KR100540156B1 - 방염제 조성물 - Google Patents
방염제 조성물 Download PDFInfo
- Publication number
- KR100540156B1 KR100540156B1 KR10-1999-7012483A KR19997012483A KR100540156B1 KR 100540156 B1 KR100540156 B1 KR 100540156B1 KR 19997012483 A KR19997012483 A KR 19997012483A KR 100540156 B1 KR100540156 B1 KR 100540156B1
- Authority
- KR
- South Korea
- Prior art keywords
- flame retardant
- flame
- hindered amine
- bis
- carbon atoms
- 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 - Lifetime
Links
- 239000003063 flame retardant Substances 0.000 title claims abstract description 136
- 239000000203 mixture Substances 0.000 title claims abstract description 91
- 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 89
- -1 amine compounds Chemical class 0.000 claims abstract description 158
- 150000001412 amines Chemical class 0.000 claims abstract description 68
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 41
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 40
- 229920000642 polymer Polymers 0.000 claims abstract description 27
- 229910052698 phosphorus Inorganic materials 0.000 claims abstract description 18
- 239000011574 phosphorus Substances 0.000 claims abstract description 18
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims abstract description 17
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims abstract description 13
- 230000002195 synergetic effect Effects 0.000 claims abstract description 9
- 125000003545 alkoxy group Chemical group 0.000 claims abstract description 7
- RGSFGYAAUTVSQA-UHFFFAOYSA-N pentamethylene Natural products C1CCCC1 RGSFGYAAUTVSQA-UHFFFAOYSA-N 0.000 claims abstract description 7
- 125000000000 cycloalkoxy group Chemical group 0.000 claims abstract description 6
- 150000002148 esters Chemical group 0.000 claims abstract description 6
- 125000004817 pentamethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[*:1] 0.000 claims abstract description 6
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 claims abstract description 3
- 150000001408 amides Chemical group 0.000 claims abstract description 3
- 229940058905 antimony compound for treatment of leishmaniasis and trypanosomiasis Drugs 0.000 claims abstract description 3
- 150000001463 antimony compounds Chemical class 0.000 claims abstract description 3
- 125000004104 aryloxy group Chemical group 0.000 claims abstract description 3
- 229910052796 boron Inorganic materials 0.000 claims abstract description 3
- JOYRKODLDBILNP-UHFFFAOYSA-N urethane group Chemical group NC(=O)OCC JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 claims abstract description 3
- 238000000034 method Methods 0.000 claims description 17
- 229910052751 metal Inorganic materials 0.000 claims description 14
- 239000002184 metal Substances 0.000 claims description 14
- 125000002102 aryl alkyloxo group Chemical group 0.000 claims description 5
- 230000000979 retarding effect Effects 0.000 claims description 5
- 229920000307 polymer substrate Polymers 0.000 claims description 4
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims description 3
- 150000004677 hydrates Chemical class 0.000 claims description 3
- 229910044991 metal oxide Inorganic materials 0.000 claims description 3
- 150000004706 metal oxides Chemical class 0.000 claims description 3
- 229910052710 silicon Inorganic materials 0.000 claims description 3
- 239000010703 silicon Substances 0.000 claims description 3
- 229910000000 metal hydroxide Inorganic materials 0.000 claims description 2
- 150000004692 metal hydroxides Chemical class 0.000 claims description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 abstract description 52
- 239000000758 substrate Substances 0.000 abstract description 20
- 125000003710 aryl alkyl group Chemical group 0.000 abstract description 9
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical group CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 abstract description 8
- 229920000098 polyolefin Polymers 0.000 abstract description 7
- 229920001296 polysiloxane Polymers 0.000 abstract 1
- 238000009472 formulation Methods 0.000 description 50
- 150000001875 compounds Chemical class 0.000 description 43
- 239000000835 fiber Substances 0.000 description 32
- 229920001577 copolymer Polymers 0.000 description 31
- 239000004743 Polypropylene Substances 0.000 description 28
- 239000000654 additive Substances 0.000 description 28
- 238000002485 combustion reaction Methods 0.000 description 26
- 229920001155 polypropylene Polymers 0.000 description 26
- 229910052739 hydrogen Inorganic materials 0.000 description 25
- 239000001257 hydrogen Substances 0.000 description 25
- 238000012360 testing method Methods 0.000 description 22
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 21
- 239000005977 Ethylene Substances 0.000 description 21
- 239000004698 Polyethylene Substances 0.000 description 20
