Described herein are salt-splitting electrolysis systems, which comprise flow electrodes, and methods of operating such systems. Specifically, the flow electrodes comprise active particles (suspended in a solvent) with catalysts. These catalysts are configured to react with either cations or anions, provided in a feed stream. The flow electrodes allow using the same system for different feed streams, e.g., by flowing different types of electrodes through the system. Furthermore, the flow electrodes allow in-situ catalyst reconditioning. For example, the active particles can be flown from the current collectors to respective recovery devices where the particles are discharged or subjected to a reverse potential. The active particles can be conductive and provide more desirable electrical field distribution between the current collectors resulting in greater ionic mobility. Finally, the active particles concentrate ions around the particles thereby providing a higher concentration gradient through separating structures, which enclose the feed stream.

In this disclosure, a process of recycling acid, base and the salt reagents required in the Li recovery process is introduced. A membrane electrolysis cell which incorporates an oxygen depolarized cathode is implemented to generate the required chemicals onsite. The system can utilize a portion of the salar brine or other lithium-containing brine or solid waste to generate hydrochloric or sulfuric acid, sodium hydroxide and carbonate salts. Simultaneous generation of acid and base allows for taking advantage of both chemicals during the conventional Li recovery from brines and mineral rocks. The desalinated water can also be used for the washing steps on the recovery process or returned into the evaporation ponds. The method also can be used for the direct conversion of lithium salts to the high value LiOH product. The method does not produce any solid effluent which makes it easy-to-adopt for use in existing industrial Li recovery plants.

Methods, apparatuses, and systems related to the electrochemical separation of target gases from gas mixtures are provided. In some cases, a target gas such as carbon dioxide is captured and optionally released using an electrochemical cell (e.g., by bonding to an electroactive species in a reduced state). Some embodiments are particularly useful for selectively capturing the target gas while reacting with little to no oxygen gas that may be present in the gas mixture. Some such embodiments may be useful in applications involving separations from gas mixtures having relatively low concentrations of the target gas, such as direct air capture and ventilated air treatment.

Systems and methods for increasing the concentration of a desired CO.sub.x reduction reaction product are described. In some embodiments, the systems and methods include ethylene purification.

The electrochemical apparatus of the present disclosure includes a first stack that includes an oxide ion conductor as an electrolyte and decomposes water vapor to generate hydrogen and oxygen, a second stack that includes a proton conductor as an electrolyte and separates the hydrogen generated in the first stack from a gas mixture of the hydrogen and the water vapor that has not been decomposed in the first stack, and a heat insulation material that covers the first stack and the second stack.

The electrochemical apparatus of the present disclosure includes a first stack that includes an oxide ion conductor as an electrolyte and decomposes water vapor to generate hydrogen and oxygen, a second stack that includes a proton conductor as an electrolyte and separates the hydrogen generated in the first stack from a gas mixture of the hydrogen and the water vapor that has not been decomposed in the first stack, and a heat insulation material that covers the first stack and the second stack.

A process can be used for electrochemical preparation of an alkali metal alkoxide solution. The process is performed in an electrolysis cell having three chambers, where the middle chamber is separated from the cathode chamber by a solid-state electrolyte permeable to cations, for example NaSICON, and from the anode chamber by a diffusion barrier, for example a membrane selective for cations or anions. The process solves a problem where a concentration gradient forms in the middle chamber of the electrolysis cell during the electrolysis, which leads to locally lowered pH values and damage to the solid-state electrolyte used. This is prevented where a gas is introduced into the middle chamber during the electrolysis, which results in better mixing of the electrolyte solution in the middle chamber and prevents the formation of a concentration gradient.

In this disclosure, a process of recycling acid, base and the salt reagents required in the Li recovery process is introduced. A membrane electrolysis cell which incorporates an oxygen depolarized cathode is implemented to generate the required chemicals onsite. The system can utilize a portion of the salar brine or other lithium-containing brine or solid waste to generate hydrochloric or sulfuric acid, sodium hydroxide and carbonate salts. Simultaneous generation of acid and base allows for taking advantage of both chemicals during the conventional Li recovery from brines and mineral rocks. The desalinated water can also be used for the washing steps on the recovery process or returned into the evaporation ponds. The method also can be used for the direct conversion of lithium salts to the high value LiOH product. The method does not produce any solid effluent which makes it easy-to-adopt for use in existing industrial Li recovery plants.

In this disclosure, a process of recycling acid, base and the salt reagents required in the Li recovery process is introduced. A membrane electrolysis cell which incorporates an oxygen depolarized cathode is implemented to generate the required chemicals onsite. The system can utilize a portion of the salar brine or other lithium-containing brine or solid waste to generate hydrochloric or sulfuric acid, sodium hydroxide and carbonate salts. Simultaneous generation of acid and base allows for taking advantage of both chemicals during the conventional Li recovery from brines and mineral rocks. The desalinated water can also be used for the washing steps on the recovery process or returned into the evaporation ponds. The method also can be used for the direct conversion of lithium salts to the high value LiOH product. The method does not produce any solid effluent which makes it easy-to-adopt for use in existing industrial Li recovery plants.

Nanoplatelet forms of monolayer metal hydroxides are provided, as well as methods for preparing same. The nanoplatelets are suitable for use in antimicrobial compositions, for pressure treating lumber against wood rot, termites, and fungus, for water treatment for the removal of heavy metal contaminants, for the production of plasmonics devices, for the production of ore, or for the recovery of valuable metals in, e.g., fly ash ponds, mine tailings ponds, or other fluids containing the metal in ionic form. The nanoplatelet forms include copper hydroxide nanoplatelets.