Acid mist suppression in copper electrowinning
US-12098474-B2 · Sep 24, 2024 · US
US12448695B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-12448695-B2 |
| Application number | US-202217847301-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jun 23, 2022 |
| Priority date | Jun 23, 2022 |
| Publication date | Oct 21, 2025 |
| Grant date | Oct 21, 2025 |
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A metal recovery device for recovering metal in a waste printed circuit board by way of electrodeposition including: a cathode, an anode, and an electrolyte in electrical communication with the cathode and the anode, wherein the electrolyte includes a glycol-based compound and a metal chloride. A method of preparing an electrolyte for use in the same. A method of metal recovery for recovering metal from waste printed circuit board by making use the same.
Opening claim text (preview).
The invention claimed is: 1. A metal recovery device for recovering metal in a waste printed circuit board by way of electrodeposition comprising: a cathode, an anode, and an electrolyte in electrical communication with the cathode and the anode, wherein the anode, consists of porous reticulated vitreous carbon which exhibits a honeycomb arrangement, is adapted to facilitate the capture of the metal in the waste printed circuit board to undergo oxidative leaching, and the electrolyte comprises a chelating agent of glycol-based compound and potassium chloride to prevent precipitation of the metal ions and maintain the metal ions available for cathodic reductive deposition. 2. The metal recovery device according to claim 1 , wherein the glycol-based compound is a petrochemical. 3. The metal recovery device according to claim 1 , wherein the glycol-based compound is a monomeric glycol. 4. The metal recovery device according to claim 3 , wherein the monomeric glycol is ethylene glycol. 5. The metal recovery device according to claim 3 , wherein the monomeric glycol is propylene glycol. 6. The metal recovery device according to claim 1 , wherein the porous reticulated vitreous carbon has a porosity from about 10 ppi to about 100 ppi. 7. The metal recovery device according to claim 1 , wherein the porous reticulated vitreous carbon is submerged in the electrolyte at a predetermined submerged depth which is determined with reference to the porosity of the anode. 8. The metal recovery device according to claim 1 , wherein the cathode comprises a cathode material selected from a group consisting of nickel, copper, iron, nickel foam, copper foam, aluminum foam, carbon cloth, carbon foam, and a combination thereof. 9. The metal recovery device according to claim 8 , wherein the cathode material is covered by a substantially porous structure. 10. The metal recovery device according to claim 9 , wherein the substantially porous structure has a porosity from about 100 mesh to about 200 mesh. 11. The metal recovery device according to claim 9 , wherein the substantially porous structure comprises a material selected from a group consisting of cotton cloth, porous carbon cloth, plastic cloth and a combination thereof. 12. The metal recovery device according to claim 1 , wherein the electrodeposition is conducted at a current density from about 0.2 mA cm −2 to about 300 mA cm −2 . 13. The metal recovery device according to claim 1 , wherein the metal recovered is a heavy metal. 14. The metal recovery device according to claim 13 , wherein the heavy metal is copper. 15. The metal recovery device according to claim 1 , wherein the electrolyte further comprises NH 4 Cl. 16. The metal recovery device according to claim 1 , wherein the electrolyte is reusable for two or more electrodeposition cycles. 17. The metal recovery device according to claim 16 , wherein sensitivity of the device is between about 50% to about 60% in each electrodeposition cycle. 18. The metal recovery device according to claim 16 , wherein the sensitivity of the device increases with a number of cycles the electrolyte is reused. 19. The metal recovery device according to claim 18 , wherein the device has a sensitivity of about 60% when the electrolyte is reused for three electrodeposition cycles. 20. The metal recovery device according to claim 18 , wherein the number of cycles the electrolyte is reused is proportional to cathodic Faradaic efficiency of the device. 21. The metal recovery device according to claim 20 , wherein the cathodic Faradaic efficiency of the device is at about 99%, when the electrolyte is reused for three electrodeposition cycles. 22. The metal recovery device according to claim 16 , wherein metal selectivity of the device is at least 50% in each electrodeposition cycle. 23. The metal recovery device according to claim 16 , wherein metal recovery of the device is between about 26% to about 70% in each electrodeposition cycle.
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