- 125000003118 aryl group Chemical group 0.000 description 20
- 238000002474 experimental method Methods 0.000 description 20
- 229920000573 polyethylene Polymers 0.000 description 20
- 150000002431 hydrogen Chemical class 0.000 description 19
- 239000000126 substance Substances 0.000 description 19
- 238000010998 test method Methods 0.000 description 16
- DYIZJUDNMOIZQO-UHFFFAOYSA-N 4,5,6,7-tetrabromo-2-[2-(4,5,6,7-tetrabromo-1,3-dioxoisoindol-2-yl)ethyl]isoindole-1,3-dione Chemical compound O=C1C(C(=C(Br)C(Br)=C2Br)Br)=C2C(=O)N1CCN1C(=O)C2=C(Br)C(Br)=C(Br)C(Br)=C2C1=O DYIZJUDNMOIZQO-UHFFFAOYSA-N 0.000 description 15
- 229920002397 thermoplastic olefin Polymers 0.000 description 15
- 239000004604 Blowing Agent Substances 0.000 description 14
- 125000002947 alkylene group Chemical group 0.000 description 14
- WHHGLZMJPXIBIX-UHFFFAOYSA-N decabromodiphenyl ether Chemical compound BrC1=C(Br)C(Br)=C(Br)C(Br)=C1OC1=C(Br)C(Br)=C(Br)C(Br)=C1Br WHHGLZMJPXIBIX-UHFFFAOYSA-N 0.000 description 14
- 229920001684 low density polyethylene Polymers 0.000 description 13
- 239000004702 low-density polyethylene Substances 0.000 description 13
- 229920005989 resin Polymers 0.000 description 13
- 239000011347 resin Substances 0.000 description 13
- ADCOVFLJGNWWNZ-UHFFFAOYSA-N antimony trioxide Chemical compound O=[Sb]O[Sb]=O ADCOVFLJGNWWNZ-UHFFFAOYSA-N 0.000 description 12
- 239000000047 product Substances 0.000 description 12
- YUAPUIKGYCAHGM-UHFFFAOYSA-N 1,2-dibromo-3-(2,3-dibromopropoxy)propane Chemical compound BrCC(Br)COCC(Br)CBr YUAPUIKGYCAHGM-UHFFFAOYSA-N 0.000 description 10
- 125000001931 aliphatic group Chemical group 0.000 description 10
- 230000000694 effects Effects 0.000 description 10
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 10
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 9
- 239000004114 Ammonium polyphosphate Substances 0.000 description 9
- 229910019142 PO4 Inorganic materials 0.000 description 9
- 235000019826 ammonium polyphosphate Nutrition 0.000 description 9
- 229920001276 ammonium polyphosphate Polymers 0.000 description 9
- 239000008188 pellet Substances 0.000 description 9
- 235000021317 phosphate Nutrition 0.000 description 9
- 101100162200 Aspergillus parasiticus (strain ATCC 56775 / NRRL 5862 / SRRC 143 / SU-1) aflD gene Proteins 0.000 description 8
- 239000005062 Polybutadiene Substances 0.000 description 8
- 239000004793 Polystyrene Substances 0.000 description 8
- 238000007906 compression Methods 0.000 description 8
- 230000006835 compression Effects 0.000 description 8
- 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 8
- 239000000463 material Substances 0.000 description 8
- 229910052757 nitrogen Inorganic materials 0.000 description 8
- 239000004745 nonwoven fabric Substances 0.000 description 8
- 239000010452 phosphate Substances 0.000 description 8
- 229920002857 polybutadiene Polymers 0.000 description 8
- 229920002223 polystyrene Polymers 0.000 description 8
- HCUOEKSZWPGJIM-IYNMRSRQSA-N (e,2z)-2-hydroxyimino-6-methoxy-4-methyl-5-nitrohex-3-enamide Chemical compound COCC([N+]([O-])=O)\C(C)=C\C(=N\O)\C(N)=O HCUOEKSZWPGJIM-IYNMRSRQSA-N 0.000 description 7
- 239000006096 absorbing agent Substances 0.000 description 7
- 125000000753 cycloalkyl group Chemical group 0.000 description 7
- VEORPZCZECFIRK-UHFFFAOYSA-N 3,3',5,5'-tetrabromobisphenol A Chemical compound C=1C(Br)=C(O)C(Br)=CC=1C(C)(C)C1=CC(Br)=C(O)C(Br)=C1 VEORPZCZECFIRK-UHFFFAOYSA-N 0.000 description 6
- KSSJBGNOJJETTC-UHFFFAOYSA-N COC1=C(C=CC=C1)N(C1=CC=2C3(C4=CC(=CC=C4C=2C=C1)N(C1=CC=C(C=C1)OC)C1=C(C=CC=C1)OC)C1=CC(=CC=C1C=1C=CC(=CC=13)N(C1=CC=C(C=C1)OC)C1=C(C=CC=C1)OC)N(C1=CC=C(C=C1)OC)C1=C(C=CC=C1)OC)C1=CC=C(C=C1)OC Chemical compound COC1=C(C=CC=C1)N(C1=CC=2C3(C4=CC(=CC=C4C=2C=C1)N(C1=CC=C(C=C1)OC)C1=C(C=CC=C1)OC)C1=CC(=CC=C1C=1C=CC(=CC=13)N(C1=CC=C(C=C1)OC)C1=C(C=CC=C1)OC)N(C1=CC=C(C=C1)OC)C1=C(C=CC=C1)OC)C1=CC=C(C=C1)OC KSSJBGNOJJETTC-UHFFFAOYSA-N 0.000 description 6
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 6
- 239000007983 Tris buffer Substances 0.000 description 6
- 239000002253 acid Substances 0.000 description 6
- 230000000996 additive effect Effects 0.000 description 6
- OSIVCXJNIBEGCL-UHFFFAOYSA-N bis(2,2,6,6-tetramethyl-1-octoxypiperidin-4-yl) decanedioate Chemical compound C1C(C)(C)N(OCCCCCCCC)C(C)(C)CC1OC(=O)CCCCCCCCC(=O)OC1CC(C)(C)N(OCCCCCCCC)C(C)(C)C1 OSIVCXJNIBEGCL-UHFFFAOYSA-N 0.000 description 6
- 125000006309 butyl amino group Chemical group 0.000 description 6
- 150000001993 dienes Chemical class 0.000 description 6
- 239000004744 fabric Substances 0.000 description 6
- 239000007789 gas Substances 0.000 description 6
- 229920005669 high impact polystyrene Polymers 0.000 description 6
- 239000004700 high-density polyethylene Substances 0.000 description 6
- 239000004797 high-impact polystyrene Substances 0.000 description 6
