Abstract: This invention relates to a new synthetic porous crystalline material, designated MCM-68, a method and novel polycyclic organic cation for its preparation and its use in catalytic conversion of organic compounds. The new crystalline material exhibits a distinctive X-ray diffraction pattern and has a unique crystal structure which contains at least one channel system, in which each channel is defined by a 12-membered ring of tetrahedrally coordinated atoms, and at least two further, independent channel systems, in each of which each channel is defined by a 10-membered ring of tetrahedrally coordinated atoms, wherein the number of unique 10-membered ring channels is twice the number of 12-membered ring channels.

Abstract: Zeolites containing silicon, titanium and tellurium oxides are prepared by a hydrothermal method which yields materials containing exceptionally high levels of catalytically active Ti species. Following calcination, the molecular sieves are active and selective catalysts for the epoxidation of olefins using hydrogen peroxide or organic hydroperoxide. The zeolites may have framework structures of varying topology, including MFI, MEL, BEA, ZSM-48, MTW or MCM-41.

Abstract: Low temperature hydrothermal treatment of an LTL zeolite-producing mixture produces a colloidal suspension of the zeolite; the suspension may be used as seeds in Al-- and Ga--LTL zeolite manufacture.

Abstract: The present invention relates to a process for the synthesis of flyash based zeolite-Y (FAZ-Y), comprising grainding and mixing of flyash with caustic soda in a ratio ranging between 1:0.4-1:1.2 to obtain a fine homogenous fusion mixture, heating the said fusion mixture in an invert vessel at about 500-600.degree. C. for about 1-2 hours to obtain a fused mass, cooling, milling, and mixing of the said fused mass in distilled water for about 8-12 hours, subjecting the said slurry to hydrothermal crystallization at about 90-110.degree. C. for 8 to 12 hours to obtain FAZ-Y crystals, washing the said crystals with water and then subjecting the washed crystals to oven drying at 50-60.degree. C. to obtain the desired FAZ-Y crystals.

Abstract: Semi-crystalline alumina compositions with framework mesopores are disclosed. The compositions are assembled from inorganic aluminum precursors and nonionic polyethylene oxide surfactants. The new assembly pathway introduces several new concepts to alumina mesostructure synthesis. The application of low-cost, non-toxic and biodegradable surfactants and low cost aluminum reagents as alumina precursors which are inorganic and low solution reaction temperatures, introduces efficient and environmentally clean synthetic techniques to the formation of mesostructures. Recovery of the surfactant can be achieved through solvent extraction where the solvent may be water or ethanol or by calcination.

Abstract: The invention concerns an inorganic aluminum-based polymer and another element chosen from amongst silicon, titanium and zirconium. The polymer material is obtained from hydrolisable salts and/or compounds such as alcoxides. Application to the production of ancillary layers in photographic products.

Abstract: A process of modifying the porosity of an aluminosilicate or silica whose porosity is not amenable to modification by acid extraction. The process involves contacting said aluminosilicate or silica with an alkali aluminate, and then extracting the aluminate-treated material with an extraction agent so as to form the porosity-modified aluminosilicate or silica. The process is applicable to zeolites which are unreactive under acid extraction conditions, e.g. ferrierite, and applicable to zeolites which are structurally unstable under acid extraction conditions, such as the mineral bikitaite. Mesoporous compositions are disclosed, including a mesoporous ferrierite and a mesoporous zeolite DCM-3.

Abstract: A new family of crystalline and microporous compositions having indium and silicon as essential framework elements have been synthesized. These compositions are characterized by unique x-ray diffraction patterns and an empirical formula of:A.sub.p (In.sub.1-n M.sub.n).sub.y Si.sub.1-z Ge.sub.z O.sub.xwhere A is a cation such as sodium or potassium and M is a metal having a valence of +3, +4 or +5 such as iron (+3), titanium (+4) and niobium (+5).

