Electrolyte tank volume rebalancing
US-2024396064-A1 · Nov 28, 2024 · US
US2024363881A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2024363881-A1 |
| Application number | US-202218685969-A |
| Country | US |
| Kind code | A1 |
| Filing date | Aug 23, 2022 |
| Priority date | Aug 23, 2021 |
| Publication date | Oct 31, 2024 |
| Grant date | — |
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The invention provides methods of electrochemically rebalancing electrochemical systems such as flow batteries and electrochemical CO 2 capture systems. Electrochemical imbalances due to reaction with molecular oxygen can lead to capacity loss. The loss of capacity may be mitigated by electrically oxidizing the excess hydroxide ions to produce gaseous O 2 , which can be removed by de-gassing methods.
Opening claim text (preview).
What is claimed is: 1 . A method of rebalancing an electrochemical device comprising the steps of: a) providing an electrochemical device comprising a negolyte comprising a first redox active species having a reduced form and an oxidized form in contact with a first electrode, a posolyte comprising a second redox active species having a reduced form and an oxidized form in contact with a second electrode, and a barrier separating the negolyte and posolyte, wherein when the electrochemical device is charged, the reduced form of the first redox active species reacts with molecular oxygen to form the oxidized form of the first redox active species while the second redox active species remains in the oxidized form, thereby electrochemically unbalancing the electrochemical device; and wherein a discharge reaction or reaction with molecular oxygen produces an OH − ion; and b) applying an electrical pulse across the electrochemical device sufficient to produce a gaseous oxidation product in the negolyte. 2 . The method of claim 1 , wherein the electrical pulse reverts the oxidized form of the second redox active species to the reduced form of the second redox active species. 3 . The method of claim 1 , further comprising (c) removing the gaseous oxidation product. 4 . The method of claim 1 , wherein the electrical pulse is applied every 100 cycles. 5 . The method of claim 3 , wherein the gaseous oxidation product is removed by flowing a carrier gas through the electrochemical device or by applying negative pressure. 6 . The method of claim 1 , wherein the electrical pulse lowers the pH of the negolyte. 7 . The method of claim 1 , wherein step (a) further comprises monitoring a capacity of the electrochemical device or a pH of the negolyte to determine when to apply the pulse of step (b). 8 . The method of claim 7 , wherein step the pulse of step (b) is applied when the pH is greater than 9. 9 . The method of claim 7 , wherein the pulse of step (b) is applied when the pH is about 14. 10 . The method of claim 7 , wherein the pulse of step (b) is applied when the capacity is below 90% of an initial capacity. 11 . The method of claim 1 , wherein the electrochemical device provided is a battery and step (a) further comprises: i) charging the battery, and ii) connecting a load to the first and second electrodes and allowing the battery to discharge. 12 . The method of claim 11 , wherein step (b) comprises biasing the battery at a voltage more negative than a discharging voltage of the battery. 13 . The method of claim 11 , wherein the gaseous oxidation product is molecular oxygen and step (b) comprises oxidizing OH − or H 2 O in the negolyte to molecular oxygen. 14 . The method of claim 1 , wherein the electrochemical device is a carbon capture cell and step (a) further comprises: i) applying a voltage across the first and second electrodes to charge the electrochemical device and produce OH − ions; ii) providing a source of CO 2 to the negolyte to dissolve CO 2 and react it with the OH − ions; and iii) connecting a load to the first and second electrodes and allowing the electrochemical device to discharge and release CO 2 . 15 . The method of claim 1 , wherein the first and second redox active species have the same reduced and oxidized forms. 16 . The method of claim 1 , wherein the first and second redox active species have different reduced and oxidized forms.
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