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Author: Subject: unconventional sodium
JJay
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[*] posted on 28-4-2017 at 00:22


Tomorrow, NurdRage is uploading his video on his new technique for making sodium. I can hardly wait.

C9-5eH0V0AALMqO.jpg - 292kB




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[*] posted on 28-4-2017 at 02:24


Woohoo!
I think I will buy a few hundred grams of Mg in readiness!
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[*] posted on 29-4-2017 at 05:20


And, If I am not mistaken, I think this is the definitive work.
https://www.youtube.com/watch?v=jCrFFVVcPUI

Kudos to Nurdrage for his efforts. This really is the most promising thing I have seen in... well ever. It looks so much tidier than electrolysis of molten NaOH or any other methods I have seen.
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JJay
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[*] posted on 29-4-2017 at 11:47


Definitely very cool. I am going to have to make some dioxane when I get my fume hood built.



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[*] posted on 9-6-2017 at 12:56


Likewise, JJ. Although I'll work outside for it instead and wear hazmat gear in place of the hood, for this, considering that the initiation of the magnesiothermic reduction is not something one would want indoors. Happen to have plenty antifreeze that was going to be used for making perc, during a time when no chlorocarbons were available, but now plenty dichlor is to hand when needed, less can go on to be chlorinated w/ Zn/HCl, trying Nurdrage's dioxane method for Na separation (and will try with KOH also), got everything needed to make a go at it, just as long as the antifreeze is ethylene glycol rather than DEG as is sometimes to be found. Although I think I picked up some EG specifically, about a gallon of the stuff.

This is a great discovery, my compliments to Nurdrage for this. Looks like it beats the absolute piss out of the various rather touchy electrolytic processes.

How prone is 1,4-dioxane to peroxidation compared with diethyl ether, diisopropyl ether, and THF? for longer term storage of a quantity of dioxane that would be dedicated to this particular purpose, storage over sodium after argon sparging and degassing under vacuum, followed by an argon blanket over any headspace in the 1,4-dioxane ought to reduce and eliminate peroxides as formed should it not? so if stored over a few nuggets of Na, can the dioxane not be continually recycled, since refluxing over Na (and the dioxane batch being dedicated specifically to magnesiothermic Na or K production), it would get regular treatment for peroxides as essentially a side bonus of the process itself taking care of any formed peroxides should it not?

And two other questions-what is the shelf-life of 1,4-dioxane inhibited with a little BHT or BHA, with or without sodium? And uninhibited dioxane if not otherwise treated, how long does significant peroxidation take, roughly?

Have you considered, after first pre-drying the dioxane, using an argon blanket over the liquid 1,4-dioxane and storage under Ar to increase shelf life?

And when using Mg powder (mine is, IIRC 400 mesh, possibly 500) how manageable is the reaction in comparison with that using Mg swarf/turnings? does the fine grain size not result in a dramatically faster, more energetic reduction of the caustic? I'd sooner nnt have any rapid deflagration/flashover when attempting this.

I noticed, nurdrage, that he distilled the dioxane to dryness. This is something that I have always had drilled into me, as something never to do with ethers, does this apply to freshly treated (immediately before use) ethers, when treated for peroxides and distilled under a current of inert gas. Ordinarily distilling ethers to dryness is or can be dangerous because any peroxides formed already are concentrated and can pose a significant hazard if present, since once concentrated down there is much less solvent to peroxide ratio, increasing the potential for a big mess that one really wouldn't want occurring in one's glassware, and less still doing so whilst the experimenter is within range of flying razor sharp glass fragments.
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[*] posted on 9-6-2017 at 19:18


I honestly can say that the risk if peroxides is almost zero if the peroxides are stored over a small amount of sodium and kept in a tightly sealed bottle. I use Boston round bottles (from Dr.Bob, no less!) to store the relatively small amount of peroxide I have, but really any airtight bottle should work. As for the speed of the reduction, once I tried burning sodium hydroxide with magnalium (before the whole NurdRage sodium process came out) and using 200-325 mesh magnalium and coarse to medium hydroxide, and it burnt hot and even after cooling, reacted vigorously with water. Therefore, I think that with very fine magnesium and powdered sodium, you will boil off some of your yield.
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[*] posted on 3-6-2018 at 12:40


This, no doubt, has been posted elsewhere.

Nurdrage has moved on, to an even more do-able Sodium Synthesis.

Not a thermite type reaction!