Abstract: A composition of matter represented by the formulaM.sup.n+.sub.(2x+y)/n [Si.sub.(2-x-y) Al.sub.(y) Zn.sub.(x) ]O.sub.4 ;whereinM is cation selected from Groups 1, 2, 7, 10, 11, 12 and the f block elements as defined by the Periodic Table of the elements as adopted by IUPAC; n is the valence of the selected cation; M; x is greater than or equal to 0.02 but less than or equal to 1;y is a value less than or equal to 0.98; and 2x+y is greater than or equal to 0.80;wherein the composition of matter has the FAU structure. The compositions have utility as gas separation adsorbents in processes for separating oxygen from nitrogen in air.

Abstract: An oxygen scavenging composition composed of a carrier and a metal coated, inert, porous particulate material having the metal substantially in a zero valence state. The composition is contained within the interior cavity of a container to scavenge oxygen therein. The composition may form at least a part of the interior surface of the container or be present therein in the form of a film, mat, sachet or ceramic.

Abstract: Applicants have prepared a novel zeolite identified as LZ-281. This zeolite has the framework topology of zeolite EMT. The LZ-281 zeolite is prepared by removing framework aluminum atoms from EMC-2 zeolite while simultaneously replacing the aluminum atoms with extraneous silicon atoms. This increases the SiO.sub.2 /Al.sub.2 O.sub.3 ratio versus the starting EMC-2 zeolite and results in the LZ-281 zeolite having increased thermal stability, increased number and/or strength of acid sites and increased activity in hydrocarbon processes requiring strong acid sites.

Abstract: This invention relates to a novel zeolite which has the crystal structure of zeolite beta. The novel zeolite SN-beta has a unique infrared absorbance spectrum, shows enhanced activity for transalkylation of di-isopropyl-benzene and shows less deactivation for cumene synthesis. The zeolite beta is prepared by taking an as-synthesized zeolite beta, steam treating it and then ammonium ion treating it to give a zeolite SN-beta with enhanced catalytic properties.

Abstract: Useful catalyst compositions are produced by treating substituted molecular sieves with reactive titanium compounds such as titanium tetrahalides, preferably in the vapor phase at elevated temperatures. The molecular sieve starting materials contain tellurium, boron or germanium oxides in addition to silicon and titanium oxides. Olefins are efficiently transformed to epoxides using these catalyst compositions and an oxidizing agent such as hydrogen peroxide or an organic hydroperoxide.

Abstract: A method of fixation of hazardous waste materials is disclosed wherein the hazardous waste is admixed with materials capable of reacting in situ to form zeolites and the mixture subjected to conditions sufficient to form zeolites in which the hazardous material is part of the zeolite structure. The invention also relates to the resultant synthetic zeolite and to products formed by embedding the synthetic zeolites in a modified sulfur cement.

Abstract: A new family of stannosilicate molecular sieves which have the zeolite beta structure are disclosed. These molecular sieves have a three dimensional framework structure composed of at least SnO.sub.2 and SiO.sub.2 tetrahedral oxide units (and optionally TiO.sub.2 and GeO.sub.2 units) and have an empirical formula of:(Sn.sub.x Ti.sub.y Si.sub.1-x-y-z Ge.sub.z)O.sub.2where "x", "y" and "z" are the mole fractions of tin, titanium and germanium respectively. A process for preparing these molecular sieves is also presented along with processes for the selective oxidation of organic compounds with peroxides using the molecular sieves as catalysts.

Abstract: Titanium-containing zeolites containing the MEL crystal structure are prepared using an organic templating agent comprising 3,5-dimethylpiperidinium compounds. The zeolites can be made in the pure phase form, and are useful as catalysts for the oxidation of hydrocarbons.

Abstract: The present invention relates to a dealuminated IM-5 zeolite and to any catalyst comprising that zeolite which is at least partially in its acid form. The invention also relates to the preparation of the catalyst and to the catalyst. Finally, the invention relates to the use of the zeolite in a hydrocarbon conversion process.

