Sciencemadness Discussion Board

Nickel, Iron, and Molybdenum from Mu-Metal (Hard Drives)

VSEPR_VOID - 27-5-2018 at 19:16

After conducting a search of the forum and wiki for information regarding the purification of primarily nickel from Mu-metal alloysSource 1, I found that there were no procedures that have been written. Having 154.7 grams of this alloy myself, I would like to try my hand at this.

For anyone with a few hard drives sitting around they are an excellent source interesting metals. Potentially just from these pieces of metal a nickel, iron, and molybdenum can be extracted. Aside from that, the magnets contain neodymium (my next project), the platters contain small amounts of platinum, and so on.

Mu-metal contains between 77-80% nickel, 12-16% iron, 0-5% copper, 0-2% chromium,0-5% molybdenum, and trace amounts of silicon. Source 1 It is contained within modern hard drives as a shielding around neodymium magnets (about 50 grams/hard drive).

Here are my thoughts so far;

Considering that both nickel and iron metal are both magnetic at room temperature, they may be separated from the non-ferromagnetic metals like chromium and copper.

The whole alloy can be dissolved using HCl and H2O2, leaving behind the silicon.

Iron and nickel have very similar properties and will be difficult to separate from one another.

With what acids will nickel and iron not react and react? Sources online have not been specific.


Source 1: http://www.sciencemadness.org/smwiki/index.php/Mu-metal

USC10K900.jpg - 191kB download.jpg - 15kB

[Edited on 28-5-2018 by VSEPR_VOID]

j_sum1 - 27-5-2018 at 19:27

Magnetic separation ain't going to help you separate elements of an alloy. Your choices are going to be either some kind of wet chemistry approach or selective oxidation at high temperatures (which is what is done to refine steels.)

I think you need to as a first step dissolve in a strong acid. Then you can selectively precipitate out the species you are after.
I am doing a similar experiment extracting vanadium from a pile of rusted screwdriver bits. I used HCl because that is what I have on hand. I have not yet decided on a procedure for separating the vanadium from the iron: I need to do some more reading.

There are procedures out there for separating chromium and nickel from iron -- look up the dichromates from stainless steel threads. The interesting target I think is the molybdenum. Good luck!

VSEPR_VOID - 27-5-2018 at 19:38

Quote: Originally posted by j_sum1  
Magnetic separation ain't going to help you separate elements of an alloy. Your choices are going to be either some kind of wet chemistry approach or selective oxidation at high temperatures (which is what is done to refine steels.)


I was not clear when I mentioned separation based on ferromagnetic, or lack-there-of, properties, I meant the precipitation of metals from solution (created by dissolving the metal in acid) using aluminium, and removing the nickel and iron metal using a magnet. This would leave with nickel and iron metal.

It might be possible to allow the iron to oxidize, perhaps by using a solution of salt water, then again use a magnet to removed the nickel.


I too agree that Mo seems like a interesting target. I unfortunately know nothing about its chemistry. Could you recommend a text on the topic?

ninhydric1 - 27-5-2018 at 20:08

Nickel forms a complex with ammonia, iron doesn't. You can use that to separate the two ions. Copper(II) ions can be reduced to insoluble copper(I) salts using iodide ions, ascorbic acid, etc.

Using a ferromagnetic approach sometimes doesn't work, as the metal powder that precipitates is sometimes a mix of atoms interlocked in a crystal lattice.

RogueRose - 27-5-2018 at 20:21

I have a lot of these metal plates and have thought about doing this before and stopped because it looked like A LOT of work with the potential of small returns and creating a lot of toxic waste. The chromates thread is a good start but also separating the Ni and Cu is going to be a PITA as well.

I looked into separating the neodynium from the mags as the recovery rate was extremely low (about 1-2% yield) in many cases so I decided against the whole experiment.

Is this just to practice separation or to obtain usable reagents?

[Edited on 5-28-2018 by RogueRose]

j_sum1 - 27-5-2018 at 20:21

My Mo chemistry is limited to a short experiment dissolving Mo wire in various acids with and without peroxide. I forget the results but I can look them up. Oh, and I have also used Mo compounds in testing for phosphates.

I am sure that there are good texts you could use though.

VSEPR_VOID - 27-5-2018 at 21:13

Quote: Originally posted by ninhydric1  
Nickel forms a complex with ammonia, iron doesn't. You can use that to separate the two ions. Copper(II) ions can be reduced to insoluble copper(I) salts using iodide ions, ascorbic acid, etc.

