Abstract: Disclosed is a catalyst for oxygen reduction and evolution reactions. The catalyst is in the form of nickel sulfide (NiS2) nanosheets. NiS2 molecules are cross-linked and oriented two-dimensionally in the NiS2 nanosheets. Also disclosed is a method for producing the catalyst.

Abstract: The present disclosure provides a method of increasing the concentration of K2O in an aqueous solution. The method comprises reacting potassium sulfate with an acidic compound to yield a product that includes potassium hydrogen sulfate. The product can be used to supplement crops in need of potassium. The product can also have other nutrients added to it, depending on the desired end use. Advantageously, these products increase yield as compared to prior art products.

Abstract: The invention proposes a novel method for the fabrication of regular arrays of MNWs using solid-state reduction (SSR). Using this method copper (Cu), silver (Ag), and palladium (Pd) nanowire (NWs) arrays were synthesized using anodic alumina membranes (AAMs) as templates. Depending on the metal loading used the NWs reached different diameters.

Abstract: An electrode material obtained using a polyol process and a synthesis method is provided. The synthesis method includes steps of preparing a mixed solution by mixing a transition metal compound, a polyacid anionic compound and a lithium compound with a polyol solvent; and obtaining a resultant product by reacting the mixed solution in a heating apparatus. There is an advantage in that the electrode material, which has crystallinity due to a structure such as an olivine structure or a nasicon structure, can be synthesized using a polyol process at a low temperature without performing a heat treatment proces. The nanoelectrode material synthesized by the method has a high crystallinity, uniform particles, and a structure having a diameter ranging from several nanometers to several micrometers. Further, the electrode material has a high electrochemical stability.

Abstract: A method for preparing a suspension of LDH particles comprises the steps of preparing LDH precipitates by coprecipitation to form a mixture of LDH precipitates and solution; separating the LDH precipitates from the solution; washing the LDH precipitates to remove residual ions; mixing the LDH precipitates with water; and subjecting the mixture of LDH particles and water from step (d) to a hydrothermal treatment step by heating to a temperature of from greater than 80° C. to 150° C. for a period of about 1 hour to about 48 hours to form a well dispersed suspension of LDH particles in water.

Abstract: A method for preparing an oil extractor is provided. The method includes dissolving 0.1˜30% by weight of a potassium sulfate, 0.1˜30% by weight of a potassium persulfate, and 0.1˜30% by weight of a manganese sulfate in a solvent to form a solution; heating the solution to synthesize a compound by a microwave; cooling a temperature of the compound to a room temperature; and removing the solvent from the compound. An extractor prepared from the method is also provided.

Abstract: A method for preparing an oil extractor is provided. The method includes dissolving 0.1˜30% by weight of a potassium sulfate, 0.1˜30% by weight of a potassium persulfate, and 0.1˜30% by weight of a manganese sulfate in a solvent to form a solution; heating the solution to synthesize a compound by a microwave; cooling a temperature of the compound to a room temperature; and removing the solvent from the compound. An extractor prepared from the method is also provided.

Abstract: Provided are embodiments of a method of synthesizing nano scale electrode materials using an ultrafast combustion technique and nano scale electrode materials synthesized using the method. The method does not require a process of annealing reaction products required for synthesis of electrode materials or any other additional processes, such as cleaning, filtering, and drying processes, so that it can take only several seconds to several minutes to obtain a resultant product.

Abstract: The invention provides a novel polyanion-based electrode active material for use in a secondary or rechargeable electrochemical cell, wherein the electrode active material is represented by the general formula AaMb(SO4)2Zd.

Abstract: The present invention is to provide an active material for a battery, which has high thermal stability and low electric potential. According to the invention, an active material for a battery comprising a M element in Group III, a Ti element, an O element, and a S element and having an M2Ti2O5S2 crystalline phase is provided to solve the problem.

Abstract: A process for producing a Group II metal sulfide phosphor precursor, comprising adding to an organic solvent an aqueous solution containing at least one of a Group II element compound, a sulfurizing agent, and a compound containing any of copper, silver, manganese, gold, and rare-earth elements to obtain a reaction mixture, heating the reaction mixture to produce an azeotrope of the water and the organic solvent, and removing water from the reaction mixture to produce a desired Group II metal sulfide in the reaction mixture, wherein the removal of water from the reaction mixture occurs by recovering only the water condensed from a vapor produced by the azeotropic distillation.

