Abstract: As a novel sulfide compound having a low elastic modulus while retaining the high ion conductivity, a sulfide compound for a solid electrolyte of a lithium secondary battery that includes a crystal phase of a cubic argyrodite type crystal structure, and is represented by the compositional formula: Li7?xPS6?xClyBrz, wherein x in the compositional formula satisfies x=y+z and 1.0<x?1.8, and a ratio (z/y) of the molar ratio of Br to the molar ratio of Cl is from 0.1 to 10.0 is proposed.

Abstract: A method of removing one or more target impurities from crude hydrogen bis(fluorosulfonyl)imide (HFSI) using a crystallization technique. In some embodiments, the method includes contacting the crude HFSI with at least one anhydrous solvent to create a solution. The solution is caused to have a temperature sufficient to cause HFSI in the solution to crystalize while the one or more impurities remain dissolved in the mother liquor of the solution. The crystalized HFSI and the mother liquor containing the one or more impurities are separated to obtained a purified HFSI product. Purified HFSI products are also disclosed, as are systems, such as secondary batteries, incorporating purified HFSI products.

Abstract: Provided is a ternary inorganic compound crystal having a molecular formula of Ca8Al12P2O31, and a preparation method thereof comprising the following steps: weighing calcium salts, aluminum salts and phosphate respectively according to the molar ratio of calcium, aluminum and phosphorus in the molecular formula Ca8Al12P2O31; calcining at 1550˜1570° C., cooling, and grinding to obtain the ternary inorganic compound crystal. Also provided is an application of the ternary inorganic compound in gelling materials and molecular sieves, nonlinear optical crystals, and photochromic materials.

Abstract: Proposed is a new sulfide-based solid electrolyte for lithium ion batteries, the sulfide-based solid electrolyte relating to a compound that has a cubic argyrodite type crystal structure and is represented by Li7-x-2yPS6-x-yClx, and having excellent water resistance and oxidation resistance. Proposed is a sulfide-based solid electrolyte for lithium ion batteries, the sulfide-based solid electrolyte containing a compound that has a cubic argyrodite type crystal structure and is represented by compositional formula (1): Li7-x-2yPS6-x-yClx, in which compositional formula, conditions: 0.8?x?1.7 and 0<y??0.25x+0.5 are satisfied.

Abstract: The present disclosure is directed toward a composition and method of treating and preventing infection of pathogenic microorganisms and endopyhtic microorganisms in a plant through the use of phosphite compositions.

Abstract: A solid electrolyte including as constituent components, lithium, phosphorous and sulfur; wherein, in the 31P-NMR, the solid electrolyte has a peak (first peak) in a region of 81.0 ppm or more and 88.0 ppm or less, the solid electrolyte does not have a peak in regions other than the region of 81.0 ppm or more and 88.0 ppm or less, or even if it has a peak in other regions than the region of 81.0 ppm or more and 88.0 ppm or less, the peak intensity thereof relative to the first peak is 0.5 or less, and the solid electrolyte has an ionic conductivity of 5×10?4 S/cm or more.

Abstract: A solid electrolyte including an alkali metal element, phosphorous, sulfur and halogen as constituent components.

Abstract: To provide an imide salt represented by the formula wherein, R represents a halosulfonyl group (—SO2X1 where X1 is a halogen such as fluorine, chlorine, bromine and iodine) or dihalophosphoryl group (—POX2X3 where X2 and X3 are the same or different halogens such as fluorine, chlorine, bromine and iodine), and M represents an alkali metal; with high selectivity and high efficiency by using a low-cost starting material. In the production of an imide salt, an alkali metal fluoride, a sulfuryl halide or phosphoryl halide, and ammonia or an ammonium salt are reacted. According to this method, a desired imide salt can be produced with high yield, while greatly suppressing the production of a by-product.

