Abstract: Organo clay and activated carbon are mixed to form a particle mixture. The particle mixture is contacted with waste water having chlorides and other contaminants, such as organic materials, heavy metals, chlorides, and low level radio nuclei in solution. Acids, oxidizing chemicals, and compressed air are added to pretreat and to treat the waste water. The mixture is filtered with catalytic activated carbon filters to remove the remaining contaminants. The filters produce a clean chloride solution that is discharged or is subjected to a finishing process to produce a marketable chloride product.

Abstract: A process for treating a mixed sulphidic material containing lead sulphide and at least one other metal sulphide. The process includes the steps of subjecting the mixed sulphidic material to selective oxidation such that lead sulphide in the material is oxidised to form an oxidized lead compound while substantial oxidation of the at least one other metal sulphide is avoided, and separating the oxidized lead compound from the at least one other metal sulphide. The oxidized lead compound may be separated by flotation wherein the oxidized lead compound reports to the tailings and the at least one other metal sulphide reports to the concentrate (froth).

Abstract: The present invention relates to the recovery of high purity litharge from spent lead acid battery paste at a low temperature which does not produce sulfur dioxide. In the process lead acetate or other lead salt is produced which is converted to high purity litharge by precipitation with a base.

Abstract: A process for treating a mixed sulphidic material containing lead sulphide and at least one other metal sulphide. The process includes the steps of subjecting the mixed sulphidic material to selective oxidation such that lead sulphide in the material is oxidised to form an oxidised lead compound while substantial oxidation of the at least one other metal sulphide is avoided, and separating the oxidized lead compound from the at least one other metal sulphide. The oxidized lead compound may be separated by flotation wherein the oxidized lead compound reports to the tailings and the at least one other metal sulphide reports to the concentrate (froth).

Abstract: There is provided a process for decontaminating and converting volumetrically contaminated radioactive metals, especially nickel, and recovering a decontaminated metal hydroxide or metal carbonate. The process includes the use of hydrogen peroxide to oxidize and remove nucleotides.

Abstract: Disclosed is a method for recycling lead from waste glass containing lead, which comprises the following steps: mechanical crushing waste glass containing lead, ball milling and screening to obtain glass powder containing lead; alkaline roasting the glass powder containing lead to obtain a roasted material; mixing polycarboxylic acid complexant and nitric acid to produce leaching agent, and then placing the roasted material into the leaching agent to obtain leachate; regulating pH value of the leachate to solidify metal ion to obtain precipitate, separating and removing impurities, rinsing and drying to obtain chemical product containing lead. The method avoids environment pollution caused by waste glass containing lead.

Abstract: There is described a process of recycling screen glass resulting from the disposal of cathode tube televisions, with quantitative recovery of lead in the form of sulphide and of silicates of cations other than lead, and subsequently recycling all the materials so recovered.

Abstract: A process for producing basic lead carbonate is provided. The process comprises: (1) immersing neutralization slag to obtain sodium hydroxide solution; (2) leaching lead chloride slag with the aqueous solution containing sodium chloride and hydrochloric acid, adding sodium sulfide and filtering; (3) neutralizing the filtrate with sodium hydroxide solution, filtering and washing the precipitate; and (4) converting the precipitate to basic lead carbonate with ammonium bicarbonate, crystallizing and washing. Said neutralization slag and lead chloride slag are the redundant slag from fire refining bismuth. Said process makes better use of the redundant slag from fire refining bismuth, saves resources and reduces environmental pollution.

Abstract: The present invention relates to the recovery of high purity litharge from spent lead acid battery paste at a low temperature which does not produce sulfur dioxide. In the process lead acetate is produced which is converted to pure litharge.

Abstract: Disclosed is a method for recycling lead from waste glass containing lead, which comprises the following steps: mechanical crushing waste glass containing lead, ball milling and screening to obtain glass powder containing lead; alkaline roasting the glass powder containing lead to obtain a roasted material; mixing polycarboxylic acid complexant and nitric acid to produce leaching agent, and then placing the roasted material into the leaching agent to obtain leachate; regulating pH value of the leachate to solidify metal ion to obtain precipitate, separating and removing impurities, rinsing and drying to obtain chemical product containing lead. The method avoids environment pollution caused by waste glass containing lead.

