KR20140068988A - 상당한 내화성을 갖는 열가소성 폴리우레탄 - Google Patents
상당한 내화성을 갖는 열가소성 폴리우레탄 Download PDFInfo
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- KR20140068988A KR20140068988A KR1020147007206A KR20147007206A KR20140068988A KR 20140068988 A KR20140068988 A KR 20140068988A KR 1020147007206 A KR1020147007206 A KR 1020147007206A KR 20147007206 A KR20147007206 A KR 20147007206A KR 20140068988 A KR20140068988 A KR 20140068988A
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- Prior art keywords
- phosphonate
- polymer
- oligomer
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- Prior art date
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- 229920002803 thermoplastic polyurethane Polymers 0.000 title claims abstract description 116
- 239000004433 Thermoplastic polyurethane Substances 0.000 title claims abstract description 95
- UEZVMMHDMIWARA-UHFFFAOYSA-M phosphonate Chemical compound [O-]P(=O)=O UEZVMMHDMIWARA-UHFFFAOYSA-M 0.000 claims abstract description 203
- 229920000642 polymer Polymers 0.000 claims abstract description 145
- 239000000203 mixture Substances 0.000 claims abstract description 121
- 229920001577 copolymer Polymers 0.000 claims abstract description 62
- 238000002834 transmittance Methods 0.000 claims abstract description 16
- 230000003287 optical effect Effects 0.000 claims abstract description 11
- -1 aryl phosphonate Chemical compound 0.000 claims description 47
- 238000000034 method Methods 0.000 claims description 36
- 238000012360 testing method Methods 0.000 claims description 36
- 239000000463 material Substances 0.000 claims description 27
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- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 9
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- 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 8
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- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 7
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- XQUPVDVFXZDTLT-UHFFFAOYSA-N 1-[4-[[4-(2,5-dioxopyrrol-1-yl)phenyl]methyl]phenyl]pyrrole-2,5-dione Chemical compound O=C1C=CC(=O)N1C(C=C1)=CC=C1CC1=CC=C(N2C(C=CC2=O)=O)C=C1 XQUPVDVFXZDTLT-UHFFFAOYSA-N 0.000 claims description 6
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- XECAHXYUAAWDEL-UHFFFAOYSA-N acrylonitrile butadiene styrene Chemical compound C=CC=C.C=CC#N.C=CC1=CC=CC=C1 XECAHXYUAAWDEL-UHFFFAOYSA-N 0.000 claims description 6
- 239000004676 acrylonitrile butadiene styrene Substances 0.000 claims description 6
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- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 claims description 4
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 4
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- 229920003235 aromatic polyamide Polymers 0.000 claims description 4
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 4
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- 125000000524 functional group Chemical group 0.000 claims description 4
