CH650392A5 - Feuerfestes geschirr auf basis eines geformten, gegebenenfalls modifizierten homo- oder copolyesters. - Google Patents
Feuerfestes geschirr auf basis eines geformten, gegebenenfalls modifizierten homo- oder copolyesters. Download PDFInfo
- Publication number
- CH650392A5 CH650392A5 CH6781/80A CH678180A CH650392A5 CH 650392 A5 CH650392 A5 CH 650392A5 CH 6781/80 A CH6781/80 A CH 6781/80A CH 678180 A CH678180 A CH 678180A CH 650392 A5 CH650392 A5 CH 650392A5
- Authority
- CH
- Switzerland
- Prior art keywords
- units
- formula
- acid
- polyesters
- formulas
- Prior art date
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- 229920001634 Copolyester Polymers 0.000 title claims description 9
- 238000004770 highest occupied molecular orbital Methods 0.000 title 1
- 229920000728 polyester Polymers 0.000 claims description 39
- 235000013305 food Nutrition 0.000 claims description 11
- 239000000126 substance Substances 0.000 claims description 11
- 239000004033 plastic Substances 0.000 claims description 10
- 229920003023 plastic Polymers 0.000 claims description 10
- 239000000463 material Substances 0.000 claims description 9
- FJKROLUGYXJWQN-UHFFFAOYSA-N 4-hydroxybenzoic acid Chemical compound OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 claims description 8
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 claims description 8
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 7
- 125000001820 oxy group Chemical group [*:1]O[*:2] 0.000 claims description 7
- 229920002492 poly(sulfone) Polymers 0.000 claims description 7
- 229940090248 4-hydroxybenzoic acid Drugs 0.000 claims description 4
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 claims description 4
- 230000015572 biosynthetic process Effects 0.000 claims description 4
- 238000009835 boiling Methods 0.000 claims description 4
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 claims description 4
- 229920000642 polymer Polymers 0.000 claims description 4
- GDBUZIKSJGRBJP-UHFFFAOYSA-N 4-acetoxy benzoic acid Chemical compound CC(=O)OC1=CC=C(C(O)=O)C=C1 GDBUZIKSJGRBJP-UHFFFAOYSA-N 0.000 claims description 3
- 125000000217 alkyl group Chemical group 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
- 238000003786 synthesis reaction Methods 0.000 claims description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 3
- 239000002253 acid Substances 0.000 claims description 2
- 125000006267 biphenyl group Chemical group 0.000 claims description 2
- 238000010411 cooking Methods 0.000 claims description 2
- HPGJOUYGWKFYQW-UHFFFAOYSA-N diphenyl benzene-1,4-dicarboxylate Chemical compound C=1C=C(C(=O)OC=2C=CC=CC=2)C=CC=1C(=O)OC1=CC=CC=C1 HPGJOUYGWKFYQW-UHFFFAOYSA-N 0.000 claims description 2
- 150000001875 compounds Chemical class 0.000 claims 4
- 229910052739 hydrogen Inorganic materials 0.000 claims 4
- 239000001257 hydrogen Substances 0.000 claims 4
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims 4
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 claims 2
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 2
- 125000001589 carboacyl group Chemical group 0.000 claims 2
- 238000002360 preparation method Methods 0.000 claims 2
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 claims 2
