Patent Application
20220145484
The present invention relates to a method of electrochemically reducing multiple metal oxide pellets simultaneously. The present invention also provides an electrochemical cell for electrochemically reducing multiple metal oxide pellets simultaneously.
Electrochemical reduction of metals is commonly known in the art. In particular, electrolytic processes may be used, for example, to reduce metal compounds or semi-metal compounds to metals, semi-metals, or partially-reduced compounds, or to reduce mixtures of metal compounds to form alloys.
There has been great interest in the direct production of metal by direct reduction of a solid metal oxide feedstock. However, the problem with the prior art methods is that the methods are a low-throughput synthesis of metals since only one metal oxide can be processed at a time.
Thus, there is a need for an improved method of producing metal.
The present invention seeks to address these problems, and/or to provide a method for simultaneously electrochemically reducing multiple metal oxide pellets to enable efficient production of metals at high throughput. The present invention also provides an electrochemical cell suitable for simultaneously electrochemically reducing multiple metal oxide pellets.
According to a first aspect, the present invention provides a method of electrochemically reducing multiple metal oxide pellets simultaneously, the method comprising:
According to a particular aspect, each of the multiple metal oxide pellets may have the same or different composition from each other.
Each of the multiple metal oxide pellets may comprise at least one metal oxide. The at least one metal oxide may be an oxide of any suitable metal. For example, the at least one metal oxide may be, but not limited to: titanium oxide (TiO2), cobalt oxide (CoO), chromium oxide (Cr2O3), iron oxide (Fe2O3), nickel oxide (NiO), aluminium oxide (Al2O3), manganese oxide (MnO2), niobium pentoxide (Nb2O5), tin (IV) oxide (SnO2), tantalum pentoxide (Ta2O5), terbium (III) oxide (Tb2O3), lanthanum oxide (La2O3), zirconium dioxide (ZrO2), silicon dioxide (SiO2), vanadium pentoxide (V2O5), vanadium dioxide (VO2), vanadium trioxide (V2O3), ytterbium oxide (Yb2O3), dysprosium oxide (Dy2O3), erbium oxide (Er2O3), samarium oxide (Sm2O3) gadolinium oxide (Gd2O3), germanium dioxide (GeO2), magnesium oxide (MgO), neodymium oxide (Nd2O3), lithium superoxide (LiO2), cerium oxide (CeO2), copper oxide (CuO), uranium dioxide (UO2), triuranium octoxide (U3O8), hafnium dioxide (HfO2), tungsten trioxide (WO3), NiAl2O4, SrTiO3, FeTiO3, CaWO4, or a combination thereof.
According to a particular aspect, each of the multiple metal oxide pellets may be porous. For example, each of the multiple metal oxide pellets may have a porosity of 5-60%.
Each of the multiple metal oxide pellets may be of any suitable size and shape. For example, the pellet may have an average size of 2-100 mm.
The cathode may be any suitable cathode. For example, the cathode may comprise, but is not limited to, titanium (Ti), stainless steel, molybdenum, nickel, iron-chromium-aluminium (FeCrAl) alloy, or a combination thereof.
The anode may be any suitable anode. For example, the anode may comprise, but is not limited to, graphite, glassy carbon, CaRuO3, SnO2, or a combination thereof.
The electrolyte may be any suitable electrolyte for the purposes of the present invention. According to a particular aspect, the electrolyte may comprise a molten salt. The molten salt may be any suitable molten salt. For example, the molten salt may be, but not limited to, calcium chloride (CaCl2), lithium chloride (LiCl), lithium oxide (Li2O), sodium chloride (NaCl), calcium oxide (CaO), lithium bromide (LiBr), potassium bromide (KBr), cesium bromide (CsBr), calcium bromide (CaBr2), potassium chloride (KCl), potassium bromide (KBr), or a combination thereof.
