ES2844323T3 - Elastómeros de copolieteramida procesables en estado fundido - Google Patents
Elastómeros de copolieteramida procesables en estado fundido Download PDFInfo
- Publication number
- ES2844323T3 ES2844323T3 ES11707743T ES11707743T ES2844323T3 ES 2844323 T3 ES2844323 T3 ES 2844323T3 ES 11707743 T ES11707743 T ES 11707743T ES 11707743 T ES11707743 T ES 11707743T ES 2844323 T3 ES2844323 T3 ES 2844323T3
- Authority
- ES
- Spain
- Prior art keywords
- lactam
- terminated
- diisocyanate
- elastomer
- copolyetheramide
- 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.)
- Active
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- 229920001971 elastomer Polymers 0.000 title claims abstract description 61
- 239000000806 elastomer Substances 0.000 title claims abstract description 61
- 125000005442 diisocyanate group Chemical group 0.000 claims abstract description 87
- DVPHDWQFZRBFND-DMHDVGBCSA-N 1-o-[2-[(3ar,5r,6s,6ar)-2,2-dimethyl-6-prop-2-enoyloxy-3a,5,6,6a-tetrahydrofuro[2,3-d][1,3]dioxol-5-yl]-2-[4-[(2s,3r)-1-butan-2-ylsulfanyl-2-(2-chlorophenyl)-4-oxoazetidin-3-yl]oxy-4-oxobutanoyl]oxyethyl] 4-o-[(2s,3r)-1-butan-2-ylsulfanyl-2-(2-chloropheny Chemical group C1([C@H]2[C@H](C(N2SC(C)CC)=O)OC(=O)CCC(=O)OC(COC(=O)CCC(=O)O[C@@H]2[C@@H](N(C2=O)SC(C)CC)C=2C(=CC=CC=2)Cl)[C@@H]2[C@@H]([C@H]3OC(C)(C)O[C@H]3O2)OC(=O)C=C)=CC=CC=C1Cl DVPHDWQFZRBFND-DMHDVGBCSA-N 0.000 claims abstract description 53
- 239000003054 catalyst Substances 0.000 claims abstract description 47
- 150000003951 lactams Chemical class 0.000 claims abstract description 47
- 238000000034 method Methods 0.000 claims abstract description 28
- 150000001875 compounds Chemical class 0.000 claims abstract description 27
- 238000006116 polymerization reaction Methods 0.000 claims abstract description 23
- 229920000909 polytetrahydrofuran Polymers 0.000 claims abstract description 23
- 238000002156 mixing Methods 0.000 claims abstract description 16
- 238000002360 preparation method Methods 0.000 claims abstract description 14
- 239000004952 Polyamide Substances 0.000 claims abstract description 7
- 239000000155 melt Substances 0.000 claims abstract description 7
- 229910052751 metal Inorganic materials 0.000 claims abstract description 7
- 239000002184 metal Substances 0.000 claims abstract description 7
- 229920002647 polyamide Polymers 0.000 claims abstract description 7
- 230000000379 polymerizing effect Effects 0.000 claims abstract description 7
- 239000007795 chemical reaction product Substances 0.000 claims abstract description 5
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract description 5
- JBKVHLHDHHXQEQ-UHFFFAOYSA-N epsilon-caprolactam Chemical compound O=C1CCCCCN1 JBKVHLHDHHXQEQ-UHFFFAOYSA-N 0.000 claims description 73
- 239000000203 mixture Substances 0.000 claims description 42
- 239000000463 material Substances 0.000 claims description 39
- 239000004970 Chain extender Substances 0.000 claims description 24
- 239000000654 additive Substances 0.000 claims description 18
- 239000005057 Hexamethylene diisocyanate Substances 0.000 claims description 12
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 claims description 12
- JHWNWJKBPDFINM-UHFFFAOYSA-N Laurolactam Chemical compound O=C1CCCCCCCCCCCN1 JHWNWJKBPDFINM-UHFFFAOYSA-N 0.000 claims description 8
- -1 antiozonates Substances 0.000 claims description 6
