simmerman
Harmless
Posts: 3
Registered: 9-10-2013
Member Is Offline
Mood: No Mood
|
|
HCl + ?? = NH3 + ??
Hello,
I need to find a compound that frees ammonia in gas form when reacted with dry HCl. I've been searching but couldn't find any. Could anyone please
help me?
|
|
Fantasma4500
International Hazard
Posts: 1681
Registered: 12-12-2012
Location: Dysrope (aka europe)
Member Is Offline
Mood: dangerously practical
|
|
frees ammonia when reacted with HCl??
this sounds quite hard as acid vapours will react with the freshly formed NH3, if its even possible to do, and then make NH4Cl
i know that KNO3 + NaOH + Al = NH3
the hydrogen is coupled with the nitrogen from the KNO3, somehow.. quite interesting experiment.. however also ammonia salts reacted with a carbonate
or hydroxide will form (NH4)2CO3 (decomposes at 70*C IIRC into NH3 and CO2) and with hydroxide NH4OH which naturally decomposes from water (NH3*H2O
> NH3 + H2O)
what are you planning anyways?
|
|
deltaH
Dangerous source of unreferenced speculation
Posts: 1663
Registered: 30-9-2013
Location: South Africa
Member Is Offline
Mood: Heavily protonated
|
|
HCl + NaNH2 => NH3 + NaCl
NaNH2 = sodium amide.
[Edited on 9-10-2013 by deltaH]
|
|
bismuthate
National Hazard
Posts: 803
Registered: 28-9-2013
Location: the island of stability
Member Is Offline
Mood: self reacting
|
|
The ammonia would be mostly impure just mix NaOH with an ammonium salt and it will make ammonia.
|
|
bismuthate
National Hazard
Posts: 803
Registered: 28-9-2013
Location: the island of stability
Member Is Offline
Mood: self reacting
|
|
sorry. if you want to make it in the gas phase the first thing you need to worry about is your apparatus.
I recomend the method suggested by deltaH.
|
|
woelen
Super Administrator
Posts: 8014
Registered: 20-8-2005
Location: Netherlands
Member Is Offline
Mood: interested
|
|
@bismuthate: Please read more carefully what the OP wants. This is not a general question about making ammonia gas, this is a (most likely
theoretical) quest for a very special situation in which addition of HCl gas to a certain chemical gives NH3. DeltaH gives a perfect answer to this
question. No more explanation is needed.
Btw, in practice, I found a similar thing the other way around. Adding NH3 to a chemical can give HCl. If you add aqueous NH3 to TCCA, then you get N2
and HCl (material becomes strongly acidic) and other products, which in turn leads to formation of Cl2.
|
|
deltaH
Dangerous source of unreferenced speculation
Posts: 1663
Registered: 30-9-2013
Location: South Africa
Member Is Offline
Mood: Heavily protonated
|
|
Quote: | Btw, in practice, I found a similar thing the other way around. Adding NH3 to a chemical can give HCl. If you add aqueous NH3 to TCCA, then you get N2
and HCl (material becomes strongly acidic) and other products, which in turn leads to formation of Cl2. |
Interesting! I've always wanted to try a few things with TCCA, never had the pleasure of fiddling with it. I have however experimented extensively
with its cousins melamine and cyanuric acid!
[Edited on 9-10-2013 by deltaH]
|
|
bismuthate
National Hazard
Posts: 803
Registered: 28-9-2013
Location: the island of stability
Member Is Offline
Mood: self reacting
|
|
I belive magnesium nitride reacts with acids (and water) to make ammonia.
|
|
simmerman
Harmless
Posts: 3
Registered: 9-10-2013
Member Is Offline
Mood: No Mood
|
|
Thanks all for your answers.
In my (theoric) reaction, I got HCl as byproduct (which I need to neutralize), and as I need to react the product with ammonia, it will be nice to get
it produced rather than gassing it from an external aparatus.
