Nanosieves Save Energy In Biofuel Production

Daily Science Journal (Feb. 13, 2008) — A new type of membrane, developed by scientists of the University of Twente in The Netherlands, can stand high temperatures for a long period of time. This ‘molecular sieve’ is capable of removing water out of e.g. solvents and biofuels. It is a very energy efficient alternative to existing techniques like distillation.

The cylinder is the carrier of a hybrid membrane: a layer of about 100 nanometer thickness. The insert shows a close-up of the layer showing the organic links and pores. From the left of the tube, only water molecules leave the sieve. (Credit: Image courtesy of University of Twente)

Even after testing during 18 months, the new membranes prove to be highly effective, while having continuously been exposed to a temperature of 150 ºC. Existing ceramic and polymer membranes will last considerably shorter periods of time, when exposed to the combination of water and high temperatures. The scientists managed to do this using a new ‘hybrid’ type of material combining the best of both worlds of polymer and ceramic membranes. The result is a membrane with pores sufficiently small to let only the smallest molecules pass through.

Ceramic membranes, made of silica, degrade because they react with water and steam. In the new membrane, part of the ceramic links is therefore replaced by organic links. By doing this, water doesn’t have the chance to ‘attack’ the membranes. Manufacturing the new hybrid membranes is simpler than that of ceramic membranes, because the material is flexible and will not show cracks. What they have in common with ceramic membranes is the rapid flow: an advantage of this is that the membrane surface can be kept small.

The hybrid membranes are suitable for ‘drying’ solvents and biofuels, an application for which there is a large potential market worldwide. The main advantage of membrane technology is that it consumes far less energy than common distillation techniques.

The scientists also foresee opportunities in separating hydrogen gas from gas mixtures. This implies a broad range of applications in sustainable energy. Apart from that, the hybrid membranes are suitable for desalinating water. Using a hybrid membrane that is much smaller than the current polymer membranes, the same result can be achieved.

The results have been achieved in a close cooperation of scientists from the Inorganic Materials Science Group of the MESA+ Institute for Nanotechnology (UT), the Energy Efficiency in Industry department of ECN and the University of Amsterdam. The invention has been patented worldwide.

The article ‘Hybrid ceramic nanosieves: stabilizing nanopores with organic links’ by Hessel Castricum, Ashima Sah, Robert Kreiter, Dave Blank, Jaap Vente and André ten Elshof has been published in Chemical Communications (ChemComm) of the Royal Society of Chemistry in de UK.

Adapted from materials provided by University of Twente.

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Using Musical Chords To Analyze And Illustrate Hydrogen Molecule's Response To Laser Pulses

Daily Science Journal (Feb. 10, 2008) — For Kansas State University physics professor Uwe Thumm, confirmation of a theory about the behavior of small molecules became music to his ears -- literally. He and colleagues in Heidelberg, Germany, have shown how a hydrogen molecule responds to laser pulses by using the changing musical chord created by the molecule's vibrational motion.

Researchers in Heidelberg visualized the development over time of molecular resonance. The distance between the two nuclei (R) in the heavy hydrogen (deuterium) ion D2+ is plotted against the time. After approximately 100 femtoseconds, the wave packet, i.e. the location of the nuclei, starts to become hazy, after 400 femtoseconds there is a "revival" and the wave packet is put back together again. (Credit: Max Planck Institute for Nuclear Physics)

Thumm is a member of K-State's J.R. Macdonald Laboratory, where he is among several researchers who work on the properties and behavior of atoms and small molecules.

For decades, researchers had used the Macdonald Laboratory to make atoms and molecules collide with particles. Thumm said much of what scientists know about atoms and molecules is based on such collision experiments. To predict and explain what happens in these collisions, a large group of experimental physicists works closely with Thumm and two other theorists. The theorists use computers, make models and crunch numbers with the hope of producing results that are compatible with what experiments show.

Thanks to improvements in laser technology, around 1999 the Macdonald Laboratory researchers realized that they could transfer a lot of their expertise in atomic collisions to study in detail what happens when atoms and molecules get irradiated by very intense laser light. The new laser systems in the laboratory offer some advantages over the big particle accelerators, Thumm said. The laser pulses offer more control and can be made so short that the researchers now routinely observe the motion of nuclei inside small molecules in time. In addition, the laser pulses' peak intensity is enormous and would equal all of the sun's light focused onto a small spot of the size of a postage stamp or smaller.