Abstract: Disclosed is a method for producing “a salt or a complex comprising imide and an organic base”, characterized by reacting halogenated sulfuryl or halogenated phosphoryl with ammonia in the presence of an organic base. According to this method, a target imide compound can be produced in a high yield while significantly suppressing the production of by-products. Further, by reacting the obtained imide compound with an alkali metal hydroxide or an alkaline earth metal hydroxide, an imide metal salt can be easily derived.

Abstract: The present disclosure is directed toward a composition and method of treating and preventing infection of pathogenic microorganisms and endopyhtic microorganisms in a plant through the use of phosphite compositions.

Abstract: There is provided a method for producing an electrolyte solution for lithium ion batteries, in which lithium hexafluorophosphate is used as an electrolyte, comprising the steps of (a) reacting phosphorus trichloride, chlorine and lithium chloride in a nonaqueous organic solvent; and (b) reacting a reaction product of the step (a) formed in the solvent, with hydrogen fluoride.

Abstract: As population density increases, the transportation of hazardous chemicals, including acids and disinfectants, lead to an increased incidence of spills while the consequences of spills become more serious. While solutions of halide acids, hypohalites and halites are safer disinfectants for transportation, handling, storage and use than traditional gaseous chlorine, the manufacturing cost of these disinfectants has here-to-fore limited their use. Economical processes are presented for the manufacture of O2, halogen oxides, halide acids, hypohalites, and halates; as well as polynucleate metal compounds, metal hydroxides and calcium sulfate hydrate (gypsum). The instant invention presents methods and processes that incorporate the use of sulfur. This is while environmental regulators, such as the US EPA, require an increased removal of sulfur from hydrocarbon fuels, thereby creating an abundance of sulfur, such that the refining industry is in need of a way to dispose of said abundance of sulfur.

Abstract: The disclosure provides a process for removing phosphorus-containing colloids and their precursors from an iron chloride solution comprising: (a) heating the iron chloride solution comprising impurities selected from the group consisting of phosphorus-containing colloid, phosphorus-containing colloid precursor, and mixtures thereof, at a temperature of about 100° C. to about 300° C., at least autogenous pressure and for a period of time sufficient to transform the impurities into a filterable solid; and (b) separating the solid from the iron chloride solution. In one embodiment, the iron chloride solution is a byproduct of the chloride process for making titanium dioxide.

Abstract: To provide an imide salt represented by the formula wherein, R represents a halosulfonyl group (—SO2X1 where X1 is a halogen such as fluorine, chlorine, bromine and iodine) or dihalophosphoryl group (—POX2X3 where X2 and X3 are the same or different halogens such as fluorine, chlorine, bromine and iodine), and M represents an alkali metal; with high selectivity and high efficiency by using a low-cost starting material. In the production of an imide salt, an alkali metal fluoride, a sulfuryl halide or phosphoryl halide, and ammonia or an ammonium salt are reacted. According to this method, a desired imide salt can be produced with high yield, while greatly suppressing the production of a by-product.

Abstract: The invention is directed to a process for the manufacture of a ceria based polishing composition, comprising (a) suspending an inorganic cerium salt or cerium hydroxide with a cerium content calculated as cerium oxide in the range of 50%-100% based on Total rare earth oxide (TREO) in an aqueous medium thereby obtaining an aqueous suspension, (b) treating said aqueous suspension with an acid or a salt of an acid selected from the group of HF, H3PO4 and H2SO4, thereby obtaining a solid suspended in said aqueous medium, (c) separating said solid from said aqueous medium, and (d) calcining the separated solid at a temperature between 750° C. and 1,200° C. and grinding the calcined solid to grain sizes in the range of 0.5 ?m to 5.0 ?m.

