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This is a text from the PSI media archive. The contents may be out-of-date.
4 May 2017

Making a valuable resource usable with water

Media Releases Energy and Climate Research Using Synchrotron Light

New reaction for converting methane into methanol

In oil extraction sites, gaseous methane is simply burned, even though it could actually be a useful precursor material for fuels and products of the chemical industry. One way to make methane usable is to convert it to methanol. Being liquid, methanol is easier to transport than methane, and it can be used both as fuel and as raw material for the chemical industry. Researchers at the Paul Scherrer Institute PSI and ETH Zurich have now developed a new chemical process that allows this conversion in an efficient and inexpensive way. In the long run, this could be deployed in compact technical plants, which might also be set up in oil fields. The researchers report their findings in the latest edition of the journal Science.

Lead author of the Science paper Vitaly Sushkevich in his laboratory. (Photo: Paul Scherrer Institute/Mahir Dzambegovic)
Lead author of the Science paper Vitaly Sushkevich in his laboratory. (Photo: Paul Scherrer Institute/Mahir Dzambegovic)
PSI scientists Marco Ranocchiari (left) and Dennis Palagin, co-authors of the Science paper. (Photo: Paul Scherrer Institute/Mahir Dzambegovic)
PSI scientists Marco Ranocchiari (left) and Dennis Palagin, co-authors of the Science paper. (Photo: Paul Scherrer Institute/Mahir Dzambegovic)
Conversion from methane to methanol. (Photo: Paul Scherrer Institute)
Conversion from methane to methanol. (Photo: Paul Scherrer Institute)

The researchers have shown for the first time that methanol can be produced from a combination of methane and water. That is, to begin with, an important scientific discovery, stresses Marco Ranocchiari, a research group leader in the Laboratory for Catalysis and Sustainable Chemistry at the Paul Scherrer Institute PSI. Until now, it was not clear that water could be used to oxidise methane to methanol. At the same time, this process would also have significant advantages for industrial practice. Today, the conversion of methane to methanol takes place in two process steps, under high pressure and high temperature, in industrial chemical plants that are much too large and expensive to be set up on individual oil fields.

Direct conversion without unwanted by-products

In the reaction developed by PSI and ETHZ, the conversion is a direct process and takes place under lower pressure, so that much simpler plants can be realised. This reaction is not the first by which methane can be directly converted to methanol – PSI and ETHZ researchers have also had a hand in developing a number of other reactions. "The new reaction, though, is considerably more selective than the others", explains PSI researcher Dennis Palagin, one of the study's authors. That means the only by-product besides the methanol is hydrogen, which can for example be used for fuel cells. In the previously developed reactions, where for example oxygen or hydrogen peroxide is used for the oxidation, harmful substances such as carbon monoxide, CO2, or formaldehyde are produced as unwanted by-products.

Understanding the reaction through experimentation and supercomputing

In addition to methane and water, there is yet another active material involved in the new reaction. At the surface of this material, methane molecules are split into the constituents carbon and hydrogen, which then can bind together with water to form methanol and hydrogen. The active material has the structure of a zeolite in which copper atoms are embedded, and these play a crucial role in the reaction. "Thanks to a combination of different experimental methods, we were able to shed light on the mechanism behind the reaction", explains Vitaly Sushkevich, first author of the study, who designed the experiments. "For instance, we probed the reaction mechanism with infrared spectroscopy, and the changes in the copper with X-rays from PSI's Swiss Light Source SLS. To verify that the methane was in fact oxidised by the oxygen from the water, we selectively replaced part of the oxygen with another isotope and thus could follow its path. The experiments were complemented by theoretical calculations at the Swiss National Supercomputing Centre at Manno, in Ticino."

The research project was supported by funding from the Energy System Integration (ESI) Platform of the Paul Scherrer Institute.

Text: Paul Scherrer Institute/Paul Piwnicki


About PSI

The Paul Scherrer Institute PSI develops, builds and operates large, complex research facilities and makes them available to the national and international research community. The institute's own key research priorities are in the fields of matter and materials, energy and environment and human health. PSI is committed to the training of future generations. Therefore about one quarter of our staff are post-docs, post-graduates or apprentices. Altogether PSI employs 2000 people, thus being the largest research institute in Switzerland. The annual budget amounts to approximately CHF 370 million. PSI is part of the ETH Domain, with the other members being the two Swiss Federal Institutes of Technology, ETH Zurich and EPFL Lausanne, as well as Eawag (Swiss Federal Institute of Aquatic Science and Technology), Empa (Swiss Federal Laboratories for Materials Science and Technology) and WSL (Swiss Federal Institute for Forest, Snow and Landscape Research).

(Last updated in May 2016)

Contact
Prof. Dr. Jeroen van Bokhoven, Head of the Laboratory for Catalysis and Sustainable Chemistry, Division of Energy and Environment
Paul Scherrer Institute, 5232 Villigen PSI, Switzerland
Telephone: +41 56 310 50 46, e-mail: jeroen.vanbokhoven@psi.ch
Professor for Heterogeneous Catalysis, ETH Zurich, 8093 Zurich, Switzerland
Telephone: +41 44 632 55 42, e-mail: jeroen.vanbokhoven@chem.ethz.ch
Original Publication
Selective anaerobic oxidation of methane enables direct synthesis of methanol
V.L. Sushkevich, D. Palagin, M. Ranocchiari, J.A. van Bokhoven
Science 5 May 2017
DOI: 10.1126/science.aam9035

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