Motivated by these opportunities, Thumm and his colleagues became curious about figuring out what would happen if the smallest and simplest molecule, hydrogen, were exposed to such ultra short and intense laser pulses. Together with his postdoctoral collaborator Bernold Feuerstein, Thumm developed a model and did calculations to determine how laser pulses influence the motion of the two protons in the hydrogen molecule.

"The short answer is that the laser pulse either makes the molecules vibrate more violently or blows them apart," Thumm said. He said this wasn't surprising because in the hydrogen molecule, two protons are connected by two electrons that function like a spring. When hit with the laser pulses, the protons oscillate back and forth.

Although this model may be easy to imagine on a large scale, Thumm said particles behave differently at the quantum level. This means that determining the locations of these oscillating protons isn't easy. Thumm described determining the protons' movements after being hit with the laser like what happens if you drop a marble in a bathtub. Looking at the circular ripples of water in the center of the tub, it's pretty easy to tell where the marble was dropped in. But when those ripples bounce off the sides of the tub, the wave pattern changes shape, and it becomes harder to tell where the marble was dropped. The wave gets delocalized. Thumm said the same thing happens to the protons not in a matter of seconds, but in a matter of femtoseconds -- that's a billionth of a millionth of a second. After about 60 femtoseconds, it's impossible to tell where the protons are.

"You quickly loose track of what the distance between the two protons is," Thumm said." All you can say is that they have a certain likelihood of being at a certain distance. This is in agreement with the bathtub experiment: Seconds after the marble was dropped, you can't tell where exactly it plunged in."

But things work differently at the quantum level, and the researchers were surprised that about 600 femtoseconds after being hit with the laser, the distance between the protons again becomes well defined. "We call this a revival of the original motion of the protons," Thumm said. "It's not going to happen in the bathtub, but it happens at the quantum level."

Thumm and Feuerstein published their theoretical prediction in 2003. Thumm said that they were pleasantly surprised when experiments at the Max-Planck Institute in Heidelberg, Germany, in 2006 confirmed the revival described in their model. "The agreement between the new experiments and our model was almost perfect and exceeded our expectations," Thumm said.

Feuerstein had since moved to Heidelberg, where he and his group of researchers continued to collaborate with Thumm's group at K-State. Excited about the success of their model, they began to analyze the molecule's vibrational motion by breaking it down into its various frequencies. Each frequency being like a note in a chord, the frequencies told researchers how the protons were behaving. However, the frequency of these molecular vibrations is way above the audible range. The two researchers share an interest in music and had collaborated musically before. So when it came time to illustrate the revival, they decided the best way to do it was to scale the frequencies down to 1,000 Hertz, which is in the range at which the human ear hears best. "This way you can listen to the vibrations and hear the revival. In the same way sound is analyzed and decomposed, we decomposed the vibration with regard to the frequencies," Thumm said. Their result, a changing musical chord coupled with a movie illustrating the protons' vibrations can be heard and viewed at http://www.mpg.de/video/FilmundoAudio-KdM.wmv

Thumm said researchers hope to be able to do the same thing for more complex molecules like water or methane. Just as a C Major chord sounds different from a d minor chord, Thumm said other molecules also would have their own unique sound. Thumm and Feuerstein's most recent work was first published last fall in the Physical Review Letters. Their research was supported by the National Science Foundation, the U.S. Department of Energy and the Max-Planck Society. Thumm said such basic research supports the long-term goal of applying lasers to steer chemical reactions. The hope is to largely increase the efficiency of chemical reactions by enhancing desired reaction pathways with lasers, he said.

Adapted from materials provided by Kansas State University.

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Magma And Volcanoes: Physicists Explain Dance Marathon Of Wispy Feature In Roiling Fluids

Daily Science Journal (Feb. 7, 2008) — Theoretical physicists at the University of Chicago are suggesting how thin spouts of magma in the Earth's mantle can persist long enough to form hotspot volcanism of the type that might have created the Hawaiian Islands.

University of Chicago physicists Wendy Zhang (left) and Laura Schmidt explain a feature of convecting fluids that colleagues have observed in laboratory experiments. The feature may help explain how hotspot volcanism created the Hawaiian Islands and other such landforms. (Credit: Dan Dry)

Their calculations also apply to tendrils only a few inches long that form in convecting fluids under laboratory conditions. University of Chicago graduate student Laura Schmidt and Wendy Zhang, an Assistant Professor in Physics, will detail their findings in the Feb. 1 issue of the journal Physical Review Letters.

