A method for vitrification of arsenic and antimony, comprising substituting oxygen to sulfur on thiosalts, incorporating resulting sodium arsenate and sodium antimonate into a sodium silicate glass-forming mixture and vitrifying the sodium silicate glass-forming mixture into a resulting glass sequestering the arsenic and antimony.

A stabilization process for an arsenic solution comprising thiosulfates, the process comprising: acidifying the arsenic solution to decompose the thiosulfates, to yield an acidified solution; oxidizing the acidified solution to oxidize residual As.sup.3+ to As.sup.5+ and reduced sulfur species to sulfates, to yield a slurry comprising elemental sulfur; separating elemental sulfur from the slurry to yield a liquid; oxidizing the liquid to oxidize residual reduced sulfur species, to yield an oxidized solution; and forming a stable arsenic compound from the oxidized solution.

A stabilization process for an arsenic solution comprising thiosulfates, the process comprising: acidifying the arsenic solution to decompose the thiosulfates, to yield an acidified solution; oxidizing the acidified solution to oxidize residual As.sup.3+ to As.sup.5+ and reduced sulfur species to sulfates, to yield a slurry comprising elemental sulfur; separating elemental sulfur from the slurry to yield a liquid; oxidizing the liquid to oxidize residual reduced sulfur species, to yield an oxidized solution; and forming a stable arsenic compound from the oxidized solution.

A process is provided for separation of at least one metal sulfide from a mixed sulfide concentrate. The process includes: subjecting the mixed sulfide concentrate to flotation in which at least one sulfide including antimony, arsenic and a first metal is floated and at least one sulfide including a second metal is depressed. The flotation yields a first metal concentrate having the at least one sulfide including antimony, arsenic and the first metal and a second metal concentrate having the at least one sulfide including the second metal. The first metal concentrate is leached to yield a further concentrate and a leach solution. The further concentrate includes the first metal and the leach solution includes soluble antimony and soluble arsenic. The process further includes oxidizing the leach solution to yield an antimony precipitate and an arsenic solution, and forming a stable arsenic compound from the arsenic solution.

A process is provided for separation of at least one metal sulfide from a mixed sulfide concentrate. The process includes: subjecting the mixed sulfide concentrate to flotation in which at least one sulfide including antimony, arsenic and a first metal is floated and at least one sulfide including a second metal is depressed. The flotation yields a first metal concentrate having the at least one sulfide including antimony, arsenic and the first metal and a second metal concentrate having the at least one sulfide including the second metal. The first metal concentrate is leached to yield a further concentrate and a leach solution. The further concentrate includes the first metal and the leach solution includes soluble antimony and soluble arsenic. The process further includes oxidizing the leach solution to yield an antimony precipitate and an arsenic solution, and forming a stable arsenic compound from the arsenic solution.

A method for vitrification of arsenic and antimony, comprising substituting oxygen to sulfur on thiosalts, incorporating resulting sodium arsenate and sodium antimonate into a sodium silicate glass-forming mixture and vitrifying the sodium silicate glass-forming mixture into a resulting glass sequestering the arsenic and antimony.

The method and the device serve to treat the flue dust formed during the production of nonferrous metals. After the addition of sulfur and/or a sulfur compound, the flue dust is heated, and volatile compounds are separated in a downstream offgas treatment unit. The flue dust is heated in an inert atmosphere.

The method and the device serve to treat the flue dust formed during the production of nonferrous metals. After the addition of sulfur and/or a sulfur compound, the flue dust is heated, and volatile compounds are separated in a downstream offgas treatment unit. The flue dust is heated in an inert atmosphere.

A hydrometallurgical process for the removal of arsenic and antimony from a so-called dirty copper concentrate (101) is described. The process comprises the following steps: Step 1: repulping (100) the dirty copper concentrate with an alkaline lixiviant (102, 103), and subjecting the dirty copper concentrate to an alkaline leaching process (the Leach) in a Leach reactor (110). The arsenic and antimony are dissolved in the Leach to produce a clean copper concentrate (138) and leach discharge liquor (132). Step 2: subjecting the Leach discharge liquor (132) to a lime treatment step (151) in order to regenerate (150) the alkaline lixiviant as well as precipitate an impurity rich precipitate (161) containing arsenic and antimony. Then the impurity rich precipitate (161) is separated (160) from the regenerated alkaline lixiviant (162). The impurity rich precipitate is washed and disposed of in an environmentally safe condition. Step 3: recycling the regenerated alkaline lixiviant (162) to the Leach in Step 1, and so employing the recycled alkaline lixiviant (102) in the further extraction of arsenic and antimony from incoming dirty copper concentrate (101).

A hydrometallurgical process for the removal of arsenic and antimony from a so-called dirty copper concentrate (101) is described. The process comprises the following steps: Step 1: repulping (100) the dirty copper concentrate with an alkaline lixiviant (102, 103), and subjecting the dirty copper concentrate to an alkaline leaching process (the Leach) in a Leach reactor (110). The arsenic and antimony are dissolved in the Leach to produce a clean copper concentrate (138) and leach discharge liquor (132). Step 2: subjecting the Leach discharge liquor (132) to a lime treatment step (151) in order to regenerate (150) the alkaline lixiviant as well as precipitate an impurity rich precipitate (161) containing arsenic and antimony. Then the impurity rich precipitate (161) is separated (160) from the regenerated alkaline lixiviant (162). The impurity rich precipitate is washed and disposed of in an environmentally safe condition. Step 3: recycling the regenerated alkaline lixiviant (162) to the Leach in Step 1, and so employing the recycled alkaline lixiviant (102) in the further extraction of arsenic and antimony from incoming dirty copper concentrate (101).