A method of making copper sulfide electrode material comprising steps of: 1) stirring and dissolving copper(ii) nitrate hydrate (Cu(NO.sub.3)2.3H.sub.2O) and Thiourea (CH.sub.4N.sub.2S) in a mixed solution consisting of ethylene glycol and deionized water; 2) adding hexadecyl trimethyl ammonium bromide (C.sub.19H.sub.42N.Br) to mixture A; 3) placing the mixture B into a roaster, raising a temperature of the roaster to 100° C. to 180° C. for 10 hours to 18 hours; 4) washing the crude CuS by using a mixed fluid of ethanol absolute (C.sub.2H.sub.6O) and deionized water to be cooled in a room temperature, placing the crude CuS in the roaster and raising a temperature of the roaster to 50° C. to 80° C.; 5) producing cathode electrode of asymmetric capacitive deionization module by using the copper sulfide electrode material; 6) producing anode electrode of asymmetric capacitive deionization module by using activated carbon electrode material.

Provided herein are processes for the removal and/or recovery of a target metal from a liquid sample, said process comprising: [1] applying acoustic cavitation to the liquid; and [2] adding an iron (II) salt, or a precursor form thereof, to the liquid sample and allowing Fenton oxidation reaction to occur between the iron and hydrogen peroxide in the liquid, thereby producing hydroxyl radicals; thereby producing a target metal salt or metal oxide having a reduced solubility in the liquid sample, leading to removal of the target metal from the liquid sample. The use of metal ligands in such processes is also described, as well as systems for performing such processes. Methods, processes, and systems for removing organic contaminants from a liquid sample are also described.

An atomizer for use in a water treatment system includes an influent inlet, to receive a flow of fluid containing contaminants a gas flow inlet, to receive a flow of gas to be mixed with the fluid in a mixing zone, an airflow controlling component, including an array of vanes disposed between the gas flow inlet and the mixing zone to impart a rotational component to a direction of flow of the gas. A channel receives the flow of fluid containing contaminants, and conducts the flow of fluid containing contaminants to the mixing zone, wherein radially outwardly flowing fluid containing contaminants is mixed with radially inwardly flowing gas to atomize the fluid containing contaminants, and an outlet.

A device for decomplexation and enhanced removal of copper based on self-induced Fenton-like reaction constructed by electrochemistry coupled with membrane separation is disclosed. The device includes a reactor, two electrocatalytic anodes capable of generating hydroxyl radicals, an electrocatalytic cathode membrane assembly, a direct current power supply, an aeration system, an inlet pipe and an outlet pipe. The device of the present invention has a simple construction. Using this device to treat industrial wastewater containing copper complexes under specific conditions allows the decomplexation and the removal of the industrial wastewater containing the copper complexes to be simultaneously realized at a low consumption and a high efficiency. The coupling of electrochemistry with membrane separation can be achieved to protect the cathode from being contaminated by pollutants in the sewage and prolong the service life of the electrode.

Compounds are described which include polyvalent ligands linked to a cyclodextrin scaffold which exhibit strong binding affinities for lanthanides and favorable characteristics with respect to altering the relaxation time of coordinated water molecules. The compounds are useful as contrast agents in applications such as magnetic resonance imaging. The polyvalent ligands are also useful in applications requiring chelation of metal ions in other applications such as water treatment, sequestration of metal ions and treatment of diseases or conditions caused by exposure to toxic or radioactive metal ions.

Crosslinked polymers made up of polymerized units of cyclic diaminoalkane, aldehyde and bisphenol-S or melamine. A method for removing heavy metals, such as Pb(II) from an aqueous solution or an industrial wastewater sample with these crosslinked polymers is introduced. A process of synthesizing the crosslinked polymers is also described.

Disclosed is a filter for a water-purification device, the filter including a filter housing having a water inlet and a water outlet defined therein; and a filter member disposed in the filter housing to purify water introduced through the inlet and supply the purified water to the outlet, wherein the filter member includes a carbon block produced by mixing 40 to 50% by weight of titanium oxide, 30 to 40% by weight of activated carbon, and 18 to 23% by weight of binder with each other. Further, a water-purification device including the filter is disclosed.

Crosslinked polymers made up of polymerized units of cyclic diaminoalkane, aldehyde and bisphenol-S or melamine. A method for removing heavy metals, such as Pb(II) from an aqueous solution or an industrial wastewater sample with these crosslinked polymers is introduced. A process of synthesizing the crosslinked polymers is also described.

Described are filter materials having polycarboxyl ligands, such as iminodiacetic acid, which are highly effective for filtering metals or metal ions from fluids. The filter materials can be particularly useful to filter various fluid compositions, such as those used for wet etching, removing photoresist, and cleaning steps in microelectronic device manufacturing.

The present invention relates to a method for treating an aqueous liquid effluent containing calcium and carbonate ions and containing precipitation-inhibiting products, said process comprising the following successive steps: a) providing an aqueous liquid effluent supersaturated with CaCO.sub.3 and containing precipitation-inhibiting products; b) having the effluent obtained in step a) pass into a reactor with high solid content with a solid content maintained between 20 and 800 g/l and integrated solid-liquid separation, at a pH comprised between 8 and 9.2 allowing in a single step precipitation in situ of the aragonite polymorph of calcium carbonate and removal of the precipitation-inhibiting products; c) recovering an aqueous liquid supernatant containing a suspended solids content of less than or equal to 0.1% by mass of the solid content in the reactor, advantageously a suspended solids content of less than 50 mg/l, the precipitation-inhibiting products being phosphonates.