Niobium-doped titanium membranes

• US 5,028,568 A
• Filed: 07/05/1989
• Issued: 07/02/1991
• Est. Priority Date: 07/05/1989
• Status: Expired due to Term

• Current Assignee: Wisconsin Alumni Research Foundation (University of Wisconsin System)
• Original Assignee: Wisconsin Alumni Research Foundation (University of Wisconsin System)
• Inventors: Anderson, Marc A., Kikkawa, Hirofumi
• Primary Examiner(s): Dixon, Jr., William R.
• Assistant Examiner(s): Gallo, Chris
• Application Number:
  US07/376,107
• Time in Patent Office: 727 Days
• Field of Search: 501/12, 501/134, 501/152, 252/520, 252/521, 252/62.3 BT, 106/287.19, 204/290 F, 204/290 R, 204/295, 204/282, 427/126.2, 427/126.3
• US Class Current: 501/12
• CPC Class Codes: C04B 2111/00801 Membranes; Diaphragms
• CPC Class Codes: C04B 35/46 based on titanium oxides or titanates containing also zirconium or hafnium oxides, zirconates or hafnates C04B35/49
• CPC Class Codes: C04B 38/0045 by a process involving the formation of a sol or a gel, e.g. sol-gel or precipitation processes

Abstract

A metal oxide particulate membrane is made more electrically conductive, and thus more suitable for electrochemical cells by the incorporation into the membrane of a dopant element. The dopant is dissolved in an alcohol and then incorporated in the sol-gel process used to form the particulate metal oxide membrane. The invention is exemplified by a niobium doped titanium dioxide ceramic membrane which has good porosity while having a conductivity several orders of magnitude higher than a similar membrane made without incorporating the niobium dopant.

Claims

1. A method of making a metal oxide ceramic membrane with improved conductivity comprising the steps of:

(a) dissolving in alcohol a quantity of a dopant element selected to have a valence value one different from the metal of the metal oxide ceramic;

(b) combining with the dissolved dopant a quantity of a metal alkoxide selected to give a preselected ratio metal to dopant in excess of ten to one in the resultant membrane;

(c) adding to the combination solution a limited amount of water and an acid in sufficient quantity to begin to peptize the metal oxide;

(d) slowly adding an additional quantity of water to the combination solution;

(e) heating the combination solution while stirring until a colloidal suspension is achieved;

(f) separating water from the colloidal suspension until a gel is made; and

(g) sintering the gel at a temperature of between about 200°

C. and 600°

C. into a unitary, durable, continuous porous ceramic membrane which then has incorporated into it the dopant element and which has an electrical conductivity of at least ten times higher than a porous ceramic membrane made without the dopant element.

2. The method of claim 1 wherein the metal alkoxide is in alcohol solution and wherein the alcohol in which the dopant is dissolved in a different alcohol from the alcohol in the metal alkoxide solution.

3. The method of claim 1 wherein the ratio of metal to dopant is between 100 and 10 to one.

4. The method of claim 1 wherein prior to step (c), the mixture is anhydrous.

5. The method of claim 1 wherein the sintering is at a temperature of 400 to 600 degrees C.

6. The method of claim 1 wherein the resultant membrane has conductivity at least one thousand times greater than the conductivity of a similar membrane prepared without the dopant being added.

7. The method of claim 1 wherein the dopant element has a valence value one more than the metal of the membrane.

8. A method of making a niobium doped titanium ceramic membrane comprising the steps of:

(a) dissolving in alcohol a quantity of a niobium slat;

(b) adding to the dissolved niobium salt a quantity of a titanium alkoxide, the quantity selected to give a molar ratio of between 10 and 100 of titanium to niobium in the solution;

(c) adding a limited amount of water and an acid to commence the peptizing of the titanium oxide molecules;

(d) diluting the combination with additional water and stirring to ensure complete mixing;

(e) heating the combination while stirring for a sufficient time for a colloidal suspension to form;

(f) dewatering the colloidal suspension to make a gel; and

(g) sintering the gel at a temperature of between about 200°

C. and 600°

C. to make a titanium oxide porous ceramic particulate membrane having a selected amount of niobium integrally incorporated into the membrane the membrane having an electrical conductivity of at least ten times higher than a porous ceramic membrane made without the niobium.

9. The method of claim 8 wherein the titanium alkoxide is dissolved in alcohol and wherein the alcohol in which the niobium is dissolved is a different alcohol from the alcohol in the titanium alkoxide.

10. The method of claim 9 wherein the alcohol in which the niobium is dissolved is ethanol and the titanium is tetraisopropoxide.

11. The method of claim 8 wherein prior to step (c), the mixture is anhydrous.

12. The method of claim 8 wherein the acid is hydrochloric acid.

13. The method of claim 8 wherein the sintering is at a temperature of 400 and 600 degrees C.

14. The method of claim 8 wherein the resultant membrane has conductivity at least one thousand times greater than the conductivity of a titanium oxide ceramic membrane prepared without the niobium being added.

15. A novel composition of matter comprising a titanium oxide particulate porous ceramic membrane having integrally incorporated into its particles doping atoms of niobium in amount such that the ratio of titanium to niobium is between 100 and 10 to one, wherein the membrane has an electrical conductivity at least ten times higher than a titanium oxide particulate membrane without the niobium doping and a surface area in excess of 50 square meters per gram.

16. A porous particulate metal oxide ceramic membrane in which a dopant is integrally incorporated in the particles of the metal oxide sintered into the membrane, the dopant selected to have a valence value one different from the metal and present at a concentration of less than 10% of the metal of the metal oxide the electrical conductivity of the metal oxide ceramic membrane being at least ten times higher than the electrical conductivity of a metal oxide membrane without the dopant, the porous ceramic membrane having a surface area in excess of 50 square meters per gram.