A method is disclosed for synthesizing MTW framework type zeolites via interzeolite transformation in the presence of polyethyleneimine.

A method is disclosed for synthesizing MTW framework type molecular sieves using 1,1-diethyl-4-methylpiperidinium cations as a structure directing agent.

Catalysts and corresponding methods for oligomerization of olefins to distillate boiling range compounds are provided. The oligomerization can be performed in the presence of a catalyst including a 10-member ring or 1-D 12-member ring zeolitic framework material that contains both silica and alumina. The zeolitic framework material can have a low molar ratio of silica to alumina. The zeolitic framework material can be ion-exchanged to a small but substantial degree with alkaline earth metal cations, such as Mg, Ca, Sr, or Ba. The small but substantial amount of ion exchange can correspond to having a molar ratio of alkaline earth metal to aluminum of up to 0.2.

Disclosed is a process and apparatus for switching oligomerization feed between a first oligomerization zone that includes a uni-dimensional small pore zeolite to make more diesel and a second oligomerization zone that includes SPA catalyst for making more gasoline. The diesel can be recycled to make more propylene. The process and apparatus will provide refiners with flexibility to produce the most valuable product commensurate with fluctuating market conditions.

The present disclosure relates to a preparing method of a zeolite core/silica zeolite shell composite, which includes adding a zeolite seed crystal into a gel solution containing a silicon-source compound, a structure directing agent and a fluorine anion-source compound, and then, crystallizing the gel solution for growing a silica zeolite shell containing a crystal structure which is coherent with that of the zeolite seed crystal; a zeolite core/silica zeolite shell composite prepared by the preparing method above; and catalytic use of the zeolite core/silica zeolite shell composite.

A catalyst for the dehydroaromatization of lower alkanes comprising boron in an amount of less than 1 wt % is supported on an inorganic support. The catalyst is useful in the production of aromatics from lower alkanes.

The present disclosure relates to a naphtha reforming process for obtaining reformed naphtha comprising contacting naphtha with a catalyst, the catalyst comprising a chloride free zeolite coated alumina support impregnated with 0.01 wt % to 0.5 wt % active metal and 0.01 wt % to 0.5 wt % promoter metal, wherein the thickness of the zeolite coating on the alumina support ranges from 100 m to 200 m, which results in formation of reformed products of naphtha and ethylbenzene formed in-situ.

A family of new crystalline molecular sieves designated SSZ-91 is disclosed. 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.

Methods for introducing mesoporosity into zeolite materials that employ an acid pretreatment step are provided. By utilizing a non-acidic chelating agent during the acid treatment step, the zeolite material can be pretreated with a strong acid, often in higher concentrations or over shorter contact times, than had previously been contemplated. The resulting acid-treated mesoporous materials retain desirable properties, including Si/Al, UCS, and total mesopore and micropore volume. The ability to use a stronger acid without damaging the zeolite material results in a less expensive process capable of producing mesoporous zeolite materials suitable for a wide range of uses.

Processes and systems for converting an oxygenate feedstock to a hydrocarbon product, selectivated catalysts and processes for reducing off-spec gasoline production during start-up are provided herein.