子分类：
| 序号 | 专利名 | 申请号 | 申请日 | 公开（公告）号 | 公开（公告）日 | 发明人 |
|---|---|---|---|---|---|---|
| 161 | Linker exchange in zeolitic imidazolate frameworks | US13838820 | 2013-03-15 | US08920541B2 | 2014-12-30 | Zheng Ni; Mobae Afeworki; Simon Christopher Weston; John Zengel; David Lawrence Stern |
| A method is provided for replacing at least a portion of the organic linker content of a zeolitic imidazolate framework composition. The method comprises exchanging the organic linker with another organic linker. Also provided is a new material, designated as EMM-19, and a method of using EMM-19 to adsorb gases, such as carbon dioxide. | ||||||
| 162 | EMM19 novel zeolitic imidazolate framework material, methods for making same, and uses thereof | US13839720 | 2013-03-15 | US08907102B2 | 2014-12-09 | Simon Christopher Weston; Mobae Afeworki; Zheng Ni; John Zengel; David Lawrence Stern |
| A method is provided for forming a zeolitic imidazolate framework composition using at least one reactant that is relatively insoluble in the reaction medium. Also provided herein is a material made according to the method, designated as EMM-19, and a method of using EMM-19 to adsorb gases, such as carbon dioxide. | ||||||
| 163 | WOOD MATERIAL PRODUCT AND METHOD FOR THE PRODUCTION THEREOF | US14284729 | 2014-05-22 | US20140256859A1 | 2014-09-11 | Jan Gunschera; Volker Thole; Doreen Markewitz; Katrin Bokelmann; Thangaraj Selvam; Annett Halbhuber |
| The invention relates to a wood material product and a method for producing wood material products from particles containing lignocellulose and adhesives containing formaldehydes, which are intermixed and fed to a forming process after mixing. A zeolite is added to the mixture of adhesives and particles containing lignocellulose. | ||||||
| 164 | Functionalized and Multifunctional Composite Material, Method and Applications | US14138734 | 2013-12-23 | US20140178629A1 | 2014-06-26 | Parash Kalita; Wenping Jiang |
| Open-architecture constituents, such as wood fibers, are coated with an intercalated functional material and bound together to form a solid product, such as a plank. Applications for this material include decking, fencing, and the like. The functional material is applied prior to forming the solid product, either as a coating on each fiber or inserted in a fiber or fiber cluster. As the constituents, such as fibers, wear during use of the product, the functional material is released to provide continual protection of the product, such as UV resistance and fungal resistance. | ||||||
| 165 | POROUS BIOMOLECULE-CONTAINING METAL-ORGANIC FRAMEWORKS | US14179922 | 2014-02-13 | US20140163111A1 | 2014-06-12 | NATHANIEL LOUIS ROSI; JIHYUN AN |
| The invention relates to compositions including porous biomolecule-containing metal-organic frameworks and methods for their preparation. The porous biomolecule-containing metal-organic frameworks can include a metal component and a biomolecule component. The pores located within the frameworks have a pore space and said pore space is capable to adsorb materials therein. These compositions of the invention are useful in a wide variety of applications, such as, but not limited to, hydrogen and carbon dioxide sequestration, separation and storage; carbon dioxide uptake; and drug storage and release. | ||||||
| 166 | MICROPOROUS ZIRCONIUM SILICATE FOR THE TREATMENT OF HYPERKALEMIA IN HYPERCALCEMIC PATIENTS AND IMPROVED CALCIUM-CONTAINING COMPOSITIONS FOR THE TREATMENT OF HYPERKALEMIA | US13939656 | 2013-07-11 | US20140105971A1 | 2014-04-17 | Donald Jeffrey KEYSER; Alvaro F. GUILLEM |
| The present invention relates to novel calcium-containing microporous zirconium silicate compositions that are formulated to remove toxins, e.g. potassium ions, from the gastrointestinal tract at an elevated rate without removing calcium from the patient's body. Also disclosed are methods of using calcium-free or low calcium microporous zirconium silicate compositions for the treatment of hyperkalemia in patients also suffering from hypercalcemia. | ||||||
| 167 | Crystallized silicon-containing material with hierarchical and organized porosity | US12676750 | 2008-08-29 | US08623508B2 | 2014-01-07 | Alexandra Chaumonnot; Stephanie Pega; Clement Sanchez; Cedric Boissiere |
