Ultrastable, selective catalyst for propane dehydrogenation developed

Ultrastable, selective catalyst for propane dehydrogenation developed
On the surface of the newly developed catalyst (PtGa-Pb/SiO2), Pt1 sites remain exposed to facilitate catalytic reaction while Pt3 sites (and Ga3 sites) shown with triangles are blocked by Pb. Credit: Yuki Nakaya, et al., Nature Communications, June 5, 2020

A group of Japanese scientists has developed an ultrastable, selective catalyst to dehydrogenate propane—an essential process to produce the key petrochemical substance of propylene—without deactivation, even at temperatures of more than 600 degrees C.

Propylene is an important raw material for plastics, synthetic rubber, surfactants, dyes and pharmaceuticals. In recent years, there has been an increased demand for produced from cheaper, shale-originated propane. Reaction temperatures of more than 600 degrees C are necessary to obtain sufficient propylene yields, but under these harsh conditions, severe deactivation is inevitable due to carbon deposition and/or sintering. Catalysts in practical use, therefore, must be regenerated either continuously or in short cycles, making the process inefficient and costly.

In the present study, the group, including a master's student Yuki Nakaya and Associate Professor Shinya Furukawa at Hokkaido University's Institute for Catalysis, focused on the intermetallics (PtGa) of platinum (Pt) and gallium (Ga), which have unique properties and structures. PtGa has a high thermal stability and its structure does not change, even under high temperatures. It is also known to have two kinds of catalytic sites on its surface: a site with three Pt atoms (Pt3 site) and one with single-atom-like isolated Pt (Pt1 site).

The group hypothesized that if the Pt3 sites—which facilitate carbon deposition in addition to producing propylene—are disabled to allow only the Pt1 sites to function, the catalyst will be ultrastable and also able to prevent carbon deposition. The group tried various metals and catalyst synthesis methods to preserve only Pt1 function.

The newly developed catalyst (PtGa-Pb/SiO2), which is silica-supported and made by adding lead (Pb) to the surface of PtGa, exhibits no deactivation when dehydrogenating propane at 600 degrees C. The catalyst maintained the initial conversion rate of 30 percent for 96 hours after the reaction started, which is significantly more stable than conventional catalysts. Propylene selectivity is as high as 99.6 percent with few side reactions, including carbon deposition. The results showed that this catalyst produces the world's best performance at temperatures of 580 degrees C or higher. In particular, its is more than twice as long as the previous reported record longevity for such catalysts. Furthermore, the catalyst can be produced as cheaply as conventional catalysts. Their confirmed Pt3 sites, not Pt1 sites, were covered and disabled by Pb, as they expected.

"Our finding could lead to a more efficient and cheaper industrial process to produce propylene from propane without the need for catalyst regeneration—which is far superior in selectivity and stability than conventional ones," says Furukawa. "Moreover, this method could be applicable to dehydrogenation of other lower alkanes such as ethane and isobutane, thus contributing to the petrochemical industry's development."

The study is published in Nature Communications.

Explore further

Rh ensemble catalyst for effective automobile exhaust treatment

More information: Nature Communications (2020). DOI: 10.1038/s41467-020-16693-9
Journal information: Nature Communications

Citation: Ultrastable, selective catalyst for propane dehydrogenation developed (2020, June 5) retrieved 6 July 2020 from https://phys.org/news/2020-06-ultrastable-catalyst-propane-dehydrogenation.html
This document is subject to copyright. Apart from any fair dealing for the purpose of private study or research, no part may be reproduced without the written permission. The content is provided for information purposes only.

Feedback to editors

User comments