[go: up one dir, main page]

US1382494A - Purification of zinc solutions - Google Patents

Purification of zinc solutions Download PDF

Info

Publication number
US1382494A
US1382494A US431482A US43148220A US1382494A US 1382494 A US1382494 A US 1382494A US 431482 A US431482 A US 431482A US 43148220 A US43148220 A US 43148220A US 1382494 A US1382494 A US 1382494A
Authority
US
United States
Prior art keywords
zinc
solution
purification
mercury
salt
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
US431482A
Inventor
Field Samuel
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
METALS EXTRACTION Corp Ltd
Original Assignee
METALS EXTRACTION CORP Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by METALS EXTRACTION CORP Ltd filed Critical METALS EXTRACTION CORP Ltd
Priority to US431482A priority Critical patent/US1382494A/en
Application granted granted Critical
Publication of US1382494A publication Critical patent/US1382494A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22BPRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
    • C22B19/00Obtaining zinc or zinc oxide
    • C22B19/20Obtaining zinc otherwise than by distilling
    • C22B19/22Obtaining zinc otherwise than by distilling with leaching with acids
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P10/00Technologies related to metal processing
    • Y02P10/20Recycling

Definitions

  • the metal may be employed in granulated form or as powder, or other state of subdivision which is adapted to provide an extended contact surface.
  • 'zinc fume or blue powder may advantageously be used.
  • the zinc solution is acidified, and preferably also the process is carried out with application of heat.
  • the mercury salt may be added in any convenient way. It may beadded as a solution, or the required quantity of the salt itself may be directly dissolved in the zinc solution to be treated, or at a suitable prior stage in the preparation of the latter.
  • the salts of mercury utilizable include mercuric chlorid and mercuric nitrate, but it will be appreciated that if the zinc s subsequently to be deposited electrolytically the acid radical in the mercury salt must be of such a nature as not toattack the anodes and cause undue disintegration.
  • a suitable salt in this case is mercuric sulfate.
  • the metal or alloy used in conjunction with the mercury salt must be one whose presence in solution will not be detrimental to the electrolytic process.
  • zinc in a finely divided form is partlcularly suit able. alloy is used, a certain quantity of this metal passes into solution, but this is in no way 6 detrimental to the subsequent electro-deposi- When aluminium or an aluminium tion of the zinc. If desired, however, the aluminium may be subsequently removed concurrently with any iron impurity.
  • Crude zinc sulfate solutions such as the solutions obtained by'the treatment of a zinc ore, previously calcined, if necessary, with sulfuric acid or acid liquor from electrolytic cells, usually contains various foreign constituents, some of which, although present in very small amount, are nevertheless inadmissible if the solution is to be satisfactorily employed for electro-deposition.
  • These foreign constituents include salts of iron, arsenic, antimony, bismuth, copper, cadmium, nickel, cobalt and other less common metals which not infrequently occur in zinc bearing ores.
  • the present invention may be conveniently exemplified in its application in one way to the purification of a zinc solution of this kind for'the subsequent electrolytic deposition of the zinc, it being understood that this example is given for purpose of illustration and not by way of limitation.
  • the metallic impurities for example, copper, arsenic, antimony, bismuth, cadmium, nickel, cobalt and the rarer metals are precipitated upon the mercury in the form of a sludge which may be readily separated from the liquors by decantation or filtration.
  • This sludge may be subsequently treated in any. suitable way for recovery of the mercury, for example, by volatilization of the latter.
  • a considerable proportion of the zinc powder passes into solut1on and is therefore ultimately recovered by electrodeposition.
  • any iron present be not completely precipitated it may be removed by any suitable method either before or after the treatment just described.
  • Solutions purified by the process herein set forth are particularly suitable for the recovery of zinc by electro-deposition, but as will be readily understood the invention is equally applicable to the preparation of purified zinc solutions for other purposes.
  • the herein described process for the purification of a Zinc salt solution from foreign metals which comprises treating the acidified and heated solution with subdivided zinc in presence of a salt of mercury in the proportion of about 0.01 per cent. of mercury on the weight of'solution treated.

