SK10802000A3 - Výroba polyamidov z aminonitrilov - Google Patents

Výroba polyamidov z aminonitrilov Download PDF

Info

Publication number: SK10802000A3
Authority: SK; Slovakia
Prior art keywords: liquid; mixture; water; pressure; acid
Prior art date: 1998-02-02

Application number

SK1080-2000A

Other languages

English (en)

Slovak (sk)

Inventor

Ralf Mohrschladt

Original Assignee

Basf Aktiengesellschaft

Priority date (The priority date 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 date listed.)

1998-02-02

Filing date

1999-02-02

Publication date

2001-04-09

1999-02-02 Application filed by Basf Aktiengesellschaft filed Critical Basf Aktiengesellschaft

2001-04-09 Publication of SK10802000A3 publication Critical patent/SK10802000A3/sk

Links

239000004952 Polyamide Substances 0.000 title claims abstract description 42
229920002647 polyamide Polymers 0.000 title claims abstract description 42
125000005219 aminonitrile group Chemical group 0.000 title claims abstract description 25
238000004519 manufacturing process Methods 0.000 title claims abstract description 12
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 60
239000000178 monomer Substances 0.000 claims abstract description 23
239000000284 extract Substances 0.000 claims abstract description 21
238000000605 extraction Methods 0.000 claims abstract description 21
238000006243 chemical reaction Methods 0.000 claims abstract description 17
239000000203 mixture Substances 0.000 claims description 74
238000000034 method Methods 0.000 claims description 43
239000007790 solid phase Substances 0.000 claims description 42
239000007791 liquid phase Substances 0.000 claims description 34
239000003054 catalyst Substances 0.000 claims description 33
GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 claims description 30
239000007788 liquid Substances 0.000 claims description 30
239000012071 phase Substances 0.000 claims description 29
239000007789 gas Substances 0.000 claims description 28
239000011541 reaction mixture Substances 0.000 claims description 20
QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims description 18
229920000642 polymer Polymers 0.000 claims description 18
238000002156 mixing Methods 0.000 claims description 15
150000003839 salts Chemical class 0.000 claims description 10
239000002253 acid Substances 0.000 claims description 9
239000006286 aqueous extract Substances 0.000 claims description 9
239000012736 aqueous medium Substances 0.000 claims description 9
125000004432 carbon atom Chemical group C* 0.000 claims description 9
239000007787 solid Substances 0.000 claims description 9
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229910021529 ammonia Inorganic materials 0.000 claims description 8
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125000003118 aryl group Chemical group 0.000 claims description 7
229910044991 metal oxide Inorganic materials 0.000 claims description 7
150000004706 metal oxides Chemical class 0.000 claims description 7
KBMSFJFLSXLIDJ-UHFFFAOYSA-N 6-aminohexanenitrile Chemical compound NCCCCCC#N KBMSFJFLSXLIDJ-UHFFFAOYSA-N 0.000 claims description 6
125000001931 aliphatic group Chemical group 0.000 claims description 6
150000007513 acids Chemical class 0.000 claims description 5
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OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims description 4
150000003951 lactams Chemical class 0.000 claims description 4
150000007522 mineralic acids Chemical class 0.000 claims description 2
JBKVHLHDHHXQEQ-UHFFFAOYSA-N epsilon-caprolactam Chemical compound O=C1CCCCCN1 JBKVHLHDHHXQEQ-UHFFFAOYSA-N 0.000 description 38
-1 aminoalkyl nitrile Chemical class 0.000 description 23
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150000001412 amines Chemical class 0.000 description 13
239000000049 pigment Substances 0.000 description 11
WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 10
238000006116 polymerization reaction Methods 0.000 description 10
125000003277 amino group Chemical group 0.000 description 9
229920002292 Nylon 6 Polymers 0.000 description 8
239000012632 extractable Substances 0.000 description 8
125000000524 functional group Chemical group 0.000 description 8
125000002560 nitrile group Chemical group 0.000 description 8
