Abstract: The present invention provides an improved catalytic fast pyrolysis process for increased yield of useful and desirable products. In particular, the process comprises an improved catalytic fast pyrolysis process for producing aromatic compounds, such as, for example, benzene, toluene and xylenes, from biomass feedstock containing impurities, such as, for example alkali and alkaline earth metal, sulfur and nitrogen components.

Abstract: The present invention relates to granulated particles with improved attrition and a method for producing granulated particles by fluidized bed granulation of inorganic particles wherein particles of reduced particle size are fed into a fluldized-bed granulation reactor thereby producing granulated particles with improved attrition.

Abstract: The invention is directed to a process to prepare propylene from a hydrocarbon feed comprising pentane by contacting the hydrocarbon feed with a heterogeneous cracking catalyst as present in one or more fixed beds thereby obtaining a cracked effluent. The heterogeneous catalyst comprises a matrix component and a molecular sieve comprising framework alumina, framework silica and a framework metal selected from the group of Zn, Fe, Ce, La, Y, Ga and/or Zr. Propylene is isolated from the cracked effluent.

Abstract: A multi-functional composite catalyst includes a catalyst support material, a preformed catalyst material at least partially secured in the catalyst support, and at least one catalytically active compound supported by the catalyst support, the preformed catalyst material, or both. The catalyst support material may include fumed silica, alumina, fumed alumina, fumed titania, or combinations of these. A catalytic activity of the catalytically active compound may be different than a catalytic activity of the preformed catalyst material. The composite catalyst may be catalyst for producing propene from 2-butene and may include a zeolite as the preformed catalyst material and a metal oxide, such as tungsten oxide, as the catalytically active material.

Abstract: A method for the treatment of silicon-containing wastewater from the preparation of a molecular sieve or a catalyst includes the step of contacting the silicon-containing wastewater with at least one acid or at least one alkali, so that at least a part of the silicon elements in the silicon-containing wastewater form a colloid. A mixture containing a colloid is thus obtained. A silicon-containing solid phase and a first liquid phase are produced by a solid-liquid separation. A solid phase and a second liquid phase are produced by a solid-liquid separation after at least a part of the metal elements in the first liquid phase form a precipitate. At least a part of the second liquid phase is subjected to electrodialysis to produce an acid liquor and/or an alkali liquor. The silicon-containing solid phase can be used as the raw material for a molecular sieve synthesis.

Abstract: The present disclosure provides a sound absorbing material. The sound absorbing material comprises MFI-structural-type zeolite. The MFI-structural-type zeolite comprises a framework, and the framework comprises SiO2 and AlO3, and the mass ratio of Si to Al in the framework is less than 200 and not less than 50. The present disclosure also provides a speaker box applying the sound absorbing material. The sound absorbing material provided by the present disclosure and the speaker box using the sound absorbing material can further improve the performance of the speaker box, reduce the failure of zeolite and improve the performance stability of the speaker box.

Abstract: This invention relates to core-shell nanoparticles having acid sites, a method of manufacturing the same, and a method of directly producing hydrogen peroxide using the same.

Abstract: A carbon dioxide adsorbent including a hierarchical zeolite. The hierarchical zeolite defines micropores having a pore width between about 0.4 nm and about 2 nm, and at least one of: mesopores having a pore width between about 2 nm and about 50 nm; and macropores having a pore width greater than about 50 nm.

Abstract: A new family of a microporous crystalline metallophosphate-based materials designated AlPO-75 has been synthesized. These metallophosphate-based materials are represented by the empirical formula Rp+rMw2+ExPSiyOz where R is a quaternary ammonium cation such as N,N,N?,N?-tetramethyl-N,N?-p-xyleno-1,6-hexanediammonium, M is a divalent framework metal such as magnesium or zinc, E is a framework element such as aluminum or gallium and the framework may optionally contain silicon. The microporous AlPO-75 compositions are characterized by having the SAO topology and have catalytic properties for carrying out various hydrocarbon conversion processes and separating properties for separating at least one component.

Abstract: A new family of a microporous crystalline metallophosphate-based materials designated SAPO-80 has been synthesized. These metallophosphate-based materials are represented by the empirical formula Rp+rMw2+ExPSiyOz where R is a quaternary ammonium cation such as ?,??-bis(dimethylethylammonium)-p-xylene, E is a framework element such as aluminum or gallium and the framework may optionally contain a divalent framework metal M such as magnesium or zinc. The microporous SAPO-80 compositions are characterized by having the AFX topology and have catalytic properties for carrying out various hydrocarbon conversion processes and separating properties for separating at least one component.

