NL8901880A - Anisotrope polymeren op basis van een s-triazinederivaat. - Google Patents

Anisotrope polymeren op basis van een s-triazinederivaat. Download PDF

Info

Publication number: NL8901880A
Authority: NL; Netherlands
Prior art keywords: polymer; mol; polymer according; unit; aromatic
Prior art date: 1989-07-20

Application number

NL8901880A

Other languages

English (en)

Dutch (nl)

Original Assignee

Stamicarbon

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.)

1989-07-20

Filing date

1989-07-20

Publication date

1991-02-18

1989-07-20 Application filed by Stamicarbon filed Critical Stamicarbon

1989-07-20 Priority to NL8901880A priority Critical patent/NL8901880A/nl

1990-07-16 Priority to EP19900201918 priority patent/EP0409334A3/en

1990-07-20 Priority to JP19283090A priority patent/JPH0381322A/ja

1991-02-18 Publication of NL8901880A publication Critical patent/NL8901880A/nl

Links

229920000642 polymer Polymers 0.000 title claims description 64
JIHQDMXYYFUGFV-UHFFFAOYSA-N 1,3,5-triazine Chemical class C1=NC=NC=N1 JIHQDMXYYFUGFV-UHFFFAOYSA-N 0.000 title description 3
125000003118 aryl group Chemical group 0.000 claims description 21
-1 aromatic hydroxy acids Chemical class 0.000 claims description 16
JYEUMXHLPRZUAT-UHFFFAOYSA-N 1,2,3-triazine Chemical group C1=CN=NN=C1 JYEUMXHLPRZUAT-UHFFFAOYSA-N 0.000 claims description 13
JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine powder Natural products NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 claims description 11
125000000217 alkyl group Chemical group 0.000 claims description 7
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 7
229920000877 Melamine resin Polymers 0.000 claims description 6
GZVHEAJQGPRDLQ-UHFFFAOYSA-N 6-phenyl-1,3,5-triazine-2,4-diamine Chemical compound NC1=NC(N)=NC(C=2C=CC=CC=2)=N1 GZVHEAJQGPRDLQ-UHFFFAOYSA-N 0.000 claims description 5
NJYZCEFQAIUHSD-UHFFFAOYSA-N acetoguanamine Chemical group CC1=NC(N)=NC(N)=N1 NJYZCEFQAIUHSD-UHFFFAOYSA-N 0.000 claims description 5
125000004432 carbon atom Chemical group C* 0.000 claims description 5
229910052736 halogen Inorganic materials 0.000 claims description 5
150000002367 halogens Chemical class 0.000 claims description 5
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 5
125000003277 amino group Chemical group 0.000 claims description 4
239000000835 fiber Substances 0.000 claims description 4
FALRKNHUBBKYCC-UHFFFAOYSA-N 2-(chloromethyl)pyridine-3-carbonitrile Chemical compound ClCC1=NC=CC=C1C#N FALRKNHUBBKYCC-UHFFFAOYSA-N 0.000 claims description 3
239000001257 hydrogen Substances 0.000 claims description 3
229910052739 hydrogen Inorganic materials 0.000 claims description 3
239000000178 monomer Substances 0.000 claims description 3
229940014800 succinic anhydride Drugs 0.000 claims description 3
LGRFSURHDFAFJT-UHFFFAOYSA-N Phthalic anhydride Natural products C1=CC=C2C(=O)OC(=O)C2=C1 LGRFSURHDFAFJT-UHFFFAOYSA-N 0.000 claims description 2
RMRFFCXPLWYOOY-UHFFFAOYSA-N allyl radical Chemical compound [CH2]C=C RMRFFCXPLWYOOY-UHFFFAOYSA-N 0.000 claims description 2
150000005840 aryl radicals Chemical class 0.000 claims description 2
JHIWVOJDXOSYLW-UHFFFAOYSA-N butyl 2,2-difluorocyclopropane-1-carboxylate Chemical compound CCCCOC(=O)C1CC1(F)F JHIWVOJDXOSYLW-UHFFFAOYSA-N 0.000 claims description 2
125000005157 alkyl carboxy group Chemical group 0.000 claims 1
125000002887 hydroxy group Chemical group [H]O* 0.000 claims 1
239000000155 melt Substances 0.000 claims 1
FJKROLUGYXJWQN-UHFFFAOYSA-N 4-hydroxybenzoic acid Chemical compound OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 19
KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 19
QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 14
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 10
229940090248 4-hydroxybenzoic acid Drugs 0.000 description 9
WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 9
QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 8
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 8
230000035939 shock Effects 0.000 description 8
