EP1049815B1

EP1049815B1 - Method for producing surface coated non-carbon metal-based anodes for aluminium production cells

Info

Publication number: EP1049815B1
Application number: EP99900107A
Authority: EP
Inventors: Vittorio De Nora
Original assignee: Moltech Invent SA
Current assignee: Moltech Invent SA
Priority date: 1998-01-20
Filing date: 1999-01-19
Publication date: 2003-04-09
Anticipated expiration: 2019-01-19
Also published as: EP1049815A1; DE69906697D1; NO20003704D0; AU747906B2; AU1779599A; NO20003704L; CA2317595A1; WO1999036591A1; DE69906697T2

Description

This invention relates to a method for producing non-carbon, metal-based anodes provided with an electrochemical active surface coating for use in cells for the electrowinning of aluminium by the electrolysis of alumina dissolved in a molten fluoride-containing electrolyte.

The technology for the production of aluminium by the electrolysis of alumina, dissolved in molten cryolite, at temperatures around 950°C is more than one hundred years old.

This process, conceived almost simultaneously by Hall and Héroult, has not evolved as many other electrochemical processes.

The anodes are still made of carbonaceous material and must be replaced every few weeks. The operating temperature is still not less than 950°C in order to have a sufficiently high solubility and rate of dissolution of alumina and high electrical conductivity of the bath.

The carbon anodes have a very short life because during electrolysis the oxygen which should evolve on the anode surface combines with the carbon to form polluting CO₂ and small amounts of CO and fluorine-containing dangerous gases. The actual consumption of the anode is as much as 450 Kg/Ton of aluminium produced which is more than 1/3 higher than the theoretical amount of 333 Kg/Ton.

Several improvements were made in order to increase the lifetime of the anodes of aluminium electrowinning cells, usually by improving their resistance to chemical attacks by the cell environment and air to those parts of the anodes which remain outside the bath. However, most attempts to increase the chemical resistance of anodes were coupled with a degradation of their electrical conductivity.

US Patent 4,614,569 (Duruz/Derivaz/Debely/Adorian) describes metal-based anodes for aluminium electrowinning coated with a protective coating of cerium oxyfluoride, formed in-situ in the cell or pre-applied, this coating being maintained by the addition of cerium compounds to the molten cryolite electrolyte. This made it possible to have a protection of the surface only from the electrolyte attack and to a certain extent from the gaseous oxygen but not from the nascent monoatomic oxygen.

EP Patent application 0 306 100 (Nyguen/Lazouni/Doan) describes anodes composed of a chromium, nickel, cobalt and/or iron based substrate covered with an oxygen barrier layer and a ceramic coating of nickel, copper and/or manganese oxide which may be further covered with an in-situ formed protective cerium oxyfluoride layer.

Likewise, US Patents 5,069,771, 4,960,494 and 4,956,068 (all Nyguen/Lazouni/Doan) disclose aluminium production anodes with an oxidised copper-nickel surface on an alloy substrate with a protective barrier layer. However, full protection of the alloy substrate was difficult to achieve.

A significant improvement described in US Patent 5,510,008, and in International Application WO96/12833 (Sekhar/Liu/Duruz) involved a micropyretically produced body of nickel, aluminium, iron and copper whose surface is oxidised before use or in-situ. By said micropyretic methods materials have been obtained whose surfaces, when oxidised, are active for the anodic reaction and whose metallic interior has low electrical resistivity to carry a current from high electrical resistant surface to the busbars. However it would be useful, if it were possible, to simplify the manufacturing process of these materials and increase their life to make their use economic.

Metal or metal-based anodes are highly desirable in aluminium electrowinning cells instead of carbon-based anodes. Many attempts were made to use metallic anodes for aluminium production, however they were never adopted by the aluminium industry because of their poor performance.

An object of the invention is to reduce substantially the consumption of an applied electrochemically active anode surface coating of a metal-based non-carbon anode for aluminium electrowinning cells which coating is in contact with the electrolyte.

Another object of the invention is to provide a surface coating for a metal-based anode for aluminium electrowinning cells which in addition to a long life has a high electrochemical activity and can easily be applied onto an anode substrate.

A major object of the invention is to provide an anode for the electrowinning of aluminium which has no carbon so as to eliminate carbon-generated pollution and reduce the high cell operating costs.