Abstract: A process for producing basic lead carbonate is provided. The process comprises: (1) immersing neutralization slag to obtain sodium hydroxide solution; (2) leaching lead chloride slag with the aqueous solution containing sodium chloride and hydrochloric acid, adding sodium sulfide and filtering; (3) neutralizing the filtrate with sodium hydroxide solution, filtering and washing the precipitate; and (4) converting the precipitate to basic lead carbonate with ammonium bicarbonate, crystallizing and washing. Said neutralization slag and lead chloride slag are the redundant slag from fire refining bismuth. Said process makes better use of the redundant slag from fire refining bismuth, saves resources and reduces environmental pollution.

Abstract: 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.

Abstract: A method of preparing basic metal carbonate selected from the group consisting of zinc carbonate, nickel carbonate, silver carbonate, cobalt carbonate, tin carbonate, lead carbonate, manganese carbonate, lithium carbonate, sodium carbonate, and potassium carbonate from metals comprising: contacting the metal with an aqueous solution comprising an amine, carbonic acid, and oxygen under conditions where the metal is converted into basic metal carbonate; and recovering the basic metal carbonate.

Abstract: A method for recovering a metal, capable of recovering a metal easily without requiring the use of an organic medium, is provided. A complex between a chelating agent and a metal present in a sample is formed in a mixture prepared by mixing the chelating agent and the sample under pH conditions where the chelating agent can be insoluble in an aqueous medium. Then, the complex is recovered from the mixture, and further, the metal is recovered by dissolving the recovered complex in an aqueous medium under pH conditions that are different from the pH conditions where the chelating agent can be insoluble in an aqueous medium. By this method, a metal can be recovered easily without requiring the use of the use of an organic medium.

Abstract: A method for recovering a metal, capable of recovering a metal easily without requiring the use of an organic medium, is provided. A first complex between a first chelating agent and a metal present in a sample is formed in a first mixture prepared by mixing the first chelating agent and the sample. Then, the first complex is recovered from the first mixture, and a second complex between the metal derived from the first complex and a second chelating agent is formed in a second mixture prepared by mixing the first complex and an aqueous solution of the second chelating agent. The aqueous solution is under the pH conditions where the first chelating agent can be insoluble in the aqueous solution. Then, a liquid fraction containing the second complex is recovered from the second mixture. Thus, the metal can be recovered.

Abstract: Uses for a composition comprising a polymer derived from at least two monomers: acrylic-x and an alkylamine, wherein said polymer is modified to contain a functional group capable of scavenging one or more compositions containing one or more metals are disclosed. These polymers have many uses in various mediums, including wastewater systems.

Abstract: Wet process of low environmental impact recovers the lead content of an electrode slime and/or of lead minerals in the valuable form of high purity-lead carbonates that are 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.

Abstract: Disclosed is a process for removing metals from waste, particularly electronic waste (or “e-waste”). The process generally includes the steps of dissolving at least some of the metals from the waste with nitric acid reagent and then causing at least some of the metals to precipitate as metal oxides and/or metal nitrates. NOx gases produced as by-product by the nitric acid dissolution of metallic components in the electronic waste are reused, in particular for generating permanganate when one of the metallic components comprises manganese.

Abstract: 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.

Abstract: Proposed is a method for collecting valuable metal from an ITO scrap including a step of collecting tin by subjecting the ITO scrap to electrolysis. Further proposed is a method for collecting valuable metal from an ITO scrap including the steps of providing an ITO electrolytic bath and a tin collecting bath, dissolving the ITO scrap in the electrolytic bath, and thereafter collecting tin in the tin collecting bath. Additionally proposed is a method for collecting valuable metal from an ITO scrap including the steps of dissolving the ITO scrap by subjecting it to electrolysis as an anode in electrolyte, precipitating only tin contained in the solution as tin itself or a substance containing tin, extracting the precipitate, placing it in a collecting bath, re-dissolving this to obtain a solution of tin hydroxide, and performing electrolysis or neutralization thereto in order to collect tin.

Abstract: 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.

Abstract: 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.

Abstract: A process for the recovery of a metal sulfide from a metal ion containing solution, including the steps of: a) providing a slurry containing seed panicles of said metal sulfide; h) adding a sulfide ion containing solution to said slurry to form an activated seed slurry; c) mixing said activated seed slurry with said metal ion containing solution to thereby form a metal sulfide precipitate; and d) recovering said metal sulfide precipitate.