Abstract: A highly active and environment-friendly catalyst for use in a living radical polymerization is provided. A catalyst for use in a living radical polymerization method is provided. The catalyst comprises a central element, which is selected from nitrogen and phosphorus, and at least one halogen atom, which is bound to the central element. A monomer having a radical reactive unsaturated bond is subjected to a radical polymerization reaction in the presence of the catalyst, thereby it is possible to obtain a polymer having narrow molecular weight distribution. The present invention has the merits such as low toxicity of the catalyst, a small amount of the catalyst being required, high solubility of the catalyst in the polymerization media, mild reaction conditions, no coloration, no odor (unnecessary post-treatment of molded products). The method of the present invention is more environment-friendly and economical than other living radical polymerization methods.

Abstract: The invention relates to lithium argyrodite of the general formula (I): Li+(12-n-x)Bn+X2?6-xY?x(I), where Bn+ is selected from the group P, As, Ge, Ga, Sb, Si, Sn, Al, In, Ti, V, Nb, and Ta, X2? is selected from the group S, Se, and Te, Y? is selected from the group Cl, Br, I, F, CN, OCN, SCN, N3, and where 0?x?2, and a method for the production thereof, and the use thereof as a lithium-ion electrolyte in primary and secondary electrochemical energy storage.

Abstract: A composite oxide catalyst for the oxidation of an olefin containing Mo and Bi as essential components, characterized in that it has a specific surface area of 5 to 25 m2/g and a pore volume of 0.2 to 0.7 cc/g, and has a pore diameter distribution wherein the volume of the pores having a pore diameter of 0.03 to 0.1 ?m accounts for 30% or more of the total pore volume, the volume of the pores having a pore diameter of 0.1 to 1 ?m accounts for 20% or more of the total pore volume, and the volume of the pores having a pore diameter of less than 0.

Abstract: The present invention provides a method for producing cyclic chlorophosphazene oligomers, in particular the trimer and tetramer, in a high yield and selectivity. The method for producing cyclic chlorophosphazene oligomers involves the reaction between chlorinated phosphorus and ammonium chloride in the presence of a reaction catalyst, wherein 1) moisture is present in the reaction system at a molar fraction of 5×10?3 or less based on the total moles of the chlorinated phosphorus added to the reaction system, and 2) the ammonium chloride has an average particle size of 10 ?m or less and the value of particle size distribution of 2 or more, estimated by the Rosin-Rammler equation.

Abstract: The present invention provides a method for producing cyclic chlorophosphazene oligomers, in particular the trimer and tetramer, in a high yield and selectivity. The method for producing cyclic chlorophosphazene oligomers involves the reaction between chlorinated phosphorus and ammonium chloride in the presence of a reaction catalyst, wherein 1) moisture is present in the reaction system at a molar fraction of 5×10−3 or less based on the total moles of the chlorinated phosphorus added to the reaction system, and 2) the ammonium chloride has an average particle size of 10 &mgr;m or less and the value of particle size distribution of 2 or more, estimated by the Rosin-Rammler equation.

Abstract: A process of preparing an inorganic compound is disclosed, comprising the steps of (a) allowing at least an inorganic raw material compounds (A) and an inorganic raw material compound (B) which are different in solubility in water to react with each other in the presence of a reaction solvent with stirring to deposit an inorganic compound (C), while allowing a part of each of the compound (A) and compound (B) to exist as a solid; and

Abstract: Disclosed is a process for producing phosphorous trichloride, phosphorous pentachloride, or phosphorous tribromide by reacting phosphine gas with chlorine gas or bromine gas, in a mixture with hydrogen gas. The phosphine is dried and the reaction is performed at a temperature up to about 250° C. The phosphorous trichloride or phosphorous tribromide product can be reacted with oxygen to form phosphorous oxychloride or phosphorous oxybromide, respectively.

Abstract: from Groups 2, 3, 12, 13, or 14 of the Periodic Table. Preferred embodiments include those having where c=1, those where c=2, and those where c=3. Preferred embodiments include those where a ≦1 and c=1, those where a=2 and c=1, and those where a≧3 and c=3. This invention also provides electrodes comprising an electrode active material of this invention, and batteries that comprise a first electrode having an electrode active material of this invention; a second electrode having a compatible active material; and an electrolyte.

