Cost-effective method for recovering precious metals in circuit board components

US11753699B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-11753699-B2
Application numberUS-202217975606-A
CountryUS
Kind codeB2
Filing dateOct 28, 2022
Priority dateDec 3, 2021
Publication dateSep 12, 2023
Grant dateSep 12, 2023

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

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  6. CPC / IPC classifications

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  7. Citations and related patents

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Abstract

Official abstract text for this publication.

A cost-effective method for recovering precious metals in circuit board components utilizes the basic principle of oxidation-reduction reaction, adopts a mixed solution of sulfuric acid and hydrogen peroxide and a mixed solution of hydrochloric acid, sodium chloride and sodium chlorate, and also adopts ammonia water and formaldehyde to reduce silver. According to the characteristic that the redox potential of gold and palladium ions is higher, the gold and palladium ions in the chlorination leaching solution are selectively reduced into elements by using a reducing agent which is low in price and moderate in reducibility, then the elements are separated through filtration to realize resource recycling.

First claim

Opening claim text (preview).

We claim: 1. A cost-effective method for recovering precious metals in circuit board components, comprising following steps: (1) leaching: add metal powder after crushing and magnetic separation to a first mixed solution of sulfuric acid and hydrogen peroxide, and react at 70-90° C. for 2-3 hours; a liquid-solid ratio between the metal powder and the first mixed solution is 4:1-8:1; after filtration, filter residue is added with a second mixed solution of hydrochloric acid, sodium chloride and sodium chlorate to react at 70-90° C. for 2-3 hours to obtain a metal chloride leaching solution, a liquid-solid ratio of the metal chloride leaching solution is 5:1-9:1; (2) precipitation: the metal chloride leaching solution of step (1) is cooled to room temperature and filtered to obtain solid silver chloride, wherein the solid silver chloride is added into ammonia water and formaldehyde to obtain silver element; add an organic reducing agent to a filtrate obtained by cooling the metal chloride leaching solution to room temperature and filtering to react at 50-70° C. for 6-10 hours, filter out precipitation material, including gold, palladium and tin dioxide, after washed with hydrochloric acid, gold and palladium is obtained; (3) circulation: add an extractant to a filtrate obtained from the reaction of the organic reducing agent and the filtrate obtained by cooling and filtering the metal chloride leaching solution in step (2) for extraction, after extraction, an organic phase and a water phase are obtained, the extractant and the organic reducing agent are separated from the organic phase by decompression distillation, and the organic reducing agent is reused in step (2); add hydrochloric acid, sodium chlorate into the water phase until a concentration of hydrochloric acid, sodium chlorate and sodium chloride becomes equal to that of the second mixed solution in step (1) to obtain a recycled water phase; the recycled water phase is circulated back to step (1) to be reused as the second mixed solution, and the water phase after extraction and circulations is regarded as last tail liquor, sodium chloride is recovered from the tail gas by evaporative crystallization. 2. The cost-effective method for recovering precious metals in circuit board components according to claim 1 , wherein, in the first mixed solution of step (1): a concentration of sulfuric acid is 1.5 mol/L-3 mol/L, a mass percentage concentration of hydrogen peroxide is 20%-30%, and a volume ratio between sulfuric acid and hydrogen peroxide is 2:1-4:1. 3. The cost-effective method for recovering precious metals in circuit board components according to claim 1 , wherein, in the second mixed solution of step (1), the concentration of hydrochloric acid is 0.5-1.5 mol/L, the concentration of sodium chloride is 120-190 g/L, and the concentration of sodium chlorate is 6.82-20.46 g/L. 4. The cost-effective method for recovering precious metals in circuit board components according to claim 1 , wherein the organic reducing agent in step (2) is one or more of amide organic compounds. 5. The cost-effective method for recovering precious metals in circuit board components according to claim 1 , wherein the extractant in step (3) is one or more of dichloromethane, chloroform and benzene. 6. The cost-effective method for recovering precious metals in circuit board components according to claim 4 , wherein the organic reducing agent in step (2) is selected from N,N-Dimethylformamide (DMF) and N,N-dimethylacetamide (DMA).

Assignees

Inventors

Classifications

  • C22B11/046Primary

    from manufactured products, e.g. from printed circuit boards, from photographic films, paper or baths · CPC title

  • Recycling · CPC title

  • by acid leaching · CPC title

  • C22B7/005Primary

    Separation by a physical processing technique only, e.g. by mechanical breaking · CPC title

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What does patent US11753699B2 cover?
A cost-effective method for recovering precious metals in circuit board components utilizes the basic principle of oxidation-reduction reaction, adopts a mixed solution of sulfuric acid and hydrogen peroxide and a mixed solution of hydrochloric acid, sodium chloride and sodium chlorate, and also adopts ammonia water and formaldehyde to reduce silver. According to the characteristic that the red…
Who is the assignee on this patent?
Univ Beijing Technology
What technology area does this patent fall under?
Primary CPC classification C22B11/046. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Sep 12 2023 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).