Disclosed are a functional material for synchronously stabilizing multiple metals and a preparation method thereof, and a method for rehabilitating soil or wastewater contaminated by heavy metals (metalloids). The preparation method includes: mixing a ferrous salt, a ferric salt, a manganous salt, water, a dispersing material, and a phosphate to obtain a first mixture, and subjecting the first mixture to a first precipitation reaction to obtain a first reaction mixture containing the phosphate; adjusting a pH value of the first reaction mixture containing the phosphate to 10-12 by adding an alkali thereto to obtain a second mixture, subjecting the second mixture to a second precipitation reaction to obtain a second reaction mixture; and subjecting the second reaction mixture to a solid-liquid separation to obtain a solid, washing the solid, and drying to obtain the functional material for synchronously stabilizing multiple metals.

Compositions including a matrix, methods of making such compositions, structures including such compositions, methods of disposing such compositions on a substrate; wherein the matrix includes: a plurality of polytetrafluroethylene fibrils formed from PTFE resin and a plurality of active particles.

A family of highly charged crystalline microporous metallophosphate molecular sieves designated PST-19 has been synthesized. These high charge density metallophosphates are represented by the empirical formula of:

R.sup.p+.sub.rA.sup.+.sub.mM.sup.2+.sub.xE.sub.yPO.sub.z

where A is an alkali metal such as potassium, R is an organoammonium cation such as tetraethylammonium, M is a divalent metal such as zinc and E is a trivalent framework element such as aluminum or gallium. The PST-19 family of materials are among the first MeAPO-type molecular sieves to be stabilized by combinations of alkali and quaternary ammonium cations, enabling unique compositions. The PST-19 family of molecular sieves has the SBS topology and catalytic properties for carrying out various hydrocarbon conversion processes and separation properties for separating at least one component.

A methyl iodide adsorber, comprising a zeolite containing at least one iodide-adsorbing metal or a compound thereof, wherein the zeolite is a hydrophobic zeolite. Also, a use of the adsorber and a method for the adsorption of methyl iodide.

The present invention relates to a water treatment agent, a preparation method therefor, a water treatment apparatus using the same, and an in-situ groundwater treatment apparatus and, more specifically, to: a water treatment agent comprising a carbon nanotube support, and -manganese dioxide nanoparticles adsorbed on the carbon nanotube support and having a particle size of 1,000 nm or less; a preparation method therefor; a water treatment apparatus using the same; and an in-situ groundwater treatment apparatus.

To provide a porous silica which is capable of effectively eliminating odors of methyl mercaptan, hydrogen sulfide, nonenal and the like, said odors being difficult to be eliminated by a silica porous material that contains no metal. A porous silica containing particles that are provided with primary pores, wherein the particles contain a metal containing substance complex having a particle size of 1-100 nm. This porous silica has a specific surface area of 500 m.sup.2/g or more.

A family of highly charged crystalline microporous metallophosphate molecular sieves designated PST-19 has been synthesized. These high charge density metallophosphates are represented by the empirical formula of:
R.sup.p+.sub.rA.sup.+.sub.mM.sup.2+.sub.xE.sub.yPO.sub.z
where A is an alkali metal such as potassium, R is an organoammonium cation such as tetraethylammonium, M is a divalent metal such as zinc and E is a trivalent framework element such as aluminum or gallium. The PST-19 family of materials are among the first MeAPO-type molecular sieves to be stabilized by combinations of alkali and quaternary ammonium cations, enabling unique compositions. The PST-19 family of molecular sieves has the SBS topology and catalytic properties for carrying out various hydrocarbon conversion processes and separation properties for separating at least one component.

A magnetic magnesium-manganese layered double metal oxide composite and preparation and application. A soluble magnesium salt and a soluble manganese salt are dissolved in water to obtain a magnesium-manganese salt complex liquid; and a soluble carbonate and a soluble hydroxide are dissolved in water to obtain a carbonate-hydroxide complex liquid; a ferroferric oxide powder is added to the carbonate-hydroxide complex liquid, and then ethanol is added for ultrasonic dispersion to obtain a dispersion liquid; then the magnesium-manganese salt complex liquid is added for aging, centrifuging, washing, drying, grinding for sieving, and calcinating at 250-550? C. to obtain a magnetic magnesium-manganese layered double metal oxide composite. The composite of the present invention has relatively strong magnetism to Cd removal, and is featured by high adsorption efficiency, rapid adsorption rate and stability. Moreover, the composite can not only immobilize Cd efficiently, but also can be separated and recycled by magnet.

A method for preparing a sorbent composition includes the steps of: applying, from a solution or a slurry, a layer of a copper compound on the surface of a support material, and drying the coated support material, wherein the thickness of the copper compound layer on the dried support is in the range 1-200 m.
The precursor may be converted to a sorbent suitable for removing heavy metals from liquids or gases by applying one or more sulphur compounds to sulphide the copper compound and form CuS.

Coated iron oxide (10) nanocrystal structures, superparamagnetic 10 nanoparticles, methods for synthesizing coated 10 nanocrystal structures, and methods for synthesizing superparamagnetic 10 nanoparticles are described herein. A coated 10 nanocrystal structure may comprise an iron oxide core, a manganese ferrite shell layer surrounding the core, and a bilayer coating surrounding the shell layer. The bilayer coating may include an inner oleic acid layer surrounding the shell layer and an outer layer surrounding the inner oleic acid layer.