Abstract: Disclosed is a method for producing, controlling the shape and size of, Pb-chalcogenide nanoparticles. The method includes preparing a lead (Pb) precursor containing Pb and a carboxylic acid dissolved in a hydrocarbon solution and preparing a chalcogen element precursor containing a chalcogen element dissolved in a hydrocarbon solution. The amount of Pb and chalcogen in the respective precursor affords for a predetermined Pb:chalcogen element ratio to be present when the Pb precursor is mixed with the chalcogen element precursor. The Pb precursor is mixed with the chalcogen element precursor to form a Pb-chalcogen mixture in such a manner that Pb-chalcogenide nanoparticle nucleation does not occur. A nucleation and growth solution containing a surfactant is also prepared by heating the solution to a nucleation temperature sufficient to nucleate nanoparticles when the Pb-chalcogen element mixture is added.

Abstract: 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.

Abstract: Provided is a process for producing fine particles of pure lead oxide from a waste lead oxide paste obtained from exhausted lead-acid batteries. The lead oxide particles so produced are substantially spherical and have a weight average particle size from about 13 nm to about 100 nm, which, are of nano-particle dimensions. The process according to the present invention is capable to produce pure lead oxide of PbO2 and lead oxide of Pb3O4 or commonly known as red lead.

Abstract: Wet process of low environmental impact recovers the lead content of an electrode slime and/or of lead minerals in the valuable form of high purity-lead carbonates that are 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.

Abstract: A method for treating a polymetallic sulfide ore containing gold and/or silver, and further containing base metals selected from the group consisting of iron, aluminum, chromium, titanium, copper, zinc, lead, nickel, cobalt, mercury, tin, and mixtures thereof, is disclosed. The method comprises the steps of grinding the polymetallic sulfide ore to produce granules, oxidizing the granules to produce oxidized granules, and chloride leaching the granules using a brine solution including dissolved halogens, as well as chloride and bromide salts.

Abstract: 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.

Abstract: The present invention relates to a desulfurization process of pastel and grids of lead accumulators comprising a carbonation in two steps, a granulometric separation between the two steps followed by specific desulfurization of the large part, a desodification obtaining the conversion of the PbSO4 contained in the pastel into PbCO3 which can be easily converted into metallic Pb in an oven by the addition of coal. The system used for the desodification of the large part of the pastel can also be used for the desulfurization of the fine part of the grids.

Abstract: A high temperature non-aqueous synthetic procedure for the preparation of substantially monodisperse IV-VI semiconductor nanoparticles is provided. The procedure includes introducing a first precursor selected from the group consisting of a molecular precursor of a Group IV element and a molecular precursor of a Group VI element into a reaction vessel that comprises at least an organic solvent to form a mixture. Next, the mixture is heated and thereafter a second precursor of a molecular precursor of a Group IV element or a molecular precursor of a Group VI element that is different from the first is added. The reaction mixture is then mixed to initiate nucleation of IV-VI nanocrystals and the temperature of the reaction mixture is controlled to provide nanoparticles having a diameter of about 20 nm or less.

Abstract: In a metal oxide nanoparticle and a synthetic method thereof, and in particular to maghemite (?-Fe2O3) nanoparticles usable as a superhigh density magnetic recording substance by having good shape anisotropy and magnetic characteristics, hematite (?-Fe2O3) nanoparticles usable as a precursor to the maghemite or a catalyst, maghemite and hematite-mixed nanoparticles and a synthetic method thereof, the method for synthesizing metal oxide nanoparticles includes forming a reverse micelle solution by adding distilled water, a surfactant and a solvent to metallic salt not less than trivalent, precipitating and separating gel type amorphous metal oxide particles by adding proton scavenger to the reverse micelle solution; adjusting a molar ratio of metal oxide to the surfactant by washing the gel type amorphous metal oxide particles with a polar solvent; and crystallizing metal oxide nanoparticles through heating or reflux after dispersing the gel type amorphous metal oxide particles in a non-polar solvent having a h

Abstract: A method of producing an Indium Tin Oxide powder is described. A method of producing an Indium Tin Oxide powder comprising the steps of: (1) mixing a raw aqueous solution containing indium ions and tin ions and having a proportion of divalent tin ions in the tin ions of 50 wt % or more with an alkali aqueous solution, (2) separating the product into solid and liquid, and (3) calcinating the resulted solid.

