Abstract: The present invention relates to a method for the preparation of a molecular sieve of the CHA-type as well as catalytic applications thereof.

Abstract: Disclosed is a method of preparing a high-performance zeolite catalyst for reducing nitrogen oxide emissions, and more particularly a technique for preparing a zeolite catalyst, suitable for use in effectively removing nitrogen oxide (NOx), among exhaust gases emitted from vehicle internal combustion engines through selective catalytic reduction (SCR), thereby exhibiting high efficiency, high chemical stability and high thermal durability upon SCR using the prepared catalyst.

Abstract: The invention concerns a process for preparing a copper-comprising microporous aluminosilicate material with AFX structure, comprising at least the steps of mixing, in an aqueous medium, at least one aluminum source, at least one silicon source, at least one copper source, a TETA or TEPA organic complexing agent and a DABCO-C4 structuring agent, in order to obtain a gel, and hydrothermal treatment of said gel with stirring in order to obtain crystallization of said copper-comprising microporous aluminosilicate material with AFX structure.

Abstract: Described is a selective catalytic reduction catalyst comprising a zeolitic framework material of silicon and aluminum atoms, wherein a fraction of the silicon atoms are isomorphously substituted with a tetravalent metal. The catalyst can include a promoter metal such that the catalyst effectively promotes the reaction of ammonia with nitrogen oxides to form nitrogen and H2O selectively over a temperature range of 150 to 650° C. In another aspect, described is a selective catalytic reduction composite comprising an SCR catalyst material and an ammonia storage material comprising a transition metal having an oxidation state of IV. The SCR catalyst material promotes the reaction of ammonia with nitrogen oxides to form nitrogen and H2O selectively over a temperature range of 150° C. to 600° C., and the SCR catalyst material is effective to store ammonia at temperatures of 400° C. and above.

Abstract: The present application provides a ZSM-35 molecular sieve and a preparation method thereof. The ZSM-35 molecular sieve is an aggregated ZSM-35 molecular sieve having a hierarchical macro-meso-microporous pore structure. Raw materials for the preparation method do not include an organic template agent and a crystal seed, and the preparation method includes the following steps: preparing a reactant gel where a molar ratio of SiO2, Al2O3, Na2O, K2O, oxygen-containing acid radical and H2O is (20-40):1.0:(1.5-2.0):(4.0-6.5):(1.0-4.0):(600-1200); sequentially performing an aging treatment and a crystallization treatment on the reactant gel, washing and drying a resulting synthetic product. The ZSM-35 molecular sieve provided by the present application may be obtained by synthesizing without using an organic template agent and crystal seed, and because it has a hierarchical pore structure, it is favorable for material diffusion and mass transfer.

Abstract: A catalyst and process for the production of methyl acetate by contacting dimethyl ether and carbon monoxide in the presence of a catalyst which is a zeolite of micropore volume of 0.01 ml/g or less.

Abstract: The present invention relates to a process for the manufacture of a copper containing small-pore zeolite which comprises?preparing a reaction mixture comprising a zeolite of the faujasite framework type, Cu-tetraethylenepentamine (Cu-TEPA) and at least one compound M(OH)x, which does not comprise the tetraethylammonium cation and?heating the reaction mixture to form a copper containing small-pore zeolite.

Abstract: The present invention refers to a microporous crystalline material, to the method for the production thereof and to the use of same, the material having a composition: xX2O3:zZO2:yYO2 in which: X is a trivalent element such as Al, B, Fe, In, Ga, Cr, or mixtures thereof, where (y+z)/x can have values of between 9 and infinity; Z corresponds to a tetravalent element selected from Si, Ge or mixtures thereof; and Y corresponds to a tetravalent element such as Ti, Sn, Zr, V or mixtures thereof, where z/y can have values of between 10 and infinity.

