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Asontg
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- TL;DR Summary
- using a diaphragm electrolysis cell for a chloralkali process to produce koh using kcl
Hi everyone, I'm new on this forum, I make potassium soap but there were changes in the regulations in my country (Argentina) and now there's a lot of slow bureaucracy needed to buy chemicals like KOH (the regulations are industry-focused but are affecting small businesses like mine) so meanwhile I need a temporary solution which is to produce the KOH by myself through electrolysis
the idea is to use a diy diaphragm electrolysis cell for a chloralkali process, the catholite (with destilled water) and analyte (with a saturated solution of KCL), placing an inverted funnel on the anode and connecting it to a baker with NAOH to absorb most of the CL gas as this is very toxic, this might turn into bleach in the end. It will be necessary to stir the analyte often to make sure anode is always in contact with the saturated solution (this when the cell is turned on) in the case of the cathode, covering most of the chamber, not airtight, allowing some of the H gas to escape (this to prevent CO2 from getting into the chamber as it would react with the KOH) in a small scale this would be done with 1.5 amps for around 4 days and probably produce around 50 grams of KOH, in the end, the anode will still have KCL though contaminated with bleach and impurities, the cathode will have a solution with KOH. Titration will need to be performed in order to find out how much KOH is in that solution
Could this be scaled up to produce kilograms, not just a few grams? possibly using 2 of the typical 120 liters steel barrels? are there any other safety measures I should keep in mind? (besides wearing gloves, etc) specially with hydrogen being flammable. is there anything I might be missing? thanks beforehand
the idea is to use a diy diaphragm electrolysis cell for a chloralkali process, the catholite (with destilled water) and analyte (with a saturated solution of KCL), placing an inverted funnel on the anode and connecting it to a baker with NAOH to absorb most of the CL gas as this is very toxic, this might turn into bleach in the end. It will be necessary to stir the analyte often to make sure anode is always in contact with the saturated solution (this when the cell is turned on) in the case of the cathode, covering most of the chamber, not airtight, allowing some of the H gas to escape (this to prevent CO2 from getting into the chamber as it would react with the KOH) in a small scale this would be done with 1.5 amps for around 4 days and probably produce around 50 grams of KOH, in the end, the anode will still have KCL though contaminated with bleach and impurities, the cathode will have a solution with KOH. Titration will need to be performed in order to find out how much KOH is in that solution
Could this be scaled up to produce kilograms, not just a few grams? possibly using 2 of the typical 120 liters steel barrels? are there any other safety measures I should keep in mind? (besides wearing gloves, etc) specially with hydrogen being flammable. is there anything I might be missing? thanks beforehand