Abstract: In the conversion of a metal oxide to a metal chloride by reaction with chlorine and carbon monoxide wherein hydrogen chloride is produced as byproduct, the byproduct hydrogen chloride is contacted with a molten salt mixture containing the higher and lower valent chlorides of a multivalent metal and oxygen to recover the hydrogen chloride by enriching the salt in the higher valent metal chloride. Essentially all of the chlorine values are recovered from the salt by direct contact with all or a portion of the carbon monoxide fresh feed to the metal chloride production, with such carbon monoxide stripping gaseous chlorine from the salt, as well as combining with the chlorine to produce phosgene. The carbon monoxide, chlorine and phosgene are employed in the metal chloride production.

Abstract: A process is disclosed for recovering metallic constituents of spent or waste catalysts containing metallic compounds fixed on an aluminous support. The process is particularly applicable for the recovery of metals such as Al, Mo, V, Ni and Co, contained in spent catalyst. The process comprises transforming the metals to be recovered into volatile chlorides by carbochlorination and then separating the chlorides obtained by dry means and fixing them successively in a selective manner. The separation of AlCl.sub.3 is accomplished by passage through granules of anhydrous NaCl, and the separation of MoCl.sub.5 by passage through granules of crystallized KCl. The process is particularly suitable for the treatment of waste catalyst from the catalytic hydrocracking or hydrodesulfurization of oils.

Abstract: A process for forming a metal chloride of a metal or its compound comprising forming a liquid fused salt bath mixture of at least two metal chlorides, the bath having the property of dissolving the formed metal chloride, and introducing the metal or compound into the liquid fused salt bath in the presence of chlorine to form the metal chloride and recovering the formed chloride from the liquid fused salt bath mixture. The metals which may be chlorinated are those from groups 1b, 2a, 2b, 3a, 3b, 4a, 5a and 8 of the periodic table and the rare earth metals. Compounds from which the metals may be chlorinated are the sulfides, oxides, carbonates and sulfates. Chlorine may be introduced as such or its source may be a chlorine donor such as ferric chloride or sulfur chloride. The chlorides for the liquid fused salt bath are those of alkali metals, alkaline earth metals, ammonia, zinc, and ferric iron. The chlorination can be performed within a temperature range of 150.degree. C.-1000.degree. C.

Abstract: A method for the preparation of manganous chloride solutions using copper as a redox intermediate in the reaction between manganese and chlorine. Treatment of manganese-containing materials with a copper solution results in oxidation and dissolution of the manganese and the formation of elemental copper. The copper is in turn dissolved by reaction with cupric or ferric ions, which are then regenerated by chlorine oxidation.

Abstract: A process for preparing slightly soluble silver salt grains by mixing a solution or dispersion of a silver salt forming agent as a first liquid with a solution or dispersion of a silver ion-providing agent as a second liquid while controlling the electrode potential of the mixture of the first liquid and the second liquid using a measuring electrode and a reference electrode to produce the slightly soluble silver halide grains of specific characteristics depending upon the control of the electrode potential, the improvement which comprises the reference electrode comprising an internal electrode of a metal immersed in an internal solution of a metal salt of the metal of the internal electrode and an electrolyte, which metal salt and electrolyte do not release halide ions in the same liquid present as the major component in either of the first liquid or the second liquid.

Abstract: Improved rate of recovery of zinc values from the solids which are carried over by the effluent vapors from the oxidative vapor phase regeneration of spent zinc chloride catalyst is achieved by treatment of the solids with both hydrogen chloride and calcium chloride to selectively and rapidly recover the zinc values as zinc chloride.

Abstract: Ruthenium is stripped from a catalyst or electrode substrate by immersion in a fluoboric acid solution, converted to ruthenium oxide, and the ruthenium oxide is then converted to the alpha ruthenium trichloride for use in the preparation of fresh catalyst and/or electrodes.

