Embodiments of catalyst systems and methods of synthesizing catalyst systems are provided. The catalyst system may include a core comprising a zeolite; and a shell comprising a microporous fibrous silica. The shell may be in direct contact with at least a majority of an outer surface of the core. The catalyst system may have a Si/Al molar ratio greater than 5. At least a portion of the shell may have a thickness of from 50 nanometers (nm) to 360 nm.

Embodiments of the present disclosure relate to zeolites and method for making such zeolites. According to embodiments disclosed herein, a zeolite may have a microporous framework including a plurality of micropores having diameters of less than or equal to 2 nm and a plurality of mesopores having diameters of greater than 2 nm and less than or equal to 50 nm. The microporous framework may include an MFI framework type. The microporous framework may include silicon atoms, aluminum atoms, oxygen atoms, and transition metal atoms. The transition metal atoms may be dispersed throughout the entire microporous framework.

Solid porous composite ZSM-5 materials comprising a generally vertical orientation of an array of pentacil-zeolite crystals on a porous substrate.

A process for upgrading a hydrocarbon feed includes contacting the hydrocarbon feed with steam in the presence of a cracking catalyst at reaction conditions sufficient to cause at least a portion of hydrocarbons in the hydrocarbon feed to undergo one or more cracking reactions to produce a steam catalytic cracking effluent comprising light olefins, light aromatic compounds, or both. The cracking catalyst is hierarchical mesoporous ZSM-5 zeolite. The hierarchical mesoporous ZSM-5 zeolite is made by providing a starting ZSM-5 zeolite, disintegrating the a portion of the starting ZSM-5 in the presence of a surfactant using sodium hydroxide, and then recrystallizing the zeolite constituents in the presence of the surfactant to produce recrystallized ZSM-5 zeolite. The recrystallized ZSM-5 zeolite is then recovered and calcined to produce the hierarchical mesoporous ZSM-5 zeolite.

The present invention is in the field of processes for the production of BioLPG, and catalysts for use in said processes.

The present invention relates to a method using a specific catalyst for upgrading ketoacid to intermediates for fuel and chemical industry, intermediates obtained by the method and to their use.

Methods of forming mesoporous zeolites with tunable pore widths are provided. In some embodiments, the method includes mixing a silicon-containing material, an aluminum-containing material, and at least a quaternary amine to produce a zeolite precursor solution. The zeolite precursor solution is pre-crystallized at a pre-crystallization temperature of greater than 125 C. and autogenous pressure to form a pre-crystallized zeolite precursor solution and combined with two or more distinct organosilane mesopore templates to produce a zeolite precursor gel. The zeolite precursor gel is crystallized to produce a crystalline zeolite intermediate and the crystalline zeolite intermediate is calcined to produce the mesoporous zeolite.

Catalysts and methods for use in conversion of glycerides and free fatty acids to biodiesel are described. A batch or continuous process may be used with the catalysts for transesterification of triglycerides with an alkyl alcohol to produce corresponding mono carboxylic acid esters and glycerol in high yields and purity. Similarly, alkyl and aryl carboxylic acids and free fatty acids are also converted to corresponding alkyl esters. Catalysts are capable of simultaneous esterification and transesterification under same process conditions. The described catalysts are thermostable, long lasting, and highly active.

A rare earth- and phosphorus-containing molecular sieve of MFI structure rich in mesopores has a ratio of n(SiO.sub.2)/n(Al.sub.2O.sub.3) of more than 15 and less than 70. The molecular sieve has a content of phosphorus of 1-15 wt %, calculated as P.sub.2O.sub.5 and based on the dry weight of the molecular sieve. The content of the supported metal in the molecular sieve is 1-10 wt % supported metal M1 and 0.1-5 wt % supported metal M2 based on the oxide of the supported metal and the dry weight of the molecular sieve. The supported metal M1 is one or two selected from lanthanum and cerium, and the supported metal M2 is one selected from iron, cobalt, nickel, copper, manganese, zinc, tin, bismuth and gallium; the volume of mesopores in the molecular sieve represents 40-70% by volume of the total pore volume of the molecular sieve by volume.

The present invention relates to a process for producing aromatics, a process for producing p-xylene and terephthalic acid, and a device for producing aromatics. The process for producing aromatics at least comprises a step of producing C8 olefin from a compound having a lactone group and a step of producing aromatics from the C8 olefin. The process for producing aromatics has the characters of high yield of aromatics and high selectivity to xylene.