239000011148 porous material Substances 0.000 description 8
229920001971 elastomer Polymers 0.000 description 7
NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 description 7
KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 6
125000002843 carboxylic acid group Chemical group 0.000 description 6
150000001991 dicarboxylic acids Chemical class 0.000 description 6
CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 6
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 5
229910010413 TiO 2 Inorganic materials 0.000 description 5
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239000001361 adipic acid Substances 0.000 description 5
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239000011734 sodium Substances 0.000 description 5
239000000126 substance Substances 0.000 description 5
239000010457 zeolite Substances 0.000 description 5
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BTGRAWJCKBQKAO-UHFFFAOYSA-N adiponitrile Chemical compound N#CCCCCC#N BTGRAWJCKBQKAO-UHFFFAOYSA-N 0.000 description 4
150000001408 amides Chemical class 0.000 description 4
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230000007062 hydrolysis Effects 0.000 description 4
238000006460 hydrolysis reaction Methods 0.000 description 4
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238000004064 recycling Methods 0.000 description 4
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QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
DFPAKSUCGFBDDF-UHFFFAOYSA-N Nicotinamide Chemical group NC(=O)C1=CC=CN=C1 DFPAKSUCGFBDDF-UHFFFAOYSA-N 0.000 description 3
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 3
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238000005520 cutting process Methods 0.000 description 3
125000004122 cyclic group Chemical group 0.000 description 3
238000004821 distillation Methods 0.000 description 3
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238000007210 heterogeneous catalysis Methods 0.000 description 3
150000003949 imides Chemical class 0.000 description 3
238000005342 ion exchange Methods 0.000 description 3
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239000001301 oxygen Substances 0.000 description 3
229910052760 oxygen Inorganic materials 0.000 description 3
150000003018 phosphorus compounds Chemical class 0.000 description 3
125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 3
238000012545 processing Methods 0.000 description 3
239000000376 reactant Substances 0.000 description 3
239000007858 starting material Substances 0.000 description 3
229920001169 thermoplastic Polymers 0.000 description 3
239000004416 thermosoftening plastic Substances 0.000 description 3
MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 description 2
PBLZLIFKVPJDCO-UHFFFAOYSA-N 12-aminododecanoic acid Chemical compound NCCCCCCCCCCCC(O)=O PBLZLIFKVPJDCO-UHFFFAOYSA-N 0.000 description 2
SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 2
NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
JJMDCOVWQOJGCB-UHFFFAOYSA-N 5-aminopentanoic acid Chemical compound [NH3+]CCCCC([O-])=O JJMDCOVWQOJGCB-UHFFFAOYSA-N 0.000 description 2
SLXKOJJOQWFEFD-UHFFFAOYSA-N 6-aminohexanoic acid Chemical compound NCCCCCC(O)=O SLXKOJJOQWFEFD-UHFFFAOYSA-N 0.000 description 2
KDCGOANMDULRCW-UHFFFAOYSA-N 7H-purine Chemical compound N1=CNC2=NC=NC2=C1 KDCGOANMDULRCW-UHFFFAOYSA-N 0.000 description 2
NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 2
NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 2
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 2
JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 2
YLQBMQCUIZJEEH-UHFFFAOYSA-N Furan Chemical compound C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 2
238000004566 IR spectroscopy Methods 0.000 description 2
SIKJAQJRHWYJAI-UHFFFAOYSA-N Indole Chemical compound C1=CC=C2NC=CC2=C1 SIKJAQJRHWYJAI-UHFFFAOYSA-N 0.000 description 2
UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
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BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 2
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SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 description 2
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
235000021355 Stearic acid Nutrition 0.000 description 2
