JPH0478652B2 - - Google Patents

Info

Publication number: JPH0478652B2
Authority: JP; Japan
Prior art keywords: mixture; weight; antimony oxide; carbon atoms; sodium
Prior art date: 1986-11-26
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.): Expired - Lifetime

Application number

JP27196587A

Other languages

English (en)

Japanese (ja)

Other versions

JPS63137952A (ja

Inventor

Emetsuto Garison Junia Uiriamu

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

EIDP Inc

Original Assignee

EI Du Pont de Nemours and Co

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.)

1986-11-26

Filing date

1987-10-29

Publication date

1992-12-11

1987-10-29 Application filed by EI Du Pont de Nemours and Co filed Critical EI Du Pont de Nemours and Co

1988-06-09 Publication of JPS63137952A publication Critical patent/JPS63137952A/ja

1992-12-11 Publication of JPH0478652B2 publication Critical patent/JPH0478652B2/ja

Status Granted legal-status Critical Current

Links

239000000203 mixture Substances 0.000 claims description 59
-1 polyethylene terephthalate Polymers 0.000 claims description 57
229910000410 antimony oxide Inorganic materials 0.000 claims description 32
VTRUBDSFZJNXHI-UHFFFAOYSA-N oxoantimony Chemical compound [Sb]=O VTRUBDSFZJNXHI-UHFFFAOYSA-N 0.000 claims description 32
229920000139 polyethylene terephthalate Polymers 0.000 claims description 29
239000005020 polyethylene terephthalate Substances 0.000 claims description 29
239000004952 Polyamide Substances 0.000 claims description 17
229920002647 polyamide Polymers 0.000 claims description 17
239000003063 flame retardant Substances 0.000 claims description 14
229920001577 copolymer Polymers 0.000 claims description 13
125000004432 carbon atom Chemical group C* 0.000 claims description 12
239000012141 concentrate Substances 0.000 claims description 12
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 claims description 10
229910052708 sodium Inorganic materials 0.000 claims description 10
239000011734 sodium Substances 0.000 claims description 10
239000004215 Carbon black (E152) Substances 0.000 claims description 9
229930195733 hydrocarbon Natural products 0.000 claims description 9
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 class 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 description 8
125000003118 aryl group Chemical group 0.000 claims description 8
239000004793 Polystyrene Substances 0.000 claims description 7
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 7
229920002223 polystyrene Polymers 0.000 claims description 7
239000000463 material Substances 0.000 claims description 6
238000000465 moulding Methods 0.000 claims description 6
229920000642 polymer Polymers 0.000 claims description 6
229910052736 halogen Inorganic materials 0.000 claims description 5
239000008188 pellet Substances 0.000 claims description 5
150000003628 tricarboxylic acids Chemical class 0.000 claims description 5
239000000945 filler Substances 0.000 claims description 4
150000002367 halogens Chemical class 0.000 claims description 4
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 3
150000002430 hydrocarbons Chemical class 0.000 claims description 3
239000004014 plasticizer Substances 0.000 claims description 3
CIPFDHFTBYJKQB-UHFFFAOYSA-N 1,2,3,4,5-pentachloro-6-(2,3,4,5,6-pentachlorophenoxy)benzene Chemical compound ClC1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1OC1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl CIPFDHFTBYJKQB-UHFFFAOYSA-N 0.000 claims description 2
ORYGKUIDIMIRNN-UHFFFAOYSA-N 1,2,3,4-tetrabromo-5-(2,3,4,5-tetrabromophenoxy)benzene Chemical compound BrC1=C(Br)C(Br)=CC(OC=2C(=C(Br)C(Br)=C(Br)C=2)Br)=C1Br ORYGKUIDIMIRNN-UHFFFAOYSA-N 0.000 claims description 2