The work was inspired by laboratory experiments conducted by Anne Davaille in France that mimic, in a simplified way, convecting bubbles of magma as they might look deep beneath the Earth's surface. "This is one robust feature of thermal convection," Zhang said.

"It's a useful thing to know because it's the kind of thing that happens in all sorts of different industries, in all sorts of different contexts." These include oil extraction, the chemical industry and in certain biotechnological applications.

Earth scientists also have theorized that mantle plumes form on a regional scale in the Earth's interior, sometimes breaking the surface to form small landmasses, including Hawaii and Iceland. Nevertheless, debate swirls around how, or even if, mantle plumes can account for such surface features.

Geophysicists often liken a pot of boiling water as a smaller, more rapid version of the convection that takes place in the mantle, the layer of Earth that lies between the surface crust and its core. But unlike a pot of water, the Earth's interior consists of layers with different properties.

In laboratory experiments, Anne Davaille, a geophysicist at the University of Paris 7, studies convection in a small tank by heating two layers of colored liquids of differing densities. She observed the formation and persistence of thin tendrils between the layers, which correspond to subsurface plumes measuring scores of miles across.

"It seems so thin and tenuous, how could it possibly manage to hold itself in place over time as everything else is going on around it?" Zhang asked. "Somehow, they manage to hold themselves together."

The tendrils persist for hours, even as experimental conditions change. "These tendrils have fluid flowing through them, and it starts to mix the two layers," Schmidt said. "When the two layers mix, then the viscosity of the layers changes as well."

Following a series of visits to Davaille's lab, Schmidt and Zhang sought to mathematically explain the phenomenon.

"When you look at the shape of these very thin tendrils, there's something very striking that Anne noticed right away," Zhang said. The tendrils seem to emerge from flow lines that resemble the flared-out end of a trumpet. This trumpet shape marked the location of a stagnation point. Both Davaille's experiments and Schmidt's calculations agree: The thinnest tendrils that persist have a stagnation point.

Schmidt had seen a similar stagnation point in experiments she conducted in the laboratory of Sidney Nagel, the Stein-Freiler Distinguished Service Professor in Physics at the University of Chicago. Those experiments involved unmixable fluids, such as water and oil, instead of the fresh water and salt water mixing in Davaille's laboratory.

Nevertheless, the experimental similarities provided Schmidt and Zhang insights that helped solve the problem. In previous studies, other theoreticians suggested how large flows might rise through the tendrils from the base of the hot spots, Schmidt said. She and Zhang approached the problem differently.

"We include the effect of the stagnation point," Schmidt explained. "Our tendrils are really a thin skin or thin layer of the surface between the fluids that is drawn up. It's not a bulk flow going up through the tendril."

Adapted from materials provided by University of Chicago, via EurekAlert!, a service of AAAS.

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New Nanotube Findings Give Boost To Potential Biomedical Applications

Daily Science Journal (Feb. 4, 2008) — Carbon nanotubes-cylinders so tiny that it takes 50,000 lying side by side to equal the width of a human hair-are packed with the potential to be highly accurate vehicles for administering medicines and other therapeutic agents to patients. But a dearth of data about what happens to the tubes after they discharge their medical payloads has been a major stumbling block to progress.

A representation of a carbon nanotube accessorized with a coating of branched PEG. (Credit: Courtesy of Hongjie Dai)

Now, Stanford researchers, who spent months tracking the tiny tubes inside mice, have found some answers.

Studies in mice already had shown that most nanomaterials tend to accumulate in organs such as the liver and spleen, which was a concern because no one knew how long they could linger. But fears that the tiny tubes might be piling up in vital organs, like discarded refrigerators at the bottom of a rural ravine, can now be put to rest, said Hongjie Dai, the J. G. Jackson and C. J. Wood Professor of Chemistry at Stanford, whose research team has demonstrated that the nanotubes exit the organs.

Dai and his group found that the carbon nanotubes leave the body primarily through the feces, with some by way of the urine. ''That's nice to know,'' Dai said. ''This now proves that they do get out of the system.''

The full extent of the news, which is scheduled to be published the week of Jan. 28 in Proceedings of the National Academy of Sciences Online Early Edition (PNAS), is even better than that: The three-month-long study also allays worries that the nanotubes, by simply remaining in the organs for a long time, would prove toxic to the mouse.

''None of the mice died or showed any anomaly in the blood chemistry or in the main organs,'' said Dai, senior author on the PNAS paper. ''They appear very healthy, and they are gaining weight, just like normal mice. There's no obvious toxicity observed.'' The lack of toxicity of nanotubes in mice is consistent with a previous pilot study done by Sanjiv Gambhir, a professor of radiology at Stanford, and his research group in collaboration with Dai's group.

