Abstract: Provided are a release resistant moisture absorbent being environment-friendly and having excellent moisture absorbency and release resistance, and a moisture absorbent product comprising the same. The release resistant moisture absorbent of the present invention has an excellent moisture absorption rate, and also excellent release resistance in a high temperature and low humidity condition which is a driving environment of an automobile lamp, and thus, may be usefully used for an automobile lamp.

Abstract: The invention provides electro-catalyst compositions for an anode electrode of an acid mediated proton exchange membrane-based water electrolysis system. The compositions include a noble metal component selected from the group consisting of iridium oxide, ruthenium oxide, rhenium oxide and mixtures thereof, and a non-noble metal component selected from the group consisting of tantalum oxide, tin oxide, niobium oxide, titanium oxide, tungsten oxide, molybdenum oxide, yttrium oxide, scandium oxide, cooper oxide, zirconium oxide, nickel oxide and mixtures thereof. Further, the non-noble metal component can include a dopant. The dopant can be at least one element selected from Groups III, V, VI and VII of the Periodic Table. The compositions can be prepared using any solution based methods involving a surfactant approach or a sol gel approach. Further, the compositions are prepared using noble metal and non-noble metal precursors.

Abstract: The present invention provides a method for preparing a rare earth permanent magnet material. The preparation method of the present invention comprises atomizing spray process and infiltrating process, wherein the atomizing-sprayed sintered rare earth magnet is placed in a closed container before infiltrating. Through the atomizing spray process a solution containing a heavy rare earth element is coated on the surface of a sintered R1-Fe(Co)—B-A-X-M rare earth magnet, and after baking, heat treatment is performed to infiltrate the sprayed heavy rare earth element to the grain boundary phase of the sintered rare earth magnet. This method decreases the amount of a heavy rare earth element used, increases the coercive force of magnets with a little decrease of remanence, decreases the remanence temperature coefficient and coercive force temperature coefficient of the magnet, and improves resistance of the magnet against demagnetization at a high temperature.

Abstract: The present disclosure relates to a material preferably used in a guard bed, and having an increased capacity to adsorb catalyst poisons, as measured by collidine update at 200° C. The material is made by a method in which it is treated by being dried with a drying gas, preferably, at a temperature greater than about 200° C. The treated material may be used to remove impurities from untreated feed streams to, for example, aromatic alkylation and transalkylation processes, where such impurities act as catalyst poisons that cause deactivation of the acidic molecular sieve-based catalysts used, thereby increasing the cycle length of such catalysts.

Abstract: A silver impregnation solution comprising: (i) silver ions, (ii) a silver concentration enhancer selected from at least one ammonium salt having an anionic component that is thermally decomposable; or at least one amino acid, or a combination thereof, (iii) at least one organic amine; and (iv) water; wherein said components (i)-(iii) are dissolved in said impregnation solution, and oxalic acid may or may not be included. The silver impregnation solution can achieve significantly higher silver concentrations, including at least or above 33, 34, or 35 wt %. Methods for producing a silver catalyst by silver impregnation of a refractory support followed by calcination are also described. The resulting silver catalysts possess high silver loadings of typically at least 17, 18, or 19 wt %.

Abstract: A process for producing absorbent materials includes reducing a banana tree stalk into separated fibers, pressing the separated fibers to generate pressed fibers having less than 50% moisture content by weight, reducing moisture content of the pressed fibers by applying infrared heating to produce pre-dried fibers, and applying a non-thermal drying process to generate dried fibers having less than 10% moisture content by weight for employment in an absorbent material that absorbs hydrocarbons.

Abstract: The present invention provides a method for manufacturing an electro-catalytic honeycomb for controlling exhaust emissions, comprising steps of: providing a honeycomb structural frame including an outer surface, a plurality of airflow channels and a plurality of partition walls, and contacting the outer surface of the honeycomb structural frame with a molten metal to attach the molten metal in the plurality of partition walls to form a reducing environment. Accordingly, through the reducing environment in the partition wall and the oxidizing environment of a lean-burn exhaust contacted by a cathode, the electro-catalytic honeycomb generates an electromotive force between the partition wall and the cathode to drive the nitrogen oxides in the lean-burn exhaust to decompose at the cathode in order to control exhaust emissions.