Abstract: The present invention relates to new crystalline zeolite SSZ-43 prepared using a substituted piperidinium or decahydroquinolinium cation templating agent.

Abstract: A titanium-containing porous silica having a molecular sieve framework in which more than 3 mole % but not more than 25 mole % of silicon ions are isomorphously substituted by titanium ions. The porous silica may be obtained by gradually adding a liquid containing water and an alkylamine to a mixture containing a silicon alkoxide and a titanium alkoxide with stirring to hydrolyze the silicon alkoxide and the titanium alkoxide and to obtain a gel. The gel is then dried and calcined to obtain the titanium-containing porous silica.

Abstract: The present invention relates to a composition and a method for producing hexagonally-packed mesoporous metal oxides wherein the metal oxide is selected from transition metals and lanthanide metals. The composition includes hexagonally packed metal oxide mesostructures that are resistant to pore collapse upon removal of surfactant and are thermally stable. The composition can include a surfactant complexed with the metal. Also described are methods for producing the hexagonally-packed mesoporous metal oxides. The present invention also relates to compositions and methods for producing porous metal oxides. The compositions include microporous and mesoporous metal oxides that are resistant to pore collapse upon removal of surfactant and are thermally stable. Also described are methods for producing microporous metal oxides.

Abstract: Noncrystalline mesoporous molecular sieve substances are prepared using alkyltrimethylammonium halide as a surfactant in combination with water-soluble organic or inorganic salts capable of binding to a monovalent cation. The sieve substances are superior to the M41S series in thermal stability and hydrothermal stability. The sieve substances are structurized in such a manner that channels uniform in diameter are randomly arranged interconnecting with one another in a three-dimensional way so as to allow reactants to readily diffuse therein.

Abstract: The present invention relates to new crystalline zeolite SSZ-39 prepared using a cyclic or polycyclic quaternary ammonium cation templating agent.

Abstract: The present invention discloses a phosphorus-containing zeolite having MFI type structure. The anhydrous composition (based on the mole ratios of oxides) of the above zeolite is0.01-0.3Na.sub.2 O.Al.sub.2 O.sub.3.0.2-1.5P.sub.2 O.sub.5.30-90SiO.sub.2Said zeolite possesses a X-ray diffraction pattern listed in Table 1. The pore volume ratio of 1.0-10 nm mesopore to 10-membered ring pore is no less than 0.5. The crystal particle size of said zeolite is in the range of 0.8-2.0 micron. Said zeolite exhibits superior hydrothermal stability in catalytic conversion of hydrocarbons. Especially, when said zeolite is applied in catalytic cracking of hydrocarbons, it will enhance the crackability of large molecules, improve gasoline octane value and stability, and reduce the sulfur content in the gasoline as well.

Abstract: Mesoporous molecular sieve substances having a structure exhibiting a hexagonal arrangement of straight channels uniform in diameter, superior over MCM-41 substances of Mobil Co. in thermal stability and hydrothermal stability, can be prepared by the methods characterized in using various organic or inorganic salts.

Abstract: The present invention relates to new crystalline zeolite SSZ-36 prepared using a cyclic or polycyclic quaternary ammonium cation templating agent.

Abstract: A novel molecular sieve is disclosed which has a crystal structure which is an intergrowth of the pharmacosiderite and sitinakite structures. The molecular sieve has an empirical formula of:A.sub.((4-4x)/n) (M.sub.x Ti.sub.1-z Ge.sub.y).sub.4 (Ge.sub.1-p Si.sub.p).sub.q O.sub.rwhere A is a cation such as sodium or potassium and M is a metal such as niobium or tantalum. A process for preparing the molecular sieve is also disclosed.

Abstract: A method for modifying a crystalline molecular sieve material is provided. The crystalline molecular sieve material is modified by functionalizing it and concurrently removing its templating surfactant. The method is accomplished by contacting the crystalline molecular sieve material with a treatment composition including a functionalizing agent, an exchanging moiety and a solvent.

