Abstract: Provided is an arsenic-containing solid comprising 100 parts by mass of a scorodite-type iron-arsenic compound and at least 1 part by mass of an iron oxide compound added thereto, in which the scorodite-type iron-arsenic compound is produced by adding an oxidizing agent to an aqueous acidic solution that contains a 5-valent arsenic (V) ion and a 2-valent iron (II) ion, then promoting the precipitation of an iron-arsenic compound with stirring the liquid, and finishing the precipitation thereof within a range where the pH of the liquid is at most 1.2. The iron oxide compound includes goethite, hematite and their mixture, preferably having a BET specific surface area of at least 3 m2/g, more preferably at least 20 m2/g.

Abstract: The invention provides a process for producing an aqueous dispersion of particles of rutile titanium oxide, which comprises: a first step in which after a chloride ion concentration of an aqueous solution of titanium tetrachloride is adjusted to 0.5 mole/L or more and less than 4.4 mole/L, the aqueous solution of titanium tetrachloride is heated at a temperature in a range of from 25° C. to 75° C.

Abstract: A crystalline titanium dioxide containing fluorine atoms within the crystal lattice comprising atoms of titanium and oxygen is described; this titanium dioxide is particularly suitable for the production of solid-state electrolytes, hybrid membranes for fuel cells or electrolysers. The aforesaid titanium dioxide may be produced using a process comprising the following stages: (a) a titanium ore is reacted with a NH4HF2 aqueous solution; (b) the aqueous dispersion thus obtained is filtered with consequent separation of a solid residue and an aqueous solution containing titanium salts; (c) the aqueous solution thus obtained is subjected to hydrolysis, said hydrolysis comprising a first stage at pH 6.5-8.0 and a second stage at pH 9-11; (d) the aqueous dispersion thus obtained is filtered and the solid residue is subjected to pyrohydrolysis at a maximum temperature of approximately 500° C., preferably approximately 450° C.

Abstract: The present invention relates to a novel Mg—Ti—Al composite metal hydroxide and to production method therefor. Mg—Ti—Al composite hydroxide particles can be obtained by subjecting a solution containing a magnesium salt and a titanium salt to ultrasound processing and carrying out a high-temperature and high-pressure reaction with a solution containing an aluminum salt in the proportions of the metal elements comprised in the Mg—Ti—Al composite metal hydroxide, thereby giving the advantageous effects that the halogen capturing ability is excellent and, when used in a polymer, degradation and earily-staining prevention properties and transparency are outstanding.

Abstract: The method described herein allows for melt stabilization and vapor-phase synthesis of a cesium germanium halide utilizing germanium dihalides formed in situ. This disclosure allows for the melting of cesium germanium halides without decomposition, which allows for growing crystals of these materials from the melt. This disclosure allows for a direct synthesis of these materials without the use of water or the introduction of other possible contaminants.

Abstract: The invention relates to methods for creating metal oxide coatings on one or more surfaces employing a magnetic field, and articles containing those coatings. Such methods involve contacting the surfaces to be treated with a metal compound, and converting the metal compound to metal oxide for example by heating the surfaces to the desired temperature in the presence of a magnetic field. The magnetic field dramatically improves, in some embodiments, the characteristics of the metal oxide coating.

Abstract: Provided is a cathode active material for a non-aqueous electrolyte secondary battery capable of obtaining high initial discharge capacity and good output characteristics at low temperature. In order to achieve this, a cathode active material that is a lithium nickel composite oxide composed of secondary particles that are an aggregate of primary particles is expressed by the general expression: Liw(Ni1-x-yCoxAly)1-zMzO2 (where 0.98?w?1.10, 0.05?x?0.3, 0.01?y?0.1, 0?z?0.05, and M is at least one metal element selected from a group consisting of Mg, Fe, Cu, Zn and Ga), and where the crystallite diameter at (003) plane of that lithium nickel composite oxide that is found by X-ray diffraction and the Scherrer equation is within the range of 1200 {acute over (?)} to 1600 {acute over (?)} is used as the cathode material.