IXZVOZCULZBCDY-UHFFFAOYSA-N 1,2,3,4-tetrachloro-5-(2,3,4,5-tetrachlorophenoxy)benzene Chemical compound ClC1=C(Cl)C(Cl)=CC(OC=2C(=C(Cl)C(Cl)=C(Cl)C=2)Cl)=C1Cl IXZVOZCULZBCDY-UHFFFAOYSA-N 0.000 claims description 2
DYIZJUDNMOIZQO-UHFFFAOYSA-N 4,5,6,7-tetrabromo-2-[2-(4,5,6,7-tetrabromo-1,3-dioxoisoindol-2-yl)ethyl]isoindole-1,3-dione Chemical compound O=C1C(C(=C(Br)C(Br)=C2Br)Br)=C2C(=O)N1CCN1C(=O)C2=C(Br)C(Br)=C(Br)C(Br)=C2C1=O DYIZJUDNMOIZQO-UHFFFAOYSA-N 0.000 claims description 2
229910052799 carbon Inorganic materials 0.000 claims description 2
WHHGLZMJPXIBIX-UHFFFAOYSA-N decabromodiphenyl ether Chemical compound BrC1=C(Br)C(Br)=C(Br)C(Br)=C1OC1=C(Br)C(Br)=C(Br)C(Br)=C1Br WHHGLZMJPXIBIX-UHFFFAOYSA-N 0.000 claims description 2
KNEOLQHWXNLTOV-UHFFFAOYSA-N ethene 4,5,6,7-tetrachloroisoindole-1,3-dione Chemical compound ClC=1C(=C(C(=C2C1C(=O)NC2=O)Cl)Cl)Cl.ClC=2C(=C(C(=C1C2C(=O)NC1=O)Cl)Cl)Cl.C=C KNEOLQHWXNLTOV-UHFFFAOYSA-N 0.000 claims description 2
150000002894 organic compounds Chemical class 0.000 claims description 2
159000000000 sodium salts Chemical class 0.000 claims description 2
239000004711 α-olefin Substances 0.000 claims description 2
XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 claims 2
150000001732 carboxylic acid derivatives Chemical class 0.000 claims 1
125000005843 halogen group Chemical group 0.000 claims 1
230000003014 reinforcing effect Effects 0.000 claims 1
239000002253 acid Substances 0.000 description 14
229910052783 alkali metal Inorganic materials 0.000 description 12
230000000052 comparative effect Effects 0.000 description 10
239000004677 Nylon Substances 0.000 description 8
229920002292 Nylon 6 Polymers 0.000 description 8
239000004698 Polyethylene Substances 0.000 description 8
150000007513 acids Chemical class 0.000 description 8
ADCOVFLJGNWWNZ-UHFFFAOYSA-N antimony trioxide Chemical compound O=[Sb]O[Sb]=O ADCOVFLJGNWWNZ-UHFFFAOYSA-N 0.000 description 8
238000002474 experimental method Methods 0.000 description 8
229920001778 nylon Polymers 0.000 description 8
229920000573 polyethylene Polymers 0.000 description 8
150000003839 salts Chemical class 0.000 description 7
239000000126 substance Substances 0.000 description 7
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 6
239000000654 additive Substances 0.000 description 6
WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 6
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical compound BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 6
NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 description 6
150000001340 alkali metals Chemical class 0.000 description 5
229910052794 bromium Inorganic materials 0.000 description 5
230000015556 catabolic process Effects 0.000 description 5
229910052801 chlorine Inorganic materials 0.000 description 5
150000001875 compounds Chemical class 0.000 description 5
238000006731 degradation reaction Methods 0.000 description 5
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 4
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 4
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 4
239000005977 Ethylene Substances 0.000 description 4
DTQVDTLACAAQTR-UHFFFAOYSA-N Trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-N 0.000 description 4
150000007942 carboxylates Chemical class 0.000 description 4
239000000460 chlorine Substances 0.000 description 4
239000000539 dimer Substances 0.000 description 4
238000004519 manufacturing process Methods 0.000 description 4
239000000155 melt Substances 0.000 description 4
229920005989 resin Polymers 0.000 description 4
239000011347 resin Substances 0.000 description 4
229920002302 Nylon 6,6 Polymers 0.000 description 3
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
