Wiley Organics, Inc.

Central Soya Company, Inc.

Lignan Research, LLC

Thomas A Dobbins

David B Wiley

Arthur H Konwinski

Deborah C Hurst

Reduced toxicity fuels containing hydrocarbons having both strained rings and internal, conjugated triple bonds are disclosed. The fuels described herein are hypergolic with nitrogen tetroxide and/or inhibited red fuming nitric acid.

Hypergolic hydrocarbon fuels

Novel catalysts capable of rendering both polar and non-polar organic fuels hypergolic with rocket-grade hydrogen peroxide are disclosed. These catalysts are complexes formed by reacting alkyl-substituted diamines or triamines, with metal salts of an aliphatic carboxylic acid or metal 1,3 dione chelates. In addition, the use of various acetylenic compounds as stability enhancing additives and/or promoters is described.

Catalyst system for rendering organic propellants hypergolic with hydrogen peroxide

A process for enriching the relative concentration of genistin from a mixture of isoflavones is described. In accordance with one aspect of the invention, the process comprises providing a material containing a mixture of isoflavones, extracting the material with an aqueous organic solvent solution, adding calcium oxide or calcium hydroxide to the extract to form calcium-isoflavone complexes and separating precipitated calcium-isoflavone complexes from the extract. The precipitated calcium-isoflavone complexes contain a higher concentration of genistin complexes than daidzin and glycitin complexes.

Process for isolating genistin from mixtures of soy isoflavones

A process for extracting secoisolariciresinol diglycoside (SDG) from de-fatted flaxseed is described. The process comprises contacting defatted flaxseed with an extraction solvent of acetone and water, extracting the de-fatted flaxseed with the extraction solvent to extract SDG-containing compounds, removal of solvents, followed by alkaline hydrolysis of the extract to liberate free SDG or its salts.

Process for recovering secoisolariciresinol diglycoside from de-fatted flaxseed

A novel process for making an isoflavone concentrate product from soybeans which includes diluting solubles from alcohol-extracted hexane-defatted soybean flakes to about 10% to about 30% solids, separating undissolved solids from the diluted soy solubles, such that the separated solids have at least 4% isoflavones by weight of dry matter. That concentrate can then be further concentrated to at least 40% isoflavones by weight of dry matter by adjusting pH and temperature and extracting with solvents. The soy isoflavone concentrate products are then used in a liquid or dry beverage, food or nutritional products.

Soy isoflavone concentrate process and product

This invention uses acetone/water mixtures at various concnetration and temperatures as a cost effective method for recoveing soy saponins of high purity from soybean-derived materials, while also affording an economical means of recovering soy isoflavones as a by-product.

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Howard, OH, United States of America

Thomas A Dobbins