CN106220579B - 包含三嗪插入的金属磷酸盐的阻燃剂组合物 - Google Patents
包含三嗪插入的金属磷酸盐的阻燃剂组合物 Download PDFInfo
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- CN106220579B CN106220579B CN201610576993.6A CN201610576993A CN106220579B CN 106220579 B CN106220579 B CN 106220579B CN 201610576993 A CN201610576993 A CN 201610576993A CN 106220579 B CN106220579 B CN 106220579B
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- Prior art keywords
- melamine
- metal phosphate
- triazine
- mel
- fire retardant
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- 229910001463 metal phosphate Inorganic materials 0.000 title claims abstract description 41
- JYEUMXHLPRZUAT-UHFFFAOYSA-N 1,2,3-triazine Chemical compound C1=CN=NN=C1 JYEUMXHLPRZUAT-UHFFFAOYSA-N 0.000 title claims abstract description 21
- 238000003780 insertion Methods 0.000 title claims abstract description 20
- 230000037431 insertion Effects 0.000 title claims abstract description 19
- 239000003063 flame retardant Substances 0.000 title abstract description 26
- 229910019142 PO4 Inorganic materials 0.000 claims abstract description 67
- 229910052782 aluminium Inorganic materials 0.000 claims description 16
- 229910052725 zinc Inorganic materials 0.000 claims description 10
- 229910052791 calcium Inorganic materials 0.000 claims description 9
- 229910052749 magnesium Inorganic materials 0.000 claims description 8
- 229910052796 boron Inorganic materials 0.000 claims description 4
- 150000003921 pyrrolotriazines Chemical class 0.000 claims description 4
- 229910052710 silicon Inorganic materials 0.000 claims description 4
- 229910052684 Cerium Inorganic materials 0.000 claims description 3
- 229910052746 lanthanum Inorganic materials 0.000 claims description 3
- 229910052748 manganese Inorganic materials 0.000 claims description 3
- 229910052719 titanium Inorganic materials 0.000 claims description 3
- 229910052726 zirconium Inorganic materials 0.000 claims description 3
- 229910052787 antimony Inorganic materials 0.000 claims description 2
- 229910052802 copper Inorganic materials 0.000 claims description 2
- 229910052742 iron Inorganic materials 0.000 claims description 2
- 229910052759 nickel Inorganic materials 0.000 claims description 2
- 229910052718 tin Inorganic materials 0.000 claims description 2
- 239000000203 mixture Substances 0.000 abstract description 39
- 150000001875 compounds Chemical class 0.000 abstract description 15
- 238000002360 preparation method Methods 0.000 abstract description 8
- -1 melamine compound Chemical class 0.000 description 46
- 229920000877 Melamine resin Polymers 0.000 description 40
- 239000000047 product Substances 0.000 description 32
- 229920000642 polymer Polymers 0.000 description 31
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 23
- 239000011701 zinc Substances 0.000 description 20
- 229910052751 metal Inorganic materials 0.000 description 16
- 239000002184 metal Substances 0.000 description 16
- XPPKVPWEQAFLFU-UHFFFAOYSA-N diphosphoric acid Chemical class OP(O)(=O)OP(O)(O)=O XPPKVPWEQAFLFU-UHFFFAOYSA-N 0.000 description 15
- 235000011180 diphosphates Nutrition 0.000 description 14
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 14
- 238000000034 method Methods 0.000 description 11
- 238000010438 heat treatment Methods 0.000 description 10
- 235000021317 phosphate Nutrition 0.000 description 9
- 229910052698 phosphorus Inorganic materials 0.000 description 9
