ES2343921T3 - Sales mixtas de acidos diorganilfosfinicos y acidos carboxilicos. - Google Patents
Sales mixtas de acidos diorganilfosfinicos y acidos carboxilicos. Download PDFInfo
- Publication number
- ES2343921T3 ES2343921T3 ES08020200T ES08020200T ES2343921T3 ES 2343921 T3 ES2343921 T3 ES 2343921T3 ES 08020200 T ES08020200 T ES 08020200T ES 08020200 T ES08020200 T ES 08020200T ES 2343921 T3 ES2343921 T3 ES 2343921T3
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- Spain
- Prior art keywords
- acid
- acids
- weight
- salts
- mixed
- Prior art date
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- 239000002253 acid Substances 0.000 title claims abstract description 126
- 150000007513 acids Chemical class 0.000 title claims description 54
- 229920000642 polymer Polymers 0.000 claims abstract description 79
- 239000003063 flame retardant Substances 0.000 claims abstract description 68
- 239000000203 mixture Substances 0.000 claims abstract description 61
- -1 carboxylic acid anion Chemical class 0.000 claims abstract description 49
- 150000001768 cations Chemical class 0.000 claims abstract description 38
- 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 abstract description 36
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 32
- 238000000465 moulding Methods 0.000 claims abstract description 28
- 239000000654 additive Substances 0.000 claims abstract description 17
- 238000002360 preparation method Methods 0.000 claims abstract description 13
- 125000003118 aryl group Chemical group 0.000 claims abstract description 9
- ACVYVLVWPXVTIT-UHFFFAOYSA-M phosphinate Chemical compound [O-][PH2]=O ACVYVLVWPXVTIT-UHFFFAOYSA-M 0.000 claims abstract description 9
- 150000001450 anions Chemical class 0.000 claims abstract description 7
- 239000000835 fiber Substances 0.000 claims abstract description 7
- 239000000463 material Substances 0.000 claims abstract description 6
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- 230000002363 herbicidal effect Effects 0.000 claims abstract description 3
- 239000004009 herbicide Substances 0.000 claims abstract description 3
- 125000002768 hydroxyalkyl group Chemical group 0.000 claims abstract description 3
- 239000000575 pesticide Substances 0.000 claims abstract description 3
- 230000008635 plant growth Effects 0.000 claims abstract description 3
- 150000003839 salts Chemical class 0.000 claims description 88
- 150000001735 carboxylic acids Chemical class 0.000 claims description 65
- 238000000034 method Methods 0.000 claims description 40
- 229910052782 aluminium Inorganic materials 0.000 claims description 26
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 24
- KKEYFWRCBNTPAC-UHFFFAOYSA-N terephthalic acid group Chemical group C(C1=CC=C(C(=O)O)C=C1)(=O)O KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 claims description 22
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims description 17
- 239000012757 flame retardant agent Substances 0.000 claims description 14
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 claims description 11
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 claims description 9
- 229910052725 zinc Inorganic materials 0.000 claims description 9
- 239000011701 zinc Substances 0.000 claims description 9
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- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Substances [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 8
- ACVYVLVWPXVTIT-UHFFFAOYSA-N phosphinic acid Chemical compound O[PH2]=O ACVYVLVWPXVTIT-UHFFFAOYSA-N 0.000 claims description 8
- 229920000728 polyester Polymers 0.000 claims description 8
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims description 7
- 150000001875 compounds Chemical class 0.000 claims description 7
- 150000001991 dicarboxylic acids Chemical class 0.000 claims description 7
- 229910052751 metal Inorganic materials 0.000 claims description 7
