Diaphragm for electrolytic cell
View Patent ↗Describes a diaphragm for an electrolytic diaphragm cell, e.g., a chlor-alkali cell, in which the diaphragm comprises fibrous material substantially resistant to the environment within the electrolytic cell and spheroidal ceramic microspheres at least partially resistant to the environment within the electrolytic cell associated with said diaphragm. Also describes a diaphragm for an electrolytic cell in which the diaphragm comprises a base mat of fibrous material chosen from asbestos fibers, resin-modified asbestos fibers, synthetic fibers, or mixtures of such fibers on which base mat is applied a coating comprising spheroidal ceramic microspheres. Further describes a synthetic diaphragm for an electrolytic cell, e.g., a chlor-alkali cell, on which is applied a coating comprising substantially water-insoluble inorganic particulate material, e.g., clay material, and spheroidal ceramic microspheres. Still further describes adding a dopant composition comprising spheroidal ceramic microspheres to the anolyte compartment of an electrolytic cell, e.g., a chlor-alkali cell, while the cell is operating.
1. A method for reducing the permeability of a microporous liquid-permeable diaphragm of an electrolytic diaphragm cell comprising an anolyte compartment, a catholyte compartment and a liquid-permeable diaphragm, said diaphragm separating the catholyte compartment from the anolyte compartment and comprising a base of fibrous material substantially resistant to the environment within the electrolytic cell, which method comprises adding to the anolyte compartment particles of spheroidal ceramic microspheres that are at least partially resistant to the environment within the electrolytic cell, said microsphere particles (a) being used in an amount and (b) having a nominal size distribution that are sufficient to reduce the permeability of the liquid permeable diaphragm.
2. The method of claim 1 wherein the spheroidal ceramic microspheres are particles comprising at least one metal oxide chosen from the oxides of the metals zirconium, titanium, hafnium, silicon, aluminum, boron, vanadium, niobium, tantalum, molybdenum, chromium, tungsten, iron, cobalt, nickel, copper, zinc, cadmium, cerium, lanthanum, yttrium, beryllium, calcium, magnesium, tin, lead, gallium, germanium or mixtures of such metal oxides.
3. The method of claim 1 wherein the spheroidal ceramic microspheres are particles comprising at least one metal oxide chosen from the oxides of the metals silicon, aluminum, titanium, zirconium, boron, chromium, iron, calcium, magnesium, tin, zinc or mixtures of such metal oxides.
4. The method of claim 1 wherein the amount of spheroidal ceramic microspheres added to the anolyte compartment ranges from 0.1 to 10 grams per square foot of effective diaphragm surface area.
5. The method of claim 1 wherein the spheroidal ceramic microspheres have a nominal size distribution in the range of from 0.3 to 300 microns.
6. The method of claim 1 wherein the spheroidal ceramic microspheres have a nominal size distribution in the range of from 0.3 to 200 microns.
7. The method of claim 1 wherein the spheroidal ceramic microspheres have a nominal particle size within the range of from 1 to 40 microns.
8. The method of claim 1 wherein the spheroidal ceramic microspheres have a nominal particle size within the range of from 4 to 20 microns.
9. A method for reducing the permeability of a microporous liquid-permeable diaphragm of a chlor-alkali electrolytic diaphragm cell comprising an anolyte compartment, a catholyte compartment and a liquid-permeable diaphragm, said diaphragm separating the catholyte compartment from the anolyte compartment and comprising a base of fibrous material substantially resistant to the environment within the electrolytic cell, which method comprises adding to the anolyte compartment particles of spheroidal ceramic microspheres that are at least partially resistant to the environment within the electrolytic cell, said microsphere particles comprising at least one metal oxide chosen from the oxides of the metals silicon, aluminum, titanium, zirconium, boron, chromium, iron, calcium, magnesium, tin, zinc or mixtures of such metal oxides and (a) being used in an amount and (b) having a nominal size distribution which are sufficient to reduce the permeability of the liquid permeable diaphragm.
10. The method of claim 9 wherein the microporous liquid-permeable diaphragm is a synthetic diaphragm.
11. The method of claim 10 wherein the amount of spheroidal ceramic microspheres added to the anolyte compartment ranges from 0.3 to 8.5 grams per square foot of effective diaphragm surface area.