- 239000004800 polyvinyl chloride Substances 0.000 description 9
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 8
- 239000011575 calcium Substances 0.000 description 8
- 239000010452 phosphate Substances 0.000 description 8
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 8
- 229920002647 polyamide Polymers 0.000 description 8
- 229920000915 polyvinyl chloride Polymers 0.000 description 8
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- 239000004676 acrylonitrile butadiene styrene Substances 0.000 description 7
- 229920000122 acrylonitrile butadiene styrene Polymers 0.000 description 7
- 239000011777 magnesium Substances 0.000 description 7
- 239000000463 material Substances 0.000 description 7
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- 229920001587 Wood-plastic composite Polymers 0.000 description 6
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 6
- 229920001577 copolymer Polymers 0.000 description 6
- 238000000921 elemental analysis Methods 0.000 description 6
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- 239000004700 high-density polyethylene Substances 0.000 description 6
- ZTFZSHLWORMEHO-UHFFFAOYSA-A pentaaluminum;[oxido(phosphonatooxy)phosphoryl] phosphate Chemical compound [Al+3].[Al+3].[Al+3].[Al+3].[Al+3].[O-]P([O-])(=O)OP([O-])(=O)OP([O-])([O-])=O.[O-]P([O-])(=O)OP([O-])(=O)OP([O-])([O-])=O.[O-]P([O-])(=O)OP([O-])(=O)OP([O-])([O-])=O ZTFZSHLWORMEHO-UHFFFAOYSA-A 0.000 description 6
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- LRXTYHSAJDENHV-UHFFFAOYSA-H zinc phosphate Chemical compound [Zn+2].[Zn+2].[Zn+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O LRXTYHSAJDENHV-UHFFFAOYSA-H 0.000 description 6
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 5
- 229920000388 Polyphosphate Polymers 0.000 description 5
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 5
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical class OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 5
- 239000000654 additive Substances 0.000 description 5
- 239000004411 aluminium Substances 0.000 description 5
- PWZFXELTLAQOKC-UHFFFAOYSA-A dialuminum;hexamagnesium;carbonate;hexadecahydroxide;tetrahydrate Chemical compound O.O.O.O.[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Al+3].[Al+3].[O-]C([O-])=O PWZFXELTLAQOKC-UHFFFAOYSA-A 0.000 description 5
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- YSRVJVDFHZYRPA-UHFFFAOYSA-N melem Chemical compound NC1=NC(N23)=NC(N)=NC2=NC(N)=NC3=N1 YSRVJVDFHZYRPA-UHFFFAOYSA-N 0.000 description 5
- 238000002156 mixing Methods 0.000 description 5
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- 239000000243 solution Substances 0.000 description 5
- 229910000165 zinc phosphate Inorganic materials 0.000 description 5
- BTBUEUYNUDRHOZ-UHFFFAOYSA-N Borate Chemical compound [O-]B([O-])[O-] BTBUEUYNUDRHOZ-UHFFFAOYSA-N 0.000 description 4
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 4
- ZRALSGWEFCBTJO-UHFFFAOYSA-N Guanidine Chemical compound NC(N)=N ZRALSGWEFCBTJO-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
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 4
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 4
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 4
- GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 description 4
- 239000004721 Polyphenylene oxide Substances 0.000 description 4
- 239000004372 Polyvinyl alcohol Substances 0.000 description 4