Abstract: The oxide-containing particles (transition metal oxide-containing cerium dioxide particle) exert a catalyst performance, and include at least an iron oxide containing an iron component and a manganese oxide containing a manganese component on a surface of each of cerium dioxide particles, wherein the iron oxide and manganese oxide have smaller particle diameters than that of the cerium dioxide particles, and the content rate of the iron oxide and the manganese oxide is within the range of from 15.0% by mass to 35.0% by mass.

Abstract: Method for the preparation of a honeycomb catalyst including the steps of pre-coating a non-woven fibrous sheet, corrugating the fibrous sheet and rolling-up or stacking-up the corrugated sheet to form a honeycomb body. The honeycomb body is subsequently washcoated, including the addition of at least one catalytically active compound.

Abstract: A honeycomb structure is formed of a porous ceramic material and has pores in the structural body, wherein cerium dioxide is present in a state that it is incorporated in the structural body in the ceramic material, and at least a part of cerium dioxide particles is exposed on pore surfaces of the pores. The ceramic material includes cordierite or silicon carbide as a major component, the ratio of the cerium dioxide to the ceramic material is in the range of from 1.0% by mass to 10.0% by mass, and at least a part of catalyst particulates of a platinum group element such as platinum or palladium is loaded by the cerium dioxide particles.

Abstract: A honeycomb core for carrying a catalyst includes a flat metal foil and a corrugated metal foil, which are layered. The corrugated foil is configured by repeating a concavo-convex shaped part including a first top surface that is in contact with one of the flat foils, a second top surface that is in contact with another flat foil and is disposed at a position where the second top surface avoids the first top surface, and an inclined leg surface that has one end connected to the first top surface through a first bent part and another end connected to the second top surface through a second bent part, and extends in a direction inclined with respect to the first top surface and the second top surface, and has an offset part having different wave phases between front and rear in an axial direction of the honeycomb core.

Abstract: An object of at least one embodiment of the present invention is to suppress poisoning due to phosphorus derived from engine oil, and effectively purify NOx discharged from the time of engine start up to a high load condition. In an exhaust gas purification catalyst for an internal combustion engine, a catalyst layer includes: a first catalyst layer exposed to an exhaust gas flow; and a second catalyst layer formed between the first catalyst layer and the substrate. A second catalyst upstream layer formed on an upstream side of the second catalyst layer with respect to the exhaust gas flow and a first catalyst downstream layer formed on a downstream side of the first catalyst layer with respect to the exhaust gas flow include at least one of palladium and platinum, as well as an oxygen storage material as the catalyst component. An amount of the oxygen storage material in the first catalyst downstream layer is larger than an amount of the oxygen storage material in the second catalyst upstream layer.

Abstract: A exhaust gas purification apparatus is provided with; a substrate having a wall-flow structure and including entry-side cells, exit-side cells, and a porous partition; a first catalyst region formed in small diameter pores having relatively small pore diameters among internal pores in the partition; and a second catalyst region formed in large diameter pores having relatively large pore diameters among the internal pores in the partition. The first catalyst region contains a support and any one or two species of precious metal selected from Pt, Pd, and Rh loaded on the support, while the second catalyst region contains a support and any one or two species of precious metal selected from Pt, Pd, and Rh loaded on the support and other than at least the precious metal present in the first catalyst region.

Abstract: Catalyst articles having an ammonia slip catalyst (ASC) comprising a blend of platinum on a support with low ammonia storage and a first SCR catalyst, and a second catalyst, such as a diesel oxidation catalyst, a diesel exotherm catalyst (DEC), a NOx absorber, a selective catalytic reduction/passive NOx adsorber (SCR/PNA), a cold-start catalyst (CSC) or a three-way catalyst (TWC) are disclosed. The catalyst articles can also contain one or two additional SCR catalysts. The catalysts can be present in one of various configurations. The catalytic articles are useful for selective catalytic reduction (SCR) of NOx in exhaust gases and in reducing the amount of ammonia slip. Methods of using the catalytic articles in an SCR process, where the amount of ammonia slip is reduced, are also described.