Abstract: The present invention relates to a process for the direct synthesis of a material with a CHA zeolite structure in the silicoaluminate form thereof containing copper atoms, which comprises at least the following steps: (i) Preparation of a mixture which contains at least one water source, one copper source, one polyamine, one source of Y tetravalent element, one source of X trivalent element, the tetraethylammonium cation as the only OSDA and one source of alkaline or alkaline earth (A) cations, and wherein the synthesis mixture has the following molar composition: YO2:aX2O3:bOSDA:cA:dH2O:eCu:fpolyamine (ii) Crystallization of the mixture obtained in (i) in a reactor; (iii) Recovery of the crystalline material obtained in (ii).

Abstract: Methods of simultaneously converting butanes and methanol to olefins over Ti-containing zeolite catalysts are described. The exothermicity of the alcohols to olefins reaction is matched by endothermicity of dehydrogenation reaction of butane(s) to light olefins resulting in a thermo-neutral process. The Ti-containing zeolites provide excellent selectivity to light olefins as well as exceptionally high hydrothermal stability. The coupled reaction may advantageously be conducted in a staged reactor with methanol/DME conversion zones alternating with zones for butane(s) dehydrogenation. The resulting light olefins can then be reacted with iso-butane to produce high-octane alkylate. The net result is a highly efficient and low cost method for converting methanol and butanes to alkylate.

Abstract: A method is provided for synthesizing molecular sieves of ITE framework type using one or more of 1-ethyl-1,3,5-trimethylpiperidinium cations and 1-ethyl-1-methyldecahydroquinolinium cations a structure directing agent.

Abstract: The present invention relates to a PST-20 zeolite having a novel skeletal structure, its preparation method, and a selective separation and adsorption method for a gas using the PST-20 zeolite. More specifically, the present invention relates to a method of preparing a microporous aluminosilicate PST-20 zeolite having a novel skeletal structure totally different from the skeletal structure of known zeolites and using the PST-20 zeolite as an adsorbent/separator capable of selectively adsorbing/separating carbon dioxide to separate and collect carbon dioxide with high purity from burned gases or natural gases.

Abstract: A method is provided for synthesizing zeolite SSZ-31 using 2-ethyl-N,N,N-trimethylbutan-1-aminium cations as a structure directing agent.

Abstract: The present invention relates to a process for hydroxylation of a compound of formula (I) by reacting the compound of formula (I) with an oxidizing agent, in the presence of a titanium silicalite zeolite prepared by crystallization preceded by a maturing step. The present invention also relates to a titanium silicalite zeolite and to the process for preparing same.

Abstract: The present disclosure is directed to a high-silica form of zeolite SSZ-32x, its synthesis in fluoride media using dipropylamine as a structure directing agent, and its use in catalytic processes.

Abstract: A gas adsorbent includes copper-exchanged ZSM-5 zeolite, and the crystallinity of the copper-exchanged ZSM-5 zeolite is set to at least 40% and up to 80%.

Abstract: The present invention pertains to the field of molecular sieve synthesis, and relates to a synthesis method of ZSM-5 type molecular sieves. In this method, natural minerals, i.e., natural kaolin and natural diatomite, are used as the total silicon source and aluminum source required for the molecular sieve synthesis, and these two natural minerals are calcinated and subjected to acidic (alkaline) treatment before they are mixed at a certain ratio, and then crystallized under hydrothermal conditions to obtain the product, a ZSM-5 type molecular sieve. The ZSM-5 type molecular sieve obtained by the method according to the present invention is a hierarchical porous material having a crystallinity of 70% to 120% as compared to conventional ZSM-5 type molecular sieves synthesized by using pure chemical reagents, and the silica-to-alumina ratio in the molecular sieve product may be adjusted by varying the ratio of the two minerals in the raw materials for the synthesis.

Abstract: The present disclosure relates to a preparing method of a zeolite core/silica zeolite shell composite, which includes adding a zeolite seed crystal into a gel solution containing a silicon-source compound, a structure directing agent and a fluorine anion-source compound, and then, crystallizing the gel solution for growing a silica zeolite shell containing a crystal structure which is coherent with that of the zeolite seed crystal; a zeolite core/silica zeolite shell composite prepared by the preparing method above; and catalytic use of the zeolite core/silica zeolite shell composite.