According to a particular aspect, the electrolyte may be in a molten state. Accordingly, the method may further comprise heating the electrolyte prior to the contacting. In particular, the heating may comprise melting the electrolyte to a molten state. The electrolyte may be at any suitable temperature. For example, the electrolyte may be at a temperature of 400-1200° C. prior to the contacting.
The method may be carried out under an inert atmosphere. For example, the inert atmosphere may comprise, but is not limited to, argon.
The applying may be for a suitable period of time. According to a particular aspect, the applying may be for a pre-determined period of time.
The method may further comprise collecting the multiple metal oxide pellets following the applying to recover the metals.
According to a second aspect, the present invention provides an electrochemical cell for electrochemically reducing multiple metal oxide pellets simultaneously, the cell comprising:
The anode, cathode and electrolyte may be any suitable anode, cathode and electrolyte, respectively. In particular, the anode, cathode and electrolyte may be as described above in relation to the first aspect.
Each of the multiple metal oxide pellets may be any suitable metal oxide pellet. In particular, each of the multiple metal oxide pellets may be as described above in relation to the first aspect.
In order that the invention may be fully understood and readily put into practical effect there shall now be described by way of non-limitative example only exemplary embodiments, the description being with reference to the accompanying illustrative drawings. In the drawings:
As explained above, there is a need for an improved method of producing metal.
In general terms, the present invention provides an efficient production of metals at high-throughput. This provides several advantages such as reducing lead time for material discovery, as well as providing a more practical way of scaling up production of metals. The method of the present invention may also be suitable for producing metal alloys by reducing multiple elemental compositions. The present invention also provides an electrochemical cell to efficiently produce the metals.
According to a first aspect, the present invention provides a method of electrochemically reducing multiple metal oxide pellets simultaneously, the method comprising:
contacting an anode and a cathode with multiple metal oxide pellets with an electrolyte, wherein the multiple metal oxide pellets are secured to the cathode; and
For the purposes of the present invention, the term metal may be defined to encompass all such products, such as metals, semi-metals, alloys, intermetallics. Metal may also be considered, where appropriate, to include partially reduced products.
According to a particular aspect, each of the multiple metal oxide pellets may have the same or different composition from each other. According to a particular embodiment, each of the multiple metal oxide pellets may be the same as each other. According to another particular embodiment, each of the multiple metal oxide pellets may be different from each other. According to yet another embodiment, some of metal oxide pellets may be the same while other within the multiple metal oxide pellets may be different.
Each of the multiple metal oxide pellets may comprise at least one metal oxide. The at least one metal oxide may be an oxide of any suitable metal. For example, the at least one metal oxide may be, but not limited to: titanium oxide (TiO2), cobalt oxide (CoO), chromium oxide (Cr2O3), iron oxide (Fe2O3), nickel oxide (NiO), aluminium oxide (Al2O3), manganese oxide (MnO2), niobium pentoxide (Nb2O5), tin (IV) oxide (SnO2), tantalum pentoxide (Ta2O5), terbium (III) oxide (Tb2O3), lanthanum oxide (La2O3), zirconium dioxide (ZrO2), silicon dioxide (SiO2), vanadium pentoxide (V2O5), vanadium dioxide (VO2), vanadium trioxide (V2O3), ytterbium oxide (Yb2O3), dysprosium oxide (Dy2O3) erbium oxide (Er2O3), samarium oxide (Sm2O3) gadolinium oxide (Gd2O3), germanium dioxide (GeO2), magnesium oxide (MgO), neodymium oxide (Nd2O3), lithium superoxide (LiO2), cerium oxide (CeO2), copper oxide (CuO), uranium dioxide (UO2), triuranium octoxide (U3O8), hafnium dioxide (HfO2), tungsten trioxide (WO3), NiAl2O4, SrTiO3, FeTiO3, CaWO4, or a combination thereof.
According to a particular aspect, the multiple metal oxide pellets may comprise at least one pellet comprising TiO2, at least one pellet comprising CoO, Cr2O3, Fe2O3 and NiO, and/or at least one pellet comprising Al2O3, CoO, Cr2O3, Fe2O3 and NiO.
