CN1197913C - 阻燃性树脂组合物 - Google Patents
阻燃性树脂组合物 Download PDFInfo
- Publication number
- CN1197913C CN1197913C CN02130858.6A CN02130858A CN1197913C CN 1197913 C CN1197913 C CN 1197913C CN 02130858 A CN02130858 A CN 02130858A CN 1197913 C CN1197913 C CN 1197913C
- Authority
- CN
- China
- Prior art keywords
- organopolysiloxane
- unit
- metal salt
- resin
- aromatic polycarbonate
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
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- 239000011342 resin composition Substances 0.000 title claims abstract description 54
- 229920001296 polysiloxane Polymers 0.000 claims abstract description 156
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims abstract description 147
- 229920005989 resin Polymers 0.000 claims abstract description 123
- 239000011347 resin Substances 0.000 claims abstract description 123
- 150000003839 salts Chemical class 0.000 claims abstract description 117
- 229910052751 metal Inorganic materials 0.000 claims abstract description 103
- 239000002184 metal Substances 0.000 claims abstract description 103
- -1 siloxane unit Chemical group 0.000 claims abstract description 102
- 125000003118 aryl group Chemical group 0.000 claims abstract description 84
- 239000003063 flame retardant Substances 0.000 claims abstract description 83
- 229920000642 polymer Polymers 0.000 claims abstract description 82
- 239000004417 polycarbonate Substances 0.000 claims abstract description 80
- 229920000515 polycarbonate Polymers 0.000 claims abstract description 75
- 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 abstract description 58
- 239000000203 mixture Substances 0.000 claims abstract description 33
- 229910052784 alkaline earth metal Inorganic materials 0.000 claims abstract description 12
- 229910052783 alkali metal Inorganic materials 0.000 claims abstract description 10
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 claims description 82
- 239000011780 sodium chloride Substances 0.000 claims description 41
- 150000001875 compounds Chemical class 0.000 claims description 27
- 229920002554 vinyl polymer Polymers 0.000 claims description 14
- 230000009977 dual effect Effects 0.000 claims description 11
- 229910052500 inorganic mineral Inorganic materials 0.000 claims description 11
- 239000011707 mineral Substances 0.000 claims description 11
- JHJLBTNAGRQEKS-UHFFFAOYSA-M sodium bromide Chemical compound [Na+].[Br-] JHJLBTNAGRQEKS-UHFFFAOYSA-M 0.000 claims description 10
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 claims description 9
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 9
- 150000008045 alkali metal halides Chemical class 0.000 claims description 8
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 claims description 7
- 229910001508 alkali metal halide Inorganic materials 0.000 claims description 7
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 7
- 229910017604 nitric acid Inorganic materials 0.000 claims description 7
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 6
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 6
- 125000005041 acyloxyalkyl group Chemical group 0.000 claims description 5
- 229910001615 alkaline earth metal halide Inorganic materials 0.000 claims description 5
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 5
- 125000001188 haloalkyl group Chemical group 0.000 claims description 5
- 230000001588 bifunctional effect Effects 0.000 abstract 1
- 238000000034 method Methods 0.000 description 61
- 230000000052 comparative effect Effects 0.000 description 39
- 229920001971 elastomer Polymers 0.000 description 29
- 239000005060 rubber Substances 0.000 description 29
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 16
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 15
- 239000003054 catalyst Substances 0.000 description 15
- 230000000694 effects Effects 0.000 description 14
- 239000011734 sodium Substances 0.000 description 14
- 239000002253 acid Substances 0.000 description 13
- 238000004519 manufacturing process Methods 0.000 description 13
- 239000002904 solvent Substances 0.000 description 13
