When I was a kid we used to go to a place we just called “The Book Barn.” It was pretty descriptive, as it was just a barn filled with old books. It smelled pretty much like you’d expect a barn filled with old books to smell, and it was a fantastic place to browse — all of the charm of an old library with none of the organization. On one visit I found a stack of old magazines, including a couple of Popular Mechanics from the late 1940s. The cover art always looked like pulp science fiction, with a pipe-smoking father coming home from work to his suburban home in a flying car.

But the issue that caught my eye had a cover showing a couple of rugged men in a Jeep, bouncing around the desert with a Geiger counter. “Build your own uranium detector,” the caption implored, suggesting that the next gold rush was underway and that anyone could get in on the action. The world was a much more optimistic place back then, looking forward as it was to a nuclear-powered future with electricity “too cheap to meter.” The fact that sudden death in an expanding ball of radioactive plasma was potentially the other side of that coin never seemed to matter that much; one tends to abstract away realities that are too big to comprehend.

Things are more complicated now, but uranium remains important. Not only is it needed to build new nuclear weapons and maintain the existing stockpile, it’s also an important part of the mix of non-fossil-fuel electricity options we’re going to need going forward. And getting it out of the ground and turned into useful materials, including its radioactive offspring plutonium, is anything but easy.

Lixiviants and Leachates

Despite its rarity in everyday life, uranium is surprisingly abundant. It’s literally as common as dirt; stick a shovel into the ground almost anywhere on Earth and you’ll probably come up with a detectable amount of uranium. The same goes for seawater, which has about 3.3 micrograms of uranium dissolved in every liter, on average. But as with most elements, uranium isn’t evenly distributed, resulting in deposits that are far easier to exploit commercially than others. Australia is the winner of this atomic lottery, with over 2 million tonnes of proven reserves, followed by Kazakhstan with almost a million tonnes, and Canada with 873,000.

While most of the attention uranium garners has to do with the properties of its large, barely stable nucleus, the element also participates in a lot of chemical reactions, thanks to its 92 electrons. The most common uranium compounds are oxides like uranium (IV) oxide, or uranium dioxide (UO₂), the main mineral in the ore uranite, also known as pitchblende. Uranite also contains some triuranium octoxide (U₃O₈), which forms when UO₂ reacts with atmospheric oxygen. The oxides make up the bulk of commercially significant ores, with at least a dozen other minerals including uranium silicates, titanates, phosphates, and vanadates being mined somewhere in the world.

Getting uranium out of the ground used to be accomplished through traditional hard-rock mining techniques, where ore is harvested from open-pit mines or via shafts and tunnels running into concentrated seams. The ore is then put through the usual methods of extraction that we’ve seen before in this series, such as crushing and grinding followed by physical separation steps like centrifugation, froth flotation, and filtration. However, the unique chemical properties of uranium, especially its ready solubility, make in situ leaching (ISL) an attractive alternative to traditional extraction.

ISL is a hydrometallurgical process that has become the predominant extraction method for uranium. ISL begins by drilling boreholes into an ore-bearing seam, either from drill rigs on the surface or via tunnels and shafts dug by traditional mining methods. The boreholes are then connected to injection wells that pump a chemical leaching agent or lixiviant into the holes. For uranium, the lixiviant is based on the minerals in the ore and the surrounding rock, and is generally something like a dilute sulfuric acid or an aqueous solution of sodium bicarbonate. Oxygen is often added to the solution, either via the addition of hydrogen peroxide or by bubbling air through the lixivant. The solution reacts with and solubilizes the uranium minerals in the ore seam.

ISL offers huge advantages compared to conventional mining. Although uranium is abundant, it’s still only a small percentage of the volume of the rock bearing it, and conventional mining requires massive amounts of material to be drilled and blasted out of the ground and transported to the surface for processing. ISL, on the other hand, gets the uranium into aqueous solution while it’s still in the ground, meaning it can be pumped to the processing plant. This makes ISL a more continuous flow process, as opposed to the more batch-wise processing methods of conventional mining. Plus, the lixiviant can be tailored to the minerals in the ore so that only the uranium is dissolved, leaving the rock matrix and unwanted minerals underground.

Reacting With Hex

Uranium dioxide (UO₂) is the primary endpoint of uranium refinement. It’s a dark gray powder; the so-called “yellow cake” powder, which is also produced by chemical leaching, is an intermediate form in uranium processing and contains a mix of oxides, particularly U₃O₈. Natural uranium oxide, however, is not especially useful as a nuclear fuel; only a few reactors in the world, such as the Canada Deuterium Uranium (CANDU) reactor can use natural uranium directly. Every other application requires the uranium dioxide to be enriched to some degree.

