Chevron U.s.a. Inc.

Sherritt International Corporation

Eldorado Gold Corporation

Roman Berezowsky

John Stiksma

Rahul Shankar Bhaduri

Jinxing Ji

Paul Skayman

A process for reducing arsenic content from arsenic-bearing gold concentrate or other arsenic-bearing gold materials to produce a low arsenic-bearing gold concentrate. The process may comprise adding oxygen, water, and/or acid to an acidulated arsenic-bearing gold concentrate slurry and reacting them together in an autoclave at an elevated pressure and temperature in a pressure oxidation step. In one or more examples, the process may further comprise processing the oxidized concentrate slurry in an arsenic re-dissolution step to dissolve unstable solid arsenic compounds, and applying a first solid/liquid separation and wash step to form a first washed slurry/solid and first acid-containing solutions. The process may further comprise reacting the first washed slurry/solid with sulfur dioxide in a reductive leach step, and applying a second solid/liquid separation and wash step to form a second washed slurry/solid and second acid-containing solutions. The second washed slurry/solid may be a low arsenic-bearing gold concentrate.

Method for reducing arsenic content in arsenic-bearing gold material

Methods for recovering base metals, including, among other metals, molybdenum and nickel, from metal sulfides containing a Group VIB metal and a Group VIII metal. Generally, the methods comprise: contacting metal sulfides with a leaching solution containing ammonia and air to dissolve the metals into the leaching solution, forming a slurry containing soluble complexes of the metals, ammonium sulphate and solid residue containing ammonium metavanadate and any carbonaceous materials. The solid residue containing ammonium metavanadate and carbonaceous materials is then separated from the slurry and metal complexes are precipitated from the slurry by adjusting the pH. A second slurry may be formed comprising a second solid residue and a primary filtrate comprising ammonium sulfate solution that is substantially free of metals. The second solid residue is separated from the primary filtrate comprising ammonium sulfate by any means suitable for separation of solids from liquids and is then dissolved, at a second pre-selected pH, to form a Group VIB metal precipitate and a Group VIII metal containing solution. Group VIB and Group VIII metals can be easily recovered from the precipitate and solution, respectively. In some embodiments Group VB metals are recovered as well.

Recovering metals from complex metal sulfides

A method is disclosed for separating and recovering base metals from a used hydroprocessing catalyst originating from Group VIB and Group VIII metals and containing at least a Group VB metal. In one embodiment, the used catalyst is contacted with an ammonia leaching solution to dissolve and separate the Group VIB and VIII metals from the Group VB metal complex and coke associated with the used catalyst. The resulting Group VIB and VIII metal containing solution is processed through at least two additional precipitation and liquid/solid separation steps to produce, in separate processing streams, a Group VIB metal product solution (such as ammonium molybdate) and a Group VIII metal product solution (such as nickel sulfate). Additionally, two separate filtrate streams are generated from liquid-solid separation steps, which filtrate streams are combined and subjected to hydrolysis and oxidation (oxydrolysis) to generate a purified ammonium sulfate solution for further processing, such as for fertilizer.

Process for separating and recovering base metals from used hydroprocessing catalyst

A method is disclosed for separating and recovering base metals from a used hydroprocessing catalyst originating from Group VIB and Group VIII metals and containing at least a Group VB metal. In one embodiment, the method comprises the steps of: contacting the used catalyst with an ammonia leaching solution under conditions sufficient to dissolve the group VIB metal and the Group VIII metal into the leaching solution; forming a leached slurry containing at least a group VIB metal complex and at least a group VIII metal complex, ammonium sulfate and a solid residue containing at least a Group VB metal complex and coke; separating and removing from the leached slurry the solid residue and coke; precipitating from the remaining solution at least a portion of the Group VIB metal complex and at least a portion of the Group VIII metal complex by controlling the pH to form a liquid material substantially free of Group VB, Group VIB and Group VIII metals and another solid material comprising substantially Group VIB and Group VIII metal complexes. Said solid material is further processed by dissolution, means of separation, further means of precipitation and oxidative dissolution to produce, separately, a Group VIB metal product solution, a Group VIII metal product solution and a purified ammonium sulfate product solution.

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St. Albert, Canada

Roman Berezowsky