US20150122667A1 - Method of leaching molybdenum from sulfide mineral containing molybdenum and copper through electrolytic oxidation scheme - Google Patents
Method of leaching molybdenum from sulfide mineral containing molybdenum and copper through electrolytic oxidation scheme Download PDFInfo
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- US20150122667A1 US20150122667A1 US14/091,148 US201314091148A US2015122667A1 US 20150122667 A1 US20150122667 A1 US 20150122667A1 US 201314091148 A US201314091148 A US 201314091148A US 2015122667 A1 US2015122667 A1 US 2015122667A1
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- molybdenum
- leaching
- sulfide mineral
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- mineral containing
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- 238000002386 leaching Methods 0.000 title claims abstract description 87
- 239000010949 copper Substances 0.000 title claims abstract description 75
- 229910052750 molybdenum Inorganic materials 0.000 title claims abstract description 74
- 238000000034 method Methods 0.000 title claims abstract description 56
- 229910052569 sulfide mineral Inorganic materials 0.000 title claims abstract description 54
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 title claims abstract description 53
- 239000011733 molybdenum Substances 0.000 title claims abstract description 53
- 229910052802 copper Inorganic materials 0.000 title claims abstract description 46
- 238000007254 oxidation reaction Methods 0.000 title claims abstract description 43
- 230000003647 oxidation Effects 0.000 title claims abstract description 42
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 title claims abstract description 24
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 claims abstract description 16
- 238000007598 dipping method Methods 0.000 claims abstract description 7
- HTXDPTMKBJXEOW-UHFFFAOYSA-N dioxoiridium Chemical compound O=[Ir]=O HTXDPTMKBJXEOW-UHFFFAOYSA-N 0.000 claims description 24
- CWQXQMHSOZUFJS-UHFFFAOYSA-N molybdenum disulfide Chemical compound S=[Mo]=S CWQXQMHSOZUFJS-UHFFFAOYSA-N 0.000 claims description 22
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 claims description 21
- 229910052982 molybdenum disulfide Inorganic materials 0.000 claims description 19
- 239000010931 gold Substances 0.000 claims description 12
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 claims description 10
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims description 9
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 7
- 229910052697 platinum Inorganic materials 0.000 claims description 7
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 claims description 6
- 229910052737 gold Inorganic materials 0.000 claims description 6
- 239000010936 titanium Substances 0.000 claims description 6
- 239000011780 sodium chloride Substances 0.000 claims description 5
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 4
- 229910021397 glassy carbon Inorganic materials 0.000 claims description 4
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 claims description 3
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 claims description 3
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 claims description 3
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims description 3
- 229910017052 cobalt Inorganic materials 0.000 claims description 3
- 239000010941 cobalt Substances 0.000 claims description 3
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 claims description 3
- 239000010439 graphite Substances 0.000 claims description 3
- 229910002804 graphite Inorganic materials 0.000 claims description 3
- 229910052759 nickel Inorganic materials 0.000 claims description 3
- VSZWPYCFIRKVQL-UHFFFAOYSA-N selanylidenegallium;selenium Chemical compound [Se].[Se]=[Ga].[Se]=[Ga] VSZWPYCFIRKVQL-UHFFFAOYSA-N 0.000 claims description 3
- 229910052709 silver Inorganic materials 0.000 claims description 3
- 239000004332 silver Substances 0.000 claims description 3
- 229910001220 stainless steel Inorganic materials 0.000 claims description 3
- 239000010935 stainless steel Substances 0.000 claims description 3
- 229910052719 titanium Inorganic materials 0.000 claims description 3
- 238000006243 chemical reaction Methods 0.000 description 13
- 239000012141 concentrate Substances 0.000 description 12
- 230000003247 decreasing effect Effects 0.000 description 9
- 230000008569 process Effects 0.000 description 9
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 5
- 238000004458 analytical method Methods 0.000 description 5
- 239000003795 chemical substances by application Substances 0.000 description 4
- 229910052751 metal Inorganic materials 0.000 description 4
- 239000002184 metal Substances 0.000 description 4
- 229910000476 molybdenum oxide Inorganic materials 0.000 description 4
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 230000008901 benefit Effects 0.000 description 3
- 150000002500 ions Chemical class 0.000 description 3
- 229910052742 iron Inorganic materials 0.000 description 3
- 230000001678 irradiating effect Effects 0.000 description 3
- 238000012986 modification Methods 0.000 description 3
- 230000004048 modification Effects 0.000 description 3
- 230000001590 oxidative effect Effects 0.000 description 3
- 230000035484 reaction time Effects 0.000 description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- 229910015667 MoO4 Inorganic materials 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- NFMAZVUSKIJEIH-UHFFFAOYSA-N bis(sulfanylidene)iron Chemical compound S=[Fe]=S NFMAZVUSKIJEIH-UHFFFAOYSA-N 0.000 description 2
- 238000001354 calcination Methods 0.000 description 2
- BUGICWZUDIWQRQ-UHFFFAOYSA-N copper iron sulfane Chemical compound S.[Fe].[Cu] BUGICWZUDIWQRQ-UHFFFAOYSA-N 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- XLYOFNOQVPJJNP-ZSJDYOACSA-N heavy water Substances [2H]O[2H] XLYOFNOQVPJJNP-ZSJDYOACSA-N 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 229910052500 inorganic mineral Inorganic materials 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000011707 mineral Substances 0.000 description 2
- 230000009467 reduction Effects 0.000 description 2
- 229910002703 Al K Inorganic materials 0.000 description 1
- 229910017518 Cu Zn Inorganic materials 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 238000012993 chemical processing Methods 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 229910052681 coesite Inorganic materials 0.000 description 1
- 229910052906 cristobalite Inorganic materials 0.000 description 1