Abstract: Active materials for rechargeable batteries have a general formula Aa(MO)bM?cXO4 where A represents an alkali metal or mixture of alkali metals, a is greater than about 0.1 and less than or equal to about 2; MO is an ion containing a transition metal M not in its highest oxidation state, M? represents a metal, or mixture of metals, and b is greater than 0 and less than or equal to about 1, c is less than 1 wherein a, b and c are selected so as to maintain the electroneutrality of the compound, and X is phosphorus, arsenic, or sulfur, or mixtures thereof. Preferred active materials are alkali metal vanadyl metal phosphates of general formula Aa(VO)bM?cPO4 where a and b are both greater than 0 and c may be zero or greater. New synthetic routes are provided to alkali metal mixed metal phosphates where at least one of the starting materials is a metal-oxo group (MO)3+, where M represents a metal in a +5 oxidation state.

Abstract: A mixed metal compound for pharmaceutical use is free from aluminium and has a phosphate binding capacity of at least 30%, by weight of the total weight of phosphate present, over a pH range of from 2-8. The compound is especially useful for treatment of hyperphosphataemia. The metals are preferably iron (III) and at least one of calcium, magnesium, lanthanum and cerium. A metal sulphate for pharmaceutical use is selected from at least one of calcium, lanthanum and cerium sulphate compounds and has a phosphate binding capacity of at least 30% by weight of the total phosphate present, over a pH range from 2-8.

Abstract: A mixed metal compound for pharmaceutical use is free from aluminium and has a phosphate binding capacity of at least 30%, by weight of the total weight of phosphate present, over a pH range of from 2-8. The compound is especially useful for treatment of hyperphosphataemia. The metals are preferably iron (III) and at least one of calcium, magnesium, lanthanum and cerium. A metal sulphate for pharmaceutical use is selected from at least one of calcium, lanthanum and cerium sulphate compounds and has a phosphate binding capacity of at least 30% by weight of the total phosphate present, over a pH range from 2-8.

Abstract: Disclosed in a positive active material for a lithium secondary battery including a compound represented by formula 1 and having a 10% to 70% ratio of diffracted intensity of diffraction lines in 2?=53° (104 plane) with respect to diffracted intensity of diffraction lines in the vicinity of 2?=22° (003 plane) in X-ray diffraction patterns using a CoK?-ray, LixCoO2-yAy??(1) wherein, x is from 0.90 to 1.04, y is from 0 to 0.5, and A is selected from the group consisting of F, S and P.

Abstract: The present invention involves a process and materials for simultaneous desulfurization and water gas shift of a gaseous stream comprising contacting the gas stream with a nickel aluminate catalyst. The nickel aluminate catalyst is preferably selected from the group consisting of Ni2xAl2O2x+3, Ni(2?y)Ni0yAl2O(5?y), Ni(4?y)Ni0yAl2O(7?y), Ni(6?y)Ni0yAl2O(9?y), and intermediates thereof, wherein x?0.5 and 0.01?y?2. Preferably, x is between 1 and 3. More preferably, the nickel containing compound further comprises Ni2xAl2O2x+3?zSz wherein 0?z?2x.

Abstract: Metal vanadium oxide particles have been produced with an average diameter less than about 500 nm. The particles are produced from nanocrystalline vanadium oxide particles. Silver vanadium oxide particles, for example, can be formed by the heat treatment of a mixture of nanoscale vanadium oxide and a silver compound. Other metal vanadium oxide particles can be produced by similar processes. The metal vanadium oxide particles have very uniform properties.

Abstract: Disclosed in a positive active material for a lithium secondary battery including a compound represented by formula 1 and having a 10% to 70% ratio of diffracted intensity of diffraction lines in 2?=53° (104 plane) with respect to diffracted intensity of diffraction lines in the vicinity of 2?=22° (003 plane) in X-ray diffraction patterns using a CoK?-ray, LixCoO2-yAy??(1) wherein, x is from 0.90 to 1.04, y is from 0 to 0.5, and A is selected from the group consisting of F, S and P.

