A method for reducing the level of occluded alkali metal cations from an MSE-framework type molecular sieve comprises either (a) contacting the molecular sieve with a solution containing ammonium ions at a temperature of at least about 50 C. to ammonium-exchange at least part of the occluded potassium ions or (b) contacting the molecular sieve with steam at a temperature of at least about 300 C. and then subjecting the steamed molecular sieve to ammonium exchange.

A method for producing double-component modified molecular sieve comprises adding molecular sieve to an aqueous solution containing phosphorus to form a mixture, allowing the mixture to react at pH of 1-10, temperature of 70-200 C. and pressure of 0.2-1.2 MPa for 10-200 min, and then filtering, drying and baking the resultant to obtain phosphorus-modified molecular sieve, and then adding the phosphorus-modified molecular sieve to an aqueous solution containing silver ions, allowing the phosphorus-modified molecular sieve to react with silver ions at 0-100 C. in dark condition for 30-150 min, and then filtering, drying and baking. The obtained double-component modified molecular sieve contains 88-99 wt % molecular sieve with a ratio of silica to alumina between 15 and 60, 0.5-10 wt % phosphorus (based on oxides) and 0.01-2 wt % silver (based on oxides), all based on dry matter. A catalyst produced from the double-component modified molecular sieve has improved hydrothermal stability and microactivity.

The present invention relates to a monolith catalyst for reforming reaction, and more particularly, to a thermally stable (i.e. thermal resistance-improved) monolith catalyst for reforming reaction having a novel construction such that any one of Group 1A to Group 5A metals are used as a barrier component in the existing catalyst particles to inhibit carbon deposition occurring during the reforming reaction in a process for formation of a reforming monolith catalyst while improving thermal durability as well as non-activation of the catalyst due to a degradation.

Described are catalyst materials and catalytic articles comprising a metal exchanged SAPO material comprising a plurality of substitutional sites consisting essentially of Si(4Al) sites and substantially free of Si(0Al) sites. The materials and catalytic articles are useful in methods and systems to catalyze the reduction of nitrogen oxides in the presence of a reductant.

Disclosed herein is a catalyst component suitable for petroleum refining applications (e.g., fluid catalytic cracking and hydrocracking) that includes a MSB zeolite structure (e.g., MCM-68) and a non-zeolitic matrix. The first component may be combined with additional components into a catalyst composition. Also disclosed herein are methods of preparing the catalyst component and/or catalyst compositions as well as method of using the catalyst component and/or catalyst composition.

A new crystalline molecular sieve designated SSZ-95 is disclosed. In general, SSZ-95 is synthesized from a reaction mixture suitable for synthesizing MTT-type molecular sieves and maintaining the mixture under crystallization conditions sufficient to form product. The product molecular sieve is subjected to a pre-calcination step, and ion-exchange to remove extra-framework cations, and a post-calcination step. The molecular sieve has a MTT-type framework and a H-D exchangeable acid site density of 0 to 50% relative to molecular sieve SSZ-32.

Embodiments of the invention provide a method for the fluid catalytic cracking of a heavy hydrocarbon feedstock. According to at least one embodiment, the method includes supplying the heavy hydrocarbon feedstock to a reaction zone having a catalyst, such that both the heavy hydrocarbon feedstock and the catalyst are in contact in a down-flow mode, wherein said contact between the heavy hydrocarbon feedstock and the catalyst takes place in a fluidized catalytic cracking apparatus having a separation zone, a stripping zone, and a regeneration zone. The method further includes maintaining the reaction zone at a temperature of between 500 and 600 C., such that the hydrocarbon feedstock converts into a cracked hydrocarbon effluent comprising light olefins, gasoline, and diesel. The catalyst includes between 10 and 20% by weight of a phosphorous modified sub-micron ZSM-5, between 10 and 20% by weight of an ultra-stable Y-type zeolite, between 20 and 30% by weight of a pseudoboehmite alumina, and between 20 and 40% by weight of kaolin. The phosphorous modified sub-micron ZSM-5 has an average crystal size between 50 and 400 nm, inclusive, and a silica to alumina ratio of 1:2 to 1:4, inclusive.

A new crystalline molecular sieve designated SSZ-95 is disclosed. In general, SSZ-95 is synthesized from a reaction mixture suitable for synthesizing MTT-type molecular sieves and maintaining the mixture under crystallization conditions sufficient to form product. The product molecular sieve is subjected to a pre-calcination step, and ion-exchange to remove extra-framework cations, and a post-calcination step. The molecular sieve has a MTT-type framework and a H-D exchangeable acid site density of 0 to 50% relative to molecular sieve SSZ-32.

Disclosed herein are phosphated zeolites and methods of formation and stabilization thereof. In at least one embodiment, a phosphated zeolite is formed by performing one or more acid treatments on a zeolite using a phosphorus source, and subsequently increasing the reaction pH under conditions sufficient to induce condensation of phosphorus onto the zeolite and re-insertion of the extracted framework aluminum onto the zeolite.

A catalytic cracking agent has an active component consisting of a phosphorus-modified molecular sieve and a non-phosphorus-modified molecular sieve or only consisting of a phosphorus-modified molecular sieve. According to an electron probe microanalysis (EPMA), the D value of phosphorus in the catalytic cracking agent is 65%, preferably 68%, provided that the active component consists of the phosphorus-modified molecular sieve and the non-phosphorus-modified molecular sieve, or the D value of phosphorus in the catalytic cracking agent is 82%, preferably 84%, provided that the active component only consists of the phosphorus-modified molecular sieve.