- 238000005188 flotation Methods 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 239000010437 gem Substances 0.000 description 1
- 229910001751 gemstone Inorganic materials 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- JKQOBWVOAYFWKG-UHFFFAOYSA-N molybdenum trioxide Chemical compound O=[Mo](=O)=O JKQOBWVOAYFWKG-UHFFFAOYSA-N 0.000 description 1
- 229910052755 nonmetal Inorganic materials 0.000 description 1
- PQQKPALAQIIWST-UHFFFAOYSA-N oxomolybdenum Chemical compound [Mo]=O PQQKPALAQIIWST-UHFFFAOYSA-N 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 239000004065 semiconductor Substances 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 229910052682 stishovite Inorganic materials 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 229910052905 tridymite Inorganic materials 0.000 description 1
- 239000002351 wastewater Substances 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
- C25C—PROCESSES FOR THE ELECTROLYTIC PRODUCTION, RECOVERY OR REFINING OF METALS; APPARATUS THEREFOR
- C25C1/00—Electrolytic production, recovery or refining of metals by electrolysis of solutions
- C25C1/22—Electrolytic production, recovery or refining of metals by electrolysis of solutions of metals not provided for in groups C25C1/02 - C25C1/20
-
- C—CHEMISTRY; METALLURGY
- C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
- C25C—PROCESSES FOR THE ELECTROLYTIC PRODUCTION, RECOVERY OR REFINING OF METALS; APPARATUS THEREFOR
- C25C1/00—Electrolytic production, recovery or refining of metals by electrolysis of solutions
- C25C1/06—Electrolytic production, recovery or refining of metals by electrolysis of solutions or iron group metals, refractory metals or manganese
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22B—PRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
- C22B3/00—Extraction of metal compounds from ores or concentrates by wet processes
- C22B3/04—Extraction of metal compounds from ores or concentrates by wet processes by leaching
- C22B3/045—Leaching using electrochemical processes
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22B—PRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
- C22B34/00—Obtaining refractory metals
- C22B34/30—Obtaining chromium, molybdenum or tungsten
- C22B34/34—Obtaining molybdenum
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P10/00—Technologies related to metal processing
- Y02P10/20—Recycling
Definitions
- the present invention relates to a method of leaching molybdenum (Mo) from a sulfide mineral containing molybdenum (Mo) and copper (Cu) through an electrolytic oxidation scheme.
- Mo molybdenum
- the Mo has a significant extensive application field including a tank, a vehicle, machine, paint, a reagent, a semiconductor, and an electric furnace from a military industry to electric and electronic part fields.
- the demand for Mo is rapidly increased in China since 2003 and the demand for iron ore are increased all around the world, the price of the Mo has been sharply raised.
- MoS 2 molybdenite
- CuFeS 2 chalcopyrite
- FeS 2 pyrite
- MoO 3 molybdenum oxide
- Mo may be leached using sulfuric acid. According to the leaching scheme using the sulfuric acid, only copper (Cu) is not selectively leached, but a great amount of Mo is eluted together. Due to the lack of domestic technologies, all leached wastewater containing a great amount of Mo has been wasted
- the present invention provides a method of selectively leaching only molybdenum from sulfide mineral through an electrolytic oxidation scheme.
- a method of leaching molybdenum (Mo) from the sulfide mineral containing molybdenum (Mo) and copper (Cu) through the electrolytic oxidation scheme includes dipping the sulfide mineral containing the molybdenum (Mo) and the copper (Cu) into a solution having chloride dissolved therein, loading an electrode into the solution, and then applying a current to the solution.
- the sulfide mineral containing the molybdenum (Mo) and the copper (Cu) is a molybdenum disulfide (MoS 2 ).
- the chloride comprises at least one selected from the group consisting of NaCl, KCl, and NH 4 Cl.
- the chloride has a concentration in a range of 1 M to 6 M.
- An anode of the electrode comprises one selected from the group consisting of platinum (Pt), iridium dioxide (IrO 2 ), stainless steel, gold (Au), silver (Ag), titanium (Ti), zirconium (Zr), iron (Fe), cobalt (Co), and nickel (Ni).
- a cathode of the electrode comprises one selected from the group consisting of glassy carbon, platinum (Pt), gold (Au), iridium dioxide (IrO 2 ), and graphite.
- the current is in a range of 10 mA/cm 2 to 100 mA/cm 2 .
- the solution has a temperature in a range of 25° C. to 80° C. when the current is applied.
- the solution has pH of 9 when the current is applied.
- a method of leaching molybdenum (Mo) from the sulfide mineral containing molybdenum (Mo) and copper (Cu) through the electrolytic oxidation scheme which includes dipping the sulfide mineral containing the molybdenum (Mo) and the copper (Cu) into a solution having chloride dissolved therein, loading an electrode into the solution, and then applying a current to the solution, in which an ultrasonic wave is irradiated when the current is applied.
- the ultrasonic wave is irradiated while supplying power in a range of 15 W to 65 W at a frequency of 20 kHz.
- the present invention is suggested by solving the problem of the related art in which a great amount of Cu is contained in Mo when Mo is leached from a sulfide mineral, so that the quality of the Mo is degraded. Therefore, according to the present invention, only Mo not only can be selectively leached from the sulfide mineral, but also high-quality Mo (less than 0.5% of Cu and 50% or more of Mo) can be retrieved.
- the sulfide mineral can be decomposed and leached by electrochemically producing an oxidation agent without separately adding an oxidation agent through an electrolytic oxidation scheme, which is eco-friendly.
- the process is simple and cost is reduced.
- a process of irradiating an ultraviolet wave is applied to the leaching process of the Mo, so that the leaching yield of the Mo can be improved to 90% or more.
- FIG. 1 is a flowchart showing a method of leaching Mo from a sulfide mineral containing Mo and Cu through an electrolytic oxidation scheme according to the present invention.
- FIG. 2 is a schematic view showing an electrolytic oxidation device in the method of leaching Mo from the sulfide mineral containing Mo and Cu through the electrolytic oxidation scheme according to the present invention.