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 12
- 229910004298 SiO 2 Inorganic materials 0.000 description 11
- 239000000178 monomer Substances 0.000 description 11
- 239000002245 particle Substances 0.000 description 11
- 239000000126 substance Substances 0.000 description 11
- 238000005516 engineering process Methods 0.000 description 10
- 229920005668 polycarbonate resin Polymers 0.000 description 10
- 239000004431 polycarbonate resin Substances 0.000 description 10
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 9
- 239000011575 calcium Substances 0.000 description 9
- 239000011777 magnesium Substances 0.000 description 9
- 230000004048 modification Effects 0.000 description 8
- 238000012986 modification Methods 0.000 description 8
- 150000002989 phenols Chemical class 0.000 description 8
- 239000002994 raw material Substances 0.000 description 8
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 7
- 229910000041 hydrogen chloride Inorganic materials 0.000 description 7
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 7
- 230000006872 improvement Effects 0.000 description 7
- 230000035939 shock Effects 0.000 description 7
- 239000000243 solution Substances 0.000 description 7
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 6
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 6
- CPELXLSAUQHCOX-UHFFFAOYSA-N Hydrogen bromide Chemical compound Br CPELXLSAUQHCOX-UHFFFAOYSA-N 0.000 description 6
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- 239000003795 chemical substances by application Substances 0.000 description 6
- 229920001577 copolymer Polymers 0.000 description 6
- 238000004898 kneading Methods 0.000 description 6
- IOLCXVTUBQKXJR-UHFFFAOYSA-M potassium bromide Chemical compound [K+].[Br-] IOLCXVTUBQKXJR-UHFFFAOYSA-M 0.000 description 6
- 230000009467 reduction Effects 0.000 description 6
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 6
- 238000001228 spectrum Methods 0.000 description 6
- MNAHQWDCXOHBHK-UHFFFAOYSA-N 1-phenylpropane-1,1-diol Chemical compound CCC(O)(O)C1=CC=CC=C1 MNAHQWDCXOHBHK-UHFFFAOYSA-N 0.000 description 5
- KRHYYFGTRYWZRS-UHFFFAOYSA-N Fluorane Chemical compound F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 description 5
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 5
- 229920000122 acrylonitrile butadiene styrene Polymers 0.000 description 5
- 125000000217 alkyl group Chemical group 0.000 description 5
- 238000004458 analytical method Methods 0.000 description 5
- 238000013475 authorization Methods 0.000 description 5
- ZSTLPJLUQNQBDQ-UHFFFAOYSA-N azanylidyne(dihydroxy)-$l^{5}-phosphane Chemical compound OP(O)#N ZSTLPJLUQNQBDQ-UHFFFAOYSA-N 0.000 description 5
- 239000002585 base Substances 0.000 description 5
- 239000006227 byproduct Substances 0.000 description 5
- 238000011156 evaluation Methods 0.000 description 5
- 238000005227 gel permeation chromatography Methods 0.000 description 5
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 5
- 238000002156 mixing Methods 0.000 description 5
- 239000001301 oxygen Substances 0.000 description 5
- 229910052760 oxygen Inorganic materials 0.000 description 5
- 230000008569 process Effects 0.000 description 5
- 238000011160 research Methods 0.000 description 5
- 239000004215 Carbon black (E152) Substances 0.000 description 4
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 4
- 239000004793 Polystyrene Substances 0.000 description 4
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 4
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 4
- 230000002378 acidificating effect Effects 0.000 description 4
- 239000000654 additive Substances 0.000 description 4
- 239000003513 alkali Substances 0.000 description 4
- 125000003545 alkoxy group Chemical group 0.000 description 4
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 4
- 229910052731 fluorine Inorganic materials 0.000 description 4
- 239000011737 fluorine Substances 0.000 description 4
- 229910052736 halogen Inorganic materials 0.000 description 4
- 150000002367 halogens Chemical class 0.000 description 4