Just prolonged heating and stirring, with Magnesium, NaOH, a catalyst, and Baby oil.

https://www.youtube.com/watch?v=oiZf-O6vvbE

Kudos!
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[*] posted on 3-12-2019 at 04:28
Carry on with active metals...


Some time ago I have tried the thermite-type reaction to produce some sodium.
Some notes for the ones that would want to attempt this also:
- make sure that your reaction vessel will not melt, as a lot of heat is generated.
- make sure that you have a proper fire extinguishing equipment ready, just in case (additional pile of dry sand will also be handy, you can't be too careful).
- it's a good idea to dig your reaction vessel into the ground to prevent it from tipping over.
- sparklers should be enough to initiate the reaction.
- cover the vessel immediately with a heavy "lid". A brick should be fine.
- a huge fireball may happen anyway, so take away all flammable things from the reaction spot, including yourself.
- SERIOUSLY, DON'T EVEN THINK OF DOING IT INSIDE.
- bigger, un-crushed chunks of "slag" will decrease the yield. Dioxane separation requires small particles.
- it's a good idea to mix the dioxane with NaOH, let it sit for some time, destroy the peroxides and finally distill it. Ja=ust to make sure that it doesn't contain lots of water eager to decrese your yield further.
- it's also a good idea to dehydrate the oil you plan to store your sodium in.

And here are some coalescing sodium droplets:


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[*] posted on 26-5-2020 at 12:37


what if you decompose sodium azide in mineral oil since decomposition of sodium azide yields sodium metal as seen in a video by dbx labs.
https://www.youtube.com/watch?v=gZSfroJ1FJE&t=155s
seems a bit pointless since making sodium azide is not easy but still it may work
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[*] posted on 31-1-2021 at 12:36


some guy succesfully made sodium metal using sodium azide decomposition under mineral oil from this vid
https://www.youtube.com/watch?v=GMSzXdmTeBM
I predicted som1 would be mad enough to try this!!!
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[*] posted on 4-5-2022 at 06:55


I wonder if anyone has tried Nurdrages menthol-method but in a metal container, like stainless steel. There would of course be no glassware corrosion, and the whole thing could be built so that even if it does catch fire, nothing happens. It just needs to keep 200 or so degrees for 20-30 hours...

[Edited on 4-5-2022 by Jome]

[Edited on 4-5-2022 by Jome]
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Tsjerk
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[*] posted on 4-5-2022 at 08:41


There is no glass corrosion when you jump start the reaction with a bit of sodium. No water == no corrosion
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[*] posted on 4-5-2022 at 11:03


Sodium metal will probably corrode other metals by intercalation.



[Edited on 04-20-1969 by clearly_not_atara]
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[*] posted on 15-7-2022 at 12:19
Electrolysis of molten sodium formate


Reading through this thread there was at one point the idea of electrolyzing molten carboxylic acid salts of sodium. Aparrently this doesn't work with acetates or longer chain salts as those form some weird organic gunk.

However who said formate won't work? Ideally it would just loose the formate as CO(2) and water and deposit sodium on the cathode.
Long story short I tried that and it might just have worked. I used a graphite anode and an iron nail as the cathode. Now I didn't see actual metallic globules of sodium floating around but there were some yellow sparks close to the cathode every now and then. Unfortunately I couldn't quite keep the melt hot enough and my sodium formate definitely wasn't dry enough.

The solid that was stuck to the cathode also released quite a bit of H2 gas upon throwing it in water. This definitely looks promising to me so ig I'll try to optimize it a little this weekend.




Nothing much, just a few useful sites:

Find related papers: https://connectedpapers.com
Get those juicy papers: https://sci.hubg.org
Solubility data: https://chemister.ru/Database/search-en.php
Azeotrope data: http://azeotrope.info
ChemPlayer videos: https://archive.org/download/ChemPlayer
Organic Syntheses: http://orgsyn.org
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[*] posted on 25-7-2022 at 03:29


Well that didn't work. Some traces of sodium are produced but it seems to quickly react with the formate to give hydrogen and sodium carbonate. The carbonate quickly builds up on the cathode and stops the electrolysis. Also it's quite hard to keep the formate nice and molten without decomposing it to oxalate and hydrogen gas.



Nothing much, just a few useful sites:

Find related papers: https://connectedpapers.com
Get those juicy papers: https://sci.hubg.org
Solubility data: https://chemister.ru/Database/search-en.php
Azeotrope data: http://azeotrope.info
ChemPlayer videos: https://archive.org/download/ChemPlayer
Organic Syntheses: http://orgsyn.org
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