- FIG. 3 is a graph showing a leaching yield of Mo as a function of reaction time in the method of leaching Mo from the sulfide mineral containing Mo and Cu through the electrolytic oxidation scheme according to the present invention.
- FIG. 4 is a graph showing a leaching yield of Mo as a function of the pH of a solution in the method of leaching Mo from the sulfide mineral containing Mo and Cu through the electrolytic oxidation scheme according to the present invention.
- FIG. 5 is a graph showing a leaching yield of Mo as a function of a reaction temperature in the method of leaching Mo from the sulfide mineral containing Mo and Cu through the electrolytic oxidation scheme according to the present invention.
- FIG. 6 is a graph showing a leaching yield of Mo, Cu, and Fe in the method of leaching Mo from the sulfide mineral containing Mo and Cu through the electrolytic oxidation scheme according to the present invention.
- FIG. 7 is a graph showing leaching yields according to the irradiation of an ultrasonic wave in the method of leaching Mo from the sulfide mineral containing Mo and Cu through the electrolytic oxidation scheme according to the present invention.
- the present invention provides a method of leaching molybdenum (Mo) from a sulfide mineral containing molybdenum (Mo) and copper (Cu) through an electrolytic oxidation scheme, characterized in that the sulfide mineral containing molybdenum (Mo) and copper (Cu) is dipped into a solution having chloride dissolved therein and an electrode is loaded into the solution to apply a current to the solution.
- the method of leaching Mo from the sulfide mineral containing Mo and Cu through the electrolytic oxidation scheme of the present invention is made in order to solve the problem of the related art in which a great amount of Cu is contained in Mo when Mo is leached from a sulfide mineral, so that the quality of the Mo is degraded. Therefore, according to the method of leaching Mo from the sulfide mineral containing Mo and Cu through the electrolytic oxidation scheme of the present invention, only Mo not only can be selectively leached from the sulfide mineral, but also high-quality Mo (less than 0.5% of Cu and 50% or more of Mo) can be retrieved.
- the sulfide mineral is decomposed and leached by electrochemically producing an oxidation agent without separately adding an oxidation agent through an electrolytic oxidation scheme, which is eco-friendly.
- the process is simple and cost is reduced.
- a process of irradiating an ultraviolet wave is applied to the leaching process of the Mo, so that the leaching yield of the Mo can be improved to 90% or more.
- FIG. 1 is a flowchart showing the method of leaching No from a sulfide mineral containing Mo and Cu through an electrolytic oxidation scheme according to the present invention.
- the present invention will be described in detail with reference to FIG. 1 .
- the method of leaching Mo from the sulfide mineral containing Mo and Cu through the electrolytic oxidation scheme according to the present invention includes step S 100 of dipping the sulfide mineral containing Mo and Cu into a solution having chloride dissolved therein.
- the sulfide mineral which is the mixture of metal or non-metal and sulfur, occupies 0.15% of a land.
- the sulfide mineral is economically advantageous.
- the sulfide mineral containing Mo and Cu according to the present invention is ore mined from the Geum-um mine located at Hupoup, Uljin-gun, Gyeonsangbuk-do, Republic of Korea.
- the present invention provides a method of leaching only Mo without an additional process to remove Cu from the low-quality concentrate and retrieve high-quality Mo.
- the chloride may include at least one selected from the group consisting of NaCl, KCl, and NH 4 Cl, and preferably has the concentration of 1 M to 6M. If the concentration of the chloride is less than 1 M, the leaching yield may be degraded. If the concentration of the chloride exceeds 6M, the leaching yield is not increased any more. Accordingly, the concentration of the chloride is preferably 6 M or less in terms of energy saving.
- the method of leaching Mo from the sulfide mineral containing Mo and Cu through the electrolytic oxidation scheme according to the present invention includes step S 200 of loading an electrode into the solution and applying the current.
- FIG. 2 is a schematic view showing an electrolytic oxidation device in the method of leaching Mo from the sulfide mineral containing Mo and Cu through the electrolytic oxidation scheme according to the present invention.
- the electrode is loaded and the current is applied.
- Cl 2 gas is generated, and the generated Cl 2 reacts with the solution to produce ClO ⁇ .
- the ClO ⁇ is an ion having high oxidizing power to oxidize molybdenum disulfide (MoS 2 ), so that the molybdenum disulfide (MoS 2 ) is decomposed.
- the anode of the electrode may include platinum (Pt), iridium dioxide (IrO 2 ), stainless steel, gold (Au), silver (Ag), titanium (Ti), zirconium (Zr), iron (Fe), cobalt (Co), or nickel (Ni).
- the cathode of the electrode may include glassy carbon, platinum (Pt), gold (Au), iridium dioxide (IrO 2 ), and graphite. The electrolytic oxidation reaction and the chemical reaction occurring in the anode and the cathode are expressed in reaction formula 1 and reaction formula 2.
- the current is in the range of 10 mA/cm 2 to 100 mA/cm 2 . If the current is less than 10 mA/cm 2 , Cl 2 is not sufficiently produced, so that the leaching yield of molybdenum (Mo) is degraded. If the current exceeds 100 mA/cm 2 , the leaching yield of molybdenum (Mo) is not increased any more. Accordingly, it is preferred that the current is 100 mA/cm 2 or less in terms of energy saving.
- the pH of the solution is preferably 9. If the pH of the solution is 9, the leaching yield represents the highest value. If the pH of the solution is less than 9 or more than 9, the leaching yield of molybdenum (Mo) represents a low value.
- the solution temperature is preferably in the range of 25° C. to 80° C. If the solution temperature is less than 25° C., the leaching yield of molybdenum (Mo) represents a low value. If the solution temperature is more than 80° C., the solubility of Cl 2 is reduced, so that ClO ⁇ is less produced. Accordingly, the leaching yield of molybdenum (Mo) is degraded.