Abstract: The invention provides new and novel lithium-metal-fluorophosphates which, upon electrochemical interaction, release lithium ions, and are capable of reversibly cycling lithium ions. The invention provides a rechargeable lithium battery which comprises an electrode formed from the novel lithium-metal-fluorophosphates. The lithium-metal-fluorophosphates comprise lithium and at least one other metal besides lithium.

Abstract: Most part of an amount of uranium contained in the spent nuclear fuel is removed by making fluorine or a fluorochemical act on the spent nuclear fuel to convert the uranium into UF6, and the uranium is purified through a simple method of distilling the UF6 together with a absorbent. After removing the most part of the amount of uranium, the remaining nuclear fuel material is dissolved and then transferred to an extraction process to recover plutonium. By doing so, a small sized dry process can be employed as a uranium purification process. Since the nuclear fuel material is dissolved and extracted after removing most part of an amount of uranium, a volume of processing solution can be reduced and the machine installation scale can be made small. Accordingly, the reprocessing facility can be extremely downsized.

Abstract: A process for removing impurities contained in the crystal lattice of minerals, comprising the steps of forming a mixture of a mineral capable of structurally reorganizing its crystal lattice which contains an impurity in its crystal lattice and a halogen anion, and water; heating the mixture to the mineral's structural reorganization transition temperature; holding the mixture at the structural reorganization transition temperature for a sufficient period of time to allow the impurity to freely migrate from the lattice to combine with the halogen anion; and separating the combined impurity and anion from the mixture to render the mineral essentially free of the impurity. The process is applicable to numerous minerals and impurities, but is especially useful to remove arsenic from fluorspar. Numerous halogen anions can be employed, such as chlorides, fluorides, bromides and iodides, but the preferred halogen anion is a metal chloride such as calcium chloride.

Abstract: Processes are provided for preparation of precursors of Group III-V compounds, i.e., nitrides, phosphides, arsenides, antimonides and bismuthides of boron, aluminum, gallium and indium. The precursors are easily converted, e.g., by thermal decomposition, to the Group III-V compounds which are useful as thin-film coatings for aerospace components or as powders which may be shaped as desired.

Abstract: Phosphonitrile halides are prepared employing the use of disilazanes. The resultant products may be further reacted with cyclosiloxanes to form siloxane containing phosphonitrile halides.

Abstract: A method for making poly(dichlorophosphazene) using solid state reactants is disclosed and described. The present invention improves upon previous methods by removing the need for chlorinated hydrocarbon solvents, eliminating complicated equipment and simplifying the overall process by providing a “single pot” two step reaction sequence. This may be accomplished by the condensation reaction of raw materials in the melt phase of the reactants and in the absence of an environmentally damaging solvent.

Abstract: A coagulant which is the reaction product of a trivalent metal salt (eg., FeCl3), excluding chromium salts, an acid phosphorous compound and an aluminum hydroxy chloride, and a process for preparing such coagulant. This coagulant may be effectively used to remove suspended solids and various impurities in most water treatment applications.

Abstract: The present invention relates to an improved process for the preparation of thiophosphoryl chloride which is useful as an intermediate for the synthesis of insecticidally active compounds. The improvement comprises the presence in the reaction mixture of a catalytic amount of a nitroxide free radical of the following general formula: wherein R1, R2, R3 and R4 represent an alkyl group.

Abstract: A process for the preparation of &agr;-chloromethylene-triorganylphosphorane derivatives I (radicals R are C-organic substituents and A stands for CN or CO-B where B is a C-organic or O-organic radical which is inert under chlorination conditions) by chlorination of phosphoranes II with chlorine, wherein the chlorination is carried out in the presence of a mineral base as hydrogen chloride acceptor and the chlorine and base are fed to the reaction mixture concurrently but separately at the rates at which they are consumed. The reaction products I are important intermediates for plant protectants.

