A water treatment system includes an adsorption column including granular activated carbon (GAC) that adsorbs contaminants from untreated water onto the GAC, thereby producing treated water, a first electrode disposed at a proximal side of the adsorption column, with a gap between the first electrode and the GAC, a second electrode disposed at a distal side of the adsorption column, a drain outlet in fluid communication with the adsorption column for draining water out of the adsorption column, a gas inlet in fluid communication with the adsorption column for injecting a displacement gas into the adsorption column, a high voltage power supply electrically connected to one of the first electrode and the second electrode for generating a plasma discharge within the GAC, thereby regenerating the GAC within the adsorption column, and a gas outlet in fluid communication with the adsorption column for venting waste gas produced by the plasma discharge.

The present invention relates to a method for treating industrial water containing organic matter, said method comprising: a step of physical separation producing wastes and an effluent; a step of adsorption of at least one part of said organic matter present in said effluent on at least one adsorbent resin chosen from the group comprising the non-ionic cross-linked resins and the microporous carbon resins; a step of reverse osmosis filtration downstream from said adsorption step.

A promoted activated carbon sorbent is described that is highly effective for the removal of mercury from flue gas streams. The sorbent comprises a new modified carbon form containing reactive forms of halogen and halides. Optional components may be added to increase reactivity and mercury capacity. These may be added directly with the sorbent, or to the flue gas to enhance sorbent performance and/or mercury capture. Mercury removal efficiencies obtained exceed conventional methods. The sorbent can be regenerated and reused. Sorbent treatment and preparation methods are also described. New methods for in-flight preparation, introduction, and control of the active sorbent into the mercury contaminated gas stream are described.

A method for separating N.sub.2 from a hydrocarbon gas mixture containing N.sub.2 comprising the steps of: i) providing a bed of adsorbent selective for N.sub.2; (ii) passing the hydrocarbon gas mixture through the bed of adsorbent to at least partially remove N.sub.2 from the gas mixture to produce: (a) N.sub.2-loaded adsorbent and (b) N.sub.2-depleted hydrocarbon gas mixture; iii) recovering the N.sub.2-depleted hydrocarbon gas mixture; iv) regenerating the N.sub.2-loaded adsorbent by at least partially removing N.sub.2 from the adsorbent; and v) sequentially repeating steps (ii) and (iii) using regenerated adsorbent from step (iv); wherein the adsorbent comprises a pyrolized sulfonated macroporous ion exchange resin.

The invention discloses a food container for preserving freshness of food, comprising a container body having a cavity adapted for containing food items; a lid detachably secured on the container body to close the cavity of the container; and one or more food preserving elements capable of absorbing food spoiling gas to preserve freshness of the food items. The one or more food preserving elements are disposed inside the cavity and/or into a material of the food container to preserve the food items for an extended period of time and remove odors.

A solid-liquid separation device performs dehydration or deoiling from a treated object using a substance A that is a gas at normal temperature and pressure and is capable of dissolving water and oil when liquefied. The separation device includes a substance B that circulates while generating phase change in a closed system, a compressor that compresses the substance B, a first heat exchanger that condenses substance B and evaporates of the substance A, an expansion valve that decompresses the condensed substance B, a second heat exchanger that evaporates substance B and condenses substance A, and a treatment tank wherein substance A is mixed with the treated object, substance A is evaporated while separated from the liquid in the first heat exchanger, and condensed in the second heat exchanger. The center of gravity of the first heat exchanger is lower than the second heat exchanger in a vertical direction.

A method and system for manufacturing and using a self-supporting structure in processing unit for adsorption or catalytic processes. The self-supporting structure has greater than 50% by weight of the active material in the self-supporting structure to provide a foam-geometry structure providing access to the active material. The self-supporting structures, which may be disposed in a processing unit, may be used in swing adsorption processes and other processes to enhance the recovery of hydrocarbons.

Mixed adsorbent/desiccant beds comprising in some embodiments from about 20 vol % (volume percent) to about 90 vol % of one or more adsorbents and from about 10 vol % to about 80 vol % of one or more desiccants, based on the total volume of the adsorbent/desiccant mixture, prevent water reflux during thermal regeneration of adsorption beds in gas processing plants and methods.

There are disclosed systems and processes that substantially prevent scaling in the treatment of a spent carbon material in a wet air oxidation (WAO) system.

A hydrogen gas recovery system according to the present ingestion is configured by a condensation and separation apparatus (A) that condenses and separates chlorosilanes from a hydrogen-containing reaction exhaust gas exhausted from a polycrystalline silicon production step, a compression apparatus (B) that compresses the hydrogen-containing reaction exhaust gas, an absorption apparatus (C) that absorbs and separates hydrogen chloride by contacting the hydrogen-containing reaction exhaust gas with an absorption liquid, a first adsorption apparatus (D) comprising an adsorption column filled with activated carbon for adsorbing and removing methane, hydrogen chloride, and part of the chlorosilanes each contained in the hydrogen-containing reaction exhaust gas, a second adsorption apparatus (E) comprising an adsorption column filled with synthetic zeolite that adsorbs and removes methane contained in the hydrogen-containing reaction exhaust gas, and a gas line (F) that recovers a purified hydrogen gas having a reduced concentration of methane.