New Catalysts Turn the Greenhouse Gas Methane Into Valuable Chemicals

Researchers developed a novel catalyst that converts methane into valuable chemicals more sustainably, potentially advancing efforts to decarbonize the chemical industry.

Methane, a potent greenhouse gas, plays a crucial role both as an energy source and a vital chemical feedstock. Typically, methane undergoes conversion into methanol before being transformed into hydrocarbons. This process, however, demands elaborate industrial systems. Crucially, because methane is a highly stable molecule, converting it into methanol through traditional methods like steam methane reforming is highly energy-intensive.

Against this backdrop, the catalytic conversion of methane into methanol or other chemicals has attracted much attention from scientists, who are eager to find more energy-efficient and sustainable solutions. Among recently reported catalysts, copper (Cu)-containing zeolites have shown promise for methane-to-methanol conversion at mild conditions. Unfortunately, the yield and selectivity of most reported catalysts have been low, meaning that large quantities of undesirable byproducts are generated alongside methanol.

In a recent study published in the journal Nature Communications, a research team including Associate Professor Toshiyuki Yokoi from Tokyo Institute of Technology, Japan, investigated a new type of bifunctional zeolite catalyst. Interestingly, this Cu-containing, aluminosilicate-based zeolite is capable of converting methane and nitrous oxide, another greenhouse gas, directly into valuable compounds through a series of intermediate reactions.

Optimizing Catalyst Structure for Enhanced Output

One of the key questions the researchers addressed was how the spatial distribution of different active sites in the catalyst affected the output of the reactions. To this end, they prepared multiple catalysts using not only different concentrations of Cu and acid sites (proton) in aqueous solutions but also different physical mixing techniques for solid samples.

Through various experimental and analytical techniques, the researchers found that the proximity between Cu and acid sites was crucial for determining the final products. More specifically, they reported that when Cu sites were near each other, the methanol produced in Cu sites from methane had a higher probability of being overoxidized by an adjacent Cu site, turning it into carbon dioxide. In contrast, when Cu sites and acid sites were close to each other, methanol reacted with nitrous oxide in an adjacent acid site instead to produce valuable hydrocarbons and harmless nitrogen gas.

“We concluded that, for stable and efficient production of methanol and ultimately useful hydrocarbons from methane, it is necessary to uniformly distribute Cu sites and acid sites and have them be at an appropriate distance from each other,” explains Yokoi. “We also found that the distribution of products obtained is also influenced by the acid properties and pore structure of the zeolite catalyst.”

One of the most notable advantages of the proposed catalyst is its ability to sustain tandem reactions, that is, a simple process that merges multiple steps into one and gets rid of two different harmful greenhouse gases simultaneously. This property will be key to making such catalytic systems attractive in an industrial setting.

“Our work will hopefully guide future efforts to achieve methane oxidation to methanol and open avenues for promoting hydrocarbon synthesis using methanol as an intermediate,” concludes Yokoi.

With any luck, this study will serve as a stepping stone toward the decarbonization of the chemical industry, contributing to the realization of a carbon-neutral society.

Reference: “Understanding the effect of spatially separated Cu and acid sites in zeolite catalysts on oxidation of methane” by Peipei Xiao, Yong Wang, Lizhuo Wang, Hiroto Toyoda, Kengo Nakamura, Samya Bekhti, Yao Lu, Jun Huang, Hermann Gies and Toshiyuki Yokoi, 28 March 2024, Nature Communications.
DOI: 10.1038/s41467-024-46924-2

The study was funded by the Japan Society for the Promotion of Science.

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