- 239000004305 biphenyl Substances 0.000 claims description 6
- 235000010290 biphenyl Nutrition 0.000 claims description 5
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 claims description 5
- 239000000049 pigment Substances 0.000 claims description 5
- 239000003963 antioxidant agent Substances 0.000 claims description 4
- 125000006267 biphenyl group Chemical group 0.000 claims description 4
- DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 claims description 4
- KXBFLNPZHXDQLV-UHFFFAOYSA-N [cyclohexyl(diisocyanato)methyl]cyclohexane Chemical compound C1CCCCC1C(N=C=O)(N=C=O)C1CCCCC1 KXBFLNPZHXDQLV-UHFFFAOYSA-N 0.000 claims description 3
- 239000000945 filler Substances 0.000 claims description 3
- 239000004611 light stabiliser Substances 0.000 claims description 3
- 239000000314 lubricant Substances 0.000 claims description 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 3
- 239000003381 stabilizer Substances 0.000 claims description 3
- 239000004609 Impact Modifier Substances 0.000 claims description 2
- 239000006057 Non-nutritive feed additive Substances 0.000 claims description 2
- 239000012963 UV stabilizer Substances 0.000 claims description 2
- 239000003086 colorant Substances 0.000 claims description 2
- 229920001940 conductive polymer Polymers 0.000 claims description 2
- 229910052500 inorganic mineral Inorganic materials 0.000 claims description 2
- 239000011707 mineral Substances 0.000 claims description 2
- 239000002105 nanoparticle Substances 0.000 claims description 2
- 239000002071 nanotube Substances 0.000 claims description 2
- 230000003068 static effect Effects 0.000 claims description 2
- 229920005862 polyol Polymers 0.000 description 34
- 150000003077 polyols Chemical class 0.000 description 34
- 238000006243 chemical reaction Methods 0.000 description 23
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 17
- 150000002009 diols Chemical class 0.000 description 16
- 229920000570 polyether Polymers 0.000 description 16
- 239000004721 Polyphenylene oxide Substances 0.000 description 15
- 229920002614 Polyether block amide Polymers 0.000 description 14
- 238000009472 formulation Methods 0.000 description 13
- VPRUMANMDWQMNF-UHFFFAOYSA-N phenylethane boronic acid Chemical compound OB(O)CCC1=CC=CC=C1 VPRUMANMDWQMNF-UHFFFAOYSA-N 0.000 description 13
- MOMGDEWWZBKDDR-UHFFFAOYSA-M sodium;3,4,5,6-tetrahydro-2h-azepin-7-olate Chemical compound [Na+].O=C1CCCCC[N-]1 MOMGDEWWZBKDDR-UHFFFAOYSA-M 0.000 description 13
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 10
- 239000000178 monomer Substances 0.000 description 9
- 238000005191 phase separation Methods 0.000 description 8
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 7
- 150000001408 amides Chemical class 0.000 description 7
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 7
- UPMLOUAZCHDJJD-UHFFFAOYSA-N 4,4'-Diphenylmethane Diisocyanate Chemical compound C1=CC(N=C=O)=CC=C1CC1=CC=C(N=C=O)C=C1 UPMLOUAZCHDJJD-UHFFFAOYSA-N 0.000 description 6
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
- 238000004458 analytical method Methods 0.000 description 6
- 239000003153 chemical reaction reagent Substances 0.000 description 6
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 6
- 125000004356 hydroxy functional group Chemical group O* 0.000 description 6
- 125000004432 carbon atom Chemical group C* 0.000 description 5
- 238000007906 compression Methods 0.000 description 5
