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
  • C25B11/00—Electrodes; Manufacture thereof not otherwise provided for
  • C25B11/04—Electrodes; Manufacture thereof not otherwise provided for characterised by the material
  • C25B11/051—Electrodes formed of electrocatalysts on a substrate or carrier
  • C25B11/073—Electrodes formed of electrocatalysts on a substrate or carrier characterised by the electrocatalyst material
  • C25B11/075—Electrodes formed of electrocatalysts on a substrate or carrier characterised by the electrocatalyst material consisting of a single catalytic element or catalytic compound
  • C25B11/077—Electrodes formed of electrocatalysts on a substrate or carrier characterised by the electrocatalyst material consisting of a single catalytic element or catalytic compound the compound being a non-noble metal oxide
• • 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
• • 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
  • C25B11/00—Electrodes; Manufacture thereof not otherwise provided for
  • C25B11/04—Electrodes; Manufacture thereof not otherwise provided for characterised by the material
  • C25B11/051—Electrodes formed of electrocatalysts on a substrate or carrier
  • C25B11/073—Electrodes formed of electrocatalysts on a substrate or carrier characterised by the electrocatalyst material
  • C25B11/091—Electrodes formed of electrocatalysts on a substrate or carrier characterised by the electrocatalyst material consisting of at least one catalytic element and at least one catalytic compound; consisting of two or more catalytic elements or catalytic compounds

