A method of selectively extracting lithium from a lithium sulfate aqueous solution, the method comprising: (i) mixing an aluminum-containing sorbent material into the lithium sulfate aqueous solution to form a precursor mixture, wherein the aluminum-containing sorbent material is an aluminum hydroxide, aluminum oxide, or combination thereof; and (ii) heating the precursor mixture to a temperature of 50-200° C. to result in selective formation of a solid lithium-aluminum complex and mother liquor; and wherein the method may further comprise: (iii) recovering isolated lithium salt from the solid lithium-aluminum complex by heating the solid lithium-aluminum complex in water or aqueous solution at a temperature of 50-100° C. to result in delithiation of the solid lithium-aluminum complex with transfer of the lithium salt from the solid lithium-aluminum complex to the water or aqueous solution, along with production of aluminum hydroxide solid.

A method of selectively extracting lithium from a lithium sulfate aqueous solution, the method comprising: (i) mixing an aluminum-containing sorbent material into the lithium sulfate aqueous solution to form a precursor mixture, wherein the aluminum-containing sorbent material is an aluminum hydroxide, aluminum oxide, or combination thereof; and (ii) heating the precursor mixture to a temperature of 50-200° C. to result in selective formation of a solid lithium-aluminum complex and mother liquor; and wherein the method may further comprise: (iii) recovering isolated lithium salt from the solid lithium-aluminum complex by heating the solid lithium-aluminum complex in water or aqueous solution at a temperature of 50-100° C. to result in delithiation of the solid lithium-aluminum complex with transfer of the lithium salt from the solid lithium-aluminum complex to the water or aqueous solution, along with production of aluminum hydroxide solid.

A coated substrate (2a, 2b) adapted for hydrocarbon adsorption having at least one surface, and a coating on the at least one surface, the coating comprising particulate carbon and a binder, wherein the particulate carbon has a BET surface area of at least about 1300 m.sup.2/g; and at least one of: (i) a butane affinity of greater than 60% at 5% butane; (ii) a butane affinity of greater than 35% at 0.5% butane; (iii) a micropore volume greater than about 0.2 ml/g and a mesopore volume greater than about 0.5 ml/g. A bleed emission scrubber (1) and an evaporative emission control canister system (30) comprising the coated substrate (2a, 2b) are provided. They can control evaporative hydrocarbon emissions and may provide low diurnal breathing loss (DBL) emissions even under a low purge condition.

This invention relates to treated geothermal brine compositions containing reduced concentrations of lithium, iron and silica compared to the untreated brines. Exemplary compositions contain concentration of lithium ranges from 0 to 200 mg/kg, concentration of silica ranges from 0 to 30 mg/kg, concentration of iron ranges from 0 to 300 mg/kg. Exemplary compositions also contain reduced concentrations of elements like arsenic, barium, and lead.

This invention relates to treated geothermal brine compositions containing reduced concentrations of lithium, iron and silica compared to the untreated brines. Exemplary compositions contain concentration of lithium ranges from 0 to 200 mg/kg, concentration of silica ranges from 0 to 30 mg/kg, concentration of iron ranges from 0 to 300 mg/kg. Exemplary compositions also contain reduced concentrations of elements like arsenic, barium, and lead.

The invention relates to a process for preparing core-shell particles comprising the steps of (i) providing a dispersion of primary magnetic particles having a mean diameter lower than 200 nm in a solvent; (ii) adding one or more (semi-)metal (oxyhydr)oxide(s) and/or one or more precursor(s) of a (semi-)metal (oxyhydr)oxide to said dispersion; (iii) optionally adding a hydrolysis agent for said one or more precursor(s); (iv) injecting the dispersion in a spray dryer; whereby a (semi-)metal (oxyhydr)oxide shell is formed on the magnetic particles during spray drying. The invention also relates to particles obtainable by said process, to a formulation of said particles in a solvent and to the use of said particles or said formulation for RNA or DNA extraction.

A filter medium for removal of contaminants from wastewater. The filter medium includes a walnut shell particle having a metal hydro(oxide) nanoparticle bonded to the surface of the nut shell particle. The filter medium is particularly useful for treating produced water and wastewater generated in steam-assisted gravity drainage (SAGD) in recovery of hydrocarbons from oil sands to remove total organic carbon and silica. Processes for preparing the filter medium and for treating wastewater using the filter medium are also provided.

A filter medium for removal of contaminants from wastewater. The filter medium includes a walnut shell particle having a metal hydro(oxide) nanoparticle bonded to the surface of the nut shell particle. The filter medium is particularly useful for treating produced water and wastewater generated in steam-assisted gravity drainage (SAGD) in recovery of hydrocarbons from oil sands to remove total organic carbon and silica. Processes for preparing the filter medium and for treating wastewater using the filter medium are also provided.

A composite comprising a hydroxyapatite and at least one additive which is present during hydroxyapatite synthesis. The additive may be embedded or incorporated into or coated onto the hydroxyapatite. The additive preferably increases the hydroxyapatite porosity, e.g., providing a higher pore volume and/or BET surface area than a hydroxyapatite material without additive. The additive preferably comprises an activated carbon, chitosan, hopcalite, clays, zeolites, sulfur, and/or a metal such as Al, Sn, Ti, Fe, Cu, Zn, Ni, Cu, Zr, La, Ce, in the form of metal, salt, oxide, oxyhydroxide, and/or hydroxide. The hydroxyapatite may be calcium-deficient. The composite is in the form of particles having a D50 of at least 20 μm, a BET surface area of at least 120 m.sup.2/g; and/or a total pore volume of at least 0.3 cm.sup.3/g. An adsorbent material comprising a composite or a blend of composite with a hydroxyapatite without additive, and its use for removal of contaminants such as Hg, Se, As, and/or B from an effluent.

An adsorption structure unit prevents water leakage from an adsorption structure and improves the durability of the adsorption structure and the durability of the adsorption structure unit. An adsorption structure has a filter portion having a plurality of flow paths divided by a plurality of partition walls and a plugged portion shutting a feed water inflow or outflow end of the plurality of flow paths, a water-impermeable outer tube accommodating the filter portion, and a seal material blocking a gap between the filter portion and the outer tube in at least one end portion of the filter portion. An adsorption structure unit has the adsorption structure, a housing supplying feed water from one end of the adsorption structure, and discharging the feed water from the other end, and a ring member disposed between end portions on both sides of the outer tube and an inner surface of the housing.