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- BJZYYSAMLOBSDY-QMMMGPOBSA-N (2s)-2-butoxybutan-1-ol Chemical group CCCCO[C@@H](CC)CO BJZYYSAMLOBSDY-QMMMGPOBSA-N 0.000 description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- 229920001400 block copolymer Polymers 0.000 description 4
- 125000004122 cyclic group Chemical group 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- 238000010998 test method Methods 0.000 description 4
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 150000004985 diamines Chemical class 0.000 description 3
- 230000008020 evaporation Effects 0.000 description 3
- 238000001704 evaporation Methods 0.000 description 3
- 150000002334 glycols Chemical class 0.000 description 3
- XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 description 3
- 239000000543 intermediate Substances 0.000 description 3
- HNJBEVLQSNELDL-UHFFFAOYSA-N pyrrolidin-2-one Chemical compound O=C1CCCN1 HNJBEVLQSNELDL-UHFFFAOYSA-N 0.000 description 3
- PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-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
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 2
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 2
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- XMUZQOKACOLCSS-UHFFFAOYSA-N [2-(hydroxymethyl)phenyl]methanol Chemical compound OCC1=CC=CC=C1CO XMUZQOKACOLCSS-UHFFFAOYSA-N 0.000 description 2
- 239000006096 absorbing agent Substances 0.000 description 2
- 125000002947 alkylene group Chemical group 0.000 description 2
- WULPUQZASCZTPO-UHFFFAOYSA-N azacycloundecan-2-one Chemical compound O=C1CCCCCCCCCN1 WULPUQZASCZTPO-UHFFFAOYSA-N 0.000 description 2
- KBLFLMTZLPQGIF-UHFFFAOYSA-N azecan-2-one Chemical compound O=C1CCCCCCCCN1 KBLFLMTZLPQGIF-UHFFFAOYSA-N 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
- 239000006227 byproduct Substances 0.000 description 2
- YCIMNLLNPGFGHC-UHFFFAOYSA-N catechol Chemical compound OC1=CC=CC=C1O YCIMNLLNPGFGHC-UHFFFAOYSA-N 0.000 description 2
- UHZZMRAGKVHANO-UHFFFAOYSA-M chlormequat chloride Chemical compound [Cl-].C[N+](C)(C)CCCl UHZZMRAGKVHANO-UHFFFAOYSA-M 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 238000011437 continuous method Methods 0.000 description 2
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- DIOQZVSQGTUSAI-UHFFFAOYSA-N decane Chemical compound CCCCCCCCCC DIOQZVSQGTUSAI-UHFFFAOYSA-N 0.000 description 2
- 238000000113 differential scanning calorimetry Methods 0.000 description 2
- 238000001125 extrusion Methods 0.000 description 2
- 239000013020 final formulation Substances 0.000 description 2
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- 239000011777 magnesium Substances 0.000 description 2
- 229910052749 magnesium Inorganic materials 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- XUWHAWMETYGRKB-UHFFFAOYSA-N piperidin-2-one Chemical compound O=C1CCCCN1 XUWHAWMETYGRKB-UHFFFAOYSA-N 0.000 description 2
- 229920001610 polycaprolactone Polymers 0.000 description 2
- 229920000515 polycarbonate Polymers 0.000 description 2
- 239000004417 polycarbonate Substances 0.000 description 2
- 229920000728 polyester Polymers 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 239000011591 potassium Substances 0.000 description 2
- 229910052700 potassium Inorganic materials 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 2
