Abstract: A process for production of a borohydride compound M(BH4)y. The process has three steps. The first step combines a compound of formula (R1O)yM with aluminum, hydrogen and a metallic catalyst containing at least one metal selected from the group consisting of titanium, zirconium, hafnium, niobium, vanadium, tantalum and iron to produce a compound of formula M(AlH3OR1)y, wherein R1 is phenyl or phenyl substituted by at least one alkyl or alkoxy group; M is an alkali metal, Be or Mg; and y is one or two; wherein the catalyst is present at a level of at least 200 ppm based on weight of aluminum. The second step combines the compound of formula M(AlH3OR1)y with a borate, boroxine or borazine compound to produce M(BH4)y and a byproduct mixture containing alkali metal and aluminum aryloxides. The third step separates M(BH4)y from the byproduct mixture.

Abstract: Processes for recovering ammonia from an ammonium sulfate stream include reacting the ammonia sulfate stream with a lime slurry to form a slurry comprising calcium sulfate and ammonia; providing the slurry comprising calcium sulfate and ammonia to a stripper configured to recover the ammonia from the slurry; utilizing a heat source from a chilled ammonia process to the stripper; and extracting an ammonia vapor stream from the stripper. Also disclosed are systems for performing the processes.

Abstract: The present invention is a process for desulfurizing hydrocarbon feedstreams with alkali metal compounds and regenerating the alkali metal compounds via the use of a copper sulfide reagent. The present invention employs the use of a copper sulfide reagent to convert alkali metal hydrosulfides in the generation or regeneration of the alkali hydroxide compounds which may be utilized in a desulfurization process for hydrocarbon feedstreams. Additionally, in preferred embodiments of the processes disclosed herein, carbonates which form as byproducts of the desulfurization process, and are non-regenerable with copper sulfide, are removed from the alkali hydroxide stream.

Abstract: Multi-step metal compound oxidation process to produce compounds and enhanced metal oxides from various source materials, e.g. metal sulfides, carbides, nitrides and other metal containing materials with metal oxides from secondary reaction steps being utilized as an oxidation agent in the first reactions.

Abstract: A method of making a cesium salt is described and involves reacting a cesium sulfate containing solution with lime to form 1) a solution containing at least cesium hydroxide and 2) a residue comprising calcium sulfate. The method further involves removing the residue from the solution and converting the cesium hydroxide that is present in the solution to at least one type of cesium salt. The present invention further relates to uses of the cesium salt as well as methods of making cesium hydroxide using lime. Also, methods of making alkali metal salts and alkali metal hydroxides are also described.

Abstract: The present invention provides an inexpensive process for the preparation of lithium salts of formula LiX having a desired or required level of purity using lithium chloride and lithium sulfate. In the process of the invention, a lithium salt selected from lithium chloride, lithium sulfate, and combinations thereof is reacted with NaX or KX in a aqueous, semiaqueous, or organic solution and the precipitated salts are removed to obtain the LiX solution of desired purity. Preferably, a semiaqueous solution containing water and an organic solvent is used at some point in the reaction. The process of the invention eliminates the use of highly acidic materials and thus reduces the cost of raw materials and the need for specialized equipment.

Abstract: Aluminum polychlorosulphates having the general formula (I) Al(OH)l Clm(SO4)nMp(I) where M represents an alkali metal l, m, n, p represent the number of moles per mole of aluminum, so that 1.74≦l≦2.25, 0.01≦n≦0.17, 0.32≦p≦1.49, and l+m+2n=p+3, their use as coagulation and flocculation agents, and their preparation process by reaction, at room temperature, of an alkali metal basic compound, such as Na2CO3, NaHCO3, NaOH, K2CO3, KHCO3 and KOH, and an alkali metal sulphate or sulphuric acid with an aluminum polychloride or polychlorosulphate having the general formula(I′) Al(OH)l′Clm′(SO4)n′Mp′(I′) where 1.1≦1′≦1.44, n′≦0.10, p′<p(p of formula (I)), and l′+m′+2n′=p′+3.

