This application is a U.S. National Phase Application under 35 U.S.C. §371 of International Patent Application No. PCT/IN2012/000486 filed Jul. 9, 2012, which claims the benefit of Indian Patent Application Serial No. 1975/MUM/2011 filed Jul. 8, 2011, both of which are incorporated herein by reference in their entirety.
The present invention related to tubular electrochemical cell for electrolysis of cuprous chloride to copper powder and cupric chloride. The material used for fabrication of cell is dense graphite tube as anode and dense copper rod as cathode, separated by ion exchange membrane supported by acrylic tube. Electrochemical cell of invention can be used for recovery of metals such as silver, zinc and lead from their salt solutions.
Many industries like plating, mining and metal finishing were also using electrolysis to recover metal from the electrolyte. Recovery of copper from the solutions containing copper metal in the form of ions is well known process. In CuCl cycle the copper consume in hydrogen production step is reproduced in the cathode side of electrolysis. The cupric chloride formed in the anode side was used as starting material for hydrolysis of cupric chloride and decomposition of cupric chloride.
U.S. Ser. No. 00/542,1966A used the electrolysis process for regeneration of acid cupric chloride etching bath to recover copper metal. The applicant used graphite rod as anode and cathode electrodes. Micro porous separator was used for separation of anolyte and catholyte solution.
US20080283390A1 describer a method for electrolysis of cuprous chloride to produce copper powder and cupric chloride. Dense graphite was used as working electrodes as anode and cathode. Anion exchange membrane made up from poly and polyethylenimine cross-linked is used as a separating medium. The electrodes are designed in the form of channels rib manner. The electrolyte flows through the respective channels. The main problem faced is the removal of copper powder formed during the electrolysis. The applicants have used different additives to enhance the solubility of CuCl. To increase the conductivity of solution was seeded with carbon black material.
US2010051469A1 used electrochemical cell for production of hydrogen gas and cupric chloride from the electrolysis of cuprous chloride. The anolyte and catholyte used were cuprous chloride in hydrochloric acid and water respectively. Cation exchange membrane was used as separating medium between the anode and cathode compartment.
One of the objectives of the present invention is to design the electrochemical cell for electrolysis of cuprous chloride using acid resistant material to get required size of copper powder.
Another objective of the present invention is recovery of metals such as silver, zinc and lead from their salt solutions.
Another objective of the present invention is to achieve desired particle of metal which is to be recovered.
Another objective of the present invention is to design an electrochemical cell with anode and cathode with effective surface area for desired metal particle.
A thermochemical Cu—Cl thermochemical cycle consists of six steps: (1) hydrogen production; (2) electrolysis of cuprous chloride; (3) drying of cupric chloride; (4) hydrolysis of cupric chloride; (5) decomposition of cupric chloride and (6) oxygen production step. Using tubular/cylindrical electrochemical cell of invention copper is produced.
The present electrochemical cell for recovery of metals comprises of
The electrochemical cell of this invention is capable of recovering metals such as copper, silver, zinc, and lead from their salt solutions at either high or very low concentrations.
In accordance with one aspect of present invention, there is provided an electrochemical cell for production of copper from cuprous chloride generated in Copper-Chlorine (Cu—Cl) thermochemical cycle.
The high surface area ratio of anode to cathode gives maximum cathodic current density providing fine and uniform particle size.
Embodiments of the inventions will be described in conjunction with the accompanying drawing, wherein;
The invention relates about electrolysis of cuprous chloride to copper powder on cathodic side and formation of cupric chloride on anodic side of the cell. By implementing the invention it is possible to electrolyze cuprous chloride and effectively removes and recovers the copper powder formed during the electrolysis. The electrolysis cell is made using tubular graphite anode and copper rod separated by ion exchange membrane supported by acrylic cylinders.
Using tubular electrochemical cell of invention copper is produced. Similarly same tubular/cylindrical electrochemical cell can be used for other metals like silver, zinc and lead.
By implementing the invention it is possible to recover metal effectively by electrochemical cell of present invention wherein electrolysis of electrolyte to recover metal is carried out. The electrolysis cell is made up of using graphite cylinder and copper rod separated by an ion exchange membrane supported by acid resistant material.
As elaborated in detail below, the main problems in the electrolysis of cuprous chloride like removal of copper powder deposited on cathode, obtaining the desired size of the copper powder in continuous operation, removal of copper powder from the closed loop and scale up of the electrolyte cell are solved by implementing the present invention.
An electrochemical cell of invention for recovery of metals comprising of at least one anode disposed in electrolyte; at least one cathode disposed in electrolyte; at least one ion exchange membrane disposed between the anode compartment and the cathode compartment a corrosion resistant material support to ion exchange membrane; at least one scraper to remove deposited metal from the cathode and at least one catholyte trapper collects scraped metal powder.
The invention deals with closed loop electrochemical cell 1 used for the electrolysis of cuprous chloride is shown in
In accordance with present invention anode 2 is constructed of dense open ended graphite cylinder as shown in
In accordance to the invention, the distance between anode and cathode may be varied by changing the inner diameter of the graphite tube/cylinder and outer diameter of copper rod. The separation of anolyte and catholyte is done using an anion exchange membrane 4 having support of acrylic cylinder 5 (shown in
In this invention for the passage of ions between anolyte and catholyte, the holes are made on the surface of the acrylic cylinder which acts as a support to the anion exchange membrane. The diameter of acrylic cylinder used in electrolysis is slightly small than the half the inner diameter of graphite tube/cylinder used as anode. Thus a cathode is placed coaxial and at the center of an anode.
