Potassium Chlorate

mrjeffy321

The concentration of the NaOCl in the bleach solution is by weight….it is 5% Sodium Hypochlorite by weight, not by moles / volume / ….
If we have 1 kg of 5% bleach, then that means that we have 50 grams of NaOCl and 950 grams of H2O.

Overflow

Oh, thanks for the clarification.
So the only way to know how many moles of NaClO is to actually weight the bleach?

Another couple questions:

-how do we know when the 3NaClO -> 2NaCl + NaClO3 reaction has completed (all NaClO converted, i don't even know if it's possibile!)

-will all the NaClO3 become KClO3, given enough KCl?

mrjeffy321

Or you could measure the volume of the bleach and calculate its mass using a known density.
It is a pretty safe assumption that the Sodium Hypochlorite has all decomposed after boiling off the large volume of water necessary to complete the procedure. If you start off with 1 liter of bleach, you will need to boil it down quite a bit (much less than half its original volume). This boiling process takes a lot of time usually and while this is happening, the NaOCl has plenty of time to decompose.

NaClO3 is very soluble in water. KClO3 is not very soluble in cold water (only a few grams per 100 mL). In order to form and collect KClO3 you are taking advantage of this difference in solubility. You start out with a solution of NaClO3 which is disassociated into ions (Na+, ClO3-), then you introduce another aqueous solution (of KCl) which contains K+ and Cl- ions. The K+ ions will “see” the ClO3- ions are a precipitation reaction will occur. The K+ and ClO3- will combine to form KClO3 which will quickly saturate the solution and then precipitate out as a solid. In the end, there will still be some small amount of K+ and ClO3- ions left over in solution, plus plenty of Na+ and Cl-, there is nothing you can do about this except try to make the conditions are favorable as possible for the KClO3 precipitate to form.

Overflow

Known density... uhm, where should i look? :P

Yeah, i boil it to 150ml.
I'd immagine a lower heat (electric plate) would give more time for the reaction to happen than a high heat (gas burner), right?

Two days ago i created my first batch with this method and got something that surely had some chlorate (it burned quite fiercely mixed with sugar) but also a lot of sodium.
So yesterday i went to purify this stuff, with a boil + filter action :)
The weird thing is that the chlorate had deposited on the bottom of the pyrex container and as soon as enough heat was there it started to "explode", with little escapes of oxygen!
Now it seems i just lost all the chlorate, as the white powder that deposited was totally unreactive, my guess is that having not well mixed the chlorate with the water the chlorated decomposed into something else
Ideas?

Squall

If you are trying to make chlorate i would go the electrolysis way. It might take a little longer and require a some work, but the results you get are a whole lot better thah boiling bleach. i a m actually working on a new cell design at the moment. If you are interested i could share my luck with it.
And remember always be careful with chlorate.

Overflow

Very interested, sent you PM :)

rashean123

success!!!!

ive finally got some chlorate when freezing the solution, after weeks of failure i managed to get about 412-414 grams, i tested it with sugar and it made a bright purple flame that seem to flash when i lit, it.


is this really potassium chlorate or is it another failure








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its free

mrjeffy321

Excellent! Purple is the magic color...it lets you know that you have removed almost all of the Sodium impurities. How many crystalizations did you do to get it to this level, or did it just come out this way on the first try?
It sounds like you were very successful. It obviously behaves as KClO3 should and the purple flame indicates the Potassium ion is present without a significant amount of Sodium (the Sodium's yellow color will easily overpower other, weaker, colors like the purple from Potassium).


As long as we are sharing results with each other.....
just last week I finished what currently holds the record for my largest electrolytic Chlorate cell to date.
I electrolysized about 800 grams of Sodium Chloride over the course of about 2 weeks to make (theoretically) about 1000 grams of Sodium Chlorate.
When I precipitated out the KClO3 from solution and dried it, I measured its mass to be about 850 grams. Although it is far from the theoretical yield (since there is probably about 100 or so grams left in solution which I cannot easily extract), I am still quite happy with it. it appears to be of excellent quality, although I have not tested it (no need really, I know what it is just by looking at it...I know what the crystals should look like by now). After drying it, I re-dissolved it in boiling water along with a little remaining ("dirty") Chlorate I had sitting around. I precipitated all of this out of solution again and it is currently drying (and will do so for the next 2 months while I am away from home).
This most recent Chlorate cell run has gave me another milestone....I did not have any majors accidents while running it. It seems, as luck has it, I always do something to screw up my cells runs (either knock it over with my hand, connect the electrodes up reversed, ...), but this time everything went reasonably smoothly.

During the run I employed the use of my Amp Hour meter (to measure the charge put through the cell) and a new digital pH probe to make twice-daily pH adjustments. The cathode was a single, threaded, stainless steel rod placed in the center of the lid of a plastic container and was surrounded by Carbon-graphite rods (as the anodes) placed in a 2-layer, circular, pattern around the cathode.

rashean123

it pretty much came out this way, i thought ide do one last try at it and it finally worked.
wow! 800-1000 grams, what was your cell voltage?, and have you ever had any heat problems? with the cell, and does the cell have to work at a certain temp?, and how do you tell if its sodium chlorate ?, because think it wont burn the same.






lol too many questions

mrjeffy321

My cell voltage was around 5 volts.

Yes, when running so much current through the cell for extended periods of time a lot of heat does build up. This most recent run cycle was not too bad since I was only consuming about 50 watts or so of power, but never-the-less the electrolyte solution did get warm after a while.
On a previous run cycle I was consuming about 80-90 watts of power and heat was a much bigger problem as much of the plastic/rubber insulation on the wires and aligator clips was melting. At one point, I placed a small resistor into the circuit to help lower the current and dissipate some power. This resistor was not up to the job and practivally burned itself out and overheated. I tried freezing the resistor in a block of ice and then insulating the ice from the cell running environment. After not too long I would come back and check the cell and my block of ice had turned into a pool of hot water.

There is an ideal temperature range to opperate the cell in which the Chlorate production becomes the most efficient. This temperature is somewhere around 70-80 degrees C I think, but precise temperature control is hardly necesary I think. As I said already, the power dissipated by the cell (as it acts like a resistor in the circuit) will keep the electrolte very warm (possibly even too warm).

You know you have produced NaClO3 is you add some KCl to it and get a precipitate. If the precipiate burns when mixed with a fuel (sugar), it is KClO3.
NaClO3 burns in a very similar manner to KClO3.

rashean123

oh and how much water did u use ?

rashean123

what power source did you use, like a better charger or.....?

rashean123

oh and thx 4 the response

mrjeffy321

The volume of my electrolyte solution was about 2.5 Liters.

As a power source, I used a converted computer ATX power supply. I connected the +5 volt and Ground terminals across my cell.
A long time ago, when I was just starting, I would use battery chargers as a power source, but you cannot draw much current from them without burning them out so I really needed to upgrade to the power supply I have now.

I haven been through many cell designs over the years (I think there is information about this in my Potassium Chlorate thread, maybe). But I need to figure out a better design before I will try to do another run, so it will likely be a while.

rashean123

ohh, well i have made my chlorate but i will keep it for experimental uses 4 now, considering i do not want anything to go wrong 4 this years fireworks display.

oh and do you make ur own firewors(ball shells, canisters,mines,cakes), or do you buy them.






just wanted 2 know

mrjeffy321

Surprisingly.....neither.
I am forced to be content with merely watching the city’s firework display when the 4th of July rolls around.

rashean123

OOOOhhhhh ok