''This is the first time anyone has done a systematic circulation and excretion study like this for nanotubes, and data on other nano particles is also scarce,'' Dai said. ''The excretion pathway may apply to other nano materials and may need to be looked at closely like this also.''

Previous research published by Dai's group has demonstrated the potential for using nanotubes in treating cancerous cells and targeting tumors in mice.

His group used Raman spectroscopy, a method of applying light from a laser beam that effectively ''illuminates'' the presence of the target molecules in the organs of the mice.

Being hit with light from the beam causes a detectable change in the state of a molecule's energy. Carbon nanotubes, composed entirely of carbon atoms that are mostly arranged in linked hexagonal rings, give off a strong signal in response to the beam. This allowed the researchers to pinpoint the position of the chosen molecules, as well as ascertain their abundance in the blood or organs.

Previous detection methods that relied on attaching fluorescent labels or spectroscopic tags to the nanotubes had yielded unreliable results. The attachments tended to either come loose from the tubes or decay over time spans ranging from a few days to only a few hours-far too short to reveal the ultimate fate of the nanotubes.

While knowing the carbon nanotubes will move through the digestive system at a healthy pace is critical to future practical applications, it is also crucial that the nanotubes not enter the digestive system too soon after being injected; they need to spend enough time in the circulatory system to find their way to their target location.

The key to fine-tuning the carbon nanotubes' speed of circulation turns on how the basic, bare-bones floor model is chemically accessorized.

''You can make the nanotubes circulate a very long time in the blood, if the chemistry is done right,'' Dai said. The researchers found that coating their carbon nanotubes with polyethylene glycol (PEG), a common ingredient in cosmetics, worked best.

They used a form of PEG with three little limbs sprouting off a central trunk. ''Those provide better shielding to the nanotube than just a single branch. Therefore, they interact less with the biological molecules around them,'' Dai said.

The team stuffed the PEG liberally into the linked hexagonal rings that compose the nanotubes, prompting Dai to describe the end result as resembling rolled-up chicken wire with feathers sticking out all over.

Though they may sound less than gorgeous visually, the feathery nanotubes turned in a beautiful performance in practical terms, Dai said. The coating of PEG made the nanotubes highly water soluble, which helped them to stay in the blood instead of being absorbed.

''They circulate in the blood for about 10 hours or so in mice, which seems to be a good length of time,'' Dai said.

The right chemical coating on nanotubes also can help ease them out of the mouse in a timely fashion, and the three-branched PEG was effective there, too.

Dai's earlier research demonstrated that nanotubes have promise for treating cancer with two different approaches. Once they have zeroed in on the target cells, shining light on the nanotubes causes them to generate heat, which can kill cancer cells. The other method is to rig the nanotubes to accumulate at targeted sites, where they can deliver medication from within the tubes.

''[Carbon nanotubes] seem to be promising for biomedical applications and for potentially treating cancer, either using drugs or using the physical properties,'' Dai said. ''This is the reason we carried out the study of the fate of nanotubes in mice. I think this is really a very fundamental issue.''

The research was funded by the Cancer Center for Nanotechnology Excellence, which is funded by the National Institutes of Health and the National Cancer Institute. The first author of the PNAS paper is Zhuang Liu, graduate student in chemistry. The paper's other authors, all affiliated with Stanford University, are Xiaoyuan ''Shawn'' Chen, assistant professor in radiology; Dr. Corrine Davis of the Veterinary Service Center in the Department of Comparative Medicine; Weibo Cai, postdoctoral scholar in radiology; and Lina He, formerly a technician in Chen's research group.

Adapted from materials provided by Stanford University.

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New Method For Creating Self-Assembling, Nanoscale Materials

Daily Science Journal (Feb. 2, 2008) — While biomedical, electronics, and other branches of research are marching steadily into the realm of the smaller-than-small nanometer scale, building needed materials at this scale has been problematic.

Recently, however, a team from The Scripps Research Institute unveiled a novel approach to the problem that yields a material with novel properties, which some might find reminiscent of Flubber. The material is produced using naturally occurring proteins as templates for uniform, self-assembled, nano-scale construction.

The material, an organic polymer described in today's early, online edition of the Proceedings of the National Academy of Sciences (PNAS), could one day find application in everything from screening for disease to microelectronics.

