IP Library Granted Patent US 11,634,827
Granted Patent B2
US 11,634,827 · App. 13/877,942 · Granted Apr 25, 2023

Anode for electrolytic evolution of chlorine

Inventors: Christian Urgeghe (Redecesio-Segrate, IT); Chiara Pezzoni (Cassina de' Pecchi, IT); Antonio Lorenzo Antozzi (Merate, IT)
Assignee: INDUSTRIE DE NORA S.P.A.
C25B11/093
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Quick Facts
Patent No.
US 11,634,827
App. No.
13/877,942
Granted
Apr 25, 2023
Kind
B2
Abstract

An electrode suitable for chlorine evolution in electrolysis cells consists of a metal substrate coated with two distinct compositions applied in alternate layers, the former comprising oxides of iridium, ruthenium and valve metals, for instance tantalum, and the latter comprising oxides of iridium, ruthenium and tin. The thus-obtained electrode couples excellent characteristics of anodic potential and selectivity towards the chlorine evolution reaction.

Claims (33)

1. An electrode for evolution of gaseous products in electrolytic cells consisting of a metal substrate coated with a plurality of alternating layers of at least one first catalytic composition and at least a second catalytic composition,

said first catalytic composition comprises a mixture of oxides of iridium, of ruthenium and of at least one valve metal and being free of tin,

said second catalytic composition comprises a mixture of oxides of iridium, of ruthenium, of tin, niobium and at least one noble metal selected from the group consisting of palladium and platinum,

wherein the innermost of said plurality of alternating layers corresponds to said first catalytic composition,

wherein the electrode reduces chlorine overvoltage without reduction in oxygen overvoltage,

wherein said valve metal of said first catalytic composition is titanium and said oxides of iridium, ruthenium and titanium present in said first catalytic composition are Ru=10-30%, Ir=5-25%, Ti=35-80% atomic percentage referred to the metals, and

wherein said second catalytic layer is obtained by applying a solution containing precursors of ruthenium, iridium, tin, niobium, and at least one noble metal selection from the group consisting of palladium and platinum, wherein tin is in the form of tin hydroxyacetochloride such that after thermal treatment said oxides of iridium, of ruthenium and of tin present in said second catalytic composition are Ru=20-60%, Ir=1-20%, Sn=35-65%, atomic percentage referred to the metals, wherein Nb and at least Pd or Pt make up the remainder of the composition's atomic proportions.

2. The electrode according to claim 1 wherein in said first catalytic composition platinum is present in a 0.1-5% atomic percentage referred to the metals.

3. The electrode according to claim 1 wherein in said second catalytic composition platinum or palladium is present in an overall 0.1-10% atomic percentage referred to the metals.

4. The electrode according to claim 1 wherein in said second catalytic composition niobium is present in a 0.1-3% atomic percentage referred to the metals.

5. The electrode according to claim 1 wherein the first catalytic composition comprises oxides of Ru, Ir and Ti and are present in said first catalytic composition in a Ru=16-30%, Ir=9-20%, Ti=50-73% atomic percentage referred to the metals.

6. The electrode according to claim 1 wherein in said second catalytic composition oxides of Ru, Ir, Sn, Nb, and Pd or Pt are present in a Ru=20-30%, Ir=1-10%, Sn=59-65%, and Pd=10% or Pt=5% atomic percentage referred to the metals.

7. An electrolysis cell of alkali chloride solutions comprising the electrode of claim 1 as chlorine-evolving anode.

8. An electrode for evolution of gaseous products in electrolytic cells consisting of a metal substrate coated with a plurality of alternating layers of at least one first catalytic composition and at least a second catalytic composition,

said first catalytic composition comprises a mixture of oxides of iridium, of ruthenium, of platinum and of at least one valve metal and being free of tin,

said second catalytic composition comprises a mixture of oxides of iridium, of ruthenium, of tin, niobium and at least one noble metal selected from the group consisting of palladium and platinum,

wherein the innermost of said plurality of alternating layers corresponds to said first catalytic composition,

wherein the electrode reduces chlorine overvoltage without reduction in oxygen overvoltage,

wherein said valve metal of said first catalytic composition is titanium and said oxides of iridium, ruthenium, platinum, and titanium present in said first catalytic composition are Ru=10-30%, Ir=5-25%, Ti=35-80% atomic percentage referred to the metals, wherein Pt makes up the remainder of the composition's atomic proportions. and

wherein said second catalytic layer is obtained by applying a solution containing precursors of ruthenium, iridium, tin, niobium, and at least one noble metal selection from the group consisting of palladium and platinum, wherein tin is in the form of tin hydroxyacetochloride such that after thermal treatment said oxides of iridium, of ruthenium and of tin present in said second catalytic composition are Ru=20-60%, Ir=1-20%, Sn=35-65%, atomic percentage referred to the metals, wherein Nb and at least Pd or Pt make up the remainder of the composition's atomic proportions.

9. The electrode according to claim 8 wherein in said first catalytic composition platinum is present in a 0.1-5% atomic percentage referred to the metals.

10. The electrode according to claim 8 wherein in said second catalytic composition platinum or palladium is present in an overall 0.1-10% atomic percentage referred to the metals.

11. The electrode according to claim 8 wherein in said second catalytic composition niobium is present in a 0.1-3% atomic percentage referred to the metals.

12. A method for manufacturing the electrode according to claim 1 comprising the execution of the following sequential steps on a metal substrate:

a. applying a first solution containing the precursors of the components of said first catalytic composition;

b. optionally drying at 50-200° C. for a time of 5 to 60 minutes;

c. decomposing said first solution by thermal treatment at 400-850° C. for a time not lower than 3 minutes in the presence of air;

d. applying a second solution containing the precursors of the components of said second catalytic composition;

e. optionally drying at 50-200° C. for a time of 5 to 60 minutes;

f. decomposing said second solution by thermal treatment at 400-850° C. for a time not lower than 3 minutes in the presence of air; and

g. optionally repeating steps a-c or the whole sequence of steps a-f once or more times.

13. The method according to claim 12 wherein the sequence consisting of steps a-c and the sequence consisting of steps d-f are reversed.

14. The method according to claim 12 wherein the sequence consisting of steps a-c is repeated more than once before step d, and the sequence of steps d-f is repeated more than once before step g.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 5, 2013
From: URGEGHE, CHRISTIAN; PEZZONI, CHIARA; ANTOZZI, ANTONIO LORENZO
To: INDUSTRIE DE NORA S.P.A.
Reel/Frame 030158/0058 →
Priority Claims (1)
IT MI2010A002193 · Nov 26, 2010 · national
Continuity (1)
Related Publication 20130186750A1 · Jul 25, 2013
Cited By (2)
US 12,448,693 US 12,624,469