235000013904 zinc acetate Nutrition 0.000 description 7
ZOIORXHNWRGPMV-UHFFFAOYSA-N acetic acid;zinc Chemical compound [Zn].CC(O)=O.CC(O)=O ZOIORXHNWRGPMV-UHFFFAOYSA-N 0.000 description 6
238000006243 chemical reaction Methods 0.000 description 6
238000002844 melting Methods 0.000 description 6
230000008018 melting Effects 0.000 description 6
238000010992 reflux Methods 0.000 description 6
239000004246 zinc acetate Substances 0.000 description 6
229910052757 nitrogen Inorganic materials 0.000 description 5
125000001820 oxy group Chemical group [*:1]O[*:2] 0.000 description 5
238000000113 differential scanning calorimetry Methods 0.000 description 4
238000006467 substitution reaction Methods 0.000 description 4
KAUQJMHLAFIZDU-UHFFFAOYSA-N 6-Hydroxy-2-naphthoic acid Chemical compound C1=C(O)C=CC2=CC(C(=O)O)=CC=C21 KAUQJMHLAFIZDU-UHFFFAOYSA-N 0.000 description 3
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 3
125000003545 alkoxy group Chemical group 0.000 description 3
230000000052 comparative effect Effects 0.000 description 3
150000001875 compounds Chemical class 0.000 description 3
239000000203 mixture Substances 0.000 description 3
239000000126 substance Substances 0.000 description 3
FJSKXQVRKZTKSI-UHFFFAOYSA-N 2,3-dimethylfuran Chemical compound CC=1C=COC=1C FJSKXQVRKZTKSI-UHFFFAOYSA-N 0.000 description 2
ALYNCZNDIQEVRV-UHFFFAOYSA-N 4-aminobenzoic acid Chemical compound NC1=CC=C(C(O)=O)C=C1 ALYNCZNDIQEVRV-UHFFFAOYSA-N 0.000 description 2
PLIKAWJENQZMHA-UHFFFAOYSA-N 4-aminophenol Chemical compound NC1=CC=C(O)C=C1 PLIKAWJENQZMHA-UHFFFAOYSA-N 0.000 description 2
XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
150000008064 anhydrides Chemical class 0.000 description 2
239000003054 catalyst Substances 0.000 description 2
238000004821 distillation Methods 0.000 description 2
YBMRDBCBODYGJE-UHFFFAOYSA-N germanium dioxide Chemical compound O=[Ge]=O YBMRDBCBODYGJE-UHFFFAOYSA-N 0.000 description 2
235000011285 magnesium acetate Nutrition 0.000 description 2
238000004519 manufacturing process Methods 0.000 description 2
238000000034 method Methods 0.000 description 2
238000006116 polymerization reaction Methods 0.000 description 2
SCVFZCLFOSHCOH-UHFFFAOYSA-M potassium acetate Chemical compound [K+].CC([O-])=O SCVFZCLFOSHCOH-UHFFFAOYSA-M 0.000 description 2
229920005989 resin Polymers 0.000 description 2
239000011347 resin Substances 0.000 description 2
239000000243 solution Substances 0.000 description 2
KDYFGRWQOYBRFD-UHFFFAOYSA-N succinic acid Chemical compound OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 2
239000000725 suspension Substances 0.000 description 2
150000003918 triazines Chemical class 0.000 description 2
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 description 1
CBCKQZAAMUWICA-UHFFFAOYSA-N 1,4-phenylenediamine Chemical compound NC1=CC=C(N)C=C1 CBCKQZAAMUWICA-UHFFFAOYSA-N 0.000 description 1
PVRZMTHMPKVOBP-UHFFFAOYSA-N 1-n,4-n-dimethylbenzene-1,4-diamine Chemical compound CNC1=CC=C(NC)C=C1 PVRZMTHMPKVOBP-UHFFFAOYSA-N 0.000 description 1
LVVXLDUCGFTWHJ-UHFFFAOYSA-N 2,2-diphenylbutanedioic acid Chemical compound C=1C=CC=CC=1C(C(O)=O)(CC(=O)O)C1=CC=CC=C1 LVVXLDUCGFTWHJ-UHFFFAOYSA-N 0.000 description 1
229940075142 2,5-diaminotoluene Drugs 0.000 description 1
OBCSAIDCZQSFQH-UHFFFAOYSA-N 2-methyl-1,4-phenylenediamine Chemical compound CC1=CC(N)=CC=C1N OBCSAIDCZQSFQH-UHFFFAOYSA-N 0.000 description 1
125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
ICNFHJVPAJKPHW-UHFFFAOYSA-N 4,4'-Thiodianiline Chemical compound C1=CC(N)=CC=C1SC1=CC=C(N)C=C1 ICNFHJVPAJKPHW-UHFFFAOYSA-N 0.000 description 1
YBRVSVVVWCFQMG-UHFFFAOYSA-N 4,4'-diaminodiphenylmethane Chemical compound C1=CC(N)=CC=C1CC1=CC=C(N)C=C1 YBRVSVVVWCFQMG-UHFFFAOYSA-N 0.000 description 1
PSHPCZGANRRQDN-UHFFFAOYSA-N 4-(4-aminophenyl)sulfonylphenol Chemical compound C1=CC(N)=CC=C1S(=O)(=O)C1=CC=C(O)C=C1 PSHPCZGANRRQDN-UHFFFAOYSA-N 0.000 description 1
HLBLWEWZXPIGSM-UHFFFAOYSA-N 4-Aminophenyl ether Chemical compound C1=CC(N)=CC=C1OC1=CC=C(N)C=C1 HLBLWEWZXPIGSM-UHFFFAOYSA-N 0.000 description 1
