Tag Archives: nuclear fuel

Trapping gases left from nuclear fuels

A July 20, 2014 news item on ScienceDaily provides some insight into recycling nuclear fuel,

When nuclear fuel gets recycled, the process releases radioactive krypton and xenon gases. Naturally occurring uranium in rock contaminates basements with the related gas radon. A new porous material called CC3 effectively traps these gases, and research appearing July 20 in Nature Materials shows how: by breathing enough to let the gases in but not out.

The CC3 material could be helpful in removing unwanted or hazardous radioactive elements from nuclear fuel or air in buildings and also in recycling useful elements from the nuclear fuel cycle. CC3 is much more selective in trapping these gases compared to other experimental materials. Also, CC3 will likely use less energy to recover elements than conventional treatments, according to the authors.

A July 21, 2014 US Department of Energy (DOE) Pacific Northwest National Laboratory (PNNL) news release (also on EurekAlert), which originated the news item despite the difference in dates, provides more details (Note: A link has been removed),

The team made up of scientists at the University of Liverpool in the U.K., the Department of Energy’s Pacific Northwest National Laboratory, Newcastle University in the U.K., and Aix-Marseille Universite in France performed simulations and laboratory experiments to determine how — and how well — CC3 might separate these gases from exhaust or waste.

“Xenon, krypton and radon are noble gases, which are chemically inert. That makes it difficult to find materials that can trap them,” said coauthor Praveen Thallapally of PNNL. “So we were happily surprised at how easily CC3 removed them from the gas stream.”

Noble gases are rare in the atmosphere but some such as radon come in radioactive forms and can contribute to cancer. Others such as xenon are useful industrial gases in commercial lighting, medical imaging and anesthesia.

The conventional way to remove xenon from the air or recover it from nuclear fuel involves cooling the air far below where water freezes. Such cryogenic separations are energy intensive and expensive. Researchers have been exploring materials called metal-organic frameworks, also known as MOFs, that could potentially trap xenon and krypton without having to use cryogenics. Although a leading MOF could remove xenon at very low concentrations and at ambient temperatures admirably, researchers wanted to find a material that performed better.

Thallapally’s collaborator Andrew Cooper at the University of Liverpool and others had been researching materials called porous organic cages, whose molecular structures are made up of repeating units that form 3-D cages. Cages built from a molecule called CC3 are the right size to hold about three atoms of xenon, krypton or radon.

To test whether CC3 might be useful here, the team simulated on a computer CC3 interacting with atoms of xenon and other noble gases. The molecular structure of CC3 naturally expands and contracts. The researchers found this breathing created a hole in the cage that grew to 4.5 angstroms wide and shrunk to 3.6 angstroms. One atom of xenon is 4.1 angstroms wide, suggesting it could fit within the window if the cage opens long enough. (Krypton and radon are 3.69 angstroms and 4.17 angstroms wide, respectively, and it takes 10 million angstroms to span a millimeter.)

The computer simulations revealed that CC3 opens its windows big enough for xenon about 7 percent of the time, but that is enough for xenon to hop in. In addition, xenon has a higher likelihood of hopping in than hopping out, essentially trapping the noble gas inside.

The team then tested how well CC3 could pull low concentrations of xenon and krypton out of air, a mix of gases that included oxygen, argon, carbon dioxide and nitrogen. With xenon at 400 parts per million and krypton at 40 parts per million, the researchers sent the mix through a sample of CC3 and measured how long it took for the gases to come out the other side.

Oxygen, nitrogen, argon and carbon dioxide — abundant components of air — traveled through the CC3 and continued to be measured for the experiment’s full 45 minute span. Xenon however stayed within the CC3 for 15 minutes, showing that CC3 could separate xenon from air.

In addition, CC3 trapped twice as much xenon as the leading MOF material. It also caught xenon 20 times more often than it caught krypton, a characteristic known as selectivity. The leading MOF only preferred xenon 7 times as much. These experiments indicated improved performance in two important characteristics of such a material, capacity and selectivity.

“We know that CC3 does this but we’re not sure why. Once we understand why CC3 traps the noble gases so easily, we can improve on it,” said Thallapally.

To explore whether MOFs and porous organic cages offer economic advantages, the researchers estimated the cost compared to cryogenic separations and determined they would likely be less expensive.

“Because these materials function well at ambient or close to ambient temperatures, the processes based on them are less energy intensive to use,” said PNNL’s Denis Strachan.

The material might also find use in pharmaceuticals. Most molecules come in right- and left-handed forms and often only one form works in people. In additional experiments, Cooper and colleagues in the U.K. tested CC3’s ability to distinguish and separate left- and right-handed versions of an alcohol. After separating left- and right-handed forms of CC3, the team showed in biochemical experiments that each form selectively trapped only one form of the alcohol.

The researchers have provided an image illustrating a CC3 cage,

Breathing room: In this computer simulation, light and dark purple highlight the cavities within the 3D pore structure of CC3. Courtesy:  PNNL

Breathing room: In this computer simulation, light and dark purple highlight the cavities within the 3D pore structure of CC3. Courtesy: PNNL

Here’s a link to and a citation for the paper,

Separation of rare gases and chiral molecules by selective binding in porous organic cages by Linjiang Chen, Paul S. Reiss, Samantha Y. Chong, Daniel Holden, Kim E. Jelfs, Tom Hasell, Marc A. Little, Adam Kewley, Michael E. Briggs, Andrew Stephenson, K. Mark Thomas, Jayne A. Armstrong, Jon Bell, Jose Busto, Raymond Noel, Jian Liu, Denis M. Strachan, Praveen K. Thallapally, & Andrew I. Cooper. Nature Material (2014) doi:10.1038/nmat4035 Published online 20 July 2014

This paper is behind a paywall.

