Inventor
CALUNDANN GORDON W
US49 patents
⚠️ This page may combine multiple inventors who share the name “CALUNDANN GORDON W”. Patents are grouped by organization below to help distinguish them — per-person disambiguation is on the roadmap.
CELANESE CORP
33 patentsUS4161470AJul 17, 1979
Polyester of 6-hydroxy-2-naphthoic acid and para-hydroxy benzoic acid capable of readily undergoing melt processing
CELANESE CORP405 citations99
US4067852AJan 10, 1978
Melt processable thermotropic wholly aromatic polyester containing polybenzoyl units
CELANESE CORP187 citations99
US4219461AAug 26, 1980
Polyester of 6-hydroxy-2-naphthoic acid, para-hydroxy benzoic acid, aromatic diol, and aromatic diacid capable of readily undergoing melt processing
CELANESE CORP149 citations97
US4130545ADec 19, 1978
Melt processable thermotropic wholly aromatic polyester comprising both para-oxybenzoyl and meta-oxybenzoyl moieties
CELANESE CORP153 citations97
US4522974AJun 11, 1985
Melt processable polyester capable of forming an anisotropic melt comprising a relatively low concentration of 6-oxy-2-naphthoyl moiety-4-benzoyl moiety, 1,4-dioxyphenylene moiety, isophthaloyl moiety and terephthaloyl moiety
CELANESE CORP110 citations96
US4473682ASep 25, 1984
Melt processable polyester capable of forming an anisotropic melt comprising a relatively low concentration of 6-oxy-2-naphthoyl moiety, 4-oxybenzoyl moiety, 4,4'-dioxybiphenyl moiety, and terephthaloyl moiety
CELANESE CORP115 citations96
US4434262AFeb 28, 1984
Melt processable blend of a low molecular weight liquid crystalline compound and a polyolefin or polyester
CELANESE CORP58 citations96
US4355132AOct 19, 1982
Anisotropic melt phase forming poly(ester-amide) derived from p-hydroxybenzoic acid, 2,6-naphthalenedicarboxylic acid, aromatic monomer capable of forming an amide linkage, and, optionally, hydroquinone and additional carbocyclic dicarboxylic acid
CELANESE CORP101 citations96
US4355134AOct 19, 1982
Wholly aromatic polyester capable of forming an anisotropic melt phase at an advantageously reduced temperature
CELANESE CORP58 citations96
US4351918ASep 28, 1982
Poly(ester-amide) capable of forming an anisotropic melt phase derived from 6-hydroxy-2-naphthoic acid, other aromatic hydroxyacid, carbocyclic dicarboxylic acid, and aromatic monomer capable of forming an amide linkage
CELANESE CORP96 citations96
US4351917ASep 28, 1982
Poly(ester-amide) capable of forming an anisotropic melt phase derived from 6-hydroxy-2-naphthoic acid, aromatic monomer capable of forming an amide linkage, and other aromatic hydroxyacid
CELANESE CORP95 citations96
US4339375AJul 13, 1982
Poly(ester-amide) capable of forming an anisotropic melt phase derived from p-hydroxybenzoic acid, 2,6-dihydroxynaphthalene, carbocyclic dicarboxylic acid, aromatic monomer capable of forming an amide linkage, and, optionally, additional aromatic diol
CELANESE CORP64 citations96
US4337190AJun 29, 1982
Polyester of 6-hydroxy-2-naphthoic acid and meta-hydroxy benzoic acid capable of readily undergoing melt processing
CELANESE CORP67 citations96
US4330457AMay 18, 1982
Poly(ester-amide) capable of forming an anisotropic melt phase derived from 6-hydroxy-2-naphthoic acid, dicarboxylic acid, and aromatic monomer capable of forming an amide linkage
CELANESE CORP99 citations96
US4318841AMar 9, 1982
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
CELANESE CORP84 citations96
US4318842AMar 9, 1982
Polyester of 6-hydroxy-2-naphthoic acid, aromatic diol, and 1,4-cyclohexanedicarboxylic acid capable of undergoing melt processing
CELANESE CORP106 citations96
US4279803AJul 21, 1981
Polyester of phenyl-4-hydroxybenzoic acid and 4-hydroxybenzoic acid and/or 6-hydroxy-2-naphthoic acid capable of forming an anisotropic melt
CELANESE CORP64 citations96
US4256624AMar 17, 1981
Polyester of 6-hydroxy-2-naphthoic acid, aromatic diol, and aromatic diacid capable of undergoing melt processing
CELANESE CORP131 citations96
US4184996AJan 22, 1980
Melt processable thermotropic wholly aromatic polyester
CELANESE CORP131 citations96
US4083829AApr 11, 1978
Melt processable thermotropic wholly aromatic polyester
CELANESE CORP254 citations96
US4375530AMar 1, 1983
Polyester of 2,6-naphthalene dicarboxylic acid, 2,6-dihydroxy naphthalene, terephthalic acid, and hydroquinone capable of forming an anisotropic melt
CELANESE CORP87 citations93
US4654412AMar 31, 1987