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- JRCBAJFWUZDKAP-UHFFFAOYSA-N OC(O)=O.OP(O)=O Chemical class OC(O)=O.OP(O)=O JRCBAJFWUZDKAP-UHFFFAOYSA-N 0.000 claims description 3
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- 150000000183 1,3-benzoxazoles Chemical class 0.000 claims description 2
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 claims description 2
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- 125000000555 isopropenyl group Chemical group [H]\C([H])=C(\*)C([H])([H])[H] 0.000 claims description 2
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- 101100323621 Drosophila melanogaster Drip gene Proteins 0.000 claims 1
- FPVBSWLPPTYVTL-UHFFFAOYSA-N NC(=O)OCC.[C] Chemical compound NC(=O)OCC.[C] FPVBSWLPPTYVTL-UHFFFAOYSA-N 0.000 claims 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims 1
- 239000004566 building material Substances 0.000 claims 1
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- 238000009472 formulation Methods 0.000 abstract description 29
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 14
- 125000003118 aryl group Chemical group 0.000 description 14
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 11
- 239000000178 monomer Substances 0.000 description 10
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 9
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical class OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 description 8
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- UPMLOUAZCHDJJD-UHFFFAOYSA-N 4,4'-Diphenylmethane Diisocyanate Chemical compound C1=CC(N=C=O)=CC=C1CC1=CC=C(N=C=O)C=C1 UPMLOUAZCHDJJD-UHFFFAOYSA-N 0.000 description 5
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- HTGQVPLFCQARQE-UHFFFAOYSA-N 2,3,4,5,6-pentachlorobenzenesulfonic acid Chemical compound OS(=O)(=O)C1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl HTGQVPLFCQARQE-UHFFFAOYSA-N 0.000 description 1
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- OUXGBSWADJDIMN-UHFFFAOYSA-N 2,3,4,5-tetrafluorobenzenesulfonic acid Chemical compound OS(=O)(=O)C1=CC(F)=C(F)C(F)=C1F OUXGBSWADJDIMN-UHFFFAOYSA-N 0.000 description 1
- LZRRHSPOUBLNBQ-UHFFFAOYSA-N 2,3,4,6-tetrachlorobenzenesulfonic acid Chemical compound OS(=O)(=O)C1=C(Cl)C=C(Cl)C(Cl)=C1Cl LZRRHSPOUBLNBQ-UHFFFAOYSA-N 0.000 description 1
- BWRJIDMRILXEDW-UHFFFAOYSA-N 2,3,4-trichlorobenzenesulfonic acid Chemical compound OS(=O)(=O)C1=CC=C(Cl)C(Cl)=C1Cl BWRJIDMRILXEDW-UHFFFAOYSA-N 0.000 description 1
- FWWLCAJMDFPHLI-UHFFFAOYSA-N 2,3,5,6-tetrachlorobenzenesulfonic acid Chemical compound OS(=O)(=O)C1=C(Cl)C(Cl)=CC(Cl)=C1Cl FWWLCAJMDFPHLI-UHFFFAOYSA-N 0.000 description 1
- UFNIBRDIUNVOMX-UHFFFAOYSA-N 2,4'-dichlorobiphenyl Chemical group C1=CC(Cl)=CC=C1C1=CC=CC=C1Cl UFNIBRDIUNVOMX-UHFFFAOYSA-N 0.000 description 1
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- XCLCLCNSGDHVFE-UHFFFAOYSA-N 2,4-dichlorobenzenesulfonic acid Chemical compound OS(=O)(=O)C1=CC=C(Cl)C=C1Cl XCLCLCNSGDHVFE-UHFFFAOYSA-N 0.000 description 1