Abstract: Alunite type compound particles represented by the following general formula (I) and having a specific value of D75/D25 when D25 is the particle diameter of particles which account for 25% of the total and D75 is the particle diameter of particles which account for 75% of the total in the cumulative particle size distribution curve measured by a laser diffraction method: Ma[Al1-xM?x]3(SO42?)y(OH)z.mH2O??(I) wherein M is at least one cation selected from the group consisting of Na+, K+, NH4+ and H3O+, M? is at least one cation selected from the group consisting of Cu2+, Zn2+, Ni2+, Sn4+, Zr4+ and Ti4+, and a, m, x, y and z satisfy 0.8?a?1.35, 0?m?5, 0?x?0.4, 1.7?y?2.5, and 4?z?7, respectively. The above particles of the present invention have a small average particle diameter, are spherical, disk-like or hexagonal and have an extremely narrow particle size distribution.

Abstract: Disclosed in a positive active material for a lithium secondary battery including a compound represented by formula 1 and having a 10% to 70% ratio of diffracted intensity of diffraction lines in 2?=53° (104 plane) with respect to diffracted intensity of diffraction lines in the vicinity of 2?=22° (003 plane) in X-ray diffraction patterns using a CoK?-ray, LixCoO2-yAy??(1) wherein, x is from 0.90 to 1.04, y is from 0 to 0.5, and A is selected from the group consisting of F, S and P.

Abstract: There is provided an oxygen storage/release material using a rare earth oxysulfate or oxysulfide, which has a high oxygen storage/release capacity even at lower temperatures. The oxygen storage/release material of the present invention comprises a compound consisting of Pr2O2SO4 and/or Pr2O2S in which at least a part of Pr is replaced with Ce.

Abstract: A magnetic chemical absorbent according to the present invention is provided with a composite, which is constituted of a core substance comprising magnetite fine particles and schwertmannite being precipitated around the core substance to chemically bond therewith. This magnetic chemical absorbent can be produced in a hydrolysis reaction step, in which crystal of schwertmannite is precipitated by means of hydrolysis reaction by heating a solution of ferric salt and thereafter adding a reactive substance thereto, by means of adding magnetite fine particles into the solution after the solution is heated and before the precipitation of the crystal begins. This magnetic chemical absorbent is novel and good one whose absorption capability for harmful ion is upgraded more. In accordance with a waste-liquid treating method using this magnetic chemical substance, it is possible to intend the reduction of burdens in view of environmental and economic aspects. Moreover, this magnetic chemical absorbent is recyclable.

Abstract: Disclosed is a novel adsorbent for use in a 99Mo/99mTc generator, which is a medical diagnostic radioisotope generator, and in a 188W/188Re generator, which is a therapeutic radioisotope generator. The adsorbent composed of sulfated alumina or alumina-sulfated zirconia exhibits adsorption capacity superior to that of conventional adsorbents, and is stable and is thus loaded in a dry state in an adsorption column so that the radioisotope 99Mo or 188W can be adsorbed. Thus, it is possible to miniaturize the column, and such a miniaturized column is small, convenient to use, and highly efficient, and extracts a radioisotope satisfying the requirements for pharmaceuticals, and thus can be useful for radioisotope generators extracting 99mTc or 188Re.

Abstract: A method for the synthesis of compounds of the formula C—LixM1?yM?y(XO4)n, where C represents carbon cross-linked with the compound LixM1?yM?y(XO4)n, in which x, y and n are numbers such as 0?x?2, 0?y?0.6, and 1?n?1.5, M is a transition metal or a mixture of transition metals from the first period of the periodic table, M? is an element with fixed valency selected among Mg2+, Ca2+, Al3+, Zn2+ or a combination of these same elements and X is chosen among S, P and Si, by bringing into equilibrium, in the required proportions, the mixture of precursors, with a gaseous atmosphere, the synthesis taking place by reaction and bringing into equilibrium, in the required proportions, the mixture of the precursors, the procedure comprising at least one pyrolysis step of the carbon source compound in such a way as to obtain a compound in which the electronic conductivity measured on a sample of powder compressed at a pressure of 3750 Kg·cm?2 is greater than 10?8 S·cm?1.

