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US3969484A Expired / Lapsed US ⏱️ 0.0 years remaining

Process for recovering tungsten from alkaline leaching solution of tungsten ores

Assignee: Nittetsu Mining Co Ltd
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Filing: 1975-02-20
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Granted: 1976-07-13
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Expires: 1995-02-20
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Abstract

Abstract This invention relates to a process for recovering tungsten from an alkaline leaching solution of tungsten ores. This invention comprises adjusting the pH of an alkaline leaching solution which is obtained by lixiviating ore containing tungsten with an alkaline solution to 7-8 with acid to oxidize molybdic acid ions in the solution, adding a sulfide donor, then precipitating molybdenum sulfide compounds by adjusting the pH value of the solution to 2-3, and recovering tungstic acid ions as calcium tungstate by the addition of a calcium ion donor after the molybdenum sulfide compounds are separated.

Inventors

  • 👤 Satoshi Onozaki
  • 👤 Shogo Nemoto
  • 👤 Takeshi Hazeyama

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-04 18:48
CPC Classifications
C; C22; C22B; C22B34/00; C22B34/30; C22B34/36; C01; C01G; C01G41/00

Claims Analysis

Total Claims: 6
Claim 1
Independent Claim 230 words
A process for recovering tungsten values from an alkaline solution employed in the leaching of tungsten ores containing molybdenum, which comprises: adjusting the pH of said alkaline leaching solution containing tungsten and molybdenum values to a range of 7- 8 with a mineral acid which does not form a precipitate with calcium ions, whereby the molybdenum values and tungsten values exist as molybdic acid and tungstic acid, respectively; oxidizing said molydbic acid ions in solution; adding at least twice the stoichiometric amount with respect to said molybdic acid of at least one sulfide ion donor selected from the group consisting of hydrogen sulfide, alkali sulfides and alkali hydrosulfide to said molydbic acid containing solution at a temperature of 30°-80°C whereby molybdic acid ions are converted to complex thiomolybdate ions; adjusting the pH of said sulfide ion treated solution to 2-3 with a mineral acid which does not form a precipitate with calcium ions; separating the molybdenum sulfide compounds upon cooling which precipitate from pH adjusted solution; oxidizing said tungstic acid in the molybdenum free solution; adding at least one calcium ion donor selected from the group consisting of calcium chloride and calcium hydroxide to said tungstic acid containing solution at 30°-80°C which converts tungstic acid ions to calcium tungstate; and cooling said calcium tungstate containing solution to precipitate said calcium tungstate from solution which thereafter is separated from the solution.
Claim 2
Dependent Claim 230 words
A process for recovering tungsten values from an alkaline solution employed in the leaching of tungsten ores containing molybdenum, which comprises: adjusting the pH of said alkaline leaching solution containing tungsten and molybdenum values to a range of 7- 8 with a mineral acid which does not form a precipitate with calcium ions, whereby the molybdenum values and tungsten values exist as molybdic acid and tungstic acid, respectively; oxidizing said molydbic acid ions in solution; adding at least twice the stoichiometric amount with respect to said molybdic acid of at least one sulfide ion donor selected from the group consisting of hydrogen sulfide, alkali sulfides and alkali hydrosulfide to said molydbic acid containing solution at a temperature of 30°-80°C whereby molybdic acid ions are converted to complex thiomolybdate ions; adjusting the pH of said sulfide ion treated solution to 2-3 with a mineral acid which does not form a precipitate with calcium ions; separating the molybdenum sulfide compounds upon cooling which precipitate from pH adjusted solution; oxidizing said tungstic acid in the molybdenum free solution; adding at least one calcium ion donor selected from the group consisting of calcium chloride and calcium hydroxide to said tungstic acid containing solution at 30°-80°C which converts tungstic acid ions to calcium tungstate; and cooling said calcium tungstate containing solution to precipitate said calcium tungstate from solution which thereafter is separated from the solution.
Claim 3
Dependent Claim 21 words
The process of claim 1, wherein the ores are leached with soda ash solution at high temperatures and under high pressures.
Claim 4
Dependent Claim 43 words
The process of claim 1, wherein the pH of said solution to which said calcium compound is added, is adjusted to less than 10 by hydrochloric acid or nitric acid, and then calcium tungstate is separated from the solution after it is cooled.
Claim 5
Dependent Claim 35 words
The process of claim 1, wherein the amount of said calcium compound added to said tungstic acid containing solution is in excess of the stoichiometric amount necessary to convert the tungstic ion to calcium tungstate.
Claim 6
Dependent Claim 34 words
The process of claim 1, wherein the oxidizing agent used in both oxidation steps is selected from the group consisting of air, ozone, oxygen, chlorine, hydrogen peroxide, bleaching powder, alkali chlorate and alkali nitrite.

References Cited (Backward Citations)

US2339888A Cited
US2556255A Cited
US3158438A Cited
US3173754A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1979-07-13 1980-01-12 1980-07-13 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1983-07-13 1984-01-12 1984-07-13 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1987-07-13 1988-01-12 1988-07-13 $7700.00 Window Closed / Lapsed

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