CN109233160A - A kind of organic silicon fibre retardant and preparation method thereof containing PTFE and nano silica - Google Patents
A kind of organic silicon fibre retardant and preparation method thereof containing PTFE and nano silica Download PDFInfo
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- CN109233160A CN109233160A CN201811056120.8A CN201811056120A CN109233160A CN 109233160 A CN109233160 A CN 109233160A CN 201811056120 A CN201811056120 A CN 201811056120A CN 109233160 A CN109233160 A CN 109233160A
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- dispersing agent
- monomer
- weight ratio
- phenyl
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- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 title claims abstract description 83
- 229910052710 silicon Inorganic materials 0.000 title claims abstract description 74
- 239000010703 silicon Substances 0.000 title claims abstract description 74
- 239000000835 fiber Substances 0.000 title claims abstract description 73
- 239000004810 polytetrafluoroethylene Substances 0.000 title claims abstract description 73
- 229920001343 polytetrafluoroethylene Polymers 0.000 title claims abstract description 73
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 title claims abstract description 72
- 238000002360 preparation method Methods 0.000 title claims abstract description 51
- 239000000377 silicon dioxide Substances 0.000 title claims abstract description 40
- 239000000178 monomer Substances 0.000 claims abstract description 144
- 239000005416 organic matter Substances 0.000 claims abstract description 54
- 239000006210 lotion Substances 0.000 claims abstract description 47
- 229920001296 polysiloxane Polymers 0.000 claims abstract description 40
- 230000015572 biosynthetic process Effects 0.000 claims abstract description 28
- 238000003786 synthesis reaction Methods 0.000 claims abstract description 27
- 238000005253 cladding Methods 0.000 claims abstract description 25
- 238000002156 mixing Methods 0.000 claims abstract description 18
- -1 cyclic siloxane Chemical class 0.000 claims description 209
- 239000000203 mixture Substances 0.000 claims description 144
- 239000002270 dispersing agent Substances 0.000 claims description 91
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 claims description 90
- 239000000839 emulsion Substances 0.000 claims description 72
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 57
- 229920000515 polycarbonate Polymers 0.000 claims description 56
- 239000004417 polycarbonate Substances 0.000 claims description 55
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 50
- 239000003795 chemical substances by application Substances 0.000 claims description 47
- 239000003995 emulsifying agent Substances 0.000 claims description 47
- 239000002245 particle Substances 0.000 claims description 46
- 229910000019 calcium carbonate Inorganic materials 0.000 claims description 45
- 229920002521 macromolecule Polymers 0.000 claims description 44
- 239000003063 flame retardant Substances 0.000 claims description 42
- 239000006185 dispersion Substances 0.000 claims description 40
- 239000007788 liquid Substances 0.000 claims description 38
- 239000003999 initiator Substances 0.000 claims description 34
- 238000003756 stirring Methods 0.000 claims description 33
- 229910052757 nitrogen Inorganic materials 0.000 claims description 32
- 125000005375 organosiloxane group Chemical group 0.000 claims description 32
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 28
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 claims description 28
- 239000003054 catalyst Substances 0.000 claims description 28
- 239000000463 material Substances 0.000 claims description 28
- 239000000243 solution Substances 0.000 claims description 28
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 27
- 229920003171 Poly (ethylene oxide) Polymers 0.000 claims description 26
- 150000003242 quaternary ammonium salts Chemical class 0.000 claims description 26
- 238000006243 chemical reaction Methods 0.000 claims description 23
- RRAFCDWBNXTKKO-UHFFFAOYSA-N eugenol Chemical compound COC1=CC(CC=C)=CC=C1O RRAFCDWBNXTKKO-UHFFFAOYSA-N 0.000 claims description 23
- NOKUWSXLHXMAOM-UHFFFAOYSA-N hydroxy(phenyl)silicon Chemical compound O[Si]C1=CC=CC=C1 NOKUWSXLHXMAOM-UHFFFAOYSA-N 0.000 claims description 23
- 125000001820 oxy group Chemical group [*:1]O[*:2] 0.000 claims description 23
- 239000000843 powder Substances 0.000 claims description 23
- 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 claims description 22
- 239000002253 acid Substances 0.000 claims description 22
- 239000003365 glass fiber Substances 0.000 claims description 22
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 22
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 claims description 21
- 239000006087 Silane Coupling Agent Substances 0.000 claims description 21
- 150000001408 amides Chemical class 0.000 claims description 21
- 229920006150 hyperbranched polyester Polymers 0.000 claims description 21
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 claims description 20
- 239000012752 auxiliary agent Substances 0.000 claims description 20
- 229910000077 silane Inorganic materials 0.000 claims description 20
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 20
- 229920002554 vinyl polymer Polymers 0.000 claims description 20
- 238000010792 warming Methods 0.000 claims description 20
- 239000000779 smoke Substances 0.000 claims description 19
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 claims description 18
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 18
- 229920000402 bisphenol A polycarbonate polymer Polymers 0.000 claims description 17
- 239000002994 raw material Substances 0.000 claims description 17
- 239000003963 antioxidant agent Substances 0.000 claims description 16
- 230000003078 antioxidant effect Effects 0.000 claims description 16
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 16
- 239000004205 dimethyl polysiloxane Substances 0.000 claims description 16
- 235000013870 dimethyl polysiloxane Nutrition 0.000 claims description 16
- 239000000194 fatty acid Substances 0.000 claims description 16
- 229930195729 fatty acid Natural products 0.000 claims description 16
- 239000000314 lubricant Substances 0.000 claims description 16
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 claims description 16
- 150000001335 aliphatic alkanes Chemical class 0.000 claims description 15
- 239000007787 solid Substances 0.000 claims description 15
- KBPLFHHGFOOTCA-UHFFFAOYSA-N 1-Octanol Chemical compound CCCCCCCCO KBPLFHHGFOOTCA-UHFFFAOYSA-N 0.000 claims description 14
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 claims description 14
- 239000003093 cationic surfactant Substances 0.000 claims description 14
- 239000012153 distilled water Substances 0.000 claims description 14
- 238000001035 drying Methods 0.000 claims description 14
- 239000000155 melt Substances 0.000 claims description 14
- 239000002736 nonionic surfactant Substances 0.000 claims description 14
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 claims description 14
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 14
- 239000002002 slurry Substances 0.000 claims description 14
- 238000010189 synthetic method Methods 0.000 claims description 14
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 claims description 14
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 claims description 14
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 13
- 150000002148 esters Chemical class 0.000 claims description 13
- 229920006322 acrylamide copolymer Polymers 0.000 claims description 11
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 11
- 239000003921 oil Substances 0.000 claims description 10
- LVXLKXRFAQXSLE-UHFFFAOYSA-N 2-[6-(2-hydroxyphenyl)hexyl]phenol Chemical compound C1(=C(C=CC=C1)CCCCCCC1=C(C=CC=C1)O)O LVXLKXRFAQXSLE-UHFFFAOYSA-N 0.000 claims description 9
- 229920003086 cellulose ether Polymers 0.000 claims description 9
- 238000005660 chlorination reaction Methods 0.000 claims description 9
- 239000001257 hydrogen Substances 0.000 claims description 9
- 229910052739 hydrogen Inorganic materials 0.000 claims description 9
- 229920013636 polyphenyl ether polymer Polymers 0.000 claims description 9
- 241000894007 species Species 0.000 claims description 9
- SFVFIFLLYFPGHH-UHFFFAOYSA-M stearalkonium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCCCC[N+](C)(C)CC1=CC=CC=C1 SFVFIFLLYFPGHH-UHFFFAOYSA-M 0.000 claims description 9
- XDLMVUHYZWKMMD-UHFFFAOYSA-N 3-trimethoxysilylpropyl 2-methylprop-2-enoate Chemical compound CO[Si](OC)(OC)CCCOC(=O)C(C)=C XDLMVUHYZWKMMD-UHFFFAOYSA-N 0.000 claims description 8
- 239000003945 anionic surfactant Substances 0.000 claims description 8
- 125000005504 styryl group Chemical group 0.000 claims description 8
- OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 claims description 7
- SJECZPVISLOESU-UHFFFAOYSA-N 3-trimethoxysilylpropan-1-amine Chemical compound CO[Si](OC)(OC)CCCN SJECZPVISLOESU-UHFFFAOYSA-N 0.000 claims description 7
- GYCMBHHDWRMZGG-UHFFFAOYSA-N Methylacrylonitrile Chemical compound CC(=C)C#N GYCMBHHDWRMZGG-UHFFFAOYSA-N 0.000 claims description 7
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 claims description 7
- IAXXETNIOYFMLW-COPLHBTASA-N [(1s,3s,4s)-4,7,7-trimethyl-3-bicyclo[2.2.1]heptanyl] 2-methylprop-2-enoate Chemical compound C1C[C@]2(C)[C@@H](OC(=O)C(=C)C)C[C@H]1C2(C)C IAXXETNIOYFMLW-COPLHBTASA-N 0.000 claims description 7
- 238000013019 agitation Methods 0.000 claims description 7
- XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 claims description 7
- 239000007864 aqueous solution Substances 0.000 claims description 7
- 239000007844 bleaching agent Substances 0.000 claims description 7
- 229910052799 carbon Inorganic materials 0.000 claims description 7
- 239000007795 chemical reaction product Substances 0.000 claims description 7
- YQHLDYVWEZKEOX-UHFFFAOYSA-N cumene hydroperoxide Chemical compound OOC(C)(C)C1=CC=CC=C1 YQHLDYVWEZKEOX-UHFFFAOYSA-N 0.000 claims description 7
- 244000144992 flock Species 0.000 claims description 7
- 239000001530 fumaric acid Substances 0.000 claims description 7
- 238000010438 heat treatment Methods 0.000 claims description 7
- 229940119545 isobornyl methacrylate Drugs 0.000 claims description 7
- 235000006408 oxalic acid Nutrition 0.000 claims description 7
- 229910052697 platinum Inorganic materials 0.000 claims description 7
- 238000009938 salting Methods 0.000 claims description 7
- 229920005573 silicon-containing polymer Polymers 0.000 claims description 7
- GCLGEJMYGQKIIW-UHFFFAOYSA-H sodium hexametaphosphate Chemical compound [Na]OP1(=O)OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])O1 GCLGEJMYGQKIIW-UHFFFAOYSA-H 0.000 claims description 7
- 239000000725 suspension Substances 0.000 claims description 7
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 claims description 7
- 238000005406 washing Methods 0.000 claims description 7
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 claims description 6
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 claims description 6
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 claims description 6
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 claims description 6
- AYJRCSIUFZENHW-UHFFFAOYSA-L barium carbonate Chemical compound [Ba+2].[O-]C([O-])=O AYJRCSIUFZENHW-UHFFFAOYSA-L 0.000 claims description 6
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 6
- 229920002678 cellulose Polymers 0.000 claims description 6
- 239000001913 cellulose Substances 0.000 claims description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 claims description 6
- 229920005615 natural polymer Polymers 0.000 claims description 6
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims description 6
- 150000003891 oxalate salts Chemical class 0.000 claims description 6
- 239000002244 precipitate Substances 0.000 claims description 6
- 150000003467 sulfuric acid derivatives Chemical class 0.000 claims description 6
- 238000001291 vacuum drying Methods 0.000 claims description 6
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 5
- 239000005977 Ethylene Substances 0.000 claims description 5
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical group C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 5
- 229920001577 copolymer Polymers 0.000 claims description 5
- 108090000623 proteins and genes Proteins 0.000 claims description 5
- 102000004169 proteins and genes Human genes 0.000 claims description 5
- 229920002153 Hydroxypropyl cellulose Polymers 0.000 claims description 4
- 229920006243 acrylic copolymer Polymers 0.000 claims description 4
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 claims description 4
- 239000001863 hydroxypropyl cellulose Substances 0.000 claims description 4
- 235000010977 hydroxypropyl cellulose Nutrition 0.000 claims description 4
- 238000006116 polymerization reaction Methods 0.000 claims description 4
- 239000005995 Aluminium silicate Substances 0.000 claims description 3
- 241001474374 Blennius Species 0.000 claims description 3
- 108010028690 Fish Proteins Proteins 0.000 claims description 3
- 108010010803 Gelatin Proteins 0.000 claims description 3
- 239000004354 Hydroxyethyl cellulose Substances 0.000 claims description 3
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 claims description 3
- 239000004372 Polyvinyl alcohol Substances 0.000 claims description 3
- 229920002472 Starch Polymers 0.000 claims description 3
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 claims description 3
- 238000006136 alcoholysis reaction Methods 0.000 claims description 3
- 125000003342 alkenyl group Chemical group 0.000 claims description 3
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 claims description 3
- 229910021502 aluminium hydroxide Inorganic materials 0.000 claims description 3
- 235000012211 aluminium silicate Nutrition 0.000 claims description 3
- 239000000440 bentonite Substances 0.000 claims description 3
- 229910000278 bentonite Inorganic materials 0.000 claims description 3
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 claims description 3
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 claims description 3
- 239000000920 calcium hydroxide Substances 0.000 claims description 3
- 229910001861 calcium hydroxide Inorganic materials 0.000 claims description 3
- QXDMQSPYEZFLGF-UHFFFAOYSA-L calcium oxalate Chemical compound [Ca+2].[O-]C(=O)C([O-])=O QXDMQSPYEZFLGF-UHFFFAOYSA-L 0.000 claims description 3
- 150000001720 carbohydrates Chemical class 0.000 claims description 3
- 235000014633 carbohydrates Nutrition 0.000 claims description 3
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 claims description 3
- 229920000159 gelatin Polymers 0.000 claims description 3
- 239000008273 gelatin Substances 0.000 claims description 3
- 235000019322 gelatine Nutrition 0.000 claims description 3
- 235000011852 gelatine desserts Nutrition 0.000 claims description 3
- 239000003292 glue Substances 0.000 claims description 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 3
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 claims description 3
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 claims description 3
- ZLNQQNXFFQJAID-UHFFFAOYSA-L magnesium carbonate Chemical compound [Mg+2].[O-]C([O-])=O ZLNQQNXFFQJAID-UHFFFAOYSA-L 0.000 claims description 3
- 239000001095 magnesium carbonate Substances 0.000 claims description 3
- 229910000021 magnesium carbonate Inorganic materials 0.000 claims description 3
- VTHJTEIRLNZDEV-UHFFFAOYSA-L magnesium dihydroxide Chemical compound [OH-].[OH-].[Mg+2] VTHJTEIRLNZDEV-UHFFFAOYSA-L 0.000 claims description 3
- 239000000347 magnesium hydroxide Substances 0.000 claims description 3
- 229910001862 magnesium hydroxide Inorganic materials 0.000 claims description 3
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 3
- 229920000609 methyl cellulose Polymers 0.000 claims description 3
- 239000001923 methylcellulose Substances 0.000 claims description 3
- PZNOBXVHZYGUEX-UHFFFAOYSA-N n-prop-2-enylprop-2-en-1-amine;hydrochloride Chemical compound Cl.C=CCNCC=C PZNOBXVHZYGUEX-UHFFFAOYSA-N 0.000 claims description 3
- 230000003647 oxidation Effects 0.000 claims description 3
- 238000007254 oxidation reaction Methods 0.000 claims description 3
- 239000001814 pectin Substances 0.000 claims description 3
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- 229920002451 polyvinyl alcohol Polymers 0.000 claims description 3
