期刊
EUROPEAN JOURNAL OF MINERALOGY
卷 31, 期 2, 页码 275-287出版社
COPERNICUS GESELLSCHAFT MBH
DOI: 10.1127/ejm/2019/0031-2815
关键词
mineral carbonation; ion solvation; molecular dynamics; ion models; magnesium
类别
资金
- Chinese Scholarship Council
- EPSRC [EP/L000202, EP/P020194/1]
- QMUL Research-IT
- Departments of Chemistry at the University of Hong Kong (China)
- Faculties of Science at the University of Hong Kong (China)
- McMaster University (Canada)
- EPSRC [EP/P020194/1] Funding Source: UKRI
Mineral carbonation (MC) of carbon dioxide (CO2) represents a very promising and long-term solution for the use of captured and stored anthropogenic CO2. One of the potential product of mineral carbonation is magnesite (MgCO3), which is used in a wide range of impacting industrial applications spanning from agriculture to manufacturing. Formed via aqueous carbonation of Mg2+ ions, industrial production is limited by the slow precipitation rates of magnesite; high temperatures and CO2 pressures being a requisite to expedite direct precipitation of anhydrous MgCO3. Research has therefore focused on characterizing and optimizing the fundamental aspects of this slow precipitation under ambient conditions, in order to increase the efficacy and profitability of the process. The principal difficulty arises from the very strong Mg2+ H2O interaction, which raises the barrier for dehydration while hindering nucleation and subsequent growth of Mg-carbonates. Computational modelling, using quantum chemical and molecular dynamic methods, has been used to characterize the structure, energetics, dynamics and kinetics of the Mg2+ (de)hydration process, from the atomic- to meso-scopic scales, employing differing interatomic potentials. Herein, we employ ab initio methods to quantitatively assess several of the currently available Mg2+-ion models. Of these, the Duboue-Dijon parameterised Lennard-Jones models employing Electronic Continuum Correction provide the best agreements with quantum-chemical results, due to models using a +1.5 charge for Mg in lieu of its classically assigned +2.
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