Using Nature's Tricks

Nature is replete with examples of molecules such as DNA that self-assemble with uniform patterns on the nanoscale, but until now researchers have had limited success duplicating such processes. The new study, however, provides one synthetic method that has effectively mimicked the templating strategy used in nature for nanoscale construction in the lab.

To create the new material, the Scripps Research team, led by Scripps Research President Richard Lerner and Assistant Professor Tobin Dickerson, began with a natural nanoscale product, a bacterial virus or phage. A nanometer is one billionth of a meter, or the width of a few average atoms.

Specifically, the product the team worked with was a phage known as M13. If scaled up, the phage is proportionally equivalent to a 4-foot-long pencil, with the tip and eraser roughly representing the active parts of the phage that infect bacteria. Other proteins that are biologically inert and analogous to the wood body of the pencil provide the filamentous phage's structure.

Having worked with phage extensively in other applications, the team decided to explore the possibility of using those structural proteins as a potential template for nanoscale construction. To do so, the team chemically modified molecular protrusions on the proteins so they would attract and bind with the components needed to form strands of polyacrylamide, a common polymer used to make laboratory gels.

The resulting polymer-phage combination, which twists into helices like DNA and RNA molecules, takes on the shape of a comb with the polymers as the teeth. These teeth in turn interlock to form a strangely resilient, rubbery solid.

Shocking Flexibility

Once the new material, known as a protein-polymer bioconjugate, was created, the group was shocked to find that it was almost impossible to break a sample apart. It could be sliced, but no matter how hard researchers compressed or squeezed it, it always bounced back to its original state, because the stable phage proteins act like rebar in concrete to provide strength.

Further analyses uncovered additional important characteristics. The combs do not grow completely uniformly—some combs grow more teeth than others, for instance, before interlocking with a nearby comb. But the combs can only be a prescribed distance apart for the chemical interlocking to occur, which leads to uniform size for the pores between the comb teeth. The pores proved to be about 4 nanometers wide and greater than 1 micrometer (one millionth of a meter) in length.

This uniformity is in stark contrast with experiments which showed that simply mixing the phages with polymers without the templating procedure produces a chaotic hodge podge at the molecular level.

Interestingly, after creating the material, the group discovered that a British scientist had done theoretical calculations about how flexible rods—like the phages—would pack together using the least amount of energy.

"It was extremely gratifying to see that the mathematics had exactly predicted what we were observing," says Dickerson

Putting It to Use

Although the work was intended mainly as a proof of concept for using the phages as templates, the researchers have a number of potential applications in mind. The phage can be produced easily and cheaply in very large quantities, and the polymer components are readily available and simple to combine to create the final material. These characteristics would make commercial application possible.

"In essence, bacteriophage-derived materials are a renewable resource," says Dickerson.

The defined channels established by the pores in the material might be adapted as pathways for electrons for use in microelectronics. Or, the pores might be used as a filter for certain molecules, for example to test blood samples for proteins whose presence is tied to particular diseases. More complex potential uses might include altering the biologically active portions of the phage to attract specific molecules, forcing them into the polymers' pores, or to block others.

"These tools can be visualized like Tinkertoys ® or Legos ®," says Dickerson of the possibilities. "You can think about this really in engineering terms using macroscopic analogs such as baskets, or lids, or holes."

To add to the list of potential applications, the team has already begun exploring additional materials that might be created using the basic phage construction scheme.

In addition to Dickerson and Lerner, authors on the paper, entitled "Biologically templated organic polymers with nanoscale order," were Bert Willis, Lisa Eubanks, Malcolm Wood, and Kim Janda, all of Scripps Research. See http://www.pnas.org/cgi/content/abstract/0711308105v1.

The work was supported by the Skaggs Institute for Chemical Biology, Worm Institute for Research and Medicine, and a National Institutes of Health Kirschstein National Research Service Award.

Adapted from materials provided by Scripps Research Institute.

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Researchers Create Gold Aluminum, Black Platinum, Blue Silver Using Tabletop Laser

Daily Science Journal (Feb. 2, 2008) — Using a tabletop laser, University of Rochester optical scientists have turned pure aluminum, gold. And blue. And gray. And many other colors. And it works for every metal tested, including platinum, titanium, tungsten, silver, and gold.

Gold Aluminum, Blue Titanium, Gold Platinum. (Credit: Richard Baker, University of Rochester)

Chunlei Guo, the researcher who a year ago used intense laser light to alter the properties of a variety of metals to render them pitch black, has pushed the same process further in a paper in today's Applied Physics Letters. He now believes it's possible to alter the properties of any metal to turn it any color—even multi-colored iridescence like a butterfly's wings.

