AU665442B2 - Flame-retardant plastics molding composition of improved stability - Google Patents
Flame-retardant plastics molding composition of improved stability Download PDFInfo
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- AU665442B2 AU665442B2 AU44285/93A AU4428593A AU665442B2 AU 665442 B2 AU665442 B2 AU 665442B2 AU 44285/93 A AU44285/93 A AU 44285/93A AU 4428593 A AU4428593 A AU 4428593A AU 665442 B2 AU665442 B2 AU 665442B2
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- Australia
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- flame
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- 239000000203 mixture Substances 0.000 title claims abstract description 59
- 238000000465 moulding Methods 0.000 title claims abstract description 35
- 229920003023 plastic Polymers 0.000 title claims abstract description 17
- 239000004033 plastic Substances 0.000 title claims abstract description 17
- 239000003063 flame retardant Substances 0.000 title claims abstract description 15
- 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 14
- 239000002253 acid Substances 0.000 claims abstract description 21
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- 239000004114 Ammonium polyphosphate Substances 0.000 claims abstract description 13
- 235000019826 ammonium polyphosphate Nutrition 0.000 claims abstract description 13
- 229920001276 ammonium polyphosphate Polymers 0.000 claims abstract description 13
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- 125000003118 aryl group Chemical group 0.000 claims abstract description 6
- 239000000470 constituent Substances 0.000 claims abstract description 6
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- 229920000642 polymer Polymers 0.000 claims description 17
- 150000001875 compounds Chemical class 0.000 claims description 9
- 239000004743 Polypropylene Substances 0.000 claims description 7
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- 239000004698 Polyethylene Substances 0.000 claims description 4
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- 238000000034 method Methods 0.000 claims description 4
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- 238000002360 preparation method Methods 0.000 claims description 2
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- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 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 3
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- 230000000694 effects Effects 0.000 description 3
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- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
- 229920001897 terpolymer Polymers 0.000 description 3
- YHMYGUUIMTVXNW-UHFFFAOYSA-N 1,3-dihydrobenzimidazole-2-thione Chemical compound C1=CC=C2NC(S)=NC2=C1 YHMYGUUIMTVXNW-UHFFFAOYSA-N 0.000 description 2
- LNETULKMXZVUST-UHFFFAOYSA-N 1-naphthoic acid Chemical compound C1=CC=C2C(C(=O)O)=CC=CC2=C1 LNETULKMXZVUST-UHFFFAOYSA-N 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 description 2
- 229920002367 Polyisobutene Polymers 0.000 description 2
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 2
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 2
- UKMSUNONTOPOIO-UHFFFAOYSA-M behenate Chemical compound CCCCCCCCCCCCCCCCCCCCCC([O-])=O UKMSUNONTOPOIO-UHFFFAOYSA-M 0.000 description 2
- 229940116224 behenate Drugs 0.000 description 2
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 2
- 239000007859 condensation product Substances 0.000 description 2
- LPIQUOYDBNQMRZ-UHFFFAOYSA-N cyclopentene Chemical compound C1CC=CC1 LPIQUOYDBNQMRZ-UHFFFAOYSA-N 0.000 description 2
- XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 description 2
- 150000004679 hydroxides Chemical class 0.000 description 2
- 238000010348 incorporation Methods 0.000 description 2
- 238000001746 injection moulding Methods 0.000 description 2
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 2
- 239000003446 ligand Substances 0.000 description 2
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- IXHMTDIIQNIVBN-UHFFFAOYSA-N n'-(2,2-dihydroxyethyl)oxamide Chemical compound NC(=O)C(=O)NCC(O)O IXHMTDIIQNIVBN-UHFFFAOYSA-N 0.000 description 2
- 229910052759 nickel Inorganic materials 0.000 description 2
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 2
- ZQBAKBUEJOMQEX-UHFFFAOYSA-N phenyl salicylate Chemical compound OC1=CC=CC=C1C(=O)OC1=CC=CC=C1 ZQBAKBUEJOMQEX-UHFFFAOYSA-N 0.000 description 2
- AQSJGOWTSHOLKH-UHFFFAOYSA-N phosphite(3-) Chemical class [O-]P([O-])[O-] AQSJGOWTSHOLKH-UHFFFAOYSA-N 0.000 description 2
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- YODZTKMDCQEPHD-UHFFFAOYSA-N thiodiglycol Chemical compound OCCSCCO YODZTKMDCQEPHD-UHFFFAOYSA-N 0.000 description 2
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- 229920002554 vinyl polymer Polymers 0.000 description 2
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- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
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- NHDLVKOYPQPGNT-UHFFFAOYSA-N benzene-1,2,3,5-tetracarboxylic acid Chemical compound OC(=O)C1=CC(C(O)=O)=C(C(O)=O)C(C(O)=O)=C1 NHDLVKOYPQPGNT-UHFFFAOYSA-N 0.000 description 1
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- YWDBZVIHZORXHG-UHFFFAOYSA-N bis(2,2,6,6-tetramethylpiperidin-1-yl) decanedioate Chemical compound CC1(C)CCCC(C)(C)N1OC(=O)CCCCCCCCC(=O)ON1C(C)(C)CCCC1(C)C YWDBZVIHZORXHG-UHFFFAOYSA-N 0.000 description 1
- 229920001400 block copolymer Polymers 0.000 description 1
- KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
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- 238000004132 cross linking Methods 0.000 description 1
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- MNNHAPBLZZVQHP-UHFFFAOYSA-N diammonium hydrogen phosphate Chemical compound [NH4+].[NH4+].OP([O-])([O-])=O MNNHAPBLZZVQHP-UHFFFAOYSA-N 0.000 description 1
- 229940087101 dibenzylidene sorbitol Drugs 0.000 description 1
- 150000001991 dicarboxylic acids Chemical class 0.000 description 1
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- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 239000000539 dimer Substances 0.000 description 1
- UHDWKEMHZPZGFY-UHFFFAOYSA-N dispiro[5.1.11^{8}.2^{6}]henicosan-5-one Chemical compound O=C1CCCCC11CC2(CCCCCCCCCCC2)CC1 UHDWKEMHZPZGFY-UHFFFAOYSA-N 0.000 description 1
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- SUPCQIBBMFXVTL-UHFFFAOYSA-N ethyl 2-methylprop-2-enoate Chemical compound CCOC(=O)C(C)=C SUPCQIBBMFXVTL-UHFFFAOYSA-N 0.000 description 1
- 125000004494 ethyl ester group Chemical group 0.000 description 1
- VXNZUUAINFGPBY-UHFFFAOYSA-N ethyl ethylene Natural products CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
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- 238000001704 evaporation Methods 0.000 description 1
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- 229930195729 fatty acid Natural products 0.000 description 1
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- 239000000835 fiber Substances 0.000 description 1
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- WOLATMHLPFJRGC-UHFFFAOYSA-N furan-2,5-dione;styrene Chemical compound O=C1OC(=O)C=C1.C=CC1=CC=CC=C1 WOLATMHLPFJRGC-UHFFFAOYSA-N 0.000 description 1