XKACUVXWRVMXOE-UHFFFAOYSA-N 4-[2-(4-carboxyphenyl)propan-2-yl]benzoic acid Chemical compound C=1C=C(C(O)=O)C=CC=1C(C)(C)C1=CC=C(C(O)=O)C=C1 XKACUVXWRVMXOE-UHFFFAOYSA-N 0.000 description 1
ABJQKDJOYSQVFX-UHFFFAOYSA-N 4-aminonaphthalen-1-ol Chemical compound C1=CC=C2C(N)=CC=C(O)C2=C1 ABJQKDJOYSQVFX-UHFFFAOYSA-N 0.000 description 1
VVYWUQOTMZEJRJ-UHFFFAOYSA-N 4-n-methylbenzene-1,4-diamine Chemical compound CNC1=CC=C(N)C=C1 VVYWUQOTMZEJRJ-UHFFFAOYSA-N 0.000 description 1
239000005995 Aluminium silicate Substances 0.000 description 1
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
BMTAFVWTTFSTOG-UHFFFAOYSA-N Butylate Chemical compound CCSC(=O)N(CC(C)C)CC(C)C BMTAFVWTTFSTOG-UHFFFAOYSA-N 0.000 description 1
BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
235000008733 Citrus aurantifolia Nutrition 0.000 description 1
229920001634 Copolyester Polymers 0.000 description 1
MQJKPEGWNLWLTK-UHFFFAOYSA-N Dapsone Chemical compound C1=CC(N)=CC=C1S(=O)(=O)C1=CC=C(N)C=C1 MQJKPEGWNLWLTK-UHFFFAOYSA-N 0.000 description 1
JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
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
229930194542 Keto Natural products 0.000 description 1
FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
239000004952 Polyamide Substances 0.000 description 1
239000004743 Polypropylene Substances 0.000 description 1
VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 description 1
235000011941 Tilia x europaea Nutrition 0.000 description 1
230000021736 acetylation Effects 0.000 description 1
238000006640 acetylation reaction Methods 0.000 description 1
239000002253 acid Substances 0.000 description 1
150000008065 acid anhydrides Chemical class 0.000 description 1
239000000853 adhesive Substances 0.000 description 1
230000001070 adhesive effect Effects 0.000 description 1
235000012211 aluminium silicate Nutrition 0.000 description 1
150000001412 amines Chemical class 0.000 description 1
229960004050 aminobenzoic acid Drugs 0.000 description 1
229910052786 argon Inorganic materials 0.000 description 1
238000003556 assay Methods 0.000 description 1
125000000751 azo group Chemical group [*]N=N[*] 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
229910052794 bromium Inorganic materials 0.000 description 1
VSGNNIFQASZAOI-UHFFFAOYSA-L calcium acetate Chemical compound [Ca+2].CC([O-])=O.CC([O-])=O VSGNNIFQASZAOI-UHFFFAOYSA-L 0.000 description 1
239000001639 calcium acetate Substances 0.000 description 1
235000011092 calcium acetate Nutrition 0.000 description 1
229960005147 calcium acetate Drugs 0.000 description 1
239000004301 calcium benzoate Substances 0.000 description 1
235000010237 calcium benzoate Nutrition 0.000 description 1
HZQXCUSDXIKLGS-UHFFFAOYSA-L calcium;dibenzoate;trihydrate Chemical compound O.O.O.[Ca+2].[O-]C(=O)C1=CC=CC=C1.[O-]C(=O)C1=CC=CC=C1 HZQXCUSDXIKLGS-UHFFFAOYSA-L 0.000 description 1
239000000460 chlorine Substances 0.000 description 1
229910052801 chlorine Inorganic materials 0.000 description 1
239000011248 coating agent Substances 0.000 description 1
238000000576 coating method Methods 0.000 description 1
229940011182 cobalt acetate Drugs 0.000 description 1
QAHREYKOYSIQPH-UHFFFAOYSA-L cobalt(II) acetate Chemical compound [Co+2].CC([O-])=O.CC([O-])=O QAHREYKOYSIQPH-UHFFFAOYSA-L 0.000 description 1
238000009833 condensation Methods 0.000 description 1
230000005494 condensation Effects 0.000 description 1
238000001816 cooling Methods 0.000 description 1
238000000354 decomposition reaction Methods 0.000 description 1
230000003247 decreasing effect Effects 0.000 description 1
230000001419 dependent effect Effects 0.000 description 1
ZXDVQYBUEVYUCG-UHFFFAOYSA-N dibutyltin(2+);methanolate Chemical compound CCCC[Sn](OC)(OC)CCCC ZXDVQYBUEVYUCG-UHFFFAOYSA-N 0.000 description 1
239000012153 distilled water Substances 0.000 description 1
238000004870 electrical engineering Methods 0.000 description 1
230000032050 esterification Effects 0.000 description 1
238000005886 esterification reaction Methods 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
238000001125 extrusion Methods 0.000 description 1