239000001361 adipic acid Substances 0.000 description 3
235000011037 adipic acid Nutrition 0.000 description 3
125000001931 aliphatic group Chemical group 0.000 description 3
150000001412 amines Chemical group 0.000 description 3
150000001735 carboxylic acids Chemical class 0.000 description 3
239000000969 carrier Substances 0.000 description 3
238000002425 crystallisation Methods 0.000 description 3
230000008025 crystallization Effects 0.000 description 3
150000004985 diamines Chemical class 0.000 description 3
MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
JBKVHLHDHHXQEQ-UHFFFAOYSA-N epsilon-caprolactam Chemical compound O=C1CCCCCN1 JBKVHLHDHHXQEQ-UHFFFAOYSA-N 0.000 description 3
239000003365 glass fiber Substances 0.000 description 3
238000000034 method Methods 0.000 description 3
230000002787 reinforcement Effects 0.000 description 3
229920006395 saturated elastomer Polymers 0.000 description 3
WCUBBMIUIPEPOH-UHFFFAOYSA-N 4-methyl-n-octadecylbenzenesulfonamide Chemical compound CCCCCCCCCCCCCCCCCCNS(=O)(=O)C1=CC=C(C)C=C1 WCUBBMIUIPEPOH-UHFFFAOYSA-N 0.000 description 2
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 2
CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 2
229920000299 Nylon 12 Polymers 0.000 description 2
229920000305 Nylon 6,10 Polymers 0.000 description 2
229920003182 Surlyn® Polymers 0.000 description 2
XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
229910052787 antimony Inorganic materials 0.000 description 2
IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 2
238000013329 compounding Methods 0.000 description 2
238000009833 condensation Methods 0.000 description 2
230000003247 decreasing effect Effects 0.000 description 2
235000014113 dietary fatty acids Nutrition 0.000 description 2
150000002148 esters Chemical class 0.000 description 2
229920006242 ethylene acrylic acid copolymer Polymers 0.000 description 2
239000000194 fatty acid Substances 0.000 description 2
229930195729 fatty acid Natural products 0.000 description 2
150000004665 fatty acids Chemical class 0.000 description 2
239000004615 ingredient Substances 0.000 description 2
238000002347 injection Methods 0.000 description 2
239000007924 injection Substances 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
150000003951 lactams Chemical class 0.000 description 2
229920003145 methacrylic acid copolymer Polymers 0.000 description 2
239000002667 nucleating agent Substances 0.000 description 2
WLJVNTCWHIRURA-UHFFFAOYSA-N pimelic acid Chemical compound OC(=O)CCCCCC(O)=O WLJVNTCWHIRURA-UHFFFAOYSA-N 0.000 description 2
238000006116 polymerization reaction Methods 0.000 description 2
239000000843 powder Substances 0.000 description 2
239000000047 product Substances 0.000 description 2
CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 2
TYFQFVWCELRYAO-UHFFFAOYSA-N suberic acid Chemical compound OC(=O)CCCCCCC(O)=O TYFQFVWCELRYAO-UHFFFAOYSA-N 0.000 description 2
238000012360 testing method Methods 0.000 description 2
QHGNHLZPVBIIPX-UHFFFAOYSA-N tin(ii) oxide Chemical compound [Sn]=O QHGNHLZPVBIIPX-UHFFFAOYSA-N 0.000 description 2
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
CFQZKFWQLAHGSL-FNTYJUCDSA-N (3e,5e,7e,9e,11e,13e,15e,17e)-18-[(3e,5e,7e,9e,11e,13e,15e,17e)-18-[(3e,5e,7e,9e,11e,13e,15e)-octadeca-3,5,7,9,11,13,15,17-octaenoyl]oxyoctadeca-3,5,7,9,11,13,15,17-octaenoyl]oxyoctadeca-3,5,7,9,11,13,15,17-octaenoic acid Chemical compound OC(=O)C\C=C\C=C\C=C\C=C\C=C\C=C\C=C\C=C\OC(=O)C\C=C\C=C\C=C\C=C\C=C\C=C\C=C\C=C\OC(=O)C\C=C\C=C\C=C\C=C\C=C\C=C\C=C\C=C CFQZKFWQLAHGSL-FNTYJUCDSA-N 0.000 description 1
RTBFRGCFXZNCOE-UHFFFAOYSA-N 1-methylsulfonylpiperidin-4-one Chemical compound CS(=O)(=O)N1CCC(=O)CC1 RTBFRGCFXZNCOE-UHFFFAOYSA-N 0.000 description 1