- the present invention provides the method of leaching Mo from the sulfide mineral containing Mo and Cu through the electrolytic oxidation scheme, characterized in that the method includes a step of dipping the sulfide mineral containing molybdenum (Mo) and copper (Cu) into the solution having chloride dissolved therein, loading the electrode into the solution and applying a current to the solution, and an ultrasonic wave is irradiated when the current is applied.
- Mo molybdenum
- Cu copper
- the ultrasonic wave is irradiated when the current is applied, the production of ClO ⁇ may be increased in the solution. Accordingly, the leaching yield of molybdenum (Mo) can be increased to 90% or more.
- the ultrasonic wave is preferably irradiated during the leaching reaction while supplying power of 15 W to 65 W at the frequency of 20 kHz. If the power is less than 15 W, an influence is significantly slightly exerted on the improvement of the leaching yield. If the power exceeds 65 W, the leaching yield is not improved any more. Accordingly, it is preferred that the power is 65 W in terms of power saving.
- Molybdenum (Mo) in the second embodiment was leached in the same manner as that of the first embodiment except that molybdenum disulfide (MoS 2 ), which was obtained by secondarily concentrating a mineral mined from the Geum-um mine located at Hupoup, Uljin-gun, Gyeonsangbuk-do, was used and 5M of NaCl was used.
- Molybdenum disulfide (MoS 2 ) which was obtained by secondarily concentrating a mineral mined from the Geum-um mine located at Hupoup, Uljin-gun, Gyeonsangbuk-do, was used and 5M of NaCl was used.
- Table 1 represents contents of the molybdenum disulfide (MoS 2 ) obtained through the secondary concentrate.
- Molybdenum (Mo) in the third embodiment was leached in the same manner as that of the second embodiment except that, when the current was applied, the ultrasonic wave was irradiated during the leaching reaction while supplying power of 65 W at the frequency of 20 kHz.
- the leaching yield is rapidly increased to 80% or more till 120 minutes, and then the increment of the leaching speed is decreased after 120 minutes. After 240 minutes, the high leaching yield corresponding to about 94% is shown.
- 91.3% of a Mo leaching yield is represented at pH 9, and the Mo leaching yield is decreased to 55.2% at pH 0, and more decreased to 8.4% at pH 14.
- the leaching yield is decreased at pH 0 because Mo is dissolved to MoO 4 2 ⁇ ions in the initial stage, and precipitated to MoO 3 according to the elapse of the time, so that an amount of Mo existing in the form of ions is decreased, and a portion of MoO 3 is precipitated on the surface of MoS 2 to restrain the reaction.
- NaOH is added to the solution, so that the pH of the solution is adjusted to the alkaline atmosphere of pH 9.
- the leaching yield of molybdenum (Mo) is increased and MoO 3 which is produced at pH 0, is re-dissolved at pH 0+Al (Alkali).
- the leaching yield represents a significantly low value at pH 14 because the oxidizing power of ClO ⁇ is reduced by the high pH.
- the oxidation/reduction potential of ClO ⁇ greatly depends on pH.
- the oxidation/reduction potential is rapidly reduced. Accordingly, the oxidizing power is reduced.
- the leaching yield of Mo is increased to 68% from 32%.
- the leaching yield is slightly decreased to 63% at 80° C.
- the reaction to produce Cl 2 is decreased at the carbon electrode as the temperature is increased. As Cl 2 solubility is decreased, the production of ClO ⁇ is decreased, so that the leaching yield may be reduced.
- the leaching yield of metal in the second embodiment was analyzed, and the result was shown in FIG. 6 .
- the leaching yield was analyzed according to the power variation of the ultrasonic wave in the third embodiment of irradiating the ultrasonic wave to the second embodiment, and the result was shown in FIG. 7 .
- the leaching yield of Mo is represented as 91.7%.
- the leaching yield is increased in the case of the ultrasonic wave is irradiated as compared with the case that the ultrasonic wave is not irradiated
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Abstract
Disclosed is a method of leaching molybdenum (Mo) from the sulfide mineral containing molybdenum (Mo) and copper (Cu) through the electrolytic oxidation scheme. The method includes dipping the sulfide mineral containing the molybdenum (Mo) and the copper (Cu) into a solution having chloride dissolved therein, loading an electrode into the solution, and then applying a current to the solution.
Description
- This application claims priority to Korean Patent Application No. 10-2013-0133501 filed on Nov. 5, 2013, and all the benefits accruing therefrom under 35 U.S.C. §119, the contents of which is incorporated by reference in its entirety.
- 1) Field of the Invention
- The present invention relates to a method of leaching molybdenum (Mo) from a sulfide mineral containing molybdenum (Mo) and copper (Cu) through an electrolytic oxidation scheme.
- 2) Background of Related Art
- Since molybdenum (Mo) has a superior thermal conductivity and a low thermal expansion coefficient, the Mo has a significant extensive application field including a tank, a vehicle, machine, paint, a reagent, a semiconductor, and an electric furnace from a military industry to electric and electronic part fields. As the demand for Mo is rapidly increased in China since 2003 and the demand for iron ore are increased all around the world, the price of the Mo has been sharply raised.
- Currently, in our country, low-quality molybdenum (Mo) has been produced and mined from the Geum-um mine located at Hupoup, Uljin-gun, Gyeonsangbuk-do, the Shinyemi mine located at Sin-dong, Jeongseon, Ganwon-do, and the Donwon mine located at Jecheon, Chungcheongbuk-do. In the case of the Geum-um mine, ore concentrate facilities have been constructed, and currently are in operation to produce 670 ton of concentrates by processing 900 ton of gemstones a day. In most domestic molybdenite (MoS2) mines, chalcopyrite (CuFeS2), which is sulfide mineral, and pyrite (FeS2) are produced together to degrade the quality of the concentrate as the above minerals are contained in the concentrate. Accordingly, currently, low-quality concentrates have been produced. Therefore, after the content of Mo is increased through a physical flotation step to refine Mo, a calcinations step is performed to make molybdenum oxide (MoO3) for use. In addition, Mo has been produced through a chemical leaching scheme and a chemical processing scheme having various process steps.