Using a ferromagnetic approach sometimes doesn't work, as the metal powder that precipitates is sometimes a mix of atoms interlocked in a crystal lattice.


Is the complex insoluble? I have seen photographs of a nickle complex of ammonia but there is no precipitate present.

The copper reduction is a good idea, do you have a procedure that you know works? Would that also reduce iron?

That fact about interlocking atoms in crystal lattices is interesting.

Quote: Originally posted by RogueRose  

I have a lot of these metal plates and have thought about doing this before and stopped because it looked like A LOT of work with the potential of small returns and creating a lot of toxic waste. The chromates thread is a good start but also separating the Ni and Cu is going to be a PITA as well.

I looked into separating the neodynium from the mags as the recovery rate was extremely low (about 1-2% yield) in many cases so I decided against the whole experiment.

Is this just to practice separation or to obtain usable reagents?


You should try it. Considering the alloy is mostly nickel it is not a bad source of the metal. It also might be economic considering that nickel nitrate is 12 dollars for about 60 grams online. 100g is about 10 dollars on ebay (not considering bulk orders of 1 pound which are 30 dollars).

My goal is to extract a pure Ni salt, Fe salt, and Mo salt for use in making ferrocyanides. I am hoping for a yield of between 80 and 100g of nickel metal equivalent.




My experimentation so far


23.4g of Mu-metal was added to a 600ml beaker. To it 150 ml of 31.45% HCl and 100ml of 3% hydrogen peroxide. The solution was gently heated to 80C with some stirring. There evolved a large amount of gas and the solution turned urine yellow. This color is probably due to iron (III) chloride in solution.

[Edited on 28-5-2018 by VSEPR_VOID]

20180528_003503.jpg - 520kB

wg48 - 27-5-2018 at 22:13

Vsepr-void:

I will be very surprised if you have more than a trace of nickel in that solution and what is there may be from the nickel-plating the bracket has.

The brackets pointed to in the first post are part of the magnetic circuit of the neo magnets and are usually made from soft iron (almost pure iron). They hold the magnets in place and conduct the magnetic flux between the rear faces (the opposite face to the ones next to the coil). Soft iron is used as it has a high permeability and high saturation. Mu metal would saturate.


VSEPR_VOID - 27-5-2018 at 23:55

Quote: Originally posted by wg48  
Vsepr-void:

I will be very surprised if you have more than a trace of nickel in that solution and what is there may be from the nickel-plating the bracket has.

The brackets pointed to in the first post are part of the magnetic circuit of the neo magnets and are usually made from soft iron (almost pure iron). They hold the magnets in place and conduct the magnetic flux between the rear faces (the opposite face to the ones next to the coil). Soft iron is used as it has a high permeability and high saturation. Mu metal would saturate.



Than why is it stated on the wiki that the brackets are 77% Ni metal?
http://www.sciencemadness.org/smwiki/index.php/Mu-metal

Update on the reaction: The solution is still yellow and the mu-metal's coating as not dissolved but the insides nearly have completely. Almost like a penny placed in hydrochloric acid, dissolving the zinc but not the copper.

unionised - 28-5-2018 at 01:30

Quote: Originally posted by VSEPR_VOID  




Than why is it stated on the wiki that the brackets are 77% Ni metal?
http://www.sciencemadness.org/smwiki/index.php/Mu-metal


Possibly because it was written by someone who was mistaken.

You have a solution that contains some of the metal.
If you add excess ammonia then the iron will fall out as a mixture of hydroxides/ oxides etc and nickel will remain in solution as a purplish blue complex (much the same colour as the copper ammine complex).
So you can do that test now and settle the matter.

VSEPR_VOID - 28-5-2018 at 01:33

That is very disappointing. Someone should change the wiki at once! The solution is only yellow. If it is just iron it may not be worth doing anything with it.

wg48 - 28-5-2018 at 01:37

Quote: Originally posted by VSEPR_VOID  
Quote: Originally posted by wg48  
Vsepr-void:

I will be very surprised if you have more than a trace of nickel in that solution and what is there may be from the nickel-plating the bracket has.

The brackets pointed to in the first post are part of the magnetic circuit of the neo magnets and are usually made from soft iron (almost pure iron). They hold the magnets in place and conduct the magnetic flux between the rear faces (the opposite face to the ones next to the coil). Soft iron is used as it has a high permeability and high saturation. Mu metal would saturate.



Than why is it stated on the wiki that the brackets are 77% Ni metal?
http://www.sciencemadness.org/smwiki/index.php/Mu-metal

Update on the reaction: The solution is still yellow and the mu-metal's coating as not dissolved but the insides nearly have completely. Almost like a penny placed in hydrochloric acid, dissolving the zinc but not the copper.