QFGCFKJIPBRJGM-UHFFFAOYSA-N 12-[(2-methylpropan-2-yl)oxy]-12-oxododecanoic acid Chemical compound CC(C)(C)OC(=O)CCCCCCCCCCC(O)=O QFGCFKJIPBRJGM-UHFFFAOYSA-N 0.000 description 1
SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
229920006051 Capron® Polymers 0.000 description 1
BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 1
OWYWGLHRNBIFJP-UHFFFAOYSA-N Ipazine Chemical compound CCN(CC)C1=NC(Cl)=NC(NC(C)C)=N1 OWYWGLHRNBIFJP-UHFFFAOYSA-N 0.000 description 1
JHWNWJKBPDFINM-UHFFFAOYSA-N Laurolactam Chemical compound O=C1CCCCCCCCCCCN1 JHWNWJKBPDFINM-UHFFFAOYSA-N 0.000 description 1
239000012963 UV stabilizer Substances 0.000 description 1
239000005083 Zinc sulfide Substances 0.000 description 1
ORLQHILJRHBSAY-UHFFFAOYSA-N [1-(hydroxymethyl)cyclohexyl]methanol Chemical compound OCC1(CO)CCCCC1 ORLQHILJRHBSAY-UHFFFAOYSA-N 0.000 description 1
BGYHLZZASRKEJE-UHFFFAOYSA-N [3-[3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoyloxy]-2,2-bis[3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoyloxymethyl]propyl] 3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoate Chemical compound CC(C)(C)C1=C(O)C(C(C)(C)C)=CC(CCC(=O)OCC(COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)(COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)=C1 BGYHLZZASRKEJE-UHFFFAOYSA-N 0.000 description 1
OCKWAZCWKSMKNC-UHFFFAOYSA-N [3-octadecanoyloxy-2,2-bis(octadecanoyloxymethyl)propyl] octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(COC(=O)CCCCCCCCCCCCCCCCC)(COC(=O)CCCCCCCCCCCCCCCCC)COC(=O)CCCCCCCCCCCCCCCCC OCKWAZCWKSMKNC-UHFFFAOYSA-N 0.000 description 1
YKTSYUJCYHOUJP-UHFFFAOYSA-N [O--].[Al+3].[Al+3].[O-][Si]([O-])([O-])[O-] Chemical compound [O--].[Al+3].[Al+3].[O-][Si]([O-])([O-])[O-] YKTSYUJCYHOUJP-UHFFFAOYSA-N 0.000 description 1
230000002053 acidogenic effect Effects 0.000 description 1
230000000996 additive effect Effects 0.000 description 1
150000001336 alkenes Chemical group 0.000 description 1
150000001408 amides Chemical class 0.000 description 1
230000001034 aminogenic effect Effects 0.000 description 1
JFCQEDHGNNZCLN-UHFFFAOYSA-N anhydrous glutaric acid Natural products OC(=O)CCCC(O)=O JFCQEDHGNNZCLN-UHFFFAOYSA-N 0.000 description 1
239000003963 antioxidant agent Substances 0.000 description 1
239000004760 aramid Substances 0.000 description 1
229920006231 aramid fiber Polymers 0.000 description 1
150000001491 aromatic compounds Chemical class 0.000 description 1
239000010425 asbestos Substances 0.000 description 1
239000011324 bead Substances 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
CDQSJQSWAWPGKG-UHFFFAOYSA-N butane-1,1-diol Chemical compound CCCC(O)O CDQSJQSWAWPGKG-UHFFFAOYSA-N 0.000 description 1
150000004649 carbonic acid derivatives Chemical class 0.000 description 1
150000001734 carboxylic acid salts Chemical class 0.000 description 1
150000001805 chlorine compounds Chemical class 0.000 description 1
125000001309 chloro group Chemical group Cl* 0.000 description 1
239000003086 colorant Substances 0.000 description 1
230000005494 condensation Effects 0.000 description 1
239000007859 condensation product Substances 0.000 description 1
238000005520 cutting process Methods 0.000 description 1
238000000354 decomposition reaction Methods 0.000 description 1
230000000368 destabilizing effect Effects 0.000 description 1
150000001991 dicarboxylic acids Chemical class 0.000 description 1
238000006471 dimerization reaction Methods 0.000 description 1
150000002009 diols Chemical class 0.000 description 1
230000000694 effects Effects 0.000 description 1
230000002708 enhancing effect Effects 0.000 description 1
239000000835 fiber Substances 0.000 description 1
229910052731 fluorine Inorganic materials 0.000 description 1
239000011521 glass Substances 0.000 description 1