- Further, in order to lower the content of copper (Cu) to 0.5% or less, after performing a calcinations process for molybdenite (MoS2), Mo may be leached using sulfuric acid. According to the leaching scheme using the sulfuric acid, only copper (Cu) is not selectively leached, but a great amount of Mo is eluted together. Due to the lack of domestic technologies, all leached wastewater containing a great amount of Mo has been wasted
- There is a related art which is Korea Unexamined Patent Publication No. 10-2011-0046024 (published on May 4, 2011) titled “method of leaching impurities contained in molybdenum oxide concentrate”.
- The present invention provides a method of selectively leaching only molybdenum from sulfide mineral through an electrolytic oxidation scheme.
- The objects of the present invention are not limited to the above-mentioned objects, and other objects will be clearly understood by those skilled in the art.
- In order to accomplish the above object, there is provided a method of leaching molybdenum (Mo) from the sulfide mineral containing molybdenum (Mo) and copper (Cu) through the electrolytic oxidation scheme. The method includes dipping the sulfide mineral containing the molybdenum (Mo) and the copper (Cu) into a solution having chloride dissolved therein, loading an electrode into the solution, and then applying a current to the solution.
- In this case, the sulfide mineral containing the molybdenum (Mo) and the copper (Cu) is a molybdenum disulfide (MoS2).
- The chloride comprises at least one selected from the group consisting of NaCl, KCl, and NH4Cl.
- The chloride has a concentration in a range of 1 M to 6 M.
- An anode of the electrode comprises one selected from the group consisting of platinum (Pt), iridium dioxide (IrO2), stainless steel, gold (Au), silver (Ag), titanium (Ti), zirconium (Zr), iron (Fe), cobalt (Co), and nickel (Ni). A cathode of the electrode comprises one selected from the group consisting of glassy carbon, platinum (Pt), gold (Au), iridium dioxide (IrO2), and graphite.
- The current is in a range of 10 mA/cm2 to 100 mA/cm2. The solution has a temperature in a range of 25° C. to 80° C. when the current is applied. In addition, the solution has pH of 9 when the current is applied.
- In addition, according to the embodiment, there is provided a method of leaching molybdenum (Mo) from the sulfide mineral containing molybdenum (Mo) and copper (Cu) through the electrolytic oxidation scheme, which includes dipping the sulfide mineral containing the molybdenum (Mo) and the copper (Cu) into a solution having chloride dissolved therein, loading an electrode into the solution, and then applying a current to the solution, in which an ultrasonic wave is irradiated when the current is applied.
- In this case, the ultrasonic wave is irradiated while supplying power in a range of 15 W to 65 W at a frequency of 20 kHz.
- As described above, the present invention is suggested by solving the problem of the related art in which a great amount of Cu is contained in Mo when Mo is leached from a sulfide mineral, so that the quality of the Mo is degraded. Therefore, according to the present invention, only Mo not only can be selectively leached from the sulfide mineral, but also high-quality Mo (less than 0.5% of Cu and 50% or more of Mo) can be retrieved.
- In addition, the sulfide mineral can be decomposed and leached by electrochemically producing an oxidation agent without separately adding an oxidation agent through an electrolytic oxidation scheme, which is eco-friendly. The process is simple and cost is reduced. A process of irradiating an ultraviolet wave is applied to the leaching process of the Mo, so that the leaching yield of the Mo can be improved to 90% or more.
-
FIG. 1 is a flowchart showing a method of leaching Mo from a sulfide mineral containing Mo and Cu through an electrolytic oxidation scheme according to the present invention. -
FIG. 2 is a schematic view showing an electrolytic oxidation device in the method of leaching Mo from the sulfide mineral containing Mo and Cu through the electrolytic oxidation scheme according to the present invention. -
FIG. 3 is a graph showing a leaching yield of Mo as a function of reaction time in the method of leaching Mo from the sulfide mineral containing Mo and Cu through the electrolytic oxidation scheme according to the present invention. -
FIG. 4 is a graph showing a leaching yield of Mo as a function of the pH of a solution in the method of leaching Mo from the sulfide mineral containing Mo and Cu through the electrolytic oxidation scheme according to the present invention. -
FIG. 5 is a graph showing a leaching yield of Mo as a function of a reaction temperature in the method of leaching Mo from the sulfide mineral containing Mo and Cu through the electrolytic oxidation scheme according to the present invention. -
FIG. 6 is a graph showing a leaching yield of Mo, Cu, and Fe in the method of leaching Mo from the sulfide mineral containing Mo and Cu through the electrolytic oxidation scheme according to the present invention. -
FIG. 7 is a graph showing leaching yields according to the irradiation of an ultrasonic wave in the method of leaching Mo from the sulfide mineral containing Mo and Cu through the electrolytic oxidation scheme according to the present invention. - Hereinafter, an example embodiment of the present invention will be described in detail with reference to accompanying drawings.
- The advantages, the features, and schemes of achieving the advantages and features of the present invention will be apparently comprehended by those skilled in the art based on the embodiments, which are detailed later in detail, together with accompanying drawings.
- The present invention is not limited to the following embodiments but includes various applications and modifications. The embodiments will make the disclosure of the present invention complete, and allow those skilled in the art to completely comprehend the scope of the present invention. The present invention is only defined within the scope of accompanying claims.
- In addition, the details of the generally-known technology that makes the subject matter of the present invention unclear will be omitted in the following description.
- The present invention provides a method of leaching molybdenum (Mo) from a sulfide mineral containing molybdenum (Mo) and copper (Cu) through an electrolytic oxidation scheme, characterized in that the sulfide mineral containing molybdenum (Mo) and copper (Cu) is dipped into a solution having chloride dissolved therein and an electrode is loaded into the solution to apply a current to the solution.
