Liquid-liquid extraction of germanium from aqueous solution using hydroxy-oximes

Information

  • Patent Grant
  • RE33410
  • Patent Number
    RE33,410
  • Date Filed
    Monday, February 26, 1990
    35 years ago
  • Date Issued
    Tuesday, October 30, 1990
    34 years ago
Abstract
Process for extraction of germanium from aqueous acid solution by contacting with an organic liquid containing a hydroxy-oxime and recovering the extracted germanium from the organic phase.
Description

Certain germanium containing Cu/Pb/Zn sulfide concentrates are processed by subjecting them to a selective roasting during which the germanium is oxidized at the same time as a part of the metals Zn, Fe and Cu. After lixiviation of the roast a sulfuric solution is obtained with a low germanium content. Impure Ge solutions are also obtained from residues of manufacture and from other by-products.
Known methods for concentrating Ge from impure solutions consist in precipitating the Ge as tannate, sulfide or mixed hydroxides. The precipitates are subjected to treatments which end with the distillation of the GeCl.sub.4.
The present invention describes a process for separating Ge by liquid-liquid extraction from various acid solution.
It has now been found that Ge may be selectively extracted from acid solutions by means of a hydroxy-oxime and that the extraction capacity of such extractant increases with the acidity.
It is known that organic products containing a hydroxy-oxime can selectively extract copper at a very low acidity, while their extracting power for copper is strongly diminished when the acidity increases.
The selectivity of the Ge extraction, compared to that of the copper, may thus be increased by choosing an appropriate acidity of the solution.
The extractant is also very selective with regard to other metallic ions (only trivalent iron is partially extracted at the same time).
Germanium is extracted from aqueous acid solutions containing metallic or non metallic impurities, by bringing said solution in contact, co-current or counter-currentwise, repeatedly or not, with an organic liquid containing a hydroxy-oxime.
The aqueous solution may contain besides germanium also 10 to 500 g/liter of sulfuric acid or hydrochloric acid, or 10 to 100 g/liter of hydrofluoric acid, as well as other metallic or non-metallic ions at different concentrations.
The organic liquid may consist of hydroxy-oxime, or of a solution of a hydroxy-oxime in an aliphatic solvent and/or an aromatic solvent, and possibly a higher alcohol. The organic liquid will preferelly contain at least 1% by volume of a hydroxy-oxime and up to 10% by volume of a higher alcohol.
.[.It has been found that.]. 19-hydroxyhexatriaconta-9,28diene-18 oxime, .Iadd.an .alpha.-hydroxy-oxime, may be used. It has been found that 5,8-diethyl-hydroxydodecan-6-oxime, an .alpha.-hydroxy-oxime, .Iaddend.sold under the registered name of LIX-63 (made by "General Mills Inc." Tuscon, U.S.A.) is particularly well suited for the extraction of germanium.
It has been noted that aliphatic products, such as kerosene, are well suited as organic solvents for hydroxy-oxime.
A higher alcohol which may advantageously be used is isodecanol.
Examples given below show that the simultaneous extraction of Cu is low. However, copper may previously be eliminated, either by selective cementation in acid medium, or by previous selective extraction, or by any other known method entailing no loss of Ge.
The invention also covers the re-extraction of the Ge from the organic solution by means of water or an acid or alkaline solution. Direct precipitation of the germanium in the organic solution is also possible.
The precipitation may be obtained by adding a gaseous base such as NH.sub.3, or a solid base such as lime- or magnesia wash, or a liquid base such as a NaOH or a KOH solution.
After re-extraction of the germanium, the organic solution may be used again for another extraction.
When the starting solutions contain Cu, the latter may be re-extracted after the Ge, by means of an acid solution such as a sulfuric acid solution.
It is thus possible to control the separation selectivity of Ge and Cu by a suitable choice of the operating conditions for the extraction and for the reextraction.