- GUCJTGYQCHDCLD-UHFFFAOYSA-N 2,5-dibromobenzenesulfonic acid Chemical compound OS(=O)(=O)C1=CC(Br)=CC=C1Br GUCJTGYQCHDCLD-UHFFFAOYSA-N 0.000 description 1
- ZBAWSGLFJQGAJI-UHFFFAOYSA-N 2-bromo-4-chlorobenzenesulfonic acid Chemical compound OS(=O)(=O)C1=CC=C(Cl)C=C1Br ZBAWSGLFJQGAJI-UHFFFAOYSA-N 0.000 description 1
- SBYMUDUGTIKLCR-UHFFFAOYSA-N 2-chloroethenylbenzene Chemical compound ClC=CC1=CC=CC=C1 SBYMUDUGTIKLCR-UHFFFAOYSA-N 0.000 description 1
- UKHFMSRYRGAIEI-UHFFFAOYSA-N 4,5-dichlorobenzene-1,3-disulfonic acid Chemical compound OS(=O)(=O)C1=CC(Cl)=C(Cl)C(S(O)(=O)=O)=C1 UKHFMSRYRGAIEI-UHFFFAOYSA-N 0.000 description 1
- ZQYNTHZOEXICBG-UHFFFAOYSA-N 4-bromo-2-chlorobenzenesulfonic acid Chemical compound OS(=O)(=O)C1=CC=C(Br)C=C1Cl ZQYNTHZOEXICBG-UHFFFAOYSA-N 0.000 description 1
- PXACTUVBBMDKRW-UHFFFAOYSA-N 4-bromobenzenesulfonic acid Chemical compound OS(=O)(=O)C1=CC=C(Br)C=C1 PXACTUVBBMDKRW-UHFFFAOYSA-N 0.000 description 1
- RJWBTWIBUIGANW-UHFFFAOYSA-N 4-chlorobenzenesulfonic acid Chemical compound OS(=O)(=O)C1=CC=C(Cl)C=C1 RJWBTWIBUIGANW-UHFFFAOYSA-N 0.000 description 1
- WVSYONICNIDYBE-UHFFFAOYSA-N 4-fluorobenzenesulfonic acid Chemical compound OS(=O)(=O)C1=CC=C(F)C=C1 WVSYONICNIDYBE-UHFFFAOYSA-N 0.000 description 1
- 244000025254 Cannabis sativa Species 0.000 description 1
- 235000012766 Cannabis sativa ssp. sativa var. sativa Nutrition 0.000 description 1
- 235000012765 Cannabis sativa ssp. sativa var. spontanea Nutrition 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- LSDPWZHWYPCBBB-UHFFFAOYSA-N Methanethiol Chemical compound SC LSDPWZHWYPCBBB-UHFFFAOYSA-N 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 240000004885 Quercus rubra Species 0.000 description 1
- 235000009135 Quercus rubra Nutrition 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical class C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 238000005299 abrasion Methods 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 125000003342 alkenyl group Chemical group 0.000 description 1
- 125000003545 alkoxy group Chemical group 0.000 description 1
- 125000003282 alkyl amino group Chemical group 0.000 description 1
- 150000005215 alkyl ethers Chemical class 0.000 description 1
- 230000003373 anti-fouling effect Effects 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- PKJZRDCBPRGCCZ-UHFFFAOYSA-L barium(2+);2,4,5-trichlorobenzenesulfonate Chemical compound [Ba+2].[O-]S(=O)(=O)C1=CC(Cl)=C(Cl)C=C1Cl.[O-]S(=O)(=O)C1=CC(Cl)=C(Cl)C=C1Cl PKJZRDCBPRGCCZ-UHFFFAOYSA-L 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
- 239000004305 biphenyl Chemical group 0.000 description 1
- 235000010290 biphenyl Nutrition 0.000 description 1
- ZZUFUNZTPNRBID-UHFFFAOYSA-K bismuth;octanoate Chemical compound [Bi+3].CCCCCCCC([O-])=O.CCCCCCCC([O-])=O.CCCCCCCC([O-])=O ZZUFUNZTPNRBID-UHFFFAOYSA-K 0.000 description 1
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 1
