The present disclosure relates to an electrochemical flow cell that includes a gap positioned between an ion exchange membrane (IEM) and a cathode gas diffusion electrode (GDE), where the gap is positioned to contain a liquid and the gap has a thickness value, as defined by the distance between the IEM and the cathode GDE, of between greater than zero mm and less than about 2.0 mm. In some embodiments of the present disclosure, the gap may be between about 0.1 mm and about 1.0 mm.

The present disclosure relates to an electrochemical flow cell that includes a gap positioned between an ion exchange membrane (IEM) and a cathode gas diffusion electrode (GDE), where the gap is positioned to contain a liquid and the gap has a thickness value, as defined by the distance between the IEM and the cathode GDE, of between greater than zero mm and less than about 2.0 mm. In some embodiments of the present disclosure, the gap may be between about 0.1 mm and about 1.0 mm.

The invention concerns a process for the electrochemical production of formate. The process is performed in an electrochemical cell comprising a cathode compartment containing a cathode, an anode compartment containing a nickel-based anode and an ion exchange membrane separating the anode compartment from the cathode compartment. The process comprises the following steps: (a) feeding an anolyte comprising at least one polyol to the anode compartment; (b) feeding a catholyte comprising CO.sub.2 to the cathode compartment; (c) and applying a voltage difference between the cathode and the anode such that at the cathode CO.sub.2 is reduced to formate and at the anode the at least one polyol is oxidized to formate.

The invention concerns a process for the electrochemical production of formate. The process is performed in an electrochemical cell comprising a cathode compartment containing a cathode, an anode compartment containing a nickel-based anode and an ion exchange membrane separating the anode compartment from the cathode compartment. The process comprises the following steps: (a) feeding an anolyte comprising at least one polyol to the anode compartment; (b) feeding a catholyte comprising CO.sub.2 to the cathode compartment; (c) and applying a voltage difference between the cathode and the anode such that at the cathode CO.sub.2 is reduced to formate and at the anode the at least one polyol is oxidized to formate.

Disclosed is a process for preparing adiponitrile from acrylonitrile in an electrolytic cell. An aqueous electrolyte comprising acrylonitrile converts to adiponitrile in the presence of a solid anode and in the absence of a solid cathode. The cathode comprises gas plasma.

Disclosed is a process for preparing adiponitrile from acrylonitrile in an electrolytic cell. An aqueous electrolyte comprising acrylonitrile converts to adiponitrile in the presence of a solid anode and in the absence of a solid cathode. The cathode comprises gas plasma.

A system and method for treating flue gas of a boiler based on solar energy are provided, wherein a heat pump is connected with a heat collector via first and second valves, a carbon dioxide electrolysis chamber is connected with a flue gas pretreatment chamber and a power distribution control module for electrolyzing and reducing carbon dioxide, a gas phase separation chamber is connected with a gas phase outlet to separate a mixture, and discharge the separated gas phase products; a Fischer-Tropsch reaction chamber is connected with the gas phase separation chamber to pass the separated carbon monoxide and hydrogen into a flowing reaction cell, a liquid phase product separation chamber is connected with a liquid phase outlet to separate the liquid phase hydrocarbon fuel products, and separate and supplement electrolyte; an electrolyte cooling circulation chamber is connected with the liquid phase product separation chamber.

Anion exchange polymers having high OH.sup.− conductivity, chemical stability, and mechanical stability have been developed for use in AEMs. The anion exchange polymers have stable hydrophobic polymer backbones, stable hydrophilic quaternary ammonium cationic groups, and hydrophilic phenolic hydroxyl groups on the polymer side chains. The polymers have polymer backbones free of ether bonds, hydrophilic polymer side chains, and piperidinium ion-conducting functionality, which enables efficient and stable operation in water or CO.sub.2 electrolysis, redox flow battery, and fuel cell applications. The polymer comprises a plurality of repeating units of formula (I)

##STR00001##

Anion exchange membranes and membrane electrode assemblies incorporating the anion exchange polymers are also described.

Anion exchange polymers having high OH.sup.− conductivity, chemical stability, and mechanical stability have been developed for use in AEMs. The anion exchange polymers have stable hydrophobic polymer backbones, stable hydrophilic quaternary ammonium cationic groups, and hydrophilic phenolic hydroxyl groups on the polymer side chains. The polymers have polymer backbones free of ether bonds, hydrophilic polymer side chains, and piperidinium ion-conducting functionality, which enables efficient and stable operation in water or CO.sub.2 electrolysis, redox flow battery, and fuel cell applications. The polymer comprises a plurality of repeating units of formula (I)

##STR00001##

Anion exchange membranes and membrane electrode assemblies incorporating the anion exchange polymers are also described.

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.