Definitions

• the present invention relates to a method of stabilising the activity of electrodes coated with mixed oxide electrocatalysts during use in electrochemical cells.
• An electrochemical cell is a device which has as basic components at least one anode and one cathode and an electrolyte.
• the cell may use electrical energy to carry out a chemical reaction such as the oxidation or reduction of a chemical compound as in an electrolytic cell. Alternatively, it can convert inherent chemical energy in a conventional fuel into low voltage direct current electrical energy as in a fuel cell..
• the electrodes, particularly the cathode, in such a cell may be of relatively inexpensive material such as massive iron. However, electrodes of such material tend to result in very low activity. These problems may be overcome to a degree by using electrodes activated with precious metals such as platinum. In such cases these precious metals are used as catalytic coatings on the surface of an electrode core of inexpensive material. Such catalyst coatings are termed electro- catalysts. However, the use of precious metals in this manner results in high cost electrodes.
• electrochemical cells having a hydrogen electrode Such electrochemical cells are used for several purposes, for example, the electrolysis of water to produce hydrogen and oxygen, in chlorine cells in which brine is electrolysed and in fuel cells which generate power by the oxidation of fuel. Of these processes, the electrolysis of water is used on an industrial scale for producing high purity hydrogen.
• the voltage, V, applied across the electrodes can be divided into three components, the decomposition voltage of water, E d , the overvoltage at the electrodes, E o , and the Ohmic loss in the inter-electrode gap which is the product of the cell current, I, and the electrical resistance (including the membrane resistance) of this gap, R.
• Activation overvoltage results from the slowness of the reactions at the electrode surface and varies with the metal of the electrode and its surface condition. It may be reduced by operating at elevated temperatures and/or by using improved electrocatalysts but increases with the current density of the electrode reaction.
• cathodes containing precious metal electrocatalysts such as platinum, for example, does achieve a reduction in activation overvoltage.
• the technical advantage to be obtained by the use of such precious metal electro ⁇ catalysts is substantially offset by the expense.
• the use of mixed cobalt/molybdenum oxide as electrocatalyst has also been suggested. Such an electrode, made by painting a nickel gauze with a mixed cobalt/molybdenum oxide electrocatalyst and polytetrafluorethylene
• the present invention is an electrochemical cell with an electrode having deposited thereon an electrocatalyst which is a mixed oxide of nickel-molybdenum, nickel-tungsten, cobalt- molybdenum or cobalt-tungsten and containing an aqueous alkaline electrolyte comprising an aqueous solution of a molybdenum, vanadium or tungsten compound.
• the aqueous alkaline solution in the electrolyte suitably contains an alkali metal hydroxide in solution, preferably sodium hydroxide or potassium hydroxide.
• an alkali metal hydroxide in solution preferably sodium hydroxide or potassium hydroxide.
• aqueous solutions of potassium hydroxide are preferred due to their having greater conductivity than that of other hydroxides.
• the molybdenum, vanadium or tungsten compound is suitably added to the electrolyte as an oxide.
• the chemical composition of the oxides of molybdenum, vanadium or tungsten in solution is uncertain and it is assumed that they exist as molybdate, vanadate or tungstate ions respectively.
• the molybdate, vanadate or tungstate ion may be introduced into the electrolyte solution by dissolving a compound of molybdenum, vanadium or tungsten, for example, molybdenum trioxide, vanadium pentoxide, tungsten trioxide, sodium molybdate, sodium vanadate, sodium tungstate, potassium molybdate, potassium vanadate, potassium tungstate or ammonium molybdate, ammonium vanadate or a ⁇ monium tungstate in aqueous solution.
• a compound of molybdenum, vanadium or tungsten for example, molybdenum trioxide, vanadium pentoxide, tungsten trioxide, sodium molybdate, sodium vanadate, sodium tungstate, potassium molybdate, potassium vanadate, potassium tungstate or ammonium molybdate, ammonium vanadate or a ⁇ monium tungstate in aqueous solution.
• the concentration of the molybdenum, vanadium or tungsten compound in the electrolyte solution is suitably in the range of 0.005 and 5 grams per 100 ml of the electrolyte most preferably between 0.1 and 1 gram per 100 ml calculated.as the trioxide for molybdenum and tungsten and as the pentoxide for vanadium.
• concentration of the molybdenum, vanadium or tungsten compound in the electrolyte solution is suitably in the range of 0.005 and 5 grams per 100 ml of the electrolyte most preferably between 0.1 and 1 gram per 100 ml calculated.as the trioxide for molybdenum and tungsten and as the pentoxide for vanadium.
• One of the principal advantages of using an electrolyte containing a compound of molybdenum, vanadium or tungsten is that it stabilises electrodes coated with mixed oxide electrocatalysts.
• the electrodes coated with the mixed oxide electrocatalysts and used in the present invention are preferably prepared by alternately coating an electrode core with a compound of nickel or cobalt, and with a compound of molybdenum or tungsten, said compounds being capable of thermal decomposition to the corresponding oxides, heating the coated core at an elevated temperature to form a layer of the mixed oxides on the core and finally curing the core with the mixed oxide layer thereon in a reducing atmosphere at a temperature between 350°C and 600°C.