Sodium amide proposed by deltaH seems to fit me, however it is a nasty chemical that I would like to avoid. Ayone knows any other option?
|
|
bfesser
|
Thread Moved 9-10-2013 at 05:00 |
WGTR
National Hazard
Posts: 971
Registered: 29-9-2013
Location: Online
Member Is Offline
Mood: Outline
|
|
Supposedly the "First commercial process using ionic liquids" was developed by BASF for the purpose of scavenging HCl from a reaction mixture. http://www.basf.com/group/corporate/en/innovations/publicati... . 1-methylimidazole is reacted with HCL to form 1-methylimidazolium chloride,
which separates as a separate liquid (at over 75°C) phase in non-polar solvents. The 1-methylimidazole can be reclaimed by reacting the chloride
salt with a base.
I realize that this doesn't produce ammonia, but maybe it will be of use to you.
[Edited on 9-10-2013 by WGTR]
|
|
bismuthate
National Hazard
Posts: 803
Registered: 28-9-2013
Location: the island of stability
Member Is Offline
Mood: self reacting
|
|
magesium nitride will make ammonia on contact with HCl. it is safer than sodium amide because instead of making caustic NaOH on contact with water it
makes rather harmless MgOH. I know that I already posted this, but I feel that this is safer.
|
|
deltaH
Dangerous source of unreferenced speculation
Posts: 1663
Registered: 30-9-2013
Location: South Africa
Member Is Offline
Mood: Heavily protonated
|
|
What about ammonium carbamate, its a really cheap salt made as an intermediate to urea and fairly safe (smells strongly of ammonia though), but the
down side is that it would produce ammonia and carbon dioxide, though maybe the CO2 is not a problem in the context of your needs?
The reaction would be:
NH4CO2NH2 + HCl => NH4Cl + NH3 + CO2
|
|
simmerman
Harmless
Posts: 3
Registered: 9-10-2013
Member Is Offline
Mood: No Mood
|
|
Great ideas guys, CO2 is not a problem. Thank you all!
|
|
deltaH
Dangerous source of unreferenced speculation
Posts: 1663
Registered: 30-9-2013
Location: South Africa
Member Is Offline
Mood: Heavily protonated
|
|
Pleasure, my consulting fee is $1000... just kidding... come again
|
|
deltaH
Dangerous source of unreferenced speculation
Posts: 1663
Registered: 30-9-2013
Location: South Africa
Member Is Offline
Mood: Heavily protonated
|
|
@bismuthate, you only get $100 'cause I need the money more lol
|
|
bismuthate
National Hazard
Posts: 803
Registered: 28-9-2013
Location: the island of stability
Member Is Offline
Mood: self reacting
|
|
Hey I though we agreed that i get 25%! nice idea ammonium bicarbonate is safe and
easy to find.
|
|
deltaH
Dangerous source of unreferenced speculation
Posts: 1663
Registered: 30-9-2013
Location: South Africa
Member Is Offline
Mood: Heavily protonated
|
|
ammonium bicarbonate wouldn't work though, that would just release carbon dioxide with no ammonia:
NH4HCO3 + HCl => NH4Cl + CO2 + H2O
ammonium carbamate is not the same thing, the carbamate ion has the looks like this: [O-CO-NH2]-
ok ok, I agree to 25% of $100
|
|
bismuthate
National Hazard
Posts: 803
Registered: 28-9-2013
Location: the island of stability
Member Is Offline
Mood: self reacting
|
|
sorry i messed up there however the heat of the reaction woul most likely decompose the bicarbonate. This would release ammonia I believe so there is
a nonchemical way to do this. (sorry I misread)
|
|
deltaH
Dangerous source of unreferenced speculation
Posts: 1663
Registered: 30-9-2013
Location: South Africa
Member Is Offline
Mood: Heavily protonated
|
|
No problems, I figured as much, I just wanted to make sure op wouldn't use bicarbonate instead of carbamate.
|
|