CN104231311B - 三嗪三苯基次膦酸甲酯阻燃剂组合物及其应用方法 - Google Patents
三嗪三苯基次膦酸甲酯阻燃剂组合物及其应用方法 Download PDFInfo
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- CN104231311B CN104231311B CN201410507952.2A CN201410507952A CN104231311B CN 104231311 B CN104231311 B CN 104231311B CN 201410507952 A CN201410507952 A CN 201410507952A CN 104231311 B CN104231311 B CN 104231311B
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- 239000003063 flame retardant Substances 0.000 title claims abstract description 51
- SLTXIOBRDOEBQM-UHFFFAOYSA-N C1(=CC=CC=C1)OP(=O)(C1=CC=CC=C1)C1=CC=CC=C1.N1=NN=CC=C1 Chemical compound C1(=CC=CC=C1)OP(=O)(C1=CC=CC=C1)C1=CC=CC=C1.N1=NN=CC=C1 SLTXIOBRDOEBQM-UHFFFAOYSA-N 0.000 title claims abstract description 14
- 238000000034 method Methods 0.000 title claims abstract description 10
- BUCXEFZXWKUCCY-UHFFFAOYSA-N 4-methyl-3-(2-phenylethyl)-1,2,4-oxadiazol-5-one Chemical compound O1C(=O)N(C)C(CCC=2C=CC=CC=2)=N1 BUCXEFZXWKUCCY-UHFFFAOYSA-N 0.000 claims abstract description 28
- DWSWCPPGLRSPIT-UHFFFAOYSA-N benzo[c][2,1]benzoxaphosphinin-6-ium 6-oxide Chemical compound C1=CC=C2[P+](=O)OC3=CC=CC=C3C2=C1 DWSWCPPGLRSPIT-UHFFFAOYSA-N 0.000 claims abstract description 28
- 238000002229 photoelectron microspectroscopy Methods 0.000 claims abstract description 28
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- -1 phospho Chemical class 0.000 claims abstract description 8
- 229920000877 Melamine resin Polymers 0.000 claims abstract description 3
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- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 claims abstract description 3
- 239000001205 polyphosphate Substances 0.000 claims abstract description 3
- 235000011176 polyphosphates Nutrition 0.000 claims abstract description 3
- XZMCDFZZKTWFGF-UHFFFAOYSA-N Cyanamide Chemical compound NC#N XZMCDFZZKTWFGF-UHFFFAOYSA-N 0.000 claims 1
- 238000001125 extrusion Methods 0.000 claims 1
- ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Chemical compound OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 claims 1
- NCWQJOGVLLNWEO-UHFFFAOYSA-N methylsilicon Chemical compound [Si]C NCWQJOGVLLNWEO-UHFFFAOYSA-N 0.000 claims 1
- 238000005829 trimerization reaction Methods 0.000 claims 1
- 239000000463 material Substances 0.000 abstract description 13
- 239000004743 Polypropylene Substances 0.000 abstract description 4
- 230000007613 environmental effect Effects 0.000 abstract description 4
- 239000003822 epoxy resin Substances 0.000 abstract description 4
- 229920000647 polyepoxide Polymers 0.000 abstract description 4
- 229920001155 polypropylene Polymers 0.000 abstract description 4
- 230000002195 synergetic effect Effects 0.000 abstract description 4
- 239000007977 PBT buffer Substances 0.000 abstract description 3
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- 229920002635 polyurethane Polymers 0.000 abstract description 3
- 239000004814 polyurethane Substances 0.000 abstract description 3
- ZQKXQUJXLSSJCH-UHFFFAOYSA-N melamine cyanurate Chemical compound NC1=NC(N)=NC(N)=N1.O=C1NC(=O)NC(=O)N1 ZQKXQUJXLSSJCH-UHFFFAOYSA-N 0.000 abstract description 2
- YNPNZTXNASCQKK-UHFFFAOYSA-N phenanthrene Chemical compound C1=CC=C2C3=CC=CC=C3C=CC2=C1 YNPNZTXNASCQKK-UHFFFAOYSA-N 0.000 abstract 2
- 125000005842 heteroatom Chemical group 0.000 abstract 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 abstract 1
- LFQCEHFDDXELDD-UHFFFAOYSA-N tetramethyl orthosilicate Chemical compound CO[Si](OC)(OC)OC LFQCEHFDDXELDD-UHFFFAOYSA-N 0.000 abstract 1
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- 238000003756 stirring Methods 0.000 description 14
- XYFCBTPGUUZFHI-UHFFFAOYSA-N Phosphine Chemical compound P XYFCBTPGUUZFHI-UHFFFAOYSA-N 0.000 description 10
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 6
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- 229910000073 phosphorus hydride Inorganic materials 0.000 description 5
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 4
- 229910052698 phosphorus Inorganic materials 0.000 description 4
- 239000011574 phosphorus Substances 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 3
- 229910052757 nitrogen Inorganic materials 0.000 description 3
- 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 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 2
- 238000004458 analytical method Methods 0.000 description 2
- 238000000280 densification Methods 0.000 description 2
- 238000011161 development Methods 0.000 description 2