- FFUAGWLWBBFQJT-UHFFFAOYSA-N hexamethyldisilazane Chemical compound C[Si](C)(C)N[Si](C)(C)C FFUAGWLWBBFQJT-UHFFFAOYSA-N 0.000 description 4
- 229930195733 hydrocarbon Natural products 0.000 description 4
- 150000003014 phosphoric acid esters Chemical class 0.000 description 4
- 229920002223 polystyrene Polymers 0.000 description 4
- 229910052700 potassium Inorganic materials 0.000 description 4
- 239000011591 potassium Substances 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 4
- 238000000746 purification Methods 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- 238000004876 x-ray fluorescence Methods 0.000 description 4
- 238000005160 1H NMR spectroscopy Methods 0.000 description 3
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- 238000005133 29Si NMR spectroscopy Methods 0.000 description 3
- HXDOZKJGKXYMEW-UHFFFAOYSA-N 4-ethylphenol Chemical compound CCC1=CC=C(O)C=C1 HXDOZKJGKXYMEW-UHFFFAOYSA-N 0.000 description 3
- 239000005046 Chlorosilane Substances 0.000 description 3
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 3
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 229910019142 PO4 Inorganic materials 0.000 description 3
- 239000004721 Polyphenylene oxide Substances 0.000 description 3
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 3
- YSMRWXYRXBRSND-UHFFFAOYSA-N TOTP Chemical compound CC1=CC=CC=C1OP(=O)(OC=1C(=CC=CC=1)C)OC1=CC=CC=C1C YSMRWXYRXBRSND-UHFFFAOYSA-N 0.000 description 3
- 238000010521 absorption reaction Methods 0.000 description 3
- 230000000996 additive effect Effects 0.000 description 3
- 150000001340 alkali metals Chemical class 0.000 description 3
- 125000005250 alkyl acrylate group Chemical group 0.000 description 3
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 3
- 230000004888 barrier function Effects 0.000 description 3
- 125000005340 bisphosphate group Chemical group 0.000 description 3
- 238000011088 calibration curve Methods 0.000 description 3
- KOPOQZFJUQMUML-UHFFFAOYSA-N chlorosilane Chemical compound Cl[SiH3] KOPOQZFJUQMUML-UHFFFAOYSA-N 0.000 description 3
- 238000004891 communication Methods 0.000 description 3
- 238000006482 condensation reaction Methods 0.000 description 3
- 238000007334 copolymerization reaction Methods 0.000 description 3
- 229910000042 hydrogen bromide Inorganic materials 0.000 description 3
- 229910000040 hydrogen fluoride Inorganic materials 0.000 description 3
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 3
- 229910000043 hydrogen iodide Inorganic materials 0.000 description 3
- 230000007062 hydrolysis Effects 0.000 description 3
- 238000006460 hydrolysis reaction Methods 0.000 description 3
- 238000000465 moulding Methods 0.000 description 3
- 238000006386 neutralization reaction Methods 0.000 description 3
- 150000002825 nitriles Chemical class 0.000 description 3
- 150000001367 organochlorosilanes Chemical class 0.000 description 3
- 239000010452 phosphate Substances 0.000 description 3
- 238000006068 polycondensation reaction Methods 0.000 description 3
- 238000006116 polymerization reaction Methods 0.000 description 3
- 229920006380 polyphenylene oxide Polymers 0.000 description 3
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 3
- 229910052708 sodium Inorganic materials 0.000 description 3
- FVAUCKIRQBBSSJ-UHFFFAOYSA-M sodium iodide Chemical compound [Na+].[I-] FVAUCKIRQBBSSJ-UHFFFAOYSA-M 0.000 description 3
- 125000003011 styrenyl group Chemical group [H]\C(*)=C(/[H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 3
- 230000002195 synergetic effect Effects 0.000 description 3
- BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical group FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 0.000 description 3
- QPFMBZIOSGYJDE-UHFFFAOYSA-N 1,1,2,2-tetrachloroethane Chemical compound ClC(Cl)C(Cl)Cl QPFMBZIOSGYJDE-UHFFFAOYSA-N 0.000 description 2
- JLBJTVDPSNHSKJ-UHFFFAOYSA-N 4-Methylstyrene Chemical compound CC1=CC=C(C=C)C=C1 JLBJTVDPSNHSKJ-UHFFFAOYSA-N 0.000 description 2
- 125000004203 4-hydroxyphenyl group Chemical group [H]OC1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N Acrylic acid Chemical compound OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 2