The method of the present invention may be suitable for forming any metal or its alloy. For example, the method may be for reducing metal oxides comprised in the multiple metal oxide pellets to form titanium (Ti), cobalt (Co), chromium (Cr), iron (Fe), nickel (Ni), aluminium (Al), or an alloy thereof. In particular, the method may be for forming at least one of Ti, CoCrFeNi or AlxCoCrFeNi, wherein x is 0.1 to 2.0.
For example, when it is desired to form pure Ti, the multiple metal oxide pellets may comprise TiO2. When it is desired to form high entropy alloy CoCrFeNi, the multiple metal oxide pellets may comprise CoO, Cr2O3, Fe2O3 and NiO. When it is desired to form high entropy alloy AlxCoCrFeNi, the multiple metal oxide pellets may comprise Al2O3, CoO, Cr2O3, Fe2O3 and NiO.
According to a particular aspect, each of the multiple metal oxide pellets may be porous. If the pellets are too porous, they may not be mechanically strong enough to withstand handling and would crumble into the electrolyte during the electrochemical reduction of the pellet. On the other hand, if the pellets are not porous enough, the electrochemical reduction process would be very slow. Accordingly, each of the multiple metal oxide pellets may have a suitable porosity. For example, each of the multiple metal oxide pellets may have a porosity of 5-60%. In particular, the porosity may be 10-56%, 15-55%, 20-50%, 25-48%, 30-45%, 35-40%. Even more in particular, the porosity may be 45-60%.
Each of the multiple metal oxide pellets may be of any suitable size and shape. For the purposes of the present invention, a pellet may be defined as a compressed metal oxide having any suitable size and shape, wherein the pellet may comprise at least one metal oxide.
Examples of suitable shapes of the pellets may include, but is not limited to, annular, spherical, elliptical, cubic, pyramidal, cylindrical. In particular, the pellet may be annular.
The pellet may have an average size of 2-100 mm. For the purposes of the present invention, average size may refer to at least one of the height, width, or diameter of the pellet. In particular, the pellet may have an average size of 5-90 mm, 10-85 mm, 15-80 mm, 20-75 mm, 25-70 mm, 30-65 mm, 35-60 mm, 40-55 mm, 45-50 mm. Even more in particular, the pellet may have an average size of 10-20 mm.
According to a particular embodiment, the pellet may be annular having an outer diameter of about 15 mm, an inner diameter of about 5 mm and a thickness of about 3-3.5 mm.
The multiple metal oxide pellets may be prepared by any suitable method. For example, the preparing of the metal oxide pellets may comprise sintering each of the multiple metal oxide pellets. The sintering may be by any suitable method. The advantage of this is that the pellets are able to maintain structural integrity so that the pellet does not fall apart before or during the electrochemical reduction of the pellet.
Each of the multiple metal oxide pellets may be secured to the cathode by any suitable manner. The pellets may be secured to the cathode to ensure that the metal oxide pellets are in constant electrical contact with the cathode at all times during the method.
According to a particular aspect, the cathode may be screw-threaded so that each of the multiple metal oxide pellets may be secured to the cathode by a nut at the cathode. In this way, the pellets are prevented from dropping into the electrolyte and this also enables the surface area of the pellets in contact with the cathode to increase. Further, each of the multiple metal oxide pellets may be separated from one another by any suitable means. For example, the pellets may be separated by using a small segment of wire, such as, but not limited to, iron-chromium-aluminium (FeCrAl) alloy wire.
The multiple metal oxide pellets may be further secured by a wire cage so that the pellets are prevented from falling off the cathode in case the pellets crack during the method. The wire cage may be of any suitable material. For example, the wire cage may be of FeCrAl alloy wire.