- 239000012796 inorganic flame retardant Substances 0.000 description 6
- QUAMTGJKVDWJEQ-UHFFFAOYSA-N octabenzone Chemical compound OC1=CC(OCCCCCCCC)=CC=C1C(=O)C1=CC=CC=C1 QUAMTGJKVDWJEQ-UHFFFAOYSA-N 0.000 description 6
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 6
- 239000004800 polyvinyl chloride Substances 0.000 description 6
- JIHQDMXYYFUGFV-UHFFFAOYSA-N 1,3,5-triazine Chemical group C1=NC=NC=N1 JIHQDMXYYFUGFV-UHFFFAOYSA-N 0.000 description 5
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 5
- JKIJEFPNVSHHEI-UHFFFAOYSA-N Phenol, 2,4-bis(1,1-dimethylethyl)-, phosphite (3:1) Chemical compound CC(C)(C)C1=CC(C(C)(C)C)=CC=C1OP(OC=1C(=CC(=CC=1)C(C)(C)C)C(C)(C)C)OC1=CC=C(C(C)(C)C)C=C1C(C)(C)C JKIJEFPNVSHHEI-UHFFFAOYSA-N 0.000 description 5
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical compound OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 description 5
- 125000002723 alicyclic group Chemical group 0.000 description 5
- 229910000410 antimony oxide Inorganic materials 0.000 description 5
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 5
- 229920001903 high density polyethylene Polymers 0.000 description 5
- 238000002347 injection Methods 0.000 description 5
- 239000007924 injection Substances 0.000 description 5
- 238000002156 mixing Methods 0.000 description 5
- VTRUBDSFZJNXHI-UHFFFAOYSA-N oxoantimony Chemical compound [Sb]=O VTRUBDSFZJNXHI-UHFFFAOYSA-N 0.000 description 5
- 229920000728 polyester Polymers 0.000 description 5
- 229920000915 polyvinyl chloride Polymers 0.000 description 5
- BHYQWBKCXBXPKM-UHFFFAOYSA-N tris[3-bromo-2,2-bis(bromomethyl)propyl] phosphate Chemical compound BrCC(CBr)(CBr)COP(=O)(OCC(CBr)(CBr)CBr)OCC(CBr)(CBr)CBr BHYQWBKCXBXPKM-UHFFFAOYSA-N 0.000 description 5
- KJYSXRBJOSZLEL-UHFFFAOYSA-N (2,4-ditert-butylphenyl) 3,5-ditert-butyl-4-hydroxybenzoate Chemical compound CC(C)(C)C1=CC(C(C)(C)C)=CC=C1OC(=O)C1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 KJYSXRBJOSZLEL-UHFFFAOYSA-N 0.000 description 4
- OLFNXLXEGXRUOI-UHFFFAOYSA-N 2-(benzotriazol-2-yl)-4,6-bis(2-phenylpropan-2-yl)phenol Chemical compound C=1C(N2N=C3C=CC=CC3=N2)=C(O)C(C(C)(C)C=2C=CC=CC=2)=CC=1C(C)(C)C1=CC=CC=C1 OLFNXLXEGXRUOI-UHFFFAOYSA-N 0.000 description 4
- UZUNCLSDTUBVCN-UHFFFAOYSA-N 2-(benzotriazol-2-yl)-6-(2-phenylpropan-2-yl)-4-(2,4,4-trimethylpentan-2-yl)phenol Chemical compound C=1C(C(C)(C)CC(C)(C)C)=CC(N2N=C3C=CC=CC3=N2)=C(O)C=1C(C)(C)C1=CC=CC=C1 UZUNCLSDTUBVCN-UHFFFAOYSA-N 0.000 description 4
- VVISQEKWYPFFLK-UHFFFAOYSA-N 2-n,2-n,4-n,4-n-tetrabutyl-6-chloro-1,3,5-triazine-2,4-diamine Chemical compound CCCCN(CCCC)C1=NC(Cl)=NC(N(CCCC)CCCC)=N1 VVISQEKWYPFFLK-UHFFFAOYSA-N 0.000 description 4
- UWSMKYBKUPAEJQ-UHFFFAOYSA-N 5-Chloro-2-(3,5-di-tert-butyl-2-hydroxyphenyl)-2H-benzotriazole Chemical compound CC(C)(C)C1=CC(C(C)(C)C)=CC(N2N=C3C=C(Cl)C=CC3=N2)=C1O UWSMKYBKUPAEJQ-UHFFFAOYSA-N 0.000 description 4
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 4
- 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 4
- MTAZNLWOLGHBHU-UHFFFAOYSA-N butadiene-styrene rubber Chemical compound C=CC=C.C=CC1=CC=CC=C1 MTAZNLWOLGHBHU-UHFFFAOYSA-N 0.000 description 4
- 239000003054 catalyst Substances 0.000 description 4
- 239000007859 condensation product Substances 0.000 description 4
- 239000000446 fuel Substances 0.000 description 4
- 150000004820 halides Chemical class 0.000 description 4
- 125000001624 naphthyl group Chemical group 0.000 description 4
- 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 4
- 229920002959 polymer blend Polymers 0.000 description 4
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 4
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 4
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 4
- WOFYQUJNULCFLN-UHFFFAOYSA-N saytex bn 451 Chemical compound BrC1C(Br)C2CC1C(C1=O)C2C(=O)N1CCN(C1=O)C(=O)C2C1C1CC2C(Br)C1Br WOFYQUJNULCFLN-UHFFFAOYSA-N 0.000 description 4
- 239000003381 stabilizer Substances 0.000 description 4
- KAKZBPTYRLMSJV-UHFFFAOYSA-N vinyl-ethylene Natural products C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 4
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 3
- SCSMZMBYJMIJTK-UHFFFAOYSA-N 2,4,9,10,11-pentaoxa-5,8-diaza-1lambda5,3lambda5-diphosphatricyclo[6.1.1.13,5]undecane 1,3-dioxide Chemical compound O1P(=O)(O2)ON2CCN2OP1(=O)O2 SCSMZMBYJMIJTK-UHFFFAOYSA-N 0.000 description 3
- ZMWRRFHBXARRRT-UHFFFAOYSA-N 2-(benzotriazol-2-yl)-4,6-bis(2-methylbutan-2-yl)phenol Chemical compound CCC(C)(C)C1=CC(C(C)(C)CC)=CC(N2N=C3C=CC=CC3=N2)=C1O ZMWRRFHBXARRRT-UHFFFAOYSA-N 0.000 description 3
- YZXTWMQYSSMUFH-UHFFFAOYSA-N 4-[6-(1-amino-2,2,6,6-tetramethylpiperidin-4-yl)hexyl]-2,2,6,6-tetramethylpiperidin-1-amine Chemical compound C1C(C)(C)N(N)C(C)(C)CC1CCCCCCC1CC(C)(C)N(N)C(C)(C)C1 YZXTWMQYSSMUFH-UHFFFAOYSA-N 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- 239000004716 Ethylene/acrylic acid copolymer Substances 0.000 description 3
