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Author: Subject: Problem with pacification of Ni.
Peskatore
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[*] posted on 19-2-2012 at 05:43
Problem with pacification of Ni.


I try to make nickel sulphate threw put Ni pieces in concentrated H2SO4.
But nothing happens.
How can I brake this pacification?
Are there same problem if I use HCl?
Thanks for help.
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m1tanker78
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[*] posted on 19-2-2012 at 06:28


Use nitric acid instead or a mix of hydrogen peroxide and H2SO4 will get you there more quickly.

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cyanureeves
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[*] posted on 19-2-2012 at 07:07


i epoxied a canadian quarter to the bottom of a shampoo bottle filled with diluted hcl acid and hooked it up to a phone charger and had nickel chloride in no time.i got a nice yellow-green powder of nickel chloride,i learned from this site that the nickel anode needs to be on the bottom. i never could make it with the anode and cathode both on the surface,i forgot why. the green dissolved nickel will sit at the bottom and not mix with the top layer which can even be syphoned off if you use a clear bottle.
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[*] posted on 19-2-2012 at 07:33


Try heating the conc. H2SO4 with the nickel in it. Hot conc. H2SO4 is a powerful oxidiser and strongly attacks all metals except gold and the platinum group.
SO2 will be released, so work outside or under the fume hood.

If you want to dissolve nickel in HCl, you can either add H2O2 (simple and effective) or use the nickel as anode at the bottom of the vessel and a small piece of stainless steel as cathode at the top of the vessel. The nickel chloride solution, which is more dense than the HCl, stays at the bottom of the vessel and doesn't reach the cathode where it would otherwise be reduced back to nickel. Cyanureeves has already mentioned this.




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Peskatore
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[*] posted on 19-2-2012 at 07:34


Thanks. I mixed H2SO4 in little H2O2 solution and put the Ni in that. Its quickly solute and becomes green.
Unfortunately it also developed some nasty gas SO2, HS? But I have al my windows open now.
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Peskatore
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[*] posted on 19-2-2012 at 07:47


Another question. Are there any simple reagent solution making specific colour for Ni?
Its must give different colour from Fe.
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DJF90
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[*] posted on 19-2-2012 at 17:08


Ni content can be determined gravimetrically using the complex with dimethylglyoxime.
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cyanureeves
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[*] posted on 19-2-2012 at 17:21


ammonium hydroxide?
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LanthanumK
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[*] posted on 21-2-2012 at 06:48


Ammonia would also precipitate other metal hydroxides like Fe.



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Peskatore
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[*] posted on 22-2-2012 at 13:18


Hera are a test with K(Fe(CN6)), KSCN and amonia.
<a href="http://www.flickr.com/photos/77233366@N08/6921467925/" title="Fe-test-1 by Torulf, on Flickr"><img src="http://farm8.staticflickr.com/7039/6921467925_2904eae0c5.jpg" width="500" height="377" alt="Fe-test-1"></a>
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DougTheMapper
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[*] posted on 22-2-2012 at 16:38


Quote:
i epoxied a canadian quarter to the bottom of a shampoo bottle filled with diluted hcl acid and hooked it up to a phone charger


Now THAT's a facebook status.




Victor Grignard is a methylated spirit.
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cyanureeves
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[*] posted on 22-2-2012 at 18:37


Quote:
i epoxied a canadian quarter to the bottom of a shampoo bottle filled with diluted hcl acid and hooked it up to a phone charger.
it does read crazy. i meant to say that i stuck a quarter in half ways at the bottom of the bottle and epoxied it,then used it as an anode using a 5volt phone charger.

[Edited on 23-2-2012 by cyanureeves]
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Poppy
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[*] posted on 24-2-2012 at 19:15


doesphone chargers work by their own without overstanding currets?As for anhydrous acids they all work well when heated. I could e ven dissolve Fe2O3 in 85% H3PO4 at 1/2 mole ratio, the water insoluble rsulting salt took 2 days  to  precipitate

[Edited on 2-25-2012 by Poppy]
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cyanureeves
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[*] posted on 24-2-2012 at 19:24


yes phone chargers put out voltage 5v.3v 9v and 6v respectively they just dont put out alot of amperage but enough to work forever.simply clip the ends off and find the pos and neg with a voltmeter. i use them to electroplate with and even made small scale chlorate cells.it does not take hardly any voltage to dissolve metals in acid solutions.
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Poppy
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[*] posted on 24-2-2012 at 19:34


you sir mean chlorate accel parkerizing? we could share some information on that I got a useful recipe below

Attachment: 27920.pdf (496kB)
This file has been downloaded 1901 times

[Edited on 2-25-2012 by Poppy]

[Edited on 2-25-2012 by Poppy]o sorry you mean the cell matterial

[Edited on 2-25-2012 by Poppy]
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cyanureeves
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[*] posted on 25-2-2012 at 06:21


no Poppy. i mean i've made potassium chlorate but all my nickel plating that i have done looks like parkerized stainless steel. the shiny nickel plating is a whole other process with chromium and i havent had success with chrome plating but all my plating is done with phone chargers.i dont have a fancy plating machine.
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Poppy
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[*] posted on 25-2-2012 at 19:48


Im planning to dissolve some Ni too soon from the leftover of some stainless steel plates which are going to be cut at my gara ge till nexttime
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Peskatore
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[*] posted on 1-3-2012 at 11:19


I have an idea about making nickel sulfate with out sulfur acid.
Put metallic Ni in CuSO4 solution, Ni in surplus, and you get NiSO4.
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Poppy
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[*] posted on 8-3-2012 at 09:42


Pet,
I've just tried dissolving stainless steel at home, could not put a reaction to take place at cold, not sure yet whats in there, chromium or nickel. Its still left to try a pre-boiling water/acid mix, the electrocatalysed reaction and a decent acid for the purpose, and the CuSO4 idea of yours, of course.
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LanthanumK
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[*] posted on 9-3-2012 at 06:29


For stainless steel oxidation, make a stainless steel object the anode of a aqeuous NaCl electrolytic cell. You will get a massive amount of iron, chromium, and nickel hydroxides and discover that stainless steel is not so stainless after all. The resulting stainless steel object will be full of corroded pits.



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Poppy
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[*] posted on 10-3-2012 at 08:07


Any hints on explaing those many pits formed after corrosion?
Non smoothed alloys maybe?
As for electrolysis, small currents didn't seem to catalyse the process.
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