CN104231313A - 三嗪三苯基次膦酸丙酯阻燃剂组合物及其应用方法 - Google Patents
三嗪三苯基次膦酸丙酯阻燃剂组合物及其应用方法 Download PDFInfo
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- CN104231313A CN104231313A CN201410507955.6A CN201410507955A CN104231313A CN 104231313 A CN104231313 A CN 104231313A CN 201410507955 A CN201410507955 A CN 201410507955A CN 104231313 A CN104231313 A CN 104231313A
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- 239000003063 flame retardant Substances 0.000 title claims abstract description 55
- 239000000203 mixture Substances 0.000 title claims abstract description 32
- 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 title claims abstract description 31
- QOSMNYMQXIVWKY-UHFFFAOYSA-N Propyl levulinate Chemical compound CCCOC(=O)CCC(C)=O QOSMNYMQXIVWKY-UHFFFAOYSA-N 0.000 title claims abstract description 14
- 238000000034 method Methods 0.000 title claims abstract description 10
- 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 abstract 3
- 229920000728 polyester Polymers 0.000 claims abstract description 27
- -1 polypropylene Polymers 0.000 claims abstract description 16
- ZQKXQUJXLSSJCH-UHFFFAOYSA-N melamine cyanurate Chemical compound NC1=NC(N)=NC(N)=N1.O=C1NC(=O)NC(=O)N1 ZQKXQUJXLSSJCH-UHFFFAOYSA-N 0.000 claims abstract description 4
- 238000002156 mixing Methods 0.000 claims abstract description 3
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 claims abstract description 3
- LFQCEHFDDXELDD-UHFFFAOYSA-N tetramethyl orthosilicate Chemical compound CO[Si](OC)(OC)OC LFQCEHFDDXELDD-UHFFFAOYSA-N 0.000 claims abstract description 3
- 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 description 29
- 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 description 29
- 238000002229 photoelectron microspectroscopy Methods 0.000 claims description 29
- 239000002131 composite material Substances 0.000 claims description 17
- 239000002253 acid Substances 0.000 claims description 11
- 150000001875 compounds Chemical class 0.000 claims description 4
- 229920000877 Melamine resin Polymers 0.000 claims description 2
- 229920000388 Polyphosphate Polymers 0.000 claims description 2
- 125000005842 heteroatom Chemical group 0.000 claims description 2
- 238000001746 injection moulding Methods 0.000 claims description 2
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 claims description 2
- 239000001205 polyphosphate Substances 0.000 claims description 2
- 235000011176 polyphosphates Nutrition 0.000 claims description 2
- 239000000463 material Substances 0.000 abstract description 13
- 230000002195 synergetic effect Effects 0.000 abstract description 5
- 239000004743 Polypropylene Substances 0.000 abstract description 4
- 239000003822 epoxy resin Substances 0.000 abstract description 4
- 229910052736 halogen Inorganic materials 0.000 abstract description 4
- 150000002367 halogens Chemical class 0.000 abstract description 4
- 229920000647 polyepoxide Polymers 0.000 abstract description 4
- 229920001155 polypropylene Polymers 0.000 abstract description 4
- 230000007613 environmental effect Effects 0.000 abstract description 3
- XZTOTRSSGPPNTB-UHFFFAOYSA-N phosphono dihydrogen phosphate;1,3,5-triazine-2,4,6-triamine Chemical compound NC1=NC(N)=NC(N)=N1.OP(O)(=O)OP(O)(O)=O XZTOTRSSGPPNTB-UHFFFAOYSA-N 0.000 abstract 2
- BSYJHYLAMMJNRC-UHFFFAOYSA-N 2,4,4-trimethylpentan-2-ol Chemical compound CC(C)(C)CC(C)(C)O BSYJHYLAMMJNRC-UHFFFAOYSA-N 0.000 abstract 1
- 239000007977 PBT buffer Substances 0.000 abstract 1
- 238000013329 compounding Methods 0.000 abstract 1
- 229920001707 polybutylene terephthalate Polymers 0.000 abstract 1
- 229920002635 polyurethane Polymers 0.000 abstract 1
