009
- 2009-11-02 CA CA2742392A patent/CA2742392A1/en not_active Abandoned
- 2009-11-02 MX MX2011004663A patent/MX2011004663A/es active IP Right Grant
- 2009-11-02 EP EP09745261.9A patent/EP2352742B1/en not_active Not-in-force
- 2009-11-02 CN CN2009801523723A patent/CN102264750A/zh active Pending
- 2009-11-02 JP JP2011535609A patent/JP5469672B2/ja not_active Expired - Fee Related
- 2009-11-02 RU RU2011120270/04A patent/RU2485129C2/ru not_active IP Right Cessation
- 2009-11-02 PL PL09745261T patent/PL2352742T3/pl unknown
- 2009-11-02 ES ES09745261.9T patent/ES2451514T3/es active Active
- 2009-11-02 BR BRPI0921806A patent/BRPI0921806A2/pt not_active IP Right Cessation
- 2009-11-02 WO PCT/US2009/062912 patent/WO2010062709A2/en not_active Ceased
- 2009-11-02 KR KR1020117012415A patent/KR20110093821A/ko not_active Abandoned
- 2009-11-03 TW TW098137247A patent/TW201030013A/zh unknown
Also Published As
| Publication number | Publication date |
|---|---|
| RU2011120270A (ru) | 2012-11-27 |
| WO2010062709A2 (en) | 2010-06-03 |
| CA2742392A1 (en) | 2010-06-03 |
| WO2010062709A3 (en) | 2012-05-31 |
| RU2485129C2 (ru) | 2013-06-20 |
| EP2352742B1 (en) | 2013-12-25 |
| PL2352742T3 (pl) | 2014-05-30 |
| ES2451514T3 (es) | 2014-03-27 |
| BRPI0921806A2 (pt) | 2018-06-05 |
| US7915436B2 (en) | 2011-03-29 |
| MX2011004663A (es) | 2011-05-30 |
| KR20110093821A (ko) | 2011-08-18 |
| US20100113659A1 (en) | 2010-05-06 |
| EP2352742A2 (en) | 2011-08-10 |
| JP2012509847A (ja) | 2012-04-26 |
| JP5469672B2 (ja) | 2014-04-16 |
| CN102264750A (zh) | 2011-11-30 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| Yang et al. | Synthesis of a phosphorus/nitrogen-containing additive with multifunctional groups and its flame-retardant effect in epoxy resin | |
| Jin et al. | High-efficiency flame retardant behavior of bi-DOPO compound with hydroxyl group on epoxy resin | |
| Yang et al. | Synthesis of a novel flame retardant containing phosphorus, nitrogen and boron and its application in flame-retardant epoxy resin | |
| JP4119252B2 (ja) | 防炎加工剤 | |
| JP5745508B2 (ja) | Ｄｏｐｏ由来難燃性エポキシ樹脂組成物 | |
| JP5814431B2 (ja) | リン含有フェノール樹脂及びそれを含む難燃性エポキシ樹脂硬化物 | |
| Ding et al. | Preparation and properties of halogen-free flame retardant epoxy resins with phosphorus-containing siloxanes | |
| JP6509009B2 (ja) | ビスマレイミド化合物、それを含む組成物、及び硬化物 | |
| Chen et al. | Flame retardant epoxy resins from bisphenol-A epoxy cured with hyperbranched polyphosphate ester | |
| TW200524981A (en) | Halogen-free flame-retardant resin composition and prepreg and laminate using the same | |
| Luo et al. | Highly effective flame retardancy of a novel DPPA-based curing agent for DGEBA epoxy resin | |
| You et al. | Synthesis and performance of a novel nitrogen‐containing cyclic phosphate for intumescent flame retardant and its application in epoxy resin | |
| Li et al. | Phosphorus-containing flame-retardant bismaleimide resin with high mechanical properties | |
| Li et al. | Synthesis and characterization of novel phosphorous‐silicone‐nitrogen flame retardant and evaluation of its flame retardancy for epoxy thermosets | |
| Perez et al. | Novel phosphorus‐containing hardeners with tailored chemical structures for epoxy resins: Synthesis and cured resin properties | |
| Liu et al. | Synthesis of aluminum methylcyclohexylphosphinate and its use as flame retardant for epoxy resin | |
| CN107298734B (zh) | 一种本征型无卤阻燃乙烯基酯树脂及其制备方法 | |
| US7915436B2 (en) | Phosphorus-containing silsesquioxane derivatives as flame retardants | |
| TW200842138A (en) | Flame retardant crosslink agent and epoxy resin compositions free of halogen and phosphor | |
| Zhang et al. | Comparative study on flame retardancy and thermal degradation of phosphorus-and silicon-containing epoxy resin composites | |
| JP2012025800A (ja) | エポキシ樹脂組成物、及びエポキシ樹脂 | |
| TW201249908A (en) | Aluminum phosphorus acid salts as epoxy resin cure inhibitors | |
| JP5056992B1 (ja) | リン含有硬化性樹脂組成物及びその樹脂硬化物 | |
| KR101492996B1 (ko) | 인 함유 공축합 수지 및 이를 이용한 난연성 조성물 | |
| CN101302326B (zh) | 阻燃性树脂组合物 |