Abstract: The invention relates to zeolites which have high substitution levels of element with regard to aluminium content and in particular such zeolites where the substitute to silicon ratio is also high. A method for producing such zeolites by presenting the substitute material in tetrahedral oxo-anion form is also provided.

Abstract: Microporous and mesoporous metal silicates are prepared by the hydrothermal reaction of a silicon and metal source in the presence of a template. The choice of raw materials influences the purity and hence the catalytic activity of the products. A pyrogenic mixed oxide is used as the silicon and metal source. Prepared products have the composition (SiO.sub.2).sub.1-x (A.sub.m O.sub.n).sub.x, where A is Ti, Al, B, V or Zr and x is 0.005 to 0.1. Shaped objects of the microporous and mesoporous metal silicates are obtained directly by using a shaped object of the pyrogenic mixed oxide. The products obtained are used as oxidation catalysts.

Abstract: A new family of crystalline molecular sieves have been synthesized. These compositions have a microporous structure of ZrO.sub.3 octahedral units, and at least one of SiO.sub.2 tetrahedral units and GeO.sub.2 tetrahedral units. Optionally, the molecular sieves contain M metals such as titanium, niobium, or tin. These novel molecular sieves are prepared hydrothermally from a reaction mixture composed of reactive sources of the components. Additionally, these molecular sieves are useful for the selective adsorption of ammonium ions.

Abstract: A synthetic, crystalline, porous material is disclosed, together with the related preparation process. Such material of zeolitic nature containing oxides of silicon, titanium and gallium corresponds, in the calcined and anhydrous state, to the following empyrical formula:pHGaO.sub.2.qTiO.sub.2.SiO.sub.2,wherein p has a value greater than zero and smaller than or equal to 0.050, and q has a value greater than zero and smaller than or equal to 0.025, and the H.sup.+ of HGaO.sub.2 can be at least partially replaceable or replaced by cations.

Abstract: A new family of crystalline molecular sieves have been synthesized. These compositions have a microporous structure of at least ZrO.sub.3 octahedral units and SiO.sub.2 tetrahedral units. Optionally, the molecular sieves contain M metals such as titanium or tin. These novel molecular sieves are prepared hydrothermally from a reaction mixture composed of reactive sources of the components. Additionally, these molecular sieves are useful for the selective adsorption of ammonium ions.

Abstract: A novel crystalline titanium silicate designated ETS-14 molecular sieve is disclosed and characterized. ETS-14 may be prepared by heating ETS-10 molecular sieve in the form of an aqueous gel or incorporating crystals of ETS-10 with an aqueous source of sodium that is essentially free from potassium.

Abstract: Y zeolites with an SiO.sub.2 /Al.sub.2 O.sub.3 ratio in the framework of>100 with a high hydrothermal stability and resistance to aqueous, alkaline solutions are produced by treating a Y zeolite with a SiO.sub.2 /Al.sub.2 O.sub.3 ratio between 8 and 50, partially dealuminized according to known methods from NaY zeolite by treatment with silicon tetrachloride, with water vapor at temperatures between 500.degree. C. and 1000.degree. C.

Abstract: Zeolite SSZ-33 containing titanium in its framework is prepared by post-synthesis treatment with titanium tetrachloride. The titanium-containing SSZ-33 is useful as a catalyst in oxidation reactions.

Abstract: A rare earth-containing zeolite with a cocrystalline structure of ZSM-5 and ZSM-11, wherein the weight ratio of the moiety having the crystalline structure of ZSM-5 to the moiety having the crystalline structure of ZSM-11 is 0.1 to 10, which has, in the sodium form, the X-ray diffraction pattern set forth in Table 1, and in its originally synthesized anhydrous state, a chemical formula in terms of mole ratios of oxides as follows: 0.1-1.0 Na.sub.2 O.0.01-1.0 RE.sub.2 O.sub.3.Al.sub.2 O.sub.3.20-300 SiO.sub.2. Said zeolite has good acid hydrothermal stability and resistance against impurity contamination, and is useful as catalyst in various hydrocarbon conversions.