• the core material on which the coating is carried out may be of a relatively inexpensive material such as nickel or massive iron.
• the material may be in the form of wire, tube, rod, planar or curved sheet, screen or gauze. A nickel screen is preferred.
• the compound of nickel or cobalt is suitably a nitrate and the compound of molybdenum or tungsten is suitably a molybdate or tungstate, preferably ammonium paramolybdate or ammonium tungstate.
• the coating may be applied onto the core by dipping the core in a solution of the compound or by spraying a solution of the compound on the core.
• the dipping may be carried out in the respective solutions of the compounds in any order and is preferably carried out several times.
• the coated core is heated to decompose the compounds into the corresponding oxides.
• the heating is suitably carried out at a temperature between 400 and 1200°C, preferably between
• the electrode core covered with a layer of the mixed oxides in this manner is then cured in an oven in a reducing atmosphere at a temperature between 350°C and 600°C, preferably between 450°C and 600°C.
• the reducing atmosphere is preferably pure hydrogen and the reduction is suitably carried out at atmospheric pressure.
• the electrode core suitably has an electrocatalyst loading of at least 10 mg/cm 2 , preferably between 10 and 100 mg/cm 2 and most preferably between 40 and 100 mg/cm 2 .
• the loading is the difference between the weight of the electrode core before deposition of the oxides and the weight thereof after deposition followed by curing in a reducing atmosphere.
• the mixed oxide electrocatalysts used in the present invention may contain in addition to the two metal oxides a minor proportion of an alloy of the oxide forming metals which may be due to the reduction of the oxides during the curing step.
• Electrodes coated with such electrocatalysts can be installed as cathodes or anodes in electrochemical cells according to the present invention without substantial loss of activity of the electrode if left immersed on an open circuit during inoperative periods.
• the stabilisation of activity thus achieved enables cheaper electrocatalysts to be used instead of the more expensive platinum type electrocatalysts especially in commercial water electrolysers and chlorine cells, and thereby significantly improves the economic efficiency of these cells.
• the invention is further illustrated with reference to the following Examples. All electrochemical measurements in the following Examples were carried out as follows unless otherwise stated.
• the activity of prepared electrodes was determined by mea ⁇ uri ⁇ g f - their potential against reference electrodes when a constant current was passed as indicated below. A three compartment cell was used for the measurements. Nickel screens were used as anodes and either a Dynamic Hydrogen Electrode (DHE) or a Saturated Calomel Electrode (SCE) were used as the reference electrode.
• DHE Dynamic Hydrogen Electrode
• SCE Saturated Calomel Electrode
• the electrolyte was 30% w/v potassium hydroxide (approx 5N); all experiments were conducted at 70°C unless otherwise stated.
• Electrode potentials were IR. corrected using the interrupter technique and are quoted with respect to the DHE. Electrode potentials are reproducible to ⁇ 10 mV. The potential of the DHE with respect to the normal hydrogen electrode under the conditions specified above is -60 mV. Example 1
• a clean weighed nickel screen (1 cm x 1 cm) was dipped alterna ⁇ tively intseparate solutions of 2 molar nickel nitrate and a 0.08 molar ammonium paramolybdate. After every dipping the screen was heated in a blue bunsen flame to red heat (700-900°C). The operation was repeated several times until the screen was completely covered by a layer of mixed oxides. The electrode was then heated in an oven under an atmosphere of hydrogen at a range of temperatures. Finally the activity of the electrodes was measured as described above.
• Electrodes cured under an atmosphere of hydrogen in an oven at various temperatures were prepared as in (i) above and. tested as cathodes using an alkaline electrolyte. Table 2 summarises the results obtained. Results in Table 2 show that the best temperature ranges for the hydrogen treatment is 350-600°C.
• Electrodes were prepared from a 3.4 molar solution of nickel nitrate and a 0.143 molar solution of ammonium molybdate as described in Example 2 above. The electrodes were heated at 400°C under hydrogen for one hour. The electrode activities were determined in two solutions:
• Solution A a solution containing 12% w/v sodium hydroxide and 15% w/v sodium chloride.
• Solution B a solution containing 12% w/v sodium hydroxide

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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)
• Electrodes For Compound Or Non-Metal Manufacture (AREA)
• Electrolytic Production Of Non-Metals, Compounds, Apparatuses Therefor (AREA)
• Battery Electrode And Active Subsutance (AREA)
• Fuel Cell (AREA)
• Inert Electrodes (AREA)

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• 1979
  • 1979-02-27 CA CA000322349A patent/CA1117589A/en not_active Expired
  • 1979-03-01 IN IN147/DEL/79A patent/IN151338B/en unknown
  • 1979-03-01 IT IT20677/79A patent/IT1113031B/it active
  • 1979-03-02 EP EP79300322A patent/EP0004169B1/en not_active Expired
  • 1979-03-02 DE DE7979300322T patent/DE2961934D1/de not_active Expired
  • 1979-03-02 ES ES478256A patent/ES478256A1/es not_active Expired
  • 1979-03-05 JP JP50044879A patent/JPS55500219A/ja active Pending
  • 1979-03-05 WO PCT/GB1979/000040 patent/WO1979000709A1/en not_active Ceased
  • 1979-03-05 US US05/170,668 patent/US4426269A/en not_active Expired - Lifetime
  • 1979-11-01 DK DK463179A patent/DK463179A/da unknown

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