239000010439 graphite Substances 0.000 description 1
229910002804 graphite Inorganic materials 0.000 description 1
239000012760 heat stabilizer Substances 0.000 description 1
125000004836 hexamethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[*:1] 0.000 description 1
229920001519 homopolymer Polymers 0.000 description 1
229910052806 inorganic carbonate Inorganic materials 0.000 description 1
229910052809 inorganic oxide Inorganic materials 0.000 description 1
239000011872 intimate mixture Substances 0.000 description 1
229910052740 iodine Inorganic materials 0.000 description 1
229920000554 ionomer Polymers 0.000 description 1
150000002576 ketones Chemical class 0.000 description 1
238000005259 measurement Methods 0.000 description 1
238000010128 melt processing Methods 0.000 description 1
229940117841 methacrylic acid copolymer Drugs 0.000 description 1
RTWNYYOXLSILQN-UHFFFAOYSA-N methanediamine Chemical compound NCN RTWNYYOXLSILQN-UHFFFAOYSA-N 0.000 description 1
239000010445 mica Substances 0.000 description 1
229910052618 mica group Inorganic materials 0.000 description 1
238000002156 mixing Methods 0.000 description 1
239000006082 mold release agent Substances 0.000 description 1
MEFBJEMVZONFCJ-UHFFFAOYSA-N molybdate Chemical compound [O-][Mo]([O-])(=O)=O MEFBJEMVZONFCJ-UHFFFAOYSA-N 0.000 description 1
229910000476 molybdenum oxide Inorganic materials 0.000 description 1
238000006386 neutralization reaction Methods 0.000 description 1
150000002825 nitriles Chemical class 0.000 description 1
229910052757 nitrogen Inorganic materials 0.000 description 1
238000010899 nucleation Methods 0.000 description 1
230000006911 nucleation Effects 0.000 description 1
150000002896 organic halogen compounds Chemical class 0.000 description 1
CABDEMAGSHRORS-UHFFFAOYSA-N oxirane;hydrate Chemical compound O.C1CO1 CABDEMAGSHRORS-UHFFFAOYSA-N 0.000 description 1
PQQKPALAQIIWST-UHFFFAOYSA-N oxomolybdenum Chemical compound [Mo]=O PQQKPALAQIIWST-UHFFFAOYSA-N 0.000 description 1
125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 description 1
229920000233 poly(alkylene oxides) Polymers 0.000 description 1
229920006122 polyamide resin Polymers 0.000 description 1
229920001225 polyester resin Polymers 0.000 description 1
239000004645 polyester resin Substances 0.000 description 1
229910052700 potassium Inorganic materials 0.000 description 1
239000011591 potassium Substances 0.000 description 1
159000000001 potassium salts Chemical class 0.000 description 1
230000001737 promoting effect Effects 0.000 description 1
238000010791 quenching Methods 0.000 description 1
230000000171 quenching effect Effects 0.000 description 1
239000012744 reinforcing agent Substances 0.000 description 1
239000012763 reinforcing filler Substances 0.000 description 1
229910052895 riebeckite Inorganic materials 0.000 description 1
238000007142 ring opening reaction Methods 0.000 description 1
229940124530 sulfonamide Drugs 0.000 description 1
150000003456 sulfonamides Chemical class 0.000 description 1
150000003457 sulfones Chemical class 0.000 description 1
150000003462 sulfoxides Chemical class 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
239000012745 toughening agent Substances 0.000 description 1
239000013638 trimer Chemical class 0.000 description 1
238000005829 trimerization reaction Methods 0.000 description 1
BIKXLKXABVUSMH-UHFFFAOYSA-N trizinc;diborate Chemical compound [Zn+2].[Zn+2].[Zn+2].[O-]B([O-])[O-].[O-]B([O-])[O-] BIKXLKXABVUSMH-UHFFFAOYSA-N 0.000 description 1
239000011787 zinc oxide Substances 0.000 description 1
229910052984 zinc sulfide Inorganic materials 0.000 description 1
DRDVZXDWVBGGMH-UHFFFAOYSA-N zinc;sulfide Chemical compound [S-2].[Zn+2] DRDVZXDWVBGGMH-UHFFFAOYSA-N 0.000 description 1