- 229920000036 polyvinylpyrrolidone Polymers 0.000 claims description 3
- 239000001267 polyvinylpyrrolidone Substances 0.000 claims description 3
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 claims description 3
- 125000005401 siloxanyl group Chemical group 0.000 claims description 3
- 239000008107 starch Substances 0.000 claims description 3
- 235000019698 starch Nutrition 0.000 claims description 3
- 239000000454 talc Substances 0.000 claims description 3
- 235000012222 talc Nutrition 0.000 claims description 3
- 229910052623 talc Inorganic materials 0.000 claims description 3
- 239000004408 titanium dioxide Substances 0.000 claims description 3
- 239000011787 zinc oxide Substances 0.000 claims description 3
- 230000008859 change Effects 0.000 claims description 2
- 125000000392 cycloalkenyl group Chemical group 0.000 claims description 2
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 2
- 150000001721 carbon Chemical group 0.000 claims 2
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims 1
- 241000556074 Grindelia camporum Species 0.000 claims 1
- 150000001412 amines Chemical class 0.000 claims 1
- 229910021529 ammonia Inorganic materials 0.000 claims 1
- JJTDIRSCDLGMRU-UHFFFAOYSA-N azane;prop-2-enamide Chemical compound N.NC(=O)C=C JJTDIRSCDLGMRU-UHFFFAOYSA-N 0.000 claims 1
- 229910052791 calcium Inorganic materials 0.000 claims 1
- 239000011575 calcium Substances 0.000 claims 1
- GJYLKIZKRHDRER-UHFFFAOYSA-N calcium;sulfuric acid Chemical compound [Ca].OS(O)(=O)=O GJYLKIZKRHDRER-UHFFFAOYSA-N 0.000 claims 1
- HRYZWHHZPQKTII-UHFFFAOYSA-N chloroethane Chemical compound CCCl HRYZWHHZPQKTII-UHFFFAOYSA-N 0.000 claims 1
- KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical class [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 claims 1
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- 238000002844 melting Methods 0.000 claims 1
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- 238000000034 method Methods 0.000 abstract description 8
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- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 24
- 235000019441 ethanol Nutrition 0.000 description 23
- JGWUKKFNKOUBPW-UHFFFAOYSA-N 2-ethenyl-1,3,5,7,2,4,6,8-tetraoxatetrasilocane Chemical class C=C[SiH]1O[SiH2]O[SiH2]O[SiH2]O1 JGWUKKFNKOUBPW-UHFFFAOYSA-N 0.000 description 11
- 230000000694 effects Effects 0.000 description 10
- IHRMXHHFNOEOEA-UHFFFAOYSA-N 2-phenyl-1,3,5,7,2,4,6,8-tetraoxatetrasilocane Chemical compound C1(=CC=CC=C1)[SiH]1O[SiH2]O[SiH2]O[SiH2]O1 IHRMXHHFNOEOEA-UHFFFAOYSA-N 0.000 description 9
- 235000019198 oils Nutrition 0.000 description 9
- XGMDYIYCKWMWLY-UHFFFAOYSA-N 2,2,2-trifluoroethanesulfonic acid Chemical compound OS(=O)(=O)CC(F)(F)F XGMDYIYCKWMWLY-UHFFFAOYSA-N 0.000 description 8
- DETXZQGDWUJKMO-UHFFFAOYSA-N 2-hydroxymethanesulfonic acid Chemical compound OCS(O)(=O)=O DETXZQGDWUJKMO-UHFFFAOYSA-N 0.000 description 8
- ZMWJQGOYIBHQJG-UHFFFAOYSA-N 3-[diethoxy(methyl)silyl]propan-1-ol Chemical compound CCO[Si](C)(OCC)CCCO ZMWJQGOYIBHQJG-UHFFFAOYSA-N 0.000 description 8
- WQPMYSHJKXVTME-UHFFFAOYSA-N 3-hydroxypropane-1-sulfonic acid Chemical compound OCCCS(O)(=O)=O WQPMYSHJKXVTME-UHFFFAOYSA-N 0.000 description 8
- RBIILJCATVGHHI-UHFFFAOYSA-N [diethoxy(phenyl)silyl]methanamine Chemical compound NC[Si](OCC)(OCC)C1=CC=CC=C1 RBIILJCATVGHHI-UHFFFAOYSA-N 0.000 description 8
- YBHBEZSZXFLQMW-UHFFFAOYSA-N [dimethoxy(phenyl)silyl]methanamine Chemical compound CO[Si](CN)(OC)C1=CC=CC=C1 YBHBEZSZXFLQMW-UHFFFAOYSA-N 0.000 description 8
- 238000013329 compounding Methods 0.000 description 8
- JJRDHFIVAPVZJN-UHFFFAOYSA-N cyclotrisiloxane Chemical compound O1[SiH2]O[SiH2]O[SiH2]1 JJRDHFIVAPVZJN-UHFFFAOYSA-N 0.000 description 8
- 239000001301 oxygen Substances 0.000 description 8
- 229910052760 oxygen Inorganic materials 0.000 description 8
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- 239000002341 toxic gas Substances 0.000 description 1
- QQQSFSZALRVCSZ-UHFFFAOYSA-N triethoxysilane Chemical compound CCO[SiH](OCC)OCC QQQSFSZALRVCSZ-UHFFFAOYSA-N 0.000 description 1
- JRSJRHKJPOJTMS-MDZDMXLPSA-N trimethoxy-[(e)-2-phenylethenyl]silane Chemical compound CO[Si](OC)(OC)\C=C\C1=CC=CC=C1 JRSJRHKJPOJTMS-MDZDMXLPSA-N 0.000 description 1
- DXZMANYCMVCPIM-UHFFFAOYSA-L zinc;diethylphosphinate Chemical compound [Zn+2].CCP([O-])(=O)CC.CCP([O-])(=O)CC DXZMANYCMVCPIM-UHFFFAOYSA-L 0.000 description 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L27/00—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 a halogen; Compositions of derivatives of such polymers
- C08L27/02—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 a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L27/12—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 a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment containing fluorine atoms
- C08L27/18—Homopolymers or copolymers or tetrafluoroethene
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- 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
- C08L25/16—Homopolymers or copolymers of alkyl-substituted styrenes
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L69/00—Compositions of polycarbonates; Compositions of derivatives of polycarbonates
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L83/00—Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon only; Compositions of derivatives of such polymers
- C08L83/04—Polysiloxanes
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- 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
- C08K2201/00—Specific properties of additives
- C08K2201/011—Nanostructured additives
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- 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
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2205/00—Polymer mixtures characterised by other features
- C08L2205/03—Polymer mixtures characterised by other features containing three or more polymers in a blend
- C08L2205/035—Polymer mixtures characterised by other features containing three or more polymers in a blend containing four or more polymers in a blend
Abstract
The present invention relates to pluronic polymer technical fields, and in particular to a kind of organic silicon fibre retardant and preparation method thereof containing PTFE and nano silica, which includes: Nano-meter SiO_22Surface it is modified;The synthesis of organopolysiloxane core lotion;Hydridization organic matter/Nano-meter SiO_22The preparation of lotion;The preparation of organic silicon fibre retardant containing PTFE and nanosized SiO_2.Preparation method of the invention is by by organic matter and Nano-meter SiO_22Hydridization is added cladding monomer and is coated, the organic silicon fibre retardant containing PTFE and nano silica, simple process and low cost is made after mixing with PTFE.
Description
Technical field
The present invention relates to pluronic polymer technical fields, and in particular to a kind of organosilicon containing PTFE and nano silica
Fire retardant and preparation method thereof.
Background technique
Traditional organic silicon fibre retardant is a kind of new and effective, less toxic, anti-molten drop, environmental-friendly halogen-free flame retardants,
It is a kind of charcoal becoming smoke suppressant.Organic silicon fibre retardant is assigning except the excellent flame retardant property of substrate, moreover it is possible to improve adding for substrate
Work performance, heat resistance etc..
But still further aspect, for organic silicon fibre retardant due to being high molecular polymer, high temperature resistant decomposition temperature is still lower;
In application process, it is also desirable to add a certain amount of anti-dripping agent and be used in compounding.
Summary of the invention
In order to overcome shortcoming and defect existing in the prior art, the purpose of the present invention is to provide one kind containing PTFE and to receive
The preparation method of the organic silicon fibre retardant of rice silica, the preparation method is by by organic matter and Nano-meter SiO_22Hydridization, with
Cladding monomer is added after PTFE mixing to be coated, the organic silicon fibre retardant containing PTFE and nano silica, technique letter is made
It is single, it is at low cost.
Another object of the present invention is to provide a kind of organic silicon fibre retardant containing PTFE and nano silica, the machine silicon
The resistance to thermal decomposition temperature of organic silicon fibre retardant had not only can be improved in fire retardant, but also fire retardant is made to have anti-dripping effects, had also improved
The flame retardant property of machine silicon fire retardant.
The purpose of the invention is achieved by the following technical solution: a kind of organic silicon flame-retardant containing PTFE and nano silica
The preparation method of agent, includes the following steps:
A, Nano-meter SiO_22Surface it is modified:
A1, configuration ethanol/water solution, are added Nano-meter SiO_22Particle, the high speed shear under the revolving speed of 3000-4000rpm;Its
In, the volume ratio of ethyl alcohol and water is 3-10:1, Nano-meter SiO_22The dosage of particle is the 0.1%-10% of ethanol/water solution quality;
A2, silane coupling agent is added, adding oxalic acid solution makes the pH value of reaction system in 3-4, after reacting 1.5-2.5h,
It filters, washing, the Nano-meter SiO_2 modified up to surface after dry2Particle;Wherein, the dosage of silane coupling agent is Nano-meter SiO_22Particle
The 1%-10% of quality;
B, the synthesis of organopolysiloxane core lotion:
Organosiloxane monomer is uniformly mixed, is added in the aqueous solution dissolved with catalyst and emulsifier, 30~
5~10h is reacted at a temperature of 80 DEG C, obtains organopolysiloxane core lotion;Wherein, the gross mass of organosiloxane monomer is water quality
The 40%~60% of amount, the dosage of catalyst are the 1%~5% of organosiloxane monomer mass, and the dosage of emulsifier is organic
The 1%~20% of siloxanyl monomers quality;
C, hydridization organic matter/Nano-meter SiO_22The preparation of lotion:
C1, it takes emulsifier soluble in water, the Nano-meter SiO_2 modified by surface is added2Particle disperses 10- using ultrasonic wave
30min obtains dispersion liquid;Wherein, the dosage of emulsifier is the 1%~20% of water quality, by the modified Nano-meter SiO_2 in surface2
The dosage of particle is the 0.1%-10% of water quality;
C2, then dispersion liquid is added in organopolysiloxane core lotion, cladding monomer and initiator is added, caused poly-
Reaction is closed, hydridization organic matter/Nano-meter SiO_2 is obtained2Lotion;Wherein, the dosage of dispersion liquid is organopolysiloxane core quality of the emulsion
10%-50%, the dosage for coating monomer is the 30%-70% of organopolysiloxane core quality of the emulsion, and the dosage of initiator is
The 0.1%-0.8% of organopolysiloxane core quality of the emulsion;
D, contain PTFE and Nano-meter SiO_22Organic silicon fibre retardant preparation:
D1, by hydridization organic matter/Nano-meter SiO_22Lotion, PTFE emulsion, dispersing agent and distilled water are added to reaction kettle together
In, 5~25min of high shear agitation under 1000~2000rpm revolving speed;Wherein, the dosage of PTFE emulsion be hydridization organic matter/
Nano-meter SiO_22The 10%-50% of quality of the emulsion, the dosage of dispersing agent are hydridization organic matter/Nano-meter SiO_22The 1%- of quality of the emulsion
5%;
D2, cladding monomer is added, adds emulsifier and initiator, reacts 6-10h at a temperature of 50~80 DEG C;Wherein,
The dosage for coating monomer is hydridization organic matter/Nano-meter SiO_22The 30%-70% of quality of the emulsion, the dosage of emulsifier are that hydridization is organic
Object/Nano-meter SiO_22The 1%~20% of quality of the emulsion, the dosage of initiator are hydridization organic matter/Nano-meter SiO_22Quality of the emulsion
0.1%-0.8%;
D3, reaction product washed, is centrifuged, drying drying, the having containing PTFE and nano silica is made
Machine silicon fire retardant.
Wherein, in the step A2, silane coupling agent is by 3- aminopropyl trimethoxysilane, three (beta-methoxy of vinyl
Base oxethyl) silane and γ-methacryloxypropyl trimethoxy silane formed with weight ratio 2-4:1.5-2.5:1 it is mixed
Close object.The present invention passes through type, compounding and the proportion of strict control silane coupling agent, can be to Nano-meter SiO_22Surface is carried out to change
Property, improve Nano-meter SiO_22With the compatibility of resin, the intensity and heat resistance of resin can also be improved.
Preferably, in the step B, organosiloxane monomer be by phenyl siloxane monomer, cyclic siloxane monomer and
The mixture that vinylsiloxane monomer is formed with weight ratio 4-8:2-6:0.1-1.0.
The present invention is by using phenyl siloxane monomer, cyclic siloxane monomer and vinylsiloxane monomer as organic
Siloxanyl monomers are used in compounding, and controlling its weight ratio is 4-8:2-6:0.1-1.0, and anti-flammability, the waterproof of resin can be improved
Property, grease proofness, anti-fog properties, soil resistance, soil release performance, moisture-proof, lubricity, abrasion performance, antistick characteristic, chemical resistance and resistance to
It is scratch resistance.
The structural formula of the phenyl siloxane monomer are as follows:Wherein, R1、R2、R3And R4Respectively hydrogen, first
Any one in base, ethyl, propyl, vinyl, acrylic, acetenyl, propinyl, methoxyl group, ethyoxyl and phenyl, and
R1、R2、R3And R4In at least one be phenyl, at least one methoxy or ethoxy.
Preferably, the phenyl siloxane monomer is phenyltrimethoxysila,e, dimethoxydiphenylsilane, triphenyl
Methoxy silane, aminomethyl phenyl dimethoxysilane, ethylphenyl dimethoxysilane, propyl phenyidimethoxysilane, second
Alkenyl phenyidimethoxysilane, acrylic phenyidimethoxysilane, ethynyl phenyl dimethoxysilane, propinyl phenyl
Dimethoxysilane, methyldiphenyl methoxylsilane, ethyl diphenyl methoxy silane, propyl diphenylmethyl oxysilane,
Vinyl diphenyl methoxy silane, acrylic diphenylmethyl oxysilane, acetenyl diphenylmethyl oxysilane, propinyl two
Phenylmethoxysilane, dimethyl benzene methoxylsilane, diethylbenzene methoxylsilane, dipropyl Phenylmethoxy silicon
Alkane, divinyl phenylmethoxysilane, diallyl phenylmethoxysilane, diacetylene phenylmethoxysilane, dipropyl
Alkynyl phenyl methoxy silane, Methylethyl phenylmethoxysilane, methyl-propyl phenylmethoxysilane, ethyl propyl phenyl
Methoxy silane, methyl vinyl phenyl methoxy silane, ethyl propylene base phenylmethoxysilane, methylacetylenyl phenyl first
Oxysilane, ethyl propinyl phenylmethoxysilane, phenyl triethoxysilane, diphenyl diethoxy silane, triphenyl
Ethoxysilane, aminomethyl phenyl diethoxy silane, Ethylphenyldiethoxysandne, propyl phenyl diethoxy silane, second
Alkenyl phenyl diethoxy silane, acrylic phenyl diethoxy silane, ethynyl phenyl diethoxy silane, propinyl phenyl
Diethoxy silane, methyldiphenylethoxysilane, ethyl diphenyl Ethoxysilane, propyl diphenyl Ethoxysilane,
Vinyl diphenyl Ethoxysilane, acrylic diphenyl Ethoxysilane, acetenyl diphenyl Ethoxysilane, propinyl two
Phenyl ethoxy silane, 3,5-dimethylphenyl Ethoxysilane, diethyl phenyl Ethoxysilane, dipropyl phenyl ethoxy silicon
Alkane, divinyl phenyl ethoxy silane, diallyl phenyl ethoxy silane, diacetylene phenyl ethoxy silane, dipropyl
Alkynyl phenyl Ethoxysilane, Methylethyl phenyl ethoxy silane, methyl-propyl phenyl ethoxy silane, ethyl propyl phenyl
Ethoxysilane, methyl vinyl phenyl Ethoxysilane, ethyl propylene base phenyl ethoxy silane, methylacetylenyl phenyl second
At least one of oxysilane and ethyl propinyl phenyl ethoxy silane.
The flame retardant property of resin can be improved by using above-mentioned phenyl siloxane monomer in the present invention, can also improve tree
Oxidation stability, heat resistance, flame resistance, ultraviolet-resistent property and the chemical resistance of rouge.More preferably, the phenyl siloxane monomer
The mixture being made of aminomethyl phenyl dimethoxysilane and aminomethyl phenyl diethoxy silane with weight ratio 2-4:1.
The structural formula of the polymerized monomer of the cyclic siloxane monomer isWherein R5And R6Respectively
Any one in hydrogen, methyl, ethyl, propyl, vinyl, acrylic, acetenyl, propinyl and phenyl, the ring-type silicon oxygen
Polymerization degree n=3-6 of alkane monomer.The substituent group R of each polymerized monomer5And R6It may be the same or different.