- 229920001400 block copolymer Polymers 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- KOSKETBSVOTPHT-UHFFFAOYSA-L calcium;2,5-dichlorobenzenesulfonate Chemical compound [Ca+2].[O-]S(=O)(=O)C1=CC(Cl)=CC=C1Cl.[O-]S(=O)(=O)C1=CC(Cl)=CC=C1Cl KOSKETBSVOTPHT-UHFFFAOYSA-L 0.000 description 1
- 235000009120 camo Nutrition 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 235000005607 chanvre indien Nutrition 0.000 description 1
- 238000012512 characterization method Methods 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 125000004093 cyano group Chemical group *C#N 0.000 description 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
- 125000004663 dialkyl amino group Chemical group 0.000 description 1
- MHDVGSVTJDSBDK-UHFFFAOYSA-N dibenzyl ether Chemical compound C=1C=CC=CC=1COCC1=CC=CC=C1 MHDVGSVTJDSBDK-UHFFFAOYSA-N 0.000 description 1
- JGFBRKRYDCGYKD-UHFFFAOYSA-N dibutyl(oxo)tin Chemical compound CCCC[Sn](=O)CCCC JGFBRKRYDCGYKD-UHFFFAOYSA-N 0.000 description 1
- HGQSXVKHVMGQRG-UHFFFAOYSA-N dioctyltin Chemical compound CCCCCCCC[Sn]CCCCCCCC HGQSXVKHVMGQRG-UHFFFAOYSA-N 0.000 description 1
- USIUVYZYUHIAEV-UHFFFAOYSA-N diphenyl ether Chemical class C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 description 1
- DYDKYRXIBPVSKQ-UHFFFAOYSA-L disodium;2,5-dichlorobenzene-1,3-disulfonate Chemical compound [Na+].[Na+].[O-]S(=O)(=O)C1=CC(Cl)=CC(S([O-])(=O)=O)=C1Cl DYDKYRXIBPVSKQ-UHFFFAOYSA-L 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 239000000806 elastomer Substances 0.000 description 1
- 229920006351 engineering plastic Polymers 0.000 description 1
- 239000003623 enhancer Substances 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 239000010408 film Substances 0.000 description 1
- 230000009975 flexible effect Effects 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 238000011010 flushing procedure Methods 0.000 description 1
- 230000009477 glass transition Effects 0.000 description 1
- 239000004519 grease Substances 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- 239000011487 hemp Substances 0.000 description 1
- CKAPSXZOOQJIBF-UHFFFAOYSA-N hexachlorobenzene Chemical compound ClC1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl CKAPSXZOOQJIBF-UHFFFAOYSA-N 0.000 description 1
- 125000004836 hexamethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[*:1] 0.000 description 1
- 229920006158 high molecular weight polymer Polymers 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 150000002440 hydroxy compounds Chemical class 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 150000007529 inorganic bases Chemical class 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 238000009533 lab test Methods 0.000 description 1
- VDGYMDVRXAWGJD-UHFFFAOYSA-M lithium;2,4,5-trichlorobenzenesulfonate Chemical compound [Li+].[O-]S(=O)(=O)C1=CC(Cl)=C(Cl)C=C1Cl VDGYMDVRXAWGJD-UHFFFAOYSA-M 0.000 description 1
- MBVROLQFQZRITL-UHFFFAOYSA-M lithium;4-bromobenzenesulfonate Chemical compound [Li+].[O-]S(=O)(=O)C1=CC=C(Br)C=C1 MBVROLQFQZRITL-UHFFFAOYSA-M 0.000 description 1
- 238000011068 loading method Methods 0.000 description 1