- JTUIDPCUTRXCPW-UHFFFAOYSA-N (6-acetyloxynaphthalen-2-yl) acetate Chemical compound C1=C(OC(C)=O)C=CC2=CC(OC(=O)C)=CC=C21 JTUIDPCUTRXCPW-UHFFFAOYSA-N 0.000 claims 1
- FRASJONUBLZVQX-UHFFFAOYSA-N 1,4-dioxonaphthalene Natural products C1=CC=C2C(=O)C=CC(=O)C2=C1 FRASJONUBLZVQX-UHFFFAOYSA-N 0.000 claims 1
- BOKGTLAJQHTOKE-UHFFFAOYSA-N 1,5-dihydroxynaphthalene Chemical compound C1=CC=C2C(O)=CC=CC2=C1O BOKGTLAJQHTOKE-UHFFFAOYSA-N 0.000 claims 1
- NALNZSALNRPKIG-UHFFFAOYSA-N 2-methylpropyl 4-acetyloxybenzoate Chemical compound CC(C)COC(=O)C1=CC=C(OC(C)=O)C=C1 NALNZSALNRPKIG-UHFFFAOYSA-N 0.000 claims 1
- UFMBOFGKHIXOTA-UHFFFAOYSA-N 2-methylterephthalic acid Chemical compound CC1=CC(C(O)=O)=CC=C1C(O)=O UFMBOFGKHIXOTA-UHFFFAOYSA-N 0.000 claims 1
- RXNYJUSEXLAVNQ-UHFFFAOYSA-N 4,4'-Dihydroxybenzophenone Chemical compound C1=CC(O)=CC=C1C(=O)C1=CC=C(O)C=C1 RXNYJUSEXLAVNQ-UHFFFAOYSA-N 0.000 claims 1
- NZGQHKSLKRFZFL-UHFFFAOYSA-N 4-(4-hydroxyphenoxy)phenol Chemical compound C1=CC(O)=CC=C1OC1=CC=C(O)C=C1 NZGQHKSLKRFZFL-UHFFFAOYSA-N 0.000 claims 1
- WDCVVRPXMOAZLY-UHFFFAOYSA-N 5-acetyloxynaphthalene-1-carboxylic acid Chemical compound C1=CC=C2C(OC(=O)C)=CC=CC2=C1C(O)=O WDCVVRPXMOAZLY-UHFFFAOYSA-N 0.000 claims 1
- JCJUKCIXTRWAQY-UHFFFAOYSA-N 6-hydroxynaphthalene-1-carboxylic acid Chemical compound OC1=CC=C2C(C(=O)O)=CC=CC2=C1 JCJUKCIXTRWAQY-UHFFFAOYSA-N 0.000 claims 1
- 150000007513 acids Chemical class 0.000 claims 1
- 238000005452 bending Methods 0.000 claims 1
- 150000001555 benzenes Chemical class 0.000 claims 1
- 150000001805 chlorine compounds Chemical class 0.000 claims 1
- 229920001577 copolymer Polymers 0.000 claims 1
- 230000001627 detrimental effect Effects 0.000 claims 1
- JLVWYWVLMFVCDI-UHFFFAOYSA-N diethyl benzene-1,3-dicarboxylate Chemical compound CCOC(=O)C1=CC=CC(C(=O)OCC)=C1 JLVWYWVLMFVCDI-UHFFFAOYSA-N 0.000 claims 1
- 230000009970 fire resistant effect Effects 0.000 claims 1
- 150000005165 hydroxybenzoic acids Chemical class 0.000 claims 1
- 238000007654 immersion Methods 0.000 claims 1
- 238000001746 injection moulding Methods 0.000 claims 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 claims 1
- ABMFBCRYHDZLRD-UHFFFAOYSA-N naphthalene-1,4-dicarboxylic acid Chemical compound C1=CC=C2C(C(=O)O)=CC=C(C(O)=O)C2=C1 ABMFBCRYHDZLRD-UHFFFAOYSA-N 0.000 claims 1
- PCILLCXFKWDRMK-UHFFFAOYSA-N naphthalene-1,4-diol Chemical compound C1=CC=C2C(O)=CC=C(O)C2=C1 PCILLCXFKWDRMK-UHFFFAOYSA-N 0.000 claims 1
- DFFZOPXDTCDZDP-UHFFFAOYSA-N naphthalene-1,5-dicarboxylic acid Chemical compound C1=CC=C2C(C(=O)O)=CC=CC2=C1C(O)=O DFFZOPXDTCDZDP-UHFFFAOYSA-N 0.000 claims 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 claims 1
- 125000001624 naphthyl group Chemical group 0.000 claims 1
- GJLNWLVPAHNBQN-UHFFFAOYSA-N phenyl 4-hydroxybenzoate Chemical compound C1=CC(O)=CC=C1C(=O)OC1=CC=CC=C1 GJLNWLVPAHNBQN-UHFFFAOYSA-N 0.000 claims 1
- GUWYYXPNUUACGW-UHFFFAOYSA-N phenyl 5-hydroxynaphthalene-1-carboxylate Chemical compound C1=CC=C2C(O)=CC=CC2=C1C(=O)OC1=CC=CC=C1 GUWYYXPNUUACGW-UHFFFAOYSA-N 0.000 claims 1
- 229920000306 polymethylpentene Polymers 0.000 claims 1
- 239000011116 polymethylpentene Substances 0.000 claims 1
- 230000035939 shock Effects 0.000 claims 1
- 239000000243 solution Substances 0.000 claims 1
- 239000004094 surface-active agent Substances 0.000 claims 1
