256results about "Germanium compounds" patented technology

A complex fluoride A2MF6 wherein M is a tetravalent element Si, Ti, Zr, Hf, Ge or Sn, A is an alkali metal Li, Na, K, Rb or Cs is prepared by providing a first solution containing a fluoride of M, providing a second solution containing a compound of A and / or the compound of A in solid form, mixing the first solution with the second solution and / or the solid for reacting the fluoride of M with the compound of A, and recovering the resulting solid product via solid-liquid separation.

A process for recovering lead oxides from the spent paste of exhausted lead acid batteries. The process provides heating the spent paste with an alkali hydroxide solution at elevated temperatures prior to calcinations. Calcination is at various temperatures so that either lead mono-oxide, lead dioxide or red lead is obtained as the principal product. There is also provided the use of the lead oxide to prepare the paste for positive and negative electrodes or other lead compounds.

A complex fluoride A 2 MF 6 wherein M is a tetravalent element Si, Ti, Zr, Hf, Ge or Sn, A is an alkali metal Li, Na, K, Rb or Cs is prepared by providing a first solution containing a fluoride of M, providing a second solution containing a compound of A and / or the compound of A in solid form, mixing the first solution with the second solution and / or the solid for reacting the fluoride of M with the compound of A, and recovering the resulting solid product via solid-liquid separation.

An outstandingly low environmental impact wet process recovers the lead content of an electrode slime and / or of lead minerals in the valuable form of high purity lead oxide or compound convertible to highly pure lead oxide by heat treatment in oven at relatively low temperature, perfectly suited for making active electrode pastes of new batteries or other uses. The process basically comprises the following treatments:a) suspending the impure lead containing material in an aqueous bath containing at least a lead oxide dissolving acid;b) reducing any insoluble lead dioxide to lead oxide by introducing in the suspension either hydrogen peroxide, a sulphite or sulphurous anhydride;c) converting all dissolved lead oxide to lead sulphate in the aqueous bath;d) obtaining a solution of lead sulphate obtained in an aqueous solution containing an acetate salt;e) precipitating and separating a purified lead compound in the form of either carbonate / oxycarbonate or of oxide / or hydroxide by adding to said acetate salt solution a carbonate salt or a hydroxide of the same cation of said acetate salt, respectively.Exemplary flow sheets according to several alternative embodiments and related processing plant diagrams are disclosed.

The present invention is a process of making a germanium-antimony-tellurium alloy film using a process selected from the group consisting of atomic layer deposition and chemical vapor deposition, wherein a silylantimony precursor is used as a source of antimony for the alloy film. Novel silylantimony compounds are also disclosed.

The present invention relates generally to metal oxide materials with varied symmetrical nanostructure morphologies. In particular, the present invention provides metal oxide materials comprising one or more metallic oxides with three-dimensionally ordered nanostructural morphologies, including hierarchical morphologies. The present invention also provides methods for producing such metal oxide materials.

There is provided a process for recovering high purity litharge PbO from spent lead acid battery paste at low temperatures and the further preparation of highly pure lead oxides and Pb(OH)2.

The disclosure relates to an electrode active material including: (a) first particulate of a metal (or metalloid) oxide alloyable with lithium; and (b) second particulate of an oxide containing lithium and the same metal (or metalloid) as that of the metal (or metalloid) oxide, and to a secondary battery including the electrode active material. When the electrode active material is used as an anode active material, reduced amounts of an irreversible phase such as a lithium oxide or a lithium metal oxide are produced during initial charge-discharge of a battery since lithium is already contained in the second particulate before the initial charge-discharge, and thus a dead volume on the side of the cathode can be minimized and a high-capacity battery can be fabricated.

The present invention provides novel compounds of the formula Gei-x-ySixSny, wherein 0.01<y<0.11, and 0.26<x<0.35, and semiconductor structures comprising such compounds. The present invention also provides novel semiconductor structures comprising silicon substrates, an SiGe buffer layer, and a Group III-V or II-VI active layer. The present invention also provides novel semiconductor structures comprising silicon substrates, an SiGe buffer layer, an SiGeSn template layer, and an SiGe, Ge, Group III-V, or Group II-VI active layer.

A process for the recovery of one or more metal values from a metal ore material comprising those of one or more values and a matrix material having a sulfur content wherein the sulfur is present in an oxidation-reduction state of zero or less comprisinga. forming particulates from particles of said ore and an inoculate comprising bacteria capable of at least partially oxidizing the sulfur content;b. forming a heap of said particulates;c. biooxidizing the sulfur content andd. recovering those one or more metal values.