Abstract: The invention relates to a synthetic crystalline material and its use in catalytic conversion of organic compounds and as a sorbent. The crystalline material contains one or more microporous crystalline phases, having a micropore volume greater than or equal to about 0.15 cc/g distributed in channels between about 3 to about 15 .ANG. in average diameter which is rendered accessible by a mesopore volume of greater than or equal to about 0.1 cc/g distributed in channels between about 20 to about 100 .ANG. in average diameter. A process is also provided for preparing the crystalline material of the present invention.

Abstract: A high silica zeolite (UTD-1) using bis(pentamethyl-cyclopentadienyl)cobalt(III) hydroxide, Cp*.sub.2 CoOH is disclosed. UTD-1 is a large pore molecular sieve having one dimensional channels running in parallel. The synthesis and characterization of silicates incorporating titanium, vanadium, aluminum or boron in the silicate framework is described. Calcined Ti-UTD-1 containing cobalt oxide and the cobalt free molecular sieves are shown to be effective oxidation catalysts. Oxidation of alkanes with hydrogen peroxide and t-butylhydroperoxide (t-BHP) and the room temperature oxidation of cyclohexane to adipic acid are demonstrated.

Abstract: This invention relates to dimetal sulfide or selenide microporous crystalline compositions. These compositions have the empirical formulaR.sub.x (M.sup.1+.sub.y M.sup.2+.sub.z M.sub.4)A.sub.qwhere R is a cation such as tetramethylammonium ion, M.sup.1+ is a metal such as copper, silver, etc. M.sup.2+ is a metal such as zinc, cobalt, etc., M is germanium or tin and A is sulfur or selenium. The subscripts x, y, z and q represent the mole fractions of R, M.sup.1+, M.sup.2+ and A respectively. Finally, the three dimensional structure of said composition is characterized in that it contains M.sup.1+ --M.sup.1+ metal-metal bonds.

Abstract: A method for the preparation of new quasi-crystalline, porous inorganic oxide compositions formed in the presence of fluoride ion possessing a disordered assembly of worm-like channels. The method uses an interaction between various nonionic polyethylene oxide based surfactants (N.degree.) and neutral inorganic oxide precursors (I.degree.) in an aqueous solution and then the formation of dispersed particles in the aqueous solution in the presence of fluoride. This (N.degree. I.degree. F.sup.-) templating approach introduces several new concepts to mesostructure synthesis. The application of the low-cost, non-toxic and biodegradable surfactants and ambient reaction temperatures, introduces environmentally clean synthetic techniques to the formation of mesostructures. Recovery of the template can be achieved through solvent extraction where the solvent may be water or ethanol.

Abstract: An oxygen scavenging composition composed of a carrier material and a metal-loaded cationic exchange material having the metal in a zero valence state. The composition is contained within the interior cavity of a container to scavenge oxygen therein. The composition may form at least a part of the interior surface of the container or be present therein in the form of a film, mat, sachet or ceramic.

Abstract: A method is disclosed for preparing crystalline aluminosilicate zeolite L from a reaction mixture containing only sufficient water to produce zeolite L. In one embodiment, the reaction mixture is self-supporting and may be shaped if desired. In the method, the reaction mixture is heated at crystallization conditions and in the absence of an added external liquid phase, so that excess liquid need not be removed from the crystallized product prior to drying the crystals.

Abstract: This invention relates to new crystalline organic compositions having unique combinations of framework-confined uniform mesopores and textural mesopores and to a method for their preparation. The compositions typically possess a framework wall thickness of at least about 17.ANG., small elementary particle size of less than about 400.ANG., and ratio of textural to framework-confined mesoporosity of greater than about 0.2. The formation of the mesoporous structure is accomplished by a novel self-assembly mechanism involving hydrogen bonding between neutral amine surfactant (S.degree.) and neutral inorganic oxide precursor (I.degree.). This S.degree.I.degree. templating approach allows for facile and environmentally benign recycling of the cost-intensive template by simple solvent extraction methods.

