Mobil Oil Corporation

Weldon K Bell

Werner O Haag

Clarence D Chang

Mohsen N Harandi

Jeffrey C Trewella

Hartley Owen

Stephen Harold Brown

Costandi A Audeh

Garry W Kirker

Donald J Klocke

Scott S Han

David O Marler

Tracy J Huang

Robert A Ware

Hye Kyung Timken

Chaya R Venkat

Reuel Shinnar

Ying-Yen P Tsao

Robert E Palermo

Minas R Apelian

Rudolph M Lago

James H Beech, Jr

Anthony S Fung

D Duayne Whitehurst

Frederick Earl Daugherty

Steven H Brown

W Thomas Mo

A condensation reaction process and reactor for converting a plurality of reactants to at least one reaction product having a vapor pressure less than the vapor pressure of the reactants. The process includes heating a liquid phase of the reactants to at least partial vaporization thus forming a vapor phase of the reactants. The vapor phase reactants are passed in a vapor and or condensed state through at least one catalyst bed spaced from the liquid state to form reaction product(s). The reaction product(s) is returned to the liquid phase without additional contact with catalyst.

Vapor pocket reactor

A multistaged fixed catalyst bed process for the production of diisopropyl ether and isopropanol is disclosed comprising a fixed bed of serially connected stages containing zeolite Beta catalyst. A feedstream of propylene and water equivalents selected from the group consisting of water, isopropanol and diisopropyl ether is introduced into each stage at a rate sufficient to provide a mole ratio of water equivalents to propylene equivalents that increases in increments by stage from at least 0.1 in a first stage to at most 1.2 in a final stage. The feedstream is introduced at a temperature between 50.degree. and 450.degree. C., pressure between 700 and 24000 kPa, and weight hourly space velocity between 0.10 and 30, based on catalyst, whereby a single non-aqueous liquid phase is maintained in the fixed bed. An effluent product stream is recovered comprising diisopropyl ether, isopropanol and water from the final stage. Isopropanol is recycled to the first stage when the preferred product is diisopropyl ether. When the preferred product is isopropanol, diisopropyl ether and water are recycled to the first stage.

Multistage indirect propylene hydration process for the production of

A process for catalytic cracking and C3/C4 olefin alkylation with phosphorus stabilized faujasite catalyst is disclosed. Catalytic cracking produces C3 and C4 olefins, which are alkylated using phosphorus stabilized and water activated cracking catalyst. Spent alkylation catalyst may be discharged into the FCC unit.

Alkylation with activated equilibrium FCC catalyst

Porous metallosilicate catalyst (e.g. Zeolite Beta) is active at low temperature for converting lower alkanol (e.g. methanol) and C.sub.4 -C.sub.7 tertiary alkenes to high octane ether product. Such catalytic reaction is especially useful in multizone catalytic reactor systems employing catstill rectification.

Multizone catalytic process

An olefin hydration catalyst is regenerated with a non-oxidizing light gas, such as hydrogen. Light olefins, especially propylene, are converted to a mixture of alcohol(s), such as isopropanol (IPA) and ether(s), such as diisopropylether (DIPE) by contacting a feed containing the olefin with water and/or alcohol with the olefin hydration catalyst. Regeneration conditions include temperatures of from about 150.degree. C. to about 550.degree. C., pressures below about 1000 psig (6900 kPa). Lower pressures of regeneration unexpectedly demonstrated more effective catalyst regeneration through greater coke removal.

Olefin conversion catalyst regeneration

A process for catalytically converting cyclohexanone oxime to epsilon caprolactam. The conversion catalyst is a crystalline aluminosilicate zeolite having a Constraint Index greater than 1 and a reduced surface acidity. The surface acidity is reduced by selective surface dealumination of the crystalline aluminosilicate zeolite by contacting the zeolite with dicarboxylic acid, such as oxalic acid.

Synthesis of caprolactam using catalysts

A process is disclosed for the production of alkyl tertiary alkyl ether from alkanol and iso-olefin employing zeolite catalyst, particularly zeolite Beta, that results is a high ether selectivity and a significant reduction in the formation of olefin oligomer by-product. The improvement is realized by incorporating a catalyst pretreatment step in the overall etherification process. The zeolite catalyst pretreatment comprises either steaming or a hydrothermal treatment using liquid water at elevated temperature. The process is particularly effective in reducing the formation of dimer by-product in the zeolite Beta catalyzed process for the formation of MTBE with high selectivity.