EXAMPLE 1
______________________________________Aqueous solution: Ge 5 g/l As 2.68 g/l Zn 4.60 g/l Ni 0.020 g/l Cu 6.79 g/l Fe.sup.III 3 g/l Fe.sub.tot 59.82 g/l Cl 0.130 g/l H.sub.2 SO.sub.4 157 g/lExtraction.Organic solution: LIX 63 diluted at 50% with kerosene. ##STR1##Number of extraction stages: 7Raffinate obtained after extraction:Ge 0.019 g/lAs 2.68 g/lZn 4.60 g/lNi 0.02 g/lCu 6.39 g/lFe.sup.III 1.5 g/lFe.sub.tot 58.3 g/lCl 0.130 g/lH.sub.2 SO.sub.4 157 g/lYield of Ge extraction: 99.968%.2-stage elution1st stage:Elution solution: NaOH 175 g/l ##STR2##Number of elution stages: 6Germanium-containing eluate: Ge: 98 g/l Cu: traces Fe: 0.45 g/l NaOH: 67 g/lelution efficiency of Ge: 99%.2nd stage:Elution solution: H.sub.2 SO.sub.4 200 g/l ##STR3##Number of elution stages: 2Eluate obtained after elution: Ge: traces Cu: 16 g/l______________________________________
EXAMPLE 2
______________________________________Aqueous solution: Ge 3.5 g/l Cu 0.0008 g/l Zn 2.5 g/l Ni 0.008 g/l As 0.79 g/l Fe.sub.tot 45 g/l Fe.sup.III 1.5 g/l H.sub.2 SO.sub.4 460 g/lExtractionOrganic solution: LIX-63 diluted at 30% with kerosene. ##STR4##Number of extraction states: 7Raffinate obtained after extraction:Ge 0.007 g/lCu 0.0008 g/lZn 2.5 g/lNi 0.008 g/lAs 0.79 g/lFe.sup.III 0.5 g/lFe.sub.tot 44 g/lH.sub.2 SO.sub.4 460 g/lYield of Ge extraction: 99.98%.______________________________________
EXAMPLE 3
______________________________________Aqueous solution: Ge 5 g/l Cu 0.0008 g/l Zn 2.5 g/l Ni 0.008 g/l As 0.54 g/l Fe.sub.tot 69 g/l Fe.sup.III 1.3 g/l H.sub.2 SO.sub.4 130 g/lExtractionOrganic solution: LIX-63 100% ##STR5##Number of extraction stages: 4Raffinate obtained after extraction:Ge 0.002 g/lCu 0.0008 g/lZn 2.47 g/lNi 0.008 g/lAs 0.48 g/lFe.sub.tot 67.3 g/lFe.sup.III tracesH.sub.2 SO.sub.4 130 g/lYield of Ge extraction: 99.99%.______________________________________
Claims
  • 1. A process for liquid-liquid extraction of germanium from an aqueous solution, in which an organic liquid containing .[.hydroxy-oxime.]. .Iadd..alpha.-hydroxy-oxime .Iaddend.is used as extractant comprising contacting an aqueous solution containing germanium and an acid selected from the group consisting of 10 to 500 grams per liter of hydrochloric acid, 10 to 500 grams per liter of sulfuric acid, and 10 to 100 grams per liter of hydrofluoric acid, with an organic liquid selected from the group consisting of non-diluted .[.hydroxy-oxime.]. .Iadd..alpha.-hydroxy-oxime.Iaddend., a solution of .[.hydroxy-oxime.]. .Iadd..alpha.-hydroxy-oxime .Iaddend.in an aliphatic solvent, a solution of .[.hydroxy-oxime.]. .Iadd..alpha.-hydroxy-oxime .Iaddend.in an aromatic solvent, and a solution of .[.hydroxy-oxime.]. .Iadd..alpha.-hydroxy-oxime .Iaddend.in a mixture of an aliphatic and an aromatic solvent, separating the organic liquid phase containing extracted germanium from the residual aqueous phase, and recovering the extracted germanium from the separated organic phase by contacting with an agent selected from the group consisting of water, acids, and bases.
  • 2. A process as claimed in claim 1, in which the aqueous solution contains 10 to 500 g/l of an acid chosen in the class consisting of sulfuric acid and hydrochloric acid.
  • 3. A process as claimed in claim 1, in which the aqueous solution contains 10 to 100 g/l hydrofluoric acid.
  • 4. A process as claimed in claim 1, in which a non-diluted hydroxy-oxime is used as the organic liquid.
  • 5. A process as claimed in claim 1, in which a solution of a hydroxy-oxime in an aliphatic solvent is used as the organic liquid.
  • 6. A process as claimed in claim 1, in which a solution of a hydroxy-oxime in an aromatic solvent is used as the organic liquid.
  • 7. A process as claimed in claim 5, in which a higher alcohol is added to the hydroxy-oxime solution.
  • 8. A process as claimed in claim 5, in which the organic liquid contains at least 1% by volume of a hydroxy-oxime.
  • 9. A process as claimed in claim 6, in which the organic liquid contains up to 10% by volume of a higher alcohol.
  • 10. A process as claimed in claim 1, in which 19-hydroxyhexatriaconta-9,28 diene-18-oxime is used as hydroxy-oxime.
  • 11. A process as claimed in claim 5, in which kerosene is used as the solvent.
  • 12. A process as claimed in claim 7, in which isodecanol is used as the higher alcohol.
  • 13. A process as claimed in claim 1, in which the separated organic phase is regenerated by contacting it with a base, and is used again for another extraction.
  • 14. A process as claimed in claim 13, in which use is made as a base of an aqueous solution of a compound selected from the group consisting of NaOH, KOH, limewash, magnesiawash, and ammonia.
  • 15. A process as claimed in claim 1, in which the aqueous solution contains copper.
  • 16. A process as claimed in claim 15, in which the separated organic phase is regenerated first by contacting it with a base in order to separate the germanium, and afterwards with an acid solution in order to separate the copper, and is used again for another extraction. .Iadd.
  • 17. A process as claimed in claim 1, in which 5,8-diethyl-7-hydroxydodecan-6-oxime is used as the .alpha.-hydroxy-oxime.
Priority Claims (1)
Number Date Country Kind
67596 May 1973 BEX
US Referenced Citations (4)
Number Name Date Kind
3276863 Drobnick et al. Oct 1966
3284501 Swanson Nov 1966
3455680 Ashbrook et al. Jul 1969
3903236 McCutcheon et al. Sep 1975
Foreign Referenced Citations (2)
Number Date Country
2125095 May 1971 DEX
1322532 Jul 1973 GBX
Non-Patent Literature Citations (3)
Entry
Smithson, Jr. et al., Journal of Metals, Sep. 1966, pp. 1037-1046.
Habashi, Fathi, Extractive Metallurgy, vol. 2, Gordon and Breach, Science Publishers, Paris 1970, p. 339.
Atwood, R. L. and Miller, J. D., Structure and Composition of Commercial Copper Chelate Extractants, preprint paper presented at The Annual Meeting of the American Institute of Mining, Metallurgical and Petoleum Engineers, San Francisco, Calif., on Feb. 20-24, 1972.
Reissues (1)
Number Date Country
Parent 464387 Apr 1974