230 The Power of Hard Rocks: Driving the Energy Transition and Serving Society (Posters)
This session examines how mafic and ultramafic rocks contribute to the energy transition by 1) generating hydrogen gas, 2) trapping CO2 through carbon mineralization, and 3) providing critical minerals for climate change mitigation and renewable energy production.
Tuesday, 21 October 2025
8:00 AM - 5:30 PM
HBGCC, Hall 1
Direct Air Capture of CO2 by Brucite: Effects of Iron and Manganese Doping
Paper number: 230-0
Program: Technical Sessions
Time: 8:00 AM – 8:15 AM
Authors
-
Juliane WeberOak Ridge National Laboratory, Oak Ridge, TN
-
Joanne StubbsUniversity of Chicago GSECARS, Lemont, IL
-
Peter EngUniversity of Chicago GSECARS, Lemont, IL
-
Peter HeaneyPennsylvania State University, State College, PA
-
Andrew StackOak Ridge National Laboratory, Oak Ridge, TN
-
Lawrence AnovitzOak Ridge National Laboratory, Oak Ridge, TN
-
Barbara EvansOak Ridge National Laboratory, Oak Ridge, TN
-
Ke YuanOak Ridge National Laboratory, Oak Ridge, TN
-
Sai AdapaOak Ridge National Laboratory, Oak Ridge, TN
-
Matthew BoebingerOak Ridge National Laboratory, Oak Ridge, TN
-
Michael McGuireOak Ridge National Laboratory, Oak Ridge, TN
-
Raphaël HermannOak Ridge National Laboratory, Oak Ridge, TN
-
George YumnamOak Ridge National Laboratory, Oak Ridge, TN
Abstract
Brucite (Mg(OH)2) is a promising sorbent for direct air capture (DAC) of CO2 because of its availability and low calcination temperatures. However, natural and synthetic brucites tend to contain metal impurities, such as iron or manganese, and the effects of these impurities on CO2 DAC are uncertain. Here, the impact of low concentrations of iron and manganese impurities on the carbonation efficiency of brucite was examined. Brucite with small amounts (1-5 mol%) of Fe and Mn was synthesized. The increasing substitution of Fe into brucite was accompanied by the oxidation of Fe. We suggest that the most plausible location of the impurities in the doped brucites is in the octahedral sites as a substitution for Mg2+. The phase transformation sequence during the carbonation was found to be: brucite → amorphous magnesium carbonate → nesquehonite, regardless of impurity concentration. Both the Fe- and Mn-doped brucite samples were more reactive than endmember brucite, possibly due to their higher surface areas and lower stabilities. During carbonation, 3 mol% Fe- and Mn-doped brucites showed the highest reactivity. The variance in reactivity for Mn-doped brucites was less than that of Fe-doped brucites.
Geological Society of America Abstracts with Programs. Vol. 57, No. 6
doi: 10.1130/abs/2025AM-412946
© Copyright 2025 The Geological Society of America (GSA), all rights reserved. Permission is hereby granted to the author(s) of this abstract to reproduce and distribute it freely, for noncommercial purposes. Permission is hereby granted to any individual scientist to download a single copy of this electronic file and reproduce up to 20 paper copies for noncommercial purposes advancing science and education, including classroom use, providing all reproductions include the complete content shown here, including the author information. All other forms of reproduction and/or transmittal are prohibited without written permission from GSA Copyright Permissions.