Processing of ammonium paratungstate from tungsten ores

Claim 1

The method of obtaining highly purified ammonium paratungstate crystals from tungsten ore, said method comprising: (a) reducing the ore to be processed to a very finely divided status; (b) forming a slurry of the finely divided ore in a moderately strong HCl solution and digesting the slurry at a temperature at least about 100° C for a sufficient time to substantially convert the tungsten values in the ore to WO 3 .H 2 O, separating the resulting tungstic oxide from the acid solution to remove acid-soluble impurities from said tungstic oxide, and water washing the separated tungstic oxide to remove substantially all remaining water-soluble impurities therefrom; (c) dissolving the washed tungstic oxide in an aqueous solution of Na 2 CO 3 or NaOH at a temperature slightly below the boiling point of water with the pH adjusted to a steady value of from about 8 to 8.5 to convert the insoluble tungstic oxide to soluble sodium tungstate solution, and separating the soluble sodium tungstate solution from remaining insoluble material to further remove impurities; (d) heating the resulting sodium tungstate solution to slightly below the boiling point of water and adding sodium hydroxide thereto to raise the pH to about 10.5 to 11.5, adding to said heated solution magnesium chloride in amount sufficient at least to lower the pH of said solution, thereafter adding to the resulting solution additional sodium hydroxide to raise the pH thereof to about 10.5 to 11.5 to precipitate as hydroxide the magnesium and additional metallic impurity leaving a further purified sodium tungstate solution, and separating the resulting sodium tungstate solution from the formed precipitate; (e) adding to the further purified sodium tungstate solution at least one of ammonium sulfide and thioacetamide in amount more than sufficient to react with any molybdenmum impurity present to form MoS 3 , and with the solution at a temperature slightly less than the boiling point of water acidifying the solution to a pH in the range of from about 2 to 3 to precipitate substantially all molybdenum as MoS 3 from the sodium tungstate solution, and separating the precipitated MoS 3 from the residual solution; (f) intimately contacting said purified sodium tungstate solution with a water-immiscible ion exchange liquid in which the active ingredient is amine salt the anionic portion of which is exchanged with the tungstate radical of said sodium tungstate solution to form amine tungstate and the corresponding sodium salt, settling said immiscible liquids to separate them, and isolating the separted liquids from each other; (g) intimately contacting said tungstate-containing ion exchange liquid with ammonium hydroxide solution to form immiscible ammonium tungstate solution and tungstate-stripped ion exchange liquid, settling said immiscible liquids to separate them, and isolating the separated liquids from each other; and (h) converting said isolated ammonium tungstate solution to ammonium paratungstate crystals, and separating the precipitated ammonium paratungstate crystals from residual solution.

Claim 2

The method of obtaining highly purified ammonium paratungstate crystals from tungsten ore, said method comprising: (a) reducing the ore to be processed to a very finely divided status; (b) forming a slurry of the finely divided ore in a moderately strong HCl solution and digesting the slurry at a temperature at least about 100° C for a sufficient time to substantially convert the tungsten values in the ore to WO 3 .H 2 O, separating the resulting tungstic oxide from the acid solution to remove acid-soluble impurities from said tungstic oxide, and water washing the separated tungstic oxide to remove substantially all remaining water-soluble impurities therefrom; (c) dissolving the washed tungstic oxide in an aqueous solution of Na 2 CO 3 or NaOH at a temperature slightly below the boiling point of water with the pH adjusted to a steady value of from about 8 to 8.5 to convert the insoluble tungstic oxide to soluble sodium tungstate solution, and separating the soluble sodium tungstate solution from remaining insoluble material to further remove impurities; (d) heating the resulting sodium tungstate solution to slightly below the boiling point of water and adding sodium hydroxide thereto to raise the pH to about 10.5 to 11.5, adding to said heated solution magnesium chloride in amount sufficient at least to lower the pH of said solution, thereafter adding to the resulting solution additional sodium hydroxide to raise the pH thereof to about 10.5 to 11.5 to precipitate as hydroxide the magnesium and additional metallic impurity leaving a further purified sodium tungstate solution, and separating the resulting sodium tungstate solution from the formed precipitate; (e) adding to the further purified sodium tungstate solution at least one of ammonium sulfide and thioacetamide in amount more than sufficient to react with any molybdenmum impurity present to form MoS 3 , and with the solution at a temperature slightly less than the boiling point of water acidifying the solution to a pH in the range of from about 2 to 3 to precipitate substantially all molybdenum as MoS 3 from the sodium tungstate solution, and separating the precipitated MoS 3 from the residual solution; (f) intimately contacting said purified sodium tungstate solution with a water-immiscible ion exchange liquid in which the active ingredient is amine salt the anionic portion of which is exchanged with the tungstate radical of said sodium tungstate solution to form amine tungstate and the corresponding sodium salt, settling said immiscible liquids to separate them, and isolating the separted liquids from each other; (g) intimately contacting said tungstate-containing ion exchange liquid with ammonium hydroxide solution to form immiscible ammonium tungstate solution and tungstate-stripped ion exchange liquid, settling said immiscible liquids to separate them, and isolating the separated liquids from each other; and (h) converting said isolated ammonium tungstate solution to ammonium paratungstate crystals, and separating the precipitated ammonium paratungstate crystals from residual solution.