Abstract: A mesoporous metal oxide materials with a chiral organization; and a method for producing it, in the method a polymerizable metal oxide precursor is condensed inside the pores of chiral nematic mesoporous silica by the so-called “hard templating” method. As a specific example, mesoporous titanium dioxide is formed inside of a chiral nematic silica film templated by nanocrystalline cellulose (NCC). After removing the silica template such as by dissolving the silica in concentrated aqueous base, the resulting product is a mesoporous titania with a high surface area. These mesoporous metal oxide materials with high surface area and chiral nematic structures that lead to photonic properties may be useful for photonic applications as well as enantioselective catalysis, photocatalysis, photovoltaics, UV filters, batteries, and sensors.

Abstract: An iron composition having a plurality of elemental components is disclosed. The major component is an iron component of at least about 68% to about 92% iron by weight. Other components by weight include manganese; cerium; carbon; phosphorous; sulfur; aluminum; silicon; chromium; copper; and zinc. Combined with layers of sand, brick chips and/or charcoal, the iron composition can be used to create a water filter for filtering inorganic arsenic species and soluble metal ions out of water. To enhance hydrous ferric oxide complexation and precipitation, the iron composition may be treated with food grade acids or a water mixture.

Abstract: Disclosed herein is a recording material for an optical recording medium. The recording material has a composition represented by a general formula of BixGeyO(1-x-y), in which x and y respectively are atomic ratios of bismuth and germanium, and satisfy the requirements of the following formulae: 2.8?(x/y)?25 and 0.55?(1?x?y)?0.62.

Abstract: The production method of the present invention is a method for producing porous aluminum magnesium titanate by forming a mixture containing Al source powder, Mg source powder, Ti source powder and Si source powder as well as a pore-forming agent to obtain a molded body; presintering the obtained molded body; and then sintering the presintered molded body, wherein the content of the pore-forming agent to a total of 100 parts by mass for the Al source powder, Mg source powder, Ti source powder and Si source powder is 5 to 30 parts by mass, the melting point of the Si source powder is 600 to 1300° C., when the elemental composition ratio of Al, Mg, Ti and Si in the mixture is represented by compositional formula (1): Al2(1?x)MgxTi(1+x)O5+aAl2O3+bSiO2 ??(1), x satisfies 0.05?x?0.15, a satisfies 0?a?0.1 and b satisfies 0.05?b?0.15, and the presintered molded body is sintered at 1300 to 1560° C.

Abstract: The present disclosure relates to a novel method of preparing a vanadosilicate molecular sieve, and a vanadosilicate molecular sieve and their derivatives prepared by the same method. The preparing method of a vanadosilicate molecular sieve includes forming a vanadosilicate molecular sieve by a hydrothermal reaction of a reaction mixture containing a silicon source, a base, a V5+-containing compound as a vanadium source, a reducing agent, a salt and water.

Abstract: An iron-carbon composition including iron chemically bonded to carbon, wherein the iron and the carbon form a single phase material, characterized in that the carbon does not phase separate from the iron when the single phase material is heated to a temperature that melts the iron-carbon composition.

Abstract: A chlorinated oligogermane as a pure compound or mixture of compounds which each have at least one direct Ge—Ge bond, substituents of which include chlorine or chlorine and hydrogen and atom ratio for substituent:germanium is at least 2:1 in the composition thereof, wherein a) the mixture has on average a Ge:Cl ratio of 1:1 to 1:3, or the pure compound has a Ge:Cl ratio of 1:2 to 1:2.67, and b) the mixture has an average number of germanium atoms of 2 to 8.

Abstract: Methods for forming doped silane and/or semiconductor thin films, doped liquid phase silane compositions useful in such methods, and doped semiconductor thin films and structures. The composition is generally liquid at ambient temperatures and includes a Group IVA atom source and a dopant source. By irradiating a doped liquid silane during at least part of its deposition, a thin, substantially uniform doped oligomerized/polymerized silane film may be formed on a substrate. Such irradiation is believed to convert the doped silane film into a relatively high-molecular weight species with relatively high viscosity and relatively low volatility, typically by cross-linking, isomerization, oligomerization and/or polymerization. A film formed by the irradiation of doped liquid silanes can later be converted (generally by heating and annealing/recrystallization) into a doped, hydrogenated, amorphous silicon film or a doped, at least partially polycrystalline silicon film suitable for electronic devices.