12. The method of claim 11 wherein the spheroidal ceramic microspheres are added to the anolyte compartment while the electrolytic cell is operating.
13. The method of claim 12 wherein the spheroidal ceramic microspheres have a nominal size distribution in the range of from 0.3 to 300 microns and a nominal particle size within the range of from 1 to 40 microns.
14. The method of claim 12 wherein the spheroidal ceramic microspheres have a nominal size distribution in the range of from 0.3 to 200 microns and a nominal particle size within the range of from 4 to 20 microns.
15. A method for reducing the permeability of a microporous liquid-permeable diaphragm of a chlor-alkali electrolytic diaphragm cell comprising an anolyte compartment, a catholyte compartment and a synthetic liquid-permeable diaphragm, said diaphragm separating the catholyte compartment from the anolyte compartment and comprising a base of fibrous material substantially resistant to the environment within the electrolytic cell, which method comprises adding to the anolyte compartment while the electrolytic cell is operating from 0.3 to 8.5 grams per square foot of effective diaphragm surface area of spheroidal ceramic microsphere particles that are at least partially resistant to the environment within the electrolytic cell, said ceramic microsphere particles comprising at least one metal oxide chosen from the oxides of the metals silicon, aluminum, titanium, zirconium, boron, chromium, iron, calcium, magnesium, tin, zinc or mixtures of such metal oxides, said ceramic microsphere particles having a nominal size distribution within the range of 0.3 to 300 microns, the amount and size distribution of said ceramic microsphere particles being sufficient to reduce the permeability of the liquid permeable diaphragm.
16. The method of claim 15 wherein at least one other material chosen from clay minerals, ceramic fibers, valve metal oxide, alkaline earth metal oxides/hydroxides, and fibers comprising halogen-containing polymers are added to the anolyte compartment in conjunction with the spheroidal ceramic microspheres.
17. The method of claim 16 wherein a material chosen from clay minerals, alkaline earth metal oxides/hydroxides, fibers comprising halogen-containing polymers, and mixtures of such materials are added to the anolyte compartment in conjunction with the spheroidal ceramic microspheres, and the ceramic microspheres represent from 5 to 100 percent of the material added to the anolyte compartment to reduce the permeability of the diaphragm.
18. The method of claim 17 wherein the spheroidal ceramic microspheres have a nominal size distribution in the range of from 0.3 to 200 microns and a nominal particle size within the range of from 4 to 20 microns.
19. A method of associating spheroidal ceramic microspheres with a microporous liquid-permeable diaphragm structure of an electrolytic diaphragm cell comprising an anolyte compartment, a catholyte compartment and a diaphragm structure separating the catholyte compartment from the anolyte compartment, said diaphragm structure comprising a foraminous metal cathode to which is adhered a base of fibrous material substantially resistant to the environment within the electrolytic cell and on which base is applied at least one coating of substantially water-insoluble inorganic particulate material, which method comprises adding to the anolyte compartment spheroidal ceramic microspheres that are at least partially resistant to the environment within the electrolytic diaphragm cell, thereby to associate said spheroidal ceramic microspheres with the diaphragm structure, said spheroidal ceramic microspheres having a nominal size distribution and being added in amounts that are sufficient to reduce the permeability of the liquid permeable diaphragm.
20. The method of claim 19 wherein the spheroidal ceramic microspheres are particles comprising at least one metal oxide chosen from the oxides of the metals zirconium, titanium, hafnium, silicon, aluminum, boron, vanadium, niobium, tantalum, molybdenum, chromium, tungsten, iron, cobalt, nickel, copper, zinc, cadmium, cerium, lanthanum, yttrium, beryllium, calcium, magnesium, tin, lead, gallium, and germanium.
21. The method of claim 19 wherein the spheroidal ceramic microspheres comprise at least one metal oxide chosen from the oxides of the metals silicon, aluminum, titanium, zirconium, boron, chromium, iron, calcium, magnesium, tin and zinc.
22. The method of claim 19 wherein the amount of spheroidal ceramic microspheres added to the anolyte compartment ranges from 0.1 to 10 grams per square foot of effective diaphragm surface area.
23. The method of claim 19 wherein the spheroidal ceramic microspheres have a nominal size distribution in the range of from 0.3 to 300 microns.