| Material with hierarchical and organized porosity in the microporosity and mesoporosity domains, consisting of at least two elementary spherical particles, each one of said particles comprising a matrix based on silicon oxide, mesostructured, having a mesopore diameter ranging between 1.5 and 30 nm and exhibiting microporous and crystallized walls of thickness ranging between 1 and 60 nm, said elementary spherical particles having a maximum diameter of 200 microns. The preparation of said material is also described. | ||||||
| 168 | MICROPOROUS ZIRCONIUM SILICATE AND ITS METHOD OF PRODUCTION | US13829415 | 2013-03-14 | US20130334122A1 | 2013-12-19 | Donald Jeffrey KEYSER; Alvaro F. GUILLEM |
| The present invention relates to novel microporous zirconium silicate compositions having a desired particle size distribution and methods of making those compositions. These compositions have an ideal particle size distribution for use ex vivo, for example in a dialysis exchange cartridge, yet retain many of the desirable properties of prior improved absorbers including high cation exchange capacity. Further, the new zirconium silicate molecular sieve absorbers can be manufactured using a technique that achieves the desired particle size distribution while eliminating the screening step that was previously necessary. | ||||||
| 169 | EMM19 NOVEL ZEOLITIC IMIDAZOLATE FRAMEWORK MATERIAL, METHODS FOR MAKING SAME, AND USES THEREOF | US13839720 | 2013-03-15 | US20130296568A1 | 2013-11-07 | Simon Christopher Weston; Mobae Afeworki; Zheng Ni; John Zengel; David Lawrence Stern |
| A method is provided for forming a zeolitic imidazolate framework composition using at least one reactant that is relatively insoluble in the reaction medium. Also provided herein is a material made according to the method, designated as EMM-19, and a method of using EMM-19 to adsorb gases, such as carbon dioxide. | ||||||
| 170 | FILM FORMED BY SECONDARY GROWTH OF SEED CRYSTALS, THREE CRYSTAL AXES OF WHICH HAD ALL BEEN UNIFORMLY ORIENTED ON SUBSTRATE | US13821813 | 2011-09-07 | US20130216772A1 | 2013-08-22 | Kyung Byung Yoon; CaoThanhTung Pham |
| The present invention provides a method for preparing a thin or thick film, comprising the steps of: (1) arranging non-spherical seed crystals on a substrate such that all the a-, b- and c-axes of each seed crystal are oriented under a predetermined rule; and (2) forming and growing the film from the seed crystals through secondary growth by exposing the arranged seed crystals of step (1) to a seed crystal growth solution. The invention also provides a film prepared by the method. According to the invention, crystals or films larger than the seed crystals can be prepared. | ||||||
| 171 | Wood Material Product and Method for the Production Thereof | US13321300 | 2010-04-30 | US20120108707A1 | 2012-05-03 | Jan Gunschera; Volker Thole; Doreen Markewitz; Katrin Bokelmann; Thangaraj Selvam; Annett Halbhuber |
| The invention relates to a wood material product and a method for producing wood material products from particles containing lignocellulose and adhesives containing formaldehydes, which are intermixed and fed to a forming process after mixing. A zeolite is added to the mixture of adhesives and particles containing lignocellulose. | ||||||
| 172 | MESOSTRUCTURED MATERIAL HAVING A HIGH ALUMINIUM CONTENT AND CONSISTING OF SPHERICAL PARTICLES OF SPECIFIC SIZE | US12935334 | 2009-02-26 | US20110111232A1 | 2011-05-12 | Alexandra Chaumonnot; Aurelie Coupe; Clement Sanchez; Cedric Boissiere; Michel Martin |
| A mesostructured material is described, which consists of at least two elementary spherical particles, each one of said particles comprising a mesostructured matrix based on aluminium oxide, said matrix having a pore diameter ranging between 1.5 and 30 nm, and an aluminium oxide content representing more than 46 wt. % of the mass of said matrix, which has amorphous walls of thickness ranging between 1 and 30 nm, said elementary spherical particles having a diameter D greater than 10 μm and less than or equal to 100 μm (10 | ||||||