- 235000013399 edible fruits Nutrition 0.000 description 2
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- 150000002148 esters Chemical class 0.000 description 2
- 229910052736 halogen Inorganic materials 0.000 description 2
- 150000002367 halogens Chemical class 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 238000011160 research Methods 0.000 description 2
- 229910052710 silicon Inorganic materials 0.000 description 2
- 239000010703 silicon Substances 0.000 description 2
- BSYJHYLAMMJNRC-UHFFFAOYSA-N 2,4,4-trimethylpentan-2-ol Chemical compound CC(C)(C)CC(C)(C)O BSYJHYLAMMJNRC-UHFFFAOYSA-N 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- KUXDQQMEFBFTGX-UHFFFAOYSA-N [N].P Chemical compound [N].P KUXDQQMEFBFTGX-UHFFFAOYSA-N 0.000 description 1
- 230000006978 adaptation Effects 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 239000003610 charcoal Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000007812 deficiency Effects 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000003754 machining Methods 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 238000013508 migration Methods 0.000 description 1
- 230000005012 migration Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
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- 229920000137 polyphosphoric acid Polymers 0.000 description 1
- 239000011241 protective layer Substances 0.000 description 1
- 239000000779 smoke Substances 0.000 description 1
Abstract
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CN201410507952.2A CN104231311B (zh) | 2014-09-26 | 2014-09-26 | 三嗪三苯基次膦酸甲酯阻燃剂组合物及其应用方法 |
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CN201410507952.2A CN104231311B (zh) | 2014-09-26 | 2014-09-26 | 三嗪三苯基次膦酸甲酯阻燃剂组合物及其应用方法 |
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CN104231311A CN104231311A (zh) | 2014-12-24 |
CN104231311B true CN104231311B (zh) | 2017-04-05 |
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Families Citing this family (4)
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CN109517009A (zh) * | 2018-10-23 | 2019-03-26 | 苏州科技大学 | 阻燃剂亚磷酸三硅笼醇酯化合物及其制备方法 |
CN112280356B (zh) * | 2020-09-30 | 2021-09-14 | 先登高科电气有限公司 | 一种阻燃漆包面涂层用复合阻燃剂及其制备方法和应用 |
CN114213710B (zh) * | 2021-12-16 | 2023-06-16 | 锦西化工研究院有限公司 | 一种阻燃剂及耐高温阻燃透明聚碳酸酯树脂 |
CN114478061B (zh) * | 2022-04-01 | 2022-12-13 | 舒城诚鑫建材有限公司 | 改性防火匀质板及其生产工艺 |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3410809A (en) * | 1965-05-28 | 1968-11-12 | Monsanto Res Corp | Cn compounds |
WO2006130353A2 (en) * | 2005-05-31 | 2006-12-07 | Eastman Kodak Company | Light-emitting device containing bis-phosphineoxide compound |
CN103254234A (zh) * | 2013-06-05 | 2013-08-21 | 苏州科技学院 | 三嗪三苯基次膦酸甲酯化合物及其制备方法 |
-
2014
- 2014-09-26 CN CN201410507952.2A patent/CN104231311B/zh active Active
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3410809A (en) * | 1965-05-28 | 1968-11-12 | Monsanto Res Corp | Cn compounds |
WO2006130353A2 (en) * | 2005-05-31 | 2006-12-07 | Eastman Kodak Company | Light-emitting device containing bis-phosphineoxide compound |
CN103254234A (zh) * | 2013-06-05 | 2013-08-21 | 苏州科技学院 | 三嗪三苯基次膦酸甲酯化合物及其制备方法 |
Non-Patent Citations (2)
Title |
---|
1,3,5-Triazines. III. Arbuzov reactions of chlorotriazines;W. Hewertson et al.;《Journal of the Chemical Society》;19631231;1670-1675 * |
2,4,6-三(O,O-二甲基磷酰基)-1,3,5-三嗪的合成及表征;王彦林等;《兰州理工大学学报》;20100630;第36卷(第3期);78-80 * |
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Effective date of registration: 20210105 Address after: 257000 Wanda harbor city, No. 25-1, Gangcheng Road, Dongying Port Economic Development Zone, Dongying City, Shandong Province Patentee after: Shandong Xingqiang Chemical Industry Technology Research Institute Co.,Ltd. Address before: 215131 Room 610, Yuanhe Building, 959 Jiayuan Road, Xiangcheng District, Suzhou City, Jiangsu Province Patentee before: XIANGCHENG RESEARCH INSTITUTE SUZHOU University OF SCIENCE AND TECHNOLOGY |
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Effective date of registration: 20231101 Address after: Room 707, No. 15 Gangcheng Road, Dongying Port Economic Development Zone, Dongying City, Shandong Province, 257237 Patentee after: Shandong Industry Research Institute Zhongke High-end Chemical Industry Technology Research Institute Co.,Ltd. Address before: 257000 Wanda harbor city, No. 25-1, Gangcheng Road, Dongying Port Economic Development Zone, Dongying City, Shandong Province Patentee before: Shandong Xingqiang Chemical Industry Technology Research Institute Co.,Ltd. |