WO2020087189A1 - Nuevo proceso electroquimico basado en factor adimensional - Google Patents
Nuevo proceso electroquimico basado en factor adimensional Download PDFInfo
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- WO2020087189A1 WO2020087189A1 PCT/CL2019/050107 CL2019050107W WO2020087189A1 WO 2020087189 A1 WO2020087189 A1 WO 2020087189A1 CL 2019050107 W CL2019050107 W CL 2019050107W WO 2020087189 A1 WO2020087189 A1 WO 2020087189A1
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- WIPO (PCT)
- Prior art keywords
- process according
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- flow
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
- C25B—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES FOR THE PRODUCTION OF COMPOUNDS OR NON-METALS; APPARATUS THEREFOR
- C25B15/00—Operating or servicing cells
- C25B15/02—Process control or regulation
-
- 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
- C25C1/12—Electrolytic production, recovery or refining of metals by electrolysis of solutions of copper
-
- C—CHEMISTRY; METALLURGY
- C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
- C25C—PROCESSES FOR THE ELECTROLYTIC PRODUCTION, RECOVERY OR REFINING OF METALS; APPARATUS THEREFOR
- C25C7/00—Constructional parts, or assemblies thereof, of cells; Servicing or operating of cells
- C25C7/06—Operating or servicing
-
- 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 application is directed to a new methodology for reducing metals from aqueous solutions, which operates by varying the fed current and the electrolyte recirculation flow in such a way that stable operational conditions are maintained on the cathodic surface.
- aqueous solutions which operates by varying the fed current and the electrolyte recirculation flow in such a way that stable operational conditions are maintained on the cathodic surface.
- the spectrum of solutions treatable by the electro-obtaining technique is expanded to concentrations as low as 2 gpl of Cu and also, the treatment of polymetallic solutions is allowed, with the presence of As, Sb and Bi dissolved. Its use can be extended to the reduction of other metals, such as Ni, As, Zn, Ag and Co.
- the typical input concentrations of the electrolyte are 45 to 50 gpl of Cu +2 and it is discarded when it reaches 25 - 30 gpl, being sent to recharge Cu 2+ .
- the recharge of the electrolyte is carried out from a solvent extraction plant, whose function is to concentrate the Cu +2 of the solutions from leaching and not allow the passage of impurities to the electrolytic ship.
- electro-refining electrolytes with Cu +2 concentrations between 40 and 50 gpl are used, which are sent to the cleaning circuits when the Cu +2 concentrations exceed 50 gpl and / or the contents of other impurities cause the cathodic quality is jeopardized.
- the product of these operations are Copper cathodes, which have different qualities depending on the impurities present in them. It operates under normal conditions of constant cathodic current density, of the order of 250 to 380 A / m 2 and recirculation / supply flows to the cells of between 10 and 30 It / m (Fig 1).
- the voltage drop (electrical potential) in each cell varies with the depletion of the electrolyte, increasing from approximately 1.7 to 2 volts, a situation that is due to the change in the composition of the electrolyte as the process progresses.
- the harvest of the cathodes usually occurs after one week of operation, when they are removed for commercialization, replacing them with new, thin cathodes and / or mother leaves.
- the first thing that is observed is that the industrial design is oriented to a constant productive flow, given by the maintenance of the rectifier current.
- both the electrolyte and the phenomenology that appear on the cathodic surface change with the progress of the process.
- the electrolyte is depleted in Cu +2 , enriching in H + and increasing its viscosity, all phenomena that hinder the formation of Cu 0 because the presence of Cu +2 ions on the cathodic surface decreases, both due to the decrease in its concentration, like so progressively difficult to transport through the boundary layer.
- the latter occurs early on the cathodic surface (appointment 1) and defines the presence of a high cathodic polarization (qc) by concentration, a condition that increases with the advance of the shift. Then, it becomes evident that the presence of the depletion boundary layer implies:
- Fig 2 shows the results of a test in which the evolution of cathodic potential (Ec) was observed during the total decoking of a sulfuric solution, in the presence of As.
- the circuit has a remaining concentration of 0.5 g / l of Cu +2 and is charged with electrolyte with 2.5 g / l of Cu +2 .
- the system operated at constant current density and electrolyte flux. It is observed that the Ec signal increases initially (mix) and then progressively decreases to values below -580 mV / Cu-Cu +2 .
- the sequence of phenomena observed on the cathodic surface is as follows:
- H3AS gas
- electrolyte burning the phenomenon called "electrolyte burning".
