KR100720873B1 - 비스페놀-ａ 비스(디페닐 포스페이트)-기재 방염제 - Google Patents
비스페놀-ａ 비스(디페닐 포스페이트)-기재 방염제 Download PDFInfo
- Publication number
- KR100720873B1 KR100720873B1 KR1020017015969A KR20017015969A KR100720873B1 KR 100720873 B1 KR100720873 B1 KR 100720873B1 KR 1020017015969 A KR1020017015969 A KR 1020017015969A KR 20017015969 A KR20017015969 A KR 20017015969A KR 100720873 B1 KR100720873 B1 KR 100720873B1
- Authority
- KR
- South Korea
- Prior art keywords
- bisphenol
- area
- flame retardant
- diphenyl phosphate
- bis
- Prior art date
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- 239000003063 flame retardant Substances 0.000 title claims abstract description 51
- 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 39
- 229910019142 PO4 Inorganic materials 0.000 title description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 title description 2
- 239000010452 phosphate Substances 0.000 title description 2
- BQPNUOYXSVUVMY-UHFFFAOYSA-N [4-[2-(4-diphenoxyphosphoryloxyphenyl)propan-2-yl]phenyl] diphenyl phosphate Chemical compound C=1C=C(OP(=O)(OC=2C=CC=CC=2)OC=2C=CC=CC=2)C=CC=1C(C)(C)C(C=C1)=CC=C1OP(=O)(OC=1C=CC=CC=1)OC1=CC=CC=C1 BQPNUOYXSVUVMY-UHFFFAOYSA-N 0.000 claims abstract description 36
- 238000004128 high performance liquid chromatography Methods 0.000 claims abstract description 20
- 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 abstract description 12
- WLXXENAUDPZXIB-UHFFFAOYSA-N diphenyl (2-prop-1-en-2-ylphenyl) phosphate Chemical compound CC(=C)C1=CC=CC=C1OP(=O)(OC=1C=CC=CC=1)OC1=CC=CC=C1 WLXXENAUDPZXIB-UHFFFAOYSA-N 0.000 claims abstract description 7
- 239000000203 mixture Substances 0.000 claims description 21
- 229920005989 resin Polymers 0.000 claims description 11
- 239000011347 resin Substances 0.000 claims description 11
- 239000007788 liquid Substances 0.000 claims description 10
- XECAHXYUAAWDEL-UHFFFAOYSA-N acrylonitrile butadiene styrene Chemical compound C=CC=C.C=CC#N.C=CC1=CC=CC=C1 XECAHXYUAAWDEL-UHFFFAOYSA-N 0.000 claims description 6
- 229920000122 acrylonitrile butadiene styrene Polymers 0.000 claims description 6
- 239000004676 acrylonitrile butadiene styrene Substances 0.000 claims description 6
- 239000004417 polycarbonate Substances 0.000 claims description 6
- 239000004721 Polyphenylene oxide Substances 0.000 claims description 5
- 229920006380 polyphenylene oxide Polymers 0.000 claims description 5
- 229920000515 polycarbonate Polymers 0.000 claims description 4
- 239000004793 Polystyrene Substances 0.000 claims 1
- 229920002223 polystyrene Polymers 0.000 claims 1
- 229920005992 thermoplastic resin Polymers 0.000 claims 1
- 239000000539 dimer Substances 0.000 abstract description 27
- ASMQGLCHMVWBQR-UHFFFAOYSA-M diphenyl phosphate Chemical compound C=1C=CC=CC=1OP(=O)([O-])OC1=CC=CC=C1 ASMQGLCHMVWBQR-UHFFFAOYSA-M 0.000 abstract 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 64
- RLOWWWKZYUNIDI-UHFFFAOYSA-N phosphinic chloride Chemical compound ClP=O RLOWWWKZYUNIDI-UHFFFAOYSA-N 0.000 description 30
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 28
- 229940106691 bisphenol a Drugs 0.000 description 26
- 238000006243 chemical reaction Methods 0.000 description 25
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 18
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 18
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 17
- 239000012535 impurity Substances 0.000 description 17
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 17
- 238000000034 method Methods 0.000 description 16
