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#1
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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 |
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#2
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| Steve H wrote: 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 [Only registered users see links. ] |
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#3
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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. |
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#4
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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). [Only registered users see links. ] (Steve H) wrote in message news:<7a78d452.0402041031.62a58208@posting.google. com>... |
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#5
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| [Only registered users see links. ] (Steve H) wrote: 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 |
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#6
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| 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. |
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#7
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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. ----== Posted via Newsfeed.Com - Unlimited-Uncensored-Secure Usenet News==---- [Only registered users see links. ] The #1 Newsgroup Service in the World! >100,000 Newsgroups ---= 19 East/West-Coast Specialized Servers - Total Privacy via Encryption =--- |
| Tags |
| chloride , ferric , home , regen |
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| Thread | Thread Starter | Forum | Replies | Last Post |
| Making a small quantity of ferric chloride (III) | Patrice Nadeau | Chemistry Forum | 14 | 01-30-2004 01:59 AM |
| Sir William Crookes and the New Force | Majestic | Chemistry Forum | 0 | 11-24-2003 04:37 AM |
| Dissociation constant of ferric chloride (or solubility product) | Simon Dexter | Chemistry Forum | 1 | 10-15-2003 02:23 AM |
| ferric chloride | Steve Turner | Chemistry Forum | 1 | 08-05-2003 01:11 AM |