Climate rewind: Scientists turn carbon dioxide
back into coal
February 27, 2019 -- Researchers have used liquid metals to turn carbon dioxide back into solid coal, in a world-first breakthrough that could transform our approach to carbon capture and storage.
“While we can’t literally turn back time, turning carbon dioxide back into coal and burying it back in the ground is a bit like rewinding the emissions clock,” Daeneke, an Australian Research Council DECRA Fellow, said.
Lead author, Dr Dorna Esrafilzadeh, a Vice-Chancellor’s Research Fellow in RMIT’sSchool of Engineering ,
developed the electrochemical technique to capture and convert atmospheric CO2
to storable solid carbon.
February 27, 2019 -- Researchers have used liquid metals to turn carbon dioxide back into solid coal, in a world-first breakthrough that could transform our approach to carbon capture and storage.
The research team led by RMIT University
in Melbourne , Australia , have developed a new
technique that can efficiently convert CO2 from a gas into solid
particles of carbon.
Published in the journal Nature
Communications, the research offers an alternative pathway for safely and
permanently removing the greenhouse gas from our atmosphere.
Current technologies for
carbon capture and storage focus on compressing CO2 into a liquid
form, transporting it to a suitable site and injecting it underground.
But implementation has been
hampered by engineering challenges, issues around economic viability and
environmental concerns about possible leaks from the storage sites.
RMIT researcher Dr Torben
Daeneke said converting CO2 into a solid could be a more sustainable
approach.
“While we can’t literally turn back time, turning carbon dioxide back into coal and burying it back in the ground is a bit like rewinding the emissions clock,” Daeneke, an Australian Research Council DECRA Fellow, said.
“To date, CO2 has
only been converted into a solid at extremely high temperatures, making it
industrially unviable.
“By using liquid metals as a
catalyst, we’ve shown it’s possible to turn the gas back into carbon at room
temperature, in a process that’s efficient and scalable.
“While more research needs
to be done, it’s a crucial first step to delivering solid storage of carbon.”
How the carbon conversion worksLead author, Dr Dorna Esrafilzadeh, a Vice-Chancellor’s Research Fellow in RMIT’s
To convert CO2,
the researchers designed a liquid metal catalyst with specific surface
properties that made it extremely efficient at conducting electricity while
chemically activating the surface.
The carbon dioxide is
dissolved in a beaker filled with an electrolyte liquid and a small amount of
the liquid metal, which is then charged with an electrical current.
The CO2 slowly
converts into solid flakes of carbon, which are naturally detached from the
liquid metal surface, allowing the continuous production of carbonaceous solid.
Esrafilzadeh said the carbon
produced could also be used as an electrode.
“A side benefit of the
process is that the carbon can hold electrical charge, becoming a
supercapacitor, so it could potentially be used as a component in future
vehicles.”
“The process also produces
synthetic fuel as a by-product, which could also have industrial applications.”
The research was conducted
at RMIT’s MicroNano Research Facility and the RMIT Microscopy and Microanalysis
Facility, with lead investigator, Honorary RMIT and ARC Laureate Fellow,
Professor Kourosh Kalantar-Zadeh (now UNSW).
The research is supported by
the Australian Research Council Centre for Future Low-Energy Electronics
Technologies (FLEET) and the ARC Centre of Excellence for Electromaterials Science
(ACES).
The collaboration involved
researchers from Germany (University of Munster ),
China (Nanjing University of
Aeronautics and Astronautics), the US
(North Carolina State
University ) and Australia (UNSW, University
of Wollongong , Monash University ,
QUT).
The paper is published in Nature
Communications (“Room temperature CO2 reduction to solid carbon
species on liquid metals featuring atomically thin ceria interfaces”, DOI:
10.1038/s41467-019-08824-8).
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