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Author: Subject: Copper Acetate Synthesis
redfish
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biggrin.gif posted on 1-1-2012 at 14:21
Copper Acetate Synthesis


Hello, everybody. This is my first post on the forum, so I will begin with an introduction.

I am a high school student with extremely limited access to... well, everything. While it is true that this is mostly due to the fact that I am too lazy to go out and get anything, I accept the challenge that absolute DIY presents. By "absolute DIY", I mean that I make EVERYTHING myself out of what is available, usually for culinary, first-aid, or general purposes. I own no labware- I salvage model paint jars, perfume tubes, pizza sauce jars, tin cans, tabasco sauce bottles, etc. for use in my chemical endeavors. I use a gas range and candles as heat sources. I don't even have any pipettes. Sure, I could buy some stuff, but I enjoy this challenge.

Now that you know where I'm coming from, I can explain WHY anybody would want to synthesize the target chemical, in this case Copper (II) Acetate. For me, this chemical is an important starting point, as it is one of the only soluble chemicals I can easily synthesize without appreciably large quantities of impurities such as sodium ions. Beyond that, it is a good source of Copper (II) ions and is a moderately strong oxidizing agent. This was one of the first chemicals I synthesized, and is very easy for beginners to synthesize.

There are two ways to approach this. The first, my original method, is more roundabout and less efficient, but it works and offers more practice for beginners. It is a three-part process. The second is more efficient and therefore should theoretically have a higher yield, although yields are fairly high in general; it is a two-part process.

First method, part 1
You will need a copper anode (pipe works, I used foil from a Li-ion battery), a copper or graphite cathode, batteries and wire, a container that can hold water, and water.

This part is pretty straightforward. Place the anode and cathode in the water, then hook up the battery's positive terminal to the anode and the negative terminal to the cathode. The greater the surface area of the anode, the better; also, the closer the electrodes are, the faster the process will occur.

You should see bubbles forming at the cathode. (Yes, this is Hydrogen gas, which is highly flammable and can be explosive but will generally only be produced in small quantities during this procedure.) This procedure is almost virtually identical to hydrolysis, with a single minor difference. The simplified equation for hydrolysis is:
2H2O(l)->2H2(g)+O2(g)
The simplified equation for hydrolysis with a copper anode is:
2H2O(l)+Cu(s)->H2(g)+Cu(OH)2(s)

The desired product from this reaction is the Copper Hydroxide, a light blue substance that forms on the anode and settles on the bottom of the container. If you use foil like I did, bits may break off in the water as the metal is oxidized; these can be filtered off in part 2. Over time, the hydroxide blackens as it decomposes into the oxide, CuO; this is also useable, so do not remove the black that forms. Some black CuO may also form on the cathode, if a copper cathode is used; since this is a useable chemical, shake this off into the water if you want maximum yield.

You can let this evaporate, boil it down, or carefully drain off the water to obtain the hydroxide, or you could just leave it in the water if you don't mind working with a more dilute solution in part 2.

First method, part 2
For this part, you will need the compounds formed in part 1, a sealable bottle or jar (an empty plastic disposable water bottle works fine), distilled white vinegar (other vinegars could work, but would include more impurities), filters (optional), and a sink.

To begin this part, transfer the compounds formed in part 1 to a sealable container, and fill with vinegar. (It should be safe to use excess vinegar, as it will evaporate with the water in the final concentration process.) The vinegar alone will not dissolve the hydroxide at room temperature; to form the acetate, the mixture must be heated. A convenient way to do this is to run the hot water in a sink, fill the sink in hot water, and immerse the container for a long time, changing the water occasionally. You should notice the solution becoming blue as you do this. Continue heating until all of the copper hydroxide and oxide has dissolved, and the solution is clear when agitated. If this is not the case after an hour of heating, add more vinegar if possible; if not possible, drain the solution (liquid) into another container and save, and then add more vinegar and continue heating. If solid metal flakes remain, they can be filtered off using coffee filters; impurities introduced by the vinegar can be minimized by passing the solution through an activated carbon filter.