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 15
- 239000003054 catalyst Substances 0.000 description 10
- UAEPNZWRGJTJPN-UHFFFAOYSA-N methylcyclohexane Chemical compound CC1CCCCC1 UAEPNZWRGJTJPN-UHFFFAOYSA-N 0.000 description 10
- 239000013638 trimer Substances 0.000 description 10
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 9
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 9
- 238000004821 distillation Methods 0.000 description 9
- 229910052757 nitrogen Inorganic materials 0.000 description 9
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 8
- 239000000178 monomer Substances 0.000 description 8
- 239000012071 phase Substances 0.000 description 8
- 239000000376 reactant Substances 0.000 description 8
- 238000005481 NMR spectroscopy Methods 0.000 description 7
- 238000009472 formulation Methods 0.000 description 7
- 239000008346 aqueous phase Substances 0.000 description 6
- NUHSROFQTUXZQQ-UHFFFAOYSA-N isopentenyl diphosphate Chemical compound CC(=C)CCO[P@](O)(=O)OP(O)(O)=O NUHSROFQTUXZQQ-UHFFFAOYSA-N 0.000 description 6
- 239000012074 organic phase Substances 0.000 description 6
- 239000000243 solution Substances 0.000 description 6
- 238000005406 washing Methods 0.000 description 6
- 239000003518 caustics Substances 0.000 description 5
- 238000002425 crystallisation Methods 0.000 description 5
- 230000008025 crystallization Effects 0.000 description 5
- -1 isopropenylphenyl diphenylphosphate Chemical compound 0.000 description 5
- GYNNXHKOJHMOHS-UHFFFAOYSA-N methyl-cycloheptane Natural products CC1CCCCCC1 GYNNXHKOJHMOHS-UHFFFAOYSA-N 0.000 description 5
- 239000011574 phosphorus Substances 0.000 description 5
- 229910052698 phosphorus Inorganic materials 0.000 description 5
- 239000000047 product Substances 0.000 description 5
- 239000011541 reaction mixture Substances 0.000 description 5
- 230000002829 reductive effect Effects 0.000 description 5
- 239000002904 solvent Substances 0.000 description 5
- 239000008399 tap water Substances 0.000 description 5
- 235000020679 tap water Nutrition 0.000 description 5
- 238000004458 analytical method Methods 0.000 description 4
- 239000012043 crude product Substances 0.000 description 4
- 239000007787 solid Substances 0.000 description 4
- AYEKOFBPNLCAJY-UHFFFAOYSA-O thiamine pyrophosphate Chemical compound CC1=C(CCOP(O)(=O)OP(O)(O)=O)SC=[N+]1CC1=CN=C(C)N=C1N AYEKOFBPNLCAJY-UHFFFAOYSA-O 0.000 description 4
- TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 239000013078 crystal Substances 0.000 description 3
- 150000002148 esters Chemical class 0.000 description 3
- 229920005669 high impact polystyrene Polymers 0.000 description 3
- 239000004797 high-impact polystyrene Substances 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 239000003960 organic solvent Substances 0.000 description 3
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 2
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- 230000002411 adverse Effects 0.000 description 2
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 239000012467 final product Substances 0.000 description 2
- 238000002347 injection Methods 0.000 description 2
- 239000007924 injection Substances 0.000 description 2
- 230000014759 maintenance of location Effects 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 229910001510 metal chloride Inorganic materials 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- 238000005191 phase separation Methods 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 230000035484 reaction time Effects 0.000 description 2
