Eastman-kodak Company

Exxon Research and Engineering Company

Eastman Chemical Company

Xerox Corporation

Eastman Chemical Corporation

S Richard Turner

Richard W Blevins

Robert D Lundberg

Robert James Perry

Thad O Walker

Dennis G Peiffer

Jan Bock

Donald B Siano

John F Yanus

Warren A Thaler

Brigitte I Voit

Bobby J Sublett

Damodar M Pai

Dale S Renfer

Gary Wayne Connell

Pawan K Agarwal

Ralph Martin Kowalik

Christine J Landry

Morris L Evans

Neil T Ferrar

Ralph B Nielsen

David R Fagerburg

David M Teegarden

Milan Stolka

Bradley K Coltrain

Perry Robert J

Robert R Perry

Bradley K Coltran

Dennis G Pfeiffer

Amorphous copolyesters containing residues derived from 2,2&prime;-&lsqb;2,2-&rsqb;(sulfonylbis(4,1-phenyleneoxy))bis(ethanol). They exhibit enhanced heat distortion temperatures and glass transition temperatures without a significant increase in viscosity at low shear rates. The amorphous copolyesters also have improved resistance to attack by lipid solutions and are readily molded and extruded to form medial devices such as connectors, tubes, etc. which are useful for transport of lipids and other medical solutions.

Low melt viscosity amorphous copolyesters having improved resistance to lipids

An amorphous copolyester having a maximum melt viscosity at 1 radian/second and at about 260 to about 290&deg; C. of about 12000 poise, a glass transition temperature ranging from about 88&deg; C. to about 120&deg; C., and an inherent viscosity of at least about 0.6 dl/g. The amorphous copolyesters comprise the reaction product of a diol component and a dicarboxylic acid component. The diol component comprises residues of from about 5.0 to about 50 mole % of 2,2&prime;-(sulfonylbis (4,1-phenyleneoxy))-bis(ethanol) which has the following chemical formula:

Low melt viscosity amorphous copolyesters with enhanced glass transition temperatures having improved gas barrier properties

The invention relates to an amorphous copolyester having a maximum melt viscosity at 1 radian/second and at about 260 to about 290.degree. C. of about 12000 poise, a glass transition temperature ranging from about 88.degree. C. to about 120.degree. C., and an inherent viscosity of at least about 0.6 dl/g. The amorphous copolyesters comprise the reaction product of a diol component and a dicarboxylic acid component. The diol component comprises residues of from about 5.0 to about 50 mole % of 2,2'-(sulfonylbis(4,1 -phenyleneoxy))-bis(ethanol) which has the following chemical formula: ##STR1## and from about 50 to about 95 mole % of a mixture of at least two diols selected from the group consisting of ethylene glycol, neopentyl glycol, 1,3-propanediol, 1,4-butanediol, 1,4-cyclohexanedimethanol, and mixture thereof. The dicarboxylic acid component comprises residues of terephthalic acid, isophthalic acid, 1,4-cyclohexandedicarboxylic acid, 2,6-naphthalene dicarboxylic acid and mixtures thereof. The amorphous copolyesters according to the invention have relatively low melt viscosities and relatively high glass transition temperatures. Because of the low melt viscosities and high glass transition temperatures, copolyesters with increased IV or molecular weight can easily be obtained. The copolyesters according to the invention can be used for molded or extruded articles, sheets, and films. Accordingly, the invention also relates to molded and extruded articles, sheets, and films made from a copolyester as described above.

Low melt viscosity amorphous copolyesters with enhanced glass transition

Copolymers are produced when a 4-vinyl-1,3 dioxolane monomer is copolymerized with an imidized maleic anhydride (for example, maleimide) monomer in the presence of a free radical initiator. Alternatively, a maleamic acid or maleimide functionality may be introduced into a copolymer containing a 4-vinyl-1,3 dioxolane and maleic anhydride by introducing a primary amine into the reaction mixture. Also, the dioxolane reactant may be introduced into the polymer by reacting 3,4-epoxy-1-butene in a ketone reaction solvent. The structure and composition of the product copolymer are controlled by both the sequence and conditions of the reaction. Products of the present invention can be cast as clear films and can also be used as reactive polymers.

Copolymers of vinyl dioxolanes and imidized derivatives of maleic

Copolymers are produced when a 4-vinyl-1,3-dioxolane monomer is copolymerized with an imidized maleic anhydride (for example, maleimide) monomer in the presence of a free radical initiator. Alternatively, a maleamic acid or maleimide functionality may be introduced into a copolymer containing a 4-vinyl-1,3-dioxolane and maleic anhydride by introducing a primary amine into the reaction mixture. Also, the dioxolane reactant may be introduced into the polymer by reacting 3,4-epoxy-1-butene in a ketone reaction solvent. The structure and composition of the product copolymer are controlled by both the sequence and conditions of the reaction. Products of this invention can be cast as clear films and can also be used as reactive polymers.