Linear, melt processable, crosslinkable, thermotropic wholly aromatic polyesters and crosslinked polymers prepared therefrom
CELANESE CORP28 citations92
US4355133AOct 19, 1982
Polyester of 6-hydroxy-2-naphthoic acid, 4-hydroxy benzoic acid, 1,4-cyclohexanedicarboxylic acid, and aromatic diol capable of readily undergoing melt processing to form articles possessing high impact properties
CELANESE CORP22 citations82
US4299756ANov 10, 1981
Polyester of phenyl-4-hydroxybenzoic acid, aromatic diol, and aromatic diacid capable of forming an anisotropic melt
CELANESE CORP20 citations82
US4224433ASep 23, 1980
Thermotropic polyesters of 2,6-dihydroxyanthraquinone
CELANESE CORP19 citations82
US4431770AFeb 14, 1984
Wholly aromatic polyester comprising 4-oxy-4'-carboxybiphenyl moiety which is capable of forming an anisotropic melt phase
CELANESE CORP12 citations74
US4395513AJul 26, 1983
High performance thermally stable poly(6-oxy-2-naphthoate)
CELANESE CORP13 citations74
US4371660AFeb 1, 1983
Anisotropic melt phase forming poly(ester-carbonate) derived from 6-hydroxy-2-napthoic acid, aromatic diol, organic compound capable of forming a carbonate linkage, and, optionally, other aromatic hydroxy-acid and carbocyclic dicarboxylic acid
CELANESE CORP14 citations74
US4048139ASep 13, 1977
Rendering polybenzimidazole solid materials more resistant to darkening upon exposure to light
CELANESE CORP13 citations74
US4321182AMar 23, 1982
Stable non-corrosive solution of polybenzimidazole suitable for use in the formation of shaped articles
CELANESE CORP7 citations68
US4429100AJan 31, 1984
Polyester of 6-hydroxy-2-naphthoic acid, para-hydroxybenzoic acid, 2,6-dioxyanthraquinone, and aromatic diacid
CELANESE CORP6 citations63
US4341688AJul 27, 1982
Poly(ester-amide) capable of forming an anisotropic melt phase derived from dihydroxyanthraquinone, hydroxybenzoic acid, dicarboxylic acid, and aromatic monomer capable of forming an amide linkage
CELANESE CORP5 citations63
US4245084AJan 13, 1981
Thermotropic, wholly aromatic polythiolesters capable of forming an anisotropic melt and a process for preparing the polythiolesters
CELANESE CORP3 citations63
HOECHST CELANESE CORP
15 patentsUS4868274ASep 19, 1989
Polyanhydride from carboxy aryloxy alkanoic acid
HOECHST CELANESE CORP59 citations96
US5171823ADec 15, 1992
Melt processable thermotropic wholly aromatic polyester containing 6-hydroxy-2-naphthoic acid moieties
HOECHST CELANESE CORP22 citations93
US5091087AFeb 25, 1992
Fabrication of microporous PBI membranes with narrow pore size distribution
HOECHST CELANESE CORP26 citations93
US4746694AMay 24, 1988
Melt processable polyester capable of forming an anisotropic melt comprising a relatively low concentration of 6-oxy-2-naphthoyl moiety, 4-oxybenzoyl moiety, 2,6-dioxynaphthalene moiety, and terephthaloyl moiety
HOECHST CELANESE CORP37 citations93
US5250633AOct 5, 1993
Fibers and fibrets from blends of polybezimidazoles and aromatic polyamides, aromatic polyamide-hydrazides or aromatic polyamides containing heterocyclic linkages
HOECHST CELANESE CORP26 citations92
US5164478ANov 17, 1992
Process for producing polyarylate having low color
HOECHST CELANESE CORP43 citations92
US5290884AMar 1, 1994
Blends of polybenzimidazoles and aromatic polyamides, aromatic polyamide-hydrazides or aromatic polyamides containing heterocyclic linkages
HOECHST CELANESE CORP19 citations81
US5140093AAug 18, 1992
Melt-processable thermotropic polyesters having fluorine containing linking groups
HOECHST CELANESE CORP8 citations74
US4922003AMay 1, 1990
Bisacrylate monomers and polymers exhibiting nonlinear optical response
HOECHST CELANESE CORP9 citations74
US4997603AMar 5, 1991
Process for formation of halogenated polymeric microporous membranes having improved strength properties
HOECHST CELANESE CORP16 citations73
US4957655ASep 18, 1990
Copolymeric nonlinear optical media
HOECHST CELANESE CORP17 citations73
US4910106AMar 20, 1990
Formation of halogenated polymeric microporous membranes having improved strength properties
HOECHST CELANESE CORP10 citations73
US5023314AJun 11, 1991
Novel polyarylate compositions having improved properties
HOECHST CELANESE CORP4 citations63
US4963633AOct 16, 1990
Bisacrylate monomers and polymers exhibiting nonlinear optical response
HOECHST CELANESE CORP2 citations63
US4929696AMay 29, 1990
Bisacrylate monomers and polymers exhibiting nonlinear optical response
HOECHST CELANESE CORP3 citations63