The cathode may be any suitable cathode. For example, the cathode may comprise, but is not limited to, titanium (Ti), stainless steel, molybdenum, nickel, iron-chromium-aluminium (FeCrAl) alloy, or a combination thereof.
The anode may be any suitable anode. For example, the anode may comprise, but is not limited to, graphite, glassy carbon, CaRuO3, SnO2, or a combination thereof. In particular, when carbon based anodes are used, carbon dioxide may be evolved at the anode during the electrochemical reduction. When inert anodes, such as CaRuO3, SnO2 are used, oxygen may be evolved at the anode during the electrochemical reduction.
The electrolyte may be any suitable electrolyte for the purposes of the present invention. According to a particular aspect, the electrolyte may comprise a molten salt. The molten salt may be any suitable molten salt to facilitate reduction of the multiple metal oxide pellets. For example, the molten salt may comprise an alkali halide salt, an alkaline earth metal halide salt, an alkali oxide, or combinations thereof. In particular, the molten salt may comprise, but is not limited to, lithium chloride (LiCl), lithium oxide (Li2O), sodium chloride (NaCl), calcium chloride (CaCl2), calcium oxide (CaO), lithium bromide (LiBr), potassium bromide (KBr), cesium bromide (CsBr), calcium bromide (CaBr2), potassium chloride (KCl), potassium bromide (KBr), or a combination thereof. Even more in particular, the molten salt may be CaCl2 or a combination of CaCl2 and CaO.
According to a particular aspect, the electrolyte may comprise a molten salt and an additive. The additive may be any suitable additive. For example, the additive may be an alkali earth metal oxide. In particular, the additive may be CaO.
The additive may be added in any suitable amount. For example, the additive may be added at a weight concentration of 0.25-5.0 weight % of the electrolyte. In particular, the additive may be added at a weight concentration of 0.5-4.5 wt %, 1.0-4.0 wt %, 1.5-3.5 wt %, 2.0-3.0 wt %, 2.5-2.8 wt % of the electrolyte. Even more in particular, the additive may be added at a weight concentration of 0.1-1.0 wt % of the electrolyte.
According to a particular embodiment, the electrolyte may comprise CaCl2 and CaO. The CaO may constitute 0.25-5.0 weight % of the electrolyte. In particular, the CaO may constitute 0.5-4.5 wt %, 1.0-4.0 wt %, 1.5-3.5 wt %, 2.0-3.0 wt %, 2.5-2.8 wt % of the electrolyte. The CaCl2 may constitute the remainder of the electrolyte. Even more in particular, the electrolyte may comprise 2.0 wt % CaO.
According to a particular aspect, the electrolyte may be in a molten state during the method. Accordingly, the method may further comprise heating the electrolyte prior to the contacting. The heating may be by any suitable means. In particular, the heating may comprise melting the electrolyte to a molten state. The electrolyte may remain in the molten state during the method. Therefore, the temperature of the electrolyte may be maintained at or above a melting temperature of the molten salt comprised in the electrolyte. The electrolyte may be at any suitable temperature. For example, the electrolyte may be at a temperature of 400-1200° C. prior to the contacting. In particular, the temperature may be 420-1150° C., 450-1100° C., 500-1000° C., 550-950° C., 600-900° C., 650-850° C., 700-800° C. Even more in particular, the temperature may be about 900° C.
The method may be carried out under an inert atmosphere. For example, the inert atmosphere may comprise an inert gas such as, but not limited to, argon, helium, or a combination thereof. In particular, the inert atmosphere may comprise argon.
The applying an electrical potential between the anode and the cathode may be by any suitable means. For example, the electrical potential may be applied by, but not limited to, a DC power supply.
The applying may be for a suitable period of time. According to a particular aspect, the applying may be for a pre-determined period of time. For example, the pre-determined period of time may be 6-48 hours. In particular, the pre-determined period of time may be 12-45 hours, 18-42 hours, 24-36 hours, 30-32 hours. Even more in particular, the pre-determined period of time may be about 24 hours.