- 238000005549 size reduction Methods 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 239000008096 xylene Substances 0.000 description 2
- HJIAMFHSAAEUKR-UHFFFAOYSA-N (2-hydroxyphenyl)-phenylmethanone Chemical class OC1=CC=CC=C1C(=O)C1=CC=CC=C1 HJIAMFHSAAEUKR-UHFFFAOYSA-N 0.000 description 1
- RTTZISZSHSCFRH-UHFFFAOYSA-N 1,3-bis(isocyanatomethyl)benzene Chemical compound O=C=NCC1=CC=CC(CN=C=O)=C1 RTTZISZSHSCFRH-UHFFFAOYSA-N 0.000 description 1
- 239000005059 1,4-Cyclohexyldiisocyanate Substances 0.000 description 1
- SBJCUZQNHOLYMD-UHFFFAOYSA-N 1,5-Naphthalene diisocyanate Chemical compound C1=CC=C2C(N=C=O)=CC=CC2=C1N=C=O SBJCUZQNHOLYMD-UHFFFAOYSA-N 0.000 description 1
- VZSRBBMJRBPUNF-UHFFFAOYSA-N 2-(2,3-dihydro-1H-inden-2-ylamino)-N-[3-oxo-3-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)propyl]pyrimidine-5-carboxamide Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)C(=O)NCCC(N1CC2=C(CC1)NN=N2)=O VZSRBBMJRBPUNF-UHFFFAOYSA-N 0.000 description 1
- JWTDCPGVNRBTKT-UHFFFAOYSA-N 2-[2-(2-hydroxyethoxy)phenoxy]ethanol Chemical compound OCCOC1=CC=CC=C1OCCO JWTDCPGVNRBTKT-UHFFFAOYSA-N 0.000 description 1
- QCYAJCGCGWQKJT-UHFFFAOYSA-N 2-[3-(2-hydroxyethyl)phenyl]ethanol Chemical compound OCCC1=CC=CC(CCO)=C1 QCYAJCGCGWQKJT-UHFFFAOYSA-N 0.000 description 1
- WTPYFJNYAMXZJG-UHFFFAOYSA-N 2-[4-(2-hydroxyethoxy)phenoxy]ethanol Chemical compound OCCOC1=CC=C(OCCO)C=C1 WTPYFJNYAMXZJG-UHFFFAOYSA-N 0.000 description 1
- YOVRNJUIHVNXCB-UHFFFAOYSA-N 2-oxo-n-[6-[(2-oxoazepane-1-carbonyl)amino]hexyl]azepane-1-carboxamide Chemical compound C1CCCCC(=O)N1C(=O)NCCCCCCNC(=O)N1CCCCCC1=O YOVRNJUIHVNXCB-UHFFFAOYSA-N 0.000 description 1
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- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
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- 150000007944 thiolates Chemical class 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 239000010456 wollastonite Substances 0.000 description 1
- 229910052882 wollastonite Inorganic materials 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G69/00—Macromolecular compounds obtained by reactions forming a carboxylic amide link in the main chain of the macromolecule
- C08G69/40—Polyamides containing oxygen in the form of ether groups
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/40—High-molecular-weight compounds
- C08G18/48—Polyethers
- C08G18/4854—Polyethers containing oxyalkylene groups having four carbon atoms in the alkylene group
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
- C08G18/72—Polyisocyanates or polyisothiocyanates
- C08G18/80—Masked polyisocyanates
- C08G18/8061—Masked polyisocyanates masked with compounds having only one group containing active hydrogen
- C08G18/807—Masked polyisocyanates masked with compounds having only one group containing active hydrogen with nitrogen containing compounds
- C08G18/8074—Lactams
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G69/00—Macromolecular compounds obtained by reactions forming a carboxylic amide link in the main chain of the macromolecule
- C08G69/02—Polyamides derived from amino-carboxylic acids or from polyamines and polycarboxylic acids
- C08G69/08—Polyamides derived from amino-carboxylic acids or from polyamines and polycarboxylic acids derived from amino-carboxylic acids
- C08G69/14—Lactams