Abstract: The present invention relates to a process for the production of phyllosilicate platelets having a high aspect ratio, to a phyllosilicate platelet obtainable by the process according to the invention, to the use of phyllosilicate platelets according to the invention in the production of a composite material, of a flameproof barrier or of a diffusion harrier, and to a composite material comprising or obtainable using phyllosilicate platelets according to the invention.

Abstract: The present invention provides a method for preparing modified micronized particles, comprising the steps of carrying out co-precipitation in an aqueous solution at a temperature between the freezing point and the boiling point of the reaction mother liquid to produce a mixed precipitate of micronized particles or precursors thereof and an inorganic precipitate. The method effectively solves the conflict between micronization and surface modification of particles, and resolves the problem that it is difficult to separate micronized particles from the reaction mother liquid.

Abstract: A solid mixture of fullerene and titanium hydride, a method of its formation, and a method of its use to rapidly produce a gaseous mixture of molecular hydrogen and fullerene on demand. The solid mixture may be resistively heated by discharge of a high power electrical current from a capacitor bank through the mixture to produce the mixture of hydrogen and fullerene within a few tens of microseconds. The resulting gaseous mixture of hydrogen and fullerene may be ionized and accelerated for the purpose of mitigating electromagnetic disruptions in a magnetically confined plasma.

Abstract: This invention pertains to method for imparting a durable antimicrobial activity to substrates, particularly textiles. An acetate-free metal and peroxide antimicrobial treatment formulation is prepared by adjusting the pH of a mixture of a metal salt in aqueous hydrogen peroxide to about 7.5. The substrate is treated with the composition and dried to afford the treated substrate with antimicrobial activity. Zinc salts, ions, or complexes are preferred.

Abstract: A method for producing nanoparticles includes: producing a nanoparticle dispersion ion gel in which a plurality of nanoparticles are dispersed; and dissolving the nanoparticle dispersion ion gel, thereby producing a liquid in which the plurality of nanoparticles are dispersed.

Abstract: This invention provides processes and systems for converting biomass into high-carbon biogenic reagents that are suitable for a variety of commercial applications. High carbon biogenic reagents are also provided.

Abstract: An embodiment of an inorganic nanocomposite includes a nanoparticle phase and a matrix phase. The nanoparticle phase includes nanoparticles that are arranged in a repeating structure. In an embodiment, the nanoparticles have a spherical or pseudo-spherical shape and are incompatible with hydrazine. In another embodiment, the nanoparticles have neither a spherical nor pseudo-spherical shape. The matrix phase lies between the nanoparticles of the nanoparticle phase. An embodiment of a method of making an inorganic nanocomposite of the present invention includes forming a nanoparticle superlattice on a substrate. The nanoparticle superlattice includes nanoparticles. Each nanoparticle has organic ligands attached to a surface of the nanoparticle. The organic ligands separate adjacent nanoparticles within the nanoparticle superlattice. The method also includes forming a solution that includes an inorganic precursor.

Abstract: Disclosed are: nickel complex hydroxide particles that have small and uniform particle diameters; and a method by which the nickel complex hydroxide particles can be produced. Specifically disclosed is a method for producing a nickel complex hydroxide by a crystallization reaction, which comprises: a nucleation step in which nucleation is carried out, while controlling an aqueous solution for nucleation containing an ammonium ion supplying material and a metal compound that contains nickel to have a pH of 12.0-13.4 at a liquid temperature of 25° C.; and a particle growth step in which nuclei are grown, while controlling an aqueous solution for particle growth containing the nuclei, which have been formed in the nucleation step, to have a pH of 10.5-12.0 at a liquid temperature of 25° C. In this connection, the pH in the particle growth step is controlled to be less than the pH in the nucleation step.

Abstract: The invetion relates to a titanium dioxide-based photocatalyst containing carbon that is highly photoactive in visible light (vlp-TiO2) and to a method of manufacture. The vlp-TiO2is manufactured by mixing a fine grained titanium compount (BET?50 m2/g) with an organic carbon compound and subsequent thermal treatment at temperatures up to 350° C. The carbon content amounts to 0.05 to 4% by weight, preferably 0.4 to 0.8% by weight. The product is characterized by an ESR spectrum which displays only one significant signal in the g value range from 1.97 to 2.05 at g about 2.003. The inventive photocatalyst can be used for to degrade contaminants and pollutants in liquids and gases.