- -1 chlorine or bromine Chemical class 0.000 description 13
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 12
- 239000000203 mixture Substances 0.000 description 12
- 229920005989 resin Polymers 0.000 description 11
- 239000011347 resin Substances 0.000 description 11
- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 9
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 8
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 8
- 238000010438 heat treatment Methods 0.000 description 7
- 229920001707 polybutylene terephthalate Polymers 0.000 description 6
- 239000000843 powder Substances 0.000 description 6
- 238000010992 reflux Methods 0.000 description 6
- 239000004743 Polypropylene Substances 0.000 description 5
- 238000004821 distillation Methods 0.000 description 5
- 239000007788 liquid Substances 0.000 description 5
- 229920001155 polypropylene Polymers 0.000 description 5
- YJTKZCDBKVTVBY-UHFFFAOYSA-N 1,3-Diphenylbenzene Chemical group C1=CC=CC=C1C1=CC=CC(C=2C=CC=CC=2)=C1 YJTKZCDBKVTVBY-UHFFFAOYSA-N 0.000 description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
- 235000015173 baked goods and baking mixes Nutrition 0.000 description 4
- 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 4
- 238000006243 chemical reaction Methods 0.000 description 4
- 239000011521 glass Substances 0.000 description 4
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 4
- 229910000041 hydrogen chloride Inorganic materials 0.000 description 4
- 229910052757 nitrogen Inorganic materials 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- 239000011541 reaction mixture Substances 0.000 description 4
- 235000015067 sauces Nutrition 0.000 description 4
- 238000003756 stirring Methods 0.000 description 4
- 235000021168 barbecue Nutrition 0.000 description 3
- 238000001816 cooling Methods 0.000 description 3
- 238000002845 discoloration Methods 0.000 description 3
- 239000011551 heat transfer agent Substances 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 229920001187 thermosetting polymer Polymers 0.000 description 3
- 238000005406 washing Methods 0.000 description 3
- OIAQMFOKAXHPNH-UHFFFAOYSA-N 1,2-diphenylbenzene Chemical group C1=CC=CC=C1C1=CC=CC=C1C1=CC=CC=C1 OIAQMFOKAXHPNH-UHFFFAOYSA-N 0.000 description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
- IPBVNPXQWQGGJP-UHFFFAOYSA-N acetic acid phenyl ester Natural products CC(=O)OC1=CC=CC=C1 IPBVNPXQWQGGJP-UHFFFAOYSA-N 0.000 description 2
- 235000015241 bacon Nutrition 0.000 description 2
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 2
- VCCBEIPGXKNHFW-UHFFFAOYSA-N biphenyl-4,4'-diol Chemical compound C1=CC(O)=CC=C1C1=CC=C(O)C=C1 VCCBEIPGXKNHFW-UHFFFAOYSA-N 0.000 description 2
- 230000003670 easy-to-clean Effects 0.000 description 2
- 239000000945 filler Substances 0.000 description 2
- 238000013007 heat curing Methods 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000000178 monomer Substances 0.000 description 2
- 238000000465 moulding Methods 0.000 description 2
- 235000014594 pastries Nutrition 0.000 description 2
- 229940049953 phenylacetate Drugs 0.000 description 2
- WLJVXDMOQOGPHL-UHFFFAOYSA-N phenylacetic acid Chemical compound OC(=O)CC1=CC=CC=C1 WLJVXDMOQOGPHL-UHFFFAOYSA-N 0.000 description 2
