Abstract: A hydrogen-trapping compound is provided, along with a process for manufacturing the compound, and its uses, wherein the hydrogen-trapping compound is characterized in that it contains at least one metal salt of formula MX(OH), in which M represents a divalent transition element, for example Co or Ni; O represents an oxygen atom; X represents an atom of group 16 of the Periodic Table of the Elements, excluding O, for example a sulphur atom; and H represents a hydrogen atom, and wherein the hydrogen-trapping compound is effective for trapping hydrogen, hydrogen within a material and free hydrogen and is applicable in situations in which hydrogen is evolved and in which it has to be trapped, especially for safety reasons.

Abstract: Sulphidation method for a UO2 powder, in which said powder is sulfurated by bringing it into contact with a gaseous sulphidation agent. Method for manufacturing nuclear fuel pellets based on uranium oxide, or mixed oxide of uranium and plutonium, from a load of totally or partially sulfurated UO2 powder or UO2 powder and PuO2 powder, by lubrication, pelletizing and sintering, in which: the load of powder subjected to the lubrication, pelletizing and sintering is prepared by the following successive steps: sulphidation of a UO2 powder by the above sulphidation method; optionally mixing, said sulfurated powder in a matrix comprising a UO2 powder, or of a UO2 powder and a PuO2 powder; and, subjecting said load, formed from said sulfurated powder or said mixture, to lubrication, pelletizing and sintering operations.

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 discloses a process for producing nano-powders and powders of nano-particle loose aggregate, which includes: (a) providing at least two reactant solutions A and B capable of rapidly reacting to form deposits; (b) supplying the at least two reactant solutions A and B at least at the reaction temperature into a mixing and reaction precipitator respectively, in which mixing reaction and precipitation are continuously carried out in sequence, the mixing and reaction precipitator being selected from at least one of a tubular ejection mixing reactor, a tubular static mixing reactor and an atomization mixing reactor; and (c) treating the deposit-containing slurry continuously discharged from the mixing reaction precipitator.

Abstract: A method of preparing metal chalcogenide particles. The method comprising the step of reacting an amine and metal complex precursors. The metal complex precursors comprising a chalcogenide and an electrophilic group. The reaction forming metal chalcogenide particles substantially free of the electrophilic group.

Abstract: A method and structure for making magnetite nanoparticle materials by mixing iron salt with alcohol, carboxylic acid and amine in an organic solvent and heating the mixture to 200–360 C is described. The size of the particles can be controlled either by changing the iron salt to acid/amine ratio or by coating small nanoparticles with more iron oxide. Magnetite nanoparticles in the size ranging from 2 nm to 20 nm with a narrow size distribution are obtained with the invention. The invention can be readily extended to other iron oxide based nanoparticle materials, including MFe2O4 (M=Co, Ni, Cu, Zn, Cr, Ti, Ba, Mg) nanomaterials, and iron oxide coated nanoparticle materials. The invention also leads to the synthesis of iron sulfide based nanoparticle materials by replacing alcohol with thiol in the reaction mixture.

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 process for preparation of an ammonium polythiomolybdate or a hydrate thereof of the formula (NH4)2Mo3S13.n H2O where n is 0, 1 or 2, in which aqueous ammonium monosulfide, elemental sulfur and molybdic oxide are reacted in a sealed reactor, with hydrogen sulfide gas being fed into the reactor until the hydrogen sulfide is no longer absorbed by the reaction mixture to form a reaction product and then heating the reaction product in a sealed reactor, the concentration of ammonium monosulfide in the reaction mixture being controlled throughout the reaction such that reactor pressure does not exceed 700 kPa (100 psig).

Abstract: Active materials of the invention contain at least one alkali metal and at least one other metal capable of being oxidized to a higher oxidation state. Preferred other metals are accordingly selected from the group consisting of transition metals (defined as Groups 4–11 of the periodic table), as well as certain other non-transition metals such as tin, bismuth, and lead. The active materials may be synthesized in single step reactions or in multi-step reactions. In at least one of the steps of the synthesis reaction, reducing carbon is used as a starting material. In one aspect, the reducing carbon is provided by elemental carbon, preferably in particulate form such as graphites, amorphous carbon, carbon blacks and the like. In another aspect, reducing carbon may also be provided by an organic precursor material, or by a mixture of elemental carbon and organic precursor material.