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G69/00—Macromolecular compounds obtained by reactions forming a carboxylic amide link in the main chain of the macromolecule
- C08G69/02—Polyamides derived from amino-carboxylic acids or from polyamines and polycarboxylic acids
- C08G69/08—Polyamides derived from amino-carboxylic acids or from polyamines and polycarboxylic acids derived from amino-carboxylic acids
- C08G69/14—Lactams
- C08G69/16—Preparatory processes
- C08G69/18—Anionic polymerisation
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G69/00—Macromolecular compounds obtained by reactions forming a carboxylic amide link in the main chain of the macromolecule
- C08G69/02—Polyamides derived from amino-carboxylic acids or from polyamines and polycarboxylic acids
- C08G69/08—Polyamides derived from amino-carboxylic acids or from polyamines and polycarboxylic acids derived from amino-carboxylic acids
- C08G69/14—Lactams
- C08G69/16—Preparatory processes
- C08G69/18—Anionic polymerisation
- C08G69/20—Anionic polymerisation characterised by the catalysts used
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L77/00—Compositions of polyamides obtained by reactions forming a carboxylic amide link in the main chain; Compositions of derivatives of such polymers
- C08L77/02—Polyamides derived from omega-amino carboxylic acids or from lactams thereof
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Polyamides (AREA)
- Polyurethanes Or Polyureas (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US30907610P | 2010-03-01 | 2010-03-01 | |
| PCT/US2011/026018 WO2011109211A1 (en) | 2010-03-01 | 2011-02-24 | Melt processable copolyetheramide elastomers |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES2844323T3 true ES2844323T3 (es) | 2021-07-21 |
Family
ID=43972726
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES11707743T Active ES2844323T3 (es) | 2010-03-01 | 2011-02-24 | Elastómeros de copolieteramida procesables en estado fundido |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US8722794B2 (enExample) |
| EP (1) | EP2542603B1 (enExample) |
| JP (2) | JP6084465B2 (enExample) |
| CN (1) | CN102781991B (enExample) |
| CA (1) | CA2790565C (enExample) |
| ES (1) | ES2844323T3 (enExample) |
| HU (1) | HUE053245T2 (enExample) |
| TW (1) | TWI500694B (enExample) |
| WO (1) | WO2011109211A1 (enExample) |
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US9139752B2 (en) * | 2011-09-28 | 2015-09-22 | Basf Se | Process for producing polyamides via anionic polymerization |
| CN104497570A (zh) * | 2014-12-17 | 2015-04-08 | 江门市优巨新材料有限公司 | 一种耐高温无卤阻燃尼龙复合材料及其制备方法 |
| CN108699239B (zh) * | 2016-03-08 | 2021-09-21 | 英威达纺织（英国）有限公司 | 聚酰胺共聚物和其制备方法 |
| CN107936255B (zh) * | 2017-11-01 | 2021-03-02 | 中纺院（天津）科技发展有限公司 | 一种连续生产聚醚酰胺的方法 |
| CN112210076B (zh) * | 2019-07-11 | 2023-08-15 | 中国石油化工股份有限公司 | 一种连续化生产聚醚酰胺弹性体的方法及装置 |
| CN114174376B (zh) | 2019-07-31 | 2024-07-09 | 巴斯夫欧洲公司 | 新型嵌段共聚物 |
| CN112724660B (zh) * | 2020-12-28 | 2023-06-13 | 晋江市创达鞋业有限公司 | 轻量抗疲劳peba鞋底及其成型工艺 |
| CN114196193B (zh) * | 2021-11-19 | 2024-02-23 | 美瑞新材料股份有限公司 | 一种基于阴离子聚合制备尼龙弹性体的连续生产方法 |
| CN116120563B (zh) * | 2023-01-03 | 2024-06-25 | 万华化学集团股份有限公司 | 一种基于动态双硫键的热适应性聚醚酰胺弹性体材料及其制备方法 |
Family Cites Families (19)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3993709A (en) * | 1974-06-24 | 1976-11-23 | Monsanto Company | Polyester initiated anionic catalyzed polymerization of lactam |
