I. Experiments with a kiln.
Considering the fundamental importance of heat as an agent in chemistry, I think that a kiln is a good general-purpose instrument that deserves to be in the possession of every school. They range quite a bit in size, maximum temperature, and power requirements, but even a small one will enable you to perform a variety of activities involving pottery, glass, minerals, and metals. Our school recently bought a Paragon Firefly model from Clay King for a bit over $300. It is quite small, which means we can’t fire large objects or many objects simultaneously, but it also means we can power it with a normal wall outlet, and we can use it indoors in a large well-ventilated room.
The rest of this post is a description of several experiments involving metals in kilns, including a method I developed for smelting metals in a kiln. If you do not wish to purchase a kiln, you may be able to sweet-talk a local college art department or ceramics studio into letting you use one of theirs. The homeschooling-ideas website also presents several interesting homemade alternatives to kilns.
II. The weathering of metals.
Before we get to smelting, what about just putting plain metals in the kiln, and baking them until they glow? The following picture shows what pennies, nickels, and dimes looked like after I baked them to about 2000F. They all deteriorated and formed a sort of flaking-off crust–black or dark gray in the case of the copper pennies, grayish or greenish in the case of the nickels, and grayish in the case of the dimes. (Nickels and dimes are a combination of nickel and copper.) In a separate test, I also tried steel, in the form of paperclips and steel wool, and the same thing happened–the paperclips turned into a black and brittle material, and the steel wool crumbled into black dust in my hands. In all of these examples, the extreme heat turned the metals into something very un-metal-like, something brittle and crumbly and that can be turned easily into powder. We call this formerly metal material *calx*.
Note that the bowls were homemade, using clay from the pottery supply store, dried and baked to about 1900F. You could just as easily use the clay trays that go under clay flower pots, as long as they are undecorated and you remove the price sticker.
Also note that the pennies were pre-1982 pure copper pennies. In the early 80s, the copper in pennies became more valuable than the pennies, i.e. the copper in one penny was worth more than one cent, so the U.S. Mint started making pennies out of cheaper zinc, and coating them with copper to make them look like copper. Apparently 1982 was a transitional year, and all pennies dated 1983 or later are mostly zinc. I strongly recommend that you sort your pennies and do not put any new zinc pennies in a kiln above about 1700F, because this is what happens when you do:
The zinc pennies, just like the other coins, turn into a calx, but in the case of zinc, the conversion is so complete and so vigorous that it ends up as white powder all over the place. The picture above actually shows the second time that I tried putting zinc pennies in the kiln, in which case I placed the bowl containing the pennies within a clay flower pot and placed a clay tray over the top as a lid. What are apparently metal vapors nevertheless seeped out the bottom and through the cracks and ended up piling into cotton-candy like billows of white fluff. This messy calcification of zinc would not by itself be a problem–the white calx is easily swept up or blown away. Unfortunately, there is something else going on that I don’t understand. There is some sort of yellowish form or mixture of the deteriorating zinc that is corrosive, and can dissolve firebrick. My kiln now has some pits and eaten-away spots in the floor and interior walls, thanks to this. This is the reason I do not recommend putting new pennies in a kiln.
Here are two more metals you should not put in a kiln: lead and aluminum. Lead is cheaply available in the form of lead fishing weights, but I have never tried putting lead in a kiln, and I insist that you do not, either. THE CALX OF LEAD IS HIGHLY TOXIC, by inhalation as well as by ingestion, and if it does what zinc does, you would effectively be poisoning the air in your kiln room. DO NOT PUT LEAD IN A KILN. Aluminum is cheaply available in aluminum foil, and actually, I have no idea what would happen to it in a kiln. I suspect it would behave something like zinc, but I’ve never tried it.
By the way, metals turn to calx whether or not they melt. Zinc and tin both have very low melting points as metals go, and will melt easily in the kiln (or a torch flame). Nevertheless, they will calcinate as well, and if you try to puddle them in a bowl in your kiln, they will both melt below 1000F, but will form a sort of corroded, contorted lump of crustified metal in the bottom of your tray or bowl. (Tin is the main ingredient in lead-free “silver solder”, which you can buy at a hardware store.)
In any case, to return to the general process of calcination of metals, this seems to be a universal degredation that fouls most metals. The only metals that do not calcinate, or at least are much harder to calcinate, are the “noble” metals–gold, silver, platinum. Calcination is a general characteristic of the non-noble “base” metals. Another very similar characteristic of the base metals is that they degrade and turn to powder or crusty flakes when exposed to the *weather*. Iron and steel turn into a red or orange rust, copper and bronze–sometimes used in roofs or statues–form an aqua-colored patina. As with the formation of calx, this does not happen to noble metals. In fact, this is one of the primary reasons that noble metals are so precious and valuable–they are incorruptible. All of the base metals are sooner or later corrupted into non-shiny, non-workable, comparatively useless materials. (Specially made metals like brass and stainless steel can resist corrosion pretty well, but they still degrade eventually.)