Abstract: A process for the production of a lithium transition metal sulphide such as lithium iron sulphide, the process comprising reacting a transition metal sulphide with lithium sulphide in a solvent comprising a molten salt or a mixture of molten salts. Lithium transition metal sulphides obtained using this process are useful in the production of electrodes, in particular for rechargeable lithium batteries.

Abstract: A process for producing an ammonium polythiomolybdate of the formula (NH4)2Mo3S13.n H2O where n is 0, 1 or 2 in which an aqueous ammoniacal molybdate solution is reacted with hydrogen sulfide gas in a closed system at superatmospheric pressure until the H2S is no longer absorbed by the solution to form a slurry of solid ammonium tetrathiomolybdate containing a portion of the starting molybdenum in a mother liquor containing the balance of the molybdenum and thereafter heat soaking the reaction product in the presence of elemental sulfur to form the desired product.

Abstract: Novel iron sulfides having excellent durability and excellent treating properties of heavy metals, processes for producing the iron sulfides, iron sulfide mixture, a heavy metal treating agent containing either of these novel iron sulfides as an effective component, and a method by which wastes containing various heavy metals are treated with the heavy metal treating agent are disclosed. The iron sulfide having a mackinawite structure which contains FeMxNySz wherein M represents an alkaline earth metal, N represents an alkali metal, and x, y and z, indicating the molar proportions of the respective elements, represent numbers satisfying 0.01<x?0.5, y?0.2 and 0.7?z?1.4, as an essential component.

Abstract: A method of continuously producing a non-oxide ceramic formed of a metal constituent and a non-metal constituent. A salt of the metal constituent and a compound of the non-metal constituent and a compound of the non-metal constituent are introduced into a liquid alkali metal or a liquid alkaline earth metal or mixtures to react the constituents substantially submerged in the liquid metal to form ceramic particles. The liquid metal is present in excess of the stoichiometric amount necessary to convert the constituents into ceramic particles to absorb the heat of reaction to maintain the temperature of the ceramic particles below the sintering temperature. Ceramic particles made by the method are part of the invention.

Abstract: Compounds are expressed by general formula of AxBC2−y where 0≦x≦2 and 0≦y<1, and have CdI2 analogous layer structures; A-site is occupied by at least one element selected from the group consisting of Li, Na, K, Rb, Cs, Mg, Ca, Sr, Ba, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, Zr, Nb, Mo, Ru, Rh, Pd, Ag, Cd, Hf, Ta, W, Re, Ir, Pt, Au, Sc, rare earth elements containing Y, B, Al, Ga, In, Tl, Sn, Pb and Bi; B-site is occupied by at least one element selected from the group consisting of Ti, V, Cr, Zr, Nb, Mo, Hf, Ta, W, Ir, and Sn; C-site is occupied by at least one element selected from the group consisting of S, Se and Te; the compounds exhibit large figure of merit so as to be preferable for thermoelectric generator/refrigerator.

Abstract: A structure directing agent is removed from a microporous solid at a temperature below the temperature that would cause the structure directing agent to decompose by cleaving the structure directing agent within the pores of the microporous solid, at a temperature below the temperature that would cause the structure directing agent to decompose, into two or more fragments and removing the fragments from the pores of the microporous solid at a temperature below the temperature that would cause the structure directing agent or its fragments to decompose.

Abstract: A nonaqueous electrolyte battery includes a positive electrode containing a positive electrode active material, a negative electrode containing a sulfide containing Fe, and a nonaqueous electrolyte including a nonaqueous solvent and a solute dissolved in the nonaqueous solvent, the nonaqueous solvent containing a first solvent containing a cyclic carbonate and a second solvent containing a chain carbonate, wherein the content of the first solvent in the nonaqueous solvent falls within a range of between 4.8 and 29% by volume and the content of the second solvent in the nonaqueous solvent falls within a range of between 71 and 95.2% by volume.

Abstract: A process for the production of a lithium transition metal sulphide such as lithium iron sulphide, the process comprising reacting a transition metal sulphide with lithium sulphide in a solvent comprising molten sulphur. Lithium transition metal sulphides obtained using this process are also claimed and are useful in the production of electrodes, in particular for rechargeable lithium batteries.