Abstract: 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.

Abstract: Nickel and lead ions are eliminated from an acidic concentrated iron(II) salt solution by adding an alkali sulfide and precipitating nickel and lead sulphides.

Abstract: Methods for sol-gel processing that generally involve mixing together an inorganic metal salt, water, and a water miscible alcohol or other organic solvent, at room temperature with a macromolecular dispersant material, such as hydroxypropyl cellulose (HPC) added. The resulting homogenous solution is incubated at a desired temperature and time to result in a desired product. The methods enable production of high quality sols and gels at lower temperatures than standard methods. The methods enable production of nanosize sols from inorganic metal salts. The methods offer sol-gel processing from inorganic metal salts.

Abstract: A solution method for preparing indium-tin oxide (ITO) powders is provided. Indium compounds and tin compounds are dissolved in water respectively to form two solution bodies. Some proper additives are added into the solution bodies to form metal hydroxyl compounds with determined composition. After water washing and filtration, proper additives are added into the solution to peptize the solution. During the peptization process, hydrolysis and condensation reactions occurs between different metal hydroxyl compounds. Solvent of the solution is then removed to form high quality nanometer grade ITO powders.

Abstract: Process for the manufacture of an aqueous sodium chloride solution, according to which a solid material comprising sodium chloride and heavy metals is dispersed in water, the aqueous medium thus obtained is alkalinized so as to precipitate the heavy metals in the form of metal hydroxides, calcium carbonate is coprecipitated with the metal hydroxides in the aqueous medium and the aqueous medium is then subjected to mechanical clarification.

Abstract: Ozone is used to rapidly oxidize specific metallic elements. The insoluble oxidized compounds of the metals formed by the ozonation are then recovered for industrial use in a conventional sedimentation/filtration tank or pool. There is no requirement for pre-treating or neutralizing the acid mine discharge, even when iron is the dominant metal. If the pH of the untreated acid mine discharge is less than about 2.5, metals other than iron precipitated first. After that, the pH is raised and the iron is precipitated as ferric hydroxide. Aluminum is removed as hydrated aluminum compounds after removal of the iron prior to discharging the acid mine discharge to streams. Both the ozonation and neutralization processes are monitored and controlled using electrochemical sensors and feedback controllers.

Abstract: A process for the separation of heavy metal and halogen from unwanted waste material or residue. Halogen is selectively extracted or washed out from the waste material. Metal is selectively extracted or washed out from the essentially halogen free waste material.

Abstract: A method for selectively separating and recovering palladium from an aqueous palladium/tin catalyst solution. The method includes the steps of adjusting the pH of the aqueous solution to a specified pH range thereby precipitating the tin, and producing a soluble form a palladium. The solution can be either pre-filtered or settled and subsequently processed through ion exchange resin in a conventional manner, or processed in an upflow direction through an at least partially fluidized bed of ion exchange resin to remove and concentrate the palladium for recovery.

Abstract: A sol-gel process for fabricating bulk, germanium-doped silica bodies useful for a variety of applications, including core rods, substrate tubes, immediate overcladding, pumped fiber lasers, and planar waveguides, is provided. The process involves the steps of providing a dispersion of silica particles in an aqueous quaternary ammonium germanate solution—typically tetramethylammonium germanate, gelling the dispersion to provide a gel body, and drying, heat treating, and sintering the body to provide the germanium-doped silica glass.

Abstract: A method and apparatus for removing metal contaminants from the spent salt of a molten salt oxidation (MSO) reactor is described. Spent salt is removed from the reactor and analyzed to determine the contaminants present and the carbonate concentration. The salt is dissolved in water, and one or more reagents may be added to precipitate the metal oxide and/or the metal as either metal oxide, metal hydroxide, or as a salt. The precipitated materials are filtered, dried and packaged for disposal as waste or can be immobilized as ceramic pellets. More than about 90% of the metals and mineral residues (ashes) present are removed by filtration. After filtration, salt solutions having a carbonate concentration >20% can be spray-dried and returned to the reactor for re-use. Salt solutions containing a carbonate concentration <20% require further clean-up using an ion exchange column, which yields salt solutions that contain less than 1.0 ppm of contaminants.