I have given you my reasoning why I think its not Mu metal, I suggest you ask the author of the wiki why he thinks it is Mu metal. No real reference was given.

Perhaps the plating on the bracket (possibly electro less nickel/phosphorous alloy) did not dissolve and the inner iron is dissolving.

When I have used HCl to dissolve parts of a magnetron. I got impatient and added H2O2 then heated the solution. That was a bad idea it gave off a lot chlorine and the heat probably decomposed any H2O2 that was left. It probably would have been better (used less acid and peroxide) to not have heated the solution. Perhaps that’s why your plating did not dissolve.

I thought nickel chloride was green even in HCl. Of cause you will soon be able to definitively say if there was significant nickel in your bracket.

I just checked the colour of a few crystals of nickel chloride in HCl and it is green.

[Edited on 28-5-2018 by wg48]

VSEPR_VOID - 28-5-2018 at 02:13

Yes, its strange that that the solution is still yellow. It shows no colors of nickel or cobalt. I think you might be right, in which case I am deeply disappointed.

unionised - 28-5-2018 at 03:33

Quote: Originally posted by VSEPR_VOID  
That is very disappointing. Someone should change the wiki at once! The solution is only yellow. If it is just iron it may not be worth doing anything with it.


It is worth adding excess ammonia solution to a little of the solution in order, once and for all, to find out if the stuff you have made has nickel in it

Foeskes - 28-5-2018 at 06:57

The last time I tried to separate Ni from Fe using ammonia failed horribly.
It did nothing but make the area pungent.
For some reason little to no nickel dissolved.

ninhydric1 - 28-5-2018 at 10:55

I have no idea what you're referring to. VSEPR here is trying to extract some potentially useful and exotic metals from a metal alloy, and none of what you have said will give him more information about his current experiment. [Edit by j_sum1 -- Refers to troll posts later pruned from thread]

Back to the topic, it might be just iron. Besides Canadian nickels, there are rarely any commonly available alloys with even 50+% nickel in them.

Reducing iron(III) to iron(II) won't form a precipitate because both are soluble in water. Copper(I) salts are not soluble in water regardless, which makes the reduction method for separating out copper work.

I have tried this using colorless iodine tincture (no free I2 in solution) and it does separate out copper as copper(I) iodide to some extent, but I happened to run out of the tincture and had to put it off for another day.


[Edited on 28-5-2018 by j_sum1]

VSEPR_VOID - 28-5-2018 at 14:20

An Update On Reaction Progress: The solution has turned a darker yellow and the case has no dissolved, only the inner metal. I hypothesize that that case is made of something like cobalt and the insides steel or iron.

The case is resistant to HNO3, and HCl with H2O2 and heating.

Does anyone know a way to test the yellow solution for other metal ions to determine if it is steel or some other alloy?

ninhydric1 - 28-5-2018 at 14:52

IIRC woelen mentioned something about adding H2O2 to determine the presence of chromium. If there is chromium present, it should turn into a violet-blue color.


http://www.sciencemadness.org/talk/

VSEPR_VOID - 28-5-2018 at 15:39

I will try that. I am hoping at this point I can at least get some nice ferric chloride out of this. The casing might be cobalt so that might be the best new target for this project.

Edit: After doing more research I found that the original claim on the SM wiki that the articulator's NdFeB bracket (it should be noted that the actual magnet is coated in nickel) is composed of Mu-metal originated from an non-cited claim on Wikipedia.

An hour in the library will save you 3 in the lab.

I still have another 130g of these brackets. If I can discover the composition of the acid resistant coating, and of the solution produced by dissolving the internal metal in HCl, then the project may still be salvaged.

Potentially from this I may be able to salvage 80-120g of iron (relative to the salt) and also what ever metal is coating them.

Additionally there are also the magnets to consider. I plan on taking this up next. If you are going to take apart of hard drive to get the magnets, you might as well also find a use for the other parts.

[Edited on 29-5-2018 by VSEPR_VOID]

unionised - 29-5-2018 at 01:59

Quote: Originally posted by VSEPR_VOID  

I still have another 130g of these brackets. If I can discover the composition of the acid resistant coating,

[Edited on 29-5-2018 by VSEPR_VOID]

Nickel is remarkably resistant to acids. I have a coin sitting in sulphuric acid % which as been "dissolving" for months. It's still there, you can read the embossed lettering.

Nickel is also a very plausible coating for the brackets.