- 229920005668 polycarbonate resin Polymers 0.000 description 2
- 239000004431 polycarbonate resin Substances 0.000 description 2
- 239000000376 reactant Substances 0.000 description 2
- 230000002441 reversible effect Effects 0.000 description 2
- 239000002002 slurry Substances 0.000 description 2
- 239000000344 soap Substances 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 230000007704 transition Effects 0.000 description 2
- NNJPGOLRFBJNIW-HNNXBMFYSA-N (-)-demecolcine Chemical compound C1=C(OC)C(=O)C=C2[C@@H](NC)CCC3=CC(OC)=C(OC)C(OC)=C3C2=C1 NNJPGOLRFBJNIW-HNNXBMFYSA-N 0.000 description 1
- XJKSTNDFUHDPQJ-UHFFFAOYSA-N 1,4-diphenylbenzene Chemical group C1=CC=CC=C1C1=CC=C(C=2C=CC=CC=2)C=C1 XJKSTNDFUHDPQJ-UHFFFAOYSA-N 0.000 description 1
- PUOJAJGUVQMPPN-UHFFFAOYSA-N 4-hydroxybenzoic acid;2-phenylacetic acid Chemical compound OC(=O)CC1=CC=CC=C1.OC(=O)C1=CC=C(O)C=C1 PUOJAJGUVQMPPN-UHFFFAOYSA-N 0.000 description 1
- 239000005711 Benzoic acid Substances 0.000 description 1
- 229930185605 Bisphenol Natural products 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- 240000004160 Capsicum annuum Species 0.000 description 1
- 235000002568 Capsicum frutescens Nutrition 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- 239000004642 Polyimide Substances 0.000 description 1
- XSTXAVWGXDQKEL-UHFFFAOYSA-N Trichloroethylene Chemical group ClC=C(Cl)Cl XSTXAVWGXDQKEL-UHFFFAOYSA-N 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 125000003545 alkoxy group Chemical group 0.000 description 1
- 235000010233 benzoic acid Nutrition 0.000 description 1
- 239000004305 biphenyl Substances 0.000 description 1
- 235000010290 biphenyl Nutrition 0.000 description 1
- 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 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 239000007859 condensation product Substances 0.000 description 1
- MGNCLNQXLYJVJD-UHFFFAOYSA-N cyanuric chloride Chemical compound ClC1=NC(Cl)=NC(Cl)=N1 MGNCLNQXLYJVJD-UHFFFAOYSA-N 0.000 description 1
- USIUVYZYUHIAEV-UHFFFAOYSA-N diphenyl ether Chemical compound C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 description 1
- 239000000374 eutectic mixture Substances 0.000 description 1
- 239000003365 glass fiber Substances 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 239000013529 heat transfer fluid Substances 0.000 description 1
- 230000002452 interceptive effect Effects 0.000 description 1
- 239000002655 kraft paper Substances 0.000 description 1
- 235000013372 meat Nutrition 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 229930184652 p-Terphenyl Natural products 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920001225 polyester resin Polymers 0.000 description 1
- 239000004645 polyester resin Substances 0.000 description 1
- 229920001721 polyimide Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920001343 polytetrafluoroethylene Polymers 0.000 description 1
- 239000004810 polytetrafluoroethylene Substances 0.000 description 1
- 239000000779 smoke Substances 0.000 description 1
- 230000000391 smoking effect Effects 0.000 description 1
- 239000011343 solid material Substances 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 150000003457 sulfones Chemical class 0.000 description 1