YTPLMLYBLZKORZ-UHFFFAOYSA-N Thiophene Chemical compound C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 description 2
XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 2
HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 2
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125000000217 alkyl group Chemical group 0.000 description 2
229910000147 aluminium phosphate Inorganic materials 0.000 description 2
150000001413 amino acids Chemical class 0.000 description 2
229960002684 aminocaproic acid Drugs 0.000 description 2
QMKYBPDZANOJGF-UHFFFAOYSA-N benzene-1,3,5-tricarboxylic acid Chemical compound OC(=O)C1=CC(C(O)=O)=CC(C(O)=O)=C1 QMKYBPDZANOJGF-UHFFFAOYSA-N 0.000 description 2
230000015572 biosynthetic process Effects 0.000 description 2
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239000006229 carbon black Substances 0.000 description 2
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QDOXWKRWXJOMAK-UHFFFAOYSA-N dichromium trioxide Chemical compound O=[Cr]O[Cr]=O QDOXWKRWXJOMAK-UHFFFAOYSA-N 0.000 description 2
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MRELNEQAGSRDBK-UHFFFAOYSA-N lanthanum(3+);oxygen(2-) Chemical compound [O-2].[O-2].[O-2].[La+3].[La+3] MRELNEQAGSRDBK-UHFFFAOYSA-N 0.000 description 2
239000000314 lubricant Substances 0.000 description 2
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NUJOXMJBOLGQSY-UHFFFAOYSA-N manganese dioxide Chemical compound O=[Mn]=O NUJOXMJBOLGQSY-UHFFFAOYSA-N 0.000 description 2
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YSRFBCIGFNFMPS-UHFFFAOYSA-N naphthalene-1,3,5,7-tetracarboxylic acid Chemical compound C1=C(C(O)=O)C=C(C(O)=O)C2=CC(C(=O)O)=CC(C(O)=O)=C21 YSRFBCIGFNFMPS-UHFFFAOYSA-N 0.000 description 2
LKKPNUDVOYAOBB-UHFFFAOYSA-N naphthalocyanine Chemical compound N1C(N=C2C3=CC4=CC=CC=C4C=C3C(N=C3C4=CC5=CC=CC=C5C=C4C(=N4)N3)=N2)=C(C=C2C(C=CC=C2)=C2)C2=C1N=C1C2=CC3=CC=CC=C3C=C2C4=N1 LKKPNUDVOYAOBB-UHFFFAOYSA-N 0.000 description 2
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239000003381 stabilizer Substances 0.000 description 2
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239000007848 Bronsted acid Substances 0.000 description 1
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239000004970 Chain extender Substances 0.000 description 1
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239000004593 Epoxy Substances 0.000 description 1
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239000005977 Ethylene Substances 0.000 description 1
PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 1
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239000006057 Non-nutritive feed additive Substances 0.000 description 1
239000005642 Oleic acid Substances 0.000 description 1
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NRTJGTSOTDBPDE-UHFFFAOYSA-N [dimethyl(methylsilyloxy)silyl]oxy-dimethyl-trimethylsilyloxysilane Chemical compound C[SiH2]O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)C NRTJGTSOTDBPDE-UHFFFAOYSA-N 0.000 description 1
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238000010348 incorporation Methods 0.000 description 1
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239000003999 initiator Substances 0.000 description 1
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150000004694 iodide salts Chemical class 0.000 description 1
229910052742 iron Inorganic materials 0.000 description 1
ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Chemical compound OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 description 1
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150000002576 ketones Chemical class 0.000 description 1
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150000004668 long chain fatty acids Chemical class 0.000 description 1
230000002934 lysing effect Effects 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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239000002184 metal Substances 0.000 description 1
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229910052901 montmorillonite Inorganic materials 0.000 description 1
ZETYUTMSJWMKNQ-UHFFFAOYSA-N n,n',n'-trimethylhexane-1,6-diamine Chemical compound CNCCCCCCN(C)C ZETYUTMSJWMKNQ-UHFFFAOYSA-N 0.000 description 1