VSEPR_VOID - 29-5-2018 at 02:03

Quote: Originally posted by unionised  
Quote: Originally posted by VSEPR_VOID  

I still have another 130g of these brackets. If I can discover the composition of the acid resistant coating,

[Edited on 29-5-2018 by VSEPR_VOID]

Nickel is remarkably resistant to acids. I have a coin sitting in sulphuric acid % which as been "dissolving" for months. It's still there, you can read the embossed lettering.

Nickel is also a very plausible coating for the brackets.


Have you tried dissolving it in another acid. At this point I am considering either boiling strong NaOH solution or aqua regia.

unionised - 29-5-2018 at 02:06

Quote: Originally posted by VSEPR_VOID  

I still have another 130g of these brackets. If I can discover the composition of the acid resistant coating,

[Edited on 29-5-2018 by VSEPR_VOID]

Nickel is remarkably resistant to acids. I have a coin sitting in sulphuric acid % which as been "dissolving" for months. It's still there, you can read the embossed lettering.

Nickel is also a very plausible coating for the brackets.

VSEPR_VOID - 29-5-2018 at 03:48

Quote: Originally posted by unionised  
Quote: Originally posted by VSEPR_VOID  

I still have another 130g of these brackets. If I can discover the composition of the acid resistant coating,

[Edited on 29-5-2018 by VSEPR_VOID]

Nickel is remarkably resistant to acids. I have a coin sitting in sulphuric acid % which as been "dissolving" for months. It's still there, you can read the embossed lettering.

Nickel is also a very plausible coating for the brackets.


I am considering trying either hot concentrated sodium hydroxide or aqua regia.

Mabus - 29-5-2018 at 06:43

As the guy who wrote the Mumetal page on the wiki, I feel the need to clarify than all the specs I've encountered about hard drives, say that the magnet brackets are Mumetal, and that mumetal is specified to be a nickel alloy. I too have several magnet brackets from various different types of hard drives, but unlike some people here, I haven't had any success dissolving anything: HCl gave me no reaction, adding a bit of 3% hydrogen peroxide gave me just a little rust, which, given that the alloy has iron, it should be expected, but other than than slight coloring of the solution, not much has happened. Sulfuric acid 30% didn't do anything. The only more corrosive stuff that I haven't tried are halogens, such as iodine or chlorine (as bleach).
There is another possibility as to why you didn't get the nickel coloring: your "Mu-metal" from the brackets is not true mu-metal. Years ago, when I took apart lots of hard drives, I found an old hard drive that had galvanized brackets and what I think it was a samarium-based magnet (well, some old but strong magnets). I found it odd why it won't be nickle plated like the rest of the hard drive magnet brackets, so I added a bit of acid, but not much happened. The next day the bracket was covered in rust in the area where I added the acid, which led me to believe that it probably wasn't a nickel alloy, but rather some iron alloy with high magnetic permeability, probably because it was cheaper, or because nickel alloys were more expensive back then.
Another possibility is that it is a nickel alloy, but for some reason only the iron dissolves. It's not the first time I've encountered nickel alloys that "rust". A few years ago I scavenged some heating elements that were very rusty, but when I placed them in HCl acid, the only thing that happened is that the rust was removed, while the metal wire did not dissolve, even after a few days of sitting in acid. Well, I assume the wire was nickel alloy, since if it was chromium alloy, some of it should have dissolved.

fusso - 29-5-2018 at 09:04

If Ni in mumetal didn't dissolve in acids then why Ni in stainless steel do dissolve?
I tried dissolving SS in HCl previously and all Ni dissolved.

wg48 - 29-5-2018 at 11:48

Quote: Originally posted by Mabus  
As the guy who wrote the Mumetal page on the wiki, I feel the need to clarify than all the specs I've encountered about hard drives, say that the magnet brackets are Mumetal,
snip


Correct or not thanks for your work on the wiki Mabus.

Do you have a link to or a copy of one of those spec?

I have several magnets I extracted from defunct hard drives but I did not save the brackets. If you still have a bracket you could try cutting or breaking one up to expose the core material and then attempt to dissolve it in HCl. I assume soft iron will dissolve easily.


I tried googling for material info on those brackets but did not find any primary reference. One utuber after noticing his screwdriver was more strongly attracted to the magnet face than the opposite side on the bracket concluded the bracket was a magnetic shield and therefore was Mu metal an erroneous conclusion. Any steel, soft iron or sufficiently magnetic material would have the same effect. Closing the loop round the magnets not only increases their strength it also reduces stray fields. Mu metal shields would be placed as an outer shield specifically not in direct connection or in the main flux path of the magnets to avoid magnetic saturation of the mu metal which would reduce its screening.

