P

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 patents
US4161470AJul 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 patents
US4868274ASep 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

HOECHST CELANSE CORP

1 patent