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Is it possible to regen Ferric Chloride at home?

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Steve H

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Feb 4, 2004, 1:31:14 PM2/4/04
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Hi,

I'm currently etching brass using Ferric Chloride solution purchased
from Radio Shack. Obviously after a while the reaction slows down and
I have to replenish the etchant.

Currently I am disposing the spent ferric chloride by first
neutralizing the acidity with baking soda and then flushing down the
toilet.

(Can anyone confirm if this is a good/bad/ugly disposal method?)

Anyway...

I have read many web pages that describe ways to regenerate the Ferric
Chloride using an oxidant - Hydrogen Peroxide has been mentioned more
than once. (Someone also suggested bubbling air through the solution
to slowly regenerate it)

Can anyone describe (quantatively) an "at home" way of regenerating
Ferric Chloride? I don't quite understand what happens to the
dissolved Copper salts - surely if they get converted back to Copper,
then the etching reaction will kick in again...?

I have about a 50% chemistry knowledge, so talk of anions, cations, et
al is OK, anything more and you might lose me...

Thanks,
Steve

Ron Jones

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Feb 4, 2004, 3:27:10 PM2/4/04
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You have converted copper(0) [the metal] into copper(II) ions (also called
cupric), by converting iron(III) ions (also called ferric) into iron(II)
ions (also called ferrous) - OK so far..?
By adding peroxide you will oxidize the iron(II) back to iron(III), and the
peroxide will turn into water.
Limiting problems. The peroxide you get is a solution, and therefore you
are adding water, this dilutes your concentration down, so you can't keep
regenerating (and anyway the copper salts will biuld up) - the other thing
to note is that by adding perioxide, you are not adding any counter ions
[the iron had 3 Cl, it drops to 2 Cl, and gives one to the copper - when you
add peroxide the iron would like 3 Cl again!] - you may need to add some
hydrochloric acid to redress the balance - or you will start getiing
precipitates of various hydroxides.

--
Ron Jones

Don't repeat history, see unreported near misses in chemical lab/plant
at http://www.crhf.org.uk


HLS

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Feb 4, 2004, 4:35:39 PM2/4/04
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You could probably work out a scheme to remove the copper ion by
electrolysis.Then touching up the remaining solution should not be too much
of a problem.

Cleaning up this sort of material would not be fincially attractive, were it
not for the environmental conscience of dumping heavy metal containing
solutions.


Muhammar

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Feb 4, 2004, 6:49:32 PM2/4/04
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FeCl3 acts as oxidant and goes to FeCl2. Copper gets oxidised into a
soluble form (CuCl2). It stays in the solution, so even after
"recycling" = re-oxidising iron in the spent etching bath back from
Fe(II) to Fe(III), the copper will remain dissolved.

As recycling the stuff means you have changing concentration of
components, the properties (and performance) of the etching bath can
change and that could give you poorly consistent results.

My suggestion is to not recycle.

If you want to save money, buy FeCl3.hydrate (or hexahydrate) or FeCl3
solution in a chemical supply store in bulk and dissolve/dilute it
down to the right concentration. You do not have to be exact when
preparing your own solution, kitchen or letter scale would be
sufficient for the purpose.

Also, it is not the acidity but metal content which is unpleasant
about the spent bath. Neutralising it does not prevent fishes from
getting your copper, because the formed carbonate sludge will
eventualy dissolve. You are not nice disposing it in this way. But
copper is not as bad as many other heavy metals, in Arizona water is
naturaly high in copper and water stone formed in sink in AZ can even
have a bluish tint because of Cu. So if you don't get caught, you are
not being completely evil. (But never pour mercury, thalium, cadmium
or lead down the drain).

kaste...@yahoo.com (Steve H) wrote in message news:<7a78d452.04020...@posting.google.com>...

Steve Turner

unread,
Feb 4, 2004, 7:25:19 PM2/4/04
to
kaste...@yahoo.com (Steve H) wrote:

>Hi,
>
>I'm currently etching brass using Ferric Chloride solution purchased
>from Radio Shack. Obviously after a while the reaction slows down and
>I have to replenish the etchant.
>
>Currently I am disposing the spent ferric chloride by first
>neutralizing the acidity with baking soda and then flushing down the
>toilet.
>
>(Can anyone confirm if this is a good/bad/ugly disposal method?)
>
>Anyway...
>
>I have read many web pages that describe ways to regenerate the Ferric
>Chloride using an oxidant - Hydrogen Peroxide has been mentioned more
>than once. (Someone also suggested bubbling air through the solution
>to slowly regenerate it)
>
>Can anyone describe (quantatively) an "at home" way of regenerating
>Ferric Chloride? I don't quite understand what happens to the
>dissolved Copper salts - surely if they get converted back to Copper,
>then the etching reaction will kick in again...?

We have been discussing this very topic recently: see the thread
"Making a small quantity of ferric chloride (III)".

You can drop out the copper by reducing it with iron:

Cu+2 + Fe ---> Fe+2 + Cu

This also reduces the remaining Fe+3 to Fe+2. So the second step is
to oxidize Fe+2 back to Fe+3:

2Fe+2 + Cl2 ---> 2Fe+3 + 2Cl-

Very neat.

Unfortunately, chlorine gas is not a good candidate for "home
chemistry." Perhaps you can use peroxide. I have not tried it.

Steve Turner

HLS

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Feb 7, 2004, 4:48:13 PM2/7/04
to

> Unfortunately, chlorine gas is not a good candidate for "home
> chemistry." Perhaps you can use peroxide. I have not tried it.
>
> Steve Turner


The whole project is an exercise in negative economics, but could be fun.
I think that he could build a small chlorine generator and operate it with
relative safety.
The hazards are there, but if one is adept at the art, it is possible to do.


Acid Test

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Feb 12, 2004, 4:33:52 PM2/12/04
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NaHCO3 + FeCl3 +(Cu+Ni+Zn)=

(CuCl+NiCl+ZnCl)+FeO + NaHCO2

The salts should be removed as well as the Ferric Oxide.

This can be achieved through a distillation process.

My guess is that the NaHCO2 can be seperated through distillation and
what is left is recrystallized metal salts and the ferric oxide.

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