Of cause this does not preclude the material of the bracket being some other magnetic alloy compatable with the flux level of the neo magnets though I doubt that they are.

VSEPR_VOID - 29-5-2018 at 12:04

Quote: Originally posted by Mabus  
As the guy who wrote the Mumetal page on the wiki, I feel the need to clarify than all the specs I've encountered about hard drives, say that the magnet brackets are Mumetal, and that mumetal is specified to be a nickel alloy. I too have several magnet brackets from various different types of hard drives, but unlike some people here, I haven't had any success dissolving anything: HCl gave me no reaction, adding a bit of 3% hydrogen peroxide gave me just a little rust, which, given that the alloy has iron, it should be expected, but other than than slight coloring of the solution, not much has happened. Sulfuric acid 30% didn't do anything. The only more corrosive stuff that I haven't tried are halogens, such as iodine or chlorine (as bleach).
There is another possibility as to why you didn't get the nickel coloring: your "Mu-metal" from the brackets is not true mu-metal. Years ago, when I took apart lots of hard drives, I found an old hard drive that had galvanized brackets and what I think it was a samarium-based magnet (well, some old but strong magnets). I found it odd why it won't be nickle plated like the rest of the hard drive magnet brackets, so I added a bit of acid, but not much happened. The next day the bracket was covered in rust in the area where I added the acid, which led me to believe that it probably wasn't a nickel alloy, but rather some iron alloy with high magnetic permeability, probably because it was cheaper, or because nickel alloys were more expensive back then.
Another possibility is that it is a nickel alloy, but for some reason only the iron dissolves. It's not the first time I've encountered nickel alloys that "rust". A few years ago I scavenged some heating elements that were very rusty, but when I placed them in HCl acid, the only thing that happened is that the rust was removed, while the metal wire did not dissolve, even after a few days of sitting in acid. Well, I assume the wire was nickel alloy, since if it was chromium alloy, some of it should have dissolved.


I believe the reason that I have a reaction from HCl/H2O2 and you did not was because my bracket was scratched in several places, letting the acid get to the iron inside.

battoussai114 - 29-5-2018 at 19:19

Have you, Vsper or Mabus, tried and oxidizing acid like nitric? might be worth a shot dissolving the possible mumetal coat.


Quote: Originally posted by fusso  
If Ni in mumetal didn't dissolve in acids then why Ni in stainless steel do dissolve?
I tried dissolving SS in HCl previously and all Ni dissolved.

Generally Nickel and it's alloys don't handle HCl or chlorides particularly well. But alloys are complicated and maybe there's some intergranular attack happening at an iron rich boundary of a nickel rich intermetallic that's resistant to the acid attack, I'd expect this to result in something similar to the selective leaching we see in dezincification of brass.

(Just speculating here though)

VSEPR_VOID - 29-5-2018 at 23:52

Here is what the solution looks like now. The picture was taken during light heating.

The solution is now much more green rather yellow. This is probably ferrous chloride (+3). The skin of the bracket is slightly tarnished now.

I am hoping that the coating will not dissolve, allowing me to experiment with it.

20180530_033247.jpg - 671kB

VSEPR_VOID - 31-5-2018 at 00:12

Everything has dissolved, coating and all. The solution looks like very strong ferric chloride.

Are there any tests I could use for determining chromium, nickel, or copper content. I have a visible light spec I could use so that could tell me a lot. I could look for absorbance peeks for copper and nickel chloride. Are there any databases with that data?

Texium - 31-5-2018 at 09:43

Add concentrated ammonia to it until it is highly basic, then filter out any precipitate formed. Nickel and copper should be left in solution as their amine complexes while iron precipitates. If the solution is blue/purple, that's already a good indicator of a significant amount of nickel being present. You should be able to look up the maximum absorbance values for these coordination complexes, and therefore be able to use your spec and a quick Beer's law calculation to determine the concentration.

walruslover69 - 31-5-2018 at 10:04

Another potential method could be to use acetone. I found that both iron chlorides are very soluble in acetone. So i would recommend boiling down your solution and precipitating your NiCl2 with acetone which is negligibly soluble.

VSEPR_VOID - 31-5-2018 at 18:58

I can not find any data on the solubility of nickel chloride in acetone.

walruslover69 - 31-5-2018 at 19:41

I could only find this one source
https://books.google.com/books?id=7L0MAAAAYAAJ&pg=PA537&...