- 239000003365 glass fiber Substances 0.000 description 1
- 229920000578 graft copolymer Polymers 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 239000010439 graphite Substances 0.000 description 1
- 229910002804 graphite Inorganic materials 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- AHAREKHAZNPPMI-UHFFFAOYSA-N hexa-1,3-diene Chemical compound CCC=CC=C AHAREKHAZNPPMI-UHFFFAOYSA-N 0.000 description 1
- IPCSVZSSVZVIGE-UHFFFAOYSA-M hexadecanoate Chemical compound CCCCCCCCCCCCCCCC([O-])=O IPCSVZSSVZVIGE-UHFFFAOYSA-M 0.000 description 1
- 150000002429 hydrazines Chemical class 0.000 description 1
- 125000002768 hydroxyalkyl group Chemical group 0.000 description 1
- 229920000554 ionomer Polymers 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 239000004611 light stabiliser Substances 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 1
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- 239000000178 monomer Substances 0.000 description 1
- 125000001421 myristyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- YIMHRDBSVCPJOV-UHFFFAOYSA-N n'-(2-ethoxyphenyl)-n-(2-ethylphenyl)oxamide Chemical compound CCOC1=CC=CC=C1NC(=O)C(=O)NC1=CC=CC=C1CC YIMHRDBSVCPJOV-UHFFFAOYSA-N 0.000 description 1
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 1
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- MGFYIUFZLHCRTH-UHFFFAOYSA-N nitrilotriacetic acid Chemical compound OC(=O)CN(CC(O)=O)CC(O)=O MGFYIUFZLHCRTH-UHFFFAOYSA-N 0.000 description 1
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- 125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- GUSFEBGYPWJUSS-UHFFFAOYSA-N pentaazanium;[oxido(phosphonatooxy)phosphoryl] phosphate Chemical compound [NH4+].[NH4+].[NH4+].[NH4+].[NH4+].[O-]P([O-])(=O)OP([O-])(=O)OP([O-])([O-])=O GUSFEBGYPWJUSS-UHFFFAOYSA-N 0.000 description 1
- RGSFGYAAUTVSQA-UHFFFAOYSA-N pentamethylene Natural products C1CCCC1 RGSFGYAAUTVSQA-UHFFFAOYSA-N 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
- 150000002978 peroxides Chemical class 0.000 description 1
- 150000004707 phenolate Chemical class 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 229960000969 phenyl salicylate Drugs 0.000 description 1
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 1
- XRBCRPZXSCBRTK-UHFFFAOYSA-N phosphonous acid Chemical class OPO XRBCRPZXSCBRTK-UHFFFAOYSA-N 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 125000005936 piperidyl group Chemical group 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
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- 235000011176 polyphosphates Nutrition 0.000 description 1
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- WBHHMMIMDMUBKC-QJWNTBNXSA-M ricinoleate Chemical compound CCCCCC[C@@H](O)C\C=C/CCCCCCCC([O-])=O WBHHMMIMDMUBKC-QJWNTBNXSA-M 0.000 description 1
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- 150000004760 silicates Chemical class 0.000 description 1
- JMHCCAYJTTWMCX-QWPJCUCISA-M sodium;(2s)-2-amino-3-[4-(4-hydroxy-3,5-diiodophenoxy)-3,5-diiodophenyl]propanoate;pentahydrate Chemical compound O.O.O.O.O.[Na+].IC1=CC(C[C@H](N)C([O-])=O)=CC(I)=C1OC1=CC(I)=C(O)C(I)=C1 JMHCCAYJTTWMCX-QWPJCUCISA-M 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
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- 239000000454 talc Substances 0.000 description 1
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- IVIIAEVMQHEPAY-UHFFFAOYSA-N tridodecyl phosphite Chemical compound CCCCCCCCCCCCOP(OCCCCCCCCCCCC)OCCCCCCCCCCCC IVIIAEVMQHEPAY-UHFFFAOYSA-N 0.000 description 1
