US20110290657A1 - Process for gold and silver leaching with thiourea solutions - Google Patents
Process for gold and silver leaching with thiourea solutions Download PDFInfo
- Publication number
- US20110290657A1 US20110290657A1 US12/926,715 US92671510A US2011290657A1 US 20110290657 A1 US20110290657 A1 US 20110290657A1 US 92671510 A US92671510 A US 92671510A US 2011290657 A1 US2011290657 A1 US 2011290657A1
- Authority
- US
- United States
- Prior art keywords
- thiourea
- gold
- solution
- silver
- leaching
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Abandoned
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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
- C25C1/20—Electrolytic production, recovery or refining of metals by electrolysis of solutions of noble metals
-
- 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
- C22B11/00—Obtaining noble metals
- C22B11/04—Obtaining noble metals by wet 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
- 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
- C22B3/16—Extraction of metal compounds from ores or concentrates by wet processes by leaching in organic solutions
- C22B3/1608—Leaching with acyclic or carbocyclic agents
- C22B3/1616—Leaching with acyclic or carbocyclic agents of a single type
- C22B3/1625—Leaching with acyclic or carbocyclic agents of a single type with amines
-
- 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 concerns the mining and mineral treatment industry. Specifically, it relates to a process that uses thiourea, electro-oxidized under controlled conditions, to form in-situ an oxidizing agent capable of dissolving gold and silver from minerals which contain them and the electrolytic recovery of said metals in the same process.
- cyanidation produces the highest yields in the majority of cases, however, with the problems of toxic residues and low efficiency in refractory minerals (those that contain organic material, arsenic or manganese) or those that contain high concentrations of silver sulfides.
- refractory minerals such as organic material, arsenic or manganese
- thiourea in acid media is a solution to the toxic waste problem since this method does not employ cyanide salts.
- Another impediment related to the use of thiourea is that the methods employed for precious metal recovery from the leaching solutions results in their contamination, limiting the possibility of their recycle within the process.
- One objective of the present invention is to avoid the harmful effects of the external oxidizing agents on the thiourea solutions.
- Another consists in recovering the gold and silver in their metallic form, once extracted from the mineral, in such a way that the electrical energy is employed in an optimal manner, by oxidizing part of the thiourea to formamidine disulfide in one of the compartments (anodic) and, in the other (cathodic), reducing the dissolved gold and silver reducing to their metallic state.
- our invention reduces the inconveniences of the instability of thiourea in the presence of strong oxidants, permitting at the same time a clean recovery of the metallic values, and constitutes an improvement of the solution employed for leaching gold and silver from minerals and other materials that contain them, employing thiourea.
- These improvements are characterized by the controlled electro-oxidation of 10 to 30% of the thiourea originally in the solution and the simultaneous electrowinning of the gold and silver from said solution.
- it consists of a process which allows the application of this solution in a process which extracts and recovers the metallic values from the minerals which contain them.
- the electrochemical cell is formed by the cathodic and the anodic compartments, separated by a membrane.
- the thiourea is partially oxidized, while in the cathodic compartment, the metals are reduced to their metallic form.
- FIG. 1 illustrates a block diagram of the process, subject of the present application.
- the first oxidation product of the thiourea is capable of selectively oxidizing gold and silver containing minerals, liberating the metals so that they may complex with the remaining thiourea and dissolve in the leaching solution.
- FADS formamidine disulfide
- an acid thiourea solution ( 1 ) is introduced into the electrolytic cell in the anodic compartment (ANODIC), where the thiourea is partially oxidized by an electrical current, applied under controlled conditions, to formamidine disulfide (FADS).
- ANODIC anodic compartment
- FADS amidine disulfide
- the partially oxidized solution ( 2 ) is sent to the leaching reactor, where it is mixed with mineral rich in metal values ( 3 ), during a period stipulated for the gold and silver dissolution.
- the mixture of pregnant solution (rich in precious metals) and the mineral residue (gangue) ( 4 ) is sent to a solid ( 5 )-liquid ( 6 ) separation step [L/S].
- the solid residue is discarded in the conventional manner (tailing dam).
- the pregnant solution enters into the cathodic compartment [CATHODIC] of the electrolytic cell, where the metals are reduced and electrodeposited.