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. A method for selectively reducing nitrogen oxides and an exhaust gas treatment system are also described.

Abstract: A zeolite has a CHA structure, a SiO2/Al2O3 composition ratio less than 15, and potassium in an amount of about 0.1% by mass to about 1% by mass in terms of K2O.

Abstract: In a process for producing a phosphorus-modified zeolite catalyst, an aqueous reaction mixture comprising a source of silica and a source of an organic directing agent effective to direct the synthesis of a desired zeolite is heated at a temperature and for a time sufficient to produce crystals of the desired zeolite. Wet zeolite crystals can then be separated from the reaction mixture and, without removing all the water from the wet zeolite crystals, the zeolite can be converted into the ammonium form by ion exchange, and the crystals can be treated with a phosphorus compound. The phosphorus-treated, ammonium-exchanged zeolite can then be formed into a catalyst to be heated in one or more stages to remove the water and organic directing agent from the zeolite crystals and to convert the zeolite to the hydrogen form.

Abstract: A method is disclosed for synthesizing molecular sieve SSZ-98 using a structure directing agent selected from one or more of 1,1-diethylpyrrolidinium cations, 1-butyl-1-methylpiperidinium cations, 1,1-diethyl-4-methylpiperidinium cations, and 8-(pyridin-2-yl)-5,8-diazaspiro[4.5]decan-5-ium cations.

Abstract: A ceramic separation membrane structure in which a zeolite separation membrane formed on a ceramic porous body is repaired, and a repair method thereof. In the ceramic separation membrane structure, a zeolite separation membrane is disposed on a ceramic porous body, and defects of the zeolite separation membrane are repaired by zeolite repaired portions containing zeolite of structure different from the structure of zeolite of the zeolite separation membrane. The zeolite separation membrane and the zeolite repaired portions are made of a hydrophobic zeolite having a ratio of SiO2/Al2O3=100 or more.

Abstract: A method is disclosed for making LEV framework type zeolites using N,N?-dimethyl-1,4-diazabicyclo[2.2.2]octane dications as a structure directing agent.

Abstract: The invention relates to: a ?-type iron silicate which has a fluorine content not more than 400 ppm by weight on a dry basis and in which the crystal grains have a truncated square bipyramidal morphology in an examination with a scanning electron microscope and the whole or part of the iron is contained in the ?-type framework structure, and a process for producing the iron silicate; anther ?-type iron silicate, and a process for producing the iron silicate; and a nitrogen oxide removal catalyst containing the other ?-type iron silicate, a process for producing the catalyst, and a method for nitrogen oxide removal with the catalyst.

Abstract: The present invention relates to a process for the preparation of a zeolitic material having a structure comprising YO2 and optionally comprising X2O3, preferably comprising YO2 and X2O3, wherein said process comprises the steps of (1) providing a mixture comprising one or more ammonium compounds of which the ammonium cation has the formula (I): [R1R2NR3R4]+??(I) and further comprising one or more sources for YO2 and one or more sources for X2O3; (2) crystallizing the mixture provided in (1); wherein Y is a tetravalent element, and X is a trivalent element, and wherein in formula (I) R1 and R2 are independently from one another derivatized or underivatized methyl, and R3 and R4 are independently from one another derivatized or underivatized (C3-C5)alkyl, and wherein the molar ratio of ammonium cation having the formula (I) to Y in the mixture provided in step (1) and crystallized in step (2) is equal to or greater than 0.25.

Abstract: A method for preparing an MAZ framework type zeolite is disclosed using a trimethylphenylammonium cation as a structure directing agent. The MAZ framework type zeolite, in its as-synthesized form, contains in its intracrystalline pores the trimethylphenylammonium cation. The resultant MAZ framework type zeolite crystals have an average crystallite size of greater than 5 ?m.

Abstract: The present invention provides a catalytic cracking catalyst, processing method and use thereof. When the catalyst is added into a commercial catalytic cracking unit, it has an initial activity of not higher than 80, preferably not higher than 75, more preferably not higher than 70, a self-balancing time of 0.1-50 h, and an equilibrium activity of 35-60. Said method enables the activity and selectivity of the catalyst in the catalytic cracking unit to be more homogeneous and notably improves the selectivity of the catalytic cracking catalyst, so as to obviously reduce the dry gas and coke yields, to sufficiently use steam and to reduce the energy consumption of the FCC unit.