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 4
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 4
- 239000002253 acid Substances 0.000 description 4
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 4
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 description 4
- 229910021502 aluminium hydroxide Inorganic materials 0.000 description 4
- 239000004927 clay Substances 0.000 description 4
- RGPUVZXXZFNFBF-UHFFFAOYSA-K diphosphonooxyalumanyl dihydrogen phosphate Chemical class [Al+3].OP(O)([O-])=O.OP(O)([O-])=O.OP(O)([O-])=O RGPUVZXXZFNFBF-UHFFFAOYSA-K 0.000 description 4
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- 150000007974 melamines Chemical class 0.000 description 4
- UEZVMMHDMIWARA-UHFFFAOYSA-M phosphonate Chemical compound [O-]P(=O)=O UEZVMMHDMIWARA-UHFFFAOYSA-M 0.000 description 4
- 235000011007 phosphoric acid Nutrition 0.000 description 4
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- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 description 3
- YZEZMSPGIPTEBA-UHFFFAOYSA-N 2-n-(4,6-diamino-1,3,5-triazin-2-yl)-1,3,5-triazine-2,4,6-triamine Chemical compound NC1=NC(N)=NC(NC=2N=C(N)N=C(N)N=2)=N1 YZEZMSPGIPTEBA-UHFFFAOYSA-N 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 3
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- DWSWCPPGLRSPIT-UHFFFAOYSA-N benzo[c][2,1]benzoxaphosphinin-6-ium 6-oxide Chemical class C1=CC=C2[P+](=O)OC3=CC=CC=C3C2=C1 DWSWCPPGLRSPIT-UHFFFAOYSA-N 0.000 description 3
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- 229910052903 pyrophyllite Inorganic materials 0.000 description 1
- 239000010453 quartz Substances 0.000 description 1
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- 238000012552 review Methods 0.000 description 1
- 239000005060 rubber Substances 0.000 description 1
- YGSDEFSMJLZEOE-UHFFFAOYSA-M salicylate Chemical compound OC1=CC=CC=C1C([O-])=O YGSDEFSMJLZEOE-UHFFFAOYSA-M 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 229910052604 silicate mineral Inorganic materials 0.000 description 1
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- 235000019698 starch Nutrition 0.000 description 1
- 239000011115 styrene butadiene Substances 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- 125000002730 succinyl group Chemical group C(CCC(=O)*)(=O)* 0.000 description 1
- IIACRCGMVDHOTQ-UHFFFAOYSA-N sulfamic acid Chemical compound NS(O)(=O)=O IIACRCGMVDHOTQ-UHFFFAOYSA-N 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- 238000004381 surface treatment Methods 0.000 description 1
- 229920001059 synthetic polymer Polymers 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 235000012222 talc Nutrition 0.000 description 1
- KUCOHFSKRZZVRO-UHFFFAOYSA-N terephthalaldehyde Chemical compound O=CC1=CC=C(C=O)C=C1 KUCOHFSKRZZVRO-UHFFFAOYSA-N 0.000 description 1
- XGFPOHQJFNFBKA-UHFFFAOYSA-B tetraaluminum;phosphonato phosphate Chemical compound [Al+3].[Al+3].[Al+3].[Al+3].[O-]P([O-])(=O)OP([O-])([O-])=O.[O-]P([O-])(=O)OP([O-])([O-])=O.[O-]P([O-])(=O)OP([O-])([O-])=O XGFPOHQJFNFBKA-UHFFFAOYSA-B 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 239000013008 thixotropic agent Substances 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- ZHXAZZQXWJJBHA-UHFFFAOYSA-N triphenylbismuthane Chemical compound C1=CC=CC=C1[Bi](C=1C=CC=CC=1)C1=CC=CC=C1 ZHXAZZQXWJJBHA-UHFFFAOYSA-N 0.000 description 1
- 235000011178 triphosphate Nutrition 0.000 description 1
