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NH4Cl > NH3 + HCl?


Theophrastus

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With a little thought, I made a sudden epiphany recently, in noticing that ammonium chloride (NH4Cl), can actually be split into two separate chemicals, NH3, and HCl. I thought of various methods, how this can be done, however, in ionising, the salt does not form the compounds above, but rather ammonium ion (NH4+) and chlorine ion (Cl-). Is there any way perhaps, to coerce this salt to decompose in the compounds described above, and how can this be done, without having the two products react, to form ammonia salt again. Any ideas?

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interesting problem

electrolysing probably won't work, it will probably get you

2NH4Cl > 2NH3 + H2 + Cl2

 

BAD idea. This nets you NCl3, a very powerful, dangerous, and unstable compound. Think NI3, but liquid and not safe when wet.

 

You can get one or the other out, but not both at once. Either use H2SO4 for the HCl or use NaOH solution for the NH3.

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oh, right...

thats how NI3 is made...

 

so not only would it not work, but unless you keep the chlorine and ammonia seperate, youll get dangerous chloramines :(


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in fact thats the main way to produce NCl3 nowadays

http://www.chm.bris.ac.uk/motm/ni3/ni3c.htm

 

i should probably learn a bit more chemistry before suggesting such ideas :P

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It decomposes that way if you heat it.

 

Thank you, I was simply making sure, however, I was thinking, what is the precise decomposition temperature for NH4Cl, because I was thinking, that if there is enough of a range between the boiling points of its two components, ammonia, and HCl, I suppose I could funnel the ammonia, into water, where it would dissolve, forming an ammonia solution, (hopefully) leaving the HCl, in the previous flask. Something along the lines of a basic distillation. Any thoughts?

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well you could always get HCl by reacting NH4Cl with a stronger acid, i.e. H2SO4, but then you might as well use table salt instead of ammonium chloride...

 

you can get NH3 by reacting NH4Cl with almost any base, i.e. react it with baking soda to make ammonium carbonate, which decomposes with only a little heat...

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you know, actually, if you gently electrolyse, the ammonia produced at the cathode can dissolve back into the water faster than it is generated. i think ammonia dissolves easier then chlorine, since Cl2 exists in equilibrium with HCl and HOCl... but at worst for every two steps forward of seperating NH4Cl, you'll be taking one step back of reformulating it...

 

this will eventually give you NH4OH solution, with a trace of NH4Cl... But thats basically the NH3 part...

 

the gases that do escape will be hydrogen and chlorine (with some ammonia and oxygen)... you can collect them and a match or spark will turn them back into hydrogen chloride... with some ammonium chloride, water, and NCl3:eek:...

 

you can leave it as HCl or maybe bubble it into water to get hydrochloric acid... But thats basically the HCl part.


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actually i guess NH3 also exists in equilibrium with NH4OH...

 

none the less, you can use even a very slight difference in solubility to seperate them...

 

and you can, for example, put one electrode in the bottom of the solution, and one almost on the surface, so that one of these- Cl2 or NH3- can dissolve easier...

 

and the ammonium chloride produced would just be electrolysed again... only thing is that if you let chlorine dissolve, you would also get HOCl with the HCl... i dont know if they are easy to seperate...

 

At least half of this is nonsense. If you electrolyze NH4Cl, you will make plenty of NCl3. Any NCl3 at all is too much. End of discussion, unless you'd like someone to seriously hurt themselves trying any of this.

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