The invention relates to a method of applying a coating which is made of oxides that comprise ferrites and/or chromites and which is electrically conductive and electrochemically active for the oxidation of oxygen ions, onto an oxidation-resistant metal-based anode substrate to produce a non-carbon, metal-based, high temperature resistant aluminium production anode for the electrolysis of alumina dissolved in a fluoride-containing electrolyte. The coating comprises: at least one ferrite selected from cobalt, manganese, nickel, magnesium and zinc ferrite; and/or at least one chromite selected from iron, cobalt, copper, manganese, beryllium, calcium, strontium, barium, magnesium, nickel and zinc chromite.

According to the invention, the method comprises applying onto the anode substrate a plurality of applied layers of the electrically conductive and electrochemically active coating, the layers being selected from: layers of liquid solutions; layers of liquid dispersions and pasty dispersions; layers of liquid suspensions and pasty suspensions; and layers of pasty slurries and non-pasty slurries, and combinations thereof, with or without heat treatment between two consecutively applied layers. At least one of these layers contains a polymeric and/or colloidal carrier. The method of the invention further comprises exposing the applied layers to a final heat treatment so as to form the electrically conductive and the electrochemically active oxide coating that comprises the ferrite(s) and/or chromite(s) from the applied layers.

At least one applied layer of the coating comprises: one or more dried colloids selected from colloidal alumina, silica, yttria, ceria, thoria, zirconia, tin oxide and nickel-ferrite; and/or one or more dried inorganic polymers selected from polymeric nickel aluminate, magnesium chromite and magnesium ferrite.

During use of the anode, the oxidation of oxygen ions forms monoatomic nascent oxygen which may as such or as biatomic molecular gaseous oxygen oxidise or further oxidise the surface of the multi-layer coating, or part or most of the multi-layer coating or the surface of the substrate, to form a limited barrier to ionic and nascent monoatomic oxygen and at least a limited barrier to gaseous oxygen.

The multi-layer coating may have a slow dissolution rate in the fluoride-containing electrolyte.

In the context of this invention:

a metal-based anode means that the anode contains mainly one or more metals in the anode substrate as such or as alloys, intermetallics and/or cermets.
a liquid solution means a liquid containing ionic species which are smaller than 5 nanometers and/or polymeric species of 5 to 10 nanometers and no larger particles;
a dispersion means a liquid containing particles in colloidal form, wherein the size of the largest particles is comprised between 10 and 100 nanometers;
a suspension means a liquid containing particles in which the largest particles are comprised between 100 and 1000 nanometers; and
a slurry means a liquid containing particles the size of which exceeds 1000 nanometers.

Advantageously, the metal-based substrate comprises at least one metal selected from nickel, copper, cobalt, chromium, molybdenum, tantalum and iron, and mixtures thereof, as metals and/or oxides, in one or more layers.

Preferably, the metal-based substrate comprises a surface pre-coating or pre-impregnation. The pre-coating or pre-impregnation may for instance comprise ceria.

The multi-layer coating may comprise one or more oxides and/or oxyfluorides, and combinations thereof, such as spinels and/or perovskites. For instance, the electrochemically active layer may contain doped, non-stoichiometric and/or partially substituted spinels, the doped spinels comprising dopants selected from the group consisting Ti⁴⁺, Zr⁴⁺, Sn⁴⁺, Fe⁴⁺, Hf⁴⁺, Mn⁴⁺, Fe³⁺, Ni³⁺, Co³⁺, Mn³⁺, Al³⁺, Cr³⁺, Fe²⁺, Ni²⁺, Co²⁺, Mg²⁺, Mn²⁺, Cu²⁺, Zn²⁺ and Li⁺.

The oxide may be present in the electrochemically active multi-layer coating as such, or in a multi-compound mixed oxide and/or in a solid solution of oxides. The oxide may be in the form of a simple, double and/or multiple oxide, and/or in the form of a stoichiometric or non-stoichiometric oxide.

The multi-layer coating may comprise a ferrite, such as a ferrite selected from cobalt, manganese, nickel, magnesium and zinc ferrite, and mixtures thereof. The ferrite may be doped with at least one oxide selected from chromium, titanium, tin and zirconium oxide. Nickel ferrite may be partially substituted with divalent iron (Fe²⁺).