24. The method of claim 19 wherein the spheroidal ceramic microspheres have a nominal size distribution in the range of from 0.3 to 200 microns.
25. The method of claim 19 wherein the spheroidal ceramic microspheres have a nominal particle size within the range of from 1 to 40 microns.
26. The method of claim 19 wherein the spheroidal ceramic microspheres have a nominal particle size within the range of from 4 to 20 microns.
27. A method of associating spheroidal ceramic microspheres with a microporous liquid-permeable diaphragm structure of a chlor-alkali electrolytic diaphragm cell comprising an anolyte compartment, a catholyte compartment and a liquid-permeable diaphragm structure separating the catholyte compartment from the anolyte compartment, said diaphragm structure comprising a foraminous metal cathode to which is adhered a base of fibrous material substantially resistant to the environment within the electrolytic cell and on which base is applied at least one coating of substantially water-insoluble inorganic particulate material, which method comprises adding to the anolyte compartment spheroidal ceramic microspheres that are at Least partially resistant to the environment within the electrolytic cell, said spheroidal ceramic microspheres comprising at least one metal oxide chosen from the oxides of the metals silicon, aluminum, titanium, zirconium, boron, chromium, iron, calcium, magnesium, tin and zinc, said spheroidal ceramic microspheres having a nominal size distribution and being added in amounts that are sufficient to reduce the permeability of the liquid permeable diaphragm.
28. The method of claim 27 wherein the microporous liquid-permeable diaphragm is a synthetic diaphragm.
29. The method of claim 28 wherein the amount of spheroidal ceramic microspheres added to the anolyte compartment ranges from 0.3 to 8.5 grams per square foot of effective diaphragm surface area.
30. The method of claim 29 wherein the spheroidal ceramic microspheres are added to the anolyte compartment while the electrolytic cell is operating.
31. The method of claim 30 wherein the spheroidal ceramic microspheres have a nominal size distribution in the range of from 0.3 to 300 microns and a nominal particle size within the range of from 1 to 40 microns.
32. The method of claim 30 wherein the spheroidal ceramic microspheres have a nominal size distribution in the range of from 0.3 to 200 microns and a nominal particle size within the range of from 4 to 20 microns.
33. A method of associating spheroidal ceramic microspheres with a microporous liquid-permeable diaphragm structure of a chlor-alkali electrolytic diaphragm cell comprising an anolyte compartment, a catholyte compartment and a liquid-permeable diaphragm structure separating the catholyte compartment from the anolyte compartment, said diaphragm structure comprising a foraminous metal cathode to which is adhered a base of fibrous synthetic material substantially resistant to the environment within the electrolytic cell and on which base is applied at least one coating of substantially water-insoluble inorganic particulate material, which method comprises adding to the anolyte compartment while the electrolytic cell is operating from 0.3 to 8.5 grams per square foot of effective diaphragm surface area of spheroidal ceramic microspheres that are at least partially resistant to the environment within the electrolytic cell, said spheroidal ceramic microspheres comprising at least one metal oxide chosen from the oxides of the metals silicon, aluminum, titanium, zirconium, boron, chromium, iron, calcium, magnesium, tin, and zinc, said ceramic microspheres having a nominal size distribution within the range of 0.3 to 300 microns, the amount and size distribution of the spheroidal ceramic microspheres added to the anolyte compartment being sufficient to reduce the permeability of the liquid permeable diaphragm.
34. The method of claim 33 wherein at least one other material chosen from clay minerals, ceramic fibers, valve metal oxide, alkaline earth metal oxides/hydroxides, and fibers comprising halogen-containing polymers are added to the anolyte compartment in conjunction with the spheroidal ceramic microspheres.
35. The method of claim 34 wherein a material chosen from clay minerals, alkaline earth metal oxides/hydroxides, fibers comprising halogen-containing polymers, and mixtures of such materials are added to the anolyte compartment in conjunction with the spheroidal ceramic microspheres, and the spheroidal ceramic microspheres represent from 5 to 100 percent of the material added to the anolyte compartment to reduce the permeability of the diaphragm.
36. The method of claim 35 wherein the spheroidal ceramic microspheres have a nominal size distribution in the range of from 0.3 to 200 microns and a nominal particle size within the range of from 4 to 20 microns.