- LXEJRKJRKIFVNY-UHFFFAOYSA-N terephthaloyl chloride Chemical compound ClC(=O)C1=CC=C(C(Cl)=O)C=C1 LXEJRKJRKIFVNY-UHFFFAOYSA-N 0.000 description 1
- 150000001911 terphenyls Chemical class 0.000 description 1
- 238000005809 transesterification reaction Methods 0.000 description 1
- 230000004580 weight loss Effects 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
- C08G63/02—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds
- C08G63/12—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds derived from polycarboxylic acids and polyhydroxy compounds
- C08G63/16—Dicarboxylic acids and dihydroxy compounds
- C08G63/18—Dicarboxylic acids and dihydroxy compounds the acids or hydroxy compounds containing carbocyclic rings
-
- 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
- C08G63/02—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds
- C08G63/60—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds derived from the reaction of a mixture of hydroxy carboxylic acids, polycarboxylic acids and polyhydroxy compounds
- C08G63/605—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds derived from the reaction of a mixture of hydroxy carboxylic acids, polycarboxylic acids and polyhydroxy compounds the hydroxy and carboxylic groups being bound to aromatic rings
-
- A—HUMAN NECESSITIES
- A47—FURNITURE; DOMESTIC ARTICLES OR APPLIANCES; COFFEE MILLS; SPICE MILLS; SUCTION CLEANERS IN GENERAL
- A47J—KITCHEN EQUIPMENT; COFFEE MILLS; SPICE MILLS; APPARATUS FOR MAKING BEVERAGES
- A47J27/00—Cooking-vessels
- A47J27/06—Steam-heated kettles for domestic use
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Food Science & Technology (AREA)
- Polyesters Or Polycarbonates (AREA)
- Table Devices Or Equipment (AREA)
- Cookers (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US7397879A | 1979-09-10 | 1979-09-10 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH650392A5 true CH650392A5 (de) | 1985-07-31 |
Family
ID=22116966
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH6781/80A CH650392A5 (de) | 1979-09-10 | 1980-09-09 | Feuerfestes geschirr auf basis eines geformten, gegebenenfalls modifizierten homo- oder copolyesters. |
Country Status (30)
| Country | Link |
|---|---|
| JP (1) | JPS5643319A (OSRAM) |
| KR (1) | KR860001372B1 (OSRAM) |
| AU (1) | AU528537B2 (OSRAM) |
| BE (1) | BE884391A (OSRAM) |
| BR (1) | BR8005198A (OSRAM) |
| CA (1) | CA1196146A (OSRAM) |
| CH (1) | CH650392A5 (OSRAM) |
| DE (1) | DE3034041C2 (OSRAM) |
| DK (1) | DK382980A (OSRAM) |
| FI (1) | FI75351C (OSRAM) |
| FR (1) | FR2464683A1 (OSRAM) |
| GB (1) | GB2058102B (OSRAM) |
| GR (1) | GR68477B (OSRAM) |
| HK (1) | HK78384A (OSRAM) |
| IE (1) | IE50008B1 (OSRAM) |
| IT (1) | IT1132717B (OSRAM) |
| KE (1) | KE3431A (OSRAM) |
| LU (1) | LU82666A1 (OSRAM) |
| MA (1) | MA18944A1 (OSRAM) |
| MX (1) | MX160058A (OSRAM) |
| MY (1) | MY8500678A (OSRAM) |
| NL (1) | NL190100C (OSRAM) |
| NO (1) | NO802407L (OSRAM) |
| NZ (1) | NZ194443A (OSRAM) |
| PH (1) | PH19274A (OSRAM) |
| PL (1) | PL226655A1 (OSRAM) |
| PT (1) | PT71783B (OSRAM) |
| SE (1) | SE8006290L (OSRAM) |
| SG (1) | SG44384G (OSRAM) |
| ZA (1) | ZA804425B (OSRAM) |