- 229920010126 Linear Low Density Polyethylene (LLDPE) Polymers 0.000 description 3
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- 125000005262 alkoxyamine group Chemical group 0.000 description 3
- 125000005250 alkyl acrylate group Chemical group 0.000 description 3
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 3
- 125000000732 arylene group Chemical group 0.000 description 3
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 3
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 description 3
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 3
- ZEFSGHVBJCEKAZ-UHFFFAOYSA-N bis(2,4-ditert-butyl-6-methylphenyl) ethyl phosphite Chemical compound CC=1C=C(C(C)(C)C)C=C(C(C)(C)C)C=1OP(OCC)OC1=C(C)C=C(C(C)(C)C)C=C1C(C)(C)C ZEFSGHVBJCEKAZ-UHFFFAOYSA-N 0.000 description 3
- CJZGTCYPCWQAJB-UHFFFAOYSA-L calcium stearate Chemical compound [Ca+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CJZGTCYPCWQAJB-UHFFFAOYSA-L 0.000 description 3
- 125000001589 carboacyl group Chemical group 0.000 description 3
- 229910002091 carbon monoxide Inorganic materials 0.000 description 3
- 239000003610 charcoal Substances 0.000 description 3
- 238000009841 combustion method Methods 0.000 description 3
- 238000009833 condensation Methods 0.000 description 3
- 230000005494 condensation Effects 0.000 description 3
- 238000004786 cone calorimetry Methods 0.000 description 3
- ZJIPHXXDPROMEF-UHFFFAOYSA-N dihydroxyphosphanyl dihydrogen phosphite Chemical compound OP(O)OP(O)O ZJIPHXXDPROMEF-UHFFFAOYSA-N 0.000 description 3
- MCPKSFINULVDNX-UHFFFAOYSA-N drometrizole Chemical compound CC1=CC=C(O)C(N2N=C3C=CC=CC3=N2)=C1 MCPKSFINULVDNX-UHFFFAOYSA-N 0.000 description 3
- 229920001971 elastomer Polymers 0.000 description 3
- HQQADJVZYDDRJT-UHFFFAOYSA-N ethene;prop-1-ene Chemical group C=C.CC=C HQQADJVZYDDRJT-UHFFFAOYSA-N 0.000 description 3
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 3
- 238000001125 extrusion Methods 0.000 description 3
- 125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 description 3
- 229910052736 halogen Inorganic materials 0.000 description 3
- 150000002367 halogens Chemical class 0.000 description 3
- 229910001385 heavy metal Inorganic materials 0.000 description 3
- 238000001746 injection moulding Methods 0.000 description 3
- 150000005673 monoalkenes Chemical class 0.000 description 3
- 229910052760 oxygen Inorganic materials 0.000 description 3
- 239000001301 oxygen Substances 0.000 description 3
- 125000003884 phenylalkyl group Chemical group 0.000 description 3
- UEZVMMHDMIWARA-UHFFFAOYSA-M phosphonate Chemical compound [O-]P(=O)=O UEZVMMHDMIWARA-UHFFFAOYSA-M 0.000 description 3
- 238000006116 polymerization reaction Methods 0.000 description 3
- 150000003254 radicals Chemical class 0.000 description 3
- 239000005060 rubber Substances 0.000 description 3
- WGKLOLBTFWFKOD-UHFFFAOYSA-N tris(2-nonylphenyl) phosphite Chemical compound CCCCCCCCCC1=CC=CC=C1OP(OC=1C(=CC=CC=1)CCCCCCCCC)OC1=CC=CC=C1CCCCCCCCC WGKLOLBTFWFKOD-UHFFFAOYSA-N 0.000 description 3
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 3
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- 150000002013 dioxins Chemical class 0.000 description 1
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- RIZMRRKBZQXFOY-UHFFFAOYSA-N ethion Chemical compound CCOP(=S)(OCC)SCSP(=S)(OCC)OCC RIZMRRKBZQXFOY-UHFFFAOYSA-N 0.000 description 1
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- QQVIHTHCMHWDBS-UHFFFAOYSA-L isophthalate(2-) Chemical compound [O-]C(=O)C1=CC=CC(C([O-])=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-L 0.000 description 1
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- ZLNQQNXFFQJAID-UHFFFAOYSA-L magnesium carbonate Chemical compound [Mg+2].[O-]C([O-])=O ZLNQQNXFFQJAID-UHFFFAOYSA-L 0.000 description 1
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- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 1
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- 229910052919 magnesium silicate Inorganic materials 0.000 description 1
- 235000019792 magnesium silicate Nutrition 0.000 description 1
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 1
- 239000006078 metal deactivator Substances 0.000 description 1
- 229910052987 metal hydride Inorganic materials 0.000 description 1
- 150000004681 metal hydrides Chemical class 0.000 description 1
- 239000012968 metallocene catalyst Substances 0.000 description 1
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 description 1
- ZGEGCLOFRBLKSE-UHFFFAOYSA-N methylene hexane Natural products CCCCCC=C ZGEGCLOFRBLKSE-UHFFFAOYSA-N 0.000 description 1
- BAQLUVXNKOTTHU-UHFFFAOYSA-N metofenazate Chemical compound COC1=C(OC)C(OC)=CC(C(=O)OCCN2CCN(CCCN3C4=CC(Cl)=CC=C4SC4=CC=CC=C43)CC2)=C1 BAQLUVXNKOTTHU-UHFFFAOYSA-N 0.000 description 1
