CN105348534A - 一种纳米二氧化硅杂化乙烯基苯基硅中物、其制备方法及应用 - Google Patents
一种纳米二氧化硅杂化乙烯基苯基硅中物、其制备方法及应用 Download PDFInfo
- Publication number
- CN105348534A CN105348534A CN201510854357.0A CN201510854357A CN105348534A CN 105348534 A CN105348534 A CN 105348534A CN 201510854357 A CN201510854357 A CN 201510854357A CN 105348534 A CN105348534 A CN 105348534A
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- China
- Prior art keywords
- silicon dioxide
- thing
- ethenylphenyl
- nano silicon
- dioxide hybridization
- 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.)
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- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 title claims abstract description 190
- 235000012239 silicon dioxide Nutrition 0.000 title claims abstract description 95
- 238000000034 method Methods 0.000 title claims abstract description 49
- 239000000377 silicon dioxide Substances 0.000 title claims abstract description 11
- 239000000463 material Substances 0.000 title abstract description 10
- MJULMZZKFYNTHK-UHFFFAOYSA-N ethenyl(phenyl)silicon Chemical compound C=C[Si]C1=CC=CC=C1 MJULMZZKFYNTHK-UHFFFAOYSA-N 0.000 title abstract 4
- 238000006243 chemical reaction Methods 0.000 claims abstract description 40
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims abstract description 24
- 229920002554 vinyl polymer Polymers 0.000 claims abstract description 23
- 239000002245 particle Substances 0.000 claims abstract description 6
- 239000005543 nano-size silicon particle Substances 0.000 claims description 88
- 229910052710 silicon Inorganic materials 0.000 claims description 88
- 239000010703 silicon Substances 0.000 claims description 88
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims description 87
- 238000009396 hybridization Methods 0.000 claims description 84
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 40
- 239000011259 mixed solution Substances 0.000 claims description 33
- 238000003756 stirring Methods 0.000 claims description 33
- 238000010792 warming Methods 0.000 claims description 32
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 26
- 239000003960 organic solvent Substances 0.000 claims description 26
- 238000004821 distillation Methods 0.000 claims description 22
- 230000007613 environmental effect Effects 0.000 claims description 18
- 238000002360 preparation method Methods 0.000 claims description 18
- 239000000243 solution Substances 0.000 claims description 17
- BOTDANWDWHJENH-UHFFFAOYSA-N Tetraethyl orthosilicate Chemical compound CCO[Si](OCC)(OCC)OCC BOTDANWDWHJENH-UHFFFAOYSA-N 0.000 claims description 14
- 229920005989 resin Polymers 0.000 claims description 14
- 239000011347 resin Substances 0.000 claims description 14
- 229910052757 nitrogen Inorganic materials 0.000 claims description 13
- 239000000203 mixture Substances 0.000 claims description 12
- 239000007787 solid Substances 0.000 claims description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 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 9
- DTQVDTLACAAQTR-UHFFFAOYSA-N Trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-N 0.000 claims description 8
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 7
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 6
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims description 6
- 239000002994 raw material Substances 0.000 claims description 6
- 101100152731 Arabidopsis thaliana TH2 gene Proteins 0.000 claims description 4
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 claims description 4
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 claims description 4
- 239000007864 aqueous solution Substances 0.000 claims description 4
- 238000011049 filling Methods 0.000 claims description 3
- GSNUFIFRDBKVIE-UHFFFAOYSA-N DMF Natural products CC1=CC=C(C)O1 GSNUFIFRDBKVIE-UHFFFAOYSA-N 0.000 claims description 2
- 239000003795 chemical substances by application Substances 0.000 claims description 2
- BITPLIXHRASDQB-UHFFFAOYSA-N ethenyl-[ethenyl(dimethyl)silyl]oxy-dimethylsilane Chemical group C=C[Si](C)(C)O[Si](C)(C)C=C BITPLIXHRASDQB-UHFFFAOYSA-N 0.000 claims description 2
- 239000000565 sealant Substances 0.000 claims description 2
- 238000004513 sizing Methods 0.000 claims description 2
- 239000004593 Epoxy Substances 0.000 abstract description 11
- 239000003973 paint Substances 0.000 abstract description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract description 2