Abstract: The present invention relates to a process for the preparation of a zeolitic material comprising the steps of: (1) providing a mixture comprising one or more sources for YO2 and one or more alkenyltrialkylammonium cation R1R2R3R4N+-containing compounds as structure directing agent; and (2) crystallizing the mixture obtained in step (1) to obtain a zeolitic material; wherein Y is a tetravalent element, and wherein R1, R2, and R3 independently from one another stand for alkyl; and R4 stands for alkenyl, as well as to zeolitic materials which may be obtained according to the inventive process and to their use.

Abstract: A novel synthetic crystalline molecular sieve designated as SSZ-108 is disclosed. SSZ-108 may be synthesized using a structure directing agent comprising one or more of 1-butyl-1-methylpyrrolidinium cations and 1-butyl-1-methylpiperidinium cations. Molecular sieve SSZ-108 may be used in catalytic and sorptive processes.

Abstract: Methods for forming two-dimensional (2D) zeolite nanosheets include exposing a multi-lamellar (ML) zeolite material including an organic structure directing agent (OSDA) to a mixture including sulfuric acid and hydrogen peroxide under conditions sufficient to remove substantially all of the OSDA from the ML zeolite material; and after exposing the ML zeolite material, treating a solution containing the ML zeolite material to sonication and/or mixing under conditions sufficient to substantially exfoliate layers of the ML zeolite to obtain porous two-dimensional zeolite nanosheets that are substantially free of the OSDA. In some cases, without further treatment such as secondary growth of the zeolite coating layer, a deposit of the OSDA-free nanosheets on polymer support exhibits hydrocarbon isomer selectivity.

Abstract: STA-20, a molecular sieve having a new framework type, is described. STA-20AP (as prepared) can have an alkyl amine, such as trimethylamine, and 1,6-(1,4-diazabicyclo[2.2.2]octane) hexyl cations (from diDABCO-C6) as SDAs. A lower alkyl ammonium hydroxide, such as tetrabutylammonium hydroxide, can be used as a pH modifier for making SAPO STA-20. A calcined product, STA-20C, formed from as made STA-20 is also described. Methods of preparing STA-20, activating STA-20 by calcination, and metal containing calcined counterparts of STA-20 are described along with methods of using STA-20 and metal containing calcined counterparts of STA-20 in a variety of processes, such as treating exhaust gases and converting methanol to olefins are described.

Abstract: The present invention relates to new crystalline zeolite SSZ-52x prepared using a quaternary ammonium cation templating agent, for example, having the structure: wherein X? is an anion which is not detrimental to the formation of the SSZ-52x. SSZ-52x is useful as a catalyst and shows improved durability, particularly with regard to NOx conversion.

Abstract: A method is disclosed for preparing molecular sieve SSZ-85 in the absence of a source of fluoride ions.

Abstract: A rapid synthesis method of a small-crystal-grain ZSM-5 molecular sieve, the method comprising: preparing a mixed silicon-aluminum glue solution, placing the solution in a crystallization kettle for low-temperature nucleation, enabling high-temperature crystallization growth of the solution, and obtaining a crystallization product, namely, a small-crystal-grain ZSM-5 molecular sieve, the nucleation temperature being 60-120° C., nucleation time being 1-3 hours, a crystallization growth temperature being 150-170° C., and crystallization growth time being 1-3 hours. The method is easy to operate, and has a short operation time, thus being able to complete within 6 hours; in addition, the product has uniform grain sizes, is in a mono-dispersed state, and has a high crystallization degree to a submicron degree.

Abstract: A molecular sieve having the framework structure of ZSM-5 is described comprising crystals having an external surface area in excess of 100 m2/g (as determined by the t-plot method for nitrogen physisorption) and a unique X-ray diffraction pattern.

Abstract: Disclosed herein is a new crystalline molecular sieve designated SSZ-104, its synthesis in the presence of a structure directing agent comprising N-cyclohexylmethyl-N-ethylpyrrolidinium cations, and its use as an adsorbent and a catalyst.

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: A method for preparing molecular sieves with a Linde Type A (LTA) topology structure, and molecular sieves obtained thereby are described wherein a structure directing agent comprising a triquaternary cation is contacted with a source of a first oxide of a first tetravalent element or a source of a first oxide of a trivalent element; and a source of an oxide of a pentavalent elements.