- 239000013638 trimer Substances 0.000 description 1
- CNUJLMSKURPSHE-UHFFFAOYSA-N trioctadecyl phosphite Chemical compound CCCCCCCCCCCCCCCCCCOP(OCCCCCCCCCCCCCCCCCC)OCCCCCCCCCCCCCCCCCC CNUJLMSKURPSHE-UHFFFAOYSA-N 0.000 description 1
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- XOOUIPVCVHRTMJ-UHFFFAOYSA-L zinc stearate Chemical compound [Zn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O XOOUIPVCVHRTMJ-UHFFFAOYSA-L 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
- C08L23/02—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
-
- 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
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/32—Phosphorus-containing compounds
-
- 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
- C08K5/34924—Triazines containing cyanurate groups; Tautomers thereof
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)
- Agricultural Chemicals And Associated Chemicals (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE4225477 | 1992-08-01 | ||
| DE4225477 | 1992-08-01 |
Publications (2)
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|---|---|
| AU4428593A AU4428593A (en) | 1994-02-03 |
| AU665442B2 true AU665442B2 (en) | 1996-01-04 |
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AU44285/93A Ceased AU665442B2 (en) | 1992-08-01 | 1993-07-30 | Flame-retardant plastics molding composition of improved stability |
Country Status (15)
| Country | Link |
|---|---|
| US (1) | US5326805A (enExample) |
| EP (1) | EP0584567B1 (enExample) |
| JP (1) | JP3351870B2 (enExample) |
| KR (1) | KR940005739A (enExample) |
| AT (1) | ATE162836T1 (enExample) |
| AU (1) | AU665442B2 (enExample) |
| CA (1) | CA2101655C (enExample) |
| DE (1) | DE59308059D1 (enExample) |
| DK (1) | DK0584567T3 (enExample) |
| ES (1) | ES2114577T3 (enExample) |
| FI (1) | FI110117B (enExample) |
| MY (1) | MY108932A (enExample) |
| NO (1) | NO301377B1 (enExample) |
| TW (1) | TW252135B (enExample) |
| ZA (1) | ZA935519B (enExample) |
Families Citing this family (88)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE19511928A1 (de) * | 1995-03-31 | 1997-01-02 | Hoechst Ag | Flammwidrige Überzugsmasse |
| DE19546834A1 (de) * | 1995-12-15 | 1997-06-19 | Hoechst Ag | Flammwidrige polymere Massen |
| DE19614424A1 (de) | 1996-04-12 | 1997-10-16 | Hoechst Ag | Synergistische Flammschutzmittel-Kombination für Polymere |
| DE19734437A1 (de) | 1997-08-08 | 1999-02-11 | Clariant Gmbh | Synergistische Flammschutzmittel-Kombination für Polymere |
| DE19737727A1 (de) | 1997-08-29 | 1999-07-08 | Clariant Gmbh | Synergistische Flammschutzmittel-Kombination für Kunststoffe |
| DE19820398A1 (de) | 1998-05-07 | 1999-11-11 | Basf Ag | Flammgeschützte Polyesterformmassen |
| DE19830128A1 (de) | 1998-07-06 | 2000-02-10 | Degussa | Oberflächenmodifizierte Flammschutzmittel, Verfahren zu deren Herstellung sowie deren Verwendung |
| WO2000012608A1 (en) * | 1998-08-31 | 2000-03-09 | General Electric Company | Flame resistant polyketone resin compositions |
| ATE313597T1 (de) | 1999-01-30 | 2006-01-15 | Clariant Gmbh | Flammschutzmittel-kombination für thermoplastische polymere i |
| DE19903709A1 (de) | 1999-01-30 | 2000-08-10 | Clariant Gmbh | Flammschutzmittel-Kombination für thermoplastische Polymere II |
| DE19903707C2 (de) | 1999-01-30 | 2003-05-28 | Clariant Gmbh | Flammwidrige duroplastische Massen |
| DE19933901A1 (de) | 1999-07-22 | 2001-02-01 | Clariant Gmbh | Flammschutzmittel-Kombination |
