Method for refining bismuth

US2021292927A1 · US · A1

Patent metadata
FieldValue
Publication numberUS-2021292927-A1
Application numberUS-201716317998-A
CountryUS
Kind codeA1
Filing dateJan 30, 2017
Priority dateJan 30, 2017
Publication dateSep 23, 2021
Grant date

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  1. Title

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  2. Abstract

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  5. First independent claim

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  6. CPC / IPC classifications

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Abstract

Official abstract text for this publication.

A method for refining bismuth is provided, which comprises recovering bismuth from a solution obtained after recovery of noble metals from a copper electrolytic slime.The method comprises:1) a neutralization step of adding alkali to an acid solution to adjust the pH to the range of 2.0 or more and 3.0 or less, and then performing solid-liquid separation to obtain a neutralized filtrate and a neutralized precipitate;2) an alkaline leaching step of adding alkali to the neutralized precipitate obtained in the neutralization step to separate the resultant into an alkali leachate and an alkaline leaching residue;3) a sulfuric acid leaching step of adding sulfuric acid to the alkaline leaching residue to separate the resultant into a sulfuric acid leachate and a sulfuric acid-leaching residue;4) a cooling step of cooling the sulfuric acid leachate obtained in the sulfuric acid leaching step to obtain crystals of bismuth sulfate;5) a bismuth oxidation step of adding alkali to the crystals of bismuth sulfate obtained in the cooling step to obtain bismuth oxide; and6) an electrolysis step of adding an acid solution to the bismuth oxide obtained in the bismuth oxidation step for dissolution and then electrowinning the thus obtained solution to obtain metal bismuth.

First claim

Opening claim text (preview).

1 . A method for refining bismuth, comprising, in steps of smelting minerals containing copper, noble metals, bismuth and an impurity to obtain blister copper, subjecting the blister copper to electrolytic refining to recover copper, performing electrolytic refining to generate an electrolytic slime, and then recovering noble metals by a wet method from the electrolytic slime, subjecting an acid solution generated after recovery of the noble metals to the following steps: 1 ) a neutralization step of adding alkali to the acid solution to adjust the pH to a range of 2.0 or more and 3.0 or less, and then performing solid-liquid separation to obtain a neutralized filtrate and a neutralized precipitate; 2 ) an alkaline leaching step of adding alkali to the neutralized precipitate to separate the resultant into an alkali leachate and an alkaline leaching residue; 3 ) a sulfuric acid leaching step of adding sulfuric acid to the alkaline leaching residue to separate the resultant into a sulfuric acid leachate and a sulfuric acid-leaching residue; 4 ) a cooling step of cooling the sulfuric acid leachate to obtain crystals of bismuth sulfate; 5 ) a bismuth oxidation step of adding alkali to the crystals of bismuth sulfate to obtain bismuth oxide; and 6 ) an electrolysis step of adding an acid solution to the bismuth oxide for dissolution, and then electrowinning the thus obtained solution to obtain metal bismuth. 2 . The method for refining bismuth according to claim 1 , wherein the impurity is one or more types of copper, iron, lead, arsenic, and tellurium. 3 . The method for refining bismuth according to claim 1 , comprising a boiling step of heating the alkali leachate obtained in the alkaline leaching step at 90° C. or higher, and then cooling the resultant to obtain crystals containing arsenic. 4 . The method for refining bismuth according to claim 1 , wherein the sulfuric acid leaching step comprises a two-stage leaching process of: first contacting with low-concentration sulfuric acid to leach a leaching residue, so as to separate the resultant into a primary leachate and a primary leaching residue; and then contacting the primary leaching residue with high-concentration sulfuric acid, so as to separate the resultant into a secondary leachate and a secondary leaching residue, and then feeding the thus obtained secondary leachate to the cooling step. 5 . The method for refining bismuth according to claim 1 , wherein the acid solution to be used in the electrolysis step is a solution containing hydrosilicofluoric acid. 6 . The method for refining bismuth according to claim 1 , wherein in the alkaline leaching step, alkali to be added to the neutralized precipitate is a sodium hydroxide solution with a concentration of 1 mol/l or more and 5 mol/l or less, and the sodium hydroxide solution is used and mixed with the precipitate for dissolution in such a manner that the slurry concentration is a range of 10 g/l or more and 100 g/l or less, so as to obtain an alkali leachate and an alkaline leaching residue. 7 . The method for refining bismuth according to claim 1 , comprising, in the sulfuric acid leaching step, adjusting the pH of the slurry after addition of sulfuric acid to the range of 0 or more and 3.5 or less, and then performing solid-liquid separation, so as to obtain a sulfuric acid leachate and a sulfuric acid-leaching residue.

Assignees

Inventors

Classifications

  • C22B30/06Primary

    Obtaining bismuth · CPC title

  • C25C1/22Primary

    of metals not provided for in groups C25C1/02 - C25C1/20 · CPC title

  • C22B7/006Primary

    Wet processes · CPC title

  • by acid leaching · CPC title

  • of copper · CPC title

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What does patent US2021292927A1 cover?
A method for refining bismuth is provided, which comprises recovering bismuth from a solution obtained after recovery of noble metals from a copper electrolytic slime.The method comprises:1) a neutralization step of adding alkali to an acid solution to adjust the pH to the range of 2.0 or more and 3.0 or less, and then performing solid-liquid separation to obtain a neutralized filtrate and a ne…
Who is the assignee on this patent?
Sumitomo Metal Mining Co
What technology area does this patent fall under?
Primary CPC classification C22B30/06. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Thu Sep 23 2021 00:00:00 GMT+0000 (Coordinated Universal Time) (A1). 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).