Abstract: Disclosed is a process, which is used to eliminate heavy metal cations from the aqueous media, and provides a better solution for the existing problems of the separation systems like low efficiency and high costs. The heavy metal cations selected for this purpose are cadmium, lead and copper. The separation system consists of a two stage process: In the first stage, the iron oxide nanoparticles are suspended in an aqueous medium contaminated with the heavy metal cations. In the second stage, the solution is brought into contact with a ferromagnetic matrix (or a paramagnetic matrix) magnetized by the application of an outside magnetic field. The heavy metal cations are deposited on the matrix under the imposed magnetic field. This two-stage process makes it possible to separate the heavy metal cations from the aqueous medium. The wire matrices are upon the completion of separation washed away by water or air current.

Abstract: Metal complexing agents are used to purify polymers including conducting polymers to provide very low metal content. The process comprises precipitating the polymer in solution into a solvent system comprising the metal complexing agent. Very low levels including undetectable levels of metals such as nickel and magnesium can be achieved. High purity polymers are used in electronics and photovoltaic applications.

Abstract: The present invention relates to an organo-ceramic composite material useful for the extraction of metal ions from solution. The organo-ceramic composite material is formed according to a sol gel synthesis scheme by reacting a functional precursor silane and its homopolymers with either (i) a mixture of a cross-linking silane and its homopolymers or (ii) the cross-linking silane, under conditions effective to yield the composite material of the present invention. Further aspects of the present invention relate to methods of removing a metal ion from a water stream and recovering a metal ion from a water stream, both of which include contacting a water stream containing a metal ion with an organo-ceramic composite material of the present invention under conditions effective to remove the metal ion from the water stream.

Abstract: There are provided methods and processes that employ a mercury-adsorbing granular material as a sorbent to remove mercury from fluids. The fluids can be waste fluids that result from manufacturing, processing, or other treatment processes or systems. The fluids can also be fluids that are treated in their natural state. The fluids to be treated may include water, air, sludge, slurries, gases from processing or furnaces flues, gaseous flows, liquid flows, and other gases and liquids. In one excellent form of the invention, the mercury-adsorbing material includes taconite tailings.

Abstract: An apparatus for use in the treatment of contaminated fluid is provided. The apparatus includes an outer element into which contaminated fluid flows and an inner element positioned in substantial axial alignment within the outer element and in spaced relations thereto. The apparatus also includes, between its ends, a pathway defined by an interior surface of the inner element and along which treated fluid may be directed out from the apparatus. A waste nanoadsorbent material can be provided between the outer element and the inner element, for use in removing contaminants within the fluid flowing through the apparatus. A method for the treatment of contaminated fluid is also provided.

Abstract: Media for selectively removing radium ions from water where manganese oxide (DMO) has been dispersed in a cation ion exchange resin (gel or macroporous) to adsorb radium ions. The media is manufactured by precipitating a soluble manganese (II) salt such as manganous sulfate with a permanganate salt such as sodium permanganate inside a strong acid cation (SAC) to form a resin containing highly dispersed manganese oxides. The resin is then post treated with a reducing agent such as sodium metabisulfite (Na2S2O2) to prevent the leaching of soluble manganese from the resin. The reducing treatment ensures that soluble manganese species will be converted into an insoluble oxide form.

Abstract: A personally portable water purification compound prepared in unit dosage form such as tablets, packages and the like and having titanium dioxide (TiO2) in the form of fine particles, and adsorbed chlorine held at the surface of the titanium dioxide particles; and a titanium based coagulant; the compound being prepared in a plurality of unit dose size packages, for personal use by individuals. Also disclosed is a method of preparing a personally portable water purification compound consisting of the steps of heating titanium dioxide particles up to a temperature between about 260-500° C., passing a cold dry gaseous chlorine flow around the titanium dioxide particles; and cooling the titanium dioxide during the treatment.

Abstract: A water treatment composition includes an oxidizing component and an adsorbing component, wherein one or both of the oxidizing component and adsorbing component comprise nanostructured materials. The water treatment compositions are useful in at least partially removing contaminants such as metallic or cationic arsenic, lead, chromium, and/or mercury from water.