Abstract: A process for the production of a lithium transition metal sulphide such as lithium iron sulphide, the process comprising reacting a transition metal sulphide with lithium sulphide in a solvent comprising a molten salt or a mixture of molten salts. Lithium transition metal sulphides obtained using this process are also claimed and are useful in the production of electrodes, in particular for rechargeable lithium batteries.

Abstract: Novel iron sulfides having excellent durability and excellent treating properties of heavy metals, processes for producing the iron sulfides, iron sulfide mixture, a heavy metal treating agent containing either of these novel iron sulfides as an effective component, and a method by which wastes containing various heavy metals are treated with the heavy metal treating agent are disclosed. The iron sulfide having a mackinawite structure which contains FeMxNySz wherein M represents an alkaline earth metal, N represents an alkali metal, and x, y and z, indicating the molar proportions of the respective elements, represent numbers satisfying 0.01<x≦0.5, y≦0.2 and 0.7≦z≦1.4, as an essential component.

Abstract: A process for the production of a vanadium compound from carbonaceous residues containing vanadium, which includes the steps of: (a) combusting the carbonaceous residues at a temperature of 500-690° C. in an oxygen-containing gas to form vanadium-containing combustion residues; (b) heating the vanadium-containing combustion residues at a temperature T in ° C. under an oxygen partial pressure of at most T in kPa wherein T and P meet with the following conditions: log10(P)=−3.45×10−3×T+2.21 500≦T≦1300 to obtain a solid product containing less than 5% by weight of carbon and vanadium at least 80% of which is tetravalent vanadium oxide; (c) selectively leach tetravalent vanadium ion with sulfuring acid at pH in the range of 1.5-4; (d) separating a liquid phase from the leached mixture; (e) adding an alkaline substance to the liquid phase to adjust the pH thereof in the range of 4.5-7.

Abstract: A fuel processing system is operative to remove substantially all of the sulfur present in a logistic fuel stock supply. The fuel stock can be gasoline, diesel fuel, or other like fuels which contain relatively high levels of organic sulfur compounds such as mercaptans, sulfides, disulfides, and the like. The system is a part of a fuel cell power plant. The fuel stock supply is fed through a reformer where the fuel is converted to a hydrogen rich fuel which contains hydrogen sulfide. The hydrogen sulfide-containg reformer exhaust is passed through a sulfur scrubber, to which is added a small quantity of air, which scrubber removes substantially all of the sulfur in the exhaust stream by means of the Claus reaction. The desulfurizing step causes sulfur to deposit on the scrubber bed, which after a period of time, will prevent further sulfur from being removed from the reformer exhaust stream.

Abstract: Disclosed is a method of preparing a positive active material for a rechargeable lithium battery. In this method, a lithium salt is reflux-reacted with a metal salt in a basic solution. The positive active material has a spherical or sperical-like form, diameter of 10 nm to 10 &mgr;m, and a surface area of 0.1 to 5 m2/g.

Abstract: A procedure for the production of polymeric sulfur with improved stability that comprises the stages of: (a) cooling in a vessel for rapid cooling the sulfur vapor from the vaporization of molten sulfur, by bringing it into direct contact with a refrigerating suspension composed of carbon disulphide, soluble sulfur and polymeric sulfur, to a temperature such that part of the sulfur vapor is transformed into a powder-like polymeric sulfur, insoluble in carbon disulphide. (b) extracting the resulting suspension from the cooling vessel; (c) recycling part of said suspension to the vessel for cooling; and (d) sending the rest of the suspension to a maturation stage to stabilize the polymeric sulfur.

Abstract: Compounds are expressed by general formula of AxBC2−y where 0≦x≦2 and 0≦y<1, and have CdI2 analogous layer structures; A-site is occupied by at least one element selected from the group consisting of Li, Na, K, Rb, Cs, Mg, Ca, Sr, Ba, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, Zr, Nb, Mo, Ru, Rh, Pd, Ag, Cd, Hf, Ta, W, Re, Ir, Pt, Au, Sc, rare earth elements containing Y, B, Al, Ga, In, Tl, Sn, Pb and Bi; B-site is occupied by at least one element selected from the group consisting of Ti, V, Cr, Zr, Nb, Mo, Hf, Ta, W, Ir, and Sn; C-site is occupied by at least one element selected from the group consisting of S, Se and Te; the compounds exhibit large figure of merit so as to be preferable for thermoelectric generator/refrigerator.