II. The un-weathering of metals.
What does all of this metallic corruption mean for us? Well, what is going to happen to any base metals exposed in nature or buried underground? Sooner or later, air, water, and heat, acting alone or in combination, are going to turn all metals into very un-metallic minerals. This explains why we almost never find raw metals in nature. There are only a few kinds of metals that we can find pure and metallic in nature (apart from the noble metals, mainly copper) and even those few that we can find raw are pretty rare. So where do we get the vast quantities of metal that our civilization relies on to make beautiful and durable things? Where do we get those special metals, like aluminum, that don’t even exist in nature?
The answer is that we un-corrupt them. We find them in nature in their calcinated, rusted, corroded, degraded, un-metallic form, and we resurrect them. The picture below shows a polished stone–an example of malachite. Technically it is a mixture of malachite (the green stuff) and tenorite (or malconite? anyway, its the black stuff). If you separate these materials and grind them into powder, you get a green powder which curiously resembles copper patina, and a black powder which curiously resembles copper calx. And, oddly enough, if you bake either one in a special way at around 2000F, like a phoenix from the weathered copper ashes, you get copper. We call this smelting. Malachite is an ore of copper, and you can smelt copper by baking ground malachite.
There are a couple of issues to clarify before we try, however. First of all, it would be very interesting to actually start from scratch and smelt copper from malachite that I have ground myself, but I have never tried it. Instead, I have done something much simpler and easier and bought purified ore powder from a pottery supply store. The official chemical name for the green powdered patina is “copper carbonate”, and the chemical name for the black copper calx is “copper oxide”. I found them both under these names at the pottery supply store in the “glaze chemicals” section, and I have successfully smelted copper from both of them (although the green copper carbonate seems like it might give cleaner copper for some reason.)
The second issue is how we bake the ore powder. How can baking make the metal go both ways? How can baking turn metal into calx, and also turn calx back into metal? What’s the difference? The difference is that we need another ingredient. Ancient people who discovered smelting by accident, and then performed it deliberately, always performed it deep within a fire or furnace, with plenty of charcoal around, and not much fresh air. We’ll have to create the same conditions if we want to reverse the calcination process in our kiln. We’ll have to simulate a smelting furnace within the kiln. Here’s how I did it….
III. Smelting in a clay pot.
We need to bake our ore powder mixed with something combustible in a closed container. I tried putting seed corn and popsicle sticks in with the ore powder, thinking they would turn to charcoal in the kiln. The seed corn worked–it turned to charcoal in the kiln and reduced the ore to metal–but it created a lot of smoke in the kiln room while it was boiling off the non-charcoal ingredients. (Actually it was kind of interesting to find charcoal in the shape of corn kernels afterwards.) The popsicle sticks made the entire building smell like smoke, disappeared completely, and failed to yield any metal. It would be much less smoky to start with charcoal in the first place, but I didn’t want to put “match lite” charcoal in the kiln, and I didn’t want to deal with the mess of crushing the briquettes. The answer I found is aquarium filter charcoal–it comes in convenient pellets in convenient pourable containers. It is even “activated”, which means it is extremely porous, which may or may not improve the smelting.
For the container, we need something that can withstand the temperatures of the kiln, and be sealed with a lid to keep out fresh air. You could make your own crucible from clay, but I find it is difficult to make a lid fit right. Clay pots from the garden supply store work perfectly–you can use the trays which are supposed to go underneath as lids. The only difficulty is that there is a drainage hole at the bottom of the pot, but you can plug this easily enough with a little clay. (I’ve been told that the automotive body filler “Bondo” would work perfectly for this–it dries in 5 minutes, it doesn’t shrink when it dries as clay does, it can withstand kiln temperatures, and perhaps you could even sculpt a concave depression at the bottom to better collect the liquid metal–but I’ve never tried it.) Just to be on the safe side, you should place the pot on another tray to collect anything that leaks out the hole. As an alternative to clay pots, you could also buy unglazed ceramic bowls and unglazed tiles for lids at the pottery store, almost as cheaply as clay pots.