- OIFBSDVPJOWBCH-UHFFFAOYSA-N Diethyl carbonate Chemical compound CCOC(=O)OCC OIFBSDVPJOWBCH-UHFFFAOYSA-N 0.000 description 2
- 239000007818 Grignard reagent Substances 0.000 description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 2
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 2
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 2
- 239000004594 Masterbatch (MB) Substances 0.000 description 2
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 2
- GYCMBHHDWRMZGG-UHFFFAOYSA-N Methylacrylonitrile Chemical compound CC(=C)C#N GYCMBHHDWRMZGG-UHFFFAOYSA-N 0.000 description 2
- 238000005481 NMR spectroscopy Methods 0.000 description 2
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
- YGYAWVDWMABLBF-UHFFFAOYSA-N Phosgene Chemical compound ClC(Cl)=O YGYAWVDWMABLBF-UHFFFAOYSA-N 0.000 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- YZCKVEUIGOORGS-NJFSPNSNSA-N Tritium Chemical compound [3H] YZCKVEUIGOORGS-NJFSPNSNSA-N 0.000 description 2
- 238000002441 X-ray diffraction Methods 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- 229920000800 acrylic rubber Polymers 0.000 description 2
- XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 description 2
- GHPGOEFPKIHBNM-UHFFFAOYSA-N antimony(3+);oxygen(2-) Chemical compound [O-2].[O-2].[O-2].[Sb+3].[Sb+3] GHPGOEFPKIHBNM-UHFFFAOYSA-N 0.000 description 2
- 238000001479 atomic absorption spectroscopy Methods 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 239000006085 branching agent Substances 0.000 description 2
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 229910052791 calcium Inorganic materials 0.000 description 2
- 238000004364 calculation method Methods 0.000 description 2
- YCIMNLLNPGFGHC-UHFFFAOYSA-N catechol Chemical compound OC1=CC=CC=C1O YCIMNLLNPGFGHC-UHFFFAOYSA-N 0.000 description 2
- DCFKHNIGBAHNSS-UHFFFAOYSA-N chloro(triethyl)silane Chemical compound CC[Si](Cl)(CC)CC DCFKHNIGBAHNSS-UHFFFAOYSA-N 0.000 description 2
- IJOOHPMOJXWVHK-UHFFFAOYSA-N chlorotrimethylsilane Chemical compound C[Si](C)(C)Cl IJOOHPMOJXWVHK-UHFFFAOYSA-N 0.000 description 2
- 238000009833 condensation Methods 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- BYLOHCRAPOSXLY-UHFFFAOYSA-N dichloro(diethyl)silane Chemical compound CC[Si](Cl)(Cl)CC BYLOHCRAPOSXLY-UHFFFAOYSA-N 0.000 description 2
- 239000003480 eluent Substances 0.000 description 2
- 229920006351 engineering plastic Polymers 0.000 description 2
- 150000002148 esters Chemical group 0.000 description 2
- CWAFVXWRGIEBPL-UHFFFAOYSA-N ethoxysilane Chemical compound CCO[SiH3] CWAFVXWRGIEBPL-UHFFFAOYSA-N 0.000 description 2
- 238000001879 gelation Methods 0.000 description 2
- 150000004795 grignard reagents Chemical class 0.000 description 2
- 230000010354 integration Effects 0.000 description 2
- 239000010422 internal standard material Substances 0.000 description 2
- 229910052744 lithium Inorganic materials 0.000 description 2
- AMXOYNBUYSYVKV-UHFFFAOYSA-M lithium bromide Chemical compound [Li+].[Br-] AMXOYNBUYSYVKV-UHFFFAOYSA-M 0.000 description 2
- KWGKDLIKAYFUFQ-UHFFFAOYSA-M lithium chloride Chemical compound [Li+].[Cl-] KWGKDLIKAYFUFQ-UHFFFAOYSA-M 0.000 description 2
- PQXKHYXIUOZZFA-UHFFFAOYSA-M lithium fluoride Chemical compound [Li+].[F-] PQXKHYXIUOZZFA-UHFFFAOYSA-M 0.000 description 2
- 229910052749 magnesium Inorganic materials 0.000 description 2
- VXWPONVCMVLXBW-UHFFFAOYSA-M magnesium;carbanide;iodide Chemical compound [CH3-].[Mg+2].[I-] VXWPONVCMVLXBW-UHFFFAOYSA-M 0.000 description 2
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 230000007246 mechanism Effects 0.000 description 2
- 239000000155 melt Substances 0.000 description 2
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
- 229920003986 novolac Polymers 0.000 description 2
- HMMGMWAXVFQUOA-UHFFFAOYSA-N octamethylcyclotetrasiloxane Chemical compound C[Si]1(C)O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)O1 HMMGMWAXVFQUOA-UHFFFAOYSA-N 0.000 description 2
- 125000000962 organic group Chemical group 0.000 description 2
- 239000008188 pellet Substances 0.000 description 2
- 239000012071 phase Substances 0.000 description 2