- 239000002184 metal Substances 0.000 claims description 7
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 claims description 6
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical compound OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 claims description 6
- 239000007983 Tris buffer Substances 0.000 claims description 6
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- 229910052749 magnesium Inorganic materials 0.000 claims description 5
- 239000011777 magnesium Substances 0.000 claims description 5
- 239000003381 stabilizer Substances 0.000 claims description 5
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 claims description 4
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims description 4
- 230000000996 additive effect Effects 0.000 claims description 4
- GDVKFRBCXAPAQJ-UHFFFAOYSA-A dialuminum;hexamagnesium;carbonate;hexadecahydroxide Chemical compound [OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Al+3].[Al+3].[O-]C([O-])=O GDVKFRBCXAPAQJ-UHFFFAOYSA-A 0.000 claims description 4
- 229910001701 hydrotalcite Inorganic materials 0.000 claims description 4
- 229960001545 hydrotalcite Drugs 0.000 claims description 4
- 125000004029 hydroxymethyl group Chemical group [H]OC([H])([H])* 0.000 claims description 4
- 239000002480 mineral oil Substances 0.000 claims description 4
- 229920002635 polyurethane Polymers 0.000 claims description 4
- 230000002787 reinforcement Effects 0.000 claims description 4
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- 239000004971 Cross linker Substances 0.000 claims description 3
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 claims description 3
- CJCLBZGHMYJUDA-UHFFFAOYSA-K aluminum;benzene-1,3-dicarboxylate;diethylphosphinate Chemical group [Al+3].CCP([O-])(=O)CC.[O-]C(=O)C1=CC=CC(C([O-])=O)=C1 CJCLBZGHMYJUDA-UHFFFAOYSA-K 0.000 claims description 3
- 239000003963 antioxidant agent Substances 0.000 claims description 3
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- BFPVXOYPQMBHDJ-UHFFFAOYSA-H dialuminum;terephthalate Chemical group [Al+3].[Al+3].[O-]C(=O)C1=CC=C(C([O-])=O)C=C1.[O-]C(=O)C1=CC=C(C([O-])=O)C=C1.[O-]C(=O)C1=CC=C(C([O-])=O)C=C1 BFPVXOYPQMBHDJ-UHFFFAOYSA-H 0.000 claims description 3
- UCQFCFPECQILOL-UHFFFAOYSA-N diethyl hydrogen phosphate Chemical compound CCOP(O)(=O)OCC UCQFCFPECQILOL-UHFFFAOYSA-N 0.000 claims description 3
- KTLIMPGQZDZPSB-UHFFFAOYSA-M diethylphosphinate Chemical compound CCP([O-])(=O)CC KTLIMPGQZDZPSB-UHFFFAOYSA-M 0.000 claims description 3
- KTLIMPGQZDZPSB-UHFFFAOYSA-N diethylphosphinic acid Chemical compound CCP(O)(=O)CC KTLIMPGQZDZPSB-UHFFFAOYSA-N 0.000 claims description 3
- 239000003822 epoxy resin Substances 0.000 claims description 3
- FYIBGDKNYYMMAG-UHFFFAOYSA-N ethane-1,2-diol;terephthalic acid Chemical compound OCCO.OC(=O)C1=CC=C(C(O)=O)C=C1 FYIBGDKNYYMMAG-UHFFFAOYSA-N 0.000 claims description 3
- NXHKQBCTZHECQF-UHFFFAOYSA-N ethyl(methyl)phosphinic acid Chemical compound CCP(C)(O)=O NXHKQBCTZHECQF-UHFFFAOYSA-N 0.000 claims description 3
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 claims description 3
- 238000005470 impregnation Methods 0.000 claims description 3
- 150000002739 metals Chemical class 0.000 claims description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 3
- 230000003711 photoprotective effect Effects 0.000 claims description 3
- 229920003023 plastic Polymers 0.000 claims description 3
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- 229920000647 polyepoxide Polymers 0.000 claims description 3
- 239000002966 varnish Substances 0.000 claims description 3
- GAWIXWVDTYZWAW-UHFFFAOYSA-N C[CH]O Chemical group C[CH]O GAWIXWVDTYZWAW-UHFFFAOYSA-N 0.000 claims description 2
- 241001465754 Metazoa Species 0.000 claims description 2
- BXZAHARWAYSGTO-UHFFFAOYSA-K [Al+3].CCP([O-])=O.CCP([O-])=O.CCP([O-])=O Chemical compound [Al+3].CCP([O-])=O.CCP([O-])=O.CCP([O-])=O BXZAHARWAYSGTO-UHFFFAOYSA-K 0.000 claims description 2
