Co2 electroreduction to multi-carbon products in strong acid
US-2024093390-A1 · Mar 21, 2024 · US
US2021230757A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2021230757-A1 |
| Application number | US-201917264505-A |
| Country | US |
| Kind code | A1 |
| Filing date | Aug 1, 2019 |
| Priority date | Aug 2, 2018 |
| Publication date | Jul 29, 2021 |
| Grant date | — |
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A metal sulfate manufacturing system comprising an electrochemical dissolution system having, an anode electrode that holds metal raw material, a cathode electrode, an electrolyte bath having an inlet to receive an initial acid or metal-acid complex solution and an outlet to discharge the treated metal sulfate solution, stirring equipment that mixes the electrolyte bath, a temperature control system, and a rectifier that supplies current at constant voltage between the anode and cathode electrode.
Opening claim text (preview).
What is claimed is: 1 . An electrochemical dissolution system for dissolving raw metal materials, comprising: an electrolyte bath container having an inlet, an outlet, a temperature control system, and configured to hold an electrolyte solution; a liquid permeable anode electrode disposed within the bath container; a cathode electrode surrounding the liquid permeable anode electrode; and a power supply electrically connected to the liquid permeable anode electrode and cathode electrode. 2 . The electrochemical dissolution system of claim 1 , wherein the cathode electrode surrounds the liquid permeable anode electrode equidistantly on all sides. 3 . The electrochemical dissolution system of claim 1 , further comprising an agitator configured to agitate electrolyte within the bath container. 4 . The electrochemical dissolution system of claim 1 , wherein the liquid permeable anode electrode comprises a basket-type shape, a sandwich-type shape, or a tray-type shape. 5 . The electrochemical dissolution system of claim 1 , wherein the liquid permeable anode electrode comprises at least one of platinum, platinum coated-titanium, and iridium coated-titanium. 6 . The electrochemical dissolution system of claim 1 , further comprising a metal raw material submerged within the electrolyte bath and held by the liquid permeable anode electrode. 7 . The electrochemical dissolution system of claim 6 , wherein the metal raw material comprises at least one of a nickel cathode, a nickel briquette, a cobalt cathode, and a cobalt briquette. 8 . The electrochemical dissolution system of claim 1 , wherein the liquid permeable anode electrode comprises an anode electrode body comprising at least one of a mesh type material and a punched type material. 9 . The electrochemical dissolution system of claim 1 , wherein the cathode electrode comprises at least one of platinum, platinum-coated nickel, and nickel. 10 . The electrochemical dissolution system of claim 1 , wherein the cathode electrode comprises a cathode electrode body comprising at least one of a corrugated-type material, a sponged-type material, and an embossed-type material. 11 . The electrochemical dissolution system of claim 1 , wherein the electrolyte bath container comprises an electrolyte. 12 . The electrochemical dissolution system of claim 11 , wherein the electrolyte comprises an acid. 13 . The electrochemical dissolution system of claim 12 , wherein the acid is sulfuric acid. 14 . The electrochemical dissolution system of claim 1 , wherein the acid concentration is between about 1M and about 3M. 15 . The electrochemical dissolution system of claim 1 , wherein the electrolyte bath agitator comprises at least one of a mechanical agitator, a magnetic stirrer, a liquid circulator, and an air agitator. 16 . A method of using the electrochemical dissolution system of claim 1 , comprising: applying a voltage between the liquid permeable and anode electrode and the cathode electrode; providing a fresh electrolyte solution to the electrolyte bath container through the inlet; and withdrawing a processed solution from the electrolyte bath container through the outlet. 17 . The method of claim 16 , wherein the fresh electrolyte solution has a metal concentration less than the processed solution. 18 . The method of claim 16 , further comprising controlling the temperature of the electrolyte bath container to between about 35° C. and about 60° C. using the temperature control system. 19 . The method of claim 16 , applying a voltage between about 2.0 V to about 3.5 V. 20 . The method of claim 16 , applying a voltage between about 0.1 V to about 1 V.
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