Abstract: A process for removing impurities contained in the crystal lattice of minerals, comprising the steps of forming a mixture of a mineral capable of structurally reorganizing its crystal lattice which contains an impurity in its crystal lattice and a halogen anion, and water; heating the mixture to the mineral's structural reorganization transition temperature; holding the mixture at the structural reorganization transition temperature for a sufficient period of time to allow the impurity to freely migrate from the lattice to combine with the halogen anion; and separating the combined impurity and anion from the mixture to render the mineral essentially free of the impurity. The process is applicable to numerous minerals and impurities, but is especially useful to remove arsenic from fluorspar. Numerous halogen anions can be employed, such as chlorides, fluorides, bromides and iodides, but the preferred halogen anion is a metal chloride such as calcium chloride.

Abstract: An nickel hydroxide positive electrode active material which can be made by an ultrasonic precipitation method. The nickel hydroxide active material is characterized by the composition: ##EQU1## where x, the number of water ligands surrounding each Ni cation, is between 0.05 and 0.4 and y is the charge on the anions.

Abstract: A process for the purification of recovered or regenerated phosphorus oxychloride contaminated by reactive organic compounds, by reacting the contaminated phosphorus oxychloride with from 0.1 to 5% by weight of an organic amine, having 1 or 2 tertiary N-atoms and a boiling point above the boiling point of phosphorus oxychloride, at the boiling temperature of the reaction mixture and subsequently carrying out fractional distillation at atmospheric pressure to obtain purified phosphorus oxychloride.

Abstract: Carbonated hydroxyapatite compositions and their preparation are described. The compositions are biologically resorbable and are prepared as flowable masses which can be administered by syringe to set in situ to serve as a support structure, filler, prosthesis or the like. Optionally the compositions may include proteins or serve as a depot for compositions of phrarmacological interest.

Abstract: Carbonated hydroxyapatite compositions and their preparation are described. The compositions are biologically resorbable and are prepared as flowable masses which can be administered by syringe to set in situ to serve as a support structure, filler, prosthesis or the like.

Abstract: Impure POCl.sub.3 is purified by distillation in the presence of high-boiling nitrogen compounds from the group consisting of the substituted pyridines and pyrimidines, the open-chain and cyclic aliphatic amines, the open-chain and cyclic amidines, the guanidines and the aromatic amines.

Abstract: A method for producing a polyorganophosphazene, such as, for example, poly?di(carboxylatophenoxy)phosphazenel!, from polydichlorophosphazene. The polydichlorophosphazene is reacted with at least one nucleophilic reagent at a defined molar ratio of the at least one nucleophilic reagent to the polydichlorophosphazene. Such process results in the production of a polyorganophosphazene having a molecular weight within a desired range.

Abstract: This invention relates generally to inorganic ionic liquids which function as electrolytes and do not crystallize at ambient temperature. More specifically, this invention is directed to quasi-salt inorganic ionic liquids which comprise the reaction product of a strong Lewis acid with an inorganic halide-donating molecule. This invention is further directed to quasi-salt inorganic ionic liquid mixtures which comprise combinations of electrolyte additives and quasi-salt inorganic ionic liquids. These quasi-salt inorganic ionic liquid mixtures are useful electrolytes.

Abstract: This invention relates generally to electrolyte solvents for use in liquid or rubbery polymer electrolyte solutions as are used, for example, in electrochemical devices. More specifically, this invention relates to sulfonyl/phospho-compound electrolyte solvents and sulfonyl/phospho-compound electrolyte solutions incorporating such solvents.

Abstract: The reaction of phosphorus pentachloride with ammonium chloride is conducted in the presence of a metal-containing catalyst and carbon dioxide, preferably supercritical carbon dioxide, as a solvent. The product is generally superior in catalytic action for the polycondensation and rearrangement of organosiloxanes to conventional linear phosphonitrilic chlorides.