| DE10007672A1 (de) * | 2000-02-19 | 2001-08-23 | Mitsubishi Polyester Film Gmbh | Weiß-opake, schwer entflammbare, UV-stabilisierte Folie mit niedriger Transparenz aus einem kristallisierbaren Thermoplasten |
| GB2371559A (en) * | 2001-01-26 | 2002-07-31 | Clariant Int Ltd | Tanning process and agents |
| US7084196B2 (en) * | 2001-03-20 | 2006-08-01 | Ciba Specialty Chemicals Corporation | Flame retardant compositions |
| JP2002338756A (ja) * | 2001-05-16 | 2002-11-27 | Calp Corp | 難燃性樹脂組成物及びその成形体 |
| JP3920691B2 (ja) | 2002-04-12 | 2007-05-30 | 日華化学株式会社 | 難燃加工剤、難燃加工方法、及び難燃加工物 |
| EP1386942A1 (en) * | 2002-07-25 | 2004-02-04 | Clariant GmbH | Flame retardant combination |
| DE10241375A1 (de) | 2002-09-06 | 2004-03-18 | Clariant Gmbh | Granulare Flammschutzmittelzusammensetzung |
| DE10241373A1 (de) | 2002-09-06 | 2004-03-18 | Clariant Gmbh | Oberflächenmodifizierte Phosphinsäuresalze |
| DE10241376A1 (de) * | 2002-09-06 | 2004-03-18 | Clariant Gmbh | Kompaktierte Flammschutzmittelzusammensetzung |
| DE10241374B3 (de) * | 2002-09-06 | 2004-02-19 | Clariant Gmbh | Staubarme, pulverförmige Flammschutzmittelzusammensetzung, Verfahren zu deren Herstellung und deren Verwendung, sowie flammgeschützte Polymerformmassen |
| DE10244576A1 (de) * | 2002-09-25 | 2004-04-08 | Clariant Gmbh | Flammwidrige duroplastische Massen |
| DE10244578A1 (de) * | 2002-09-25 | 2004-04-08 | Clariant Gmbh | Flammwidrige duroplastische Massen |
| DE10309622A1 (de) * | 2003-03-04 | 2004-09-23 | Clariant Gmbh | Schmelzbare Zinkphosphinate |
| DE10321286B4 (de) * | 2003-05-13 | 2005-04-14 | Clariant Gmbh | Flammschutzadditiv für polymere Massen mit verbesserter hydrothermaler Stabilität |
| DE10321298B4 (de) * | 2003-05-13 | 2005-11-10 | Clariant Gmbh | Halogenhaltige Flammschutzmittel-Kombination und deren Verwendung |
| DE10324568A1 (de) | 2003-05-30 | 2005-01-13 | Clariant Gmbh | Styrol-Hypophosphit-Addukt sowie ein Verfahren zu dessen Herstellung und seine Verwendung |
| DE10331889A1 (de) * | 2003-07-14 | 2005-02-17 | Clariant Gmbh | Flammwidrige Polyamide |
| DE10346326A1 (de) * | 2003-10-06 | 2005-05-04 | Ems Chemie Ag | Flammgeschützte Polyamidformmassen und deren Verwendung |
| DE102004023085A1 (de) | 2004-05-11 | 2005-12-15 | Clariant Gmbh | Dialkylphosphinsäure-Salze, ein Verfahren zu ihrer Herstellung und ihre Verwendung |
| US7592382B2 (en) * | 2004-11-22 | 2009-09-22 | Sabic Innovative Plastics Ip B.V. | Flame retardant poly(arylene ether)/polyamide compositions, methods, and articles |
| US7534822B2 (en) * | 2004-11-22 | 2009-05-19 | Sabic Innovative Plastics Ip B.V. | Method of making a flame retardant poly(arylene ether)/polyamide composition |
| KR20070115867A (ko) * | 2004-11-22 | 2007-12-06 | 제너럴 일렉트릭 캄파니 | 난연성 폴리(아릴렌 에테르)/폴리아미드 조성물 및 그의제조 방법 |
| US7449507B2 (en) * | 2004-11-22 | 2008-11-11 | Sabic Innovative Plastics Ip B.V. | Poly(arylene ether)/polyamide composition and method of making |
| US20060111548A1 (en) * | 2004-11-22 | 2006-05-25 | Mark Elkovitch | Method of making a flame retardant poly(arylene ether)/polyamide composition and the composition thereof |
| US20060167143A1 (en) * | 2004-11-22 | 2006-07-27 | General Electric Company | Flame Retardant Poly(Arylene Ether)/Polyamide Composition |
| MX2008011341A (es) | 2006-03-16 | 2008-09-23 | Clariant Finance Bvi Ltd | Ceras modificadas, proceso para su preparacion, y su uso. |
| DE102007001862A1 (de) | 2007-01-12 | 2008-07-17 | Clariant International Ltd. | Flammwidrige Harzformulierung und ihre Verwendung |
| EP2194091A1 (en) | 2008-12-03 | 2010-06-09 | DSM IP Assets B.V. | Flame retardant thermoplastic elastomers |