Abstract: Provided is a precursor for the preparation of a lithium transition metal oxide that is used for the preparation of a lithium transition metal oxide as a cathode active material for a lithium secondary battery, through a reaction with a lithium-containing compound, wherein the precursor contains two or more transition metals, and sulfate ion (SO4)-containing salt ions derived from a transition metal salt for the preparation of the precursor have a content of 0.1 to 0.7% by weight, based on the total weight of the precursor.

Abstract: First, an ionic liquid is placed on a glass slide, which is then installed in an evaporation apparatus, and a metal (for example, indium) is mounted as a target material at a position facing the ionic liquid, followed by sputter deposition of the metal. After sputtering, the ionic liquid containing nanoparticles dispersed therein is recovered. The nanoparticles are solid nanoparticles. Next, the ionic liquid containing the solid nanoparticles dispersed therein is placed in a test tube and then oxidized by heating in air at 250° C. for 1 hour. As a result, hollow nanoparticles having cavities formed in core portions of the solid nanoparticles are produced.

Abstract: The invention provides a boron suboxide composite material comprising boron suboxide and a secondary phase, wherein the secondary phase contains a metal selected from the group of gold, silver and copper and alloys based on or containing one or more of these metals. Moreover, the metal or alloy is present in the material in an amount of less than about 20 volume %, and preferably less than about 6 volume %.

Abstract: Disclosed is an aqueous solution of a chromium salt, in which the oxalic acid content is 8% by weight or less relative to chromium. In the aqueous solution of the chromium salt, the total organic carbon content is 4% by weight or less relative to chromium. The chromium salt is preferably a chromium chloride, a chromium phosphate, or a chromium nitrate. The chromium chloride preferably contains a basic chromium chloride represented by the composition formula Cr(OH)xCly (wherein 0<x?2, 1?y<3, and x+y=3). The chromium phosphate is preferably one represented by the composition formula Cr(H3-3/nPO4)n (wherein n is a number satisfying 2?n?3). The chromium nitrate is preferably a basic chromium nitrate represented by the composition formula Cr(OH)x(NO3)y (wherein 0<x?2, 1?y<3, and x+y=3).

Abstract: The invention relates to a crosslinking initiator including a mineral filler and a zinc compound grafted on to said mineral filler, where said zinc compound is chosen from the group consisting of zinc oxide, zinc hydroxide and the mixtures thereof, the zinc compound being in the form of individual rod-like particles of nanometric size, and the mineral filler being in the form of grains having a particle size larger than that of the zinc compound and where the individual particles of the zinc compound are grafted on to the surface of the grains of the mineral filler in a uniformly dispersed manner.

Abstract: The present invention provides for a composition capable of storing hydrogen from molecular hydrogen. The composition comprises a magnesium nanoparticle (NP) and a polymer, wherein the Mg NC is essentially embedded in the polymer. The polymer is selectively permeable wherein the polymer is essentially not permeable to O2 and H2O. The composition is capable of absorbing and desorbing molecular hydrogen.

Abstract: A phase change material comprising a quaternary GaTeSb material consisting essentially of MA(GaxTeySbz)B, and where M comprises a group IVA element C, Si, Ge, Sn, Pb, a group VA element N, P, As, Sb, Bi, or a group VIA element O, S, Se, Te, Po, having a value A such that the transition temperature is increased relative to the transition temperature in GaxTeySbz, without M, and the difference between the melting temperature and the transition temperature is reduced relative to the difference in GaxTeySbz, without M.

Abstract: The disclosure provides processes and systems for sterilizing an object using a sterilant gas. In some embodiments, the sterilant gas is produced by the thermal decomposition of a salt. Compositions to generate sterilant gasses are also disclosed.

Abstract: The present invention relates to a process for preparing a trichloroammineplatinate salt by reacting a tetrachloroplatinate salt in aqueous solution in the presence of ammonium chloride and an alkali chloride with one or more carbonate salts selected from the group consisting of potassium, sodium and ammonium carbonate while keeping the pH value below 7 during the reaction; the product obtained therein and a use thereof.