Abstract: Provided is a method for producing a MAZ-type zeolite, the method having an environmental impact which has been reduced as much as possible while not using a structure-directing agent as far as possible. In the method for producing a MAZ-type zeolite according to the present invention: (1) a silica source, an alumina source, an alkali source and water are mixed so as to form a reaction mixture that has a composition represented by a specific molar ratio; (2) a MAZ-type zeolite, which has a SiO2/Al2O3 ratio of 5-10, has an average particle diameter of at least 0.1 ?m and does not contain an organic compound, is added, as a seed crystal, into the reaction mixture in an amount of 0.1-30 weight % relative to the silica components in the reaction mixture; and (3) the reaction mixture, into which the seed crystal has been added, is heated at 80-200° C. in a closed system.

Abstract: The disclosure provides methods and materials for preparing a titania nanoparticle product. For example, titania nanoparticle products having desirable optical properties such as a desirable refractive index are prepared according to the methods provided herein.

Abstract: Provided is a method that is for producing a PAU zeolite and that can have an environmental impact that is reduced while, as much as possible, not using a structure-defining agent. The method for producing a PAU zeolite produces by means of (1) mixing a silica source, an alumina source, an alkali source, and water in a manner so as to result in a reaction mixture having a composition represented by a specific mole ratio, (2) using as the seed crystal a PAU zeolite that does not contain organic compounds and has a SiO2/Al2O3 ratio of 4-15 and an average particle size of at least 100 nm, and adding same to the reaction mixture at a ratio of 0.1-20 wt % with respect to the silica component in the reaction mixture, and (3) subjecting the reaction mixture to which the seed crystal has been added to sealed-vessel heating at 80-200° C.

Abstract: The invention relates to a new process which allows the preparation of TS-1 zeolites in a pure phase and with a crystallinity higher than 95%, operating at reduced reaction volumes, and obtaining high productivities and extremely high crystallization yields. The particular crystalline form of the TS-1 zeolite thus prepared, is also described.

Abstract: This invention is for a catalyst for conversion of hydrocarbons. The catalyst contains a zeolite having germanium and at least one selected from the group consisting of tin and boron incorporated into the zeolite framework and at least one metal selected from Group 10 deposited on the zeolite. The catalyst is prepared by synthesizing a zeolite having germanium and at least one selected from the group consisting of tin and boron incorporated into the zeolite framework; depositing the metal; and calcining after preparation of the zeolite and before or after depositing the metal. The catalyst may be used in a process for the conversion of hydrocarbons, such as propane to aromatics, by contacting the catalyst with alkanes having 2 to 12 carbon atoms per molecule and recovering the product.

Abstract: A process for preparing an alkylaromatics isomerisation catalyst comprising at least 0.01% wt of platinum on a carrier comprising of from 1 to 9 wt % of ZSM-12 and inorganic binder, which process comprises treating the carrier with an impregnation solution comprising a cationic platinum compound and having a pH of more than 9, and subsequently drying and calcining the impregnated carrier at a temperature of from 200 to 420° C.; and a process for the isomerisation of alkylaromatics with the help of catalyst thus obtained.

Abstract: The present invention relates to a metal silicoaluminophosphate molecular sieve MeAPSO with a RHO framework structure and a preparation method thereof. The metal silicoaluminophosphate molecular sieve is characterized in that: the metal atoms are at least one of vanadium, copper, molybdenum, zirconium, cobalt, manganese, magnesium, iron, nickel and zinc. The chemical composition of said metal silicoaluminophosphate molecular sieve in anhydrous state is expressed as: mR.nMe.(SixAlyPz)O2, where R represents template existed in molecular sieve micropores, m is the molar number of said template per one molar of (SixAlyPz)O2, m=0.1˜0.5; Me represents metal atom entering into said metal silicoaluminophosphate molecular sieve framework, n is the molar number of Me per one molar of (SixAlyPz)O2, n=0.001˜0.30. Said metal silicoaluminophosphate molecular sieve has ion exchange performance and adsorption performance.

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 new family of crystalline microporous metallophosphates designated AlPO-67 has been synthesized. These metallophosphates are represented by the empirical formula R+rMm2+EPxSiyOz where R is an organoammonium cation such as the ETMA+ or DEDMA+, M is a framework metal alkaline earth or transition metal of valence 2+, and E is a trivalent framework element such as aluminum or gallium. The AlPO-67 compositions exhibit the LEV framework topology and have catalytic properties for carrying out various hydrocarbon conversion processes and separation properties for separating at least one component.