- WUUHFRRPHJEEKV-UHFFFAOYSA-N tripotassium borate Chemical compound [K+].[K+].[K+].[O-]B([O-])[O-] WUUHFRRPHJEEKV-UHFFFAOYSA-N 0.000 description 1
- BIKXLKXABVUSMH-UHFFFAOYSA-N trizinc;diborate Chemical compound [Zn+2].[Zn+2].[Zn+2].[O-]B([O-])[O-].[O-]B([O-])[O-] BIKXLKXABVUSMH-UHFFFAOYSA-N 0.000 description 1
- 229920000785 ultra high molecular weight polyethylene Polymers 0.000 description 1
- 229920001862 ultra low molecular weight polyethylene Polymers 0.000 description 1
- 150000003672 ureas Chemical class 0.000 description 1
- 210000002700 urine Anatomy 0.000 description 1
- 229920001866 very low density polyethylene Polymers 0.000 description 1
- 239000000052 vinegar Substances 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 239000010456 wollastonite Substances 0.000 description 1
- 229910052882 wollastonite Inorganic materials 0.000 description 1
- OMSYGYSPFZQFFP-UHFFFAOYSA-J zinc pyrophosphate Chemical compound [Zn+2].[Zn+2].[O-]P([O-])(=O)OP([O-])([O-])=O OMSYGYSPFZQFFP-UHFFFAOYSA-J 0.000 description 1
- CZPRKINNVBONSF-UHFFFAOYSA-M zinc;dioxido(oxo)phosphanium Chemical compound [Zn+2].[O-][P+]([O-])=O CZPRKINNVBONSF-UHFFFAOYSA-M 0.000 description 1
- BNEMLSQAJOPTGK-UHFFFAOYSA-N zinc;dioxido(oxo)tin Chemical compound [Zn+2].[O-][Sn]([O-])=O BNEMLSQAJOPTGK-UHFFFAOYSA-N 0.000 description 1
- 229910000166 zirconium phosphate Inorganic materials 0.000 description 1
- LEHFSLREWWMLPU-UHFFFAOYSA-B zirconium(4+);tetraphosphate Chemical compound [Zr+4].[Zr+4].[Zr+4].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O LEHFSLREWWMLPU-UHFFFAOYSA-B 0.000 description 1
Classifications
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D251/00—Heterocyclic compounds containing 1,3,5-triazine rings
- C07D251/02—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings
- C07D251/12—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
- C07D251/26—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with only hetero atoms directly attached to ring carbon atoms
- C07D251/40—Nitrogen atoms
- C07D251/54—Three nitrogen atoms
-
- 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
- C09K21/14—Macromolecular materials
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D251/00—Heterocyclic compounds containing 1,3,5-triazine rings
- C07D251/02—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings
- C07D251/12—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
- C07D251/26—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with only hetero atoms directly attached to ring carbon atoms
- C07D251/40—Nitrogen atoms
- C07D251/54—Three nitrogen atoms
- C07D251/56—Preparation of melamine
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D251/00—Heterocyclic compounds containing 1,3,5-triazine rings
- C07D251/02—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings
- C07D251/12—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
- C07D251/26—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with only hetero atoms directly attached to ring carbon atoms
- C07D251/40—Nitrogen atoms
- C07D251/54—Three nitrogen atoms
- C07D251/70—Other substituted melamines
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/12—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains three hetero rings
- C07D487/16—Peri-condensed systems
-
- 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