- 239000003607 modifier Substances 0.000 description 1
- KIWSYRHAAPLJFJ-DNZSEPECSA-N n-[(e,2z)-4-ethyl-2-hydroxyimino-5-nitrohex-3-enyl]pyridine-3-carboxamide Chemical compound [O-][N+](=O)C(C)C(/CC)=C/C(=N/O)/CNC(=O)C1=CC=CN=C1 KIWSYRHAAPLJFJ-DNZSEPECSA-N 0.000 description 1
- TVSPGDFLYLHCGW-MWBNKCOKSA-N n-[(e,2z)-4-ethyl-2-hydroxyimino-6-methyl-5-nitrohept-3-enyl]pyridine-3-carboxamide Chemical compound CC(C)C([N+]([O-])=O)C(/CC)=C/C(=N/O)/CNC(=O)C1=CC=CN=C1 TVSPGDFLYLHCGW-MWBNKCOKSA-N 0.000 description 1
- 125000001280 n-hexyl group Chemical group C(CCCCC)* 0.000 description 1
- LKPFBGKZCCBZDK-UHFFFAOYSA-N n-hydroxypiperidine Chemical compound ON1CCCCC1 LKPFBGKZCCBZDK-UHFFFAOYSA-N 0.000 description 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000001971 neopentyl group Chemical group [H]C([*])([H])C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- JFNLZVQOOSMTJK-KNVOCYPGSA-N norbornene Chemical compound C1[C@@H]2CC[C@H]1C=C2 JFNLZVQOOSMTJK-KNVOCYPGSA-N 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 239000011368 organic material Substances 0.000 description 1
- 150000002903 organophosphorus compounds Chemical class 0.000 description 1
- 235000006408 oxalic acid Nutrition 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 125000000466 oxiranyl group Chemical group 0.000 description 1
- FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 description 1
- 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 description 1
- XRBCRPZXSCBRTK-UHFFFAOYSA-N phosphonous acid Chemical class OPO XRBCRPZXSCBRTK-UHFFFAOYSA-N 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- XFZRQAZGUOTJCS-UHFFFAOYSA-N phosphoric acid;1,3,5-triazine-2,4,6-triamine Chemical compound OP(O)(O)=O.NC1=NC(N)=NC(N)=N1 XFZRQAZGUOTJCS-UHFFFAOYSA-N 0.000 description 1
- 150000003018 phosphorus compounds Chemical class 0.000 description 1
- XNGIFLGASWRNHJ-UHFFFAOYSA-L phthalate(2-) Chemical compound [O-]C(=O)C1=CC=CC=C1C([O-])=O XNGIFLGASWRNHJ-UHFFFAOYSA-L 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
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- 229920001084 poly(chloroprene) Polymers 0.000 description 1
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 1
- 229920003251 poly(α-methylstyrene) Polymers 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920005638 polyethylene monopolymer Polymers 0.000 description 1
- 229920000139 polyethylene terephthalate Polymers 0.000 description 1
- 239000005020 polyethylene terephthalate Substances 0.000 description 1
- 229920001195 polyisoprene Polymers 0.000 description 1
- 229920005606 polypropylene copolymer Polymers 0.000 description 1
- 229920002620 polyvinyl fluoride Polymers 0.000 description 1
- 239000005033 polyvinylidene chloride Substances 0.000 description 1
- 229920002981 polyvinylidene fluoride Polymers 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 238000010526 radical polymerization reaction Methods 0.000 description 1
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- 229960004889 salicylic acid Drugs 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
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- 238000012216 screening Methods 0.000 description 1
- 229940116351 sebacate Drugs 0.000 description 1
- CXMXRPHRNRROMY-UHFFFAOYSA-L sebacate(2-) Chemical compound [O-]C(=O)CCCCCCCCC([O-])=O CXMXRPHRNRROMY-UHFFFAOYSA-L 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 229910052814 silicon oxide Inorganic materials 0.000 description 1
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- 230000000087 stabilizing effect Effects 0.000 description 1
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- 125000001424 substituent group Chemical group 0.000 description 1
- 125000000446 sulfanediyl group Chemical group *S* 0.000 description 1
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- KJAMZCVTJDTESW-UHFFFAOYSA-N tiracizine Chemical compound C1CC2=CC=CC=C2N(C(=O)CN(C)C)C2=CC(NC(=O)OCC)=CC=C21 KJAMZCVTJDTESW-UHFFFAOYSA-N 0.000 description 1
- YONPGGFAJWQGJC-UHFFFAOYSA-K titanium(iii) chloride Chemical compound Cl[Ti](Cl)Cl YONPGGFAJWQGJC-UHFFFAOYSA-K 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- GBXQPDCOMJJCMJ-UHFFFAOYSA-M trimethyl-[6-(trimethylazaniumyl)hexyl]azanium;bromide Chemical compound [Br-].C[N+](C)(C)CCCCCC[N+](C)(C)C GBXQPDCOMJJCMJ-UHFFFAOYSA-M 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
- LENZDBCJOHFCAS-UHFFFAOYSA-N tris Chemical compound OCC(N)(CO)CO LENZDBCJOHFCAS-UHFFFAOYSA-N 0.000 description 1
- MGMXGCZJYUCMGY-UHFFFAOYSA-N tris(4-nonylphenyl) phosphite Chemical compound C1=CC(CCCCCCCCC)=CC=C1OP(OC=1C=CC(CCCCCCCCC)=CC=1)OC1=CC=C(CCCCCCCCC)C=C1 MGMXGCZJYUCMGY-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
- 150000003672 ureas Chemical group 0.000 description 1
