Abstract: Novel MEL framework type zeolites can be made to have small crystallite sizes and desirable silica/SiO2 molar ratios. Catalyst compositions comprising such MEL framework type zeolites can be particularly advantageous in isomerization C8 aromatic mixtures. An isomerization process for converting C8 aromatic hydrocarbons can advantageously utilize a catalyst composition comprising a MEL framework type zeolite.

Abstract: The present disclosure provides a method of making zeolite intergrowths. In one embodiment, the present disclosure provides a method of making an AEI-based material, including the steps of: preparing a mixture of water, an alumina source, a silica source, a CHA structure directing agent, and an AEI structure directing agent, wherein the molar ratio of the CHA structure directing agent to the AEI structure directing agent is from about 1:1 to about 1:15; heating the mixture at a temperature sufficient to promote formation of crystals; and calcining the crystals at a temperature of from about 450° C. to about 750° C. to obtain a product, wherein no halide-containing reagent is employed. The AEI-based materials of the present disclosure may find particular use in selective catalytic reduction of NOx in exhaust gas streams.

Abstract: Catalytic compositions and sequential catalytic methods are generally described. In some embodiments, a composition comprises a first catalyst comprising a Cu-modified zeolite, and a second catalyst capable of a coupling reaction between (a) an intermediate resulting from a reaction of a reactant at the first catalyst, and (b) a co-reagent, wherein a rate of diffusion of the co-reagent within one or more cages and/or pores of the first catalyst is lower than a rate of diffusion of the intermediate within the one or more cages and/or pores of the first catalyst.

Abstract: In the present disclosure, a heterogeneous nickel-based oligomerization catalyst in which nickel in the form of single atom is loaded on an Al-mesoporous silicate support by ion exchange and a method for producing the same, and a method for oligomerizing light olefins, specifically C4 olefins using the catalyst are described.

Abstract: 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.

Abstract: Catalyst particles comprising one or more active metal components and methods for manufacturing such catalyst particles are provided. The particles are a composite of a granulating agent or binder material such as an inorganic oxide, and an ultra-stable Y (hereafter “USY”) zeolite in which some of the aluminum atoms in the framework are substituted with zirconium atoms and/or titanium atoms and/or hafnium atoms. The one or more active phase components are incorporated prior to mixing the binder with the post-framework modified USY zeolite, extruding the resulting composite mixture, and forming the catalyst particles. The one or more active phase components are incorporated in the post-framework modified USY zeolite prior to forming the catalyst particles.

Abstract: Methods for synthesizing a mesoporous nano-sized ultra-stable Y zeolite include combining a microporous Y zeolite having a SiO2/Al2O3 molar ratio of less than 5.2 with water to form a microporous Y zeolite slurry and heating the microporous Y zeolite slurry to 30° C. to 100° C. to form a heated microporous Y zeolite slurry. Further the method includes adding a 0.1M to 2.0M ammonium hexafluorosilicate solution and a 0.1M to 2.0M ammonium hydroxide solution in a drop-wise manner, either sequentially or simultaneously, to the heated microporous Y zeolite slurry to form a treated zeolite solution and holding the treated zeolite solution at 50° C. to 100° C. Finally the method includes filtering and washing the dealuminated solution with water to form an ultra-stable Y zeolite precursor, drying the ultra-stable Y zeolite precursor, and calcining the dried zeolite precursor to form the nano-sized ultra-stable Y zeolite.

Abstract: The present invention refers to catalysts that are selective for the reaction of ODH of propane to propene. Said catalysts are potassium salts of the dodecatungstophosphate ion partially substituted with vanadium and niobium, or mixed oxides of W, V, and Nb, with a tungsten bronze structure, obtained by thermal decomposition of polyoxometalate salts with a Keggin structure.

Abstract: The present invention further provides a method of making an metal-loaded aluminosilicate zeolite having a maximum pore opening defined by eight tetrahedral atoms from pre-existing aluminosilicate zeolite crystallites, wherein the metal is present in a range of from 0.5 to 5.0 wt. % based on the total weight of the metal-loaded aluminosilicate zeolite.

Abstract: An oxide of sulfur oxygen transfer reagent is provided. A method of producing olefins from hydrocarbons with a concomitant production of water (oxidative dehydrogenation), using the oxide of sulfur oxygen transfer reagent is also provided. The sulfur oxygen transfer reagent can be used as an oxygen transfer reagent, and therefore acts as a non-metal carrier, for oxygen in a redox looping reactor for an oxidative dehydrogenation process such as the conversion of ethane to ethylene. The reduced forms of oxides of sulfur, formed in in this oxidative dehydrogenation process, can be re-oxidized with air and generate useful process heat. Also provided are methods of using the oxide of sulfur oxygen transfer reagent, and an apparatus for effecting the oxidative dehydrogenation of the hydrocarbon feed. Methods of producing the oxide of sulfur oxygen transfer reagent are also provided.

Abstract: Catalyst particles comprising one or more active metal components and methods for manufacturing such catalyst particles are provided. The particles are a composite of a granulating agent or binder material such as an inorganic oxide, and an ultra-stable Y (hereafter “USY”) zeolite in which some of the aluminum atoms in the framework are substituted with zirconium atoms and/or titanium atoms and/or hafnium atoms. The one or more active phase components are incorporated prior to mixing the binder with the post-framework modified USY zeolite, extruding the resulting composite mixture, and forming the catalyst particles. The one or more active phase components are incorporated in the binder material prior to forming the catalyst particles.