239000000945 filler Substances 0.000 description 1
229910052731 fluorine Inorganic materials 0.000 description 1
239000011737 fluorine Substances 0.000 description 1
125000000524 functional group Chemical group 0.000 description 1
229940119177 germanium dioxide Drugs 0.000 description 1
239000003365 glass fiber Substances 0.000 description 1
150000002391 heterocyclic compounds Chemical class 0.000 description 1
125000004356 hydroxy functional group Chemical group O* 0.000 description 1
150000003949 imides Chemical class 0.000 description 1
238000001746 injection moulding Methods 0.000 description 1
NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
125000000468 ketone group Chemical group 0.000 description 1
239000004571 lime Substances 0.000 description 1
XIXADJRWDQXREU-UHFFFAOYSA-M lithium acetate Chemical compound [Li+].CC([O-])=O XIXADJRWDQXREU-UHFFFAOYSA-M 0.000 description 1
239000011777 magnesium Substances 0.000 description 1
229910052749 magnesium Inorganic materials 0.000 description 1
UEGPKNKPLBYCNK-UHFFFAOYSA-L magnesium acetate Chemical compound [Mg+2].CC([O-])=O.CC([O-])=O UEGPKNKPLBYCNK-UHFFFAOYSA-L 0.000 description 1
239000011654 magnesium acetate Substances 0.000 description 1
229940069446 magnesium acetate Drugs 0.000 description 1
AKTIAGQCYPCKFX-FDGPNNRMSA-L magnesium;(z)-4-oxopent-2-en-2-olate Chemical compound [Mg+2].C\C([O-])=C\C(C)=O.C\C([O-])=C\C(C)=O AKTIAGQCYPCKFX-FDGPNNRMSA-L 0.000 description 1
239000000463 material Substances 0.000 description 1
238000010128 melt processing Methods 0.000 description 1
RXOHFPCZGPKIRD-UHFFFAOYSA-N naphthalene-2,6-dicarboxylic acid Chemical compound C1=C(C(O)=O)C=CC2=CC(C(=O)O)=CC=C21 RXOHFPCZGPKIRD-UHFFFAOYSA-N 0.000 description 1
WPUMVKJOWWJPRK-UHFFFAOYSA-N naphthalene-2,7-dicarboxylic acid Chemical compound C1=CC(C(O)=O)=CC2=CC(C(=O)O)=CC=C21 WPUMVKJOWWJPRK-UHFFFAOYSA-N 0.000 description 1
238000004806 packaging method and process Methods 0.000 description 1
229920002647 polyamide Polymers 0.000 description 1
229920001707 polybutylene terephthalate Polymers 0.000 description 1
238000006068 polycondensation reaction Methods 0.000 description 1
229920000728 polyester Polymers 0.000 description 1
229920001155 polypropylene Polymers 0.000 description 1
235000011056 potassium acetate Nutrition 0.000 description 1
238000002360 preparation method Methods 0.000 description 1
239000011734 sodium Substances 0.000 description 1
229910052708 sodium Inorganic materials 0.000 description 1
239000001632 sodium acetate Substances 0.000 description 1
235000017281 sodium acetate Nutrition 0.000 description 1
238000003756 stirring Methods 0.000 description 1
125000001424 substituent group Chemical class 0.000 description 1
239000001384 succinic acid Substances 0.000 description 1
238000003786 synthesis reaction Methods 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 0.000 description 1
150000003504 terephthalic acids Chemical class 0.000 description 1
239000004753 textile Substances 0.000 description 1
229920001169 thermoplastic Polymers 0.000 description 1
239000004416 thermosoftening plastic Substances 0.000 description 1
150000007970 thio esters Chemical group 0.000 description 1
229910001887 tin oxide Inorganic materials 0.000 description 1
UOCLRXFKRLRMKV-UHFFFAOYSA-N trolnitrate phosphate Chemical compound OP(O)(O)=O.OP(O)(O)=O.[O-][N+](=O)OCCN(CCO[N+]([O-])=O)CCO[N+]([O-])=O UOCLRXFKRLRMKV-UHFFFAOYSA-N 0.000 description 1
239000010456 wollastonite Substances 0.000 description 1
229910052882 wollastonite Inorganic materials 0.000 description 1
DJWUNCQRNNEAKC-UHFFFAOYSA-L zinc acetate Chemical class [Zn+2].CC([O-])=O.CC([O-])=O DJWUNCQRNNEAKC-UHFFFAOYSA-L 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
- C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
- C08G63/68—Polyesters containing atoms other than carbon, hydrogen and oxygen
- C08G63/685—Polyesters containing atoms other than carbon, hydrogen and oxygen containing nitrogen
- 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
- C08G69/44—Polyester-amides