Claim 3

The method of obtaining highly purified ammonium paratungstate crystals from tungsten ore, said method comprising: (a) reducing the ore to be processed to a very finely divided status having a particle size less than about 40 microns; (b) forming a slurry of the finely divided ore in a 17 to 26 weight percent HCl solution and digesting the slurry at a temperature from about 100° C to 140° C for from 2 to 6 hours to substantially convert the tungsten values in the ore to WO 3 .H 2 O, separating the resulting tungstic oxide from the acid solution to remove acid-soluble impurities from said tungstic oxide, and water washing the separated tungstic oxide to remove substantially all remaining water-soluble impurities therefrom; (c) dissolving the washed tungstic oxide in an aqueous solution of Na 2 CO 3 or NaOH at a temperature from about 80° to 90° C with the pH adjusted to a steady value of from about 8 to 8.5 to convert the insoluble tungstic oxide to soluble sodium tungstate solution, and separating the soluble sodium tungstate solution from remaining insoluble material to further remove impurities; (d) heating the resulting sodium tungstate solution to from about 80° to 90° C and adding sodium hydroxide thereto to raise the pH to about 10.5 to 11.5, adding to said heated solution magnesium chloride in amount sufficient at least to lower the pH of said solution, thereafter adding to the resulting solution additional sodium hydroxide to raise the pH thereof to about 10.5 to 11.5 to precipitate as hydroxide the magnesium and additional metallic impurity leaving a further purified sodium tungstate solution, and separating the resulting sodium tungstate solution from the formed precipitate; (e) adding to the further purified sodium tungstate solution at least one of ammonium sulfide and thioacetamide in amount more than sufficient to react with any molybdenum impurity present to form MoS 3 , and with the solution at a temperature from about 70° C to 95° C acidifying the solution to a pH in the range of from about 2 to 3 to precipitate substantially all molybdenum as MoS 3 from the sodium tungstate solution, and separating the precipitated MoS 3 from the residual solution; (f) intimately contacting said purified sodium tungstate solution with a water-immiscible ion exchange liquid in which the active ingredient is amine chloride the anionic portion of which is exchanged with the tungstate radical of said sodium tungstate solution to form amine tungstate and sodium chloride, settling said immiscible liquids to separate them, and isolating the separated liquids from each other; (g) intimately contacting said tungstate-containing ion exchange liquid with ammonium hydroxide solution to form immiscible ammonium tungstate solution and tungstate-stripped ion exchange liquid, settling said immiscible liquids to separate them, and isolating the separated liquids from each other; and (h) evaporating a portion of said isolated ammonium tungstate solution to evolve ammonia and to precipitate ammonium paratungstate crystals therefrom, and separating the precipitated ammonium paratungstate crystals from residual solution.

Claim 4

The method of obtaining highly purified ammonium paratungstate crystals from tungsten ore, said method comprising: (a) reducing the ore to be processed to a very finely divided status having a particle size less than about 40 microns; (b) forming a slurry of the finely divided ore in a 17 to 26 weight percent HCl solution and digesting the slurry at a temperature from about 100° C to 140° C for from 2 to 6 hours to substantially convert the tungsten values in the ore to WO 3 .H 2 O, separating the resulting tungstic oxide from the acid solution to remove acid-soluble impurities from said tungstic oxide, and water washing the separated tungstic oxide to remove substantially all remaining water-soluble impurities therefrom; (c) dissolving the washed tungstic oxide in an aqueous solution of Na 2 CO 3 or NaOH at a temperature from about 80° to 90° C with the pH adjusted to a steady value of from about 8 to 8.5 to convert the insoluble tungstic oxide to soluble sodium tungstate solution, and separating the soluble sodium tungstate solution from remaining insoluble material to further remove impurities; (d) heating the resulting sodium tungstate solution to from about 80° to 90° C and adding sodium hydroxide thereto to raise the pH to about 10.5 to 11.5, adding to said heated solution magnesium chloride in amount sufficient at least to lower the pH of said solution, thereafter adding to the resulting solution additional sodium hydroxide to raise the pH thereof to about 10.5 to 11.5 to precipitate as hydroxide the magnesium and additional metallic impurity leaving a further purified sodium tungstate solution, and separating the resulting sodium tungstate solution from the formed precipitate; (e) adding to the further purified sodium tungstate solution at least one of ammonium sulfide and thioacetamide in amount more than sufficient to react with any molybdenum impurity present to form MoS 3 , and with the solution at a temperature from about 70° C to 95° C acidifying the solution to a pH in the range of from about 2 to 3 to precipitate substantially all molybdenum as MoS 3 from the sodium tungstate solution, and separating the precipitated MoS 3 from the residual solution; (f) intimately contacting said purified sodium tungstate solution with a water-immiscible ion exchange liquid in which the active ingredient is amine chloride the anionic portion of which is exchanged with the tungstate radical of said sodium tungstate solution to form amine tungstate and sodium chloride, settling said immiscible liquids to separate them, and isolating the separated liquids from each other; (g) intimately contacting said tungstate-containing ion exchange liquid with ammonium hydroxide solution to form immiscible ammonium tungstate solution and tungstate-stripped ion exchange liquid, settling said immiscible liquids to separate them, and isolating the separated liquids from each other; and (h) evaporating a portion of said isolated ammonium tungstate solution to evolve ammonia and to precipitate ammonium paratungstate crystals therefrom, and separating the precipitated ammonium paratungstate crystals from residual solution.