- the solution now with a low metallic ion content, along with a part of the metallic gold and silver ( 7 ) is sent to another solid ( 8 )-liquid ( 9 ) separation stage [L/S] to recover the values.
- the resulting stream is made-up with reagents ( 11 ) in order to bring the concentrations of the solution up to the initial conditions of ( 1 ).
- the silver extraction was increased 36% with respect to the amount leached with an equivalent amount of cyanide.
- the pregnant solution was subjected to an electrolysis in the cathodic compartment of the same cell, where the thiourea was oxidized. After 2 hours, 98% of the silver and 92% of the gold present in the solution was precipitated.
Abstract
A solution composition that permits the use of thiourea is provided. The process is to form a solution that improves, on one hand, the velocity of gold and silver extraction, from minerals and other materials that contain them, improving the stability of the thiourea in the leaching solution and, on the other, the direct electrorecovery of the metals from the solution. The leaching solution, beforehand or simultaneously, has been subjected to a controlled electro-oxidation to produce formamidine disulfide (FADS) which acts as an oxidizing agent for the mineral phases that contain the gold and silver. In a preferred mode, the FADS is present as 10 to 30% of the total thiourea contained in the solution and the electrodeposition of the metals is performed in the same cell (cathodic compartment) in which the FADS is formed (anodic compartment).
Description
- This application is a continuation of co-pending application Ser. No. 10/567,108, filed on Aug. 6, 2007, and for which priority is claimed under 35 U.S.C. §120; which is the National Stage of International Application No. PCT/MX2004/000054 filed on Jul. 30, 2004, which in turn claims priority from Mexican Application PA/A/2003/006955, filed Aug. 4, 2003; the entire contents of all are hereby incorporated by reference
- The present invention concerns the mining and mineral treatment industry. Specifically, it relates to a process that uses thiourea, electro-oxidized under controlled conditions, to form in-situ an oxidizing agent capable of dissolving gold and silver from minerals which contain them and the electrolytic recovery of said metals in the same process.
- At present, the processing of gold and silver ores fundamentally depends on the form in which they are found in the mineral, using for this flotation, amalgamation and/or leaching. In this last technique, the solution employed plays an important role in the efficiency and environmental impact of the process.
- Basically two commercially implemented leaching techniques exist: cyanidation produces the highest yields in the majority of cases, however, with the problems of toxic residues and low efficiency in refractory minerals (those that contain organic material, arsenic or manganese) or those that contain high concentrations of silver sulfides. The use of thiourea in acid media is a solution to the toxic waste problem since this method does not employ cyanide salts.
- One of the great obstacles for the industrialization of the thiourea process to extract silver and gold is the instability of the thiourea solutions themselves. In the presence of strong oxidizing agents, such as ferric ion or hydrogen peroxide, the thiourea irreversibly oxidizes to form a species that is not active for complexing gold and silver.
- Another impediment related to the use of thiourea is that the methods employed for precious metal recovery from the leaching solutions results in their contamination, limiting the possibility of their recycle within the process.
- Additionally, there exists a disequilibrium with respect to the utilization of electrical energy; on one side of the electrolytic cell, the thiourea is being partially oxidized while, on the other side, separated by a membrane, the generated potential is being wasted on a sacrifice reduction process.
- One objective of the present invention is to avoid the harmful effects of the external oxidizing agents on the thiourea solutions.
- Another consists in recovering the gold and silver in their metallic form, once extracted from the mineral, in such a way that the electrical energy is employed in an optimal manner, by oxidizing part of the thiourea to formamidine disulfide in one of the compartments (anodic) and, in the other (cathodic), reducing the dissolved gold and silver reducing to their metallic state.
- Other objectives and advantages, that apply the principles and are derived from the present invention may be apparent from the study of the following description and diagrams that are included here for illustrative and not limitative purposes.
- In summary, our invention reduces the inconveniences of the instability of thiourea in the presence of strong oxidants, permitting at the same time a clean recovery of the metallic values, and constitutes an improvement of the solution employed for leaching gold and silver from minerals and other materials that contain them, employing thiourea. These improvements are characterized by the controlled electro-oxidation of 10 to 30% of the thiourea originally in the solution and the simultaneous electrowinning of the gold and silver from said solution. On the other hand, it consists of a process which allows the application of this solution in a process which extracts and recovers the metallic values from the minerals which contain them.