Preferably, the cyclic siloxane monomer is hexamethyl cyclotrisiloxane, octamethylcy-clotetrasiloxane, decamethyl ring
Five siloxanes, ten diformazan basic rings, six siloxanes, hexaetcycletrisiloxane, octaethyl cyclotetrasiloxane, ten ethyl rings, five silicon oxygen
Alkane, ten diethyl basic rings, six siloxanes, hexaphenyl cyclotrisiloxane, octaphenylcyclotetrasiloxane, ten phenyl cyclopentasiloxanes, 12
Six siloxanes of benzyl ring, six vinyl cyclotrisiloxane, eight vinyl cyclotetrasiloxanes, ten vinyl cyclopentasiloxanes, 12
Six siloxanes of ethylene basic ring, three hydrogen trimethyl cyclotrisiloxane, trimethyl triethyl group cyclotrisiloxane, trimethyl triphenyl ring three
Siloxanes, triethyl group triphenyl cyclotrisiloxane, trimethyl trivinyl cyclotrisiloxane, three silicon oxygen of trivinyl triphen basic ring
Alkane, diethyl tetramethyl-ring trisiloxanes, dimethyl tetraethyl cyclotrisiloxane, divinyl tetramethyl-ring trisiloxanes, two
Methyl tetravinyl cyclotrisiloxane, diphenyltetramethyl cyclotrisiloxane, dimethyl tetraphenyl cyclotrisiloxane, vinyl five
Methyl cyclotrisiloxane, five vinyl cyclotrisiloxane of methyl, phenyl pentamethyl cyclotrisiloxane, five benzyl ring of methyl, three silicon oxygen
Alkane, tetrahydro tetramethyl-ring tetrasiloxane, tetramethyl tetraethyl cyclotetrasiloxane, tetramethyl tetraphenyl cyclotetrasiloxane, tetraethyl
Tetraphenyl cyclotetrasiloxane, t etram-ethyltetravinylcyclotetrasiloxane, tetravinyl tetraphenyl cyclotetrasiloxane, diethyl pregnancy
Basic ring tetrasiloxane, dimethyl Hexaethyl cyclotetrasiloxane, divinyl hexamethyl cyclotetrasiloxane, six ethylene basic ring of dimethyl
Tetrasiloxane, diphenyl hexamethyl cyclotetrasiloxane, dimethyl hexaphenyl cyclotetrasiloxane, seven methyl ring of vinyl, four silicon oxygen
In alkane, seven phenyl cyclotetrasiloxane of seven vinyl cyclotetrasiloxane of methyl, phenyl heptamethylcyclotetrasiloxane and methyl at least
It is a kind of.
The present invention can control the partial size of polymer by using above-mentioned cyclic siloxane monomer, to improve resin
Anti-flammability and impact strength.More preferably, the cyclic siloxane monomer is by trimethyl triethyl group cyclotrisiloxane, two
The mixing that six vinyl cyclotetrasiloxane of methyl and seven phenyl cyclotetrasiloxane of methyl are formed with weight ratio 2-4:0.5-1.5:1
Object.
The structural formula of the vinylsiloxane monomer are as follows:Wherein, R7, R8, R9 and R10 are respectively
Hydrogen, methyl, ethyl, propyl, vinyl, acrylic, styryl, γ-methacryloxypropyl, styryl, 2- are (right
Ethenylphenyl) ethyl, 3- (to vinylbenzoyl oxygroup) propyl, acetenyl, propinyl, methoxyl group, ethyoxyl and phenyl
In any one, and R7, R8, R9 and R10 at least one be vinyl, acrylic, styryl, γ-methacryl
Oxygroup propyl, styryl, 2- (to ethenylphenyl) ethyl or 3- (to vinylbenzoyl oxygroup) propyl, at least one
For methoxy or ethoxy.
Preferably, the vinylsiloxane monomer is vinyltrimethoxysilane, vinyltriethoxysilane, two
Vinyl dimethoxysilane, divinyl diethoxy silane, vinyl methyl dimethoxysilane, vinyl methyl diethyl
Oxysilane, vinyl ethyldimethoxysilane, vinyl ethyl diethoxy silane, vinyl dimethylamine oxygroup silicon
Alkane, vinyl propyl diethoxy silane, to vinyl phenylmethyl methoxy silane, to vinyl phenylmethyl ethyoxyl silicon
Alkane, to ethenylphenyl ethyl methoxy silane, to ethenylphenyl ethyl Ethoxysilane, styryl trimethoxy silicon
Alkane, styryl triethoxysilane, 2- (to ethenylphenyl) ethyl-methyl dimethoxysilane, 2- (to ethenylphenyl)
Ethyl-methyl diethoxy silane, 3- (to vinylbenzoyl oxygroup) hydroxypropyl methyl dimethoxysilane, 3- are (to vinyl benzene
Formyloxy) hydroxypropyl methyl diethoxy silane, acrylic trimethoxy silane, acrylic triethoxysilane, acrylic first
Base dimethoxysilane, propenylmethyl diethoxy silane, acrylic ethyldimethoxysilane, acrylic ethyl diethoxy
Base silane, acrylic propyldimethoxy-silane, acrylic propyl diethoxy silane, γ-mercaptopropyi methyl dimethoxy oxygroup
Silane, γ-methacryloxypropyl methoxyl group dimethylsilane, γ-methacryloxypropyl dimethoxy-methyl
Silane, γ-methacryloxypropyl trimethoxy silane, γ-methacryloxypropyl ethyoxyl dimethylsilane,
γ-methacryloxypropyl diethoxymethylsilane, γ-methacryloxypropyl morpholine silane,
γ-methacryloxypropyl dimethoxy-ethyl silane, γ-methacryloxypropyl ethyoxyl diethylsilane,
In γ-methacryloxypropyl diethoxy ethylsilane and γ-methacryloxypropyl
It is at least one.
The present invention can be used as coupling agent use, in organic poly- silicon by using above-mentioned vinylsiloxane monomer
The side chain of oxygen alkane or end import the ingredient of vinyl polymerized functional group, the vinyl polymerized functional group as with by being copolymerized
Monomer formed copolymerized polymer chemical bonding when grafting active site and play a role.More preferably, the vinyl silicon
Oxygen alkane monomer be by vinyl propyldimethoxy-silane, to vinyl phenylmethyl Ethoxysilane and 3- (to vinyl benzene
Formyloxy) mixture that is formed with weight ratio 2-4:1.5-2.5:1 of hydroxypropyl methyl diethoxy silane.
Preferably, in the step B, the structural formula of catalyst are as follows:Wherein, it is 1- that R ', which is carbon atom number,
10 alkyl, alkenyl, aromatic radical or carbon atom number is the naphthenic base of 3-10, cycloalkenyl.
Specifically, the catalyst is methane sulfonic acid, trifluoromethane sulfonic acid, methylol sulfonic acid, ethylsulfonic acid, trifluoroethyl
Sulfonic acid, isethionic acid, propyl sulfonic acid, hydroxypropyl sulfonic acid, 1- butyl sulfonic acid, vinyl sulfonic acid, propene sulfonic acid, metering system sulphur
Acid, ethyl propylene sulfonic acid, benzene sulfonic acid, toluenesulfonic acid, ethyl phenenyl azochlorosulfonate acid, acid dimethyl, diethylbenzene sulfonic acid and 12
At least one of alkyl benzene sulphonate.
The present invention is easy to make the particle diameter distribution of organic polysiloxane emulsion narrow by using above-mentioned catalyst, in addition, being easy
Reduction the phenomenon that resin bad order, can also improve resin in low temperature as caused by the emulsifier component of organopolysiloxane
Impact strength.More preferably, the catalyst is by methylol sulfonic acid, trifluoroethyl sulfonic acid and hydroxypropyl sulfonic acid with weight
Than the mixture of 1:0.8-1.2:0.4-0.8 composition.
In the step B, step C1 and step D2, emulsifier is by cationic surfactant, anion surface active
The mixture that agent and nonionic surfactant are formed with weight ratio 0.4-0.8:1:0.2-0.6.
Preferably, the cationic surfactant is by dialkyl dimethyl quaternary ammonium salt, benzalkonium dimethyl quaternary ammonium
The mixture that salt and monoalkyl quaternary ammonium salts are formed with weight ratio 1:1.2-1.6:1.8-2.6;The anionic surfactant is
By polyoxyethylene alkyl ether hydrogen sulfuric acid ester, alkyl diphenyl base ether disulfonate and polyoxyethylene alkyl ether ester with weight ratio 1:0.5-
1.5:1.4-2.2 the mixture of composition;The nonionic surfactant is by isomeric alcohol polyethenoxy ether, sorbitan
The mixture that aliphatic ester and polyoxyethylene hardened castor oil aliphatic ester are formed with weight ratio 1.6-2.4:1:0.8-1.2.This
The type, multiple that invention passes through strict control cationic surfactant, anionic surfactant and nonionic surfactant
Match and match, emulsifying effectiveness is good, is conducive to the emulsion dispersion of organosiloxane monomer, accelerates reaction and carries out.
In the step C2 and the step D2, cladding monomer is by α-methylstyrene, methacrylonitrile, acrylic acid 2-
Ethylhexyl, isobornyl methacrylate, fumaric acid and N- methylmaleimido are with weight ratio 1.5-2.5:1-2:0.5-
1.5:1:0.4-0.8:0.2-0.6 the mixture of composition.The present invention is coated the type of monomer by strict control, compounds and match
Than covered effect is good, and with organopolysiloxane core emulsion polymerization, the anti-flammability, heat resistance and shock resistance of resin can be improved
Performance.
In the step C2 and the step D2, initiator is by isopropyl benzene hydroperoxide, azodiisobutyronitrile and tetrem
The mixture that alkene imines is formed with weight ratio 1:0.5-1.5:1.5-2.5.The present invention passes through the type of strict control initiator, answers
Match and match, initiation effect is good, can trigger free radical polymerization and copolymerization, can improve rate of polymerization.
In the step D1, the average molecular weight of PTFE emulsion is 1,000,000-1,000 ten thousand, and solid content is in 58%-62%, cream
Liquid partial size is at 0.01-0.30 μm, viscosity 10-40*10-3Pa.S.The present invention passes through the mean molecule of strict control PTFE emulsion
Amount, solid content, emulsion particle diameter and viscosity, can improve plastic melt intensity and bending modulus, and flame-retardant anti-dropping effect makes thermoplastic materials
Reach higher flame-retardant standard.
Preferably, in the step D1, dispersing agent is inorganic dispersing agent and/or organic dispersing agent;
The inorganic dispersing agent be natural silicate, Sulfates, carbonate, Oxalates, hydroxide species and
It is at least one of oxide-based;
The natural silicate is at least one of talcum, bentonite, diatomite and kaolin;The Sulfates are
Calcium sulfate and/or barium sulfate;The carbonate is at least one of calcium carbonate, barium carbonate and magnesium carbonate;The oxalates
Class is calcium oxalate;The hydroxide species are at least one of aluminium hydroxide, magnesium hydroxide and calcium hydroxide;The oxide
Class is titanium dioxide and/or zinc oxide;
The organic dispersing agent is natural polymer subclass dispersing agent, protein-based macromolecule dispersing agent, cellulose family spread out
Biological species dispersing agent, synthesis high score subclass dispersing agent, the synthesis of class containing carboxyl macromolecule dispersing agent, the synthesis macromolecule dispersion of nitrogenous class
At least one of agent and ester-containing base class synthesis macromolecule dispersing agent;
The natural polymer subclass dispersing agent is at least one of carbohydrate starch, pectin, natural plant gum and seaweed glue;It is described
Protein-based macromolecule dispersing agent is gelatin and/or Fish protein;The cellulose derivative class dispersing agent be methylcellulose,
At least one of methylhydroxypropylcellulose, hydroxyethyl cellulose and hydroxypropyl cellulose;The synthesis high score subclass dispersion
Agent is hydroxyl class partial alcoholysis polyvinyl alcohol;The synthesis macromolecule dispersing agent of class containing carboxyl is total for phenylethylene/maleic anhydride
Polymers, vinyl acetate/copolymer-maleic anhydride and at least one of acrylic copolymer and methacrylic copolymer;
The nitrogenous class synthesis macromolecule dispersing agent is polyvinylpyrrolidone;The ester-containing base class synthesis macromolecule dispersing agent is poly-
Ethylene oxide fatty acid esters and/or sorbitan fatty acid.
For the present invention by using above-mentioned dispersing agent, dispersion effect is good, is conducive to organopolysiloxane core lotion and PTFE
The dispersion of lotion is accelerated reaction and is carried out.More preferably, the dispersing agent is by diatomite, calcium carbonate, methylhydroxypropyl
The mixture that element and sorbitan fatty acid are formed with weight ratio 1-2:0.5-1.5:1:0.8-1.2.
A kind of organic silicon fibre retardant containing PTFE and nano silica, the organic silicon fibre retardant is according to described above
Preparation method is made.
It is a kind of using anti-flaming polycarbonate made from the organic silicon fibre retardant described above containing PTFE and nano silica
Ester material, the flame-retardant polycarbonate material include the raw material of following parts by weight: 80-120 parts of polycarbonate, glass fibre 20-
40 parts, it is 0.1-1.0 parts of organic silicon fibre retardant, 4-8 parts of modifying agent, auxiliary agent 1-10 parts other;
Wherein, the modifying agent is more created by macromolecule modified nanometer calcium carbonate, hyperbranched polyester amide and 4- allyl
The mixture that the wooden phenol modified dimethyl polysiloxane is formed with weight ratio 2-6:0.1-1.0:0.5-1.5.
Flame-retardant polycarbonate material of the invention can be improved the intensity of material, pass through addition by the way that glass fibre is added
The flame retardant property of material can be improved in organic silicon fibre retardant, and by the way that modifying agent is added, the processing thermostabilization of material can be improved
Property, mechanical mechanics property and appearance.
Preferably, the preparation method of the macromolecule modified nanometer calcium carbonate includes the following steps:
(1) 15-25g nanometer calcium carbonate and 0.3-0.7g calgon dispersing agent are added into 300-500mL distilled water,
Disperse 20-28h;60-100g Polymeric quaternary ammonium salts are dissolved in 200-400mL tetrahydrofuran simultaneously, dispersion 20-28h is spare;
(2) the addition 200-400mL tetrahydrofuran into scattered nanometer calcium carbonate system, high speed dispersion 0.3-0.7h,
Then slurries are transferred in there-necked flask, polymeric quartenary ammonium salting liquid is slowly added dropwise under stirring, system constantly generates white flock
Precipitating;
(3) after completion of dropwise addition, system is warming up to 75-85 DEG C, after reacting 20-28h, then slurries is filtered, 55-65 DEG C of vacuum
Dry 24-48h, obtains macromolecule modified nanometer calcium carbonate;
Wherein, in the step (1), Polymeric quaternary ammonium salts be brominated polyphenylether stearyl dimethyl benzyl ammonium chloride,
Dimethyl diallyl ammonium chloride-acrylamide copolymer, polydimethyl diallyl ammonium chloride, chlorination -2- hydroxyl -3- (three
Methylamino) propyl polyethylene oxide cellulose ether and N, N, N- trimethyl-2- (2- methyl-1-oxo-2- acrylic oxygroup) second
At least one of ammonium chloride-acrylamide copolymer.
The present invention passes through raw material, preparation step and the technological parameter of stringent macromolecule modified nanometer calcium carbonate, height obtained
The processing heat stability and mechanical property of polycarbonate can be improved in molecular modification nanometer calcium carbonate.Preferably, the polymer
Quaternary ammonium salt is by brominated polyphenylether stearyl dimethyl benzyl ammonium chloride, chlorination -2- hydroxyl -3- (dimethylamino) propyl polycyclic
Oxidative ethane cellulose ether and N, N, N- trimethyl-2- (2- methyl-1-oxo-2- acrylic oxygroup) ethyl ammonium chloride-acryloyl
The mixture that amine copolymer object is formed with weight ratio 2-4:1.5-2.5:1.
Preferably, the synthetic method of the hyperbranched polyester amide are as follows: under nitrogen protection, successively by 0.8-1.2mol tri-
Ethanol amine, 0.8-1.2mol 1,2,4- trimellitic anhydride and 0.005-0.015mol Catalyzed by p-Toluenesulfonic Acid agent are added three mouthfuls
Round-bottomed flask is placed in heating oil bath, and stirring is gradually warming up to 210-230 DEG C, after raw material is uniformly mixed bleach,
Continue to be stirred to react 2-4h at a temperature of 210-230 DEG C, be then cooled to room temperature, obtains yellow transparent solid body i.e. hyper-branched polyester acyl
Amine.
The present invention passes through the raw material of stringent hyperbranched polyester amide, preparation step and technological parameter, hyperbranched poly obtained
Esteramides can not only improve the processing fluidity of polycarbonate, while can also improve the mechanical performance and surface smoothness of product,
And the variation of polycarbonate color will not be caused.
Preferably, the synthetic method of the 4- allyl guaiacol modified dimethyl polysiloxane are as follows: temperature is being housed
It counts, in the there-necked flask of blender, sequentially adds 230-270g dimethyl silicone polymer, 23-27g 4- allyl at room temperature and more create
The wooden phenol forms the suspension of White-opalescent after stirring;Add the chlorine platinum that 0.5-1.0mL platinum mass fraction is 1.5-2.5%
The octanol solution of acid;Continue to stir, is warming up to 90-100 DEG C under logical nitrogen, reacts 2-4h.
