Methods and systems related to augmenting syngas production using electrolysis are disclosed. A disclosed method includes harvesting a volume of carbon monoxide from a syngas production system operating on a volume of natural gas, supplying the volume of carbon monoxide to a cathode area of an electrolyzer, and generating, using the volume of carbon monoxide and the electrolyzer, a volume of generated chemicals. The volume of generated chemicals is at least one of: a volume of hydrocarbons, a volume of olefins, a volume of organic acids, a volume of alcohols, and a volume of N-rich organic compounds.

An electrochemical process, and related method and system to upgrade captured CO.sub.2 into value-added products. CO.sub.2 capture technologies based on chemisorption present the potential to lower net emissions of CO.sub.2 into the atmosphere. The use of alkali cations to tailor the electrochemical double layer allows achieving the valorization of chemisorbed CO.sub.2 in an aqueous amine-based electrolyte, by placing the CO.sub.2 of the amine-CO.sub.2 adduct sufficiently close to the site of an heterogeneous reaction at the working electrode. It is revealed, using electrochemical studies and in-situ surface-enhanced Raman spectroscopy, that a smaller double layer distance can correlate with improved activity for CO.sub.2 to CO from amine solutions.

An electrochemical process, and related method and system to upgrade captured CO.sub.2 into value-added products. CO.sub.2 capture technologies based on chemisorption present the potential to lower net emissions of CO.sub.2 into the atmosphere. The use of alkali cations to tailor the electrochemical double layer allows achieving the valorization of chemisorbed CO.sub.2 in an aqueous amine-based electrolyte, by placing the CO.sub.2 of the amine-CO.sub.2 adduct sufficiently close to the site of an heterogeneous reaction at the working electrode. It is revealed, using electrochemical studies and in-situ surface-enhanced Raman spectroscopy, that a smaller double layer distance can correlate with improved activity for CO.sub.2 to CO from amine solutions.

The current disclosure provides alternating current based systems and methods to develop chemical compounds, such as drug molecules using electrochemistry in organic synthesis.

The current disclosure provides alternating current based systems and methods to develop chemical compounds, such as drug molecules using electrochemistry in organic synthesis.

A modified electrode, manufacturing method thereof and use thereof are provided. The manufacturing method includes steps of soaking a copper substrate in a solution to obtain a BiOI/copper(I) iodide, BiOI/copper(I) iodide/metallic bismuth, and copper(I) iodide/metallic bismuth composite modified electrodes by electroless plating method. The obtained electrodes, designated as bismuth-based modified electrode, can be used for the electrohydrodimerization of acrylonitrile to synthesize adiponitrile.

A modified electrode, manufacturing method thereof and use thereof are provided. The manufacturing method includes steps of soaking a copper substrate in a solution to obtain a BiOI/copper(I) iodide, BiOI/copper(I) iodide/metallic bismuth, and copper(I) iodide/metallic bismuth composite modified electrodes by electroless plating method. The obtained electrodes, designated as bismuth-based modified electrode, can be used for the electrohydrodimerization of acrylonitrile to synthesize adiponitrile.

The present invention relates to a method for preparing primary diamines from amino acid compounds. Specifically, this invention is related to the preparation of a primary diamine from an amino acid and/or its salt by Kolbe electrolysis coupling reaction.

The present invention relates to an electrochemical method for converting an amino acid and/or its salts to an amine and/or a nitrile. The total yield and selectivity of amine and nitrile obtained by the method according to the present invention is higher than prior art when the reaction medium has a high concentration of amino acid and/or its salts at the beginning of the reaction.

The present invention relates to an electrochemical method for converting an amino acid and/or its salts to an amine and/or a nitrile. The total yield and selectivity of amine and nitrile obtained by the method according to the present invention is higher than prior art when the reaction medium has a high concentration of amino acid and/or its salts at the beginning of the reaction.