| 173 | AMORPHOUS SILICON-CONTAINING MATERIAL WITH HIERARCHICAL POROSITY | US12676707 | 2008-08-18 | US20110039102A1 | 2011-02-17 | Alexandra Chaumonnot; Aurelie Coupe; Clement Sanchez; Cedric Boissiere |
| Material with hierarchical porosity consisting of at least two elementary spherical particles having a maximum diameter of 200 microns, at least one of said spherical particles comprising at least one matrix based on silicon oxide, said material having a macropore volume measured by mercury porosimetry ranging between 0.05 and 1 ml/g, a mesopore volume measured by nitrogen volumetric analysis ranging between 0.01 and 1 ml/g and a micropore volume measured by nitrogen volumetric analysis ranging between 0.03 and 0.4 ml/g, said matrix having amorphous walls. The preparation of said material is also described. | ||||||
| 174 | Method of flocculation and formulation of crystalline materials | US11453154 | 2006-06-14 | US07737316B2 | 2010-06-15 | Yun-Feng Chang; Daria N. Lissy |
| A method for determining an amount of flocculant effective to recover a molecular sieve crystalline product that comprises the steps of (a) preparing a molecular sieve crystalline product mixture; (b) separating the molecular sieve crystalline product mixture into a plurality of samples; (c) mixing at least two of the plurality of samples with a quantity of flocculant to produce a plurality of flocculated samples, wherein at least two of the plurality of flocculated samples have a different ratio of flocculant to molecular sieve crystalline product mixture; (d) measuring the viscosity or zeta potential of at least two of the plurality of flocculated samples having a different ratio of flocculant to molecular sieve crystalline product mixture; (e) establishing a relationship between the quantity of flocculant and the viscosity or zeta potential measurements; and (f) determining from the relationship the amount of flocculant effective to recover the molecular sieve crystalline product. | ||||||
| 175 | CATALYTIC MATERIALS AND METHOD FOR THE PREPARATION THEREOF | US12410262 | 2009-03-24 | US20090270245A1 | 2009-10-29 | Narendra Kumar; Marja Tiitta; Tapio Salmi; Heidi Osterholm |
| The invention is related to catalytic materials and particularly to mesoporous molecular sieves embedded with a zeolite, which are thermally stable at a temperature of at least 900° C., and to a method for the preparation of the catalytic materials. Said catalytic materials are suitable for applications in the field of hydrocarbon processing. | ||||||
| 176 | Catalytic materials and method for the preparation thereof | US11316975 | 2005-12-27 | US20060182681A1 | 2006-08-17 | Narendra Kumar; Marja Tiitta; Tapio Salmi; Heidi Osterholm |
| The invention is related to catalytic materials and particularly to mesoporous molecular sieves embedded with a zeolite, which are thermally stable at a temperature of at least 900° C., and to a method for the preparation of the catalytic materials. Said catalytic materials are suitable for applications in the field of hydrocarbon processing. | ||||||
| 177 | Mesoporous zeolitic material with microporous crystalline mesopore walls | US09728494 | 2000-11-24 | US06669924B1 | 2003-12-30 | Serge Kaliaguine; Trong On Do |
| The invention relates to a mesoporous zeolitic material having a stereoregular arrangement of uniformly-sized mesopores with diameters ranging from 20 to 500 Å and walls having a microporous nanocrystalline structure. The mesopore walls have a stereoregular arrangement of uniformly-sized micropores with diameters less than 15 Å. The mesoporous zeolite material according to the invention displays both the catalytic properties associated with zeolites containing strong Brönsted acid sites and the large mesopore surface area associated with mesoporous molecular sieves. | ||||||
| 178 | Method for making molecular sieves and novel molecular sieve compositions | US09465029 | 1999-12-16 | US06350429B1 | 2002-02-26 | Lawrence L. Murrell; Rudolf A. Overbeek; Yun-feng Chang; Nelleke Van Der Puil; Chuen Y. Yeh |