Abstract: The present invention provides an improved method for the purification of a mixture of complexes comprising a stress protein complexed to a peptide or peptide fragment from a source mixture, typically a cell lysate. The method of the invention provides for protein complexes to be purified using ion exchange chromatography based methods, wherein a modified buffer solution is used which results in the purified stress protein complexes being more immunogenic than protein complexes obtained using conventional methodology. The purified complexes can be used to produce improved vaccine preparations which elicit enhanced immune responses in the subjects to whom the vaccine compositions are administered.

Abstract: A detoxifying agent and a detoxifying method are provided which have a high detoxifying ability in a detoxifying treatment of a discharge gas containing a volatile inorganic hydride and generating in a semiconductor production step. A zeolite is added to a solid metal hydroxide, a solid metal carbonate, a solid basic metal carbonate, or a mixture of these compounds to thereby obtain the detoxifying agent which has the excellent ability to detoxify a discharge gas containing volatile inorganic hydride. The zeolite to be added is a synthetic zeolite selected from zeolite Y, MFI zeolite, mordenite zeolite, beta zeolite, zeolite A, zeolite X, and zeolite L or is a natural zeolite.

Abstract: Neutral calcium-aluminum double salts of the formula (A): Ca2m(Zn2n)Al2(OH)6+2(2m+2n?1)An*oH2O??(A), where the following apply for m and n:m=0.5 to 3 and 0.5m?n>0; An=CO3, where this may be replaced completely or partially by at least one of the following groups selected from OH, ClO4 and H3CS(?O)2O (triflate) and o=0 to 3. The present invention further relates to their preparation, use in compositions and stabilizer systems and uses thereof.

Abstract: A sintered particle has the following chemical analysis, as percentages by weight: ZrO2 partially stabilized with CeO2 and Y2O3: complement to 100%; Al2 10%-60%; additive selected from CaO, a manganese oxide, La2O3, SrO, BaO, and mixtures thereof: 0.2%-6; the quantity of CaO being less than 2%; impurities: <2%; the zirconia being stabilized with CeO2 and Y2O3 present in quantities such that, as molar percentages based on the sum of ZrO2, CeO2 and Y2O3: CeO2: 6 mol %-11 mol %; and Y2O3: 0.5 mol %-2 mol %; the particle being obtained by sintering at a sintering temperature higher than 1300° C., the sintering temperature being higher than 1400° C. if the additive is CaO or if the molar CeO2 content is in the range 10% to 11%.

Abstract: An aluminum chelate-based latent curing agent is provided which can cure a thermosetting epoxy resin at a relatively low temperature in a short period of time. A method for producing such an aluminum chelate-based latent curing agent, whose curing conditions can be relatively easily controlled, is also provided. The aluminum chelate-based latent curing agent is made latent by reacting a silsesquioxane-type oxetane derivative with an aluminum chelating agent in the presence of an alicyclic epoxy compound.

Abstract: Shape controlled synthesis of ferroelectric nanocrystals such as barium titanate (BaTiO3) nanocrystals is described. By tuning the molar ratio between the surfactant and the metal precursors, BaTiO3 nanocrystals with different shapes are readily obtained. This provides the nanoscopic ferroelectric building blocks for the fabrication of various electronic devices, as well as for fundamental research in nanoscience and nanotechnology.

Abstract: Provided is a transition metal precursor comprising a composite transition metal compound represented by Formula 1, as a transition metal precursor used in the preparation of a lithium-transition metal composite oxide: M(OH1?x)2??(1) wherein M is two or more selected from the group consisting of Ni, Co, Mn, Al, Cu, Fe, Mg, B, Cr and the transition metals of 2 period in the Periodic Table of the Elements; and 0<x<0.5. The transition metal precursor in accordance with the present invention has an oxidation number of a transition metal approximate to an oxidation number of a transition metal of the lithium-transition metal composite oxide prepared therefrom. Therefore, when the lithium-transition metal composite oxide is prepared using such a precursor, an oxidation or reduction process for varying an oxidation number can be simplified, resulting in superior process efficiency.