Abstract: A tetrafluoromethane (CF.sub.4) generator and process is disclosed that facilitates the relatively low temperature production of CF.sub.4 gas via controlled decomposition of polytetrafluoroethylene (Teflon) and tetrafluoroethylene (C.sub.2 F.sub.4). CF.sub.4 produced via this process proves to be an excellent OH.sup.- scavenger in the processing and growth of metal fluoride single crystals.

Abstract: A process for making halogen salts which comprises reacting elemental halogen, hydrazine or a hydrazine compound, and a compound selected from the oxides and hydroxides of alkali metals, alkaline earth metals, Zn, Bi, Sn(II,IV), and Mn(II), the carbonates and bicarbonates of the alkali metals, alkaline earth metals, Sc, Y, Ti(IV), Zr, Hf, V(IV), Nb, Ta, Mn(II), Fe(II), Co(II), Ni, Cu(I), Ag, Zn, Cd, Hg(II), Al, Ga(III), Tl(III), Sn(II,IV), Pb(II) and Bi and the hydrates thereof, ammonia and ammonium compounds, such as ammonium carbonate, amines such as ethylenediamine, in the presence of a solvent medium selected from water, alcohols, ethers, and mixtures thereof. Thus, lithium carbonate, hydrazine, and elemental iodine react in water to produce lithium iodide which can be isolated from the water solution by evaporation.

Abstract: A hydrated metal salt is dehydrated to its anhydrous form by dissolving the metal salt hydrate in an organic solvent; and contacting the solvent solution of metal salt hydrate with a molecular sieve of a pore size sufficient to permit the absorption of water molecules but of a size too small to absorb solvent molecules.

Abstract: A process for purification of mercuric iodide (HgI.sub.2) to be used as a source material for the growth of detector quality crystals. The high purity HgI.sub.2 raw material is produced by a combination of three stages: synthesis of HgI.sub.2 from Hg and I.sub.2, repeated sublimation, and zone refining.

Abstract: Improved recovery of spent molten zinc halide hydro-cracking catalyst is achieved in the oxidative vapor phase regeneration thereof by selective treatment of the zinc oxide carried over by the effluent vapors from the regeneration zone with hydrogen halide gas under conditions favoring the reaction of the zinc oxide with the hydrogen halide, whereby regenerated zinc halide is recovered in a solids-free state with little loss of zinc values.

Abstract: This invention relates to reactions of beta platinum chloride with gaseous ammonia to yield metallic platinum useful in catalysis and other operations and also complexes of beta platinum chloride and ammonia, which complexes are considered to be new compositions and which are contemplated as being useful in cancer research.

Abstract: 9-Borabicyclo (3.3.1) noname (9-BBN), a relatively stable solid dialkylborane, can be used to reduce a wide variety of reducible chemical compounds, including both organic and inorganic compounds. The stability of the reagent greatly reduces the operating difficulties encountered with other dialkylboranes having similar reduction properties, which are thermally and hydrolytically unstable.

Abstract: This invention relates to reactions of beta platinum chloride with gaseous ammonia to yield metallic platinum useful in catalysis and other operations and also complexes of beta platinum chloride and ammonia, which complexes are considered to be new compositions and which are contemplated as being useful in cancer research.

Abstract: Hypochlorite ions in aqueous solution are catalytically decomposed by the action of a single-metal spinel of Co.sub.3 O.sub.4, preferably coated on an inert, stable support. The Co.sub.3 O.sub.4 catalyst may contain dispersed therein, optionally, other "modifier" metal oxides which do not affect the single-metal spinel structure of the Co.sub.3 O.sub.4, but which contribute better adherence of the Co.sub.3 O.sub.4 to the substrate and improve the toughness of the Co.sub.3 O.sub.4 coating.

