A filter medium of the present invention includes a porous carbon material having a value of a specific surface area by a nitrogen BET method of 1×10.sup.2 m.sup.2/g or more, a volume of fine pores by a BJH method of 0.3 cm.sup.3/g or more, and a particle size of 75 μm or more, alternatively, a porous carbon material having a value of a specific surface area by a nitrogen BET method of 1×10.sup.2 m.sup.2/g or more, a total of volumes of fine pores having a diameter of from 1×10.sup.−9 m to 5×10.sup.−7 m, obtained by a non-localized density functional theory method, of 1.0 cm.sup.3/g or more, and a particle size of 75 μm or more.

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.

A process to treat metal or mineral ores is disclosed. The metal or mineral ore is a metallic sulphide ore including copper, gold, platinum, silver, nickel, molybdenum, arsenic sulphides, cobalt, zinc, lead, tin, antimony, or combinations thereof with a collector composition including a dimeric fatty nitrile. The dimeric fatty nitrile is prepared by a process including reacting a dimer fatty acid with ammonia at a temperature between about 200° C. and about 400° C. to form a dimeric amide and removing water from the dimeric amide to form the dimeric nitrile. The present disclosure also provides a collector composition containing the dimeric fatty nitrile and at least one further collector or frother compound.

A water treatment system filters out solid material containing carbon, and provides that solid material to a fermenter. Volatile fatty acids are produced within the fermenter. After fermentation, a second filtering operation is utilized to permit passage of water and volatile fatty acids while filtering out solids from the fermenter. The volatile fatty acids are used as a food source for bacteria during secondary treatment of the water.

In one aspect, separation media are described herein operable for removing one or more water contaminants including NOM and derivatives thereof. Briefly, a separation medium includes a nanoparticle support and an oligomeric stationary phase forming a film on individual nanoparticles of the support, the film having thickness of 1 to 100 nm. In some embodiments, oligomeric chains of the stationary phase are covalently bonded to the individual nanoparticles.

Processes for producing olefins may include electrolyzing an aqueous solution comprising metal chloride, where electrolyzing the aqueous solution causes at least a portion of the metal chloride to undergo chemical reaction to produce a treatment composition comprising hypochlorite. The processes may further include contacting at least a portion of the treatment composition with the sour water at a pH from 8 to 12, where the sour water comprises sulfides and the contacting causes reaction of the sulfides in the sour water with the hypochlorite to produce a treated aqueous mixture comprising at least metal sulfates and metal chlorides, where the metal sulfates are present in the treated aqueous mixture as precipitated solids. The processes may further include separating the precipitated solids from the treated aqueous mixture to produce a treated effluent comprising at least the metal chloride.

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 multifunctional additive including a biochelant and a sulfide scavenger. A method of servicing a cooling tower including contacting an industrial water present in the cooling tower with an additive comprising a biochelant and a sulfide scavenger. A method of servicing a wellbore including contacting an industrial water produced from the wellbore with an additive including a biochelant and a sulfide scavenger.