Abstract: An inorganic pigment, the pigment comprising a compound which is an oxysulphide or oxyselenide of tin and a metal chosen from niobium or tantalum. The pigments are brightly colored in the color range from yellow, through orange to red, and are especially suitable for the coloration of glass and plastic substrates. Methods for the production of the pigments are also described.

Abstract: The present invention includes pure single-crystalline metal oxide and metal fluoride nanostructures, and methods of making same. These nanostructures include nanorods and nanoarrays.

Abstract: An antibacterial agent composed of silver-containing aluminum sulfate hydroxide particles represented by the following formula (X-I) or (Y-I). (AgaBb-a)bAlcAx(SO4)y(OH)z.pH2O??(X-I) [AgaBb-a]b[Ti3-cAlc](SO4)y(OH)z.pH2O??(Y-I) The above antibacterial agent of the present invention provides antibacterial molded articles and further antifungal agents, cosmetics, antibacterial paper, antibacterial deodorizing sprays and agricultural chemicals when it is mixed with a resin.

Abstract: A powder material comprising a compound which electrochemically intercalates and deintercalates a lithium ion. The powder material is comprised mainly of a compound containing at least an oxygen element, a sulfur element and at least one transition metal element.

Abstract: Disclosed is metal composite oxides having the new crystal structure. Also disclosed are ionic conductors including the metal composite oxides and electrochemical devices comprising the ionic conductors. The metal composite oxides have an ion channel formed for easy movement of ions due to crystallographic specificity resulting from the ordering of metal ion sites and metal ion defects within the unit cell. Therefore, the metal composite oxides according to the present invention are useful in an electrochemical device requiring an ionic conductor or ionic conductivity.

Abstract: A pretreatment agent for a sample to be subjected to Limulus assay comprising an alkali metal sulfate and/or an alkaline earth metal sulfate wherein the sulfate(s) has a final concentration of 20 mM or more when the sulfate(s) is allowed to contact with the sample, or an alkali metal halide and/or an alkaline earth metal halide wherein the halide(s) has a final concentration of from 0.4 M to 1.2 M or less when the halide(s) is allowed to contact with the sample, or a kit for Limulus assay reagent comprising thereof as a composing article.

Abstract: Alunite type compound particles represented by the following general formula (I) and having a specific value of D75/D25 when D25 is the particle diameter of particles which account for 25% of the total and D75 is the particle diameter of particles which account for 75% of the total in the cumulative particle size distribution curve measured by a laser diffraction method: Ma[Al1-xM?x]3(SO42?)y(OH)z.mH2O??(I) wherein M is at least one cation selected from the group consisting of Na+, K+, NH4+ and H3O+, M? is at least one cation selected from the group consisting of Cu2+, Zn2+, Ni2+, Sn4+, Zr4+ and Ti4+, and a, m, x, y and z satisfy 0.8?a?1.35, 0?m?5, 0?x?0.4, 1.7?y?2.5, and 4?z?7, respectively. The above particles of the present invention have a small average particle diameter, are spherical, disk-like or hexagonal and have an extremely narrow particle size distribution.

Abstract: A method of preparing metal chalcogenides from elemental metal or metal compounds has the following steps: providing at least one elemental metal or metal compound; providing at least one element from periodic table groups 13-15; providing at least one chalcogen; and combining and heating the chalcogen, the group 13-15 element and the metal at sufficient time and temperature to form a metal chalcogenide. A method of functionalizing the surface of semiconducting nanoparticles has the following steps: providing at least one metad compound; providing one chalcogenide having a cation selected from the group 13-15 (B, Al, Ga, In, Si, Ge, Sn, Pb, P, As, Sb and Bi); dissolving the chalcogenide in a first solution; dissolving the metal compound in a second solution; providing and dissolving a functional capping agent in at least one of the solutions of the metal compounds and chalcogenide; combining all solutions; and maintaining the combined solution at a proper temperature for an appropriate time.