Alternatively, the multi-layer coating may comprise a chromite, such as a chromite selected from iron, cobalt, copper, manganese, beryllium, calcium, strontium, barium, magnesium, nickel and zinc chromite.

Advantageously, the multi-layer coating may comprise an electrocatalyst for the formation of molecular oxygen from atomic oxygen, selected from iridium, palladium, platinum, rhodium, ruthenium, silicon, tin and zinc, the Lanthanide series and Mischmetal, and their oxides, mixtures and compounds thereof.

At least one layer of the multi-layer coating may also comprise one or more dried colloids or polymers, for example selected from the group consisting of colloidal alumina, silica, yttria, ceria, thoria, zirconia, magnesia, lithia, tin oxide, zinc oxide, monoaluminium phosphate or cerium acetate. The colloid or polymer may be derived from colloid or polymer precursors and reagents which are solutions of at least one salt such as chlorides, sulfates, nitrates, chlorates, perchlorates or metal organic compounds such as alkoxides, formates, acetates of aluminium, silicon, yttrium, cerium, thorium zirconium, magnesium and lithium. Possibly, the solutions of metal organic compounds, principally metal alkoxides, are of the general formula M(OR)_z where M is a metal or complex cation, R is an alkyl chain and z is a number, preferably from 1 to 12. The colloid or polymer precursor or reagent may also contain a chelating agent such as acetyl acetone or ethylacetoacetate.

In one embodiment at least one layer below the electrochemically active surface, which may be a solid or liquid applied layer, constitutes a barrier to oxygen, such as a chromium or black non-stoichiometric nickel layer. The oxygen barrier layer may in turn be covered with a protective barrier preventing its dissolution, such as a nickel and/or copper layer.

Several techniques may be used to apply the layers such as painting, spraying, dipping, brush, electroplating or rollers.

Each liquid-applied layer may be allowed to dry at least partially in the ambient air or assisted by heating before applying the next layer.

The multi-layer coating may be also formed by applying onto the metal-based substrate a precursor containing constituents which react among themselves to form the coating, and reacting the constituents to form the multi-layer coating. Alternatively, the multi-layer coating may be formed by applying onto the metal-based substrate a precursor containing at least one constituent which reacts with the metal-substrate to form the multi-layer coating, and reacting the constituent(s) with the metal-substrate to form the coating.

A solid-applied layer may be applied onto the metal-substrate by plasma spraying, arc spraying, physical vapour deposition, chemical vapour deposition or calendering rollers.

The above methods may also be applied for reconditioning an anode as described above whose electrochemically active multi-layer coating is worn or damaged. The method comprises clearing at least worn out and/or damaged parts of the active coating from the substrate and then reconstituting at least the electrochemically active coating.

A further object of the invention is a method of producing aluminium in a cell, comprising manufacturing an anode by applying an electrically conductive and electrochemically active oxide coating onto an oxidation-resistant metal-based anode substrate as described above, introducing the anode into the cell, dissolving alumina in a fluoride-containing electrolyte, such as cryolite, of the cell and electrolysing the dissolved alumina to produce aluminium.

Preferably, the cell comprises an aluminium-wettable cathode. Even more preferably, the cell is in a drained configuration by having at least one drained cathode on which aluminium is produced and from which aluminium continuously drains.

The cell may be of monopolar, multi-monopolar or bipolar configuration. A bipolar cell may comprise the anodes as described above as a terminal anode or as the anode part of a bipolar electrode.

Advantageously, the cell may comprise means to circulate the electrolyte between the anodes and facing cathodes and/or means to facilitate dissolution of alumina in the electrolyte.

The cell may be operated with the electrolyte at conventional temperatures, such as 950 to 970°C, or at reduced temperatures as low as 750°C.

The invention will be further described in the following Examples:

Example 1

A polymeric slurry was prepared from: a non-dispersable but suspendable particulate consisting of a nickel-ferrite powder and a nickel aluminate (NiOAl₂O₃) precursor material acting as a polymeric carrier and binder for the nickel ferrite powder. The nickel-ferrite powder was specially prepared; however, commercially-available products could also have been used. The precursor NiOAl₂O₃ materials, solution and gel powder reacted to form the spinel NiAl₂O₄ at < 1000°C.

