Engelhard Corporation

Basf Corporation

John M Macaoay

David M Stockwell

Paul R Suitch

Michel Deeba

Gerald Steven Koermer

Rostam Jai Madon

Mingting Xu

Roland Von Ballmoos

Eric W Stern

A cracking catalyst contains a substantially inert core and an active shell, the active shell containing a zeolite catalyst and a matrix. Methods of making and using the cracking catalyst are also described.

Structurally enhanced cracking catalysts

A cracking catalyst contains a substantially inert core and an active shell, the active shell containing a zeolite catalyst and a matrix. The catalyst is formed by spray-drying a slurry containing water, substantially inert microspheres and a zeolite precursor and crystallizing zeolite in the active shell to create the cracking catalyst. Methods of using the cracking catalyst are also described.

A novel method of forming ZSM-5 comprises reacting calcined kaolin microspheres with silicate and a seed solution used for forming zeolite Y under conditions of pH, temperature, and time to yield ZSM-5 crystals formed in-situ on said calcined kaolin microspheres. The reaction medium does not contain any organic templates or ZSM-5 seeding crystals.

In-situ ZSM-5 synthesis

A calcined cracking catalyst comprising zeolite crystals in an inorganic oxide matrix and containing less than about 0.75% Na.sub.2 O and, from 0.1 to 10% P expressed as P.sub.2 O.sub.5, the cracking catalyst being further characterized by exhibiting a spectra with a peak at about 3735 cm.sup.-1 when treated with pyridine and analyzed by FTIR. A process for manufacturing an FCC catalyst characterized by high tolerance to contaminated metals comprises providing fluid cracking catalyst microspheres containing zeolite Y in an inorganic oxide matrix and analyzing 20 to 60% by weight Al.sub.2 O.sub.3 and analyzing less than 0.75% wt. Na.sub.2 O; impregnating the catalyst with a solution of a phosphate or phosphite salt in amount such the microspheres analyze 0.5 to 10% by weight P.sub.2 O.sub.5 and calcining the microspheres in the absence of steam at a temperature above 1300.degree. F. and below 1600.degree. F. and recovering the product characterized exhibiting a spectra with a peak at about 3687 cm.sup.-1 and the intensity ratio of the peak at 3687 cm-.sup.1 to the peak at 3675 cm-.sup.1 is greater than about 0.8 when treated with pyridine and analyzed by FTIR.

Catalyst for cracking oil feedstocks contaminated with metal

This invention relates to microspheres produced by spray drying clay slurries and calcining the product to form attrition resistant microspheres. Phosphoric acid is injected in a neutral to mildly alkaline dispersed high solids kaolin slurry immediately before spray drying to improve properties of the microspheres.

Phosphorus bound porous microspheres

An in situ process for making improved zeolitic fluid cracking catalyst by spray drying a mixture of hydrous kaolin and spinel, essentially free from metakaolin, calcining the resulting microspheres to convert the hydrous kaolin to metakaolin, and reacting microspheres composed of a mixture of spinel and metakaolin forms of calcined clay with a seeded alkaline sodium silicate solution. The weight percent of hydrous kaolin in the starting (uncalcined) microspheres is greater than the spinel content.

Modified microsphere FCC catalysts

Disclosed is a vanadium trap for use in FCC which comprises a major amount of calcined kaolin clay, free magnesium oxide and an in situ formed magnesium silicate cement binder. Also disclosed are procedures for the preparation of the trap by forming a slurry in water of hydrous kaolin clay, magnesium oxide or magnesium hydroxide and sodium silicate, aging the slurry to form magnesium silicate in situ, optionally adding additional kaolin, colloidal silica or both, spray drying, and calcining the resulting spray dried microspheres without forming appreciable amounts of crystalline magnesium silicates or crystalline magnesium aluminates.

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Linden, NJ, United States of America

John M Macaoay