- 239000012925 reference material Substances 0.000 description 2
- 239000013557 residual solvent Substances 0.000 description 2
- 238000003860 storage Methods 0.000 description 2
- 238000000825 ultraviolet detection Methods 0.000 description 2
- 239000008096 xylene Substances 0.000 description 2
- JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 description 2
- WUQYBSRMWWRFQH-UHFFFAOYSA-N 2-prop-1-en-2-ylphenol Chemical compound CC(=C)C1=CC=CC=C1O WUQYBSRMWWRFQH-UHFFFAOYSA-N 0.000 description 1
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- 239000004609 Impact Modifier Substances 0.000 description 1
- 239000012963 UV stabilizer Substances 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000002528 anti-freeze Effects 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- 125000001246 bromo group Chemical group Br* 0.000 description 1
- 239000001110 calcium chloride Substances 0.000 description 1
- 229910001628 calcium chloride Inorganic materials 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 239000002826 coolant Substances 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- RCJVRSBWZCNNQT-UHFFFAOYSA-N dichloridooxygen Chemical compound ClOCl RCJVRSBWZCNNQT-UHFFFAOYSA-N 0.000 description 1
- MQHNKCZKNAJROC-UHFFFAOYSA-N dipropyl phthalate Chemical compound CCCOC(=O)C1=CC=CC=C1C(=O)OCCC MQHNKCZKNAJROC-UHFFFAOYSA-N 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000009977 dual effect Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000010828 elution Methods 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 235000011389 fruit/vegetable juice Nutrition 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 239000013067 intermediate product Substances 0.000 description 1
- 230000000670 limiting effect Effects 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- 229910001629 magnesium chloride Inorganic materials 0.000 description 1
- 239000012046 mixed solvent Substances 0.000 description 1
- 210000003097 mucus Anatomy 0.000 description 1
- 230000003472 neutralizing effect Effects 0.000 description 1
- CMPQUABWPXYYSH-UHFFFAOYSA-N phenyl phosphate Chemical compound OP(O)(=O)OC1=CC=CC=C1 CMPQUABWPXYYSH-UHFFFAOYSA-N 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920001707 polybutylene terephthalate Polymers 0.000 description 1
- 239000002952 polymeric resin Substances 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 239000011342 resin composition Substances 0.000 description 1
- 230000000979 retarding effect Effects 0.000 description 1
- 230000002441 reversible effect Effects 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- XJDNKRIXUMDJCW-UHFFFAOYSA-J titanium tetrachloride Chemical compound Cl[Ti](Cl)(Cl)Cl XJDNKRIXUMDJCW-UHFFFAOYSA-J 0.000 description 1
- 238000005292 vacuum distillation Methods 0.000 description 1
- 238000010792 warming Methods 0.000 description 1
- 239000003643 water by type Substances 0.000 description 1
- 239000011592 zinc chloride Substances 0.000 description 1
- 235000005074 zinc chloride Nutrition 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
- C08K5/52—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
- 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 System
- C07F9/02—Phosphorus compounds
- C07F9/06—Phosphorus compounds without P—C bonds
- C07F9/08—Esters of oxyacids of phosphorus
- C07F9/09—Esters of phosphoric acids
- C07F9/12—Esters of phosphoric acids with hydroxyaryl compounds