- C07F9/657172—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 one oxygen atom being part of a (thio)phosphinic acid ester: (X = O, S)
-
- 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
- C08G79/00—Macromolecular compounds obtained by reactions forming a linkage containing atoms other than silicon, sulfur, nitrogen, oxygen, and carbon with or without the latter elements in the main chain of the macromolecule
- C08G79/02—Macromolecular compounds obtained by reactions forming a linkage containing atoms other than silicon, sulfur, nitrogen, oxygen, and carbon with or without the latter elements in the main chain of the macromolecule a linkage containing phosphorus
-
- 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
- C08G79/00—Macromolecular compounds obtained by reactions forming a linkage containing atoms other than silicon, sulfur, nitrogen, oxygen, and carbon with or without the latter elements in the main chain of the macromolecule
- C08G79/02—Macromolecular compounds obtained by reactions forming a linkage containing atoms other than silicon, sulfur, nitrogen, oxygen, and carbon with or without the latter elements in the main chain of the macromolecule a linkage containing phosphorus
- C08G79/04—Phosphorus linked to oxygen or to oxygen and carbon
-
- 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
- C08K13/00—Use of mixtures of ingredients not covered by one single of the preceding main groups, each of these compounds being essential
- C08K13/02—Organic and inorganic ingredients
-
- 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
- C08K5/0091—Complexes with metal-heteroatom-bonds
-
- 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
- C08K5/5205—Salts of P-acids with N-bases
-
- 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
- C08K5/5313—Phosphinic compounds, e.g. R2=P(:O)OR'
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Life Sciences & Earth Sciences (AREA)
- Molecular Biology (AREA)
- General Health & Medical Sciences (AREA)
- Biochemistry (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Fireproofing Substances (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE102010035103.2 | 2010-08-23 | ||
| DE102010035103A DE102010035103A1 (de) | 2010-08-23 | 2010-08-23 | Flammschutzmittelzusammensetzungen enthaltend Triazin-interkalierte Metall-Phosphate |
| CN201180041164.3A CN103201355B (zh) | 2010-08-23 | 2011-08-05 | 包含三嗪插入的金属磷酸盐的阻燃剂组合物 |
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| CN201610576993.6A Active CN106220579B (zh) | 2010-08-23 | 2011-08-05 | 包含三嗪插入的金属磷酸盐的阻燃剂组合物 |
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| DE102010035103A1 (de) * | 2010-08-23 | 2012-02-23 | Catena Additives Gmbh & Co. Kg | Flammschutzmittelzusammensetzungen enthaltend Triazin-interkalierte Metall-Phosphate |
| KR20150042159A (ko) * | 2012-07-17 | 2015-04-20 | 이탈마치 케미칼스 에스피에이 | Pvc 난연성 조성물 |
| KR101828892B1 (ko) * | 2012-10-16 | 2018-02-13 | 제이. 엠. 후버 코포레이션 | 난연제 재료로서의 아진 금속 포스페이트 |
| TWI472553B (zh) * | 2012-12-20 | 2015-02-11 | Taiwan Textile Res Inst | 阻燃耐隆共聚物及其纖維 |
| DE102013210902A1 (de) | 2013-02-13 | 2014-08-14 | Floridienne S.A. | Flammschutzmittelzusammensetzung |
| CN103193226A (zh) * | 2013-05-02 | 2013-07-10 | 哈尔滨工业大学 | 一种阻燃可膨胀石墨的制备方法 |
| CN103819682B (zh) * | 2014-01-23 | 2016-03-09 | 苏州大学 | 一种膨胀型阻燃剂、合成方法及其应用 |
| US10035896B2 (en) * | 2014-07-29 | 2018-07-31 | Lanxess Solutions Us Inc. | Salts of pyrophosphonic acid as flame retardants |
