B01J29/86

Delamination of borosilicate layered zeolite

Provided is a surfactant-free, single-step synthesis of delaminated aluminosilicate zeolites. The process comprises the step of heating a borosilicate zeolite precursor in a metal salt solution, e.g., an aluminum nitrate solution, zinc nitrate solution or manganese nitrate solution. The delaminated aluminosilicate zeolite product is then recovered from the solution.

Methods for producing crystalline microporous solids with IWV topology and compositions derived from the same

This disclosure relates to new crystalline microporous solids (including silicate- and aluminosilicate-based solids), the compositions comprising 8 and 10 membered inorganic rings, particularly those having IWV topologies having a range of Si:Al ratios, methods of preparing these and known crystalline microporous solids using certain quaternized imidazolium cation templates.

Olefin oligomerization using delaminated zeolite supports as catalyst

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.

Olefin oligomerization using delaminated zeolite supports as catalyst

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.

Process for preparing propylene oxide

A continuous process for the preparation of propylene oxide, comprising (i) providing a liquid feed stream comprising propene, hydrogen peroxide, acetonitrile, water, optionally propane, and at least one dissolved potassium salt; (ii) passing the feed stream provided in (i) into an epoxidation reactor comprising a catalyst comprising a titanium zeolite of structure type MWW, and subjecting the feed stream to epoxidation reaction conditions in the epoxidation reactor, obtaining a reaction mixture comprising propylene oxide, acetonitrile, water, the at least one potassium salt, optionally propene, and optionally pane; (iii) removing an effluent stream from the epoxidation reactor, the effluent stream comprising propylene oxide, acetonitrile, water, at least a portion of the at least one potassium salt, optionally propene, and optionally propane.

Oxide materials and synthesis by fluoride/chloride anion promoted exfoliation

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.

Oxide materials and synthesis by fluoride/chloride anion promoted exfoliation

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.

Zeolite SSZ-57 having enhanced large pore selectvity

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.

Zeolite SSZ-57 having enhanced large pore selectvity

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.

CATALYST SYSTEMS AND METHODS OF USE

According to embodiments, methods for the production of boron-silicalite-1 are disclosed. In embodiments, the method may include combining a mineralizer agent, a templating agent, water, and boric acid in a first microwave unit; heating the first microwave unit to form a boron-zeolite; calcining the boron-zeolite to form an alkali-zeolite; combining the alkali-zeolite with ammonium nitrate to produce an ion-exchanged zeolite; heating the ion-exchanged zeolite to form a protonated zeolite; and calcining the protonated zeolite to form the boron-silicalite-1. In embodiments, the method may include combining a templating agent, water, and boric acid in a first hydrothermal unit; heating the first microwave unit to form a boron-zeolite; calcining the boron-zeolite to form an alkali-zeolite; combining the alkali-zeolite with ammonium nitrate to produce an ion-exchanged zeolite; heating the ion-exchanged zeolite to form a protonated zeolite; and calcining the protonated zeolite to form the boron-silicalite-1. The boron-silicalite-1 may be microscale or nanoscale.