Abstract: A new family of crystalline aluminosilicate zeolites has been synthesized that has been designated UZM-43. These zeolites are similar to previously known ERS-10, SSZ-47 and RUB-35 zeolites but are characterized by unique x-ray diffraction patterns and compositions and have catalytic properties for carrying out various hydrocarbon conversion processes. Catalysts made from these zeolites are useful in hydrocarbon conversion reactions.

Abstract: A new family of crystalline microporous metallophosphates designated AlPO-59 has been synthesized. These metallophosphates are represented by the empirical formula R+rMm2+EPxSiyOz where R is an organoammonium cation such as the ETMA+, M is a framework metal alkaline earth or transition metal of valence 2+, and E is a trivalent framework element such as aluminum or gallium. The AlPO-59 compositions are characterized by a new unique ABC-6 net structure and compositions and have catalytic properties for carrying out various hydrocarbon conversion processes and separation properties for separating at least one component.

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 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: There is provided a water vapor adsorbent for adsorption heat pumps that has high adsorption and desorption performance and high water resistance, such as submersion resistance. The water vapor adsorbent contains a zeolite that contains at least a silicon atom, an aluminum atom, and a phosphorus atom in its framework structure and that has a framework density of 12.0 T/1,000 cubic angstroms or more and 16.0 T/1,000 cubic angstroms or less, wherein the water vapor adsorbent contains a group 11 metal of the periodic table, which constitutes 0.1% to 15% by weight of the zeolite. In the zeolite containing the group 11 metal, an ion of the group 11 metal substitutes for a Bronsted acid site, which promotes a hydrolysis reaction of the zeolite, and decreases the number of Bronsted acid sites of the zeolite, thereby improving the water resistance, such as submersion resistance, of the zeolite.

Abstract: The present invention provides an improved method for manufacturing high quality porous crystalline MCM-56 material. It also relates to the MCM-56 material manufactured by the improved method, catalyst compositions comprising same and use thereof in a process for catalytic conversion of hydrocarbon compounds. One such conversion process involves production of monoalkylated aromatic compounds, particularly ethylbenzene and cumene, by the liquid or partial liquid phase alkylation of alkylatable aromatic compound, particularly benzene.

Abstract: A subject for the invention is to provide a highly heat-resistant SCR catalyst which has an NOx reduction percentage of 40% or higher at 200° C. after a hydrothermal durability treatment. The invention relates to use of ?-type zeolite which has an SiO2/Al2O3 molar ratio of 20 or higher but less than 30 and a crystallite diameter before a hydrothermal durability treatment of 20 nm or larger, shows a change in crystallite through the hydrothermal durability treatment of less than 10%, and has a fluorine content lower than 0.1%. The ?-type zeolite can be crystallized from a liquid reaction mixture containing a secondary and/or a tertiary alkylamine having 5 or more carbon atoms.

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: Disclosed are a novel NU-85 molecular sieve having a specific surface area ranging from about 405 m2/g to about 470 m2/g and a pore volume ranging from about 0.27 cm3/g to about 0.35 cm3/g, and processes for preparing the NU-85 molecular sieve.

Abstract: A new family of crystalline aluminosilicate zeolites has been synthesized designated UZM-45. These zeolites are represented by the empirical formula. Mmn+Rrp+Al(1-x)ExSiyOz where M is an alkali, alkaline earth, or rare earth metal such as lithium and strontium, R is an organoammonium cation such as the choline cation and E is a framework element such as gallium. These zeolites are characterized by unique x-ray diffraction patterns and compositions and have catalytic properties for carrying out various hydrocarbon conversion processes.

Abstract: The present invention relates to a SAPO-34 molecular sieve having both micropores and mesopores and synthesis method thereof. The mesopore diameter in the molecular sieve is in a range of 2-10 nm and the mesopore volume thereof is 0.03-0.3 cm3/g. Triethylamine is used as a template agent and the pore size modifiers are added to the synthesis gel at the same time in the synthesis process, thereby the prepared molecular sieve crystals have mesopore distribution besides micropores. The SAPO-34 molecular sieve synthesized in the present invention can be used as catalysts for conversion of oxygen-containing compounds to lower olefins.