Raw material, preparation step and the technique that the present invention passes through stringent 4- allyl guaiacol modified dimethyl polysiloxane
The tensile strength of polycarbonate, bending can be improved in parameter, 4- allyl guaiacol modified dimethyl polysiloxane obtained
Intensity, impact strength and elongation at break.
Preferably, the melt index of the polycarbonate is bisphenol A-type poly- carbonic acid of the melt index in 10-50g/10min
At least one of ester, polyester-type polycarbonate and hexamethylene bisphenol A polycarbonate.
The present invention is by using above-mentioned polycarbonate, and the melt index of strict control polycarbonate is that melt index exists
10-50g/10min, so that polycarbonate has high-intensitive and coefficient of elasticity, high impact, use temperature range wide, forming
Shrinking percentage is low, and dimensional stability is good, and fatigue durability and weatherability are good, and electrical characteristic is excellent, colorless and odorless, safety and environmental protection.More
Preferably, the polycarbonate is by bisphenol A polycarbonate, polyester-type polycarbonate and hexamethylene bisphenol A polycarbonate
The mixture formed with weight ratio 1-2:0.8-1.2:1.
The glass fibre be fibre diameter 5-15 μm, fibre length 1-10mm alkali-free short glass fiber.
The present invention by using fibre diameter 5-15 μm, fibre length 1-10mm alkali-free short glass fiber,
Good insulating, heat resistance is strong, and corrosion resistance is good, high mechanical strength, and the intensity of plastics can be improved.
Other described auxiliary agents are at least one of antioxidant, UV resistant agent, lubricant, smoke suppressant and Vitrified powder.This
The antioxygenic property, anti-ultraviolet property, processability of makrolon material can be improved by using other above-mentioned auxiliary agents in invention
Can, flame-retardant smoke inhibition effect is good.More preferably, other described auxiliary agents are by antioxidant, UV resistant agent, lubricant, smoke suppressant
The mixture formed with Vitrified powder with weight ratio 0.4-0.8:0.6-1.0:1:0.5-1.5:0.8-1.2.
Preferably, the antioxidant is by β-(3,5- di-tert-butyl-hydroxy phenyl) propionic acid n-octadecyl alcohol ester, three
The mixing that [2.4- di-tert-butyl-phenyl] phosphite ester and the double lauryls of thio-2 acid are formed with weight ratio 1-2:0.8-1.2:1
Object.The present invention passes through type, compounding and the weight proportion of strict control antioxidant, can delay or inhibit material oxidation process
It carries out, to prevent the aging of material and prolong its service life.
Preferably, the UV resistant agent is by 2- (2 '-hydroxyls -5 '-aminomethyl phenyl) benzotriazole, 2- hydroxyl -4-
The mixture that methoxy benzophenone and hexamethylphosphoramide are formed with weight ratio 0.5-1.5:1.4-2.2:1.The present invention is logical
The type, compounding and weight proportion for crossing strict control ultraviolet absorbing agent, can absorb ultraviolet light strongly, imitate with excellent collaboration
It answers.
Preferably, the lubricant is by oxidized polyethylene wax, glycerin monostearate and stearic amide with weight ratio
1-2:0.4-0.8:1 the mixture of composition.The present invention passes through type, compounding and the proportion of strict control lubricant, can make material
Material improves the mobility of material and the release property of product in process, can reduce difficulty of processing, saves energy consumption.
Preferably, the smoke suppressant is by ferrocene, antimony oxide and ammonium octamolybdate with weight ratio 0.5-1.5:1.5-
2.5:1 the mixture of composition.For the present invention by type, compounding and the proportion of strict control smoke suppressant, smoke suppressing effect is good, can be with
Reduce toxic gas and smog that thermoplastic polyurethane is generated in burning.
Preferably, the Vitrified powder is by attapulgite, zinc borate, silicate glass powder with weight ratio 2-4:0.5-1.5:
The mixture of 1 composition.The present invention by type, compounding and the proportion of strict control Vitrified powder, it is moldable can be at 600-1000 DEG C
Fine and close ceramic product is formed in range, the ceramic product of formation has good elevated temperature strength and heat resistanceheat resistant stream impact energy
Power also has good mechanical property at normal temperature.
The beneficial effects of the present invention are: preparation methods of the invention by by organic matter and Nano-meter SiO_22Hydridization, with
Cladding monomer is added after PTFE mixing to be coated, the organic silicon fibre retardant containing PTFE and nano silica, technique letter is made
It is single, it is at low cost.
The resistance to thermal decomposition temperature of organic silicon fibre retardant had not only can be improved in organic silicon fibre retardant of the invention, but also had fire retardant
Anti-dripping effects also improves the flame retardant property of organic silicon fibre retardant.
Specific embodiment
For the ease of the understanding of those skilled in the art, below with reference to embodiment, the present invention is further illustrated, real
The content that the mode of applying refers to not is limitation of the invention.
Embodiment 1
A kind of preparation method of the organic silicon fibre retardant containing PTFE and nano silica, includes the following steps:
A, Nano-meter SiO_22Surface it is modified:
A1, configuration ethanol/water solution, are added Nano-meter SiO_22Particle, the high speed shear under the revolving speed of 3000rpm;Wherein, second
The volume ratio of alcohol and water is 3:1, Nano-meter SiO_22The dosage of particle is the 0.1% of ethanol/water solution quality;
A2, silane coupling agent is added, adding oxalic acid solution makes the pH value of reaction system 3, after reacting 1.5h, filter,
Washing, the Nano-meter SiO_2 modified up to surface after dry2Particle;Wherein, the dosage of silane coupling agent is Nano-meter SiO_22Mass particle
1%;
B, the synthesis of organopolysiloxane core lotion:
Organosiloxane monomer is uniformly mixed, is added in the aqueous solution dissolved with catalyst and emulsifier, at 30 DEG C
At a temperature of react 10h, obtain organopolysiloxane core lotion;Wherein, the gross mass of organosiloxane monomer is water quality
40%, the dosage of catalyst is the 1% of organosiloxane monomer mass, and the dosage of emulsifier is organosiloxane monomer mass
1%;
C, hydridization organic matter/Nano-meter SiO_22The preparation of lotion:
C1, it takes emulsifier soluble in water, the Nano-meter SiO_2 modified by surface is added2Particle is dispersed using ultrasonic wave
10min obtains dispersion liquid;Wherein, the dosage of emulsifier is the 1% of water quality, by the modified Nano-meter SiO_2 in surface2Particle
Dosage is the 0.1% of water quality;
C2, then dispersion liquid is added in organopolysiloxane core lotion, cladding monomer and initiator is added, caused poly-
Reaction is closed, hydridization organic matter/Nano-meter SiO_2 is obtained2Lotion;Wherein, the dosage of dispersion liquid is organopolysiloxane core quality of the emulsion
10%, the dosage for coating monomer is the 30% of organopolysiloxane core quality of the emulsion, and the dosage of initiator is organic poly- silicon oxygen
The 0.1% of alkane core quality of the emulsion;
D, contain PTFE and Nano-meter SiO_22Organic silicon fibre retardant preparation:
D1, by hydridization organic matter/Nano-meter SiO_22Lotion, PTFE emulsion, dispersing agent and distilled water are added to reaction kettle together
In, the high shear agitation 25min under 1000rpm revolving speed;Wherein, the dosage of PTFE emulsion is hydridization organic matter/Nano-meter SiO_22
The 10% of quality of the emulsion, the dosage of dispersing agent are hydridization organic matter/Nano-meter SiO_22The 1% of quality of the emulsion;
D2, cladding monomer is added, adds emulsifier and initiator, reacts 10h at 50 °C;Wherein, cladding is single
The dosage of body is hydridization organic matter/Nano-meter SiO_22The 30% of quality of the emulsion, the dosage of emulsifier are hydridization organic matter/Nano-meter SiO_22
The 1% of quality of the emulsion, the dosage of initiator are hydridization organic matter/Nano-meter SiO_22The 0.1% of quality of the emulsion;
D3, reaction product washed, is centrifuged, drying drying, the having containing PTFE and nano silica is made
Machine silicon fire retardant;
Wherein, in the step A2, silane coupling agent is by 3- aminopropyl trimethoxysilane, three (beta-methoxy of vinyl
Base oxethyl) mixture that is formed with weight ratio 2:1.5:1 of silane and γ-methacryloxypropyl trimethoxy silane.
In the step B, organosiloxane monomer is by phenyl siloxane monomer, cyclic siloxane monomer and vinyl silicon
The mixture that oxygen alkane monomer is formed with weight ratio 4:2:0.1;
The phenyl siloxane monomer is phenyltrimethoxysila,e, dimethoxydiphenylsilane, triphenylmethoxy
Silane, aminomethyl phenyl dimethoxysilane, ethylphenyl dimethoxysilane, propyl phenyidimethoxysilane, vinyl benzene
Base dimethoxysilane, acrylic phenyidimethoxysilane, ethynyl phenyl dimethoxysilane, propinyl phenyl dimethoxy
Base silane, methyldiphenyl methoxylsilane, ethyl diphenyl methoxy silane or propyl diphenylmethyl oxysilane.
The cyclic siloxane monomer is hexamethyl cyclotrisiloxane, octamethylcy-clotetrasiloxane, five silicon oxygen of decamethyl ring
Alkane, ten diformazan basic rings, six siloxanes, hexaetcycletrisiloxane, octaethyl cyclotetrasiloxane, ten ethyl cyclopentasiloxanes, 12
Six siloxanes of ethyl ring, hexaphenyl cyclotrisiloxane, octaphenylcyclotetrasiloxane, ten phenyl cyclopentasiloxanes, ten hexichol basic rings
Six siloxanes, six vinyl cyclotrisiloxane or eight vinyl cyclotetrasiloxanes.
The vinylsiloxane monomer is vinyltrimethoxysilane, vinyltriethoxysilane, divinyl
Dimethoxysilane, divinyl diethoxy silane, vinyl methyl dimethoxysilane, vinyl methyl diethoxy silicon
Alkane, vinyl ethyldimethoxysilane, vinyl ethyl diethoxy silane, vinyl propyldimethoxy-silane, ethylene
Base propyl diethoxy silane or to vinyl phenylmethyl methoxy silane.
In the step B, catalyst is methane sulfonic acid, trifluoromethane sulfonic acid, methylol sulfonic acid or ethylsulfonic acid;
In the step B, step C1 and step D2, emulsifier is by cationic surfactant, anion surface active
The mixture that agent and nonionic surfactant are formed with weight ratio 0.4:1:0.2;
In the step C2 and the step D2, cladding monomer is by α-methylstyrene, methacrylonitrile, acrylic acid 2-
Ethylhexyl, isobornyl methacrylate, fumaric acid and N- methylmaleimido are with weight ratio 1.5:1:0.5:1:0.4:
The mixture of 0.2 composition;
In the step C2 and the step D2, initiator is by isopropyl benzene hydroperoxide, azodiisobutyronitrile and tetrem
The mixture that alkene imines is formed with weight ratio 1:0.5:1.5;
In the step D1, the average molecular weight of PTFE emulsion is 1,000,000, and solid content is 58%, and emulsion particle diameter is in 0.01 μ
M, viscosity 10*10-3Pa.S。
In the step D1, dispersing agent is inorganic dispersing agent;
The inorganic dispersing agent is natural silicate, Sulfates, carbonate or Oxalates;
The natural silicate is talcum, bentonite, diatomite or kaolin;The Sulfates are calcium sulfate or sulfuric acid
Barium;The carbonate is calcium carbonate, barium carbonate or magnesium carbonate;The Oxalates are calcium oxalate.
A kind of organic silicon fibre retardant containing PTFE and nano silica, the organic silicon fibre retardant is according to described above
Preparation method is made.
It is a kind of using anti-flaming polycarbonate made from the organic silicon fibre retardant described above containing PTFE and nano silica
Ester material, the flame-retardant polycarbonate material include the raw material of following parts by weight: 80 parts of polycarbonate, has 20 parts of glass fibre
0.1 part of machine silicon fire retardant, 4 parts of modifying agent, 1 part of other auxiliary agents;
Wherein, the modifying agent is more created by macromolecule modified nanometer calcium carbonate, hyperbranched polyester amide and 4- allyl
The mixture that the wooden phenol modified dimethyl polysiloxane is formed with weight ratio 2:0.1:0.5.
The preparation method of the macromolecule modified nanometer calcium carbonate includes the following steps:
(1) 15g nanometer calcium carbonate and 0.3g calgon dispersing agent are added into 300mL distilled water, disperses 20h;Together
When 60g Polymeric quaternary ammonium salts are dissolved in 200mL tetrahydrofuran, dispersion 20h it is spare;
(2) 200mL tetrahydrofuran, high speed dispersion 0.3h, then slurry are added into scattered nanometer calcium carbonate system
Liquid is transferred in there-necked flask, and polymeric quartenary ammonium salting liquid is slowly added dropwise under stirring, and system constantly generates white flock precipitate;
(3) after completion of dropwise addition, system is warming up to 75 DEG C, after reacting 20h, then slurries is filtered, 55 DEG C of vacuum drying for 24 hours,
Obtain macromolecule modified nanometer calcium carbonate;
Wherein, in the step (1), Polymeric quaternary ammonium salts are brominated polyphenylether stearyl dimethyl benzyl ammonium chloride.
The synthetic method of the hyperbranched polyester amide are as follows: under nitrogen protection, successively by 0.8mol triethanolamine,
0.8mol1,2,4- trimellitic anhydride and 0.005mol Catalyzed by p-Toluenesulfonic Acid agent are added three neck round bottom flask and are placed in heating
In oil bath, stirring is gradually warming up to 210 DEG C, after raw material is uniformly mixed bleach, continues to be stirred to react at a temperature of 210 DEG C
2h is then cooled to room temperature, and obtains yellow transparent solid body i.e. hyperbranched polyester amide.
The synthetic method of the 4- allyl guaiacol modified dimethyl polysiloxane are as follows: equipped with thermometer, stirring
In the there-necked flask of device, 230g dimethyl silicone polymer, 23g 4- allyl guaiacol are sequentially added at room temperature, is formed after stirring
The suspension of White-opalescent;Add the octanol solution for the chloroplatinic acid that 0.5mL platinum mass fraction is 1.5%;Continue to stir, lead to
It is warming up to 90 DEG C under nitrogen, reacts 2h.
The melt index of the polycarbonate is bisphenol A polycarbonate of the melt index in 10g/10min;The glass
Fiber be fibre diameter 5 μm, fibre length 1mm alkali-free short glass fiber;Other described auxiliary agents are antioxidant.
Embodiment 2
A kind of preparation method of the organic silicon fibre retardant containing PTFE and nano silica, includes the following steps:
A, Nano-meter SiO_22Surface it is modified:
A1, configuration ethanol/water solution, are added Nano-meter SiO_22Particle, the high speed shear under the revolving speed of 3200rpm;Wherein, second
The volume ratio of alcohol and water is 5:1, Nano-meter SiO_22The dosage of particle is the 1% of ethanol/water solution quality;
A2, silane coupling agent is added, adding oxalic acid solution makes the pH value of reaction system 3.2, after reacting 1.8h, takes out
Filter, washing, the Nano-meter SiO_2 modified up to surface after dry2Particle;Wherein, the dosage of silane coupling agent is Nano-meter SiO_22Particle matter
The 3% of amount;
B, the synthesis of organopolysiloxane core lotion:
Organosiloxane monomer is uniformly mixed, is added in the aqueous solution dissolved with catalyst and emulsifier, at 40 DEG C
At a temperature of react 9h, obtain organopolysiloxane core lotion;Wherein, the gross mass of organosiloxane monomer is water quality
45%, the dosage of catalyst is the 2% of organosiloxane monomer mass, and the dosage of emulsifier is organosiloxane monomer mass
5%;
C, hydridization organic matter/Nano-meter SiO_22The preparation of lotion:
C1, it takes emulsifier soluble in water, the Nano-meter SiO_2 modified by surface is added2Particle is dispersed using ultrasonic wave
15min obtains dispersion liquid;Wherein, the dosage of emulsifier is the 1%~20% of water quality, by the modified Nano-meter SiO_2 in surface2
The dosage of particle is the 1% of water quality;
C2, then dispersion liquid is added in organopolysiloxane core lotion, cladding monomer and initiator is added, caused poly-
Reaction is closed, hydridization organic matter/Nano-meter SiO_2 is obtained2Lotion;Wherein, the dosage of dispersion liquid is organopolysiloxane core quality of the emulsion
20%, the dosage for coating monomer is the 40% of organopolysiloxane core quality of the emulsion, and the dosage of initiator is organic poly- silicon oxygen
The 0.3% of alkane core quality of the emulsion;
D, contain PTFE and Nano-meter SiO_22Organic silicon fibre retardant preparation:
D1, by hydridization organic matter/Nano-meter SiO_22Lotion, PTFE emulsion, dispersing agent and distilled water are added to reaction kettle together
In, the high shear agitation 20min under 1200rpm revolving speed;Wherein, the dosage of PTFE emulsion is hydridization organic matter/Nano-meter SiO_22
The 20% of quality of the emulsion, the dosage of dispersing agent are hydridization organic matter/Nano-meter SiO_22The 2% of quality of the emulsion;
D2, cladding monomer is added, adds emulsifier and initiator, reacts 9h at a temperature of 60 DEG C;Wherein, monomer is coated
Dosage be hydridization organic matter/Nano-meter SiO_22The 40% of quality of the emulsion, the dosage of emulsifier are hydridization organic matter/Nano-meter SiO_22Cream
The 5% of liquid quality, the dosage of initiator are hydridization organic matter/Nano-meter SiO_22The 0.3% of quality of the emulsion;
D3, reaction product washed, is centrifuged, drying drying, the having containing PTFE and nano silica is made
Machine silicon fire retardant;
Wherein, in the step A2, silane coupling agent is by 3- aminopropyl trimethoxysilane, three (beta-methoxy of vinyl
Base oxethyl) mixing that is formed with weight ratio 2.5:1.8:1 of silane and γ-methacryloxypropyl trimethoxy silane
Object.