- 239000003054 catalyst Substances 0.000 abstract description 2
- 239000007789 gas Substances 0.000 abstract description 2
- 239000001257 hydrogen Substances 0.000 abstract description 2
- 229910052739 hydrogen Inorganic materials 0.000 abstract description 2
- 229920003055 poly(ester-imide) Polymers 0.000 abstract description 2
- 229920000728 polyester Polymers 0.000 abstract description 2
- 239000003607 modifier Substances 0.000 abstract 1
- 229920001296 polysiloxane Polymers 0.000 abstract 1
- 230000000052 comparative effect Effects 0.000 description 18
- 230000009970 fire resistant effect Effects 0.000 description 15
- -1 isopropyl ester Chemical class 0.000 description 10
- 239000002253 acid Substances 0.000 description 9
- 238000001816 cooling Methods 0.000 description 9
- 239000003999 initiator Substances 0.000 description 9
- 239000003381 stabilizer Substances 0.000 description 9
- 238000003860 storage Methods 0.000 description 9
- 239000008367 deionised water Substances 0.000 description 6
- 229910021641 deionized water Inorganic materials 0.000 description 6
- 238000012986 modification Methods 0.000 description 5
- 230000004048 modification Effects 0.000 description 5
- 238000005227 gel permeation chromatography Methods 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 3
- 239000003822 epoxy resin Substances 0.000 description 3
- 229920000647 polyepoxide Polymers 0.000 description 3
- 238000006116 polymerization reaction Methods 0.000 description 3
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical group COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 2
- BGNXCDMCOKJUMV-UHFFFAOYSA-N Tert-Butylhydroquinone Chemical compound CC(C)(C)C1=CC(O)=CC=C1O BGNXCDMCOKJUMV-UHFFFAOYSA-N 0.000 description 2
- DAKWPKUUDNSNPN-UHFFFAOYSA-N Trimethylolpropane triacrylate Chemical compound C=CC(=O)OCC(CC)(COC(=O)C=C)COC(=O)C=C DAKWPKUUDNSNPN-UHFFFAOYSA-N 0.000 description 2
- 235000019400 benzoyl peroxide Nutrition 0.000 description 2
- 238000011065 in-situ storage Methods 0.000 description 2
- 238000009413 insulation Methods 0.000 description 2
- 239000002114 nanocomposite Substances 0.000 description 2
- 239000002105 nanoparticle Substances 0.000 description 2
- NWVVVBRKAWDGAB-UHFFFAOYSA-N p-methoxyphenol Chemical compound COC1=CC=C(O)C=C1 NWVVVBRKAWDGAB-UHFFFAOYSA-N 0.000 description 2
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinyl group Chemical group C1(O)=CC(O)=CC=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 2
- JZODKRWQWUWGCD-UHFFFAOYSA-N 2,5-di-tert-butylbenzene-1,4-diol Chemical group CC(C)(C)C1=CC(O)=C(C(C)(C)C)C=C1O JZODKRWQWUWGCD-UHFFFAOYSA-N 0.000 description 1
- XMNIXWIUMCBBBL-UHFFFAOYSA-N 2-(2-phenylpropan-2-ylperoxy)propan-2-ylbenzene Chemical compound C=1C=CC=CC=1C(C)(C)OOC(C)(C)C1=CC=CC=C1 XMNIXWIUMCBBBL-UHFFFAOYSA-N 0.000 description 1
- LJRSZGKUUZPHEB-UHFFFAOYSA-N 2-[2-(2-prop-2-enoyloxypropoxy)propoxy]propyl prop-2-enoate Chemical group C=CC(=O)OC(C)COC(C)COC(C)COC(=O)C=C LJRSZGKUUZPHEB-UHFFFAOYSA-N 0.000 description 1
- FUOZJYASZOSONT-UHFFFAOYSA-N 2-propan-2-yl-1h-imidazole Chemical compound CC(C)C1=NC=CN1 FUOZJYASZOSONT-UHFFFAOYSA-N 0.000 description 1
- 239000004925 Acrylic resin Substances 0.000 description 1
- 229920000178 Acrylic resin Polymers 0.000 description 1
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 1
- 0 CC(C)(C(C#N)OC)[Si](*)(*)*(I)=C Chemical compound CC(C)(C(C#N)OC)[Si](*)(*)*(I)=C 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- RPSIYHXLSWPDLN-UHFFFAOYSA-N [Ti].[O].C(C)C(=O)C(=O)C Chemical group [Ti].[O].C(C)C(=O)C(=O)C RPSIYHXLSWPDLN-UHFFFAOYSA-N 0.000 description 1
- 238000007171 acid catalysis Methods 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- QABCGOSYZHCPGN-UHFFFAOYSA-N chloro(dimethyl)silicon Chemical compound C[Si](C)Cl QABCGOSYZHCPGN-UHFFFAOYSA-N 0.000 description 1
- YQHLDYVWEZKEOX-UHFFFAOYSA-N cumene hydroperoxide Chemical compound OOC(C)(C)C1=CC=CC=C1 YQHLDYVWEZKEOX-UHFFFAOYSA-N 0.000 description 1
- OSXYHAQZDCICNX-UHFFFAOYSA-N dichloro(diphenyl)silane Chemical compound C=1C=CC=CC=1[Si](Cl)(Cl)C1=CC=CC=C1 OSXYHAQZDCICNX-UHFFFAOYSA-N 0.000 description 1
- LIKFHECYJZWXFJ-UHFFFAOYSA-N dimethyldichlorosilane Chemical compound C[Si](C)(Cl)Cl LIKFHECYJZWXFJ-UHFFFAOYSA-N 0.000 description 1
- KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical class [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- ARLJCLKHRZGWGL-UHFFFAOYSA-N ethenylsilicon Chemical compound [Si]C=C ARLJCLKHRZGWGL-UHFFFAOYSA-N 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000009998 heat setting Methods 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Chemical compound OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 description 1
- 238000004452 microanalysis Methods 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 238000011056 performance test Methods 0.000 description 1
- 239000002861 polymer material Substances 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 238000004062 sedimentation Methods 0.000 description 1
- 239000012703 sol-gel precursor Substances 0.000 description 1
- 238000003980 solgel method Methods 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 238000010189 synthetic method Methods 0.000 description 1
- 239000004250 tert-Butylhydroquinone Substances 0.000 description 1
- 235000019281 tert-butylhydroquinone Nutrition 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 238000012360 testing method Methods 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
- 229920006337 unsaturated polyester resin Polymers 0.000 description 1
- 239000002966 varnish Substances 0.000 description 1
- 239000005050 vinyl trichlorosilane Substances 0.000 description 1
Classifications
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
- Y02A50/00—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
- Y02A50/20—Air quality improvement or preservation, e.g. vehicle emission control or emission reduction by using catalytic converters
Landscapes
- Silicon Polymers (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
Description
Claims (10)
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
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CN201510854357.0A CN105348534B (zh) | 2015-11-30 | 2015-11-30 | 一种纳米二氧化硅杂化乙烯基苯基硅中物、其制备方法及应用 |
PCT/CN2016/096258 WO2017092412A1 (zh) | 2015-11-30 | 2016-08-22 | 一种纳米二氧化硅杂化乙烯基苯基硅中物、其制备方法及在环保绝缘漆中的应用 |
US15/992,176 US10662291B2 (en) | 2015-11-30 | 2018-05-30 | Nano-silica hybrid vinyl phenyl silicon intermediate, preparation method thereof and use thereof in environmentally-friendly insulating varnish |
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CN201510854357.0A CN105348534B (zh) | 2015-11-30 | 2015-11-30 | 一种纳米二氧化硅杂化乙烯基苯基硅中物、其制备方法及应用 |
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CN105348534A true CN105348534A (zh) | 2016-02-24 |
CN105348534B CN105348534B (zh) | 2017-02-08 |
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Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN106279331A (zh) * | 2016-07-27 | 2017-01-04 | 宋火良 | 胆酸类肝病治疗药物 |
WO2017092412A1 (zh) * | 2015-11-30 | 2017-06-08 | 苏州太湖电工新材料股份有限公司 | 一种纳米二氧化硅杂化乙烯基苯基硅中物、其制备方法及在环保绝缘漆中的应用 |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1235170A (zh) * | 1998-05-09 | 1999-11-17 | 中国科学院长春应用化学研究所 | 乙烯基有机/无机纳米杂化材料的合成方法 |
US20020091220A1 (en) * | 2000-10-12 | 2002-07-11 | Tsuneo Kimura | Room temperature curable organopolysiloxane compositions |
CN102030906A (zh) * | 2010-11-16 | 2011-04-27 | 北方涂料工业研究设计院 | 一种耐高温重防腐涂料用有机-无机杂化树脂的制备 |
CN103145992A (zh) * | 2013-03-20 | 2013-06-12 | 苏州太湖电工新材料股份有限公司 | 一种乙烯基硅中物,其制备方法及在制备耐高温电机无溶剂绝缘漆中的应用 |
CN104220532A (zh) * | 2012-04-11 | 2014-12-17 | 日东电工株式会社 | 阻燃性硅树脂组合物和阻燃性硅树脂片 |
-
2015
- 2015-11-30 CN CN201510854357.0A patent/CN105348534B/zh active Active
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1235170A (zh) * | 1998-05-09 | 1999-11-17 | 中国科学院长春应用化学研究所 | 乙烯基有机/无机纳米杂化材料的合成方法 |
US20020091220A1 (en) * | 2000-10-12 | 2002-07-11 | Tsuneo Kimura | Room temperature curable organopolysiloxane compositions |
CN102030906A (zh) * | 2010-11-16 | 2011-04-27 | 北方涂料工业研究设计院 | 一种耐高温重防腐涂料用有机-无机杂化树脂的制备 |
CN104220532A (zh) * | 2012-04-11 | 2014-12-17 | 日东电工株式会社 | 阻燃性硅树脂组合物和阻燃性硅树脂片 |
CN103145992A (zh) * | 2013-03-20 | 2013-06-12 | 苏州太湖电工新材料股份有限公司 | 一种乙烯基硅中物,其制备方法及在制备耐高温电机无溶剂绝缘漆中的应用 |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2017092412A1 (zh) * | 2015-11-30 | 2017-06-08 | 苏州太湖电工新材料股份有限公司 | 一种纳米二氧化硅杂化乙烯基苯基硅中物、其制备方法及在环保绝缘漆中的应用 |
US10662291B2 (en) | 2015-11-30 | 2020-05-26 | Suzhou Taihu Electric Advanced Material Co, Ltd. | Nano-silica hybrid vinyl phenyl silicon intermediate, preparation method thereof and use thereof in environmentally-friendly insulating varnish |
CN106279331A (zh) * | 2016-07-27 | 2017-01-04 | 宋火良 | 胆酸类肝病治疗药物 |
CN106279331B (zh) * | 2016-07-27 | 2019-06-14 | 宋火良 | 胆酸类肝病治疗药物 |
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