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- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 claims description 2
- WVLAZEHCUADXTN-UHFFFAOYSA-K aluminum butyl(ethyl)phosphinate Chemical compound [Al+3].CCCCP([O-])(=O)CC.CCCCP([O-])(=O)CC.CCCCP([O-])(=O)CC WVLAZEHCUADXTN-UHFFFAOYSA-K 0.000 claims description 2
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- FGYBPGJIUUUVTL-UHFFFAOYSA-N benzene-1,3-dicarboxylic acid;zinc Chemical compound [Zn].OC(=O)C1=CC=CC(C(O)=O)=C1 FGYBPGJIUUUVTL-UHFFFAOYSA-N 0.000 claims description 2
- 239000011230 binding agent Substances 0.000 claims description 2
- 239000007844 bleaching agent Substances 0.000 claims description 2
- SPWAXFLJYHRRJL-UHFFFAOYSA-N butyl(ethyl)phosphinic acid Chemical compound CCCCP(O)(=O)CC SPWAXFLJYHRRJL-UHFFFAOYSA-N 0.000 claims description 2
- 229910052791 calcium Inorganic materials 0.000 claims description 2
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- 229910001382 calcium hypophosphite Inorganic materials 0.000 claims description 2
- 229940064002 calcium hypophosphite Drugs 0.000 claims description 2
- DRYHXHUXMMIMPH-UHFFFAOYSA-L calcium;diethylphosphinate Chemical compound [Ca+2].CCP([O-])(=O)CC.CCP([O-])(=O)CC DRYHXHUXMMIMPH-UHFFFAOYSA-L 0.000 claims description 2
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- KRYKVDUDEQTXQC-UHFFFAOYSA-H dialuminum;benzene-1,3-dicarboxylate Chemical compound [Al+3].[Al+3].[O-]C(=O)C1=CC=CC(C([O-])=O)=C1.[O-]C(=O)C1=CC=CC(C([O-])=O)=C1.[O-]C(=O)C1=CC=CC(C([O-])=O)=C1 KRYKVDUDEQTXQC-UHFFFAOYSA-H 0.000 claims description 2
- OZVCIJIOEZNZFL-UHFFFAOYSA-H dialuminum;phthalate Chemical compound [Al+3].[Al+3].[O-]C(=O)C1=CC=CC=C1C([O-])=O.[O-]C(=O)C1=CC=CC=C1C([O-])=O.[O-]C(=O)C1=CC=CC=C1C([O-])=O OZVCIJIOEZNZFL-UHFFFAOYSA-H 0.000 claims description 2
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- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 2
- LYYXRDZATAMURV-UHFFFAOYSA-N ethylphosphonous acid Chemical compound CCP(O)O LYYXRDZATAMURV-UHFFFAOYSA-N 0.000 claims description 2
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- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 2
- SEQVSYFEKVIYCP-UHFFFAOYSA-L magnesium hypophosphite Chemical compound [Mg+2].[O-]P=O.[O-]P=O SEQVSYFEKVIYCP-UHFFFAOYSA-L 0.000 claims description 2
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- SLKRGHBFYYVSLH-UHFFFAOYSA-K tris(dibutylphosphoryloxy)alumane Chemical compound [Al+3].CCCCP([O-])(=O)CCCC.CCCCP([O-])(=O)CCCC.CCCCP([O-])(=O)CCCC SLKRGHBFYYVSLH-UHFFFAOYSA-K 0.000 claims description 2
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- UXDZLUCNRYCZCG-UHFFFAOYSA-L zinc;phthalate Chemical compound [Zn+2].[O-]C(=O)C1=CC=CC=C1C([O-])=O UXDZLUCNRYCZCG-UHFFFAOYSA-L 0.000 claims description 2
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- HFVKYLPSHXAMME-UHFFFAOYSA-J diethylphosphinate;titanium(4+) Chemical compound [Ti+4].CCP([O-])(=O)CC.CCP([O-])(=O)CC.CCP([O-])(=O)CC.CCP([O-])(=O)CC HFVKYLPSHXAMME-UHFFFAOYSA-J 0.000 claims 2
- 229910001377 aluminum hypophosphite Inorganic materials 0.000 claims 1
- PPYGOLMZUNREJY-UHFFFAOYSA-K aluminum;bis(hydroxymethyl)phosphinate Chemical compound [Al+3].OCP([O-])(=O)CO.OCP([O-])(=O)CO.OCP([O-])(=O)CO PPYGOLMZUNREJY-UHFFFAOYSA-K 0.000 claims 1
- UUAARYXSOYDWSN-UHFFFAOYSA-K diethylphosphinate iron(3+) Chemical compound [Fe+3].CCP([O-])(=O)CC.CCP([O-])(=O)CC.CCP([O-])(=O)CC UUAARYXSOYDWSN-UHFFFAOYSA-K 0.000 claims 1
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- UYISKGVFPMWFJV-UHFFFAOYSA-N terephthalic acid;zinc Chemical compound [Zn].OC(=O)C1=CC=C(C(O)=O)C=C1 UYISKGVFPMWFJV-UHFFFAOYSA-N 0.000 claims 1
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- 238000003860 storage Methods 0.000 description 1
