The patent badge is an abbreviated version of the USPTO patent document. The patent badge does contain a link to the full patent document.

The patent badge is an abbreviated version of the USPTO patent document. The patent badge covers the following: Patent number, Date patent was issued, Date patent was filed, Title of the patent, Applicant, Inventor, Assignee, Attorney firm, Primary examiner, Assistant examiner, CPCs, and Abstract. The patent badge does contain a link to the full patent document (in Adobe Acrobat format, aka pdf). To download or print any patent click here.

Date of Patent:
Jul. 14, 1981

Filed:

Apr. 15, 1980
Applicant:
Inventors:

Alkis S Rappas, Bedford, MA (US);

Jameel Menashi, Lexington, MA (US);

Donald A Douglas, Amherst, NH (US);

Assignee:

Cabot Corporation, Kokomo, IN (US);

Attorneys:
Primary Examiner:
Int. Cl.
CPC ...
C01G / ; C01G / ;
U.S. Cl.
CPC ...
423 58 ; 7510 / ; 423 55 ; 423 53 ; 423166 ; 423 57 ; 423 62 ; 423 68 ;
Abstract

Disclosed is a process for recovering chromium, vanadium, molybdenum, and tungsten from secondary resources such as alloy scrap comprising a refractory metal and base metals such as cobalt, nickel, iron, and copper. The scrap is calcined with sodium carbonate in air to convert the refractory metal values to MoO.sub.4.sup..dbd., VO.sub.4.sup..tbd., WO.sub.4.sup..dbd., and CrO.sub.4.sup..dbd. and the base metals to water insoluble oxides. A leach of the calcined materials produces a pregnant liquor rich in refractory metals which, after separation of the vanadium, molybdenum and tungsten values, is treated with CO, CHOO.sup.-, CH.sub.3 OH, or HCHO to reduce Cr.sup.+6 to Cr.sup.+3. The carbonate and bicarbonate salts produced as a byproduct of the reduction are recycled to the calcination stage. As a result of the V, W, and Mo partition, a mixed solid comprising CaO.nV.sub.2 O.sub.5, CaMoO.sub.4, and CaWO.sub.4 is produced. This is treated with carbonated water or formic acid to selectively dissolve vanadium values which are subsequently recovered by precipitation or extraction. The remaining mixed CaWO.sub.4 and CaMoO.sub.4 solid is treated with H.sub.2 O.sub.2 and sulfuric acid to reject a Mo and W-free CaSO.sub.4 precipitate, and to produce a concentrated solution of tungsten and molybdenum. The W values are selectively precipitated from this solution by decomposing the peroxy complexes. The process has the advantages that a wide variety of different feed materials can be treated, no energy intensive pyrometallurgy is involved, reagent consumption is minimized, and no aqueous effluents are produced.


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