Abstract: The present invention is directed to a fuel supply and fuel system with an ion filter and an ion gauge. The filter can be made from discrete pieces of polymeric filter material. The polymeric filter material is substantially the same as the proton exchange membrane or polymer electrolyte membrane (PEM) in the fuel cell. The ion gauge measures the level of ions in the fuel by measuring a voltage across a section of fuel or a current through the same section. The voltage or current is related to the ion level in the fuel.

Abstract: An adsorbent for removal of impurities from silicone based solvents is presented. The adsorbent is regenerable for repeated use in cleaning silicone based solvents.

Abstract: Toxic substances such as heavy metals are extracted from a medium using a sorbent composition. The sorbent composition is derived by sulfidation of red mud, which contains hydrated ferric oxides derived from the Bayer processing of bauxite ores. Exemplary sulfidizing compounds are H2S, Na2S, K2S, (NH4)2S, and CaSx. The sulfur content typically is from about 0.2 to about 10% above the residual sulfur in the red mud. Sulfidized red mud is an improved sorbent compared to red mud for most of the heavy metals tested (Hg, Cr, Pb, Cu, Zn, Cd, Se, Th, and U). Unlike red mud, sulfidized red mud does not leach naturally contained metals. Sulfidized red mud also prevents leaching of metals when mixed with red mud. Mixtures of sulfidized red mud and red mud are more effective for sorbing other ions, such as As, Co, Mn, and Sr, than sulfidized red mud alone.

Abstract: A composition of matter wherein the composition comprises a siliceous substrate having silanols on the surface and a polymer selected from the group consisting essentially of a water soluble polymer, a water soluble copolymer, an alcohol soluble polymer, an alcohol soluble copolymer, and combinations of such polymers, wherein the polymer is chemically bonded to the siliceous substrate by a silane linking material having the general formula O3/2SiQY that is derived from an alkoxy-functional silane having the general formula (RO)3SiQX and processes for preparing the crosslinked polymer that is chemically bonded to the surface of the siliceous substrate.

Abstract: A runoff water filter is defined by an elongate, tubular mesh container filled with a filter medium that is selected for the ability of the filter medium to remove target pollutants from the runoff water. In a first disclosed embodiment, vermiculite is used as the primary filter medium for its ability to bind cationic compounds, principally zinc, from water running off metal buildings. Other filter media may also be employed to remove other target pollutants.

Abstract: A method for reducing barium concentration in waste streams. Hydrous manganese oxide (HMO) is formed in solution/slurry and mixed with water containing barium such that the hydrous manganese oxide exhibits a negative charge at a desired pH. Barium from the water is adsorbed onto the negatively charged HMO surface. The HMO with adsorbed barium is separated from the water, producing treated effluent having a reduced barium concentration.

Abstract: Embodiments herein provide waste abatement apparatuses and methods for treating waste solutions derived from depleted or used plating solutions, such as from an electroless deposition process or an electrochemical plating process. The waste abatement systems and processes may be used to treat the waste solutions by lowering the concentration of, if not completely removing, metal ions or reducing agents that are dissolved within the waste solution. In one embodiment of a demetallization process, a waste solution may be exposed to a heating element (e.g., copper coil) contained within an immersion tank. In another embodiment, the waste solution may be exposed to a catalyst having high surface area (e.g., steel wool or other metallic wool) within an immersion tank. In another embodiment, the waste solution may be flowed through a removable, catalytic conduit (e.g., copper tubing) having an internal catalytic surface.

Abstract: A method and apparatus are described for removing iron cations and/or zinc cations from an autodeposition coating bath by passing a limited number of bed volumes through a column containing a gel type SAC IEX resin when iron cations are to be removed and passing a substantially larger number of bed volumes through the column when zinc cations are to be removed. To prevent clogging when zinc cations are being removed the direction of the flow through the column is periodically reversed.