| SI2493969T1 (sl) | 2009-10-27 | 2013-11-29 | Basf Se | Toplotno proti staranju odporni poliamidi z zaščito proti ognju |
| US20110237695A1 (en) * | 2010-03-23 | 2011-09-29 | Clariant International Ltd. | Flame Retardant Combinations For Polyester Elastomers And Flame Retarded Extrusion Or Molding Compositions Therefrom |
| BR112012028309A2 (pt) | 2010-05-05 | 2016-11-01 | Basf Se | "componente, e, processo para a produção de um componente" |
| DE102010023770A1 (de) | 2010-06-15 | 2011-12-15 | Basf Se | Glühdrahtbeständige Formmassen |
| DE102011087869A1 (de) | 2010-12-08 | 2012-09-06 | Basf Se | Lasermarkierbare flammgeschützte Formkörper |
| NZ590534A (en) * | 2011-01-17 | 2014-01-31 | Auckland Uniservices Ltd | Fire retardant polypropylene |
| US8987357B2 (en) | 2011-05-27 | 2015-03-24 | Basf Se | Thermoplastic molding composition |
| EP2527402A1 (de) | 2011-05-27 | 2012-11-28 | Basf Se | Thermoplastische Formmasse |
| SI2773694T1 (sl) | 2011-09-28 | 2016-07-29 | Italmatch Chemicals S.P.A. | Brezhalogenska negorljiva poliamidna sestava |
| WO2013045965A1 (en) | 2011-09-28 | 2013-04-04 | Italmatch Chemicals S.P.A. | Halogen-free flame retardant polyesters composition |
| WO2014029641A1 (de) | 2012-08-20 | 2014-02-27 | Basf Se | Langfaserverstärkte flammgeschützte polyester |
| US8962717B2 (en) | 2012-08-20 | 2015-02-24 | Basf Se | Long-fiber-reinforced flame-retardant polyesters |
| JP2016510355A (ja) | 2013-01-22 | 2016-04-07 | エフアールエックス ポリマーズ、インク． | リン含有エポキシ化合物およびそれからなる組成物 |
| CN103319748B (zh) * | 2013-06-03 | 2014-10-22 | 公安部四川消防研究所 | 磷氮复合型阻燃剂及其制备方法 |
| SG11201510168XA (en) | 2013-06-12 | 2016-01-28 | Basf Se | Process for the continuous preparation of an aliphatic or partially aromatic polyamide |
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| MX2015017204A (es) | 2013-06-12 | 2016-11-11 | Basf Se | Método para producir poliamidas alifáticas o parcialmente aromáticas, que comprende un proceso de polimerizacion de fase solida. |
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| EP2813530A1 (de) | 2013-06-12 | 2014-12-17 | Basf Se | Teilaromatische Copolyamide auf Basis von Terephthalsäure und Hexamethylendiamin |
| EP3009478B1 (en) * | 2013-06-13 | 2023-11-22 | Kuraray Co., Ltd. | Polyamide resin composition and molded article produced therefrom |
| WO2015091777A1 (de) | 2013-12-19 | 2015-06-25 | Basf Se | Verfahren zur herstellung eines aliphatischen oder teilaromatischen polyamids |
| US10808120B2 (en) | 2015-10-14 | 2020-10-20 | Basf Se | Polyester blend having a halogen-free flame protection |
| US20190031857A1 (en) | 2016-02-22 | 2019-01-31 | Basf Se | Black-colored polyamide composition and production and use thereof |
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| US11142642B2 (en) | 2017-01-30 | 2021-10-12 | Basf Se | Polyamide composition which is dyed in black, production and use thereof |
| CN107892808B (zh) * | 2017-11-22 | 2019-08-13 | 江苏利思德新材料有限公司 | 一种电线电缆用无卤阻燃tpu弹性体组合物及其制备方法 |
| CN107828204B (zh) * | 2017-11-22 | 2019-08-13 | 江苏利思德新材料有限公司 | 一种聚氨酯用无卤阻燃复配体系及其在无卤阻燃聚氨酯中的应用 |
| MX2020005347A (es) | 2017-11-23 | 2020-08-13 | Basf Se | Composicion de poliamida para la produccion de cuerpos moldeados por soldadura. |
| WO2019121506A1 (de) | 2017-12-18 | 2019-06-27 | Basf Se | Polyamid-formmassen mit verbesserten optischen eigenschaften und verwendung von farbmitteln darin |
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| WO2020016371A1 (en) | 2018-07-19 | 2020-01-23 | Basf Se | Black-colored polyamide composition, production thereof and use |
