B01J2229/16

Method for manufacturing modified aluminosilicate, modified aluminosilicate, and method for manufacturing aromatic dihydroxy compound using the same

The method for manufacturing a modified aluminosilicate includes a first step of treating an aluminosilicate with an acid, a second step of primarily calcining the treated material obtained in the first step at 550° C. to 850° C., and a third step of contacting the calcined material obtained in the second step with a liquid containing one or more Group 4 elements and/or Group 5 elements, and then drying and secondarily calcining the resultant. The modified aluminosilicate includes one or more Group 4 elements and/or Group 5 elements, and exhibits an absorbance at 300 nm in an ultraviolet visible spectrum of 1.0 or higher. The method for manufacturing aromatic dihydroxy compounds includes reacting a phenol with hydrogen peroxide in the presence of a specific modified aluminosilicate.

CATALYTIC CRACKING OF GLYCERIDE OILS WITH DEACTIVATED PHOSPHORUS-CONTAINING ZSM-5 LIGHT OLEFINS ADDITIVES
20230137243 · 2023-05-04 ·

A process is provided for the catalytic cracking of a glyceride oil feedstock with a catalyst composition containing a deactivated phosphorus-containing ZSM-5 light olefins selective additive.

DESILICATED SMALL CRYSTAL ZSM-5 AND METHOD OF MAKING THE SAME
20230365420 · 2023-11-16 ·

A desilicated crystalline material having an MFI (ZSM-5) framework type, a molar silica to alumina ratio (SAR) of 15 or more, and mean crystal size of about 200 nm or less, is disclosed. The disclosed crystalline material has a mesopore volume of at least 0.40 cm.sup.3/g and a micropore volume of at least 0.10 cm.sup.3/g. A method of preparing a desilicated crystalline material is also disclosed. The method comprises mixing a starting ZSM-5 material having a mean crystal size of 200 nm or less in a base solution, collecting the solids by filtration or other separation methods, drying, and optionally calcining the solids.

METHODS OF ETHERIFICATION

Embodiments of the present disclosure are directed towards methods of etherification including modifying a zeolite catalyst with silica to provide a silica modified zeolite catalyst; and contacting the silica modified zeolite catalyst with an olefin and an alcohol to produce a monoalkyl ether.

HYDROPHOBIC ZEOLITE, METHOD FOR PRODUCING SAME AND USE OF SAME
20220259054 · 2022-08-18 ·

A hydrophobic zeolite which has a water adsorption of (6 g/100 g zeolite) or less at 25° C. at RH 60% and a toluene adsorption of (9 g/100 g zeolite) or more at 25° C. under 0.01 kPa.

METHOD FOR PRODUCING ZEOLITE

A method for producing a zeolite with improved Si/Al according to the present invention includes the steps of: subjecting a zeolite synthesized without using an organic structure directing agent to ion exchange, thereby obtaining a sodium-type, a proton-type, or an ammonium-type zeolite; and bringing the zeolite subjected to ion exchange into contact with an ammonium salt solution, thereby dealuminating the zeolite. It is preferable that the ammonium salt is any one of ammonium oxalate, ammonium fluoride, ammonium fluorosilicate, ammonium fluoroborate, ammonium fluorophosphate, ammonium fluorotitanate, and ammonium florozirconate. It is also preferable that the zeolite after ion exchange is exposed to water vapor, and is then brought into contact with the ammonium salt solution.

Three stage catalytic process for pyrolysis oil upgrading to xylenes

A method for upgrading pyrolysis oil includes contacting a pyrolysis oil feed with hydrogen in the presence of a mixed metal oxide catalyst in a slurry reactor to produce an intermediate stream comprising light aromatic compounds comprising mono-aromatic compounds, di-aromatic compounds, or both, passing the intermediate stream to a hydrocracking reactor, contacting the intermediate stream with hydrogen in the presence of a hydrocracking catalyst in a hydrocracking reactor to produce a hydrocracking effluent comprising aromatic compounds having six to nine carbon atoms, passing the hydrocracking effluent to a transalkylation reactor, and contacting the hydrocracking effluent with hydrogen in the presence of a transalkylation catalyst in the transalkylation reactor to produce a transalkylation effluent comprising xylenes.

Fluid catalytic cracking (FCC) process and apparatus for production of light olefins

The instant disclosure provides a composition for fluid catalytic cracking of petroleum based feedstock into useful short chain olefins. The composition comprising: 76-86% of a non-zeolitic material; and 2-30% of at least one zeolite material, the percentage being based on weight of the catalyst composition, wherein one of the zeolites has been modified with 0.1-2.5 wt % metal. The said catalyst was found to be selective in enhancing the usable propylene gas content, while reducing the undesirable dry gas content of the cracked olefinic products. The present disclosure also provides a process for the preparation of the composition. The present disclosure also provides an apparatus (100) and process (200) for fluid catalytic cracking to obtain light olefins. The apparatus comprises a second riser (33) that includes a lower dense riser (2) and upper dilute riser (3). Further, the lower dense riser (2) has a diameter that is 1.1 to 2 times that of the upper dilute riser (3).

MOLECULAR SIEVE CATALYST, PREPARATION METHOD THEREFOR, AND APPLICATION THEREOF

Provided are a molecular sieve catalyst, a preparation method therefor, an application thereof. The molecular sieve catalyst contains a modified Na-MOR molecular sieve, and the modification comprises: organic ammonium salt exchange, dealumination treatment, and ammonium ion exchange. The catalyst obtained by the method is used in dimethyl ether for one-step production of methyl acetate. The catalyst has high activity and stable performance, and the needs of industrial production can be satisfied.

Manufacturing hydrocracking catalyst

A method including subjecting an ultra-stable Y-type zeolite having a low silica-to-alumina molar ratio (SAR), such as in a range of 3 to 6, to acid treatment and heteroatom incorporation contemporaneously to give a framework-modified ultra-stable Y-type zeolite.