- SPDZFJLQFWSJGA-UHFFFAOYSA-N uredepa Chemical compound C1CN1P(=O)(NC(=O)OCC)N1CC1 SPDZFJLQFWSJGA-UHFFFAOYSA-N 0.000 description 1
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- 125000006839 xylylene group Chemical group 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
- 239000004711 α-olefin 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
- C08K5/16—Nitrogen-containing compounds
- C08K5/34—Heterocyclic compounds having nitrogen in the ring
- C08K5/3467—Heterocyclic compounds having nitrogen in the ring having more than two nitrogen atoms in the ring
- C08K5/3477—Six-membered rings
- C08K5/3492—Triazines
- C08K5/34926—Triazines also containing heterocyclic groups other than triazine groups
-
- 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
- C08K5/16—Nitrogen-containing compounds
- C08K5/34—Heterocyclic compounds having nitrogen in the ring
- C08K5/3412—Heterocyclic compounds having nitrogen in the ring having one nitrogen atom in the ring
- C08K5/3432—Six-membered rings
- C08K5/3435—Piperidines
-
- 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
- C08K5/0008—Organic ingredients according to more than one of the "one dot" groups of C08K5/01 - C08K5/59
- C08K5/0066—Flame-proofing or flame-retarding additives
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Paper (AREA)
- Printing Methods (AREA)
- Hydrogenated Pyridines (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US5133197P | 1997-06-30 | 1997-06-30 | |
| US60/051,331 | 1997-06-30 | ||
| PCT/US1998/013469 WO1999000450A1 (en) | 1997-06-30 | 1998-06-25 | Flame retardant compositions |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| KR20010014333A KR20010014333A (ko) | 2001-02-26 |
| KR100540156B1 true KR100540156B1 (ko) | 2005-12-29 |
Family
ID=21970653
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR10-1999-7012483A Expired - Lifetime KR100540156B1 (ko) | 1997-06-30 | 1998-06-25 | 방염제 조성물 |
Country Status (12)
| Country | Link |
|---|---|
| EP (2) | EP1462481B1 (https=) |
| JP (1) | JP4378574B2 (https=) |
| KR (1) | KR100540156B1 (https=) |
| CN (1) | CN1178978C (https=) |
| AU (1) | AU735643B2 (https=) |
| BR (1) | BR9810957A (https=) |
| CA (1) | CA2292598C (https=) |
| DE (2) | DE69841728D1 (https=) |
| ES (1) | ES2227855T3 (https=) |
| RU (1) | RU2207352C2 (https=) |
| TW (1) | TW480276B (https=) |
| WO (1) | WO1999000450A1 (https=) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR101843220B1 (ko) * | 2011-03-31 | 2018-03-28 | 도레이 카부시키가이샤 | 탄소 섬유 강화 폴리프로필렌 수지 조성물, 성형 재료 및 성형품 |
Families Citing this family (85)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6309987B1 (en) * | 1998-04-20 | 2001-10-30 | Bba Nonwovens Simpsonville, Inc. | Nonwoven fabric having both UV stability and flame retardancy |
| EP1235863B1 (en) * | 1999-12-09 | 2005-01-26 | Ciba SC Holding AG | Use of an additive composition for increasing the storage stability of ethylenically unsaturated resins |
| JP2004083913A (ja) * | 2000-04-06 | 2004-03-18 | Mitsubishi Rayon Co Ltd | 難燃性ポリプロピレンフィルム |
| JP3540759B2 (ja) | 2000-04-06 | 2004-07-07 | 三菱レイヨン株式会社 | 難燃性ポリプロピレン繊維及びその製造方法 |
| JP3822046B2 (ja) * | 2000-10-11 | 2006-09-13 | 大和紡績株式会社 | 繊維およびその繊維組成物 |
| JP2002121333A (ja) * | 2000-10-13 | 2002-04-23 | Daiwabo Co Ltd | ポリオレフィン樹脂成形物及びそれからなるフィルム |
| TWI273115B (en) * | 2000-12-12 | 2007-02-11 | Ciba Sc Holding Ag | Improved weatherability of flame retardant polyolefin |
| GB2386901B (en) * | 2000-12-12 | 2004-03-31 | Ciba Sc Holding Ag | Improved weatherability of flame retardant polyolefin |
| JP2002322322A (ja) † | 2001-02-27 | 2002-11-08 | Bromine Compounds Ltd | 難燃性ポリオレフィン組成物 |
| DE60205734T2 (de) * | 2001-03-20 | 2006-03-09 | Ciba Speciality Chemicals Holding Inc. | Flammhemmende zusammensetzungen |
| US6465645B1 (en) | 2001-04-17 | 2002-10-15 | Ciba Specialty Chemicals Corporation | Long chain hindered amines and compositions stabilized therewith |
| JP3679738B2 (ja) * | 2001-07-16 | 2005-08-03 | 三菱レイヨン株式会社 | 難燃性ポリプロピレン繊維及びその製造方法 |
| US6822023B2 (en) * | 2001-12-03 | 2004-11-23 | Kaneka Corporation | Flame retardant polyolefin resin pre-expanded particles and in-mold foamed articles prepared therefrom |
| CN1602334A (zh) * | 2001-12-10 | 2005-03-30 | 西巴特殊化学品控股有限公司 | 阻燃剂组合物 |
| KR101029863B1 (ko) | 2001-12-21 | 2011-04-18 | 시바 홀딩 인코포레이티드 | 신규한 난연제 화합물 |
| JP2003251771A (ja) * | 2002-02-28 | 2003-09-09 | Hagihara Industries Inc | ポリオレフィン防炎性ラミネートシート |
| JP4091317B2 (ja) * | 2002-02-28 | 2008-05-28 | 萩原工業株式会社 | 光透過性を有するクロスシート |
| JP2004315544A (ja) * | 2002-02-28 | 2004-11-11 | Hagihara Industries Inc | ポリオレフィンフイルムまたはラミネートシート |
| JP2003251748A (ja) * | 2002-02-28 | 2003-09-09 | Hagihara Industries Inc | 膜材料ラミネートシート |
| JP2003251767A (ja) * | 2002-02-28 | 2003-09-09 | Hagihara Industries Inc | 不織布補強用ポリオレフィンクロスシート |
| JP4009117B2 (ja) * | 2002-03-06 | 2007-11-14 | 大和紡績株式会社 | オレフィン複合シートおよび強化複合不織布 |