Abstract: A solution which comprises a polyphosphazene solute, such as a polyhalophosphazene solute, and a stabilizing solvent such as diglyme. Such solution enables the polyphosphazene to remain stable for extended periods of time so that such polyhalophosphazenes may be employed for further modification or use.

Abstract: A process to manufacture high purity thionyl chloride and phosphorus oxychloride utilizing a fluctuating flow of sulfur dioxide. Chlorine, sulfur dioxide, and phosphorus trichloride are reacted in a process that limits the amount of sulfuryl chloride and/or phosphorus trichloride remaining in the product stream. Cl.sub.2 and SO.sub.2 are first reacted to form SO.sub.2 Cl.sub.2, which, in turn, is reacted with excess PCl.sub.1 to form the products, POCl.sub.3 and SOCl.sub.2. Any excess PCl.sub.3 is then reacted with additional Cl.sub.2 and SO.sub.2 to form additional product. Alternatively, Cl.sub.2, SO.sub.2, and PCl.sub.13 are reacted directly to form POCl.sub.3 and SOCl.sub.2 without the formation of any SO.sub.2 Cl.sub.2 intermediate by utilizing a continuous stirred loop reactor.

Abstract: Disclosed herein is an improved process for preparing a thiophosphoryl chloride comprising reacting sulfur with a phosphorous trichloride, the improvement comprising a catalytic amount of a tertiary amine catalyst.

Abstract: Unreacted phosphorus and heavy metals, such as arsenic and antimony, are removed in environmentally acceptable form from the non-aqueous still bottoms residue resulting from the production of PCl.sub.3, by reacting the residue with an excess of calcium hydroxide in the form of an aqueous lime slurry and separating the reaction product into a precipitate and a filtrate. The reaction with lime slurry may be preceded by hydrolysis with water. The precipitate passes the Toxicity Characteristic Leaching Procedure (TCLP) test and the filtrate contains less than 5 ppm of the heavy metals, thus permitting disposal by landfill and sewering, respectively, under EPA regulations.

Abstract: Short-chain linear phosphazenes as well as products of their reactions with water, alcohols and organosiloxanes, and the like, are active catalysts for polycondensation and redistribution of organosiloxane polymers.

Abstract: .sup.32 P-Thiophosphates of the general formula: ##STR1## wherein n =1, 2 or 3 and each M, which may be the same or different, is H or a cation, are prepared by heating H.sub.3.sup.32 PO.sub.4 or a salt thereof with at least an equivalent amount of a thiophosphoryl halide and then treating the reaction product with an aqueous medium to hydrolyse the reaction product and form the .sup.32 P thiophosphate.

Abstract: There is disclosed an improved process for the preparation of phosphorus trichloride wherein elemental phosphorus is caused to react with chlorine. The improvement comprises continuous, high speed analysis of the contents of the reactor whereby the reaction is controlled to produce less phosphorus pentachloride and other by-products. The analysis is performed by a laser Raman spectrometer associated with an optrode having a remotely located probe head and a circulating sampling system to continuously provide fresh sample to the probe head continuously. Also disclosed is apparatus for the automatic control of the reaction by control of the reactant feed to the reactor in response to the on-line, continuous analysis of the reactor contents.

Abstract: There is disclosed an improved process for the semi-continuous production of phosphorus trichloride by the reaction of elemental phosphorus and chlorine in a liquid phosphorus trichloride layer. In accordance with the present invention periodic termination of the process by discontinuing phosphorus feed thereby creating a heel containing residual phosphorus is rendered more safe and less waste is produced by the improvement which comprises chlorinating the residual phosphorus at a substantially constant flow rate and continuing the chlorine feed rate until after observing at least one of either a step-wise decrease in the pressure within the reactor or a step-wise decrease in the flow rate of phosphorus trichloride removed from the reactor and then terminating the chlorine feed when said pressure and flow rate achieve a substantially steady state at a lower value.