In the step B, organosiloxane monomer is by phenyl siloxane monomer, cyclic siloxane monomer and vinyl silicon
The mixture that oxygen alkane monomer is formed with weight ratio 5:3:0.3;
The phenyl siloxane monomer is vinyl diphenyl methoxy silane, acrylic diphenylmethyl oxysilane, second
Alkynyl diphenylmethyl oxysilane, propinyl diphenylmethyl oxysilane, dimethyl benzene methoxylsilane, diethyl phenyl first
Oxysilane, dipropyl phenylmethoxysilane, divinyl phenylmethoxysilane, diallyl phenylmethoxysilane,
Diacetylene phenylmethoxysilane, dipropyl alkynyl phenyl methoxy silane, Methylethyl phenylmethoxysilane, methyl-propyl
Phenylmethoxysilane, ethyl propyl phenylmethoxysilane or methyl vinyl phenyl methoxy silane.
The cyclic siloxane monomer is ten vinyl cyclopentasiloxanes, ten divinyl basic rings, six siloxanes, three hydrogen front threes
Basic ring trisiloxanes, trimethyl triethyl group cyclotrisiloxane, trimethyl triphenyl cyclotrisiloxane, three silicon of triethyl group triphen basic ring
Oxygen alkane, trimethyl trivinyl cyclotrisiloxane, trivinyl triphenyl cyclotrisiloxane, diethyl tetramethyl-ring trisiloxanes
Or dimethyl tetraethyl cyclotrisiloxane.
The vinylsiloxane monomer is to vinyl phenylmethyl Ethoxysilane, to ethenylphenyl ethyl methoxy
Base silane, to ethenylphenyl ethyl Ethoxysilane, styryltrimethoxysilane, styryl triethoxysilane,
2- (to ethenylphenyl) ethyl-methyl dimethoxysilane or 2- (to ethenylphenyl) ethyl-methyl diethoxy silane.
In the step B, catalyst is trifluoroethyl sulfonic acid, isethionic acid, propyl sulfonic acid, hydroxypropyl sulfonic acid or 1- fourth
Base sulfonic acid;
In the step B, step C1 and step D2, emulsifier is by cationic surfactant, anion surface active
The mixture that agent and nonionic surfactant are formed with weight ratio 0.5:1:0.3;
In the step C2 and the step D2, cladding monomer is by α-methylstyrene, methacrylonitrile, acrylic acid 2-
Ethylhexyl, isobornyl methacrylate, fumaric acid and N- methylmaleimido are with weight ratio 1.8:1.2:08:1:0.6:
The mixture of 0.3 composition;
In the step C2 and the step D2, initiator is by isopropyl benzene hydroperoxide, azodiisobutyronitrile and tetrem
The mixture that alkene imines is formed with weight ratio 1:0.8:1.8;
In the step D1, the average molecular weight of PTFE emulsion is 3,000,000, and solid content is 59%, and emulsion particle diameter is in 0.05 μ
M, viscosity 20*10-3Pa.S。
In the step D1, dispersing agent is inorganic dispersing agent;
The inorganic dispersing agent is hydroxide species or oxide-based;
The hydroxide species are aluminium hydroxide, magnesium hydroxide or calcium hydroxide;It is described it is oxide-based for titanium dioxide or
Zinc oxide.
A kind of organic silicon fibre retardant containing PTFE and nano silica, the organic silicon fibre retardant is according to described above
Preparation method is made.
It is a kind of using anti-flaming polycarbonate made from the organic silicon fibre retardant described above containing PTFE and nano silica
Ester material, the flame-retardant polycarbonate material include the raw material of following parts by weight: 90 parts of polycarbonate, has 25 parts of glass fibre
0.3 part of machine silicon fire retardant, 5 parts of modifying agent, 3 parts of other auxiliary agents;
Wherein, the modifying agent is more created by macromolecule modified nanometer calcium carbonate, hyperbranched polyester amide and 4- allyl
The mixture that the wooden phenol modified dimethyl polysiloxane is formed with weight ratio 3:0.3:0.8.
The preparation method of the macromolecule modified nanometer calcium carbonate includes the following steps:
(1) 18g nanometer calcium carbonate and 0.4g calgon dispersing agent are added into 350mL distilled water, disperses 22h;Together
When 70g Polymeric quaternary ammonium salts are dissolved in 250mL tetrahydrofuran, dispersion 22h it is spare;
(2) 250mL tetrahydrofuran, high speed dispersion 0.4h, then slurry are added into scattered nanometer calcium carbonate system
Liquid is transferred in there-necked flask, and polymeric quartenary ammonium salting liquid is slowly added dropwise under stirring, and system constantly generates white flock precipitate;
(3) after completion of dropwise addition, system is warming up to 78 DEG C, after reacting 22h, then slurries is filtered, 58 DEG C of vacuum drying 30h,
Obtain macromolecule modified nanometer calcium carbonate;
Wherein, in the step (1), Polymeric quaternary ammonium salts are dimethyl diallyl ammonium chloride-acrylamide copolymer.
The synthetic method of the hyperbranched polyester amide are as follows: under nitrogen protection, successively by 0.9mol triethanolamine,
0.9mol1,2,4- trimellitic anhydride and 0.008mol Catalyzed by p-Toluenesulfonic Acid agent are added three neck round bottom flask and are placed in heating
In oil bath, stirring is gradually warming up to 215 DEG C, after raw material is uniformly mixed bleach, continues to be stirred to react at a temperature of 215 DEG C
2.5h is then cooled to room temperature, and obtains yellow transparent solid body i.e. hyperbranched polyester amide.
The synthetic method of the 4- allyl guaiacol modified dimethyl polysiloxane are as follows: equipped with thermometer, stirring
In the there-necked flask of device, 240g dimethyl silicone polymer, 24g 4- allyl guaiacol are sequentially added at room temperature, is formed after stirring
The suspension of White-opalescent;Add the octanol solution for the chloroplatinic acid that 0.6mL platinum mass fraction is 1.8%;Continue to stir, lead to
It is warming up to 92 DEG C under nitrogen, reacts 2.5h.
The melt index of the polycarbonate is polyester-type polycarbonate of the melt index in 20g/10min;The glass
Fiber be fibre diameter 8 μm, fibre length 3mm alkali-free short glass fiber;Other described auxiliary agents are UV resistant agent.
Embodiment 3
A kind of preparation method of the organic silicon fibre retardant containing PTFE and nano silica, includes the following steps:
A, Nano-meter SiO_22Surface it is modified:
A1, configuration ethanol/water solution, are added Nano-meter SiO_22Particle, the high speed shear under the revolving speed of 3500rpm;Wherein, second
The volume ratio of alcohol and water is 7:1, Nano-meter SiO_22The dosage of particle is the 5% of ethanol/water solution quality;
A2, silane coupling agent is added, adding oxalic acid solution makes the pH value of reaction system 3.5, after reacting 2h, filter,
Washing, the Nano-meter SiO_2 modified up to surface after dry2Particle;Wherein, the dosage of silane coupling agent is Nano-meter SiO_22Mass particle
5%;
B, the synthesis of organopolysiloxane core lotion:
Organosiloxane monomer is uniformly mixed, is added in the aqueous solution dissolved with catalyst and emulsifier, at 50 DEG C
At a temperature of react 8h, obtain organopolysiloxane core lotion;Wherein, the gross mass of organosiloxane monomer is water quality
50%, the dosage of catalyst is the 3% of organosiloxane monomer mass, and the dosage of emulsifier is organosiloxane monomer mass
10%;
C, hydridization organic matter/Nano-meter SiO_22The preparation of lotion:
C1, it takes emulsifier soluble in water, the Nano-meter SiO_2 modified by surface is added2Particle is dispersed using ultrasonic wave
20min obtains dispersion liquid;Wherein, the dosage of emulsifier is the 10% of water quality, by the modified Nano-meter SiO_2 in surface2Particle
Dosage is the 5% of water quality;
C2, then dispersion liquid is added in organopolysiloxane core lotion, cladding monomer and initiator is added, caused poly-
Reaction is closed, hydridization organic matter/Nano-meter SiO_2 is obtained2Lotion;Wherein, the dosage of dispersion liquid is organopolysiloxane core quality of the emulsion
30%, the dosage for coating monomer is the 50% of organopolysiloxane core quality of the emulsion, and the dosage of initiator is organic poly- silicon oxygen
The 0.5% of alkane core quality of the emulsion;
D, contain PTFE and Nano-meter SiO_22Organic silicon fibre retardant preparation:
D1, by hydridization organic matter/Nano-meter SiO_22Lotion, PTFE emulsion, dispersing agent and distilled water are added to reaction kettle together
In, the high shear agitation 15min under 1500rpm revolving speed;Wherein, the dosage of PTFE emulsion is hydridization organic matter/Nano-meter SiO_22
The 30% of quality of the emulsion, the dosage of dispersing agent are hydridization organic matter/Nano-meter SiO_22The 3% of quality of the emulsion;
D2, cladding monomer is added, adds emulsifier and initiator, reacts 8h at a temperature of 65 DEG C;Wherein, monomer is coated
Dosage be hydridization organic matter/Nano-meter SiO_22The 50% of quality of the emulsion, the dosage of emulsifier are hydridization organic matter/Nano-meter SiO_22Cream
The 10% of liquid quality, the dosage of initiator are hydridization organic matter/Nano-meter SiO_22The 0.5% of quality of the emulsion;
D3, reaction product washed, is centrifuged, drying drying, the having containing PTFE and nano silica is made
Machine silicon fire retardant;
Wherein, in the step A2, silane coupling agent is by 3- aminopropyl trimethoxysilane, three (beta-methoxy of vinyl
Base oxethyl) mixture that is formed with weight ratio 3:2:1 of silane and γ-methacryloxypropyl trimethoxy silane.
In the step B, organosiloxane monomer is by phenyl siloxane monomer, cyclic siloxane monomer and vinyl silicon
The mixture that oxygen alkane monomer is formed with weight ratio 6:3:0.5;
The phenyl siloxane monomer is ethyl propylene base phenylmethoxysilane, methylacetylenyl Phenylmethoxy silicon
Alkane, ethyl propinyl phenylmethoxysilane, phenyl triethoxysilane, diphenyl diethoxy silane, triphen base oxethyl
Silane, aminomethyl phenyl diethoxy silane, Ethylphenyldiethoxysandne, propyl phenyl diethoxy silane, vinyl benzene
Base diethoxy silane or acrylic phenyl diethoxy silane.
The cyclic siloxane monomer is divinyl tetramethyl-ring trisiloxanes, three silicon oxygen of dimethyl tetravinyl ring
Alkane, diphenyltetramethyl cyclotrisiloxane, dimethyl tetraphenyl cyclotrisiloxane, vinyl pentamethyl cyclotrisiloxane, methyl
Five benzyl ring trisiloxanes of five vinyl cyclotrisiloxane, phenyl pentamethyl cyclotrisiloxane or methyl.
The vinylsiloxane monomer is 3- (to vinylbenzoyl oxygroup) hydroxypropyl methyl dimethoxysilane, 3-
(to vinylbenzoyl oxygroup) hydroxypropyl methyl diethoxy silane, acrylic trimethoxy silane, propylene ethyl triethoxy silicane
Alkane, propenylmethyl dimethoxysilane, propenylmethyl diethoxy silane, acrylic ethyldimethoxysilane, propylene
Base ethyl diethoxy silane, acrylic propyldimethoxy-silane or acrylic propyl diethoxy silane.
In the step B, catalyst is vinyl sulfonic acid, propene sulfonic acid, methacrylic sulfonic acid, ethyl propylene sulfonic acid or benzene
Sulfonic acid;
In the step B, step C1 and step D2, emulsifier is by cationic surfactant, anion surface active
The mixture that agent and nonionic surfactant are formed with weight ratio 0.6:1:0.4;
In the step C2 and the step D2, cladding monomer is by α-methylstyrene, methacrylonitrile, acrylic acid 2-
Ethylhexyl, isobornyl methacrylate, fumaric acid and N- methylmaleimido are with weight ratio 2:1.5:1:1:0.6:0.4
The mixture of composition;
In the step C2 and the step D2, initiator is by isopropyl benzene hydroperoxide, azodiisobutyronitrile and tetrem
The mixture that alkene imines is formed with weight ratio 1:1:2;
In the step D1, the average molecular weight of PTFE emulsion is 5,000,000, and solid content is 60%, and emulsion particle diameter is in 0.15 μ
M, viscosity 25*10-3Pa.S。
In the step D1, dispersing agent is organic dispersing agent;
The organic dispersing agent is that natural polymer subclass dispersing agent, protein-based macromolecule dispersing agent or cellulose family spread out
Biological species dispersing agent;
The natural polymer subclass dispersing agent is carbohydrate starch, pectin, natural plant gum or seaweed glue;The protein-based high score
Sub- dispersing agent is gelatin or Fish protein;The cellulose derivative class dispersing agent is methylcellulose, methylhydroxypropyl
Element, hydroxyethyl cellulose or hydroxypropyl cellulose.
A kind of organic silicon fibre retardant containing PTFE and nano silica, the organic silicon fibre retardant is according to described above
Preparation method is made.
It is a kind of using anti-flaming polycarbonate made from the organic silicon fibre retardant described above containing PTFE and nano silica
Ester material, the flame-retardant polycarbonate material include the raw material of following parts by weight: 100 parts of polycarbonate, has 30 parts of glass fibre
0.5 part of machine silicon fire retardant, 6 parts of modifying agent, 5 parts of other auxiliary agents;
Wherein, the modifying agent is more created by macromolecule modified nanometer calcium carbonate, hyperbranched polyester amide and 4- allyl
The mixture that the wooden phenol modified dimethyl polysiloxane is formed with weight ratio 4:0.5:1.
The preparation method of the macromolecule modified nanometer calcium carbonate includes the following steps:
(1) 20g nanometer calcium carbonate and 0.5g calgon dispersing agent are added into 400mL distilled water, dispersion is for 24 hours;Together
When 80g Polymeric quaternary ammonium salts are dissolved in 300mL tetrahydrofuran, disperse it is spare for 24 hours;
(2) 300mL tetrahydrofuran, high speed dispersion 0.5h, then slurry are added into scattered nanometer calcium carbonate system
Liquid is transferred in there-necked flask, and polymeric quartenary ammonium salting liquid is slowly added dropwise under stirring, and system constantly generates white flock precipitate;
(3) after completion of dropwise addition, system is warming up to 80 DEG C, after reaction for 24 hours, then slurries is filtered, 60 DEG C of vacuum drying 36h,
Obtain macromolecule modified nanometer calcium carbonate;
Wherein, in the step (1), Polymeric quaternary ammonium salts are polydimethyl diallyl ammonium chloride.
The synthetic method of the hyperbranched polyester amide are as follows: under nitrogen protection, successively by 1mol triethanolamine, 1mol
1,2,4- trimellitic anhydride and 0.01mol Catalyzed by p-Toluenesulfonic Acid agent are added three neck round bottom flask and are placed in heating oil bath,
Stirring, is gradually warming up to 220 DEG C, after raw material is uniformly mixed bleach, continues to be stirred to react 3h at a temperature of 220 DEG C, then
It is cooled to room temperature, obtains yellow transparent solid body i.e. hyperbranched polyester amide.
