Methods for producing supported catalysts containing a transition metal and a bound zeolite base are disclosed. These methods employ a step of washing the bound zeolite base in the presence of an alkali metal, prior to impregnating the bound zeolitic support with the transition metal. Alkali metals such as potassium and cesium may be used.

Methods for producing supported catalysts containing a transition metal and a bound zeolite base are disclosed. These methods employ a step of washing the bound zeolite base in the presence of an alkali metal, prior to impregnating the bound zeolitic support with the transition metal. Alkali metals such as potassium and cesium may be used.

A method for producing an organohalosilanes comprising reacting an organic compound comprising a halogen-substituted or unsubstituted alkane, a halogen-substituted or unsubstituted alkene, or an aromatic compound and at least one hydridohalosilane of formula R.sub.nSiH.sub.mX.sub.4-m-n, wherein each R is independently C-.sub.1-C-.sub.14 hydrocarbyl or C-.sub.1-C-.sub.14 halogen-substituted hydrocarbyl, X is fluoro, chloro, bromo, or iodo, n is 0, 1, or 2, m is 1, 2 or 3, and m+n=1, 2 or 3, in the presence of a heterogeneous catalyst comprising an oxide of one or more of the elements Sc, Y, Ti, Zr, Hf, B, Al, Ga, In, C, Si, Ge, Sn, or Pb, at a temperature greater than 100 C., and at a pressure of at least 690 kPa, to produce a crude reaction product comprising the organohalosilane.

Regenerable aromatization catalysts having high surface area and pore volume, as well as methods for producing these catalysts, are disclosed.

The present invention relates to a method for fluorinating a chlorinated compound including the steps of (a) placing said chlorinated compound in contact with gaseous hydrogen fluoride within a reactor and in the presence of a fluorination catalyst to produce a fluorinated compound, and (b) regenerating the fluorination catalyst used in step a), the step of regenerating the fluorination catalyst including (c) treating said fluorination catalyst with an oxidizing agent to form an oxidized fluorination catalyst, and (d) treating the oxidized fluorination catalyst obtained in step (c) with a gas mixture including a reducing agent.

Disclosed herein are methods of improving the life of high selectivity, silver catalysts for making ethylene oxide. Ethylene and oxygen are reacted over the high efficiency catalyst with at least one organic chloride modifier, and during a catalyst aging period of no less than 0.03 kt ethylene oxide/cubic meter catalyst, the overall catalyst chloriding effectiveness never exceeds an efficiency-maximizing optimum overall catalyst chloriding effectiveness value that corresponds to a reference feed gas composition and a set of reference reaction condition values. Reaction temperature and/or feed gas oxygen concentration are adjusted to obtain or maintain a desired value of an ethylene oxide production parameter. Once the reaction temperature and/or oxygen concentration vary by a specified amount from their respective reference values in the set of reference reaction condition values, the overall catalyst chloriding effectiveness is changed to account for a shift in the optimum (efficiency-maximizing) value.

Disclosed herein are methods of improving the life of high selectivity, silver catalysts for making ethylene oxide. Ethylene and oxygen are reacted over the high efficiency catalyst with at least one organic chloride modifier, and during a catalyst aging period of no less than 0.03 kt ethylene oxide/cubic meter catalyst, the overall catalyst chloriding effectiveness never exceeds an efficiency-maximizing optimum overall catalyst chloriding effectiveness value that corresponds to a reference feed gas composition and a set of reference reaction condition values. Reaction temperature and/or feed gas oxygen concentration are adjusted to obtain or maintain a desired value of an ethylene oxide production parameter. Once the reaction temperature and/or oxygen concentration vary by a specified amount from their respective reference values in the set of reference reaction condition values, the overall catalyst chloriding effectiveness is changed to account for a shift in the optimum (efficiency-maximizing) value.

A method of preparing an aromatization catalyst comprising contacting a zeolitic support with a metal-containing compound and a boron-containing compound to produce an impregnated support, and contacting the impregnated support with an activating composition to produce an aromatization catalyst, wherein the activating composition comprises a chlorine-containing compound and a fluorine-containing compound, and wherein the impregnated support is heated in the presence of the activating composition to a temperature in the range of from about 100 C. to about 500 C.

A method of preparing an aromatization catalyst comprising contacting a zeolitic support with a metal-containing compound and a boron-containing compound to produce an impregnated support, and contacting the impregnated support with an activating composition to produce an aromatization catalyst, wherein the activating composition comprises a chlorine-containing compound and a fluorine-containing compound, and wherein the impregnated support is heated in the presence of the activating composition to a temperature in the range of from about 100 C. to about 500 C.

The invention relates to a method to start up a Fischer-Tropsch process. A catalyst with a latent activity is used. The catalyst comprises titania, cobalt, promoter, and chlorine. The catalyst comprises more than 0.7 and less than 4 weight percent of the element chlorine, calculated on the total weight of the catalyst.