Maybe a safer method for ball-milling metals?
#1
Posted 06 August 2008 - 03:53 PM
I have some magnesium turnings, from which I wish to obtain magnesium in a powdered form.
I am aware of the dangers involved in ball-milling metals, notably pyrophoricity (many metals have the potential for undergoing spontaneous combustion when exposed to atmospheric oxygen in finely divided form).
Would it be safer to ball-mill my magnesium with the inclusion of an oil (such as linseed oil) to pervent the exposure to atmospheric oxygen?
What are your thoughts on this?
Could the same be done with other metals, such as aluminium or titanium?
I could use acetone to wash-off the oil after milling is complete, but first I need to find out whether finely powdered Mg is reactive with acetone (like it is with water or alcohol).
In the eventuality of a fire, there should be no real danger, since I do my ball-milling in my spacious garden, well away from the house.
#2
Posted 07 August 2008 - 02:27 PM
Yes, I have searched the forum!
Edited by Gary, 07 August 2008 - 02:30 PM.
#3
Posted 07 August 2008 - 02:42 PM
#4
Posted 07 August 2008 - 03:00 PM
First of all the oil would have 2 unwanted side affect, it would drastically increase the milling time for 2 reasons reduce friction but more importantly it would act like a heat sink drawing away heat from the metal and drastically increasing the time required to impact harden the metal, depending on the amount of oil, it might even making impact hardening impossible.
But more importantly it will not necessarily prevent pyroforic reaction from taking place, it will only dalay it and possibly cause it to happen in a less violent and in a more controlled manner.
I personally think filling your tube with Argon/Helium/Pure Nitrogen is a much safer alternative and it allows you to include boric acid during the ball milling process; the boric acid will protect the surface of the aluminum while it won't entirely eliminate the danger it will reduce the risk significantly of the metal reacting once exposed to air.
Might I add that before opening the tube, the tube should be allowed to rest for several hours to allow the heat built up during milling to dissipate and to and the airborne aluminium to settle in the bottom.
but a much faster and more efficient way of making you alunium is in a hammer mill... but since most of us don't have one of those and we all have ball mill, it's worth trying.
#5
Posted 07 August 2008 - 03:55 PM
I once processed some Mg turnings that I got from drilling a piece of Mg. I put them in the coffee grinder for a few seconds, and then ball milled. I stopped the mill maybe every hr or so, let it sit for a few minutes and then opened to air it out, before continuing to mill (I also do this with MgAl).
The end product with the Mg was -100 mesh, in a sort of flake/needle form. With the MgAl I can easily mill to pass 250 mesh which is the finest screen I have.
Mg should be fine to wash with DRIED acetone (not sure exactly how to dry it, but the info is out there somewhere). the Mg can then be coated with linseed oil or potassium dichromate.
@bigtonyicu: I don't really understand any reason to add boric acid to the mill when processing Al to act as a coating, I would think of adding stearic acid/strearine if anything... And with using a gas isn't the risk usually when the jar is opened? If that's the case i don't see how the gas would really help as the jar must be opened at some point.
#6
Posted 07 August 2008 - 05:23 PM
#7
Posted 07 August 2008 - 07:02 PM
I tried milling pure Mg and found it quite difficult, it's a relatively soft metal and seems to just deform rather than breaking up. MgAl is much easier to powder.
When I milled the Mg I don't remember how long the mill ran (about 2 years ago) but I think it easily totalled several full days.
#8
Posted 08 August 2008 - 04:49 PM
#9
Posted 08 August 2008 - 05:21 PM
Many thanks for your suggestions. I think I'll try using an inert gas (helium springs to mind) to provide my magnesium with an oxygen-deficient atmosphere whilst milling.
It may prevent an issue while milling, but keep in mind the Mg WILL be exposed to air when the jar is opened...be careful.
Also, I would go with Argon over helium, it is cheaper for one and is also heavier than air, therefore it will displace the air as you blow it into the jar.
Edited by Bonny, 08 August 2008 - 05:26 PM.
#10
Posted 09 August 2008 - 07:32 AM
#11
Posted 09 August 2008 - 08:45 AM
Butane is another option.
Correct me if im wrong, but isn't butane flammable ? If he is trying to avoid a pyroforic reaction, then butane isn't a good option, a small spark could ignite it.
If It Aint Broke, Then Why The Hell Are You Trying To Fix It!!!
#12
Posted 09 August 2008 - 09:24 AM
#13
Posted 09 August 2008 - 09:35 AM
#14
Posted 09 August 2008 - 09:39 AM
Hi,.................
In the eventuality of a fire, there should be no real danger, since I do my ball-milling in my spacious garden, well away from the house.
Down the garden is just where the neighbours will see everything if there is a fire! You do not usually miss a magnesium fire - think bright then multiply by100!
Property damage is undesireable but upsetting the neighbours could cause you much more harm and local ill feeling.
Can you not buy magnesium powdered to the size and style that you want? Magnesium from a chemical supply house should have a specific analysis, magnesium found as supposedly magnesium castings at a scrap yard will have no known analysis.
Keep mannequins and watermelons away from fireworks..they always get hurt..
#15
Posted 09 August 2008 - 12:35 PM
The reaction is basically the oxidisation of exposed metal surfaces and as the metal is ground smaller and smaller the surface area goes up in comparison, this increase is I believe exponential in that the surface area increases much faster the smaller the particles get. 100# particles don't have 10 x the surface area of 10# particles but many many times more and 400# has many hundreds (maybe many thousands) times more than the 100#
I personally believe milling with an amount of linseed oil may cure the pyroforic reaction as it will be evenly distributed on the particles and will create a protective layer when exposed to the atmosphere. This will basically do the same as we already use it for on iron filings and magnesium.
If not then opening the jar regulally will allow air and therefore oxygen into the jar and allow the surface of the freshly milled metal to oxidise slowly and in a controlled manner preventing or at least reducing the chances of an accidental ignition which would only occour when opening the jar with the rush of air entering the now oxygen starved mill jar (oxygen starved due to the reaction inside the jar with what oxygen was available but not replaced)
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