- The method of leaching Mo from the sulfide mineral containing Mo and Cu through the electrolytic oxidation scheme of the present invention is made in order to solve the problem of the related art in which a great amount of Cu is contained in Mo when Mo is leached from a sulfide mineral, so that the quality of the Mo is degraded. Therefore, according to the method of leaching Mo from the sulfide mineral containing Mo and Cu through the electrolytic oxidation scheme of the present invention, only Mo not only can be selectively leached from the sulfide mineral, but also high-quality Mo (less than 0.5% of Cu and 50% or more of Mo) can be retrieved. In addition, the sulfide mineral is decomposed and leached by electrochemically producing an oxidation agent without separately adding an oxidation agent through an electrolytic oxidation scheme, which is eco-friendly. The process is simple and cost is reduced. A process of irradiating an ultraviolet wave is applied to the leaching process of the Mo, so that the leaching yield of the Mo can be improved to 90% or more.
-
FIG. 1 is a flowchart showing the method of leaching No from a sulfide mineral containing Mo and Cu through an electrolytic oxidation scheme according to the present invention. Hereinafter, the present invention will be described in detail with reference toFIG. 1 . - The method of leaching Mo from the sulfide mineral containing Mo and Cu through the electrolytic oxidation scheme according to the present invention includes step S100 of dipping the sulfide mineral containing Mo and Cu into a solution having chloride dissolved therein.
- According to the method of leaching Mo from the sulfide mineral containing Mo and Cu through the electrolytic oxidation scheme according to the present invention, the sulfide mineral, which is the mixture of metal or non-metal and sulfur, occupies 0.15% of a land. However, since important metal is extracted from the sulfide mineral, the sulfide mineral is economically advantageous. The sulfide mineral containing Mo and Cu according to the present invention is ore mined from the Geum-um mine located at Hupoup, Uljin-gun, Gyeonsangbuk-do, Republic of Korea. In most domestic molybdenite (MoS2) mines, chalcopyrite (CuFeS2), which is sulfide mineral, and pyrite (FeS2) are produced together to degrade the quality of the concentrate as the above ores are contained in the concentrate. Therefore, the present invention provides a method of leaching only Mo without an additional process to remove Cu from the low-quality concentrate and retrieve high-quality Mo.
- In the method of leaching Mo from the sulfide mineral containing Mo and Cu through the electrolytic oxidation scheme according to the present invention, the chloride may include at least one selected from the group consisting of NaCl, KCl, and NH4Cl, and preferably has the concentration of 1 M to 6M. If the concentration of the chloride is less than 1 M, the leaching yield may be degraded. If the concentration of the chloride exceeds 6M, the leaching yield is not increased any more. Accordingly, the concentration of the chloride is preferably 6 M or less in terms of energy saving.
- The method of leaching Mo from the sulfide mineral containing Mo and Cu through the electrolytic oxidation scheme according to the present invention includes step S200 of loading an electrode into the solution and applying the current.
-
FIG. 2 is a schematic view showing an electrolytic oxidation device in the method of leaching Mo from the sulfide mineral containing Mo and Cu through the electrolytic oxidation scheme according to the present invention. Referring toFIG. 2 , after the sulfide mineral containing Mo and Cu has been dipped into the solution having the chloride dissolved therein, the electrode is loaded and the current is applied. In this case, Cl2 gas is generated, and the generated Cl2 reacts with the solution to produce ClO−. The ClO− is an ion having high oxidizing power to oxidize molybdenum disulfide (MoS2), so that the molybdenum disulfide (MoS2) is decomposed. Accordingly, Mo ions are leached. In this case, the anode of the electrode may include platinum (Pt), iridium dioxide (IrO2), stainless steel, gold (Au), silver (Ag), titanium (Ti), zirconium (Zr), iron (Fe), cobalt (Co), or nickel (Ni). The cathode of the electrode may include glassy carbon, platinum (Pt), gold (Au), iridium dioxide (IrO2), and graphite. The electrolytic oxidation reaction and the chemical reaction occurring in the anode and the cathode are expressed in reaction formula 1 and reaction formula 2. -
Anode: 2Cl−→Cl2+2e −, E0=1.228VSHE(standard hydrogen electrode) -
Cathode: 2H2O+2e −→2OH−+H2, E0=0VSHE(standard hydrogen electrode) [Reaction formula 1] -
Cl2+2O−→ClO−+Cl−+H2O -
MoS2+6ClO+−+4OH−→MoO4 2−+SO4 2−+S+6Cl−+2H2O -
S+3ClO−+H2O→H2SO4+3C− [Reaction formula 2] - In the method of leaching Mo from the sulfide mineral containing Mo and Cu through the electrolytic oxidation scheme according to the present invention, it is preferred that the current is in the range of 10 mA/cm2 to 100 mA/cm2. If the current is less than 10 mA/cm2, Cl2 is not sufficiently produced, so that the leaching yield of molybdenum (Mo) is degraded. If the current exceeds 100 mA/cm2, the leaching yield of molybdenum (Mo) is not increased any more. Accordingly, it is preferred that the current is 100 mA/cm2 or less in terms of energy saving.
- When the current is applied to the solution, the pH of the solution is preferably 9. If the pH of the solution is 9, the leaching yield represents the highest value. If the pH of the solution is less than 9 or more than 9, the leaching yield of molybdenum (Mo) represents a low value.
- When the current is applied to the solution, the solution temperature is preferably in the range of 25° C. to 80° C. If the solution temperature is less than 25° C., the leaching yield of molybdenum (Mo) represents a low value. If the solution temperature is more than 80° C., the solubility of Cl2 is reduced, so that ClO− is less produced. Accordingly, the leaching yield of molybdenum (Mo) is degraded.
- In addition, the present invention provides the method of leaching Mo from the sulfide mineral containing Mo and Cu through the electrolytic oxidation scheme, characterized in that the method includes a step of dipping the sulfide mineral containing molybdenum (Mo) and copper (Cu) into the solution having chloride dissolved therein, loading the electrode into the solution and applying a current to the solution, and an ultrasonic wave is irradiated when the current is applied.