When applied to a suitably prepared substrate such as nickel, this slurry produced an oxide coating made from the pre-formed or the in-situ formed nickel ferrite which adhered well onto the substrate and formed a coherent coating when dried and heated. The slurry could be applied by a simple technique such as brushing or dipping to give a coating of pre-determined thickness.

An anode was made by brushing 15 layers of this slurry onto a substrate in order to obtain a final coating of a thickness of about 150 micron. The substrate consisted of 74 weight% nickel, 17 weight% chromium and 9 weight% iron, such as Inconel®. Each applied layer was allowed to dry for 10 minutes at 100°C before applying a further layer. The slurry-brushed substrate was then submitted to a final heat treatment at 450-500°C 15 minutes. X-ray diffraction showed nickel-aluminate had formed in the coating.

The anode was then tested in an electrolytic cell containing cryolite at 960°C wherein alumina was dissolved in a amount of 6 weight%. After 15 hours the anode was extracted and showed no signs of substantial corrosion.

Example 2

A carrier consisting of a nickel aluminate polymeric solution containing a non-dispersed but suspended particulate of nickel aluminate was made by heating 75 g of Al(NO₃)₃.9 H₂O (0.2 moles Al) at 80°C to give a concentrated solution which readily dissolved 12 g of NiCO₃ (0.1 moles). The viscous solution (50 ml) contained 200 g/l Al₂O₃ and 160 g/l NiO (total oxide, >350 g/l).

This nickel-rich polymeric concentrated anion deficient solution was compatible with commercially-available alumina sols e.g. NYACOL™.

A stoichiometrically accurate NiO.Al₂O₃ mixture was prepared by adding 5 ml of the anion deficient solution to 2.0 ml of a 150 g/l alumina sol; this mixture was stable to gelling and could be applied to smooth metal and ceramic surfaces by a dip-coating technique. When heated to 450-500°C, X-ray diffraction showed nickel-aluminate had formed in the coating.

Other non-dispersable particulate than nickel aluminate could be suspended in the anion-deficient nickel aluminate precursor solution and applied as coatings which when heat-treated would form nickel-aluminate containing the added oxides.

An anode was then prepared and tested as described in Example 1 and showed similar results.

Example 3

A colloidal solution containing a metal ferrite precursor (as required for NiONiFe₂O₄) was prepared by mixing 20.7 g Ni(NO₃)₂.6 H₂O (5.17 g NiO) with 18.4 g Fe(NO₃)₃.9 H₂O (4.8 g Fe₂O₃) and dissolving the salts in water to a volume of 30 ml. The solution was stable to viscosity changes and to precipitation when aged for several days at 20°C.

An organic solvent such as PRIMENE™ JMT (R₃CNH₂ molecular weight ∼350) is immiscible with water and extracts nitric acid from acid and metal nitrate salt solutions. An amount of 75 ml of the PRIMENE™ JMT (2.3 M) diluted with an inert hydrocarbon solvent was mixed with 10 ml of the colloidal nickel-ferrite precursor solution. Within a few minutes the spherical droplets of feed were converted to a mixed oxide gel; they were filtered off, washed with acetone and dried to a free-flowing powder. When the gel was heated in air, nickel-ferrite formed at < 800°C and the powder could be used as a non-dispersable but suspended particulate in colloidal and/or inorganic polymeric slurries as described in Example 1 or 2. Commercially-available nickel-ferrite powder could also have been used.

As described in Example 1, an anode was then prepared by coating a nickel plated copper core covered with a chromium based oxygen barrier layer and a nickel-copper protective barrier layer preventing dissolution of the chromium layer with this slurry, tested and showed similar results.

Example 4

An amount of 5 g of NiCO₃ was dissolved in a solution containing 35 g Fe(NO₃)₃.9 H₂O to give a mixture (40 ml) having the composition required for the formation of NiFe2O₄. The solution was converted to colloidal gel particles by solvent extracting the nitrate with PRIMENE™ JMT as described in Example 3. The nickel-ferrite precursor gel was calcined in air to give a non-dispersable but suspended particulate in the form of a nickel-ferrite powder, which could be hosted into nickel-aluminate carrier for coating applications from colloidal and/or polymeric slurries.

A 200 micron thick coating consisting of 15 superimposed layers was obtained on an Inconel® substrate as in Example 1 by dipping the substrate in this slurry. As in Example 1, each layer was allowed to dry before applying a further layer.