The applying results in a provision of a polarization field and a driving force for moving oxide ions dissolved from the metal oxide pellet at the cathode to the anode, facilitating reduction of the metal oxide at the cathode.
In particular, the electrolyte may facilitate reduction of the metal oxide pellets. For example, the metal oxide pellets may be reduced at the cathode, according to Equation (1) below:
MyOx+ze−→yM+z/xO2 (1),
wherein M is a metal, MA is the metal oxide, x is the stoichiometric amount of oxygen for the particular metal oxide, y is the stoichiometric amount of the metal in the metal oxide, and z is the stoichiometric amount of electrons for balancing the chemical reaction. The electrons are provided by applying an electrical potential between the anode and the cathode. The composition of the metal formed at the cathode may vary based on the composition of the metal oxide pellets.
The oxide ions generated at the cathode may be transported from the cathode to the anode responsive to exposure to the applied electrical field. The oxide ions may be oxidized at the anode according to Equation (2) below:
2O2−→O2(g)+4e− (2).
The oxygen gas generated at the anode may be evolved at the anode. The electrons may be returned to the anode surface.
The method may further comprise collecting the pellets following the applying to recover the metals. The recovering of the metals from the pellets may be by any suitable method. For example, the pellets may be cleaned using suitable solvents and dried to obtain the metal. The solvents may be, but not limited to, hydrochloric acid (HCl), distilled water, or a combination thereof. The pellets may be dried by any suitable means. For example, the pellets may be dried in an oven at a suitable temperature such as, but not limited to, 100° C.
According to a particular aspect, the method may comprise a pre-electrolysis prior to the electrochemical reduction of the metal oxide pellets. The pre-electrolysis comprises applying an electrical potential between the anode and a pre-electrolysis cathode. The pre-electrolysis cathode may be any suitable cathode which does not comprise any metal oxide pellets. The pre-electrolysis may eliminate any trace amounts of impurities which may be present in the electrolyte. The pre-electrolysis may be carried out for a suitable period of time.
According to a second aspect, the present invention provides an electrochemical cell for electrochemically reducing multiple metal oxide pellets simultaneously, the cell comprising:
The anode, cathode and electrolyte may be any suitable anode, cathode and electrolyte, respectively. In particular, the anode, cathode and electrolyte may be as described above in relation to the first aspect.
Each of the multiple metal oxide pellets may be any suitable metal oxide pellet. In particular, each of the multiple metal oxide pellets may be as described above in relation to the first aspect.
A schematic representation of the cell according to an embodiment of the present invention is shown in
Each of the metal oxide pellets 108a, 108b and 108c may be separated from each other as shown in
The electrochemical cell 100 may optionally be contained within a gas-tight enclosure 116, which may include a gas inlet 118 and a gas outlet 120. The gas-tight enclosure 116 may be made gas-tight by providing an O-ring 117 for sealing the enclosure 116. However, any other suitable sealing means may be used for sealing the enclosure 116.
The gas inlet 118 may be configured for providing, for example, a gas to the enclosure 116 for maintaining a gas pressure within the enclosure 116. Gases may be removed from the enclosure 116 via the gas outlet 120. The gas may comprise an inert gas, such as that described above.
The enclosure 116 may further include heating means 122 for heating or maintaining a temperature of the molten salt electrolyte 106 in the electrochemical cell 102. The heating means 122 may be any suitable heating means such as, but not limited to, a heater, a heating element, or a combination thereof.
The molten salt electrolyte 106 may be comprised in a crucible 124. The crucible 124 may be any suitable crucible. For example, the crucible 124 may be formed of a metal, glassy carbon, ceramic, a metal alloy, or any other suitable material. The crucible 124 may also be formed of a non-metallic material, such as alumina (Al2O3), magnesia (MgO), glassy carbon, graphite, boron nitride, or combinations thereof. In particular, the crucible 124 may be formed from any suitable insulating refractory material. Even more in particular, the crucible 124 may be formed of alumina.
