[TheForge] coal or charcoal morph to Evaporust
Peter Fels & Phoebe Palmer
artgawk at thegrid.net
Thu Jun 26 00:30:49 EDT 2008
That is a neat trick Peter.
I'll play with it...thanks....pf
Peter Hirst wrote:
> Sounds like finishing hell to me, but I'm not all that adventurous. On
> the other hand, I did discover one neat trick that results in an
> interesting texturing. Put the workpiece on the negative clip for a day
> or two, and you get a huge, fast and unevenly distrubuted rust build
> up. Then reverse the polarity back to normal, popping the new rust off
> and you get texturing that raises pitting to an art form: more like
> cratering. But since the rust happens so fast, its not evenly
> distributed like it is if you leave a piece of iron where it can rust
> slowly and evenly. Instead, you get a deep rich texture which when
> cleaned up bright gives a real organic look, something you culd never do
> with a tool, and very different from the tell-tale pitting of the
> merely neglected or abused piece. I discovered this when I was setting
> up electrolysis on a piece that has been kicking around my shop for a
> couple of years and built up a nice even pitting from a couple of
> rust/wire wheel cycles. It just looked like a piece that had been
> rusted and brushed bright, so I decided to see what would happen if I
> exaggerated the effect by deliberately rusting it one more time. Pretty
> cool result.
> ----- Original Message ----- From: "Peter Fels & Phoebe Palmer"
> <artgawk at thegrid.net>
> To: "Blacksmithing List Sponsored by ABANA" <theforge at mailman.qth.net>
> Sent: Thursday, June 26, 2008 12:00 AM
> Subject: Re: [TheForge] coal or charcoal morph to Evaporust
>
>
>> Thanks Peter;
>> Sounds like finishing fun. Possibly using mixed metals,resists and
>> inclusions under a patina?
>> peter
>>
>> Peter Hirst wrote:
>>> He means FIRMLY as in electroplated. Whatever is in the anode that
>>> can be dissolved --chrome, copper from the battery clip, impurities
>>> etc -- will migrate through the solution and chemically bond with the
>>> work piece, but in an uncontrolled manner. SOme of these bonds are
>>> as strong as the crystalline structure of the iron itself. And some
>>> of these can actually promote re-rustingafter the treatment. This is
>>> one reason why an alkaline solution is recommended. No interference
>>> with the electrolytic reduction at the cathode (+).
>>>
>>>
>>> ----- Original Message ----- From: "Peter Fels & Phoebe Palmer"
>>> <artgawk at thegrid.net>
>>> To: "Blacksmithing List Sponsored by ABANA" <theforge at mailman.qth.net>
>>> Sent: Wednesday, June 25, 2008 10:23 PM
>>> Subject: Re: [TheForge] coal or charcoal morph to Evaporust
>>>
>>>
>>>> James;
>>>>
>>>> "you will end up
>>>> > with all kinds of junk firmly attached to your work piece."
>>>>
>>>> Please expand on this subject ,if the "firmly" part means permanent.
>>>> What is the final surface effect?.......pf
>>>>
>>>>
>>>>
>>>>
>>>> James Binnion wrote:
>>>>>
>>>>> On Jun 24, 2008, at 9:51 PM, Peter Hirst wrote:
>>>>>
>>>>>> Frosty: you answered your own question on the phosphoric acid.
>>>>>> Nasty stuff in any strength.
>>>>>
>>>>> It is used in many food products at the appropriate dilution (think
>>>>> soft drinks)
>>>>>
>>>>>
>>>>>> Not sure it would work in electrolyte bath. The electrolysis
>>>>>> tends to redeposit the iron back onto itself, while the phosphoric
>>>>>> acid tends to dissolve the elemental iron. The chemical action of
>>>>>> the acid and the electrlysis are two different reactions. The
>>>>>> sole function of the ion in the bath is to conduct electricity,
>>>>>> which in turn exactly reverses what happens in the the creation of
>>>>>> ferric oxide -oxidation. Phosphoric acid dissolves the iron
>>>>>> itself, which is why its used to etch for other fininsh preps.
>>>>>
>>>>> The rust dissolving nature of your electrolytic setup is from the
>>>>> reduction of the iron oxide (rust) back to iron by the atomic
>>>>> hydrogen liberated at the cathode(-) from the electrolysis of the
>>>>> water in your electrolyte. If you use an acid like phosphoric in
>>>>> the electrolyte solution you will end up dissolving the anode(-)
>>>>> into the electrolyte and those ions will then plate out on the
>>>>> workpiece which you really don't want them to do. This is the basis
>>>>> for electroplating but your electrolyte will not be a very good
>>>>> plating solution and you will end up with all kinds of junk firmly
>>>>> attached to your work piece.
>>>>>
>>>>> James Binnion
>>>>> jbin at well.com
>>>>>
>>>>>
>>>>>
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