A method for producing a hydroisomerization catalyst includes a first step of preparing a support precursor by heating a mixture containing an ion-exchanged zeolite and a binder, the ion-exchanged zeolite being prepared by ion-exchanging an organic template-containing zeolite which contains an organic template and has a one-dimensional pore structure including a 10-membered ring in a solution containing ammonium ions and/or protons, at a temperature of 250 to 350° C. under N.sub.2 atmosphere, and a second step of preparing a hydroisomerization catalyst, which is prepared by calcining a catalyst precursor, the catalyst precursor being prepared based on the support precursor containing a platinum salt and/or a palladium salt, at a temperature of 350 to 400° C. in an atmosphere containing molecular oxygen, the hydroisomerization catalyst containing a support which includes a zeolite and carries platinum and/or palladium.

The present invention relates to a catalyst for preparing a light olefin, a preparation method therefor, and a method for preparing a light olefin by using same, and can provide a catalyst for preparing a light olefin, a preparation method therefor, and a method for preparing a light olefin by using same, the catalyst comprising a porous zeolite, a clay, an inorganic oxide binder, and Ag.sub.2O and P.sub.2O.sub.5 which are supported in the pores and/or on the surface of the porous zeolite.

A process is provided for the catalytic cracking of a glyceride oil feedstock with a catalyst composition containing a deactivated phosphorus-containing ZSM-5 light olefins selective additive.

A process includes reacting a feed stream containing ethanol and optionally acetaldehyde in a dehydration reactor in the presence of a dehydration catalyst system having a Group 4 or Group 5 metal oxide and a support. The process includes obtaining a product stream containing butadiene from the dehydration reactor. Another process includes reacting a feed stream containing ethanol and optionally acetaldehyde in a dehydration reactor in the presence of a dehydration catalyst system containing a tungsten oxide supported on a zeolite or a tantalum oxide supported on a zeolite. The process includes obtaining a product stream containing butadiene from the dehydration reactor.

Isomerizing dehydration of feedstock containing a primary alcohol substituted in position 2 by an alkyl group in which the feedstock is heated to the reaction temperature by indirect heat exchange then vaporization by mixing with a diluent effluent, the diluted and vaporized feedstock being dehydrated in at least one dehydration reactor operating in gas phase at an inlet temperature comprised between 250 and 375° C., at a pressure comprised between 0.2 MPa and 1 MPa and at a WHSV comprised between 1 and 18 h.sup.−1, in the presence of a catalyst comprising a zeolite having at least one series of channels the opening of which is defined by a ring with 8 oxygen atoms (8MR) and a binder, the catalyst being coked beforehand in-situ or ex-situ, so as to produce a dehydration effluent, the latter being treated and separated into a diluent effluent, an alkenes effluent and a heavy hydrocarbons effluent.

A method of selectively catalysing the reduction of oxides of nitrogen (NO.sub.x) including nitrogen monoxide in an exhaust gas of a stationary source of NO.sub.x emissions also containing oxides of sulfur (SO.sub.x) comprising the steps of passively oxidising nitrogen monoxide to nitrogen dioxide (NO.sub.2) over an oxidation catalyst comprising a platinum group metal so that a NO.sub.2/NO.sub.x content is from 40-60%; introducing a nitrogenous reductant into the exhaust gas; and contacting exhaust gas having the 40-60% NO.sub.2/NO.sub.x content and containing the nitrogenous reductant with a selective catalytic reduction (SCR) catalyst comprising an aluminosilicate zeolite promoted with copper.

A method for preparing a molecular sieve SCR (selective catalytic reduction) catalyst and a prepared catalyst therethrough. In the method, several molecular sieves are mixed and modified by transition metal or rare-earth metal via ion exchange, then loaded Fe by equivalent-volume impregnation, and loaded Cu by one or more liquid ion exchange. This present invention, combined with several techniques, such as modification of stable molecular sieve by transition and rare-earth metal, Fe loading by equivalent-volume impregnation and Cu loading by one or more liquid ion exchange, and after through stable and effective modification and loading control, the obtained catalyst material is coated on a carrier substrate via size mixing and coating process to be prepared into an integral catalyst.

The invention relates to a process for combined ethylbenzene reforming and xylene isomerisation comprising contacting a hydrocarbon feedstock containing ethylbenzene and xylene with a catalyst comprising a catalyst carrier and one or more metal(s) supported on the catalyst carrier, wherein the catalyst carrier is an extrudate comprising (i) a ZSM-48 and/or EU-2 type zeolite and (ii) an alumina binder, the extrudate having a shape with a C/A value of at least 3, where C is the circumference of the extrudate and A is the cross-sectional area of the extrudate. The metal may be platinum and the alumina may be a wide-pore alumina. The process displays high conversion rates whilst maintaining low levels of side-product formation.

A process is disclosed for producing distillate range hydrocarbons using MTW and/or SSZ-41x catalysts.

A process for isomerizing an aromatic cut containing at least one aromatic compound containing eight carbon atoms per molecule is described, comprising bringing said cut into contact with at least one catalyst comprising at least one metal from group VIII of the periodic classification of the elements, at least one zeolitic support comprising a zeolite selected from zeolites with structure type EUO and MOR, used alone or as a mixture, and at least one matrix, such that the specific surface area of the matrix in the zeolitic support of said catalyst is in the range 5 to 200 m.sup.2/g.