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 2
- 229920000058 polyacrylate Polymers 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- 229920001343 polytetrafluoroethylene Polymers 0.000 description 2
- 239000004810 polytetrafluoroethylene Substances 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 239000001294 propane Substances 0.000 description 2
- 229920003987 resole Polymers 0.000 description 2
- XUIMIQQOPSSXEZ-OUBTZVSYSA-N silicon-29 atom Chemical class [29Si] XUIMIQQOPSSXEZ-OUBTZVSYSA-N 0.000 description 2
- JVBXVOWTABLYPX-UHFFFAOYSA-L sodium dithionite Chemical compound [Na+].[Na+].[O-]S(=O)S([O-])=O JVBXVOWTABLYPX-UHFFFAOYSA-L 0.000 description 2
- PUZPDOWCWNUUKD-UHFFFAOYSA-M sodium fluoride Chemical compound [F-].[Na+] PUZPDOWCWNUUKD-UHFFFAOYSA-M 0.000 description 2
- 150000003440 styrenes Chemical class 0.000 description 2
- DHCDFWKWKRSZHF-UHFFFAOYSA-N sulfurothioic S-acid Chemical compound OS(O)(=O)=S DHCDFWKWKRSZHF-UHFFFAOYSA-N 0.000 description 2
- 238000001149 thermolysis Methods 0.000 description 2
- 125000003944 tolyl group Chemical group 0.000 description 2
- 229910052722 tritium Inorganic materials 0.000 description 2
- SHIYDRAMQRMTPZ-UHFFFAOYSA-N (3,5-dimethylphenyl) phenyl hydrogen phosphate Chemical compound C1(=CC=CC=C1)OP(OC1=CC(=CC(=C1)C)C)(O)=O SHIYDRAMQRMTPZ-UHFFFAOYSA-N 0.000 description 1
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- IWDCLRJOBJJRNH-UHFFFAOYSA-N p-cresol Chemical compound CC1=CC=C(O)C=C1 IWDCLRJOBJJRNH-UHFFFAOYSA-N 0.000 description 1
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 1
- QCDYQQDYXPDABM-UHFFFAOYSA-N phloroglucinol Chemical compound OC1=CC(O)=CC(O)=C1 QCDYQQDYXPDABM-UHFFFAOYSA-N 0.000 description 1
- 229960001553 phloroglucinol Drugs 0.000 description 1
- 150000003018 phosphorus compounds Chemical class 0.000 description 1
- 229910000073 phosphorus hydride Inorganic materials 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920001485 poly(butyl acrylate) polymer Polymers 0.000 description 1
- 229920001084 poly(chloroprene) Polymers 0.000 description 1
- 229920005672 polyolefin resin Polymers 0.000 description 1
- 229920005990 polystyrene resin Polymers 0.000 description 1
- LVTHXRLARFLXNR-UHFFFAOYSA-M potassium;1,1,2,2,3,3,4,4,4-nonafluorobutane-1-sulfonate Chemical compound [K+].[O-]S(=O)(=O)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F LVTHXRLARFLXNR-UHFFFAOYSA-M 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 238000002203 pretreatment Methods 0.000 description 1
- 239000005053 propyltrichlorosilane Substances 0.000 description 1
- 238000000197 pyrolysis Methods 0.000 description 1
- 238000006462 rearrangement reaction Methods 0.000 description 1
- 238000007363 ring formation reaction Methods 0.000 description 1
- 229910052701 rubidium Inorganic materials 0.000 description 1
- IGLNJRXAVVLDKE-UHFFFAOYSA-N rubidium atom Chemical compound [Rb] IGLNJRXAVVLDKE-UHFFFAOYSA-N 0.000 description 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 238000007086 side reaction Methods 0.000 description 1
- KCIKCCHXZMLVDE-UHFFFAOYSA-N silanediol Chemical compound O[SiH2]O KCIKCCHXZMLVDE-UHFFFAOYSA-N 0.000 description 1
- 125000005372 silanol group Chemical group 0.000 description 1
- 239000005049 silicon tetrachloride Substances 0.000 description 1
- 229910001388 sodium aluminate Inorganic materials 0.000 description 1
- HRZFUMHJMZEROT-UHFFFAOYSA-L sodium disulfite Chemical compound [Na+].[Na+].[O-]S(=O)S([O-])(=O)=O HRZFUMHJMZEROT-UHFFFAOYSA-L 0.000 description 1
- 239000007790 solid phase Substances 0.000 description 1
- 238000000638 solvent extraction Methods 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 229910052712 strontium Inorganic materials 0.000 description 1
- CIOAGBVUUVVLOB-UHFFFAOYSA-N strontium atom Chemical compound [Sr] CIOAGBVUUVVLOB-UHFFFAOYSA-N 0.000 description 1
- 239000011115 styrene butadiene Substances 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- 150000003871 sulfonates Chemical class 0.000 description 1
- 238000010557 suspension polymerization reaction Methods 0.000 description 1