Landscapes

Compositions Of Macromolecular Compounds (AREA)

JP62271965A 1986-11-26 1987-10-29 ポリエチレンテレフタレート成形混合物 Granted JPS63137952A (ja)

Applications Claiming Priority (3)

Application Number	Priority Date	Filing Date
US93538486A	1986-11-26	1986-11-26
US935384		1986-11-26
US941791		1986-12-15

Publications (2)

Publication Number	Publication Date
JPS63137952A JPS63137952A (ja)	1988-06-09
JPH0478652B2 true JPH0478652B2 (de)	1992-12-11

Family

ID=25467022

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP62271965A Granted JPS63137952A (ja)	1986-11-26	1987-10-29	ポリエチレンテレフタレート成形混合物

Country Status (1)

Country	Link
JP (1)	JPS63137952A (de)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPH0243253A (ja) *	1988-08-03	1990-02-13	Kanegafuchi Chem Ind Co Ltd	射出成形用難燃性ポリエステル系樹脂組成物

1987
- 1987-10-29 JP JP62271965A patent/JPS63137952A/ja active Granted

Also Published As

Publication number	Publication date
JPS63137952A (ja)	1988-06-09

Publication	Publication Date	Title
US4554320A (en)	1985-11-19	Nylon molding materials having high impact strength
AU658436B2 (en)	1995-04-13	Stabilization of polyesters using epoxy compounds in combination with a catalyst
US4401792A (en)	1983-08-30	Process for increasing the rate of crystallization of polyesters
US5034450A (en)	1991-07-23	Thermoplastic molding materials based on polyamides and polyester elastomers
US7105591B2 (en)	2006-09-12	Blends of polyarylether sulphone and polyamide, with improved viscosity and flowability
EP1165692B1 (de)	2006-01-25	Polyester formmasse
JPH0343305B2 (de)	1991-07-02
US4123415A (en)	1978-10-31	Reinforced thermoplastic polyester compositions having improved resistance to heat deflection
US4483949A (en)	1984-11-20	Polyethylene terephthalate blends
EP0404798A1 (de)	1991-01-02	Poly(1,4-cyclohexylendimethylenterephthalat)-giesszusammensetzungen
US5028649A (en)	1991-07-02	Polyethylene terephthalate molding compounds with sodium stearate and polyester amides
US4866115A (en)	1989-09-12	Solid mixture of nucleated and nonnucleated polyamides
US4229340A (en)	1980-10-21	Glass fiber-reinforced polyethylene terephthalate/polyamide blends
JPS6057464B2 (ja)	1985-12-14	ポリアミド樹脂組成物
EP0388518A2 (de)	1990-09-26	Polyethylenterephthalat-Formmassen
CA1104734A (en)	1981-07-07	Unfilled thermoplastic molding compositions
KR910003507B1 (ko)	1991-06-03	방염성 폴리에틸렌 테레프탈레이트
US5068274A (en)	1991-11-26	Secondary amides in polyethylene terephthalate molding compositions
US5015681A (en)	1991-05-14	Flameproof thermoplastic molding materials based on polyamides and polyester elastomers
JPH0478652B2 (de)	1992-12-11
EP0020739B1 (de)	1985-03-13	Thermoplastische formmassen
JPH05506056A (ja)	1993-09-02	溶融粘度の高い充填材含有ポリエステル組成物
JPS60226549A (ja)	1985-11-11	成型組成物
JPH0395265A (ja)	1991-04-19	樹脂組成物
JPH0254384B2 (de)	1990-11-21

Legal Events

Date	Code	Title	Description
2007-10-29	EXPY	Cancellation because of completion of term