Chemical equation for the reaction:
Cu(OH)2(s)+2CH3COOH(l)->2H2O(l)+Cu(CH3COO)2(aq)
and
CuO(s)+2CH3COOH(l)->H2O(l)+Cu(CH3COO)2(aq)

First method, part 3
This is the final part of the first method. For this part, you will need sealable plastic containers such as disposable water bottles and a freezer and/or an evaporating dish or large shallow bowl and/or a heat-safe dish and heat source.

This part concentrates on concentration (please pardon the pun). There are three methods that can be utilized here: freeze concentration, evaporation, and boiling. You may combine methods as you wish, but if a solid product is desired, I would recommend evaporation as a final step. Keep in mind that copper acetate is not very soluble in water, so a surprisingly small amount of solid will crystallize out of solution.

Boiling and evaporation are fairly straightforward. I often use the clear flexible plastic that some things are packaged in as evaporating dishes. When heating objects, make sure that you use a heat-safe container- I have broken many glass containers by heat contact, even if the heat source is only a candle. When boiling or evaporating, just use common sense.

Freeze concentration is another method that I would like to point out to budding chemists. It is often neater and easier than boiling and evaporation, and all you need is a freezer (or a cold climate) and a plastic bottle (water expands when frozen, so glass could shatter if used for this purpose). You also need another container with a mouth wider than the plastic bottle, to transfer the concentrated liquid into. All you have to do is, fill the plastic bottle about 3/4th's full of the solution, cap it, and stick it into the freezer. After a few hours, when it is completely frozen, take it out, unscrew the cap (this can be difficult, so feel free to use as much force as necessary), invert it, and stick it into the larger-mouthed container. The solution will melt faster than the water, and will drip into the container. This is the same method used when concentrating vinegar. Note, however, that this does not work due to a lower melting point of the solute, but rather because of the nature of hydrogen bonds in aqueous solutions of ionic or semi-ionic compounds.

Note that if you used excess vinegar in the creation of the copper acetate, it will likely be concentrated along with the salt after this part. Therefore, be careful when handling the final product, as it can be quite acidic.

Second method, part 1
For this method, you will need distilled white vinegar, a copper anode, a copper or graphite cathode, a battery and wires for hookup, and a container for the vinegar.

This part is nearly identical to part 1 of the first method, replacing water with vinegar. This is a much more efficient process. I noticed that more CuO formed on the cathode when electrolysing vinegar than water, so you may want to obtain max yield by scraping this off and heating it in the product solution, as in part 2 of method 1. However, this is not necessary, and will only slightly increase yield.

Second method, part 2
The final part of the second method is concentration. See part 3 of the first method.


Again, this is my first post so I could use some feedback.
Questions? Comments? Criticism?

[Edited on 1-1-2012 by redfish]
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Megak
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[*] posted on 1-1-2012 at 17:00


interesting, in my experience i've found electrolysis with copper electrodes to be tricky (with few exceptions).

What about this:
CuSO4 + 2CH3COOH -> Cu(CH3COO)2 + H2SO4

Though I doubt acetic acid would ever give up for sulfuric acid
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redfish
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[*] posted on 1-1-2012 at 17:32


Quote: Originally posted by Megak  
interesting, in my experience i've found electrolysis with copper electrodes to be tricky (with few exceptions).

What about this:
CuSO4 + 2CH3COOH -> Cu(CH3COO)2 + H2SO4

Though I doubt acetic acid would ever give up for sulfuric acid

What do you mean by "tricky"? It's no different from electrolysis using any other metallic anode.

And although that seems like it would make sense on first glance, remember that we are talking about ions in aqueous solution, so it's not that straightforward. You would just end up with Copper (II) ions, Hydrogen ions, Sulfate ions, and Acetate ions in solution. Besides, as I stated in my "introduction", I wouldn't have any copper sulfate to begin with. It would, however, increase the acidity of the solution. If there aren't any threads discussing why, I'd like to make one as it seems to be a topic of confusion (especially amongst high school chemistry students).
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theflickkk
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[*] posted on 1-1-2012 at 21:13



I've placed copper strips in a jar of acetic acid to make copper acetate. This method results in some small crystals of copper acetate forming around the copper strips that are partially submerged in the solution. Easy way to make copper acetate albeit rather slowly.
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redfish
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[*] posted on 1-1-2012 at 21:49


Quote: Originally posted by theflickkk  

I've placed copper strips in a jar of acetic acid to make copper acetate. This method results in some small crystals of copper acetate forming around the copper strips that are partially submerged in the solution. Easy way to make copper acetate albeit rather slowly.