The synthetic method of the 4- allyl guaiacol modified dimethyl polysiloxane are as follows: equipped with thermometer, stirring
In the there-necked flask of device, 250g dimethyl silicone polymer, 25g 4- allyl guaiacol are sequentially added at room temperature, is formed after stirring
The suspension of White-opalescent;Add the octanol solution for the chloroplatinic acid that 0.8mL platinum mass fraction is 2%;Continue to stir, leads to nitrogen
It is warming up to 95 DEG C under gas, reacts 3h.
The melt index of the polycarbonate is hexamethylene bisphenol A polycarbonate of the melt index in 30g/10min;Institute
State glass fibre be fibre diameter 10 μm, fibre length 5mm alkali-free short glass fiber;Other described auxiliary agents are lubrication
Agent.
Embodiment 4
A kind of preparation method of the organic silicon fibre retardant containing PTFE and nano silica, includes the following steps:
A, Nano-meter SiO_22Surface it is modified:
A1, configuration ethanol/water solution, are added Nano-meter SiO_22Particle, the high speed shear under the revolving speed of 3800rpm;Wherein, second
The volume ratio of alcohol and water is 9:1, Nano-meter SiO_22The dosage of particle is the 8% of ethanol/water solution quality;
A2, silane coupling agent is added, adding oxalic acid solution makes the pH value of reaction system 3.8, after reacting 2.2h, takes out
Filter, washing, the Nano-meter SiO_2 modified up to surface after dry2Particle;Wherein, the dosage of silane coupling agent is Nano-meter SiO_22Particle matter
The 8% of amount;
B, the synthesis of organopolysiloxane core lotion:
Organosiloxane monomer is uniformly mixed, is added in the aqueous solution dissolved with catalyst and emulsifier, at 70 DEG C
At a temperature of react 6h, obtain organopolysiloxane core lotion;Wherein, the gross mass of organosiloxane monomer is water quality
55%, the dosage of catalyst is the 4% of organosiloxane monomer mass, and the dosage of emulsifier is organosiloxane monomer mass
15%;
C, hydridization organic matter/Nano-meter SiO_22The preparation of lotion:
C1, it takes emulsifier soluble in water, the Nano-meter SiO_2 modified by surface is added2Particle is dispersed using ultrasonic wave
25min obtains dispersion liquid;Wherein, the dosage of emulsifier is the 15% of water quality, by the modified Nano-meter SiO_2 in surface2Particle
Dosage is the 8% of water quality;
C2, then dispersion liquid is added in organopolysiloxane core lotion, cladding monomer and initiator is added, caused poly-
Reaction is closed, hydridization organic matter/Nano-meter SiO_2 is obtained2Lotion;Wherein, the dosage of dispersion liquid is organopolysiloxane core quality of the emulsion
40%, the dosage for coating monomer is organopolysiloxane core quality of the emulsion 60%, and the dosage of initiator is organopolysiloxane
The 0.6% of core quality of the emulsion;
D, contain PTFE and Nano-meter SiO_22Organic silicon fibre retardant preparation:
D1, by hydridization organic matter/Nano-meter SiO_22Lotion, PTFE emulsion, dispersing agent and distilled water are added to reaction kettle together
In, the high shear agitation 10min under 1800rpm revolving speed;Wherein, the dosage of PTFE emulsion is hydridization organic matter/Nano-meter SiO_22
The 40% of quality of the emulsion, the dosage of dispersing agent are hydridization organic matter/Nano-meter SiO_22The 4% of quality of the emulsion;
D2, cladding monomer is added, adds emulsifier and initiator, reacts 6h at a temperature of 70 DEG C;Wherein, monomer is coated
Dosage be hydridization organic matter/Nano-meter SiO_22The 60% of quality of the emulsion, the dosage of emulsifier are hydridization organic matter/Nano-meter SiO_22Cream
The 15% of liquid quality, the dosage of initiator are hydridization organic matter/Nano-meter SiO_22The 0.6% of quality of the emulsion;
D3, reaction product washed, is centrifuged, drying drying, the having containing PTFE and nano silica is made
Machine silicon fire retardant;
Wherein, in the step A2, silane coupling agent is by 3- aminopropyl trimethoxysilane, three (beta-methoxy of vinyl
Base oxethyl) mixing that is formed with weight ratio 3.5:2.2:1 of silane and γ-methacryloxypropyl trimethoxy silane
Object.
In the step B, organosiloxane monomer is by phenyl siloxane monomer, cyclic siloxane monomer and vinyl silicon
The mixture that oxygen alkane monomer is formed with weight ratio 7:5:0.8;
The phenyl siloxane monomer is ethynyl phenyl diethoxy silane, propinyl diethylamino phenyl oxysilane, first
Base diphenyl Ethoxysilane, ethyl diphenyl Ethoxysilane, propyl diphenyl Ethoxysilane, vinyl diphenyl ethoxy
Base silane, acrylic diphenyl Ethoxysilane, acetenyl diphenyl Ethoxysilane, propinyl diphenyl Ethoxysilane,
3,5-dimethylphenyl Ethoxysilane, diethyl phenyl Ethoxysilane or dipropyl phenyl ethoxy silane.
The cyclic siloxane monomer is tetrahydro tetramethyl-ring tetrasiloxane, tetramethyl tetraethyl cyclotetrasiloxane, tetramethyl
Base tetraphenyl cyclotetrasiloxane, tetraethyl tetraphenyl cyclotetrasiloxane, t etram-ethyltetravinylcyclotetrasiloxane, tetravinyl four
Phenyl cyclotetrasiloxane, diethyl hexamethyl cyclotetrasiloxane, dimethyl Hexaethyl cyclotetrasiloxane or divinyl hexamethyl
Cyclotetrasiloxane.
The vinylsiloxane monomer is γ-mercapto propyl methyl dimethoxy silane, γ-methacryloxy third
Ylmethoxy dimethylsilane, γ-methacryloxypropyl dimethoxymethylsilane, γ-methacryloxy third
Base trimethoxy silane, γ-methacryloxypropyl ethyoxyl dimethylsilane or γ-methacryloxypropyl two
(ethoxymethyl) base silane.
In the step B, catalyst is toluenesulfonic acid, ethyl phenenyl azochlorosulfonate acid or acid dimethyl;
In the step B, step C1 and step D2, emulsifier is by cationic surfactant, anion surface active
The mixture that agent and nonionic surfactant are formed with weight ratio 0.7:1:0.5;
In the step C2 and the step D2, cladding monomer is by α-methylstyrene, methacrylonitrile, acrylic acid 2-
Ethylhexyl, isobornyl methacrylate, fumaric acid and N- methylmaleimido are with weight ratio 2.2:1.8:1.2:1:
The mixture of 0.5:0.3 composition;
In the step C2 and the step D2, initiator is by isopropyl benzene hydroperoxide, azodiisobutyronitrile and tetrem
The mixture that alkene imines is formed with weight ratio 1:1.2:2.2;
In the step D1, the average molecular weight of PTFE emulsion is 8,000,000, and solid content is 61%, and emulsion particle diameter is in 0.2 μ
M, viscosity 30*10-3Pa.S。
In the step D1, dispersing agent is organic dispersing agent;
The organic dispersing agent is that synthesis high score subclass dispersing agent or class containing carboxyl synthesize macromolecule dispersing agent;
The synthesis high score subclass dispersing agent is hydroxyl class partial alcoholysis polyvinyl alcohol;The class containing carboxyl synthesizes high score
Sub- dispersing agent is phenylethylene/maleic anhydride copolymer, vinyl acetate/copolymer-maleic anhydride and acrylic copolymer or methyl
Acrylic copolymer.
A kind of organic silicon fibre retardant containing PTFE and nano silica, the organic silicon fibre retardant is according to described above
Preparation method is made.
It is a kind of using anti-flaming polycarbonate made from the organic silicon fibre retardant described above containing PTFE and nano silica
Ester material, the flame-retardant polycarbonate material include the raw material of following parts by weight: 110 parts of polycarbonate, has 35 parts of glass fibre
0.8 part of machine silicon fire retardant, 7 parts of modifying agent, 8 parts of other auxiliary agents;
Wherein, the modifying agent is more created by macromolecule modified nanometer calcium carbonate, hyperbranched polyester amide and 4- allyl
The mixture that the wooden phenol modified dimethyl polysiloxane is formed with weight ratio 5:0.8:1.2.
The preparation method of the macromolecule modified nanometer calcium carbonate includes the following steps:
(1) 22g nanometer calcium carbonate and 0.6g calgon dispersing agent are added into 450mL distilled water, disperses 26h;Together
When 80g Polymeric quaternary ammonium salts are dissolved in 350mL tetrahydrofuran, dispersion 26h it is spare;
(2) 350mL tetrahydrofuran, high speed dispersion 0.6h, then slurry are added into scattered nanometer calcium carbonate system
Liquid is transferred in there-necked flask, and polymeric quartenary ammonium salting liquid is slowly added dropwise under stirring, and system constantly generates white flock precipitate;
(3) after completion of dropwise addition, system is warming up to 82 DEG C, after reacting 26h, then slurries is filtered, 62 DEG C of vacuum drying 42h,
Obtain macromolecule modified nanometer calcium carbonate;
Wherein, in the step (1), Polymeric quaternary ammonium salts are chlorination -2- hydroxyl -3- (dimethylamino) propyl polycyclic oxygen second
Alkoxy cellulose ether.
The synthetic method of the hyperbranched polyester amide are as follows: under nitrogen protection, successively by 1.1mol triethanolamine,
1.1mol1,2,4- trimellitic anhydride and 0.012mol Catalyzed by p-Toluenesulfonic Acid agent are added three neck round bottom flask and are placed in heating
In oil bath, stirring is gradually warming up to 225 DEG C, after raw material is uniformly mixed bleach, continues to be stirred to react at a temperature of 225 DEG C
3.5h is then cooled to room temperature, and obtains yellow transparent solid body i.e. hyperbranched polyester amide.
The synthetic method of the 4- allyl guaiacol modified dimethyl polysiloxane are as follows: equipped with thermometer, stirring
In the there-necked flask of device, 260g dimethyl silicone polymer, 26g 4- allyl guaiacol are sequentially added at room temperature, is formed after stirring
The suspension of White-opalescent;Add the octanol solution for the chloroplatinic acid that 0.9mL platinum mass fraction is 2.2%;Continue to stir, lead to
It is warming up to 98 DEG C under nitrogen, reacts 3.5h.
The melt index of the polycarbonate is bisphenol A polycarbonate of the melt index in 40g/10min;The glass
Fiber be fibre diameter 12 μm, fibre length 8mm alkali-free short glass fiber;Other described auxiliary agents are smoke suppressant.
Embodiment 5
A kind of preparation method of the organic silicon fibre retardant containing PTFE and nano silica, includes the following steps:
A, Nano-meter SiO_22Surface it is modified:
A1, configuration ethanol/water solution, are added Nano-meter SiO_22Particle, the high speed shear under the revolving speed of 4000rpm;Wherein, second
The volume ratio of alcohol and water is 10:1, Nano-meter SiO_22The dosage of particle is the 10% of ethanol/water solution quality;
A2, silane coupling agent is added, adding oxalic acid solution makes the pH value of reaction system 4, after reacting 2.5h, filter,
Washing, the Nano-meter SiO_2 modified up to surface after dry2Particle;Wherein, the dosage of silane coupling agent is Nano-meter SiO_22Mass particle
10%;
B, the synthesis of organopolysiloxane core lotion:
Organosiloxane monomer is uniformly mixed, is added in the aqueous solution dissolved with catalyst and emulsifier, at 80 DEG C
At a temperature of react 5h, obtain organopolysiloxane core lotion;Wherein, the gross mass of organosiloxane monomer is water quality
60%, the dosage of catalyst is the 5% of organosiloxane monomer mass, and the dosage of emulsifier is organosiloxane monomer mass
20%;
C, hydridization organic matter/Nano-meter SiO_22The preparation of lotion:
C1, it takes emulsifier soluble in water, the Nano-meter SiO_2 modified by surface is added2Particle is dispersed using ultrasonic wave
30min obtains dispersion liquid;Wherein, the dosage of emulsifier is the 20% of water quality, by the modified Nano-meter SiO_2 in surface2Particle
Dosage is the 10% of water quality;
C2, then dispersion liquid is added in organopolysiloxane core lotion, cladding monomer and initiator is added, caused poly-
Reaction is closed, hydridization organic matter/Nano-meter SiO_2 is obtained2Lotion;Wherein, the dosage of dispersion liquid is organopolysiloxane core quality of the emulsion
50%, the dosage for coating monomer is the 70% of organopolysiloxane core quality of the emulsion, and the dosage of initiator is organic poly- silicon oxygen
The 0.8% of alkane core quality of the emulsion;
D, contain PTFE and Nano-meter SiO_22Organic silicon fibre retardant preparation:
D1, by hydridization organic matter/Nano-meter SiO_22Lotion, PTFE emulsion, dispersing agent and distilled water are added to reaction kettle together
In, the high shear agitation 5min under 2000rpm revolving speed;Wherein, the dosage of PTFE emulsion is hydridization organic matter/Nano-meter SiO_22Cream
The 50% of liquid quality, the dosage of dispersing agent are hydridization organic matter/Nano-meter SiO_22The 5% of quality of the emulsion;
D2, cladding monomer is added, adds emulsifier and initiator, reacts 6h at a temperature of 80 DEG C;Wherein, monomer is coated
Dosage be hydridization organic matter/Nano-meter SiO_22The 70% of quality of the emulsion, the dosage of emulsifier are hydridization organic matter/Nano-meter SiO_22Cream
The 20% of liquid quality, the dosage of initiator are hydridization organic matter/Nano-meter SiO_22The 0.8% of quality of the emulsion;
D3, reaction product washed, is centrifuged, drying drying, the having containing PTFE and nano silica is made
Machine silicon fire retardant;
Wherein, in the step A2, silane coupling agent is by 3- aminopropyl trimethoxysilane, three (beta-methoxy of vinyl
Base oxethyl) mixture that is formed with weight ratio 4:2.5:1 of silane and γ-methacryloxypropyl trimethoxy silane.
In the step B, organosiloxane monomer is by phenyl siloxane monomer, cyclic siloxane monomer and vinyl silicon
The mixture that oxygen alkane monomer is formed with weight ratio 8:6:1.0;
The phenyl siloxane monomer is divinyl phenyl ethoxy silane, diallyl phenyl ethoxy silane, two
Ethynyl phenyl Ethoxysilane, dipropyl alkynyl phenyl Ethoxysilane, Methylethyl phenyl ethoxy silane, methyl-propyl benzene
Base oxethyl silane, ethyl propyl phenyl ethoxy silane, methyl vinyl phenyl Ethoxysilane, ethyl propylene base phenyl second
Oxysilane, methylacetylenyl phenyl ethoxy silane or ethyl propinyl phenyl ethoxy silane.
The cyclic siloxane monomer be six vinyl cyclotetrasiloxane of dimethyl, diphenyl hexamethyl cyclotetrasiloxane,
Dimethyl hexaphenyl cyclotetrasiloxane, vinyl heptamethylcyclotetrasiloxane, seven vinyl cyclotetrasiloxane of methyl, seven first of phenyl
Seven phenyl cyclotetrasiloxane of basic ring tetrasiloxane or methyl.
The vinylsiloxane monomer is γ-methacryloxypropyl morpholine silane, γ-methyl-prop
Alkene acryloxypropylethoxysilane dimethoxy-ethyl silane, γ-methacryloxypropyl ethyoxyl diethylsilane, γ-methyl-prop
Alkene acryloxypropylethoxysilane diethoxy ethylsilane or γ-methacryloxypropyl.
In the step B, catalyst is diethylbenzene sulfonic acid or dodecyl benzene sulfonic acid;
In the step B, step C1 and step D2, emulsifier is by cationic surfactant, anion surface active
The mixture that agent and nonionic surfactant are formed with weight ratio 0.8:1:0.6;
In the step C2 and the step D2, cladding monomer is by α-methylstyrene, methacrylonitrile, acrylic acid 2-
Ethylhexyl, isobornyl methacrylate, fumaric acid and N- methylmaleimido are with weight ratio 2.5:2:1.5:1:0.8:
The mixture of 0.6 composition;
In the step C2 and the step D2, initiator is by isopropyl benzene hydroperoxide, azodiisobutyronitrile and tetrem
The mixture that alkene imines is formed with weight ratio 1:1.5:2.5;
In the step D1, the average molecular weight of PTFE emulsion is 10,000,000, and solid content is 62%, and emulsion particle diameter is 0.30
μm, viscosity 40*10-3Pa.S。
In the step D1, dispersing agent is organic dispersing agent;
The organic dispersing agent is that nitrogenous class synthesizes macromolecule dispersing agent or ester-containing base class synthesizes macromolecule dispersing agent;
The nitrogenous class synthesis macromolecule dispersing agent is polyvinylpyrrolidone;The ester-containing base class synthesis macromolecule point
Powder is polyethyleneoxide fatty acid esters or sorbitan fatty acid.