| JPS59157121A (ja) * | 1983-02-25 | 1984-09-06 | Kanebo Ltd | 強化ポリアミドシ−トの製造法 |
| EP0135233B1 (en) * | 1983-08-20 | 1988-02-17 | Stamicarbon B.V. | Process for the preparation of an n-substituted carbamoyllactam compound |
| NL8302928A (nl) * | 1983-08-20 | 1985-03-18 | Stamicarbon | N-gesubstitueerde carbamoyl-lactam verbinding. |
| NL8302929A (nl) * | 1983-08-20 | 1985-03-18 | Stamicarbon | Werkwijze voor het bereiden van een n-gesubstitueerde carbamoyl-lactam verbinding. |
| NL8400006A (nl) * | 1984-01-03 | 1985-08-01 | Stamicarbon | Werkwijze voor de condensatie van imide en alkohol. |
| NL8400411A (nl) * | 1984-02-09 | 1985-09-02 | Stamicarbon | Werkwijze voor het bereiden van een nylonblokcopolymeercompositie. |
| KR870001407B1 (ko) * | 1984-03-22 | 1987-07-30 | 스태미카본 베· 뷔 | N-치환된 카로바모일-락탐 화합물의 제조방법 |
| US4626385A (en) * | 1984-03-22 | 1986-12-02 | Kaneyoshi Ashida | N-substituted carbamoyl-lactam |
| US4614615A (en) * | 1984-03-22 | 1986-09-30 | Kaneyoshi Ashida | Process for preparing an N-substituted carbamoyl-lactam compound |
| US4673722A (en) * | 1985-12-23 | 1987-06-16 | General Motors Corporation | High impact nylon/polyurea copolymer |
| NL8702950A (nl) * | 1987-12-08 | 1989-07-03 | Stamicarbon | Werkwijze voor het bereiden van een nylonblokcopolymeer. |
| NL8801914A (nl) | 1988-07-30 | 1990-02-16 | Stamicarbon | Omzettingsprodukten van met lactam geblokkeerde diisocyanaten en daarvan afgeleide polylactamblokcopolymeren. |
| DE4203297A1 (de) * | 1992-01-31 | 1993-08-05 | Fischer Karl Ind Gmbh | Verfahren zur herstellung von polyurethan- und/oder polyurethanharnstoff-elastomer |
| JPH06116385A (ja) * | 1992-10-02 | 1994-04-26 | Toray Ind Inc | 中空成形品の製造方法 |
| BE1006638A3 (nl) * | 1993-01-27 | 1994-11-03 | Dsm Nv | Werkwijze voor het bereiden van een nylonblokcopolymeer. |
| JPH0732390A (ja) * | 1993-07-15 | 1995-02-03 | Toray Ind Inc | 中空成形品の製造方法 |
| JP3838622B2 (ja) * | 2001-04-05 | 2006-10-25 | 日本ポリペンコ株式会社 | ポリアミドエラストマー成形体及びその製造方法 |
| JP2005336354A (ja) * | 2004-05-27 | 2005-12-08 | Nippon Polypenco Ltd | ポリアミドエラストマー成形体及びその製造方法。 |
-
2011
- 2011-02-24 HU HUE11707743A patent/HUE053245T2/hu unknown
- 2011-02-24 EP EP11707743.8A patent/EP2542603B1/en active Active
- 2011-02-24 CN CN201180011676.5A patent/CN102781991B/zh active Active
- 2011-02-24 JP JP2012556110A patent/JP6084465B2/ja active Active
- 2011-02-24 US US13/034,014 patent/US8722794B2/en active Active
- 2011-02-24 CA CA2790565A patent/CA2790565C/en not_active Expired - Fee Related
- 2011-02-24 ES ES11707743T patent/ES2844323T3/es active Active
- 2011-02-24 WO PCT/US2011/026018 patent/WO2011109211A1/en not_active Ceased
- 2011-02-25 TW TW100106362A patent/TWI500694B/zh active
-
2016
- 2016-06-15 JP JP2016118660A patent/JP2016164282A/ja not_active Withdrawn
Also Published As
| Publication number | Publication date |
|---|---|
| CN102781991A (zh) | 2012-11-14 |
| CA2790565C (en) | 2018-04-03 |
| US20110213076A1 (en) | 2011-09-01 |
| JP2016164282A (ja) | 2016-09-08 |
| CA2790565A1 (en) | 2011-09-09 |
| JP2013521373A (ja) | 2013-06-10 |
| EP2542603B1 (en) | 2020-11-18 |
| CN102781991B (zh) | 2015-07-29 |
| WO2011109211A1 (en) | 2011-09-09 |
| US8722794B2 (en) | 2014-05-13 |
| TW201137034A (en) | 2011-11-01 |
| HUE053245T2 (hu) | 2021-06-28 |
| JP6084465B2 (ja) | 2017-02-22 |
| EP2542603A1 (en) | 2013-01-09 |
| TWI500694B (zh) | 2015-09-21 |
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