Was the acetic acid you used glacial? I doubt this could happen using household vinegar, as copper is less reactive than hydrogen and therefore would not be easily oxidized by a 5% solution of acetic acid.
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[*] posted on 1-1-2012 at 23:48



Nope it was plain dilute acetic acid. Basically, artificial vinegar. I'm sure it works because i've done this many times. It takes a really long time to get a good crop of crystals though. With this method, you can just leave the entire container somewhere safe and return to "harvest" the crystals after some time (a long time actually).
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[*] posted on 1-1-2012 at 23:56


Ive got 2 videos of Copper Acetate Synthesis, both wih good yields... links are down below if you wanna check them out

Acetic acid, Copper, H2O2
http://www.youtube.com/watch?v=-aSaSe9x2E0&feature=plcp&...

Acetic Acid, Copper Carbonate
http://www.youtube.com/watch?v=znYJO7xa06s&feature=plcp&...




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redfish
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[*] posted on 2-1-2012 at 08:59


Thanks for the links, CA. The H2O2 and acetic acid method makes more sense to me, as the peroxide would aid in the oxidation of the copper, but I suppose you could get the same result from just the acetic acid if you let it sit for long enough. I'll have to try it myself sometime.

As for the carbonate, that's a more basic acid-base reaction. How do you make the carbonate, though? (I could do it in reverse, by adding copper acetate to a solution of sodium carbonate and collecting the precipitate, also producing the useful sodium acetate. But to use this to make more copper acetate would be redundant.)
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[*] posted on 2-1-2012 at 09:46


I made my Copper Carbonate by adding Sodium Bicarbonate to Copper Chloride or Copper Sulfate... Link below

Copper Sulfate, Sodium Bicarbonate
http://www.youtube.com/watch?v=4_z0pZe9eWg




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entropy51
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[*] posted on 2-1-2012 at 15:05


Must you start a redundant thread instead of searching for, finding, and adding to one of the existing threads?

For example http://www.sciencemadness.org/whisper/viewthread.php?tid=111...

in which Woelen gives a very simple synthesis from copper sulfate, available in hardware stores as root killer.

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[*] posted on 2-1-2012 at 20:05


Quote: Originally posted by entropy51  
[...] a very simple synthesis from copper sulfate, available in hardware stores as root killer.



Apparently you did not understand the purpose of this experiment. At the beginning of my post I explained that this procedure was designed so that any lazy bum (like myself) could perform it without making any purchases, owning any equipment not found in a 1/2 bath, or using any chemicals that could not be found in at least 90% of households.

I must admit that given this basis for this thread, it may have been more aptly created in the beginnings forum. However, since it deals with basic learning techniques and complete reagent synthesis, I believe that a separate thread is merited.
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[*] posted on 2-1-2012 at 20:13


Quote: Originally posted by redfish  
I believe that a separate thread is merited.
Well of course you did.



Better to remain silent and appear a fool than to open your mouth and remove all doubt.
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[*] posted on 2-1-2012 at 20:39


Haha yeah, you probably could have taken that for granted. I've got two books to read and a chemistry lab to finish for school tomorrow, so I need to redirect my attention towards my studies for now.
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[*] posted on 26-1-2014 at 09:48


You also can pass an electric current threw an aqueous solution of calcium acetate(Vinegar+egg shells or chalk) with 2 copper electrodes.

A second alternative would be to mix an equal ratio of H202 and vinegar and add copper metal

Here is a link to a video:
http://www.youtube.com/watch?v=mOpxpoOemN0

Good luck!
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