Abstract: An object of the present invention is to provide a water absorbent resin which attains high liquid permeability and water absorbing speed, and which does not have problems of coloring and odor. The water absorbent resin includes: (A) a water absorbent resin particle having a carboxyl group; (B) a covalent surface crosslinking agent in which the number of carbons is not more than 10; (C) 0.001 mass % to 0.2 mass % of a water-soluble or water-dispersible polymer whose Log P is not less than 1.0; and (D) 0.001 mass % to 1 mass % of a water-soluble polyvalent cation. The water absorbent resin has not less than 20 g/g of a fixed height absorption (FHA) at a height of 20 cm.

Abstract: A monolithic catalyst, including cobalt, a metal matrix, a molecular sieve membrane, and an additive. The metal matrix is silver, gold, copper, platinum, titanium, molybdenum, iron, tin, or an alloy thereof. The molecular sieve membrane is mesoporous silica SBA-16 which is disposed on the surface of the metal matrix and is a carrier of the active component and the additive. The thickness of the carrier is between 26 and 67 ?m. The additive is lanthanum, zirconium, cerium, rhodium, platinum, rhenium, ruthenium, titanium, magnesium, calcium, strontium, or a mixture thereof. A method for preparing the monolithic catalyst is also provided.

Abstract: A lean NOx trap (LNT) catalyst includes a plurality of carriers connected to each other in series, wherein each of the carriers is embedded with at least one of a first wash coat containing magnesium (Mg)-substituted alumina, ceria (CeO2), barium (Ba), and a precious metal, a second wash coat containing magnesium (Mg)-substituted alumina, ceria (CeO2), barium (Ba), a third wash coat containing magnesium (Mg)-substituted alumina, ceria (CeO2), and a fourth wash coat containing magnesium (Mg)-substituted alumina, ceria (CeO2), and a higher content of a precious metal than the first wash coat, a ratio of the magnesium-substituted alumina to ceria (CeO2) being lower than that of the third wash coat, wherein the third and first wash coats are disposed in a foremost carrier through which exhaust gas passes sequentially from a front portion of the foremost carrier.

Abstract: A paste for manufacturing a photocatalyst is provided. The paste for manufacturing the photocatalyst includes an alcohol paste and a photocatalyst precursor. The photocatalyst precursor is dispersed in the alcohol paste, and the photocatalyst precursor includes a first metal precursor and a second metal precursor, wherein the first metal in the first metal precursor includes Zn, Sn, Cu, Fe, Mn, Ni, Co or Ag, and the second metal in the second metal precursor includes Fe.

Abstract: The present disclosure provides a multi-metallic catalyst system comprising at least one support, and at least one promoter component and an active component comprising at least two metals uniformly dispersed on the support. The present disclosure also provides a process for preparing the multi-metallic catalyst system. Further, the present disclosure provides a process for preparing upgraded fuel from biomass. The process is carried out in two steps. In the first step, a biomass slurry is prepared and is heated in the presence of hydrogen and a multi-metallic catalyst that comprises at least one support, at least one promoter component, and an active component comprising at least two metals to obtain crude biofuel as an intermediate product. The intermediate product obtained in the first step is then cooled and filtered to obtain a filtered intermediate product. In the second step, the filtered intermediate product is hydrogenated in the presence of the multi-metallic catalyst to obtain the upgraded fuel.

Abstract: Provided is an exhaust gas purifying catalyst with an excellent effect of suppressing deterioration due to aggregation of a noble metal catalyst that would occur during endurance at a high temperature. The exhaust gas purifying catalyst includes a porous support and a noble metal catalyst carried on the porous support. The porous support contains particles of an alumina-ceria-zirconia composite oxide, and the porous support has the following physical property values after subjected to baking at 900° C. for 5 hours: a pore diameter of the particles in the range of 2 to 20 nm, a specific surface area of the particles in the range of 75 to 115 m2/g, a crystallite size of a ceria-zirconia composite oxide that is contained in the particles in the range of 4 to 6 nm, and a bulk density of the particles in the range of 0.5 to 0.9 cm3/g.