- In the method of leaching molybdenum (Mo) from the sulfide mineral containing molybdenum (Mo) and copper (Cu) through the electrolytic oxidation scheme according to the present invention, the ultrasonic wave is irradiated when the current is applied, the production of ClO− may be increased in the solution. Accordingly, the leaching yield of molybdenum (Mo) can be increased to 90% or more.
- The ultrasonic wave is preferably irradiated during the leaching reaction while supplying power of 15 W to 65 W at the frequency of 20 kHz. If the power is less than 15 W, an influence is significantly slightly exerted on the improvement of the leaching yield. If the power exceeds 65 W, the leaching yield is not improved any more. Accordingly, it is preferred that the power is 65 W in terms of power saving.
- After dipping MoS2 into a solution having 3 M of NaCl dissolved therein, a platinum (Pt) electrode and a glassy carbon electrode were loaded, and a current of 90 mA/cm2 was applied. In this case, the pulp density of MoS2 was 1% (w/v), the pH of the solution was adjusted to 9, and the solution temperature of the solution was increased to 50° C.
- Molybdenum (Mo) in the second embodiment was leached in the same manner as that of the first embodiment except that molybdenum disulfide (MoS2), which was obtained by secondarily concentrating a mineral mined from the Geum-um mine located at Hupoup, Uljin-gun, Gyeonsangbuk-do, was used and 5M of NaCl was used. Following table 1 represents contents of the molybdenum disulfide (MoS2) obtained through the secondary concentrate.
-
TABLE 1 SiO2 Fe Mg Al K Na MoS2 Cu Zn Secondary 1.93 13 0.1 1.15 0.14 0.03 68.24 8.61 0.53 Concentrate - Molybdenum (Mo) in the third embodiment was leached in the same manner as that of the second embodiment except that, when the current was applied, the ultrasonic wave was irradiated during the leaching reaction while supplying power of 65 W at the frequency of 20 kHz.
- In the method of leaching molybdenum (Mo) from the sulfide mineral containing molybdenum (Mo) and copper (Cu) through the electrolytic oxidation scheme according to the present invention, the leaching yield of the molybdenum (Mo) according to the leaching reaction time was analyzed, and the result was shown in
FIG. 3 . The molybdenum (Mo) was leached from MoS2 in the first embodiment. - As shown in
FIG. 3 , the leaching yield is rapidly increased to 80% or more till 120 minutes, and then the increment of the leaching speed is decreased after 120 minutes. After 240 minutes, the high leaching yield corresponding to about 94% is shown. - In the method of leaching molybdenum (Mo) from the sulfide mineral containing molybdenum (Mo) and copper (Cu) through the electrolytic oxidation scheme according to the present invention, the leaching yield of the molybdenum (Mo) according to the pH of the solution was analyzed, and the result was shown in
FIG. 4 . The molybdenum (Mo) was leached from MoS2 in the first embodiment. - Referring to
FIG. 4 , after the leaching has been performed for three hours while changing the pH of the solution, 91.3% of a Mo leaching yield is represented at pH 9, and the Mo leaching yield is decreased to 55.2% atpH 0, and more decreased to 8.4% at pH 14. The leaching yield is decreased atpH 0 because Mo is dissolved to MoO4 2−ions in the initial stage, and precipitated to MoO3 according to the elapse of the time, so that an amount of Mo existing in the form of ions is decreased, and a portion of MoO3 is precipitated on the surface of MoS2 to restrain the reaction. For example, after Mo is leached atpH 0, NaOH is added to the solution, so that the pH of the solution is adjusted to the alkaline atmosphere of pH 9. In this case, the leaching yield of molybdenum (Mo) is increased and MoO3 which is produced atpH 0, is re-dissolved atpH 0+Al (Alkali). Meanwhile, the leaching yield represents a significantly low value at pH 14 because the oxidizing power of ClO− is reduced by the high pH. In other words, the oxidation/reduction potential of ClO− greatly depends on pH. In addition, as the pH is increased, the oxidation/reduction potential is rapidly reduced. Accordingly, the oxidizing power is reduced. - In the method of leaching molybdenum (Mo) from the sulfide mineral containing molybdenum (Mo) and copper (Cu) through the electrolytic oxidation scheme according to the present invention, the leaching yield of the molybdenum (Mo) by changing the reaction temperature of Embodiment 2, and the result was shown in
FIG. 5 . - As shown in
FIG. 5 , if the reaction temperature is increased from 25° C. to 50° C., the leaching yield of Mo is increased to 68% from 32%. The leaching yield is slightly decreased to 63% at 80° C. The reaction to produce Cl2 is decreased at the carbon electrode as the temperature is increased. As Cl2 solubility is decreased, the production of ClO− is decreased, so that the leaching yield may be reduced. - The leaching yield of metal in the second embodiment was analyzed, and the result was shown in
FIG. 6 . In addition, the leaching yield was analyzed according to the power variation of the ultrasonic wave in the third embodiment of irradiating the ultrasonic wave to the second embodiment, and the result was shown inFIG. 7 . - As shown in
FIG. 6 , in the method of leaching molybdenum (Mo) from the sulfide mineral containing molybdenum (Mo) and copper (Cu) through the electrolytic oxidation scheme according to the present invention, Cu and Fe were not leached, but only Mo was selectively leached. - In addition, as shown in
FIG. 7 , when the ultrasonic wave is irradiated with the power of 65 W, the leaching yield of Mo is represented as 91.7%. In addition, the leaching yield is increased in the case of the ultrasonic wave is irradiated as compared with the case that the ultrasonic wave is not irradiated - Although the detailed embodiment of the method of leaching molybdenum (Mo) from the sulfide mineral containing molybdenum (Mo) and copper (Cu) through the electrolytic oxidation scheme according to the present invention has been described, it is obvious that various variations and modifications are possible.