- 239000010687 lubricating oil Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- ZQKXQUJXLSSJCH-UHFFFAOYSA-N melamine cyanurate Chemical compound NC1=NC(N)=NC(N)=N1.O=C1NC(=O)NC(=O)N1 ZQKXQUJXLSSJCH-UHFFFAOYSA-N 0.000 description 1
- 238000010128 melt processing Methods 0.000 description 1
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
- 229910000000 metal hydroxide Inorganic materials 0.000 description 1
- 150000004692 metal hydroxides Chemical class 0.000 description 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000001624 naphthyl group Chemical group 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 239000006259 organic additive Substances 0.000 description 1
- 150000002902 organometallic compounds Chemical class 0.000 description 1
- 125000002524 organometallic group Chemical group 0.000 description 1
- JOXIMZWYDAKGHI-UHFFFAOYSA-N p-toluenesulfonic acid Substances CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 1
- NFHFRUOZVGFOOS-UHFFFAOYSA-N palladium;triphenylphosphane Chemical compound [Pd].C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 NFHFRUOZVGFOOS-UHFFFAOYSA-N 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Chemical group C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 1
- 229940096825 phenylmercury Drugs 0.000 description 1
- DCNLOVYDMCVNRZ-UHFFFAOYSA-N phenylmercury(.) Chemical compound [Hg]C1=CC=CC=C1 DCNLOVYDMCVNRZ-UHFFFAOYSA-N 0.000 description 1
- 235000021317 phosphate Nutrition 0.000 description 1
- ACVYVLVWPXVTIT-UHFFFAOYSA-M phosphinate Chemical class [O-][PH2]=O ACVYVLVWPXVTIT-UHFFFAOYSA-M 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 229920003216 poly(methylphenylsiloxane) Polymers 0.000 description 1
- 229920000139 polyethylene terephthalate Polymers 0.000 description 1
- 239000005020 polyethylene terephthalate Substances 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 229920001843 polymethylhydrosiloxane Polymers 0.000 description 1
- 229920003225 polyurethane elastomer Polymers 0.000 description 1
- 230000008092 positive effect Effects 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 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
- QPTWOXZOCFKGHH-UHFFFAOYSA-N potassium;1,2,4-trichlorobenzene Chemical compound [K].ClC1=CC=C(Cl)C(Cl)=C1 QPTWOXZOCFKGHH-UHFFFAOYSA-N 0.000 description 1
- DRPLRPSXUUSFOB-UHFFFAOYSA-M potassium;2,4,5-trichlorobenzenesulfonate Chemical compound [K+].[O-]S(=O)(=O)C1=CC(Cl)=C(Cl)C=C1Cl DRPLRPSXUUSFOB-UHFFFAOYSA-M 0.000 description 1
- GGRIQDPLLHVRDU-UHFFFAOYSA-M potassium;2-(benzenesulfonyl)benzenesulfonate Chemical compound [K+].[O-]S(=O)(=O)C1=CC=CC=C1S(=O)(=O)C1=CC=CC=C1 GGRIQDPLLHVRDU-UHFFFAOYSA-M 0.000 description 1
- LOEIXPJQKVLCSA-UHFFFAOYSA-M potassium;4-chloro-3-nitrobenzenesulfonate Chemical compound [K+].[O-][N+](=O)C1=CC(S([O-])(=O)=O)=CC=C1Cl LOEIXPJQKVLCSA-UHFFFAOYSA-M 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 238000003672 processing method Methods 0.000 description 1
- 230000002285 radioactive effect Effects 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- 102220005284 rs33958088 Human genes 0.000 description 1