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US09/330,688 | 1999-06-11 | ||
| US09/330,688 US6319432B1 (en) | 1999-06-11 | 1999-06-11 | Bisphenol-A bis(diphenyl phosphate)-based flame retardant |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| KR20020010927A KR20020010927A (ko) | 2002-02-06 |
| KR100720873B1 true KR100720873B1 (ko) | 2007-05-22 |
Family
ID=23290873
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1020017015969A KR100720873B1 (ko) | 1999-06-11 | 2000-06-06 | 비스페놀-ａ 비스(디페닐 포스페이트)-기재 방염제 |
Country Status (6)
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2768837A4 (en) * | 2011-10-21 | 2015-06-03 | Perstorp Ab | NOVEL PHOSPHATE COMPOUNDS BASED ON TETRAOXASPIRO [5.5] UNDECAN AND THEIR USE AS FLAME RETARDANTS |
Families Citing this family (34)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP3926938B2 (ja) * | 1998-12-03 | 2007-06-06 | 三菱エンジニアリングプラスチックス株式会社 | 難燃性ポリカーボネート樹脂組成物 |
| DE10036057A1 (de) * | 2000-07-25 | 2002-02-07 | Bayer Ag | Flammwidrige Polycarbonat-Zusammensetzungen |
| US6399685B1 (en) * | 2000-12-11 | 2002-06-04 | Albemarle Corporation | Purification of arylene polyphosphate esters |
| DE10100591A1 (de) * | 2001-01-09 | 2002-07-11 | Bayer Ag | Phosphorhaltiges Flammschutzmittel und Flammwidrige thermoplastische Formmassen |
| US7303810B2 (en) * | 2001-03-05 | 2007-12-04 | 3Form, Inc. | Fire-resistant architectural resin materials |
| US7691470B2 (en) * | 2001-03-05 | 2010-04-06 | 3Form | Laminate structure with polycarbonate sheets |
| US7008700B1 (en) | 2001-03-05 | 2006-03-07 | 3-Form | Architectural laminate panel with embedded compressible objects and methods for making the same |
| US6667355B2 (en) * | 2001-08-30 | 2003-12-23 | Pabu Services, Inc. | Higher alkylated triaryl phosphate ester flame retardants |
| DE10216736A1 (de) * | 2002-04-16 | 2004-02-05 | Bayer Ag | Flammschutzmittel für Polymere enthaltend eine Mischung aus zwei verschiedenen Arylphosphaten, deren Herstellung und deren Verwendung |
| CN1708503A (zh) * | 2002-10-26 | 2005-12-14 | 阿克苏诺贝尔公司 | 低聚磷酸酯组合物结晶的延迟 |
| US20060046017A1 (en) | 2004-09-01 | 2006-03-02 | 3Form | Architectural glass panels with embedded objects and methods for making the same |
| US20060068317A1 (en) * | 2004-09-30 | 2006-03-30 | Klei Steven R | Poly(arylene ether) composition |
| WO2007056456A1 (en) * | 2005-11-08 | 2007-05-18 | Supresta Llc | Flame retardant composition and hydrolysis-susceptible resin containing same |
| US20070254991A1 (en) * | 2006-04-28 | 2007-11-01 | Saadat Hussain | Phosphorus-containing tetrabromobisphenol A |
| TW200813197A (en) * | 2006-07-07 | 2008-03-16 | Albemarle Corp | Phosphorous-based flame retardant recovery method |
| BRPI0811211A8 (pt) | 2007-05-08 | 2016-04-26 | 3Form Inc | Sistema de cor multivariado com aplicação de textura |
| US8968611B2 (en) * | 2008-06-09 | 2015-03-03 | Adeka Corporation | Process for solidification of phosphoric ester-based flame retardants |
| CN101348500B (zh) * | 2008-08-19 | 2012-02-22 | 山东默锐化学有限公司 | 一种双酚a双(二苯基磷酸酯)的制备方法 |
| KR101013666B1 (ko) * | 2008-09-18 | 2011-02-10 | 한밭대학교 산학협력단 | 컴퓨터용 방열장치 |
| EP2358816B1 (en) * | 2008-12-08 | 2021-03-24 | SABIC Global Technologies B.V. | Flame retardant polycarbonate compositions, method of manufacture thereof, and articles therefrom |
| WO2011054862A1 (de) | 2009-11-05 | 2011-05-12 | Bayer Materialscience Ag | Platten aus polycarbonat mit verbesserter flammwidrigkeit |
| TWI382988B (zh) * | 2009-12-25 | 2013-01-21 | Grand Tek Advance Material Science Co Ltd | 有機矽磷酸酯及其製作方法 |
