Scientists Turn Harmful Methane Into Methanol at Room Temperature

An illustration of the cage structures of two iron-based zeolites used in the study. The red and gold spheres (representing oxygen and iron, respectively) make up the active site. The cage structure, in gray, is formed of silicon, aluminum and oxygen. The blue sphere quantifies the size of the largest molecule that can diffuse freely in and out of the active site cage (the diameter of methane is ~4.2 Å).
Credit: Benjamin Snyder

A “tantalizing” ” principle borrowed from nature turns harmful methane into useful methanol at room temperature. A team of researchers from Stanford University and the University of Leuven in Belgium has further elucidated the process in a new study in a recent edition of Science.

The discovery may be an important step toward a methanol fuel economy with abundant methane as the feedstock, an advance that could fundamentally change how the world uses natural gas. Methanol – the simplest alcohol ­­– is used to make various products, like paints and plastics, and as an additive to gasoline. Rich in hydrogen, methanol can drive new-age fuel cells that could yield significant environmental benefits.

If natural gas, of which methane is the primary component, could be converted economically into methanol, the resulting liquid fuel would be much more easily stored and transported than natural gas and pure hydrogen. That also would greatly reduce the emissions of methane from natural gas processing plants and pipelines. Today, escaped methane, a greenhouse gas many times more potent than carbon dioxide, nearly negates the environmental advantages of natural gas over oil and coal. The team’s new study is their latest to advance a low-energy way to produce methanol from methane.

“This process uses common crystals known as iron zeolites that are known to convert natural gas to methanol at room temperature,” explains Benjamin Snyder, who earned his doctorate at Stanford studying catalysts to address key facets of this challenge. “But, this is extremely challenging chemistry to achieve on a practical level, as methane is stubbornly chemically inert.”

When methane is infused into porous iron zeolites, methanol is rapidly produced at room temperature with no additional heat or energy required. By comparison, the conventional industrial process for making methanol from methane requires temperatures of 1000°C (1832°F) and extreme high pressure.

“That’s an economically tantalizing process, but it’s not that easy. Significant barriers prevent scaling up this process to industrial levels,” said Edward Solomon, Stanford professor of chemistry in the School of Humanities and Sciences, and of photon science at SLAC National Accelerator Laboratory. Solomon is the senior author of the new study.

Keeping the zeolites on

Unfortunately, most iron zeolites deactivate quickly. Unable to process more methane, the process peters out. Scientists have been keen to study ways to improve iron zeolite performance. The new study, co-authored by Hannah Rhoda, a Stanford doctoral candidate in inorganic chemistry, uses advanced spectroscopy to explore the physical structure of the most promising zeolites for methane-to-methanol production.

“A key question here is how to get the methanol out without destroying the catalyst,” Rhoda said.

Choosing two attractive iron zeolites, the team studied the physical structure of the lattices around the iron. They discovered that the reactivity varies dramatically according to the size of the pores in the surrounding crystal structure. The team refers to it as the “cage effect,” as encapsulating lattice resembles a cage.

If the pores in the cages are too big, the active site deactivates after just one reaction cycle and never reactivates again.  When the pore apertures are smaller, however, they coordinate a precise molecular dance between the reactants and the iron active sites – one that directly produces methanol and regenerates the active site. Leveraging this so-called ‘cage effect,’ the team was able to reactivate 40 percent of the deactivated sites repeatedly – a significant conceptual advance toward an industrial-scale catalytic process.

“Catalytic cycling – the continual reactivation of regenerated sites – could someday lead to continual, economical methanol production from natural gas,” said Snyder, now a postdoctoral fellow at UC-Berkeley in the Department of Chemistry under Jeffrey R. Long.

This fundamental step forward in basic science will help elucidate for chemists and chemical engineers the process iron zeolites use to produce methanol at room temperature, but much work remains before such a process might be industrialized.

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