GOQYKNQRPGWPLP-UHFFFAOYSA-N n-heptadecyl alcohol Natural products CCCCCCCCCCCCCCCCCO GOQYKNQRPGWPLP-UHFFFAOYSA-N 0.000 description 1
KYTZHLUVELPASH-UHFFFAOYSA-N naphthalene-1,2-dicarboxylic acid Chemical compound C1=CC=CC2=C(C(O)=O)C(C(=O)O)=CC=C21 KYTZHLUVELPASH-UHFFFAOYSA-N 0.000 description 1
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150000002894 organic compounds Chemical class 0.000 description 1
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239000002245 particle Substances 0.000 description 1
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230000000737 periodic effect Effects 0.000 description 1
230000005501 phase interface Effects 0.000 description 1
150000002989 phenols Chemical class 0.000 description 1
229910052698 phosphorus Inorganic materials 0.000 description 1
239000011574 phosphorus Substances 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
IEQIEDJGQAUEQZ-UHFFFAOYSA-N phthalocyanine Chemical compound N1C(N=C2C3=CC=CC=C3C(N=C3C4=CC=CC=C4C(=N4)N3)=N2)=C(C=CC=C2)C2=C1N=C1C2=CC=CC=C2C4=N1 IEQIEDJGQAUEQZ-UHFFFAOYSA-N 0.000 description 1
239000004014 plasticizer Substances 0.000 description 1
229920001484 poly(alkylene) Polymers 0.000 description 1
229920000412 polyarylene Polymers 0.000 description 1
229920000728 polyester Polymers 0.000 description 1
229920002959 polymer blend Polymers 0.000 description 1
150000004032 porphyrins Chemical class 0.000 description 1
229910052700 potassium Inorganic materials 0.000 description 1
239000011591 potassium Substances 0.000 description 1
239000000843 powder Substances 0.000 description 1
235000019260 propionic acid Nutrition 0.000 description 1
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
CHGYKYXGIWNSCD-UHFFFAOYSA-N pyridine-2,4,6-tricarboxylic acid Chemical compound OC(=O)C1=CC(C(O)=O)=NC(C(O)=O)=C1 CHGYKYXGIWNSCD-UHFFFAOYSA-N 0.000 description 1
CYIDZMCFTVVTJO-UHFFFAOYSA-N pyromellitic acid Chemical compound OC(=O)C1=CC(C(O)=O)=C(C(O)=O)C=C1C(O)=O CYIDZMCFTVVTJO-UHFFFAOYSA-N 0.000 description 1
IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
238000011084 recovery Methods 0.000 description 1
238000010992 reflux Methods 0.000 description 1
238000007142 ring opening reaction Methods 0.000 description 1
150000003902 salicylic acid esters Chemical class 0.000 description 1
150000003336 secondary aromatic amines Chemical class 0.000 description 1
150000004756 silanes Chemical class 0.000 description 1
RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
239000000377 silicon dioxide Substances 0.000 description 1
238000000638 solvent extraction Methods 0.000 description 1
229910052596 spinel Inorganic materials 0.000 description 1
239000011029 spinel Substances 0.000 description 1
150000003460 sulfonic acids Chemical class 0.000 description 1
ISIJQEHRDSCQIU-UHFFFAOYSA-N tert-butyl 2,7-diazaspiro[4.5]decane-7-carboxylate Chemical compound C1N(C(=O)OC(C)(C)C)CCCC11CNCC1 ISIJQEHRDSCQIU-UHFFFAOYSA-N 0.000 description 1
125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
239000012815 thermoplastic material Substances 0.000 description 1
229920006346 thermoplastic polyester elastomer Polymers 0.000 description 1
229930192474 thiophene Natural products 0.000 description 1
ZNOCGWVLWPVKAO-UHFFFAOYSA-N trimethoxy(phenyl)silane Chemical compound CO[Si](OC)(OC)C1=CC=CC=C1 ZNOCGWVLWPVKAO-UHFFFAOYSA-N 0.000 description 1
WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 description 1
229910052721 tungsten Inorganic materials 0.000 description 1
239000010937 tungsten Substances 0.000 description 1
ISIQQQYKUPBYSL-UHFFFAOYSA-N undecanedinitrile Chemical compound N#CCCCCCCCCCC#N ISIQQQYKUPBYSL-UHFFFAOYSA-N 0.000 description 1
238000003809 water extraction Methods 0.000 description 1
239000012463 white pigment Substances 0.000 description 1
239000011592 zinc chloride Substances 0.000 description 1
235000005074 zinc chloride Nutrition 0.000 description 1
239000011787 zinc oxide Substances 0.000 description 1
229910001928 zirconium oxide Inorganic materials 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
- 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
- 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
- C08G69/04—Preparatory processes
- 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
- 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