- Although exemplary embodiments of the present invention have been described for the illustrative purpose, it is understood that the present invention should not be limited to these exemplary embodiments but various changes, modifications, equivalents can be made by one ordinary skilled in the art within the spirit and scope of the present invention as hereinafter claimed.
Claims (11)
1. A method of leaching molybdenum (Mo) from a sulfide mineral containing molybdenum (Mo) and copper (Cu) through an electrolytic oxidation scheme, the method comprising dipping the sulfide mineral containing the molybdenum (Mo) and the copper (Cu) into a solution having chloride dissolved therein, loading an electrode into the solution, and then applying a current to the solution,
wherein:
an ultrasonic wave is irradiated when the current is applied, the ultrasonic wave being irradiated while supplying power in a range of 15 W to 65 W at a frequency of 20 kHz, and
in the method of leaching molybdenum (Mo) from the sulfide mineral containing molybdenum (Mo) and copper (Cu), only Mo is leached and not Cu.
2. The method of claim 1 , wherein the sulfide mineral containing the molybdenum (Mo) and the copper (Cu) is a molybdenum disulfide (MoS2).
3. The method of claim 1 , wherein the chloride comprises at least one selected from the group consisting of NaCl, KCl, and NH4Cl.
4. The method of claim 1 , wherein the chloride has a concentration in a range of 1 M to 6 M.
5. The method of claim 1 , wherein an anode of the electrode comprises one selected from the group consisting of platinum (Pt), iridium dioxide (IrO2), stainless steel, gold (Au), silver (Ag), titanium (Ti), zirconium (Zr), iron (Fe), cobalt (Co), and nickel (Ni).
6. The method of claim 1 , wherein a cathode of the electrode comprises one selected from the group consisting of glassy carbon, platinum (Pt), gold (Au), iridium dioxide (IrO2), and graphite.
7. The method of claim 1 , wherein the current is in a range of 10 mA/cm2 to 100 mA/cm2.
8. The method of claim 1 , wherein the solution has a temperature in a range of 25° C. to 80° C. when the current is applied.
9. The method of claim 1 , wherein the solution has a pH of 9 when the current is applied.
10. (canceled)
11. (canceled)
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| KR10-2013-0133501 | 2013-11-05 | ||
| KR1020130133501A KR20150051691A (en) | 2013-11-05 | 2013-11-05 | Leaching method of molybdenum from sulfide mineral contained molybdenum and copper using electrolytic oxidation |
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| CN116159677A (en) * | 2021-11-24 | 2023-05-26 | 郑州大学 | Flotation separation method for copper-molybdenum bulk concentrate |
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| CN104032127B (en) * | 2014-06-10 | 2016-07-06 | 中南大学 | A kind of slurry electrolysis is the technique of Leaching Molybdenum from nickel-molybdenum ore |
| CN115446322A (en) * | 2022-09-22 | 2022-12-09 | 西北有色金属研究院 | A method of recycling waste molybdenum target to prepare molybdenum powder |
Citations (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3849265A (en) * | 1971-10-01 | 1974-11-19 | Us Interior | Electro-oxidative method for the recovery of molybdenum from sulfide ores |
| US4500496A (en) * | 1982-04-20 | 1985-02-19 | Brenda Mines Ltd. | Process for purifying molybdenite concentrates |
| US5487819A (en) * | 1992-06-26 | 1996-01-30 | Intec Pty Ltd | Production of metals from minerals |
| US20100011907A1 (en) * | 2006-09-13 | 2010-01-21 | Enpar Technologies Inc. | Extraction of metals from sulphide minerals |
| CN101717857A (en) * | 2009-08-18 | 2010-06-02 | 江苏大学 | Method for rapidly and directly dipping nickel sulfide concentrate under action of ultrasonic wave |
| US20120111150A1 (en) * | 2010-11-10 | 2012-05-10 | Meena Marafi | METHOD OR PROCESS FOR RECOVERING Mo, V, Ni, Co and Al FROM SPENT CATALYSTS USING ULTRASONIC ASSISTED LEACHING WITH EDTA |
| CN103352127A (en) * | 2013-04-07 | 2013-10-16 | 昆明理工大学 | Method for recovering zinc from zinc flue dust leaching residue through ultrasonic wave assistance |
-
2013
- 2013-11-05 KR KR1020130133501A patent/KR20150051691A/en not_active Ceased
- 2013-11-26 CN CN201310615641.3A patent/CN104611545A/en active Pending
- 2013-11-26 US US14/091,148 patent/US20150122667A1/en not_active Abandoned
Patent Citations (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3849265A (en) * | 1971-10-01 | 1974-11-19 | Us Interior | Electro-oxidative method for the recovery of molybdenum from sulfide ores |
| US4500496A (en) * | 1982-04-20 | 1985-02-19 | Brenda Mines Ltd. | Process for purifying molybdenite concentrates |
| US5487819A (en) * | 1992-06-26 | 1996-01-30 | Intec Pty Ltd | Production of metals from minerals |
| US20100011907A1 (en) * | 2006-09-13 | 2010-01-21 | Enpar Technologies Inc. | Extraction of metals from sulphide minerals |
| CN101717857A (en) * | 2009-08-18 | 2010-06-02 | 江苏大学 | Method for rapidly and directly dipping nickel sulfide concentrate under action of ultrasonic wave |
| US20120111150A1 (en) * | 2010-11-10 | 2012-05-10 | Meena Marafi | METHOD OR PROCESS FOR RECOVERING Mo, V, Ni, Co and Al FROM SPENT CATALYSTS USING ULTRASONIC ASSISTED LEACHING WITH EDTA |
| CN103352127A (en) * | 2013-04-07 | 2013-10-16 | 昆明理工大学 | Method for recovering zinc from zinc flue dust leaching residue through ultrasonic wave assistance |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN116159677A (en) * | 2021-11-24 | 2023-05-26 | 郑州大学 | Flotation separation method for copper-molybdenum bulk concentrate |
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