Eastman-kodak Company

Eastman Chemical Company

Cornell Development Corporation LLC

Cornell Development Group, LLC

David Dunlap Cornell

Carl M Lentz

James R Overton

Michael Paul Ekart

Thomas Michael Pell, Jr

Michael R Cushman

Damon Bryan Shackelford

Leonard H Wojcik, Jr

Timothy Edward Long

Stephen W Cornell

Donald Lee Carver

Paul W Cornell

Damon Brian Shackelford

Disclosed are diaryl iodonium compositions with antimicrobial activity and low toxicity to plants and mammals. The present diaryl iodonium compositions include a tri-substituted aryl group and a heteroaryl group which produce substantially no chlorobenzene and/or 1,2-dichlorobenzene when applied to microbes.

Antimicrobial diaryl iodonium compositions and method

The present invention provides an electrochemical method for producing diaryl iodonium compounds wherein application of an electric current to an electrochemical cell containing a reaction mixture composed of a solvent, an iodoaryl compound and an electrolyte forms an oxidizing agent in situ. In this first step, the oxidizing agent is subsequently converted into a stable oxidized iodoaryl intermediate, typically an iodosyl compound. The electric potential is removed and in a second step a target aryl compound is introduced to the reaction mixture to react with the oxidized iodoaryl intermediate to form a diaryl iodonium compound.

Process for the production of diaryl iodonium compounds

The present invention provides a composition having biological activity. The composition includes from about 10 ppm to about 5000 parts iodonium salt. The composition also includes from about 100 ppm to about 300,000 ppm of a compound to act as a carrier of the iodonium compound. The carrier is selected from at least one of polyvinyl alcohols, polyvinyl acetates, polyethylene glycols, ethylene glycol and propylene glycol block copolymers, cellulosic polymers, polyesters, alkyd polymers. The composition also includes from about 50 ppm to about 50,000 ppm of a compound to render the composition compatible with a surface being treated. This component is selected from at least one of di-acids, acid anhydrides, polyfunctional acids, di-ethylene glycol, resorcinol and the like. The composition also includes an appropriate vehicle selected from at least one of water, acidified water, paint, primer, and petroleum distillates. The invention also includes numerous methods of using the above composition by applying the composition to a surface to be treated.

Compositions of iodonium compounds and methods and uses thereof

A process for producing high quality TPA suitable for PET feedstock material from recycled polyester. The process includes the steps of depolymerizing the polyester to form DMT; separating the DMT from secondary materials; and hydrolyzing the DMT to form TPA. In a preferred embodiment of the invention the recycled polyester is contacted with a component monomer or oligomer thereof to liquefy the polyester prior to depolymerizing the polyester.

Process for recycling polyesters

An apparatus for depolymerizing recycled polyester into its component ester monomers and half esters includes a first reactor for depolymerizing the recycled polyester, a separator for separating ester monomeric components and half-esters from secondary materials produced in the first reactor, and a second reactor for producing a low molecular weight polyester from liquefied separator products.

Depolymerization apparatus for recycling polyesters

A process for recovering suitable polyester feedstock material from recycled polyester includes the steps of depolymerizing the polyester into its component ester monomers and half-esters; separating the monomers and half-esters from other secondary materials; and mixing the component ester monomers and half-esters with additional monomers to produce a low molecular weight polyester. In a preferred embodiment of the invention the recycled polyester is contacted with a component monomer or oligomer thereof to liquefy the polyester before the polyester is depolymerized. The invention further provides an apparatus for carrying out the process. The apparatus includes a first reactor for depolymerizing the recycled polyester, a separator for separating ester monomeric components and half-esters from secondary materials produced in the first reactor, and a second reactor for producing a low molecular weight polyester from the liquefied separator products.

Depolymerization process for recycling polyesters

A polyester having increased UV absorption comprising (i) a residue of a dicarboxylic acid component comprising terephthalic and from about 1 to about 20 mole % of isophthalic acid, (ii) a residue of a glycol component comprising ethylene glycol, and (iii) from about 0.01 mole % to about 15 mole % of a residue of an aromatic diol derivative, wherein the aromatic diol derivative has a least two polyester reactive groups that are capable of participating in a polyester-forming reaction and the total mole % for components (i), (ii) and (iii) is 200 mole %.

Polyester comprising a residue of isophthalic acid, terephthalic acid,

Electrochemical process for preparing diaryliodonium salts using a single compartment and a carbon anode. The process has high current efficiency and, optionally, increased para, para' regioselectivity. The process proceeds in the presence of a solvent such as acetic acid and an electrolyte such as a compound of fluorine or sulfuric acid.

Electrochemical synthesis of diaryliodonium salts

An electrolytic method for the simultaneous preparation of a diaryliodonium salt and an alkoxide salt comprises adding to the anode compartment of an electrolytic cell, comprised of an anode, a first electrolytic solution comprising an aromatic compound, an iodoaromatic compound, a solvent and a first organic salt; adding to the cathode compartment of the cell, comprised of a cathode, a second electrolytic solution comprising a hydroxyalkyl compound and a second organic salt; and applying to the anode and the cathode an electric potential, to form diaryliodonium salt in the anode compartment and an alkoxide salt in the cathode compartment. Esters of an aromatic acid are prepared by carbonylating an admixture of the diaryliodonium salt and the alkoxide salt by the addition of carbon monoxide thereto.

Electrolytic method of simultaneously preparing diaryliodonium salt and

The present invention provides a process for the preparation of aromatic dicarboxylic acids by the carbonylation of aromatic diiodides. The aromatic diiodides are reacted with carbon monoxide in the presence of a soluble rhodium catalyst in a hydrocarbon acid reaction medium to prepare the aromatic dicarboxylic acids.

Carbonylation process for the production of aromatic dicarboxylic acids

The present invention provides a novel process for the preparation of styrene, stilbene, and/or substituted derivatives thereof. The process involves the reaction of an aryl sulfonyl chloride with an olefinic compound in the presence of a catalytic amount of a metal catalyst consisting essentially of palladium.

Preparation of styrene and stilbene compounds

The present invention provides a process for the preparation of aryl carboxylic acids and derivatives thereof by the carbonylation of diaryliodonium salts. The diaryliodonium salts are reacted with carbon monoxide and water or an alcohol or amine in a base reaction medium having a pK.sub.b greater than about 8.

Carbonylation process for the production of aromatic acids and

The present invention provides a process for the preparation of monoesters of dicarboxylic acids by the carbonylation of carboxyphenyl-triarylphosphonium salts. The carboxyphenyl-triarylphosphonium salts are reacted with carbon monoxide and an alcohol in a base reaction medium having a pK.sub.b greater than about 8.

Carbonylation process for the production of monoesters aromatic

The present invention provides a process for the preparation of aryl carboxylic acids by the carbonylation of diaryliodonium salts. The diaryliodonium salts are reacted with carbon monoxide in the presence of a zero-valent palladium in a hydrocarbon acid reaction medium to prepare the aromatic carboxylic acids.

Carbonylation process for the production of aromatic acids

The present invention provides a process for the preparation of aryl carboxylic acids and derivatives thereof by the carbonylation of aryl sulfonyl chlorides. The aryl sulfonyl chlorides are reacted with carbon monoxide and water or an alcohol or amine in the presence of a zero-valent metal catalyst consisting essentially of palladium.

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Kingsport, TN, United States of America

David Dunlap Cornell