Abstract: The present invention relates to a method for preparing an electroactive metal polyanion or a mixed metal polyanion comprising forming a slurry comprising a polymeric material, a solvent, a polyanion source or alkali metal polyanion source and at least one metal ion source; heating said slurry at a temperature and for a time sufficient to remove the solvent and form an essentially dried mixture; and heating said mixture at a temperature and for a time sufficient to produce an electroactive metal polyanion or electroactive mixed metal polyanion.

Abstract: A chain antimony oxide fine particle group comprising antimony oxide fine particles which have an average particle diameter of 5 to 50 nm, are connected in the form of a chain and have an average connection number of 2 to 30 and preferably used for forming a hard coating film. The fine particle group can be prepared by a process comprising treating an alkali antimonate aqueous solution with a cation exchange resin to prepare an antimonic acid (gel) dispersion and then treating the dispersion with an anion exchange resin and/or adding a base to the dispersion. Also provided is a substrate with a film comprising a substrate and a hard coating film. The hard coating film includes a chain inorganic oxide fine particle group, in which inorganic oxide fine particles of 2 to 30 on the average are connected in the form of a chain, and a matrix.

Abstract: Method of synthesis for a material made of particles having a core and a coating and/or being connected to each other by carbon cross-linking, the core of these particles containing at least one compound of formula LixM1?yM?y(XO4)n, in which x,y and n are numbers such as 0?x?2, 0?y?0.6 and 1?n?1.5, M is a transition metal, M? is an element with fixed valency, and the synthesis is carried out by reaction and bringing into equilibrium the mixture of precursors, with a reducing gaseous atmosphere, in such a way as to bring the transition metal or metals to the desired valency level, the synthesis being carried out in the presence of a source of carbon called carbon conductor, which is subjected to pyrolysis. The materials obtained have excellent electrical conductivity as well as very improved chemical activity.

Abstract: The invention relates to a composition of matter comprising at least one metal from Group 3, at least one metal from Group 4, sulfur and oxygen, particularly useful as a catalyst for ether decomposition to alkanols and alkenes.

Abstract: The present invention relates to particles or powders of a compound of formula Zn1?yMyO1?xSx, wherein x has a value in the range from 0.01 to 0.08, M represents a divalent metal and y has a value in the range from 0 to 0.2, the compound having a wurtzite structure.

Abstract: Improved solid acid electrolyte materials, methods of synthesizing such materials, and electrochemical devices incorporating such materials are provided. The stable electrolyte material comprises a solid acid in a eulytine structure capable of undergoing rotational disorder of oxyanion groups and capable of extended operation at elevated temperatures, that is, solid acids having hydrogen bonded anion groups; a superprotonic disordered phase; and capable of operating at temperatures of ˜100° C. and higher.

Abstract: The present invention provides new amorphous or partially crystalline mixed anion chalcogenide compounds for use in proton exchange membranes which are able to operate over a wide variety of temperature ranges, including in the intermediate temperature range of about 100 ° C. to 300° C., and new uses for crystalline mixed anion chalcogenide compounds in such proton exchange membranes. In one embodiment, the proton conductivity of the compounds is between about 10?8 S/cm and 10?1 S/cm within a temperature range of between about ?60 and 300° C. and a relative humidity of less than about 12%.

Abstract: A method for preparing a positive active material for a rechargeable lithium battery is provided. In this method, a lithium source, a metal source, and a doping liquid including a doping element are mixed and the mixture is heat-treated.

Abstract: Disclosed herein is a powder material comprising a compound which electrochemically intercalates and deintercalates a lithium ion, wherein the powder material is comprised mainly of a compound containing at least an oxygen element, a sulfur element and at least one transition metal element.

Abstract: A non-aluminum containing mixed metal compound for pharmaceutical use, which may, for example, be a mixed metal hydroxy carbonate containing magnesium and iron, and may have a hydrotalcite structure, preferably a non-aged hydrotalcite structure. Other metals, including, for example, calcium, lanthanum and cerium, may also be used. Metal sulphate compounds, especially calcium sulphate, lanthanum sulphate and/or cerium sulphate, compounds are also useful. The mixed metal compounds have a phosphate binding capacity of at least 30%, by weight, based on the test methods 1, 2 or 3, described in the specification, over a pH range from 3 to 7, such as from 2 to 8. The compound is especially useful in the treatment of hyperphosphataemia.