| CN112437784B (zh) | 2018-08-16 | 2024-06-28 | 巴斯夫欧洲公司 | 热塑性模塑材料 |
| KR20210132042A (ko) | 2019-02-20 | 2021-11-03 | 바스프 에스이 | 열가소성 성형 화합물 |
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| JP7500592B2 (ja) | 2019-02-25 | 2024-06-17 | ビーエーエスエフ ソシエタス・ヨーロピア | 熱可塑性成形組成物 |
| JP2023505295A (ja) | 2019-12-05 | 2023-02-08 | ビーエーエスエフ ソシエタス・ヨーロピア | 黒色に染色されたポリアミド組成物、その製造及び使用方法 |
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| WO2021170715A1 (en) | 2020-02-26 | 2021-09-02 | Basf Se | Heat-aging resistant polyamide molding compositions |
| JP2023523884A (ja) | 2020-03-20 | 2023-06-08 | ビーエーエスエフ ソシエタス・ヨーロピア | 可塑化ポリアミド成形組成物 |
| WO2021191264A1 (en) | 2020-03-25 | 2021-09-30 | Basf Se | Molded article providing an electromagnetic shielding |
| BR112022019115A2 (pt) | 2020-03-25 | 2022-11-08 | Basf Se | Composição de modelagem termoplástica, processo de preparação da composição, uso da composição e fibra, folha ou modelagem |
| DK4146727T3 (da) | 2020-05-06 | 2024-09-30 | Basf Se | Flammehæmmende polyesterblanding |
| WO2022180221A1 (en) | 2021-02-25 | 2022-09-01 | Basf Se | Polymers having improved thermal conductivity |
| JP2024522967A (ja) | 2021-04-30 | 2024-06-25 | ビーエーエスエフ ソシエタス・ヨーロピア | 脂肪族コポリアミド組成物 |
| WO2023237603A1 (en) | 2022-06-08 | 2023-12-14 | Basf Se | Recycling method for producing a polyamide compound |
| CN119948108A (zh) | 2022-09-27 | 2025-05-06 | 巴斯夫欧洲公司 | 具有改善的颜色稳定性的热塑性模塑组合物-1 |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3720094A1 (de) * | 1986-08-25 | 1988-03-03 | Hoechst Ag | Flammwidrige polymere massen |
| IT1244009B (it) * | 1990-11-02 | 1994-06-28 | Mini Ricerca Scient Tecnolog | Composizioni polimeriche autoestinguenti. |
-
1993
- 1993-07-26 TW TW082105926A patent/TW252135B/zh active
- 1993-07-28 DK DK93112058T patent/DK0584567T3/da active
- 1993-07-28 AT AT93112058T patent/ATE162836T1/de not_active IP Right Cessation
- 1993-07-28 EP EP93112058A patent/EP0584567B1/de not_active Expired - Lifetime
- 1993-07-28 ES ES93112058T patent/ES2114577T3/es not_active Expired - Lifetime
- 1993-07-28 DE DE59308059T patent/DE59308059D1/de not_active Expired - Fee Related
- 1993-07-29 FI FI933402A patent/FI110117B/fi not_active IP Right Cessation
- 1993-07-30 AU AU44285/93A patent/AU665442B2/en not_active Ceased
- 1993-07-30 MY MYPI93001501A patent/MY108932A/en unknown
- 1993-07-30 CA CA002101655A patent/CA2101655C/en not_active Expired - Fee Related
- 1993-07-30 JP JP18973293A patent/JP3351870B2/ja not_active Expired - Fee Related
- 1993-07-30 KR KR1019930014653A patent/KR940005739A/ko not_active Ceased
- 1993-07-30 ZA ZA935519A patent/ZA935519B/xx unknown
- 1993-07-30 NO NO932740A patent/NO301377B1/no unknown
- 1993-07-30 US US08/100,909 patent/US5326805A/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| ES2114577T3 (es) | 1998-06-01 |
| EP0584567B1 (de) | 1998-01-28 |
| CA2101655A1 (en) | 1994-02-02 |
| TW252135B (enExample) | 1995-07-21 |
| EP0584567A3 (en) | 1995-11-22 |
| FI933402L (fi) | 1994-02-02 |
| JP3351870B2 (ja) | 2002-12-03 |
| KR940005739A (ko) | 1994-03-22 |
| DE59308059D1 (de) | 1998-03-05 |
| FI933402A0 (fi) | 1993-07-29 |
| CA2101655C (en) | 2004-02-10 |
| EP0584567A2 (de) | 1994-03-02 |
| DK0584567T3 (da) | 1998-09-21 |
| NO301377B1 (no) | 1997-10-20 |
| ATE162836T1 (de) | 1998-02-15 |
| AU4428593A (en) | 1994-02-03 |
| NO932740L (no) | 1994-02-02 |
| MY108932A (en) | 1996-11-30 |
| JPH06172663A (ja) | 1994-06-21 |
| US5326805A (en) | 1994-07-05 |
| ZA935519B (en) | 1994-02-24 |
| FI110117B (fi) | 2002-11-29 |
| NO932740D0 (no) | 1993-07-30 |
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