In this invention, graphite cylinder and acrylic cylinders are of similar length. The first open ends of the graphite cylinder and acrylic cylinders are packed with the help of first end caps 6 and second open ends of the graphite cylinder and acrylic cylinders are packed with second end cap 7. The second end cap shown in
The top view of first teflon gasket and second teflon gasket is shown in
The power supply is provided by means of rectifier 18. The required quantity of current is passed through the electrolyte. The positive end of rectifier connected to the graphite tube/cylinder which acts as anode and negative end connected to copper rod which acts as cathode.
The first end and second end of the cell are kept intact using nut bolt 20 as shown in
Thus one of the embodiment of the invention is that anode can be composed of corrosion resistant conductive metals, conductive carbon material and any non-conductive material coated by conductive materials. Further an anode can be graphite but an anode is hollow.
One of the embodiment of the present invention is that a cathode can be composed of corrosion resistant conductive metals, conductive carbon material and any non conductive material coated by conductive materials. Thus cathode can be copper and of any geometry by keeping both ends of an anode open.
Anode and cathode have surface area in the ratio of range of 1:1 to 1:50; most preferably in the range of 1:6 to 1:15.
It is found that support is made of corrosion resistant and non conductive material and can be selected from a ceramic, thermoplastic or thermoset polymeric material.
Another embodiment of the invention is that support in electrochemical cell is provided with openings for ion transport from anolyte to catholyte wherein these openings on the support can be of any geometry. But for present invention these openings on the support are of any size and uniformly distributed area having area covered in the range of 10% to 95% of total area of support.
One of the embodiment of the invention id that scraper provided to cathode and composed of corrosion resistant and non conductive material. Scraper can be composed of a ceramic, thermoplastic or thermoset polymeric material.
An electrochemical cell according to present invention wherein anode and cathode are partially coated with corrosion resistant and non conductive material.
One of the embodiment of the present invention is that cathode is partially coated with corrosion resistant and non conductive material.
One of the embodiments of the present invention is that anode is partially coated with corrosion resistant and non conductive material.
One of the embodiments of the present invention is that cathode is partially coated with non conductive material and/or cathode can be partially coated with non conductive material at least in one plane.
In this invention, during the operation the electrolyte is passed in a close loop system. With the passage current for particular interval of time, copper get deposited on the cathode surface in the form of powder. Current is stopped for fraction of time and deposited copper is removed by use of mechanical scrubber 19 (
While the invention has been described in terms of exemplary embodiments, those skilled in the art will recognize that the invention can be practical with modification and in the spirit and scope of applied claims.
According to the present invention, the experiments of recovery of copper metal by electrolysis of cuprous chloride were carried out in the above mentioned electrochemical cell using cuprous chloride in hydrochloric acid as electrolyte. The electrolyte was pumped through their respective compartments using peristaltic pump.
Recovery of copper metal from cuprous chloride was carried out at room temperature by applying 100 mA/cm2 cathodic current density. The scaning electron microscopy (SEM) image obtained for copper metal formed during electrolysis is shown in
According to the present invention, the experiments of recovery of silver metal by electrolysis of silver nitrate were carried out in the above mentioned electrochemical cell using silver nitrate in nitric acid as electrolyte. The electrolyte was pumped through their respective compartments using peristaltic pump.
Recovery of silver metal from silver nitrate was carried out at room temperature by applying 60 mA/cm2 cathodic current density. The scaning electron microscopy (SEM) image obtained for silver metal formed during electrolysis is shown in
According to the present invention, the experiments of recovery of zinc metal by electrolysis of zinc nitrate were carried out in the above mentioned electrochemical cell using zinc nitrate in nitric acid as electrolyte. The electrolyte was pumped through their respective compartments using peristaltic pump.
Recovery of zinc metal from zinc nitrate was carried out at room temperature by applying 100 mA/cm2 cathodic current density. The scaning electron microscopy (SEM) image obtained for zinc metal formed during electrolysis is shown in
According to the present invention, the experiments of recovery of lead metal by electrolysis of lead nitrate were carried out in the above mentioned electrochemical cell using zinc nitrate in nitric acid as electrolyte. The electrolyte was pumped through their respective compartments using peristaltic pump.
Recovery of lead metal from zinc nitrate was carried out at room temperature by applying 100 mA/cm2 cathodic current density. The scaning electron microscopy (SEM) image obtained for lead metal formed during electrolysis is shown in
Number | Date | Country | Kind |
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1975/MUM/2011 | Jul 2011 | IN | national |
Filing Document | Filing Date | Country | Kind | 371c Date |
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PCT/IN2012/000486 | 7/9/2012 | WO | 00 | 4/28/2014 |
Publishing Document | Publishing Date | Country | Kind |
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WO2013/054342 | 4/18/2013 | WO | A |
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Entry |
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International Search Report issued in PCT/IN2012/000486, mailed Jun. 26, 2013, 4 pages. |
Number | Date | Country | |
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20140246307 A1 | Sep 2014 | US |