A method including reacting, at a jobsite, a total dissolved solids (TDS) water with a gas comprising carbon dioxide (CO.sub.2) in the presence of a proton-removing agent to produce a CO.sub.2-reduced gas and an aqueous product comprising water and a precipitate, wherein the TDS water comprises produced water, wherein the precipitate comprises one or more carbonates, and wherein the CO.sub.2-reduced gas comprises less CO.sub.2 than the gas comprising CO.sub.2; and separating at least a portion of the water from the aqueous product to provide a concentrated slurry of the precipitate and a TDS-reduced water, wherein the TDS-reduced water comprises less TDS than the TDS water.

Novel methods for pretreating a rare-gas-containing stream exiting an etch chamber followed by recovering the rare gas from the pre-treated, rare-gas containing stream are disclosed. More particularly, the invention relates to the pretreatment and recovery of a rare gas, such as xenon or krypton, from a nitrogen-based exhaust stream with specific gaseous impurities generated during an etch process that is performed as part of a semiconductor fabrication process.

Techniques according to the present disclosure include capturing carbon dioxide from a dilute gas source with a CO.sub.2 capture solution to form a carbonate-rich capture solution; separating at least a portion of carbonate from the carbonate-rich capture solution; forming an electrodialysis (ED) feed solution; flowing a water stream and the ED feed solution to a bipolar membrane electrodialysis (BPMED) unit; applying an electric potential to the BPMED unit to form at least two ED product streams including a first ED product stream including a hydroxide; and flowing the first ED product stream to use in the capturing the carbon dioxide from the dilute gas source with the CO.sub.2 capture solution.

A method for capturing carbon from a source of volatile pollutants includes the steps of capturing a mixture of volatile pollutants and air from the source of volatile pollutants, transporting the volatile pollutant-air mixture to an oxidizer module, converting the volatile pollutants into carbon dioxide within the oxidizer module, transporting the carbon dioxide from the oxidizer module to a contactor, loading the carbon dioxide onto sorbents within the contactor, and separating the carbon dioxide from the loaded sorbents to produce a concentrated carbon dioxide product stream. The step of separating the carbon dioxide from the loaded sorbents may optionally include the steps of passing the loaded sorbents to the oxidizer module, and then heating the loaded sorbents in the oxidizer module with the combustion of the mixture of volatile pollutants and air within the oxidizer module to produce the concentrated carbon dioxide product stream while regenerating the sorbents.

Process and apparatus (10) are disclosed for capturing and converting an ozone-depleting alkyl halide fumigant from a fumigant/air mixed stream (14) by absorbing it into a metal hydroxide-alcohol buffer solution (26) in an absorber/scrubber (12) to produce a fumigant-free air stream (28). The captured alkyl halide in aqueous alcohol solution can actively react with the metal hydroxide in alcohol solution to produce a value-added product, such as a precipitate metal halide, and another alcohol that further enhances absorption. The absorbing solution is well-mixed with make-up alcohol and alkali streams to maintain the concentration of the metal hydroxide in the desired buffer solution range. The solid precipitate metal halide (52) is separated from the liquid stream, and the metal hydroxide-containing mixed alcohol stream (26) is recycled to the absorber/scrubber (12).

An entirely water-based, energy self-sufficient, integrated in-line waste management system is provided for comprehensive conversion of all organic fractions of municipal and wider community waste to fuels suitable for use in transportation, with all solid residues converted to high nutrition compost. The system is based on a combination of pre-treatment, involving alkaline hydrolysis and saponification; three-way separation of the pre-treated waste into different streams that are each directed to suitable further processing including fuel production; which includes biodiesel generation in a continuous-flow catalytic esterification unit, and anaerobic digestion to produce methane or other small molecule biofuel. Remaining solids are converted to compost in a quasi-continuous process.

An apparatus includes a housing that defines a first zone, a second zone, a third zone, and a fourth zone. The apparatus includes an inlet, a first outlet, a second outlet, and a conveyor belt. The inlet is configured to receive a carbon dioxide-containing fluid in the first zone. The first outlet is configured to discharge a carbon dioxide-depleted fluid from the first zone. The second outlet is configured to discharge a carbon dioxide-rich fluid from the third zone. The conveyor belt passes through each of the zones. The conveyor belt includes a carbon dioxide sorbent. Within the first zone, the carbon dioxide sorbent is configured to adsorb carbon dioxide from the carbon dioxide-containing fluid to produce the carbon dioxide-depleted fluid. Within the third zone, the carbon dioxide sorbent is configured to desorb the captured carbon dioxide to produce the carbon dioxide-rich fluid.

An organic iodine remover is a remover for removing organic iodine and is a substance composed of a cation and an anion, and the cation (for example, a phosphonium cation, an ammonium cation, or a sulfonium cation) has a molecular structure in which an electron donating group (for example, a phosphino group, an amino group, a sulfanyl group, a hydroxy group, or an alkoxy group) is bonded to a phosphorus atom, a nitrogen atom or a sulfur atom. An organic iodine removing apparatus includes: a vessel into which the organic iodine remover for removing the organic iodine is charged; and introduction pipes through which a fluid containing organic iodine is introduced into the organic iodine remover.

A treatment process for remediating H.sub.2S and other contaminants in liquids includes: partially filling a closed vessel with a contaminated liquid containing ≥5 ppm H.sub.2S with a head space above the liquid within the vessel where gasses released from the liquid from the liquid collect; separately providing a treatment composition in the head space so that the gasses from the liquid may contact the treatment composition; and permitting the contact between the vapors from the liquid and the treatment composition to continue until a collective concentration of H.sub.2S in the liquid and in the head space is <5 ppm. The treatment composition includes an aqueous solution containing at least one hydroxide compound, a collective concentration of the at least one hydroxide compound in the aqueous solution is in a range of 35-55 weight %, and the aqueous solution constitutes at least 80 weight % of the treatment composition.

A fossil fuel fired power plant exhaust gas clean-up and recovery system is provided to remove detrimental exhaust gases from the power plant exhaust and to produce and reclaim various commercial byproducts. A process includes mixing one liquid solution with a solubilizer in a mixing tank containing water to create a chemical reaction therein to produce an ionic solid compound and an alkaline liquid solution. Simultaneously directing the flue gases and the alkaline liquid solution into the wet scrubber to create a chemical reaction therein. The chemical reaction removes various detrimental exhaust gases from the flue gases and captures CO.sub.2 gases therefrom, which are chemically transferred into a newly formed sodium bicarbonate solution. The sodium bicarbonate solution exiting the wet scrubber is stored for resale or reuse in the subject process. The process uses various pathways to distribute the sodium bicarbonate for producing other byproducts.