Eastman Chemical Company

Union Carbide Chemicals & Plastics Technology Corporation

Renewable Algal Energy, LLC

Dow Global Technolgoies LLC

Other

Dow Technology Investments LLC

Jeffrey Scott Kanel

David Robert Bryant

John N Argyropoulos

Stephen Neal Falling

Brian Michael Roesch

Donald Lee Morrison

Scott Donald Barnicki

Ailene Gardner Phillips

Michael Leo Tulchinsky

Paul Foley

John Robert Briggs

John Michael Maher

David James Miller

Scott Arthur Guelcher

Robert L Clayton

Max Min Lee

Kenneth Wayne Hampton, Jr

Stanley John Okrasinski

David A Babb

Peter Borden Mackenzie

Charles Edwan Sumner, Jr

Zenon Lysenko

Aaron W Sanders

Alan K Schrock

Donald L Bunning

Peter B MacKenzie

Pulikkottil Jacob Thomas

Robert Sterling Kline

Rodger T Marentis

Wei-Jun Peng

Joe D Phillips

Christopher W Derstine

Kurt D Olson

John David Moncier

Mary Kathleen Foster

James H Gilchrist

H Ray Jouett

Alan Kent Wilson

Andrew James Vetter

P J Thomas

Eduardo Gallas Cervo

Barry Brent Fish

C Calvert Churn, Iii

Donald L Morrison

Calvert C Churn

John Argyrolpoulos

Brent Fish

John Nicholas Argyrolpoulos

Ray H Jouett

Conditioning and concentration of microalgae are accomplished by the process steps of grinding a dilute aqueous dispersion of microalgae in the presence of grinding media and then applying adsorptive bubble separation. This process is amenable to the use of dilute feed microalgal dispersions such as are encountered in the production of algal biomass for biofuel applications.

Process for microalgae conditioning and concentration

Disclosed is a process for the extractive recovery of a homogeneous ruthenium catalyst from the reaction product of the hydrogenation of glycolic acid, glycolate esters, and/or glycolic acid oligomers with an extractant comprising a hydrophobic solvent and an optional hydrophilic solvent. The ruthenium catalyst, which can include 1,1,1-tris(diaryl- or dialkylphosphinomethyl)alkane ligands, can be recovered from the hydrophobic extract phase by back extraction with a hydrophilic solvent and recycled to a process for the preparation of ethylene glycol by the hydrogenation of glycolic acid and glycolic acid derivatives.

Method for recovery and recycle of ruthenium homogeneous catalysts

Disclosed is a process for the extractive recovery of an acid catalyst from an aqueous mixture of glycolic acid with an extraction solvent comprising a tertiary amine or an onium carboxylate compound, a modifier, and a diluent. The acid catalyst, which can comprise strong acids such as sulfuric acid, alkyl sulfonic acids, and fluoroalkyl sulfonic acids, can be recovered by back extraction with aqueous formaldehyde and recycled to a process for the preparation of glycolic acid by the acid-catalyzed carbonylation of formaldehyde. Also disclosed is a process for the preparation of glycolic acid by the acid-catalyzed hydrocarboxylation of formaldehyde.

Process for recovering and recycling an acid catalyst

Methods for recovery and recycle of ruthenium homogenous catalysts

Disclosed is a process for the extractive recovery of an acid catalyst from an aqueous mixture of glycolic acid with an extraction solvent comprising a tertiary amine or an onium carboxylate compound, a modifier, and a diluent. The acid catalyst, which can comprise strong acids such as sulfuric acid, alkyl sulfonic acids, and fluoroalkyl sulfonic acids, can be recovered by back extraction with aqueous formaldehyde and recycled to a process for the preparation of glycolic acid by the acid-catalyzed carbonylation of formaldehyde.

Process and apparatus are described for adsorptive bubble separation of hydrophobic particles from liquid dispersions. The process may be used to treat the gas/liquid dispersion after it has been introduced from two or more ducts near the perimeter or from a central duct of the separation vessel. When the gas-liquid-particle dispersion is introduced from a central duct, the rising bubbles are directed by, e.g., a baffle toward the perimeter of the apparatus, where they rise. At the liquid surface, bubbles with attached hydrophobic materials form a floating froth layer, which is directed toward a central froth collection launder. Rising froth at the perimeter pushing the froth bed into the reduced area of the center encourages further coalescence of the bubbles and increases liquid drainage from the froth, thus leading to concentration of the collected materials without the need for complex equipment geometry. Also disclosed is an improvement for froth flotation processes comprising using a vacuum to pull froth and/or collapsed froth into and through the froth collection launder and froth drain line. This improvement assists froth collection because froth can be pulled by suction through the collection system more easily than it can be drained by gravity.

Process and apparatus for adsorptive bubble separation

A method of concentrating particles in a liquid-particle dispersion feed by adsorptive bubble separation by intimately contacting a gas with a pressurized stream of liquid in a chamber to form an aerated dispersion that retains at least some of the kinetic energy from the pressurized stream, and removing at least some of the kinetic energy from the aerated dispersion to form a dense foam. A liquid-particle dispersion feed is then injected into the dense foam to form a gas-liquid-particle dispersion. The gas-liquid-particle dispersion is injected into a flotation chamber at a point below a surface of a liquid contained therein, where the gas-liquid-particle dispersion forms bubbles of a gas-particle agglomerate, and the bubbles are released from the feed liquid depleted in hydrophobic particles and rise to the surface to form a floating froth enriched in particles. Also described is a device that includes plurality of chambers for aeration and mixing, feed injection, and a duct that is positioned below the liquid-foam line of a flotation chamber, so that the gas-liquid-particle dispersion is released within the chamber, and rises to the surface as a floating froth enriched in particles.