I also found ferric chloride to be 10 times more soluble that nickel chloride in ethanol.
http://periodic-table-of-elements.org/SOLUBILITY/ferric-III_...
http://periodic-table-of-elements.org/SOLUBILITY/nickel-II_c...

Upon further look I believe those numbers are only for the anhydrous salts and so precipitating out might not work very well, but evaporating the water and baking the salts to dehydrate them and then redissolving the iron in acetone or water would probably work.

VSEPR_VOID - 1-6-2018 at 03:18

Quote: Originally posted by walruslover69  
I could only find this one source
https://books.google.com/books?id=7L0MAAAAYAAJ&pg=PA537&...

I also found ferric chloride to be 10 times more soluble that nickel chloride in ethanol.
http://periodic-table-of-elements.org/SOLUBILITY/ferric-III_...
http://periodic-table-of-elements.org/SOLUBILITY/nickel-II_c...

Upon further look I believe those numbers are only for the anhydrous salts and so precipitating out might not work very well, but evaporating the water and baking the salts to dehydrate them and then redissolving the iron in acetone or water would probably work.


I have a liter of dry ethyl alcohol I received for free as a sample. I could use that after roasting the solution's solutes in a steel can (to prevent breaking or damaging a beaker).

Ferric Chloride decomposes at 280C to the anhydrous salt and I will have to take care not to heat it above 316. This presents a difficulty as I have no way to measure that temperature. Anhydrous nickel chloride does would be safe to roast on a hotplate without fear of decomposition.


What other sources of nickel metal are there? Any pure?


[Edited on 1-6-2018 by VSEPR_VOID]

walruslover69 - 1-6-2018 at 09:16

I don't see a reason why you would want/need to oxidize to ferric chloride in the first place. Ferrous chloride has similar solubility in ethanol (100g/100ml).
https://onlinelibrary.wiley.com/doi/10.1002/047084289X.ri055

Both nickel and ferrous chloride are heat stable up to like 500+ degrees so you shouldn't have a problem drying them that way. Alternatively you could dry them through azeotropic distillation with toluene but that sounds like a lot of work.

I don't know of any OTC sources of pure nickel. If you live here in the U.S then 5 cent nickel coins could be a promising source. They are 25% nickel and 75% copper. I would estimate that there would be minimum impurities, since the Mint keeps relatively high standards. I have actually been considering doing this for a long time but I have been hesitant to waste some of my nitric acid on it.

wg48 - 1-6-2018 at 09:54

Quote: Originally posted by VSEPR_VOID  



I have a liter of dry ethyl alcohol I received for free as a sample. I could use that after roasting the solution's solutes in a steel can (to prevent breaking or damaging a beaker).


Perhaps you will discover a way to get the nickel out if you put the solution in a steel can. I think iron will displace nickel from its chloride solution and therefore will plate out on to the steel can. Ok that does not help separate the nickel from the iron in the can if its adherent but you will know if nickel is in the solution. You will need the can surface to be clean and not tinned and/or not coated.

VSEPR_VOID - 1-6-2018 at 11:47

Quote: Originally posted by wg48  
Quote: Originally posted by VSEPR_VOID  



I have a liter of dry ethyl alcohol I received for free as a sample. I could use that after roasting the solution's solutes in a steel can (to prevent breaking or damaging a beaker).


Perhaps you will discover a way to get the nickel out if you put the solution in a steel can. I think iron will displace nickel from its chloride solution and therefore will plate out on to the steel can. Ok that does not help separate the nickel from the iron in the can if its adherent but you will know if nickel is in the solution. You will need the can surface to be clean and not tinned and/or not coated.


I think that would work as long as I can remove the zinc coating. Alternatively I could just find some iron nails or wool.



[Edited on 1-6-2018 by VSEPR_VOID]

[Edited on 1-6-2018 by VSEPR_VOID]

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VSEPR_VOID - 1-6-2018 at 21:32

Update:

The brackets are just clearly an alloy of iron with a coating of nickel. The solution resulting from dissolving them in HCl-H2O2 is not worth separating.

That being said I did go ahead and boil the solution as I said I would do in a steal can. The solution became bright green and the surface of the can became eroded and and dull in color. The resulting solution was filtered and boil down by 30%. Upon cooling a film of white crystals formed. The green is probably from ferrous chloride after the ferric chloride was reduced by the steel during boiling. Nickel metal must have precipitated out and been replaced with iron/zinc in solution.

Nickel can be separated alternatively from US nickels so going out and finding hard drive brackets is not worth it.