Abstract: A method of making a xylene isomerization catalyst comprises the steps of (i) contacting a ZSM-5 zeolite starting material having a silica to alumina molar ratio of 20 to 50 and having a mesopore surface area in the range of 50 m2/gram to 200 m2/gram in a reactor with a base to provide an intermediate zeolite material; (ii) recovering the intermediate ZSM-5 zeolite material of step (i); (iii) contacting the intermediate zeolite material with an acid to provide an acid treated ZSM-5 zeolite product; (iv) recovering the acid treated ZSM-5 zeolite material; and (v) calcining the acid treated ZSM-5 zeolite material to provide a desilicated ZSM-5 zeolite product having a silica to alumina molar ratio of 20 to 150 and having a mesopore surface area in the range of 100 m2/gram to 400 m2/gram.

Abstract: The present disclosure provides a catalyst for SRO reactions. The catalyst includes a solid acid material and a metal. In this case, pores of the catalyst corresponding to at least 20% of the total pore volume of the catalyst have a pore size of 10 nm or more. The present disclosure also provides a method of using the catalyst.

Abstract: A high-strength zeolite molding includes 10 parts by weight or more and 40 parts by weight or less of clay relative to 100 parts by weight of zeolite, and having a compressive strength of 20 N or more, in which the zeolite contains at least one zeolite that has Si/Al2 of 300 or more and 100000 or less and a water adsorption amount of 10 (g/100 g) or less under conditions of 25° C. and a relative pressure of 0.5, and the clay contains at least one clay that has a solid acidity of 0.15 mmol/g or less as determined by a NH3-TPD method. A method for producing includes kneading, molding, drying and disintegrating a product and then firing at 400° C. or higher and 700° C. or lower.

Abstract: Methods for synthesizing a mesoporous nano-sized zeolite beta are described. The method may include mixing an aqueous base solution with hexadecyltrimethylammonium bromide (CTAB) to form a first solution; adding nano-sized zeolite particles having a particle size of less than or equal to 100 nm to the first solution to form a second solution. The nano-sized zeolite particles include a microporous framework with a plurality of micropores having diameters of less than or equal to 2 nm and a BEA framework type. The method may further include transferring the second solution to an autoclave operated at 25° C. to 200° C. for 3 to 24 hours to form a colloid; drying the colloid at 100° C. to 200° C. for 8 to 36 hours without washing the colloid to form a zeolite precursor; and calcining the zeolite precursor at 250° C. to 600° C. for 1 to 8 hours to form the mesoporous nano-sized zeolite beta.

Abstract: Methods for synthesizing a mesoporous nano-sized ultra-stable Y zeolite include adding sodium aluminate and colloidal silica to an aqueous NaOH solution and mixing to form a hydrogel having a molar ratio composition of 8 to 12 Na2O:Al2O3:14 SiO2:200 to 400 H2O. The method further includes heating the hydrogel to an autoclave to form a zeolite precursor which is filtered and washed to form a nano-sized Y zeolite. Further the method includes combining the nano-sized Y zeolite with water to form a nano-sized Y zeolite slurry mixture and then adding a 0.1 to 2.0 M aqueous solution of ammonium hexafluorosilicate to form a dealuminated solution. Finally the method includes filtering and washing the dealuminated solution with water to form an ultra-stable Y zeolite precursor, drying the ultra-stable Y zeolite precursor, and calcining the dried zeolite precursor to form the nano-sized ultra-stable Y zeolite.

Abstract: The present invention concerns a zeolitic adsorbent agglomerate comprising at least one zeolite of faujasite type comprising sodium and/or lithium and/or calcium, and/or barium and/or potassium, of porosity between 25% and 45%, and having a standard deviation ? of crystal size distribution in said agglomerate of less than 0.30 ?m. The invention also concerns the use of the zeolitic adsorbent agglomerate to separate hydrocarbon mixtures, and the process to separate hydrocarbon mixtures using said zeolitic adsorbent agglomerate.

Abstract: The present disclosure relates to the catalytic field, and discloses a catalyst system and a light hydrocarbon aromatization method, a carbon dioxide hydrogenation process and a method for enhancing the catalytic activity and/or lifetime of the catalyst during a heterogeneous catalysis process, the catalyst system comprising a porous material layer containing an active metal component and a molecular sieve layer. The catalyst system provided by the present disclosure exhibits desirable catalytic activity, stability, renewability and selectivity, thus has significant benefits.

Abstract: Hydrotreating catalysts are provided having one or more phosphorus components carried on a composite support of a titanium-loaded binder component and post-framework modified ultra-stable Y-type zeolite. The support comprises the titanium-loaded binder component and a post-framework modified ultra-stable Y-type (USY) zeolite in which a portion of aluminum atoms constituting a zeolite framework thereof is substituted with zirconium atoms and/or titanium atoms and/or hafnium atoms. The active components including the phosphorous active component and one or more hydrocracking metals active components loaded on the support.

Abstract: The present disclosure provides molecular sieves with intergrown phases of AEI and CHA topologies and a catalyst thereof. A preparation method for the molecular sieves include the following steps: mixing a hydroxyphosphono organic alkali R with an aluminum source and a silicon source to obtain a sol-gel precursor, putting the sol-gel precursor into a closed hydrothermal synthesis reactor for reaction, filtering the reaction solution, washing, drying, and calcination to obtain the molecular sieves with intergrown phases of AEI and CHA topologies. The molecular sieves and the catalyst thereof can be directly synthesized under mild conditions with a hydroxyphosphono organic alkali as a structure-directing agent and a phosphorus source, have a pH value of 6-9 and low requirements for corrosion resistance of production devices, and are suitable for large-scale production.