New insights may lead to more efficient methods for collecting extra hydrogen, which can corrode and explode.
WASHINGTON, D.C., November 15, 2017 -- Excess hydrogen can cause problems in a variety of industries. It can corrode semiconductors, electronics, and nuclear fuel sitting in storage. It also poses an explosion hazard. To remove this extra hydrogen, chemists can use an organic compound called a hydrogen getter that chemically binds to several hydrogen atoms.
But sometimes, during this binding process -- called catalytic hydrogenation -- the partially hydrogenated products become volatile, melting and evaporating away before they can bind to more hydrogen atoms. Now, researchers have explored how and why this volatility varies during hydrogenation, suggesting that a previously underappreciated effect from carbon-hydrogen bonds in the molecule is the main culprit.
The new analysis, published in The Journal of Chemical Physics, from AIP Publishing, can help chemists identify the ideal conditions needed for catalytic hydrogenation so they can better remove excess hydrogen.
"This creates a model for the behavior of other organic getters, allowing us to predict their optimal operating temperatures and environments," said Long Dinh, a physicist at Lawrence Livermore National Laboratory.
Dinh and his colleagues focused on a getter called 1,4 bis(phenylethynyl)benzene, or DEB. To remove hydrogen, crystal flakes of DEB are mixed with catalysts in the form of solid pellets. The pellets are made from activated carbon -- whose porous structure provides abundant surface area -- coated with palladium nanoparticles. The palladium catalyst splits hydrogen molecules into hydrogen atoms, which can then bind to DEB and form carbon-hydrogen bonds.
DEB is a high-capacity getter, capable of binding with up to eight hydrogen atoms. Most researchers thought that as getters like DEB bind with more hydrogen atoms and enlarge, they become more volatile. At high operating temperatures, they can then vaporize away, drifting far from the catalytic pellets where there aren't any hydrogen atoms with which to bind. "You stop the hydrogenation process prematurely," Dinh said.
But the researchers found that in the first two steps of hydrogenation, when DEB forms two carbon-hydrogen bonds per step (the carbon-hydrogen bonds are created on opposite sides of the molecule's carbon chain), the molecule actually decreases in volatility. Only in subsequent steps of hydrogenation does DEB become more volatile.
To study how and why DEB changes in volatility, the researchers measured properties such as vapor pressures and melting points, probed molecular structure, and ran quantum mechanical computer simulations to model the hydrogenation process. Their analysis suggests that the carbon-hydrogen bonds in DEB play a key role in the molecule's volatile behavior.
During hydrogenation, hydrogen binds to carbon atoms in DEB. According to conventional thought, the resulting carbon-hydrogen bond is nonpolar -- neither end of the barbell structure is more negatively or positively charged than the other. But it turns out that the carbon end is slightly more negative, and the carbon-hydrogen bond forms a weak dipole, Dinh explained.
As a dipole, a carbon-hydrogen bond can attract or repel other carbon-hydrogen bonds in other DEB molecules. Depending on how the carbon-hydrogen bonds are arranged and how many there are in the intermediate DEB products, the molecules can either attract or repel one another, and thus be less or more volatile, respectively. Previous research had overlooked these collective interactions among carbon-hydrogen bonds in organic crystals, Dinh said.
From their analysis, the researchers determined that the optimal conditions for DEB hydrogenation is below about 175 degrees Fahrenheit, if done in a good vacuum. "Our results," Dinh said, "can be applied analogously to other catalytic organic hydrogen getter systems as well."
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The Journal of Chemical Physics
The Journal of Chemical Physics publishes concise and definitive reports of significant research in the methods and applications of chemical physics.