- the Ec value destabilizes, abruptly decreasing and increasing its value until the almost total detachment of the CU3AS solids, which occurs at 355 minutes (zone 24).
- the stable cathodic reaction is the generation of H3AS (gas) , with stabilized Ec values below -580 mV (zone 25).
- Fig 1 represents the curve of a conventional electrowinning system in a graph showing the depletion of the Cu +2 concentration at a constant current density, with the advance of the shift. The shape of a cathodic isopotential curve El is shown.
- Fig 2 shows the evolution of the cathodic potential (Ec) during the electrolysis of a solution of 2 g / l of Cu +2 that is fed to a circuit with 0.5 g / l.
- the operation is at constant current and it is observed how the values increase during mixing, and then decrease until the generation of HsAS (gas).
- the different stages through which the cathodic reaction passes are indicated, observing that they are associated with different ranges of Ec.
- Fig 3 represents the effect of varying the electrolyte recirculation flow on the position of an Ec isopotential curve, observing effects on the current possible to apply, as well as on the Cu +2 concentrations possible to treat.
- Fig 4 shows the operation plane of the proposed new process in a graph of current density versus electrolyte recirculation flow for a given r ⁇ c polarization. It shows several Cu +2 isoconcentration curves, the operational range of recirculation flows and the circuit rectifier, in addition to four points (40, 41, 42 and 43) that define a polygon where for any interior point, they are the conditions of Cu +2 concentration, rectifier current and electrolyte flow that allow us to comply with the design r ⁇ c of the graph.
- Fig 5 shows the proposed dimensionless F values with results obtained in industrial tests. The existence of three zones of operation is observed and that the recovery of Cu ° supposes to extract no more than 6.5% of the Cu fed to the cell.
- Fig 6 shows how the cathodic quality varies as a function of the r ⁇ c polarization.
- Fig 7 shows the relationship of dimensionless F with cathodic quality, noting that for values less than 0.0025, it is possible to obtain grade A cathodes DETAILED DESCRIPTION OF THE INVENTION
- a new way of operating the reduction of dissolved metals, particularly Cu +2 to Cu °, is proposed in which the effect of the diffusion limit layer is regulated, by optimizing the variables that determine the mobilization of Cu +2 towards the cathode and the thermodynamic stability condition of the reduction reaction of Cu +2 to Cu ° (or of the metal of interest) on the cathodic surface.
- Diffusion given by Fick's law, which considers that the concentration gradient of the analyzed species defines its mobility. It assumes that the medium does not have mechanical mobility, that is, it is the predominant transport in the boundary layer.
- the thickness of the diffusion boundary layer increases, which implies that there is a direct binding relationship between the characteristics of the diffusion layer and the r ⁇ c (migratory component) .
- the r ⁇ c increases (Ec decreases) as the electrolyte recirculation flow decreases and by analogy, the r ⁇ c decreases (Ec increases), increasing the electrolyte recirculation flow in the cell.
- the r ⁇ c increases (Ec decreases) with increasing cell voltage or current flowing through it; similarly, r ⁇ c decreases by decreasing the cell voltage or the current input to the cell.
- Fig 4 shows a graph of Electrolyte flow v / si (A / m 2 ), where the plane of possible operational options with different concentrations of Cu +2 is observed, for a given cathodic potential Ec. Any point circumscribed to the polygon defined by 40-41-42 and 43 defines the flow condition, Cu +2 concentration, and operating current density to achieve the graphic design Ec. At lower Ec, the slopes of the isoconcentration curves increase, and similarly, the slopes are smaller for higher values of Ec.
- Flow partition factor which is equivalent to the fraction of the electrolyte fed to the cell that effectively circulates through the anode-cathode interface. It takes the value of 1 when all the electrolyte fed to the cells passes between anodes-cathodes (for example in a circular cell); in conventional Cu cells, it takes typical values between 0.4 and 0.7.
- F allows an indirect reading of r ⁇ c (Ec), which implies that by limiting its fluctuation, I limit r ⁇ c (Ec).
- Ec r ⁇ c
- I limit r ⁇ c (Ec) I limit r ⁇ c
- F allows the operation to be controlled by varying flows, concentrations or the current fed to the circuit, interchangeably, in order to maintain balanced transport and deposition conditions, stabilizing the phenomenology present on the cathodic surface.
- Variable Current Rectifier required to adjust the Cu +2 reduction rate according to the required Ec or F setting.