Abstract: Novel iron sulfides having excellent durability and excellent treating properties of heavy metals, processes for producing the iron sulfides, iron sulfide mixture, a heavy metal treating agent containing either of these novel iron sulfides as an effective component, and a method by which wastes containing various heavy metals are treated with the heavy metal treating agent are disclosed. The iron sulfide having a mackinawite structure which contains FeMxNySz wherein M represents an alkaline earth metal, N represents an alkali metal, and x, y and z, indicating the molar proportions of the respective elements, represent numbers satisfying 0.01<x≦0.5, y≦0.2 and 0.7≦z≦1.4, as an essential component.

Abstract: The present invention provides a clathrate compound which can be used as a thermoelectric material, a hard material, or a semiconductor material. Silicon or carbon are formed into a clathrate lattice, and a clathrate compound is then formed in which specified doping atoms are encapsulated within the clathrate lattice, and a portion of the atoms of the clathrate lattice are substituted with specified substitution atoms. The clathrate lattice is, for example, a silicon clathrate 34 (Si34) mixed lattice of a Si20 cluster including a dodecahedron of Si atoms, and a Si28 cluster including a hexahedron of Si atoms. Suitable doping atoms are atoms from group 1A, group 2A, group 3A, group 1B, group 2B, group 3B, group 4A, group 5A, group 6A, and group 8, and suitable substitution atoms are atoms from group 1A, group 2A, group 3A, group 1B, group 2B, group 3B, group 5A, group 6A, group 7A, group 5B, group 6B, group 7B, and group 8 of the periodic table.

Abstract: The present invention is a new and simple method of decomposing ammonium tetrathiomolybdate (ATTM) in an organic solvent with added water under H2 pressure. Model compound reactions of 4-(1-naphthylmethyl)bibenzyl (NMBB) were carried out at 350-425° C. under H2 pressure in order to examine the activity of the Mo sulfide catalysts generated from ATTM with and without added water for C—C bond cleavage and hydrogenation of aromatic ring. The Mo sulfide catalysts generated from ATTM with added water were much more effective for C—C bond cleavage and hydrogenation of aromatic moieties at 350-425° C. than those from ATTM alone. Two-step tests revealed that the addition of water is effective for generating highly active Mo sulfide catalyst from ATTM, but water itself does not promote catalytic conversion. Removal of water after the decomposition of ATTM with added water at 350-400° C. under H2 pressure by hot purging gives highly active Mo sulfide catalyst.

Abstract: The present invention relates to a process of oxidation, of the wet oxidation or ozonization type, of a liquid contained in a reactor. The gas of the gas headspace is aspirated into the liquid, and the portion which is not dissolved in the liquid is recovered in the gas headspace. The agitation means creates a flow of liquid immediately adjacent to the end of the duct opening into the liquid, and generates a gas/liquid dispersion in the zone, within which the liquid reacts with the gas, then conveys and ejects the said dispersion at its periphery, such that the gas is dissolved in the liquid in the zone extending from the agitation means to the surface of the liquid. The said process is particularly suitable for oxidations which make use of considerable quantities of oxygen or of ozone. It is particularly applied for the oxidation of papermaking liquors.

Abstract: Sulphides and selenides are prepared by dissolving sulphur or selenium in an aqueous or non-aqueous solution of hydrazine hydrate. The solution is combined with a solution of an appropriate cation to precipitate the corresponding sulphide or selenide. Solutions of two or more cations may be used to produce ternary compounds of sulphur and selenium, for example thio-gallates. Likewise both sulphur and selenium can be used together to produce sulpho-selenides. The method is particularly applicable to the production of doped phosphors by the inclusion of solutions containing the appropriate dopant.

