Daffodile
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Failure to isolate Calcium Cyanate
Hey guys, just hoping for an explanation or insight into why my procedure isn't working.
I'm attempting to make pure calcium cyanate, so I did the urea/ sodium carbonate melt to collect a product of solid off-white sodium cyanate.
To remove contaminants such as sodium carbonate, the crude sodium cyanate was dissolved in 50% hot acetic acid.
The resulting solution was then mixed with aqueous calcium chloride, expected was the calcium cyanate product.
Instead I have nothing. Does anyone have suggestions for why this might not be working?
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Metacelsus
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The acid step might have decomposed your cyanate. It's known to hydrolyze to carbon dioxide and ammonia under acidic conditions, especially when hot.
I think adding acid to remove the carbonate is OK as long as you don't add excess acid. Carefully monitor the pH and make sure the solution doesn't
become acidic.
[Edited on 2019-3-17 by Metacelsus]
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draculic acid69
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Adding acid to sodium cyanate will decompose it when hot for sure it's also a terrible way to purify it,you need to dissolve in hot water and add
ethanol and let the plates that form precipitate and then filter I forget the amounts of water/ethanol to naocn but it's in the literature somewhere
I've done it this way many times to purify the rxn products of sodium carbonate and cyanuric acid.its a low yeilding procedure so next time I'll use
urea instead I reckon it will give a better result.ill try NaOH instead of carbonate and try to capture the nh3 byproduct which comes off as the
carbonate which is harder to capture.all in all acids are not a great way to purify this substance.
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CharlieA
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Daffodile: Do you have a literature reference for this reaction, by any chance?
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Daffodile
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Which one?
The Urea decomposition is fairly common knowledge (ie: https://www.sciencedirect.com/science/article/abs/pii/S00406...).
More details on formation of Calcium Cyanurate here: http://www.sciencemadness.org/scipics/Engager/TzOTC/Syntheti...
Also: https://patents.google.com/patent/US3173755
It looks like free cyanic acid polymerizes pretty fast? Not really relevant but anyway. The acetic acid addition was my own idea, since I thought it
would dissolve all the contaminants mentioned in the patent without affecting the cyanate/ cyanurate. Maybe the desired product is too soluble to
precipitate? I am unable to find a literature Ksp value but I assumed it was pretty low. On second thought I was probably wrong and the calcium
cyanate/ cyanurate is decently soluble considering the properties of similar salts.
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draculic acid69
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Sodium cyanate is water soluble but not very .11.6g in 100 ml.
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