Angus Chemical Company

Dow Global Technolgoies LLC

G David Green

Raymond John Swedo

Patrick E Brutto

John L Pohlman

Asghar Akber Peera

James P Godschalx

Charles Coburn

David W Moore

Mahesh Sawant

Sheila M Tinetti

Shreyas Bhide

Chunzhao Li

Bonnie A Pyzowski

John W Quinn

Esin G Busche

The present technology relates generally to aqueous dispersion or emulsion compositions that include a polymeric binder resin and an ether amine. Specifically, the polymeric binder resin includes acid functional groups, at least a portion of which are neutralized by the ether amine such that the polymeric binder resin is dissolved or dispersed in the water, provided that the polymeric binder resin is not a polyurethane and the ether amine is a compound of formula I: wherein Rand Rare independently C-Calkyl or C-Ccycloalkyl group; or Rand R, together with the nitrogen to which they are attached, form a C-Cmembered heterocycloalkyl ring; A is a C-Calkylene or C-Ccycloalkylene ring; and Ris C-Calkyl or C-Ccycloalkyl group; provided that the compound of formula I contains no more than 10 carbons. 

Ether amine compositions and coatings

Provided are aminoalcohol compounds for use as additives for paints and coatings. The compounds are of the formula (I): wherein x, R, R, R, R, R, R, R, and Rare as defined herein. 

Aminoalcohol compounds and their use as zero or low VOC additives for paints and coatings

A process of preparing a nitroalcohol, e.g., 2-nitro-2-methyl-1-propane, from a nitropolyol, e.g., 2-nitro-2-methyl-1,3-propanediol, the process comprising the step of contacting under hydrogenation conditions the nitropolyol with hydrogen, a hydrogenation catalyst and, optionally, a chelating agent.

Process for the preparation of nitroalcohols

Biocidal compositions and their use in aqueous media, such as metalworking fluids, the compositions comprising a biocidal agent; and a non-biocidal primary amino alcohol compound of the formula (I): wherein R, R, R, R, and Rare as defined herein. 

Aminoalcohol and biocide compositions for aqueous based systems

Provided are additives of formula I for use in hydrocarbonaceous compositions, such as petroleum or liquid fuels: (I) wherein R1, R2, R3, R4, and R5 are as defined herein. The additives improve the corrosion resistance of the compositions. The additives also enhance the antimicrobial efficacy of any added biocides contained in such compositions. 

Corrosion and microbial control in hydrocarbonaceous compositions

A process for preparing isoxazole compounds of formula I: in which a nitroaryl of the formula (II): is contacted with an alkyl acetoacetate of the formula (III) or a salt thereof: in the presence of an activating agent and a base to provide the isoxazole compound.

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Cary, IL, United States of America

G David Green