Metal ion binding by humic substances as emergent functions of labile supramolecular assemblies
Elena A. Vialykh
A E , Dennis R. Salahub B C and Gopal Achari D
+ Author Affiliations
- Author Affiliations
A Department of Chemistry, University of Calgary, 2500 University Drive NW, Calgary, AB T2N 1N4, Canada.
B Department of Chemistry, Centre for Molecular Simulation (CMS), Institute for Quantum Science and Technology and Quantum Alberta (IQST), University of Calgary, 2500 University Drive NW, Calgary, AB T2N 1N4, Canada.
C College of Chemistry and Chemical Engineering, Henan University of Technology, 100 Lian Hua Street, High-Tech Development Zone, Zhengzhou 450001, China.
D Schulich School of Engineering, University of Calgary, 2500 University Drive NW, Calgary, AB T2N 1N4, Canada.
E Corresponding author. Email: elena.vialykh@ucalgary.ca
Environmental Chemistry 17(3) 252-265 https://doi.org/10.1071/EN19198
Submitted: 8 January 2019 Accepted: 19 August 2019 Published: 1 October 2019
Environmental context. The fundamental basis for the high flexibility of humic substances is still unclear, though it is crucial for the understanding of metal bioavailability and toxicity in soil and aqueous environments. We show at the molecular level how characteristics of organic matter affect metal binding depending on the environmental conditions. Such understanding will help in the modulation of metal availability in soil and water in changing environmental situations.
Abstract. In this work, we explore the hypothesis that humic substances (HS) can be perceived as labile supramolecular assemblages, the functioning of which is mainly determined by chemical composition and characteristics, the size of molecular units and weak intermolecular forces, rather than the exact primary structure of molecular moieties and their spatial configuration. To test the hypothesis, 72 computational models of three different organic mixtures were composed. The formation of inner and outer sphere metal–ligand complexes, metal binding sites, complex configurations, binding energies and aggregation/dissolution as emergent properties of HS were determined under various conditions. The results of computational modelling revealed that: (i) the highest Cu2+ binding (55.6 %) was by the SRFA-22 organic model, which represents low-molecular-weight fulvic acids. In contrast, the highest amount of inner-sphere Mg–organic matter complex (63.4 %) was formed in SRHA-6, which has higher-molecular-weight constituents. Therefore, a correlation between the type of cation, the system aromaticity and the extent of metal complexation is proposed. (ii) Increase of metal ion concentration and decrease of water content resulted in an increase in the number of hydrogen bonds and more compact and stable aggregates with lower hydrophilic and higher hydrophobic surface areas in SRFA-22. However, in SRHA-6, the results varied owing to the competition between metal binding, H-bonding and non-polar interactions in the structural arrangement of the aggregates. In general, the aggregation process, driven by metal complexation and water removal, resulted in the formation of more stable conformers, with lower potential energy, with the only exception of SRHA-6–Cu.
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