Abstract: This invention relates a process for preparing MTT zeolites which process includes the preparation of a sol-gel from an aluminate solution, mixing a structure directing agent with the sol-gel to form a structure directing mixture, mixing a silica with the structure directing mixture to form a reaction mixture, heating the reaction mixture in a microwave reactor to form an initial zeolite, and removing the structure directing agent to form the MTT zeolite. The invention also relates to MTT zeolites produced by the process, including ZSM-23 zeolites, as well as zeolite membranes, coating and catalysts.

Abstract: ZSM-18 is synthesized from a mixture comprising water, a source of an oxide of a tetravalent element (Y), a source of an oxide of a trivalent element (X), a source of a first cation Q selected from either butamethonium cations or N,N,N,-trimethyl-N-butylammonium cations and a source of at least one second cation M, wherein the second cation M is selected from lithium, strontium, sodium, tetraalkylammonium and mixtures thereof when the first cation, Q is butamethonium cations, and wherein the second cation M is tetramethylammonium when the first cation Q is N,N,N,-trimethyl-N-butylammonium cations.

Abstract: The present invention is directed to a process for preparing CHA-type molecular sieves using a colloidal aluminosilicate in the presence of a octahydroindolium-based cationic structure directing agent.

Abstract: In a process for the synthesis of a crystalline molecular sieve material having the EUO framework type, a synthesis mixture is provided suitable for the formation of an EUO framework type molecular sieve and comprising N,N,N,N?,N?,N?-hexamethylhexanediammonium, Q, cations and a colloidal suspension of seed crystals of an EUO framework type molecular sieve. The synthesis mixture is crystallized and an EUO framework type molecular sieve in the form individual crystals and/or aggregates of crystals having an average size, d50, as measured by laser scattering, of less than 15 ?m is recovered from the synthesis mixture.

Abstract: The present invention relates to a titanium silicalite molecular sieve, wherein the crystal grain of the titanium silicalite molecular sieve has a ratio of (surface Si/Ti ratio):(bulk Si/Ti ratio) being larger than 1.1 and less than 5.

Abstract: A novel method for synthesizing AEI zeolites is provided which results in high overall relative yields on silica and the structure directing agent.

Abstract: A method for making a new crystalline molecular sieve designated SSZ-96 is disclosed using a 1-butyl-1-methyl-octahydroindolium cation as a structure directing agent.

Abstract: The present invention is directed to a process for preparing CHA-type molecular sieves using a colloidal aluminosilicate composition containing a cationic structure directing agent selected from the group consisting of N-cyclohexyl-N-methylpyrrolidinium, N-cyclohexyl-N-ethylpyrrolidinium, N-methyl-N-(3-methylcyclohexyl)pyrrolidinium, N-ethyl-N-(3-methylcyclohexyl)pyrrolidinium, N-methyl-N-(2-methylcyclohexyl)-pyrrolidinium, N-ethyl-N-(2-methylcyclohexyl)pyrrolidinium, and mixtures thereof.

Abstract: A method for making zeolite SSZ-35 is disclosed using a N,N-dimethylazonanium cation as a structure directing agent.

Abstract: The present invention is directed to a process for preparing CHA-type molecular sieves using a colloidal aluminosilicate in the presence of a cationic structure directing agent selected from the group consisting of N-cyclohexyl-N-methylpyrrolidinium, N-methyl-N-(3-methylcyclohexyl)pyrrolidinium, N-ethyl-N-(3-methylcyclohexyl)pyrrolidinium, and mixtures thereof.

Abstract: The present invention is directed to a process for preparing MWW-type molecular sieves using 1,3-diisobutylimidazolium as a structure directing agent.

Abstract: A method for making zeolite SSZ-35 is disclosed using a N,N-diethyl-2,3-dimethylpiperidinium cation or a N,N-dimethyl-2-isopropylpiperidinium cation as a structure directing agent.