- 230000002194 synthesizing effect Effects 0.000 description 1
- 229920003051 synthetic elastomer Polymers 0.000 description 1
- 229920001897 terpolymer Polymers 0.000 description 1
- 125000001973 tert-pentyl group Chemical group [H]C([H])([H])C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- ZQZCOBSUOFHDEE-UHFFFAOYSA-N tetrapropyl silicate Chemical compound CCCO[Si](OCCC)(OCCC)OCCC ZQZCOBSUOFHDEE-UHFFFAOYSA-N 0.000 description 1
- 229920005992 thermoplastic resin Polymers 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 238000005809 transesterification reaction Methods 0.000 description 1
- STCOOQWBFONSKY-UHFFFAOYSA-N tributyl phosphate Chemical compound CCCCOP(=O)(OCCCC)OCCCC STCOOQWBFONSKY-UHFFFAOYSA-N 0.000 description 1
- GPHYWIXZJBGHPO-UHFFFAOYSA-N trichloro(6-methylheptyl)silane Chemical compound CC(C)CCCCC[Si](Cl)(Cl)Cl GPHYWIXZJBGHPO-UHFFFAOYSA-N 0.000 description 1
- GQIUQDDJKHLHTB-UHFFFAOYSA-N trichloro(ethenyl)silane Chemical compound Cl[Si](Cl)(Cl)C=C GQIUQDDJKHLHTB-UHFFFAOYSA-N 0.000 description 1
- ZOYFEXPFPVDYIS-UHFFFAOYSA-N trichloro(ethyl)silane Chemical compound CC[Si](Cl)(Cl)Cl ZOYFEXPFPVDYIS-UHFFFAOYSA-N 0.000 description 1
- DOEHJNBEOVLHGL-UHFFFAOYSA-N trichloro(propyl)silane Chemical compound CCC[Si](Cl)(Cl)Cl DOEHJNBEOVLHGL-UHFFFAOYSA-N 0.000 description 1
- HXOGQBSDPSMHJK-UHFFFAOYSA-N triethoxy(6-methylheptyl)silane Chemical compound CCO[Si](OCC)(OCC)CCCCCC(C)C HXOGQBSDPSMHJK-UHFFFAOYSA-N 0.000 description 1
- DENFJSAFJTVPJR-UHFFFAOYSA-N triethoxy(ethyl)silane Chemical compound CCO[Si](CC)(OCC)OCC DENFJSAFJTVPJR-UHFFFAOYSA-N 0.000 description 1
- JCVQKRGIASEUKR-UHFFFAOYSA-N triethoxy(phenyl)silane Chemical compound CCO[Si](OCC)(OCC)C1=CC=CC=C1 JCVQKRGIASEUKR-UHFFFAOYSA-N 0.000 description 1
- NBXZNTLFQLUFES-UHFFFAOYSA-N triethoxy(propyl)silane Chemical compound CCC[Si](OCC)(OCC)OCC NBXZNTLFQLUFES-UHFFFAOYSA-N 0.000 description 1
- DQWPFSLDHJDLRL-UHFFFAOYSA-N triethyl phosphate Chemical compound CCOP(=O)(OCC)OCC DQWPFSLDHJDLRL-UHFFFAOYSA-N 0.000 description 1
- XPDWGBQVDMORPB-UHFFFAOYSA-N trifluoromethane acid Natural products FC(F)F XPDWGBQVDMORPB-UHFFFAOYSA-N 0.000 description 1
- HQYALQRYBUJWDH-UHFFFAOYSA-N trimethoxy(propyl)silane Chemical compound CCC[Si](OC)(OC)OC HQYALQRYBUJWDH-UHFFFAOYSA-N 0.000 description 1
- CYTQBVOFDCPGCX-UHFFFAOYSA-N trimethyl phosphite Chemical compound COP(OC)OC CYTQBVOFDCPGCX-UHFFFAOYSA-N 0.000 description 1
- 239000005051 trimethylchlorosilane Substances 0.000 description 1
- XZZNDPSIHUTMOC-UHFFFAOYSA-N triphenyl phosphate Chemical compound C=1C=CC=CC=1OP(OC=1C=CC=CC=1)(=O)OC1=CC=CC=C1 XZZNDPSIHUTMOC-UHFFFAOYSA-N 0.000 description 1
- BIKXLKXABVUSMH-UHFFFAOYSA-N trizinc;diborate Chemical compound [Zn+2].[Zn+2].[Zn+2].[O-]B([O-])[O-].[O-]B([O-])[O-] BIKXLKXABVUSMH-UHFFFAOYSA-N 0.000 description 1
- 239000005050 vinyl trichlorosilane Substances 0.000 description 1
- 125000005023 xylyl group Chemical group 0.000 description 1
- 150000003751 zinc Chemical class 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
Classifications
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L25/00—Compositions of, homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an aromatic carbocyclic ring; Compositions of derivatives of such polymers
- C08L25/02—Homopolymers or copolymers of hydrocarbons
- C08L25/04—Homopolymers or copolymers of styrene
- C08L25/08—Copolymers of styrene
-
- 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
Abstract
Description
有机基聚硅氧烷(B) | 重均分子量 | 端基相对含量 | 无机金属盐含量(wt%) | |||
No. | 结构和成分* | OEt(wt%) | OH(wt%) | |||
S-1 | MQ | (Me3SiO0.5)0.4(SiO2)0.6 | 9,400 | 3.2 | 0.7 | 未测出 |
S-2 | DT | (PhMeSiO)0.2(PhSiO1.5)0.52(MeSiO1.5)0.28 | 2,500 | 0.3 | 2.8 | 未测出 |
S-3 | T | (PhSiO1.5)0.33(n-PrSiO1.5)0.67 | 3,760 | <0.5 | 3.0 | 未测出 |
S-4 | MT | (PhSiO1.5)0.53(n-PrSiO1.5)0.26(Me3SiO0.5)0.21 | 2,500 | <0.5 | <0.1 | 未测出 |
S-5 | MD | Me3SiO(PhMeSiO)nSiMe3 | 1,640 | 0 | 0 | 未测出 |
S-6 | DTQ | (PhMeSiO)0.2(PhSiO1.5)0.6(SiO2)0.2 | 2,300 | 16.0 | <0.1 | 0.102(NaCl) |
S-7 | DTQ | (PhMeSiO)0.2(PhSiO1.5)0.6(SiO2)0.2 | 970 | 18.9 | 0.92 | 未测出 |
S-8 | MTQ | (Me3SiO0.5)0.38(PhSiO1.5)0.05(SiO2)0.57 | 8,800 | 4.0 | 0.3 | 0.203(NaCl) |
