Air Products and Chemicals, Inc.

Arco Chemical Technology, L.p.

Bayer Antwerp, N.v.

Susan M Clift

Jeremiah P Casey

Nigel Barksby

Kenneth Merle Kem

Barton Milligan

Bruce D Lawrey

Kevin Rodney Lassila

Michael E Ford

William Edward Starner

William A Gill

David J Ho

Elastomers with improved physical properties, particularly hardness, resilience, tear strength, and compression set, may be prepared by the chain extension or moisture cure of isocyanate-terminated prepolymers prepared from a polyol component comprising a high molecular weight, low unsaturation polyoxypropylene diol and a low molecular weight diol. The elastomers are useful for applications such as rollers and other applications for which these physical properties are important.

Polyurethane and polyurethane/urea heat-cured and moisture-cured elastomers with improved physical properties

Microcellular polyurethane elastomer shoe sole components have exceptional physical properties may be prepared from isocyanate-terminated prepolymers derived from polyoxypropylene diols having a molecular weight of from about 2000 Da to 8000 Da, an unsaturation less than about 0.02 meq/g, and a random oxyethylene content of from about 5 to about 15 weight percent. The shoe sole components exhibit high tensile strength, elongation, resilience, and in addition have excellent tear strength, particularly 90.degree. angle tear.

Microcellular elastomers with improved processability and properties

Elastomers with improved physical properties, particularly hardness and rebound, may be prepared by the diamine chain extension or moisture cure of low isocyanate group content, toluene diisocyanate-based prepolymers prepared from a polyol component comprising a high molecular weight, low unsaturation polyoxypropylene diol and a low molecular weight diol. The elastomers are useful for applications such as rollers and other applications where hardness and rebound are important.

Polyurethane/urea heat-cured and moisture-cured elastomers with improved

This invention relates to o-tolidines which have a tert-butyl substituent ortho to an amine group. These compositions are represented by the formula: ##STR1## where R.sub.1 =i-propyl, or t-butyl, and where R.sub.2 =hydrogen, i-propyl, or t-butyl. The compositions are useful in the preparation of polyepoxide resins as well as polyurethanes, polyamides and polyimides.

Ortho-alkylated tolidines

The present invention relates to a process for the production of polyurethanes wherein a tertiary amine functionality is incorporated into the side chain of an aromatic diamine, preferably a diaminobenzamide, to form a catalytic polyurethane chain extender. These chain extenders are polyurethane catalysts that provide adequate cure without residual odor and safety hazards associated with the more traditional tertiary amine catalysts. When reacted with the isocyanate reactive group the non-tertiary amine portion of the chain extender is bound to the polymeric network. Diffusion of the catalyst species from the polyurethane has been prevented, thus negating odor and toxicity as problems. These aromatic diamines provide enhanced polyurethane physical properties.

Aromatic diamine catalytic chain extenders

The present invention relates to a process for the production of polyurethanes wherein a tertiary amine functionality is incorporated into the side chain of an aromatic diamine, preferably a diaminobenzamide, to form a catalytic polyurethane chain extender. These chain extenders are polyurethane catalysts that provide adequate cure without residual odor and safety hazards associated with the more traditional tertiary amine catalysts. When reacted with the isocyanate reactive group the non-tertiary amine portion of the chain extender is bound to the polymeric network. Diffusion of the catalyst species from the polyurethane has been prevented, thus negating odor and toxicity as problems. The aromatic diamine provides enhanced polyurethane physical properties.

The present invention relates to a process for the production of polyurethanes wherein a tertiary amine functionality is incorporated into the side chain of a diaminobenzoate to form catalytic polyurethane chain extender. These chain extenders are polyurethane catalysts which provide adequate cure without residual odor and safety hazards associated with the more traditional tertiary amine catalysts. When reacted with the isocyanate reactive group the non-tertiary amine portion of the chain extender is bound to the polymeric network thereby preventing diffusion of the catalyst species from the polyurethane and negating odor and toxicity as problems. The diaminobenzoate provides enhanced polyurethane physical properties.

Diaminobenzoate catalytic chain extenders

The present invention relates to polyurethanes and a method for making polyurethanes by reacting an organic diisocyanate, a glycol having a molecular weight of 500-5000 and a derivative of 2,6-diaminobenzoic acid or a blend comprising derivatives of 2,4-diaminobenzoic acid and 2,6-diaminobenzoic acid. The addition of the 2,6-diaminobenzoic acid derivative to the composition improves polyurethane processability and performance by decreasing chain extender reactivity and increasing hard segment regularity.

Process of preparing polyurethanes cured with 2,6-idaminobenzoic acid

This invention relates to a polyisocyanate prepolymer for polyurethane/urea elastomer synthesis and to the resulting elastomer. The prepolymer is formed by reacting toluenediisocyanate with a long chain polyol under conditions such that essentially a 2:1 adduct is formed. Excess toluenediisocyanate is removed prior to forming the elastomer.

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Lansdale, PA, United States of America

Susan M Clift