US2016222487A1PendingUtilityA1
Recovery of metals
Est. expirySep 16, 2033(~7.2 yrs left)· nominal 20-yr term from priority
C22B 7/007C22B 25/06C22B 11/046C22B 13/045C22B 15/0069C23F 1/30Y02P10/20
42
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Claims
Abstract
A method for recovering metal from electronic waste contacting electronic waste with a recovery solution to dissolve metals from the electronic waste into the recovery solution, wherein the recovery solution comprises nitric acid and ferric nitrate; and raising the pH of the recovery solution to precipitate at least some of said metals therefrom.
Claims
exact text as granted — not AI-modified1 . A method for recovering metal from electronic waste, the method comprising;
contacting electronic waste with a recovery solution to dissolve metals from the electronic waste into the recovery solution, wherein the recovery solution comprises nitric acid and ferric nitrate; and raising the pH of the recovery solution to precipitate at least some of said metals therefrom.
2 . The method of claim 1 , wherein the recovery solution comprises from 0.5 to 12 wt % ferric nitrate.
3 . The method of claim 1 , wherein the recovery solution comprises from 10 to 60 wt % nitric acid, preferably from 15 to 40 wt %.
4 . The method of claim 1 , wherein the recovery solution comprises chloride ions.
5 . The method of claim 1 , wherein the recovery solution further comprises sulphamate ions.
6 . The method of claim 1 , wherein the recovery solution further comprises a copper corrosion inhibitor.
7 . The method of claim 1 , further comprising subjecting the recovery solution and electronic waste to agitation with an oxygen-containing gas.
8 . The method according to claim 1 , wherein the electronic waste is immersed for at least 30 minutes in the recovery solution.
9 . The method of claim 1 , further comprising adding chloride ions to the recovery solution prior to raising the pH.
10 . The method of claim 1 , wherein the raising the pH of the recovery solution comprises raising the pH to from 3 to 6.
11 . The method of claim 1 , further comprising:
(i) raising the pH to from 3 to 6; (ii) raising the pH to greater than 6; and (iii) lowering the pH to from 3 to 6,
wherein precipitate formed by steps (i), (ii) and (iii) is recovered from the recovery solution before the next step.
12 . The method of claim 1 , wherein contacting the electronic waste with the recovery solution is carried out in a revolving drum.
13 . The method of claim 1 , further comprising continuous filtration of the recovery solution.
14 . The method of claim 1 , wherein method is a batch process and the recovery solution is regenerated with nitric acid between batches.
15 . The method according to claim 1 , wherein the electronic waste comprises circuit-board waste.
16 . The method according to any claim 1 , wherein the electronic waste is contacted with a recovery solution having a pH of less than 1.
17 . The method according to claim 1 , the method further comprising removing any electronic waste residue from the recovery solution before raising the pH.
18 . The method according to claim 1 , wherein the electronic waste is not provided in the form of a powder.
19 . The method according to claim 1 , wherein the step of raising the pH is conducted stepwise to allow for the separate precipitation and recovery of different metals.
20 . The method according to claim 1 , wherein the metals recovered comprise one or more of lead, silver, iron, copper, gold, zinc and tin.
21 . The method of claim 1 , further comprising recovering the precipitated metals from the recovery solution.
22 . The method according to claim 1 , the method further comprising subjecting the precipitated metals to further treatment to recover one or more substantially pure metals.
23 . The method according to claim 1 , wherein the method comprises additionally recovering and sorting electronic components separated from the electronic waste by the dissolution of metal from the electronic waste.
24 . The method of claim 1 , wherein:
the metals recovered comprise tin; the recovery solution and electronic waste are subjected to air agitation; the pH is raised to from 3 to 6; and the recovery solution comprises:
from 1 to 3.5 wt % ferric nitrate;
from 15 to 40 wt % nitric acid;
from 0.5 to 2 wt % chloride ions;
from 1 to 10 wt % ammonium sulphamate; and
from 0.01 to 0.5 wt % benzotriazole.Join the waitlist — get patent alerts
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