Abstract: The present invention provides a method of reducing the concentration of an iodide compound using an ion exchange resin. The ion exchange resin is a macroporous resin having sulfur functional groups exchanged with silver, a dry weight capacity of at least 5.0 eq/kg, a mean pore diameter (D50) of about 400-800 ?, a pore volume of about 0.4-0.6 ml/g, and a surface area of about 20-40 m2/g.

Abstract: The invention relates to a method for inhibiting the biological acidification of water which is in contact with materials containing sulfur in reduced form or with elemental sulfur, susceptible to oxidation on the part of Thiobacilli, comprising putting said materials in contact with soluble inorganic salts at concentrations ranging from 0.4 normal to saturation.

Abstract: The invention relates to new compounds of Formula 1: [(O3/2)Si CH2CH2SX]a [Si(O4/2)]b[Si(O3/2V)]C wherein X is selected from CH2A,[CH2CH2NR1]pR2, CHCOX1CH2COX2,(CH2)eCO Y[(CH2)eSCH2CH2Si(O3/2)]m[CO2(CH2)eSH]n wherein A is the residue of an amino acid or derivative or salt of an amino acid of formula CHNR1R2COX3; R1 and R2 are independently selected from hydrogen, C1-20alkyl, and C1-20alkylaryl C1-12acyl R is selected from hydrogen, metal ion, C1-5alkyl, P is 1 to 100 and e is 1 or 2; X1 and X2 are independently selected from OR and NR1R2; X3 is selected from OR, NR1R2 or known amino acids and proteins or derivatives thereof; and Y is the residue of polyol having z or fewer hydroxyl groups substituted and m+n+1 is less than or equal to z; the free valences of the silicate oxygen atoms are saturated by one or more of silicon atoms of other groups of Formula 1, hydrogen, a linear or branched C1-12-alkyl group or by end groups R33M1O1/2 or by cross-linking bridge members or by polymer chains R3qM1(OR4)gOk/2 or AI

Abstract: The present invention relates to a process for removing dissolved metal ions from an onium hydroxide and/or salt solution, including providing a weak acid ion exchange medium; providing a solution comprising magnesium ions; forming a magnesium-loaded ion exchange medium by contacting the ion exchange medium with the solution comprising magnesium ions; contacting the magnesium-loaded ion exchange medium with an onium hydroxide and/or salt solution containing a first quantity of dissolved metal ions, wherein at least a portion of the dissolved metal ions are removed from the onium hydroxide and/or salt solution; and collecting the onium hydroxide and/or salt solution after the contacting, wherein the solution collected contains a second quantity of dissolved metal ions smaller than the first quantity. The onium hydroxide and/or salt may be tetramethylammonium hydroxide and/or salt, and the metal content may be reduced to about 1 part per billion or less by the process.

Abstract: A carbonaceous material that has been loaded with at least one ionic organic species or hydroxide species and at least one metal or alkaline earth metal. The ionic organic species or hydroxide species is at least one selected from the group consisting of: fatty acids, surfactants, organic carboxyl species, organic sulfonate species, organic hydroxyl species, organic phenolic species, organic lactone species, organic amine species, or hydroxide species.

Abstract: An adsorptive bed having hydrous iron oxide and calcium carbonate materials. The adsorptive bed is useful in water treatment applications for removing metal contaminants, particularly for removing arsenic-containing ions.

Abstract: A method of purifying water in a nuclear installation includes an ion exchange mechanism in which the water is purified with an ion exchanger. Before being guided over the ion exchanger, the water is brought into contact with a catalyst in order to decompose hydrogen peroxide that is present in the water.

Abstract: Novel optionally hydrogenated nitrite rubbers distinguised by a very low ruthenium content are provided as well as a process for the removal of ruthenium-containing catalyst residues from a solution of optionally hydrogenated nitrite rubber by using specific functionalized ion-exchange resins.

Abstract: The present invention relates, generally, to the art of impregnating metal complexes into anion exchange materials to provide improved anion exchange materials with a metal inside the materials such that the modified materials effectively and efficiently remove or recover various metals, including metal containing complexes, compounds, and contaminants, such as arsenic, from, for example, process solutions, effluents and aqueous solutions. Uses for the improved anion exchange materials are also described as are methods of making modified anion exchange materials, and methods of removing and recovering at least one metal or contaminant from a source.