Since the process changes the intrinsic surface properties of the metal itself and is not just a coating, the color won't fade or peel, says Guo, associate professor of optics at the Institute of Optics at the University of Rochester. He suggests the possibilities are endless—a cycle factory using a single laser to produce bicycles of different colors; etching a full-color photograph of a family into the refrigerator door; or proposing with a gold engagement ring that matches your fiancée's blue eyes.

"Since the discovery of the black metal we've been determined to get full control on getting metals to reflect only a certain color and absorb the rest, and now we finally can make a metal reflect almost any color we wish," says Guo. "When we first found the process that produced a gold color, we couldn't believe it. We worked in the lab until midnight trying to figure out what other colors we could make."

Guo and his assistant, Anatoliy Vorobeyv, use an incredibly brief but incredibly intense laser burst that changes the surface of a metal, forming nanoscale and microscale structures that selectively reflect a certain color to give the appearance of a specific color or combinations of colors.

The metal-coloring research follows up on Guo's breakthrough "black metal" discovery in late 2006, when his research team was able to create nanostructures on metal surfaces that absorbed virtually all light, making something as simple as regular aluminum into one of the darkest materials ever created.

Guo's black metal, with its very high absorption properties, is ideal for any application where capturing light is desirable. The potential applications range from making better solar energy collectors, to more advanced stealth technology, he says. The ultra-brief/ultra-intense light Guo uses is produced by a femtosecond laser, which produces pulses lasting only a few quadrillionths of a second. A femtosecond is to a second what a second is to about 32 million years. During its brief burst, Guo's laser unleashes as much power as the entire electric grid of North America does, all focused onto a spot the size of a needlepoint.

The intense blast forces the surface of the metal to form nanostructures—pits, globules, and strands that response incoming light in different ways depending on the way the laser pulse sculpted the structures. Since the structures are smaller than the wavelength of light, the way they reflect light is highly dependent upon their specific size and shape, says Guo. Varying the laser intensity, pulse length, and number of pulses, allows Guo to control the configuration of the nanostructures, and hence control what color the metal reflects.

Guo and Vorobyev also achieve the iridescent coloring by creating microscale lines covered with nanostructures. The lines, arranged in regular rows, cause reflected light of different wavelengths to interfere differently in different directions. The result is a piece of metal that can appear solid purple from one direction, and gray from another, or multiple colors all at once.

To alter an area of metal the size of a dime currently takes 30 minutes or more, but the researchers are working on refining the technique. Fortunately, despite the incredible intensity involved, the femtosecond laser can be powered by a simple wall outlet, meaning that when the process is refined, implementing it should be relatively simple.

The new process has worked on every metal Guo has tried, and the results are so consistent that he believes it will work for every metal known. His team is currently working to find the right tuning to create the rest of the rainbow for the solid-colored metal, including red and green.

Adapted from materials provided by University of Rochester.

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Diamonds Unlikely In Gas Giants Like Uranus

Daily Science Journal (Jul. 16, 2007) — A new study finds that diamonds probably don't crystallize in the atmospheres of planets such as Uranus and Neptune. The conclusion is contrary to recent speculation that small diamonds would spontaneously form in carbon rich layers of the gas giant planets. White dwarf stars, according to the study, are veritable diamond factories.

A simulated snapshot of crystallizing carbon atoms under Uranus-like conditions. (Credit: L. M. Ghiringhelli, C. Valeriani, E. J. Meijer and D. Frenkel, Physical Review Letters)

Physicists at the Universtiet van Amsterdam and the FOM Institute for Atomic and Molecular Physics in the Netherlands performed a numerical analysis showing that at the temperatures and pressures in gas giant planets like Uranus, arrangements of carbon atoms would be much more suitable for creating tiny bits of graphite rather than diamond.

In white dwarfs, on the other hand, the simulation shows that the conditions would cause the carbon atoms to line up in configurations that are much more amenable for diamond crystallization. The conclusion is consistent with the 2004 discovery of a cooling white dwarf star that appears to have a solid diamond core 4000 kilometers across.

Although diamond formation in the atmospheres of gas giants is not strictly impossible, the Dutch physicists say that the odds are exceedingly slim that a diamond could have formed under the conditions that exist in Uranus in the entire lifetime of the universe.

Adapted from materials provided by American Physical Society, via EurekAlert!, a service of AAAS.

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