The process comprises hydrocracking a hydrocarbon feed in a single stage. The catalyst comprises a base impregnated with metals from Group 6 and Groups 8 through 10 of the Periodic Table. The base of the catalyst used in the present hydrocracking process comprises alumina, an amorphous silica-alumina (ASA) material, a USY zeolite, optionally a beta zeolite, and zeolite ZSM-12.

A catalyst based on a zeolite of AFX structural type and on at least one transition metal, can be prepared by a process comprising at least the following steps: i) mixing, in an aqueous medium, of at least one source of silicon in oxide form SiO2, of at least one source of aluminium in oxide form Al2O3, of an organic nitrogen-comprising compound R, of at least one source of at least one alkali metal and/or alkaline-earth metal M until a homogeneous precursor gel is obtained; ii) hydrothermal treatment of said precursor gel to obtain a crystallized solid phase, iii) at least one ion exchange with a transition metal; iv) heat treatment. The catalyst can be used for the selective reduction of NOx employing the catalyst, and can achieve an NOx conversion (conversion=(NOx inletNOx outlet)/NOx inlet) of 100% at a temperature of 430 C. or lower.

Provided is a structured catalyst for hydrodesulfurization that suppresses the decline in catalytic activity and achieves efficient hydrodesulfurization. The structured catalyst for hydrodesulfurization (1) includes a support (10) of a porous structure composed of a zeolite-type compound, and at least one catalytic substance (20) present in the support (10), the support (10) having channels (11) connecting with each other, and the catalytic substance (20) being present at least in the channels (11) of the support (10).

An AFX framework type zeolite having a SiO.sub.2/Al.sub.2O.sub.3 molar ratio of greater than 50 is disclosed. The high-silica AFX framework type zeolite is synthesized from a reaction mixture having high silica and low hydroxide concentrations in the presence of an organic structure directing agent comprising 1,3-bis(1-adamantyl)imidazolium cations.

One object is to provide an aldehyde decomposition catalyst, and an exhaust gas treatment apparatus and an exhaust gas treatment method using the aldehyde decomposition catalyst that achieve low cost and sufficient aldehyde decomposition performance with a small amount of the catalyst. An aldehyde decomposition catalyst of the present invention is made of a zeolite in a cation form NH.sub.4 having a structure selected from MFI and BEA and carrying at least one metal selected from the group consisting of Cu, Mn, Ce, Zn, Fe, and Zr.

One object is to provide an aldehyde decomposition catalyst, and an exhaust gas treatment apparatus and an exhaust gas treatment method using the aldehyde decomposition catalyst that achieve low cost and sufficient aldehyde decomposition performance with a small amount of the catalyst. An aldehyde decomposition catalyst of the present invention is made of a zeolite in a cation form NH.sub.4 having a structure selected from MFI and BEA and carrying at least one metal selected from the group consisting of Cu, Mn, Ce, Zn, Fe, and Zr.

The present invention relates to the synthesis of molecular sieves of the STT and ITE framework types using, as structure directing agent Q, [L(DETA)2].sup.2+ cation or [L(TEPA)].sup.2+ cation, or a mixture thereof, where L is a divalent metal cation comprising at least one of Ni, Co and Mn and DETA is diethylene triamine and TEPA is tetraethylene pentamine.

The present invention relates to the synthesis of molecular sieves of the STT and ITE framework types using, as structure directing agent Q, [L(DETA)2].sup.2+ cation or [L(TEPA)].sup.2+ cation, or a mixture thereof, where L is a divalent metal cation comprising at least one of Ni, Co and Mn and DETA is diethylene triamine and TEPA is tetraethylene pentamine.

Methods and systems for production of consistently-sized BEA zeolite nano-crystals incorporating at least one metal oxide, the method including removing an organic template from a BEA zeolite comprising an organic template via calcination; desilicating the BEA zeolite following the step of removing the organic template; incorporating at least one metal oxide into the structure of the BEA zeolite after the step of desilicating; protonating the BEA zeolite after the step of incorporating the at least one metal oxide; and calcining the BEA zeolite after the step of protonating to form a modified BEA zeolite product.

The present invention relates to a catalyst system for olefin metathesis, the catalyst system comprising: a) a first system zone substantially comprising a layered double hydroxide; and b) a second system zone comprising a metathesis catalyst.