The invention relates to a process for recovering the transition metal component of catalysts used in the hydroconversion of heavy hydrocarbonaceous materials. In accordance with the invention, a slurry of a transition metal catalyst and hydrocarbon is catalytically desulfurized resulting in a desulfurized product and a solid residue containing the transition metal. The transition metal may be recovered by coking the residue and then dividing the coker residue into two portions are combusted with the flue dust from the first combustion zone being conducted to the second combustion zone. The flue dust from the second combustion zone is treated with ammonia and ammonium carbonate in order to obtain ammonium molybdate.

The present invention describes a method of recycling lead from lead containing waste, the method comprising the steps of mixing the battery paste with aqueous citric acid solution so as to generate lead citrate; isolating lead citrate from the aqueous solution; and converting the lead citrate to lead and / or lead oxide.

Aqueous solutions containing lead, zinc and manganese are treated to recover these metals by sequential solvent extraction steps. Solvent extractants are selected to extract preferentially lead, then zinc and then manganese in that order. Any interfering metals are removed (as by ion exchange) before extraction. The loaded extractant phases are stripped with selected acids and lead, zinc and manganese each recovered from the strip solutions. Optionally calcium can be recovered when present. A preferred type of extractant (for lead especially) is substituted monothiophosphinic acids. A closed loop system is described which is advantageous with leachate from sulphide and carbonate ores.

Solvent extraction of one or more metal ions from an aqueous solution in the presence of hydrocarbon-soluble aminomethylenephosphonic acid derivatives.

A method for producing an indium oxide-tin oxide powder, which comprises supplying to react an aqueous solution of an indium salt, an aqueous solution of a tin salt and an aqueous alkaline solution into water at 40 DEG C. or more and less than 100 DEG C. so that the pH during the reaction is maintained within the range from 4 to 6, forming a precipitate, washing the formed precipitate after solid-liquid separation, and calcining the precipitate at 600 DEG C. or more and 1300 DEG C. or less.

Processes described include reacting a fresh or spent catalyst, or sorbent, with a solution containing an extracting agent (such as an acid or a base). Preferably, the catalyst contains both alumina and a molecular sieve (or a sorbent), and the reaction is performed under relatively mild conditions such that the majority of the base material does not dissolve into the solution. Thus, the catalyst can be re-used, and in certain instances the performance of the catalyst even improves, with or without re-incorporating certain of the metals back into the catalyst. Additionally, metals contained in the catalyst, such as Na, Mg, Al, P, S, Cl, K, Ca, V, Fe, Ni, Cu, Zn, Sr, Zn Sb, Ba, La, Ce, Pr, Nd, Pb, or their equivalent oxides, can be removed from the catalyst. Some of the metals that are removed are relatively valuable (such as the rare earth elements of La, Ce, Pr and Nd).

PCT No. PCT / FR96 / 01202 Sec. 371 Date May 27, 1998 Sec. 102(e) Date May 27, 1998 PCT Filed Jul. 30, 1996 PCT Pub. No. WO97 / 06215 PCT Pub. Date Feb. 20, 1997A method for preparing inorganic pigments from steel mill dust, particularly electric steel mill dust, wherein (a) the dust is separated into a magnetic fraction and a non-magnetic fraction; (b) the non-magnetic fraction is subjected to a basic leaching reaction; (c) the resulting solid batch is rinsed until neutralized and then separated; (d) the resulting batch is calcined at 450-650 DEG C.; (e) the calcined batch is treated with sulfuric acid in the presence of a catalyst; (f) the inorganic pigments are recovered; and (g) the solutions from (c) and (e) are used to precipitate other pigments.

Proposed is a method for collecting valuable metal from an ITO scrap in which a mixture of indium hydroxide and tin hydroxide or metastannic acid is collected by subjecting the ITO scrap to electrolysis in pH-adjusted electrolyte, and roasting this mixture as needed to collect the result as a mixture of indium oxide and tin oxide. This method enables the efficient collection of indium hydroxide and tin hydroxide or metastannic acid, or indium oxide and tin oxide from an ITO scrap of an indium-tin oxide (ITO) sputtering target or an ITO scrap such as ITO mill ends arisen during the manufacture of such ITO sputtering target.

A leaching composition that substantially removes lead from solid materials and a method of using said composition. Preferably, the concentration of lead in the solid materials following processing is low enough that the solid materials can be reused and / or disposed of at minimal cost to the processor. Preferably, the solid materials comprise glass, such as cathode ray tube glass.

The present invention provides novel compounds of the formula Gei-x-ySixSny, wherein 0.01<y<0.11, and 0.26<x<0.35, and semiconductor structures comprising such compounds. The present invention also provides novel semiconductor structures comprising silicon substrates, an SiGe buffer layer, and a Group III-V or II-VI active layer. The present invention also provides novel semiconductor structures comprising silicon substrates, an SiGe buffer layer, an SiGeSn template layer, and an SiGe, Ge, Group III-V, or Group II-VI active layer.