Abstract: A suede-like stitchbonded fabric is disclosed. The stitchbonded fabric includes a nonwoven substrate. A first yarn is stitchbonded into the substrate in a manner that forms loops at the surface of the substrate. A second yarn is then also stitchbonded into the substrate in order to secure the loops to the fabric. Thereafter, the fabric is abraded for substantially breaking all of the loops at the surface of the fabric.

Abstract: A method for treating residues derived from garbage and/or industrial waste incineration fumes including the steps of desalting the residues by washing with sodium carbonate in sufficient amount or slightly in excess to solubilize all the salts including the sulphates and precipitate the soluble calcium, the pH being higher than 11, then carrying out a solid/liquid separation to obtain a desalinated cake; leaching the desalinated cake with sodium carbonate in sufficient amount or slightly in excess to obtain, by reaction with the lime present in the cake or added thereto if necessary, the alkalinity required for solubilising amphoteric metals, the pH being higher than 12, and obtaining by solid/liquid separation a cake and a supernatant which is neutralised with carbon dioxide, and filtering the recovered solution to obtain metal hydroxide sludge and an aqueous sodium carbonate solution; and neutralising the resulting residues at a pH between 6.5 and 8.5.

Abstract: A process for preparing a nanocrystalline material comprising at least a first ion and at least a second ion different from the first ion, and wherein at least the first ion is a metal ion, is described. The process comprises contacting a metal complex comprising the first ion and the second ion with a dispersing medium suitable to form the nanocrystalline material and wherein the dispersing medium is at a temperature to allow formation by pyrolysis of the nanocrystalline material when contacted with the metal complex.

Abstract: The present invention provides both reagents and a process for removing heavy metals from a caustic fluid stream by the addition of reagents which are not corrosive or deleterious. Specifically, the present invention is directed to removing heavy metals from a Bayer liquor in an aluminum processing plant. The reagents, dithiocarbamate and dithocarbonate groups, are added individually or in combination thereof to the Bayer liquor for the removal of heavy metals, such as zinc. The reagents form a complex with the heavy metal for the precipitation of the metal from the fluid stream. Once a complex is formed, the Bayer liquor is held in a quiescent state for a period of time sufficient for settling out of solution the precipitate. After settling out of solution, the precipitate is separated and removed and the Bayer liquor is then further processed into alumina.

Abstract: The present invention relates to a process for treating fly ash/APC residues chlorides, sulphates, earth alkali metals selected from the group consisting of calcium, potassium, and sodium, and heavy metals selected from the group consisting of lead, which residues are obtained from air pollution control processes that utilize dry/semi-dry line injection, such that said residues may be disposed of as non-hazardous materials. The process comprises the sequential steps of: (a) washing and agitating the fly ash/APC residue (20) with water (50) to form a residue slurry containing solubilized lead salts and calcium chloride; (b) filtering (42) the residue slurry to remove a filtrate (46) having a pH of higher than about 11.8 and containing the solubilized lead salts and calcium chloride; and (c) recovering a first calcium enriched filter cake (44).

Abstract: A method is disclosed for recovering and separating precious and non-precious metals from waste streams, which removes, separates, and recovers such metals in a cost effective manner with more than 95% removal from waste streams and with minimal amounts of unprocessed solids and sludge remaining in the environment. Metals such as chromium, manganese, cobalt, nickel, copper, zinc, silver, gold, platinum, vanadium, sodium, potassium, beryllium, magnesium, calcium, barium, lead, aluminum, tin; and the like are removed and recovered from the waste streams with at least 95% removal and other metals and compounds, such as antimony, sulfur, and selenium are removed and recovered from waste streams with at least 50% removal. The method employs a unique complexing agent comprising a carbamate compound and an alkali metal hydroxide which facilitates the formation of the metals into ionic metal particles enabling them to be readily separated, removed and recovered.

Abstract: A process for preparing a nanocrystalline material comprising at least a first ion and at least a second ion different from the first ion, and wherein at least the first ion is a metal ion, is described. The process comprises contacting a metal complex comprising the first ion and the second ion with a dispersing medium suitable to form the nanocrystalline material and wherein the dispersing medium is at a temperature to allow formation by pyrolysis of the nanocrystalline material when contacted with the metal complex.