S-9 | MTQ | (Me3SiO0.5)0.35(PhSiO1.5)0.13(SiO2)0.52 | 7,440 | 5.3 | 0.4 | 0.001(NaCl) |
S-10 | MTQ | (Me3SiO0.5)0.35(n-PrSiO1.5)0.13(SiO2)0.52 | 8,540 | 7.1 | <0.1 | 0.153(NaCl) |
S-11 | MTQ | (Me3SiO0.5)0.35(n-PrSiO1.5)0.13(SiO2)0.52 | 8,880 | 6.6 | 0.4 | 0.004(NaCl) |
S-12 | MTQ | (Me3SiO0.5)0.35(iso-OctSiO1.5)0.13(SiO2)0.52 | 10,100 | 4.3 | 0.4 | 0.124(NaCl) |
S-13 | MTQ | (Me3SiO0.5)0.35(iso-OctSiO1.5)0.13(SiO2)0.52 | 10,100 | 4.3 | 0.4 | 0.003(NaCl) |
S-14 | MDQ | (Me3SiO0.5)0.31(Me2SiO)0.21(SiO2)0.48 | 15,600 | 2.5 | 0.2 | 0.073(NaCl) |
S-15 | MQ | (Me3SiO0.5)0.35(SiO2)0.65 | 115,000 | 4.6 | 0.2 | 0.142(NaCl) |
S-16 | MT | (Me3SiO)3SiPh | 372 | 0 | 0 | 未测出 |
配方(重量份数) | UL-94分析 | ||||||||
树脂成分(A) | 有机基聚硅氧烷(B) | 无机金属盐(C) | 平均熄火时间(秒) | 最大熄火时间(秒) | 滴落数 | 评估 | |||
PC | AS | ABS | |||||||
例1 | 80 | 10 | 10 | 11.1(S-1) | 0.009(NaCl) | 11.2 | 25 | 0/10 | V-1 |
例2 | 80 | 10 | 10 | 11.1(S-1) | 0.018(NaCl) | 7.3 | 14 | 0/10 | V-1 |
例3 | 80 | 10 | 10 | 11.1(S-1) | 0.073(NaCl) | 8.2 | 19 | 0/10 | V-1 |
例4 | 80 | 10 | 10 | 11.1(S-1) | 0.023(KCl) | 9.0 | 16 | 0/10 | V-1 |
例5 | 80 | 10 | 10 | 11.1(S-1) | 0.032(NaBr) | 10.8 | 24 | 0/10 | V-1 |
例6 | 80 | 10 | 10 | 11.1(S-1) | 0.027(NoNO3) | 11.5 | 23 | 0/10 | V-1 |
对比例1 | 80 | 10 | 10 | 0 | 0 | 30.4 | 41 | 10/10 | 标准以外 |
对比例2 | 80 | 10 | 10 | 11.1(S-1) | 0 | 32.3 | 76 | 2/10 | 标准以外 |
对比例3 | 80 | 10 | 10 | 0 | 0.05(F114P)* | 44.5 | 87 | 10/10 | 标准以外 |
对比例4 | 80 | 10 | 10 | 0 | 0.017(NaCl) | 37.8 | 90 | 10/10 | 标准以外 |
对比例5 | 80 | 10 | 10 | 11.1(S-1) | 0.05(F114P)* | 45.9 | 141 | 8/10 | 标准以外 |
对比例6 | 80 | 10 | 10 | 11.1(S-1) | 0.2(F114P)* | 59.2 | 152 | 10/10 | 标准以外 |
对比例7 | 80 | 10 | 10 | 11.1(S-1) | 1.0(F114P)* | 5件样品中有3件燃烧至全部燃尽 | |||
对比例8 | 80 | 10 | 10 | 11.1(S-1) | 0.05(KSS)* | 39.2 | 136 | 10/10 | 标准以外 |
配方(重量份数) | UL-94分析 | ||||||||
树脂成分(A) | 有机基聚硅氧烷(B) | 无机金属盐(C) | 平均熄火时间(秒) | 最大熄火时间(秒) | 滴落数 | 评估 | |||
PC | AS | ABS | |||||||
例7 | 80 | 10 | 10 | 11.1(S-2) | 0.018(NaCl) | 8.8 | 18 | 0/10 | V-1 |
例8 | 80 | 10 | 10 | 11.1(S-2) | 0.035(CaCl2) | 9.0 | 15 | 0/10 | V-1 |
例9 | 80 | 10 | 10 | 11.1(S-3) | 0.037(NaCl) | 5.1 | 11 | 0/10 | V-1 |
例10 | 80 | 10 | 10 | 11.1(S-4) | 0.018(NaCl) | 4.3 | 9 | 0/10 | V-0 |
例11 | 80 | 10 | 10 | 11.1(S-5) | 0.018(NaCl) | 5.8 | 12 | 0/10 | V-1 |
对比例9 | 80 | 10 | 10 | 11.1(S-2) | 0 | 20.3 | 95 | 2/10 | 标准以外 |
对比例10 | 80 | 10 | 10 | 11.1(S-3) | 0 | 17.3 | 76 | 5/10 | 标准以外 |
对比例11 | 80 | 10 | 10 | 11.1(S-4) | 0 | 15.4 | 66 | 2/10 | 标准以外 |
对比例12 | 80 | 10 | 10 | 11.1(S-5) | 0 | 8.5 | 19 | 2/10 | 标准以外 |
配方(重量份数) | UL-94分析 | ||||||||
树脂成分(A) | 有机基聚硅氧烷(B) | 无机金属盐*1(C) | 平均熄火时间(秒) | 最大熄火时间(秒) | 滴落数 | 评估 | |||
PC | AS | ABS | |||||||
例12 | 80 | 10 | 10 | 11.1(S-6) | 0.011(NaCl) | 7.2 | 13 | 0/10 | V-1 |
对比例13 | 80 | 10 | 10 | 11.1(S-7) | 0 | 35.5 | 101 | 4/10 | 标准以外 |
例13 | 80 | 10 | 10 | 5.3(S-8) | 0.011(NaCl) | 4.6 | 7 | 0/10 | V-0 |
对比例14 | 80 | 10 | 10 | 11.1(S-9) | 0.0001(NaCl) | 10.8 | 24 | 4/10 | 标准以外 |
例14 | 80 | 10 | 10 | 11.1(S-10) | 0.017(NaCl) | 5.0 | 7 | 0/10 | V-0 |
对比例15 | 80 | 10 | 10 | 11.1(S-11) | 0.0004(NaCl) | 25.8 | 103 | 0/10 | 标准以外 |
例15 | 80 | 10 | 10 | 11.1(S-12) | 0.014(NaCl) | 4.9 | 8 | 0/10 | V-0 |
对比例16 | 80 | 10 | 10 | 11.1(S-13) | 0.0003(NaCl) | 42.0 | 104 | 0/10 | 标准以外 |
例16 | 80 | 10 | 10 | 11.1(S-14) | 0.008(NaCl) | 7.7 | 19 | 0/10 | V-1 |
对比例17 | 80 | 10 | 10 | 11.1(S-15) | 0.016(NaCl) | 17.5 | 91 | 4/10 | 标准以外 |
对比例18 | 80 | 10 | 10 | 11.1(S-16) | 0.018(NaCl)*2 | 22.6 | 57 | 3/10 | 标准以外 |
Claims (4)
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JP2001313442A JP3865295B2 (ja) | 2001-10-11 | 2001-10-11 | 難燃性樹脂組成物 |
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CN1197913C true CN1197913C (zh) | 2005-04-20 |
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US (1) | US6825264B2 (zh) |
EP (1) | EP1302510B1 (zh) |
JP (1) | JP3865295B2 (zh) |
CN (1) | CN1197913C (zh) |
DE (1) | DE60213735T2 (zh) |
PL (1) | PL206130B1 (zh) |
SG (1) | SG143016A1 (zh) |
TW (1) | TWI297347B (zh) |
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US7731881B2 (en) * | 2003-12-30 | 2010-06-08 | Sabic Innovative Plastics Ip B.V. | Method for making fog resistant thermoplastic articles and articles made therefrom |