| CN105623677A (zh) * | 2014-10-27 | 2016-06-01 | 武汉凌科达科技有限公司 | 一种无卤阻燃组合物 |
| CN105623676A (zh) * | 2014-10-27 | 2016-06-01 | 武汉凌科达科技有限公司 | 一种无卤阻燃组合物的制备方法 |
| DE202014009839U1 (de) | 2014-12-11 | 2016-03-15 | Lanxess Deutschland Gmbh | Flammgeschützte Faser-Matrix-Halbzeuge |
| WO2016104512A1 (ja) * | 2014-12-26 | 2016-06-30 | 新日鐵住金株式会社 | 電磁鋼板 |
| CN104552488A (zh) * | 2015-01-12 | 2015-04-29 | 信阳美丽真好秸秆新材科技有限公司 | 阻燃复合板及其制造方法 |
| EP3067388A1 (de) | 2015-03-09 | 2016-09-14 | LANXESS Deutschland GmbH | Thermoplastische formmassen |
| ES2905876T3 (es) | 2015-03-09 | 2022-04-12 | Lanxess Deutschland Gmbh | Masas de moldeo termoplásticas |
| DE102015009598A1 (de) | 2015-07-24 | 2017-01-26 | Trupti Dave-Wehner | Verfahren zur Herstellung eines halogenfreien Flammschutzmittels |
| CN108350137B (zh) | 2015-11-13 | 2020-10-23 | 爱思乐-艾博美国有限公司 | 聚氨酯和聚异氰脲酸酯泡沫用的反应性阻燃剂 |
| CN105820375A (zh) * | 2016-05-23 | 2016-08-03 | 徐州猎奇商贸有限公司 | 一种复合阻燃剂 |
| EP3257893B1 (de) | 2016-06-15 | 2018-12-26 | LANXESS Deutschland GmbH | Faser-matrix-halbzeug |
| SE539718C2 (en) * | 2016-06-21 | 2017-11-07 | Pp Polymer Ab | Flame retardant additive for polymers |
| EP3290469A1 (de) | 2016-09-01 | 2018-03-07 | LANXESS Deutschland GmbH | Thermoplastische formmassen |
| EP3290475A1 (de) | 2016-09-01 | 2018-03-07 | LANXESS Deutschland GmbH | Thermoplastische formmassen |
| CN106519736B (zh) * | 2016-09-12 | 2018-06-22 | 华南理工大学 | 兼具催化成炭和自由基猝灭功能纳米磷酸锆及其制备方法与应用 |
| RU2637955C1 (ru) * | 2016-12-20 | 2017-12-08 | Федеральное государственное бюджетное образовательное учреждение высшего образования "Волгоградский государственный технический университет" (ВолгГТУ) | Фторсодержащая полиамидная композиция с пониженной горючестью |
| WO2019055325A2 (en) | 2017-09-12 | 2019-03-21 | Biocapital Holdings, Llc | BIOOGICAL DEVICES AND METHODS OF USING THE SAME TO PRODUCE STEVIOL GLYCOSIDES |
| CN107828267B (zh) * | 2017-11-02 | 2020-03-31 | 合众（佛山）化工有限公司 | 一种硅硼改性自阻燃型水性涂料 |
| CN107936297A (zh) * | 2017-11-22 | 2018-04-20 | 江苏利思德新材料有限公司 | 玻纤增强尼龙用无卤阻燃复配体系及其在无卤阻燃玻纤增强尼龙材料中的应用 |
| CN108410012B (zh) * | 2018-03-15 | 2020-04-07 | 西南大学 | 一种高效阻燃纳米协效剂及其制备方法和应用 |
| CN108211516B (zh) * | 2018-03-23 | 2020-05-26 | 兰州石化职业技术学院 | 一种负载胺沸石复合助滤剂的制备方法 |
| CN108410074A (zh) * | 2018-04-19 | 2018-08-17 | 滁州君越高分子新材料有限公司 | 一种环保型阻燃胶管的配方 |
| RU2716448C1 (ru) * | 2019-06-06 | 2020-03-11 | Общество с ограниченной ответственностью "Химиндустрия-Инвест" | Огнезащитная интумесцентная краска с увеличенным пределом огнестойкости |
| EP4010450A4 (en) * | 2019-08-09 | 2023-05-03 | Daihachi Chemical Industry Co., Ltd. | FLAME RETARDANT COMPOSITION AND FLAME RETARDANT THERMOPLASTIC POLYURETHANE COMPOSITION |
| CN111100303B (zh) * | 2019-12-02 | 2020-11-17 | 厦门大学 | 一种有机膦接枝中空金属有机框架材料的制备方法及其应用 |
| MX2022013022A (es) | 2020-04-24 | 2022-11-07 | Huber Corp J M | Metodos para la polimerizacion continua de compuestos de fosfato para formar composiciones de polifosfato. |
| CN111635714A (zh) * | 2020-06-22 | 2020-09-08 | 袁志伟 | 一种木质人造板环保高效抑烟添加型阻燃剂 |
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| CN112063015A (zh) * | 2020-09-30 | 2020-12-11 | 广东顺亨新材料有限公司 | 一种尼龙用无卤阻燃母粒及其制备方法 |
| WO2022086010A1 (ko) * | 2020-10-22 | 2022-04-28 | 영남대학교 산학협력단 | 결정성이 억제된 인산염을 이용한 고분자 가공용 열안정제 및 이의 제조방법 |
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| CN112280102A (zh) * | 2020-11-11 | 2021-01-29 | 云南锡业集团（控股）有限责任公司研发中心 | 一种仿生合成技术制备锡基复合阻燃剂的方法 |