As noted above, molten salt electrolyte 106 may be disposed in the crucible 124, in which the anode 102 and the cathode 104 are also located. In some embodiments, the electrochemical cell 100 may further comprise a pre-electrolysis cathode 104a located in crucible 124 and configured for removing impurities in the electrolyte 106. The pre-electrolysis cathode 104a does not comprise any metal oxide pellets. The pre-electrolysis cathode 104a may be lifted out of the electrolyte 106 prior to the electrochemical reduction of metal oxide pellets. In particular, the system of
The electrochemical cell 100 may further comprise connections 126 to a power supply. The power supply may be any suitable power supply such as a DC power supply. The connections 126 may be electrically coupled to each of the anode 102, the cathode 104, and the pre-electrolysis cathode 104a. The connections 126 may be configured to provide an electric potential between the anode 102 and the cathode 104, and between the anode 102 and the pre-electrolysis cathode 104a. The difference between the electric potential of the anode 102 and the electric potential of the cathode 104 may be referred to as a cell potential of the electrochemical cell 100.
The electric potential applied between the anode 102 and the cathode 104 may deposit at least one metal by reduction of the metal oxide pellets 108a, 108b and 108c simultaneously since all the metal oxide pellets 108a, 108b and 108c are provided on the cathode 104.
The electrochemical cell 100 may further comprise a cooling inlet 128 and a cooling outlet 130. The cooling inlet 128 and the cooling outlet 130 may be used for passing cooling liquid around the electrochemical cell 102 to cool down the electrochemical cell 102 following electrochemical reduction of the metal oxide pellets 108a, 108b and 108c and/or for maintaining the temperature of the molten salt electrolyte 106 during the electrochemical reduction method. The cooling liquid may be any suitable liquid. For example, the cooling liquid may be water.
Having now generally described the invention, the same will be more readily understood through reference to the following embodiment which is provided by way of illustration, and is not intended to be limiting.
5% poly(vinyl butyral) (molecular weight 30000-35000, Arcos Organics) was dissolved in isopropanol and added to TiO2 powder (40982-08, Kanto Chemical Co Inc.). The mixture was ground in a mortar until dry and sieved. 1 g of the resultant mixture was uniaxially pressed at 25-100 MPa in a hollow die and sintered at 900° C. in air for 2 hours. The resultant pellet had an outer diameter of 15 mm and 5 mm inner diameter with a thickness of about 3-3.5 mm. The porosity of the pellets varied between 48-56%.
The pellets were then secured to a cathode to ensure that the pellets were in constant electrical contact with the cathode. The cathode was screw-threaded and the pellets were secured onto the cathode by a metal nut at the end of the cathode. In this way, the pellets were prevented from dropping into the electrolyte when the cathode is placed in an electrolyte. This also resulted in an increase in the surface area of the pellets in contact with the cathode due to the enhanced contact with the metal nut. Each pellet was separated from the next pellet by a small segment of iron-chromium-aluminium (FeCrAl) alloy wire (Kanthal wire) or metal nut. The pellets were further secured by a cage of iron-chromium-aluminium (FeCrAl) alloy wire to prevent the pellets from falling off the cathode in case the pellets cracked during the electrochemical reduction method.
Preparation of CaCl2 electrolyte with 2 mol % CaO 213 g of anhydrous calcium chloride (746495, Sigma-Aldrich) and 2.3 g (2 mol %) of CaO (208159 Sigma-Aldrich) was mixed and added into an alumina crucible. The alumina crucible was placed in a vacuum oven and dried at 120° C. under vacuum overnight.
The electrochemical reduction was performed in an electrochemical cell as shown in
Following that, the pre-electrolysis cathode was lifted up and the Ti cathode with the metal oxide pellets was lowered into the electrolyte. The electrolysis was performed at 3.2 V for about 24 hours. After the reaction had completed, the electrodes were lifted up and the setup was allowed to cool to room temperature.