Important Proceedings

After completely boiling down the solution I was left with fluffy green crystals pictured bellow. I proceeded to take a gram of this material and place it in a test tube with water, then added strong sodium hydroxide solution and heated. The results of this are also pictured bellow. I expected iron hydroxide then iron oxide to appear, but instead a blackish-blue precipitate appeared along side some red iron oxide. When ~32% hydrochloric acid was added to this precipitate it dissolved to form a yellow solution free of undissolved material.


[Edited on 2-6-2018 by VSEPR_VOID]

Dried .JPEG - 231kBPrec.JPEG - 175kB

wg48 - 2-6-2018 at 05:37

Some tape cassette player motors have what I believe is a mu-metal sleeve on them. see the pic below. I have not chemically confirmed that the sleeve contains a significant percentage of nickel. Of cause these days it may be hard to find an old tape cassette player.

The grey material under the label is the mu-metal or some other high mu magnetic screening material

pKbdP.jpg - 42kB

VSEPR_VOID - 2-6-2018 at 06:22

I could swear I have seen metal ribbons around the casing like that on other motors. Is it specifically that one type of motor?

Capture.PNG - 177kB

wg48 - 2-6-2018 at 13:21

Quote: Originally posted by VSEPR_VOID  
I could swear I have seen metal ribbons around the casing like that on other motors. Is it specifically that one type of motor?


No its for any motor that may interfere with what ever the motor is in. I have also seen L shaped sheets above turntable motors and open-ended boxes over mains transformers, which I assumed were mu metal.

One motor I have is like yours and it has a sleeve on it but I think it was from a vacuum cleaner. The shield is a dull grey colour similar to the mu metal shields on oscilloscopes tubes. It is not like the silver shiny main body of the motor. But why use Mu metal for a vacuum cleaner motor?

So rather than mislead you I cut a small piece off the shield and a small piece of zinc plated steel. I put both in test tubes containing 28% HCl. Both are vigorously bubbling. I conclude that both are mostly iron. So I now doubt if any of those small motors have Mu metal shields. I have a very fancy tape drive for data storage but modern hard drives have made it redundant. Its got a nice case I could use so I will check its motors at some point when it get dismantled.

I just checked the test tubes again both are in a water bath at about 60C. Both look very similar vigorously bubbling and the both solutions are a light slight greenish yellow colour. If anything the soft iron is bubbling a little more.


NEMO-Chemistry - 2-6-2018 at 13:43

I posted a while back about Nickel, i had flakes and wanted chloride. I thought i had failed because i got something the wrong way around!!

I used ferric chloride acidified with HCL (your supposed to also add a Amine for speed) I did post a reference somewhere for this i think its in refs, and i am pretty sure its from the JCE.

It dissolves slowly without a AMINE, but when i added ammonia it formed a kind of 'gloop' i thought tjhis was iron from the ferric chloride at the time and threw it away.

The solution looked very dark and some (a fair bit) of Nickel was left in the tube. I let mine react for 5 days!!! but i am told if you add the amine and gently heat then its just a few hours.

When i added water i did get a greenish colour so maybe it did work!! I will try again tomorrow as i could really use some Nickel Chloride to do some plating.

I did a quick search but cant find my post, i am also fairly sure its one the few experiments i took a few pics of, trust me dissolving Nickel is not a spectator sport!

Sorry it was a web page i got it from, isnt the guy a member here?

http://lanthanumkchemistry.over-blog.com/article-the-dissolv...
and another
https://link.springer.com/article/10.1007%2FBF00728908


[Edited on 2-6-2018 by NEMO-Chemistry]

VSEPR_VOID - 2-6-2018 at 18:58

I went looking and found a motor from I think a printer that had one of those metal sleeves on it. It was easy to remove with a knife. It is not easily bent and is a dull grey. I will get some more H2O2 tomorrow and try to dissolve it.

There is a brand of pool hydrogen peroxide at my local publix that is 10% strength. I am considering trying to concentrate it.

I left out the yellow crystals in sunlight, in a clear jar with a desiccant, to dry and they turned yellow. I am sure this is the result of ferrous chloride oxidizing somehow back to the ferric salt. This makes me rather sad as I enjoyed the original color.

wg48 - 2-6-2018 at 21:15

Quote: Originally posted by VSEPR_VOID  
I went looking and found a motor from I think a printer that had one of those metal sleeves on it. It was easy to remove with a knife. It is not easily bent and is a dull grey. I will get some more H2O2 tomorrow and try to dissolve it.

There is a brand of pool hydrogen peroxide at my local publix that is 10% strength. I am considering trying to concentrate it.