Abstract: The present invention relates to a compound based on an alkaline-earth metal, on sulphur and on aluminium, on gallium or indium, to its process of preparation and to its use as luminophore. The compound of the invention corresponds to the formula AB2S4, in which A represents an alkaline-earth metal and B aluminum, gallium, or indium and it is characterized in that it is provided in the form of a powder with a residual oxygen content of not more that 1.5% and composed of particles with a mean size of not more than 10 &mgr;m. This compound is obtained by a process which contains the following stages: a solution or a suspension comprising salts of the elements A and B is formed, the solution or the suspension is dried by atomization and the product obtained in the preceding stages is reacted with carbon disulphide or with a mixture of hydrogen sulphide and or carbon disulphide. The compound of the invention can be used as a luminophore, in particular in cathodoluminescence.

Abstract: The present invention concerns a sulfide of a rare earth and an alkali, a process for its preparation and its use as a colored pigment. The sulfide is characterized in that it has the formula ABS2 where A represents at least one alkali and B represents at least one rare earth and in that it is constituted by grains with an average size of 1.5 &mgr;m at most. The preparation process for the sulfide is characterized in that at least one rare earth carbonate or hydroxycarbonate is brought into the presence of at least one gas selected from hydrogen sulfide or carbon disulfide. The product obtained is optionally deagglomerated. The sulfide can be used as a pigment in plastics, paints, finishes, rubbers, ceramics, glazes, paper, inks, cosmetics, dyes, laminated coatings and materials based on or obtained from at least one inorganic binder.

Abstract: Electroluminescent phosphor powders and a method for making phosphor powders. The phosphor powders have a small particle size, narrow particle size distribution and are substantially spherical. The method of the invention advantageously permits the economic production of such powders. The invention also relates to improved devices, such as electroluminescent display devices, incorporating the phosphor powders.

Abstract: The present invention is a new and simple method of decomposing ammonium tetrathiomolybdate (ATTM) in an organic solvent with added water under H.sub.2 pressure. Model compound reactions of 4-(1-naphthylmethyl)bibenzyl (NMBB) were carried out at 350-425.degree. C. under H.sub.2 pressure in order to examine the activity of the Mo sulfide catalysts generated from ATTM with and without added water for C--C bond cleavage and hydrogenation of aromatic ring. The Mo sulfide catalysts generated from ATTM with added water were much more effective for C--C bond cleavage and hydrogenation of aromatic moieties at 350-425.degree. C. than those from ATTM alone. Two-step tests revealed that the addition of water is effective for generating highly active Mo sulfide catalyst from ATTM, but water itself does not promote catalytic conversion. Removal of water after the decomposition of ATTM with added water at 350-400.degree. C. under H.sub.2 pressure by hot purging gives highly active Mo sulfide catalyst.

Abstract: The specification discloses an apparatus and method for treating a slurry containing sodium sesquisulfate to recover sulfate and acid constituents therefrom. The apparatus includes a treatment vessel having a separation wall delineating a clarifying zone and a mixing zone. Slurry containing sesquisulfate crystals is introduced into the mixing zone along with water and the material is mixed to promote dissolution of the crystals and formation of sodium sulfate solids. Sodium sulfate solids are collected in a lower portion of the treatment vessel and conveyed out of the vessel, and liquid from the clarifying zone is conducted from an upper end of the treatment vessel to a conventional liquid processing unit. Treatment of a sesquisulfate-containing slurry in accordance with the invention provides sodium sulfate containing little or no sesquisulfate crystals thereby reducing the need for vacuum filtration or other expensive separation techniques to recover sulfuric acid and sodium sulfate solids from the slurry.

Abstract: The present invention is directed towards a system that makes high quality gypsum from a dry flue gas desulfurization process which utilizes a low temperature regeneration of the carbon adsorbent in the flue gas process. The high quality gypsum is easily filterable with large crystal size and has high purity with few contaminants, such as calcium sulfite and heavy metals. This invention is also directed towards a system that regenerates the carbon used in dry flue gas desulfurization at a temperature below 120.degree. C. and the recycling of sodium hydroxide to form a sodium sulfite reducing solution for carbon adsorbent regeneration.

Abstract: The invention relates to a catalyst for the treatment of gases containing sulphur compounds, using the Claus reaction or using hydrolysis, which is made up of alumina-based porous particles and characterized in that the cumulative volume created by all the pores whose diameter is greater than 0.1 .mu.m, V.sub.0.1, is greater than 12 ml/100 g of catalyst and in that the cumulative volume created by all the pores whose diameter is greater than 1 .mu.m, V.sub.1, is such that the ratio V.sub.1 /V.sub.0.1 is higher than or equal to 0.65. This catalyst can be employed for the treatment of gases containing sulphur compounds by using the Claus reaction, or of gases containing organic sulphur compounds by using a hydrolysis reaction.