The coated substrate was then submitted to a final heat treatment at 600°C for 1 hour to consolidate the coating and form an anode.

The anode was then tested in a cell as in Example 1 and showed similar results.

Example 5

An amount of 100 g of Cr(NO₃)₃.9 H₂O was heated to dissolve the salt in its own water of crystallisation to form a solution containing 19 g Cr₂O₃. The solution was heated to 120°C and 12.5 g of magnesium-hydroxy carbonate containing the equivalent of 5.0 g MgO was added. Upon stirring a solution was obtained in the form of an anion-deficient polymer mixture with a density of approximately 1.5 g/cm³ suitable to act as a carrier. An amount of 50 g of this carrier was evaporated to dryness to convert the solution into a fine oxide powder. The oxides were then calcined at 600°C into a magnesium chromite powder to form a non-dispersable but suspended particulate.

After grinding to a fine powder, the magnesium chromite particulate was suspended in the polymer carrier to form a slurry suitable for coating treated metal substrates.

An anode was then prepared and tested as in Example 4 and showed similar results.

Example 6

An amount of 150 g of Fe(NO₃)₃.9 H₂O was heated to dissolve the salt in its own water of crystallisation to form a solution containing 29 g Fe₂O₃. The solution was heated to 120°C and 18.9 g of magnesium hydroxy-carbonate dissolved in the hot solution to form 7.5 g MgO in form of an inorganic polymer together with Fe₂O₃. An amount of 50 g of the polymer solution was evaporated to dryness and then calcined at 600°C yielding approximately 13 g of magnesium ferrite powder.

After calcination, the ferrite powder was ground in a pestle and mortar and then dispersed in the same inorganic polymer to give a slurry that was used to coat a treated metal substrate.

An anode was then prepared and tested as in Example 3 and showed similar results.

Example 7

A cleaned surface of an Inconel™ billet (typically comprising 76 weight% nickel - 15.5 weight% chromium - 8 weight% iron) was pre-coated with a ceria colloid as described in US Patent 4,356,106 (Woodhead/Raw), dried and heated in air at 500°C. The pre-coated billet was then further coated with the polymeric slurry described in Example 1 or 2, dried and heated in air at 500°C. The ferrite coating was very adherent and successive layers of the slurry could be applied to build up a coating of ferrite/aluminate having a thickness above 100 micron.

A similar untreated Inconel™ billet was coated with a 10 micron thick layer using the polymeric slurry described in Example 1 or 2 but without pre-coating the billet with ceria colloid. After heat-treatment the coating was cracked and easily broke away from the substrate, which demonstrated the effect of the ceria pre-coat.

An anode was then prepared and tested as in Example 1 and showed similar results.

Example 8

A test anode was made by coating by electrodeposition a core structure in the shape of a rod having a diameter of 12 mm consisting of 74 weight% nickel, 17 weight% chromium and 9 weight% iron, such as Inconel®, first with a nickel layer about 200 micron thick and then a copper layer about 100 micron thick.

The coated structure was heat treated at 1000°C in argon for 5 hours. This heat treatment provides for the interdiffusion of nickel and copper to form an intermediate layer. The structure was then heat treated for 24 hours at 1000° at air to form a chromium oxide (Cr₂O₃) barrier layer on the core structure and oxidising at least partly the interdiffused nickel-copper layer thereby forming the intermediate layer.

A nickel-ferrite powder was made by drying and calcining at 900°C the gel product obtained from an inorganic polymer precursor solution containing ferric nitrate and nickel carbonate. A thick paste was made by mixing 1 g of this nickel-ferrite powder with 0.85 g of a nickel aluminate polymer solution containing the equivalent of 0.15 g of oxide. This thick paste was then diluted with 1 ml of water and ground in a pestle and mortar to obtain a suitable viscosity to form a nickel-based paint.

An electrochemically active oxide layer was obtained on the core structure by applying the nickel-based paint onto the core structure with a brush. The painted structure was allowed to dry for 30 minutes before heat treating it at 500°C for 1 hour to decompose volatile components and to consolidate the oxide coating.

The heat treated coating layer was about 15 micron thick. Further coating layers were applied following the same procedure in order to obtain a 200 micron thick electrochemically active coating covering the core structure.