- 239000004814 polyurethane Substances 0.000 abstract 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 28
- 229910052760 oxygen Inorganic materials 0.000 description 28
- 239000001301 oxygen Substances 0.000 description 28
- 238000003756 stirring Methods 0.000 description 14
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 6
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 3
- XYFCBTPGUUZFHI-UHFFFAOYSA-N Phosphine Natural products P XYFCBTPGUUZFHI-UHFFFAOYSA-N 0.000 description 3
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 3
- 238000011161 development Methods 0.000 description 3
- 229910052757 nitrogen Inorganic materials 0.000 description 3
- 229910052698 phosphorus Inorganic materials 0.000 description 3
- 239000011574 phosphorus Substances 0.000 description 3
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 229910000073 phosphorus hydride Inorganic materials 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
- JYEUMXHLPRZUAT-UHFFFAOYSA-N 1,2,3-triazine Chemical group C1=CN=NN=C1 JYEUMXHLPRZUAT-UHFFFAOYSA-N 0.000 description 1
- 0 CC(*)P([N+](c1nc(N)nc(N)n1)[O-])(OC)=O Chemical compound CC(*)P([N+](c1nc(N)nc(N)n1)[O-])(OC)=O 0.000 description 1
- KUXDQQMEFBFTGX-UHFFFAOYSA-N [N].P Chemical group [N].P KUXDQQMEFBFTGX-UHFFFAOYSA-N 0.000 description 1
- YUWBVKYVJWNVLE-UHFFFAOYSA-N [N].[P] Chemical compound [N].[P] YUWBVKYVJWNVLE-UHFFFAOYSA-N 0.000 description 1
- 238000004458 analytical method Methods 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
- 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
- 239000006185 dispersion Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 238000009413 insulation Methods 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- 231100000053 low toxicity Toxicity 0.000 description 1
- 238000003754 machining Methods 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 229920000137 polyphosphoric acid Polymers 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 239000011241 protective layer Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
Abstract
Description
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Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
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CN201410507955.6A CN104231313B (zh) | 2014-09-26 | 2014-09-26 | 三嗪三苯基次膦酸丙酯阻燃剂组合物及其应用方法 |
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CN201410507955.6A CN104231313B (zh) | 2014-09-26 | 2014-09-26 | 三嗪三苯基次膦酸丙酯阻燃剂组合物及其应用方法 |
Publications (2)
Publication Number | Publication Date |
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CN104231313A true CN104231313A (zh) | 2014-12-24 |
CN104231313B CN104231313B (zh) | 2017-04-05 |
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CN201410507955.6A Active CN104231313B (zh) | 2014-09-26 | 2014-09-26 | 三嗪三苯基次膦酸丙酯阻燃剂组合物及其应用方法 |
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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 |
CN103265574A (zh) * | 2013-06-05 | 2013-08-28 | 苏州科技学院 | 三嗪三苯基次膦酸丙酯化合物及其制备方法 |
-
2014
- 2014-09-26 CN CN201410507955.6A patent/CN104231313B/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 |
CN103265574A (zh) * | 2013-06-05 | 2013-08-28 | 苏州科技学院 | 三嗪三苯基次膦酸丙酯化合物及其制备方法 |
Non-Patent Citations (2)
Title |
---|
W. HEWERTSON ET AL.: "1,3,5-Triazines. III. Arbuzov reactions of chlorotriazines", 《JOURNAL OF THE CHEMICAL SOCIETY》 * |
王彦林,等: "2,4,6-三(O,O-二甲基磷酰基)-1,3,5-三嗪的合成及表征", 《兰州理工大学学报》 * |
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CN104231313B (zh) | 2017-04-05 |
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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. |