Abstract: In a process for the recovery of metal chlorides from jarosite in sludges which result from the sulphuric acid processing of ores, the sludge is treated with an aqueous solution of an alkaline earth metal chloride. This solution contains free hydrochloric acid and is in excess stoichiometric ratio to the sulphate content of the sludge. The insoluble materials are separated from the metallic chloride solution by filtering, and are stripped of metallic chlorides by washing and further filtering. The metallic chloride solutions are then collected. The alkaline earth chloride is preferably calcium chloride. The process is particularly, but not exclusively, applicable to recovering metals from jarosite-type sludge resulting from the processing of zinc ore.

Abstract: Process for selectively recovering metal chlorides from a gaseous mixture of metal chlorides by contacting the gaseous mixture at a temperature above the condensation point of the mixture with at least one stream of liquid to cool all the mixture to below the freezing point of at least one metal chloride in the mixture, the average velocity of the mixture being at least the pneumatic conveyance velocity at the point of contact. This process provides for recovery of metal chlorides without plugging the apparatus.

Abstract: A process is disclosed for the preparation of arsenic trifluoride which comprises reacting arsenic trichloride with one or more molten fluoride salts.

Abstract: Anhydrous gold trichloride is prepared by stirring a suspension of finely divided tetrachloro-auric acid, having the thionyl chloride at a temperature in the range from 20.degree. to 65.degree. C in the absence of light, whereby said tetrachloro-auric acid and thionyl chloride react to form the desired end product.

Abstract: Trialkyl boranes are reacted with compounds containing protons in the presence of catalytic amounts of carboxylic acid derivatives, especially derivatives of t-alkyl carboxylic acids, thereby highly increasing the rate of protolyses of trialkyl boranes. These reactions may, for example, be utilized for the borylation of H-acidic compounds or for the dehydration of salts.

Abstract: Disclosed is a process for the recovery of antimony pentachloride from catalyst solutions used in the fluorination of chlorinated hydrocarbons characterized in that the exhausted catalyst solution containing antimony ions and high boiling halogenated hydrocarbons is chlorinated to convert the Sb.sup.3.sup.+ to Sb.sup.5.sup.+ followed by treatment of the solution with hydrogen fluoride to give SbCl.sub.x F.sub.y compounds, wherein x is 4-2 and y is 1-3, the sum of x+y being 5, and to convert the high boiling halogenated hydrocarbons to lower boiling halogenated hydrocarbons, thereafter removing the halogenated hydrocarbons having a lower boiling temperature than the boiling point of SbCl.sub.x F.sub.y and converting the remaining SbCl.sub.x F.sub.y compound with carbon tetrachloride to form antimony pentachloride which is thereafter separated from the remaining organic compounds and inorganic residue.

Abstract: This invention provides a halidation process for obtaining a high purity manganese oxide from a manganiferous ore, while reclaiming a substantial portion of the hydrogen halide reagent. The process comprises halidating the ore with a hydrogen halide and leaching to form the corresponding halogen and an aqueous solution comprising dissolved manganese halide and ferric halide. The hydrogen halide can be in the gaseous state and/or dissolved in the aqueous leach solution.The manganese halide and the ferric halide are preferably individually separated from the leach solution by crystallization and by selective extraction, respectively. The crystallized manganese halide is reacted with water at a temperature of from about 400.degree. C to about 700.degree. C to yield the corresponding hydrogen halide, which is recycled, and manganese oxide.In one embodiment, a concentrated leach solution is formed at a temperature of at least about 90.degree.

Abstract: A process is described for purifying liquids by cryogenic sublimation. This process involves solidifying the liquid by reducing the temperature and pressure to below the triple point. Purification is then carried out by direct transformation from the solid to the vapor phase. Because of increased differentials in vapor pressures at the low temperature at which the procedure is carried out, this purification process is highly efficient and is also particularly suitable for liquids that are susceptible to decomposition with ordinary purification procedures requiring elevated temperatures. The procedure is also advantageous in separating azeotropes, structurally similar compounds, as well as treating flammable, hydroscopic, corrosive and fuming compounds.