Abstract: A one step synthesis of nanocrystalline zeolites ZSM-5 and Na? from a single template system in high yield has been discovered. The size of individual nanocrystals, as well as mesopore surface area and pore volume can be controlled by adjusting the pH of the reaction mixture, as well as the hydrothermal treatment temperature and duration. The mesopore volume and size distribution show a dependence on particle size such that smaller particles lead to higher mesopore volumes and narrower pore size distributions.

Abstract: A method is disclosed for preparing zeolite SSZ-70 using an imidazolium cation as a structure directing agent in conjunction with a polyethyleneimine modifier. The SSZ-70 zeolite is characterized as having an external surface area larger than conventional SSZ-70 zeolites.

Abstract: A novel MFI zeolite that when used as a catalyst, can be used for a selective catalytic reaction for larger molecules and provides a method for producing the MFI zeolite. The MFI zeolite includes uniform mesopores having a pore distribution curve which a peak-width thereof at half height (hw) is at most 20 nm (hw?20 nm) and a center value (?) of a maximum peak is 10 nm or more and 20 nm or less (10 nm???20 nm), and having a pore volume (pv) of the uniform mesopores of at least 0.05 mL/g (0.05 mL/g?pv); the MFI zeolite has no peak in a range of 0.1° to 3° in powder X-ray diffraction measurement with a diffraction angle represented by 2?; and the MFI zeolite has an average particle diameter (PD) of at most 100 nm (PD?100 nm).

Abstract: A method for preparing molecular sieves with a Linde Type A (LTA) topology structure, and molecular sieves obtained thereby are described wherein a structure directing agent comprising a triquaternary cation is contacted with a source of a first oxide of a first tetravalent element or a source of a first oxide of a trivalent element; and a source of an oxide of a pentavalent elements.

Abstract: A new family of crystalline microporous metallophosphates designated MAPSO-64 has been synthesized. These metallophosphates are represented by the empirical formula R+rMmn+EPxSiyOz where R is an organoammonium cation such as ETMA+ or DEDMA?, M is a divalent metal such as an alkaline earth or transition metal, and E is a framework element such as aluminum or gallium. The microporous MAPSO-64 compositions BPH topology and have catalytic properties for carrying out various hydrocarbon conversion processes and separation properties for separating at least one component.

Abstract: A new molecular sieve material is designated as EMM-23 and has, in its as-calcined form, an X-ray diffraction pattern including the following peaks in Table 1: TABLE 1 d-spacing (?) Relative Intensity [100 × I/I(o)] 17.5-16.3 60-100 10.6-10.1 5-50 9.99-9.56 20-70? 6.23-6.06 1-10 5.84-5.69 1-10 5.54-5.40 1-10 4.29-4.21 1-10 3.932-3.864 1-10 3.766-3.704 5-40 3.735-3.674 1-10 3.657-3.598 1-10 3.595-3.

Abstract: A crystalline molecular sieve of MFS framework type manufactured by the method disclosed herein. A hydrocarbon conversion process using the crystalline molecular sieve is disclosed.

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: This disclosure is directed to a new cobalt aluminophosphate molecular sieve designated SSZ-85 and a method for preparing SSZ-85 using a 1,3-diisopropylimidazolium ionic liquid.

Abstract: A molecular sieve material designated as EMM-22 has, in its calcined form, an X-ray diffraction pattern including the following peaks in Table 1: TABLE 1 Relative Intensity d-spacing (?) [100 × I/I(o)] 11.03 ± 0.40 VS ?9.91 ± 0.20 W ?6.70 ± 0.04 VW ?4.39 ± 0.02 W ?4.06 ± 0.04 W ?3.85 ± 0.02 M ?3.37 ± 0.