Abstract: A photocatalyst which comprises an oxysulfide containing at least one transition metal; a preferable photocatalyst which also comprises a rare earth element such as Sm in addition to the above and wherein the transition metal is at least one selected from the group consisting of Ti and Nb; a more preferable photocatalyst which further comprises a promoter comprising a transition metal such as Pt loaded on each of the above photocatalyst; and a catalyst for use in the decomposition of water by a light which comprises one of the above oxysulfide photocatalysts.

Abstract: Active materials for rechargeable batteries have a general formula

Abstract: A composite metal polybasic salt containing a trivalent metal, zinc metal and a divalent metal as metal components and having a novel crystal structure, and a method of preparing the same. The invention further deals with a composite metal polybasic salt which has anion-exchanging property, which by itself is useful as an anion-exchanger, capable of introducing anions suited for the use upon anion-exchange, and finds a wide range of applications, and a method of preparing the same. The composite metal polybasic salt has a particular chemical composition and X-ray diffraction peaks, exhibiting peaks at 2&thgr;=2 to 15°, 2&thgr;=19.5 to 24° and 2&thgr;=33 to 50°, and a single peak at 2&thgr;=60 to 64° in the X-ray diffraction (Cu-&agr;).

Abstract: A composite metal polybasic salt containing a trivalent metal, zinc metal and a divalent metal as metal components and having a novel crystal structure, and a method of preparing the same. The invention further deals with a composite metal polybasic salt which has anion-exchanging property, which by itself is useful as an anion-exchanger, capable of introducing anions suited for the use upon anion-exchange, and finds a wide range of applications, and a method of preparing the same. The composite metal polybasic salt has a particular chemical composition and X-ray diffraction peaks, exhibiting peaks at 2&thgr;=2 to 15°, 2&thgr;=19.5 to 24° and 2&thgr;=33 to 50°, and a single peak at 2&thgr;=60 to 64° in the X-ray diffraction (Cu-&agr;).

Abstract: Disclosed is a positive active material for a rechargeable lithium battery. The positive active material includes at least one compound represented by formulas 1 to 4 and a metal oxide or composite metal oxide layer formed on the compound.

Abstract: Method of synthesis for a material made of particles having a core and a coating and/or being connected to each other by carbon cross-linking, the core of these particles containing at least one compound of formula LixM1−yM′y(XO4)n, in which x,y and n are numbers such as 0≦x≦2, 0≦y≦0.6 and 1≦n≦1.5, M is a transition metal, M′ is an element with fixed valency, and the synthesis is carried out by reaction and bringing into equilibrium the mixture of precursors, with a reducing gaseous atmosphere, in such a way as to bring the transition metal or metals to the desired valency level, the synthesis being carried out in the presence of a source of carbon called carbon conductor, which is subjected to pyrolysis. The materials obtained have excellent electrical conductivity as well as very improved chemical activity.

Abstract: A cathode active material for a lithium secondary cell used in a cellular phone is disclosed. The cathode active material for the lithium secondary cell and the method the same having a high capacity and a long lifetime, different from LiCoO2 and LiMn2O4, Li(Ni, Co)O2, and V-system oxide that has been researched as the active material for substituting LiCoO2 are provided. The cathode active material for the lithium secondary cell in the next formula 1 is obtained by heating or chemically treating diadochite [Fe2(PO4)(SO4)(OH).6H2O] that is the mineral containing PO43−, SO42−, and OH−.

Abstract: A composite metal polybasic salt containing a trivalent metal and magnesium as metal components and having a novel crystal structure, and a method of preparing the same. The invention further deals with a composite metal polybasic salt which has anion-exchanging property, which by itself is useful as an anion-exchanger, capable of introducing anions suited for the use upon anion-exchange, and finds a wide range of applications, and a method of preparing the same. The composite metal polybasic salt has a particular chemical composition and X-ray diffraction peaks, and further has a degree of orientation (Io) of not smaller than 1.5.