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Chemical & Material Sciences (AREA)
Health & Medical Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Organic Chemistry (AREA)
Polyamides (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

SK1080-2000A 1998-02-02 1999-02-02 Výroba polyamidov z aminonitrilov SK10802000A3 (sk)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
DE19804020A DE19804020A1 (de)	1998-02-02	1998-02-02	Verfahren zur Herstellung von Polyamiden aus Aminonitrilen
PCT/EP1999/000653 WO1999038907A1 (de)	1998-02-02	1999-02-02	Verfahren zur herstellung von polyamiden aus aminonitrilen

Publications (1)

Publication Number	Publication Date
SK10802000A3 true SK10802000A3 (sk)	2001-04-09

Family

ID=7856395

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
SK1080-2000A SK10802000A3 (sk)	1998-02-02	1999-02-02	Výroba polyamidov z aminonitrilov

Country Status (20)

Country	Link
US (1)	US6359020B1 (pt)
EP (1)	EP1053274B1 (pt)
JP (1)	JP2002501959A (pt)
KR (1)	KR100552368B1 (pt)
CN (1)	CN1165567C (pt)
AR (1)	AR018737A1 (pt)
AU (1)	AU2721899A (pt)
BG (1)	BG64709B1 (pt)
BR (1)	BR9908786B1 (pt)
CA (1)	CA2319758A1 (pt)
DE (2)	DE19804020A1 (pt)
ES (1)	ES2207932T3 (pt)
HU (1)	HU224290B1 (pt)
ID (1)	ID25866A (pt)
IL (1)	IL137165A (pt)
PL (1)	PL342239A1 (pt)
SK (1)	SK10802000A3 (pt)
TR (1)	TR200002252T2 (pt)
TW (1)	TW565580B (pt)
WO (1)	WO1999038907A1 (pt)

Families Citing this family (12)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
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1998
- 1998-02-02 DE DE19804020A patent/DE19804020A1/de not_active Withdrawn
1999
- 1999-01-28 TW TW088101311A patent/TW565580B/zh not_active IP Right Cessation
- 1999-02-01 AR ARP990100404A patent/AR018737A1/es active IP Right Grant
- 1999-02-02 EP EP99907474A patent/EP1053274B1/de not_active Expired - Lifetime
- 1999-02-02 CN CNB998026069A patent/CN1165567C/zh not_active Expired - Fee Related
- 1999-02-02 CA CA002319758A patent/CA2319758A1/en not_active Abandoned
- 1999-02-02 PL PL99342239A patent/PL342239A1/xx unknown
- 1999-02-02 AU AU27218/99A patent/AU2721899A/en not_active Abandoned
- 1999-02-02 WO PCT/EP1999/000653 patent/WO1999038907A1/de not_active Application Discontinuation
- 1999-02-02 ID IDW20001475A patent/ID25866A/id unknown
- 1999-02-02 DE DE59906953T patent/DE59906953D1/de not_active Expired - Lifetime
- 1999-02-02 US US09/600,070 patent/US6359020B1/en not_active Expired - Lifetime
- 1999-02-02 HU HU0101072A patent/HU224290B1/hu not_active IP Right Cessation
- 1999-02-02 SK SK1080-2000A patent/SK10802000A3/sk unknown
- 1999-02-02 KR KR1020007008377A patent/KR100552368B1/ko not_active IP Right Cessation
- 1999-02-02 TR TR2000/02252T patent/TR200002252T2/xx unknown
- 1999-02-02 JP JP2000529372A patent/JP2002501959A/ja not_active Withdrawn
- 1999-02-02 ES ES99907474T patent/ES2207932T3/es not_active Expired - Lifetime
- 1999-02-02 IL IL13716599A patent/IL137165A/xx not_active IP Right Cessation
- 1999-02-02 BR BRPI9908786-3A patent/BR9908786B1/pt not_active IP Right Cessation
2000
- 2000-07-13 BG BG104608A patent/BG64709B1/bg unknown

Also Published As

Publication number	Publication date
ES2207932T3 (es)	2004-06-01
US6359020B1 (en)	2002-03-19
EP1053274B1 (de)	2003-09-10
CN1165567C (zh)	2004-09-08
DE59906953D1 (de)	2003-10-16
BG64709B1 (bg)	2005-12-30
KR100552368B1 (ko)	2006-02-20
HUP0101072A3 (en)	2002-06-28
JP2002501959A (ja)	2002-01-22
TR200002252T2 (tr)	2000-12-21
AR018737A1 (es)	2001-12-12
ID25866A (id)	2000-11-09
PL342239A1 (en)	2001-06-04
BR9908786B1 (pt)	2008-11-18
CA2319758A1 (en)	1999-08-05
HU224290B1 (hu)	2005-07-28
DE19804020A1 (de)	1999-08-05
BR9908786A (pt)	2000-12-05
CN1289349A (zh)	2001-03-28
IL137165A (en)	2005-08-31
WO1999038907A1 (de)	1999-08-05
BG104608A (en)	2001-05-31
KR20010040514A (ko)	2001-05-15
IL137165A0 (en)	2001-07-24
AU2721899A (en)	1999-08-16
TW565580B (en)	2003-12-11
EP1053274A1 (de)	2000-11-22
HUP0101072A2 (hu)	2001-07-30

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