| US7323502B2 (en) * | 2002-03-12 | 2008-01-29 | Ciba Specialty Chemicals Corporation | Flame retardant compositions |
| JP2004000173A (ja) * | 2002-03-28 | 2004-01-08 | Hagihara Industries Inc | 防草シート |
| JP3895207B2 (ja) * | 2002-03-29 | 2007-03-22 | 大和紡績株式会社 | 難燃性ポリオレフィン繊維およびこれを用いた繊維組成物と繊維積層体 |
| CA2479946A1 (en) * | 2002-04-10 | 2003-10-16 | Ciba Specialty Chemicals Holding Inc. | Flame retardant coatings |
| JP4324940B2 (ja) * | 2002-04-17 | 2009-09-02 | チバ ホールディング インコーポレーテッド | ヒドロキシルアミンエステル含有難燃性ポリマー組成物 |
| JP2003313737A (ja) * | 2002-04-24 | 2003-11-06 | Hagihara Industries Inc | パイル糸 |
| JP2004019074A (ja) * | 2002-06-19 | 2004-01-22 | Hagihara Industries Inc | 防虫網 |
| JP4016123B2 (ja) * | 2002-07-22 | 2007-12-05 | 平岡織染株式会社 | 難燃化ポリプロピレン系樹脂膜材 |
| JP2006501340A (ja) * | 2002-10-03 | 2006-01-12 | チバ スペシャルティ ケミカルズ ホールディング インコーポレーテッド | 難燃性組成物 |
| JP2004131869A (ja) * | 2002-10-10 | 2004-04-30 | Mitsubishi Rayon Co Ltd | 難燃性を有するポリプロピレン系熱接着性複合繊維及びその製造方法 |
| MY139230A (en) * | 2002-10-17 | 2009-08-28 | Ciba Holding Inc | Flame retardant polymeric electrical parts |
| US7109260B2 (en) * | 2002-10-17 | 2006-09-19 | Ciba Specialty Chemicals Corporation | Flame retardant compositions |
| CN100352852C (zh) * | 2002-10-17 | 2007-12-05 | 西巴特殊化学品控股有限公司 | 阻燃聚合物电气部件 |
| US7138448B2 (en) * | 2002-11-04 | 2006-11-21 | Ciba Specialty Chemicals Corporation | Flame retardant compositions |
| JP2004161850A (ja) * | 2002-11-12 | 2004-06-10 | Mitsubishi Rayon Co Ltd | 難燃性シート状物 |
| JP4077745B2 (ja) * | 2003-02-28 | 2008-04-23 | 株式会社ジェイエスピー | ポリオレフィン系樹脂型内発泡成形体 |
| JP4158559B2 (ja) * | 2003-03-07 | 2008-10-01 | 東洋インキ製造株式会社 | 難燃性樹脂組成物およびそれを用いたシート |
| DE102004018845B4 (de) | 2003-04-25 | 2018-06-21 | Chisso Polypro Fiber Co., Ltd | Flammfeste Faser und Faserformteil, bei dem die flammfeste Faser verwendet wird |
| JP3879695B2 (ja) * | 2003-04-25 | 2007-02-14 | チッソ株式会社 | 難燃性ポリオレフィン樹脂組成物 |
| CN100500744C (zh) * | 2003-07-18 | 2009-06-17 | 西巴特殊化学品控股有限公司 | 阻燃性聚乳酸 |
| WO2006070859A1 (ja) * | 2004-12-28 | 2006-07-06 | Mitsubishi Rayon Co., Ltd. | ポリプロピレン難燃繊維およびこれを用いた織編物並びに繊維製品 |
| JP2006316168A (ja) * | 2005-05-12 | 2006-11-24 | Marubishi Oil Chem Co Ltd | 難燃剤及びそれを含む合成樹脂組成物 |
| JP4721823B2 (ja) * | 2005-08-23 | 2011-07-13 | 出光ライオンコンポジット株式会社 | 難燃性樹脂組成物及びそれからなる成形体 |
| US20090318592A1 (en) * | 2005-10-11 | 2009-12-24 | Ciba Corporation | Process for the Synthesis of Amine Ethers |
| JP5420911B2 (ja) | 2006-03-16 | 2014-02-19 | クラリアント ファイナンス (ビーブイアイ) リミティド | 変性ロウ、それらの製造方法及びそれらの使用 |
| CN101405306B (zh) * | 2006-03-16 | 2011-07-27 | 克莱里安特财务(Bvi)有限公司 | 改性蜡、其制备方法及其用途 |
| CN101631774B (zh) * | 2007-02-21 | 2012-07-18 | 巴斯夫欧洲公司 | 阻燃组合物中合成的对称偶氮化合物 |
| ATE541889T1 (de) | 2008-09-05 | 2012-02-15 | Thor Gmbh | Flammschutzzusammensetzung enthaltend ein phosphonsäurederivat |
| JP5690265B2 (ja) * | 2009-04-15 | 2015-03-25 | 株式会社カネカ | ポリオレフィン系樹脂予備発泡粒子およびポリオレフィン系樹脂予備発泡粒子からなるポリオレフィン系樹脂型内発泡成形体 |
| JP2011068717A (ja) * | 2009-09-24 | 2011-04-07 | Yazaki Corp | 難燃性樹脂組成物 |
| CN102712668A (zh) | 2010-01-15 | 2012-10-03 | 巴斯夫欧洲公司 | 经磷取代的烷氧胺化合物 |
| CN102834445A (zh) * | 2010-03-25 | 2012-12-19 | 巴斯夫欧洲公司 | 次膦酸盐和硝酰基衍生物的阻燃剂组合物 |
| JP5581133B2 (ja) * | 2010-07-02 | 2014-08-27 | 日本ポリエチレン株式会社 | 太陽電池封止材用樹脂組成物、及びそれを用いた太陽電池封止材、その製造方法、ならびに太陽電池モジュール |
| CN103025812B (zh) * | 2010-07-28 | 2014-08-13 | 巴斯夫欧洲公司 | 次膦酰肼阻燃组合物 |
| WO2012013565A1 (en) | 2010-07-29 | 2012-02-02 | Basf Se | Phosphinic acid hydrazide flame retardant compositions |
| CN101914217B (zh) * | 2010-07-29 | 2011-12-28 | 济南泰星精细化工有限公司 | 一种替代三氧化二锑的环保阻燃剂 |
| JP6188734B2 (ja) | 2012-03-16 | 2017-08-30 | ビーエーエスエフ ソシエタス・ヨーロピアBasf Se | 難燃剤としてのnor−hals化合物 |
| JP2014062189A (ja) * | 2012-09-21 | 2014-04-10 | Mitsubishi Motors Corp | 車輌用バッテリーケース |
| DE102012022482A1 (de) | 2012-11-19 | 2014-05-22 | Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. | Polymerzusammensetzung mit verbesserter Langzeitstabilität, hieraus hergestellte Formteile sowie Verwendungszwecke |
| DE102013005307A1 (de) | 2013-03-25 | 2014-09-25 | Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. | Verwendung von organischen Oxyimiden als Flammschutzmittel für Kunststoffe sowie flammgeschützte Kunststoffzusammensetzung und hieraus hergestelltem Formteil |
| DE102013012487A1 (de) | 2013-07-26 | 2015-01-29 | Clariant International Ltd. | Zusammensetzung aus einem thermoplastischen Polymer und einer synergistischen Mischung aus bestimmten Aminoethern und feinteiligen Phosphinaten |
| EP2871208A1 (en) | 2013-11-08 | 2015-05-13 | Carl-Eric Wilen | Sulfenamides, sulfinamides and sulfonamides as flame retardants |
| DE102014210214A1 (de) | 2014-05-28 | 2015-12-03 | Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. | Verwendung von Oxyimid-enthaltenden Copolymeren oder Polymeren als Flammschutzmittel, Stabilisatoren, Rheologiemodifikatoren für Kunststoffe, Initiatoren für Polymerisations- und Pfropfprozesse, Vernetzungs- oder Kopplungsmittel sowie solche Copolymere oder Polymere enthaltende Kunststoffformmassen |