Families Citing this family (28)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4318841A (en) * | 1980-10-06 | 1982-03-09 | Celanese Corporation | Polyester of 6-hydroxy-2-naphthoic acid, para-hydroxy benzoic acid, terephthalic acid, and resorcinol capable of readily undergoing melt processing to form shaped articles having increased impact strength |
| DE3365769D1 (en) * | 1982-03-08 | 1986-10-09 | Celanese Corp | Preparation of aromatic polyesters by direct polycondensation |
| US4639504A (en) * | 1982-06-08 | 1987-01-27 | Dart Industries Inc. | Production of thermally stabilized aromatic polyesters |
| CA1220889A (en) * | 1982-06-08 | 1987-04-21 | Dart Industries Inc. | Process for the production of aromatic polyesters |
| IE54564B1 (en) * | 1982-07-26 | 1989-11-22 | Dart Ind Inc | Polyester moulding compositions and ovenware therefrom |
| JPS5962630A (ja) * | 1982-07-26 | 1984-04-10 | セラニ−ズ・コ−ポレイシヨン | 比較的低濃度の６−オキシ−２−ナフトイル部分を含む異方性溶融加工可能なポリエステル |
| US4626557A (en) * | 1982-07-26 | 1986-12-02 | Dart Industries, Inc. | Plastic ovenware containing talc |
| US4431770A (en) * | 1982-07-29 | 1984-02-14 | Celanese Corporation | Wholly aromatic polyester comprising 4-oxy-4'-carboxybiphenyl moiety which is capable of forming an anisotropic melt phase |
| JPS5951915A (ja) * | 1982-07-29 | 1984-03-26 | セラニ−ズ・コ−ポレ−シヨン | ６−オキシ−２−ナフトイル成分及び４−オキシ−４′−カルボキシビフエニル成分を含んで成る全芳香族ポリエステル |
| US4399270A (en) * | 1982-07-29 | 1983-08-16 | E. I. Du Pont De Nemours & Co. | Fiber-forming polyesters of ketodiols |
| US4398015A (en) * | 1982-08-03 | 1983-08-09 | E. I. Du Pont De Nemours & Company | Fiber-forming polyesters of aromatic ketohydroxy acids |
| US4447592A (en) * | 1983-06-13 | 1984-05-08 | E. I. Du Pont De Nemours And Company | Anisotropic melt polyesters of 6-hydroxy-2-naphthoic acid |
| DE3325705A1 (de) * | 1983-07-16 | 1985-01-24 | Bayer Ag, 5090 Leverkusen | Mesomorphe aromatische polyester mit hoher zaehigkeitund verbesserter schmelzviskositaet, verfahren zu ihrer herstellung und ihre verwendung zur herstellung von formkoerpern, filamenten, fasern und folien |
| US4694061A (en) * | 1983-10-12 | 1987-09-15 | Ciba-Geigy Corporation | Radiation-sensitive polycondensates, processes for their preparation coated material and its use |
| DE3338805A1 (de) * | 1983-10-26 | 1985-05-15 | Basf Ag, 6700 Ludwigshafen | Vollaromatische polyester |
| JPS60188421A (ja) * | 1984-03-09 | 1985-09-25 | Agency Of Ind Science & Technol | 共重合ポリエステル |
| JPS61316A (ja) * | 1984-06-13 | 1986-01-06 | 住友化学工業株式会社 | オ−ブンウエア |
| DE3427886A1 (de) * | 1984-07-28 | 1986-01-30 | Bayer Ag, 5090 Leverkusen | Thermotrope aromatische polyester mit hoher steifigkeit, verfahren zu ihrer herstellung und ihre verwendung zur herstellung von formkoerpern, filamenten, fasern und folien |
| JPS61199821A (ja) * | 1985-03-01 | 1986-09-04 | 住友化学工業株式会社 | 非粘着性を有するプラスチックオ−ブンウエア |
| DE3534730A1 (de) * | 1985-09-28 | 1987-04-09 | Bayer Ag | Thermotrope vollaromatische polyester mit ausgezeichneter steifigkeit und zaehigkeit, verfahren zu ihrer herstellung und ihre verwendung zur herstellung von formkoerpern, filamenten, fasern und folien |
| JPH07106595B2 (ja) * | 1987-04-24 | 1995-11-15 | 呉羽化学工業株式会社 | 熱成形ポリアリ−レンスルフイド容器及びその製造法 |
| US4851480A (en) * | 1987-06-09 | 1989-07-25 | Amoco Corporation | Extrusion-grade compositions comprising mixtures of wholly aromatic polyesters |
| EP0317616B1 (en) * | 1987-06-09 | 1993-04-14 | Amoco Corporation | Molding compositions comprising mixtures of wholly aromatic polyesters and fillers |