Landscapes

Chemical & Material Sciences (AREA)
Health & Medical Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Organic Chemistry (AREA)
Polyesters Or Polycarbonates (AREA)
Polyamides (AREA)
Manufacture Of Macromolecular Shaped Articles (AREA)
Fireproofing Substances (AREA)
Artificial Filaments (AREA)

NL8901880A 1989-07-20 1989-07-20 Anisotrope polymeren op basis van een s-triazinederivaat. NL8901880A (nl)

Priority Applications (3)

Application Number	Priority Date	Filing Date	Title
NL8901880A NL8901880A (nl)	1989-07-20	1989-07-20	Anisotrope polymeren op basis van een s-triazinederivaat.
EP19900201918 EP0409334A3 (en)	1989-07-20	1990-07-16	Anisotropic polymers based on an s-triazine derivative
JP19283090A JPH0381322A (ja)	1989-07-20	1990-07-20	ｓ‐トリアジン誘導体に基づく異方性ポリマー

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
NL8901880		1989-07-20
NL8901880A NL8901880A (nl)	1989-07-20	1989-07-20	Anisotrope polymeren op basis van een s-triazinederivaat.

Publications (1)

Publication Number	Publication Date
NL8901880A true NL8901880A (nl)	1991-02-18

Family

ID=19855075

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NL8901880A NL8901880A (nl)	1989-07-20	1989-07-20	Anisotrope polymeren op basis van een s-triazinederivaat.

Country Status (3)

Country	Link
EP (1)	EP0409334A3 (fr)
JP (1)	JPH0381322A (fr)
NL (1)	NL8901880A (fr)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
BE1006449A3 (nl) *	1992-12-15	1994-08-30	Dsm Nv	Melaminederivaat.