Process and apparatus for adsorptive bubble separation using a dense foam

An aldehyde composition derived by hydroformylation of a transesterified seed oil and containing a mixture of formyl-substituted fatty acids or fatty acid esters having the following composition by weight: greater than about 10 to less than about 95 percent monoformyl, greater than about 1 to less than about 65 percent diformyl, and greater than about 0.1 to less than about 10 percent triformyl-substituted fatty acids or fatty acid esters, and having a diformyl to triformyl weight ratio of greater than about 5/1; preferably, greater than about 3 to less than about 20 percent saturates; and preferably, greater than about 1 to less than about 20 percent unsaturates.

Aldehyde compositions derived from seed oils

An aldehyde composition derived by hydroformylation of a transesterified seed oil and containing a mixture of formyl-substituted fatty acids or fatty acid esters having the following composition by weight: greater than about 10 to less than about 95 percent monoformyl, greater than about 1 to less than about 65 percent diformyl, and greater than about 0.1 to less than about 10 percent triformyl-substituted fatty acids or fatty acid esters, and having a diformyl to triformyl weight ratio of greater than about 5/1; preferably, greater than about 3 to less than about 20 percent saturates; and preferably, greater than about 1 to less than about 20 percent unsaturates. An alcohol composition derived by hydrogenation of the aforementioned aldehyde composition, containing a mixture of hydroxymethyl-substituted fatty acids or fatty acid esters having the following composition by weight: greater than about 10 to less than about 95 percent monoalcohol {mono(hydroxymethyl)}, greater than about 1 to less than about 65 percent diol {di(hydroxymethyl)}, greater than about 0.1 to less than about 10 percent triol, tri(hydroxymethyl)-substituted fatty acids or fatty acid esters; preferably greater than about 3 to less than about 35 percent saturates; and preferably, less than about 10 percent unsaturates. The alcohol composition can be converted into an oligomeric polyol for use in the manufacture of polyurethane slab stock flexible foam.

Aldehyde and alcohol compositions derived from seed oils

Disclosed is a process for the recovery of phosphorus and/or iodine containing catalyst components, present as an organophosphorus compound such as trihydrocarbylphosphine compounds and tetrahydrocarbylphosphonium compounds, from a solution of at least one such organophosphorus compound in an organic solvent by the steps comprising (1) converting the organophosphorus compound to an iodide complex of a organophosphonium compound which is insoluble in the organic solvent; and (2) separating the insoluble iodide complex of the organophosphonium compound from the solution. The process also results in the recovery of iodine values present in the solution.

Process for the recovery of phosphorus and iodine containing catalyst components

This invention relates to a process for separating one or more organophosphorus ligand degradation products, one or more reaction byproducts and one or more products from a continuously generated reaction product fluid comprising one or more unreacted reactants, a metal-organophosphorus ligand complex catalyst, optionally free organophosphorus ligand, said one or more organophosphorus ligand degradation products, said one or more reaction byproducts, said one or more products, one or more polar solvents and one or more nonpolar solvents by phase separation wherein (i) the selectivity of the polar phase for the organophosphorus ligand with respect to the one or more products is expressed by a partition coefficient ratio Ef1 which is a value greater than about 2.5, (ii) the selectivity of the polar phase for the organophosphorus ligand with respect to the one or more organophosphorus ligand degradation products is expressed by a partition coefficient ratio Ef2 which is a value greater than about 2.5, and (iii) the selectivity of the polar phase for the organophosphorus ligand with respect to the one or more reaction byproducts is expressed by a partition coefficient ratio Ef,which is a value greater than about 2.5.

Separation processes

This invention relates to a process for separating one or more organophosphorus ligand degradation products, one or more reaction byproducts and one or more formylester products from a reaction product fluid comprising one or more unreacted unsaturated ester reactants, a metal-organophoshorus ligand complex catalyst, optionally free organophosphorus ligand, said one or more organophosphorus ligand degradation products, said one or more reaction byproducts, said one or more products, a nonpolar solvent and a polar solvent by phase separation wherein (i) the selectivity of the nonpolar phase for the organophosphorus ligand with respect to the one or more products is expressed by a partition coefficient ratio Ef1 which is a value greater than about 2.5 (ii) the selectivity of the nonpolar phase for the organophosphorus ligand with respect to the one or more organophosphorus ligand degradation products is expressed by a partition coefficient ratio Ef2 which is a value greater than about 2.5, and (iii) the selectivity of the nonpolar phase for the organophosphorus ligand with respect to the one or more reaction byproducts is expressed by a partition coefficient ratio Ef3 which is a value greater than about 2.5.

Metal-ligand complex catalyzed processes

Growing community of inventors

Kingsport, TN, United States of America

Jeffrey Scott Kanel