Abstract: A series of alkali metal bismuth or bismuth and antimony, antimony chalcogenides (Te or S) are described. The compounds have a unique combination electrical properties.

Abstract: A solid lubricant, in particular for friction linings, on the basis of metal sulphides, which contains or consists of at least one compound of the formulaM1M2.sub.m M3.sub.n S.sub.xwherein M1, M2, and M3 each represent one metal of the series of Ti, V, Mn, Fe, Cu, Zn, Mo, W, Sb, Sn and Bi, S denotes sulphur, and the subscripts comprise the ranges of I=1-5, m=1-5, n=0-5 and x=2-8, as well as friction lining mixtures and friction linings containing the same.

Abstract: A stabilized aqueous alkali or alkaline earth metal hypobromite solution is prepared by mixing an aqueous solution of alkali or alkaline earth metal hypochlorite having from about 5 percent to about 70 percent available halogen as chlorine with a water soluble bromide ion source; allowing the bromide ion source and the alkali or alkaline earth metal hypochlorite to react to form a 0.5 to 70 percent by weight aqueous solution of unstabilized alkali or alkaline earth metal hypobromite; adding to the unstabilized solution of alkali or alkaline earth metal hypobromite a suitable stabilizer such as a carbonic acid, hydrogen cyanide, carboxylic acid, amino acid, sulfuric acid, phosphoric acid or boric acid; and recovering a stabilized aqueous alkali or alkaline earth metal hypobromite solution.

Abstract: Method of preparing metal disulfides of the general formula(Sn.sub.x Me.sub.1-x)S.sub.2,whereinMe represents one or more of the elements Ti, Mo, Fe, Cr, Ta, Nb, Mn, Bi, W and Cu, andx can have values between 0.5 and 1,by mixing Sn, alone or with Me and/or Me sulfides, with a superstoichiometric quantity of S and reacting the same together, in the presence of halide compounds, in an exothermic reaction in an inert atmosphereand the further processing the disulfide product thereof to form dimetal trisulfides.

Abstract: The invention is a method for preparing a stabilized aqueous alkali or alkaline earth metal hypobromite solution. The method comprises the steps of:a. Mixing an aqueous solution of alkali or alkaline earth metal hypochlorite having from about 5 percent to about 70 percent available halogen as chlorine with a water soluble bromide ion source;b. Allowing the bromide ion source and the alkali or alkaline earth metal hypochlorite to react to form a 0.5 to 70 percent by weight aqueous solution of unstabilized alkali or alkaline earth metal hypobromite;c. Adding to the unstabilized solution of alkali or alkaline earth metal hypobromite an aqueous solution of an alkali metal sulfamate in a quantity to provide a molar ratio of alkali metal sulfamate to alkali or alkaline earth metal hypobromite is from about 0.5 to about 7; and,d. Recovering a stabilized aqueous alkali or alkaline earth metal hypobromite solution.

Abstract: Disclosed is a metal sulfide composition for use as a machining aid comprising 55.0% to 65.0% by weight of manganese, 29.0% to 36.0% by weight of sulfur, and greater than 2.0% to 10% by weight of iron. Also disclosed is a method of making the metal sulfide composition comprising mixing manganese, sulfur, and iron; initiating an exothermic reaction between the manganese and sulfur, wherein the iron component moderates and cools the exothermic reaction; forming a solid mass of manganese sulfide composition containing a portion of the iron suspended therein; and recovering the solid manganese sulfide composition. A method of using the manganese sulfide composition according to the present invention as a machining aid comprises mixing into a blend a desired metal powder with the manganese sulfide composition; spreading the blend into a metal part die; compacting the blend into the die; sintering the compacted part; and machining the sintered part.