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
BR9707817A (pt) *	1996-03-01	1999-07-27	Cytec Tech Corp	Composto composiçao curável substrato revestido como proteção processo para preparar um composto e pré-polímero
AU2004256008B2 (en) *	2003-02-27	2009-10-29	Steven W. Fowkes	Aromatic amide polymer systems and methods for making the same
US20090198039A1 (en) *	2005-11-17	2009-08-06	Berg Van Den Hendrik J	Process for the preparation of a polymer having improved dyeability
JP6247915B2 (ja) *	2013-12-03	2017-12-13	株式会社クラレ	耐候性を有するサーモトロピック液晶ポリマーおよび成形品

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE1495141A1 (de) *	1963-09-14	1969-03-27	Basf Ag	Verfahren zum Herstellen von Triazinringe enthaltenden Polymeren
JPH0768345B2 (ja) *	1987-02-10	1995-07-26	三菱レイヨン株式会社	共重合ポリエステル樹脂の製造方法
DE3704877A1 (de) *	1987-02-17	1988-08-25	Merck Patent Gmbh	Fluessigkristalline phasen aufweisende polymermaterialien
NL8803182A (nl) *	1988-12-28	1990-07-16	Stamicarbon	Uit de smelt verwerkbaar polymeer.

1989
- 1989-07-20 NL NL8901880A patent/NL8901880A/nl not_active Application Discontinuation
1990
- 1990-07-16 EP EP19900201918 patent/EP0409334A3/en not_active Withdrawn
- 1990-07-20 JP JP19283090A patent/JPH0381322A/ja active Pending

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
BE1006449A3 (nl) *	1992-12-15	1994-08-30	Dsm Nv	Melaminederivaat.

Also Published As

Publication number	Publication date
EP0409334A3 (en)	1991-06-26
EP0409334A2 (fr)	1991-01-23
JPH0381322A (ja)	1991-04-05

Legal Events

Date	Code	Title	Description
1991-02-18	A1B	A search report has been drawn up
1992-03-02	BV	The patent application has lapsed

Publication	Publication Date	Title
US3637595A (en)	1972-01-25	P-oxybenzoyl copolyesters
US5616680A (en)	1997-04-01	Process for producing liquid crystal polymer
CA1335225C (fr)	1995-04-11	Polyester et article fabrique avec materiau
EP0323710A1 (fr)	1989-07-12	Polyesters liquides cristallins, aromatiques et thermotropiques
US5134201A (en)	1992-07-28	Miscible polyester blends
NL8901880A (nl)	1991-02-18	Anisotrope polymeren op basis van een s-triazinederivaat.
EP0376380A1 (fr)	1990-07-04	Polymère transformable à l'état fondu
JP3913527B2 (ja)	2007-05-09	全芳香族ポリエステルアミド及びポリエステルアミド樹脂組成物
US5049643A (en)	1991-09-17	Wholly aromatic polyester from mixture of naphthalene dicarboxylic acid
EP0493077A2 (fr)	1992-07-01	Résine de polyester moulable ayant une grande stabilité à la chaleur de fusion et produits de moulage ainsi obtenus
US5051490A (en)	1991-09-24	Thermoplastic polyarylate compositions having improved oxygen barrier properties
US5183878A (en)	1993-02-02	Easily processable, wholly aromatic polyester
US4988776A (en)	1991-01-29	Polymer composition on the basis of polymer and a polyester amide
US5102978A (en)	1992-04-07	Copolyester
EP0747415A2 (fr)	1996-12-11	Procédé de préparation de polymère crystallin liquide
CA1101596A (fr)	1981-05-19	Traduction non-disponible
NL8901679A (nl)	1991-02-01	Aromatisch polymeer met diaminoanthrachinon eenheden.
US4978735A (en)	1990-12-18	Thermotropic liquid crystalline aromatic polyester from 3,3'-diphenyl-4,4'-d
KR970010754B1 (ko)	1997-06-30	액정 열호변성 방향족 폴리에스테르
EP0321107B1 (fr)	1995-01-25	Polyesters liquides cristallins, aromatiques et thermotropiques
NL8901535A (nl)	1991-01-16	Polymeersamenstelling.
JPH03255124A (ja)	1991-11-14	芳香族ポリエステルアミド共重合体およびその製造法
JPH0420526A (ja)	1992-01-24	芳香族ポリエステルアミドの製造法
US4966957A (en)	1990-10-30	Liquid-crystalline, thermotropic aromatic polyester from hydroquinone mixture
JPH02629A (ja)	1990-01-05	スピロビインダンポリアリーレートーポリエステルコポリマー，製造方法

NL8901880A - Anisotrope polymeren op basis van een s-triazinederivaat. - Google Patents

Info

Links

Classifications

Landscapes

Priority Applications (3)

Applications Claiming Priority (2)

Publications (1)

Family

ID=19855075

Family Applications (1)

Country Status (3)

Cited By (1)

Families Citing this family (4)

Family Cites Families (4)

Cited By (1)

Also Published As

Similar Documents

Legal Events