Systems and methods for use in extracting oil from solid plant-based materials are described. The systems and methods use an electrolyzed carrier fluid made from a hydroxide brine for contacting with plant-based material to thereby separate oil from solid plant particulate. The electrolyzed carrier fluid can have a reductive oxidation-reduction-potential (ORP) of −700 mV or more, such as in the range of from about −900 mV to about −1000 mV.

A gas dissolved liquid manufacturing device includes: a pump configured to pressurize a liquid; a pipe communicating with the pump; a nozzle disposed in the pipe, the nozzle being configured to generate micro bubbles using a supplied gas; and a gas-liquid separation tank whose upper part communicates with the pipe, the gas-liquid separation tank being configured to separate a gas-liquid mixture generated by the nozzle into a gas and a liquid.

A gas dissolved liquid manufacturing device includes: a pump configured to pressurize a liquid; a pipe communicating with the pump; a nozzle disposed in the pipe, the nozzle being configured to generate micro bubbles using a supplied gas; and a gas-liquid separation tank whose upper part communicates with the pipe, the gas-liquid separation tank being configured to separate a gas-liquid mixture generated by the nozzle into a gas and a liquid.

A method and system for reversibly converting water between an initial ionic strength and an increased ionic strength, using a switchable additive, is described. The disclosed method and system can be used, for example, in distillation-free removal of water from solvents, solutes, or solutions. Following extraction of a solute from a medium by dissolving it in water, the solute can then be isolated from the aqueous solution or “salted-out” by converting the water to a solution having an increased ionic strength. The solute then separates from the increased ionic strength solution as a separate phase. Once the solute is, for example, decanted off, the increased ionic strength aqueous solution can be converted back to water having its original ionic strength and reused. Switching from lower to higher ionic strength is readily achieved using low energy methods such as bubbling with CO.sub.2, CS.sub.2 or COS. Switching from higher to lower ionic strength is readily achieved using low energy methods such as bubbling with air, heating, agitating, introducing a vacuum or partial vacuum, or any combination or thereof.

A sequential batch reactor wastewater treatment system and method, a material combination for practicing the method, and a fertilizer co-product deriving therefrom. A pH lowering agent comprising an acid lowers the pH of wastewater. A first compound including chitin or chitosan comprises a filtering medium, a coagulant, and a flocculant, and a second compound comprises an adsorbent and a pH raising agent. Wastewater is mixed and aerated subsequent to introduction of each of the first and second compounds, and flocculation yields treated water and a sludge byproduct that may be dewatered and further processed to yield a useful fertilizer co-product. Within the first compound, diatomaceous earth operates as a filtering medium and bentonite clay acts as a coagulant and filtering medium. Within the second compound, activated carbon, calcium oxide (CaO), and caustic soda (NaOH) are operative to adsorb, disinfect, and raise the pH of the wastewater.

The water outlet of a subsystem that includes an ultraviolet oxidation device and the water inlet of each substrate treatment device are connected to each other via a main pipe. A hydrogen peroxide removal device is installed between the ultraviolet oxidation device of the subsystem and a non-regenerative ion-exchange device. In addition, a carbon dioxide supply device is installed at the middle of a pipe that branches from the water outlet of the subsystem to reach the substrate treatment device. According to an aspect, the hydrogen peroxide removal device is filled with a platinum-group metal catalyst. Thus, ultrapure water passed through the ultraviolet oxidation device is used as a base to produce carbonated water in which the concentration of hydrogen peroxide dissolved therein is limited to 2 μg/L or less and to which carbon dioxide is added to adjust resistivity to be within the range of 0.03 to 5.0 MΩ.Math.cm.

The water outlet of a subsystem that includes an ultraviolet oxidation device and the water inlet of each substrate treatment device are connected to each other via a main pipe. A hydrogen peroxide removal device is installed between the ultraviolet oxidation device of the subsystem and a non-regenerative ion-exchange device. In addition, a carbon dioxide supply device is installed at the middle of a pipe that branches from the water outlet of the subsystem to reach the substrate treatment device. According to an aspect, the hydrogen peroxide removal device is filled with a platinum-group metal catalyst. Thus, ultrapure water passed through the ultraviolet oxidation device is used as a base to produce carbonated water in which the concentration of hydrogen peroxide dissolved therein is limited to 2 μg/L or less and to which carbon dioxide is added to adjust resistivity to be within the range of 0.03 to 5.0 MΩ.Math.cm.

A system and method for removing ammonia from an ammonia-containing liquid is described. The system comprises a primary heat exchanger 12 for heating the ammonia-containing liquid to operational temperature, an ammonia stripper 14 for stripping ammonia from the ammonia-containing liquid from the primary heat exchanger and discharging it as ammonia-containing gas, and an acid scrubber 16 for reacting the ammonia in the ammonia-containing gas with acid to form an ammonium salt. The acid scrubber comprises a scrubbed air outlet 32 in fluid communication with a hot air inlet 20 of the ammonia stripper, such that scrubbed air which is discharged from the acid scrubber may be recycled for use in the ammonia stripper. Also described is a system and method for removing ammonia from an ammonia-containing liquid, wherein the system comprises a cold-water scrubber for removing ammonia from the ammonia-containing gas discharged from the ammonia stripper.

A system and method for removing ammonia from an ammonia-containing liquid is described. The system comprises a primary heat exchanger 12 for heating the ammonia-containing liquid to operational temperature, an ammonia stripper 14 for stripping ammonia from the ammonia-containing liquid from the primary heat exchanger and discharging it as ammonia-containing gas, and an acid scrubber 16 for reacting the ammonia in the ammonia-containing gas with acid to form an ammonium salt. The acid scrubber comprises a scrubbed air outlet 32 in fluid communication with a hot air inlet 20 of the ammonia stripper, such that scrubbed air which is discharged from the acid scrubber may be recycled for use in the ammonia stripper. Also described is a system and method for removing ammonia from an ammonia-containing liquid, wherein the system comprises a cold-water scrubber for removing ammonia from the ammonia-containing gas discharged from the ammonia stripper.

A filtration apparatus includes a tubular casing having a longitudinal axis and first and second casing ends, a plurality of partition plates positioned in the casing and sealed thereto to thereby define a plurality of axially successive chambers within the casing, including an intake collection chamber between a first of the partition plates and the first casing end, a discharge collection chamber between a second of the partition plates and the second casing end, and a reject collection chamber opposite the second partition plate from the second casing end. A plurality of elongated filtration membrane stacks are positioned side-by-side in the casing generally parallel to the longitudinal axis. Each filtration membrane stack includes an intake end which is fluidly connected to the intake collection chamber, a discharge end which is fluidly connected to the reject collection chamber, and a permeate channel which extends between the intake and discharge ends and is fluidly connected to the discharge collection chamber, an end of the permeate channel located adjacent the intake end being sealed from the intake collection chamber. The filtration apparatus also includes an intake pipe having a first end fluidly connected to the intake collection chamber and a second end fluidly connected to a first connector located proximate the second casing end; a discharge pipe having a first end fluidly connected to the discharge collection chamber and a second end fluidly connected to a second connector located proximate the first connector; and a reject pipe having a first end fluidly connected to the reject collection chamber and a second end fluidly connected to a third connector located proximate the first and second connectors. Each filtration membrane stack includes a plurality of filtration membranes, and the plurality of filtration membrane stacks together define a plurality of axially successive sets of radially adjacent filtration membranes. Also, each filtration membrane of each of the sets of filtration membranes is sealed to a corresponding hole in a respective one of the partition plates.