Abstract: A process for the recovery of precious metal values from ores whereby the ore, in particulate form is heated with a mixture of solid (dry) chloride and nitrate salts, in the absence of oxygen. The precious metal values are recovered in the form of the corresponding chlorides which are removed from the system by sublimation or vaporization. The chlorides of the precious metal values are then trapped, separated and can be reduced by conventional methods. Gold, silver and platinum are particularly amenable to recovery from complex ores by this method.

Abstract: A chemical process for treating metal sulfide materials, such as copper sulfide concentrates, to produce water-soluble metal chlorides and preclude the production of undesirable sulfur oxides. Such a metal sulfide material is contacted with an effective amount of a chlorinating reagent solution at a temperature below the boiling point of the reagent solution. The reaction proceeds until the metal sulfides are converted into metal chlorides and elemental sulfur is formed. The chlorinating reagent solution contains a chlorinating agent having a labile chlorine atom capable of reacting with the metal values to form metal chlorides, and at least one liquid hydrocarbon solvent which is capable of solubilizing both the chlorinating agent and the elemental sulfur produced during the reaction. The metal chloride product, which is insoluble in the reagent solution, is recovered from such solution by conventional means, e.g. by filtration, for conversion into the metal or metals.

Abstract: An improved process for the recovery of mercury from exhausted mercury-containing catalyst by heating the inactive catalyst at 270.degree.-600.degree.C. while passing a carrier gas therethrough, which comprises pretreating the exhausted catalyst with chlorine.

Abstract: Dimethylsulfoxide is used as a solvent for the growth of red mercuric iodide (HgI.sub.2) crystals for use in radiation detectors. The hygroscopic property of the solvent allows controlled amounts of water to enter into the solvent phase and diminish the large solubility of HgI.sub.2 so that the precipitating solid collects as well-defined euhedral crystals which grow into a volume of several cc.

Abstract: A method of recovering in highly pure states heavy metals such as cobalt, manganese, etc.

Abstract: This invention provides a process for obtaining substantially pure manganese metal by the reduction of a manganese oxide or a manganese halide by reaction with a subhalide of a transport metal. The transport metal can be aluminum, silicon, or titanium. In preferred embodiments of this procedure, a continuous closed cycle process is carried out wherein the transport metal value is reconverted to its subhalide and recycled for reaction with additional manganese compound.

Abstract: Antimony sulfide contained in an antimony sulfide bearing ore, such as stibnite, is converted to high purity antimony trichloride by reacting the antimony sulfide bearing ore with a source of chlorine to form high purity antimony trichloride and sulfur or hydrogen sulfide as separable by-products. The high purity antimony trichloride may be hydrolyzed to form high purity antimony oxide.

Abstract: This invention provides a process for separating metal values from an anhydrous mixture of metal halides in a fluid state, i.e. vapor or liquid; the separation is made by contacting a fluid mixture containing a halide of at least one less-noble metal selected from the group consisting of iron and manganese, and a halide of at least one more-noble metal selected from the group consisting of copper, cobalt and nickel, with an elemental metal. This procedure is especially effective in the refining of ocean floor nodule ores.

Abstract: A new process or method has been developed whereby the purity of metal halides, prepared by conventional methods, can be significantly upgraded. The process, which includes a scrubbing of metal halides with a halide-source species in the vapor phase, has been shown to be effective not only in reducing the concentration of oxyanion impurities and volatile cation halide impurities, but effective in reducing hydroxyl ion (OH.sup.-) contaminations as well.Metal halides purified by this method are particularly useful as starting materials for growing optically pure metal halide crystals.

Abstract: The process of this invention for the production of doped metal halides, especially silver halides, comprises reacting a doped metal with the vapour of the halogen in a closed vessel. A mono- or polycrystalline metal halide body is built up on a stationary or rotating base. Homogenously doped metal halides are obtained.