In a proposed carbon-capture method, magnesium oxide crystals on the ground bind to carbon dioxide molecules from the surrounding air, triggering the formation of magnesium carbonate. The magnesium carbonate is then heated to convert it back to magnesium oxide and release the carbon dioxide for placement underground, or sequestration. Credit: Adam Malin/ORNL, U.S. Dept. of Energy
Oak Ridge National Laboratory’s research on magnesium oxide for carbon capture reveals a slowing absorption rate over time due to surface layer formation, posing challenges for economic viability and guiding future solution-focused studies.
Magnesium oxide is a promising material for capturing carbon dioxide directly from the atmosphere and injecting it deep underground to limit the effects of climate change. However, making the method economical will require discovering the speed at which carbon dioxide is absorbed and how environmental conditions affect the chemical reactions involved.
Scientists at the Department of Energy’s Oak Ridge National Laboratory (ORNL) analyzed a set of magnesium oxide crystal samples exposed to the atmosphere for decades, and another for days to months, to gauge the reaction rates. They found that carbon dioxide is taken up more slowly over longer time periods because of a reacted layer that forms on the surface of the magnesium oxide crystals.
“This reacted layer is a complicated mix of different solids, which limits the ability of carbon dioxide molecules to find fresh magnesium oxide to react with. To make this technology economical, we are now looking at ways to overcome this armoring effect,” said ORNL’s Juliane Weber, the project’s principal investigator. Andrew Stack, a scientist at ORNL and team member on the project, followed: “If we can do so, this process might be able to achieve the Carbon Negative Energy Earthshot goal of capturing gigaton levels of carbon dioxide from air for less than $100 per metric ton of carbon dioxide.”
Most of the previous research, aimed at understanding how fast the magnesium oxide and carbon dioxide chemical reactions occur, relied on rough calculations rather than materials testing. The ORNL study marks the first time a multidecade test has been conducted to determine the reaction rate over long time scales. Using transmission electron microscopy at the Center for Nanophase Materials Science, or CNMS, at ORNL, the researchers found that a reacted layer forms. This layer consists of a variety of complex crystalline and amorphous hydrated and carbonate phases.
“Additionally, by performing some reactive transport modeling computer simulations, we determined that as the reacted layer builds up, it gets better and better at blocking carbon dioxide from finding fresh magnesium oxide to react with,” ORNL’s researcher Vitaliy Starchenko said. “Thus, going forward, we are looking at ways to bypass this process to allow carbon dioxide to find fresh surface with which to react.”
The computer simulations help scientists and engineers understand how the reacted layer evolves and changes the way in which substances move through it over time. Computer models enable predictions concerning the reactions and movement of materials in natural and engineered systems, such as materials sciences and geochemistry.
Reference: “Armoring of MgO by a Passivation Layer Impedes Direct Air Capture of CO2” by Juliane Weber, Vitalii Starchenko, Ke Yuan, Lawrence M. Anovitz, Anton V. Ievlev, Raymond R. Unocic, Albina Y. Borisevich, Matthew G. Boebinger and Andrew G. Stack, 22 September 2023, Environmental Science & Technology.
DOI: 10.1021/acs.est.3c04690
The DOE Office of Science primarily supported the work. ORNL’s Laboratory Directed Research and Development program supported time-of-flight, or TOF, secondary ion mass spectrometry, or SIMS, and preliminary transmission electron microscopy, or TEM. Atomic force microscopy-TOF-SIMS and TEM characterizations were conducted as part of a user project at the CNMS, a DOE Office of Science user facility at ORNL.
Source: SciTechDaily