A kind of organic silicon fibre retardant containing PTFE and nano silica, the organic silicon fibre retardant is according to described above
Preparation method is made.
It is a kind of using anti-flaming polycarbonate made from the organic silicon fibre retardant described above containing PTFE and nano silica
Ester material, the flame-retardant polycarbonate material include the raw material of following parts by weight: 120 parts of polycarbonate, has 40 parts of glass fibre
1.0 parts of machine silicon fire retardant, 8 parts of modifying agent, 10 parts of other auxiliary agents;
Wherein, the modifying agent is more created by macromolecule modified nanometer calcium carbonate, hyperbranched polyester amide and 4- allyl
The mixture that the wooden phenol modified dimethyl polysiloxane is formed with weight ratio 6:1.0:1.5.
The preparation method of the macromolecule modified nanometer calcium carbonate includes the following steps:
(1) 25g nanometer calcium carbonate and 0.7g calgon dispersing agent are added into 500mL distilled water, disperses 28h;Together
When 100g Polymeric quaternary ammonium salts are dissolved in 400mL tetrahydrofuran, dispersion 28h it is spare;
(2) 400mL tetrahydrofuran, high speed dispersion 0.7h, then slurry are added into scattered nanometer calcium carbonate system
Liquid is transferred in there-necked flask, and polymeric quartenary ammonium salting liquid is slowly added dropwise under stirring, and system constantly generates white flock precipitate;
(3) after completion of dropwise addition, system is warming up to 85 DEG C, after reacting 28h, then slurries is filtered, 65 DEG C of vacuum drying 48h,
Obtain macromolecule modified nanometer calcium carbonate;
Wherein, in the step (1), Polymeric quaternary ammonium salts N, N, N- trimethyl-2- (2- methyl-1-oxo-2- propylene
Base oxygroup) ethyl ammonium chloride-acrylamide copolymer.
The synthetic method of the hyperbranched polyester amide are as follows: under nitrogen protection, successively by 1.2mol triethanolamine,
1.2mol1,2,4- trimellitic anhydride and 0.015mol Catalyzed by p-Toluenesulfonic Acid agent are added three neck round bottom flask and are placed in heating
In oil bath, stirring is gradually warming up to 230 DEG C, after raw material is uniformly mixed bleach, continues to be stirred to react at a temperature of 230 DEG C
4h is then cooled to room temperature, and obtains yellow transparent solid body i.e. hyperbranched polyester amide.
The synthetic method of the 4- allyl guaiacol modified dimethyl polysiloxane are as follows: equipped with thermometer, stirring
In the there-necked flask of device, 270g dimethyl silicone polymer, 27g 4- allyl guaiacol are sequentially added at room temperature, is formed after stirring
The suspension of White-opalescent;Add the octanol solution for the chloroplatinic acid that 1.0mL platinum mass fraction is 2.5%;Continue to stir, lead to
It is warming up to 100 DEG C under nitrogen, reacts 4h.
The melt index of the polycarbonate is polyester-type polycarbonate of the melt index in 50g/10min;The glass
Fiber be fibre diameter 15 μm, fibre length 10mm alkali-free short glass fiber;Other described auxiliary agents are Vitrified powder.
Embodiment 6
The present embodiment and above-described embodiment 1 the difference is that:
The phenyl siloxane monomer is by aminomethyl phenyl dimethoxysilane and aminomethyl phenyl diethoxy silane with weight
Measure the mixture formed than 2:1.
The cyclic siloxane monomer is by trimethyl triethyl group cyclotrisiloxane, six vinyl cyclotetrasiloxane of dimethyl
The mixture formed with seven phenyl cyclotetrasiloxane of methyl with weight ratio 2:0.5:1.
The vinylsiloxane monomer is by vinyl propyldimethoxy-silane, to vinyl phenylmethyl ethyoxyl
The mixture that silane and 3- (to vinylbenzoyl oxygroup) hydroxypropyl methyl diethoxy silane are formed with weight ratio 2:1.5:1.
The catalyst is by methylol sulfonic acid, trifluoroethyl sulfonic acid and hydroxypropyl sulfonic acid with weight ratio 1:0.8:0.4 group
At mixture.
The cationic surfactant is by dialkyl dimethyl quaternary ammonium salt, benzalkonium dimethyl quaternary ammonium and single alkane
The mixture that based quaternary ammonium salt is formed with weight ratio 1:1.2:1.8;The anionic surfactant is by polyoxyethylene alkyl ether
The mixture that hydrogen sulfuric acid ester, alkyl diphenyl base ether disulfonate and polyoxyethylene alkyl ether ester are formed with weight ratio 1:0.5:1.4;
The nonionic surfactant is by isomeric alcohol polyethenoxy ether, sorbitan fatty acid esters and polyoxyethylene hardened castor
The mixture that sesame oil aliphatic ester is formed with weight ratio 1.6:1:0.8.
The dispersing agent is by diatomite, calcium carbonate, methylhydroxypropylcellulose and sorbitan fatty acid with weight
Measure the mixture formed than 1:0.5:1:0.8.
The Polymeric quaternary ammonium salts are by brominated polyphenylether stearyl dimethyl benzyl ammonium chloride, chlorination -2- hydroxyl -3-
(dimethylamino) propyl polyethylene oxide cellulose ether and N, N, N- trimethyl-2- (2- methyl-1-oxo-2- acrylic oxygroup)
The mixture that ethyl ammonium chloride-acrylamide copolymer is formed with weight ratio 2:1.5:1.
The polycarbonate is by bisphenol A polycarbonate, polyester-type polycarbonate and hexamethylene bisphenol A polycarbonate
The mixture formed with weight ratio 1:0.8:1.
Other described auxiliary agents are by antioxidant, UV resistant agent, lubricant, smoke suppressant and Vitrified powder with weight ratio 0.4:
The mixture of 0.6:1:0.5:0.8 composition.
The antioxidant is by β-(3,5- di-tert-butyl-hydroxy phenyl) propionic acid n-octadecyl alcohol ester, three [bis- uncles of 2.4-
Butyl phenyl] mixture that is formed with weight ratio 1:0.8:1 of the double lauryls of phosphite ester and thio-2 acid.
The UV resistant agent is by 2- (2 '-hydroxyls -5 '-aminomethyl phenyl) benzotriazole, 2- hydroxyl -4- methoxyl group two
The mixture that Benzophenone and hexamethylphosphoramide are formed with weight ratio 0.5:1.4:1.
The lubricant is by oxidized polyethylene wax, glycerin monostearate and stearic amide with weight ratio 1:0.4:1
The mixture of composition.
The mixing that the smoke suppressant is made of ferrocene, antimony oxide and ammonium octamolybdate with weight ratio 0.5:1.5:1
Object.
The mixing that the Vitrified powder is made of attapulgite, zinc borate, silicate glass powder with weight ratio 2:0.5:1
Object.
Embodiment 7
The present embodiment and above-described embodiment 2 the difference is that:
The phenyl siloxane monomer is by aminomethyl phenyl dimethoxysilane and aminomethyl phenyl diethoxy silane with weight
Measure the mixture formed than 2.5:1.
The cyclic siloxane monomer is by trimethyl triethyl group cyclotrisiloxane, six vinyl cyclotetrasiloxane of dimethyl
The mixture formed with seven phenyl cyclotetrasiloxane of methyl with weight ratio 2.5:0.8:1.
The vinylsiloxane monomer is by vinyl propyldimethoxy-silane, to vinyl phenylmethyl ethyoxyl
The mixing that silane and 3- (to vinylbenzoyl oxygroup) hydroxypropyl methyl diethoxy silane are formed with weight ratio 2.5:1.8:1
Object.
The catalyst is by methylol sulfonic acid, trifluoroethyl sulfonic acid and hydroxypropyl sulfonic acid with weight ratio 1:0.9:0.5 group
At mixture.
The cationic surfactant is by dialkyl dimethyl quaternary ammonium salt, benzalkonium dimethyl quaternary ammonium and single alkane
The mixture that based quaternary ammonium salt is formed with weight ratio 1:1.3:2;The anionic surfactant is by polyoxyethylene alkyl ether sulphur
The mixture that sour hydrogen ester, alkyl diphenyl base ether disulfonate and polyoxyethylene alkyl ether ester are formed with weight ratio 1:0.8:1.6;Institute
Stating nonionic surfactant is by isomeric alcohol polyethenoxy ether, sorbitan fatty acid esters and polyoxyethylene hardened castor-oil plant
The mixture that oil and fat acid esters is formed with weight ratio 1.8:1:0.9.
The dispersing agent is by diatomite, calcium carbonate, methylhydroxypropylcellulose and sorbitan fatty acid with weight
Measure the mixture formed than 1.2:0.8:1:0.9.
The Polymeric quaternary ammonium salts are by brominated polyphenylether stearyl dimethyl benzyl ammonium chloride, chlorination -2- hydroxyl -3-
(dimethylamino) propyl polyethylene oxide cellulose ether and N, N, N- trimethyl-2- (2- methyl-1-oxo-2- acrylic oxygroup)
The mixture that ethyl ammonium chloride-acrylamide copolymer is formed with weight ratio 2.5:1.8:1.
The polycarbonate is by bisphenol A polycarbonate, polyester-type polycarbonate and hexamethylene bisphenol A polycarbonate
The mixture formed with weight ratio 1.2:0.9:1.
Other described auxiliary agents are by antioxidant, UV resistant agent, lubricant, smoke suppressant and Vitrified powder with weight ratio 0.5:
The mixture of 0.7:1:0.8:0.9 composition.
The antioxidant is by β-(3,5- di-tert-butyl-hydroxy phenyl) propionic acid n-octadecyl alcohol ester, three [bis- uncles of 2.4-
Butyl phenyl] mixture that is formed with weight ratio 1.2:0.9:1 of the double lauryls of phosphite ester and thio-2 acid.
The UV resistant agent is by 2- (2 '-hydroxyls -5 '-aminomethyl phenyl) benzotriazole, 2- hydroxyl -4- methoxyl group two
The mixture that Benzophenone and hexamethylphosphoramide are formed with weight ratio 0.8:1.6:1.
The lubricant is by oxidized polyethylene wax, glycerin monostearate and stearic amide with weight ratio 1.2:0.5:
The mixture of 1 composition.
The mixing that the smoke suppressant is made of ferrocene, antimony oxide and ammonium octamolybdate with weight ratio 0.8:1.8:1
Object.
The mixing that the Vitrified powder is made of attapulgite, zinc borate, silicate glass powder with weight ratio 2.5:0.8:1
Object.
Embodiment 8
The present embodiment and above-described embodiment 3 the difference is that:
The phenyl siloxane monomer is by aminomethyl phenyl dimethoxysilane and aminomethyl phenyl diethoxy silane with weight
Measure the mixture formed than 3:1.
The cyclic siloxane monomer is by trimethyl triethyl group cyclotrisiloxane, six vinyl cyclotetrasiloxane of dimethyl
The mixture formed with seven phenyl cyclotetrasiloxane of methyl with weight ratio 3:1:1.
The vinylsiloxane monomer is by vinyl propyldimethoxy-silane, to vinyl phenylmethyl ethyoxyl
The mixture that silane and 3- (to vinylbenzoyl oxygroup) hydroxypropyl methyl diethoxy silane are formed with weight ratio 3:2:1.
The catalyst is made of methylol sulfonic acid, trifluoroethyl sulfonic acid and hydroxypropyl sulfonic acid with weight ratio 1:1:0.6
Mixture.
The cationic surfactant is by dialkyl dimethyl quaternary ammonium salt, benzalkonium dimethyl quaternary ammonium and single alkane
The mixture that based quaternary ammonium salt is formed with weight ratio 1:1.4:2.2;The anionic surfactant is by polyoxyethylene alkyl ether
The mixture that hydrogen sulfuric acid ester, alkyl diphenyl base ether disulfonate and polyoxyethylene alkyl ether ester are formed with weight ratio 1:1:1.8;Institute
Stating nonionic surfactant is by isomeric alcohol polyethenoxy ether, sorbitan fatty acid esters and polyoxyethylene hardened castor-oil plant
The mixture that oil and fat acid esters is formed with weight ratio 2:1:1.
The dispersing agent is by diatomite, calcium carbonate, methylhydroxypropylcellulose and sorbitan fatty acid with weight
Measure the mixture formed than 1.5:1:1:1.
The Polymeric quaternary ammonium salts are by brominated polyphenylether stearyl dimethyl benzyl ammonium chloride, chlorination -2- hydroxyl -3-
(dimethylamino) propyl polyethylene oxide cellulose ether and N, N, N- trimethyl-2- (2- methyl-1-oxo-2- acrylic oxygroup)
The mixture that ethyl ammonium chloride-acrylamide copolymer is formed with weight ratio 3:2:1.
The polycarbonate is by bisphenol A polycarbonate, polyester-type polycarbonate and hexamethylene bisphenol A polycarbonate
The mixture formed with weight ratio 1.5:1:1.
Other described auxiliary agents are by antioxidant, UV resistant agent, lubricant, smoke suppressant and Vitrified powder with weight ratio 0.6:
The mixture of 0.8:1:1:1 composition.
The antioxidant is by β-(3,5- di-tert-butyl-hydroxy phenyl) propionic acid n-octadecyl alcohol ester, three [bis- uncles of 2.4-
Butyl phenyl] mixture that is formed with weight ratio 1.5:1:1 of the double lauryls of phosphite ester and thio-2 acid.
The UV resistant agent is by 2- (2 '-hydroxyls -5 '-aminomethyl phenyl) benzotriazole, 2- hydroxyl -4- methoxyl group two
The mixture that Benzophenone and hexamethylphosphoramide are formed with weight ratio 1:1.8:1.
The lubricant is by oxidized polyethylene wax, glycerin monostearate and stearic amide with weight ratio 1.5:0.6:
The mixture of 1 composition.
The mixture that the smoke suppressant is made of ferrocene, antimony oxide and ammonium octamolybdate with weight ratio 1:2:1.
The mixture that the Vitrified powder is made of attapulgite, zinc borate, silicate glass powder with weight ratio 3:1:1.
Embodiment 9
The present embodiment and above-described embodiment 4 the difference is that:
The phenyl siloxane monomer is by aminomethyl phenyl dimethoxysilane and aminomethyl phenyl diethoxy silane with weight
Measure the mixture formed than 3.5:1.
The cyclic siloxane monomer is by trimethyl triethyl group cyclotrisiloxane, six vinyl cyclotetrasiloxane of dimethyl
The mixture formed with seven phenyl cyclotetrasiloxane of methyl with weight ratio 3.5:1.2:1.
The vinylsiloxane monomer is by vinyl propyldimethoxy-silane, to vinyl phenylmethyl ethyoxyl
The mixing that silane and 3- (to vinylbenzoyl oxygroup) hydroxypropyl methyl diethoxy silane are formed with weight ratio 3.5:2.2:1
Object.
The catalyst is by methylol sulfonic acid, trifluoroethyl sulfonic acid and hydroxypropyl sulfonic acid with weight ratio 1:1.1:0.7 group
At mixture.
The cationic surfactant is by dialkyl dimethyl quaternary ammonium salt, benzalkonium dimethyl quaternary ammonium and single alkane
The mixture that based quaternary ammonium salt is formed with weight ratio 1:1.5:2.4;The anionic surfactant is by polyoxyethylene alkyl ether
The mixture that hydrogen sulfuric acid ester, alkyl diphenyl base ether disulfonate and polyoxyethylene alkyl ether ester are formed with weight ratio 1:1.2:2;Institute
Stating nonionic surfactant is by isomeric alcohol polyethenoxy ether, sorbitan fatty acid esters and polyoxyethylene hardened castor-oil plant
The mixture that oil and fat acid esters is formed with weight ratio 2.2:1:1.1.
The dispersing agent is by diatomite, calcium carbonate, methylhydroxypropylcellulose and sorbitan fatty acid with weight
Measure the mixture formed than 1.8:1.2:1:1.1.
The Polymeric quaternary ammonium salts are by brominated polyphenylether stearyl dimethyl benzyl ammonium chloride, chlorination -2- hydroxyl -3-
(dimethylamino) propyl polyethylene oxide cellulose ether and N, N, N- trimethyl-2- (2- methyl-1-oxo-2- acrylic oxygroup)
The mixture that ethyl ammonium chloride-acrylamide copolymer is formed with weight ratio 3.5:2.2:1.
The polycarbonate is by bisphenol A polycarbonate, polyester-type polycarbonate and hexamethylene bisphenol A polycarbonate
The mixture formed with weight ratio 1.8:1.1:1.
Other described auxiliary agents are by antioxidant, UV resistant agent, lubricant, smoke suppressant and Vitrified powder with weight ratio 0.7:
The mixture of 0.9:1:1.2:1.1 composition.
