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Author: Subject: Need potassium chlorate cell advice
frozenstate
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[*] posted on 20-7-2017 at 12:01
Need potassium chlorate cell advice


I have been recently planning to setup a chlorate cell for electrolysis of potassium chloride to potassium chlorate, but I have found conflicting information and was wondering if anyone could give some pointers before I actually start construction of my cell.

I plan on using a standard 2-5 gallon plastic bucket made of HDPE polyethylene (for chemical resistance), and drilling 3 holes in the lid: 2 for cathode/anode, the last used for venting gases. The anode I plan to use is MMO mixed metal and the cathode would be a stainless steel rod. I plan to space the anode/cathode about 2-3 inches away from each other, and have them placed in in the center of the bucket lid.

Now from what I've seen online, it seems like most people prefer to use glassware as the storage container. Since polyethylene plastic is resistant to the chemicals used in this electrolytic process, would it be a good alternative? Also would appreciate if anyone can point out any possible design flaws.

Now here is where I get tripped up the most, the power supply.

It seems like its universally accepted that no more than 6V should be used for a chlorate cell without starting to risk anode/cathode corrosion damage over time.

Amperage / Current values however seem to be all over the place. I've seen some people use as low as 2 amps (cold cell) and up to 50 amps in some setups. I assume more amps = higher temps, so I probably wouldn't want to use too high temps especially around plastic right? Would 2 amps be good enough for my setup, or would I need more?

[Edited on 20-7-2017 by frozenstate]
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hissingnoise
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[*] posted on 21-7-2017 at 08:02


This should get you up and running...

http://www.oocities.org/capecanaveral/campus/5361/chlorate/c...

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XeonTheMGPony
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[*] posted on 22-7-2017 at 10:08


That link comes up as malicious ensure your spy ware scanner and antivirus is up to date!
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markx
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[*] posted on 26-7-2017 at 01:45



A plastic container made out of HDPE will work fine for the purpose of chlorate electrosynthesis, but very often they are not transparent, so you will have difficulty observing what happens inside the reactor. I must say it is quite pleasing to be able to observe the electrochemical reactions in the chlorate cell and witness the formation of first visible cristals (if one uses KCl as the starting material) :) Hence a glass container is visually more satisfying....also the temperature acpect should be taken into consideration when using plastic. I've used 5L PET water bottles as the reactor for chlorate production and it holds up just fine and is transparent, but one has to control the temperature of the electrolyte to keep the reactor from not shrinking down and deforming due to excessive heat. In that sense a glass vessel is more sturdy and durable....as long as you do not drop it or shock cool it. If you plan on using low current (below 10A) in a rather large vessel (several gallons) then the temperature aspect is negligible, but be prepared to run this thing for a duration of weeks to produce a considerable amount of product. Production rate is directly proportional to the current that the cell is running at.

As for the power supply a standard switchmode device with 5V nominal output rating is absolutely perfect. But it should be able to handle a fair amount of current and preferably have a means to regulate the output voltage in a reasonable range (3-5,5V e.g). Most standard switchmode power supplies have a small potentiometer for exactly that purpose and it really comes in handy for limiting of current during chlorate electosynthesis.
As for electrode damage (anode damage that is), it is not the particular voltage or current that the cell is run at that do the damage, but the "current density [A/surface area]" at the anode surface that , when exceeding a critical value, will cause the anode to deteriorate. For practical purposes at the cathode there is no critical current density that can cause damage....the only thing that can happen is that the rate of ion transportation becomes limiting at the cathode surface above a certain current density and promote sidereactions (like the reduction of chlorate back to chloride). But for the anode one has to watch out to stay in the safe current density region. That means that one has to know the active surface area of the anode and the safe region for current density for the particular material that one uses as the anode (gaphite, MMO, noble metals, magnetite, lead dioxide etc.) In light of that it is benficial to use larger electrodes in the cell. For generic MMO (but keep in mind that there are several different kinds out there) the safe current density lies usually below 0,2A/cm2.....that means that for example a cell with a MMO anode having an active surface area of 100cm2 is good to run for at a maximum of 20A current. And it really does not matter how one achieves that current through the cell, it can be done with the help of a 12V battery charger or with a designated 5V power supply....either way if one goes over the 20A limit for extended periods of time the anode will be cooked. Another thing to watch out for are contaminants in either the chloride salt or the water that one uses to prepare the cell liqour. It is safer to use deionised water and food grade chlorides, but I have used fertiliser grade KCl and regular tap water with great success on both graphite and MMO anodes....so your mileage may vary :)
As for the placement and geometry of electrodes I would suggest to use two flat plates of stainless steel for the cathode and and a MMO anode of equal dimensions sandwitched between the cathode plates with about an inch of equal clearance between them. That enables both sides of the anode mesh to work equally and balance the system, but a single plate anode and cathode facing each other will work too and are less complicated to fabricate.



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Exact science is a figment of imagination.......
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symboom
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[*] posted on 13-9-2017 at 23:34


keeping with the diy anode any ideas of anode from a large Tantalum capacitor it seems to have similar properties of titanium except its oxide layer is conductive could this be used



Natures Intellectual Organic Peroxide. >>Ascaridole <<

Oxone
Used for the production of --> CH2O/Cl2/ClO2/Br2/I2

------------------------------------->>Hydrogen Peroxide << -------------------------------------------- >> Acetylene <<
Peroxide Salts
Zinc Peroxide <\> Copper Peroxide <\>Silver Peroxide <\>Lithium Peroxide <\>Magnesium Peroxide <\>Calcium Peroxide to Calcium Superoxide
CoO2. \\ NiO2 \\ Ti/V/Cr peroxy complex \\ Triamine chromium peroxide \\ LiH \\SiO2-H2SO4 (SSA) \\ [Ni(NH3)6]

Exotic reducing agents
Ga2O TiCl2 GeCl2 && Na2S2O4
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Varmint
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[*] posted on 14-9-2017 at 13:01


No idea if the OP is even watching this thread, but one key element of a good chlorate cell (that is not PH managed by HCL additions), is to have the cathodes much smaller than the anodes.

My cells use 76x76mm MMO anodes, with (2) 5mm dia. grade 2 (CP) titanium rods placed either side of the anode. Spacing is 30mm.

The chambers themselves are 2L beakers, and the top/electrode holder is from a 150mm PVC cylinder I turned and parted off on the lathe.

I run (4) cells in series, powered by a 24V @ 8A switchmode power supply, and I use a LM138K on a large heatsink with fan to form a constant current source of 5A.

The cells are placed in a Styrofoam "cooler" so the heat created builds up to about 60C. The temperature is roughly regulated by a servo motor controlled by an Arduino that raises the lid to allow cool air exchange. This is a dumb controller at this point, if I felt the temp control needed to be better I'd put some PID code in the Arduino, but it works fine as is.

Currently I only collect and discard the cell gasses with a manifold connected to a weak venture effect purge to outside. If I decide to run another batch, I'd like to include a means for collecting the anode and cathode gasses separately, they might be useful for further experiments.
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