US7220792B2 (en) * | 2003-12-30 | 2007-05-22 | General Electric Company | Water resistant permanent antistatic thermoplastic composition |
US8604151B2 (en) | 2004-02-02 | 2013-12-10 | Dow Corning Corporation | Bodied siloxane resin including M, Q, and T-propyl units and capped with additional M units |
EP1711551B1 (en) * | 2004-02-02 | 2007-08-29 | Dow Corning Corporation | Mq-t propyl siloxane resins |
JP4678338B2 (ja) * | 2006-06-06 | 2011-04-27 | 信越化学工業株式会社 | 有機樹脂難燃化用添加剤、難燃性樹脂組成物及びその成形品 |
CN101104730B (zh) * | 2006-07-14 | 2012-09-05 | 上海普利特复合材料有限公司 | 一种低氟含量的阻燃聚碳酸酯/苯乙烯基树脂组合物 |
JP2008266362A (ja) * | 2007-04-16 | 2008-11-06 | Mitsubishi Engineering Plastics Corp | 難燃性芳香族ポリカーボネート樹脂組成物及び樹脂成形体 |
WO2009067232A1 (en) * | 2007-11-20 | 2009-05-28 | Dow Corning Corporation | Article comprising fibers and a method of forming the same |
CN102083409B (zh) * | 2008-07-30 | 2014-04-16 | 陶氏康宁公司 | 具有改进的相容性并提供改进的防晒效果的个人护理组合物 |
CN101747609B (zh) * | 2008-12-22 | 2013-06-19 | 广州熵能聚合物技术有限公司 | 阻燃性聚碳酸酯组合物 |
CN102604246A (zh) * | 2012-03-19 | 2012-07-25 | 上海锦湖日丽塑料有限公司 | 高效阻燃的苯乙烯类树脂组合物 |
EP3085715A1 (en) * | 2012-10-31 | 2016-10-26 | Mitsubishi Rayon Co., Ltd. | Polyorganosiloxane-containing graft copolymer, resin composition, and molded article |
EP3092264B1 (en) | 2014-01-08 | 2019-10-23 | Dow Silicones Corporation | Method for capping mq-type silicone resins |
CN104804390B (zh) * | 2015-04-09 | 2017-05-10 | 深圳市丹华塑胶科技有限公司 | 共混复合超韧pc耐候耐腐蚀材料及其在移动互联的应用 |
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JP3163596B2 (ja) * | 1994-12-22 | 2001-05-08 | 出光石油化学株式会社 | 難燃性ポリカーボネート樹脂組成物 |
JP3151789B2 (ja) * | 1994-12-22 | 2001-04-03 | 出光石油化学株式会社 | 難燃性ポリカーボネート樹脂組成物 |
US6001921A (en) * | 1997-09-11 | 1999-12-14 | Nec Corporation | Flame retardant resin composition |
JP3835497B2 (ja) * | 1997-11-05 | 2006-10-18 | 日本電気株式会社 | 難燃性ポリカーボネート樹脂組成物 |
DE69833246T2 (de) * | 1997-11-19 | 2006-10-05 | Shin-Etsu Chemical Co., Ltd. | Flammwidrige Kunststoffmischungen |
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US6454969B1 (en) | 1998-02-05 | 2002-09-24 | Asahi Kasei Kabushiki Kaisha | Silicon-containing flame retardant |
JP3767669B2 (ja) * | 1998-11-17 | 2006-04-19 | 信越化学工業株式会社 | 難燃性樹脂組成物 |
DE10080144T1 (de) | 1999-02-08 | 2001-03-22 | Asahi Chemical Ind | Aromatische Polycarbonatharz-Zusammensetzung |
JP4368977B2 (ja) * | 1999-07-28 | 2009-11-18 | 出光興産株式会社 | ポリカーボネート樹脂組成物 |
WO2001038438A2 (en) * | 1999-11-26 | 2001-05-31 | General Electric Company | Flame-retardant resin composition and molded article consisting of the same |
JP4322376B2 (ja) * | 1999-11-26 | 2009-08-26 | Sabicイノベーティブプラスチックスジャパン合同会社 | 難燃性樹脂組成物およびその成型品 |
JP3439710B2 (ja) * | 2000-01-20 | 2003-08-25 | 東レ・ダウコーニング・シリコーン株式会社 | 難燃性有機樹脂組成物 |
DE60108825T2 (de) * | 2000-03-28 | 2006-01-19 | Teijin Chemicals Ltd. | Regenerierte harzzusammensetzung |
JP3833056B2 (ja) * | 2000-08-07 | 2006-10-11 | 旭化成ケミカルズ株式会社 | 難燃性芳香族ポリカーボネート樹脂組成物 |
-
2001
- 2001-10-11 JP JP2001313442A patent/JP3865295B2/ja not_active Expired - Fee Related
-
2002
- 2002-10-07 TW TW091123128A patent/TWI297347B/zh not_active IP Right Cessation
- 2002-10-08 DE DE60213735T patent/DE60213735T2/de not_active Expired - Lifetime
- 2002-10-08 EP EP02256943A patent/EP1302510B1/en not_active Expired - Lifetime
- 2002-10-09 SG SG200206164-6A patent/SG143016A1/en unknown
- 2002-10-10 PL PL356575A patent/PL206130B1/pl unknown
- 2002-10-11 US US10/268,983 patent/US6825264B2/en not_active Expired - Fee Related
- 2002-10-11 CN CN02130858.6A patent/CN1197913C/zh not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
PL356575A1 (en) | 2003-04-22 |
EP1302510B1 (en) | 2006-08-09 |
SG143016A1 (en) | 2008-06-27 |
TWI297347B (en) | 2008-06-01 |
DE60213735D1 (de) | 2006-09-21 |
DE60213735T2 (de) | 2007-08-23 |
PL206130B1 (pl) | 2010-07-30 |
JP2003119368A (ja) | 2003-04-23 |
JP3865295B2 (ja) | 2007-01-10 |
EP1302510A1 (en) | 2003-04-16 |
US20030109660A1 (en) | 2003-06-12 |
CN1412246A (zh) | 2003-04-23 |
US6825264B2 (en) | 2004-11-30 |
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