A wastewater management system includes a series of water treatment modules to treat wastewater and produce reusable and/or potable water and other beneficial byproducts of the wastewater treatment process. A pretreatment module, a filtration module, an evaporator module, an odor control module, a UV-light module, an autoclave module, a sonolysis module, an ozone module and a chlorination module are combined in multiple combinations along with holding tanks, condensers, flash tanks and other components to address water purification and reclamation needs based upon specific wastewater conditions. The system captures condensate from AC systems and rainwater from rainwater gutter systems processes the water to produce reusable and/or potable water with or without re-mineralization. Any CO.sub.2 produced by the water treatment system is captured and processed using naturally-occurring flora. The wastewater treatment system includes multiple closed-loop subsystems to minimize energy usage and maximize water purification and reclamation for reuse.

The present disclosure relates to a solid and hydrolyzable tablet for treating contaminated water. The tablet comprises at least one an active ingredient chosen from a precipitating agent, alone or in combination with an agglomerating agent. The disclosure also relates to the use of a tablet for treating contaminated water. The disclosure also relates to a method and a device for treating contaminated water. The method comprises placing water laden with contaminant in contact with a precipitating agent and/or an agglomerating agent, dissolving these agents, mixing these dissolved agents with the water laden with contaminant so as to precipitate and/or agglomerate the contaminant, then separating said contaminant so as to obtain treated water.

Reactive treatment cells (RTCs) are described in combination with sediment capping systems as a means for environmental remediation. RTCs include an impermeable housing defining an interior, a permeable ceiling and floor typically including filtration materials such as geotextiles, and at least one interior compartment for treatment reagents. One RTC includes a gabion-like cage structure retaining a geomembrane-supported geosynthetic clay liner (GM-GCL) housing, while a second embodiment includes a hard, cylindrical shell as a replaceable reagent cartridge. RTCs may be employed in initial capping system installations or retrofitted into existing capping systems. RTCs may include optional baffles, flow restrictors, floating discs, sensor probes, and two or more serial reagent zones or compartments.

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.

An iron-carbon composite material and a preparation method thereof are disclosed. The iron-carbon composite material includes a three-layer core-shell structure, which successively includes a porous graphite carbon outer layer, an iron carbide intermediate layer and a nano zero-valent iron core from outside to inside. The present invention wraps nano zero-valent iron in porous graphite carbon and iron carbide, which can prevent the oxidation of nano zero-valent iron, while iron carbide effectively improves the ability to fix arsenic, realizing high efficiency and long-term use of nano zero-valent iron. Iron carbide may effectively adsorb and fix arsenic, and especially efficiently oxidize As(III) to relatively low-toxic As(V).

The present invention is directed to an electrochemical device for at least partially removing or reducing a target ionic species from an aqueous solution using faradaic immobilization, the electrochemical device including at least one first electrode and at least one second electrode with different void fraction and surface area properties, due to differences in void fraction (also referred to as void ratio) of the at least one first and the at least one second electrode, water flows through an electrode with a high porosity, while the aqueous solution does not flow through an electrode with a low porosity. The asymmetry of the electrodes provides a desired voltage distribution across the device, which equates to a different voltage at each electrode, to control the speciation of the target ionic species at the anode and the cathode.

Measurement devices can be used for identifying concentration of arsenic species in water samples. The measurement devices can take the form of test strips including a substrate with at least one testing region that includes an amount of a testing medium. The silver reagent includes a polymer framework and a silver component that is stabilized by the framework, yet remains reactive enough to function as a colorimetric sensor for arsenic, e.g., ((Ag(H.sub.2btc))(Ag.sub.2(Hbtc))).sub.n. The initially substantially colorless testing medium exhibits a color change response when exposed to arsenic species, e.g., arsine, generated from samples including as little as 5 ppb arsenic, with an increasingly dark color as the concentration of arsenic is increased. Test strips fabricated with the silver coordination polymer display robust stability towards both light and water, allowing for an alternative to mercury-based field test kits in real-world field tests under direct sunlight and high humidity conditions.

An adsorbent for a target compound can include porous carbon particles having pores with a predominant pore size less than 10 nm, and magnetic nanoparticles (MNP) nucleated on the carbon surface and within the pores of carbon particles to provide a carbon magnetic nanoparticle adsorbent (C-MNA). A method for removing target compounds with an adsorbent, a system for removing contaminants from a liquid, and a method for adsorbing target compounds from a fluid are also disclosed.

This invention relates to a process for treating acid mine drainage (AMD). The process includes the steps of adjusting the pH of the AMD to be in the range of 3 to 5; adding maghemite nanoparticles to form a slurry; and a) aerating the slurry obtained in step 3), or b) simultaneously heating and mixing the slurry obtained in step 3). Thereafter maghemite nanoparticles loaded with one or more metals and sulphate and precipitated metals is separated from the slurry.

A filter includes a porous molded article, which is a sintered material of mixed powder containing activated carbon powder and thermoplastic resin powder. When water having a specific electrical resistance value of 18 MΩ.Math.cm or greater is caused to pass through the filter at a space velocity of 1200 hr.sup.−1, a specific electrical resistance value of the water after being caused to pass through the filter is 13 MΩ.Math.cm or greater. To provide a filter capable of efficiently removing metal ions in a treatment liquid and capable of easily obtaining a solution having an extremely low metal ion content.