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- 239000011115 styrene butadiene Substances 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- 229920000468 styrene butadiene styrene block copolymer Polymers 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 150000004763 sulfides Chemical class 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- 239000012209 synthetic fiber Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- MHSKRLJMQQNJNC-UHFFFAOYSA-N terephthalamide Chemical compound NC(=O)C1=CC=C(C(N)=O)C=C1 MHSKRLJMQQNJNC-UHFFFAOYSA-N 0.000 description 1
- KKEYFWRCBNTPAC-UHFFFAOYSA-L terephthalate(2-) Chemical compound [O-]C(=O)C1=CC=C(C([O-])=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-L 0.000 description 1
- ZTUXEFFFLOVXQE-UHFFFAOYSA-N tetradecanoic acid Chemical compound CCCCCCCCCCCCCC(O)=O.CCCCCCCCCCCCCC(O)=O ZTUXEFFFLOVXQE-UHFFFAOYSA-N 0.000 description 1
- 238000005979 thermal decomposition reaction Methods 0.000 description 1
- 238000001149 thermolysis Methods 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- 230000007704 transition Effects 0.000 description 1
- 230000017105 transposition Effects 0.000 description 1
- 150000003918 triazines Chemical class 0.000 description 1
- 229920006337 unsaturated polyester resin Polymers 0.000 description 1
- NQPDZGIKBAWPEJ-UHFFFAOYSA-N valeric acid Chemical compound CCCCC(O)=O NQPDZGIKBAWPEJ-UHFFFAOYSA-N 0.000 description 1
- 230000017260 vegetative to reproductive phase transition of meristem Effects 0.000 description 1
- 229920001866 very low density polyethylene Polymers 0.000 description 1
- 239000010457 zeolite Substances 0.000 description 1
- 239000004246 zinc acetate Substances 0.000 description 1
- UGZADUVQMDAIAO-UHFFFAOYSA-L zinc hydroxide Chemical compound [OH-].[OH-].[Zn+2] UGZADUVQMDAIAO-UHFFFAOYSA-L 0.000 description 1
- 229940007718 zinc hydroxide Drugs 0.000 description 1
- 229910021511 zinc hydroxide Inorganic materials 0.000 description 1
- MQWLIFWNJWLDCI-UHFFFAOYSA-L zinc;carbonate;hydrate Chemical compound O.[Zn+2].[O-]C([O-])=O MQWLIFWNJWLDCI-UHFFFAOYSA-L 0.000 description 1
- CPYIZQLXMGRKSW-UHFFFAOYSA-N zinc;iron(3+);oxygen(2-) Chemical compound [O-2].[O-2].[O-2].[O-2].[Fe+3].[Fe+3].[Zn+2] CPYIZQLXMGRKSW-UHFFFAOYSA-N 0.000 description 1
- DRDVZXDWVBGGMH-UHFFFAOYSA-N zinc;sulfide Chemical class [S-2].[Zn+2] DRDVZXDWVBGGMH-UHFFFAOYSA-N 0.000 description 1
- WWILPJGMZMMNKI-UHFFFAOYSA-L zinc;terephthalate Chemical compound [Zn+2].[O-]C(=O)C1=CC=C(C([O-])=O)C=C1 WWILPJGMZMMNKI-UHFFFAOYSA-L 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/28—Phosphorus compounds with one or more P—C bonds
- C07F9/30—Phosphinic acids [R2P(=O)(OH)]; Thiophosphinic acids ; [R2P(=X1)(X2H) (X1, X2 are each independently O, S or Se)]
- C07F9/301—Acyclic saturated acids which can have further substituents on alkyl
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C63/00—Compounds having carboxyl groups bound to a carbon atoms of six-membered aromatic rings
- C07C63/14—Monocyclic dicarboxylic acids
- C07C63/15—Monocyclic dicarboxylic acids all carboxyl groups bound to carbon atoms of the six-membered aromatic ring
- C07C63/26—1,4 - Benzenedicarboxylic acid
- C07C63/28—Salts thereof
-
- 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
-
- 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
- C08K5/5313—Phosphinic compounds, e.g. R2=P(:O)OR'
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L21/00—Compositions of unspecified rubbers
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Life Sciences & Earth Sciences (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- Molecular Biology (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Fireproofing Substances (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE102007057210 | 2007-11-26 | ||
| DE102007057210A DE102007057210A1 (de) | 2007-11-26 | 2007-11-26 | Mischsalze von Diorganylphosphinsäuren und Carbonsäuren |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES2343921T3 true ES2343921T3 (es) | 2010-08-12 |