Abstract: The invention is a method for preparing a stabilized aqueous alkali or alkaline earth metal hypobromite solution. The method comprises the steps of:a. Mixing an aqueous solution of alkali or alkaline earth metal hypochlorite with a water soluble bromide ion source;b. Allowing the bromide ion source and the alkali or alkaline earth metal hypochlorite to react to form a 0.5 to 30 percent by weight aqueous solution of unstabilized alkali or alkaline earth metal hypobromite;c. Adding to the unstabilized solution of alkali or alkaline earth metal hypobromite an aqueous solution of an alkali metal sulfamate having a temperature of at least 50.degree. C. in a quantity to provide a molar ratio of alkali metal sulfamate to alkali or alkaline earth metal hypobromite is from about 0.5 to about 6; and then,d. Recovering a stabilized aqueous alkali or alkaline earth metal hypobromite solution.

Abstract: Alkali metal quaternary chalcogenides and process for the preparation. The chalcogenides have the formula A.sub.x B.sub.y C.sub.z D.sub.n containing (CD.sub.4).sup.4- or (C.sub.2 D.sub.6).sup.4- ions where A is selected from the group consisting of an alkali metal and a mixture of alkali metals, B is selected from the group consisting of mercury, zinc and manganese, C is a metal selected from the group consisting of germanium and tin and D is selected from the group consisting of sulfur and selenium, wherein x, y, z and n are molar amounts which provide non-linear optical transmission properties. These chalcogenides are useful as non-linear optical transmission crystals.

Abstract: A chalcopyrite compound, for instance, CuInS.sub.2 or CuInSe.sub.2, is prepared by subjecting a thin film containing copper metal, indium metal, and an indium compound or a compound which contains both indium and copper, selected from the group consisting of oxides, sulfides and selenides, with heat under a reducing atmosphere containing at least one of the Group VIb element or under an atmosphere containing a reducing compound of at least one of the Group VIb element, thereby converting said thin film into a chalcopyrite compound.

Abstract: Alkali metal quaternary chalcogenides and process for the preparation. The chalcogenides have the formula A.sub.x B.sub.y C.sub.z D.sub.n containing (CD.sub.4).sup.4- or (C.sub.2 D.sub.6).sup.4- ions where A is selected from the group consisting of an alkali metal and a mixture of alkali metals, B is selected from the group consisting of mercury, zinc and manganese, C is a metal selected from the group consisting of germanium and tin and D is selected from the group consisting of sulfur and selenium, wherein x, y, z and n are molar amounts which provide non-linear optical transmission properties. These chalcogenides are useful as non-linear optical transmission crystals.

Abstract: Novel compound semiconductors are of the general formula, X.sub.5 YZ.sub.4, wherein X is a member selected from the group consisting of Cu, Ag and mixtures thereof, Y is a member selected from the group consisting of Al Ga, Tl and mixtures thereof, and Z is a member selected from the group consisting of Se, S, Te and mixtures thereof. Typical of the compound semiconductors are Cu.sub.5 AlSe.sub.4 and Ag.sub.5 AlSe.sub.4. These compound semiconductors are especially useful for making blue to UV light-emitting devices which include n-type and p-type compound semiconductor layers made of the above compound semiconductors.

Abstract: Disclosed are ceramic materials and methods of making the same comprising yttrium, barium, silver, and either selenium or sulfur. Those ceramic materials show changes in magnetic susceptibility at around 373.degree. K. with selenium and 195.degree. K. with sulfur.

Abstract: A composition for treating water that contains metal ions and possibly also organic and/or inorganic compounds is produced by reacting sulfur with an alkali- and/or alkaline earth metal hydroxide in the presence of water.The inventive composition corresponds to general formula IM.sub.x S.sub.y O.sub.z, (I)whereM represents an alkali or alkaline earth metal,x is 1 or 2,y is in the range 1.5x-2.5x, andz is in the range 0.1-2.5.

Abstract: A chalcopyrite-type compound, for instance, CuInS.sub.2 or CuGaS.sub.2, is prepared by subjecting a Group I-III oxide composition, containing at least one of the Group Ib element, for instance copper (Cu), and at least one of the Group IIIb element, for instance indium (In) or gallium (Ga) to a heat treatment under a reducing atmosphere containing the Group VIb element, for instance sulfur (S) or selenium (Se), or under an atmosphere containing a reducing compound of the Group VIb element, thereby converting said oxide composition into a chalcopyrite-type compound.