MULTI-CELL COx ELECTROLYZER STACKS
US-2024060194-A1 · Feb 22, 2024 · US
US9663866B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9663866-B2 |
| Application number | US-201213486089-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jun 1, 2012 |
| Priority date | Dec 3, 2009 |
| Publication date | May 30, 2017 |
| Grant date | May 30, 2017 |
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The invention relates to a cathode for electrolytic processes provided with a catalytic coating based on ruthenium crystallites with highly controlled size falling in a range of 1-10 nm. The coating can be produced by physical vapor deposition of a ruthenium or ruthenium oxide layer.
Opening claim text (preview).
What we claim is: 1. Method of deposition of a porous separator on a cathode body of a diaphragm electrolytic cell, comprising: immersing the cathode body into a deposition vessel containing a suspension comprising polymer fibers and an optional particulate material; detecting a suspension level of the suspension in the deposition vessel using a level sensor; detecting a vacuum level in the deposition vessel; vacuum sucking the suspension containing polymer fibers and the optional particulate material through the cathode body by continuously adjusting the degree of vacuum applied as a function of the weight % of deposited fiber with respect to a predetermined total amount of deposited fiber wherein the weight % is calculated from a variation of the suspension level detected from the level sensor; obtaining a predetermined porous separator profile on the cathode body at the end of the deposition, wherein the obtained porous separator comprises a superposition of a multiplicity of polymer fiber planes comprising primary pores generated by the interconnection of a multiplicity of primary interstices between the fibers, the primary pores having an average value of about 2 to 10 microns. 2. The method according to claim 1 , wherein at the end of the deposition the method further comprises extracting the cathode body with the applied diaphragm and maintaining a degree of vacuum not lower than the degree of vacuum at the end of the deposition for a time of about 0.5 hours to about 3 hours. 3. The method according to claim 1 , wherein the degree of vacuum applied during the deposition reaches a maximum value of about 300 mm to about 650 mm Hg .
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