Abstract: In some embodiments, a system may reduce metal compounds from water. A system may include alginate particles in a housing. The alginate particles may be formed by directly adding alginate granules to an aqueous solution comprising metal ions, such as calcium ions.

Abstract: A system and method to remove a polluting agent or contaminant, including but not limited to mercury, from the liquid phase of a process system using an adsorbent. In one exemplary embodiment, a magnetic or non-magnetic support with a chemisorbing or physisorbing sorbent is suspended in the liquid phase of a process system, under conditions in which the polluting agent binds to the adsorbent. The pollutant-bearing adsorbent may then be separated from the process system by either physical or magnetic means. The polluting agent may then disassociated from the adsorbent so the adsorbent is regenerated and capable of repeated use.

Abstract: Chalcogenide compounds with cation exchange capability and methods of using the compounds are described. Compounds of the general formula A2xMxSn3-xS6 are described wherein x is 0.1-0.95, A is Li+, Na+, K+ or Rb+ and M is Mn2+, Mg2+, Zn2+, Fe2+, Co2+ or Ni2+. Compounds of the general formula H2xMxSn3-xS6 are also described wherein x is 0.1-0.95 and M=Mn2+, Mg2+, Zn2+, Fe2+, Co2+ or Ni2+. The compounds can be layered compounds. The compounds are capable of intercalation of Cs+, Sr2+, Hg2+, Pb2+, Cd2+, and/or Ag+ ions. A process involving contacting the compounds with a solution comprising one or more ions including Cs+, Sr2+, Hg2+, Pb2+, Cd2+, and/or Ag+ is also provided. The one or more ions can be removed from the solution by the compounds. A process comprising contacting compounds of the general formula A2xMxSn3-xS6 with a solution containing UO22+, Th4+ or Pu4+ ions is also described.

Abstract: A low-cost, water treatment system and method for reducing arsenic contamination in small community water storage tanks. Arsenic is removed by using a submersible pump, sitting at the bottom of the tank, which continuously recirculates (at a low flow rate) arsenic-contaminated water through an attached and enclosed filter bed containing arsenic-sorbing media. The pump and treatment column can be either placed inside the tank (In-Tank) by manually-lowering through an access hole, or attached to the outside of the tank (Out-of-Tank), for easy replacement of the sorption media.

Abstract: A method of manufacturing a remediation material is disclosed. The method includes providing a biogentic material as a substrate, preparing the surface of the substrate for a chemical reaction, and performing template-driven surface derivitization on the surface of the substrate to provide a net positive charge on the surface of the substrate. The remediation material may be placed into contact with surface water, ground water, soil, or sediment by at least one of a permeable reactive barrier, direct well injection, or direct introduction of the remediation material into soil or sediment, to remove contaminants from the surface water, ground water, soil, or sediment.

Abstract: Present invention deals with cost-effective surface-modified zeolite materials developed from commercial zeolites and flyash-based zeolites by treating with surface modifiers like hexadecyltrimethyl ammonium bromide (HDTMA-Br). The formation of zeolitic materials with anionic characteristics requires treatment with a surfactant with initial concentrations greater than its critical micelle concentration (CMC). The sorption of oxyanions on the surfactant-modified zeolite (SMZ) is attributed to surface complexation and surface precipitation. Incorporation of metal ions on SMZ showed improved anion uptake for dearsenification of water due to synergistic effects and is able to meet the stringent target of 10 ppb of As on potable water being adopted by most countries. High selectivity, faster kinetics and high adsorption capacity ensures cost effectiveness of this product as compared to other low-cost products for dearsenification.

