The present invention relates to a method of preparing butadiene. More particularly, the present invention relates to a method of preparing butadiene by feeding butene and oxygen into a reactor containing a composite metal oxide catalyst and performing oxidative dehydrogenation, wherein a mole ratio of the oxygen to the butene is 1.8 to 2.2. In accordance with the present invention, a method of preparing butadiene to secure long-term operation stability by maintaining the intensity of a catalyst despite oxidative dehydrogenation and not to decrease selectivity due to less side reaction is provided.

A methanation reaction catalyst for methanation by allowing carbon dioxide to react with hydrogen, wherein the methanation reaction catalyst includes a stabilized zirconia support having a tetragonal crystal structure and in which Ca and Ni are incorporated in the crystal structure, and Ni in the metal state supported on the stabilized zirconia support, includes the following in atomic % based on metals in the element state, A) Zr composing the stabilized zirconia support: 6 to 62 atomic %, B) Ca incorporated in the crystal structure: 1 to 20 atomic %, and C) a total of Ni incorporated in the crystal structure and Ni supported on the stabilized zirconia support: 30 to 90 atomic %, and the atomic ratio of Ca/(Zr+Ca) is 0.14 to 0.25.

A catalyst for catalytic reactors of which the outer shape is a helix with n blades, where n is greater than or equal to 1, wherein the stack void fraction percentage is between 75% and 85% and the surface area/volume ratio is greater than 1000 square meters/square meters.

This document relates to oxidative dehydrogenation catalyst materials that include molybdenum, vanadium, beryllium, oxygen, and optionally aluminum.

Described is a process for the production of a zeolitic material having an MFI, MEL, and/or MWW-type framework structure comprising YO.sub.2 and X.sub.2O.sub.3. The process comprises (1) preparing a mixture comprising one or more sources for YO.sub.2, one or more sources for X.sub.2O.sub.3, and one or more solvents; (2) crystallizing the mixture obtained in step (1) to obtain a zeolitic material having an MFI, MEL and/or MWW-type framework structure; and (3) impregnating the zeolitic material obtained in step (2) with one or more elements selected from the group of alkaline earth metals. Y is a tetravalent element, and X is a trivalent element. The mixture crystallized in step (2) contains 3 wt.-% or less of one or more elements M based on 100 wt-% of YO.sub.2, wherein M stands for sodium.

A process for the production of C.sub.4 olefins, which may include: contacting a hydrocarbon mixture comprising alpha-pentenes with an isomerization catalyst to form an isomerization product comprising beta-pentenes; contacting ethylene and the beta-pentenes with a first metathesis catalyst to form a first metathesis product comprising butenes and propylene, as well as any unreacted ethylene and C.sub.5 olefins; and fractionating the first metathesis product to for an ethylene fraction, a propylene fraction, a butene fraction, and a C.sub.5 fraction.

The present invention relates to a catalyst for the dehydrogenation of hydrocarbons which is based on iron oxide and a process for producing it. The catalyst comprises at least one iron compound, at least one potassium compound and from 11 to 24% by weight of at least one cerium compound, calculated as CeO.sub.2, wherein the at least one iron compound and the at least one potassium compound are at least partly present in the form of one or more K/Fe mixed oxide phases of the general formula K.sub.xFe.sub.yO.sub.z, where x is from 1 to 17; y is from 1 to 22 and z is from 2 to 34, and comprises at least 50% by weight, based on the total catalyst, of the K/Fe mixed oxide phases, and also a process for producing it.

The invention has objects of providing an olefin production method which can produce an olefin with high efficiency by the dehydration reaction of an alcohol even in the presence of a ketone without the occurrence of side reactions such as the Aldol condensation of the ketone, as well as providing an olefin production method which can produce an olefin with high activity and high selectivity in a single reaction step by directly reacting a corresponding ketone and hydrogen. The former olefin production method of the invention produces an olefin from an alcohol using a silica gel (A) as a dehydration catalyst which is obtained by bringing a silica gel (X) prepared from an alkyl orthosilicate into contact with a water-soluble aluminum compound and calcining the contact product or is obtained from a wet-process silica gel (Y) prepared from an alkali silicate and which contains an aluminum compound at 10 to 1000 ppm in terms of aluminum element as well as an alkali metal and an alkaline earth metal at a total of 0 to 350 ppm. The latter olefin production method produces an olefin from a ketone and hydrogen in a single reaction step in the presence of the silica gel (A) and a silver-containing inorganic substance (B).

The present invention discloses a process to treat a ferrite based catalyst useful in the oxidative dehydrogenation of monololefins and diolefins which process includes a preheat step prior to use of the catalyst in the OXO-D reactor. The catalyst is preferably a zinc ferrite catalyst for the production of butadiene. It has been observed that substantially no nitrogen oxide emissions result from the use of this treated catalyst in the reactor unit during the oxidative dehydrogenation reaction.

The present disclosure provides a catalyst for oxidative dehydrogenation of butene to butadiene, comprising at least one compound of formula Zn.sub.aAl.sub.bM.sub.cFe.sub.eO.sub.f.Z(-Fe.sub.2O.sub.3), wherein M is at least one element chosen from Be, Mg, Ca, Sr, Mn, Ba, Cu, Co, and Ni, Z represents the percentage by weight of -Fe2O3 in the catalyst and ranges from 10% to 70%. Also provided herein is a process of preparing said catalyst and the use of said catalyst in an oxidative dehydrogenation of butene to butadiene processes.