Abstract: Provided is an improved process for olefin oligomerization allowing one to realize superior selectivity. The process comprises contacting a hydrocarbon feed comprised of straight and branched chain olefins under oligomerization conditions with a catalyst comprising delaminated SSZ-70. The delaminated SSZ-70 offers a zeolite layer with a single unit cell of thickness in one dimension, allowing for elimination of mass transfer in comparison with regular SSZ-70. The result is superior selectivity.

Abstract: Crystalline molecular sieves and their synthesis using quaternary N-methyl-diisoalkylammonium cations as organic structure directing agents are disclosed. The structure directing agent has the following structure (1): in which R1 is selected from hydrogen, a methyl group, an ethyl group, a propyl group, and a hydroxymethyl group; and R2, R3, R4 and R5 are independently selected from a methyl group, an ethyl group, and a propyl group.

Abstract: Provided is an improved hydroprocessing process allowing one to realize superior isoselectivity. The process comprises contacting a feed comprised of normal hydrocarbons under hydroprocessing conditions with a catalyst comprising delaminated SSZ-70. The delaminated SSZ-70 has been found to provide unexpected improvements in the catalysis of hydroprocessing hydrocarbons. Delaminated SSZ-70 offers a zeolite layer with a single unit cell of thickness in one dimension, allowing an elimination of mass transfer in comparison with non-delaminated SSZ-70.

Abstract: Uses are disclosed for a new crystalline molecular sieve designated SSZ-102 synthesized using an N,N?-dimethyl-1,4-diazabicyclo[2.2.2]octane dication as a structure directing agent. SSZ-102 has ESV framework topology.

Abstract: The present invention is directed to the synthesis of novel delaminated layered zeolite precursor materials prepared by fluoride/chloride anion-promoted exfoliation. The method comprises, for example, using a combination of fluoride and chloride anions at a mild pH in aqueous solution to affect delamination of a layered zeolite precursor. The method can also comprise using a combination of fluoride and chloride anions in a non-aqueous solution comprising an organic solvent. The method may be used in conjunction with either acidification or sonication, or both. The resulting delaminated zeolite precursors are then isolated. Precursors that are then isolated lack amorphous silica content. The UCB-1 product is an example of such a novel oxide material and is obtained in yields in excess of 90% without the need for sonication.

Abstract: The present invention is directed to an alumino-borosilicate SSZ-57 zeolite having enhanced large pore selectivity. The alumino-borosilicate SSZ-57 zeolite of the present invention is characterized as having substantially all of its aluminum atoms located within regions of the zeolite structure which form the 12 ring channels.

Abstract: The present invention is directed to the synthesis of novel delaminated layered zeolite precursor materials prepared by fluoride/chloride anion-promoted exfoliation. The method comprises, for example, using a combination of fluoride and chloride anions at a mild pH in a non-aqueous solution to affect delamination of a layered zeolite precursor, generally comprising an organic solvent. The method may be used in conjunction with either acidification or sonication, or both. The resulting delaminated zeolite precursors are then isolated. Precursors that are then isolated lack amorphous silica content. The UCB-1 product is an example of such a novel oxide material and is obtained in yields in excess of 90% without the need for sonication.

Abstract: A method is disclosed for preparing pure phase aluminosilicate molecular sieves having the CHA framework type using a trimethylphenylammonium cation as a structure directing agent.

Abstract: Uses for a new crystalline molecular sieve designated SSZ-98 are disclosed. SSZ-98 has the ERI framework type and is synthesized using a N,N?-dimethyl-1,4-diazabicyclo[2.2.2]octane dication as a structure directing agent.

Abstract: A new crystalline zinc (silico)aluminophosphate molecular sieve designated SSZ-90 is disclosed. SSZ-90 is isostructural with the DFO framework type and is synthesized using an ionic liquid as both the solvent and the structure directing agent. The ionic liquid [Q+A?] comprises a cation (Q+) selected from the group consisting of 1,3-diisopropylimidazolium, 1,3-diisobutylimidazolium, and 1-isopropyl-3-isobutylimidazolium and an anion (A?) which is not detrimental to the formation of the molecular sieve.

Abstract: Provided is a process of conducting a Baeyer-Villiger oxidation which comprises contacting a ketone and an oxidant in the presence of an Sn-DZ-1 catalyst to thereby oxidize the ketone to an ester. The Sn-DZ-1 catalyst comprises Sn heteroatoms on the external surface of the zeolitic material lattice framework, and B heteroatoms, or silanols created from boron hydrolysis, throughout the remainder of the lattice framework.

Abstract: 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.

Abstract: A new crystalline zinc (silico)aluminophosphate molecular sieve designated SSZ-90 is disclosed. SSZ-90 is isostructural with the DFO framework type and is synthesized using an ionic liquid as both the solvent and the structure directing agent. The ionic liquid [Q+A?] comprises a cation (Q+) selected from the group consisting of 1,3-diisopropylimidazolium, 1,3-diisobutylimidazolium, and 1-isopropyl-3-isobutylimidazolium and an anion (A?) which is not detrimental to the formation of the molecular sieve.

Abstract: A new crystalline molecular sieve designated SSZ-102 having ESV framework topology is disclosed. SSZ-102 is synthesized using an N,N?-dimethyl-1,4-diazabicyclo[2.2.2]octane dication as a structure directing agent.

Abstract: A new crystalline molecular sieve designated SSZ-27 is disclosed. SSZ-27 is synthesized using a hexamethyl [4.3.3.0] propellane-8,11-diammonium cation as a structure directing agent.

Abstract: A method for making a new crystalline molecular sieve designated SSZ-27 is disclosed. SSZ-27 is synthesized using a hexamethyl [4.3.3.0] propellane-8,11-diammonium cation as a structure directing agent.

Abstract: Small crystal LTL framework type zeolites, characterized as polycrystalline aggregates, each of the aggregates comprising a plurality of spherical or cube-like crystallites and wherein each crystallite has an average crystallite size of from 10 to 50 nm, are disclosed. Such zeolites can be prepared by hydrothermal conversion of FAU framework type zeolites at low H2O/SiO2 mole ratios.

Abstract: 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.

Abstract: A method for making a new crystalline molecular sieve designated SSZ-102 is disclosed using an N,N?-dimethyl-1,4-diazabicyclo[2.2.2]octane dication as a structure directing agent. SSZ-102 has ESV framework topology.

Abstract: Crystalline molecular sieves and their synthesis using quaternary N-methyl-diisoalkylammonium cations as organic structure directing agents are disclosed. The structure directing agent has the following structure (1): in which R1 is selected from hydrogen, a methyl group, an ethyl group, a propyl group, and a hydroxymethyl group; and R2, R3, R4 and R5 are independently selected from a methyl group, an ethyl group, and a propyl group.