American Cyanamid Company

Cytec Technology Corporation

Other

American Cyanamid

David A Ley

Larry S Anderson

Laurence W Chang

Ram Baboo Gupta

Lawrence A Flood

Revathi Iyengar

Vankatarao K Pai

Herbert Burkhard

Susan Mancini Cady

Michael T Cooke

Howard R Lucas

Denise Elizabeth Fiori

Richard J Quinn

Laura J Hiscock

Venkatarao K Pai

Robert Gerald Lees

Provided is a process for preparing an at least bis-carbamate functional 1,3,5-triazine by contacting an at least diamino-1,3,5-triazine, an acyclic organic carbonate and a base, as well as certain novel compositions producible thereby. Also provided are substantially halogen contamination free crosslinker compositions comprising the products obtainable by the process, and curable compositions based upon these crosslinkers.

Process for the preparation of 1,3,5-triazine carbamates from amino-1,3,5-triazines and organic carbonates

Provided is a low volatile organic content (VOC), isocyanate based curable oil-in-water emulsion of a polyisocyanate crosslinker and a surface active isocyanate reactive material in an aqueous medium, and a process for the preparation thereof. Also provided is a water-in-oil intermediate product to which an aqueous medium can be added to produce the curable oil-in-water emulsions. Such curable emulsions are particularly suited for use in coatings applications.

Low VOC, isocyanate based aqueous curable compositions

1,3,5-Triazine carbamates from amino-1,3,5-triazines and organic carbonates and curable compositions thereof

Provided is a novel carbamate functional 1,3,5-triazine of the general formula ##STR1## wherein Z' is selected from the group consisting of hydrogen, hydrocarbyl, and a group represented by the formula NHQ',

Carbamate functional 1,3,5-triazines

New and improved curable compositions useful as non-yellowing, acid resistant coatings for a variety of substrates and as adhesives and binders are disclosed. The curable compositions comprise a polymeric component comprising poly(C.sub.1 -C.sub.6 alkyl acrylamidoglycolate) functional units and poly (active hydrogen) functional units and preferably an effective amount of a protic acid crosslinking catalyst. In preferred embodiments acid-catalyzed room temperature curable coating compositions are provided. The compositions may be cured effectively at lower temperatures without the use of amines or other toxic crosslinking agents and do not liberate formaldehyde on curing. A method for making poly(C.sub.1 -C.sub.6 alkyl acrylamidoglycolate) functional polymers is also disclosed.

Polymeric curable compositions containing alkylacrylamidoglycolates

Process for the preparation of 1,3,5-triazine carbamates from amino

Process for the preparation of 1,3,5-triazine carbamates from

A bead composition is disclosed herein which comprises a core of a polyacrylonitrile homopolymer or copolymer and a surface of pendant N-haloamide groups. Also disclosed is a process for the production of said composition.

Surface-modified polyacrylonitrile beads

A porous shaped substrate such as a porous bead is formed from polyacrylonitrile or a copolymer thereof containing nitrile groups. The substrate has a hydrophilic surface containing amide groups constituting about 1.8 mole percent to less than about 15 mole percent of the total nitrile groups, and containing no amide or carboxyl groups. The substrate is substantially non-swellable in water and is able to resist pressures in a columnar bed of up to about 3000 psi without collapsing. In forming the amide groups, polyacrylonitrile or copolymer thereof containing nitrile groups, an alkaline catalyst such as sodium hydroxide and a nonsolvent for the substrate such as methanol are combined to form a suspension. A peroxide is added to the suspension and the suspension is heated to hydrolyze nitrile groups to amide groups. Succinylated aminoethyl groups or activated carboxyl groups can be formed on the substrate and a bioactive ligand such as p-aminobenzamidine covalently bonded to the substrate. The bound ligand can then be used to complex a biologically active substance such as an enzyme to separate the substance from solution.

Porous acrylonitrile polymer substrate for bonding ligands and

A surface-modified fibrillated fiber composition is disclosed herein which comprises polyacrylonitrile homopolymer or copolymer and a surface of pendant N-haloamide groups. Also disclosed is a process for the production of said composition.

Surface-modified polyacrylonitrile fibrous substrates

A composition is disclosed herein which comprises a core of a polyacrylonitrile homopolymer or copolymer and a surface of N-haloamides. Also disclosed is a process for the production of said composition.

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New Canaan, CT, United States of America

David A Ley