Family
ID=40377605
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES08020200T Active ES2343921T3 (es) | 2007-11-26 | 2008-11-20 | Sales mixtas de acidos diorganilfosfinicos y acidos carboxilicos. |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US8221658B2 (enExample) |
| EP (1) | EP2062904B1 (enExample) |
| JP (1) | JP5448426B2 (enExample) |
| AT (1) | ATE471330T1 (enExample) |
| DE (2) | DE102007057210A1 (enExample) |
| ES (1) | ES2343921T3 (enExample) |
Families Citing this family (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20100025643A1 (en) * | 2008-07-31 | 2010-02-04 | Clariant International Ltd. | Flame-retardant mixture for thermoplastic polymers, and flame-retardant polymers |
| CN102149762B (zh) * | 2008-08-27 | 2013-07-31 | 巴斯夫欧洲公司 | 具有聚合物分散剂的阻燃组合物 |
| US8604105B2 (en) | 2010-09-03 | 2013-12-10 | Eastman Chemical Company | Flame retardant copolyester compositions |
| DE102011112080A1 (de) | 2011-09-03 | 2013-03-07 | Entex Rust & Mitschke Gmbh | Einarbeitung von Additiven und Füllstoffen in einem Planetwalzenextruder oder einem Planetwalzenextruderabschnitt |
| JP6508942B2 (ja) | 2011-12-22 | 2019-05-08 | スリーエム イノベイティブ プロパティズ カンパニー | メルトブロープロセス、低収縮性メルトブローポリマー繊維及び繊維構造体、並びにメルトブロー可能なポリマー組成物 |
| WO2015087886A1 (ja) * | 2013-12-13 | 2015-06-18 | 旭化成ケミカルズ株式会社 | ポリアミド組成物、成形品、ｌｅｄ用反射板、及び熱による反射率の低下を抑制する方法 |
| DE102015223432A1 (de) * | 2015-11-26 | 2017-06-01 | Clariant International Ltd | Polymere Flammschutzmittelmischungen |
| SE539376C2 (en) * | 2016-02-03 | 2017-08-29 | Deflamo Ab | A Polymer composition comprising a fire suppressant |
| SE539377C2 (en) * | 2016-02-24 | 2017-08-29 | Deflamo Ab | A process for manufacturing of fire suppressing crystals |
| CN113480803B (zh) * | 2021-07-13 | 2024-01-12 | 韩山师范学院 | 一种阻燃聚烯烃复合材料及其制备方法和应用 |
| JP2024514058A (ja) * | 2021-10-18 | 2024-03-28 | エルジー・ケム・リミテッド | リン系難燃剤、及びこれを含む熱可塑性樹脂組成物 |
| WO2024251716A1 (en) * | 2023-06-08 | 2024-12-12 | Loramendi, S.Coop. | Sand core and sand core making method |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3001938A (en) * | 1958-04-01 | 1961-09-26 | Exxon Research Engineering Co | Lubricants containing salts of organic-substituted phosphorus - containing acids |
| US4038249A (en) * | 1973-05-14 | 1977-07-26 | Ciba-Geigy Corporation | Metal salts of benzoyloxybenzoates and compositions stabilized therewith |
| DE19614424A1 (de) * | 1996-04-12 | 1997-10-16 | Hoechst Ag | Synergistische Flammschutzmittel-Kombination für Polymere |
| DE19652009A1 (de) * | 1996-12-13 | 1998-06-18 | Hoechst Ag | Verfahren zur Herstellung von Aluminiumsalzen von Phosphinsäuren |
| EP0919560B1 (de) * | 1997-11-28 | 2004-02-25 | Clariant GmbH | Verfahren zur Herstellung von Metallsalzen von Aryl-alkylphosphinsäuren |
| DE10359815A1 (de) * | 2003-12-19 | 2005-07-28 | Clariant Gmbh | Verfahren zur Herstellung von Dialkylphosphinsäure-Salzen |
-
2007
- 2007-11-26 DE DE102007057210A patent/DE102007057210A1/de not_active Withdrawn
-
2008
- 2008-11-20 AT AT08020200T patent/ATE471330T1/de active
- 2008-11-20 ES ES08020200T patent/ES2343921T3/es active Active
- 2008-11-20 DE DE502008000794T patent/DE502008000794D1/de active Active
- 2008-11-20 EP EP08020200A patent/EP2062904B1/de not_active Not-in-force
- 2008-11-21 US US12/313,523 patent/US8221658B2/en not_active Expired - Fee Related
- 2008-11-25 JP JP2008299205A patent/JP5448426B2/ja not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| US20090137707A1 (en) | 2009-05-28 |
| DE502008000794D1 (de) | 2010-07-29 |
| ATE471330T1 (de) | 2010-07-15 |
| JP5448426B2 (ja) | 2014-03-19 |
| EP2062904B1 (de) | 2010-06-16 |
| EP2062904A1 (de) | 2009-05-27 |
| US8221658B2 (en) | 2012-07-17 |
| JP2009149862A (ja) | 2009-07-09 |
| DE102007057210A1 (de) | 2009-05-28 |
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