Solubility of Sodium nitrate and nitrite

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The discussion centers on the solubility of sodium nitrate (NaNO3) and sodium nitrite (NaNO2), with a focus on the reliability of available data. It is noted that while literature suggests NaNO3 is slightly more soluble than NaNO2, practical experiments show NaNO3 crystallizing out first during separation processes. This raises questions about the accuracy of solubility data, particularly in highly concentrated mixtures where ionic strength can affect solubility behavior. Participants highlight that solubility values typically apply to single compounds and may not be applicable in mixtures. The conversation also touches on the idea that in solutions with similar solubility, the compound present in higher concentration may remain in solution longer, although this is not guaranteed. Overall, the discussion emphasizes the complexities of solubility in concentrated solutions and the potential for unexpected outcomes in crystallization processes.
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Hi, I wonder if anyone can share some info in regards to the reliability of the data that's available on the internet about the solubility of NaNO3 and NaNO2.
Everything I've found so far seems to point towards the nitrate being slightly more soluble than the nitrite and yet, when trying to separate a mixture of the two it looks like the nitrate is always the first to crystalize out .
Yes , I have been tested the crystals after every crystallization and most definitely the nitrate is crushing out while the concentration of the nitrite in the mother liquor is increasing after each crystallization.
I'm a bit confused. If anyone could help would much appreciate it .
 
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Solubilities listed are for solutions containing a single compound, not a mixture, plus these are very highly concentrated solutions, with very high ionic strengths, so it is quite unlikely they will follow simple "linear" models.

As a rule of thumb - if the amount of dissolved substance is comparable with the amount of solvent (as in: not orders of magnitude lower) things are almost guaranteed to go awry.
 
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Likes symbolipoint and Tas_T
Thanks for the reply.
So, could it be that if the compounds have similar solubility the one with higher concentration is likely to stay in solution ? I mean at least to a point ?
Gotta test that thought . . .
 
Tas_T said:
So, could it be that if the compounds have similar solubility the one with higher concentration is likely to stay in solution ? I mean at least to a point ?

"Likely" is too strong a word, more like "anything can happen" (definitely including the case where the higher solubility compound doesn't crash out first).
 
What I know and please correct me: a macroscopic probe of raw sugar you can buy from the store can be modeled to be an almost perfect cube of a size of 0.7 up to 1 mm. Let's assume it was really pure, nothing else but a conglomerate of H12C22O11 molecules stacked one over another in layers with van de Waals (?) "forces" keeping them together in a macroscopic state at a temperature of let's say 20 degrees Celsius. Then I use 100 such tiny pieces to throw them in 20 deg water. I stir the...

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