Abstract: The present invention relates, generally, to the art of impregnating metal complexes into anion exchange materials to provide improved anion exchange materials with a metal inside the materials such that the modified materials effectively and efficiently remove or recover various metals, including metal containing complexes, compounds, and contaminants, such as arsenic, from, for example, process solutions, effluents and aqueous solutions. Uses for the improved anion exchange materials are also described as are methods of making modified anion exchange materials, and methods of removing and recovering at least one metal or contaminant from a source.

Abstract: Polyazacrown polymers based on the azacrown monomer 1,4,7,10,13,16,21,24-octaazabicyclo[8.8.8]hexacosane (“H6Aza222”) are disclosed. Azacrown monomer units are preferably linked with a suitable linking agent, and the resulting polymers are can absorb mercury from a water stream and form a stable complex therewith. Methods of making and using the polyazacrown polymers are also disclosed. The polymers have a high absorption capacity for and selectivity towards mercury, which properties are useful for the remediation of mercury-contaminated water. The polymers can be regenerated by the efficient removal of the absorbed mercury. Further, the absorbed mercury that is liberated from the polyazacrown polymers can be effectively concentrated and captured to prevent its re-release into the environment.

Abstract: A method for removing a metal from a metal-containing solution comprising contacting the metal-containing solution with a metal-removing composition comprising a substrate, an organic ion, and a metal binding agent, and recovering a solution having a lowered metal concentration when compared to the metal-containing solution.

Abstract: The invention relates to a combined process for the adsorption of metals in a liquid and for the neutralisation of metal-containing waste acids. The adsorption material used in the process is in the form of a geological mineral containing at least one alkali metal and/or alkaline earth metal, e.g. wollastonite (CaSiO3) , magnesite (MgCO3) or burnt magnesite (MgO). The spent adsorption material that has been used in the adsorption process is thereafter used as neutralisation agent for the neutralisation of waste acids, such as spent pickling baths. The application moreover relates to an adsorption material comprising a geological mineral containing at least one alkali metal and/or alkaline earth metal, which mineral has been concentrated by crushing, milling and shake sieving in a dry state.

Abstract: The current invention is concerned with methods and compositions for the removal of arsenic contamination from water. A method for binding As to oxidized metal coated pumice and method for making the same are disclosed. Water filters comprising oxidized metal coated pumice, such as oxidized iron coated pumice, are also provided.

Abstract: Wastewater streams from semiconductor processing operations are treated to reduce the concentration therein of one or more metal species to a satisfactory level. The disclosed systems and technique utilize complexing ion exchange media to treat the wastewater streams having a significant concentration of oxidizing species.

Abstract: A system for use in the removal of heavy metal contaminants from fluid is provided. The system includes a source from which contaminated fluid may be introduced into the system, a first station for removal by physical separation of a targeted heavy metal contaminant from the flow of fluid, including elemental species of the targeted heavy metal contaminant, and a second station positioned downstream of the first station and in fluid communication therewith for adsorptive separation of the targeted heavy metal contaminant from the fluid flow, including additional amount of the elemental species along with the other species of the targeted heavy metal contaminant. A method for removing heavy metal contaminants from fluid is also provided.

Abstract: Disclosed herein is a purification method characterized by adding a chitosan powder or a chitosan-coated substance, and optionally further adding a silica sol to liquor and filtering the mixture by a filter machine to remove unsaturated fatty acids, compounds of unsaturated fatty acids with metal ions, or fusel oil from the liquor.

Abstract: Method for removing Arsenic from water. The method includes providing resin based medium which contains Arsenate adsorbent agent and Arsenite oxidizing agent. The method also includes providing for water containing Arsenic to come in contact with the resin based medium. Corresponding composition for the Arsenic removal medium is also provided. Method for preparing the corresponding Arsenic removal medium is also provided.

Abstract: The present invention relates to a method for removing a heavy metal from and/or dissolving calcium and/or magnesium scales in water or an aqueous system comprising using ?-polyglutamic acid (?-PGA, H form), and/or one or more of its salts (i.e., ?-polyglutamate in Na+ form, ?-polyglutamate in K+ form, and ?-polyglutamate in NH4+ form) and/or ?-polyglutamate hydrogel as chelating agents for removing heavy metals and/or dissolving agents for removing calcium and/or magnesium scales from water or the aqueous system.