Copolymers of vinyl dioxolanes and maleimides

Copolymers are produced when a 3,4-epoxy-1-butene monomer is copolymerized with a maleimide monomer in the presence of a free radical initiator. The copolymerization involves both 1,2-propagation and 1,4-propagation of 3,4-epoxy-1-butene. Products of this invention can be cast as clear films and can also be used as reactive polymers.

Copolymers of epoxybutadiene and maleimides

Copolymers are produced when a 4-vinyl-1,3 dioxolane monomer is copolymerized with an imidized maleic anhydride (for example, maleimide) monomer in the presence of a free radical initiator. Alternatively, a maleamic acid or maleimide functionally may be introduced into a copolymer containing a 4-vinyl-1,3 dioxolane and maleic anhydride by introducing a primary amine into the reaction mixture. Also, the dioxolane reactant may be introduced into the polymer by reacting 3,4-epoxy-1-butene in a ketone reaction solvent. The structure and composition of the product copolymer are controlled by both the sequence and conditions of the reaction. Products of the present invention can be cast as clear films and can also be used as reactive polymers.

There is disclosed a composite of 1) a polymer containing repeating units derived from a vinyl carboxylic ester having at least one organo terminated poly(alkylene oxide) side chain with the proviso that the poly(alkylene oxide) is present in an amount greater than 35 mole percent of the total of all backbone monomer units and alkylene oxide units in the polymer and 2) a metal oxide wherein the metal oxide comprises between about 1 and about 60 percent by weight of the composite. The composites can be made by a process comprising the steps of:

Poly(alkylene oxide) vinyl carboxylic ester containing polymer/inorganic

A method for preparing a polymer including the step of reacting carbon monoxide and a reactant pair having respective general formulas ##STR1## and or a reactant having the general formula ##STR2## in the presence of catalyst and free iodo or bromo ions. X is a nonortho halide selected from --Br and --I. n is an integer from 0 to 4. R.sup.1 is selected from the group consisting of alkyl, arylalkyl, aryl, heteroaryl, and cycloalkyl. R.sup.2 is selected from the group consisting of ##STR3## and Each R.sup.5 is independently selected from the group consisting of alkyl and aryl, m is an integer from 1-12, and j is an integer between 0 and 300. R.sup.3 is selected from the group consisting of substituted aryl, unsubstituted aryl, substituted heteroaryl, and unsubstituted heteroaryl.

Method for preparing polyamide-imides from (O, imide and polyamine

A method for preparing a polymer including the step of reacting carbon monoxide and a reactant pair having respective general formulas ##STR1## a reactant having the general formula ##STR2## in the presence of catalyst and free iodo or bromo ions. X is --Br or --I. n is an integer from 0 to 4. R.sup.1 is selected from the group consisting of alkyl, arylalkyl, aryl, heteroaryl, and cycloalkyl. R.sup.2 is selected from the group consisting of ##STR3## wherein each R.sup.5 is independently selected from the group consisting of alkyl and aryl, m is an integer from 1-12, and j is an integer between 0 and 300.

Method for producing polyamide-imides from CO, bis-imide and polyamine

A process for the preparation of aromatic imide sulfide polymers and polymers produced. In the process, elemental sulfur is reacted with a compound having the general formula ##STR1## wherein Z.sup.1 is a direct link and Z.sup.2 is H, or Z.sup.1 has the general structure ##STR2## or Z.sup.1 and Z.sup.2 together complete a moiety having the general structure ##STR3## n= 0-4 . R.sup.1 is substituted or unsubstituted: aryl or heteroaryl. ##STR4## which R.sup.3 is an independently selected aryl group, m is an integer from 1 to 12, and j is an integer from 0 to 300.

Method for the preparation of aromatic imide sulfide polymers

A multiply-branched aliphatic-aromatic polyester and a method for producing that polymer. The method comprises condensing a branching reactant represented by the general formula ##STR1## Each j is 1 or 2, each Ar is independently selected from the group consisting of aromatic and heteroaromatic moieties having a total of ring carbons and heteroatoms of from 5 to about 20, each R.sup.1 is a linking group independently selected from alkyl having from 1 to about 6 carbons, fluoroalkyl having from 1 to about 6 carbons, --O--, --S--, --C.tbd.C--, and ##STR2## Z.sup.1 is selected from the group consisting of hydroxyl and --OSi(CH.sub.3).sub.3, and each Z.sup.2 is independently selected from groups having the structural formula ##STR3## wherein each R.sup.2 is independently selected from the group consisting of hydroxy, chloro, bromo, monovalent alkoxide having from 1 to about 6 carbons, and --O--(CH.sub.2).sub.g --OH, wherein g is an integer from 1 to 3, or Z.sup.1 has the structural formula ##STR4## wherein each R.sup.2 is independently selected from the group consisting of hydroxy, chloro, bromo, monovalent alkoxide having from 1 to about 6 carbons, and --O--(CH.sub.2).sub.g --OH, wherein g is an integer from 1 to 3, and each Z.sup.2 is hydroxyl.

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Pittsford, NY, United States of America

S Richard Turner