Eastman Chemical Company

Other

Eastman-kodak Company

Mote Marine Laboratory

Michael R Cushman

Max Allen Weaver

James J Krutak

William W Parham

Gabor Patonay

Avron I Bryan

Joseph Robert Zoeller

Clarence A Coates, Jr

Brent Alan Tennant

Clarence A Coates

Nick Allen Collins

David Dunlap Cornell

Steven Thomas Perri

Carl M Lentz

Bhaskar Krishna Arumugam

Regina M Moncier

Vincent Alvin Nicely

James R Overton

Chester Wayne Sink

Brendan William Boyd

Joseph Nathaniel Bays

Jeffery Earl Grant Powell

Richard H Pierce, Jr

Transito Lynne Macias

Jeffrey Earl Grant Powell

The present invention describes a method for controlling growth of harmful algal blooms generated by the red tide organism,, and other harmful algal species. The method includes the steps of applying seawater containing low levels of dissolved ozone directly onto or under the surface of water containing harmful algal blooms. Since only low levels of ozone are required for this method to be effective and since the application of ozonated seawater is directed to the bloom itself, release of excess ozone into the atmosphere and/or surrounding water is minimal, which is advantageous since it greatly reduces adverse effects of ozone on the environment, marine life, and human health. The low concentration of ozone utilized in this method is sufficient to destroy the red tide organism, but leave surrounding marine life unharmed.

Use of ozone for controlling growth of organisms

The present invention comprises the use of sulfite additives to reduce discoloration of L-ascorbic acid produced from acid or aqueous solutions of 2-keto-L-gulonic acid. In one aspect, the present invention comprises a continuous process for producing L-ascorbic acid from an aqueous solution of 2-keto-L-gulonic acid. The use of sulfite additives reduces product stream color and improves product recovery by binding to high molecular weight reaction by-products. In a continuous process, the reaction stream is separated from residual sulfite and sulfite-bound by-products to produce a product stream enriched in aqueous ascorbic acid for recovery, and an enriched 2-keto-L-gulonic acid stream which is recycled to the reactor. The in situ use of sulfite additives during the reaction increases the overall yield of L-ascorbic acid, with no loss in selectivity of the synthesis.

Process for producing ascorbic acid

The present invention provides methods and an apparatus for the manufacture of an L-ascorbic acid product in high yield by direct conversion of an aqueous solution containing 2-keto-L-gulonic acid by contact with an acid catalyst or under thermal self-catalyzed conditions at a conversion level that maximizes the formation of L-ascorbic acid and minimizes decomposition of the L-ascorbic acid thus formed. The separation process for L-ascorbic acid and KLG is operated in such a way that an efficient separation process allows the majority of the KLG to be recycled for further conversion. The product stream from the separation process is then subjected to a recovery step to obtain crystalline L-ascorbic acid product.

Continuous process for producing L-ascorbic acid

In a liquid phase carbonylation process for the production of acetic anhydride by reacting a feed stream which includes methyl acetate, methanol and carbon monoxide using a Group VIII metal-containing catalyst, and preferably a rhodium containing material, a liquid reaction product is continuously withdrawn from the carbonylation zone and fed to an evaporation/separation zone for separating volatile constituents of the reaction from the non-volatile constituents which, includes a portion of the Group VIII metal catalyst from the carbonylation reactor. The Group VIII metal catalyst is contacted with a gas stream which includes hydrogen for a period of from about 0.001 seconds to about 200 seconds as it is being returned to the carbonylation zone.

Method for reducing EDA in acetic anhydride production

Provided are new compounds useful as near infrared fluorophoric markers. In the practice of this invention a method is also provided for tagging thermoplastic containers using near infrared fluorescing compounds or copolymerized residues readily capable of detection. The new compounds are phthalocyanine and naphthalocyanine derivatives which are covalently bonded to substituted silicon and aluminum compounds. The methods, compositions, and compounds described herein thus provide a total system useful for marking, for identification purposes, the various classes of thermoplastic wastes, so that they can be identified, sorted, and subsequently recycled.

Method for tagging thermoplastic materials with near infrared

Provided is a method for tagging thermoplastic containers using near infrared fluorescing compounds or copolymerized residues readily capable of detection. Also provided is a method for identifying a thermoplastic container. Also provided are thermoplastic polymer compositions comprised of the near infrared fluorescing compounds or residues and articles comprised of such compositions.

Method for detecting and separating thermoplastic containers with near

This invention provides a method for imparting invisible markings for identification purposes to petroleum hydrocarbons by incorporating one or more infrared fluorescing compounds therein. Certain infrared fluorophores from the classes of squaraines (derived from squaric acid), phthalocyanines and naphthalocyanines are useful in providing invisibly marked petroleum hydrocarbons such as crude oil, lubricating oils, waxes, gas oil (furnace oil), diesel oil, kerosene and in particular gasoline. The near infrared fluorophores are added to the hydrocarbons at extremely low levels and are detected by exposing the marked hydrocarbon compositions to near infrared radiation having a wavelength in the 670-850 nm range and then detecting the emitted fluorescent light via near infrared light detection means.

Method for tagging petroleum products

Provided is a method for tagging thermoplastic containers using near infrared fluorescing compounds or copolymerized residues readily capable of detection. Also provided is a method for identifying a thermoplastic container. Also provided are thermoplastic polymer compositions comprised of the near infrared fluorescing compounds or residues and articles comprised of such compositions. Also provided are new compounds useful as near infrared fluorophoric markers in the practice of this invention. The methods, compositions, and compounds of the present invention thus provide a total system useful for marking, for identification purposes, the various classes of thermoplastic wastes, so that they can be identified, sorted, and subsequently recycled.

Provided are water-dissipatable, sulfo-containing polyesters and polyester-amides having copolymerized therein thermally stable near infrared flourophoric compounds. The polymers are useful in coating or ink compositions, which are in turn useful for marking articles for identification/authentication purposes. Also provided is a method for invisibly marking such articles and a method for detecting and sorting articles by utilizing the near infrared flourophoric ink or coating compositions.

Water-dissipatable polyesters and amides containing near infrared

Thermoplastic materials containing near infrared fluorophores

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

A device for in situ cleaning a fouled membrane of a sensor disposed in an aqueous process solution includes a first electrolysis electrode disposed in the process solution immediately adjacent the membrane, a second electrolysis electrode disposed in the process solution and spaced apart from the first electrolysis electrode, and a controllable power source for passing a current between said first and second electrodes. The current produces a heavy concentration of ions at a surface of the fouled membrane. The polarity of the current is selectable to produce negative or positive ions for reacting to decompose deposited salts, or to scrub contaminates from the membrane surface.

Device for in situ cleaning a fouled sensor membrane of deposits

Disclosed is a process for the coproduction of (1) an alkyl iodide and (2) an .alpha.-iodocarboxylic acid, a mono-.alpha.-iodocarboxylic anhydride or a mixture thereof which comprises contacting a mixture of an iodine compound and a carboxylic anhydride with a peroxide at an elevated temperature.

Growing community of inventors

Kingsport, TN, United States of America

Michael R Cushman