I left out the yellow crystals in sunlight, in a clear jar with a desiccant, to dry and they turned yellow. I am sure this is the result of ferrous chloride oxidizing somehow back to the ferric salt. This makes me rather sad as I enjoyed the original color.


Cut a small peice off and see if it desolves in plain HCl before you start with H2O2/HCl to check if its soft iron.

VSEPR_VOID - 3-6-2018 at 23:21

Quote: Originally posted by wg48  
Quote: Originally posted by VSEPR_VOID  
I went looking and found a motor from I think a printer that had one of those metal sleeves on it. It was easy to remove with a knife. It is not easily bent and is a dull grey. I will get some more H2O2 tomorrow and try to dissolve it.

There is a brand of pool hydrogen peroxide at my local publix that is 10% strength. I am considering trying to concentrate it.

I left out the yellow crystals in sunlight, in a clear jar with a desiccant, to dry and they turned yellow. I am sure this is the result of ferrous chloride oxidizing somehow back to the ferric salt. This makes me rather sad as I enjoyed the original color.


Cut a small peice off and see if it desolves in plain HCl before you start with H2O2/HCl to check if its soft iron.


The metal reacts with dilute hydrochloric acid so it probably either iron or covered in zinc (which is my bet). Most electronic casings tend to be plated in a thin layer of zinc metal to protect against corrosion.

Left most beaker: The original salt after drying. Notice it turned back to yellow-brown indicating the ferrous salt oxidized.

Middle beaker: The result of treating a solution of the salt with large amounts of concentrated ammonia. The precipitate was filtered, washed with water, and is being dried.

Right test tube in beaker: Magnatite (Fe3O4) which was confirmed by placing a magnet near it. This was made by treated the salt with concentrated sodium hydroxide.


Conclusion

The brackets in the hard drive are almost entirely iron with trace amounts of what is possibly nickel. This was an interesting exercise known the less. I recommend that the SM wiki be changed to include this information. For future study I will continue to investigate the "mu-metal" cover of motors.

20180604_020730.jpg - 711kB20180604_021621.jpg - 649kB

Mabus - 4-6-2018 at 09:34

@VSEPR_VOID I have tried to find the information where I found the mention of Mu-metal being used in hard drive brackets, but so far haven't found much.
I did find, however, this thread on the Goldrefiningforum, where a person tested some hard drive brackets with nitric acid, and compared the result with a few nickel pennies. Apparently the silvery ones are nickel alloy. Somebody there also mentioned that Mumetal was also used in the outer frames of some old computers and hard drives. I have encountered many old hard drives with some flat plates of various forms, but I've not collected them since some were magnetic and others were not, so I just assumed they were some stainless steel (they also didn't rust easily).
Also, he sent one sample to analysis:

Quote:

ANALYSIS UPDATE:

On my huge heavy neo magnet holder plates. The ones I had were 10mm thick, and were curved like a C shape to accomodate the two large neos.
Confirmed that they are Mu-metal, and indeed have nickel in them, but mostly on a very thin surface layer.
I took the lot (about 30kg) to a local recycler to analyse with test gear.
They tested surface and found 85/15 nickel/iron %, and cut in half, tested center to find 2/98 nickel/iron %, and the same with a micron abraded surface.

So there you go, mostly iron with 2% nickel, and a fine surface layer of nickel, probably there to simply protect the iron from rusting.

These figures are from *MY* Mu-metal pieces, and are quoted from memory, I have exact written down somewhere and will edit when and if I can.

I got about NZ$16 for the iron content, with the nickel classed as a contaminant!

SK

That's not a lot of nickel, not sure if it was because those brackets were huge. I'd really like to see what would be the percentage of nickel for laptop hard drive brackets, since those are very thin, where it'd be simpler for them to be Mumetal than a thin sheet of iron with Mumetal plating.

VSEPR_VOID - 4-6-2018 at 13:34

That sounds about right and my results support his findings. Mostly iron. I hope the motor metal coverings prove to be more interesting.

Bezaleel - 8-6-2018 at 06:58

Maybe slightly of-topic, but when you're after nickel, why don't you try a pottery supplies shop and look for black nickel oxide. This oxide has the approximate formula Ni2O3. It is a cancerous substance, so take care when handling it.

Black nickel oxide dissolves only in strong HCl solution on heating. No reaction with H2SO4 whatsoever, or with oxidising acids, like HNO3.

VSEPR_VOID - 8-6-2018 at 11:14

I would prefer not to buy it. It seems a bit like cheating.