- For this purpose, the electrochemical cell is formed by the cathodic and the anodic compartments, separated by a membrane. In the anodic compartment, the thiourea is partially oxidized, while in the cathodic compartment, the metals are reduced to their metallic form.
- In order to better understand the characteristics of the invention, the following description is accompanied by a diagram, which forms an integral part of the same and is meant to be illustrative but not limitative:
-
FIG. 1 illustrates a block diagram of the process, subject of the present application. - To better understand the invention, a detailed description of the process shown in the diagram will be presented, which is annexed and meant to be illustrative but not limitative
- After having performed many experiments, it was found that the first oxidation product of the thiourea, formamidine disulfide (FADS), is capable of selectively oxidizing gold and silver containing minerals, liberating the metals so that they may complex with the remaining thiourea and dissolve in the leaching solution.
- Briefly, the process occurs in the following manner, observing
FIG. 1 : an acid thiourea solution (1) is introduced into the electrolytic cell in the anodic compartment (ANODIC), where the thiourea is partially oxidized by an electrical current, applied under controlled conditions, to formamidine disulfide (FADS). - The larger the quantity of thiourea partially oxidized, the better the performance of the solution. However, considering the price of thiourea, it is important to point out that the electro-oxidation should be executed at low voltages and in a proportion no greater than 30% with respect to the total quantity of thiourea in solution in order to achieve the reversible oxidation of the thiourea.
- The partially oxidized solution (2) is sent to the leaching reactor, where it is mixed with mineral rich in metal values (3), during a period stipulated for the gold and silver dissolution. Once the leaching is finished, the mixture of pregnant solution (rich in precious metals) and the mineral residue (gangue) (4) is sent to a solid (5)-liquid (6) separation step [L/S]. The solid residue is discarded in the conventional manner (tailing dam). On the other hand, the pregnant solution enters into the cathodic compartment [CATHODIC] of the electrolytic cell, where the metals are reduced and electrodeposited. The solution, now with a low metallic ion content, along with a part of the metallic gold and silver (7) is sent to another solid (8)-liquid (9) separation stage [L/S] to recover the values. After purging a small quantity of solution (10), the resulting stream is made-up with reagents (11) in order to bring the concentrations of the solution up to the initial conditions of (1).
- To better understand the invention, one of the many experiments is included as an example, where the adequate quantities of FADS generated in-situ and gold and silver recovery from the pregnant solution (after leaching) were determined.
- One liter of aqueous solution containing 15.2 grams of thiourea, with the pH adjusted to 2 with sulfuric acid, was subjected to a reversible potential of 500 mV for 2 hours in a membrane cell, where the anodic and cathodic compartments are separated, to produce in-situ a quantity of FADS, equivalent to the oxidation of 18% of the initial thiourea. Following this step, the solution is placed in contact with 10 grams of sulfide concentrate which contains approximately 8 wt. % silver and 0.08 wt. % gold for 60 hours. After this time, 95% of the original thiourea was intact and more than 94% of the silver and 65% of the gold contained in the mineral were leached. The silver extraction was increased 36% with respect to the amount leached with an equivalent amount of cyanide. After removal of the solid residue, the pregnant solution was subjected to an electrolysis in the cathodic compartment of the same cell, where the thiourea was oxidized. After 2 hours, 98% of the silver and 92% of the gold present in the solution was precipitated.
- The variations that the process might have for the electro-oxidation of the thiourea could be in the FADS concentration required in the leaching solution and the percentage of this component with respect to the quantity of mineral to be treated and the silver and gold concentrations that these may contain. However, if at any time an electro-oxidizes solution is employed, the process will be considered within the scope of the invention described in the present application
- The invention has been sufficiently described so that a person knowledgeable in the field could reproduce it and obtain the results that we mentioned in the present invention. Any person competent in the field of the present invention is capable of making modifications not described in the present application, however, if the application of these modifications on any material or in the manufacturing process of the same require any part of the process mentioned in the following claims, the material and process should be considered included within the scope of the invention.
Claims (5)
1. Improvement of the thiourea solutions to leach silver and gold characterized by containing a quantity of partially electro-oxidized thiourea.
2. Improvement of the thiourea solutions to leach silver and gold according to claim 1 , characterized additionally by a solution which contains formamidine disulfide (FADS) produced in-situ by a controlled electro-oxidation in a proportion of 10 to 30% of the total amount of thiourea contained in the solution.