| CN101831308A (zh) * | 2010-04-19 | 2010-09-15 | 江苏大明科技有限公司 | 一种高分子量固体磷酸酯阻燃剂及其制备方法和应用 |
| CN101993586B (zh) * | 2010-11-30 | 2012-10-10 | 金发科技股份有限公司 | 一种阻燃的聚碳酸酯/abs材料 |
| TWI410446B (zh) | 2011-01-05 | 2013-10-01 | Grand Tek Advance Material Science Co Ltd | 含磷酚醛樹脂與其形成方法及含磷配方 |
| USD691289S1 (en) | 2012-09-05 | 2013-10-08 | 3Form, Inc. | Panel with cut and aligned thatch interlayer |
| CN104829647B (zh) * | 2014-04-10 | 2016-08-24 | 北京理工阻燃科技有限公司 | 一种含磷聚醚酯的制备方法及应用 |
| US10240030B2 (en) * | 2014-12-02 | 2019-03-26 | Sabic Global Technologies B.V. | Article comprising a high flow polyetherimide composition |
| JP6532276B2 (ja) * | 2015-04-23 | 2019-06-19 | 株式会社Adeka | 難燃性水系ポリウレタン樹脂組成物、及びそれを塗布してなる難燃性ポリエステル系繊維 |
| CN104962059B (zh) * | 2015-06-18 | 2016-11-02 | 金发科技股份有限公司 | 一种聚碳酸酯组合物及其制备方法 |
| CN106699805B (zh) * | 2016-12-15 | 2019-02-01 | 衢州普信新材料有限公司 | 一种双酚a双（二苯基磷酸酯）的制备方法 |
| CN108676282A (zh) * | 2018-05-18 | 2018-10-19 | 武汉理工大学 | 一种环保阻燃型pvc/abs合金及其制备方法 |
| CN111040457B (zh) * | 2019-12-27 | 2022-05-06 | 广东精一塑胶实业有限公司 | 一种用于塑料的固化包覆阻燃防水剂的制备方法 |
| CN112142779B (zh) * | 2020-10-13 | 2023-01-13 | 中国科学院宁波材料技术与工程研究所 | 一种双酚a双(磷酸二芳酯)的快速制备方法 |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1997047361A1 (en) * | 1996-06-12 | 1997-12-18 | Southwest Research Institute | Fire extinguishing trash can liner |
| WO1998004566A1 (en) * | 1996-07-29 | 1998-02-05 | Akzo Nobel N.V. | Process for the formation of hydrocarbyl bis(dihydrocarbyl phosphate) |
| WO1998035790A1 (de) * | 1997-02-17 | 1998-08-20 | Bessey & Sohn Gmbh & Co. | Spanneinrichtung |
Family Cites Families (37)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2520090A (en) | 1947-12-30 | 1950-08-22 | Monsanto Chemicals | Polyphosphates of divalent aryl hydrocarbons |
| GB734767A (en) | 1952-01-10 | 1955-08-10 | Lankro Chem Ltd | New neutral orthophosphate esters |
| US3174931A (en) | 1961-12-05 | 1965-03-23 | Sinclair Research Inc | Grease compositions |
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- 1999-06-11 US US09/330,688 patent/US6319432B1/en not_active Expired - Fee Related
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- 2000-06-06 WO PCT/US2000/015598 patent/WO2000077012A1/en active Search and Examination
- 2000-06-06 EP EP00939617A patent/EP1194435A1/en not_active Withdrawn
- 2000-06-06 CN CNB008087938A patent/CN1210284C/zh not_active Expired - Fee Related
- 2000-06-06 JP JP2001503869A patent/JP2003502451A/ja not_active Withdrawn
- 2000-06-06 KR KR1020017015969A patent/KR100720873B1/ko not_active IP Right Cessation
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| WO1997047361A1 (en) * | 1996-06-12 | 1997-12-18 | Southwest Research Institute | Fire extinguishing trash can liner |
| WO1998004566A1 (en) * | 1996-07-29 | 1998-02-05 | Akzo Nobel N.V. | Process for the formation of hydrocarbyl bis(dihydrocarbyl phosphate) |
| WO1998035790A1 (de) * | 1997-02-17 | 1998-08-20 | Bessey & Sohn Gmbh & Co. | Spanneinrichtung |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2768837A4 (en) * | 2011-10-21 | 2015-06-03 | Perstorp Ab | NOVEL PHOSPHATE COMPOUNDS BASED ON TETRAOXASPIRO [5.5] UNDECAN AND THEIR USE AS FLAME RETARDANTS |
Also Published As
| Publication number | Publication date |
|---|---|
| CN1355808A (zh) | 2002-06-26 |
| CN1210284C (zh) | 2005-07-13 |
| JP2003502451A (ja) | 2003-01-21 |
| WO2000077012A1 (en) | 2000-12-21 |
| EP1194435A1 (en) | 2002-04-10 |
| US6319432B1 (en) | 2001-11-20 |
| KR20020010927A (ko) | 2002-02-06 |
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