Methods and systems for reducing impurity metal from a refinery electrolyte solution

US10208389B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-10208389-B2
Application numberUS-201514846142-A
CountryUS
Kind codeB2
Filing dateSep 4, 2015
Priority dateAug 26, 2015
Publication dateFeb 19, 2019
Grant dateFeb 19, 2019

How to read this patent

A practical reading order for non-experts. Skip the full description unless you need deep technical detail.

  1. Title

    What the patent document calls the invention.

  2. Abstract

    A short plain-language summary of the technical disclosure.

  3. Assignees and inventors

    Who owns or filed the patent and who is credited as inventor.

  4. Key dates

    Filing, priority, publication, and grant dates set the timeline.

  5. First independent claim

    The legal scope of protection — read this for what is actually claimed.

  6. CPC / IPC classifications

    Technology tags used to group this patent with similar filings.

  7. Citations and related patents

    Prior art links and similar publications in this corpus.

Abstract

Official abstract text for this publication.

Disclosed are methods for the reduction of impurity metals from a refinery electrolyte solution. Certain methods comprise contacting a refinery electrolyte solution comprising an impurity metal with a phosphate ester having a structure represented by: wherein R 1 comprises a linear, branched or cyclic alkyl or aryl group, and wherein the impurity metal is selected from the group consisting of iron, antimony, arsenic, bismuth, tin and combinations thereof.

First claim

Opening claim text (preview).

What is claimed is: 1. A method of reducing impurity metal from a refinery electrolyte solution, the method comprising contacting a refinery electrolyte solution comprising sulfuric acid and an impurity metal with a phosphate ester having a structure represented by: wherein R 1 comprises a linear, a C 6 -C 9 branched or a cyclic alkyl or aryl group, wherein the phosphate ester comprises iso-octyl phosphoric acid or a C 12 alkyl phenylphosphoric acid, and wherein the impurity metal is selected from the group consisting of iron, antimony, arsenic, bismuth, tin and combinations thereof. 2. The method of claim 1 , further comprising contacting the refinery electrolyte solution comprising an impurity metal with a di-substituted phosphate ester. 3. The method of claim 1 , further comprising contacting the electrolyte solution with a solubility modifier. 4. The method of claim 1 , further comprising contacting the electrolyte solution with a kinetic modifier. 5. The method of claim 1 , wherein the impurity metal is selected from the group consisting of bismuth, antimony, tin and combinations thereof. 6. The method of claim 1 , further comprising: contacting the refinery electrolyte solution with a modifier. 7. The method of claim 1 , wherein the stripped organic solution further comprises a di-substituted phosphate ester at a molar ratio of the phosphate ester to the di-substituted ester of about 20:1 to 0.1:1. 8. The method of claim 1 , wherein the stripped organic solution further comprises a trialkyl phosphate ester is selected from the group consisting of tributyl phosphate, trihexyl phosphate ester, trioctyl phosphate ester, and tripentyl phosphate ester. 9. A method of reducing impurity metal from a refinery electrolyte solution, the method comprising: a. bleeding a stream of electrolyte solution with impurities from a refinery process, the electrolyte solution with impurities comprising sulfuric acid and an impurity metal selected from the group consisting of iron, antimony, arsenic, bismuth, tin and combinations thereof; and b. mixing the electrolyte solution with impurities with a stripped organic solution to provide a loaded organic solution containing at least a portion of the impurities and electrolyte solution with reduced impurities, wherein the stripped organic solution comprises a phosphate ester having a structure represented by: wherein R 1 comprises a linear, a C 6 -C 9 branched or a cyclic alkyl or aryl group, and wherein the phosphate ester comprises iso-octyl phosphoric acid or a C 12 alkyl phenylphosphoric acid. 10. The method of claim 9 , further comprising mixing the loaded organic solution with a strip solution to provide a strip solution containing impurity metal and stripped organic. 11. The method of claim 10 , wherein the stripped organic is mixed with fresh electrolyte solution with impurities. 12. The method of claim 10 , wherein the strip solution containing the impurity metal is reused to be mixed with additional loaded organic solution. 13. The method of claim 9 , further comprising returning the electrolyte solution with reduced impurities to the refinery process. 14. The method of claim 9 , wherein mixing the electrolyte solution with impurities with a stripped organic solution comprises mixing in a mixing tank to provide an emulsion of the loaded organic solution and electrolyte solution with reduced impurities. 15. The method of claim 14 , further comprising separating the loaded organic solution and electrolyte solution with reduced impurities in a settler. 16. The method of claim 9 , further comprising: contacting the refinery electrolyte solution with a modifier. 17. The method of claim 9 , wherein the stripped organic solution further comprises a di-substituted phosphate ester at a molar ratio of the phosphate ester to the di-substituted ester of about 20:1 to 0.1:1. 18. A method of reducing impurity metal from a refinery electrolyte solution, the method comprising: a. bleeding a stream of electrolyte solution with impurities from a copper refinery process, the electrolyte solution with impurities comprising sulfuric acid and an impurity metal selected from the group consisting of iron, antimony, arsenic, bismuth, tin and combinations thereof; b. mixing in a mixing tank the electrolyte solution with impurities with a stripped organic solution to provide an emulsion comprising a loaded organic solution containing at least a portion of the impurities and electrolyte solution with reduced impurities, wherein the stripped organic solution comprises a phosphate ester having a structure represented by: wherein R 1 comprises a linear, C 6 -C 9 branched or cyclic alkyl or aryl group, wherein the phosphate ester comprises iso-octyl phosphoric acid or a C 12 alkyl phenylphosphoric acid; c. separating the loaded organic solution and electrolyte solution with reduced impurities in a settler; d. returning the electrolyte with reduced impurities to the copper refinery process; e. mixing in a mixing tank the loaded organic solution and a strip solution to provide an emulsion comprising a strip solution containing the impurity metal and stripped organic; and f. separating the strip solution containing the impurity metal and stripped organic. 19. The method of claim 18 , further comprising: contacting the refinery electrolyte solution with a modifier. 20. The method of claim 18 , wherein the stripped organic solution further comprises a di-substituted phosphate ester at a molar ratio of the phosphate ester to the di-substituted ester of about 20:1 to 0.1:1.

Assignees

Inventors

Classifications

  • in inorganic alkaline solutions · CPC title

  • C25C1/12Primary

    of copper · CPC title

  • C25C7/06Primary

    Operating or servicing · CPC title

  • with acids or salts thereof · CPC title

  • Recycling · CPC title

Patent family

Related publications grouped by family.

External sources

Frequently asked questions

Answers are generated from the same data shown on this page.

What does patent US10208389B2 cover?
Disclosed are methods for the reduction of impurity metals from a refinery electrolyte solution. Certain methods comprise contacting a refinery electrolyte solution comprising an impurity metal with a phosphate ester having a structure represented by: wherein R 1 comprises a linear, branched or cyclic alkyl or aryl group, and wherein the impurity metal is selected fr…
Who is the assignee on this patent?
Basf Se
What technology area does this patent fall under?
Primary CPC classification C25C1/12. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Feb 19 2019 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).