- UXQNSIKXUJGHOP-UHFFFAOYSA-M sodium;2,3,4,5,6-pentachlorobenzenesulfonate Chemical compound [Na+].[O-]S(=O)(=O)C1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl UXQNSIKXUJGHOP-UHFFFAOYSA-M 0.000 description 1
- GORSMCFYBKJFDT-UHFFFAOYSA-M sodium;2,3,4,5-tetrabromobenzenesulfonate Chemical compound [Na+].[O-]S(=O)(=O)C1=CC(Br)=C(Br)C(Br)=C1Br GORSMCFYBKJFDT-UHFFFAOYSA-M 0.000 description 1
- MGYQHXLLANOLKI-UHFFFAOYSA-M sodium;2,3,5,6-tetrachlorobenzenesulfonate Chemical compound [Na+].[O-]S(=O)(=O)C1=C(Cl)C(Cl)=CC(Cl)=C1Cl MGYQHXLLANOLKI-UHFFFAOYSA-M 0.000 description 1
- QXCFFLGAAJDPTG-UHFFFAOYSA-M sodium;2,3-dichlorobenzenesulfonate Chemical compound [Na+].[O-]S(=O)(=O)C1=CC=CC(Cl)=C1Cl QXCFFLGAAJDPTG-UHFFFAOYSA-M 0.000 description 1
- GYZZQOGWEGCIRR-UHFFFAOYSA-M sodium;2,4,5-tribromobenzenesulfonate Chemical compound [Na+].[O-]S(=O)(=O)C1=CC(Br)=C(Br)C=C1Br GYZZQOGWEGCIRR-UHFFFAOYSA-M 0.000 description 1
- OMVLAGBUFPUMGQ-UHFFFAOYSA-M sodium;2,4,5-trichlorobenzenesulfonate Chemical compound [Na+].[O-]S(=O)(=O)C1=CC(Cl)=C(Cl)C=C1Cl OMVLAGBUFPUMGQ-UHFFFAOYSA-M 0.000 description 1
- QGEMKZRYEIUDHH-UHFFFAOYSA-M sodium;2,4-dibromo-5-fluorobenzenesulfonate Chemical compound [Na+].[O-]S(=O)(=O)C1=CC(F)=C(Br)C=C1Br QGEMKZRYEIUDHH-UHFFFAOYSA-M 0.000 description 1
- UOJYMOBALINYGN-UHFFFAOYSA-M sodium;2,5-difluorobenzenesulfonate Chemical compound [Na+].[O-]S(=O)(=O)C1=CC(F)=CC=C1F UOJYMOBALINYGN-UHFFFAOYSA-M 0.000 description 1
- XMTCIMFZSPKHMH-UHFFFAOYSA-M sodium;2-bromo-5-(4-bromophenyl)benzenesulfonate Chemical compound [Na+].C1=C(Br)C(S(=O)(=O)[O-])=CC(C=2C=CC(Br)=CC=2)=C1 XMTCIMFZSPKHMH-UHFFFAOYSA-M 0.000 description 1
- VJJZODUTCHSDGG-UHFFFAOYSA-M sodium;2-chloro-4-cyanobenzenesulfonate Chemical compound [Na+].[O-]S(=O)(=O)C1=CC=C(C#N)C=C1Cl VJJZODUTCHSDGG-UHFFFAOYSA-M 0.000 description 1
- OUERFXCJVYJQJO-UHFFFAOYSA-M sodium;2-chloro-5-nitrobenzenesulfonate Chemical compound [Na+].[O-][N+](=O)C1=CC=C(Cl)C(S([O-])(=O)=O)=C1 OUERFXCJVYJQJO-UHFFFAOYSA-M 0.000 description 1
- MNCGMVDMOKPCSQ-UHFFFAOYSA-M sodium;2-phenylethenesulfonate Chemical compound [Na+].[O-]S(=O)(=O)C=CC1=CC=CC=C1 MNCGMVDMOKPCSQ-UHFFFAOYSA-M 0.000 description 1
- JPFBVTMFUQNZKT-UHFFFAOYSA-M sodium;4-chloro-3-methylbenzenesulfonate Chemical compound [Na+].CC1=CC(S([O-])(=O)=O)=CC=C1Cl JPFBVTMFUQNZKT-UHFFFAOYSA-M 0.000 description 1
- WKMRINMQMSLQBI-UHFFFAOYSA-M sodium;4-iodobenzenesulfonate Chemical compound [Na+].[O-]S(=O)(=O)C1=CC=C(I)C=C1 WKMRINMQMSLQBI-UHFFFAOYSA-M 0.000 description 1
- KVCGISUBCHHTDD-UHFFFAOYSA-M sodium;4-methylbenzenesulfonate Chemical compound [Na+].CC1=CC=C(S([O-])(=O)=O)C=C1 KVCGISUBCHHTDD-UHFFFAOYSA-M 0.000 description 1
- PMOVZAZKIRRMMO-UHFFFAOYSA-L strontium;2,4,5-trichlorobenzenesulfonate Chemical compound [Sr+2].[O-]S(=O)(=O)C1=CC(Cl)=C(Cl)C=C1Cl.[O-]S(=O)(=O)C1=CC(Cl)=C(Cl)C=C1Cl PMOVZAZKIRRMMO-UHFFFAOYSA-L 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- 125000001273 sulfonato group Chemical group [O-]S(*)(=O)=O 0.000 description 1
