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I have learned that sodium can be precipitated practically quantitatively as the mixed sodium-caesium hismuthinitrite (hexanitritobismuthate(III)) while potassium remains dissolved. hm...

@whitequark is it? *chuckles* I have a major fascination for these "wet" methods of analytical but they are somewhat outmoded professionally. As an amateur however I take an interest in low-tech methods of analysis.

@mona not even necessarily analysis, I can imagine wanting to selectively precipitate sodium. Or at least I definitely wanted that for something in high school... so long ago I no longer remember what for

@mona as an amateur I'm collaborating on building a QMS (sadly my great idea about significantly expanding m/z range and simplifying the drive circuitry at the same time didn't turn out to be so great) and otherwise would just subcontract to a commercial lab

@whitequark Mass spectroscopy is definitely an interest of mine but I have to put that one off into an indefinite future where I've finally amassed equipment to produce high vacuum. At the moment that's rather beyond me. It's occurred to me that I might be able to get pressures low enough with a simple titanium-wire pump.

@mona hmmm I may be able to send you a fully functional Edwards turbopump at a nominal cost

@whitequark I've had a very personal, strange fascination with chemical reagents that precipitate the alkali metals, all the weird little exceptions to the usual rules of solubility that everyone learns in high school or freshman classes: all sodium and potassium salts are soluble. The classical reagents for precipitating sodium were uranyl acetate, usually in conjunction with magnesium or zinc acetates; and potassium "pyroantimonate", really KSb(OH)6 I believe.

@whitequark but then I kept poking at the scientific literature over the years and found more. A peculiar and unstable acid formed from careful oxidation of tartaric acid, "diketosuccinic acid" or tetrahydroxysuccinic acid rather, is another good reagent for sodium. So is the O-methyl ester of mandelic acid and a few related organic acids. None of these is particularly accessible without a bit of work, but the bismuthinitrite reagent is quite simple in comparison.

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