Lyondell Chemical Technology, L.p.

Arco Chemical Technology, L.p.

Olin Corporation

Peter J Whitman

Stephen L Goldstein

Robert N Cochran

Jay F Miller

Roger A Grey

Stephen Herbert Harris

Daniel B Pourreau

Bernard Cooker

Kun Qin

James M O'Connor

Augustin T Chen

Donald L Lickei

Benjamin W Tucker

Edward A Barsa

Henry G Barnowski, Jr

Allen B Quakenbush

Willard F Burt

John H Speidel, Jr

Buford T Pennington

Jeffrey W Baird

Chunjie Zhang

A process for producing an epoxide comprising reacting an olefin, hydrogen and oxygen in the presence of a catalyst comprising a titanium or vanadium zeolite, palladium, and lead. The process results in significantly reduced alkane by-product formed by the hydrogenation of olefin.

Direct epoxidation process using improved catalyst composition

The invention is a catalyst comprising a titanium or vanadium zeolite, a binder, and zinc oxide, wherein the catalyst is preparing an aqueous mixture of the zeolite, a binder source, and a zinc oxide source, and subjecting the mixture to rapid drying. The catalyst is useful in olefin epoxidation.

Epoxidation catalyst

The invention is a process for epoxidizing an olefin with hydrogen and oxygen in the presence of a catalyst comprising a noble metal and a titanium or vanadium zeolite in a solvent mixture comprising water, methanol, and a C&#x2013;Caliphatic ketone. This process surprisingly gives significantly reduced by-product glycol and glycol ethers formed by the unwanted ring-opening of epoxides.

Direct epoxidation process

Titanium or vanadium zeolites are pretreated by contacting with an amino polyacid compound, such as ethylenediaminetetraacetic acid or a salt thereof, prior to use in olefin epoxidation with hydrogen peroxide.

Allyl carbamates are disclosed. The allyl carbamates are prepared by reacting an isocyanate with an allylic alcohol or alkoxylated allylic alcohol. Suitable isocyanates are selected from hexamethylene diisocyanate (HDI), HDI biuret, dimer, HDI trimer, HDI allophanate, isophorone diisocyanate (IPDI), IPDI trimer, IPDI allophanate, bis(isocyanatocyclohexyl)methane, and mixtures thereof. The allyl carbamates have at least two allyl functional groups per molecule. UV-curable and air-drying coatings formulated from the allyl carbamates show excellent chemical resistance and physical properties.

Multifunctional allyl carbamates and coatings therefrom

A multi-step process for producing DNT employing a mononitration step in a single liquid phase at an elevated temperature using a carefully controlled amount of water, followed by a phase separation step prior to dinitration of the MNT present in the resulting organic phase. This process results in a DNT product with a desired isomer ratio of 2,4-DNT to 2,6-DNT and provide relatively fast nitration rates with less by-products.

Two-stage dinitrotoluene production process

Disclosed are new coatings compositions based on an HDI isocyanurate or biuret polyisocyanate and a bis(imine) reaction product of a diaminoalkane containing between two and five carbon atoms with an alkyl aldehyde containing between four and seven carbon atoms (advantageously a bis(imine) product of the reaction of 1,4-diaminobutane and isobutyraldehyde). The latter bis(imine) is completely miscible in HDI isocyanurate and biuret polyisocyanates, and, as a reactive diluent, allows the preparation of high performance coatings formulations that require only small amounts of solvents to achieve a conveniently sprayable viscosity.

Bis(isobutyraldimine) of 1,4-diaminobutane in HDI trimer and

A process for increasing the rate of catalytic hydrogenation of aromatic amines by reacting aromatic amines with hydrogen in the presence of a noble metal catalyst, a water miscible organic solvent, lithium hydroxide catalyst promoter, and water in an effective amount to increase the rate of the hydrogenation reaction without an appreciable increase in total amounts of by-products.

Method of increasing hydrogenation rate of aromatic amines

A process for increasing the rate of catalytic hydrogenation of aromatic amines by reacting aromatic amines with hydrogen in the presence of a noble metal catalyst, an organic solvent or a mixture of solvents, and at least one salt of a transition or lanthanide metal as a promoter, in an effective amount to increase the rate of the hydrogenation reaction, decrease the induction period, and decrease the amount of higher boiler by-products.

Growing community of inventors

Glen Mills, PA, United States of America

Peter J Whitman