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Production of pure molybdenum oxide from low grade molybdenite concentrates

A technology of molybdenite and concentrate, applied in the field of producing pure molybdenum oxide from low-grade molybdenite concentrate

Inactive Publication Date: 2008-09-03
H C STARCK GMBH
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Also, amines are relatively nonselective and may transfer silicon, phosphorus, and arsenic as heteropoly compounds

Method used

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  • Production of pure molybdenum oxide from low grade molybdenite concentrates
  • Production of pure molybdenum oxide from low grade molybdenite concentrates
  • Production of pure molybdenum oxide from low grade molybdenite concentrates

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Experimental program
Comparison scheme
Effect test

Embodiment 1

[0068] displacement precipitation process

[0069] After pressure oxidation of the molybdenite concentrate and solid-liquid separation of the slurry in an autoclave, the resulting acidic liquid is subjected to displacement precipitation. The main components of the liquid are approximately:

[0070] Mo, g / l

10-16

Cu, g / l

8-11

Fe, g / l

8-11

h 2 SO 4 , g / l

100

[0071] The displacement precipitation process was carried out at room temperature. At the beginning, each gram of iron (Fe 3+ ) Add iron to the liquid at a ratio of 1 gram of iron to 2 grams of iron for every 1 gram of copper in the liquid. The slurry was mixed for 10-15 minutes, then filtered. The solid contained recovered Cu species. The filtrate is then processed to recover Mo.

[0072] By adding Na 2 CO 3 Or NaOH to increase the pH of the filtrate to about 1.05-1.2, and the temperature of the filtrate to about 40-65°C. Then add iron according to ...

Embodiment 2

[0079] Alkaline extraction

[0080] Several experiments were carried out in an attempt to optimize the leaching conditions while minimizing bicarbonate formation. Alkaline extraction data are listed in Table 3. Leaching with sodium carbonate at pH below 7.0 showed almost complete dissolution of molybdenum, but co-dissolution of iron was also significant, probably as carbonate complexes. Leaching with sodium hydroxide did not dissolve much iron. Therefore, trials to optimize the cost and efficiency of leaching evaluated leaching with sodium carbonate starting at pH 6 followed by leaching at pH 9 with sodium hydroxide or leaching with sodium hydroxide alone. Molybdenum was extracted in excess of 98% in these tests (see Table 3, extraction numbers CL-1-CL-6). The leach solution contained 43-79 g / l Mo with silicon being the only significant impurity. Reagent requirements are, on average, about 1.1 lbs of Na per lb of dissolved molybdenum 2 CO 3 and 0.7 lbs NaOH.

Embodiment 3

[0082] alkaline leaching solvent extraction

[0083] Several experiments were carried out to determine the optimum conditions for solvent extraction of molybdenum from alkaline leaching solutions. Solvent extraction studies of molybdenum employed organics containing 10% tridecylamine, 5% decanol and 85% Escaid 110. The results of these studies are summarized in Tables 4A-4C. Initial experiments evaluated the effect of temperature in the pH range of 2.0-2.7. Temperature had no significant effect on molybdenum extraction. For feed solutions containing 63-70 g / l molybdenum, the raffinate contained only 1-40 mg / l molybdenum (>99.9% transfer), indicating a very efficient extraction. The partition coefficient in the freshly stripped organic phase and the feed in the first contact was as high as 133 (g / l Mo organic phase÷g / l Mo aqueous phase). Some silicon and arsenic transfer occurred. When corrected to 200 g / l molybdenum, the first stripping stage contained up to 310 mg / l sili...

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Abstract

Disclosed is a method of high purity ammonium dimolybdate produced by the pressure oxidation of low grade molybdenite concentrates. The method includes (a) forming the low grade molybdenite concentrates into the aqueous serosity; (b) oxidating the serosity in the ambience containing the free phenol under the pressure 50 p.s.i. and the temperature under 200 DEG C to generate the first drainage; (c) leaching the first drainage using the aqueous alkali to generate the second drainage; (d) separating and filtering the second drainage to generate the filtrate containing the soluble molybdenum and a solid filter cake containing the unsoluable molybdenum; (e) performing the solvent extraction using the organic solvent, reclaiming the molybdenum from the fluid filtrate, leaching the organic phase by the ammonium hydroxide to generate the first mother liquor; (f) crystallizing the first mother liquor containing the leached molybdenum to generate the crystallization and the second mother liquor; (g) reclaiming the high purity ammonium dimolybdate from the crystallization.

Description

[0001] The patent application of the present invention is a Chinese patent application filed on September 1, 2001 with the international application number PCT / US01 / 30067, the national application number 01823236.1, and the invention title "Production of pure molybdenum oxide from low-grade molybdenite concentrate" divisional application. technical field [0002] This invention relates to a process for the production of ammonium dimolybdenite from molybdenite concentrate for conversion into pure molybdenum oxide or other pure chemicals, and more particularly to the process of oxidation of low grade molybdenite concentrate by pressure Process for preparing chemical grade ammonium dimolybdate for conversion to chemical grade molybdenum oxide. Background technique [0003] The extraction of molybdenum from molybdenite-bearing materials by aqueous methods has been the subject of research for almost 50 years. In 1952, E.S. Usataya 1 The oxidation reaction of molybdenite in aque...

Claims

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Application Information

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IPC IPC(8): C01G39/00C01G39/02B01D9/02B01D11/00B01D11/02B01D11/04C22B3/44C22B15/00C22B34/34
CPCC01G39/003C01G39/02C01G39/00
Inventor R·W·巴里特W·库马J·E·里兹L·F·麦克休H·H·K·诺塔P·B·奎诺R·-C·吴
Owner H C STARCK GMBH