Silicate Dissolution Mechanism from Metakaolinite Using Density Functional Theory.

activation energy density functional theory (DFT) dissolution improved dimer method metakaolinite

Journal

Nanomaterials (Basel, Switzerland)
ISSN: 2079-4991
Titre abrégé: Nanomaterials (Basel)
Pays: Switzerland
ID NLM: 101610216

Informations de publication

Date de publication:
27 Mar 2023
Historique:
received: 22 02 2023
revised: 17 03 2023
accepted: 26 03 2023
medline: 14 4 2023
entrez: 13 4 2023
pubmed: 14 4 2023
Statut: epublish

Résumé

Metakaolin (MK) is a high-quality, reactive nanomaterial that holds promising potential for large-scale use in improving the sustainability of cement and concrete production. It can replace cement due to its pozzolanic reaction with calcium hydroxide and water to form cementitious compounds. Therefore, understanding the dissolution mechanism is crucial to fully comprehending its pozzolanic reactivity. In this study, we present an approach for computing the activation energies required for the dissolution of metakaolin (MK) silicate units at far-from-equilibrium conditions using the improved dimer method (IDM) and the transition-state theory (TST) within density functional theory (DFT). Four different models were prepared to calculate the activation energies required for breaking oxo-bridging bonds between silicate or aluminate units. Our results showed that the activation energy for breaking the oxo-bridging bond to a silicate neighbor is higher than that to an aluminate neighbor due to the ionic interaction. However, for complete silicate tetrahedra dissolution, a higher activation energy is required for breaking the oxo-bridging bond to the aluminate neighbor compared to the silicate neighbor. The findings provide methodology for missing input data to predict the mesoscopic dissolution rate, e.g., by the atomistic kinetic Monte Carlo (KMC) upscaling approach.

Identifiants

pubmed: 37049290
pii: nano13071196
doi: 10.3390/nano13071196
pmc: PMC10096740
pii:
doi:

Types de publication

Journal Article

Langues

eng

Subventions

Organisme : Deutsche Forschungsgemeinschaft
ID : 446266595

Références

Nanomaterials (Basel). 2021 Aug 31;11(9):
pubmed: 34578564
Phys Chem Chem Phys. 2022 Dec 21;25(1):455-461
pubmed: 36477563
Phys Rev B Condens Matter. 1994 May 15;49(20):14251-14269
pubmed: 10010505
J Phys Chem A. 2009 Feb 19;113(7):1343-52
pubmed: 19159201
Materials (Basel). 2022 Feb 14;15(4):
pubmed: 35207945
Int J Mol Sci. 2019 Jun 21;20(12):
pubmed: 31234409
Phys Rev B Condens Matter. 1994 Dec 15;50(24):17953-17979
pubmed: 9976227
Materials (Basel). 2023 Feb 24;16(5):
pubmed: 36902975
Phys Rev Lett. 1996 Oct 28;77(18):3865-3868
pubmed: 10062328
Materials (Basel). 2022 Sep 27;15(19):
pubmed: 36234062
J Chem Phys. 2005 Dec 8;123(22):224101
pubmed: 16375464
Materials (Basel). 2022 Sep 14;15(18):
pubmed: 36143700
J Phys Chem A. 2008 Mar 13;112(10):2027-33
pubmed: 18211036
Phys Rev B Condens Matter. 1993 Jan 1;47(1):558-561
pubmed: 10004490
Phys Rev B Condens Matter. 1996 Oct 15;54(16):11169-11186
pubmed: 9984901
Materials (Basel). 2022 Feb 15;15(4):
pubmed: 35207982

Auteurs

Mohammadreza Izadifar (M)

Institute of Construction and Building Materials, Technical University of Darmstadt, Franziska-Braun-Str. 3, 64287 Darmstadt, Germany.

Neven Ukrainczyk (N)

Institute of Construction and Building Materials, Technical University of Darmstadt, Franziska-Braun-Str. 3, 64287 Darmstadt, Germany.

Eduardus Koenders (E)

Institute of Construction and Building Materials, Technical University of Darmstadt, Franziska-Braun-Str. 3, 64287 Darmstadt, Germany.

Classifications MeSH