- 239000012970 tertiary amine catalyst Substances 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 229920002725 thermoplastic elastomer Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- XHAJNVLOLXIMHF-UHFFFAOYSA-K trisodium 2,4,6-trichlorobenzene-1,3,5-trisulfonate Chemical compound [Na+].[Na+].[Na+].[O-]S(=O)(=O)c1c(Cl)c(c(Cl)c(c1Cl)S([O-])(=O)=O)S([O-])(=O)=O XHAJNVLOLXIMHF-UHFFFAOYSA-K 0.000 description 1
- 150000003673 urethanes Chemical class 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
Classifications
-
- 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
- C08K5/00—Use of organic ingredients
- C08K5/49—Phosphorus-containing compounds
- C08K5/51—Phosphorus bound to oxygen
- C08K5/53—Phosphorus bound to oxygen bound to oxygen and to carbon only
- C08K5/5317—Phosphonic compounds, e.g. R—P(:O)(OR')2
-
- 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
- C08K7/00—Use of ingredients characterised by shape
- C08K7/02—Fibres or whiskers
-
- 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
- C08K7/00—Use of ingredients characterised by shape
- C08K7/02—Fibres or whiskers
- C08K7/04—Fibres or whiskers inorganic
- C08K7/06—Elements
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L75/00—Compositions of polyureas or polyurethanes; Compositions of derivatives of such polymers
- C08L75/04—Polyurethanes
- C08L75/06—Polyurethanes from polyesters
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L75/00—Compositions of polyureas or polyurethanes; Compositions of derivatives of such polymers
- C08L75/04—Polyurethanes
- C08L75/08—Polyurethanes from polyethers
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
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- Organic Chemistry (AREA)
- Compositions Of Macromolecular Compounds (AREA)
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| PCT/US2012/051587 WO2013028622A2 (en) | 2011-08-19 | 2012-08-20 | Thermoplastic polyurethanes with exceptional fire resistance |
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| TW (1) | TWI638005B (cg-RX-API-DMAC10.html) |
| WO (1) | WO2013028622A2 (cg-RX-API-DMAC10.html) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2019132586A1 (ko) * | 2017-12-29 | 2019-07-04 | 롯데첨단소재(주) | 열가소성 수지 조성물 및 이로부터 형성된 성형품 |
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| WO2015057717A1 (en) * | 2013-10-14 | 2015-04-23 | Frx Polymers, Inc. | Flame retardant thermoplastic elastomers for extrusion or injection molding |
| JP6355123B2 (ja) * | 2014-03-31 | 2018-07-11 | ジャパンコーティングレジン株式会社 | ウレタン樹脂及びそのエマルジョン |
| CN105802128B (zh) * | 2014-12-29 | 2018-05-04 | 广东生益科技股份有限公司 | 一种无卤热固性树脂组合物及使用它的预浸料和印制电路用层压板 |
| KR20180008602A (ko) * | 2015-05-18 | 2018-01-24 | 미츠비시 가스 가가쿠 가부시키가이샤 | 폴리카보네이트 수지 조성물, 및 폴리카보네이트 수지제 프리프레그 |
| WO2017055356A1 (en) * | 2015-10-01 | 2017-04-06 | Dsm Ip Assets B.V. | Halogen free flame retardant waterborne coating composition for textile |
| CN105566890A (zh) * | 2016-02-24 | 2016-05-11 | 江苏道勤新材料科技有限公司 | 一种高强度雾面塑料材料 |