| This invention relates to the synthesis of large pore composite molecular sieves and to the synthetic large pore composite molecular sieves so produced. The molecular sieves of the invention have the same general utilities of the comparable molecular sieves of the prior art but have been found to be superior catalysts and absorbents. This invention relates to a hydrothermal synthesis of large pore molecular sieves from nutrients, at least one of which contains an amorphous framework-structure, and which framework-structure is essentially retained in the synthetic molecular sieve. This invention stems from a discovery that the intrinsic porosity characteristics of a nutrient that possesses an amorphous cation oxide-framework can be substantially retained in the final molecular sieve containing product formed by a hydrothermal process by carefully controlling the conditions under which the hydrothermal process is conducted. For example, the invention contemplates retention of the particle size in a final molecular sieve-containing product that corresponds with that of an amorphous cation oxide-framework nutrient used in its manufacture. This invention drives the selection of process conditions to achieve one or more of macro and meso porosity (“large pore composite porosity”) in the final molecular sieve product as a direct product of the hydrothermal reaction producing the molecular sieve. The invention allows the production of a molecular sieve that is in situ incorporated in the framework morphology of a solid cation oxide-framework used in the molecular sieve's manufacture. | ||||||
| 179 | Method for making molecular sieves and novel molecular sieve compositions | US939271 | 1997-09-29 | US6004527A | 1999-12-21 | Lawrence L. Murrell; Rudolf A. Overbeek; Yun-feng Chang; Nelleke Van der Puil; Chuen Y. Yeh |
| This invention relates to the synthesis of large pore composite molecular sieves and to the synthetic large pore composite molecular sieves so produced. The molecular sieves of the invention have the same general utilties of the comparable molecular sieves of the prior art but have been found to be superior catalysts and absorbents. This invention relates to a hydrothermal synthesis of large pore molecular sieves from nutrients, at least one of which contains an amorphous framework-structure, and which framework-structure is essentially retained in the synthetic molecular sieve. This invention stems from a discovery that the intrinsic porosity characteristics of a nutrient that possesses an amorphous cation oxide-framework can be substantially retained in the final molecular sieve containing product formed by a hydrothermal process by carefully controlling the conditions under which the hydrothermal process is conducted. For example, the invention contemplates retention of the particle size in a final molecular sieve-containing product that corresponds with that of an amorphous cation oxide-framework nutrient used in its manufacture. This invention drives the selection of process conditions to achieve one or more of macro and meso porosity ("large pore composite porosity") in the final molecular sieve product as a direct product of the hydrothermal reaction producing the molecular sieve. The invention allows the production of a molecular sieve that is in situ incorporated in the framework morphology of a solid cation oxide-framework used in the molecular sieve's manufacture. | ||||||
| 180 | Hydroprocessing catalyst | US734998 | 1991-07-24 | US5837639A | 1998-11-17 | Charles T. Kresge; Michael E. Leonowicz; Wieslaw J. Roth; James C. Vartuli |
| A catalytic composition comprises a metal hydrogenation- dehydrogenation component supported on a support material comprising an ultra-large pore crystalline material of high surface area and porosity. The crystalline material exhibits unusually large sorption capacity demonstrated by its benzene adsorption capacity of greater than about 15 grams benzene/100 grams at 50 torr and 25.degree. C., and has uniformly sized pores with a maximum perpendicular cross section of at least about 13 .ANG.. In a preferred form, the support material, which is preferably a metallosilicate such as an aluminosilicate, has the pores in a hexagonal arrangement, giving rise to a hexagonal electron diffraction pattern that can be indexed with a d.sub.100 value greater than about 18 .ANG.. | ||||||
QQ群二维码
意见反馈
意见反馈