| CN115505186A (zh) * | 2021-06-23 | 2022-12-23 | 南京工程学院 | 一种含三聚氰胺间接插层g-C3N4的阻燃电缆料及其制备方法 |
| CN114015060B (zh) * | 2021-12-07 | 2022-11-22 | 什邡市长丰化工有限公司 | 一种聚磷酸铵阻燃剂、其制备方法及应用 |
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Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20040082697A1 (en) * | 2000-12-15 | 2004-04-29 | Raetzsch Manfred | Modified inorganic particles |
| DE102007036465A1 (de) * | 2007-08-01 | 2009-02-05 | Catena Additives Gmbh & Co. Kg | Phosphorhaltige Triazin-Verbindungen als Flammschutzmittel |
Family Cites Families (50)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4714724A (en) * | 1980-05-05 | 1987-12-22 | Stauffer Chemical Company | Dibromoneopentyl phosphate melamine salt flame retardant |
| US4373103A (en) * | 1980-05-05 | 1983-02-08 | Stauffer Chemical Company | Dibromoneopentyl phosphate melamine salt flame retardant |
| ES270928Y (es) | 1982-03-17 | 1986-04-01 | Bomba hidraulica perfeccionada. | |
| DE4001805A1 (de) * | 1990-01-23 | 1991-07-25 | Sueddeutsche Kalkstickstoff | Verfahren zur herstellung von cyanamid |
| DE4023310A1 (de) * | 1990-07-21 | 1992-01-23 | Bayer Ag | Intumeszenztraeger und deren verwendung |
| JP3505836B2 (ja) | 1995-03-30 | 2004-03-15 | 東ソー株式会社 | 難燃性樹脂組成物 |
| EP0754728A1 (de) * | 1995-07-14 | 1997-01-22 | Hoechst Aktiengesellschaft | Flammwidrige Epoxidharz-Formmassen |
| JP3804084B2 (ja) | 1995-07-28 | 2006-08-02 | 東ソー株式会社 | エチレンジアミンリン酸亜鉛、その製造方法及びそれを用いた難燃性樹脂組成物 |
| JP3744045B2 (ja) | 1995-09-26 | 2006-02-08 | 東ソー株式会社 | ジエチレントリアミン含有リン酸亜鉛及びその製造方法、並びにそれを用いた難燃剤及び難燃性樹脂組成物 |
| JP3700295B2 (ja) | 1996-07-22 | 2005-09-28 | 東ソー株式会社 | 難燃剤及びそれを配合してなる難燃性樹脂組成物 |
| JP3718947B2 (ja) | 1997-03-18 | 2005-11-24 | 東ソー株式会社 | 難燃剤及び難燃性樹脂組成物 |
| JPH11152373A (ja) | 1997-11-25 | 1999-06-08 | Tosoh Corp | 成形性及び熱安定性に優れた非ハロゲン系難燃樹脂組成物 |
| US6207735B1 (en) | 1997-12-08 | 2001-03-27 | Tosch Corporation | Flame retardant and flame retardant resin composition containing it |
| JPH11269187A (ja) | 1997-12-08 | 1999-10-05 | Tosoh Corp | エチレンジアミンリン酸亜鉛、その製造方法、及びそれを配合してなる難燃性樹脂組成物 |
| JPH11199708A (ja) | 1998-01-12 | 1999-07-27 | Tosoh Corp | 表面処理されたエチレンジアミンリン酸亜鉛、及びそれを配合してなる難燃性樹脂組成物 |
| JP3991422B2 (ja) | 1998-03-02 | 2007-10-17 | 東ソー株式会社 | ポリオール組成物、難燃性ポリウレタン樹脂組成物及びそれらの製造法 |
| JPH11293155A (ja) | 1998-04-09 | 1999-10-26 | Tosoh Corp | 耐火塗料 |
| NL1009588C2 (nl) | 1998-07-08 | 2000-01-11 | Dsm Nv | Polyfosfaatzout van een 1,3,5-triazineverbinding met hoge condensatiegraad, een werkwijze voor de bereiding ervan en de toepassing als vlamdover in polymeersamenstellingen. |
| JP2000063562A (ja) | 1998-08-12 | 2000-02-29 | Tosoh Corp | 表面処理されたポリリン酸アンモニウム及びそれを含有した難燃性樹脂組成物 |
| JP2000063563A (ja) | 1998-08-12 | 2000-02-29 | Tosoh Corp | ポリイソシアネート化合物で表面処理されたポリリン酸アンモニウム及びそれを含有した難燃性樹脂組成物 |
| KR100503978B1 (ko) * | 1998-08-24 | 2005-07-27 | 니폰 가가쿠 고교 가부시키가이샤 | 난연제 조성물 및 난연성 수지 조성물 |
| JP2000154283A (ja) | 1998-11-20 | 2000-06-06 | Tosoh Corp | 柔軟性のある難燃性樹脂組成物 |
| JP2000154287A (ja) | 1998-11-20 | 2000-06-06 | Tosoh Corp | 耐水性に優れた難燃性樹脂組成物 |
| JP2000154324A (ja) | 1998-11-20 | 2000-06-06 | Tosoh Corp | 熱安定性の良好な難燃性樹脂組成物 |
| BR0007830A (pt) | 1999-01-28 | 2002-01-15 | Vantico Ag | Silicatos em camada modificados por melamina |
| DE19903709A1 (de) | 1999-01-30 | 2000-08-10 | Clariant Gmbh | Flammschutzmittel-Kombination für thermoplastische Polymere II |
| NL1011631C2 (nl) * | 1999-03-22 | 2000-09-27 | Dsm Nv | Vlamdovende samenstelling en werkwijze voor de bereiding ervan. |