The pellets were detached from the cathode and thoroughly rinsed with tap water and then cleaned with dilute hydrochloric acid and distilled water. The pellets were then dried in a vacuum oven at 100° C.
Preparation of Mixed Oxide Pellets Containing CoO, Cr2O3, Fe2O3 and NiO
Cobalt oxide, chromium oxide, iron oxide and nickel oxide were ball milled with a ball-power-ratio of 18 at 200 rpm for 5 hours (molar ratio 1:1:1:1). Pre-determined molar 1% by mass of PVA and 0.5% by mass of PEG (M.W. 14000) was then dissolved in isopropanol and added to the mixture. The mixture was ground in a mortar until dry. 1 g of the resultant mixture was uniaxially pressed at 25-100 MPa in a hollow die and sintered at 900° C. in air for 2 hours. The resultant pellet had an outer diameter of about 15 mm an inner diameter of about 5 mm with a thickness of about 3-3.5 mm.
Loading the Pellet onto the Electrochemical Reactor
The cathode was screw-threaded and the pellets were secured onto the cathode by a metal nut at the end of the cathode to prevent the pellets from dropping into the electrolyte and to also increase the surface area in contact with the cathode due to the enhanced contact with the metal nut. Each pellet was then separated from the next pellet by a metal nut. The pellets were secured again by a cage of Kanthal wire to prevent the pellets from falling off the cathode in case the pellets cracked.
180 g of anhydrous calcium chloride (746495, Sigma-Aldrich) was added to an alumina crucible and placed in a vacuum oven and dried at 200° C. under vacuum overnight.
The electrochemical reduction was carried out similarly to that as described in Example 1, except that pre-electrolysis was carried out at a DC power supply of 2.8 V. Thereafter, electrolysis was performed at 3.0 V over 24 hours.
After the reaction had completed, the electrodes were lifted up and the setup was allowed to cool to room temperature. The pellets were thoroughly rinsed with DI water and acetone, and then dried in a vacuum oven at 60° C.
XRD analysis of the final product showed that the metal oxide pellets were successfully reduced.
Preparation of Mixed Oxide Pellets Containing Al2O3, CoO, Cr2O3, Fe2O3 and NiO
Aluminium oxide, cobalt oxide, chromium oxide, iron oxide and nickel oxide were ball milled with a ball-power-ratio of 18 at 200 rpm for 5 hours (molar ratio x:1:1:1:1, where x=0.1-2.0). Pre-determined molar 1% by mass of PVA and 0.5% by mass of PEG (M.W. 14000) was then dissolved in isopropanol and added to the mixture. The mixture was ground in a mortar until dry. 1 g of the resultant mixture was uniaxially pressed at 25-100 MPa in a hollow die and sintered at 900° C. in air for 2 hours. The resultant pellet had an outer diameter of about 15 mm an inner diameter of about 5 mm with a thickness of about 3-3.5 mm.
Loading the Pellet onto the Electrochemical Reactor
The pellets were secured onto the cathode in the same manner as had been done in Example 2.
The electrolyte was prepared in the same manner as in Example 2.
The electrochemical reduction was carried out in the same manner as described in Example 2. Thereafter, the pellets were collected and cleaned as described in Example 2.
The pellets were then crushed into powder and sintered using spark plasma sintering to consolidate the powders into a dense metal pellet. XRD analysis of the final product showed that the metal oxide pellets were successfully reduced.
The oxygen content of the alloy was approximately 0.1-0.2 wt %, analysed by inert gas fusion. Approximately 0.5 g of the metal alloy was obtained per pellet.
Whilst the foregoing description has described exemplary embodiments, it will be understood by those skilled in the technology concerned that many variations may be made without departing from the present invention.
| Number | Date | Country | Kind |
|---|---|---|---|
| 10201902252U | Mar 2019 | SG | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/SG2020/050132 | 3/12/2020 | WO | 00 |