- the rectifier capacity defines a maximum current and as control elements, a warning current of low concentration of Cu +2 and a minimum operational current are defined.
- Equipment for variable supply flow equipment is required to measure and regulate the flow of electrolyte supply to each cell, according to the signals from the Ec sensors.
- the characteristics of these equipment define the maximum and minimum recirculation flows, both conditions that allow to limit the breadth of operation of the proposed methodology.
- the linear velocity of the electrolyte on the cathodic surface should not exceed 12 cm / s.
- Control PLC that from signals of Ec, fluxes, current and concentration of Cu +2 , as appropriate, acts by defining electrolyte power flows and currents fed by the rectifier, dynamically adjusting the range of Ec or operational I. Eventually, define actions associated with starting or stopping the charge of electrolyte rich in Cu +2 , turning on warning alarms for overcharging or absence of Cu +2 .
- Ec sensors in case of opting for the implementation of the methodology through Ec readings, continuously operating sensors must be installed in each cell of the circuit.
- Cu +2 sensors in case of opting for the implementation of the methodology using F, a continuously operating Cu +2 sensor must be installed in the supply to the cells.
- Fig 5 is constructed by considering plant data and reported in the bibliography. As ordinates, the value of 100 * F was exposed, in order to obtain a percentage data of the reduced Cu versus the Cu fed to the anode-cathode interface per unit of time. It is observed that for diluted Cu +2 solutions, the possibility of obtaining Cu ° at the cathode is restricted to a maximum extraction of approximately 6.5% of the Cu +2 fed to the mentioned interface (F maximum). This value decreases for solutions with a Cu +2 concentration of less than 5 gpl, and the condition must be studied on a case-by-case basis. Furthermore, it is observed that in the As values of 4 increase, the cathodic deposit can be cupro-arsenical solids and even, arsine can be generated.
- Fig 7 shows the results obtained in the operation of a circular cell and current densities less than 800 A / m 2 . It is observed that the use of values of 100 * 4 over 0.4 results in obtaining contaminated cathodes (label D) and that for values of 100 * 4 less than 0.25, grade A cathodes are obtained (label O). Then, the operation involves defining 4 in a range between 0.0020 and 0.0025, with the restriction of a maximum current density i of 800 A / m 2 . The use of values of 4 greater than 0.0025 and less than 0.0040 should be studied for each particular installation.
- Zone 61 Cu ° formation; dendritic deposits and electrolyte entrapment problems; efficient use of electrical energy fed to the circuit, but inefficient facilities; electrodes do not assure quality, it must operate with less Ec.
- Zone 62 Formation of high purity Cu ° in conventional circuits with rectangular cells and in circuits with circular cells.
- Zone 63 Formation of high purity Cu ° in circular cells; Cu ° refining in conventional rectangular cells.
- Zone 64 Refining Cu ° formation in circular cells and conventional cells.
- Zone 65 Formation of cupro-arsenical solids, of the CU 3 AS type.
- the cells must be equipped with Ec sensors, the readings of which are defined within a range within 62 for conventional cells and within 63 for circular type cells.
- electrolyte flows that mean an average speed on the cathode between 0.5 and 12 cm / s is proposed, in circular type cells.
- electrolyte channelizers the values may be lower. The ranges are referential and must be studied in consideration of each particular installation.
- Control by means of F contemplates the implementation of a Cu +2 concentration sensor in the global feed stream and of electrolyte flow sensors that feed each cell; the operation obeys the fixation of F, which implies analyzing the flow of Cu +2 that is fed to the cell (product F * [Cu] ⁇ ), which when increasing implies upward corrections of the current fed and, similarly, when decrease, decrease the rectifier current.
- Ec sensors are installed in each cell; the Ec signals will increase their value with increases in Cu +2 concentration and / or in the electrolyte flow and, similarly, they will decrease in value with decreasing Cu +2 concentration and / or electrolyte flow. Adjustments will be made only in the operation of the rectifier, which will increase or decrease the current supplied in respective response to rises or falls of Ec outside the predefined operational range.
- the rectifier will be dimensioned according to the condition of highest concentration of Cu +2 that may occur in the electrolyte, associated with the highest flow expected.
- Ec sensors are installed in the cells, which will deliver downward signals in case of Cu +2 concentration decrease and upward signals when it increases. Corrections will be to increase the electrolyte flow when Ec decreases and decrease it when Ec increases, always keeping Ec within the predefined operational range. There is also the option of supplying the circuit with a parallel current of electrolyte charged in Cu +2 , in order to increase Ec.