Abstract: A method of making a cesium salt is described and involves reacting a cesium sulfate containing solution with lime to form 1) a solution containing at least cesium hydroxide and 2) a residue comprising calcium sulfate. The method further involves removing the residue from the solution and converting the cesium hydroxide that is present in the solution to at least one type of cesium salt. The present invention further relates to uses of the cesium salt as well as methods of making cesium hydroxide using lime. Also, methods of making alkali metal salts and alkali metal hydroxides are also described.

Abstract: Sulfur compounds present as sulfides and mercaptans in spent caustic streams from refinery and petrochemical processes are oxidized by contacting them with an oxygen-containing gas in a packed column recycle reactor.

Abstract: A process of preparation capable of easily preparing cathode materials having a homogeneous composition in a good mass productivity, a cathode material obtained by this process, and a secondary lithium ion battery using the cathode material. Aqueous solutions of each of a lithium salt, a transition metal salt, and a complexing agent are prepared and mixed in a stoichiometric ratio of a cathode material, and therefrom water is removed by spray-drying to give a precursor which is then sintered. High performance secondary lithium ion batteries are obtained by using the obtained cathode material in the positive electrode.

Abstract: A method for preparing an active substance for use in a positive electrode in chemical cells comprising a negative electrode is described. The method comprises preparing a mixed aqueous solution of a water-soluble lithium compound, a water-soluble transition metal compound, and an organic acid selected from the group consisting of organic acids having, in the molecule, at least one carboxyl group and at least one hydroxyl group and organic acids having at least two carboxyl groups, preparing an organic acid complex comprising lithium and a transition metal, and thermally decomposing the complex at temperatures sufficient for the decomposition to obtain the active substance. The complex may be prepared by dehydrating the solution. Alternatively, the complex may be formed by spraying the solution under heating conditions.

Abstract: A method for the recovery of chemical values from spent lignocellulosic pulping liquor salts to produce white liquor of different sulfidities. Preferably, the white liquor is in the form of separate liquid streams, each of which is of a sulfidity that is different from the sulfidity of others of the streams. The method also provides for developing a white liquor stream which is essentially free of sulfide values, but which contains sodium hydroxide. Further, the method provides for recovery of titanium values for recycling.

Abstract: A method for preparing an active substance for positive electrode in non-aqueous electrolytic secondary cells making use of a lithium or lithium alloy negative electrode is described. The method comprises providing an amorphous citrate complex of lithium and a transition metal and firing the complex at a predetermined temperature to obtain an active substance. The citrate complex is obtained by preparing an aqueous mixed solution of lithium hydroxide or carbonate, a water-soluble transition metal salt and citric acid and dehydrating the mixed solution to obtain an amorphous citrate complex. The complex is then fired at a temperature ranging from 300.degree. to 900.degree. C. to obtain an active substance.

Abstract: The present invention is directed toward a process for regenerating sodium hydroxide (NaOH) from aqueous solutions of sodium sulfide (Na.sub.2 S) comprising heating aqueous sodium sulfide in the presence of a metal selected from the group consisting of iron and cobalt, for a time and at a temperature sufficient to form a metal sulfide, sodium hydroxide and molecular hydrogen.

Abstract: The invention relates to a process for the preparation of an essentially sulfide-free alkali liquor starting from a pulp mill alkali sulfide source, characterized by reacting in alkaline medium the alkali sulfice source with copper (II) oxide and/or copper (I) oxide, optionally with the addition of water, in a mole ratio oxide to sulfide (calculated as alkali sulfide) (charging) of at least 0.9 and allowing the mixture obtained to react at a temperature of from 30.degree. to 130.degree.0 C. to form hydroxide in an amount equivalent to the amount of sulfide and to precipitate a solid phase consisting essentially of copper (I) sulfide, copper (II) sulfide or a mixture thereof, whereupon the solid phase is separated in a way known per se to obtain an essentially sulfide-free alkali liquor, the reaction time of the precipitation reaction being adjusted with regard to the charging and temperature selected so that the residual concentration of copper ions in the final alkali liquor is below 1 mmole/l.