Abstract: A multilayer component includes a dielectric ceramic material that can be co-sintered with a varistor ceramic to form a monolithic multilayer component according to the invention. The multilayer component therefore includes a layer of a varistor ceramic and another layer of a dielectric. Both layers can be arranged directly adjacent to one another in the multilayer component. In the multilayer component, metallizations are arranged on or between the ceramic layers. The metallizations are structured to form conductor sections and metallized areas. The metallizations form together with the ceramic layers alongside a varistor at least one further component selected from at least one of the component functions.

Abstract: A hydrogen-generating material and method for generating hydrogen are provided. A plurality of metal particles and a plurality of modifier particles are mixed and then reacted with water to generate hydrogen. The metal particles are made of material including aluminum or aluminum alloy or combination thereof. The modifier particles preferably comprise titanium dioxide (TiO2) particles, and the average particle size of the modifier particles is preferably less than 25 nm.

Abstract: The invention relates to a composition capable of trapping hydrogen comprising: (a) at least one mineral compound of formula (I) below: MX(OH)??(I) in which: M represents a divalent transition element; O represents an oxygen atom; X represents an atom chosen from S, Se, Te, Po; and H represents a hydrogen atom; and (b) at least one nitrate salt of formula (II) below: ZNO3??(II) in which Z is a monovalent cation. Use of these compositions either in pulverulent form for trapping gaseous hydrogen by direct interaction, or in the form of an adjuvant in a containment material for, for example, trapping hydrogen released by radiolysis in radioactive waste packages.

Abstract: A nanocomposite with high dielectric constant includes both ferroelectric with non-ferroelectric fillers. This may improve, not only the dielectric constant of the nanocomposite but also provide additional thermal, electrical, optical, mechanical, or chemical properties to the nanocomposite for specific applications.

Abstract: Methods for preparing a composition containing amorphous iron oxide hydroxide. Methods for regeneration of the amorphous iron oxide hydroxide after it has been used as desulfurizer. Regenerable desulfurizer with high sulfur capacity containing amorphous iron oxide hydroxide, not less than 88% w/w, and organic binder not less than 7% w/w. The organic binder is sodium carboxymethylcellulose, sesbania powder, cellulose powder, or a mixture thereof. A method for preparing the desulfurizer. A method for regenerating the waste agent produced after the desulfurizer and the composition containing the desulfurizer are used as desulfurizer. This method allows the desulfurizer and the composition containing the desulfurizer to be regenerated and reused avoiding the need for landfill disposal and environmental pollution.

Abstract: The smoke suppressant comprises a molybdate precipitate on the surface of a borate core. The precipitate increases surface area of the core and provides improved smoke suppression relative to a mixture of the molybdate and borate core. The suppressants can be incorporated into polymer compositions to improve their smoke suppression capability.

Abstract: Methods for producing electronic grade metal nanostructures having low levels of contaminants are provided. Monolayer arrays, populations, and devices including such electronic grade nanostructures are described. In addition, novel methods and compositions for production of Group 10 metal nanostructures and for production of ruthenium nanostructures are provided, along with methods for recovering nanostructures from suspension.

Abstract: The invention provides inter alia a mineral complex comprising about 40 wt. % to about 60 wt. % SiO2, about 6 wt. % to about 16 wt. % Fe2O3, about 4 wt. % to about 12 wt. %. CaO, about 2 wt. % to about 8 wt. % MgO, wherein at least 85% of the mineral complex has a particle size of about 10 to about 6000 mesh, related compositions and methods for their use, including for growth medium augmentation and remediation.

Abstract: A flat metal particle-containing composition including flat metal particles containing silver and a metal nobler than the silver, wherein the metal nobler than the silver is located near surfaces of the flat metal particles and wherein an amount of the metal nobler than the silver is 10?3 atomic % to 5 atomic % relative to the silver contained in the flat metal particles.

Abstract: A sintered body includes an indium oxide crystal, and an oxide solid-dissolved in the indium oxide crystal, the oxide being oxide of one or more metals selected from the group consisting of aluminum and scandium, the sintered body having an atomic ratio “(total of the one or more metals)/(total of the one or more metals and indium)×100)” of 0.001% or more and less than 45%.