The antioxidant is by β-(3,5- di-tert-butyl-hydroxy phenyl) propionic acid n-octadecyl alcohol ester, three [bis- uncles of 2.4-
Butyl phenyl] mixture that is formed with weight ratio 1.8:1.1:1 of the double lauryls of phosphite ester and thio-2 acid.
The UV resistant agent is by 2- (2 '-hydroxyls -5 '-aminomethyl phenyl) benzotriazole, 2- hydroxyl -4- methoxyl group two
The mixture that Benzophenone and hexamethylphosphoramide are formed with weight ratio 1.2:2:1.
The lubricant is by oxidized polyethylene wax, glycerin monostearate and stearic amide with weight ratio 1.8:0.7:
The mixture of 1 composition.
The mixing that the smoke suppressant is made of ferrocene, antimony oxide and ammonium octamolybdate with weight ratio 1.2:2.2:1
Object.
The mixing that the Vitrified powder is made of attapulgite, zinc borate, silicate glass powder with weight ratio 3.5:1.2:1
Object.
Embodiment 10
The present embodiment and above-described embodiment 5 the difference is that:
The phenyl siloxane monomer is by aminomethyl phenyl dimethoxysilane and aminomethyl phenyl diethoxy silane with weight
Measure the mixture formed than 4:1.
The cyclic siloxane monomer is by trimethyl triethyl group cyclotrisiloxane, six vinyl cyclotetrasiloxane of dimethyl
The mixture formed with seven phenyl cyclotetrasiloxane of methyl with weight ratio 4:1.5:1.
The vinylsiloxane monomer is by vinyl propyldimethoxy-silane, to vinyl phenylmethyl ethyoxyl
The mixture that silane and 3- (to vinylbenzoyl oxygroup) hydroxypropyl methyl diethoxy silane are formed with weight ratio 4:2.5:1.
The catalyst is by methylol sulfonic acid, trifluoroethyl sulfonic acid and hydroxypropyl sulfonic acid with weight ratio 1:1.2:0.8 group
At mixture.
The cationic surfactant is by dialkyl dimethyl quaternary ammonium salt, benzalkonium dimethyl quaternary ammonium and single alkane
The mixture that based quaternary ammonium salt is formed with weight ratio 1:1.6:2.6;The anionic surfactant is by polyoxyethylene alkyl ether
The mixture that hydrogen sulfuric acid ester, alkyl diphenyl base ether disulfonate and polyoxyethylene alkyl ether ester are formed with weight ratio 1:1.5:2.2;
The nonionic surfactant is by isomeric alcohol polyethenoxy ether, sorbitan fatty acid esters and polyoxyethylene hardened castor
The mixture that sesame oil aliphatic ester is formed with weight ratio 2.4:1:1.2.
The dispersing agent is by diatomite, calcium carbonate, methylhydroxypropylcellulose and sorbitan fatty acid with weight
Measure the mixture formed than 2:1.5:1:1.2.
The Polymeric quaternary ammonium salts are by brominated polyphenylether stearyl dimethyl benzyl ammonium chloride, chlorination -2- hydroxyl -3-
(dimethylamino) propyl polyethylene oxide cellulose ether and N, N, N- trimethyl-2- (2- methyl-1-oxo-2- acrylic oxygroup)
The mixture that ethyl ammonium chloride-acrylamide copolymer is formed with weight ratio 4:2.5:1.
The polycarbonate is by bisphenol A polycarbonate, polyester-type polycarbonate and hexamethylene bisphenol A polycarbonate
The mixture formed with weight ratio 2:1.2:1.
Other described auxiliary agents are by antioxidant, UV resistant agent, lubricant, smoke suppressant and Vitrified powder with weight ratio 0.8:
1.0:1:1.5:1.2 the mixture of composition.
The antioxidant is by β-(3,5- di-tert-butyl-hydroxy phenyl) propionic acid n-octadecyl alcohol ester, three [bis- uncles of 2.4-
Butyl phenyl] mixture that is formed with weight ratio 2:1.2:1 of the double lauryls of phosphite ester and thio-2 acid.
The UV resistant agent is by 2- (2 '-hydroxyls -5 '-aminomethyl phenyl) benzotriazole, 2- hydroxyl -4- methoxyl group two
The mixture that Benzophenone and hexamethylphosphoramide are formed with weight ratio 1.5:2.2:1.
The lubricant is by oxidized polyethylene wax, glycerin monostearate and stearic amide with weight ratio 2:0.8:1
The mixture of composition.
The mixing that the smoke suppressant is made of ferrocene, antimony oxide and ammonium octamolybdate with weight ratio 1.5:2.5:1
Object.
The mixing that the Vitrified powder is made of attapulgite, zinc borate, silicate glass powder with weight ratio 4:1.5:1
Object.
After tested, organic silicon fibre retardant made from embodiment 1-10 is applied in polycarbonate, and organosilicon resistance both can be improved
The resistance to thermal decomposition temperature of agent is fired, and makes fire retardant that there is anti-dripping effects, also improves the flame retardant property of organic silicon fibre retardant, is hindered
Combustion performance test can achieve 1.6mmUL94V-0 grades, and good flame retardation effect, it is 2-4s that anti-dripping melt, which tests t1, and t2 2-4s does not have
Dropping ignites absorbent cotton, reaches V0 standard.
Above-described embodiment is the preferable implementation of the present invention, and in addition to this, the present invention can be realized with other way,
Do not depart under the premise of present inventive concept it is any obviously replace it is within the scope of the present invention.
Claims (10)
1. a kind of preparation method of the organic silicon fibre retardant containing PTFE and nano silica, it is characterised in that: including walking as follows
It is rapid:
A, Nano-meter SiO_22Surface it is modified:
A1, configuration ethanol/water solution, are added Nano-meter SiO_22Particle, the high speed shear under the revolving speed of 3000-4000rpm;
A2, silane coupling agent is added, adding oxalic acid solution makes the pH value of reaction system in 3-4, after reacting 1.5-2.5h, takes out
Filter, washing, the Nano-meter SiO_2 modified up to surface after dry2Particle;
B, the synthesis of organopolysiloxane core lotion:
Organosiloxane monomer is uniformly mixed, is added in the aqueous solution dissolved with catalyst and emulsifier, at 30~80 DEG C
At a temperature of react 5~10h, obtain organopolysiloxane core lotion;
C, hydridization organic matter/Nano-meter SiO_22The preparation of lotion:
C1, it takes emulsifier soluble in water, the Nano-meter SiO_2 modified by surface is added2Particle disperses 10-30min using ultrasonic wave,
Obtain dispersion liquid;
C2, then dispersion liquid is added in organopolysiloxane core lotion, cladding monomer and initiator is added, it is anti-to cause polymerization
It answers, obtains hydridization organic matter/Nano-meter SiO_22Lotion;
D, contain PTFE and Nano-meter SiO_22Organic silicon fibre retardant preparation:
D1, by hydridization organic matter/Nano-meter SiO_22Lotion, PTFE emulsion, dispersing agent and distilled water are added in reaction kettle together,
5~25min of high shear agitation under 1000~2000rpm revolving speed;
D2, cladding monomer is added, adds emulsifier and initiator, reacts 6-10h at a temperature of 50~80 DEG C;
D3, reaction product washed, is centrifuged, drying drying, the organosilicon containing PTFE and nano silica is made
Fire retardant;
Wherein, in the step A2, silane coupling agent is by 3- aminopropyl trimethoxysilane, (the 'beta '-methoxy second of vinyl three
Oxygroup) mixing that is formed with weight ratio 2-4:1.5-2.5:1 of silane and γ-methacryloxypropyl trimethoxy silane
Object.
2. a kind of preparation method of organic silicon fibre retardant containing PTFE and nano silica according to claim 1,
Be characterized in that: in the step B, organosiloxane monomer is by phenyl siloxane monomer, cyclic siloxane monomer and vinyl
The mixture that siloxanyl monomers are formed with weight ratio 4-8:2-6:0.1-1.0;
The structural formula of the phenyl siloxane monomer are as follows:Wherein, R1、R2、R3And R4Respectively hydrogen, methyl,
Any one in ethyl, propyl, vinyl, acrylic, acetenyl, propinyl, methoxyl group, ethyoxyl and phenyl, and R1、R2、
R3And R4In at least one be phenyl, at least one methoxy or ethoxy;
The structural formula of the polymerized monomer of the cyclic siloxane monomer isWherein R5And R6Respectively hydrogen,
Any one in methyl, ethyl, propyl, vinyl, acrylic, acetenyl, propinyl and phenyl, the annular siloxane list
Polymerization degree n=3-6 of body;
The structural formula of the vinylsiloxane monomer are as follows:Wherein, R7, R8, R9 and R10 are respectively hydrogen, first
Base, ethyl, propyl, vinyl, acrylic, styryl, γ-methacryloxypropyl, styryl, 2- are (to ethylene
Base phenyl) ethyl, in 3- (to vinylbenzoyl oxygroup) propyl, acetenyl, propinyl, methoxyl group, ethyoxyl and phenyl
Any one, and R7, R8, R9 and R10 at least one be vinyl, acrylic, styryl, γ-methacryloxy
Propyl, styryl, 2- (to ethenylphenyl) ethyl or 3- (to vinylbenzoyl oxygroup) propyl, at least one is first
Oxygroup or ethyoxyl.
3. a kind of preparation method of organic silicon fibre retardant containing PTFE and nano silica according to claim 1,
It is characterized in that: in the step B, the structural formula of catalyst are as follows:Wherein, R ' is the alkane that carbon atom number is 1-10
Base, alkenyl, aromatic radical or carbon atom number are the naphthenic base of 3-10, cycloalkenyl;
In the step B, step C1 and step D2, emulsifier be by cationic surfactant, anionic surfactant and
The mixture that nonionic surfactant is formed with weight ratio 0.4-0.8:1:0.2-0.6;
In the step C2 and the step D2, cladding monomer is by α-methylstyrene, methacrylonitrile, acrylic acid 2- ethyl
Own ester, isobornyl methacrylate, fumaric acid and N- methylmaleimido are with weight ratio 1.5-2.5:1-2:0.5-1.5:
1:0.4-0.8:0.2-0.6 the mixture of composition;
In the step C2 and the step D2, initiator is sub- by isopropyl benzene hydroperoxide, azodiisobutyronitrile and four ethylene
The mixture that amine is formed with weight ratio 1:0.5-1.5:1.5-2.5;
In the step D1, the average molecular weight of PTFE emulsion is 1,000,000-1,000 ten thousand, and solid content is in 58%-62%, lotion grain
Diameter is at 0.01-0.30 μm, viscosity 10-40*10-3Pa.S。
4. a kind of preparation method of organic silicon fibre retardant containing PTFE and nano silica according to claim 1,
Be characterized in that: in the step D1, dispersing agent is inorganic dispersing agent and/or organic dispersing agent;
The inorganic dispersing agent is natural silicate, Sulfates, carbonate, Oxalates, hydroxide species and oxidation
At least one of species;
The natural silicate is at least one of talcum, bentonite, diatomite and kaolin;The Sulfates are sulfuric acid
Calcium and/or barium sulfate;The carbonate is at least one of calcium carbonate, barium carbonate and magnesium carbonate;The Oxalates are
Calcium oxalate;The hydroxide species are at least one of aluminium hydroxide, magnesium hydroxide and calcium hydroxide;It is described oxide-based to be
Titanium dioxide and/or zinc oxide;
The organic dispersing agent is natural polymer subclass dispersing agent, protein-based macromolecule dispersing agent, cellulose derivative
Class dispersing agent, synthesis high score subclass dispersing agent, class containing carboxyl synthesis macromolecule dispersing agent, nitrogenous class synthesize macromolecule dispersing agent and
At least one of ester-containing base class synthesis macromolecule dispersing agent;
The natural polymer subclass dispersing agent is at least one of carbohydrate starch, pectin, natural plant gum and seaweed glue;The albumen
Matter class macromolecule dispersing agent is gelatin and/or Fish protein;The cellulose derivative class dispersing agent is methylcellulose, methyl
At least one of hydroxypropyl cellulose, hydroxyethyl cellulose and hydroxypropyl cellulose;The synthesis high score subclass dispersing agent is
Hydroxyl class partial alcoholysis polyvinyl alcohol;The class containing carboxyl synthesis macromolecule dispersing agent be phenylethylene/maleic anhydride copolymer,
Vinyl acetate/copolymer-maleic anhydride and at least one of acrylic copolymer and methacrylic copolymer;It is described
Nitrogenous class synthesis macromolecule dispersing agent is polyvinylpyrrolidone;The ester-containing base class synthesis macromolecule dispersing agent is polycyclic oxygen
Ethane aliphatic ester and/or sorbitan fatty acid.
5. a kind of organic silicon fibre retardant containing PTFE and nano silica, it is characterised in that: the organic silicon fibre retardant according to
The described in any item preparation methods of claim 1-4 are made.
6. fire-retardant poly- carbon made from a kind of organic silicon fibre retardant containing PTFE and nano silica using described in claim 5
Acid esters material, it is characterised in that: the flame-retardant polycarbonate material includes the raw material of following parts by weight:
Wherein, the modifying agent is by macromolecule modified nanometer calcium carbonate, hyperbranched polyester amide and 4- allyl guaiacol
The mixture that modified dimethyl polysiloxane is formed with weight ratio 2-6:0.1-1.0:0.5-1.5.
7. a kind of flame-retardant polycarbonate material according to claim 6, it is characterised in that: the macromolecule modified nano-sized carbon
The preparation method of sour calcium includes the following steps:
(1) 15-25g nanometer calcium carbonate and 0.3-0.7g calgon dispersing agent, dispersion are added into 300-500mL distilled water
20-28h;60-100g Polymeric quaternary ammonium salts are dissolved in 200-400mL tetrahydrofuran simultaneously, dispersion 20-28h is spare;
(2) the addition 200-400mL tetrahydrofuran into scattered nanometer calcium carbonate system, high speed dispersion 0.3-0.7h, then
Slurries are transferred in there-necked flask, polymeric quartenary ammonium salting liquid is slowly added dropwise under stirring, system constantly generates white flock precipitate;
(3) after completion of dropwise addition, system is warming up to 75-85 DEG C, after reacting 20-28h, then slurries is filtered, 55-65 DEG C of vacuum drying
24-48h obtains macromolecule modified nanometer calcium carbonate;
Wherein, in the step (1), Polymeric quaternary ammonium salts are brominated polyphenylether stearyl dimethyl benzyl ammonium chloride, diformazan
Base diallyl ammonium chloride-acrylamide copolymer, polydimethyl diallyl ammonium chloride, chlorination -2- hydroxyl -3- (front three ammonia
Base) propyl polyethylene oxide cellulose ether and N, N, N- trimethyl-2- (2- methyl-1-oxo-2- acrylic oxygroup) ethyl chloride
Change at least one of ammonium-acrylamide copolymer.
8. a kind of flame-retardant polycarbonate material according to claim 6, it is characterised in that: the hyperbranched polyester amide
Synthetic method are as follows: under nitrogen protection, successively by 0.8-1.2mol triethanolamine, 0.8-1.2mol 1,2,4- trimellitic anhydride
And 0.005-0.015mol Catalyzed by p-Toluenesulfonic Acid agent is added three neck round bottom flask and is placed in heating oil bath, stirring, gradually
It is warming up to 210-230 DEG C, after raw material is uniformly mixed bleach, continues to be stirred to react 2-4h at a temperature of 210-230 DEG C, then
It is cooled to room temperature, obtains yellow transparent solid body i.e. hyperbranched polyester amide.
9. a kind of flame-retardant polycarbonate material according to claim 6, it is characterised in that: the 4- allyl guaiacol
The synthetic method of modified dimethyl polysiloxane are as follows: in the there-necked flask equipped with thermometer, blender, sequentially add at room temperature
230-270g dimethyl silicone polymer, 23-27g 4- allyl guaiacol form the suspension of White-opalescent after stirring;
Add the octanol solution for the chloroplatinic acid that 0.5-1.0mL platinum mass fraction is 1.5-2.5%;Continue to stir, heat up under logical nitrogen
To 90-100 DEG C, 2-4h is reacted.
10. a kind of flame-retardant polycarbonate material according to claim 6, it is characterised in that: the melting of the polycarbonate
Index is that bisphenol A polycarbonate, polyester-type polycarbonate and hexamethylene bisphenol A-type of the melt index in 10-50g/10min are poly-
At least one of carbonic ester;The glass fibre is that fibre diameter is chopped in 5-15 μm, alkali-free of the fibre length in 1-10mm
Glass fibre;Other described auxiliary agents are at least one of antioxidant, UV resistant agent, lubricant, smoke suppressant and Vitrified powder.
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