The whole smelting kit looks like this:
The black pellets are the charcoal, and the green powder is the copper carbonate. The white powder is “tin oxide”, a purified powdered form of the tin ore “cassitterite”, also available at the pottery supply store. You can smelt it separately to make tin, or you can mix a little bit–maybe one part in six–with copper ore to make bronze. (If you mix lots of tin with a little copper, you make pewter, or something close to it.) In a clay pot with a plugged hole, mix the ore powders in the desired proportions. You can either stir the charcoal in to the powder or pour a layer on top of the powder. I suspect the latter does a better job with less charcoal, but I don’t really know yet. For a first attempt, I would add about half as many spoonfuls of charcoal as you have ore powder–if you find lots of leftover charcoal, you can use less next time. With the ore powder and the charcoal in the pot, place one saucer on top as a lid, and another underneath as a spill catcher. You can try to seal the cracks with clay to make it airtight, but I haven’t found it to be necessary, as long as you have plenty of charcoal inside, and I have no end of trouble trying to make a clay seal that doesn’t crack when it dries. You also have to allow some way for the ores to exhale their non-metallic part (i.e. for the “oxide” and “carbonate” portions to escape as carbon dioxide gas). All in all, I think it is best not to worry about sealing the pots, unless you get really good at smelting and pottery and you want to produce very clean ores as efficiently as possible. I just placed the lids squarely on top of the pots, and it worked fine.
With the powder and charcoal inside and the lid on top, place the crucible into the kiln and fire the kiln to 1950-2000F. If I open the lid of the kiln a crack and listen closely, I sometimes notice a bubbling sound near the end (the sound of the ores “exhaling”) and the cessation of the bubbling noise seems to be a pretty good indication that the smelting is done. I suspect that it only occurs with the carbonate ore, but I haven’t done a thorough series of experiments to establish the nature of the bubbling as a certainty.
After waiting for everything to cool, break the pot if necessary, dispose of the leftover charcoal, and you will usually find small dots and globs of metal adhering to the walls, and a few larger globs on the bottom. Sometimes a large puddle will have gathered at the bottom of the pot, but not always. The following picture shows a sampling of metal that I have smelted from ore powder with aquarium charcoal in clay pots. From left to right, they are bronze, copper, and tin. I used a barbeque grill brush to clean the larger bits of copper and bronze, but the tin came out already bright and shiny, for some reason.
I haven’t decided yet whether or how to get into the chemical details with students, but for you the teacher, here’s a summary: Extreme heat causes metals to combine with oxygen in the air to form the calx. To a chemist, a calx is an “oxide”. Weathering either causes the same thing, i.e. the combination with oxygen to form an oxide, or it causes the metal to combine with carbon dioxide in the air to form a “carbonate”. The patina that forms on copper and bronze is copper carbonate. The majority of metal ores are oxides, carbonates, or sulfides (the combination of metal with sulfur.) In extreme heat and relatively fresh air, i.e. in a kiln, they all remain or turn into an oxide. In the case of carbonates, the heat drives off the carbon dioxide and substitutes oxygen, and in the case of sulfides, the heat drives off the sulfur and substitutes oxygen. In all cases, extreme heat and fresh air will leave you with an oxide. (You can try this yourself with the green copper carbonate–put some in a clay dish in a kiln, and it will turn into the black copper oxide.) The way to prevent or reverse the formation of the oxide and leave only metal is to cut off all fresh air, and supply the ore with carbon (charcoal) instead. The carbon will not only use up any fresh air that leaks in by burning, but will also extract the oxygen from the ore, in effect “breathing out” the oxygen from the ore as it burns into carbon dioxide, and leaving pure metal behind.
IV. Casting metal.
I have tried re-melting my metals into molds to make pretty shapes out of them, but without much success so far. The problem is that you need to melt them without turning them back into calx. Again, you need to simulate the conditions of a fire by enclosing the metal and mold in a container, and smothering them with charcoal. Apparently, however, making an airtight seal becomes a much greater necessity this time, because my attempts produced more or less calcined metal, especially on the upper side, which was not protected by the walls of the mold, even though it was covered with charcoal. These two lumps of metal represent my attempts to mold a copper univalve seashell, and a bronze clamshell (notice the black copper calx around what was the upper end of the seashell):
If you wish to try, I suggest the following procedure: Make a mold by mixing equal parts Plaster of Paris (available at any home supply store) and silica (available at the pottery supply store), adding this powder to water until you make a paste, then using the paste to fill a small homemade ceramic bowl or a paper ketchup cup. While the plaster is still wet, press a shell (or whatever) into the plaster and leave it there. After the plaster dries, you should be able to gently nudge, twist, and wiggle the mold-forming object (known as the “pattern”) free without damaging the mold. If you used a paper ketchup cup as your mold container (or “flask”), peel it from the dried plaster so that it doesn’t burn in the kiln. Now fill the mold with your nuggets of smelted metal, place it in a clay pot, smother it with charcoal, place it in the kiln with a lid on top and a tray underneath, and fire the kiln hot enough to melt the metal (around 2000F for copper, a little less for bronze, 1000F should be plenty for tin). After it cools, you should be able to crumble the plaster fairly easily, and with luck you’ll be left with a metal casting in the shape of your pattern.
(You may find some interesting additional ideas on the subject of melting and casting metals, including backyard melting furnaces, at www.backyardmetalcasting.com.)