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Author: Subject: How to reduce HgCl back to metal?
thrival
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[*] posted on 14-2-2015 at 08:12
How to reduce HgCl back to metal?


Is there a simple, fast and/or efficient way to do this? I read the metals all do this but forming amalgams isn't useful to me, I want my liquid quicksilver back!
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blogfast25
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[*] posted on 14-2-2015 at 08:46


You mean HgCl<sub>2</sub>, right? Mercuric chloride.

Mercuric ions are easy to reduce:

Hg<sup>2+</sup>(aq) + 2 e- -----> 2 Hg(l) has a reduction potential of +0.85 V

(http://chemprof.tripod.com/redtable.htm)

Anything with a lower reduction potential is thus in principle capable of reducing the mercuric ions to mercury metal. Copper for instance would do it.

So make solution of mercuric chloride and choose a reducing metal, preferably one that doesn't amalgamate with mercury easily.

Gentle electrolysis of an aqueous mercuric chloride solution with carbon electrodes should also work well.

Mind the high toxicity of all things mercurial!

[Edited on 14-2-2015 by blogfast25]




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Boffis
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[*] posted on 14-2-2015 at 10:33


Which mercury chloride is it though? Do you have:

Hg2Cl2 - mercurous chloride - the insoluble type
HgCl2 - mercuric chloride - the soluble type

Both chlorides are decomposed by a large excess of alkali hydroxide. When a suspension of mercurous chloride is treated with excess hot alkali hydroxide it is converted to a black mixture of mercury and mercuric oxide. Without isolation the mercuric oxide can be reduced by almost any reducing agent but hydrazine or hydroxylamine are usually used because they are clean (oxidation products N2 and H2O).

I suspect therefore that mercuric chloride with be similarly converted to mercuric oxide by excess alkali and can then be reduced to mercury as above. Mercuric chloride is a curious compound because it is almost undissociated and while the nitrate and sulphate immediate deposit yellow mercuric oxide the chloride may not. In neutral and acid conditions almost all reducing agents precipitate the mercurous chloride apart from a few sulphur bearing compounds (ie thiosulphates) when the reaction is complex and the precipitate is discoloured by sulphur containing compounds.

Avoid ammonia because it converts both valencies of Hg into hellish intractable aminomercury compounds. I suggest you read up on some mercury chemistry though before you try this reduction. There are a couple of comprehensive textbooks on the SM website library.

These things said I think your best route is via reduction in alkali hydroxide to avoid the formation of mercurous compounds.
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SimpleChemist-238
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[*] posted on 20-2-2015 at 11:20


Here is a good chart!




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[*] posted on 21-2-2015 at 16:58


Be VERY careful with mercury compounds. Mercury accumulates in your body, increasing the chance of cancer and brain damage.
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MrHomeScientist
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[*] posted on 23-2-2015 at 07:53


SimpleChemist, I have that very chart posted on my wall right now! Very handy reference.

Iron flasks are traditionally used for mercury storage and transport, because the metals do not form an amalgam. My dad used to tell stories of how he would rub mercury onto pennies to give them a silvery shine - from that I conclude that copper would not be the best choice for reduction. If that isn't strictly amalgamation, it at least sticks to copper and would be difficult to remove. Perhaps an iron bar dropped in a solution of HgCl<sub>2</sub> (assuming that's what you have) would do the trick. Be sure to come up with a safety & waste disposal plan before conducting any experiments with soluble mercury compounds!
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