| US4952663A (en) * | 1988-06-17 | 1990-08-28 | Amoco Corporation | Wholly aromatic polyesters with reduced char content |
| US4849499A (en) * | 1988-08-01 | 1989-07-18 | Eastman Kodak Company | Melt processable, liquid crystalline polyesters |
| IT1227902B (it) * | 1988-12-23 | 1991-05-14 | Enichem Spa | Copolimeri termotropici liquido-cristallini aromatici |
| FR2653436A1 (fr) * | 1989-10-24 | 1991-04-26 | Atochem | Copolyesters aromatiques thermotropes et leur procede de preparation. |
| EP0656385A4 (en) * | 1993-06-15 | 1997-10-22 | Nippon Petrochemicals Co Ltd | FULLY AROMATIC POLYESTER, COMPOSITION MADE THEREWITH, AND MOLDED ARTICLE MANUFACTURED THEREFROM. |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3637595A (en) * | 1969-05-28 | 1972-01-25 | Steve G Cottis | P-oxybenzoyl copolyesters |
| BE789542A (fr) * | 1971-10-01 | 1973-03-29 | Carborundum Co | Production d'un polyester de para-oxybenzoyle infusible et faconnable |
| US3884876A (en) * | 1973-08-31 | 1975-05-20 | Carborundum Co | Partially crosslinked linear aromatic polyesters |
| US3980749A (en) * | 1973-08-31 | 1976-09-14 | The Carborundum Company | Partially crosslinked linear aromatic polyesters |
-
1980
- 1980-07-15 IE IE1468/80A patent/IE50008B1/en unknown
- 1980-07-17 FI FI802261A patent/FI75351C/fi not_active IP Right Cessation
- 1980-07-18 BE BE0/201464A patent/BE884391A/fr not_active IP Right Cessation
- 1980-07-21 GR GR62517A patent/GR68477B/el unknown
- 1980-07-22 ZA ZA00804425A patent/ZA804425B/xx unknown
- 1980-07-22 AU AU60688/80A patent/AU528537B2/en not_active Ceased
- 1980-07-25 NZ NZ194443A patent/NZ194443A/xx unknown
- 1980-07-29 MX MX183340A patent/MX160058A/es unknown
- 1980-07-29 LU LU82666A patent/LU82666A1/fr unknown
- 1980-07-29 PH PH24363A patent/PH19274A/en unknown
- 1980-08-06 CA CA000357731A patent/CA1196146A/en not_active Expired
- 1980-08-08 FR FR8017614A patent/FR2464683A1/fr active Granted
- 1980-08-12 NO NO802407A patent/NO802407L/no unknown
- 1980-08-18 BR BR8005198A patent/BR8005198A/pt unknown
- 1980-08-26 JP JP11763480A patent/JPS5643319A/ja active Granted
- 1980-08-28 NL NLAANVRAGE8004863,A patent/NL190100C/xx not_active IP Right Cessation
- 1980-09-04 MA MA19145A patent/MA18944A1/fr unknown
- 1980-09-05 KR KR1019800003507A patent/KR860001372B1/ko not_active Expired
- 1980-09-09 GB GB8029092A patent/GB2058102B/en not_active Expired
- 1980-09-09 DK DK382980A patent/DK382980A/da not_active Application Discontinuation
- 1980-09-09 PT PT71783A patent/PT71783B/pt unknown
- 1980-09-09 PL PL22665580A patent/PL226655A1/xx unknown
- 1980-09-09 SE SE8006290A patent/SE8006290L/ unknown
- 1980-09-09 IT IT24554/80A patent/IT1132717B/it active
- 1980-09-09 CH CH6781/80A patent/CH650392A5/de not_active IP Right Cessation
- 1980-09-10 DE DE3034041A patent/DE3034041C2/de not_active Expired
-
1984
- 1984-06-19 SG SG44384A patent/SG44384G/en unknown
- 1984-07-20 KE KE3431A patent/KE3431A/xx unknown
- 1984-10-18 HK HK783/84A patent/HK78384A/xx not_active IP Right Cessation
-
1985
- 1985-12-30 MY MY678/85A patent/MY8500678A/xx unknown
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PUE | Assignment |
Owner name: AMOCO CORPORATION |
|
| PL | Patent ceased |