Abstract: The invention relates to the use of used alumina to reduce the level of inorganic contaminants, such as mercury and arsenic, from waste fluid streams. The invention further provides a process for reducing the level of mercury or arsenic in fluid streams by contacting the fluid stream with used alumina, such as used Claus catalyst.

Abstract: Systems and methods are provided for the removal and disposal of arsenic from an aqueous medium. The systems and methods include the removal of arsenic from a source by contact with either a chemically treated natural or synthetic zeolite, for example a ferric-loaded zeolite. The spent zeolite is disposed of at an appropriate arsenic disposal site. A system for monitoring and maintaining an arsenic removal/disposal system by an off-site provider is also disclosed.

Abstract: The use of a sulfur-impregnated organoclay provides a mercury or arsenic removal media having increased reactivity, stability, and mercury removal ability. The Hg/As removal media described herein is prepared by impregnating an organophilic clay with elemental (free state) sulfur. Alternatively, the clay can be made organophilic by onium ion reaction prior to or simultaneously with impregnating the organoclay with sulfur.

Abstract: The use of two mercury and arsenic removal media: A) a sulfur-impregnated organoclay; and B) a coupling agent-reacted organoclay, wherein the coupling agent preferably contains a mercapto, disulfide, tretrasulfide and/or polysulfide end group provides mercury removal media having increased reactivity, stability, and synergistic mercury removal ability. The preferred mercury removal media described herein is prepared by reacting an organophilic clay containing onium ions A) with elemental sulfur; and B) with a sulfur-containing coupling agent, preferably containing a mercapto, disulfide, tetrasulfide, and/or polysulfide moiety.

Abstract: The use of a sulfur-impregnated organoclay provides a mercury or arsenic removal media having increased reactivity, stability, and mercury removal ability. The Hg/As removal media described herein is prepared by impregnating an organophilic clay with elemental (free state) sulfur. Alternatively, the clay can be made organophilic by onium ion reaction prior to or simultaneously with impregnating the organoclay with sulfur.

Abstract: The use of a coupling agent containing a mercapto, disulfide, tretrasulfide and/or polysulfide end group provides a mercury removal media having increased reactivity, stability, and mercury removal ability. The mercury removal media described herein is prepared by reacting an organophilic clay containing onium ions with a mercapto, disulfide, tetrasulfide, and/or polysulfide end moiety. Alternatively, the clay can be made organophilic by onium ion reaction prior to or simultaneously with the coupling reaction of the mercapto- or sulfide- end group-containing coupling agent.

Abstract: The use of two mercury and arsenic removal media: A) a sulfur-impregnated organoclay; and B) a coupling agent-reacted organoclay, wherein the coupling agent preferably contains a mercapto, disulfide, tretrasulfide and/or polysulfide end group provides mercury removal media having increased reactivity, stability, and synergistic mercury removal ability. The preferred mercury removal media described herein is prepared by reacting an organophilic clay containing onium ions A) with elemental sulfur; and B) with a sulfur-containing coupling agent, preferably containing a mercapto, disulfide, tetrasulfide, and/or polysulfide moiety.

Abstract: The present invention relates to novel ion exchangers comprising carboxyl groups and also —(CH2)mNR1R2 groups having improved exchange kinetics and selectivity, a method for their production and also use thereof for the adsorption of metals, in particular arsenic, when these are additionally loaded with iron oxide/iron oxyhydroxide.

Abstract: A method for treating water to produce potable water is described herein. The inventive method enables the efficient removal of iron, manganese, and arsenic without the addition of powerful oxidants and without requiring a complex procedure for preparing the filtering material. The described method treats the water by passing the water through at least one bed of filter material, where the filter material comprises an association of manganese dioxide grains and at least one iron-based divided material in the hydroxide, oxide, or metallic state. The association may comprise a mixture of the iron-based divided material and the manganese dioxide grains. Alternatively, the association may comprise a superposition of layers of the iron-based divided material and the manganese dioxide grains.