Abstract: A method of treating an aqueous sodium sulfide solution, such as white liquor in kraft pulping systems, for the oxidation of the sulfide with oxygen in the presence of a specific activated carbon catalyst which is (a) a particulate activated carbon catalyst having an average particle diameter of 0.2-4 mm, a pore volume of at least 0.25 cc/g in pores with diameters of not smaller than 100 .ANG. and a pore volume of at least 35% of the total pore volume in pores with diameters of not smaller than 100 .ANG. or (b) a fibrous activated carbon catalyst having a specific surface area of 300-2500 m.sup.2 /g and an outer surface area of 0.1-5 m.sup.2 /g.

Abstract: A continuous process for the manufacture of a metal salt solution is described which provides more economical products with higher quality than current processes. The process is safer, both to operating personnel and to the environment, than currently used processes. The process comprises feeding an aqueous metal compound slurry, e.g., a metal oxide/hydroxide slurry and a mineral acid, e.g., nitric acid, and water to a reactor which includes a zone of extreme mixing and agitation, most preferably a cross-pipe reactor provided with an optional static in-line mixer. A cross-pipe reactor provides complete and efficient reaction by providing greater surface area, high agitation and a long reaction time.

Abstract: H.sub.2 S and CO.sub.2 from a waste gas are absorbed in an ammoniacal or alkali metal hydroxide solution. The resultant sodium, potassium or ammonium sulfide solution is reacted with pulverized copper oxide and the resultant copper sulfide precipitate is separated and the resultant solution of increased sodium hydroxide, potassium hydroxide or ammonia content is recycled as absorbent for hydrogen sulfide and CO.sub.2. The copper sulfide is roasted to form recyclable copper oxide and product sulfur dioxide.

Abstract: Sodium sulfide or sodium hydrosulfide is oxidized to form sodium polysulfide and sodium hydroxide which may be further oxidized to sodium thiosulfate and sodium hydroxide. The oxidant is air, oxygen or oxygen in mixture with other gases, the reductant is aqueous sodium sulfide or sodium hydrosulfide and the reaction is carried out with both reactants in non-flooded contact with a solid catalyst material, of which a typical example is a particulate carbon treated with polytetrafluoroethylene (PTFE). The reaction is typically conducted at atmospheric pressure and without the application of heat, with the oxidant and the reductant being in interfacial contact with each other, but only, insofar as possible, at sites where both are simultaneously in contact with a catalyst which is prevented from being flooded by either the oxidant or reductant.

Abstract: A method and composition are described for the decomposition of sodium-mercury amalgam in a reactor containing solid packing particles to form hydrogen, sodium hydroxide, and denuded mercury. The novel packing particles are comprised of a heterogeneous solid mixture of a matrix of a thermally stable polymer having embedded therein discrete particles of a surface active composition. Suitable thermally stable polymers include polyphenylene sulfide and suitable surface active compositions include carbon, iron, nickel, cobalt, vanadium, and molybdenum. The proportion of the polymer in the packing generally ranges from about 20 to about 80 percent by volume. Preferably, the matrix is prepared in porous form which may also be coated with a surface active metal.

Abstract: Sodium polysulfide is prepared by the oxidation of sodium sulfide or sodium hydrosulfide, and by using new procedures and systems described, the production of thiosulfate can be markedly reduced and, in some cases, eliminated. The oxidant is air, oxygen or oxygen in mixture with other gases, the reductant is aqueous sodium sulfide or sodium hydrosulfide and the reaction is carried out with both reactants in non-flooded contact with a solid catalyst material, of which a typical example is a particulate carbon treated with polytetrafluoroethylene (PTFE). The reaction is typically conducted at atmospheric pressure and without the application of heat, with the oxidant and the reductant being in interfacial contact with each other, but only, insofar as possible, at sites where both are simultaneously in contact with a catalyst which is prevented from being flooded by either the oxidant or reductant. Sodium polysulfide and sodium hydroxide are produced, and are useable in treatment of lignocellulose materials.