Finding out how silver escapes from tristructural-isotopic (TRISO) fuel particles

South African-born and Idaho-based researcher Isabella van Rooyen has solved a problem of longstanding interest to nuclear researchers according to a Jan. 3, 2014 news item on Nanowerk,

Some come to Idaho to travel the highways that lead to the Tetons, to Yellowstone, to small towns and big adventures. Idaho National Laboratory researcher Isabella van Rooyen came, all the way from South Africa, looking for a piece of silver 500,000 times smaller than a poppy seed.

The silver was somewhere inside irradiated tristructural-isotopic (TRISO) fuel particles — a safer, more efficient, next-generation nuclear fuel — the “poppy seed” in question. Break a TRISO fuel particle open and it looks like a jaw breaker on the inside. An outer shell of carbon coats a layer of silicon carbide, which coats the uranium center where the energy-releasing fission happens. These layers are meant to contain the radioactive products of fission, which includes little bits of silver. Containment of the radioactive material is built right into the fuel itself.

But it doesn’t always work perfectly. Occasionally, in just one or two out of 100 particles, silver escapes the center. It moves around the particle, and potentially gets out. Since the 1970s, scientists have been wondering exactly how this happens.
“I find it absolutely fascinating,” said Van Rooyen. She has been studying the TRISO-silver problem since 2006. “I have a natural tendency to know what is going on [inside the fuel].”

The Jan. 2, 2014 Idaho National Laboratory news release by Shannon Palus, which originated the news item, details how scientists saw the problem,

The silver seems to jump the silicon carbide layer as though by magic. There is no obvious point of exit, or forcible silver-shaped hole, to be found.  The transport mechanism that brings it from the inside out is a mystery that spans decades. It is a wrinkle in the plan to make TRISO the most efficient, and potentially the safest, fuel of the future.

In South Africa, Van Rooyen worked on a number of hypotheses for the TRISO problem. For example, did it piggyback out of the TRISO fuel particle attached to another element? Were there almost-too-tiny-to-see nanotubes forming in the silicon carbide layer?

One possibility seemed most probable to Van Rooyen. But to test it, to even begin to see if it was correct, she needed to be able to get a closer look. And she needed irradiated TRISO fuel.

Getting back to the notion of the irradiated tristructural-isotopic (TRISO) fuel particles being like a jawbreaker on the inside, i.e., made up of many layers, scientists have a term for the networks where each layer meets the next and where the grains that make up the layers align with each other, nanoroads. This concept inspired Van Rooyen’s approach (from the news release),

Could the nanoroads be the silver precipitate’s path out of the TRISO fuel particle? They do offer a path of lesser resistance, a point of potential weakness in the silicon carbide. The first step would be to see if silver could be found along these roads.

Van Rooyen’s method of investigation was a Scanning Transmission Electron Microscope operated by Yaqio Wu, a Boise State University research associate professor and instrument lead of the Materials and Characterization Suite at the Center for Advanced Energy Studies.  Somewhere along one of the nanoroad grain boundaries, Van Rooyen and Wu, along with materials engineer Tom Lillo, might be able to spot the silver precipitate.

“We were really like private investigators,” Van Rooyen said. The silver’s presence on the nanoroads — if that’s where it was — would be a lynchpin clue in the mystery.

After a year of patience and administrative work, she finally got her hands on actual, irradiated samples.

At a research briefing on the morning the team received the samples, they discussed the fact that they were looking for a needle in a haystack. For one, the bits of silver were so small. And not all TRISO particles emit silver. Would there even be silver in the specific sample they were looking at?

After years of exploring and discarding various hypotheses about the location of the silver, Van Rooyen and her team placed the irradiated TRISO particle under the electron microscope. This would be the closest, most careful look at the nanoroads in irradiated TRISO ever.

On that very afternoon, microscope operator Wu zoomed in and they found the silver precipitate. It was wedged at the intersection of two layers of TRISO coating, at the nanoroads between grains.

It was “an absolute wow moment,” said Van Rooyen. “We made such a commotion that people from other labs were coming to have a look.”

The journey is far from over. Next, Van Rooyen and her team will observe the silver to see how far it moves through the silicon carbide and try to determine exactly how it is able to get out. Time and hard work will tell if the nanoroads hypothesis is correct.

As is always the case, there’s the lead scientist and then there’s everyone else who helped make the discovery possible:

In addition to her colleagues Lillo and Wu, Van Rooyen would like to acknowledge Jim Madden for focused ion beam sample preparation; Jason Harp for isotope calculations; Joanne Taylor (Idaho State University); and Kristi Moser-McIntire (ISU) from CAES for their organization and support in the licensing of the CAES facility, which enabled the team to bring irradiated samples to the microscope.

Here’s an image of the TRISO particles,

INL leads research efforts to test advanced TRISO nuclear fuel, which has several layers of carbon and carbide that serve as the primary containment for radioactive material. Courtesy: Idaho National Laboratory

INL leads research efforts to test advanced TRISO nuclear fuel, which has several layers of carbon and carbide that serve as the primary containment for radioactive material. Courtesy: Idaho National Laboratory