Abstract: A method is disclosed for preparing crystalline aluminosilicate Y zeolite from a reaction mixture containing only sufficient water to produce Y zeolite. In one embodiment, the reaction mixture is self-supporting and may be shaped if desired. In the method, the reaction mixture is heated at crystallization conditions and in the absence of an added external liquid phase, so that excess liquid need not be removed from the crystallized product prior to drying the crystals.

Abstract: The invention relates to a luminescent zeolite of the Faujasite type containing Ce.sup.3+ ions. Such a zeolite can for instance be used in the luminescent screen of a low pressure mercury discharge lamp for use in photochemical processes. According to the invention the zeolite further contains cations S.sup.n+, wherein n.gtoreq.2 and the sum of the amount of Ce.sup.3+ ions and the amount of cations S.sup.n+ per unit cell of the zeolite is at least 16. The zeolite exhibits a high quantum efficiency for converting UV radiation of 254 nm into radiation having an emission maximum between 315 and 400 nm, even in case the Ce.sup.3+ ion content is relatively low.

Abstract: There are disclosed a fibrous zeolite ZSM-5 and a preparation method thereof. The fibrous zeolite ZSM-5 which is represented by xSiO.sub.2 (1-x)Al.sub.2 O.sub.3 (x is 0.9429.about.0.9943) can be directly used as a reinforcement material because of its fibrous form, and has sufficient sites on which other substances can be easily adsorbed and from which the adsorbed substances can be easily desorbed. Also, the fibrous zeolite can be applied to an optical material due to its transparent property.

Abstract: The present invention relates to new crystalline zeolite SSZ-42 prepared by processes for preparing crystalline molecular sieves, particularly large pore zeolites, using an organic templating agent selected from the group consisting of N-benzyl-1,4-diazabicyclo?2.2.2!octane cations and N-benzyl-1-azabicyclo?2.2.2!octane cations.

Abstract: Essentially mesoporous titanium oxide materials, having an average pore diameter of no more than about 100 .ANG. (e.g., from about 20 .ANG. to about 50 .ANG.) and an average surface area of no less than about 300 m.sup.2 /gm, preferably no less than about 500 m.sup.2 /gm are disclosed which optionally can contain an effective amount of at least one transition metal (e.g., a rare earth metal, iron, or the like) for stabilization. These materials can be formed by treating a titanium source, which is derived from a titanium alkoxide, in an organic-aqueous solution, with an organic structure directing agent (e.g., higher alkyl amine, optionally in the presence of an alcohol cosolvent) to form meso-sized micelles and hydrothermally treating the resulting composition.

Abstract: A method is disclosed for preparing crystalline aluminosilicate Y-type faujasite from a reaction mixture containing an organic template capable of producing Y-type faujasite. The reaction mixture contains only sufficient water to produce Y-type faujasite. In one embodiment, the reaction mixture is self-supporting and may be shaped if desired. In the method, the reaction mixture is heated at crystallization conditions and in the absence of an added external liquid phase, so that excess liquid need not be removed from the crystallized product prior to drying the crystals.

Abstract: The present invention disclosed a crystalline aluminosilicate which has the following characteristics:(A) an SiO.sub.2 /Al.sub.2 O.sub.3 molar ratio as determined by chemical analysis of from 5 to 11;(B) a unit cell dimension of from 24.45 to 24.55(C) a molar ratio of the Al contained in the zeolite framework to the total A1 contained in the aluminosilicate of from 0.3 to 0.9 calculated by the equations specified in the specification;(D) an alkali metal content, in terms of oxide, of from 0.02 to 1.5% by weight;(E) an X-ray diffraction pattern having peaks characteristic of zeolite Y; and(F) an ignition loss of from 0.5 to 20% by weight; anda process for producing the same, and a catalyst employing the same for the catalytic cracking of a hydrocarbon oil and the said catalyst which contains at least one metal selected from rare earth metals and alkaline earth metals.