Landscapes

  • Engineering & Computer Science (AREA)
  • Chemical & Material Sciences (AREA)
  • Manufacturing & Machinery (AREA)
  • Materials Engineering (AREA)
  • Mechanical Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
  • Electrolytic Production Of Metals (AREA)
  • Manufacture And Refinement Of Metals (AREA)

Description

UNITED STATES PATENT OFFICE.
SAMUEL FIELD, OF LONDON, ENGLAND, ASSIGNOR TO THE METALS EXT-RAG- TION CORPORATION LIMITED, OF LONDON, ENGLAND, A. CORPORATION OF Patented June 21, 1921.
GUERNSEY.
PURIFICATION OF ZINC SOLUTIONS.
1,382,494 Specification of Letters Patent.
No Drawing. Application filed December 17, 1920. Serial N 0. 431,482.
T 0 all whom it may concern:
Be it known that I, SAMUEL FIELD, a subject of the King of England, residing at London, England, have invented certain new and .useful Improvementsin the Purification of Zinc Solutions, of which the following is a specification.
' This invention relates to the purification The metal may be employed in granulated form or as powder, or other state of subdivision which is adapted to provide an extended contact surface. For example, 'zinc fume or blue powder may advantageously be used.
Preferably the zinc solution is acidified, and preferably also the process is carried out with application of heat.
The mercury salt may be added in any convenient way. It may beadded as a solution, or the required quantity of the salt itself may be directly dissolved in the zinc solution to be treated, or at a suitable prior stage in the preparation of the latter.
The salts of mercury utilizable include mercuric chlorid and mercuric nitrate, but it will be appreciated that if the zinc s subsequently to be deposited electrolytically the acid radical in the mercury salt must be of such a nature as not toattack the anodes and cause undue disintegration. A suitable salt in this case is mercuric sulfate.
It is clear also that when the purified zinc solution is to be electrolyzed, the metal or alloy used in conjunction with the mercury salt must be one whose presence in solution will not be detrimental to the electrolytic process. For this purpose, therefore, zinc in a finely divided form is partlcularly suit able. alloy is used, a certain quantity of this metal passes into solution, but this is in no way 6 detrimental to the subsequent electro-deposi- When aluminium or an aluminium tion of the zinc. If desired, however, the aluminium may be subsequently removed concurrently with any iron impurity.
Crude zinc sulfate solutions such as the solutions obtained by'the treatment of a zinc ore, previously calcined, if necessary, with sulfuric acid or acid liquor from electrolytic cells, usually contains various foreign constituents, some of which, although present in very small amount, are nevertheless inadmissible if the solution is to be satisfactorily employed for electro-deposition.
These foreign constituents include salts of iron, arsenic, antimony, bismuth, copper, cadmium, nickel, cobalt and other less common metals which not infrequently occur in zinc bearing ores.
The present invention may be conveniently exemplified in its application in one way to the purification of a zinc solution of this kind for'the subsequent electrolytic deposition of the zinc, it being understood that this example is given for purpose of illustration and not by way of limitation.
To 10 tons of such a solution which has been brought to an acidity of 0.1 to 0.2 per cent, (for instance, by incomplete neutralization, or by complete neutralization for any special purpose, such as the removal of silica, and subsequent acidification with acid or acid liquors), 2 lbs. of mercury in the form of sulfate are added, and then about 40 lbs. of zinc powder, and the liquors are gently stirred while ,bein maintained at a temperature of 7O -1OO- As a first result of this treatment, mercury is deposited upon the zinc owder whic so constitutes a vigorous e ectro-chemical couple. The metallic impurities, for example, copper, arsenic, antimony, bismuth, cadmium, nickel, cobalt and the rarer metals are precipitated upon the mercury in the form of a sludge which may be readily separated from the liquors by decantation or filtration. This sludge may be subsequently treated in any. suitable way for recovery of the mercury, for example, by volatilization of the latter. A considerable proportion of the zinc powder passes into solut1on and is therefore ultimately recovered by electrodeposition.
If any iron present be not completely precipitated it may be removed by any suitable method either before or after the treatment just described.
15 into the solution,
Solutions purified by the process herein set forth are particularly suitable for the recovery of zinc by electro-deposition, but as will be readily understood the invention is equally applicable to the preparation of purified zinc solutions for other purposes.
In my prior United States specification,
Ser. No. 306,874, I have described a process for the purification of zinc solutions according to which the solutions were treated by present process amalgamation is actually brought about in the solution undergoing puri cation.
What I claim as my invention and desire to secure by Letters Patent is 1. The herein described process for the purification of a zinc salt solution from foreign metals, which comprises treating Athe solution with a sub-divided metal more electro-positive than the impurities to be removed, in presence of a salt of mercury.
2. The herein described process for the purification of a zinc salt solution from foreign metals, which comprises treating the solution with a sub-divided alloy more electro-positive than the impurities to be removed, in presence of a salt of mercury.
3. The herein described process for the purification of a zinc salt solution from foreign metals, which comprises treating the acidified solution with a sub-divided metal more electro-positive than the impurities to be removed, in presence of a salt of mercury.
4. The herein described process for the purlfication of a zinc salt solution from foreign metals, which comprises treating the acidified and heated solution with a subdivided metal more electro-positive than the impurities to be removed, in presence of a salt of mercury.
5. The herein described process for the purification of a zinc salt solution from foreign metals, which comprises treating the acidified and heated solution with subdivided zinc in presence of a salt of mercury.
6. The herein described process for the purification of a Zinc salt solution from foreign metals, which comprises treating the acidified and heated solution with subdivided zinc in presence of a salt of mercury in the proportion of about 0.01 per cent. of mercury on the weight of'solution treated.
7. The herein described process for the purification of a zinc salt solution from foreign metals, which comprises treating the acidified and heated solution with subdivided zinc, in presence of mercuric sulfate in the proportion of about 0.01 per cent. of mercury on the Weight of solution treated.
8. The herein described process for the purification of a zinc salt solution from foreign metals, which comprises bringing the solution to an acidity of 0.1 to 0.2 per cent, adding mercuric sulfate in the proportion of about 0.01 er cent. of mercury on the weight of solution treated, adding zinc powder and maintaining the solution at a temperature of 70l00 C.
In testimony whereof I affix my signature.
SAMUEL 'FIELD.
US431482A 1920-12-17 1920-12-17 Purification of zinc solutions Expired - Lifetime US1382494A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US431482A US1382494A (en) 1920-12-17 1920-12-17 Purification of zinc solutions