Production of tertiary alkyl ether using improved zeolite catalyst

A process for synthesizing di-isopropyl ether (DIPE) by etherification of isopropanol. A multi-stage process can employ propene in mixture with other feedstock materials, such as propane from refinery gas, in a primary hydration stage to produce isopropanol. The isopropanol is enriched between stages to remove water. In the second reaction stage the isopropanol is converted catalytically with large pore acidic zeolite to yield DIPE, which can be separated to recover pure propene.

Ether production

A process is disclosed for converting a light hydrocarbon feedstock that contains a mixture of linear and branched olefins to ether-rich high octane gasoline streams that include tertiary alkyl and isoalkyl ethers such as MTBE, TAME, methyl isopropyl ether (MIPE), and methyl sec-butylether (MSBE). The conversion is achieved by utilizing the differing reactivity of tertiary olefins under selected conditions compared to linear olefins in the catalyzed etherification processes. The discovery has been made that unreacted olefins from the etherification reactions can be converted to gasoline boiling range hydrocarbons by contacting them with zeolite catalyst at elevated temperature. Further, it has been discovered that unreacted paraffins in the integrated process can be dehydrogenated to produce C.sub.3 -C.sub.4 olefins which can be recycled to the etherification process.

Conversion of light hydrocarbons to ether rich gasoline

A novel Fischer Tropsch iron catalyst that has unusually high selectivity for liquid hydrocarbons (low selectivity for methane) is provided. The catalyst is prepared by treatment of the usual inactive catalyst precursor with water vapor at elevated temperature either after conventional activation by syngas or concurrently therewith. Surprisingly, the 'selectivation' with water vapor does not affect catalytic activity. The novel 'selectivated' catalyst may be used to advantage either to increase temperature and throughput, or to increase liquid hydrocarbon selectivity, compared with conventional catalyst that has not been 'selectivated'.

Method for preparing a promoted iron catalyst and catalyst prepared by

The medium pressure Fischer-Tropsch synthesis of liquid hydrocarbons conducted with an iron catalyst is made more efficient by temporarily suspending conventional synthesis and treating the catalyst with a high partial pressure of water vapor, after which conventional synthesis is resumed. The treatment inparts a large increase in selectivity for liquids with reduction of methane formation. The treatment is very effective with alkali (e.g. potassium) promoted precipitated iron catalyst.

Conversion of synthesis gas to liquid hydrocarbons

There is provided a process for converting methane to carbon disulfide. More particularly, methane is decomposed to form elemental carbon and elemental hydrogen, and the elemental carbon is reacted with sulfur to form carbon disulfide. Carbon disulfide may then be contacted with hydrogen, optionally in the presence of more methane, under conditions sufficient to produce CH.sub.3 SH. This CH.sub.3 SH may then be contacted with a sufficient catalyst, such as a zeolite, especially ZSM-5, under conditions sufficient to produce hydrocarbon having two or more carbon atoms.

Cyclic process for converting methane to carbon disulfide

Olefin is etherified with alcohol to provide an ether or mixture of ethers employing catalyst comprising zeolite characterized by an X-ray diffraction pattern including interplanar d-spacings at 12.36+0.4, 11.03+0.2, 8.83.+-.0.14, 6.18.+-.0.12, 6.00.+-.0.10, 4.06.+-.0.07, 3.91.+-.0.07 and 3.42.+-.0.06 Angstroms.

Process for preparing ethers

A process is provided for catalytically converting cyclohexanone oxime to epsilon caprolactam. The conversion is characterized by exceptionally high selectivity and reduced rate of catalyst aging, even at single pass conversion above 90 percent. The conversion catalyst is a medium pore size crystalline zeolite exemplified by ZSM-5 which has low acid activity. Recycling unconverted oxime provides excellent ultimate yield of caprolactam.

Synthesis of caprolactam

There is provided a process for converting methane to higher molecular weight hydrocarbons. In a first step, methane is contacted with elemental sulfur under conditions sufficient to produce carbon disulfide. Carbon disulfide from this step is then contacted with methane and hydrogen under conditions sufficient to convert methane and to produce CH.sub.3 SH. This CH.sub.3 SH is then contacted with a sufficient catalyst, such as a zeolite, especially ZSM-5, under conditions sufficient to produce hydrocarbons having two or more carbon atoms.

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Pennington, NJ, United States of America

Weldon K Bell