| JP2001011462A (ja) | 1999-06-30 | 2001-01-16 | Tosoh Corp | ピペラジン骨格を含むアミン含有リン酸亜鉛からなる難燃剤、及びそれを配合してなる難燃性樹脂組成物 |
| JP2001031408A (ja) | 1999-07-19 | 2001-02-06 | Tosoh Corp | エチレンジアミンリン酸亜鉛マグネシウム、その製造方法及びそれを配合してなる難燃性樹脂組成物 |
| JP4007911B2 (ja) * | 2000-08-30 | 2007-11-14 | 旭化成エレクトロニクス株式会社 | 硬化性樹脂組成物 |
| DE10100591A1 (de) * | 2001-01-09 | 2002-07-11 | Bayer Ag | Phosphorhaltiges Flammschutzmittel und Flammwidrige thermoplastische Formmassen |
| US6737456B2 (en) | 2001-02-27 | 2004-05-18 | Bromine Compounds Ltd. | Fire-retardant polyolefin compositions |
| JP2002322322A (ja) * | 2001-02-27 | 2002-11-08 | Bromine Compounds Ltd | 難燃性ポリオレフィン組成物 |
| EP1434767A1 (en) * | 2001-10-09 | 2004-07-07 | Ciba SC Holding AG | Halogen-free flame retardant compounds |
| JP2003226819A (ja) * | 2001-11-30 | 2003-08-15 | Polyplastics Co | 難燃性樹脂組成物 |
| CN1329482C (zh) * | 2002-06-24 | 2007-08-01 | 株式会社艾迪科 | 阻燃剂组合物以及含有该组合物的阻燃性树脂组合物 |
| DE602005016235D1 (de) * | 2004-04-01 | 2009-10-08 | Sabic Innovative Plastics Ip | Flammschutzmittelzusammensetzung |
| ATE446339T1 (de) * | 2005-06-23 | 2009-11-15 | Catena Additives Gmbh & Co Kg | Koordinationspolymere triethanolaminperchlorato (triflato)-metall-innerkomplexe als additive für synthetische polymere |
| KR100773734B1 (ko) | 2006-12-29 | 2007-11-09 | 제일모직주식회사 | 난연성이 우수한 열가소성 폴리에스테르 수지 조성물 |
| KR101472608B1 (ko) | 2007-04-03 | 2014-12-16 | 바스프 에스이 | Ｄｏｐｏ 난연제 조성물 |
| US9200122B2 (en) * | 2007-08-01 | 2015-12-01 | J. M. Huber Corporation | Triazine compounds containing phosphorous as flame retardants |
| MX2010002529A (es) | 2007-09-13 | 2010-03-25 | Basf Se | Combinaciones de retardadores de flama de oxidos de hidroxialquil fosfina con 1, 3, 5-triazinas y epoxidos. |
| KR20090067663A (ko) * | 2007-12-21 | 2009-06-25 | 루브리졸 어드밴스드 머티어리얼스, 인코포레이티드 | 비할로겐 난연 열가소성 폴리우레탄 복합 수지 조성물 |
| DE102008016964A1 (de) * | 2008-03-31 | 2009-10-01 | Ami Agrolinz Melamine International Gmbh | Verfahren zur Herstellung einer Verbindung mit mindestens einer zumindest einfach substituierten Aminogruppe |
| DE102008016967A1 (de) * | 2008-03-31 | 2009-10-01 | Ami Agrolinz Melamine International Gmbh | Verfahren zur Herstellung einer Verbindung mit mindestens einer zumindest einfach substituierten Aminogruppe |
| CN102224219A (zh) | 2008-11-24 | 2011-10-19 | 巴斯夫欧洲公司 | 蜜胺苯基次膦酸盐阻燃剂组合物 |
| EP2373728A1 (en) | 2008-12-04 | 2011-10-12 | Basf Se | Melamine phenylphosphonate flame retardant compositions |
| DE102010035103A1 (de) * | 2010-08-23 | 2012-02-23 | Catena Additives Gmbh & Co. Kg | Flammschutzmittelzusammensetzungen enthaltend Triazin-interkalierte Metall-Phosphate |
| KR101828892B1 (ko) * | 2012-10-16 | 2018-02-13 | 제이. 엠. 후버 코포레이션 | 난연제 재료로서의 아진 금속 포스페이트 |
| DE102013210902A1 (de) * | 2013-02-13 | 2014-08-14 | Floridienne S.A. | Flammschutzmittelzusammensetzung |
-
2010
- 2010-08-23 DE DE102010035103A patent/DE102010035103A1/de not_active Ceased
-
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- 2011-08-05 RU RU2013112675/05A patent/RU2580733C2/ru active
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Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20040082697A1 (en) * | 2000-12-15 | 2004-04-29 | Raetzsch Manfred | Modified inorganic particles |
| DE102007036465A1 (de) * | 2007-08-01 | 2009-02-05 | Catena Additives Gmbh & Co. Kg | Phosphorhaltige Triazin-Verbindungen als Flammschutzmittel |
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