Enrichment is the process of increasing the concentration of the rare fissile isotope ²³⁵U in the raw uranium dioxide relative to the more abundant, non-fissile isotope ²³⁸U. Natural uranium is about 99.7% ²³⁸U, which can’t sustain a chain reaction under normal conditions, but with three fewer neutrons in its nucleus, ²³⁵U is just unstable enough to be fissionable under the right conditions.

Unlike refining, which takes advantage of the chemical properties of uranium, enrichment is based on its nuclear properties. Separating one isotope from another, especially when they differ by only three neutrons, isn’t a simple process. The vast majority of the effort that went into the Manhattan Project during World War II was directed at finding ways to sort uranium atoms, and many of those methods are still in use to this day.

For most of the Cold War period, the principal method for enriching uranium was the gaseous diffusion method. Uranium oxide is first turned into a gas by reacting it with hydrofluoric acid to form uranium tetrafluoride, which is then treated with fluorine to first yield uranium pentafluoride and finally uranium hexafluoride:

The highly volatile, incredibly corrosive uranium hexafluoride gas, or hex, is pumped at high pressure into a pressure vessel that contains a semi-permeable separator made from sintered nickel or aluminum. The pore size is tiny, only about 20 nanometers. Since the rate at which a gas molecule passes through a pore depends on its mass, the slightly lighter ²³⁵UF₆ tends to get through the barrier faster, leaving the high-pressure side of the chamber slightly depleted of the desirable ²³⁵U₆. Multiple stages are cascaded together, with the slightly enriched output of each stage acting as the input for the next stage, eventually resulting in the desired enrichment — either low-enriched uranium (LEU), which is in the 2-3% ²³⁵U range needed for civilian nuclear reactor fuel, or high-enriched uranium (HEU), which is anything greater than 20% enriched, including the 85-90% required for nuclear weapons.

These days, gaseous diffusion is considered largely obsolete and has given way to gas centrifugation enrichment. In this method, gaseous hex is pumped into a tall, narrow cylinder spinning in a vacuum at very high speed, often greater than 50,000 revolutions per minute. The heavier ²³⁸UF₆ is flung against the outer wall of the centrifuge while the lighter ²³⁵UF₆ migrates toward the center. The slightly enriched hex is pumped from the center of the centrifuge and fed into the next stage in a cascade, resulting in the desired enrichment. The enriched hex can then be chemically converted back into uranium dioxide for processing into fuel.

Made, Not Found

Unlike any of the other elements we’ve covered in the “Mining and Refining” series so far, plutonium is neither mined nor refined, at least not in the traditional sense. Trace amounts of plutonium do exist in nature, but at the parts per trillion level. So to get anything approaching usable quantities, plutonium, the primary fuel for nuclear weapons, needs to be synthesized in a nuclear reactor.

The main fissile isotope of plutonium, ²³⁹Pu, is made by bombarding ²³⁸U with neutrons. Each atom of ²³⁸U that absorbs a neutron becomes ²³⁹U, a radioactive isotope with a half-life of only 23.5 minutes. That decays via beta radiation to neptunium-239 (²³⁹Np), another short half-life (52 hours) isotope that decays to ²³⁹Pu:

The process of creating ²³⁹Pu from uranium is called “breeding.” From the look of the reaction above, it seems like a civilian nuclear reactor, with its high neutron flux and fuel rods composed of about 96% unenriched uranium, would be the perfect place to make plutonium. There are practical reasons why that won’t work, though, and it has to do with one little neutron.

Plutonium isn’t really enriched the way that uranium is. Rather, plutonium is graded by the amount of ²⁴⁰Pu it contains; the lower the concentration relative to ²³⁹Pu, the higher the grade. That’s because ²⁴⁰Pu tends to undergo spontaneous fission, releasing neutrons that could pre-detonate the plutonium core of the bomb before it’s completely imploded. Weapons-grade plutonium has to have less than 7% ²⁴⁰Pu, and the longer the reaction is allowed to continue, the more it accumulates. Weapons-grade plutonium can only cook for a couple of weeks, which means a civilian reactor would need to be shut down far too often for it to both generate power and synthesize plutonium. So, special production reactors are used to create fissile plutonium.

Once the fuel rods in a production reactor are finished, the plutonium is chemically separated from any remaining ²³⁸U and other contaminating fission byproducts using a long, complicated process of extraction. One such process, PUREX (plutonium uranium reduction extraction), uses nitric acid and a combination of organic solvents like kerosene to dissolve the uranium, plus aqueous solvents and reducing agents to solubilize the plutonium. Plutonium dioxide can then be reduced to metallic plutonium, for example by heating it with powdered aluminum. The resulting metal is notoriously difficult to machine, and so is often alloyed with gallium to stabilize its crystal structure and make it easier to handle.