| CN105566889A (zh) * | 2016-02-24 | 2016-05-11 | 江苏道勤新材料科技有限公司 | 一种雾面塑料材料 |
| CN105754323B (zh) * | 2016-03-08 | 2019-01-29 | 深圳市沃尔核材股份有限公司 | 一种高强度阻燃耐磨耐水解标识卡及其生产方法 |
| CN106009587A (zh) * | 2016-06-14 | 2016-10-12 | 江苏金发科技新材料有限公司 | 高cti值高耐热性聚碳酸酯组合物及其制备方法 |
| CN106381074A (zh) * | 2016-08-30 | 2017-02-08 | 无锡万能胶粘剂有限公司 | 一种阻燃的万能胶 |
| EP3385295A1 (de) | 2017-04-05 | 2018-10-10 | Covestro Deutschland AG | Flammgeschützte phosphorfunktionelle polyethercarbonatpolyole und verfahren zu deren herstellung |
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| CN109705562A (zh) * | 2017-10-26 | 2019-05-03 | 江苏瑞凌新能源科技有限公司 | 一种阻燃汽车配件塑料配方 |
| EP3498788B1 (en) * | 2017-12-18 | 2023-05-03 | Agfa-Gevaert Nv | Solder mask inkjet inks for manufacturing printed circuit boards |
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| CN108059821B (zh) * | 2017-12-29 | 2021-02-12 | 东莞市雄林新材料科技股份有限公司 | 一种在磁场作用下硬度增强的tpu材料及其制备方法 |
| EP3774657A4 (en) * | 2018-03-30 | 2021-12-22 | Sergei Nazarenko | FLAME RETARDANT AGENTS CONTAINING SOLUBLE FLAME RETARDANT METAL COMPOUNDS |
| WO2019204625A1 (en) * | 2018-04-18 | 2019-10-24 | Frx Polymers, Inc. | Halogen-free flame-retardant compositions for flexible polyurethane foams |
| CN109054358A (zh) * | 2018-07-11 | 2018-12-21 | 望江县天长光学仪器有限公司 | 一种增强型光学透镜材料 |
| EP3604320A1 (de) | 2018-08-01 | 2020-02-05 | Covestro Deutschland AG | Phosphorfunktionelle polyoxyalkylenpolyole und verfahren zu deren herstellung |
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| CN111363453A (zh) * | 2020-04-01 | 2020-07-03 | 中国石油天然气股份有限公司长庆石化分公司 | 一种可紫外光固化的高温容器内衬材料及其制备方法 |
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| JP2024530693A (ja) * | 2021-08-13 | 2024-08-23 | ヒューズ、ロバート、ケー、ジュニア | 繊維強化エポキシ供給システム |
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| CN103619959A (zh) * | 2011-04-14 | 2014-03-05 | Frx聚合物股份有限公司 | 聚膦酸酯和共聚膦酸酯添加剂混合物 |
| JP6600440B2 (ja) * | 2012-06-29 | 2019-10-30 | エフアールエックス ポリマーズ、インク． | ポリエステルコ−ホスホネート |
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- 2012-08-20 KR KR1020147007206A patent/KR20140068988A/ko not_active Ceased
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- 2012-08-20 CN CN201280039890.6A patent/CN103732686A/zh active Pending
- 2012-08-20 JP JP2014526272A patent/JP6151696B2/ja not_active Expired - Fee Related
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2019132586A1 (ko) * | 2017-12-29 | 2019-07-04 | 롯데첨단소재(주) | 열가소성 수지 조성물 및 이로부터 형성된 성형품 |
Also Published As
| Publication number | Publication date |
|---|---|
| TW201319163A (zh) | 2013-05-16 |
| TWI638005B (zh) | 2018-10-11 |
| EP2744862A4 (en) | 2015-01-21 |
| JP6151696B2 (ja) | 2017-06-21 |
| WO2013028622A3 (en) | 2013-05-30 |
| CN103732686A (zh) | 2014-04-16 |
| EP2744862A2 (en) | 2014-06-25 |
| US9267017B2 (en) | 2016-02-23 |
| WO2013028622A2 (en) | 2013-02-28 |
| US20130046036A1 (en) | 2013-02-21 |
| JP2014521827A (ja) | 2014-08-28 |
| WO2013028622A9 (en) | 2013-04-11 |
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