The invention discloses an alkaline earth metal germanate nanomaterial and a preparation method thereof and use of the nanomaterial as a cathode material of lithium ion batteries. The method comprises the following steps of: (1) mixing an aqueous solution of alkaline earth metal salt and germanium source compound GeO2 to obtain a liquid mixture; (2) allowing reaction of the liquid mixture obtained in the step (1) to take place in a polytetrafluoroethylene-lined high-pressure reaction kettle after heating, and cooling after the reaction is completed to obtain the alkaline earth metal germanate nanomaterial. The method is simple, has abundant and easily-available raw materials, is suitable for large-scale production and has a high level of practicability. The obtained alkaline earth metal germanate is a nanomaterial, has a high actual capacity, can be directly used as a cathode material of lithium ion batteries, solves the problem that the germanium-based material as lithium ion battery cathode material has a poor cycling property and takes a violent change of volume during charging / discharging process, and can be directly used as the cathode material of lithium ion batteries.

The invention pertains to a method for reducing the leaching of lead from lead projectile impact area acting to collect or stop such projectiles. The method includes contacting the lead projectile impact area with a seed of dry granular lead stabilizing agents. The seeding or coating of lead stabilizing agents provides a means to stabilize lead in the bullet / shot impact area while also allowing for future lead bullets, fragments, or lead shot fired into the soil to be stabilized upon contact with the lead stabilizing agent seeds or contact with rainwater leaching through the lead stabilizing agent seeds produced from the projectile coating, or excess seed from the lead shell projectiles. This method eliminates the need to remove or re-treat range soils and greatly reduces the environmental and health risks associated with the use of lead as projectiles in the open environment as well as at control trap ranges.

Provided is a method for preparing transition metal oxide nano-particles from a transition metal as a reactant. The method includes dissolving the transition metal into aqueous hydrogen peroxide to provide peroxi-metallate solution, and then adding a reactive solution containing an alcohol, water and an acid thereto to perform hydrothermal reaction. More particularly, the method for preparing transition metal oxide particles includes: dissolving transition metal powder as a reactant into aqueous hydrogen peroxide to provide a peroxi-metallate solution with a molar concentration of transition metal of 0.001-0.2 M; adding a reactive solution containing an alcohol, water and an acid to the peroxi-metallate solution to provide a mixed solution; and subjecting the mixed solution to hydrothermal reaction to provide transition metal oxide nano-particles.

A process for producing high purity lead oxide from impure lead compounds particularly from waste lead battery paste which includes an oxidation-reduction step. The process results in a reduction of impure lead compounds to the +2 valence state and metal particle contaminants are oxidized to the +2 state.

Disclosed is a method for making amorphous spherical particles of zirconium titanate and crystalline spherical particles of zirconium titanate comprising the steps of mixing an aqueous solution of zirconium salt and an aqueous solution of titanium salt into a mixed solution having equal moles of zirconium and titanium and having a total salt concentration in the range from 0.01 M to about 0.5 M. A stearic dispersant and an organic solvent is added to the mixed salt solution, subjecting the zirconium salt and the titanium salt in the mixed solution to a coprecipitation reaction forming a solution containing amorphous spherical particles of zirconium titanate wherein the volume ratio of the organic solvent to aqueous part is in the range from 1 to 5. The solution of amorphous spherical particles is incubated in an oven at a temperature ≦100° C. for a period of time ≦24 hours converting the amorphous particles to fine or ultrafine crystalline spherical particles of zirconium titanate.

Proposed is a method for collecting valuable metal from an ITO scrap including the steps of subjecting the ITO scrap to electrolysis in pH-adjusted electrolyte, and collecting indium or tin as oxides. Additionally proposed is a method for collecting valuable metal from an ITO scrap including the steps of subjecting the ITO scrap to electrolysis in an electrolytic bath partitioned with a diaphragm or an ion-exchange membrane to precipitate hydroxide of tin, thereafter extracting anolyte temporarily, and precipitating and collecting indium contained in the anolyte as hydroxide. With the methods for collecting valuable metal from an ITO scrap described above, indium or tin may be collected as oxides by roasting the precipitate containing indium or tin. Consequently, provided is a method for efficiently collecting indium from an ITO scrap of an indium-tin oxide (ITO) sputtering target or an ITO scrap such as ITO mill ends arisen during the manufacture of such ITO sputtering target.

Proposed is a method for collecting valuable metal from an ITO scrap including the steps of subjecting the ITO scrap to electrolysis and collecting the result as indium-tin alloy. Additionally provided is a method for collecting valuable metal from an ITO scrap including the steps of providing an ITO electrolytic bath and an indium-tin alloy collecting bath, dissolving the ITO in the electrolytic bath, and thereafter collecting indium-tin alloy in the indium-tin alloy collecting bath. These methods enable the efficient collection of indium-tin alloy from an ITO scrap of an indium-tin oxide (ITO) sputtering target or an ITO scrap such as ITO mill ends arisen during the manufacture of such ITO sputtering target.