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US431482A US1382494A (en) 1920-12-17 1920-12-17 Purification of zinc solutions

Publications (1)

Publication Number Publication Date
US1382494A true US1382494A (en) 1921-06-21

Family

ID=23712136

Family Applications (1)

Application Number Title Priority Date Filing Date
US431482A Expired - Lifetime US1382494A (en) 1920-12-17 1920-12-17 Purification of zinc solutions

Country Status (1)

Country Link
US (1) US1382494A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2550805A1 (en) * 1983-08-17 1985-02-22 Asturienne France Process for the purification of zinc sulphate solutions for electrolytic zinc production, of the zinc cementation kind

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2550805A1 (en) * 1983-08-17 1985-02-22 Asturienne France Process for the purification of zinc sulphate solutions for electrolytic zinc production, of the zinc cementation kind

Similar Documents

Publication Publication Date Title
JPS604892B2 (en) How to recover metal from copper refining anode slime
US2187108A (en) Process of purifying lead nitrate solutions
US1382494A (en) Purification of zinc solutions
US1336386A (en) Purification of zinc solutions
US3419355A (en) Recovery of high purity selenium from selenium-bearing solutions containing metallicimpurities
US1887037A (en) Process of refining nickel bearing materials
US1351489A (en) Recovery of thorium
US2238437A (en) Process for recovering indium
US1496004A (en) Process of preparing pure zinc-sulphate solutions
US2031299A (en) Treating copper anode mud
US2241438A (en) Recovering indium
US2052387A (en) Treatment of indium-bearing materials
US2695227A (en) Indium purification using proteinaceous materials
US1336765A (en) Process of recovering cobalt
US1671004A (en) Process for extracting metallic nickel
US1377217A (en) Process of recovering metallic constituents from a mixture thereof
US1920442A (en) Purification of solutions of zinc salts
US1979229A (en) Removing impurities from metallurgical solutions
US2011739A (en) Process for producing cadmium
US1916302A (en) Process for the recovery of lead directly from lead ore in the form of an acetate of lead
US518732A (en) Art of producing metallic zinc
US1839800A (en) Process for the recovery of indium
US2023424A (en) Metallurgy
US2104076A (en) Lead recovery
US1283078A (en) Electrolytic recovery of zinc.