The anode was then tested in a cryolite melt containing approximately 6 weight% alumina at 970°C by passing current at a current density of about 0.8 A/cm². After 100 hours the anode was extracted from the cryolite and showed no sign of significant internal corrosion after microscopic examination of a cross-section of the anode specimen.

Claims

A method of applying a coating which is made of oxides that comprise ferrites and/or chromites and which is electrically conductive and electrochemically active for the oxidation of oxygen ions, onto an oxidation-resistant metal-based anode substrate to produce a non-carbon, metal-based, high temperature resistant aluminium production anode for the electrolysis of alumina dissolved in a fluoride-containing electrolyte, said coating comprising:

at least one ferrite selected from cobalt, manganese, nickel, magnesium and zinc ferrite; and/or

at least one chromite selected from iron, cobalt, copper, manganese, beryllium, calcium, strontium, barium, magnesium, nickel and zinc chromite,

said method comprising applying onto the anode substrate a plurality of precursor layers of said electrically conductive and electrochemically active coating, said layers being selected from:

a) layers of liquid solutions;

b) layers of liquid dispersions and pasty dispersions;

c) layers of liquid suspensions and pasty suspensions; and

d) layers of pasty slurries and non-pasty slurries,

and combinations thereof, with or without heat treatment between two consecutively applied layers, at least one of the layers containing a polymeric and/or a colloidal carrier, and exposing the applied layers to a final heat treatment so as to form the electrically conductive and electrochemically active oxide coating that comprises the ferrite(s) and/or chromite(s) from the applied layers, at least one applied layer comprising:

one or more dried colloids selected from colloidal alumina, silica, yttria, ceria, thoria, zirconia, tin oxide and nickel-ferrite; and/or

one or more dried inorganic polymers selected from polymeric nickel aluminate, magnesium chromite and magnesium ferrite.
The method of claim 1, wherein at least one layer is applied by painting, spraying, dipping, brush, electroplating or rollers.
The method of claim 1, comprising applying at least one layer as a suspension.
The method of claim 1, wherein the substrate is pre-coated or pre-impregnated by painting, spraying, dipping or infiltration with reagents and precursors, gels and/or colloids before application of the multi-layer coating, in particular with a solution containing ceria or a ceria precursor.
The method of claim 1, wherein several liquid-containing layers are applied, each layer being allowed to dry at least partially in the ambient air or assisted by heating before applying the next layer.
The method of claim 1, comprising applying onto the metal-based substrate a precursor containing constituents which react among themselves to form the multi-layer coating, or which react with the metal-substrate to form the multi-layer coating, and reacting the constituents to form the multi-layer coating.
The method of claim 1, wherein a further layer is applied as a solid onto the metal-substrate by plasma spraying, arc spraying, physical vapour deposition, chemical vapour deposition or calendering rollers.
The method of claim 1, wherein the metal-based substrate is selected from a metal, an alloy, an intermetallic compound or a cermet.
The method claim 8, wherein the metal-based substrate comprises at least one metal selected from nickel, copper, cobalt, chromium, molybdenum, tantalum and iron, and mixtures thereof, as metals and/or oxides, in one or more layers.
The method of claim 1, wherein the multi-layer* applied coating comprises an electrocatalyst for the formation of molecular oxygen from atomic oxygen, selected from iridium, palladium, platinum, rhodium, ruthenium, silicon, tin and zinc, the Lanthanide series, Mischmetal, and their oxides, mixtures and compounds thereof.
A method of producing aluminium in a cell, comprising manufacturing an anode by applying an electrically conductive and electrochemically active oxide coating onto an oxidation-resistant metal-based anode substrate by the method defined in claim 1, introducing the anode into the cell, dissolving alumina in a fluoride-containing electrolyte of the cell and electrolysing the dissolved alumina to produce aluminium.
The method of claim 11, wherein the cell comprises an aluminium-wettable cathode.
The method of claim 12, wherein the cell comprises a drained cathode on which aluminium is produced and from which aluminium continuously drains.
The method of claim 11, wherein the cell is in a bipolar configuration, the anode forming the anodic side of a bipolar electrode or a terminal anode.
The method of claim 11, comprising circulating the electrolyte between the anode and a facing cathode.
The method of claim 11, wherein during operation the electrolyte is at a temperature of 750°C to 970°C.