- the cells must be designed in conjunction with the electrolyte recirculation system, so that a maximum surface velocity of the order of 7-12 cm / s is achieved. When the maximum recirculation speed is reached, the electrolyte must be replaced by another with a higher Cu + 2 concentration.
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Electrochemistry (AREA)
- Materials Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Automation & Control Theory (AREA)
- Electrolytic Production Of Metals (AREA)
Abstract
Description
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Priority Applications (6)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US17/289,738 US20210277530A1 (en) | 2018-10-29 | 2019-10-29 | New electro-chemical process based on a dimensionless factor |
PE2021000635A PE20211765A1 (es) | 2018-10-29 | 2019-10-29 | Nuevo proceso electroquimico basado en factor adimensional |
PL437827A PL437827A1 (pl) | 2018-10-29 | 2019-10-29 | Nowy proces elektrochemiczny oparty na czynniku dodatkowym |
CA3118225A CA3118225A1 (en) | 2018-10-29 | 2019-10-29 | New electro-chemical process based on a dimensionless factor |
MX2021004911A MX2021004911A (es) | 2018-10-29 | 2019-10-29 | Nuevo proceso electroquimico basado en factor adimensional. |
AU2019373476A AU2019373476A1 (en) | 2018-10-29 | 2019-10-29 | New electro-chemical process based on a dimensionless factor |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CL3073-2018 | 2018-10-29 | ||
CL2018003073A CL2018003073A1 (es) | 2018-10-29 | 2018-10-29 | Proceso de reducción redox de metales disueltos mediante el control del potencial catódico y/o cociente adimensional, variando flujos y corrientes |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2020087189A1 true WO2020087189A1 (es) | 2020-05-07 |
Family
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Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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PCT/CL2019/050107 WO2020087189A1 (es) | 2018-10-29 | 2019-10-29 | Nuevo proceso electroquimico basado en factor adimensional |
Country Status (8)
Country | Link |
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US (1) | US20210277530A1 (es) |
AU (1) | AU2019373476A1 (es) |
CA (1) | CA3118225A1 (es) |
CL (1) | CL2018003073A1 (es) |
MX (1) | MX2021004911A (es) |
PE (1) | PE20211765A1 (es) |
PL (1) | PL437827A1 (es) |
WO (1) | WO2020087189A1 (es) |
Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
ES482203A1 (es) * | 1978-07-05 | 1980-04-01 | Cominco Ltd | Un metodo para controlar un proceso para la recuperaicon de zinc por electroextraccion. |
US4624857A (en) * | 1984-02-03 | 1986-11-25 | Schering Aktiengesellschaft | Method for automatic control of galvanic deposition of copper coatings in galvanic acid copper baths |
EP0338356A1 (de) * | 1988-04-18 | 1989-10-25 | Schering Aktiengesellschaft | Chronoamperometrische und chronopotentiometrische Messungen zur Kontrolle und Steuerung von galvanischen Kupferabscheidungen |
ES2112313T3 (es) * | 1991-02-14 | 1998-04-01 | Materials Research Pty Ltd | Aparato de recuperacion de mineral. |
WO2013057700A1 (en) * | 2011-10-19 | 2013-04-25 | Nano - Tech Sp. Z O.O. | Method of electrolytic deposition of arsenic from industrial electrolytes including waste electrolytes used in electrorefining of copper after prior decopperisation of electrolyte |
WO2013075889A1 (en) * | 2011-11-22 | 2013-05-30 | Nano-Tech Sp. Z O.O. | A method for industrial copper electrorefining |
CL2014002834A1 (es) * | 2014-10-21 | 2015-01-16 | Hecker Electronica De Potencia Y Procesos S A | Proceso de electroobtencion de cobre de alta calidad para soluciones de baja concentración de cobre y baja temperatura controlado por tensión y con aplicación de corriente alterna. |