3. Improvement of the thiourea solutions to leach silver and gold, according to claim 1 wherein the composition of the thiourea leaching solution is formulated in the same process in which the leaching solution is placed in contact with the mineral from which silver and gold values are to be leached.
4. Improvement of the thiourea solutions to leach silver and gold, according to claim 2 wherein the composition of the thiourea leaching solution is formulated in the same process in which the leaching solution is placed in contact with the mineral from which silver and gold values are to be leached.
5. Gold and silver leaching and recovery process with partially oxidized thiourea characterized as consisting of the thiourea oxidation by the application of an electrical current in a membrane cell, where the anodic and cathodic compartments are separated, before sending the product to the leaching stage and that after leaching is concluded, the pregnant solution, separated from the mineral residue (gangue), enters the cathodic compartment of the same electrolytic cell in which the thiourea was partially oxidized in the anodic part, where the metals are reduced and electrodeposited.
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US12/926,715 US20110290657A1 (en) | 2003-08-04 | 2010-12-06 | Process for gold and silver leaching with thiourea solutions |
US13/684,374 US20130140186A1 (en) | 2003-08-04 | 2012-11-23 | Process for gold and silver leaching with thiourea solutions |
Applications Claiming Priority (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
MXPA/A/2003/006955 | 2003-08-04 | ||
MXPA03006955A MXPA03006955A (en) | 2003-08-04 | 2003-08-04 | Silver and gold leaching and recovery process with electro-oxidised thiourea solutions. |
PCT/MX2004/000054 WO2005028687A1 (en) | 2003-08-04 | 2004-07-30 | Improvement to silver and gold leaching method with thiourea solutions |
US56710807A | 2007-08-06 | 2007-08-06 | |
US12/926,715 US20110290657A1 (en) | 2003-08-04 | 2010-12-06 | Process for gold and silver leaching with thiourea solutions |
Related Parent Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/MX2004/000054 Continuation WO2005028687A1 (en) | 2003-08-04 | 2004-07-30 | Improvement to silver and gold leaching method with thiourea solutions |
US56710807A Continuation | 2003-08-04 | 2007-08-06 |
Related Child Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US13/684,374 Continuation US20130140186A1 (en) | 2003-08-04 | 2012-11-23 | Process for gold and silver leaching with thiourea solutions |
Publications (1)
Publication Number | Publication Date |
---|---|
US20110290657A1 true US20110290657A1 (en) | 2011-12-01 |
Family
ID=34374329
Family Applications (3)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US10/567,108 Abandoned US20070272055A1 (en) | 2003-08-04 | 2004-07-30 | Process for Gold and Silver Leaching with Thiourea Solutions |
US12/926,715 Abandoned US20110290657A1 (en) | 2003-08-04 | 2010-12-06 | Process for gold and silver leaching with thiourea solutions |
US13/684,374 Abandoned US20130140186A1 (en) | 2003-08-04 | 2012-11-23 | Process for gold and silver leaching with thiourea solutions |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US10/567,108 Abandoned US20070272055A1 (en) | 2003-08-04 | 2004-07-30 | Process for Gold and Silver Leaching with Thiourea Solutions |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US13/684,374 Abandoned US20130140186A1 (en) | 2003-08-04 | 2012-11-23 | Process for gold and silver leaching with thiourea solutions |
Country Status (9)
Country | Link |
---|---|
US (3) | US20070272055A1 (en) |
EP (1) | EP1666613A1 (en) |
AU (1) | AU2004274823A1 (en) |
BR (1) | BRPI0412962A (en) |
CA (1) | CA2534737A1 (en) |
MX (1) | MXPA03006955A (en) |
NO (1) | NO20061067L (en) |
WO (1) | WO2005028687A1 (en) |
ZA (1) | ZA200601834B (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP3283661A4 (en) * | 2015-04-17 | 2018-10-17 | The University Of British Columbia | Process for leaching metal sulfides with reagents having thiocarbonyl functional groups |
