Acid mist suppression in copper electrowinning
US-12098474-B2 · Sep 24, 2024 · US
US2023416936A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2023416936-A1 |
| Application number | US-202217847301-A |
| Country | US |
| Kind code | A1 |
| Filing date | Jun 23, 2022 |
| Priority date | Jun 23, 2022 |
| Publication date | Dec 28, 2023 |
| Grant date | — |
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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.
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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 electrolyte comprises a glycol-based compound and a metal chloride. 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 anode comprises an anode material selected from a group consisting of porous carbon material, metal foam, conductive polymer foam and a combination thereof. 7 . The metal recovery device according to claim 6 , wherein the porous carbon material is selected from a group consisting of reticulated vitreous carbon, carbon nanotube foam, graphene foam, graphite foam, carbon cloth, carbon paper and a combination thereof. 8 . The metal recovery device according to claim 1 , wherein the anode being reticulated vitreous carbon with a porosity from about 10 ppi to about 100 ppi. 9 . The metal recovery device according to claim 1 , wherein depth of the anode submerged in the electrolyte varies with the porosity of the anode. 10 . 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. 11 . The metal recovery device according to claim 10 , wherein the cathode material is covered by a substantially porous structure. 12 . The metal recovery device according to claim 11 , wherein the substantially porous structure has a porosity from about 100 mesh to about 200 mesh. 13 . The metal recovery device according to claim 11 , 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. 14 . 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 . 15 . The metal recovery device according to claim 1 , wherein the metal comprises heavy metal. 16 . The metal recovery device according to claim 15 , wherein the heavy metal is copper. 17 . The metal recovery device according to claim 1 , wherein the metal chloride is potassium chloride. 18 . The metal recovery device according to claim 1 , wherein the electrolyte further comprises NH 4 Cl. 19 . The metal recovery device according to claim 1 , wherein the electrolyte is reusable for two or more electrodeposition cycles. 20 . The metal recovery device according to claim 19 , wherein sensitivity of the device is between about 50% to about 60% in each electrodeposition cycle. 21 . The metal recovery device according to claim 19 , wherein reuse of the electrolyte increases amount of metal recovered in each electrodeposition cycle. 22 . The metal recovery device according to claim 21 , wherein the device has a sensitivity of about 60% when the electrolyte is being reused for three electrodeposition cycles. 23 . The metal recovery device according to claim 21 , wherein cathodic Faradaic efficiency of the device in each electrodeposition cycle increases with number of cycles the electrolyte being reused. 24 . The metal recovery device according to claim 23 , wherein the cathodic Faradaic efficiency of the device is at about 99%, when the electrolyte is being reused for three electrodeposition cycles. 25 . The metal recovery device according to claim 1 , wherein the electrodeposition cycle has a metal selectivity of at least 50%. 26 . The metal recovery device according to claim 1 , wherein the electrodeposition cycle has a metal recovery from about 26% to about 70%. 27 . A method of preparing an electrolyte for use in the metal recovery device as claimed in claim 1 for recovering metal by way of electrodeposition, comprising the steps of: a) mixing a glycol-based compound with a metal chloride to form a substantially pH-neutral mixture; and b) contacting the substantially pH-neutral mixture with a desirable amount of sample to form a slurry. 28 . The method according to claim 27 , further comprising the step of preparing the sample by way of size reduction. 29 . The method according to claim 28 , wherein the size reduction comprising the step of blending the sample to powder form. 30 . The method according to claim 29 , wherein the powder form of the sample is of about 100 mesh to about 200 mesh. 31 . The method according to claim 27 , wherein concentration of the sample in the electrolyte is about 1 mg/L to about 25 mg/L. 32 . A method of metal recovery for recovering metal from waste printed circuit board by making use of the metal recovery device as claimed in claim 1 , comprising the step of: conducting a first electrodeposition cycle with a current density of about 0.2 mA cm −2 to about 300 mA cm −2 for a cycle. 33 . The method according to claim 32 , wherein the electrodeposition is conducted at room temperature and atmospheric pressure. 34 . The method according to claim 32 , wherein the electrodeposition is conducted for at least 30 min. 35 . The method according to claim 32 , further comprising the step of conducting a second electrodeposition cycle by reusing electrolyte of the first electrodeposition cycle. 36 . The method according to claim 35 , wherein amount of metal collected in the second electrodeposition cycle is higher than amount of metal collected in the first electrodeposition cycle. 37 . The method according to claim 36 , wherein metal being recovered is selected from the group consisting of copper, cadmium, palladium and a combination thereof.
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