A catalyst containing a IZM-2 zeolite and a specific content of alkali metal or alkaline-earth metal compounds, and a process for the isomerization of an aromatic C8 cut using the catalyst.

A hydrogenolysis bimetallic supported catalyst comprising a first metal, a second metal, and a zeolitic support; wherein the first metal and the second metal are different; and wherein the first metal and the second metal can each independently be selected from the group consisting of iridium (Ir), platinum (Pt), rhodium (Rh), ruthenium (Ru), palladium (Pd), molybdenum (Mo), tungsten (W), nickel (Ni), and cobalt (Co).

Molecular sieves comprising intergrowths of cha and aft having an “sfw-GME tail”, at least one structure directing agent (SDA) within the framework of the molecular sieve, an intergrowth of CHA and GME framework structures, cha cavities, and aft cavities are described. A first SDA comprising either an N,N-dimethyl-3,5-dimethylpiperidinium cation or a N,N-diethyl-2,6-dimethylpiperidinium cation is required. A second SDA, which can further be present, is a CHA or an SFW generating cation. The amount of the second SDA-2 used can change the proportion of the components in the cha-aft-“sfw-GME tail”. Activated molecular sieves formed from SDA containing molecular sieves are also described. Compositions for preparing these molecular sieves are described. Methods of preparing a SDA containing JMZ-11, an activated JMZ-11, and metal containing activated JMZ-11 are described. Methods of using activated JMZ-11 and metal containing activated JMZ-11 in a variety of processes, such as treating exhaust gases and converting methanol to olefins are described.

The invention relates to a catalyst system and process for preparing dimethyl ether from synthesis gas as well as the use of the catalyst system in this process.

Molecular sieves comprising intergrowths of cha and aft having an “sfw-GME tail”, at least one structure directing agent (SDA) within the framework of the molecular sieve, an intergrowth of CHA and GME framework structures, cha cavities, and aft cavities are described. A first SDA comprising either an N,N-dimethyl-3,5-dimethylpiperidinium cation or a N,N-diethyl-2,6-dimethylpiperidinium cation is required. A second SDA, which can further be present, is a CHA or an SFW generating cation. The amount of the second SDA-2 used can change the proportion of the components in the cha-aft-“sfw-GME tail”. Activated molecular sieves formed from SDA containing molecular sieves are also described. Compositions for preparing these molecular sieves are described. Methods of preparing a SDA containing JMZ-11, an activated JMZ-11, and metal containing activated JMZ-11 are described. Methods of using activated JMZ-11 and metal containing activated JMZ-11 in a variety of processes, such as treating exhaust gases and converting methanol to olefins are described.

Catalytic compositions and sequential catalytic methods are generally described. in some embodiments, a composition comprises a first catalyst comprising a Cu-modified zeolite, and a second catalyst capable of a coupling reaction between (a) an intermediate resulting from a reaction of a reactant at the first catalyst, and (b) a co-reagent, wherein a rate of diffusion of the co-reagent within one or more cages and/or pores of the first catalyst is lower than a rate of diffusion of the intermediate within the one or more cages and/or pores of the first catalyst.

A family of new crystalline molecular sieves designated SSZ-91 is disclosed, as are methods for making SSZ-91 and uses for SSZ-91. Molecular sieve SSZ-91 is structurally similar to sieves falling within the ZSM-48 family of molecular sieves, and is characterized as: (1) having a low degree of faulting, (2) a low aspect ratio that inhibits hydrocracking as compared to conventional ZSM-48 materials having an aspect ratio of greater than 8, and (3) is substantially phase pure.

A metal-zeolite composition comprising: (i) a zeolite phase; and (ii) a metal, other than aluminum or silicon, nanoscopically dispersed throughout said zeolite phase, wherein, if agglomerations of said metal are present, the agglomerations have a size of no more than 1 micron, wherein the zeolite may be, for example, a dealuminated zeolite, and the metal may be selected from transition metals, main group metals, and lanthanide metals. Also described herein is a method for producing the metal-zeolite composition in which a zeolite phase and metal salt are mixed and ground by a solvent-less ball milling process to produce an initial mixture, and calcining the initial mixture to produce the metal-zeolite composition. Further described herein is a method for converting an oxygen-containing organic species to a hydrocarbon, the method comprising contacting the species with the above described metal-loaded zeolite catalyst at a temperature of at least 100° C. and up to 550° C.

The present invention relates to a method for the oligomerization of ethylene, and more specifically, to a method for the preparation of mainly ethylene oligomers of C.sub.10 or higher, which comprises obtaining mainly ethylene oligomers of C.sub.4 or higher by performing a first oligomerization of an ethylene gas using a Ni-containing mesoporous catalyst, followed by a second oligomerization using an ion exchange resin, etc. The method for the preparation of ethylene oligomers according to the present invention can produce C.sub.8-16 ethylene oligomers in high yield without inducing inactivation of a catalyst, compared to the conventional technology of ethylene oligomerization by a one-step process.

The invention relates to a catalyst and catalyst layer and process for preparing dimethyl ether from synthesis gas or methanol as well as the use of the catalyst or catalyst layer in this process.