ES2614629T3 (es) * | 2004-03-17 | 2017-06-01 | Kennecott Utah Copper Llc | Monitoreo inalámbrico de celdas electrolíticas con tensión de bus ultrabaja |
-
2018
- 2018-10-29 CL CL2018003073A patent/CL2018003073A1/es unknown
-
2019
- 2019-10-29 US US17/289,738 patent/US20210277530A1/en not_active Abandoned
- 2019-10-29 MX MX2021004911A patent/MX2021004911A/es unknown
- 2019-10-29 PE PE2021000635A patent/PE20211765A1/es unknown
- 2019-10-29 WO PCT/CL2019/050107 patent/WO2020087189A1/es active Application Filing
- 2019-10-29 CA CA3118225A patent/CA3118225A1/en not_active Abandoned
- 2019-10-29 PL PL437827A patent/PL437827A1/pl unknown
- 2019-10-29 AU AU2019373476A patent/AU2019373476A1/en active Pending
Patent Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
ES482203A1 (es) * | 1978-07-05 | 1980-04-01 | Cominco Ltd | Un metodo para controlar un proceso para la recuperaicon de zinc por electroextraccion. |
US4624857A (en) * | 1984-02-03 | 1986-11-25 | Schering Aktiengesellschaft | Method for automatic control of galvanic deposition of copper coatings in galvanic acid copper baths |
EP0338356A1 (de) * | 1988-04-18 | 1989-10-25 | Schering Aktiengesellschaft | Chronoamperometrische und chronopotentiometrische Messungen zur Kontrolle und Steuerung von galvanischen Kupferabscheidungen |
ES2112313T3 (es) * | 1991-02-14 | 1998-04-01 | Materials Research Pty Ltd | Aparato de recuperacion de mineral. |
ES2614629T3 (es) * | 2004-03-17 | 2017-06-01 | Kennecott Utah Copper Llc | Monitoreo inalámbrico de celdas electrolíticas con tensión de bus ultrabaja |
WO2013057700A1 (en) * | 2011-10-19 | 2013-04-25 | Nano - Tech Sp. Z O.O. | Method of electrolytic deposition of arsenic from industrial electrolytes including waste electrolytes used in electrorefining of copper after prior decopperisation of electrolyte |
WO2013075889A1 (en) * | 2011-11-22 | 2013-05-30 | Nano-Tech Sp. Z O.O. | A method for industrial copper electrorefining |
CL2014002834A1 (es) * | 2014-10-21 | 2015-01-16 | Hecker Electronica De Potencia Y Procesos S A | Proceso de electroobtencion de cobre de alta calidad para soluciones de baja concentración de cobre y baja temperatura controlado por tensión y con aplicación de corriente alterna. |
Non-Patent Citations (6)
Title |
---|
AWAKURA, Y. ET AL., PROFILE OF THE REFRACTIVE INDEX IN THE CATHODIC DIFFUSION LAYER OF AN ELECTROLYTE CONTAINING CUS04 AND H2SO4, vol. 124, no. 7, pages 1050 - 1057 * |
BEUKES, N. ET AL.: "Copper electrowinning: theoretical and practical design", THE JOURNAL OF THE SOUTHERN AFRICAN INSTITUTE OF MINING AND METALLURGY, vol. 109, no. 6, June 2009 (2009-06-01), pages 343 - 356, ISSN: 2411-9717 * |
GALLEGOS, A.: "Automatización de circuitos de descobrización total", 4° SEMINARIO ACERCAMIENTO TECNOLÓGICO, 2008, Retrieved from the Internet <URL:https://www.codelco.com/flipbook/innovacion/codelcodigital4/dia2.htm> [retrieved on 20190812] * |
IBANEZ, J. ET AL.: "Modelación del transporte de cobre en la capa limite en una celda de electrodialisis", REVISTA DE METALURGIA, vol. 40, no. 2, 2004 * |
LOS, P. ET AL.: "Laboratory and Pilot Scale Tests of a New Potential-Controlled Method of Copper Industrial Electrolysis", JOURNAL OF THE ELECTROCHEMICAL SOCIETY, vol. 161, no. 10, 2014, pages D593 - D599, XP055706895 * |
WERNER ET AL.: "Modeling and validation of local electrowinning electrode current density using two phase flow and Nernst-Planck equations", JOURNAL OF THE ELECTROCHEMICAL SOCIETY, vol. 165, no. 5, January 2018 (2018-01-01), pages E190 - E207, XP055706900 * |
Also Published As
Publication number | Publication date |
---|---|
PE20211765A1 (es) | 2021-09-07 |
MX2021004911A (es) | 2021-06-18 |
CA3118225A1 (en) | 2020-05-07 |
CL2018003073A1 (es) | 2018-11-30 |
PL437827A1 (pl) | 2021-11-29 |
US20210277530A1 (en) | 2021-09-09 |
AU2019373476A1 (en) | 2021-06-10 |
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