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.

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.

Embodiments of the present disclosure are directed to systems and methods of removing carbon dioxide from a gaseous stream using magnesium hydroxide and then regenerating the magnesium hydroxide. In some embodiments, the systems and methods can further comprise using the waste heat from one or more gas streams to provide some or all of the heat needed to drive the reactions. In some embodiments, magnesium chloride is primarily in the form of magnesium chloride dihydrate and is fed to a decomposition reactor to generate magnesium hydrochloride, which is in turn fed to a second decomposition reactor to generate magnesium hydroxide.

A method for conversion of magnesium chloride into magnesium oxide and HCl includes the steps of providing a magnesium chloride compound to a thermohydrolysis reactor, the reactor being at a temperature of at least 300 C., withdrawing MgO from the thermohydrolysis reactor in solid form, and withdrawing an HCl containing gas stream from the thermohydrolysis reactor. The magnesium chloride compound provided to the thermohydrolysis reactor may be a solid magnesium chloride compound which comprises at least 60 wt. % of MgCl.sub.2.4H.sub.2O.

A method of treating a metal carbonate salt includes hydrolyzing a metal halide salt to form a hydrohalic acid and a hydroxide salt of the metal in the metal halide salt. The metal includes an alkaline earth metal or an alkali metal. The method includes reacting the hydrohalic acid with the metal carbonate salt, wherein the metal carbonate salt is a carbonate salt of the alkaline earth metal or alkali metal, to form CO.sub.2 and the metal halide salt. At least some of the metal halide salt formed from the reacting of the hydrohalic acid with the metal carbonate salt is recycled as at least some of the metal halide salt in the hydrolyzing of the metal halide salt to form the hydrohalic acid and the hydroxide salt.

Magnesium chloride solutions including providing aqueous magnesium chloride solution with magnesium chloride concentration of 10-30 wt. % to concentration step where water is evaporated, resulting in concentrated magnesium chloride solution with magnesium chloride concentration of 30-50 wt. %, wherein concentration step is carried out in one or more stages, wherein at least one of the stages is conducted at elevated pressure, withdrawing concentrated magnesium chloride solution from concentration step, and providing it to thermohydrolysis reactor of at least 300 C., withdrawing MgO from thermohydrolysis reactor in solid form, and withdrawing a HCl containing gas stream of at least 300 C. from thermohydrolysis reactor, providing the HCl-containing gas stream of at least 300 C. to cooling step, where HCl-containing gas stream is contacted with cooling liquid, withdrawing HCl-containing gas stream below 150 C. from cooling step, circulating cooling liquid through heat exchanger where energy is transferred to heating liquid which circulates from heat exchanger to concentration step.

A method includes treating a first brine stream including a plurality of minerals with an anti-scalant to produce a treated brine. The first brine stream is provided by a wastewater treatment system. The method also includes directing the treated brine to a first nanofiltration (NF) system disposed downstream from and fluidly coupled to the wastewater treatment system, generating a first NF permeate stream and a first NF non-permeate stream from the treated brine in the first NF system, directing the first NF non-permeate stream to a mineral removal system disposed downstream from and fluidly coupled to the first NF system, and removing the plurality of minerals from the first NF non-permeate stream to generate a first overflow stream in the mineral removal system. The first overflow stream comprises at least a portion of the plurality of minerals. The method also includes routing a first portion of the first overflow stream to a hydrochloric acid (HCl) and sodium hydroxide (NaOH) production system disposed downstream from and fluidly coupled to the mineral removal system. The HCl and NaOH production system includes a second NF system that may receive the first portion of the first overflow stream and may generate a second brine stream from the first portion of the first overflow stream. The method further includes directing the second brine stream to a first electrodialysis (ED) system disposed within the HCl and NaOH production system and fluidly coupled to the second NF system. The first ED system may generate HCl and NaOH from the second brine stream.

The present invention relates to an electrochemical process for generating or recovering hydrochloric acid from metal salt solutions such as acidic metal salt solutions and saline solutions. The process is useful for treating acidic salt solutions that are waste products from mineral processing or other industrial processes such as metal finishing, water softening, water treatment, reverse osmosis, electrodialysis, coal seam gas extraction, shale gas extraction and shale oil extraction, to generate high purity hydrochloric acid, metal salts and recycled water that may be re-used in the industrial process. An apparatus for performing the electrochemical process is also described.

The present invention relates to an electrochemical process for generating or recovering hydrochloric acid from metal salt solutions such as acidic metal salt solutions and saline solutions. The process is useful for treating acidic salt solutions that are waste products from mineral processing or other industrial processes such as metal finishing, water softening, water treatment, reverse osmosis, electrodialysis, coal seam gas extraction, shale gas extraction and shale oil extraction, to generate high purity hydrochloric acid, metal salts and recycled water that may be re-used in the industrial process. An apparatus for performing the electrochemical process is also described.

A process for the amelioration of acid mine drainage useful in shale hydrolyic fracturing operations for the production of natural gas involving the exchange of sulfate and chloride ions by an ion exchange resin so as to produce hydrochloric acid and water for use in hydrolyic fracturing operations from acid mine drainage.