Abstract: Methods are provided for synthesizing ZSM-58 crystals with an improved morphology and/or an improved size distribution. By controlling the conditions during synthesis of the ZSM-58 crystals, crystals of a useful size with a narrow size distribution can be generated. Additionally, by controlling the ratio of water content to silica content in the synthesis mixture, it has unexpectedly been found that ZSM-58 crystals can be formed with an improved morphology. The improved morphology can result in ZSM-58 crystals with a more uniform size across the various dimensions of the crystal, which allows for more uniform diffusion within the crystal. This is in contrast to conventionally synthesized crystals, where the size of the crystal can vary along different axes of the crystals.

Abstract: The present invention is directed to a process for preparing CHA-type molecular sieves using a colloidal aluminosilicate composition containing at least one cyclic nitrogen-containing cation suitable as directing agents for synthesizing CHA-type molecular sieves.

Abstract: An aspect of the invention relates to a method of synthesizing a crystalline molecular sieve having an MSE framework type, the method comprising crystallizing a reaction mixture comprising a source of water, a source of an oxide of a tetravalent element, Y, selected from at least one of silicon, tin, titanium, vanadium, and germanium, optionally but preferably a source of a trivalent element, X, a source of an alkali or alkaline earth metal, M, a source of a tetraethylammonium cation, Q1, and optionally a source of a second organic cation, Q2, which can include a cyclic nitrogen-containing ammonium cation.

Abstract: An aluminosilicate ZSM-12 may be prepared de novo in a small crystalline form from a reaction mixture containing a source of silica and a source of alumina. A small crystalline form of aluminosilicate ZSM-12 may also be prepared from a small crystalline form of borosilicate ZSM-12 by replacement of boron in the borosilicate ZSM-12 framework with aluminum. The aluminosilicate ZSM-12 is useful as an isomerization selective catalyst in processes such as isomerization dewaxing hydrocarbon feedstocks.

Abstract: A method of preparing a mesoporous zeolite material is disclosed. The method comprises forming template-occluded primary metal-doped silicate particles having an amorphous structure and aggregating the particles into mesoporous agglomerates. The amorphous structure is further transformed into a microporous nanocrystalline zeolite structure, thereby forming a mesoporous zeolitic material. Forming the mesoporous zeolite material includes removing the template from the template-occluded particles.

Abstract: A process is described for producing an M41S family molecular sieve. The process comprises preparing a synthesis mixture capable of forming said molecular sieve in a reactor, which is equipped with a mixer having a Froude number of at least 1, said synthesis mixture having a solids content of at least 20 wt %. The synthesis mixture is heated in the reactor while agitating the mixture with said mixer to form a product mixture comprising water and crystals of said molecular sieve material. Thereafter at least part of the water is removed from the product mixture in the reactor so as to decrease the water content of the product mixture inside the reactor by at least 5 wt %.

Abstract: Disclosed herein is method for preparing LEV-type zeolites from FAU-type zeolites in fluoride media using an N-methyl quinuclidinium cation as a structure directing agent.

Abstract: A new family of crystalline microporous metallophosphates designated AlPO-57 has been synthesized. These metallophosphates are represented by the empirical formula R+rMmn+EPxSiyOz where R is an organoammonium cation such as the DEDMA+, M is a divalent framework metal such as an alkaline earth or transition metal, and E is a framework element such as aluminum or gallium. The microporous AlPO-57 compositions are characterized by a new unique ABC-6 net structure and have catalytic properties for carrying out various hydrocarbon conversion processes and separation properties for separating at least one component.

Abstract: A catalyst and its preparation and use are disclosed. The catalyst is a silicalite having germanium (Ge) included within the framework of the silicalite prepared in a particular manner. The catalyst may be used in a method of converting hydrocarbons wherein a hydrocarbon feed is contacted with the catalyst. The catalyst may be formed by preparing an aqueous reaction mixture of a silica-containing silicalite precursor material and a germanium source. The reactants of the reaction mixture are allowed to react. The reacted reaction mixture is heated under conditions to form crystals of a silicalite having germanium included within the framework of the silicalite. The crystals are then calcined to form the catalyst. In certain embodiments, a noble metal may be deposited upon the germanium-containing silicalite.