US11859263B2 (en) | 2016-10-19 | 2024-01-02 | Jetti Resources, Llc | Process for leaching metal sulfides with reagents having thiocarbonyl functional groups |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US11312646B2 (en) * | 2014-08-08 | 2022-04-26 | Wisconsin Alumni Research Foundation | Method to remediate effluents containing metals complexed with organic and/or inorganic species |
GB201521633D0 (en) * | 2015-12-08 | 2016-01-20 | Saifa Technology Ltd | Cash drawer |
CA3160449A1 (en) * | 2021-05-17 | 2022-08-02 | Jetti Resources, Llc | Methods for liberating precious metals using a reagent having a thiocarbonyl functional group |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2349876B (en) * | 1999-05-10 | 2003-03-05 | Rio Tinto Technology Dev Ltd | Process for the Recovery of Noble Metals |
US6660059B2 (en) * | 2000-05-19 | 2003-12-09 | Placer Dome Technical Services Limited | Method for thiosulfate leaching of precious metal-containing materials |
-
2003
- 2003-08-04 MX MXPA03006955A patent/MXPA03006955A/en active IP Right Grant
-
2004
- 2004-07-30 WO PCT/MX2004/000054 patent/WO2005028687A1/en active Application Filing
- 2004-07-30 CA CA002534737A patent/CA2534737A1/en not_active Abandoned
- 2004-07-30 US US10/567,108 patent/US20070272055A1/en not_active Abandoned
- 2004-07-30 EP EP04748572A patent/EP1666613A1/en not_active Withdrawn
- 2004-07-30 BR BRPI0412962-8A patent/BRPI0412962A/en not_active Application Discontinuation
- 2004-07-30 AU AU2004274823A patent/AU2004274823A1/en not_active Abandoned
-
2006
- 2006-03-03 ZA ZA200601834A patent/ZA200601834B/en unknown
- 2006-03-06 NO NO20061067A patent/NO20061067L/en not_active Application Discontinuation
-
2010
- 2010-12-06 US US12/926,715 patent/US20110290657A1/en not_active Abandoned
-
2012
- 2012-11-23 US US13/684,374 patent/US20130140186A1/en not_active Abandoned
Cited By (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP3283661A4 (en) * | 2015-04-17 | 2018-10-17 | The University Of British Columbia | Process for leaching metal sulfides with reagents having thiocarbonyl functional groups |
US10781502B2 (en) | 2015-04-17 | 2020-09-22 | The University Of British Columbia | Process for leaching metal sulfides with reagents having thiocarbonyl functional groups |
US10865460B2 (en) | 2015-04-17 | 2020-12-15 | The University Of British Columbia | Process for leaching metal sulfides with reagents having thiocarbonyl functional groups |
US10870903B2 (en) | 2015-04-17 | 2020-12-22 | The University Of British Columbia | Process for leaching metal sulfides with reagents having thiocarbonyl functional groups |
US10876187B2 (en) | 2015-04-17 | 2020-12-29 | The University Of British Columbia | Process for leaching metal sulfides with reagents having thiocarbonyl functional groups |
US10876186B2 (en) | 2015-04-17 | 2020-12-29 | The University Of British Columbia | Process for leaching metal sulfides with reagents having thiocarbonyl functional groups |
US10954583B2 (en) | 2015-04-17 | 2021-03-23 | The University Of British Columbia | Process for leaching metal sulfides with reagents having thiocarbonyl functional groups |
US10961604B2 (en) | 2015-04-17 | 2021-03-30 | The University Of British Columbia | Process for leaching metal sulfides with reagents having thiocarbonyl functional groups |
US11884993B2 (en) | 2015-04-17 | 2024-01-30 | Jetti Resources, Llc | Process for leaching metal sulfides with reagents having thiocarbonyl functional groups |
US11859263B2 (en) | 2016-10-19 | 2024-01-02 | Jetti Resources, Llc | Process for leaching metal sulfides with reagents having thiocarbonyl functional groups |
Also Published As
Publication number | Publication date |
---|---|
BRPI0412962A (en) | 2006-09-26 |
WO2005028687A1 (en) | 2005-03-31 |
EP1666613A1 (en) | 2006-06-07 |
MXPA03006955A (en) | 2005-02-09 |
US20130140186A1 (en) | 2013-06-06 |
US20070272055A1 (en) | 2007-11-29 |
ZA200601834B (en) | 2007-09-26 |
NO20061067L (en) | 2006-04-26 |
AU2004274823A1 (en) | 2005-03-31 |
CA2534737A1 (en) | 2005-03-31 |
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