| DE102014211276A1 (de) | 2014-06-12 | 2015-12-17 | Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. | Verwendung von Hydroxybenzotriazol-Derivaten und/oder Hydroxy-Indazol-Derivaten als Flammschutzmittel für Kunststoffe sowie flammgeschützte Kunststoffformmasse |
| ES2743478T3 (es) | 2014-06-24 | 2020-02-19 | Dow Global Technologies Llc | Lámina posterior fotovoltaica de poliolefina que comprende una capa de polipropileno estabilizado |
| DE102014218811A1 (de) | 2014-09-18 | 2016-03-24 | Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. | Verwendung von phosphorhaltigen organischen Oxyimiden als Flammschutzmittel, Radikalgeneratoren und/oder als Stabilisatoren für Kunststoffe, flammgeschützte Kunststoffzusammensetzung, Verfahren zu deren Herstellung sowie Formteile, Lacke und Beschichtungen |
| DE102014218810B3 (de) | 2014-09-18 | 2016-01-28 | Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. | Verwendung von organischen Oxyimidsalzen als Flammschutzmittel, flammengeschützte Kunststoffzusammensetzung, Verfahren zur ihrer Herstellung sowie Formteil, Lack oder Beschichtung |
| MX2018000885A (es) * | 2015-07-20 | 2018-05-15 | Basf Se | Sistemas de poliolefina retardantes de llama. |
| JP6826846B2 (ja) * | 2016-09-13 | 2021-02-10 | 日本ポリエチレン株式会社 | 難燃性フィルム |
| TW201930570A (zh) | 2017-11-13 | 2019-08-01 | 瑞士商科萊恩塑料和塗料公司 | 用於聚烯烴之新穎阻燃劑組成物 |
| JP7241513B2 (ja) * | 2018-11-20 | 2023-03-17 | Psジャパン株式会社 | 難燃性スチレン系樹脂組成物、及び成形品 |
| CN109524162B (zh) * | 2018-11-23 | 2019-06-18 | 廊坊江海洋线缆有限公司 | 一种超高阻燃耐候性电缆 |
| EP3891211A1 (en) | 2018-12-03 | 2021-10-13 | Italmatch Chemicals S.p.A. | Polyolefins halogen-free flame retardant moulding compositions comprising an inorganic hypophosphorous acid metal salt |
| JP7264649B2 (ja) * | 2019-01-21 | 2023-04-25 | Psジャパン株式会社 | 難燃性押出シート |
| JP7264650B2 (ja) * | 2019-01-21 | 2023-04-25 | Psジャパン株式会社 | 難燃性発泡体 |
| JP7219645B2 (ja) * | 2019-03-20 | 2023-02-08 | Psジャパン株式会社 | 難燃性スチレン系樹脂組成物、成形品、及び押出シート |
| CN112126060B (zh) * | 2019-06-25 | 2022-05-31 | 北京天罡助剂有限责任公司 | 一种聚合型高分子空间位阻胺及其制备方法 |
| CN111040293B (zh) * | 2019-12-17 | 2022-03-08 | 广东省石油与精细化工研究院 | 一种膨胀阻燃聚丙烯及其制备方法 |
| CN118599234A (zh) | 2020-02-21 | 2024-09-06 | Ps日本株式会社 | 苯乙烯类树脂组合物、阻燃性苯乙烯类树脂组合物和成型体以及贴片天线 |
| JP7729077B2 (ja) * | 2021-06-08 | 2025-08-26 | コニカミノルタ株式会社 | 樹脂組成物及びその製造方法 |
| CN113881153B (zh) * | 2021-09-24 | 2024-03-15 | 江苏金发科技新材料有限公司 | 一种透明无卤阻燃母粒及其制备方法和应用 |
| EP4365225A1 (en) | 2022-11-04 | 2024-05-08 | Clariant International Ltd | Flame-retardant composition, polymer composition comprising same and use thereof |
| JP2024149247A (ja) * | 2023-04-07 | 2024-10-18 | 出光ファインコンポジット株式会社 | 樹脂組成物 |
| WO2026033164A1 (en) | 2024-08-06 | 2026-02-12 | Idipsum Oy | Compounds, polymers, compositions and uses thereof, methods for preparing the compounds, the polymers, and molding compounds, and molding compounds obtainable by the methods |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4978699A (en) * | 1988-10-24 | 1990-12-18 | Atochem North America, Inc. | Light stabilizing flame retardants |
| US5393812A (en) * | 1993-08-31 | 1995-02-28 | Hercules Incorporated | Flame retardant, light stable composition |
| EP0792911A3 (en) * | 1996-02-27 | 1998-01-14 | Fmc Corporation | Flame resistant polyolefin compositions |
-
1998
- 1998-06-25 BR BR9810957-0A patent/BR9810957A/pt not_active IP Right Cessation
- 1998-06-25 WO PCT/US1998/013469 patent/WO1999000450A1/en not_active Ceased
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- 1998-06-25 KR KR10-1999-7012483A patent/KR100540156B1/ko not_active Expired - Lifetime
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- 1998-06-25 RU RU2000102671/04A patent/RU2207352C2/ru active
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Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR101843220B1 (ko) * | 2011-03-31 | 2018-03-28 | 도레이 카부시키가이샤 | 탄소 섬유 강화 폴리프로필렌 수지 조성물, 성형 재료 및 성형품 |
Also Published As
| Publication number | Publication date |
|---|---|
| WO1999000450A1 (en) | 1999-01-07 |
| EP1462481B1 (en) | 2010-06-16 |
| DE69826477T2 (de) | 2005-11-17 |
| EP1462481A3 (en) | 2004-10-13 |
| CA2292598A1 (en) | 1999-01-07 |
| DE69826477D1 (de) | 2004-10-28 |
| DE69841728D1 (de) | 2010-07-29 |
| CN1261904A (zh) | 2000-08-02 |
| AU8174998A (en) | 1999-01-19 |
| AU735643B2 (en) | 2001-07-12 |
| RU2207352C2 (ru) | 2003-06-27 |
| EP0996669B1 (en) | 2004-09-22 |
| CA2292598C (en) | 2008-03-18 |
| EP0996669A1 (en) | 2000-05-03 |
| ES2227855T3 (es) | 2005-04-01 |
| JP2002507238A (ja) | 2002-03-05 |
| JP4378574B2 (ja) | 2009-12-09 |
| TW480276B (en) | 2002-03-21 |
| EP1462481A2 (en) | 2004-09-29 |
| CN1178978C (zh) | 2004-12-08 |
| BR9810957A (pt) | 2000-09-26 |
| KR20010014333A (ko) | 2001-02-26 |
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