Catalyst coating and process for production thereof
Abstract
A process for wet-chemical production of a catalyst coating on an electrically conductive support for electrodes for chloralkali or hydrochloric acid electrolysis with electro catalytically active components based on noble metal oxides, in which the catalyst coating is produced by; producing a coating solution or dispersion comprising a precursor compound of a noble metal and/or a metal oxide of a noble metal, and a solvent or dispersant, with addition of one or more acids to the coating solution or dispersion, where the molar ratio of the total of the amounts of acid (in mol) present in the coating solution or dispersion to the sum of the amounts of the metals from the metal-containing components present in the coating solution or dispersion is at least 2:1; applying the coating solution or dispersion to the support; substantially freeing the layer applied of solvent or dispersant by drying; and subjecting the dried layer obtained to a thermal treatment to form the catalyst coating.
Claims
exact text as granted — not AI-modified1 - 18 . (canceled)
19 . A process for wet-chemical production of a catalyst coating on an electrically conductive support for electrodes for chloralkali or hydrochloric acid electrolysis with electrocatalytically active components based on at least one noble metal oxide and/or noble metal of the noble metals of transition group VIIIa of the Periodic Table of the Elements, and optionally additionally at least one valve metal oxide, wherein the catalyst coating is produced by
a) producing a coating solution or dispersion at least comprising a precursor compound of a noble metal and/or a metal oxide of a noble metal and optionally additionally a tin and/or valve metal compound, and a solvent or dispersant, with addition of one or more acids to the coating solution or dispersion, where the molar ratio of the total of the amounts of acid (in mol) present in the coating solution or dispersion to the sum of the amounts of the metals from the metal-containing components present in the coating solution or dispersion is at least 2:1, b) applying a layer of the coating solution or dispersion to the conductive support, c) substantially freeing the layer applied of solvent or dispersant by drying and d) then subjecting the dried layer obtained to a thermal treatment at a temperature of at least 300° C., and optionally in the presence of oxygen-containing gases, to form the catalyst coating.
20 . The process according to claim 19 , wherein the coating solution or dispersion according to step a) comprises one or more acids having a pK a in aqueous solution of not more than 12.
21 . The process according to claim 19 wherein the coating solution or dispersion according to step a) additionally comprises one or more precursor compounds and/or a metal and/or a metal oxide of one or more doping elements selected from the group consisting of: aluminium, antimony, lead, iron, germanium, indium, manganese, molybdenum, niobium, tantalum, titanium, tellurium, vanadium, zinc, tin and zirconium.
22 . The process according to claim 19 wherein the thermal treatment d) is performed in the presence of air or in the presence of a mixture of oxygen and a protective gas selected from the group consisting of nitrogen, helium, neon, argon, and krypton.
23 . The process according to claim 19 wherein the drying c) is performed in the presence of air or in the presence of a mixture of oxygen and a protective gas, especially at least one protective gas selected from the group consisting of nitrogen, helium, neon, argon and krypton.
24 . The process according to claim 19 wherein the precursor compound used in step a) is a chloride of ruthenium and/or iridium.
25 . The process according to claim 19 wherein-the acid used in the coating solution in a) is an organic or inorganic acid or a combination of organic and inorganic acids.
26 . The process according to claim 25 , wherein the acid used in the coating solution is a combination of organic and inorganic acid, where the molar ratio of the amount of organic acid (in mol) present in the coating solution or dispersion to the amount of inorganic acid is 20:80 to 100:0.
27 . The process according to claim 25 wherein the acid used in the coating solution in a) is hydrochloric acid and/or a C 1 to C 4 -carboxylic acid selected from the group consisting of hydrochloric acid, formic acid, acetic acid and propionic acid.
28 . The process according to claim 19 wherein the solvent or dispersant used is one or more selected from the group consisting of water and C 1 -C 6 -alcohol.
29 . The process according to claim 19 wherein the support is based on a valve metal selected from the group consisting of titanium, zirconium, tungsten, tantalum and niobium.
30 . The process according to claim 19 wherein the surface of the support before the application b) of the coating solution or dispersion to the support is mechanically pre-cleaned-and optionally subsequently etched with an acid such as hydrochloric acid or oxalic acid for further removal of oxides on the surface.
31 . The process according to claim 19 wherein the coating solution or dispersion according to step a) additionally comprises at least one precursor compound selected from the group consisting of the compounds of aluminium, antimony, lead, iron, germanium, indium, manganese, molybdenum, niobium, tantalum, titanium, tellurium, vanadium, zinc, tin, and zirconium tin, indium, manganese and antimony, optionally also functioning as a precursor compound for a doping, in which case the proportion of doping elements is up to 20 mol % based on the total content of metals in the coating solution or dispersion.
32 . The process according to claim 31 , wherein the coating solution or dispersion according to step a) comprises one or more precursor compounds selected from the group consisting of the compounds of aluminium, antimony, tantalum, niobium, tin, and indium.
33 . The process according to claim 19 wherein the additional valve metal precursor compounds used are solvent-soluble fluorides, chlorides, iodides, bromides, nitrates, phosphates, sulphates, acetates, acetylacetonates or alkoxides of the elements titanium, zirconium, tungsten, tantalum or niobium.
34 . The process according to claim 19 wherein a catalyst coating is produced with binary mixed oxides formed from titanium oxide and ruthenium oxide by using a coating solution in a) comprising titanium(IV) butoxide and ruthenium(III) chloride (RuCl 3 ) and a mixture of acetic acid and water.
35 . An electrode having a catalyst coating obtained by a process according to claim 19 .
36 . A method for using the electrode according to claim 35 for electrochemical production of chlorine from hydrogen chloride or alkali metal chloride solutions, or for generation of electrical power, in fuel cells and batteries, in redox capacitors, for electrolysis of water, for regeneration of chromium baths, or in the case of use of fluoride-containing electrolytes in hydrogen peroxide, ozone of the peroxodisulphate production.
37 . The process according to claim 31 , wherein the coating solution or dispersion according to step a) comprises one or more precursor compounds selected from the group consisting of tin(IV) chloride (SnCl 4 ), indium(III) chloride (InCl 3 ), antimony(III) chloride (SbCl 3 ) and manganese(II) chloride (MnCl 2 ).Join the waitlist — get patent alerts
Track US2017067172A1 — get alerts on status changes and closely related new filings.
We store only your email — no account needed. See our privacy policy.